Endangered and Threatened Wildlife and Plants; Endangered Species Status for Trichomanes punctatum ssp. floridanum, 60439-60465 [2015-25299]
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Vol. 80
Tuesday,
No. 193
October 6, 2015
Part II
Department of the Interior
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Fish and Wildlife Service
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Endangered Species
Status for Trichomanes punctatum ssp. floridanum (Florida Bristle Fern);
Final Rule
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Federal Register / Vol. 80, No. 193 / Tuesday, October 6, 2015 / Rules and Regulations
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R4–ES–2014–0044;
4500030113]
RIN 1018–AY97
Endangered and Threatened Wildlife
and Plants; Endangered Species
Status for Trichomanes punctatum
ssp. floridanum (Florida Bristle Fern)
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), determine
endangered species status under the
Endangered Species Act of 1973 (Act),
as amended, for Trichomanes
punctatum ssp. floridanum (Florida
bristle fern), a plant subspecies from
Miami-Dade and Sumter Counties,
Florida. The effect of this regulation will
be to add this subspecies to the Federal
List of Endangered and Threatened
Plants and extend the Act’s protections
to this subspecies.
DATES: This rule becomes effective on
November 5, 2015.
ADDRESSES: This final rule is available
on the internet at https://
www.regulations.gov and https://
www.fws.gov/verobeach/. Comments
and materials we received, as well as
supporting documentation we used in
preparing this rule, are available for
public inspection at https://
www.regulations.gov. All of the
comments, materials, and
documentation that we considered in
this rulemaking are available by
appointment, during normal business
hours at: U.S. Fish and Wildlife Service,
South Florida Ecological Services
Office, 1339 20th Street, Vero Beach, FL
32960; telephone 772–562–3909.
FOR FURTHER INFORMATION CONTACT:
Roxanna Hinzman, Field Supervisor,
U.S. Fish and Wildlife Service, South
Florida Ecological Services Office, 1339
20th Street, Vero Beach, FL 32960, by
telephone 772–562–3909 or by facsimile
772–562–4288. Persons who use a
telecommunications device for the deaf
(TDD) may call the Federal Information
Relay Service (FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
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SUMMARY:
Executive Summary
Why we need to publish a rule. Under
the Act, a species may warrant
protection through listing if it is
endangered or threatened throughout all
or a significant portion of its range.
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Listing a species as an endangered or
threatened species can only be
completed by issuing a rule. This rule
will finalize the listing of the
Trichomanes punctatum ssp.
floridanum (Florida bristle fern) as an
endangered species.
The basis for our action. Under the
Act, we can determine that a species is
an endangered or threatened species
based on any of five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) Overutilization for
commercial, recreational, scientific, or
educational purposes; (C) Disease or
predation; (D) The inadequacy of
existing regulatory mechanisms; or (E)
Other natural or manmade factors
affecting its continued existence. We
have determined that the threats to
Trichomanes punctatum ssp.
floridanum consist primarily of
destruction and modification of habitat
(Factor A), proliferation of nonnative
invasive species, natural stochastic
events including hurricanes and tropical
storms, and impacts from climate
change including temperature shifts and
sea level rise (Factor E), and that
existing regulatory mechanisms have
not reduced or removed such threats
(Factor D).
Peer review and public comment. We
sought comments from independent
specialists to ensure that our
designation is based on scientifically
sound data, assumptions, and analyses.
We invited these peer reviewers to
comment on our listing proposal. We
also considered all comments and
information received during the
comment period.
Previous Federal Actions
Please refer to the proposed listing
rule for Trichomanes punctatum ssp.
floridanum (79 FR 61136), published on
October 9, 2014, for a detailed
description of previous Federal actions
concerning this subspecies.
Our proposed listing rule included a
finding that designation of critical
habitat was prudent, but that critical
habitat was not determinable. In this
final listing rule, we find that critical
habitat is still not determinable (see
Critical Habitat discussion below).
Background
Below we present updated and
revised information, based on peer
review and public comment received
during the comment period on the
proposed rule, as well as new
information, related to the subspecies’
life history, historical and current
ranges, and habitat requirements.
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Species Description
Trichomanes punctatum ssp.
floridanum, commonly referred to as the
Florida bristle fern, is mat-forming, has
root-like structures, and contains
trichomes (hairlike/bristlelike
outgrowths), which extend from soral
involucres (tubes containing sporangia
(an enclosure in which spores, or
reproductive cells, are formed)) on the
tips of some fronds (leaves of ferns)
when the plant is fertile (Wunderlin and
Hansen 2000, pp. 153–154). This
subspecies is very small in size and
superficially resembles bryophytes,
such as mosses and liverworts, making
it difficult to observe in its natural
habitat.
Wunderlin and Hansen (2000, pp.
153–154) described Trichomanes
punctatum ssp. floridanum as having
leaves, with the petiole (stalk by which
a leaf is attached to a plant) 0.1–2.0
centimeters (cm) (0.04–0.79 inches (in))
long and typically shorter than the
blade. The blade is fan-shaped, round,
entire or irregularly lobed at the apex,
and 0.5–2.0 cm (0.20–0.79 in) long and
0.2–1.1 cm (0.08–0.43 in) wide. T. p.
ssp. floridanum has thin veinlets (small
veins) that are not enlarged towards the
margin while true veins are uniform in
width to their apices (tips) (Nauman
1986, p. 179). This subspecies has few
false veins, and fronds are considered
simple (Morton 1963, p. 89).
One unusual characteristic of this
plant is that it lacks cuticles (the
protective layer that covers the
epidermis, which is the outermost layer
of cells that cover the leaves) or has
highly reduced cuticles. The fern has
differentiated epidermises and stomata
(small openings in leaves and stems
through which gases are exchanged),
causing it to be dependent on elevated
moisture conditions because a barrier is
not present to prevent unregulated loss
¨
of water (Kromer and Kessler 2006, p.
57). This dependence restricts most
Trichomanes ssp. to shaded areas
within forested environments with high
humidity, making them more vulnerable
to changes in localized climatic
conditions (Schuster 1971, p. 91;
Nauman 1986, pp. 181–182; van der
Heiden 2014, p. 5).
Taxonomy
The genus Trichomanes contains
approximately 320 species of ferns that
occur primarily in the tropics and for
which we generally lack ecological
information (Nauman 1986, p. 179;
Nelson 2000, p. 77). The genus belongs
to the family Hymenophyllaceae and the
hymenophylloid clade, where ferns are
also referred to as filmy ferns, which
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describes the thin, filmy leaves of the
species (Nelson 2000, p. 77). The
common name, bristle fern, is used to
reference the bristlelike structure that
singularly protrudes from each soral
involucre (a structure that holds and
produces spores) (Nelson 2000, p. 77).
Five species commonly known as
bristle ferns (Trichomanes ssp.) have
¨
been found in Florida (Kromer and
Kessler 2006, p. 57). Trichomanes
punctatum ssp. floridanum is a
subspecies of Trichomanes punctatum,
the current taxonomy of which is the
result of monographic revision of
Trichomanes sections (a taxonomic rank
or position below the genus but above
the species) Didymoglossum and
Microgonium by Wessels Boer (1962,
pp. 300–301). All U.S. species of
Trichomanes now belong to the section
Didymoglossum, except T. boschianum
(Morton 1963). Wessels Boer, in
reviewing specimens from throughout
the American tropics, determined that
all Trichomanes punctatum plants in
Florida represented the same taxon, not
two separate species, and that T.
sphenoides (which he described as T.
punctatum ssp. sphenoides) does not
occur in Florida. He further determined
that Trichomanes punctatum plants in
Florida were different from those in the
tropics and described them as a new
subspecies, Trichomanes punctatum
ssp. floridanum (Boer 1962, pp. 300–
301). This treatment has been followed
by almost all subsequent authors (Lakela
and Long 1976, p. 53; Wunderlin 1982,
p. 32; Lellinger 1985, p. 205; Nauman
1986, p. 181; Flora of North America
Editorial Committee 1993, p. 196;
Wunderlin 1998, p. 44; Nelson 2000, p.
81; Wunderlin and Hansen 2000, p. 153;
Wunderlin and Hansen 2003, p. 44).
The only exception is Long and Lakela
(1971, p. 73), who treated the subspecies
as T. punctatum without further
explanation. Additionally, the following
entities use the name T. p. ssp.
floridanum and indicate that this
subspecies’ taxonomic standing is
accepted:
• Florida Department of Agriculture
and Consumer Services (2013, https://
www.flrules.org/gateway/
RuleNo.asp?title=PRESERVATION%20
OF%20NATIVE%20FLORA%
20OF%20FLORIDA&ID=5B-40.0055),
• The Integrated Taxonomic
Information System (2011, p. 1),
• NatureServe (2013, https://
explorer.natureserve.org/servlet/
NatureServe?loadTemplate=tabular_
report.wmt&paging=home&
save=all&sourceTemplate=
reviewMiddle.wmt),
• The online Atlas of Florida
Vascular Plants (Wunderlin and Hansen
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2008, (https://
www.florida.plantatlas.usf.edu/
Plant.aspx?id=1122),
• The Flora of North America
(https://www.efloras.org/
florataxon.aspx?flora_id=1&taxon_
id=233501316), and
• The Florida Natural Areas
Inventory (FNAI) (FNAI, 2013, https://
fnai.org/trackinglist.cfm).
In summary, there is consensus that
Trichomanes punctatum ssp.
floridanum is a distinct taxon.
Currently there are two extant
metapopulations (groups of spatially
separated populations) of this
subspecies (Gann et al. 2002, pp. 552–
554), comprising four populations in
Miami-Dade County and two in Sumter
County, separated by a distance of
approximately 400 kilometers (km) (249
miles (mi)). As noted by Small (1938, p.
50), the Sumter metapopulation is a
considerable distance from where T. p.
ssp. floridanum was first discovered
(i.e., south Florida) and resides in a
climate and habitat unlike the MiamiDade County metapopulation. These
differences are likely why Morton (1963,
p. 90) suggested that the previous
determination of these two
metapopulations be reviewed. In March
2014, the Service contracted researchers
from Florida Atlantic University to
determine if the two metapopulations
were the same subspecies. Samples
were collected from both
metapopulations for genetic analysis.
DNA was isolated from the samples, and
sequencing was completed on five
samples from each metapopulation.
Researchers found no observable
differences in the sequence between the
five samples collected from Miami-Dade
County and the five samples from
Sumter County, indicating that both
metapopulations are the same
subspecies (Hughes 2014, pp. 1–4).
Life History
The life cycle of ferns is not
commonly understood (Possley 2014c,
pers. comm.). Information about the
specific life cycle of T. p. ssp.
floridanum is also lacking. Like all
ferns, this taxon has two life-history
stages, a gametophyte stage and a
sporophyte stage, and only the
sporophyte form is recognizable in the
wild, while the gametophyte form is
very cryptic (Possley 2013a, pers.
comm.; van der Heiden 2013b, pers.
comm.). Therefore, all reported
populations of Trichomanes punctatum
ssp. floridanum have been in the
sporophyte stage.
Mature plants can reproduce sexually
or asexually. The initial stage, when a
spore germinates, is referred to as the
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gametophyte stage. The gametophyte
contains separate sperm and eggproducing structures. In the presence of
water or moisture, sperm reach the eggs
for fertilization. Fertilized eggs, under
the proper conditions, develop into
sporophytes. The sporophytes produce
spores, which in turn can germinate to
produce new gametophytes (Nelson
2000, pp. 17–19). Reproduction may
also occur in one other way: By
division, when rhizomes (horizontal,
underground plant stems capable of
producing the shoot and root-like
structures of a new plant) break, forming
clones of the parent plant.
Although it has been suggested that
plants sporulate (produce spores)
mostly in the spring and summer
(Nauman 1986, p. 182), field
observations in Miami-Dade County
have observed sporangia in the months
of February, March, May, August,
October, and December. The plants are
likely fertile any time of year; however,
during the dry season, sporophytes have
been observed to desiccate and probably
do not produce spores (Possley 2013d,
pers. comm.). In Sumter County,
sporangia have been observed from
April through September; however,
researchers suggest they are likely
producing all year, with peaks in the
wet season (van der Heiden 2013c, pers.
comm.). For Trichomanes punctatum
ssp. floridanum, specific reproductive
and growth requirements, such as
moisture levels needed for each stage of
its life history, plant longevity, growth
rates, recruitment rates, dispersal
methods, and genetic variation, are
currently unknown.
Organizations such as the Institute for
Regional Conservation (IRC) and
Fairchild Tropical Botanic Garden
(Fairchild) are working together to
understand the biology and life history
of Trichomanes punctatum ssp.
floridanum. In 2002, IRC and Fairchild
collaborated with fern culture experts
from Marie Selby Botanical Gardens
(MSBG) in Sarasota, Florida, and tissue
culture experts at the Lindner Center for
Conservation and Research on
Endangered Wildlife (CREW) in
Cincinnati, Ohio (Gann et al. 2009, pp.
35–36). Currently, Fairchild maintains
fewer than five healthy clusters of T. p.
ssp. floridanum from plants obtained in
local hammocks (tropical hardwood
forests) that are monitored by their
organization. The success of this effort
to grow healthy T. p. ssp. floridanum
has yet to be determined due to several
factors, including: Slow growth rates,
the formation of unusual linear fronds,
the susceptibility to mold, and the lack
of sporulation (Possley et al. 2013, pp.
43–45). However, researchers at CREW
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have recently developed a successful
method to culture T. p. ssp. floridanum
in-vitro and cryopreserve (to preserve by
freezing at low temperatures)
sporophytes (V. Pence, submitted; Pence
and Charls 2006, pp. 29–34). The new
plants from CREW have recently been
transferred to MSBG, and plans are
under way to establish T. p. ssp.
floridanum onto limestone rock, which
could potentially be transferred to
solution hole (see description under
‘‘Habitat’’ section, below) walls for
eventual reintroduction to the wild
(Holst 2014, pers. comm.).
It is important to note that the
numerous efforts to cultivate
Trichomanes punctatum ssp.
floridanum ex-situ for possible future
reintroduction have been only partially
successful. Researchers have not been
able to propagate T. p. ssp. floridanum
via sexual reproduction. Although they
have been able to maintain the
subspecies in cultivation in the
greenhouse for several months at a time,
and temporarily establish rhizome
growth onto limestone rock, the
propagated fern eventually declines or
becomes overrun with mosses. Even
when there is vegetative growth, there is
no sign of spore production (Holst 2014,
pers. comm.).
Habitat
In southeastern North America,
Trichomanes ssp. are considered rare
because of their delicate nature and
requirements for deeply sheltered
habitats with almost continuous high
moisture and humidity (Farrar 1993, pp.
190–197; Zots and Buche 2000, p. 203),
restricting them from a more
widespread pre-glaciation distribution.
Trichomanes punctatum ssp.
floridanum is considered strongly
hygrophilous (growing or adapted to
damp or wet conditions) and generally
perceived as restricted to constantly
¨
humid microhabitat (Kromer and
Kessler 2006, p. 57). T. p. ssp.
floridanum occurs only in the United
States in the State of Florida. In Florida,
T. p. ssp. floridanum is known to occur
only in Miami-Dade and Sumter
Counties.
Both extant metapopulations occur in
dense canopy habitats, with shady
conditions that may be obligatory due to
the poikilohydric (i.e., possessing no
mechanism to prevent desiccation)
¨
nature of some fern species (Kromer and
Kessler 2006, p. 57). The canopy
directly contributes to the surrounding
humidity of an area. Dense canopies
found in rockland habitats can
minimize temperature fluctuations by
reducing soil warming during the day
and heat loss at night. In areas with
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greater temperature variations, as in
Sumter County, this temperature
minimization effect can help prevent
frost damage to the interior of the
hammock (FNAI 2010, p. 25). Mesic
conditions are further maintained by the
hammock’s rounded canopy profile,
which deflects winds, limiting
desiccation during dry periods and
reducing interior storm damage (FNAI
2010, p. 25). Changes in the canopy can
impact humidity and evaporation rates,
as well as the amount of light available
to the understory.
In Miami-Dade County, Trichomanes
punctatum ssp. floridanum is generally
epipetric (a plant that grows on rocks)
or epiphytic (a plant that grows nonparasitically upon another plant),
typically growing in rocky outcrops of
rockland hammocks, in oolitic
(composed of minute rounded
concretions resembling fish eggs)
limestone solution holes (see
description below), and, occasionally,
on tree roots in limestone-surrounded
areas (Phillips 1940, p. 166; Nauman
1986, p. 180; Whitney et al. 2004, pp.
105–106; Possley 2013e, pers. comm.;
van der Heiden 2014b, pers. comm.).
These rockland habitats are outcrops
primarily comprising marine limestone
representing the distinct geological
formation of the Miami Rock Ridge, a
feature that encompasses a broad area
from Miami to Homestead, Florida, and
narrows westward through the Long
Pine Key area of Everglades National
Park (ENP) (Snyder et al. 1990, pp. 233–
234). Several endemic plant species
have been identified to be closely
associated with the rocklands of
southern Florida; these plants are
believed to have no adaptation for longdistance dispersal, suggesting a lengthy
period of evolution on rocky substrate
in southern Florida (Snyder et al. 1990,
p. 236).
Rockland hammocks are a type of rich
tropical hardwood forest on upland sites
in areas where limestone is very near
the surface and often exposed. Once
numerous throughout South Florida,
these rockland hammocks have a
diverse closed canopy and shrub layer,
where more than 120 native tree and
shrub species are known to occur,
including a number of rare plant and
animal species, federally listed and
candidate species, South Florida
endemics, and tropical species at or
near the northern limit of their ranges
(Phillips 1940, p. 166; Snyder et al.
1990, p. 16; Gann et al. 2009, p. 3). The
forest floor is characterized by leaf litter
with varying amounts of exposed
limestone and has few herbaceous
species. Rockland hammocks generally
consist of larger, mature trees in the
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interior, while the margins can be
almost impenetrable due to dense
growth of smaller shrubs, trees, and
vines (FNAI 2010, pp. 24–27). The
canopy cover is typically very dense
where Trichomanes punctatum ssp.
floridanum occurs. In Miami-Dade
County, the hammocks consist of a mix
of temperate and tropical hardwood
trees, both canopy and understory,
including Ocotea coriacea (lancewood),
Coccoloba diversifolia (pigeon plum),
Quercus virginiana (live oak),
Simarouba glauca (paradise tree), Ficus
aurea (strangler fig), and Sideroxylon
foetidissimum (mastic) (see Snyder et al.
1990, p. 241, for complete list). Soils
where T. p. ssp. floridanum is extant in
Miami-Dade County generally consist of
an uneven layer of highly organic soil
overlying rock (Snyder et al. 1990, p.
238); soils are classified as Matecumbe
Muck (moderately well-drained soils
that are very shallow) (Florida
Geographic Data Library 2013, https://
www.fgdl.org/). Soils from historical and
extant records consist of the following
soil types: Krome Very Gravelly Loam,
Cardsound Silty Clay Loam-Rock
Outcrop Complex, Opalocka Sand-Rock
Outcrop Complex, and Dania Muck.
The limestone solution holes are
considered specialized habitat within
these hammock areas that host
Trichomanes punctatum ssp.
floridanum, as well as several other fern
species (Snyder et al. 1990, p. 247). The
solution hole features that dominate the
rock surface in the Miami Rock Ridge
are steep-sided pits, varying in size,
formed by dissolution of subsurface
limestone followed by a collapse above
(Snyder et al. 1990, p. 236). Limestone
solution holes vary in size, from shallow
holes less than 0.5 meter (m) (1.6 feet
(ft)) deep to those that cover over 100 m2
(1,076 ft2) and are several meters deep
(Snyder et al. 1990, p. 238). The bottoms
of most solution holes are filled with
organic soils, while deeper solution
holes penetrate the water table and have
(at least historically) standing water for
part of the year (Snyder et al. 1990, pp.
236–238). Humidity levels are higher in
and around the solution holes because
of standing water and moisture retained
in the organic soils. Many tropical,
epipetric plant species are associated
with the sinkholes and solution holes in
rockland hammocks.
In Sumter County, Trichomanes
punctatum ssp. floridanum is known to
be epipetric, residing on limestone
boulders in high atmospheric humidity
hammocks (van der Heiden 2013a, pers.
comm). The extant populations are
located in mesic hammocks on
limestone boulders 0.1–1.5 m (0.3–4.9
ft) tall (see ‘‘Current Range’’ section,
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below). Mesic hammock is a developed
evergreen hardwood and/or palm forest
on soils that are rarely inundated (FNAI
2010, pp. 19–23) and commonly
associated with hydric hammock and
mixed wetland hardwoods. The
difference between mesic hammocks
and surrounding habitats is a slight
difference in elevation. Mesic
hammocks occur on higher ground
within basin or floodplain wetlands; as
patches of oak/palm forest in dry prairie
or flatwoods communities; on river
levees; in ecotones (transition area
between two biomes or areas of distinct
plant and animal groups) between
wetlands and upland communities; and
at the edges of lakes, sinkholes, other
depressional or basin wetlands, and
river floodplains where natural fires do
not occur (FNAI 2010, pp. 19–23).
Recent field surveys (van der Heiden
2015a, p. 6; van der Heiden 2015b,
unpublished data; van der Heiden
2015c, unpublished data) have provided
additional information regarding
potential suitable habitat in Sumter
County. These surveys, conducted by
IRC and funded by the Service,
delineated suitable habitat within and
around the Jumper Creek Tract of the
Withlacoochee State Forest. Within
surveyed areas, IRC mapped all suitable
substrate found in areas having suitable
canopy and hydrology to support
growth of Trichomanes punctatum ssp.
floridanum. The resulting map included
limestone rocks and boulders in not
only mesic hammock, but also hydric
hammock, elevated hydric hammock,
and (in a small number of instances)
adjacent wetland (but non-hammock)
habitats. The Service is still evaluating
this information and working with IRC
to further refine suitable habitat
parameters for the fern in Sumter
County. Despite extensive surveys
through approximately 1,904 ha (4,705
ac) in and around the Jumper Creek
Tract, van der Heiden (2015a, p. 9) did
not find any new populations of T. p.
ssp. floridanum.
Although there are several
occurrences of Trichomanes punctatum
ssp. floridanum in Sumter County
where sunlight can be observed through
the canopy, generally the habitat is
shaded throughout the year, with the
lowest amount of canopy cover recorded
at approximately 65 percent (van der
Heiden and Johnson 2014, p. 20; in
Rocky Hammock). T. p. ssp. floridanum
has been observed growing on small
limestone rocks, as well as boulders
with tall, horizontal faces with
numerous other species, including rare
State-listed species (e.g., Asplenium
cristatum (hemlock spleenwort)) and
widespread Pecluma dispersa
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(widespread polypody) (van der Heiden
2013b, pers. comm.; van der Heiden and
Johnson 2014, pp. 15–16).
Within one occupied Sumter County
hammock (Rocky Hammock), the
majority of Trichomanes punctatum
ssp. floridanum occur on the northern
face of limestone boulders; however,
those clusters found on non-northfacing limestone generally occur in
close proximity to other boulders, trees,
or within protected crevices (van der
Heiden and Johnson 2014, p. 7). Van der
Heiden and Johnson (2014, pp. 9–10)
suggested that the northern aspect of
limestone boulders is more often
inhabited by this taxon because of the
reduced exposure to sunlight,
promoting cooler temperatures and
higher moisture as compared to other
sun-exposed sections of rock. This may
also be the case for those clusters
shielded by other boulders, by trees, or
in crevices, allowing the plant to grow
on any portion of the shielded rock as
long as moisture levels remain high
enough to prevent desiccation (van der
Heiden and Johnson 2014, pp. 9–10).
Additionally, both populations of T. p.
ssp. floridanum in Sumter County grow
within the northern quadrant of each
hammock.
Soils of mesic hammock are sands
mixed with organic matter, often
containing a thick layer of leaf litter and
generally well-drained. Although some
areas maintain high-moisture soils due
to the accumulation of leaf litter and
extensive canopy cover, in general,
mesic hammocks can occur across a
broad gradient of soil moisture
conditions, from somewhat xeric to
almost hydric soils. Rock outcrops may
also occur in mesic hammocks,
especially where limestone is near the
surface (FNAI 2010, pp. 19–23). Soil
types for the extant metapopulation of
Trichomanes punctatum ssp.
floridanum in Sumter County include
Okeelanta Muck, Frequently Flooded,
and Mabel Fine Sand (i.e., deep and
very deep, somewhat poorly drained,
slowly permeable soils that formed in
sandy to clayey marine deposits, with a
bouldery (abounding in rocks or stones)
subsurface and 0–5 percent slopes
(Florida Geographic Data Library 2013,
https://www.fgdl.org/)). Additionally,
one historical record has Adamsville
Fine Sand, Bouldery Subsurface, while
another population containing a
questionable record from an extirpated
population has what is classified as
Malabar Fine Sand, Frequently Flooded.
Plant communities associated with
mesic hammocks vary depending on the
latitude; tropical species gradually
increase in frequency from the central to
southern peninsular Florida. In south
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60443
Florida, some high-elevation areas dry
enough to support a semi-tropical mesic
hammock do exist; however, most ‘‘high
hammocks’’ are rockland hammocks
occurring on limestone (FNAI 2010, pp.
19–23). Q. virginiana is common in
mesic hammock communities. Oak
species found in these hammocks tend
to possess a broader tolerance of a range
of conditions than do oaks in other
habitats (FNAI 2010, pp. 19–23). Mesic
hammocks do not contain wetland trees,
as found in hydric hammocks; however,
these two hammock types often occur as
intermixed stands. Because mesic
hammocks are often associated with
hydric hammocks, with wetlands, or as
a transition to uplands, they are
sensitive to hydrologic alteration in the
landscape. For example, changes in
flooding frequency and/or duration can
kill most mesic hammock tree species,
while lowered water tables can shift
vegetation towards xeric species or
promote wildfires, destroying the
hammock (FNAI 2010, pp. 19–23).
Mesic hammocks may be distinguished
from rockland hammocks by the
dominance of temperate species in the
canopy, whereas rockland hammocks
are composed of predominantly tropical
woody species.
Trichomanes punctatum ssp.
floridanum in Sumter County can be
found under a dense canopy including
Q. virginiana, Sabal palmetto (cabbage
palm), Carpinus caroliniana (American
hornbeam), Celtis laevigata (sugarberry),
Acer negundo (boxelder), Liquidambar
styraciflua (sweetgum), and Sapindus
saponaria (wingleaf soapberry) (van der
Heiden 2013c, pers. comm.; van der
Heiden and Johnson 2014, p. 19). The
hammocks where T. p. ssp. floridanum
has been found are also surrounded by
a mosaic of wetlands dominated by
Taxodium distichum (cypress trees).
Field surveys of Sumter County
populations recorded 18 canopy species
in Rocky Hammock and 12 in Tree Frog
Hammock (van der Heiden and Johnson
2014, p. 19). The average canopy closure
for both populations in Sumter County
has been estimated to be more than 75
percent, where it is heavily shaded,
maintaining high humidity to reduce
chances of desiccation (van der Heiden
and Johnson 2014, p. 9). Van der Heiden
and Johnson (2014, p. 9) speculate this
dense, closed canopy can serve as a
shield for T. p. ssp. floridanum to
inhibit the growth of other plant species
on the same part of an inhabited rock
area.
Although it is believed this
subspecies needs high temperatures
(although likely not above 100 degrees
Fahrenheit (°F); Possley 2014c, pers.
comm.) and humidity, along with dense
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canopy, there is limited information on
optimal temperature and humidity
ranges or thresholds for Trichomanes
punctatum ssp. floridanum growth and
survival. In Miami-Dade County where
T. p. ssp. floridanum currently is found,
the mean maximum temperature from
2004 to 2013 was 29.0 degrees Celsius
(°C) (84.3 °F), and the mean minimum
temperature for the same time period
was 21.4 °C (70.5 °F) (https://
www1.ncdc.noaa.gov). In contrast,
yearly mean temperatures were lower
for Sumter County with 23.4 °C (74.2 °F)
recorded as the mean maximum
temperature from 2004 to 2013, and 11.8
°C (53.2 °F) as the mean minimum
temperature for the same time period
(National Oceanic and Atmospheric
Administration 2014, https://
www1.ncdc.noaa.gov).
Recent field studies have provided
some data on microhabitat conditions
(e.g., temperature and humidity) for
Trichomanes punctatum ssp.
floridanum populations in Sumter
County. Van der Heiden and Johnson
(2014, pp. 8, 21) found average relative
humidity to be around 95 percent in
both Rocky Hammock and Tree Frog
Hammock, while average ambient
temperature in both hammocks was
approximately 21 °C (70 °F) from
September 2013 to November 2013.
However, during cooler periods (19–21
°C; 66–70 °F) when humidity levels
dropped slightly (by approximately 2
percent), observed plant health
declined, demonstrating the fragile
nature of this taxon and its dependence
on high-humidity conditions (van der
Heiden and Johnson 2014, pp. 9, 21).
Collection of humidity and temperature
data within these same areas was
subsequently continued through March
2015. From September 2013 to March
2015, average monthly temperatures in
both hammocks were very similar and
ranged from approximately 12 °C (53 °F;
in January 2014) to 25 °C (78 °F; in
August 2014) (van der Heiden 2015a, p.
17). The average relative humidity in
both hammocks was 94.8 percent
throughout the study (van der Heiden
2015a, p. 5). This type of information
needs to be further explored to
determine habitat requirements (i.e.,
thresholds for humidity and
temperature) for both metapopulations
of this taxon.
Historical Range/Distribution
The historical range of Trichomanes
punctatum ssp. floridanum included
southern (Miami-Dade County; see
Table 1, below) and central (Sumter
County; see Table 2, below) Florida.
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Miami-Dade County
In Miami-Dade County, the historical
range of this subspecies extended from
its southern limit in Royal Palm
Hammock (now part of ENP) northeast
to Deering-Snapper Creek Hammock,
which includes the modern-day site of
Smather’s Four Fillies Farm residential
area, near R. Hardy Matheson Preserve
(derived from Gann et al. 2002, pp. 552–
554), a range of at least 45 square
kilometers (km2) (17 square miles (mi2)).
Plants in Miami-Dade were known to
historically occur in at least 11
hammocks: Deering-Snapper Creek
Hammock, Castellow Hammock, Silver
Palm Hammock (also known as
Caldwell), Ross Hammock, Royal Palm
Hammock (in ENP), Hattie Bauer
Hammock, Shields Hammock, NixonLewis Hammock, Fuchs Hammock,
Addison Hammock (in the Deering
Estate at Cutler), and Matheson
Hammock. In the 1980s, T. p. ssp.
floridanum was also documented in
Meissner Hammock and Cox Hammock
(now part of the tourist attraction
‘‘Monkey Jungle’’) (Small 1918, p. 6;
Small 1921, p. 211; Morton 1963 p. 90;
Fairchild Tropical Garden 1968, p. 1;
Nauman 1986 p. 182; Gann et al. 2002,
pp. 552–554; Gann 2013, https://
regionalconservation.org/ircs/database/
plants/IRCSpAccount.asp?
TXCODE=Tricpuncflor&
GENUS=Trichomanes&
SPECIES=punctatum&Author=Poir.&
INFRA1=subsp.&INFRA1NAME= ssp.
floridanum&INFRA1AUTHOR=
Wess.%20Boer&
CommonNames=Florida%20
bristle%20fern).
J.K. Small documented Trichomanes
punctatum ssp. floridanum in 1901 at
Deering-Snapper Creek. J.K. Small made
subsequent collections of the subspecies
in and around Miami-Dade County
including one in 1903, probably located
in or near present-day Castellow
Hammock (Gann 2014d, pers. comm.).
A.A. Eaton collected additional
specimens from Castellow Hammock in
1903. More recent observations of T. p.
ssp. floridanum in Castellow Hammock
include documentation by G. Gann and
K. Bradley in the late 1990s (Bradley
and Gann 1999), and subsequent
observations by J. Possley and others
(Gann et al. 2002, pp. 552–554; Possley
et al. 2013, pp. 43–45). T. p. ssp.
floridanum was collected by A.A. Eaton
in Silver Palm Hammock in 1903 and
reported again in 1980; however, the
1980 report was not confirmed. The fern
was collected from Ross Hammock by
J.K. Small and colleagues in 1906. Since
then, part of this hammock has been
damaged, and what remains is currently
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protected as a Miami-Dade County
Environmentally Endangered Lands
(EEL) Preserve. In 1909, the subspecies
was collected in Royal Palm Hammock
(also known as Paradise Key), now
within ENP, and later reported by W.E.
Stafford in 1917 (Stafford 1919, p. 386;
Gann et al. 2002, pp. 552–554).
Several collections of Trichomanes
punctatum ssp. floridanum were made
in Miami-Dade in 1915, including:
Hattie Bauer Hammock, Shields
Hammock, Nixon-Lewis Hammock,
Fuchs Hammock, and Deering-Snapper
Creek Hammock. Hattie Bauer
Hammock, now a Miami-Dade County
conservation area, has numerous
subsequent collection records by Small
(1915, 1916), Correll (1936), and
McFarlin (1934, 1940) as cited by Gann
2013, https://regionalconservation.org/
ircs/database/plants/
IRCSpAccount.asp?TXCODE=
Tricpuncflor&GENUS=Trichomanes&
SPECIES=punctatum&Author=Poir.&
INFRA1=subsp.&INFRA1NAME= ssp.
floridanum&
INFRA1AUTHOR=Wess.%20Boer&
CommonNames=Florida%20
bristle%20fern. The last known
collection in Hattie Bauer Hammock
was recorded in 1960, by T. Darling, Jr.
It was subsequently reported as
extirpated by Gann et al. (2002, pp. 552–
554), until it was rediscovered in this
hammock in 2011 by Possley (Possley et
al. 2013, pp. 1–2). Shields Hammock
was destroyed prior to 1991 (Cressler
1991, Handwritten Notes). Fuchs
Hammock is now part of the Fuchs
Hammock Preserve (Gann et al. 2002,
pp. 552–554), and the subspecies was
vouchered (pressed plant samples taken
for future reference) again in 1954, by L.
J. Brass; in 1959, by T. Darling Jr.; and
in 1969, by F.C. Craighead (The Institute
for Regional Conservation, Herbarium
Specimens, Floristic Inventory of South
Florida Database, September 12, 2007).
T. p. ssp. floridanum was also
vouchered in Fuchs Hammock in 1993,
following Hurricane Andrew (1992) by
A. Cressler (Cressler 12 February 1993,
handwritten notes), and it has been
more recently observed by Possley and
others over the years (Gann et al. 2002,
pp. 552–554; Possley et al. 2013, pp.
43–45). T. p. ssp. floridanum was
observed by G. N. Avery in 1983 in
Meissner Hammock (immediately
adjacent to Fuchs Hammock) and was
since vouchered by K. Bradley in 1997
and 2002 and also observed by others
(Gann et al. 2002, pp. 552–554; Possley
et al. 2013, pp. 43–45).
In 1916, J.K. Small reported
Trichomanes punctatum ssp.
floridanum in Addison Hammock, now
located within Deering Estate at Cutler,
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06OCR2
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currently Miami-Dade County Park;
however, these reports were never
vouchered (J.K. Small 1916; Gann et al.
2002, pp. 552–554). Surveys in recent
years have yet to find any populations
of T. p. ssp. floridanum in Deering
Estate at Cutler, Matheson Hammock, or
Silver Palm Hammock (Possley 2013i,
pers. comm.). The subspecies was last
reported from Cox Hammock in 1989,
by A. Cressler, where plants were
observed in a sinkhole in the tourist
attraction ‘‘Monkey Jungle’’ (Cressler
1991, handwritten notes); it is not
known if these plants still exist. Cox
Hammock is located about 1.6 km (1.0
mi) northeast of Castellow Hammock
Park. Additional hammocks existing
today where the taxon formerly
occurred include Ross and Royal Palm
Hammock (in ENP) and DeeringSnapper Creek Hammock. A section of
Deering-Snapper Creek Hammock was
destroyed in 1912–1913, when the
Snapper Creek Canal was constructed.
Dredging of this canal drastically altered
the water table in the area, depleting the
freshwater springs, while a large spoil
berm from excavation of the canal
destroyed habitat (Metro-Dade County
Park and Recreation Department 1991,
p. 10). Other hammocks in the historical
60445
range that are presumed destroyed
include Nixon Lewis Hammock, which
is partially destroyed (Gann 2013,
https://regionalconservation.org/ircs/
database/plants/
IRCSpAccount.asp?TXCODE=
Tricpuncflor&GENUS=Trichomanes&
SPECIES=punctatum&Author=
Poir.&INFRA1=subsp.&INFRA1NAME=
ssp. floridanum&
INFRA1AUTHOR=Wess.%20Boer&
CommonNames=Florida%
20bristle%20fern) and a station
presumably near the Matheson
Hammock Park vouchered by G.
Peterson in 1940.
TABLE 1—SUMMARY OF HISTORICAL REPORTS AND CURRENT POPULATION AND HAMMOCK STATUS OF EACH
TRICHOMANES PUNCTATUM SSP. FLORIDANUM LOCATION IN MIAMI-DADE COUNTY
[Gann et al. 2002; The Institute for Regional Conservation, Herbarium Specimens, Floristic Inventory of South Florida Database, September 12,
2007; Florida Natural Areas Inventory element occurrences 9/12/2013; Possley 2013c, i–j, 2014a–c; Possley 2013, 2014a pers. comm.;
Gann 2013, pers. comm.; van der Heiden 2013e, pers. comm.; Gann 2014a–f, pers. comm.; Gann et al. 2001–2014). Population locations
(hammocks) are numbered in chronological order by T. p. ssp. floridanum initial discovery date.]
Number of
specimens
collected
Current
population
status
Current
hammock status
Extirpated
Protected Area, Partially Destroyed.
2
Extant ......
Protected Area.
4
1
2
Extirpated
Extirpated
2
Extirpated
Protected Area.
Protected Area, Partially Destroyed.
Protected Area.
1
Extant ......
Protected Area.
2
2
1
1
1
Extirpated
Destroyed.
1
Extirpated
1
Extant ......
Protected Area, Partially Destroyed.
Protected Area.
Year(s) of
initial report(s)
Population location
1 ...................
Deering-Snapper Creek Hammock-Smather’s Four Fillies
Farm (R. Hardy Matheson
Preserve).
Observer
1901
J.K. Small, G.V.
Nash.
3
1915
No.
J.K. Small, C.A.
Mosier.
J.K. Small, J.J. Carter.
A.A. Eaton ................
A.A. Eaton ................
J.K. Small, J.J. Carter.
J.K. Small, J.J. Carter.
W.E. Stafford ............
J.K. Small, C.A.
Mosier.
J.K. Small .................
J.K. Small, C.A.
Mosier, G.K. Small.
J.K. Small .................
1
2 ...................
Castellow Hammock ..................
1903
3 ...................
4 ...................
Silver Palm Hammock ...............
Ross Hammock ..........................
1903
1903
1906
5 ...................
Royal Palm Hammock (ENP);
aka Paradise Key.
1909
1917
1915
1915
1915
6 ...................
Hattie Bauer Hammock (Orchid
Jungle).
1916
7 ...................
Shields Hammock ......................
1934
1936
1940
1960
1915
8 ...................
Nixon-Lewis Hammock ..............
1915
9 ...................
Fuchs Hammock (Sykes Hammock).
1915
3
5
1916
11 .................
Deering
Estate
at
Cutler
(Addison Hammock).
Matheson Hammock Park .........
J.B. McFarlin ............
D.S. Correll ...............
J.B. McFarlin ............
T. Darling Jr. .............
J.K. Small, C.A.
Mosier, G.K. Small.
J.K. Small, C.A.
Mosier.
J.K. Small, C.A.
Mosier.
L.J. Brass .................
T. Darling Jr. .............
A.F. Clewell, F.C.
Craighead.
J.K. Small .................
1940
G. Peterson ..............
2
12 .................
13 .................
Meissner Hammock ...................
Monkey Jungle (Cox Hammock)
1983
1989
G.N. Avery ................
A. Cressler ................
None
None
1954
1959
1969
10 .................
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None
2
1
1
1
None
Unconfirmed 1.
Unconfirmed 2.
Extant ......
Unknown 3
1 Initial
report is questionable.
location of sample and associated report is questionable.
3 It is not known whether the subspecies still occurs here.
2 Precise
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Protected Area.
Protected Area.
Protected Area.
Privately Owned,
Partially Destroyed.
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Sumter County
In Sumter County, early collections
and herbarium label data for
Trichomanes punctatum ssp.
floridanum are not accurate or precise
in their location descriptions. The first
documented collection in 1936, by R.P.
St. John, simply states that T. p. ssp.
floridanum was found 11.26 km (7.0 mi)
east of Floral City. This collection is
close to the extant populations in
Sumter (in Rocky Hammock within
Withlacoochee State Forest), which is
east-southeast of Floral City, and is
thought to be the location where T. p.
ssp. floridanum existed on private land
until it was cleared for cattle sometime
after 1983. A specimen found 3 years
later, by J.B. McFarlin in 1939, was
originally thought to be T. sphenoides;
the herbarium label data described this
collection as ‘‘South of Floral City,
Florida. T. sphenoides is a misapplied
synonym for T. p. ssp. floridanum
according to FNAI. This is the only
known station in the United States.’’ It
is believed that these label data may
have been incorrectly recorded,
indicating a direction of south from
Floral City, when it should have been
east. In all likelihood, McFarlin’s
collection probably referred to the
population in the Wahoo area, where St.
John previously collected because he
states his collection was from the same
locality where it was originally found in
1936. The specimen found by McFarlin
eventually led to reports of the taxon in
Citrus County (Wherry 1964, p. 232;
Nelson 2000, p. 81); however, this was
never confirmed beyond the initial
report. Systematic surveys have not
been conducted in Citrus County;
therefore, the only documented
occurrences of T. p. ssp. floridanum in
this region of Florida have been in
Sumter County, just north of Wahoo and
east of the Withlacoochee River.
Several years later, in 1954, R. Garrett
collected Trichomanes punctatum ssp.
floridanum southeast of Floral City. It is
thought to be the same location where
St. John and McFarlin made their
previous collections; however, label
data were again minimal and the exact
location is uncertain. In 1959, T. Darling
Jr. found this subspecies near Floral
City, 11.26 km (7.0 mi) south near a
location called Battle Slough. This
record has never been confirmed
because it is located on private property.
Another specimen was found in 1963,
by O. Lakela in an area known as Indian
Field Ledges. Lakela recorded his
location and collection to be west of
Withlacoochee River off State Road #48.
This information is believed to be
incorrect based on a site visit by Darling
(1961, p. 7), stating that the Indian Field
Ledges is north of Wahoo, a locality east
of the Withlacoochee River. T. p. ssp.
floridanum was not found again in
Sumter County until 1983, when SW.
Leonard made a collection on private
property known as Rocky Point, north of
Wahoo. This is presumed to be the same
location where St. John, McFarlin, and
Garrett collected their specimens. This
population is now extirpated.
TABLE 2—SUMMARY OF PRESUMED EXTIRPATED, EXTIRPATED, AND UNCONFIRMED TRICHOMANES PUNCTATUM SSP.
FLORIDANUM POPULATIONS IN SUMTER COUNTY
[Gann et al. 2002; The Institute for Regional Conservation, Herbarium Specimens, Floristic Inventory of South Florida Database, September 12,
2007; Florida Natural Areas Inventory Element Occurrences 9/12/2013; van der Heiden 2013d, 2014a, pers. comm.; Gann et al. 2001–
2014). Population locations (hammocks) are numbered in chronological order by T. p. ssp. floridanum initial discovery date.]
No.
Population location
1 ................
Year of initial
report
11.26 km (7 mi) East
of Floral City 1.
Floral City Area 1 ........
Southeast of Floral
City 1.
Floral City, 11.26 km
(7 mi) south (Battle
Slough) 1.
East of Withlacoochee
River, off State
Road #48 (Indian
Field Ledges) 1.
Rocky Point, (north of
Wahoo).
2 ................
3 ................
4 ................
5 ................
6 ................
Number of
specimens
collected
Observer
Current
population status
Current
hammock status
Privately Owned, Presumed Destroyed.
Unknown.
Privately Owned, Presumed Destroyed.
Privately Owned, Unknown.
1936
R.P. St. John ..............
1
Presumed Extirpated ..
1939
1954
J.B. McFarlin ..............
R. Garret ....................
1
1
Unconfirmed 2 .............
Presumed Extirpated ..
1959
T. Darling Jr. ..............
1
Unconfirmed 2 .............
1963
O. Lakela ....................
1
Extirpated ...................
Protected Area.
1983
S.W. Leonard .............
1
Extirpated ...................
Privately Owned, Destroyed.
1 Sumter
2 Initial
County collections and herbarium label data for Trichomanes punctatum ssp. floridanum are inaccurate in location descriptions.
report is questionable.
Current Range
The extant metapopulation of
Trichomanes punctatum ssp.
floridanum in Miami-Dade County is
approximately 400 km (249 mi) south of
the extant metapopulation in Sumter
County. Both metapopulations of T. p.
ssp. floridanum are located entirely on
public lands (see Table 3, below). In
general, Trichomanes punctatum ssp.
floridanum occurs in small areas within
each hammock.
TABLE 3—SUMMARY OF KNOWN EXTANT OCCURRENCES OF TRICHOMANES PUNCTATUM SSP. FLORIDANUM.
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[Possley 2013, pp. 1–2; Dozier 2014, Pers. Comm.; van der Heiden and Johnson 2014, pp. 5, 26]
Metapopulation
location
(county)
Population location
Land ownership
Miami-Dade .........................
Miami-Dade .........................
Miami-Dade .........................
Meissner Hammock ....................................................
Fuchs Hammock Preserve. ........................................
Castellow Hammock Park ..........................................
State .................................
County ..............................
County ..............................
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06OCR2
Number of
subpopulations
Status
2
4
3
Extant.
Extant.
Extant.
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Federal Register / Vol. 80, No. 193 / Tuesday, October 6, 2015 / Rules and Regulations
TABLE 3—SUMMARY OF KNOWN EXTANT OCCURRENCES OF TRICHOMANES PUNCTATUM SSP. FLORIDANUM.—Continued
[Possley 2013, pp. 1–2; Dozier 2014, Pers. Comm.; van der Heiden and Johnson 2014, pp. 5, 26]
Metapopulation
location
(county)
Miami-Dade .........................
Sumter .................................
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Sumter .................................
Land ownership
Hattie Bauer Hammock ..............................................
Rocky Hammock, Withlacoochee State Forest’s
Jumper Creek Tract.
Tree Frog Hammock, Withlacoochee State Forest’s
Jumper Creek Tract.
County ..............................
State .................................
1
1
Extant.
Extant.
State .................................
1
Extant.
Miami-Dade County
The four populations that constitute
the Miami-Dade County metapopulation
are located in urban preserves managed
by the County’s EEL Program and the
Natural Areas Management (NAM)
Division of Miami-Dade County’s Parks,
Recreation and Open Spaces (PROS)
Department (see Factor A, Conservation
Efforts to Reduce Habitat Destruction,
Modification, or Curtailment of Its
Range, below). These EEL Preserves
include: Castellow Hammock Park (39.5
hectares (ha)) (97.6 acres (ac)), Hattie
Bauer Hammock (5.7 ha (14.0 ac)),
Fuchs Hammock Preserve (15.7 ha (38.8
ac)), and Meissner Hammock (4.1 ha
(10.1 ac)). Three of these preserves (76
percent of the land area) are owned by
the County; the fourth, Meissner
Hammock (24 percent), is owned by the
State and leased to the County (Dozier
2014, pers. comm.). The population in
Fuchs Hammock Preserve includes a
new subpopulation that was found in
July 2013 (Possley et al. 2013, pp. 43–
45). Fuchs and Meissner Hammocks are
immediately adjacent to each other, and
Castellow Hammock Park is 10.5 km
(6.5 mi) to the northeast. Although the
fern was thought to be extirpated from
Hattie Bauer Hammock in 1960, another
population was re-discovered there in
2011 (8 ha (20 ac)) (Possley et al. 2013,
pp. 43–45). Hattie Bauer Hammock is
4.02 km (2.5 mi) south of Castellow
Hammock and approximately 8.05 km
(5 mi) northeast of Fuchs and Meissner
Hammocks.
No comprehensive survey has been
conducted in rockland hammocks in
Miami-Dade County where suitable
Trichomanes punctatum ssp.
floridanum habitat has been identified.
Although these areas have been
extensively explored by numerous
botanists and plant enthusiasts,
including sites where the subspecies
was formerly found, due to the cryptic
nature of this plant it may have been
overlooked and new occurrences may
yet be discovered (Possley 2013e, pers.
comm.; van der Heiden 2013c, pers.
comm.). Surveys conducted in the late
1990s, and as late as 2010, did not find
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Number of
subpopulations
Population location
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T. p. ssp. floridanum in Silver Palm
Hammock (Gann et al. 2002, pp. 552–
554; Possley 2013f, pers. comm.). A
sporophyte sample was collected in
Nixon-Lewis Hammock by Small and
Mosier in 1915; however, due to
extensive disturbance of this hammock,
subsequent surveys conducted in 2006,
by IRC, could not find the taxon
(Bradley and Gann 2005, unpublished
data). Over the years, IRC has completed
systematic surveys in ENP in Royal
Palm Hammock and other hammocks on
Long Pine Key (also in ENP); however,
sporophytes have not been found there
(Gann et al. 2009; pp. 1–66). In 2003,
based on historical records, staff from
ENP and IRC surveyed Royal Palm
Hammock for T. p. ssp. floridanum
without success; subsequent surveys
conducted in rockland hammocks
throughout Long Pine Key for other rare
plants also were not successful in
finding T. p. ssp. floridanum (Sadle
2013, pers. comm.).
Sumter County
The Sumter County metapopulation
consists of two extant populations of
Trichomanes punctatum ssp.
floridanum that have been reported
north of Wahoo, in the Withlacoochee
State Forest’s Jumper Creek Tract; these
populations are located in Rocky
Hammock (located on 44 boulders) and
Tree Frog Hammock (located on 4
boulders) (van der Heiden and Johnson
2014, p. 7). The population in Tree Frog
Hammock was discovered as recently as
April 2013, during regional surveys (van
der Heiden 2013c, pers. comm.). Two
additional populations were known
from private land just south of the State
Forest; however, these populations were
subsequently extirpated due to the
clearing of land for agriculture by the
property owner (van der Heiden 2013c,
pers. comm.).
Recent GIS analyses show the soil
type associated with known extant
occurrences of Trichomanes punctatum
ssp. floridanum in the northern
metapopulation to be Okeelanta Muck,
Frequently Flooded; this soil covers
approximately 1,478 ha (3,652 ac) in
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Status
Sumter County. However, not all of
these areas have been systematically
surveyed. Surveys were conducted of a
boulder field within Withlacoochee
State Forest’s Jumper Creek Tract (called
the Indian Field Ledges) in August 2007
and April 2013 and were unsuccessful
(van der Heiden 2013c, pers. comm.).
The discovery of new populations may
be possible in the area. Indeed, the
population of this subspecies in Jumper
Creek’s Tree Frog Hammock is a new
population that was discovered in April
2013, during additional hammock
surveys within Withlacoochee State
Forest and the surrounding area (van
der Heiden 2013c, pers. comm.).
However, IRC recently conducted
extensive surveys through
approximately 1,904 ha (4,705 ac) in
and around the Jumper Creek Tract, and
no additional populations of T. p. ssp.
floridanum were located (van der
Heiden 2015a, p. 9).
It is also possible that other
subpopulations may exist in Sumter
County. Indian Ledges, a hammock
located on private land near Jumper
Creek (not to be confused with Indian
Field Ledges), just north of Wahoo, is
believed to be suitable for Trichomanes
punctatum ssp. floridanum, including a
dense canopy and appropriate soil
(Deangelis 2014a–b, pers. comm.). Over
the years, many rare ferns and orchids
have been observed in the Indian Ledges
Hammock; unfortunately, this hammock
was heavily damaged by hurricanes in
2004 (Deangelis 2014a, pers. comm.).
Portions of the Southwest Florida
Water Management District (SWFWMD)
property within the Green Swamp, more
than 40.23 km (25 miles) southeast of
the Jumper Creek Tract in
Withlacoochee State Forest, may also
contain appropriate habitat for
Trichomanes punctatum ssp.
floridanum based on existing habitat
features such as dense canopy, high
humidity microclimates, mesic
hammock, and limestone outcroppings
(Elliott 2014, pers. comm.). The
SWFWMD property within the Green
Swamp is the only area where land
alteration has not occurred in Sumter
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County (11,343 ha (28,030 ac)). Portions
of Green Swamp owned by the
SWFWMD also extend into three other
counties: Lake, Polk, and Pasco. Future
survey efforts, coordinating with local
land owners and conservation
organizations in this area, may prove
successful in finding new populations
of T. p. ssp. floridanum.
Population Estimates and Status
Trichomanes punctatum ssp.
floridanum grows in dense mats and is
rhizomatous (a horizontal stem that
often sends out root-like structures from
its nodes). Fronds are scattered in
matted clusters along the stems, making
it difficult to count clusters, or groups
of plants in the same location, and
nearly impossible to accurately count
individual plants (Nelson 2000, p. 79).
This issue has been encountered in
other Trichomanes species, such as
Trichomanes boschianum (Appalachian
bristle fern) (Hill 2003, p. 11). As such,
populations are typically described by
the number of clusters (i.e., groups of
plants in various sinkholes, on tree
roots, on boulders) and the total area
covered by the cluster.
Miami-Dade County
In Miami-Dade County, there are four
populations of the fern with a total of 10
subpopulations (i.e., nine solution holes
and one rocky outcropping on a tree
root). Overall, this taxon occurs in small
areas (i.e., less than 0.5 ha (1.2 ac)) at
each site, with 88 percent of the total
area in three subpopulations in
Castellow Hammock. Recent surveys
(see Table 4, below) in Miami-Dade by
Fairchild (Possley 2013, pp. 1–2) found
the fern covering a total area of
approximately 9.92 m2 (106.56 ft2)
(Possley 2013, pp. 1–2).
TABLE 4—AREA COVERED BY EACH OF 10 KNOWN SUBPOPULATIONS OF TRICHOMANES PUNCTATUM SSP. FLORIDANUM IN
MIAMI-DADE COUNTY, OCTOBER AND NOVEMBER 2013
[(Possley 2013, pp. 1–2) and in Sumter County, December 2013 (van der Heiden and Johnson 2014, pp. 7, 14)]
Metapopulation
Estimated area
covered
(m2)
Number of
clusters
Population
Subpopulation
.........................................
.........................................
.........................................
.........................................
.........................................
.........................................
.........................................
.........................................
.........................................
.........................................
Hattie Bauer Hammock ......................
Fuchs Hammock ................................
Fuchs Hammock ................................
Fuchs Hammock ................................
Fuchs Hammock ................................
Meissner Hammock ...........................
Meissner Hammock ...........................
Castellow Hammock ..........................
Castellow Hammock ..........................
Castellow Hammock ..........................
Hole (no tag) ..................
Hole 532 ........................
Hole 533 ........................
Hole 1431 ......................
Root 1430 ......................
Hole 2319 ......................
Hole 3337 ......................
Hole 2332 ......................
Hole 2331 ......................
Hole 944 ........................
0.078
0.017
0.038
0.128
0.047
0.145
0.713
4.688
3.925
0.141
2–10
2–10
2–10
2–10
1
2–10
2–10
11–100
11–100
2–10
Miami-Dade County Total ............
Sumter ................................................
Sumter ................................................
............................................................
Rocky Hammock ................................
Tree Frog Hammock ..........................
........................................
N/A .................................
N/A .................................
9.920
4.355
0.132
........................
44
4
Sumter County Total ...................
............................................................
........................................
4.487
........................
TOTAL Area Covered ..................
............................................................
........................................
14.407
........................
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Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
Miami-Dade
The largest known population of
Trichomanes punctatum ssp.
floridanum in Miami-Dade County is
located at Castellow Hammock (Possley
et al. 2013, p. 43), where it occurs in
three of the larger subpopulations. In
October of 2011, field surveys revealed
extensive desiccation of this population
after intensive nonnative vegetation
removal (Possley 2013g, pers. comm.);
however, by November 2013, these
plants had recovered, and the total area
covered by all clusters (i.e., two or more
plants next to each other) was estimated
at 8.754 m2 (94.227 ft2). Meissner
Hammock has two subpopulations; the
clusters in this hammock cover an area
of 0.858 m2 (9.235 ft2) and are
considered healthy, with no signs of
desiccation (Possley et al. 2013, pp. 43–
45). There is one subpopulation in
Hattie Bauer Hammock covering
approximately 0.78 m2 (8.4 ft2), and
three subpopulations of T. p. ssp.
floridanum at Fuchs Hammock, with an
additional one that was discovered in
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Sumter County
In Sumter County, the Rocky
Hammock subpopulation contains 44
clusters, while the newly discovered
subpopulation (Tree Frog Hammock) is
much smaller with only 4 clusters
observed (van der Heiden and Johnson
2014, p. 7). Average cluster size for
Rocky Hammock is estimated at 4.355
m2 (46.877 ft2) and 0.132 m2 (1.421 ft2)
for Tree Frog Hammock.
comment on the proposal. Newspaper
notices inviting general public comment
were published in the Miami Herald.
We did not receive any requests for a
public hearing. All substantive
information provided during comment
periods has either been incorporated
directly into this final determination or
addressed below.
Peer Reviewer Comments
July 2013, totaling an area of 0.230 m2
(2.476 ft2) (Possley 2013, pp. 1–2;
Possley et al. 2013, pp. 43–45).
Summary of Comments and
Recommendations
In the proposed rule published on
October 9, 2014, we requested that all
interested parties submit written
comments on the proposal by December
8, 2014. We also contacted appropriate
Federal and State agencies, scientific
experts and organizations, and other
interested parties and invited them to
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In accordance with our peer review
policy published on July 1, 1994 (59 FR
34270), we solicited expert opinion
from five knowledgeable individuals
with scientific expertise that included
familiarity with Trichomanes
punctatum ssp. floridanum and its
habitat, biological needs, and threats.
We received responses from all five of
the peer reviewers.
We reviewed all comments received
from the peer reviewers for substantive
issues and new information regarding
the listing of Trichomanes punctatum
ssp. floridanum. The peer reviewers
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generally concurred with our methods
and conclusions and provided
additional information, clarifications,
and suggestions to improve the final
rule.
(1) Comment: One peer reviewer
noted that he was unaware of any
documentation that Trichomanes
punctatum ssp. floridanum formed
gemmae, as stated in the proposed rule.
He commented that the works cited
were in reference to other species of
Trichomanes and Hymenophyllaceae, in
general. Also, the peer reviewer pointed
out a reference (Hughes 2014) in the
proposal that the two metapopulations
have no observable genetic differences.
The peer reviewer noted that, in the Life
History section, the proposal states
many traits of the subspecies, such as
‘‘genetic variation,’’ are unknown,
which contradicts the data from Hughes.
Our Response: We appreciate this
information and have corrected and
updated the rule as follows: (1) We
removed the phrase that stated
Trichomanes punctatum ssp.
floridanum produces gemmae; and (2)
the term genetic variation has been
removed from a sentence discussing
specific reproductive and growth
requirements that are unknown for the
subspecies, as it conflicted with
previous information within the
proposed rule.
(2) Comment: Two peer reviewers
noted that, under the Species
Description section, the proposed rule
incorrectly compares physical
characteristics of Trichomanes
punctatum ssp. floridanum with ‘‘other
bryophytes.’’ The phrase should only
read ‘‘bryophytes,’’ not ‘‘other
bryophytes.’’
Our Response: The word ‘‘other’’ has
been deleted from the text within the
Species Description section because
Trichomanes punctatum ssp.
floridanum is a fern and not a
bryophyte.
(3) Comment: One peer reviewer
noted, under the Life History section,
that although it is true that the
sporophyte form is recognizable and
spores are invisible to the naked eye,
that sentence does not align with the
previous thought in the paragraph that
there are two stages, a sporophyte and
a gametophyte stage.
Our Response: We have restructured
the sentence and noted that the
gametophyte form is cryptic and
invisible to the naked eye.
(4) Comment: One peer reviewer
questioned why the two extant
populations in Sumter County (that are
listed in Table 3) are not listed in Table
2.
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Our Response: Table 2 is a composite
of populations that are presumed
extirpated, extirpated, or unconfirmed
(where the report was questionable).
Table 3 is a summary of the known
extant occurrences of Trichomanes
punctatum ssp. floridanum. The title of
Table 2 has been modified for clarity in
the final rule.
(5) Comment: One peer reviewer
noted that numerous efforts to cultivate
Trichomanes punctatum ssp.
floridanum ex-situ for possible future
reintroduction have only been partially
successful and provided information on
ex-situ reproduction efforts. The
reviewer noted that, given the problems
with ex-situ reproduction, it is critical
the extant wild populations be protected
to the greatest extent possible.
Our Response: We have added text
explaining propagation challenges and
the importance of protecting extant
populations in the wild.
Comments From the State
We received one comment from the
Florida Natural Areas Inventory
regarding a discrepancy between Table
2 and Table 3. That comment is
addressed above under Peer Reviewer
Comments in our response to Comment
(4).
Public Comments
We received eight public comments,
three of which were from the same
individual, directly addressing the
proposed listing. Most commenters
suggested technical corrections
pertaining to the Background and
Summary of Factors Affecting the
Species sections of the proposed rule,
scientific names, species biology, and
citations. Some commenters suggested
we include additional information and
correct minor errors. We did not receive
any requests for a public hearing. The
comments are appreciated, and most
have been incorporated into the
appropriate sections of the final rule.
(6) Comment: Two commenters noted
an inaccurate statement in the proposed
listing rule that states ‘‘The life cycle of
ferns is not well known’’ (Woodmansee,
2013, pers. comm.). One of these
commenters also noted that the second
part of the same sentence mentions the
life history of Trichomanes punctatum
ssp. floridanum and then includes other
members of the genus, which is
inconsistent. One of these commenters
also noted that the next sentence in this
paragraph is incorrect and provided
edits to describe the gametophyte form
and the sporophyte form.
Our Response: We revised the
language regarding the life cycle of the
Trichomanes punctatum ssp.
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60449
floridanum in the Life History section
from not well known to not commonly
understood, as suggested by one of the
commenters. The second part of the
sentence, which includes information
on other members of the genus
Trichomanes, is unnecessary and has
been removed. We have also revised the
last sentence in that paragraph to best
describe the gametophyte and
sporophyte forms.
(7) Comment: One commenter noted
that Trichomanes punctatum ssp.
floridanum bristles do not protrude
from the sporangia, but rather one
bristle protrudes from each soral
involucre, which is the tube that also
houses the sporangia.
Response: We have corrected this
information in the Background section
of this final rule.
(8) Comment: Two commenters noted
that the four populations of
Trichomanes punctatum ssp.
floridanum within the urban preserves
of Miami-Dade County are cooperatively
managed by Miami-Dade County’s EEL
Program as well as the NAM Division of
Miami-Dade County. One of these
commenters suggested specific edits to
sections about the EEL Program and the
EEL Covenant Program. Both
commenters provided additional
information and clarification about the
impacts of Hurricane Andrew on Hattie
Bauer Hammock and the recovery of the
hammock.
Our Response: We agree that the NAM
Division of the Miami-Dade County
PROS Department and the EEL Program
are significant local partners in the
conservation of Trichomanes
punctatum ssp. floridanum. As such,
their efforts have been acknowledged in
the final rule. We have incorporated
suggested edits about the EEL Program,
the EEL Covenant Program, and Hattie
Bauer Hammock.
(9) Comment: A commenter provided
information clarifying the historical
range of the subspecies. The text in the
proposed rule reads ‘‘In Miami-Dade,
the range of this subspecies extended
from Royal Palm Hammock (now in
Everglades National Park (ENP)) at its
southern limit, northeast to Snapper
Creek Hammock, which is located in R.
Hardy Matheson Preserve.’’ The
reviewer noted that portions of
historical Snapper Creek are now
developed and are a residential
community called Smather’s Four
Fillies Farm, owned by the University of
Miami. Smather’s Four Fillies Farm is
located in the northwestern 6.5 acres of
what was historical Snapper Creek
Hammock.
Our Response: We modified the
historical range of the subspecies to
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include the additional description of the
Smather’s Four Fillies Farm residential
development within the Background
section of the final rule.
(10) Comment: One commenter noted
the proposed listing rule states, in the
Species Description section, that the
subspecies does not have roots and then
later states, in the Life History section,
that the subspecies sends out roots and
shoots. The commenter requested
clarification on this issue.
Response: The first paragraph in the
Species Description section has been
modified to state that Trichomanes
punctatum ssp. floridanum is matforming, has root-like structures, and
contains trichomes. The Life History
section has been modified to reflect that
T. punctatum ssp. floridanum is
rhizomatous (having a horizontal stem
and scale leaves, bearing aerial shoots
from its tips, and producing root-like
structures from its undersurface).
(11) Comment: One commenter noted
that the proposed listing states the
subspecies needs high temperatures and
humidity for optimum growth. The
commenter remarked that this
information is vague and temperatures
above 100 °F may be harmful to the
subspecies.
Response: We have modified our
statements regarding suitable
temperatures for Trichomanes
punctatum ssp. floridanum. In addition,
we have included new humidity and
temperature data recorded in two
Sumter County hammocks where
Trichomanes punctatum ssp.
floridanum is found.
(12) Comment: One commenter
reported that Ross Hammock continues
to exist and was not destroyed by a
hurricane in 1935. The same commenter
reported the canopy of Hattie Bauer has
also recovered after Hurricane Andrew.
Response: We have corrected these
statements in the Background section of
this final rule.
(13) Comment: One commenter noted
that we cannot definitively state that
Trichomanes punctatum ssp.
floridanum is extirpated outside of the
four known populations in Miami-Dade
County. It is possible that gametophytes
or undiscovered sporophytes exist
outside the known extant range,
particularly in the ‘‘Monkey Jungle’’
(Cox Hammock) area.
Response: We have revised this
statement in the Summary of Factors
Affecting the Species section in this
final rule.
Summary of Changes From the
Proposed Rule
Based on the information we received
from peer reviewers and public
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commenters, we made the changes
listed below. Additional minor
corrections and edits were made in the
text of the rule. We also incorporated
new temperature, humidity, and survey
information from a recent study
conducted by the IRC in Sumter County
and added information about the Clean
Water Act (CWA; 33 U.S.C. 1251 et seq.)
under Factor D. The Inadequacy of
Existing Regulatory Mechanisms.
Background Section
(1) We modified the information in
the rule regarding the relationship
between the bristles and the sporangia
of Trichomanes punctatum ssp.
floridanum and their functions.
(2) We clarified the sentence
regarding the visibility of the
sporophyte and the gametophyte of
Trichomanes punctatum ssp.
floridanum.
(3) We clarified information regarding
the historical extent of the subspecies to
include the addition of the current-day
residential community, Smather’s Four
Fillies Farm, to the description of the
Snapper Creek Hammock historical
area.
(4) We added the NAM Division of
Miami-Dade County’s PROS Department
as cooperative managers of EEL’s
preserves and clarified the difference
between the EEL Program and the EEL
Covenant Program.
(5) We clarified that Trichomanes
punctatum ssp. floridanum does not
have roots and that the subspecies is
rhizomatous.
(6) We added information regarding
challenges to propagation and the
importance of protecting extant
populations in the wild.
Summary of Factors Affecting the
Species Section
(1) We revised the information about
the impacts of the hurricane of 1935 on
the habitat at Ross Hammock and the
impacts of Hurricane Andrew on Hattie
Bauer Hammock and Trichomanes
punctatum ssp. floridanum. We also
included additional information about
the recovery and restoration of that
habitat in Hattie Bauer Hammock after
Hurricane Andrew.
(2) We added information regarding
the potential existence of Trichomanes
punctatum ssp. floridanum in MiamiDade County outside of the four known
populations, particularly in ‘‘Monkey
Jungle’’ (Cox Hammock).
Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1533),
and its implementing regulations at 50
CFR part 424, set forth the procedures
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for adding species to the Federal Lists
of Endangered and Threatened Wildlife
and Plants. Under section 4(a)(1) of the
Act, we may list a species based on one
or more 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. Listing
actions may be warranted based on any
of the above threat factors, singly or in
combination.
Information pertaining to
Trichomanes punctatum ssp.
floridanum in relation to the five factors
provided in section 4(a)(1) of the Act is
discussed below. In considering what
factors might constitute threats, we must
look beyond the mere exposure of the
species to the factor to determine
whether the species responds to the
factor in a way that causes actual
impacts to the species. If there is
exposure to a factor, but no response, or
only a positive response, that factor is
not a threat. If there is exposure and a
negative response, the factor may be a
threat, meaning that it may drive or
contribute to the risk of extinction of the
species such that the species warrants
listing as an endangered or threatened
species as those terms are defined by the
Act. This does not necessarily require
empirical proof of a threat. The
combination of exposure and some
corroborating evidence of how the
species is likely impacted could suffice.
The mere identification of factors that
could impact a species negatively is not
sufficient to compel a finding that
listing is appropriate; we require
evidence that these factors are operative
threats that act on the species to the
point that the species meets the
definition of an endangered or
threatened species under the Act.
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Habitat modification and destruction,
caused by human population growth
and development, agricultural
conversion, regional drainage, and canal
installation, have impacted the range
and abundance of Trichomanes
punctatum ssp. floridanum. Secondary
effects from hydrology and canopy
changes have resulted in changes in
humidity, temperature, and existing
water levels; loss of natural vegetation;
and habitat fragmentation. The
modification and destruction of habitat
where T.p. ssp. floridanum was once
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found has been extreme in most areas of
Miami-Dade County; while they have
been less dramatic in Sumter County,
clearing of land for agricultural
conversion and historical logging has
resulted in very few areas where the
habitat has not been modified. These
threats are discussed in detail below.
Human Population Growth,
Development, and Agricultural
Conversion
Miami-Dade County—Rockland
hammocks are considered imperiled
both locally and globally, with a limited
distribution and an FNAI ranking of G2
(imperiled globally because of rarity (6
to 20 occurrences or fewer than 3,000
individuals) or because of vulnerability
to extinction due to some natural or
manmade factor)/S2 (either very rare
and local in Florida (21–100
occurrences or fewer than 10,000
individuals) or found locally in a
restricted range or vulnerable to
extinction from other factors)) (FNAI
2010, pp. 24–26, FNAI 2013). The
tremendous development and
agricultural pressures in the rapidly
urbanizing rockland hammock areas in
south Florida have resulted in
significant reductions of this habitat
type, which is also susceptible to fire,
frost, canopy disruption, and
groundwater reduction (FNAI 2010, pp.
24–26).
Extensive land clearing for human
population growth and development in
Miami-Dade County has altered,
degraded, or destroyed hundreds of
acres of this once abundant rockland
hammock ecosystem. Rockland
hammocks once occurred across the
Miami-Rock Ridge, usually in
association with pine rocklands, or the
edges of marl prairies (areas of thin,
calcitic soil that has accumulated over
limestone bedrock) or tidal swamps
(Service 1999, p. 122). Destruction of
rocklands, including rockland
hammocks, has occurred since the
beginning of the 1900s. Historical
impacts to the environment were
addressed by Small (1938, p. 50), who
called attention to the demise of
Trichomanes punctatum ssp.
floridanum from habitat destruction,
and Phillips (1940, p. 167) who
expressed his concern for south Florida
hammocks due to the obvious and vast
amount of destruction of land in the
region. Early settlers in Florida cleared
hammocks for residential development,
farming, and range for livestock, while
industrial logging also occurred in the
region (Snyder et al. 1990, pp. 271–272).
Consistent burning of pinelands in
Miami-Dade also encroached upon
adjacent hammocks, as in the case of
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Castellow Hammock (Phillips 1940, p.
167). Habitat impacts were further
exacerbated by natural stochastic
events, such as the hurricane in 1935
that impacted Ross Hammock (Phillips
1940, p. 167).
Public conservation lands play a
significant role in the recovery of
rockland hammock habitat where future
development and habitat alteration are
less likely than on private lands.
However, these lands could be sold off
in the future and become more likely to
be developed or altered in a way that
negatively impacts the subspecies and
its habitat. Additionally, rockland
hammock may be found on private
lands; however, the fate of this existing
habitat is unknown, as it is dependent
upon actions of individual property
owners (see discussion under Factor D).
Therefore, we find that habitat loss due
to population growth, development, and
agricultural conversion poses a threat to
this subspecies in Miami-Dade County.
Sumter County—In Sumter County,
human population growth and
development has occurred, but to a
lesser degree than in Miami-Dade
County. However, Sumter County has a
long history of agriculture dating back to
the early 1860s. Generally speaking, all
land that was feasible for agriculture
was cleared at some point. In particular,
mesic hammocks where Trichomanes
punctatum ssp. floridanum occurs have
experienced disturbances from human
activities such as logging, understory
clearing, cattle grazing, and introduction
of feral hogs. These natural mesic
canopies and soils have largely been
destroyed due to their desirable
locations for living, camping, and
recreating. The global and State rank for
mesic hammock habitat (G3/S3)
signifies it is considered to have a
restricted range or be vulnerable to
extinction from other factors (FNAI
2010, p. 22).
Concerns exist regarding future
population growth and development in
those communities remaining in Sumter
County and on lands where
urbanization and agriculture have not
yet been established. According to the
Sumter County Comprehensive Plan, a
growth management paradigm has been
developed that focuses public resources
on urban areas to protect existing
undeveloped land for agricultural use
(Sumter County 2012, Data and Analysis
section). Currently, the threat with
greatest impact to T.p. ssp. floridanum
habitat in Sumter County is the
potential for agricultural and residential
clearing of mesic hammocks on small,
fragmented private parcels.
Privately owned land in the area
around Wahoo where Trichomanes
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60451
punctatum ssp. floridanum is found has
been zoned as ‘‘agricultural’’ on the
Sumter County Future Land Use Map
(Sumter County 2012, p. 42). The
County exempts single-site residential
development and agriculture from
environmental review and does not
regulate land clearing for a single
residence. Therefore, any
undocumented populations and suitable
habitat on private lands are at risk due
to land-clearing activities, agricultural
conversions, and development. For
example, one Sumter County
subpopulation observed in 1999 on
private land was extirpated due to
pasture clearing on the property for
livestock (van der Heiden 2013c, pers.
comm.). A full survey for T.p. ssp.
floridanum and associated suitable
habitat is needed in Sumter County to
determine the severity of potential
habitat loss on this subspecies
regionally, including the potential
impact from future human population
growth and development.
Due to existing agricultural and
residential clearing of mesic hammocks
and potential future clearing on private
lands, habitat loss due to human
population growth, development, and
agricultural conversion poses a threat to
T.p. ssp. floridanum in Sumter County.
Regional Drainage and Consumptive
Use
Miami-Dade County—Landscapelevel drainage has been extensive in
Miami-Dade County. In the early 1900s,
drainage initiatives were undertaken to
modify land for agriculture and
development. Impacts resulted in a
region-wide drop in the water table
(Nauman 1986, p. 182; Lodge 2005, p.
222), disturbing rockland hammocks
and their flora (Service 1999, pp. 3–
138), including Trichomanes punctatum
ssp. floridanum. Additional stress from
regional drainage for canal construction
has also contributed to the decline of
this metapopulation (Nauman 1986, p.
182; see also ‘‘Historical Range/
Distribution,’’ Miami-Dade County
section, above). As a consequence of the
pervasive drainage throughout MiamiDade County, solution holes, which
often contained standing water during
the rainy season, now hold much less,
if any, water during much of the year,
resulting in decreased ambient humidity
levels (Phillips 1940, p. 171; Nauman
1986, p. 182; Adimey 2013a, field
notes). Even though regional changes in
hydrology have not caused extirpation
of T.p. ssp. floridanum at most
locations, they may have already
induced stress by promoting
vulnerability to other stressors, such as
periodic long-term droughts, cold
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weather exposure, and other stochastic
events. Furthermore, groundwater levels
in the vicinity of T.p ssp. floridanum are
not targeted as part of the
Comprehensive Everglades Restoration
Plan (CERP) (a framework and guide to
restore, protect, and preserve the water
resources of central and southern
Florida, including the Everglades), and,
therefore, impacts from regional
drainage are not expected to be
ameliorated by CERP. Rockland
hammocks in Miami-Dade County have
been modified as a result of hydrology
changes, reducing the amount of water
available to these habitats. This is an
ongoing threat to T.p. ssp. floridanum,
as hammocks on limestone substrates
are dependent on the underlying water
table to keep humidity levels high,
especially in limestone sinkholes
(Service 1999, pp. 3–127).
Currently, the human population in
Miami-Dade County is expected to grow
to more than 4 million by 2060, an
annual increase of roughly 30,000
people (Zwick and Carr 2006, p. 20).
Although water demands will continue
to rise with population increases, the
extent of future impacts on existing
habitat and the metapopulation of
Trichomanes punctatum ssp.
floridanum in Miami-Dade County is
unknown at this time.
Sumter County—In Sumter County,
water drawdowns have historically been
minimal. Regional modeling conducted
by SWFWMD indicates less than a 0.06m (0.2-ft) current use of water in the
Upper Floridan Aquifer (Deangelis
2014a, 2014c, pers. comm.). No surface
water withdrawals are currently
occurring in Sumter County; however,
they are possible in the future.
Minimum flows and levels (MFLs),
which are water withdrawal standards
to limit water use set by the regional
water management districts, are already
established for the Withlacoochee River
portion of the Withlacoochee River
watershed in Sumter County. Although
increases in human population and
development in Sumter County may
increase water use, it is believed that
changes due to drought conditions (e.g.,
on the order of several feet) will have a
far greater impact on the hydrology
(Deangelis 2013a, pers. comm.).
Hydrology Changes
Hydrology is a key ecosystem
property that affects distribution and
viability of rare plants (Gann et al. 2009,
p. 6). Hydrology changes have
extensively modified and, in some
cases, destroyed habitat in south
Florida. As a result of human
population growth, development,
agricultural conversion, and regional
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drainage, the hydrology of Trichomanes
punctatum ssp. floridanum habitat has
changed drastically and has contributed
to the alteration in ambient humidity
and temperature.
For a hygrophilous (living or growing
in damp places) subspecies thought to
be restricted to a consistently humid
¨
microhabitat (Kromer and Kessler 2006,
p. 57), high humidity is a critical factor
to its survival, so any habitat
modification or destruction that changes
ambient humidity levels poses a threat
to this subspecies (Nauman 1986, p.
182). As noted above, drainage efforts
implemented in south Florida have
significantly reduced historical water
table levels, altering ambient humidity
in the area. It is speculated that this
subspecies may be living in discrete
areas where humidity may be at the
threshold for T.p. ssp. floridanum to
survive. Minor drops in ambient
humidity may limit reproduction and
can negatively impact overall health of
existing metapopulations, as well as
inhibit the growth of new plants,
impacting long-term viability (van der
Heiden, 2013c, pers. comm.; Possley
2013e, pers. comm.). Van der Heiden
and Johnson (2014, p. 9) recently
observed this in Sumter County, where
small drops in ambient temperature and
humidity resulted in observed declines
in the health of some clusters of T.p.
ssp. floridanum within the local
population.
Canopy Changes
Canopy also is an important habitat
feature for Trichomanes punctatum ssp.
floridanum, and, in most cases, is the
primary factor controlling surrounding
temperature and humidity levels that
are critical to the survival of this
subspecies. The proper amount of high
shade and low light is critical for the
persistence of this subspecies. These
features help to maintain humidity and
prevent desiccation from excessive light
exposure (van der Heiden 2013c, pers.
comm.; Possley 2013e, pers. comm.;
Adimey 2013a–b, field notes).
Currently, in both metapopulations,
dense canopy cover is a necessity;
however, the amount of canopy density
needed to ensure survival is not yet
known. Changes to existing canopies
can result from land clearing and
conversion, natural stochastic events,
competition with nonnative species,
and nonnative species control (see
discussion under Factor E).
Historically, as land was developed,
natural features of the landscape
changed, directly eliminating
Trichomanes punctatum ssp.
floridanum and also eliminating
surrounding vegetation and habitat
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features essential to this subspecies.
Field observations in Miami-Dade
County have found clusters of T.p. ssp.
floridanum desiccated when the
immediate canopy above the ferns was
destroyed or substantially reduced,
allowing high amounts of light into the
understory (Possley 2013g, pers.
comm.); however, over the course of
many months, these clusters eventually
recovered.
The loss of canopy can result in plant
desiccation via increased sun and wind
exposure, increased ambient
temperatures, changes in ambient
humidity, and the proliferation of exotic
species (see Factor E discussion, below).
Destruction or changes in canopy of any
existing populations could result in
elimination of an entire population.
Therefore, we find the loss of canopy
through habitat loss and modification to
be a threat to T.p. ssp. floridanum.
Habitat Fragmentation
Habitat fragmentation limits dispersal
and population size, and promotes
vulnerability among existing
populations. In Miami-Dade County,
most remaining Trichomanes
punctatum ssp. floridanum habitat (i.e.,
Fuchs, Meissner, Castellow, Hattie
Bauer hammocks) is surrounded by
housing development and agricultural
land, resulting in scattered and small
natural areas. Regional drainage and
hydrology changes may also have
contributed to the fragmented habitat in
Miami-Dade County. In Sumter County,
the impacts of habitat fragmentation are
not as severe, as conservation lands are
on large, adjacent tracts. Future
development in Sumter County could
result in an increase in fragmented
habitat and pose a threat for this
northern metapopulation (van der
Heiden 2013c, pers. comm.). However,
data regarding the impacts and
subsequent consequences from habitat
fragmentation are incomplete for both
metapopulations of Trichomanes
punctatum ssp. floridanum. Information
and understanding of dispersal
mechanisms for this subspecies are also
currently lacking. The best available
data for other plant species regarding
the impacts of habitat fragmentation
suggest that habitat fragmentation is
likely a stressor impacting this
subspecies but does not indicate that it
rises to the level of a threat.
Conservation Efforts To Reduce Habitat
Destruction, Modification, or
Curtailment of Its Range
Conservation efforts to reduce habitat
destruction are generally focused on the
conservation of land on which both
metapopulations occur. All known
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extant populations occur on State- or
County-owned land that is currently
protected from future development. In
Miami-Dade County, extant occurrences
of Trichomanes punctatum ssp.
floridanum have been protected through
acquisition within the County’s EEL
Program.
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Fee Title Properties
In 1990, Miami-Dade County voters
approved a 2-year property tax to fund
the acquisition, protection, and
maintenance of natural areas by the EEL
Program. The EEL (acquisition) Program
purchases and manages natural lands
for preservation. Land uses deemed
incompatible with the protection of the
natural resources are prohibited by
current regulations; however, the
County Commission ultimately controls
what may happen with any County
property, and land use changes may
occur over time (Gil 2013b, pers.
comm.). To date, the Miami-Dade
County EEL Program has acquired a
total of approximately 95 ha (236 ac) of
tropical hardwood and rockland
hammocks (Gil 2013b, pers. comm.).
The EEL Program also manages
approximately 639 ha (1,578 ac) of
tropical hardwood and rockland
hammocks known as EEL Preserves and
owned by the Miami-Dade County
PROS Department, including some of
the largest remaining areas of tropical
hardwood and rockland hammocks (e.g.,
Matheson Hammock Park, Castellow
Hammock Park, and Deering Estate Park
and Preserves). The EEL Program may
acquire lands that were once under an
EEL Covenant (see description below).
However, the existence of an EEL
Covenant is not a requirement or
precursor for acquisition of lands under
the EEL Program.
EEL Covenant Program
In 1979, Miami-Dade County
established the EEL Covenant Program
to reduce taxes for private landowners
who own natural forest communities
(NFC), such as pine rocklands and
rockland hammocks. Under the EEL
Covenant Program, landowners agree
not to develop their property and to
manage it for a period of 10 years, with
the option to renew for additional 10year periods (Service 1999, pp. 3–177).
The EEL Covenant Program currently
protects approximately 119 rockland
hammock properties, comprising
approximately 315.65 ha (780 ac) of
habitat (Joyner 2013b, pers. comm.).
Although these temporary
conservation easements provide
valuable protection for their duration,
they are not considered under Factor D,
below, because they are voluntary
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agreements and not regulatory in nature.
Miami-Dade County currently has
approximately 21 rockland hammock
properties enrolled in this program,
preserving 20.64 ha (51 ac) of rockland
hammock habitat (Joyner 2013b, pers.
comm.). The vast majority of these
properties are small, and many are in
need of habitat management, such as
removal of nonnative, invasive plants.
Although the EEL Covenant Program
has the potential to provide valuable
habitat for unknown or future
populations of Trichomanes punctatum
ssp. floridanum, the actual contribution
of these designated conservation lands
is largely determined by whether
individual landowners follow
prescribed EEL management plans and
NFC regulations (see ‘‘Local’’ under
Factor D below).
The County- and State-owned land
areas that are protected by the EEL
Program are critical to providing habitat
for Trichomanes punctatum ssp.
floridanum, as well as other native flora
in Florida. Conservation efforts to
prevent the future extirpation of T. p.
ssp. floridanum and other fern species
in Miami’s EEL Preserves have been
under way for many years. In MiamiDade County, conservation lands are
and have been monitored by Fairchild
and IRC, in coordination with the EEL
Program and the NAM Division of
Miami-Dade County’s PROS
Department, to assess habitat status and
determine any changes that may pose a
threat to or alter the abundance of T. p.
ssp. floridanum (Possley 2013k, pers.
comm.; van der Heiden 2013f–h, pers.
comm.). Impacts to habitat (e.g., canopy)
via nonnative species and natural
stochastic events are monitored and
actively managed in areas where the
taxon is known to occur. These
programs are long term and ongoing in
Miami-Dade County; however, programs
are limited by the availability of annual
funding.
Other Efforts
To date, only one reintroduction of
filmy ferns (no specific species was
indicated) was attempted by F.C.
Craighead in the early 1960s, in several
hammocks within ENP within the Long
Pine Key area. These efforts were
unsuccessful, but no explanation was
provided as to why they were
unsuccessful (Gann 2013). Within-range
reintroductions into unoccupied habitat
have historically resulted in low success
rates for plants (Maschinski et al. 2011,
p. 159). Future reintroduction efforts
will likely be attempted by MSBG from
Trichomanes punctatum ssp.
floridanum plants grown in-vitro from
CREW.
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60453
In Sumter County, monitoring and
management in Withlacoochee State
Forest is provided through the Florida
Forest Service (Werner 2013e, pers.
comm.). Habitat is assessed annually for
canopy changes that may alter ambient
humidity levels and for impacts from
nonnative plant species and feral pigs.
Additionally, surveys on SWFWMD
property are conducted periodically to
assess habitat and search for rare plant
species in the area (Deangelis 2013b,
pers. comm.).
Summary of Factor A
Past human actions have destroyed,
modified, and curtailed the range and
habitat available for Trichomanes
punctatum ssp. floridanum. Human
population growth and development,
agricultural conversion, and regional
drainage have modified, or in most
cases, destroyed, habitat where T. p.
ssp. floridanum once occurred, thereby
limiting the subspecies’ current range
and abundance in Florida.
In Miami-Dade County, habitat
modification and destruction have
severely impacted rockland hammocks
that were once abundant. The
Trichomanes punctatum ssp.
floridanum metapopulation in MiamiDade County is currently composed of
four known populations, all on Countymanaged conservation lands.
Historically, T. p. ssp. floridanum was
found in an additional nine hammocks
in Miami-Dade County. Most of these
populations have been extirpated, and
the historical range of the southern
metapopulation has been reduced by
nearly 80 percent. However, the
subspecies was observed in ‘‘Monkey
Jungle’’ (historically referred to as Cox
Hammock) in 1989, and no thorough
surveys have been conducted there
since then. Upon recent visitation to the
site (Adimey 2013a, field notes), the
habitat features appeared to be similar
to other hammocks where T. p. ssp.
floridanum is currently known to occur
(large solution holes, high humidity,
dense canopy, standing water). Thus,
much of the habitat has been destroyed,
and while those fragments suitable for
the plant remain protected in MiamiDade County, habitat loss and
modification from future development
or conversion on private and
conservation lands in Miami-Dade
County poses a threat. In addition, the
areas where T. p. ssp. floridanum
currently exists are still vulnerable to
activities in the surrounding areas,
including agricultural clearing and
hydrologic alterations.
The Sumter County metapopulation
of Trichomanes punctatum ssp.
floridanum is composed of two known
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populations, both on State-owned land
in the Jumper Creek Tract of the WSF.
In central Florida, the subspecies was
historically found in as many as seven
additional locations. All of these
historical populations have since been
extirpated, primarily due to land
conversion and clearing (including for
cattle grazing) and the impacts of local
and regional drainage. Land clearing
and hydrological alterations on private
lands adjacent to the Jumper Creek Tract
continue to be threats to T. p. ssp.
floridanum populations and habitat.
The destruction and modification of
habitat have resulted in changes in
canopy, humidity, hydrology, and
fragmentation that have contributed to
the declines of this taxon. High
humidity and dense canopy cover are
critical for Trichomanes punctatum ssp.
floridanum’s survival. Therefore, any
habitat modification or destruction that
changes ambient humidity levels or
canopy cover poses a threat to this
subspecies. Data regarding the impacts
of habitat fragmentation are incomplete
for both metapopulations of T. p. ssp.
floridanum because information on
dispersal mechanisms of this subspecies
is currently lacking. Habitat
fragmentation is likely a stressor
impacting this subspecies, but the best
available data do not indicate that it
rises to the level of a threat.
Conservation efforts are currently
providing some benefits to this
subspecies but are not sufficient to
ameliorate the habitat threats. Therefore,
based on the best information available,
we have determined that the threats to
Trichomanes punctatum ssp.
floridanum from habitat destruction,
modification, or curtailment are
occurring throughout the entire range of
the species and are expected to continue
into the future.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Under this factor, we examine
whether threats to the subspecies
discussed under the other factors are
continuing due to an inadequacy of an
existing regulatory mechanism. Section
4(b)(1)(A) of the Act requires the Service
to take into account ‘‘those efforts, if
any, being made by any State or foreign
nation, or any political subdivision of a
State or foreign nation, to protect such
species . . . .’’ In relation to Factor D
under the Act, we interpret this
language to require the Service to
consider relevant Federal, State, and
tribal laws, regulations, and other such
mechanisms that may minimize any of
the threats we describe in threat
analyses under the other four factors, or
otherwise enhance conservation of the
species. We give strongest weight to
statutes and their implementing
regulations and to management
direction that stems from those laws and
regulations. An example would be State
governmental actions enforced under a
State statute or constitution or Federal
action under statute.
Having evaluated the impact of the
threats as mitigated by any such
conservation efforts, we analyze under
Factor D the extent to which existing
regulatory mechanisms are inadequate
to address the specific threats to the
species. Regulatory mechanisms, if they
exist, may reduce or eliminate the
impacts from one or more identified
threats. In this section, we review
existing Federal, State, and local
regulatory mechanisms designed to
address threats to Trichomanes
punctatum ssp. floridanum to determine
whether they effectively reduce or
remove threats to the subspecies.
Federal
The only known extant populations of
Trichomanes punctatum ssp.
Factor B. Overutilization for
floridanum occur on State- or CountyCommercial, Recreational, Scientific, or owned properties, and development of
Educational Purposes
most of these areas is not likely to
require a Federal permit or other
The best available data do not
authorization.
indicate that overutilization for
Section 404 of the Clean Water Act
commercial, recreational, scientific, or
(CWA; 33 U.S.C. 1251 et seq.)
educational purposes is occurring and,
establishes a Federal program for
therefore, we find that overutilization is regulating the discharge of dredged or
not a threat to Trichomanes punctatum
fill material into waters of the United
ssp. floridanum.
States, including wetlands.
Additionally, section 401 of the CWA
Factor C. Disease or Predation
forbids Federal agencies from issuing a
No diseases or incidences of
permit or license for activities that may
predation have been reported for
result in a discharge to waters of the
Trichomanes punctatum ssp.
United States until the State or Tribe
floridanum. Therefore, the best available where the discharge would originate has
data do not indicate that disease or
granted or waived certification. The
State of Florida maintains regulatory
predation is a threat to the subspecies.
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programs providing a framework for
issuance of section 401 certifications
related to applications for section 404
permits. This legislation does not
prohibit the discharge of these materials
into wetlands; rather, it provides a
regulatory framework that requires
permits prior to such action being taken.
The U.S. Army Corps of Engineers
(Corps) reviews individual permits for
potentially significant impacts;
however, most discharges are
considered to have minimal impacts
and may be covered by a general permit
that does not require individual review.
On June 29, 2015, the Environmental
Protection Agency and Corps published
a final rule (80 FR 37054), effective
August 28, 2015, that revises the
definition of ‘‘waters of the United
States.’’ Specific guidance on
implementation of this revised
definition is currently lacking, but it
appears that the revised definition is
likely to include hydric hammocks in
areas where Trichomanes punctatum
ssp. floridanum occurs in Sumter
County among waters of the United
States. However, as noted above, section
404 of the CWA does not necessarily
prevent degradation to such habitats
from the discharge of dredge or fill
material. It simply provides a regulatory
program for permitting activities that
would result in such a discharge.
Further, discharges associated with
normal farming, ranching, and forestry
activities, such as plowing, cultivating,
minor drainage, and harvesting for the
production of food, fiber, and forest
products are exempt from the
requirement to obtain a permit.
State
FNAI considers the State status of
Trichomanes punctatum ssp.
floridanum to be S1, ‘‘critically
imperiled in Florida because of extreme
rarity (five or fewer occurrences or less
than 1,000 individuals) or because of
extreme vulnerability to extinction due
to some natural or man-made factor’’
(FNAI, 2013; Element Tracking
Summary). The IRC considers its status
as ‘‘critically imperiled’’ (Gann et al.
2002, pp. 552–554).
The Florida Department of
Agriculture and Consumer Services has
listed Trichomanes punctatum ssp.
floridanum on the Regulated Plant
Index (Index) as endangered under
Chapter 5B–40, Florida Administrative
Code (State of Florida 2013, Florida
Statutes). This listing provides little or
no habitat protection beyond the State’s
Development of Regional Impact
process, which discloses impacts from
projects, but provides no regulatory
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protection for State-listed plants on
private lands.
Florida Statutes chapter 581.185,
sections (3)(a) and (b), prohibit any
person from willfully destroying or
harvesting any species listed as
endangered or threatened on the Index,
or growing such a plant on the private
land of another, or on any public land,
without first obtaining the written
permission of the landowner and a
permit from the Florida Department of
Plant Industry. The statute further
provides that any person willfully
destroying or harvesting; transporting,
carrying, or conveying on any public
road or highway; or selling or offering
for sale any plant listed in the Index as
endangered must have a permit from the
State at all times when engaged in any
such activities. Further, section (10) of
the statute provides for consultation
similar to section 7 of the Act for listed
species, by requiring the Department of
Transportation to notify the FDACS and
the Endangered Plant Advisory Council
of planned highway construction at the
time bids are first advertised, to
facilitate evaluation of the project for
listed plant populations, and to
‘‘provide for the appropriate disposal of
such plants’’ (i.e., transplanting).
However, this statute provides no
substantive protection of habitat or
protection of potentially suitable habitat
at this time. Sections (8)(a) and (b) of the
statute waive State regulation for certain
classes of activities for all species on the
Index, including the clearing or removal
of regulated plants for agricultural,
forestry, mining, construction
(residential, commercial, or
infrastructure), and fire-control
activities by a private landowner or his
or her agent.
The Florida Forest Service (FFS) is
the lead managing agency for State
forests, as outlined in the Management
Lease from the landowner (Board of
Trustees of the Internal Improvement
Trust Fund of the State of Florida) with
guidance provided in chapters 253, 259,
and 589 of the Florida Statutes (State of
Florida, 2013 Florida Statutes,
Preservation of Native Flora and Fauna).
FFS is responsible for the management
and supervision of the multiple-use
guidelines of Withlacoochee State
Forest. For research on State forest
lands, prior approval is required.
Research deemed legitimate will be
issued a State Forest Use Permit
(FDACS–11228) or letter of
authorization (The Florida Forest
Service 2013, State Forest Handbook).
Although the MFLs established by the
South Florida Water Management
District (SFWMD) in southeast Florida
(a separate entity from the SWFWMD
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described earlier) are not directly
applicable in the area of Miami Rock
Ridge where Trichomanes punctatum
ssp. floridanum occurs, they do
indirectly limit ground water
withdrawals in other areas of south
Florida, including other areas of the
Miami Rock Ridge. Unfortunately, MFL
thresholds in place that establish water
withdrawal standards are set so low that
protection measures are rarely triggered.
These low water level standards may be
further exacerbated during times of
drought, resulting in even greater
impacts to the water table and the
overall regional hydrology.
Furthermore, MFL standards also do not
apply to wells on private property or for
consumptive use. The lowering of
ground water and associated changes in
local ambient humidity have already
occurred throughout south Florida and
have likely contributed to the decline of
T. p. ssp. floridanum and possibly
limited distribution and resilience (i.e.,
ability to withstand stochastic (random)
events and recover from disturbances) of
the subspecies (Grossenbacher 2013,
pers. comm.). Plants are likely to be
further stressed by the continued
lowering of ground water if additional
large wells are created on private
property for such activities as
agriculture or during extended periods
of drought because these types of
circumstances are not regulated by the
water withdrawal standards established
by the SFWMD. In general, this
regulatory mechanism has not been
sufficient to reduce or remove the threat
to T. p. ssp. floridanum posed by
changes in hydrology discussed under
Factor A by ensuring that current water
levels will persist into the future.
Sumter County MFLs identified and
adopted by the SWFWMD protect the
Withlacoochee River and the Tsala
Apopka lake chain, which connects to
the Withlacoochee in the vicinity of
Jumper Creek Tract where Trichomanes
punctatum ssp. floridanum occurs.
Maintaining designated MFLs will have
a direct bearing on the design of future
water supply development projects, of
which there are several already
proposed in Sumter County (Deangelis
2014c, pers. comm.). However, it is
uncertain how these future projects
would impact extant occurrences of T.
p. ssp. floridanum or suitable habitat for
the subspecies.
Local
In 1984, section 24–49 of the Code of
Miami-Dade County established
regulation of County-designated NFCs.
These regulations were placed on
specific properties throughout the
County by an act of the Board of County
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Commissioners in an effort to protect
environmentally sensitive forest lands.
The Miami-Dade County Department of
Regulatory and Economic Resources
(RER) has regulatory authority over
these County-designated NFCs and is
charged with enforcing regulations that
provide partial protection of remaining
upland forested areas designated as NFC
on the Miami Rock Ridge. NFC
regulations are designed to prevent
clearing or destruction of native
vegetation within preserved areas.
Miami-Dade County Code typically
allows up to 10 percent of a rockland
hammock designated as NFC to be
developed for properties greater than 5
acres and requires that the remaining 90
percent be placed under a perpetual
covenant for preservation purposes
(Joyner 2013a, 2014, pers. comm; Lima
2014, pers. comm.). However, for
properties less than 5 acres, up to onehalf an acre can be cleared if the request
is deemed a reasonable use of property;
this allowance often can be greater than
10 percent of the property (Lima, 2014,
pers. comm.). NFC landowners are also
required to obtain an NFC permit for
any work, including removal of
nonnatives, within the boundaries of the
NFC on their property. When
discovered, unpermitted work is
pursued by RER through appropriate
enforcement action, and restoration is
sought when possible. The NFC
program is responsible for ensuring that
NFC permits are issued in accordance
with the limitations and requirements of
the county code and that appropriate
NFC preserves are established and
maintained in conjunction with the
issuance of an NFC permit when
development occurs.
Although the NFC program is
designed to protect rare and important
upland (non-wetlands) habitats in south
Florida, it is a regulatory strategy with
limitations. For example, in certain
circumstances where landowners can
demonstrate that limiting development
to 10 percent does not allow for
‘‘reasonable use’’ of the property,
additional development may be
approved. Furthermore, Miami-Dade
County Code provides for up to 100
percent of the NFC to be developed in
limited circumstances for parcels less
than 2.02 ha (5 ac) in size and requires
coordination with the landowners only
if they plan to develop property or
perform work within the NFC
designated area. As such, many of the
existing private forested NFC parcels
remain fragmented, without
management obligations or preserve
designation, as development has not
been proposed at a level that would
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trigger the NFC regulatory requirements.
Often, nonnative vegetation over time
begins to dominate and degrade the
undeveloped and unmanaged NFC
landscape until it no longer meets the
legal threshold of an NFC, which
requires the land to be dominated by
native vegetation. When development of
such degraded NFCs is proposed,
Miami-Dade County Code requires
delisting of the degraded areas as part of
the development process. Property
previously designated as NFC is
removed from the list even before
development is initiated because of the
abundance of nonnative species, making
it no longer considered to be
jurisdictional or subject to the NFC
protection requirements of the MiamiDade County Code (Grossenbacher 2013,
pers. comm.).
Although Trichomanes punctatum
ssp. floridanum is currently afforded
some protection from outright
destruction on public conservation land,
changes in the surrounding landscape
that affect the subspecies are not
regulated. For example, the private
property known as ‘‘Monkey Jungle’’
(historically referred to as Cox
Hammock) is a public attraction and is
home to a considerable number of
primate species. Upon recent visitation
to this site (Adimey 2013a, field notes),
the habitat features appeared to be
similar to other hammocks where T. p.
ssp. floridanum currently is known to
live (i.e., large solution holes, high
humidity, dense canopy, standing
water). Although much of the hammock
has been altered to accommodate
captive animals and visitors, a
significant portion of the hammock still
remains untouched and overgrown with
extensive nonnative, invasive plant
species. ‘‘Monkey Jungle’’ receives
limited protection under the MiamiDade County Environmental Protection
Ordinance as an NFC, where only
portions of NFCs can be cleared once a
permit is obtained from the County.
Additionally, Miami-Dade County has
oversight of any work or research
completed within the local preserve
areas; permits are required for any
outside work or research on Countyowned lands in order to further protect
the habitat from potential direct or
indirect impacts (Gil 2013a, pers.
comm.).
Under section 13–644(a)(1) of the
Sumter County code, ‘‘[m]ajor
developments shall identify and protect
habitats of protected wildlife and
vegetation species,’’ and in section 13–
644(a)(1)2.b.2, ‘‘[n]o permit will be
issued for development which results in
unmitigated destruction of specimens of
endangered, threatened or rare species.’’
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Therefore, the County code prevents
unmitigated destruction of endangered,
threatened, or rare species only when
associated with ‘‘major developments.’’
Current zoning in the Wahoo area limits
development to one unit per 4 ha (10
ac); therefore, ‘‘major developments’’ do
not seem to be likely in that area. In
general, existing county ordinances do
not prevent the conversion of habitat to
agricultural use or building on sites
with endangered, threatened, or rare
plant species. Without complete survey
information for Sumter County, it is
difficult to assess the extent to which
unknown occurrences and suitable
habitat on private lands are at risk.
Agriculture and development are
ongoing and promoted in this County,
and no regulatory mechanisms exist that
protect T. p. ssp. floridanum and its
habitat on private lands.
Summary of Factor D
Currently, Trichomanes punctatum
ssp. floridanum is only known to occur
on State and County lands; however,
there are no regulatory mechanisms in
place that provide substantive
protection of habitat or protection of
potentially suitable habitat at this time.
In addition, subsections of applicable
statutes waive State regulation for
private landowners or their agents,
allowing certain activities to clear or
remove species on the Index. Little, if
any, protection is afforded to T. p. ssp.
floridanum by the established MFLs in
south Florida, as they are set very low,
are rarely triggered, and are not
applicable in the portion of the Miami
Rock Ridge where the subspecies
currently lives. Established MFLs in
Sumter County can positively impact
areas where T. p. ssp. floridanum
occurs, provided that these designated
MFLs are maintained when future water
supply development projects are
undertaken. The NFC program in Miami
is designed to protect rare and
important upland (non-wetland)
habitats in south Florida. However, this
regulatory strategy has several
limitations that can negatively affect T.
p. ssp. floridanum. Sumter County code
prevents unmitigated destruction of
endangered, threatened, or rare species
only when associated with ‘‘major
developments’’ and does not prevent
conversion of habitat to agricultural use
or building on private property.
Although all known extant
populations of Trichomanes punctatum
ssp. floridanum are afforded some level
of protection because they are on public
conservation lands, existing regulatory
mechanisms have not led to a reduction
or removal of threats posed to the
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subspecies by a wide array of sources
(see discussions under Factors A and E).
Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence
Other natural or manmade factors
affect Trichomanes punctatum ssp.
floridanum to varying degrees. Specific
threats include the spread of nonnative,
invasive species; potentially
incompatible management practices
(e.g., inadvertent spraying of T. p. ssp.
floridanum while controlling for
nonnatives); direct impacts to plants
from recreation and other human
activities; small population size and
isolation; climate change; and the
related risks from environmental
stochasticity (extreme weather). Each of
these threats and its specific effect on T.
p. ssp. floridanum is discussed in detail
below.
Nonnative Species
Nonnative species can stress, alter, or
even destroy native species and their
habitats. The threat of nonnative plant
species is ongoing due to their: (1)
Number and extent, (2) ability to outcompete native species, (3) abundant
seed sources, and (4) extensive
disturbance within habitats. Further
challenges exist due to limitation of
resources to combat this threat, as well
as the difficulty in managing fragmented
hammocks bordered by urban
development, which often can serve as
seed sources for nonnative species
(Bradley and Gann 1999, p. 13).
Nonnative, invasive plants compete
with native plants for space, light,
water, and nutrients, and they limit
growth and abundance of natural
vegetation and can make habitat
conditions unsuitable for native plants.
In south Florida, at least 162
nonnative plant species are known to
invade rockland hammocks. Impacts are
particularly severe on the Miami Rock
Ridge (Service 1999, pp. 3–135).
Nonnative plant species have
significantly affected rockland
hammock and mesic hammock habitats
where Trichomanes punctatum ssp.
floridanum occurs and are considered
one of the threats with greatest impact
to the subspecies (Snyder et al. 1990, p.
273; Gann et al. 2002, pp. 552–554;
FNAI 2010, pp. 22, 26). Nonnative
plants outcompete and displace T. p.
ssp. floridanum in solution holes, and
may form dense strata (layers) in the
hammock, where it is possible that the
fern may be blanketed and smothered
(Possley 2014c, pers. comm.). It has also
been suggested that the insular nature of
south Florida, as well as the hammocks
themselves, predispose this habitat to
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invasion by nonnative plants (e.g., the
proximity of seed sources, which
increases the volume of nonnatives and
accelerates the time it takes for the
arrival and establishment of nonnatives)
(Horvitz et al. 1998, p. 961).
In many Miami-Dade County parks,
nonnative plant species comprise 50
percent of the flora in hammock
fragments (Service 1999, pp. 3–135).
Horvitz (et al. 1998, p. 968) suggests the
displacement of native species by
nonnative species in conservation and
preserve areas is a complex problem
with serious impacts to biodiversity
conservation. Problematic nonnative
invasive plants in Miami-Dade County
associated with Trichomanes
punctatum ssp. floridanum include
Schinus terebinthifolia (Brazilian
pepper), Bischofia javanica (bishop
wood), Syngonium podophyllum
(American evergreen), Jasminum
fluminense (Brazilian jasmine), Rubus
niveus (mysore raspberry), Thelypteris
opulenta (jeweled maiden fern),
Nephrolepis multiflora (Asian
swordfern), Schefflera actinophylla
(octopus tree), Jasminum dichotomum
(Gold Coast jasmine), Epipremnum
pinnatum (centipede tongavine), and
Nephrolepis cordifolia (narrow
swordfern) (Possley 2013g–h, pers.
comm.).
In Sumter County, the most
problematic nonnative invasive species
occurring in Trichomanes punctatum
ssp. floridanum habitat are Tradescantia
fluminensis (small leaf spiderwort) and
Paederia foetida (skunkvine) (Werner
2013d, pers. comm.). Furthermore,
Citrus aurantium (bitter orange) is found
in this locale and is considered
problematic due to its tendency to
attract feral hogs, another nonnative
species associated with extensive
habitat destruction (see below).
Agricultural fields in proximity to the
Sumter metapopulation are a nonnative
seed source, increasing potential
encroachment of nonnative plants to the
area (Werner 2013b–c, pers. comm.).
In some instances, management of
nonnative vegetation may also be
detrimental, in that nonnative species
may actually provide the necessary
canopy to limit sunlight exposure and
control humidity, so that removing the
nonnative species exposes the fern. In
Castellow Hammock, the majority of the
shade near two of the large solution
holes containing Trichomanes
punctatum ssp. floridanum is provided
by giant Schinus terebinthifolia trees;
eliminating these trees could likely
result in detrimental effects to T. p. ssp.
floridanum residing in the underlying
solution holes. In hammocks such as
Castellow, desiccation from excessive
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sun exposure due to the removal of S.
terebinthifolia canopy has already
occurred. In this case, the
subpopulation of T. p. ssp. floridanum
below the S. terebinthifolia tree turned
brown; however, T. p. ssp. floridanum
could eventually revitalize if sufficient
canopy is reestablished to limit sunlight
exposure (Possley 2013d, pers. comm.).
Additionally, nonnative plant control
may also become a threat when T. p.
ssp. floridanum is inadvertently sprayed
while authorities conduct local
nonnative removal efforts (Possley
2013d, pers. comm.).
Nonnative plant species are also a
concern on private lands, where often
these species are not controlled due to
associated costs, lack of interest, or lack
of knowledge of detrimental impacts to
the ecosystem. Overall, active
management is necessary to control for
nonnative species and to protect unique
and rare habitat where T.p. ssp.
floridanum occurs (Snyder et al. 1990,
p. 273). Treatment of nonnative plant
species should consider canopy and
humidity needs of T.p. ssp. floridanum.
Nonnative feral hogs living in the
Withlacoochee State Forest are also
considered a threat to this plant.
Surveys in Sumter County have
revealed evidence of hogs lying against
or rubbing their bodies against large
rocks, removing existing vegetation in
the process. Recently, van der Heiden
and Johnson (2014, p. 11) found one
small rock where Trichomanes
punctatum ssp. floridanum had been
scraped off when a hog rubbed itself on
the rock after wallowing in the mud.
Furthermore, rooting from hogs can
destroy existing habitat by displacing
smaller rocks where T.p. ssp.
floridanum is found to grow and
potentially damaging or eliminating a
cluster (Werner 2013d, pers. comm.). In
Withlacoochee State Forest, damaged
areas from feral hogs are also more
susceptible to invasion from nonnative
plant species, such as Urena lobata
(Caesarweed) and Tradescantia
fluminensis (small-leaf spiderwort)
(Werner 2013a, pers. comm.). If feral
hogs continue to forage in areas where
T.p. ssp. floridanum lives, it is possible
that entire clusters inhabiting one rock/
boulder could be eliminated.
In recent years, scientists in south
Florida have noticed an increase in
sightings of the nonnative genus
Zachrysia (Cuban tree snails). Although
snail grazing has not been observed on
Trichomanes punctatum ssp.
floridanum, it has been documented on
other rare ferns living in the same
habitat and could possibly become a
threat in the future, either by this snail
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or another introduced species (Possley
2013b, c, pers. comm.).
Climate Change
Climatic changes, including sea level
rise (SLR), are occurring in the State of
Florida and are impacting associated
plants, animals, and habitats. The term
‘‘climate,’’ as defined by the
Intergovernmental Panel on Climate
Change (IPCC), refers to the mean and
variability of different types of weather
conditions over time, with 30 years
being a typical period for such
measurements, although shorter or
longer periods also may be used (IPCC
2013, p. 1450). The term ‘‘climate
change,’’ thus, refers to a change in the
mean or variability of one or more
measures of climate (e.g., temperature or
precipitation) that persists for an
extended period, typically decades or
longer, whether the change is due to
natural variability, human activity, or
both (IPCC 2013, p. 1450). A recent
compilation of climate change and its
effects is available from reports of the
IPCC (IPCC 2013, entire).
Various changes in climate may have
direct or indirect effects on species.
These effects may be positive, neutral,
or negative, and they may change over
time, depending on the species and
other relevant considerations, such as
interactions of climate with other
variables (e.g., habitat fragmentation)
(IPCC 2007, pp. 8–14, 18–19). Projected
changes in climate and related impacts
can vary substantially across and within
different regions of the world (e.g., IPCC
2007, p. 8–12). Therefore, we use
‘‘downscaled’’ projections when they
are available and have been developed
through appropriate scientific
procedures (see Glick et al. 2011, pp.
58–61, for a discussion of downscaling).
As to Trichomanes punctatum ssp.
floridanum, downscaled projections
suggest that SLR is the largest climatedriven challenge to low-lying coastal
areas in the subtropical ecoregion of
southern Florida (U.S. Climate Change
Science Program (USCCSP) 2008, pp. 5–
31, 5–32). All Miami-Dade County
populations of T.p. ssp. floridanum
occur at elevations 2.83–4.14 m (9.29–
13.57 ft) above sea level, making the
subspecies highly susceptible to
increased storm surges and related
impacts associated with SLR, whereas
the Sumter County populations are at
approximately 10.40 m (34.12 ft) above
sea level and significantly farther from
the coast.
The long-term record at Key West
shows that sea level rose on average
0.229 cm (0.090 in) annually between
1913 and 2013 (National Oceanographic
and Atmospheric Administration
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(NOAA) 2013, p. 1). This equates to
approximately 22.9 cm (9.02 in) over the
last 100 years. IPCC (2008, p. 28)
emphasized it is very likely that the
average rate of SLR during the 21st
century will exceed the historical rate.
The IPCC Special Report on Emission
Scenarios (2000, entire) presented a
range of scenarios based on the
computed amount of change in the
climate system due to various potential
amounts of anthropogenic greenhouse
gases and aerosols in 2100. Each
scenario describes a future world with
varying levels of atmospheric pollution
leading to corresponding levels of global
warming and corresponding levels of
SLR. The IPCC Synthesis Report (2007,
entire) provided an integrated view of
climate change and presented updated
projections of future climate change and
related impacts under different
scenarios.
Subsequent to the 2007 IPCC Report,
the scientific community has continued
to model SLR. Recent peer-reviewed
publications indicate a movement
toward increased acceleration of SLR.
Observed SLR rates are already trending
along the higher end of the 2007 IPCC
estimates, and it is now widely held that
SLR will exceed the levels projected by
the IPCC (Rahmstorf et al. 2012, p. 1;
Grinsted et al. 2010, p. 470). Taken
together, these studies support the use
of higher end estimates now prevalent
in the scientific literature. Recent
studies have estimated global mean SLR
of 1.0–2.0 m (3.3–6.6 ft) by 2100 as
follows: 0.75–1.90 m (2.50–6.20 ft;
Vermeer and Rahmstorf 2009, p. 21530),
0.8–2.0 m (2.6–6.6 ft; Pfeffer et al. 2008,
p. 1342), 0.9–1.3 m (3.0–4.3 ft; Grinsted
et al. 2010, pp. 469–470), 0.6–1.6 m
(2.0–5.2 ft; Jevrejeva et al. 2010, p. 4),
and 0.5–1.4 m (1.6–4.6 ft; National
Research Council 2012, p. 2).
Other processes expected to be
affected by projected warming include
temperatures, rainfall (amount, seasonal
timing, and distribution), and storms
(frequency and intensity) (see
‘‘Environmental Stochasticity,’’ below).
Models where sea level temperatures are
increasing also show a higher
probability of more intense storms
(Maschinski et al. 2011, p. 148). The
Massachusetts Institute of Technology
(MIT) modeled several scenarios
combining various levels of SLR,
temperature change, and precipitation
differences with human population
growth, policy assumptions, and
conservation funding changes (see
‘‘Alternative Future Landscape
Models,’’ below). All of the scenarios,
from small climate change shifts to
major changes, indicate significant
effects on coastal Miami-Dade County.
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The Science and Technology Committee
of the Miami-Dade County Climate
Change Task Force (Wanless et al. 2008,
p. 1) recognizes that significant SLR is
a serious concern for Miami-Dade
County in the near future. In a January
2008 statement, the committee warned
that sea level is expected to rise at least
0.9–1.5 m (3.0–5.0 ft) within this
century (Wanless et al. 2008, p. 3). With
a 0.9–1.2 m (3.0–4.0 ft) rise in sea level
(above baseline) in Miami-Dade County,
spring high tides would be at about
1.83–2.13 m (6.0–7.0 ft); freshwater
resources would be gone; the Everglades
would be inundated on the west side of
Miami-Dade County; the barrier islands
would be largely inundated; storm
surges would be devastating to coastal
habitat and associated species; and
landfill sites would be exposed to
erosion, contaminating marine and
coastal environments. Freshwater and
coastal mangrove wetlands will be
unable to keep up with or offset SLR of
0.61 m (2.0 ft) per century or greater.
With a 1.52-m (5.0-ft) rise, Miami-Dade
County will be extremely diminished
(Wanless et al. 2008, pp. 3–4).
Prior to inundations from SLR, there
will likely be habitat transitions related
to climate change, including changes to
hydrology and increasing vulnerability
to storm surge. Hydrology has a strong
influence on plant distribution in
coastal areas (IPCC 2008, p. 57). Such
communities typically grade from salt to
brackish to freshwater species. From the
1930s to 1950s, increased salinity of
coastal waters contributed to the decline
of cabbage palm forests in southwest
Florida (Williams et al. 1999, pp. 2056–
2059), expansion of mangroves into
adjacent marshes in the Everglades
(Ross et al. 2000, pp. 101, 111), and loss
of pine rockland in the Keys (Ross et
al.1994, pp. 144, 151–155). In Florida,
pine rocklands transition into rockland
hammocks, and, as such, these habitat
types are closely associated in the
landscape. A study conducted in one
pine rockland location in the Florida
Keys (with an average elevation of 0.89
m (2.90 ft)) found an approximately 65
percent reduction in an area occupied
by South Florida slash pine over a 70year period, with pine mortality and
subsequent increased proportions of
halophytic (salt-loving) plants occurring
earlier at the lower elevations (Ross et
al. 1994, pp. 149–152). During this same
time span, local sea level had risen by
15 cm (6 in), and Ross et al. (1994, p.
152) found evidence of ground water
and soil water salinization.
Extrapolating this situation to
hardwood hammocks is not
straightforward, but it suggests that
changes in rockland hammock species
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composition may not be an issue in the
immediate future (5–10 years); however,
over the long term (within the next 10–
50 years), it may be an issue if current
projections of SLR occur and freshwater
inputs are not sufficient to maintain
high humidities and prevent changes in
existing canopy species through
salinization (Saha et al. 2011, pp. 22–
25). Ross et al. (2009, pp. 471–478)
suggested that interactions between SLR
and pulse disturbances (e.g., storm
surges) can cause vegetation to change
sooner than projected based on sea level
alone. Patterns of human development
will also likely be significant factors
influencing whether natural
communities can move and persist
(IPCC 2008, p. 57; USCCSP 2008,
p. 7–6).
Impacts from climate change,
including regional SLR, have been
studied for coastal hammocks, but not
rockland hammock habitat. Saha (et al.
2011, pp. 24–25) conducted a risk
assessment on rare plant species in ENP
and found that impacts from SLR have
significant effects on imperiled taxa.
This study also predicted a decline in
the extent of coastal hammocks with
initial SLR, coupled with a reduction in
freshwater recharge volume and an
increase in pore water (water filling
spaces between grains of sediment)
salinity, which will push hardwood
species to the edge of their drought
(freshwater shortage and physiological)
tolerance, jeopardizing critically
imperiled and/or endemic species with
possible extirpation. In south Florida,
SLR of 1–2 m (0.30–0.61 ft) is estimated
by 2100, which is on the higher end of
global estimates for SLR. These
projected increases in sea level pose a
threat to coastal plant communities and
habitats from mangroves at sea level to
salinity-intolerant, coastal rockland
hammocks where elevations are
generally less than 2.00 m (6.1 ft) above
sea level (Saha et al. 2011, p. 2). Loss
or degradation of these habitats can be
a direct result of SLR or a combination
of several other factors, including
diversion of freshwater flow, hurricanes,
and exotic plant species infestations,
which can ultimately pose a threat to
rare plant populations (Saha et al. 2011,
p. 24).
Saha (et al. 2011, p. 4) suggested that
the rising water table accompanying
SLR will shrink the vadose zone (the
area that extends from the top of the
ground surface to the water table);
increase salinity in the bottom portion
of the freshwater lens (a convex layer of
fresh ground water that floats on top of
denser saltwater), thereby increasing
brackishness of plant-available water;
and influence tree species composition
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of hardwood hammocks based upon
species-level tolerance to salinity and/or
drought. Evidence of population
declines and shifts in rare plant
communities, along with multi-trophic
effects, already have been documented
on the low-elevation islands of the
Florida Keys (Maschinski et al. 2011, p.
148). Altered freshwater inputs can lead
to the disappearance or decline of
critically imperiled coastal plant
species. Shifts in freshwater flows,
annual precipitation, and variability in
SLR can impact salinity regimes.
Although it is unknown if salinity
changes will impact existing habitat
where T. p. ssp. floridanum currently
lives, it should be noted that salinityintolerant plants can become stressed
within a few weeks from exposure to
saline conditions, and persistent
conditions can promote colonization by
more salinity-tolerant species, thereby
leading to an irreversible composition
change, even if the salinity is lower over
subsequent years (Saha et al. 2011, p.
23).
In some areas of south Florida,
precipitation is the main source of fresh
water. Predictive climate change models
demonstrate periods of drought will
pose a threat to existing populations of
Trichomanes punctatum ssp.
floridanum. Saha (et al. 2011, pp. 19–
21) found that during times of drought
and resultant salinity stress, coastal
hardwood tree density from the canopy
was lost, while other species showed an
increase. Areas with a deeper freshwater
lens, such as rockland hammocks, may
be able to sustain vegetation during
periods of drought; however, whether
this theory is true is currently unknown.
Some tree species in coastal hammocks
have the ability to access pockets of
fresh water and tolerate mild salinities.
These initial responses to salinity
increases may trigger responses similar
to drought, while prolonged exposure
may cause irreversible toxicity caused
by accumulation of salts (Munns 2002,
p. 248), causing a reduction in canopy
or mortality (Maschinski et al. 2009,
entire paper). Impacts from climate
change causing shifts in local plant
communities and invasion of additional
nonnative plant species may be lessened
by the ability of hardwood hammocks
(such as rockland hammocks) to harvest
rainfall water and retain it in the highly
organic soil and lower their
transpiration (i.e., the process of water
movement through a plant and its
evaporation from leaves and stems)
during the dry season (Saha et al. 2011,
p. 24).
Drier conditions and increased
variability in precipitation associated
with climate change are expected to
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hamper successful regeneration of
forests and cause shifts in vegetation
types through time (Wear and Greis
2012, p. 39). With regard to
Trichomanes punctatum ssp.
floridanum, any weather shifts causing
less precipitation would likely impact
the viability of existing populations and
could potentially limit future
reproduction if droughts were to
become a common occurrence.
Ecosystem shifts would result in
rockland and mesic hammocks having
drier conditions, regular droughts, and
changes in humidity, temperature, and
canopy. Increases in the scale,
frequency, or severity of droughts and
wildfires (see ‘‘Fires’’ section, below)
could have negative effects on this taxon
considering its general vulnerability due
to small population size, restricted
range, few populations, and relative
isolation.
Climate change impacts specifically
for Trichomanes punctatum ssp.
floridanum may be numerous and vary
depending on factors such as severity,
the speed at which climate changes
occur, timing, health of the species, and
habitat and tolerance of species. Overall,
management of healthy ecosystems can
support greater biodiversity, which is
considered one of the best strategies to
combat impacts of climate change.
Removing nonnative plants and
minimizing natural disturbance impacts
and other external stresses can improve
the subspecies’ response to climate
change impacts (Maschinski et al. 2011,
p. 159). In general, the best ways to
prepare and protect rare species, such as
T. p. ssp. floridanum, from impacts of
climate change include actively
managing habitats to improve
population growth and potential for
natural dispersal, and controlling for
nonnative species. Efforts to actively
manage for T. p. ssp. floridanum are
currently limited for both
metapopulations due to logistical
feasibility (e.g., dense forest, difficulty
locating populations), insufficient
funding and research, small and
fragmented existing populations, and
lack of successful reintroduction efforts
into the wild.
Alternative Future Landscape Models
To accommodate the high uncertainty
in SLR projections, researchers must
estimate effects from a range of
scenarios. Various model scenarios
developed at MIT and GeoAdaptive Inc.
have projected possible trajectories of
future transformation of the peninsular
Florida landscape by 2060 based upon
four main drivers: Climate change, shifts
in planning approaches and regulations,
human population change, and
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variations in financial resources for
conservation (Vargas-Moreno and
Flaxman 2010, pp. 1–6). The scenarios
do not account for temperature,
precipitation, or species habitat shifts
due to climate change, and no storm
surge effects are considered. The current
MIT scenarios in Florida range from an
increase in sea level of 0.09–1.0 m (0.3–
3.3 ft) by 2060.
Based on the most recent estimates of
SLR and the best available data at this
time, we evaluated potential effects of
SLR using the current ‘‘worst case’’ (e.g.,
the highest range for SLR) MIT scenario,
as well as comparing elevations of
remaining rockland hammock fragments
in Miami-Dade County and mesic
hammocks in Sumter County with
extant populations of Trichomanes
punctatum ssp. floridanum. The ‘‘worst
case’’ MIT scenario assumes SLR of 1.0
m (3.3 ft) by 2060, low financial
resources, a ‘business as usual’
approach to planning, and a doubling of
human population.
Based on the 1.0-m (3.3-ft) scenario,
none of the rockland hammocks in
Miami-Dade County where extant
populations of Trichomanes punctatum
ssp. floridanum occur would be
inundated. However, all four
populations would be within 9.66 km
(6.0 mi) of saltwater, increasing the
likelihood of localized vegetation shifts
within the rockland hammocks and
vulnerability to natural stochastic
events such as hurricanes and tropical
storms. The 1.0-m SLR scenario shows
existing rockland hammocks in MiamiDade County (that do not contain T.p.
ssp. floridanum) directly adjacent to
saltwater. Although these existing
hammocks are located in higher
elevation areas along the coastal ridge,
changes in the salinity of the water table
and soils, along with additional
vegetation shifts in the region, are
likely. A few remaining rockland
hammocks further inland (e.g., Big and
Little George Hammocks) are located in
highly urbanized areas; these hammocks
are small and fragmented, reducing the
chances of further development due to
SLR in the area. Actual impacts may be
greater or less than anticipated based
upon the high variability of factors
involved (e.g., SLR, human population
growth) and the assumptions made in
this model.
A projected SLR (using elevation data)
of 2.0 m (6.6 ft) appears to inundate
much larger portions of urban MiamiDade County. This evaluation was not
based on any modeling, as opposed to
the previous 1.0-m scenario; rather, this
scenario examines current elevation
based on LiDAR (remote sensing
technology that measures distance by
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illuminating a target with a laser and
analyzing the reflected light) data.
Under this 2.0-m (6.6-ft) SLR scenario,
none of the four hammocks where
Trichomanes punctatum ssp.
floridanum is known to occur will be
inundated, but all will be within
approximately 2.41 km (1.5 mi) of
saltwater in the inundated transverse
glades joining the enlarged Biscayne
Bay. Castellow Hammock will be the
least impacted at approximately 2.41 km
(1.5 mi) from saltwater, while Hattie
Bauer will be adjacent to saltwater.
Fuchs and Meissner hammocks will be
1.61 km (1.0 mi) from saltwater and will
be surrounded by more wetlands. This
scenario will leave all these locations
extremely vulnerable to vegetation
shifts, natural stochastic events, and
loss of existing habitat and land
protection. Of the remaining rockland
hammocks not containing T.p. ssp.
floridanum in south Florida, most
would be fully or partially inundated
after a 2.0-m (6.6-ft) SLR, except for the
hammocks located on the higher
elevated coastal ridge, which would still
be adjacent to saltwater.
Due to the higher elevation and
inland location of Sumter County in
north Florida, existing populations of
Trichomanes punctatum ssp.
floridanum and associated habitat will
not be impacted by 1.0- and 2.0-m (3.3and 6.6-ft) rises in sea level. The 2.0-m
(6.6-ft) SLR scenario would still leave
the Sumter occurrences approximately
37.0 km (23.0 mi) from saltwater.
Regional shifts in water table salinity,
soils, or vegetation are not expected.
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Environmental Stochasticity
Endemic species whose populations
exhibit a high degree of isolation, such
as Trichomanes punctatum ssp.
floridanum, are extremely vulnerable to
extinction from both random and
nonrandom catastrophic natural or
human-caused events. Small
populations of species, without positive
growth rates, are considered to have a
high extinction risk from site-specific
demographic (variability in population
growth rates arising from random
differences among individuals in
survival and reproduction within a
season) and environmental
(unpredictable changes in
environmental conditions such as
weather, food supply, or predators)
stochasticity (Lande 1993, pp. 911–927).
Populations at the edge of a species’
range, as may be the case with T.p. ssp.
floridanum in Sumter County, may be
particularly vulnerable to
environmental stochasticity, as they
may also be at the edge of their
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physiological and adaptive limits
(Baguette 2004, p. 216).
The climate in Florida is driven by a
combination of local, regional, and
global events, regimes, and oscillations
˜
(e.g., El Nino Southern Oscillation with
a frequency of every 4 to 7 years, solar
cycle every 11 years, and the Atlantic
Multi-decadal Oscillation); however, the
exact magnitude, direction, and
distribution of these climatic influences
on a regional level are difficult to
project. There are three main ‘‘seasons’’
in Florida: (1) The wet season, which is
hot, rainy, and humid from June
through October; (2) the official
hurricane season that extends 1 month
beyond the wet season (June 1 through
November 30), with peak season being
August and September; and (3) the dry
season, which is drier and cooler, from
November through May (Miller 2013,
pers. comm.). In the dry season,
periodic surges of cool and dry
continental air masses influence the
weather with short-duration rain events
followed by long periods of dry weather.
Florida is considered the most
vulnerable State in the United States to
hurricanes and tropical storms (Florida
Climate Center, https://coaps.fsu.edu/
climate_center). Based on data gathered
from 1856 to 2008, Klotzbach and Gray
(2009, p. 28) calculated the
climatological probabilities for each
State being impacted by a hurricane or
major hurricane in all years over the
152-year timespan. Of the coastal States
analyzed, Florida had the highest
climatological probabilities, with a 51
percent probability of a hurricane
(Category 1 or 2) and a 21 percent
probability of a major hurricane
(Category 3 or higher). From 1856 to
2008, Florida experienced 109
hurricanes and 36 major hurricanes.
Given the few isolated populations and
restricted range of Trichomanes
punctatum ssp. floridanum in locations
prone to storm influences (i.e., MiamiDade County), this subspecies is at
substantial risk from hurricanes, storm
surges, and other extreme weather
events.
Natural stochastic events can pose a
threat to the persistence of Trichomanes
punctatum ssp. floridanum through the
destruction of existing habitat. Some
climate change models predict
increased frequency and duration of
severe storms, including hurricanes and
tropical storms (McLaughlin et al. 2002,
p. 6074; Cook et al. 2004, p. 1015;
Golladay et al. 2004, p. 504). Other
models predict that hurricane and
tropical storm frequencies in the
Atlantic will decrease between 10–30
percent by 2100 (Knutson et al. 2008,
pp. 1–21). For those models that predict
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fewer hurricanes, hurricane wind
speeds are expected to increase by 5–10
percent due to an increase in available
energy for intense storms. Increases in
hurricane winds can elevate the chances
of damage to existing canopy.
In south Florida, tropical hardwood
hammock forests are known to
experience frequent disturbances from
hurricanes (Horvitz et al. 1998, p. 947).
Hurricanes and tropical storms can
damage existing canopy, which
provides shade and cover from wind.
Canopy loss of any kind is determined
to be the threat with greatest impact to
existing metapopulations of
Trichomanes punctatum ssp.
floridanum (Adimey 2013b, field notes;
Possley 2013l, pers. comm.). For
example, impacts from Hurricane
Andrew in 1992 may have been
responsible for the temporary loss of the
subspecies from Hattie Bauer Hammock,
where it had been observed for many
years. Following this hurricane, the
canopy was damaged, allowing
increased exposure to sunlight for
several years. T.p. ssp. floridanum was
not seen again in Hattie Bauer
Hammock until 2011 (Possley 2013l,
pers. comm.). Through natural recovery,
assisted by active management activities
by the EEL Program and PROS–NAM, a
large portion of the Hattie Bauer
Hammock canopy has been restored to
pre-hurricane Andrew conditions
(Guerra 2014, pers. comm.). Destruction
of habitat due to hurricanes has also
been documented in Sumter County in
the Indian Ledges Hammock located
near the town of Wahoo. This hammock,
known to host a variety of rare ferns,
orchids, and large trees, sustained
severe damage from several hurricanes
in 2004; very few native plant species
once found in Indian Ledges Hammock
exist in this location today (Deangelis
2014a, pers. comm.).
Historically, Trichomanes punctatum
ssp. floridanum may have benefitted
from more abundant and contiguous
habitat to buffer it from storm events.
The destruction and modification of
native habitat, combined with the
subspecies’ small population sizes, has
likely contributed over time to the
stress, decline, and, in some instances,
extirpation of populations or local
occurrences due to stochastic events.
A study conducted by Horvitz et al.
(1998, p. 947) found that the
regeneration of forest species after
stochastic events depended on the
amount of canopy disturbance, the time
since disturbance, and the biological
relationship between the individual
species and its environment. Following
Hurricane Andrew, the relative
abundance and life stage changed for
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many nonnative plant species within
Miami-Dade County. These shifts
continued to occur as a result of
subsequent stochastic events, suggesting
hurricanes can alter long-term hammock
structure and the ongoing changes in
species composition (Horvitz et al.
1998, pp. 961, 966).
Stochastic events resulting in changes
in normal precipitation (amount,
seasonal timing, and distribution) and
extreme temperature fluctuations may
also impact Trichomanes punctatum
ssp. floridanum. During the winter dry
season, T.p. ssp. floridanum can become
desiccated without periodic rainfall and
then recover during the wet season.
Multiyear droughts may negatively
impact populations. While droughts are
natural events, they are a threat because
there are so few populations of this
subspecies. Specific parameters
regarding humidity, temperature, and
precipitation requirements are not
known at this time for T.p. ssp.
floridanum, making it difficult to
accurately determine what impacts will
occur from modifications in current
environmental conditions where extant
metapopulations occur. Extreme
temperature changes such as cold events
in south Florida or freezing
temperatures in central Florida could
have devastating impacts on this
subspecies. The small size of each
population makes this plant especially
vulnerable, in which the loss of even a
few individuals could reduce the
viability of a single population.
Due to the small size of existing
populations of Trichomanes punctatum
ssp. floridanum and its limited genetic
variability, the subspecies’ overall
ability to respond and adapt to threats
is likely low. These factors, combined
with additional stress from habitat
modifications (e.g., hydrological
changes) may increase the inherent risk
posed by stochastic events that impact
this subspecies (Matthies et al. 2004, pp.
481–488). Additionally, stochastic
events are expected to exacerbate the
impacts of regional drainage and
subsequent drops in humidity. For these
reasons, T.p. ssp. floridanum is at risk
of extirpation during extreme stochastic
events. We have determined that these
natural stochastic events coupled with
existing small population sizes, as
addressed above, are a threat to the
subspecies (Adimey 2013b, field notes;
Possley 2013l, pers. comm.).
Fires
Although fires are not a current
concern for existing populations of
Trichomanes punctatum ssp.
floridanum, they have been known to
impact populations in the past.
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Craighead (1963, p. 39) noted that
extensive fires in hammocks eliminated
ferns in much of their former range.
Drainage efforts in the early 1900s also
increased the occurrence of fire, as
lands became drier. Phillips (1940, p.
166) noted that the frequent occurrence
of fires in the late 1930s in southern
Florida resulted in widespread
destruction of flora. Fires may have
been a factor in the disappearance of
this taxon in Royal Palm Hammock,
which suffered multiple fires in the first
half of the 1900s according to
photographs from J.K. Small (1917;
Florida Memory, State Library and
Archives of Florida; Tallahassee,
Florida). In recent decades, wildfires
have been controlled in most rockland
hammocks due to the extensive
urbanization in Miami-Dade County.
However, fires do have the potential to
impact T.p. ssp. floridanum during
periods of prolonged drought. While
fires are a natural component of some
ecosystems in south Florida, fires in
hammocks can set back succession to
pine rockland or other communities and
will directly kill many plant species that
are not adapted to fires, such as T.p. ssp.
floridanum.
Generally, hammock environments
are considered less susceptible to
wildfires because their shaded, humid
microclimate is not conducive to fire
spread (Snyder et al. 1990, p. 258).
Additionally, rockland hammocks
occupy elevated, rarely inundated, and
fire-free sites in all three of the major
rockland areas in south Florida (Snyder
et al. 1990, p. 239). Mesic hammocks are
also considered fire resistant in that
many occur as ‘‘islands’’ on high ground
within basin or floodplain wetlands, as
patches of oak/palm forest in dry prairie
or flatwoods communities, on river
levees, or in ecotones between wetlands
and upland communities, and possess
high-moisture soils due to heavy
shading of the ground layer and
accumulation of litter (FNAI 2010, p.
20). Additionally, wildfires are now
considered a minor stressor in mesic
hammocks because of the use of
prescribed burns within the last 15
years (Werner 2013d, pers. comm.).
Snyder (et al. 1990, p. 238) points out
that the high organic content of
hammock soils in south Florida can
enable the soil to burn; however, soil
fires typically only burn in hammocks
in times of drought or when fires are
intentionally set (Snyder et al. 1990, pp.
258–260). This stressor is considered
minimal in that fires typically will go
out when they reach hammock margins,
whether entering from pineland or some
other community due to the presence of
hardwood leaf litter lying directly on
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moist organic soil with minimal
herbaceous fuel.
Although wildfires are known to
occur in Miami-Dade and Sumter
Counties, they are not currently
considered a threat at this time due to
regional prescribed burn efforts that
help minimize the occurrence of
wildfires, the natural fire-resistant
features of these two habitats, and, in
Sumter County, hydric hammock (less
likely to burn) surrounding
Trichomanes punctatum ssp.
floridanum populations.
Public Use/Encroachment
In Miami-Dade County, two of the
four hammocks containing Trichomanes
punctatum ssp. floridanum (Castellow
and Hattie Bauer) are accessible to the
public. However, in both cases, T.p. ssp.
floridanum is not accessible from the
nature trail (Possley 2013g, pers.
comm.). If public use were to increase
significantly at any of the Miami-Dade
hammocks, populations of T.p. ssp.
floridanum could become at risk. For
example, because the taxon grows along
the rim and walls of solution holes,
people climbing into these holes could
damage existing populations; increased
use could also introduce additional
nonnative seed sources into the habitat.
Similarly, climbing on boulders where
the fern occurs in Sumter County could
also cause damage. However, due to the
low amount of visitation at the
Withlacoochee State Forest (Werner
2013b–c, pers. comm.), public use and
encroachment do not appear to be
occurring at this time, and we have
determined they do not pose a threat to
T.p. ssp. floridanum.
Small Population Size Effects and
Isolation
Small, isolated populations are more
susceptible to impacts overall, and
relatively more vulnerable to extinction
due to genetic problems, demographic
and environmental fluctuations, and
natural catastrophes (Primack 1993, p.
255). That is, the smaller a population
becomes, the more likely it is that one
or more stressors could impact a
population, potentially reducing its size
such that it is at increased risk of
extinction. Although robust population
viability analyses (including minimum
viable population calculations) have not
been conducted for this subspecies,
indications are that most existing
populations are minimal in terms of
abundance and size. Lack of dispersal
between occurrences also contributes to
the low resilience for this subspecies
(see ‘‘Habitat Fragmentation’’ under
Factor A).
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Limited genetic variability will also
impact Trichomanes punctatum ssp.
floridanum populations. The ability of a
species to adapt to environmental
change is dependent upon genetic
variation, a property of populations that
derives from its members possessing
different forms (i.e., alleles) of the same
gene (Primack 1998, p. 283). High
genetic diversity can enhance a species’
persistence in a changing environment
(Lynch and Lande 1993, pp. 246–247).
Although Trichomanes punctatum ssp.
floridanum can grow in clusters,
separate clusters are not necessarily
different individuals, as they may have
been connected by one or more stems in
the past (Possley 2014b, pers. comm.).
Thus, a population of T.p. ssp.
floridanum containing many clusters
may not have greater genetic diversity
than a population with few clusters.
Because there are only six extant
populations of T.p. ssp. floridanum,
each with few plants, the genetic
variability is considered low, and the
subspecies is inherently at greater risk
from stochastic events and changes in
environmental conditions (Matthies et
al. 2004, pp. 481–488).
In summary, Trichomanes punctatum
ssp. floridanum is impacted by factors
such as small population size,
vulnerability to random demographic
fluctuations or natural catastrophes, and
low genetic diversity, which is further
magnified by synergistic (interaction of
two or more components) effects with
other threats, such as those discussed
above. In evaluating the stressor of small
population size effects on Trichomanes
punctatum ssp. floridanum, we
reviewed the limited data available
concerning abundance at each of the
occurrences across the subspecies’
range. This represents a conservative
classification of small population size,
as available data do not discriminate
among individual plants and life-history
stages. These small populations are at
risk of adverse effects from reduced
genetic variation, an increased risk of
inbreeding depression, and reduced
reproductive output. Many of these
populations are small and isolated from
each other, decreasing the likelihood
that they could be naturally
reestablished in the event that
extirpation from one location occurs.
Conservation Efforts To Reduce Other
Natural or Manmade Factors Affecting
Its Continued Existence
Miami-Dade County and the State of
Florida have ongoing nonnative plant
management programs to reduce threats
on public lands, as funding and
resources allow. In Miami-Dade County,
nonnative, invasive plant management
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is very active, with a goal to treat all
publically owned properties at least
once a year and more often in many
cases. Annual monitoring of
Trichomanes punctatum ssp.
floridanum is conducted by Fairchild,
which records health and size of
individual clusters of the subspecies
along with potential new stressors,
including nonnative, invasive species or
habitat destruction; reports are
forwarded to the County preserve
managers for further attention (Possley
2013l, pers. comm.). IRC also conducts
research and monitoring in multiple
hammocks within Miami-Dade County
for various rare and endangered plant
species. Nonnative, invasive species are
documented, along with any occurrence
of human disturbance (van der Heiden
2013i, pers. comm.). In Sumter County,
the Florida Park Service surveys each
State-owned property at least once a
year to manage for nonnative plants
(Werner 2013a–b, pers. comm.).
Furthermore, Withlacoochee State
Forest conducts prescribed burning on
an annual basis, controlling regional
wildfires in dry swamps and mesic
hammocks.
Continuing efforts to propagate
Trichomanes punctatum ssp.
floridanum in-vitro may eventually lead
to the establishment of healthy
populations that can be reintroduced in
locations where the taxon once occurred
or introduced to new areas deemed
appropriate. These efforts can assist
with combating potential or realized
impacts from natural stochastic events
that may harm or destroy existing
populations.
Summary of Factor E
Stochastic events resulting in changes
in canopy structure and environmental
conditions within the taxon’s current
habitat are considered threats to existing
and future populations of T.p. ssp.
floridanum. Droughts, tropical storms,
and hurricanes are common occurrences
in Florida, and changes associated with
these events have the potential to limit
reproduction and compromise overall
health in the long term, making plants
more vulnerable to other stressors (e.g.,
periodic, long-term droughts,
hurricanes) or causing extirpations. As
few populations remain, the entire
taxon is at risk of extinction during
these events. Climatic changes,
including SLR, are longer term concerns
expected to exacerbate existing impacts
and ultimately reduce the extent of
available habitat for T.p. ssp.
floridanum.
The presence of nonnative species,
including other plants and feral hogs, is
also a threat, but may be reduced on
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public lands due to active programs by
Miami-Dade County and the State. The
majority of the remaining populations of
this plant are small and geographically
isolated, and genetic variability is likely
low, increasing the inherent risk due to
overall low resilience of this subspecies.
Furthermore, the isolated existence of
Trichomanes punctatum ssp.
floridanum makes natural
recolonization of extirpated populations
virtually impossible without human
intervention. Although considered
stressors, wildfires and public use at
extant sites are minimal and do not rise
to the level of a threat.
Cumulative Effects of Threats
When two or more threats affect
Trichomanes punctatum ssp.
floridanum occurrences, the effects of
those threats could interact or become
compounded, producing a cumulative
adverse effect that is greater than the
impact of either threat alone. The most
obvious cases in which cumulative
adverse effects would be significant are
those in which small populations
(Factor E) are affected by threats that
result in destruction or modification of
habitat (Factor A). The limited
distributions and small population sizes
of T.p. ssp. floridanum make it
extremely susceptible to the detrimental
effects of further habitat modification,
degradation, and loss, as well as other
anthropogenic threats. Mechanisms
leading to the decline of this taxon, as
discussed above, range from local (e.g.,
hydrology changes, agriculture) to
regional (e.g., development,
fragmentation, nonnative species) to
global influences (e.g., climate change,
SLR). The synergistic effects of threats,
such as impacts from hurricanes on a
species with a limited distribution and
small populations, make it difficult to
predict population viability. While
these stressors may act in isolation, it is
more probable that many stressors are
acting simultaneously (or in
combination) on populations of T.p. ssp.
floridanum, making this subspecies
more vulnerable.
Determination
We have carefully assessed the best
scientific and commercial data available
regarding the past, present, and future
threats to Trichomanes punctatum ssp.
floridanum. T.p. ssp. floridanum has
been extirpated from the majority of its
historical range, and the primary threats
of habitat destruction and modification
resulting from human population
growth and development, agricultural
conversion, regional drainage, and
resulting changes in canopy and
hydrology (Factor A); competition from
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nonnative, invasive species (Factor E);
changes in climatic conditions,
including sea level rise (Factor E); and
natural stochastic events (Factor E)
remain threats for existing populations.
Existing regulatory mechanisms have
not led to a reduction or removal of
threats posed to the subspecies from
these factors (see Factor D discussion).
These threats are ongoing, rangewide,
and expected to continue in the future.
Populations of T.p. ssp. floridanum are
relatively small and isolated from one
another, and their ability to recolonize
suitable habitat is unlikely without
human intervention. Because of the
current condition of the extant
populations and life-history traits of the
subspecies, it is vulnerable to natural or
human-caused changes in its currently
occupied habitats. The threats have had
and will continue to have substantial
adverse effects on T.p. ssp. floridanum
and its habitat. Although attempts are
ongoing to alleviate or minimize some
of these threats at certain locations, all
populations appear to be impacted by
one or more threats.
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 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.’’ As
described in detail above, this plant is
currently at risk throughout all of its
range due to the immediacy, severity,
significance, timing, and scope of those
threats. Impacts from these threats are
ongoing and increasing; singly or in
combination, these threats place the
subspecies in danger of extinction. The
risk of extinction is high because the
populations are small, isolated, and
have limited to no capacity for
recolonization. Numerous threats are
currently ongoing and are likely to
continue in the foreseeable future, at a
high intensity and across the entire
range of this subspecies. Furthermore,
natural stochastic events and changes in
climatic conditions pose a threat to the
persistence of the subspecies, especially
because mitigation measures have yet to
be developed. Individually and
collectively, all of these threats can
contribute to the local extirpation and
potential extinction of this subspecies.
Because these threats are placing this
subspecies in danger of extinction
throughout its range, we have
determined this plant meets the
definition of an endangered species.
Therefore, on the basis of the best
available scientific and commercial
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information, we are listing Trichomanes
punctatum ssp. floridanum as an
endangered species in accordance with
sections 3(6) and 4(a)(1) of the Act. We
find that a threatened species status is
not appropriate for T.p. ssp. floridanum
because of the contracted range of the
subspecies and because the threats are
occurring rangewide, are currently
acting on the subspecies at a high
intensity, and are expected to continue
into the future.
Significant Portion of the 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. Because we have determined
that Trichomanes punctatum ssp.
floridanum is an endangered species
throughout all of its range, no portion of
its range can be ‘‘significant’’ for
purposes of the definitions of
‘‘endangered species’’ and ‘‘threatened
species.’’ See the Final Policy on
Interpretation of the Phrase ‘‘Significant
Portion of Its Range’’ in the Endangered
Species Act’s Definitions of
‘‘Endangered Species’’ and ‘‘Threatened
Species’’ (79 FR 37578, July 1, 2014).
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened species under the Act
include recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness and conservation by
Federal, State, Tribal, and local
agencies, private organizations, and
individuals. The Act encourages
cooperation with the States and requires
that recovery actions be carried out for
all listed species. The protection
required by Federal agencies and the
prohibitions against certain activities
are discussed, in part, below.
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Subsection 4(f) of
the Act requires the Service to develop
and implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse the species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, self-
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sustaining, and functioning components
of their ecosystems.
Recovery planning includes the
development of a recovery outline
shortly after a species is listed and
preparation of a draft and final recovery
plan. The recovery outline guides the
immediate implementation of urgent
recovery actions and describes the
process to develop a recovery plan. The
plan may be revised to address
continuing or new threats to the species,
as new substantive information becomes
available. The recovery plan identifies
recovery criteria for review of when a
species may be ready for downlisting
(from endangered species to threatened
species) or delisting 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 (composed of species
experts, Federal and State agencies,
nongovernmental organizations, and
stakeholders) are often established to
develop recovery plans. When
completed, the draft and final recovery
plans will be available on our Web site
(https://www.fws.gov/endangered) or
from our South Florida 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, Tribes,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private, State, and Tribal lands.
Following publication of this final
listing rule, funding for recovery actions
will be available from a variety of
sources, including Federal budgets,
State programs, and cost share grants for
non-Federal landowners, the academic
community, and nongovernmental
organizations. In addition, pursuant to
section 6 of the Act, the State of Florida
will be eligible for Federal funds to
implement management actions that
promote the protection or recovery of
Trichomanes punctatum ssp.
floridanum. Information on our grant
programs that are available to aid
species recovery can be found at:
https://www.fws.gov/grants.
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Please let us know if you are
interested in participating in recovery
efforts for Trichomanes punctatum ssp.
floridanum. Additionally, we invite you
to submit any new information on this
subspecies whenever it becomes
available and any information you may
have for recovery planning purposes
(see FOR FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is listed as an endangered or threatened
species 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)(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 any endangered or
threatened species or destroy or
adversely modify its critical habitat. If a
Federal action may affect a listed
species or its critical habitat, the
responsible Federal agency must enter
into consultation with the Service.
Federal agency actions within the
species’ habitat that may require
conference or consultation, or both, as
described in the preceding paragraph,
include, but are not limited to, federally
funded or authorized actions such as
habitat restoration and control of
nonnatives management and any other
landscape-altering activities on Federal
lands administered by the U.S. Fish and
Wildlife Service; issuance of section 404
Clean Water Act permits by the Army
Corps of Engineers; and construction
and maintenance of roads or highways
by the Federal Highway Administration.
With respect to endangered plants, 50
CFR 17.61 makes 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 to remove and
reduce to possession any such plant
species from areas under Federal
jurisdiction. In addition, for endangered
plants, the Act prohibits malicious
damage or destruction of any such
species on any area under Federal
jurisdiction, and the removal, cutting,
digging up, or damaging or destroying of
any such species on any other area in
knowing violation of any State law or
regulation, or in the course of any
violation of a State criminal trespass
law. Exceptions to these prohibitions
are contained in 50 CFR 17.62.
We may issue permits to carry out
otherwise prohibited activities
involving endangered plants under
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certain circumstances. Regulations
governing permits are codified at 50
CFR 17.62. With regard to endangered
plants, the Service may issue a permit
authorizing any activity otherwise
prohibited by 50 CFR 17.61 for scientific
purposes or for enhancing the
propagation or survival of endangered
plants.
It is our policy, as published in the
Federal Register on July 1, 1994 (59 FR
34272), to identify to the maximum
extent practicable at the time a species
is listed, those activities that would or
would not constitute a violation of
section 9 of the Act. The intent of this
policy is to increase public awareness of
the effect of a listing on proposed and
ongoing activities within the range of a
listed species. The following activities
could potentially result in a violation of
section 9 of the Act. This list is not
comprehensive:
(1) Import the subspecies into, or
export the subspecies from, the United
States without authorization;
(2) Remove and reduce to possession
the subspecies from areas under Federal
jurisdiction; maliciously damage or
destroy the subspecies on any such area;
or remove, cut, dig up, or damage or
destroy the subspecies on any other area
in knowing violation of any law or
regulation of any State or in the course
of any violation of a State criminal
trespass law;
(3) Sell or offer for sale in interstate
or foreign commerce the subspecies;
except for properly documented antique
specimens of the taxon at least 100 years
old, as defined by section 10(h)(1) of the
Act;
(4) Unauthorized delivering, carrying,
or transporting of the subspecies,
including import or export across State
lines and international boundaries;
(5) Introduction of nonnative species
that compete with or prey upon
Trichomanes punctatum ssp.
floridanum;
(6) Unauthorized release of biological
control agents that attack any life stage
of this subspecies; and
(7) Unauthorized manipulation or
modification of the habitat where
Trichomanes punctatum ssp.
floridanum is present on Federal lands
including, but not limited to,
unauthorized water withdrawal from
solution holes and unauthorized
removal of canopy.
Questions regarding whether specific
activities would constitute a violation of
section 9 of the Act should be directed
to the South Florida Ecological Services
Field Office (see FOR FURTHER
INFORMATION CONTACT).
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Critical Habitat
Section 3(5)(A) of the Act defines
critical habitat as ‘‘(i) the specific areas
within the geographical area occupied
by the species, at the time it is listed
. . . 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 by
the Secretary that such areas are
essential for the conservation of the
species.’’ Section 3(3) of the Act (16
U.S.C. 1532(3)) also defines the terms
‘‘conserve,’’ ‘‘conserving,’’ and
‘‘conservation’’ to mean ‘‘to use and the
use of all methods and procedures
which are necessary to bring any
endangered species or threatened
species to the point at which the
measures provided pursuant to this
chapter are no longer necessary.’’
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 shall
designate critical habitat at the time the
species is determined to be an
endangered or threatened species. 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.
In our proposed listing rule, because
we determined that the designation of
critical habitat will not likely increase
the degree of threat to the species and
may provide some measure of benefit,
we determined that designation of
critical habitat is prudent for
Trichomanes punctatum ssp.
floridanum.
Critical Habitat Determinability
Having determined that designation is
prudent under section 4(a)(3) of the Act,
we must find whether critical habitat for
Trichomanes punctatum ssp.
floridanum is determinable. Our
regulations (50 CFR 424.12(a)(2)) further
state that critical habitat is not
determinable when one or both of the
following situations exists: (1)
Information sufficient to perform
required analysis of the impacts of the
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designation is lacking; or (2) the
biological needs of the species are not
sufficiently well known to permit
identification of an area as critical
habitat.
In our proposed listing rule, we found
that critical habitat was not
determinable because a careful
assessment of the economic impacts that
may occur due to a critical habitat
designation was still ongoing, and we
were still in the process of acquiring the
information needed to perform that
assessment. We have recently received
new data on suitable habitat for T. p.
ssp. floridanum in Sumter County,
which has caused us to begin
reassessing which specific features and
areas are essential for the conservation
of the species and, therefore, meet the
definition of critical habitat.
Consequently, a careful assessment of
the new biological information is still
ongoing, and we are still in the process
of acquiring the information needed to
perform that assessment. The
information sufficient to perform a
required analysis of the impacts of the
designation is lacking, and therefore, we
find designation of critical habitat to be
not determinable at this time.
Accordingly, we will publish a
proposed critical habitat rule when we
finish our assessment of the new
biological information.
Required Determinations
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 (42
U.S.C. 4321 et seq.), need not be
prepared in connection with listing a
species as an endangered or threatened
species under the Endangered Species
Act. We published a notice outlining
our reasons for this determination in the
Federal Register on October 25, 1983
(48 FR 49244).
Government-to-Government
Relationship With Tribes
In accordance with the President’s
memorandum of April 29, 1994
(Government-to-Government Relations
with Native American Tribal
Governments; 59 FR 22951), Executive
Order 13175 (Consultation and
Coordination with Indian Tribal
Governments), and the Department of
the Interior’s manual at 512 DM 2, we
readily acknowledge our responsibility
to communicate meaningfully with
recognized Federal Tribes on a
government-to-government basis. In
accordance with Secretarial Order 3206
of June 5, 1997 (American Indian Tribal
Rights, Federal-Tribal Trust
Responsibilities, and the Endangered
Species Act), we readily acknowledge
our responsibilities to work directly
with tribes in developing programs for
healthy ecosystems, to acknowledge that
tribal lands are not subject to the same
controls as Federal public lands, to
remain sensitive to Indian culture, and
to make information available to tribes.
We are not aware of any Trichomanes
punctatum ssp. floridanum populations
on tribal lands.
References Cited
A complete list of references cited in
this rulemaking is available on the
Internet at https://www.regulations.gov
and upon request from the South
Florida Ecological Services Field Office
(see FOR FURTHER INFORMATION CONTACT).
Authors
The primary authors of this final rule
are the staff members of the South
Florida Ecological Services Field Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Regulation Promulgation
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as follows:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 1531–
1544; 4201–4245; unless otherwise noted.
2. Amend § 17.12(h) by adding an
entry for ‘‘Trichomanes punctatum ssp.
floridanum’’ to the List of Endangered
and Threatened Plants in alphabetical
order under Ferns and Allies to read as
follows:
■
§ 17.12
*
Endangered and threatened plants.
*
*
(h) * * *
Species
Historic range
Scientific name
*
FERNS AND ALLIES
*
Trichomanes
punctatum ssp.
floridanum.
*
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*
*
*
Florida bristle fern ......
*
*
*
*
*
Family
Status
Common name
*
*
*
U.S.A. (FL) .................
*
*
When
listed
*
*
Hymenophyllaceae .....
*
*
859
E
*
*
[FR Doc. 2015–25299 Filed 10–5–15; 8:45 am]
BILLING CODE 4333–15–P
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Critical
habitat
*
Dated: September 28, 2015.
Stephen Guertin,
Acting Director, U.S. Fish and Wildlife
Service.
*
*
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Special
rules
*
*
NA
NA
*
Agencies
[Federal Register Volume 80, Number 193 (Tuesday, October 6, 2015)]
[Rules and Regulations]
[Pages 60439-60465]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-25299]
[[Page 60439]]
Vol. 80
Tuesday,
No. 193
October 6, 2015
Part II
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
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50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Endangered Species
Status for Trichomanes punctatum ssp. floridanum (Florida Bristle
Fern); Final Rule
Federal Register / Vol. 80 , No. 193 / Tuesday, October 6, 2015 /
Rules and Regulations
[[Page 60440]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R4-ES-2014-0044; 4500030113]
RIN 1018-AY97
Endangered and Threatened Wildlife and Plants; Endangered Species
Status for Trichomanes punctatum ssp. floridanum (Florida Bristle Fern)
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), determine
endangered species status under the Endangered Species Act of 1973
(Act), as amended, for Trichomanes punctatum ssp. floridanum (Florida
bristle fern), a plant subspecies from Miami-Dade and Sumter Counties,
Florida. The effect of this regulation will be to add this subspecies
to the Federal List of Endangered and Threatened Plants and extend the
Act's protections to this subspecies.
DATES: This rule becomes effective on November 5, 2015.
ADDRESSES: This final rule is available on the internet at https://www.regulations.gov and https://www.fws.gov/verobeach/. Comments and
materials we received, as well as supporting documentation we used in
preparing this rule, are available for public inspection at https://www.regulations.gov. All of the comments, materials, and documentation
that we considered in this rulemaking are available by appointment,
during normal business hours at: U.S. Fish and Wildlife Service, South
Florida Ecological Services Office, 1339 20th Street, Vero Beach, FL
32960; telephone 772-562-3909.
FOR FURTHER INFORMATION CONTACT: Roxanna Hinzman, Field Supervisor,
U.S. Fish and Wildlife Service, South Florida Ecological Services
Office, 1339 20th Street, Vero Beach, FL 32960, by telephone 772-562-
3909 or by facsimile 772-562-4288. Persons who use a telecommunications
device for the deaf (TDD) may call the Federal Information Relay
Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. Under the Act, a species may warrant
protection through listing if it is endangered or threatened throughout
all or a significant portion of its range. Listing a species as an
endangered or threatened species can only be completed by issuing a
rule. This rule will finalize the listing of the Trichomanes punctatum
ssp. floridanum (Florida bristle fern) as an endangered species.
The basis for our action. Under the Act, we can determine that a
species is an endangered or threatened species based on any of five
factors: (A) The present or threatened destruction, modification, or
curtailment of its habitat or range; (B) Overutilization for
commercial, recreational, scientific, or educational purposes; (C)
Disease or predation; (D) The inadequacy of existing regulatory
mechanisms; or (E) Other natural or manmade factors affecting its
continued existence. We have determined that the threats to Trichomanes
punctatum ssp. floridanum consist primarily of destruction and
modification of habitat (Factor A), proliferation of nonnative invasive
species, natural stochastic events including hurricanes and tropical
storms, and impacts from climate change including temperature shifts
and sea level rise (Factor E), and that existing regulatory mechanisms
have not reduced or removed such threats (Factor D).
Peer review and public comment. We sought comments from independent
specialists to ensure that our designation is based on scientifically
sound data, assumptions, and analyses. We invited these peer reviewers
to comment on our listing proposal. We also considered all comments and
information received during the comment period.
Previous Federal Actions
Please refer to the proposed listing rule for Trichomanes punctatum
ssp. floridanum (79 FR 61136), published on October 9, 2014, for a
detailed description of previous Federal actions concerning this
subspecies.
Our proposed listing rule included a finding that designation of
critical habitat was prudent, but that critical habitat was not
determinable. In this final listing rule, we find that critical habitat
is still not determinable (see Critical Habitat discussion below).
Background
Below we present updated and revised information, based on peer
review and public comment received during the comment period on the
proposed rule, as well as new information, related to the subspecies'
life history, historical and current ranges, and habitat requirements.
Species Description
Trichomanes punctatum ssp. floridanum, commonly referred to as the
Florida bristle fern, is mat-forming, has root-like structures, and
contains trichomes (hairlike/bristlelike outgrowths), which extend from
soral involucres (tubes containing sporangia (an enclosure in which
spores, or reproductive cells, are formed)) on the tips of some fronds
(leaves of ferns) when the plant is fertile (Wunderlin and Hansen 2000,
pp. 153-154). This subspecies is very small in size and superficially
resembles bryophytes, such as mosses and liverworts, making it
difficult to observe in its natural habitat.
Wunderlin and Hansen (2000, pp. 153-154) described Trichomanes
punctatum ssp. floridanum as having leaves, with the petiole (stalk by
which a leaf is attached to a plant) 0.1-2.0 centimeters (cm) (0.04-
0.79 inches (in)) long and typically shorter than the blade. The blade
is fan-shaped, round, entire or irregularly lobed at the apex, and 0.5-
2.0 cm (0.20-0.79 in) long and 0.2-1.1 cm (0.08-0.43 in) wide. T. p.
ssp. floridanum has thin veinlets (small veins) that are not enlarged
towards the margin while true veins are uniform in width to their
apices (tips) (Nauman 1986, p. 179). This subspecies has few false
veins, and fronds are considered simple (Morton 1963, p. 89).
One unusual characteristic of this plant is that it lacks cuticles
(the protective layer that covers the epidermis, which is the outermost
layer of cells that cover the leaves) or has highly reduced cuticles.
The fern has differentiated epidermises and stomata (small openings in
leaves and stems through which gases are exchanged), causing it to be
dependent on elevated moisture conditions because a barrier is not
present to prevent unregulated loss of water (Kr[ouml]mer and Kessler
2006, p. 57). This dependence restricts most Trichomanes ssp. to shaded
areas within forested environments with high humidity, making them more
vulnerable to changes in localized climatic conditions (Schuster 1971,
p. 91; Nauman 1986, pp. 181-182; van der Heiden 2014, p. 5).
Taxonomy
The genus Trichomanes contains approximately 320 species of ferns
that occur primarily in the tropics and for which we generally lack
ecological information (Nauman 1986, p. 179; Nelson 2000, p. 77). The
genus belongs to the family Hymenophyllaceae and the hymenophylloid
clade, where ferns are also referred to as filmy ferns, which
[[Page 60441]]
describes the thin, filmy leaves of the species (Nelson 2000, p. 77).
The common name, bristle fern, is used to reference the bristlelike
structure that singularly protrudes from each soral involucre (a
structure that holds and produces spores) (Nelson 2000, p. 77).
Five species commonly known as bristle ferns (Trichomanes ssp.)
have been found in Florida (Kr[ouml]mer and Kessler 2006, p. 57).
Trichomanes punctatum ssp. floridanum is a subspecies of Trichomanes
punctatum, the current taxonomy of which is the result of monographic
revision of Trichomanes sections (a taxonomic rank or position below
the genus but above the species) Didymoglossum and Microgonium by
Wessels Boer (1962, pp. 300-301). All U.S. species of Trichomanes now
belong to the section Didymoglossum, except T. boschianum (Morton
1963). Wessels Boer, in reviewing specimens from throughout the
American tropics, determined that all Trichomanes punctatum plants in
Florida represented the same taxon, not two separate species, and that
T. sphenoides (which he described as T. punctatum ssp. sphenoides) does
not occur in Florida. He further determined that Trichomanes punctatum
plants in Florida were different from those in the tropics and
described them as a new subspecies, Trichomanes punctatum ssp.
floridanum (Boer 1962, pp. 300-301). This treatment has been followed
by almost all subsequent authors (Lakela and Long 1976, p. 53;
Wunderlin 1982, p. 32; Lellinger 1985, p. 205; Nauman 1986, p. 181;
Flora of North America Editorial Committee 1993, p. 196; Wunderlin
1998, p. 44; Nelson 2000, p. 81; Wunderlin and Hansen 2000, p. 153;
Wunderlin and Hansen 2003, p. 44). The only exception is Long and
Lakela (1971, p. 73), who treated the subspecies as T. punctatum
without further explanation. Additionally, the following entities use
the name T. p. ssp. floridanum and indicate that this subspecies'
taxonomic standing is accepted:
Florida Department of Agriculture and Consumer Services
(2013, https://www.flrules.org/gateway/RuleNo.asp?title=PRESERVATION%20OF%20NATIVE%20FLORA%20OF%20FLORIDA&ID=5B-40.0055),
The Integrated Taxonomic Information System (2011, p. 1),
NatureServe (2013, https://explorer.natureserve.org/servlet/NatureServe?loadTemplate=tabular_report.wmt&paging=home&save=all&sourceTemplate=reviewMiddle.wmt),
The online Atlas of Florida Vascular Plants (Wunderlin and
Hansen 2008, (https://www.florida.plantatlas.usf.edu/Plant.aspx?id=1122),
The Flora of North America (https://www.efloras.org/florataxon.aspx?flora_id=1&taxon_id=233501316), and
The Florida Natural Areas Inventory (FNAI) (FNAI, 2013,
https://fnai.org/trackinglist.cfm).
In summary, there is consensus that Trichomanes punctatum ssp.
floridanum is a distinct taxon.
Currently there are two extant metapopulations (groups of spatially
separated populations) of this subspecies (Gann et al. 2002, pp. 552-
554), comprising four populations in Miami-Dade County and two in
Sumter County, separated by a distance of approximately 400 kilometers
(km) (249 miles (mi)). As noted by Small (1938, p. 50), the Sumter
metapopulation is a considerable distance from where T. p. ssp.
floridanum was first discovered (i.e., south Florida) and resides in a
climate and habitat unlike the Miami-Dade County metapopulation. These
differences are likely why Morton (1963, p. 90) suggested that the
previous determination of these two metapopulations be reviewed. In
March 2014, the Service contracted researchers from Florida Atlantic
University to determine if the two metapopulations were the same
subspecies. Samples were collected from both metapopulations for
genetic analysis. DNA was isolated from the samples, and sequencing was
completed on five samples from each metapopulation. Researchers found
no observable differences in the sequence between the five samples
collected from Miami-Dade County and the five samples from Sumter
County, indicating that both metapopulations are the same subspecies
(Hughes 2014, pp. 1-4).
Life History
The life cycle of ferns is not commonly understood (Possley 2014c,
pers. comm.). Information about the specific life cycle of T. p. ssp.
floridanum is also lacking. Like all ferns, this taxon has two life-
history stages, a gametophyte stage and a sporophyte stage, and only
the sporophyte form is recognizable in the wild, while the gametophyte
form is very cryptic (Possley 2013a, pers. comm.; van der Heiden 2013b,
pers. comm.). Therefore, all reported populations of Trichomanes
punctatum ssp. floridanum have been in the sporophyte stage.
Mature plants can reproduce sexually or asexually. The initial
stage, when a spore germinates, is referred to as the gametophyte
stage. The gametophyte contains separate sperm and egg-producing
structures. In the presence of water or moisture, sperm reach the eggs
for fertilization. Fertilized eggs, under the proper conditions,
develop into sporophytes. The sporophytes produce spores, which in turn
can germinate to produce new gametophytes (Nelson 2000, pp. 17-19).
Reproduction may also occur in one other way: By division, when
rhizomes (horizontal, underground plant stems capable of producing the
shoot and root-like structures of a new plant) break, forming clones of
the parent plant.
Although it has been suggested that plants sporulate (produce
spores) mostly in the spring and summer (Nauman 1986, p. 182), field
observations in Miami-Dade County have observed sporangia in the months
of February, March, May, August, October, and December. The plants are
likely fertile any time of year; however, during the dry season,
sporophytes have been observed to desiccate and probably do not produce
spores (Possley 2013d, pers. comm.). In Sumter County, sporangia have
been observed from April through September; however, researchers
suggest they are likely producing all year, with peaks in the wet
season (van der Heiden 2013c, pers. comm.). For Trichomanes punctatum
ssp. floridanum, specific reproductive and growth requirements, such as
moisture levels needed for each stage of its life history, plant
longevity, growth rates, recruitment rates, dispersal methods, and
genetic variation, are currently unknown.
Organizations such as the Institute for Regional Conservation (IRC)
and Fairchild Tropical Botanic Garden (Fairchild) are working together
to understand the biology and life history of Trichomanes punctatum
ssp. floridanum. In 2002, IRC and Fairchild collaborated with fern
culture experts from Marie Selby Botanical Gardens (MSBG) in Sarasota,
Florida, and tissue culture experts at the Lindner Center for
Conservation and Research on Endangered Wildlife (CREW) in Cincinnati,
Ohio (Gann et al. 2009, pp. 35-36). Currently, Fairchild maintains
fewer than five healthy clusters of T. p. ssp. floridanum from plants
obtained in local hammocks (tropical hardwood forests) that are
monitored by their organization. The success of this effort to grow
healthy T. p. ssp. floridanum has yet to be determined due to several
factors, including: Slow growth rates, the formation of unusual linear
fronds, the susceptibility to mold, and the lack of sporulation
(Possley et al. 2013, pp. 43-45). However, researchers at CREW
[[Page 60442]]
have recently developed a successful method to culture T. p. ssp.
floridanum in-vitro and cryopreserve (to preserve by freezing at low
temperatures) sporophytes (V. Pence, submitted; Pence and Charls 2006,
pp. 29-34). The new plants from CREW have recently been transferred to
MSBG, and plans are under way to establish T. p. ssp. floridanum onto
limestone rock, which could potentially be transferred to solution hole
(see description under ``Habitat'' section, below) walls for eventual
reintroduction to the wild (Holst 2014, pers. comm.).
It is important to note that the numerous efforts to cultivate
Trichomanes punctatum ssp. floridanum ex-situ for possible future
reintroduction have been only partially successful. Researchers have
not been able to propagate T. p. ssp. floridanum via sexual
reproduction. Although they have been able to maintain the subspecies
in cultivation in the greenhouse for several months at a time, and
temporarily establish rhizome growth onto limestone rock, the
propagated fern eventually declines or becomes overrun with mosses.
Even when there is vegetative growth, there is no sign of spore
production (Holst 2014, pers. comm.).
Habitat
In southeastern North America, Trichomanes ssp. are considered rare
because of their delicate nature and requirements for deeply sheltered
habitats with almost continuous high moisture and humidity (Farrar
1993, pp. 190-197; Zots and Buche 2000, p. 203), restricting them from
a more widespread pre-glaciation distribution. Trichomanes punctatum
ssp. floridanum is considered strongly hygrophilous (growing or adapted
to damp or wet conditions) and generally perceived as restricted to
constantly humid microhabitat (Kr[ouml]mer and Kessler 2006, p. 57). T.
p. ssp. floridanum occurs only in the United States in the State of
Florida. In Florida, T. p. ssp. floridanum is known to occur only in
Miami-Dade and Sumter Counties.
Both extant metapopulations occur in dense canopy habitats, with
shady conditions that may be obligatory due to the poikilohydric (i.e.,
possessing no mechanism to prevent desiccation) nature of some fern
species (Kr[ouml]mer and Kessler 2006, p. 57). The canopy directly
contributes to the surrounding humidity of an area. Dense canopies
found in rockland habitats can minimize temperature fluctuations by
reducing soil warming during the day and heat loss at night. In areas
with greater temperature variations, as in Sumter County, this
temperature minimization effect can help prevent frost damage to the
interior of the hammock (FNAI 2010, p. 25). Mesic conditions are
further maintained by the hammock's rounded canopy profile, which
deflects winds, limiting desiccation during dry periods and reducing
interior storm damage (FNAI 2010, p. 25). Changes in the canopy can
impact humidity and evaporation rates, as well as the amount of light
available to the understory.
In Miami-Dade County, Trichomanes punctatum ssp. floridanum is
generally epipetric (a plant that grows on rocks) or epiphytic (a plant
that grows non-parasitically upon another plant), typically growing in
rocky outcrops of rockland hammocks, in oolitic (composed of minute
rounded concretions resembling fish eggs) limestone solution holes (see
description below), and, occasionally, on tree roots in limestone-
surrounded areas (Phillips 1940, p. 166; Nauman 1986, p. 180; Whitney
et al. 2004, pp. 105-106; Possley 2013e, pers. comm.; van der Heiden
2014b, pers. comm.). These rockland habitats are outcrops primarily
comprising marine limestone representing the distinct geological
formation of the Miami Rock Ridge, a feature that encompasses a broad
area from Miami to Homestead, Florida, and narrows westward through the
Long Pine Key area of Everglades National Park (ENP) (Snyder et al.
1990, pp. 233-234). Several endemic plant species have been identified
to be closely associated with the rocklands of southern Florida; these
plants are believed to have no adaptation for long-distance dispersal,
suggesting a lengthy period of evolution on rocky substrate in southern
Florida (Snyder et al. 1990, p. 236).
Rockland hammocks are a type of rich tropical hardwood forest on
upland sites in areas where limestone is very near the surface and
often exposed. Once numerous throughout South Florida, these rockland
hammocks have a diverse closed canopy and shrub layer, where more than
120 native tree and shrub species are known to occur, including a
number of rare plant and animal species, federally listed and candidate
species, South Florida endemics, and tropical species at or near the
northern limit of their ranges (Phillips 1940, p. 166; Snyder et al.
1990, p. 16; Gann et al. 2009, p. 3). The forest floor is characterized
by leaf litter with varying amounts of exposed limestone and has few
herbaceous species. Rockland hammocks generally consist of larger,
mature trees in the interior, while the margins can be almost
impenetrable due to dense growth of smaller shrubs, trees, and vines
(FNAI 2010, pp. 24-27). The canopy cover is typically very dense where
Trichomanes punctatum ssp. floridanum occurs. In Miami-Dade County, the
hammocks consist of a mix of temperate and tropical hardwood trees,
both canopy and understory, including Ocotea coriacea (lancewood),
Coccoloba diversifolia (pigeon plum), Quercus virginiana (live oak),
Simarouba glauca (paradise tree), Ficus aurea (strangler fig), and
Sideroxylon foetidissimum (mastic) (see Snyder et al. 1990, p. 241, for
complete list). Soils where T. p. ssp. floridanum is extant in Miami-
Dade County generally consist of an uneven layer of highly organic soil
overlying rock (Snyder et al. 1990, p. 238); soils are classified as
Matecumbe Muck (moderately well-drained soils that are very shallow)
(Florida Geographic Data Library 2013, https://www.fgdl.org/). Soils
from historical and extant records consist of the following soil types:
Krome Very Gravelly Loam, Cardsound Silty Clay Loam-Rock Outcrop
Complex, Opalocka Sand-Rock Outcrop Complex, and Dania Muck.
The limestone solution holes are considered specialized habitat
within these hammock areas that host Trichomanes punctatum ssp.
floridanum, as well as several other fern species (Snyder et al. 1990,
p. 247). The solution hole features that dominate the rock surface in
the Miami Rock Ridge are steep-sided pits, varying in size, formed by
dissolution of subsurface limestone followed by a collapse above
(Snyder et al. 1990, p. 236). Limestone solution holes vary in size,
from shallow holes less than 0.5 meter (m) (1.6 feet (ft)) deep to
those that cover over 100 m\2\ (1,076 ft\2\) and are several meters
deep (Snyder et al. 1990, p. 238). The bottoms of most solution holes
are filled with organic soils, while deeper solution holes penetrate
the water table and have (at least historically) standing water for
part of the year (Snyder et al. 1990, pp. 236-238). Humidity levels are
higher in and around the solution holes because of standing water and
moisture retained in the organic soils. Many tropical, epipetric plant
species are associated with the sinkholes and solution holes in
rockland hammocks.
In Sumter County, Trichomanes punctatum ssp. floridanum is known to
be epipetric, residing on limestone boulders in high atmospheric
humidity hammocks (van der Heiden 2013a, pers. comm). The extant
populations are located in mesic hammocks on limestone boulders 0.1-1.5
m (0.3-4.9 ft) tall (see ``Current Range'' section,
[[Page 60443]]
below). Mesic hammock is a developed evergreen hardwood and/or palm
forest on soils that are rarely inundated (FNAI 2010, pp. 19-23) and
commonly associated with hydric hammock and mixed wetland hardwoods.
The difference between mesic hammocks and surrounding habitats is a
slight difference in elevation. Mesic hammocks occur on higher ground
within basin or floodplain wetlands; as patches of oak/palm forest in
dry prairie or flatwoods communities; on river levees; in ecotones
(transition area between two biomes or areas of distinct plant and
animal groups) between wetlands and upland communities; and at the
edges of lakes, sinkholes, other depressional or basin wetlands, and
river floodplains where natural fires do not occur (FNAI 2010, pp. 19-
23).
Recent field surveys (van der Heiden 2015a, p. 6; van der Heiden
2015b, unpublished data; van der Heiden 2015c, unpublished data) have
provided additional information regarding potential suitable habitat in
Sumter County. These surveys, conducted by IRC and funded by the
Service, delineated suitable habitat within and around the Jumper Creek
Tract of the Withlacoochee State Forest. Within surveyed areas, IRC
mapped all suitable substrate found in areas having suitable canopy and
hydrology to support growth of Trichomanes punctatum ssp. floridanum.
The resulting map included limestone rocks and boulders in not only
mesic hammock, but also hydric hammock, elevated hydric hammock, and
(in a small number of instances) adjacent wetland (but non-hammock)
habitats. The Service is still evaluating this information and working
with IRC to further refine suitable habitat parameters for the fern in
Sumter County. Despite extensive surveys through approximately 1,904 ha
(4,705 ac) in and around the Jumper Creek Tract, van der Heiden (2015a,
p. 9) did not find any new populations of T. p. ssp. floridanum.
Although there are several occurrences of Trichomanes punctatum
ssp. floridanum in Sumter County where sunlight can be observed through
the canopy, generally the habitat is shaded throughout the year, with
the lowest amount of canopy cover recorded at approximately 65 percent
(van der Heiden and Johnson 2014, p. 20; in Rocky Hammock). T. p. ssp.
floridanum has been observed growing on small limestone rocks, as well
as boulders with tall, horizontal faces with numerous other species,
including rare State-listed species (e.g., Asplenium cristatum (hemlock
spleenwort)) and widespread Pecluma dispersa (widespread polypody) (van
der Heiden 2013b, pers. comm.; van der Heiden and Johnson 2014, pp. 15-
16).
Within one occupied Sumter County hammock (Rocky Hammock), the
majority of Trichomanes punctatum ssp. floridanum occur on the northern
face of limestone boulders; however, those clusters found on non-north-
facing limestone generally occur in close proximity to other boulders,
trees, or within protected crevices (van der Heiden and Johnson 2014,
p. 7). Van der Heiden and Johnson (2014, pp. 9-10) suggested that the
northern aspect of limestone boulders is more often inhabited by this
taxon because of the reduced exposure to sunlight, promoting cooler
temperatures and higher moisture as compared to other sun-exposed
sections of rock. This may also be the case for those clusters shielded
by other boulders, by trees, or in crevices, allowing the plant to grow
on any portion of the shielded rock as long as moisture levels remain
high enough to prevent desiccation (van der Heiden and Johnson 2014,
pp. 9-10). Additionally, both populations of T. p. ssp. floridanum in
Sumter County grow within the northern quadrant of each hammock.
Soils of mesic hammock are sands mixed with organic matter, often
containing a thick layer of leaf litter and generally well-drained.
Although some areas maintain high-moisture soils due to the
accumulation of leaf litter and extensive canopy cover, in general,
mesic hammocks can occur across a broad gradient of soil moisture
conditions, from somewhat xeric to almost hydric soils. Rock outcrops
may also occur in mesic hammocks, especially where limestone is near
the surface (FNAI 2010, pp. 19-23). Soil types for the extant
metapopulation of Trichomanes punctatum ssp. floridanum in Sumter
County include Okeelanta Muck, Frequently Flooded, and Mabel Fine Sand
(i.e., deep and very deep, somewhat poorly drained, slowly permeable
soils that formed in sandy to clayey marine deposits, with a bouldery
(abounding in rocks or stones) subsurface and 0-5 percent slopes
(Florida Geographic Data Library 2013, https://www.fgdl.org/)).
Additionally, one historical record has Adamsville Fine Sand, Bouldery
Subsurface, while another population containing a questionable record
from an extirpated population has what is classified as Malabar Fine
Sand, Frequently Flooded.
Plant communities associated with mesic hammocks vary depending on
the latitude; tropical species gradually increase in frequency from the
central to southern peninsular Florida. In south Florida, some high-
elevation areas dry enough to support a semi-tropical mesic hammock do
exist; however, most ``high hammocks'' are rockland hammocks occurring
on limestone (FNAI 2010, pp. 19-23). Q. virginiana is common in mesic
hammock communities. Oak species found in these hammocks tend to
possess a broader tolerance of a range of conditions than do oaks in
other habitats (FNAI 2010, pp. 19-23). Mesic hammocks do not contain
wetland trees, as found in hydric hammocks; however, these two hammock
types often occur as intermixed stands. Because mesic hammocks are
often associated with hydric hammocks, with wetlands, or as a
transition to uplands, they are sensitive to hydrologic alteration in
the landscape. For example, changes in flooding frequency and/or
duration can kill most mesic hammock tree species, while lowered water
tables can shift vegetation towards xeric species or promote wildfires,
destroying the hammock (FNAI 2010, pp. 19-23). Mesic hammocks may be
distinguished from rockland hammocks by the dominance of temperate
species in the canopy, whereas rockland hammocks are composed of
predominantly tropical woody species.
Trichomanes punctatum ssp. floridanum in Sumter County can be found
under a dense canopy including Q. virginiana, Sabal palmetto (cabbage
palm), Carpinus caroliniana (American hornbeam), Celtis laevigata
(sugarberry), Acer negundo (boxelder), Liquidambar styraciflua
(sweetgum), and Sapindus saponaria (wingleaf soapberry) (van der Heiden
2013c, pers. comm.; van der Heiden and Johnson 2014, p. 19). The
hammocks where T. p. ssp. floridanum has been found are also surrounded
by a mosaic of wetlands dominated by Taxodium distichum (cypress
trees). Field surveys of Sumter County populations recorded 18 canopy
species in Rocky Hammock and 12 in Tree Frog Hammock (van der Heiden
and Johnson 2014, p. 19). The average canopy closure for both
populations in Sumter County has been estimated to be more than 75
percent, where it is heavily shaded, maintaining high humidity to
reduce chances of desiccation (van der Heiden and Johnson 2014, p. 9).
Van der Heiden and Johnson (2014, p. 9) speculate this dense, closed
canopy can serve as a shield for T. p. ssp. floridanum to inhibit the
growth of other plant species on the same part of an inhabited rock
area.
Although it is believed this subspecies needs high temperatures
(although likely not above 100 degrees Fahrenheit ([deg]F); Possley
2014c, pers. comm.) and humidity, along with dense
[[Page 60444]]
canopy, there is limited information on optimal temperature and
humidity ranges or thresholds for Trichomanes punctatum ssp. floridanum
growth and survival. In Miami-Dade County where T. p. ssp. floridanum
currently is found, the mean maximum temperature from 2004 to 2013 was
29.0 degrees Celsius ([deg]C) (84.3[emsp14][deg]F), and the mean
minimum temperature for the same time period was 21.4 [deg]C
(70.5[emsp14][deg]F) (https://www1.ncdc.noaa.gov). In contrast, yearly
mean temperatures were lower for Sumter County with 23.4 [deg]C
(74.2[emsp14][deg]F) recorded as the mean maximum temperature from 2004
to 2013, and 11.8 [deg]C (53.2[emsp14][deg]F) as the mean minimum
temperature for the same time period (National Oceanic and Atmospheric
Administration 2014, https://www1.ncdc.noaa.gov).
Recent field studies have provided some data on microhabitat
conditions (e.g., temperature and humidity) for Trichomanes punctatum
ssp. floridanum populations in Sumter County. Van der Heiden and
Johnson (2014, pp. 8, 21) found average relative humidity to be around
95 percent in both Rocky Hammock and Tree Frog Hammock, while average
ambient temperature in both hammocks was approximately 21 [deg]C
(70[emsp14][deg]F) from September 2013 to November 2013. However,
during cooler periods (19-21 [deg]C; 66-70[emsp14][deg]F) when humidity
levels dropped slightly (by approximately 2 percent), observed plant
health declined, demonstrating the fragile nature of this taxon and its
dependence on high-humidity conditions (van der Heiden and Johnson
2014, pp. 9, 21). Collection of humidity and temperature data within
these same areas was subsequently continued through March 2015. From
September 2013 to March 2015, average monthly temperatures in both
hammocks were very similar and ranged from approximately 12 [deg]C
(53[emsp14][deg]F; in January 2014) to 25 [deg]C (78[emsp14][deg]F; in
August 2014) (van der Heiden 2015a, p. 17). The average relative
humidity in both hammocks was 94.8 percent throughout the study (van
der Heiden 2015a, p. 5). This type of information needs to be further
explored to determine habitat requirements (i.e., thresholds for
humidity and temperature) for both metapopulations of this taxon.
Historical Range/Distribution
The historical range of Trichomanes punctatum ssp. floridanum
included southern (Miami-Dade County; see Table 1, below) and central
(Sumter County; see Table 2, below) Florida.
Miami-Dade County
In Miami-Dade County, the historical range of this subspecies
extended from its southern limit in Royal Palm Hammock (now part of
ENP) northeast to Deering-Snapper Creek Hammock, which includes the
modern-day site of Smather's Four Fillies Farm residential area, near
R. Hardy Matheson Preserve (derived from Gann et al. 2002, pp. 552-
554), a range of at least 45 square kilometers (km\2\) (17 square miles
(mi\2\)). Plants in Miami-Dade were known to historically occur in at
least 11 hammocks: Deering-Snapper Creek Hammock, Castellow Hammock,
Silver Palm Hammock (also known as Caldwell), Ross Hammock, Royal Palm
Hammock (in ENP), Hattie Bauer Hammock, Shields Hammock, Nixon-Lewis
Hammock, Fuchs Hammock, Addison Hammock (in the Deering Estate at
Cutler), and Matheson Hammock. In the 1980s, T. p. ssp. floridanum was
also documented in Meissner Hammock and Cox Hammock (now part of the
tourist attraction ``Monkey Jungle'') (Small 1918, p. 6; Small 1921, p.
211; Morton 1963 p. 90; Fairchild Tropical Garden 1968, p. 1; Nauman
1986 p. 182; Gann et al. 2002, pp. 552-554; Gann 2013, https://regionalconservation.org/ircs/database/plants/IRCSpAccount.asp?TXCODE=Tricpuncflor&GENUS=Trichomanes&SPECIES=punctatum&Author=Poir.&INFRA1=subsp.&INFRA1NAME= ssp.
floridanum&INFRA1AUTHOR=Wess.%20Boer&CommonNames=Florida%20bristle%20fer
n).
J.K. Small documented Trichomanes punctatum ssp. floridanum in 1901
at Deering-Snapper Creek. J.K. Small made subsequent collections of the
subspecies in and around Miami-Dade County including one in 1903,
probably located in or near present-day Castellow Hammock (Gann 2014d,
pers. comm.). A.A. Eaton collected additional specimens from Castellow
Hammock in 1903. More recent observations of T. p. ssp. floridanum in
Castellow Hammock include documentation by G. Gann and K. Bradley in
the late 1990s (Bradley and Gann 1999), and subsequent observations by
J. Possley and others (Gann et al. 2002, pp. 552-554; Possley et al.
2013, pp. 43-45). T. p. ssp. floridanum was collected by A.A. Eaton in
Silver Palm Hammock in 1903 and reported again in 1980; however, the
1980 report was not confirmed. The fern was collected from Ross Hammock
by J.K. Small and colleagues in 1906. Since then, part of this hammock
has been damaged, and what remains is currently protected as a Miami-
Dade County Environmentally Endangered Lands (EEL) Preserve. In 1909,
the subspecies was collected in Royal Palm Hammock (also known as
Paradise Key), now within ENP, and later reported by W.E. Stafford in
1917 (Stafford 1919, p. 386; Gann et al. 2002, pp. 552-554).
Several collections of Trichomanes punctatum ssp. floridanum were
made in Miami-Dade in 1915, including: Hattie Bauer Hammock, Shields
Hammock, Nixon-Lewis Hammock, Fuchs Hammock, and Deering-Snapper Creek
Hammock. Hattie Bauer Hammock, now a Miami-Dade County conservation
area, has numerous subsequent collection records by Small (1915, 1916),
Correll (1936), and McFarlin (1934, 1940) as cited by Gann 2013, https://regionalconservation.org/ircs/database/plants/IRCSpAccount.asp?TXCODE=Tricpuncflor&GENUS=Trichomanes&SPECIES=punctatum&Author=Poir.&INFRA1=subsp.&INFRA1NAME= ssp.
floridanum&INFRA1AUTHOR=Wess.%20Boer&CommonNames=Florida%20bristle%20fer
n. The last known collection in Hattie Bauer Hammock was recorded in
1960, by T. Darling, Jr. It was subsequently reported as extirpated by
Gann et al. (2002, pp. 552-554), until it was rediscovered in this
hammock in 2011 by Possley (Possley et al. 2013, pp. 1-2). Shields
Hammock was destroyed prior to 1991 (Cressler 1991, Handwritten Notes).
Fuchs Hammock is now part of the Fuchs Hammock Preserve (Gann et al.
2002, pp. 552-554), and the subspecies was vouchered (pressed plant
samples taken for future reference) again in 1954, by L. J. Brass; in
1959, by T. Darling Jr.; and in 1969, by F.C. Craighead (The Institute
for Regional Conservation, Herbarium Specimens, Floristic Inventory of
South Florida Database, September 12, 2007). T. p. ssp. floridanum was
also vouchered in Fuchs Hammock in 1993, following Hurricane Andrew
(1992) by A. Cressler (Cressler 12 February 1993, handwritten notes),
and it has been more recently observed by Possley and others over the
years (Gann et al. 2002, pp. 552-554; Possley et al. 2013, pp. 43-45).
T. p. ssp. floridanum was observed by G. N. Avery in 1983 in Meissner
Hammock (immediately adjacent to Fuchs Hammock) and was since vouchered
by K. Bradley in 1997 and 2002 and also observed by others (Gann et al.
2002, pp. 552-554; Possley et al. 2013, pp. 43-45).
In 1916, J.K. Small reported Trichomanes punctatum ssp. floridanum
in Addison Hammock, now located within Deering Estate at Cutler,
[[Page 60445]]
currently Miami-Dade County Park; however, these reports were never
vouchered (J.K. Small 1916; Gann et al. 2002, pp. 552-554). Surveys in
recent years have yet to find any populations of T. p. ssp. floridanum
in Deering Estate at Cutler, Matheson Hammock, or Silver Palm Hammock
(Possley 2013i, pers. comm.). The subspecies was last reported from Cox
Hammock in 1989, by A. Cressler, where plants were observed in a
sinkhole in the tourist attraction ``Monkey Jungle'' (Cressler 1991,
handwritten notes); it is not known if these plants still exist. Cox
Hammock is located about 1.6 km (1.0 mi) northeast of Castellow Hammock
Park. Additional hammocks existing today where the taxon formerly
occurred include Ross and Royal Palm Hammock (in ENP) and Deering-
Snapper Creek Hammock. A section of Deering-Snapper Creek Hammock was
destroyed in 1912-1913, when the Snapper Creek Canal was constructed.
Dredging of this canal drastically altered the water table in the area,
depleting the freshwater springs, while a large spoil berm from
excavation of the canal destroyed habitat (Metro-Dade County Park and
Recreation Department 1991, p. 10). Other hammocks in the historical
range that are presumed destroyed include Nixon Lewis Hammock, which is
partially destroyed (Gann 2013, https://regionalconservation.org/ircs/database/plants/IRCSpAccount.asp?TXCODE=Tricpuncflor&GENUS=Trichomanes&SPECIES=punctatum&Author=Poir.&INFRA1=subsp.&INFRA1NAME= ssp.
floridanum&INFRA1AUTHOR=Wess.%20Boer&CommonNames=Florida%20bristle%20fer
n) and a station presumably near the Matheson Hammock Park vouchered by
G. Peterson in 1940.
Table 1--Summary of Historical Reports and Current Population and Hammock Status of Each Trichomanes Punctatum ssp. Floridanum Location in Miami-Dade
County
[Gann et al. 2002; The Institute for Regional Conservation, Herbarium Specimens, Floristic Inventory of South Florida Database, September 12, 2007;
Florida Natural Areas Inventory element occurrences 9/12/2013; Possley 2013c, i-j, 2014a-c; Possley 2013, 2014a pers. comm.; Gann 2013, pers. comm.; van
der Heiden 2013e, pers. comm.; Gann 2014a-f, pers. comm.; Gann et al. 2001-2014). Population locations (hammocks) are numbered in chronological order by
T. p. ssp. floridanum initial discovery date.]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Year(s) of Number of
No. Population location initial Observer specimens Current population Current hammock status
report(s) collected status
--------------------------------------------------------------------------------------------------------------------------------------------------------
1....................... Deering-Snapper Creek 1901 J.K. Small, G.V. Nash. 3 Extirpated............ Protected Area,
Hammock-Smather's Partially Destroyed.
Four Fillies Farm (R.
Hardy Matheson
Preserve).
1915 J.K. Small, C.A. 1
Mosier.
2....................... Castellow Hammock..... 1903 J.K. Small, J.J. 2 Extant................ Protected Area.
Carter.
1903 A.A. Eaton............ 4
3....................... Silver Palm Hammock... 1903 A.A. Eaton............ 1 Extirpated............ Protected Area.
4....................... Ross Hammock.......... 1906 J.K. Small, J.J. 2 Extirpated............ Protected Area,
Carter. Partially Destroyed.
5....................... Royal Palm Hammock 1909 J.K. Small, J.J. 2 Extirpated............ Protected Area.
(ENP); aka Paradise Carter.
Key.
1917 W.E. Stafford......... None
1915 J.K. Small, C.A. 2
Mosier.
1915 J.K. Small............ 3
1915 J.K. Small, C.A. 5
Mosier, G.K. Small.
6....................... Hattie Bauer Hammock 1916 J.K. Small............ 1 Extant................ Protected Area.
(Orchid Jungle).
1934 J.B. McFarlin......... 2
1936 D.S. Correll.......... 2
1940 J.B. McFarlin......... 1
1960 T. Darling Jr......... 1
7....................... Shields Hammock....... 1915 J.K. Small, C.A. 1 Extirpated............ Destroyed.
Mosier, G.K. Small.
8....................... Nixon-Lewis Hammock... 1915 J.K. Small, C.A. 1 Extirpated............ Protected Area,
Mosier. Partially Destroyed.
9....................... Fuchs Hammock (Sykes 1915 J.K. Small, C.A. 1 Extant................ Protected Area.
Hammock). Mosier.
1954 L.J. Brass............ 1
1959 T. Darling Jr......... 1
1969 A.F. Clewell, F.C. 1
Craighead.
10...................... Deering Estate at 1916 J.K. Small............ None Unconfirmed \1\....... Protected Area.
Cutler (Addison
Hammock).
11...................... Matheson Hammock Park. 1940 G. Peterson........... 2 Unconfirmed \2\....... Protected Area.
12...................... Meissner Hammock...... 1983 G.N. Avery............ None Extant................ Protected Area.
13...................... Monkey Jungle (Cox 1989 A. Cressler........... None Unknown \3\........... Privately Owned,
Hammock). Partially Destroyed.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ Initial report is questionable.
\2\ Precise location of sample and associated report is questionable.
\3\ It is not known whether the subspecies still occurs here.
[[Page 60446]]
Sumter County
In Sumter County, early collections and herbarium label data for
Trichomanes punctatum ssp. floridanum are not accurate or precise in
their location descriptions. The first documented collection in 1936,
by R.P. St. John, simply states that T. p. ssp. floridanum was found
11.26 km (7.0 mi) east of Floral City. This collection is close to the
extant populations in Sumter (in Rocky Hammock within Withlacoochee
State Forest), which is east-southeast of Floral City, and is thought
to be the location where T. p. ssp. floridanum existed on private land
until it was cleared for cattle sometime after 1983. A specimen found 3
years later, by J.B. McFarlin in 1939, was originally thought to be T.
sphenoides; the herbarium label data described this collection as
``South of Floral City, Florida. T. sphenoides is a misapplied synonym
for T. p. ssp. floridanum according to FNAI. This is the only known
station in the United States.'' It is believed that these label data
may have been incorrectly recorded, indicating a direction of south
from Floral City, when it should have been east. In all likelihood,
McFarlin's collection probably referred to the population in the Wahoo
area, where St. John previously collected because he states his
collection was from the same locality where it was originally found in
1936. The specimen found by McFarlin eventually led to reports of the
taxon in Citrus County (Wherry 1964, p. 232; Nelson 2000, p. 81);
however, this was never confirmed beyond the initial report. Systematic
surveys have not been conducted in Citrus County; therefore, the only
documented occurrences of T. p. ssp. floridanum in this region of
Florida have been in Sumter County, just north of Wahoo and east of the
Withlacoochee River.
Several years later, in 1954, R. Garrett collected Trichomanes
punctatum ssp. floridanum southeast of Floral City. It is thought to be
the same location where St. John and McFarlin made their previous
collections; however, label data were again minimal and the exact
location is uncertain. In 1959, T. Darling Jr. found this subspecies
near Floral City, 11.26 km (7.0 mi) south near a location called Battle
Slough. This record has never been confirmed because it is located on
private property. Another specimen was found in 1963, by O. Lakela in
an area known as Indian Field Ledges. Lakela recorded his location and
collection to be west of Withlacoochee River off State Road #48. This
information is believed to be incorrect based on a site visit by
Darling (1961, p. 7), stating that the Indian Field Ledges is north of
Wahoo, a locality east of the Withlacoochee River. T. p. ssp.
floridanum was not found again in Sumter County until 1983, when SW.
Leonard made a collection on private property known as Rocky Point,
north of Wahoo. This is presumed to be the same location where St.
John, McFarlin, and Garrett collected their specimens. This population
is now extirpated.
Table 2--Summary of Presumed Extirpated, Extirpated, and Unconfirmed Trichomanes Punctatum ssp. Floridanum Populations in Sumter County
[Gann et al. 2002; The Institute for Regional Conservation, Herbarium Specimens, Floristic Inventory of South Florida Database, September 12, 2007;
Florida Natural Areas Inventory Element Occurrences 9/12/2013; van der Heiden 2013d, 2014a, pers. comm.; Gann et al. 2001-2014). Population locations
(hammocks) are numbered in chronological order by T. p. ssp. floridanum initial discovery date.]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
No. Population location Year of Observer specimens Current population Current hammock
initial report collected status status
--------------------------------------------------------------------------------------------------------------------------------------------------------
1................................. 11.26 km (7 mi) East 1936 R.P. St. John....... 1 Presumed Extirpated. Privately Owned,
of Floral City \1\. Presumed Destroyed.
2................................. Floral City Area \1\. 1939 J.B. McFarlin....... 1 Unconfirmed \2\..... Unknown.
3................................. Southeast of Floral 1954 R. Garret........... 1 Presumed Extirpated. Privately Owned,
City \1\. Presumed Destroyed.
4................................. Floral City, 11.26 km 1959 T. Darling Jr....... 1 Unconfirmed \2\..... Privately Owned,
(7 mi) south (Battle Unknown.
Slough) \1\.
5................................. East of Withlacoochee 1963 O. Lakela........... 1 Extirpated.......... Protected Area.
River, off State
Road #48 (Indian
Field Ledges) \1\.
6................................. Rocky Point, (north 1983 S.W. Leonard........ 1 Extirpated.......... Privately Owned,
of Wahoo). Destroyed.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ Sumter County collections and herbarium label data for Trichomanes punctatum ssp. floridanum are inaccurate in location descriptions.
\2\ Initial report is questionable.
Current Range
The extant metapopulation of Trichomanes punctatum ssp. floridanum
in Miami-Dade County is approximately 400 km (249 mi) south of the
extant metapopulation in Sumter County. Both metapopulations of T. p.
ssp. floridanum are located entirely on public lands (see Table 3,
below). In general, Trichomanes punctatum ssp. floridanum occurs in
small areas within each hammock.
Table 3--Summary of Known Extant Occurrences of Trichomanes punctatum ssp. floridanum.
[Possley 2013, pp. 1-2; Dozier 2014, Pers. Comm.; van der Heiden and Johnson 2014, pp. 5, 26]
----------------------------------------------------------------------------------------------------------------
Number of
Metapopulation location (county) Population location Land ownership subpopulations Status
----------------------------------------------------------------------------------------------------------------
Miami-Dade...................... Meissner Hammock....... State............. 2 Extant.
Miami-Dade...................... Fuchs Hammock Preserve. County............ 4 Extant.
Miami-Dade...................... Castellow Hammock Park. County............ 3 Extant.
[[Page 60447]]
Miami-Dade...................... Hattie Bauer Hammock... County............ 1 Extant.
Sumter.......................... Rocky Hammock, State............. 1 Extant.
Withlacoochee State
Forest's Jumper Creek
Tract.
Sumter.......................... Tree Frog Hammock, State............. 1 Extant.
Withlacoochee State
Forest's Jumper Creek
Tract.
----------------------------------------------------------------------------------------------------------------
Miami-Dade County
The four populations that constitute the Miami-Dade County
metapopulation are located in urban preserves managed by the County's
EEL Program and the Natural Areas Management (NAM) Division of Miami-
Dade County's Parks, Recreation and Open Spaces (PROS) Department (see
Factor A, Conservation Efforts to Reduce Habitat Destruction,
Modification, or Curtailment of Its Range, below). These EEL Preserves
include: Castellow Hammock Park (39.5 hectares (ha)) (97.6 acres (ac)),
Hattie Bauer Hammock (5.7 ha (14.0 ac)), Fuchs Hammock Preserve (15.7
ha (38.8 ac)), and Meissner Hammock (4.1 ha (10.1 ac)). Three of these
preserves (76 percent of the land area) are owned by the County; the
fourth, Meissner Hammock (24 percent), is owned by the State and leased
to the County (Dozier 2014, pers. comm.). The population in Fuchs
Hammock Preserve includes a new subpopulation that was found in July
2013 (Possley et al. 2013, pp. 43-45). Fuchs and Meissner Hammocks are
immediately adjacent to each other, and Castellow Hammock Park is 10.5
km (6.5 mi) to the northeast. Although the fern was thought to be
extirpated from Hattie Bauer Hammock in 1960, another population was
re-discovered there in 2011 (8 ha (20 ac)) (Possley et al. 2013, pp.
43-45). Hattie Bauer Hammock is 4.02 km (2.5 mi) south of Castellow
Hammock and approximately 8.05 km (5 mi) northeast of Fuchs and
Meissner Hammocks.
No comprehensive survey has been conducted in rockland hammocks in
Miami-Dade County where suitable Trichomanes punctatum ssp. floridanum
habitat has been identified. Although these areas have been extensively
explored by numerous botanists and plant enthusiasts, including sites
where the subspecies was formerly found, due to the cryptic nature of
this plant it may have been overlooked and new occurrences may yet be
discovered (Possley 2013e, pers. comm.; van der Heiden 2013c, pers.
comm.). Surveys conducted in the late 1990s, and as late as 2010, did
not find T. p. ssp. floridanum in Silver Palm Hammock (Gann et al.
2002, pp. 552-554; Possley 2013f, pers. comm.). A sporophyte sample was
collected in Nixon-Lewis Hammock by Small and Mosier in 1915; however,
due to extensive disturbance of this hammock, subsequent surveys
conducted in 2006, by IRC, could not find the taxon (Bradley and Gann
2005, unpublished data). Over the years, IRC has completed systematic
surveys in ENP in Royal Palm Hammock and other hammocks on Long Pine
Key (also in ENP); however, sporophytes have not been found there (Gann
et al. 2009; pp. 1-66). In 2003, based on historical records, staff
from ENP and IRC surveyed Royal Palm Hammock for T. p. ssp. floridanum
without success; subsequent surveys conducted in rockland hammocks
throughout Long Pine Key for other rare plants also were not successful
in finding T. p. ssp. floridanum (Sadle 2013, pers. comm.).
Sumter County
The Sumter County metapopulation consists of two extant populations
of Trichomanes punctatum ssp. floridanum that have been reported north
of Wahoo, in the Withlacoochee State Forest's Jumper Creek Tract; these
populations are located in Rocky Hammock (located on 44 boulders) and
Tree Frog Hammock (located on 4 boulders) (van der Heiden and Johnson
2014, p. 7). The population in Tree Frog Hammock was discovered as
recently as April 2013, during regional surveys (van der Heiden 2013c,
pers. comm.). Two additional populations were known from private land
just south of the State Forest; however, these populations were
subsequently extirpated due to the clearing of land for agriculture by
the property owner (van der Heiden 2013c, pers. comm.).
Recent GIS analyses show the soil type associated with known extant
occurrences of Trichomanes punctatum ssp. floridanum in the northern
metapopulation to be Okeelanta Muck, Frequently Flooded; this soil
covers approximately 1,478 ha (3,652 ac) in Sumter County. However, not
all of these areas have been systematically surveyed. Surveys were
conducted of a boulder field within Withlacoochee State Forest's Jumper
Creek Tract (called the Indian Field Ledges) in August 2007 and April
2013 and were unsuccessful (van der Heiden 2013c, pers. comm.). The
discovery of new populations may be possible in the area. Indeed, the
population of this subspecies in Jumper Creek's Tree Frog Hammock is a
new population that was discovered in April 2013, during additional
hammock surveys within Withlacoochee State Forest and the surrounding
area (van der Heiden 2013c, pers. comm.). However, IRC recently
conducted extensive surveys through approximately 1,904 ha (4,705 ac)
in and around the Jumper Creek Tract, and no additional populations of
T. p. ssp. floridanum were located (van der Heiden 2015a, p. 9).
It is also possible that other subpopulations may exist in Sumter
County. Indian Ledges, a hammock located on private land near Jumper
Creek (not to be confused with Indian Field Ledges), just north of
Wahoo, is believed to be suitable for Trichomanes punctatum ssp.
floridanum, including a dense canopy and appropriate soil (Deangelis
2014a-b, pers. comm.). Over the years, many rare ferns and orchids have
been observed in the Indian Ledges Hammock; unfortunately, this hammock
was heavily damaged by hurricanes in 2004 (Deangelis 2014a, pers.
comm.).
Portions of the Southwest Florida Water Management District
(SWFWMD) property within the Green Swamp, more than 40.23 km (25 miles)
southeast of the Jumper Creek Tract in Withlacoochee State Forest, may
also contain appropriate habitat for Trichomanes punctatum ssp.
floridanum based on existing habitat features such as dense canopy,
high humidity microclimates, mesic hammock, and limestone outcroppings
(Elliott 2014, pers. comm.). The SWFWMD property within the Green Swamp
is the only area where land alteration has not occurred in Sumter
[[Page 60448]]
County (11,343 ha (28,030 ac)). Portions of Green Swamp owned by the
SWFWMD also extend into three other counties: Lake, Polk, and Pasco.
Future survey efforts, coordinating with local land owners and
conservation organizations in this area, may prove successful in
finding new populations of T. p. ssp. floridanum.
Population Estimates and Status
Trichomanes punctatum ssp. floridanum grows in dense mats and is
rhizomatous (a horizontal stem that often sends out root-like
structures from its nodes). Fronds are scattered in matted clusters
along the stems, making it difficult to count clusters, or groups of
plants in the same location, and nearly impossible to accurately count
individual plants (Nelson 2000, p. 79). This issue has been encountered
in other Trichomanes species, such as Trichomanes boschianum
(Appalachian bristle fern) (Hill 2003, p. 11). As such, populations are
typically described by the number of clusters (i.e., groups of plants
in various sinkholes, on tree roots, on boulders) and the total area
covered by the cluster.
Miami-Dade County
In Miami-Dade County, there are four populations of the fern with a
total of 10 subpopulations (i.e., nine solution holes and one rocky
outcropping on a tree root). Overall, this taxon occurs in small areas
(i.e., less than 0.5 ha (1.2 ac)) at each site, with 88 percent of the
total area in three subpopulations in Castellow Hammock. Recent surveys
(see Table 4, below) in Miami-Dade by Fairchild (Possley 2013, pp. 1-2)
found the fern covering a total area of approximately 9.92 m\2\ (106.56
ft\2\) (Possley 2013, pp. 1-2).
Table 4--Area Covered by Each of 10 Known Subpopulations of Trichomanes punctatum ssp. floridanum in Miami-Dade
County, October and November 2013
[(Possley 2013, pp. 1-2) and in Sumter County, December 2013 (van der Heiden and Johnson 2014, pp. 7, 14)]
----------------------------------------------------------------------------------------------------------------
Estimated area Number of
Metapopulation Population Subpopulation covered (m\2\) clusters
----------------------------------------------------------------------------------------------------------------
Miami-Dade....................... Hattie Bauer Hammock Hole (no tag)...... 0.078 2-10
Miami-Dade....................... Fuchs Hammock....... Hole 532........... 0.017 2-10
Miami-Dade....................... Fuchs Hammock....... Hole 533........... 0.038 2-10
Miami-Dade....................... Fuchs Hammock....... Hole 1431.......... 0.128 2-10
Miami-Dade....................... Fuchs Hammock....... Root 1430.......... 0.047 1
Miami-Dade....................... Meissner Hammock.... Hole 2319.......... 0.145 2-10
Miami-Dade....................... Meissner Hammock.... Hole 3337.......... 0.713 2-10
Miami-Dade....................... Castellow Hammock... Hole 2332.......... 4.688 11-100
Miami-Dade....................... Castellow Hammock... Hole 2331.......... 3.925 11-100
Miami-Dade....................... Castellow Hammock... Hole 944........... 0.141 2-10
-----------------------------------
Miami-Dade County Total...... .................... ................... 9.920 ..............
Sumter........................... Rocky Hammock....... N/A................ 4.355 44
Sumter........................... Tree Frog Hammock... N/A................ 0.132 4
-----------------------------------
Sumter County Total.......... .................... ................... 4.487 ..............
------------------------------------------------------------------------------
TOTAL Area Covered........... .................... ................... 14.407 ..............
----------------------------------------------------------------------------------------------------------------
The largest known population of Trichomanes punctatum ssp.
floridanum in Miami-Dade County is located at Castellow Hammock
(Possley et al. 2013, p. 43), where it occurs in three of the larger
subpopulations. In October of 2011, field surveys revealed extensive
desiccation of this population after intensive nonnative vegetation
removal (Possley 2013g, pers. comm.); however, by November 2013, these
plants had recovered, and the total area covered by all clusters (i.e.,
two or more plants next to each other) was estimated at 8.754 m\2\
(94.227 ft\2\). Meissner Hammock has two subpopulations; the clusters
in this hammock cover an area of 0.858 m\2\ (9.235 ft\2\) and are
considered healthy, with no signs of desiccation (Possley et al. 2013,
pp. 43-45). There is one subpopulation in Hattie Bauer Hammock covering
approximately 0.78 m\2\ (8.4 ft\2\), and three subpopulations of T. p.
ssp. floridanum at Fuchs Hammock, with an additional one that was
discovered in July 2013, totaling an area of 0.230 m\2\ (2.476 ft\2\)
(Possley 2013, pp. 1-2; Possley et al. 2013, pp. 43-45).
Sumter County
In Sumter County, the Rocky Hammock subpopulation contains 44
clusters, while the newly discovered subpopulation (Tree Frog Hammock)
is much smaller with only 4 clusters observed (van der Heiden and
Johnson 2014, p. 7). Average cluster size for Rocky Hammock is
estimated at 4.355 m\2\ (46.877 ft\2\) and 0.132 m\2\ (1.421 ft\2\) for
Tree Frog Hammock.
Summary of Comments and Recommendations
In the proposed rule published on October 9, 2014, we requested
that all interested parties submit written comments on the proposal by
December 8, 2014. We also contacted appropriate Federal and State
agencies, scientific experts and organizations, and other interested
parties and invited them to comment on the proposal. Newspaper notices
inviting general public comment were published in the Miami Herald. We
did not receive any requests for a public hearing. All substantive
information provided during comment periods has either been
incorporated directly into this final determination or addressed below.
Peer Reviewer Comments
In accordance with our peer review policy published on July 1, 1994
(59 FR 34270), we solicited expert opinion from five knowledgeable
individuals with scientific expertise that included familiarity with
Trichomanes punctatum ssp. floridanum and its habitat, biological
needs, and threats. We received responses from all five of the peer
reviewers.
We reviewed all comments received from the peer reviewers for
substantive issues and new information regarding the listing of
Trichomanes punctatum ssp. floridanum. The peer reviewers
[[Page 60449]]
generally concurred with our methods and conclusions and provided
additional information, clarifications, and suggestions to improve the
final rule.
(1) Comment: One peer reviewer noted that he was unaware of any
documentation that Trichomanes punctatum ssp. floridanum formed gemmae,
as stated in the proposed rule. He commented that the works cited were
in reference to other species of Trichomanes and Hymenophyllaceae, in
general. Also, the peer reviewer pointed out a reference (Hughes 2014)
in the proposal that the two metapopulations have no observable genetic
differences. The peer reviewer noted that, in the Life History section,
the proposal states many traits of the subspecies, such as ``genetic
variation,'' are unknown, which contradicts the data from Hughes.
Our Response: We appreciate this information and have corrected and
updated the rule as follows: (1) We removed the phrase that stated
Trichomanes punctatum ssp. floridanum produces gemmae; and (2) the term
genetic variation has been removed from a sentence discussing specific
reproductive and growth requirements that are unknown for the
subspecies, as it conflicted with previous information within the
proposed rule.
(2) Comment: Two peer reviewers noted that, under the Species
Description section, the proposed rule incorrectly compares physical
characteristics of Trichomanes punctatum ssp. floridanum with ``other
bryophytes.'' The phrase should only read ``bryophytes,'' not ``other
bryophytes.''
Our Response: The word ``other'' has been deleted from the text
within the Species Description section because Trichomanes punctatum
ssp. floridanum is a fern and not a bryophyte.
(3) Comment: One peer reviewer noted, under the Life History
section, that although it is true that the sporophyte form is
recognizable and spores are invisible to the naked eye, that sentence
does not align with the previous thought in the paragraph that there
are two stages, a sporophyte and a gametophyte stage.
Our Response: We have restructured the sentence and noted that the
gametophyte form is cryptic and invisible to the naked eye.
(4) Comment: One peer reviewer questioned why the two extant
populations in Sumter County (that are listed in Table 3) are not
listed in Table 2.
Our Response: Table 2 is a composite of populations that are
presumed extirpated, extirpated, or unconfirmed (where the report was
questionable). Table 3 is a summary of the known extant occurrences of
Trichomanes punctatum ssp. floridanum. The title of Table 2 has been
modified for clarity in the final rule.
(5) Comment: One peer reviewer noted that numerous efforts to
cultivate Trichomanes punctatum ssp. floridanum ex-situ for possible
future reintroduction have only been partially successful and provided
information on ex-situ reproduction efforts. The reviewer noted that,
given the problems with ex-situ reproduction, it is critical the extant
wild populations be protected to the greatest extent possible.
Our Response: We have added text explaining propagation challenges
and the importance of protecting extant populations in the wild.
Comments From the State
We received one comment from the Florida Natural Areas Inventory
regarding a discrepancy between Table 2 and Table 3. That comment is
addressed above under Peer Reviewer Comments in our response to Comment
(4).
Public Comments
We received eight public comments, three of which were from the
same individual, directly addressing the proposed listing. Most
commenters suggested technical corrections pertaining to the Background
and Summary of Factors Affecting the Species sections of the proposed
rule, scientific names, species biology, and citations. Some commenters
suggested we include additional information and correct minor errors.
We did not receive any requests for a public hearing. The comments are
appreciated, and most have been incorporated into the appropriate
sections of the final rule.
(6) Comment: Two commenters noted an inaccurate statement in the
proposed listing rule that states ``The life cycle of ferns is not well
known'' (Woodmansee, 2013, pers. comm.). One of these commenters also
noted that the second part of the same sentence mentions the life
history of Trichomanes punctatum ssp. floridanum and then includes
other members of the genus, which is inconsistent. One of these
commenters also noted that the next sentence in this paragraph is
incorrect and provided edits to describe the gametophyte form and the
sporophyte form.
Our Response: We revised the language regarding the life cycle of
the Trichomanes punctatum ssp. floridanum in the Life History section
from not well known to not commonly understood, as suggested by one of
the commenters. The second part of the sentence, which includes
information on other members of the genus Trichomanes, is unnecessary
and has been removed. We have also revised the last sentence in that
paragraph to best describe the gametophyte and sporophyte forms.
(7) Comment: One commenter noted that Trichomanes punctatum ssp.
floridanum bristles do not protrude from the sporangia, but rather one
bristle protrudes from each soral involucre, which is the tube that
also houses the sporangia.
Response: We have corrected this information in the Background
section of this final rule.
(8) Comment: Two commenters noted that the four populations of
Trichomanes punctatum ssp. floridanum within the urban preserves of
Miami-Dade County are cooperatively managed by Miami-Dade County's EEL
Program as well as the NAM Division of Miami-Dade County. One of these
commenters suggested specific edits to sections about the EEL Program
and the EEL Covenant Program. Both commenters provided additional
information and clarification about the impacts of Hurricane Andrew on
Hattie Bauer Hammock and the recovery of the hammock.
Our Response: We agree that the NAM Division of the Miami-Dade
County PROS Department and the EEL Program are significant local
partners in the conservation of Trichomanes punctatum ssp. floridanum.
As such, their efforts have been acknowledged in the final rule. We
have incorporated suggested edits about the EEL Program, the EEL
Covenant Program, and Hattie Bauer Hammock.
(9) Comment: A commenter provided information clarifying the
historical range of the subspecies. The text in the proposed rule reads
``In Miami-Dade, the range of this subspecies extended from Royal Palm
Hammock (now in Everglades National Park (ENP)) at its southern limit,
northeast to Snapper Creek Hammock, which is located in R. Hardy
Matheson Preserve.'' The reviewer noted that portions of historical
Snapper Creek are now developed and are a residential community called
Smather's Four Fillies Farm, owned by the University of Miami.
Smather's Four Fillies Farm is located in the northwestern 6.5 acres of
what was historical Snapper Creek Hammock.
Our Response: We modified the historical range of the subspecies to
[[Page 60450]]
include the additional description of the Smather's Four Fillies Farm
residential development within the Background section of the final
rule.
(10) Comment: One commenter noted the proposed listing rule states,
in the Species Description section, that the subspecies does not have
roots and then later states, in the Life History section, that the
subspecies sends out roots and shoots. The commenter requested
clarification on this issue.
Response: The first paragraph in the Species Description section
has been modified to state that Trichomanes punctatum ssp. floridanum
is mat-forming, has root-like structures, and contains trichomes. The
Life History section has been modified to reflect that T. punctatum
ssp. floridanum is rhizomatous (having a horizontal stem and scale
leaves, bearing aerial shoots from its tips, and producing root-like
structures from its undersurface).
(11) Comment: One commenter noted that the proposed listing states
the subspecies needs high temperatures and humidity for optimum growth.
The commenter remarked that this information is vague and temperatures
above 100 [deg]F may be harmful to the subspecies.
Response: We have modified our statements regarding suitable
temperatures for Trichomanes punctatum ssp. floridanum. In addition, we
have included new humidity and temperature data recorded in two Sumter
County hammocks where Trichomanes punctatum ssp. floridanum is found.
(12) Comment: One commenter reported that Ross Hammock continues to
exist and was not destroyed by a hurricane in 1935. The same commenter
reported the canopy of Hattie Bauer has also recovered after Hurricane
Andrew.
Response: We have corrected these statements in the Background
section of this final rule.
(13) Comment: One commenter noted that we cannot definitively state
that Trichomanes punctatum ssp. floridanum is extirpated outside of the
four known populations in Miami-Dade County. It is possible that
gametophytes or undiscovered sporophytes exist outside the known extant
range, particularly in the ``Monkey Jungle'' (Cox Hammock) area.
Response: We have revised this statement in the Summary of Factors
Affecting the Species section in this final rule.
Summary of Changes From the Proposed Rule
Based on the information we received from peer reviewers and public
commenters, we made the changes listed below. Additional minor
corrections and edits were made in the text of the rule. We also
incorporated new temperature, humidity, and survey information from a
recent study conducted by the IRC in Sumter County and added
information about the Clean Water Act (CWA; 33 U.S.C. 1251 et seq.)
under Factor D. The Inadequacy of Existing Regulatory Mechanisms.
Background Section
(1) We modified the information in the rule regarding the
relationship between the bristles and the sporangia of Trichomanes
punctatum ssp. floridanum and their functions.
(2) We clarified the sentence regarding the visibility of the
sporophyte and the gametophyte of Trichomanes punctatum ssp.
floridanum.
(3) We clarified information regarding the historical extent of the
subspecies to include the addition of the current-day residential
community, Smather's Four Fillies Farm, to the description of the
Snapper Creek Hammock historical area.
(4) We added the NAM Division of Miami-Dade County's PROS
Department as cooperative managers of EEL's preserves and clarified the
difference between the EEL Program and the EEL Covenant Program.
(5) We clarified that Trichomanes punctatum ssp. floridanum does
not have roots and that the subspecies is rhizomatous.
(6) We added information regarding challenges to propagation and
the importance of protecting extant populations in the wild.
Summary of Factors Affecting the Species Section
(1) We revised the information about the impacts of the hurricane
of 1935 on the habitat at Ross Hammock and the impacts of Hurricane
Andrew on Hattie Bauer Hammock and Trichomanes punctatum ssp.
floridanum. We also included additional information about the recovery
and restoration of that habitat in Hattie Bauer Hammock after Hurricane
Andrew.
(2) We added information regarding the potential existence of
Trichomanes punctatum ssp. floridanum in Miami-Dade County outside of
the four known populations, particularly in ``Monkey Jungle'' (Cox
Hammock).
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533), and its implementing
regulations at 50 CFR part 424, set forth the procedures for adding
species to the Federal Lists of Endangered and Threatened Wildlife and
Plants. Under section 4(a)(1) of the Act, we may list a species based
on one or more 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. Listing actions may be warranted
based on any of the above threat factors, singly or in combination.
Information pertaining to Trichomanes punctatum ssp. floridanum in
relation to the five factors provided in section 4(a)(1) of the Act is
discussed below. In considering what factors might constitute threats,
we must look beyond the mere exposure of the species to the factor to
determine whether the species responds to the factor in a way that
causes actual impacts to the species. If there is exposure to a factor,
but no response, or only a positive response, that factor is not a
threat. If there is exposure and a negative response, the factor may be
a threat, meaning that it may drive or contribute to the risk of
extinction of the species such that the species warrants listing as an
endangered or threatened species as those terms are defined by the Act.
This does not necessarily require empirical proof of a threat. The
combination of exposure and some corroborating evidence of how the
species is likely impacted could suffice. The mere identification of
factors that could impact a species negatively is not sufficient to
compel a finding that listing is appropriate; we require evidence that
these factors are operative threats that act on the species to the
point that the species meets the definition of an endangered or
threatened species under the Act.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
Habitat modification and destruction, caused by human population
growth and development, agricultural conversion, regional drainage, and
canal installation, have impacted the range and abundance of
Trichomanes punctatum ssp. floridanum. Secondary effects from hydrology
and canopy changes have resulted in changes in humidity, temperature,
and existing water levels; loss of natural vegetation; and habitat
fragmentation. The modification and destruction of habitat where T.p.
ssp. floridanum was once
[[Page 60451]]
found has been extreme in most areas of Miami-Dade County; while they
have been less dramatic in Sumter County, clearing of land for
agricultural conversion and historical logging has resulted in very few
areas where the habitat has not been modified. These threats are
discussed in detail below.
Human Population Growth, Development, and Agricultural Conversion
Miami-Dade County--Rockland hammocks are considered imperiled both
locally and globally, with a limited distribution and an FNAI ranking
of G2 (imperiled globally because of rarity (6 to 20 occurrences or
fewer than 3,000 individuals) or because of vulnerability to extinction
due to some natural or manmade factor)/S2 (either very rare and local
in Florida (21-100 occurrences or fewer than 10,000 individuals) or
found locally in a restricted range or vulnerable to extinction from
other factors)) (FNAI 2010, pp. 24-26, FNAI 2013). The tremendous
development and agricultural pressures in the rapidly urbanizing
rockland hammock areas in south Florida have resulted in significant
reductions of this habitat type, which is also susceptible to fire,
frost, canopy disruption, and groundwater reduction (FNAI 2010, pp. 24-
26).
Extensive land clearing for human population growth and development
in Miami-Dade County has altered, degraded, or destroyed hundreds of
acres of this once abundant rockland hammock ecosystem. Rockland
hammocks once occurred across the Miami-Rock Ridge, usually in
association with pine rocklands, or the edges of marl prairies (areas
of thin, calcitic soil that has accumulated over limestone bedrock) or
tidal swamps (Service 1999, p. 122). Destruction of rocklands,
including rockland hammocks, has occurred since the beginning of the
1900s. Historical impacts to the environment were addressed by Small
(1938, p. 50), who called attention to the demise of Trichomanes
punctatum ssp. floridanum from habitat destruction, and Phillips (1940,
p. 167) who expressed his concern for south Florida hammocks due to the
obvious and vast amount of destruction of land in the region. Early
settlers in Florida cleared hammocks for residential development,
farming, and range for livestock, while industrial logging also
occurred in the region (Snyder et al. 1990, pp. 271-272). Consistent
burning of pinelands in Miami-Dade also encroached upon adjacent
hammocks, as in the case of Castellow Hammock (Phillips 1940, p. 167).
Habitat impacts were further exacerbated by natural stochastic events,
such as the hurricane in 1935 that impacted Ross Hammock (Phillips
1940, p. 167).
Public conservation lands play a significant role in the recovery
of rockland hammock habitat where future development and habitat
alteration are less likely than on private lands. However, these lands
could be sold off in the future and become more likely to be developed
or altered in a way that negatively impacts the subspecies and its
habitat. Additionally, rockland hammock may be found on private lands;
however, the fate of this existing habitat is unknown, as it is
dependent upon actions of individual property owners (see discussion
under Factor D). Therefore, we find that habitat loss due to population
growth, development, and agricultural conversion poses a threat to this
subspecies in Miami-Dade County.
Sumter County--In Sumter County, human population growth and
development has occurred, but to a lesser degree than in Miami-Dade
County. However, Sumter County has a long history of agriculture dating
back to the early 1860s. Generally speaking, all land that was feasible
for agriculture was cleared at some point. In particular, mesic
hammocks where Trichomanes punctatum ssp. floridanum occurs have
experienced disturbances from human activities such as logging,
understory clearing, cattle grazing, and introduction of feral hogs.
These natural mesic canopies and soils have largely been destroyed due
to their desirable locations for living, camping, and recreating. The
global and State rank for mesic hammock habitat (G3/S3) signifies it is
considered to have a restricted range or be vulnerable to extinction
from other factors (FNAI 2010, p. 22).
Concerns exist regarding future population growth and development
in those communities remaining in Sumter County and on lands where
urbanization and agriculture have not yet been established. According
to the Sumter County Comprehensive Plan, a growth management paradigm
has been developed that focuses public resources on urban areas to
protect existing undeveloped land for agricultural use (Sumter County
2012, Data and Analysis section). Currently, the threat with greatest
impact to T.p. ssp. floridanum habitat in Sumter County is the
potential for agricultural and residential clearing of mesic hammocks
on small, fragmented private parcels.
Privately owned land in the area around Wahoo where Trichomanes
punctatum ssp. floridanum is found has been zoned as ``agricultural''
on the Sumter County Future Land Use Map (Sumter County 2012, p. 42).
The County exempts single-site residential development and agriculture
from environmental review and does not regulate land clearing for a
single residence. Therefore, any undocumented populations and suitable
habitat on private lands are at risk due to land-clearing activities,
agricultural conversions, and development. For example, one Sumter
County subpopulation observed in 1999 on private land was extirpated
due to pasture clearing on the property for livestock (van der Heiden
2013c, pers. comm.). A full survey for T.p. ssp. floridanum and
associated suitable habitat is needed in Sumter County to determine the
severity of potential habitat loss on this subspecies regionally,
including the potential impact from future human population growth and
development.
Due to existing agricultural and residential clearing of mesic
hammocks and potential future clearing on private lands, habitat loss
due to human population growth, development, and agricultural
conversion poses a threat to T.p. ssp. floridanum in Sumter County.
Regional Drainage and Consumptive Use
Miami-Dade County--Landscape-level drainage has been extensive in
Miami-Dade County. In the early 1900s, drainage initiatives were
undertaken to modify land for agriculture and development. Impacts
resulted in a region-wide drop in the water table (Nauman 1986, p. 182;
Lodge 2005, p. 222), disturbing rockland hammocks and their flora
(Service 1999, pp. 3-138), including Trichomanes punctatum ssp.
floridanum. Additional stress from regional drainage for canal
construction has also contributed to the decline of this metapopulation
(Nauman 1986, p. 182; see also ``Historical Range/Distribution,''
Miami-Dade County section, above). As a consequence of the pervasive
drainage throughout Miami-Dade County, solution holes, which often
contained standing water during the rainy season, now hold much less,
if any, water during much of the year, resulting in decreased ambient
humidity levels (Phillips 1940, p. 171; Nauman 1986, p. 182; Adimey
2013a, field notes). Even though regional changes in hydrology have not
caused extirpation of T.p. ssp. floridanum at most locations, they may
have already induced stress by promoting vulnerability to other
stressors, such as periodic long-term droughts, cold
[[Page 60452]]
weather exposure, and other stochastic events. Furthermore, groundwater
levels in the vicinity of T.p ssp. floridanum are not targeted as part
of the Comprehensive Everglades Restoration Plan (CERP) (a framework
and guide to restore, protect, and preserve the water resources of
central and southern Florida, including the Everglades), and,
therefore, impacts from regional drainage are not expected to be
ameliorated by CERP. Rockland hammocks in Miami-Dade County have been
modified as a result of hydrology changes, reducing the amount of water
available to these habitats. This is an ongoing threat to T.p. ssp.
floridanum, as hammocks on limestone substrates are dependent on the
underlying water table to keep humidity levels high, especially in
limestone sinkholes (Service 1999, pp. 3-127).
Currently, the human population in Miami-Dade County is expected to
grow to more than 4 million by 2060, an annual increase of roughly
30,000 people (Zwick and Carr 2006, p. 20). Although water demands will
continue to rise with population increases, the extent of future
impacts on existing habitat and the metapopulation of Trichomanes
punctatum ssp. floridanum in Miami-Dade County is unknown at this time.
Sumter County--In Sumter County, water drawdowns have historically
been minimal. Regional modeling conducted by SWFWMD indicates less than
a 0.06-m (0.2-ft) current use of water in the Upper Floridan Aquifer
(Deangelis 2014a, 2014c, pers. comm.). No surface water withdrawals are
currently occurring in Sumter County; however, they are possible in the
future. Minimum flows and levels (MFLs), which are water withdrawal
standards to limit water use set by the regional water management
districts, are already established for the Withlacoochee River portion
of the Withlacoochee River watershed in Sumter County. Although
increases in human population and development in Sumter County may
increase water use, it is believed that changes due to drought
conditions (e.g., on the order of several feet) will have a far greater
impact on the hydrology (Deangelis 2013a, pers. comm.).
Hydrology Changes
Hydrology is a key ecosystem property that affects distribution and
viability of rare plants (Gann et al. 2009, p. 6). Hydrology changes
have extensively modified and, in some cases, destroyed habitat in
south Florida. As a result of human population growth, development,
agricultural conversion, and regional drainage, the hydrology of
Trichomanes punctatum ssp. floridanum habitat has changed drastically
and has contributed to the alteration in ambient humidity and
temperature.
For a hygrophilous (living or growing in damp places) subspecies
thought to be restricted to a consistently humid microhabitat
(Kr[ouml]mer and Kessler 2006, p. 57), high humidity is a critical
factor to its survival, so any habitat modification or destruction that
changes ambient humidity levels poses a threat to this subspecies
(Nauman 1986, p. 182). As noted above, drainage efforts implemented in
south Florida have significantly reduced historical water table levels,
altering ambient humidity in the area. It is speculated that this
subspecies may be living in discrete areas where humidity may be at the
threshold for T.p. ssp. floridanum to survive. Minor drops in ambient
humidity may limit reproduction and can negatively impact overall
health of existing metapopulations, as well as inhibit the growth of
new plants, impacting long-term viability (van der Heiden, 2013c, pers.
comm.; Possley 2013e, pers. comm.). Van der Heiden and Johnson (2014,
p. 9) recently observed this in Sumter County, where small drops in
ambient temperature and humidity resulted in observed declines in the
health of some clusters of T.p. ssp. floridanum within the local
population.
Canopy Changes
Canopy also is an important habitat feature for Trichomanes
punctatum ssp. floridanum, and, in most cases, is the primary factor
controlling surrounding temperature and humidity levels that are
critical to the survival of this subspecies. The proper amount of high
shade and low light is critical for the persistence of this subspecies.
These features help to maintain humidity and prevent desiccation from
excessive light exposure (van der Heiden 2013c, pers. comm.; Possley
2013e, pers. comm.; Adimey 2013a-b, field notes). Currently, in both
metapopulations, dense canopy cover is a necessity; however, the amount
of canopy density needed to ensure survival is not yet known. Changes
to existing canopies can result from land clearing and conversion,
natural stochastic events, competition with nonnative species, and
nonnative species control (see discussion under Factor E).
Historically, as land was developed, natural features of the
landscape changed, directly eliminating Trichomanes punctatum ssp.
floridanum and also eliminating surrounding vegetation and habitat
features essential to this subspecies. Field observations in Miami-Dade
County have found clusters of T.p. ssp. floridanum desiccated when the
immediate canopy above the ferns was destroyed or substantially
reduced, allowing high amounts of light into the understory (Possley
2013g, pers. comm.); however, over the course of many months, these
clusters eventually recovered.
The loss of canopy can result in plant desiccation via increased
sun and wind exposure, increased ambient temperatures, changes in
ambient humidity, and the proliferation of exotic species (see Factor E
discussion, below). Destruction or changes in canopy of any existing
populations could result in elimination of an entire population.
Therefore, we find the loss of canopy through habitat loss and
modification to be a threat to T.p. ssp. floridanum.
Habitat Fragmentation
Habitat fragmentation limits dispersal and population size, and
promotes vulnerability among existing populations. In Miami-Dade
County, most remaining Trichomanes punctatum ssp. floridanum habitat
(i.e., Fuchs, Meissner, Castellow, Hattie Bauer hammocks) is surrounded
by housing development and agricultural land, resulting in scattered
and small natural areas. Regional drainage and hydrology changes may
also have contributed to the fragmented habitat in Miami-Dade County.
In Sumter County, the impacts of habitat fragmentation are not as
severe, as conservation lands are on large, adjacent tracts. Future
development in Sumter County could result in an increase in fragmented
habitat and pose a threat for this northern metapopulation (van der
Heiden 2013c, pers. comm.). However, data regarding the impacts and
subsequent consequences from habitat fragmentation are incomplete for
both metapopulations of Trichomanes punctatum ssp. floridanum.
Information and understanding of dispersal mechanisms for this
subspecies are also currently lacking. The best available data for
other plant species regarding the impacts of habitat fragmentation
suggest that habitat fragmentation is likely a stressor impacting this
subspecies but does not indicate that it rises to the level of a
threat.
Conservation Efforts To Reduce Habitat Destruction, Modification, or
Curtailment of Its Range
Conservation efforts to reduce habitat destruction are generally
focused on the conservation of land on which both metapopulations
occur. All known
[[Page 60453]]
extant populations occur on State- or County-owned land that is
currently protected from future development. In Miami-Dade County,
extant occurrences of Trichomanes punctatum ssp. floridanum have been
protected through acquisition within the County's EEL Program.
Fee Title Properties
In 1990, Miami-Dade County voters approved a 2-year property tax to
fund the acquisition, protection, and maintenance of natural areas by
the EEL Program. The EEL (acquisition) Program purchases and manages
natural lands for preservation. Land uses deemed incompatible with the
protection of the natural resources are prohibited by current
regulations; however, the County Commission ultimately controls what
may happen with any County property, and land use changes may occur
over time (Gil 2013b, pers. comm.). To date, the Miami-Dade County EEL
Program has acquired a total of approximately 95 ha (236 ac) of
tropical hardwood and rockland hammocks (Gil 2013b, pers. comm.). The
EEL Program also manages approximately 639 ha (1,578 ac) of tropical
hardwood and rockland hammocks known as EEL Preserves and owned by the
Miami-Dade County PROS Department, including some of the largest
remaining areas of tropical hardwood and rockland hammocks (e.g.,
Matheson Hammock Park, Castellow Hammock Park, and Deering Estate Park
and Preserves). The EEL Program may acquire lands that were once under
an EEL Covenant (see description below). However, the existence of an
EEL Covenant is not a requirement or precursor for acquisition of lands
under the EEL Program.
EEL Covenant Program
In 1979, Miami-Dade County established the EEL Covenant Program to
reduce taxes for private landowners who own natural forest communities
(NFC), such as pine rocklands and rockland hammocks. Under the EEL
Covenant Program, landowners agree not to develop their property and to
manage it for a period of 10 years, with the option to renew for
additional 10-year periods (Service 1999, pp. 3-177). The EEL Covenant
Program currently protects approximately 119 rockland hammock
properties, comprising approximately 315.65 ha (780 ac) of habitat
(Joyner 2013b, pers. comm.).
Although these temporary conservation easements provide valuable
protection for their duration, they are not considered under Factor D,
below, because they are voluntary agreements and not regulatory in
nature. Miami-Dade County currently has approximately 21 rockland
hammock properties enrolled in this program, preserving 20.64 ha (51
ac) of rockland hammock habitat (Joyner 2013b, pers. comm.). The vast
majority of these properties are small, and many are in need of habitat
management, such as removal of nonnative, invasive plants. Although the
EEL Covenant Program has the potential to provide valuable habitat for
unknown or future populations of Trichomanes punctatum ssp. floridanum,
the actual contribution of these designated conservation lands is
largely determined by whether individual landowners follow prescribed
EEL management plans and NFC regulations (see ``Local'' under Factor D
below).
The County- and State-owned land areas that are protected by the
EEL Program are critical to providing habitat for Trichomanes punctatum
ssp. floridanum, as well as other native flora in Florida. Conservation
efforts to prevent the future extirpation of T. p. ssp. floridanum and
other fern species in Miami's EEL Preserves have been under way for
many years. In Miami-Dade County, conservation lands are and have been
monitored by Fairchild and IRC, in coordination with the EEL Program
and the NAM Division of Miami-Dade County's PROS Department, to assess
habitat status and determine any changes that may pose a threat to or
alter the abundance of T. p. ssp. floridanum (Possley 2013k, pers.
comm.; van der Heiden 2013f-h, pers. comm.). Impacts to habitat (e.g.,
canopy) via nonnative species and natural stochastic events are
monitored and actively managed in areas where the taxon is known to
occur. These programs are long term and ongoing in Miami-Dade County;
however, programs are limited by the availability of annual funding.
Other Efforts
To date, only one reintroduction of filmy ferns (no specific
species was indicated) was attempted by F.C. Craighead in the early
1960s, in several hammocks within ENP within the Long Pine Key area.
These efforts were unsuccessful, but no explanation was provided as to
why they were unsuccessful (Gann 2013). Within-range reintroductions
into unoccupied habitat have historically resulted in low success rates
for plants (Maschinski et al. 2011, p. 159). Future reintroduction
efforts will likely be attempted by MSBG from Trichomanes punctatum
ssp. floridanum plants grown in-vitro from CREW.
In Sumter County, monitoring and management in Withlacoochee State
Forest is provided through the Florida Forest Service (Werner 2013e,
pers. comm.). Habitat is assessed annually for canopy changes that may
alter ambient humidity levels and for impacts from nonnative plant
species and feral pigs. Additionally, surveys on SWFWMD property are
conducted periodically to assess habitat and search for rare plant
species in the area (Deangelis 2013b, pers. comm.).
Summary of Factor A
Past human actions have destroyed, modified, and curtailed the
range and habitat available for Trichomanes punctatum ssp. floridanum.
Human population growth and development, agricultural conversion, and
regional drainage have modified, or in most cases, destroyed, habitat
where T. p. ssp. floridanum once occurred, thereby limiting the
subspecies' current range and abundance in Florida.
In Miami-Dade County, habitat modification and destruction have
severely impacted rockland hammocks that were once abundant. The
Trichomanes punctatum ssp. floridanum metapopulation in Miami-Dade
County is currently composed of four known populations, all on County-
managed conservation lands. Historically, T. p. ssp. floridanum was
found in an additional nine hammocks in Miami-Dade County. Most of
these populations have been extirpated, and the historical range of the
southern metapopulation has been reduced by nearly 80 percent. However,
the subspecies was observed in ``Monkey Jungle'' (historically referred
to as Cox Hammock) in 1989, and no thorough surveys have been conducted
there since then. Upon recent visitation to the site (Adimey 2013a,
field notes), the habitat features appeared to be similar to other
hammocks where T. p. ssp. floridanum is currently known to occur (large
solution holes, high humidity, dense canopy, standing water). Thus,
much of the habitat has been destroyed, and while those fragments
suitable for the plant remain protected in Miami-Dade County, habitat
loss and modification from future development or conversion on private
and conservation lands in Miami-Dade County poses a threat. In
addition, the areas where T. p. ssp. floridanum currently exists are
still vulnerable to activities in the surrounding areas, including
agricultural clearing and hydrologic alterations.
The Sumter County metapopulation of Trichomanes punctatum ssp.
floridanum is composed of two known
[[Page 60454]]
populations, both on State-owned land in the Jumper Creek Tract of the
WSF. In central Florida, the subspecies was historically found in as
many as seven additional locations. All of these historical populations
have since been extirpated, primarily due to land conversion and
clearing (including for cattle grazing) and the impacts of local and
regional drainage. Land clearing and hydrological alterations on
private lands adjacent to the Jumper Creek Tract continue to be threats
to T. p. ssp. floridanum populations and habitat.
The destruction and modification of habitat have resulted in
changes in canopy, humidity, hydrology, and fragmentation that have
contributed to the declines of this taxon. High humidity and dense
canopy cover are critical for Trichomanes punctatum ssp. floridanum's
survival. Therefore, any habitat modification or destruction that
changes ambient humidity levels or canopy cover poses a threat to this
subspecies. Data regarding the impacts of habitat fragmentation are
incomplete for both metapopulations of T. p. ssp. floridanum because
information on dispersal mechanisms of this subspecies is currently
lacking. Habitat fragmentation is likely a stressor impacting this
subspecies, but the best available data do not indicate that it rises
to the level of a threat.
Conservation efforts are currently providing some benefits to this
subspecies but are not sufficient to ameliorate the habitat threats.
Therefore, based on the best information available, we have determined
that the threats to Trichomanes punctatum ssp. floridanum from habitat
destruction, modification, or curtailment are occurring throughout the
entire range of the species and are expected to continue into the
future.
Factor B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
The best available data do not indicate that overutilization for
commercial, recreational, scientific, or educational purposes is
occurring and, therefore, we find that overutilization is not a threat
to Trichomanes punctatum ssp. floridanum.
Factor C. Disease or Predation
No diseases or incidences of predation have been reported for
Trichomanes punctatum ssp. floridanum. Therefore, the best available
data do not indicate that disease or predation is a threat to the
subspecies.
Factor D. The Inadequacy of Existing Regulatory Mechanisms
Under this factor, we examine whether threats to the subspecies
discussed under the other factors are continuing due to an inadequacy
of an existing regulatory mechanism. Section 4(b)(1)(A) of the Act
requires the Service to take into account ``those efforts, if any,
being made by any State or foreign nation, or any political subdivision
of a State or foreign nation, to protect such species . . . .'' In
relation to Factor D under the Act, we interpret this language to
require the Service to consider relevant Federal, State, and tribal
laws, regulations, and other such mechanisms that may minimize any of
the threats we describe in threat analyses under the other four
factors, or otherwise enhance conservation of the species. We give
strongest weight to statutes and their implementing regulations and to
management direction that stems from those laws and regulations. An
example would be State governmental actions enforced under a State
statute or constitution or Federal action under statute.
Having evaluated the impact of the threats as mitigated by any such
conservation efforts, we analyze under Factor D the extent to which
existing regulatory mechanisms are inadequate to address the specific
threats to the species. Regulatory mechanisms, if they exist, may
reduce or eliminate the impacts from one or more identified threats. In
this section, we review existing Federal, State, and local regulatory
mechanisms designed to address threats to Trichomanes punctatum ssp.
floridanum to determine whether they effectively reduce or remove
threats to the subspecies.
Federal
The only known extant populations of Trichomanes punctatum ssp.
floridanum occur on State- or County-owned properties, and development
of most of these areas is not likely to require a Federal permit or
other authorization.
Section 404 of the Clean Water Act (CWA; 33 U.S.C. 1251 et seq.)
establishes a Federal program for regulating the discharge of dredged
or fill material into waters of the United States, including wetlands.
Additionally, section 401 of the CWA forbids Federal agencies from
issuing a permit or license for activities that may result in a
discharge to waters of the United States until the State or Tribe where
the discharge would originate has granted or waived certification. The
State of Florida maintains regulatory programs providing a framework
for issuance of section 401 certifications related to applications for
section 404 permits. This legislation does not prohibit the discharge
of these materials into wetlands; rather, it provides a regulatory
framework that requires permits prior to such action being taken. The
U.S. Army Corps of Engineers (Corps) reviews individual permits for
potentially significant impacts; however, most discharges are
considered to have minimal impacts and may be covered by a general
permit that does not require individual review.
On June 29, 2015, the Environmental Protection Agency and Corps
published a final rule (80 FR 37054), effective August 28, 2015, that
revises the definition of ``waters of the United States.'' Specific
guidance on implementation of this revised definition is currently
lacking, but it appears that the revised definition is likely to
include hydric hammocks in areas where Trichomanes punctatum ssp.
floridanum occurs in Sumter County among waters of the United States.
However, as noted above, section 404 of the CWA does not necessarily
prevent degradation to such habitats from the discharge of dredge or
fill material. It simply provides a regulatory program for permitting
activities that would result in such a discharge. Further, discharges
associated with normal farming, ranching, and forestry activities, such
as plowing, cultivating, minor drainage, and harvesting for the
production of food, fiber, and forest products are exempt from the
requirement to obtain a permit.
State
FNAI considers the State status of Trichomanes punctatum ssp.
floridanum to be S1, ``critically imperiled in Florida because of
extreme rarity (five or fewer occurrences or less than 1,000
individuals) or because of extreme vulnerability to extinction due to
some natural or man-made factor'' (FNAI, 2013; Element Tracking
Summary). The IRC considers its status as ``critically imperiled''
(Gann et al. 2002, pp. 552-554).
The Florida Department of Agriculture and Consumer Services has
listed Trichomanes punctatum ssp. floridanum on the Regulated Plant
Index (Index) as endangered under Chapter 5B-40, Florida Administrative
Code (State of Florida 2013, Florida Statutes). This listing provides
little or no habitat protection beyond the State's Development of
Regional Impact process, which discloses impacts from projects, but
provides no regulatory
[[Page 60455]]
protection for State-listed plants on private lands.
Florida Statutes chapter 581.185, sections (3)(a) and (b), prohibit
any person from willfully destroying or harvesting any species listed
as endangered or threatened on the Index, or growing such a plant on
the private land of another, or on any public land, without first
obtaining the written permission of the landowner and a permit from the
Florida Department of Plant Industry. The statute further provides that
any person willfully destroying or harvesting; transporting, carrying,
or conveying on any public road or highway; or selling or offering for
sale any plant listed in the Index as endangered must have a permit
from the State at all times when engaged in any such activities.
Further, section (10) of the statute provides for consultation similar
to section 7 of the Act for listed species, by requiring the Department
of Transportation to notify the FDACS and the Endangered Plant Advisory
Council of planned highway construction at the time bids are first
advertised, to facilitate evaluation of the project for listed plant
populations, and to ``provide for the appropriate disposal of such
plants'' (i.e., transplanting). However, this statute provides no
substantive protection of habitat or protection of potentially suitable
habitat at this time. Sections (8)(a) and (b) of the statute waive
State regulation for certain classes of activities for all species on
the Index, including the clearing or removal of regulated plants for
agricultural, forestry, mining, construction (residential, commercial,
or infrastructure), and fire-control activities by a private landowner
or his or her agent.
The Florida Forest Service (FFS) is the lead managing agency for
State forests, as outlined in the Management Lease from the landowner
(Board of Trustees of the Internal Improvement Trust Fund of the State
of Florida) with guidance provided in chapters 253, 259, and 589 of the
Florida Statutes (State of Florida, 2013 Florida Statutes, Preservation
of Native Flora and Fauna). FFS is responsible for the management and
supervision of the multiple-use guidelines of Withlacoochee State
Forest. For research on State forest lands, prior approval is required.
Research deemed legitimate will be issued a State Forest Use Permit
(FDACS-11228) or letter of authorization (The Florida Forest Service
2013, State Forest Handbook).
Although the MFLs established by the South Florida Water Management
District (SFWMD) in southeast Florida (a separate entity from the
SWFWMD described earlier) are not directly applicable in the area of
Miami Rock Ridge where Trichomanes punctatum ssp. floridanum occurs,
they do indirectly limit ground water withdrawals in other areas of
south Florida, including other areas of the Miami Rock Ridge.
Unfortunately, MFL thresholds in place that establish water withdrawal
standards are set so low that protection measures are rarely triggered.
These low water level standards may be further exacerbated during times
of drought, resulting in even greater impacts to the water table and
the overall regional hydrology. Furthermore, MFL standards also do not
apply to wells on private property or for consumptive use. The lowering
of ground water and associated changes in local ambient humidity have
already occurred throughout south Florida and have likely contributed
to the decline of T. p. ssp. floridanum and possibly limited
distribution and resilience (i.e., ability to withstand stochastic
(random) events and recover from disturbances) of the subspecies
(Grossenbacher 2013, pers. comm.). Plants are likely to be further
stressed by the continued lowering of ground water if additional large
wells are created on private property for such activities as
agriculture or during extended periods of drought because these types
of circumstances are not regulated by the water withdrawal standards
established by the SFWMD. In general, this regulatory mechanism has not
been sufficient to reduce or remove the threat to T. p. ssp. floridanum
posed by changes in hydrology discussed under Factor A by ensuring that
current water levels will persist into the future.
Sumter County MFLs identified and adopted by the SWFWMD protect the
Withlacoochee River and the Tsala Apopka lake chain, which connects to
the Withlacoochee in the vicinity of Jumper Creek Tract where
Trichomanes punctatum ssp. floridanum occurs. Maintaining designated
MFLs will have a direct bearing on the design of future water supply
development projects, of which there are several already proposed in
Sumter County (Deangelis 2014c, pers. comm.). However, it is uncertain
how these future projects would impact extant occurrences of T. p. ssp.
floridanum or suitable habitat for the subspecies.
Local
In 1984, section 24-49 of the Code of Miami-Dade County established
regulation of County-designated NFCs. These regulations were placed on
specific properties throughout the County by an act of the Board of
County Commissioners in an effort to protect environmentally sensitive
forest lands. The Miami-Dade County Department of Regulatory and
Economic Resources (RER) has regulatory authority over these County-
designated NFCs and is charged with enforcing regulations that provide
partial protection of remaining upland forested areas designated as NFC
on the Miami Rock Ridge. NFC regulations are designed to prevent
clearing or destruction of native vegetation within preserved areas.
Miami-Dade County Code typically allows up to 10 percent of a rockland
hammock designated as NFC to be developed for properties greater than 5
acres and requires that the remaining 90 percent be placed under a
perpetual covenant for preservation purposes (Joyner 2013a, 2014, pers.
comm; Lima 2014, pers. comm.). However, for properties less than 5
acres, up to one-half an acre can be cleared if the request is deemed a
reasonable use of property; this allowance often can be greater than 10
percent of the property (Lima, 2014, pers. comm.). NFC landowners are
also required to obtain an NFC permit for any work, including removal
of nonnatives, within the boundaries of the NFC on their property. When
discovered, unpermitted work is pursued by RER through appropriate
enforcement action, and restoration is sought when possible. The NFC
program is responsible for ensuring that NFC permits are issued in
accordance with the limitations and requirements of the county code and
that appropriate NFC preserves are established and maintained in
conjunction with the issuance of an NFC permit when development occurs.
Although the NFC program is designed to protect rare and important
upland (non-wetlands) habitats in south Florida, it is a regulatory
strategy with limitations. For example, in certain circumstances where
landowners can demonstrate that limiting development to 10 percent does
not allow for ``reasonable use'' of the property, additional
development may be approved. Furthermore, Miami-Dade County Code
provides for up to 100 percent of the NFC to be developed in limited
circumstances for parcels less than 2.02 ha (5 ac) in size and requires
coordination with the landowners only if they plan to develop property
or perform work within the NFC designated area. As such, many of the
existing private forested NFC parcels remain fragmented, without
management obligations or preserve designation, as development has not
been proposed at a level that would
[[Page 60456]]
trigger the NFC regulatory requirements. Often, nonnative vegetation
over time begins to dominate and degrade the undeveloped and unmanaged
NFC landscape until it no longer meets the legal threshold of an NFC,
which requires the land to be dominated by native vegetation. When
development of such degraded NFCs is proposed, Miami-Dade County Code
requires delisting of the degraded areas as part of the development
process. Property previously designated as NFC is removed from the list
even before development is initiated because of the abundance of
nonnative species, making it no longer considered to be jurisdictional
or subject to the NFC protection requirements of the Miami-Dade County
Code (Grossenbacher 2013, pers. comm.).
Although Trichomanes punctatum ssp. floridanum is currently
afforded some protection from outright destruction on public
conservation land, changes in the surrounding landscape that affect the
subspecies are not regulated. For example, the private property known
as ``Monkey Jungle'' (historically referred to as Cox Hammock) is a
public attraction and is home to a considerable number of primate
species. Upon recent visitation to this site (Adimey 2013a, field
notes), the habitat features appeared to be similar to other hammocks
where T. p. ssp. floridanum currently is known to live (i.e., large
solution holes, high humidity, dense canopy, standing water). Although
much of the hammock has been altered to accommodate captive animals and
visitors, a significant portion of the hammock still remains untouched
and overgrown with extensive nonnative, invasive plant species.
``Monkey Jungle'' receives limited protection under the Miami-Dade
County Environmental Protection Ordinance as an NFC, where only
portions of NFCs can be cleared once a permit is obtained from the
County.
Additionally, Miami-Dade County has oversight of any work or
research completed within the local preserve areas; permits are
required for any outside work or research on County-owned lands in
order to further protect the habitat from potential direct or indirect
impacts (Gil 2013a, pers. comm.).
Under section 13-644(a)(1) of the Sumter County code, ``[m]ajor
developments shall identify and protect habitats of protected wildlife
and vegetation species,'' and in section 13-644(a)(1)2.b.2, ``[n]o
permit will be issued for development which results in unmitigated
destruction of specimens of endangered, threatened or rare species.''
Therefore, the County code prevents unmitigated destruction of
endangered, threatened, or rare species only when associated with
``major developments.'' Current zoning in the Wahoo area limits
development to one unit per 4 ha (10 ac); therefore, ``major
developments'' do not seem to be likely in that area. In general,
existing county ordinances do not prevent the conversion of habitat to
agricultural use or building on sites with endangered, threatened, or
rare plant species. Without complete survey information for Sumter
County, it is difficult to assess the extent to which unknown
occurrences and suitable habitat on private lands are at risk.
Agriculture and development are ongoing and promoted in this County,
and no regulatory mechanisms exist that protect T. p. ssp. floridanum
and its habitat on private lands.
Summary of Factor D
Currently, Trichomanes punctatum ssp. floridanum is only known to
occur on State and County lands; however, there are no regulatory
mechanisms in place that provide substantive protection of habitat or
protection of potentially suitable habitat at this time. In addition,
subsections of applicable statutes waive State regulation for private
landowners or their agents, allowing certain activities to clear or
remove species on the Index. Little, if any, protection is afforded to
T. p. ssp. floridanum by the established MFLs in south Florida, as they
are set very low, are rarely triggered, and are not applicable in the
portion of the Miami Rock Ridge where the subspecies currently lives.
Established MFLs in Sumter County can positively impact areas where T.
p. ssp. floridanum occurs, provided that these designated MFLs are
maintained when future water supply development projects are
undertaken. The NFC program in Miami is designed to protect rare and
important upland (non-wetland) habitats in south Florida. However, this
regulatory strategy has several limitations that can negatively affect
T. p. ssp. floridanum. Sumter County code prevents unmitigated
destruction of endangered, threatened, or rare species only when
associated with ``major developments'' and does not prevent conversion
of habitat to agricultural use or building on private property.
Although all known extant populations of Trichomanes punctatum ssp.
floridanum are afforded some level of protection because they are on
public conservation lands, existing regulatory mechanisms have not led
to a reduction or removal of threats posed to the subspecies by a wide
array of sources (see discussions under Factors A and E).
Factor E. Other Natural or Manmade Factors Affecting Its Continued
Existence
Other natural or manmade factors affect Trichomanes punctatum ssp.
floridanum to varying degrees. Specific threats include the spread of
nonnative, invasive species; potentially incompatible management
practices (e.g., inadvertent spraying of T. p. ssp. floridanum while
controlling for nonnatives); direct impacts to plants from recreation
and other human activities; small population size and isolation;
climate change; and the related risks from environmental stochasticity
(extreme weather). Each of these threats and its specific effect on T.
p. ssp. floridanum is discussed in detail below.
Nonnative Species
Nonnative species can stress, alter, or even destroy native species
and their habitats. The threat of nonnative plant species is ongoing
due to their: (1) Number and extent, (2) ability to out-compete native
species, (3) abundant seed sources, and (4) extensive disturbance
within habitats. Further challenges exist due to limitation of
resources to combat this threat, as well as the difficulty in managing
fragmented hammocks bordered by urban development, which often can
serve as seed sources for nonnative species (Bradley and Gann 1999, p.
13). Nonnative, invasive plants compete with native plants for space,
light, water, and nutrients, and they limit growth and abundance of
natural vegetation and can make habitat conditions unsuitable for
native plants.
In south Florida, at least 162 nonnative plant species are known to
invade rockland hammocks. Impacts are particularly severe on the Miami
Rock Ridge (Service 1999, pp. 3-135). Nonnative plant species have
significantly affected rockland hammock and mesic hammock habitats
where Trichomanes punctatum ssp. floridanum occurs and are considered
one of the threats with greatest impact to the subspecies (Snyder et
al. 1990, p. 273; Gann et al. 2002, pp. 552-554; FNAI 2010, pp. 22,
26). Nonnative plants outcompete and displace T. p. ssp. floridanum in
solution holes, and may form dense strata (layers) in the hammock,
where it is possible that the fern may be blanketed and smothered
(Possley 2014c, pers. comm.). It has also been suggested that the
insular nature of south Florida, as well as the hammocks themselves,
predispose this habitat to
[[Page 60457]]
invasion by nonnative plants (e.g., the proximity of seed sources,
which increases the volume of nonnatives and accelerates the time it
takes for the arrival and establishment of nonnatives) (Horvitz et al.
1998, p. 961).
In many Miami-Dade County parks, nonnative plant species comprise
50 percent of the flora in hammock fragments (Service 1999, pp. 3-135).
Horvitz (et al. 1998, p. 968) suggests the displacement of native
species by nonnative species in conservation and preserve areas is a
complex problem with serious impacts to biodiversity conservation.
Problematic nonnative invasive plants in Miami-Dade County associated
with Trichomanes punctatum ssp. floridanum include Schinus
terebinthifolia (Brazilian pepper), Bischofia javanica (bishop wood),
Syngonium podophyllum (American evergreen), Jasminum fluminense
(Brazilian jasmine), Rubus niveus (mysore raspberry), Thelypteris
opulenta (jeweled maiden fern), Nephrolepis multiflora (Asian
swordfern), Schefflera actinophylla (octopus tree), Jasminum dichotomum
(Gold Coast jasmine), Epipremnum pinnatum (centipede tongavine), and
Nephrolepis cordifolia (narrow swordfern) (Possley 2013g-h, pers.
comm.).
In Sumter County, the most problematic nonnative invasive species
occurring in Trichomanes punctatum ssp. floridanum habitat are
Tradescantia fluminensis (small leaf spiderwort) and Paederia foetida
(skunkvine) (Werner 2013d, pers. comm.). Furthermore, Citrus aurantium
(bitter orange) is found in this locale and is considered problematic
due to its tendency to attract feral hogs, another nonnative species
associated with extensive habitat destruction (see below). Agricultural
fields in proximity to the Sumter metapopulation are a nonnative seed
source, increasing potential encroachment of nonnative plants to the
area (Werner 2013b-c, pers. comm.).
In some instances, management of nonnative vegetation may also be
detrimental, in that nonnative species may actually provide the
necessary canopy to limit sunlight exposure and control humidity, so
that removing the nonnative species exposes the fern. In Castellow
Hammock, the majority of the shade near two of the large solution holes
containing Trichomanes punctatum ssp. floridanum is provided by giant
Schinus terebinthifolia trees; eliminating these trees could likely
result in detrimental effects to T. p. ssp. floridanum residing in the
underlying solution holes. In hammocks such as Castellow, desiccation
from excessive sun exposure due to the removal of S. terebinthifolia
canopy has already occurred. In this case, the subpopulation of T. p.
ssp. floridanum below the S. terebinthifolia tree turned brown;
however, T. p. ssp. floridanum could eventually revitalize if
sufficient canopy is reestablished to limit sunlight exposure (Possley
2013d, pers. comm.). Additionally, nonnative plant control may also
become a threat when T. p. ssp. floridanum is inadvertently sprayed
while authorities conduct local nonnative removal efforts (Possley
2013d, pers. comm.).
Nonnative plant species are also a concern on private lands, where
often these species are not controlled due to associated costs, lack of
interest, or lack of knowledge of detrimental impacts to the ecosystem.
Overall, active management is necessary to control for nonnative
species and to protect unique and rare habitat where T.p. ssp.
floridanum occurs (Snyder et al. 1990, p. 273). Treatment of nonnative
plant species should consider canopy and humidity needs of T.p. ssp.
floridanum.
Nonnative feral hogs living in the Withlacoochee State Forest are
also considered a threat to this plant. Surveys in Sumter County have
revealed evidence of hogs lying against or rubbing their bodies against
large rocks, removing existing vegetation in the process. Recently, van
der Heiden and Johnson (2014, p. 11) found one small rock where
Trichomanes punctatum ssp. floridanum had been scraped off when a hog
rubbed itself on the rock after wallowing in the mud. Furthermore,
rooting from hogs can destroy existing habitat by displacing smaller
rocks where T.p. ssp. floridanum is found to grow and potentially
damaging or eliminating a cluster (Werner 2013d, pers. comm.). In
Withlacoochee State Forest, damaged areas from feral hogs are also more
susceptible to invasion from nonnative plant species, such as Urena
lobata (Caesarweed) and Tradescantia fluminensis (small-leaf
spiderwort) (Werner 2013a, pers. comm.). If feral hogs continue to
forage in areas where T.p. ssp. floridanum lives, it is possible that
entire clusters inhabiting one rock/boulder could be eliminated.
In recent years, scientists in south Florida have noticed an
increase in sightings of the nonnative genus Zachrysia (Cuban tree
snails). Although snail grazing has not been observed on Trichomanes
punctatum ssp. floridanum, it has been documented on other rare ferns
living in the same habitat and could possibly become a threat in the
future, either by this snail or another introduced species (Possley
2013b, c, pers. comm.).
Climate Change
Climatic changes, including sea level rise (SLR), are occurring in
the State of Florida and are impacting associated plants, animals, and
habitats. The term ``climate,'' as defined by the Intergovernmental
Panel on Climate Change (IPCC), refers to the mean and variability of
different types of weather conditions over time, with 30 years being a
typical period for such measurements, although shorter or longer
periods also may be used (IPCC 2013, p. 1450). The term ``climate
change,'' thus, refers to a change in the mean or variability of one or
more measures of climate (e.g., temperature or precipitation) that
persists for an extended period, typically decades or longer, whether
the change is due to natural variability, human activity, or both (IPCC
2013, p. 1450). A recent compilation of climate change and its effects
is available from reports of the IPCC (IPCC 2013, entire).
Various changes in climate may have direct or indirect effects on
species. These effects may be positive, neutral, or negative, and they
may change over time, depending on the species and other relevant
considerations, such as interactions of climate with other variables
(e.g., habitat fragmentation) (IPCC 2007, pp. 8-14, 18-19). Projected
changes in climate and related impacts can vary substantially across
and within different regions of the world (e.g., IPCC 2007, p. 8-12).
Therefore, we use ``downscaled'' projections when they are available
and have been developed through appropriate scientific procedures (see
Glick et al. 2011, pp. 58-61, for a discussion of downscaling). As to
Trichomanes punctatum ssp. floridanum, downscaled projections suggest
that SLR is the largest climate-driven challenge to low-lying coastal
areas in the subtropical ecoregion of southern Florida (U.S. Climate
Change Science Program (USCCSP) 2008, pp. 5-31, 5-32). All Miami-Dade
County populations of T.p. ssp. floridanum occur at elevations 2.83-
4.14 m (9.29-13.57 ft) above sea level, making the subspecies highly
susceptible to increased storm surges and related impacts associated
with SLR, whereas the Sumter County populations are at approximately
10.40 m (34.12 ft) above sea level and significantly farther from the
coast.
The long-term record at Key West shows that sea level rose on
average 0.229 cm (0.090 in) annually between 1913 and 2013 (National
Oceanographic and Atmospheric Administration
[[Page 60458]]
(NOAA) 2013, p. 1). This equates to approximately 22.9 cm (9.02 in)
over the last 100 years. IPCC (2008, p. 28) emphasized it is very
likely that the average rate of SLR during the 21st century will exceed
the historical rate. The IPCC Special Report on Emission Scenarios
(2000, entire) presented a range of scenarios based on the computed
amount of change in the climate system due to various potential amounts
of anthropogenic greenhouse gases and aerosols in 2100. Each scenario
describes a future world with varying levels of atmospheric pollution
leading to corresponding levels of global warming and corresponding
levels of SLR. The IPCC Synthesis Report (2007, entire) provided an
integrated view of climate change and presented updated projections of
future climate change and related impacts under different scenarios.
Subsequent to the 2007 IPCC Report, the scientific community has
continued to model SLR. Recent peer-reviewed publications indicate a
movement toward increased acceleration of SLR. Observed SLR rates are
already trending along the higher end of the 2007 IPCC estimates, and
it is now widely held that SLR will exceed the levels projected by the
IPCC (Rahmstorf et al. 2012, p. 1; Grinsted et al. 2010, p. 470). Taken
together, these studies support the use of higher end estimates now
prevalent in the scientific literature. Recent studies have estimated
global mean SLR of 1.0-2.0 m (3.3-6.6 ft) by 2100 as follows: 0.75-1.90
m (2.50-6.20 ft; Vermeer and Rahmstorf 2009, p. 21530), 0.8-2.0 m (2.6-
6.6 ft; Pfeffer et al. 2008, p. 1342), 0.9-1.3 m (3.0-4.3 ft; Grinsted
et al. 2010, pp. 469-470), 0.6-1.6 m (2.0-5.2 ft; Jevrejeva et al.
2010, p. 4), and 0.5-1.4 m (1.6-4.6 ft; National Research Council 2012,
p. 2).
Other processes expected to be affected by projected warming
include temperatures, rainfall (amount, seasonal timing, and
distribution), and storms (frequency and intensity) (see
``Environmental Stochasticity,'' below). Models where sea level
temperatures are increasing also show a higher probability of more
intense storms (Maschinski et al. 2011, p. 148). The Massachusetts
Institute of Technology (MIT) modeled several scenarios combining
various levels of SLR, temperature change, and precipitation
differences with human population growth, policy assumptions, and
conservation funding changes (see ``Alternative Future Landscape
Models,'' below). All of the scenarios, from small climate change
shifts to major changes, indicate significant effects on coastal Miami-
Dade County. The Science and Technology Committee of the Miami-Dade
County Climate Change Task Force (Wanless et al. 2008, p. 1) recognizes
that significant SLR is a serious concern for Miami-Dade County in the
near future. In a January 2008 statement, the committee warned that sea
level is expected to rise at least 0.9-1.5 m (3.0-5.0 ft) within this
century (Wanless et al. 2008, p. 3). With a 0.9-1.2 m (3.0-4.0 ft) rise
in sea level (above baseline) in Miami-Dade County, spring high tides
would be at about 1.83-2.13 m (6.0-7.0 ft); freshwater resources would
be gone; the Everglades would be inundated on the west side of Miami-
Dade County; the barrier islands would be largely inundated; storm
surges would be devastating to coastal habitat and associated species;
and landfill sites would be exposed to erosion, contaminating marine
and coastal environments. Freshwater and coastal mangrove wetlands will
be unable to keep up with or offset SLR of 0.61 m (2.0 ft) per century
or greater. With a 1.52-m (5.0-ft) rise, Miami-Dade County will be
extremely diminished (Wanless et al. 2008, pp. 3-4).
Prior to inundations from SLR, there will likely be habitat
transitions related to climate change, including changes to hydrology
and increasing vulnerability to storm surge. Hydrology has a strong
influence on plant distribution in coastal areas (IPCC 2008, p. 57).
Such communities typically grade from salt to brackish to freshwater
species. From the 1930s to 1950s, increased salinity of coastal waters
contributed to the decline of cabbage palm forests in southwest Florida
(Williams et al. 1999, pp. 2056-2059), expansion of mangroves into
adjacent marshes in the Everglades (Ross et al. 2000, pp. 101, 111),
and loss of pine rockland in the Keys (Ross et al.1994, pp. 144, 151-
155). In Florida, pine rocklands transition into rockland hammocks,
and, as such, these habitat types are closely associated in the
landscape. A study conducted in one pine rockland location in the
Florida Keys (with an average elevation of 0.89 m (2.90 ft)) found an
approximately 65 percent reduction in an area occupied by South Florida
slash pine over a 70-year period, with pine mortality and subsequent
increased proportions of halophytic (salt-loving) plants occurring
earlier at the lower elevations (Ross et al. 1994, pp. 149-152). During
this same time span, local sea level had risen by 15 cm (6 in), and
Ross et al. (1994, p. 152) found evidence of ground water and soil
water salinization.
Extrapolating this situation to hardwood hammocks is not
straightforward, but it suggests that changes in rockland hammock
species composition may not be an issue in the immediate future (5-10
years); however, over the long term (within the next 10-50 years), it
may be an issue if current projections of SLR occur and freshwater
inputs are not sufficient to maintain high humidities and prevent
changes in existing canopy species through salinization (Saha et al.
2011, pp. 22-25). Ross et al. (2009, pp. 471-478) suggested that
interactions between SLR and pulse disturbances (e.g., storm surges)
can cause vegetation to change sooner than projected based on sea level
alone. Patterns of human development will also likely be significant
factors influencing whether natural communities can move and persist
(IPCC 2008, p. 57; USCCSP 2008, p. 7-6).
Impacts from climate change, including regional SLR, have been
studied for coastal hammocks, but not rockland hammock habitat. Saha
(et al. 2011, pp. 24-25) conducted a risk assessment on rare plant
species in ENP and found that impacts from SLR have significant effects
on imperiled taxa. This study also predicted a decline in the extent of
coastal hammocks with initial SLR, coupled with a reduction in
freshwater recharge volume and an increase in pore water (water filling
spaces between grains of sediment) salinity, which will push hardwood
species to the edge of their drought (freshwater shortage and
physiological) tolerance, jeopardizing critically imperiled and/or
endemic species with possible extirpation. In south Florida, SLR of 1-2
m (0.30-0.61 ft) is estimated by 2100, which is on the higher end of
global estimates for SLR. These projected increases in sea level pose a
threat to coastal plant communities and habitats from mangroves at sea
level to salinity-intolerant, coastal rockland hammocks where
elevations are generally less than 2.00 m (6.1 ft) above sea level
(Saha et al. 2011, p. 2). Loss or degradation of these habitats can be
a direct result of SLR or a combination of several other factors,
including diversion of freshwater flow, hurricanes, and exotic plant
species infestations, which can ultimately pose a threat to rare plant
populations (Saha et al. 2011, p. 24).
Saha (et al. 2011, p. 4) suggested that the rising water table
accompanying SLR will shrink the vadose zone (the area that extends
from the top of the ground surface to the water table); increase
salinity in the bottom portion of the freshwater lens (a convex layer
of fresh ground water that floats on top of denser saltwater), thereby
increasing brackishness of plant-available water; and influence tree
species composition
[[Page 60459]]
of hardwood hammocks based upon species-level tolerance to salinity
and/or drought. Evidence of population declines and shifts in rare
plant communities, along with multi-trophic effects, already have been
documented on the low-elevation islands of the Florida Keys (Maschinski
et al. 2011, p. 148). Altered freshwater inputs can lead to the
disappearance or decline of critically imperiled coastal plant species.
Shifts in freshwater flows, annual precipitation, and variability in
SLR can impact salinity regimes. Although it is unknown if salinity
changes will impact existing habitat where T. p. ssp. floridanum
currently lives, it should be noted that salinity-intolerant plants can
become stressed within a few weeks from exposure to saline conditions,
and persistent conditions can promote colonization by more salinity-
tolerant species, thereby leading to an irreversible composition
change, even if the salinity is lower over subsequent years (Saha et
al. 2011, p. 23).
In some areas of south Florida, precipitation is the main source of
fresh water. Predictive climate change models demonstrate periods of
drought will pose a threat to existing populations of Trichomanes
punctatum ssp. floridanum. Saha (et al. 2011, pp. 19-21) found that
during times of drought and resultant salinity stress, coastal hardwood
tree density from the canopy was lost, while other species showed an
increase. Areas with a deeper freshwater lens, such as rockland
hammocks, may be able to sustain vegetation during periods of drought;
however, whether this theory is true is currently unknown. Some tree
species in coastal hammocks have the ability to access pockets of fresh
water and tolerate mild salinities. These initial responses to salinity
increases may trigger responses similar to drought, while prolonged
exposure may cause irreversible toxicity caused by accumulation of
salts (Munns 2002, p. 248), causing a reduction in canopy or mortality
(Maschinski et al. 2009, entire paper). Impacts from climate change
causing shifts in local plant communities and invasion of additional
nonnative plant species may be lessened by the ability of hardwood
hammocks (such as rockland hammocks) to harvest rainfall water and
retain it in the highly organic soil and lower their transpiration
(i.e., the process of water movement through a plant and its
evaporation from leaves and stems) during the dry season (Saha et al.
2011, p. 24).
Drier conditions and increased variability in precipitation
associated with climate change are expected to hamper successful
regeneration of forests and cause shifts in vegetation types through
time (Wear and Greis 2012, p. 39). With regard to Trichomanes punctatum
ssp. floridanum, any weather shifts causing less precipitation would
likely impact the viability of existing populations and could
potentially limit future reproduction if droughts were to become a
common occurrence. Ecosystem shifts would result in rockland and mesic
hammocks having drier conditions, regular droughts, and changes in
humidity, temperature, and canopy. Increases in the scale, frequency,
or severity of droughts and wildfires (see ``Fires'' section, below)
could have negative effects on this taxon considering its general
vulnerability due to small population size, restricted range, few
populations, and relative isolation.
Climate change impacts specifically for Trichomanes punctatum ssp.
floridanum may be numerous and vary depending on factors such as
severity, the speed at which climate changes occur, timing, health of
the species, and habitat and tolerance of species. Overall, management
of healthy ecosystems can support greater biodiversity, which is
considered one of the best strategies to combat impacts of climate
change. Removing nonnative plants and minimizing natural disturbance
impacts and other external stresses can improve the subspecies'
response to climate change impacts (Maschinski et al. 2011, p. 159). In
general, the best ways to prepare and protect rare species, such as T.
p. ssp. floridanum, from impacts of climate change include actively
managing habitats to improve population growth and potential for
natural dispersal, and controlling for nonnative species. Efforts to
actively manage for T. p. ssp. floridanum are currently limited for
both metapopulations due to logistical feasibility (e.g., dense forest,
difficulty locating populations), insufficient funding and research,
small and fragmented existing populations, and lack of successful
reintroduction efforts into the wild.
Alternative Future Landscape Models
To accommodate the high uncertainty in SLR projections, researchers
must estimate effects from a range of scenarios. Various model
scenarios developed at MIT and GeoAdaptive Inc. have projected possible
trajectories of future transformation of the peninsular Florida
landscape by 2060 based upon four main drivers: Climate change, shifts
in planning approaches and regulations, human population change, and
variations in financial resources for conservation (Vargas-Moreno and
Flaxman 2010, pp. 1-6). The scenarios do not account for temperature,
precipitation, or species habitat shifts due to climate change, and no
storm surge effects are considered. The current MIT scenarios in
Florida range from an increase in sea level of 0.09-1.0 m (0.3-3.3 ft)
by 2060.
Based on the most recent estimates of SLR and the best available
data at this time, we evaluated potential effects of SLR using the
current ``worst case'' (e.g., the highest range for SLR) MIT scenario,
as well as comparing elevations of remaining rockland hammock fragments
in Miami-Dade County and mesic hammocks in Sumter County with extant
populations of Trichomanes punctatum ssp. floridanum. The ``worst
case'' MIT scenario assumes SLR of 1.0 m (3.3 ft) by 2060, low
financial resources, a `business as usual' approach to planning, and a
doubling of human population.
Based on the 1.0-m (3.3-ft) scenario, none of the rockland hammocks
in Miami-Dade County where extant populations of Trichomanes punctatum
ssp. floridanum occur would be inundated. However, all four populations
would be within 9.66 km (6.0 mi) of saltwater, increasing the
likelihood of localized vegetation shifts within the rockland hammocks
and vulnerability to natural stochastic events such as hurricanes and
tropical storms. The 1.0-m SLR scenario shows existing rockland
hammocks in Miami-Dade County (that do not contain T.p. ssp.
floridanum) directly adjacent to saltwater. Although these existing
hammocks are located in higher elevation areas along the coastal ridge,
changes in the salinity of the water table and soils, along with
additional vegetation shifts in the region, are likely. A few remaining
rockland hammocks further inland (e.g., Big and Little George Hammocks)
are located in highly urbanized areas; these hammocks are small and
fragmented, reducing the chances of further development due to SLR in
the area. Actual impacts may be greater or less than anticipated based
upon the high variability of factors involved (e.g., SLR, human
population growth) and the assumptions made in this model.
A projected SLR (using elevation data) of 2.0 m (6.6 ft) appears to
inundate much larger portions of urban Miami-Dade County. This
evaluation was not based on any modeling, as opposed to the previous
1.0-m scenario; rather, this scenario examines current elevation based
on LiDAR (remote sensing technology that measures distance by
[[Page 60460]]
illuminating a target with a laser and analyzing the reflected light)
data. Under this 2.0-m (6.6-ft) SLR scenario, none of the four hammocks
where Trichomanes punctatum ssp. floridanum is known to occur will be
inundated, but all will be within approximately 2.41 km (1.5 mi) of
saltwater in the inundated transverse glades joining the enlarged
Biscayne Bay. Castellow Hammock will be the least impacted at
approximately 2.41 km (1.5 mi) from saltwater, while Hattie Bauer will
be adjacent to saltwater. Fuchs and Meissner hammocks will be 1.61 km
(1.0 mi) from saltwater and will be surrounded by more wetlands. This
scenario will leave all these locations extremely vulnerable to
vegetation shifts, natural stochastic events, and loss of existing
habitat and land protection. Of the remaining rockland hammocks not
containing T.p. ssp. floridanum in south Florida, most would be fully
or partially inundated after a 2.0-m (6.6-ft) SLR, except for the
hammocks located on the higher elevated coastal ridge, which would
still be adjacent to saltwater.
Due to the higher elevation and inland location of Sumter County in
north Florida, existing populations of Trichomanes punctatum ssp.
floridanum and associated habitat will not be impacted by 1.0- and 2.0-
m (3.3- and 6.6-ft) rises in sea level. The 2.0-m (6.6-ft) SLR scenario
would still leave the Sumter occurrences approximately 37.0 km (23.0
mi) from saltwater. Regional shifts in water table salinity, soils, or
vegetation are not expected.
Environmental Stochasticity
Endemic species whose populations exhibit a high degree of
isolation, such as Trichomanes punctatum ssp. floridanum, are extremely
vulnerable to extinction from both random and nonrandom catastrophic
natural or human-caused events. Small populations of species, without
positive growth rates, are considered to have a high extinction risk
from site-specific demographic (variability in population growth rates
arising from random differences among individuals in survival and
reproduction within a season) and environmental (unpredictable changes
in environmental conditions such as weather, food supply, or predators)
stochasticity (Lande 1993, pp. 911-927). Populations at the edge of a
species' range, as may be the case with T.p. ssp. floridanum in Sumter
County, may be particularly vulnerable to environmental stochasticity,
as they may also be at the edge of their physiological and adaptive
limits (Baguette 2004, p. 216).
The climate in Florida is driven by a combination of local,
regional, and global events, regimes, and oscillations (e.g., El
Ni[ntilde]o Southern Oscillation with a frequency of every 4 to 7
years, solar cycle every 11 years, and the Atlantic Multi-decadal
Oscillation); however, the exact magnitude, direction, and distribution
of these climatic influences on a regional level are difficult to
project. There are three main ``seasons'' in Florida: (1) The wet
season, which is hot, rainy, and humid from June through October; (2)
the official hurricane season that extends 1 month beyond the wet
season (June 1 through November 30), with peak season being August and
September; and (3) the dry season, which is drier and cooler, from
November through May (Miller 2013, pers. comm.). In the dry season,
periodic surges of cool and dry continental air masses influence the
weather with short-duration rain events followed by long periods of dry
weather.
Florida is considered the most vulnerable State in the United
States to hurricanes and tropical storms (Florida Climate Center,
https://coaps.fsu.edu/climate_center). Based on data gathered from 1856
to 2008, Klotzbach and Gray (2009, p. 28) calculated the climatological
probabilities for each State being impacted by a hurricane or major
hurricane in all years over the 152-year timespan. Of the coastal
States analyzed, Florida had the highest climatological probabilities,
with a 51 percent probability of a hurricane (Category 1 or 2) and a 21
percent probability of a major hurricane (Category 3 or higher). From
1856 to 2008, Florida experienced 109 hurricanes and 36 major
hurricanes. Given the few isolated populations and restricted range of
Trichomanes punctatum ssp. floridanum in locations prone to storm
influences (i.e., Miami-Dade County), this subspecies is at substantial
risk from hurricanes, storm surges, and other extreme weather events.
Natural stochastic events can pose a threat to the persistence of
Trichomanes punctatum ssp. floridanum through the destruction of
existing habitat. Some climate change models predict increased
frequency and duration of severe storms, including hurricanes and
tropical storms (McLaughlin et al. 2002, p. 6074; Cook et al. 2004, p.
1015; Golladay et al. 2004, p. 504). Other models predict that
hurricane and tropical storm frequencies in the Atlantic will decrease
between 10-30 percent by 2100 (Knutson et al. 2008, pp. 1-21). For
those models that predict fewer hurricanes, hurricane wind speeds are
expected to increase by 5-10 percent due to an increase in available
energy for intense storms. Increases in hurricane winds can elevate the
chances of damage to existing canopy.
In south Florida, tropical hardwood hammock forests are known to
experience frequent disturbances from hurricanes (Horvitz et al. 1998,
p. 947). Hurricanes and tropical storms can damage existing canopy,
which provides shade and cover from wind. Canopy loss of any kind is
determined to be the threat with greatest impact to existing
metapopulations of Trichomanes punctatum ssp. floridanum (Adimey 2013b,
field notes; Possley 2013l, pers. comm.). For example, impacts from
Hurricane Andrew in 1992 may have been responsible for the temporary
loss of the subspecies from Hattie Bauer Hammock, where it had been
observed for many years. Following this hurricane, the canopy was
damaged, allowing increased exposure to sunlight for several years.
T.p. ssp. floridanum was not seen again in Hattie Bauer Hammock until
2011 (Possley 2013l, pers. comm.). Through natural recovery, assisted
by active management activities by the EEL Program and PROS-NAM, a
large portion of the Hattie Bauer Hammock canopy has been restored to
pre-hurricane Andrew conditions (Guerra 2014, pers. comm.). Destruction
of habitat due to hurricanes has also been documented in Sumter County
in the Indian Ledges Hammock located near the town of Wahoo. This
hammock, known to host a variety of rare ferns, orchids, and large
trees, sustained severe damage from several hurricanes in 2004; very
few native plant species once found in Indian Ledges Hammock exist in
this location today (Deangelis 2014a, pers. comm.).
Historically, Trichomanes punctatum ssp. floridanum may have
benefitted from more abundant and contiguous habitat to buffer it from
storm events. The destruction and modification of native habitat,
combined with the subspecies' small population sizes, has likely
contributed over time to the stress, decline, and, in some instances,
extirpation of populations or local occurrences due to stochastic
events.
A study conducted by Horvitz et al. (1998, p. 947) found that the
regeneration of forest species after stochastic events depended on the
amount of canopy disturbance, the time since disturbance, and the
biological relationship between the individual species and its
environment. Following Hurricane Andrew, the relative abundance and
life stage changed for
[[Page 60461]]
many nonnative plant species within Miami-Dade County. These shifts
continued to occur as a result of subsequent stochastic events,
suggesting hurricanes can alter long-term hammock structure and the
ongoing changes in species composition (Horvitz et al. 1998, pp. 961,
966).
Stochastic events resulting in changes in normal precipitation
(amount, seasonal timing, and distribution) and extreme temperature
fluctuations may also impact Trichomanes punctatum ssp. floridanum.
During the winter dry season, T.p. ssp. floridanum can become
desiccated without periodic rainfall and then recover during the wet
season. Multiyear droughts may negatively impact populations. While
droughts are natural events, they are a threat because there are so few
populations of this subspecies. Specific parameters regarding humidity,
temperature, and precipitation requirements are not known at this time
for T.p. ssp. floridanum, making it difficult to accurately determine
what impacts will occur from modifications in current environmental
conditions where extant metapopulations occur. Extreme temperature
changes such as cold events in south Florida or freezing temperatures
in central Florida could have devastating impacts on this subspecies.
The small size of each population makes this plant especially
vulnerable, in which the loss of even a few individuals could reduce
the viability of a single population.
Due to the small size of existing populations of Trichomanes
punctatum ssp. floridanum and its limited genetic variability, the
subspecies' overall ability to respond and adapt to threats is likely
low. These factors, combined with additional stress from habitat
modifications (e.g., hydrological changes) may increase the inherent
risk posed by stochastic events that impact this subspecies (Matthies
et al. 2004, pp. 481-488). Additionally, stochastic events are expected
to exacerbate the impacts of regional drainage and subsequent drops in
humidity. For these reasons, T.p. ssp. floridanum is at risk of
extirpation during extreme stochastic events. We have determined that
these natural stochastic events coupled with existing small population
sizes, as addressed above, are a threat to the subspecies (Adimey
2013b, field notes; Possley 2013l, pers. comm.).
Fires
Although fires are not a current concern for existing populations
of Trichomanes punctatum ssp. floridanum, they have been known to
impact populations in the past. Craighead (1963, p. 39) noted that
extensive fires in hammocks eliminated ferns in much of their former
range. Drainage efforts in the early 1900s also increased the
occurrence of fire, as lands became drier. Phillips (1940, p. 166)
noted that the frequent occurrence of fires in the late 1930s in
southern Florida resulted in widespread destruction of flora. Fires may
have been a factor in the disappearance of this taxon in Royal Palm
Hammock, which suffered multiple fires in the first half of the 1900s
according to photographs from J.K. Small (1917; Florida Memory, State
Library and Archives of Florida; Tallahassee, Florida). In recent
decades, wildfires have been controlled in most rockland hammocks due
to the extensive urbanization in Miami-Dade County. However, fires do
have the potential to impact T.p. ssp. floridanum during periods of
prolonged drought. While fires are a natural component of some
ecosystems in south Florida, fires in hammocks can set back succession
to pine rockland or other communities and will directly kill many plant
species that are not adapted to fires, such as T.p. ssp. floridanum.
Generally, hammock environments are considered less susceptible to
wildfires because their shaded, humid microclimate is not conducive to
fire spread (Snyder et al. 1990, p. 258). Additionally, rockland
hammocks occupy elevated, rarely inundated, and fire-free sites in all
three of the major rockland areas in south Florida (Snyder et al. 1990,
p. 239). Mesic hammocks are also considered fire resistant in that many
occur as ``islands'' on high ground within basin or floodplain
wetlands, as patches of oak/palm forest in dry prairie or flatwoods
communities, on river levees, or in ecotones between wetlands and
upland communities, and possess high-moisture soils due to heavy
shading of the ground layer and accumulation of litter (FNAI 2010, p.
20). Additionally, wildfires are now considered a minor stressor in
mesic hammocks because of the use of prescribed burns within the last
15 years (Werner 2013d, pers. comm.).
Snyder (et al. 1990, p. 238) points out that the high organic
content of hammock soils in south Florida can enable the soil to burn;
however, soil fires typically only burn in hammocks in times of drought
or when fires are intentionally set (Snyder et al. 1990, pp. 258-260).
This stressor is considered minimal in that fires typically will go out
when they reach hammock margins, whether entering from pineland or some
other community due to the presence of hardwood leaf litter lying
directly on moist organic soil with minimal herbaceous fuel.
Although wildfires are known to occur in Miami-Dade and Sumter
Counties, they are not currently considered a threat at this time due
to regional prescribed burn efforts that help minimize the occurrence
of wildfires, the natural fire-resistant features of these two
habitats, and, in Sumter County, hydric hammock (less likely to burn)
surrounding Trichomanes punctatum ssp. floridanum populations.
Public Use/Encroachment
In Miami-Dade County, two of the four hammocks containing
Trichomanes punctatum ssp. floridanum (Castellow and Hattie Bauer) are
accessible to the public. However, in both cases, T.p. ssp. floridanum
is not accessible from the nature trail (Possley 2013g, pers. comm.).
If public use were to increase significantly at any of the Miami-Dade
hammocks, populations of T.p. ssp. floridanum could become at risk. For
example, because the taxon grows along the rim and walls of solution
holes, people climbing into these holes could damage existing
populations; increased use could also introduce additional nonnative
seed sources into the habitat. Similarly, climbing on boulders where
the fern occurs in Sumter County could also cause damage. However, due
to the low amount of visitation at the Withlacoochee State Forest
(Werner 2013b-c, pers. comm.), public use and encroachment do not
appear to be occurring at this time, and we have determined they do not
pose a threat to T.p. ssp. floridanum.
Small Population Size Effects and Isolation
Small, isolated populations are more susceptible to impacts
overall, and relatively more vulnerable to extinction due to genetic
problems, demographic and environmental fluctuations, and natural
catastrophes (Primack 1993, p. 255). That is, the smaller a population
becomes, the more likely it is that one or more stressors could impact
a population, potentially reducing its size such that it is at
increased risk of extinction. Although robust population viability
analyses (including minimum viable population calculations) have not
been conducted for this subspecies, indications are that most existing
populations are minimal in terms of abundance and size. Lack of
dispersal between occurrences also contributes to the low resilience
for this subspecies (see ``Habitat Fragmentation'' under Factor A).
[[Page 60462]]
Limited genetic variability will also impact Trichomanes punctatum
ssp. floridanum populations. The ability of a species to adapt to
environmental change is dependent upon genetic variation, a property of
populations that derives from its members possessing different forms
(i.e., alleles) of the same gene (Primack 1998, p. 283). High genetic
diversity can enhance a species' persistence in a changing environment
(Lynch and Lande 1993, pp. 246-247). Although Trichomanes punctatum
ssp. floridanum can grow in clusters, separate clusters are not
necessarily different individuals, as they may have been connected by
one or more stems in the past (Possley 2014b, pers. comm.). Thus, a
population of T.p. ssp. floridanum containing many clusters may not
have greater genetic diversity than a population with few clusters.
Because there are only six extant populations of T.p. ssp. floridanum,
each with few plants, the genetic variability is considered low, and
the subspecies is inherently at greater risk from stochastic events and
changes in environmental conditions (Matthies et al. 2004, pp. 481-
488).
In summary, Trichomanes punctatum ssp. floridanum is impacted by
factors such as small population size, vulnerability to random
demographic fluctuations or natural catastrophes, and low genetic
diversity, which is further magnified by synergistic (interaction of
two or more components) effects with other threats, such as those
discussed above. In evaluating the stressor of small population size
effects on Trichomanes punctatum ssp. floridanum, we reviewed the
limited data available concerning abundance at each of the occurrences
across the subspecies' range. This represents a conservative
classification of small population size, as available data do not
discriminate among individual plants and life-history stages. These
small populations are at risk of adverse effects from reduced genetic
variation, an increased risk of inbreeding depression, and reduced
reproductive output. Many of these populations are small and isolated
from each other, decreasing the likelihood that they could be naturally
reestablished in the event that extirpation from one location occurs.
Conservation Efforts To Reduce Other Natural or Manmade Factors
Affecting Its Continued Existence
Miami-Dade County and the State of Florida have ongoing nonnative
plant management programs to reduce threats on public lands, as funding
and resources allow. In Miami-Dade County, nonnative, invasive plant
management is very active, with a goal to treat all publically owned
properties at least once a year and more often in many cases. Annual
monitoring of Trichomanes punctatum ssp. floridanum is conducted by
Fairchild, which records health and size of individual clusters of the
subspecies along with potential new stressors, including nonnative,
invasive species or habitat destruction; reports are forwarded to the
County preserve managers for further attention (Possley 2013l, pers.
comm.). IRC also conducts research and monitoring in multiple hammocks
within Miami-Dade County for various rare and endangered plant species.
Nonnative, invasive species are documented, along with any occurrence
of human disturbance (van der Heiden 2013i, pers. comm.). In Sumter
County, the Florida Park Service surveys each State-owned property at
least once a year to manage for nonnative plants (Werner 2013a-b, pers.
comm.). Furthermore, Withlacoochee State Forest conducts prescribed
burning on an annual basis, controlling regional wildfires in dry
swamps and mesic hammocks.
Continuing efforts to propagate Trichomanes punctatum ssp.
floridanum in-vitro may eventually lead to the establishment of healthy
populations that can be reintroduced in locations where the taxon once
occurred or introduced to new areas deemed appropriate. These efforts
can assist with combating potential or realized impacts from natural
stochastic events that may harm or destroy existing populations.
Summary of Factor E
Stochastic events resulting in changes in canopy structure and
environmental conditions within the taxon's current habitat are
considered threats to existing and future populations of T.p. ssp.
floridanum. Droughts, tropical storms, and hurricanes are common
occurrences in Florida, and changes associated with these events have
the potential to limit reproduction and compromise overall health in
the long term, making plants more vulnerable to other stressors (e.g.,
periodic, long-term droughts, hurricanes) or causing extirpations. As
few populations remain, the entire taxon is at risk of extinction
during these events. Climatic changes, including SLR, are longer term
concerns expected to exacerbate existing impacts and ultimately reduce
the extent of available habitat for T.p. ssp. floridanum.
The presence of nonnative species, including other plants and feral
hogs, is also a threat, but may be reduced on public lands due to
active programs by Miami-Dade County and the State. The majority of the
remaining populations of this plant are small and geographically
isolated, and genetic variability is likely low, increasing the
inherent risk due to overall low resilience of this subspecies.
Furthermore, the isolated existence of Trichomanes punctatum ssp.
floridanum makes natural recolonization of extirpated populations
virtually impossible without human intervention. Although considered
stressors, wildfires and public use at extant sites are minimal and do
not rise to the level of a threat.
Cumulative Effects of Threats
When two or more threats affect Trichomanes punctatum ssp.
floridanum occurrences, the effects of those threats could interact or
become compounded, producing a cumulative adverse effect that is
greater than the impact of either threat alone. The most obvious cases
in which cumulative adverse effects would be significant are those in
which small populations (Factor E) are affected by threats that result
in destruction or modification of habitat (Factor A). The limited
distributions and small population sizes of T.p. ssp. floridanum make
it extremely susceptible to the detrimental effects of further habitat
modification, degradation, and loss, as well as other anthropogenic
threats. Mechanisms leading to the decline of this taxon, as discussed
above, range from local (e.g., hydrology changes, agriculture) to
regional (e.g., development, fragmentation, nonnative species) to
global influences (e.g., climate change, SLR). The synergistic effects
of threats, such as impacts from hurricanes on a species with a limited
distribution and small populations, make it difficult to predict
population viability. While these stressors may act in isolation, it is
more probable that many stressors are acting simultaneously (or in
combination) on populations of T.p. ssp. floridanum, making this
subspecies more vulnerable.
Determination
We have carefully assessed the best scientific and commercial data
available regarding the past, present, and future threats to
Trichomanes punctatum ssp. floridanum. T.p. ssp. floridanum has been
extirpated from the majority of its historical range, and the primary
threats of habitat destruction and modification resulting from human
population growth and development, agricultural conversion, regional
drainage, and resulting changes in canopy and hydrology (Factor A);
competition from
[[Page 60463]]
nonnative, invasive species (Factor E); changes in climatic conditions,
including sea level rise (Factor E); and natural stochastic events
(Factor E) remain threats for existing populations. Existing regulatory
mechanisms have not led to a reduction or removal of threats posed to
the subspecies from these factors (see Factor D discussion). These
threats are ongoing, rangewide, and expected to continue in the future.
Populations of T.p. ssp. floridanum are relatively small and isolated
from one another, and their ability to recolonize suitable habitat is
unlikely without human intervention. Because of the current condition
of the extant populations and life-history traits of the subspecies, it
is vulnerable to natural or human-caused changes in its currently
occupied habitats. The threats have had and will continue to have
substantial adverse effects on T.p. ssp. floridanum and its habitat.
Although attempts are ongoing to alleviate or minimize some of these
threats at certain locations, all populations appear to be impacted by
one or more threats.
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 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.'' As described in detail
above, this plant is currently at risk throughout all of its range due
to the immediacy, severity, significance, timing, and scope of those
threats. Impacts from these threats are ongoing and increasing; singly
or in combination, these threats place the subspecies in danger of
extinction. The risk of extinction is high because the populations are
small, isolated, and have limited to no capacity for recolonization.
Numerous threats are currently ongoing and are likely to continue in
the foreseeable future, at a high intensity and across the entire range
of this subspecies. Furthermore, natural stochastic events and changes
in climatic conditions pose a threat to the persistence of the
subspecies, especially because mitigation measures have yet to be
developed. Individually and collectively, all of these threats can
contribute to the local extirpation and potential extinction of this
subspecies. Because these threats are placing this subspecies in danger
of extinction throughout its range, we have determined this plant meets
the definition of an endangered species. Therefore, on the basis of the
best available scientific and commercial information, we are listing
Trichomanes punctatum ssp. floridanum as an endangered species in
accordance with sections 3(6) and 4(a)(1) of the Act. We find that a
threatened species status is not appropriate for T.p. ssp. floridanum
because of the contracted range of the subspecies and because the
threats are occurring rangewide, are currently acting on the subspecies
at a high intensity, and are expected to continue into the future.
Significant Portion of the 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. Because we have determined that
Trichomanes punctatum ssp. floridanum is an endangered species
throughout all of its range, no portion of its range can be
``significant'' for purposes of the definitions of ``endangered
species'' and ``threatened species.'' See the Final Policy on
Interpretation of the Phrase ``Significant Portion of Its Range'' in
the Endangered Species Act's Definitions of ``Endangered Species'' and
``Threatened Species'' (79 FR 37578, July 1, 2014).
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened species under the Act include recognition, recovery actions,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing results in public awareness and
conservation by Federal, State, Tribal, and local agencies, private
organizations, and individuals. The Act encourages cooperation with the
States and requires that recovery actions be carried out for all listed
species. The protection required by Federal agencies and the
prohibitions against certain activities are discussed, in part, below.
The primary purpose of the Act is the conservation of endangered
and threatened species and the ecosystems upon which they depend. The
ultimate goal of such conservation efforts is the recovery of these
listed species, so that they no longer need the protective measures of
the Act. Subsection 4(f) of the Act requires the Service to develop and
implement recovery plans for the conservation of endangered and
threatened species. The recovery planning process involves the
identification of actions that are necessary to halt or reverse the
species' decline by addressing the threats to its survival and
recovery. The goal of this process is to restore listed species to a
point where they are secure, self-sustaining, and functioning
components of their ecosystems.
Recovery planning includes the development of a recovery outline
shortly after a species is listed and preparation of a draft and final
recovery plan. The recovery outline guides the immediate implementation
of urgent recovery actions and describes the process to develop a
recovery plan. The plan may be revised to address continuing or new
threats to the species, as new substantive information becomes
available. The recovery plan identifies recovery criteria for review of
when a species may be ready for downlisting (from endangered species to
threatened species) or delisting 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 (composed of species
experts, Federal and State agencies, nongovernmental organizations, and
stakeholders) are often established to develop recovery plans. When
completed, the draft and final recovery plans will be available on our
Web site (https://www.fws.gov/endangered) or from our South Florida
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, Tribes, nongovernmental organizations, businesses,
and private landowners. Examples of recovery actions include habitat
restoration (e.g., restoration of native vegetation), research, captive
propagation and reintroduction, and outreach and education. The
recovery of many listed species cannot be accomplished solely on
Federal lands because their range may occur primarily or solely on non-
Federal lands. To achieve recovery of these species requires
cooperative conservation efforts on private, State, and Tribal lands.
Following publication of this final listing rule, funding for
recovery actions will be available from a variety of sources, including
Federal budgets, State programs, and cost share grants for non-Federal
landowners, the academic community, and nongovernmental organizations.
In addition, pursuant to section 6 of the Act, the State of Florida
will be eligible for Federal funds to implement management actions that
promote the protection or recovery of Trichomanes punctatum ssp.
floridanum. Information on our grant programs that are available to aid
species recovery can be found at: https://www.fws.gov/grants.
[[Page 60464]]
Please let us know if you are interested in participating in
recovery efforts for Trichomanes punctatum ssp. floridanum.
Additionally, we invite you to submit any new information on this
subspecies whenever it becomes available and any information you may
have for recovery planning purposes (see FOR FURTHER INFORMATION
CONTACT).
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is listed as an endangered or
threatened species 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)(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 any endangered or threatened species or destroy
or adversely modify its critical habitat. If a Federal action may
affect a listed species or its critical habitat, the responsible
Federal agency must enter into consultation with the Service.
Federal agency actions within the species' habitat that may require
conference or consultation, or both, as described in the preceding
paragraph, include, but are not limited to, federally funded or
authorized actions such as habitat restoration and control of
nonnatives management and any other landscape-altering activities on
Federal lands administered by the U.S. Fish and Wildlife Service;
issuance of section 404 Clean Water Act permits by the Army Corps of
Engineers; and construction and maintenance of roads or highways by the
Federal Highway Administration.
With respect to endangered plants, 50 CFR 17.61 makes 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 to remove and reduce to possession any such
plant species from areas under Federal jurisdiction. In addition, for
endangered plants, the Act prohibits malicious damage or destruction of
any such species on any area under Federal jurisdiction, and the
removal, cutting, digging up, or damaging or destroying of any such
species on any other area in knowing violation of any State law or
regulation, or in the course of any violation of a State criminal
trespass law. Exceptions to these prohibitions are contained in 50 CFR
17.62.
We may issue permits to carry out otherwise prohibited activities
involving endangered plants under certain circumstances. Regulations
governing permits are codified at 50 CFR 17.62. With regard to
endangered plants, the Service may issue a permit authorizing any
activity otherwise prohibited by 50 CFR 17.61 for scientific purposes
or for enhancing the propagation or survival of endangered plants.
It is our policy, as published in the Federal Register on July 1,
1994 (59 FR 34272), to identify to the maximum extent practicable at
the time a species is listed, those activities that would or would not
constitute a violation of section 9 of the Act. The intent of this
policy is to increase public awareness of the effect of a listing on
proposed and ongoing activities within the range of a listed species.
The following activities could potentially result in a violation of
section 9 of the Act. This list is not comprehensive:
(1) Import the subspecies into, or export the subspecies from, the
United States without authorization;
(2) Remove and reduce to possession the subspecies from areas under
Federal jurisdiction; maliciously damage or destroy the subspecies on
any such area; or remove, cut, dig up, or damage or destroy the
subspecies on any other area in knowing violation of any law or
regulation of any State or in the course of any violation of a State
criminal trespass law;
(3) Sell or offer for sale in interstate or foreign commerce the
subspecies; except for properly documented antique specimens of the
taxon at least 100 years old, as defined by section 10(h)(1) of the
Act;
(4) Unauthorized delivering, carrying, or transporting of the
subspecies, including import or export across State lines and
international boundaries;
(5) Introduction of nonnative species that compete with or prey
upon Trichomanes punctatum ssp. floridanum;
(6) Unauthorized release of biological control agents that attack
any life stage of this subspecies; and
(7) Unauthorized manipulation or modification of the habitat where
Trichomanes punctatum ssp. floridanum is present on Federal lands
including, but not limited to, unauthorized water withdrawal from
solution holes and unauthorized removal of canopy.
Questions regarding whether specific activities would constitute a
violation of section 9 of the Act should be directed to the South
Florida Ecological Services Field Office (see FOR FURTHER INFORMATION
CONTACT).
Critical Habitat
Section 3(5)(A) of the Act defines critical habitat as ``(i) the
specific areas within the geographical area occupied by the species, at
the time it is listed . . . 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 by the Secretary that such areas are essential for the
conservation of the species.'' Section 3(3) of the Act (16 U.S.C.
1532(3)) also defines the terms ``conserve,'' ``conserving,'' and
``conservation'' to mean ``to use and the use of all methods and
procedures which are necessary to bring any endangered species or
threatened species to the point at which the measures provided pursuant
to this chapter are no longer necessary.''
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 shall designate critical
habitat at the time the species is determined to be an endangered or
threatened species. 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.
In our proposed listing rule, because we determined that the
designation of critical habitat will not likely increase the degree of
threat to the species and may provide some measure of benefit, we
determined that designation of critical habitat is prudent for
Trichomanes punctatum ssp. floridanum.
Critical Habitat Determinability
Having determined that designation is prudent under section 4(a)(3)
of the Act, we must find whether critical habitat for Trichomanes
punctatum ssp. floridanum is determinable. Our regulations (50 CFR
424.12(a)(2)) further state that critical habitat is not determinable
when one or both of the following situations exists: (1) Information
sufficient to perform required analysis of the impacts of the
[[Page 60465]]
designation is lacking; or (2) the biological needs of the species are
not sufficiently well known to permit identification of an area as
critical habitat.
In our proposed listing rule, we found that critical habitat was
not determinable because a careful assessment of the economic impacts
that may occur due to a critical habitat designation was still ongoing,
and we were still in the process of acquiring the information needed to
perform that assessment. We have recently received new data on suitable
habitat for T. p. ssp. floridanum in Sumter County, which has caused us
to begin reassessing which specific features and areas are essential
for the conservation of the species and, therefore, meet the definition
of critical habitat. Consequently, a careful assessment of the new
biological information is still ongoing, and we are still in the
process of acquiring the information needed to perform that assessment.
The information sufficient to perform a required analysis of the
impacts of the designation is lacking, and therefore, we find
designation of critical habitat to be not determinable at this time.
Accordingly, we will publish a proposed critical habitat rule when we
finish our assessment of the new biological information.
Required Determinations
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 (42 U.S.C. 4321 et seq.), need not be prepared
in connection with listing a species as an endangered or threatened
species under the Endangered Species Act. We published a notice
outlining our reasons for this determination in the Federal Register on
October 25, 1983 (48 FR 49244).
Government-to-Government Relationship With Tribes
In accordance with the President's memorandum of April 29, 1994
(Government-to-Government Relations with Native American Tribal
Governments; 59 FR 22951), Executive Order 13175 (Consultation and
Coordination with Indian Tribal Governments), and the Department of the
Interior's manual at 512 DM 2, we readily acknowledge our
responsibility to communicate meaningfully with recognized Federal
Tribes on a government-to-government basis. In accordance with
Secretarial Order 3206 of June 5, 1997 (American Indian Tribal Rights,
Federal-Tribal Trust Responsibilities, and the Endangered Species Act),
we readily acknowledge our responsibilities to work directly with
tribes in developing programs for healthy ecosystems, to acknowledge
that tribal lands are not subject to the same controls as Federal
public lands, to remain sensitive to Indian culture, and to make
information available to tribes. We are not aware of any Trichomanes
punctatum ssp. floridanum populations on tribal lands.
References Cited
A complete list of references cited in this rulemaking is available
on the Internet at https://www.regulations.gov and upon request from the
South Florida Ecological Services Field Office (see FOR FURTHER
INFORMATION CONTACT).
Authors
The primary authors of this final rule are the staff members of the
South Florida Ecological Services Field Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Transportation.
Regulation Promulgation
Accordingly, we amend part 17, subchapter B of chapter I, title 50
of the Code of Federal Regulations, as follows:
PART 17--[AMENDED]
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; 4201-4245; unless
otherwise noted.
0
2. Amend Sec. 17.12(h) by adding an entry for ``Trichomanes punctatum
ssp. floridanum'' to the List of Endangered and Threatened Plants in
alphabetical order under Ferns and Allies to read as follows:
Sec. 17.12 Endangered and threatened plants.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species
------------------------------------------------------------ Historic range Family Status When Critical Special
Scientific name Common name listed habitat rules
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * * * *
Ferns and Allies
* * * * * * *
Trichomanes punctatum ssp. Florida bristle fern.. U.S.A. (FL)........... Hymenophyllaceae..... E 859 NA NA
floridanum.
* * * * * * *
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* * * * *
Dated: September 28, 2015.
Stephen Guertin,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2015-25299 Filed 10-5-15; 8:45 am]
BILLING CODE 4333-15-P