Endangered and Threatened Wildlife and Plants; Threatened Species Status for Platanthera integrilabia (White Fringeless Orchid), 55304-55321 [2015-22973]
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threatened throughout an SPR, and the
population in that significant portion is
a valid DPS, we will list the DPS rather
than the entire taxonomic species or
subspecies. As stated above, we find the
New England cottontail does not
warrant listing throughout its range.
Therefore, we must consider whether
there are any significant portions of the
range of the New England cottontail.
The SPR policy is applied to all status
determinations, including analyses for
the purposes of making listing,
delisting, and reclassification
determinations. The procedure for
analyzing whether any portion is an
SPR is similar, regardless of the type of
status determination we are making.
The first step in our analysis of the
status of a species is to determine its
status throughout all of its range. If we
determine that the species is in danger
of extinction, or likely to become so in
the foreseeable future, throughout all of
its range, we list the species as an
endangered (or threatened) species and
no SPR analysis will be required. If the
species is neither in danger of extinction
nor likely to become so throughout all
of its range, we determine whether the
species is in danger of extinction or
likely to become so throughout a
significant portion of its range. If it is,
we list the species as an endangered or
a threatened species, respectively; if it is
not, we conclude that listing the species
is not warranted.
When we conduct an SPR analysis,
we first identify any portions of the
species’ range that warrant further
consideration. The range of a species
can theoretically be divided into
portions in an infinite number of ways.
However, there is no purpose to
analyzing portions of the range that are
not reasonably likely to be significant
and endangered or threatened. To
identify only those portions that warrant
further consideration, we determine
whether there is substantial information
indicating that (1) the portions may be
significant and (2) the species may be in
danger of extinction in those portions or
likely to become so within the
foreseeable future. We emphasize that
answering these questions in the
affirmative is not a determination that
the species is endangered or threatened
throughout a significant portion of its
range—rather it is a step in determining
whether a more detailed analysis of the
issue is required. In practice, a key part
of this analysis is whether the threats
are geographically concentrated in some
way. If the threats to the species are
affecting it uniformly throughout its
range, no portion is likely to warrant
further consideration. Moreover, if any
concentration of threats apply only to
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portions of the range that clearly do not
meet the biologically based definition of
‘‘significant’’ (i.e., the loss of that
portion clearly would not be expected to
increase the vulnerability to extinction
of the entire species), those portions
will not warrant further consideration.
If we identify any portions that may
be both (1) significant and (2)
endangered or threatened, we engage in
a more detailed analysis to determine
whether these standards are indeed met.
The identification of an SPR does not
create a presumption, prejudgment, or
other determination as to whether the
species in that identified SPR is
endangered or threatened. We must go
through a separate analysis to determine
whether the species is endangered or
threatened in the SPR. To determine
whether a species is endangered or
threatened throughout an SPR, we will
use the same standards and
methodology that we use to determine
if a species is endangered or threatened
throughout its range.
Depending on the biology of the
species, its range, and the threats it
faces, it may be more efficient to address
the ‘‘significant’’ question first, or the
status question first. Thus, if we
determine that a portion of the range is
not ‘‘significant,’’ we do not need to
determine whether the species is
endangered or threatened there; if we
determine that the species is not
endangered or threatened in a portion of
its range, we do not need to determine
if that portion is ‘‘significant.’’
The threats currently affecting the
New England cottontail, without
consideration for the planned or
implemented conservation efforts, are
occurring throughout the species’ range.
Habitat loss, predation, and the effects
of small population size are affecting the
species relatively uniformly across its
range. In addition, the Conservation
Strategy and its specific actions will
continue to be implemented throughout
the species’ range, and we have a high
level of certainty that those efforts will
be effective in addressing the species’
rangewide threats. Therefore, we find
that factors affecting the species are
essentially uniform throughout its
range, indicating no portion of the range
warrants further consideration of
possible endangered or threatened
status under the Act.
Our review of the best available
scientific and commercial information
indicates that the New England
cottontail is not in danger of extinction
(endangered) nor likely to become
endangered within the foreseeable
future (threatened), throughout all or a
significant portion of its range.
Therefore, we find that listing the New
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England cottontail as an endangered or
threatened species under the Act is not
warranted at this time.
We request that you submit any new
information concerning the status of, or
threats to, the New England cottontail to
our New England Field Office (see
ADDRESSES section) whenever it
becomes available. New information
will help us monitor the New England
cottontail and encourage its
conservation. If an emergency situation
develops for the New England
cottontail, we will act to provide
immediate protection.
References Cited
A complete list of references cited is
available on the Internet at https://
www.regulations.gov at Docket Number
FWS–R5–ES–2015–0136 and upon
request from the New England Field
Office (see ADDRESSES section).
Author(s)
The primary author(s) of this
document are the staff members of the
New England Field Office.
Authority
The authority for this section is
section 4 of the Endangered Species Act
of 1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: August 26, 2015.
Daniel M. Ashe,
Director, U.S. Fish and Wildlife Service.
[FR Doc. 2015–22885 Filed 9–11–15; 11:15 am]
BILLING CODE 4310–55–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R4–ES–2015–0129;
4500030113]
RIN 1018–BA93
Endangered and Threatened Wildlife
and Plants; Threatened Species Status
for Platanthera integrilabia (White
Fringeless Orchid)
Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), propose to
list Platanthera integrilabia (white
fringeless orchid), a plant species from
Alabama, Georgia, Kentucky,
Mississippi, South Carolina, and
Tennessee, as a threatened species
under the Endangered Species Act (Act).
If we finalize this rule as proposed, it
SUMMARY:
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would extend the Act’s protections to
this species.
DATES: We will accept comments
received or postmarked on or before
November 16, 2015. Comments
submitted electronically using the
Federal eRulemaking Portal (see
ADDRESSES) must be received by 11:59
p.m. Eastern Time on the closing date.
We must receive requests for public
hearings, in writing, at the address
shown in FOR FURTHER INFORMATION
CONTACT by October 30, 2015.
ADDRESSES: You may submit comments
by one of the following methods:
(1) Electronically: Go to the Federal
eRulemaking Portal: https://
www.regulations.gov. In the Search box,
enter FWS–R4–ES–2015–0129, which is
the docket number for this rulemaking.
Then, in the Search panel on the left
side of the screen, under the Document
Type heading, click on the Proposed
Rules link to locate this document. You
may submit a comment by clicking on
‘‘Comment Now!’’
(2) By hard copy: Submit by U.S. mail
or hand-delivery to: Public Comments
Processing, Attn: FWS–R4–ES–2015–
0129; U.S. Fish and Wildlife Service,
MS: BPHC, 5275 Leesburg Pike, Falls
Church, VA 22041–3803.
We request that you send comments
only by the methods described above.
We will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see Public
Comments, below, for more
information).
FOR FURTHER INFORMATION CONTACT:
Mary Jennings, Field Supervisor, U.S.
Fish and Wildlife Service, Tennessee
Ecological Services Field Office, 446
Neal Street, Cookeville, TN 38501; by
telephone 931–528–6481; or by
facsimile 931–528–7075. Persons who
use a telecommunications device for the
deaf (TDD) may call the Federal
Information Relay Service (FIRS) at
800–877–8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. Under
the Act, if we determine that a species
is an endangered or threatened species
throughout all or a significant portion of
its range, we are required to promptly
publish a proposal in the Federal
Register and make a determination on
our proposal within 1 year. Listing a
species as an endangered or threatened
species and designations and revisions
of critical habitat can only be completed
by issuing a rule.
This rule proposes the listing of
Platanthera integrilabia (white
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fringeless orchid) as a threatened
species. The white fringeless orchid is a
candidate species for which we have on
file sufficient information on biological
vulnerability and threats to support
preparation of a listing proposal, but for
which development of a listing
regulation has been precluded by other
higher priority listing activities. This
rule reassesses all available information
regarding status of and threats to the
white fringeless orchid.
This rule does not propose critical
habitat for white fringeless orchid. We
have determined that designation of
critical habitat would not be prudent for
this species because:
• Designation would increase the
likelihood and severity of illegal
collection of white fringeless orchid and
thereby make enforcement of take
prohibitions more difficult.
• This threat outweighs the benefits
of designation.
The basis for our action. Under the
Act, we may determine that a species is
an endangered or threatened species
based on any of five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. We
have determined that the threats to
white fringeless orchid consist primarily
of destruction and modification of
habitat (Factor A) resulting in excessive
shading, soil disturbance, altered
hydrology, and proliferation of invasive
plant species; collecting for recreational
or commercial purposes (Factor B);
herbivory (Factor C); and small
population sizes and dependence on
specific pollinators and fungi to
complete its life cycle (Factor E).
Existing regulatory mechanisms have
not led to a reduction or removal of
threats posed to the species from these
factors (see Factor D discussion).
We will seek peer review. We will seek
comments from independent specialists
to ensure that our designation is based
on scientifically sound data,
assumptions, and analyses. We will
invite these peer reviewers to comment
on our listing proposal.
Information Requested
Public Comments
We intend that any final action
resulting from this proposed rule will be
based on the best scientific and
commercial data available and be as
accurate and as effective as possible.
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Therefore, we request comments or
information from other concerned
governmental agencies, Native
American tribes, the scientific
community, industry, or any other
interested parties concerning this
proposed rule. We particularly seek
comments concerning:
(1) The white fringeless orchid’s
biology, range, and population trends,
including:
(a) Biological or ecological
requirements of the species, including
habitat requirements for germination,
growth, and reproduction;
(b) Genetics and taxonomy;
(c) Historical and current range,
including distribution patterns;
(d) Historical and current population
levels, and current and projected trends;
and
(e) Past and ongoing conservation
measures for the species, its habitat, or
both.
(2) Factors that may affect the
continued existence of the species,
which may include habitat modification
or destruction, overutilization, disease,
predation, the inadequacy of existing
regulatory mechanisms, or other natural
or manmade factors.
(3) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to this species
and existing regulations that may be
addressing those threats.
(4) The reasons why we should or
should not designate habitat as ‘‘critical
habitat’’ under section 4 of the Act (16
U.S.C. 1531 et seq.), including whether
there are threats to the species from
human activity, the degree of which can
be expected to increase due to the
designation, and whether that increase
in threat outweighs the benefit of
designation such that the designation of
critical habitat is not prudent.
Please include sufficient information
with your submission (such as scientific
journal articles or other publications) to
allow us to verify any scientific or
commercial information you include.
Please note that submissions merely
stating support for or opposition to the
action under consideration without
providing supporting information,
although noted, will not be considered
in making a determination, as section
4(b)(1)(A) of the Act directs that
determinations as to whether any
species is an endangered or threatened
species must be made ‘‘solely on the
basis of the best scientific and
commercial data available.’’
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in the
ADDRESSES section. We request that you
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send comments only by the methods
described in the ADDRESSES section.
If you submit information via https://
www.regulations.gov, your entire
submission—including any personal
identifying information—will be posted
on the Web site. If your submission is
made via a hardcopy that includes
personal identifying information, you
may request at the top of your document
that we withhold this information from
public review. However, we cannot
guarantee that we will be able to do so.
We will post all hardcopy submissions
on https://www.regulations.gov.
Comments and materials we receive,
as well as supporting documentation we
used in preparing this proposed rule,
will be available for public inspection
on https://www.regulations.gov, or by
appointment, during normal business
hours, at the U.S. Fish and Wildlife
Service, Tennessee Ecological Services
Field Office (see FOR FURTHER
INFORMATION CONTACT).
Because we will consider all
comments and information received
during the public comment period, our
final determinations may differ from
this proposal.
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Public Hearing
Section 4(b)(5) of the Act provides for
one or more public hearings on this
proposal, if requested. Requests must be
received within 45 days after the date of
publication of this proposed rule in the
Federal Register. Such requests must be
sent to the address shown in the FOR
FURTHER INFORMATION CONTACT section.
We will schedule public hearings on
this proposal, if any are requested, and
announce the dates, times, and places of
those hearings, as well as how to obtain
reasonable accommodations, in the
Federal Register and local newspapers
at least 15 days before the hearing.
Peer Review
In accordance with our joint policy on
peer review published in the Federal
Register on July 1, 1994 (59 FR 34270),
we will seek the expert opinions of at
least three appropriate and independent
specialists regarding this proposed rule.
The purpose of peer review is to ensure
that our listing determination is based
on scientifically sound data,
assumptions, and analyses. The peer
reviewers have expertise with the white
fringeless orchid’s biology, habitat,
physical or biological factors,
distribution, and status, or have general
botanical and conservation biology
expertise.
Previous Federal Action
The Act requires the Service to
identify species of wildlife and plants
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that are endangered or threatened, based
on the best available scientific and
commercial data. Section 12 of the Act
directed the Secretary of the
Smithsonian Institution to prepare a
report on endangered and threatened
plant species, which was published as
House Document No. 94–51. The
Service published a notice in the
Federal Register on July 1, 1975 (40 FR
27824), in which we announced that
more than 3,000 native plant taxa
named in the Smithsonian’s report and
other taxa added by the 1975 notice
would be reviewed for possible
inclusion in the List of Endangered and
Threatened Plants. The 1975 notice was
superseded on December 15, 1980 (45
FR 82480), by a new comprehensive
notice of review for native plants that
took into account the earlier
Smithsonian report and other
accumulated information. On November
28, 1983 (48 FR 53640), a supplemental
plant notice of review noted the status
of various taxa. Complete updates of the
plant notice were published on
September 27, 1985 (50 FR 39526),
February 21, 1990 (55 FR 6184), and
September 30, 1993 (58 FR 51144).
White fringeless orchid was first
listed as a Category 1 candidate in the
December 15, 1980, review. Category 1
candidates included taxa for which the
Service had sufficient information on
hand to support the biological
appropriateness of listing as endangered
or threatened species. The species was
reclassified as a Category 2 candidate in
the November 28, 1983, review.
Category 2 candidates included taxa for
which the Service had information
indicating that proposing to list the
species as endangered or threatened was
possibly appropriate, but for which
sufficient data on biological
vulnerability and threat were not
available. Further biological research
and field study usually was necessary to
ascertain the status of taxa in this
category.
In 1996, the Service eliminated
candidate categories (February 28, 1996;
61 FR 7596), and white fringeless orchid
was no longer a candidate until it was
again elevated to candidate status on
October 25, 1999 (64 FR 57534). The
species was also included in subsequent
candidate notices of review on October
30, 2001 (66 FR 54808), June 13, 2002
(67 FR 40657), May 4, 2004 (69 FR
24876), May 11, 2005 (70 FR 24870),
September 12, 2006 (71 FR 53756),
December 6, 2007 (72 FR 69034),
December 10, 2008 (73 FR 75176),
November 9, 2009 (74 FR 57804),
November 10, 2010 (75 FR 69222),
October 26, 2011 (76 FR 66370),
November 21, 2012 (77 FR 69994),
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November 22, 2013 (78 FR 70104), and
December 5, 2014 (79 FR 72450).
The 2011 Multi-District Litigation
(MDL) settlement agreement specified
that the Service will systematically, over
a period of 6 years, review and address
the needs of 251 candidate species to
determine if they should be added to the
Federal Lists of Endangered and
Threatened Wildlife and Plants. The
white fringeless orchid was on that list
of candidate species. Therefore, the
Service is making this proposed listing
determination in order to comply with
the conditions outlined in the MDL
agreement.
Background
Species Information
Taxonomy and Species Description
White fringeless orchid was first
recognized as a distinct taxon when D.S.
Correll (1941, pp. 153–157) described it
as a variety of Habenaria (Platanthera)
blephariglottis. C.A. Luer (1975, p. 186)
elevated the taxon to full species status.
The currently accepted binomial for the
species is Platanthera integrilabia
(Correll) Luer. The description of this
taxon at the full species level used the
common name of ‘‘monkey-face’’ (Luer
1975, p. 186), as have some other
publications (Zettler and Fairey 1990, p.
212; Zettler 1994, p. 686; Birchenko
2001, p. 9). A status survey report for
the species recognized both ‘‘white
fringeless orchid’’ and ‘‘monkeyface’’ as
common names (Shea 1992, p. 1). The
Service used the common name ‘‘white
fringeless orchid’’ when the species was
first recognized as a candidate for
listing, and we retain usage of this
common name here.
White fringeless orchid is a perennial
herb with a light green, 60-centimeters
(cm) (23-inches (in)) long stem that
arises from a tuber (modified
underground stem of a plant that is
enlarged for nutrient storage). The
leaves are alternate with entire margins
and are narrowly elliptic to lanceolate
(broadest below the middle and tapering
toward the apex) in shape. The lower
leaves are 20 cm (8 in) long and 3 cm
(1 in) wide. The upper stem leaves are
much smaller. The white flowers are
borne in a loose cluster at the end of the
stem. The upper two flower petals are
about 7 millimeters (mm) (0.3 in) long,
and the lower petal (the lip) is about 13
mm (0.5 in) long. The epithet
‘‘integrilabia’’ refers to the lack of any
prominent fringe on the margin of the
lip petal (Luer 1975, p. 186). The plants
flower from late July through
September, and the small narrow
fruiting capsule matures in October
(Shea 1992, p. 23).
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Distribution
To determine the current distribution
of white fringeless orchid, we used data
provided by Natural Heritage Programs
(NHP), housed in State agencies or
universities in each of the States in the
species’ geographic range: Alabama
Natural Heritage Program at Auburn
University (ANHP 2014); Georgia
Department of Natural Resources (GDNR
2014); Kentucky State Nature Preserves
Commission (KSNPC 2014); Mississippi
Department of Wildlife, Fisheries, and
Parks (MDWFP 2014); North Carolina
Department of Environment and Natural
Resources (NCDENR 2014); South
Carolina Department of Natural
Resources (SCDNR 2012); and
Tennessee Department of Environment
and Conservation (TDEC 2014). In
addition to NHP data, we used Shea’s
(1992, entire) Status Survey Report on
Platanthera integrilabia to determine
the species’ historical distribution.
In most cases, a mapped occurrence
in the databases maintained by the
NHPs represented a single group of
plants growing together in a patch of
suitable habitat. However, the Kentucky
NHP combined multiple groups of
plants (i.e., sub-occurrences), growing in
distinct habitat patches in close
proximity to one another, into single
occurrences. In two instances, the
Tennessee NHP also grouped several
sub-occurrences into a single
occurrence, where they were all located
in separate stream heads draining into a
single headwater stream. In describing
the current range and distribution of
white fringeless orchid, we have
adopted these groupings in those
instances where all of the suboccurrences were located within the
drainage of a single headwater stream.
In two instances, where Kentucky NHP
grouped sub-occurrences from drainages
of separate headwater streams into a
single occurrence, we split the suboccurrences into two separate
occurrences by grouping together only
those that were located within a single
headwater drainage.
Historical Distribution—As of 1991,
there were 30 extant occurrences and 13
with uncertain status, distributed among
20 counties in 5 southeastern States (see
Table 1, below). Shea (1992, pp. 14–17)
also reported on six locations with
historical occurrences and six from
which the species had been extirpated.
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As of 2015, there are records for 13
historical and 12 extirpated occurrences
in NHP databases. Accounting for two
locations that Shea (1992, pp. 11–14)
reported as extirpated and a third
reported as uncertain but now
considered to be historical, none of
which is included in NHP databases,
there are 28 occurrences that currently
are considered historical or extirpated.
In 1991, five of these were extant and
the status of five was uncertain (Shea
1992, pp. 7–14). Based on these data,
the species’ historical range included
Cobb County, Georgia; Henderson
County, North Carolina; and Roane
County, Tennessee, in addition to the 35
counties listed below in Table 1 for the
species’ range as of 2014. The species
has been extirpated completely from
North Carolina.
Shea (1992, pp. 17–18) lists additional
records from Butler County, Alabama;
Cherokee County, North Carolina;
Hamilton County, Tennessee; and Lee
County, Virginia, whose validity she
could neither verify nor refute based on
available data. Lacking sufficient data to
document the collection of white
fringeless orchid from Lee County, the
authors of the Flora of Virginia did not
include the species (Townsend 2012,
pers. comm.). Lacking any substantive
data for white fringeless orchid’s
historical presence in the other three
counties above, we also consider them
to not be part of the species’ historical
range.
Current Distribution—Using available
data, we categorized the current status
of each occurrence as extant, extirpated,
historical, or uncertain. Extant
occurrences are those for which recent
(i.e., since ca. 2000) observations of
flowering plants are available to confirm
the species’ persistence at a given site,
or from which material was collected
and cultivated in a greenhouse to
produce flowering specimens
confirming the identification of
vegetative plants that were observed in
the field. Because white fringeless
orchid commonly occurs with three
congeners (species belonging to the
same genus) that share similar leaf
characteristics, conclusive identification
in the absence of flowering specimens is
not possible. Extirpated occurrences are
those where the species’ absence is
considered to be certain due to lack of
recent observations of flowering white
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fringeless orchids, or vegetative plants
of any species of Platanthera, associated
with modification of the habitat to an
unsuitable condition for white fringeless
orchid. White fringeless orchid was last
seen flowering at one extirpated
occurrence as recently as 2004, but
habitat in this former transmission line
right-of-way is no longer maintained
and has become unsuitable due to
woody vegetation encroachment.
Similarly, recent observation of
flowering white fringeless orchids or
vegetative plants of any species of
Platanthera is lacking for historical
occurrences, but the habitat has not
been visibly altered at these locations.
We have assigned uncertain status to
occurrences where recent observation of
flowering white fringeless orchids is
lacking, but where basal leaves of nonflowering Platanthera spp. orchids
typically have been observed during one
or more recent visits. In addition, we
have assigned uncertain status to one
Mississippi occurrence, where a single
white fringeless orchid was seen
flowering in 2011, because the
hydrology at this site was subsequently
altered by a drainage ditch and the
species’ persistence at this site is now
questionable.
The white fringeless orchid’s
distribution is concentrated in the
Cumberland Plateau section of the
Appalachian Plateaus physiographic
province, with isolated populations
scattered across the Blue Ridge,
Piedmont, and Coastal Plain provinces
(Fenneman 1938, pp. 68, 134–137, 172,
333–334). The species is currently
extant at 58 occurrences distributed
among 32 counties, spanning 5
southeastern States (Table 1). There are
an additional 22 occurrences (Table 1)
whose current status is uncertain, which
include one additional State and three
additional counties. We consider the
species’ current distribution to include
the 6 States and 35 counties where NHP
database records for these extant and
uncertain occurrences exist (Table 1).
We included records of uncertain status
in defining the species’ current
distribution to ensure that all relevant
State and local governments and private
stakeholders are aware of white
fringeless orchid’s potential presence
and opportunities for conserving the
species and its habitat.
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TABLE 1—COUNTY-LEVEL DISTRIBUTION OF EXTANT AND UNCERTAIN STATUS WHITE FRINGELESS ORCHID OCCURRENCES, CIRCA 1991 (SHEA 1992) AND 2014 (ANHP 2014, GDNR 2014, KSNPC 2014, MDWFP 2014, NCDENR
2014, SCDNR 2012, TDEC 2014)
1991
State
2014
County
Extant
Alabama ..........................................................................
Georgia ............................................................................
Kentucky ..........................................................................
Mississippi .......................................................................
South Carolina ................................................................
Tennessee .......................................................................
Total .........................................................................
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More occurrences are included in the
species’ current distribution than were
historically known to exist, likely as a
result of increased survey effort having
been devoted to white fringeless orchid
due to its status as a candidate for
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Uncertain
Extant
Uncertain
Calhoun ..............................
Clay ....................................
Cleburne .............................
DeKalb ...............................
Jackson ..............................
Marion ................................
Tuscaloosa .........................
Winston ..............................
Bartow ................................
Carroll .................................
Chatooga ............................
Cobb ...................................
Coweta ...............................
Forsyth ...............................
Pickens ...............................
Rabun .................................
Stephens ............................
Laurel .................................
McCreary ............................
Pulaski ................................
Whitley ...............................
Alcorn .................................
Itawamba ............................
Tishomingo .........................
Greenville ...........................
Bledsoe ..............................
Cumberland ........................
Fentress .............................
Franklin ..............................
Grundy ...............................
Marion ................................
McMinn ...............................
Polk ....................................
Scott ...................................
Sequatchie .........................
Van Buren ..........................
....................
....................
....................
....................
....................
1
1
1
....................
2
....................
1
1
....................
....................
1
1
....................
4
1
....................
....................
....................
....................
1
....................
....................
....................
3
5
2
1
....................
....................
2
2
....................
1
....................
....................
....................
....................
....................
....................
....................
....................
....................
....................
....................
1
....................
....................
....................
....................
....................
1
....................
....................
....................
....................
....................
2
....................
....................
2
5
....................
....................
....................
....................
1
....................
2
1
1
1
....................
1
1
1
1
2
1
....................
1
1
1
1
1
2
2
2
1
....................
2
1
....................
2
1
2
5
4
8
1
1
1
1
5
....................
....................
....................
....................
1
2
....................
....................
....................
....................
....................
....................
....................
....................
....................
....................
....................
2
1
....................
....................
1
1
1
1
1
....................
....................
5
4
....................
....................
....................
....................
1
1
............................................
30
13
58
22
Federal listing. However, low numbers
of flowering plants have been observed
at most sites (Figure 1). For example,
fewer than 50 flowering plants have
ever been observed at one time at 45 (64
percent) of the 70 extant and uncertain
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occurrences for which data are
available. At 26 (37 percent) of these
occurrences, fewer than 10 flowering
plants have ever been recorded.
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There are 32 extant occurrences that
are located entirely, or in part, on lands
owned or managed by local, State, or
Federal government entities (Table 2). In
addition, there are seven uncertain, five
extirpated, and two historical
occurrences that are similarly situated.
Two additional occurrences, one extant
and one uncertain, are located on
private lands that are protected by
conservation easements.
TABLE 2—STATUS AND NUMBER OF WHITE FRINGELESS ORCHID OCCURRENCES ON PUBLICLY OWNED OR MANAGED
LANDS
[Note: One site is on privately owned lands that GDNR leases for use as a wildlife management area]
Extant
Uncertain
Extirpated
Historical
National Park Service ......................................................................................................
U.S. Forest Service .........................................................................................................
U.S. Fish and Wildlife Service .........................................................................................
Alabama Department of Conservation and Natural Resources ......................................
Georgia Department of Natural Resources .....................................................................
Kentucky State Nature Preserves Commission ..............................................................
Mississippi Department of Fish, Wildlife, and Parks .......................................................
North Carolina Plant Conservation Program ...................................................................
South Carolina State Parks .............................................................................................
Tennessee Department of Transportation .......................................................................
Tennessee Division of Forestry .......................................................................................
Tennessee State Parks ...................................................................................................
Tennessee Wildlife Resources Agency ...........................................................................
Forsyth County, Georgia .................................................................................................
3
9
2
....................
2
1
1
....................
....................
1
7
5
1
....................
....................
3
....................
1
....................
....................
....................
....................
1
....................
....................
1
....................
1
....................
3
....................
....................
....................
....................
....................
1
....................
....................
....................
....................
1
....................
....................
....................
....................
....................
....................
1
....................
....................
....................
....................
....................
1
....................
....................
Total ..........................................................................................................................
31
8
5
2
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Habitat
In Correll’s (1941, pp. 156–157)
description of white fringeless orchid as
a distinct variety, he included notes
from herbarium specimens that describe
the species’ habitat variously as ‘‘bog,’’
‘‘boggy sphagnum ravine,’’ ‘‘sphagnum
bog,’’ ‘‘grassy swamps,’’ and ‘‘marshy
ground.’’ Luer (1975, p. 186) described
the habitat as ‘‘. . . the deep shade of
damp deciduous forests . . . in the
thick leaf litter and sphagnum moss
along shallow wet ravines and
depressions.’’ Zettler and Fairey (1990,
p. 212) observed the species growing in
‘‘shaded and level bogs, swamps or
seepage slopes usually containing
Sphagnum.’’ Shea (1992, p. 19)
described the habitat as ‘‘wet, flat, boggy
areas at the head of streams or on
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seepage slopes . . . with Sphagnum
. . . usually grows in partial shade.’’
Hoy (2012, p. 53) demonstrated that
precipitation was the primary
hydrologic source for three wetlands at
a white fringeless orchid site on the
Cumberland Plateau in Kentucky, which
was commonly referred to as a seep.
Thus, describing many of the sites
where white fringeless orchid occurs as
‘‘seeps’’ or ‘‘seepage slopes’’ may
contradict the typical characterization of
seeps as wetlands where water from
subsurface sources emerges at the
surface (Soulsby et al. 2007, p. 200). The
term ‘‘bogs’’ refers to a specific wetland
type that accumulates peat, lacks
significant inflow or outflow, and
harbors mosses adapted to acidic
environments, particularly Sphagnum
(Mitsch and Gosselink 2000, p. 41). Peat
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is fibric organic soil material, meaning
that some plant forms incorporated into
the soil are identifiable (U.S.
Department of Agriculture, Natural
Resources Conservation Service 2006, p.
32). However, despite the common
usage of the terms ‘‘bog’’ or ‘‘boggy’’ to
describe them and the nearly ubiquitous
presence of Sphagnum spp. (sphagnum
moss) in them, the wetlands that white
fringeless orchid inhabits occur on
mineral soils and do not accumulate
peat. Further, they often are located at
stream heads and connected to
ephemeral streams via dispersed sheet
flow or concentrated surface flow in
incipient channels.
Weakley and Schafale (1994, pp. 164–
165) commented on the discrepancy
between regional use of the terms
‘‘bogs’’ and ‘‘fens’’ to describe non-
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alluvial wetlands of the Southern Blue
Ridge in which sphagnum moss is
prominently featured and their more
traditional usage in peatland
classifications. Noting that most of the
region’s non-alluvial wetlands lacked
organic soils, these authors nonetheless
chose to maintain the regional usage of
these terms in their classification, to
emphasize differences in sources of
hydrology and their effects on water
chemistry (nutrient-poor precipitation
in ‘‘bogs’’ versus mineral-rich
groundwater seepage in ‘‘fens’’). Similar
to the non-alluvial wetlands of the
Southern Blue Ridge, further study is
needed to characterize the range of
variation in soils, hydrology,
physicochemistry, and origin of
wetlands throughout the range of white
fringeless orchid.
Most sites where white fringeless
populations exist are on soils formed
over sandstone bedrock, which usually
are low in fertility and organic matter
content and are acidic (Shea 1992, p.
20). The species often occurs in swamps
dominated by Acer rubrum (red maple)
and Nyssa sylvatica (blackgum), where
common shrubs and woody vines
include Alnus serrulata (smooth alder),
Decumaria barbara (climbing
hydrangea), Smilax spp. (greenbrier),
and Viburnum nudum (possumhaw).
Common herbaceous associates of white
fringeless orchid include Doellingeria
umbellata (parasol flat-top white aster),
Gymnadeniopsis clavellata (green
woodland orchid), Lobelia cardinalis
(cardinal flower), Lycopus virginicus
(Virginia bugleweed), Osmunda
cinnamomea (cinnamon fern), O. regalis
(royal fern), Oxypolis rigidior (stiff
cowbane), Parnassia asarifolia
(kidneyleaf grass of parnassus),
Platanthera ciliaris (yellow fringed
orchid), P. cristata (crested yellow
orchid), Sphagnum spp. (sphagnum
moss), Thelypteris noveboracensis (New
York fern), Viola primulifolia (primroseleaf stemless white violet), and
Woodwardia areolata (chainfern)
(Zettler and Fairey 1990, p. 213; Shea
1992, p. 22; Patrick 2012, pers. comm.).
Sites located in powerline rights-of-way
share many of the herbaceous taxa listed
above, but lack a canopy or welldeveloped shrub stratum due to
vegetation management. Nomenclature
follows the Integrated Taxonomic
Information System (retrieved on
January 16, 2015, from the Integrated
Taxonomic Information System online
database, https://www.itis.gov).
Biology
Orchid seeds are dust-like and lack an
endosperm (the tissue produced inside
seeds of most flowering plants that
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provides nutrient reserves) making them
dependent upon acquiring carbon from
an external source (Yoder et al. 2010, p.
7). Like most terrestrial orchids, white
fringeless orchid depends on a
symbiotic (interdependent) relationship
with mycorrhizal fungi (an association
of a fungus and a plant in which the
fungus lives within or on the outside of
the plant’s roots) to enhance seed
germination and promote seedling
development and establishment (Zettler
and McInnis 1992, pp. 157–160;
Rasmussen and Whigham 1993, p.
1374). In addition to providing a carbon
source for seedling development,
mycorrhizal fungi enhance germination
by promoting increased water uptake by
orchid seeds (Yoder et al. 2000, 149).
Their small size permits dispersal of
orchid seeds to new environments via
wind currents; however, very few of the
seeds likely encounter suitable habitats
where host fungi are present (Yoder et
al. 2010, pp. 14–16). This likelihood is
further reduced in the case of species
such as white fringeless orchid, which
may rely on a single fungal host species,
Epulorhiza inquilina, to complete its life
cycle (Currah et al. 1997, p. 340).
White fringeless orchid has a selfcompatible breeding system, allowing
individuals to produce seed using their
own pollen; however, the proportions of
fruits produced through self-pollination
versus cross-pollination are not known
(Zettler and Fairey 1990, p. 214). Rates
of fruit set, measured as the proportion
of individual flowers that produced
capsules, varied in studies of
populations in Georgia (6.9 percent),
South Carolina (20.3 percent) (Zettler
and Fairey 1990, p. 214), and Tennessee
(56.9 percent) (Zettler et al. 1996, p. 20).
While these observations were made at
these populations in different years, the
Tennessee population, where
pollination was observed, is
considerably larger than the Georgia or
South Carolina populations, where no
pollination was observed. Zettler et al.
(1996, p. 22) reasoned that inbreeding
depression was a likely cause for the
lower fruit set in the smaller
populations, noting that in a separate
study both germination rates and
propagation success were greater in
white fringeless orchid seeds collected
from the largest of these populations
(Zettler and McInnis 1992, p. 160). They
speculated that higher rates of fruit set
were probably more typical historically,
when larger populations provided
greater opportunities for crosspollination to occur.
White fringeless orchid is capable of
prodigious seed production, which
might help to compensate for the likely
dispersal of many seeds into unsuitable
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habitats. In the Tennessee population
studied by Zettler et al. (1996, p. 20),
more than half of the flowers on
inflorescences (the complete flower
head of a plant including stems, stalks,
bracts, and flowers) set fruit, resulting in
a mean of 4.7 capsules per plant. The
capsules produced an average of 3,433
seeds each, indicating that each
inflorescence averaged over 16,000
seeds. With 577 inflorescences counted
in the study area, Zettler et al. (1996, p.
20) estimated that over 9,000,000 seeds
were produced. However, in separate
studies of in vitro and in situ seedling
development, even with fungal
inoculation less than 3 percent of seeds
developed into protocorms (young
seedlings) that could be established on
soil (Zettler and McInnis 1992, pp. 157–
160; Zettler 1994, pp. 65).
Known pollinators for white
fringeless orchid include three diurnal
species from two families of butterflies
(Lepidoptera): Silver spotted skipper
(Hesperiidae: Epargyreus clarus),
spicebush swallowtail (Papilionidae:
Papilio troilus), and eastern tiger
swallowtail (Papilionidae: P. glaucus)
(Zettler et al. 1996, p. 16). Based on
floral characteristics, including white
flowers and a long nectiferous (nectar
bearing) spur, as well as pollinaria
morphology in relation to potential
pollinator morphology, it is likely that
more effective pollinators for white
fringeless orchid exist in the nocturnal
sphingid moth family (Lepidoptera:
Sphingidae) (Zettler et al. 1996, pp. 17–
18); however, this has not been
confirmed. Pollinaria are the pollenbearing structure on orchids, consisting
of pollen masses (pollinia) attached to a
stalk that has a sticky pad (viscidium),
which attaches the pollinaria to
pollinators (Argue 2012, p. 5). Despite
the fact that nectar concentrations in
white fringeless orchid flowers did not
fluctuate significantly over a 24-hour
observation period, Zettler et al. (1996,
p. 20) noticed the floral fragrance
produced by a large Tennessee
population intensified between the
hours of 7:00 p.m. and 11:00 p.m.,
suggesting the species possesses
adaptions for attracting nocturnal
pollinators.
Genetics
Birchenko (2001, pp. 18–23, 47–48)
analyzed genetic structure among 25
white fringeless orchid populations,
distributed across Alabama, Georgia,
Tennessee, and Kentucky. Her
‘‘populations’’ corresponded to specific
NHP occurrences. The majority (79
percent) of the genetic variation was
present as variation within populations,
while 21 percent of the variation was
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attributable to differences between
populations (Birchenko 2001, p. 29).
While these results alone do not
demonstrate that genetic variability in
white fringeless orchid populations has
been eroded by restricted gene flow,
Birchenko (2001, pp. 34–40) cautioned
that interactions between demographic
and ecological factors could be a cause
for some observed population declines
and could ultimately cause declines in
the species’ genetic variation and
increase differentiation among white
fringeless orchid populations.
mstockstill on DSK4VPTVN1PROD with PROPOSALS
Summary of Factors Affecting the
Species
Under section 4(a)(1) of the Act, we
may list a species based on: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. Listing
actions may be warranted based on any
of the above threat factors, singly or in
combination.
Information pertaining to white
fringeless orchid in relation to the five
factors provided in section 4(a)(1) of the
Act is discussed below. In considering
what factors might constitute threats, we
must look beyond the mere exposure of
the species to the factor to determine
whether the species responds to the
factor in a way that causes actual
impacts to the species. If there is
exposure to a factor, but no response, or
only a positive response, that factor is
not a threat. If there is exposure and the
species responds negatively, the factor
may be a threat, and we then attempt to
determine if that factor rises to the level
of a threat, meaning that it may drive or
contribute to the risk of extinction of the
species such that the species warrants
listing as an endangered or threatened
as those terms are defined by the Act.
This does not necessarily require
empirical proof of a threat. The
combination of exposure and some
corroborating evidence of how the
species is likely impacted could suffice.
The mere identification of factors that
could impact a species negatively is not
sufficient to compel a finding that
listing is appropriate; we require
evidence that these factors are operative
threats that act on the species to the
point that the species meets the
definition of an endangered or
threatened species under the Act.
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Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Habitat modification caused by
development, silvicultural practices,
invasive plant species, disturbance by
feral hogs, shading due to understory
and canopy closure, altered hydrology,
and right-of-way maintenance have
impacted the range and abundance of
white fringeless orchid.
Development
One white fringeless orchid
occurrence was extirpated from a site in
Henderson County, North Carolina,
which Shea (1992, p. 15) reported had
been nearly completely destroyed by
construction of a building. Another
occurrence in Tishomingo County,
Mississippi, was extirpated from a site
that was disturbed by construction of
the Yellow Creek Nuclear Power Plant
(Shea 1992, p. 15). A third site from
which the species is considered
extirpated, in Roane County, Tennessee,
was severely disturbed during highway
construction (Shea 1992, p. 15). One
extant occurrence in Carroll County,
Georgia, is located within a subdivision
where restrictions have been put in
place to protect the wetland habitat.
Another extant occurrence in Pickens
County, Georgia, is located within a
subdivision, but the wetland habitat
where white fringeless orchid occurs is
located within an area protected by a
conservation easement held by the
North American Land Trust. There is
one occurrence of uncertain status that
is located on an as yet undeveloped lot
in a subdivision in Grundy County,
Tennessee. Potential future residential
development at this site could directly
impact white fringeless orchid due to
habitat conversion or ground
disturbance, or could indirectly affect
the species by altering hydrology,
increasing shading, or introducing
invasive, nonnative plants.
Based on our review of the best
commercial and scientific data
available, development is a threat of low
magnitude with potential to affect few
white fringeless orchid populations in
the foreseeable future.
Silvicultural Practices
Direct and indirect effects of
silvicultural practices have adversely
affected habitat conditions and
abundance of many white fringeless
orchid populations. Incompatible
silviculture has taken the form of
clearcutting, both of swamps occupied
by the species and of surrounding
upland forests. Shea (1992, p. 15)
reported that white fringeless orchid
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55311
had been extirpated from two Alabama
sites where logging had disturbed the
habitat. At one of these sites, the loss
was attributed to impacts from logging
and removal of beaver dams.
While white fringeless orchid has
sometimes shown short-term increases
in flower production following canopy
removal, the longer-term response
typically is a decline in abundance as
vegetation succession ensues (Shea
1992, pp. 26, 96; Birchenko 2001, p. 33).
Forests have been clearcut at nine extant
occurrences and two of uncertain status
in Tennessee, two extant sites and one
of uncertain status in Alabama, and one
extant site in Georgia. Of these, there is
evidence for declines in white fringeless
orchid abundance following timber
harvests at five extant occurrences and
two of uncertain status in Tennessee
(TDEC 2014) and one extant occurrence
in Alabama (Birchenko 2001, p. 33;
ANHP 2014). At some sites, the timber
harvests were too recent to know yet
how white fringeless orchid will
respond.
In many cases, native forests
surrounding white fringeless orchid
sites have been clearcut and replaced by
intensively managed pine plantations,
often consisting solely of Pinus taeda
(loblolly pine), where intensive
mechanical or chemical site preparation
before planting occurs in order to
reduce seedling competition with other
tree species (Clatterbuck and Ganus
1999, p. 4). Plantation forestry generally
causes reductions in streamflow as
compared to native forest vegetation
(Scott 2005, p. 4204), and research from
the Cumberland Plateau comparing
calcium stores in soils and trees of
native hardwood forests to mature pine
on converted hardwood sites revealed
calcium loss from the system after a
single pine rotation that could impede
future regrowth of the native oakhickory forest (McGrath et al. 2004, p.
21). The fact that plantation forests are
implicated in reduced streamflow
suggests that they could reduce the
hydroperiod (seasonal pattern of the
water level that results from the
combination of the water budget and the
storage capacity of a wetland) in
wetlands located at the heads of
streams, such as those typically
occupied by white fringeless orchids,
when they are embedded in a matrix of
pine plantations. While more
information on indirect effects of pine
plantations on hydroperiods of wetlands
occupied by white fringeless orchid is
needed, evidence suggests that restoring
native hardwood forest vegetation may
be needed to restore wetland hydrology
in some sites, and that this would be a
challenging and long-term process.
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At least four extant occurrences in
Alabama, two in Georgia, and four in
Tennessee are located in wetlands that
are either located in pine plantations or
bordered by them in surrounding
uplands; one Tennessee occurrence of
uncertain status is similarly situated.
Fourteen percent of native forest, in
seven counties of the southern
Cumberland Plateau in Tennessee that
are occupied by white fringeless orchid,
was lost between 1981 and 2000. The
majority (74 percent) of this lost native
forest was converted to nonnative
loblolly pine plantations, and the
annual rate of conversion doubled
during the last 3 years (1997–2000)
(McGrath et al. 2004, p. 13). Given that
there are three extant Tennessee
occurrences and two of uncertain status
that are located on private industrial
forest lands, which have not yet been
converted to nonnative pine plantations,
conversion of lands surrounding
additional white fringeless orchid
occurrences represents a foreseeable
future threat to the species.
Based on our review of the best
commercial and scientific data
available, silvicultural practices are a
threat of moderate magnitude to white
fringeless orchid populations.
Invasive Plant Species
The presence of invasive, nonnative
plant species, including Microstegium
vimineum (Japanese stiltgrass),
Ligustrum sinense (Chinese privet), and
Perilla frutescens (beefsteak plant), has
been documented at 10 extant white
fringeless orchid occurrences and one of
unknown status (U.S. Forest Service
(USFS) 2008, p. 53; Richards 2013, pers.
comm.; KSNPC 2014; TDEC 2014).
Chinese privet has been negatively
correlated with cover, abundance, and
richness of native herbaceous species in
riparian wetlands of the Piedmont
physiographic province (Greene and
Blossey 2012, p. 143). Japanese stiltgrass
has been shown to increase pH and
phosphorous availability in Cumberland
Plateau forest soils (McGrath and
Binkley 2009, pp. 145–153) and to
increase abundance of vesicular
arbuscular mycorrhiza (VAM;
mycorrhizal fungi that grow into the
roots of host plants and form specialized
structures called arbuscules and
vesicles) in other sandstone-derived
soils (Kourtev et al. 2002, p. 3163) as
compared to native vegetation. While
the effect of these soil alterations on
white fringeless orchid has not been
investigated, the species is associated
with acidic (i.e., lower pH) soils (Zettler
and Fairey 1990, p. 213) and is
dependent upon a specific mycorrhizal
fungus that is not a VAM (Currah et al.
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1997, p. 340). To the extent that
increases in VAM might lead to
decreases in abundance of the orchid’s
mycorrhizal fungus, Epulorhiza
inquilina, negative effects on
germination and growth would be
expected for white fringeless orchid.
In addition to threats posed by
nonnative plant species, at two extant
white fringeless orchid sites, a native
species, Lygodium palmatum (American
climbing fern), has demonstrated
invasive tendencies. Both sites are on
public lands, and USFS attempts to
control spread of the species at one of
the sites met limited success. At the site
on National Park Service lands,
American climbing fern blankets
vegetation along both sides of a dirt road
that is in close proximity to a white
fringeless orchid site, and the fern vines
have spread into adjacent forests,
including the wetland where white
fringeless orchid occurs. Left
unmanaged, encroachment of nonnative
plants and American climbing fern
could reduce potential for exposure of
seeds to light before being incorporated
into the soil, which enhances
germination rates (Zettler and McInnis
1994, p. 137).
Based on available data,
encroachment by native and nonnative
invasive plants is a threat of moderate
magnitude to white fringeless orchid
populations.
Feral Hogs
Ground disturbance by rooting of feral
hogs has been observed at 13 extant
white fringeless orchid occurrences, in
Georgia and Tennessee, including two
of the largest known occurrences, both
on protected lands (Zettler 1994, p. 687;
USFS 2008, p. 54; Richards 2013 pers.
comm.; Richards 2014, pers. comm.;
Tackett 2015, pers. comm.). These
disturbances have affected specific
microsites where white fringeless orchid
had previously been observed growing,
as well as surrounding wetland habitat.
Disturbance by feral hogs has been
shown to affect plant communities by
causing decreases in plant cover,
diversity, and regeneration; effects to
fungi from feral hogs are also known to
occur (Barrios-Garcia and Ballari 2012,
p. 2295), suggesting potential for
adverse effects to white fringeless
orchid via disruption of the symbiotic
interactions with mycorrhizal fungi that
enhance seed germination and promote
seedling development and
establishment (Zettler and McInnis
1992, pp. 157–160; Rasmussen and
Whigham 1993, p. 1374).
Based on our review of the best
commercial and scientific data
available, feral hogs are a threat of
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moderate magnitude to white fringeless
orchid populations.
Excessive Shading
Despite the fact that white fringeless
orchid habitat has been described as
shaded (Luer 1975, p. 186; Zettler and
Fairey 1990, p. 212; Shea 1992, p. 19),
excessive shading due to vegetation
succession has been recognized as a
factor associated with population
declines (Shea 1992, pp. 26, 55, 61, 69;
Richards 2013, pers. comm.; Schotz
2015, p. 4), and succession of woody
vegetation has been named as the
primary factor in the decline of
Tennessee populations (TDEC 2012, p.
3). One Tennessee occurrence was
extirpated due to woody vegetation
succession in a right-of-way that
occurred following removal of a
powerline (TDEC 2014). Available data
indicate that this threat has been noted
at 19 extant occurrences and 5 of
uncertain status across the species’
geographic range (Richards 2013, pers.
comm.; Sullivan 2014, pers. comm.;
KSNPC 2014; TDEC 2014; Schotz 2015,
pp. 10–35). The threat of shading has
been most often noted in instances
where woody succession followed
logging in or adjacent to sites occupied
by white fringeless orchid. As noted
above, white fringeless orchid
occurrences often exhibit short-term
increases in flower production
following canopy removal, but the
longer-term response typically is a
decline in abundance as woody
vegetation succession ensues (Shea
1992, pp. 26, 96; Birchenko 2001, p. 33;
TDEC 2012, pp. 2–3). It has been
suggested that fire could play a role in
regulating woody vegetation growth in
uplands surrounding white fringeless
orchid habitats, allowing greater light
penetration into swamps where the
species grows (Schotz 2015, p. 4).
Based on our review of the best
commercial and scientific data
available, excessive shading is a threat
of moderate magnitude to white
fringeless orchid populations.
Altered Hydrology
Several factors have been identified as
causes for altered hydrology in white
fringeless orchid habitat, including
pond construction (TDEC 2008, p. 4),
ditching (Sullivan 2014, pers. comm.),
development, logging (Shea 1992, p. 26;
Taylor 2014, pers. comm.), and woody
vegetation succession following logging
(Hoy 2012, p. 13). In Tennessee, three
white fringeless orchid sites have been
destroyed by pond construction, one as
recently as 2006 (TDEC 2008, p. 4). One
site in Cobb County, Georgia, was
destroyed by pond construction
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(Richards 2014, pers. comm.). In
Winston County, Alabama, hydrology
was altered by the removal of beaver
dams to facilitate a logging operation,
causing the extirpation of a white
fringeless orchid occurrence (Shea 1992,
p. 25).
Altered hydrology has been noted as
a threat at five extant occurrences and
four of unknown status (Taylor 2014,
pers. comm.; Sullivan 2014, pers.
comm.; GDNR 2014; KSNPC 2014;
TDEC 2014). Conversion of surrounding
uplands to a pine plantation was noted
as the cause for hydrologic alteration at
one extant site in Georgia (GDNR 2014),
and as noted above, is a condition that
is present at nine other extant
occurrences and one of unknown status.
Logging in surrounding uplands is
suspected of contributing to altered
hydrology at two Kentucky occurrences,
one extant and one of uncertain status
(Taylor 2014, pers. comm.; KSNPC
2014), by causing increased surface
runoff during heavy precipitation events
and accelerating channel development
in wetlands at stream heads. In addition
to loss of white fringeless orchid habitat
and occurrences due to pond
construction at the three Tennessee sites
discussed above, hydrology has been
altered in wetland habitats down slope
of ponds at two other Tennessee sites,
where white fringeless orchid’s status is
now uncertain (TDEC 2014). In
Mississippi, ditching has altered
hydrology at a site where white
fringeless orchid was discovered in
2011, leaving the species’ status
uncertain at this location (Sullivan
2014, pers. comm.). Ditching has also
altered hydrology at an extant
occurrence located adjacent to a State
highway in Tennessee. Disturbance by
heavy equipment in an adjacent
powerline right-of-way is thought to
have altered hydrology at an extant site
in Kentucky, by causing rutting of soils
and hastening channel development at
the stream head (Taylor 2014, pers.
comm.).
While most observations of threats
related to logging activity have
concerned habitat disturbance or
increased shading caused by woody
vegetation regrowth, Hoy (2012, p. 26)
suggests that high stem densities that
occur during succession following
canopy removal shorten the
hydroperiod of wetlands at an extant
white fringeless orchid site in Kentucky.
This results from increased
evapotranspiration, due to greater leaf
surface area, causing faster rates of
water loss. While only empirically
documented in wetlands where a single
white fringeless orchid occurrence is
located, this process likely has affected
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numerous other sites where canopy
removal has occurred due to logging.
Based on our review of the best
commercial and scientific data
available, altered hydrology is a threat
of moderate magnitude to white
fringeless orchid populations.
Right-of-Way Maintenance
Eleven extant white fringeless orchid
occurrences and one of uncertain status
are located in transportation or utility
rights-of-way (Richards 2013, pers.
comm.; KSNPC 2014; TDEC 2014).
Vegetation management practices in
such habitats prevent advanced
succession of woody vegetation, which
can benefit white fringeless orchid by
periodically reducing shading. On the
other hand, mechanical clearing in these
habitats can alter hydrology by causing
rutting of soils and hastening channel
development, as discussed in the
preceding section (Taylor 2014, pers.
comm.). Mowing during the flowering
period for white fringeless orchid is
detrimental, given the low flowering
rates that have been observed in this
species and the fact that individual
plants will not regenerate flowers
during a growing season once they are
lost to herbivory or other causes
(Sheviak 1990, p. 195). Also, it is likely
that indiscriminate herbicide
application would cause mortality of
white fringeless orchid plants. However,
we have knowledge of one event in
which the species responded favorably
following selective herbicide
application to control woody plant
succession in a Tennessee Valley
Authority transmission line right-ofway, reaching record numbers of
flowering plants documented at the site
within 2 years following the herbicide
treatment. The lack of adverse effect to
white fringeless orchid in this instance
is likely attributable to the targeted
application of herbicides to woody
plants only.
Based on our review of the best
commercial and scientific data
available, right-of-way maintenance is a
threat of moderate magnitude to white
fringeless orchid populations.
Conservation Efforts To Reduce Habitat
Destruction, Modification, or
Curtailments of Its Range
The USFS has undertaken efforts to
restore or protect habitat at a number of
white fringeless orchid sites located on
National Forest (NF) lands. At the
Cherokee NF, the USFS constructed
fences to exclude feral hogs at two sites,
one of which is the largest known
occurrence of the species. These fences
are effective when maintained; however,
only the main concentration of plants is
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protected at the site where the largest
occurrence is present. At the Daniel
Boone NF, the installation of check
dams (small, often temporary, dam
constructed across a swale, drainage
ditch, or waterway to counteract erosion
by reducing water flow velocity) in 2005
has been somewhat effective in restoring
suitable conditions for white fringeless
orchid at a site where wetland
hydrology had been altered. Efforts to
control invasion by Japanese stiltgrass
by repeatedly weeding at one site on
Daniel Boone NF have been hampered
by a seed source that exists on private
lands upslope of the site (Taylor 2014,
pers. comm.).
Efforts have been made to restore
suitable habitat conditions at one site on
KSNPC lands, by reducing woody stem
encroachment in 2012, following a
timber harvest, and by placing log dams
to slow surface runoff and minimize
channel development. To date, white
fringeless orchid has not shown a
measureable response to this
management effort; despite large
numbers of vegetative Platanthera spp.
leaves being present, fewer than 30
flowering plants per year have been
observed in recent years at this site,
where 530 plants were observed
flowering in 1998 (KSNPC 2014).
Summary of Factor A
The threats to white fringeless orchid
from habitat destruction and
modification are occurring throughout
much of the species’ range. These
threats include development,
silvicultural practices, invasive plant
species, disturbance by feral hogs,
shading due to understory and canopy
closure, altered hydrology, and right-ofway maintenance. While the species is
present in a number of sites on
conservation lands, few conservation
actions have been undertaken to address
these threats to the species’ habitat, and
those that are described above have met
with limited success. The populationlevel impacts of habitat destruction and
modification are expected to continue.
Threats related to silvicultural practices
could increase in the future, given that
some occurrences are located on private
industrial forest lands, where logging
and future conversion of native
hardwood forests to pine plantation are
likely to occur. In addition to physical
disturbances that alter hydrology,
predicted changes in precipitation and
drought frequency and severity (see
Factor E, below) may contribute to
increased loss of suitable habitat in the
future.
Based on our review of the best
commercial and scientific data
available, we conclude that the present
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or threatened destruction, modification,
and curtailment of its habitat or range is
currently a threat to white fringeless
orchid and is expected to continue and
possibly increase in the future.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
White fringeless orchid was first
collected from a site in McCreary
County, Kentucky, but had disappeared
from the site by the 1940s, apparently
due to the collection of hundreds of
specimens to be deposited in herbaria
(Ettman and McAdoo 1979 cited in
Zettler and Fairey 1990, p. 212). Shea
(1992, p. 27) cites personal
communications from R. Smartt and P.
Somers, the latter of whom was a
botanist with Tennessee’s Natural
Heritage Program, reporting that two
nurseries in Tennessee had collected
white fringeless orchid plants for resale.
While we are not able to independently
verify these historical reports, they
suggest that collecting for various
purposes has long been a threat to white
fringeless orchid. Evidence of recent
plant collecting (for unknown
purposes), at two separate locations, is
presented below.
The first of these occurred in 2004,
alongside a State highway in Chattooga
County, Georgia. Botanists discovered
many flowering plants at the site, but
when they later returned to the site they
found that most of the plants had been
dug out and removed. During 2014, only
a single non-flowering white fringeless
orchid was seen at this site (Richards
2014, pers. comm.). The second incident
took place during 2014, alongside a
State highway in Sequatchie County,
Tennessee. A Service biologist observed
83 flowering white fringeless orchids at
this site on August 13, 2014, but 2
weeks later only 31 plants bearing
flowers or fruiting capsules were found
during a survey with TDEC botanists. In
the location where the greatest
concentration of flowering plants had
been observed on August 13, there were
areas where mats of sphagnum moss
and roots of woody plants had been
scraped away from the surface and
shallow depressions were present in the
mineral soil beneath. Because no
wildlife tracks were present in the area
where the surface disturbance had
occurred and no partial stems were
present to indicate that the loss resulted
from herbivory, the Service and TDEC
botanists concluded that the plants had
been collected.
While the fate of plants that have been
collected is not known, we received
information about white fringeless
orchids having been purchased via an
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online vendor in 2004 (Richards 2014,
pers. comm.). The plants were sold as
nursery grown Platanthera
blephariglottis (white fringed orchid), a
taxon of which white fringeless orchid
was once treated as a variety (Correll
1941, pp. 153–157); however, when the
plants later flowered in a greenhouse, it
was apparent they were white fringeless
orchids. When the seller was questioned
about the origin of the plants, she
initially insisted they had come from a
friend’s private lands. The seller later
refused to respond to additional
inquiries from the buyer. A recent
online search for commercially
available, native Platanthera orchids
revealed that three species, which often
co-occur with white fringeless orchid,
were being offered for sale on the online
auction and shopping Web site eBay
(www.ebay.com, accessed on September
17, 2014). The unintended purchase of
white fringeless orchid from an online
vendor, combined with the offering of
three other Platanthera orchids for sale
via eBay, provides additional evidence
that demand exists for native orchids of
this genus.
Due to the species’ rarity, the small
sizes of most known populations, and
the fact that most of the populations are
located in remote sites that are
infrequently monitored by conservation
organizations or law enforcement,
collection is a threat to P. integrilabia.
In small populations, the collection of
even a few individuals would diminish
reproductive output and likely reduce
genetic diversity.
Based on our review of the best
commercial and scientific data
available, overutilization for
commercial, scientific, or recreational
purposes is currently a threat of low
magnitude to white fringeless orchid
and is expected to continue in the
future. If the Service were to publish a
proposal to designate critical habitat for
this species, which would include
detailed maps and descriptions of
locations where the species is present,
the magnitude and severity of this
activity would increase, and it would
become a threat of moderate to high
magnitude.
Factor C. Disease or Predation
Zettler and Fairey (1990, p. 214)
reported that both herbivory and disease
affected two white fringeless orchid
populations they studied in Georgia and
South Carolina. At the Georgia site, 16.5
percent of the white fringeless orchids
suffered from herbivory and 11.5
percent from disease; at the South
Carolina site, herbivory and disease
were evident on 22.5 and 23.9 percent
of the plants, respectively. The specific
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herbivores were not discussed, but
disease was attributed to pathogenic
fungi that were isolated from necrotic
tissue, including species of Alternaria,
Pestalotia, Nigrospora, and Cercospora
(Zettler and Fairey 1990, p. 214).
Zettler (1994, p. 687) also reported
observations of tuber herbivory by feral
hogs at the largest white fringeless
orchid occurrence in McMinn County,
Tennessee. The USFS constructed
fences to exclude hogs from the greatest
concentration of plants at this site and
at a smaller occurrence in Polk County,
but found the fence at the McMinn
County site in need of repair in 2002,
when they discovered that
approximately half of the flowering
white fringeless orchids and many
vegetative orchids had been uprooted
(USFS 2008, p. 54). As noted above,
evidence of feral hog disturbance has
been observed at 10 extant white
fringeless orchid sites.
Numerous observers have reported
herbivory by deer as a threat to white
fringeless orchids, specifically removal
of inflorescences from white fringeless
orchid plants (Zettler and Fairey 1990,
p. 212; Shea 1992, pp. 27, 61, 71–77,
95–97; TDEC 2012, p. 3; KSNPC 2014;
TDEC 2014). From these sources, we
found observations of inflorescence
herbivory at 21 extant occurrences and
5 where the status is now uncertain. It
is likely that this threat affects most
white fringeless orchid occurrences
(TDEC 2012, p. 3), despite not having
been specifically documented in every
instance.
Using material supplied by the
Service, TDEC biologists installed
plastic deer control fencing around two
areas with concentrations of white
fringeless orchids at a site on Tennessee
State Park lands in 2013. During 2014,
there were 105 flowering plants at the
site, plus 31 plants with browsed
inflorescences found outside of the
fenced enclosures and one browsed
plant inside one of the enclosures where
the fence had partially collapsed. Inside
of the enclosures were 45 flowering
plants that were unharmed.
Approximately one-third of the
flowering plants outside of the fenced
areas suffered inflorescence herbivory.
The high frequency at which
inflorescence herbivory has been
observed at white fringeless orchid
occurrences likely contributes to
population declines in this species.
Orchid growth is initiated each spring
from overwintered buds, similar to most
perennial plants; however, orchids
differ from most other plants by lacking
the capacity to replace tissues lost to
herbivory or other causes until the
following year. In addition, in several
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species of Platanthera, the usual
response to loss of the shoot is death of
the plant (Sheviak 1990, p. 195).
Based on our review of the best
commercial and scientific data
available, predation is a threat of
moderate to high magnitude to white
fringeless orchid and is expected to
continue in the future. Pathogenic fungi
have been documented in only two
populations, though their presence has
likely been overlooked by most
observers, and therefore they are a low
magnitude threat.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Section 4(b)(1)(A) of the Act requires
the Service to take into account ‘‘those
efforts, if any, being made by any State
or foreign nation, or any political
subdivision of a State or foreign nation,
to protect such species. . . .’’ In
relation to Factor D under the Act, we
interpret this language to require the
Service to consider relevant Federal,
State, and tribal laws, plans, regulations,
and other such mechanisms that may
minimize any of the threats we describe
in threat analyses under the other four
factors, or otherwise enhance
conservation of the species. We give
strongest weight to statutes and their
implementing regulations and to
management direction that stems from
those laws and regulations. An example
would be State governmental actions
enforced under a State statute or
constitution, or Federal action under
statute.
Having evaluated the significance of
the threat as mitigated by any such
conservation efforts, we analyze under
Factor D the extent to which existing
regulatory mechanisms are inadequate
to address the specific threats to the
species. Regulatory mechanisms, if they
exist, may reduce or eliminate the
impacts from one or more identified
threats. In this section, we review
existing State and Federal regulatory
mechanisms to determine whether they
effectively reduce or remove threats to
the white fringeless orchid.
The white fringeless orchid is listed
as special concern, with historical
status, by the State of North Carolina, as
threatened by the State of Georgia, and
as endangered by the Commonwealth of
Kentucky and State of Tennessee.
The North Carolina Plant Protection
and Conservation Act (NCPPCA; North
Carolina General Statutes 106–202)
authorizes the North Carolina Plant
Conservation Board, within the
Department of Agriculture and
Consumer Services, to among other
things: Maintain a list of protected plant
species; adopt regulations to protect,
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conserve, or enhance protected plant
species; and regulate the sale or
distribution of protected plant species.
The NCPPCA forbids any person from
uprooting, digging, taking or otherwise
disturbing or removing protected plant
species from the lands of another
without a written permit and prescribes
penalties for violations.
The law that provides official
protection to designated species of
plants in Georgia is known as the
Wildflower Preservation Act of 1973.
Under this State law, no protected plant
may be collected without written
landowner permission. No protected
plant may be transported within Georgia
without a transport tag with a permit
number affixed. Permits are also used to
regulate a wide array of conservation
activities, including plant rescues, sale
of protected species, and propagation
efforts for augmenting natural
populations and establishing new ones.
No protected plants may be collected
from State-owned lands without the
express permission of the GDNR. The
Georgia Environmental Policy Act
(GEPA), enacted in 1991, requires that
impacts to protected species be
addressed for all projects on Stateowned lands, and for all projects
undertaken by a municipality or county
if funded half or more by State funds,
or by a State grant of more than
$250,000. The provisions of GEPA do
not apply to actions of nongovernmental entities. On private lands,
the landowner has ultimate authority on
what protection efforts, if any, occur
with regard to protected plants (Patrick
et al. 1995, p. 1 of section titled ‘‘Legal
Overview’’).
The Kentucky Rare Plants Recognition
Act, Kentucky Revised Statutes (KRS),
chapter 146, sections 600–619, directs
the KSNPC to identify plants native to
Kentucky that are in danger of
extirpation within Kentucky and report
every 4 years to the Governor and
General Assembly on the conditions and
needs of these endangered or threatened
plants. This list of endangered or
threatened plants in Kentucky is found
in Kentucky Administrative
Regulations, title 400, chapter 3:040.
The statute (KRS 146:600–619)
recognizes the need to develop and
maintain information regarding
distribution, population, habitat needs,
limiting factors, other biological data,
and requirements for the survival of
plants native to Kentucky. This statute
does not include any regulatory
prohibitions of activities or direct
protections for any species included in
the list. It is expressly stated in KRS
146.615 that this list of endangered or
threatened plants shall not obstruct or
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hinder any development or use of
public or private land. Furthermore, the
intent of this statute is not to ameliorate
the threats identified for the species, but
it does provide information on the
species.
The Tennessee Rare Plant Protection
and Conservation Act of 1985 (TRPPCA;
Tennessee Code Annotated 11–26–201)
authorizes the Tennessee Department of
Environment and Conservation (TDEC)
to, among other things: Conduct
investigations on species of rare plants
throughout the State of Tennessee;
maintain a listing of species of plants
determined to be endangered,
threatened, or of special concern within
the State; and regulate the sale or export
of endangered species via a licensing
system. The TRPPCA forbids persons
from knowingly uprooting, digging,
taking, removing, damaging, destroying,
possessing, or otherwise disturbing for
any purpose, any endangered species
from private or public lands without the
written permission of the landowner,
lessee, or other person entitled to
possession and prescribes penalties for
violations. The TDEC may use the list of
threatened and special concern species
when commenting on proposed public
works projects in Tennessee, and the
department encourages voluntary efforts
to prevent the plants on this list from
becoming endangered species. This
authority is not, however, to be used to
interfere with, delay, or impede any
public works project.
Thus, despite the fact that the white
fringeless orchid is listed as special
concern, threatened, or endangered by
the States of Georgia, North Carolina,
and Tennessee and the Commonwealth
of Kentucky, these designations confer
no guarantee of protection to the
species’ habitat, whether on privately
owned or State-owned lands, unless
such protections are voluntarily
extended to the species, and only
prohibit unauthorized collection in
Georgia, North Carolina, and Tennessee.
Section 404 of the Clean Water Act
(CWA; 33 U.S.C. 1251 et seq.)
establishes a Federal program for
regulating the discharge of dredged or
fill material into waters of the United
States, including wetlands.
Additionally, section 401 of the CWA
forbids Federal agencies from issuing a
permit or license for activities that may
result in a discharge to waters of the
United States until the State or Tribe
where the discharge would originate has
granted or waived certification. All of
the States where white fringeless orchid
occurs maintain regulatory programs
providing a framework for issuance of
section 401 certifications related to
applications for section 404 permits.
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This legislation does not prohibit the
discharge of these materials into
wetlands; rather, it provides a regulatory
framework that requires permits prior to
such action being taken. The U.S. Army
Corps of Engineers (Corps) reviews
individual permits for potentially
significant impacts; however, most
discharges are considered to have
minimal impacts and may be covered by
a general permit that does not require
individual review.
Due to their typical position in nonnavigable heads of streams located
remotely from traditional navigable
waters, where flow is ephemeral or
intermittent and channels are poorly
defined, if present at all, wetlands
where white fringeless orchid occurs
have been considered to not exhibit a
significant nexus with traditional
navigable waters. Therefore, these types
of wetlands typically do not meet the
definition of waters of the United States
given in the Environmental Protection
Agency (EPA) and Corps joint
memorandum Clean Water Act
Jurisdiction Following the U.S. Supreme
Court’s Decision in Rapanos v. United
States & Carabell v. United States
(December 2, 2008). However, on June
29, 2015, the EPA and Corps published
a final rule (80 FR 37054) that revises
the definition of ‘‘Waters of the United
States.’’ Specific guidance on
implementation of this revised
definition is currently lacking, but it
appears that the revised definition now
includes the habitats where white
fringeless orchid occurs among waters
of the United States.
While the wetland habitats occupied
by white fringeless orchid are now
likely to be included within the
definition of waters of the United States,
as noted above, section 404 of the CWA
does not necessarily prevent
degradation to such habitats from the
discharge of dredge or fill material. It
simply provides a regulatory program
for permitting activities that would
result in such a discharge. Further,
discharges associated with normal
farming, ranching, and forestry
activities, such as plowing, cultivating,
minor drainage, and harvesting for the
production of food, fiber, and forest
products are exempt from the
requirement to obtain a permit. Thus,
potential impacts to wetland habitats
from silvicultural activities such as
those described above in the Factor A
discussion are not regulated under
section 404 of the CWA.
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Factor E. Other Natural or Manmade
Factors Affecting Its Continued
Existence
Small Population Size
The low number of individuals that
have been seen at most white fringeless
orchid occurrences (Figure 1, above)
increases the species’ vulnerability to
threats, discussed under Factors A
through D, above, by diminishing its
resilience to recover from demographic
reductions caused by habitat
disturbance or modification, collecting,
or herbivory. Despite the fact that white
fringeless orchid has been shown to be
self-compatible, higher rates of fruit set
have been observed in larger
populations, presumably due to higher
rates of cross-pollination (Zettler and
Fairey 1990, p. 214; Zettler et al. 1996,
p. 20). Zettler et al. (1996, p. 22)
attributed the lower fruiting rates in the
smaller populations to inbreeding
depression, noting that in a separate
study both germination rates and
propagation success were greater in
white fringeless orchid seeds collected
from the largest of the three populations
they studied (Zettler and McInnis 1992,
p. 160). Johnson et al. (2009, p. 3) found
that higher proportions of selfpollination occurred in smaller
populations of a moth-pollinated
orchid, Satyrium longicauda (no
common name), presumably due to
pollinators visiting more flowers per
plant in smaller populations and more
frequently transferring pollen among
flowers within a single inflorescence,
rather than frequently moving among
separate inflorescences on different
individuals. To the extent that rates of
cross-pollination, fruit set, germination,
and propagation success are lower for
white fringeless orchid populations of
small size, demographic reductions
resulting from other threats place the
species at greater risk of localized
extinctions.
While the results of genetic analyses
did not demonstrate that genetic
variability in populations of white
fringeless orchid has been eroded by
restricted gene flow, Birchenko (2001,
pp. 34–40) cautioned that interactions
between demographic and ecological
factors could be a cause for some of the
declines in white fringeless orchid
population sizes and could ultimately
cause declines in the species’ genetic
variation and increase differentiation
among its populations. The ability of
populations to adapt to environmental
change is dependent upon genetic
variation, a property of populations that
derives from its members possessing
different forms (i.e., alleles) of the same
gene (Primack 1998, p. 283). Small
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populations occurring in isolation on
the landscape can lose genetic variation
due to the potentially strong influence
of genetic drift, i.e., the random change
in allele frequency from generation to
generation (Barrett and Kohn 1991, p.
8). Smaller populations experience
greater changes in allele frequency due
to drift than do larger populations
(Allendorf and Luikart 2007, pp. 121–
122). Loss of genetic variation due to
genetic drift heightens susceptibility of
small populations to adverse genetic
effects, including inbreeding depression
and loss of evolutionary flexibility
(Primack 1998, p. 283). Deleterious
effects of loss of genetic variation
through drift have been termed drift
load, which is expressed as a decline in
mean population performance of
offspring in small populations (Willi et
al. 2005, p. 2260).
Climate Change
Our analyses under the Act include
consideration of ongoing and projected
changes in climate. The terms ‘‘climate’’
and ‘‘climate change’’ are defined by the
Intergovernmental Panel on Climate
Change (IPCC). ‘‘Climate’’ refers to the
mean and variability of different types
of weather conditions over time, with 30
years being a typical period for such
measurements, although shorter or
longer periods also may be used (IPCC
2014, pp. 119–120). 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 2014, pp. 119–120). A recent
compilation of climate change and its
effects is available from reports of the
IPCC (IPCC 2014, entire).
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). Projected
changes in climate and related impacts
can vary substantially across and within
different regions of the world (e.g., IPCC
2014, pp. 11–13). Therefore, we use
‘‘downscaled’’ projections when they
are available and have been developed
through appropriate scientific
procedures (see Glick et al. 2011, pp.
58–61, for a discussion of downscaling).
In our analyses, we use our expert
judgment to weigh relevant information,
including uncertainty, in our
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consideration of various aspects of
climate change.
The IPCC concluded that evidence of
warming of the climate system is
unequivocal (IPCC 2014, pp. 2, 40).
Numerous long-term climate changes
have been observed including changes
in arctic temperatures and ice,
widespread changes in precipitation
amounts, ocean salinity, and aspects of
extreme weather including heavy
precipitation and heat waves (IPCC
2014, pp. 40–44). While continued
change is certain, the magnitude and
rate of change is unknown in many
cases. Species that are dependent on
specialized habitat types, are limited in
distribution, or have become restricted
to the extreme periphery of their range
will be most susceptible to the impacts
of climate change.
Estimates of the effects of climate
change using available climate models
lack the geographic precision needed to
predict the magnitude of effects at a
scale small enough to discretely apply
to the range of white fringeless orchid
(i.e., there are no ‘‘downscaled’’
projections available). However, data on
recent trends and predicted changes for
the Southeast United States (Karl et al.
2009, pp. 111–122) provide some
insight for evaluating the potential
threat of climate change to the species.
White fringeless orchid’s geographic
range lies within the geographic area
included by Karl et al. (2009, pp. 111–
116) in their summary of regional
climate impacts affecting the Southeast
region.
Since 1970, the average annual
temperature across the Southeast has
increased by about 2 degrees Fahrenheit
(°F), with the greatest increases
occurring during winter months. The
geographic extent of areas in the
Southeast region affected by moderate to
severe spring and summer drought has
increased over the past three decades by
12 and 14 percent, respectively (Karl et
al. 2009, p. 111). These trends are
expected to increase. Rates of warming
are predicted to more than double in
comparison to what the Southeast has
experienced since 1975, with the
greatest increases projected for summer
months. Depending on the emissions
scenario used for modeling change,
average temperatures are expected to
increase by 4.5 °F to 9 °F by the 2080s
(Karl et al. 2009, p. 111). While there is
considerable variability in rainfall
predictions throughout the region,
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, intensity, and duration of
drought events (Karl et al. 2009, p. 112).
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Depending on timing and intensity of
drought events, white fringeless orchid
occurrences could be adversely affected
by increased mortality rates, reduced
reproductive output due to loss or
reduced vigor of mature plants, and
reduced rates of seed germination and
seedling recruitment. Further, white
fringeless orchid’s dependence upon a
limited number of large Lepidoptera for
pollination (Zettler et al. 1996, pp.16–
22) and, potentially, on a single species
of mycorrhizal fungi to complete its life
cycle (Currah et al. 1997, p. 340) place
the species at higher risk of extinction
due to environmental changes that
could diminish habitat suitability for it
or the other species upon which it
depends (Swarts and Dixon 2009, p.
546).
While climate has changed in recent
decades in the southeastern United
States and the rate of change likely will
continue to increase into the future, we
do not have data to determine
specifically how the habitats where
white fringeless orchid occurs will be
affected by, or how the species will
respond to, these changes. However, the
potential for adverse effects to white
fringeless orchid, either through
changes in habitat suitability or by
affecting populations of pollinators or
mycorrhizal fungi, is likely to increase
as climate continues to change at an
accelerating rate.
Based on our review of the best
commercial and scientific data
available, diminished resilience of many
occurrences due to small population
sizes and the species’ dependence on a
limited number of Lepidoptera and a
single species of fungi to complete its
life cycle are currently threats of
moderate magnitude to white fringeless
orchid. These threats are expected to
continue and, in light of climate change
projections, possibly increase in the
future.
Proposed Determination
We have carefully assessed the best
scientific and commercial information
available regarding the past, present,
and future threats to the white fringeless
orchid. Habitat destruction and
modification (Factor A) from
development, silvicultural practices,
excessive shading, and altered
hydrology (i.e., pond construction,
beaver dam removal) have resulted in
extirpation of the species from 10 sites.
These threats, in addition to invasive
plant species, feral hogs, and right-ofway maintenance, are associated with
habitat modifications affecting dozens of
other occurrences that are extant or of
uncertain status. Collecting for
scientific, recreational, or commercial
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purposes (Factor B) has been attributed
as the cause for extirpation of white
fringeless orchid at its type locality, and
recent evidence demonstrates that this
activity remains a threat to this species.
Fungal pathogens have been identified
as a threat to white fringeless orchid,
but a threat with potentially greater
impact associated with Factor C is
inflorescence herbivory, presumably by
deer, which has been reported at over
one-third of extant occurrences and
likely is a factor threatening most white
fringeless orchid occurrences, especially
where low numbers of plants are
present. Tuber herbivory by feral hogs
has been reported at the largest known
white fringeless orchid occurrence. The
effects of these threats are intensified by
the small population sizes that
characterize a majority of occurrences
throughout the species’ geographic
range (Factor E), due to their diminished
resilience to recover from demographic
reductions caused by loss of individuals
or low reproductive output from other
threats. Further, the species’
dependence on a limited number of
Lepidoptera and a single species of
fungi to complete its life cycle, make it
vulnerable to disturbances that diminish
habitat suitability for these taxa as well
(Factor E). Existing regulatory
mechanisms have not led to a reduction
or removal of threats posed to the
species from these factors (see Factor D
discussion).
The Act defines an endangered
species as any species that is ‘‘in danger
of extinction throughout all or a
significant portion of its range’’ and a
threatened species as any species ‘‘that
is likely to become endangered
throughout all or a significant portion of
its range within the foreseeable future.’’
We find that white fringeless orchid is
likely to become endangered throughout
all or a significant portion of its range
within the foreseeable future based on
the low to moderate threats currently
impacting the species. The species is
known to be extant at 58 locations, but
low numbers of individuals have been
observed at more than half of these (see
Figure 1, above), distributed across the
species’ range, and their persistence into
the future is uncertain. Furthermore, the
threats of habitat destruction or
modification and herbivory are present
throughout the species’ geographic
range. Left unmanaged, these threats
will likely lead to further reductions in
the species’ geographic range and
abundance at individual sites,
increasing the risk of extinction to the
point of endangerment. Therefore, on
the basis of the best available scientific
and commercial information, we
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propose listing the white fringeless
orchid as threatened in accordance with
sections 3(20) and 4(a)(1) of the Act. The
species does not currently meet the
definition of endangered, because a
sufficient number of robust populations
are present on publicly owned or
managed lands. Conservation efforts
have been initiated that could be
effective in reducing threats by
increasing population sizes and
improving habitat conditions across
much of the species’ geographic range.
Under the Act and our implementing
regulations, a species may warrant
listing if it is endangered or threatened
throughout all or a significant portion of
its range. The threats to the survival of
white fringeless orchid occur
throughout the species’ range and are
not restricted to any particular
significant portion of that range.
Accordingly, our assessment and
proposed determination applies to the
species throughout its entire range.
Therefore, because we have determined
that white fringeless orchid is
threatened throughout all of its range,
no portion of its range can be
‘‘significant’’ for purposes of the
definitions of ‘‘endangered species’’ and
‘‘threatened species.’’ See the Final
Policy on Interpretation of the Phrase
‘‘Significant Portion of Its Range’’ in the
Endangered Species Act’s Definitions of
‘‘Endangered Species’’ and ‘‘Threatened
Species’’ (79 FR 37578; July 1, 2014).
Critical Habitat and Prudency
Determination
Critical habitat is defined in section 3
of the Act as:
(1) The specific areas within the
geographic area occupied by the species,
at the time it is listed in accordance
with the Act, on which are found those
physical or biological features:
(a) Essential to the conservation of the
species, and
(b) Which may require special
management considerations or
protection; and
(2) Specific areas outside the
geographical area occupied by the
species at the time it is listed, upon a
determination that such areas are
essential for the conservation of the
species.
Conservation, as defined under
section 3 of the Act, means to use and
the use of all methods and procedures
that are necessary to bring an
endangered or threatened species to the
point at which the measures provided
pursuant to the Act are no longer
necessary.
Section 4(a)(3) of the Act, as
amended, and implementing regulations
(50 CFR 424.12), require that, to the
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maximum extent prudent and
determinable, the Secretary shall
designate critical habitat at the time the
species is determined to be an
endangered or threatened species. Our
regulations (50 CFR 424.12(a)(1)) state
that the designation of critical habitat is
not prudent when one or both of the
following situations exist:
(1) The species is threatened by
taking, collection, or other human
activity, and identification of critical
habitat can be expected to increase the
degree of threat to the species, or
(2) Such designation of critical habitat
would not be beneficial to the species.
We have determined that white
fringeless orchid is threatened by taking,
collection, or other human activity and
that identification of critical habitat
would be expected to increase this
threat. We also have determined that
little measurable benefit to the species
would result from designation of critical
habitat. This determination involves
weighing the expected increase in
threats associated with a critical habitat
designation against the benefits gained
by a critical habitat designation. An
explanation of this ‘‘balancing’’
evaluation follows.
Increased Threat to the Species by
Designating Critical Habitat
Designation of critical habitat requires
publication of maps and a narrative
description of specific critical habitat
areas in the Federal Register. The
degree of detail in those maps and
boundary descriptions is far greater than
the general location descriptions
provided in this listing proposal. Also,
while general location data (e.g., names
of administrative units of the National
Park Service (NPS), USFS, or State
conservation agencies where the species
occurs) concerning white fringeless
orchid are available, maps or detailed
descriptions are not found in scientific
or popular literature, current agency
management plans, or other readily
available sources. One exception is the
availability online of a now expired
management plan for a site in Alabama
with maps depicting two locations of
the species. Location information can
also be found in a journal article for a
site in North Carolina, where the species
is no longer extant. Designation of
critical habitat would more widely
announce the exact location of the white
fringeless orchid to poachers, collectors,
and vandals and further facilitate
unauthorized collection. Due to its
rarity (low numbers of individuals in
most populations), this orchid is highly
vulnerable to collection. Removal of
individuals from extant populations
would have devastating consequences
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in terms of reducing their viability, if
not causing outright extirpation. These
threats would be exacerbated by the
publication of maps and descriptions
outlining the specific locations of this
imperiled orchid in the Federal Register
and local newspapers. Maps and
descriptions of critical habitat, such as
those that would appear in the Federal
Register if critical habitat were
designated, are not now available to the
general public.
We have discussed evidence related
to poaching and commercial sale of
white fringeless orchid and other
congeners above (see Factor B, above).
Due to the species’ rarity, the small sizes
of most known populations, and the fact
that most of the populations are located
in remote sites that are infrequently
monitored by conservation
organizations or law enforcement,
collection is a threat to white fringeless
orchid. In small populations, the
collection of even a few individuals
would diminish reproductive output
and likely reduce genetic diversity.
Identification of critical habitat would
increase the magnitude and severity of
this threat by spatially depicting exactly
where the species may be found and
widely publicizing this information,
exposing these fragile populations and
their habitat to greater risks. We have
reviewed management plans and other
documents produced by Federal and
State conservation agencies and
scientific literature, and detailed
information on the specific locations of
white fringeless orchid sites is not
currently available.
Benefits to the Species From Critical
Habitat Designation
It is true that designation of critical
habitat for endangered or threatened
species could have some beneficial
effects. Section 7(a)(2) of the Act
requires Federal agencies, including the
Service, to ensure that actions they
fund, authorize, or carry out are not
likely to jeopardize the continued
existence of any endangered or
threatened species or result in the
destruction or adverse modification of
that species’ critical habitat. Critical
habitat only provides protections where
there is a Federal nexus, that is, those
actions that come under the purview of
section 7 of the Act. Critical habitat
designation has no application to
actions that do not have a Federal
nexus. Section 7(a)(2) of the Act
mandates that Federal agencies, in
consultation with the Service, evaluate
the effects of its proposed action on any
designated critical habitat. Similar to
the Act’s requirement that a Federal
agency action not jeopardize the
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continued existence of listed species,
Federal agencies have the responsibility
not to implement actions that would
destroy or adversely modify designated
critical habitat. Critical habitat
designation alone, however, does not
require that a Federal action agency
implement specific steps toward species
recovery.
Available data indicate that white
fringeless orchid is known from 58
extant occurrences and from 22 others
whose current status is uncertain. Of
these 80 occurrences, 17 are located on
Federal lands managed by the USFS
(12), NPS (3), and the Service (2), where
they currently receive protection from
adverse effects of management actions
and, in some cases, receive management
specifically to benefit the species and its
habitat. Management efforts have taken
place to control feral hogs and invasive
plants, increase light availability by
reducing woody vegetation cover, and
restore hydrology. In addition, the USFS
recently entered a Master Stewardship
Agreement with the Atlanta Botanical
Garden to provide for habitat
management, captive propagation, and
reintroduction or augmentation of
populations on USFS lands, where
appropriate. Some of the populations on
Federal lands are the largest known, and
any future activity involving a Federal
action that would destroy or adversely
modify critical habitat at these sites
would also likely jeopardize the species’
continued existence. Consultation with
respect to critical habitat would provide
additional protection to a species only
if the agency action would result in the
destruction or adverse modification of
the critical habitat but would not
jeopardize the continued existence of
the species. In the absence of a critical
habitat designation, areas that support
white fringeless orchid will continue to
be subject to conservation actions
implemented under section 7(a)(1) of
the Act and to the regulatory protections
afforded by the section 7(a)(2) jeopardy
standard, as appropriate.
Another possible benefit to white
fringeless orchid from designating
critical habitat would be that it could
serve to educate landowners; State and
local government agencies; visitors to
National Forests, National Parks, and
National Wildlife Refuges; and the
general public regarding the potential
conservation value of the areas.
However, through the process of
recognizing white fringeless orchid as a
candidate for Federal listing, much of
this educational benefit has already
been realized and designating critical
habitat would do little to increase
awareness about the species’ presence
and need for conservation among
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affected land managers. Agencies,
organizations, and stakeholders are
actively engaged in efforts to raise
awareness for the orchid and its
conservation needs. For example, the
Atlanta Botanical Garden received a
Five Star Urban Habitat Restoration
grant to improve habitat at several white
fringeless orchid sites in Georgia,
propagate the species for
reintroductions or augmentations, and
establish educational bog gardens at
Chattahoochee Nature Center and the
Atlanta Botanical Garden. This project,
which is separate from the USFS
agreement discussed above, involves
seven official partners, including two
local high schools and Georgia State
University. In addition, designation of
critical habitat could inform State
agencies and local governments about
areas that could be conserved under
State laws or local ordinances. However,
as awareness and education involving
white fringeless orchid is already well
underway and the species currently
receives protection from adverse effects
of management activities where it
occurs on public and privately owned
conservation lands, designation of
critical habitat would likely provide
only minimal incremental benefits.
Increased Threat to the Species
Outweighs the Benefits of Critical
Habitat Designation
Upon reviewing the available
information, we have determined that
the designation of critical habitat would
increase the threat to white fringeless
orchid from unauthorized collection
and trade. At the same time, designation
of critical habitat is likely to confer little
measurable benefit to the species
beyond that provided by listing. Overall,
the risk of increasing significant threats
to the species by publishing detailed
location information in a critical habitat
designation greatly outweighs the
benefits of designating critical habitat.
In conclusion, we find that the
designation of critical habitat is not
prudent, in accordance with 50 CFR
424.12(a)(1), because white fringeless
orchid is threatened by collection, and
designation can reasonably be expected
to increase the degree of this threat to
the species and its habitat. However, we
seek public comment on our
determination that designation of
critical habitat is not prudent.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
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Recognition through listing results in
public awareness, and conservation by
Federal, State, Tribal, and local
agencies, private organizations, and
individuals. The Act encourages
cooperation with the States and other
countries and calls for recovery actions
to be carried out for listed species. The
protection required by Federal agencies
and the prohibitions against certain
activities are discussed, in part, below.
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Subsection 4(f) of
the Act calls for the Service to develop
and implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse the species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, selfsustaining, and functioning components
of their ecosystems.
Recovery planning includes the
development of a recovery outline
shortly after a species is listed and
preparation of a draft and final recovery
plan. The recovery outline guides the
immediate implementation of urgent
recovery actions and describes the
process to be used to develop a recovery
plan. Revisions of the plan may be done
to address continuing or new threats to
the species, as new substantive
information becomes available. The
recovery plan also identifies recovery
criteria for review of when a species
may be ready for downlisting or
delisting, and methods for monitoring
recovery progress. Recovery plans also
establish a framework for agencies to
coordinate their recovery efforts and
provide estimates of the cost of
implementing recovery tasks. Recovery
teams (composed of species experts,
Federal and State agencies,
nongovernmental organizations, and
stakeholders) are often established to
develop recovery plans. If the species is
listed, the recovery outline, draft
recovery plan, and the final recovery
plan, when completed, would be
available on our Web site (https://
www.fws.gov/endangered), or from our
Tennessee Ecological Services Field
Office (see FOR FURTHER INFORMATION
CONTACT).
Implementation of recovery actions
generally requires the participation of a
broad range of partners, including other
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Federal agencies, States, Tribes,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private, State, and Tribal lands. If
this species is listed, funding for
recovery actions will be available from
a variety of sources, including Federal
budgets, State programs, and cost share
grants for non-Federal landowners, the
academic community, and
nongovernmental organizations. In
addition, pursuant to section 6 of the
Act, the State(s) of Georgia, South
Carolina, and Tennessee and the
Commonwealth of Kentucky would be
eligible for Federal funds to implement
management actions that promote the
protection or recovery of the white
fringeless orchid. Information on our
grant programs that are available to aid
species recovery can be found at:
https://www.fws.gov/grants.
Although the white fringeless orchid
is only proposed for listing under the
Act at this time, please let us know if
you are interested in participating in
conservation efforts for this species.
Additionally, we invite you to submit
any new information on this species
whenever it becomes available and any
information you may have for
conservation planning purposes (see
FOR FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as an endangered
or threatened species and with respect
to its critical habitat, if any is
designated. Regulations implementing
this interagency cooperation provision
of the Act are codified at 50 CFR part
402. Section 7(a)(4) of the Act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2) of
the Act requires Federal agencies to
ensure that activities they authorize,
fund, or carry out are not likely to
jeopardize the continued existence of
the species or destroy or adversely
modify its critical habitat. If a Federal
action may affect a listed species or its
critical habitat, the responsible Federal
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agency must enter into consultation
with the Service.
Federal agency actions within the
species’ habitat that may require
conference or consultation or both as
described in the preceding paragraph
include management and any other
landscape-altering activities on Federal
lands administered by the U.S. Fish and
Wildlife Service, USFS, and NPS;
issuance of section 404 CWA permits by
the Corps; powerline right-of-way
construction and maintenance by the
Tennessee Valley Authority; and
construction and maintenance of roads
or highways by the Federal Highway
Administration.
With respect to threatened plants, 50
CFR 17.71 provides that all of the
provisions at 50 CFR 17.61 shall apply
to threatened plants. These provisions
make it illegal for any person subject to
the jurisdiction of the United States to
import or export, transport in interstate
or foreign commerce in the course of a
commercial activity, sell or offer for sale
in interstate or foreign commerce, or to
remove and reduce to possession any
such plant species from areas under
Federal jurisdiction. In addition, the Act
prohibits malicious damage or
destruction of any such species on any
area under Federal jurisdiction, and the
removal, cutting, digging up, or
damaging or destroying of any such
species on any other area in knowing
violation of any State law or regulation,
or in the course of any violation of a
State criminal trespass law. However,
there is the following exception for
threatened plants. Seeds of cultivated
specimens of species treated as
threatened shall be exempt from all the
provisions of 50 CFR 17.61, provided
that a statement that the seeds are of
‘‘cultivated origin’’ accompanies the
seeds or their container during the
course of any activity otherwise subject
to these regulations. Exceptions to these
prohibitions are outlined in 50 CFR
17.72.
We may issue permits to carry out
otherwise prohibited activities
involving threatened plants under
certain circumstances. Regulations
governing permits are codified at 50
CFR 17.72. With regard to threatened
plants, a permit issued under this
section must be for one of the following:
Scientific purposes, the enhancement of
the propagation or survival of
threatened species, economic hardship,
botanical or horticultural exhibition,
educational purposes, or other activities
consistent with the purposes and policy
of the Act.
It is our policy, as published in the
Federal Register on July 1, 1994 (59 FR
34272), to identify to the maximum
PO 00000
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Fmt 4702
Sfmt 4702
extent practicable at the time a species
is listed, those activities that would or
would not constitute a violation of
section 9 of the Act. The intent of this
policy is to increase public awareness of
the effect of a proposed listing on
proposed and ongoing activities within
the range of species proposed for listing.
Based on the best available
information, the following activities
may potentially result in a violation of
section 9 the Act; this list is not
comprehensive:
(1) Unauthorized collecting, handling,
possessing, selling, delivering, carrying,
or transporting of white fringeless
orchid, including import or export
across State lines and international
boundaries, except for properly
documented antique specimens of this
species at least 100 years old, as defined
by section 10(h)(1) of the Act;
(2) Unauthorized removal, damage, or
destruction of white fringeless orchid
plants from populations located on
Federal land (USFS, NPS, and Service
lands); and
(3) Unauthorized removal, damage, or
destruction of white fringeless orchid
plants on private land in violation of
any State regulation, including criminal
trespass.
At this time, we are unable to identify
specific activities that would not be
considered to result in a violation of
section 9 of the Act because white
fringeless orchid occurs in a variety of
habitat conditions across its range and
it is likely that site-specific conservation
measures may be needed for activities
that may directly or indirectly affect the
species.
Questions regarding whether specific
activities would constitute a violation of
section 9 of the Act should be directed
to the Tennessee Ecological Services
Field Office (see FOR FURTHER
INFORMATION CONTACT).
Required Determinations
Clarity of the Rule
We are required by Executive Orders
12866 and 12988 and by the
Presidential Memorandum of June 1,
1998, to write all rules in plain
language. This means that each rule we
publish must:
(1) Be logically organized;
(2) Use the active voice to address
readers directly;
(3) Use clear language rather than
jargon;
(4) Be divided into short sections and
sentences; and
(5) Use lists and tables wherever
possible.
If you feel that we have not met these
requirements, send us comments by one
E:\FR\FM\15SEP1.SGM
15SEP1
55321
Federal Register / Vol. 80, No. 178 / Tuesday, September 15, 2015 / Proposed Rules
of the methods listed in the ADDRESSES
section. To better help us revise the
rule, your comments should be as
specific as possible. For example, you
should tell us the numbers of the
sections or paragraphs that are unclearly
written, which sections or sentences are
too long, the sections where you feel
lists or tables would be useful, etc.
National Environmental Policy Act
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act
(NEPA; 42 U.S.C. 4321 et seq.), need not
be prepared in connection with listing
a species as an endangered or
threatened species under the
Endangered Species Act. We published
a notice outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
References Cited
A complete list of references cited in
this rulemaking is available on the
Internet at https://www.regulations.gov
and upon request from the Tennessee
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Authors
The primary authors of this proposed
rule are the staff members of the
Tennessee Ecological Services Field
Office.
List of Subjects in 50 CFR Part 17
50 of the Code of Federal Regulations,
as set forth below:
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.
2. In § 17.12(h), add an entry for
Platanthera integrilabia (white
fringeless orchid) to the List of
Endangered and Threatened Plants in
alphabetical order under FLOWERING
PLANTS to read as follows:
■
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
§ 17.12
Proposed Regulation Promulgation
*
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
Endangered and threatened plants.
*
*
(h) * * *
*
Species
Historic range
Scientific name
Family
Status
When listed
Common name
*
Critical
habitat
Special
rules
FLOWERING PLANTS
*
Platanthera
integrilabia.
*
White fringeless orchid.
*
*
*
*
*
*
*
U.S.A. (AL, GA, KY,
MS, NC, SC, TN).
*
Orchidaceae ...........
*
*
*
T
*
....................
*
*
Dated: August 14, 2015.
Stephen Guertin,
Director, U.S. Fish and Wildlife Service.
*
[FR Doc. 2015–22973 Filed 9–14–15; 8:45 am]
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Agencies
[Federal Register Volume 80, Number 178 (Tuesday, September 15, 2015)]
[Proposed Rules]
[Pages 55304-55321]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-22973]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R4-ES-2015-0129; 4500030113]
RIN 1018-BA93
Endangered and Threatened Wildlife and Plants; Threatened Species
Status for Platanthera integrilabia (White Fringeless Orchid)
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), propose to
list Platanthera integrilabia (white fringeless orchid), a plant
species from Alabama, Georgia, Kentucky, Mississippi, South Carolina,
and Tennessee, as a threatened species under the Endangered Species Act
(Act). If we finalize this rule as proposed, it
[[Page 55305]]
would extend the Act's protections to this species.
DATES: We will accept comments received or postmarked on or before
November 16, 2015. Comments submitted electronically using the Federal
eRulemaking Portal (see ADDRESSES) must be received by 11:59 p.m.
Eastern Time on the closing date. We must receive requests for public
hearings, in writing, at the address shown in FOR FURTHER INFORMATION
CONTACT by October 30, 2015.
ADDRESSES: You may submit comments by one of the following methods:
(1) Electronically: Go to the Federal eRulemaking Portal: https://www.regulations.gov. In the Search box, enter FWS-R4-ES-2015-0129,
which is the docket number for this rulemaking. Then, in the Search
panel on the left side of the screen, under the Document Type heading,
click on the Proposed Rules link to locate this document. You may
submit a comment by clicking on ``Comment Now!''
(2) By hard copy: Submit by U.S. mail or hand-delivery to: Public
Comments Processing, Attn: FWS-R4-ES-2015-0129; U.S. Fish and Wildlife
Service, MS: BPHC, 5275 Leesburg Pike, Falls Church, VA 22041-3803.
We request that you send comments only by the methods described
above. We will post all comments on https://www.regulations.gov. This
generally means that we will post any personal information you provide
us (see Public Comments, below, for more information).
FOR FURTHER INFORMATION CONTACT: Mary Jennings, Field Supervisor, U.S.
Fish and Wildlife Service, Tennessee Ecological Services Field Office,
446 Neal Street, Cookeville, TN 38501; by telephone 931-528-6481; or by
facsimile 931-528-7075. Persons who use a telecommunications device for
the deaf (TDD) may call the Federal Information Relay Service (FIRS) at
800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. Under the Act, if we determine that
a species is an endangered or threatened species throughout all or a
significant portion of its range, we are required to promptly publish a
proposal in the Federal Register and make a determination on our
proposal within 1 year. Listing a species as an endangered or
threatened species and designations and revisions of critical habitat
can only be completed by issuing a rule.
This rule proposes the listing of Platanthera integrilabia (white
fringeless orchid) as a threatened species. The white fringeless orchid
is a candidate species for which we have on file sufficient information
on biological vulnerability and threats to support preparation of a
listing proposal, but for which development of a listing regulation has
been precluded by other higher priority listing activities. This rule
reassesses all available information regarding status of and threats to
the white fringeless orchid.
This rule does not propose critical habitat for white fringeless
orchid. We have determined that designation of critical habitat would
not be prudent for this species because:
Designation would increase the likelihood and severity of
illegal collection of white fringeless orchid and thereby make
enforcement of take prohibitions more difficult.
This threat outweighs the benefits of designation.
The basis for our action. Under the Act, we may determine that a
species is an endangered or threatened species based on any of five
factors: (A) The present or threatened destruction, modification, or
curtailment of its habitat or range; (B) overutilization for
commercial, recreational, scientific, or educational purposes; (C)
disease or predation; (D) the inadequacy of existing regulatory
mechanisms; or (E) other natural or manmade factors affecting its
continued existence. We have determined that the threats to white
fringeless orchid consist primarily of destruction and modification of
habitat (Factor A) resulting in excessive shading, soil disturbance,
altered hydrology, and proliferation of invasive plant species;
collecting for recreational or commercial purposes (Factor B);
herbivory (Factor C); and small population sizes and dependence on
specific pollinators and fungi to complete its life cycle (Factor E).
Existing regulatory mechanisms have not led to a reduction or removal
of threats posed to the species from these factors (see Factor D
discussion).
We will seek peer review. We will seek comments from independent
specialists to ensure that our designation is based on scientifically
sound data, assumptions, and analyses. We will invite these peer
reviewers to comment on our listing proposal.
Information Requested
Public Comments
We intend that any final action resulting from this proposed rule
will be based on the best scientific and commercial data available and
be as accurate and as effective as possible. Therefore, we request
comments or information from other concerned governmental agencies,
Native American tribes, the scientific community, industry, or any
other interested parties concerning this proposed rule. We particularly
seek comments concerning:
(1) The white fringeless orchid's biology, range, and population
trends, including:
(a) Biological or ecological requirements of the species, including
habitat requirements for germination, growth, and reproduction;
(b) Genetics and taxonomy;
(c) Historical and current range, including distribution patterns;
(d) Historical and current population levels, and current and
projected trends; and
(e) Past and ongoing conservation measures for the species, its
habitat, or both.
(2) Factors that may affect the continued existence of the species,
which may include habitat modification or destruction, overutilization,
disease, predation, the inadequacy of existing regulatory mechanisms,
or other natural or manmade factors.
(3) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to this species and existing regulations
that may be addressing those threats.
(4) The reasons why we should or should not designate habitat as
``critical habitat'' under section 4 of the Act (16 U.S.C. 1531 et
seq.), including whether there are threats to the species from human
activity, the degree of which can be expected to increase due to the
designation, and whether that increase in threat outweighs the benefit
of designation such that the designation of critical habitat is not
prudent.
Please include sufficient information with your submission (such as
scientific journal articles or other publications) to allow us to
verify any scientific or commercial information you include.
Please note that submissions merely stating support for or
opposition to the action under consideration without providing
supporting information, although noted, will not be considered in
making a determination, as section 4(b)(1)(A) of the Act directs that
determinations as to whether any species is an endangered or threatened
species must be made ``solely on the basis of the best scientific and
commercial data available.''
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in the ADDRESSES section. We request
that you
[[Page 55306]]
send comments only by the methods described in the ADDRESSES section.
If you submit information via https://www.regulations.gov, your
entire submission--including any personal identifying information--will
be posted on the Web site. If your submission is made via a hardcopy
that includes personal identifying information, you may request at the
top of your document that we withhold this information from public
review. However, we cannot guarantee that we will be able to do so. We
will post all hardcopy submissions on https://www.regulations.gov.
Comments and materials we receive, as well as supporting
documentation we used in preparing this proposed rule, will be
available for public inspection on https://www.regulations.gov, or by
appointment, during normal business hours, at the U.S. Fish and
Wildlife Service, Tennessee Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Because we will consider all comments and information received
during the public comment period, our final determinations may differ
from this proposal.
Public Hearing
Section 4(b)(5) of the Act provides for one or more public hearings
on this proposal, if requested. Requests must be received within 45
days after the date of publication of this proposed rule in the Federal
Register. Such requests must be sent to the address shown in the FOR
FURTHER INFORMATION CONTACT section. We will schedule public hearings
on this proposal, if any are requested, and announce the dates, times,
and places of those hearings, as well as how to obtain reasonable
accommodations, in the Federal Register and local newspapers at least
15 days before the hearing.
Peer Review
In accordance with our joint policy on peer review published in the
Federal Register on July 1, 1994 (59 FR 34270), we will seek the expert
opinions of at least three appropriate and independent specialists
regarding this proposed rule. The purpose of peer review is to ensure
that our listing determination is based on scientifically sound data,
assumptions, and analyses. The peer reviewers have expertise with the
white fringeless orchid's biology, habitat, physical or biological
factors, distribution, and status, or have general botanical and
conservation biology expertise.
Previous Federal Action
The Act requires the Service to identify species of wildlife and
plants that are endangered or threatened, based on the best available
scientific and commercial data. Section 12 of the Act directed the
Secretary of the Smithsonian Institution to prepare a report on
endangered and threatened plant species, which was published as House
Document No. 94-51. The Service published a notice in the Federal
Register on July 1, 1975 (40 FR 27824), in which we announced that more
than 3,000 native plant taxa named in the Smithsonian's report and
other taxa added by the 1975 notice would be reviewed for possible
inclusion in the List of Endangered and Threatened Plants. The 1975
notice was superseded on December 15, 1980 (45 FR 82480), by a new
comprehensive notice of review for native plants that took into account
the earlier Smithsonian report and other accumulated information. On
November 28, 1983 (48 FR 53640), a supplemental plant notice of review
noted the status of various taxa. Complete updates of the plant notice
were published on September 27, 1985 (50 FR 39526), February 21, 1990
(55 FR 6184), and September 30, 1993 (58 FR 51144).
White fringeless orchid was first listed as a Category 1 candidate
in the December 15, 1980, review. Category 1 candidates included taxa
for which the Service had sufficient information on hand to support the
biological appropriateness of listing as endangered or threatened
species. The species was reclassified as a Category 2 candidate in the
November 28, 1983, review. Category 2 candidates included taxa for
which the Service had information indicating that proposing to list the
species as endangered or threatened was possibly appropriate, but for
which sufficient data on biological vulnerability and threat were not
available. Further biological research and field study usually was
necessary to ascertain the status of taxa in this category.
In 1996, the Service eliminated candidate categories (February 28,
1996; 61 FR 7596), and white fringeless orchid was no longer a
candidate until it was again elevated to candidate status on October
25, 1999 (64 FR 57534). The species was also included in subsequent
candidate notices of review on October 30, 2001 (66 FR 54808), June 13,
2002 (67 FR 40657), May 4, 2004 (69 FR 24876), May 11, 2005 (70 FR
24870), September 12, 2006 (71 FR 53756), December 6, 2007 (72 FR
69034), December 10, 2008 (73 FR 75176), November 9, 2009 (74 FR
57804), November 10, 2010 (75 FR 69222), October 26, 2011 (76 FR
66370), November 21, 2012 (77 FR 69994), November 22, 2013 (78 FR
70104), and December 5, 2014 (79 FR 72450).
The 2011 Multi-District Litigation (MDL) settlement agreement
specified that the Service will systematically, over a period of 6
years, review and address the needs of 251 candidate species to
determine if they should be added to the Federal Lists of Endangered
and Threatened Wildlife and Plants. The white fringeless orchid was on
that list of candidate species. Therefore, the Service is making this
proposed listing determination in order to comply with the conditions
outlined in the MDL agreement.
Background
Species Information
Taxonomy and Species Description
White fringeless orchid was first recognized as a distinct taxon
when D.S. Correll (1941, pp. 153-157) described it as a variety of
Habenaria (Platanthera) blephariglottis. C.A. Luer (1975, p. 186)
elevated the taxon to full species status. The currently accepted
binomial for the species is Platanthera integrilabia (Correll) Luer.
The description of this taxon at the full species level used the common
name of ``monkey-face'' (Luer 1975, p. 186), as have some other
publications (Zettler and Fairey 1990, p. 212; Zettler 1994, p. 686;
Birchenko 2001, p. 9). A status survey report for the species
recognized both ``white fringeless orchid'' and ``monkeyface'' as
common names (Shea 1992, p. 1). The Service used the common name
``white fringeless orchid'' when the species was first recognized as a
candidate for listing, and we retain usage of this common name here.
White fringeless orchid is a perennial herb with a light green, 60-
centimeters (cm) (23-inches (in)) long stem that arises from a tuber
(modified underground stem of a plant that is enlarged for nutrient
storage). The leaves are alternate with entire margins and are narrowly
elliptic to lanceolate (broadest below the middle and tapering toward
the apex) in shape. The lower leaves are 20 cm (8 in) long and 3 cm (1
in) wide. The upper stem leaves are much smaller. The white flowers are
borne in a loose cluster at the end of the stem. The upper two flower
petals are about 7 millimeters (mm) (0.3 in) long, and the lower petal
(the lip) is about 13 mm (0.5 in) long. The epithet ``integrilabia''
refers to the lack of any prominent fringe on the margin of the lip
petal (Luer 1975, p. 186). The plants flower from late July through
September, and the small narrow fruiting capsule matures in October
(Shea 1992, p. 23).
[[Page 55307]]
Distribution
To determine the current distribution of white fringeless orchid,
we used data provided by Natural Heritage Programs (NHP), housed in
State agencies or universities in each of the States in the species'
geographic range: Alabama Natural Heritage Program at Auburn University
(ANHP 2014); Georgia Department of Natural Resources (GDNR 2014);
Kentucky State Nature Preserves Commission (KSNPC 2014); Mississippi
Department of Wildlife, Fisheries, and Parks (MDWFP 2014); North
Carolina Department of Environment and Natural Resources (NCDENR 2014);
South Carolina Department of Natural Resources (SCDNR 2012); and
Tennessee Department of Environment and Conservation (TDEC 2014). In
addition to NHP data, we used Shea's (1992, entire) Status Survey
Report on Platanthera integrilabia to determine the species' historical
distribution.
In most cases, a mapped occurrence in the databases maintained by
the NHPs represented a single group of plants growing together in a
patch of suitable habitat. However, the Kentucky NHP combined multiple
groups of plants (i.e., sub-occurrences), growing in distinct habitat
patches in close proximity to one another, into single occurrences. In
two instances, the Tennessee NHP also grouped several sub-occurrences
into a single occurrence, where they were all located in separate
stream heads draining into a single headwater stream. In describing the
current range and distribution of white fringeless orchid, we have
adopted these groupings in those instances where all of the sub-
occurrences were located within the drainage of a single headwater
stream. In two instances, where Kentucky NHP grouped sub-occurrences
from drainages of separate headwater streams into a single occurrence,
we split the sub-occurrences into two separate occurrences by grouping
together only those that were located within a single headwater
drainage.
Historical Distribution--As of 1991, there were 30 extant
occurrences and 13 with uncertain status, distributed among 20 counties
in 5 southeastern States (see Table 1, below). Shea (1992, pp. 14-17)
also reported on six locations with historical occurrences and six from
which the species had been extirpated.
As of 2015, there are records for 13 historical and 12 extirpated
occurrences in NHP databases. Accounting for two locations that Shea
(1992, pp. 11-14) reported as extirpated and a third reported as
uncertain but now considered to be historical, none of which is
included in NHP databases, there are 28 occurrences that currently are
considered historical or extirpated. In 1991, five of these were extant
and the status of five was uncertain (Shea 1992, pp. 7-14). Based on
these data, the species' historical range included Cobb County,
Georgia; Henderson County, North Carolina; and Roane County, Tennessee,
in addition to the 35 counties listed below in Table 1 for the species'
range as of 2014. The species has been extirpated completely from North
Carolina.
Shea (1992, pp. 17-18) lists additional records from Butler County,
Alabama; Cherokee County, North Carolina; Hamilton County, Tennessee;
and Lee County, Virginia, whose validity she could neither verify nor
refute based on available data. Lacking sufficient data to document the
collection of white fringeless orchid from Lee County, the authors of
the Flora of Virginia did not include the species (Townsend 2012, pers.
comm.). Lacking any substantive data for white fringeless orchid's
historical presence in the other three counties above, we also consider
them to not be part of the species' historical range.
Current Distribution--Using available data, we categorized the
current status of each occurrence as extant, extirpated, historical, or
uncertain. Extant occurrences are those for which recent (i.e., since
ca. 2000) observations of flowering plants are available to confirm the
species' persistence at a given site, or from which material was
collected and cultivated in a greenhouse to produce flowering specimens
confirming the identification of vegetative plants that were observed
in the field. Because white fringeless orchid commonly occurs with
three congeners (species belonging to the same genus) that share
similar leaf characteristics, conclusive identification in the absence
of flowering specimens is not possible. Extirpated occurrences are
those where the species' absence is considered to be certain due to
lack of recent observations of flowering white fringeless orchids, or
vegetative plants of any species of Platanthera, associated with
modification of the habitat to an unsuitable condition for white
fringeless orchid. White fringeless orchid was last seen flowering at
one extirpated occurrence as recently as 2004, but habitat in this
former transmission line right-of-way is no longer maintained and has
become unsuitable due to woody vegetation encroachment. Similarly,
recent observation of flowering white fringeless orchids or vegetative
plants of any species of Platanthera is lacking for historical
occurrences, but the habitat has not been visibly altered at these
locations. We have assigned uncertain status to occurrences where
recent observation of flowering white fringeless orchids is lacking,
but where basal leaves of non-flowering Platanthera spp. orchids
typically have been observed during one or more recent visits. In
addition, we have assigned uncertain status to one Mississippi
occurrence, where a single white fringeless orchid was seen flowering
in 2011, because the hydrology at this site was subsequently altered by
a drainage ditch and the species' persistence at this site is now
questionable.
The white fringeless orchid's distribution is concentrated in the
Cumberland Plateau section of the Appalachian Plateaus physiographic
province, with isolated populations scattered across the Blue Ridge,
Piedmont, and Coastal Plain provinces (Fenneman 1938, pp. 68, 134-137,
172, 333-334). The species is currently extant at 58 occurrences
distributed among 32 counties, spanning 5 southeastern States (Table
1). There are an additional 22 occurrences (Table 1) whose current
status is uncertain, which include one additional State and three
additional counties. We consider the species' current distribution to
include the 6 States and 35 counties where NHP database records for
these extant and uncertain occurrences exist (Table 1). We included
records of uncertain status in defining the species' current
distribution to ensure that all relevant State and local governments
and private stakeholders are aware of white fringeless orchid's
potential presence and opportunities for conserving the species and its
habitat.
[[Page 55308]]
Table 1--County-Level Distribution of Extant and Uncertain Status White Fringeless Orchid Occurrences, Circa
1991 (Shea 1992) and 2014 (ANHP 2014, GDNR 2014, KSNPC 2014, MDWFP 2014, NCDENR 2014, SCDNR 2012, TDEC 2014)
----------------------------------------------------------------------------------------------------------------
1991 2014
State County ---------------------------------------------------
Extant Uncertain Extant Uncertain
----------------------------------------------------------------------------------------------------------------
Alabama............................. Calhoun............... ........... ........... 2 ...........
Clay.................. ........... 1 1 ...........
Cleburne.............. ........... ........... 1 ...........
DeKalb................ ........... ........... 1 ...........
Jackson............... ........... ........... ........... 1
Marion................ 1 ........... 1 2
Tuscaloosa............ 1 ........... 1 ...........
Winston............... 1 ........... 1 ...........
Georgia............................. Bartow................ ........... ........... 1 ...........
Carroll............... 2 ........... 2 ...........
Chatooga.............. ........... ........... 1 ...........
Cobb.................. 1 ........... ........... ...........
Coweta................ 1 ........... 1 ...........
Forsyth............... ........... 1 1 ...........
Pickens............... ........... ........... 1 ...........
Rabun................. 1 ........... 1 ...........
Stephens.............. 1 ........... 1 ...........
Kentucky............................ Laurel................ ........... ........... 2 2
McCreary.............. 4 ........... 2 1
Pulaski............... 1 1 2 ...........
Whitley............... ........... ........... 1 ...........
Mississippi......................... Alcorn................ ........... ........... ........... 1
Itawamba.............. ........... ........... 2 1
Tishomingo............ ........... ........... 1 1
South Carolina...................... Greenville............ 1 ........... ........... 1
Tennessee........................... Bledsoe............... ........... 2 2 1
Cumberland............ ........... ........... 1 ...........
Fentress.............. ........... ........... 2 ...........
Franklin.............. 3 2 5 5
Grundy................ 5 5 4 4
Marion................ 2 ........... 8 ...........
McMinn................ 1 ........... 1 ...........
Polk.................. ........... ........... 1 ...........
Scott................. ........... ........... 1 ...........
Sequatchie............ 2 1 1 1
Van Buren............. 2 ........... 5 1
---------------------------------------------------
Total........................... ...................... 30 13 58 22
----------------------------------------------------------------------------------------------------------------
More occurrences are included in the species' current distribution
than were historically known to exist, likely as a result of increased
survey effort having been devoted to white fringeless orchid due to its
status as a candidate for Federal listing. However, low numbers of
flowering plants have been observed at most sites (Figure 1). For
example, fewer than 50 flowering plants have ever been observed at one
time at 45 (64 percent) of the 70 extant and uncertain occurrences for
which data are available. At 26 (37 percent) of these occurrences,
fewer than 10 flowering plants have ever been recorded.
[[Page 55309]]
[GRAPHIC] [TIFF OMITTED] TP15SE15.001
There are 32 extant occurrences that are located entirely, or in
part, on lands owned or managed by local, State, or Federal government
entities (Table 2). In addition, there are seven uncertain, five
extirpated, and two historical occurrences that are similarly situated.
Two additional occurrences, one extant and one uncertain, are located
on private lands that are protected by conservation easements.
Table 2--Status and Number of White Fringeless Orchid Occurrences on Publicly Owned or Managed Lands
[Note: One site is on privately owned lands that GDNR leases for use as a wildlife management area]
----------------------------------------------------------------------------------------------------------------
Ownership Extant Uncertain Extirpated Historical
----------------------------------------------------------------------------------------------------------------
National Park Service....................................... 3 ........... ........... ...........
U.S. Forest Service......................................... 9 3 3 ...........
U.S. Fish and Wildlife Service.............................. 2 ........... ........... ...........
Alabama Department of Conservation and Natural Resources.... ........... 1 ........... ...........
Georgia Department of Natural Resources..................... 2 ........... ........... ...........
Kentucky State Nature Preserves Commission.................. 1 ........... ........... 1
Mississippi Department of Fish, Wildlife, and Parks......... 1 ........... ........... ...........
North Carolina Plant Conservation Program................... ........... ........... 1 ...........
South Carolina State Parks.................................. ........... 1 ........... ...........
Tennessee Department of Transportation...................... 1 ........... ........... ...........
Tennessee Division of Forestry.............................. 7 ........... ........... ...........
Tennessee State Parks....................................... 5 1 ........... 1
Tennessee Wildlife Resources Agency......................... 1 ........... 1 ...........
Forsyth County, Georgia..................................... ........... 1 ........... ...........
---------------------------------------------------
Total................................................... 31 8 5 2
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Habitat
In Correll's (1941, pp. 156-157) description of white fringeless
orchid as a distinct variety, he included notes from herbarium
specimens that describe the species' habitat variously as ``bog,''
``boggy sphagnum ravine,'' ``sphagnum bog,'' ``grassy swamps,'' and
``marshy ground.'' Luer (1975, p. 186) described the habitat as ``. . .
the deep shade of damp deciduous forests . . . in the thick leaf litter
and sphagnum moss along shallow wet ravines and depressions.'' Zettler
and Fairey (1990, p. 212) observed the species growing in ``shaded and
level bogs, swamps or seepage slopes usually containing Sphagnum.''
Shea (1992, p. 19) described the habitat as ``wet, flat, boggy areas at
the head of streams or on seepage slopes . . . with Sphagnum . . .
usually grows in partial shade.''
Hoy (2012, p. 53) demonstrated that precipitation was the primary
hydrologic source for three wetlands at a white fringeless orchid site
on the Cumberland Plateau in Kentucky, which was commonly referred to
as a seep. Thus, describing many of the sites where white fringeless
orchid occurs as ``seeps'' or ``seepage slopes'' may contradict the
typical characterization of seeps as wetlands where water from
subsurface sources emerges at the surface (Soulsby et al. 2007, p.
200). The term ``bogs'' refers to a specific wetland type that
accumulates peat, lacks significant inflow or outflow, and harbors
mosses adapted to acidic environments, particularly Sphagnum (Mitsch
and Gosselink 2000, p. 41). Peat is fibric organic soil material,
meaning that some plant forms incorporated into the soil are
identifiable (U.S. Department of Agriculture, Natural Resources
Conservation Service 2006, p. 32). However, despite the common usage of
the terms ``bog'' or ``boggy'' to describe them and the nearly
ubiquitous presence of Sphagnum spp. (sphagnum moss) in them, the
wetlands that white fringeless orchid inhabits occur on mineral soils
and do not accumulate peat. Further, they often are located at stream
heads and connected to ephemeral streams via dispersed sheet flow or
concentrated surface flow in incipient channels.
Weakley and Schafale (1994, pp. 164-165) commented on the
discrepancy between regional use of the terms ``bogs'' and ``fens'' to
describe non-
[[Page 55310]]
alluvial wetlands of the Southern Blue Ridge in which sphagnum moss is
prominently featured and their more traditional usage in peatland
classifications. Noting that most of the region's non-alluvial wetlands
lacked organic soils, these authors nonetheless chose to maintain the
regional usage of these terms in their classification, to emphasize
differences in sources of hydrology and their effects on water
chemistry (nutrient-poor precipitation in ``bogs'' versus mineral-rich
groundwater seepage in ``fens''). Similar to the non-alluvial wetlands
of the Southern Blue Ridge, further study is needed to characterize the
range of variation in soils, hydrology, physicochemistry, and origin of
wetlands throughout the range of white fringeless orchid.
Most sites where white fringeless populations exist are on soils
formed over sandstone bedrock, which usually are low in fertility and
organic matter content and are acidic (Shea 1992, p. 20). The species
often occurs in swamps dominated by Acer rubrum (red maple) and Nyssa
sylvatica (blackgum), where common shrubs and woody vines include Alnus
serrulata (smooth alder), Decumaria barbara (climbing hydrangea),
Smilax spp. (greenbrier), and Viburnum nudum (possumhaw). Common
herbaceous associates of white fringeless orchid include Doellingeria
umbellata (parasol flat-top white aster), Gymnadeniopsis clavellata
(green woodland orchid), Lobelia cardinalis (cardinal flower), Lycopus
virginicus (Virginia bugleweed), Osmunda cinnamomea (cinnamon fern), O.
regalis (royal fern), Oxypolis rigidior (stiff cowbane), Parnassia
asarifolia (kidneyleaf grass of parnassus), Platanthera ciliaris
(yellow fringed orchid), P. cristata (crested yellow orchid), Sphagnum
spp. (sphagnum moss), Thelypteris noveboracensis (New York fern), Viola
primulifolia (primrose-leaf stemless white violet), and Woodwardia
areolata (chainfern) (Zettler and Fairey 1990, p. 213; Shea 1992, p.
22; Patrick 2012, pers. comm.). Sites located in powerline rights-of-
way share many of the herbaceous taxa listed above, but lack a canopy
or well-developed shrub stratum due to vegetation management.
Nomenclature follows the Integrated Taxonomic Information System
(retrieved on January 16, 2015, from the Integrated Taxonomic
Information System online database, https://www.itis.gov).
Biology
Orchid seeds are dust-like and lack an endosperm (the tissue
produced inside seeds of most flowering plants that provides nutrient
reserves) making them dependent upon acquiring carbon from an external
source (Yoder et al. 2010, p. 7). Like most terrestrial orchids, white
fringeless orchid depends on a symbiotic (interdependent) relationship
with mycorrhizal fungi (an association of a fungus and a plant in which
the fungus lives within or on the outside of the plant's roots) to
enhance seed germination and promote seedling development and
establishment (Zettler and McInnis 1992, pp. 157-160; Rasmussen and
Whigham 1993, p. 1374). In addition to providing a carbon source for
seedling development, mycorrhizal fungi enhance germination by
promoting increased water uptake by orchid seeds (Yoder et al. 2000,
149). Their small size permits dispersal of orchid seeds to new
environments via wind currents; however, very few of the seeds likely
encounter suitable habitats where host fungi are present (Yoder et al.
2010, pp. 14-16). This likelihood is further reduced in the case of
species such as white fringeless orchid, which may rely on a single
fungal host species, Epulorhiza inquilina, to complete its life cycle
(Currah et al. 1997, p. 340).
White fringeless orchid has a self-compatible breeding system,
allowing individuals to produce seed using their own pollen; however,
the proportions of fruits produced through self-pollination versus
cross-pollination are not known (Zettler and Fairey 1990, p. 214).
Rates of fruit set, measured as the proportion of individual flowers
that produced capsules, varied in studies of populations in Georgia
(6.9 percent), South Carolina (20.3 percent) (Zettler and Fairey 1990,
p. 214), and Tennessee (56.9 percent) (Zettler et al. 1996, p. 20).
While these observations were made at these populations in different
years, the Tennessee population, where pollination was observed, is
considerably larger than the Georgia or South Carolina populations,
where no pollination was observed. Zettler et al. (1996, p. 22)
reasoned that inbreeding depression was a likely cause for the lower
fruit set in the smaller populations, noting that in a separate study
both germination rates and propagation success were greater in white
fringeless orchid seeds collected from the largest of these populations
(Zettler and McInnis 1992, p. 160). They speculated that higher rates
of fruit set were probably more typical historically, when larger
populations provided greater opportunities for cross-pollination to
occur.
White fringeless orchid is capable of prodigious seed production,
which might help to compensate for the likely dispersal of many seeds
into unsuitable habitats. In the Tennessee population studied by
Zettler et al. (1996, p. 20), more than half of the flowers on
inflorescences (the complete flower head of a plant including stems,
stalks, bracts, and flowers) set fruit, resulting in a mean of 4.7
capsules per plant. The capsules produced an average of 3,433 seeds
each, indicating that each inflorescence averaged over 16,000 seeds.
With 577 inflorescences counted in the study area, Zettler et al.
(1996, p. 20) estimated that over 9,000,000 seeds were produced.
However, in separate studies of in vitro and in situ seedling
development, even with fungal inoculation less than 3 percent of seeds
developed into protocorms (young seedlings) that could be established
on soil (Zettler and McInnis 1992, pp. 157-160; Zettler 1994, pp. 65).
Known pollinators for white fringeless orchid include three diurnal
species from two families of butterflies (Lepidoptera): Silver spotted
skipper (Hesperiidae: Epargyreus clarus), spicebush swallowtail
(Papilionidae: Papilio troilus), and eastern tiger swallowtail
(Papilionidae: P. glaucus) (Zettler et al. 1996, p. 16). Based on
floral characteristics, including white flowers and a long nectiferous
(nectar bearing) spur, as well as pollinaria morphology in relation to
potential pollinator morphology, it is likely that more effective
pollinators for white fringeless orchid exist in the nocturnal sphingid
moth family (Lepidoptera: Sphingidae) (Zettler et al. 1996, pp. 17-18);
however, this has not been confirmed. Pollinaria are the pollen-bearing
structure on orchids, consisting of pollen masses (pollinia) attached
to a stalk that has a sticky pad (viscidium), which attaches the
pollinaria to pollinators (Argue 2012, p. 5). Despite the fact that
nectar concentrations in white fringeless orchid flowers did not
fluctuate significantly over a 24-hour observation period, Zettler et
al. (1996, p. 20) noticed the floral fragrance produced by a large
Tennessee population intensified between the hours of 7:00 p.m. and
11:00 p.m., suggesting the species possesses adaptions for attracting
nocturnal pollinators.
Genetics
Birchenko (2001, pp. 18-23, 47-48) analyzed genetic structure among
25 white fringeless orchid populations, distributed across Alabama,
Georgia, Tennessee, and Kentucky. Her ``populations'' corresponded to
specific NHP occurrences. The majority (79 percent) of the genetic
variation was present as variation within populations, while 21 percent
of the variation was
[[Page 55311]]
attributable to differences between populations (Birchenko 2001, p.
29). While these results alone do not demonstrate that genetic
variability in white fringeless orchid populations has been eroded by
restricted gene flow, Birchenko (2001, pp. 34-40) cautioned that
interactions between demographic and ecological factors could be a
cause for some observed population declines and could ultimately cause
declines in the species' genetic variation and increase differentiation
among white fringeless orchid populations.
Summary of Factors Affecting the Species
Under section 4(a)(1) of the Act, we may list a species based on:
(A) The present or threatened destruction, modification, or curtailment
of its habitat or range; (B) overutilization for commercial,
recreational, scientific, or educational purposes; (C) disease or
predation; (D) the inadequacy of existing regulatory mechanisms; or (E)
other natural or manmade factors affecting its continued existence.
Listing actions may be warranted based on any of the above threat
factors, singly or in combination.
Information pertaining to white fringeless orchid in relation to
the five factors provided in section 4(a)(1) of the Act is discussed
below. In considering what factors might constitute threats, we must
look beyond the mere exposure of the species to the factor to determine
whether the species responds to the factor in a way that causes actual
impacts to the species. If there is exposure to a factor, but no
response, or only a positive response, that factor is not a threat. If
there is exposure and the species responds negatively, the factor may
be a threat, and we then attempt to determine if that factor rises to
the level of a threat, meaning that it may drive or contribute to the
risk of extinction of the species such that the species warrants
listing as an endangered or threatened as those terms are defined by
the Act. This does not necessarily require empirical proof of a threat.
The combination of exposure and some corroborating evidence of how the
species is likely impacted could suffice. The mere identification of
factors that could impact a species negatively is not sufficient to
compel a finding that listing is appropriate; we require evidence that
these factors are operative threats that act on the species to the
point that the species meets the definition of an endangered or
threatened species under the Act.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
Habitat modification caused by development, silvicultural
practices, invasive plant species, disturbance by feral hogs, shading
due to understory and canopy closure, altered hydrology, and right-of-
way maintenance have impacted the range and abundance of white
fringeless orchid.
Development
One white fringeless orchid occurrence was extirpated from a site
in Henderson County, North Carolina, which Shea (1992, p. 15) reported
had been nearly completely destroyed by construction of a building.
Another occurrence in Tishomingo County, Mississippi, was extirpated
from a site that was disturbed by construction of the Yellow Creek
Nuclear Power Plant (Shea 1992, p. 15). A third site from which the
species is considered extirpated, in Roane County, Tennessee, was
severely disturbed during highway construction (Shea 1992, p. 15). One
extant occurrence in Carroll County, Georgia, is located within a
subdivision where restrictions have been put in place to protect the
wetland habitat. Another extant occurrence in Pickens County, Georgia,
is located within a subdivision, but the wetland habitat where white
fringeless orchid occurs is located within an area protected by a
conservation easement held by the North American Land Trust. There is
one occurrence of uncertain status that is located on an as yet
undeveloped lot in a subdivision in Grundy County, Tennessee. Potential
future residential development at this site could directly impact white
fringeless orchid due to habitat conversion or ground disturbance, or
could indirectly affect the species by altering hydrology, increasing
shading, or introducing invasive, nonnative plants.
Based on our review of the best commercial and scientific data
available, development is a threat of low magnitude with potential to
affect few white fringeless orchid populations in the foreseeable
future.
Silvicultural Practices
Direct and indirect effects of silvicultural practices have
adversely affected habitat conditions and abundance of many white
fringeless orchid populations. Incompatible silviculture has taken the
form of clearcutting, both of swamps occupied by the species and of
surrounding upland forests. Shea (1992, p. 15) reported that white
fringeless orchid had been extirpated from two Alabama sites where
logging had disturbed the habitat. At one of these sites, the loss was
attributed to impacts from logging and removal of beaver dams.
While white fringeless orchid has sometimes shown short-term
increases in flower production following canopy removal, the longer-
term response typically is a decline in abundance as vegetation
succession ensues (Shea 1992, pp. 26, 96; Birchenko 2001, p. 33).
Forests have been clearcut at nine extant occurrences and two of
uncertain status in Tennessee, two extant sites and one of uncertain
status in Alabama, and one extant site in Georgia. Of these, there is
evidence for declines in white fringeless orchid abundance following
timber harvests at five extant occurrences and two of uncertain status
in Tennessee (TDEC 2014) and one extant occurrence in Alabama
(Birchenko 2001, p. 33; ANHP 2014). At some sites, the timber harvests
were too recent to know yet how white fringeless orchid will respond.
In many cases, native forests surrounding white fringeless orchid
sites have been clearcut and replaced by intensively managed pine
plantations, often consisting solely of Pinus taeda (loblolly pine),
where intensive mechanical or chemical site preparation before planting
occurs in order to reduce seedling competition with other tree species
(Clatterbuck and Ganus 1999, p. 4). Plantation forestry generally
causes reductions in streamflow as compared to native forest vegetation
(Scott 2005, p. 4204), and research from the Cumberland Plateau
comparing calcium stores in soils and trees of native hardwood forests
to mature pine on converted hardwood sites revealed calcium loss from
the system after a single pine rotation that could impede future
regrowth of the native oak-hickory forest (McGrath et al. 2004, p. 21).
The fact that plantation forests are implicated in reduced streamflow
suggests that they could reduce the hydroperiod (seasonal pattern of
the water level that results from the combination of the water budget
and the storage capacity of a wetland) in wetlands located at the heads
of streams, such as those typically occupied by white fringeless
orchids, when they are embedded in a matrix of pine plantations. While
more information on indirect effects of pine plantations on
hydroperiods of wetlands occupied by white fringeless orchid is needed,
evidence suggests that restoring native hardwood forest vegetation may
be needed to restore wetland hydrology in some sites, and that this
would be a challenging and long-term process.
[[Page 55312]]
At least four extant occurrences in Alabama, two in Georgia, and
four in Tennessee are located in wetlands that are either located in
pine plantations or bordered by them in surrounding uplands; one
Tennessee occurrence of uncertain status is similarly situated.
Fourteen percent of native forest, in seven counties of the southern
Cumberland Plateau in Tennessee that are occupied by white fringeless
orchid, was lost between 1981 and 2000. The majority (74 percent) of
this lost native forest was converted to nonnative loblolly pine
plantations, and the annual rate of conversion doubled during the last
3 years (1997-2000) (McGrath et al. 2004, p. 13). Given that there are
three extant Tennessee occurrences and two of uncertain status that are
located on private industrial forest lands, which have not yet been
converted to nonnative pine plantations, conversion of lands
surrounding additional white fringeless orchid occurrences represents a
foreseeable future threat to the species.
Based on our review of the best commercial and scientific data
available, silvicultural practices are a threat of moderate magnitude
to white fringeless orchid populations.
Invasive Plant Species
The presence of invasive, nonnative plant species, including
Microstegium vimineum (Japanese stiltgrass), Ligustrum sinense (Chinese
privet), and Perilla frutescens (beefsteak plant), has been documented
at 10 extant white fringeless orchid occurrences and one of unknown
status (U.S. Forest Service (USFS) 2008, p. 53; Richards 2013, pers.
comm.; KSNPC 2014; TDEC 2014). Chinese privet has been negatively
correlated with cover, abundance, and richness of native herbaceous
species in riparian wetlands of the Piedmont physiographic province
(Greene and Blossey 2012, p. 143). Japanese stiltgrass has been shown
to increase pH and phosphorous availability in Cumberland Plateau
forest soils (McGrath and Binkley 2009, pp. 145-153) and to increase
abundance of vesicular arbuscular mycorrhiza (VAM; mycorrhizal fungi
that grow into the roots of host plants and form specialized structures
called arbuscules and vesicles) in other sandstone-derived soils
(Kourtev et al. 2002, p. 3163) as compared to native vegetation. While
the effect of these soil alterations on white fringeless orchid has not
been investigated, the species is associated with acidic (i.e., lower
pH) soils (Zettler and Fairey 1990, p. 213) and is dependent upon a
specific mycorrhizal fungus that is not a VAM (Currah et al. 1997, p.
340). To the extent that increases in VAM might lead to decreases in
abundance of the orchid's mycorrhizal fungus, Epulorhiza inquilina,
negative effects on germination and growth would be expected for white
fringeless orchid.
In addition to threats posed by nonnative plant species, at two
extant white fringeless orchid sites, a native species, Lygodium
palmatum (American climbing fern), has demonstrated invasive
tendencies. Both sites are on public lands, and USFS attempts to
control spread of the species at one of the sites met limited success.
At the site on National Park Service lands, American climbing fern
blankets vegetation along both sides of a dirt road that is in close
proximity to a white fringeless orchid site, and the fern vines have
spread into adjacent forests, including the wetland where white
fringeless orchid occurs. Left unmanaged, encroachment of nonnative
plants and American climbing fern could reduce potential for exposure
of seeds to light before being incorporated into the soil, which
enhances germination rates (Zettler and McInnis 1994, p. 137).
Based on available data, encroachment by native and nonnative
invasive plants is a threat of moderate magnitude to white fringeless
orchid populations.
Feral Hogs
Ground disturbance by rooting of feral hogs has been observed at 13
extant white fringeless orchid occurrences, in Georgia and Tennessee,
including two of the largest known occurrences, both on protected lands
(Zettler 1994, p. 687; USFS 2008, p. 54; Richards 2013 pers. comm.;
Richards 2014, pers. comm.; Tackett 2015, pers. comm.). These
disturbances have affected specific microsites where white fringeless
orchid had previously been observed growing, as well as surrounding
wetland habitat. Disturbance by feral hogs has been shown to affect
plant communities by causing decreases in plant cover, diversity, and
regeneration; effects to fungi from feral hogs are also known to occur
(Barrios-Garcia and Ballari 2012, p. 2295), suggesting potential for
adverse effects to white fringeless orchid via disruption of the
symbiotic interactions with mycorrhizal fungi that enhance seed
germination and promote seedling development and establishment (Zettler
and McInnis 1992, pp. 157-160; Rasmussen and Whigham 1993, p. 1374).
Based on our review of the best commercial and scientific data
available, feral hogs are a threat of moderate magnitude to white
fringeless orchid populations.
Excessive Shading
Despite the fact that white fringeless orchid habitat has been
described as shaded (Luer 1975, p. 186; Zettler and Fairey 1990, p.
212; Shea 1992, p. 19), excessive shading due to vegetation succession
has been recognized as a factor associated with population declines
(Shea 1992, pp. 26, 55, 61, 69; Richards 2013, pers. comm.; Schotz
2015, p. 4), and succession of woody vegetation has been named as the
primary factor in the decline of Tennessee populations (TDEC 2012, p.
3). One Tennessee occurrence was extirpated due to woody vegetation
succession in a right-of-way that occurred following removal of a
powerline (TDEC 2014). Available data indicate that this threat has
been noted at 19 extant occurrences and 5 of uncertain status across
the species' geographic range (Richards 2013, pers. comm.; Sullivan
2014, pers. comm.; KSNPC 2014; TDEC 2014; Schotz 2015, pp. 10-35). The
threat of shading has been most often noted in instances where woody
succession followed logging in or adjacent to sites occupied by white
fringeless orchid. As noted above, white fringeless orchid occurrences
often exhibit short-term increases in flower production following
canopy removal, but the longer-term response typically is a decline in
abundance as woody vegetation succession ensues (Shea 1992, pp. 26, 96;
Birchenko 2001, p. 33; TDEC 2012, pp. 2-3). It has been suggested that
fire could play a role in regulating woody vegetation growth in uplands
surrounding white fringeless orchid habitats, allowing greater light
penetration into swamps where the species grows (Schotz 2015, p. 4).
Based on our review of the best commercial and scientific data
available, excessive shading is a threat of moderate magnitude to white
fringeless orchid populations.
Altered Hydrology
Several factors have been identified as causes for altered
hydrology in white fringeless orchid habitat, including pond
construction (TDEC 2008, p. 4), ditching (Sullivan 2014, pers. comm.),
development, logging (Shea 1992, p. 26; Taylor 2014, pers. comm.), and
woody vegetation succession following logging (Hoy 2012, p. 13). In
Tennessee, three white fringeless orchid sites have been destroyed by
pond construction, one as recently as 2006 (TDEC 2008, p. 4). One site
in Cobb County, Georgia, was destroyed by pond construction
[[Page 55313]]
(Richards 2014, pers. comm.). In Winston County, Alabama, hydrology was
altered by the removal of beaver dams to facilitate a logging
operation, causing the extirpation of a white fringeless orchid
occurrence (Shea 1992, p. 25).
Altered hydrology has been noted as a threat at five extant
occurrences and four of unknown status (Taylor 2014, pers. comm.;
Sullivan 2014, pers. comm.; GDNR 2014; KSNPC 2014; TDEC 2014).
Conversion of surrounding uplands to a pine plantation was noted as the
cause for hydrologic alteration at one extant site in Georgia (GDNR
2014), and as noted above, is a condition that is present at nine other
extant occurrences and one of unknown status. Logging in surrounding
uplands is suspected of contributing to altered hydrology at two
Kentucky occurrences, one extant and one of uncertain status (Taylor
2014, pers. comm.; KSNPC 2014), by causing increased surface runoff
during heavy precipitation events and accelerating channel development
in wetlands at stream heads. In addition to loss of white fringeless
orchid habitat and occurrences due to pond construction at the three
Tennessee sites discussed above, hydrology has been altered in wetland
habitats down slope of ponds at two other Tennessee sites, where white
fringeless orchid's status is now uncertain (TDEC 2014). In
Mississippi, ditching has altered hydrology at a site where white
fringeless orchid was discovered in 2011, leaving the species' status
uncertain at this location (Sullivan 2014, pers. comm.). Ditching has
also altered hydrology at an extant occurrence located adjacent to a
State highway in Tennessee. Disturbance by heavy equipment in an
adjacent powerline right-of-way is thought to have altered hydrology at
an extant site in Kentucky, by causing rutting of soils and hastening
channel development at the stream head (Taylor 2014, pers. comm.).
While most observations of threats related to logging activity have
concerned habitat disturbance or increased shading caused by woody
vegetation regrowth, Hoy (2012, p. 26) suggests that high stem
densities that occur during succession following canopy removal shorten
the hydroperiod of wetlands at an extant white fringeless orchid site
in Kentucky. This results from increased evapotranspiration, due to
greater leaf surface area, causing faster rates of water loss. While
only empirically documented in wetlands where a single white fringeless
orchid occurrence is located, this process likely has affected numerous
other sites where canopy removal has occurred due to logging.
Based on our review of the best commercial and scientific data
available, altered hydrology is a threat of moderate magnitude to white
fringeless orchid populations.
Right-of-Way Maintenance
Eleven extant white fringeless orchid occurrences and one of
uncertain status are located in transportation or utility rights-of-way
(Richards 2013, pers. comm.; KSNPC 2014; TDEC 2014). Vegetation
management practices in such habitats prevent advanced succession of
woody vegetation, which can benefit white fringeless orchid by
periodically reducing shading. On the other hand, mechanical clearing
in these habitats can alter hydrology by causing rutting of soils and
hastening channel development, as discussed in the preceding section
(Taylor 2014, pers. comm.). Mowing during the flowering period for
white fringeless orchid is detrimental, given the low flowering rates
that have been observed in this species and the fact that individual
plants will not regenerate flowers during a growing season once they
are lost to herbivory or other causes (Sheviak 1990, p. 195). Also, it
is likely that indiscriminate herbicide application would cause
mortality of white fringeless orchid plants. However, we have knowledge
of one event in which the species responded favorably following
selective herbicide application to control woody plant succession in a
Tennessee Valley Authority transmission line right-of-way, reaching
record numbers of flowering plants documented at the site within 2
years following the herbicide treatment. The lack of adverse effect to
white fringeless orchid in this instance is likely attributable to the
targeted application of herbicides to woody plants only.
Based on our review of the best commercial and scientific data
available, right-of-way maintenance is a threat of moderate magnitude
to white fringeless orchid populations.
Conservation Efforts To Reduce Habitat Destruction, Modification, or
Curtailments of Its Range
The USFS has undertaken efforts to restore or protect habitat at a
number of white fringeless orchid sites located on National Forest (NF)
lands. At the Cherokee NF, the USFS constructed fences to exclude feral
hogs at two sites, one of which is the largest known occurrence of the
species. These fences are effective when maintained; however, only the
main concentration of plants is protected at the site where the largest
occurrence is present. At the Daniel Boone NF, the installation of
check dams (small, often temporary, dam constructed across a swale,
drainage ditch, or waterway to counteract erosion by reducing water
flow velocity) in 2005 has been somewhat effective in restoring
suitable conditions for white fringeless orchid at a site where wetland
hydrology had been altered. Efforts to control invasion by Japanese
stiltgrass by repeatedly weeding at one site on Daniel Boone NF have
been hampered by a seed source that exists on private lands upslope of
the site (Taylor 2014, pers. comm.).
Efforts have been made to restore suitable habitat conditions at
one site on KSNPC lands, by reducing woody stem encroachment in 2012,
following a timber harvest, and by placing log dams to slow surface
runoff and minimize channel development. To date, white fringeless
orchid has not shown a measureable response to this management effort;
despite large numbers of vegetative Platanthera spp. leaves being
present, fewer than 30 flowering plants per year have been observed in
recent years at this site, where 530 plants were observed flowering in
1998 (KSNPC 2014).
Summary of Factor A
The threats to white fringeless orchid from habitat destruction and
modification are occurring throughout much of the species' range. These
threats include development, silvicultural practices, invasive plant
species, disturbance by feral hogs, shading due to understory and
canopy closure, altered hydrology, and right-of-way maintenance. While
the species is present in a number of sites on conservation lands, few
conservation actions have been undertaken to address these threats to
the species' habitat, and those that are described above have met with
limited success. The population-level impacts of habitat destruction
and modification are expected to continue. Threats related to
silvicultural practices could increase in the future, given that some
occurrences are located on private industrial forest lands, where
logging and future conversion of native hardwood forests to pine
plantation are likely to occur. In addition to physical disturbances
that alter hydrology, predicted changes in precipitation and drought
frequency and severity (see Factor E, below) may contribute to
increased loss of suitable habitat in the future.
Based on our review of the best commercial and scientific data
available, we conclude that the present
[[Page 55314]]
or threatened destruction, modification, and curtailment of its habitat
or range is currently a threat to white fringeless orchid and is
expected to continue and possibly increase in the future.
Factor B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
White fringeless orchid was first collected from a site in McCreary
County, Kentucky, but had disappeared from the site by the 1940s,
apparently due to the collection of hundreds of specimens to be
deposited in herbaria (Ettman and McAdoo 1979 cited in Zettler and
Fairey 1990, p. 212). Shea (1992, p. 27) cites personal communications
from R. Smartt and P. Somers, the latter of whom was a botanist with
Tennessee's Natural Heritage Program, reporting that two nurseries in
Tennessee had collected white fringeless orchid plants for resale.
While we are not able to independently verify these historical reports,
they suggest that collecting for various purposes has long been a
threat to white fringeless orchid. Evidence of recent plant collecting
(for unknown purposes), at two separate locations, is presented below.
The first of these occurred in 2004, alongside a State highway in
Chattooga County, Georgia. Botanists discovered many flowering plants
at the site, but when they later returned to the site they found that
most of the plants had been dug out and removed. During 2014, only a
single non-flowering white fringeless orchid was seen at this site
(Richards 2014, pers. comm.). The second incident took place during
2014, alongside a State highway in Sequatchie County, Tennessee. A
Service biologist observed 83 flowering white fringeless orchids at
this site on August 13, 2014, but 2 weeks later only 31 plants bearing
flowers or fruiting capsules were found during a survey with TDEC
botanists. In the location where the greatest concentration of
flowering plants had been observed on August 13, there were areas where
mats of sphagnum moss and roots of woody plants had been scraped away
from the surface and shallow depressions were present in the mineral
soil beneath. Because no wildlife tracks were present in the area where
the surface disturbance had occurred and no partial stems were present
to indicate that the loss resulted from herbivory, the Service and TDEC
botanists concluded that the plants had been collected.
While the fate of plants that have been collected is not known, we
received information about white fringeless orchids having been
purchased via an online vendor in 2004 (Richards 2014, pers. comm.).
The plants were sold as nursery grown Platanthera blephariglottis
(white fringed orchid), a taxon of which white fringeless orchid was
once treated as a variety (Correll 1941, pp. 153-157); however, when
the plants later flowered in a greenhouse, it was apparent they were
white fringeless orchids. When the seller was questioned about the
origin of the plants, she initially insisted they had come from a
friend's private lands. The seller later refused to respond to
additional inquiries from the buyer. A recent online search for
commercially available, native Platanthera orchids revealed that three
species, which often co-occur with white fringeless orchid, were being
offered for sale on the online auction and shopping Web site eBay
(www.ebay.com, accessed on September 17, 2014). The unintended purchase
of white fringeless orchid from an online vendor, combined with the
offering of three other Platanthera orchids for sale via eBay, provides
additional evidence that demand exists for native orchids of this
genus.
Due to the species' rarity, the small sizes of most known
populations, and the fact that most of the populations are located in
remote sites that are infrequently monitored by conservation
organizations or law enforcement, collection is a threat to P.
integrilabia. In small populations, the collection of even a few
individuals would diminish reproductive output and likely reduce
genetic diversity.
Based on our review of the best commercial and scientific data
available, overutilization for commercial, scientific, or recreational
purposes is currently a threat of low magnitude to white fringeless
orchid and is expected to continue in the future. If the Service were
to publish a proposal to designate critical habitat for this species,
which would include detailed maps and descriptions of locations where
the species is present, the magnitude and severity of this activity
would increase, and it would become a threat of moderate to high
magnitude.
Factor C. Disease or Predation
Zettler and Fairey (1990, p. 214) reported that both herbivory and
disease affected two white fringeless orchid populations they studied
in Georgia and South Carolina. At the Georgia site, 16.5 percent of the
white fringeless orchids suffered from herbivory and 11.5 percent from
disease; at the South Carolina site, herbivory and disease were evident
on 22.5 and 23.9 percent of the plants, respectively. The specific
herbivores were not discussed, but disease was attributed to pathogenic
fungi that were isolated from necrotic tissue, including species of
Alternaria, Pestalotia, Nigrospora, and Cercospora (Zettler and Fairey
1990, p. 214).
Zettler (1994, p. 687) also reported observations of tuber
herbivory by feral hogs at the largest white fringeless orchid
occurrence in McMinn County, Tennessee. The USFS constructed fences to
exclude hogs from the greatest concentration of plants at this site and
at a smaller occurrence in Polk County, but found the fence at the
McMinn County site in need of repair in 2002, when they discovered that
approximately half of the flowering white fringeless orchids and many
vegetative orchids had been uprooted (USFS 2008, p. 54). As noted
above, evidence of feral hog disturbance has been observed at 10 extant
white fringeless orchid sites.
Numerous observers have reported herbivory by deer as a threat to
white fringeless orchids, specifically removal of inflorescences from
white fringeless orchid plants (Zettler and Fairey 1990, p. 212; Shea
1992, pp. 27, 61, 71-77, 95-97; TDEC 2012, p. 3; KSNPC 2014; TDEC
2014). From these sources, we found observations of inflorescence
herbivory at 21 extant occurrences and 5 where the status is now
uncertain. It is likely that this threat affects most white fringeless
orchid occurrences (TDEC 2012, p. 3), despite not having been
specifically documented in every instance.
Using material supplied by the Service, TDEC biologists installed
plastic deer control fencing around two areas with concentrations of
white fringeless orchids at a site on Tennessee State Park lands in
2013. During 2014, there were 105 flowering plants at the site, plus 31
plants with browsed inflorescences found outside of the fenced
enclosures and one browsed plant inside one of the enclosures where the
fence had partially collapsed. Inside of the enclosures were 45
flowering plants that were unharmed. Approximately one-third of the
flowering plants outside of the fenced areas suffered inflorescence
herbivory.
The high frequency at which inflorescence herbivory has been
observed at white fringeless orchid occurrences likely contributes to
population declines in this species. Orchid growth is initiated each
spring from overwintered buds, similar to most perennial plants;
however, orchids differ from most other plants by lacking the capacity
to replace tissues lost to herbivory or other causes until the
following year. In addition, in several
[[Page 55315]]
species of Platanthera, the usual response to loss of the shoot is
death of the plant (Sheviak 1990, p. 195).
Based on our review of the best commercial and scientific data
available, predation is a threat of moderate to high magnitude to white
fringeless orchid and is expected to continue in the future. Pathogenic
fungi have been documented in only two populations, though their
presence has likely been overlooked by most observers, and therefore
they are a low magnitude threat.
Factor D. The Inadequacy of Existing Regulatory Mechanisms
Section 4(b)(1)(A) of the Act requires the Service to take into
account ``those efforts, if any, being made by any State or foreign
nation, or any political subdivision of a State or foreign nation, to
protect such species. . . .'' In relation to Factor D under the Act, we
interpret this language to require the Service to consider relevant
Federal, State, and tribal laws, plans, regulations, and other such
mechanisms that may minimize any of the threats we describe in threat
analyses under the other four factors, or otherwise enhance
conservation of the species. We give strongest weight to statutes and
their implementing regulations and to management direction that stems
from those laws and regulations. An example would be State governmental
actions enforced under a State statute or constitution, or Federal
action under statute.
Having evaluated the significance of the threat as mitigated by any
such conservation efforts, we analyze under Factor D the extent to
which existing regulatory mechanisms are inadequate to address the
specific threats to the species. Regulatory mechanisms, if they exist,
may reduce or eliminate the impacts from one or more identified
threats. In this section, we review existing State and Federal
regulatory mechanisms to determine whether they effectively reduce or
remove threats to the white fringeless orchid.
The white fringeless orchid is listed as special concern, with
historical status, by the State of North Carolina, as threatened by the
State of Georgia, and as endangered by the Commonwealth of Kentucky and
State of Tennessee.
The North Carolina Plant Protection and Conservation Act (NCPPCA;
North Carolina General Statutes 106-202) authorizes the North Carolina
Plant Conservation Board, within the Department of Agriculture and
Consumer Services, to among other things: Maintain a list of protected
plant species; adopt regulations to protect, conserve, or enhance
protected plant species; and regulate the sale or distribution of
protected plant species. The NCPPCA forbids any person from uprooting,
digging, taking or otherwise disturbing or removing protected plant
species from the lands of another without a written permit and
prescribes penalties for violations.
The law that provides official protection to designated species of
plants in Georgia is known as the Wildflower Preservation Act of 1973.
Under this State law, no protected plant may be collected without
written landowner permission. No protected plant may be transported
within Georgia without a transport tag with a permit number affixed.
Permits are also used to regulate a wide array of conservation
activities, including plant rescues, sale of protected species, and
propagation efforts for augmenting natural populations and establishing
new ones. No protected plants may be collected from State-owned lands
without the express permission of the GDNR. The Georgia Environmental
Policy Act (GEPA), enacted in 1991, requires that impacts to protected
species be addressed for all projects on State-owned lands, and for all
projects undertaken by a municipality or county if funded half or more
by State funds, or by a State grant of more than $250,000. The
provisions of GEPA do not apply to actions of non-governmental
entities. On private lands, the landowner has ultimate authority on
what protection efforts, if any, occur with regard to protected plants
(Patrick et al. 1995, p. 1 of section titled ``Legal Overview'').
The Kentucky Rare Plants Recognition Act, Kentucky Revised Statutes
(KRS), chapter 146, sections 600-619, directs the KSNPC to identify
plants native to Kentucky that are in danger of extirpation within
Kentucky and report every 4 years to the Governor and General Assembly
on the conditions and needs of these endangered or threatened plants.
This list of endangered or threatened plants in Kentucky is found in
Kentucky Administrative Regulations, title 400, chapter 3:040. The
statute (KRS 146:600-619) recognizes the need to develop and maintain
information regarding distribution, population, habitat needs, limiting
factors, other biological data, and requirements for the survival of
plants native to Kentucky. This statute does not include any regulatory
prohibitions of activities or direct protections for any species
included in the list. It is expressly stated in KRS 146.615 that this
list of endangered or threatened plants shall not obstruct or hinder
any development or use of public or private land. Furthermore, the
intent of this statute is not to ameliorate the threats identified for
the species, but it does provide information on the species.
The Tennessee Rare Plant Protection and Conservation Act of 1985
(TRPPCA; Tennessee Code Annotated 11-26-201) authorizes the Tennessee
Department of Environment and Conservation (TDEC) to, among other
things: Conduct investigations on species of rare plants throughout the
State of Tennessee; maintain a listing of species of plants determined
to be endangered, threatened, or of special concern within the State;
and regulate the sale or export of endangered species via a licensing
system. The TRPPCA forbids persons from knowingly uprooting, digging,
taking, removing, damaging, destroying, possessing, or otherwise
disturbing for any purpose, any endangered species from private or
public lands without the written permission of the landowner, lessee,
or other person entitled to possession and prescribes penalties for
violations. The TDEC may use the list of threatened and special concern
species when commenting on proposed public works projects in Tennessee,
and the department encourages voluntary efforts to prevent the plants
on this list from becoming endangered species. This authority is not,
however, to be used to interfere with, delay, or impede any public
works project.
Thus, despite the fact that the white fringeless orchid is listed
as special concern, threatened, or endangered by the States of Georgia,
North Carolina, and Tennessee and the Commonwealth of Kentucky, these
designations confer no guarantee of protection to the species' habitat,
whether on privately owned or State-owned lands, unless such
protections are voluntarily extended to the species, and only prohibit
unauthorized collection in Georgia, North Carolina, and Tennessee.
Section 404 of the Clean Water Act (CWA; 33 U.S.C. 1251 et seq.)
establishes a Federal program for regulating the discharge of dredged
or fill material into waters of the United States, including wetlands.
Additionally, section 401 of the CWA forbids Federal agencies from
issuing a permit or license for activities that may result in a
discharge to waters of the United States until the State or Tribe where
the discharge would originate has granted or waived certification. All
of the States where white fringeless orchid occurs maintain regulatory
programs providing a framework for issuance of section 401
certifications related to applications for section 404 permits.
[[Page 55316]]
This legislation does not prohibit the discharge of these materials
into wetlands; rather, it provides a regulatory framework that requires
permits prior to such action being taken. The U.S. Army Corps of
Engineers (Corps) reviews individual permits for potentially
significant impacts; however, most discharges are considered to have
minimal impacts and may be covered by a general permit that does not
require individual review.
Due to their typical position in non-navigable heads of streams
located remotely from traditional navigable waters, where flow is
ephemeral or intermittent and channels are poorly defined, if present
at all, wetlands where white fringeless orchid occurs have been
considered to not exhibit a significant nexus with traditional
navigable waters. Therefore, these types of wetlands typically do not
meet the definition of waters of the United States given in the
Environmental Protection Agency (EPA) and Corps joint memorandum Clean
Water Act Jurisdiction Following the U.S. Supreme Court's Decision in
Rapanos v. United States & Carabell v. United States (December 2,
2008). However, on June 29, 2015, the EPA and Corps published a final
rule (80 FR 37054) that revises the definition of ``Waters of the
United States.'' Specific guidance on implementation of this revised
definition is currently lacking, but it appears that the revised
definition now includes the habitats where white fringeless orchid
occurs among waters of the United States.
While the wetland habitats occupied by white fringeless orchid are
now likely to be included within the definition of waters of the United
States, as noted above, section 404 of the CWA does not necessarily
prevent degradation to such habitats from the discharge of dredge or
fill material. It simply provides a regulatory program for permitting
activities that would result in such a discharge. Further, discharges
associated with normal farming, ranching, and forestry activities, such
as plowing, cultivating, minor drainage, and harvesting for the
production of food, fiber, and forest products are exempt from the
requirement to obtain a permit. Thus, potential impacts to wetland
habitats from silvicultural activities such as those described above in
the Factor A discussion are not regulated under section 404 of the CWA.
Factor E. Other Natural or Manmade Factors Affecting Its Continued
Existence
Small Population Size
The low number of individuals that have been seen at most white
fringeless orchid occurrences (Figure 1, above) increases the species'
vulnerability to threats, discussed under Factors A through D, above,
by diminishing its resilience to recover from demographic reductions
caused by habitat disturbance or modification, collecting, or
herbivory. Despite the fact that white fringeless orchid has been shown
to be self-compatible, higher rates of fruit set have been observed in
larger populations, presumably due to higher rates of cross-pollination
(Zettler and Fairey 1990, p. 214; Zettler et al. 1996, p. 20). Zettler
et al. (1996, p. 22) attributed the lower fruiting rates in the smaller
populations to inbreeding depression, noting that in a separate study
both germination rates and propagation success were greater in white
fringeless orchid seeds collected from the largest of the three
populations they studied (Zettler and McInnis 1992, p. 160). Johnson et
al. (2009, p. 3) found that higher proportions of self-pollination
occurred in smaller populations of a moth-pollinated orchid, Satyrium
longicauda (no common name), presumably due to pollinators visiting
more flowers per plant in smaller populations and more frequently
transferring pollen among flowers within a single inflorescence, rather
than frequently moving among separate inflorescences on different
individuals. To the extent that rates of cross-pollination, fruit set,
germination, and propagation success are lower for white fringeless
orchid populations of small size, demographic reductions resulting from
other threats place the species at greater risk of localized
extinctions.
While the results of genetic analyses did not demonstrate that
genetic variability in populations of white fringeless orchid has been
eroded by restricted gene flow, Birchenko (2001, pp. 34-40) cautioned
that interactions between demographic and ecological factors could be a
cause for some of the declines in white fringeless orchid population
sizes and could ultimately cause declines in the species' genetic
variation and increase differentiation among its populations. The
ability of populations to adapt to environmental change is dependent
upon genetic variation, a property of populations that derives from its
members possessing different forms (i.e., alleles) of the same gene
(Primack 1998, p. 283). Small populations occurring in isolation on the
landscape can lose genetic variation due to the potentially strong
influence of genetic drift, i.e., the random change in allele frequency
from generation to generation (Barrett and Kohn 1991, p. 8). Smaller
populations experience greater changes in allele frequency due to drift
than do larger populations (Allendorf and Luikart 2007, pp. 121-122).
Loss of genetic variation due to genetic drift heightens susceptibility
of small populations to adverse genetic effects, including inbreeding
depression and loss of evolutionary flexibility (Primack 1998, p. 283).
Deleterious effects of loss of genetic variation through drift have
been termed drift load, which is expressed as a decline in mean
population performance of offspring in small populations (Willi et al.
2005, p. 2260).
Climate Change
Our analyses under the Act include consideration of ongoing and
projected changes in climate. The terms ``climate'' and ``climate
change'' are defined by the Intergovernmental Panel on Climate Change
(IPCC). ``Climate'' refers to the mean and variability of different
types of weather conditions over time, with 30 years being a typical
period for such measurements, although shorter or longer periods also
may be used (IPCC 2014, pp. 119-120). 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 2014, pp. 119-
120). A recent compilation of climate change and its effects is
available from reports of the IPCC (IPCC 2014, entire).
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). Projected changes in climate and related impacts can vary
substantially across and within different regions of the world (e.g.,
IPCC 2014, pp. 11-13). Therefore, we use ``downscaled'' projections
when they are available and have been developed through appropriate
scientific procedures (see Glick et al. 2011, pp. 58-61, for a
discussion of downscaling). In our analyses, we use our expert judgment
to weigh relevant information, including uncertainty, in our
[[Page 55317]]
consideration of various aspects of climate change.
The IPCC concluded that evidence of warming of the climate system
is unequivocal (IPCC 2014, pp. 2, 40). Numerous long-term climate
changes have been observed including changes in arctic temperatures and
ice, widespread changes in precipitation amounts, ocean salinity, and
aspects of extreme weather including heavy precipitation and heat waves
(IPCC 2014, pp. 40-44). While continued change is certain, the
magnitude and rate of change is unknown in many cases. Species that are
dependent on specialized habitat types, are limited in distribution, or
have become restricted to the extreme periphery of their range will be
most susceptible to the impacts of climate change.
Estimates of the effects of climate change using available climate
models lack the geographic precision needed to predict the magnitude of
effects at a scale small enough to discretely apply to the range of
white fringeless orchid (i.e., there are no ``downscaled'' projections
available). However, data on recent trends and predicted changes for
the Southeast United States (Karl et al. 2009, pp. 111-122) provide
some insight for evaluating the potential threat of climate change to
the species. White fringeless orchid's geographic range lies within the
geographic area included by Karl et al. (2009, pp. 111-116) in their
summary of regional climate impacts affecting the Southeast region.
Since 1970, the average annual temperature across the Southeast has
increased by about 2 degrees Fahrenheit ([deg]F), with the greatest
increases occurring during winter months. The geographic extent of
areas in the Southeast region affected by moderate to severe spring and
summer drought has increased over the past three decades by 12 and 14
percent, respectively (Karl et al. 2009, p. 111). These trends are
expected to increase. Rates of warming are predicted to more than
double in comparison to what the Southeast has experienced since 1975,
with the greatest increases projected for summer months. Depending on
the emissions scenario used for modeling change, average temperatures
are expected to increase by 4.5 [deg]F to 9 [deg]F by the 2080s (Karl
et al. 2009, p. 111). While there is considerable variability in
rainfall predictions throughout the region, 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,
intensity, and duration of drought events (Karl et al. 2009, p. 112).
Depending on timing and intensity of drought events, white
fringeless orchid occurrences could be adversely affected by increased
mortality rates, reduced reproductive output due to loss or reduced
vigor of mature plants, and reduced rates of seed germination and
seedling recruitment. Further, white fringeless orchid's dependence
upon a limited number of large Lepidoptera for pollination (Zettler et
al. 1996, pp.16-22) and, potentially, on a single species of
mycorrhizal fungi to complete its life cycle (Currah et al. 1997, p.
340) place the species at higher risk of extinction due to
environmental changes that could diminish habitat suitability for it or
the other species upon which it depends (Swarts and Dixon 2009, p.
546).
While climate has changed in recent decades in the southeastern
United States and the rate of change likely will continue to increase
into the future, we do not have data to determine specifically how the
habitats where white fringeless orchid occurs will be affected by, or
how the species will respond to, these changes. However, the potential
for adverse effects to white fringeless orchid, either through changes
in habitat suitability or by affecting populations of pollinators or
mycorrhizal fungi, is likely to increase as climate continues to change
at an accelerating rate.
Based on our review of the best commercial and scientific data
available, diminished resilience of many occurrences due to small
population sizes and the species' dependence on a limited number of
Lepidoptera and a single species of fungi to complete its life cycle
are currently threats of moderate magnitude to white fringeless orchid.
These threats are expected to continue and, in light of climate change
projections, possibly increase in the future.
Proposed Determination
We have carefully assessed the best scientific and commercial
information available regarding the past, present, and future threats
to the white fringeless orchid. Habitat destruction and modification
(Factor A) from development, silvicultural practices, excessive
shading, and altered hydrology (i.e., pond construction, beaver dam
removal) have resulted in extirpation of the species from 10 sites.
These threats, in addition to invasive plant species, feral hogs, and
right-of-way maintenance, are associated with habitat modifications
affecting dozens of other occurrences that are extant or of uncertain
status. Collecting for scientific, recreational, or commercial purposes
(Factor B) has been attributed as the cause for extirpation of white
fringeless orchid at its type locality, and recent evidence
demonstrates that this activity remains a threat to this species.
Fungal pathogens have been identified as a threat to white fringeless
orchid, but a threat with potentially greater impact associated with
Factor C is inflorescence herbivory, presumably by deer, which has been
reported at over one-third of extant occurrences and likely is a factor
threatening most white fringeless orchid occurrences, especially where
low numbers of plants are present. Tuber herbivory by feral hogs has
been reported at the largest known white fringeless orchid occurrence.
The effects of these threats are intensified by the small population
sizes that characterize a majority of occurrences throughout the
species' geographic range (Factor E), due to their diminished
resilience to recover from demographic reductions caused by loss of
individuals or low reproductive output from other threats. Further, the
species' dependence on a limited number of Lepidoptera and a single
species of fungi to complete its life cycle, make it vulnerable to
disturbances that diminish habitat suitability for these taxa as well
(Factor E). Existing regulatory mechanisms have not led to a reduction
or removal of threats posed to the species from these factors (see
Factor D discussion).
The Act defines an endangered species as any species that is ``in
danger of extinction throughout all or a significant portion of its
range'' and a threatened species as any species ``that is likely to
become endangered throughout all or a significant portion of its range
within the foreseeable future.'' We find that white fringeless orchid
is likely to become endangered throughout all or a significant portion
of its range within the foreseeable future based on the low to moderate
threats currently impacting the species. The species is known to be
extant at 58 locations, but low numbers of individuals have been
observed at more than half of these (see Figure 1, above), distributed
across the species' range, and their persistence into the future is
uncertain. Furthermore, the threats of habitat destruction or
modification and herbivory are present throughout the species'
geographic range. Left unmanaged, these threats will likely lead to
further reductions in the species' geographic range and abundance at
individual sites, increasing the risk of extinction to the point of
endangerment. Therefore, on the basis of the best available scientific
and commercial information, we
[[Page 55318]]
propose listing the white fringeless orchid as threatened in accordance
with sections 3(20) and 4(a)(1) of the Act. The species does not
currently meet the definition of endangered, because a sufficient
number of robust populations are present on publicly owned or managed
lands. Conservation efforts have been initiated that could be effective
in reducing threats by increasing population sizes and improving
habitat conditions across much of the species' geographic range.
Under the Act and our implementing regulations, a species may
warrant listing if it is endangered or threatened throughout all or a
significant portion of its range. The threats to the survival of white
fringeless orchid occur throughout the species' range and are not
restricted to any particular significant portion of that range.
Accordingly, our assessment and proposed determination applies to the
species throughout its entire range. Therefore, because we have
determined that white fringeless orchid is threatened throughout all of
its range, no portion of its range can be ``significant'' for purposes
of the definitions of ``endangered species'' and ``threatened
species.'' See the Final Policy on Interpretation of the Phrase
``Significant Portion of Its Range'' in the Endangered Species Act's
Definitions of ``Endangered Species'' and ``Threatened Species'' (79 FR
37578; July 1, 2014).
Critical Habitat and Prudency Determination
Critical habitat is defined in section 3 of the Act as:
(1) The specific areas within the geographic area occupied by the
species, at the time it is listed in accordance with the Act, on which
are found those physical or biological features:
(a) Essential to the conservation of the species, and
(b) Which may require special management considerations or
protection; and
(2) Specific areas outside the geographical area occupied by the
species at the time it is listed, upon a determination that such areas
are essential for the conservation of the species.
Conservation, as defined under section 3 of the Act, means to use
and the use of all methods and procedures that are necessary to bring
an endangered or threatened species to the point at which the measures
provided pursuant to the Act are no longer necessary.
Section 4(a)(3) of the Act, as amended, and implementing
regulations (50 CFR 424.12), require that, to the maximum extent
prudent and determinable, the Secretary shall designate critical
habitat at the time the species is determined to be an endangered or
threatened species. Our regulations (50 CFR 424.12(a)(1)) state that
the designation of critical habitat is not prudent when one or both of
the following situations exist:
(1) The species is threatened by taking, collection, or other human
activity, and identification of critical habitat can be expected to
increase the degree of threat to the species, or
(2) Such designation of critical habitat would not be beneficial to
the species.
We have determined that white fringeless orchid is threatened by
taking, collection, or other human activity and that identification of
critical habitat would be expected to increase this threat. We also
have determined that little measurable benefit to the species would
result from designation of critical habitat. This determination
involves weighing the expected increase in threats associated with a
critical habitat designation against the benefits gained by a critical
habitat designation. An explanation of this ``balancing'' evaluation
follows.
Increased Threat to the Species by Designating Critical Habitat
Designation of critical habitat requires publication of maps and a
narrative description of specific critical habitat areas in the Federal
Register. The degree of detail in those maps and boundary descriptions
is far greater than the general location descriptions provided in this
listing proposal. Also, while general location data (e.g., names of
administrative units of the National Park Service (NPS), USFS, or State
conservation agencies where the species occurs) concerning white
fringeless orchid are available, maps or detailed descriptions are not
found in scientific or popular literature, current agency management
plans, or other readily available sources. One exception is the
availability online of a now expired management plan for a site in
Alabama with maps depicting two locations of the species. Location
information can also be found in a journal article for a site in North
Carolina, where the species is no longer extant. Designation of
critical habitat would more widely announce the exact location of the
white fringeless orchid to poachers, collectors, and vandals and
further facilitate unauthorized collection. Due to its rarity (low
numbers of individuals in most populations), this orchid is highly
vulnerable to collection. Removal of individuals from extant
populations would have devastating consequences in terms of reducing
their viability, if not causing outright extirpation. These threats
would be exacerbated by the publication of maps and descriptions
outlining the specific locations of this imperiled orchid in the
Federal Register and local newspapers. Maps and descriptions of
critical habitat, such as those that would appear in the Federal
Register if critical habitat were designated, are not now available to
the general public.
We have discussed evidence related to poaching and commercial sale
of white fringeless orchid and other congeners above (see Factor B,
above). Due to the species' rarity, the small sizes of most known
populations, and the fact that most of the populations are located in
remote sites that are infrequently monitored by conservation
organizations or law enforcement, collection is a threat to white
fringeless orchid. In small populations, the collection of even a few
individuals would diminish reproductive output and likely reduce
genetic diversity. Identification of critical habitat would increase
the magnitude and severity of this threat by spatially depicting
exactly where the species may be found and widely publicizing this
information, exposing these fragile populations and their habitat to
greater risks. We have reviewed management plans and other documents
produced by Federal and State conservation agencies and scientific
literature, and detailed information on the specific locations of white
fringeless orchid sites is not currently available.
Benefits to the Species From Critical Habitat Designation
It is true that designation of critical habitat for endangered or
threatened species could have some beneficial effects. Section 7(a)(2)
of the Act requires Federal agencies, including the Service, to ensure
that actions they fund, authorize, or carry out are not likely to
jeopardize the continued existence of any endangered or threatened
species or result in the destruction or adverse modification of that
species' critical habitat. Critical habitat only provides protections
where there is a Federal nexus, that is, those actions that come under
the purview of section 7 of the Act. Critical habitat designation has
no application to actions that do not have a Federal nexus. Section
7(a)(2) of the Act mandates that Federal agencies, in consultation with
the Service, evaluate the effects of its proposed action on any
designated critical habitat. Similar to the Act's requirement that a
Federal agency action not jeopardize the
[[Page 55319]]
continued existence of listed species, Federal agencies have the
responsibility not to implement actions that would destroy or adversely
modify designated critical habitat. Critical habitat designation alone,
however, does not require that a Federal action agency implement
specific steps toward species recovery.
Available data indicate that white fringeless orchid is known from
58 extant occurrences and from 22 others whose current status is
uncertain. Of these 80 occurrences, 17 are located on Federal lands
managed by the USFS (12), NPS (3), and the Service (2), where they
currently receive protection from adverse effects of management actions
and, in some cases, receive management specifically to benefit the
species and its habitat. Management efforts have taken place to control
feral hogs and invasive plants, increase light availability by reducing
woody vegetation cover, and restore hydrology. In addition, the USFS
recently entered a Master Stewardship Agreement with the Atlanta
Botanical Garden to provide for habitat management, captive
propagation, and reintroduction or augmentation of populations on USFS
lands, where appropriate. Some of the populations on Federal lands are
the largest known, and any future activity involving a Federal action
that would destroy or adversely modify critical habitat at these sites
would also likely jeopardize the species' continued existence.
Consultation with respect to critical habitat would provide additional
protection to a species only if the agency action would result in the
destruction or adverse modification of the critical habitat but would
not jeopardize the continued existence of the species. In the absence
of a critical habitat designation, areas that support white fringeless
orchid will continue to be subject to conservation actions implemented
under section 7(a)(1) of the Act and to the regulatory protections
afforded by the section 7(a)(2) jeopardy standard, as appropriate.
Another possible benefit to white fringeless orchid from
designating critical habitat would be that it could serve to educate
landowners; State and local government agencies; visitors to National
Forests, National Parks, and National Wildlife Refuges; and the general
public regarding the potential conservation value of the areas.
However, through the process of recognizing white fringeless orchid as
a candidate for Federal listing, much of this educational benefit has
already been realized and designating critical habitat would do little
to increase awareness about the species' presence and need for
conservation among affected land managers. Agencies, organizations, and
stakeholders are actively engaged in efforts to raise awareness for the
orchid and its conservation needs. For example, the Atlanta Botanical
Garden received a Five Star Urban Habitat Restoration grant to improve
habitat at several white fringeless orchid sites in Georgia, propagate
the species for reintroductions or augmentations, and establish
educational bog gardens at Chattahoochee Nature Center and the Atlanta
Botanical Garden. This project, which is separate from the USFS
agreement discussed above, involves seven official partners, including
two local high schools and Georgia State University. In addition,
designation of critical habitat could inform State agencies and local
governments about areas that could be conserved under State laws or
local ordinances. However, as awareness and education involving white
fringeless orchid is already well underway and the species currently
receives protection from adverse effects of management activities where
it occurs on public and privately owned conservation lands, designation
of critical habitat would likely provide only minimal incremental
benefits.
Increased Threat to the Species Outweighs the Benefits of Critical
Habitat Designation
Upon reviewing the available information, we have determined that
the designation of critical habitat would increase the threat to white
fringeless orchid from unauthorized collection and trade. At the same
time, designation of critical habitat is likely to confer little
measurable benefit to the species beyond that provided by listing.
Overall, the risk of increasing significant threats to the species by
publishing detailed location information in a critical habitat
designation greatly outweighs the benefits of designating critical
habitat.
In conclusion, we find that the designation of critical habitat is
not prudent, in accordance with 50 CFR 424.12(a)(1), because white
fringeless orchid is threatened by collection, and designation can
reasonably be expected to increase the degree of this threat to the
species and its habitat. However, we seek public comment on our
determination that designation of critical habitat is not prudent.
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened under the Act include recognition, recovery actions,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing results in public awareness, and
conservation by Federal, State, Tribal, and local agencies, private
organizations, and individuals. The Act encourages cooperation with the
States and other countries and calls for recovery actions to be carried
out for listed species. The protection required by Federal agencies and
the prohibitions against certain activities are discussed, in part,
below.
The primary purpose of the Act is the conservation of endangered
and threatened species and the ecosystems upon which they depend. The
ultimate goal of such conservation efforts is the recovery of these
listed species, so that they no longer need the protective measures of
the Act. Subsection 4(f) of the Act calls for the Service to develop
and implement recovery plans for the conservation of endangered and
threatened species. The recovery planning process involves the
identification of actions that are necessary to halt or reverse the
species' decline by addressing the threats to its survival and
recovery. The goal of this process is to restore listed species to a
point where they are secure, self-sustaining, and functioning
components of their ecosystems.
Recovery planning includes the development of a recovery outline
shortly after a species is listed and preparation of a draft and final
recovery plan. The recovery outline guides the immediate implementation
of urgent recovery actions and describes the process to be used to
develop a recovery plan. Revisions of the plan may be done to address
continuing or new threats to the species, as new substantive
information becomes available. The recovery plan also identifies
recovery criteria for review of when a species may be ready for
downlisting or delisting, and methods for monitoring recovery progress.
Recovery plans also establish a framework for agencies to coordinate
their recovery efforts and provide estimates of the cost of
implementing recovery tasks. Recovery teams (composed of species
experts, Federal and State agencies, nongovernmental organizations, and
stakeholders) are often established to develop recovery plans. If the
species is listed, the recovery outline, draft recovery plan, and the
final recovery plan, when completed, would be available on our Web site
(https://www.fws.gov/endangered), or from our Tennessee Ecological
Services Field Office (see FOR FURTHER INFORMATION CONTACT).
Implementation of recovery actions generally requires the
participation of a broad range of partners, including other
[[Page 55320]]
Federal agencies, States, Tribes, nongovernmental organizations,
businesses, and private landowners. Examples of recovery actions
include habitat restoration (e.g., restoration of native vegetation),
research, captive propagation and reintroduction, and outreach and
education. The recovery of many listed species cannot be accomplished
solely on Federal lands because their range may occur primarily or
solely on non-Federal lands. To achieve recovery of these species
requires cooperative conservation efforts on private, State, and Tribal
lands. If this species is listed, funding for recovery actions will be
available from a variety of sources, including Federal budgets, State
programs, and cost share grants for non-Federal landowners, the
academic community, and nongovernmental organizations. In addition,
pursuant to section 6 of the Act, the State(s) of Georgia, South
Carolina, and Tennessee and the Commonwealth of Kentucky would be
eligible for Federal funds to implement management actions that promote
the protection or recovery of the white fringeless orchid. Information
on our grant programs that are available to aid species recovery can be
found at: https://www.fws.gov/grants.
Although the white fringeless orchid is only proposed for listing
under the Act at this time, please let us know if you are interested in
participating in conservation efforts for this species. Additionally,
we invite you to submit any new information on this species whenever it
becomes available and any information you may have for conservation
planning purposes (see FOR FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is proposed or listed as an
endangered or threatened species and with respect to its critical
habitat, if any is designated. Regulations implementing this
interagency cooperation provision of the Act are codified at 50 CFR
part 402. Section 7(a)(4) of the Act requires Federal agencies to
confer with the Service on any action that is likely to jeopardize the
continued existence of a species proposed for listing or result in
destruction or adverse modification of proposed critical habitat. If a
species is listed subsequently, section 7(a)(2) of the Act requires
Federal agencies to ensure that activities they authorize, fund, or
carry out are not likely to jeopardize the continued existence of the
species or destroy or adversely modify its critical habitat. If a
Federal action may affect a listed species or its critical habitat, the
responsible Federal agency must enter into consultation with the
Service.
Federal agency actions within the species' habitat that may require
conference or consultation or both as described in the preceding
paragraph include management and any other landscape-altering
activities on Federal lands administered by the U.S. Fish and Wildlife
Service, USFS, and NPS; issuance of section 404 CWA permits by the
Corps; powerline right-of-way construction and maintenance by the
Tennessee Valley Authority; and construction and maintenance of roads
or highways by the Federal Highway Administration.
With respect to threatened plants, 50 CFR 17.71 provides that all
of the provisions at 50 CFR 17.61 shall apply to threatened plants.
These provisions make it illegal for any person subject to the
jurisdiction of the United States to import or export, transport in
interstate or foreign commerce in the course of a commercial activity,
sell or offer for sale in interstate or foreign commerce, or to remove
and reduce to possession any such plant species from areas under
Federal jurisdiction. In addition, the Act prohibits malicious damage
or destruction of any such species on any area under Federal
jurisdiction, and the removal, cutting, digging up, or damaging or
destroying of any such species on any other area in knowing violation
of any State law or regulation, or in the course of any violation of a
State criminal trespass law. However, there is the following exception
for threatened plants. Seeds of cultivated specimens of species treated
as threatened shall be exempt from all the provisions of 50 CFR 17.61,
provided that a statement that the seeds are of ``cultivated origin''
accompanies the seeds or their container during the course of any
activity otherwise subject to these regulations. Exceptions to these
prohibitions are outlined in 50 CFR 17.72.
We may issue permits to carry out otherwise prohibited activities
involving threatened plants under certain circumstances. Regulations
governing permits are codified at 50 CFR 17.72. With regard to
threatened plants, a permit issued under this section must be for one
of the following: Scientific purposes, the enhancement of the
propagation or survival of threatened species, economic hardship,
botanical or horticultural exhibition, educational purposes, or other
activities consistent with the purposes and policy of the Act.
It is our policy, as published in the Federal Register on July 1,
1994 (59 FR 34272), to identify to the maximum extent practicable at
the time a species is listed, those activities that would or would not
constitute a violation of section 9 of the Act. The intent of this
policy is to increase public awareness of the effect of a proposed
listing on proposed and ongoing activities within the range of species
proposed for listing.
Based on the best available information, the following activities
may potentially result in a violation of section 9 the Act; this list
is not comprehensive:
(1) Unauthorized collecting, handling, possessing, selling,
delivering, carrying, or transporting of white fringeless orchid,
including import or export across State lines and international
boundaries, except for properly documented antique specimens of this
species at least 100 years old, as defined by section 10(h)(1) of the
Act;
(2) Unauthorized removal, damage, or destruction of white
fringeless orchid plants from populations located on Federal land
(USFS, NPS, and Service lands); and
(3) Unauthorized removal, damage, or destruction of white
fringeless orchid plants on private land in violation of any State
regulation, including criminal trespass.
At this time, we are unable to identify specific activities that
would not be considered to result in a violation of section 9 of the
Act because white fringeless orchid occurs in a variety of habitat
conditions across its range and it is likely that site-specific
conservation measures may be needed for activities that may directly or
indirectly affect the species.
Questions regarding whether specific activities would constitute a
violation of section 9 of the Act should be directed to the Tennessee
Ecological Services Field Office (see FOR FURTHER INFORMATION CONTACT).
Required Determinations
Clarity of the Rule
We are required by Executive Orders 12866 and 12988 and by the
Presidential Memorandum of June 1, 1998, to write all rules in plain
language. This means that each rule we publish must:
(1) Be logically organized;
(2) Use the active voice to address readers directly;
(3) Use clear language rather than jargon;
(4) Be divided into short sections and sentences; and
(5) Use lists and tables wherever possible.
If you feel that we have not met these requirements, send us
comments by one
[[Page 55321]]
of the methods listed in the ADDRESSES section. To better help us
revise the rule, your comments should be as specific as possible. For
example, you should tell us the numbers of the sections or paragraphs
that are unclearly written, which sections or sentences are too long,
the sections where you feel lists or tables would be useful, etc.
National Environmental Policy Act
We have determined that environmental assessments and environmental
impact statements, as defined under the authority of the National
Environmental Policy Act (NEPA; 42 U.S.C. 4321 et seq.), need not be
prepared in connection with listing a species as an endangered or
threatened species under the Endangered Species Act. We published a
notice outlining our reasons for this determination in the Federal
Register on October 25, 1983 (48 FR 49244).
References Cited
A complete list of references cited in this rulemaking is available
on the Internet at https://www.regulations.gov and upon request from the
Tennessee Ecological Services Field Office (see FOR FURTHER INFORMATION
CONTACT).
Authors
The primary authors of this proposed rule are the staff members of
the Tennessee Ecological Services Field Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Transportation.
Proposed Regulation Promulgation
Accordingly, we propose to amend part 17, subchapter B of chapter
I, title 50 of the Code of Federal Regulations, as set forth below:
PART 17--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.
0
2. In Sec. 17.12(h), add an entry for Platanthera integrilabia (white
fringeless orchid) to the List of Endangered and Threatened Plants in
alphabetical order under FLOWERING PLANTS to read as follows:
Sec. 17.12 Endangered and threatened plants.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species
-------------------------------------------------------- Historic range Family Status When listed Critical Special
Scientific name Common name habitat rules
--------------------------------------------------------------------------------------------------------------------------------------------------------
Flowering Plants
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * * * *
Platanthera integrilabia......... White fringeless U.S.A. (AL, GA, KY, Orchidaceae........ T ........... NA NA
orchid. MS, NC, SC, TN).
* * * * * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * *
Dated: August 14, 2015.
Stephen Guertin,
Director, U.S. Fish and Wildlife Service.
[FR Doc. 2015-22973 Filed 9-14-15; 8:45 am]
BILLING CODE 4310-55-P