Endangered and Threatened Wildlife and Plants; Listing Ipomopsis polyantha, 35721-35746 [2010-15251]
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Federal Register / Vol. 75, No. 120 / Wednesday, June 23, 2010 / Proposed Rules
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DEPARTMENT OF THE INTERIOR
FOR FURTHER INFORMATION CONTACT:
Robin Biscaia, RCRA Waste
Management Section, Office of Site
Remediation and Restoration (OSRR 07–
1), EPA New England—Region 1, 5 Post
Office Square, Suite 100, Boston, MA
02109–3912, telephone number: (617)
918–1642; fax number: (617) 918–0642,
e-mail address: biscaia.robin@epa.gov.
[Docket No. FWS-R6-ES-2010-0015]
[MO 92210-0-0008-B2]
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‘‘Rules and Regulations’’ section of this
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these changes by an immediate final
rule. EPA did not make a proposal prior
to the immediate final rule because we
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preamble to the immediate final rule.
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comment on this action, you should do
so at this time.
SUPPLEMENTARY INFORMATION:
Dated: June 8, 2010.
Ira W. Leighton,
Acting Regional Administrator, EPA New
England.
[FR Doc. 2010–15256 Filed 6–22–10; 8:45 am]
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Fish and Wildlife Service
50 CFR Part 17
RIN 1018-AV83
Endangered and Threatened Wildlife
and Plants; Listing Ipomopsis
polyantha (Pagosa Skyrocket) as
Endangered Throughout Its Range,
and Listing Penstemon debilis
(Parachute Beardtongue) and Phacelia
submutica (DeBeque Phacelia) as
Threatened Throughout Their Range
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), propose to
list Ipomopsis polyantha (Pagosa
skyrocket), a plant species from
southwestern Colorado, as endangered
throughout its range, and Penstemon
debilis (Parachute beardtongue) and
Phacelia submutica (DeBeque phacelia),
two plant species from western
Colorado, as threatened throughout their
ranges under the Endangered Species
Act of 1973, as amended (Act). This
proposal, if made final, would extend
the Act’s protections to these species
throughout their ranges. The Service
seeks data and comments from the
public on this proposal.
DATES: We will consider comments
received or postmarked on or before
August 23, 2010. We must receive
requests for public hearings, in writing,
at the address shown in the FOR FURTHER
INFORMATION CONTACT section by August
9, 2010.
ADDRESSES: You may submit comments
by one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments
on Docket No. FWS-R6-ES-2010-0015.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: [FWS-R6ES-2010-0015]; Division of Policy and
Directives Management; U.S. Fish and
Wildlife Service; 4401 N. Fairfax Drive,
Suite 222, Arlington, VA 22203.
We will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see the
Public Comments section below for
more information).
FOR FURTHER INFORMATION CONTACT:
Patty Gelatt, Acting Western Colorado
Supervisor, U.S. Fish and Wildlife
Service, Ecological Services Field
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35721
Office, 764 Horizon Drive, Building B,
Grand Junction, CO 81506-3946;
telephone 970-243-2778, extension 26;
fax 970-245-6933. If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Public Comments
We intend that any final action
resulting from this proposed rule will be
based on the best scientific and
commercial data available and be as
accurate and as effective as possible.
Therefore, we request comments or
information from the public, other
government agencies, the scientific
community, industry, or any other
interested party concerning this
proposed rule. We particularly seek
comments concerning:
(1) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to these species
and regulations that may be addressing
those threats;
(2) Additional information concerning
the range, distribution, and population
sizes of these species, including the
locations of any additional occurrences
of these species;
(3) Any information on the biological
or ecological requirements of these
species;
(4) Current or planned activities in the
areas occupied by these species and
possible impacts of these activities on
these species;
(5) Which areas would be appropriate
as critical habitat for these species and
why they should be proposed for
designation as critical habitat; and
(6) The reasons why areas should or
should not be designated as critical
habitat as provided by section 4 of the
Act (16 U.S.C. 1531 et seq.), including
whether the benefits of designation
would outweigh threats to these species
that designation could cause, such that
the designation of critical habitat is
prudent.
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in the
ADDRESSES section. We will not
consider comments sent by e-mail or fax
or to an address not listed in the
ADDRESSES section.
We will post your entire comment—
including your personal identifying
information—on https://
www.regulations.gov. If you provide
personal identifying information in your
hardcopy comments, you may request at
the top of your document that we
withhold this information from public
review. However, we cannot guarantee
that we will be able to do so. We will
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post all hardcopy comments on https://
www.regulations.gov.
Comments and materials we receive,
as well as supporting documentation we
used in preparing this proposed rule,
will be available for public inspection
on https://www.regulations.gov, or by
appointment, during normal business
hours, at the U.S. Fish and Wildlife
Service, Western Colorado Ecological
Services Field Office (see FOR FURTHER
INFORMATION CONTACT section).
Final promulgation of the regulations
concerning the listing of these species
will take into consideration all
comments and additional information
that we receive, and may lead to a final
regulation that differs from this
proposal.
Species Information and Factors
Affecting the Species
Section 4 of the Act (16 U.S.C. 1533)
and implementing regulations (50 CFR
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, 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.
Below is a species-by-species analysis
of these five factors. The species are
considered in the following order:
Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica.
Background—Ipomopsis polyantha
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Previous Federal Actions
We first identified Ipomopsis
polyantha as a taxon under review in
the 1983 Supplement to Review of Plant
Taxa for Listing as Endangered or
Threatened Species (48 FR 53640,
November 28, 1983). In that document,
we included the species as a Category 2
candidate, based on our evaluation at
that time. Category 2 candidate species
were formerly defined as ‘‘taxa for
which information now in the
possession of the Service indicates that
proposing to list the taxa as Endangered
or Threatened species is possibly
appropriate, but for which sufficient
data on biological vulnerability and
threat(s) are not currently known or on
file to support proposed rules’’ (48 FR
53641, November 28, 1983). We
published our decision to discontinue
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candidate categories and to restrict
candidate status to those taxa for which
we have sufficient information to
support issuance of a proposed rule on
December 5, 1996 (61 FR 64481), This
resulted in the deletion of Ipomopsis
polyantha from the list of candidate taxa
for listing. Since 1996, threats to the
species have become more numerous
and more widespread. We added the
species to the list of candidates again in
the 2005Candidate Notice of Review
(CNOR) (70 FR 24873, May 11, 2005)
with a listing priority number (LPN) of
2. Candidates are taxa for which we
have sufficient information on
biological vulnerability and threats to
support preparation of a listing
proposal, but for which development of
a listing regulation is precluded by other
higher priority listing activities.
Candidate species are assigned an LPN
(1-12, with 1 being the highest priority)
based on magnitude and immediacy of
threats and taxonomic status. A listing
priority of 2 reflects threats that are
imminent and high in magnitude, as
well as the taxonomic classification of I.
polyantha as a full species. We
published a complete description of our
listing priority system in the Federal
Register (48 FR 43098, September 21,
1983).
Species Information
Ipomopsis polyantha is a rare plant
endemic to shale outcrops in and
around Pagosa Springs in Archuleta
County, Colorado. Suitable habitat for
the species is identified on about 191
acres (ac) (77 hectares (ha)) on the east
edge of town, and on about 23 ac (9 ha)
approximately 10 miles (mi) (16
kilometers (km)) west of town.
Approximately 9 percent of the suitable
habitat is on land managed by the
Bureau of Land Management (BLM)
land, 12 percent on State and County
highway rights-of-way (ROWs), 78
percent on private lands, and less than
1 percent on Pagosa Springs park land
and county land (Colorado Natural
Areas Program (CNAP) 2007, pp. 1-5;
Lyon 2005, pp. 1-5; Lyon 2006a, pp. 12; Lyon 2006b, p. 1).
The Colorado Natural Heritage
Program (CNHP) ranks Ipomopsis
polyantha as critically imperiled
globally (G1) and in the State of
Colorado (S1) (CNHP 2006a, p. 1). The
Nature Conservancy (TNC) and CNHP
also developed a scorecard that ranks I.
polyantha among the most threatened
species in the State based on number of
plants, quality of the plants and habitat,
threats, and adequacy of protection
(CNHP and TNC 2008, p. 102).
Ipomopsis polyantha is in the
Polemoniaceae (phlox) family and was
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originally described by Rydberg (1904,
p. 634) as Gilia polyantha. Grant (1956,
p. 353) moved the species into the genus
Ipomopsis. Two varieties,G. polyantha
var. brachysiphon and G. polyantha var.
whitingii, were recognized by Kearney
and Peebles (1943, p. 59). Currently
available information indicates that I.
polyantha is a distinct species (Porter
and Johnson 2000; Porter et al. 2003 in
Anderson 2004, p. 11). It is treated as
such in the PLANTS database (United
States Department of Agriculture
(USDA)/Natural Resource Conservation
Service (NRCS) 2003), and in the
Integrated Taxonomic Information
System (2001).
Ipomopsis polyantha is an herbaceous
biennial 12 to 24 inches (in.) (30 to 60
centimeters (cm)) tall, branched from
near the base above the basal rosette of
leaves. Deeply divided leaves with
linear segments are scattered up the
stem. Stems and flower clusters are
covered with glandular hairs. Flower
clusters are along the stem in the axils
of the leaves as well as at the top of the
stem. The white flowers are 0.4 in. (1
cm) long, with short corolla tubes 0.18
to 0.26 in. (0.45 to 0.65 cm) long, and
flaring corolla lobes flecked with purple
dots (Anderson 1988, p. 3). These dots
are often so dense that they give the
flower a pinkish or purplish hue. The
stamens extend noticeably beyond the
flower tube, and the pollen is blue
(Grant 1956, p. 353), changing to yellow
as it matures (Collins 1995, p. 34). Firstyear plants form basal rosettes of leaves.
These rosettes produce flowering stalks
during the next growing season, or they
may persist for more than 1 year
without flowering, until they get enough
moisture to flower Plants produce
abundant fruits and seeds, but have no
known mechanism for long distance
dispersal (Collins 1995, pp. 111–112).
After seeds are mature, the plants dry
up and die.
Pollination by bees is the most
common means of reproduction for
Ipomopsis polyantha, and the primary
pollinators are a honey bee (Apis
mellifera), metallic green bee
(Augochlorella spp.), bumble bee
(Bombus spp.), and digger bee
(Anthophora spp.) (Collins 1995, pp. 7172).
Ipomopsis polyantha is limited to
Pagosa-Winifred soils derived from
Mancos Shale. The soil pH is nearly
neutral to slightly alkaline (6.6 to 8.4).
The elevation range is 6,800 to 7,300
feet (ft) (2,072 to 2,225 meters (m)).
Plants occur in discontinuous colonies
as a pioneer species on open shale or as
a climax species along the edge of
ponderosa pine/juniper/oak forested
areas. In 1988, Anderson (p. 7) reported
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finding the highest densities under
ponderosa pine forests with montane
grassland understory. Now the species
is found mostly on sites that are
infrequently disturbed by grazing, such
as road rights-of-way (ROWs) that are
fenced from grazing (as opposed to open
range), lightly grazed pastures, and
undeveloped lots (Anderson 2004, p.
20).
Habitat for the species is
characterized as suitable, potential, or
unsuitable. Suitable habitat has the
attributes of soil and elevation described
above, and we further separate it into
occupied habitat where the plants have
been observed and unoccupied habitat
where soil and elevation are suitable but
no plants have been observed or no
surveys have been conducted. Potential
habitat is identified remotely, using
aerial photographs, soil maps, and other
available information, to build a model
of habitat that may support I. polyantha.
The model has not been ground-truthed
in the field. Unsuitable habitat is found
at elevations and on soils that do not fit
the profile for the species, or habitat that
has been altered by development,
paving, or other human activities so that
the plants are prevented from growing
there.
There are two known occurrences of
Ipomopsis polyantha. Between its
description by C.F. Baker in 1899, and
inventories in 1985, I. polyantha was
only known from along U.S. Route 84
(US 84) in the vicinity of Pagosa
Springs, Colorado (Anderson 1988, pp.
1–2, 15–16). The Pagosa Springs
occurrence is still the largest occurrence
of the species. In 1985, an additional
occurrence was found about 10 mi (16
km) west of town along U.S. Route 160
(US 160) in a rural area called Dyke
(Anderson 1988, pp. 1–2). In 2002,
another occurrence was documented in
a rural area called Mill Creek, about 1.2
mi (1.9 km) east of Pagosa Springs
(Anderson 2004, p. 13; CNHP 2008a, ID
228). The Mill Creek area is now
included in the Pagosa Springs
occurrence, in accordance with
NatureServe criteria: occurrences are
separated by at least 0.62 mi (1 km) of
unsuitable habitat or 1.24 mi (2 km) of
suitable habitat (NatureServe 2004, p.
1). The two known occurrences are
within about 13 mi (21 km) of each
other, and collectively occupy
approximately about 50 ac (20 ha) of
habitat within a range that includes
about 4 square mi (10.4 square km).
Table 1 summarizes known occupied
habitat (50 ac (20 ha)) combined with
suitable habitat not verified as occupied
within the two I. polyantha occurrences
(total 234 ac (94 ha)).
TABLE 1. OCCUPIED AND UNSURVEYED SUITABLE HABITAT FOR Ipomopsis polyantha (CNAP 2007, PP. 1–5; LYON 2005,
P. 1; LYON 2006A, P. 1–2; MAYO 2008A, P. 1; CNHP 2008A, ID 228)
Occurrence
Land Ownership
Pagosa Springs including Mill Creek
ac (ha)
State ROW
Flowering
Plants
Rosettes
19 (7.7)
3,029
3,083
County ROW
3 (1.2)
126
NA
Archuleta County
1 (0.4)
280
NA
Town of Pagosa Springs
1 (0.4)
3
15
184 (74)
Unsurveyed
NA
3 (1.2)
156,126
173,189
211 (85)
159,564
176,287
State ROW
3 (1.2)
141
176
BLM
20 (8)
88
164
23 (9)
229
340
234 (94)
159,793
176,627
Private (suitable)
Private Corporation
Subtotals
Dyke
Subtotals
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Totals
All
The total occupied and surveyed
habitat for Ipomopsis polyantha covers
about 50 ac (20 ha). Suitable habitat for
the species has been identified on about
211 acres (ac) (85 hectares (ha)) on the
east side of town, and on about 23 ac (9
ha) approximately 10 miles (mi) (16
kilometers (km)) west of town.
Approximately 9 percent of the suitable
habitat is on federally owned Bureau of
Land Management (BLM) land, 12
percent on State and County highway
ROWs, 78 percent on private lands, and
less than 1 percent on Pagosa Springs
Town park land and county land
(Colorado Natural Areas Program
(CNAP) 2007). An estimated 184 ac (74
ha), or 79 percent, of the suitable habitat
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exists on private residential and
agricultural land where plants have
been observed from a distance, but
surveys have not been conducted.
Without access to these private lands,
the extent of occupancy cannot be
assessed.
The historical range of Ipomopsis
polyantha is unknown, but likely
included a much broader area than the
currently occupied habitat. Many
surveys of potential habitat in the
Pagosa Springs area have been
conducted over the years with negative
results. Potential habitat on about 2,018
ac (817 ha) within the known range has
not been surveyed due to lack of access
to private lands. All of this potential
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habitat is close to or surrounded by
suitable habitat, and is currently
proposed for development, including:
Blue Sky Village 96 ac (39 ha); Blue Sky
Ranch 1,362 ac (551 ha); and Fairway
560 ac (227 ha) (see Threat Factor A
below).
None of the potential habitat
identified to date extends beyond the
approximately 4-square-mi (10.4-squarekm) occupied range of the species.
Reports of this species occurring in
Arizona and New Mexico by the
PLANTS National Database and State
floras actually pertain to the two species
that were formerly treated as varieties of
Ipomopsis polyantha (Anderson 2004,
pp. 11, 15).
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The Pagosa Springs occurrence of
Ipomopsis polyantha is southeast of the
town along both sides of US 84.
Occupied habitat extends southward on
the highway ROW for 3 mi (4.8 km)
from the intersection with US 160, and
on private lands on both sides of the
highway within 0.25 to 1.2 mi (0.4 to 1.9
km). In 1985, the estimated number of
flowering plants in this occurrence was
2,000 (Anderson 1988, p. 8). During
2005-2006, 3,029 flowering plants and
3,083 rosettes were counted on about 19
ac (7.7 ha) of highway ROW and
immediately adjacent private lands
(CNAP 2007, pp. 1–5; Lyon 2005, p. 1;
Lyon 2006a, pp. 1–2). In 2005, an
additional 156,126 plants and 173,189
rosettes were found on a 3-ac (1.2-ha)
private land site, which was a high
density of plants on a site where no
plants had been observed in previous
years (Lyon 2005, pp. 3–4; Lyon 2007b,
p. 1). The plants were found on a
hillside of Mancos Shale about 7 years
after it was bladed, and are still growing
there because the ground has not been
disturbed during the growing season
(Lyon 2007b, p. 2). I. polyantha quickly
colonizes unvegetated Mancos Shale
near a seed source. The number of
flowering plants that appear in
subsequent years depends on seed
production and the survival of rosettes
that are not outcompeted by other
species or destroyed during ground
disturbance.
In addition to the surveyed plants and
rosettes, many flowering Ipomopsis
polyantha plants have been seen, but
not counted, on private residential/
agricultural parcels along US 84 (Lyon
2006a, p. 1). An estimated 184 ac (74 ha)
of unsurveyed suitable habitat on
private lands exist within the Pagosa
Springs occurrence.
The Dyke occurrence includes 0.5 mi
(0.8 km) of highway ROW on both sides
of US 160, adjacent private land, and
about half of a 40-ac (16-ha) BLM parcel
on the north side. On both of the ROWs
and adjacent pastures, more than 500
flowering plants were estimated in 1985
(Anderson 1988, p. 10). In 1991, about
250 plants were counted in unused
pasture on the south side, but no plants
were found in subsequent years after
cattle were returned to the pasture
(Collins 1995, pp. 111–112). The
number of flowering plants and rosettes
on the US 160 ROW have fluctuated
each year between 2005 and 2008. On
the north side ROW, the number of
flowering plants and rosettes declined
by 80 percent over the 4 years, to 9 and
8 respectively. On the south side ROW,
flowering plants increased 176 percent
(to 141 plants), and rosettes declined 9
percent (to 179 rosettes) (Mayo 2008a, p.
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1). The approximately 20-ac (8-ha) BLM
parcel is the only federally managed
habitat for the species. There, in 2006,
88 flowering plants and 164 rosettes
were found in clearings among
ponderosa pine and shrubs (CNAP 2007,
p. 2).
In addition to these extant
occurrences, about 13 plants and 18
rosettes were found on a roadside in a
residential area north of Pagosa Springs
in 2005. We do not consider this
occurrence as extant, because no plants
have been found there since 2005.
Surveys of roadsides and private lands
in this vicinity, and on additional
potential habitat north of town, have not
detected any individuals of the species
(Lyon 2005, p. 3).
In 2004, the total estimate of
flowering plants throughout the entire
range of the species was 2,246 to 10,526
(Anderson 2004, p. 40). Plant surveys
from 2005 to 2007 document dramatic
increases in the number of flowering
individuals and rosettes within the
Pagosa Springs occurrence at two sites
on private land and on the US 84 ROW
(CNAP 2007, pp. 1–2). Currently, the
total estimate of flowering plants is
159,793 (see Table 1 above). This
increase is primarily attributed to the
plants surveyed in 2005 and 2006 on the
3-ac (1.2-ha) private land site in the
Pagosa Springs occurrence. The rapid
appearance of such a dense patch of
plants illustrates the specie’s ability to
colonize barren Mancos Shale soil, and
demonstrates the reproductive success
of the species; however, the sites where
they grow are vulnerable to habitat
destruction. The trend in the species’
status since 1988 is one of fluctuating
population size that is typical of
biennial species, combined with the loss
of some plants due to development.
Summary of Factors Affecting
Ipomopsis polyantha
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Ipomopsis polyantha is threatened
with destruction of plants and habitat
due to commercial, residential, and
agricultural property development, and
associated new utility installations and
access roads. We have documented
recent losses of habitat and individuals
at six sites within the Pagosa Springs
occurrence of the species, as described
in more detail below.
Within the Pagosa Springs
occurrence, a residential and
agricultural development of about a
dozen 35-ac (14-ha) parcels was built
prior to 2005 on occupied habitat east
of US 84 (Archuleta County Assessor
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2008, p. 1). In 2005, when most
residences were new, about 782
flowering plants were counted in
meadows and along the fences and
access roads (Lyon 2005, pp. 1–2). By
2008, an increased number of horses
were pastured in the meadows,
roadsides and driveways were graded or
widened, and few plants could be found
as a result (Mayo 2008b, p. 1). This
information indicates that Ipomopsis
polyantha plants are vulnerable to
grazing and road improvements, and
habitat can be modified to exclude
plants in as few as 3 years. In 2006, at
another location along US 84, a private
landowner mowed several hundred feet
of occupied habitat on the highway
ROW (Lyon 2006a, p. 1). No plants were
found at this site from 2006 to 2008,
indicating that mowing destroys plants
and halts reproduction. In 2005, dense
patches of flowering plants were noted,
from across the fence, in a privately
owned meadow along US 84. In 2007,
a new home was built, and the meadow
was mowed; no plants could be seen at
the same site in 2008 (Mayo 2008b, p.
2), again indicating that mowing
destroys plants and inhibits
reproduction. During 2005 and 2006, a
sewer line installation on the US 84
ROW resulted in the loss of about 498
plants and 541 rosettes, and
modification of about 1,473 ft (449 m)
of roadside habitat (Mayo 2008c, p. 8).
The Colorado Department of
Transportation (CDOT) and Archuleta
County consulted with us, and agreed
on avoidance measures for this project,
but contractors failed to follow the
protocol (Mayo 2008c, pp. 1–4). In 2008,
only a few flowering plants and rosettes
were found at this site; all of the plants
were in one spot near plants on an
adjacent property not disturbed by the
sewer line project (Mayo 2008c, p. 8).
This incident demonstrates that I.
polyantha cannot quickly recover from
soil disturbance.
Utility installations and construction
activities can eliminate habitat and
destroy Ipomopsis polyantha. As a
result of careful planning, in 2007,
power line maintenance was completed
within occupied habitat in the Pagosa
Springs occurrence with negligible
damage to adult plants. Rosettes in the
path of maintenance actions were
transplanted to suitable habitat in the
town park. The 278 transplants survived
the winter and produced about 27
flowering plants. However, no surviving
rosettes could be relocated in the fall
(Coe 2007, pp. 2–3). A second attempt
at transplanting rosettes to save them
from destruction during utility
installations also has not been effective
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in producing new rosettes in the third
year (Brinton 2007, pers. comm.).
Unless effective methods are developed,
most plants that cannot be avoided
during utility installations and
construction activities are unlikely to
survive and reproduce. Whether the
species can survive translocation under
other circumstances remains uncertain.
Primary land use within the range of
Ipomopsis polyantha has historically
been agricultural, with homes and
horses or cattle on parcels of 35 ac (14
ha) or more. Several small businesses
now occur along US 84 within the
Pagosa Springs occurrence. The
intersection of US 160 and US 84 is
zoned by the Town of Pagosa Springs
for businesses, and commercially zoned
land is currently available for
development. The County is also
considering sites in this area for new
municipal buildings; one of the sites
under consideration contains the
highest density of I. polyantha
occurrence. These current and potential
conversions of agricultural lands to
residential and commercial
development are incompatible with
conservation of I. polyantha in the long
term because they cause direct mortality
and permanent loss of habitat, whereas
habitat modified by grazing may be
recovered by changes in management.
The privately owned property across
the entire range of Ipomopsis polyantha
was scheduled for development in the
Archuleta County and Town of Pagosa
Springs Community Plan (2000). In this
plan, all areas occupied by I. polyantha
on private land outside of the Town
limits are planned for low (35 ac (14
ha)), medium (3 to 35 ac (1.2 to 14 ha)),
or high (2 to 5 ac (0.81 to 2 ha)) density
housing. Residential development is
increasing rapidly in the County. The
population of Archuleta County was
5,000 in 1990; the projection is 15,000
people by 2010 and 20,000 by 2020
(Archuleta County and Town of Pagosa
Springs 2000, pp. 5–7). Based on the
rate of current and proposed
development over the entire range of the
species, 85 percent of occupied and
suitable habitat and all potential habitat
could be modified or destroyed within
5 to 10 years, putting the species at risk
of extinction.
The County plan for agricultural and
large-lot residential development along
US 84 became obsolete in 2008, with the
Pagosa Town Council’s preliminary
approval of a 96-ac (39-ha) Blue Sky
Village annexation (Aragon 2008a, pp.
1–2). The proposed development plan is
for a mixed commercial and high-to-low
density residential village (Hudson
2008, p. 1). The 96-ac (39-ha) parcel is
adjacent to the highest density of
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Ipomopsis polyantha plants, and
includes about 2,562 ft (781 m) of
potential habitat on US 84 frontage at
the center of the species’ distribution
(Archuleta County Assessor 2008, p. 1).
Occupied habitat also borders the
southern edge of the property. Reducing
habitat available to the Pagosa Springs
occurrence of I. polyantha will limit its
ability to disperse and repopulate after
impacts.
In addition to the loss of potential
habitat on private land for the plants,
the proposed annexation will require
access roads, utility installations, and
acceleration and deceleration lanes
along the highway ROW. Plants and
habitat will likely be destroyed by this
infrastructure construction. The Blue
Sky Village development will
significantly reduce the amount of
potential habitat within the species’
range. Location of the development
between the highest density of plants
and the rest of the Pagosa Springs
occurrence on the east side of US 84
will further fragment the habitat that has
already been impacted by commercial,
residential, and agricultural land uses.
The Blue Sky Ranch development of
1,362 ac (551 ha), plus 2,819 ft (859 m)
of US 84 frontage, is another annexation
being considered within potential
Ipomopsis polyantha habitat. This
project would include single and multifamily residential housing, a hotel and
conference center, a golf course with
clubhouse, and an equestrian center
with riding trails and a multi-use arena
(Aragon 2008b, p. 2).
A development of 560 ac (227 ha),
including about 1 mi (1.6 km) of
frontage along the west side of US 84,
also is being considered for annexation
within potential habitat that has not
been surveyed for plants (Aragon 2008a,
p. 2; Archuleta County Assessor 2008, p.
1).
The above three development
proposals within the Pagosa Springs
occurrence cover a total of 2,018 ac (817
ha) of potential habitat for the plants
that have not been surveyed due to
restricted access. The proposed
developments include frontage along
the US highway 84 ROW that currently
provides 34 percent of the total habitat
occupied by the plants (Archuleta
County 2008, p. 1). Plants and habitat
on this ROW are likely to be disturbed
or removed by construction of new
access roads, acceleration lanes, and
utilities to accommodate the
development.
The Archuleta County and Town of
Pagosa Springs revised 2004 Trails Plan
(2004, p. 18) calls for an 8-ft (2.4 m)
wide, 2.5-mi (4 km) long, paved bike
path on the highway ROW from US 160
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south along US 84 in occupied
Ipomopsis polyantha habitat. This
route, prioritized for completion as soon
as funding is available, would eliminate
about 50 percent of the occupied habitat
on the highway ROW and 80 percent of
the total occupied area in the Pagosa
Springs occurrence (see Table 1 above).
Another planned paved bike trail,
parallel to US 160 and through the Dyke
occurrence of I. polyantha, is on the low
priority list in the Trails Plan (Archuleta
County and Town of Pagosa Springs
2004, p. 28). Development of this bike
trail would eliminate the portion of the
Dyke occurrence located on the south
side of the highway where the trail
would be located.
Distribution of Ipomopsis polyantha
on highway ROWs makes this species
susceptible to threats associated with
highway activities and maintenance.
Exotic grasses planted by CDOT along
roadsides dominate the ROW between
pavement and ditch, limiting most I.
polyantha plants to the ROW bank
between ditch and fence. This limitation
to the species’ habitat along roadsides is
significant because so little habitat
exists elsewhere for the species. I.
polyantha plants growing among
thistles were killed by herbicide within
the highway ROW along US 84 in 2004,
when the thistles were treated with
herbicide (Anderson 2004, p. 36). Since
that time, Archuleta County has
discontinued broadcast herbicide use
and mowing on ROWs within the
species’ range. However, the planted
exotic grasses continue to limit the
species’ habitat.
Highway ROWs provide about 50
percent of the occupied habitat for
Ipomopsis polyantha. All highway ROW
habitat is at risk of disturbance by
construction of new access roads or
acceleration lanes, bike paths, and
utilities installation or maintenance.
Such construction results in direct loss
of I. polyantha individuals or reduced
suitability of its habitat by altering the
soil characteristics or displacing the
seed bank (Anderson 2004, p. 36).
We determined that the present and
threatened destruction, modification,
and fragmentation of Ipomopsis
polyantha habitat from ongoing
commercial and residential
development, associated new utility
installations, construction of new access
roads and bike paths, competition from
introduced roadside grasses and other
impacts associated with proximity to
highways are significant and imminent
threats to the species throughout its
range. At this time, the species
primarily persists on highway ROWs
and private lands scheduled for
development. Development planned for
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the next 5 to 10 years will likely: (1)
Impact over 2,000 ac (809 ha) of
potential habitat; (2) potentially
eliminate 167 of the 214 ac (68 of 87 ha)
of existing occupied and suitable habitat
on private lands; and (3) potentially
eliminate about 34 percent of the
highway ROW (occupied) habitat.
Combined, these impacts would relegate
the species primarily to small,
fragmented portions of highway ROWs
and a few, small, lightly-used private
pastures putting the species in danger of
extinction.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Activities resulting in overutilization
of Ipomopsis polyantha plants for
commercial, recreational, scientific, or
educational purposes are not known to
exist. Therefore, this factor is not
addressed in this proposal.
C. Disease or Predation
Disease
Disease is not known to affect
Ipomopsis polyantha. Therefore, disease
is not addressed in this proposal.
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Predation
This species is threatened by
destruction of flowering plants, rosettes,
and seeds due to concentrated livestock
disturbance and some herbivory.
Observations of the ‘‘fence line effect’’—
healthy plants outside the fence and
impacted plants inside the fence—at
several locations on private land used
for cattle and horse grazing indicate that
Ipomopsis polyantha does not tolerate
intensive livestock grazing (Anderson
2004, p. 30). For example, grazing by
horses at a residential/agricultural
development within the Pagosa Springs
occurrence in 2005 resulted in few I.
polyantha plants 3 years later (Mayo
2008b, p. 1). Over-the-fence
observations from seven locations
(pastures) in 2009 found few or no
plants in the three heavily grazed
pastures and numerous plants in the
adjacent pastures with light or no
grazing (Glenne 2010, pp. 1-3). We have
no data to indicate whether the plant
destruction results from herbivory or
from trampling. I. polyantha is not
found in heavily grazed pastures, but
occurrences have been observed in
lightly grazed horse pastures and
abandoned pastures (CNAP 2007, p. 6).
Plants could possibly recolonize a
pasture if livestock numbers were
reduced sufficiently and the seed bank
was still viable, or if there was a seed
source nearby, such as on the ungrazed
side of a fence. Indications are that the
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species may be compatible with light
grazing, but the level of impact and the
threshold of species’ tolerance have not
been studied. Evidence indicates that
few plants persist in areas of continual
grazing (Collins 1995, pp. 107, 111,
112). We determined that destruction of
flowering plants, rosettes, and seeds due
to heavy livestock use is a significant
and imminent threat to I. polyantha.
D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
City and county ordinances have the
potential to affect Ipomopsis polyantha
and its habitats. Zoning that protects
open space can retain suitable habitat,
and zoning that allows commercial
development can destroy or fragment
habitat. We know of no city or county
ordinances that provide for protection
or conservation of I. polyantha or its
habitat. Archuleta County road
maintenance crews refrain from mowing
or broadcast spraying ROWs within the
range of Ipomopsis polyantha
voluntarily, that is, without the mandate
or support of regulations. However,
there is no law, regulation, or policy
requiring them to do so.
New annexation of 2,018 ac (817 ha)
into the Town of Pagosa Springs will
change land use from 35-ac (14-ha)
agricultural parcels to commercial and
small lot residential, with anticipated
adverse impacts to the Pagosa Springs
occurrence of I. polyantha. This land
use conversion, as described in Factor A
above, is the most significant threat to
the species, because development
planned for the next 5 to 10 years will
likely impact all known potential
habitat and 17 of 25 ROW acres (6.9 of
10 ha), and relegate the species to
private residential areas and small,
fragmented portions of highway ROWs.
State Laws and Regulations
No State regulations protect rare plant
species in Colorado. Ipomopsis
polyantha is classified by CNHP as a G1
and S1 species, which means it is
critically imperiled across its entire
range and within the State of Colorado
(CNHP 2006a, p. 1). The CDOT has
drafted best management practices for
ROWs within I. polyantha habitat in
collaboration with the Service (Peterson
2008, p. 1). In 2006, voluntary measures
to minimize impacts to plants from a
sewer line installation along US 84 were
recommended by CDOT, but not
implemented by the contractors (Mayo
2008c, pp. 1–4).
Federal Laws and Regulations
Ipomopsis polyantha is on the
sensitive species lists for the U.S. Forest
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Service (USFS) and the BLM (USFS
2009, p. 6; BLM 2008b, p. 47). Occupied
habitat has not been found on USFS
land. In 2006, we learned that the Dyke
occurrence extends onto 20 ac (8 ha) of
BLM land (Lyon 2007b, pp. 3, 12, 13);
88 plants and 164 rosettes were found
there in 2007 (CNAP 2007, p. 2). This
BLM parcel was withdrawn from a
proposed land exchange so that the
plant habitat would remain under
Federal management (Brinton 2009,
pers. comm.; Lyon 2007b, p. 3). The
species has no Federal regulatory
protection for approximately 91 percent
of the total known occupied and
suitable habitat. It occurs mostly on
State and private land (see Table 1
above), and development of these areas
will likely require no Federal permit or
other authorization. Therefore, projects
that affect it are usually not analyzed
under the National Environmental
Policy Act (NEPA)(42 U.S.C. 4321 et
seq.).
We determined that the inadequacy of
existing regulatory mechanisms is a
significant and imminent threat to
Ipomopsis polyantha, because 91
percent of the known range of the
species is on State and private lands
that carry no protective regulations to
ameliorate activities that will impact the
species.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
The adaptation of Ipomopsis
polyantha to Pagosa-Winifred soils
derived from Mancos Shale limits it to
about 4 square mi (10.4 square km)
within a 13-mi (21-km) range of
fragmented habitat on outcrops of
Mancos Shale. The species has specific
physiological requirements for
germination and growth that may
prevent its spread to other locations
(Anderson 2004, pp. 23–24). In
greenhouse trials, seeds will germinate
and grow on other soils, but they grow
much faster on Mancos Shale soils
(Collins 1995, p. 114). Faster growth
may give I. polyantha a competitive
advantage on relatively barren Mancos
shale that it lacks on other soils where
its smaller seedlings have more
competition from other plants for
nutrients and water. The species
produces more seed when it is crosspollinated (Anderson 2004, p. 23);
therefore, existing and foreseeable
fragmentation of habitat may cause gene
flow to be obstructed. Pollinatormediated pollen dispersal is typically
limited to the foraging distances of
pollinators, and no bee species is
expected to travel more than 1 mi (1.6
km) to forage (Tepedino 2009, p. 11).
Thus, it is likely that the occurrence of
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about 191 plants west of Pagosa Springs
is genetically isolated from the other
occurrence several miles (kilometers)
away. Spatially isolated plant
populations are at higher risk of
extinction due to inbreeding depression,
loss of genetic heterogeneity, and
reduced dispersal rates (Silvertown and
Charlesworth 2001, p. 185).
Ipomopsis polyantha shows great
differences in plant numbers from year
to year, probably because the plants are
biennial and grow from seed. This trait
makes them more vulnerable than
perennials to changes in environment,
including timing and amount of
moisture, and length of time since
disturbance. With increased time after
disturbance, competition from other
plants, both native and nonnative,
increases (CNAP 2008a, p. 4). As a
biennial species, I. polyantha also may
be vulnerable to prolonged drought.
During drought years, seeds may not
germinate and plants may remain as
rosettes without flowering or producing
a new crop of seeds.
Climate change could potentially
impact Ipomopsis polyantha. Localized
projections indicate the southwest may
experience the greatest temperature
increase of any area in the lower 48
States (IPCC 2007, p. 30). A 10- to 30percent decrease in precipitation in
mid-latitude western North America is
projected by the year 2050, based on an
ensemble of 12 climate models (Milly et
al. 2005, p. 1). Climate modeling at this
time has not been refined to the level
that we can predict the amount of
temperature and precipitation change
within the limited range of I. polyantha.
Therefore, this analysis is speculative
based on what the data indicate at this
time. When plant populations are
impacted by reduced reproduction
during drought years, they may require
several years to recover. Climate change
may exacerbate the frequency and
intensity of droughts in this area and
result in reduced species’ viability as
the dry years become more common. As
described above, I. polyantha is
sensitive to the timing and amount of
moisture due to its biennial life history.
Thus, if climate change results in local
drying, the species could experience a
reduction in its reproductive output.
Recent analyses of long-term data sets
show accelerating rates of climate
change over the past two or three
decades, indicating that the extension of
species’ geographic range boundaries
towards the poles or to higher elevations
by progressive establishment of new
local occurences will become
increasingly apparent in the short term
(Hughes 2000, p. 60). The limited
geographic range of the Mancos Shale
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substrate that underlies the entire
Ipomopsis polyantha habitat likely
limits the ability of the species to adapt
by shifting occurrences in response to
climatic conditions.
We determined that the natural and
human-caused factors of specific soil
and germination requirements,
fragmented habitat, effects of drought
and climate change, and lack of proven
methods for propagation present an
imminent and moderate degree of threat
to Ipomopsis polyantha across the entire
range of the species.
Background—Penstemon debilis
Previous Federal Actions
We first included Penstemon debilis
as a category 2 candidate species in the
February 21, 1990, Review of Plant Taxa
for Listing as Endangered or Threatened
Species (55 FR 6184). Category 2
candidate species were defined as
‘‘[t]axa for which there is some evidence
of vulnerability, but for which there are
not enough data to support listing
proposals at this time’’ (55 FR 6185,
February 21, 1990). In 1996, we
abandoned the use of numerical
category designations and changed the
status of P. debilis to a candidate under
the current definition. We published
four CNOR lists between 1996 and 2004,
and P. debilis remained a candidate
species with a LPN of 5 on each (62 FR
49398, September 19, 1997; 64 FR
57534, October 25, 1999; 66 FR 54808,
October 30, 2001; 67 FR 40657, June 13,
2002). A LPN of 5 is assigned to species
with non-imminent threats of a high
magnitude.
On March 15, 2004, the Center for
Native Ecosystems (CNE) and the
Colorado Native Plant Society
petitioned us to list Penstemon debilis
(CNE 2004a, p. 1). We considered the
information provided in their petition
when we prepared the 2004 CNOR. In
the 2004 CNOR, P. debilis remained a
candidate species with a listing priority
of 5 (69 FR 24876, May 4, 2004).
On May 11, 2004, we received a
petition from the Center for Biological
Diversity (CBD) to list 225 species we
previously had identified as candidates
for listing, including Penstemon debilis
(CBD 2004, p. 6). Under requirements in
section 4(b)(3)(B) of the Act, the CNOR
and Notice of Findings on Resubmitted
Petitions published on May 11, 2005 (70
FR 24870), raised the LPN of P. debilis
from 5 to 2 but also included a finding
that the immediate issuance of a
proposed listing rule and the timely
promulgation of a final rule for each of
225 petitioned species, including P.
debilis, was warranted but precluded by
higher priority listing actions, and that
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expeditious progress was being made to
add qualified species to the Lists (70 FR
24870, May 11, 2005).
On November 15, 2004, the CNE
issued a 60–day notice of intent to sue
for violation of section (4)(b)(3)(A) of the
Act with respect to the petition to list
Penstemon debilis (CNE 2004b, pp. 1–
2). On January 25, 2005, Biodiversity
Conservation Alliance and seven other
entities filed an amended complaint
regarding our failure to list P. debilis
and five other species. As part of a
settlement agreement, plaintiffs
withdrew their lawsuit regarding P.
debilis.
In the 2005 CNOR (70 FR 24870), as
stated above, the listing priority number
for Penstemon debilis was changed from
5 to 2 based on an increase in the
intensity of energy exploration along the
Roan Plateau escarpment, making the
threats to the species imminent (70 FR
24870, May 11, 2005). A listing priority
of 2 represents threats that are both
imminent and high in magnitude. CNOR
lists published in 2006 and 2007
maintained P. debilis as a candidate
species with a listing priority of 2 (71
FR 53756, September 12, 2006; 72 FR
69034, December 6, 2007).
In each assessment since its
recognition as a candidate species in
1996, we determined that publication of
a proposed rule to list the species was
precluded by our work on higher
priority listing actions. However, in
2008, we received funding to initiate the
proposal to list Penstemon debilis.
Species Information
Penstemon debilis is a rare plant,
endemic to oil shale outcrops on the
Roan Plateau escarpment in Garfield
County, Colorado. This species is
known by the common names Parachute
beardtongue and Parachute penstemon.
P. debilis is classified by the CNHP as
a G1 and S1 species, which means it is
critically imperiled across its entire
range and within the State of Colorado
(CNHP 2008b, p. 14). The total
estimated number of known plants is
approximately 4,000 individuals (CNHP
2006b, p. 1; CNHP 2009a, p. 1; CNHP
2009b, p. 1; CNHP 2009c, p. 1; CNHP
2009d, p. 2). Approximately 82 percent
of the known plants are on private land
owned by a natural gas and oil shale
production company. Most of the
remaining 18 percent occur in one
occurrence on BLM land that was
recently leased under a new Resource
Management Plan (RMP) amendment
(BLM 2008a, Record of Decision (ROD)
p. 2). In recent years, energy
development has increased in this area
on both private and Federal lands.
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Traditionally Penstemon has been
included in the Scrophulariaceae
(figwort family). Phylogenetic studies
based on DNA sequences of taxa in this
and related plant families over the last
10 years have necessitated realignment
of several genera in these groups. Apart
from a nomenclatural discrepancy,
Penstemon has been shown to be a part
of the Plantaginaceae (plantain) family,
since 2001. The chronology and
summary of the placement of
Penstemon in the Plantaginaceae is
presented by Oxelman et al. (2005, p.
415). We recognize this placement and
will make the appropriate attribution in
the proposed amendments to 50 CFR
17.12(h) at the end of this document.
The text will include the family name
as Plantaginaceae.
Penstemon debilis was discovered in
1986, and was first described by O’Kane
and Anderson in 1987 (pp. 412–416. No
challenges have been made to the
taxonomy as first put forward by the
authors. Penstemon debilis is a matforming perennial herb with thick,
succulent, bluish leaves, each about 0.8
in. (2 cm) long and 0.4 in. (1 cm) wide.
Plants produce shoots that run along
underground, forming what appear as
new plants at short distances away.
Individual P. debilis plants are able to
survive on the steep, unstable, shale
slopes by responding with stem
elongation as leaves are buried by the
shifting talus. Buried stems
progressively elongate down slope from
the initial point of rooting to a surface
sufficiently stable to allow the
development of a tuft of leaves and
flowers (O’Kane and Anderson 1987,
pp. 414–415). Flowers are funnelshaped, are white to pale lavender, and
flower during June and July. P. debilis
plants produce a low number of seeds,
are primarily outcrossers, and have
many different pollinators that vary
between occurrences (McMullen 1998,
p. 26). None of the pollinators are
specialists to P. debilis, nor are any of
them rare (McMullen 1998, p. 31). We
know little about the lifecycle of
Penstemon debilis with regard to
generational timetables.
Penstemon debilis seems to be at least
somewhat adapted to disturbance. Each
of the known occurrences of the species
contains high levels of physical
disturbance (McMullen 1998, p. 81).
Many of the characteristics that are most
similar among sites promote continual
disturbance: steep slopes, unstable shale
channer surface layers, and no surface
soil (McMullen 1998, p. 82). In fact, two
of the largest P. debilis occurrences, are
on recent mine talus slopes where
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anthropogenic disturbance was very
high as recently as 1994 (McMullen
1998, p. 82). One occurrence was
recorded to have several hundred
individuals in 1994, but no individuals
can be found at this site today
(McMullen 1998, p. 82). This may be a
result of a reduction in the disturbance
levels through successional processes
such as soil development and increased
vegetative cover (McMullen 1998, p.
82). Penstemon debilis may be
considered a pioneer species that
disperses to recent disturbances,
flourishes, and goes locally extinct if
soil conditions become stable
(McMullen 1998, p. 82).
Penstemon debilis grows on steep, oil
shale outcrop slopes of white shale talus
at 8,000 to 9,000 ft (2,400 to 2,700 m)
in elevation on the southern escarpment
of the Roan Plateau above the Colorado
River west of the town of Parachute,
Colorado. The Roan Plateau falls into
the geologic structural basin known as
the Piceance Basin. Average annual
precipitation at Parachute, Colorado, is
12.75 in. (32.4 cm) (IDcide 2009, p. 1).
P. debilis is found only on the Parachute
Creek Member of the Green River
Formation. P. debilis is often found
growing with other species endemic to
the Green River formation, including
Astragalus lutosus (dragon milkvetch),
Festuca dasyclada (Utah fescue),
Mentzelia argillosa (Arapien stickleaf),
and Thalictrum heliophilum (sun-loving
meadowrue), as well as several nonendemics (O’Kane & Anderson 1987, p.
415).
The historical range and distribution
for this species is unknown. All of the
currently known occurrences occur on
about 56 ac (23 ha) in Garfield County.
The Green River geologic formation to
which the plant is restricted is the major
source of oil shale in the United States.
Although this formation is underground
throughout most of the Piceance Basin,
it is exposed on much of the southern
face of the Roan Plateau. The total area
of the plant’s geographic range is about
2 mi (3 km) wide and 8 mi (13 km) long.
Prior to 1997, two occurrences of P.
debilis were known. In 1997, the CNHP
used existing habitat and distribution
information, along with soils, geology,
and aerial photographs, to select target
survey areas. The ensuing survey
resulted in the discovery of two new
occurrences (Spackman et al. 1997, p.
6). Two other occurrences were first
recorded by BLM in 1997 and 2005 at
oil shale mine sites (CNHP 2009a, p. 1;
CNHP 2009d, p. 1). Another occurrence
of approximately 12 plants was reported
in June 2009 (Graham 2009a, pp. 1–2).
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It is likely that unknown occurrences
exist, because many areas are simply
inaccessible to surveyors due to steep
terrain or private land ownership or
both.
Penstemon debilis occurs at seven
known occurrences, four of which are
rated by CNHP as having ‘‘good to
excellent’’ estimated viability based on
population size, individual plant sizes,
and site ecology (CNHP 2006b, p. 1;
CNHP 2009a, p. 1; CNHP 2009b, p. 1;
CNHP 2009c, p. 1; CNHP 2009d, p. 2)
(see Table 2 below). The largest
occurrence (Mount Callahan Natural
Area) of 2,100 to 2,240 plants grows on
lands owned by an energy development
company (CNAP 2006, p. 1). The Mount
Callahan Ridge occurrence, with an
estimated 650 plants, grows on lands
owned by the same energy development
company (CNAP 2006, pp. 1–2). The
Anvil Points Road occurrence grows on
lands administered by the BLM and has
an estimated 700 plants (CNHP 2009d,
p. 2). The Mount Logan Mine
occurrence grows on lands owned by
both the energy development company
(approximately 90 percent) and BLM (10
percent), and has 533 plants (CNHP
2009a, p. 1).
Two additional Penstemon debilis
occurrences on BLM land are
considered to have ‘‘poor’’ estimated
viability (CNHP 2009e, p. 1; CNHP
2009f, p. 1). The Anvil Points
occurrence had 200 to 300 plants
reported in 1994, but only three plants
could be found in 1998 (CNHP 2009e,
p. 1). The latest survey in 2006 found
no plants at this occurrence (CNHP
2009e, p. 1). It appears that the decline
of this occurrence was a result of natural
processes including competition by
surrounding vegetation (DeYoung
2008a, p. 1). The area including this
habitat also was leased under the BLM
August 2008 lease sale (BLM 2008b, p.
3; Ewing 2008a, p. 7).
The Mount Logan Road occurrence,
discovered in 1996 on a road cut, had
10 plants, of which only 3 were found
in 2005 (CNHP 2009f, p. 1). Because
these two occurrences have so few
individuals, they are considered to have
poor viability by CNHP, and we
consider them not viable into the future.
The Smith Gulch occurrence of
approximately 12 plants was reported in
June 2009 (Graham 2009a, pp. 1–2).
This occurrence has not been rated by
CNHP; however, it is small (12 plants)
and, because of its positioning in a
drainage, has a high potential for being
destroyed by a rain event (Graham
2009a, pp. 1–2).
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TABLE 2. CURRENT AND HISTORICALLY KNOWN Penstemon debilis OCCURRENCES
Occurrence
Viability
# of Plants
ac (ha)
Land Ownership
Mt. Callahan Natural Area
Excellent
2,100-2,240
32 (12.9)
Private
Anvil Points Road
Good
700
5 (2)
BLM
Mount Logan Mine
Good
533(50 on BLM)
2 (0.8)
Private and BLM
Mount Callahan Ridge
Good
650
4 (1.6)
Private
Mount Logan Road
Poor
3
7 (2.8)
BLM
Anvil Points
Poor
0
6 (2.4)
BLM
Smith Gulch
Unrated
12
not reported
BLM
Total
3,998 – 4,138
56 (22.7)
The total estimated number of
Penstemon debilis in the wild is
currently 3,998 to 4,138 individuals.
The occurrences on BLM land represent
about 18 percent of the total plants
counted and estimated. An energy
development company owns land that
contains approximately 82 percent of
the total plants. We have no information
to indicate an overall species trend.
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Summary of Factors Affecting
Penstemon debilis
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Penstemon debilis habitat is
threatened by energy development and
associated impacts. Of the four known
viable occurrences (Mount Callahan
Natural Area, Anvil Points Road, Mount
Logan Mine, Mount Callahan Ridge), all
but the Anvil Points Road occurrence
are on lands wholly or partially owned
by an energy development company. All
four viable occurrences, which exist on
the Roan Plateau, face ongoing or
potential threats, including: oil and gas
development, oil shale extraction and
mine reclamation, and road
maintenance and vehicle access through
occurrences.
The Piceance Basin, including federal
and private lands surrounding the Roan
Plateau, has experienced a boom in
natural gas production in recent years.
The BLM projects that around 3,916
billion cubic feet of natural gas will be
developed over the next 20 years from
the portion of the Roan Plateau that was
addressed in the new RMP amendment
(CNE 2004a, p. 44). Oil and gas
exploration and development continues
to increase each year on and around the
Roan Plateau. In 2003, 566 new wells
were permitted in Garfield County: 796
in 2004; 1,508 in 2005 (Colorado Oil
and Gas Conservation Commission
(COGCC 2006, p. 1); 1,844 in 2006;
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2,550 in 2007 (COGCC 2008, p. 1); and
2,888 in 2008 (COGCC 2009a, p. 1).
Because of a decrease in natural gas
prices, new well permits decreased in
2009 to 743 (Webb 2009, p. 1), as of June
3, 2009 (COGCC 2009a, p. 1). This
number is down from the 1,029 wells
permitted by the same time in 2008, but
is still higher than the 566 wells
permitted in Garfield county in all of
2003 (COGCC 2008, p. 1).
Energy exploration and development
includes construction of new unpaved
roads, well pads, disposal pits,
evaporation ponds, and pipeline
corridors, as well as cross country travel
by employees. Each of these actions has
the potential to cause direct impacts
such as plant removal and trampling,
and indirect impacts to Penstemon
debilis such as dust deposition and loss
of habitat for pollinators. The
ramifications of direct impacts are easily
assessed if witnessed. Plant removal,
contact with herbicide or ice-melting
chemicals, and trampling can cause
death of plants. Because P. debilis was
unknown as a species until 1987, and
most of the occurrences are on private
land or in remote locations on public
land, the impacts may go unnoticed. For
example, impacts to the Mount Logan
Mine occurrence were unknown until
the occurrence was discovered in 2005;
even after discovery, further minerelated impacts occurred because the
remote location of the mine made it
difficult for BLM to manage the
occurrence (CNHP 2009b, p. 1; Ewing
2009a, p. 4).
Indirect effects to Penstemon debilis
from energy exploration are less easily
assessed. Road traffic on unpaved roads
increases dust emissions in previously
stable surfaces (Reynolds et al. 2001, p.
7126). For every vehicle traveling one
mile (1.6 km) of unpaved roadway once
a day, every day for a year,
approximately 2.5 tons of dust are
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deposited along a 1,000-foot (305-m)
corridor centered on the road (Sanders
2008, p. 20). Vascular plants can be
greatly affected within the zone of
maximum dust fall (i.e., the first 1000 ft
(305 m) from the road) (Everett 1980, p.
128). Excessive dust may affect
photosynthesis, affect gas and water
exchange, clog plant pores, and increase
leaf temperature leading to decreased
plant vigor and growth (Ferguson et al.
1999, p. 2; Sharifi et al. 1997, p. 842).
All of the viable occurrences of P.
debilis are within 300 ft (91 m) of roads.
Further energy development would
likely increase road density and traffic
volume.
Other indirect impacts can occur due
to a loss of pollinator habitat.
Penstemon debilis requires an insect
pollinator to reproduce (McMullen
1998, p. iii). McMullen (1998)
concluded that pollinators for P. debilis
were generalists and were not limiting
at that time (prior to the energy boom).
However, Tepedino (2009) described
how the pollination biology of another
Piceance Basin rare plant (Physaria
obcordata) is being impacted by energy
development. He described that any
energy development that reduces the
general level of available floral
vegetation has a detrimental effect on
pollinators’ ability to reproduce,
subsequently resulting in fewer
pollinators and reduced ability of the
dependent plant to reproduce (Tepedino
2009, pp. 16–17).
A large parcel of land including
habitat occupied by the Anvil Points
Road occurrence was offered and sold
for oil and gas leasing under the BLM
August 2008 lease sale (DeYoung 2008b,
p. 1; BLM 2008b, p. 1; Ewing 2008a, p.
7). This lease is currently being
contested in court. Increased energy
exploration in the Anvil Points Road
area may increase maintenance and
vehicle access on the unstable road that
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transects the Penstemon debilis
occurrence and increase the likelihood
of effects to P. debilis due to
construction of additional roads and
other facilities associated with oil and
gas exploration.
Oil shale mining has impacted
Penstemon debilis occurrences. Oil
shale extraction activities occurred on
the Roan Plateau in the early 1980s and
into the 1990s (COBiz 2008, pp. 3–4).
This extraction impacted the Mount
Logan Mine and Anvil Points Road
occurrences. Because P. debilis was not
identified as a species until 1987, we
have no record of the pre-mining
occurrence status. However, we believe
the plants were present at these sites
prior to mining because they are present
now. The plants were likely heavily
impacted by mine operations within
their habitat, and the occurrences have
recovered to a far smaller population
size on a reduced area of habitat (see
Factor E for discussion of inherent risk
of small population size).
Commercial oil shale extraction has
not yet proven to be economically
viable, and current research and
development efforts no longer focus on
surface mining of oil shale rock on the
Roan Cliffs (COBiz 1987, pp. 3–4). The
BLM recently released the RMP
amendments to allow oil shale leasing
in the Piceance Basin (BLM 2007a, p. 1).
The known Penstemon debilis
occurrences are not within the area that
BLM has currently identified as
available for leasing (BLM 2008c, p. 14).
It is unknown when oil shale extraction
will become economically viable.
Despite the recent retreat from surface
mining of oil shale, if commercial oil
shale production does become
economically viable, we expect a
renewed interest in extracting shale
from the cliffs of the Roan Plateau
because of the convenient access to
shale resources on the surface. Recent
and ongoing impacts to the Anvil Points
Road occurrence are occurring due to
research conducted by an oil shale
research and development company and
at the Anvil Points Road and Mount
Logan Mine occurrences due to mine
reclamation and closure efforts
(DeYoung 2009a, pers. comm.; Mayo
2006, pp. 1–4).
The BLM has begun mine reclamation
action under the Comprehensive
Environmental Response,
Compensation, and Liability Act
(CERCLA) (42 U.S.C. 9601 et seq.),
commonly known as Superfund, to
remove health and safety hazards from
Anvil Points Road. Actions will include
closing access to the passages leading
into the mine and removing lead mine
tailings soil on the mine bench
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(Goodenow 2008, pers. comm.). It is
unknown whether the lead in the soil is
a threat to Penstemon debilis. The
CNHP estimates 700 individual plants at
this occurrence (CNHP 2009d, p. 2). To
date, 88 plants are known to have been
directly impacted by Anvil Points Road
mine reclamation actionspermitted by
BLM, occuring in the winter of 20082009 (DeYoung 2009b, pers. comm.). Of
the 88, 21 were transplanted, and 67
were covered by matting intended to
reduce soil disturbance (DeYoung
2009b, pers. comm.; DeYoung 2009c, p.
1). Long-term success of transplants is
unknown, but 2 of the 21 transplants
died as of June 2009 (DeYoung 2009c,
p. 1). Eleven of the 67 plants covered by
matting are dead or unaccounted for
(DeYoung 2009c, p. 1). With restoration
work still underway, it is unclear how
many more plants will be impacted.
The Anvil Points Road occurrence is
impacted by Garfield County road
stabilization work, which is required to
maintain access to a transmitter tower
located within occupied habitat for
Penstemon debilis. In addition, BLM
recently allowed an oil shale research
and development company to conduct
research in the Anvil Points mine, a
project area containing the Anvil Points
Road occurrence (Ewing 2008a, p. 4).
This research consists of taking high
resolution photographs of the geologic
formation visible from the sides of the
mine, and possibly removing core
samples. This research project is
expected to include vehicle trips up the
road every day for 1 month and to
directly impact P. debilis individuals
growing in the road immediately
outside the mine (Ewing 2008a, p. 6).
The roads transecting the occurrence are
on shifting shale talus slopes and are
very conducive to rock and mudslides,
which can destroy P. debilis habitat and
which require the road to be maintained
frequently. Three plants are known to
have been destroyed by the road
maintenance conducted under this
permit (DeYoung 2009a, pers. comm.).
The BLM believes that some additional
plants may have been trampled by
unauthorized access to an area that was
fenced off during the research period;
however, it is unclear how many plants
were disturbed (DeYoung 2008c, pers.
comm.). In addition to the direct
impacts, the road maintenance required
to allow this level of traffic makes
occupied P. debilis habitat more
accessible to the public, which could
result in further trampling by humans
and vehicles (Ewing 2008a, pp. 5–6).
The Mount Logan Mine occurrence of
Penstemon debilis is primarily located
on land owned by a natural gas and oil
shale production corporation, with a
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portion of the occurrence occupying
BLM land. This occurrence is perched
on a steep, unstable slope above a road
that is currently used for access to an
ongoing reclamation project at an old oil
shale mine site. Several plants on this
steep road bank were dangling by their
roots in 2005 due to road maintenance
(Mayo 2006, pp. 1–4). The road was
widened, and these plants were gone by
2006 (Mayo 2006, p. 1). Mine
reclamation actions destroyed a portion
of this occurrence by burying it in
topsoil (Ewing 2009a, p. 4). This site
also contains noxious weeds associated
with the disturbance; it is unknown
whether the weeds will pose a threat to
P. debilis (Ewing 2009a, p. 4). The BLM
portion of this occurrence was included
in an oil and gas lease parcel nominated
for sale; however, BLM deferred the sale
of the lease parcel until their RMP
revision is complete, and until we make
a decision concerning the status of the
species (CNE 2005, p. 1; Lincoln 2009,
pers. comm.). The energy company that
owns the land containing most of the
Mount Logan Mine occurrence has been
actively developing their holdings in
this area. Further development of the
lands immediately surrounding this
occurrence would likely result in
impacts due to road construction and
maintenance on the unstable shifting
shale talus.
The Mount Logan Road occurrence,
located on a road cut near the Logan
Mine occurrence, had 10 plants in 1996,
of which only 3 plants were found in
2005 (CNHP 2009f, p. 1). This
occurrence has no barriers to shield the
plants from road impacts, such as
removal by maintenance machinery,
accidental trampling, and spraying of
ice melting or herbicide chemicals; the
road also generates heavy dust (CNHP
2009f, pp. 1–3; DeYoung 2009d, pp. 1–
3; Ewing 2009a, p. 2). As a result of
these threats, we consider this
occurrence to be nonviable.
The Mount Callahan Natural Area and
Mount Callahan Ridge occurrences,
which include approximately 82
percent of total known Penstemon
debilis plants, occur on land owned by
an energy development company. These
occurrences are behind locked gates,
making them inaccessible to the public
and the Service. The landowner intends
to develop up to three natural gas well
drilling pads within a 680-ac (275-ha)
area that includes both Mount Callahan
occurrences (Webb 2008, p. 1).
Construction has begun on one pad,
located 360 ft (110 m) from the nearest
known P. debilis individual and 105 ft
(32 m) uphill from its habitat (Ewing
2008a, p. 2). These pads will likely
indirectly impact P. debilis through dust
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generation, loss of pollinator habitat,
and inadvertent trampling by employees
and contractors. Monitoring of the
occurrence, in connection to the energy
development, has resulted in trampling
of individual plants by people collecting
the data (Ewing 2009a, p. 1).
The Smith Gulch occurrence of
approximately 12 plants was discovered
on BLM lands below Mount Callahan
during surveys for a proposed oil and
gas development project in June 2009
(Graham 2009b, p. 1). Two well pads,
and corresponding roads and pipelines,
are proposed for this area (Graham
2009b, p. 1).
The BLM develops a Reasonably
Foreseeable Development scenario
(RFD) to project the level of oil and gas
activity that can be expected to occur.
The RFD is intended as a technical and
scientific approximation of anticipated
levels of oil and gas development during
the planning timeframe (BLM 2006, p.
4–2). It is not intended to define specific
numbers and locations of wells and
pads. An RFD for oil and gas is a longterm projection of oil and gas
exploration, development, production,
and reclamation activity within the
lands and minerals managed by the
BLM Field Office (BLM 2005b, p. 2).
The RFD is a technical report typically
referenced in the NEPA document for
the RMP (BLM 2005b, p. 2).
The RFD for the Glenwood Springs
BLM Field Office, Roan Plateau
Planning Area, which contains the
Anvil Points Road and Anvil Points
Penstemon debilis occurrences, used 20
years as the foreseeable development
timeframe. Based on the RFD, the Roan
Environmental Impact Statement (EIS)
Proposed Plan projected approximately
669 pads, 3,691 wells, 2,791 ac (1,129
ha) of long-term disturbance, and 1,624
ac (657 ha) of short-term disturbance in
the Roan Planning Area (BLM 2006, p.
4–11). The other occurrences located on
BLM land (Mount Logan Mine and
Mount Logan Road) are within the BLM
Grand Junction Field Office, which is
currently in the process of developing a
new RFD. The current RFD was
developed in 1987, and forecasted 50
wells a year for a 20–year timeframe
(Anderson 2008, p. 1). No RFD
projection is available for the lands
containing the Mount Callahan Natural
Area, Mount Callahan Ridge, and
private portion of the Mount Logan
Mine occurrences, because they are on
private lands with privately owned
minerals.
Penstemon debilis is not protected by
Federal regulation for about 82 percent
of the total known and estimated plants
because they are on private land. The
remaining 18 percent of plants are on
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BLM lands. The BLM controls access to
the Anvil Points Mine (containing the
Anvil Points Road occurrence) with a
gate. This gate is often left open,
allowing public access to the plant
occurrence Access to the other BLM
occurrence (the Mount Logan Road
occurrence) is controlled by a guard
station. Approximately 300 trucks,
associated with energy development,
drive by this occurrence every day after
checking with the guard (Mayo 2005, p.
1).
In summary, three of the four viable
occurrences (Mount Callahan Natural
Area, Mount Logan Mine, and Mount
Callahan Ridge) are on lands owned
wholly or partially by an energy
development company. Some
individuals of the fourth occurrence
(Anvil Points Road), on BLM land, are
subject to transplantation or destruction
as a result of an ongoing mine
restoration project and road
maintenance. Over the past 6 years, oil
and gas exploration and production has
increased substantially in the area
containing the habitat for Penstemon
debilis making it likely that the species
will become endangered in the
foreseeable future. The pace of new
development slowed in 2009; however,
it is still far above pre-2004 levels. P.
debilis grows on steep shifting slopes,
and roads through P. debilis habitat are
unstable and require frequent
maintenance, which often destroys
plants. Plants seem to be able to
recolonize their habitat after
disturbance; however, recolonization is
slow, and would not be able to keep
pace with rapid development. For these
reasons we consider destruction and
modification of the species’ habitat for
natural gas production, oil shale mining,
mine reclamation, road maintenance,
and associated impacts resulting from
increased vehicle access to the
occurrences, a moderate but immediate
threat to P. debilis.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Overutilization for commercial,
recreational, scientific, or educational
purposes is not known to be a threat to
Penstemon debilis. Therefore, this factor
is not addressed in this proposal.
C. Disease or Predation
Seed predation of Penstemon debilis
by small mammals has shown to be very
low (McMullen 1998, pp. 39–40).
Grazing, predation, and disease are not
known to be a threat to P. debilis.
Therefore, this factor is not addressed in
this proposal.
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D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
Approximately 82 percent of
Penstemon debilis occupied habitat
occurs on private lands. We are not
aware of any city or county ordinances
or zoning that provide for protection or
conservation of P. debilis or its habitat.
State Laws and Regulations
No State laws or regulations protect
rare plant species in Colorado on private
land or otherwise. The Mount Callahan
Natural Area and Mount Callahan Ridge
occurrences, including approximately
82 percent of total known Penstemon
debilis plants, occur on land owned by
an energy development company. With
the cooperation of the landowner, the
CNAP, a State agency, has designated
the area of Mount Callahan (referred to
throughout the document as the Mount
Callahan Natural Area occurrence) and
Mount Callahan Ridge occurrences as
Natural Areas (Kurzel 2008, pers.
comm.; CNAP 1987, pp. 1–7;, CNAP
2008a, pp. 1–7;, Webb 2008, p. 1)
Through these designations, the
landowner has agreed to develop the
natural gas pads in a way that should
minimize impacts to the P. debilis
occurrences (Ewing 2008a, pp. 1–2). The
agreements include conservation
measures such as stormwater
management and a noxious weeds
management plan in order to minimize
development impacts to the species
(CNAP 2008b, pp. 1–4; CNAP 2008c, pp.
1–4). The CNAP has been very
successful in garnering landowner
participation in conservation of rare
species in Colorado. However, natural
area agreements are voluntary and can
be terminated at any time by either
party with a 90-day written notice. For
this reason, and because no legally
binding conservation easements or
candidate conservation agreements
protect any of the occurrences on
private land, we have concluded that
the Natural Area designation alone does
not constitute an adequate regulatory
mechanism to conserve P. debilis. We
consider inadequate State laws and
regulations a significant and immediate
threat to this species, because the laws
do not ameliorate the threats to the
species.
Federal Laws and Regulations
The Federal Land Policy and
Management Act (FLPMA) (43 U.S.C.
1701 et seq.) directs BLM, as part of the
land use planning process, to ‘‘give
priority to the designation and
protection of areas of critical
environmental concern’’ (Sec. 202(c)(3)).
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The FLPMA defines areas of critical
environmental concern (ACECs) as
‘‘areas within public lands where special
management attention is required ... to
protect and prevent irreparable damage
to important historic, cultural, or scenic
values, fish and wildlife resources or
other natural systems or processes, or to
protect life and safety from natural
hazards’’ (Sec. 103 (a)). Designation as
an ACEC recognizes an area as
possessing relevant and important
values that would be at risk without
special management attention (BLM
2006, pp. 3–110). The ACEC designation
carries no protective stipulations in and
of itself (BLM 2006, pp. 2–65).
Following an evaluation of the
relevance and importance of the values
found in potential ACECs, a
determination is made as to whether
special management is required to
protect those values and, if so, to specify
what management prescriptions would
provide that special management (BLM
2006, pp. 3–111). The Records of
Decision (RODs) for the Roan Plateau
RMP Amendment were signed June 8,
2007, and March 12, 2008. The March
12, 2008, ROD establishes the Anvil
Points ACEC, an area designated for
management of sensitive resources
including Penstemon debilis (BLM
2008a, ROD p. 4). The ROD lists as an
objective for the Anvil Points ACEC to
‘‘protect occupied habitat and the
immediately adjacent ecosystem
processes that support candidate
plants.’’ This ROD also authorizes oil
and gas development in the ACECs,
making the portions of these areas that
are not currently leased, available for
lease (BLM 2008a, ROD p. 2). Anvil
Points ACEC covers most of the
formerly occupied occurrence area at
Anvil Points, and the entire Anvil
Points Road occurrence.
In order to protect Penstemon debilis
in the ACEC, a No Surface Occupancy
(NSO) and No Ground Disturbance
(NGD) stipulation was established for
both Anvil Points P. debilis occurrences
(BLM 2007b, ROD p. 26). The term NGD
applies to all activities except oil and
gas leasing and permitting, while the
term NSO applies only to oil and gas
leasing and permitting (BLM 2008a,
ROD p. 6). The NSO designation
prohibits long-term use or occupancy of
the land surface for fluid mineral
exploration or development to protect
identified resource values (BLM 2006,
pp. 2–3). This designation means that an
area is protected from permanent
structures or long-term grounddisturbing activities (i.e., lasting longer
than 2 years) (BLM 2006, pp. 2–3). For
example, an NSO designation would
preclude construction of a well pad
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(because it would last longer than 2
years) but not a typical pipeline
(because it would be revegetated within
2 years) (BLM 2006, pp. 2–3). Also, an
NSO does not preclude the extraction of
underlying fluid minerals if they can be
accessed from outside the area by
directional drilling (BLM 2006, pp. 2–3).
Directional drilling may not disturb the
overlying surface, including Penstemon
debilis habitat. Except for specified
situations, individual NSOs may
include exceptions so that BLM may
allow a ground-disturbing activity if it
meets specific, stated criteria (BLM
2006, pp. 2–3). For example, the NSO
designation for these occurrences allows
for the BLM to grant exceptions for longterm ground disturbing activities if
consultation with the Service indicates
that proposed activity would not impair
maintenance or recovery of the species
(BLM 2007a, pp. F6-F7).
The protections provided by the NSO/
NGD provision of the ACEC designation
should be adequate to provide for
maintenance of the Anvil Points Road
occurrence. When applied, the NSO/
NGD would require BLM to consult
with the Service and ensure that
proposed activity would not impair
maintenance or recovery of the species
prior to authorizing an exception to the
NSO/NGD (BLM 2007a, pp. F6-F7).
However, despite NSO/NGD provisions,
projects have proceeded without
consultation that resulted in destruction
of Penstemon debilis individuals, and
other projects with likely impacts to P.
debilis are being considered by BLM
without consultation. This ability to
proceed without consultation indicates
that the NSO/NGD provisions are
inadequate to protect P. debilis and its
habitat. Recent examples demonstrating
the inadequacy of the NSO/NGD
provisions follow. (1) The BLM
approved work under the CERCLA to
remove health and safety hazards from
the Anvil Points Road occurrence. This
project resulted in direct impacts to at
least 90 Penstemon debilis individuals
(DeYoung 2009c, p. 1). We believe many
of these impacts could have been
avoided or minimized through the
consultation process. (2) BLM is
considering granting permission for
continued maintenance of the Garfield
County transmitter tower access road
(DeYoung 2009b pers. comm.).
Maintaining the existing road rather
than relocating it increases the
likelihood of destroying P. debilis plants
and prevents the recolonization of
plants in the current road bed. (3) BLM
has authorized oil shale research
projects in the past at the Anvil Points
mine (Ewing 2008a, p.4), which lead to
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the destruction of P. debilis plants (BLM
2007a, p. F6-F7; DeYoung 2009a, pers.
comm.). (4) The land containing the
Anvil Points Road occurrence was
leased for oil and gas development
under the BLM August lease sale
(DeYoung 2008b, p. 1; BLM 2008b, p. 1;
Ewing 2008a, p. 7). Increased energy
exploration in the Anvil Points Road
area may increase maintenance and
vehicle access and consequently
increase the likelihood of other adverse
affects. Continued adverse impacts to
the Anvil Points Road occurrence,
beyond those currently occurring during
the mine reclamation effort, could result
in reduced viability and possible
extirpation of the Anvil Points Road
occurrence.
In summary, we found that existing
regulatory mechanisms are inadequate
to protect Penstemon debilis. No State
or local laws or regulations protect
Penstemon debilis. P. debilis is afforded
some protection on Federal lands as a
candidate species; however, the
protection has been inadequate, and
would be reduced if we find that P.
debilis does not meet the definition of
an endangered or threatened species. P.
debilis has no regulatory protection for
approximately 82 percent of the total
estimated plants because they are on
private land. The private land owner
has pledged to protect these plants from
direct impacts, but the agreement is not
legally binding. Because of this lack of
regulation, we consider inadequate
regulatory mechanisms to be a
significant and immediate threat to this
species.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
The Anvil Points occurrence, which
formerly included several hundred
plants on BLM land, has been reduced
to zero plants since 1994 for unknown
reasons (CNHP 2009e, p. 1). It appears
that the decline of this occurrence was
a result of natural processes including
competition by surrounding native
vegetation, which includes
Chrysothamnus viscidiflorus (yellow
rabbitbrush) (DeYoung 2008a, p. 1;
CNHP 2009e, p. 2). New Penstemon
debilis plants grown off site from seeds
were introduced but declined over
several years (CNHP 2009e, p. 2).
Monitoring failed to show a cause for
the disappearance of P. debilis
(DeYoung 2008a, p. 1).
Penstemon debilis population sizes
are small, and the smaller the
population, the more likely extinction is
in any given period of time (Shaffer
1987, p. 70). All occurrences of P.
debilis grow on a 17-mi (27-km) stretch
of the rim of the Roan Plateau in
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Garfield County, Colorado (Ewing
2008a, p. 7). The two largest
occurrences are within 2 mi (3 km) of
each other (Ewing 2008a, p. 7). A
species with such a small range could
be particularly susceptible to extirpation
from a stochastic event such as an
earthquake, rockslide, or severe hail
storm (McMullen 1998, p. 3). This
increased susceptibility is due to the
likelihood that, although stochastic
events are often localized in severity,
such a localized event would likely
impact all occurrences of the species,
rather than just a small portion of the
occurrences, as may be expected for a
species with a larger range. For
example, the newly discovered Smith
Gulch occurrence is small (12 plants),
and because of its positioning in a
drainage, has a high potential for being
destroyed by a rain event (DeYoung
2009e, p. 1).
In addition, the fragmentation of P.
debilis habitat by human-related
activities threatens to reduce the species
to mosaics of small populations
occurring in isolated habitat remnants.
Occurrences with small population size
(fewer than 50 individuals) are more
likely to suffer genetic problems such as
genetic drift and inbreeding depression
due to losses of individuals in such
events (McMullen 1998, p. 3; Ellstrand
& Elam 1993, p. 226). Conversely, if the
current population structure is similar
to the historical range, it is possible that
P. debilis has adapted to be less
vulnerable to inbreeding depression
(Ellstrand & Elam 1993, p. 225).
Climate change could potentially
impact Penstemon debilis. According to
the Intergovernmental Panel on Climate
Change (IPCC), ‘‘Warming of the climate
system in recent decades is
unequivocal, as is now evident from
observations of increases in global
average air and ocean temperatures,
widespread melting of snow and ice,
and rising global sea level’’ (Bates et al.
2008, p. 15). Average Northern
Hemisphere temperatures during the
second half of the 20th century were
very likely higher than during any other
50–year period in the last 500 years and
likely the highest in at least the past
1,300 years (IPCC 2007, p. 30). It is very
likely that over the past 50 years, cold
days, cold nights, and frosts have
become less frequent over most land
areas, and hot days and hot nights have
become more frequent. It is likely that
heat waves have become more frequent
over most land areas, and the frequency
of heavy precipitation events has
increased over most areas (IPCC 2007, p.
30). As described above, climate
modeling is not currently to the level
that we can predict the amount of
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temperature and precipitation change
within P. debilis’s limited range.
Therefore, we generally address what
could happen under the current climate
predictions. However, we need further
refinement of the current predictions to
draw more reliable conclusions
concerning the effects of climate change
on the species.
It is unknown how Penstemon debilis
responds to drought; however, in
general, plant numbers decrease during
drought years, but recover in subsequent
seasons that are less dry. Drought years
could result in a loss of plants. Changes
in the global climate system during the
21st century are likely to be larger than
those observed during the 20th century.
For the next 2 decades, a warming of
about 32.4 °F (0.2 °C) per decade is
projected (IPCC 2007, p. 45). Afterward,
temperature projections increasingly
depend on specific emission scenarios.
Various emissions scenarios suggest that
by the end of the 21st century, average
global temperatures are expected to
increase 33 to 39 °F (0.6 to 4.0 °C) with
the greatest warming expected over
land. Localized projections suggest the
Southwest may experience the greatest
temperature increase of any area in the
lower 48 States. It is likely that hot
extremes, heat waves, and heavy
precipitation will increase in frequency
(IPCC 2007, p. 30). There also is high
confidence that many semi-arid areas
like the western United States will
suffer a decrease in water resources due
to climate change. A 10- to 30-percent
decrease in precipitation in mid-latitude
western North America is projected by
the year 2050 based on an ensemble of
12 climate models (Milly et al. 2005, p.
1). When plant populations are
impacted by additional threats during
drought years, they may require several
years to recover. Climate change may
exacerbate the frequency and intensity
of droughts. Under drought conditions,
plants generally are less vigorous and
less successful in reproduction. With
small populations and their inherent
genetic risk, lowered reproduction
could result in reduced population
viability.
Recent analyses of long-term data sets
show accelerating rates of climate
change over the past 2 or 3 decades,
indicating that the extension of species’
geographic range boundaries towards
the poles or to higher elevations by
progressive establishment of new local
populations will become increasingly
apparent in the relatively short term
(Hughes 2000, p. 60). The limited
geographic range of the oil shale
substrate that makes up the entire
Penstemon debilis habitat could limit
the ability of the species to adapt to
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35733
changes in climatic conditions by
progressive establishment of new
populations.
Incidental disturbance by humans,
and stochastic events, such as drought,
landslides, or encroaching vegetation
can impact Penstemon debilis. However
the species likely evolved under these
factors and we do not consider them
significant immediate threats. Climate
change could exacerbate these factors,
causing them to pose a threat to P.
debilis; however the current data are not
reliable enough at the local level for us
to draw conclusions regarding the
imminence of climate change threats to
P. debilis.
Background—Phacelia submutica
Previous Federal Actions
We included Phacelia submutica as a
category 1 candidate species in the 1980
Review of Plant Taxa for Listing as
Endangered or Threatened Species (45
FR 82480, December 15, 1980). In that
notice, category 1 candidates were
defined as species for which the Service
had ‘‘sufficient information on hand to
support the biological appropriateness
of their being listed as Endangered or
Threatened species.’’ We changed the
candidate status of P. submutica to
category 2 on November 28, 1983 (45 FR
82480). On February 21, 1990, we again
identified P. submutica as a category 1
candidate species (55 FR 6184). In the
February 28, 1996, Federal Register (61
FR 7596) all category 1 candidate
species became candidates under the
current definition. We assigned P.
submutica an LPN of 11. In the 2005
CNOR (70 FR 24870, May 11, 2005) we
raised the LPN to 8, to reflect the
increasing level of threats, which are
imminent and of moderate magnitude.
On May 11, 2004, we received a
petition from the CBD to list, as
endangered, 225 species we previously
had identified as candidates for listing,
including Phacelia submutica (CBD
2004, p. 146). Under requirements in
section 4(b)(3)(B) of the Act, the CNOR
and the Notice of Findings on
Resubmitted Petitions published by the
Service on May 11, 2005 (70 FR 24870),
included a finding that the immediate
issuance of a proposed listing rule and
the timely promulgation of a final rule
for each of these petitioned species,
including P. submutica, was warranted
but precluded by higher priority listing
actions, and that expeditious progress
was being made to add qualified species
to the Lists.
On April 28, 2005, the CNE, the
Colorado Native Plant Society, and
botanist Steve O’Kane, Jr., Ph.D.,
submitted a petition to the Service to
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list Phacelia submutica as endangered
or threatened within its known
historical range, and to designate critical
habitat concurrent with the listing (CNE
et al. 2005, p. 1). We considered the
information in the petition when we
prepared the 2006 CNOR (71 FR 53756,
September 12, 2006). Section 4(b)(3)(C)
of the Act requires that when we make
a warranted-but-precluded finding on a
petition, we are to treat such a petition
as one that is resubmitted on the date of
such a finding. We identified P.
submutica as a species for which we
made a continued warranted-butprecluded finding on a resubmitted
petition in the Federal Register on
December 6, 2007 (72 FR 69034), and
December 10, 2008 (73 FR 75176). We
retained an LPN of 8 for the species. In
the 2008 notice, we announced that we
have not updated our assessment for
this species, as we were developing this
proposed listing rule (73 FR 75227).
In each assessment since its
recognition as a candidate species under
the current definition in 1996, we
determined that publication of a
proposed rule to list the species was
precluded by our work on higher
priority listing actions. In 2008, we
received funding to initiate the proposal
to list Phacelia submutica.
Species Information
Phacelia submutica is a rare annual
plant endemic to clay soils derived from
the Atwell Gulch and Shire members of
the Wasatch Formation in Mesa and
Garfield Counties, Colorado. The 25
known occurrences of the plant occupy
a total of 104 ac (42 ha) (CNHP 2009g,
records a-hh; CNHP 2010, records ii-jj;
WestWater Engineering 2004, pp. 2;
Ewing 2008b, map). Fifteen of the
occurrences occupy patches of 1 ac (0.4
ha) or less. All occurrences consist of
small patches of plants on uniquely
suitable soil separated by larger areas of
similar soils that are not occupied by P.
submutica. The estimated total number
of plants differs from 84 to 42,926 per
year, depending on growing conditions.
The species depends on its seed bank to
survive for one or many years, again
depending on growing conditions.
Phacelia submutica was first
described by Howell based on
specimens collected from the town of
DeBeque, Mesa County, Colorado, in
1911 and 1912 (Howell 1944, pp. 370–
371Halse (1981, pp. 121, 129, 130)
reduced it to varietal status as P.
scopulina var. submutica. This has been
challenged as incorrect by O’Kane
(1987, p. 2), who claimed Halse used
inadequate collection materials, and
that P. submutica is geographically
isolated from P. scopulina (O’Kane
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1987, p. 2; 1988, p. 462). Phacelia
submutica is recognized at the species
rank by current floristic treatments in
Weber and Wittmann (1992, p. 98; 2001,
p. 203) and by the Director of the Biota
of North America Program (Kartesz
2008, pers. comm.). While the Integrated
Taxonomic Information System (2001)
database cites John Kartesz as the expert
source for this species, it is not updated
with his currently accepted name for the
species: Phacelia submutica (Kartesz
2008, pers. comm.). Phacelia is included
in the Hydrophyllaceae (waterleaf
family). Recent molecular data suggest
that this family should be combined in
an expanded Boraginaceae (borage
family). There are conflicting views on
the configuration of this larger
Boraginaceae and the lead author of the
family treatment for the upcoming Flora
of North America has chosen to retain
the Hydrophyllaceae. Therefore, we will
retain Phacelia in the Hydrophyllaceae
family for this proposal.
Phacelia submutica is a low-growing,
herbaceous, spring annual plant with a
tap root. The stems are typically 0.8 to
3 in. (2 to 8 cm) long, often branched at
the base and mostly laying flat on the
ground as a low rosette (Howell 1944,
pp. 371–372). Stems are often deep red
and more or less hairy with straight
andstiff hairs. Leaves are similarly
hairy, reddish at maturity, 0.2 to 0.6 in.
(5 to 15 mm) long, egg-shaped or almost
rectangular with rounded corners, with
bases abruptly tapering to a wedgeshaped point. Leaf margins are smooth
or toothed. The yellowish flowers are
arranged on somewhat congested
racemes; the stamens are shorter than
the corolla throat and the fruits are not
attenuate at the apex (Howell 1944, pp.
371–372).Unlike many Phacelia species,
the stamens do not protrude beyond the
petals. The style is 0.04 to 0.06 in. (1 to
1.5 mm) long and nearly hairless. The
bracts around the seed capsules are 0.2
to 0.4 in. (6 to 10 mm) long. The
elongated egg-shaped seeds are 0.6 to
0.8 in. (1.5 to 2 mm) long with 6 to 12
crosswise corrugations, and are blackish
brown and somewhat iridescent (Howell
1944, p. 370; Halse 1981, p. 130; O’Kane
1987, p. 3).
Phacelia submutica seeds usually
germinate in early April; the plants may
flower between late April and late June.
Fruit set is from mid-May through late
June. Individuals finish their life cycle
by late June to early July, after which
time they dry up and disintegrate or
blow away, leaving no indication that
the plants were present (Burt and
Spackman 1995, p. 23). The species
grows in a habitat with wide
temperature fluctuations, long drought
periods, and erosive saline soils. Upon
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drying,cracks form in the soils. Seeds
plant themselves by falling into the
cracks that close when wetted, thus
covering the seeds (O’Kane 1988, p. 20).
Plant sites differ in numbers of
flowering plants each year, but there are
no observations of site expansion. Seeds
do not appear to disperse to adjacent
soils. The ideal conditions required for
seeds of this species to germinate are
unknown.
It is likely that the number of
seedlings depends not on total
precipitation but on the temperature
after the first major storm event of the
season (Levine et al. 2008, p. 795).
Phacelia submutica seeds can remain
dormant for 5 years (and probably
longer) until the combination and
timing of temperature and precipitation
are optimal (CNHP 2009g, records a–
hh). Rare annuals that flower every year
are subject to extinction under
fluctuating conditions, because they
exhaust their seed reserves (Meyer et al.
2006, p. 901). Rare ephemeral annuals,
such as P. submutica, that save their
seed bank for the best growing
conditions are more resilient to
fluctuating conditions. P. submutica
numbers at Horsethief Mountain
fluctuated from 1,700 plants in 1986, to
50 in 1992, up to 1,070 in 2003, and
down to only a few from 2006 to 2008
(CNHP 2009g, records q–t). The
fluctuation in numbers indicates that
many seeds remain dormant in the seed
bank during years when few plants can
be found.
Phacelia submutica is restricted to
exposures of chocolate to purplish
brown and dark charcoal gray clay soils
derived from the Atwell Gulch and
Shire members of the Wasatch
Formation (Donnell 1969, pp. M13–
M14; O’Kane 1987, p. 10). These
expansive clay soils are found on
moderately steep slopes, benches, and
ridge tops adjacent to valley floors of the
southern Piceance Basin in Mesa and
Garfield Counties, Colorado. On these
slopes and soils, P. submutica usually
grows only on one unique small spot of
ground that shows a slightly different
texture and color than the similar
surrounding soils (Burt and Spackman
1995, p. 15). We do not have a precise
description of the soil features required
to support this species, but it is clear
that the identified habitat that appears
to be suitable will never be fully
occupied by the plants. The currently
known occupied habitat where the
plants grow covers about 104 ac (42 ha)
(CNHP 2009g, records a–hh; CNHP
2010, records ii–jj; Ewing 2008b, map;
see Table 3 below). About 538 ac (216
ha) of suitable habitat have been
mapped (CNHP 2009g, records a–hh;
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CNHP 2010, records ii–jj). A general
range, encompassing outlying
occurrences of P. submutica, includes
about 86,000 ac (34,800 ha) (WestWater
Engineering 2004, pp. 2, 11; Western
Ecological Resource 2008, pp. 54–65,
100; CNHP 2009g, records a–hh; CNHP
2010, records ii–jj; Ewing 2008b, map).
The growing town of DeBeque and
about 10 mi (16.4 km) of interstate
highway 70 and the Colorado River
bisect the species’ range.
Each occurrence of the species
includes one or more sites that often
cover only a few square meters (O’Kane
1987, p. 16). Twenty-five occurrences of
Phacelia submutica, including 37 sites,
are documented (CNHP 2009g, records
a–hh; WestWater Engineering 2007, p.
26;, CNHP 2010, records ii–jj). Two of
the occurrences were newly recorded in
2009 (CNHP 2010, records ii–jj). All
occurrences are separated from one
another by at least 0.6 mi (1 km) of
unsuitable habitat or 1.2 mi (2 km) of
suitable habitat (CNHP 2007, p, 1). Six
of the 25 occurrences are considered
historical records, and three additional
occurrences have historical sites
included with occupied habitat data.
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Historical occurrences or sites have
either not been revisited for at least 20
years, or they were revisited but no
plants were found within the last 20
years. Historical records are included in
the following table of occurrences and
subsequent analyses of status. The
highest total number of P. submutica
plants that have ever been counted at
the 25 occurrences is 42,926 (see Table
3 below). The lowest total count was 84
plants (CNHP 2009g, records a–hh;
WestWater Engineering 2007, pp. 17, 26;
CNHP 2010, records ii, jj).
Phacelia submutica is classified by
the CNHP as a G2 and S2 species, which
means it is imperiled across its entire
range and within the State of Colorado
(CNHP 2007, p. 1). CNHP ranks the
quality of each occurrence on a scale of
A to E, with A meaning abundant and
viable, and E meaning extant, but no
ranking information is available. There
is also an H rank for historical records.
Ranks are based on the viability and
number of plants, the amount of
anthropogenic (human) disturbance,
and the amount of weed cover and
intact habitat (CNHP 2007, p. 1). No P.
submutica occurrences are ranked A by
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35735
CNHP. Eleven percent are ranked B, 33
percent have a C rank, 19 percent have
a D rank, and 1 percent has an E rank.
The H rank is assigned to 38 percent of
the records (see Table 3 below; CNHP
2009g, records a–hh; CNHP 2010,
records ii–jj).
No occurrences of Phacelia submutica
have been found beyond the described
habitat and range, including the two
new occurrences recorded in 2009
(CNHP 2010, records ii, jj). Surveys for
P. submutica have been conducted
outward from DeBeque as far as the
exposed soil members extend within the
geologic formation (Burt and Spackman
1995, p. 14). CNHP botanists also
conducted surveys for the species as
part of the Garfield County Survey of
Critical Biological Resources without
finding P. submutica in known
locations or in any new areas (Lyon et
al. 2001, pp. 7, 11). CNHP identified
potential habitat beyond the known
range of the species using modeling
techniques (Decker et al. 2005, pp. 9, 13,
18). This new potential habitat has not
yet been verified in the field because P.
submutica plants have not been present
to confirm that it is occupied habitat.
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15:05 Jun 22, 2010
C—Ashmead Draw
f-h
d-e
B—Pyramid Rock
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q-t
u-v
w
F—Dry Fork
G—Mount Low
H—Horsethief Mountain
I—Sulphur Gulch 1*
J—DeBeque West*
x
m-n
E—Coon hollow 1
Fmt 4702
z
L—Coon Hollow 2*
Sfmt 4702
bb
N—DeBeque South
E:\FR\FM\23JNP1.SGM
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ee
ff
gg
hh
ii
jj
none
37
P—Horsethief Creek
Q—Jerry Gulch
R—Sulphur Gulch 3
S—DeBeque East
T—Roan Creek
U—Mount Logan
V—Housetop Mtn., Atwell
Gulch +
W—Plateau Creek State
Wildlife Area +
X—Little Anderson Gulch
TOTALS
+ indicates 2009 data (CNHP 2010, records ii-jj)
cc
O—Moffat Gulch
aa
M—Sulphur Gulch 2*
y
K—Baugh Reservoir*
i-l
D—Logan Wash*
c
A—Pyramid Ridge
Occurrence
none
B
B
C
C
D
D
C
D
D
D
H
H
H
C
H,H
B,C,C,C
H,C
C,E
C,H,D,H
H,H,H
D,C
C
B,H
Site Ranks
84
0
1
0
0
0
0
0
0
0
0
0
0
0
0
0
0
4
0
34
10
0
0
31
4
Low Counts
104
1
1
28
1
1
1
1
1
1
1
1
1
1
1
1
2
13
1
3
4
5
2
20
12
ac
* indicates historical records
42, 926
370
1,700
1,000
30
195
20
25
250
10
20
17
10
150
1,000
500
50
7,500
10,000
400
10,092
5,817
215
2,055
1,500
High Counts
Occupied
42
0.4
0.4
11.3
0.4
0.4
0.4
0.4
0.4
0.4
0.4
0.4
0.4
0.4
0.4
0.4
0.8
5
0.4
1.2
1.6
2
0.8
8
4.8
ha
538
1
2.5
28
2
6
24
8
3
2
2
4
2
2
6
8
4
67
16
19
63
46
14
160
48
ac
Suitable
216
0.4
1
11.3
0.8
2.4
9.7
3
1.2
0.8
0.8
1.6
0.8
0.8
2.4
3
1.6
27
6.5
7.6
25
18.6
5.6
64.7
19.4
ha
State
BLM USFS
BLM
BLM
BLM
BLM
BLM
BLM
BLM
BLM
BLM
BLM
BLM
BLM USFS
BLM
BLM
BLM
BLM
BLM
BLM
BLM
PVT
PVT
PVT
PVT
PVT
PVT
PVT
PVT
Land Ownership
TABLE 3. OCCUPIED AND SUITABLE HABITAT FOR Phacelia submutica (CNHP 2009G, RECORDS A–HH, OBSERVATION DATES 1982 TO 2008; WESTWATER
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Summary of Factors Affecting Phacelia
submutica
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A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Phacelia submutica is threatened with
destruction and modification of its seed
bank and habitat due to ground
disturbance from natural gas
exploration, production and pipelines,
other energy development, expansion of
roads and utilities, the Westwide Energy
Corridor, increased access to the habitat
by off-road vehicles (ORVs), soil
compaction by cattle, and proposed
water reservoir projects. All known
occurrences are in the midst of the third
largest natural gas producing area in
Colorado (Colorado Oil and Gas
Conservation Commission (COGCC
2008, p. 1)).
About 78 percent of the occupied
habitat for the species and 67 percent of
the entire range of Phacelia submutica
are on BLM lands currently leased for
oil and gas drilling (Ewing 2009, map).
An additional 8 ac (3 ha) of occupied P.
submutica habitat within about 65 ac
(26 ha) of suitable habitat may be
opened to natural gas development by
BLM pending development of a new
Resource Management Plan for the
Grand Junction Field Office (Ewing
2008a, pers. comm.; BLM 2005b, p. 5).
About 3 percent of occupied habitat is
on private land owned by energy
companies (Burt and Spackman 1995, p.
25; CNHP 2009g, records f–g). Although
the sale of oil and gas leases by BLM
does not directly impact rare plant
habitat, it indicates the intention to
continue and increase the level of
development in an area that covers a
large portion of the range of P.
submutica. Likewise, COGCC issues
permits to drill that indicate imminent
development at specific sites on private
and Federal lands (COGCC 2009b, pp.
1–3). Ten new drilling permits have
been issued, and 178 natural gas wells
exist within the 86,000-ac (34,800-ha)
range of P. submutica; 60 of the gas
wells are located within the same 640ac (259-ha) section as 18 occurrences of
occupied P. submutica habitat (Ewing
2009, map).
The ongoing threats to habitat
associated with oil and gas development
include well pad and road construction;
installation of pipelines; and
construction of associated buildings,
holding tanks, and other facilities. All of
these actions would destroy the seed
bank of Phacelia submutica where they
occur on occupied habitat for the
species, and modify suitable habitat so
that the plants cannot grow there,
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making it likely that the species is in
danger of extinction.
The Energy Policy Act of 2005 (42
U.S.C. 15801 et seq.)) directed the
Secretaries of Agriculture, Commerce,
Defense, Energy, and Interior to
designate energy transport corridors for
oil, gas, and hydrogen pipelines and
electricity transmission and distribution
facilities on Federal lands. A portion of
the designated Westwide Energy
Corridor crosses 16,326 ac (6,621 ha) of
BLM land within the range of Phacelia
submutica. Nine of the species’ 25
occurrences are located within this
energy corridor, including 8 ac (3.2 ha),
or about 8 percent, of occupied habitat
and 290 ac (117 ha), or 54 percent, of
suitable habitat (Westwide 2009, map;
Ewing 2009, map). Pipeline and
transmission line routes along the
energy corridor are not yet identified. It
is not feasible that all suitable habitat
for P. submutica will be avoided as the
corridor continues to be developed,
within the next 10 to 20 years.
The energy development activities
described above are occurring in close
proximity to Phacelia submutica
locations (WestWater Engineering 2004,
p. 11). Oil and gas pipelines, well pads,
and access roads are present on six P.
submutica sites within occurrences A,
D, E, and G (see Table 3 above; CNHP
2009g, records a, c, i, j, m, q). Frequently
travelled roads bisect and cross the
edges of occurrences A, D, and E. It is
likely that some of the seed bank was
displaced or destroyed to build the
roads and pipelines. On Federal lands,
direct impacts to known plant locations
are mostly being avoided by careful
placement of pipelines, well pads, and
associated facilities, due to the
candidate status of the species. Our
concern is primarily for the cumulative
impacts of energy development. When
all of the oil and gas wells are connected
to the system of local pipelines, roads,
and pumping stations, in combination
with cross-country transmission lines
and pipelines, more ROWs will be
necessary. Under these conditions, it is
difficult to protect occupied or potential
habitat for P. submutica. Blading of the
top few inches of soil during well pad
and road construction, installation of
underground pipelines, and
construction of associated buildings,
holding tanks, and other facilities alters
the unique soil structure and may
disturb, damage, or remove seed banks
that are critical to the survival of this
species. Any soil disturbance on
occupied habitat is likely to have a
deleterious effect on the in situ seed
bank and, therefore, on successful plant
recruitment and survival of the species
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35737
in subsequent years (Meyer et al. 2005,
p. 22).
Energy development increases access
to previously roadless areas, which
encourages ORV traffic to drive on
nearby slopes that support plant habitat.
ORV use occurs on BLM lands in the
general vicinity of Phacelia submutica
and is recorded within occupied habitat
at three sites within occurrences A and
I (seeSee Table 3 above) (CNHP 2009g,
records a, c, w; Mayo 2008d, photo).
The vehicles stray from designated
roads to climb hills for recreational
purposes. At a site in occurrence A, the
tracks from ORVs have disturbed most
of the habitat (Mayo 2008d, photo).
Substantial surface disturbance due to
churning by ORV tires can alter the
unique soil structure required by this
species, with the same negative effects
on the seed bank as described above.
Cattle trampling within occupied
habitat is documented at 5 sites within
occurrences B, F, and G (see Table 3
above; CNHP 2009g, records d, o, q, r,
t). The Ashmead Draw occurrence (C) is
severely trampled, with a poor viability
(D) rank (CNHP 2009g, records d–e).
Substantial surface disturbance, due to
heavy trampling by cattle, increases soil
compaction and erosion and alters the
microhabitat, such as the cracked soil
surface, the species requires.
Livestock-related impacts have
resulted in the loss of similar plant
species in other locations. A rare
ephemeral annual desert plant in Idaho
(comparable to P. submutica), with
highly specific soil requirements and
that depends on its seed bank, went
from thousands of plants in 1995 to no
new plants after intensive trampling by
cattle when the soil was wet and seeds
were germinating (Meyer et al. 2005, p.
22). The population has not recovered,
which is believed to be due to damage
and burying of seeds that prevented
them from germinating. After 11 years of
monitoring, researchers have clear
evidence that ‘‘any form of soil
disturbance is likely to have a
deleterious effect on the in situ seed
bank,’’ and that all potential habitat for
such a species (like P. submutica)
should be managed as if it were
currently occupied (Meyer et al. 2005,
p. 22).
Two water reservoir projects known
as Roan Creek and Sulphur Gulch have
been proposed in the past within
occupied habitat of Phacelia submutica.
The potential reservoir locations would
have impacted two sites within the
Sulphur Gulch 1 occurrence (I, u-v in
Table 3 above) and three sites within the
Logan Wash occurrence (D, f-g-h in
Table 3 above). Recently, both projects
were again evaluated as potential
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reservoirs to provide a water supply for
instream flows for endangered fishes in
the Colorado River (Friedel 2004, p. 1;
Grand River Consulting Corporation
2009, p. 3). After evaluation of
numerous alternatives, the Sulphur
Gulch and Roan Creek projects are no
longer being considered as an
alternative for a water supply for
endangered fishes (Bray and Drager
2008, pers. comm.; Grand River
Consulting Corporation 2009, pp. 1–5).
The Roan Creek reservoir project was
also proposed by Chevron Shale Oil
Company and Getty Oil Exploration
Company to be used for development of
oil shale extraction (Chevron-Getty
2002, pp. 2, 8). These potential
reservoirs could permanently destroy
plants and their habitat by project
construction and inundation. Since the
proposals have been withdrawn, these
threats are not imminent; however, the
sites have been identified as potential
reservoir locations that could be
developed within 20 years if warranted
by increased demands for water.
Increased demands are likely,
depending on the oil shale market,
urban development in Colorado, and
less precipitation due to climate change.
TABLE 4. THREATS TO Phacelia submutica HABITAT BY SOURCE AND OCCURRENCE. OCCURRENCES
A to X refer to Table 3 (CNHP 2009g, records a–hh, observation dates 1982 to 2008;
CNHP 2010, records ii, jj; WestWater Engineering 2007, pp. 16, 17, 19, 27; Ewing 2009, map).
Occurrence
A
B
Energy
X
WestWide
Corridor
X
X
Trampling
X
X
ORV
X
Roads
X
D
E
F
G
X
Reservoirs
C
X
X
X
X
X
X
X
X
X
X
I
X
M
N
O
P
Q
R
S
T
U
V
W
X
X
X
X
X
X
X
X
X
X
X
X
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Overutilization for commercial,
recreational, scientific, or educational
purposes is not known to be a threat to
Phacelia submutica. Therefore, we are
not addressing this factor in this
proposed rule.
C. Disease or Predation
Disease and herbivory are not known
to affect Phacelia submutica. Therefore,
15:05 Jun 22, 2010
L
X
X
We consider destruction, modification
and fragmentation of habitat to be
moderate threats to Phacelia submutica
throughout its range, due to ongoing
development of oil and gas with
associated pipelines, construction of
new road and utility ROWs, road
widening, and construction of access
roads. P. submutica habitat is also
threatened by soil modification
resulting from livestock trampling and
ORV tracking. These threats are of
moderate magnitude because they are
currently affecting at least 14 of the 25
occurrences, and because the plants and
their seed banks occur in small isolated
patches that are easily destroyed by
small-scale disturbances. If these threats
increase in frequency or severity, the
species is likely to become endangered
within the foreseeable future.
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X
No Data
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X
X
X
X
H
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X
X
X
we are not addressing this factor in this
proposed rule.
D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
Approximately 3 percent of Phacelia
submutica occupied habitat occurs on
private lands and another 12 percent on
a combination of private and BLM lands
(see Table 3 above). We are not aware
of any city or county ordinances or
zoning that provide for protection or
conservation of P. submutica or its
habitat on private lands.
State Laws and Regulations
No State regulations protect rare plant
species in Colorado. The CNAP has
entered into agreements with BLM to
help protect the Pyramid Rock
occurrence of Phacelia submutica, by
managing it as a Designated State
Natural Area that is monitored by
volunteer stewards. This management
agreement can be terminated with 90–
day written notice by either party.
Therefore, we have concluded that the
Designated Natural Area designation
alone does not constitute an adequate
regulatory mechanism to conserve P.
submutica.
Federal Laws and Regulations
Section 365 of the Energy Policy Act
of 2005 (42 U.S.C. 15801 et seq.)
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X
X
X
establishes a Federal Permit
Streamlining Pilot Project with the
intent to improve the efficiency of
processing oil and gas use
authorizations on Federal lands. The
two BLM pilot project offices for
Colorado are in the Glenwood Springs
and Grand Junction Field Offices, both
of which manage Phacelia submutica
habitat. Faster processing of permits to
drill increases the likelihood of ground
disturbance on P. submutica habitat
because the plants are ephemeral
annuals that can only be found for about
6 weeks during favorable years, and not
all suitable habitat has been surveyed.
When the plants are not present or
previously documented, avoidance of
the seed bank depends on field
assessments of suitable habitat. Suitable
habitat covers more area than the ‘‘sweet
spots’’ where the plants grow, and
suitable habitat has no regulatory
protection (BLM 2008d, p. 36). As a
result, seed banks and suitable habitat
are increasingly likely to be disturbed or
removed during the process of
approving locations for new energy
development projects.
Candidate species are managed by
BLM as sensitive species; BLM has a
policy for management of sensitive
species that recommends avoidance and
minimization of threats to plants and
habitat, as well as habitat conservation
assessments and conservation
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agreements (BLM 2008d, pp. 8, 36–38).
No assessments or agreements have
been formalized for Phacelia submutica.
As opposed to listed species, biological
assessments or consultation with the
Service are not required for BLMdesignated sensitive species during the
authorization process for oil and gas use
on Federal lands (BLM 2008d, p. 33).
Phacelia submutica is currently on
the sensitive species list for the USFS,
Region 2, which includes all USFS
lands in Colorado. The USFS manages
less than 10 percent of the suitable
habitat for P. submutica (Occurrence H,
CNHP 2009g, records q, r, s, t). A
proposed Lower Battlement Mesa
Research Natural Area to protect the
species on the White River National
Forest has not been formally established
(Ladyman 2003, pp. 8, 23; Proctor 2010,
pers. comm). If established, protection
would include restrictions on ORV use,
livestock grazing, and resource
extraction. Trampling of the habitat of P.
submutica by cattle has been observed
at three of the four occupied sites on
USFS land (CNHP 2009g, records q, r,
t).
The BLM policy of avoidance and
minimization of threats to plants and
habitatmay not adequately protect
Phacelia submutica because the plants
can only be found for a few weeks
during years when growing conditions
have been favorable (Burt and
Spackman 1995, p. 8). Thus, wellintentioned avoidance and
minimization measures may not be
implemented if no plants are seen even
in areas where subsequent timely
surveys would likely demonstrate a
persistent seed bank. Because available
inventories are not all recent, and
drilling permits are expedited, plant
occurrences, especially as seed banks,
may be overlooked in the permitting
process. The BLM attempts to avoid
disturbances that would adversely affect
sensitive species’ viability or trend the
species toward Federal listing. This
includes avoidance of suitable habitat if
it can be identified as such (BLM 2008d,
pp. 8, 36; BLM 2008e, pp. 5–7). In spite
of such efforts, pipeline ROWs exist
within 20 ft (6 m) and 100 ft (30 m) of
known P. submutica occurrences
(DeYoung 2009f, pers. comm.). We
recommend buffers of 656 ft (200m)
between the edge of disturbance and
suitable plant habitat to protect the
plants from destruction by vehicles that
stray outside of the project area, runoff,
erosion, dust deposition, or other
indirect effects such as destruction of
pollinator nesting habitat.
Five occurrences of Phacelia
submutica are located on BLM land in
an area called South Shale Ridge that
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covers more than a third of the known
range for this species (BLM 2005b, p. 5).
Part of South Shale Ridge was
recommended as an ACEC for
protection of P. submutica in 1995, but
was not designated as an ACEC (Burt
and Spackman 1995, p. 36) in that area.
Portions of South Shale Ridge that were
withheld from leasing in the past were
leased for oil and gas development in
November 2005 (BLM 2005b, p. 5).
These leases were subsequently deferred
pending development of a new Resource
Management Plan for the Grand
Junction Field Office (Ewing 2008c,
pers. comm.; BLM 2005b, p. 5). If the
BLM sells these leases, then 8 ac (3 ha)
of occupied P. submutica habitat within
about 65 ac (26 ha) of suitable habitat
will be newly opened to natural gas
development in a previously
undeveloped area (Ewing 2009, map).
Pyramid Rock is adjacent to South
Shale Ridge, and the Pyramid Rock
occurrence of Phacelia submutica is
within the BLM Pyramid Rock ACEC,
including an estimated 31 to 2,055
plants (depending on the year) within
20 occupied ac (8 ha) on 160 ac (64.7
ha) of suitable habitat (CNHP 2009g,
record c; Wenger 2009, pp. 1-11). The
ACEC designation carries no protection
in and of itself (BLM 2006, pp. 2–65).
Stipulations of no new surface
occupancy or ground disturbance apply
to this ACEC for protection of candidate,
proposed, and listed plant species.
However, due to the possibility of
exceptions being granted, we cannot
predict with any degree of certainty
what stipulations will actually be
applied to the plant or its habitat that
ensure the long term conservation of the
species. BLM installed cable fence in
2007 to deter ORVs from crossing
habitat for a federally threatened cactus
(Sclerocactus glaucus, Colorado
hookless cactus) and P. submutica. The
BLM excluded this ACEC from a South
Shale Ridge lease sale in 2005 (CNHP
2005, p. 5; BLM 2005b, p. 5). P.
submutica plants have not been directly
impacted since the fence was installed,
and existing pipeline and roads remain
outside the fence. The ACEC has
provided adequate protection thus far
for about 5 percent of the known
occupied habitat for the species (CNHP
2009g, record c).
No adequate regulatory mechanisms
currently exist to protect Phacelia
submutica. We consider the inadequacy
of existing regulatory mechanisms to be
a significant and ongoing threat to P.
submutica because no formal plans or
agreements beyond one ACEC are in
place to protect this plant. Sensitive
species designations provide policies to
be carried out with the resources
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35739
available, but they do not provide
regulations to protect this species from
losing habitat and seed banks to energy
development projects, cattle trampling,
or ORV traffic over the next 10 to 20
years. Therefore, this plant is likely to
become endangered within the
foreseeable future.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Climate change is likely to affect
Phacelia submutica because seed
germination, seed dormancy, and
persistence of the seed bank are all
directly dependent on precipitation and
temperature patterns (Levine et al. 2008,
p. 805). As described above, climate
modeling is not currently to the level
that we can predict the amount of
temperature and precipitation change
within the limited range of P.
submutica. Therefore, this discussion
generally addresses what could happen
under the current climate predictions.
However, we need further refinement of
the current predictions to draw more
reliable conclusions concerning the
effects of climate change on the species.
Localized projections suggest the
Southwest, including Colorado, may
experience the greatest temperature
increase of any area in the lower 48
States (IPCC 2007, p. 30). It is very
likely that hot extremes, heat waves,
and heavy precipitation will increase in
frequency (IPCC 2007, p. 46). A 10- to
30-percent decrease in runoff in midlatitude western North America is
projected by the year 2050 based on an
ensemble of 12 climate models (Milly et
al. 2005, p. 1).
Future changes in the timing of the
first major spring rains each year, and
temperatures associated with the first
major spring rains each year may more
strongly affect germination and
persistence of ephemeral annual plants
than changes in season-long rainfall
(barring severe droughts) (Levine et al.
2008, p. 805). Increasing environmental
variance might decrease extinction risk
for rare desert ephemeral plants,
because these plants typically rely on
extremely good years to restock the
persistent seed bank while extremely
bad years have little impact (Meyer et al.
2006, p. 901). However, extremely long
droughts resulting from climate change,
with no good years for replenishing the
seed bank, would likely cause Phacelia
submutica to become endangered. A
persistent seed bank enables the species
to survive drought. However, because
the soil can remain bare of P. submutica
plants for several years, it is difficult to
identify and protect the seemingly
unoccupied habitat that occurs in small,
isolated patches that are easily
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destroyed by small-scale disturbances,
and can be overlooked during habitat
assessments. The longer the species
remains dormant, the less likely it is
that we will know if an area is occupied,
reducing our ability to avoid impacts to
the species and protect it from becoming
endangered.
While current climate change
predictions are not reliable enough at
the local level for us to draw
conclusions about its effects on P.
submutica, it is likely that there will be
drying trends in the future and the seeds
will remain dormant for long periods.
This would make it increasingly
difficult to detect occupied habitat and
avoid destruction of habitat and more
likely that the species will become
endangered.
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Proposed Determination
We have carefully assessed the best
scientific and commercial information
available regarding past, present, and
future threats to Ipomopsis polyantha,
Penstemon debilis, and Phacelia
submutica. Section 3(6) of the Act
defines an endangered species as ‘‘any
species which is in danger of extinction
throughout all or a significant portion of
its range,’’ and section 3(20) defines a
threatened species as ‘‘any species
which is likely to become an
endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ 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. Each of the three endemic
plant species proposed for listing in this
rule is highly restricted in its range and
the threats occur throughout its range.
Therefore, we assessed the status of
each species throughout its entire range.
In each case, the threats to the survival
of these species occur throughout the
species’ range and are not restricted to
any particular significant portion of that
range. Accordingly, our assessment and
proposed determination applies to each
species throughout its entire range. Our
proposed determination for each species
is presented below.
Ipomopsis polyantha
The species’ highly restricted soil
requirements and geographic range
make it particularly susceptible to
extinction at any time due to
commercial, municipal, and residential
development; associated road and
utility improvements and maintenance;
heavy livestock use; inadequacy of
existing regulatory mechanisms;
fragmented habitat; and prolonged
drought (see Factors A, C, D, and E).
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The main occurrence of Ipomopsis
polyantha includes 3 mi (4.8 km) of
highway ROW and the private
properties that extend 0.25 to 1.2 mi (0.4
to 1.9 km) on either side of the highway.
A smaller occurrence of about 23 ac (9
ha) includes highway ROWs, private
land, and 20 ac (8 ha) of BLM land. The
loss or fragmentation of either
occurrence would represent a
substantial loss to the viability of the
species. Both known occurrences face
ongoing, new, and potential threats,
including commercial, residential and
municipal development; associated road
and utility improvements and
maintenance; heavy livestock use;
inadequacy of existing regulatory
mechanisms; fragmented habitat; and
prolonged drought conditions. The level
of threat for I. polyantha is high due to
the direct overlap of rapid land
development on 91 percent of the
known suitable habitat. The County and
Town Community Plan includes high to
low density development over the
species’ entire range. Private
landowners are considering commercial
and residential development that would
include a parcel at the intersection of
US 160 and US 84 that currently
contains the highest density of plants.
Planned development will transform
the land adjacent to US 84, at the center
of the species’ distribution, from lowdensity residential/agricultural land use
to commercial, townhome, and higher
density residential use. The cumulative
impact of current and planned
development could result in extensive
disturbance and destruction of the
remaining habitat within the next 5 to
10 years, putting the species in danger
of extinction.
On the basis of the best available
information, we propose to list
Ipomopsis polyantha as an endangered
species. Endangered status reflects the
vulnerability of this species to threat
factors negatively affecting it and its
limited and restricted habitat. I.
polyantha is in danger of extinction
throughout all of its range.
Penstemon debilis
Extremely low numbers and a highly
restricted geographic range make
Penstemon debilis particularly
susceptible to becoming endangered in
the foreseeable future. Threats to the
species and its habitat include energy
development, road maintenance,
inadequacy of existing regulatory
mechanisms, and stochastic events (see
Factors A, D, and E).
The total estimated number of plants
in the 4 viable occurrences is about
4,000 individuals. It is likely that
additional unknown occurrences exist
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(Spackman-Panjabi 2008, pers. comm.).
Three of the 4 viable occurrences are on
lands owned by an energy development
company. The energy development
company has pledged to manage
development to minimize impacts to the
plants; however, the agreement is not
legally binding. The fourth occurrence,
on BLM land, is subject to disturbance
as a result of the ongoing CERCLA
project and road maintenance. The loss
of any one occurrence would represent
a substantial diminution in the viability
of the species. All four known
occurrences face ongoing or potential
threats, including oil and gas
development, oil shale mining and
associated impacts, road maintenance,
inadequacy of existing regulatory
mechanisms, and potential stochastic
events. The level of threats this poses
for Penstemon debilis is considered high
due to the direct overlap of energy
resources and all known species
occurrences. The BLM RFD scenario
predicts extensive gas development
within or near the species’ range within
the foreseeable future (BLM 2005b, pp.
4–11). The BLM RFD, in conjunction
with the stated intention of the owner
of the land containing the majority of
the plants to develop natural gas in the
vicinity of the plant occurrences, could
result in disturbance to the remaining
occurrences within the next 20 years,
resulting in the species being likely to
become endangered.
The primary factors threatening
Penstemon debilis are: the present or
threatened destruction, modification or
curtailment of P. debilis habitat and
range; and the inadequacy of existing
regulatory mechanisms. These factors
pose immediate threats to the species
because they have been ongoing.
However, these threats are moderate in
severity because actual impacts to
individual plants and occupied habitat
as a result have been, and are expected
to be limited, and the species is able to
slowly recover and recolonize after
disturbance. Therefore, on the basis of
the best available information, we
propose to list P. debilis as a threatened
species. Threatened status reflects the
vulnerability of this species to factors
that negatively affect the species and its
limited and restricted habitat.
Penstemon debilis is likely to become
endangered in the foreseeable future if
present threats increase.
Phacelia submutica
The current range of Phacelia
submutica is subject to human-caused
modifications from natural gas
exploration and production with
associated expansion of pipelines,
roads, and utilities; development within
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the Westwide Energy Corridor;
increased access to the habitat by ORVs;
soil and seed disturbance by cattle
(Factor A); and inadequate regulations
(Factor D). The species’ small
geographic range, highly specific soil
and germination requirements, limited
seed dispersal, fragmented habitat,
prolonged seed dormancy, and potential
seed bank depletion by prolonged
drought (Factor E) make P. submutica
vulnerable to these threats to an extent
that the species may become
endangered within the foreseeable
future (10 to 20 years), depending
primarily on the rate of future energy
development.
Phacelia submutica occurs on about
104 ac (42 ha) of known occupied
habitat (see Table 3 above) (CNHP
2009g, records a–hh; CNHP 2010,
records ii–jj; WestWater Engineering
2007, pp. 16, 17, 19, 27). All known
occurrences are in the midst of the third
largest natural gas-producing area in
Colorado (COGCC 2008, p. 1). Based on
the rate of current and proposed energy
development over the entire range of the
species (COGCC 2008 p. 1; COGCC 2009
p. 1; Ewing 2009, map), we estimate that
at least 50 percent of the known habitat
has the potential to be modified or
destroyed within 10 to 20 years, thus
making it likely that the species will
become endangered within that time.
The plants and their seed banks occur
in small, isolated patches that are easily
destroyed by small-scale disturbances.
In the past 20 years, we have found
three new occurrences, but no
expansion of the known range of the
species (CNHPg 2009, a–hh; CNHP
2010, records ii–jj; WestWater
Engineering 2007, pp. 16, 17, 19, 27).
Numbers of flowering plants fluctuate,
but they do not disperse seeds beyond
the existing patches of unique soil that
are separated from one another by a few
yards or several miles (Ewing 2008b,
map). Any loss of occupied habitat will
be a permanent loss for the foreseeable
future, and cause a decline in the status
of the species.
On the basis of the best available
information, we propose to list Phacelia
submutica as a threatened species.
Threatened status reflects the
vulnerability of this species to factors
that negatively affect the species and its
limited and restricted habitat. While not
in immediate danger of extinction, P.
submutica has the strong potential to
become an endangered species in the
foreseeable future if habitat is lost and
existing seed banks cannot expand to
maintain the species’ range.
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Available Conservation Measures
Conservation tools provided by the
Service’s Candidate Conservation
Program are available for these three
species. Our Candidate Conservation
Program assesses species and develops
and facilitates the use of voluntary
conservation tools for collaborative
conservation of candidate and other
species-at-risk and their habitats, so that
they do not need the protection of the
Act. Candidate Conservation
Agreements (CCAs) could provide
adequate regulatory mechanisms for
these three species if such agreements
could be finalized by the time of our
final listing determination. The CCAs
are voluntary conservation agreements
between the Service and one or more
public or private parties that identify
threats to candidate species, plan
actions to address threats and conserve
the species, and implement
conservation measures.
Because the three species are
narrowly distributed on lands owned by
a relatively small number of
landowners, we believe that the
development of CCAs with the BLM and
with private entities and State and local
agencies could be effective in
addressing the threats. We are open to
working with any landowners on
developing such plans to assure the
conservation of these species. Any such
agreement finalized before our listing
decision will be evaluated according to
our Policy on Evaluating Conservation
Efforts When Making Listing Decisions
(68 FR 15100, March 28, 2003) to
determine if the agreement constitutes
an adequate regulatory mechanism.
Conservation measures provided to
species listed as endangered or
threatened 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, 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 measures
required of 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
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35741
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. The recovery plan identifies sitespecific 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
(comprised of species experts, Federal
and State agencies, non-government
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 website (https://www.fws.gov/
endangered), or from our Western
Colorado Ecological Services Field
Office (see FOR FURTHER INFORMATION
CONTACT).
Implementation of recovery actions
generally requires the participation of a
broad range of partners, including other
Federal agencies, States, 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.
Achieving recovery of these species
requires cooperative conservation efforts
on private and public lands.
If these three plant 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 nonFederal landowners, the academic
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community, and nongovernmental
organizations. In addition, under section
6 of the Act, the State of Colorado
would be eligible for Federal funds to
implement management actions that
promote the protection and recovery of
Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica.
Information on our grant programs that
are available to aid species recovery can
be found at: https://www.fws.gov/grants.
Although Ipomopsis polyantha,
Penstemon debilis, and Phacelia
submutica are only proposed for listing
under the Act at this time, please let us
know if you are interested in
participating in recovery efforts for
these species. Additionally, we invite
you to submit any new information on
these species whenever it becomes
available and any information you may
have for recovery planning purposes to
the person listed under 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
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed, 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 formal consultation with the
Service.
Federal agency actions within the
habitat of these species that may require
conference or consultation or both, as
described in the preceding paragraph,
include the following for each species:
Ipomopsis polyantha—Permitting of
grazing and authorization of utility or
access ROWs by the BLM. Other types
of actions that may require consultation
include provision of Federal funds to
State and private entities through
Federal programs, such as Colorado
Department of Transportation highway
construction or improvement projects,
Housing and Urban Development Tax
Credit Assistance Program, the Service’s
Landowner Incentive Program, and
various grants administered by the U.S.
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Department of Agriculture and Natural
Resources Conservation Service (USDANRCS)
Penstemon debilis—Oil and gas
leasing, exploration, and permitting; oil
shale research; authorization of
transmission towers, pipelines and
power lines; reclamation actions; travel
management; and authorization of road
maintenance by the BLM. Other types of
actions that may require consultation
include provision of Federal funds to
State and private entities through
Federal programs, such as the Service’s
Landowner Incentive Program, State
Wildlife Grant Program, and Federal
Aid in Wildlife Restoration program, as
well as the various grants administered
by USDA-NRCS.
Phacelia submutica—Oil and gas
leasing, exploration, permitting,
development, pipelines and
transmission lines; permitting of
grazing; authorization of travel routes;
road construction or maintenance by the
BLM or the USFS; and authorization of
pipeline and power line routes within
the Westwide Energy Corridor. Other
types of actions that may require
consultation include water reservoir
construction and provision of Federal
funds to State and private entities
through Federal programs, such as the
Service’s Landowner Incentive Program,
and various grants administered by
USDA-NRCS.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to threatened and endangered plants.
All prohibitions of section 9(a)(2) of the
Act, implemented by 50 CFR 17.61 and
50 CFR 17.71, apply. 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, damaging,
or destroying of such plants in knowing
violation of any State law or regulation,
including State criminal trespass law.
Certain exceptions to the prohibitions
apply to agents of the Service and State
conservation agencies. Colorado’s
Endangered Species law does not
currently cover plants and does not
provide protection to Ipomopsis
polyantha, Penstemon debilis, and
Phacelia submutica. Therefore, listing
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under the Act will offer additional
protection to these species.
The Act, 50 CFR 17.62, and 50 CFR
17.72 also provide for the issuance of
permits to carry out otherwise
prohibited activities involving
endangered and threatened plants under
certain circumstances. Such permits are
available for scientific purposes and to
enhance the propagation or survival of
the species. We anticipate that the only
permits that would be sought or issued
for Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica would
be in association with research and
recovery efforts, as these species are not
common in cultivation or in the wild.
Requests for copies of the regulations
regarding listed species and inquiries
about prohibitions and permits may be
addressed to U.S. Fish and Wildlife
Service, Ecological Services, P.O. Box
25486 - DFC, Denver, CO 80225-0486
(telephone 303-236-4256; facsimile 303236-0027).
Critical Habitat
Background
Critical habitat is defined in section
3(5)(A) of the Act as:
(i) The specific areas within the
geographical area occupied by the
species, at the time it is listed in
accordance with the Act, on which are
found those physical or biological
features
(I) essential to the conservation of the
species and
(II) which may require special
management considerations or
protection; and
(ii) specific areas outside the
geographical area occupied by the
species at the time it is listed, upon a
determination that such areas are
essential for the conservation of the
species.
Conservation, as defined under
section 3(3) of the Act, means to use and
the use of all methods and procedures
that are necessary to bring an
endangered or threatened species to the
point at which the measures provided
under the Act are no longer necessary.
Such methods and procedures include,
but are not limited to, all activities
associated with scientific resources
management such as research, census,
law enforcement, habitat acquisition
and maintenance, propagation, and
transplantation.
Critical habitat receives protection
under section 7 of the Act through the
prohibition against Federal agencies
carrying out, funding, or authorizing the
destruction or adverse modification of
critical habitat. Section 7(a)(2) requires
consultation on Federal actions that
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may affect critical habitat. The
designation of critical habitat does not
affect land ownership or establish a
refuge, wilderness, reserve, preserve, or
other conservation area. Such
designation does not allow the
government or public to access private
lands. Such designation does not
require implementation of restoration,
recovery, or enhancement measures by
non-Federal landowners. Where a
landowner seeks or requests Federal
agency funding or authorization for an
action that may affect a listed species or
critical habitat, the consultation
requirements of section 7(a)(2) of the
Act would apply, but even in the event
of a destruction or adverse modification
finding, the Federal action agency’s and
the applicant’s obligation is not to
restore or recover the species, but to
implement reasonable and prudent
alternatives to avoid destruction or
adverse modification of critical habitat.
For inclusion in a critical habitat
designation, the habitat within the
geographical area occupied by the
species at the time it was listed must
contain the physical and biological
features essential to the conservation of
the species, and be included only if
those features may require special
management considerations or
protection. Critical habitat designations
identify, to the extent known using the
best scientific and commercial data
available, habitat areas that provide
essential life cycle needs of the species
(areas on which are found the physical
and biological features laid out in the
appropriate quantity and spatial
arrangement for the conservation of the
species). Under the Act and regulations
at 50 CFR 424.12, we can designate
critical habitat in areas outside the
geographical area occupied by the
species at the time it is listed only when
we determine that those areas are
essential for the conservation of the
species and that designation limited to
those areas occupied at the time of
listing would be inadequate to ensure
the conservation of the species.
Section 4 of the Act requires that we
designate critical habitat on the basis of
the best scientific, commercial, and
economic data available. Further, our
Policy on Information Standards under
the Act (published in the Federal
Register on July 1, 1994 (59 FR 34271)),
the Information Quality Act (section 515
of the Treasury and General
Government Appropriations Act for
Fiscal Year 2001 (Pub. L. 106-554; H.R.
5658)), and our associated Information
Quality Guidelines, provide criteria,
establish procedures, and provide
guidance to ensure that our decisions
are based on the best scientific data
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available. They require our biologists, to
the extent consistent with the Act and
with the use of the best scientific data
available, to use primary and original
sources of information as the basis for
recommendations to designate critical
habitat.
When we determine which areas
should be designated as critical habitat,
our primary source of information is
generally the information developed
during the listing process for the
species. Additional information sources
may include the recovery plan for the
species, articles in peer-reviewed
journals, conservation plans developed
by States and counties, scientific status
surveys and studies, biological
assessments, or other unpublished
materials and expert opinion or
personal knowledge.
Habitat is often dynamic, and species
may move from one area to another over
time. Furthermore, we recognize that
critical habitat designated at a particular
point in time may not include all of the
habitat areas that we may later
determine are necessary for the recovery
of the species. For these reasons, a
critical habitat designation does not
signal that habitat outside the
designated area is unimportant or may
not be required for recovery of the
species.
Areas that are important to the
conservation of the species, but are
outside the critical habitat designation,
will continue to be subject to
conservation actions we implement
under section 7(a)(1) of the Act. Areas
that support occurrences also are subject
to the regulatory protections afforded by
the section 7(a)(2) jeopardy standard, as
determined on the basis of the best
available scientific information at the
time of the agency action. Federally
funded or permitted projects affecting
listed species outside their designated
critical habitat areas may still result in
jeopardy findings in some cases.
Similarly, critical habitat designations
made on the basis of the best available
information at the time of designation
will not control the direction and
substance of future recovery plans,
habitat conservation plans, or other
species conservation planning efforts if
new information available at the time of
these planning efforts calls for a
different outcome.
Prudency Determination
Section 4(a)(3) of the Act, as
amended, and implementing regulations
(50 CFR 424.12) require that, to the
maximum extent prudent and
determinable, the Secretary designate
critical habitat at the time the species is
determined to be endangered or
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threatened. Our regulations (50 CFR
424.12(a)(1)) state that the designation
of critical habitat is not prudent when
one or both of the following situations
exist: (1) The species is threatened by
taking or other human activity, and
identification of critical habitat can be
expected to increase the degree of threat
to the species, or (2) such designation of
critical habitat would not be beneficial
to the species.
There is no documentation that
Ipomopsis polyantha, Penstemon
debilis, or Phacelia submutica are
threatened by collection or other
intentional taking. In the absence of
finding that the designation of critical
habitat would increase threats to a
species, if there are any benefits to a
critical habitat designation, then a
designation is prudent. The potential
benefits include: (1) Triggering
consultation under section 7 of the Act,
in new areas for actions in which there
may be a Federal nexus where it would
not otherwise occur because, for
example, it is or has become
unoccupied or the occupancy is in
question; (2) focusing conservation
activities on the most essential features
and areas; (3) providing educational
benefits to State or county governments
or private entities; and (4) preventing
people from causing inadvertent harm
to the species because they do not know
it may be present.
The primary regulatory effect of
critical habitat is the section 7(a)(2)
requirement that Federal agencies
refrain from taking any action that
destroys or adversely affects critical
habitat. At present, the only known
extant individuals of Ipomopsis
polyantha occur on private, town,
county, and BLM lands, and on Federal
highway ROWs. Most of the known
individuals of Penstemon debilis occur
on private land; however,
approximately 18 percent of the
individuals occur on Federal lands.
Approximately 3 percent of known
occupied habitat for Phacelia submutica
occurs on private lands and another 12
percent on a combination of private and
BLM lands, with the remaining 85
percent occurring on BLM and USFS
lands. Lands that may be designated as
critical habitat for these species in the
future may be subject to Federal actions
that trigger the section 7 consultation
requirement. All projects taking place
on Federal lands that may affect critical
habitat would require consultation.
Projects on private land would require
consultation if they include a Federal
action, such as the granting of Federal
monies for conservation projects or the
need for Federal permits for projects.
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There also may be some educational
or informational benefits to the
designation of critical habitat.
Educational benefits include the
notification of landowners, land
managers, and the general public of the
importance of protecting the habitat of
this species. In the case of I. polyantha,
P. debilis, and P. submutica, these
aspects of critical habitat designation
would potentially benefit the
conservation of these species. Therefore,
because we have determined that the
designation of critical habitat will not
likely increase the degree of threat to
these species and may provide some
measure of benefit, we find that
designation of critical habitat is prudent
for I. polyantha, P. debilis, and P.
submutica.
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Critical Habitat Determinability
As stated above, section 4(a)(3) of the
Act requires the designation of critical
habitat concurrently with the species’
listing ‘‘to the maximum extent prudent
and determinable.’’ Our regulations at 50
CFR 424.12(a)(2) state that critical
habitat is not determinable when one or
both of the following situations exist:
(i) Information sufficient to perform
required analyses of the impacts of the
designation is lacking, or
(ii) The biological needs of the species
are not sufficiently well known to
permit identification of an area as
critical habitat.
When critical habitat is not
determinable, the Act provides for an
additional year to publish a critical
habitat designation (16 U.S.C.
1533(b)(6)(C)(ii)).
In accordance with section 3(5)(A)(i)
and 4(b)(1)(A) of the Act and the
regulations at 50 CFR 424.12, in
determining which areas occupied by
the species at the time of listing to
designate as critical habitat, we consider
the physical and biological features
essential to the conservation of the
species which may require special
management considerations or
protection. These include, but are not
limited to:
(1) Space for individual and
population growth and for normal
behavior;
(2) Food, water, air, light, minerals, or
other nutritional or physiological
requirements;
(3) Cover or shelter;
(4) Sites for breeding, reproduction,
and rearing (or development) of
offspring; and
(5) Habitats that are protected from
disturbance or are representative of the
historical geographical and ecological
distributions of a species.
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We are currently unable to identify
the essential physical and biological
features for Ipomopsis polyantha,
Penstemon debilis, and Phacelia
submutica, because information on the
physical and biological features that are
considered essential to the conservation
of these species is not sufficiently
known at this time. Explanations for
each species follow:
Ipomopsis polyantha—As discussed
in the ‘‘Species Information’’ section of
this proposed rule, the historical range
of the species is unknown, and access
to potential habitat on private land is
restricted. The role of disturbance in the
species’ spread and persistence is
currently unknown. Our ability to
translocate the species is limited at this
time. Key features of the plant’s life
history, such as longevity, dispersal
mechanisms, or vectors for pollination,
are not entirely known. Much of the
plant community where the remaining
individuals of I. polyantha are found
has been highly modified by the
presence of grazing livestock and road
maintenance activities. The poor
viability of species’ occurrences
observed in recent years indicates that
current conditions are not sufficient to
meet the basic biological requirements
of this species. Although we can
surmise that habitat degradation from
threats described under Factor A above
has contributed to the decline of the
species, we do not know specifically
what essential physical or biological
features of that habitat are currently
lacking for I. polyantha. Because we are
unable to identify the physical and
biological features essential to the
conservation of I. polyantha, we are
unable to identify areas that contain
these features.
Penstemon debilis—Although we
know the specific elevation, soil and
geology types to which this species is
restricted, there is much more suitable
habitat in Western Colorado than that
known to be occupied by P. debilis.
Further scientific studies are needed to
determine the specific factors, unique to
the occupied habitat, to better determine
habitats suitable for designation as
critical habitat.
Phacelia submutica—Specific
components of occupied versus nonoccupied sites and soils have not been
analyzed for the Atwell Gulch and Shire
members of the Wasatch Formation
where the species occurs. Key features
of the plant’s life history, such as
longevity of the seed bank, dispersal
mechanisms, or vectors for pollination,
are unknown. Pollinator requirements
for habitat or alternate hosts have not
been identified. Because we are unable
to identify the physical and biological
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features essential to the conservation of
P. submutica, we are unable to identify
areas that contain these features.
Although we have determined that
the designation of critical habitat is
prudent for Ipomopsis polyantha,
Penstemon debilis, and Phacelia
submutica, the biological needs of these
species are not sufficiently well known
to identify the physical and biological
features that may be essential for the
conservation of these species, or those
areas essential to the conservation of
these species. Additionally, we have not
gathered sufficient economic and other
data on the impacts of a critical habitat
designation. These factors must be
considered as part of a designation
procedure. Therefore, we find that
critical habitat for I. polyantha, P.
debilis, and P. submutica is not
determinable at this time. We intend to
continue gathering information
regarding the essential life-history
requirements of these species to
facilitate identification of essential
features and areas. Field research in
2010 will increase our understanding of
pollinator needs and soil characteristics
for P. submutica, of development status
in I. polyantha habitat, and of the
habitat for the new occurrence of P.
debilis found in 2009. We will evaluate
the needs of I. polyantha, P. debilis, and
P. submutica within the ecological
context of the broader ecosystems in
which they occur, similar to the
approach that we recently used in our
final designation of critical habitat for
47 species endemic to the island of
Kauai (October 21, 2008; 73 FR 62592),
and will consider the utility of using
this approach for these species as well.
Peer Review
In accordance with our joint policy
published in the Federal Register on
July 1, 1994 (59 FR 34270), we will seek
the expert opinions of at least three
appropriate and independent specialists
regarding this proposed rule. The
purpose of peer review is to ensure that
our determination of status for these
species is based on scientifically sound
data, assumptions, and analyses. We
will invite these peer reviewers to
comment, during the public comment
period, on the specific assumptions and
conclusions regarding the proposal to
list Ipomopsis polyantha as endangered
and Penstemon debilis and Phacelia
submutica as threatened, and our
proposed determination regarding
critical habitat for these species. We will
send copies of this proposed rule to the
peer reviewers immediately following
publication in the Federal Register.
We will consider all comments and
information we receive during the
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comment period on this proposed rule
during preparation of a final
rulemaking. Accordingly, the final
decision may differ from this proposal.
Public Hearings
The Act provides for one or more
public hearings on this proposal, if
requested. Requests must be received
within 45 days after the date of
publication of this proposal in the
Federal Register. Such requests must be
sent to the address shown in the FOR
FURTHER INFORMATION CONTACT section.
We will schedule one or more public
hearings on this proposal, if any are
requested, and announce the dates,
times, and places of those hearings, as
well as how to obtain reasonable
accommodations, in the Federal
Register and local newspapers at least
15 days before the hearing(s).
Persons needing reasonable
accommodations to attend and
participate in a public hearing should
contact the Western Colorado Ecological
Services Field Office at 970-243-2778, as
soon as possible. To allow sufficient
time to process requests, please call no
later than 1 week before the hearing
date. Information regarding this
proposed rule is available in alternative
formats upon request.
Required Determinations
Clarity of the Rule
Executive Order 12866 requires each
agency to write regulations that are easy
to understand. We invite your
comments on how to make this rule
easier to understand including answers
to questions such as the following: (1)
Are the requirements in the rule clearly
stated? (2) Does the rule contain
technical language or jargon that
interferes with its clarity? (3) Does the
format of the rule (grouping and order
of sections, use of headings,
paragraphing, etc.) aid or reduce its
clarity? (4) Would the rule be easier to
understand if it were divided into more
(but shorter) sections? (5) Is the
description of the rule in the
SUPPLEMENTARY INFORMATION section of
the preamble helpful in understanding
the emergency rule? What else could we
do to make the rule easier to
understand?
Send a copy of any comments that
concern how we could make this rule
easier to understand to Office of
Regulatory Affairs, Department of the
Interior, Room 7229, 1849 C Street,
NW., Washington, D.C. 20240. You also
may e-mail the comments to this
address: Exsec@ios.goi.gov.
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.)
This proposed rule does not contain
any new collections of information that
require approval by Office of
Management and Budget (OMB) under
the Paperwork Reduction Act. This rule
would not impose new recordkeeping or
reporting requirements on State or local
governments, individuals, businesses, or
organizations. We may not conduct or
sponsor and you are not required to
respond to a collection of information
unless it displays a currently valid OMB
control number.
National Environmental Policy Act
We have determined that
Environmental Assessments and
Environmental Impact Statements, as
defined under the authority of the
National Environmental Policy Act of
1969 (42 U.S.C. 4321 et seq.), need not
be prepared in connection with
regulations adopted under section 4(a)
of the 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 all references cited
in this proposed rule is available on the
Internet at https://www.regulations.gov
or upon request from the Field
Supervisor, Western Colorado
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT section).
Author(s)
The primary authors of this document
are staff members of the Western
Colorado Ecological Services Field
Office (see FOR FURTHER INFORMATION
CONTACT section).
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Proposed Regulation Promulgation
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
50 of the Code of Federal Regulations,
as set forth below:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 16 U.S.C.
1531-1544; 16 U.S.C. 4201-4245; Pub. L. 99625, 100 Stat. 3500; unless otherwise noted.
2. In § 17.12(h) add entries for
Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica, in
alphabetical order under FLOWERING
PLANTS, to the List of Endangered and
Threatened Plants, as follows:
§ 17.12
plants.
*
Endangered and threatened
*
*
(h) * * *
*
*
Species
Historic range
Scientific name
Family
Status
When listed
Critical habitat
Special rules
Common name
FLOWERING PLANTS
*
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Species
Historic range
Scientific name
Phacelia
submutica
DeBeque phacelia
*
*
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U.S.A. (CO)
*
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[FR Doc. 2010–15251 Filed 6–22–10; 8:45 am]
BILLING CODE 4310–55–S
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R9-ES-2009-0094]
[MO92210-0-0010-B6]
Endangered and Threatened Wildlife
and Plants; 90-Day Finding on a
Petition to List the Honduran Emerald
Hummingbird as Endangered
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Notice of 90–day petition
finding and initiation of status review.
erowe on DSK5CLS3C1PROD with PROPOSALS-1
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), announce a
90–day finding on a petition to list as
endangered under the Endangered
Species Act of 1973, as amended (Act),
the Honduran emerald hummingbird
(Amazilia luciae). We find that the
petition presents substantial scientific
or commercial information indicating
that listing the Honduran emerald
hummingbird may be warranted.
Therefore, with the publication of this
notice, we are initiating a status review
of the Honduran emerald hummingbird
to determine if listing is warranted. To
ensure that the status review is
comprehensive, we are soliciting
information and data regarding this
species.
DATES: To allow us adequate time to
conduct this review, we request that we
receive information on or before August
23, 2010. After this date, you must
submit information directly to the
address in the FOR FURTHER INFORMATION
CONTACT section). Please note that we
may not be able to address or
incorporate information that we receive
after the above requested date.
ADDRESSES: You may submit comments
by one of the following methods:
15:05 Jun 22, 2010
Hydrophyllaceae
*
Dated: June 8, 2010
Jeffrey L. Underwood,
Acting Director, U.S. Fish and Wildlife
Service.
VerDate Mar<15>2010
Family
Status
When listed
Critical habitat
Special rules
Common name
Jkt 220001
*
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NA
*
• Electronically: Go to the Federal
eRulemaking Portal: https://
www.regulations.gov. In the Keyword
box, enter Docket No. FWS-R9-ES-20090094 which is the docket number for
this rulemaking. Then, in the Search
panel on the left side of the screen
under the Document Type heading,
click on the Proposed Rules link to
locate this document. You may submit
a comment by clicking on ‘‘Send a
Comment or Submission.’’
• By hard copy: Submit by U.S. mail
or hand-delivery to: Public Comments
Processing, Attn: FWS-R9-ES-20090094; Division of Policy and Directives
Management; U.S. Fish and Wildlife
Service; 4401 N. Fairfax Drive, Suite
222; Arlington, VA 22203.
We will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see the
Information Solicited section below for
more details).
FOR FURTHER INFORMATION CONTACT:
Nicole Alt, Chief, Division of
Conservation and Classification,
Endangered Species Program, U.S. Fish
and Wildlife Service, 4401 N. Fairfax
Drive, Room 420, Arlington, VA 22203;
telephone 703-358-2171; facsimile 703358-1735. If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Request for Information
When we make a finding that
substantial information is presented to
indicate that listing a species may be
warranted, we are required to promptly
review the status of the species (status
review). To ensure that the status review
is complete and based on the best
available scientific and commercial
information, we request information on
the Honduran emerald hummingbird.
We request scientific and commercial
information from the public, concerned
governmental agencies, the scientific
community, industry, or any other
interested parties on the status of the
Honduran emerald hummingbird,
throughout its range, including but not
limited to:
(1) Information on taxonomy,
distribution, habitat selection and
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trends (especially breeding and foraging
habitats), diet, and population
abundance and trends (especially
current recruitment data) of this species.
(2) Information on the effects of
habitat loss and changing land uses on
the distribution and abundance of this
species and its principal food sources
over the short and long term.
(3) Information on whether changing
climatic conditions are affecting the
species, its habitat, or its prey base.
(4) Information on the effects of other
potential threat factors, including live
capture and collection, domestic and
international trade, predation by other
animals, and diseases of this species or
its principal food sources over the short
and long term.
(5) Information on management
programs for hummingbird
conservation, including mitigation
measures related to conservation
programs, and any other private, tribal,
or governmental conservation programs
that benefit this species.
(6) Information relevant to whether
any populations of this species may
qualify as distinct population segments.
(7) Information on captive
populations and captive breeding and
domestic trade of this species in the
United States
(8) Genetics and taxonomy;
(9) The factors that are the basis for
making a listing determination for a
species under section 4(a) of the Act (16
U.S.C. 1531 et seq.), which are:
(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.
Please include sufficient information
with your submission (such as full
references) to allow us to verify any
scientific or commercial information
you include.
We will base our status review on the
best scientific and commercial
information available, including all
information we receive during the
public comment period. Please note that
E:\FR\FM\23JNP1.SGM
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Agencies
[Federal Register Volume 75, Number 120 (Wednesday, June 23, 2010)]
[Proposed Rules]
[Pages 35721-35746]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-15251]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R6-ES-2010-0015]
[MO 92210-0-0008-B2]
RIN 1018-AV83
Endangered and Threatened Wildlife and Plants; Listing Ipomopsis
polyantha (Pagosa Skyrocket) as Endangered Throughout Its Range, and
Listing Penstemon debilis (Parachute Beardtongue) and Phacelia
submutica (DeBeque Phacelia) as Threatened Throughout Their Range
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), propose to
list Ipomopsis polyantha (Pagosa skyrocket), a plant species from
southwestern Colorado, as endangered throughout its range, and
Penstemon debilis (Parachute beardtongue) and Phacelia submutica
(DeBeque phacelia), two plant species from western Colorado, as
threatened throughout their ranges under the Endangered Species Act of
1973, as amended (Act). This proposal, if made final, would extend the
Act's protections to these species throughout their ranges. The Service
seeks data and comments from the public on this proposal.
DATES: We will consider comments received or postmarked on or before
August 23, 2010. We must receive requests for public hearings, in
writing, at the address shown in the FOR FURTHER INFORMATION CONTACT
section by August 9, 2010.
ADDRESSES: You may submit comments by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments on Docket No. FWS-R6-
ES-2010-0015.
U.S. mail or hand-delivery: Public Comments Processing,
Attn: [FWS-R6-ES-2010-0015]; Division of Policy and Directives
Management; U.S. Fish and Wildlife Service; 4401 N. Fairfax Drive,
Suite 222, Arlington, VA 22203.
We will post all comments on https://www.regulations.gov. This
generally means that we will post any personal information you provide
us (see the Public Comments section below for more information).
FOR FURTHER INFORMATION CONTACT: Patty Gelatt, Acting Western Colorado
Supervisor, U.S. Fish and Wildlife Service, Ecological Services Field
Office, 764 Horizon Drive, Building B, Grand Junction, CO 81506-3946;
telephone 970-243-2778, extension 26; fax 970-245-6933. If you use a
telecommunications device for the deaf (TDD), call the Federal
Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Public Comments
We intend that any final action resulting from this proposed rule
will be based on the best scientific and commercial data available and
be as accurate and as effective as possible. Therefore, we request
comments or information from the public, other government agencies, the
scientific community, industry, or any other interested party
concerning this proposed rule. We particularly seek comments
concerning:
(1) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to these species and regulations that may
be addressing those threats;
(2) Additional information concerning the range, distribution, and
population sizes of these species, including the locations of any
additional occurrences of these species;
(3) Any information on the biological or ecological requirements of
these species;
(4) Current or planned activities in the areas occupied by these
species and possible impacts of these activities on these species;
(5) Which areas would be appropriate as critical habitat for these
species and why they should be proposed for designation as critical
habitat; and
(6) The reasons why areas should or should not be designated as
critical habitat as provided by section 4 of the Act (16 U.S.C. 1531 et
seq.), including whether the benefits of designation would outweigh
threats to these species that designation could cause, such that the
designation of critical habitat is prudent.
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in the ADDRESSES section. We will not
consider comments sent by e-mail or fax or to an address not listed in
the ADDRESSES section.
We will post your entire comment--including your personal
identifying information--on https://www.regulations.gov. If you provide
personal identifying information in your hardcopy comments, you may
request at the top of your document that we withhold this information
from public review. However, we cannot guarantee that we will be able
to do so. We will
[[Page 35722]]
post all hardcopy comments on https://www.regulations.gov.
Comments and materials we receive, as well as supporting
documentation we used in preparing this proposed rule, will be
available for public inspection on https://www.regulations.gov, or by
appointment, during normal business hours, at the U.S. Fish and
Wildlife Service, Western Colorado Ecological Services Field Office
(see FOR FURTHER INFORMATION CONTACT section).
Final promulgation of the regulations concerning the listing of
these species will take into consideration all comments and additional
information that we receive, and may lead to a final regulation that
differs from this proposal.
Species Information and Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533) and implementing regulations
(50 CFR 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, 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.
Below is a species-by-species analysis of these five factors. The
species are considered in the following order: Ipomopsis polyantha,
Penstemon debilis, and Phacelia submutica.
Background--Ipomopsis polyantha
Previous Federal Actions
We first identified Ipomopsis polyantha as a taxon under review in
the 1983 Supplement to Review of Plant Taxa for Listing as Endangered
or Threatened Species (48 FR 53640, November 28, 1983). In that
document, we included the species as a Category 2 candidate, based on
our evaluation at that time. Category 2 candidate species were formerly
defined as ``taxa for which information now in the possession of the
Service indicates that proposing to list the taxa as Endangered or
Threatened species is possibly appropriate, but for which sufficient
data on biological vulnerability and threat(s) are not currently known
or on file to support proposed rules'' (48 FR 53641, November 28,
1983). We published our decision to discontinue candidate categories
and to restrict candidate status to those taxa for which we have
sufficient information to support issuance of a proposed rule on
December 5, 1996 (61 FR 64481), This resulted in the deletion of
Ipomopsis polyantha from the list of candidate taxa for listing. Since
1996, threats to the species have become more numerous and more
widespread. We added the species to the list of candidates again in the
2005Candidate Notice of Review (CNOR) (70 FR 24873, May 11, 2005) with
a listing priority number (LPN) of 2. Candidates are taxa for which we
have sufficient information on biological vulnerability and threats to
support preparation of a listing proposal, but for which development of
a listing regulation is precluded by other higher priority listing
activities. Candidate species are assigned an LPN (1-12, with 1 being
the highest priority) based on magnitude and immediacy of threats and
taxonomic status. A listing priority of 2 reflects threats that are
imminent and high in magnitude, as well as the taxonomic classification
of I. polyantha as a full species. We published a complete description
of our listing priority system in the Federal Register (48 FR 43098,
September 21, 1983).
Species Information
Ipomopsis polyantha is a rare plant endemic to shale outcrops in
and around Pagosa Springs in Archuleta County, Colorado. Suitable
habitat for the species is identified on about 191 acres (ac) (77
hectares (ha)) on the east edge of town, and on about 23 ac (9 ha)
approximately 10 miles (mi) (16 kilometers (km)) west of town.
Approximately 9 percent of the suitable habitat is on land managed by
the Bureau of Land Management (BLM) land, 12 percent on State and
County highway rights-of-way (ROWs), 78 percent on private lands, and
less than 1 percent on Pagosa Springs park land and county land
(Colorado Natural Areas Program (CNAP) 2007, pp. 1-5; Lyon 2005, pp. 1-
5; Lyon 2006a, pp. 1-2; Lyon 2006b, p. 1).
The Colorado Natural Heritage Program (CNHP) ranks Ipomopsis
polyantha as critically imperiled globally (G1) and in the State of
Colorado (S1) (CNHP 2006a, p. 1). The Nature Conservancy (TNC) and CNHP
also developed a scorecard that ranks I. polyantha among the most
threatened species in the State based on number of plants, quality of
the plants and habitat, threats, and adequacy of protection (CNHP and
TNC 2008, p. 102).
Ipomopsis polyantha is in the Polemoniaceae (phlox) family and was
originally described by Rydberg (1904, p. 634) as Gilia polyantha.
Grant (1956, p. 353) moved the species into the genus Ipomopsis. Two
varieties,G. polyantha var. brachysiphon and G. polyantha var.
whitingii, were recognized by Kearney and Peebles (1943, p. 59).
Currently available information indicates that I. polyantha is a
distinct species (Porter and Johnson 2000; Porter et al. 2003 in
Anderson 2004, p. 11). It is treated as such in the PLANTS database
(United States Department of Agriculture (USDA)/Natural Resource
Conservation Service (NRCS) 2003), and in the Integrated Taxonomic
Information System (2001).
Ipomopsis polyantha is an herbaceous biennial 12 to 24 inches (in.)
(30 to 60 centimeters (cm)) tall, branched from near the base above the
basal rosette of leaves. Deeply divided leaves with linear segments are
scattered up the stem. Stems and flower clusters are covered with
glandular hairs. Flower clusters are along the stem in the axils of the
leaves as well as at the top of the stem. The white flowers are 0.4 in.
(1 cm) long, with short corolla tubes 0.18 to 0.26 in. (0.45 to 0.65
cm) long, and flaring corolla lobes flecked with purple dots (Anderson
1988, p. 3). These dots are often so dense that they give the flower a
pinkish or purplish hue. The stamens extend noticeably beyond the
flower tube, and the pollen is blue (Grant 1956, p. 353), changing to
yellow as it matures (Collins 1995, p. 34). First-year plants form
basal rosettes of leaves. These rosettes produce flowering stalks
during the next growing season, or they may persist for more than 1
year without flowering, until they get enough moisture to flower Plants
produce abundant fruits and seeds, but have no known mechanism for long
distance dispersal (Collins 1995, pp. 111-112). After seeds are mature,
the plants dry up and die.
Pollination by bees is the most common means of reproduction for
Ipomopsis polyantha, and the primary pollinators are a honey bee (Apis
mellifera), metallic green bee (Augochlorella spp.), bumble bee (Bombus
spp.), and digger bee (Anthophora spp.) (Collins 1995, pp. 71-72).
Ipomopsis polyantha is limited to Pagosa-Winifred soils derived
from Mancos Shale. The soil pH is nearly neutral to slightly alkaline
(6.6 to 8.4). The elevation range is 6,800 to 7,300 feet (ft) (2,072 to
2,225 meters (m)). Plants occur in discontinuous colonies as a pioneer
species on open shale or as a climax species along the edge of
ponderosa pine/juniper/oak forested areas. In 1988, Anderson (p. 7)
reported
[[Page 35723]]
finding the highest densities under ponderosa pine forests with montane
grassland understory. Now the species is found mostly on sites that are
infrequently disturbed by grazing, such as road rights-of-way (ROWs)
that are fenced from grazing (as opposed to open range), lightly grazed
pastures, and undeveloped lots (Anderson 2004, p. 20).
Habitat for the species is characterized as suitable, potential, or
unsuitable. Suitable habitat has the attributes of soil and elevation
described above, and we further separate it into occupied habitat where
the plants have been observed and unoccupied habitat where soil and
elevation are suitable but no plants have been observed or no surveys
have been conducted. Potential habitat is identified remotely, using
aerial photographs, soil maps, and other available information, to
build a model of habitat that may support I. polyantha. The model has
not been ground-truthed in the field. Unsuitable habitat is found at
elevations and on soils that do not fit the profile for the species, or
habitat that has been altered by development, paving, or other human
activities so that the plants are prevented from growing there.
There are two known occurrences of Ipomopsis polyantha. Between its
description by C.F. Baker in 1899, and inventories in 1985, I.
polyantha was only known from along U.S. Route 84 (US 84) in the
vicinity of Pagosa Springs, Colorado (Anderson 1988, pp. 1-2, 15-16).
The Pagosa Springs occurrence is still the largest occurrence of the
species. In 1985, an additional occurrence was found about 10 mi (16
km) west of town along U.S. Route 160 (US 160) in a rural area called
Dyke (Anderson 1988, pp. 1-2). In 2002, another occurrence was
documented in a rural area called Mill Creek, about 1.2 mi (1.9 km)
east of Pagosa Springs (Anderson 2004, p. 13; CNHP 2008a, ID 228). The
Mill Creek area is now included in the Pagosa Springs occurrence, in
accordance with NatureServe criteria: occurrences are separated by at
least 0.62 mi (1 km) of unsuitable habitat or 1.24 mi (2 km) of
suitable habitat (NatureServe 2004, p. 1). The two known occurrences
are within about 13 mi (21 km) of each other, and collectively occupy
approximately about 50 ac (20 ha) of habitat within a range that
includes about 4 square mi (10.4 square km). Table 1 summarizes known
occupied habitat (50 ac (20 ha)) combined with suitable habitat not
verified as occupied within the two I. polyantha occurrences (total 234
ac (94 ha)).
Table 1. Occupied and Unsurveyed Suitable Habitat for Ipomopsis polyantha (CNAP 2007, pp. 1-5; Lyon 2005, p. 1;
Lyon 2006a, p. 1-2; Mayo 2008a, p. 1; CNHP 2008a, ID 228)
----------------------------------------------------------------------------------------------------------------
Flowering
Occurrence Land Ownership ac (ha) Plants Rosettes
----------------------------------------------------------------------------------------------------------------
Pagosa Springs including Mill Creek State ROW 19 (7.7) 3,029 3,083
----------------------------------------------------------------------------------------------------------------
County ROW 3 (1.2) 126 NA
----------------------------------------------------------------------------------------------------------------
Archuleta County 1 (0.4) 280 NA
Town of Pagosa Springs 1 (0.4) 3 15
Private (suitable) 184 (74) Unsurveyed NA
Private Corporation 3 (1.2) 156,126 173,189
----------------------------------------------------------------------------------------------------------------
Subtotals 211 (85) 159,564 176,287
----------------------------------------------------------------------------------------------------------------
Dyke State ROW 3 (1.2) 141 176
BLM 20 (8) 88 164
----------------------------------------------------------------------------------------------------------------
Subtotals 23 (9) 229 340
----------------------------------------------------------------------------------------------------------------
Totals All 234 (94) 159,793 176,627
----------------------------------------------------------------------------------------------------------------
The total occupied and surveyed habitat for Ipomopsis polyantha
covers about 50 ac (20 ha). Suitable habitat for the species has been
identified on about 211 acres (ac) (85 hectares (ha)) on the east side
of town, and on about 23 ac (9 ha) approximately 10 miles (mi) (16
kilometers (km)) west of town. Approximately 9 percent of the suitable
habitat is on federally owned Bureau of Land Management (BLM) land, 12
percent on State and County highway ROWs, 78 percent on private lands,
and less than 1 percent on Pagosa Springs Town park land and county
land (Colorado Natural Areas Program (CNAP) 2007). An estimated 184 ac
(74 ha), or 79 percent, of the suitable habitat exists on private
residential and agricultural land where plants have been observed from
a distance, but surveys have not been conducted. Without access to
these private lands, the extent of occupancy cannot be assessed.
The historical range of Ipomopsis polyantha is unknown, but likely
included a much broader area than the currently occupied habitat. Many
surveys of potential habitat in the Pagosa Springs area have been
conducted over the years with negative results. Potential habitat on
about 2,018 ac (817 ha) within the known range has not been surveyed
due to lack of access to private lands. All of this potential habitat
is close to or surrounded by suitable habitat, and is currently
proposed for development, including: Blue Sky Village 96 ac (39 ha);
Blue Sky Ranch 1,362 ac (551 ha); and Fairway 560 ac (227 ha) (see
Threat Factor A below).
None of the potential habitat identified to date extends beyond the
approximately 4-square-mi (10.4-square-km) occupied range of the
species. Reports of this species occurring in Arizona and New Mexico by
the PLANTS National Database and State floras actually pertain to the
two species that were formerly treated as varieties of Ipomopsis
polyantha (Anderson 2004, pp. 11, 15).
[[Page 35724]]
The Pagosa Springs occurrence of Ipomopsis polyantha is southeast
of the town along both sides of US 84. Occupied habitat extends
southward on the highway ROW for 3 mi (4.8 km) from the intersection
with US 160, and on private lands on both sides of the highway within
0.25 to 1.2 mi (0.4 to 1.9 km). In 1985, the estimated number of
flowering plants in this occurrence was 2,000 (Anderson 1988, p. 8).
During 2005-2006, 3,029 flowering plants and 3,083 rosettes were
counted on about 19 ac (7.7 ha) of highway ROW and immediately adjacent
private lands (CNAP 2007, pp. 1-5; Lyon 2005, p. 1; Lyon 2006a, pp. 1-
2). In 2005, an additional 156,126 plants and 173,189 rosettes were
found on a 3-ac (1.2-ha) private land site, which was a high density of
plants on a site where no plants had been observed in previous years
(Lyon 2005, pp. 3-4; Lyon 2007b, p. 1). The plants were found on a
hillside of Mancos Shale about 7 years after it was bladed, and are
still growing there because the ground has not been disturbed during
the growing season (Lyon 2007b, p. 2). I. polyantha quickly colonizes
unvegetated Mancos Shale near a seed source. The number of flowering
plants that appear in subsequent years depends on seed production and
the survival of rosettes that are not outcompeted by other species or
destroyed during ground disturbance.
In addition to the surveyed plants and rosettes, many flowering
Ipomopsis polyantha plants have been seen, but not counted, on private
residential/agricultural parcels along US 84 (Lyon 2006a, p. 1). An
estimated 184 ac (74 ha) of unsurveyed suitable habitat on private
lands exist within the Pagosa Springs occurrence.
The Dyke occurrence includes 0.5 mi (0.8 km) of highway ROW on both
sides of US 160, adjacent private land, and about half of a 40-ac (16-
ha) BLM parcel on the north side. On both of the ROWs and adjacent
pastures, more than 500 flowering plants were estimated in 1985
(Anderson 1988, p. 10). In 1991, about 250 plants were counted in
unused pasture on the south side, but no plants were found in
subsequent years after cattle were returned to the pasture (Collins
1995, pp. 111-112). The number of flowering plants and rosettes on the
US 160 ROW have fluctuated each year between 2005 and 2008. On the
north side ROW, the number of flowering plants and rosettes declined by
80 percent over the 4 years, to 9 and 8 respectively. On the south side
ROW, flowering plants increased 176 percent (to 141 plants), and
rosettes declined 9 percent (to 179 rosettes) (Mayo 2008a, p. 1). The
approximately 20-ac (8-ha) BLM parcel is the only federally managed
habitat for the species. There, in 2006, 88 flowering plants and 164
rosettes were found in clearings among ponderosa pine and shrubs (CNAP
2007, p. 2).
In addition to these extant occurrences, about 13 plants and 18
rosettes were found on a roadside in a residential area north of Pagosa
Springs in 2005. We do not consider this occurrence as extant, because
no plants have been found there since 2005. Surveys of roadsides and
private lands in this vicinity, and on additional potential habitat
north of town, have not detected any individuals of the species (Lyon
2005, p. 3).
In 2004, the total estimate of flowering plants throughout the
entire range of the species was 2,246 to 10,526 (Anderson 2004, p. 40).
Plant surveys from 2005 to 2007 document dramatic increases in the
number of flowering individuals and rosettes within the Pagosa Springs
occurrence at two sites on private land and on the US 84 ROW (CNAP
2007, pp. 1-2). Currently, the total estimate of flowering plants is
159,793 (see Table 1 above). This increase is primarily attributed to
the plants surveyed in 2005 and 2006 on the 3-ac (1.2-ha) private land
site in the Pagosa Springs occurrence. The rapid appearance of such a
dense patch of plants illustrates the specie's ability to colonize
barren Mancos Shale soil, and demonstrates the reproductive success of
the species; however, the sites where they grow are vulnerable to
habitat destruction. The trend in the species' status since 1988 is one
of fluctuating population size that is typical of biennial species,
combined with the loss of some plants due to development.
Summary of Factors Affecting Ipomopsis polyantha
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Ipomopsis polyantha is threatened with destruction of plants and
habitat due to commercial, residential, and agricultural property
development, and associated new utility installations and access roads.
We have documented recent losses of habitat and individuals at six
sites within the Pagosa Springs occurrence of the species, as described
in more detail below.
Within the Pagosa Springs occurrence, a residential and
agricultural development of about a dozen 35-ac (14-ha) parcels was
built prior to 2005 on occupied habitat east of US 84 (Archuleta County
Assessor 2008, p. 1). In 2005, when most residences were new, about 782
flowering plants were counted in meadows and along the fences and
access roads (Lyon 2005, pp. 1-2). By 2008, an increased number of
horses were pastured in the meadows, roadsides and driveways were
graded or widened, and few plants could be found as a result (Mayo
2008b, p. 1). This information indicates that Ipomopsis polyantha
plants are vulnerable to grazing and road improvements, and habitat can
be modified to exclude plants in as few as 3 years. In 2006, at another
location along US 84, a private landowner mowed several hundred feet of
occupied habitat on the highway ROW (Lyon 2006a, p. 1). No plants were
found at this site from 2006 to 2008, indicating that mowing destroys
plants and halts reproduction. In 2005, dense patches of flowering
plants were noted, from across the fence, in a privately owned meadow
along US 84. In 2007, a new home was built, and the meadow was mowed;
no plants could be seen at the same site in 2008 (Mayo 2008b, p. 2),
again indicating that mowing destroys plants and inhibits reproduction.
During 2005 and 2006, a sewer line installation on the US 84 ROW
resulted in the loss of about 498 plants and 541 rosettes, and
modification of about 1,473 ft (449 m) of roadside habitat (Mayo 2008c,
p. 8). The Colorado Department of Transportation (CDOT) and Archuleta
County consulted with us, and agreed on avoidance measures for this
project, but contractors failed to follow the protocol (Mayo 2008c, pp.
1-4). In 2008, only a few flowering plants and rosettes were found at
this site; all of the plants were in one spot near plants on an
adjacent property not disturbed by the sewer line project (Mayo 2008c,
p. 8). This incident demonstrates that I. polyantha cannot quickly
recover from soil disturbance.
Utility installations and construction activities can eliminate
habitat and destroy Ipomopsis polyantha. As a result of careful
planning, in 2007, power line maintenance was completed within occupied
habitat in the Pagosa Springs occurrence with negligible damage to
adult plants. Rosettes in the path of maintenance actions were
transplanted to suitable habitat in the town park. The 278 transplants
survived the winter and produced about 27 flowering plants. However, no
surviving rosettes could be relocated in the fall (Coe 2007, pp. 2-3).
A second attempt at transplanting rosettes to save them from
destruction during utility installations also has not been effective
[[Page 35725]]
in producing new rosettes in the third year (Brinton 2007, pers.
comm.). Unless effective methods are developed, most plants that cannot
be avoided during utility installations and construction activities are
unlikely to survive and reproduce. Whether the species can survive
translocation under other circumstances remains uncertain.
Primary land use within the range of Ipomopsis polyantha has
historically been agricultural, with homes and horses or cattle on
parcels of 35 ac (14 ha) or more. Several small businesses now occur
along US 84 within the Pagosa Springs occurrence. The intersection of
US 160 and US 84 is zoned by the Town of Pagosa Springs for businesses,
and commercially zoned land is currently available for development. The
County is also considering sites in this area for new municipal
buildings; one of the sites under consideration contains the highest
density of I. polyantha occurrence. These current and potential
conversions of agricultural lands to residential and commercial
development are incompatible with conservation of I. polyantha in the
long term because they cause direct mortality and permanent loss of
habitat, whereas habitat modified by grazing may be recovered by
changes in management.
The privately owned property across the entire range of Ipomopsis
polyantha was scheduled for development in the Archuleta County and
Town of Pagosa Springs Community Plan (2000). In this plan, all areas
occupied by I. polyantha on private land outside of the Town limits are
planned for low (35 ac (14 ha)), medium (3 to 35 ac (1.2 to 14 ha)), or
high (2 to 5 ac (0.81 to 2 ha)) density housing. Residential
development is increasing rapidly in the County. The population of
Archuleta County was 5,000 in 1990; the projection is 15,000 people by
2010 and 20,000 by 2020 (Archuleta County and Town of Pagosa Springs
2000, pp. 5-7). Based on the rate of current and proposed development
over the entire range of the species, 85 percent of occupied and
suitable habitat and all potential habitat could be modified or
destroyed within 5 to 10 years, putting the species at risk of
extinction.
The County plan for agricultural and large-lot residential
development along US 84 became obsolete in 2008, with the Pagosa Town
Council's preliminary approval of a 96-ac (39-ha) Blue Sky Village
annexation (Aragon 2008a, pp. 1-2). The proposed development plan is
for a mixed commercial and high-to-low density residential village
(Hudson 2008, p. 1). The 96-ac (39-ha) parcel is adjacent to the
highest density of Ipomopsis polyantha plants, and includes about 2,562
ft (781 m) of potential habitat on US 84 frontage at the center of the
species' distribution (Archuleta County Assessor 2008, p. 1). Occupied
habitat also borders the southern edge of the property. Reducing
habitat available to the Pagosa Springs occurrence of I. polyantha will
limit its ability to disperse and repopulate after impacts.
In addition to the loss of potential habitat on private land for
the plants, the proposed annexation will require access roads, utility
installations, and acceleration and deceleration lanes along the
highway ROW. Plants and habitat will likely be destroyed by this
infrastructure construction. The Blue Sky Village development will
significantly reduce the amount of potential habitat within the
species' range. Location of the development between the highest density
of plants and the rest of the Pagosa Springs occurrence on the east
side of US 84 will further fragment the habitat that has already been
impacted by commercial, residential, and agricultural land uses.
The Blue Sky Ranch development of 1,362 ac (551 ha), plus 2,819 ft
(859 m) of US 84 frontage, is another annexation being considered
within potential Ipomopsis polyantha habitat. This project would
include single and multi-family residential housing, a hotel and
conference center, a golf course with clubhouse, and an equestrian
center with riding trails and a multi-use arena (Aragon 2008b, p. 2).
A development of 560 ac (227 ha), including about 1 mi (1.6 km) of
frontage along the west side of US 84, also is being considered for
annexation within potential habitat that has not been surveyed for
plants (Aragon 2008a, p. 2; Archuleta County Assessor 2008, p. 1).
The above three development proposals within the Pagosa Springs
occurrence cover a total of 2,018 ac (817 ha) of potential habitat for
the plants that have not been surveyed due to restricted access. The
proposed developments include frontage along the US highway 84 ROW that
currently provides 34 percent of the total habitat occupied by the
plants (Archuleta County 2008, p. 1). Plants and habitat on this ROW
are likely to be disturbed or removed by construction of new access
roads, acceleration lanes, and utilities to accommodate the
development.
The Archuleta County and Town of Pagosa Springs revised 2004 Trails
Plan (2004, p. 18) calls for an 8-ft (2.4 m) wide, 2.5-mi (4 km) long,
paved bike path on the highway ROW from US 160 south along US 84 in
occupied Ipomopsis polyantha habitat. This route, prioritized for
completion as soon as funding is available, would eliminate about 50
percent of the occupied habitat on the highway ROW and 80 percent of
the total occupied area in the Pagosa Springs occurrence (see Table 1
above). Another planned paved bike trail, parallel to US 160 and
through the Dyke occurrence of I. polyantha, is on the low priority
list in the Trails Plan (Archuleta County and Town of Pagosa Springs
2004, p. 28). Development of this bike trail would eliminate the
portion of the Dyke occurrence located on the south side of the highway
where the trail would be located.
Distribution of Ipomopsis polyantha on highway ROWs makes this
species susceptible to threats associated with highway activities and
maintenance. Exotic grasses planted by CDOT along roadsides dominate
the ROW between pavement and ditch, limiting most I. polyantha plants
to the ROW bank between ditch and fence. This limitation to the
species' habitat along roadsides is significant because so little
habitat exists elsewhere for the species. I. polyantha plants growing
among thistles were killed by herbicide within the highway ROW along US
84 in 2004, when the thistles were treated with herbicide (Anderson
2004, p. 36). Since that time, Archuleta County has discontinued
broadcast herbicide use and mowing on ROWs within the species' range.
However, the planted exotic grasses continue to limit the species'
habitat.
Highway ROWs provide about 50 percent of the occupied habitat for
Ipomopsis polyantha. All highway ROW habitat is at risk of disturbance
by construction of new access roads or acceleration lanes, bike paths,
and utilities installation or maintenance. Such construction results in
direct loss of I. polyantha individuals or reduced suitability of its
habitat by altering the soil characteristics or displacing the seed
bank (Anderson 2004, p. 36).
We determined that the present and threatened destruction,
modification, and fragmentation of Ipomopsis polyantha habitat from
ongoing commercial and residential development, associated new utility
installations, construction of new access roads and bike paths,
competition from introduced roadside grasses and other impacts
associated with proximity to highways are significant and imminent
threats to the species throughout its range. At this time, the species
primarily persists on highway ROWs and private lands scheduled for
development. Development planned for
[[Page 35726]]
the next 5 to 10 years will likely: (1) Impact over 2,000 ac (809 ha)
of potential habitat; (2) potentially eliminate 167 of the 214 ac (68
of 87 ha) of existing occupied and suitable habitat on private lands;
and (3) potentially eliminate about 34 percent of the highway ROW
(occupied) habitat. Combined, these impacts would relegate the species
primarily to small, fragmented portions of highway ROWs and a few,
small, lightly-used private pastures putting the species in danger of
extinction.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Activities resulting in overutilization of Ipomopsis polyantha
plants for commercial, recreational, scientific, or educational
purposes are not known to exist. Therefore, this factor is not
addressed in this proposal.
C. Disease or Predation
Disease
Disease is not known to affect Ipomopsis polyantha. Therefore,
disease is not addressed in this proposal.
Predation
This species is threatened by destruction of flowering plants,
rosettes, and seeds due to concentrated livestock disturbance and some
herbivory. Observations of the ``fence line effect''--healthy plants
outside the fence and impacted plants inside the fence--at several
locations on private land used for cattle and horse grazing indicate
that Ipomopsis polyantha does not tolerate intensive livestock grazing
(Anderson 2004, p. 30). For example, grazing by horses at a
residential/agricultural development within the Pagosa Springs
occurrence in 2005 resulted in few I. polyantha plants 3 years later
(Mayo 2008b, p. 1). Over-the-fence observations from seven locations
(pastures) in 2009 found few or no plants in the three heavily grazed
pastures and numerous plants in the adjacent pastures with light or no
grazing (Glenne 2010, pp. 1-3). We have no data to indicate whether the
plant destruction results from herbivory or from trampling. I.
polyantha is not found in heavily grazed pastures, but occurrences have
been observed in lightly grazed horse pastures and abandoned pastures
(CNAP 2007, p. 6). Plants could possibly recolonize a pasture if
livestock numbers were reduced sufficiently and the seed bank was still
viable, or if there was a seed source nearby, such as on the ungrazed
side of a fence. Indications are that the species may be compatible
with light grazing, but the level of impact and the threshold of
species' tolerance have not been studied. Evidence indicates that few
plants persist in areas of continual grazing (Collins 1995, pp. 107,
111, 112). We determined that destruction of flowering plants,
rosettes, and seeds due to heavy livestock use is a significant and
imminent threat to I. polyantha.
D. The Inadequacy of Existing Regulatory Mechanisms
Local Laws and Regulations
City and county ordinances have the potential to affect Ipomopsis
polyantha and its habitats. Zoning that protects open space can retain
suitable habitat, and zoning that allows commercial development can
destroy or fragment habitat. We know of no city or county ordinances
that provide for protection or conservation of I. polyantha or its
habitat. Archuleta County road maintenance crews refrain from mowing or
broadcast spraying ROWs within the range of Ipomopsis polyantha
voluntarily, that is, without the mandate or support of regulations.
However, there is no law, regulation, or policy requiring them to do
so.
New annexation of 2,018 ac (817 ha) into the Town of Pagosa Springs
will change land use from 35-ac (14-ha) agricultural parcels to
commercial and small lot residential, with anticipated adverse impacts
to the Pagosa Springs occurrence of I. polyantha. This land use
conversion, as described in Factor A above, is the most significant
threat to the species, because development planned for the next 5 to 10
years will likely impact all known potential habitat and 17 of 25 ROW
acres (6.9 of 10 ha), and relegate the species to private residential
areas and small, fragmented portions of highway ROWs.
State Laws and Regulations
No State regulations protect rare plant species in Colorado.
Ipomopsis polyantha is classified by CNHP as a G1 and S1 species, which
means it is critically imperiled across its entire range and within the
State of Colorado (CNHP 2006a, p. 1). The CDOT has drafted best
management practices for ROWs within I. polyantha habitat in
collaboration with the Service (Peterson 2008, p. 1). In 2006,
voluntary measures to minimize impacts to plants from a sewer line
installation along US 84 were recommended by CDOT, but not implemented
by the contractors (Mayo 2008c, pp. 1-4).
Federal Laws and Regulations
Ipomopsis polyantha is on the sensitive species lists for the U.S.
Forest Service (USFS) and the BLM (USFS 2009, p. 6; BLM 2008b, p. 47).
Occupied habitat has not been found on USFS land. In 2006, we learned
that the Dyke occurrence extends onto 20 ac (8 ha) of BLM land (Lyon
2007b, pp. 3, 12, 13); 88 plants and 164 rosettes were found there in
2007 (CNAP 2007, p. 2). This BLM parcel was withdrawn from a proposed
land exchange so that the plant habitat would remain under Federal
management (Brinton 2009, pers. comm.; Lyon 2007b, p. 3). The species
has no Federal regulatory protection for approximately 91 percent of
the total known occupied and suitable habitat. It occurs mostly on
State and private land (see Table 1 above), and development of these
areas will likely require no Federal permit or other authorization.
Therefore, projects that affect it are usually not analyzed under the
National Environmental Policy Act (NEPA)(42 U.S.C. 4321 et seq.).
We determined that the inadequacy of existing regulatory mechanisms
is a significant and imminent threat to Ipomopsis polyantha, because 91
percent of the known range of the species is on State and private lands
that carry no protective regulations to ameliorate activities that will
impact the species.
E. Other Natural or Manmade Factors Affecting Its Continued Existence
The adaptation of Ipomopsis polyantha to Pagosa-Winifred soils
derived from Mancos Shale limits it to about 4 square mi (10.4 square
km) within a 13-mi (21-km) range of fragmented habitat on outcrops of
Mancos Shale. The species has specific physiological requirements for
germination and growth that may prevent its spread to other locations
(Anderson 2004, pp. 23-24). In greenhouse trials, seeds will germinate
and grow on other soils, but they grow much faster on Mancos Shale
soils (Collins 1995, p. 114). Faster growth may give I. polyantha a
competitive advantage on relatively barren Mancos shale that it lacks
on other soils where its smaller seedlings have more competition from
other plants for nutrients and water. The species produces more seed
when it is cross-pollinated (Anderson 2004, p. 23); therefore, existing
and foreseeable fragmentation of habitat may cause gene flow to be
obstructed. Pollinator-mediated pollen dispersal is typically limited
to the foraging distances of pollinators, and no bee species is
expected to travel more than 1 mi (1.6 km) to forage (Tepedino 2009, p.
11). Thus, it is likely that the occurrence of
[[Page 35727]]
about 191 plants west of Pagosa Springs is genetically isolated from
the other occurrence several miles (kilometers) away. Spatially
isolated plant populations are at higher risk of extinction due to
inbreeding depression, loss of genetic heterogeneity, and reduced
dispersal rates (Silvertown and Charlesworth 2001, p. 185).
Ipomopsis polyantha shows great differences in plant numbers from
year to year, probably because the plants are biennial and grow from
seed. This trait makes them more vulnerable than perennials to changes
in environment, including timing and amount of moisture, and length of
time since disturbance. With increased time after disturbance,
competition from other plants, both native and nonnative, increases
(CNAP 2008a, p. 4). As a biennial species, I. polyantha also may be
vulnerable to prolonged drought. During drought years, seeds may not
germinate and plants may remain as rosettes without flowering or
producing a new crop of seeds.
Climate change could potentially impact Ipomopsis polyantha.
Localized projections indicate the southwest may experience the
greatest temperature increase of any area in the lower 48 States (IPCC
2007, p. 30). A 10- to 30-percent decrease in precipitation in mid-
latitude western North America is projected by the year 2050, based on
an ensemble of 12 climate models (Milly et al. 2005, p. 1). Climate
modeling at this time has not been refined to the level that we can
predict the amount of temperature and precipitation change within the
limited range of I. polyantha. Therefore, this analysis is speculative
based on what the data indicate at this time. When plant populations
are impacted by reduced reproduction during drought years, they may
require several years to recover. Climate change may exacerbate the
frequency and intensity of droughts in this area and result in reduced
species' viability as the dry years become more common. As described
above, I. polyantha is sensitive to the timing and amount of moisture
due to its biennial life history. Thus, if climate change results in
local drying, the species could experience a reduction in its
reproductive output.
Recent analyses of long-term data sets show accelerating rates of
climate change over the past two or three decades, indicating that the
extension of species' geographic range boundaries towards the poles or
to higher elevations by progressive establishment of new local
occurences will become increasingly apparent in the short term (Hughes
2000, p. 60). The limited geographic range of the Mancos Shale
substrate that underlies the entire Ipomopsis polyantha habitat likely
limits the ability of the species to adapt by shifting occurrences in
response to climatic conditions.
We determined that the natural and human-caused factors of specific
soil and germination requirements, fragmented habitat, effects of
drought and climate change, and lack of proven methods for propagation
present an imminent and moderate degree of threat to Ipomopsis
polyantha across the entire range of the species.
Background--Penstemon debilis
Previous Federal Actions
We first included Penstemon debilis as a category 2 candidate
species in the February 21, 1990, Review of Plant Taxa for Listing as
Endangered or Threatened Species (55 FR 6184). Category 2 candidate
species were defined as ``[t]axa for which there is some evidence of
vulnerability, but for which there are not enough data to support
listing proposals at this time'' (55 FR 6185, February 21, 1990). In
1996, we abandoned the use of numerical category designations and
changed the status of P. debilis to a candidate under the current
definition. We published four CNOR lists between 1996 and 2004, and P.
debilis remained a candidate species with a LPN of 5 on each (62 FR
49398, September 19, 1997; 64 FR 57534, October 25, 1999; 66 FR 54808,
October 30, 2001; 67 FR 40657, June 13, 2002). A LPN of 5 is assigned
to species with non-imminent threats of a high magnitude.
On March 15, 2004, the Center for Native Ecosystems (CNE) and the
Colorado Native Plant Society petitioned us to list Penstemon debilis
(CNE 2004a, p. 1). We considered the information provided in their
petition when we prepared the 2004 CNOR. In the 2004 CNOR, P. debilis
remained a candidate species with a listing priority of 5 (69 FR 24876,
May 4, 2004).
On May 11, 2004, we received a petition from the Center for
Biological Diversity (CBD) to list 225 species we previously had
identified as candidates for listing, including Penstemon debilis (CBD
2004, p. 6). Under requirements in section 4(b)(3)(B) of the Act, the
CNOR and Notice of Findings on Resubmitted Petitions published on May
11, 2005 (70 FR 24870), raised the LPN of P. debilis from 5 to 2 but
also included a finding that the immediate issuance of a proposed
listing rule and the timely promulgation of a final rule for each of
225 petitioned species, including P. debilis, was warranted but
precluded by higher priority listing actions, and that expeditious
progress was being made to add qualified species to the Lists (70 FR
24870, May 11, 2005).
On November 15, 2004, the CNE issued a 60-day notice of intent to
sue for violation of section (4)(b)(3)(A) of the Act with respect to
the petition to list Penstemon debilis (CNE 2004b, pp. 1-2). On January
25, 2005, Biodiversity Conservation Alliance and seven other entities
filed an amended complaint regarding our failure to list P. debilis and
five other species. As part of a settlement agreement, plaintiffs
withdrew their lawsuit regarding P. debilis.
In the 2005 CNOR (70 FR 24870), as stated above, the listing
priority number for Penstemon debilis was changed from 5 to 2 based on
an increase in the intensity of energy exploration along the Roan
Plateau escarpment, making the threats to the species imminent (70 FR
24870, May 11, 2005). A listing priority of 2 represents threats that
are both imminent and high in magnitude. CNOR lists published in 2006
and 2007 maintained P. debilis as a candidate species with a listing
priority of 2 (71 FR 53756, September 12, 2006; 72 FR 69034, December
6, 2007).
In each assessment since its recognition as a candidate species in
1996, we determined that publication of a proposed rule to list the
species was precluded by our work on higher priority listing actions.
However, in 2008, we received funding to initiate the proposal to list
Penstemon debilis.
Species Information
Penstemon debilis is a rare plant, endemic to oil shale outcrops on
the Roan Plateau escarpment in Garfield County, Colorado. This species
is known by the common names Parachute beardtongue and Parachute
penstemon. P. debilis is classified by the CNHP as a G1 and S1 species,
which means it is critically imperiled across its entire range and
within the State of Colorado (CNHP 2008b, p. 14). The total estimated
number of known plants is approximately 4,000 individuals (CNHP 2006b,
p. 1; CNHP 2009a, p. 1; CNHP 2009b, p. 1; CNHP 2009c, p. 1; CNHP 2009d,
p. 2). Approximately 82 percent of the known plants are on private land
owned by a natural gas and oil shale production company. Most of the
remaining 18 percent occur in one occurrence on BLM land that was
recently leased under a new Resource Management Plan (RMP) amendment
(BLM 2008a, Record of Decision (ROD) p. 2). In recent years, energy
development has increased in this area on both private and Federal
lands.
[[Page 35728]]
Traditionally Penstemon has been included in the Scrophulariaceae
(figwort family). Phylogenetic studies based on DNA sequences of taxa
in this and related plant families over the last 10 years have
necessitated realignment of several genera in these groups. Apart from
a nomenclatural discrepancy, Penstemon has been shown to be a part of
the Plantaginaceae (plantain) family, since 2001. The chronology and
summary of the placement of Penstemon in the Plantaginaceae is
presented by Oxelman et al. (2005, p. 415). We recognize this placement
and will make the appropriate attribution in the proposed amendments to
50 CFR 17.12(h) at the end of this document. The text will include the
family name as Plantaginaceae.
Penstemon debilis was discovered in 1986, and was first described
by O'Kane and Anderson in 1987 (pp. 412-416. No challenges have been
made to the taxonomy as first put forward by the authors. Penstemon
debilis is a mat-forming perennial herb with thick, succulent, bluish
leaves, each about 0.8 in. (2 cm) long and 0.4 in. (1 cm) wide. Plants
produce shoots that run along underground, forming what appear as new
plants at short distances away. Individual P. debilis plants are able
to survive on the steep, unstable, shale slopes by responding with stem
elongation as leaves are buried by the shifting talus. Buried stems
progressively elongate down slope from the initial point of rooting to
a surface sufficiently stable to allow the development of a tuft of
leaves and flowers (O'Kane and Anderson 1987, pp. 414-415). Flowers are
funnel-shaped, are white to pale lavender, and flower during June and
July. P. debilis plants produce a low number of seeds, are primarily
outcrossers, and have many different pollinators that vary between
occurrences (McMullen 1998, p. 26). None of the pollinators are
specialists to P. debilis, nor are any of them rare (McMullen 1998, p.
31). We know little about the lifecycle of Penstemon debilis with
regard to generational timetables.
Penstemon debilis seems to be at least somewhat adapted to
disturbance. Each of the known occurrences of the species contains high
levels of physical disturbance (McMullen 1998, p. 81). Many of the
characteristics that are most similar among sites promote continual
disturbance: steep slopes, unstable shale channer surface layers, and
no surface soil (McMullen 1998, p. 82). In fact, two of the largest P.
debilis occurrences, are on recent mine talus slopes where
anthropogenic disturbance was very high as recently as 1994 (McMullen
1998, p. 82). One occurrence was recorded to have several hundred
individuals in 1994, but no individuals can be found at this site today
(McMullen 1998, p. 82). This may be a result of a reduction in the
disturbance levels through successional processes such as soil
development and increased vegetative cover (McMullen 1998, p. 82).
Penstemon debilis may be considered a pioneer species that disperses to
recent disturbances, flourishes, and goes locally extinct if soil
conditions become stable (McMullen 1998, p. 82).
Penstemon debilis grows on steep, oil shale outcrop slopes of white
shale talus at 8,000 to 9,000 ft (2,400 to 2,700 m) in elevation on the
southern escarpment of the Roan Plateau above the Colorado River west
of the town of Parachute, Colorado. The Roan Plateau falls into the
geologic structural basin known as the Piceance Basin. Average annual
precipitation at Parachute, Colorado, is 12.75 in. (32.4 cm) (IDcide
2009, p. 1). P. debilis is found only on the Parachute Creek Member of
the Green River Formation. P. debilis is often found growing with other
species endemic to the Green River formation, including Astragalus
lutosus (dragon milkvetch), Festuca dasyclada (Utah fescue), Mentzelia
argillosa (Arapien stickleaf), and Thalictrum heliophilum (sun-loving
meadowrue), as well as several non-endemics (O'Kane & Anderson 1987, p.
415).
The historical range and distribution for this species is unknown.
All of the currently known occurrences occur on about 56 ac (23 ha) in
Garfield County. The Green River geologic formation to which the plant
is restricted is the major source of oil shale in the United States.
Although this formation is underground throughout most of the Piceance
Basin, it is exposed on much of the southern face of the Roan Plateau.
The total area of the plant's geographic range is about 2 mi (3 km)
wide and 8 mi (13 km) long. Prior to 1997, two occurrences of P.
debilis were known. In 1997, the CNHP used existing habitat and
distribution information, along with soils, geology, and aerial
photographs, to select target survey areas. The ensuing survey resulted
in the discovery of two new occurrences (Spackman et al. 1997, p. 6).
Two other occurrences were first recorded by BLM in 1997 and 2005 at
oil shale mine sites (CNHP 2009a, p. 1; CNHP 2009d, p. 1). Another
occurrence of approximately 12 plants was reported in June 2009 (Graham
2009a, pp. 1-2). It is likely that unknown occurrences exist, because
many areas are simply inaccessible to surveyors due to steep terrain or
private land ownership or both.
Penstemon debilis occurs at seven known occurrences, four of which
are rated by CNHP as having ``good to excellent'' estimated viability
based on population size, individual plant sizes, and site ecology
(CNHP 2006b, p. 1; CNHP 2009a, p. 1; CNHP 2009b, p. 1; CNHP 2009c, p.
1; CNHP 2009d, p. 2) (see Table 2 below). The largest occurrence (Mount
Callahan Natural Area) of 2,100 to 2,240 plants grows on lands owned by
an energy development company (CNAP 2006, p. 1). The Mount Callahan
Ridge occurrence, with an estimated 650 plants, grows on lands owned by
the same energy development company (CNAP 2006, pp. 1-2). The Anvil
Points Road occurrence grows on lands administered by the BLM and has
an estimated 700 plants (CNHP 2009d, p. 2). The Mount Logan Mine
occurrence grows on lands owned by both the energy development company
(approximately 90 percent) and BLM (10 percent), and has 533 plants
(CNHP 2009a, p. 1).
Two additional Penstemon debilis occurrences on BLM land are
considered to have ``poor'' estimated viability (CNHP 2009e, p. 1; CNHP
2009f, p. 1). The Anvil Points occurrence had 200 to 300 plants
reported in 1994, but only three plants could be found in 1998 (CNHP
2009e, p. 1). The latest survey in 2006 found no plants at this
occurrence (CNHP 2009e, p. 1). It appears that the decline of this
occurrence was a result of natural processes including competition by
surrounding vegetation (DeYoung 2008a, p. 1). The area including this
habitat also was leased under the BLM August 2008 lease sale (BLM
2008b, p. 3; Ewing 2008a, p. 7).
The Mount Logan Road occurrence, discovered in 1996 on a road cut,
had 10 plants, of which only 3 were found in 2005 (CNHP 2009f, p. 1).
Because these two occurrences have so few individuals, they are
considered to have poor viability by CNHP, and we consider them not
viable into the future.
The Smith Gulch occurrence of approximately 12 plants was reported
in June 2009 (Graham 2009a, pp. 1-2). This occurrence has not been
rated by CNHP; however, it is small (12 plants) and, because of its
positioning in a drainage, has a high potential for being destroyed by
a rain event (Graham 2009a, pp. 1-2).
[[Page 35729]]
Table 2. Current and Historically Known Penstemon debilis Occurrences
----------------------------------------------------------------------------------------------------------------
of
Occurrence Viability Plants ac (ha) Land Ownership
----------------------------------------------------------------------------------------------------------------
Mt. Callahan Natural Area Excellent 2,100-2,240 32 (12.9) Private
----------------------------------------------------------------------------------------------------------------
Anvil Points Road Good 700 5 (2) BLM
----------------------------------------------------------------------------------------------------------------
Mount Logan Mine Good 533(50 on BLM) 2 (0.8) Private and BLM
----------------------------------------------------------------------------------------------------------------
Mount Callahan Ridge Good 650 4 (1.6) Private
----------------------------------------------------------------------------------------------------------------
Mount Logan Road Poor 3 7 (2.8) BLM
----------------------------------------------------------------------------------------------------------------
Anvil Points Poor 0 6 (2.4) BLM
----------------------------------------------------------------------------------------------------------------
Smith Gulch Unrated 12 not reported BLM
----------------------------------------------------------------------------------------------------------------
Total 3,998 - 4,138 56 (22.7) ..................
----------------------------------------------------------------------------------------------------------------
The total estimated number of Penstemon debilis in the wild is
currently 3,998 to 4,138 individuals. The occurrences on BLM land
represent about 18 percent of the total plants counted and estimated.
An energy development company owns land that contains approximately 82
percent of the total plants. We have no information to indicate an
overall species trend.
Summary of Factors Affecting Penstemon debilis
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Penstemon debilis habitat is threatened by energy development and
associated impacts. Of the four known viable occurrences (Mount
Callahan Natural Area, Anvil Points Road, Mount Logan Mine, Mount
Callahan Ridge), all but the Anvil Points Road occurrence are on lands
wholly or partially owned by an energy development company. All four
viable occurrences, which exist on the Roan Plateau, face ongoing or
potential threats, including: oil and gas development, oil shale
extraction and mine reclamation, and road maintenance and vehicle
access through occurrences.
The Piceance Basin, including federal and private lands surrounding
the Roan Plateau, has experienced a boom in natural gas production in
recent years. The BLM projects that around 3,916 billion cubic feet of
natural gas will be developed over the next 20 years from the portion
of the Roan Plateau that was addressed in the new RMP amendment (CNE
2004a, p. 44). Oil and gas exploration and development continues to
increase each year on and around the Roan Plateau. In 2003, 566 new
wells were permitted in Garfield County: 796 in 2004; 1,508 in 2005
(Colorado Oil and Gas Conservation Commission (COGCC 2006, p. 1); 1,844
in 2006; 2,550 in 2007 (COGCC 2008, p. 1); and 2,888 in 2008 (COGCC
2009a, p. 1). Because of a decrease in natural gas prices, new well
permits decreased in 2009 to 743 (Webb 2009, p. 1), as of June 3, 2009
(COGCC 2009a, p. 1). This number is down from the 1,029 wells permitted
by the same time in 2008, but is still higher than the 566 wells
permitted in Garfield county in all of 2003 (COGCC 2008, p. 1).
Energy exploration and development includes construction of new
unpaved roads, well pads, disposal pits, evaporation ponds, and
pipeline corridors, as well as cross country travel by employees. Each
of these actions has the potential to cause direct impacts such as
plant removal and trampling, and indirect impacts to Penstemon debilis
such as dust deposition and loss of habitat for pollinators. The
ramifications of direct impacts are easily assessed if witnessed. Plant
removal, contact with herbicide or ice-melting chemicals, and trampling
can cause death of plants. Because P. debilis was unknown as a species
until 1987, and most of the occurrences are on private land or in
remote locations on public land, the impacts may go unnoticed. For
example, impacts to the Mount Logan Mine occurrence were unknown until
the occurrence was discovered in 2005; even after discovery, further
mine-related impacts occurred because the remote location of the mine
made it difficult for BLM to manage the occurrence (CNHP 2009b, p. 1;
Ewing 2009a, p. 4).
Indirect effects to Penstemon debilis from energy exploration are
less easily assessed. Road traffic on unpaved roads increases dust
emissions in previously stable surfaces (Reynolds et al. 2001, p.
7126). For every vehicle traveling one mile (1.6 km) of unpaved roadway
once a day, every day for a year, approximately 2.5 tons of dust are
deposited along a 1,000-foot (305-m) corridor centered on the road
(Sanders 2008, p. 20). Vascular plants can be greatly affected within
the zone of maximum dust fall (i.e., the first 1000 ft (305 m) from the
road) (Everett 1980, p. 128). Excessive dust may affect photosynthesis,
affect gas and water exchange, clog plant pores, and increase leaf
temperature leading to decreased plant vigor and growth (Ferguson et
al. 1999, p. 2; Sharifi et al. 1997, p. 842). All of the viable
occurrences of P. debilis are within 300 ft (91 m) of roads. Further
energy development would likely increase road density and traffic
volume.
Other indirect impacts can occur due to a loss of pollinator
habitat. Penstemon debilis requires an insect pollinator to reproduce
(McMullen 1998, p. iii). McMullen (1998) concluded that pollinators for
P. debilis were generalists and were not limiting at that time (prior
to the energy boom). However, Tepedino (2009) described how the
pollination biology of another Piceance Basin rare plant (Physaria
obcordata) is being impacted by energy development. He described that
any energy development that reduces the general level of available
floral vegetation has a detrimental effect on pollinators' ability to
reproduce, subsequently resulting in fewer pollinators and reduced
ability of the dependent plant to reproduce (Tepedino 2009, pp. 16-17).
A large parcel of land including habitat occupied by the Anvil
Points Road occurrence was offered and sold for oil and gas leasing
under the BLM August 2008 lease sale (DeYoung 2008b, p. 1; BLM 2008b,
p. 1; Ewing 2008a, p. 7). This lease is currently being contested in
court. Increased energy exploration in the Anvil Points Road area may
increase maintenance and vehicle access on the unstable road that
[[Page 35730]]
transects the Penstemon debilis occurrence and increase the likelihood
of effects to P. debilis due to construction of additional roads and
other facilities associated with oil and gas exploration.
Oil shale mining has impacted Penstemon debilis occurrences. Oil
shale extraction activities occurred on the Roan Plateau in the early
1980s and into the 1990s (COBiz 2008, pp. 3-4). This extraction
impacted the Mount Logan Mine and Anvil Points Road occurrences.
Because P. debili