Endangered and Threatened Wildlife and Plants; Removal of Chrysopsis floridana (Florida Golden Aster) From the Federal List of Endangered and Threatened Plants, 15763-15779 [2024-04278]
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[FR Doc. 2024–04587 Filed 3–4–24; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF DEFENSE
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Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R4–ES–2019–0071;
FF09E22000 FXES1113090FEDR 2223]
RIN 1018–BE00
Endangered and Threatened Wildlife
and Plants; Removal of Chrysopsis
floridana (Florida Golden Aster) From
the Federal List of Endangered and
Threatened Plants
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), are removing
the Florida golden aster (Chrysopsis
floridana), a short-lived perennial, from
the Federal List of Endangered and
Threatened Plants (List) due to recovery.
Our review indicates that the threats to
the species have been eliminated or
reduced to the point that the species has
recovered and no longer meets the
definition of an endangered or
threatened species under the
Endangered Species Act of 1973, as
amended (Act). Accordingly, the
prohibitions and conservation measures
provided by the Act will no longer
apply to this species.
DATES: This rule is effective April 4,
2024.
SUMMARY:
This final rule, supporting
documents used in preparing this rule,
the post-delisting monitoring plan, and
the comments we received on the June
24, 2021, proposed rule are available at
https://www.regulations.gov under
Docket No. FWS–R4–ES–2019–0071.
FOR FURTHER INFORMATION CONTACT:
Lourdes Mena, Division Manager,
Florida Classification and Recovery,
U.S. Fish and Wildlife Service, Florida
Ecological Services Field Office, 7915
Baymeadows Way, Jacksonville, FL
32256; telephone 904–731–3336.
Individuals in the United States who are
deaf, deafblind, hard of hearing, or have
a speech disability may dial 711 (TTY,
TDD, or TeleBraille) to access
telecommunications relay services.
Individuals outside the United States
should use the relay services offered
within their country to make
international calls to the point-of
contact in the United States.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
GENERAL SERVICES
ADMINISTRATION
[FR Doc. C1–2024–02798 Filed 3–4–24; 8:45 am]
DEPARTMENT OF THE INTERIOR
Executive Summary
Why we need to publish a rule. Under
the Act, a species warrants delisting if
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15763
it no longer meets the definition of an
endangered species (in danger of
extinction throughout all or a significant
portion of its range) or threatened
species (likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range). The Florida golden aster is
listed as an endangered species, and we
are delisting it. Delisting a species can
only be completed by issuing a rule
through the Administrative Procedure
Act rulemaking process (5 U.S.C. 551 et
seq.).
What this document does. This rule
removes the Florida golden aster from
the Federal List of Endangered and
Threatened Plants based on the species’
recovery.
The basis for our action. Under the
Act, we may determine that a species is
an endangered or threatened species
because of 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. The
determination to delist a species must
be based on an analysis of the same
factors.
Under the Act, we must review the
status of all listed species at least once
every 5 years. We must delist a species
if we determine, based on the best
available scientific and commercial
data, that the species is neither an
endangered species nor a threatened
species. Our regulations at 50 CFR
424.11(e) identify three reasons why we
might determine a species should be
delisted: (1) The species is extinct, (2)
the species does not meet the Act’s
definition of an endangered species or a
threatened species, or (3) the listed
entity does not meet the Act’s definition
of a species. Here, we have determined
that the Florida golden aster does not
meet the definition of an endangered
species or a threatened species;
therefore, we are delisting it.
Previous Federal Actions
Please refer to the proposed delisting
rule (86 FR 33177) for the Florida
golden aster published on June 24, 2021,
for a detailed description of previous
Federal actions concerning this species.
Peer Review
A species status assessment (SSA)
team prepared an SSA report for the
Florida golden aster. The SSA team was
composed of Service biologists, in
consultation with other species experts.
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The SSA report represents a
compilation of the best scientific and
commercial data available concerning
the status of the species, including the
impact of past, present, and future
factors (both negative and beneficial)
affecting the species.
In accordance with our joint policy on
peer review published in the Federal
Register on July 1, 1994 (59 FR 34270),
and our August 22, 2016, memorandum
updating and clarifying the role of peer
review in listing actions under the Act,
we solicited independent scientific
review of the information contained in
the Florida golden aster SSA report. As
discussed in the proposed rule, we sent
the SSA report to six independent peer
reviewers and received two responses.
The peer reviews can be found at
https://www.regulations.gov. In
preparing the proposed rule, we
incorporated the results of these
reviews, as appropriate, into the SSA
report, which was the foundation for the
proposed rule and this final rule. A
summary for the peer review comments
and our responses can be found in the
Summary of Comments and
Recommendations below.
Summary of Changes From the
Proposed Rule
In this final rule, we make no
substantive changes to our June 24,
2021, proposed rule. Minor,
nonsubstantive changes have been made
throughout this final rule.
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Summary of Comments and
Recommendations
In the proposed rule published on
June 24, 2021 (86 FR 33177), we
requested that all interested parties
submit written comments on our
proposal to delist the Florida golden
aster and the draft post-delisting
monitoring (PDM) plan by August 23,
2021. We also contacted appropriate
Federal and State agencies, scientific
experts and organizations, and other
interested parties and invited them to
comment on the proposal. A newspaper
notice inviting public comments was
published on June 30, 2021, in the
Tampa Bay Times. We did not receive
any requests for a public hearing. All
substantive information provided
during the comment period is addressed
below.
Peer Reviewer Comments
As discussed in Peer Review above,
we received comments from two peer
reviewers on the draft SSA report. The
SSA report was also submitted to our
Federal, State, and Tribal partners for
scientific review. We received review
from two partners. We reviewed all
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comments we received from the peer
and partner reviewers for substantive
issues and new information regarding
the contents of the SSA report. The
reviewers did not raise any substantive
issues and provided only editorial
comments that we incorporated into the
final SSA report, which was the
foundation for the proposed rule and
this final rule.
Public Comments
We reviewed all public comments for
substantive issues and new information
regarding the species. Substantive
comments we received during the
comment period are addressed below.
(1) Comment: Several commenters
stated the species should not be delisted
because populations are performing
poorly. Multiple commenters pointed to
the report titled, ‘‘Demographic Data
Collection to Assess the Endangerment
of Chrysopsis floridana 2020’’ (Peterson
et al. 2020, entire) as supporting their
position that the species should not be
delisted.
Our response: The report titled,
‘‘Demographic Data Collection to Assess
the Endangerment of Chrysopsis
floridana 2020’’ (Peterson et al. 2020,
entire) was funded by the Service to
analyze a subset of known populations
and did not look at all known
populations. The intent of the effort was
to collect data to provide additional
information to supplement the 2018
Florida golden aster SSA report. The
results of Peterson et al. (2020, entire)
reinforce our determination that the
Florida golden aster no longer meets the
Act’s definition of an endangered
species or a threatened species.
The 18 sites for the report were
chosen specifically based on aster
population size and habitat
development risk, which results in
increased future management
constraints. Eleven of the selected
populations were classified as low risk,
and the remaining seven were classified
as high risk, based on modeling
projections in the SSA report (Service
2018, p. 35). Of the 18 populations
analyzed for the report, all populations
were analyzed for demographic data,
and 8 of those also had stage class (i.e.,
seedlings, vegetative plants,
reproductive plants) data collected. Data
were collected over a 3-year period, and
annual survival and annual seedling
survival were calculated each year. This
approach was intended to provide an
analysis of the variation in populations
across the species’ range, looking at
population resiliency and habitat
management effectiveness. The analysis
was a comparison of the populations’
metrics between the populations
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studied but is not comparable to the
overall current condition of the species.
Stage structure was used as an indirect
measure of population health because
fecundity data (seed production) were
not collected, and full demographic
models could not be assembled for the
species.
Annual survival was variable among
populations and across years. Stage
structure (‘‘small vegetative’’ plants,
‘‘large vegetative’’ plants, and
‘‘reproductive’’ plants) also varied over
the 3-year period, with demographically
healthy populations having more
seedlings and the least healthy
populations having more flowering
plants. This variation would be
expected based on the annual variations
in climate conditions over time as well
as the phenology of the species.
Demographic results indicated moderate
annual survival rates for 2017–2018
(75.6 percent) and 2018–2019 (71.8
percent). The annual survival rate for
the 2017–2018 populations ranged from
55–91 percent with similar rates of 42–
89 percent in 2018–2019. The annual
seedling survival (62.0 percent and 64.6
percent, respectively) was slightly
lower. The report concluded that at least
6 populations might be considered
healthy and self-sustaining, and it may
be determined that the other 12
populations (all on protected lands) will
fare better in future years given
increased management efforts (ideally
fire), especially within wild
populations.
Variation in survival rates could be
attributed to the time since the last fire,
habitat management application, and/or
age of the mature plant during the study
period. Florida golden aster is a shortlived perennial (3–5 years) that flowers
multiple years once reproductive. Not
knowing the age of the plants being
analyzed over the short timeframe in the
randomly selected plots could have
biased the results, as some of the plants
may have been already at the end of
their lifespan or not reproductive yet. In
addition, consideration of early versus
late lifespan productivity or species
cycles (phenology), which are currently
unknown, may be important factors
influencing the analyzed data. The
survival rate for this species is described
as moderate; the annual survival rates
for this aster are adequate for the species
and the habitat it occupies (Peterson et
al. 2020, entire). Although survival rates
varied among introduced and wild
populations and varied based on the
habitat management status of the
population, populations consistently
showed seedling recruitment, which is
an indication of recruitment in all
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populations regardless of health
conditions.
Based on the most current survey
across the species’ range (2006–2018),
30 known extant populations, natural
and introduced, occur in five counties.
Of these, 25 populations occur on 22
protected and managed conservation
lands. The post-delisting monitoring
plan will utilize baseline data for the
populations studied in the report to
further assess long-term trends.
(2) Comment: Some commenters
stated the species should not be delisted
because recovery criteria for delisting
have not been achieved.
Our response: Recovery plans provide
a roadmap for us and our partners on
methods of enhancing conservation and
minimizing threats to listed species, as
well as measureable criteria against
which to evaluate progress towards
recovery and assess the species’ likely
future condition. However, they are not
regulatory documents and do not
substitute for the determinations and
promulgation of regulations under
section 4(a)(1) of the Act. A decision to
delist a species is ultimately based on
an analysis of the best scientific and
commercial data available and
consideration of the standards listed in
50 CFR 424.11(e) to determine whether
a species is no longer an endangered
species or a threatened species,
regardless of whether that information
differs from the recovery plan.
According to the recovery plan there are
many paths for this species to be
recovered without all the criteria being
fully met. The recovery plan states that
one or more criteria may be exceeded
while other criteria may not yet be
accomplished. In this instance, we have
determined that the threats to Florida
golden aster are minimized sufficiently
and that the species no longer meets the
Act’s definition of an endangered
species or a threatened species.
(3) Comment: One commenter
indicated delisting was premature
because there was no data-driven
management plan for the species. The
commenter further stated that while
short-term monitoring has suggested a
role for fire in maintaining populations,
critical data are lacking pertaining to the
best management practices to maintain
Florida golden aster habitat, specifically
disturbance dynamics and the optimal
fire frequency for managing
populations.
Our response: In our June 24, 2021,
proposed rule (86 FR 33177), we
announced the availability of a draft
PDM plan for the Florida golden aster,
and we requested comments on the draft
PDM plan. We also solicited comments
on the draft PDM plan from agencies
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that manage Florida golden aster on
their conservation lands, as well as State
and county partners that have been
engaged in the species’ conservation.
We received comments from both the
Florida Forest Service and Hillsborough
County’s Environmental Lands
Acquisition and Protection Program,
and their comments were incorporated
into the final PDM plan. See Postdelisting Monitoring, below, for more
information.
The decision to revise the status of a
species, or to delist a species, is
ultimately based on an analysis of the
best scientific and commercial data
available to determine whether a species
is no longer an endangered species or a
threatened species. Complete
understanding of specific data
pertaining to best management practices
for Florida golden aster such as
disturbance dynamics or the fire return
intervals for optimal survival and
health, is not a requirement of the Act.
Nevertheless, the general response of
Florida golden aster to disturbance
regimes is sufficiently understood to
inform management. The delisting of
Florida golden aster should not
discourage continued research on the
species and its habitat needs. Indeed,
the PDM plan includes
recommendations for this type of
research.
(4) Comment: One commenter noted
that growing development surrounding
Florida golden aster populations will
further complicate fire management,
which is important for maintaining
suitable habitat. It will become
increasingly difficult for many areas
where Florida golden aster is present to
be managed with fire, and there is little
evidence that mechanical disturbance
could serve as an effective surrogate for
fire.
Our response: The development
pressures on native landscapes
throughout peninsular Florida are
challenging and will continue to persist
indefinitely. Habitat management on
conservation lands in the wildlandurban interface can experience various
constraints. However, not all
conservation lands with Florida golden
aster populations are subject to these
constraints, and development often does
not preclude fire management; for
example, the national wildlife refuges in
Florida frequently conduct prescribed
fires despite close proximity to
developed areas. Additionally, various
treatments and techniques to prepare
fuel loads prior to prescribed fire
application can also overcome many of
these constraints, along with managing
the area without the use of fire. New
and innovative methods are constantly
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being developed and employed to
accomplish the desired habitat
conditions. Best management practices
and sound management planning
alleviates many of the obstacles land
managers encounter when pursing
optimal conditions in support of the
targeted species.
While the commenter stated that
mechanical disturbance is not as
effective as fire in maintaining habitat
for the Florida golden aster, mechanical
treatments can be effective, if deployed
correctly. We note in the SSA report
that in the absence of fire, habitat
openness can be maintained with
mowing, hand removal of trees and
shrubs near plants, or other mechanical
treatments. Populations have persisted
along periodically mowed rights-of-way
(e.g., underneath powerlines, along
roads and railroads) for decades without
a prescribed burn program (Service
2018, p. 12).
(5) Comment: One commenter stated
that keeping the species listed will
improve the Florida golden aster’s
chances of recovery, adding that
continued listing would provide
support necessary to continue research
and conservation work for the species.
Our response: We agree that the
protections of the Act have helped
recover the Florida golden aster, such
that it no longer meets the Act’s
definition of an endangered species or a
threatened species. Currently, the vast
majority of the known populations
occur on protected and managed
conservation lands and have at least
moderate resiliency. Additionally, we
expect habitat management for the
species to continue, such that these
populations will only increase, though
this was not relied on for the delisting
determination. The Florida golden aster,
therefore, is recovered and no longer
warrants the protections of the Act, now
or in the foreseeable future. Retaining
the species on the Federal List of
Endangered and Threatened Plants
would be contrary to the direction of the
Act and would continue to draw
resources from other species that still
need the protections of the Act.
Background
A thorough review of the taxonomy,
life history, ecology, and overall
viability of the Florida golden aster is
presented in the SSA report available on
https://www.regulations.gov under
Docket No. FWS–R4–ES–2019–0071. A
summary of that information is
presented here.
Florida golden aster is endemic to
xeric (very dry) uplands east and
southeast of the Tampa Bay area of
central Florida. The historical range of
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the Florida golden aster is thought to
span parts of Hillsborough, Manatee,
Pinellas, Highlands, and Hardee
Counties, but the true extent of the
historical range is uncertain because the
ecosystems on which it occurs were
rapidly converted to residential,
commercial, and agricultural uses after
European settlement of the region.
Agriculture began in 1880, with grazing
and production of citrus and row crops.
Residential and commercial activity
began around 1840, mainly in the
Tampa Bay area and beach communities
through the 1940s and 1950s, but
suburban and rural areas started
expanding in the 1960s and 1970s and
that expansion has continued at a
consistent rate. The species was first
collected and described from a
specimen in Manatee County in early
1901, with subsequent collections in
Pinellas and Hillsborough Counties in
the 1920s. The earliest known Manatee
County and Pinellas County populations
occurred in coastal areas of Bradenton
Beach and St. Petersburg Beach.
However, these populations have since
been extirpated. The last remaining
natural population known to occur in
Pinellas County was discovered in 1983;
however, a housing development
eliminated all available habitat by 1985.
When the species was listed as
endangered in 1986 (see 51 FR 17974;
May 16, 1986), nine known extant
populations of the species occurred in
five locations, all coastal, in
southeastern Hillsborough County
(Wunderlin et al. 1981, entire). Since
the listing of the species, increased
survey efforts have resulted in the
discovery of additional populations,
including occurrences farther inland.
Many of the newly discovered locations
have since been acquired as protected
sites with active conservation
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management activities implemented to
improve habitat conditions. As
discussed below, introductions have
occurred on conservation lands in
Hardee, Hillsborough, Manatee, and
Pinellas Counties. It is not known
whether these introduction sites were
historically occupied by the Florida
golden aster or, if so, how long ago they
supported natural populations.
Based on the most current surveys
across the species’ range (2006–2018),
30 known extant populations, natural
and introduced, occur in 5 counties
(Hardee—4 populations, Highlands—1
population, Hillsborough—16
populations, Manatee—5 populations,
and Pinellas—4 populations; figure 1).
Populations were delineated using a
separation distance of 2 kilometers (km)
between occurrences (see Current
Condition, below, for more
information). Of these, 25 populations
occur entirely or mostly on 22 protected
sites; a protected site is a site that has
been acquired in fee simple and placed
into long-term conservation, or that has
a conservation easement or other
binding land agreement by the site
owner that shows a commitment to its
conservation in perpetuity. In addition,
all protected sites have a management
agreement or plan both developed and
implemented. None of the lands
occupied by the Florida golden aster are
federally owned or managed but rather
they are owned and managed by a State,
local, or nongovernmental entity. The
remaining five extant populations occur
on private lands or along roadways or
railroad lines.
The most recent surveys (occurring
between 2006 and 2018) show that just
over half of the Florida golden aster
individuals occur in nine introduced
populations at eight sites. The earliest
introductions, a total of 10, were
undertaken in 1986; three of those
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populations remain extant in Hardee
and Manatee Counties, while seven
other introductions in Pinellas and
Hillsborough Counties failed.
Introductions were again initiated
during 2008–2013, when Bok Tower
Gardens introduced six additional
populations in Hardee, Manatee, and
Pinellas Counties, containing 24,825
plants (as of the most recent censuses,
with about 12,000 in one population).
Four of the six populations contain
more than 1,000 plants; the remaining
two populations (North and South
Duette Preserve) are the most recently
introduced populations (2013), have
been growing rapidly, and are
surrounded by ample habitat and little
to no development, so they will also
reach sizes comparable to the other
introduced populations.
According to the most recent surveys,
approximately 50,000 individuals exist
with more than 90 percent occurring in
the 25 populations located on protected
lands. Although this estimate is the best
available information, it gives only an
approximation of the true current
abundance of the Florida golden aster
because surveys are not conducted
every year and are conducted for
different objectives. Moreover,
population sizes fluctuate annually.
Twelve of the 30 populations had more
than 1,000 individual plants present
when last observed. We note that a 56km gap occurs between the easternmost
naturally occurring population in
Manatee County and the nearest
naturally occurring population in
Hardee County, and it is not presently
known whether this gap is due to the
lack of suitable habitat, lack of
observation, a long-distance dispersal
event, or fragmentation of a formerly
continuous distribution.
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Recovery Criteria
Section 4(f) of the Act directs us to
develop and implement recovery plans
for the conservation and survival of
endangered and threatened species
unless we determine that such a plan
will not promote the conservation of the
species. Under section 4(f)(1)(B)(ii),
recovery plans must, to the maximum
extent practicable, include objective,
measurable criteria which, when met,
would result in a determination, in
accordance with the provisions of
section 4 of the Act, that the species be
removed from listed status.
Recovery plans provide a roadmap for
us and our partners on methods of
enhancing conservation and minimizing
threats to listed species, as well as
measurable criteria against which to
evaluate progress towards recovery and
assess the species’ likely future
condition. However, they are not
regulatory documents and do not
substitute for the determinations and
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promulgation of regulations required
under section 4(a)(1) of the Act. A
decision to revise the status of a species
or to delist a species is ultimately based
on an analysis of the best scientific and
commercial data available to determine
whether a species is no longer an
endangered species or a threatened
species, regardless of whether that
information differs from the recovery
plan.
There are many paths to
accomplishing recovery of a species,
and recovery may be achieved without
all the criteria in a recovery plan being
fully met. For example, one or more
criteria may be exceeded while other
criteria may not yet be accomplished. In
that instance, we may determine that
the threats are minimized sufficiently
and that the species is robust enough
that it no longer meets the Act’s
definition of an endangered species or a
threatened species. In other cases, we
may discover new recovery
opportunities after having finalized the
recovery plan. Parties seeking to
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conserve the species may use these
opportunities instead of methods
identified in the recovery plan.
Likewise, we may learn new
information about the species after we
finalize the recovery plan. The new
information may change the extent to
which existing criteria are appropriate
for identifying recovery of the species.
The recovery of a species is a dynamic
process requiring adaptive management
that may, or may not, follow all the
guidance provided in a recovery plan.
We issued the recovery plan for the
Florida golden aster on August 29, 1988.
The primary objective of the recovery
plan was to provide sufficient habitat
for the Florida golden aster, both
through protection of the sites and
proper vegetation management. The
recovery plan calls for establishment of
new populations of the species. The
recovery plan states that reclassification
of this species to threatened could be
considered if 10 geographically distinct
populations are established in its three
native counties, and delisting could be
E:\FR\FM\05MRR1.SGM
05MRR1
ER05MR24.000
FIGURE 1. The five Florida counties where the Florida golden aster occurs as of2017 are
highlighted in gray, with Hillsborough County shaded darker gray. At the time of listing in 1986,
populations of the Florida golden aster were only known to occur in Hillsborough Country.
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considered if 20 such populations are
secured (USFWS 1988, p. 3). Currently,
Florida golden aster occurs in 30
geographically distinct populations
across five counties, 25 are on protected
lands, and 18 of these populations have
high or very high resiliency (see table 2),
which is consistent with the recovery
plan’s delisting criterion.
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Regulatory and Analytical Framework
Regulatory Framework
Section 4 of the Act (16 U.S.C. 1533)
and the implementing regulations in
Title 50 of the Code of Federal
Regulations set forth the procedures for
determining whether a species is an
endangered species or a threatened
species, issuing protective regulations
for threatened species, and designating
critical habitat for endangered and
threatened species. In 2019, jointly with
the National Marine Fisheries Service,
the Service issued a final rule that
revised the regulations in 50 CFR part
424 regarding how we add, remove, and
reclassify endangered and threatened
species and the criteria for designating
listed species’ critical habitat (84 FR
45020; August 27, 2019). On the same
day, we issued a final rule that revised
50 CFR 17.31 and 17.71 (84 FR 44753;
hereinafter, ‘‘the 20194(d) rule’’) and
ended the ‘‘blanket rule’’ option for
application of section 9 prohibitions to
species newly listed as threatened after
the effective date ofthose regulatory
revisions (September 26, 2019). Blanket
rules had extended the majority of the
protections (all of the prohibitions that
apply to endangered species under
section 9 and additional exceptions to
the prohibitions) to threatened species,
unless we issued an alternative rule
under section 4(d) of the Act for a
particular species (i.e., a species-specific
4(d) rule). The blanket rule protections
continued to apply to threatened species
that were listed prior to September 26,
2019, without an associated speciesspecific rule. Under the 2019 4(d) rule,
the only way to apply protections to a
species newly listed as threatened is
forus to issue a species-specific rule
settingout the protective regulations that
are appropriate for that species. Our
analysis for this decision applied our
current regulations, portions of which
were last revised in 2019. Given that we
proposed further revisions to these
regulations on June 22, 2023 (88 FR
40742; 88 FR 40764), we have also
undertaken an analysis of whether the
decision would be different if we were
to apply those proposed revisions. We
concluded that the decision would have
been the same if we had applied the
proposed 2023 regulations. The analyses
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under both the regulations currently in
effect and the regulations after
incorporating the June 22, 2023,
proposed revisions are included in our
decision file.
The Act defines an endangered
species as a species that is in danger of
extinction throughout all or a significant
portion of its range, and a threatened
species as a species that is likely to
become an endangered species within
the foreseeable future throughout all or
a significant portion of its range. The
Act requires that we determine whether
any species is an endangered species or
a threatened species because of any of
the following 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.
These factors represent broad
categories of natural or human-caused
actions or conditions that could
influence a species’ continued
existence. In evaluating these actions
and conditions, we look for those that
may have a negative effect on
individuals of the species, as well as
other actions or conditions that may
ameliorate any negative effects or may
have positive effects. The determination
to delist a species must be based on an
analysis of the same five factors.
We use the term ‘‘threat’’ to refer in
general to actions or conditions that are
known to or are reasonably likely to
negatively affect individuals of a
species. The term ‘‘threat’’ includes
actions or conditions that have a direct
impact on individuals (direct impacts),
as well as those that affect individuals
through alteration of their habitat or
required resources (stressors). The term
‘‘threat’’ may encompass—either
together or separately—the source of the
action or condition or the action or
condition itself.
However, the mere identification of
any threat(s) does not necessarily mean
that the species meets the statutory
definition of an endangered species or a
threatened species. In determining
whether a species meets either
definition, we must evaluate all
identified threats by considering the
species’ expected response and the
effects of the threats—considering those
actions and conditions that will
ameliorate the threats—on an
individual, population, and species
level. We evaluate each threat and its
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expected effects on the species, then
analyze the cumulative effect of all the
threats on the species. We also consider
the cumulative effect of the threats
considering those actions and
conditions that will have positive effects
on the species, such as any existing
regulatory mechanisms or conservation
efforts. The Secretary determines
whether the species meets the definition
of an endangered species or a threatened
species only after conducting this
cumulative analysis and describing the
expected effect on the species now and
in the foreseeable future.
The Act does not define the term
‘‘foreseeable future,’’ which appears in
the statutory definition of ‘‘threatened
species.’’ Our implementing regulations
at 50 CFR 424.11(d) set forth a
framework for evaluating the foreseeable
future on a case-by-case basis. The term
‘‘foreseeable future’’ extends only so far
into the future as we can reasonably
determine that both the future threats
and the species’ responses to those
threats are likely. In other words, the
foreseeable future is the period of time
in which we can make reliable
predictions. ‘‘Reliable’’ does not mean
‘‘certain’’; it means sufficient to provide
a reasonable degree of confidence in the
prediction. Thus, a prediction is reliable
if it is reasonable to depend on it when
making decisions.
It is not always possible or necessary
to define foreseeable future as a
particular number of years. Analysis of
the foreseeable future uses the best
scientific and commercial data available
and should consider the timeframes
applicable to the relevant threats and to
the species’ likely responses to those
threats in view of its life-history
characteristics. Data that are typically
relevant to assessing the species’
biological response include speciesspecific factors such as lifespan,
reproductive rates or productivity,
certain behaviors, and other
demographic factors.
Analytical Framework
The SSA report documents the results
of our comprehensive biological review
of the best scientific and commercial
data regarding the status of the species,
including an assessment of the potential
threats to the species. The SSA report
does not represent our decision on
whether the species should be
reclassified or delisted under the Act. It
does, however, provide the scientific
basis that informs our regulatory
decisions, which involve the further
application of standards within the Act
and its implementing regulations and
policies.
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To assess Florida golden aster
viability, we used the three conservation
biology principles of resiliency,
redundancy, and representation (Shaffer
and Stein 2000, pp. 306–310). Briefly,
resiliency is the ability of the species to
withstand environmental and
demographic stochasticity (for example,
wet or dry, warm or cold years);
redundancy is the ability of the species
to withstand catastrophic events (for
example, droughts, large pollution
events), and representation is the ability
of the species to adapt to both near-term
and long-term changes in its physical
and biological environment (for
example, climate changes, pathogen). In
general, species viability will increase
with increases in resiliency,
redundancy, and representation (Smith
et al. 2018, p. 306). Using these
principles, we identified the species’
ecological requirements for survival and
reproduction at the individual,
population, and species levels, and
described the beneficial and risk factors
influencing the species’ viability.
The SSA process can be categorized
into three sequential stages. During the
first stage, we evaluated individual
species’ life-history needs. The next
stage involved an assessment of the
historical and current condition of the
species’ demographics and habitat
characteristics, including an
explanation of how the species arrived
at its current condition. The final stage
of the SSA involved making predictions
about the species’ responses to positive
and negative environmental and
anthropogenic influences. Throughout
all these stages, we used the best
available information to characterize
viability as the ability of a species to
sustain populations in the wild over
time. We use this information to inform
our regulatory decision.
The following is a summary of the key
results and conclusions from the SSA
report; the full SSA report can be found
at Docket No. FWS–R4–ES–2019–0071
on https://www.regulations.gov.
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Summary of Biological Status and
Threats
In this discussion, we review the
biological condition of the species and
its resources, and the threats that
influence the species’ current and future
condition, in order to assess the species’
overall viability and the risks to that
viability.
Summary of SSA Analysis
For a species to be viable there must
be adequate redundancy (suitable
number, distribution, and connectivity
to allow the species to withstand
catastrophic events), representation
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(genetic and environmental diversity to
allow the species to adapt to changing
environmental conditions), and
resiliency (ability of a species to
withstand unpredictable disturbance).
Resiliency for Florida golden aster
improves with maintained open habitat.
Lambert and Menges (1996, pp. 121–
137) recommend prescribed burning
that mimics the historic burn pattern
(frequent low-intensity fires in sandhill,
less frequent burns in scrub, with fires
primarily in late spring and summer)
and periodic mechanical disturbance of
the ground cover during late winter or
early spring when seeds are dispersed.
In the absence of fire, habitat openness
can be maintained with mowing, hand
removal of trees and shrubs near plants,
or other mechanical treatments;
populations have persisted along
periodically mowed rights-of-way (e.g.,
underneath powerlines, along roads and
railroads) for decades without a
prescribed burn program. Populations
must be suitably large and connected to
provide a reservoir of individuals for
cross-pollination, as plants will not selffertilize, and to maintain levels of
genetic diversity high enough to prevent
harmful consequences from inbreeding
depression and genetic drift (Ellstrand
and Elam 1993, pp. 217–242).
Redundancy improves with increasing
numbers of populations, and
connectivity (either natural or humanfacilitated) allows connected
populations to ‘‘rescue’’ each other after
catastrophes. Representation improves
with increased genetic diversity and/or
environmental conditions within and
among populations.
Viability of the Florida golden aster
has been and will continue to be
impacted both negatively and positively
by anthropogenic and natural
influences. Historically, the primary
threats to the Florida golden aster were
habitat loss (resulting from human
development) and habitat degradation
due to lack of adequate habitat
management. As threats to habitat have
been alleviated via habitat protection
and management, recovery has been
further bolstered by captive propagation
followed by introduction into
unoccupied sites.
Analysis of Threat Factors
Present or Threatened Destruction,
Modification, or Curtailment of the
Species’ Habitat or Range
The main threat to this species at the
time of listing was the destruction and
modification of habitat. Habitat
destruction, modification, and
degradation on private lands and habitat
degradation from lack of adequate
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habitat management on public lands
remain the primary risk factor to the
species. The five populations occurring
on private lands remain subject to
adverse human activity including
dumping, off-road recreational vehicles
use, and land clearing. However, these
activities are no longer threats to the 25
populations on protected conservation
lands because of controlled access and
restricted use.
Lack of management, especially the
absence of periodic fire, historically led
to habitat degradation throughout the
species’ range. The Florida golden aster
occurs in open, sandy patches that
historically were maintained by fire
under natural conditions. Without
naturally ignited fires or prescribed fire
applications, the habitat becomes
overgrown, resulting in unfavorable
conditions for the species’ persistence.
Ideal habitat management is generally
regarded as prescribed burning that
mimics the historical burn patterns
(frequent low-intensity fires in sandhill,
less frequent burns in scrub, with fires
primarily in late spring and summer)
and periodic mechanical disturbance of
the ground cover during late winter or
early spring when seeds are dispersed
(Lambert and Menges 1996, pp. 121–
137). Initial burning to restore the
openness of degraded habitat involves
frequent intense fires, after which
burning can be less intense and less
frequent to simply maintain the habitat.
Failing to maintain open scrub habitat
can disrupt the Florida golden aster’s
reproduction, survival, and dispersal
(Lambert and Menges 1996, pp. 121–
137).
As with habitat destruction and
modification, this threat from lack of
management remains a concern mainly
on private, non-conservation lands.
Populations that occur on conservation
lands are often being managed to
maintain optimal open scrub habitat.
However, budget constraints,
manageability, conflicting priorities,
and other factors (weather, lack of
equipment, staff shortages, etc.) may
preclude proper management activities
even on conservation lands.
Additionally, proximity to urbanized
areas can limit the number of days
available for prescribed burns, and
urbanization in the Tampa Bay area is
increasing rapidly (Xian et al. 2005, pp.
920–928). To be optimal, burn days
must have wind speeds and wind
directions that do not unduly burden
urbanized areas with smoke. For this
reason, large rural tracts of habitat are
easier to burn than small tracts tucked
into developed areas. Increasing
commercial and residential
development could lead to further
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decreases in the ability to conduct
prescribed burning in the future, which
may or may not be replaced with
adequate habitat management by other
means (e.g., mowing) that are more
expensive than using fire. The type of
development also factors into
management ability and flexibility, with
major roads, schools, hospitals,
retirement homes (places with
vulnerable populations) weighing more
heavily on the decision of if/when to
burn than other types of development
(Camposano 2018, pers. comm.).
Since the time of listing, conservation
efforts for the Florida golden aster and
other scrub habitat species have reduced
the threat of habitat destruction,
modification, and degradation. These
conservation efforts include acquiring
properties where the species naturally
occurs, introducing populations on
conservation lands, and conducting
habitat management on conservation
lands (e.g., prescribed burning). While
habitat destruction and modification
may still occur on private lands, 83
percent of the sites are on public
conservation lands and, therefore, for
the most part, are adequately managed
and protected. Land acquisitions and
introductions have increased the
number of established populations
within the historical range and have
resulted in the expansion of the species’
known range. Further, although the
species will be delisted under the Act
on the effective date of this rule (see
DATES, above), the Florida golden aster
will remain listed as threatened under
State laws. Based on the best available
information, we conclude that resources
for necessary management activities on
conservation lands will continue.
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Disease or Predation
At the time of listing, grazing by
domestic livestock was identified as a
stressor because the species’
populations were on private lands and
many of the properties were in cattle
production. However, at present, the 25
populations on conservation lands are
not subject to any agriculture practices.
No cattle grazing occurs on any of these
properties. Therefore, we no longer
consider grazing to be a threat.
Inadequacy of Existing Regulatory
Mechanisms
The Florida Administrative Code
(FAC) chapter 5B–40 (Preservation of
Native Flora of Florida) provides the
Florida Department of Agriculture and
Consumer Services limited authority to
protect plants on State and private lands
(primarily from the standpoint of illegal
harvest). Florida golden aster is listed as
an endangered plant under this statute,
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which requires anyone wishing to
willfully harvest, collect, pick, remove,
injure, or destroy any plant listed as
endangered growing on the private land
of another, or on any public land or
water, to obtain the written permission
of the owner of the land or water or his
legal representative (FAC 5B–
40.003(1)(a)). A permit is also required
to transport for the purpose of sale,
selling, or offering for sale any plant
contained on the State’s endangered
plant list that is harvested from such
person’s own property (FAC 5B–
40.003(1)(c)). The delisting of the
Florida golden aster under the Act will
not affect this State listing.
Several sites, consisting of thousands
of plants, are now under county and
State protection. Specifically,
Hillsborough County has purchased
considerable acreage through the
Endangered Land Acquisition and
Protection Program (ELAPP) that
contains several large populations of
Florida golden aster. In 1987,
Hillsborough County passed the
Environmentally Sensitive Lands
Ordinance that established the
foundation for ELAPP. This applies to
nine populations on six sites in
Hillsborough County. In 1990, this
ordinance was amended and approved
for another 20 years by increasing
county taxes to allow additional funds
to acquire conservation lands. In
November 2008, voters approved the
issuance of up to $200 million in bonds
for additional purchases.
ELAPP has worked with the
Southwest Florida Water Management
District and Florida Forever to jointly
fund the acquisition of lands. Some of
this money is also used for ELAPP to
actively manage their properties to
benefit Florida golden aster. Therefore,
we find that the existing regulatory
mechanisms will provide sufficient
protections to the species and habitat
after delisting, especially on public
lands with ordinance protection.
Currently, 27 sites where the species
occurs are subject to Florida State law.
These State and local protections have
proven effective. For example,
prescribed burning will continue
through the ELAPP. Although we
acknowledge that this could change in
the future, we do not anticipate any
future changes to the implementation of
these programs at this time.
Other Natural or Manmade Factors
Affecting the Species’ Continued
Existence
Our analyses under the Act include
consideration of ongoing and projected
changes in climate. The terms ‘‘climate’’
and ‘‘climate change’’ are defined by the
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Intergovernmental Panel on Climate
Change (IPCC). A recent compilation of
climate change and its effects is
available from reports of the IPCC (IPCC
2014, entire). 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 2007, p. 78). Various types
of changes in climate can 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 the effects of
interactions of climate with other
variables (e.g., habitat fragmentation)
(IPCC 2007, pp. 8–14, 18–19). In our
analyses, we use our expert judgment to
weigh relevant information, including
uncertainty, in our consideration of
various aspects of climate change.
The IPCC concluded that the climate
system is warming (Pachauri et al. 2014,
entire). Effects associated with changes
in climate have been observed,
including changes in arctic
temperatures and ice, widespread
changes in precipitation amounts, ocean
salinity, and wind patterns and aspects
of extreme weather including droughts,
heavy precipitation, heat waves, and the
intensity of tropical cyclones (Pachauri
et al. 2014, entire). Species that are
dependent on specialized habitat types,
limited in distribution, or at the extreme
periphery of their range may be most
susceptible to the impacts of climate
change (Byers and Norris 2011, entire;
Anacker et al. 2013, pp. 193–210).
However, while continued change is
certain, the magnitude and rate of
change is unknown in many cases and
could be affected by many factors (e.g.,
weather circulation patterns).
According to the IPCC, most plant
species cannot naturally shift their
geographical ranges sufficiently fast to
keep up with current and high projected
rates of climate change on most
landscapes (IPCC 2014, p. 13). Plant
species with restricted ranges may
experience population declines as a
result of the effects of climate change.
The concept of changing climate can be
meaningfully assessed both by looking
into the future and reviewing past
changes.
Using the National Climate Change
Viewer and using greenhouse gas
emission scenario (representative
concentration pathway (RCP) 8.5), we
calculated projected annual mean
changes from 1981–2010 to those
projected for 2025–2049 for maximum
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temperature, precipitation, soil storage,
and evaporative deficit in all counties
where Florida golden aster occurs
(Adler and Hostetler 2017, entire). We
also calculated projected annual mean
changes for a more conservative
greenhouse gas emission scenario (RCP
4.5) using the same timeframes for
maximum temperature, precipitation,
soil storage, and evaporative deficit in
all counties where Florida golden aster
occurs (Adler and Hostetler 2017,
entire). Based on these results, all 5
counties within the range of Florida
golden aster will be subjected to higher
temperatures (annual mean increase of
2.6 degrees Fahrenheit (°F) (RCP 4.5) or
2.9 °F (RCP 8.5)) and slightly higher
precipitation (annual mean increase of
0.1 inch per month (RCP 4.5) or 0.2 inch
per month (RCP 8.5)) in the period of
2025–2049 relative to the period of
1981–2010.
Additionally, climate change will
likely influence Florida golden aster
into the future by affecting habitat
suitability and the ability to manage
habitat with prescribed fire. Species that
are dependent on specialized habitat
types, limited in distribution (e.g.,
Florida golden aster), or at the extreme
periphery of their range may be most
susceptible to the impacts of climate
change (Byers and Norris 2011, entire;
Anacker et al. 2013, pp. 193–210). There
is evidence that some terrestrial plant
populations have been able to adapt and
respond to changing climatic conditions
(Franks et al. 2014, pp. 123–139). Both
plastic (phenotypic change such as leaf
size or phenology) and evolutionary
(shift in allelic frequencies) responses to
changes in climate have been detected.
Given enough time, plants can alter
their ranges, resulting in range shifts,
reductions, or increases (Kelly and
Goulden 2008, pp. 11823–11826; Loarie
et al. 2008, p. 2502).
The climate in the southeastern
United States has warmed about 2 °F
from a cool period in the 1960s and
1970s and is expected to continue to
rise (Carter et al. 2014, pp. 396–417).
Projections for future precipitation
trends in the Southeast are less certain
than those for temperature, but suggest
that overall annual precipitation will
decrease, and that tropical storms will
occur less frequently, but with more
force (e.g., more category 4 and 5
hurricanes) than historical averages
(Carter et al. 2014, pp. 396–417).
Climatic changes, including sea level
rise (SLR) and shifts in seasonal
precipitation, temperature, and storm
cycles, are projected to impact the
southeastern United States over the next
century. Under both lower and higher
emissions scenarios, temperatures are
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expected to increase (Carter et al. 2018,
pp. 751–752), and climate change is
expected to intensify the hydrologic
cycle and increase the frequency and
severity of extreme events like drought
and heavy rainfall (Carter et al. 2018, p.
775). Increases in evaporation of
moisture from soils and loss of water by
plants in response to warmer
temperatures are expected to contribute
to increased frequency, duration, and
intensity of droughts. Local sea level
rise impacts depend not only on how
much the ocean level itself is increasing,
but also on land subsidence and/or
changes in offshore currents (Carter et
al. 2014, pp. 396–417), and impacts on
terrestrial ecosystems can occur via
submergence of habitat during storm
surges or permanently, saltwater
intrusion into the water table, and
erosion. Of the current populations of
the Florida golden aster, only one (Fort
De Soto County Park, Pinellas County)
is directly vulnerable to inundation
from 0.3 m of sea level rise, a reasonable
estimate of sea level rise by 2050. Hotter
and drier conditions in the future could
lead to fewer days with optimal
conditions for prescribed burning,
which could lead to reduced habitat
quality if land managers are unable to
make up for the lack of burning with
adequate mechanical treatment.
It is possible that there will be
increases in the number of lightning
strikes and sizes and severities of
resulting fires, which could have a
positive or negative effect on specific
Florida golden aster populations.
Hurricanes similarly could have
positive or negative effects on the
species. Prolonged flooding could harm
populations, but the mechanical
disturbance of trees being uprooted from
flood events could improve habitat for
colonizing species like the Florida
golden aster (Menges and Johnson 2017,
pers. comm.).
Other potential climate change effects
include changes in temperature and
precipitation. Projections for future
precipitation trends in the Southeast are
less certain than those for temperature
but suggest that overall annual
precipitation will decrease. Hotter and
drier conditions may complicate the
ability to manage Florida golden aster
with prescribed fires. Some terrestrial
plant populations have been able to
adapt and respond to changing climatic
conditions (Franks et al. 2014, entire).
Both plastic (phenotypic change such as
leaf size or phenology) and evolutionary
(shift in allelic frequencies) responses to
changes in climate have been detected.
Both can occur rapidly and often
simultaneously (Franks et al. 2014,
entire). However, relatively few studies
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are available that (1) directly examine
plant responses over time, (2) clearly
demonstrate adaptation or the causal
climatic driver of these responses, or (3)
use quantitative methods to distinguish
plastic versus evolutionary responses
(Franks et al. 2014, entire).
As noted earlier, only one population
(Fort De Soto County Park, Pinellas
County) is directly vulnerable to
inundation from 0.3 meters of sea level
rise, a reasonable estimate of sea level
rise by 2050. Hotter and drier conditions
in the future could lead to fewer days
with optimal conditions for prescribed
burning, which could lead to reduced
habitat quality if land managers are
unable to make up for the lack of
burning with adequate mechanical
treatment. It is possible that there will
be increases in the number of lightning
strikes and sizes and severities of
resulting wildfires, which could have a
positive or negative effect on specific
Florida golden aster populations.
Hurricanes similarly could have
positive or negative effects on the
species. Prolonged flooding could harm
populations, but the mechanical
disturbance of trees being uprooted
could improve habitat for colonizing
species like Florida golden aster
(Menges and Johnson 2017, pers.
comm.). We have no additional
information or data regarding effects of
climate change with respect to Florida
golden aster populations into the future;
further research will be helpful to
determine how this species responds
directly to changes in temperature and
water availability. However, from the
known and forecasted information, we
anticipate that effects to Florida golden
aster from climate change will be
limited and will not rise to the level of
a threat.
Other influences not discussed in
detail here, either because they are not
thought to be a major threat or there is
little information available, include
invasive plant species like cogongrass
(Imperata cylindrica), and future genetic
consequences of small and/or
translocated populations.
Synergistic Effects
Many of the stressors discussed in
this analysis could work in concert with
each other and result in a cumulative
adverse effect to Florida golden aster,
e.g., one stressor may make the species
more vulnerable to other threats.
Synergistic interactions are possible
between effects of climate change and
effects of other threats, such as mowing,
dumping, off-road recreational vehicle
use, and land clearing. However, we
currently do not have information to
determine the likely effects of climate
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change on interaction/competition
between species, or on drought
conditions. Uncertainty about how
different plant species will respond
under a changing climate makes
projecting possible synergistic effects of
climate change on Florida golden aster
speculative. However, the increases
documented in the number of
populations since the species was listed
do not indicate that cumulative effects
of various activities and stressors are
affecting the viability of the species at
this time. Based on our analysis of
future stressors, we do not anticipate
that cumulative effects will affect the
viability of the species in the foreseeable
future. Likewise, climate change, as
discussed above, with hotter and drier
conditions can add additional
complexity to future prescribed burns.
Available habitat in those tracts that are
easier to burn, or that can be managed
by other methods (e.g., mechanical
manipulation), will be sufficient.
Similarly, most of the potential stressors
we identified either have not occurred
to the extent originally anticipated at
the time of listing or are adequately
managed as described above. In
addition, we do not anticipate
significant stressors to increase on
publicly owned lands or lands that are
managed for the species.
Current Condition
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Delineating Populations
For the SSA, we delineated
populations using a 2-km separation
distance rule based on species expert
opinion, resulting in 30 populations
across five counties. This strategy differs
from the 1-km separation distance rule
that was used in the most recent 5-year
review, which was based on
NatureServe’s default criteria for
defining plant populations (NatureServe
2004, entire). The team of species
experts providing input on the SSA
suspected that 1 km is likely an
underestimate of the distance that gene
flow can regularly occur via pollination.
While the exact insect pollinators of the
Florida golden aster are not known,
studies on multiple bee species (major
plant and Chrysopsis pollinators)
demonstrate foraging distances that
regularly exceed 1 km (Greenleaf et al.
2007, pp. 289–296; Hagler et al. 2011, p.
144).
Current Resiliency
Resiliency refers to the ability of
populations to withstand stochastic
events, whether demographic,
environmental, or anthropogenic.
Populations with low resiliency are
highly vulnerable to stochastic events
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and face a high risk of extirpation
within the next few decades.
Populations with moderate resiliency
are less likely to be extirpated within
the next few decades, but require
additional growth (with help of regular
habitat management and/or restoration)
to become more self-sustaining and
resilient to stochastic events.
Populations with high resiliency are
unlikely to be extirpated within the next
30 years in the absence of catastrophes
or significant declines in the quality of
habitat management. Populations with
very high resiliency are the most robust
and resistant to stochastic fluctuations.
In the SSA, we assessed resiliency for
each population using three factors: (1)
population size, (2) habitat protection,
and (3) area of available habitat. Other
factors were considered that likely
contribute to population resiliency, but
data were not available to assess them
over all or most of the populations
including certain explicit measures of
habitat quality, fire management,
existence of land management plans,
and population trends. While some past
survey data are available for many
populations, species experts did not feel
comfortable comparing population
counts across time periods. In many
cases, differences in population sizes
were likely not a result of increasing
populations, but rather of differences in
survey methodology, number of
surveyors, and/or areas searched (e.g.,
surveyors who were more likely to visit
known patches and not find new
patches; alternately, a bias toward larger
counts over time as old patches are
revisited and additional patches are
found). Nevertheless, we are confident
that these population data demonstrate
resiliency of the species. Regardless,
this species has not been extensively
studied; therefore, there was some
uncertainty in the SSA in precisely how
these factors influenced Florida golden
aster population resiliency.
Population Size
Population size is both a direct
contributor to resiliency and an indirect
indicator of resiliency. Small
populations are more susceptible to
demographic and environmental
stochastic events than larger
populations. Small populations are also
more likely to suffer from decreased
fitness because of low genetic diversity
from inbreeding or genetic drift (Willi et
al. 2005, pp. 2255–2265). For Florida
golden aster, large populations are more
buffered from the effects of prescribed
burning or other disturbances, which
are necessary to maintain open habitat
but can temporarily reduce population
sizes by killing plants. Indirectly, large
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population sizes are likely indicative of
other conditions that contribute to
population resiliency. For example, in
the SSA, we did not have adequate data
to assess habitat quality and the quality
of management at all the Florida golden
aster populations; therefore, we
assumed large population sizes likely
generally reflect good habitat quality
and management (among other factors)
compared to smaller populations,
although this assumption may not hold
in all cases.
We categorized populations into 4
size classes: fewer than 100 individuals,
100–500 individuals, 501–1,000
individuals, and more than 1,000
individuals. Each population size class
was associated with one of the following
baseline resiliency classes, respectively:
low, moderate, high, and very high
(explained further below).
We chose the population size
threshold between high and very high
resiliency of 1,000 individuals because
it is the typical population size used to
rank element occurrences as having
‘‘excellent viability’’ and likely to
persist for the next 20–30 years
(NatureServe 2008, entire). This is a
generic population size limit that was
not specifically tailored to Florida
golden aster with empirical data.
Further support for using 1,000
individuals as the threshold for the
highest resiliency category came from a
study of 10-year extirpation rates for
populations of varying sizes of eight
short-lived plant species in Germany
(Matthies et al. 2004, pp. 481–488). In
this study, for seven of eight species, the
probability of population persistence
increased with population size, and all
populations of more than 1,000
individuals (flowering plants) persisted
for the duration of the 10-year study.
We obtained the most recent size data
for all 30 populations, with data
collected as recently as 2018 for some
populations, and none older than 2006
for any population. However,
population sizes have undoubtedly
changed since the most recent surveys,
as populations fluctuate in response to
management actions, time since
management, environmental events,
stochastic demographic processes, and
so forth. Thus, the reported numbers
reflect best available estimates for
population sizes, rather than precise
counts meant to represent actual current
population sizes. According to the SSA
report, population sizes include all
plants counted, whether flowering or
not. Survey data for some populations
provide separate counts for each life
stage, but for many populations, survey
data are simply numbers with no
information about whether that number
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was only flowering plants, or all plants
(Service 2018, p. 22). Using total plant
numbers, and assuming that ambiguous
counts are minimum counts of total
plants in each population, we were
conservative in our population counts.
The alternative of assuming that
ambiguous counts are of only flowering
adult plants, when they may include
basal rosettes, would inflate population
sizes in cases where the assumption was
wrong.
Habitat Protection
Habitat was considered ‘‘protected’’ if
it was acquired in fee simple and placed
into long-term conservation by a
nongovernmental, local, State, or
Federal entity, or if there is a binding
land agreement. Protected sites have
management plans developed and being
implemented. The effect of the degree of
habitat protection on resiliency is
discussed below.
Habitat Area Available
Florida golden aster population sizes
fluctuate and can occur in high
densities in small patches of habitat.
However, as a general rule of thumb for
a given population size, a population
covering a large area will be more
resilient than a population covering a
small area. A perturbation of the same
size will have a proportionally larger
effect on small-area populations than
large-area populations. In assessing
population resiliency, we considered
the amount of habitat available rather
than the amount of habitat occupied for
two reasons. First, the amount of area
occupied was very uncertain for most
populations. Surveys are likely to return
to known patches of the Florida golden
aster, but new patches can be easily
missed, and it is likely that the data we
have underestimates the true amount of
area occupied by the Florida golden
aster. Adding to the uncertainty, the
most current spatial data for some
populations comes from 2006, and may
no longer reflect the current distribution
at those sites. Second, population
footprints are not always static across
available habitat; the Florida golden
aster can spread into unoccupied areas
as populations grow, or shift across a
landscape as different areas become
more or less suitable or both. For this
reason, we used the amount of habitat
available for populations to occupy
currently, grow into, or shift into as a
factor contributing to population
resiliency. We identified available
habitat within a 2-km radius around
known occurrences, consistent with the
assumption we made about pollinator
movement when delineating
populations. We characterize the
available habitat for populations as
small or large, with 14.2 hectares as the
threshold between the two groups. This
value was selected based on natural
breaks in the data and expert input.
Classifying Resiliency Based on the
Selected Factors
Resiliency classes were based
primarily on population size as
described above, with four resiliency
classes corresponding to four
population size categories. Populations
with fewer than 100 individuals were
determined to have low resiliency.
Within the three higher population size
categories (100–500, 501–1,000, and
more than 1,000 plants), populations
were assigned a baseline resiliency
score associated with their population
size (moderate, high, or very high,
respectively). This baseline score could
then be lowered by either of the two
other factors, habitat protection and
habitat area available; see table 1 below.
TABLE 1—STRATEGY FOR ASSIGNING CURRENT RESILIENCY SCORES TO POPULATIONS OF C. FLORIDANA
Population size
(# plants)
Habitat protected
Habitat not protected
<100 .........................................................
100–500 ...................................................
501–1,000 ................................................
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>1,000 ......................................................
Low
Low ..........................................................
Moderate ..................................................
Moderate ..................................................
High ..........................................................
High ..........................................................
Very High .................................................
Populations that occur on nonprotected lands were assigned to the
resiliency class one step lower than they
would if they were on protected lands.
By doing this, we did not intend to
discount the importance of populations
on non-protected lands to the viability
of the species or imply that owners of
these parcels are managing the land
poorly or are harming the Florida
golden aster. Large populations of
Florida golden aster can be supported
on private lands. For example, when
private landowners burn pasture to
improve forage for cattle, they may
improve habitat for Florida golden aster.
However, even large populations of fireadapted scrub plants can rapidly
decline due to poor management (e.g.,
Polygal lewtonii, Weekley and Menges
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Small.
Large.
Low ..........................................................
Low ..........................................................
Moderate ..................................................
Moderate ..................................................
High ..........................................................
High ..........................................................
2012, entire; Warea carteri, QuintanaAscenscio et al. 2011, entire), and
private lands that are not protected for
conservation are at higher risk of
changes in management or land use that
could harm Florida golden aster
populations. For populations that
extend across property boundaries and
contain individuals occurring on both
protected and non-protected lands, we
used the protection status that applied
to most individuals to classify the entire
population.
Populations occupying or surrounded
by a small area of available habitat were
assigned to the resiliency class one step
lower than they would otherwise be
assigned if they existed within a larger
area of available habitat, as they are less
able to withstand and recover from
perturbations or shift across a landscape
Habitat area
available
Small.
Large.
Small.
Large.
Small.
Large.
as habitat quality changes. For any
populations experiencing both
resiliency-reducing conditions (small
habitat area on non-protected lands), the
resiliency score was only reduced one
step rather than being reduced twice
(i.e., once for each condition). The
Duette populations were the most
recently introduced populations. They
have been growing rapidly and are
surrounded by ample habitat and little
to no development; therefore, these two
populations were projected to increase
from high to very high resiliency.
Summaries of the 30 delineated
populations and their resiliency scores
can be found in the SSA report (Service
2018, p. 32) and in table 2, below. In
conclusion, resiliency scores remained
stable.
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TABLE 2—SUMMARY OF CURRENT RESILIENCY SCORES BY PROTECTED STATUS FOR FLORIDA GOLDEN ASTER
Resiliency class
All populations
Very High .........................................................................................................................
High ..................................................................................................................................
Moderate ..........................................................................................................................
Low ..................................................................................................................................
Current Redundancy and
Representation
Redundancy for Florida golden aster
is naturally low because it is an
endemic species with a narrow range in
Florida around the Tampa Bay region
and Hardee County farther inland (with
one population just across the border in
Highlands County). The entire species’
range spans five counties, with half of
the populations occurring in
Hillsborough County (see figure 2,
below). The longest distance between
two populations is 131 km. However, as
this is a narrow-ranging endemic, the
spatial distribution of populations
across its range does confer a moderate
amount of redundancy, defined as the
ability of the species to withstand
catastrophic events. Catastrophic events
could include, among others, fires
occurring too frequently, droughts,
disease outbreaks, or hurricanes with
prolonged flooding, each of which have
Protected
7
11
6
6
impacts at a different spatial scale. No
information is known about seedbank
resiliency in the soil for this species;
without knowing this, it is difficult to
predict long-term impacts of
catastrophes.
The 30 known populations are
distributed in three main groupings.
There are about 20–30 km between each
of the groupings, providing a buffer
around each that may protect them from
catastrophic events affecting the others
(e.g., disease outbreak, depending on
transmission type and vectors). Within
each geographic cluster, there are at
least two highly or very highly resilient
populations, which could serve as
sources to naturally recolonize
populations lost to catastrophic events.
The Hardee-Highlands cluster has the
lowest redundancy (two moderately
resilient populations, six populations
total) and is the most isolated from the
other clusters. The Pinellas cluster has
the next lowest redundancy of resilient
Not protected
7
10
5
3
0
1
1
3
populations (3 highly resilient
populations, 4 populations total), and
the Hillsborough-Manatee cluster has
the highest redundancy (13 resilient
populations, 20 populations total); see
figure 2 below. Another factor
contributing to redundancy is the wide
range of property ownership; with so
many managing entities, the species is
buffered against poor management of
any one entity (e.g., due to budget issues
or changing priorities). Based on the
spatial distribution of resilient
populations managed by a variety of
entities across a narrow range, current
redundancy is considered qualitatively
to be low to moderate. Rather than
solely relying on this rather subjective
classification in assessing the current
viability of the species, characterizing
current redundancy is most useful in
comparison to redundancy under the
future scenarios; see Future Conditions
discussion below.
Hillsborough
Highlands
N
Kilometers
FIGURE 2. Spatial distribution of Florida golden aster populations in three main geographic
clusters across five counties in Florida. The number of populations with high and very high
resiliency is shown within each cluster.
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Representative units for this species
could not be defined based on available
data, with representation defined as the
ability of the species to adapt to
changing environmental conditions.
Species experts contributing to the SSA
suspect that there might be
representative units with different
genetic adaptations associated with soil
differences, elevation above the water
table, fire regime, or habitat structure.
However, there are no data currently to
confirm or refute these hypotheses.
Genetic studies have found little to no
genetic clustering among populations,
with 80 percent of observed genetic
variation occurring within populations,
and only 20 percent of the variation
attributable to between-population
differences (Markham 1998, p. 41).
These results support the existence of a
single representative unit for the
species. However, that study did not
examine genetic markers known to be
associated with adaptive traits. Vital
rates and morphology were observed to
differ between individuals from
different source populations that were
grown at Bok Tower Gardens and
introduced to other sites (Campbell
2008, entire). This observation provides
evidence that there might be adaptive
differences between different ‘‘types’’ of
the Florida golden aster across the
species’ range. However, without any
firm evidence to define representative
units, we refrain from doing so here.
Future research on the Florida golden
aster’s genetics, life history, and habitat
differences can provide a more
definitive basis for defining
representative units in future iterations
of the SSA report.
Future Conditions
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Analytical Framework
For the SSA report, we developed
three plausible future scenarios under
which to capture the breadth of all
likely future variability and assess the
future viability of Florida golden aster
in terms of resiliency, redundancy, and
representation. Based on expert opinion,
the lifespan of the Florida golden aster,
ideal fire-return intervals (at least every
10 years), uncertainty about future
conditions, and lack of knowledge about
certain aspects of Florida golden aster
ecology, we chose to project populations
20 years into the future under each
scenario, although some of these
projections could be reasonably
expected to continue for some time after
the 20 years. With approximately 30
years of real data and trends, we project
that the same trends will continue. The
three hypothetical future scenarios are
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Status Quo, Pessimistic, and Targeted
Conservation.
In considering development as a
threat, we used the SLEUTH (Slope,
Land use, Excluded, Urban,
Transportation and Hillshade; Jantz et
al. 2010, p. 34:1–16) data sets from the
years 2020 (closest to current year) and
2040 (closest to 20 years in the future),
and examined the area predicted, with
at least 80 percent probability, to be
urbanized. Therefore, our assessment
was both quantitative, calculating the
area within the 5-km buffer surrounding
each population that was urbanized at
each time point, and qualitative,
inspecting the distribution of
urbanization and major roads within
that area (e.g., is the urbanization
concentrated to one side of the
population or surrounding it).
With both the quantitative and
qualitative assessments, we categorized
populations as having either low risk or
high risk of development impacting
management for Florida golden aster.
We defined high risk of impacting
management as greater than 50 percent
chance of negatively impacting
management, and less than 50 percent
for low risk. Populations classified as
having low risk from development
averaged 7.9 percent developed area
within the 5-km buffer by 2040, with a
range of 0 to 39 percent developed.
Populations classified as having high
risk from development averaged 45.5
percent developed area within the same
buffer, ranging from 23 to 85 percent.
For three populations with a percent of
developed area in the overlapping range
between the two categories (23 to 39
percent developed), the deciding factor
between low risk and high risk was the
distribution of development and roads
around the population.
Habitat Quantity
Habitat quantity can be negatively
impacted by development or land use
change (particularly on private lands) or
positively impacted by land acquisition,
restoration, and introductions into
unoccupied sites that already have
presumably suitable habitat.
Habitat Quality
Habitat quality is closely tied to active
habitat management to maintain
openness either by prescribed burning
or by other types of management. In
constructing our scenarios, we
considered two avenues by which future
habitat management can be influenced:
(1) the level of habitat management
effort and (2) the amount and type of
development near the Florida golden
aster populations (to the extent the
development affects the ability to
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15775
conduct management actions, such as
prescribed burns). First, the managing
entities can choose their desired level of
management effort by implementing (or
not) a management plan or by allocating
funding or personnel to or away from
habitat management among competing
priorities and limited resources. For our
scenarios, we allowed for three levels of
habitat management effort by managing
entities. The first was management for
stability, a moderate level of
management that would be expected to
maintain populations at their current
size. The other two management levels
were an increase, or a decrease,
compared to management for stability.
An increase in management effort
would be expected to grow populations,
while a decrease in management would
be expected to result in population
declines.
The second avenue by which future
habitat management can be influenced
is development, particularly major roads
and types of development associated
with ‘‘vulnerable’’ human populations
(e.g., schools, hospitals). This kind of
development surrounding habitat limits
management via prescribed burns by
limiting the days that burns can take
place—weather conditions must align to
ensure proper smoke management. For
example, if a population is surrounded
by nearby development to the north and
west, it can only be burned when the
wind is blowing to the south and east.
As more development surrounds
populations, there is less flexibility for
prescribed burns. However, the
appropriate radius around populations
within which development might
impact management ranges from 0.8 km
up to 8.0 km as the appropriate radius
depends on a variety of factors for each
burn, including the type of
development, temperature, humidity,
wind conditions, size of the planned
burn, risk tolerance of those
implementing the burn, and other
factors. For the SSA, we chose an
intermediate value, 5 km, in which to
examine current and predicted future
development. In choosing this concrete
value, we acknowledged that this
number is quite variable, and some
burns will need to consider areas greater
or less than 5 km away, but this value
allowed us to gain a general
understanding of the risks of
development on managing surrounding
populations.
Within a 5-km radius around the
Florida golden aster occurrences, we
used geographic information systems
(GIS) to examine current and projected
urbanization and roads. Urbanization
data came from the SLEUTH model, and
road data were available from the
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Florida Department of Transportation.
The SLEUTH model has previously
been used to predict probabilities of
urbanization across the southeastern
United States in 10-year increments,
and the resulting GIS data are freely
available (Belyea and Terrando 2013,
entire). For our 20-year future
projection, we used the SLEUTH data
sets from the years 2020 and 2040, and
examined the area predicted, with at
least 80 percent probability, to be
urbanized. Our assessment was both
quantitative, calculating the area within
the 5-km buffer surrounding each
population that was urbanized at each
time point, and qualitative, inspecting
the distribution of urbanization and
major roads within that area (e.g., is the
urbanization concentrated to one side of
the population or surrounding it?). With
this quantitative and qualitative
assessment, we categorized populations
as having either a low risk or a high risk
of development impacting the ability to
manage the population.
These two aspects of future
management, (1) management resources
and willingness of the entity to manage,
and (2) impacts of surrounding
development on management,
interacted in our future scenarios in the
following way: with decreases in
management effort (compared to
management for stable populations),
population resiliency decreased one
level. With management for stability,
population resiliency stayed the same as
the current condition resiliency when
there was low risk of development
impacts; but where there was a high
risk, resiliency decreased one level,
reflecting that management will be more
challenging with higher risk from
development. With increases in
management effort, population
resiliency increased when there was low
risk of development impacts, but stayed
the same when there was a high risk; the
increased management effort canceled
out the increased risk caused by
development.
Future Scenarios
Status Quo
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Under the Status Quo scenario, no
new protected areas were acquired and
no new populations were introduced.
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Management efforts for all populations
were maintained at current levels,
assuming that the ability to manage
would not be hampered climate change
or other factors. This scenario also
assumes that conservation commitments
outlined in management plans currently
being implemented will continue. Of
the introductions since 2008, all have
more than 1,000 plants except for the
two populations at Duette Preserve
(North and South).
Pessimistic
Under the Pessimistic scenario,
management effort on all populations
decreased, resulting in a drop in
resiliency scores across the board.
Additionally, based on uncertainty in
whether populations on non-protected
lands would continue to be managed in
a way that is compatible with continued
Florida golden aster persistence, in this
scenario all populations on nonprotected lands were assumed to be lost
due to presumed land use or
management change. As with the Status
Quo scenario, no new protected areas
were acquired, and no new populations
were introduced.
Targeted Conservation
Under the Targeted Conservation
scenario, populations with high and
very high resiliency were managed to
maintain their rank. In cases where
populations had a high risk of
development limiting the ability to
manage, this goal involved an increase
in management effort compared to what
would be needed to maintain the same
level of resiliency for a population with
a low risk of development impacts.
Populations with currently moderate
resiliency on protected lands received
management effort increases to either
move them into the high resiliency class
(low risk from development) or
maintain moderate resiliency (high risk
from development). Conservation
resources were steered towards
maintaining and growing these larger
populations, and not as much towards
rescuing populations that currently have
low resiliency. Additionally, five new
sites were selected across the species’
range in which to introduce new
populations, thus improving species
redundancy.
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Likelihood of Scenarios
Of these three scenarios, the Status
Quo scenario is the most likely to occur,
although the Targeted Conservation
scenario represents a likely future if
both habitat-focused management
(prescribed burning and mechanical or
manual habitat management) by a
variety of partners/managing entities
and species-specific conservation
(captive propagation and introductions)
are prioritized and well-funded. The
Pessimistic scenario was unlikely; given
that Florida golden aster populations
span so many different ownerships, it is
unlikely that all the different managing
entities will develop the land especially
when there are other co-occurring
endangered, threatened, and candidate
species occupying the same habitat (e.g.,
Florida scrub-jay, Aphelocoma
coerulescens; eastern indigo snake,
Drymarchon couperi;. The Targeted
Conservation scenario was not likely
with current conservation resources but,
as noted above, could reflect a likely
future if the needed management and
conservation actions are prioritized and
well-funded.
Future Resiliency
Future (20 years) resiliency of Florida
golden aster populations under three
scenarios is summarized in the SSA
report (Service 2018, p. 49), and is
presented below in table 3. As implied
by the scenario name, resiliency of
populations under the Pessimistic
scenario was predicted to be poor, with
only 7 highly resilient populations, a
decrease from 18 currently highly or
very highly resilient populations. Under
the Status Quo scenario, we expect
resiliency to drop to 12 highly or very
highly resilient populations due solely
to the effect of development limiting the
ability to adequately manage habitat.
Under the Targeted Management
scenario, focused management and
conservation efforts to counteract
detrimental effects of urbanization, the
growth of existing populations, and the
introduction of new populations are
expected to result in significant gains in
resilient populations, with an increase
from 18 to 27 highly or very highly
resilient populations expected highly or
very highly resilient populations.
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TABLE 3—SUMMARY OF RESILIENCY SCORES TALLIED ACROSS ALL POPULATIONS OF FLORIDA GOLDEN ASTER FOR THE
CURRENT CONDITION AND FUTURE CONDITION UNDER THREE HYPOTHETICAL SCENARIOS: STATUS QUO, PESSIMISTIC, AND TARGETED CONSERVATION
Resiliency class
Current
Very High .........................................................................................................
High ..................................................................................................................
Moderate ..........................................................................................................
Low ..................................................................................................................
Likely Extirpated ..............................................................................................
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Future Redundancy and Representation
Redundancy 20 years in the future
was expected to decrease compared to
current condition under the Status Quo
and Pessimistic Scenarios. In all
scenarios, the majority of highly and
very highly resilient populations were
found in Hillsborough and Manatee
Counties. All redundancy of highly
resilient populations in Pinellas County
and the Hardee and Highlands Counties
cluster is lost under the Pessimistic
scenario. In the Status Quo scenario,
where drops in resiliency were due to
development risks to management, no
highly resilient populations remained in
the heavily urbanized Pinellas County.
Even in the Targeted Conservation
scenario, redundancy within Pinellas
County did not improve, but both the
number and distribution of highly
resilient populations in the other two
clusters did improve. We did not assess
representation in the future due to a
present lack of information needed to
delineate representative units.
We note that, by using the SSA
framework to guide our analysis of the
scientific information documented in
the SSA report, we have analyzed the
cumulative effects of identified threats
and conservation actions on the species.
To assess the current and future
condition of the species, we evaluate the
effects of all the relevant factors that
may be influencing the species,
including threats and conservation
efforts. Because the SSA framework
considers not just the presence of the
factors, but to what degree they
collectively influence risk to the entire
species, our assessment integrates the
cumulative effects of the factors and
replaces a standalone cumulative-effects
analysis.
Conservation Efforts and Regulatory
Mechanisms
The Florida Administrative Code 5B–
40 (Preservation of Native Flora of
Florida) provides the Florida
Department of Agriculture and
Consumer Services (FDACS) limited
authority to protect plants on State and
private lands (primarily from the
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Status quo
7
11
6
6
0
standpoint of illegal harvest). Florida
golden aster is listed as an Endangered
Plant under this statute, which requires
anyone wishing to ‘‘willfully harvest,
collect, pick, remove, injure, or destroy
any plant listed as endangered growing
on the private land of another or on any
public land or water’’ to ‘‘obtain the
written permission of the owner of the
land or water or his legal
representative’’ (FAC 5B–40.003(1)(a)).
A permit is also required to transport
‘‘for the purpose of sale, selling, or
offering for sale any plant contained on
the endangered plant list which is
harvested from such person’s own
property’’ (FAC 5B–40.003(1)(c)).
There are now several sites and
thousands of plants under county and
State protection. Specifically,
Hillsborough County has purchased
considerable acreage through the
Endangered Land Acquisition and
Protection Program that contain several
large populations. Golden aster is also
documented at Lake Manatee State
Recreation Area and Little Manatee
River State Park in Manatee and
Hillsborough Counties. Currently, 27
sites where the species occurs are
subject to State laws.
Determination of Florida Golden
Aster’s Status
Section 4 of the Act (16 U.S.C. 1533)
and its implementing regulations (50
CFR part 424) set forth the procedures
for determining whether a species meets
the definition of an endangered species
or a threatened species. The Act defines
an endangered species as a species that
is in danger of extinction throughout all
or a significant portion of its range, and
a threatened species as a species that is
likely to become an endangered species
within the foreseeable future throughout
all or a significant portion of its range.
The Act requires that we determine
whether a species meets the definition
of an endangered species or a threatened
species because of any of the following
factors: (A) The present or threatened
destruction, modification, or
curtailment of its habitat or range; (B)
Overutilization for commercial,
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4
8
11
3
4
Pessimistic
0
7
11
5
7
Targeted
conservation
9
18
2
2
4
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.
Status Throughout All of Its Range
After evaluating threats to the species
and assessing the cumulative effect of
the threats under the Act’s section
4(a)(1) factors, we find that the present
or threatened destruction, modification,
or curtailment of Florida golden aster
habitat (Factor A), which was the basis
for listing the species, is no longer a
threat. At the time of listing, Florida
golden aster was thought to persist only
in Hillsborough County. Now, the
species is known to occur in four
additional counties: Hardee, Highlands,
Mantee, and Pinellas Counties. While
destruction and modification of habitat
is still the primary threat to the species,
the magnitude of this threat has been
greatly reduced since listing. Further,
the number of populations has
increased. Under the recovery plan for
the species, delisting could be
considered if 20 populations were
secured. The number of known extant
populations has increased from 9 in
1986 to 30 in 2017 because of additional
surveys, habitat restoration, and
outplanting within the historical range
of the species. Of those 30 populations,
25 populations are located on protected
conservation lands, and 22 of those 25
populations have been determined to
have at least moderate resiliency. We
expect current levels of management to
continue these conservation lands at
these locations, and we anticipate the
number of individuals within the
populations to increase.
For the determination of whether the
species is likely be become endangered
within the foreseeable future throughout
all its range, and thus meet the Act’s
definition of a threatened species, we
considered the ‘‘foreseeable future’’ to
be 20 years into the future under the
three hypothetical future scenarios. Our
SLEUTH tool projected future possible
development to 20 years, NatureServ
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considers large population sizes likely
to persist over the next 20–30 years, and
considerations of climate change make
projections beyond 20 to 30 years much
more speculative. Also, given the
average lifespan of the species
(approximately 3–5 years), a period of
20 to 30 years allows for multiple
generations and detection of any
population changes. Under all three
scenarios evaluated, the Florida golden
aster is expected to continue to persist
across its currently known range. Under
the Status Quo scenario, which is also
the most likely to occur, 12 populations
are projected to be highly or very highly
resiliency and 11 moderately resilient
across all three geographic clusters, as
habitat modification is no longer a
threat for the populations on protected
lands and current management of those
lands is expected to continue. Four
populations (three natural and one
introduced) currently in low condition
are projected to become extirpated in
the Status Quo scenario. Even under the
Pessimistic scenario, which is least
likely to occur, 7 populations are
projected to be in high condition and 11
in moderate condition, all of which
occur on protected lands with
conservation management expected to
continue at some level. Given that most
populations projected to remain extant
with at least moderate resiliency are on
protected lands managed for scrub
habitat, it is unlikely the species will
become endangered within the
foreseeable future throughout all its
range. Thus, after assessing the best
available information, we conclude that
the Florida golden aster is not in danger
of extinction now or likely to become so
within the foreseeable future throughout
all its range.
Status Throughout a Significant Portion
of Its Range
Under the Act and our implementing
regulations, a species may warrant
listing if it is in danger of extinction or
likely to become so within the
foreseeable future throughout all or a
significant portion of its range. Having
determined that the Florida golden aster
is not in danger of extinction or likely
to become so within the foreseeable
future throughout all of its range, we
now consider whether it may be in
danger of extinction or likely to become
so within the foreseeable future in a
significant portion of its range—that is,
whether there is any portion of the
species’ range for which it is true that
both (1) the portion is significant, and
(2) the species is in danger of extinction
now or likely to become so within the
foreseeable future in that portion.
Depending on the case, it might be more
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efficient for us to address the
‘‘significance’’ question or the ‘‘status’’
question first. We can choose to address
either question first. Regardless of
which question we address first, if we
reach a negative answer with respect to
the first question that we address, we do
not need to evaluate the other question
for that portion of the species’ range.
For Florida golden aster, we chose to
evaluate the status question first. We
began by identifying portions of the
range where the biological status of the
species may be different from its
biological status elsewhere in its range.
For this purpose, we considered
information pertaining to the geographic
distribution of individuals of the
species, the threats that the species
faces, and the resiliency condition of
populations.
We evaluated the range of the Florida
golden aster to determine if the species
is in danger of extinction now or likely
to become so within the foreseeable
future in any portion of its range. The
range of a species can theoretically be
divided into portions in an infinite
number of ways. We focused our
analysis on portions of the species’
range that may meet the Act’s definition
of an endangered species or a threatened
species. For the Florida golden aster, we
considered whether the threats or their
effects on the species are greater in any
biologically meaningful portion of the
species’ range than in other portions
such that the species is in danger of
extinction now or likely to become so
within the foreseeable future in that
portion.
We examined the following threats:
development and climate change,
including cumulative effects. Currently,
there are 30 known extant Florida
golden aster populations occurring in
five counties (Hillsborough, Manatee,
Pinellas, Highlands, and Hardee
Counties), with 25 of these populations
occurring on conservation lands
(Federal, State, and conservation
easements). Climate change, as
discussed above, is uniformly acting
upon the species across its range, except
for sea level rise, which would only
potentially affect one population at Fort
De Soto County Park in Pinellas County.
As this would potentially impact just a
single population out of 30 populations,
we do not consider this concentration of
threats to be at a biologically meaningful
scale.
Although development is currently
concentrated in Pinellas County, that
activity would negatively impact in the
foreseeable future only five populations
that occur on private lands or along
roadways or railroad lines. However,
two of these populations have high and
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moderate resiliency (the remaining three
populations have low resiliency), and
this pattern will continue in the future.
The Pinellas County populations are
currently in low condition, and some
may become extirpated within the
foreseeable future due to development.
Therefore, our examination leads us to
find that there is substantial information
that the Pinellas County populations
may become in danger of extinction
within the foreseeable future.
We then proceeded to consider
whether this portion of the range (i.e.,
the Pinellas County populations) is
significant. For the purposes of this
analysis, the Service is considering
significant portions of the range by
applying any reasonable definition of
‘‘significant.’’ We assessed whether any
portions of the range may be
biologically meaningful in terms of the
resiliency, redundancy, or
representation of the entity being
evaluated. This approach is consistent
with the Act, our implementing
regulations, our policies, and case law.
Currently, the Pinellas County
populations represent a small portion
(less than 10 percent based on current
extant populations) of the species’
range, which is not a large geographic
area relative to the range of the species.
Further, these populations were all
introduced after listing (i.e., they are not
naturally occurring populations) and are
not contributing much to the viability of
the species. This portion does not
contribute high-quality habitat or
constitute high-value habitat for the
species. In addition, this portion does
not constitute an area of habitat that is
essential to a specific life-history
function for the species that is not found
in the remainder of the range. Therefore,
this area does not represent a significant
portion of the species’ range.
Accordingly, we find that the Florida
golden aster is not in danger of
extinction now or likely to become so
within the foreseeable future in any
significant portion of its range. This
does not conflict with the courts’
holdings in Desert Survivors v.
Department of the Interior, 321 F. Supp.
3d 1011, 1070–74 (N.D. Cal. 2018), and
Center for Biological Diversity v. Jewell,
248 F. Supp. 3d 946, 959 (D. Ariz. 2017)
because, in reaching this conclusion, we
did not apply the aspects of the Final
Policy on Interpretation of the Phrase
‘‘Significant Portion of Its Range’’ in the
Endangered Species Act’s Definitions of
‘‘Endangered Species’’ and ‘‘Threatened
Species’’ (79 FR 37578; July 1, 2014),
including the definition of ‘‘significant,’’
that those court decisions held to be
invalid.
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Determination of Status
Our review of the best available
scientific and commercial data available
indicates that the Florida golden aster
does not meet the definition of an
endangered species or a threatened
species in accordance with sections 3(6)
and 3(20) of the Act. In accordance with
our regulations at 50 CFR 424.11(e)(2)
currently in effect, Florida golden aster
does not meet the definition of an
endangered or threated species.
Therefore, we are removing the Florida
golden aster from the List of Endangered
and Threatened Plants.
Effects of This Final Rule
This final rule revises 50 CFR 17.12(h)
by removing the Florida golden aster
from the Federal List of Endangered and
Threatened Plants. On the effective date
of this rule (see DATES, above), the
prohibitions and conservation measures
provided by the Act, particularly
through sections 7 and 9, will no longer
apply to the Florida golden aster.
Federal agencies will no longer be
required to consult with the Service
under section 7 of the Act if activities
they authorize, fund, or carry out may
affect the Florida golden aster. There is
no critical habitat designated for this
species, so this rule does not affect 50
CFR 17.96.
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Post-Delisting Monitoring
Section 4(g)(1) of the Act requires us,
in cooperation with the States, to
implement a monitoring program for not
less than 5 years for all species that have
been recovered. Post-delisting
monitoring (PDM) refers to activities
undertaken to verify that a species
delisted due to recovery remains secure
from the risk of extinction after the
protections of the Act no longer apply.
The primary goal of PDM is to monitor
the species to ensure that its status does
not deteriorate, and if a decline is
detected, to take measures to halt the
decline so that proposing it as an
endangered or threatened species is not
again needed. If at any time during the
monitoring period, data indicate that
protective status under the Act should
be reinstated, we can initiate listing
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procedures, including, if appropriate,
emergency listing.
We have prepared a PDM plan for
Florida golden aster. The PDM plan: (1)
summarizes the status of Florida golden
aster at the time of proposed delisting;
(2) describes frequency and duration of
monitoring; (3) discusses monitoring
methods and potential sampling
regimes; (4) defines what potential
triggers will be evaluated to address the
need for additional monitoring; (5)
outlines reporting requirements and
procedures; (6) proposes a schedule for
implementing the PDM plan; and (7)
defines responsibilities.
We made the draft PDM plan
available for public comments with the
proposed rule published on June 24,
2021 (86 FR 33177). We did not receive
any comments on the draft PDM plan;
therefore, we are adopting the draft plan
as the final plan. The final PDM plan for
the species can be found at https://
www.regulations.gov under Docket No.
FWS–R4–ES–2019–0071. It is our intent
to work closely with our partners
towards maintaining the recovered
status of the Florida golden aster.
15779
remain sensitive to Indian culture, and
to make information available to Tribes.
We have determined that no Tribes will
be affected by this final rule because no
Tribal lands, sacred sites, or resources
will be affected by the removal of the
Florida golden aster from the List of
Endangered and Threatened Plants.
References Cited
A complete list of references cited is
available on the internet at https://
www.regulations.gov under Docket No.
FWS–R4–ES–2019–0071 and upon
request from the Florida Ecological
Services Field Office (see FOR FURTHER
INFORMATION CONTACT, above).
Authors
The primary authors of this final rule
are staff members of the Service’s
Species Assessment Team and the
Florida Ecological Services Field Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Plants, Reporting and
recordkeeping requirements,
Transportation, Wildlife.
Required Determinations
Regulation Promulgation
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 Secretary’s 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
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as set forth
below:
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PART 17—ENDANGERED AND
THREATENED WILDLIFE AND PLANTS
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 1531–
1544; and 4201–4245, unless otherwise
noted.
§ 17.12
[Amended]
2. In § 17.12, in paragraph (h), amend
the List of Endangered and Threatened
Plants by removing the entry for
‘‘Chrysopsis floridana’’ under
FLOWERING PLANTS.
■
Stephen Guertin,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. 2024–04278 Filed 3–4–24; 8:45 am]
BILLING CODE 4333–15–P
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Agencies
[Federal Register Volume 89, Number 44 (Tuesday, March 5, 2024)]
[Rules and Regulations]
[Pages 15763-15779]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-04278]
=======================================================================
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R4-ES-2019-0071; FF09E22000 FXES1113090FEDR 2223]
RIN 1018-BE00
Endangered and Threatened Wildlife and Plants; Removal of
Chrysopsis floridana (Florida Golden Aster) From the Federal List of
Endangered and Threatened Plants
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), are removing
the Florida golden aster (Chrysopsis floridana), a short-lived
perennial, from the Federal List of Endangered and Threatened Plants
(List) due to recovery. Our review indicates that the threats to the
species have been eliminated or reduced to the point that the species
has recovered and no longer meets the definition of an endangered or
threatened species under the Endangered Species Act of 1973, as amended
(Act). Accordingly, the prohibitions and conservation measures provided
by the Act will no longer apply to this species.
DATES: This rule is effective April 4, 2024.
ADDRESSES: This final rule, supporting documents used in preparing this
rule, the post-delisting monitoring plan, and the comments we received
on the June 24, 2021, proposed rule are available at https://www.regulations.gov under Docket No. FWS-R4-ES-2019-0071.
FOR FURTHER INFORMATION CONTACT: Lourdes Mena, Division Manager,
Florida Classification and Recovery, U.S. Fish and Wildlife Service,
Florida Ecological Services Field Office, 7915 Baymeadows Way,
Jacksonville, FL 32256; telephone 904-731-3336. Individuals in the
United States who are deaf, deafblind, hard of hearing, or have a
speech disability may dial 711 (TTY, TDD, or TeleBraille) to access
telecommunications relay services. Individuals outside the United
States should use the relay services offered within their country to
make international calls to the point-of contact in the United States.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. Under the Act, a species warrants
delisting if it no longer meets the definition of an endangered species
(in danger of extinction throughout all or a significant portion of its
range) or threatened species (likely to become an endangered species
within the foreseeable future throughout all or a significant portion
of its range). The Florida golden aster is listed as an endangered
species, and we are delisting it. Delisting a species can only be
completed by issuing a rule through the Administrative Procedure Act
rulemaking process (5 U.S.C. 551 et seq.).
What this document does. This rule removes the Florida golden aster
from the Federal List of Endangered and Threatened Plants based on the
species' recovery.
The basis for our action. Under the Act, we may determine that a
species is an endangered or threatened species because of 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. The determination to delist a species must be
based on an analysis of the same factors.
Under the Act, we must review the status of all listed species at
least once every 5 years. We must delist a species if we determine,
based on the best available scientific and commercial data, that the
species is neither an endangered species nor a threatened species. Our
regulations at 50 CFR 424.11(e) identify three reasons why we might
determine a species should be delisted: (1) The species is extinct, (2)
the species does not meet the Act's definition of an endangered species
or a threatened species, or (3) the listed entity does not meet the
Act's definition of a species. Here, we have determined that the
Florida golden aster does not meet the definition of an endangered
species or a threatened species; therefore, we are delisting it.
Previous Federal Actions
Please refer to the proposed delisting rule (86 FR 33177) for the
Florida golden aster published on June 24, 2021, for a detailed
description of previous Federal actions concerning this species.
Peer Review
A species status assessment (SSA) team prepared an SSA report for
the Florida golden aster. The SSA team was composed of Service
biologists, in consultation with other species experts.
[[Page 15764]]
The SSA report represents a compilation of the best scientific and
commercial data available concerning the status of the species,
including the impact of past, present, and future factors (both
negative and beneficial) affecting the species.
In accordance with our joint policy on peer review published in the
Federal Register on July 1, 1994 (59 FR 34270), and our August 22,
2016, memorandum updating and clarifying the role of peer review in
listing actions under the Act, we solicited independent scientific
review of the information contained in the Florida golden aster SSA
report. As discussed in the proposed rule, we sent the SSA report to
six independent peer reviewers and received two responses. The peer
reviews can be found at https://www.regulations.gov. In preparing the
proposed rule, we incorporated the results of these reviews, as
appropriate, into the SSA report, which was the foundation for the
proposed rule and this final rule. A summary for the peer review
comments and our responses can be found in the Summary of Comments and
Recommendations below.
Summary of Changes From the Proposed Rule
In this final rule, we make no substantive changes to our June 24,
2021, proposed rule. Minor, nonsubstantive changes have been made
throughout this final rule.
Summary of Comments and Recommendations
In the proposed rule published on June 24, 2021 (86 FR 33177), we
requested that all interested parties submit written comments on our
proposal to delist the Florida golden aster and the draft post-
delisting monitoring (PDM) plan by August 23, 2021. We also contacted
appropriate Federal and State agencies, scientific experts and
organizations, and other interested parties and invited them to comment
on the proposal. A newspaper notice inviting public comments was
published on June 30, 2021, in the Tampa Bay Times. We did not receive
any requests for a public hearing. All substantive information provided
during the comment period is addressed below.
Peer Reviewer Comments
As discussed in Peer Review above, we received comments from two
peer reviewers on the draft SSA report. The SSA report was also
submitted to our Federal, State, and Tribal partners for scientific
review. We received review from two partners. We reviewed all comments
we received from the peer and partner reviewers for substantive issues
and new information regarding the contents of the SSA report. The
reviewers did not raise any substantive issues and provided only
editorial comments that we incorporated into the final SSA report,
which was the foundation for the proposed rule and this final rule.
Public Comments
We reviewed all public comments for substantive issues and new
information regarding the species. Substantive comments we received
during the comment period are addressed below.
(1) Comment: Several commenters stated the species should not be
delisted because populations are performing poorly. Multiple commenters
pointed to the report titled, ``Demographic Data Collection to Assess
the Endangerment of Chrysopsis floridana 2020'' (Peterson et al. 2020,
entire) as supporting their position that the species should not be
delisted.
Our response: The report titled, ``Demographic Data Collection to
Assess the Endangerment of Chrysopsis floridana 2020'' (Peterson et al.
2020, entire) was funded by the Service to analyze a subset of known
populations and did not look at all known populations. The intent of
the effort was to collect data to provide additional information to
supplement the 2018 Florida golden aster SSA report. The results of
Peterson et al. (2020, entire) reinforce our determination that the
Florida golden aster no longer meets the Act's definition of an
endangered species or a threatened species.
The 18 sites for the report were chosen specifically based on aster
population size and habitat development risk, which results in
increased future management constraints. Eleven of the selected
populations were classified as low risk, and the remaining seven were
classified as high risk, based on modeling projections in the SSA
report (Service 2018, p. 35). Of the 18 populations analyzed for the
report, all populations were analyzed for demographic data, and 8 of
those also had stage class (i.e., seedlings, vegetative plants,
reproductive plants) data collected. Data were collected over a 3-year
period, and annual survival and annual seedling survival were
calculated each year. This approach was intended to provide an analysis
of the variation in populations across the species' range, looking at
population resiliency and habitat management effectiveness. The
analysis was a comparison of the populations' metrics between the
populations studied but is not comparable to the overall current
condition of the species. Stage structure was used as an indirect
measure of population health because fecundity data (seed production)
were not collected, and full demographic models could not be assembled
for the species.
Annual survival was variable among populations and across years.
Stage structure (``small vegetative'' plants, ``large vegetative''
plants, and ``reproductive'' plants) also varied over the 3-year
period, with demographically healthy populations having more seedlings
and the least healthy populations having more flowering plants. This
variation would be expected based on the annual variations in climate
conditions over time as well as the phenology of the species.
Demographic results indicated moderate annual survival rates for 2017-
2018 (75.6 percent) and 2018-2019 (71.8 percent). The annual survival
rate for the 2017-2018 populations ranged from 55-91 percent with
similar rates of 42-89 percent in 2018-2019. The annual seedling
survival (62.0 percent and 64.6 percent, respectively) was slightly
lower. The report concluded that at least 6 populations might be
considered healthy and self-sustaining, and it may be determined that
the other 12 populations (all on protected lands) will fare better in
future years given increased management efforts (ideally fire),
especially within wild populations.
Variation in survival rates could be attributed to the time since
the last fire, habitat management application, and/or age of the mature
plant during the study period. Florida golden aster is a short-lived
perennial (3-5 years) that flowers multiple years once reproductive.
Not knowing the age of the plants being analyzed over the short
timeframe in the randomly selected plots could have biased the results,
as some of the plants may have been already at the end of their
lifespan or not reproductive yet. In addition, consideration of early
versus late lifespan productivity or species cycles (phenology), which
are currently unknown, may be important factors influencing the
analyzed data. The survival rate for this species is described as
moderate; the annual survival rates for this aster are adequate for the
species and the habitat it occupies (Peterson et al. 2020, entire).
Although survival rates varied among introduced and wild populations
and varied based on the habitat management status of the population,
populations consistently showed seedling recruitment, which is an
indication of recruitment in all
[[Page 15765]]
populations regardless of health conditions.
Based on the most current survey across the species' range (2006-
2018), 30 known extant populations, natural and introduced, occur in
five counties. Of these, 25 populations occur on 22 protected and
managed conservation lands. The post-delisting monitoring plan will
utilize baseline data for the populations studied in the report to
further assess long-term trends.
(2) Comment: Some commenters stated the species should not be
delisted because recovery criteria for delisting have not been
achieved.
Our response: Recovery plans provide a roadmap for us and our
partners on methods of enhancing conservation and minimizing threats to
listed species, as well as measureable criteria against which to
evaluate progress towards recovery and assess the species' likely
future condition. However, they are not regulatory documents and do not
substitute for the determinations and promulgation of regulations under
section 4(a)(1) of the Act. A decision to delist a species is
ultimately based on an analysis of the best scientific and commercial
data available and consideration of the standards listed in 50 CFR
424.11(e) to determine whether a species is no longer an endangered
species or a threatened species, regardless of whether that information
differs from the recovery plan. According to the recovery plan there
are many paths for this species to be recovered without all the
criteria being fully met. The recovery plan states that one or more
criteria may be exceeded while other criteria may not yet be
accomplished. In this instance, we have determined that the threats to
Florida golden aster are minimized sufficiently and that the species no
longer meets the Act's definition of an endangered species or a
threatened species.
(3) Comment: One commenter indicated delisting was premature
because there was no data-driven management plan for the species. The
commenter further stated that while short-term monitoring has suggested
a role for fire in maintaining populations, critical data are lacking
pertaining to the best management practices to maintain Florida golden
aster habitat, specifically disturbance dynamics and the optimal fire
frequency for managing populations.
Our response: In our June 24, 2021, proposed rule (86 FR 33177), we
announced the availability of a draft PDM plan for the Florida golden
aster, and we requested comments on the draft PDM plan. We also
solicited comments on the draft PDM plan from agencies that manage
Florida golden aster on their conservation lands, as well as State and
county partners that have been engaged in the species' conservation. We
received comments from both the Florida Forest Service and Hillsborough
County's Environmental Lands Acquisition and Protection Program, and
their comments were incorporated into the final PDM plan. See Post-
delisting Monitoring, below, for more information.
The decision to revise the status of a species, or to delist a
species, is ultimately based on an analysis of the best scientific and
commercial data available to determine whether a species is no longer
an endangered species or a threatened species. Complete understanding
of specific data pertaining to best management practices for Florida
golden aster such as disturbance dynamics or the fire return intervals
for optimal survival and health, is not a requirement of the Act.
Nevertheless, the general response of Florida golden aster to
disturbance regimes is sufficiently understood to inform management.
The delisting of Florida golden aster should not discourage continued
research on the species and its habitat needs. Indeed, the PDM plan
includes recommendations for this type of research.
(4) Comment: One commenter noted that growing development
surrounding Florida golden aster populations will further complicate
fire management, which is important for maintaining suitable habitat.
It will become increasingly difficult for many areas where Florida
golden aster is present to be managed with fire, and there is little
evidence that mechanical disturbance could serve as an effective
surrogate for fire.
Our response: The development pressures on native landscapes
throughout peninsular Florida are challenging and will continue to
persist indefinitely. Habitat management on conservation lands in the
wildland-urban interface can experience various constraints. However,
not all conservation lands with Florida golden aster populations are
subject to these constraints, and development often does not preclude
fire management; for example, the national wildlife refuges in Florida
frequently conduct prescribed fires despite close proximity to
developed areas. Additionally, various treatments and techniques to
prepare fuel loads prior to prescribed fire application can also
overcome many of these constraints, along with managing the area
without the use of fire. New and innovative methods are constantly
being developed and employed to accomplish the desired habitat
conditions. Best management practices and sound management planning
alleviates many of the obstacles land managers encounter when pursing
optimal conditions in support of the targeted species.
While the commenter stated that mechanical disturbance is not as
effective as fire in maintaining habitat for the Florida golden aster,
mechanical treatments can be effective, if deployed correctly. We note
in the SSA report that in the absence of fire, habitat openness can be
maintained with mowing, hand removal of trees and shrubs near plants,
or other mechanical treatments. Populations have persisted along
periodically mowed rights-of-way (e.g., underneath powerlines, along
roads and railroads) for decades without a prescribed burn program
(Service 2018, p. 12).
(5) Comment: One commenter stated that keeping the species listed
will improve the Florida golden aster's chances of recovery, adding
that continued listing would provide support necessary to continue
research and conservation work for the species.
Our response: We agree that the protections of the Act have helped
recover the Florida golden aster, such that it no longer meets the
Act's definition of an endangered species or a threatened species.
Currently, the vast majority of the known populations occur on
protected and managed conservation lands and have at least moderate
resiliency. Additionally, we expect habitat management for the species
to continue, such that these populations will only increase, though
this was not relied on for the delisting determination. The Florida
golden aster, therefore, is recovered and no longer warrants the
protections of the Act, now or in the foreseeable future. Retaining the
species on the Federal List of Endangered and Threatened Plants would
be contrary to the direction of the Act and would continue to draw
resources from other species that still need the protections of the
Act.
Background
A thorough review of the taxonomy, life history, ecology, and
overall viability of the Florida golden aster is presented in the SSA
report available on https://www.regulations.gov under Docket No. FWS-
R4-ES-2019-0071. A summary of that information is presented here.
Florida golden aster is endemic to xeric (very dry) uplands east
and southeast of the Tampa Bay area of central Florida. The historical
range of
[[Page 15766]]
the Florida golden aster is thought to span parts of Hillsborough,
Manatee, Pinellas, Highlands, and Hardee Counties, but the true extent
of the historical range is uncertain because the ecosystems on which it
occurs were rapidly converted to residential, commercial, and
agricultural uses after European settlement of the region. Agriculture
began in 1880, with grazing and production of citrus and row crops.
Residential and commercial activity began around 1840, mainly in the
Tampa Bay area and beach communities through the 1940s and 1950s, but
suburban and rural areas started expanding in the 1960s and 1970s and
that expansion has continued at a consistent rate. The species was
first collected and described from a specimen in Manatee County in
early 1901, with subsequent collections in Pinellas and Hillsborough
Counties in the 1920s. The earliest known Manatee County and Pinellas
County populations occurred in coastal areas of Bradenton Beach and St.
Petersburg Beach. However, these populations have since been
extirpated. The last remaining natural population known to occur in
Pinellas County was discovered in 1983; however, a housing development
eliminated all available habitat by 1985.
When the species was listed as endangered in 1986 (see 51 FR 17974;
May 16, 1986), nine known extant populations of the species occurred in
five locations, all coastal, in southeastern Hillsborough County
(Wunderlin et al. 1981, entire). Since the listing of the species,
increased survey efforts have resulted in the discovery of additional
populations, including occurrences farther inland. Many of the newly
discovered locations have since been acquired as protected sites with
active conservation management activities implemented to improve
habitat conditions. As discussed below, introductions have occurred on
conservation lands in Hardee, Hillsborough, Manatee, and Pinellas
Counties. It is not known whether these introduction sites were
historically occupied by the Florida golden aster or, if so, how long
ago they supported natural populations.
Based on the most current surveys across the species' range (2006-
2018), 30 known extant populations, natural and introduced, occur in 5
counties (Hardee--4 populations, Highlands--1 population,
Hillsborough--16 populations, Manatee--5 populations, and Pinellas--4
populations; figure 1). Populations were delineated using a separation
distance of 2 kilometers (km) between occurrences (see Current
Condition, below, for more information). Of these, 25 populations occur
entirely or mostly on 22 protected sites; a protected site is a site
that has been acquired in fee simple and placed into long-term
conservation, or that has a conservation easement or other binding land
agreement by the site owner that shows a commitment to its conservation
in perpetuity. In addition, all protected sites have a management
agreement or plan both developed and implemented. None of the lands
occupied by the Florida golden aster are federally owned or managed but
rather they are owned and managed by a State, local, or nongovernmental
entity. The remaining five extant populations occur on private lands or
along roadways or railroad lines.
The most recent surveys (occurring between 2006 and 2018) show that
just over half of the Florida golden aster individuals occur in nine
introduced populations at eight sites. The earliest introductions, a
total of 10, were undertaken in 1986; three of those populations remain
extant in Hardee and Manatee Counties, while seven other introductions
in Pinellas and Hillsborough Counties failed. Introductions were again
initiated during 2008-2013, when Bok Tower Gardens introduced six
additional populations in Hardee, Manatee, and Pinellas Counties,
containing 24,825 plants (as of the most recent censuses, with about
12,000 in one population). Four of the six populations contain more
than 1,000 plants; the remaining two populations (North and South
Duette Preserve) are the most recently introduced populations (2013),
have been growing rapidly, and are surrounded by ample habitat and
little to no development, so they will also reach sizes comparable to
the other introduced populations.
According to the most recent surveys, approximately 50,000
individuals exist with more than 90 percent occurring in the 25
populations located on protected lands. Although this estimate is the
best available information, it gives only an approximation of the true
current abundance of the Florida golden aster because surveys are not
conducted every year and are conducted for different objectives.
Moreover, population sizes fluctuate annually. Twelve of the 30
populations had more than 1,000 individual plants present when last
observed. We note that a 56-km gap occurs between the easternmost
naturally occurring population in Manatee County and the nearest
naturally occurring population in Hardee County, and it is not
presently known whether this gap is due to the lack of suitable
habitat, lack of observation, a long-distance dispersal event, or
fragmentation of a formerly continuous distribution.
BILLING CODE 4333-15-P
[[Page 15767]]
[GRAPHIC] [TIFF OMITTED] TR05MR24.000
BILLING CODE 4333-15-C
Recovery Criteria
Section 4(f) of the Act directs us to develop and implement
recovery plans for the conservation and survival of endangered and
threatened species unless we determine that such a plan will not
promote the conservation of the species. Under section 4(f)(1)(B)(ii),
recovery plans must, to the maximum extent practicable, include
objective, measurable criteria which, when met, would result in a
determination, in accordance with the provisions of section 4 of the
Act, that the species be removed from listed status.
Recovery plans provide a roadmap for us and our partners on methods
of enhancing conservation and minimizing threats to listed species, as
well as measurable criteria against which to evaluate progress towards
recovery and assess the species' likely future condition. However, they
are not regulatory documents and do not substitute for the
determinations and promulgation of regulations required under section
4(a)(1) of the Act. A decision to revise the status of a species or to
delist a species is ultimately based on an analysis of the best
scientific and commercial data available to determine whether a species
is no longer an endangered species or a threatened species, regardless
of whether that information differs from the recovery plan.
There are many paths to accomplishing recovery of a species, and
recovery may be achieved without all the criteria in a recovery plan
being fully met. For example, one or more criteria may be exceeded
while other criteria may not yet be accomplished. In that instance, we
may determine that the threats are minimized sufficiently and that the
species is robust enough that it no longer meets the Act's definition
of an endangered species or a threatened species. In other cases, we
may discover new recovery opportunities after having finalized the
recovery plan. Parties seeking to conserve the species may use these
opportunities instead of methods identified in the recovery plan.
Likewise, we may learn new information about the species after we
finalize the recovery plan. The new information may change the extent
to which existing criteria are appropriate for identifying recovery of
the species. The recovery of a species is a dynamic process requiring
adaptive management that may, or may not, follow all the guidance
provided in a recovery plan.
We issued the recovery plan for the Florida golden aster on August
29, 1988. The primary objective of the recovery plan was to provide
sufficient habitat for the Florida golden aster, both through
protection of the sites and proper vegetation management. The recovery
plan calls for establishment of new populations of the species. The
recovery plan states that reclassification of this species to
threatened could be considered if 10 geographically distinct
populations are established in its three native counties, and delisting
could be
[[Page 15768]]
considered if 20 such populations are secured (USFWS 1988, p. 3).
Currently, Florida golden aster occurs in 30 geographically distinct
populations across five counties, 25 are on protected lands, and 18 of
these populations have high or very high resiliency (see table 2),
which is consistent with the recovery plan's delisting criterion.
Regulatory and Analytical Framework
Regulatory Framework
Section 4 of the Act (16 U.S.C. 1533) and the implementing
regulations in Title 50 of the Code of Federal Regulations set forth
the procedures for determining whether a species is an endangered
species or a threatened species, issuing protective regulations for
threatened species, and designating critical habitat for endangered and
threatened species. In 2019, jointly with the National Marine Fisheries
Service, the Service issued a final rule that revised the regulations
in 50 CFR part 424 regarding how we add, remove, and reclassify
endangered and threatened species and the criteria for designating
listed species' critical habitat (84 FR 45020; August 27, 2019). On the
same day, we issued a final rule that revised 50 CFR 17.31 and 17.71
(84 FR 44753; hereinafter, ``the 20194(d) rule'') and ended the
``blanket rule'' option for application of section 9 prohibitions to
species newly listed as threatened after the effective date ofthose
regulatory revisions (September 26, 2019). Blanket rules had extended
the majority of the protections (all of the prohibitions that apply to
endangered species under section 9 and additional exceptions to the
prohibitions) to threatened species, unless we issued an alternative
rule under section 4(d) of the Act for a particular species (i.e., a
species-specific 4(d) rule). The blanket rule protections continued to
apply to threatened species that were listed prior to September 26,
2019, without an associated species-specific rule. Under the 2019 4(d)
rule, the only way to apply protections to a species newly listed as
threatened is forus to issue a species-specific rule settingout the
protective regulations that are appropriate for that species. Our
analysis for this decision applied our current regulations, portions of
which were last revised in 2019. Given that we proposed further
revisions to these regulations on June 22, 2023 (88 FR 40742; 88 FR
40764), we have also undertaken an analysis of whether the decision
would be different if we were to apply those proposed revisions. We
concluded that the decision would have been the same if we had applied
the proposed 2023 regulations. The analyses under both the regulations
currently in effect and the regulations after incorporating the June
22, 2023, proposed revisions are included in our decision file.
The Act defines an endangered species as a species that is in
danger of extinction throughout all or a significant portion of its
range, and a threatened species as a species that is likely to become
an endangered species within the foreseeable future throughout all or a
significant portion of its range. The Act requires that we determine
whether any species is an endangered species or a threatened species
because of any of the following 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.
These factors represent broad categories of natural or human-caused
actions or conditions that could influence a species' continued
existence. In evaluating these actions and conditions, we look for
those that may have a negative effect on individuals of the species, as
well as other actions or conditions that may ameliorate any negative
effects or may have positive effects. The determination to delist a
species must be based on an analysis of the same five factors.
We use the term ``threat'' to refer in general to actions or
conditions that are known to or are reasonably likely to negatively
affect individuals of a species. The term ``threat'' includes actions
or conditions that have a direct impact on individuals (direct
impacts), as well as those that affect individuals through alteration
of their habitat or required resources (stressors). The term ``threat''
may encompass--either together or separately--the source of the action
or condition or the action or condition itself.
However, the mere identification of any threat(s) does not
necessarily mean that the species meets the statutory definition of an
endangered species or a threatened species. In determining whether a
species meets either definition, we must evaluate all identified
threats by considering the species' expected response and the effects
of the threats--considering those actions and conditions that will
ameliorate the threats--on an individual, population, and species
level. We evaluate each threat and its expected effects on the species,
then analyze the cumulative effect of all the threats on the species.
We also consider the cumulative effect of the threats considering those
actions and conditions that will have positive effects on the species,
such as any existing regulatory mechanisms or conservation efforts. The
Secretary determines whether the species meets the definition of an
endangered species or a threatened species only after conducting this
cumulative analysis and describing the expected effect on the species
now and in the foreseeable future.
The Act does not define the term ``foreseeable future,'' which
appears in the statutory definition of ``threatened species.'' Our
implementing regulations at 50 CFR 424.11(d) set forth a framework for
evaluating the foreseeable future on a case-by-case basis. The term
``foreseeable future'' extends only so far into the future as we can
reasonably determine that both the future threats and the species'
responses to those threats are likely. In other words, the foreseeable
future is the period of time in which we can make reliable predictions.
``Reliable'' does not mean ``certain''; it means sufficient to provide
a reasonable degree of confidence in the prediction. Thus, a prediction
is reliable if it is reasonable to depend on it when making decisions.
It is not always possible or necessary to define foreseeable future
as a particular number of years. Analysis of the foreseeable future
uses the best scientific and commercial data available and should
consider the timeframes applicable to the relevant threats and to the
species' likely responses to those threats in view of its life-history
characteristics. Data that are typically relevant to assessing the
species' biological response include species-specific factors such as
lifespan, reproductive rates or productivity, certain behaviors, and
other demographic factors.
Analytical Framework
The SSA report documents the results of our comprehensive
biological review of the best scientific and commercial data regarding
the status of the species, including an assessment of the potential
threats to the species. The SSA report does not represent our decision
on whether the species should be reclassified or delisted under the
Act. It does, however, provide the scientific basis that informs our
regulatory decisions, which involve the further application of
standards within the Act and its implementing regulations and policies.
[[Page 15769]]
To assess Florida golden aster viability, we used the three
conservation biology principles of resiliency, redundancy, and
representation (Shaffer and Stein 2000, pp. 306-310). Briefly,
resiliency is the ability of the species to withstand environmental and
demographic stochasticity (for example, wet or dry, warm or cold
years); redundancy is the ability of the species to withstand
catastrophic events (for example, droughts, large pollution events),
and representation is the ability of the species to adapt to both near-
term and long-term changes in its physical and biological environment
(for example, climate changes, pathogen). In general, species viability
will increase with increases in resiliency, redundancy, and
representation (Smith et al. 2018, p. 306). Using these principles, we
identified the species' ecological requirements for survival and
reproduction at the individual, population, and species levels, and
described the beneficial and risk factors influencing the species'
viability.
The SSA process can be categorized into three sequential stages.
During the first stage, we evaluated individual species' life-history
needs. The next stage involved an assessment of the historical and
current condition of the species' demographics and habitat
characteristics, including an explanation of how the species arrived at
its current condition. The final stage of the SSA involved making
predictions about the species' responses to positive and negative
environmental and anthropogenic influences. Throughout all these
stages, we used the best available information to characterize
viability as the ability of a species to sustain populations in the
wild over time. We use this information to inform our regulatory
decision.
The following is a summary of the key results and conclusions from
the SSA report; the full SSA report can be found at Docket No. FWS-R4-
ES-2019-0071 on https://www.regulations.gov.
Summary of Biological Status and Threats
In this discussion, we review the biological condition of the
species and its resources, and the threats that influence the species'
current and future condition, in order to assess the species' overall
viability and the risks to that viability.
Summary of SSA Analysis
For a species to be viable there must be adequate redundancy
(suitable number, distribution, and connectivity to allow the species
to withstand catastrophic events), representation (genetic and
environmental diversity to allow the species to adapt to changing
environmental conditions), and resiliency (ability of a species to
withstand unpredictable disturbance). Resiliency for Florida golden
aster improves with maintained open habitat. Lambert and Menges (1996,
pp. 121-137) recommend prescribed burning that mimics the historic burn
pattern (frequent low-intensity fires in sandhill, less frequent burns
in scrub, with fires primarily in late spring and summer) and periodic
mechanical disturbance of the ground cover during late winter or early
spring when seeds are dispersed. In the absence of fire, habitat
openness can be maintained with mowing, hand removal of trees and
shrubs near plants, or other mechanical treatments; populations have
persisted along periodically mowed rights-of-way (e.g., underneath
powerlines, along roads and railroads) for decades without a prescribed
burn program. Populations must be suitably large and connected to
provide a reservoir of individuals for cross-pollination, as plants
will not self-fertilize, and to maintain levels of genetic diversity
high enough to prevent harmful consequences from inbreeding depression
and genetic drift (Ellstrand and Elam 1993, pp. 217-242). Redundancy
improves with increasing numbers of populations, and connectivity
(either natural or human-facilitated) allows connected populations to
``rescue'' each other after catastrophes. Representation improves with
increased genetic diversity and/or environmental conditions within and
among populations.
Viability of the Florida golden aster has been and will continue to
be impacted both negatively and positively by anthropogenic and natural
influences. Historically, the primary threats to the Florida golden
aster were habitat loss (resulting from human development) and habitat
degradation due to lack of adequate habitat management. As threats to
habitat have been alleviated via habitat protection and management,
recovery has been further bolstered by captive propagation followed by
introduction into unoccupied sites.
Analysis of Threat Factors
Present or Threatened Destruction, Modification, or Curtailment of the
Species' Habitat or Range
The main threat to this species at the time of listing was the
destruction and modification of habitat. Habitat destruction,
modification, and degradation on private lands and habitat degradation
from lack of adequate habitat management on public lands remain the
primary risk factor to the species. The five populations occurring on
private lands remain subject to adverse human activity including
dumping, off-road recreational vehicles use, and land clearing.
However, these activities are no longer threats to the 25 populations
on protected conservation lands because of controlled access and
restricted use.
Lack of management, especially the absence of periodic fire,
historically led to habitat degradation throughout the species' range.
The Florida golden aster occurs in open, sandy patches that
historically were maintained by fire under natural conditions. Without
naturally ignited fires or prescribed fire applications, the habitat
becomes overgrown, resulting in unfavorable conditions for the species'
persistence. Ideal habitat management is generally regarded as
prescribed burning that mimics the historical burn patterns (frequent
low-intensity fires in sandhill, less frequent burns in scrub, with
fires primarily in late spring and summer) and periodic mechanical
disturbance of the ground cover during late winter or early spring when
seeds are dispersed (Lambert and Menges 1996, pp. 121-137). Initial
burning to restore the openness of degraded habitat involves frequent
intense fires, after which burning can be less intense and less
frequent to simply maintain the habitat. Failing to maintain open scrub
habitat can disrupt the Florida golden aster's reproduction, survival,
and dispersal (Lambert and Menges 1996, pp. 121-137).
As with habitat destruction and modification, this threat from lack
of management remains a concern mainly on private, non-conservation
lands. Populations that occur on conservation lands are often being
managed to maintain optimal open scrub habitat. However, budget
constraints, manageability, conflicting priorities, and other factors
(weather, lack of equipment, staff shortages, etc.) may preclude proper
management activities even on conservation lands. Additionally,
proximity to urbanized areas can limit the number of days available for
prescribed burns, and urbanization in the Tampa Bay area is increasing
rapidly (Xian et al. 2005, pp. 920-928). To be optimal, burn days must
have wind speeds and wind directions that do not unduly burden
urbanized areas with smoke. For this reason, large rural tracts of
habitat are easier to burn than small tracts tucked into developed
areas. Increasing commercial and residential development could lead to
further
[[Page 15770]]
decreases in the ability to conduct prescribed burning in the future,
which may or may not be replaced with adequate habitat management by
other means (e.g., mowing) that are more expensive than using fire. The
type of development also factors into management ability and
flexibility, with major roads, schools, hospitals, retirement homes
(places with vulnerable populations) weighing more heavily on the
decision of if/when to burn than other types of development (Camposano
2018, pers. comm.).
Since the time of listing, conservation efforts for the Florida
golden aster and other scrub habitat species have reduced the threat of
habitat destruction, modification, and degradation. These conservation
efforts include acquiring properties where the species naturally
occurs, introducing populations on conservation lands, and conducting
habitat management on conservation lands (e.g., prescribed burning).
While habitat destruction and modification may still occur on private
lands, 83 percent of the sites are on public conservation lands and,
therefore, for the most part, are adequately managed and protected.
Land acquisitions and introductions have increased the number of
established populations within the historical range and have resulted
in the expansion of the species' known range. Further, although the
species will be delisted under the Act on the effective date of this
rule (see DATES, above), the Florida golden aster will remain listed as
threatened under State laws. Based on the best available information,
we conclude that resources for necessary management activities on
conservation lands will continue.
Disease or Predation
At the time of listing, grazing by domestic livestock was
identified as a stressor because the species' populations were on
private lands and many of the properties were in cattle production.
However, at present, the 25 populations on conservation lands are not
subject to any agriculture practices. No cattle grazing occurs on any
of these properties. Therefore, we no longer consider grazing to be a
threat.
Inadequacy of Existing Regulatory Mechanisms
The Florida Administrative Code (FAC) chapter 5B-40 (Preservation
of Native Flora of Florida) provides the Florida Department of
Agriculture and Consumer Services limited authority to protect plants
on State and private lands (primarily from the standpoint of illegal
harvest). Florida golden aster is listed as an endangered plant under
this statute, which requires anyone wishing to willfully harvest,
collect, pick, remove, injure, or destroy any plant listed as
endangered growing on the private land of another, or on any public
land or water, to obtain the written permission of the owner of the
land or water or his legal representative (FAC 5B-40.003(1)(a)). A
permit is also required to transport for the purpose of sale, selling,
or offering for sale any plant contained on the State's endangered
plant list that is harvested from such person's own property (FAC 5B-
40.003(1)(c)). The delisting of the Florida golden aster under the Act
will not affect this State listing.
Several sites, consisting of thousands of plants, are now under
county and State protection. Specifically, Hillsborough County has
purchased considerable acreage through the Endangered Land Acquisition
and Protection Program (ELAPP) that contains several large populations
of Florida golden aster. In 1987, Hillsborough County passed the
Environmentally Sensitive Lands Ordinance that established the
foundation for ELAPP. This applies to nine populations on six sites in
Hillsborough County. In 1990, this ordinance was amended and approved
for another 20 years by increasing county taxes to allow additional
funds to acquire conservation lands. In November 2008, voters approved
the issuance of up to $200 million in bonds for additional purchases.
ELAPP has worked with the Southwest Florida Water Management
District and Florida Forever to jointly fund the acquisition of lands.
Some of this money is also used for ELAPP to actively manage their
properties to benefit Florida golden aster. Therefore, we find that the
existing regulatory mechanisms will provide sufficient protections to
the species and habitat after delisting, especially on public lands
with ordinance protection. Currently, 27 sites where the species occurs
are subject to Florida State law. These State and local protections
have proven effective. For example, prescribed burning will continue
through the ELAPP. Although we acknowledge that this could change in
the future, we do not anticipate any future changes to the
implementation of these programs at this time.
Other Natural or Manmade Factors Affecting the Species' Continued
Existence
Our analyses under the Act include consideration of ongoing and
projected changes in climate. The terms ``climate'' and ``climate
change'' are defined by the Intergovernmental Panel on Climate Change
(IPCC). A recent compilation of climate change and its effects is
available from reports of the IPCC (IPCC 2014, entire). 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 2007, p. 78). Various types of changes in climate can 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 the effects of
interactions of climate with other variables (e.g., habitat
fragmentation) (IPCC 2007, pp. 8-14, 18-19). In our analyses, we use
our expert judgment to weigh relevant information, including
uncertainty, in our consideration of various aspects of climate change.
The IPCC concluded that the climate system is warming (Pachauri et
al. 2014, entire). Effects associated with changes in climate have been
observed, including changes in arctic temperatures and ice, widespread
changes in precipitation amounts, ocean salinity, and wind patterns and
aspects of extreme weather including droughts, heavy precipitation,
heat waves, and the intensity of tropical cyclones (Pachauri et al.
2014, entire). Species that are dependent on specialized habitat types,
limited in distribution, or at the extreme periphery of their range may
be most susceptible to the impacts of climate change (Byers and Norris
2011, entire; Anacker et al. 2013, pp. 193-210). However, while
continued change is certain, the magnitude and rate of change is
unknown in many cases and could be affected by many factors (e.g.,
weather circulation patterns).
According to the IPCC, most plant species cannot naturally shift
their geographical ranges sufficiently fast to keep up with current and
high projected rates of climate change on most landscapes (IPCC 2014,
p. 13). Plant species with restricted ranges may experience population
declines as a result of the effects of climate change. The concept of
changing climate can be meaningfully assessed both by looking into the
future and reviewing past changes.
Using the National Climate Change Viewer and using greenhouse gas
emission scenario (representative concentration pathway (RCP) 8.5), we
calculated projected annual mean changes from 1981-2010 to those
projected for 2025-2049 for maximum
[[Page 15771]]
temperature, precipitation, soil storage, and evaporative deficit in
all counties where Florida golden aster occurs (Adler and Hostetler
2017, entire). We also calculated projected annual mean changes for a
more conservative greenhouse gas emission scenario (RCP 4.5) using the
same timeframes for maximum temperature, precipitation, soil storage,
and evaporative deficit in all counties where Florida golden aster
occurs (Adler and Hostetler 2017, entire). Based on these results, all
5 counties within the range of Florida golden aster will be subjected
to higher temperatures (annual mean increase of 2.6 degrees Fahrenheit
([deg]F) (RCP 4.5) or 2.9 [deg]F (RCP 8.5)) and slightly higher
precipitation (annual mean increase of 0.1 inch per month (RCP 4.5) or
0.2 inch per month (RCP 8.5)) in the period of 2025-2049 relative to
the period of 1981-2010.
Additionally, climate change will likely influence Florida golden
aster into the future by affecting habitat suitability and the ability
to manage habitat with prescribed fire. Species that are dependent on
specialized habitat types, limited in distribution (e.g., Florida
golden aster), or at the extreme periphery of their range may be most
susceptible to the impacts of climate change (Byers and Norris 2011,
entire; Anacker et al. 2013, pp. 193-210). There is evidence that some
terrestrial plant populations have been able to adapt and respond to
changing climatic conditions (Franks et al. 2014, pp. 123-139). Both
plastic (phenotypic change such as leaf size or phenology) and
evolutionary (shift in allelic frequencies) responses to changes in
climate have been detected. Given enough time, plants can alter their
ranges, resulting in range shifts, reductions, or increases (Kelly and
Goulden 2008, pp. 11823-11826; Loarie et al. 2008, p. 2502).
The climate in the southeastern United States has warmed about 2
[deg]F from a cool period in the 1960s and 1970s and is expected to
continue to rise (Carter et al. 2014, pp. 396-417). Projections for
future precipitation trends in the Southeast are less certain than
those for temperature, but suggest that overall annual precipitation
will decrease, and that tropical storms will occur less frequently, but
with more force (e.g., more category 4 and 5 hurricanes) than
historical averages (Carter et al. 2014, pp. 396-417). Climatic
changes, including sea level rise (SLR) and shifts in seasonal
precipitation, temperature, and storm cycles, are projected to impact
the southeastern United States over the next century. Under both lower
and higher emissions scenarios, temperatures are expected to increase
(Carter et al. 2018, pp. 751-752), and climate change is expected to
intensify the hydrologic cycle and increase the frequency and severity
of extreme events like drought and heavy rainfall (Carter et al. 2018,
p. 775). Increases in evaporation of moisture from soils and loss of
water by plants in response to warmer temperatures are expected to
contribute to increased frequency, duration, and intensity of droughts.
Local sea level rise impacts depend not only on how much the ocean
level itself is increasing, but also on land subsidence and/or changes
in offshore currents (Carter et al. 2014, pp. 396-417), and impacts on
terrestrial ecosystems can occur via submergence of habitat during
storm surges or permanently, saltwater intrusion into the water table,
and erosion. Of the current populations of the Florida golden aster,
only one (Fort De Soto County Park, Pinellas County) is directly
vulnerable to inundation from 0.3 m of sea level rise, a reasonable
estimate of sea level rise by 2050. Hotter and drier conditions in the
future could lead to fewer days with optimal conditions for prescribed
burning, which could lead to reduced habitat quality if land managers
are unable to make up for the lack of burning with adequate mechanical
treatment.
It is possible that there will be increases in the number of
lightning strikes and sizes and severities of resulting fires, which
could have a positive or negative effect on specific Florida golden
aster populations. Hurricanes similarly could have positive or negative
effects on the species. Prolonged flooding could harm populations, but
the mechanical disturbance of trees being uprooted from flood events
could improve habitat for colonizing species like the Florida golden
aster (Menges and Johnson 2017, pers. comm.).
Other potential climate change effects include changes in
temperature and precipitation. Projections for future precipitation
trends in the Southeast are less certain than those for temperature but
suggest that overall annual precipitation will decrease. Hotter and
drier conditions may complicate the ability to manage Florida golden
aster with prescribed fires. Some terrestrial plant populations have
been able to adapt and respond to changing climatic conditions (Franks
et al. 2014, entire). Both plastic (phenotypic change such as leaf size
or phenology) and evolutionary (shift in allelic frequencies) responses
to changes in climate have been detected. Both can occur rapidly and
often simultaneously (Franks et al. 2014, entire). However, relatively
few studies are available that (1) directly examine plant responses
over time, (2) clearly demonstrate adaptation or the causal climatic
driver of these responses, or (3) use quantitative methods to
distinguish plastic versus evolutionary responses (Franks et al. 2014,
entire).
As noted earlier, only one population (Fort De Soto County Park,
Pinellas County) is directly vulnerable to inundation from 0.3 meters
of sea level rise, a reasonable estimate of sea level rise by 2050.
Hotter and drier conditions in the future could lead to fewer days with
optimal conditions for prescribed burning, which could lead to reduced
habitat quality if land managers are unable to make up for the lack of
burning with adequate mechanical treatment. It is possible that there
will be increases in the number of lightning strikes and sizes and
severities of resulting wildfires, which could have a positive or
negative effect on specific Florida golden aster populations.
Hurricanes similarly could have positive or negative effects on the
species. Prolonged flooding could harm populations, but the mechanical
disturbance of trees being uprooted could improve habitat for
colonizing species like Florida golden aster (Menges and Johnson 2017,
pers. comm.). We have no additional information or data regarding
effects of climate change with respect to Florida golden aster
populations into the future; further research will be helpful to
determine how this species responds directly to changes in temperature
and water availability. However, from the known and forecasted
information, we anticipate that effects to Florida golden aster from
climate change will be limited and will not rise to the level of a
threat.
Other influences not discussed in detail here, either because they
are not thought to be a major threat or there is little information
available, include invasive plant species like cogongrass (Imperata
cylindrica), and future genetic consequences of small and/or
translocated populations.
Synergistic Effects
Many of the stressors discussed in this analysis could work in
concert with each other and result in a cumulative adverse effect to
Florida golden aster, e.g., one stressor may make the species more
vulnerable to other threats.
Synergistic interactions are possible between effects of climate
change and effects of other threats, such as mowing, dumping, off-road
recreational vehicle use, and land clearing. However, we currently do
not have information to determine the likely effects of climate
[[Page 15772]]
change on interaction/competition between species, or on drought
conditions. Uncertainty about how different plant species will respond
under a changing climate makes projecting possible synergistic effects
of climate change on Florida golden aster speculative. However, the
increases documented in the number of populations since the species was
listed do not indicate that cumulative effects of various activities
and stressors are affecting the viability of the species at this time.
Based on our analysis of future stressors, we do not anticipate that
cumulative effects will affect the viability of the species in the
foreseeable future. Likewise, climate change, as discussed above, with
hotter and drier conditions can add additional complexity to future
prescribed burns. Available habitat in those tracts that are easier to
burn, or that can be managed by other methods (e.g., mechanical
manipulation), will be sufficient. Similarly, most of the potential
stressors we identified either have not occurred to the extent
originally anticipated at the time of listing or are adequately managed
as described above. In addition, we do not anticipate significant
stressors to increase on publicly owned lands or lands that are managed
for the species.
Current Condition
Delineating Populations
For the SSA, we delineated populations using a 2-km separation
distance rule based on species expert opinion, resulting in 30
populations across five counties. This strategy differs from the 1-km
separation distance rule that was used in the most recent 5-year
review, which was based on NatureServe's default criteria for defining
plant populations (NatureServe 2004, entire). The team of species
experts providing input on the SSA suspected that 1 km is likely an
underestimate of the distance that gene flow can regularly occur via
pollination. While the exact insect pollinators of the Florida golden
aster are not known, studies on multiple bee species (major plant and
Chrysopsis pollinators) demonstrate foraging distances that regularly
exceed 1 km (Greenleaf et al. 2007, pp. 289-296; Hagler et al. 2011, p.
144).
Current Resiliency
Resiliency refers to the ability of populations to withstand
stochastic events, whether demographic, environmental, or
anthropogenic. Populations with low resiliency are highly vulnerable to
stochastic events and face a high risk of extirpation within the next
few decades. Populations with moderate resiliency are less likely to be
extirpated within the next few decades, but require additional growth
(with help of regular habitat management and/or restoration) to become
more self-sustaining and resilient to stochastic events. Populations
with high resiliency are unlikely to be extirpated within the next 30
years in the absence of catastrophes or significant declines in the
quality of habitat management. Populations with very high resiliency
are the most robust and resistant to stochastic fluctuations.
In the SSA, we assessed resiliency for each population using three
factors: (1) population size, (2) habitat protection, and (3) area of
available habitat. Other factors were considered that likely contribute
to population resiliency, but data were not available to assess them
over all or most of the populations including certain explicit measures
of habitat quality, fire management, existence of land management
plans, and population trends. While some past survey data are available
for many populations, species experts did not feel comfortable
comparing population counts across time periods. In many cases,
differences in population sizes were likely not a result of increasing
populations, but rather of differences in survey methodology, number of
surveyors, and/or areas searched (e.g., surveyors who were more likely
to visit known patches and not find new patches; alternately, a bias
toward larger counts over time as old patches are revisited and
additional patches are found). Nevertheless, we are confident that
these population data demonstrate resiliency of the species.
Regardless, this species has not been extensively studied; therefore,
there was some uncertainty in the SSA in precisely how these factors
influenced Florida golden aster population resiliency.
Population Size
Population size is both a direct contributor to resiliency and an
indirect indicator of resiliency. Small populations are more
susceptible to demographic and environmental stochastic events than
larger populations. Small populations are also more likely to suffer
from decreased fitness because of low genetic diversity from inbreeding
or genetic drift (Willi et al. 2005, pp. 2255-2265). For Florida golden
aster, large populations are more buffered from the effects of
prescribed burning or other disturbances, which are necessary to
maintain open habitat but can temporarily reduce population sizes by
killing plants. Indirectly, large population sizes are likely
indicative of other conditions that contribute to population
resiliency. For example, in the SSA, we did not have adequate data to
assess habitat quality and the quality of management at all the Florida
golden aster populations; therefore, we assumed large population sizes
likely generally reflect good habitat quality and management (among
other factors) compared to smaller populations, although this
assumption may not hold in all cases.
We categorized populations into 4 size classes: fewer than 100
individuals, 100-500 individuals, 501-1,000 individuals, and more than
1,000 individuals. Each population size class was associated with one
of the following baseline resiliency classes, respectively: low,
moderate, high, and very high (explained further below).
We chose the population size threshold between high and very high
resiliency of 1,000 individuals because it is the typical population
size used to rank element occurrences as having ``excellent viability''
and likely to persist for the next 20-30 years (NatureServe 2008,
entire). This is a generic population size limit that was not
specifically tailored to Florida golden aster with empirical data.
Further support for using 1,000 individuals as the threshold for the
highest resiliency category came from a study of 10-year extirpation
rates for populations of varying sizes of eight short-lived plant
species in Germany (Matthies et al. 2004, pp. 481-488). In this study,
for seven of eight species, the probability of population persistence
increased with population size, and all populations of more than 1,000
individuals (flowering plants) persisted for the duration of the 10-
year study.
We obtained the most recent size data for all 30 populations, with
data collected as recently as 2018 for some populations, and none older
than 2006 for any population. However, population sizes have
undoubtedly changed since the most recent surveys, as populations
fluctuate in response to management actions, time since management,
environmental events, stochastic demographic processes, and so forth.
Thus, the reported numbers reflect best available estimates for
population sizes, rather than precise counts meant to represent actual
current population sizes. According to the SSA report, population sizes
include all plants counted, whether flowering or not. Survey data for
some populations provide separate counts for each life stage, but for
many populations, survey data are simply numbers with no information
about whether that number
[[Page 15773]]
was only flowering plants, or all plants (Service 2018, p. 22). Using
total plant numbers, and assuming that ambiguous counts are minimum
counts of total plants in each population, we were conservative in our
population counts. The alternative of assuming that ambiguous counts
are of only flowering adult plants, when they may include basal
rosettes, would inflate population sizes in cases where the assumption
was wrong.
Habitat Protection
Habitat was considered ``protected'' if it was acquired in fee
simple and placed into long-term conservation by a nongovernmental,
local, State, or Federal entity, or if there is a binding land
agreement. Protected sites have management plans developed and being
implemented. The effect of the degree of habitat protection on
resiliency is discussed below.
Habitat Area Available
Florida golden aster population sizes fluctuate and can occur in
high densities in small patches of habitat. However, as a general rule
of thumb for a given population size, a population covering a large
area will be more resilient than a population covering a small area. A
perturbation of the same size will have a proportionally larger effect
on small-area populations than large-area populations. In assessing
population resiliency, we considered the amount of habitat available
rather than the amount of habitat occupied for two reasons. First, the
amount of area occupied was very uncertain for most populations.
Surveys are likely to return to known patches of the Florida golden
aster, but new patches can be easily missed, and it is likely that the
data we have underestimates the true amount of area occupied by the
Florida golden aster. Adding to the uncertainty, the most current
spatial data for some populations comes from 2006, and may no longer
reflect the current distribution at those sites. Second, population
footprints are not always static across available habitat; the Florida
golden aster can spread into unoccupied areas as populations grow, or
shift across a landscape as different areas become more or less
suitable or both. For this reason, we used the amount of habitat
available for populations to occupy currently, grow into, or shift into
as a factor contributing to population resiliency. We identified
available habitat within a 2-km radius around known occurrences,
consistent with the assumption we made about pollinator movement when
delineating populations. We characterize the available habitat for
populations as small or large, with 14.2 hectares as the threshold
between the two groups. This value was selected based on natural breaks
in the data and expert input.
Classifying Resiliency Based on the Selected Factors
Resiliency classes were based primarily on population size as
described above, with four resiliency classes corresponding to four
population size categories. Populations with fewer than 100 individuals
were determined to have low resiliency. Within the three higher
population size categories (100-500, 501-1,000, and more than 1,000
plants), populations were assigned a baseline resiliency score
associated with their population size (moderate, high, or very high,
respectively). This baseline score could then be lowered by either of
the two other factors, habitat protection and habitat area available;
see table 1 below.
Table 1--Strategy for Assigning Current Resiliency Scores to Populations of C. floridana
----------------------------------------------------------------------------------------------------------------
Population size (# plants) Habitat protected Habitat not protected Habitat area available
----------------------------------------------------------------------------------------------------------------
<100................................ Low Small.
Large.
--------------------------------------------------
100-500............................. Low.................... Low.................... Small.
Moderate............... Low.................... Large.
501-1,000........................... Moderate............... Moderate............... Small.
High................... Moderate............... Large.
>1,000.............................. High................... High................... Small.
Very High.............. High................... Large.
----------------------------------------------------------------------------------------------------------------
Populations that occur on non-protected lands were assigned to the
resiliency class one step lower than they would if they were on
protected lands. By doing this, we did not intend to discount the
importance of populations on non-protected lands to the viability of
the species or imply that owners of these parcels are managing the land
poorly or are harming the Florida golden aster. Large populations of
Florida golden aster can be supported on private lands. For example,
when private landowners burn pasture to improve forage for cattle, they
may improve habitat for Florida golden aster. However, even large
populations of fire-adapted scrub plants can rapidly decline due to
poor management (e.g., Polygal lewtonii, Weekley and Menges 2012,
entire; Warea carteri, Quintana-Ascenscio et al. 2011, entire), and
private lands that are not protected for conservation are at higher
risk of changes in management or land use that could harm Florida
golden aster populations. For populations that extend across property
boundaries and contain individuals occurring on both protected and non-
protected lands, we used the protection status that applied to most
individuals to classify the entire population.
Populations occupying or surrounded by a small area of available
habitat were assigned to the resiliency class one step lower than they
would otherwise be assigned if they existed within a larger area of
available habitat, as they are less able to withstand and recover from
perturbations or shift across a landscape as habitat quality changes.
For any populations experiencing both resiliency-reducing conditions
(small habitat area on non-protected lands), the resiliency score was
only reduced one step rather than being reduced twice (i.e., once for
each condition). The Duette populations were the most recently
introduced populations. They have been growing rapidly and are
surrounded by ample habitat and little to no development; therefore,
these two populations were projected to increase from high to very high
resiliency.
Summaries of the 30 delineated populations and their resiliency
scores can be found in the SSA report (Service 2018, p. 32) and in
table 2, below. In conclusion, resiliency scores remained stable.
[[Page 15774]]
Table 2--Summary of Current Resiliency Scores by Protected Status for Florida Golden Aster
----------------------------------------------------------------------------------------------------------------
Resiliency class All populations Protected Not protected
----------------------------------------------------------------------------------------------------------------
Very High................................................. 7 7 0
High...................................................... 11 10 1
Moderate.................................................. 6 5 1
Low....................................................... 6 3 3
----------------------------------------------------------------------------------------------------------------
Current Redundancy and Representation
Redundancy for Florida golden aster is naturally low because it is
an endemic species with a narrow range in Florida around the Tampa Bay
region and Hardee County farther inland (with one population just
across the border in Highlands County). The entire species' range spans
five counties, with half of the populations occurring in Hillsborough
County (see figure 2, below). The longest distance between two
populations is 131 km. However, as this is a narrow-ranging endemic,
the spatial distribution of populations across its range does confer a
moderate amount of redundancy, defined as the ability of the species to
withstand catastrophic events. Catastrophic events could include, among
others, fires occurring too frequently, droughts, disease outbreaks, or
hurricanes with prolonged flooding, each of which have impacts at a
different spatial scale. No information is known about seedbank
resiliency in the soil for this species; without knowing this, it is
difficult to predict long-term impacts of catastrophes.
The 30 known populations are distributed in three main groupings.
There are about 20-30 km between each of the groupings, providing a
buffer around each that may protect them from catastrophic events
affecting the others (e.g., disease outbreak, depending on transmission
type and vectors). Within each geographic cluster, there are at least
two highly or very highly resilient populations, which could serve as
sources to naturally recolonize populations lost to catastrophic
events. The Hardee-Highlands cluster has the lowest redundancy (two
moderately resilient populations, six populations total) and is the
most isolated from the other clusters. The Pinellas cluster has the
next lowest redundancy of resilient populations (3 highly resilient
populations, 4 populations total), and the Hillsborough-Manatee cluster
has the highest redundancy (13 resilient populations, 20 populations
total); see figure 2 below. Another factor contributing to redundancy
is the wide range of property ownership; with so many managing
entities, the species is buffered against poor management of any one
entity (e.g., due to budget issues or changing priorities). Based on
the spatial distribution of resilient populations managed by a variety
of entities across a narrow range, current redundancy is considered
qualitatively to be low to moderate. Rather than solely relying on this
rather subjective classification in assessing the current viability of
the species, characterizing current redundancy is most useful in
comparison to redundancy under the future scenarios; see Future
Conditions discussion below.
[GRAPHIC] [TIFF OMITTED] TR05MR24.001
[[Page 15775]]
Representative units for this species could not be defined based on
available data, with representation defined as the ability of the
species to adapt to changing environmental conditions. Species experts
contributing to the SSA suspect that there might be representative
units with different genetic adaptations associated with soil
differences, elevation above the water table, fire regime, or habitat
structure. However, there are no data currently to confirm or refute
these hypotheses. Genetic studies have found little to no genetic
clustering among populations, with 80 percent of observed genetic
variation occurring within populations, and only 20 percent of the
variation attributable to between-population differences (Markham 1998,
p. 41). These results support the existence of a single representative
unit for the species. However, that study did not examine genetic
markers known to be associated with adaptive traits. Vital rates and
morphology were observed to differ between individuals from different
source populations that were grown at Bok Tower Gardens and introduced
to other sites (Campbell 2008, entire). This observation provides
evidence that there might be adaptive differences between different
``types'' of the Florida golden aster across the species' range.
However, without any firm evidence to define representative units, we
refrain from doing so here. Future research on the Florida golden
aster's genetics, life history, and habitat differences can provide a
more definitive basis for defining representative units in future
iterations of the SSA report.
Future Conditions
Analytical Framework
For the SSA report, we developed three plausible future scenarios
under which to capture the breadth of all likely future variability and
assess the future viability of Florida golden aster in terms of
resiliency, redundancy, and representation. Based on expert opinion,
the lifespan of the Florida golden aster, ideal fire-return intervals
(at least every 10 years), uncertainty about future conditions, and
lack of knowledge about certain aspects of Florida golden aster
ecology, we chose to project populations 20 years into the future under
each scenario, although some of these projections could be reasonably
expected to continue for some time after the 20 years. With
approximately 30 years of real data and trends, we project that the
same trends will continue. The three hypothetical future scenarios are
Status Quo, Pessimistic, and Targeted Conservation.
In considering development as a threat, we used the SLEUTH (Slope,
Land use, Excluded, Urban, Transportation and Hillshade; Jantz et al.
2010, p. 34:1-16) data sets from the years 2020 (closest to current
year) and 2040 (closest to 20 years in the future), and examined the
area predicted, with at least 80 percent probability, to be urbanized.
Therefore, our assessment was both quantitative, calculating the area
within the 5-km buffer surrounding each population that was urbanized
at each time point, and qualitative, inspecting the distribution of
urbanization and major roads within that area (e.g., is the
urbanization concentrated to one side of the population or surrounding
it).
With both the quantitative and qualitative assessments, we
categorized populations as having either low risk or high risk of
development impacting management for Florida golden aster. We defined
high risk of impacting management as greater than 50 percent chance of
negatively impacting management, and less than 50 percent for low risk.
Populations classified as having low risk from development averaged 7.9
percent developed area within the 5-km buffer by 2040, with a range of
0 to 39 percent developed. Populations classified as having high risk
from development averaged 45.5 percent developed area within the same
buffer, ranging from 23 to 85 percent. For three populations with a
percent of developed area in the overlapping range between the two
categories (23 to 39 percent developed), the deciding factor between
low risk and high risk was the distribution of development and roads
around the population.
Habitat Quantity
Habitat quantity can be negatively impacted by development or land
use change (particularly on private lands) or positively impacted by
land acquisition, restoration, and introductions into unoccupied sites
that already have presumably suitable habitat.
Habitat Quality
Habitat quality is closely tied to active habitat management to
maintain openness either by prescribed burning or by other types of
management. In constructing our scenarios, we considered two avenues by
which future habitat management can be influenced: (1) the level of
habitat management effort and (2) the amount and type of development
near the Florida golden aster populations (to the extent the
development affects the ability to conduct management actions, such as
prescribed burns). First, the managing entities can choose their
desired level of management effort by implementing (or not) a
management plan or by allocating funding or personnel to or away from
habitat management among competing priorities and limited resources.
For our scenarios, we allowed for three levels of habitat management
effort by managing entities. The first was management for stability, a
moderate level of management that would be expected to maintain
populations at their current size. The other two management levels were
an increase, or a decrease, compared to management for stability. An
increase in management effort would be expected to grow populations,
while a decrease in management would be expected to result in
population declines.
The second avenue by which future habitat management can be
influenced is development, particularly major roads and types of
development associated with ``vulnerable'' human populations (e.g.,
schools, hospitals). This kind of development surrounding habitat
limits management via prescribed burns by limiting the days that burns
can take place--weather conditions must align to ensure proper smoke
management. For example, if a population is surrounded by nearby
development to the north and west, it can only be burned when the wind
is blowing to the south and east. As more development surrounds
populations, there is less flexibility for prescribed burns. However,
the appropriate radius around populations within which development
might impact management ranges from 0.8 km up to 8.0 km as the
appropriate radius depends on a variety of factors for each burn,
including the type of development, temperature, humidity, wind
conditions, size of the planned burn, risk tolerance of those
implementing the burn, and other factors. For the SSA, we chose an
intermediate value, 5 km, in which to examine current and predicted
future development. In choosing this concrete value, we acknowledged
that this number is quite variable, and some burns will need to
consider areas greater or less than 5 km away, but this value allowed
us to gain a general understanding of the risks of development on
managing surrounding populations.
Within a 5-km radius around the Florida golden aster occurrences,
we used geographic information systems (GIS) to examine current and
projected urbanization and roads. Urbanization data came from the
SLEUTH model, and road data were available from the
[[Page 15776]]
Florida Department of Transportation. The SLEUTH model has previously
been used to predict probabilities of urbanization across the
southeastern United States in 10-year increments, and the resulting GIS
data are freely available (Belyea and Terrando 2013, entire). For our
20-year future projection, we used the SLEUTH data sets from the years
2020 and 2040, and examined the area predicted, with at least 80
percent probability, to be urbanized. Our assessment was both
quantitative, calculating the area within the 5-km buffer surrounding
each population that was urbanized at each time point, and qualitative,
inspecting the distribution of urbanization and major roads within that
area (e.g., is the urbanization concentrated to one side of the
population or surrounding it?). With this quantitative and qualitative
assessment, we categorized populations as having either a low risk or a
high risk of development impacting the ability to manage the
population.
These two aspects of future management, (1) management resources
and willingness of the entity to manage, and (2) impacts of surrounding
development on management, interacted in our future scenarios in the
following way: with decreases in management effort (compared to
management for stable populations), population resiliency decreased one
level. With management for stability, population resiliency stayed the
same as the current condition resiliency when there was low risk of
development impacts; but where there was a high risk, resiliency
decreased one level, reflecting that management will be more
challenging with higher risk from development. With increases in
management effort, population resiliency increased when there was low
risk of development impacts, but stayed the same when there was a high
risk; the increased management effort canceled out the increased risk
caused by development.
Future Scenarios
Status Quo
Under the Status Quo scenario, no new protected areas were acquired
and no new populations were introduced. Management efforts for all
populations were maintained at current levels, assuming that the
ability to manage would not be hampered climate change or other
factors. This scenario also assumes that conservation commitments
outlined in management plans currently being implemented will continue.
Of the introductions since 2008, all have more than 1,000 plants except
for the two populations at Duette Preserve (North and South).
Pessimistic
Under the Pessimistic scenario, management effort on all
populations decreased, resulting in a drop in resiliency scores across
the board. Additionally, based on uncertainty in whether populations on
non-protected lands would continue to be managed in a way that is
compatible with continued Florida golden aster persistence, in this
scenario all populations on non-protected lands were assumed to be lost
due to presumed land use or management change. As with the Status Quo
scenario, no new protected areas were acquired, and no new populations
were introduced.
Targeted Conservation
Under the Targeted Conservation scenario, populations with high and
very high resiliency were managed to maintain their rank. In cases
where populations had a high risk of development limiting the ability
to manage, this goal involved an increase in management effort compared
to what would be needed to maintain the same level of resiliency for a
population with a low risk of development impacts. Populations with
currently moderate resiliency on protected lands received management
effort increases to either move them into the high resiliency class
(low risk from development) or maintain moderate resiliency (high risk
from development). Conservation resources were steered towards
maintaining and growing these larger populations, and not as much
towards rescuing populations that currently have low resiliency.
Additionally, five new sites were selected across the species' range in
which to introduce new populations, thus improving species redundancy.
Likelihood of Scenarios
Of these three scenarios, the Status Quo scenario is the most
likely to occur, although the Targeted Conservation scenario represents
a likely future if both habitat-focused management (prescribed burning
and mechanical or manual habitat management) by a variety of partners/
managing entities and species-specific conservation (captive
propagation and introductions) are prioritized and well-funded. The
Pessimistic scenario was unlikely; given that Florida golden aster
populations span so many different ownerships, it is unlikely that all
the different managing entities will develop the land especially when
there are other co-occurring endangered, threatened, and candidate
species occupying the same habitat (e.g., Florida scrub-jay, Aphelocoma
coerulescens; eastern indigo snake, Drymarchon couperi;. The Targeted
Conservation scenario was not likely with current conservation
resources but, as noted above, could reflect a likely future if the
needed management and conservation actions are prioritized and well-
funded.
Future Resiliency
Future (20 years) resiliency of Florida golden aster populations
under three scenarios is summarized in the SSA report (Service 2018, p.
49), and is presented below in table 3. As implied by the scenario
name, resiliency of populations under the Pessimistic scenario was
predicted to be poor, with only 7 highly resilient populations, a
decrease from 18 currently highly or very highly resilient populations.
Under the Status Quo scenario, we expect resiliency to drop to 12
highly or very highly resilient populations due solely to the effect of
development limiting the ability to adequately manage habitat. Under
the Targeted Management scenario, focused management and conservation
efforts to counteract detrimental effects of urbanization, the growth
of existing populations, and the introduction of new populations are
expected to result in significant gains in resilient populations, with
an increase from 18 to 27 highly or very highly resilient populations
expected highly or very highly resilient populations.
[[Page 15777]]
Table 3--Summary of Resiliency Scores Tallied Across All Populations of Florida Golden Aster for the Current
Condition and Future Condition Under Three Hypothetical Scenarios: Status Quo, Pessimistic, and Targeted
Conservation
----------------------------------------------------------------------------------------------------------------
Targeted
Resiliency class Current Status quo Pessimistic conservation
----------------------------------------------------------------------------------------------------------------
Very High....................................... 7 4 0 9
High............................................ 11 8 7 18
Moderate........................................ 6 11 11 2
Low............................................. 6 3 5 2
Likely Extirpated............................... 0 4 7 4
----------------------------------------------------------------------------------------------------------------
Future Redundancy and Representation
Redundancy 20 years in the future was expected to decrease compared
to current condition under the Status Quo and Pessimistic Scenarios. In
all scenarios, the majority of highly and very highly resilient
populations were found in Hillsborough and Manatee Counties. All
redundancy of highly resilient populations in Pinellas County and the
Hardee and Highlands Counties cluster is lost under the Pessimistic
scenario. In the Status Quo scenario, where drops in resiliency were
due to development risks to management, no highly resilient populations
remained in the heavily urbanized Pinellas County. Even in the Targeted
Conservation scenario, redundancy within Pinellas County did not
improve, but both the number and distribution of highly resilient
populations in the other two clusters did improve. We did not assess
representation in the future due to a present lack of information
needed to delineate representative units.
We note that, by using the SSA framework to guide our analysis of
the scientific information documented in the SSA report, we have
analyzed the cumulative effects of identified threats and conservation
actions on the species. To assess the current and future condition of
the species, we evaluate the effects of all the relevant factors that
may be influencing the species, including threats and conservation
efforts. Because the SSA framework considers not just the presence of
the factors, but to what degree they collectively influence risk to the
entire species, our assessment integrates the cumulative effects of the
factors and replaces a standalone cumulative-effects analysis.
Conservation Efforts and Regulatory Mechanisms
The Florida Administrative Code 5B-40 (Preservation of Native Flora
of Florida) provides the Florida Department of Agriculture and Consumer
Services (FDACS) limited authority to protect plants on State and
private lands (primarily from the standpoint of illegal harvest).
Florida golden aster is listed as an Endangered Plant under this
statute, which requires anyone wishing to ``willfully harvest, collect,
pick, remove, injure, or destroy any plant listed as endangered growing
on the private land of another or on any public land or water'' to
``obtain the written permission of the owner of the land or water or
his legal representative'' (FAC 5B-40.003(1)(a)). A permit is also
required to transport ``for the purpose of sale, selling, or offering
for sale any plant contained on the endangered plant list which is
harvested from such person's own property'' (FAC 5B-40.003(1)(c)).
There are now several sites and thousands of plants under county
and State protection. Specifically, Hillsborough County has purchased
considerable acreage through the Endangered Land Acquisition and
Protection Program that contain several large populations. Golden aster
is also documented at Lake Manatee State Recreation Area and Little
Manatee River State Park in Manatee and Hillsborough Counties.
Currently, 27 sites where the species occurs are subject to State laws.
Determination of Florida Golden Aster's Status
Section 4 of the Act (16 U.S.C. 1533) and its implementing
regulations (50 CFR part 424) set forth the procedures for determining
whether a species meets the definition of an endangered species or a
threatened species. The Act defines an endangered species as a species
that is in danger of extinction throughout all or a significant portion
of its range, and a threatened species as a species that is likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range. The Act requires that we
determine whether a species meets the definition of an endangered
species or a threatened species because of any of the following
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.
Status Throughout All of Its Range
After evaluating threats to the species and assessing the
cumulative effect of the threats under the Act's section 4(a)(1)
factors, we find that the present or threatened destruction,
modification, or curtailment of Florida golden aster habitat (Factor
A), which was the basis for listing the species, is no longer a threat.
At the time of listing, Florida golden aster was thought to persist
only in Hillsborough County. Now, the species is known to occur in four
additional counties: Hardee, Highlands, Mantee, and Pinellas Counties.
While destruction and modification of habitat is still the primary
threat to the species, the magnitude of this threat has been greatly
reduced since listing. Further, the number of populations has
increased. Under the recovery plan for the species, delisting could be
considered if 20 populations were secured. The number of known extant
populations has increased from 9 in 1986 to 30 in 2017 because of
additional surveys, habitat restoration, and outplanting within the
historical range of the species. Of those 30 populations, 25
populations are located on protected conservation lands, and 22 of
those 25 populations have been determined to have at least moderate
resiliency. We expect current levels of management to continue these
conservation lands at these locations, and we anticipate the number of
individuals within the populations to increase.
For the determination of whether the species is likely be become
endangered within the foreseeable future throughout all its range, and
thus meet the Act's definition of a threatened species, we considered
the ``foreseeable future'' to be 20 years into the future under the
three hypothetical future scenarios. Our SLEUTH tool projected future
possible development to 20 years, NatureServ
[[Page 15778]]
considers large population sizes likely to persist over the next 20-30
years, and considerations of climate change make projections beyond 20
to 30 years much more speculative. Also, given the average lifespan of
the species (approximately 3-5 years), a period of 20 to 30 years
allows for multiple generations and detection of any population
changes. Under all three scenarios evaluated, the Florida golden aster
is expected to continue to persist across its currently known range.
Under the Status Quo scenario, which is also the most likely to occur,
12 populations are projected to be highly or very highly resiliency and
11 moderately resilient across all three geographic clusters, as
habitat modification is no longer a threat for the populations on
protected lands and current management of those lands is expected to
continue. Four populations (three natural and one introduced) currently
in low condition are projected to become extirpated in the Status Quo
scenario. Even under the Pessimistic scenario, which is least likely to
occur, 7 populations are projected to be in high condition and 11 in
moderate condition, all of which occur on protected lands with
conservation management expected to continue at some level. Given that
most populations projected to remain extant with at least moderate
resiliency are on protected lands managed for scrub habitat, it is
unlikely the species will become endangered within the foreseeable
future throughout all its range. Thus, after assessing the best
available information, we conclude that the Florida golden aster is not
in danger of extinction now or likely to become so within the
foreseeable future throughout all its range.
Status Throughout a Significant Portion of Its Range
Under the Act and our implementing regulations, a species may
warrant listing if it is in danger of extinction or likely to become so
within the foreseeable future throughout all or a significant portion
of its range. Having determined that the Florida golden aster is not in
danger of extinction or likely to become so within the foreseeable
future throughout all of its range, we now consider whether it may be
in danger of extinction or likely to become so within the foreseeable
future in a significant portion of its range--that is, whether there is
any portion of the species' range for which it is true that both (1)
the portion is significant, and (2) the species is in danger of
extinction now or likely to become so within the foreseeable future in
that portion. Depending on the case, it might be more efficient for us
to address the ``significance'' question or the ``status'' question
first. We can choose to address either question first. Regardless of
which question we address first, if we reach a negative answer with
respect to the first question that we address, we do not need to
evaluate the other question for that portion of the species' range.
For Florida golden aster, we chose to evaluate the status question
first. We began by identifying portions of the range where the
biological status of the species may be different from its biological
status elsewhere in its range. For this purpose, we considered
information pertaining to the geographic distribution of individuals of
the species, the threats that the species faces, and the resiliency
condition of populations.
We evaluated the range of the Florida golden aster to determine if
the species is in danger of extinction now or likely to become so
within the foreseeable future in any portion of its range. The range of
a species can theoretically be divided into portions in an infinite
number of ways. We focused our analysis on portions of the species'
range that may meet the Act's definition of an endangered species or a
threatened species. For the Florida golden aster, we considered whether
the threats or their effects on the species are greater in any
biologically meaningful portion of the species' range than in other
portions such that the species is in danger of extinction now or likely
to become so within the foreseeable future in that portion.
We examined the following threats: development and climate change,
including cumulative effects. Currently, there are 30 known extant
Florida golden aster populations occurring in five counties
(Hillsborough, Manatee, Pinellas, Highlands, and Hardee Counties), with
25 of these populations occurring on conservation lands (Federal,
State, and conservation easements). Climate change, as discussed above,
is uniformly acting upon the species across its range, except for sea
level rise, which would only potentially affect one population at Fort
De Soto County Park in Pinellas County. As this would potentially
impact just a single population out of 30 populations, we do not
consider this concentration of threats to be at a biologically
meaningful scale.
Although development is currently concentrated in Pinellas County,
that activity would negatively impact in the foreseeable future only
five populations that occur on private lands or along roadways or
railroad lines. However, two of these populations have high and
moderate resiliency (the remaining three populations have low
resiliency), and this pattern will continue in the future. The Pinellas
County populations are currently in low condition, and some may become
extirpated within the foreseeable future due to development. Therefore,
our examination leads us to find that there is substantial information
that the Pinellas County populations may become in danger of extinction
within the foreseeable future.
We then proceeded to consider whether this portion of the range
(i.e., the Pinellas County populations) is significant. For the
purposes of this analysis, the Service is considering significant
portions of the range by applying any reasonable definition of
``significant.'' We assessed whether any portions of the range may be
biologically meaningful in terms of the resiliency, redundancy, or
representation of the entity being evaluated. This approach is
consistent with the Act, our implementing regulations, our policies,
and case law.
Currently, the Pinellas County populations represent a small
portion (less than 10 percent based on current extant populations) of
the species' range, which is not a large geographic area relative to
the range of the species. Further, these populations were all
introduced after listing (i.e., they are not naturally occurring
populations) and are not contributing much to the viability of the
species. This portion does not contribute high-quality habitat or
constitute high-value habitat for the species. In addition, this
portion does not constitute an area of habitat that is essential to a
specific life-history function for the species that is not found in the
remainder of the range. Therefore, this area does not represent a
significant portion of the species' range.
Accordingly, we find that the Florida golden aster is not in danger
of extinction now or likely to become so within the foreseeable future
in any significant portion of its range. This does not conflict with
the courts' holdings in Desert Survivors v. Department of the Interior,
321 F. Supp. 3d 1011, 1070-74 (N.D. Cal. 2018), and Center for
Biological Diversity v. Jewell, 248 F. Supp. 3d 946, 959 (D. Ariz.
2017) because, in reaching this conclusion, we did not apply the
aspects of the Final Policy on Interpretation of the Phrase
``Significant Portion of Its Range'' in the Endangered Species Act's
Definitions of ``Endangered Species'' and ``Threatened Species'' (79 FR
37578; July 1, 2014), including the definition of ``significant,'' that
those court decisions held to be invalid.
[[Page 15779]]
Determination of Status
Our review of the best available scientific and commercial data
available indicates that the Florida golden aster does not meet the
definition of an endangered species or a threatened species in
accordance with sections 3(6) and 3(20) of the Act. In accordance with
our regulations at 50 CFR 424.11(e)(2) currently in effect, Florida
golden aster does not meet the definition of an endangered or threated
species. Therefore, we are removing the Florida golden aster from the
List of Endangered and Threatened Plants.
Effects of This Final Rule
This final rule revises 50 CFR 17.12(h) by removing the Florida
golden aster from the Federal List of Endangered and Threatened Plants.
On the effective date of this rule (see DATES, above), the prohibitions
and conservation measures provided by the Act, particularly through
sections 7 and 9, will no longer apply to the Florida golden aster.
Federal agencies will no longer be required to consult with the Service
under section 7 of the Act if activities they authorize, fund, or carry
out may affect the Florida golden aster. There is no critical habitat
designated for this species, so this rule does not affect 50 CFR 17.96.
Post-Delisting Monitoring
Section 4(g)(1) of the Act requires us, in cooperation with the
States, to implement a monitoring program for not less than 5 years for
all species that have been recovered. Post-delisting monitoring (PDM)
refers to activities undertaken to verify that a species delisted due
to recovery remains secure from the risk of extinction after the
protections of the Act no longer apply. The primary goal of PDM is to
monitor the species to ensure that its status does not deteriorate, and
if a decline is detected, to take measures to halt the decline so that
proposing it as an endangered or threatened species is not again
needed. If at any time during the monitoring period, data indicate that
protective status under the Act should be reinstated, we can initiate
listing procedures, including, if appropriate, emergency listing.
We have prepared a PDM plan for Florida golden aster. The PDM plan:
(1) summarizes the status of Florida golden aster at the time of
proposed delisting; (2) describes frequency and duration of monitoring;
(3) discusses monitoring methods and potential sampling regimes; (4)
defines what potential triggers will be evaluated to address the need
for additional monitoring; (5) outlines reporting requirements and
procedures; (6) proposes a schedule for implementing the PDM plan; and
(7) defines responsibilities.
We made the draft PDM plan available for public comments with the
proposed rule published on June 24, 2021 (86 FR 33177). We did not
receive any comments on the draft PDM plan; therefore, we are adopting
the draft plan as the final plan. The final PDM plan for the species
can be found at https://www.regulations.gov under Docket No. FWS-R4-ES-
2019-0071. It is our intent to work closely with our partners towards
maintaining the recovered status of the Florida golden aster.
Required Determinations
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
Secretary's 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 have determined that no Tribes will
be affected by this final rule because no Tribal lands, sacred sites,
or resources will be affected by the removal of the Florida golden
aster from the List of Endangered and Threatened Plants.
References Cited
A complete list of references cited is available on the internet at
https://www.regulations.gov under Docket No. FWS-R4-ES-2019-0071 and
upon request from the Florida Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT, above).
Authors
The primary authors of this final rule are staff members of the
Service's Species Assessment Team and the Florida Ecological Services
Field Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Plants,
Reporting and recordkeeping requirements, Transportation, Wildlife.
Regulation Promulgation
Accordingly, we amend part 17, subchapter B of chapter I, title 50
of the Code of Federal Regulations, as set forth below:
PART 17--ENDANGERED AND THREATENED WILDLIFE AND PLANTS
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; and 4201-4245, unless
otherwise noted.
Sec. 17.12 [Amended]
0
2. In Sec. 17.12, in paragraph (h), amend the List of Endangered and
Threatened Plants by removing the entry for ``Chrysopsis floridana''
under Flowering Plants.
Stephen Guertin,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2024-04278 Filed 3-4-24; 8:45 am]
BILLING CODE 4333-15-P