Endangered and Threatened Wildlife and Plants; Determination of Endangered Status for Texas Golden Gladecress and Threatened Status for Neches River Rose-Mallow, 56025-56069 [2013-22085]
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Vol. 78
Wednesday,
No. 176
September 11, 2013
Part V
Department of the Interior
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Fish and Wildlife Service
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Determination of
Endangered Status for Texas Golden Gladecress and Threatened Status
for Neches River Rose-Mallow; Final Rule
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Federal Register / Vol. 78, No. 176 / Wednesday, September 11, 2013 / Rules and Regulations
Executive Summary
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R2–ES–2012–0064;
4500030113]
RIN 1018–AX74
Endangered and Threatened Wildlife
and Plants; Determination of
Endangered Status for Texas Golden
Gladecress and Threatened Status for
Neches River Rose-Mallow
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service, determine
Leavenworthia texana (Texas golden
gladecress) meets the definition of an
endangered species and Hibiscus
dasycalyx (Neches River rose-mallow)
meets the definition of a threatened
species under the Endangered Species
Act of 1973, as amended (Act). This
final rule adds these species to the List
of Endangered and Threatened Plants
and implements the Federal protections
provided by the Act for these species.
DATES: This rule is effective on October
11, 2013.
ADDRESSES: This final rule and other
supplementary information are available
on the Internet at https://
www.regulations.gov (Docket No. FWS–
R2–ES–2012–0064), https://
www.fws.gov/southwest/es/
ElectronicLibrary/ElectronicLibrary_
Main.cfm, or https://www.fws.gov/
southwest/es/ClearLakeTexas/. These
documents, as well as all supporting
information are also available for public
inspection, by appointment, during
normal business hours at, or by
requesting electronic copies from: U.S.
Fish and Wildlife Service, Texas Coastal
Ecological Services Field Office, 6300
Ocean Drive, Unit 5837, Corpus Christi,
TX 78412–5837; by telephone at 361–
994–9005; or by facsimile at 361–994–
8262.
FOR FURTHER INFORMATION CONTACT:
Edith Erfling, Field Supervisor, U.S.
Fish and Wildlife Service, Texas Coastal
Ecological Services Field Office (see
ADDRESSES); by telephone 281–286–
8282; or by facsimile 281–488–5882.
Persons who use a telecommunications
device for the deaf (TDD) may call the
Federal Information Relay Service
(FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
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SUMMARY:
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Why we need to publish a rule. On
September 11, 2012 (77 FR 55968), we
published a proposed rule to list
Leavenworthia texana (Texas golden
gladecress) as an endangered species
and Hibiscus dasycalyx (Neches River
rose-mallow) as a threatened species. In
this rule, we are finalizing our proposed
determinations for these species under
the Act. The Act requires that a final
rule be published in order to add any
plant species to the List of Endangered
and Threatened Plants and to provide
that species protections under the Act.
We are publishing a final rule on the
designation of critical habitat for the
Texas golden gladecress and the Neches
River rose-mallow under the Act
elsewhere in today’s Federal Register.
The critical habitat designation final
rule and its supporting documents will
publish under Docket No. FWS–R2–ES–
2013–0027, and can also be found at the
locations listed in the ADDRESSES
section of this rule.
The basis for our action. Under the
Act, a species may be determined to be
endangered or threatened based on any
of the following five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence.
We have determined that the Texas
golden gladecress meets the definition
of an endangered species due to the
following threats:
• In some cases, a total loss of habitat
and plants, and in others a degradation
of the herbaceous glade plant
communities supporting the Texas
golden gladecress. Activities or factors
that continue to negatively impact the
habitat of the Texas golden gladecress
include glauconite quarrying; natural
gas and oil exploration, production, and
distribution; invasion of open glades by
nonnative and native shrubs, trees, and
vines, and other weedy species; pine
tree plantings in close proximity to
occupied glades; herbicide applications
that have potential to kill emerging
seedlings; and the installation of service
improvements, including water and
sewer lines, domestic gas lines, or
electric lines.
• The inadequacy of existing
regulatory mechanisms to protect the
Texas golden gladecress or its habitats.
• Other natural or manmade factors,
including low numbers of individual
plants and few remaining populations.
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• The above threats are likely
exacerbated by climate change.
We have determined that the Neches
River rose-mallow meets the definition
of a threatened species due to the
following threats:
• Habitat loss and degradation of
open habitats on hydric alluvial soils
along sloughs, oxbows, terraces, and
wetlands of the Neches, Sabine, and
Angelina River basins and Mud Creek
and Tantabogue Creek basins that
support the Neches River rose-mallow.
The Neches River rose-mallow’s habitat
is being lost and degraded by
encroachment of nonnative and native
plant species, particularly trees;
herbicide use; livestock and hog
trampling; and alteration of the natural
hydrology associated with seasonal
flooding to conditions where habitat has
been drained or has become
permanently flooded. Prolonged or
frequent droughts can exacerbate habitat
degradation for both species.
• Inadequacy of existing regulatory
mechanisms to protect the Neches River
rose-mallow or its habitats.
• The above threats are likely
exacerbated by climate change.
Peer review and public comment. We
sought comments from six independent
specialists to ensure that our
designation is based on scientifically
sound data and analyses. We obtained
opinions from four knowledgeable
individuals with scientific expertise to
review our technical assumptions and
analysis, and to determine whether or
not we had used the best available
information. The peer reviewers
generally agreed with portions of our
assessment, including the threats
analysis, and most of our conclusions,
although they pointed out areas where
additional research would refine our
understanding of the two species’
habitat requirements and range. The
peer reviewers pointed out additional
information, clarifications, and
suggestions for future research that
would inform future surveys to refine
the geographic range, and help with
management and recovery efforts.
Information we received from peer
review is incorporated in this final
revised designation. We also considered
all comments and information we
received from the public during the
comment periods.
Previous Federal Actions
On September 11, 2012 (77 FR 55968),
we published a proposed rule to list the
Texas golden gladecress as endangered
and the Neches River rose-mallow as
threatened, both with critical habitat.
On April 16, 2013 (78 FR 22506), we
reopened public comment period on the
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proposed rule. On May 1, 2013, we held
a public hearing to accept oral and
written comments on the proposals.
We are publishing a final rule on the
designation of critical habitat under the
Act (16 U.S.C. 1531 et seq.) for the
Texas golden gladecress and the Neches
River rose-mallow elsewhere in today’s
Federal Register.
Background
Species Information
It is our intent to discuss below only
those topics directly relevant to the
listing of the Texas golden gladecress as
endangered, and the Neches River rosemallow as threatened, in this final rule.
Species information for the Texas
golden gladecress and Neches River
rose-mallow can also be found in the
September 11, 2012 (77 FR 55968),
proposed rule.
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Texas Golden Gladecress
Taxonomy and Description
Texas golden gladecress is a small,
annual, herbaceous plant belonging to
the mustard family (Brassicaceae). Dr.
M. C. Leavenworth, an Army physician,
first collected the taxon in Choctaw
County, Oklahoma, in 1835, and the
specimens were later described as a new
species, Leavenworthia aurea, by Torrey
(Mahler 1981, pp. 76–77).
From 1836 to 1837, Leavenworth
collected similar specimens near the
present-day town of San Augustine, San
Augustine County, Texas, and these
were also identified as L. aurea. E. J.
Palmer (1915 and 1918), and D. S. and
H. B. Correll (1961 to 1962) as cited by
Mahler (1981, pp. 83) made later
collections of the plant in the San
Augustine area. George and Nixon
(1990, pp. 117–127) studied and
mapped populations in this area
between 1979 and 1980. W. H. Mahler
studied the collected specimens and
their habitat, and described the Texas
plants as a new species, Leavenworthia
texana (Mahler 1987, pp. 239–242),
based on differences in morphological
characteristics of flowers and leaves,
and in chromosome number, between
the Oklahoma and Texas plants (Mahler
1987, pp. 239–242).
According to Mahler (1987, p. 240),
Texas golden gladecress flower petals
were a brighter, deeper yellow than
those of L. aurea, and the petals were
egg-shaped and flat instead of being
broad and notched. The L. texana had
wider-than-long terminal leaf segments
that were usually distinctly lobed while
L. aurea’s terminal leaves were
essentially unlobed, flat, and more
circular. Texas plants had a
chromosome number of 2n = 22 (Nixon
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1987, pers. comm. in Mahler 1987, pp.
239, 241) while the Oklahoma L. aurea
had 2n = 48 (Rollins 1963, pp. 9–11;
Beck et al. 2006, p. 156). We are aware
that a recently completed monograph of
the genus may have taxonomic
implications for the Texas and
Oklahoma Leavenworthia species in the
future, but several questions, including
the differences in chromosome number,
remain unresolved and no supporting
information that would change the
current status of Texas golden
gladecress has been published to date
(Poole 2011a, pers. comm.).
Texas golden gladecress is a weakly
rooted, glabrous (smooth, glossy), winter
annual (completes its life cycle in 1
year). Texas golden gladecress is small
in stature, less than 3.9 inches (in) (10
centimeters (cm)) in height, making it
difficult to find except during flowering
or when it bears fruit. The leaves are
0.8–3.1 in (2–8 cm) long and 0.4–0.6 in
(1–1.5 millimeters (mm)) wide, forming
rosettes at the base of the plant.
Terminal leaf segments are wider-thanlong, and usually distinctly lobed, with
angular teeth. Flowers are bright yellow
and borne on scapes (leafless flowering
stems or stalks arising from the ground)
that are 1.2–3.5 in (3–9 cm) long early
in the flowering season. Later in the
season, the flowers occur on
unbranched flower clusters that come
off a single central stem from which the
individual flowers grow on small stalks,
at intervals. The four petals are bright
golden-yellow with a slightly darker
base, narrowly obovate (tongue-shaped),
0.3–0.4 in (7–10 mm) long and 0.1–0.2
(3.5–5 mm) wide. The fruit is a slender
seed capsule, known as a silique, with
a length (0.6–1.2 in (15–30 mm)) that is
more than twice its width (0.08–0.22 in
(2–5.5 mm)) and that contains 5 to 11
flattened, circular or spherically shaped
seeds. The description above was drawn
from Poole et al. (2007, p. 286), who
adapted it from others.
Habitat
Texas golden gladecress occurs within
the Pineywoods natural region of
easternmost Texas, within the Gulf
Coastal Plain Physiographic Region. The
region is defined by uplands that are
forested by pine dominated woodlands,
interspersed with bottomland, mesic
slope, and bald cypress-tupelo swamp
forests. Water oak and willow oak are
prominent in the large stream
floodplains, while some ancient sloughs
are fringed by planer tree and overcup
oaks (Dolezel 2012, pers. comm.). Many
of the rare plants of the Pineywoods
region, including the Texas golden
gladecress and the federally endangered
Lesquerella pallida (=Physaria pallida)
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(white bladderpod) are found in smallscale plant communities tied to
‘‘geologic and hydrologic conditions
that are themselves rather rare on the
landscape’’ (Poole et al. 2007, p. 6).
Based on all documented occurrence
records, the Texas golden gladecress is
endemic to glade habitats in northern
San Augustine and northwest Sabine
Counties, Texas, where it is a habitat
specialist, occurring only on outcrops of
the Weches Geologic Formation (Mahler
1987, p. 240; George and Nixon 1990, p.
120; Poole et al. 2007, pp. 286–287).
The gladecress grows only in glades on
shallow, calcium-rich soils that are wet
in winter and spring. These occur on
ironstone (glauconite or green-stone)
outcrops (Poole et al. 2007, p. 286).
All species within the small genus
Leavenworthia share an adaptation to
glade habitats that have unique physical
characteristics, the most important
being a combination of shallow soil
depth and high calcium content
(dolomitic limestone or otherwise
calcareous soils) where the soil layers
have been deposited in such a manner
that they maintain temporary highmoisture content at or very near the
surface (Rollins 1963, pp. 4–6).
Typically, only a few inches of soil
overlie the bedrock, or, in spots, the soil
may be almost lacking and the surface
barren. Within the Weches Formation
glades, gladecress habitat occurs on thin
soils that overlie calcium-rich parent
materials where the calcium is derived
from a myriad of fossilized, calciumdominated oyster shells and other
marine life (Dolezel 2012, pers. comm.,
p. 1).
The glade habitats that support all
Leavenworthia species are extremely
wet during the late winter and early
spring and then dry to the point of being
parched in summer (Rollins 1963, p. 5).
These glades can vary in size from as
small as a few meters to larger than 0.37
square miles (mi2) (1 square kilometer
(km2)) and are characterized as having
an open, sunny aspect (lacking canopy)
(Quarterman 1950, p. 1; Rollins 1963, p.
5). The landscape position of the glades
may also play a role in assuring the
cyclic moisture regime required by
glade vegetation communities.
The Weches Geologic Formation
consists of Eocene-age deposits that lie
mostly in an east-west band of ancient
marine sediments. These sediments
were deposited in a line roughly parallel
to the Gulf of Mexico, running from
Sabine to Frio Counties, Texas. The
Weches Formation also extends over
100 miles to the north of Nacogdoches
County into Smith, Wood, Upshur,
Marion, and Cass Counties, Texas, and
even into Miller County, Arkansas
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(Godwin 2012, pers. comm., p. 2). A
layer of glauconite clay is either
exposed at the surface or covered by a
thin layer of calcareous (calciumcontaining) sediment measuring as deep
as 20 in (50 cm) (George and Nixon
1990, pp. 117–118). Glauconite is a
characteristic mineral of marine
depositional environments, presenting a
greenish color when initially exposed to
the atmosphere, and later turning red
(Davis 1966, pp. 17–18; Nemec 1996, p.
7). The area of the Weches outcrops in
San Augustine County is referred to as
the ‘‘redlands’’ (Ritter 2011b, pers.
comm.). The glauconite is very friable
(crumbly) and has low resistance to
weathering (Geocaching.com 2010, p. 5).
The soils overlying the clay layer are
typically rocky and shallow (George
1987, p. 3) and at all Texas golden
gladecress sites are classified within the
Nacogdoches, Trawick, or Bub soils
series (United States Department of
Agriculture 2009, entire).
Within the known range of the Texas
golden gladecress, Weches outcrops
occur in a band averaging 5 miles (mi)
(8 kilometers (km)) in width that
parallels Texas State Highway (SH) 21
through northern San Augustine and
northwestern Sabine Counties (Sellards
et al. 1932 in Diggs et al. 2006, p. 56).
It has been deeply dissected by erosion
that created islands of thin, loamy,
alkaline soils (pH 7–8), within the
normally deep, sandy, acidic soils (pH
4–5) of the Pineywoods region. The
glauconite layer of the Weches
Formation is fairly impermeable to
water, producing saturated, thin upper
soils in late fall through spring, that dry
out and harden during summer months
(George 1987, pp. 2–4; Bezanson 2000 in
Diggs et al. 2006, p. 56). Down-slope
seepage across the Weches terraces may
also be important to maintain the
hydrology required by the gladecress
(Singhurst 2003, pers. comm.). The
cyclic moisture regime and the
alkalinity of the soils produce
conditions unique to the Weches
outcrops. Certain plants, such as the
Texas golden gladecress, have evolved
to live within these specialized geologic
formations (Mahler 1987, p. 240; George
and Nixon 1990, pp. 120–122).
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Biology
The Texas golden gladecress occurs in
open, sunny, herbaceous-dominated
plant communities in Weches glades, in
some areas that also support the white
bladderpod (Bridges 1988, pp. II–7, II–
35, and II–35 supplement). Unlike the
white bladderpod, which can grow
throughout the glade, the gladecress is
restricted to the outcrop rock faces
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within the glades where it occurs
(Nemec 1996, p. 8).
As is true of other Leavenworthia
species (Rollins 1963, p. 6), Texas
golden gladecress seeds germinate
during fall rains and the plants
overwinter as small, tap-rooted rosettes.
Flowering begins in February and
continues into March, and sometimes as
late as April, depending on annual
weather conditions. Rollins (1963, p. 6)
noted that the blooming period of
Leavenworthia varied according to the
temperature, moisture, and severity of
winter freezes. Fruit production is
generally seen from March into April.
The plants respond to drying of the soil
by dropping seed and withering away,
usually in April and May (Singhurst
2011b, pers. comm.). By summer
months, gladecress plants are dead,
replaced by other low-growing species
such as Sedum pulchellum (stonecrop),
Portulaca oleracea (common purslane),
Phemeranthus parviflorus (sunbright),
and Eleocharis occulata (limestone
spikerush) (Singhurst 2012e, pers.
comm.). Although seed dispersal has
not been studied in Texas golden
gladecress, observations indicate that
seeds fall within 6–8 in (15–20 cm) of
the parent plant (Singhurst 2011c, pers.
comm.).
Little is known about the Texas
golden gladecress’s seed bank as this
aspect of life history has not been
researched. The species did reappear at
two sites where it was believed lost due
to habitat degradation. A population
location, the Geneva Site in Sabine
County, was bulldozed in late March
1999, one week after flowering plants
were counted; the site was subsequently
described by the surveyor as ‘‘lost or
destroyed’’ (Turner 1999, pers. comm.).
However, plants were found again at
this site in 2003, and continued to
emerge in succeeding years. At a second
site in San Augustine County (Chapel
Hill Site) a thick growth of the invasive,
nonnative shrub, Rosa bracteata
(Macartney rose) was removed in 1995.
Post-brush removal, the Texas golden
gladecress reappeared after not having
been seen for the previous 10 years
(Nemec 1996, p. 1). The species’
reappearance after these habitat
alterations suggests a persistent seed
bank, although there have been no
formal studies to verify this hypothesis.
Rare plants often have adaptations
such as early blooming, extended
flowering, or mixed-mating systems that
allow them to persist in small
populations (Brigham 2003, p. 61). The
Texas golden gladecress is believed to
be self-compatible and able to selffertilize (Rollins 1963, p. 19; Beck et al.
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2006, p. 153). The species may have
evolved for self-fertilization when
conditions are not favorable for insectvectored pollination, lessening the
species’ dependence on pollinators for
cross-pollination and survival and
potentially making the species more
resilient under conditions of small,
geographically separated populations.
Rollins (1963, pp. 41–47) speculated
that species in the genus Leavenworthia
evolved from a self-incompatible
original ancestor to self-compatibility in
some species to persist with a
diminishing overlap in seasonality of
adequate moisture in glade habitats
versus availability of insect pollinators
(e.g., as the southeastern part of the
United States warmed, the required
moisture levels for germination and
flowering became more restricted to
winter months when insect availability
was lower). This could help to enhance
the species’ persistence, at least in the
short term, in a fragmented landscape
where habitat patches may be so distant
from one another as to preclude
pollinators’ movements between them.
Even so, the presence of other flowering
plants at gladecress sites could help to
attract and maintain a reservoir of
potential pollinators, thereby increasing
the chances for the gladecress to be
cross-pollinated. This would benefit the
species by potentially providing, or
maintaining, a higher level of genetic
diversity.
Distribution and Status
Texas golden gladecress is known
from eight locations (historic and
extant), including one introduced
population, all within a narrow zone
that parallels SH 21 in San Augustine,
Sabine, and Nacogdoches Counties
(Texas Natural Diversity Database
(TXNDD) 2012b). Table 1 (below)
summarizes the location information for
Texas golden gladecress populations
(taken from the TXNDD 2012b). Based
on known population locations, taken
from the TXNDD element occurrence
records from 1974–1988, the Weches
glades of San Augustine County appear
to be the center of the species’
distribution; to date all but one of the
naturally occurring populations were
found in this area, with the other
naturally occurring population in
Sabine County. One population was
successfully introduced into
Nacogdoches County. All locations
(historic and extant) occur primarily on
privately owned land, although the
plants do extend onto the Texas
Department of Transportation (TXDOT)
right-of-way (ROW) at two sites: Geneva
Site and Caney Creek Glade Site 1.
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TABLE 1—LOCATION AND STATUS OF TEXAS GOLDEN GLADECRESS POPULATIONS
County
Population designation
Status
Historic site description
San Augustine ...........
Caney Creek Glade Site 1 ...
Extant ....................................
Private & State ROW.
San Augustine ...........
Chapel Hill (also known as
Tiger Creek).
Extant ....................................
Sabine ........................
Geneva .................................
Extant ....................................
Nacogdoches .............
Simpson Farms (introduced
population).
San Augustine ...........
Caney Creek Glade Site 7 ...
Caney Creek Glade Site 2 ...
Caney Creek Glade Site 6 ...
San Augustine ...........
Caney Creek Glade Site 8 ...
Small population; locally
abundant in very small
area.
Site was ∼ 3 ac (1.21 ha) .....
Multiple tracts totaling ∼ 10
ac. Sites 6, 7, and 8 in different areas on these
tracts. Site 6 was the largest known population
(thousands of plants).
Very small population on a
degraded outcrop.
Private.
San Augustine ...........
San Augustine ...........
Extant through 2009. Site
was eradicated by pipeline
in 2011.
Status unknown. Possibly
extant—not accessible in
last 24 years.
Site is now excavated pits ....
Site is now excavated pits.
Possibility that some habitat and plants remain on
adjacent, unquarried land.
By 2001, was less than 100
ft2 (9 m2).
Tract on which Texas golden
gladecress was found was
less than 0.25 ac (0.1 ha).
Size of site was ∼ 100 ft2 (9
m2).
Population ∼ 200 ft2 (18 m2)
in size.
Four Texas golden gladecress
populations (Caney Creek Glade 1,
Chapel Hill, Geneva, and Simpson
Farms) were present through 2009, the
last year that the plants were surveyed
and counted (Singhurst 2011a, pers.
comm.). In October 2011, Service and
Texas Parks and Wildlife Department
(TPWD) biologists visited all four
known locations and found that the
plants and habitat at the introduced site
in Nacogdoches County (Simpson
Farms) had been removed by a recent
pipeline installation. The habitat was
still intact at the other three locations in
October 2011 (Cobb 2011, pers. comm.),
and the presence of the plants
themselves was subsequently observed
at the three accessible sites in February
2012 (Singhurst 2012f, p. 1).
Three San Augustine County
occurrences (Caney Creek Glade Sites 2,
6, and 8) were believed extirpated, at
least in large part, by construction of
glauconite mines (open pits) beginning
in the late 1990s. These occurrences
may have been part of a much larger
glade complex, referred to as the Caney
Creek Glade Complex, that included the
Caney Creek Glade Sites 1, 2, 6, 7, and
8. These five occurrences were located
within an area extending out to 1.5 mi
(2.41 km) to the east of the town of San
Site lost to excavated pits ....
Augustine (TXNDD 2012b,
unpaginated). In 1987, the Caney Creek
Glade Site 6 was described as having
Texas golden gladecress plants ‘‘in the
thousands’’ (TXNDD 2012b,
unpaginated). Access to these three
privately owned sites is prohibited;
therefore, we cannot ascertain whether
any plants or their habitat are still
present on the peripheries of the mined
areas.
For Caney Creek Glade Site 7, the last
TXNDD (2012b, unpaginated) element
of occurrence record was from 1988, a
time when the presence of Texas golden
gladecress was confirmed at the site.
The site was visited by a forestry
consultant in 1996, who described the
glade as being intact at that time. This
individual revisited the site in 2000,
and found invasive woody plants
encroaching into the glade (Walker
2012, p. 4). There were no further site
visits due to lack of access to this
privately owned tract. Satellite images
taken as recently as 2008 show this site
has not been altered by construction or
quarrying (mining), but the open glade
appearance at this site has changed to
one of dense growth of woody
vegetation, so it is unknown whether
the plants still occur at the site.
Land owner
Private.
Private & State ROW.
Private.
Private.
Private.
Private.
Table 2 presents estimates for extant
Texas golden gladecress populations
between 1999 and 2009 (Service 2010a,
p. 4). The total number of plants seen
in 2009 was 1,108. The largest
population, consisting of 721 plants,
was at the introduced site in
Nacogdoches County, a site that was lost
in 2011, when a pipeline route was
constructed through it. This represents
a loss of 65 percent of the known plants.
After 2009, approximately 400 plants in
three populations were all that
remained of this species. The number of
Texas golden gladecress plants
fluctuated widely from year to year,
likely due to differences in precipitation
levels between years. The Texas golden
gladecress is dependent on fall and
winter rain to saturate the sediment and
produce the seeps and pooling it
requires, and drought conditions were
noted to have a significant negative
effect on reproduction (Turner 2000, p.
1) as seen in the drought years of 1999–
2000 (Texas Water Resources Institute
2011, unpaginated) when the Chapel
Hill site decreased from 91 to 67 plants
and the Caney Creek Glade Site 1
decreased from 490 to 96 plants (Service
2010a, p. 5).
mstockstill on DSK4VPTVN1PROD with RULES2
TABLE 2—POPULATION ESTIMATES FOR TEXAS GOLDEN GLADECRESS AT MONITORED SITES
Chapel
Hill
Year
1999 .........................................................................................................................................................
2000 .........................................................................................................................................................
2001 .........................................................................................................................................................
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91
67
96
11SER2
Caney
Creek
Glade 1
Geneva
Simpson
Farms
490
96
520
319
NS
NS
*NS
NS
270
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TABLE 2—POPULATION ESTIMATES FOR TEXAS GOLDEN GLADECRESS AT MONITORED SITES—Continued
Chapel
Hill
Year
2002
2003
2004
2005
2006
2007
2008
2009
.........................................................................................................................................................
.........................................................................................................................................................
.........................................................................................................................................................
.........................................................................................................................................................
.........................................................................................................................................................
.........................................................................................................................................................
.........................................................................................................................................................
.........................................................................................................................................................
NS
42
NS
40–50
NS
200
9
98
Caney
Creek
Glade 1
Geneva
Simpson
Farms
NS
NS
NS
0
NS
NS
NS
29
NS
57
NS
54
200
1,000
49
260
NS
57
NS
2,873
NS
1,000
NS
721
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* NS—Not surveyed.
Singhurst (2011a, pers. comm.)
referred to the difficulty of trying to
determine population trends for the
Texas golden gladecress due to the lack
of comprehensive numbers for the
species. He attributed this data gap to
variation in surveyors and their
techniques, the inability to see Texas
golden gladecress plants under invasive
brush, lack of access to multiple sites,
and the fluctuation in plant numbers
associated with moisture conditions.
Nevertheless, despite these limitations,
it is evident that there are few remaining
populations and that the overall
numbers of existing plants are
fluctuating. For example, a decrease in
plant numbers in 2009 (Singhurst 2009,
p. 1) was likely due to drought;
however, following significant rains in
late fall 2011 and early winter 2012,
Singhurst (2012f, pers. comm.) noted
higher numbers of plants than the 2009
counts at Geneva, Chapel Hill, and
Caney Creek Glade Site 1.
Most of the known populations,
historic and extant, were and are
restricted to small areas (see Table 1).
For example, in San Augustine County,
the Chapel Hill site is less than 0.2 acres
(ac) (0.1 hectare (ha)) in size and lies
between a pasture fence and gravel road
southwest of SH 21. The area of the
plants at the Caney Creek Glade Site 1
is less than 100 feet squared (ft2) (9
meters squared (m2)) in size, on the side
of Sunrise Road south of SH 21. In
Sabine County, the plants at the Geneva
site occupy approximately 100 ft2 (9 m2)
adjacent to, and west of, SH 21, south
of Geneva. The total area occupied by
the plants at the remaining three sites
covers less than 1.2 ac (0.5 ha). Area
sizes for Texas golden gladecress
occurrences were taken from the
TXNDD element of occurrence records.
Although no new populations of
Texas golden gladecress have been
found since the late 1980s, there is
potential for more Texas golden
gladecress to exist across the Weches
glades region. Known populations all
occur close to roads, suggesting that
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most searches for the species were
nearby to public road access. All known
occurrences are on private property, as
is all remaining habitat, and surveys
cannot be conducted without landowner
permission. Effective identification of
suitable habitat is needed to survey for
new populations. Even in areas of
potential Weches glades, as identified
using Geographic Systems Information
(GIS) data, including aerial, geologic,
and hydrologic data sources, the habitat
may not contain Texas golden
gladecress populations. Between 1999
and 2003, The Nature Conservancy
(TNC) used these tools to identify 44
potential sites of Texas golden
gladecress and white bladderpod
occurrence in the San Augustine glades.
The San Augustine glades were
delineated by TNC as a subset of the
Weches glades for purposes of
developing an area conservation plan.
The San Augustine glades are located in
north-central and northeastern San
Augustine County. TNC was granted
access to 14 of the 44 sites, but found
little Weches glade habitat, and no new
Texas golden gladecress or white
bladderpod sites (Turner 2003, in
Service 2010a, p. 3).
Conservation
The Texas golden gladecress was
included as a nested element within the
Coastal Plain Carbonate Glades
conservation element of the San
Augustine Glades Area Conservation
Plan developed by TNC of Texas in
2003 (TNC 2003, entire). This plan was
envisioned to provide guidance for the
conservation and restoration of a
network of ecologically functional
forests and glades along the Weches
Geological Formation in San Augustine
County. The plan was generated through
TNC’s structured conservation planning
process, which relied on a science team
with expertise in east Texas flora and
habitats, including members from
academia, botanical institutions, and
Federal and State agencies. The
conservation planning process
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concluded that at least 8 viable (selfsustaining, ecologically functioning)
populations of Texas golden gladecress,
containing an average of 500 individual
plants each, at least 1 out of every 5
years, was the target conservation goal
for the species (TNC 2003, pp. 8, 12).
Neches River Rose-Mallow
Taxonomy and Description
Hibiscus dasycalyx (Neches River
rose-mallow) (Blake and Shiller) is a
nonwoody perennial (plant that grows
year after year) in the Malvaceae
(mallow) family that grows 1.9–7.5 feet
(ft) (0.6–2.3 meters (m)) tall (Correll and
Johnston 1979, p. 1030). Leaves are
alternate and simple, generally t-shaped
and deeply three-lobed with petioles
(leaf stalks) 1.1–1.9 in (3–5 cm) long
(Correll and Johnston 1979, p. 1030).
The Neches River rose-mallow generally
produces a single creamy white (rarely
pink) flower at the base of the leaf stalks
along the uppermost branches or stems
(Blanchard 1976, pp. 27–28; Warnock
1995, p. 2; Poole et al. 2007, pp. 264–
265). Because the plants are single to
multi-stemmed and each branch or stem
can have numerous leaves, the total
number of flowers per plant can number
in the hundreds (Poole 2013b, pers.
comm.). Flowering occurs between June
and August (Poole et al. 2007, p. 265),
sometimes into late October depending
on water availability during springtime
inundations (Warnock 1995, p. 20;
Center for Plant Conservation 2011).
Large and numerous stamens are
monodelphous, forming a tube that is
united with the base of the petals (Klips
1999, p. 270).
The Neches River rose-mallow was
first collected by Ivan Shiller on June
23, 1955, at the type locality at SH 94
(also referred to as Apple Springs),
Trinity County, Texas, and it was later
recognized it as a distinct species
(Correll and Johnston 1979, pp. 1030–
1031). Blake (1958, p. 277) determined
that the Neches River rose-mallow was
different from the closely related
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Hibiscus laevis (halberdleaf rosemallow) by examining specimens from
the type locality. Gould (1975), Nixon
(1985), Hatch et al. (1990), Johnston
(1990), and Fryxell (all in Warnock
1995, pp. 1–2; Poole 2002, pers. comm.)
all recognized the Neches River rosemallow as a distinct species.
Two similar-looking Hibiscus species,
H. laevis (halberdleaf rose-mallow) and
H. moscheutos (crimsoneyed or wooly
rose-mallow) are wetland species
documented in areas where the Neches
River rose-mallow occurs. All three of
these species have a similar general
appearance, but can be separated based
on a comparison of external
characteristics including leaf structure,
and degree of pubescence (fine hairs) on
the calyx, leaves, capsule (dry fruit), or
seeds (Correll and Correll 1975, p. 1118;
Blanchard 1976, p. 5; Warnock 1995, p.
4). Similar to H. moscheutos, the Neches
River rose-mallow has a hairy calyx but
with larger, spreading hairs rather than
a covering of small, short hairs
(Warnock 1995, pp. 2–3).
Geographically, these three species can
be found within similar habitats, but the
halberdleaf and the crimsoneyed rosemallows prefer areas near deeper water
and are found along edges of major
rivers and streams (Blanchard 1976, pp.
10–14; Poole 2011b, pers. comm.),
compared with the Neches River rosemallow, which is found in side
channels and floodplains of major river
drainages. Based on the best scientific
and commercial data available on the
species’ morphology, biology, and
habitat-specific needs, we conclude that
the Neches River rose-mallow is a valid
taxon.
Habitat
The Neches River rose-mallow is
endemic to the relatively open habitat
(Kennedy and Poole 1990, p. 11) of the
Pineywoods (or Timber belt) of east
Texas (Gould 1975, p. 1; Correll and
Johnston 1979, p. 1030), within
Cherokee, Houston, Harrison, and
Trinity Counties, and has been
introduced into Nacogdoches and
Houston Counties. Shortleaf-loblolly
pine-hardwood forests, longleaf pine
(Pinus palustris), and loblolly pine
forest (Pinus taeda) dominate the
Pineywoods vegetation region (Telfair
1983, p. 29; Diggs et al. 2006, p. 6). More
specifically, Neches River rose-mallow
is found within seasonally flooded river
floodplains as described by Diggs et al.
(2006), where the natural bottomlands
occupy flat, broad portions of the
floodplains of major rivers and are
seasonally inundated. Loamy to clayey
soils seasonally flood and host floodtolerant species of Quercus sp. (oak),
Liquidambar styraciflua (sweetgum),
Ulmus americana (American elm),
Nyssa biflora (swamp tupelo), and Acer
rubrum (red maple) (Diggs et al. 2006,
p. 103). Bottomland and floodplain
areas may be dominated by Q. lyrata
(overcup oak). Stands of shortleaf,
longleaf, and loblolly pine are not
occupied by the Neches River rosemallow. The common native woody and
herbaceous plant associates are listed in
Table 3 (Warnock 1995, pp. 14–15;
Poole et. al 2007, pp. 264–265).
TABLE 3—NATIVE PLANT ASSOCIATES OF NECHES RIVER ROSE-MALLOW
Scientific name
Common name
Native Woody Plant Associates
Carya aquatica .........................................................................................
Cephalanthus occidentalis ........................................................................
Celtis laevigata var. laevigata ..................................................................
Fraxinus sp ...............................................................................................
Quercus lyrata ..........................................................................................
Q. nigra .....................................................................................................
Liquidambar styraciflua .............................................................................
Salix nigra .................................................................................................
water hickory.
common buttonbush.
sugar berry.
ash.
overcup oak.
wateroak.
sweetgum.
black willow.
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Native Herbaceous Plant Associates
Boehmeria cylindrica ................................................................................
Brunnichia ovata .......................................................................................
Carex lupulina ...........................................................................................
Chasmanthium sessilifolium .....................................................................
Diodia virginiana .......................................................................................
Eichhornia crassipes ................................................................................
Heliotropium indicum ................................................................................
Hibiscus moscheutos ................................................................................
H. moscheutos ..........................................................................................
H. laevis (= H. militaris) ............................................................................
Hydrolea ovata .........................................................................................
Hydrocotyle ranunculoides .......................................................................
Juncus effusus ..........................................................................................
Ludwigia leptocarpa ..................................................................................
Nuphar lutea .............................................................................................
Phanopyrum gymnocarpon ......................................................................
Panicum rigidulum ....................................................................................
Pluchea foetida .........................................................................................
Polygonum hydropiperoides .....................................................................
Pontederia cordata ...................................................................................
Rhynchospora corniculata ........................................................................
Sesbania herbacea ...................................................................................
Scirpus cyperinus .....................................................................................
Thalia dealbata .........................................................................................
Trachelospermum difforme .......................................................................
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smallspike false nettle.
buckwheat vine.
common hop sedge.
longleaf woodoats.
Virginia buttonweed.
water hyacinth.
Indian heliotrope.
crimsoneyed rose-mallow.
wooly rose-mallow.
halberdleaf rose-mallow.
ovate false fiddleleaf.
floating pennywort.
common rush.
anglestem primrose-willow.
yellow pond-lily.
Savannah-panicgrass.
redtop panicgrass.
stinking camphorweed.
swamp smartweed.
pickerelweed.
shortbristle horned beaksedge.
bigpod sesbania.
woolgrass.
powdery alligator-flag.
climbing dogbane.
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Sites where the Neches River rosemallow has been found have been
described as sloughs, oxbows, terraces,
and sand bars. Sites are seasonally
inundated or regularly flooded
bottomlands (Diggs et al. 2006, p. 103)
that include low areas (Warnock 1995,
p. 13) within the Neches, Sabine, and
Angelina River basins and Mud and
Tantabogue Creek basins. Soils are
classified generically as hydric alluvials
(water-saturated soils) of the Inceptisol
or Entisol orders (Diggs et al. 2006, pp.
46, 79) and although generally watersaturated, can often be surficially dry.
The U.S. Department of Agriculture’s
(USDA) Natural Resources Conservation
Service (NRCS) completed soils surveys
for all counties with known occurrences
of the Neches River rose-mallow, and
the associated soils are frequently
flooded clay loams. Sites are both
perennial and intermittent wetlands
with water levels between sites varying
due to their proximity to water, amount
of rainfall, and floodwaters. Intermittent
wetlands are inundated during the
winter months but become dry during
the summer months (Warnock 1995, p.
11). Warnock (1995) noted that seed
dispersal is likely by water, and Scott
(1997, p. 5) also stated that seed
dispersal appears to be entirely water
dependent. While water-mediated seed
dispersal of the Neches River rosemallow is highly likely, it is not known
that flowing water is required for
downstream dispersal of rose-mallow
seeds. Rivers of east Texas tend to
overflow onto banks and floodplains
(Diggs et al. 2006, p. 78), especially
during the rainy season, thereby
dispersing seed. Research has not been
done to identify methods of seed
dispersal upstream; however, avian
species may facilitate this process.
mstockstill on DSK4VPTVN1PROD with RULES2
Biology
The Neches River rose-mallow is a
perennial that dies back to the ground
every year and resprouts from the base;
however, the plant still maintains
aboveground stems. Longevity of the
species is unknown, but it may be longlived. Cross-pollination occurs
(Blanchard 1976, p. 38) within the
Neches River rose-mallow populations,
and the species has high reproductive
potential (fecundity). The number of
flowers and fruits per plant were
documented during the TPWD’s annual
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monitoring of the Neches River rosemallow along SH ROWs. The species
produced an average of 50 fruits per
plant, but seed viability and
survivorship are not known (Poole
2012a, pers. comm.). An open canopy is
typical within Neches River rosemallow habitat (Warnock 1995, pp. 11,
13), but plants also grow in partial sun
(as is the case at SH 204). Sunlight is
needed for blooming, as the blooming
period may only last 1 day (Snow and
Spira 1993, p. 160).
Potential pollinators of the Neches
River rose-mallow may include, but are
not limited to, the common bumblebee
(Bombus pensylvanicus), Hibiscus bee
(Ptilothrix bombiformis), moths, and the
scentless plant bug Niesthrea
louisianica (Klips 1995, p. 1471;
Warnock 1995, p. 20; Warriner 2011,
pers. comm.). Both Hibiscus laevis and
H. moscheutos are pollinated by
common bumblebees and the Hibiscus
bee (Snow and Spira 1993, p. 160; Klips
1999, p. 270). The solitary Hibiscus bee
prefers gently sloping or flat areas with
sandy or sandy-loam soils for nesting
areas (Vaughan et al. 2007, pp. 25–26;
Black et al. 2009, p. 12), and female bees
will excavate nest cavities in elevated,
hard packed dirt roadways or levees
near stands of Hibiscus (in this case H.
palustris) and standing water (Rust
1980, p. 427). Members of the genus
Bombus (family Apidae) are social bees,
predominantly found in temperate
zones, nesting underground (Evans et al.
2008, p. 6) in sandy soils (Cane 1991, p.
407). Bumblebees nest in small cavities,
often underground in abandoned rodent
nests, in grass (Black et al. 2009, p. 12),
or in open, grassy habitat (Warriner
2012a, pers. comm.). Other
aboveground-nesting bees that may
potentially pollinate the Neches River
rose-mallow may include carpenter,
mason, and leaf cutter bees that nest in
dead snags or twigs or standing dead
wood (Warriner 2012a, pers. comm.).
Maximum foraging distances of solitary
and social bee species are 492 to 1,968
ft (150 to 600 m) (Gathmann and
Tscharntke 2002, p. 762) and 263 to
5,413 ft (80 to 1,650 m) (WaltherHellwig and Frankl 2000, p. 244),
respectively. The scentless plant bug is
a member of the Rhopalidae family
found specifically in association with
various members of the Malvaceae
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family. This species is known to deposit
eggs on both the vegetative and
reproductive parts of mallow plants
(Spencer 1988, p. 421). Holes have been
eaten in floral parts of Neches River
rose-mallow plants, suggesting that the
scentless plant bug may be a pollinator
as well as a consumer of the Neches
River rose-mallow.
Natural fires occurred every 1 to 3
years in east Texas (Landers et al. 1990,
p. 136; Landers 1991, p. 73) and
controlled the overgrowth of longleaf
and loblolly pine, as well as nonnative
species. In more recent history, humans
used fire to suppress overgrowth. Fire
suppression allows for sweetgum, oaks,
Carya sp. (hickories), Diospyros
virginiana (common persimmon), and
Magnolia grandiflora (southern
magnolia) to invade the natural pine
forests (Daubenmire 1990, p. 341;
Gilliam and Platt 1999, p. 22), and
reduce the open canopy needed by the
Neches River rose-mallow. Lack of fire
increases the opportunity for nonnative
species, such as Triadica sebifera
(Chinese tallow), to invade these sites.
Distribution and Status
The natural geographic range of the
Neches River rose-mallow is within
Trinity, Houston, Harrison, and
Cherokee Counties, Texas, on SH ROWs
and on private and Federal lands.
However, the species has been
introduced outside of the known
geographic range in Nacogdoches
County on private land (Mill Creek). In
addition, populations of Neches River
rose-mallow have been introduced
within their natural geographic range on
Federal lands in Houston County. In
total, there are 12 occurrences of Neches
River rose-mallow (see Table 4).
However, only 11 of these are within the
known geographic range and, as of
October 2011, are considered occupied
by the Neches River rose-mallow. The
Neches River rose-mallow plants within
the SH 230 ROW have not been seen
since 2002, and the site was considered
extirpated. In 2011, Neches River rosemallow plants were not located at this
site, but in 2012, a graduate student
from Stephen F. Austin State University
reported seeing the Neches River rosemallow along SH 230 in the ROW
somewhere near the former site
(Melinchuk 2012, p. 3).
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56033
TABLE 4—POPULATION ESTIMATES FOR KNOWN NECHES RIVER ROSE-MALLOW OCCURRENCES
County
First and last
observation
Plant estimates
(or otherwise noted)
1. Compartment 55, Davy Crockett National Forest (NF).
Houston ............
2002–2003; 2011
2. Compartment 16, Davy Crockett NF (introduced).
Houston ............
2000; 2011
3. Compartment 11, Davy Crockett NF (introduced).
4. Compartment 20, Davy Crockett NF (introduced).
Houston ............
2004; 2011
Houston ............
2000; 2011
5. SH 94 ROW-Boggy Slough ......
Trinity ................
1955; 2011
6. SH 204 ROW-Mud Creek .........
Cherokee ..........
1992; 2011
7. SH 230 ROW ............................
Houston ............
1978; 2002
8. Lovelady ....................................
Houston ............
2011
9. Mill Creek Gardens (introduced)
10. Harrison Site ...........................
Nacogdoches ...
Harrison ............
11. Champion site .........................
12. Camp Olympia ........................
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Site
Trinity ................
Trinity ................
1995; 2011
Not observed after
1980
1996; 2001
1977; 1978
750 in 2002; 500 in 2005; 1,000 in 2006; in 2007 and 2008, no
changes from 2006; 750 in 2010; 100–200 plants in October
2011; 407 stems in October 2011.
450 in 2000; 115 in 2002; 78 stems in 2003; 40 in 2004; between
20 and 40 in 2005; 50 in 2006; in 2007 and 2008, no changes
from 2006; 90 in 2010; 43 stem clusters in 2011.
200 in 2004; 75 plants in 2005; 10 in 2006; in 2007 and 2008, no
changes from 2006; 7 in 2010; 10 stem clusters in 2011.
200–250 in 2000 (also reported that 350 plants introduced); several
hundred blossoms in 2001; 70 in summer and fall of 2002; 182 in
2002; 291 stems in 2003; 100 in 2005; 350 in 2006; in 2007 and
2008, no changes from 2006, but only 150 seed pods in 2007;
120 in 2010; 101 stem clusters in 2011.
100+ in 1968; 50 in 1986; 50 in 1987; 13 in 1988; 7–9 in 1991; 2–3
in 1992; maximum of 27 in 1993; 38 in 1994; 41 in 1995; 16 in
1996 (only a partial survey); 15–20 on private land in 1997; 13 in
1998; 49 in 1999; 17 along ROW and 300 observed on private
land in 2000; 15 and 300+ on private land in 2001; 20 along
ROW and fewer than 100 observed on private land in 2002; 3 in
2003; 20 and 0 on private land in 2005; none in 2007; 35 along
powerline in 2010; 128 stem clusters along ROW in 2011.
1 in 1992 and 1993; 26 within 3 subpopulations in fall 1993; 1 in
1994–1996; 1 observed then an additional 75 in 1997 under
bridge; 1 in 1998; 2 in 1999; 16 in 2000; 5 in 2001; none in 2002;
17 in 2003; none in 2004, 2005, 2008, 2009; 46 in 2010 in 4 subpopulations; 1 plant in one subpopulation in summer 2011; 20
stem clusters in 6 subpopulations in 2011.
50 in 1991; 58 in 1993; 38 in 1994; 1 in 1995; 2 in 1996; 6 in 1997;
8–13 in 1998; 14 in 1999; 8 in 2000; 4 in 2001;12 in Sept. 2002;
none in Oct. 2002, 2003, 2004, 2005, or 2011. Considered
extripated.
50–70 in 1991; 7 in 1992; 58 in 1993; several hundred blossoms in
2001; 400 along ROW in 2002; 900 blossoms or seedpods in
2007; observed in 2008, but no estimates; 20 in 2010; 539 stem
clusters in 2011.
96 in 1995; hundreds in October 2011.
Herbarium specimen was recently confirmed again as H. dasycalyx,
but site has not been observed since 1980.
Hundreds in 1997; 300–400 in 2001.
No estimates. Searches occurred in 1992 and 1993, but no plants
were observed.
Populations along SH ROWs include
SH 94 in Trinity County, collected in
1955 (Blake 1958, p. 277); SH 204 in
Cherokee County, first observed in 1992;
and SH 230 in Houston County, first
observed in 1978. The TPWD performed
annual SH ROW monitoring along SH
94 from 1993 thru 2001 (Poole, 2001, p.
1); along SH 204 from 1993 thru 2003
(Poole 2001, p. 1; TXNDD 2012a, pp.
20–28); and along SH 230 from 1993
thru 2001 (Poole 2001, p. 1). These three
ROW populations are separated from
one another and are considered distinct.
However, the Boggy Slough site consists
of several scattered Neches River rosemallow subpopulations that are located
in close proximity to one another. Boggy
Slough subpopulations and the SH 94
ROW population are separated by no
more than 1.0 km (3,280 ft), and these
two sites likely constitute a single,
larger population, sharing pollinators
and exchanging genetic material
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(NatureServe 2004, p. 6; Poole 2011c, p.
2). Therefore, in Table 4, they are
combined and represented as a single
location.
Adjacent lands to the SH 230 ROW
were purchased by the Texas Land
Conservancy in 2004 (The Texas Land
Conservancy 2011), an organization
previously known as the Natural Areas
Preservation Association (NAPA). The
Neches River rose-mallow plants in this
site, referred to as Lovelady, are part of
a population that included the Neches
River rose-mallow plants in the SH 230
ROW. The Neches River rose-mallow
plants within the SH 230 ROW have not
been observed since 2002, and the site
is considered extirpated (TXNDD 2012a,
pp. 61–67). The Lovelady site was
recently surveyed in 2011, and although
539 stem clusters were found, most
were in notably poor condition, being
much shorter in stature because of the
drought and herbivory (Poole 2012b,
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pers. comm.; TXNDD 2012a, pp. 14–19).
The estimates of Neches River rosemallow displayed in Table 4 show wide
variations in plant numbers. Some of
this variation is due to incomplete
counts at the sites; in other words, only
a portion of the population was
counted. Meaningful trends cannot be
derived from these population
estimates.
Although annual monitoring of the
ROW sites was discontinued in the early
2000s, TPWD visited all of the ROW
sites in October 2011. In the past, along
SH 204 ROW, several subpopulations
existed along multiple portions of the
ROW; however, several of these
subpopulations were gone in 2011. The
recent drought conditions have allowed
surveyors to count Neches River rosemallow plants in parts of sites that were
not accessible in the past because the
sites were too wet. The increase in
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numbers of plants at some of the ROW
sites may be partially attributed to this.
The Davy Crockett NF, Houston
County, Texas, contains four extant
sites, three introduced and one natural,
of the Neches River rose-mallow. The
one natural population is found in
compartment 55 located west of the
Neches River. This site is considered the
most robust of all known extant
populations (Poole 2011c, p. 3) and is
almost entirely unaltered from its
originally observed state as a seasonally
wet flatwood pond, with vegetation
being distinctly zoned (TXNDD 2012a,
p. 29). The three introduced populations
are located in compartment 16, which
was introduced with 450 plants (Davis
2000, pers. comm.; McCormick 2002, p.
1; Service 2000, p. 3); compartment 20
with 200–250 plants (Davis 2000, pers.
comm.; McCormick 2002, p. 2; Service
2000, p. 3); and compartment 11 with
about 200 plants (Nemec 2005, pers.
comm.). The populations in
compartments 16 and 20 were
introduced in 2000, while the
population in compartment 11 was
introduced in 2004 (Service 2007, p. 6).
All four of the Davy Crockett NF sites
were censused in October 2011, by the
Service and TPWD, and all of the
introduced sites on the Davy Crockett
NF appear to have declined
dramatically.
The four remaining Neches River
rose-mallow sites have had sporadic
monitoring or have not been visited in
recent years. In 1995, Stephen F. Austin
State University Mast Arboretum
planted 96 Neches River rose-mallow
plants into a site at Mill Creek Gardens,
Nacogdoches County (Scott 1997, pp.
6–7). A conservation easement was
placed on this land, and now the site is
managed by the Mast Arboretum.
Neches River rose-mallow plants at this
site were observed in 1997, 1998, 2001,
2009, and 2011 (Creech 2011a, pers.
comm.). The introduced plants appear
to be doing well; however, nonnatives
and native species are becoming more
prevalent, and may compete with the
Neches River rose-mallow (Creech
2011c, pers. comm.). Another site in
Harrison County, Texas, was last
verified by a specimen collected in
1980. The identification of this
specimen was identified as Neches
River rose-mallow and later considered
Hibiscus laevis (Melinchuk 2012, p. 2).
Not until 2011, was it confirmed that
the specimen collected was the Neches
River rose-mallow (Birnbaum 2011,
pers. comm.; TXNDD 2012a, pp. 12–13).
Although, the Harrison County site has
not been visited since 1980, and drought
and severe storms might have impacted
this site but without a lack of evidence
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suggesting the species’ extirpation from
either threat, we presume that Neches
River rose-mallow is extant at this site.
Two additional populations occur on
private lands in Trinity County: the
Camp Olympia and Champion sites,
discovered in 1977 and 1996,
respectively. The current status of
Neches River rose-mallow on the Camp
Olympia site is unknown. We consider
this site to be extant because we have no
evidence that it has been extirpated. The
population on the Champion site was
observed in 2001; plants were seen, but
no plant counts were done.
Conservation
We relied on Pavlik’s Minimum
Viable Population analysis tool (1996,
pp. 127–155) and species’ experts to
determine the conservation goals of the
species. Based on the best known and
available scientific information on the
species’ life-history and reproductive
characteristics, we concluded that the
conservation goals for the Neches River
rose-mallow include 10 viable
populations, each containing at least
1,400 individual plants. The species is
limited to the Neches, Sabine, and
Angelina River basins and the Mud and
Tantabogue Creek basins with 11 extant
sites throughout this range. However,
many of these sites were introduced and
are now compromised by threats from
feral hog damage, hydrological changes,
nonnative and native species
encroachment into habitat, construction
projects, and herbicide overspray.
Future management actions that
ameliorate these threats could allow for
the species to expand within its known
range. The extant populations are
generally small. The only site that has
come close to reaching the conservation
goals is on compartment 55 of the U.S.
Forest Service (USFS); however, it still
only comprises 53 percent of the needed
plants at this site (750 plants were seen
in 2010).
Summary of Comments and
Recommendations
We requested written comments from
the public on the proposed listing for
the Texas golden gladecress and Neches
River rose-mallow during two comment
periods. The first comment period,
associated with the publication of the
proposed rule (77 FR 55968), opened on
September 11, 2012, and closed on
November 13, 2012. Newspaper notices
inviting general public comment were
published in the Houston County
Courier, Nacogdoches Daily Sentinel,
and Marshall News Messenger. We also
requested comments on the proposed
listing during a comment period that
opened April 16, 2013, and closed on
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May 16, 2013 (78 FR 22506). We
received requests for a public hearing,
which was held on May 1, 2013, in
Nacogdoches, Texas. Newspaper notices
inviting public comment for this second
comment period were published in the
San Augustine Tribune and Cherokeean
Herald in addition to the three papers
listed above. We also contacted
appropriate Federal, State, and local
agencies; scientific experts and
organizations; and other interested
parties and invited them to comment on
the proposed rule during these comment
periods.
We received approximately 63 public
comments. All substantive information
provided during both comment periods
has either been incorporated directly
into this final determination or is
addressed below. Comments addressed
below are grouped into general issues
specifically relating to the listing of
Texas golden gladecress and Neches
River rose-mallow.
Peer Review
In accordance with our peer review
policy published on July 1, 1994 (59 FR
34270), we solicited expert opinions
from six knowledgeable individuals
with scientific expertise that included
familiarity with the biology and ecology
of the Texas golden gladecress and
Neches River rose-mallow; the
geographic region in which these
species occur and characteristics of their
habitats, including the unique geology;
and land uses common to the region
that may bear on the threats to both
species. We received responses from
four of the peer reviewers.
We reviewed all comments we
received from the peer reviewers for
substantive issues and new information
regarding listing of the Texas golden
gladecress and Neches River rosemallow. The peer reviewers generally
agreed with portions of our assessment,
including the threats analysis, and most
of our conclusions, although they
pointed out areas where additional
research would refine our
understanding of the two species’
habitat requirements and range. The
peer reviewers provided additional
information, clarifications, and
suggestions for future research that
would inform future surveys to refine
the geographic range and that would
help with management and recovery
efforts. Peer reviewer comments are
addressed in the following summary
and incorporated into the final rule as
appropriate.
Peer Reviewer Comments
(1) Comment: One peer reviewer
asked for clarification regarding the
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numbers of Texas golden gladecress
populations in State highway ROWs.
One location in the proposed rule
referred three extant sites within State
highway ROW; however, another
location refers to only two extant
populations within State ROWs.
Our Response: We recognize that the
language in the proposed rule may be
misleading or easily misconstrued
because it implies that the three
confirmed Texas golden gladecress
populations are all located in ROWs. We
have changed the language in the
referenced paragraph to reflect the fact
that only two of the extant populations,
Geneva and Caney Creek Glade Site 1,
occur in ROWs, which are both
managed by TXDOT. The third extant
population at Chapel Hill is located on
a small tract adjacent to a county road
and is not considered to extend into any
type of road ROW.
(2) Comment: One peer reviewer
stated his opinion that that there is no
conservation land, fee simple or under
easement, for either of these species. He
alluded to the land on which these
species’ habitats occur being some of the
cheapest in east Texas and suggested
that it would be more cost effective to
purchase fee title or conservation
easements of small tracts to conserve
these species because creation of a
series of small protected sites would
work well for an endemic species. He
indicated that the habitat areas in
question have very little commercial
value, with the Weches glades having
no value for forestry or agriculture. He
acknowledged that the value of the
Weches Formation for glauconite
mining exceeds values for other uses
and indicated his opinion that it would
be appropriate to estimate the
commercial value of the glauconite
mined on a site and match this value.
Our Response: We are in agreement
with the first part of this comment about
the lack of conservation lands for the
Texas golden gladecress; however, this
is not true for the Neches River rosemallow. The Texas Land Conservancy
has fee title ownership of the land on
which the Neches River rose-mallow’s
Lovelady population in Houston County
is located. The Texas Land Conservancy
bought this land specifically to conserve
the Neches River rose-mallow and
manages the site accordingly. The
United States Forest Service (USFS) also
has Neches River rose-mallow in several
compartments, is aware of the species,
and manages those compartments to
avoid impacts.
Further, the Act requires us to
determine if the Texas golden gladecress
and Neches River rose-mallow warrant
listing solely on the basis of the best
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scientific and commercial data available
as evaluated through our assessment of
the five listing factors set forth in the
Act. We previously determined that the
Texas golden gladecress and Neches
River rose-mallow warranted listing
under the Act, making them candidate
species. However, the listing of these
species was precluded by the necessity
to commit limited funds and staff to
complete higher priority listing actions
for other species. The Texas golden
gladecress and Neches River rosemallow have been included in our
annual candidate notices of review for
multiple years. In our annual review of
these species, scientific literature and
data have, and continue to, indicate that
these species are impacted by ongoing
threats. Any future conservation actions,
such as purchasing land from willing
landowners, or land management efforts
to ameliorate threats, will be evaluated
as part of the recovery planning process.
(3) Comment: Two peer reviewers
discussed the geography of the Weches
Formation and wondered how it may
influence the range of the Texas golden
gladecress. One reviewer indicated that
it is a common misconception that the
Weches Formation centers on
Nacogdoches and San Augustine
Counties. He pointed out that the
Weches Formation also extends over
100 miles (161 km) to the north into
Smith, Wood, Upshur, Marion, and Cass
Counties in Texas, and even across into
Miller County, Arkansas. A second
reviewer described the Weches
formation as consisting of Eocene age
deposits lying mostly in an east-west
band. This reviewer further pointed out
a northeast to southwest trend in
Cherokee County, Texas, proceeding
northeastward toward Tyler, Texas.
Referencing the U.S. Department of
Agriculture’s soils surveys of Cherokee,
Nacogdoches, Houston, San Augustine,
and Sabine Counties, the reviewer
indicated that most acreage of Weches
Outcrop may occur in Cherokee County.
The former reviewer indicated that he
was not aware of any systematic surveys
of these widely dispersed outcrops for
the presence of the endemic glade
plants. He recommended that some
attention and resources be directed at
exploring the other Weches outcrops
that stretch north to Cass County and
suggested that any ruling by the Service
or subsequent recovery plan for Texas
golden gladecress include provisions for
surveying these areas.
Our Response: The Service recognizes
the extent of the Weches Formation
reaches the above referenced counties.
However, the Service has not found or
received any data indicating that the
species is present in these other
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56035
counties. The Service is required to use
the best scientific and commercial data
available at the time of listing. We relied
on all available information regarding
the known occurrences of the Texas
golden gladecress at the time of listing;
none of the known occurrences was
reported from outside Sabine and San
Augustine Counties (with the exception
of the introduced population in
Nacogdoches County). Further analysis
of geological correlations with the Texas
golden gladecress is an issue to be
addressed in recovery planning.
Furthermore, as a federally listed
endangered species, the Texas golden
gladecress will be afforded the
protections of the Act wherever found.
(4) Comment: One peer reviewer
pointed out that our assessment of the
Weches Formation did not take into
account the work of geologists. He
suggested referencing the body of work
on the chemistry and mineralogy of the
Weches by Ernest Ledger and students
that document a wide variation in the
attributes of the Weches across its range
from San Augustine and Nacogdoches
Counties, north over 100 miles (161 km)
to Cass County. In his opinion, we need
to know about the variability of the
Weches Formation in terms of available
calcium and long-term pH change to
identify more potential sites for the
Texas golden gladecress. This reviewer
indicated that Ledger’s chemical
analyses of Weches constituent minerals
shows hard data on the low-level
presence of nutrients in some locations.
Some of these may be suitable for
mining as soil additives in the future
when current sources like phosphate
rock deposits are mined-out. Analyses
of the chemical composition of the rock
should be considered when selecting
potential conservation sites. He
suggested that a critical look at Ledger’s
work might show that unusual features
of the Weches Formation that promote
the occurrence of Texas golden
gladecress and associated glade plants
are limited to the southern end of the
Weches Formation. Similarly, this peer
reviewer referred to the known
variations in the Weches Formation and
suggests that we need a better
understanding of the geology and soils
conditions underlying Texas golden
gladecress in order to plan for future
surveys for the species.
Our Response: We recognize that
variability of Weches outcrops does
exist across the Weches Formation
throughout the numerous counties
listed above. We agree that a better
characterization of the geology and soils
underlying known Texas golden
gladecress populations could provide
useful information. However, there are
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likely other factors that characterize
individual outcrop sites that may also
be important (for additional
information, see ‘‘Invasive Species’’
under A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range of
this rule). Further, the Service must use
the best available scientific and
commercial data available at the time of
listing. Determining the chemical
components of the geological formations
beneath known glade sites is not a
feasible accomplishment within the
timeframe we have to publish our final
determination. This research would be
addressed in recovery planning. For
purposes of the proposed rule and this
final rule to list the Texas golden
gladecress, we used the more general
Weches Formation outcrops
descriptions, and we more specifically
relied on the geologic and soils
information available from one known
Texas golden gladecress population site,
as well as from one white bladderpod
site. Please see the ‘‘Habitat’’ section for
the Texas golden gladecress in this final
rule for more information.
The commenter did not provide
specific references for Ledger’s research.
However, we attempted to locate
research conducted by Ledger on this
topic. We were able to locate some of
Ledger’s research, and we incorporated
this into this final rule under the
‘‘Habitat’’ section for the Texas golden
gladecress. However, this information
did not modify our conclusions of our
analysis of threats or determination that
the species meets the definition of an
endangered species under the Act.
(5) Comment: One peer reviewer
commented that the essential habitat
component of Weches outcrops
underlying Texas golden gladecress
populations is the combination of thin
soil over a calcium-rich parent material.
In the Weches Formation, the calcium is
derived from a myriad of fossilized,
calcium-dominated oyster shells and
other marine life.
Our Response: The peer reviewer’s
verbiage was added to the Texas golden
gladecress’s ‘‘Habitat’’ description in
this final rule to further illustrate the
derivation of calcium from marine
organisms that is true of the east Texas
Weches Formation and which may be
different from habitat of other
Leavenworthia species.
(6) Comment: One peer reviewer
indicated that the developed soils that
occur near the Weches outcrops are
included in the Bub, Trawick,
Nacogdoches, or Chireno soil series. He
described the Chireno soil series as
unique because it is the only ‘‘blackland
soil’’ in east Texas. Chireno soils are
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classified as ‘‘mollisols’’ or blackland
soils and are developed under
prolonged grassland habitat. This
reviewer used the U.S. Department of
Agriculture’s soil surveys for Sabine,
San Augustine, Nacogdoches, and
Houston Counties to estimate roughly
3,000 acres (1,214 ha) of this soil type
occurring in a four-county area. He
indicated that these soils may underlie
prairies (glades) and that Native
Americans regularly burned these areas
either for protection from wildfires or
enemies, or to entice game animals.
Our Response: Although the reviewer
does not specifically suggest that we
add Chireno soils to the other soils
known to support Texas golden
gladecress habitat, this is how we have
interpreted his comment. Based on the
development of these blackland soils
being dependent on long-term prairie
cover, and the fact that other literature
describes the Pineywoods glades as
being within prairies, or as part of a
combination of prairies and glades,
information may indicate the potential
for Weches outcrops within this soil
series to support the herbaceous glades
of which Texas golden gladecress may
be a component. Mollisols, of which the
Chireno series is one, are soils of
grassland ecosystems, characterized by a
thick, dark surface horizon that was
developed under prolonged grassland
habitat (Grunwald 2013, pp. 1–2). We
based the soil parameters for Texas
golden gladecress habitat on the soil
descriptions in the TXNDD’s element of
occurrence records, the thesis by Robert
George (George 1987, entire), and the
U.S. Department of Agriculture’s soil
survey layers underlying all known
Texas golden gladecress populations.
The known Texas golden gladecress
occurrences are all found on shallow,
gravelly soils or almost bare bedrock
overlying Trawick, Bub, or Nacogdoches
soils, situations that would not support
dense stands of prairie grasses, at least
in the portion of the outcrop where the
Texas golden gladecress is growing.
Further investigation of the Chireno
series for the presence of Texas golden
gladecress would be addressed during
the recovery process.
(7) Comment: One peer reviewer
provided us with confirmation that the
glade habitat at the Texas golden
gladecress population site referred to as
Caney Creek Glade 7 was still intact as
of spring 1996, when this reviewer
visited the site. However, on a second
visit in 2000, encroachment by weedy
and woody species was prevalent at this
site.
Our Response: This comment affirms
our 2012 evaluation of this site, as
derived from analysis of satellite
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imagery. As indicated in our proposed
rule and this final rule, the population
being referenced may still be present as
of 2012, but from satellite imagery the
site appeared to be overgrown with
woody vegetation. Based on the habitat
at Caney Creek Glade Site 7 remaining
intact (not excavated or built over), with
the exception of woody overgrowth, we
assume that Texas golden gladecress
plants still occupy this site.
(8) Comment: One peer reviewer
relayed personal observations that
accumulation of pine leaf litter and
eventual degradation of the material
supports the germination of pine seed.
This reviewer indicated that this likely
happens because the leaf litter debris
provides a small but steady increase of
soil depth on the rocky, thin soil
common in the Weches glades.
Our Response: This comment
supports the data in our proposed rule
and this final rule to list the Texas
golden gladecress, which state that
planting of pine trees in close proximity
to small glades may produce leaf litter
that can accumulate within a glade,
sometimes covering its surface and
smothering smaller glade plants. As
noted by the reviewer, the accumulation
of pine leaf litter and the byproducts of
its decomposition would create and
enhance layers of organic material and
create conditions favorable to natural
pine seedling establishment. This would
alter the nature of the glades by
eventually deepening soils within the
glade, thereby allowing other plants,
including woody plants that previously
did not occur in the short, herbaceous
plant community, to take over these
areas that formerly had too shallow and
poor soil to support shrubs and trees.
This situation would also enhance
invasion by other plants, including
Macartney rose, that would benefit from
additional soil. Not only would the
glade vegetation undergo succession to
shrubs and trees, but the glades would
also be altered by the shading and
would hold moisture in the soil. All of
these conditions would impede the
continued existence of the Texas golden
gladecress by altering the competitive
advantage that this plant has in the
glade environment.
(9) Comment: One peer reviewer
suggested evaluating a specific,
potential Texas golden gladecress site
based on the presence of the Texas
golden gladecress’s known associated
species. The site is located on the SH 21
ROW, near the Sabine, Davy Crockett
NF compartment 76, adjacent to a
glauconite quarry.
Our Response: From information
provided to us early in the proposed
rule’s preparation stage, we were aware
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that flora and fauna surveys were done
on USFS lands in Sabine County in
association with the debris cleanup
effort post-Hurricanes Rita and Ike.
These surveys, in conjunction with
results of botanical surveys conducted
before this time, failed to document the
Texas golden gladecress on any of these
USFS lands, although we do not know
if lands outside of the USFS were
included in any of the surveys.
However, strategies for continued
evaluation of potential but unconfirmed
new sites will be addressed during the
recovery planning process.
(10) Comment: One peer reviewer
suggested that mention be made of the
possibility for illuminating the
evolutionary history of these species by
genetic studies and that this would be
useful in determining management
strategies.
Our Response: This is an issue that
may be addressed during recovery
planning.
(11) Comment: A peer reviewer
provided additional literature to
consider in our analysis on the
hybridization of the Neches River rosemallow. One was by Klips (1995) and
the other by Mendoza (2004). These
studies provide genetic insight of the
relatedness between Neches River rosemallow and two co-occurring species,
Hibiscus moscheutos and H. laevis. Both
researchers agree with the Service’s
opinion that the Neches River rosemallow is a distinct species. These
studies review the relatedness between
the Neches River rose-mallow and other
species; however, they do not
investigate hybridization. Another peer
reviewer noted the potential
hybridization of the Neches River rosemallow on compartment 20 in the Davy
Crockett NF, in October 2012. Plants
appeared to be H. dasycalyx, but the
calyx was lacking the hairy surface
typical of the species. The reviewer
thought that the species was a potential
cross with H. laevis.
Our Response: The Service has
reviewed this new information and
incorporated it into the threats section
under ‘‘Hybridization’’ in this final rule.
These studies pertain to the relatedness
between the Neches River rose-mallow
and other species. They do not
investigate hybridization of these
species. Although the genus Hibiscus
readily hybridizes within the nursery
trade, hybridization between Neches
River rose-mallow and another Hibiscus
under natural conditions has not been
verified. Drought conditions can alter
the plants morphological or physical
characteristics including leaf size,
structure, and overall plant height (Fair
2009, p. 1). Further investigation into
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the occurrence of hybridization and its
impacts on the population are
necessary. The University of Texas–
Tyler is researching the hybridization
issue for Neches River rose-mallow and
its impacts on the population; however,
the project is only in its infancy, and no
results have been determined. We do
not consider hybridization a threat to
the Neches River rose-mallow at this
time.
(12) Comment: One peer reviewer
reported that in October 2012, she and
a USFS botanist observed sedimentation
along ROW work on both sides of SH
94. They anticipated that resurfacing
and re-crowning work of the highway
will likely increase runoff to this site.
The reviewer noted that, during road
improvement, TXDOT installs
temporary culverts to assure water flow
and exchange during construction.
Another reviewer questioned whether
county and municipal governments,
who buy glauconite for road projects,
are required to demonstrate that
endangered species like white
bladderpod are not being negatively
impacted by their road-building
activities. He further asked whether the
counties are receiving State or Federal
funds to assist with road building.
Our Response: The Service is aware of
the bridge replacement along SH 94, but
as of 2011, the construction and
associated impacts of this project had
not progressed into Neches River rosemallow habitats (Adams 2011c, pers.
comm.). Since the start of the SH 94
road expansion project, TXDOT has
employed the use of temporary culverts
and orange construction fencing around
Neches River rose-mallow sites and has
restricted workers from these fenced-off
areas. Fenced-off areas encompassed far
more area than that habitat known to be
occupied by the Neches River rosemallow (Adams 2013b, pers. comm.). In
wetlands where sedimentation might
continue despite the use of the above
management activities, silt curtains (or
silt fence) placed in conjunction with
orange construction fencing have been
installed (Adams 2013b, pers. comm.).
Currently, all avoidance measures are
voluntary.
However, on the effective date of this
final rule (see DATES), the Neches River
rose-mallow will become a federally
threatened species under the Act.
Section 7(a)(2) of the Act requires
Federal agencies to ensure that activities
they authorize, fund, or carry out (that
is, projects with a Federal nexus) are not
likely to jeopardize the continued
existence of the species or destroy or
adversely modify its critical habitat, if
any is designated. If a Federal action
may affect a listed species or its
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56037
designated critical habitat, the
responsible Federal agency must enter
into consultation with the Service (see
Available Conservation Measures in this
final rule for more discussion of this
process). If this project, or any other
project, has a Federal nexus and the
project may affect a federally listed
species then the Federal action agency
will need to consult with the Service.
We are publishing a final rule on the
designation of critical habitat the Texas
golden gladecress and the Neches River
rose-mallow under the Act elsewhere in
today’s Federal Register.
(13) Comment: One peer reviewer
made several comments on invasive
species and provided the Service with
new information on the biology of
Chinese tallow. The reviewer’s recent
observations in 2012, along with a USFS
botanist, found Chinese tallow and
Melia azedarach (Chinaberry) within
compartment 16, Davy Crockett NF.
Chinese tallow has invaded all known
Neches River rose-mallow sites, yet is
more prominent in SH 94 and
compartment 16, Davy Crockett NF
sites. The reviewer provided a literature
citation, Gan et al. 2009. Additionally,
the reviewer mentioned that coastal
bermudagrass (Cynodon dactylon) is one
of the most serious, nonnative, invasive
species threats to the Neches River rosemallow.
Our Response: As described in the
proposed rule, we agree with the peer
reviewer that nonnative species are a
threat to the Neches River rose-mallow.
We incorporated the additional
information and biological data on
tallow provided in Gan et al. 2009 into
the Summary of Factors Affecting the
Species section of this final rule. This
additional information did not modify
our listing determination.
At the time the proposed rule was
published, we were only aware of one
location at Boggy Slough in Houston
County where coastal bermudagrass was
observed. However, new information
was provided to the Service during a
public comment period. We are now
aware of three additional sites where
encroachment from coastal
bermudagrass was observed. These sites
included: The Texas Land Conservancy,
where it is common; SH 204 ROW,
where it is abundant (Poole 2013a, pers.
comm.); and the original site at the SH
94—Boggy Slough, where it is locally
common in the interior of the unit
(Allen 2011a, pers. comm.). At the
planted site on Boggy Slough, Neches
River rose-mallow was observed as
recently as August 2012. Although the
coastal bermudagrass has the potential
to spread and grow quickly, and has
been known to form monocultures along
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highway ROWs, the Neches River rosemallow and coastal bermudagrass do
not necessarily grow naturally in the
same habitat. Coastal bermudagrass is
not typically found within wetland
areas. Further, the Neches River rosemallow is a taller growing species, a
feature that prevents itself from being
shaded out by coastal bermudagrass.
Based on the above information, the
Service does not consider coastal
bermudagrass a threat at this time. The
TPWD concurs with the Service that
coastal bermudagrass is not considered
a threat at this time (Poole 2013a, pers.
comm.).
The nonnative species Chinaberry has
not been previously noted at any of the
sites, including the site mentioned by
the commenter, compartment 16 on the
Davy Crockett NF. The Service
investigated this comment further, and
Chinaberry was not mentioned in the
TXNDD database information. Based on
this information the Service does not
consider Chinaberry a threat at this
time.
(14) Comment: A peer reviewer
indicated that due to drought in 2011,
the numbers of plants were a lot fewer
than years previous in SH 94 ROW and
compartment 55, Davy Crockett NF. On
October 3, 2012, observers went to
specific locations in these
compartments where plants were
known to occur, and none could be
found. In 2013, rainfall has been about
average to date, but the reviewer
concluded that effects were evident
from previous drought.
Our Response: We agree that drought
has caused impacts to said populations
and likely other populations. Drought
conditions have reduced the number of
plants and have stunted overall Neches
River rose-mallow plant growth
(TXNDD 2012a, p. 8). We do not have
knowledge of how drought affects the
Neches River rose-mallow on a larger
scale or how it impacts flowering or
seed production. However, it is possible
that during drought conditions, floral
characteristics that are normally easily
recognizable could be reduced and
make identification of Neches River
rose-mallow more difficult (Poole
2012b, pers. comm.). Since the Neches
River rose-mallow is a wetland species,
we understand that drought conditions
could continue to threaten the habitat as
well as the reproductive capability since
it is likely that seed dispersal is watermediated. With the likelihood that
seasonal or successive year-round
drought conditions will likely continue,
ancillary threats from trampling and
herbivory may be exacerbated. Drought
is discussed in the Summary of Factors
Affecting the Species in this final rule.
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(15) Comment: One peer reviewer
noted that in spite of the fact that Sabine
and San Augustine Counties have not
seen major increases in human
population, there has been improvement
of services, such as communication
lines, water lines, domestic gas lines,
and power lines. These actions occur
primarily in ROWs, and some occur in
areas that are situated in potential Texas
golden gladecress habitat.
Our Response: We acknowledge that
the installation of new service lines
(e.g., communication, water, domestic
gas, and power lines) could potentially
occur in more rural areas, and these
activities typically occur in road ROWs,
such as where the Texas golden
gladecress occurs. There are two known
Texas golden gladecress sites that
extend into road ROWs. When this rule
is effective (see DATES), section 7
consultation requirements and section 9
prohibitions under the Act will apply to
the Texas golden gladecress and Neches
River rose-mallow. See our response to
Comment 12 and Available
Conservation Measures for more
discussion of this process.
(16) Comment: One peer reviewer
pointed out an example of the flaws of
teaming these two species together can
be seen in the statement in the proposed
rule that says, ‘‘Prolonged or frequent
droughts can exacerbate habitat
degradation for both species.’’ He
indicated that a river-bottom dwelling
species like the Neches River rosemallow might be negatively impacted
when drought allows other species to
encroach. However, drought could
positively impact Texas golden
gladecress as it might exclude woody
closure of glades. This reviewer noted
his personal observation of the drought
of 2011 dramatically pushing back the
edges of glades in the Weches and in
tiny saline prairies.
Our Response: We agree that the
droughty conditions of hot, dry
summers are a part of the reason why
Texas golden gladecress can remain
competitive on the glades. However,
prolonged drought, especially when it
occurs in successive years, has resulted
in Texas golden gladecress not
appearing above ground in some years,
and therefore not flowering or
producing seed in those years. We do
not know how many years of poor seed
production, or no seed production at all,
will affect the survival of the
population. Negative impacts of drought
on the Neches River rose-mallow are
discussed in our response to Comment
14 as well in the Summary of Factors
Affecting the Species section of this
final rule.
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(17) Comment: A peer reviewer
commented on the occurrence and use
of nonnative and potentially invasive
pasture grasses such as coastal
bermudagrass, Paspalum notatum
(bahiagrass), and Lolium perenne
(perennial ryegrass), which are
commonly used to re-vegetate many
road ROWs. These grasses are common
on most ROWs and aggressively grow in
open, sunlit areas.
Our Response: The Service recognizes
the occurrence and use of nonnative and
potentially invasive pasture grasses
along ROWs, and that ROWs typically
become monoculture stands of these
invasive species, thereby out-competing
natives. The Service has verified that
both coastal bermudagrass and
bahiagrass are included in mixtures
used to re-seed ROWs (Adams 2013c,
pers. comm.). There are two Texas
golden gladecress and three Neches
River rose-mallow known populations
growing along ROWs, which could be
planted with nonnatives. We are not
aware of any Texas golden gladecress
sites where the Texas golden gladecress
itself is being impacted by these grasses.
Coastal bermudagrass has been observed
on four Neches River rose-mallow sites
(see our response to Comment 13 for
additional details). We investigated
these nonnative species as potential
threats and incorporated this
information into our analysis in the
Summary of Factors Affecting the
Species section for the Texas golden
gladecress and Neches River rosemallow in this final rule. There is the
potential for such nonnative, invasive
species to impact the Neches River rosemallow, as well as the Texas golden
gladecress, in the future if these grasses
out-compete native plants for soil
nutrients, space, and light. However,
these invasive species are not currently
a threat, and there are no data indicating
that these species will be a threat in the
near future.
(18) Comment: One peer reviewer
provided new observations about
damage to habitat due to feral hog
activity. In October 2012, feral hogs had
broken and flattened plants in
compartment 16, Davy Crockett NF.
Large groups of feral hogs were seen in
two Neches River rose-mallow sites
(compartment 55 and compartment 16,
both in the Davy Crockett NF). Neches
River rose-mallow habitat is only
surficially dry and can be easily
disturbed by hogs, as made evident in
compartment 20, Davy Crockett NF.
Our Response: The Service has
included this information in our
analysis of feral hog impacts on the
Neches River rose-mallow in the
Summary of Factors Affecting the
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Species section in this final rule. Based
on this information, the Service
recognizes that feral hogs impact the
species and that feral hogs will likely
continue to impact the species in the
near future. However, at this time, the
severity of impacts to the species is low.
The level of impacts from feral hogs
does not change the determination to
list the species as threatened versus
endangered.
(19) Comment: One peer reviewer
commented on the impacts that beavers
have had on one Neches River rosemallow site: Compartment 16, Davy
Crockett NF. In general, water levels
fluctuated due to beaver activity. It was
observed that larger trees along the
water’s edge were damaged by beavers,
although it appears that water levels had
receded to the same level prior to the
beaver activity.
Our Response: The Service is aware of
beaver presence at compartment 16 of
the Davy Crockett NF. We acknowledge
that beaver activity (i.e., dams) could
have impacted this Neches River rosemallow site. However, with seasonally
fluctuating water levels and no
estimates on plant abundance before
and after beaver activity, it is unclear
how or if beaver activity was a factor in
the size of the Neches River rose-mallow
population. We are uncertain if there
was a correlation between the damage
done to this site and the changes in
water flow and the site hydrology, and
whether this had a positive or negative
impact on the species. No other sites
have been impacted by beaver activity.
We do not consider the effects of beaver
damming to be a threat to the Neches
River rose-mallow.
(20) Comment: One peer reviewer
agreed with the use of Weches
glauconite as road base material being a
threat. He indicated his belief that it
should be possible to locate Weches
mines where conditions are not suitable
for the glade community and reiterated
that the Weches is a highly variable rock
formation. This peer reviewer provided
new information about other uses for
Weches glauconite, including animal
feed additives, that were not addressed
in the proposed rule. This reviewer
expressed his opinion that it is also
possible that in a few decades the
shortage of mineral phosphate rock
might make some of the deposits viable
for agriculture use. He referred to
information from Dr. Ernest Ledger
(geologist) regarding instances where
rare earth elements are being mined in
the Weches or Reklaw Formations.
Our Response: In analyzing threats to
a species, the Service uses the best
scientific and commercial data available
to analyze the current threats and
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threats anticipated to occur in the near
future. The Service has identified
quarrying Weches glauconite as a
current and future threat to the Texas
golden gladecress. We know that several
Texas golden gladecress populations
have been lost in areas where glauconite
quarries were developed (see the
Summary of Factors Affecting the
Species sections of the proposed rule
and this final rule). We did not
specifically identify animal feed
additive as a use for the Weches
glauconite in our proposed rule, but we
have incorporated this information into
the Summary of Factors Affecting the
Species section of this final rule. The
impact to the species from quarrying is
the clearing and excavation of
vegetation and soil during development.
The specific uses of the Weches
glauconite are not relevant to the
impacts from quarrying. However, new
uses or an increase in current uses of
Weches glauconite may increase the
demand of this resource and therefore
increase the amount of quarrying
activities (that is, ground disturbance).
However, the Service does not have
information that either of these are
occurring.
Section 7 of the Act requires Federal
action agencies to consult with the
Service to ensure their action do not
jeopardize the continued existence of
the species. However, there are limited
or no Federal nexuses for glauconite
quarry projects. Entities implementing
projects that could impact the Texas
golden gladecress could play a
significant role in the conservation of
the species by voluntarily working with
the Service, the State, or conservation
groups to construct their projects in
such a way as to avoid or minimize
impacts to the species. Site selection of
quarries outside of endemic plant
communities containing Texas golden
gladecress could be a measure to avoid
or minimize impacts to the species.
Additional research of the habitat
requirements of the Texas golden
gladecress, particularly the surface soils
and subsurface composition of the
bedrock, may help in determining
whether there are particular outcrops
that should be protected for Texas
golden gladecress versus ones that will
never support the species and would
therefore not be problematic if selected
for a quarry. This is an issue that may
be addressed during recovery planning.
(21) Comment: One peer reviewer
suggested using genetic evidence to
evaluate how past climate changes,
particularly drought, as well as
dispersal mechanisms and barriers to
dispersal, may have affected the
distribution and endemism of the Texas
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56039
golden gladecress and the Neches River
rose-mallow. He indicated his opinion
that a better understanding of these
factors would have bearing on future
management considerations.
Our Response: It is possible that the
past droughts have affected the
distribution of Neches River rosemallow and Texas golden gladecress in
east Texas. For Neches River rosemallow, geographic barriers may have
arisen due to past drought events,
potentially limiting genetic exchange
between populations. Humans may have
contributed to further endemism of the
species by altering habitat, which
functionally created barriers to dispersal
and resulted in more isolation of
populations. However, we can only
postulate that these are the reasons for
the endemism of the Neches River rosemallow to certain river systems, and
more specifically to surficially dry
habitats as compared to other east Texas
Hibiscus species. Additional research is
needed to assess the validity of this
hypothesis.
With regard to the Texas golden
gladecress, the Weches outcrops
generally occur in small, isolated or
segmented strips (George 1987, p. 4;
George and Nixon 1990, p. 118), making
the habitat, in essence, small islands
separated from one another by
dissimilar habitat. The current
patchiness and separation of the Texas
golden gladecress population sites may
be, at least in part, due to past droughts,
but may also be a result of the habitat
being fragmented by land conversions or
lost to succession by woody species.
Because we lack information on seed
dispersal of Texas golden gladecress, we
do not know how the species spread
historically or how it came to be
distributed where it is. Therefore, we do
not know if the isolation of the
populations is due to vicariance
(populations on outcrops that are
geographically separated by
surrounding forest) or due to a lack of
dispersal to new habitats or between
population sites. Genetic evidence may
help to clarify the relatedness or lack
thereof between the remaining extant
populations, but that may be undertaken
as part of the recovery process.
(22) Comment: One peer reviewer
commented that the presence of a
currently listed endangered species,
white bladderpod, confers some
protection for other Weches glade plants
at sites where it occurs.
Our Response: There are two Texas
golden gladecress sites where white
bladderpod is also found: Chapel Hill
and Caney Creek Glade Site 1.
Additionally, both species were known
to co-occur at historical Caney Creek
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Glade Site 6, but they were eliminated
by construction of a quarry. The entirety
of the Chapel Hill site is privately
owned, with all Texas golden gladecress
plants growing strictly on private land.
This situation is also true for most of the
Texas golden gladecress plants at the
Caney Creek Glade Site 1, although a
limited number of individuals extend
into the adjacent TXDOT-managed
ROW. Although there are not formal
legal protections for listed plants on
private land, if a project takes place on
that privately owned property that is
carried out, permitted, or funded by a
Federal agency, a Federal nexus is
established for that project, and that
Federal action agency is responsible for
section 7 consultation with the Service
to avoid jeopardizing the species or
adversely modifying any designated
critical habitat. For the plants in the
ROW at Caney Creek Glade Site 1,
TXDOT will provide protections for the
species per State regulations or through
consultation with the Service.
Comments From States
Section 4(i) of the Act states, ‘‘the
Secretary shall submit to the State
agency a written justification for his
failure to adopt regulations consistent
with the agency’s comments or
petition.’’ Comments received from the
State agencies and government officials
regarding the proposal to list the Texas
golden gladecress and Neches River
rose-mallow are addressed below.
(23) Comment: These species have not
been fully studied. There are significant
concerns with the quality of data and
analysis the Service used for its
determination. The proposal is based
largely on inconclusive reports and vast
speculation about operations thought to
affect habitats, existing regulatory
mechanisms, conservation efforts,
species populations and potential
threats that fail to provide any sound
scientific foundation on which to justify
the listing of these species.
Our Response: It is often the case that
biological information may be lacking
for rare species; however, the Act
requires the Service to make
determinations based on the best
scientific and commercial data available
after conducting a review of the status
of the species and after taking into
account those efforts, if any, being made
to protect such species. We are also
required to make our listing
determinations based on the five threat
factors, singly or in combination, as set
forth in section 4(a)(1) of the Act.
We sought comments from
independent peer reviewers to ensure
that our designation is based on
scientifically sound data, assumptions,
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and analysis. Peer reviewers were
generally in agreement with the
conclusions from our threats analysis
that habitat modification and
destruction due to human activities, as
well as woody encroachment into
Weches glades, likely adversely affects
the Texas golden gladecress. The
reviewers enhanced our understanding
of some threats by providing personal
observations of habitat conditions at
some population sites of both species. A
peer reviewer brought the ongoing
installation of utility service
improvements with potential to impact
Texas golden gladecress in portions of
its range to our attention. Peer reviewers
also agreed that drought negatively
affects the Neches River rose-mallow,
and they provided new, detailed
information on the types of invasive
plants that most seem to constitute a
threat to the species, as well as the
extent of the invasion by these plants
into Neches River rose-mallow
population sites. In addition, they
furnished information about the
presence of feral hogs at specific Neches
River rose-mallow population locations,
as well as observations of sedimentation
from a highway construction project
into one Neches River rose-mallow site.
One peer reviewer indicated his
agreement that the Neches River rosemallow lacks protective mechanisms
other than U.S. Army Corps of
Engineers (USACE) permits. One peer
reviewer expressed his opinion that we
needed more pertinent geological
information on the outcrops across a
larger geographic area than just
Nacogdoches, San Augustine, and
Sabine Counties. He also suggested
chemical analysis of the outcrops
known to support the Texas golden
gladecress so as to better understand
their unique qualities in order to use
that information to seek out additional
sites to survey for heretofore
undiscovered populations or to carry
out recovery actions.
We also solicited information from
the general public, nongovernmental
conservation organizations, State and
Federal agencies that are familiar with
the species and their habitats in east
Texas, academic institutions, and
groups and individuals that might have
information that would contribute to an
update of our knowledge of the Texas
golden gladecress and the Neches River
rose-mallow, as well as the activities
and natural processes that might be
contributing to the decline of either
species. We used information garnered
from this solicitation in addition to
information in the files of the Service,
TPWD, TXNDD’s elements of
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occurrence records for both species,
published journal articles, newspaper
and magazine articles, status reports
contracted by the Service and TPWD,
reports from site visits, and telephone
and electronic mail conversations with
knowledgeable individuals. We also
used satellite and aerial imagery to
ascertain changes in land cover and
land use at historical population sites
and to determine whether changes in
land cover and land use at historical
populations sites and to determine
whether the presence of primary
constituent elements for each species
were still in place. Additionally, we
used the results of population
monitoring from site visits to look at
abundance, and if enough information
was available, to get an idea of trends in
the populations. In October 2011, we
also made field trips to known sites
where we were granted access, to verify
land uses and contribute to the veracity
of our threats analysis. In March 2012,
we helped to organize and carry out a
workshop and field tour of Texas golden
gladecress sites for purposes of assisting
landowners and agricultural agencies to
become familiar with the species and its
habitat. We also revisited accessible
Texas golden gladecress sites at that
time. In August 2012, we attended a
Neches River rose-mallow workshop
and field tour conducted by TPWD and
revisited Neches River rose-mallow
population sites. We used the best
scientific and commercial information
available in assessing population status,
recognizing the limitations of some of
the information.
(24) Comment: There is no conclusive
indication that glauconite quarrying, oil
and gas activities, invasive species, or
pine tree plantings threaten Texas
golden gladecress.
Our Response: As stated in the
proposed rule and this final rule, three
historical populations of Texas golden
gladecress were documented from sites
where glauconite quarries are now
located. The sole introduced Texas
golden gladecress population, in
Nacogdoches County, was extirpated by
construction of a pipeline as recently as
2011. The Weches glades are
documented to be overgrown with
invasive, native and nonnative plants.
The potential for negative effects from
pine trees, planted in such close
proximity to glades that shading and
leaf litter accumulations adversely affect
the glades, was pointed out to us by
several respondents during the
comment periods on the proposed rule,
as well as one of our peer reviewers
based on their personal observations
(see the Summary of Factors Affecting
the Species section of this final rule).
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(25) Comment: There is no conclusive
indication that the invasion by other
species, development and construction
projects, herbicide use, or herbivory
pose a risk of loss or degradation to the
Neches River rose-mallow.
Our Response: A thorough analysis of
the impacts of nonnative and native
species encroachment, TXDOT roadway
construction and maintenance projects,
herbicide use, and herbivory were
discussed in the proposed rule and in
this final rule. All populations of the
Neches River rose-mallow have been
encroached upon by Chinese tallow.
This invasive species is fast-growing
and, once established in a habitat, is
highly destructive, choking out native
species. Development and construction
projects will likely continue to be a
threat to the species. Herbicides are a
threat that could impact 7 of 11 (64
percent) Neches River rose-mallow
populations. We do not consider
herbivory to be a threat to the Neches
River rose-mallow at this time. See the
Summary of Factors Affecting the
Species section of this final rule for our
complete evaluation.
(26) Comment: The best available
information stated that the Texas golden
gladecress and the Neches River rosemallow are resilient species.
Our Response: Based on our review of
the best available scientific and
commercial data, we concluded that the
Texas golden gladecress exhibits low to
moderate resiliency. Although the
species has persisted at several sites in
the face of bulldozing, drought, and
invasion by woody species, likely due to
its persistent seed bank, and has also
stayed in existence in small sites with
small numbers of individuals, perhaps
due to self-fertilization, it has shown no
resiliency to impacts such as
excavations (e.g., quarrying) and
pipelines. For more information, see the
Determination section of this rule. In the
case for the Neches River rose-mallow,
the best available scientific information
indicates that, while reductions in the
species’ range have not occurred, there
have been significant impacts from
habitat modification and loss that have
caused reductions in most, if not all, of
the known Neches River rose-mallow
populations. The Neches River rosemallow is adapted to highly variable
rates of water flow, including seasonal
high and low flows, and occasional
floods and droughts. However, as the
habitat is so water-dependent, threats
that could adversely modify its habitat,
including invasion from nonnative and
native woody vegetation, hydrological
changes, herbicide, trampling, and
drought, can have huge impacts. The
Neches River rose-mallow likely
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requires high precipitation and flowing
water or flood events to disperse seed
(Warnock 1995, p. 20; Scott 1997, p. 8;
Reeves 2008, p. 3), and although the
Neches River rose-mallow is adapted to
persisting during dry portions of the
year, a complete lack of water can
diminish seed production, range
expansion, and genetic exchange.
(27) Comment: The Texas golden
gladecress is already adequately
protected by co-existing with the
federally listed white bladderpod and
collaborations between the Service and
several partners.
Our Response: White bladderpod is
found at two of the remaining known
Texs golden gladecress population sites
(see our response to Comment 22). Both
sites are privately owned with the
exception of the Texas golden
gladecress plants that extend onto the
Sunrise Road ROW at Caney Creek
Glade Site 1; therefore, absent a Federal
nexus, no legal protections are afforded
to either species under the Act. The
Chapel Hill landowner does mow or
bush-hog at least once per year to try to
keep woody plants from overrunning
this small tract, but this action is strictly
voluntary on his part and not assured
into the future.
(28) Comment: The mechanisms and
plans provided by the Davy Crockett
NF, the TXDOT, groundwater
management areas and conservation
districts, federally protected wetlands,
and a number of private initiatives and
agreements all serve to adequately
protect the Neches River rose-mallow
species.
Our Response: We agree that the
Neches River rose-mallow does benefit
from some protections on USFS and
TXDOT lands. As of the effective date
of this rule (see DATES), the Neches
River rose-mallow is a federally listed
threatened species. Further, we are
publishing a final rule on designation of
critical habitat for the Texas golden
gladecress and the Neches River rosemallow under the Act elsewhere in
today’s Federal Register. Therefore, if a
Federal nexus exists for a project,
projects within the species’ range or
within designated critical habitat units
must avoid jeopardizing the species or
adversely modifying its designated
critical habitat.
(29) Comment: Local elected officials
were not notified of the proposed
designation during the public comment
period. It is crucial that the Service
contacts potentially impacted private
landowners, local elected officials and
leaders, and industry in these counties.
Our Response: We made substantial
efforts to notify the public and
interested parties, as described here. We
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announced the opening of the public
comment period on the proposed rule in
Nacogdoches, Houston, and Harrison
Counties via newspaper public notices
on September 19 and 20, 2012. Within
14 days post-publication of the
proposed rule in the Federal Register,
the Service mailed 164 letters to
recipients that included both U.S.
senators; the U.S. representative from
east Texas; two State senators and three
State representatives for the districts in
question; and the county judges and all
four commissioners from each of the
following counties: Sabine, San
Augustine, Nacogdoches, Houston,
Cherokee, and Trinity. We also notified,
via letter, State officials including the
Texas Governor, State Comptroller,
Texas General Land Office (TGLO)
Commissioner, and Executive Directors
of Texas Parks and Wildlife Department
(TPWD) and Texas Department of
Transportation (TXDOT). Letters were
also sent to staff of interested or affected
agencies (TPWD, Texas Council of
Environmental Quality, TXDOT, Texas
Railroad Commission, Texas General
Land Office, Texas Forestry Service,
Texas Department of Agriculture, U.S.
Department of Agriculture’s Natural
Resources Conservation Service,
USACE), universities, conservation
organizations and other
nongovernmental organizations, and
representatives of the following
industries: Glauconite quarries, oil and
gas exploration and production, timber
production, and forestry services. In
addition, we sent letters to some
landowners, including private
individuals, USFS, and TXDOT.
More specifically with regard to
landowners, in September 2011,
approximately 1 year prior to
publication of the proposed rule, we
sent letters to 107 entities, including
representatives of many of the agencies
or organizations listed above, informing
the recipients of our need to gather and
analyze the best available information
for our use in developing a proposed
rule to list and designate critical habitat
for both species. We then added any
landowner contacts that were given to
us to our notification list. For some
sites, landownership was clarified in
file records or through communications
with representatives of other
organizations. Furthermore, for the
Texas golden gladecress, we partnered
with TPWD in March 2012, to host a
Weches Glades workshop and field tour
in San Augustine, to which we invited
four private landowners (two with
Texas golden gladecress and two with
white bladderpod populations on their
property). As preparation for the field
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tour, permission to access sites was
obtained from these four landowners.
The purpose of the workshop and field
tour was to acquaint landowners, and
agency representatives that work with
private landowners, with the glade and
outcrop habitats, rare plants, and the
listing process and implications,
particularly as it applies to plants. In
addition to these landowners, 24 other
individuals were invited to the
workshop, including two San Augustine
County commissioners; the Mayor of
San Augustine; the Chairman of the
local Soil and Water Conservation
District; and individuals from the
Natural Resources Conservation Service,
Texas Forest Service, a private forestry
services company, and a mining
company. Of the 28 invitees, 17
attended the workshop and field tour.
As additional outreach to Neches
River rose-mallow landowners, land
managers, and agencies that work with
them, TPWD organized a workshop and
2-day field trip in August 2012. The
workshop also furnished an opportunity
to explain the listing process and its
applicability for plants. A pre-field trip
workshop allowed information to be
presented to 45 attendees that included
the Texas Land Conservancy (owner of
the Neches River rose-mallow Lovelady
site) and TXDOT (owner of the ROW
sites along SHs 204 and 94).
On April 16, 2013, the day of Federal
Register publication of the document
making available the draft economic
analysis and reopening the comment
period for the proposal to list the plants
and designate critical habitat, we
emailed letters to 157 people including
representatives of agriculture, timber,
oil and gas, and mining industries; local
elected officials from the counties in
question; agency staff that work with
landowners; and those landowners for
whom we had email addresses. Within
2 days of publication in the Federal
Register, we also sent 208 letters by
mail to State and local elected officials
(including all county judges and
commissioners); industry
representatives; scholars; conservation
organizations; State, Federal, and local
agencies; and all individual landowners
who had been identified through the
past 2 years since our initial information
solicitation in September 2011.
(30) Comment: Multiple State entities
expressed concerns that these listings
will hamper economic development.
They indicated their belief that listing
could impact agriculture and timber
planting operations; oil and gas
operations; and highway construction
and maintenance projects in
Nacogdoches, Sabine, and San
Augustine Counties. They were
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concerned that projects with a Federal
component could be delayed or
cancelled in the listed counties. They
also indicated concern that listing could
impact ground water management,
reservoir construction, road and bridge
projects, and agriculture operations in
Cherokee, Harrison, Houston,
Nacogdoches, and Trinity Counties.
Our Response: Under section
4(b)(1)(A) of the Act, we must base a
listing decision solely on the best
scientific and commercial data
available. The legislative history of this
provision clearly states the intent of
Congress to ensure that listing decisions
are ‘‘. . . based solely on biological
criteria and to prevent non-biological
criteria from affecting such decisions
. . . ’’. Therefore, we did not consider
the economic impacts of listing these
species. See our response to Comment
12.
With respect to effects of listing on
highway construction and maintenance,
TXDOT has formally consulted with the
Service only once for the white
bladderpod in the 26 years that the
plant has been listed. This formal
consultation took place in 2009, for a
highway safety improvement project on
approximately 10 miles (16.1 km) of SH
21. The consultation resulted in slight
modifications to TXDOT’s original plan
for a 4-ft (1.2-m) widening of the
shoulder, instead widening it to 3 ft (0.9
m) for a short distance around a white
bladderpod population. The Service and
TXDOT agreed to creation of a ‘‘No
Work Area’’ around the white
bladderpod during construction phases
to protect the plant from foot and
vehicle traffic and to prevent any
staging of equipment or materials.
Provisions were made for TXDOT to
continue maintenance (mowing) within
the No Work Area post-project during
the plant’s dormant season (July 1 to
August 31). The TXDOT also agreed to
enhance habitat by hydroaxing invading
woody vegetation at three white
bladderpod sites on private land as
compensation for loss of one or more
plants that could not be avoided. These
are the types of recommendations that
are anticipated in the few situations
where Texas golden gladecress occurs in
State-maintained ROWs. The TXDOT
has indicated that they do not have
major highway construction projects
planned anywhere near the critical
habitat within the next 20 years, so we
do not anticipate delays of highway
construction projects.
(31) Comment: Although Neches
River rose-mallow is considered
extirpated in the SH 230 ROW, in 2012,
Laura Baker, a graduate student at
Stephen F. Austin State University,
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reported seeing Neches River rosemallows within the ROW somewhere
near the former site (Baker 2012, pers.
comm., in Melinchuk 2012, p. 3). This
observation needs to be verified.
Our Response: We visited the site
along SH 230 in Houston County in
2011, and did not find any Neches River
rose-mallow plants. This site was
considered extirpated due to herbicide
overspray along the ROW. However,
based on this comment, the population
could still be present. Another
commenter provided information
regarding reintroduced populations near
the cities of Douglass and Chireno, and
at the Pineywoods Native Plant Center,
all in Nacogdoches County. These
populations need to be verified as
Neches River rose-mallow and not a
hybrid variety.
(32) Comment: The Neches River rosemallow and the other two co-occurring
Hibiscus species are wetland rather than
aquatic plants. They do not grow in
permanently standing water. They grow
near permanent or ephemeral water
bodies, and the sites are occasionally
flooded. For most of their life cycle they
grow on saturated soils that can become
surficially dry. The proposed rule (77
FR 55973) states that the Neches River
rose-mallow prefers deeper water; it
would be more correct to say that the
plants prefer areas near deeper water.
Our Response: In our proposed rule at
77 FR 55973, we state, ‘‘Geographically,
these three species [the halberdleaf,
crimsoneyed, and Neches River rosemallows] can be found within similar
habitats, but the halberdleaf and the
crimsoneyed rose-mallows prefer deeper
water and are found along edges of
major rivers and streams (Blanchard
1976, pp. 10–14; Poole 2011b, pers.
comm.), compared with the [Neches
River] rose-mallow, which is found in
side channels and floodplains of major
river drainages.’’
Neches River rose-mallow is an
endemic east Texas wetland species,
occupying relatively open habitat. Soils
are of the Inceptisol or Entisol orders
(Diggs et al.2006, pp. 46, 79) and,
although generally water-saturated, can
often be surficially dry. Geographically,
the Neches River rose-mallow and the
two other co-occurring Hibiscus species
can be found within similar habitats;
however, the Neches River rose-mallow
prefers areas near deeper water, whereas
the halberdleaf and crimsoneyed rosemallows are found along edges of major
rivers and streams (Blanchard 1976, pp.
10–14; Poole 2011b, pers. comm.).
(33) Comment: The general habitat for
the Neches River rose-mallow is more
similar to seasonally flooded river
floodplains (Diggs et al. 2006, pp. 103–
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104) rather than the short-leaf or
loblolly pine-hardwood forest, longleaf
pine, or loblolly pine forest (77 FR
55973).
Our Response: As stated in the
proposed rule, Gould (1975, p. 10) and
Correll and Johnston (1979, p. 1030)
described the generic vegetation
community of the Neches River rosemallow as the Pineywoods of east
Texas. Diggs et al. (2006, pp. 2–3) also
describes the generic geographic area as
the Pineywoods; however, this was not
mentioned in the proposed rule. More
specifically, Neches River rose-mallow
habitat within the Pineywoods is more
accurately classified by Diggs et al.
(2006, pp. 103–104) as ‘‘seasonally
flooded river floodplains.’’ Natural
bottomlands occupy the flat, broad
portions of the floodplains of major
rivers and are seasonally inundated
with loamy to clayey seasonally flood
and host flood-tolerant species of oak,
sweetgum, elm, swamp tupelo, and red
maple (Diggs et al. 2006, p. 103). Stands
of shortleaf, longleaf, and loblolly pine
are not occupied by the Neches River
rose-mallow.
(34) Comment: The proposed rule
states that flowing water is required for
seed dispersal downstream (77 FR
55974, 55988). However, research
suggests this process has not entirely
been investigated. Warnock (1995) notes
that seed dispersal of Neches River rosemallow is probably by water, Scott
(1997, p. 5) stated that seed dispersal
appears to be entirely water dependent,
and Reeves (2008) discusses the
dispersal of Hibiscus moscheutos
(including lasiocarpos). The commenter
states that although water-mediated
seed dispersal of the Neches River rosemallow is highly likely, it is not known
that flowing water is required for seed
dispersal downstream.
Our Response: We agree that based on
the best scientific and commercial data
available, Neches River rose-mallow
seeds are likely to be dispersed by
flowing water. This change is reflected
in the ‘‘Habitat’’ section for the Neches
River rose-mallow of this final rule, yet
this comment did not change our listing
determination for the Neches River rosemallow.
(35) Comment: Of the four introduced
populations of Neches River rosemallow, all but the experimental site
(which has been manipulated) have
experienced population declines (50
percent in Davy Crockett NF
compartment 20, 90 percent in Davy
Crockett NF compartment 16, and 95
percent in Davy Crockett NF
compartment 11). Rapidly declining
populations such as those in Davy
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Crockett NF compartments 16 and 11 do
not appear viable.
Our Response: The Act requires us to
determine if the Texas golden gladecress
and Neches River rose-mallow warrant
listing based on our assessment of the
five listing factors described in the Act
using the best scientific and commercial
data available at the time we conduct a
review of the species. As part of our
assessment, we evaluate whether a
threat(s) is causing declines in numbers
of individual plants in all populations
or in specific population sites. However,
a population’s viability in and of itself,
if not influenced by specific threats, is
not a factor considered in our
evaluation.
(36) Comment: One commenter noted
that several of the population estimates
throughout the proposed rule were not
accurate or consistent. Information
pertaining to sites 2, 3, 6, 7, and 8 in
Table 4 of the proposed rule needs to be
changed. Site 2 states 78 plants were
counted in 2003, but this should read
stems. Site 3 states that 200–250 Neches
River rose-mallow plants were
introduced on compartment 20 of the
Davy Crockett NF in 2000; however, the
critical habitat section (Critical Habitat
Unit 7) states that 350–400 plants were
introduced in 2000. The actual number
introduced is important in evaluating
the success of the reintroduction. Site 8
states several hundred plants were
counted in 2001, but this should read
several hundred flowers. Site 7, the SH
204 ROW site, has had as many as 75
individuals, not a maximum number of
seven plants.
Our Response: The language in Table
4 pertaining to site 2 (compartment 16
of the Davy Crockett NF) has been
updated. Site 2 (compartment 16) and
Site 4 (compartment 20) were planted in
2000 (Nemec 2000, p. 3), totaling 700
plants in both units, with about 450
plants in Site 2 and about 200–250
plants in Site 4. Site 6 (SH 204) has been
observed with about 75 plants in 1997,
its maximum count to date, and this
change is reflected in this final rule.
(37) Comment: One commenter noted
the steep decline in the reintroduced
site in compartment 16 of the Davy
Crockett NF where the population has
decreased by 90 percent (from 450 to 43
plants). Whether the loss of the beaver
dam resulted in this drastic decrease
needs further study.
Our Response: See our response to
Comment 19.
(38) Comment: In the proposed rule
under the heading ‘‘Trampling by Feral
Hogs and Cattle’’ (77 FR 55987), it states
that because Neches River rose-mallow
habitat is permanently or temporarily
flooded, feral hogs have limited access
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to the plants. Neches River rosemallows do not occur in permanently
standing water, although they may grow
adjacent to such sites. Their habitat is
only flooded infrequently. For most of
the year, it is surficially dry and easily
disturbed by feral hogs. The commenter
also noted feral hog damage of Neches
River rose-mallow (breaking and
flattening) at the introduction site in
compartment 20 on the Davy Crockett
NF (TXNDD 2012a).
Our Response: National Wetland
Inventory (NWI) maps were used to
verify habitat at each Neches River rosemallow site. Compartment 20 was
described on the NWI map as
permanently or temporarily flooded
habitat. The Service recognizes that
Neches River rose-mallow prefers areas
located near deeper water, generally
with temporary not permanent standing
water. The long-term impact on the
Neches River rose-mallow from feral
hog damage is unknown. Feral hog
presence has been limited to five
Neches River rose-mallow sites with
minimal damage to habitat. The Service
considers feral hogs a present threat and
one that will likely continue into the
near future. However, at this time, the
severity of impacts to the species is low.
This threat does not change the
determination to list the species as
threatened versus endangered. See also
our response to Comment 18.
(39) Comment: The listing proposal
states that no genetic studies have been
conducted on the Neches River rosemallow; however, there have been two
such studies by Klips in 1995 and
Mendoza in 2004. Neither study looked
at genetic drift, inbreeding, or the
possible threat from hybridization. It
seems premature to conclude that small
population size and hybridization are
not potential threats.
Our Response: The Service has
reviewed Klips (1995, entire) and
Mendoza (2004, entire) and
incorporated this information into our
analysis in the Summary of Factors
Affecting the Species section of this
final rule. While these studies pertain to
genetic analysis, they do not look at
genetic drift, inbreeding, or the possible
threat from hybridization, as the
commenter acknowledges. Based on the
best scientific and commercial data
available, we do not consider
hybridization or small population size a
threat to the species at this time. See our
response to Comment 11 for additional
information regarding this comment.
(40) Comment: Listing of the two
plants will have adverse impacts on the
State transportation system other than
in instances where they occur in or
immediately adjacent to State-owned
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ROW. Listing will hamper economic
development and delay projects that
require section 7 consultations.
Our Response: See our response to
Comment 30 above.
(41) Comment: There are existing
mechanisms that adequately protect
both species.
Our response: See our response to
Comments 22, 27, and 28.
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Federal Agency Comments
(42) Comment: The Natural Resources
Conservation Service indicated their
willingness to assist landowners and
land managers in identifying those
elements that may have a negative or
positive impact on the species.
Our Response: We appreciate the
Natural Resources Conservation
Services’ (NCRS’) willingness to help
landowners with actions to conserve
these species. We foresee that NRCS’
assistance to landowners and to the
Service will be invaluable in delivering
conservation programs like the Service’s
Partners for Fish and Wildlife Program
that can help willing landowners plan
and implement projects to restore
habitat for both of these plant species.
Public Comments
(43) Comment: One commenter
provided information regarding
reintroduced populations near the cities
of Douglass and Chireno, and at the
Pineywoods Native Plant Center, all in
Nacogdoches County. These
populations have not been verified by
the Service or a species expert. These
populations need to be verified as
Neches River rose-mallow and not a
hybrid variety.
Our Response: These populations
have not been verified by the Service or
species experts. Until such verification,
the Service cannot use this information
in our analysis.
(44) Comment: Several commenters
expressed their beliefs that these species
have not been fully studied. They
indicated that there are significant
concerns with the quality of data and
analysis the Service used for its
determination. They believe that the
proposal is based largely on
inconclusive reports and vast
speculation about operations thought to
affect habitats, existing regulatory
mechanisms, conservation efforts,
species populations, and potential
threats that fail to provide any sound
scientific foundation on which to justify
the listing of these species. Other
commenters assert that the Service does
not have the scientific justification to
list these species.
Our Response: See our response to
Comment 23.
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(45) Comment: As outlined in the
2003 St. Augustine Glades Conservation
Area Plan, TNC, along with other
resource professionals, identified the
conservation concerns and challenges
for sustaining populations of the Texas
golden gladecress.
Our Response: We were aware of this
document and considered this in our
preparation of this determination.
(46) Comment: A commenter
recommended that the benefits provided
by conservation efforts currently in
place in an area be fully considered.
Our Response: Section 4(b)(1)(A) of
the Act requires us to take into account
those efforts being made by a State or
foreign nation, or any political
subdivision of a State or foreign nation,
to protect such species. We consider
relevant Federal, State, and tribal laws
and regulations when developing our
analysis. Regulatory mechanisms may
preclude the need for listing if we
determine such mechanisms adequately
address the threats to the species such
that listing is no longer warranted.
However, existing regulatory
mechanisms are inadequate to protect
these species, and the ongoing
conservation efforts are not sufficient to
remove the threats to these species.
Please see ‘‘Other Conservation Efforts’’
under ‘‘A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range’’ for
the Texas golden gladecress and Neches
River rose-mallow in this final rule.
(47) Comment: Multiple commenters
believe that interested parties should be
given sufficient opportunity to review
and comment on any proposal,
including review of scientific data from
an independent specialist’s economic
analysis of the current proposal, before
the Service makes a final decision in
this rulemaking. Similarly, any data
provided to Service during future public
hearings should also be made available
to the public for review and comment.
Our Response: This information was
provided to the public for review and
comment. Please see our response to
comment 29 above for a full description.
(48) Comment: One commenter
recommended that any proposal to list
a species should include easily
accessible and transparent information
about cited literature. Another
commenter noted that Executive Order
13463 directs agencies to provide timely
online access to the rulemaking docket
on https://www.regulations.gov,
including relevant scientific and
technical findings, in a format that can
be easily searched and downloaded
(E.O. 13463, sec. 2(b)). The proposed
rule failed to provide a meaningful
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opportunity to understand and
comment on the Service’s proposal.
Our Response: Executive Order
13463, signed by the President on April
18, 2008, amends Executive Orders
13389 (Creation of the Gulf Coast
Recovery and Rebuilding Council) and
13390 (Establishment of a Coordinator
of Federal Support for the Recovery and
Rebuilding of the Gulf Coast Region).
None of these three Executive Orders
directs Federal agencies to provide
timely online access to the rulemaking
docket. We believe the commenter is
referring to Executive Order 13563,
‘‘Improving Regulation and Regulatory
Review,’’ and we believe that we have
met the direction of that Executive
Order. For our proposed rule to list the
species and designate critical habitat,
we provided the literature cited
bibliography on https://
www.regulations.gov when we
published the proposed rule. The
proposed rule also stated that additional
tools and supporting information that
we developed for that proposal were
available at the Service’s field office in
Corpus Christi by appointment or that
arrangements could be made to get that
information by calling the field office.
For this final determination, the
literature cited bibliography and all
tools and supporting information are
available at:
• https://www.regulations.gov under
Docket No. FWS–R2–ES–2012–0064,
• https://www.fws.gov/southwest/es/
ElectronicLibrary/ElectronicLibrary_
Main.cfm,
• https://www.fws.gov/southwest/es/
ClearLakeTexas, and
• Texas Coastal Ecological Services
Field Office in Corpus Christi (see
ADDRESSES).
(49) Comment: The Service’s failure to
examine relevant evidence, explain its
assumptions, consider contrary
evidence in the studies on which it
relies, identify uncertainties, share the
studies it relied upon, and utilize basic
scientific principles in its predictive
analysis is arbitrary, capricious, and not
in accordance with the law. There is no
basis in the record to support listing the
plants under the Act.
Our Response: As we are unable to
identify from this comment the specific
assumptions or contradictory evidence
that the commenter is referring to, we
cannot adequately provide a response to
that part of this comment. We assessed
the status of both species using the best
scientific and commercial data
available. We obtained this information
by reviewing the candidate assessments
that had been done for each species
since they were first determined to be
warranted for listing (in 1975 for the
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Neches River rose-mallow, and in 1997
for the Texas golden gladecress), using
all information in our files, soliciting
new information prior to publication of
the proposed rule, as well as during two
comment periods, from a wide variety of
knowledgeable entities and individuals,
and using additional sources of
information such as peer-reviewed
journals and other publications. We
incorporated all substantial information
we received into this final rule,
including any new information
regarding the species’ status, habitat
conditions, and threats. We believe that
we did identify and point out
uncertainties and data gaps. We had to
rely on the best scientific and
commercial data available to us, as
opposed to collecting new data to fill
gaps. We believe that we have made a
sound case for why the Texas golden
gladecress warrants listing as
endangered and the Neches River rosemallow warrants listing as threatened
under the Act. For further information,
see our response to Comment 23.
(50) Comment: The threat to SH 204
ROW by ‘‘water management strategies’’
is speculative. There are no scientific
data that demonstrate the level of
hydrological change that would impact
the Neches River rose-mallow; the
Service is speculating this threat. Also,
the proposed rule’s discussion of the
plant numbers for the Neches River
rose-mallow and the impacts of the
proposed Lake Columbia project on this
species have not been subjected to
rigorous scientific analysis or
discussion. The Service does not report
on information from two of its
published reports; specifically plant
count information was missing from
2007. Also, in these reports, plants were
determined to be Hibiscus hybrids;
however, this was not mentioned. There
is no explanation of why the Service did
not present this readily available data.
Our Response: Some degree of
hydrological change has been seen at
most of the Neches River rose-mallow
sites; however, information on some of
the private land sites is lacking. Many
wetland species, including the Neches
River rose-mallow, are adapted to highly
variable rates of water flow, including
seasonal high and low flows, and
occasional floods and droughts. For
example, the Neches River rose-mallow
likely requires high precipitation and
flowing water or flood events to
disperse seed (Warnock 1995, p. 20;
Scott 1997, p. 8; Reeves 2008, p. 3), and
although the Neches River rose-mallow
is adapted to persisting in dry
conditions during portions of the year,
a complete lack of water can diminish
seed production, range expansion, and
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genetic exchange. As Niches River rosemallow habitat is so water-dependent,
hydrological changes can have huge
impacts.
In regards to the SH 204 ROW site, the
best scientific and commercial data
available suggest that the construction
of the Lake Columbia reservoir project
will divert water downstream, thereby
likely dewatering the site. The agencies
involved with the project are still
working on solidifying the project
details, and, therefore, we do not know
how much water will remain at this site
or if future water management practices
or decisions will allow for seasonal
flooding of water to this site. Please
reference the ‘‘Hydrological Changes’’
section in this rule for more information
on this project and hydrological impacts
to this and other sites.
Summary of Changes From Proposed
Rule
There are not any substantial changes
from the proposed rule. We did receive
new information regarding the presence
of feral hogs at Neches River rosemallow sites. Based on this new
information, we determined that feral
hogs are a current and continuing threat
to the Neches River rose-mallow, but the
severity of the threat is low. We also
received new information about ongoing
service line improvements, including
communication, domestic gas, water,
sewer, and electric lines, that were
occurring within the Texas golden
gladecress’s range, sometimes in
highway ROWs. We determined that,
because these improvements may
involve excavations of habitat and
plants, they could constitute additional
threats to the Texas golden gladecress.
These newly identified threats do not
alter our listing determinations.
Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1533),
and its implementing regulations at 50
CFR part 424, set forth the procedures
for adding species to the Federal Lists
of Endangered and Threatened Wildlife
and Plants. Under section 4(a)(1) of the
Act, we may list a species based on any
of the following five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; and (E)
other natural or manmade factors
affecting its continued existence. Listing
actions may be warranted based on any
of the above threat factors, singly or in
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combination. Each of these factors is
discussed below.
Texas Golden Gladecress
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Habitat loss and degradation have
been the primary cause of decline in
Texas golden gladecress during the last
two decades. Permanent removal or
destruction of habitat by quarrying and
pipeline installation projects has
eradicated several populations. Other
habitat alterations that are occurring
across the species’ range, with potential
to destroy or negatively alter Texas
golden gladecress’s habitat, include
construction of well pads, buildings,
roads, and poultry production facilities,
and service line improvements. A
historic and ongoing major threat to
Texas golden gladecress’s habitat is the
invasion by nonnative and native
shrubs, trees, and vines, and other
weedy species into the formerly opensun, herbaceous, glade vegetation
communities. Planting of pine
plantations can potentially have
negative impacts on the Texas golden
gladecress if the spacing of planted trees
puts them in close proximity to
occupied outcrops, resulting in shading
and pine leaf litter accumulations in the
glade habitat. Grazing has been
implicated as a habitat threat because it
is often associated with the
encroachment of undesirable vegetation
into the outcrop habitat, and may lead
to trampling of plants. Agricultural
herbicide use has some potential to
damage emerging Texas golden
gladecress seedlings. Severe and
extended periods of drought,
anticipated to increase with projected
changes in the climate, may negatively
affect a given year’s reproductive effort
by Texas golden gladecress. These
factors will be discussed in more detail
below.
Glauconite Quarrying (Mining)
Glauconite, often called ‘‘blue rock’’
or ‘‘green rock,’’ is used in San
Augustine and Sabine Counties for road
construction and maintenance by
county road departments, USFS, and
Louisiana Parishes (McGee 2011, pers.
comm.). Glauconite has also been used
by the oil and natural gas industry for
roads and well pads, and demand by the
oil and gas industry is high (McGee
2011, pers. comm.). Glauconite is also
used as a component of fertilizer and as
an animal feed additive (Godwin 2012,
pers. comm., p. 4). A number of
commercial glauconite quarries or
mines were in production by 1997, and
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subsequent interest in its use grew
because traditional pavement base
materials historically used in this region
(iron ore and limestone) were becoming
harder to obtain and more expensive
(Button and Little 1997, p. 14). A
representative of one mining company
with four quarries in the San Augustine
and Sabine County area expressed an
opinion that their mines were
sustainable for 15 to 20 years at the
current level of demand (McGee 2011,
pers. comm.). The best scientific and
commercial information available does
not allow us to make predictions about
future demand for glauconite, and we
are unable to project the level of future
quarry development throughout the
Texas golden gladecress’s range.
Selection of quarry sites can be based on
different site qualities and the variation
in the mineral composition of the
Weches Formation across its geographic
range. Selection of locations for
glauconite quarries may target areas
‘‘where the glauconite can be seen on
the surface’’ (outcrops), although
quarries have also been dug on sites
where the glauconite was not visible at
the surface (McGee 2011, pers. comm.).
TNC (2003, p. 9) noted that glauconite
quarrying (mining) in glades destroys
habitat and is a significant threat to the
Texas golden gladecress. The majority of
known habitat was excavated at three of
the eight historical populations (Caney
Creek Glade Sites 2, 6, and 8) between
1996 and 2011, resulting in open pits at
the former habitat sites. The excavations
removed all surface features required by
the gladecress, as well as killing
individual plants. The Service has been
denied access to these sites; thus we
cannot determine if any habitat or
plants remain on the periphery of the
excavated quarries. The last recorded
survey of plants at Caney Creek Glade
Site 2 was on March 18, 1988, when the
Texas golden gladecress plants were
described as growing on the sloping
Weches outcrop that was brush-hogged
and burned in 1988. Using available
high-altitude photography taken
between 1995 and 2009, supplemented
with aerial photography from August
2010, it appears that the glade was still
intact as of 1995–1996, but that a much
larger area than the original population
site was excavated by 2005. As of 2010,
the entire population site and
surrounding area looks to be two large,
side-by-side pits or ponds. Based on the
total loss of habitat (surface and
subsurface) due to the excavation, over
a large portion of the former population
site, we assume that the population was
extirpated here.
The last information on plant
numbers and conditions at the Caney
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Creek Glade Sites 6 and 8 was collected
on March 19 and April 24, 1987. At that
time, Caney Creek Glade Site 6 was
recognized as the largest known viable
population of Texas golden gladecress.
At this site, the Texas golden gladecress
grew in a former pasture with thousands
of fruiting plants in association with
other native glade plants, including
white bladderpod, in shallow bedrock
pockets. The Caney Creek Glade Site 8
consisted of a very small population on
a degraded Weches outcrop, with
scattered plants in fruit. Both elements
of occurrence appeared to be eliminated
by a large, open-pit quarry in which
digging started after 1996, with the
entire area being one large pit by 2009.
The outcrops may actually attract
glauconite quarrying interests because
the presence of an outcrop indicates that
glauconite is close to the surface.
Glauconite mining can occur throughout
the range of Texas golden gladecress
and has the potential to eradicate
populations at sites where quarries are
dug. There is no requirement for permits
to develop a quarry, typically there is no
Federal nexus, and locations of future
quarries are unknown. Based on our
review of the scientific information, we
conclude that excavation of pits for
removal of glauconite, and associated
glauconite-quarrying activities, pose a
threat to the Texas golden gladecress
across the species’ range.
Natural Gas and Oil Exploration and
Production
A principal threat to the habitat of
Texas golden gladecress is the removal
or destruction of habitat (outcrops and
immediate surrounding land) by
pipeline construction or from
construction of buildings, well pads, or
roads to access drilling sites directly
over habitat. Natural gas pipeline
installation requires trenching and
clearing that can destroy all gladecress
habitat and plants within the pipeline
ROW. In addition to the destruction of
habitat, excavation could conceivably
alter the hydrology of Texas golden
gladecress sites if the lowered elevation
of the excavation, or conversely, the
increased ground elevation of a well pad
or other structure, diminishes the
amount of water that can move
downslope over ground or through
seeps. Adversely affecting the amount
and timing of water delivery could
render outcrop ledges uninhabitable for
the species by interfering with the
seeping or pooling action of water on
which the species depends.
The loss of habitat and plants in the
footprint of well pads and roads built
for natural gas or oil exploration and
production is a continuing threat
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because there is high potential to affect
remaining glade habitat throughout the
species’ range. Numerous wells can be
seen from SH 21 between the cities of
Nacogdoches and San Augustine, with
at least 30 wells visible along a 20-mile
(32-km) stretch of this road (Loos 2011,
pers. comm.; Rodewald 2011, pers.
comm.). The materials brought in to
construct well pads and roads can
directly cover habitat and plants,
causing partial or total loss of
populations. Excavations, as well as
construction activities, that occur
upslope of Texas golden gladecress
populations may act to impede
movement of water downslope, thereby
interfering with seeping and pooling of
water needed by Texas golden
gladecress. Concern about the extent of
this threat is elevated due to our lack of
information about potential Texas
golden gladecress populations across
the Weches glades where surveys for the
species have not been undertaken, but
where natural gas exploration and
production is rapidly proceeding.
The entire known distribution of
Texas golden gladecress is underlain by
the Haynesville Shale formation (also
known as the Haynesville-Bossier),
recently recognized as a major natural
gas source for the United States. The
Haynesville Shale, located at a depth
exceeding 11,000 ft (3,353 m), straddles
the Texas-Louisiana border, and almost
70 percent of its production is from
wells located in Texas (Brathwaite 2009,
p. 16). The Haynesville shale covers an
area of approximately 9,000 mi2 (23,310
km2). A June 2010 map shows the
Haynesville Shale underlying the
northwestern quarter of Sabine County,
the entire northern half of San
Augustine County, and the southeastern
third of Nacogdoches County
(Haynesville Shale Map 2010).
Estimates of the natural gas contained in
this formation’s reserves indicate that it
could sustain anticipated energy needs
for well beyond the next several decades
(Hall 2009, pp. 3–7; Brathwaite 2009, p.
16). Technological improvements in
exploration (3-dimensional seismic
surveys), drilling (horizontal wells), and
well completion and stimulation
(hydrologic fracturing) have enhanced
the productive capability of natural gas
shales throughout the United States,
including the Haynesville Shale.
Natural gas exploration and
production has been rapidly expanding
within the Haynesville Shale, from the
first significant production in 2005, to
major development of the formation in
2009 (Brathwaite 2009, p. 16). Drilling
activity over the entire Haynesville
Shale peaked around 2009 or 2010,
when approximately 200 drilling rigs
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were active. As of September 18, 2011,
approximately 130 rigs were actively
drilling; the slowdown is attributed to
depressed natural gas prices (Murphy
2011a, p. 3). Even with natural gas
prices down, most companies continue
to drill one well per gas unit on the
Haynesville Shale in order to maintain
their leases (Murphy 2011a, p. 3). By
September 2011, as many as 1,500 wells
had been drilled with many more
anticipated, along with perhaps another
10 years of active drilling on this
formation (Murphy 2011b, pp. 2–3).
The Texas Railroad Commission’s
online maps (available at https://
gis2.rrc.state.tx.us/public/startit.htm)
indicate that natural gas (and some
crude oil) gathering and transmission
pipelines are found throughout
Nacogdoches County. In San Augustine
County, the majority of existing
pipelines are located in the area north
of SH 21 and west of the town of San
Augustine, an area of high glade
occurrence. To the east of San
Augustine, there are fewer pipelines,
but, of those that are located in this area,
several are large gas transmission lines.
One of these big transmission lines lies
directly adjacent to the historic Caney
Creek Glade Site 7. Sabine County has
several major interstate pipelines, but
fewer gathering and other transmission
lines than the other two counties, and
no pipelines near the Sabine County
gladecress site (Texas Railroad
Commission 2011).
The Texas Railroad Commission
regulates the oil and natural gas
industry in the State of Texas. The
Texas Railroad Commission has detailed
information on all existing pipelines,
but the agency has no way to predict
future routes for new pipelines or wells;
they are limited to location data found
within permit applications (Nunley
2011, pers. comm.). New pipelines, as
well as ones for which routes are being
determined, do not display on the Texas
Railroad Commission Web site, so
although we are aware of the impact
that pipeline excavations can have on
Texas golden gladecress, we cannot tell
where future pipelines may affect
existing populations or suitable habitat.
Loss of Texas golden gladecress
habitat and plants is inevitable if
pipelines are routed directly through
population sites. Pipeline installation
requires clearing of a path for the
pipeline, cutting a trench in which to
lay the pipe, recovering of the trench,
and restoring the ground’s surface.
Clearing pipeline pathways eliminates
obstacles to construction
(NaturalGas.Org 2011, p. 2), which may
include the rocky outcrops supporting
the Texas golden gladecress. Bulldozing
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the pipeline path likely permanently
removes these rocky ledges and other
features, along with the Texas golden
gladecress plants and seedbed. After the
pipe is put into the ground and the
trench covered with soil, elevations are
restored and the surface is revegetated,
generally using coastal bermudagrass in
this region (Rodewald 2011, pers.
comm.). The Simpson Farms Texas
golden gladecress population, located 6
mi (9.7 km) east of the city of
Nacogdoches, was eliminated by a
natural gas pipeline that was installed
sometime between August 2010 and
October 2011 (date of installation
determined from comparison of
successive years of aerial photography).
At this site, the pipeline ROW was
approximately 75 ft (23 m) wide, and
the entire area formerly occupied by the
Texas golden gladecress was covered
with deposited sediment or piles of
cleared brush (Cobb 2011, pers. comm.).
Given the degree of clearing of the ROW
and the adjacent dirt work, the known
extent of habitat is now gone, and the
entire population has likely been
extirpated (Cobb 2011, pers. comm.).
The Chapel Hill population may also be
affected by future pipeline construction;
the route for a future pipeline was being
surveyed in October 2011 (Cobb 2011,
pers. comm.). Although this pipeline
does not directly cross the very small
population site between the pasture
fence and the road, it does lie parallel
to, and just inside of, the fence line in
a pasture where Texas golden gladecress
habitat does exist (Singhurst 2012c,
pers. comm.; Singhurst 2012f, pers.
comm.).
The current trend over most natural
gas shale formations is to drill multiple
wells, when possible, and well pad sizes
can vary accordingly. Well pad sizes in
the San Augustine County area range
from several acres to as large as 14 ac
(5.67 ha), depending on the number of
wells (Loos 2011, pers. comm.; Allen
2011b, pers. comm.). Although most oil
and gas companies use existing roads,
occasionally the companies need to
build new roads, and in these cases the
new routes may go through outcrop
areas. The fill for pads and roads could
cover portions of, or potentially entire,
glade sites since some of the glades are
so small. Placement of pads or roads
upslope of Texas golden gladecress sites
may have the potential to affect
downslope movement of water to
outcrop sites (Ritter 2011b, pers.
comm.).
In summary, the remaining
populations of Texas golden gladecress
and suitable habitat are within areas
that are actively being drilled for natural
gas. Plants and habitat have been
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destroyed by the construction of
pipelines. The three remaining
populations as well as suitable habitat
are at risk of being destroyed by
construction of natural gas and oil
infrastructure (pipelines, well pads,
metering stations, and roads) that
continue to be constructed throughout
the species’ range. Exploration and
production of natural gas and oil is
anticipated to continue in this area for
at least the next decade. Texas golden
gladecress and its habitat may be
directly impacted by the construction of
pipelines and other infrastructure, and
indirectly by altering the hydrology near
occupied sites and suitable habitat.
Based on our review of the scientific
information, we conclude that natural
gas and oil development is a threat to
Texas golden gladecress.
Residential and Commercial
Construction
Although residential and commercial
construction was listed in the species’
candidate assessments as a potential
threat, there is no evidence that this
type of disturbance has directly affected
Texas golden gladecress populations.
Historically, site selection for building
homes and businesses in the town of
San Augustine may have taken
advantage of the open aspect of the
glades; Leavenworth described the area
in which he originally collected the
species (vicinity of the town of San
Augustine) as ‘‘prairies’’ (Bridges 1988,
p. II–5). However, information about
former glades in the area is lacking, as
is documentation that the Texas golden
gladecress was present where buildings
are currently located. Neither San
Augustine nor Sabine Counties are
experiencing rapid human population
growth; San Augustine County saw a 0.9
percent decline in population from
8,946 to 8,865 between 2000 and 2010,
while Sabine County had a modest
increase of 3.5 percent (10,469 to
10,834) (U.S. Census Bureau 2010a, b),
suggesting that residential and
associated commercial development
does not constitute a high level of threat
to habitat throughout the species’ range.
However, service improvements for
existing homes and businesses,
including installation of service lines for
communications, electric power, water,
sewer, and domestic gas are ongoing
and do have the potential to occur in
Texas golden gladecress habitat (Walker
2012, pers. comm., p. 1). Because water,
sewer, and gas lines entail excavations
to lay pipe, these activities could have
similar consequences to installing
natural gas and oil pipelines if the lines
pass through an occupied outcrop.
Electric power structures in this area are
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generally above-ground poles and lines
that may be installed, or maintained, in
highway ROWs. Although Texas golden
gladecress habitat and plants may
potentially be impacted by pole
placement, the small project footprint,
limited to the pole installation, may
mean that the small Texas golden
gladecress sites could be avoided by
moving pole locations a few feet to
either side of an outcrop. In those cases
where new power lines are built outside
of established ROWs, Texas golden
gladecress populations might be
damaged during clearing of habitat by
vehicles and heavy equipment
traversing a glade. However, there is
also potential that clearing of woody
vegetation out of invaded glades may
reopen them to the point that the Texas
golden gladecress could show a positive
response.
Proliferation of poultry farms was also
listed as a potential threat to Texas
golden gladecress habitat. Building
poultry production houses and
associated facilities would cover Texas
golden gladecress habitat in the same
manner as would residential or other
types of commercial construction.
Aerial photography from November
2011 (Google Earth, 2011) shows 21
poultry farms within the Texas golden
gladecress’s range (the approximate
zone of the Weches Formation) in
Sabine and San Augustine Counties. Of
the 21 total, 18 are located on the San
Augustine County Weches Formation.
None of the existing farms is adjacent to
any of the known population locations,
and we are unable to determine if any
Texas golden gladecress habitat or
plants were lost when these production
facilities were built. Among the
characteristics in east Texas that make
a site desirable for poultry production
are long, flat stretches of ground with a
good, solid hardpan as opposed to rocky
outcrops on slopes, on the tops of
ridges, or in low-lying areas (Ritter
2012, pers. comm.), such as those
occupied by the Texas golden
gladecress. This site-selection
preference means that poultry producers
would most likely avoid Texas golden
gladecress habitat. In the last 2 years,
most of the poultry farm construction
has taken place in counties north of San
Augustine and Sabine, and the only
activity in the Weches Formation zone
has been renovations to existing farms
(Ritter 2012, pers. comm.). The
construction of poultry farms is not
considered a threat to Texas golden
gladecress because poultry farm site
selection does not appear to have
significant overlap with Texas golden
gladecress habitat.
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Roads
Two of the three extant Texas golden
gladecress populations, Geneva and
Caney Creek Glade Site 1, extend into
ROWs managed by TXDOT. The third
confirmed population at Chapel Hill is
located on a small tract adjacent to a
county road and is not considered to be
in a road ROW. In the 1990s, a road
project impacted the portion of the
Caney Creek Glade Site 1 population
that occurred in the SH ROW when
Sunrise Road was widened and
straightened (Singhurst 2012g, pers.
comm.); however, not all plants were
destroyed. Review of a 2011 list of
TXDOT-planned projects did not show
any future road improvements or
expansions near known Texas golden
gladecress population sites. Based on
the best scientific and commercial
information available, we conclude that
new road construction or improvements
to the existing roads does not pose a
threat to the two Texas golden
gladecress populations that occur
within ROWs, or to the third population
that does not.
Invasive Species
A major stressor to the habitat of
Texas golden gladecress is the ongoing
invasion of nonnative and native
shrubs, trees, and vines into the
formerly open-sun, herbaceous, glade
vegetation communities. This woody,
weedy plant invasion is occurring on at
least a portion of all three remaining
population sites. The historic Caney
Creek Glade Site 7 appears, from 2010
aerial photography, to be almost 100
percent overgrown with woody
vegetation.
Glades in most parts of the United
States are declining due to grazing, fire
suppression, and the subsequent
invasion by woody vegetation. In
presettlement times, glades were
maintained by periodic fires and
browsing of woody vegetation by whitetailed deer (Odocoileus virginianus) and
elk (Cervus canadensis). This natural
disturbance regime changed over the
last century due to active fire
suppression and diminished numbers of
browsers reduced by hunting pressure
(Rossiter 1995, p. 2). Although the harsh
environment of glades helps to preclude
tree establishment, without disturbance
such as fire, woody plants will invade
(Hartman 2005, p. 4). The exclusion of
fire has allowed encroachment of trees,
shrubs, vines, and other woody plants
into glade communities (Borland 2008,
p. 3).
As woody plants mature, they
produce canopies that reduce the
amount of sunlight reaching the ground.
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Sun-loving plants like Texas golden
gladecress that are adapted to hot, dry
sites do not tolerate shade well.
Research conducted in Missouri’s cedar
glades showed that herbaceous plant
production rapidly declined when red
cedar cover exceeded more than one
third of a glade’s area (Rossiter 1995, p.
3). A combination of reduced sunlight
(shading) and increased leaf litter can
act to suppress herbaceous species
(Hartman 2005, p. 2). These types of
changes in glades that were historically
hot and dry can contribute to cooling of
the ground and enhancing of moisture
content. Wetter, cooler conditions
during traditionally hot, dry summer
months may be counter-productive for
sun-loving glade species by encouraging
invasion by cool season vegetation and
exotic species. Buildup of a deeper
organic layer can also facilitate the
establishment of woody plants that
results in further shading of the ground
(Hartman 2005, p. 2).
Invading species can also compete
directly with Texas golden gladecress
for water and nutrients. Interspecific
competition has been noted as
potentially causing reduction in the
extent of the root system in several
small outcrop plant species, thereby
reducing their nutrient uptake (Baskin
and Baskin 1988, p. 836). Shading
further stresses the herbaceous layer,
including the Texas golden gladecress.
In Missouri, stressed glade communities
were more prone to invasion from
invasive species like Schedonorus
phoenix (tall fescue), Sericea lespedeza
(Chinese bushclover), and Rosa
multiflora (multiflora rose) (Hartman
2005, p. 4). On Texas’ Weches glades,
Carr (2005, p. 2) reported tall fescue at
the Chapel Hill site, and Macartney rose
was listed as a major invading species
in pastures throughout the range of
Texas golden gladecress. The Weches
outcrops that parallel SH 21 appear to
support the heaviest Macartney rose
infestation in San Augustine County
(Ritter 2011a, pers. comm.). A 1995
report by the Service’s Clear Lake
Ecological Services Field Office
described known white bladderpod
sites, including several with Texas
golden gladecress, all of which needed
active management to preclude invasion
by woody shrubs (Nemec 1996, p. 1).
Texas golden gladecress habitat has
been documented since the 1980s to be
affected by an accelerated succession
from open, herbaceous Weches outcrops
to dense shrub thickets and closed
canopy woodlands (Service) 1992, p. 7;
Carr 2005, p. 2; Nemec 1996, p. 4). The
most serious invaders are included in
Table 5. Encroachment of these species
is thought to suppress the less
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competitive components of the
community like Texas golden gladecress
and white bladderpod (TNC 2003, p. 4).
Some of these invasive species can grow
on the shallow outcrop soils, while
others can invade open space around
the edges of the outcrop ledges (Service
1992, p. 7). Some of the native invading
species are likely controlled by
occasional wildfire under natural
conditions. More serious are the
introduced invaders, including the
small hop clover that can cover Weches
outcrops and eliminate other vegetation.
56049
The introduced shrubs, including
Macartney rose and Japanese
honeysuckle, will invade open space,
including Texas golden gladecress
habitat (Service 1992, p. 7).
TABLE 5—PRIMARY INVASIVE SPECIES FOUND IN TEXAS GOLDEN GLADECRESS HABITAT
Scientific name
Common name
Nonnative Species
Rosa bracteata .........................................................................................
Lonicera japonica .....................................................................................
Stellaria media ..........................................................................................
Bromus japonicus .....................................................................................
Kummerowia striata ..................................................................................
Ligustrum japonicum ................................................................................
Melilotus indicus .......................................................................................
Cynodon dactylon .....................................................................................
Trifolium dubium .......................................................................................
Macartney rose.
Japanese honeysuckle.
chick-weed.
Japanese brome.
Japanese bush-clover.
Japanese privet.
sour clover.
coastal bermudagrass.
small hop clover.
Native Species
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Andropogon virginicus ..............................................................................
Plantago virginica .....................................................................................
Euphorbia sp ............................................................................................
Frangula caroliniana .................................................................................
Rhamnus lanceolata .................................................................................
Crataegus crus-galli ..................................................................................
Crataegus spathulata ...............................................................................
Prunus mexicana ......................................................................................
Viburnum rufidulum (=prunifolium) ...........................................................
Rhus glabra ..............................................................................................
Ulmus alata ...............................................................................................
Berchemia scandens ................................................................................
Cissus incisa .............................................................................................
The three extant Texas golden
gladecress sites have shrubs and trees
encroaching into formerly open glade
habitat. At the Chapel Hill site, Carr
(2005, p. 2) noted that 13 scattered pines
within a 6,000-ft2 (557-m2) area
produced a total canopy coverage of less
than 10 percent of site, but indicated
that future shading effects when the
pine trees reach maturity might prove
detrimental. At this same site, other
woody plants were controlled, but not
eliminated, by regular shredding (Carr
2005, p. 2).
Texas golden gladecress does show
some ability to persist at sites that have
been overrun by woody vegetation. At
the Geneva site, the area with the Texas
golden gladecress was bulldozed, and
although the site was reported as
destroyed, the species reappeared
within several years. At the Chapel Hill
site, brush removal actions to benefit
white bladderpod also resulted in the
reappearance of the Texas golden
gladecress after its apparent absence for
10 years. This suggests that the Texas
golden gladecress’s seed bank may be
able to remain viable over extended
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broomsedge.
pale-seeded plantain.
spurge.
Carolina buckthorn.
lanceleaf buckthorn.
hawthorn.
hawthorn.
Mexican plum.
rusty blackhaw.
smooth sumac.
winged elm.
Alabama supplejack.
ivy treebine.
time periods even though the habitat is
overgrown by woody species.
Fire suppression is considered a
threat to the continued integrity of the
native plant communities of the Weches
glades because lack of fire contributes to
woody and weedy native and nonnative
plants being able to more quickly
overtake the open glade areas. TNC’s
Area Conservation Plan for the San
Augustine Glades indicated that fire
suppression in the Coastal Plain
Carbonate Glades (another reference for
the Weches glades) constituted a high
level of threat (The Nature Conservancy
2003, p. 9) and that the fire frequency
was ‘‘fair to poor’’; the ideal frequency
being burns occurring every 5 to 10
years. For future viability and
biodiversity health in the glades, the
plan said that fire processes should be
restored or simulated, where feasible
(The Nature Conservancy 2003, p. 8),
and categorized development and
implementation of fire management and
invasive species plans with partner
landowners as a top priority
conservation strategy (The Nature
Conservancy 2003, p. 13). TNC’s plan
also stated that seasonal burns could
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create habitat conditions allowing
establishment and expansion of white
bladderpod populations by triggering
germination and reducing completion
from woody invasives, and referred to
‘‘limited data’’ indicating that burns
conducted July through October (nonbloom period) are the most beneficial
for the bladderpod. This plan also
indicted that this is probably true for the
Texas golden gladecress.
Although information about the direct
effects of prescribed burns on Texas
golden gladecress is not available, Dr.
Michael Warnock did conduct
experimental burns at Caney Creek
Glade Site 6 in the mid-1990s to
determine the impacts on white
bladderpod. His experimental burns did
result in white bladderpod showing a
positive reproductive response.
However, Dr. Warnock did not list the
Texas golden gladecress in his final
report, and did not mention anything
about its response to the experimental
burn (Warnock 1992, entire). The
TXNDD’s element of occurrence records
include descriptions of habitat
conditions, including mention of winter
burns, at a time when the Texas golden
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gladecress was present (in fruit) at two
historic Texas golden gladecress sites.
At Caney Creek Glade Site 2, Texas
golden gladecress was last observed in
March 1988, when the site was
described as being brush-hogged and
burned that same year. In 1988, at the
Caney Creek Glade Site 7, part of the
Weches formation glade area below a
shrubby slope was in part burned that
winter (or early spring), and the Texas
golden gladecress itself was described as
being locally abundant in a very small
area on a seepy, gravelly glade (TXNDD
2012b, pp).
Bermudagrass, ryegrass, and
bahiagrass are nonnative grasses that
have been documented as occurring at
some white bladderpod and Texas
golden gladecress sites. Nemec (1996, p.
4) described bermudagrass as among the
most serious invaders of white
bladderpod and Texas golden gladecress
habitat. Carr (2005, p. 4) listed ryegrass
(although he described it as Lolium
multiflorum (English rye)) as a common
grass component at the Chapel Hill Site
in spring 2005. George (1987, pp. 26–36)
found bermudagrass, bahiagrass, and
perennial ryegrass at San Augustine
County glade sites where he assessed
the herbaceous vegetation community.
Using ‘‘importance values’’ for plant
species that were calculated by
summing the relative density and the
relative frequency of the species (with a
value of 1 being highest or most dense
and most frequent), he found
bermudagrass, ryegrass, and bahiagrass
to rank in importance as 38, 53, and 69
(respectively) of 80 species at site 1;
while ryegrass, bermudagrass, and
bahiagrass ranked as 13, 17, and 23 in
importance (respectively) out of a total
of 75 species at site 2. Interestingly, at
site 3, which was the sole site with
Texas golden gladecress present, only
ryegrass was found; the other two
species were absent. Some of the
differences between the three sites (as
described by George 1987, pp. 26–36)
may have contributed to the presence of
all the invasive grasses at sites 1 and 2,
where they varied with respect to their
frequency and density. Site 3 (where
Texas golden gladecress occurred) was
the rockiest and most fossiliferous of the
three sites, with soil and a gravel-like
substrate containing many small rocks.
Sites 1 and 2 appeared to include more
areas of deeper, more developed soil.
Site 3 was the wettest in the spring and
the driest in the summer and fall, due
to rapid drying of the thin soil. George
(1987, pp. 26–36) postulated that the
thin, rocky soils of Site 3 were probably
a limiting factor that helped to explain
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the generally lower densities of most of
the plants at the site.
George (1987, pp. 26–36) also
described a seasonality component to
the vegetation growth on the Weches
glades. This seasonality may help to
keep the habitat conditions suitable for
the Texas golden gladecress even if
bermudagrass, bahiagrass, and ryegrass
are present. He noted that the spring
was dominated by a sequence of diverse
annual forbs, and as the summer
progressed, rainfall diminished, the soil
dried out, and the flora became very
sparse. The grasses exhibited large
growth spurts in September and
dominated all three sites; however, this
time of grass dominance (summer and
fall months) is the time of year when
Texas golden gladecress is not present
aboveground. Therefore, seasonality of
growth should help to somewhat
ameliorate competition between the
grasses and the annuals on the outcrops.
With regard to ROWs, Texas golden
gladecress does extend into highway
ROWs at several sites. Coastal
bermudagrass and bahiagrass are
included in mixtures used to re-seed
ROWs in the east Texas area (Adams
2013c, pers. comm). Bahiagrass is a
deep-rooted perennial adapted to a wide
range of soils. It spreads via stolons and
rhizomes, in addition to being a prolific
seed producer. Bahiagrass is most
productive on sandy soils with a pH of
5.5 to 6.5 (Houck 2009, p. 1). These
qualities would seem to contraindicate
bahiagrass colonizing and persisting on
the parts of the outcrop where Texas
golden gladecress grows, since
bahiagrass does not share an affinity for
the thin, rocky, or nonexistent soils
under the Texas golden gladecress.
Ryegrasses grow best on fertile, welldrained soils; however, they can also
grow on soils where conditions are too
wet at certain times of the year to
support other grasses because ryegrass is
a heavy water user (Hall 1992, p. 1). Soil
pH for optimum ryegrass production is
between 6.0 and 7.0 (Hall 1992, p. 3), so
it may be able to tolerate the alkalinity
of the Weches outcrops. Perennial
ryegrass requires a dormancy period of
cool temperatures before the
photoperiod can induce flowering, and
it normally produces seed heads during
late spring (Hall 1992, p. 1). This timing
of growth and reproduction may be
offset enough to help to minimize
competition if and when ryegrass does
grow onto Texas golden gladecress
habitat.
Bermudagrass is a vigorous,
stoloniferous grass that can rapidly
invade cultivated land in areas of high
rainfall or irrigation (Duble 2013, p. 1).
Bermudagrass has a fibrous, perennial
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root system with vigorous, deep
rhizomes. Root production and dieback
is reported to be especially high in the
spring when shoot production begins.
Soil temperatures above 65 degrees
Fahrenheit (°F) (18.3 degrees Centigrade
(°C)) are required for significant growth
of rhizomes, roots, and stolons, with the
optimum soil temperature for root
growth around 80 °F (27 °C) (Duble
2013, p. 2). Bermudagrass has the
capability of surviving extreme droughts
and produces seed heads under stress
conditions (Duble 2013, p. 3). This
invasive grass can grow well on a wide
variety of soils from heavy clays to deep
sand, as long as fertility is not limiting.
It can tolerate both acid and alkaline
soil conditions and salinities.
Bermudagrass does not tolerate poorly
drained sites like compacted soils and
heavy clays (Duble 2013, p. 6). Some
qualities of bermudagrass, like its
growth and spread via stolons and shoot
production at nodes, along with its
tolerance of varying pH conditions,
might enhance its ability to invade the
Weches outcrop habitats, and indeed it
has been noted as a significant invader
at some outcrop sites. However, its lack
of tolerance for poor drainage might
preclude it from the portions of the
outcrop favored by the Texas golden
gladecress. Also, its soil temperature
requirements for growing periods may
offset its season of growth and
reproduction from that of the Texas
golden gladecress.
Nonnative and native woody species,
including woody shrubs, vines, and
trees, continue to degrade Texas golden
gladecress’s habitat across the species’
entire range. This threat is significant
for the species because it is ubiquitous
and has led to declines in, or
disappearance of, Texas golden
gladecress populations, along with
altering the species’ habitat. Based on
our review of the scientific and
commercial data available, we conclude
that invasion of woody and weedy
nonnative and native plants into Texas
golden gladecress habitat is a threat
across its range. We recognize the
potential for bermudagrass, bahiagrass,
and ryegrass to impact the habitat of the
Texas golden gladecress, especially in
those situations where these grasses are
deliberately planted nearby to Texas
golden gladecress populations.
However, there are characteristics of
each of the three that may help limit
competition between these nonnative
plants and the Texas golden gladecress,
at least on those Texas golden
gladecress sites that have sufficient
outcrop rock ledge or rock face that
separate the Texas golden gladecress
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from the deeper soils needed by the
grasses. Based on this information, we
do not consider these specific species a
threat at this time. In the future, if these
grasses are shown to impact the Neches
River rose-mallow or Texas golden
gladecress, we will work with the
appropriate agencies and industries to
address these impacts.
Habitat Damage Associated With
Grazing
Grazing has been implicated as a
habitat threat because it can facilitate
the encroachment of undesirable
vegetation into the outcrop habitat, and
because it may lead to trampling of
plants and soil compaction. Historically,
the introduction of grazing livestock
into east Texas, coupled with heavy
grazing pressure, adversely impacted
glade sites by facilitating the spread of
invasive woody plants, and potentially
trampling native plants. Acting in
concert with fire suppression, heavy
grazing pressure may have accelerated
conversion of the grassy prairies and
herbaceous glades to the dense, thorny
masses of vegetation seen at many sites
today (Nemec 1996, p. 4; Service 1992,
p. 7). Overgrazing of Texas golden
gladecress habitat can promote invasion
by woody species and enhance
competition on the glade from
herbaceous weeds like pale-seeded
plantain, Japanese brome, and spurge
(Service 1992, p. 7). Grazing livestock
serve as a source of introduced species’
seeds as well as supplying nutrients for
competitive native weedy species.
Grazing animals can also encourage
unpalatable invasive species like
Macartney rose to move into areas
where more preferred natives have been
grazed out (Bridges 1988, p. II–35). The
negative impacts to Texas golden
gladecress habitat from woody plant
invasion are detailed in the ‘‘Invasive
Species’’ section.
There is no documentation of Texas
golden gladecress plants being lost due
to trampling. Potential does exist for
this to happen, for example, at the
Geneva Site, where Texas golden
gladecress plants have been observed
growing directly adjacent to and inside
the fence where a cow trail is evident.
Loss of plants in this small area has not
been confirmed, and the larger part of
this population grows in the SH 21
ROW, where no grazing takes place, so
it is unlikely that trampling at this site
truly constitutes a threat to the species.
Grazing also occurs within the fenced
private portions of the other two
remaining Texas golden gladecress
population sites (Caney Creek Glade
Site 1 and Chapel Hill), where
individual plants may be subject to
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trampling if they are growing directly in
cattle trails.
Grazing does occur on portions of the
three extant population sites, but we do
not have information to show that
grazing has destroyed Texas golden
gladecress habitat or plants. Based on
our review of the best scientific
information, we conclude that the direct
effects of grazing are not a threat to
Texas golden gladecress.
Land Conversion for Agriculture and
Silviculture
Another potential habitat threat is
conversion of Weches glade outcrops to
nonnative grass pastures or conversion
of existing pasture lands that may
contain viable outcrops to pine tree
plantations. Over the last 200 years,
most of the native vegetation
communities of east Texas were
dramatically altered by human activities
as the region was logged and extensively
cultivated (Diggs et al. 2006, p. 76). Due
to widespread land use changes
throughout the entire range of the Texas
golden gladecress, and the fact that the
glade areas were always somewhat
small and surrounded by forest, there is
a high likelihood that some glades were
negatively affected by past agricultural
and silvicultural land cover conversions
(Service 1992, p. 7). At least one Texas
golden gladecress population was
described as being lost to this type of
land use change during the 1980s
(Turner unpubl. Data, in TNC 2003, p.
2).
Conversion of native vegetation
communities to pasture or row crop in
the region is much less common now.
The Weches outcrops are not considered
desirable substrate for planting to
pasture, as landowners are not
interested in deep plowing, breaking up,
or dragging out rocks (Ritter 2011a, pers.
comm.). The ‘‘Redland’’ soils that are
exposed in the Weches outcrops are thin
and rocky. The Natural Resources
Conservation Service recommends
avoiding these soils because there are
not practical conservation practices for
these types of sites (Ritter 2011a, pers.
comm.). The more prevalent land use
change now is from pasture to tree
plantation (Ritter 2011a, pers. comm.).
Within the last few years, many Sabine
and San Augustine County landowners
have shifted from grazing to timber
planting (Ritter 2011a, pers. comm.).
Most timber planting consists of Pinus
taeda (loblolly pine) and Pinus palustris
(longleaf pine), planted on 8–10 ft (2.4–
3 m) centers. Although landowners will
likely avoid planting directly onto
Weches outcrops because these rocky
soils will not support trees, it is
conceivable that the spacing between
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plantings would allow trees to be
planted near the edges of outcrops
(Ritter 2011a, pers. comm.; Ritter 2012,
pers. comm.). As these trees mature,
their canopies may potentially cause
shading problems on glade areas (see
‘‘Invasive Species’’ section for
explanation of negative effects of
shading). For example, it appears that
former habitat adjacent to the Chapel
Hill site may be planted, in part, to rows
of trees.
In addition to shading, pine tree
plantings may also result in production
of large amounts of pine needle litter
that could accumulate in small glade
openings near the trees. Where a midstory of trees develops, light may be
blocked from reaching the ground level
by upper-canopy and mid-story shading;
with a subsequent build-up of leaf litter,
the herbaceous species can be
suppressed. In the face of fire
suppression, Missouri glades became
choked with litter that kept the ground
moister and cooler, leading to
replacement of the sun-loving natives by
invading cool-season vegetation and
exotic species (Hartman 2005, pp. 2–4).
The decomposition of pine leaf litter
also facilitates the germination of pines
as the soil deepens within the glade
(Walker 2012, pers. comm., p. 1).
Current data do not suggest that the
establishment of pine tree plantations is
a threat to the species. However, if in
close proximity to occupied glade
openings, this may potentially cause
problems for Texas golden gladecress. If
this becomes an issue in the future, we
will consider it in our recovery planning
and implementation.
Herbicide Use
The candidate assessments for Texas
golden gladecress list herbicide use in
highway ROWs and for agricultural
purposes as a potential threat to the
species because of the plant’s
occurrence within highway ROWs and
in pastures. Herbicide use to maintain
highway and county road ROWs has the
potential to destroy the small
subpopulations that exist in the TXDOT
ROWs at the Geneva and Caney Creek
Glade 1 sites. If timing of the herbicide
application coincides with the growing
and reproductive period of the year for
the Texas golden gladecress, all
individuals that are growing in the ROW
might be extirpated if the herbicide
contacts all Texas golden gladecress
individuals in these small sites.
Herbicide exposure from highway and
county road maintenance would affect
only a small portion of two extant sites,
and recent information suggests that use
of herbicides for State and county roads
in this area is not a widespread practice
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(Adams 2011b, pers. comm.; Hunter
2011, pers. comm.). We do not have
documentation of negative impacts to
the species from herbicide applications
for road maintenance. The TXDOT uses
herbicides only on an ‘‘as needed’’ basis
to eliminate encroaching woody plants
or along the edges of the road pavement
(Adams 2011b, pers. comm.). San
Augustine County does not use
herbicides for county roadside
maintenance due to costs (Hunter 2011,
pers. comm.).
With regard to agricultural herbicide
use in San Augustine and Sabine
Counties, the Natural Resources
Conservation Service has a program to
assist landowners with Macartney rose
control using Grazon® P+D herbicide.
This program involves a 3-year
approach—broadcast spraying from a
tractor during the first 2 years, followed
by individual plant treatments in the
third year. Grazon® P+D has active
ingredients of picloram and 2,4-D
(dichlor) and can persist in some soils
for months and act as a preemergent,
killing germinating seedlings. In an
appendix to TNC’s Conservation Area
Plan for the San Augustine Glades (The
Nature Conservancy 2003, pp. 30–31), it
is one of several herbicides identified as
potentially harmful to the Texas golden
gladecress and white bladderpod if used
near their habitats. Management
recommendations include avoiding use
of this herbicide within 200 yards (yd)
(183 m) of areas described as habitat
within the region, along with limiting
timing of use to spot treatments only
between July 1 and August 30. Because
Macartney rose is infesting the region of
the Weches outcrops, and since this
exotic invader is capable of establishing
itself in Weches glades and has been
noted as occurring at Texas golden
gladecress population sites, it is
reasonable to assume that some areas of
glade habitat are included in these
treatment programs. Thus, although
control of Macartney rose would likely
benefit the Texas golden gladecress in
the long term, application of a preemergent herbicide has the potential to
eliminate the Texas golden gladecress
altogether if it stays in the soil long
enough to kill emerging seedlings. We
have no evidence that this type of
application has affected Texas golden
gladecress populations to date.
Based on our review of the scientific
information, we conclude that using
preemergent herbicides such as Grazon®
P+D that persist in the soil for brush
control constitute a threat to Texas
golden gladecress’s emerging seedlings.
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Climate Change
Our analyses under the Act include
consideration of ongoing and projected
changes in climate. The terms ‘‘climate’’
and ‘‘climate change’’ are defined by the
Intergovernmental Panel on Climate
Change. The term ‘‘climate’’ refers to the
mean and variability of different types
of weather conditions over time, with 30
years being a typical period for such
measurements, although shorter or
longer periods also may be used
(Intergovernmental Panel on Climate
Change 2007a, p. 78). The term ‘‘climate
change’’ thus refers to a change in the
mean or variability of one or more
measures of climate (for example,
temperature or precipitation) that
persists for an extended period,
typically decades or longer, whether the
change is due to natural variability,
human activity, or both
(Intergovernmental Panel on Climate
Change 2007a, p. 78).
Scientific measurements spanning
several decades demonstrate that
changes in climate are occurring, and
that the rate of change has been faster
since the 1950s. Examples include
warming of the global climate system,
and substantial increases in
precipitation in some regions of the
world and decreases in other regions.
For these and other examples, see
Intergovernmental Panel on Climate
Change 2007a, p. 30 and Solomon et al.
2007, pp. 35–54, 82–85. Results of
scientific analyses presented by the
Intergovernmental Panel on Climate
Change show that most of the observed
increase in global average temperature
since the mid-20th century cannot be
explained by natural variability in
climate, and is ‘‘very likely’’ (defined by
the Intergovernmental Panel on Climate
Change as 90 percent or higher
probability) due to the observed
increase in greenhouse gas (GHG)
concentrations in the atmosphere as a
result of human activities, particularly
carbon dioxide emissions from use of
fossil fuels (Intergovernmental Panel on
Climate Change 2007a, pp. 5–6 and
figures SPM.3 and SPM.4; Solomon et
al. 2007, pp. 21–35). Further
confirmation of the role of GHGs comes
from analyses by Huber and Knutti
(2011, p. 4), who concluded it is
extremely likely that approximately 75
percent of global warming since 1950
has been caused by human activities.
Scientists use a variety of climate
models, which include consideration of
natural processes and variability, as
well as various scenarios of potential
levels and timing of GHG emissions, to
evaluate the causes of changes already
observed and to project future changes
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in temperature and other climate
conditions (for example, Meehl et al.
2007, entire; Ganguly et al. 2009, pp.
11555, 15558; Prinn et al. 2011, pp. 527,
529). All combinations of models and
emissions scenarios yield very similar
projections of increases in the most
common measure of climate change,
average global surface temperature
(commonly known as global warming),
until about 2030. Although projections
of the magnitude and rate of warming
differ after about 2030, the overall
trajectory of all the projections is one of
increased global warming through the
end of this century, even for the
projections based on scenarios that
assume that GHG emissions will
stabilize or decline. Thus, there is strong
scientific support for projections that
warming will continue through the 21st
century, and that the magnitude and
rate of change will be influenced
substantially by the extent of GHG
emissions (Intergovernmental Panel on
Climate Change 2007a, pp. 44–45;
Meehl et al. 2007, pp. 760–764, 797–
811; Ganguly et al. 2009, pp. 15555–
15558; Prinn et al. 2011, pp. 527, 529).
(See IPCC 2007b, p. 8, for a summary of
other global projections of climaterelated changes, such as frequency of
heat waves and changes in
precipitation. Also see
Intergovernmental Panel on Climate
Change 2011 (entire) for a summary of
observations and projections of extreme
climate events.)
Various changes in climate may have
direct or indirect effects on species.
These effects may be positive, neutral,
or negative, and they may change over
time, depending on the species and
other relevant considerations, such as
interactions of climate with other
variables (for example, habitat
fragmentation) (Intergovernmental Panel
on Climate Change 2007a, pp. 8–14, 18–
19). Identifying likely effects often
involves aspects of climate change
vulnerability analysis. Vulnerability
refers to the degree to which a species
(or system) is susceptible to, and unable
to cope with, adverse effects of climate
change, including climate variability
and extremes. Vulnerability is a
function of the type, magnitude, and
rate of climate change and variation to
which a species is exposed, its
sensitivity, and its adaptive capacity
(Intergovernmental Panel on Climate
Change 2007a, p. 89; Glick et al. 2011,
pp. 19–22). There is no single method
for conducting such analyses that
applies to all situations (Glick et al.
2011, p. 3). We use our expert judgment
and appropriate analytical approaches
to weigh relevant information, including
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uncertainty, in our consideration of
various aspects of climate change.
As is the case with all stressors that
we assess, even if we conclude that a
species is currently affected or is likely
to be affected in a negative way by one
or more climate-related impacts, it does
not necessarily follow that the species
meets the definition of an ‘‘endangered
species’’ or a ‘‘threatened species’’
under the Act. If a species is listed as
endangered or threatened, knowledge
regarding the vulnerability of the
species to, and known or anticipated
impacts from, climate-associated
changes in environmental conditions
can be used to help devise appropriate
strategies for its recovery.
The climate in Texas has shown a
long-term gradual warming trend;
pollen, plant macrofossils (fossils large
enough to be seen without a
microscope), packrat middens (ancient
‘‘garbage piles’’ left by rodents in the
genus Neotoma), and other evidence
show substantial climate changes in
Texas over the past 15,000 years (end of
the last glacial period), when the mean
annual air temperature was 9 °F (5 °C)
cooler than present (Diggs et al. 2006, p.
73). The Texas climate is considered
highly variable, with seasonal
precipitation patterns that dramatically
increase from west to east, and
temperatures that increase from north to
south (Nielsen-Gammon 2008, p.1).
Climate models predict increased
temperatures, and concurrent increased
evapotranspiration, and decreased
regular precipitation and soil moisture
in Texas (Diggs et al. 2006, p. 73), all of
which would have negative
implications for Texas golden
gladecress. Based on a climate model
developed by the United Kingdom
Hadley Center (HadCM2), temperatures
in Texas could increase by 3 °F (1.7 °C)
in spring (range of 1–6 °F (0.6–3.3 °C))
and about 4 °F (2.2 °C) in other seasons
(with range of 1–9 °F (0.6–5 °C)).
Droughts are not uncommon in Texas
(Texas Water Resources Institute 2011,
pp. 1–13). The most severe drought
recorded in Texas occurred in the
1950s, and in the last 15 years there
have been widespread droughts: in
1996, 1999–2000, 2005–2006, 2007, and
2010–2011 (Texas Water Resources
Institute 2011, pp. 10–12). Projections
are for winter precipitation to decrease
by 5 to 30 percent, although it may
increase by 10 percent in other seasons
(Environmental Protection Agency 1997,
p. 2).
East Texas is subtropical with a wide
range of extremes in weather (Diggs et
al 2006, p. 65). Mean annual
temperatures range from 70 °F (21 °C) in
the south to approximately 64 °F (18 °C)
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in the north, although extremes like 0 °F
(¥18 °C) and 110 °F (43 °C) are
observed occasionally. The highest
reported eastern Texas temperature was
118 °F (48 °C) in Collin County in 1936
(Bomar 1995, in Diggs et al. 2006, p. 65).
Average rainfall ranges from 60 in (152
cm) at the State’s southeastern border to
40 in (98 cm) at the western edge. These
rainfall differences are related to
proximity to the warm, moist air
supplied by the Gulf of Mexico. The
native vegetation of this region evolved
with, and is adapted to, recurrent
extremes (Diggs et al. 2006, p. 67). That
said, the Pineywoods region is
vulnerable to even small climatic shifts
because it is ‘‘balanced’’ on the eastern
edge of a dramatic precipitation
gradient. Temperature increases that are
projected in climate change scenarios
will likely be associated with increases
in transpiration and more frequent
summer droughts. Decreased rainfall
may result in an eastward shift in the
forest boundary and replacement of the
Pineywoods forest with scrubland
(Diggs et al. 2006, p. 80). There is
potential for loss of species that are
limited to mesic conditions of deep east
Texas, such as the hardwood forests
surrounding the Weches glades. There
may also be a northerly shift of
southerly species based on climate
models that predict increasing
temperatures and, therefore, increasing
evapotranspiration and decreasing
regional precipitation and soil moisture
(Diggs et al. 2006, p. 73).
Although east Texas has typically
received a greater amount of
precipitation during December through
March than other regions (NeilsenGammon, p. 24), future precipitation
trends indicate a decrease in
precipitation toward the middle of the
21st century (Nielsen-Gammon, p. 28).
The timing of this precipitation is
crucial for the Texas golden gladecress,
which is dependent on late-fall-throughspring moisture to generate the seeps
and pooling that it requires for
germination, growth, and reproduction.
Reproduction is known to be negatively
impacted by drought as evidenced by
declines of 91 to 67 plants at the Chapel
Hill site and 490 to 96 plants at the
Caney Creek Glade Site 1 during the
1999–2000 droughts (Service 2010b, p.
5; Singhurst 2011a, pers. comm.). It is
unknown how the Texas golden
gladecress will respond to continued
years of drought, especially when
combined with other threats. Godwin
(2012, pers. comm., p. 4) noted that
droughts have had a major effect on the
distribution of biota in east Texas and
hypothesized that drought has
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contributed to isolation and endemism
in the glade flora.
A warmer climate with more frequent
droughts, but also extreme precipitation
events, may adversely affect Texas
golden gladecress by altering the glade
habitat the species is known to occupy.
It may improve habitat conditions for
invasive plant species and other plants
(Service 2010b, p. 5), although,
conversely, extreme drought years may
contribute to keeping woody species
from overtaking glades by making the
shallow soil even more inhospitable to
larger plants. Godwin (2012, pers.
comm., p. 1) personally observed the
drought of 2011 ‘‘pushing back’’ the
edges of Weches glades and tiny saline
prairies. Climate extremes, especially
drought and low temperatures, probably
play a bigger role in excluding
nonadapted species than average
conditions will (Diggs et al. 2006, p. 80).
Because the Texas golden gladecress is
a habitat specialist, being closely tied to
the geology and soils on the Weches
outcrops, it seems unlikely that this
species will be flexible in terms of
shifting to new habitats if the glades
become unsuitable due to lack of
winter-spring moisture. Also, if
conditions shift in favor of nonnative
plants, the Texas golden gladecress will
likely be negatively affected. Although
the Texas golden gladecress has
survived cycles of drought in the past,
as well as some years with extraordinary
temperature shifts, it may have done so
in a landscape where it was more
abundant and with populations
distributed in closer proximity to one
another. Based on our review, the best
scientific and commercial data available
did not provide us with information
regarding the species’ seedbank, so we
do not know how many consecutive
years of poor conditions (in terms of low
rainfall and high temperatures) the
species can survive.
The best scientific and commercial
data available do not provide reliable
predictions for future patterns of
precipitation and temperature that are
specific to east Texas. While it appears
reasonable to assume that climate
change will occur within the range of
Texas golden gladecress, at this time we
do not have information to indicate
specifically how climate change may
affect the species, its habitat, or
responses of invasive species in these
habitats.
Other Conservation Efforts
Habitat conditions conducive to the
Texas golden gladecress’s persistence
are being maintained at the Chapel Hill
population site by the landowner. Texas
golden gladecress was an incidental
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beneficiary of a brush removal project
done for white bladderpod at this site in
1995, when the private landowner,
working in cooperation with the
Service, cleared shrubby overgrowth
from his small tract of land. As a result
of this glade being reopened, the Texas
golden gladecress reappeared after a 10year absence (Nemec 1996, p. 5). This
success demonstrated that removal of
woody and weedy invaders may help
the Texas golden gladecress seedbed to
germinate and the plant to emerge.
Because this site experienced rapid
reinvasion of shrubs, repeated
maintenance was required to keep the
site open, and the landowner has
voluntarily continued to mow or
bushhog at least once per year
(Singhurst 2012f, pers. comm.). As a
result, the Texas golden gladecress and
bladderpod were still seen to occupy
this site as recently as February 2012
(Singhurst 2012f, pers. comm.).
Within the past several years, the
Service’s Partners for Fish and Wildlife
Program has funded a habitat restoration
project involving brush clearing and
planting of white bladderpod in a glade
at a privately owned tract in San
Augustine County. It was also hoped
that Texas golden gladecress would
benefit from this project, but the species
has not been detected at the site to date.
A past conservation effort proved that
there is some potential to reintroduce or
create new populations of Texas golden
gladecress. The species was successfully
introduced via seed into apparently
appropriate habitat in Nacogdoches
County at a site located approximately
30 mi (48 km) west of its historic range
in the late 1980s, where it continued to
grow until 2011, when a pipeline
excavation eliminated the population.
The success of this introduction effort
was a positive indication of possibilities
to augment existing population sites or
introduce Texas golden gladecress into
other currently unoccupied but suitable
habitat sites to form new populations.
In addition to habitat projects, the
Service funded several projects with
TNC, including one that provided for 3
years of status surveys for Texas golden
gladecress and white bladderpod. These
surveys, completed in 2006, were the
sole source of population numbers for
these species for several years. TNC also
attempted to identify appropriate glade
habitats in which Texas golden
gladecress and white bladderpod might
be found using GIS data (aerial, geology,
and hydrology sources) (Turner 2000
pers. comm.), but follow-up site visits
showed little Weches habitat and no
new Texas golden gladecress
populations at what appeared to be
suitable sites (Turner 2003, p. 4, in
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Service 2010a). In 2001, TNC collected
Texas golden gladecress seeds from four
sites for cultivation, research, and longterm storage, and as seed sources for
reintroduction work. The seeds were
given to Mercer Arboretum, where they
have been in long-term storage, as well
as being used for some early
germination and cultivation work. The
species was successfully introduced
into apparently appropriate habitat in
Nacogdoches County at a site located
approximately 30 mi (48 km) west of its
historic range in the late 1980s, where
it grew and reproduced through 2011,
when it was eradicated by construction
of a pipeline. The success of this
reintroduction project may bode well for
future efforts to increase the numbers of
populations by reintroductions or
introductions to new sites.
Summary of Factor A
The threat that has the most
significant impacts to Texas golden
gladecres populations is the loss and
degradation of habitat. Specifically,
surface quarrying of glauconite and the
exploration and development of oil and
natural gas wells and associated roads
and pipelines have destroyed 50 percent
of the known populations between the
mid-1990s and 2011. The threats from
quarry development are likely to
continue, as glauconite is currently in
demand for road bed and well pad
construction, as well as for use in
fertilizer and as an animal feed additive.
For the past several years, energy
exploration and production, especially
natural gas, has been active due to
development of the natural-gas-bearing
Haynesville Shale, which underlies the
entire range of Texas golden gladecress.
For the four remaining populations,
these activities pose ongoing threats
because we cannot predict whether new
pipelines, well pads, roads, or quarries
are planned for the areas where the
populations occur. The populations of
Texas golden gladecress are found
mainly on privately owned land where
no level of protection for the plants is
guaranteed. Portions of two extant
populations extend into SH ROWs
where TXDOT has the ability to provide
some protections but only for those few
plants that are on the ROW. Much of the
species’ potential habitat throughout its
range occurs on private lands that have
not been surveyed; therefore, the current
level of threats across these lands
cannot be assessed. The excavation
activities associated with surface
quarrying of glauconite and oil and gas
development are threats that have
significant impacts to the known extant
populations and associated habitats of
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the gladecress, both now and in the
future.
We have also determined that the
damage to Texas golden gladecress
plants and outcrop habitat that is
associated with excavations may occur
when pipelines for water, sewer lines,
gas connections to homes, and
communication lines are installed. New
power lines that are built outside of
established ROWs also have potential to
damage Texas golden gladecress
populations and habitat if land-clearing
activity and heavy equipment directly
cross occupied outcrops. Although we
acknowledge that these activities
constitute potential threats to the
species and its habitat, we do not know
where service improvements are
planned within the range of the species
or the number of these types of projects
that are planned for the future.
Texas golden gladecress also faces
threats throughout its range from
competition for light and nutrients from
both native and nonnative, invasive,
woody plants, including the nonnative
Macartney rose. We have determined
that the extant populations will decline
or become extirpated unless they are
periodically maintained to remove
invading trees and shrubs. Additionally,
herbicides used to control Macartney
rose may be a threat to the Texas golden
gladecress if applied to or persisting in
the soil during the species’ period of
growth, from late fall through early
summer.
A recent, ongoing trend in local land
use is the conversion of open pasture to
pine plantations. However, densely
planted pine trees may degrade the
species’ habitat due to competition for
light and nutrients and by contributing
masses of leaf litter onto formerly
sparsely vegetated glades.
Finally, the information regarding
climate change is not yet specific
enough for us to determine the potential
long-term effects to the Texas golden
gladecress’s habitat. However, long-term
drought has negatively affected and will
likely continue to negatively affect the
reproduction and germination of Texas
golden gladecress seeds.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Limited collection of Texas golden
gladecress has occurred for scientific
purposes; only voucher specimens and
several seed collection events are
documented. Dr. Elray Nixon collected
seed in 1987, and successfully created a
new population when he introduced the
seed onto an outcrop in Nacogdoches
County. TNC collected seed at four sites
in 2001, and contributed these seed
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collections to Mercer Arboretum, a
participating institution in the Center
for Plant Conservation, in 2002 (Tiller
2013, pers. comm., p. 1). Mercer
maintained some in long-term storage
and planted some in germination trials.
There are no records of any collections
of seeds or other plant materials in the
last few years. Because these collections
were limited, we do not believe that this
activity constitutes a threat to the
species. There is no information to
suggest that Texas golden gladecress is
collected for commercial, recreational,
or educational purposes, and we have
no reason to believe that this factor will
become a threat to the species in the
future. Therefore, based on our review
of the best available scientific and
commercial information, we conclude
that collection or overutilization of
Texas golden gladecress is not currently
a threat to the species, nor do we expect
it to become a threat in the future.
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C. Disease or Predation
Our review of the best available
scientific and commercial information
regarding disease in Texas golden
gladecress does not indicate that disease
or predation are issues for this species.
There is no information regarding
predation by wildlife on the species.
Grazing is ongoing across the range of
the Texas golden gladecress and occurs
on portions of all extant population
sites; however, there is no information
to document that cattle eat Texas golden
gladecress. No studies have been
conducted to investigate the effect of
grazing or herbivory specifically on
Texas golden gladecress. George (1987,
p. 17) studied the herbaceous flora of
three Weches outcrops in San Augustine
County and saw little grazing within his
study plots although cattle were present
at all three sites. Therefore, based on our
review of the best available scientific
and commercial information, we
conclude that disease and predation on
Texas golden gladecress, including
predation associated with grazing, are
not currently threats to the species, nor
do we expect disease or predation to
become a threat in the future.
D. The Inadequacy of Existing
Regulatory Mechanisms
Under this factor, we examine
whether existing regulatory mechanisms
are inadequate to address the threats to
the species discussed under the other
factors. Section 4(b)(1)(A) of the Act
requires the Service to take into account
‘‘those efforts, if any, being made by any
State or foreign nation, or any political
subdivision of a State or foreign nation,
to protect such species. . .’’. In relation
to Factor D under the Act, we interpret
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this language to require the Service to
consider relevant Federal, State, and
tribal laws, regulations, and other such
mechanisms that may minimize any of
the threats we describe in threat
analyses under the other four factors, or
otherwise enhance conservation of the
species. We give strongest weight to
statutes and their implementing
regulations and to management
direction that stems from those laws and
regulations. An example would be State
governmental actions enforced under a
State statute or constitution, or Federal
action under statute.
Having evaluated the significance of
the threat as mitigated by any such
conservation efforts, we analyze under
Factor D the extent to which existing
regulatory mechanisms are inadequate
to address the specific threats to the
species. Regulatory mechanisms, if they
exist, may reduce or eliminate the
impacts from one or more identified
threats. In this section, we review
existing State and Federal regulatory
mechanisms to determine whether they
effectively reduce or remove threats to
the Texas golden gladecress.
The greatest threats to the Texas
golden gladecress include loss of habitat
and the plants themselves due to actions
that remove the substrate under the
populations or that cover them up.
These types of actions have been
associated with quarrying of glauconite;
construction related to natural gas and
oil exploration and production;
conversion of native glades or pastures
with glades and outcrops to other land
uses, most recently planting to pine
plantations; installation of service lines;
and potentially herbicide applications
for purposes of controlling the invasive
Macartney rose.
Existing State and Federal regulations
that might help conserve rare species on
SH ROWs, including avoidance or
minimization of habitat destruction, as
well as regulations that would protect
plants from herbicide applications, are
requirements only for already listed
species; therefore, these regulations do
not apply to Texas golden gladecress. Of
the two Texas golden gladecress
populations that occur in ROWs, the
federally listed white bladderpod is
only found at one site (Caney Creek
Glade Site 1). Although the Texas
golden gladecress plants at the Caney
Creek Glade Site 1 do extend into the
TXDOT-maintained ROW, the majority
of the plants are on the adjacent private
land, so any protections offered by the
State would apply to very few of the
plants. Likewise, no existing regulations
protect the species on privately owned
land, where most of the remnant Texas
golden gladecress is found.
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Currently, Texas golden gladecress is
not protected by State or Federal laws.
All of the populations occur on private
property even though portions of those
populations extend onto SH ROWs; the
ROW portions of these populations are
miniscule. As such, the existing
regulatory mechanisms are inadequate
to address the threats to the species.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Small Population Size
The Texas golden gladecress remains
in only three small populations. Small
populations can be prone to extirpation,
especially if a series of drought years
greatly reduces seed production and
depletes the soil seed bank. The Service
(1992, p. 8) noted that for a species like
the white bladderpod, with only small
populations and wide natural annual
fluctuations in plant numbers, as well as
fragmented habitat across its range,
recolonization after a population loss
would require long-distance seed
dispersal. Although we have no
information regarding the Texas golden
gladecress’s seed dispersal patterns or
distances, we do know that the Texas
golden gladecress’s habitat is
exceedingly fragmented, with fewer and
smaller known populations than the
bladderpod, and farther distances
between populations. This makes the
prospects for recolonization after a
potential loss of a Texas golden
gladecress population very remote.
Small populations can also be prone
to extirpation from a single adverse
natural or manmade event. The
population at the Chapel Hill site is a
good example of this vulnerability. Carr
(2005, p. 2) reported that Texas golden
gladecress habitat was extremely limited
at Chapel Hill and that the numbers of
Texas golden gladecress plants would
also always be restricted by the small
size of the available habitat. He
concluded that the population was so
small that a single adverse event could
extirpate the species from this location.
The small population size and the small
number of extant populations of Texas
golden gladecress increases each
population’s vulnerability to the threats
that have significant impacts described
under Factor A. Low numbers of plants,
confined to very small areas, can be
totally eradicated by actions such as
installation of pipelines; excavation of
mines; or construction of well pads,
roads, or other types of construction.
The remaining Texas golden gladecress
occurrences are so small that they can
fall completely within the footprint of
one well pad, or even within the width
of a pipeline excavation. Small
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population size also increases the risk of
total loss of populations due to contact
with herbicides or shading and leaf
litter accumulation from pine tree
plantings because these threats are
likely to affect the entirety of any given
occurrence. Sustained drought may
reduce the reproductive effort of a
population, and this can lead to an
overall decrease in fitness for the
remaining populations. Reduced
reproductive effort affects the seed bank,
which represents the reproductive
capacity of each Texas golden
gladecress population. The combined
effects of drought, impacts from oil and
gas development, herbicide treatment,
shading, and competition place the
remaining three populations at a high
risk of extinction, exacerbated by their
small population size and narrow
distribution.
In addition to increasing vulnerability
to direct threats such as pipeline
construction, small population size can
result in a decrease in genetic diversity
due to genetic drift (the random change
in genetic variation in each generation)
and inbreeding (mating of related
individuals) (Antonovics 1976, p. 238;
Ellstram and Elam 1993, pp. 218–219).
Genetic drift can decrease genetic
variation within a population by
favoring certain characteristics and,
thereby, increasing differences between
populations (Ellstram and Elam 1993,
pp. 218–219). This increased difference
between populations can diminish a
species’ ability to adapt to the selective
pressures of a changing environment
(Newman and Pilson 1997, p. 360;
Ellstrand 1992, p. 77). Self-fertilization
and low dispersal rates can cause low
genetic diversity due to inbreeding
(Antonovics 1976, p. 238; Barrett and
Kohn 1991, p. 21).
Although we do know that Texas
golden gladecress exists in small
populations in a fragmented landscape,
we do not know whether these
remaining populations are peripheral to
what may have been a historically larger
range. Although we might infer
inbreeding is occurring in gladecress
based on the species’ isolated
occurrences and ability to self-fertilize,
the best scientific and commercial data
available do not describe genetic
diversity exhibited by the species.
Summary of Factor E
Texas golden gladecress is a
historically rare species with some
adaptations, such as a mixed mating
system, that help to alleviate part of the
inherent risks of small population size.
The continued existence of Texas
golden gladecress is negatively
impacted by natural factors including
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being limited to only a few remaining
populations that contain very small
numbers of individual plants with a
distribution restricted to extremely
small areas of outcrop. The species’
current, reduced occurrences across a
range that has been highly fragmented
by past and ongoing human activities
increase its vulnerability. With only
three remaining populations, loss of an
entire population could be catastrophic
for this species’ long-term viability.
Therefore, based on our review of the
best available scientific and commercial
information, we conclude that the small
number of remaining populations, all of
which are small in size, in conjunction
with the threats described under Factor
A, constitutes a threat to the species and
greatly exacerbates other the threats we
identify above for this species.
Conservation Efforts To Reduce Other
Natural or Manmade Factors Affecting
Its Continued Existence
We have several examples of
voluntary conservation efforts that are
currently underway, or which took
place in the past, that directly, or
indirectly, assist the Texas golden
gladecress by addressing the impacts of
habitat loss and degradation, or low
population and individual plant
numbers. See description under the
Factor A analysis, above.
Cumulative Effects From Factors A
Through E
As described above under Factor E,
Texas golden gladecress’s small
population size and the small number of
extant populations increase each
population’s vulnerability to the
significant threats described under
Factor A. Small numbers of plants,
confined to very small areas, can be
extirpated by actions such as
installation of pipelines; excavation of
mines; or construction of well pads,
roads, or other types of construction.
The remaining Texas golden gladecress
populations are so small that they can
fall completely within the footprint of
one well pad, or even within the width
of a pipeline excavation. This has been
the case for four of the eight Texas
golden gladecress populations ever
documented; three of these were
extirpated due to quarry excavation
between the late 1980s and the mid1990s. The continued threat of
extirpation of populations to excavation
projects continues, as evidenced by the
loss of the fourth population (the
introduced population) to a pipeline
installation as recently as 2011.
Small population size also increases
the risk of total loss of populations due
to contact with herbicides or shading
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and leaf litter accumulation from pine
tree plantings because these threats are
likely to affect the entirety of any given
occurrence. The high incidence of
Macartney rose invasion within the
Texas golden gladecress’s range could
increase the species’ likelihood of
exposure to herbicides associated with
Macartney rose-control projects.
The overgrowth of many glade
habitats by woody shrubs, particularly
Macartney rose and Chinese privet,
within the range of Texas golden
gladecress also puts these few small
populations at an increased risk of
genetic isolation if the plant is forced
into dormancy by hostile conditions on
the glade. Sustained drought could also
reduce the reproductive effort of a
population, and this can lead to an
overall decrease in fitness for the
remaining populations. Reduced
reproductive effort affects the seed bank,
which represents the reproductive
capacity of each Texas golden
gladecress population.
The combined effects of drought,
impacts from oil and gas development
or other excavations, herbicide
treatment, shading, and competition
place the remaining three populations at
a high extinction risk, and this is
exacerbated by their small population
size and very restricted geographic
distribution.
Determination
Standard for Review
Section 4 of the Act, and its
implementing regulations at 50 CFR part
424, set forth the procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. Under section 4(b)(1)(A), the
Secretary is to make endangered or
threatened determinations required by
subsection 4(a)(1) solely on the basis of
the best scientific and commercial data
available to her after conducting a
review of the status of the species and
after taking into account conservation
efforts by States or foreign nations. The
standards for determining whether a
species is endangered or threatened are
provided in section 3 of the Act. An
endangered species is any species that
is ‘‘in danger of extinction throughout
all or a significant portion of its range.’’
A threatened species is any species that
is ‘‘likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.’’ Per section 4(a)(1) of the Act,
in reviewing the status of the species to
determine if it meets the definition of
endangered or threatened, we determine
whether any species is an endangered
species or a threatened species because
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of any of the following five factors: (A)
The present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; and (E)
other natural or manmade factors
affecting its continued existence.
Listing Status Determination
Based on our review of the best
available scientific and commercial
data, we conclude that the Texas golden
gladecress is currently in danger of
extinction throughout all of its range
and, therefore, meets the definition of
an endangered species. This finding,
explained below, is based on our
conclusions that the severity of threats
is high and occurs throughout the range
of the species. The Texas golden
gladecress has demonstrated some
ability to survive certain events (dozing
and drought) likely due to persistent
seed bank and some ability to tolerate
small population sizes likely due to selffertilization. However, it shows little to
no ability to survive or tolerate other
impacts (quarry mining and pipelines).
Further, although somewhat able to
persist in the face of past naturally
occurring stochastic events, the species
is currently highly vulnerable due to the
limited distribution of populations
across its range and to the specific
habitat requirements needed to support
the species. We find that the Texas
golden gladecress is at an elevated risk
of extinction now, and there is no
information to suggest that the species’
status will improve without significant
conservation intervention. We,
therefore, find that the Texas golden
gladecress meets the definition of an
endangered species under the Act.
On the basis of our biological review
documented in this final rule to list the
Texas golden gladecress, we find the
species is vulnerable to population
extirpations due to its specialized
habitat requirements; restricted
geographic distribution; moisture
regime requirements; small, isolated
populations; and few remaining
populations (Factors A and E). The
species is endemic to Weches glade
habitat, which is scattered or patchy
across the landscape. Its historic range
does not extend farther than
approximately 12 miles (19 km) from
the most southeastern to the most
northwestern documented locations,
and all occurrences were located within
a 3.1-mile-wide (5-km-wide) band
around SH 21. The extant populations
exhibit a high degree of isolation, being
separated from each other by distances
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of 4.5 mi (7.2 km) and 7 mi (11.3 km),
respectively, between the northern
(Caney Creek Glade Site 1), central
(Chapel Hill), and southern (Geneva)
populations. All three extant
populations are small in terms of areal
extent and number of individual plants.
The remaining three sites cover less
than 1.2 ac (0.5 ha). The loss of any of
the known populations further reduces
the ability of the species as a whole to
withstand additional threats.
The remaining small, isolated Texas
golden gladecress populations are
particularly susceptible to extirpation
from habitat loss and degradation
(Factor A). The main sources of habitat
loss and degradation include
construction of glauconite mines,
construction of pipelines, and invasive
woody plants. Glauconite mines and
pipelines remove the habitat and the
overlying Texas golden gladecress
plants, which eliminates the entire
glade or alters hydrology of glades
nearby; allow the invasion of the open,
sunny glade habitats by native and
nonnative woody and weedy species;
and can prompt the planting of pine
trees in close proximity to occupied
glades, which reduces sunlight and
increases leaf litter. Drought decreases
seed production. Successive years of
drought could lead to further declines in
the numbers of plants, or perhaps total
loss of Texas golden gladecress
populations, if no growth or
reproduction occurs over this extended
time period, a circumstance that could
be exacerbated by climate change.
In addition to the individual sources
of habitat loss and degradation under
Factor A, and small, isolated
populations under Factor E, the
cumulative effects of the multiple
stressors are acting on populations such
that the effects on the Texas golden
gladecress, as well as the immediacy of
these threats, are significant throughout
the species’ entire current range. The
small and limited number of remaining
populations act in concert with the
threats under Factor A and E. These
factors pose imminent threats to the
species because they are ongoing. The
current conditions of small and isolated
populations reduce the ability of any
given Texas golden gladecress
population to endure such adverse
events, and natural recolonization
following local extirpations is
considered unlikely in most cases.
We evaluated whether the Texas
golden gladecress is in danger of
extinction now (i.e., an endangered
species) or is likely to become in danger
of extinction in the foreseeable future
(i.e., a threatened species). The
foreseeable future refers to the extent to
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which the Secretary of the Interior can
reasonably rely on predictions about the
future in making determinations about
the future conservation status of the
species. A key statutory difference
between an endangered species and a
threatened species is the timing of when
a species may be in danger of extinction
either now (endangered species) or in
the foreseeable future (threatened
species).
Because of the fact-specific nature of
listing determinations, there is no single
metric for determining if a species is ‘‘in
danger of extinction’’ now. In the case
of the Texas golden gladecress, the best
available information indicates that,
while a major range reduction (that is
the overall geographic extent of the
species’ occurrences) has not happened,
habitat destruction has resulted in
significant loss of populations and
reductions in total numbers of
individuals. These losses are ongoing, as
at least one population was lost due to
a pipeline installation within the last 3
years and three populations were lost
between 1994 and 2011 due to quarry
mining. Because the types of human
activities that have contributed to the
losses of Texas golden gladecress
populations are continuing to occur
across the species’ range, we anticipate
that future losses of the remaining
populations are likely to occur.
Additionally, degradation of the species’
habitat across its entire range is
continuing as woody and weedy plants
overrun glade sites. Further, an increase
in the number and duration of drought
events is projected to continue. Without
substantial conservation efforts, this
trend of population loss is expected to
continue and result in an elevated risk
of extinction of the species. The narrow
endemism of the species, with its small
geographic range, increases the risk for
the species that stochastic events (e.g.,
drought) will affect all known extant
populations, putting the Texas golden
gladecress at a high risk of extinction.
Under the Act and our implementing
regulations, a species may warrant
listing if it is endangered or threatened
throughout all or a significant portion of
its range. The threats to the survival of
this species occur throughout its range
and are not restricted to any particular
significant portion of its range.
Accordingly, our assessments and
determinations apply to this species
throughout its entire range.
In conclusion, as described above, the
Texas golden gladecress has
experienced significant reductions in
population numbers (based on habitat
loss and degradation). The Texas golden
gladecress is especially vulnerable to
impacts due to its life history and
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ecology. The species is also subject to
significant current and ongoing threats.
After a review of the best available
scientific information as it relates to the
status of the species and the five listing
factors, we find the Texas golden
gladecress is in danger of extinction
now. Therefore, on the basis of the best
available scientific and commercial
information, we are listing the Texas
golden gladecress as an endangered
species, in accordance with section 3(6)
of the Act. We find that a threatened
species status is not appropriate for the
Texas golden gladecress because the
threats to the species are occurring now
and are expected to continue into the
future such that overall risk of
extinction is high at this time.
Neches River Rose-mallow
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Neches River rose-mallow is a
nonwoody, flowering perennial found
within seasonally or regularly
inundated sloughs, oxbows, terraces,
sand bars, and bottomlands. The Neches
River rose-mallow is endemic to
relatively open habitat with hydric
alluvial soils (water-saturated soils).
Sites are found within the Neches,
Sabine, and Angelina River basins and
the Mud and Tantabogue Creek basins
of five counties within east Texas.
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Nonnative Species
Nonnative plant species are a constant
threat to native flora throughout the
Gulf coast prairies of Texas and
Louisiana (McCormick 2005, p. 23). A
primary threat to the Neches River rosemallow is the ongoing encroachment of
nonnative and native woody species
into its generally open, intermittent or
perennial wetlands. We considered the
potential threat from three nonnative
species, Chinese tallow, coastal
bermudagrass, and bahiagrass (Miller
2011, pers. comm.). Based on the best
scientific and commercial data
available, the Chinese tallow is an
ongoing threat to the Neches River rosemallow, but coastal bermudagrass and
bahiagrass are not threats at this time.
Chinese tallow was introduced to the
United States in the 1700s from China
(McCormick 2005, pp. 7, 8). With the
ability to reproduce quickly, reach
reproductive maturity in as little as 3
years, and remain reproductively
mature for at least 60 years (United
States Geological Survey (USGS), 2000,
p. 2) to 100 years (Gan et al. 2009, p.
1346), Chinese tallow can produce an
abundance of seed annually (Potts 1946,
p. 375; Conway et al. 2000, pp. 268–
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269). Chinese tallow tolerates a range of
habitat conditions, including full
sunlight and shade, and both flooding
and drought-stricken habitats (USGS
2000, p. 1). These features allow
Chinese tallow to dominate certain
habitats. Butterfield et al. (2004, p. 338)
also found that Chinese tallow grew
faster than native species found within
the Neches River rose-mallow habitat,
such as loblolly pine, water tupelo
(Nyssa aquatica), blackgum (N.
sylvatica), and sweetgum, which occur
in both perennially and intermittently
wet habitats. Without management, the
Chinese tallow has the ability to shade
out, out-grow, and limit water and
nutrient absorption to Neches River
rose-mallow and its native vegetative
associated species.
While there are methods to control
Chinese tallow, these methods are labor
intensive, expensive, and limited in
their effectiveness. Burning,
mechanical, and chemical (herbicide)
means can be used to control Chinese
tallow; however, prescribed fire has
produced complex and highly variable
results in Chinese tallow and may not
be an effective management tool (Grace
1998, entire; Grace 2011, pers. comm.).
The Davy Crockett NF is establishing a
regular burn cycle of 3–4 years for all
compartments containing the Neches
River rose-mallow to control Chinese
tallow and to mimic the historical fire
regimes of the Coastal Plain (Landers et
al. 1990, p. 136). The Davy Crockett NF
Revised Land and Resource
Management Plan for National Forests
and Grasslands in Texas (specific to the
streamside Management Area 4 where
the Neches rose-mallow occurs) allows
for mechanical means and prescribed
fire to maintain the native plant
community but prohibits the use of
chemical agents (herbicides) unless
applied by hand or through nonaqueous
form within 100 feet (30.5 m) of the
Neches River rose-mallow (United
States Department of Agriculture 1996,
p. 154). Despite the available
management actions, Chinese tallow
remains at all USFS sites. Current
mowing activities along ROWs may
abate some growth of Chinese tallow,
but management actions on these sites
should also be evaluated for their
effectiveness. Chemical methods are not
being used to control Chinese tallow.
The invasion from nonnative Chinese
tallow tree has historically been a threat
to the Neches River rose-mallow and
continues to be a threat. Chinese tallow
occurs at all Neches River rose-mallow
sites (Miller 2011, pers. comm.) at
varying densities and was found to be
most prevalent at SH 94 and
compartment 16, Davy Crockett NF,
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respectively (Walker 2012, p. 2).
Without active or effective management,
Chinese tallow can reproduce quickly,
out-shading Neches River rose-mallow
and other native woody vegetation and
limiting its water and nutrient
absorption. Only select sites are being
actively managed for Chinese tallow,
but the species has not been
successfully eradicated at any of the
sites. This threat has led to declines at
all Neches River rose-mallow sites.
Therefore, based on the best scientific
and commercial data available on this
invasive, we conclude that invasion
from Chinese tallow is a threat across
the species’ range.
Coastal bermudagrass is not typically
found within the wetland habitats that
the Neches River rose-mallow prefers,
but three sites have persisting stands of
coastal bermudagrass: The Texas Land
Conservancy site, SH 204 ROW (Walker
2012, pers. comm.), and SH 94 or Boggy
Slough (Allen 2011a, pers. comm.). Site
visits to east Texas that included these
three sites in August 2012, did not
exhibit reduced numbers of Neches
River rose-mallow due to coastal
bermudagrass. Bahiagrass has not been
found at any Neches River rose-mallow
sites.
Coastal bermudagrass is an
introduced bermudagrass cultivar that
has been widely planted in the southern
United States for livestock forage. It is
adapted to a wide range of soil types
and climates and tolerates both drought
and periodic inundation (Burton and
Hanna 1985, p. 247), much like the
conditions of Neches River rose-mallow
habitat. In drier climates, this cultivar
will thrive along irrigation ditches and
streambeds, agricultural fields, and
roadside areas (Burton and Hanna 1985,
p. 247).
Due to its hybrid origin, coastal
bermudagrass produces very few viable
seeds and is established by planting
sprigs (rhizomes and stolons) (Stichler
and Bade 2012, p. 1); however once
established, coastal bermudagrass tends
to produce dense monocultures where
native species cannot persist. A lack of
management, including mowing, could
allow coastal bermudagrass to
monopolize Neches River rose-mallow
habitats such that the bermudagrass
would out-compete the rose-mallow for
water and nutrients and could out-shade
the Neches River rose-mallow. Along
ROWs, coastal bermudagrass and
bahiagrass are often included in
mixtures to re-seed ROWs in east Texas
(Adams 2013c, pers. comm.). The
wetter, low-lying areas of the ROW
where Neches River rose-mallow exists
are not generally planted with coastal
bermudagrass. TXDOT also mows along
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ROWs, potentially diminishing any
possible encroachment as coastal
bermudagrass and bahiagrass have not
been observed to cause declines in any
Neches River rose-mallow population.
The threat from coastal bermudagrass
and bahiagrass can have potential
impacts to native plants. However, only
three sites have coastal bermudagrass,
and bahiagrass is not present at any of
the sites. It does not appear that Neches
River rose-mallow has been negatively
impacted by either species as of yet or
will likely be impacted in the near
future. Therefore, based on the best
scientific and commercial data available
on coastal bermudagrass and bahiagrass,
and the lack of any observed impacts to
the Neches River rose-mallow, we
conclude that they are not threats to the
Neches River rose-mallow across its
range.
limit the abundance of these native tree
species. Two of the four sites were on
ROWs, and prescribed burning is not a
widely accepted method of ROW
maintenance. On the other two sites,
prescribed burning had not been
implemented. The TXDOT mows these
ROW sites, but mowing does not appear
to be an effective management tool
because these sites have both historic
and current observations of native
species encroachment.
Four of the 11 sites are impacted by
native species, the current management
techniques are not adequate for control
of native species, and effective
techniques need to be investigated.
Therefore, based on the best scientific
and commercial data available, the
effects of native encroachment by these
species pose an ongoing threat to the
Neches River rose-mallow.
Native Species
Historical and current encroachment
from native species has been observed
in Neches River rose-mallow habitat.
Two species, sweetgum and green ash
(Fraxinus pennsylvanica), are native,
deciduous trees of east Texas that have
been found at all Neches River rosemallow sites (Miller 2011, pers. comm.).
Four Neches River rose-mallow
populations monitored in 2011 were
overgrown with sweetgum and green
ash (Miller 2011, pers. comm.; TXNDD
2012a, pp. 1–11, 20–28). About 36
percent (4 of the 11) of the Neches River
rose-mallow’s populations are impacted
by competition and shading from native
sweetgum and green ash trees.
Sweetgum is found on a variety of
soils but grows best on moist, alluvial
clay and sandy loams of river bottoms
(Kormanik 2004, p. 790, in Burns and
Honkala 1990). Green ash also tolerates
a range of soils and in Texas is abundant
in clay or silty loams of floodplains
(Johnson 1980, in Gucker 2005, p. 15).
Both species also grow in full sun to
partially shaded habitats. Therefore,
both the sweetgum and green ash are
well adapted to the hydric alluvial soils
and partial to open canopies that the
Neches River rose-mallow needs. In the
absence of other competing species,
sweetgum and green ash can attain large
sizes (50–100 feet (15–30 m)) (Dickerson
2002, p. 1) and can reduce the open
canopy (Kirkman 1995, pp. 12, 15),
thereby shading out Neches River rosemallow.
Historically, natural fires generally
occurred every 1 to 3 years in east Texas
(Landers et al. 1990, p. 136; Landers
1991, p. 73) and controlled both native
and nonnative species. Naturally
occurring wildfires or prescribed fires
can be used as management tools to
Hydrological Changes
Habitat where Neches River rosemallow is found includes both
intermittent and perennial wetlands
along oxbows, sloughs, terraces, sand
bars, and other low-lying areas in
habitats with minimal standing water.
Wetlands are ecological communities
with hydric (flooded or saturated) soils.
Many wetland species, including the
Neches River rose-mallow, are adapted
to highly variable rates of water flow,
including seasonal high and low flows,
and occasional floods and droughts. For
example, the Neches River rose-mallow
likely requires high precipitation and
flowing water or flood events to
disperse seed (Warnock 1995, p. 20;
Scott 1997, p. 8; Reeves 2008, p. 3), and
although the Neches River rose-mallow
is adapted to persisting in dry
conditions during portions of the year,
a complete lack of water can diminish
seed production, range expansion, and
genetic exchange. As Neches River rosemallow habitat is so water-dependent,
hydrological changes can have huge
impacts. Some degree of hydrological
change has been seen at most of the
Neches River rose-mallow sites;
however, information on some of the
private land sites is lacking.
At the Boggy Slough site, which is
connected to the SH 94 site, natural
shifts of river and creek beds have left
meandering scars and remnant oxbows.
However, several levees upstream and
the creation of a duck hunting pond on
this site have changed the natural
landscape and flow patterns, thereby
converting seasonally inundated
wetlands to permanently flooded
wetlands (Miller 2011, pers. comm.).
Beaver activity, such as selective cutting
and damage to certain tree species, was
evident at the Boggy Slough site, but the
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56059
Neches River rose-mallow did not show
impacts.
On another private land site, The
Texas Land Conservancy site (referred
to as the Lovelady site in Table 4,
above), Neches River rose-mallow plants
were once observed lining the perimeter
of a flatwoods pond. However, after
2003, when a stock pond was
constructed (TXNDD 2012a, p. 18) in
what was likely part of an overflow
channel from Tantabogue Creek, the
natural surface hydrology was altered by
retaining overflow, preventing it from
draining south to the site containing
Neches River rose-mallow plants. The
Texas Land Conservancy was
considered a robust population;
however, in 2011, the Service and
TPWD botanists only observed 539
Neches River rose-mallow stems, most
of which were in relatively poor
condition (Miller 2011, pers. comm.).
All four Davy Crockett NF sites
(compartments 55, 16, 11, and 20)
censused in 2011 were completely dry
except for compartment 20, where a
small pond to the south drains into the
compartment (Miller 2011, pers.
comm.). Compartment 16 had altered
hydrological changes. In 2000, when the
Neches River rose-mallow was
introduced into a wetland on this
compartment, a beaver dam was
present. When the dam broke in 2002,
water infiltrated the site, and the
original hydrology was altered (TXNDD
2012a, p. 44). Plant numbers decreased
from 450 to 43 plants. It is unclear if
this decrease in plants was due directly
to the loss of the beaver dam; this needs
further research. The pine-oak forest on
adjacent private land west of
compartment 55 helps regulate the
amount, timing, and possibly the rate of
water flow into the compartment.
Therefore, any alteration of the pine
forest, through tree removal projects or
other habitat-altering activities, could
alter key hydrological characteristics of
this compartment. However, the
likelihood of tree removal projects or
habitat alteration activities on adjacent
lands is unknown but likely minimal.
Water development and construction
projects could also result in the
complete loss or inundation of water at
sites, threatening the Neches River rosemallow. In 1978, the Angelina and
Neches River Authority (ANRA)
proposed the construction of a reservoir
known as Lake Columbia (previously
known as Eastex), in Cherokee and
Smith Counties, Texas (ANRA 2012), to
supply water for five surrounding
counties (U.S. Army Corps of Engineers
(USACE), 2010, pp. 2–4, 3–43). The dam
for this reservoir would be constructed
on Mud Creek and would impound
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approximately 195,500 acre-feet (ac-ft)
(241 million cubic meters (mcm)) of
water in a reservoir reaching 14 mi (22.5
km) upstream (USACE 2010, p. 1–1). Up
to 85,507 ac-ft (1,105 mcm) of water
would be diverted from the downstream
flow of Mud Creek (USACE 2010, p. 1–
1).
According to the most current project
plans available in the draft
environmental impact statement (EIS), a
habitat evaluation procedures analysis
(a broad habitat-based approach to
assess environmental impacts of
proposed water and land resource
development projects) stated that it was
possible for the Neches River rosemallow to be in the permit area, if
habitat exists; however, the analysis did
not document any Neches River rosemallow in the permitted project area
(Walker 2011, pers. comm.; USACE
2010, p. 4–154). The ‘‘Permitted Project
Area’’ includes the footprint of the
normal conservation pool of the
reservoir below a certain elevation and
the limits of construction in the vicinity
of the dam, or a total of approximately
10,655 acres. The ‘‘Downstream Impacts
Area’’ was also analyzed in the EIS. This
area included the existing Mud Creek
100-year floodplain for a distance of
approximately 16 miles from below the
dam site to the confluence with the
Angelina River (USACE 2010, p. 1–4).
The extant Neches River rose-mallow
population found at the intersection of
SH 204 ROW and Mud Creek is within
the downstream portion of the project
that was analyzed. The SH 204 ROW
site is a perennial wetland where plants
generally remain inundated year round;
therefore, a change in the water level at
this site could make it unsuitable for
Neches River rose-mallow or could
restrict potential seed dispersal
mechanisms. Drought conditions could
also exacerbate the potential threats
from this project, and the reduced
downstream water flows could
completely extirpate the SH 204 ROW
site (USACE 2010, p. 4–154; Heger 2012,
pers. comm.).
Using the best scientific and
commercial data available, we
anticipate that the construction of the
Lake Columbia reservoir project will
divert water downstream, thereby likely
dewatering the SH 204 ROW site. The
agencies involved with the project are
still working on solidifying the project
details, and, therefore, we do not know
how much water will remain at this site
or if future water management practices
or decisions will allow for seasonal
flooding of water to this site.
Optimal habitat conditions for Neches
River rose-mallow include intermittent
or perennial wetlands that can be
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variable throughout the year, often
becoming surficially dry during the
summer and wet during the winter,
perhaps being exposed to water yearround. However, hydrological changes
that result in the complete loss or
inundation of water at the site threaten
the Neches River rose-mallow. Neches
River rose-mallow, despite its name, is
not found in deeper waters, unlike other
Hibiscus species, and the Neches River
rose-mallow is thought to need water at
some point of its life cycle for seed
dispersal. A complete loss of water at
any or all of the sites could restrict the
exchange of genetic material between
and among sites, thereby compromising
the species’ genetic integrity.
Although the severity of impacts from
beaver dams to the Neches River rosemallow could be high, the level of
exposure to this stressor is low.
Consequently, we do not consider
beaver dams a threat at this time.
However, the severity of altered
hydrology as a whole is high and the
exposure of this threat is present
throughout the species’ range.
Consequently, we have determined that
altered hydrology is a threat now and
will continue to be a threat in the nearfuture.
Upgrades and Construction for ROWs,
Roads, Bridges, and Other Structures
Right-of-way populations are
vulnerable to bridge and road
expansion, new road construction, and
upgrade projects. These activities could
impact the sites’ hydrology, soil
stability, wetland and riparian
vegetation, and water quality.
Hydrological changes, erosion, and
changes in the associated native
vegetation due to ROW and road
upgrades and construction projects are
threats to the species (as described in
detail in the ‘‘Nonnative Species,’’
‘‘Native Species,’’ and ‘‘Hydrological
Changes’’ sections, above). We do not
have information on how sedimentation
and changes in water quality could
impact Neches River rose-mallow;
however, increased siltation within the
water column is the major pollutant of
wetlands in the United States (Baker
1992; USEPA 1995).
In 2005, a proposed bridge
replacement on SH 230 ROW would
have altered approximately 4.91 ac (2
ha) of Neches River rose-mallow habitat
south of the ROW and 0.07 ac (0.03 ha)
north of the ROW (Adams 2005, p. 1),
but the TXDOT implemented avoidance
measures. Bridge replacement and road
expansion projects are continuing along
SH 94 ROW, but as of 2011, had not
progressed into Neches River rosemallow habitats (Adams 2011c, pers.
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comm.). For this project, TXDOT is
using temporary culverts and silt
fencing to reduce sedimentation, and
the Neches River rose-mallow site has
been fenced off to prevent access.
Regardless of these minimization
techniques, sedimentation was evident
along SH 94 ROW (Walker 2012, p. 2).
Potential road projects are mainly
restricted to ROW easements and may
potentially impact three of the 11 extant
populations. Roadwork along SH 230 is
occurring, and based on communication
with the TXDOT, there will likely be
only one project in road ROWs within
the Neches River rose-mallow sites.
These activities are currently being
implemented or will be in the near
future. As a result, the impacts to
Neches River rose-mallow could be
high, as an entire population could be
removed as a result of these activities.
Consequently, we conclude that SH
ROW maintenance, bridge maintenance,
and other structural projects are a threat
to Neches River rose-mallow
populations now and will continue to
be a threat into the future.
Silviculture
Pine plantations in east Texas are
established mainly on uplands that are
managed to mimic old fields or grassy
savannas (Fox et al. 2007, p. 340). Site
preparation may include anchor
chaining, chopping, burning, root
raking, shearing, and disking (Balmer
and Little 1978, p. 60). One Neches
River rose-mallow population on private
property south of SH 230 was extirpated
when the site was converted to a pine
plantation sometime after 2003 (Poole
2011b, pers. comm.; TXNDD 2012a, pp.
61–67). Three additional sites in or near
Neches River rose-mallow populations
have shown evidence of habitat-clearing
activities to prepare land for harvesting
trees, including: Adjacent land south of
the Davy Crockett NF compartment 55,
Houston County; an extirpated site
located south of the extant Lovelady
site, Houston County; and the privately
owned site at Champion, Trinity
County.
Although silviculture impacts have
occurred in the past, the likelihood that
silviculture activities (including landclearing activities and actual planting of
trees) will occur in the near future is
very low on the occupied units,
including the three ROW sites and on
the four USFS sites. In addition, the
wetland habitat does not necessarily
exclude silviculture from occurring on
sites, but wetlands are not usually
considered the best sites for pine
planting. Therefore, we conclude that
silviculture activities are currently not a
threat to the Neches River rose-mallow.
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Herbicide Use
Herbicide treatments are increasingly
popular because they remove unwanted
plant growth without causing soil
erosion from the site; however,
herbicide use increases incidents of
water pollution and aerial drift to
nontarget sites (Balmer and Little 1978,
p. 63). There have been several
instances where herbicide impacts to
Neches River rose-mallow plants on
ROWs and on privately owned lands
have been documented. Neches River
rose-mallow populations may also be
potentially impacted by herbicides
applied to pine plantations that drift
into the Neches River rose-mallow
habitat. Normal rainfall and flood events
can unintentionally disperse herbicides
downstream, impacting individual
plants or whole populations, depending
on the nature of the herbicide.
Three subpopulations in Trinity
County along SH 230 experienced
impacts from herbicide spraying. One
subpopulation with approximately 50
plants, on private property south of SH
230, was extirpated by herbicide use
(Service 2010b, p. 7). Herbicide drift at
a second subpopulation along SH 230
(Gordon 2009, pp. 3–4) caused the ROW
population to decline from 14 plants in
1999 (Poole 2001, p. 2) to zero plants in
2002 (Miller 2011, pers. comm.).
Herbicide damage was evident at a third
subpopulation along SH 230 ROW, and
could have been the result of herbicide
use by the private landowner south of
SH 230 (what is now planted in pine),
but this has not been confirmed. In
2012, a graduate student from Stephen
F. Austin State University noted Neches
River rose-mallow at this site, but this
needs to be confirmed.
The TXDOT used herbicides to
remove woody vegetation from ROWs in
the past (Miller 2005, pers. comm., in
Service 2006, p. 7; Adams 2011c, pers.
comm.), but mechanical clearing
methods have largely replaced the use
of herbicides in these ROW areas.
Impacts from herbicide applications to
Neches River rose-mallow have not been
documented at any of the four USFS
compartments. The USFS Revised Land
and Resource Management Plan for
National Forests and Grasslands in
Texas restricts the use of nonaquatic
herbicides unless hand-applied (United
States Department of Agriculture 1996,
p. 153).
Exposure to herbicides, in
conjunction with silviculture activities,
is a threat to the Neches River rosemallow, as it has impacted seven of the
11 populations (64 percent). While the
majority of Neches River rose-mallow
populations are on State or Federal
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land, all are adjacent to private lands.
Even though the State and the USFS do
not actively use herbicides, private
landowners do. Consequently, herbicide
overspray from private land could
impact all existing Neches River rosemallow populations. The severity of
herbicide use effects to the Neches River
rose-mallow, in combination with
silviculture practices, is high, as seven
of the 11 populations have been
impacted by these activities. These
activities are current and ongoing
threats. Consequently, exposure to
herbicides is a current and near future
threat to the Neches River rose-mallow.
Trampling and Herbivory by Feral Hogs
and Cattle
Feral hogs (Sus scrofa) were first
introduced to the mainland of North
America (Wood and Barrett 1979, pp.
237, 238) in Texas in 1542, although
large-scale introductions did not occur
until the 1930s (Isle and Hellgren 1995,
p. 793). While these omnivores dig in
the soil in search of roots, tubers, and
invertebrates, they can inadvertently
cause damage to other food resources
and habitat. Feral hogs forage by turning
over soil with their snouts, creating
mounds and depressions (Arrington et
al. 1999, p. 535). Hogs transition from
foraging in oak stands during winter
months, to foraging in swamp and
marsh edges during the summer months
to feed on grasses, sedges, tubers, and
roots (Wood and Roark 1980, pp. 507–
509). Feral hogs are able to travel long
distances to feed, and often uproot vast
areas of habitat. Feral hogs reach sexual
maturity at 6 to 8 months (Wood and
Barrett 1979, p. 242), and have large
litter sizes. However, uprooting of
Neches River rose-mallow has not been
observed (Creech 2011a, pers. comm.;
Miller 2011, pers. comm.).
There are both historic and current
records of damage to Neches River rosemallow habitat from feral hogs. Damage
of habitat by feral hogs has historically
been recorded at Mill Creek Gardens
(Creech 2011a, pers. comm.; Miller
2011, pers. comm.) and on all four Davy
Crockett NF sites. Until 2012, only
tracks and damage to habitat have been
the most noted type of destruction;
however, current damage to Neches
River rose-mallow plants was observed
in compartments 16 and 20 of the Davy
Crockett NF, where feral hogs had
broken and flattened plants (Walker
2012, pers. comm.). Large groups of feral
hogs were observed in Neches River
rose-mallow sites within compartments
55 and 16 of the Davy Crockett NF
(Walker 2012, pers. comm.). Habitat
damage is rangewide, and although
Neches River rose-mallow may not the
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primary target during foraging activity,
plants have been damaged.
Although the Neches River rosemallow grows adjacent to permanent
standing water or may occur within
infrequently flooded areas, this does not
limit the access of feral hogs. Further,
drought may enhance accessibility to
Neches River rose-mallow sites, thus
increasing their susceptibility to
trampling by feral hogs. Unmanaged
feral hog populations can lead to
increased soil disturbance and impacts
to the native vegetative community,
which could create prime conditions for
nonnative species to invade. Current
feral hog damage has been documented
at four of the 11 Neches River rosemallow sites. Feral hogs are a present
threat and will likely continue to be a
threat in the near future. However, at
this time the severity of impacts to the
Neches River rose-mallow is low.
It is estimated that livestock grazing
has damaged 80 percent of stream and
riparian ecosystems in the southern
United States (Belsky et al. 1999, p.
419). The damage includes increased
sedimentation, decreased water quality,
and trampling and overgrazed stream
banks where succulent (high water
content) forage exists (Armour et al.
1994, p. 10; Fleischner 1994, p. 631;
Belsky et al. 1999, p. 419). Trampling
causes soil compaction and damage to
both above- and below-ground
vegetative plant structures and increases
soil erosion (Warren et al. 1986, p. 491).
Livestock owned by a neighboring
landowner were observed on The Texas
Land Conservancy’s Lovelady site in
2011. The Neches River rose-mallow at
the Lovelady site suffered severe
documented herbivory where stems had
been eaten almost to the ground
(TXNDD 2012a). The Texas Land
Conservancy has attempted to exclude
these livestock, and has proposed
constructing an exclusion fence around
the current location of the Neches River
rose-mallow population; however,
funding has not been secured (Dietz
2011, pers. comm.). The Neches River
rose-mallow at Lovelady is concentrated
along a low area leading into a stock
pond (Miller 2011, pers. comm.). Only
one of 11 sites (9 percent of the total
known population) has shown damage
from cattle herbivory. Trampling has not
been observed at the Lovelady site or
any other. Drought could exacerbate
herbivory, as was seen in the severe
drought of 2011, which could lead to an
increase in trampling. The immediacy
and severity of herbivory to the Neches
River rose-mallow is high, but the
exposure to herbivory is low. Therefore,
we conclude that herbivory is not a
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Natural Gas Pipelines and Well Activity
The Haynesville or Bossier and Eagle
Ford Shale formations in east Texas are
currently being developed for oil and
natural gas production. The Texas
Railroad Commission regulates the oil
and natural gas industry in the State of
Texas and maintains a database with
proposed activities. Several of the
counties with known populations of
Neches River rose-mallow, including
Houston, Trinity, Nacogdoches, and
Cherokee Counties, may be subject to
increased oil and natural gas
exploration in the future (Texas
Railroad Commission 2012). However,
oil and gas exploration was not
observed on or directly adjacent to any
of the Neches River rose-mallow
populations that the Service observed in
2011, and currently there are no
proposals near extant Neches River rosemallow populations. Therefore, we
determine that oil and natural gas
exploration activities are not currently a
threat to the Neches River rose-mallow.
from the previous 3 years of drought,
including changes in leaf morphology,
dead plants at specific sites, reduced
seed production, and lower water levels
in perennial wetlands. In addition, one
site (The Texas Land Conservancy site)
showed evidence of herbivory by
livestock. The survival of Neches River
rose-mallow populations during
previous drought cycles may have been
aided by its greater abundance and by
greater habitat contiguity. Loss of
habitat contiguity impedes the
recolonization of sites from neighboring
seed sources following a catastrophic
loss, such as from drought. More
frequent droughts will further
exasperate these impacts to the Neches
River rose-mallow.
With climate change projections of
warmer and more frequent droughts,
and more extreme precipitation events,
impacts to the Neches River rosemallow will continue. The severity of
impacts to the Neches River rosemallow is high, as all populations will
be impacted. Further, this threat is
current and will continue into the near
future.
Climate Change
We discuss the topic of climate
change in greater detail under ‘‘A. The
Present or Threatened Destruction,
Modification, or Curtailment of Its
Habitat or Range’’ for the Texas golden
gladecress (which, like the Neches River
rose-mallow, is also found in east
Texas). In summary, the consensus of
climate models predicts that the climate
in east Texas will become warmer and
will experience both more frequent
droughts and more extreme
precipitation events. Diggs et al. (2006,
p. 80) states that climate extremes,
particularly drought and low
temperatures, have greater influence
than average conditions do on excluding
nonadapted species. Extreme
precipitation events (such as tropical
storms) may adversely affect the Neches
River rose-mallow by altering flow
regimes and by temporarily increasing
the depth of its wetland habitat to a
level at which the species cannot
survive. A warmer climate with more
precipitation extremes may also
increase competition from native and
nonnative invasive plant species
(Service 2010b, p. 8). The timing of
precipitation is also crucial for the
Neches River rose-mallow, as seed
dispersal is likely dependent on flowing
water.
Neches River rose-mallow has shown
evidence of damage from drought
conditions. In October 2011, all Neches
River rose-mallow populations and
habitats showed evidence of damage
Other Conservation Efforts
Three populations of the Neches River
rose-mallow exist along SH ROWs in
Houston, Trinity, and Cherokee
Counties. The TXDOT and TPWD
currently operate under a revised 1988
memorandum of understanding (MOU)
that governs management actions
targeting conservation of listed species
and key habitats on SH ROWs that may
potentially affect natural resources
within facilities owned or managed by
TPWD. Because the Neches River rosemallow was not a listed species, the
MOU relates to protection of Neches
River rose-mallow habitat if the
proposed projects include the following:
Contains 1.0 ac (0.54 ha) of new ROW
within floodplains or creek drainages;
requires channel modifications to
streams, rivers, or water bodies; and
requires realignment of channels with
mature woody vegetation; or projects
that may impact mature woody or native
vegetation (Texas Administrative Code
1999, p. 4). Although a formal
mechanism via the MOU has been
established to review projects and
alleviate or eliminate threats to Federal
and State-listed species and key
resources, there have not been any
projects that fit these standards that
have been recently reviewed under the
MOU.
Five populations, including a portion
of the SH 94 site, are located on private
lands. Historically, two candidate
conservation agreements were formed
between the Service and Champion
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International (Champion) in 1998, and
with Temple-Inland Forest Products
(Temple-Inland) in 2002, to conserve
the Neches River rose-mallow on both
sites. The candidate conservation
agreements have expired, and private
landowners are not restricted by
guidelines outlined those agreements.
Champion’s 5-year candidate
conservation agreement included 40 ac
(16.2 ha) of wetland and was located
east of White Rock Creek in Trinity
County (Champion site in Table 4).
Management guidelines included:
Maintain 100-ft (30-m) buffer around
occupied and dispersal habitat, free
from timber harvesting, site preparation,
and reforestation activities; minimize
hydrological alterations; inhibit filling
or pilling debris or material on
populations; and apply herbicides only
by hand and at times of little or no wind
(Service 1998, p. 4). The Champion
property was sold to Temple-Inland in
2001, and in 2004, the candidate
conservation agreement expired (Service
2010b, p. 9). The Temple-Inland
candidate conservation agreement
covered an area that has a 20-ac (8.1-ha)
wetland with Neches River rose-mallow
(Boggy Slough site in Table 4); the
plants declined due to drought and
alteration of an onsite wetland. A
smaller wetland with Neches River rosemallow plants was drained in order to
regulate water levels of the larger
wetland, which was to be used by
Temple-Inland for recreational hunting
(Service 2002, p. 3; Service 2010b, p. 9).
The Temple-Inland candidate
conservation agreement was valid from
2002–2004. Contact was made with the
owners, and the Service and TPWD
visited the site in October 2011. Plants
appeared healthy, but nonnative and
native species encroachment into
Neches River rose-mallow habitat was
observed (Miller 2011, pers. comm.).
Four known sites lie within the Davy
Crockett NF, which is managed under
the Revised Land and Resource
Management Plan. The USFS considers
the Neches River rose-mallow a
sensitive species. Actions occurring on
USFS property must not result in a net
loss of species viability or create
significant trends toward the need for
Federal listing. However, USFS
standards and guidelines in the plan are
not mandatory and do not address all
threats pertaining to the Neches River
rose-mallow.
The Lovelady site is owned by The
Texas Land Conservancy, once known
as the Natural Area Preservation
Association. Thirty acres (12 ha) of land
were purchased in 2004, located north
of SH 230 (The Texas Land Conservancy
2011). Purchase of this easement on
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private land was specifically for the
conservation of the Neches River rosemallow; however, plants occur on
private land, and they are not offered
protection under the Act unless there is
a Federal nexus. However, The Texas
Land Conservancy had initiated a
voluntary effort to construct a cattleexclusion fence, but funds were lacking
and the project was not completed
(Dietz 2011, pers. comm.). The
introduced site at Mill Creek Gardens
was created in 1995, as a conservation
easement by a private donor (Stephen F.
Austin State University 1999, p. 1), and
was used as an experimental plot to test
fertilizer and mulching effects on the
Neches River rose-mallow (Scott 1997,
pp. 6–7). This site is informally
managed through mowing and burning
regimes prescribed by Stephen F. Austin
State University staff, but encroachment
from native woody species has been
observed in the past (Creech 2011c,
pers. comm.). The Neches River rosemallow was last observed in 1980 at the
Harrison County site and the site has
not been revisted since then due to a
lack of accessibility. The Neches River
rose-mallow was last observed at the
Camp Olympia site in 1978. The site has
been revisited in 1992 and 1993, but has
not been observed (Warnock 1995, pp.
6, 8; TXNDD 2012a, pp. 58–60).
Introductions onto Mill Creek Gardens
and the Pineywoods Native Plant Center
on the Stephen F. Austin State
University campus have provided
researchers the opportunities to study
the species, including its affinity for
hybridization. Seed has also been
collected by the Mercer Arboretum in
Ft. Collins, Colorado.
Summary of Factor A
Based on our evaluation of the best
available scientific and commercial
data, we conclude that the present loss
and modification of the Neches River
rose-mallow’s habitat is a threat that has
significant impacts to the species’
continued survival. Threats include
competition for light and nutrients by
native and nonnative invasive plant
species, altered hydrology, herbicide
drift, and trampling by feral hogs. These
threats may be exacerbated by future
road and bridge construction and
maintenance projects. We determine
that livestock grazing is not a threat to
the species. Although silvicultural
practices have caused some prior
impacts to the species, we do not
anticipate that silviculture activities
will continue to be a threat. The
activities related to exploration and
development of oil and natural gas wells
are not currently a threat to the species.
Effects of climate change may be
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exacerbated by effects from other
threats. Additional conservation
measures that had protected habitat and
certain actions on privately owned land
have expired and no longer provide
protection to habitat of the Neches River
rose-mallow. Therefore, we conclude
that habitat loss, destruction, and
modification is a threat to the Neches
River rose-mallow rangewide both now
and in the future.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
The showy flowers produced by the
genus Hibiscus make it of high
horticultural interest (Service 2010b, p.
8) to Hibiscus enthusiasts (Warnock
1995, p. 25; Poole et al. 2007, p. 265).
Hybridization within genus Hibiscus is
repeatedly done in the nursery trade
(Creech 2011a, pers. comm.) to produce
different colored flowers and modify
other traits that may be of commercial
interest. Ornamental landscaping
companies sell Neches River rosemallow plants online (Creech 2011a,
pers. comm.). Neches River rose-mallow
plants are easy to cultivate from
cuttings, and having plants available for
sale in the nursery trade reduces
collecting pressures of the species from
the wild (Creech 2011a, pers. comm.).
Plantings of Neches River rose-mallow
into garden settings are standard, and
placement within close proximity to
wild populations has not been recorded
or observed.
Mercer Arboretum collected seed in
1993, 1994, 1996, 1997, and 2003; these
seeds, as well as living plants, are being
maintained at the Mercer Arboretum
(Tiller 2011, pers. comm.). A portion of
the seeds collected were grown out in
the Mercer Arboretum Rare and
Endangered Gardens, where they have
remained; seeds and plants have not
been transplanted back into the wild
populations (Tiller 2011, pers. comm.).
Neches River rose-mallow seed was also
sent to the National Seed Storage
Laboratory in Fort Collins, Colorado, for
long-term storage for conservation
purposes (Ellis 2011, pers. comm.).
The scientific and horticultural
communities have collected Neches
River rose-mallow seeds and plants
from wild populations; however, we
have no evidence that suggests that
collection has depleted the seed bank or
has adversely affected populations.
Plants are easily cultivated, and the
species is well established as a nursery
trade plant, thereby reducing potential
collection pressure. Based on the best
scientific and commercial data
available, we conclude that collection
for recreational, scientific, or
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educational purposes is not a threat to
the Neches River rose-mallow and is not
likely to become one in the future.
C. Disease or Predation
Leaves and stems of plants in the
Hibiscus family (Kroll 1991, p. 392;
Everitt et al. 1999, pp. 177–193) are
often consumed by white-tailed deer
(Odocoileus virginianus) (Moreland
2005, p. 48). Cattle also consume the
stems but typically to a lesser degree
than white-tailed deer (Everitt et al.
1999, pp. 187–193). In 1993, evidence of
herbivory was present at four of the 11
Neches River rose-mallow
subpopulations at Lovelady (Warnock
1995, p. 18) and in 2010, at
compartment 20 (Allen and Duty 2010,
p. 3). In 2011, at five of the 11
populations, aboveground portions of
the Neches River rose-mallow, mainly
the tips, were grazed by cattle, with the
most intense herbivory occurring at the
Lovelady site; cattle on adjacent land
were the likely culprit. Herbivore
consumption of plants could decrease
the reproductive success of the Neches
River rose-mallow (Adler et al. 2001, p.
1). Only at compartment 20 on the Davy
Crockett NF was the evidence of
browsing on the flowers observed (Allen
and Duty 2010, p. 3); however, the
species is able to produce secondary
growth, which increases and
strengthens the girth rather than the
height of the plant (Strauss and Agrawal
1999, p. 179; Bailey 2006, p. 415).
Insect damage and predation has been
observed on Neches River rose-mallow
plants in several populations; however,
regrowth of foliage after herbivory
incidents may indicate that the Neches
River rose-mallow is adapted to
herbivory (Strauss and Agrawal 1999, p.
179). Ninety percent of the first foliage
of Neches River rose-mallow leaves at
Lovelady had been consumed by insects
(Service 2010b, p. 8) with insect
predation also seen on compartment 11
plants in 2006 (Philipps 2009, p. 1). The
scentless plant bug (Niesthrea
louisianica) was observed on plants in
compartment 55 (Miller 2011, pers.
comm.). This bug is known to deposit
egg masses on stems, leaves, flower
parts, buds, and seed pods of Hibiscus
species (Wheeler 1977, p. 632), but to
also consume Hibiscus seeds (Toth
2007, p. 6). Holes were observed on
several Neches River rose-mallow plants
on all Davy Crockett NF sites (Miller
2011, pers. comm.) and were likely
caused by this plant bug. Larval forms
of the Hibiscus sawfly (Atomacera
decepta) can consume Neches River
rose-mallow seed pods in herbaria, but
have not been noted to affect wild
populations (Wieland 1995, p. 1; Creech
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2011a, pers. comm.). However, these
bugs are not considered a significant
pest because the damage to the plants is
minor (Toth 2007, p. 6).
Changes in precipitation are not well
understood in relationship to insect
herbivory (Bale et al. 2002, p. 2).
Drought conditions may exacerbate
consumption of the vegetative and floral
parts if other food resources within the
plant community become scarce.
Temperature shifts related to climate
change may trigger corresponding insect
population shifts. Impacts from insect
population shifts cannot be predicted;
however, if conditions favor the growth
of insect populations, the effects of
insect herbivory on the Neches River
rose-mallow could increase. Drought
could exacerbate the consumption of
leaves and stems if preferred plants
were not available, but we conclude that
ungulate (hoofed animal) herbivory is
an insignificant stressor to the Neches
River rose-mallow.
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Summary of Factor C
Mammalian herbivory has affected the
majority of sites; however, grazing
pressures are largely attributed to the
lack of other available food resources
during periods of drought. Neches River
rose-mallow recovers quickly from
herbivory incidents and can produce
secondary growth, minimizing the
overall negative effects of mammalian
herbivory. This type of herbivory is not
considered to be a threat to the species.
Insect herbivory was also observed on
several of the sites and was not
rangewide, but, with anticipated climate
change shifts in temperature and the
likelihood that insect populations will
increase, we conclude that insect
predation is a minor stressor that will
likely continue into the future, but it is
not a threat to the species.
D. The Inadequacy of Existing
Regulatory Mechanisms
Under this factor, we examine
whether existing regulatory mechanisms
are inadequate to address the threats to
the species discussed under the other
factors. Section 4(b)(1)(A) of the Act
requires the Service to take into account
‘‘those efforts, if any, being made by any
State or foreign nation, or any political
subdivision of a State or foreign nation,
to protect such species . . . .’’ In
relation to Factor D under the Act, we
interpret this language to require the
Service to consider relevant Federal,
State, and tribal laws, regulations, and
other such mechanisms that may
minimize any of the threats we describe
in threat analyses under the other four
factors, or otherwise enhance
conservation of the species. We give
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strongest weight to statutes and their
implementing regulations and to
management direction that stems from
those laws and regulations. An example
would be State governmental actions
enforced under a State statute or
constitution, or Federal action under
statute.
Having evaluated the significance of
the threat as mitigated by any such
conservation efforts, we analyze under
Factor D the extent to which existing
regulatory mechanisms are inadequate
to address the specific threats to the
species. Regulatory mechanisms, if they
exist, may reduce or eliminate the
impacts from one or more identified
threats. In this section, we review
existing State and Federal regulatory
mechanisms to determine whether they
effectively reduce or remove threats to
the Neches River rose-mallow.
Davy Crockett NF lands are federally
owned and managed by the USFS for
the general public. Four populations of
the Neches River rose-mallow occur on
the Davy Crockett NF. The Davy
Crockett NF classifies the Neches River
rose-mallow as a Regional Forester’s
Sensitive Species (Philipps 2012, pers.
comm.), and habitat is within
Management Area Zone 4, according to
the Revised Land and Resource
Management Plan for National Forests
and Grasslands in Texas (USDA 1996,
entire). This management zone includes
the bed, bank, and water resources of
the rivers, perennial and intermittent
streams and wetlands, and their
adjacent areas (United States
Department of Agriculture 1996, p. 145).
This area is managed to maintain the
role and function of aquatic, riparian,
and wetland ecosystems while
providing opportunities for compatible
multiple uses and will be managed to
meet recommendations stated in the
Texas Wetland Plan (TPWD 1988) and
Best Management Practices established
by the State (United States Department
of Agriculture 1996, p. 151). Relative
Management Area Zone 4 standards and
guidelines include: Maintenance or
restoration of native plant communities;
prohibition of nonaquatic herbicide
uses, except hand applications or
noxious weed control following
restriction on the herbicide label; and
use of prescribed fire when necessary to
enhance riparian vegetation or wildlife
habitat (United States Department of
Agriculture 1996, pp. 153, 155).
Herbicides are not currently being used
on the Davy Crockett NF and have been
replaced by prescribed fire, with the
goal of routinely burning compartments
every 3 years (Stiles 2011, pers. comm.).
As discussed previously (see
‘‘Nonnative Species’’ under the Factor A
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discussion), routine fires may play a
role in reducing Chinese tallow. Actions
that may affect Neches River rosemallow habitat need to be assessed
using these standards and guidelines
because these are considered regulations
that need to be followed (Philipps 2012,
pers. comm.). The encroachment of
nonnative and native vegetation in
Neches River rose-mallow habitat is not
addressed in the Revised Land and
Resource Management Plan for National
Forests and Grasslands in Texas;
however, the application of prescribed
fire in some areas may benefit the
Neches River rose-mallow.
The Neches River rose-mallow is
considered by the USFS to be a sensitive
species on the Davy Crockett NF. A
sensitive species is defined as one not
yet warranting listing as an endangered
or threatened species, but which is
sufficiently rare that its future survival
is of concern (USFS Manual 2670,
2005). The management objectives
described in USFS Manual 2670 are to
develop and implement management
practices to ensure that species do not
become endangered or threatened
because of USFS actions, including:
Maintain viable populations of all
native and desired nonnative wildlife,
fish, and plant species in habitats
distributed throughout their geographic
range on NF System lands; and develop
and implement management objectives
for populations or habitat of sensitive
species or both. Application of USFS
Manual 2670 standards are only
guidelines, and are not mandatory.
However, the USFS must consider the
effects of their actions on the viability
of sensitive species through the National
Environmental Policy Act (NEPA; 42
U.S.C. 4321 et seq.) process. As defined
by USFS policy, actions must not result
in loss of species viability or create
significant trends toward the need for
Federal listing. This designation does
not provide specific habitat or species
protection, but does provide some
benefits to the species because of
increased awareness and evaluating
projects that may affect the species
through the NEPA process. Specific
threats to the Neches River rose-mallow
are not addressed with this designation.
Existing regulatory mechanisms do
not provide protection for plants on
private lands. Neches River rose-mallow
populations on Davy Crockett NF lands
only receive some protection from
habitat modification. In addition, not all
threats are addressed, such as
encroachment of nonnative and native
species into Neches River rose-mallow
habitat. The designation as a sensitive
species for the Neches River rosemallow does not address the threats
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specific to the species. Only when the
species is listed under the Act will the
USFS be required to consult on projects
that could impact the species or its
habitat. Therefore, based on our review
of the best scientific and commercial
data available, we conclude that existing
regulatory mechanisms provide some
protection against threats, but these
mechanisms do not address or
ameliorate all of the threats.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Small Population Size
Small population size can result in a
decrease in genetic diversity due to
genetic drift (the random change in
genetic variation each generation) and
inbreeding (mating of related
individuals) (Antonovics 1976, p. 238;
Ellstram and Elam 1993, pp. 218–219).
Genetic drift can decrease genetic
variation within a population by
favoring certain characteristics and,
thereby, increasing differences between
populations (Ellstram and Elam 1993,
pp. 218–219). Self-fertilization and low
dispersal rates can cause low genetic
diversity due to inbreeding (Antonovics
1976, p. 238; Barrett and Kohn 1991, p.
21). This decreased genetic diversity
diminishes a species’ ability to adapt to
the selective pressures of a changing
environment (Ellstrand 1992, p. 77;
Newman and Pilson 1997, p. 360).
Klips (1995) looked at the genetic
affinity of the Neches River rose-mallow
compared with the two other congeners
(similar) species, Hibiscus moscheutos
and H. laevis. In his study, Klips
concluded both H. dasycalyx and H.
laevis are genetically more similar than
H. moscheutos. Mendoza created the
genetic fingerprints for all three
congener species to help determine the
level of hybridization within and among
populations. Both studies observed wild
plants that appeared to be hybrids;
however, neither Klips nor Mendoza
studied the occurrence of hybridization
among the populations of the Neches
River rose-mallow. There is no evidence
that Neches River rose-mallow
populations are experiencing genetic
drift or inbreeding. We conclude that
small population size is not a threat to
the Neches River rose-mallow.
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Hybridization
The genus Hibiscus easily hybridizes
in the nursery trade (Creech 2011a, pers.
comm.). Hybridization under natural
conditions has not been verified, but
several Neches River rose-mallow sites
contain individuals that may be
products of crosses between the Neches
River rose-mallow with H. laevis or H.
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moscheutos. In some locations, H. laevis
or H. moscheutos, or both, grow in close
proximity to the Neches River rosemallow. These plants have leaves,
flowers, and floral parts resembling both
parent species (Service 2010b, p. 3;
TXNDD 2012a, entire). Other species
accounts, including our candidate
notices of review and anecdotal
accounts from USFS, TPWD, and other
botanists, conclude that there is the
potential that hybrids may exist at most,
if not all, of the sites; however, genetic
studies have not confirmed that this
phenomenon is occurring. So far, these
are only observations, and no genetic
studies have taken place to verify if
hybridization is occurring. The
University of Texas-Tyler is researching
the hybridization issue for Neches River
rose-mallow and its impacts on the
population; however, the project is only
in its infancy, and no results have been
determined. Therefore, we do not
consider hybridization to be a threat to
the Neches River rose-mallow.
Conservation Efforts To Reduce Other
Natural or Manmade Factors Affecting
Its Continued Existence
We have several examples of
voluntary conservation efforts that are
currently underway, or which took
place in the past, that directly, or
indirectly, assist the Neches River rosemallow by addressing the impacts of
habitat loss and degradation, or low
population and individual plant
numbers. See description under the
Factor A analysis above.
Cumulative Effects From Factors A
Through E
The threats that have the most severe
impacts to the Neches River rosemallow and its habitat involve the loss,
destruction, modification, and
curtailment of habitat. The rangewide
and imminent threat from nonnative
species encroachment (mainly Chinese
tallow) and native woody species
(sweetgum and green ash) will likely
continue if regulatory mechanisms are
not employed. Alteration of natural
hydrological features of Neches River
rose-mallow is an ongoing and potential
threat, having rangewide impacts.
Trampling and herbivory also impact
the Neches River rose-mallow.
Threats discussed in this finding
could work in concert with one another
to cumulatively create situations that
potentially impact Neches River rosemallow beyond the scope of the
combined threats that we have already
analyzed. Specifically, threats may be
exacerbated by the effects of ongoing
and future climate change, especially
the projected increases in temperature
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and decreases in precipitation that may
increase the frequency and severity of
droughts. Although the Neches River
rose-mallow is adapted to being dry
during portions of the year, a complete
lack of water can diminish its ability to
expand its known range and reduce its
genetic exchange. Further, climate
change could lead to an increase in
nonnative species, because nonnative
species can typically tolerate a wider
range of habitat conditions outside of
those that are suitable for the Neches
River rose-mallow. Drought conditions
can increase the susceptibility of sites to
be impacted from trampling from feral
hogs, such that observations of broken
and flattened plants would increase.
The reproductive capabilities of feral
hogs and their ubiquitous foraging
behavior allows them to adapt well to
drought conditions. Herbivory from
cattle, or white-tail deer, would also
increase in concert with future effects of
climate change. Hydrological alterations
combined with drought conditions
could cause or intensify herbivory. This
phenomenon was only observed at The
Texas Land Conservancy site in 2011 by
cattle, where drought likely increased
the grazing pressures not normally
experienced by the Neches River rosemallow within this site. A reduction in
the height of Neches River rose-mallow
stems could increase its vulnerability to
browsing by cattle. The drought
conditions of 2011 caused decreased
heights in Neches River rose-mallow
plants; this, combined with the lack of
a cattle exclusion fence on an adjacent
land to The Texas Land Conservancy,
likely increased the risk of herbivory.
When normal rainfall resumes and
preferred forage sources become
available, herbivory would likely
decrease.
Summary of Factors
The primary factors threats to Neches
River rose-mallow are nonnative species
encroachment at all sites; invasion of
sites by native woody species, causing
shading and increased competition for
resources; ongoing and potential
changes to key hydrological features of
the species’ habitat; future construction
and ROW projects; and aerial herbicide
drift incidents. These factors pose
imminent threats to the species because
they are ongoing or are likely to occur
in the near future. Since the Neches
River rose-mallow is endemic to
intermittent and perennial wetlands,
drought can exacerbate all of the
existing threats.
Determination
Based on our review of the best
scientific and commercial data
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available, we conclude that the Neches
River rose-mallow is likely to become an
endangered species within the
foreseeable future and, therefore, meets
the definition of a threatened species.
This finding, explained below, is based
on our conclusions that the Neches
River rose-mallow’s primary threats are
imminent, thus causing the species to
exhibit low viability as characterized as
having only one site close to meeting its
conservation goals. Significant factors
that support this determination include
the following:
• The significant and ongoing threat
from nonnative species at all sites
(Factor A);
• The encroachment of habitat from
woody natives (Factor A);
• The potential extirpation of an
occupied Neches River rose-mallow site
from a reservoir project (Factor A);
• Ongoing and potential changes to
key hydrological features of the species’
habitat (Factor A);
• The potential threat from future
construction and ROW projects (Factor
A);
• The trampling from feral hogs
(Factor A);
• Ongoing threats from aerial
herbicide drift incidents (Factor A); and
• Sustained drought that affects
habitat quality and reproductive output
of the species (Factor A).
We relied on Pavlik’s Minimum
Viable Population analysis tool (1996,
pp. 127–155) and species experts to
determine the conservation goals of the
species. Based on the best known and
available scientific information on the
species’ life-history and reproductive
characteristics, we concluded that the
conservation goals for the Neches River
rose-mallow included 10 viable
populations, each containing at least
1,400 individual plants. The species is
limited to the Neches, Sabine, and
Angelina River basins and the Mud and
Tantabogue Creek basins with 11 extant
sites throughout this range. However,
many of these sites were introduced and
are now compromised by threats from
feral hog damage, hydrological changes,
nonnative and native species
encroachment into habitat, construction
projects, and herbicide overspray.
Future management actions that
ameliorate these threats could allow for
the species to expand within its known
range. The extant populations are
generally small. The only site that has
come close to reaching the conservation
goals are on compartment 55 of the
USFS; however, it still only comprises
53 percent of the needed plants at this
site (750 plants were seen in 2010).
The main sources of habitat loss,
degradation, and modification include
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hydrologic changes (which alter habitat
suitability, growth of plants, expansion
into new areas, and potentially seed
dispersal); encroachment of habitat from
woody natives and invasive nonnatives
(which out-shade and compete for
nutrients and water absorption); road
construction and maintenance projects;
aerial drift of herbicides (which may go
unregulated on private lands); trampling
by feral hogs (known to flatten and
break plants); and herbivory. These can
have a cumulative impact that further
depletes population numbers. Drought
is likely to exacerbate these threats.
Most threats are distributed across the
geographic range of the Neches River
rose-mallow. These threats include:
Encroachment by woody natives and
invasive nonnatives, hydrological
changes, and trampling. The threat from
nonnatives is imminent and is occurring
at all populations, resulting in
competition for light and nutrients, but
maintenance activities occur within
some populations to minimize this
threat. Although information on
populations inhabiting private lands is
a bit lacking, some degree of
hydrological change has been seen at
most sites and is therefore rangewide.
This threat is likely to continue into the
future as water resources become more
scarce and important to the human
population. Drought will likely
exacerbate existing threats and impact
all populations. Direct impacts to plants
from trampling has been documented at
4 of the 11 Neches River rose-mallow
sites, and several others have had
documented observations of damaged
habitat from feral hog tracks. However,
some threats do not affect all Neches
River rose-mallow populations. For
instance, drift from herbicide spraying
likely resulted in the extirpation of the
Neches River rose-mallow in the SH 230
ROW, and the other two populations
within SH ROWs may be affected by
herbicide spraying in the future;
however, Neches River rose-mallow
populations on NF lands are not
threatened by this activity. To our
knowledge, this species has not
experienced a reduction in its range, all
of the known populations and sites are
still present on the landscape, and the
natural populations have maintained
viable population numbers. In addition,
there are four introduced populations
that remain viable, although the
introduced populations on USFS lands
have declined in recent years. Some
threats are likely to occur in the near
future, but are not ongoing. The
potential effects from the construction
of the Lake Columbia reservoir have not
taken place, and there is uncertainty if
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the downstream population of Neches
River rose-mallow would be affected by
changes in hydrology. Therefore, we
conclude that the species does not meet
the definition of an endangered species
(in danger of extinction throughout all
or a significant portion of its range), but
meets the definition of a threatened
species (likely to become an endangered
species in the foreseeable future
throughout all or a significant portion of
its range).
We evaluated whether the Neches
River rose-mallow is in danger of
extinction now (i.e., an endangered
species) or is likely to become in danger
of becoming endangered (i.e., a
threatened species) in the foreseeable
future. The foreseeable future refers to
the extent to which the Secretary can
reasonably rely on predictions about the
future in making determinations about
the conservation status of the species. A
key statutory difference between an
endangered species and a threatened
species is the timing of when a species
may be in danger of extinction, now
(endangered) or in the foreseeable future
(threatened species).
In the case for the Neches River rosemallow, the best available scientific
information indicates that, while
reductions in the species’ range have
not occurred, there have been
significant impacts from habitat
modification and loss that has caused
reductions in most, if not all, of the
known Neches River rose-mallow
populations. However, there are
sufficient numbers of populations
available, some of which are being
conserved for the Neches River rosemallow. Four of the 11 existing Neches
River rose-mallow populations,
including the largest and most robust
population, occur on USFS lands.
However, the USFS Revised Land and
Resource Management Plant does not
address all the significant threats to the
species. The Texas Land Conservancy
private land site was purchased as a
conservation easement for the Neches
River rose-mallow. However, these
protection measures are voluntary. We
conclude that the Neches River rosemallow is likely to become an
endangered species within the
foreseeable future, meeting the standard
of a threatened species.
The Act defines threatened as ‘‘any
species that is likely to become an
endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ A major
part of the analysis of ‘‘significant
portion of the range’’ requires
considering whether the threats to the
Neches River rose-mallow are
geographically concentrated in any way.
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If the threats are consistently uniform
throughout the species’ range, then no
portion is likely to warrant further
consideration.
As threats extend throughout the
species’ entire range and are not
geographically concentrated, it is
unnecessary to determine whether the
Neches River rose-mallow should be
considered an endangered species
within a significant portion of its range.
Therefore, on the basis of the best
available scientific and commercial
information, we are listing the Neches
River rose-mallow as a threatened
species throughout its range in
accordance with sections 3(20) and
4(a)(1) of the Act.
Available Conservation Measures
Conservation measures provided to
species listed as an endangered or
threatened species under the Act
include recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness and conservation by
Federal, State, tribal, and local agencies;
private organizations; and individuals.
The Act encourages cooperation with
the States and requires that recovery
actions be carried out for all listed
species. The protection required by
Federal agencies and the prohibitions
against certain activities are discussed,
in part, below.
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Subsection 4(f) of
the Act requires the Service to develop
and implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse the species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, selfsustaining, and functioning components
of their ecosystems.
Recovery planning includes the
development of a recovery outline
shortly after a species is listed,
preparation of a draft and final recovery
plan, and revisions to the plan as
significant new information becomes
available. The recovery outline guides
the immediate implementation of urgent
recovery actions and describes the
process to be used to develop a recovery
plan. Revisions of the plan may be done
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to address continuing or new threats to
the species, as new substantive
information becomes available. The
recovery plan identifies site-specific
management actions that will achieve
recovery of the species, measurable
criteria that determine when a species
may be downlisted or delisted, and
methods for monitoring recovery
progress. Recovery plans also establish
a framework for agencies to coordinate
their recovery efforts and provide
estimates of the cost of implementing
recovery tasks. Recovery teams
(comprising species experts, Federal
and State agencies, nongovernmental
organizations, and stakeholders) are
often established to develop recovery
plans. When completed, the recovery
outline, draft recovery plan, and the
final recovery plan will be available on
our Web site (https://www.fws.gov/
endangered), or from our Texas Coastal
Ecological Services Field Office in
Corpus Christi (see ADDRESSES, above).
Implementation of recovery actions
generally requires the participation of a
broad range of partners, including other
Federal agencies, States, tribes,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private, State, and tribal lands.
Once these species are listed, funding
for recovery actions will be available
from a variety of sources, including
Federal budgets, State programs, and
cost share grants for non-Federal
landowners, the academic community,
and nongovernmental organizations. In
addition, pursuant to section 6 of the
Act, the State of Texas would be eligible
for Federal funds to implement
management actions that promote the
protection and recovery of the Texas
golden gladecress and the Neches River
rose-mallow. Information on our grant
programs that are available to aid
species recovery can be found at:
https://www.fws.gov/grants.
Please let us know if you are
interested in participating in recovery
efforts for the Texas golden gladecress
and the Neches River rose-mallow.
Additionally, we invite you to submit
any new information on this species
whenever it becomes available and any
information you may have for recovery
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56067
planning purposes (see FOR FURTHER
INFORMATION CONTACT).
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as endangered or
threatened and with respect to its
critical habitat, if any is designated.
Regulations implementing this
interagency cooperation provision of the
Act are codified at 50 CFR part 402.
Section 7(a)(4) of the Act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
listed species or result in destruction or
adverse modification of critical habitat.
If a species is listed subsequently,
section 7(a)(2) of the Act requires
Federal agencies to ensure that activities
they authorize, fund, or carry out are not
likely to jeopardize the continued
existence of the species or destroy or
adversely modify its critical habitat. If a
Federal action may affect a listed
species or its critical habitat, the
responsible Federal agency must enter
into consultation with the Service.
For the Texas golden gladecress,
Federal agency actions that may require
consultation would include federally
funded or permitted actions occurring
within the species’ habitat, specifically
within the zone of Weches outcrops in
Sabine and San Augustine Counties.
Anticipated actions include: (1)
Provision of Federal financial and
technical assistance through the U.S.
Department of Agriculture; (2) permits
issued by the Federal Energy Regulatory
Commission for installation of interstate
natural gas pipelines and associated
infrastructure; (3) provision of Federal
Highway Administration funds for road
projects; (4) provision of Department of
Housing and Urban Development funds
for municipal and residential
construction and infrastructure projects
in towns along SH 21 within the range
of the Texas golden gladecress; (5) funds
for electric service improvements
provided to electric cooperatives by the
U.S. Department of Agriculture’s Rural
Utilities Service; (6) U.S. Army Corps of
Engineers (USACE)-issued section 404
and section 10 permits for wetland
crossings that are part of linear projects
such as roads, transmission lines, or
pipelines; and (7) actions funded by the
Federal Emergency Management
Agency. Also subject to consultation
would be provision of Federal funds to
State and private entities through
Federal programs such as the Service’s
Partners for Fish and Wildlife Program,
State Wildlife Grant Program, and
Federal Aid in Wildlife Restoration
Program.
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For the Neches River rose-mallow,
Federal agency actions that may require
consultation would include federally
funded or permitted actions occurring
within the species habitat. These actions
could include: (1) New construction and
maintenance of roads or highways by
the Federal Highway Administration; (2)
issuance of section 404 Clean Water Act
(33 U.S.C. 1251 et seq.) and section 10
permits by the USACE for federally
funded activities within Federal
jurisdictional wetlands; (3) management
and any other landscape-altering
activities on Federal lands administered
by the Fish and Wildlife Service and
U.S. Department of Agriculture’s USFS;
and (4) Federal Highway Administration
funds given to TXDOT for SH ROW
maintenance.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to endangered and threatened plants.
The prohibitions of section 9(a)(2) of the
Act, codified at 50 CFR 17.61, apply to
endangered plants. These prohibitions,
in part, make it illegal for any person
subject to the jurisdiction of the United
States to import or export, transport in
interstate or foreign commerce in the
course of a commercial activity, sell or
offer for sale in interstate or foreign
commerce, or remove and reduce the
species to possession from areas under
Federal jurisdiction. In addition, for
plants listed as endangered, the Act
prohibits the malicious damage or
destruction on areas under Federal
jurisdiction and the removal, cutting,
digging up, or damaging or destroying of
such plants in knowing violation of any
State law or regulation, including State
criminal trespass law. It is also unlawful
to violate any regulation pertaining to
plant species listed as endangered or
threatened (section 9(a)(2)(E) of the Act).
Chapter 88 of the Texas Parks and
Wildlife Code lists plant species as State
endangered or threatened, with the
same status as the Federal designation,
immediately upon completion of final
Federal listing. The State prohibits
commerce in endangered or threatened
plants and the collection of listed plant
species from public land (defined as
State-owned and land belonging to local
governments) without a permit issued
by TPWD. The State also prohibits
removal for purposes of commercial
sale, possession for commercial sale,
transport for commercial sale, or sale of
all or part of a listed plant from private
land without a permit issued under
Texas Parks and Wildlife Code, section
88.0081. The TPWD requires
commercial permits for the commercial
use of listed plants collected from
private land. Scientific permits are
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required for collection of endangered
plants or plant parts from public lands
for scientific or education purposes.
We may issue permits to carry out
otherwise prohibited activities
involving endangered and threatened
wildlife species under certain
circumstances. Regulations governing
permits are codified at 50 CFR 17.62 for
endangered plants, and at 17.72 for
threatened plants. With regard to
endangered plants, a permit must be
issued for the following purposes: For
scientific purposes or to enhance the
propagation or survival of the species.
It is our policy, as published in the
Federal Register on July 1, 1994 (59 FR
34272), to identify to the maximum
extent practicable at the time a species
is listed, those activities that would or
would not constitute a violation of
section 9 of the Act. The intent of this
policy is to increase public awareness of
the effect of a listing on proposed and
ongoing activities within the range of
listed species. The following activities
could potentially result in a violation of
section 9 of the Act; this list is not
comprehensive:
(1) Unauthorized collecting, handling,
possessing, selling, delivering, carrying,
or transporting of the Texas golden
gladecress or the Neches River rosemallow, including import or export
across State lines and international
boundaries, except for properly
documented antique specimens of these
taxa at least 100 years old, as defined by
section 10(h)(1) of the Act.
(2) Unauthorized removal, damage, or
destruction of Texas golden gladecress
or Neches River rose-mallow plants
from populations located on Stateowned land (highway ROWs) or on land
owned by local governments.
(3) Unauthorized removal, damage, or
destruction of Texas golden gladecress
or Neches River rose-mallow plants on
private land in violation of any State
regulation, including criminal trespass.
(4) Unauthorized removal, damage, or
destruction of Texas golden gladecress
or Neches River rose-mallow plants
from populations located on federally
owned lands.
Questions regarding whether specific
activities would constitute a violation of
section 9 of the Act should be directed
to the Texas Coastal Ecological Services
Field Office in Corpus Christi (see FOR
FURTHER INFORMATION CONTACT).
Requests for copies of the regulations
concerning listed species and general
inquiries regarding prohibitions and
permits may be addressed to the U.S.
Fish and Wildlife Service, Endangered
Species Permits, 6300 Ocean Drive, Unit
5837, Corpus Christi, TX 78412–5837
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(telephone 361–994–9005; facsimile
361–994–8262).
Upon listing the Texas golden
gladecress and the Neches River rosemallow under the Act, the State of
Texas’s Endangered Species Act (Texas
Administrative Code Chapter
88:88.001–88.012) is automatically
invoked. The State’s Endangered
Species Act would prohibit commerce
in endangered or threatened plants and
the collection of listed plant species
from public land without a permit
issued by TPWD and would restrict any
take for commercial purposes from
private land to individuals possessing a
permit issued under section 88.0081.
The State’s law would also encourage
conservation by State government
agencies. Further, the State may enter
into agreements with Federal agencies
to administer and manage any area
required for the conservation,
management, enhancement, or
protection of endangered species. Funds
for these activities could be made
available under section 6 of the Act
(Cooperation with the States). Thus,
some Federal protection afforded to
these species by listing them (Texas
golden gladecress as endangered, and
Neches River rose-mallow as
threatened) will be reinforced and
supplemented by protection under State
law.
Under section 4(d) of the Act, the
Secretary of the Interior has discretion
to issue such regulations as he deems
necessary and advisable to provide for
the conservation of threatened species.
Our implementing regulations (50 CFR
17.71) for threatened plants generally
incorporate the prohibitions of section 9
of the Act for endangered plants, except
under certain circumstances, such as
when a ‘‘special rule’’ promulgated
under section 4(d) of the Act has been
issued with respect to a particular
threatened species. In such a case, the
general prohibitions in 50 CFR 17.61
would not apply to that species, and
instead, the special rule would define
specific take prohibitions and
exceptions, which we consider
necessary and advisable to conserve the
species, that would apply for that
particular threatened species. With
respect to a threatened plant, the
Secretary of the Interior also has the
discretion to prohibit by regulation any
act prohibited by section 9(a)(2) of the
Act. Exercising this discretion, which
has been delegated to the Service by the
Secretary, the Service has developed
general prohibitions that are appropriate
for most threatened plants in 50 CFR
17.71 and exceptions to those
prohibitions in 50 CFR 17.72. We are
not promulgating a special section 4(d)
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Federal Register / Vol. 78, No. 176 / Wednesday, September 11, 2013 / Rules and Regulations
rule, and as a result, all of the section
9 prohibitions, including the ‘‘take’’
prohibitions, will apply to the Neches
River rose-mallow.
References Cited
Required Determinations
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act
(NEPA; 42 U.S.C. 4321 et seq.), need not
be prepared in connection with listing
a species as an endangered or
threatened species under the
Endangered Species Act. We published
a notice outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
Regulation Promulgation
A complete list of references cited in
this rulemaking is available on the
Internet at https://www.regulations.gov at
Docket No. FWS–R2–ES–2012–0064 and
upon request from the Texas Coastal
Ecological Services Field Office in
Corpus Christi (see FOR FURTHER
INFORMATION CONTACT).
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as set forth
below:
Authors
The primary authors of this package
are the staff of the Texas Coastal
Ecological Services Field Office in
Corpus Christi.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 1531–
1544; and 4201–4245, unless otherwise
noted.
2. Amend § 17.12(h) by adding entries
for ‘‘Hibiscus dasycalyx’’ and
‘‘Leavenworthia texana’’ to the List of
Endangered and Threatened Plants in
alphabetical order under ‘‘Flowering
Plants’’, to read as follows:
§ 17.12
*
Endangered and threatened plants.
*
*
(h) * * *
*
Species
Historic range
Scientific name
Family
Status
When listed
Common name
*
Critical
habitat
Special
rules
FLOWERING PLANTS
*
Hibiscus dasycalyx .......
*
*
Neches River rose-mal- U.S.A. (TX) .....
low.
*
Malvaceae ......
*
*
Leavenworthia texana ..
*
Texas golden
gladecress.
*
Brassicaceae ..
*
*
*
*
*
*
*
*
U.S.A. (TX) .....
*
*
T
*
814
17.96(a)
E
*
814
17.96(a)
*
*
Dated: August 29, 2013.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife
Service.
*
[FR Doc. 2013–22085 Filed 9–10–13; 8:45 am]
mstockstill on DSK4VPTVN1PROD with RULES2
BILLING CODE 4310–55–P
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19:08 Sep 10, 2013
Jkt 229001
PO 00000
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*
NA
*
Agencies
[Federal Register Volume 78, Number 176 (Wednesday, September 11, 2013)]
[Rules and Regulations]
[Pages 56025-56069]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-22085]
[[Page 56025]]
Vol. 78
Wednesday,
No. 176
September 11, 2013
Part V
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Determination of
Endangered Status for Texas Golden Gladecress and Threatened Status for
Neches River Rose-Mallow; Final Rule
Federal Register / Vol. 78 , No. 176 / Wednesday, September 11, 2013
/ Rules and Regulations
[[Page 56026]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R2-ES-2012-0064; 4500030113]
RIN 1018-AX74
Endangered and Threatened Wildlife and Plants; Determination of
Endangered Status for Texas Golden Gladecress and Threatened Status for
Neches River Rose-Mallow
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service, determine
Leavenworthia texana (Texas golden gladecress) meets the definition of
an endangered species and Hibiscus dasycalyx (Neches River rose-mallow)
meets the definition of a threatened species under the Endangered
Species Act of 1973, as amended (Act). This final rule adds these
species to the List of Endangered and Threatened Plants and implements
the Federal protections provided by the Act for these species.
DATES: This rule is effective on October 11, 2013.
ADDRESSES: This final rule and other supplementary information are
available on the Internet at https://www.regulations.gov (Docket No.
FWS-R2-ES-2012-0064), https://www.fws.gov/southwest/es/ElectronicLibrary/ElectronicLibrary_Main.cfm, or https://www.fws.gov/southwest/es/ClearLakeTexas/. These documents, as well as all
supporting information are also available for public inspection, by
appointment, during normal business hours at, or by requesting
electronic copies from: U.S. Fish and Wildlife Service, Texas Coastal
Ecological Services Field Office, 6300 Ocean Drive, Unit 5837, Corpus
Christi, TX 78412-5837; by telephone at 361-994-9005; or by facsimile
at 361-994-8262.
FOR FURTHER INFORMATION CONTACT: Edith Erfling, Field Supervisor, U.S.
Fish and Wildlife Service, Texas Coastal Ecological Services Field
Office (see ADDRESSES); by telephone 281-286-8282; or by facsimile 281-
488-5882. Persons who use a telecommunications device for the deaf
(TDD) may call the Federal Information Relay Service (FIRS) at 800-877-
8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. On September 11, 2012 (77 FR 55968),
we published a proposed rule to list Leavenworthia texana (Texas golden
gladecress) as an endangered species and Hibiscus dasycalyx (Neches
River rose-mallow) as a threatened species. In this rule, we are
finalizing our proposed determinations for these species under the Act.
The Act requires that a final rule be published in order to add any
plant species to the List of Endangered and Threatened Plants and to
provide that species protections under the Act. We are publishing a
final rule on the designation of critical habitat for the Texas golden
gladecress and the Neches River rose-mallow under the Act elsewhere in
today's Federal Register. The critical habitat designation final rule
and its supporting documents will publish under Docket No. FWS-R2-ES-
2013-0027, and can also be found at the locations listed in the
ADDRESSES section of this rule.
The basis for our action. Under the Act, a species may be
determined to be endangered or threatened based on any of the following
five factors: (A) The present or threatened destruction, modification,
or curtailment of its habitat or range; (B) overutilization for
commercial, recreational, scientific, or educational purposes; (C)
disease or predation; (D) the inadequacy of existing regulatory
mechanisms; or (E) other natural or manmade factors affecting its
continued existence.
We have determined that the Texas golden gladecress meets the
definition of an endangered species due to the following threats:
In some cases, a total loss of habitat and plants, and in
others a degradation of the herbaceous glade plant communities
supporting the Texas golden gladecress. Activities or factors that
continue to negatively impact the habitat of the Texas golden
gladecress include glauconite quarrying; natural gas and oil
exploration, production, and distribution; invasion of open glades by
nonnative and native shrubs, trees, and vines, and other weedy species;
pine tree plantings in close proximity to occupied glades; herbicide
applications that have potential to kill emerging seedlings; and the
installation of service improvements, including water and sewer lines,
domestic gas lines, or electric lines.
The inadequacy of existing regulatory mechanisms to
protect the Texas golden gladecress or its habitats.
Other natural or manmade factors, including low numbers of
individual plants and few remaining populations.
The above threats are likely exacerbated by climate
change.
We have determined that the Neches River rose-mallow meets the
definition of a threatened species due to the following threats:
Habitat loss and degradation of open habitats on hydric
alluvial soils along sloughs, oxbows, terraces, and wetlands of the
Neches, Sabine, and Angelina River basins and Mud Creek and Tantabogue
Creek basins that support the Neches River rose-mallow. The Neches
River rose-mallow's habitat is being lost and degraded by encroachment
of nonnative and native plant species, particularly trees; herbicide
use; livestock and hog trampling; and alteration of the natural
hydrology associated with seasonal flooding to conditions where habitat
has been drained or has become permanently flooded. Prolonged or
frequent droughts can exacerbate habitat degradation for both species.
Inadequacy of existing regulatory mechanisms to protect
the Neches River rose-mallow or its habitats.
The above threats are likely exacerbated by climate
change.
Peer review and public comment. We sought comments from six
independent specialists to ensure that our designation is based on
scientifically sound data and analyses. We obtained opinions from four
knowledgeable individuals with scientific expertise to review our
technical assumptions and analysis, and to determine whether or not we
had used the best available information. The peer reviewers generally
agreed with portions of our assessment, including the threats analysis,
and most of our conclusions, although they pointed out areas where
additional research would refine our understanding of the two species'
habitat requirements and range. The peer reviewers pointed out
additional information, clarifications, and suggestions for future
research that would inform future surveys to refine the geographic
range, and help with management and recovery efforts. Information we
received from peer review is incorporated in this final revised
designation. We also considered all comments and information we
received from the public during the comment periods.
Previous Federal Actions
On September 11, 2012 (77 FR 55968), we published a proposed rule
to list the Texas golden gladecress as endangered and the Neches River
rose-mallow as threatened, both with critical habitat. On April 16,
2013 (78 FR 22506), we reopened public comment period on the
[[Page 56027]]
proposed rule. On May 1, 2013, we held a public hearing to accept oral
and written comments on the proposals.
We are publishing a final rule on the designation of critical
habitat under the Act (16 U.S.C. 1531 et seq.) for the Texas golden
gladecress and the Neches River rose-mallow elsewhere in today's
Federal Register.
Background
Species Information
It is our intent to discuss below only those topics directly
relevant to the listing of the Texas golden gladecress as endangered,
and the Neches River rose-mallow as threatened, in this final rule.
Species information for the Texas golden gladecress and Neches River
rose-mallow can also be found in the September 11, 2012 (77 FR 55968),
proposed rule.
Texas Golden Gladecress
Taxonomy and Description
Texas golden gladecress is a small, annual, herbaceous plant
belonging to the mustard family (Brassicaceae). Dr. M. C. Leavenworth,
an Army physician, first collected the taxon in Choctaw County,
Oklahoma, in 1835, and the specimens were later described as a new
species, Leavenworthia aurea, by Torrey (Mahler 1981, pp. 76-77).
From 1836 to 1837, Leavenworth collected similar specimens near the
present-day town of San Augustine, San Augustine County, Texas, and
these were also identified as L. aurea. E. J. Palmer (1915 and 1918),
and D. S. and H. B. Correll (1961 to 1962) as cited by Mahler (1981,
pp. 83) made later collections of the plant in the San Augustine area.
George and Nixon (1990, pp. 117-127) studied and mapped populations in
this area between 1979 and 1980. W. H. Mahler studied the collected
specimens and their habitat, and described the Texas plants as a new
species, Leavenworthia texana (Mahler 1987, pp. 239-242), based on
differences in morphological characteristics of flowers and leaves, and
in chromosome number, between the Oklahoma and Texas plants (Mahler
1987, pp. 239-242).
According to Mahler (1987, p. 240), Texas golden gladecress flower
petals were a brighter, deeper yellow than those of L. aurea, and the
petals were egg-shaped and flat instead of being broad and notched. The
L. texana had wider-than-long terminal leaf segments that were usually
distinctly lobed while L. aurea's terminal leaves were essentially
unlobed, flat, and more circular. Texas plants had a chromosome number
of 2n = 22 (Nixon 1987, pers. comm. in Mahler 1987, pp. 239, 241) while
the Oklahoma L. aurea had 2n = 48 (Rollins 1963, pp. 9-11; Beck et al.
2006, p. 156). We are aware that a recently completed monograph of the
genus may have taxonomic implications for the Texas and Oklahoma
Leavenworthia species in the future, but several questions, including
the differences in chromosome number, remain unresolved and no
supporting information that would change the current status of Texas
golden gladecress has been published to date (Poole 2011a, pers.
comm.).
Texas golden gladecress is a weakly rooted, glabrous (smooth,
glossy), winter annual (completes its life cycle in 1 year). Texas
golden gladecress is small in stature, less than 3.9 inches (in) (10
centimeters (cm)) in height, making it difficult to find except during
flowering or when it bears fruit. The leaves are 0.8-3.1 in (2-8 cm)
long and 0.4-0.6 in (1-1.5 millimeters (mm)) wide, forming rosettes at
the base of the plant. Terminal leaf segments are wider-than-long, and
usually distinctly lobed, with angular teeth. Flowers are bright yellow
and borne on scapes (leafless flowering stems or stalks arising from
the ground) that are 1.2-3.5 in (3-9 cm) long early in the flowering
season. Later in the season, the flowers occur on unbranched flower
clusters that come off a single central stem from which the individual
flowers grow on small stalks, at intervals. The four petals are bright
golden-yellow with a slightly darker base, narrowly obovate (tongue-
shaped), 0.3-0.4 in (7-10 mm) long and 0.1-0.2 (3.5-5 mm) wide. The
fruit is a slender seed capsule, known as a silique, with a length
(0.6-1.2 in (15-30 mm)) that is more than twice its width (0.08-0.22 in
(2-5.5 mm)) and that contains 5 to 11 flattened, circular or
spherically shaped seeds. The description above was drawn from Poole et
al. (2007, p. 286), who adapted it from others.
Habitat
Texas golden gladecress occurs within the Pineywoods natural region
of easternmost Texas, within the Gulf Coastal Plain Physiographic
Region. The region is defined by uplands that are forested by pine
dominated woodlands, interspersed with bottomland, mesic slope, and
bald cypress-tupelo swamp forests. Water oak and willow oak are
prominent in the large stream floodplains, while some ancient sloughs
are fringed by planer tree and overcup oaks (Dolezel 2012, pers.
comm.). Many of the rare plants of the Pineywoods region, including the
Texas golden gladecress and the federally endangered Lesquerella
pallida (=Physaria pallida) (white bladderpod) are found in small-scale
plant communities tied to ``geologic and hydrologic conditions that are
themselves rather rare on the landscape'' (Poole et al. 2007, p. 6).
Based on all documented occurrence records, the Texas golden
gladecress is endemic to glade habitats in northern San Augustine and
northwest Sabine Counties, Texas, where it is a habitat specialist,
occurring only on outcrops of the Weches Geologic Formation (Mahler
1987, p. 240; George and Nixon 1990, p. 120; Poole et al. 2007, pp.
286-287). The gladecress grows only in glades on shallow, calcium-rich
soils that are wet in winter and spring. These occur on ironstone
(glauconite or green-stone) outcrops (Poole et al. 2007, p. 286).
All species within the small genus Leavenworthia share an
adaptation to glade habitats that have unique physical characteristics,
the most important being a combination of shallow soil depth and high
calcium content (dolomitic limestone or otherwise calcareous soils)
where the soil layers have been deposited in such a manner that they
maintain temporary high-moisture content at or very near the surface
(Rollins 1963, pp. 4-6). Typically, only a few inches of soil overlie
the bedrock, or, in spots, the soil may be almost lacking and the
surface barren. Within the Weches Formation glades, gladecress habitat
occurs on thin soils that overlie calcium-rich parent materials where
the calcium is derived from a myriad of fossilized, calcium-dominated
oyster shells and other marine life (Dolezel 2012, pers. comm., p. 1).
The glade habitats that support all Leavenworthia species are
extremely wet during the late winter and early spring and then dry to
the point of being parched in summer (Rollins 1963, p. 5). These glades
can vary in size from as small as a few meters to larger than 0.37
square miles (mi\2\) (1 square kilometer (km\2\)) and are characterized
as having an open, sunny aspect (lacking canopy) (Quarterman 1950, p.
1; Rollins 1963, p. 5). The landscape position of the glades may also
play a role in assuring the cyclic moisture regime required by glade
vegetation communities.
The Weches Geologic Formation consists of Eocene-age deposits that
lie mostly in an east-west band of ancient marine sediments. These
sediments were deposited in a line roughly parallel to the Gulf of
Mexico, running from Sabine to Frio Counties, Texas. The Weches
Formation also extends over 100 miles to the north of Nacogdoches
County into Smith, Wood, Upshur, Marion, and Cass Counties, Texas, and
even into Miller County, Arkansas
[[Page 56028]]
(Godwin 2012, pers. comm., p. 2). A layer of glauconite clay is either
exposed at the surface or covered by a thin layer of calcareous
(calcium-containing) sediment measuring as deep as 20 in (50 cm)
(George and Nixon 1990, pp. 117-118). Glauconite is a characteristic
mineral of marine depositional environments, presenting a greenish
color when initially exposed to the atmosphere, and later turning red
(Davis 1966, pp. 17-18; Nemec 1996, p. 7). The area of the Weches
outcrops in San Augustine County is referred to as the ``redlands''
(Ritter 2011b, pers. comm.). The glauconite is very friable (crumbly)
and has low resistance to weathering (Geocaching.com 2010, p. 5). The
soils overlying the clay layer are typically rocky and shallow (George
1987, p. 3) and at all Texas golden gladecress sites are classified
within the Nacogdoches, Trawick, or Bub soils series (United States
Department of Agriculture 2009, entire).
Within the known range of the Texas golden gladecress, Weches
outcrops occur in a band averaging 5 miles (mi) (8 kilometers (km)) in
width that parallels Texas State Highway (SH) 21 through northern San
Augustine and northwestern Sabine Counties (Sellards et al. 1932 in
Diggs et al. 2006, p. 56). It has been deeply dissected by erosion that
created islands of thin, loamy, alkaline soils (pH 7-8), within the
normally deep, sandy, acidic soils (pH 4-5) of the Pineywoods region.
The glauconite layer of the Weches Formation is fairly impermeable to
water, producing saturated, thin upper soils in late fall through
spring, that dry out and harden during summer months (George 1987, pp.
2-4; Bezanson 2000 in Diggs et al. 2006, p. 56). Down-slope seepage
across the Weches terraces may also be important to maintain the
hydrology required by the gladecress (Singhurst 2003, pers. comm.). The
cyclic moisture regime and the alkalinity of the soils produce
conditions unique to the Weches outcrops. Certain plants, such as the
Texas golden gladecress, have evolved to live within these specialized
geologic formations (Mahler 1987, p. 240; George and Nixon 1990, pp.
120-122).
Biology
The Texas golden gladecress occurs in open, sunny, herbaceous-
dominated plant communities in Weches glades, in some areas that also
support the white bladderpod (Bridges 1988, pp. II-7, II-35, and II-35
supplement). Unlike the white bladderpod, which can grow throughout the
glade, the gladecress is restricted to the outcrop rock faces within
the glades where it occurs (Nemec 1996, p. 8).
As is true of other Leavenworthia species (Rollins 1963, p. 6),
Texas golden gladecress seeds germinate during fall rains and the
plants overwinter as small, tap-rooted rosettes. Flowering begins in
February and continues into March, and sometimes as late as April,
depending on annual weather conditions. Rollins (1963, p. 6) noted that
the blooming period of Leavenworthia varied according to the
temperature, moisture, and severity of winter freezes. Fruit production
is generally seen from March into April. The plants respond to drying
of the soil by dropping seed and withering away, usually in April and
May (Singhurst 2011b, pers. comm.). By summer months, gladecress plants
are dead, replaced by other low-growing species such as Sedum
pulchellum (stonecrop), Portulaca oleracea (common purslane),
Phemeranthus parviflorus (sunbright), and Eleocharis occulata
(limestone spikerush) (Singhurst 2012e, pers. comm.). Although seed
dispersal has not been studied in Texas golden gladecress, observations
indicate that seeds fall within 6-8 in (15-20 cm) of the parent plant
(Singhurst 2011c, pers. comm.).
Little is known about the Texas golden gladecress's seed bank as
this aspect of life history has not been researched. The species did
reappear at two sites where it was believed lost due to habitat
degradation. A population location, the Geneva Site in Sabine County,
was bulldozed in late March 1999, one week after flowering plants were
counted; the site was subsequently described by the surveyor as ``lost
or destroyed'' (Turner 1999, pers. comm.). However, plants were found
again at this site in 2003, and continued to emerge in succeeding
years. At a second site in San Augustine County (Chapel Hill Site) a
thick growth of the invasive, nonnative shrub, Rosa bracteata
(Macartney rose) was removed in 1995. Post-brush removal, the Texas
golden gladecress reappeared after not having been seen for the
previous 10 years (Nemec 1996, p. 1). The species' reappearance after
these habitat alterations suggests a persistent seed bank, although
there have been no formal studies to verify this hypothesis.
Rare plants often have adaptations such as early blooming, extended
flowering, or mixed-mating systems that allow them to persist in small
populations (Brigham 2003, p. 61). The Texas golden gladecress is
believed to be self-compatible and able to self-fertilize (Rollins
1963, p. 19; Beck et al. 2006, p. 153). The species may have evolved
for self-fertilization when conditions are not favorable for insect-
vectored pollination, lessening the species' dependence on pollinators
for cross-pollination and survival and potentially making the species
more resilient under conditions of small, geographically separated
populations. Rollins (1963, pp. 41-47) speculated that species in the
genus Leavenworthia evolved from a self-incompatible original ancestor
to self-compatibility in some species to persist with a diminishing
overlap in seasonality of adequate moisture in glade habitats versus
availability of insect pollinators (e.g., as the southeastern part of
the United States warmed, the required moisture levels for germination
and flowering became more restricted to winter months when insect
availability was lower). This could help to enhance the species'
persistence, at least in the short term, in a fragmented landscape
where habitat patches may be so distant from one another as to preclude
pollinators' movements between them. Even so, the presence of other
flowering plants at gladecress sites could help to attract and maintain
a reservoir of potential pollinators, thereby increasing the chances
for the gladecress to be cross-pollinated. This would benefit the
species by potentially providing, or maintaining, a higher level of
genetic diversity.
Distribution and Status
Texas golden gladecress is known from eight locations (historic and
extant), including one introduced population, all within a narrow zone
that parallels SH 21 in San Augustine, Sabine, and Nacogdoches Counties
(Texas Natural Diversity Database (TXNDD) 2012b). Table 1 (below)
summarizes the location information for Texas golden gladecress
populations (taken from the TXNDD 2012b). Based on known population
locations, taken from the TXNDD element occurrence records from 1974-
1988, the Weches glades of San Augustine County appear to be the center
of the species' distribution; to date all but one of the naturally
occurring populations were found in this area, with the other naturally
occurring population in Sabine County. One population was successfully
introduced into Nacogdoches County. All locations (historic and extant)
occur primarily on privately owned land, although the plants do extend
onto the Texas Department of Transportation (TXDOT) right-of-way (ROW)
at two sites: Geneva Site and Caney Creek Glade Site 1.
[[Page 56029]]
Table 1--Location and Status of Texas Golden Gladecress Populations
----------------------------------------------------------------------------------------------------------------
Population Historic site
County designation Status description Land owner
----------------------------------------------------------------------------------------------------------------
San Augustine.............. Caney Creek Extant.......... By 2001, was Private & State ROW.
Glade Site 1. less than 100
ft[sup2] (9
m[sup2]).
San Augustine.............. Chapel Hill Extant.......... Tract on which Private.
(also known as Texas golden
Tiger Creek). gladecress was
found was less
than 0.25 ac
(0.1 ha).
Sabine..................... Geneva.......... Extant.......... Size of site Private & State ROW.
was ~ 100
ft[sup2] (9
m[sup2]).
Nacogdoches................ Simpson Farms Extant through Population ~ Private.
(introduced 2009. Site was 200 ft[sup2]
population). eradicated by (18 m[sup2])
pipeline in in size.
2011.
San Augustine.............. Caney Creek Status unknown. Small Private.
Glade Site 7. Possibly population;
extant--not locally
accessible in abundant in
last 24 years. very small
area.
San Augustine.............. Caney Creek Site is now Site was ~ 3 ac Private.
Glade Site 2. excavated pits. (1.21 ha).
San Augustine.............. Caney Creek Site is now Multiple tracts Private.
Glade Site 6. excavated pits. totaling ~ 10
Possibility ac. Sites 6,
that some 7, and 8 in
habitat and different
plants remain areas on these
on adjacent, tracts. Site 6
unquarried land. was the
largest known
population
(thousands of
plants).
San Augustine.............. Caney Creek Site lost to Very small Private.
Glade Site 8. excavated pits. population on
a degraded
outcrop.
----------------------------------------------------------------------------------------------------------------
Four Texas golden gladecress populations (Caney Creek Glade 1,
Chapel Hill, Geneva, and Simpson Farms) were present through 2009, the
last year that the plants were surveyed and counted (Singhurst 2011a,
pers. comm.). In October 2011, Service and Texas Parks and Wildlife
Department (TPWD) biologists visited all four known locations and found
that the plants and habitat at the introduced site in Nacogdoches
County (Simpson Farms) had been removed by a recent pipeline
installation. The habitat was still intact at the other three locations
in October 2011 (Cobb 2011, pers. comm.), and the presence of the
plants themselves was subsequently observed at the three accessible
sites in February 2012 (Singhurst 2012f, p. 1).
Three San Augustine County occurrences (Caney Creek Glade Sites 2,
6, and 8) were believed extirpated, at least in large part, by
construction of glauconite mines (open pits) beginning in the late
1990s. These occurrences may have been part of a much larger glade
complex, referred to as the Caney Creek Glade Complex, that included
the Caney Creek Glade Sites 1, 2, 6, 7, and 8. These five occurrences
were located within an area extending out to 1.5 mi (2.41 km) to the
east of the town of San Augustine (TXNDD 2012b, unpaginated). In 1987,
the Caney Creek Glade Site 6 was described as having Texas golden
gladecress plants ``in the thousands'' (TXNDD 2012b, unpaginated).
Access to these three privately owned sites is prohibited; therefore,
we cannot ascertain whether any plants or their habitat are still
present on the peripheries of the mined areas.
For Caney Creek Glade Site 7, the last TXNDD (2012b, unpaginated)
element of occurrence record was from 1988, a time when the presence of
Texas golden gladecress was confirmed at the site. The site was visited
by a forestry consultant in 1996, who described the glade as being
intact at that time. This individual revisited the site in 2000, and
found invasive woody plants encroaching into the glade (Walker 2012, p.
4). There were no further site visits due to lack of access to this
privately owned tract. Satellite images taken as recently as 2008 show
this site has not been altered by construction or quarrying (mining),
but the open glade appearance at this site has changed to one of dense
growth of woody vegetation, so it is unknown whether the plants still
occur at the site.
Table 2 presents estimates for extant Texas golden gladecress
populations between 1999 and 2009 (Service 2010a, p. 4). The total
number of plants seen in 2009 was 1,108. The largest population,
consisting of 721 plants, was at the introduced site in Nacogdoches
County, a site that was lost in 2011, when a pipeline route was
constructed through it. This represents a loss of 65 percent of the
known plants. After 2009, approximately 400 plants in three populations
were all that remained of this species. The number of Texas golden
gladecress plants fluctuated widely from year to year, likely due to
differences in precipitation levels between years. The Texas golden
gladecress is dependent on fall and winter rain to saturate the
sediment and produce the seeps and pooling it requires, and drought
conditions were noted to have a significant negative effect on
reproduction (Turner 2000, p. 1) as seen in the drought years of 1999-
2000 (Texas Water Resources Institute 2011, unpaginated) when the
Chapel Hill site decreased from 91 to 67 plants and the Caney Creek
Glade Site 1 decreased from 490 to 96 plants (Service 2010a, p. 5).
Table 2--Population Estimates for Texas Golden Gladecress At Monitored
Sites
------------------------------------------------------------------------
Caney
Year Chapel Creek Geneva Simpson
Hill Glade 1 Farms
------------------------------------------------------------------------
1999............................ 91 490 319 *NS
2000............................ 67 96 NS NS
2001............................ 96 520 NS 270
[[Page 56030]]
2002............................ NS NS NS NS
2003............................ 42 NS 57 57
2004............................ NS NS NS NS
2005............................ 40-50 0 54 2,873
2006............................ NS NS 200 NS
2007............................ 200 NS 1,000 1,000
2008............................ 9 NS 49 NS
2009............................ 98 29 260 721
------------------------------------------------------------------------
* NS--Not surveyed.
Singhurst (2011a, pers. comm.) referred to the difficulty of trying
to determine population trends for the Texas golden gladecress due to
the lack of comprehensive numbers for the species. He attributed this
data gap to variation in surveyors and their techniques, the inability
to see Texas golden gladecress plants under invasive brush, lack of
access to multiple sites, and the fluctuation in plant numbers
associated with moisture conditions. Nevertheless, despite these
limitations, it is evident that there are few remaining populations and
that the overall numbers of existing plants are fluctuating. For
example, a decrease in plant numbers in 2009 (Singhurst 2009, p. 1) was
likely due to drought; however, following significant rains in late
fall 2011 and early winter 2012, Singhurst (2012f, pers. comm.) noted
higher numbers of plants than the 2009 counts at Geneva, Chapel Hill,
and Caney Creek Glade Site 1.
Most of the known populations, historic and extant, were and are
restricted to small areas (see Table 1). For example, in San Augustine
County, the Chapel Hill site is less than 0.2 acres (ac) (0.1 hectare
(ha)) in size and lies between a pasture fence and gravel road
southwest of SH 21. The area of the plants at the Caney Creek Glade
Site 1 is less than 100 feet squared (ft\2\) (9 meters squared (m\2\))
in size, on the side of Sunrise Road south of SH 21. In Sabine County,
the plants at the Geneva site occupy approximately 100 ft\2\ (9 m\2\)
adjacent to, and west of, SH 21, south of Geneva. The total area
occupied by the plants at the remaining three sites covers less than
1.2 ac (0.5 ha). Area sizes for Texas golden gladecress occurrences
were taken from the TXNDD element of occurrence records.
Although no new populations of Texas golden gladecress have been
found since the late 1980s, there is potential for more Texas golden
gladecress to exist across the Weches glades region. Known populations
all occur close to roads, suggesting that most searches for the species
were nearby to public road access. All known occurrences are on private
property, as is all remaining habitat, and surveys cannot be conducted
without landowner permission. Effective identification of suitable
habitat is needed to survey for new populations. Even in areas of
potential Weches glades, as identified using Geographic Systems
Information (GIS) data, including aerial, geologic, and hydrologic data
sources, the habitat may not contain Texas golden gladecress
populations. Between 1999 and 2003, The Nature Conservancy (TNC) used
these tools to identify 44 potential sites of Texas golden gladecress
and white bladderpod occurrence in the San Augustine glades. The San
Augustine glades were delineated by TNC as a subset of the Weches
glades for purposes of developing an area conservation plan. The San
Augustine glades are located in north-central and northeastern San
Augustine County. TNC was granted access to 14 of the 44 sites, but
found little Weches glade habitat, and no new Texas golden gladecress
or white bladderpod sites (Turner 2003, in Service 2010a, p. 3).
Conservation
The Texas golden gladecress was included as a nested element within
the Coastal Plain Carbonate Glades conservation element of the San
Augustine Glades Area Conservation Plan developed by TNC of Texas in
2003 (TNC 2003, entire). This plan was envisioned to provide guidance
for the conservation and restoration of a network of ecologically
functional forests and glades along the Weches Geological Formation in
San Augustine County. The plan was generated through TNC's structured
conservation planning process, which relied on a science team with
expertise in east Texas flora and habitats, including members from
academia, botanical institutions, and Federal and State agencies. The
conservation planning process concluded that at least 8 viable (self-
sustaining, ecologically functioning) populations of Texas golden
gladecress, containing an average of 500 individual plants each, at
least 1 out of every 5 years, was the target conservation goal for the
species (TNC 2003, pp. 8, 12).
Neches River Rose-Mallow
Taxonomy and Description
Hibiscus dasycalyx (Neches River rose-mallow) (Blake and Shiller)
is a nonwoody perennial (plant that grows year after year) in the
Malvaceae (mallow) family that grows 1.9-7.5 feet (ft) (0.6-2.3 meters
(m)) tall (Correll and Johnston 1979, p. 1030). Leaves are alternate
and simple, generally t-shaped and deeply three-lobed with petioles
(leaf stalks) 1.1-1.9 in (3-5 cm) long (Correll and Johnston 1979, p.
1030). The Neches River rose-mallow generally produces a single creamy
white (rarely pink) flower at the base of the leaf stalks along the
uppermost branches or stems (Blanchard 1976, pp. 27-28; Warnock 1995,
p. 2; Poole et al. 2007, pp. 264-265). Because the plants are single to
multi-stemmed and each branch or stem can have numerous leaves, the
total number of flowers per plant can number in the hundreds (Poole
2013b, pers. comm.). Flowering occurs between June and August (Poole et
al. 2007, p. 265), sometimes into late October depending on water
availability during springtime inundations (Warnock 1995, p. 20; Center
for Plant Conservation 2011). Large and numerous stamens are
monodelphous, forming a tube that is united with the base of the petals
(Klips 1999, p. 270).
The Neches River rose-mallow was first collected by Ivan Shiller on
June 23, 1955, at the type locality at SH 94 (also referred to as Apple
Springs), Trinity County, Texas, and it was later recognized it as a
distinct species (Correll and Johnston 1979, pp. 1030-1031). Blake
(1958, p. 277) determined that the Neches River rose-mallow was
different from the closely related
[[Page 56031]]
Hibiscus laevis (halberdleaf rose-mallow) by examining specimens from
the type locality. Gould (1975), Nixon (1985), Hatch et al. (1990),
Johnston (1990), and Fryxell (all in Warnock 1995, pp. 1-2; Poole 2002,
pers. comm.) all recognized the Neches River rose-mallow as a distinct
species.
Two similar-looking Hibiscus species, H. laevis (halberdleaf rose-
mallow) and H. moscheutos (crimsoneyed or wooly rose-mallow) are
wetland species documented in areas where the Neches River rose-mallow
occurs. All three of these species have a similar general appearance,
but can be separated based on a comparison of external characteristics
including leaf structure, and degree of pubescence (fine hairs) on the
calyx, leaves, capsule (dry fruit), or seeds (Correll and Correll 1975,
p. 1118; Blanchard 1976, p. 5; Warnock 1995, p. 4). Similar to H.
moscheutos, the Neches River rose-mallow has a hairy calyx but with
larger, spreading hairs rather than a covering of small, short hairs
(Warnock 1995, pp. 2-3). Geographically, these three species can be
found within similar habitats, but the halberdleaf and the crimsoneyed
rose-mallows prefer areas near deeper water and are found along edges
of major rivers and streams (Blanchard 1976, pp. 10-14; Poole 2011b,
pers. comm.), compared with the Neches River rose-mallow, which is
found in side channels and floodplains of major river drainages. Based
on the best scientific and commercial data available on the species'
morphology, biology, and habitat-specific needs, we conclude that the
Neches River rose-mallow is a valid taxon.
Habitat
The Neches River rose-mallow is endemic to the relatively open
habitat (Kennedy and Poole 1990, p. 11) of the Pineywoods (or Timber
belt) of east Texas (Gould 1975, p. 1; Correll and Johnston 1979, p.
1030), within Cherokee, Houston, Harrison, and Trinity Counties, and
has been introduced into Nacogdoches and Houston Counties. Shortleaf-
loblolly pine-hardwood forests, longleaf pine (Pinus palustris), and
loblolly pine forest (Pinus taeda) dominate the Pineywoods vegetation
region (Telfair 1983, p. 29; Diggs et al. 2006, p. 6). More
specifically, Neches River rose-mallow is found within seasonally
flooded river floodplains as described by Diggs et al. (2006), where
the natural bottomlands occupy flat, broad portions of the floodplains
of major rivers and are seasonally inundated. Loamy to clayey soils
seasonally flood and host flood-tolerant species of Quercus sp. (oak),
Liquidambar styraciflua (sweetgum), Ulmus americana (American elm),
Nyssa biflora (swamp tupelo), and Acer rubrum (red maple) (Diggs et al.
2006, p. 103). Bottomland and floodplain areas may be dominated by Q.
lyrata (overcup oak). Stands of shortleaf, longleaf, and loblolly pine
are not occupied by the Neches River rose-mallow. The common native
woody and herbaceous plant associates are listed in Table 3 (Warnock
1995, pp. 14-15; Poole et. al 2007, pp. 264-265).
Table 3--Native Plant Associates of Neches River Rose-Mallow
------------------------------------------------------------------------
Scientific name Common name
------------------------------------------------------------------------
Native Woody Plant Associates
------------------------------------------------------------------------
Carya aquatica......................... water hickory.
Cephalanthus occidentalis.............. common buttonbush.
Celtis laevigata var. laevigata........ sugar berry.
Fraxinus sp............................ ash.
Quercus lyrata......................... overcup oak.
Q. nigra............................... wateroak.
Liquidambar styraciflua................ sweetgum.
Salix nigra............................ black willow.
------------------------------------------------------------------------
Native Herbaceous Plant Associates
------------------------------------------------------------------------
Boehmeria cylindrica................... smallspike false nettle.
Brunnichia ovata....................... buckwheat vine.
Carex lupulina......................... common hop sedge.
Chasmanthium sessilifolium............. longleaf woodoats.
Diodia virginiana...................... Virginia buttonweed.
Eichhornia crassipes................... water hyacinth.
Heliotropium indicum................... Indian heliotrope.
Hibiscus moscheutos.................... crimsoneyed rose-mallow.
H. moscheutos.......................... wooly rose-mallow.
H. laevis (= H. militaris)............. halberdleaf rose-mallow.
Hydrolea ovata......................... ovate false fiddleleaf.
Hydrocotyle ranunculoides.............. floating pennywort.
Juncus effusus......................... common rush.
Ludwigia leptocarpa.................... anglestem primrose-willow.
Nuphar lutea........................... yellow pond-lily.
Phanopyrum gymnocarpon................. Savannah-panicgrass.
Panicum rigidulum...................... redtop panicgrass.
Pluchea foetida........................ stinking camphorweed.
Polygonum hydropiperoides.............. swamp smartweed.
Pontederia cordata..................... pickerelweed.
Rhynchospora corniculata............... shortbristle horned beaksedge.
Sesbania herbacea...................... bigpod sesbania.
Scirpus cyperinus...................... woolgrass.
Thalia dealbata........................ powdery alligator-flag.
Trachelospermum difforme............... climbing dogbane.
------------------------------------------------------------------------
[[Page 56032]]
Sites where the Neches River rose-mallow has been found have been
described as sloughs, oxbows, terraces, and sand bars. Sites are
seasonally inundated or regularly flooded bottomlands (Diggs et al.
2006, p. 103) that include low areas (Warnock 1995, p. 13) within the
Neches, Sabine, and Angelina River basins and Mud and Tantabogue Creek
basins. Soils are classified generically as hydric alluvials (water-
saturated soils) of the Inceptisol or Entisol orders (Diggs et al.
2006, pp. 46, 79) and although generally water-saturated, can often be
surficially dry. The U.S. Department of Agriculture's (USDA) Natural
Resources Conservation Service (NRCS) completed soils surveys for all
counties with known occurrences of the Neches River rose-mallow, and
the associated soils are frequently flooded clay loams. Sites are both
perennial and intermittent wetlands with water levels between sites
varying due to their proximity to water, amount of rainfall, and
floodwaters. Intermittent wetlands are inundated during the winter
months but become dry during the summer months (Warnock 1995, p. 11).
Warnock (1995) noted that seed dispersal is likely by water, and Scott
(1997, p. 5) also stated that seed dispersal appears to be entirely
water dependent. While water-mediated seed dispersal of the Neches
River rose-mallow is highly likely, it is not known that flowing water
is required for downstream dispersal of rose-mallow seeds. Rivers of
east Texas tend to overflow onto banks and floodplains (Diggs et al.
2006, p. 78), especially during the rainy season, thereby dispersing
seed. Research has not been done to identify methods of seed dispersal
upstream; however, avian species may facilitate this process.
Biology
The Neches River rose-mallow is a perennial that dies back to the
ground every year and resprouts from the base; however, the plant still
maintains aboveground stems. Longevity of the species is unknown, but
it may be long-lived. Cross-pollination occurs (Blanchard 1976, p. 38)
within the Neches River rose-mallow populations, and the species has
high reproductive potential (fecundity). The number of flowers and
fruits per plant were documented during the TPWD's annual monitoring of
the Neches River rose-mallow along SH ROWs. The species produced an
average of 50 fruits per plant, but seed viability and survivorship are
not known (Poole 2012a, pers. comm.). An open canopy is typical within
Neches River rose-mallow habitat (Warnock 1995, pp. 11, 13), but plants
also grow in partial sun (as is the case at SH 204). Sunlight is needed
for blooming, as the blooming period may only last 1 day (Snow and
Spira 1993, p. 160).
Potential pollinators of the Neches River rose-mallow may include,
but are not limited to, the common bumblebee (Bombus pensylvanicus),
Hibiscus bee (Ptilothrix bombiformis), moths, and the scentless plant
bug Niesthrea louisianica (Klips 1995, p. 1471; Warnock 1995, p. 20;
Warriner 2011, pers. comm.). Both Hibiscus laevis and H. moscheutos are
pollinated by common bumblebees and the Hibiscus bee (Snow and Spira
1993, p. 160; Klips 1999, p. 270). The solitary Hibiscus bee prefers
gently sloping or flat areas with sandy or sandy-loam soils for nesting
areas (Vaughan et al. 2007, pp. 25-26; Black et al. 2009, p. 12), and
female bees will excavate nest cavities in elevated, hard packed dirt
roadways or levees near stands of Hibiscus (in this case H. palustris)
and standing water (Rust 1980, p. 427). Members of the genus Bombus
(family Apidae) are social bees, predominantly found in temperate
zones, nesting underground (Evans et al. 2008, p. 6) in sandy soils
(Cane 1991, p. 407). Bumblebees nest in small cavities, often
underground in abandoned rodent nests, in grass (Black et al. 2009, p.
12), or in open, grassy habitat (Warriner 2012a, pers. comm.). Other
aboveground-nesting bees that may potentially pollinate the Neches
River rose-mallow may include carpenter, mason, and leaf cutter bees
that nest in dead snags or twigs or standing dead wood (Warriner 2012a,
pers. comm.). Maximum foraging distances of solitary and social bee
species are 492 to 1,968 ft (150 to 600 m) (Gathmann and Tscharntke
2002, p. 762) and 263 to 5,413 ft (80 to 1,650 m) (Walther-Hellwig and
Frankl 2000, p. 244), respectively. The scentless plant bug is a member
of the Rhopalidae family found specifically in association with various
members of the Malvaceae family. This species is known to deposit eggs
on both the vegetative and reproductive parts of mallow plants (Spencer
1988, p. 421). Holes have been eaten in floral parts of Neches River
rose-mallow plants, suggesting that the scentless plant bug may be a
pollinator as well as a consumer of the Neches River rose-mallow.
Natural fires occurred every 1 to 3 years in east Texas (Landers et
al. 1990, p. 136; Landers 1991, p. 73) and controlled the overgrowth of
longleaf and loblolly pine, as well as nonnative species. In more
recent history, humans used fire to suppress overgrowth. Fire
suppression allows for sweetgum, oaks, Carya sp. (hickories), Diospyros
virginiana (common persimmon), and Magnolia grandiflora (southern
magnolia) to invade the natural pine forests (Daubenmire 1990, p. 341;
Gilliam and Platt 1999, p. 22), and reduce the open canopy needed by
the Neches River rose-mallow. Lack of fire increases the opportunity
for nonnative species, such as Triadica sebifera (Chinese tallow), to
invade these sites.
Distribution and Status
The natural geographic range of the Neches River rose-mallow is
within Trinity, Houston, Harrison, and Cherokee Counties, Texas, on SH
ROWs and on private and Federal lands. However, the species has been
introduced outside of the known geographic range in Nacogdoches County
on private land (Mill Creek). In addition, populations of Neches River
rose-mallow have been introduced within their natural geographic range
on Federal lands in Houston County. In total, there are 12 occurrences
of Neches River rose-mallow (see Table 4). However, only 11 of these
are within the known geographic range and, as of October 2011, are
considered occupied by the Neches River rose-mallow. The Neches River
rose-mallow plants within the SH 230 ROW have not been seen since 2002,
and the site was considered extirpated. In 2011, Neches River rose-
mallow plants were not located at this site, but in 2012, a graduate
student from Stephen F. Austin State University reported seeing the
Neches River rose-mallow along SH 230 in the ROW somewhere near the
former site (Melinchuk 2012, p. 3).
[[Page 56033]]
Table 4--Population Estimates for Known Neches River Rose-Mallow Occurrences
----------------------------------------------------------------------------------------------------------------
First and last Plant estimates (or
Site County observation otherwise noted)
----------------------------------------------------------------------------------------------------------------
1. Compartment 55, Davy Crockett Houston.................... 2002-2003; 2011 750 in 2002; 500 in 2005;
National Forest (NF). 1,000 in 2006; in 2007 and
2008, no changes from
2006; 750 in 2010; 100-200
plants in October 2011;
407 stems in October 2011.
2. Compartment 16, Davy Crockett NF Houston.................... 2000; 2011 450 in 2000; 115 in 2002;
(introduced). 78 stems in 2003; 40 in
2004; between 20 and 40 in
2005; 50 in 2006; in 2007
and 2008, no changes from
2006; 90 in 2010; 43 stem
clusters in 2011.
3. Compartment 11, Davy Crockett NF Houston.................... 2004; 2011 200 in 2004; 75 plants in
(introduced). 2005; 10 in 2006; in 2007
and 2008, no changes from
2006; 7 in 2010; 10 stem
clusters in 2011.
4. Compartment 20, Davy Crockett NF Houston.................... 2000; 2011 200-250 in 2000 (also
(introduced). reported that 350 plants
introduced); several
hundred blossoms in 2001;
70 in summer and fall of
2002; 182 in 2002; 291
stems in 2003; 100 in
2005; 350 in 2006; in 2007
and 2008, no changes from
2006, but only 150 seed
pods in 2007; 120 in 2010;
101 stem clusters in 2011.
5. SH 94 ROW-Boggy Slough.......... Trinity.................... 1955; 2011 100+ in 1968; 50 in 1986;
50 in 1987; 13 in 1988; 7-
9 in 1991; 2-3 in 1992;
maximum of 27 in 1993; 38
in 1994; 41 in 1995; 16 in
1996 (only a partial
survey); 15-20 on private
land in 1997; 13 in 1998;
49 in 1999; 17 along ROW
and 300 observed on
private land in 2000; 15
and 300+ on private land
in 2001; 20 along ROW and
fewer than 100 observed on
private land in 2002; 3 in
2003; 20 and 0 on private
land in 2005; none in
2007; 35 along powerline
in 2010; 128 stem clusters
along ROW in 2011.
6. SH 204 ROW-Mud Creek............ Cherokee................... 1992; 2011 1 in 1992 and 1993; 26
within 3 subpopulations in
fall 1993; 1 in 1994-1996;
1 observed then an
additional 75 in 1997
under bridge; 1 in 1998; 2
in 1999; 16 in 2000; 5 in
2001; none in 2002; 17 in
2003; none in 2004, 2005,
2008, 2009; 46 in 2010 in
4 subpopulations; 1 plant
in one subpopulation in
summer 2011; 20 stem
clusters in 6
subpopulations in 2011.
7. SH 230 ROW...................... Houston.................... 1978; 2002 50 in 1991; 58 in 1993; 38
in 1994; 1 in 1995; 2 in
1996; 6 in 1997; 8-13 in
1998; 14 in 1999; 8 in
2000; 4 in 2001;12 in
Sept. 2002; none in Oct.
2002, 2003, 2004, 2005, or
2011. Considered
extripated.
8. Lovelady........................ Houston.................... 2011 50-70 in 1991; 7 in 1992;
58 in 1993; several
hundred blossoms in 2001;
400 along ROW in 2002; 900
blossoms or seedpods in
2007; observed in 2008,
but no estimates; 20 in
2010; 539 stem clusters in
2011.
9. Mill Creek Gardens (introduced). Nacogdoches................ 1995; 2011 96 in 1995; hundreds in
October 2011.
10. Harrison Site.................. Harrison................... Not observed Herbarium specimen was
after 1980 recently confirmed again
as H. dasycalyx, but site
has not been observed
since 1980.
11. Champion site.................. Trinity.................... 1996; 2001 Hundreds in 1997; 300-400
in 2001.
12. Camp Olympia................... Trinity.................... 1977; 1978 No estimates. Searches
occurred in 1992 and 1993,
but no plants were
observed.
----------------------------------------------------------------------------------------------------------------
Populations along SH ROWs include SH 94 in Trinity County,
collected in 1955 (Blake 1958, p. 277); SH 204 in Cherokee County,
first observed in 1992; and SH 230 in Houston County, first observed in
1978. The TPWD performed annual SH ROW monitoring along SH 94 from 1993
thru 2001 (Poole, 2001, p. 1); along SH 204 from 1993 thru 2003 (Poole
2001, p. 1; TXNDD 2012a, pp. 20-28); and along SH 230 from 1993 thru
2001 (Poole 2001, p. 1). These three ROW populations are separated from
one another and are considered distinct. However, the Boggy Slough site
consists of several scattered Neches River rose-mallow subpopulations
that are located in close proximity to one another. Boggy Slough
subpopulations and the SH 94 ROW population are separated by no more
than 1.0 km (3,280 ft), and these two sites likely constitute a single,
larger population, sharing pollinators and exchanging genetic material
(NatureServe 2004, p. 6; Poole 2011c, p. 2). Therefore, in Table 4,
they are combined and represented as a single location.
Adjacent lands to the SH 230 ROW were purchased by the Texas Land
Conservancy in 2004 (The Texas Land Conservancy 2011), an organization
previously known as the Natural Areas Preservation Association (NAPA).
The Neches River rose-mallow plants in this site, referred to as
Lovelady, are part of a population that included the Neches River rose-
mallow plants in the SH 230 ROW. The Neches River rose-mallow plants
within the SH 230 ROW have not been observed since 2002, and the site
is considered extirpated (TXNDD 2012a, pp. 61-67). The Lovelady site
was recently surveyed in 2011, and although 539 stem clusters were
found, most were in notably poor condition, being much shorter in
stature because of the drought and herbivory (Poole 2012b, pers. comm.;
TXNDD 2012a, pp. 14-19). The estimates of Neches River rose-mallow
displayed in Table 4 show wide variations in plant numbers. Some of
this variation is due to incomplete counts at the sites; in other
words, only a portion of the population was counted. Meaningful trends
cannot be derived from these population estimates.
Although annual monitoring of the ROW sites was discontinued in the
early 2000s, TPWD visited all of the ROW sites in October 2011. In the
past, along SH 204 ROW, several subpopulations existed along multiple
portions of the ROW; however, several of these subpopulations were gone
in 2011. The recent drought conditions have allowed surveyors to count
Neches River rose-mallow plants in parts of sites that were not
accessible in the past because the sites were too wet. The increase in
[[Page 56034]]
numbers of plants at some of the ROW sites may be partially attributed
to this.
The Davy Crockett NF, Houston County, Texas, contains four extant
sites, three introduced and one natural, of the Neches River rose-
mallow. The one natural population is found in compartment 55 located
west of the Neches River. This site is considered the most robust of
all known extant populations (Poole 2011c, p. 3) and is almost entirely
unaltered from its originally observed state as a seasonally wet
flatwood pond, with vegetation being distinctly zoned (TXNDD 2012a, p.
29). The three introduced populations are located in compartment 16,
which was introduced with 450 plants (Davis 2000, pers. comm.;
McCormick 2002, p. 1; Service 2000, p. 3); compartment 20 with 200-250
plants (Davis 2000, pers. comm.; McCormick 2002, p. 2; Service 2000, p.
3); and compartment 11 with about 200 plants (Nemec 2005, pers. comm.).
The populations in compartments 16 and 20 were introduced in 2000,
while the population in compartment 11 was introduced in 2004 (Service
2007, p. 6). All four of the Davy Crockett NF sites were censused in
October 2011, by the Service and TPWD, and all of the introduced sites
on the Davy Crockett NF appear to have declined dramatically.
The four remaining Neches River rose-mallow sites have had sporadic
monitoring or have not been visited in recent years. In 1995, Stephen
F. Austin State University Mast Arboretum planted 96 Neches River rose-
mallow plants into a site at Mill Creek Gardens, Nacogdoches County
(Scott 1997, pp. 6-7). A conservation easement was placed on this land,
and now the site is managed by the Mast Arboretum. Neches River rose-
mallow plants at this site were observed in 1997, 1998, 2001, 2009, and
2011 (Creech 2011a, pers. comm.). The introduced plants appear to be
doing well; however, nonnatives and native species are becoming more
prevalent, and may compete with the Neches River rose-mallow (Creech
2011c, pers. comm.). Another site in Harrison County, Texas, was last
verified by a specimen collected in 1980. The identification of this
specimen was identified as Neches River rose-mallow and later
considered Hibiscus laevis (Melinchuk 2012, p. 2). Not until 2011, was
it confirmed that the specimen collected was the Neches River rose-
mallow (Birnbaum 2011, pers. comm.; TXNDD 2012a, pp. 12-13). Although,
the Harrison County site has not been visited since 1980, and drought
and severe storms might have impacted this site but without a lack of
evidence suggesting the species' extirpation from either threat, we
presume that Neches River rose-mallow is extant at this site. Two
additional populations occur on private lands in Trinity County: the
Camp Olympia and Champion sites, discovered in 1977 and 1996,
respectively. The current status of Neches River rose-mallow on the
Camp Olympia site is unknown. We consider this site to be extant
because we have no evidence that it has been extirpated. The population
on the Champion site was observed in 2001; plants were seen, but no
plant counts were done.
Conservation
We relied on Pavlik's Minimum Viable Population analysis tool
(1996, pp. 127-155) and species' experts to determine the conservation
goals of the species. Based on the best known and available scientific
information on the species' life-history and reproductive
characteristics, we concluded that the conservation goals for the
Neches River rose-mallow include 10 viable populations, each containing
at least 1,400 individual plants. The species is limited to the Neches,
Sabine, and Angelina River basins and the Mud and Tantabogue Creek
basins with 11 extant sites throughout this range. However, many of
these sites were introduced and are now compromised by threats from
feral hog damage, hydrological changes, nonnative and native species
encroachment into habitat, construction projects, and herbicide
overspray. Future management actions that ameliorate these threats
could allow for the species to expand within its known range. The
extant populations are generally small. The only site that has come
close to reaching the conservation goals is on compartment 55 of the
U.S. Forest Service (USFS); however, it still only comprises 53 percent
of the needed plants at this site (750 plants were seen in 2010).
Summary of Comments and Recommendations
We requested written comments from the public on the proposed
listing for the Texas golden gladecress and Neches River rose-mallow
during two comment periods. The first comment period, associated with
the publication of the proposed rule (77 FR 55968), opened on September
11, 2012, and closed on November 13, 2012. Newspaper notices inviting
general public comment were published in the Houston County Courier,
Nacogdoches Daily Sentinel, and Marshall News Messenger. We also
requested comments on the proposed listing during a comment period that
opened April 16, 2013, and closed on May 16, 2013 (78 FR 22506). We
received requests for a public hearing, which was held on May 1, 2013,
in Nacogdoches, Texas. Newspaper notices inviting public comment for
this second comment period were published in the San Augustine Tribune
and Cherokeean Herald in addition to the three papers listed above. We
also contacted appropriate Federal, State, and local agencies;
scientific experts and organizations; and other interested parties and
invited them to comment on the proposed rule during these comment
periods.
We received approximately 63 public comments. All substantive
information provided during both comment periods has either been
incorporated directly into this final determination or is addressed
below. Comments addressed below are grouped into general issues
specifically relating to the listing of Texas golden gladecress and
Neches River rose-mallow.
Peer Review
In accordance with our peer review policy published on July 1, 1994
(59 FR 34270), we solicited expert opinions from six knowledgeable
individuals with scientific expertise that included familiarity with
the biology and ecology of the Texas golden gladecress and Neches River
rose-mallow; the geographic region in which these species occur and
characteristics of their habitats, including the unique geology; and
land uses common to the region that may bear on the threats to both
species. We received responses from four of the peer reviewers.
We reviewed all comments we received from the peer reviewers for
substantive issues and new information regarding listing of the Texas
golden gladecress and Neches River rose-mallow. The peer reviewers
generally agreed with portions of our assessment, including the threats
analysis, and most of our conclusions, although they pointed out areas
where additional research would refine our understanding of the two
species' habitat requirements and range. The peer reviewers provided
additional information, clarifications, and suggestions for future
research that would inform future surveys to refine the geographic
range and that would help with management and recovery efforts. Peer
reviewer comments are addressed in the following summary and
incorporated into the final rule as appropriate.
Peer Reviewer Comments
(1) Comment: One peer reviewer asked for clarification regarding
the
[[Page 56035]]
numbers of Texas golden gladecress populations in State highway ROWs.
One location in the proposed rule referred three extant sites within
State highway ROW; however, another location refers to only two extant
populations within State ROWs.
Our Response: We recognize that the language in the proposed rule
may be misleading or easily misconstrued because it implies that the
three confirmed Texas golden gladecress populations are all located in
ROWs. We have changed the language in the referenced paragraph to
reflect the fact that only two of the extant populations, Geneva and
Caney Creek Glade Site 1, occur in ROWs, which are both managed by
TXDOT. The third extant population at Chapel Hill is located on a small
tract adjacent to a county road and is not considered to extend into
any type of road ROW.
(2) Comment: One peer reviewer stated his opinion that that there
is no conservation land, fee simple or under easement, for either of
these species. He alluded to the land on which these species' habitats
occur being some of the cheapest in east Texas and suggested that it
would be more cost effective to purchase fee title or conservation
easements of small tracts to conserve these species because creation of
a series of small protected sites would work well for an endemic
species. He indicated that the habitat areas in question have very
little commercial value, with the Weches glades having no value for
forestry or agriculture. He acknowledged that the value of the Weches
Formation for glauconite mining exceeds values for other uses and
indicated his opinion that it would be appropriate to estimate the
commercial value of the glauconite mined on a site and match this
value.
Our Response: We are in agreement with the first part of this
comment about the lack of conservation lands for the Texas golden
gladecress; however, this is not true for the Neches River rose-mallow.
The Texas Land Conservancy has fee title ownership of the land on which
the Neches River rose-mallow's Lovelady population in Houston County is
located. The Texas Land Conservancy bought this land specifically to
conserve the Neches River rose-mallow and manages the site accordingly.
The United States Forest Service (USFS) also has Neches River rose-
mallow in several compartments, is aware of the species, and manages
those compartments to avoid impacts.
Further, the Act requires us to determine if the Texas golden
gladecress and Neches River rose-mallow warrant listing solely on the
basis of the best scientific and commercial data available as evaluated
through our assessment of the five listing factors set forth in the
Act. We previously determined that the Texas golden gladecress and
Neches River rose-mallow warranted listing under the Act, making them
candidate species. However, the listing of these species was precluded
by the necessity to commit limited funds and staff to complete higher
priority listing actions for other species. The Texas golden gladecress
and Neches River rose-mallow have been included in our annual candidate
notices of review for multiple years. In our annual review of these
species, scientific literature and data have, and continue to, indicate
that these species are impacted by ongoing threats. Any future
conservation actions, such as purchasing land from willing landowners,
or land management efforts to ameliorate threats, will be evaluated as
part of the recovery planning process.
(3) Comment: Two peer reviewers discussed the geography of the
Weches Formation and wondered how it may influence the range of the
Texas golden gladecress. One reviewer indicated that it is a common
misconception that the Weches Formation centers on Nacogdoches and San
Augustine Counties. He pointed out that the Weches Formation also
extends over 100 miles (161 km) to the north into Smith, Wood, Upshur,
Marion, and Cass Counties in Texas, and even across into Miller County,
Arkansas. A second reviewer described the Weches formation as
consisting of Eocene age deposits lying mostly in an east-west band.
This reviewer further pointed out a northeast to southwest trend in
Cherokee County, Texas, proceeding northeastward toward Tyler, Texas.
Referencing the U.S. Department of Agriculture's soils surveys of
Cherokee, Nacogdoches, Houston, San Augustine, and Sabine Counties, the
reviewer indicated that most acreage of Weches Outcrop may occur in
Cherokee County. The former reviewer indicated that he was not aware of
any systematic surveys of these widely dispersed outcrops for the
presence of the endemic glade plants. He recommended that some
attention and resources be directed at exploring the other Weches
outcrops that stretch north to Cass County and suggested that any
ruling by the Service or subsequent recovery plan for Texas golden
gladecress include provisions for surveying these areas.
Our Response: The Service recognizes the extent of the Weches
Formation reaches the above referenced counties. However, the Service
has not found or received any data indicating that the species is
present in these other counties. The Service is required to use the
best scientific and commercial data available at the time of listing.
We relied on all available information regarding the known occurrences
of the Texas golden gladecress at the time of listing; none of the
known occurrences was reported from outside Sabine and San Augustine
Counties (with the exception of the introduced population in
Nacogdoches County). Further analysis of geological correlations with
the Texas golden gladecress is an issue to be addressed in recovery
planning. Furthermore, as a federally listed endangered species, the
Texas golden gladecress will be afforded the protections of the Act
wherever found.
(4) Comment: One peer reviewer pointed out that our assessment of
the Weches Formation did not take into account the work of geologists.
He suggested referencing the body of work on the chemistry and
mineralogy of the Weches by Ernest Ledger and students that document a
wide variation in the attributes of the Weches across its range from
San Augustine and Nacogdoches Counties, north over 100 miles (161 km)
to Cass County. In his opinion, we need to know about the variability
of the Weches Formation in terms of available calcium and long-term pH
change to identify more potential sites for the Texas golden
gladecress. This reviewer indicated that Ledger's chemical analyses of
Weches constituent minerals shows hard data on the low-level presence
of nutrients in some locations. Some of these may be suitable for
mining as soil additives in the future when current sources like
phosphate rock deposits are mined-out. Analyses of the chemical
composition of the rock should be considered when selecting potential
conservation sites. He suggested that a critical look at Ledger's work
might show that unusual features of the Weches Formation that promote
the occurrence of Texas golden gladecress and associated glade plants
are limited to the southern end of the Weches Formation. Similarly,
this peer reviewer referred to the known variations in the Weches
Formation and suggests that we need a better understanding of the
geology and soils conditions underlying Texas golden gladecress in
order to plan for future surveys for the species.
Our Response: We recognize that variability of Weches outcrops does
exist across the Weches Formation throughout the numerous counties
listed above. We agree that a better characterization of the geology
and soils underlying known Texas golden gladecress populations could
provide useful information. However, there are
[[Page 56036]]
likely other factors that characterize individual outcrop sites that
may also be important (for additional information, see ``Invasive
Species'' under A. The Present or Threatened Destruction, Modification,
or Curtailment of Its Habitat or Range of this rule). Further, the
Service must use the best available scientific and commercial data
available at the time of listing. Determining the chemical components
of the geological formations beneath known glade sites is not a
feasible accomplishment within the timeframe we have to publish our
final determination. This research would be addressed in recovery
planning. For purposes of the proposed rule and this final rule to list
the Texas golden gladecress, we used the more general Weches Formation
outcrops descriptions, and we more specifically relied on the geologic
and soils information available from one known Texas golden gladecress
population site, as well as from one white bladderpod site. Please see
the ``Habitat'' section for the Texas golden gladecress in this final
rule for more information.
The commenter did not provide specific references for Ledger's
research. However, we attempted to locate research conducted by Ledger
on this topic. We were able to locate some of Ledger's research, and we
incorporated this into this final rule under the ``Habitat'' section
for the Texas golden gladecress. However, this information did not
modify our conclusions of our analysis of threats or determination that
the species meets the definition of an endangered species under the
Act.
(5) Comment: One peer reviewer commented that the essential habitat
component of Weches outcrops underlying Texas golden gladecress
populations is the combination of thin soil over a calcium-rich parent
material. In the Weches Formation, the calcium is derived from a myriad
of fossilized, calcium-dominated oyster shells and other marine life.
Our Response: The peer reviewer's verbiage was added to the Texas
golden gladecress's ``Habitat'' description in this final rule to
further illustrate the derivation of calcium from marine organisms that
is true of the east Texas Weches Formation and which may be different
from habitat of other Leavenworthia species.
(6) Comment: One peer reviewer indicated that the developed soils
that occur near the Weches outcrops are included in the Bub, Trawick,
Nacogdoches, or Chireno soil series. He described the Chireno soil
series as unique because it is the only ``blackland soil'' in east
Texas. Chireno soils are classified as ``mollisols'' or blackland soils
and are developed under prolonged grassland habitat. This reviewer used
the U.S. Department of Agriculture's soil surveys for Sabine, San
Augustine, Nacogdoches, and Houston Counties to estimate roughly 3,000
acres (1,214 ha) of this soil type occurring in a four-county area. He
indicated that these soils may underlie prairies (glades) and that
Native Americans regularly burned these areas either for protection
from wildfires or enemies, or to entice game animals.
Our Response: Although the reviewer does not specifically suggest
that we add Chireno soils to the other soils known to support Texas
golden gladecress habitat, this is how we have interpreted his comment.
Based on the development of these blackland soils being dependent on
long-term prairie cover, and the fact that other literature describes
the Pineywoods glades as being within prairies, or as part of a
combination of prairies and glades, information may indicate the
potential for Weches outcrops within this soil series to support the
herbaceous glades of which Texas golden gladecress may be a component.
Mollisols, of which the Chireno series is one, are soils of grassland
ecosystems, characterized by a thick, dark surface horizon that was
developed under prolonged grassland habitat (Grunwald 2013, pp. 1-2).
We based the soil parameters for Texas golden gladecress habitat on the
soil descriptions in the TXNDD's element of occurrence records, the
thesis by Robert George (George 1987, entire), and the U.S. Department
of Agriculture's soil survey layers underlying all known Texas golden
gladecress populations. The known Texas golden gladecress occurrences
are all found on shallow, gravelly soils or almost bare bedrock
overlying Trawick, Bub, or Nacogdoches soils, situations that would not
support dense stands of prairie grasses, at least in the portion of the
outcrop where the Texas golden gladecress is growing. Further
investigation of the Chireno series for the presence of Texas golden
gladecress would be addressed during the recovery process.
(7) Comment: One peer reviewer provided us with confirmation that
the glade habitat at the Texas golden gladecress population site
referred to as Caney Creek Glade 7 was still intact as of spring 1996,
when this reviewer visited the site. However, on a second visit in
2000, encroachment by weedy and woody species was prevalent at this
site.
Our Response: This comment affirms our 2012 evaluation of this
site, as derived from analysis of satellite imagery. As indicated in
our proposed rule and this final rule, the population being referenced
may still be present as of 2012, but from satellite imagery the site
appeared to be overgrown with woody vegetation. Based on the habitat at
Caney Creek Glade Site 7 remaining intact (not excavated or built
over), with the exception of woody overgrowth, we assume that Texas
golden gladecress plants still occupy this site.
(8) Comment: One peer reviewer relayed personal observations that
accumulation of pine leaf litter and eventual degradation of the
material supports the germination of pine seed. This reviewer indicated
that this likely happens because the leaf litter debris provides a
small but steady increase of soil depth on the rocky, thin soil common
in the Weches glades.
Our Response: This comment supports the data in our proposed rule
and this final rule to list the Texas golden gladecress, which state
that planting of pine trees in close proximity to small glades may
produce leaf litter that can accumulate within a glade, sometimes
covering its surface and smothering smaller glade plants. As noted by
the reviewer, the accumulation of pine leaf litter and the byproducts
of its decomposition would create and enhance layers of organic
material and create conditions favorable to natural pine seedling
establishment. This would alter the nature of the glades by eventually
deepening soils within the glade, thereby allowing other plants,
including woody plants that previously did not occur in the short,
herbaceous plant community, to take over these areas that formerly had
too shallow and poor soil to support shrubs and trees. This situation
would also enhance invasion by other plants, including Macartney rose,
that would benefit from additional soil. Not only would the glade
vegetation undergo succession to shrubs and trees, but the glades would
also be altered by the shading and would hold moisture in the soil. All
of these conditions would impede the continued existence of the Texas
golden gladecress by altering the competitive advantage that this plant
has in the glade environment.
(9) Comment: One peer reviewer suggested evaluating a specific,
potential Texas golden gladecress site based on the presence of the
Texas golden gladecress's known associated species. The site is located
on the SH 21 ROW, near the Sabine, Davy Crockett NF compartment 76,
adjacent to a glauconite quarry.
Our Response: From information provided to us early in the proposed
rule's preparation stage, we were aware
[[Page 56037]]
that flora and fauna surveys were done on USFS lands in Sabine County
in association with the debris cleanup effort post-Hurricanes Rita and
Ike. These surveys, in conjunction with results of botanical surveys
conducted before this time, failed to document the Texas golden
gladecress on any of these USFS lands, although we do not know if lands
outside of the USFS were included in any of the surveys. However,
strategies for continued evaluation of potential but unconfirmed new
sites will be addressed during the recovery planning process.
(10) Comment: One peer reviewer suggested that mention be made of
the possibility for illuminating the evolutionary history of these
species by genetic studies and that this would be useful in determining
management strategies.
Our Response: This is an issue that may be addressed during
recovery planning.
(11) Comment: A peer reviewer provided additional literature to
consider in our analysis on the hybridization of the Neches River rose-
mallow. One was by Klips (1995) and the other by Mendoza (2004). These
studies provide genetic insight of the relatedness between Neches River
rose-mallow and two co-occurring species, Hibiscus moscheutos and H.
laevis. Both researchers agree with the Service's opinion that the
Neches River rose-mallow is a distinct species. These studies review
the relatedness between the Neches River rose-mallow and other species;
however, they do not investigate hybridization. Another peer reviewer
noted the potential hybridization of the Neches River rose-mallow on
compartment 20 in the Davy Crockett NF, in October 2012. Plants
appeared to be H. dasycalyx, but the calyx was lacking the hairy
surface typical of the species. The reviewer thought that the species
was a potential cross with H. laevis.
Our Response: The Service has reviewed this new information and
incorporated it into the threats section under ``Hybridization'' in
this final rule. These studies pertain to the relatedness between the
Neches River rose-mallow and other species. They do not investigate
hybridization of these species. Although the genus Hibiscus readily
hybridizes within the nursery trade, hybridization between Neches River
rose-mallow and another Hibiscus under natural conditions has not been
verified. Drought conditions can alter the plants morphological or
physical characteristics including leaf size, structure, and overall
plant height (Fair 2009, p. 1). Further investigation into the
occurrence of hybridization and its impacts on the population are
necessary. The University of Texas-Tyler is researching the
hybridization issue for Neches River rose-mallow and its impacts on the
population; however, the project is only in its infancy, and no results
have been determined. We do not consider hybridization a threat to the
Neches River rose-mallow at this time.
(12) Comment: One peer reviewer reported that in October 2012, she
and a USFS botanist observed sedimentation along ROW work on both sides
of SH 94. They anticipated that resurfacing and re-crowning work of the
highway will likely increase runoff to this site. The reviewer noted
that, during road improvement, TXDOT installs temporary culverts to
assure water flow and exchange during construction. Another reviewer
questioned whether county and municipal governments, who buy glauconite
for road projects, are required to demonstrate that endangered species
like white bladderpod are not being negatively impacted by their road-
building activities. He further asked whether the counties are
receiving State or Federal funds to assist with road building.
Our Response: The Service is aware of the bridge replacement along
SH 94, but as of 2011, the construction and associated impacts of this
project had not progressed into Neches River rose-mallow habitats
(Adams 2011c, pers. comm.). Since the start of the SH 94 road expansion
project, TXDOT has employed the use of temporary culverts and orange
construction fencing around Neches River rose-mallow sites and has
restricted workers from these fenced-off areas. Fenced-off areas
encompassed far more area than that habitat known to be occupied by the
Neches River rose-mallow (Adams 2013b, pers. comm.). In wetlands where
sedimentation might continue despite the use of the above management
activities, silt curtains (or silt fence) placed in conjunction with
orange construction fencing have been installed (Adams 2013b, pers.
comm.). Currently, all avoidance measures are voluntary.
However, on the effective date of this final rule (see DATES), the
Neches River rose-mallow will become a federally threatened species
under the Act. Section 7(a)(2) of the Act requires Federal agencies to
ensure that activities they authorize, fund, or carry out (that is,
projects with a Federal nexus) are not likely to jeopardize the
continued existence of the species or destroy or adversely modify its
critical habitat, if any is designated. If a Federal action may affect
a listed species or its designated critical habitat, the responsible
Federal agency must enter into consultation with the Service (see
Available Conservation Measures in this final rule for more discussion
of this process). If this project, or any other project, has a Federal
nexus and the project may affect a federally listed species then the
Federal action agency will need to consult with the Service. We are
publishing a final rule on the designation of critical habitat the
Texas golden gladecress and the Neches River rose-mallow under the Act
elsewhere in today's Federal Register.
(13) Comment: One peer reviewer made several comments on invasive
species and provided the Service with new information on the biology of
Chinese tallow. The reviewer's recent observations in 2012, along with
a USFS botanist, found Chinese tallow and Melia azedarach (Chinaberry)
within compartment 16, Davy Crockett NF. Chinese tallow has invaded all
known Neches River rose-mallow sites, yet is more prominent in SH 94
and compartment 16, Davy Crockett NF sites. The reviewer provided a
literature citation, Gan et al. 2009. Additionally, the reviewer
mentioned that coastal bermudagrass (Cynodon dactylon) is one of the
most serious, nonnative, invasive species threats to the Neches River
rose-mallow.
Our Response: As described in the proposed rule, we agree with the
peer reviewer that nonnative species are a threat to the Neches River
rose-mallow. We incorporated the additional information and biological
data on tallow provided in Gan et al. 2009 into the Summary of Factors
Affecting the Species section of this final rule. This additional
information did not modify our listing determination.
At the time the proposed rule was published, we were only aware of
one location at Boggy Slough in Houston County where coastal
bermudagrass was observed. However, new information was provided to the
Service during a public comment period. We are now aware of three
additional sites where encroachment from coastal bermudagrass was
observed. These sites included: The Texas Land Conservancy, where it is
common; SH 204 ROW, where it is abundant (Poole 2013a, pers. comm.);
and the original site at the SH 94--Boggy Slough, where it is locally
common in the interior of the unit (Allen 2011a, pers. comm.). At the
planted site on Boggy Slough, Neches River rose-mallow was observed as
recently as August 2012. Although the coastal bermudagrass has the
potential to spread and grow quickly, and has been known to form
monocultures along
[[Page 56038]]
highway ROWs, the Neches River rose-mallow and coastal bermudagrass do
not necessarily grow naturally in the same habitat. Coastal
bermudagrass is not typically found within wetland areas. Further, the
Neches River rose-mallow is a taller growing species, a feature that
prevents itself from being shaded out by coastal bermudagrass. Based on
the above information, the Service does not consider coastal
bermudagrass a threat at this time. The TPWD concurs with the Service
that coastal bermudagrass is not considered a threat at this time
(Poole 2013a, pers. comm.).
The nonnative species Chinaberry has not been previously noted at
any of the sites, including the site mentioned by the commenter,
compartment 16 on the Davy Crockett NF. The Service investigated this
comment further, and Chinaberry was not mentioned in the TXNDD database
information. Based on this information the Service does not consider
Chinaberry a threat at this time.
(14) Comment: A peer reviewer indicated that due to drought in
2011, the numbers of plants were a lot fewer than years previous in SH
94 ROW and compartment 55, Davy Crockett NF. On October 3, 2012,
observers went to specific locations in these compartments where plants
were known to occur, and none could be found. In 2013, rainfall has
been about average to date, but the reviewer concluded that effects
were evident from previous drought.
Our Response: We agree that drought has caused impacts to said
populations and likely other populations. Drought conditions have
reduced the number of plants and have stunted overall Neches River
rose-mallow plant growth (TXNDD 2012a, p. 8). We do not have knowledge
of how drought affects the Neches River rose-mallow on a larger scale
or how it impacts flowering or seed production. However, it is possible
that during drought conditions, floral characteristics that are
normally easily recognizable could be reduced and make identification
of Neches River rose-mallow more difficult (Poole 2012b, pers. comm.).
Since the Neches River rose-mallow is a wetland species, we understand
that drought conditions could continue to threaten the habitat as well
as the reproductive capability since it is likely that seed dispersal
is water-mediated. With the likelihood that seasonal or successive
year-round drought conditions will likely continue, ancillary threats
from trampling and herbivory may be exacerbated. Drought is discussed
in the Summary of Factors Affecting the Species in this final rule.
(15) Comment: One peer reviewer noted that in spite of the fact
that Sabine and San Augustine Counties have not seen major increases in
human population, there has been improvement of services, such as
communication lines, water lines, domestic gas lines, and power lines.
These actions occur primarily in ROWs, and some occur in areas that are
situated in potential Texas golden gladecress habitat.
Our Response: We acknowledge that the installation of new service
lines (e.g., communication, water, domestic gas, and power lines) could
potentially occur in more rural areas, and these activities typically
occur in road ROWs, such as where the Texas golden gladecress occurs.
There are two known Texas golden gladecress sites that extend into road
ROWs. When this rule is effective (see DATES), section 7 consultation
requirements and section 9 prohibitions under the Act will apply to the
Texas golden gladecress and Neches River rose-mallow. See our response
to Comment 12 and Available Conservation Measures for more discussion
of this process.
(16) Comment: One peer reviewer pointed out an example of the flaws
of teaming these two species together can be seen in the statement in
the proposed rule that says, ``Prolonged or frequent droughts can
exacerbate habitat degradation for both species.'' He indicated that a
river-bottom dwelling species like the Neches River rose-mallow might
be negatively impacted when drought allows other species to encroach.
However, drought could positively impact Texas golden gladecress as it
might exclude woody closure of glades. This reviewer noted his personal
observation of the drought of 2011 dramatically pushing back the edges
of glades in the Weches and in tiny saline prairies.
Our Response: We agree that the droughty conditions of hot, dry
summers are a part of the reason why Texas golden gladecress can remain
competitive on the glades. However, prolonged drought, especially when
it occurs in successive years, has resulted in Texas golden gladecress
not appearing above ground in some years, and therefore not flowering
or producing seed in those years. We do not know how many years of poor
seed production, or no seed production at all, will affect the survival
of the population. Negative impacts of drought on the Neches River
rose-mallow are discussed in our response to Comment 14 as well in the
Summary of Factors Affecting the Species section of this final rule.
(17) Comment: A peer reviewer commented on the occurrence and use
of nonnative and potentially invasive pasture grasses such as coastal
bermudagrass, Paspalum notatum (bahiagrass), and Lolium perenne
(perennial ryegrass), which are commonly used to re-vegetate many road
ROWs. These grasses are common on most ROWs and aggressively grow in
open, sunlit areas.
Our Response: The Service recognizes the occurrence and use of
nonnative and potentially invasive pasture grasses along ROWs, and that
ROWs typically become monoculture stands of these invasive species,
thereby out-competing natives. The Service has verified that both
coastal bermudagrass and bahiagrass are included in mixtures used to
re-seed ROWs (Adams 2013c, pers. comm.). There are two Texas golden
gladecress and three Neches River rose-mallow known populations growing
along ROWs, which could be planted with nonnatives. We are not aware of
any Texas golden gladecress sites where the Texas golden gladecress
itself is being impacted by these grasses. Coastal bermudagrass has
been observed on four Neches River rose-mallow sites (see our response
to Comment 13 for additional details). We investigated these nonnative
species as potential threats and incorporated this information into our
analysis in the Summary of Factors Affecting the Species section for
the Texas golden gladecress and Neches River rose-mallow in this final
rule. There is the potential for such nonnative, invasive species to
impact the Neches River rose-mallow, as well as the Texas golden
gladecress, in the future if these grasses out-compete native plants
for soil nutrients, space, and light. However, these invasive species
are not currently a threat, and there are no data indicating that these
species will be a threat in the near future.
(18) Comment: One peer reviewer provided new observations about
damage to habitat due to feral hog activity. In October 2012, feral
hogs had broken and flattened plants in compartment 16, Davy Crockett
NF. Large groups of feral hogs were seen in two Neches River rose-
mallow sites (compartment 55 and compartment 16, both in the Davy
Crockett NF). Neches River rose-mallow habitat is only surficially dry
and can be easily disturbed by hogs, as made evident in compartment 20,
Davy Crockett NF.
Our Response: The Service has included this information in our
analysis of feral hog impacts on the Neches River rose-mallow in the
Summary of Factors Affecting the
[[Page 56039]]
Species section in this final rule. Based on this information, the
Service recognizes that feral hogs impact the species and that feral
hogs will likely continue to impact the species in the near future.
However, at this time, the severity of impacts to the species is low.
The level of impacts from feral hogs does not change the determination
to list the species as threatened versus endangered.
(19) Comment: One peer reviewer commented on the impacts that
beavers have had on one Neches River rose-mallow site: Compartment 16,
Davy Crockett NF. In general, water levels fluctuated due to beaver
activity. It was observed that larger trees along the water's edge were
damaged by beavers, although it appears that water levels had receded
to the same level prior to the beaver activity.
Our Response: The Service is aware of beaver presence at
compartment 16 of the Davy Crockett NF. We acknowledge that beaver
activity (i.e., dams) could have impacted this Neches River rose-mallow
site. However, with seasonally fluctuating water levels and no
estimates on plant abundance before and after beaver activity, it is
unclear how or if beaver activity was a factor in the size of the
Neches River rose-mallow population. We are uncertain if there was a
correlation between the damage done to this site and the changes in
water flow and the site hydrology, and whether this had a positive or
negative impact on the species. No other sites have been impacted by
beaver activity. We do not consider the effects of beaver damming to be
a threat to the Neches River rose-mallow.
(20) Comment: One peer reviewer agreed with the use of Weches
glauconite as road base material being a threat. He indicated his
belief that it should be possible to locate Weches mines where
conditions are not suitable for the glade community and reiterated that
the Weches is a highly variable rock formation. This peer reviewer
provided new information about other uses for Weches glauconite,
including animal feed additives, that were not addressed in the
proposed rule. This reviewer expressed his opinion that it is also
possible that in a few decades the shortage of mineral phosphate rock
might make some of the deposits viable for agriculture use. He referred
to information from Dr. Ernest Ledger (geologist) regarding instances
where rare earth elements are being mined in the Weches or Reklaw
Formations.
Our Response: In analyzing threats to a species, the Service uses
the best scientific and commercial data available to analyze the
current threats and threats anticipated to occur in the near future.
The Service has identified quarrying Weches glauconite as a current and
future threat to the Texas golden gladecress. We know that several
Texas golden gladecress populations have been lost in areas where
glauconite quarries were developed (see the Summary of Factors
Affecting the Species sections of the proposed rule and this final
rule). We did not specifically identify animal feed additive as a use
for the Weches glauconite in our proposed rule, but we have
incorporated this information into the Summary of Factors Affecting the
Species section of this final rule. The impact to the species from
quarrying is the clearing and excavation of vegetation and soil during
development. The specific uses of the Weches glauconite are not
relevant to the impacts from quarrying. However, new uses or an
increase in current uses of Weches glauconite may increase the demand
of this resource and therefore increase the amount of quarrying
activities (that is, ground disturbance). However, the Service does not
have information that either of these are occurring.
Section 7 of the Act requires Federal action agencies to consult
with the Service to ensure their action do not jeopardize the continued
existence of the species. However, there are limited or no Federal
nexuses for glauconite quarry projects. Entities implementing projects
that could impact the Texas golden gladecress could play a significant
role in the conservation of the species by voluntarily working with the
Service, the State, or conservation groups to construct their projects
in such a way as to avoid or minimize impacts to the species. Site
selection of quarries outside of endemic plant communities containing
Texas golden gladecress could be a measure to avoid or minimize impacts
to the species.
Additional research of the habitat requirements of the Texas golden
gladecress, particularly the surface soils and subsurface composition
of the bedrock, may help in determining whether there are particular
outcrops that should be protected for Texas golden gladecress versus
ones that will never support the species and would therefore not be
problematic if selected for a quarry. This is an issue that may be
addressed during recovery planning.
(21) Comment: One peer reviewer suggested using genetic evidence to
evaluate how past climate changes, particularly drought, as well as
dispersal mechanisms and barriers to dispersal, may have affected the
distribution and endemism of the Texas golden gladecress and the Neches
River rose-mallow. He indicated his opinion that a better understanding
of these factors would have bearing on future management
considerations.
Our Response: It is possible that the past droughts have affected
the distribution of Neches River rose-mallow and Texas golden
gladecress in east Texas. For Neches River rose-mallow, geographic
barriers may have arisen due to past drought events, potentially
limiting genetic exchange between populations. Humans may have
contributed to further endemism of the species by altering habitat,
which functionally created barriers to dispersal and resulted in more
isolation of populations. However, we can only postulate that these are
the reasons for the endemism of the Neches River rose-mallow to certain
river systems, and more specifically to surficially dry habitats as
compared to other east Texas Hibiscus species. Additional research is
needed to assess the validity of this hypothesis.
With regard to the Texas golden gladecress, the Weches outcrops
generally occur in small, isolated or segmented strips (George 1987, p.
4; George and Nixon 1990, p. 118), making the habitat, in essence,
small islands separated from one another by dissimilar habitat. The
current patchiness and separation of the Texas golden gladecress
population sites may be, at least in part, due to past droughts, but
may also be a result of the habitat being fragmented by land
conversions or lost to succession by woody species. Because we lack
information on seed dispersal of Texas golden gladecress, we do not
know how the species spread historically or how it came to be
distributed where it is. Therefore, we do not know if the isolation of
the populations is due to vicariance (populations on outcrops that are
geographically separated by surrounding forest) or due to a lack of
dispersal to new habitats or between population sites. Genetic evidence
may help to clarify the relatedness or lack thereof between the
remaining extant populations, but that may be undertaken as part of the
recovery process.
(22) Comment: One peer reviewer commented that the presence of a
currently listed endangered species, white bladderpod, confers some
protection for other Weches glade plants at sites where it occurs.
Our Response: There are two Texas golden gladecress sites where
white bladderpod is also found: Chapel Hill and Caney Creek Glade Site
1. Additionally, both species were known to co-occur at historical
Caney Creek
[[Page 56040]]
Glade Site 6, but they were eliminated by construction of a quarry. The
entirety of the Chapel Hill site is privately owned, with all Texas
golden gladecress plants growing strictly on private land. This
situation is also true for most of the Texas golden gladecress plants
at the Caney Creek Glade Site 1, although a limited number of
individuals extend into the adjacent TXDOT-managed ROW. Although there
are not formal legal protections for listed plants on private land, if
a project takes place on that privately owned property that is carried
out, permitted, or funded by a Federal agency, a Federal nexus is
established for that project, and that Federal action agency is
responsible for section 7 consultation with the Service to avoid
jeopardizing the species or adversely modifying any designated critical
habitat. For the plants in the ROW at Caney Creek Glade Site 1, TXDOT
will provide protections for the species per State regulations or
through consultation with the Service.
Comments From States
Section 4(i) of the Act states, ``the Secretary shall submit to the
State agency a written justification for his failure to adopt
regulations consistent with the agency's comments or petition.''
Comments received from the State agencies and government officials
regarding the proposal to list the Texas golden gladecress and Neches
River rose-mallow are addressed below.
(23) Comment: These species have not been fully studied. There are
significant concerns with the quality of data and analysis the Service
used for its determination. The proposal is based largely on
inconclusive reports and vast speculation about operations thought to
affect habitats, existing regulatory mechanisms, conservation efforts,
species populations and potential threats that fail to provide any
sound scientific foundation on which to justify the listing of these
species.
Our Response: It is often the case that biological information may
be lacking for rare species; however, the Act requires the Service to
make determinations based on the best scientific and commercial data
available after conducting a review of the status of the species and
after taking into account those efforts, if any, being made to protect
such species. We are also required to make our listing determinations
based on the five threat factors, singly or in combination, as set
forth in section 4(a)(1) of the Act.
We sought comments from independent peer reviewers to ensure that
our designation is based on scientifically sound data, assumptions, and
analysis. Peer reviewers were generally in agreement with the
conclusions from our threats analysis that habitat modification and
destruction due to human activities, as well as woody encroachment into
Weches glades, likely adversely affects the Texas golden gladecress.
The reviewers enhanced our understanding of some threats by providing
personal observations of habitat conditions at some population sites of
both species. A peer reviewer brought the ongoing installation of
utility service improvements with potential to impact Texas golden
gladecress in portions of its range to our attention. Peer reviewers
also agreed that drought negatively affects the Neches River rose-
mallow, and they provided new, detailed information on the types of
invasive plants that most seem to constitute a threat to the species,
as well as the extent of the invasion by these plants into Neches River
rose-mallow population sites. In addition, they furnished information
about the presence of feral hogs at specific Neches River rose-mallow
population locations, as well as observations of sedimentation from a
highway construction project into one Neches River rose-mallow site.
One peer reviewer indicated his agreement that the Neches River rose-
mallow lacks protective mechanisms other than U.S. Army Corps of
Engineers (USACE) permits. One peer reviewer expressed his opinion that
we needed more pertinent geological information on the outcrops across
a larger geographic area than just Nacogdoches, San Augustine, and
Sabine Counties. He also suggested chemical analysis of the outcrops
known to support the Texas golden gladecress so as to better understand
their unique qualities in order to use that information to seek out
additional sites to survey for heretofore undiscovered populations or
to carry out recovery actions.
We also solicited information from the general public,
nongovernmental conservation organizations, State and Federal agencies
that are familiar with the species and their habitats in east Texas,
academic institutions, and groups and individuals that might have
information that would contribute to an update of our knowledge of the
Texas golden gladecress and the Neches River rose-mallow, as well as
the activities and natural processes that might be contributing to the
decline of either species. We used information garnered from this
solicitation in addition to information in the files of the Service,
TPWD, TXNDD's elements of occurrence records for both species,
published journal articles, newspaper and magazine articles, status
reports contracted by the Service and TPWD, reports from site visits,
and telephone and electronic mail conversations with knowledgeable
individuals. We also used satellite and aerial imagery to ascertain
changes in land cover and land use at historical population sites and
to determine whether changes in land cover and land use at historical
populations sites and to determine whether the presence of primary
constituent elements for each species were still in place.
Additionally, we used the results of population monitoring from site
visits to look at abundance, and if enough information was available,
to get an idea of trends in the populations. In October 2011, we also
made field trips to known sites where we were granted access, to verify
land uses and contribute to the veracity of our threats analysis. In
March 2012, we helped to organize and carry out a workshop and field
tour of Texas golden gladecress sites for purposes of assisting
landowners and agricultural agencies to become familiar with the
species and its habitat. We also revisited accessible Texas golden
gladecress sites at that time. In August 2012, we attended a Neches
River rose-mallow workshop and field tour conducted by TPWD and
revisited Neches River rose-mallow population sites. We used the best
scientific and commercial information available in assessing population
status, recognizing the limitations of some of the information.
(24) Comment: There is no conclusive indication that glauconite
quarrying, oil and gas activities, invasive species, or pine tree
plantings threaten Texas golden gladecress.
Our Response: As stated in the proposed rule and this final rule,
three historical populations of Texas golden gladecress were documented
from sites where glauconite quarries are now located. The sole
introduced Texas golden gladecress population, in Nacogdoches County,
was extirpated by construction of a pipeline as recently as 2011. The
Weches glades are documented to be overgrown with invasive, native and
nonnative plants. The potential for negative effects from pine trees,
planted in such close proximity to glades that shading and leaf litter
accumulations adversely affect the glades, was pointed out to us by
several respondents during the comment periods on the proposed rule, as
well as one of our peer reviewers based on their personal observations
(see the Summary of Factors Affecting the Species section of this final
rule).
[[Page 56041]]
(25) Comment: There is no conclusive indication that the invasion
by other species, development and construction projects, herbicide use,
or herbivory pose a risk of loss or degradation to the Neches River
rose-mallow.
Our Response: A thorough analysis of the impacts of nonnative and
native species encroachment, TXDOT roadway construction and maintenance
projects, herbicide use, and herbivory were discussed in the proposed
rule and in this final rule. All populations of the Neches River rose-
mallow have been encroached upon by Chinese tallow. This invasive
species is fast-growing and, once established in a habitat, is highly
destructive, choking out native species. Development and construction
projects will likely continue to be a threat to the species. Herbicides
are a threat that could impact 7 of 11 (64 percent) Neches River rose-
mallow populations. We do not consider herbivory to be a threat to the
Neches River rose-mallow at this time. See the Summary of Factors
Affecting the Species section of this final rule for our complete
evaluation.
(26) Comment: The best available information stated that the Texas
golden gladecress and the Neches River rose-mallow are resilient
species.
Our Response: Based on our review of the best available scientific
and commercial data, we concluded that the Texas golden gladecress
exhibits low to moderate resiliency. Although the species has persisted
at several sites in the face of bulldozing, drought, and invasion by
woody species, likely due to its persistent seed bank, and has also
stayed in existence in small sites with small numbers of individuals,
perhaps due to self-fertilization, it has shown no resiliency to
impacts such as excavations (e.g., quarrying) and pipelines. For more
information, see the Determination section of this rule. In the case
for the Neches River rose-mallow, the best available scientific
information indicates that, while reductions in the species' range have
not occurred, there have been significant impacts from habitat
modification and loss that have caused reductions in most, if not all,
of the known Neches River rose-mallow populations. The Neches River
rose-mallow is adapted to highly variable rates of water flow,
including seasonal high and low flows, and occasional floods and
droughts. However, as the habitat is so water-dependent, threats that
could adversely modify its habitat, including invasion from nonnative
and native woody vegetation, hydrological changes, herbicide,
trampling, and drought, can have huge impacts. The Neches River rose-
mallow likely requires high precipitation and flowing water or flood
events to disperse seed (Warnock 1995, p. 20; Scott 1997, p. 8; Reeves
2008, p. 3), and although the Neches River rose-mallow is adapted to
persisting during dry portions of the year, a complete lack of water
can diminish seed production, range expansion, and genetic exchange.
(27) Comment: The Texas golden gladecress is already adequately
protected by co-existing with the federally listed white bladderpod and
collaborations between the Service and several partners.
Our Response: White bladderpod is found at two of the remaining
known Texs golden gladecress population sites (see our response to
Comment 22). Both sites are privately owned with the exception of the
Texas golden gladecress plants that extend onto the Sunrise Road ROW at
Caney Creek Glade Site 1; therefore, absent a Federal nexus, no legal
protections are afforded to either species under the Act. The Chapel
Hill landowner does mow or bush-hog at least once per year to try to
keep woody plants from overrunning this small tract, but this action is
strictly voluntary on his part and not assured into the future.
(28) Comment: The mechanisms and plans provided by the Davy
Crockett NF, the TXDOT, groundwater management areas and conservation
districts, federally protected wetlands, and a number of private
initiatives and agreements all serve to adequately protect the Neches
River rose-mallow species.
Our Response: We agree that the Neches River rose-mallow does
benefit from some protections on USFS and TXDOT lands. As of the
effective date of this rule (see DATES), the Neches River rose-mallow
is a federally listed threatened species. Further, we are publishing a
final rule on designation of critical habitat for the Texas golden
gladecress and the Neches River rose-mallow under the Act elsewhere in
today's Federal Register. Therefore, if a Federal nexus exists for a
project, projects within the species' range or within designated
critical habitat units must avoid jeopardizing the species or adversely
modifying its designated critical habitat.
(29) Comment: Local elected officials were not notified of the
proposed designation during the public comment period. It is crucial
that the Service contacts potentially impacted private landowners,
local elected officials and leaders, and industry in these counties.
Our Response: We made substantial efforts to notify the public and
interested parties, as described here. We announced the opening of the
public comment period on the proposed rule in Nacogdoches, Houston, and
Harrison Counties via newspaper public notices on September 19 and 20,
2012. Within 14 days post-publication of the proposed rule in the
Federal Register, the Service mailed 164 letters to recipients that
included both U.S. senators; the U.S. representative from east Texas;
two State senators and three State representatives for the districts in
question; and the county judges and all four commissioners from each of
the following counties: Sabine, San Augustine, Nacogdoches, Houston,
Cherokee, and Trinity. We also notified, via letter, State officials
including the Texas Governor, State Comptroller, Texas General Land
Office (TGLO) Commissioner, and Executive Directors of Texas Parks and
Wildlife Department (TPWD) and Texas Department of Transportation
(TXDOT). Letters were also sent to staff of interested or affected
agencies (TPWD, Texas Council of Environmental Quality, TXDOT, Texas
Railroad Commission, Texas General Land Office, Texas Forestry Service,
Texas Department of Agriculture, U.S. Department of Agriculture's
Natural Resources Conservation Service, USACE), universities,
conservation organizations and other nongovernmental organizations, and
representatives of the following industries: Glauconite quarries, oil
and gas exploration and production, timber production, and forestry
services. In addition, we sent letters to some landowners, including
private individuals, USFS, and TXDOT.
More specifically with regard to landowners, in September 2011,
approximately 1 year prior to publication of the proposed rule, we sent
letters to 107 entities, including representatives of many of the
agencies or organizations listed above, informing the recipients of our
need to gather and analyze the best available information for our use
in developing a proposed rule to list and designate critical habitat
for both species. We then added any landowner contacts that were given
to us to our notification list. For some sites, landownership was
clarified in file records or through communications with
representatives of other organizations. Furthermore, for the Texas
golden gladecress, we partnered with TPWD in March 2012, to host a
Weches Glades workshop and field tour in San Augustine, to which we
invited four private landowners (two with Texas golden gladecress and
two with white bladderpod populations on their property). As
preparation for the field
[[Page 56042]]
tour, permission to access sites was obtained from these four
landowners. The purpose of the workshop and field tour was to acquaint
landowners, and agency representatives that work with private
landowners, with the glade and outcrop habitats, rare plants, and the
listing process and implications, particularly as it applies to plants.
In addition to these landowners, 24 other individuals were invited to
the workshop, including two San Augustine County commissioners; the
Mayor of San Augustine; the Chairman of the local Soil and Water
Conservation District; and individuals from the Natural Resources
Conservation Service, Texas Forest Service, a private forestry services
company, and a mining company. Of the 28 invitees, 17 attended the
workshop and field tour.
As additional outreach to Neches River rose-mallow landowners, land
managers, and agencies that work with them, TPWD organized a workshop
and 2-day field trip in August 2012. The workshop also furnished an
opportunity to explain the listing process and its applicability for
plants. A pre-field trip workshop allowed information to be presented
to 45 attendees that included the Texas Land Conservancy (owner of the
Neches River rose-mallow Lovelady site) and TXDOT (owner of the ROW
sites along SHs 204 and 94).
On April 16, 2013, the day of Federal Register publication of the
document making available the draft economic analysis and reopening the
comment period for the proposal to list the plants and designate
critical habitat, we emailed letters to 157 people including
representatives of agriculture, timber, oil and gas, and mining
industries; local elected officials from the counties in question;
agency staff that work with landowners; and those landowners for whom
we had email addresses. Within 2 days of publication in the Federal
Register, we also sent 208 letters by mail to State and local elected
officials (including all county judges and commissioners); industry
representatives; scholars; conservation organizations; State, Federal,
and local agencies; and all individual landowners who had been
identified through the past 2 years since our initial information
solicitation in September 2011.
(30) Comment: Multiple State entities expressed concerns that these
listings will hamper economic development. They indicated their belief
that listing could impact agriculture and timber planting operations;
oil and gas operations; and highway construction and maintenance
projects in Nacogdoches, Sabine, and San Augustine Counties. They were
concerned that projects with a Federal component could be delayed or
cancelled in the listed counties. They also indicated concern that
listing could impact ground water management, reservoir construction,
road and bridge projects, and agriculture operations in Cherokee,
Harrison, Houston, Nacogdoches, and Trinity Counties.
Our Response: Under section 4(b)(1)(A) of the Act, we must base a
listing decision solely on the best scientific and commercial data
available. The legislative history of this provision clearly states the
intent of Congress to ensure that listing decisions are ``. . . based
solely on biological criteria and to prevent non-biological criteria
from affecting such decisions . . . ''. Therefore, we did not consider
the economic impacts of listing these species. See our response to
Comment 12.
With respect to effects of listing on highway construction and
maintenance, TXDOT has formally consulted with the Service only once
for the white bladderpod in the 26 years that the plant has been
listed. This formal consultation took place in 2009, for a highway
safety improvement project on approximately 10 miles (16.1 km) of SH
21. The consultation resulted in slight modifications to TXDOT's
original plan for a 4-ft (1.2-m) widening of the shoulder, instead
widening it to 3 ft (0.9 m) for a short distance around a white
bladderpod population. The Service and TXDOT agreed to creation of a
``No Work Area'' around the white bladderpod during construction phases
to protect the plant from foot and vehicle traffic and to prevent any
staging of equipment or materials. Provisions were made for TXDOT to
continue maintenance (mowing) within the No Work Area post-project
during the plant's dormant season (July 1 to August 31). The TXDOT also
agreed to enhance habitat by hydroaxing invading woody vegetation at
three white bladderpod sites on private land as compensation for loss
of one or more plants that could not be avoided. These are the types of
recommendations that are anticipated in the few situations where Texas
golden gladecress occurs in State-maintained ROWs. The TXDOT has
indicated that they do not have major highway construction projects
planned anywhere near the critical habitat within the next 20 years, so
we do not anticipate delays of highway construction projects.
(31) Comment: Although Neches River rose-mallow is considered
extirpated in the SH 230 ROW, in 2012, Laura Baker, a graduate student
at Stephen F. Austin State University, reported seeing Neches River
rose-mallows within the ROW somewhere near the former site (Baker 2012,
pers. comm., in Melinchuk 2012, p. 3). This observation needs to be
verified.
Our Response: We visited the site along SH 230 in Houston County in
2011, and did not find any Neches River rose-mallow plants. This site
was considered extirpated due to herbicide overspray along the ROW.
However, based on this comment, the population could still be present.
Another commenter provided information regarding reintroduced
populations near the cities of Douglass and Chireno, and at the
Pineywoods Native Plant Center, all in Nacogdoches County. These
populations need to be verified as Neches River rose-mallow and not a
hybrid variety.
(32) Comment: The Neches River rose-mallow and the other two co-
occurring Hibiscus species are wetland rather than aquatic plants. They
do not grow in permanently standing water. They grow near permanent or
ephemeral water bodies, and the sites are occasionally flooded. For
most of their life cycle they grow on saturated soils that can become
surficially dry. The proposed rule (77 FR 55973) states that the Neches
River rose-mallow prefers deeper water; it would be more correct to say
that the plants prefer areas near deeper water.
Our Response: In our proposed rule at 77 FR 55973, we state,
``Geographically, these three species [the halberdleaf, crimsoneyed,
and Neches River rose-mallows] can be found within similar habitats,
but the halberdleaf and the crimsoneyed rose-mallows prefer deeper
water and are found along edges of major rivers and streams (Blanchard
1976, pp. 10-14; Poole 2011b, pers. comm.), compared with the [Neches
River] rose-mallow, which is found in side channels and floodplains of
major river drainages.''
Neches River rose-mallow is an endemic east Texas wetland species,
occupying relatively open habitat. Soils are of the Inceptisol or
Entisol orders (Diggs et al.2006, pp. 46, 79) and, although generally
water-saturated, can often be surficially dry. Geographically, the
Neches River rose-mallow and the two other co-occurring Hibiscus
species can be found within similar habitats; however, the Neches River
rose-mallow prefers areas near deeper water, whereas the halberdleaf
and crimsoneyed rose-mallows are found along edges of major rivers and
streams (Blanchard 1976, pp. 10-14; Poole 2011b, pers. comm.).
(33) Comment: The general habitat for the Neches River rose-mallow
is more similar to seasonally flooded river floodplains (Diggs et al.
2006, pp. 103-
[[Page 56043]]
104) rather than the short-leaf or loblolly pine-hardwood forest,
longleaf pine, or loblolly pine forest (77 FR 55973).
Our Response: As stated in the proposed rule, Gould (1975, p. 10)
and Correll and Johnston (1979, p. 1030) described the generic
vegetation community of the Neches River rose-mallow as the Pineywoods
of east Texas. Diggs et al. (2006, pp. 2-3) also describes the generic
geographic area as the Pineywoods; however, this was not mentioned in
the proposed rule. More specifically, Neches River rose-mallow habitat
within the Pineywoods is more accurately classified by Diggs et al.
(2006, pp. 103-104) as ``seasonally flooded river floodplains.''
Natural bottomlands occupy the flat, broad portions of the floodplains
of major rivers and are seasonally inundated with loamy to clayey
seasonally flood and host flood-tolerant species of oak, sweetgum, elm,
swamp tupelo, and red maple (Diggs et al. 2006, p. 103). Stands of
shortleaf, longleaf, and loblolly pine are not occupied by the Neches
River rose-mallow.
(34) Comment: The proposed rule states that flowing water is
required for seed dispersal downstream (77 FR 55974, 55988). However,
research suggests this process has not entirely been investigated.
Warnock (1995) notes that seed dispersal of Neches River rose-mallow is
probably by water, Scott (1997, p. 5) stated that seed dispersal
appears to be entirely water dependent, and Reeves (2008) discusses the
dispersal of Hibiscus moscheutos (including lasiocarpos). The commenter
states that although water-mediated seed dispersal of the Neches River
rose-mallow is highly likely, it is not known that flowing water is
required for seed dispersal downstream.
Our Response: We agree that based on the best scientific and
commercial data available, Neches River rose-mallow seeds are likely to
be dispersed by flowing water. This change is reflected in the
``Habitat'' section for the Neches River rose-mallow of this final
rule, yet this comment did not change our listing determination for the
Neches River rose-mallow.
(35) Comment: Of the four introduced populations of Neches River
rose-mallow, all but the experimental site (which has been manipulated)
have experienced population declines (50 percent in Davy Crockett NF
compartment 20, 90 percent in Davy Crockett NF compartment 16, and 95
percent in Davy Crockett NF compartment 11). Rapidly declining
populations such as those in Davy Crockett NF compartments 16 and 11 do
not appear viable.
Our Response: The Act requires us to determine if the Texas golden
gladecress and Neches River rose-mallow warrant listing based on our
assessment of the five listing factors described in the Act using the
best scientific and commercial data available at the time we conduct a
review of the species. As part of our assessment, we evaluate whether a
threat(s) is causing declines in numbers of individual plants in all
populations or in specific population sites. However, a population's
viability in and of itself, if not influenced by specific threats, is
not a factor considered in our evaluation.
(36) Comment: One commenter noted that several of the population
estimates throughout the proposed rule were not accurate or consistent.
Information pertaining to sites 2, 3, 6, 7, and 8 in Table 4 of the
proposed rule needs to be changed. Site 2 states 78 plants were counted
in 2003, but this should read stems. Site 3 states that 200-250 Neches
River rose-mallow plants were introduced on compartment 20 of the Davy
Crockett NF in 2000; however, the critical habitat section (Critical
Habitat Unit 7) states that 350-400 plants were introduced in 2000. The
actual number introduced is important in evaluating the success of the
reintroduction. Site 8 states several hundred plants were counted in
2001, but this should read several hundred flowers. Site 7, the SH 204
ROW site, has had as many as 75 individuals, not a maximum number of
seven plants.
Our Response: The language in Table 4 pertaining to site 2
(compartment 16 of the Davy Crockett NF) has been updated. Site 2
(compartment 16) and Site 4 (compartment 20) were planted in 2000
(Nemec 2000, p. 3), totaling 700 plants in both units, with about 450
plants in Site 2 and about 200-250 plants in Site 4. Site 6 (SH 204)
has been observed with about 75 plants in 1997, its maximum count to
date, and this change is reflected in this final rule.
(37) Comment: One commenter noted the steep decline in the
reintroduced site in compartment 16 of the Davy Crockett NF where the
population has decreased by 90 percent (from 450 to 43 plants). Whether
the loss of the beaver dam resulted in this drastic decrease needs
further study.
Our Response: See our response to Comment 19.
(38) Comment: In the proposed rule under the heading ``Trampling by
Feral Hogs and Cattle'' (77 FR 55987), it states that because Neches
River rose-mallow habitat is permanently or temporarily flooded, feral
hogs have limited access to the plants. Neches River rose-mallows do
not occur in permanently standing water, although they may grow
adjacent to such sites. Their habitat is only flooded infrequently. For
most of the year, it is surficially dry and easily disturbed by feral
hogs. The commenter also noted feral hog damage of Neches River rose-
mallow (breaking and flattening) at the introduction site in
compartment 20 on the Davy Crockett NF (TXNDD 2012a).
Our Response: National Wetland Inventory (NWI) maps were used to
verify habitat at each Neches River rose-mallow site. Compartment 20
was described on the NWI map as permanently or temporarily flooded
habitat. The Service recognizes that Neches River rose-mallow prefers
areas located near deeper water, generally with temporary not permanent
standing water. The long-term impact on the Neches River rose-mallow
from feral hog damage is unknown. Feral hog presence has been limited
to five Neches River rose-mallow sites with minimal damage to habitat.
The Service considers feral hogs a present threat and one that will
likely continue into the near future. However, at this time, the
severity of impacts to the species is low. This threat does not change
the determination to list the species as threatened versus endangered.
See also our response to Comment 18.
(39) Comment: The listing proposal states that no genetic studies
have been conducted on the Neches River rose-mallow; however, there
have been two such studies by Klips in 1995 and Mendoza in 2004.
Neither study looked at genetic drift, inbreeding, or the possible
threat from hybridization. It seems premature to conclude that small
population size and hybridization are not potential threats.
Our Response: The Service has reviewed Klips (1995, entire) and
Mendoza (2004, entire) and incorporated this information into our
analysis in the Summary of Factors Affecting the Species section of
this final rule. While these studies pertain to genetic analysis, they
do not look at genetic drift, inbreeding, or the possible threat from
hybridization, as the commenter acknowledges. Based on the best
scientific and commercial data available, we do not consider
hybridization or small population size a threat to the species at this
time. See our response to Comment 11 for additional information
regarding this comment.
(40) Comment: Listing of the two plants will have adverse impacts
on the State transportation system other than in instances where they
occur in or immediately adjacent to State-owned
[[Page 56044]]
ROW. Listing will hamper economic development and delay projects that
require section 7 consultations.
Our Response: See our response to Comment 30 above.
(41) Comment: There are existing mechanisms that adequately protect
both species.
Our response: See our response to Comments 22, 27, and 28.
Federal Agency Comments
(42) Comment: The Natural Resources Conservation Service indicated
their willingness to assist landowners and land managers in identifying
those elements that may have a negative or positive impact on the
species.
Our Response: We appreciate the Natural Resources Conservation
Services' (NCRS') willingness to help landowners with actions to
conserve these species. We foresee that NRCS' assistance to landowners
and to the Service will be invaluable in delivering conservation
programs like the Service's Partners for Fish and Wildlife Program that
can help willing landowners plan and implement projects to restore
habitat for both of these plant species.
Public Comments
(43) Comment: One commenter provided information regarding
reintroduced populations near the cities of Douglass and Chireno, and
at the Pineywoods Native Plant Center, all in Nacogdoches County. These
populations have not been verified by the Service or a species expert.
These populations need to be verified as Neches River rose-mallow and
not a hybrid variety.
Our Response: These populations have not been verified by the
Service or species experts. Until such verification, the Service cannot
use this information in our analysis.
(44) Comment: Several commenters expressed their beliefs that these
species have not been fully studied. They indicated that there are
significant concerns with the quality of data and analysis the Service
used for its determination. They believe that the proposal is based
largely on inconclusive reports and vast speculation about operations
thought to affect habitats, existing regulatory mechanisms,
conservation efforts, species populations, and potential threats that
fail to provide any sound scientific foundation on which to justify the
listing of these species. Other commenters assert that the Service does
not have the scientific justification to list these species.
Our Response: See our response to Comment 23.
(45) Comment: As outlined in the 2003 St. Augustine Glades
Conservation Area Plan, TNC, along with other resource professionals,
identified the conservation concerns and challenges for sustaining
populations of the Texas golden gladecress.
Our Response: We were aware of this document and considered this in
our preparation of this determination.
(46) Comment: A commenter recommended that the benefits provided by
conservation efforts currently in place in an area be fully considered.
Our Response: Section 4(b)(1)(A) of the Act requires us to take
into account those efforts being made by a State or foreign nation, or
any political subdivision of a State or foreign nation, to protect such
species. We consider relevant Federal, State, and tribal laws and
regulations when developing our analysis. Regulatory mechanisms may
preclude the need for listing if we determine such mechanisms
adequately address the threats to the species such that listing is no
longer warranted. However, existing regulatory mechanisms are
inadequate to protect these species, and the ongoing conservation
efforts are not sufficient to remove the threats to these species.
Please see ``Other Conservation Efforts'' under ``A. The Present or
Threatened Destruction, Modification, or Curtailment of Its Habitat or
Range'' for the Texas golden gladecress and Neches River rose-mallow in
this final rule.
(47) Comment: Multiple commenters believe that interested parties
should be given sufficient opportunity to review and comment on any
proposal, including review of scientific data from an independent
specialist's economic analysis of the current proposal, before the
Service makes a final decision in this rulemaking. Similarly, any data
provided to Service during future public hearings should also be made
available to the public for review and comment.
Our Response: This information was provided to the public for
review and comment. Please see our response to comment 29 above for a
full description.
(48) Comment: One commenter recommended that any proposal to list a
species should include easily accessible and transparent information
about cited literature. Another commenter noted that Executive Order
13463 directs agencies to provide timely online access to the
rulemaking docket on https://www.regulations.gov, including relevant
scientific and technical findings, in a format that can be easily
searched and downloaded (E.O. 13463, sec. 2(b)). The proposed rule
failed to provide a meaningful opportunity to understand and comment on
the Service's proposal.
Our Response: Executive Order 13463, signed by the President on
April 18, 2008, amends Executive Orders 13389 (Creation of the Gulf
Coast Recovery and Rebuilding Council) and 13390 (Establishment of a
Coordinator of Federal Support for the Recovery and Rebuilding of the
Gulf Coast Region). None of these three Executive Orders directs
Federal agencies to provide timely online access to the rulemaking
docket. We believe the commenter is referring to Executive Order 13563,
``Improving Regulation and Regulatory Review,'' and we believe that we
have met the direction of that Executive Order. For our proposed rule
to list the species and designate critical habitat, we provided the
literature cited bibliography on https://www.regulations.gov when we
published the proposed rule. The proposed rule also stated that
additional tools and supporting information that we developed for that
proposal were available at the Service's field office in Corpus Christi
by appointment or that arrangements could be made to get that
information by calling the field office. For this final determination,
the literature cited bibliography and all tools and supporting
information are available at:
https://www.regulations.gov under Docket No. FWS-R2-ES-
2012-0064,
https://www.fws.gov/southwest/es/ElectronicLibrary/ElectronicLibrary_Main.cfm,
https://www.fws.gov/southwest/es/ClearLakeTexas, and
Texas Coastal Ecological Services Field Office in Corpus
Christi (see ADDRESSES).
(49) Comment: The Service's failure to examine relevant evidence,
explain its assumptions, consider contrary evidence in the studies on
which it relies, identify uncertainties, share the studies it relied
upon, and utilize basic scientific principles in its predictive
analysis is arbitrary, capricious, and not in accordance with the law.
There is no basis in the record to support listing the plants under the
Act.
Our Response: As we are unable to identify from this comment the
specific assumptions or contradictory evidence that the commenter is
referring to, we cannot adequately provide a response to that part of
this comment. We assessed the status of both species using the best
scientific and commercial data available. We obtained this information
by reviewing the candidate assessments that had been done for each
species since they were first determined to be warranted for listing
(in 1975 for the
[[Page 56045]]
Neches River rose-mallow, and in 1997 for the Texas golden gladecress),
using all information in our files, soliciting new information prior to
publication of the proposed rule, as well as during two comment
periods, from a wide variety of knowledgeable entities and individuals,
and using additional sources of information such as peer-reviewed
journals and other publications. We incorporated all substantial
information we received into this final rule, including any new
information regarding the species' status, habitat conditions, and
threats. We believe that we did identify and point out uncertainties
and data gaps. We had to rely on the best scientific and commercial
data available to us, as opposed to collecting new data to fill gaps.
We believe that we have made a sound case for why the Texas golden
gladecress warrants listing as endangered and the Neches River rose-
mallow warrants listing as threatened under the Act. For further
information, see our response to Comment 23.
(50) Comment: The threat to SH 204 ROW by ``water management
strategies'' is speculative. There are no scientific data that
demonstrate the level of hydrological change that would impact the
Neches River rose-mallow; the Service is speculating this threat. Also,
the proposed rule's discussion of the plant numbers for the Neches
River rose-mallow and the impacts of the proposed Lake Columbia project
on this species have not been subjected to rigorous scientific analysis
or discussion. The Service does not report on information from two of
its published reports; specifically plant count information was missing
from 2007. Also, in these reports, plants were determined to be
Hibiscus hybrids; however, this was not mentioned. There is no
explanation of why the Service did not present this readily available
data.
Our Response: Some degree of hydrological change has been seen at
most of the Neches River rose-mallow sites; however, information on
some of the private land sites is lacking. Many wetland species,
including the Neches River rose-mallow, are adapted to highly variable
rates of water flow, including seasonal high and low flows, and
occasional floods and droughts. For example, the Neches River rose-
mallow likely requires high precipitation and flowing water or flood
events to disperse seed (Warnock 1995, p. 20; Scott 1997, p. 8; Reeves
2008, p. 3), and although the Neches River rose-mallow is adapted to
persisting in dry conditions during portions of the year, a complete
lack of water can diminish seed production, range expansion, and
genetic exchange. As Niches River rose-mallow habitat is so water-
dependent, hydrological changes can have huge impacts.
In regards to the SH 204 ROW site, the best scientific and
commercial data available suggest that the construction of the Lake
Columbia reservoir project will divert water downstream, thereby likely
dewatering the site. The agencies involved with the project are still
working on solidifying the project details, and, therefore, we do not
know how much water will remain at this site or if future water
management practices or decisions will allow for seasonal flooding of
water to this site. Please reference the ``Hydrological Changes''
section in this rule for more information on this project and
hydrological impacts to this and other sites.
Summary of Changes From Proposed Rule
There are not any substantial changes from the proposed rule. We
did receive new information regarding the presence of feral hogs at
Neches River rose-mallow sites. Based on this new information, we
determined that feral hogs are a current and continuing threat to the
Neches River rose-mallow, but the severity of the threat is low. We
also received new information about ongoing service line improvements,
including communication, domestic gas, water, sewer, and electric
lines, that were occurring within the Texas golden gladecress's range,
sometimes in highway ROWs. We determined that, because these
improvements may involve excavations of habitat and plants, they could
constitute additional threats to the Texas golden gladecress. These
newly identified threats do not alter our listing determinations.
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533), and its implementing
regulations at 50 CFR part 424, set forth the procedures for adding
species to the Federal Lists of Endangered and Threatened Wildlife and
Plants. Under section 4(a)(1) of the Act, we may list a species based
on any of the following five factors: (A) The present or threatened
destruction, modification, or curtailment of its habitat or range; (B)
overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; and (E) other natural or manmade
factors affecting its continued existence. Listing actions may be
warranted based on any of the above threat factors, singly or in
combination. Each of these factors is discussed below.
Texas Golden Gladecress
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Habitat loss and degradation have been the primary cause of decline
in Texas golden gladecress during the last two decades. Permanent
removal or destruction of habitat by quarrying and pipeline
installation projects has eradicated several populations. Other habitat
alterations that are occurring across the species' range, with
potential to destroy or negatively alter Texas golden gladecress's
habitat, include construction of well pads, buildings, roads, and
poultry production facilities, and service line improvements. A
historic and ongoing major threat to Texas golden gladecress's habitat
is the invasion by nonnative and native shrubs, trees, and vines, and
other weedy species into the formerly open-sun, herbaceous, glade
vegetation communities. Planting of pine plantations can potentially
have negative impacts on the Texas golden gladecress if the spacing of
planted trees puts them in close proximity to occupied outcrops,
resulting in shading and pine leaf litter accumulations in the glade
habitat. Grazing has been implicated as a habitat threat because it is
often associated with the encroachment of undesirable vegetation into
the outcrop habitat, and may lead to trampling of plants. Agricultural
herbicide use has some potential to damage emerging Texas golden
gladecress seedlings. Severe and extended periods of drought,
anticipated to increase with projected changes in the climate, may
negatively affect a given year's reproductive effort by Texas golden
gladecress. These factors will be discussed in more detail below.
Glauconite Quarrying (Mining)
Glauconite, often called ``blue rock'' or ``green rock,'' is used
in San Augustine and Sabine Counties for road construction and
maintenance by county road departments, USFS, and Louisiana Parishes
(McGee 2011, pers. comm.). Glauconite has also been used by the oil and
natural gas industry for roads and well pads, and demand by the oil and
gas industry is high (McGee 2011, pers. comm.). Glauconite is also used
as a component of fertilizer and as an animal feed additive (Godwin
2012, pers. comm., p. 4). A number of commercial glauconite quarries or
mines were in production by 1997, and
[[Page 56046]]
subsequent interest in its use grew because traditional pavement base
materials historically used in this region (iron ore and limestone)
were becoming harder to obtain and more expensive (Button and Little
1997, p. 14). A representative of one mining company with four quarries
in the San Augustine and Sabine County area expressed an opinion that
their mines were sustainable for 15 to 20 years at the current level of
demand (McGee 2011, pers. comm.). The best scientific and commercial
information available does not allow us to make predictions about
future demand for glauconite, and we are unable to project the level of
future quarry development throughout the Texas golden gladecress's
range. Selection of quarry sites can be based on different site
qualities and the variation in the mineral composition of the Weches
Formation across its geographic range. Selection of locations for
glauconite quarries may target areas ``where the glauconite can be seen
on the surface'' (outcrops), although quarries have also been dug on
sites where the glauconite was not visible at the surface (McGee 2011,
pers. comm.).
TNC (2003, p. 9) noted that glauconite quarrying (mining) in glades
destroys habitat and is a significant threat to the Texas golden
gladecress. The majority of known habitat was excavated at three of the
eight historical populations (Caney Creek Glade Sites 2, 6, and 8)
between 1996 and 2011, resulting in open pits at the former habitat
sites. The excavations removed all surface features required by the
gladecress, as well as killing individual plants. The Service has been
denied access to these sites; thus we cannot determine if any habitat
or plants remain on the periphery of the excavated quarries. The last
recorded survey of plants at Caney Creek Glade Site 2 was on March 18,
1988, when the Texas golden gladecress plants were described as growing
on the sloping Weches outcrop that was brush-hogged and burned in 1988.
Using available high-altitude photography taken between 1995 and 2009,
supplemented with aerial photography from August 2010, it appears that
the glade was still intact as of 1995-1996, but that a much larger area
than the original population site was excavated by 2005. As of 2010,
the entire population site and surrounding area looks to be two large,
side-by-side pits or ponds. Based on the total loss of habitat (surface
and subsurface) due to the excavation, over a large portion of the
former population site, we assume that the population was extirpated
here.
The last information on plant numbers and conditions at the Caney
Creek Glade Sites 6 and 8 was collected on March 19 and April 24, 1987.
At that time, Caney Creek Glade Site 6 was recognized as the largest
known viable population of Texas golden gladecress. At this site, the
Texas golden gladecress grew in a former pasture with thousands of
fruiting plants in association with other native glade plants,
including white bladderpod, in shallow bedrock pockets. The Caney Creek
Glade Site 8 consisted of a very small population on a degraded Weches
outcrop, with scattered plants in fruit. Both elements of occurrence
appeared to be eliminated by a large, open-pit quarry in which digging
started after 1996, with the entire area being one large pit by 2009.
The outcrops may actually attract glauconite quarrying interests
because the presence of an outcrop indicates that glauconite is close
to the surface. Glauconite mining can occur throughout the range of
Texas golden gladecress and has the potential to eradicate populations
at sites where quarries are dug. There is no requirement for permits to
develop a quarry, typically there is no Federal nexus, and locations of
future quarries are unknown. Based on our review of the scientific
information, we conclude that excavation of pits for removal of
glauconite, and associated glauconite-quarrying activities, pose a
threat to the Texas golden gladecress across the species' range.
Natural Gas and Oil Exploration and Production
A principal threat to the habitat of Texas golden gladecress is the
removal or destruction of habitat (outcrops and immediate surrounding
land) by pipeline construction or from construction of buildings, well
pads, or roads to access drilling sites directly over habitat. Natural
gas pipeline installation requires trenching and clearing that can
destroy all gladecress habitat and plants within the pipeline ROW. In
addition to the destruction of habitat, excavation could conceivably
alter the hydrology of Texas golden gladecress sites if the lowered
elevation of the excavation, or conversely, the increased ground
elevation of a well pad or other structure, diminishes the amount of
water that can move downslope over ground or through seeps. Adversely
affecting the amount and timing of water delivery could render outcrop
ledges uninhabitable for the species by interfering with the seeping or
pooling action of water on which the species depends.
The loss of habitat and plants in the footprint of well pads and
roads built for natural gas or oil exploration and production is a
continuing threat because there is high potential to affect remaining
glade habitat throughout the species' range. Numerous wells can be seen
from SH 21 between the cities of Nacogdoches and San Augustine, with at
least 30 wells visible along a 20-mile (32-km) stretch of this road
(Loos 2011, pers. comm.; Rodewald 2011, pers. comm.). The materials
brought in to construct well pads and roads can directly cover habitat
and plants, causing partial or total loss of populations. Excavations,
as well as construction activities, that occur upslope of Texas golden
gladecress populations may act to impede movement of water downslope,
thereby interfering with seeping and pooling of water needed by Texas
golden gladecress. Concern about the extent of this threat is elevated
due to our lack of information about potential Texas golden gladecress
populations across the Weches glades where surveys for the species have
not been undertaken, but where natural gas exploration and production
is rapidly proceeding.
The entire known distribution of Texas golden gladecress is
underlain by the Haynesville Shale formation (also known as the
Haynesville-Bossier), recently recognized as a major natural gas source
for the United States. The Haynesville Shale, located at a depth
exceeding 11,000 ft (3,353 m), straddles the Texas-Louisiana border,
and almost 70 percent of its production is from wells located in Texas
(Brathwaite 2009, p. 16). The Haynesville shale covers an area of
approximately 9,000 mi\2\ (23,310 km\2\). A June 2010 map shows the
Haynesville Shale underlying the northwestern quarter of Sabine County,
the entire northern half of San Augustine County, and the southeastern
third of Nacogdoches County (Haynesville Shale Map 2010). Estimates of
the natural gas contained in this formation's reserves indicate that it
could sustain anticipated energy needs for well beyond the next several
decades (Hall 2009, pp. 3-7; Brathwaite 2009, p. 16). Technological
improvements in exploration (3-dimensional seismic surveys), drilling
(horizontal wells), and well completion and stimulation (hydrologic
fracturing) have enhanced the productive capability of natural gas
shales throughout the United States, including the Haynesville Shale.
Natural gas exploration and production has been rapidly expanding
within the Haynesville Shale, from the first significant production in
2005, to major development of the formation in 2009 (Brathwaite 2009,
p. 16). Drilling activity over the entire Haynesville Shale peaked
around 2009 or 2010, when approximately 200 drilling rigs
[[Page 56047]]
were active. As of September 18, 2011, approximately 130 rigs were
actively drilling; the slowdown is attributed to depressed natural gas
prices (Murphy 2011a, p. 3). Even with natural gas prices down, most
companies continue to drill one well per gas unit on the Haynesville
Shale in order to maintain their leases (Murphy 2011a, p. 3). By
September 2011, as many as 1,500 wells had been drilled with many more
anticipated, along with perhaps another 10 years of active drilling on
this formation (Murphy 2011b, pp. 2-3).
The Texas Railroad Commission's online maps (available at https://gis2.rrc.state.tx.us/public/startit.htm) indicate that natural gas (and
some crude oil) gathering and transmission pipelines are found
throughout Nacogdoches County. In San Augustine County, the majority of
existing pipelines are located in the area north of SH 21 and west of
the town of San Augustine, an area of high glade occurrence. To the
east of San Augustine, there are fewer pipelines, but, of those that
are located in this area, several are large gas transmission lines. One
of these big transmission lines lies directly adjacent to the historic
Caney Creek Glade Site 7. Sabine County has several major interstate
pipelines, but fewer gathering and other transmission lines than the
other two counties, and no pipelines near the Sabine County gladecress
site (Texas Railroad Commission 2011).
The Texas Railroad Commission regulates the oil and natural gas
industry in the State of Texas. The Texas Railroad Commission has
detailed information on all existing pipelines, but the agency has no
way to predict future routes for new pipelines or wells; they are
limited to location data found within permit applications (Nunley 2011,
pers. comm.). New pipelines, as well as ones for which routes are being
determined, do not display on the Texas Railroad Commission Web site,
so although we are aware of the impact that pipeline excavations can
have on Texas golden gladecress, we cannot tell where future pipelines
may affect existing populations or suitable habitat.
Loss of Texas golden gladecress habitat and plants is inevitable if
pipelines are routed directly through population sites. Pipeline
installation requires clearing of a path for the pipeline, cutting a
trench in which to lay the pipe, recovering of the trench, and
restoring the ground's surface. Clearing pipeline pathways eliminates
obstacles to construction (NaturalGas.Org 2011, p. 2), which may
include the rocky outcrops supporting the Texas golden gladecress.
Bulldozing the pipeline path likely permanently removes these rocky
ledges and other features, along with the Texas golden gladecress
plants and seedbed. After the pipe is put into the ground and the
trench covered with soil, elevations are restored and the surface is
revegetated, generally using coastal bermudagrass in this region
(Rodewald 2011, pers. comm.). The Simpson Farms Texas golden gladecress
population, located 6 mi (9.7 km) east of the city of Nacogdoches, was
eliminated by a natural gas pipeline that was installed sometime
between August 2010 and October 2011 (date of installation determined
from comparison of successive years of aerial photography). At this
site, the pipeline ROW was approximately 75 ft (23 m) wide, and the
entire area formerly occupied by the Texas golden gladecress was
covered with deposited sediment or piles of cleared brush (Cobb 2011,
pers. comm.). Given the degree of clearing of the ROW and the adjacent
dirt work, the known extent of habitat is now gone, and the entire
population has likely been extirpated (Cobb 2011, pers. comm.). The
Chapel Hill population may also be affected by future pipeline
construction; the route for a future pipeline was being surveyed in
October 2011 (Cobb 2011, pers. comm.). Although this pipeline does not
directly cross the very small population site between the pasture fence
and the road, it does lie parallel to, and just inside of, the fence
line in a pasture where Texas golden gladecress habitat does exist
(Singhurst 2012c, pers. comm.; Singhurst 2012f, pers. comm.).
The current trend over most natural gas shale formations is to
drill multiple wells, when possible, and well pad sizes can vary
accordingly. Well pad sizes in the San Augustine County area range from
several acres to as large as 14 ac (5.67 ha), depending on the number
of wells (Loos 2011, pers. comm.; Allen 2011b, pers. comm.). Although
most oil and gas companies use existing roads, occasionally the
companies need to build new roads, and in these cases the new routes
may go through outcrop areas. The fill for pads and roads could cover
portions of, or potentially entire, glade sites since some of the
glades are so small. Placement of pads or roads upslope of Texas golden
gladecress sites may have the potential to affect downslope movement of
water to outcrop sites (Ritter 2011b, pers. comm.).
In summary, the remaining populations of Texas golden gladecress
and suitable habitat are within areas that are actively being drilled
for natural gas. Plants and habitat have been destroyed by the
construction of pipelines. The three remaining populations as well as
suitable habitat are at risk of being destroyed by construction of
natural gas and oil infrastructure (pipelines, well pads, metering
stations, and roads) that continue to be constructed throughout the
species' range. Exploration and production of natural gas and oil is
anticipated to continue in this area for at least the next decade.
Texas golden gladecress and its habitat may be directly impacted by the
construction of pipelines and other infrastructure, and indirectly by
altering the hydrology near occupied sites and suitable habitat. Based
on our review of the scientific information, we conclude that natural
gas and oil development is a threat to Texas golden gladecress.
Residential and Commercial Construction
Although residential and commercial construction was listed in the
species' candidate assessments as a potential threat, there is no
evidence that this type of disturbance has directly affected Texas
golden gladecress populations. Historically, site selection for
building homes and businesses in the town of San Augustine may have
taken advantage of the open aspect of the glades; Leavenworth described
the area in which he originally collected the species (vicinity of the
town of San Augustine) as ``prairies'' (Bridges 1988, p. II-5).
However, information about former glades in the area is lacking, as is
documentation that the Texas golden gladecress was present where
buildings are currently located. Neither San Augustine nor Sabine
Counties are experiencing rapid human population growth; San Augustine
County saw a 0.9 percent decline in population from 8,946 to 8,865
between 2000 and 2010, while Sabine County had a modest increase of 3.5
percent (10,469 to 10,834) (U.S. Census Bureau 2010a, b), suggesting
that residential and associated commercial development does not
constitute a high level of threat to habitat throughout the species'
range. However, service improvements for existing homes and businesses,
including installation of service lines for communications, electric
power, water, sewer, and domestic gas are ongoing and do have the
potential to occur in Texas golden gladecress habitat (Walker 2012,
pers. comm., p. 1). Because water, sewer, and gas lines entail
excavations to lay pipe, these activities could have similar
consequences to installing natural gas and oil pipelines if the lines
pass through an occupied outcrop. Electric power structures in this
area are
[[Page 56048]]
generally above-ground poles and lines that may be installed, or
maintained, in highway ROWs. Although Texas golden gladecress habitat
and plants may potentially be impacted by pole placement, the small
project footprint, limited to the pole installation, may mean that the
small Texas golden gladecress sites could be avoided by moving pole
locations a few feet to either side of an outcrop. In those cases where
new power lines are built outside of established ROWs, Texas golden
gladecress populations might be damaged during clearing of habitat by
vehicles and heavy equipment traversing a glade. However, there is also
potential that clearing of woody vegetation out of invaded glades may
reopen them to the point that the Texas golden gladecress could show a
positive response.
Proliferation of poultry farms was also listed as a potential
threat to Texas golden gladecress habitat. Building poultry production
houses and associated facilities would cover Texas golden gladecress
habitat in the same manner as would residential or other types of
commercial construction. Aerial photography from November 2011 (Google
Earth, 2011) shows 21 poultry farms within the Texas golden
gladecress's range (the approximate zone of the Weches Formation) in
Sabine and San Augustine Counties. Of the 21 total, 18 are located on
the San Augustine County Weches Formation. None of the existing farms
is adjacent to any of the known population locations, and we are unable
to determine if any Texas golden gladecress habitat or plants were lost
when these production facilities were built. Among the characteristics
in east Texas that make a site desirable for poultry production are
long, flat stretches of ground with a good, solid hardpan as opposed to
rocky outcrops on slopes, on the tops of ridges, or in low-lying areas
(Ritter 2012, pers. comm.), such as those occupied by the Texas golden
gladecress. This site-selection preference means that poultry producers
would most likely avoid Texas golden gladecress habitat. In the last 2
years, most of the poultry farm construction has taken place in
counties north of San Augustine and Sabine, and the only activity in
the Weches Formation zone has been renovations to existing farms
(Ritter 2012, pers. comm.). The construction of poultry farms is not
considered a threat to Texas golden gladecress because poultry farm
site selection does not appear to have significant overlap with Texas
golden gladecress habitat.
Roads
Two of the three extant Texas golden gladecress populations, Geneva
and Caney Creek Glade Site 1, extend into ROWs managed by TXDOT. The
third confirmed population at Chapel Hill is located on a small tract
adjacent to a county road and is not considered to be in a road ROW. In
the 1990s, a road project impacted the portion of the Caney Creek Glade
Site 1 population that occurred in the SH ROW when Sunrise Road was
widened and straightened (Singhurst 2012g, pers. comm.); however, not
all plants were destroyed. Review of a 2011 list of TXDOT-planned
projects did not show any future road improvements or expansions near
known Texas golden gladecress population sites. Based on the best
scientific and commercial information available, we conclude that new
road construction or improvements to the existing roads does not pose a
threat to the two Texas golden gladecress populations that occur within
ROWs, or to the third population that does not.
Invasive Species
A major stressor to the habitat of Texas golden gladecress is the
ongoing invasion of nonnative and native shrubs, trees, and vines into
the formerly open-sun, herbaceous, glade vegetation communities. This
woody, weedy plant invasion is occurring on at least a portion of all
three remaining population sites. The historic Caney Creek Glade Site 7
appears, from 2010 aerial photography, to be almost 100 percent
overgrown with woody vegetation.
Glades in most parts of the United States are declining due to
grazing, fire suppression, and the subsequent invasion by woody
vegetation. In presettlement times, glades were maintained by periodic
fires and browsing of woody vegetation by white-tailed deer (Odocoileus
virginianus) and elk (Cervus canadensis). This natural disturbance
regime changed over the last century due to active fire suppression and
diminished numbers of browsers reduced by hunting pressure (Rossiter
1995, p. 2). Although the harsh environment of glades helps to preclude
tree establishment, without disturbance such as fire, woody plants will
invade (Hartman 2005, p. 4). The exclusion of fire has allowed
encroachment of trees, shrubs, vines, and other woody plants into glade
communities (Borland 2008, p. 3).
As woody plants mature, they produce canopies that reduce the
amount of sunlight reaching the ground. Sun-loving plants like Texas
golden gladecress that are adapted to hot, dry sites do not tolerate
shade well. Research conducted in Missouri's cedar glades showed that
herbaceous plant production rapidly declined when red cedar cover
exceeded more than one third of a glade's area (Rossiter 1995, p. 3). A
combination of reduced sunlight (shading) and increased leaf litter can
act to suppress herbaceous species (Hartman 2005, p. 2). These types of
changes in glades that were historically hot and dry can contribute to
cooling of the ground and enhancing of moisture content. Wetter, cooler
conditions during traditionally hot, dry summer months may be counter-
productive for sun-loving glade species by encouraging invasion by cool
season vegetation and exotic species. Buildup of a deeper organic layer
can also facilitate the establishment of woody plants that results in
further shading of the ground (Hartman 2005, p. 2).
Invading species can also compete directly with Texas golden
gladecress for water and nutrients. Interspecific competition has been
noted as potentially causing reduction in the extent of the root system
in several small outcrop plant species, thereby reducing their nutrient
uptake (Baskin and Baskin 1988, p. 836). Shading further stresses the
herbaceous layer, including the Texas golden gladecress. In Missouri,
stressed glade communities were more prone to invasion from invasive
species like Schedonorus phoenix (tall fescue), Sericea lespedeza
(Chinese bushclover), and Rosa multiflora (multiflora rose) (Hartman
2005, p. 4). On Texas' Weches glades, Carr (2005, p. 2) reported tall
fescue at the Chapel Hill site, and Macartney rose was listed as a
major invading species in pastures throughout the range of Texas golden
gladecress. The Weches outcrops that parallel SH 21 appear to support
the heaviest Macartney rose infestation in San Augustine County (Ritter
2011a, pers. comm.). A 1995 report by the Service's Clear Lake
Ecological Services Field Office described known white bladderpod
sites, including several with Texas golden gladecress, all of which
needed active management to preclude invasion by woody shrubs (Nemec
1996, p. 1).
Texas golden gladecress habitat has been documented since the 1980s
to be affected by an accelerated succession from open, herbaceous
Weches outcrops to dense shrub thickets and closed canopy woodlands
(Service) 1992, p. 7; Carr 2005, p. 2; Nemec 1996, p. 4). The most
serious invaders are included in Table 5. Encroachment of these species
is thought to suppress the less
[[Page 56049]]
competitive components of the community like Texas golden gladecress
and white bladderpod (TNC 2003, p. 4). Some of these invasive species
can grow on the shallow outcrop soils, while others can invade open
space around the edges of the outcrop ledges (Service 1992, p. 7). Some
of the native invading species are likely controlled by occasional
wildfire under natural conditions. More serious are the introduced
invaders, including the small hop clover that can cover Weches outcrops
and eliminate other vegetation. The introduced shrubs, including
Macartney rose and Japanese honeysuckle, will invade open space,
including Texas golden gladecress habitat (Service 1992, p. 7).
Table 5--Primary Invasive Species Found in Texas Golden Gladecress
Habitat
------------------------------------------------------------------------
Scientific name Common name
------------------------------------------------------------------------
Nonnative Species
------------------------------------------------------------------------
Rosa bracteata......................... Macartney rose.
Lonicera japonica...................... Japanese honeysuckle.
Stellaria media........................ chick-weed.
Bromus japonicus....................... Japanese brome.
Kummerowia striata..................... Japanese bush-clover.
Ligustrum japonicum.................... Japanese privet.
Melilotus indicus...................... sour clover.
Cynodon dactylon....................... coastal bermudagrass.
Trifolium dubium....................... small hop clover.
------------------------------------------------------------------------
Native Species
------------------------------------------------------------------------
Andropogon virginicus.................. broomsedge.
Plantago virginica..................... pale-seeded plantain.
Euphorbia sp........................... spurge.
Frangula caroliniana................... Carolina buckthorn.
Rhamnus lanceolata..................... lanceleaf buckthorn.
Crataegus crus-galli................... hawthorn.
Crataegus spathulata................... hawthorn.
Prunus mexicana........................ Mexican plum.
Viburnum rufidulum (=prunifolium)...... rusty blackhaw.
Rhus glabra............................ smooth sumac.
Ulmus alata............................ winged elm.
Berchemia scandens..................... Alabama supplejack.
Cissus incisa.......................... ivy treebine.
------------------------------------------------------------------------
The three extant Texas golden gladecress sites have shrubs and
trees encroaching into formerly open glade habitat. At the Chapel Hill
site, Carr (2005, p. 2) noted that 13 scattered pines within a 6,000-
ft\2\ (557-m\2\) area produced a total canopy coverage of less than 10
percent of site, but indicated that future shading effects when the
pine trees reach maturity might prove detrimental. At this same site,
other woody plants were controlled, but not eliminated, by regular
shredding (Carr 2005, p. 2).
Texas golden gladecress does show some ability to persist at sites
that have been overrun by woody vegetation. At the Geneva site, the
area with the Texas golden gladecress was bulldozed, and although the
site was reported as destroyed, the species reappeared within several
years. At the Chapel Hill site, brush removal actions to benefit white
bladderpod also resulted in the reappearance of the Texas golden
gladecress after its apparent absence for 10 years. This suggests that
the Texas golden gladecress's seed bank may be able to remain viable
over extended time periods even though the habitat is overgrown by
woody species.
Fire suppression is considered a threat to the continued integrity
of the native plant communities of the Weches glades because lack of
fire contributes to woody and weedy native and nonnative plants being
able to more quickly overtake the open glade areas. TNC's Area
Conservation Plan for the San Augustine Glades indicated that fire
suppression in the Coastal Plain Carbonate Glades (another reference
for the Weches glades) constituted a high level of threat (The Nature
Conservancy 2003, p. 9) and that the fire frequency was ``fair to
poor''; the ideal frequency being burns occurring every 5 to 10 years.
For future viability and biodiversity health in the glades, the plan
said that fire processes should be restored or simulated, where
feasible (The Nature Conservancy 2003, p. 8), and categorized
development and implementation of fire management and invasive species
plans with partner landowners as a top priority conservation strategy
(The Nature Conservancy 2003, p. 13). TNC's plan also stated that
seasonal burns could create habitat conditions allowing establishment
and expansion of white bladderpod populations by triggering germination
and reducing completion from woody invasives, and referred to ``limited
data'' indicating that burns conducted July through October (non-bloom
period) are the most beneficial for the bladderpod. This plan also
indicted that this is probably true for the Texas golden gladecress.
Although information about the direct effects of prescribed burns
on Texas golden gladecress is not available, Dr. Michael Warnock did
conduct experimental burns at Caney Creek Glade Site 6 in the mid-1990s
to determine the impacts on white bladderpod. His experimental burns
did result in white bladderpod showing a positive reproductive
response. However, Dr. Warnock did not list the Texas golden gladecress
in his final report, and did not mention anything about its response to
the experimental burn (Warnock 1992, entire). The TXNDD's element of
occurrence records include descriptions of habitat conditions,
including mention of winter burns, at a time when the Texas golden
[[Page 56050]]
gladecress was present (in fruit) at two historic Texas golden
gladecress sites. At Caney Creek Glade Site 2, Texas golden gladecress
was last observed in March 1988, when the site was described as being
brush-hogged and burned that same year. In 1988, at the Caney Creek
Glade Site 7, part of the Weches formation glade area below a shrubby
slope was in part burned that winter (or early spring), and the Texas
golden gladecress itself was described as being locally abundant in a
very small area on a seepy, gravelly glade (TXNDD 2012b, pp).
Bermudagrass, ryegrass, and bahiagrass are nonnative grasses that
have been documented as occurring at some white bladderpod and Texas
golden gladecress sites. Nemec (1996, p. 4) described bermudagrass as
among the most serious invaders of white bladderpod and Texas golden
gladecress habitat. Carr (2005, p. 4) listed ryegrass (although he
described it as Lolium multiflorum (English rye)) as a common grass
component at the Chapel Hill Site in spring 2005. George (1987, pp. 26-
36) found bermudagrass, bahiagrass, and perennial ryegrass at San
Augustine County glade sites where he assessed the herbaceous
vegetation community. Using ``importance values'' for plant species
that were calculated by summing the relative density and the relative
frequency of the species (with a value of 1 being highest or most dense
and most frequent), he found bermudagrass, ryegrass, and bahiagrass to
rank in importance as 38, 53, and 69 (respectively) of 80 species at
site 1; while ryegrass, bermudagrass, and bahiagrass ranked as 13, 17,
and 23 in importance (respectively) out of a total of 75 species at
site 2. Interestingly, at site 3, which was the sole site with Texas
golden gladecress present, only ryegrass was found; the other two
species were absent. Some of the differences between the three sites
(as described by George 1987, pp. 26-36) may have contributed to the
presence of all the invasive grasses at sites 1 and 2, where they
varied with respect to their frequency and density. Site 3 (where Texas
golden gladecress occurred) was the rockiest and most fossiliferous of
the three sites, with soil and a gravel-like substrate containing many
small rocks. Sites 1 and 2 appeared to include more areas of deeper,
more developed soil. Site 3 was the wettest in the spring and the
driest in the summer and fall, due to rapid drying of the thin soil.
George (1987, pp. 26-36) postulated that the thin, rocky soils of Site
3 were probably a limiting factor that helped to explain the generally
lower densities of most of the plants at the site.
George (1987, pp. 26-36) also described a seasonality component to
the vegetation growth on the Weches glades. This seasonality may help
to keep the habitat conditions suitable for the Texas golden gladecress
even if bermudagrass, bahiagrass, and ryegrass are present. He noted
that the spring was dominated by a sequence of diverse annual forbs,
and as the summer progressed, rainfall diminished, the soil dried out,
and the flora became very sparse. The grasses exhibited large growth
spurts in September and dominated all three sites; however, this time
of grass dominance (summer and fall months) is the time of year when
Texas golden gladecress is not present aboveground. Therefore,
seasonality of growth should help to somewhat ameliorate competition
between the grasses and the annuals on the outcrops.
With regard to ROWs, Texas golden gladecress does extend into
highway ROWs at several sites. Coastal bermudagrass and bahiagrass are
included in mixtures used to re-seed ROWs in the east Texas area (Adams
2013c, pers. comm). Bahiagrass is a deep-rooted perennial adapted to a
wide range of soils. It spreads via stolons and rhizomes, in addition
to being a prolific seed producer. Bahiagrass is most productive on
sandy soils with a pH of 5.5 to 6.5 (Houck 2009, p. 1). These qualities
would seem to contraindicate bahiagrass colonizing and persisting on
the parts of the outcrop where Texas golden gladecress grows, since
bahiagrass does not share an affinity for the thin, rocky, or
nonexistent soils under the Texas golden gladecress.
Ryegrasses grow best on fertile, well-drained soils; however, they
can also grow on soils where conditions are too wet at certain times of
the year to support other grasses because ryegrass is a heavy water
user (Hall 1992, p. 1). Soil pH for optimum ryegrass production is
between 6.0 and 7.0 (Hall 1992, p. 3), so it may be able to tolerate
the alkalinity of the Weches outcrops. Perennial ryegrass requires a
dormancy period of cool temperatures before the photoperiod can induce
flowering, and it normally produces seed heads during late spring (Hall
1992, p. 1). This timing of growth and reproduction may be offset
enough to help to minimize competition if and when ryegrass does grow
onto Texas golden gladecress habitat.
Bermudagrass is a vigorous, stoloniferous grass that can rapidly
invade cultivated land in areas of high rainfall or irrigation (Duble
2013, p. 1). Bermudagrass has a fibrous, perennial root system with
vigorous, deep rhizomes. Root production and dieback is reported to be
especially high in the spring when shoot production begins. Soil
temperatures above 65 degrees Fahrenheit ([deg]F) (18.3 degrees
Centigrade ([deg]C)) are required for significant growth of rhizomes,
roots, and stolons, with the optimum soil temperature for root growth
around 80 [deg]F (27 [deg]C) (Duble 2013, p. 2). Bermudagrass has the
capability of surviving extreme droughts and produces seed heads under
stress conditions (Duble 2013, p. 3). This invasive grass can grow well
on a wide variety of soils from heavy clays to deep sand, as long as
fertility is not limiting. It can tolerate both acid and alkaline soil
conditions and salinities. Bermudagrass does not tolerate poorly
drained sites like compacted soils and heavy clays (Duble 2013, p. 6).
Some qualities of bermudagrass, like its growth and spread via stolons
and shoot production at nodes, along with its tolerance of varying pH
conditions, might enhance its ability to invade the Weches outcrop
habitats, and indeed it has been noted as a significant invader at some
outcrop sites. However, its lack of tolerance for poor drainage might
preclude it from the portions of the outcrop favored by the Texas
golden gladecress. Also, its soil temperature requirements for growing
periods may offset its season of growth and reproduction from that of
the Texas golden gladecress.
Nonnative and native woody species, including woody shrubs, vines,
and trees, continue to degrade Texas golden gladecress's habitat across
the species' entire range. This threat is significant for the species
because it is ubiquitous and has led to declines in, or disappearance
of, Texas golden gladecress populations, along with altering the
species' habitat. Based on our review of the scientific and commercial
data available, we conclude that invasion of woody and weedy nonnative
and native plants into Texas golden gladecress habitat is a threat
across its range. We recognize the potential for bermudagrass,
bahiagrass, and ryegrass to impact the habitat of the Texas golden
gladecress, especially in those situations where these grasses are
deliberately planted nearby to Texas golden gladecress populations.
However, there are characteristics of each of the three that may help
limit competition between these nonnative plants and the Texas golden
gladecress, at least on those Texas golden gladecress sites that have
sufficient outcrop rock ledge or rock face that separate the Texas
golden gladecress
[[Page 56051]]
from the deeper soils needed by the grasses. Based on this information,
we do not consider these specific species a threat at this time. In the
future, if these grasses are shown to impact the Neches River rose-
mallow or Texas golden gladecress, we will work with the appropriate
agencies and industries to address these impacts.
Habitat Damage Associated With Grazing
Grazing has been implicated as a habitat threat because it can
facilitate the encroachment of undesirable vegetation into the outcrop
habitat, and because it may lead to trampling of plants and soil
compaction. Historically, the introduction of grazing livestock into
east Texas, coupled with heavy grazing pressure, adversely impacted
glade sites by facilitating the spread of invasive woody plants, and
potentially trampling native plants. Acting in concert with fire
suppression, heavy grazing pressure may have accelerated conversion of
the grassy prairies and herbaceous glades to the dense, thorny masses
of vegetation seen at many sites today (Nemec 1996, p. 4; Service 1992,
p. 7). Overgrazing of Texas golden gladecress habitat can promote
invasion by woody species and enhance competition on the glade from
herbaceous weeds like pale-seeded plantain, Japanese brome, and spurge
(Service 1992, p. 7). Grazing livestock serve as a source of introduced
species' seeds as well as supplying nutrients for competitive native
weedy species. Grazing animals can also encourage unpalatable invasive
species like Macartney rose to move into areas where more preferred
natives have been grazed out (Bridges 1988, p. II-35). The negative
impacts to Texas golden gladecress habitat from woody plant invasion
are detailed in the ``Invasive Species'' section.
There is no documentation of Texas golden gladecress plants being
lost due to trampling. Potential does exist for this to happen, for
example, at the Geneva Site, where Texas golden gladecress plants have
been observed growing directly adjacent to and inside the fence where a
cow trail is evident. Loss of plants in this small area has not been
confirmed, and the larger part of this population grows in the SH 21
ROW, where no grazing takes place, so it is unlikely that trampling at
this site truly constitutes a threat to the species. Grazing also
occurs within the fenced private portions of the other two remaining
Texas golden gladecress population sites (Caney Creek Glade Site 1 and
Chapel Hill), where individual plants may be subject to trampling if
they are growing directly in cattle trails.
Grazing does occur on portions of the three extant population
sites, but we do not have information to show that grazing has
destroyed Texas golden gladecress habitat or plants. Based on our
review of the best scientific information, we conclude that the direct
effects of grazing are not a threat to Texas golden gladecress.
Land Conversion for Agriculture and Silviculture
Another potential habitat threat is conversion of Weches glade
outcrops to nonnative grass pastures or conversion of existing pasture
lands that may contain viable outcrops to pine tree plantations. Over
the last 200 years, most of the native vegetation communities of east
Texas were dramatically altered by human activities as the region was
logged and extensively cultivated (Diggs et al. 2006, p. 76). Due to
widespread land use changes throughout the entire range of the Texas
golden gladecress, and the fact that the glade areas were always
somewhat small and surrounded by forest, there is a high likelihood
that some glades were negatively affected by past agricultural and
silvicultural land cover conversions (Service 1992, p. 7). At least one
Texas golden gladecress population was described as being lost to this
type of land use change during the 1980s (Turner unpubl. Data, in TNC
2003, p. 2).
Conversion of native vegetation communities to pasture or row crop
in the region is much less common now. The Weches outcrops are not
considered desirable substrate for planting to pasture, as landowners
are not interested in deep plowing, breaking up, or dragging out rocks
(Ritter 2011a, pers. comm.). The ``Redland'' soils that are exposed in
the Weches outcrops are thin and rocky. The Natural Resources
Conservation Service recommends avoiding these soils because there are
not practical conservation practices for these types of sites (Ritter
2011a, pers. comm.). The more prevalent land use change now is from
pasture to tree plantation (Ritter 2011a, pers. comm.). Within the last
few years, many Sabine and San Augustine County landowners have shifted
from grazing to timber planting (Ritter 2011a, pers. comm.). Most
timber planting consists of Pinus taeda (loblolly pine) and Pinus
palustris (longleaf pine), planted on 8-10 ft (2.4-3 m) centers.
Although landowners will likely avoid planting directly onto Weches
outcrops because these rocky soils will not support trees, it is
conceivable that the spacing between plantings would allow trees to be
planted near the edges of outcrops (Ritter 2011a, pers. comm.; Ritter
2012, pers. comm.). As these trees mature, their canopies may
potentially cause shading problems on glade areas (see ``Invasive
Species'' section for explanation of negative effects of shading). For
example, it appears that former habitat adjacent to the Chapel Hill
site may be planted, in part, to rows of trees.
In addition to shading, pine tree plantings may also result in
production of large amounts of pine needle litter that could accumulate
in small glade openings near the trees. Where a mid-story of trees
develops, light may be blocked from reaching the ground level by upper-
canopy and mid-story shading; with a subsequent build-up of leaf
litter, the herbaceous species can be suppressed. In the face of fire
suppression, Missouri glades became choked with litter that kept the
ground moister and cooler, leading to replacement of the sun-loving
natives by invading cool-season vegetation and exotic species (Hartman
2005, pp. 2-4). The decomposition of pine leaf litter also facilitates
the germination of pines as the soil deepens within the glade (Walker
2012, pers. comm., p. 1).
Current data do not suggest that the establishment of pine tree
plantations is a threat to the species. However, if in close proximity
to occupied glade openings, this may potentially cause problems for
Texas golden gladecress. If this becomes an issue in the future, we
will consider it in our recovery planning and implementation.
Herbicide Use
The candidate assessments for Texas golden gladecress list
herbicide use in highway ROWs and for agricultural purposes as a
potential threat to the species because of the plant's occurrence
within highway ROWs and in pastures. Herbicide use to maintain highway
and county road ROWs has the potential to destroy the small
subpopulations that exist in the TXDOT ROWs at the Geneva and Caney
Creek Glade 1 sites. If timing of the herbicide application coincides
with the growing and reproductive period of the year for the Texas
golden gladecress, all individuals that are growing in the ROW might be
extirpated if the herbicide contacts all Texas golden gladecress
individuals in these small sites. Herbicide exposure from highway and
county road maintenance would affect only a small portion of two extant
sites, and recent information suggests that use of herbicides for State
and county roads in this area is not a widespread practice
[[Page 56052]]
(Adams 2011b, pers. comm.; Hunter 2011, pers. comm.). We do not have
documentation of negative impacts to the species from herbicide
applications for road maintenance. The TXDOT uses herbicides only on an
``as needed'' basis to eliminate encroaching woody plants or along the
edges of the road pavement (Adams 2011b, pers. comm.). San Augustine
County does not use herbicides for county roadside maintenance due to
costs (Hunter 2011, pers. comm.).
With regard to agricultural herbicide use in San Augustine and
Sabine Counties, the Natural Resources Conservation Service has a
program to assist landowners with Macartney rose control using
Grazon[supreg] P+D herbicide. This program involves a 3-year approach--
broadcast spraying from a tractor during the first 2 years, followed by
individual plant treatments in the third year. Grazon[supreg] P+D has
active ingredients of picloram and 2,4-D (dichlor) and can persist in
some soils for months and act as a preemergent, killing germinating
seedlings. In an appendix to TNC's Conservation Area Plan for the San
Augustine Glades (The Nature Conservancy 2003, pp. 30-31), it is one of
several herbicides identified as potentially harmful to the Texas
golden gladecress and white bladderpod if used near their habitats.
Management recommendations include avoiding use of this herbicide
within 200 yards (yd) (183 m) of areas described as habitat within the
region, along with limiting timing of use to spot treatments only
between July 1 and August 30. Because Macartney rose is infesting the
region of the Weches outcrops, and since this exotic invader is capable
of establishing itself in Weches glades and has been noted as occurring
at Texas golden gladecress population sites, it is reasonable to assume
that some areas of glade habitat are included in these treatment
programs. Thus, although control of Macartney rose would likely benefit
the Texas golden gladecress in the long term, application of a pre-
emergent herbicide has the potential to eliminate the Texas golden
gladecress altogether if it stays in the soil long enough to kill
emerging seedlings. We have no evidence that this type of application
has affected Texas golden gladecress populations to date.
Based on our review of the scientific information, we conclude that
using preemergent herbicides such as Grazon[supreg] P+D that persist in
the soil for brush control constitute a threat to Texas golden
gladecress's emerging seedlings.
Climate Change
Our analyses under the Act include consideration of ongoing and
projected changes in climate. The terms ``climate'' and ``climate
change'' are defined by the Intergovernmental Panel on Climate Change.
The term ``climate'' refers to the mean and variability of different
types of weather conditions over time, with 30 years being a typical
period for such measurements, although shorter or longer periods also
may be used (Intergovernmental Panel on Climate Change 2007a, p. 78).
The term ``climate change'' thus refers to a change in the mean or
variability of one or more measures of climate (for example,
temperature or precipitation) that persists for an extended period,
typically decades or longer, whether the change is due to natural
variability, human activity, or both (Intergovernmental Panel on
Climate Change 2007a, p. 78).
Scientific measurements spanning several decades demonstrate that
changes in climate are occurring, and that the rate of change has been
faster since the 1950s. Examples include warming of the global climate
system, and substantial increases in precipitation in some regions of
the world and decreases in other regions. For these and other examples,
see Intergovernmental Panel on Climate Change 2007a, p. 30 and Solomon
et al. 2007, pp. 35-54, 82-85. Results of scientific analyses presented
by the Intergovernmental Panel on Climate Change show that most of the
observed increase in global average temperature since the mid-20th
century cannot be explained by natural variability in climate, and is
``very likely'' (defined by the Intergovernmental Panel on Climate
Change as 90 percent or higher probability) due to the observed
increase in greenhouse gas (GHG) concentrations in the atmosphere as a
result of human activities, particularly carbon dioxide emissions from
use of fossil fuels (Intergovernmental Panel on Climate Change 2007a,
pp. 5-6 and figures SPM.3 and SPM.4; Solomon et al. 2007, pp. 21-35).
Further confirmation of the role of GHGs comes from analyses by Huber
and Knutti (2011, p. 4), who concluded it is extremely likely that
approximately 75 percent of global warming since 1950 has been caused
by human activities.
Scientists use a variety of climate models, which include
consideration of natural processes and variability, as well as various
scenarios of potential levels and timing of GHG emissions, to evaluate
the causes of changes already observed and to project future changes in
temperature and other climate conditions (for example, Meehl et al.
2007, entire; Ganguly et al. 2009, pp. 11555, 15558; Prinn et al. 2011,
pp. 527, 529). All combinations of models and emissions scenarios yield
very similar projections of increases in the most common measure of
climate change, average global surface temperature (commonly known as
global warming), until about 2030. Although projections of the
magnitude and rate of warming differ after about 2030, the overall
trajectory of all the projections is one of increased global warming
through the end of this century, even for the projections based on
scenarios that assume that GHG emissions will stabilize or decline.
Thus, there is strong scientific support for projections that warming
will continue through the 21st century, and that the magnitude and rate
of change will be influenced substantially by the extent of GHG
emissions (Intergovernmental Panel on Climate Change 2007a, pp. 44-45;
Meehl et al. 2007, pp. 760-764, 797-811; Ganguly et al. 2009, pp.
15555-15558; Prinn et al. 2011, pp. 527, 529). (See IPCC 2007b, p. 8,
for a summary of other global projections of climate-related changes,
such as frequency of heat waves and changes in precipitation. Also see
Intergovernmental Panel on Climate Change 2011 (entire) for a summary
of observations and projections of extreme climate events.)
Various changes in climate may have direct or indirect effects on
species. These effects may be positive, neutral, or negative, and they
may change over time, depending on the species and other relevant
considerations, such as interactions of climate with other variables
(for example, habitat fragmentation) (Intergovernmental Panel on
Climate Change 2007a, pp. 8-14, 18-19). Identifying likely effects
often involves aspects of climate change vulnerability analysis.
Vulnerability refers to the degree to which a species (or system) is
susceptible to, and unable to cope with, adverse effects of climate
change, including climate variability and extremes. Vulnerability is a
function of the type, magnitude, and rate of climate change and
variation to which a species is exposed, its sensitivity, and its
adaptive capacity (Intergovernmental Panel on Climate Change 2007a, p.
89; Glick et al. 2011, pp. 19-22). There is no single method for
conducting such analyses that applies to all situations (Glick et al.
2011, p. 3). We use our expert judgment and appropriate analytical
approaches to weigh relevant information, including
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uncertainty, in our consideration of various aspects of climate change.
As is the case with all stressors that we assess, even if we
conclude that a species is currently affected or is likely to be
affected in a negative way by one or more climate-related impacts, it
does not necessarily follow that the species meets the definition of an
``endangered species'' or a ``threatened species'' under the Act. If a
species is listed as endangered or threatened, knowledge regarding the
vulnerability of the species to, and known or anticipated impacts from,
climate-associated changes in environmental conditions can be used to
help devise appropriate strategies for its recovery.
The climate in Texas has shown a long-term gradual warming trend;
pollen, plant macrofossils (fossils large enough to be seen without a
microscope), packrat middens (ancient ``garbage piles'' left by rodents
in the genus Neotoma), and other evidence show substantial climate
changes in Texas over the past 15,000 years (end of the last glacial
period), when the mean annual air temperature was 9 [deg]F (5 [deg]C)
cooler than present (Diggs et al. 2006, p. 73). The Texas climate is
considered highly variable, with seasonal precipitation patterns that
dramatically increase from west to east, and temperatures that increase
from north to south (Nielsen-Gammon 2008, p.1). Climate models predict
increased temperatures, and concurrent increased evapotranspiration,
and decreased regular precipitation and soil moisture in Texas (Diggs
et al. 2006, p. 73), all of which would have negative implications for
Texas golden gladecress. Based on a climate model developed by the
United Kingdom Hadley Center (HadCM2), temperatures in Texas could
increase by 3 [deg]F (1.7 [deg]C) in spring (range of 1-6 [deg]F (0.6-
3.3 [deg]C)) and about 4 [deg]F (2.2 [deg]C) in other seasons (with
range of 1-9 [deg]F (0.6-5 [deg]C)).
Droughts are not uncommon in Texas (Texas Water Resources Institute
2011, pp. 1-13). The most severe drought recorded in Texas occurred in
the 1950s, and in the last 15 years there have been widespread
droughts: in 1996, 1999-2000, 2005-2006, 2007, and 2010-2011 (Texas
Water Resources Institute 2011, pp. 10-12). Projections are for winter
precipitation to decrease by 5 to 30 percent, although it may increase
by 10 percent in other seasons (Environmental Protection Agency 1997,
p. 2).
East Texas is subtropical with a wide range of extremes in weather
(Diggs et al 2006, p. 65). Mean annual temperatures range from 70
[deg]F (21 [deg]C) in the south to approximately 64 [deg]F (18 [deg]C)
in the north, although extremes like 0 [deg]F (-18 [deg]C) and 110
[deg]F (43 [deg]C) are observed occasionally. The highest reported
eastern Texas temperature was 118 [deg]F (48 [deg]C) in Collin County
in 1936 (Bomar 1995, in Diggs et al. 2006, p. 65). Average rainfall
ranges from 60 in (152 cm) at the State's southeastern border to 40 in
(98 cm) at the western edge. These rainfall differences are related to
proximity to the warm, moist air supplied by the Gulf of Mexico. The
native vegetation of this region evolved with, and is adapted to,
recurrent extremes (Diggs et al. 2006, p. 67). That said, the
Pineywoods region is vulnerable to even small climatic shifts because
it is ``balanced'' on the eastern edge of a dramatic precipitation
gradient. Temperature increases that are projected in climate change
scenarios will likely be associated with increases in transpiration and
more frequent summer droughts. Decreased rainfall may result in an
eastward shift in the forest boundary and replacement of the Pineywoods
forest with scrubland (Diggs et al. 2006, p. 80). There is potential
for loss of species that are limited to mesic conditions of deep east
Texas, such as the hardwood forests surrounding the Weches glades.
There may also be a northerly shift of southerly species based on
climate models that predict increasing temperatures and, therefore,
increasing evapotranspiration and decreasing regional precipitation and
soil moisture (Diggs et al. 2006, p. 73).
Although east Texas has typically received a greater amount of
precipitation during December through March than other regions
(Neilsen-Gammon, p. 24), future precipitation trends indicate a
decrease in precipitation toward the middle of the 21st century
(Nielsen-Gammon, p. 28). The timing of this precipitation is crucial
for the Texas golden gladecress, which is dependent on late-fall-
through-spring moisture to generate the seeps and pooling that it
requires for germination, growth, and reproduction. Reproduction is
known to be negatively impacted by drought as evidenced by declines of
91 to 67 plants at the Chapel Hill site and 490 to 96 plants at the
Caney Creek Glade Site 1 during the 1999-2000 droughts (Service 2010b,
p. 5; Singhurst 2011a, pers. comm.). It is unknown how the Texas golden
gladecress will respond to continued years of drought, especially when
combined with other threats. Godwin (2012, pers. comm., p. 4) noted
that droughts have had a major effect on the distribution of biota in
east Texas and hypothesized that drought has contributed to isolation
and endemism in the glade flora.
A warmer climate with more frequent droughts, but also extreme
precipitation events, may adversely affect Texas golden gladecress by
altering the glade habitat the species is known to occupy. It may
improve habitat conditions for invasive plant species and other plants
(Service 2010b, p. 5), although, conversely, extreme drought years may
contribute to keeping woody species from overtaking glades by making
the shallow soil even more inhospitable to larger plants. Godwin (2012,
pers. comm., p. 1) personally observed the drought of 2011 ``pushing
back'' the edges of Weches glades and tiny saline prairies. Climate
extremes, especially drought and low temperatures, probably play a
bigger role in excluding nonadapted species than average conditions
will (Diggs et al. 2006, p. 80). Because the Texas golden gladecress is
a habitat specialist, being closely tied to the geology and soils on
the Weches outcrops, it seems unlikely that this species will be
flexible in terms of shifting to new habitats if the glades become
unsuitable due to lack of winter-spring moisture. Also, if conditions
shift in favor of nonnative plants, the Texas golden gladecress will
likely be negatively affected. Although the Texas golden gladecress has
survived cycles of drought in the past, as well as some years with
extraordinary temperature shifts, it may have done so in a landscape
where it was more abundant and with populations distributed in closer
proximity to one another. Based on our review, the best scientific and
commercial data available did not provide us with information regarding
the species' seedbank, so we do not know how many consecutive years of
poor conditions (in terms of low rainfall and high temperatures) the
species can survive.
The best scientific and commercial data available do not provide
reliable predictions for future patterns of precipitation and
temperature that are specific to east Texas. While it appears
reasonable to assume that climate change will occur within the range of
Texas golden gladecress, at this time we do not have information to
indicate specifically how climate change may affect the species, its
habitat, or responses of invasive species in these habitats.
Other Conservation Efforts
Habitat conditions conducive to the Texas golden gladecress's
persistence are being maintained at the Chapel Hill population site by
the landowner. Texas golden gladecress was an incidental
[[Page 56054]]
beneficiary of a brush removal project done for white bladderpod at
this site in 1995, when the private landowner, working in cooperation
with the Service, cleared shrubby overgrowth from his small tract of
land. As a result of this glade being reopened, the Texas golden
gladecress reappeared after a 10-year absence (Nemec 1996, p. 5). This
success demonstrated that removal of woody and weedy invaders may help
the Texas golden gladecress seedbed to germinate and the plant to
emerge. Because this site experienced rapid reinvasion of shrubs,
repeated maintenance was required to keep the site open, and the
landowner has voluntarily continued to mow or bushhog at least once per
year (Singhurst 2012f, pers. comm.). As a result, the Texas golden
gladecress and bladderpod were still seen to occupy this site as
recently as February 2012 (Singhurst 2012f, pers. comm.).
Within the past several years, the Service's Partners for Fish and
Wildlife Program has funded a habitat restoration project involving
brush clearing and planting of white bladderpod in a glade at a
privately owned tract in San Augustine County. It was also hoped that
Texas golden gladecress would benefit from this project, but the
species has not been detected at the site to date.
A past conservation effort proved that there is some potential to
reintroduce or create new populations of Texas golden gladecress. The
species was successfully introduced via seed into apparently
appropriate habitat in Nacogdoches County at a site located
approximately 30 mi (48 km) west of its historic range in the late
1980s, where it continued to grow until 2011, when a pipeline
excavation eliminated the population. The success of this introduction
effort was a positive indication of possibilities to augment existing
population sites or introduce Texas golden gladecress into other
currently unoccupied but suitable habitat sites to form new
populations.
In addition to habitat projects, the Service funded several
projects with TNC, including one that provided for 3 years of status
surveys for Texas golden gladecress and white bladderpod. These
surveys, completed in 2006, were the sole source of population numbers
for these species for several years. TNC also attempted to identify
appropriate glade habitats in which Texas golden gladecress and white
bladderpod might be found using GIS data (aerial, geology, and
hydrology sources) (Turner 2000 pers. comm.), but follow-up site visits
showed little Weches habitat and no new Texas golden gladecress
populations at what appeared to be suitable sites (Turner 2003, p. 4,
in Service 2010a). In 2001, TNC collected Texas golden gladecress seeds
from four sites for cultivation, research, and long-term storage, and
as seed sources for reintroduction work. The seeds were given to Mercer
Arboretum, where they have been in long-term storage, as well as being
used for some early germination and cultivation work. The species was
successfully introduced into apparently appropriate habitat in
Nacogdoches County at a site located approximately 30 mi (48 km) west
of its historic range in the late 1980s, where it grew and reproduced
through 2011, when it was eradicated by construction of a pipeline. The
success of this reintroduction project may bode well for future efforts
to increase the numbers of populations by reintroductions or
introductions to new sites.
Summary of Factor A
The threat that has the most significant impacts to Texas golden
gladecres populations is the loss and degradation of habitat.
Specifically, surface quarrying of glauconite and the exploration and
development of oil and natural gas wells and associated roads and
pipelines have destroyed 50 percent of the known populations between
the mid-1990s and 2011. The threats from quarry development are likely
to continue, as glauconite is currently in demand for road bed and well
pad construction, as well as for use in fertilizer and as an animal
feed additive. For the past several years, energy exploration and
production, especially natural gas, has been active due to development
of the natural-gas-bearing Haynesville Shale, which underlies the
entire range of Texas golden gladecress. For the four remaining
populations, these activities pose ongoing threats because we cannot
predict whether new pipelines, well pads, roads, or quarries are
planned for the areas where the populations occur. The populations of
Texas golden gladecress are found mainly on privately owned land where
no level of protection for the plants is guaranteed. Portions of two
extant populations extend into SH ROWs where TXDOT has the ability to
provide some protections but only for those few plants that are on the
ROW. Much of the species' potential habitat throughout its range occurs
on private lands that have not been surveyed; therefore, the current
level of threats across these lands cannot be assessed. The excavation
activities associated with surface quarrying of glauconite and oil and
gas development are threats that have significant impacts to the known
extant populations and associated habitats of the gladecress, both now
and in the future.
We have also determined that the damage to Texas golden gladecress
plants and outcrop habitat that is associated with excavations may
occur when pipelines for water, sewer lines, gas connections to homes,
and communication lines are installed. New power lines that are built
outside of established ROWs also have potential to damage Texas golden
gladecress populations and habitat if land-clearing activity and heavy
equipment directly cross occupied outcrops. Although we acknowledge
that these activities constitute potential threats to the species and
its habitat, we do not know where service improvements are planned
within the range of the species or the number of these types of
projects that are planned for the future.
Texas golden gladecress also faces threats throughout its range
from competition for light and nutrients from both native and
nonnative, invasive, woody plants, including the nonnative Macartney
rose. We have determined that the extant populations will decline or
become extirpated unless they are periodically maintained to remove
invading trees and shrubs. Additionally, herbicides used to control
Macartney rose may be a threat to the Texas golden gladecress if
applied to or persisting in the soil during the species' period of
growth, from late fall through early summer.
A recent, ongoing trend in local land use is the conversion of open
pasture to pine plantations. However, densely planted pine trees may
degrade the species' habitat due to competition for light and nutrients
and by contributing masses of leaf litter onto formerly sparsely
vegetated glades.
Finally, the information regarding climate change is not yet
specific enough for us to determine the potential long-term effects to
the Texas golden gladecress's habitat. However, long-term drought has
negatively affected and will likely continue to negatively affect the
reproduction and germination of Texas golden gladecress seeds.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Limited collection of Texas golden gladecress has occurred for
scientific purposes; only voucher specimens and several seed collection
events are documented. Dr. Elray Nixon collected seed in 1987, and
successfully created a new population when he introduced the seed onto
an outcrop in Nacogdoches County. TNC collected seed at four sites in
2001, and contributed these seed
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collections to Mercer Arboretum, a participating institution in the
Center for Plant Conservation, in 2002 (Tiller 2013, pers. comm., p.
1). Mercer maintained some in long-term storage and planted some in
germination trials. There are no records of any collections of seeds or
other plant materials in the last few years. Because these collections
were limited, we do not believe that this activity constitutes a threat
to the species. There is no information to suggest that Texas golden
gladecress is collected for commercial, recreational, or educational
purposes, and we have no reason to believe that this factor will become
a threat to the species in the future. Therefore, based on our review
of the best available scientific and commercial information, we
conclude that collection or overutilization of Texas golden gladecress
is not currently a threat to the species, nor do we expect it to become
a threat in the future.
C. Disease or Predation
Our review of the best available scientific and commercial
information regarding disease in Texas golden gladecress does not
indicate that disease or predation are issues for this species. There
is no information regarding predation by wildlife on the species.
Grazing is ongoing across the range of the Texas golden gladecress and
occurs on portions of all extant population sites; however, there is no
information to document that cattle eat Texas golden gladecress. No
studies have been conducted to investigate the effect of grazing or
herbivory specifically on Texas golden gladecress. George (1987, p. 17)
studied the herbaceous flora of three Weches outcrops in San Augustine
County and saw little grazing within his study plots although cattle
were present at all three sites. Therefore, based on our review of the
best available scientific and commercial information, we conclude that
disease and predation on Texas golden gladecress, including predation
associated with grazing, are not currently threats to the species, nor
do we expect disease or predation to become a threat in the future.
D. The Inadequacy of Existing Regulatory Mechanisms
Under this factor, we examine whether existing regulatory
mechanisms are inadequate to address the threats to the species
discussed under the other factors. Section 4(b)(1)(A) of the Act
requires the Service to take into account ``those efforts, if any,
being made by any State or foreign nation, or any political subdivision
of a State or foreign nation, to protect such species. . .''. In
relation to Factor D under the Act, we interpret this language to
require the Service to consider relevant Federal, State, and tribal
laws, regulations, and other such mechanisms that may minimize any of
the threats we describe in threat analyses under the other four
factors, or otherwise enhance conservation of the species. We give
strongest weight to statutes and their implementing regulations and to
management direction that stems from those laws and regulations. An
example would be State governmental actions enforced under a State
statute or constitution, or Federal action under statute.
Having evaluated the significance of the threat as mitigated by any
such conservation efforts, we analyze under Factor D the extent to
which existing regulatory mechanisms are inadequate to address the
specific threats to the species. Regulatory mechanisms, if they exist,
may reduce or eliminate the impacts from one or more identified
threats. In this section, we review existing State and Federal
regulatory mechanisms to determine whether they effectively reduce or
remove threats to the Texas golden gladecress.
The greatest threats to the Texas golden gladecress include loss of
habitat and the plants themselves due to actions that remove the
substrate under the populations or that cover them up. These types of
actions have been associated with quarrying of glauconite; construction
related to natural gas and oil exploration and production; conversion
of native glades or pastures with glades and outcrops to other land
uses, most recently planting to pine plantations; installation of
service lines; and potentially herbicide applications for purposes of
controlling the invasive Macartney rose.
Existing State and Federal regulations that might help conserve
rare species on SH ROWs, including avoidance or minimization of habitat
destruction, as well as regulations that would protect plants from
herbicide applications, are requirements only for already listed
species; therefore, these regulations do not apply to Texas golden
gladecress. Of the two Texas golden gladecress populations that occur
in ROWs, the federally listed white bladderpod is only found at one
site (Caney Creek Glade Site 1). Although the Texas golden gladecress
plants at the Caney Creek Glade Site 1 do extend into the TXDOT-
maintained ROW, the majority of the plants are on the adjacent private
land, so any protections offered by the State would apply to very few
of the plants. Likewise, no existing regulations protect the species on
privately owned land, where most of the remnant Texas golden gladecress
is found.
Currently, Texas golden gladecress is not protected by State or
Federal laws. All of the populations occur on private property even
though portions of those populations extend onto SH ROWs; the ROW
portions of these populations are miniscule. As such, the existing
regulatory mechanisms are inadequate to address the threats to the
species.
E. Other Natural or Manmade Factors Affecting Its Continued Existence
Small Population Size
The Texas golden gladecress remains in only three small
populations. Small populations can be prone to extirpation, especially
if a series of drought years greatly reduces seed production and
depletes the soil seed bank. The Service (1992, p. 8) noted that for a
species like the white bladderpod, with only small populations and wide
natural annual fluctuations in plant numbers, as well as fragmented
habitat across its range, recolonization after a population loss would
require long-distance seed dispersal. Although we have no information
regarding the Texas golden gladecress's seed dispersal patterns or
distances, we do know that the Texas golden gladecress's habitat is
exceedingly fragmented, with fewer and smaller known populations than
the bladderpod, and farther distances between populations. This makes
the prospects for recolonization after a potential loss of a Texas
golden gladecress population very remote.
Small populations can also be prone to extirpation from a single
adverse natural or manmade event. The population at the Chapel Hill
site is a good example of this vulnerability. Carr (2005, p. 2)
reported that Texas golden gladecress habitat was extremely limited at
Chapel Hill and that the numbers of Texas golden gladecress plants
would also always be restricted by the small size of the available
habitat. He concluded that the population was so small that a single
adverse event could extirpate the species from this location. The small
population size and the small number of extant populations of Texas
golden gladecress increases each population's vulnerability to the
threats that have significant impacts described under Factor A. Low
numbers of plants, confined to very small areas, can be totally
eradicated by actions such as installation of pipelines; excavation of
mines; or construction of well pads, roads, or other types of
construction. The remaining Texas golden gladecress occurrences are so
small that they can fall completely within the footprint of one well
pad, or even within the width of a pipeline excavation. Small
[[Page 56056]]
population size also increases the risk of total loss of populations
due to contact with herbicides or shading and leaf litter accumulation
from pine tree plantings because these threats are likely to affect the
entirety of any given occurrence. Sustained drought may reduce the
reproductive effort of a population, and this can lead to an overall
decrease in fitness for the remaining populations. Reduced reproductive
effort affects the seed bank, which represents the reproductive
capacity of each Texas golden gladecress population. The combined
effects of drought, impacts from oil and gas development, herbicide
treatment, shading, and competition place the remaining three
populations at a high risk of extinction, exacerbated by their small
population size and narrow distribution.
In addition to increasing vulnerability to direct threats such as
pipeline construction, small population size can result in a decrease
in genetic diversity due to genetic drift (the random change in genetic
variation in each generation) and inbreeding (mating of related
individuals) (Antonovics 1976, p. 238; Ellstram and Elam 1993, pp. 218-
219). Genetic drift can decrease genetic variation within a population
by favoring certain characteristics and, thereby, increasing
differences between populations (Ellstram and Elam 1993, pp. 218-219).
This increased difference between populations can diminish a species'
ability to adapt to the selective pressures of a changing environment
(Newman and Pilson 1997, p. 360; Ellstrand 1992, p. 77). Self-
fertilization and low dispersal rates can cause low genetic diversity
due to inbreeding (Antonovics 1976, p. 238; Barrett and Kohn 1991, p.
21).
Although we do know that Texas golden gladecress exists in small
populations in a fragmented landscape, we do not know whether these
remaining populations are peripheral to what may have been a
historically larger range. Although we might infer inbreeding is
occurring in gladecress based on the species' isolated occurrences and
ability to self-fertilize, the best scientific and commercial data
available do not describe genetic diversity exhibited by the species.
Summary of Factor E
Texas golden gladecress is a historically rare species with some
adaptations, such as a mixed mating system, that help to alleviate part
of the inherent risks of small population size. The continued existence
of Texas golden gladecress is negatively impacted by natural factors
including being limited to only a few remaining populations that
contain very small numbers of individual plants with a distribution
restricted to extremely small areas of outcrop. The species' current,
reduced occurrences across a range that has been highly fragmented by
past and ongoing human activities increase its vulnerability. With only
three remaining populations, loss of an entire population could be
catastrophic for this species' long-term viability. Therefore, based on
our review of the best available scientific and commercial information,
we conclude that the small number of remaining populations, all of
which are small in size, in conjunction with the threats described
under Factor A, constitutes a threat to the species and greatly
exacerbates other the threats we identify above for this species.
Conservation Efforts To Reduce Other Natural or Manmade Factors
Affecting Its Continued Existence
We have several examples of voluntary conservation efforts that are
currently underway, or which took place in the past, that directly, or
indirectly, assist the Texas golden gladecress by addressing the
impacts of habitat loss and degradation, or low population and
individual plant numbers. See description under the Factor A analysis,
above.
Cumulative Effects From Factors A Through E
As described above under Factor E, Texas golden gladecress's small
population size and the small number of extant populations increase
each population's vulnerability to the significant threats described
under Factor A. Small numbers of plants, confined to very small areas,
can be extirpated by actions such as installation of pipelines;
excavation of mines; or construction of well pads, roads, or other
types of construction. The remaining Texas golden gladecress
populations are so small that they can fall completely within the
footprint of one well pad, or even within the width of a pipeline
excavation. This has been the case for four of the eight Texas golden
gladecress populations ever documented; three of these were extirpated
due to quarry excavation between the late 1980s and the mid-1990s. The
continued threat of extirpation of populations to excavation projects
continues, as evidenced by the loss of the fourth population (the
introduced population) to a pipeline installation as recently as 2011.
Small population size also increases the risk of total loss of
populations due to contact with herbicides or shading and leaf litter
accumulation from pine tree plantings because these threats are likely
to affect the entirety of any given occurrence. The high incidence of
Macartney rose invasion within the Texas golden gladecress's range
could increase the species' likelihood of exposure to herbicides
associated with Macartney rose-control projects.
The overgrowth of many glade habitats by woody shrubs, particularly
Macartney rose and Chinese privet, within the range of Texas golden
gladecress also puts these few small populations at an increased risk
of genetic isolation if the plant is forced into dormancy by hostile
conditions on the glade. Sustained drought could also reduce the
reproductive effort of a population, and this can lead to an overall
decrease in fitness for the remaining populations. Reduced reproductive
effort affects the seed bank, which represents the reproductive
capacity of each Texas golden gladecress population.
The combined effects of drought, impacts from oil and gas
development or other excavations, herbicide treatment, shading, and
competition place the remaining three populations at a high extinction
risk, and this is exacerbated by their small population size and very
restricted geographic distribution.
Determination
Standard for Review
Section 4 of the Act, and its implementing regulations at 50 CFR
part 424, set forth the procedures for adding species to the Federal
Lists of Endangered and Threatened Wildlife and Plants. Under section
4(b)(1)(A), the Secretary is to make endangered or threatened
determinations required by subsection 4(a)(1) solely on the basis of
the best scientific and commercial data available to her after
conducting a review of the status of the species and after taking into
account conservation efforts by States or foreign nations. The
standards for determining whether a species is endangered or threatened
are provided in section 3 of the Act. An endangered species is any
species that is ``in danger of extinction throughout all or a
significant portion of its range.'' A threatened species is any species
that is ``likely to become an endangered species within the foreseeable
future throughout all or a significant portion of its range.'' Per
section 4(a)(1) of the Act, in reviewing the status of the species to
determine if it meets the definition of endangered or threatened, we
determine whether any species is an endangered species or a threatened
species because
[[Page 56057]]
of any of the following five factors: (A) The present or threatened
destruction, modification, or curtailment of its habitat or range; (B)
overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; and (E) other natural or manmade
factors affecting its continued existence.
Listing Status Determination
Based on our review of the best available scientific and commercial
data, we conclude that the Texas golden gladecress is currently in
danger of extinction throughout all of its range and, therefore, meets
the definition of an endangered species. This finding, explained below,
is based on our conclusions that the severity of threats is high and
occurs throughout the range of the species. The Texas golden gladecress
has demonstrated some ability to survive certain events (dozing and
drought) likely due to persistent seed bank and some ability to
tolerate small population sizes likely due to self-fertilization.
However, it shows little to no ability to survive or tolerate other
impacts (quarry mining and pipelines). Further, although somewhat able
to persist in the face of past naturally occurring stochastic events,
the species is currently highly vulnerable due to the limited
distribution of populations across its range and to the specific
habitat requirements needed to support the species. We find that the
Texas golden gladecress is at an elevated risk of extinction now, and
there is no information to suggest that the species' status will
improve without significant conservation intervention. We, therefore,
find that the Texas golden gladecress meets the definition of an
endangered species under the Act.
On the basis of our biological review documented in this final rule
to list the Texas golden gladecress, we find the species is vulnerable
to population extirpations due to its specialized habitat requirements;
restricted geographic distribution; moisture regime requirements;
small, isolated populations; and few remaining populations (Factors A
and E). The species is endemic to Weches glade habitat, which is
scattered or patchy across the landscape. Its historic range does not
extend farther than approximately 12 miles (19 km) from the most
southeastern to the most northwestern documented locations, and all
occurrences were located within a 3.1-mile-wide (5-km-wide) band around
SH 21. The extant populations exhibit a high degree of isolation, being
separated from each other by distances of 4.5 mi (7.2 km) and 7 mi
(11.3 km), respectively, between the northern (Caney Creek Glade Site
1), central (Chapel Hill), and southern (Geneva) populations. All three
extant populations are small in terms of areal extent and number of
individual plants. The remaining three sites cover less than 1.2 ac
(0.5 ha). The loss of any of the known populations further reduces the
ability of the species as a whole to withstand additional threats.
The remaining small, isolated Texas golden gladecress populations
are particularly susceptible to extirpation from habitat loss and
degradation (Factor A). The main sources of habitat loss and
degradation include construction of glauconite mines, construction of
pipelines, and invasive woody plants. Glauconite mines and pipelines
remove the habitat and the overlying Texas golden gladecress plants,
which eliminates the entire glade or alters hydrology of glades nearby;
allow the invasion of the open, sunny glade habitats by native and
nonnative woody and weedy species; and can prompt the planting of pine
trees in close proximity to occupied glades, which reduces sunlight and
increases leaf litter. Drought decreases seed production. Successive
years of drought could lead to further declines in the numbers of
plants, or perhaps total loss of Texas golden gladecress populations,
if no growth or reproduction occurs over this extended time period, a
circumstance that could be exacerbated by climate change.
In addition to the individual sources of habitat loss and
degradation under Factor A, and small, isolated populations under
Factor E, the cumulative effects of the multiple stressors are acting
on populations such that the effects on the Texas golden gladecress, as
well as the immediacy of these threats, are significant throughout the
species' entire current range. The small and limited number of
remaining populations act in concert with the threats under Factor A
and E. These factors pose imminent threats to the species because they
are ongoing. The current conditions of small and isolated populations
reduce the ability of any given Texas golden gladecress population to
endure such adverse events, and natural recolonization following local
extirpations is considered unlikely in most cases.
We evaluated whether the Texas golden gladecress is in danger of
extinction now (i.e., an endangered species) or is likely to become in
danger of extinction in the foreseeable future (i.e., a threatened
species). The foreseeable future refers to the extent to which the
Secretary of the Interior can reasonably rely on predictions about the
future in making determinations about the future conservation status of
the species. A key statutory difference between an endangered species
and a threatened species is the timing of when a species may be in
danger of extinction either now (endangered species) or in the
foreseeable future (threatened species).
Because of the fact-specific nature of listing determinations,
there is no single metric for determining if a species is ``in danger
of extinction'' now. In the case of the Texas golden gladecress, the
best available information indicates that, while a major range
reduction (that is the overall geographic extent of the species'
occurrences) has not happened, habitat destruction has resulted in
significant loss of populations and reductions in total numbers of
individuals. These losses are ongoing, as at least one population was
lost due to a pipeline installation within the last 3 years and three
populations were lost between 1994 and 2011 due to quarry mining.
Because the types of human activities that have contributed to the
losses of Texas golden gladecress populations are continuing to occur
across the species' range, we anticipate that future losses of the
remaining populations are likely to occur. Additionally, degradation of
the species' habitat across its entire range is continuing as woody and
weedy plants overrun glade sites. Further, an increase in the number
and duration of drought events is projected to continue. Without
substantial conservation efforts, this trend of population loss is
expected to continue and result in an elevated risk of extinction of
the species. The narrow endemism of the species, with its small
geographic range, increases the risk for the species that stochastic
events (e.g., drought) will affect all known extant populations,
putting the Texas golden gladecress at a high risk of extinction.
Under the Act and our implementing regulations, a species may
warrant listing if it is endangered or threatened throughout all or a
significant portion of its range. The threats to the survival of this
species occur throughout its range and are not restricted to any
particular significant portion of its range. Accordingly, our
assessments and determinations apply to this species throughout its
entire range.
In conclusion, as described above, the Texas golden gladecress has
experienced significant reductions in population numbers (based on
habitat loss and degradation). The Texas golden gladecress is
especially vulnerable to impacts due to its life history and
[[Page 56058]]
ecology. The species is also subject to significant current and ongoing
threats. After a review of the best available scientific information as
it relates to the status of the species and the five listing factors,
we find the Texas golden gladecress is in danger of extinction now.
Therefore, on the basis of the best available scientific and commercial
information, we are listing the Texas golden gladecress as an
endangered species, in accordance with section 3(6) of the Act. We find
that a threatened species status is not appropriate for the Texas
golden gladecress because the threats to the species are occurring now
and are expected to continue into the future such that overall risk of
extinction is high at this time.
Neches River Rose-mallow
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Neches River rose-mallow is a nonwoody, flowering perennial found
within seasonally or regularly inundated sloughs, oxbows, terraces,
sand bars, and bottomlands. The Neches River rose-mallow is endemic to
relatively open habitat with hydric alluvial soils (water-saturated
soils). Sites are found within the Neches, Sabine, and Angelina River
basins and the Mud and Tantabogue Creek basins of five counties within
east Texas.
Nonnative Species
Nonnative plant species are a constant threat to native flora
throughout the Gulf coast prairies of Texas and Louisiana (McCormick
2005, p. 23). A primary threat to the Neches River rose-mallow is the
ongoing encroachment of nonnative and native woody species into its
generally open, intermittent or perennial wetlands. We considered the
potential threat from three nonnative species, Chinese tallow, coastal
bermudagrass, and bahiagrass (Miller 2011, pers. comm.). Based on the
best scientific and commercial data available, the Chinese tallow is an
ongoing threat to the Neches River rose-mallow, but coastal
bermudagrass and bahiagrass are not threats at this time.
Chinese tallow was introduced to the United States in the 1700s
from China (McCormick 2005, pp. 7, 8). With the ability to reproduce
quickly, reach reproductive maturity in as little as 3 years, and
remain reproductively mature for at least 60 years (United States
Geological Survey (USGS), 2000, p. 2) to 100 years (Gan et al. 2009, p.
1346), Chinese tallow can produce an abundance of seed annually (Potts
1946, p. 375; Conway et al. 2000, pp. 268-269). Chinese tallow
tolerates a range of habitat conditions, including full sunlight and
shade, and both flooding and drought-stricken habitats (USGS 2000, p.
1). These features allow Chinese tallow to dominate certain habitats.
Butterfield et al. (2004, p. 338) also found that Chinese tallow grew
faster than native species found within the Neches River rose-mallow
habitat, such as loblolly pine, water tupelo (Nyssa aquatica), blackgum
(N. sylvatica), and sweetgum, which occur in both perennially and
intermittently wet habitats. Without management, the Chinese tallow has
the ability to shade out, out-grow, and limit water and nutrient
absorption to Neches River rose-mallow and its native vegetative
associated species.
While there are methods to control Chinese tallow, these methods
are labor intensive, expensive, and limited in their effectiveness.
Burning, mechanical, and chemical (herbicide) means can be used to
control Chinese tallow; however, prescribed fire has produced complex
and highly variable results in Chinese tallow and may not be an
effective management tool (Grace 1998, entire; Grace 2011, pers.
comm.). The Davy Crockett NF is establishing a regular burn cycle of 3-
4 years for all compartments containing the Neches River rose-mallow to
control Chinese tallow and to mimic the historical fire regimes of the
Coastal Plain (Landers et al. 1990, p. 136). The Davy Crockett NF
Revised Land and Resource Management Plan for National Forests and
Grasslands in Texas (specific to the streamside Management Area 4 where
the Neches rose-mallow occurs) allows for mechanical means and
prescribed fire to maintain the native plant community but prohibits
the use of chemical agents (herbicides) unless applied by hand or
through nonaqueous form within 100 feet (30.5 m) of the Neches River
rose-mallow (United States Department of Agriculture 1996, p. 154).
Despite the available management actions, Chinese tallow remains at all
USFS sites. Current mowing activities along ROWs may abate some growth
of Chinese tallow, but management actions on these sites should also be
evaluated for their effectiveness. Chemical methods are not being used
to control Chinese tallow.
The invasion from nonnative Chinese tallow tree has historically
been a threat to the Neches River rose-mallow and continues to be a
threat. Chinese tallow occurs at all Neches River rose-mallow sites
(Miller 2011, pers. comm.) at varying densities and was found to be
most prevalent at SH 94 and compartment 16, Davy Crockett NF,
respectively (Walker 2012, p. 2). Without active or effective
management, Chinese tallow can reproduce quickly, out-shading Neches
River rose-mallow and other native woody vegetation and limiting its
water and nutrient absorption. Only select sites are being actively
managed for Chinese tallow, but the species has not been successfully
eradicated at any of the sites. This threat has led to declines at all
Neches River rose-mallow sites. Therefore, based on the best scientific
and commercial data available on this invasive, we conclude that
invasion from Chinese tallow is a threat across the species' range.
Coastal bermudagrass is not typically found within the wetland
habitats that the Neches River rose-mallow prefers, but three sites
have persisting stands of coastal bermudagrass: The Texas Land
Conservancy site, SH 204 ROW (Walker 2012, pers. comm.), and SH 94 or
Boggy Slough (Allen 2011a, pers. comm.). Site visits to east Texas that
included these three sites in August 2012, did not exhibit reduced
numbers of Neches River rose-mallow due to coastal bermudagrass.
Bahiagrass has not been found at any Neches River rose-mallow sites.
Coastal bermudagrass is an introduced bermudagrass cultivar that
has been widely planted in the southern United States for livestock
forage. It is adapted to a wide range of soil types and climates and
tolerates both drought and periodic inundation (Burton and Hanna 1985,
p. 247), much like the conditions of Neches River rose-mallow habitat.
In drier climates, this cultivar will thrive along irrigation ditches
and streambeds, agricultural fields, and roadside areas (Burton and
Hanna 1985, p. 247).
Due to its hybrid origin, coastal bermudagrass produces very few
viable seeds and is established by planting sprigs (rhizomes and
stolons) (Stichler and Bade 2012, p. 1); however once established,
coastal bermudagrass tends to produce dense monocultures where native
species cannot persist. A lack of management, including mowing, could
allow coastal bermudagrass to monopolize Neches River rose-mallow
habitats such that the bermudagrass would out-compete the rose-mallow
for water and nutrients and could out-shade the Neches River rose-
mallow. Along ROWs, coastal bermudagrass and bahiagrass are often
included in mixtures to re-seed ROWs in east Texas (Adams 2013c, pers.
comm.). The wetter, low-lying areas of the ROW where Neches River rose-
mallow exists are not generally planted with coastal bermudagrass.
TXDOT also mows along
[[Page 56059]]
ROWs, potentially diminishing any possible encroachment as coastal
bermudagrass and bahiagrass have not been observed to cause declines in
any Neches River rose-mallow population.
The threat from coastal bermudagrass and bahiagrass can have
potential impacts to native plants. However, only three sites have
coastal bermudagrass, and bahiagrass is not present at any of the
sites. It does not appear that Neches River rose-mallow has been
negatively impacted by either species as of yet or will likely be
impacted in the near future. Therefore, based on the best scientific
and commercial data available on coastal bermudagrass and bahiagrass,
and the lack of any observed impacts to the Neches River rose-mallow,
we conclude that they are not threats to the Neches River rose-mallow
across its range.
Native Species
Historical and current encroachment from native species has been
observed in Neches River rose-mallow habitat. Two species, sweetgum and
green ash (Fraxinus pennsylvanica), are native, deciduous trees of east
Texas that have been found at all Neches River rose-mallow sites
(Miller 2011, pers. comm.). Four Neches River rose-mallow populations
monitored in 2011 were overgrown with sweetgum and green ash (Miller
2011, pers. comm.; TXNDD 2012a, pp. 1-11, 20-28). About 36 percent (4
of the 11) of the Neches River rose-mallow's populations are impacted
by competition and shading from native sweetgum and green ash trees.
Sweetgum is found on a variety of soils but grows best on moist,
alluvial clay and sandy loams of river bottoms (Kormanik 2004, p. 790,
in Burns and Honkala 1990). Green ash also tolerates a range of soils
and in Texas is abundant in clay or silty loams of floodplains (Johnson
1980, in Gucker 2005, p. 15). Both species also grow in full sun to
partially shaded habitats. Therefore, both the sweetgum and green ash
are well adapted to the hydric alluvial soils and partial to open
canopies that the Neches River rose-mallow needs. In the absence of
other competing species, sweetgum and green ash can attain large sizes
(50-100 feet (15-30 m)) (Dickerson 2002, p. 1) and can reduce the open
canopy (Kirkman 1995, pp. 12, 15), thereby shading out Neches River
rose-mallow.
Historically, natural fires generally occurred every 1 to 3 years
in east Texas (Landers et al. 1990, p. 136; Landers 1991, p. 73) and
controlled both native and nonnative species. Naturally occurring
wildfires or prescribed fires can be used as management tools to limit
the abundance of these native tree species. Two of the four sites were
on ROWs, and prescribed burning is not a widely accepted method of ROW
maintenance. On the other two sites, prescribed burning had not been
implemented. The TXDOT mows these ROW sites, but mowing does not appear
to be an effective management tool because these sites have both
historic and current observations of native species encroachment.
Four of the 11 sites are impacted by native species, the current
management techniques are not adequate for control of native species,
and effective techniques need to be investigated. Therefore, based on
the best scientific and commercial data available, the effects of
native encroachment by these species pose an ongoing threat to the
Neches River rose-mallow.
Hydrological Changes
Habitat where Neches River rose-mallow is found includes both
intermittent and perennial wetlands along oxbows, sloughs, terraces,
sand bars, and other low-lying areas in habitats with minimal standing
water. Wetlands are ecological communities with hydric (flooded or
saturated) soils. Many wetland species, including the Neches River
rose-mallow, are adapted to highly variable rates of water flow,
including seasonal high and low flows, and occasional floods and
droughts. For example, the Neches River rose-mallow likely requires
high precipitation and flowing water or flood events to disperse seed
(Warnock 1995, p. 20; Scott 1997, p. 8; Reeves 2008, p. 3), and
although the Neches River rose-mallow is adapted to persisting in dry
conditions during portions of the year, a complete lack of water can
diminish seed production, range expansion, and genetic exchange. As
Neches River rose-mallow habitat is so water-dependent, hydrological
changes can have huge impacts. Some degree of hydrological change has
been seen at most of the Neches River rose-mallow sites; however,
information on some of the private land sites is lacking.
At the Boggy Slough site, which is connected to the SH 94 site,
natural shifts of river and creek beds have left meandering scars and
remnant oxbows. However, several levees upstream and the creation of a
duck hunting pond on this site have changed the natural landscape and
flow patterns, thereby converting seasonally inundated wetlands to
permanently flooded wetlands (Miller 2011, pers. comm.). Beaver
activity, such as selective cutting and damage to certain tree species,
was evident at the Boggy Slough site, but the Neches River rose-mallow
did not show impacts.
On another private land site, The Texas Land Conservancy site
(referred to as the Lovelady site in Table 4, above), Neches River
rose-mallow plants were once observed lining the perimeter of a
flatwoods pond. However, after 2003, when a stock pond was constructed
(TXNDD 2012a, p. 18) in what was likely part of an overflow channel
from Tantabogue Creek, the natural surface hydrology was altered by
retaining overflow, preventing it from draining south to the site
containing Neches River rose-mallow plants. The Texas Land Conservancy
was considered a robust population; however, in 2011, the Service and
TPWD botanists only observed 539 Neches River rose-mallow stems, most
of which were in relatively poor condition (Miller 2011, pers. comm.).
All four Davy Crockett NF sites (compartments 55, 16, 11, and 20)
censused in 2011 were completely dry except for compartment 20, where a
small pond to the south drains into the compartment (Miller 2011, pers.
comm.). Compartment 16 had altered hydrological changes. In 2000, when
the Neches River rose-mallow was introduced into a wetland on this
compartment, a beaver dam was present. When the dam broke in 2002,
water infiltrated the site, and the original hydrology was altered
(TXNDD 2012a, p. 44). Plant numbers decreased from 450 to 43 plants. It
is unclear if this decrease in plants was due directly to the loss of
the beaver dam; this needs further research. The pine-oak forest on
adjacent private land west of compartment 55 helps regulate the amount,
timing, and possibly the rate of water flow into the compartment.
Therefore, any alteration of the pine forest, through tree removal
projects or other habitat-altering activities, could alter key
hydrological characteristics of this compartment. However, the
likelihood of tree removal projects or habitat alteration activities on
adjacent lands is unknown but likely minimal.
Water development and construction projects could also result in
the complete loss or inundation of water at sites, threatening the
Neches River rose-mallow. In 1978, the Angelina and Neches River
Authority (ANRA) proposed the construction of a reservoir known as Lake
Columbia (previously known as Eastex), in Cherokee and Smith Counties,
Texas (ANRA 2012), to supply water for five surrounding counties (U.S.
Army Corps of Engineers (USACE), 2010, pp. 2-4, 3-43). The dam for this
reservoir would be constructed on Mud Creek and would impound
[[Page 56060]]
approximately 195,500 acre-feet (ac-ft) (241 million cubic meters
(mcm)) of water in a reservoir reaching 14 mi (22.5 km) upstream (USACE
2010, p. 1-1). Up to 85,507 ac-ft (1,105 mcm) of water would be
diverted from the downstream flow of Mud Creek (USACE 2010, p. 1-1).
According to the most current project plans available in the draft
environmental impact statement (EIS), a habitat evaluation procedures
analysis (a broad habitat-based approach to assess environmental
impacts of proposed water and land resource development projects)
stated that it was possible for the Neches River rose-mallow to be in
the permit area, if habitat exists; however, the analysis did not
document any Neches River rose-mallow in the permitted project area
(Walker 2011, pers. comm.; USACE 2010, p. 4-154). The ``Permitted
Project Area'' includes the footprint of the normal conservation pool
of the reservoir below a certain elevation and the limits of
construction in the vicinity of the dam, or a total of approximately
10,655 acres. The ``Downstream Impacts Area'' was also analyzed in the
EIS. This area included the existing Mud Creek 100-year floodplain for
a distance of approximately 16 miles from below the dam site to the
confluence with the Angelina River (USACE 2010, p. 1-4). The extant
Neches River rose-mallow population found at the intersection of SH 204
ROW and Mud Creek is within the downstream portion of the project that
was analyzed. The SH 204 ROW site is a perennial wetland where plants
generally remain inundated year round; therefore, a change in the water
level at this site could make it unsuitable for Neches River rose-
mallow or could restrict potential seed dispersal mechanisms. Drought
conditions could also exacerbate the potential threats from this
project, and the reduced downstream water flows could completely
extirpate the SH 204 ROW site (USACE 2010, p. 4-154; Heger 2012, pers.
comm.).
Using the best scientific and commercial data available, we
anticipate that the construction of the Lake Columbia reservoir project
will divert water downstream, thereby likely dewatering the SH 204 ROW
site. The agencies involved with the project are still working on
solidifying the project details, and, therefore, we do not know how
much water will remain at this site or if future water management
practices or decisions will allow for seasonal flooding of water to
this site.
Optimal habitat conditions for Neches River rose-mallow include
intermittent or perennial wetlands that can be variable throughout the
year, often becoming surficially dry during the summer and wet during
the winter, perhaps being exposed to water year-round. However,
hydrological changes that result in the complete loss or inundation of
water at the site threaten the Neches River rose-mallow. Neches River
rose-mallow, despite its name, is not found in deeper waters, unlike
other Hibiscus species, and the Neches River rose-mallow is thought to
need water at some point of its life cycle for seed dispersal. A
complete loss of water at any or all of the sites could restrict the
exchange of genetic material between and among sites, thereby
compromising the species' genetic integrity.
Although the severity of impacts from beaver dams to the Neches
River rose-mallow could be high, the level of exposure to this stressor
is low. Consequently, we do not consider beaver dams a threat at this
time. However, the severity of altered hydrology as a whole is high and
the exposure of this threat is present throughout the species' range.
Consequently, we have determined that altered hydrology is a threat now
and will continue to be a threat in the near-future.
Upgrades and Construction for ROWs, Roads, Bridges, and Other
Structures
Right-of-way populations are vulnerable to bridge and road
expansion, new road construction, and upgrade projects. These
activities could impact the sites' hydrology, soil stability, wetland
and riparian vegetation, and water quality. Hydrological changes,
erosion, and changes in the associated native vegetation due to ROW and
road upgrades and construction projects are threats to the species (as
described in detail in the ``Nonnative Species,'' ``Native Species,''
and ``Hydrological Changes'' sections, above). We do not have
information on how sedimentation and changes in water quality could
impact Neches River rose-mallow; however, increased siltation within
the water column is the major pollutant of wetlands in the United
States (Baker 1992; USEPA 1995).
In 2005, a proposed bridge replacement on SH 230 ROW would have
altered approximately 4.91 ac (2 ha) of Neches River rose-mallow
habitat south of the ROW and 0.07 ac (0.03 ha) north of the ROW (Adams
2005, p. 1), but the TXDOT implemented avoidance measures. Bridge
replacement and road expansion projects are continuing along SH 94 ROW,
but as of 2011, had not progressed into Neches River rose-mallow
habitats (Adams 2011c, pers. comm.). For this project, TXDOT is using
temporary culverts and silt fencing to reduce sedimentation, and the
Neches River rose-mallow site has been fenced off to prevent access.
Regardless of these minimization techniques, sedimentation was evident
along SH 94 ROW (Walker 2012, p. 2).
Potential road projects are mainly restricted to ROW easements and
may potentially impact three of the 11 extant populations. Roadwork
along SH 230 is occurring, and based on communication with the TXDOT,
there will likely be only one project in road ROWs within the Neches
River rose-mallow sites. These activities are currently being
implemented or will be in the near future. As a result, the impacts to
Neches River rose-mallow could be high, as an entire population could
be removed as a result of these activities. Consequently, we conclude
that SH ROW maintenance, bridge maintenance, and other structural
projects are a threat to Neches River rose-mallow populations now and
will continue to be a threat into the future.
Silviculture
Pine plantations in east Texas are established mainly on uplands
that are managed to mimic old fields or grassy savannas (Fox et al.
2007, p. 340). Site preparation may include anchor chaining, chopping,
burning, root raking, shearing, and disking (Balmer and Little 1978, p.
60). One Neches River rose-mallow population on private property south
of SH 230 was extirpated when the site was converted to a pine
plantation sometime after 2003 (Poole 2011b, pers. comm.; TXNDD 2012a,
pp. 61-67). Three additional sites in or near Neches River rose-mallow
populations have shown evidence of habitat-clearing activities to
prepare land for harvesting trees, including: Adjacent land south of
the Davy Crockett NF compartment 55, Houston County; an extirpated site
located south of the extant Lovelady site, Houston County; and the
privately owned site at Champion, Trinity County.
Although silviculture impacts have occurred in the past, the
likelihood that silviculture activities (including land-clearing
activities and actual planting of trees) will occur in the near future
is very low on the occupied units, including the three ROW sites and on
the four USFS sites. In addition, the wetland habitat does not
necessarily exclude silviculture from occurring on sites, but wetlands
are not usually considered the best sites for pine planting. Therefore,
we conclude that silviculture activities are currently not a threat to
the Neches River rose-mallow.
[[Page 56061]]
Herbicide Use
Herbicide treatments are increasingly popular because they remove
unwanted plant growth without causing soil erosion from the site;
however, herbicide use increases incidents of water pollution and
aerial drift to nontarget sites (Balmer and Little 1978, p. 63). There
have been several instances where herbicide impacts to Neches River
rose-mallow plants on ROWs and on privately owned lands have been
documented. Neches River rose-mallow populations may also be
potentially impacted by herbicides applied to pine plantations that
drift into the Neches River rose-mallow habitat. Normal rainfall and
flood events can unintentionally disperse herbicides downstream,
impacting individual plants or whole populations, depending on the
nature of the herbicide.
Three subpopulations in Trinity County along SH 230 experienced
impacts from herbicide spraying. One subpopulation with approximately
50 plants, on private property south of SH 230, was extirpated by
herbicide use (Service 2010b, p. 7). Herbicide drift at a second
subpopulation along SH 230 (Gordon 2009, pp. 3-4) caused the ROW
population to decline from 14 plants in 1999 (Poole 2001, p. 2) to zero
plants in 2002 (Miller 2011, pers. comm.). Herbicide damage was evident
at a third subpopulation along SH 230 ROW, and could have been the
result of herbicide use by the private landowner south of SH 230 (what
is now planted in pine), but this has not been confirmed. In 2012, a
graduate student from Stephen F. Austin State University noted Neches
River rose-mallow at this site, but this needs to be confirmed.
The TXDOT used herbicides to remove woody vegetation from ROWs in
the past (Miller 2005, pers. comm., in Service 2006, p. 7; Adams 2011c,
pers. comm.), but mechanical clearing methods have largely replaced the
use of herbicides in these ROW areas. Impacts from herbicide
applications to Neches River rose-mallow have not been documented at
any of the four USFS compartments. The USFS Revised Land and Resource
Management Plan for National Forests and Grasslands in Texas restricts
the use of nonaquatic herbicides unless hand-applied (United States
Department of Agriculture 1996, p. 153).
Exposure to herbicides, in conjunction with silviculture
activities, is a threat to the Neches River rose-mallow, as it has
impacted seven of the 11 populations (64 percent). While the majority
of Neches River rose-mallow populations are on State or Federal land,
all are adjacent to private lands. Even though the State and the USFS
do not actively use herbicides, private landowners do. Consequently,
herbicide overspray from private land could impact all existing Neches
River rose-mallow populations. The severity of herbicide use effects to
the Neches River rose-mallow, in combination with silviculture
practices, is high, as seven of the 11 populations have been impacted
by these activities. These activities are current and ongoing threats.
Consequently, exposure to herbicides is a current and near future
threat to the Neches River rose-mallow.
Trampling and Herbivory by Feral Hogs and Cattle
Feral hogs (Sus scrofa) were first introduced to the mainland of
North America (Wood and Barrett 1979, pp. 237, 238) in Texas in 1542,
although large-scale introductions did not occur until the 1930s (Isle
and Hellgren 1995, p. 793). While these omnivores dig in the soil in
search of roots, tubers, and invertebrates, they can inadvertently
cause damage to other food resources and habitat. Feral hogs forage by
turning over soil with their snouts, creating mounds and depressions
(Arrington et al. 1999, p. 535). Hogs transition from foraging in oak
stands during winter months, to foraging in swamp and marsh edges
during the summer months to feed on grasses, sedges, tubers, and roots
(Wood and Roark 1980, pp. 507-509). Feral hogs are able to travel long
distances to feed, and often uproot vast areas of habitat. Feral hogs
reach sexual maturity at 6 to 8 months (Wood and Barrett 1979, p. 242),
and have large litter sizes. However, uprooting of Neches River rose-
mallow has not been observed (Creech 2011a, pers. comm.; Miller 2011,
pers. comm.).
There are both historic and current records of damage to Neches
River rose-mallow habitat from feral hogs. Damage of habitat by feral
hogs has historically been recorded at Mill Creek Gardens (Creech
2011a, pers. comm.; Miller 2011, pers. comm.) and on all four Davy
Crockett NF sites. Until 2012, only tracks and damage to habitat have
been the most noted type of destruction; however, current damage to
Neches River rose-mallow plants was observed in compartments 16 and 20
of the Davy Crockett NF, where feral hogs had broken and flattened
plants (Walker 2012, pers. comm.). Large groups of feral hogs were
observed in Neches River rose-mallow sites within compartments 55 and
16 of the Davy Crockett NF (Walker 2012, pers. comm.). Habitat damage
is rangewide, and although Neches River rose-mallow may not the primary
target during foraging activity, plants have been damaged.
Although the Neches River rose-mallow grows adjacent to permanent
standing water or may occur within infrequently flooded areas, this
does not limit the access of feral hogs. Further, drought may enhance
accessibility to Neches River rose-mallow sites, thus increasing their
susceptibility to trampling by feral hogs. Unmanaged feral hog
populations can lead to increased soil disturbance and impacts to the
native vegetative community, which could create prime conditions for
nonnative species to invade. Current feral hog damage has been
documented at four of the 11 Neches River rose-mallow sites. Feral hogs
are a present threat and will likely continue to be a threat in the
near future. However, at this time the severity of impacts to the
Neches River rose-mallow is low.
It is estimated that livestock grazing has damaged 80 percent of
stream and riparian ecosystems in the southern United States (Belsky et
al. 1999, p. 419). The damage includes increased sedimentation,
decreased water quality, and trampling and overgrazed stream banks
where succulent (high water content) forage exists (Armour et al. 1994,
p. 10; Fleischner 1994, p. 631; Belsky et al. 1999, p. 419). Trampling
causes soil compaction and damage to both above- and below-ground
vegetative plant structures and increases soil erosion (Warren et al.
1986, p. 491).
Livestock owned by a neighboring landowner were observed on The
Texas Land Conservancy's Lovelady site in 2011. The Neches River rose-
mallow at the Lovelady site suffered severe documented herbivory where
stems had been eaten almost to the ground (TXNDD 2012a). The Texas Land
Conservancy has attempted to exclude these livestock, and has proposed
constructing an exclusion fence around the current location of the
Neches River rose-mallow population; however, funding has not been
secured (Dietz 2011, pers. comm.). The Neches River rose-mallow at
Lovelady is concentrated along a low area leading into a stock pond
(Miller 2011, pers. comm.). Only one of 11 sites (9 percent of the
total known population) has shown damage from cattle herbivory.
Trampling has not been observed at the Lovelady site or any other.
Drought could exacerbate herbivory, as was seen in the severe drought
of 2011, which could lead to an increase in trampling. The immediacy
and severity of herbivory to the Neches River rose-mallow is high, but
the exposure to herbivory is low. Therefore, we conclude that herbivory
is not a
[[Page 56062]]
threat to to the Neches River rose-mallow.
Natural Gas Pipelines and Well Activity
The Haynesville or Bossier and Eagle Ford Shale formations in east
Texas are currently being developed for oil and natural gas production.
The Texas Railroad Commission regulates the oil and natural gas
industry in the State of Texas and maintains a database with proposed
activities. Several of the counties with known populations of Neches
River rose-mallow, including Houston, Trinity, Nacogdoches, and
Cherokee Counties, may be subject to increased oil and natural gas
exploration in the future (Texas Railroad Commission 2012). However,
oil and gas exploration was not observed on or directly adjacent to any
of the Neches River rose-mallow populations that the Service observed
in 2011, and currently there are no proposals near extant Neches River
rose-mallow populations. Therefore, we determine that oil and natural
gas exploration activities are not currently a threat to the Neches
River rose-mallow.
Climate Change
We discuss the topic of climate change in greater detail under ``A.
The Present or Threatened Destruction, Modification, or Curtailment of
Its Habitat or Range'' for the Texas golden gladecress (which, like the
Neches River rose-mallow, is also found in east Texas). In summary, the
consensus of climate models predicts that the climate in east Texas
will become warmer and will experience both more frequent droughts and
more extreme precipitation events. Diggs et al. (2006, p. 80) states
that climate extremes, particularly drought and low temperatures, have
greater influence than average conditions do on excluding nonadapted
species. Extreme precipitation events (such as tropical storms) may
adversely affect the Neches River rose-mallow by altering flow regimes
and by temporarily increasing the depth of its wetland habitat to a
level at which the species cannot survive. A warmer climate with more
precipitation extremes may also increase competition from native and
nonnative invasive plant species (Service 2010b, p. 8). The timing of
precipitation is also crucial for the Neches River rose-mallow, as seed
dispersal is likely dependent on flowing water.
Neches River rose-mallow has shown evidence of damage from drought
conditions. In October 2011, all Neches River rose-mallow populations
and habitats showed evidence of damage from the previous 3 years of
drought, including changes in leaf morphology, dead plants at specific
sites, reduced seed production, and lower water levels in perennial
wetlands. In addition, one site (The Texas Land Conservancy site)
showed evidence of herbivory by livestock. The survival of Neches River
rose-mallow populations during previous drought cycles may have been
aided by its greater abundance and by greater habitat contiguity. Loss
of habitat contiguity impedes the recolonization of sites from
neighboring seed sources following a catastrophic loss, such as from
drought. More frequent droughts will further exasperate these impacts
to the Neches River rose-mallow.
With climate change projections of warmer and more frequent
droughts, and more extreme precipitation events, impacts to the Neches
River rose-mallow will continue. The severity of impacts to the Neches
River rose-mallow is high, as all populations will be impacted.
Further, this threat is current and will continue into the near future.
Other Conservation Efforts
Three populations of the Neches River rose-mallow exist along SH
ROWs in Houston, Trinity, and Cherokee Counties. The TXDOT and TPWD
currently operate under a revised 1988 memorandum of understanding
(MOU) that governs management actions targeting conservation of listed
species and key habitats on SH ROWs that may potentially affect natural
resources within facilities owned or managed by TPWD. Because the
Neches River rose-mallow was not a listed species, the MOU relates to
protection of Neches River rose-mallow habitat if the proposed projects
include the following: Contains 1.0 ac (0.54 ha) of new ROW within
floodplains or creek drainages; requires channel modifications to
streams, rivers, or water bodies; and requires realignment of channels
with mature woody vegetation; or projects that may impact mature woody
or native vegetation (Texas Administrative Code 1999, p. 4). Although a
formal mechanism via the MOU has been established to review projects
and alleviate or eliminate threats to Federal and State-listed species
and key resources, there have not been any projects that fit these
standards that have been recently reviewed under the MOU.
Five populations, including a portion of the SH 94 site, are
located on private lands. Historically, two candidate conservation
agreements were formed between the Service and Champion International
(Champion) in 1998, and with Temple-Inland Forest Products (Temple-
Inland) in 2002, to conserve the Neches River rose-mallow on both
sites. The candidate conservation agreements have expired, and private
landowners are not restricted by guidelines outlined those agreements.
Champion's 5-year candidate conservation agreement included 40 ac (16.2
ha) of wetland and was located east of White Rock Creek in Trinity
County (Champion site in Table 4). Management guidelines included:
Maintain 100-ft (30-m) buffer around occupied and dispersal habitat,
free from timber harvesting, site preparation, and reforestation
activities; minimize hydrological alterations; inhibit filling or
pilling debris or material on populations; and apply herbicides only by
hand and at times of little or no wind (Service 1998, p. 4). The
Champion property was sold to Temple-Inland in 2001, and in 2004, the
candidate conservation agreement expired (Service 2010b, p. 9). The
Temple-Inland candidate conservation agreement covered an area that has
a 20-ac (8.1-ha) wetland with Neches River rose-mallow (Boggy Slough
site in Table 4); the plants declined due to drought and alteration of
an onsite wetland. A smaller wetland with Neches River rose-mallow
plants was drained in order to regulate water levels of the larger
wetland, which was to be used by Temple-Inland for recreational hunting
(Service 2002, p. 3; Service 2010b, p. 9). The Temple-Inland candidate
conservation agreement was valid from 2002-2004. Contact was made with
the owners, and the Service and TPWD visited the site in October 2011.
Plants appeared healthy, but nonnative and native species encroachment
into Neches River rose-mallow habitat was observed (Miller 2011, pers.
comm.).
Four known sites lie within the Davy Crockett NF, which is managed
under the Revised Land and Resource Management Plan. The USFS considers
the Neches River rose-mallow a sensitive species. Actions occurring on
USFS property must not result in a net loss of species viability or
create significant trends toward the need for Federal listing. However,
USFS standards and guidelines in the plan are not mandatory and do not
address all threats pertaining to the Neches River rose-mallow.
The Lovelady site is owned by The Texas Land Conservancy, once
known as the Natural Area Preservation Association. Thirty acres (12
ha) of land were purchased in 2004, located north of SH 230 (The Texas
Land Conservancy 2011). Purchase of this easement on
[[Page 56063]]
private land was specifically for the conservation of the Neches River
rose-mallow; however, plants occur on private land, and they are not
offered protection under the Act unless there is a Federal nexus.
However, The Texas Land Conservancy had initiated a voluntary effort to
construct a cattle-exclusion fence, but funds were lacking and the
project was not completed (Dietz 2011, pers. comm.). The introduced
site at Mill Creek Gardens was created in 1995, as a conservation
easement by a private donor (Stephen F. Austin State University 1999,
p. 1), and was used as an experimental plot to test fertilizer and
mulching effects on the Neches River rose-mallow (Scott 1997, pp. 6-7).
This site is informally managed through mowing and burning regimes
prescribed by Stephen F. Austin State University staff, but
encroachment from native woody species has been observed in the past
(Creech 2011c, pers. comm.). The Neches River rose-mallow was last
observed in 1980 at the Harrison County site and the site has not been
revisted since then due to a lack of accessibility. The Neches River
rose-mallow was last observed at the Camp Olympia site in 1978. The
site has been revisited in 1992 and 1993, but has not been observed
(Warnock 1995, pp. 6, 8; TXNDD 2012a, pp. 58-60). Introductions onto
Mill Creek Gardens and the Pineywoods Native Plant Center on the
Stephen F. Austin State University campus have provided researchers the
opportunities to study the species, including its affinity for
hybridization. Seed has also been collected by the Mercer Arboretum in
Ft. Collins, Colorado.
Summary of Factor A
Based on our evaluation of the best available scientific and
commercial data, we conclude that the present loss and modification of
the Neches River rose-mallow's habitat is a threat that has significant
impacts to the species' continued survival. Threats include competition
for light and nutrients by native and nonnative invasive plant species,
altered hydrology, herbicide drift, and trampling by feral hogs. These
threats may be exacerbated by future road and bridge construction and
maintenance projects. We determine that livestock grazing is not a
threat to the species. Although silvicultural practices have caused
some prior impacts to the species, we do not anticipate that
silviculture activities will continue to be a threat. The activities
related to exploration and development of oil and natural gas wells are
not currently a threat to the species. Effects of climate change may be
exacerbated by effects from other threats. Additional conservation
measures that had protected habitat and certain actions on privately
owned land have expired and no longer provide protection to habitat of
the Neches River rose-mallow. Therefore, we conclude that habitat loss,
destruction, and modification is a threat to the Neches River rose-
mallow rangewide both now and in the future.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
The showy flowers produced by the genus Hibiscus make it of high
horticultural interest (Service 2010b, p. 8) to Hibiscus enthusiasts
(Warnock 1995, p. 25; Poole et al. 2007, p. 265). Hybridization within
genus Hibiscus is repeatedly done in the nursery trade (Creech 2011a,
pers. comm.) to produce different colored flowers and modify other
traits that may be of commercial interest. Ornamental landscaping
companies sell Neches River rose-mallow plants online (Creech 2011a,
pers. comm.). Neches River rose-mallow plants are easy to cultivate
from cuttings, and having plants available for sale in the nursery
trade reduces collecting pressures of the species from the wild (Creech
2011a, pers. comm.). Plantings of Neches River rose-mallow into garden
settings are standard, and placement within close proximity to wild
populations has not been recorded or observed.
Mercer Arboretum collected seed in 1993, 1994, 1996, 1997, and
2003; these seeds, as well as living plants, are being maintained at
the Mercer Arboretum (Tiller 2011, pers. comm.). A portion of the seeds
collected were grown out in the Mercer Arboretum Rare and Endangered
Gardens, where they have remained; seeds and plants have not been
transplanted back into the wild populations (Tiller 2011, pers. comm.).
Neches River rose-mallow seed was also sent to the National Seed
Storage Laboratory in Fort Collins, Colorado, for long-term storage for
conservation purposes (Ellis 2011, pers. comm.).
The scientific and horticultural communities have collected Neches
River rose-mallow seeds and plants from wild populations; however, we
have no evidence that suggests that collection has depleted the seed
bank or has adversely affected populations. Plants are easily
cultivated, and the species is well established as a nursery trade
plant, thereby reducing potential collection pressure. Based on the
best scientific and commercial data available, we conclude that
collection for recreational, scientific, or educational purposes is not
a threat to the Neches River rose-mallow and is not likely to become
one in the future.
C. Disease or Predation
Leaves and stems of plants in the Hibiscus family (Kroll 1991, p.
392; Everitt et al. 1999, pp. 177-193) are often consumed by white-
tailed deer (Odocoileus virginianus) (Moreland 2005, p. 48). Cattle
also consume the stems but typically to a lesser degree than white-
tailed deer (Everitt et al. 1999, pp. 187-193). In 1993, evidence of
herbivory was present at four of the 11 Neches River rose-mallow
subpopulations at Lovelady (Warnock 1995, p. 18) and in 2010, at
compartment 20 (Allen and Duty 2010, p. 3). In 2011, at five of the 11
populations, aboveground portions of the Neches River rose-mallow,
mainly the tips, were grazed by cattle, with the most intense herbivory
occurring at the Lovelady site; cattle on adjacent land were the likely
culprit. Herbivore consumption of plants could decrease the
reproductive success of the Neches River rose-mallow (Adler et al.
2001, p. 1). Only at compartment 20 on the Davy Crockett NF was the
evidence of browsing on the flowers observed (Allen and Duty 2010, p.
3); however, the species is able to produce secondary growth, which
increases and strengthens the girth rather than the height of the plant
(Strauss and Agrawal 1999, p. 179; Bailey 2006, p. 415).
Insect damage and predation has been observed on Neches River rose-
mallow plants in several populations; however, regrowth of foliage
after herbivory incidents may indicate that the Neches River rose-
mallow is adapted to herbivory (Strauss and Agrawal 1999, p. 179).
Ninety percent of the first foliage of Neches River rose-mallow leaves
at Lovelady had been consumed by insects (Service 2010b, p. 8) with
insect predation also seen on compartment 11 plants in 2006 (Philipps
2009, p. 1). The scentless plant bug (Niesthrea louisianica) was
observed on plants in compartment 55 (Miller 2011, pers. comm.). This
bug is known to deposit egg masses on stems, leaves, flower parts,
buds, and seed pods of Hibiscus species (Wheeler 1977, p. 632), but to
also consume Hibiscus seeds (Toth 2007, p. 6). Holes were observed on
several Neches River rose-mallow plants on all Davy Crockett NF sites
(Miller 2011, pers. comm.) and were likely caused by this plant bug.
Larval forms of the Hibiscus sawfly (Atomacera decepta) can consume
Neches River rose-mallow seed pods in herbaria, but have not been noted
to affect wild populations (Wieland 1995, p. 1; Creech
[[Page 56064]]
2011a, pers. comm.). However, these bugs are not considered a
significant pest because the damage to the plants is minor (Toth 2007,
p. 6).
Changes in precipitation are not well understood in relationship to
insect herbivory (Bale et al. 2002, p. 2). Drought conditions may
exacerbate consumption of the vegetative and floral parts if other food
resources within the plant community become scarce. Temperature shifts
related to climate change may trigger corresponding insect population
shifts. Impacts from insect population shifts cannot be predicted;
however, if conditions favor the growth of insect populations, the
effects of insect herbivory on the Neches River rose-mallow could
increase. Drought could exacerbate the consumption of leaves and stems
if preferred plants were not available, but we conclude that ungulate
(hoofed animal) herbivory is an insignificant stressor to the Neches
River rose-mallow.
Summary of Factor C
Mammalian herbivory has affected the majority of sites; however,
grazing pressures are largely attributed to the lack of other available
food resources during periods of drought. Neches River rose-mallow
recovers quickly from herbivory incidents and can produce secondary
growth, minimizing the overall negative effects of mammalian herbivory.
This type of herbivory is not considered to be a threat to the species.
Insect herbivory was also observed on several of the sites and was not
rangewide, but, with anticipated climate change shifts in temperature
and the likelihood that insect populations will increase, we conclude
that insect predation is a minor stressor that will likely continue
into the future, but it is not a threat to the species.
D. The Inadequacy of Existing Regulatory Mechanisms
Under this factor, we examine whether existing regulatory
mechanisms are inadequate to address the threats to the species
discussed under the other factors. Section 4(b)(1)(A) of the Act
requires the Service to take into account ``those efforts, if any,
being made by any State or foreign nation, or any political subdivision
of a State or foreign nation, to protect such species . . . .'' In
relation to Factor D under the Act, we interpret this language to
require the Service to consider relevant Federal, State, and tribal
laws, regulations, and other such mechanisms that may minimize any of
the threats we describe in threat analyses under the other four
factors, or otherwise enhance conservation of the species. We give
strongest weight to statutes and their implementing regulations and to
management direction that stems from those laws and regulations. An
example would be State governmental actions enforced under a State
statute or constitution, or Federal action under statute.
Having evaluated the significance of the threat as mitigated by any
such conservation efforts, we analyze under Factor D the extent to
which existing regulatory mechanisms are inadequate to address the
specific threats to the species. Regulatory mechanisms, if they exist,
may reduce or eliminate the impacts from one or more identified
threats. In this section, we review existing State and Federal
regulatory mechanisms to determine whether they effectively reduce or
remove threats to the Neches River rose-mallow.
Davy Crockett NF lands are federally owned and managed by the USFS
for the general public. Four populations of the Neches River rose-
mallow occur on the Davy Crockett NF. The Davy Crockett NF classifies
the Neches River rose-mallow as a Regional Forester's Sensitive Species
(Philipps 2012, pers. comm.), and habitat is within Management Area
Zone 4, according to the Revised Land and Resource Management Plan for
National Forests and Grasslands in Texas (USDA 1996, entire). This
management zone includes the bed, bank, and water resources of the
rivers, perennial and intermittent streams and wetlands, and their
adjacent areas (United States Department of Agriculture 1996, p. 145).
This area is managed to maintain the role and function of aquatic,
riparian, and wetland ecosystems while providing opportunities for
compatible multiple uses and will be managed to meet recommendations
stated in the Texas Wetland Plan (TPWD 1988) and Best Management
Practices established by the State (United States Department of
Agriculture 1996, p. 151). Relative Management Area Zone 4 standards
and guidelines include: Maintenance or restoration of native plant
communities; prohibition of nonaquatic herbicide uses, except hand
applications or noxious weed control following restriction on the
herbicide label; and use of prescribed fire when necessary to enhance
riparian vegetation or wildlife habitat (United States Department of
Agriculture 1996, pp. 153, 155). Herbicides are not currently being
used on the Davy Crockett NF and have been replaced by prescribed fire,
with the goal of routinely burning compartments every 3 years (Stiles
2011, pers. comm.). As discussed previously (see ``Nonnative Species''
under the Factor A discussion), routine fires may play a role in
reducing Chinese tallow. Actions that may affect Neches River rose-
mallow habitat need to be assessed using these standards and guidelines
because these are considered regulations that need to be followed
(Philipps 2012, pers. comm.). The encroachment of nonnative and native
vegetation in Neches River rose-mallow habitat is not addressed in the
Revised Land and Resource Management Plan for National Forests and
Grasslands in Texas; however, the application of prescribed fire in
some areas may benefit the Neches River rose-mallow.
The Neches River rose-mallow is considered by the USFS to be a
sensitive species on the Davy Crockett NF. A sensitive species is
defined as one not yet warranting listing as an endangered or
threatened species, but which is sufficiently rare that its future
survival is of concern (USFS Manual 2670, 2005). The management
objectives described in USFS Manual 2670 are to develop and implement
management practices to ensure that species do not become endangered or
threatened because of USFS actions, including: Maintain viable
populations of all native and desired nonnative wildlife, fish, and
plant species in habitats distributed throughout their geographic range
on NF System lands; and develop and implement management objectives for
populations or habitat of sensitive species or both. Application of
USFS Manual 2670 standards are only guidelines, and are not mandatory.
However, the USFS must consider the effects of their actions on the
viability of sensitive species through the National Environmental
Policy Act (NEPA; 42 U.S.C. 4321 et seq.) process. As defined by USFS
policy, actions must not result in loss of species viability or create
significant trends toward the need for Federal listing. This
designation does not provide specific habitat or species protection,
but does provide some benefits to the species because of increased
awareness and evaluating projects that may affect the species through
the NEPA process. Specific threats to the Neches River rose-mallow are
not addressed with this designation.
Existing regulatory mechanisms do not provide protection for plants
on private lands. Neches River rose-mallow populations on Davy Crockett
NF lands only receive some protection from habitat modification. In
addition, not all threats are addressed, such as encroachment of
nonnative and native species into Neches River rose-mallow habitat. The
designation as a sensitive species for the Neches River rose-mallow
does not address the threats
[[Page 56065]]
specific to the species. Only when the species is listed under the Act
will the USFS be required to consult on projects that could impact the
species or its habitat. Therefore, based on our review of the best
scientific and commercial data available, we conclude that existing
regulatory mechanisms provide some protection against threats, but
these mechanisms do not address or ameliorate all of the threats.
E. Other Natural or Manmade Factors Affecting Its Continued Existence
Small Population Size
Small population size can result in a decrease in genetic diversity
due to genetic drift (the random change in genetic variation each
generation) and inbreeding (mating of related individuals) (Antonovics
1976, p. 238; Ellstram and Elam 1993, pp. 218-219). Genetic drift can
decrease genetic variation within a population by favoring certain
characteristics and, thereby, increasing differences between
populations (Ellstram and Elam 1993, pp. 218-219). Self-fertilization
and low dispersal rates can cause low genetic diversity due to
inbreeding (Antonovics 1976, p. 238; Barrett and Kohn 1991, p. 21).
This decreased genetic diversity diminishes a species' ability to adapt
to the selective pressures of a changing environment (Ellstrand 1992,
p. 77; Newman and Pilson 1997, p. 360).
Klips (1995) looked at the genetic affinity of the Neches River
rose-mallow compared with the two other congeners (similar) species,
Hibiscus moscheutos and H. laevis. In his study, Klips concluded both
H. dasycalyx and H. laevis are genetically more similar than H.
moscheutos. Mendoza created the genetic fingerprints for all three
congener species to help determine the level of hybridization within
and among populations. Both studies observed wild plants that appeared
to be hybrids; however, neither Klips nor Mendoza studied the
occurrence of hybridization among the populations of the Neches River
rose-mallow. There is no evidence that Neches River rose-mallow
populations are experiencing genetic drift or inbreeding. We conclude
that small population size is not a threat to the Neches River rose-
mallow.
Hybridization
The genus Hibiscus easily hybridizes in the nursery trade (Creech
2011a, pers. comm.). Hybridization under natural conditions has not
been verified, but several Neches River rose-mallow sites contain
individuals that may be products of crosses between the Neches River
rose-mallow with H. laevis or H. moscheutos. In some locations, H.
laevis or H. moscheutos, or both, grow in close proximity to the Neches
River rose-mallow. These plants have leaves, flowers, and floral parts
resembling both parent species (Service 2010b, p. 3; TXNDD 2012a,
entire). Other species accounts, including our candidate notices of
review and anecdotal accounts from USFS, TPWD, and other botanists,
conclude that there is the potential that hybrids may exist at most, if
not all, of the sites; however, genetic studies have not confirmed that
this phenomenon is occurring. So far, these are only observations, and
no genetic studies have taken place to verify if hybridization is
occurring. The University of Texas-Tyler is researching the
hybridization issue for Neches River rose-mallow and its impacts on the
population; however, the project is only in its infancy, and no results
have been determined. Therefore, we do not consider hybridization to be
a threat to the Neches River rose-mallow.
Conservation Efforts To Reduce Other Natural or Manmade Factors
Affecting Its Continued Existence
We have several examples of voluntary conservation efforts that are
currently underway, or which took place in the past, that directly, or
indirectly, assist the Neches River rose-mallow by addressing the
impacts of habitat loss and degradation, or low population and
individual plant numbers. See description under the Factor A analysis
above.
Cumulative Effects From Factors A Through E
The threats that have the most severe impacts to the Neches River
rose-mallow and its habitat involve the loss, destruction,
modification, and curtailment of habitat. The rangewide and imminent
threat from nonnative species encroachment (mainly Chinese tallow) and
native woody species (sweetgum and green ash) will likely continue if
regulatory mechanisms are not employed. Alteration of natural
hydrological features of Neches River rose-mallow is an ongoing and
potential threat, having rangewide impacts. Trampling and herbivory
also impact the Neches River rose-mallow.
Threats discussed in this finding could work in concert with one
another to cumulatively create situations that potentially impact
Neches River rose-mallow beyond the scope of the combined threats that
we have already analyzed. Specifically, threats may be exacerbated by
the effects of ongoing and future climate change, especially the
projected increases in temperature and decreases in precipitation that
may increase the frequency and severity of droughts. Although the
Neches River rose-mallow is adapted to being dry during portions of the
year, a complete lack of water can diminish its ability to expand its
known range and reduce its genetic exchange. Further, climate change
could lead to an increase in nonnative species, because nonnative
species can typically tolerate a wider range of habitat conditions
outside of those that are suitable for the Neches River rose-mallow.
Drought conditions can increase the susceptibility of sites to be
impacted from trampling from feral hogs, such that observations of
broken and flattened plants would increase. The reproductive
capabilities of feral hogs and their ubiquitous foraging behavior
allows them to adapt well to drought conditions. Herbivory from cattle,
or white-tail deer, would also increase in concert with future effects
of climate change. Hydrological alterations combined with drought
conditions could cause or intensify herbivory. This phenomenon was only
observed at The Texas Land Conservancy site in 2011 by cattle, where
drought likely increased the grazing pressures not normally experienced
by the Neches River rose-mallow within this site. A reduction in the
height of Neches River rose-mallow stems could increase its
vulnerability to browsing by cattle. The drought conditions of 2011
caused decreased heights in Neches River rose-mallow plants; this,
combined with the lack of a cattle exclusion fence on an adjacent land
to The Texas Land Conservancy, likely increased the risk of herbivory.
When normal rainfall resumes and preferred forage sources become
available, herbivory would likely decrease.
Summary of Factors
The primary factors threats to Neches River rose-mallow are
nonnative species encroachment at all sites; invasion of sites by
native woody species, causing shading and increased competition for
resources; ongoing and potential changes to key hydrological features
of the species' habitat; future construction and ROW projects; and
aerial herbicide drift incidents. These factors pose imminent threats
to the species because they are ongoing or are likely to occur in the
near future. Since the Neches River rose-mallow is endemic to
intermittent and perennial wetlands, drought can exacerbate all of the
existing threats.
Determination
Based on our review of the best scientific and commercial data
[[Page 56066]]
available, we conclude that the Neches River rose-mallow is likely to
become an endangered species within the foreseeable future and,
therefore, meets the definition of a threatened species. This finding,
explained below, is based on our conclusions that the Neches River
rose-mallow's primary threats are imminent, thus causing the species to
exhibit low viability as characterized as having only one site close to
meeting its conservation goals. Significant factors that support this
determination include the following:
The significant and ongoing threat from nonnative species
at all sites (Factor A);
The encroachment of habitat from woody natives (Factor A);
The potential extirpation of an occupied Neches River
rose-mallow site from a reservoir project (Factor A);
Ongoing and potential changes to key hydrological features
of the species' habitat (Factor A);
The potential threat from future construction and ROW
projects (Factor A);
The trampling from feral hogs (Factor A);
Ongoing threats from aerial herbicide drift incidents
(Factor A); and
Sustained drought that affects habitat quality and
reproductive output of the species (Factor A).
We relied on Pavlik's Minimum Viable Population analysis tool
(1996, pp. 127-155) and species experts to determine the conservation
goals of the species. Based on the best known and available scientific
information on the species' life-history and reproductive
characteristics, we concluded that the conservation goals for the
Neches River rose-mallow included 10 viable populations, each
containing at least 1,400 individual plants. The species is limited to
the Neches, Sabine, and Angelina River basins and the Mud and
Tantabogue Creek basins with 11 extant sites throughout this range.
However, many of these sites were introduced and are now compromised by
threats from feral hog damage, hydrological changes, nonnative and
native species encroachment into habitat, construction projects, and
herbicide overspray. Future management actions that ameliorate these
threats could allow for the species to expand within its known range.
The extant populations are generally small. The only site that has come
close to reaching the conservation goals are on compartment 55 of the
USFS; however, it still only comprises 53 percent of the needed plants
at this site (750 plants were seen in 2010).
The main sources of habitat loss, degradation, and modification
include hydrologic changes (which alter habitat suitability, growth of
plants, expansion into new areas, and potentially seed dispersal);
encroachment of habitat from woody natives and invasive nonnatives
(which out-shade and compete for nutrients and water absorption); road
construction and maintenance projects; aerial drift of herbicides
(which may go unregulated on private lands); trampling by feral hogs
(known to flatten and break plants); and herbivory. These can have a
cumulative impact that further depletes population numbers. Drought is
likely to exacerbate these threats.
Most threats are distributed across the geographic range of the
Neches River rose-mallow. These threats include: Encroachment by woody
natives and invasive nonnatives, hydrological changes, and trampling.
The threat from nonnatives is imminent and is occurring at all
populations, resulting in competition for light and nutrients, but
maintenance activities occur within some populations to minimize this
threat. Although information on populations inhabiting private lands is
a bit lacking, some degree of hydrological change has been seen at most
sites and is therefore rangewide. This threat is likely to continue
into the future as water resources become more scarce and important to
the human population. Drought will likely exacerbate existing threats
and impact all populations. Direct impacts to plants from trampling has
been documented at 4 of the 11 Neches River rose-mallow sites, and
several others have had documented observations of damaged habitat from
feral hog tracks. However, some threats do not affect all Neches River
rose-mallow populations. For instance, drift from herbicide spraying
likely resulted in the extirpation of the Neches River rose-mallow in
the SH 230 ROW, and the other two populations within SH ROWs may be
affected by herbicide spraying in the future; however, Neches River
rose-mallow populations on NF lands are not threatened by this
activity. To our knowledge, this species has not experienced a
reduction in its range, all of the known populations and sites are
still present on the landscape, and the natural populations have
maintained viable population numbers. In addition, there are four
introduced populations that remain viable, although the introduced
populations on USFS lands have declined in recent years. Some threats
are likely to occur in the near future, but are not ongoing. The
potential effects from the construction of the Lake Columbia reservoir
have not taken place, and there is uncertainty if the downstream
population of Neches River rose-mallow would be affected by changes in
hydrology. Therefore, we conclude that the species does not meet the
definition of an endangered species (in danger of extinction throughout
all or a significant portion of its range), but meets the definition of
a threatened species (likely to become an endangered species in the
foreseeable future throughout all or a significant portion of its
range).
We evaluated whether the Neches River rose-mallow is in danger of
extinction now (i.e., an endangered species) or is likely to become in
danger of becoming endangered (i.e., a threatened species) in the
foreseeable future. The foreseeable future refers to the extent to
which the Secretary can reasonably rely on predictions about the future
in making determinations about the conservation status of the species.
A key statutory difference between an endangered species and a
threatened species is the timing of when a species may be in danger of
extinction, now (endangered) or in the foreseeable future (threatened
species).
In the case for the Neches River rose-mallow, the best available
scientific information indicates that, while reductions in the species'
range have not occurred, there have been significant impacts from
habitat modification and loss that has caused reductions in most, if
not all, of the known Neches River rose-mallow populations. However,
there are sufficient numbers of populations available, some of which
are being conserved for the Neches River rose-mallow. Four of the 11
existing Neches River rose-mallow populations, including the largest
and most robust population, occur on USFS lands. However, the USFS
Revised Land and Resource Management Plant does not address all the
significant threats to the species. The Texas Land Conservancy private
land site was purchased as a conservation easement for the Neches River
rose-mallow. However, these protection measures are voluntary. We
conclude that the Neches River rose-mallow is likely to become an
endangered species within the foreseeable future, meeting the standard
of a threatened species.
The Act defines threatened as ``any species that is likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range.'' A major part of the
analysis of ``significant portion of the range'' requires considering
whether the threats to the Neches River rose-mallow are geographically
concentrated in any way.
[[Page 56067]]
If the threats are consistently uniform throughout the species' range,
then no portion is likely to warrant further consideration.
As threats extend throughout the species' entire range and are not
geographically concentrated, it is unnecessary to determine whether the
Neches River rose-mallow should be considered an endangered species
within a significant portion of its range. Therefore, on the basis of
the best available scientific and commercial information, we are
listing the Neches River rose-mallow as a threatened species throughout
its range in accordance with sections 3(20) and 4(a)(1) of the Act.
Available Conservation Measures
Conservation measures provided to species listed as an endangered
or threatened species under the Act include recognition, recovery
actions, requirements for Federal protection, and prohibitions against
certain practices. Recognition through listing results in public
awareness and conservation by Federal, State, tribal, and local
agencies; private organizations; and individuals. The Act encourages
cooperation with the States and requires that recovery actions be
carried out for all listed species. The protection required by Federal
agencies and the prohibitions against certain activities are discussed,
in part, below.
The primary purpose of the Act is the conservation of endangered
and threatened species and the ecosystems upon which they depend. The
ultimate goal of such conservation efforts is the recovery of these
listed species, so that they no longer need the protective measures of
the Act. Subsection 4(f) of the Act requires the Service to develop and
implement recovery plans for the conservation of endangered and
threatened species. The recovery planning process involves the
identification of actions that are necessary to halt or reverse the
species' decline by addressing the threats to its survival and
recovery. The goal of this process is to restore listed species to a
point where they are secure, self-sustaining, and functioning
components of their ecosystems.
Recovery planning includes the development of a recovery outline
shortly after a species is listed, preparation of a draft and final
recovery plan, and revisions to the plan as significant new information
becomes available. The recovery outline guides the immediate
implementation of urgent recovery actions and describes the process to
be used to develop a recovery plan. Revisions of the plan may be done
to address continuing or new threats to the species, as new substantive
information becomes available. The recovery plan identifies site-
specific management actions that will achieve recovery of the species,
measurable criteria that determine when a species may be downlisted or
delisted, and methods for monitoring recovery progress. Recovery plans
also establish a framework for agencies to coordinate their recovery
efforts and provide estimates of the cost of implementing recovery
tasks. Recovery teams (comprising species experts, Federal and State
agencies, nongovernmental organizations, and stakeholders) are often
established to develop recovery plans. When completed, the recovery
outline, draft recovery plan, and the final recovery plan will be
available on our Web site (https://www.fws.gov/endangered), or from our
Texas Coastal Ecological Services Field Office in Corpus Christi (see
ADDRESSES, above).
Implementation of recovery actions generally requires the
participation of a broad range of partners, including other Federal
agencies, States, tribes, nongovernmental organizations, businesses,
and private landowners. Examples of recovery actions include habitat
restoration (e.g., restoration of native vegetation), research, captive
propagation and reintroduction, and outreach and education. The
recovery of many listed species cannot be accomplished solely on
Federal lands because their range may occur primarily or solely on non-
Federal lands. To achieve recovery of these species requires
cooperative conservation efforts on private, State, and tribal lands.
Once these species are listed, funding for recovery actions will be
available from a variety of sources, including Federal budgets, State
programs, and cost share grants for non-Federal landowners, the
academic community, and nongovernmental organizations. In addition,
pursuant to section 6 of the Act, the State of Texas would be eligible
for Federal funds to implement management actions that promote the
protection and recovery of the Texas golden gladecress and the Neches
River rose-mallow. Information on our grant programs that are available
to aid species recovery can be found at: https://www.fws.gov/grants.
Please let us know if you are interested in participating in
recovery efforts for the Texas golden gladecress and the Neches River
rose-mallow. Additionally, we invite you to submit any new information
on this species whenever it becomes available and any information you
may have for recovery planning purposes (see FOR FURTHER INFORMATION
CONTACT).
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is proposed or listed as
endangered or threatened and with respect to its critical habitat, if
any is designated. Regulations implementing this interagency
cooperation provision of the Act are codified at 50 CFR part 402.
Section 7(a)(4) of the Act requires Federal agencies to confer with the
Service on any action that is likely to jeopardize the continued
existence of a listed species or result in destruction or adverse
modification of critical habitat. If a species is listed subsequently,
section 7(a)(2) of the Act requires Federal agencies to ensure that
activities they authorize, fund, or carry out are not likely to
jeopardize the continued existence of the species or destroy or
adversely modify its critical habitat. If a Federal action may affect a
listed species or its critical habitat, the responsible Federal agency
must enter into consultation with the Service.
For the Texas golden gladecress, Federal agency actions that may
require consultation would include federally funded or permitted
actions occurring within the species' habitat, specifically within the
zone of Weches outcrops in Sabine and San Augustine Counties.
Anticipated actions include: (1) Provision of Federal financial and
technical assistance through the U.S. Department of Agriculture; (2)
permits issued by the Federal Energy Regulatory Commission for
installation of interstate natural gas pipelines and associated
infrastructure; (3) provision of Federal Highway Administration funds
for road projects; (4) provision of Department of Housing and Urban
Development funds for municipal and residential construction and
infrastructure projects in towns along SH 21 within the range of the
Texas golden gladecress; (5) funds for electric service improvements
provided to electric cooperatives by the U.S. Department of
Agriculture's Rural Utilities Service; (6) U.S. Army Corps of Engineers
(USACE)-issued section 404 and section 10 permits for wetland crossings
that are part of linear projects such as roads, transmission lines, or
pipelines; and (7) actions funded by the Federal Emergency Management
Agency. Also subject to consultation would be provision of Federal
funds to State and private entities through Federal programs such as
the Service's Partners for Fish and Wildlife Program, State Wildlife
Grant Program, and Federal Aid in Wildlife Restoration Program.
[[Page 56068]]
For the Neches River rose-mallow, Federal agency actions that may
require consultation would include federally funded or permitted
actions occurring within the species habitat. These actions could
include: (1) New construction and maintenance of roads or highways by
the Federal Highway Administration; (2) issuance of section 404 Clean
Water Act (33 U.S.C. 1251 et seq.) and section 10 permits by the USACE
for federally funded activities within Federal jurisdictional wetlands;
(3) management and any other landscape-altering activities on Federal
lands administered by the Fish and Wildlife Service and U.S. Department
of Agriculture's USFS; and (4) Federal Highway Administration funds
given to TXDOT for SH ROW maintenance.
The Act and its implementing regulations set forth a series of
general prohibitions and exceptions that apply to endangered and
threatened plants. The prohibitions of section 9(a)(2) of the Act,
codified at 50 CFR 17.61, apply to endangered plants. These
prohibitions, in part, make it illegal for any person subject to the
jurisdiction of the United States to import or export, transport in
interstate or foreign commerce in the course of a commercial activity,
sell or offer for sale in interstate or foreign commerce, or remove and
reduce the species to possession from areas under Federal jurisdiction.
In addition, for plants listed as endangered, the Act prohibits the
malicious damage or destruction on areas under Federal jurisdiction and
the removal, cutting, digging up, or damaging or destroying of such
plants in knowing violation of any State law or regulation, including
State criminal trespass law. It is also unlawful to violate any
regulation pertaining to plant species listed as endangered or
threatened (section 9(a)(2)(E) of the Act).
Chapter 88 of the Texas Parks and Wildlife Code lists plant species
as State endangered or threatened, with the same status as the Federal
designation, immediately upon completion of final Federal listing. The
State prohibits commerce in endangered or threatened plants and the
collection of listed plant species from public land (defined as State-
owned and land belonging to local governments) without a permit issued
by TPWD. The State also prohibits removal for purposes of commercial
sale, possession for commercial sale, transport for commercial sale, or
sale of all or part of a listed plant from private land without a
permit issued under Texas Parks and Wildlife Code, section 88.0081. The
TPWD requires commercial permits for the commercial use of listed
plants collected from private land. Scientific permits are required for
collection of endangered plants or plant parts from public lands for
scientific or education purposes.
We may issue permits to carry out otherwise prohibited activities
involving endangered and threatened wildlife species under certain
circumstances. Regulations governing permits are codified at 50 CFR
17.62 for endangered plants, and at 17.72 for threatened plants. With
regard to endangered plants, a permit must be issued for the following
purposes: For scientific purposes or to enhance the propagation or
survival of the species.
It is our policy, as published in the Federal Register on July 1,
1994 (59 FR 34272), to identify to the maximum extent practicable at
the time a species is listed, those activities that would or would not
constitute a violation of section 9 of the Act. The intent of this
policy is to increase public awareness of the effect of a listing on
proposed and ongoing activities within the range of listed species. The
following activities could potentially result in a violation of section
9 of the Act; this list is not comprehensive:
(1) Unauthorized collecting, handling, possessing, selling,
delivering, carrying, or transporting of the Texas golden gladecress or
the Neches River rose-mallow, including import or export across State
lines and international boundaries, except for properly documented
antique specimens of these taxa at least 100 years old, as defined by
section 10(h)(1) of the Act.
(2) Unauthorized removal, damage, or destruction of Texas golden
gladecress or Neches River rose-mallow plants from populations located
on State-owned land (highway ROWs) or on land owned by local
governments.
(3) Unauthorized removal, damage, or destruction of Texas golden
gladecress or Neches River rose-mallow plants on private land in
violation of any State regulation, including criminal trespass.
(4) Unauthorized removal, damage, or destruction of Texas golden
gladecress or Neches River rose-mallow plants from populations located
on federally owned lands.
Questions regarding whether specific activities would constitute a
violation of section 9 of the Act should be directed to the Texas
Coastal Ecological Services Field Office in Corpus Christi (see FOR
FURTHER INFORMATION CONTACT). Requests for copies of the regulations
concerning listed species and general inquiries regarding prohibitions
and permits may be addressed to the U.S. Fish and Wildlife Service,
Endangered Species Permits, 6300 Ocean Drive, Unit 5837, Corpus
Christi, TX 78412-5837 (telephone 361-994-9005; facsimile 361-994-
8262).
Upon listing the Texas golden gladecress and the Neches River rose-
mallow under the Act, the State of Texas's Endangered Species Act
(Texas Administrative Code Chapter 88:88.001-88.012) is automatically
invoked. The State's Endangered Species Act would prohibit commerce in
endangered or threatened plants and the collection of listed plant
species from public land without a permit issued by TPWD and would
restrict any take for commercial purposes from private land to
individuals possessing a permit issued under section 88.0081. The
State's law would also encourage conservation by State government
agencies. Further, the State may enter into agreements with Federal
agencies to administer and manage any area required for the
conservation, management, enhancement, or protection of endangered
species. Funds for these activities could be made available under
section 6 of the Act (Cooperation with the States). Thus, some Federal
protection afforded to these species by listing them (Texas golden
gladecress as endangered, and Neches River rose-mallow as threatened)
will be reinforced and supplemented by protection under State law.
Under section 4(d) of the Act, the Secretary of the Interior has
discretion to issue such regulations as he deems necessary and
advisable to provide for the conservation of threatened species. Our
implementing regulations (50 CFR 17.71) for threatened plants generally
incorporate the prohibitions of section 9 of the Act for endangered
plants, except under certain circumstances, such as when a ``special
rule'' promulgated under section 4(d) of the Act has been issued with
respect to a particular threatened species. In such a case, the general
prohibitions in 50 CFR 17.61 would not apply to that species, and
instead, the special rule would define specific take prohibitions and
exceptions, which we consider necessary and advisable to conserve the
species, that would apply for that particular threatened species. With
respect to a threatened plant, the Secretary of the Interior also has
the discretion to prohibit by regulation any act prohibited by section
9(a)(2) of the Act. Exercising this discretion, which has been
delegated to the Service by the Secretary, the Service has developed
general prohibitions that are appropriate for most threatened plants in
50 CFR 17.71 and exceptions to those prohibitions in 50 CFR 17.72. We
are not promulgating a special section 4(d)
[[Page 56069]]
rule, and as a result, all of the section 9 prohibitions, including the
``take'' prohibitions, will apply to the Neches River rose-mallow.
Required Determinations
National Environmental Policy Act (42 U.S.C. 4321 et seq.)
We have determined that environmental assessments and environmental
impact statements, as defined under the authority of the National
Environmental Policy Act (NEPA; 42 U.S.C. 4321 et seq.), need not be
prepared in connection with listing a species as an endangered or
threatened species under the Endangered Species Act. We published a
notice outlining our reasons for this determination in the Federal
Register on October 25, 1983 (48 FR 49244).
References Cited
A complete list of references cited in this rulemaking is available
on the Internet at https://www.regulations.gov at Docket No. FWS-R2-ES-
2012-0064 and upon request from the Texas Coastal Ecological Services
Field Office in Corpus Christi (see FOR FURTHER INFORMATION CONTACT).
Authors
The primary authors of this package are the staff of the Texas
Coastal Ecological Services Field Office in Corpus Christi.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Transportation.
Regulation Promulgation
Accordingly, we amend part 17, subchapter B of chapter I, title 50
of the Code of Federal Regulations, as set forth below:
PART 17--[AMENDED]
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; and 4201-4245, unless
otherwise noted.
2. Amend Sec. 17.12(h) by adding entries for ``Hibiscus
dasycalyx'' and ``Leavenworthia texana'' to the List of Endangered and
Threatened Plants in alphabetical order under ``Flowering Plants'', to
read as follows:
Sec. 17.12 Endangered and threatened plants.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species
------------------------------------------------------ Historic range Family Status When listed Critical Special
Scientific name Common name habitat rules
--------------------------------------------------------------------------------------------------------------------------------------------------------
Flowering Plants
* * * * * * *
Hibiscus dasycalyx.............. Neches River rose- U.S.A. (TX)........... Malvaceae............ T 814 17.96(a) NA
mallow.
* * * * * * *
Leavenworthia texana............ Texas golden U.S.A. (TX)........... Brassicaceae......... E 814 17.96(a) NA
gladecress.
* * * * * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * *
Dated: August 29, 2013.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2013-22085 Filed 9-10-13; 8:45 am]
BILLING CODE 4310-55-P