Endangered and Threatened Wildlife and Plants; Endangered Species Status for Trichomanes punctatum ssp. floridanum (Florida Bristle Fern), 61135-61161 [2014-23686]
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Vol. 79
Thursday,
No. 196
October 9, 2014
Part II
Department of the Interior
tkelley on DSK3SPTVN1PROD with PROPOSALS2
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);
Proposed Rules
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Federal Register / Vol. 79, No. 196 / Thursday, October 9, 2014 / Proposed Rules
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: Proposed rule.
AGENCY:
tkelley on DSK3SPTVN1PROD with PROPOSALS2
Executive Summary
We, the U.S. Fish and
Wildlife Service, propose to list
Trichomanes punctatum ssp.
floridanum (Florida bristle fern), a plant
subspecies from Miami-Dade and
Sumter Counties in Florida, as an
endangered species under the
Endangered Species Act of 1973, as
amended (Act). If we finalize this rule
as proposed, it would extend the Act’s
protections to this plant and add this
plant to the Federal List of Endangered
and Threatened Plants.
DATES: We will accept comments
received or postmarked on or before
December 8, 2014. Comments submitted
electronically using the Federal
eRulemaking Portal (see ADDRESSES
below) must be received by 11:59 p.m.
Eastern Time on the closing date. We
must receive requests for public
hearings, in writing, at the address
shown in FOR FURTHER INFORMATION
CONTACT by November 24, 2014.
ADDRESSES: You may submit comments
by one of the following methods:
(1) Electronically: Go to the Federal
eRulemaking Portal: https://
www.regulations.gov. In the Search box,
enter FWS–R4–ES–2014–0044, which is
the docket number for this rulemaking.
Then, in the Search panel on the left
side of the screen, under the Document
Type heading, click on the Proposed
Rules link to locate this document. You
may submit a comment by clicking on
‘‘Comment Now!’’
(2) By hard copy: Submit by U.S. mail
to: Public Comments Processing, Attn:
FWS–R4–ES–2014–0044; Division of
Policy and Directives Management; U.S.
Fish and Wildlife Service, MS: BPHC,
5275 Leesburg Pike, Falls Church, VA
22041–3803.
We request that you send comments
only by the methods described above.
We will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see
SUMMARY:
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Information Requested, below, for more
information).
FOR FURTHER INFORMATION CONTACT:
Craig Aubrey, 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:
Why we need to publish a rule. Under
the Endangered Species Act (Act), if we
find that a species warrants listing as an
endangered or threatened species
throughout all or a significant portion of
its range, we are required to promptly
publish a proposal in the Federal
Register and make a determination on
our proposal within 1 year. Listing a
species as an endangered or threatened
species can only be completed by
issuing a rule. In the near future, we
intend to propose to designate critical
habitat for Trichomanes punctatum ssp.
floridanum under the Act. Critical
habitat is prudent, but not determinable
at this time. We will publish a proposal
to designate critical habitat for
Trichomanes punctatum ssp.
floridanum under the Act in the near
future.
This rule proposes to list
Trichomanes punctatum ssp.
floridanum (Florida bristle fern) as an
endangered species.
The basis for our action. Under the
Act, we may 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
resulting in changes in canopy,
humidity, hydrology, and fragmentation
(Factor A); and 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).
We will seek peer review. We will seek
comments from independent specialists
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to ensure that our determination is
based on scientifically sound data,
assumptions, and analyses. We will
invite these peer reviewers to comment
on our listing proposal. Because we will
consider all comments and information
we receive during the comment period,
our final determination may differ from
this proposal.
Information Requested
Public Comments
We intend that any final action
resulting from this proposed rule will be
based on the best scientific and
commercial data available and be as
accurate and as effective as possible.
Therefore, we request comments or
information from other concerned
governmental agencies, Native
American tribes, the scientific
community, industry, or any other
interested parties concerning this
proposed rule. We particularly seek
comments concerning:
(1) Trichomanes punctatum ssp.
floridanum’s biology, range, and
population trends, including:
(a) Biological or ecological
requirements of the plant, including
habitat requirements;
(b) Genetics and taxonomy;
(c) Historical and current range,
including distribution patterns;
(d) Historical and current population
levels, and current and projected trends;
and
(e) Past and ongoing conservation
measures for the plant, its habitat, or
both.
(2) Factors that may affect the
continued existence of the plant, which
may include habitat modification or
destruction, overutilization, disease,
predation, the inadequacy of existing
regulatory mechanisms, or other natural
or manmade factors.
(3) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to this plant and
existing regulations that may be
addressing those threats.
(4) Additional information concerning
the historical and current status, range,
distribution, and population size of this
plant, including the locations of any
additional populations of the plant.
Please include sufficient information
with your submission (such as scientific
journal articles or other publications) to
allow us to verify any scientific or
commercial information you include.
Please note that submissions merely
stating support for or opposition to the
action under consideration without
providing supporting information,
although noted, will not be considered
in making a determination, as section
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4(b)(1)(A) of the Act (16 U.S.C. 1531 et
seq.) directs that determinations as to
whether any species is an endangered or
threatened species must be made
‘‘solely on the basis of the best scientific
and commercial data available.’’
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in the
ADDRESSES section. We request that you
send comments only by the methods
described in the ADDRESSES section.
If you submit information via https://
www.regulations.gov, your entire
submission—including any personal
identifying information—will be posted
on the Web site. If your submission is
made via a hardcopy that includes
personal identifying information, you
may request at the top of your document
that we withhold this information from
public review. However, we cannot
guarantee that we will be able to do so.
We will post all hardcopy submissions
on https://www.regulations.gov.
Comments and materials we receive,
as well as supporting documentation we
used in preparing this proposed rule,
will be available for public inspection
on https://www.regulations.gov, or by
appointment, during normal business
hours, at the U.S. Fish and Wildlife
Service, South Florida Ecological
Services Office (see FOR FURTHER
INFORMATION CONTACT).
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Public Hearing
Section 4(b)(5) of the Act provides for
one or more public hearings on this
proposal, if requested. Requests must be
received within 45 days after the date of
publication of this proposed rule in the
Federal Register. Such requests must be
sent to the address shown in the FOR
FURTHER INFORMATION CONTACT section.
We will schedule public hearings on
this proposal, if any are requested, and
announce the dates, times, and places of
those hearings, as well as how to obtain
reasonable accommodations, in the
Federal Register and local newspapers
at least 15 days before the hearing.
Peer Review
In accordance with our joint policy on
peer review published in the Federal
Register on July 1, 1994 (59 FR 34270),
during the public comment period we
will seek the expert opinions of
appropriate and independent specialists
regarding this proposed rule. The
purpose of peer review is to ensure that
our proposed listing determination is
based on scientifically sound data,
assumptions, and analyses. The peer
reviewers will have expertise in
Trichomanes punctatum ssp.
floridanum’s biology, habitat, and
physical or biological factors.
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Previous Federal Actions
Background
Trichomanes punctatum ssp.
floridanum was first recognized as a
candidate for possible future listing on
November 9, 2009 (74 FR 57804), and
we assigned the subspecies a listing
priority number (LPN) of 3. Candidate
species are assigned LPNs based on
immediacy and magnitude of threats, as
well as taxonomic status. The lower the
LPN, the higher priority that species is
for us to determine appropriate action
using our available resources
(September 21, 1983; 48 FR 43098). An
LPN of 3 is the lowest LPN appropriate
for a subspecies such as this fern,
indicating that it is a high priority for
the U.S. Fish and Wildlife Service
(Service) to determine appropriate
action. T. p. ssp. floridanum has
remained on the candidate list with an
LPN of 3 since 2009 (see 78 FR 70104,
November 22, 2013; 77 FR 69994,
November 21, 2012; 76 FR 66370,
October 26, 2011; 75 FR 69222,
November 10, 2010; 74 FR 57804,
November 9, 2009).
On May 10, 2011, the Service
announced a workplan to restore
biological priorities and certainty to the
listing process. As part of an agreement
with the Center for Biological Diversity
and WildEarth Guardians, we filed the
workplan with the U.S. District Court
for the District of Columbia. The
workplan will enable the agency, over a
period of 6 years, to systematically
review and address the needs of more
than 250 species, including
Trichomanes punctatum ssp.
floridanum, that were identified in our
November 10, 2010, candidate notice of
review (CNOR), published in the
Federal Register at 75 FR 69222, ssp.
floridanum to determine if these species
should be added to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. This workplan will enable
the Service to again prioritize its
workload based on the needs of
candidate species, while also providing
State wildlife agencies, stakeholders,
and other partners clarity and certainty
about when listing determinations will
be made. On July 12, 2011, the Service
reached an agreement with another
plaintiff group and further strengthened
the workplan, which will allow the
agency to focus its resources on the
species most in need of protection
under the Act. These agreements were
approved by the court on September 9,
2011. We are making this proposed
listing determination for Trichomanes
punctatum ssp. floridanum now as part
of the court-approved workplan.
It is our intent to discuss below only
those topics directly relevant to the
listing of Trichomanes punctatum ssp.
floridanum as an endangered species in
this proposed rule.
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Species Description
Trichomanes punctatum ssp.
floridanum, commonly referred to as the
Florida bristle fern, is mat-forming, has
no roots, and contains trichomes
(hairlike/bristlelike outgrowths) on the
tip of the fern (Wunderlin and Hansen
2000, pp. 153–154). This subspecies is
very small in size and superficially
resembles other bryophytes, such as
mosses and liverworts, making it
difficult to observe in its natural habitat.
T. p. ssp. floridanum has thin veinlets
(small veins) that are not enlarged
towards the margin while veins are
uniform in width to their apices (tips)
(Nauman 1986, p. 179); fronds (leaves of
ferns) are considered simple (Morton
1963, p. 89).
Wunderlin and Hansen (2000, pp.
153–154) described Trichomanes
punctatum ssp. floridanum as having
separated 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.
This subspecies has few false veins, and
its true veins are not enlarged at their
apex.
One unique characteristic of this plant
is that it lacks cuticles (the protective
layer that cover the epidermis, which is
the outermost layer of cells that cover
the leaves) or has highly reduced
cuticles, and has differentiated
epidermises and stomata (small
openings in leaves and stems through
which gases are exchanged), causing
dependence 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 spp. to shaded areas with
high humid forested environments,
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
generally lack ecological information
(Nauman 1986, p. 179; Nelson 2000, p.
77). The genus belongs to the family
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Hymenophyllaceae and the
hymenophylloid clade, where ferns are
also referred to as filmy ferns, which
represents the thin, filmy leaves of the
species (Nelson 2000, p. 77). The
common name, bristle fern, is used to
reference the bristlelike structure that
protrudes from the mature sporangia (a
structure that holds and produces
spores) (Nelson 2000, p. 77).
Five species commonly known as
bristle ferns (Trichomanes spp.) 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 plants in Florida
represented the same taxon, not two
separate species, and that T. sphenoides
(which he described as T. punctatum
sphenoides) only occurred in tropical
America and not in Florida. He further
determined that Trichomanes 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 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/
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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, 2013, https://
fnai.org/trackinglist.cfm) use the name
T. p. ssp. floridanum and indicate that
this subspecies’ taxonomic standing is
accepted. In summary, there is
consensus that Trichomanes punctatum
ssp. floridanum is a distinct taxon.
Currently there are two extant
metapopulations (a group of spatially
separated populations) of this
subspecies (Gann et al. 2002, pp. 552–
554), comprised of four populations in
Miami-Dade County and two in Sumter
County separated by a distance of
approximately 400 kilometers (km) (249
miles (mi)). Both extant
metapopulations residing in MiamiDade and Sumter Counties are
considered T. p. ssp. floridanum;
however, until recently, genetics
sampling had not been conducted
providing conclusive evidence that
these metapopulations are in fact the
same taxon. 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 well
known (Woodmansee 2013, pers.
comm.); the specific life history of
Trichomanes punctatum ssp.
floridanum, including information on
other members of the genus, is also
lacking. Like all ferns, this taxon has
two life-history stages, a gametophyte
stage and a sporophyte stage. However,
only the sporophyte form is
recognizable in the wild, as spores of
this plant are invisible to the naked eye
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(Possley 2013a, pers. comm.; van der
Heiden 2013b, pers. comm.).
All reported populations of
Trichomanes punctatum ssp.
floridanum have been in the sporophyte
stage. The initial stage, after a spore
germinates, is 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 typical form most ferns are observed
in. The sporophytes produce spores,
which in turn can germinate to produce
new gametophytes (Nelson 2000, pp.
17–19). Reproduction may also occur in
two other ways. Plants may reproduce
by division, when rhizomes (horizontal,
underground plant stems capable of
producing the shoot and root systems of
a new plant) break, forming clones of
the parent plant, or they may also
reproduce with the production of
gemmae (cells that detach from the
parent and develop into a new
individual) and propagules (a plant part
that becomes detached from the rest of
the plant and grows into a new plant)
produced by gametophytes, which can
grow into new gametophytes of the
same genotype (the genetic makeup of a
cell or individual) (Dassler and Farrar
2001, p. 354; Hill 2003, p. 12).
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 2013e,
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.
Recent field studies in Sumter County
on extant Trichomanes punctatum ssp.
floridanum populations found average
relative humidity to be around 95
percent, while ambient temperatures
were recorded to stay around 23 degrees
Celsius (°C) (73 degrees Fahrenheit (°F)).
However, during cooler periods (19–22
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°C; 66–70 °F) when humidity levels
dropped slightly (to around 92 percent
humidity), observed plant health
declined, demonstrating the fragile
nature of this taxon and its dependence
on high humid conditions (van der
Heiden and Johnson 2014, p. 9). 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.
Organizations such as the Institute for
Regional Conservation (IRC) and
Fairchild’s Center for Tropical Plant
Conservation (Fairchild) are working
together to understand the biology, life
history, and reproduction 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 has grown
14 separate clusters from plants
obtained in local hammocks (temperate
hardwood forests) and 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 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
underway 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 (Holst 2014,
pers. comm.).
Habitat
In southeastern North America,
Trichomanes spp. are considered rare
because of their delicate nature and
requirements for deeply sheltered
habitats with almost continuous high
moisture and humidity (Farrar 1993b,
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
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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 U.S. in
the State of Florida. In Florida, T. p. ssp.
floridanum is only known to occur in
Miami-Dade and Sumter Counties.
Both extant metapopulations live in
dense canopy habitats, with shady
conditions that may be obligatory due to
the poikilohydric (i.e., possess 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
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
epiphytic (a plant that grows nonparasitically upon another plant) or
epipetric (growing on rocks), typically
growing in rocky outcrops of rockland
hammocks, in oolitic (composed of
minute rounded concretions resembling
fish eggs) limestone solution holes, and,
occasionally, on tree roots in limestonesurrounded areas (Phillips 1940, p. 166;
Nauman 1986, p. 180; Whitney et al.
2004, pp. 105–106; Possley 2013f, pers.
comm.; van der Heiden 2014b, pers.
comm.). These rockland habitats are
outcrops primarily comprised of marine
limestone representing the distinct
geological formation of the Miami Rock
Ridge, a feature which 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 hammock (forest) on
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Fmt 4701
Sfmt 4702
61139
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 consist
of bare rock walls that 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 appearance of 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
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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). Plants live in a mesic hammock
on limestone boulders 0.1–1.5 m (0.3–
4.9 ft) tall (see ‘‘Current Range’’ section,
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, or 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).
Historically, mesic hammocks were
thought to be restricted to naturally fireprotected areas such as islands and
peninsulas of lakes.
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 64 percent (van der Heiden and
Johnson 2013, pp. 8, 20). 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 2013, p. 7).
Within one occupied Sumter County
hammock (Rocky Hammock), the
majority of Trichomanes punctatum
ssp. floridanum occur on the northern
face of limestone boulders; however,
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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). It has
been suggested the northern aspect of
limestone boulders are 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
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Fmt 4701
Sfmt 4702
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 comprised 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, pp. 7, 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). Recent field surveys
recorded 18 canopy species in Rocky
Hammock and 12 in Tree Frog
Hammock (van der Heiden and Johnson
2014, p. 19), both located in Sumter
County. 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.
Habitat differences between MiamiDade and Sumter Counties have enabled
this subspecies to adapt to very different
conditions at each location. In MiamiDade, where Trichomanes punctatum
ssp. floridanum currently is found, the
mean maximum temperature from the
last 10 years (2004–2013) was 29.0 °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
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for Sumter County with 23.4 °C (74.2°F)
recorded as the maximum temperature
for the last 10 years (2004–2013), and
11.8 °C (53.2°F) as the minimum
temperature for the same time period
(National Oceanic and Atmospheric
Administration 2014, https://
www1.ncdc.noaa.gov). Although it is
believed this subspecies needs high
temperatures and humidity, along with
dense canopy, the exact thresholds for
these variables have yet to be
determined.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
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, 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 (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%20bristle%20fern).
After the initial finding of
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
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19:10 Oct 08, 2014
Jkt 235001
present-day Castellow Hammock (Gann
2014d, pers. comm.). Additional
collections were obtained in 1903, in
Castellow Hammock by A.A. Eaton with
more recent observations by G. Gann
and K. Bradley in the late 1990s
(Bradley and Gann 1999), and J. Possley
and others (Gann et al. 2002, pp. 552–
554; Possley et al. 2013, pp. 43–45).
T. p. ssp. floridanum was collected in
Silver Palm Hammock in 1903, by A.A.
Eaton and later reported again in 1980;
however, this 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 destroyed, and what
remains is currently protected as a
Miami-Dade Conservation Area. 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/IRCSp
Account.asp?TXCODE=Tricpuncflor&
GENUS=Trichomanes&SPECIES=
punctatum&Author=Poir.&INFRA1=
subsp.&INFRA1NAME=ssp. floridanum
&INFRA1AUTHOR=Wess.%20Boer
&CommonNames=Florida%20bristle
%20fern. The last known collection in
Hattie Bauer Hammock was recorded in
1960, by
T. Darling, Jr., and subsequently
reported as extirpated by Gann et al.
(2002, pp. 552–554), until it was
rediscovered in this hammock in 2011
by 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 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).
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61141
Fuchs Hammock was also vouchered in
1993, following Hurricane Andrew
(1992) by A. Cressler (Cressler 12
February 1993, handwritten notes,), and
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,
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 2013j,
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 existing 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://regional
conservation.org/ircs/database/plants/
IRCSpAccount.asp?TXCODE=Tricpunc
flor&GENUS=Trichomanes&SPECIES=
punctatum&Author=Poir.&INFRA1=
subsp.&INFRA1NAME=ssp. floridanum
&INFRA1AUTHOR=Wess.%20Boer&
CommonNames=Florida%20bristle%20
fern) and a station presumably near the
Matheson Hammock Park vouchered by
G. Peterson in 1940.
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TABLE 1—SUMMARY OF HISTORICAL REPORTS, POPULATION LOCATIONS, AND CURRENT POPULATION AND HAMMOCK
STATUS OF TRICHOMANES PUNCTATUM SSP. FLORIDANUM IN MIAMI-DADE COUNTY, WHERE KNOWN
[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, j–k, 2014a–c; Possley 2013, 2014 pers. comm.; Gann
2013, pers. comm.; van der Heiden 2013e, pers. comm.; Gann 2014a–f, pers. comm.; Gann et al. 2014, https://regionalconservation.org/ircs/
database/plants/PlantPage.asp?TXCODE=Tricpuncflor]
Year(s) of
initial
report(s)
No.
Population location
1 ......
2 ......
Deering-Snapper Creek Hammock
(in R. Hardy Matheson Preserve).
Castellow Hammock .........................
3 ......
4 ......
Silver Palm Hammock ......................
Ross Hammock .................................
5 ......
Royal Palm Hammock (ENP); aka
Paradise Key.
Hattie Bauer Hammock (Orchid Jungle).
6 ......
Number of
specimens
collected
Observer
G.V. Nash .....
C.A. Mosier ...
J.J. Carter .....
.......................
.......................
J.J. Carter .....
3
1
2
4
1
2
Extirpated ...
1901
1915
1903
1903
1903
1906
J.K. Small,
J.K. Small,
J.K. Small,
A.A. Eaton
A.A. Eaton
J.K. Small,
1909
1917
1915
1915
1915
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 ........................
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 ...
2
None
2
3
5
7 ......
Shields Hammock .............................
1916
1934
1936
1940
1960
1915
8 ......
Nixon-Lewis Hammock .....................
1915
9 ......
Fuchs Hammock (Sykes Hammock)
1915
1954
1959
1969
10 ....
Addison Hammock (Deering Estate
at Cutler).
Matheson Hammock Park ................
Meissner Hammock ..........................
Cox Hammock (Monkey Jungle) ......
1916
J.K. Small, C.A. Mosier ...
L.J. Brass ........................
T. Darling Jr .....................
A.F. Clewell, F.C.
Craighead.
J.K. Small ........................
1940
1983
1989
G. Peterson .....................
G.N. Avery .......................
A. Cressler .......................
11 ....
12 ....
13 ....
Current
population
status
Extant .........
Extirpated ...
Extirpated ...
Current
hammock
status
Protected Area, Partially
Destroyed.
Protected Area.
Extirpated ...
Protected Area.
Protected Area, Partially
Destroyed.
Protected Area.
Extant .........
Protected Area.
1
2
2
1
1
1
Extirpated ...
Destroyed.
1
Extirpated ...
1
1
1
1
Extant .........
Protected Area, Partially
Destroyed.
Protected Area.
None
Unknown 1 ..
Protected Area.
2
None
None
Unknown 2 ..
Extant .........
Unknown 3 ..
Protected Area.
Protected Area.
Privately Owned, Partially
Destroyed.
1 Initial
report is questionable.
location of sample and associated report is questionable.
is not known whether the species still occurs here.
2 Precise
3 It
tkelley on DSK3SPTVN1PROD with PROPOSALS2
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
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19:10 Oct 08, 2014
Jkt 235001
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
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Fmt 4701
Sfmt 4702
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
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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 S.W.
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
61143
Garrett collected their specimens, which
is now extirpated.
TABLE 2—SUMMARY OF HISTORICAL REPORTS, POPULATION LOCATIONS, AND CURRENT POPULATION AND HAMMOCK
STATUS OF TRICHOMANES PUNCTATUM SSP. FLORIDANUM IN SUMTER COUNTY, WHERE KNOWN
[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. 2014, https://
regionalconservation.org/ircs/database/plants/PlantPage.asp?TXCODE=Tricpuncflor]
Year of
initial
report
Observer
Number of
specimens
collected
Current
population
status
1936
R.P. St. John ...................
1
Floral City Area 1 ...............................
Southeast of Floral City 1 ..................
1939
1954
J.B. McFarlin ...................
R. Garret ..........................
1
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) .........
1959
T. Darling Jr .....................
1
Presumed
Extirpated.
Unknown 2 ..
Presumed
Extirpated.
Unknown 2 ..
1963
O. Lakela .........................
1
Extirpated ...
1983
S.W. Leonard ..................
1
Extirpated ...
No.
Population location
1 ......
11.26 km (7 mi) East of Floral City 1
2 ......
3 ......
4 ......
5 ......
6 ......
Current
hammock
status
Privately Owned, Presumed Destroyed.
Unknown.
Privately Owned, Presumed Destroyed.
Privately Owned, Unknown.
Protected Area.
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).
tkelley on DSK3SPTVN1PROD with PROPOSALS2
Miami-Dade County
The four populations that constitute
the Miami-Dade County metapopulation
are located in urban preserves managed
by the County’s Environmentally
Endangered Lands (EEL) Program (see
Factor A, Conservation Efforts to Reduce
Habitat Destruction, Modification, or
Curtailment of Its Range, below). These
EEL properties 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
subpopulations in Fuchs Hammock
include a new population 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.
During 2011, another population was rediscovered at Hattie Bauer Hammock (8
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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. In general, Trichomanes
punctatum ssp. floridanum occurs in
small areas within each hammock.
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 2013f, 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 2013g, pers. comm.). A
plant sample was collected in NixonLewis 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; however, plants have
not been found there (Gann et al. 2009;
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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 (in ENP) for other rare plants
were also 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
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approximately 1,478 ha (3,652 ac) in
Sumter County. However, not all of
these areas have been systematically
surveyed. Although surveys conducted
of a boulder field within Withlacoochee
State Forest’s Jumper Creek Tract (called
the Indian Field Ledges) in August 2007
and April 2013 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.).
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 (WSF) 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
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.
TABLE 3—SUMMARY OF KNOWN EXTANT OCCURRENCES OF Trichomanes punctatum SSP. floridanum. (POSSLEY 2013,
P. 1–2; DOZIER 2014, PERS. COMM.; VAN DER HEIDEN AND JOHNSON 2014, PP. 1–3).
Metapopulation
location (County)
Population location
Land ownership
Miami-Dade .................................
Miami-Dade .................................
Miami-Dade .................................
Miami-Dade .................................
Sumter .........................................
Meissner Hammock ...............................................
Fuchs .....................................................................
Castellow ...............................................................
Hattie Bauer ...........................................................
Rocky Hammock, Withlacoochee State Forest’s
Jumper Creek Tract.
Tree Frog Hammock, Withlacoochee State Forest’s Jumper Creek Tract.
State ..............................
County ...........................
County ...........................
County ...........................
State ..............................
2
4
3
1
1
Extant.
Extant.
Extant.
Extant.
Extant.
State ..............................
1
Extant.
Sumter .........................................
Population Estimates and Status
Trichomanes punctatum ssp.
floridanum grows in dense mats and is
rhizomatous (a horizontal stem that
often sends out roots and shoots 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
Number of
subpopulations
Status
subpopulations (i.e., nine solution holes
and one rocky outcropping). 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
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 covered
(m2)
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Metapopulation
Population
Subpopulation
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade ................................
Miami-Dade County Total ...
Sumter ........................................
Sumter ........................................
Hattie Bauer Hammock ......................................
Fuchs Hammock ................................................
Fuchs Hammock ................................................
Fuchs Hammock ................................................
Fuchs Hammock ................................................
Meissner Hammock ...........................................
Meissner Hammock ...........................................
Castellow Hammock ..........................................
Castellow Hammock ..........................................
Castellow Hammock ..........................................
.............................................................................
Rocky Hammock ................................................
Tree Frog Hammock ..........................................
Hole (no tag) ................
Hole 532 ......................
Hole 533 ......................
Hole 1431 ....................
Root 1430 ....................
Hole 2319 ....................
Hole 3337 ....................
Hole 2332 ....................
Hole 2331 ....................
Hole 944 ......................
......................................
N/A ...............................
N/A ...............................
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0.078
0.017
0.038
0.128
0.047
0.145
0.713
4.688
3.925
0.141
9.920
4.355
0.132
09OCP2
............
............
............
............
............
............
............
............
............
............
m2 ......
............
............
Number of
clusters
2–10
2–10
2–10
2–10
1
2–10
2–10
11–100
11–100
2–10
............................
44
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61145
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)—Continued
Population
Subpopulation
Estimated
area covered
(m2)
Number of
clusters
Sumter County Total ...........
.............................................................................
......................................
4.487 m2 ......
............................
Total Area Covered .............
.............................................................................
......................................
14.407 m2 ....
............................
Metapopulation
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 2013h, 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
July 2013, totaling an area of 0.230 m2
(2.476 ft2) (Possley 2013, pp. 1–2;
Possley et al. 2013, pp. 43–45).
tkelley on DSK3SPTVN1PROD with PROPOSALS2
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.
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
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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. Each of these factors as
applied to Trichomanes punctatum ssp.
floridanum is discussed below.
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 the
species responds negatively, the factor
may be a threat, and we then attempt to
determine if that factor rises to the level
of 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
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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
found have 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, https://
www.fnai.org/PDF/NC/Rockland_
Hammock_Final_2010.pdf). 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,
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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 destroyed Ross Hammock (Phillips
1940, p. 167).
Rockland hammock habitat is now
limited to public conservation lands
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).
Due to the possibility that additional
populations of Trichomanes punctatum
ssp. floridanum may be found on
private property and could be
destroyed, and the fact that there are no
guarantees that the limited rockland
hammock habitat will remain as public
conservation land in perpetuity, 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
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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 and in
existing conservation areas.
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.). Although undeveloped land is
more abundant in Sumter County than
in Miami-Dade County, the fact that no
virgin land remains within Sumter
County may reduce the likelihood of
new populations being discovered
(Farnsworth 2013, 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 and within existing conservation
areas, habitat loss due to human
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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 extirpation
and decline of this metapopulation
(Nauman 1986, p. 182; see also
‘‘Historical Range/Distribution’’, MiamiDade 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 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 for 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
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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, it
is possible in the future. Minimum
flows and levels (MFLs), which are
water withdrawal standards to limit
water use set the by regional Water
Management Districts (WMDs), 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 table
use, it is believed 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
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.
As a hygrophilous (living or growing
in damp places) subspecies thought to
be restricted to a consistent humid
¨
microhabitat (Kromer and Kessler 2006,
p. 57), high humidity is a critical factor
to its survival; any habitat modification
or destruction that changes ambient
humidity levels is believed to be 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
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2013f, pers. comm.). Van der Heiden
and Johnson (2013, 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 is also 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
avoid desiccation from excessive light
exposure (van der Heiden 2013c, pers.
comm.; Possley 2013f, pers. comm.;
Adimey 2013a-b, field notes). Currently,
in both metapopulations, dense canopy
cover is a necessity; however, the lower
limits of canopy density needed to
ensure survival are 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 2013h, 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, canopy loss is believed to be
a limiting factor for the future
persistence of the subspecies and is
therefore considered a threat to T. p.
spp. floridanum.
Habitat Fragmentation
Habitat fragmentation limits dispersal
and population size, and promotes
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61147
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,
fragmented 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,
thorough knowledge of the impacts and
subsequent consequences from habitat
fragmentation is unknown for both
metapopulations of Trichomanes
punctatum ssp. floridanum because
information and understanding of
dispersal mechanisms for this
subspecies is currently lacking. The best
available data regarding the impacts of
habitat fragmentation on other plant
species suggests 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 in which both
metapopulations occur. All known
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 (https://www.miamidade.gov/
environment/endangered-lands.asp).
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 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
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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 owned by the Miami-Dade
County Parks, Recreation and Open
Spaces 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). A precursor to the EEL
Program is the EEL Covenant Program,
which regulates private lands for
conservation through easements.
EEL Covenant Program
In 1979, Miami-Dade County enacted
the EEL Covenant Program, which
reduces taxes for private landowners of
natural forest communities (NFC) such
as pine rocklands and rockland
hammocks. Under the EEL Covenant
Program, landowners agree not to
develop their property and 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 regulates
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 hammocks
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).
These County- and State-owned land
areas are critical to protecting
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
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in Miami’s EEL Preserves have been
underway for many years. In MiamiDade County, conservation lands are
and have been monitored by Fairchild
and IRC, in coordination with the EEL
Program, to assess habitat status and
determine any changes that may pose a
threat to or alter the abundance of T. p.
ssp. floridanum (Possley 2013m, 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.
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 without further
explanation (Gann 2013, https://regional
conservation.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). This is not surprising since
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
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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. floridanum was found
in an additional nine hammocks in
Miami-Dade County. These populations
have been extirpated, and the historical
range of the southern metapopulation
has been reduced by nearly 80 percent.
Although much of the habitat has been
destroyed and 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. floridanum currently
exists are still vulnerable to activities in
the surrounding areas including
agricultural clearing and hydrologic
alterations.
The Sumter County metapopulation
of Trichomanes puctatum ssp.
floridanum is composed of two known
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
continues to be a threat to T. p.
floridanum populations and habitat.
Although historical habitat modification
and destruction in Sumter County has
not been as extensive as in South
Florida, this is a future potential threat
due to the large areas of undeveloped
lands within Sumter County.
The destruction and modification of
habitats 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 puctatum ssp.
floridanum’s survival; therefore, any
habitat modification or destruction that
changes ambient humidity levels or
canopy cover poses a threat to this
subspecies. Thorough knowledge of the
impacts of habitat fragmentation is
unknown for both metapopulations of T.
p. ssp. floridanum because information
on dispersal mechanisms of this
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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. Water
withdrawals may still be of some
concern; however, the impact of this
factor is not currently known, and
therefore, we have determined it to be
a stressor, but it is not rising to the level
of a threat at this time.
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 puctatum 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 a threat to
Trichomanes punctatum ssp.
floridanum.
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Factor C. Disease or Predation
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 to determine
whether they effectively reduce or
remove threats to Trichomanes
punctatum ssp. floridanum.
Federal
The only known extant populations of
Trichomanes punctatum ssp.
floridanum occur on State- or Countyowned properties and development of
these areas will likely require no
Federal permit or other authorization.
Therefore, projects that affect T. p. ssp.
floridanum on State- and County-owned
lands do not have a Federal oversight,
such as complying with the National
Environmental Policy Act (NEPA) (42
U.S.C. 4321 et seq.), unless the project
has a Federal nexus (Federal funding,
permits, or other authorizations).
Therefore, T. p. ssp. floridanum has no
direct Federal regulatory protection in
its known occupied habitats.
No diseases or incidences of
predation have been reported for
State
Trichomanes punctatum ssp.
floridanum. Therefore, the best available
FNAI considers the State status of
data do not indicate that disease or
Trichomanes punctatum ssp.
predation is a threat to the subspecies.
floridanum to be S1, ‘‘critically
imperiled in Florida because of extreme
Factor D. The Inadequacy of Existing
rarity (five or fewer occurrences or less
Regulatory Mechanisms
than 1,000 individuals) or because of
Under this factor, we examine
extreme vulnerability to extinction due
whether threats to the subspecies
to some natural or man-made factor’’
discussed under the other factors are
(FNAI 2013, https://fnai.org/PDF/
continuing due to an inadequacy of an
Element_tracking_summary_
existing regulatory mechanism. Section
current.pdf). The IRC considers its
4(b)(1)(A) of the Act requires the Service status as ‘‘critically imperiled’’ (Gann et
to take into account ‘‘those efforts, if
al. 2002, pp. 552–554).
The Florida Department of
any, being made by any State or foreign
Agriculture and Consumer Services
nation, or any political subdivision of a
(FDACS) has listed Trichomanes
State or foreign nation, to protect such
punctatum ssp. floridanum on the
species. . . .’’ In relation to Factor D
Regulated Plant Index (Index) as
under the Act, we interpret this
endangered under Chapter 5B–40,
language to require the Service to
Florida Administrative Code (State of
consider relevant Federal, State, and
Florida 2013, Florida Statutes: https://
tribal laws, regulations, and other such
www.flrules.org/gateway/
mechanisms that may minimize any of
RuleNo.asp?title=PRESERVATION
the threats we describe in threat
analyses under the other four factors, or %20OF%20NATIVE%
20FLORA%20OF%20FLORIDA&ID=5B–
otherwise enhance conservation of the
40.0055). This listing provides little or
species. We give strongest weight to
no habitat protection beyond the State’s
statutes and their implementing
Development of Regional Impact
regulations and to management
direction that stems from those laws and process, which discloses impacts from
regulations. An example would be State projects, but provides no regulatory
protection for State-listed plants on
governmental actions enforced under a
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61149
private lands. Florida Statutes 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. Subsections (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, https://
www.leg.state.fl.us/Statutes/
index.cfm?Mode=View%20Statutes&
Submenu=1&Tab=statutes). 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 there is no imminent threat to
Withlacoochee State Forest being
modified (e.g., logged), altered (e.g.,
installation of pipelines), or sold for
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development, the State may be allowed
to proceed with such actions only after
they have been reviewed and approved
at public meetings by the Acquisition
and Restoration Council (ARC) and,
depending upon the issue, by the Board
of Trustees of the Internal Improvement
Trust Fund of the State of Florida.
Although the MFLs established by the
South Florida Water Management
District (SFWMD) in southeast Florida
(a separate entity than the Southwest
Florida Water Management District
(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 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.
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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 onehalf an acre can be cleared if the request
is deemed a reasonable use of property;
this allowance oftentimes 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, RER pursues unpermitted
work through appropriate enforcement
action and seeks restoration 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 on
a parcel in limited circumstances for
parcels less than 2.02 ha (5 ac) in size
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and only requires coordination with the
landowner 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
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 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. Any undocumented
occurrences of T. p. ssp. floridanum and
suitable habitat on private lands are at
risk. 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, there is still a significant
portion of the hammock that 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. The
landowner could apply for a permit and
destroy undocumented populations of
T. p. ssp. floridanum and the
subspecies’ habitat on this site. Because
the site is private and not managed as
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a preserve (i.e., it is not controlled for
nonnative, invasive plant species),
degradation of potential habitat for T. p.
ssp. floridanum is likely. Furthermore, a
change in ownership, accompanied by
subsequent modifications in land-use,
may cause extirpation of any
undocumented T. p. ssp. floridanum
populations or negatively impact
suitable habitat. Additionally, MiamiDade 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.).
Because a comprehensive survey in
Sumter County has not yet been
conducted, there is a chance of finding
new populations of Trichomanes
punctatum ssp. floridanum in the area.
Any undocumented occurrences and
suitable habitat that could be important
for reintroduction or recolonization of
this subspecies in Sumter County,
especially on private lands, are
potentially at risk due to development.
Under section 13–644(a)(1) of the
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, County code prevents
unmitigated destruction of endangered,
threatened, or rare species only when
associated with ‘‘major developments.’’
However, these sections do not prevent
land destruction or development on
private land where any undocumented
populations of T. p. ssp. floridanum or
suitable habitat for future reintroduction
are vulnerable. 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.
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Summary of Factor D
Currently, Trichomanes punctatum
ssp. floridanum is found only on State
and County lands; however, there is no
regulatory mechanism in place that
provides 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 (nonwetlands) 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 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 are discussed in
detail below.
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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,
promoting overshading and forming
dense strata (layers) in hammocks,
which alter the habitat and its
surrounding conditions (Possley 2013f,
pers. comm.). It has also been suggested
that the insular nature of south Florida,
as well as the hammocks themselves,
predispose this habitat to 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, as
management in these areas generally
does not protect native species and
ecological processes, as intended.
Problematic nonnative invasive plants
in Miami-Dade County associated with
Trichomanes punctatum ssp.
floridanum include Schinus
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terebinthifolius (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 2013h-i, 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
2014, 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 and removing the
nonnative species exposes the fern. In
the case of Castellow Hammock, the
majority of the shade near two of the
large solution holes containing
Trichomanes punctatum ssp.
floridanum is provided by giant Schinus
terebinthifolius 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. terebinthifolius
canopy has already occurred. In this
case, the subpopulation of T. p. ssp.
floridanum below where the S.
terebinthifolius tree was turned brown;
however, T. p. ssp. floridanum could
eventually revitalize if sufficient canopy
is re-established to limit sunlight
exposure (Possley 2013e, pers. comm.).
Additionally, nonnative plant control
may also become a threat when T. p.
ssp. floridanum are inadvertently
sprayed while conducting local
nonnative removal efforts (Possley
2013e, pers. comm.).
Nonnative plant species are also a
concern on private lands, where often
these species are not controlled due to
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associated costs, lack of interest, or lack
of knowledge of detrimental impacts to
the ecosystem. Undiscovered
populations of Trichomanes punctatum
ssp. floridanum on private lands could
certainly be at risk. 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 laying against
or rubbing their bodies against large
rocks, removing existing vegetation in
the process. Recently, van der Heiden
and Johnson (2013, 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
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 Liguus
(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 be 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
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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
Intergovernmental Panel on Climate
Change (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, pp. 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
(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
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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
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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 groundwater 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
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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 in 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 which extends from the top of the
ground surface to the water table);
increase salinity in the bottom portion
of the freshwater lens, thereby
increasing brackishness of plantavailable water; and influence tree
species composition of coastal
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
such as Trichomanes punctatum ssp.
floridanum. Shifts in freshwater flows,
annual precipitation, and variability in
SLR can impact salinity regimes.
Although it is unknown if salinity
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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, this 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
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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,
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
exogenous stresses can improve
resiliency 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 resilience,
population growth, and potential for
natural dispersal, and controlling for
nonnative species. Efforts to actively
manage for resilience are currently
limited for both metapopulations of T.
p. ssp. floridanum due to logistic
feasibility, 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 large 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 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
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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 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
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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.
Environmental Stochasticity
Endemic species whose populations
exhibit a high degree of isolation, such
as Trichomanes punctatum ssp.
floridanum, are extremely susceptible 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 and environmental
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 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 one
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
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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 hurricane and tropical
storm frequencies in the Atlantic are
expected to decrease between 10–30
percent by 2100 (Knutson et al. 2008,
pp. 1–21). For those models that predict
fewer hurricanes, predictions of
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
hammocks 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 believed to
be the threat with greatest impact to
existing metapopulations of
Trichomanes punctatum ssp.
floridanum (Adimey 2013b, field notes;
Possley 2013p, pers. comm.). For
example, impacts from Hurricane
Andrew in 1992 were thought to be
responsible for the temporary loss of
this subspecies from Hattie Bauer
Hammock, where it had been observed
for many years. Following this
hurricane, the canopy was destroyed,
allowing increased exposure to sunlight
for several years. T. p. ssp. floridanum
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was not seen again in Hattie Bauer
Hammock until 2011 (Possley 2013p,
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
original 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 small
population size, 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
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. Multi-year droughts may
negatively impact populations. While
droughts are natural events, they are a
threat because there are so few
populations of this subspecies. Specific
range requirements regarding humidity,
temperature, and precipitation 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
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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, its genetic variability
and overall resilience is likely low.
These factors, combined with additional
stress from habitat modifications (e.g.,
hydrological changes) may increase the
inherent risk of 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 as addressed above are
a threat to the persistence of this
subspecies in the future (Adimey 2013b,
field notes; Possley 2013p, 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
influenced the occurrence of fire;
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 (1916, https://
www.floridamemory.com/items/show/
49132; 1917, https://
www.floridamemory.com/items/show/
49465). 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.
Generally, hammock environments
are considered less susceptible to
wildfires because their shaded, humid
microclimate is not conducive to fire
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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 (Werner 2013d, pers.
comm; Possley 2013l, pers. comm.).
Snyder (et al. 1990, p. 238) points out
that the high organic content of
hammock soils in south Florida can
enable it to burn; however, soil fires
typically only burn in hammocks in
times of drought or when they 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, the
natural fire-resistant features of these
two habitats, and, in Sumter County,
hydric hammock surrounding
Trichomanes punctatum ssp.
floridanum populations. However,
under future projected climate change
scenarios, we expect drought conditions
to exacerbate the effects on T. p. ssp.
floridanum to a level at which fire
becomes a threat in the future.
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 2013h, 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
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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 does not appear to be
occurring at this time, and we have
determined it does not pose a threat to
T. p. ssp. floridanum.
Small Population Size and Isolation
Low population resilience is a serious
concern for species that are restricted to
geographically limited areas, as they are
inherently more vulnerable to extinction
than widespread species due to an
increased risk of genetic bottlenecks,
random demographic fluctuations,
climate change, and localized
catastrophes such as hurricanes and
disease outbreaks (Mangel and Tier
1994, p. 607; Pimm et al. 1988, p. 757).
These problems are further magnified
when populations are few, populations
are restricted to very small geographic
areas, and numbers of individuals are
limited, as in the case of Trichomanes
punctatum ssp. floridanum. 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 is also a
stressor that contributes to the low
population resilience for this subspecies
(see ‘‘Habitat Fragmentation’’ under
Factor A).
Limited genetic variability will also
impact population resilience. The
ability of populations 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,
with few plants, the genetic variability
is considered low, and the subspecies is
inherently at risk due to stochastic
events and changes in environmental
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conditions (Matthies et al. 2004, pp.
481–488).
In summary, population resilience 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 low
population resilience to Trichomanes
punctatum ssp. floridanum that could
arise due to small population size, 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
extinction from one location would
occur.
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
manager for further attention (Possley
2013p, pers. comm.). IRC also conducts
research and monitoring in various
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
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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. This is especially alarming
since droughts, tropical storms, and
hurricanes are common occurrences in
Florida. 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 cause 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
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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.
Proposed Determination
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 (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.
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
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
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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, are isolated, and
have limited to no potential 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
in light of the fact these events cannot
be controlled and mitigation measures
have yet to be addressed. Individually
and collectively, all 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 propose to list
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
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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 ongoing, and
are expected to continue into the future.
Under the Act and our implementing
regulations, a species may warrant
listing if it is endangered or threatened
throughout all or a significant portion of
its range. The threats to the survival of
Trichomanes punctatum ssp.
floridanum occur throughout the
subspecies’ range and are not restricted
to any particular significant portion of
that range. Accordingly, our assessment
and proposed determination applies to
the subspecies throughout its entire
range.
Significant Portion of the 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 Service’s SPR Policy
(79 FR 37578, July 1, 2014).
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness and conservation by
Federal, State, 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 to threatened) 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. If we list
Trichomanes punctatum ssp.
floridanum, when completed, the draft
and final recovery plans would 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.
If this subspecies is listed, funding for
recovery actions would 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 would 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
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to aid species recovery can be found at:
https://www.fws.gov/grants.
Although Trichomanes punctatum
ssp. floridanum is only proposed for
listing under the Act at this time, please
let us know if you are interested in
participating in conservation efforts for
this species. Additionally, we invite you
to submit any new information on this
species whenever it becomes available
and any information you may have for
conservation planning purposes (see
FOR FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as 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)(4) of the Act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2) of
the Act requires Federal agencies to
ensure that activities they authorize,
fund, or carry out are not likely to
jeopardize the continued existence of
the species or destroy or adversely
modify its critical habitat. If a Federal
action may affect a listed species or its
critical habitat, the responsible Federal
agency must enter into consultation
with the Service.
Federal agency actions within the
subspecies’ 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 and any other landscapealtering activities.
With respect to endangered plants,
prohibitions outlined at 50 CFR 17.61
make it illegal for any person subject to
the jurisdiction of the United States to
import or export, transport in interstate
or foreign commerce in the course of a
commercial activity, sell or offer for sale
in interstate or foreign commerce, or 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
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law. Exceptions to these prohibitions
are outlined 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 proposed listing on
proposed and ongoing activities within
the range of the species proposed for
listing. If we list Trichomanes
punctatum ssp. floridanum, 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.
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61159
At this time, we are unable to identify
specific activities that would not be
considered to result in a violation of
section 9 of the Act because
Trichomanes punctatum ssp.
floridanum occurs in a variety of habitat
conditions across its range and it is
likely that site-specific conservation
measures may be needed for activities
that may directly or indirectly affect the
subspecies.
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.’’
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.
As discussed in the Factor B analysis
(see above), there is currently no
imminent threat of take attributed to
collection or vandalism for this species,
and identification and mapping of
critical habitat is not expected to initiate
any such threat. Therefore, in the
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absence of finding that the designation
of critical habitat would increase threats
to a species, if there are any benefits to
a critical habitat designation, a finding
that designation is prudent is warranted.
Here, the potential benefits of
designation include: (1) Triggering
consultation under section 7 of the Act,
in new areas for actions in which there
may be a Federal nexus where it would
not otherwise occur because, for
example, it is unoccupied; (2) focusing
conservation activities on the most
essential features and areas; (3)
providing educational benefits to State
or county governments or private
entities; and (4) preventing people from
causing inadvertent harm to the species.
Because we have 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 determine that
designation of critical habitat is prudent
for Trichomanes punctatum ssp.
floridanum.
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
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.
Our regulations at 50 CFR 424.19
require the Service to ‘‘make available
for public comment the draft economic
analysis of the designation’’ at the time
the proposed critical habitat rule is
published in the Federal Register. At
this point, a careful assessment of the
economic impacts that may occur due to
a critical habitat designation is still
ongoing, and we are still in the process
of acquiring the information needed to
perform this assessment. Accordingly,
we find designation of critical habitat
for Trichomanes punctatum ssp.
floridanum to be not determinable at
this time.
Required Determinations
tkelley on DSK3SPTVN1PROD with PROPOSALS2
Clarity of the Rule
We are required by Executive Orders
12866 and 12988 and by the
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Presidential Memorandum of June 1,
1998, to write all rules in plain
language. This means that each rule we
publish must:
(1) Be logically organized;
(2) Use the active voice to address
readers directly;
(3) Use clear language rather than
jargon;
(4) Be divided into short sections and
sentences; and
(5) Use lists and tables wherever
possible.
If you feel that we have not met these
requirements, send us comments by one
of the methods listed in the ADDRESSES
section. To better help us revise the
rule, your comments should be as
specific as possible. For example, you
should tell us the numbers of the
sections or paragraphs that are unclearly
written, which sections or sentences are
too long, the sections where you feel
lists or tables would be useful, etc.
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 need
not be prepared in connection with
listing a species as an endangered or
threatened species under the 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
Frm 00026
Fmt 4701
Sfmt 4702
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 proposed
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.
Proposed Regulation Promulgation
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
50 of the Code of Federal Regulations,
as set forth below:
PART 17—[AMENDED]
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
PO 00000
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.
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245, 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) * * *
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*
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Federal Register / Vol. 79, No. 196 / Thursday, October 9, 2014 / Proposed Rules
Species
Historic range
Scientific
name
*
FERNS AND ALLIES
*
Trichomanes
punctatum ssp.
floridanum.
*
*
*
*
Florida bristle fern ..
*
*
*
*
Family
Status
When listed
Common name
*
*
*
U.S.A. (FL) .............
*
*
*
*
*
E
*
*
*
Hymenophyllaceae
*
[FR Doc. 2014–23686 Filed 10–8–14; 8:45 am]
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BILLING CODE 4310–55–P
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Special
rules
*
*
NA
Dated: September 26, 2014.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife
Service.
*
Critical
habitat
09OCP2
NA.
*
Agencies
[Federal Register Volume 79, Number 196 (Thursday, October 9, 2014)]
[Proposed Rules]
[Pages 61135-61161]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-23686]
[[Page 61135]]
Vol. 79
Thursday,
No. 196
October 9, 2014
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); Proposed Rules
Federal Register / Vol. 79 , No. 196 / Thursday, October 9, 2014 /
Proposed Rules
[[Page 61136]]
-----------------------------------------------------------------------
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: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service, propose to list
Trichomanes punctatum ssp. floridanum (Florida bristle fern), a plant
subspecies from Miami-Dade and Sumter Counties in Florida, as an
endangered species under the Endangered Species Act of 1973, as amended
(Act). If we finalize this rule as proposed, it would extend the Act's
protections to this plant and add this plant to the Federal List of
Endangered and Threatened Plants.
DATES: We will accept comments received or postmarked on or before
December 8, 2014. Comments submitted electronically using the Federal
eRulemaking Portal (see ADDRESSES below) must be received by 11:59 p.m.
Eastern Time on the closing date. We must receive requests for public
hearings, in writing, at the address shown in FOR FURTHER INFORMATION
CONTACT by November 24, 2014.
ADDRESSES: You may submit comments by one of the following methods:
(1) Electronically: Go to the Federal eRulemaking Portal: https://www.regulations.gov. In the Search box, enter FWS-R4-ES-2014-0044,
which is the docket number for this rulemaking. Then, in the Search
panel on the left side of the screen, under the Document Type heading,
click on the Proposed Rules link to locate this document. You may
submit a comment by clicking on ``Comment Now!''
(2) By hard copy: Submit by U.S. mail to: Public Comments
Processing, Attn: FWS-R4-ES-2014-0044; Division of Policy and
Directives Management; U.S. Fish and Wildlife Service, MS: BPHC, 5275
Leesburg Pike, Falls Church, VA 22041-3803.
We request that you send comments only by the methods described
above. We will post all comments on https://www.regulations.gov. This
generally means that we will post any personal information you provide
us (see Information Requested, below, for more information).
FOR FURTHER INFORMATION CONTACT: Craig Aubrey, 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 Endangered Species Act
(Act), if we find that a species warrants listing as an endangered or
threatened species throughout all or a significant portion of its
range, we are required to promptly publish a proposal in the Federal
Register and make a determination on our proposal within 1 year.
Listing a species as an endangered or threatened species can only be
completed by issuing a rule. In the near future, we intend to propose
to designate critical habitat for Trichomanes punctatum ssp. floridanum
under the Act. Critical habitat is prudent, but not determinable at
this time. We will publish a proposal to designate critical habitat for
Trichomanes punctatum ssp. floridanum under the Act in the near future.
This rule proposes to list Trichomanes punctatum ssp. floridanum
(Florida bristle fern) as an endangered species.
The basis for our action. Under the Act, we may 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 resulting in changes in canopy, humidity,
hydrology, and fragmentation (Factor A); and 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).
We will seek peer review. We will seek comments from independent
specialists to ensure that our determination is based on scientifically
sound data, assumptions, and analyses. We will invite these peer
reviewers to comment on our listing proposal. Because we will consider
all comments and information we receive during the comment period, our
final determination may differ from this proposal.
Information Requested
Public Comments
We intend that any final action resulting from this proposed rule
will be based on the best scientific and commercial data available and
be as accurate and as effective as possible. Therefore, we request
comments or information from other concerned governmental agencies,
Native American tribes, the scientific community, industry, or any
other interested parties concerning this proposed rule. We particularly
seek comments concerning:
(1) Trichomanes punctatum ssp. floridanum's biology, range, and
population trends, including:
(a) Biological or ecological requirements of the plant, including
habitat requirements;
(b) Genetics and taxonomy;
(c) Historical and current range, including distribution patterns;
(d) Historical and current population levels, and current and
projected trends; and
(e) Past and ongoing conservation measures for the plant, its
habitat, or both.
(2) Factors that may affect the continued existence of the plant,
which may include habitat modification or destruction, overutilization,
disease, predation, the inadequacy of existing regulatory mechanisms,
or other natural or manmade factors.
(3) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to this plant and existing regulations
that may be addressing those threats.
(4) Additional information concerning the historical and current
status, range, distribution, and population size of this plant,
including the locations of any additional populations of the plant.
Please include sufficient information with your submission (such as
scientific journal articles or other publications) to allow us to
verify any scientific or commercial information you include.
Please note that submissions merely stating support for or
opposition to the action under consideration without providing
supporting information, although noted, will not be considered in
making a determination, as section
[[Page 61137]]
4(b)(1)(A) of the Act (16 U.S.C. 1531 et seq.) directs that
determinations as to whether any species is an endangered or threatened
species must be made ``solely on the basis of the best scientific and
commercial data available.''
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in the ADDRESSES section. We request
that you send comments only by the methods described in the ADDRESSES
section.
If you submit information via https://www.regulations.gov, your
entire submission--including any personal identifying information--will
be posted on the Web site. If your submission is made via a hardcopy
that includes personal identifying information, you may request at the
top of your document that we withhold this information from public
review. However, we cannot guarantee that we will be able to do so. We
will post all hardcopy submissions on https://www.regulations.gov.
Comments and materials we receive, as well as supporting
documentation we used in preparing this proposed rule, will be
available for public inspection on https://www.regulations.gov, or by
appointment, during normal business hours, at the U.S. Fish and
Wildlife Service, South Florida Ecological Services Office (see FOR
FURTHER INFORMATION CONTACT).
Public Hearing
Section 4(b)(5) of the Act provides for one or more public hearings
on this proposal, if requested. Requests must be received within 45
days after the date of publication of this proposed rule in the Federal
Register. Such requests must be sent to the address shown in the FOR
FURTHER INFORMATION CONTACT section. We will schedule public hearings
on this proposal, if any are requested, and announce the dates, times,
and places of those hearings, as well as how to obtain reasonable
accommodations, in the Federal Register and local newspapers at least
15 days before the hearing.
Peer Review
In accordance with our joint policy on peer review published in the
Federal Register on July 1, 1994 (59 FR 34270), during the public
comment period we will seek the expert opinions of appropriate and
independent specialists regarding this proposed rule. The purpose of
peer review is to ensure that our proposed listing determination is
based on scientifically sound data, assumptions, and analyses. The peer
reviewers will have expertise in Trichomanes punctatum ssp.
floridanum's biology, habitat, and physical or biological factors.
Previous Federal Actions
Trichomanes punctatum ssp. floridanum was first recognized as a
candidate for possible future listing on November 9, 2009 (74 FR
57804), and we assigned the subspecies a listing priority number (LPN)
of 3. Candidate species are assigned LPNs based on immediacy and
magnitude of threats, as well as taxonomic status. The lower the LPN,
the higher priority that species is for us to determine appropriate
action using our available resources (September 21, 1983; 48 FR 43098).
An LPN of 3 is the lowest LPN appropriate for a subspecies such as this
fern, indicating that it is a high priority for the U.S. Fish and
Wildlife Service (Service) to determine appropriate action. T. p. ssp.
floridanum has remained on the candidate list with an LPN of 3 since
2009 (see 78 FR 70104, November 22, 2013; 77 FR 69994, November 21,
2012; 76 FR 66370, October 26, 2011; 75 FR 69222, November 10, 2010; 74
FR 57804, November 9, 2009).
On May 10, 2011, the Service announced a workplan to restore
biological priorities and certainty to the listing process. As part of
an agreement with the Center for Biological Diversity and WildEarth
Guardians, we filed the workplan with the U.S. District Court for the
District of Columbia. The workplan will enable the agency, over a
period of 6 years, to systematically review and address the needs of
more than 250 species, including Trichomanes punctatum ssp. floridanum,
that were identified in our November 10, 2010, candidate notice of
review (CNOR), published in the Federal Register at 75 FR 69222, ssp.
floridanum to determine if these species should be added to the Federal
Lists of Endangered and Threatened Wildlife and Plants. This workplan
will enable the Service to again prioritize its workload based on the
needs of candidate species, while also providing State wildlife
agencies, stakeholders, and other partners clarity and certainty about
when listing determinations will be made. On July 12, 2011, the Service
reached an agreement with another plaintiff group and further
strengthened the workplan, which will allow the agency to focus its
resources on the species most in need of protection under the Act.
These agreements were approved by the court on September 9, 2011. We
are making this proposed listing determination for Trichomanes
punctatum ssp. floridanum now as part of the court-approved workplan.
Background
It is our intent to discuss below only those topics directly
relevant to the listing of Trichomanes punctatum ssp. floridanum as an
endangered species in this proposed rule.
Species Description
Trichomanes punctatum ssp. floridanum, commonly referred to as the
Florida bristle fern, is mat-forming, has no roots, and contains
trichomes (hairlike/bristlelike outgrowths) on the tip of the fern
(Wunderlin and Hansen 2000, pp. 153-154). This subspecies is very small
in size and superficially resembles other bryophytes, such as mosses
and liverworts, making it difficult to observe in its natural habitat.
T. p. ssp. floridanum has thin veinlets (small veins) that are not
enlarged towards the margin while veins are uniform in width to their
apices (tips) (Nauman 1986, p. 179); fronds (leaves of ferns) are
considered simple (Morton 1963, p. 89).
Wunderlin and Hansen (2000, pp. 153-154) described Trichomanes
punctatum ssp. floridanum as having separated 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.
This subspecies has few false veins, and its true veins are not
enlarged at their apex.
One unique characteristic of this plant is that it lacks cuticles
(the protective layer that cover the epidermis, which is the outermost
layer of cells that cover the leaves) or has highly reduced cuticles,
and has differentiated epidermises and stomata (small openings in
leaves and stems through which gases are exchanged), causing dependence
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 spp. to shaded areas
with high humid forested environments, 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 generally lack ecological
information (Nauman 1986, p. 179; Nelson 2000, p. 77). The genus
belongs to the family
[[Page 61138]]
Hymenophyllaceae and the hymenophylloid clade, where ferns are also
referred to as filmy ferns, which represents the thin, filmy leaves of
the species (Nelson 2000, p. 77). The common name, bristle fern, is
used to reference the bristlelike structure that protrudes from the
mature sporangia (a structure that holds and produces spores) (Nelson
2000, p. 77).
Five species commonly known as bristle ferns (Trichomanes spp.)
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 plants in Florida
represented the same taxon, not two separate species, and that T.
sphenoides (which he described as T. punctatum sphenoides) only
occurred in tropical America and not in Florida. He further determined
that Trichomanes 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 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, 2013, https://fnai.org/trackinglist.cfm) use the name T. p. ssp. floridanum and indicate that
this subspecies' taxonomic standing is accepted. In summary, there is
consensus that Trichomanes punctatum ssp. floridanum is a distinct
taxon.
Currently there are two extant metapopulations (a group of
spatially separated populations) of this subspecies (Gann et al. 2002,
pp. 552-554), comprised of four populations in Miami-Dade County and
two in Sumter County separated by a distance of approximately 400
kilometers (km) (249 miles (mi)). Both extant metapopulations residing
in Miami-Dade and Sumter Counties are considered T. p. ssp. floridanum;
however, until recently, genetics sampling had not been conducted
providing conclusive evidence that these metapopulations are in fact
the same taxon. 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 well known (Woodmansee 2013, pers.
comm.); the specific life history of Trichomanes punctatum ssp.
floridanum, including information on other members of the genus, is
also lacking. Like all ferns, this taxon has two life-history stages, a
gametophyte stage and a sporophyte stage. However, only the sporophyte
form is recognizable in the wild, as spores of this plant are invisible
to the naked eye (Possley 2013a, pers. comm.; van der Heiden 2013b,
pers. comm.).
All reported populations of Trichomanes punctatum ssp. floridanum
have been in the sporophyte stage. The initial stage, after a spore
germinates, is 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 typical form
most ferns are observed in. The sporophytes produce spores, which in
turn can germinate to produce new gametophytes (Nelson 2000, pp. 17-
19). Reproduction may also occur in two other ways. Plants may
reproduce by division, when rhizomes (horizontal, underground plant
stems capable of producing the shoot and root systems of a new plant)
break, forming clones of the parent plant, or they may also reproduce
with the production of gemmae (cells that detach from the parent and
develop into a new individual) and propagules (a plant part that
becomes detached from the rest of the plant and grows into a new plant)
produced by gametophytes, which can grow into new gametophytes of the
same genotype (the genetic makeup of a cell or individual) (Dassler and
Farrar 2001, p. 354; Hill 2003, p. 12).
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 2013e, 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.
Recent field studies in Sumter County on extant Trichomanes
punctatum ssp. floridanum populations found average relative humidity
to be around 95 percent, while ambient temperatures were recorded to
stay around 23 degrees Celsius ([deg]C) (73 degrees Fahrenheit
([deg]F)). However, during cooler periods (19-22
[[Page 61139]]
[deg]C; 66-70[emsp14][deg]F) when humidity levels dropped slightly (to
around 92 percent humidity), observed plant health declined,
demonstrating the fragile nature of this taxon and its dependence on
high humid conditions (van der Heiden and Johnson 2014, p. 9). 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.
Organizations such as the Institute for Regional Conservation (IRC)
and Fairchild's Center for Tropical Plant Conservation (Fairchild) are
working together to understand the biology, life history, and
reproduction 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 has grown 14 separate clusters from plants
obtained in local hammocks (temperate hardwood forests) and 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 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
underway 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
(Holst 2014, pers. comm.).
Habitat
In southeastern North America, Trichomanes spp. are considered rare
because of their delicate nature and requirements for deeply sheltered
habitats with almost continuous high moisture and humidity (Farrar
1993b, 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 U.S. in the State of Florida. In
Florida, T. p. ssp. floridanum is only known to occur in Miami-Dade and
Sumter Counties.
Both extant metapopulations live in dense canopy habitats, with
shady conditions that may be obligatory due to the poikilohydric (i.e.,
possess 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 epiphytic (a plant that grows non-parasitically upon another
plant) or epipetric (growing on rocks), typically growing in rocky
outcrops of rockland hammocks, in oolitic (composed of minute rounded
concretions resembling fish eggs) limestone solution holes, 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 2013f, pers. comm.; van der Heiden 2014b, pers. comm.). These
rockland habitats are outcrops primarily comprised of marine limestone
representing the distinct geological formation of the Miami Rock Ridge,
a feature which 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 hammock
(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 consist of bare rock walls that 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 appearance of 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
[[Page 61140]]
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). Plants live in a
mesic hammock on limestone boulders 0.1-1.5 m (0.3-4.9 ft) tall (see
``Current Range'' section, 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, or 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). Historically, mesic
hammocks were thought to be restricted to naturally fire-protected
areas such as islands and peninsulas of lakes.
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 64 percent (van der
Heiden and Johnson 2013, pp. 8, 20). 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 2013, p. 7).
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). It has been suggested the northern aspect of limestone boulders
are 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 comprised 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, pp. 7, 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). Recent field surveys recorded 18 canopy species in Rocky
Hammock and 12 in Tree Frog Hammock (van der Heiden and Johnson 2014,
p. 19), both located in Sumter County. 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.
Habitat differences between Miami-Dade and Sumter Counties have
enabled this subspecies to adapt to very different conditions at each
location. In Miami-Dade, where Trichomanes punctatum ssp. floridanum
currently is found, the mean maximum temperature from the last 10 years
(2004-2013) was 29.0 [deg]C (84.3[deg]F), and the mean minimum
temperature for the same time period was 21.4 [deg]C (70.5[deg]F)
(https://www1.ncdc.noaa.gov). In contrast, yearly mean temperatures were
lower
[[Page 61141]]
for Sumter County with 23.4 [deg]C (74.2[deg]F) recorded as the maximum
temperature for the last 10 years (2004-2013), and 11.8 [deg]C
(53.2[deg]F) as the minimum temperature for the same time period
(National Oceanic and Atmospheric Administration 2014, https://www1.ncdc.noaa.gov). Although it is believed this subspecies needs high
temperatures and humidity, along with dense canopy, the exact
thresholds for these variables have yet to be determined.
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, 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 (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).
After the initial finding of 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.). Additional collections were obtained in
1903, in Castellow Hammock by A.A. Eaton with more recent observations
by G. Gann and K. Bradley in the late 1990s (Bradley and Gann 1999),
and J. Possley and others (Gann et al. 2002, pp. 552-554; Possley et
al. 2013, pp. 43-45). T. p. ssp. floridanum was collected in Silver
Palm Hammock in 1903, by A.A. Eaton and later reported again in 1980;
however, this 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 destroyed, and what remains is currently
protected as a Miami-Dade Conservation Area. 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., and subsequently reported as extirpated by
Gann et al. (2002, pp. 552-554), until it was rediscovered in this
hammock in 2011 by 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 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). Fuchs Hammock was also vouchered in
1993, following Hurricane Andrew (1992) by A. Cressler (Cressler 12
February 1993, handwritten notes,), and 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,
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 2013j, 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 existing 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.
[[Page 61142]]
Table 1--Summary of Historical Reports, Population Locations, and Current Population and Hammock Status of Trichomanes Punctatum ssp. Floridanum in
Miami-Dade County, Where Known
[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, j-k, 2014a-c; Possley 2013, 2014 pers. comm.; Gann 2013, pers. comm.; van
der Heiden 2013e, pers. comm.; Gann 2014a-f, pers. comm.; Gann et al. 2014, https://regionalconservation.org/ircs/database/plants/PlantPage.asp?TXCODE=Tricpuncflor]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Year(s)
of Number of Current population Current hammock
No. Population location initial Observer specimens status status
report(s) collected
--------------------------------------------------------------------------------------------------------------------------------------------------------
1................................. Deering-Snapper Creek 1901 J.K. Small, G.V. Nash 3 Extirpated........... Protected Area,
Hammock (in R. Hardy 1915 J.K. Small, C.A. 1 Partially
Matheson Preserve). Mosier. Destroyed.
2................................. Castellow Hammock...... 1903 J.K. Small, J.J. 2 Extant............... Protected Area.
1903 Carter. 4
A.A. Eaton...........
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 1917 Carter. None
Key. W.E. Stafford........
6................................. Hattie Bauer Hammock 1915 J.K. Small, C.A. 2 Extant............... Protected Area.
(Orchid Jungle). 1915 Mosier. 3
J.K. Small...........
1915 J.K. Small, C.A. 5
Mosier, G.K. Small.
1916 J.K. Small........... 1
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). 1954 Mosier. 1
L.J. Brass...........
1959 T. Darling Jr........ 1
1969 A.F. Clewell, F.C. 1
Craighead.
10................................ Addison Hammock 1916 J.K. Small........... None Unknown \1\.......... Protected Area.
(Deering Estate at
Cutler).
11................................ Matheson Hammock Park.. 1940 G. Peterson.......... 2 Unknown \2\.......... Protected Area.
12................................ Meissner Hammock....... 1983 G.N. Avery........... None Extant............... Protected Area.
13................................ Cox Hammock (Monkey 1989 A. Cressler.......... None Unknown \3\.......... Privately Owned,
Jungle). Partially
Destroyed.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ Initial report is questionable.
\2\ Precise location of sample and associated report is questionable.
\3\ It is not known whether the species still occurs here.
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
[[Page 61143]]
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 S.W. 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, which is now
extirpated.
Table 2--Summary of Historical Reports, Population Locations, and Current Population and Hammock Status of Trichomanes punctatum ssp. floridanum in
Sumter County, Where Known
[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. 2014, https://regionalconservation.org/ircs/database/plants/PlantPage.asp?TXCODE=Tricpuncflor]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Year of Number of
No. Population location initial Observer specimens Current population Current hammock
report collected status status
--------------------------------------------------------------------------------------------------------------------------------------------------------
1................................. 11.26 km (7 mi) East of 1936 R.P. St. John........ 1 Presumed Extirpated.. Privately Owned,
Floral City \1\. Presumed Destroyed.
2................................. Floral City Area \1\... 1939 J.B. McFarlin........ 1 Unknown \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 Unknown \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 of 1983 S.W. Leonard......... 1 Extirpated........... Privately Owned,
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).
Miami-Dade County
The four populations that constitute the Miami-Dade County
metapopulation are located in urban preserves managed by the County's
Environmentally Endangered Lands (EEL) Program (see Factor A,
Conservation Efforts to Reduce Habitat Destruction, Modification, or
Curtailment of Its Range, below). These EEL properties 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 subpopulations in Fuchs Hammock
include a new population 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. During 2011, another population was re-discovered at Hattie
Bauer Hammock (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.
In general, Trichomanes punctatum ssp. floridanum occurs in small areas
within each hammock.
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 2013f, 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 2013g, pers. comm.). A plant 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; however, plants 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 (in ENP) for other rare plants were also 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
[[Page 61144]]
approximately 1,478 ha (3,652 ac) in Sumter County. However, not all of
these areas have been systematically surveyed. Although surveys
conducted of a boulder field within Withlacoochee State Forest's Jumper
Creek Tract (called the Indian Field Ledges) in August 2007 and April
2013 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.).
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 (WSF)
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
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.
Table 3--Summary of Known Extant Occurrences of Trichomanes punctatum ssp. floridanum. (Possley 2013, p. 1-2;
Dozier 2014, pers. comm.; van der Heiden and Johnson 2014, pp. 1-3).
----------------------------------------------------------------------------------------------------------------
Number of
Metapopulation location (County) Population location Land ownership subpopulations Status
----------------------------------------------------------------------------------------------------------------
Miami-Dade....................... Meissner Hammock.... State.............. 2 Extant.
Miami-Dade....................... Fuchs............... County............. 4 Extant.
Miami-Dade....................... Castellow........... County............. 3 Extant.
Miami-Dade....................... Hattie Bauer........ 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.
----------------------------------------------------------------------------------------------------------------
Population Estimates and Status
Trichomanes punctatum ssp. floridanum grows in dense mats and is
rhizomatous (a horizontal stem that often sends out roots and shoots
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). 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 Hole (no tag)...... 0.078............. 2-10
Hammock.
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 m\2\........ ................
Sumter.......................... Rocky Hammock...... N/A................ 4.355............. 44
Sumter.......................... Tree Frog Hammock.. N/A................ 0.132............. 4
[[Page 61145]]
Sumter County Total......... ................... ................... 4.487 m\2\........ ................
-------------------------------------------------------------------------------
Total Area Covered.......... ................... ................... 14.407 m\2\....... ................
----------------------------------------------------------------------------------------------------------------
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 2013h, 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 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.
Each of these factors as applied to Trichomanes punctatum ssp.
floridanum is discussed below.
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 the species responds negatively, the
factor may be a threat, and we then attempt to determine if that factor
rises to the level of 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 found have 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, https://www.fnai.org/PDF/NC/Rockland_Hammock_Final_2010.pdf). 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,
[[Page 61146]]
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 destroyed Ross Hammock (Phillips 1940, p. 167).
Rockland hammock habitat is now limited to public conservation
lands 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).
Due to the possibility that additional populations of Trichomanes
punctatum ssp. floridanum may be found on private property and could be
destroyed, and the fact that there are no guarantees that the limited
rockland hammock habitat will remain as public conservation land in
perpetuity, 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 and in existing conservation
areas.
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.). Although undeveloped land is more abundant in
Sumter County than in Miami-Dade County, the fact that no virgin land
remains within Sumter County may reduce the likelihood of new
populations being discovered (Farnsworth 2013, 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 and within
existing conservation areas, 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 extirpation and 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 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 for 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
[[Page 61147]]
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, it is possible in the
future. Minimum flows and levels (MFLs), which are water withdrawal
standards to limit water use set the by regional Water Management
Districts (WMDs), 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 table use, it is believed 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
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.
As a hygrophilous (living or growing in damp places) subspecies
thought to be restricted to a consistent humid microhabitat
(Kr[ouml]mer and Kessler 2006, p. 57), high humidity is a critical
factor to its survival; any habitat modification or destruction that
changes ambient humidity levels is believed to be 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 2013f, pers. comm.). Van der
Heiden and Johnson (2013, 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 is also 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 avoid desiccation from
excessive light exposure (van der Heiden 2013c, pers. comm.; Possley
2013f, pers. comm.; Adimey 2013a-b, field notes). Currently, in both
metapopulations, dense canopy cover is a necessity; however, the lower
limits of canopy density needed to ensure survival are 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
2013h, 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, canopy loss is believed to be a limiting factor for the
future persistence of the subspecies and is therefore considered a
threat to T. p. spp. 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, fragmented 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, thorough knowledge of the
impacts and subsequent consequences from habitat fragmentation is
unknown for both metapopulations of Trichomanes punctatum ssp.
floridanum because information and understanding of dispersal
mechanisms for this subspecies is currently lacking. The best available
data regarding the impacts of habitat fragmentation on other plant
species suggests 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 in which both metapopulations
occur. All known 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
(https://www.miamidade.gov/environment/endangered-lands.asp).
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 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
[[Page 61148]]
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 owned by the Miami-Dade County
Parks, Recreation and Open Spaces 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). A precursor to the EEL Program is the EEL
Covenant Program, which regulates private lands for conservation
through easements.
EEL Covenant Program
In 1979, Miami-Dade County enacted the EEL Covenant Program, which
reduces taxes for private landowners of natural forest communities
(NFC) such as pine rocklands and rockland hammocks. Under the EEL
Covenant Program, landowners agree not to develop their property and
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 regulates 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
hammocks 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).
These County- and State-owned land areas are critical to protecting
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 underway for many years. In Miami-Dade County, conservation lands
are and have been monitored by Fairchild and IRC, in coordination with
the EEL Program, to assess habitat status and determine any changes
that may pose a threat to or alter the abundance of T. p. ssp.
floridanum (Possley 2013m, 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.
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 without further explanation (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). This is not surprising since 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. floridanum was found in
an additional nine hammocks in Miami-Dade County. These populations
have been extirpated, and the historical range of the southern
metapopulation has been reduced by nearly 80 percent. Although much of
the habitat has been destroyed and 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. floridanum currently exists are still vulnerable
to activities in the surrounding areas including agricultural clearing
and hydrologic alterations.
The Sumter County metapopulation of Trichomanes puctatum ssp.
floridanum is composed of two known 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 continues to be a threat to T. p. floridanum
populations and habitat. Although historical habitat modification and
destruction in Sumter County has not been as extensive as in South
Florida, this is a future potential threat due to the large areas of
undeveloped lands within Sumter County.
The destruction and modification of habitats 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 puctatum ssp. floridanum's
survival; therefore, any habitat modification or destruction that
changes ambient humidity levels or canopy cover poses a threat to this
subspecies. Thorough knowledge of the impacts of habitat fragmentation
is unknown for both metapopulations of T. p. ssp. floridanum because
information on dispersal mechanisms of this
[[Page 61149]]
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. Water withdrawals may
still be of some concern; however, the impact of this factor is not
currently known, and therefore, we have determined it to be a stressor,
but it is not rising to the level of a threat at this time.
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 puctatum 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 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 to determine whether they effectively reduce or remove
threats to Trichomanes punctatum ssp. floridanum.
Federal
The only known extant populations of Trichomanes punctatum ssp.
floridanum occur on State- or County-owned properties and development
of these areas will likely require no Federal permit or other
authorization. Therefore, projects that affect T. p. ssp. floridanum on
State- and County-owned lands do not have a Federal oversight, such as
complying with the National Environmental Policy Act (NEPA) (42 U.S.C.
4321 et seq.), unless the project has a Federal nexus (Federal funding,
permits, or other authorizations). Therefore, T. p. ssp. floridanum has
no direct Federal regulatory protection in its known occupied habitats.
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, https://fnai.org/PDF/Element_tracking_summary_current.pdf). The IRC considers its status as
``critically imperiled'' (Gann et al. 2002, pp. 552-554).
The Florida Department of Agriculture and Consumer Services (FDACS)
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: https://www.flrules.org/gateway/RuleNo.asp?title=PRESERVATION%20OF%20NATIVE%20FLORA%20OF%20FLORIDA&ID=5B-40.0055). 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 protection for State-
listed plants on private lands. Florida Statutes 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. Subsections
(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, https://www.leg.state.fl.us/Statutes/index.cfm?Mode=View%20Statutes&Submenu=1&Tab=statutes). 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 there is no imminent threat to Withlacoochee State Forest
being modified (e.g., logged), altered (e.g., installation of
pipelines), or sold for
[[Page 61150]]
development, the State may be allowed to proceed with such actions only
after they have been reviewed and approved at public meetings by the
Acquisition and Restoration Council (ARC) and, depending upon the
issue, by the Board of Trustees of the Internal Improvement Trust Fund
of the State of Florida.
Although the MFLs established by the South Florida Water Management
District (SFWMD) in southeast Florida (a separate entity than the
Southwest Florida Water Management District (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
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 oftentimes 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, RER pursues unpermitted work through
appropriate enforcement action and seeks restoration 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 on a parcel
in limited circumstances for parcels less than 2.02 ha (5 ac) in size
and only requires coordination with the landowner 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 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 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. Any undocumented occurrences of T. p.
ssp. floridanum and suitable habitat on private lands are at risk. 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, there is still a significant
portion of the hammock that 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. The landowner could apply for a
permit and destroy undocumented populations of T. p. ssp. floridanum
and the subspecies' habitat on this site. Because the site is private
and not managed as
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a preserve (i.e., it is not controlled for nonnative, invasive plant
species), degradation of potential habitat for T. p. ssp. floridanum is
likely. Furthermore, a change in ownership, accompanied by subsequent
modifications in land-use, may cause extirpation of any undocumented T.
p. ssp. floridanum populations or negatively impact suitable habitat.
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.).
Because a comprehensive survey in Sumter County has not yet been
conducted, there is a chance of finding new populations of Trichomanes
punctatum ssp. floridanum in the area. Any undocumented occurrences and
suitable habitat that could be important for reintroduction or
recolonization of this subspecies in Sumter County, especially on
private lands, are potentially at risk due to development. Under
section 13-644(a)(1) of the 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,
County code prevents unmitigated destruction of endangered, threatened,
or rare species only when associated with ``major developments.''
However, these sections do not prevent land destruction or development
on private land where any undocumented populations of T. p. ssp.
floridanum or suitable habitat for future reintroduction are
vulnerable. 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 found only on
State and County lands; however, there is no regulatory mechanism in
place that provides 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-wetlands) 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 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 are 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, promoting overshading and forming dense strata (layers)
in hammocks, which alter the habitat and its surrounding conditions
(Possley 2013f, pers. comm.). It has also been suggested that the
insular nature of south Florida, as well as the hammocks themselves,
predispose this habitat to 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, as management in these areas
generally does not protect native species and ecological processes, as
intended. Problematic nonnative invasive plants in Miami-Dade County
associated with Trichomanes punctatum ssp. floridanum include Schinus
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terebinthifolius (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 2013h-i, 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 2014, 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 and
removing the nonnative species exposes the fern. In the case of
Castellow Hammock, the majority of the shade near two of the large
solution holes containing Trichomanes punctatum ssp. floridanum is
provided by giant Schinus terebinthifolius 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. terebinthifolius canopy has already occurred. In this
case, the subpopulation of T. p. ssp. floridanum below where the S.
terebinthifolius tree was turned brown; however, T. p. ssp. floridanum
could eventually revitalize if sufficient canopy is re-established to
limit sunlight exposure (Possley 2013e, pers. comm.). Additionally,
nonnative plant control may also become a threat when T. p. ssp.
floridanum are inadvertently sprayed while conducting local nonnative
removal efforts (Possley 2013e, 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.
Undiscovered populations of Trichomanes punctatum ssp. floridanum on
private lands could certainly be at risk. 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 laying against or rubbing their bodies
against large rocks, removing existing vegetation in the process.
Recently, van der Heiden and Johnson (2013, 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
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 Liguus (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 be 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 Intergovernmental Panel on Climate
Change (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, pp. 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 (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
[[Page 61153]]
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 groundwater 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 in 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 which extends
from the top of the ground surface to the water table); increase
salinity in the bottom portion of the freshwater lens, thereby
increasing brackishness of plant-available water; and influence tree
species composition of coastal 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 such as Trichomanes punctatum ssp. floridanum.
Shifts in freshwater flows, annual precipitation, and variability in
SLR can impact salinity regimes. Although it is unknown if salinity
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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, this 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, 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
exogenous stresses can improve resiliency 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
resilience, population growth, and potential for natural dispersal, and
controlling for nonnative species. Efforts to actively manage for
resilience are currently limited for both metapopulations of T. p. ssp.
floridanum due to logistic feasibility, 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 large 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 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 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
[[Page 61155]]
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
susceptible 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 and environmental 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 one 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 hurricane and
tropical storm frequencies in the Atlantic are expected to decrease
between 10-30 percent by 2100 (Knutson et al. 2008, pp. 1-21). For
those models that predict fewer hurricanes, predictions of 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 hammocks 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
believed to be the threat with greatest impact to existing
metapopulations of Trichomanes punctatum ssp. floridanum (Adimey 2013b,
field notes; Possley 2013p, pers. comm.). For example, impacts from
Hurricane Andrew in 1992 were thought to be responsible for the
temporary loss of this subspecies from Hattie Bauer Hammock, where it
had been observed for many years. Following this hurricane, the canopy
was destroyed, allowing increased exposure to sunlight for several
years. T. p. ssp. floridanum was not seen again in Hattie Bauer Hammock
until 2011 (Possley 2013p, 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 original 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 small population size, 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 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. Multi-year droughts may negatively impact populations. While
droughts are natural events, they are a threat because there are so few
populations of this subspecies. Specific range requirements regarding
humidity, temperature, and precipitation 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
[[Page 61156]]
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, its genetic variability and overall
resilience is likely low. These factors, combined with additional
stress from habitat modifications (e.g., hydrological changes) may
increase the inherent risk of 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 as
addressed above are a threat to the persistence of this subspecies in
the future (Adimey 2013b, field notes; Possley 2013p, 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 influenced the
occurrence of fire; 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 (1916, https://www.floridamemory.com/items/show/49132;
1917, https://www.floridamemory.com/items/show/49465). 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.
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 (Werner 2013d,
pers. comm; Possley 2013l, pers. comm.).
Snyder (et al. 1990, p. 238) points out that the high organic
content of hammock soils in south Florida can enable it to burn;
however, soil fires typically only burn in hammocks in times of drought
or when they 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, the natural fire-resistant
features of these two habitats, and, in Sumter County, hydric hammock
surrounding Trichomanes punctatum ssp. floridanum populations. However,
under future projected climate change scenarios, we expect drought
conditions to exacerbate the effects on T. p. ssp. floridanum to a
level at which fire becomes a threat in the future.
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 2013h, 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 does not
appear to be occurring at this time, and we have determined it does not
pose a threat to T. p. ssp. floridanum.
Small Population Size and Isolation
Low population resilience is a serious concern for species that are
restricted to geographically limited areas, as they are inherently more
vulnerable to extinction than widespread species due to an increased
risk of genetic bottlenecks, random demographic fluctuations, climate
change, and localized catastrophes such as hurricanes and disease
outbreaks (Mangel and Tier 1994, p. 607; Pimm et al. 1988, p. 757).
These problems are further magnified when populations are few,
populations are restricted to very small geographic areas, and numbers
of individuals are limited, as in the case of Trichomanes punctatum
ssp. floridanum. 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 is also a stressor that contributes to
the low population resilience for this subspecies (see ``Habitat
Fragmentation'' under Factor A).
Limited genetic variability will also impact population resilience.
The ability of populations 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, with few
plants, the genetic variability is considered low, and the subspecies
is inherently at risk due to stochastic events and changes in
environmental
[[Page 61157]]
conditions (Matthies et al. 2004, pp. 481-488).
In summary, population resilience 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 low population resilience to Trichomanes
punctatum ssp. floridanum that could arise due to small population
size, 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 extinction from one location
would occur.
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 manager for further attention (Possley 2013p, pers.
comm.). IRC also conducts research and monitoring in various 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. This is especially alarming since droughts, tropical
storms, and hurricanes are common occurrences in Florida. 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 cause 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.
Proposed Determination
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 (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.
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 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
[[Page 61158]]
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, are isolated, and have limited to no potential 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 in light of the fact these
events cannot be controlled and mitigation measures have yet to be
addressed. Individually and collectively, all 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 propose to
list 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 ongoing, and are expected to
continue into the future.
Under the Act and our implementing regulations, a species may
warrant listing if it is endangered or threatened throughout all or a
significant portion of its range. The threats to the survival of
Trichomanes punctatum ssp. floridanum occur throughout the subspecies'
range and are not restricted to any particular significant portion of
that range. Accordingly, our assessment and proposed determination
applies to the subspecies throughout its entire range.
Significant Portion of the 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 Service's SPR Policy (79 FR 37578, July 1, 2014).
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened under the Act include recognition, recovery actions,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing results in public awareness and
conservation by Federal, State, 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 to
threatened) 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. If we
list Trichomanes punctatum ssp. floridanum, when completed, the draft
and final recovery plans would 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.
If this subspecies is listed, funding for recovery actions would 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 would 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
[[Page 61159]]
to aid species recovery can be found at: https://www.fws.gov/grants.
Although Trichomanes punctatum ssp. floridanum is only proposed for
listing under the Act at this time, please let us know if you are
interested in participating in conservation efforts for this species.
Additionally, we invite you to submit any new information on this
species whenever it becomes available and any information you may have
for conservation planning purposes (see FOR FURTHER INFORMATION
CONTACT).
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is proposed or listed as 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)(4) of the Act requires Federal agencies to
confer with the Service on any action that is likely to jeopardize the
continued existence of a species proposed for listing or result in
destruction or adverse modification of proposed critical habitat. If a
species is listed subsequently, section 7(a)(2) of the Act requires
Federal agencies to ensure that activities they authorize, fund, or
carry out are not likely to jeopardize the continued existence of the
species or destroy or adversely modify its critical habitat. If a
Federal action may affect a listed species or its critical habitat, the
responsible Federal agency must enter into consultation with the
Service.
Federal agency actions within the subspecies' 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 and any other landscape-altering activities.
With respect to endangered plants, prohibitions outlined at 50 CFR
17.61 make it illegal for any person subject to the jurisdiction of the
United States to import or export, transport in interstate or foreign
commerce in the course of a commercial activity, sell or offer for sale
in interstate or foreign commerce, or 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 outlined 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 proposed
listing on proposed and ongoing activities within the range of the
species proposed for listing. If we list Trichomanes punctatum ssp.
floridanum, 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.
At this time, we are unable to identify specific activities that
would not be considered to result in a violation of section 9 of the
Act because Trichomanes punctatum ssp. floridanum occurs in a variety
of habitat conditions across its range and it is likely that site-
specific conservation measures may be needed for activities that may
directly or indirectly affect the subspecies.
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.''
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.
As discussed in the Factor B analysis (see above), there is
currently no imminent threat of take attributed to collection or
vandalism for this species, and identification and mapping of critical
habitat is not expected to initiate any such threat. Therefore, in the
[[Page 61160]]
absence of finding that the designation of critical habitat would
increase threats to a species, if there are any benefits to a critical
habitat designation, a finding that designation is prudent is
warranted. Here, the potential benefits of designation include: (1)
Triggering consultation under section 7 of the Act, in new areas for
actions in which there may be a Federal nexus where it would not
otherwise occur because, for example, it is unoccupied; (2) focusing
conservation activities on the most essential features and areas; (3)
providing educational benefits to State or county governments or
private entities; and (4) preventing people from causing inadvertent
harm to the species.
Because we have 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 determine that designation of
critical habitat is prudent for Trichomanes punctatum ssp. floridanum.
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 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.
Our regulations at 50 CFR 424.19 require the Service to ``make
available for public comment the draft economic analysis of the
designation'' at the time the proposed critical habitat rule is
published in the Federal Register. At this point, a careful assessment
of the economic impacts that may occur due to a critical habitat
designation is still ongoing, and we are still in the process of
acquiring the information needed to perform this assessment.
Accordingly, we find designation of critical habitat for Trichomanes
punctatum ssp. floridanum to be not determinable at this time.
Required Determinations
Clarity of the Rule
We are required by Executive Orders 12866 and 12988 and by the
Presidential Memorandum of June 1, 1998, to write all rules in plain
language. This means that each rule we publish must:
(1) Be logically organized;
(2) Use the active voice to address readers directly;
(3) Use clear language rather than jargon;
(4) Be divided into short sections and sentences; and
(5) Use lists and tables wherever possible.
If you feel that we have not met these requirements, send us
comments by one of the methods listed in the ADDRESSES section. To
better help us revise the rule, your comments should be as specific as
possible. For example, you should tell us the numbers of the sections
or paragraphs that are unclearly written, which sections or sentences
are too long, the sections where you feel lists or tables would be
useful, etc.
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 need not be prepared in connection with
listing a species as an endangered or threatened species under the 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 proposed 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.
Proposed Regulation Promulgation
Accordingly, we propose to amend part 17, subchapter B of chapter
I, title 50 of the Code of Federal Regulations, as set forth below:
PART 17--[AMENDED]
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 16 U.S.C. 1531-1544; 16 U.S.C.
4201-4245, 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) * * *
[[Page 61161]]
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Species
-------------------------------------------------------- Historic range Family Status When listed Critical Special
Scientific name Common name habitat rules
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* * * * * * *
FERNS AND ALLIES
* * * * * * *
Trichomanes punctatum ssp. Florida bristle fern U.S.A. (FL)........ Hymenophyllaceae... E NA NA.
floridanum.
* * * * * * *
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* * * * *
Dated: September 26, 2014.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2014-23686 Filed 10-8-14; 8:45 am]
BILLING CODE 4310-55-P