Endangered and Threatened Wildlife and Plants; Endangered Status for Agave eggersiana and Gonocalyx concolor, and Threatened Status for Varronia rupicola, 62560-62579 [2013-22742]
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62560
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Federal Register / Vol. 78, No. 204 / Tuesday, October 22, 2013 / Proposed Rules
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Dated: September 9, 2013.
Rachel Jacobson,
Principal Deputy Assistant Secretary for Fish
Wildlife and Parks.
[FR Doc. 2013–24169 Filed 10–3–13; 8:45 am]
BILLING CODE 4310–55–C
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R4–ES–2013–0103;
4500030113]
RIN 1018–AZ10
Endangered and Threatened Wildlife
and Plants; Endangered Status for
Agave eggersiana and Gonocalyx
concolor, and Threatened Status for
Varronia rupicola
Fish and Wildlife Service,
Interior.
ACTION: Proposed rule.
AGENCY:
tkelley on DSK3SPTVN1PROD with PROPOSALS
Executive Summary
We, the U.S. Fish and
Wildlife Service (Service), propose to
list Agave eggersiana (no common
name) and Gonocalyx concolor (no
common name) as endangered species,
and Varronia rupicola (no common
name) as a threatened species under the
Endangered Species Act of 1973, as
amended (Act). These three plants are
endemic to the Caribbean. The effect of
this regulation, if finalized, would be to
conserve A. eggersiana, G. concolor, and
V. rupicola under the Act.
DATES: We will accept comments
received or postmarked on or before
December 23, 2013. Comments
submitted electronically using the
Federal eRulemaking Portal (see
ADDRESSES section, below) must be
received by 11:59 p.m. Eastern Time on
the closing date. We must receive
requests for public hearings, in writing,
at the address shown in FOR FURTHER
INFORMATION CONTACT by December 6,
2013.
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–2013–0103, 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
SUMMARY:
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Processing, Attn: FWS–R4–ES–2013–
0103; Division of Policy and Directives
Management; U.S. Fish and Wildlife
Service; 4401 N. Fairfax Drive, MS
2042–PDM; Arlington, VA 22203.
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 the
Information Requested section below for
more information).
FOR FURTHER INFORMATION CONTACT:
Marelisa Rivera, Deputy Field
Supervisor, U.S. Fish and Wildlife
Service, Caribbean Ecological Services
Field Office, P.O. Box 491, Road 301
´
Km. 5.1, Boqueron, PR 00622; by
telephone 787–851–7297; or by
facsimile 787–851–7440. Persons who
use a telecommunications device for the
deaf (TDD) may call the Federal
Information Relay Service (FIRS) at
800–877–8339.
SUPPLEMENTARY INFORMATION:
Why we need to publish a rule. Under
the Act, if we intend to list a species as
endangered or threatened throughout all
or a significant portion of its range, we
are required to promptly publish a
proposal in the Federal Register and
make a final determination on our
proposal within 1 year. Listing a species
as an endangered or threatened species
can only be completed by issuing a rule.
Agave eggersiana, Gonocalyx concolor,
and Varronia rupicola are 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 proposal
has until now been precluded by other
higher priority listing activities.
This rule consists of a proposed rule
to list Agave eggersiana and Gonocalyx
concolor as endangered, and Varronia
rupicola as threatened. This proposed
rule reassesses all available information
regarding the status of and threats to A.
eggersiana, G. concolor, and V. rupicola.
Elsewhere in today’s Federal Register,
we propose to designate critical habitat
for A. eggersiana, G. concolor, and V.
rupicola under the Act.
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
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existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence.
We have determined that listing is
warranted for these species, which are
currently at risk throughout all of their
respective ranges due to threats related
to:
• A. eggersiana—potential future
development for residential, urban, and
tourist use; agriculture use; dropping of
debris; competing nonnative plants;
fires; predation; and disease cause by
insects (weevils).
• G. concolor—installation or
expansion of telecommunication towers,
road improvement, vegetation
management, and small number of
individuals and populations.
• V. rupicola—loss of habitat due to
urban development, right-of-way
development and maintenance,
deforestation, and hurricanes; and
inadequate existing regulatory
mechanisms (lack of enforcement).
We will seek peer review. We are
seeking comments from knowledgeable
individuals with scientific expertise to
review our analysis of the best available
science and application of that science
and to provide any additional
information to improve this proposed
rule. Because we will consider all
comments and information we receive
during the comment period, our final
determinations may differ from this
proposal.
Information Requested
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 biology, range, and population
trends of A. eggersiana, G. concolor, and
V. rupicola, including:
(a) Habitat requirements for feeding,
reproducing, and sheltering;
(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 these species, their habitat,
or both.
(2) The factors that are the basis for
making a listing determination for these
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Federal Register / Vol. 78, No. 204 / Tuesday, October 22, 2013 / Proposed Rules
species under section 4(a) of the Act,
which are:
(a) The present or threatened
destruction, modification, or
curtailment of their 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 their continued existence.
(3) Biological, commercial trade, or
other relevant data concerning any
threats (or lack thereof) to these species
and existing regulations that may be
addressing those threats.
(4) Additional information concerning
the historical and current status, range,
distribution, and population size of
these species, including the locations of
any additional populations of these
species.
(5) Any information on the biological
or ecological requirements of the species
and ongoing conservation measures for
the species and their habitats.
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
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. Please
include sufficient information with your
comments to allow us to verify any
scientific or commercial information
you include.
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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, Caribbean Ecological Services
Field Office (see FOR FURTHER
INFORMATION CONTACT).
Previous Federal Actions
Through February 1996
On December 15, 1980, Agave
eggersiana, Gonocalyx concolor, and
Varronia rupicola (as Cordia rupicola)
were identified as Category 2 candidate
species in the candidate notice of
review (CNOR) published in the Federal
Register (45 FR 82480). A Category 2
species was one for which the Service
had information that proposing as
endangered or threatened may be
appropriate but for which sufficient
information was not currently available
to support a proposed rule. None of the
three species was mentioned in the
November 28, 1983, CNOR (48 FR
53640), but all three again were named
as Category 2 candidate species in the
September 27, 1985, CNOR (50 FR
39526). They all remained Category 2
candidate species in the February 21,
1990 (55 FR 6184), and September 30,
1993 (58 FR 51144), CNORs.
Designation of Category 2 species was
discontinued in the February 28, 1996,
CNOR (61 FR 7596). The 1996 CNOR
redefined candidates to include only
species for which we have information
needed to propose them for listing, and
as a result, A. eggersiana, G. concolor,
and V. rupicola were removed from the
candidate list.
After February 1996: Agave eggersiana
On November 21, 1996, we received
a petition from the U.S. Virgin Islands
Department of Planning and Natural
Resources (DPNR) requesting that we
list Agave eggersiana as endangered. On
November 16, 1998, we published in the
Federal Register (63 FR 63659) our
finding that the petition to list A.
eggersiana presented substantial
information indicating that the
requested action may be warranted, and
we initiated a status review on the
plant.
On September 1, 2004, the Center for
Biological Diversity (CBD) filed a
lawsuit against the Department of the
Interior and the Service alleging that the
Service failed to publish a 12-month
finding for Agave eggersiana (Center for
Biological Diversity v. Norton, Civil
Action No. 1:04–CV–2553 CAP). In a
stipulated settlement agreement
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resolving that case, signed April 27,
2005, we agreed to submit our 12-month
finding for A. eggersiana to the Federal
Register by February 28, 2006. On
March 7, 2006, we published our 12month finding (71 FR 11367) that listing
of A. eggersiana was not warranted. On
September 9, 2008, CBD filed a
complaint that challenged our 12-month
finding (Center for Biological Diversity
v. Hamilton, Case No. 1:08–cv–02830–
CAP). In a settlement agreement
approved by the Court on August 21,
2009, the Service agreed to submit to the
Federal Register a new 12-month
finding for A. eggersiana. On September
22, 2010, we published in the Federal
Register (75 FR 57720) a finding that
listing A. eggersiana was warranted, but
precluded by higher priority actions to
amend the Lists of Endangered and
Threatened Wildlife and Plants.
Agave eggersiana was named a
candidate species with a listing priority
number (LPN) of 8 in the CNORs
published on November 10, 2010 (75 FR
69222), October 26, 2011 (76 FR 66370),
and November 21, 2012 (77 FR 69993).
An LPN of 8 was assigned to Agave
eggersiana because the species faced
threats of moderate magnitude that were
imminent.
After February 1996: Gonocalyx
concolor and Varronia rupicola
On October 25, 1999, we published in
the Federal Register a CNOR (64 FR
57535) that added Gonocalyx concolor
and Varronia rupicola (as Cordia
rupicola) to the list of candidate species
with LPNs of 5 and 2, respectively.
Gonocalyx concolor was assigned an
LPN of 5 because it faced threats that
were high in magnitude but
nonimminent. Varronia rupicola (as
Cordia rupicola) was assigned an LPN of
2 because it faced threats of a high
magnitude that were imminent. These
two plants retained their respective LPN
assignments in the CNORs published 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),
and September 12, 2006 (71 FR 53756).
In the CNOR published on December
6, 2007 (72 FR 69034), Varronia
rupicola (as Cordia rupicola) was
assigned an LPN of 5, because its threats
were determined to be nonimminent. In
the 2007 CNOR, Gonocalyx concolor
retained its LPN of 5. Both plants
retained an LPN of 5 in the CNORs
published on December 10, 2008 (73 FR
75176), November 9, 2009 (74 FR
57804), November 10, 2010 (75 FR
69222), October 26, 2011 (76 FR 66370),
and November 21, 2012 (77 FR 69993).
On May 11, 2004, we received a
petition from the CBD (CBD 2004, pp.
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66–69) requesting that G. concolor and
V. rupicola be listed as an endangered
species under the Act. No new
information was provided in the
petition.
Species Information
Taxonomy and Description
tkelley on DSK3SPTVN1PROD with PROPOSALS
Agave eggersiana
Agave eggersiana is a flowering plant
of the family Agavaceae (century plant
family) endemic to the island of St.
Croix in the U.S. Virgin Islands (USVI).
This species was originally described in
1913, by William Trelease from material
collected on St. Croix, and is
distinguished from other members of
the Agavaceae family by its acaulescent
(without an evident leafy stem), nonsuckering growth habit (vegetative
reproduction that does not form
offshoots around its base), and its
fleshy, nearly straight leaves with small
marginal prickles of 0.04 inches (in) (0.1
centimeters (cm)) long that are nearly
straight (Britton and Wilson 1923, p.
´
156; Proctor and Acevedo-Rodrıguez
2005, p. 118). Its flowers are deep
yellow and 2.0 to 2.34 in (5 to 6 cm)
long. After flowering, the panicles
(inflorescence) produce numerous small
vegetative bulbs (bulbils), from which
the species can be propagated (Proctor
´
and Acevedo-Rodrıguez 2005, p. 118).
Agave eggersiana is not known to
produce fruit, and like other Agave
species, is monocarpic, meaning the
plant dies after producing the spike or
inflorescence. Furthermore, based on
observations of cultivated plants, A.
eggersiana requires at least 10 to 15
years to develop as a mature individual
and to produce an inflorescence (David
Hamada, St. George Village Botanical
Garden, pers. comm., 2010).
Gonocalyx concolor
Gonocalyx concolor was described in
1970, as a new species of the genus
Gonocalyx, family Ericaceae, for Puerto
Rico (Nevling 1970, p. 221). Gonocalyx
is a neotropical genus comprised of 10
species, ranging from Costa Rica to
North Colombia, and the Caribbean
(Dominican Republic, Puerto Rico,
Dominica, and Guadalupe) (Luteyn and
˜
Pedraza-Penalosa 2011, p. 1). Two of the
species are considered endemic to
Puerto Rico: G. concolor and G.
portoricensis (Lioger and Martorell
2000, p. 151). These two species are
derived from common ancestral stock;
hence there is great similarity in many
details and in aspect, as well as
geographic proximity (Nevling 1970, p.
223).
Although G. concolor is similar to G.
portoricensis, differences in distribution
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and flower morphology indicate that
they are well-differentiated species
(Nevling 1970, p. 224). The flower of G.
portoricensis is pendent with light green
calyx, and the corolla tube is whitish to
pinkish; G. portoricensis is insectpollinated flower (Proctor 1992, p. 3).
Gonocalyx concolor differs from G.
portoricensis in its vivid red,
semipendent flowers, which apparently
are hummingbird pollinated, and in its
range (Nevling 1970, p. 224). Gonocalyx
concolor is a small evergreen shrub,
mainly epiphytic (grow on the trunks of
trees) or clambering (use other
vegetation as support), which may reach
15 feet (ft) (4.7 meters (m)) in length
(Acevedo 2005, p. 227). The leaves are
simple, alternate, entire, and coriaceous
(leathery). The leaf blade is ovate,
broadly elliptic, or nearly orbicular; 0.5
to 1.2 in (1.5 to 3 cm) long; and 0.5 to
0.9 in (1.3 to 2.3 cm) broad. The leaf
base is apiculate (ending in a short
sharp point) and obtuse to acute at the
apex, and is rounded at the base; the
leaf’s upper surface is glabrous (smooth
or hairless) above, with scattered large
trichomes (papilliform hairs) beneath.
The leaf venation is 5-pli (the leaf
venation is 1 central vein and 4
secondary veins bending toward apex)
from the base (secondary veins bending
toward apex), outer set marginal, inner
set submarginal and better developed.
The mid-vein is immersed above and
emerged beneath, and lateral venation is
inconspicuous. The leaf margin is entire
or flat, except for few inconspicuous,
rounded projections toward the apex.
The leaf lower surface is pale green and
shiny. The petiole (the stalk attaching
the leaf blade to the stem) is
approximately 0.07 to 0.09 in (0.18 to
0.21 cm) long. The stems are highly
branched, slender, cylindrical, and dark
brown in color. The twigs are pubescent
(covered with fine short hairs). Young
leaves and branches are brilliantly rosecolored, but become green with age.
Flowers are bisexual, 5-merous (floral
part in multiples of 5 in each whorl),
regular, and uniformly vivid red.
Flowers are borne solitary on auxillary
brachyblast (short shoot), and are
semipendent (hanging or suspended).
Pedicel is terete (cylindrical and
tapering), 0.35 to 0.43 in (0.89 to 1.1 cm)
long, red, fringed with trichomes at the
summit, bibracteolate (2 bracts
subtending the flower within an
inflorescence) near the base, and
articulate with calyx. The corolla (the
part of a flower that consists of the
separate or fused petals and constitutes
the inner whorl of the perianth) tube is
carnose (of a fleshy consistence),
campanulate (shape like a bell), and
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about 0.5 to 0.6 in (1.3 to 1.5 cm) in
length and 0.2 to 0.3 in (0.5 cm to 0.8
cm) in diameter.
Fruit is a bright red berry with many
seeds inside (Lioger 1995, p. 105). No
additional information regarding fruit
production is available.
Varronia rupicola
Varronia was traditionally lumped
into the genus Cordia, a group of about
250 or more species of trees and shrubs
of tropical and subtropical regions.
Varronia was recently recognized as a
monophyletic genera based on
vegetative, floral, and pollen
morphology (Miller and Gottschling
2007, p. 163). Varronia comprises multistemmed shrubs with condensed
inflorescence and evenly serrate leaves
´
(Sanchez de Stapf 2010, p. 133).
Varronia is currently represented in the
West Indies by about 66 valid species
´
(Acevedo-Rodrıguez and Strong 2012, p.
170). Axelrod (2011, p. 427) recognized
seven species found in Puerto Rico,
with V. bellonis and V. wagnerorum
being endemic to the island, and V.
rupicola extending to the island of
Anegada, British Virgin Islands.
Varronia rupicola is a large shrub
reaching up to 16 ft (5 m) in height. The
alternate leaves are ovate to elliptic, 0.8
to 3.5 in (2 to 9 cm) long with an acute
apex, rounded to obtuse at the base, and
chartaceous (papery). Leaves margins
are whole or crenate (scalloped or
notched). The upper surface of the leaf
is rigidly scabrous (having a rough
surface) and puberulous (densely
covered by hairs) underneath, with
strigose (having straight hairs) petioles
ranging from 0.1 to 0.4 in (0.2 to 1.0 cm)
long. Flowers are in solitary globular
heads of 20 (grouped into a globose
terminal structure), and about 0.4 in (1.0
cm) in diameter. The corolla is white
and 0.3 in (0.8 cm) long, and the fruit
is a one-seeded, red drupe about 0.2 in
(0.5 cm) long (Proctor 1991, p. 65;
Lioger 1995, p. 313).
Habitat
Agave eggersiana
Agave eggersiana is currently known
from coastal cliffs with sparse
vegetation and dry coastal shrubland
vegetation communities within the
subtropical dry forest life zone of St.
Croix, USVI (Ewel and Whitmore 1973,
p. 72). In St. Croix, the average rainfall
is about 30 in (76 cm) and 40 in (102
cm) in the east and west sides of the
island, respectively (Ewel and
Whitmore 1973 p. 8; Mac et al. 1998, p.
315). The wettest and hottest months are
from July to October. The average mid
island temperature is 78.8 degrees
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Fahrenheit (°F) (26 degrees Celsius (°C),
with a variation of only 5 to 9 °F (3 to
5 °C) between the warmest and coolest
months (Mac et al. 1998, p. 316).
The coastal cliffs where Agave
eggersiana occurs are dominated by
rocky formations and areas with less
than 10 percent vegetative cover. These
coastal cliffs are exposed to extremes of
wind, salt spray, and low moisture, and
they are usually sparsely vegetated with
a canopy less than 1 meter in height
(Gibney et al. 2000, p. 7; Moser et al.
2010, Appendix A–11). Dry coastal
shrubland vegetation is common to the
drier parts of the island of St. Croix: east
and south shores, and low-elevation
locations. In some places, dry coastal
shrubland vegetation may extend as far
up as 902 ft (275 m) on south-facing
slopes. Cacti and agave are common
though scattered, while vegetation
height can range from 3.2 to 32.8 ft (1
to 10 m). The taller forms may consist
of a canopy layer of larger individuals
under slightly more moist conditions.
The shorter forms are common to very
exposed locations such as the east sides
of headlands on the south shores in the
island (Gibney et al. 2000, p. 6; Moser
et al. 2010, Appendix A–8). Other
species of vegetation associated with
these areas are: Sesuvium
portulacastrum (sea purslane),
Laguncularia racemosa (white
mangrove), Bucida buceras (black olive),
Hippomane mancinella (manchineel),
Jacquinia arborea (barbasco), Opuntia
stricta (prickly pear, Pilosocereus
royenii (Royen’s tree, Suriana maritima
(bay cedar), Bursera simaruba (gumbo
limbo, Canavalia rosea (seaside bean),
Caesalpinia bonduc (gray nicker),
Capparis flexuosa (falseteeth), Scaevola
plumieri (ink berry), Oplonia spinosa
(prickly bush), Capparis indica
(linguam), Adelia ricinella (wild lime),
Crossopetalum rhacoma (maidenberry,
Heteropterys purpurea (bull withe),
Pisonia subcordata (mampoo),
Exostema caribaeum (Caribbean
princewood, Cordia dentata (white
manjack), and Coccoloba uvifera
(seagrape) (O. Monsegur and M. Vargas,
Service, unpubl. data 2013; Lioger and
Martorell 2000, pp. 50–205).
The natural populations of Agave
eggesiana grow on top of various soil
classifications, including Cramer,
Glynn, Hasselberg, Southgate, and
Victory. The Cramer and Southgate
series consists of shallow, well-drained
soils on summits and side slopes of
volcanic hills and mountains. These
soils formed in material weathered from
extrusive igneous bedrock or only from
igneous bedrock. The Hesselberg series
consists of shallow, well-drained soils
on marine terraces. These soils formed
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in alkaline, clay sediments. The Glynn
series consists of very deep, welldrained soils on alluvial fans and
terraces. These soils formed in stratified
alluvial sediments weathered from basic
igneous rock. The Victory series consists
of moderately deep, well-drained soils
on summits and side slopes of volcanic
hills and mountains. These soils formed
in material weathered from extrusive
igneous bedrock (USDA–NRCS 2013,
https://websoilsurvey.nrcs.usda.gov).
Gonocalyx concolor
Gonocalyx concolor has been
described as endemic from the elfin
forest type at Cerro La Santa and from
the ausubo (Manilkara bidentata) forest
type at Charco Azul, both within the
lower montane (an altitudinal zone in
mountainous region characterized by
distinctive flora and forest structure)
very wet forest life zone in the Carite
Commonwealth Forest (Ewel and
Whitmore 1973, p. 41). The Carite
Commonwealth Forest comprises
approximately 6,694.9 acres (ac)
(2,709.3 hectares (ha)), and the elevation
ranges from 2,030 to 3,950 ft (620 to 900
m) (DNR 1976, p. 169). This forest has
been managed for conservation since
1975 (DNER 2008, p. 1). The mean
annual precipitation at the Carite
Commonwealth Forest is 88.7 in (225
cm), with February to April the drier
months (NOAA 2013, https://
www.srh.noaa.gov/sju/?n=climo_cayey).
The mean temperature is 22.7 °C (72.3
°F), varying from 20 °C (68 °F) in
January to 24 °C (73.4 °F) in July
(Silander et al. 1986, p. 183).
Both the elfin and ausubo forests have
similar climate conditions (Ewel and
Whitmore 1973, p. 32). The elfin forest,
also referred to as dwarf or cloud-forest,
is found on exposed peaks and ridges of
Cerro La Santa, above 2,890 ft (880 m)
in elevation from sea level, occupying
approximately 10.1 ha (24.9 ac) in the
Carite Commonwealth Forest (Silander
et al. 1986, p. 178). The elfin forest
vegetation is characterized by gnarled
trees less than 7 meters tall, high basal
area, small diameters, a large number of
stems per unit area, and extremely slow
growth rates (Ewel and Whitmore 1973,
p. 45). The vegetation is commonly
saturated with moisture and frequently
enveloped in clouds, and both aerial
and superficial roots are common
(Weaver et al. 1986, p. 79). The plant
association in this area is generally
comprised by few species of native
trees, native ferns and dense covered
with epiphytes including bromeliads
and mosses (Weaver et al. 1986, p. 79).
The native tree composition includes:
Tabebuia schumanniana (roble
colorado), Tabebuia rigida (roble de
PO 00000
Frm 00092
Fmt 4702
Sfmt 4702
62563
sierra), Ocotea spathulata (nemoca
cimarrona), Eugenia borinquensis
(guayabota), Clusia minor (cupey de
monte), and Prestoea acuminata var.
montana (sierra palm) (Weaver et al.
1986, p. 80; Silander et al. 1986, p. 191).
Additionally, some areas were planted
with Eucalyptus robusta (swamp
mahogany) (O. Monsegur, UPRM,
unpubl. report, 2006, p. 1).
The ausubo forest is only found along
´
the Rıo Grande de Patillas River basin
and intermittent streams between 2,034
ft (620 m) and 2,329.4 ft (720 m) of
elevation (DNR 1976, p. 169), and
occupying approximately 72.5 ha (179.2
ac) in the Charco Azul area (Silander et
al. 1986, p. 190). The ausubo forest is
characterized by evergreen vegetation,
high species richness, rapid growth rate
of successional trees, epiphytic ferns,
bromeliads, and orchids (Ewel and
Whitmore 1973, p. 32). The vegetation
in this area is generally comprised of
native trees (i.e., Manilkara bidentata
(ausubo), Dacryodes excelsa (tabonuco),
Guarea guidonia (guaraguao), and
Cyrilla racemiflora (swamp titi) (Francis
and Lowe 2000, p. 345; DNER 2008, p.
2). Gonocalyx concolor grows epiphytic
and clambering on dead and live stand
trees within this type of forest (O.
Monsegur, UPRM, unpubl. report, 2006,
p. 2).
Varronia rupicola
Varronia rupicola has been described
from southwestern Puerto Rico, Vieques
Island, and Anegada Island. All these
sites lie within the subtropical dry forest
life zone overlying a limestone substrate
(Ewel and Whitmore 1973, p. 72).
Subtropical dry forest life zones receive
a mean annual rainfall ranging from 24
to 40 in (61 to 101 cm). The vegetation
in this life zone is deciduous on most
soils, with tree species dropping leaves
during the dry season. The vegetation
usually consists of a nearly continuous,
single-layered canopy, with little
ground cover. The leaves of dry forest
species are succulent or coriaceous, and
species with spines and thorns are
common. Tree heights usually do not
exceed 49 ft (15 m), and crowns are
typically broad, spreading, and flattened
(Ewel and Whitmore 1973, p. 72).
Varronia rupicola has been recorded
in forested hills with open to relatively
dense shrublands and scrublands 6.5 to
9.8 ft (2 to 3 m) in height; in low forest
with canopy from 8 to 15 ft (3 to 5 m)
high; and at the edge of a dense, low
coastal shrubland forest. On the island
of Anegada, V. rupicola was found in
open limestone pavement and sand
dunes. Woody species associated to V.
rupicola’s prime habitat in southern
´
Puerto Rico (Guanica Commonwealth
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Forest) include: Gymnanthes lucida
´
(shiny oysterwood, or yaitı), Exostema
caribaeum (princewood, or albarillo),
Pisonia albida (corcho), Pictetia
aculeata (fustic, or tachuelo), Thouinia
portoricensis (ceboruquillo, or
serrazuela), Coccoloba krugii
(whitewood), Pilosocereus royenii
´
(Royen’s tree cactus, or sebucan),
Bursera simaruba (gumbo limbo, or
almacigo), Erithalis fruticosa (black
torch), Guettarda krugii (frogwood, or
cucubano), Tabebuia heterophylla (pink
trumpet tree, or roble), Hypelate
trifoliata (inkwood), Coccoloba
diversifolia (pigeonplum, or uvilla),
Cassine xylocarpa (marbletree, or
´
coscorron), Krugiodendron ferreum
(black ironwood, or palo de hierro),
Jacquinia berterii (barkwood), Bourreria
succulenta (strongbark, or palo de vaca),
Crossopetalum rhacoma (maidenberry,
or pico de paloma), Antirhea acutata
(placa chiquitu, or quina), and Amyris
elemifera (torchwood) (Murphy and
Lugo 1986, p. 91). The populations of V.
rupicola in Puerto Rico are also found
in close proximity to populations of the
endangered plants Eugenia
woodburyana (no common name) and
Trichilia triacantha (bariaco), and other
rare plants such as Myrtus bellonis (no
common name), Passiflora bilobata
(twolobe passionflower), and Nashia
inaguensis (pineapple verbena)
(Breckon and Kolterman 1996, p. 4;
Monsegur and Breckon 2007, p. 1). On
Anegada, the species is located in open
limestone pavement and sand dunes. In
a comprehensive study of the vegetation
of Anegada, V. rupicola was found in
higher abundance (based on percentage
occurrence across plots) on limestone
but also widespread within the sand
dunes (Clubbe et al. 2004, p. 344).
Occurrence of the species on sand
dunes on Anegada may explain the new
record of the species in the northern
coast (Tortuguero Lagoon) of Puerto
Rico within an area that is characterized
by the presence of white sands soils (O.
Monsegur, Service, pers. obs., 2013).
tkelley on DSK3SPTVN1PROD with PROPOSALS
Life History
Agave eggersiana
Based on the information currently
available to us, there is no published
information describing the ecology and
genetics of Agave eggersiana. Although
samples from individuals in the Gallows
Bay area have been collected for genetic
analysis (Ray, VFR, pers. comm., 2010),
the Service is unaware if the samples
were analyzed and results have been
published. No further information is
available regarding the ecology of the
species beyond the demographic trends
discussed above.
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Gonocalyx concolor
Gonocalyx concolor has been
observed flowering in December,
January, February, and April (Nevling
1970, p. 224). Preliminary studies of the
species’ reproductive biology indicate
that the plant is predominantly
outcrossed, and that outcrossed flowers
produce twice the number of seeds than
self-pollinated flowers (S. Flores,
Universidad del Turabo, pers. comm.
1996). The low number of individuals
per population may suggest that
Gonocalyx concolor has highly
specialized ecological requirements to
grow and that production of viable
seeds rarely occurs (C. Pacheco, Service,
pers. obs., 2013). Although a number of
authors have reported the species on
flower and fruit, no one has observed
recruitment. Currently, no information
about reproductive capacity, dispersion,
or habitat requirements is available for
G. concolor.
Varronia rupicola
Studies on the distribution,
abundance, and reproductive biology of
Varronia rupicola have been conducted
by scientists from the University of
¨
Puerto Rico, Mayaguez Campus
(Breckon and Kolterman 1996, p. 6;
Monsegur and Breckon 2007, p. 13).
These authors reported the species
flowering and fruiting in December
through January (Breckon and
Kolterman 1996, p. 4), and in June
through July (Monsegur and Breckon
2007, p. 1). From February to April, all
plants observed were sterile. Fruit
production in the populations from the
´
Guanica Commonwealth Forest and the
municipality of Ponce seem to be high,
and there is evidence of recruitment
associated to the majority of the clusters
of individuals (O. Monsegur, Service,
pers. obs., 2013). Under greenhouse
conditions, seed germination has been
reported as not less than 67 percent
(Wenger et al. 2010). Germination in the
wild has also been observed to be high
(O. Monsegur, Service, pers. obs., 2013).
However, apparently there is also a high
mortality of seedlings, and only few
individuals make the transition (natural
thinning) to sapling stages (O.
Monsegur, Service, pers. obs., 2013).
Monsegur and Breckon (2007, p. 2)
reported numerous seedlings (>140) and
´
various saplings in the Guanica
Commonwealth Forest. However,
seedling recruitment on Vieques Island
seems to be low, as it has not been
recorded during recent assessments
(Monsegur and Breckon 2007, p. 7;
Hamilton, KEW, pers. comm., 2013).
Despite the showy red fruits of Varronia
rupicola, its dispersion seems to be
PO 00000
Frm 00093
Fmt 4702
Sfmt 4702
almost limited by gravity, as the
majority of the seedlings lie under the
parent tree or downslope (O. Monsegur,
Service, pers. obs. 2013). The wide
range of the species suggests a former
animal disperser (probably a bird).
Patterns of plant-animal interactions
were probably altered due to the
previous extensive deforestation of the
island of Puerto Rico. Some
observations of seed dispersal by an
undetermined vector have been reported
from Anegada (Hamilton, KEW, pers.
comm., 2013). If not extinct, possible
dispersers may have altered their
foraging behavior and now do not feed
on the fruits of V. rupicola. Recent
observations in Puerto Rico indicate that
flowers of V. rupicola are visited by
several insect species, including Apis
mellifera (honey bee) and
Electrostrymon angelia (fulvous
hairstreak, a butterfly) (O. Monsegur,
Service, pers. obs. 2013).
Varronia rupicola material
germinated in the greenhouse at Cabo
Rojo National Wildlife Refuge in Cabo
Rojo were flowering and producing
fruits in about 1 year after germination
(O. Monsegur, Service, pers. obs., 2013).
The rapid reproductive development of
the species and the finding of
individuals along recently disturbed
sites (new dirt roads) and natural forest
gaps (openings) may indicate that V.
rupicola is an early colonizer or pioneer
species.
Historical Range
Agave eggersiana
Historically, Agave eggersiana was
reported from the north coast in
Christiansted, St. Croix, and along the
south coast of the island (Proctor and
´
Acevedo-Rodrıguez 2005, p. 118).
Britton and Wilson (1923, p. 156)
reported the species from hillsides and
plains in the eastern dry districts of St.
Croix, but did not provide population
estimates. In addition, it was reported
that A. eggersiana was cultivated on St.
Croix and St. Thomas for ornament
(Trelease 1913, p. 28; Britton and
Wilson 1923, p. 156; Proctor and
´
Acevedo-Rodrıguez 2005, p. 118).
Information provided (Kojis and
Boulon, DPNR, pers. comm., 1996)
specified that the species was last
observed growing in the wild around
1984 to 1986 on St. Croix. In 2003,
DPNR stated that the species was
believed to be extinct (Plaskett, DPNR,
pers. comm. 2003; Dalmida-Smith,
DPNR, pers. comm., 2010). Proctor and
´
Acevedo-Rodrıguez (2005, p. 118)
provided a general description of A.
eggersiana and state that the species
appeared to be extinct in the wild.
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However, no citations or survey
information were provided to support
this statement. Subsequently, in 2010,
DPNR provided information based on
field visits and reported the existence of
several populations of A. eggersiana on
St. Croix (Dalmida-Smith, DPNR, pers.
comm., 2010).
Historically, land use intensity
increased by colonial exploitation since
the 15th century (Chakroff 2010, p. 6).
Sugarcane was the main crop on the
island and dominated the economy for
nearly 200 years (Shaw 1933, p. 414).
Apparently, the former land use of the
areas used for sugar cane cultivation
resulted in degradation of the species’
habitat and nearly extirpated the species
from the wild. Sugarcane is no longer
cultivated commercially on the island,
the majority of the areas formerly used
for sugarcane plantations are currently
grasslands, and early secondary forests
are dominated by the nonnative tree
Leucaena leucocephala (white leadtree).
Gonocalyx concolor
Gonocalyx concolor was first
discovered on Cerro La Santa at an
elevation of approximately 2,962 ft (903
m) in the Carite Commonwealth Forest,
east-central Puerto Rico (Nevling 1970,
p. 221). In 1993, Dr. Frank Axelrod
found a second population of this
species close to the Charco Azul
recreational area, also in the Carite
Commonwealth Forest (Axelrod 1993,
UPR herbarium voucher 6643). This
population is located at an approximate
elevation of 2,070 ft (630 m) in the
ausubo forest, which lies within the
´
basin of the Rıo Grande de Patillas,
approximately 2 mi (3.2 km) southeast
from Cerro La Santa. Later, in December
2006, Omar Monsegur (former student
from the University of Puerto Rico)
visited the known localities describing
three populations of Gonocalyx
concolor in the Carite Commonwealth
Forest: two at Cerro La Santa, and
another at Charco Azul (O. Monsegur,
UPRM, unpubl. report, 2006, p.1). Dr.
Samuel Flores (pers. comm., 1996),
professor at the Turabo University in
Puerto Rico, anecdotally reported the
species from El Yunque National Forest
in the Luquillo Mountains, northeastern
Puerto Rico. Despite of Service efforts to
locate the species in El Yunque National
Forest, it has not been found. Therefore,
this record has not been confirmed.
DNER, pers. comm., 2004). In 2005, an
individual of V. rupicola was found on
Lighthouse Peninsula, Vieques Island
(Breckon and Kolterman 2005, p. 1).
This area is located within the Vieques
Island National Wildlife Refuge.
Current Range
Agave eggersiana
Varronia rupicola
Varronia rupicola was first discovered
by the German botanical collector Paul
Sintenis in July 1886, in the Los Indios
Ward, located between the Barinas ward
in Yauco and the municipality of
Guayanilla, Puerto Rico. It was later
´
found in Guanica, Puerto Rico, in 1887,
and again in 1943 and 1959 (Proctor
1991, p. 66). The species was thought to
be endemic to Puerto Rico, until it was
collected by George Proctor in May
1987, at the west end of the island of
Anegada, British Virgin Islands (Proctor
1991, p. 66). Proctor (1994, p. 54) also
´
reported a specimen from Punta Jalova
on Vieques Island, Puerto Rico. This
report was based on a specimen
collected by Woodbury, possibly around
1978. Surveys conducted by Breckon
and Kolterman in 1995 located the
˜´
species at a site called El Penon in the
˜
municipality of Penuelas (Breckon and
Kolterman 1996, p. 6). In 2003, three
individuals of V. rupicola were found
adjacent to the entrance of El Fuerte
´
Trail within the Guanica
Commonwealth Forest (M. Canals,
Agave eggersiana is currently found
on the north and south coasts of St.
Croix, USVI. Seven populations support
approximately 313 adult plants and
more than 316 juveniles. It is uncertain
if these populations are natural
(individuals that come from wild
populations) or if these populations
consist of individuals that escaped from
landscaping. However, characteristics,
such as growing mixed with native
vegetation, evidence of natural
recruitment, and the presence of
different size classes, suggest these are
remnants of wild populations.
The current distribution of
populations of Agave eggersiana on St.
Croix that are presumed to be wild is as
follows:
a. North coast—(1) Gallows Bay with
an estimate of 2 individuals; and (2)
Protestant Cay with an estimated 40
individuals.
b. South coast—(3) Manchenil Bay
with an estimated 8 individuals; (4)
West side of Vagthus point with a single
individual; (5) Great Pond with
approximately 65 individuals; (6) South
Shore with an estimate of 182
individuals; and (7) Cane Garden Bay
with 15 individuals.
Most of the sites have juvenile
individuals except for Gallows Bay and
Vagthus Point (Table 1).
TABLE 1—(PRESUMED) WILD POPULATIONS OF AGAVE EGGERSIANA
Area/
location
Population
Ownership
182/231
15/27
8/58
40/Undetermined
313/316+
South Shore ..........................
Cane Garden Bay .................
Manchenil Bay .......................
Protestant Cay .......................
South Coast
South Coast
South Coast
North Coast
..........................
..........................
..........................
..........................
Cane Garden ........................
Cane Garden ........................
Granard .................................
Protestant Cay ......................
Gallows Bay ..........................
West Vagthus Point ...............
Great Pond ............................
North Coast ..........................
South Coast ..........................
South Coast ..........................
Mount Welcome ....................
Peters Minde ........................
Great Pond ...........................
Private ...................................
Private ...................................
Private ...................................
Government but leased to
private party.
Private ...................................
Private ...................................
Government ..........................
Total ...............................
tkelley on DSK3SPTVN1PROD with PROPOSALS
Number of
individuals
(adults/juveniles)
Estate
...............................................
...............................................
...............................................
2/0
1/0
65/Undetermined
Sources: O. Monsegur and M. Vargas, Service, unpubl. data, 2010 and 2013; Dalmida- Smith, DPNR, pers. comm., 2010; David Hamada,
SGVBG, pers. comm., 2010; Plaskett, DPNR, pers. comm., 2003.
In addition, there are introduced
individuals located at Salt River
National Park and Ecological Preserve
(SARI) with an estimate of 90
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Jkt 232001
individuals (mostly juveniles); Buck
Island National Monument with an
estimate of 11 individuals; and Ruth
Island with 1 individual (O. Monsegur
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Sfmt 4702
and M. Vargas, Service, pers. obs., 2010
and 2013; Dalmita-Smith, DPNR, pers.
comm., 2010).
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Gonocalyx concolor
Currently, Gonocalyx concolor is
known from three populations: two at
Cerro La Santa and another at Charco
Azul, both in the Carite Commonwealth
Forest (Pacheco and Monsegur, Service,
unpubl. report, 2013, p. 2). The species
shows a limited distribution in its
habitat, occupying only 0.75 ac (0.3 ha)
at Cerro La Santa (Pacheco and
Monsegur Service, unpubl. report, 2013,
p. 3) and approximately 0.12 ac (0.05
ha) at Charco Azul (O. Monsegur,
UPRM, unpubl. report, 2006, p.2). The
individuals reported from El Yunque
National Forest are apparently no longer
extant. According to Luis Rivera,
Tropical Vegetation Specialist, the U.S.
Forest Service does not have records of
the species in El Yunque National
Forest (L. Rivera, USFS, pers. comm.,
2013). Despite the availability of habitat,
the Service considers that the report
from El Yunque National Forest may be
a misidentification of material from G.
portoricensis.
In 1992, Dr. George R. Proctor
conducted a status review of the species
estimating its population at Cerro La
Santa at around 35 individuals (Proctor
1992, p. 4). Later, Dr. Samuel Flores
(professor from the Turabo University)
visited the same area and estimated its
population at around 172 individuals
(S. Flores, pers. comm., 2009). In
December 2006, Omar Monsegur
(graduate student from the University of
¨
Puerto Rico, Mayaguez Campus)
estimated approximately 25 individuals
at Cerro La Santa and 4 individuals at
Charco Azul (O. Monsegur, UPRM,
unpubl. report, 2006, p. 1). In 2013,
Service biologists, Carlos Pacheco and
Omar Monsegur, visited the population
at Cerro La Santa and estimated the G.
concolor population at around 27
individuals (Pacheco and Monsegur,
USFWS, unpubl. report, 2013, p. 3).
Varronia rupicola
Varronia rupicola is currently known
from at least seven main localities in
Puerto Rico (Table 2) and several
localities from the island of Anegada.
Monsegur and Breckon (2007, p. 1)
visited the historical localities in Puerto
Rico and provided updated information
about the status and distribution of the
species. The distribution of V. rupicola
´
in the Guanica Commonwealth Forest
extents to at least six small populations
or subpopulations within the east
section of the forest. Another population
was located on the west unit of the
´
Guanica Commonwealth Forest by
Alcides Morales (Sociedad Ornitologica
˜
Puertoriquena, Inc., pers. comm., 2012).
This is the westernmost recorded
distribution for the species.
˜
From the municipality of Penuelas,
Monsegur and Breckon (2007, p. 6)
found a single individual in a ravine
˜´
area on the west side of El Penon site.
This seems to be part of the same
population identified by Breckon and
Kolterman in 1995. In addition, the
Service confirmed the presence of about
eight clusters of the species in an area
just north of the Ponce Holiday Inn in
the municipality of Ponce (O. Monsegur,
Service, and J. Sustache, DNER, unpubl.
Data, 2013).
TABLE 2—STATUS OF CURRENTLY KNOWN POPULATIONS OF VARRONIA RUPICOLA
Number of
reproductive
individuals
Localities
Number of
saplings
Number of
seedlings
Total of plants
16
34
1
6
2
17
1
0
30
0
0
0
4
0
0
142
0
0
0
120
0
16
206
1
6
2
141
1
Total ..........................................................................................................
tkelley on DSK3SPTVN1PROD with PROPOSALS
˜´
˜
El Penon (Penuelas) ........................................................................................
´
Guanica Commonwealth Forest (East) ...........................................................
´
Guanica Commonwealth Forest (West) (Montalva) ........................................
Puerto Ferro (Vieques NWR) ..........................................................................
Yauco (Montes de Barina) ...............................................................................
Ponce (Holiday Inn) .........................................................................................
Tortuguero Lagoon (DNER) ............................................................................
77
34
262
373
Another recorded site for Varronia
rupicola lies within a privately owned
property located at Montes de Barinas in
the municipality of Yauco (C. Pacheco,
Service, pers. comm., 2011). The species
was also reported by Alcides Morales
˜
(Sociedad Ornitologica Puertoriquena,
Inc., pers. comm., 2012) from a nearby
´
property known as Finca Catala. This
property is adjacent to the locality
reported by Pacheco on 2011. These
reports overlap with the general area
where this specimen was collected by
Paul Sintenis in 1886.
There is new information suggesting
the existence of one population within
the Tortuguero Lagoon in northern
Puerto Rico (Beverly Yoshioka, Service,
pers. comm., 2013). This will be the first
record for the species in the northern
coast of Puerto Rico. The finding of this
new locality is supported by the
existence of the species on a similar
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Jkt 232001
habitat in the Island of Anegada (British
Virgin Islands). Varronia rupicola is
also found in the northwest section of
Anegada, where it is reported as
common (Clubbe et al., 2004, p. 344;
McGowan et al., 2006, p. 5).
other natural or manmade factors
affecting its continued existence. Listing
actions may be warranted based on any
of the above threat factors, singly or in
combination. Each of these factors is
discussed below.
Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1533),
and its implementing regulations at 50
CFR part 424, set forth the procedures
for adding species to the Federal Lists
of Endangered and Threatened Wildlife
and Plants. Under section 4(a)(1) of the
Act, we may list a species based on any
of the following five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; and (E)
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
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Agave eggersiana
The Agave eggersiana population
found in Great Pond is the only one
located in a conservation area. The
remaining populations occur within
privately owned lands and are
threatened by development, or are
growing in areas that are already
developed and managed as tourism and
residential projects and that will not
support the continued existence of the
plants. Based on information reported
by the University of the Virgin Islands’
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Conservation Data Center (USVI–
CLWUP 2004), at least three of the
populations (i.e., Protestant Cay,
Gallows Bay, and Manchenil Bay) lie
within areas identified by DPNR as
high-density land use areas, and thus
have a higher susceptibility to
development in the near future. The
coastal areas that harbor suitable habitat
for the species are currently subject to
urban and tourist development (O.
Monsegur and M. Vargas, Service, pers.
obs., 2010 and 2013). At least two
proposed development projects have
been identified within suitable habitat
for the species (i.e., C&R Robin, LLC,
and Seven Hills Beach Resort and
Casino) (Weiss, CBD, pers. comm.,
2010). Current information regarding the
status of these development projects is
not available to the Service.
The population at Protestant Cay has
been affected by construction and
management activities associated with
the current use of the area, i.e., the
disposal of garden debris from a hotel in
the species’ known habitat (O.
Monsegur and M. Vargas, Service, pers.
obs., 2010). As Agave eggersiana relies
on asexual reproduction, the species
depends on the bulbils becoming
established. Covering the bulbils with
debris may result in subsequent
mortality of the bulbils and lack of
natural recruitment, thus affecting the
long-term survival of this population.
Moreover, individuals located on the
edges of the population are pruned as
part of the gardens’ maintenance. This
practice may result in mortality or
mutilation of individuals because the
species is monopodial (single growth
axis). The population at Protestant Cay
is also threatened by competition with
nonnative plant species. In this case,
habitat modifications from urban
development (e.g., road) and garden
maintenance have created conditions for
the establishment of invasive, nonnative
species. Also, the undeveloped habitat
on the cay is being rapidly colonized by
nonnative species (see Factor E
discussion, below). A. eggersiana plants
also seem to be stressed by competition
with nonnative plants.
Another modification of habitat in the
area was a sand ramp constructed in
2011, on the northeast side of the cay (T.
Cummins and W. Coles, DPNR, pers
comm., 2011; R. Platenberg and T.
Cummins, DPNR, pers. comm., 2012;
Zegarra, Service, pers. comm., 2012). It
was documented that at least five
individuals of Agave eggersiana were
crushed or otherwise impacted by the
excavation work (R. Platenberg and T.
Cummins, DPNR, pers. comm., 2012).
The individuals located at Gallows
Bay are within a developed residential
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complex that has the potential for future
expansion, and thus may affect Agave
eggersiana (O. Monsegur and M. Vargas,
Service, pers. obs., 2010 and 2013).
Moreover, the Gallows Bay area does
not contain additional habitat to allow
for population expansion. Remaining
forested areas surrounding this location
are characterized by an abundance of
nonnative species. The small pockets
that could be colonized by bulbils are
occupied by Sansevieria cylindrica
(African spear), a nonnative plant
species that tends to form a complete
cover of the understory (see Factor E
discussion, below).
The area from Cane Garden Bay to
Manchenil Bay on the south coast of St.
Croix harbors four of the known natural
populations of Agave eggersiana
(Manchenil Bay, Vagthus Point, Cane
Garden, and South Shore). According to
DPNR personnel (Valiulis, pers. comm.,
2010), these areas are advertised by
realtors for tourism and residential
development. Furthermore, the areas
along the south coast that have not been
developed are used for cattle or hay
production, minimizing the recovery of
native vegetation and, therefore, the
habitat for A. eggersiana (O. Monsegur
and M. Vargas, Service, pers. obs., 2010
and 2013). The development of tourist
and residential projects in these coastal
areas may result in the extirpation of
some populations or, at the least, will
reduce the chances of the populations to
expand or to colonize other areas. The
effects of development projects are
exacerbated by the low potential for
natural recruitment due to the small
number of populations and individuals.
The population of Great Pond is
located between the entrance road of the
East End Marine Park office and a
private property currently advertised for
sale. The population seems to be
healthy based on the presence of
different size plants and evidence of
recent flowering events. However, the
area near the population is mowed, and
the access road limits the expansion of
the population. Furthermore, the
property adjacent to the population is
privately owned and currently for sale
(O. Monsegur and M. Vargas, Service,
pers. obs., 2010 and 2013). The possible
use of the area for additional residential
or tourist development may affect the
Agave eggersiana population. Owners
will likely manage their properties as
landscapes, which could lead to land
clearing, additional mowing, other
maintenance activities, and the
introduction of nonnative plants.
Moreover, the abundance of grasslands
and the dominance of the nonnative
plant Megathyrsus maximus (guinea
grass) make the population of A.
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eggersiana susceptible to humaninduced fires (addressed under Factor E,
below).
Gonocalyx concolor
Habitat destruction and modification
have been identified by species expert
as the main threat to Gonocalyx
concolor (Proctor 1992, p. 3; O.
Monsegur, UPRM, unpubl. data, 2006;
C. Pacheco and O. Monsegur, Service,
unpubl. report, 2013, p. 3). In 1974, the
Commonwealth of Puerto Rico granted
special use permits for the construction
of telecommunications facilities, and
governmental and recreational facilities,
within G. concolor habitat, affecting
approximately 107 ac (43.5 ha) of lower
montane very wet forest (Silander et al.
1986, p. 178). Currently known
populations of G. concolor at Cerro La
Santa are found in remnants of elfin
forest vegetation located adjacent (less
than 246 ft (75 m)) from
telecommunication facilities, and at the
edges (less than 9.8 ft (3 m)) of the road
that provide access to the
telecommunication facilities (C.
Pacheco and O. Monsegur, Service,
unpubl. report, 2013, p. 3). Below we
discuss the three factors that may affect
the current habitat or range of G.
concolor: (1) Installation of
telecommunication towers; (2) road
improvement; and (3) vegetation
management.
Land-use history of Cerro La Santa
has shown that installation of
telecommunication facilities for
television, radio, and cellular
communication, and for military and
governmental purposes, has adversely
impacted Gonocalyx concolor habitat
(Silander et al., 1986, p. 178), and
although not documented, presumably
has directly affected individuals of the
species. George Proctor (1992, p. 3)
stated that the construction of a paved
road and gigantic telecommunication
towers on the summit ridge of Cerro La
Santa destroyed much of the natural
population of this species. Currently,
the telecommunication tower and its
associated facilities (i.e., access roads,
security fences, guy wires) occupy
approximately 6.1 ac (2.5 ha) of the elfin
forest in Cerro La Santa; this is habitat
that the species may have occupied in
the past (C. Pacheco and O. Monsegur,
Service, unpubl. report, 2013, p. 3).
Although the populations at Cerro La
Santa are located within a
Commonwealth forest, this area is
subjected to development for expansion
of telecommunication infrastructure
because permits to build new
communication facilities or expand
currently existing ones within or near
Commonwealth forests are prevalent
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(DNER 2004a, p. 2). Expansion of the
existing telecommunication facilities
may result in loss of 27 individuals of
G. concolor and their habitat. In Puerto
Rico, towers for cellular
communication, radio, television, and
military and governmental purposes
have represented a threat to those plant
species that happen to occur only on
mountaintops. The proliferation of these
antennas has increased with the advent
of cellular phone and related
technologies. While the towers
themselves may not occupy a very large
area, construction activities, access
roads, and other facilities have a much
wider impact, resulting in the
elimination of potential habitat for the
species.
For the above reasons, we determined
that installation of additional
communications towers or expansion of
the existing one at Cerro La Santa is a
threat to Gonocalyx concolor by direct
mortality and due to permanent loss,
fragmentation, or alteration of its
habitat.
Construction of a new access road and
improvement of the existing access road
to the existing communication facilities
have been identified as a factor that
could directly (destruction of
individuals) or indirectly (slope
instability and habitat degradation)
reduce the number Gonocalyx concolor
and its habitat at Cerro La Santa (Proctor
1992, p. 3; C. Pacheco and O. Monsegur,
Service, unpubl. report, 2013, p. 3).
Further, expanding the road that
provides access to the
telecommunication facilities may
negatively affect the species’ habitat and
could result in loss of 11 mature
individuals of G. concolor (C. Pacheco
and O. Monsegur, Service, unpubl.
report, 2013, p. 3). Additionally,
clearing the native vegetation along the
road may facilitate and accelerate
colonization of invasive vegetation
towards G. concolor habitat (see Factor
E discussion, below). Destruction or
modification of this kind of habitat may
be irreversible. Therefore, the
microhabitat conditions necessary for
the recovery of the species may be lost
if the habitat is modified for the
expansion of the existing
telecommunications facilities or
construction of new communication
facilities.
Vegetation management around the
existing telecommunication towers and
associated facilities and along the
existing power lines that energize these
facilities is a threat to Gonocalyx
concolor and its habitat (C. Pacheco and
O. Monsegur, Service, unpubl. report,
2013, p. 3). Telecommunication
companies periodically remove
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vegetation along the access roads,
around the security fences, and under
the guy wires (tensors) that are anchored
in the forest. Additionally, maintenance
staff of the Puerto Rico Energy and
Power Authority (PREPA) periodically
trim and clear the vegetation under the
existing power lines that provide energy
to the telecommunication facilities and
adjacent communities. Presently, the
Puerto Rico Department of Natural and
Environmental Resources (DNER) is
aware of the presence of G. concolor and
the need to implement conservation
measures for the species in Cerro La
Santa. The existing telecommunication
facilities and PREPA usually have a
restricted perimeter delimiting the area
that can be mowed and trimmed.
However, maintenance activities outside
of the perimeter have been conducted
without the coordination with the forest
manager, affecting the forest vegetation
and G. concolor habitat (Hecsor SerranoDelgado, DNER, pers. comm., 2013; O.
Monsegur, UPRM, unpubl. report, 2006,
p.1). In 2006, Omar Monsegur
documented damages to an individual
of G. concolor caused by vegetation
removal activities outside of the fences
(O. Monsegur, UPRM, unpubl. report,
2006, p.1). Additionally, clearing the
native vegetation along the access roads,
around the telecommunication facilities,
and under the power lines may facilitate
and accelerate colonization of invasive
vegetation in G. concolor habitat. See
Factor E, below, for further discussion
on invasive species.
Even though the population dynamics
of the species are poorly known, we
understand that the impacts discussed
above could be detrimental to the
species as a whole. Clearing of
vegetation may result in direct impacts
(cutting of individuals) or indirect
impacts (by opening forest gaps that can
serve as corridors for invasive species)
to the species. Vegetation management
and maintenance of communication
towers and facilities are a threat to
Gonocalyx concolor due to changes in
microclimate (a local atmospheric zone
where the climate differs from the
surrounding area) and plant species
composition. Also, vegetation
management around the existing
facilities and along the access roads may
be a direct and indirect threat to the G.
concolor because it may alter the habitat
condition, allowing invasive plants to
colonize the area, and may result in
direct physical damage to the species.
Varronia rupicola
The species’ rarity and restricted
distribution make it vulnerable to
habitat destruction and modification.
About 50 percent of known Varronia
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rupicola individuals in Puerto Rico
occur on private lands (i.e., Yauco,
˜
Penuelas, and Ponce) in areas subject to
urban development. Moreover, the
˜
habitat at Penuelas and Ponce may
remain underestimated in relation to the
presence of the species as the area has
not been extensively explored. The
˜
habitat in the municipalities of Penuelas
and Ponce has been severely fragmented
for urban development (i.e., housing
projects, hotels, jails, landfills, rock
quarries, and Puerto Rico Highway
Number 2 (PR 2)). The habitat has been
further fragmented by the use of these
forested areas by PREPA as a right-ofway for power lines, and additional
habitat was impacted for a former
proposed gas pipeline (Gasoducto Sur).
At least 1,200 ac (485 ha) of prime dry
´
forest habitat from Guanica to Ponce are
currently proposed for urban and
industrial developments, which are
evaluated by the Puerto Rico planning
board (https://www.jp.gobierno.pr).
These include the areas where the
Ponce populations were recently located
by Service staff. Future projects may
threaten these populations with
fragmentation, and possibly extirpate
currently known individuals. Despite
the species’ biology suggesting its ability
to colonize disturbed areas, it is very
likely that once the habitat is
fragmented. V. rupicola will be
outcompeted by nonnative plant species
(see Factor E discussion).
˜
In Penuelas, the species is found in an
area that is currently under urban
development. Breckon and Kolterman
(1996) reported a healthy population of
Varronia rupicola in this area located at
˜´
El Penon de Ponce (Municipality of
˜
Penuelas), which is part of a residential
´
development called ‘‘Urbanizacion El
˜´
Penon.’’ At this site, V. rupicola plants
grows within residential lots, and
although the lots are large in size,
current and ongoing construction and
deforestation (some lots have been
completely cleared for house
construction) threaten this population.
In 2007, Monsegur and Breckon (2007,
p. 6) reported that one individual plant
´
˜
adjacent to ‘‘Urbanizacion El Penon’’
was eliminated by the improvement of
PR 2. The authors reported that
vegetation was removed and the area
was bulldozed, apparently as part of a
project to control run-off from the
ravine.
In Yauco, the species occurs within
private properties that may be subject to
urban development (https://
www.jp.gobierno.pr). In fact, urban
development has encroached remnants
of native dry forest areas, resulting in
the isolation or disjunction of
populations of rare plants, hence,
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reducing suitable habitat for the species.
These areas are also threatened by
deforestation for agricultural practices
such as raising cattle, cattle grazing, and
for the extraction of fence posts (O.
Monsegur, Service, pers. obs., 2005).
The known population at Yauco was
observed at the edge of an existing dirt
road. Therefore, any road expansion
may result in the extirpation of
individuals, habitat modification, and
intrusion of nonnative plants.
´
In the Guanica Commonwealth Forest
and the Vieques Island National
Wildlife Refuge (NWR), Varronia
rupicola is found at the edge of trails
and roads, making the species prone to
be affected by management activities
(e.g., widening of trails, road repairs).
Additionally, several individuals of V.
rupicola are found underneath power
´
lines of PREPA at the Guanica
Commonwealth Forest, where they are
threatened by maintenance activities
such as cutting or the use of herbicides.
PREPA has the right to access the power
lines for maintenance and service in
case of emergencies. Damage to
individual plants caused by
maintenance activities has been
observed in the past (O. Monsegur,
Service, pers. obs., 2009). This makes a
´
significant part of the Guanica
populations prone to extirpation despite
the existence of regulatory mechanisms
(see Factor D discussion, below).
Furthermore, despite being a National
Wildlife Refuge, the Vieques site (Puerto
Ferro) is considered as an active
ammunition site due to the previous use
of Vieques Island as a bombing range by
the U.S. Navy (https://public.lantopsir.org/sites/public/vieques/
default.aspx). Although there are no
current plans to conduct vegetation
removal to investigate the ammunitions
in Puerto Ferro (F. Lopez, Service, pers.
comm., 2013), the investigation process
at Vieques has proved to be dynamic
and there is a possibility that clearing of
native vegetation will be required to
conduct removal of ammunitions in the
future.
Varronia rupicola is also found in the
western half of Anegada Island, and the
population appears to be healthy.
However, despite efforts to maintain
biodiversity and promote conservation
on Anegada, V. rupicola, along with
other rare plant species and their
preferred limestone habitat, faces threats
of future habitat fragmentation, habitat
modification, and invasive species
(Pollard and Clubbe 2003, p. 5;
McGowan et al., 2006, p. 4). Anegada is
under heavy pressure for residential and
tourism development (McGowan et al.,
2006, p. 4), resulting in improvement
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and construction of roads, which
increase habitat loss and fragmentation.
About half of known populations and
suitable habitat are within privately
owned land, which is being modified or
proposed to be modified for urban
development. These activities are
expected to continue.
Conservation Efforts To Reduce the
Present or Threatened Destruction,
Modification, or Curtailment of Its
Habitat or Range
Agave eggersiana
Efforts to re-establish locally
endangered plant species to the wild are
occurring within properties managed by
the National Park Service (NPS) (SARI
and Buck Island Reef National
Monument) on St. Croix. The intent of
NPS is to increase production of the
species’ progeny around the island,
which started in 2007, by planting seven
individuals of Agave eggersiana (NPS,
unpubl. data, 2007). Also, an intraagency agreement between the Service
and NPS, in cooperation with the
Florida and Caribbean Exotic Plant
Management Team, was established in
2007, to control nonnative, invasive
plants and restore coastal landscape.
The agreement was to restore
approximately 15 acres (6.1 ha) of SARI
coastal wetlands and uplands. The
agreement also included planting A.
eggersiana among other native flora.
Currently, there are more than 100
juvenile plants on NPS lands. However,
there is the need to continue monitoring
these plants to document their longterm survival and recruitment, and to
adaptively manage the population.
Other efforts include the evaluation of
the status of the natural populations by
Service staff. In 2010 and 2013, Service
biologists visited St. Croix and found
Agave eggersiana planted at the Lagoon
Picnic Area, a public beach that seems
to be under a reforestation effort funded
by the Antilitter and Beautification
Commission. The site harbors about 220
plants that are part of the landscape.
Although the Service has no
information on the reforestation project,
it seems to be a good effort for the
protection of coastal habitat and as an
outreach effort towards the protection of
the species.
Gonocalyx concolor
Gonocalyx concolor populations
occur on public lands managed for
conservation by the Puerto Rico DNER.
The DNER develop a management plan
for all Commonwealth Forests in 1976;
however, specific measures to protect
this species are not included in the plan
(DNR 1976, pp. 168–181). Currently,
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activities to be conducted within
Commonwealth Forest are generally
scrutinized, and measures to minimize
or avoid impacts to species protected by
DNER and Federal agencies are
recommended and implemented (see
Factor D discussion). However,
authorized activities, such as vegetation
clearing around communication towers,
under power lines, and along roads,have
been documented, resulting in loss of
individuals and the species’ habitat.
Varronia rupicola
The Service’s Caribbean Ecological
Service Field Office (CESFO) has
evaluated federally funded projects or
federally related projects requiring
federal permits that lie within the
species’ range. As part of the evaluation,
the Service recommends surveys to
identify populations and recommends
conservation measures to protect the
species. However, residential projects
without Federal nexuses are not
submitted to the Service for evaluation.
Summary of Factor A
Agave eggersiana
The threats of possible construction
and developments, and the current
management of the habitat of the
populations, may further limit the
species. Direct consequences can be
expected as impacting (harming) the
individuals (e.g., cutting or mowing),
while indirect consequences can be
expected to create a habitat disturbance
where nonnative plants can overpower
Agave eggersiana. Currently, there
continue to be impacts on various
populations that are expected to
continue into the future.
Gonocalyx concolor
The species’ rarity and restricted
distribution makes it vulnerable to
habitat destruction and modification.
The scope of these factors is exacerbated
because the most significant portion of
the known population occurs adjacent
to telecommunication facilities and at
the edge of the existing access road. The
activities related to these facilities are
expected to continue into the future.
Therefore, they are likely to have
significant impact on Gonocalyx
concolor.
Varronia rupicola
Degradation of habitat represents a
threat to Varronia rupicola. About half
of the known populations of V. rupicola
and its suitable habitat are within
privately owned land, which is being
modified or is proposed to be modified
for urban development. In addition,
habitat fragmentation by clearing of
vegetation, road constructions, and
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right-of-way maintenance (cutting
plants and used of herbicides) can limit
the species’ survivability where these
activities create the conditions for
nonnative plants to outcompete V.
rupicola. We expect that this threat
would continue into the future.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
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Agave eggersiana
Agave eggersiana has been reported as
a cultivar since it was described as a
species in 1913 (Trelease 1913, p. 28).
Historically, the majority of A.
eggersiana found on St. Croix and St.
Thomas were from landscaped areas
(Britton and Wilson 1923, p. 156;
Plaskett, DPNR, pers. comm., 2003;
Kojis and Boulon, DPNR, pers. comm.,
´
1996; Proctor and Acevedo-Rodrıguez
´
2005, p. 118; Acevedo-Rodrıguez, pers.
comm., 2005). Currently, the species is
distributed by the St. George Botanical
Garden and the St. Croix Environmental
Association for conservation and private
landscaping purposes. In fact, it is an
ornamental species commonly used on
the island of St. Croix. Recent declines
in the number of individuals at one
population along the coast of Manchenil
Bay are thought to be due to collection
for ornamental purposes (DalmidaSmith, DPNR, pers. comm., 2010;
Valiulis, DPNR, pers. comm., 2010). At
present, we do not have evidence to
confirm this threat. However, when
Service biologists visited the island in
2010 and 2013, they observed that A.
eggersiana continues to be used as a
landscape species.
Current evidence suggests that the
wild and cultivated populations of
Agave eggersiana have minimum
genetic variation. Data suggest that
cultivated individuals could be used as
genetic stock to aid in the long-term
survival of this species. However, most
cultivated populations are groomed and
do not allow natural recruitment.
Therefore, we are concerned about
possible collection of individuals from
natural populations for landscaping.
The rarity and low numbers of
individuals for this agave may result in
a high ornamental value. The limited
reproduction of the plant, which
reproduces only once every 10 to 15
years (D. Hamada, SGVBG, pers. comm.,
2010), may lead people to collect
individuals from the wild and thus
lower the recruitment of those limited
populations and risk the continued
survival of the species.
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Gonocalyx concolor
Gonocalyx concolor is not a
commercially valuable species or a
species sought after for recreational or
educational purposes. However, the
species is recognized by its rarity and
restricted range, making it more
attractive to collectors and scientists.
Collection could be a significant threat
to the species due to the few remaining
populations, small population size,
restricted range, remoteness of occupied
habitat, and the potential for collection
to occur at any time. Because little is
known about G. concolor (i.e.,
abundance, distribution, habitat
requirement, and phenology), any
collection of seedlings, saplings,
flowers, fruits, or parts of the individual
without appropriated evaluation of its
effect on the species could adversely
affect the status of the population. Even
limited collection from the remaining
population could have deleterious
effects on reproductive and genetic
viability of the species and could
´
contribute to its extinction (Jose
Sustache, DNER, pers. comm., 2013).
Although we consider collection to be a
potential threat to this species, we do
not have information indicating that the
species is being collected for
commercial, recreational, scientific or
educational purposes.
Varronia rupicola
There is scientific interest in Varronia
rupicola from local and external
botanists. In fact, there is ongoing
research by personnel from the Royal
Botanic Gardens (KEW) related to the
reproductive biology, propagation, and
genetics of this species, including the
populations from United States and
British territories (entire Puerto Rican
platform). However, the current
available information on the species
does not suggest that overutilization for
commercial, recreational, scientific, or
educational purposes has contributed to
a decline of V. rupicola. This research
is the only known use of the species,
and it is strictly for scientific purposes.
Therefore, despite its rarity, we do not
have any evidence that suggests this
threat is negatively impacting V.
rupicola.
Conservation Efforts To Reduce
Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Agave eggersiana
At present, the Service is unaware of
any conservation efforts to reduce
overutilization for commercial,
recreational, scientific, or educational
purposes of Agave eggersiana, except
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for the existing regulatory mechanisms
that protect the species. However,
although A. eggersiana is protected by
Act No. 5665, the USVI law that
provides protection to indigenous,
endangered, and threatened fish,
wildlife, and plants in the Territory, the
use of the species for landscaping
continues to be a practice. This law
prohibits the collection of endangered
species. However, we do not have
information about enforcement
mechanisms to avoid the use of this
plant for landscaping (see Factor D
discussion, below).
Gonocalyx concolor and Varronia
rupicola
´
The Carite and Guanica
Commonwealth Forests are managed for
conservation by the Puerto Rico DNER,
and collection of any plant in these
lands is regulated by Commonwealth
Law No. 133. Currently, there are
permits to collect plants in the Carite
´
and Guanica Commonwealth Forests.
However, such permits are issued by
DNER after determining that proposed
actions will not negatively affect the
´
species (Jose Sustache, DNER, pers.
comm., 2013; see Factor D discussion,
below). If this proposed rule is adopted,
collection of Varronia rupicola at the
Vieques National Wildlife Refuge will
require a special use permit and section
7 consultation (see Factor D discussion,
below).
Summary of Factor B
Agave eggersiana is recognized as an
ornamental plant, and is locally
distributed by botanical gardens (St.
George Village Botanical Garden) and
the St. Croix Environmental Association
to residents for use in private gardens.
Therefore, we consider collection to be
a threat to the species due to the few
remaining natural populations.
Overcollection from natural populations
may compromise the natural
recruitment and the recovery of Agave
eggersiana. We do not believe that
overcollection is a threat to Gonocalyx
concolor or Varronia rupicola.
Factor C. Disease or Predation
Agave eggersiana
The genus Agave is widely affected by
the agave snout weevil (Scyphophorus
acupunctatus). This weevil has a wide
distribution that includes the Greater
Antilles (i.e., Cuba, Jamaica, Hispaniola,
and Puerto Rico) (Vaurie 1971, p. 4;
Setliff and Anderson 2011, p. 1). The
larvae of this weevil feed on the starchy
base of the plant, increasing the risk of
infestation by pathogens such as a virus
or fungus, later resulting in the death of
the plant (Vaurie 1971, p. 4). At this
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time, there is no information about the
occurrence of the agave snout weevil
within St. Croix. However, it has been
documented to be found on adjacent
islands such as St. Thomas and Water
Island (USVI—https://www.uvi.edu/
community/cooperative-extensionservice/agriculture-and-naturalresources/integrated-pestmanagement.aspx).
Although we do not have evidence on
the agave snout weevil’s presence on St.
Croix, due to the low number of natural
populations of Agave eggersiana and the
abundance of vectors (i.e., nonnative
agaves planted in gardens), we consider
that the weevil’s arrival to this island is
forthcoming. The agave snout weevil’s
presence on nearby islands is a concern
especially where there is constant traffic
(commuting) among islands with local
and international trade. This could
potentially increase the risk of this
weevil to arrive and infest the island at
any time. Moreover, the island of St.
Croix harbors other types of Agave,
which could potentially become
stepping stones for the weevil to spread
around and affect the few and limited
populations of A. eggersiana.
Service biologists documented that a
small number of individuals of Agave
eggersiana were observed with scarring
along the borders of some leaves (O.
Monsegur and M. Vargas, Service, pers.
obs., 2010). It appears that an insect or
arthropod larva may feed on these
leaves. However, the exact cause and
the consequences of the scarring remain
unknown. Nevertheless, this is
important and should be monitored, as
it might be an indicator of a recently
arrived pest to St. Croix.
On Mona Island, Puerto Rico, feral
pigs are known to uproot juveniles and
destroy the root system of Agave
sisalana (sisal) to feed on the root
system or to use them as a water source
(J. Saliva, Service, pers. obs, 1983 and
1996.). As introduced pigs, donkeys,
and goats have been reported on St.
Croix, we cannot disregard the possible
predation of Agave eggersiana,
particularly young plants, by these feral
animals. The absence of evidence of
predation by these species might be the
result of the low number of individuals
of A. eggersiana, their isolation, and the
proximity of some of these populations
to human-inhabited areas. Nonetheless,
at this time there is no evidence that
donkeys, pigs, or goats constitute a
direct threat to A. eggersiana.
Gonocalyx concolor and Varronia
rupicola
No insect pest or predation of
individuals of Gonocalyx concolor or
Varronia rupicola has been documented
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in the wild. Minor to moderate
infestation by glasshouse whitefly
(Trialeurodes vaporariorum) was
observed on cultivated material of V.
rupicola at the Royal Botanical Garden,
KEW (Wenger et al. 2010). However,
this was suspected to be the result of the
proximity of the V. rupicola material to
a species that is highly susceptible to
this insect pest.
Due to the low number of individuals
and populations of these species,
disease and predation could certainly be
threats. However, we have no further
information indicating that disease or
predation are a current threat to
Gonocalyx concolor or Varronia
rupicola. We do not consider disease or
predation to be a threat to either of the
two species.
Conservation Efforts To Reduce Disease
or Predation
Agave eggersiana, Gonocalyx concolor,
and Varronia rupicola
Based on the information available,
we have no evidence of conservation
efforts to prevent or reduce adverse
effects due to disease or predation. So
far, the only species that could be
potentially affected by an insect pest is
Agave eggersiana. However, to our
knowledge, no conservation measure
has been implemented in this regard.
Summary of Factor C
Predation (scaring) has been observed
in some individuals of Agave
eggersiana, but there is no direct
evidence that the severity of this
stressor has affected the species.
However, disease caused by the agave
snout weevil could potentially affect A.
eggersiana at a population level. Thus,
based on our analysis of the best
available scientific and commercial
available data, we find that disease may
be a significant stressor to the overall
status of A. eggersiana by affecting the
long-term survival of the species.
We have no information indicating
that disease or predation is a current
threat to Gonocalyx concolor or
Varronia rupicola.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Under this factor, we examine
whether existing regulatory mechanisms
are inadequate to address the threats to
Agave eggersiana, Gonocalyx concolor,
and Varronia rupicola discussed under
other factors. 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
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under the Act, we interpret this
language to require the Service to
consider relevant Federal, State, and
Tribal laws and 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
Agave eggersiana, Gonocalyx concolor,
and Varronia rupicola.
Agave eggersiana
Territory
The Territory of the U.S. Virgin
Islands currently considers Agave
eggersiana as endangered under the
Virgin Islands Indigenous and
Endangered Species Act (Law No. 5665)
(V.I. Code, Title 12, Chapter 2). This
law, signed in 1990, amended an
existing regulation (Bill No. 18–0403) to
provide for the protection of endangered
and threatened wildlife and plants by
prohibiting the take, injury, or
possession of indigenous plants. As we
mentioned above, A. eggersiana is
currently being used for private
landscaping on St. Croix. At present, we
do not have information about the
sources of the individuals used for such
purposes. However, we are concerned
about the removal of individuals from
natural populations for landscaping.
Based on the number of individuals
currently used for private gardens and
the landscape practices in private areas,
such as pruning and mowing of
populations, we believe that protection
provisions under local regulation may
not be appropriately enforced.
Rothenberger et al. (2008, p. 68)
indicated that the lack of management
and enforcement capacity continues to
be a significant challenge for the USVI,
because enforcement agencies are
chronically understaffed and territorial
resource management offices experience
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significant staff turnover, particularly
during administration changes.
Based on the above, although there is
a regulatory mechanism that protects
Agave eggersiana on St. Croix, we
consider that the enforcement of the
mechanism is inadequate.
Gonocalyx concolor and Varronia
rupicola
Federal
One of the currently known
populations of Varronia rupicola lies
within the Vieques NWR (Puerto Ferro
population). Collecting and managing
plant material (including seeds) within
a national wildlife refuge are regulated
and require a permit from the refuge
manager (FWS Form 3–1383–R). The
National Wildlife Refuge System
Administration Act of 1966 (16 U.S.C.
668dd–668ee, as amended by the
National Wildlife Refuge System
Improvement Act of 1997) provides
guidance for management and public
use of the refuge system.
tkelley on DSK3SPTVN1PROD with PROPOSALS
Commonwealth
In 1999, the Commonwealth of Puerto
Rico approved the Law No. 241, also
known as New Wildlife Law of Puerto
Rico (‘‘Nueva Ley de Vida Silvestre de
Puerto Rico’’). The purpose of this law
is to protect, conserve, and enhance
both native and migratory wildlife
species, including plants; declare all
wildlife species within its jurisdiction
as property of Puerto Rico; and regulate
permits, hunting activities, and
nonnative species, among others.
However, as we mentioned above under
the Factor A discussion, some
individuals of Gonocalyx concolor and
Varronia rupicola have been pruned,
and in some cases eliminated, as result
of unauthorized activities such as
vegetation removal within the
Commonwealth Forest (O. Monsegur,
UPRM, unpubl. report, 2006, p. 1) and
within privately owned lands
(Monsegur and Breckon 2007, p. 6).
Therefore, we believe that protection
provisions under the Law No. 241 are
not being appropriately enforced.
In 1998, the Commonwealth of Puerto
Rico approved the Commonwealth Law
No. 150, known as Puerto Rico Natural
Heritage Law (Ley del Programa de
Patrimonio Natural de Puerto Rico). The
purpose of the Law No. 150 is to create
the DNER Natural Heritage Program.
This program has the responsibility to
identify and designate as critical
elements some rare, threatened, or
endangered species that should be
considered for conservation, because of
their contribution to biodiversity and
because of their importance to the
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natural heritage (DNR 1988, p.1).
Currently, Gonocalyx concolor and
Varronia rupicola are considered as
critical elements by the DNER Natural
Heritage Program. The Law No. 150
does not provide penalties for actions
that may adversely affect critical
elements; however, the law triggers
other Commonwealth laws and
regulations, such as Law No. 133 and
Regulation No. 6769 (see below), that
provide protection to critical elements.
´
The Carite and Guanica
Commonwealth Forests are protected by
Law No. 133 (12 L.P.R.A. sec. 191),
1975, as amended, known as the Puerto
Rico Forest Law (‘‘Ley de Bosques de
Puerto Rico’’), as amended in 2000.
Section 8(A) of Law No. 133 prohibits
cutting, killing, destroying, uprooting,
extracting, or in any way damaging any
tree or vegetation within a
Commonwealth forest without
authorization of the Secretary of the
DNER. Although management plans for
Commonwealth forests include the
protection and conservation of species
classified under DNER regulations as
critical element, endangered, or
threatened, on occasions the location of
such species in the forests makes
enforcement of these regulations a
difficult task. As previously mentioned,
Gonocalyx concolor and Varronia
rupicola are located adjacent to trails,
near access roads, and below power
lines, where they are susceptible to
maintenance practices. According to
DNER forest managers, on several
occasions, coordination between forest
personnel and field staff from PREPA
has not been effective to avoid damaging
species protected by Commonwealth
laws, including V. rupicola and G.
concolor (M. Canals, DNER, pers. comm.
2008; H. Serrano-Delgado, DNER, pers.
comm. 2013).
In 2004, the Commonwealth of Puerto
Rico adopted Regulation No. 6769,
Regulation of Special Permits for the
Use of Communications and Buildings
Associated to Electronic Systems of
Communication within Commonwealth
Forests in Puerto Rico (‘‘Reglamento de
Permisos Especiales para Uso de
Comunicaciones y Edificaciones
´
Asosiadas a Sistemas Electronicos de
´
comunicacion en los Bosques
Estatales’’), which provides guidance for
the installation and maintenance of
telecommunication facilities within
Commonwealth forests and for the
protection of natural resources. Article
7(d) of this regulation states that during
installation, operation, and maintenance
of telecommunication facilities,
conservation measures should be taken
to avoid or minimize impacts on species
protected by DNER and Federal agencies
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(DNER 2004a, p. 13). However,
individuals of Gonocalyx concolor have
been affected by maintenance activities
of existing communication facilities,
making implementation of this
regulation a challenging task (see
discussion under Factor A, above, and
Factor E, below).
In 2004, DNER approved Regulation
6766 to regulate the management of
threatened and endangered species in
the Commonwealth of Puerto Rico
(‘‘Reglamento para Regir el Manejo de
las Especies Vulnerables y en Peligro de
´
Extincion en el Estado Libre Asociado
de Puerto Rico’’). Article 2.06 of
Regulation 6766 prohibits collecting,
cutting, and removing, among other
activities, listed plants within the
jurisdiction of Puerto Rico. Gonocalyx
concolor and Varronia rupicola are not
included in the list of protected species
under Regulation 6766. However, as
indicated above, Law No. 241 provides
protection to all wildlife species
(including plants) under
Commonwealth jurisdiction, even those
on private lands.
Local Ordinances
On the island of Anegada, there are
various conservation and education
efforts taking place for the protection of
rare plant and animal species (Wenger
et al. 2010, p. 8). However, we are
unaware of any formal regulatory
mechanism for protecting Varronia
rupicola. On November 3, 1999, a
portion of western Anegada (2,646 ac
(1,071 ha)) was designated as a Ramsar
site and added to the List of Wetlands
of International Importance (Western
Salt Ponds of Anegada). A portion of the
preferred limestone habitat of V.
rupicola lies within this site, which is
owned by the British government.
Although this designation does not
necessarily provide legal protection
status, the purpose of Ramsar sites is to
ensure the perpetuation of ecological
functions of those sites by means of a
wise-use approach.
Summary of Factor D
Agave eggersiana, Gonocalyx
concolor, and Varronia rupicola and
their habitats are partially protected by
Federal, Commonwealth, Territory, and
local regulations. However, after
evaluating the information available on
the implementation of the existing laws,
we determined those regulatory
mechanisms do not provide adequate
protection to the species. The
enforcement of existing laws has not
been effective, because harming or
injuring (mowing or pruning) Agave
eggersiana has been reported. In
addition, the implementation and
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enforcement of effective measures to
protect individuals of V. rupicola
located adjacent to existing trails and
below power lines within
Commonwealth forests have not been
effective. The same problem has
occurred with G. concolor during
maintenance of communication towers.
Additionally, it is important to note that
enforcement on private lands continues
to be a challenge, as accidental damage
or extirpation of individuals has
occurred due to lack of knowledge of
the species by private landowners.
Factor E. Other Natural or Manmade
Factors Affecting Their Continued
Existence
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Invasive Species
Invasive plant species can affect
native ecosystems at three levels: the
genetic level, where the number of
individuals of native species can be
reduced below the minimum necessary
for persistence; the species diversity
level, where the number of species
present and their distribution can be
reduced; and the ecosystem level, where
the functioning of the ecosystem can be
changed (Rippey et al. 2002, p. 170).
Nonnative species can be very
aggressive and compete with native
species for sunlight, nutrients, water,
and ground cover. Once established,
these nonnative species typically
dominate the landscape, and the novel
forest is characterized by a decrease in
the number of endemics (Lugo and
Helmer 2003, p. 145). The impacts of
invasive species are among the greatest
threat to the persistence of native rare
species and their habitats (Thomson
2005, p. 615).
Varronia rupicola and Agave eggersiana
Although invasive plant species have
not been documented as a current threat
to Varronia rupicola, they may become
so in the future. Studies conducted
´
within the Guanica Commonwealth
Forest indicate that some nonnative tree
species (e.g., Leucaena leucocephala)
can persist as a dominant canopy
species for at least 80 years (Wolfe 2009,
p. 2). The same is expected to occur
with nonnative grass species (e.g.,
Megathyrsus maximus). These invasive
species may invade recently disturbed
(naturally or by human impacts) areas
and occupy the suitable habitat of V.
rupicola. Despite the quality and overall
diversity of the habitat that harbors V.
rupicola populations in the southern
coast of Puerto Rico, recent
developments and habitat fragmentation
have served as corridor for invasive
species (e.g., right-of-way for the former
Gasoducto Sur; O. Monsegur, Service,
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pers. obs., 2013). On the island of
Anegada, numerous invasive plants
have been documented in the town of
The Settlement, three of which have
been observed moving towards natural
habitats (McGowan et al. 2006, p. 4),
further promoting the risk of wildfires
that can affect V. rupicola.
With respect to Agave eggersiana, the
populations at Protestant Cay, Gallows
Bay, and Great Pond are surrounded by
dense stands of different species of
Sansevieria, an herb native to Africa.
This invasive species seems to be
occupying the ecological niche adjacent
to known populations of A. eggersiana
(O. Monsegur, Service, pers. obs., 2013).
This invasive species can constrain the
number of individuals of A. eggersiana
and reduce the species’ limited
populations even more.
Gonocalyx concolor
Invasive, native plants, such as the
ferns Gleichenella pectinata and
Sticherus bifidus, may invade and alter
diverse native communities, often
resulting in plant monocultures that
support few wildlife species (Walker et
al. 2010, p. 627). These ferns can
colonize disturbed areas faster than
other native plants and may grow into
dense mats, thereby excluding native
plants (Walker et al. 2010, p. 634).
Additionally, the mats formed by these
species serve as fuel for fires and, in
fact, seems to be fire-tolerant. The
invasive, nonnative grass Pennisetum
purpureum (elephant grass) is a fireadapted species that, in dense growth,
can suppress most grasses, herbs, and
tree seedlings (J. K. Francis, ITF,
internet data, 2013).
These invasive ferns and grass are
currently found occupying areas
disturbed by fire, landslides, and road
construction in Cerro La Santa, and
have the potential to affect Gonocalyx
concolor by increasing fire incidences,
microclimate, and nutrient cycling of
the habitat on which this species
depends. At present, we have no
information about the competitive
abilities of G. concolor in such a
situation. Therefore, the effect of
invasive species within the G. concolor
habitat should be considered a threat to
the species.
Human-Induced Fires
Fire is not a natural event in
subtropical dry or moist forests in
Puerto Rico and the U. S. Virgin Islands.
The vegetation in the Caribbean is not
adapted to fires, because this
disturbance does not naturally occur on
these islands (Brandeis and Woodall
´
2008, p. 557; Santiago-Garcıa et al.
2008, p. 604). Human-induced fires
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62573
could modify the landscape by
promoting nonnative trees and grasses,
and by diminishing the seed bank of
native species (Brandeis and Woodall
2008, p. 557). In some cases, fires may
maintain extensive areas of young forest
and grasslands, slowing the recovery of
ecosysems and, therefore, impairing the
delivery of ecosystem services (Brandeis
and Woodall 2008, p. 557). For example,
the nonnative Megathyrsus maximus is
well adapted to fires and typically
colonizes areas that were previously
covered by native vegetation.
Furthermore, the presence of this
species increases the amount of fuel and
the intensity of fires. Therefore, damage
caused by fires to the ecosystems,
particularly to juvenile plants, might be
irreversible.
Varronia rupicola and Agave eggersiana
Human-induced fires may lead to
destruction of the native vegetation seed
bank and may create conditions
favorable for the establishment of
nonnative plant species adapted to fires
(e.g., Leucaena leucocephala and
Megathyrsus maximus) that may
outcompete Varronia rupicola and
Agave eggersiana. Furthermore, the
presence of M. maximus and other grass
species increases the amount of fuel and
the intensity of fires that may affect
endemic populations. Seedling
mortality after fires is related to the
differences on fuel loads and the
´
different fire intensities (Santiago-Garcıa
et al. 2008, p. 607). The V. rupicola
populations that occur along the
˜
municipalities of Yauco, Penuelas, and
Ponce are susceptible to forest fires,
particularly on private lands where fires
are accidentally or deliberately ignited.
Evidence of recent fires within the
habitat and adjacent to known
˜
populations of V. rupicola in Penuelas
and Ponce have been observed by
Service biologist Omar Monsegur (2011
and 2013). Varronia rupicola
´
populations within the Guanica
Commonwealth Forest may be
protected, as this conservation area has
an active fire control program (M.
Canals, DNER, pers. comm. 2008).
´
Nonetheless, Miguel Canals, Guanica
Commonwealth Forest Manager,
indicates that fires still occur in the
forest, particularly on the periphery
along roads (Canals, DNER, pers. comm.
2008). Moreover, accidental fires have
been reported below the PREPA power
lines adjacent to known populations of
V. rupicola.
On the island of St. Croix, humaninduced fires are also frequently
reported, and most of them appear to
have been originated close to existing
roads (Chakroff 2010, p. 41). Estate
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Granard, Estate Jack’s Bay, and Estate
Isaacs Bay are among the areas
identified as fire hotspots (Chakroff
2010, p. 42). One of the extant
populations of Agave eggersiana is
found on Estate Granard, and Jack’s Bay
and Isaacs Bay Estates are within the
historical range for the species. In fact,
from 2006 to 2009, there were between
1 and 6 fires in these estates (Chakroff
2010, p. 42). Human-induced fires
particularly threaten the A. eggersiana
population at Great Pond due to the
abundance of nonnative grasses in this
area. Service’s personnel in St. Croix
just documented a wild fire affecting the
population of Catesbaea melanocarpa
(Claudia Lombard, Service, pers. comm.
2013). This population is located less
than 0.3 mi (0.5 km) from the A.
eggersiana population at Manchenil
Bay.
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Gonocalyx concolor
Human-induced fire is also a current
threat to Gonocalyx concolor at Cerro La
Santa. Areas adjacent to (less than 33 ft
(10 m) from) a population of this species
have been affected by such fires (O.
Monsegur, UPRM, unpubl. data, 2006).
Fire effects could accelerate the
colonization of invasive plants and
change the vegetation composition of
Cerro La Santa (see discussion under
Factor A, above). Currently, Pennisetum
purpureum, a nonnative grass, is
occupying these areas, making them
vulnerable to human-induced fires.
During the dry season (March through
May), the fern Gleichenella pectinata,
and other fern species that have
colonized landslides and roadsides,
form dense mats of dry material that
serve as fuel for fires. Although Cerro La
Santa is located in the wet forest, fires
still occur in the area, particularly along
roads, during the dry season (C.
Pacheco, USFWS, pers. obs. 2013). Due
to the small size of G. concolor
populations and their proximity to areas
susceptible to human-induced fires, the
Service considers habitat modification
by fires as a threat to the species.
Hurricanes and Climate Change
The islands of the Caribbean are
frequently affected by hurricanes. The
U.S. Virgin Islands have been hit by five
major hurricanes in recent years: Hugo
(1989), Luis and Marilyn (1995), Lenny
(1999), and Omar (2008). Examples of
the visible effects of hurricanes on the
ecosystem include massive defoliation,
snapped and wind-thrown trees, large
debris accumulations, landslides, debris
flows, altered stream channels, and
transformed beaches (Lugo 2008, p.
368). Successional responses to
hurricanes can influence the structure
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and composition of plant communities
in the Caribbean islands (Van Bloem et
al. 2003, p. 137; Van Bloem et al. 2005,
p. 572; Van Bloem et al. 2006, p. 517;
Lugo 2000, p. 245). Hurricanes can
produce sudden and massive tree
mortality, which is variable among
species (Lugo 2000, p. 245). As
endemics to the Caribbean, Varronia
rupicola, Agave eggersiana, and
Gonocalyx concolor would be expected
to be well adapted to tropical storms
and the prevailing environmental
conditions in this geographical area.
However, the resilience of rare and
endangered native species populations
may be limited or constricted by the
reduced number of populations and
individuals, making the populations
vulnerable to stochastic events.
Varronia rupicola and Agave eggersiana
The reduced number and small size of
Varronia rupicola and Agave eggersiana
populations in Puerto Rico and St.
Croix, respectively, make these species
susceptible to hurricanes impacts (e.g.,
extirpation). In the case of A.
eggersiana, the impacts may be
exacerbated by the reproductive biology
of the species (i.e., the species depends
on asexual reproduction, plants dying
after flowering, and limited dispersal of
bulbils). Therefore, impacts to a
population may compromise its natural
recruitment. In addition, for V. rupicola,
a severe hurricane could result in
extensive defoliation and could cause
stem damage.
Populations of Varronia rupicola may
be threatened by climate change, which
is predicted to increase the frequency
and strength of tropical storms and can
cause severe droughts (Hopkinson et al.
2008, p. 260). Rather than assessing
climate change as a single threat, we
examined the potential consequences to
species and their habitats that arise from
changes in environmental conditions
associated with various aspects of
climate change. For example, climaterelated changes to habitats or conditions
that exceed the physiological tolerances
of a species, occurring individually or in
combination, may affect the status of a
species. In fact, vulnerability to climate
change impacts is a function of
sensitivity, exposure, and adaptive
capacity of species (IPCC 2007, p. 89;
Glick and Stein 2010, p. 19). For
instance, severe droughts may
compromise seedling recruitment, as
they may result in deaths of small
plants, or may compromise the viability
of seeds. Despite the wide distribution
of V. rupicola and the number of
populations, the number of individuals
per population may be too low to
sustain a positive recruitment of
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individuals. This may explain the low
number of intermediate-sized,
nonreproductive individuals of V.
´
rupicola observed in Guanica and
Ponce, when compared to the high
numbers of young seedlings (Omar A.
Monsegur, Service, pers. obs. 2013).
On the island of Anegada, climateinduced sea-level rise could lead to the
extirpation of Varronia rupicola. The
preferred habitat of this species on that
island is in lower elevations, and more
than 40 percent of the island is less than
9.8 ft (3 m) above sea level (Wenger et
al. 2010, p. 8). Similarly, Agave
eggersiana occurs very close to beach
areas in coastal areas. At least two A.
eggersiana populations are located on a
coastal cliff, susceptible to coastal
erosion and landslides. Therefore, we
believe that cyclonic surges and coastal
erosion associated with hurricanes may
significantly affect the populations
located along the coastal areas of St.
Croix (i.e., Manchenil Bay, South Shore,
Cane Garden, Vagthus Point, and
Protestant Cay), due to their proximity
to cliffs and the shoreline.
Gonocalyx concolor
The limited distribution and low
number of populations (3) and
individuals (172 historically reported)
of this species may exacerbate its
vulnerability to natural events such as
hurricanes and landslides, and
compromise its continued existence.
Damage to higher elevation forested
habitat is usually greater during
hurricane events (Weaver 2008, p. 150).
Gonocalyx concolor is extremely
vulnerable due to its habitat
requirements and the fact that it is
usually found growing on the canopy of
the tallest trees in Cerro La Santa and
Charco Azul. The species is usually
associated to old trees with abundant
vines and epiphytes that provide
horizontal structure for the colonization
of the species (probably a habitat
requirement for the germination of
seeds). Hurricane winds often lead to
tree defoliation, loss of small and large
branches, and uprooting, resulting in
damage to adjacent trees and understory
vegetation. As a result, gaps are
produced in the vegetation, causing
temporary changes in the understory
microclimate due to high light levels
and temperature (Walker et al. 2010, p.
626). Therefore, damage to the forest
canopy may result in a direct impact to
individuals of G. concolor that may fall
to the ground and probably be
outcompeted by pioneer plant species
that get established during early
successional stages after hurricanes.
The recovery of elfin forest vegetation
after hurricanes is usually slow, and the
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early regeneration process is dominated
by a few species (Weaver 2008, p. 150).
Furthermore, in the absence of
knowledge of the reproductive capacity
and ecological requirements of
Gonocalyx concolor, it is difficult to
predict its recovery after natural events
such as hurricanes and tropical storms,
particularly when the frequency and
intensity of these weather events is
expected to increase with climate
change.
The habitat where Gonocalyx
concolor occurs is susceptible to
landslides during rain events mostly
associated with tropical storms and
hurricanes. Sometimes rainfall reaches
24 in (60 cm) in a single storm event,
causing floods and interacting with
topography and geologic substrate to
induce mass wasting events (e.g.,
landslides; Lugo 2000, p. 246). In 1998,
during Hurricane Georges, a landslide
adversely affected approximately 2 ac
(0.8 ha) of elfin forest at Cerro La Santa
(Hecsor Serrano-Delgado, DNER, pers.
comm. 2013). A massive landslide in
the area where the species occurs would
not only take out individuals of G.
concolor, but would also modify the
habitat necessary for the species and
lead to conditions favoring the
establishment of invasive and weedy
vegetation that may permanently modify
the habitat and outcompete G. concolor
(see invasive species discussion under
Factor E, above). As documented during
Hurricane Georges, and based on the
current conditions of the habitat at
Cerro La Santa and Charco Azul,
landslides are a current threat to this
species. As with Agave eggersiana and
Varronia rupicola (see discussion
above), overall impact and the
cumulative effects of climate change are
also expected to have long-term adverse
effects on G. concolor. Gonocalyx
concolor is considered a species with
very specific ecological requirements
and that occupies biological islands
(i.e., dwarf forests on high elevations of
Puerto Rico). Thus, predicted changes
on the structure of the vegetation due to
climate change may result in the
irreversible extirpation of the prime
habitat for the species.
tkelley on DSK3SPTVN1PROD with PROPOSALS
Low Reproductive Capacity, Highly
Specialized Ecological Requirements,
and Genetic Variation
19:53 Oct 21, 2013
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Conservation Efforts To Reduce Other
Natural or Manmade Factors Affecting
Their Continued Existence
Varronia rupicola
The staff from the Royal Botanical
Garden (KEW) has developed a
germination and cultivation protocol for
Varronia rupicola. KEW is also
conducting studies to determine the
genetic variation within and among
known populations, and the species’
reproductive biology and population
ecology, to develop a management plan
for the species (Hamilton, KEW, pers.
comm. 2012). Further preliminary
germination experiments have been
conducted in Puerto Rico at the
´
nurseries of the Guanica
Commonwealth Forest and the Cabo
Rojo National Wildlife Refuge. The
Service is not aware of any
conservations measure for Agave
eggersiana or Gonocalyx concolor.
Summary of Factor E
Gonocalyx concolor and Agave
eggersiana
Small and isolated populations of rare
plants often display reduced fitness as
reduced reproductive output, seedling
performance, or pollen viability
(Holmes et al. 2008, p. 1031). In the case
of Gonocalyx concolor, little is known
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about its reproductive capacity,
recruitment, and genetic variation. The
low number of individuals per
population of a monoecious species
(both sexes in the same flower), like G.
concolor, suggests it has highly
specialized ecological requirements,
production of viable seeds rarely occurs,
or there is a pollinator limitation.
Despite the ongoing monitoring of the
known population of G. concolor, no
seedling recruitment has been observed
in the wild. Knowing the phenology of
a plant showing limited distribution is
important in understanding the species’
biology and ecology, such as the timing
of flowering, fruiting, germination and
subsequent growth, and accumulation of
biomass in the field (Ruml and Vulic
2005, p. 218). Additionally, given the
extremely limited geographic
distribution of G. concolor, it is likely
that its genetic variability is low.
In the case of Agave eggersiana, its
reproductive biology is characterized by
its dependence on asexual reproduction
(i.e., bulbils). Current evidence suggests
that the wild and cultivated populations
of A. eggersiana have minimum genetic
variation. This would result in the loss
of alleles by random genetic drift, which
would limit the species’ ability to
respond to changes in the environment
(Honnay and Jacquemyn, 2007, p. 824).
Agave eggersiana
Based on the above information and
due to the reduced number of
populations and individuals, we believe
that Agave eggersiana is currently
threatened by natural or manmade
factors, including hurricanes, fires, and
competition with nonnative species.
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Climate change may exacerbate these
habitat threats by increasing the
frequency of fires, droughts, and
hurricanes, but to an unknown extent.
Gonocalyx concolor
The primary threats to Gonocalyx
concolor are its limited distribution and
highly specialized ecological
requirements. Other potential threats
include low reproductive capacity,
possible low genetic variation, effects of
vegetation management, hurricanes and
landslides, human-induced fire, and
climate change. G. concolor is
susceptible to hurricanes, landslides,
and human-induced fire because it is
confined to geographically small areas.
Invasive species and climate change are
potential threats that may be expected
in the future. G. concolor could be
negatively affected by the increasing
intensity and frequency of hurricanes
and tropical storms, environmental
effects resulting from changing climatic
patterns. Any disturbance of vegetation
along the road and around the
telecommunication facilities (including
landslides) where the species is found
may directly impact individuals and
create conditions favorable for the
establishment of invasive species that
may alter (modify) G. concolor habitat.
Varronia rupicola
Varronia rupicola is threatened
primarily by human-induced fires
within its prime habitat. Habitat
modification by urban development has
promoted the invasion of its habitat by
nonnative plant species (e.g., grasses)
that are typically fire-adapted and,
therefore, increase the chances of fires
by providing a higher fuel load in the
ecosystem. Evidence of recent fires has
been documented within the
˜
municipalities of Penuelas and Ponce in
areas close to V. rupicola, threatening
these natural populations. Overall,
nonnative plants and fires may result in
extirpation of populations of V. rupicola
by killing individuals, limiting natural
recruitment, or permanently modifying
habitat and conditions necessary for the
species’ establishment. Furthermore,
due to the species’ limited numbers and
distribution, hurricanes may extirpate
entire populations, and in the case of a
highly fragmented habitat, hurricanes
may further promote the invasion of
forest gaps by nonnative plant species
rather than native pioneers. Similarly,
severe droughts resulting from climate
change may compromise the survival of
seedlings and diminish natural
recruitment within wild populations.
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Cumulative Effects: Factors A through E
Agave eggersiana
The limited distributions and small
population sizes of Agave eggersiana
make this species very susceptible to
further habitat loss (Factor A), diseases
(Factor C), and competition with
nonnative species (Factor E).
Hurricanes, human-induced fires, and
climate changes (Factor E) exacerbate
current threats to the species.
Furthermore, although the species is
protected by territorial law, enforcement
still is a challenge (Factor D), risking the
continued survival of the species. While
these threats may act in isolation, it is
very likely that two or more of these
stressors (e.g., habitat loss and diseases)
act simultaneously or in combination,
resulting in cumulative impacts to
populations of A. eggersiana.
tkelley on DSK3SPTVN1PROD with PROPOSALS
Gonocalyx concolor
The rarity and specialized ecological
requirements of Gonocalyx concolor
(Factor E) make this species extremely
vulnerable to habitat destruction or
modification (Factor A), and to other
natural or manmade factors, such as low
reproductive capacity, possible low
genetic variation, invasive species,
hurricanes, landslides, human-induced
fires, and climate change, particularly
because it is confined to small
geographical areas (Factor E).
Furthermore, implementation and
enforcement of effective measures to
protect G. concolor have not prevented
impacts to the species (Factor D).
Although the above mentioned threats
may act in isolation, it is very likely that
two or more of these stressors act
simultaneously or in combination (e.g.,
hurricanes and landslides; fires and
invasion of nonnative plant species),
resulting in cumulative impacts to
populations of G. concolor, challenging
its recovery.
Varronia rupicola
Varronia rupicola has a somewhat
extended distribution in southern
Puerto Rico. However, the species is
represented by small and fragmented
populations, and about half of them
occur within private lands subject to
urban development, making the species
prone to destruction, modification, or
curtailment of its habitat (Factor A).
Moreover, other natural or manmade
factors such as invasive species, humaninduced fires, hurricanes, and climate
change (Factor E) also pose threats to V.
rupicola. Furthermore, implementation
and enforcement of regulatory
mechanisms to protect the species have
not been effective, particularly because
enforcement on private lands continues
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to be a challenge (Factor D). Therefore,
it is very likely that cumulative effects
of these threats (e.g., poorly
implemented regulatory mechanisms
and habitat destruction) result in
limitation, or even local extirpation, of
V. rupicola populations.
Proposed Determination
Agave eggersiana
Agave eggersiana is highly threatened
by limited habitat and habitat loss (e.g.,
construction of roads, and residential
and tourist developments and
landscaping (Factor A)) and the
potential for a disease to wipe out the
limited populations (Factor C). In
addition, agave is threatened by a high
possibility of commercial collection for
ornamental uses (Factor B), and
competition with invasive, nonnative
plants, as well as hurricanes and
human-induced fires, which are further
exacerbated by climate change (Factor
E). Due to lack of enforcement, existing
regulatory mechanisms are not
adequately reducing these threats
(Factor D). All of these threats currently
occur rangewide and are likely to
continue into the foreseeable future at a
medium to high intensity.
Based on our evaluation of the best
available scientific and commercial
information on the species, the
significant threats affecting Agave
eggersiana and its habitat, as well as
future potential threats, we have
determined the species is in danger of
extinction throughout all of its range. As
a result, we find that A. eggersiana
meets the definition of an endangered
species. We find that a threatened
species status is not appropriate for A.
eggersiana because the species is very
limited in numbers and in populations,
and because threats are current and
ongoing, occurring rangewide, and
expected to continue into the future.
Gonocalyx concolor
Gonocalyx concolor has a very limited
distribution. According to our
assessment, this species is threatened by
habitat destruction or modification
(Factor A) associated with maintenance
and potential expansion of
telecommunication facilities, and to
other natural or manmade factors (i.e.,
low reproductive capacity, possible low
genetic variation, invasive species,
hurricanes, landslides, human-induced
fires, and climate change (Factor E)).
Due ineffective implementation and
enforcement, existing regulatory
mechanisms are not adequately
reducing these threats (Factor D). All of
these threats currently occur rangewide
and are likely to continue into the
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foreseeable future at a medium to high
intensity.
Based on our evaluation of the best
available scientific and commercial
information on the species, the
significant threats affecting Gonocalyx
concolor and its habitat, as well as
future potential threats, we have
determined the species is currently in
danger of extinction throughout all of its
range. As a result, we find that G.
concolor meets the definition of an
endangered species. We find that a
threatened species status is not
appropriate for G. concolor because the
species is already very limited in
numbers and distribution (i.e., it has a
contracted range), and the threats are
current and ongoing, occurring
rangewide, and expected to continue
into the future.
Varronia rupicola
Current evidence indicates that the
majority of suitable habitat and known
populations of Varronia rupicola lie
within private lands in southern Puerto
˜
Rico (i.e., Yauco, Penuelas, and Ponce).
These lands are subject to habitat
destruction or modification where
impacts to habitat and populations have
been documented. Furthermore,
´
populations located within the Guanica
Commonwealth Forest have been
affected by management practices, such
as trail and power lines maintenance
(Factor A). Habitat destruction further
results in the intrusion of nonnative
plant species that have the potential to
outcompete V. rupicola and create
favorable conditions for fire (Factor E).
Furthermore, implementation and
enforcement of regulatory mechanisms
to protect the species have not been
effective in reducing these threats,
particularly because enforcement on
private lands continues to be a
challenge (Factor D). Some of these
threats are occurring presently at a
moderate level, and are likely to
increase in the foreseeable future to a
high intensity.
We have carefully assessed the best
scientific and commercial information
available regarding the past, present,
and future threats to Varronia rupicola,
and have determined that the species
meets the definition of a threatened
species throughout all of its range. We
find that an endangered species status is
not appropriate for V. rupicola because
the species is not currently in danger of
extinction, but likely will be in the
future. It has a wide distribution
throughout the Puerto Rican bank
(geographical unit that includes the
main island of Puerto Rico, Vieques,
Culebra, the USVI (excluding St. Croix)
and the island of Anegada)), has no
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germination problems, develops as
reproductive individuals in a relatively
short time period (1 to 2 years under
nursery conditions), and is the subject
of propagation and conservation
protocols in development by the staff of
the Royal Botanical Garden (KEW).
Therefore, the Service considers that V.
rupicola is a species with a high
recovery potential that meets the
definition of a threatened species.
tkelley on DSK3SPTVN1PROD with PROPOSALS
Significant Portion of the Range
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.’’
A major part of the analysis of
‘‘significant portion of the range’’
requires considering whether the threats
to the species are geographically
concentrated in any way. If the threats
are essentially uniform throughout the
species’ range, then no portion is likely
to warrant further consideration.
Based on the threats to Agave
eggersiana and Gonocalyx concolor
throughout their entire known ranges,
we find that these species currently are
in danger of extinction throughout all of
their ranges, based on the severity and
scope of the threats described above. As
previously discussed, A. eggersiana and
G. concolor are proposed for listing as
endangered species, rather than
threatened species, because the major
threats are occurring now, and
additional threats will impact them in
the near term. The potential impacts to
the species would be severe given their
limited known distribution, the small
population sizes at the remaining sites,
and the small area occupied by most of
the populations. Because the threats
acting over the three species extend
throughout their entire ranges, it is
unnecessary to determine if the species
are in danger of extinction throughout a
significant portion of their ranges. We
find that the threats to Varronia
rupicola are a result of future
development and lack of regulatory
mechanisms. These impacts are not
occurring now. Therefore, on the basis
of the best available scientific and
commercial information, we propose
listing A. eggersiana and G. concolor as
endangered species, and V. rupicola as
threatened species, throughout their
ranges in accordance with sections 3(6)
(endangered), 3(20) (threatened), and
4(a)(1) of the Act.
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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 the species,
results in public awareness and
conservation by Federal, State, Tribal,
and local agencies; private
organizations; and individuals. The Act
encourages cooperation with the States
and requires that recovery actions be
carried out for all listed species. The
protection required by Federal agencies
and the prohibitions against certain
activities are discussed, in part, below.
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Subsection 4(f) of
the Act requires the Service to develop
and implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse the species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, 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 identifies site-specific
management actions that set a trigger for
review of the five factors that control
whether a species remains endangered
or may be downlisted or delisted, and
methods for monitoring recovery
progress. Recovery plans also establish
a framework for agencies to coordinate
their recovery efforts and provide
estimates of the cost of implementing
recovery tasks. Recovery teams
(composed of species experts, Federal
and State agencies, nongovernmental
organizations, and stakeholders) are
often established to develop recovery
plans. When completed, the recovery
outline, draft recovery plan, and the
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62577
final recovery plan will be available on
our Web site (https://www.fws.gov/
endangered), or from our Caribbean
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Implementation of recovery actions
generally requires the participation of a
broad range of partners, including other
Federal agencies, States, Tribes,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private and Commonwealth and
Territory lands.
If these species are listed, funding for
recovery actions will be available from
a variety of sources, including Federal
budgets, State programs, and cost share
grants for non-Federal landowners, the
academic community, and
nongovernmental organizations. In
addition, pursuant to section 6 of the
Act, the Territory of the U.S. Virgin
Islands and the Commonwealth of
Puerto Rico would be eligible for
Federal funds to implement
management actions that promote the
protection or recovery of Agave
eggersiana, Gonocalyx concolor, and
Varronia rupicola. Information on our
grant programs that are available to aid
species recovery can be found at: https://
www.fws.gov/grants.
Although Agave eggersiana,
Gonocalyx concolor, and Varronia
rupicola are only proposed for listing
under the Act at this time, please let us
know if you are interested in
participating in recovery efforts for 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
recovery planning purposes (see FOR
FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is 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
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Federal Register / Vol. 78, No. 204 / Tuesday, October 22, 2013 / Proposed Rules
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 formal
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 (Vieques National
Wildlife Refuge), and National Park
Service (SARI and Buck Islands
Monument); issuance of section 404
Clean Water Act (33 U.S.C. 1251 et seq.)
permits by the U.S. Army Corps of
Engineers; and construction and
maintenance of roads or highways by
the Federal Highway Administration.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to endangered and threatened plants.
The prohibitions of section 9(a)(2) of the
Act, codified at 50 CFR 17.61, apply to
endangered plants. These prohibitions,
in part, make it illegal for any person
subject to the jurisdiction of the United
States to import or export, transport in
interstate or foreign commerce in the
course of a commercial activity, sell or
offer for sale in interstate or foreign
commerce, or remove and reduce the
species to possession from areas under
Federal jurisdiction. In addition, for
plants listed as endangered, the Act
prohibits the malicious damage or
destruction on areas under Federal
jurisdiction and the removal, cutting,
digging up, or damaging or destroying of
such plants in knowing violation of any
State law or regulation, including State
criminal trespass law. It is also unlawful
to violate any regulation pertaining to
plant species listed as endangered or
threatened (section 9(a)(2)(E) of the Act).
We may issue permits to carry out
otherwise prohibited activities
involving endangered and threatened
species under certain circumstances.
Regulations governing permits are
codified at 50 CFR 17.62 for endangered
plants, and at 17.72 for threatened
plants. With regard to endangered
plants, a permit must be issued for the
following purposes: for scientific
purposes or to enhance the propagation
or survival of the species.
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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.
The following activities could
potentially result in a violation of
section 9 of the Act; this list is not
comprehensive:
(1) Unauthorized collecting, handling,
possessing, selling, delivering, carrying,
or transporting of Agave eggersiana,
Gonocalyx concolor, or Varronia
rupicola, including import or export
across State lines and international
boundaries, except for properly
documented antique specimens of these
taxa at least 100 years old, as defined by
section 10(h)(1) of the Act;
(2) Introduction of nonnative species
that compete with or prey upon Agave
eggersiana, such as the introduction of
the nonnative agave snout weevil to the
island of St. Croix, USVI; and
(3) The unauthorized release of
biological control agents that attack any
life stage of Agave eggersiana,
Gonocalyx concolor, or Varronia
rupicola.
Questions regarding whether specific
activities would constitute a violation of
section 9 of the Act should be directed
to the Caribbean Ecological Services
Field Office (see FOR FURTHER
INFORMATION CONTACT).
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. We have
invited these peer reviewers to comment
during this public comment period.
We will consider all comments and
information we receive during the
comment period on this proposed rule
during our preparation of a final
determination. Accordingly, the final
decision may differ from this proposal.
Public Hearings
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
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sent to the address shown in the FOR
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.
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
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 (42
U.S.C. 4321 et seq.)
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act
(NEPA), 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 Caribbean
Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Authors
The primary authors of this proposed
rule are the staff members of the
Caribbean Ecological Services Field
Office.
E:\FR\FM\22OCP1.SGM
22OCP1
62579
Federal Register / Vol. 78, No. 204 / Tuesday, October 22, 2013 / Proposed Rules
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
50 of the Code of Federal Regulations,
as set forth below:
2. Amend § 17.12(h) by adding entries
for Agave eggersiana, Gonocalyx
concolor, and Varronia rupicola, in
alphabetical order under FLOWERING
PLANTS, to the List of Endangered and
Threatened Plants to read as follows:
■
PART 17—[AMENDED]
Proposed Regulation Promulgation
1. The authority citation for part 17
continues to read as follows:
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
Authority: 16 U.S.C. 1361–1407; 1531–
1544; 4201–4245, unless otherwise noted.
■
§ 17.12
*
Endangered and threatened plants.
*
*
(h) * * *
Species
*
When
listed
Historic range
Family
*
*
*
Agave eggersiana ................ None ....................................
*
U.S.A. (VI) ......
*
Agavaceae ......
E
*
*
*
Gonocalyx concolor .............. None ....................................
*
U.S.A. (PR) .....
*
Ericaceae ........
E
*
*
*
Varronia rupicola .................. None ....................................
*
U.S.A. (PR);
British VI.
*
Boraginaceae
T
Scientific name
Status
Common name
*
Critical
habitat
Special
rules
FLOWERING PLANTS
*
*
*
*
*
*
*
*
Dated: September 3, 2013.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. 2013–22742 Filed 10–3–13; 8:45 am]
BILLING CODE 4310–55–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 622
[Docket No. 130710605–3605–01]
RIN 0648–BD41
Fisheries of the Caribbean, Gulf of
Mexico, and South Atlantic; Shrimp
Fishery of the Gulf of Mexico;
Establish Funding Responsibilities for
the Electronic Logbook Program
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed changes to
management measures; request for
comments.
tkelley on DSK3SPTVN1PROD with PROPOSALS
AGENCY:
NMFS proposes to establish
funding responsibilities for an upgrade
to the shrimp electronic logbook (ELB)
program as described in a framework
action to the Fishery Management Plan
for the Shrimp Fishery of the Gulf of
Mexico (FMP), as prepared by the Gulf
of Mexico (Gulf) Fishery Management
SUMMARY:
VerDate Mar<15>2010
19:53 Oct 21, 2013
Jkt 232001
*
Written comments must be
received on or before November 6, 2013.
DATES:
You may submit comments
on the proposed changes to the
management measures, identified by
‘‘NOAA–NMFS–2013–0127’’ by any of
the following methods:
• Electronic Submission: Submit all
electronic public comments via the
Federal e-Rulemaking Portal. Go to
www.regulations.gov/
#!docketDetail;D=NOAA-NMFS-20130127, click the ‘‘Comment Now!’’ icon,
complete the required fields, and enter
or attach your comments.
ADDRESSES:
Frm 00108
Fmt 4702
Sfmt 4702
*
NA
*
NA
*
NA
*
*
Council (Council). Newer and more
efficient ELB units have been purchased
by NMFS for the Gulf shrimp fleet and
are available for installation on Gulf
shrimp vessels. If the framework action
is implemented, the proposed changes
to the management measures would
include establishing a cost-sharing
program to fund the ELB program. The
proposed changes would require NMFS
to pay for the software development,
data storage, effort estimation analysis,
and archival activities for the new ELB
units, and vessel permit holders in the
Gulf shrimp fishery to pay for
installation and maintenance of the new
ELB units and for the data transmission
from the ELB units to a NOAA server.
The purpose of the proposed changes is
to ensure that management of the
shrimp fishery is based upon the best
scientific information available and that
bycatch is minimized to the extent
practicable.
PO 00000
*
NA
*
NA
*
NA
*
• Mail: Submit written comments to
Susan Gerhart, Southeast Regional
Office, NMFS, 263 13th Avenue South,
St. Petersburg, FL 33701.
Instructions: Comments sent by any
other method, to any other address or
individual, or received after the end of
the comment period, may not be
considered by NMFS. All comments
received are a part of the public record
and will generally be posted for public
viewing on www.regulations.gov
without change. All personal identifying
information (e.g., name, address, etc.),
confidential business information, or
otherwise sensitive information
submitted voluntarily by the sender will
be publicly accessible. NMFS will
accept anonymous comments (enter
‘‘N/A’’ in the required fields if you wish
to remain anonymous). Attachments to
electronic comments will be accepted in
Microsoft Word, Excel, or Adobe PDF
file formats only.
Electronic copies of the framework
action, which includes a Regulatory
Flexibility Act analysis and a regulatory
impact review, may be obtained from
the Southeast Regional Office Web site
at https://sero.nmfs.noaa.gov/
sustainable_fisheries/gulf_fisheries/
shrimp/.
Comments regarding the burden-hour
estimates or other aspects of the
collection-of-information requirements
contained in the proposed changes to
the management measures may be
submitted in writing to Anik Clemens,
Southeast Regional Office, NMFS, 263
13th Avenue South, St. Petersburg, FL
E:\FR\FM\22OCP1.SGM
22OCP1
Agencies
[Federal Register Volume 78, Number 204 (Tuesday, October 22, 2013)]
[Proposed Rules]
[Pages 62560-62579]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-22742]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R4-ES-2013-0103; 4500030113]
RIN 1018-AZ10
Endangered and Threatened Wildlife and Plants; Endangered Status
for Agave eggersiana and Gonocalyx concolor, and Threatened Status for
Varronia rupicola
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), propose to
list Agave eggersiana (no common name) and Gonocalyx concolor (no
common name) as endangered species, and Varronia rupicola (no common
name) as a threatened species under the Endangered Species Act of 1973,
as amended (Act). These three plants are endemic to the Caribbean. The
effect of this regulation, if finalized, would be to conserve A.
eggersiana, G. concolor, and V. rupicola under the Act.
DATES: We will accept comments received or postmarked on or before
December 23, 2013. Comments submitted electronically using the Federal
eRulemaking Portal (see ADDRESSES section, below) must be received by
11:59 p.m. Eastern Time on the closing date. We must receive requests
for public hearings, in writing, at the address shown in FOR FURTHER
INFORMATION CONTACT by December 6, 2013.
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-2013-0103,
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-2013-0103; Division of Policy and
Directives Management; U.S. Fish and Wildlife Service; 4401 N. Fairfax
Drive, MS 2042-PDM; Arlington, VA 22203.
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 the Information Requested section below for more information).
FOR FURTHER INFORMATION CONTACT: Marelisa Rivera, Deputy Field
Supervisor, U.S. Fish and Wildlife Service, Caribbean Ecological
Services Field Office, P.O. Box 491, Road 301 Km. 5.1, Boquer[oacute]n,
PR 00622; by telephone 787-851-7297; or by facsimile 787-851-7440.
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 intend to list
a species as endangered or threatened throughout all or a significant
portion of its range, we are required to promptly publish a proposal in
the Federal Register and make a final determination on our proposal
within 1 year. Listing a species as an endangered or threatened species
can only be completed by issuing a rule. Agave eggersiana, Gonocalyx
concolor, and Varronia rupicola are 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 proposal has until now been precluded by other higher
priority listing activities.
This rule consists of a proposed rule to list Agave eggersiana and
Gonocalyx concolor as endangered, and Varronia rupicola as threatened.
This proposed rule reassesses all available information regarding the
status of and threats to A. eggersiana, G. concolor, and V. rupicola.
Elsewhere in today's Federal Register, we propose to designate critical
habitat for A. eggersiana, G. concolor, and V. rupicola under the Act.
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 listing is warranted for these species,
which are currently at risk throughout all of their respective ranges
due to threats related to:
A. eggersiana--potential future development for
residential, urban, and tourist use; agriculture use; dropping of
debris; competing nonnative plants; fires; predation; and disease cause
by insects (weevils).
G. concolor--installation or expansion of
telecommunication towers, road improvement, vegetation management, and
small number of individuals and populations.
V. rupicola--loss of habitat due to urban development,
right-of-way development and maintenance, deforestation, and
hurricanes; and inadequate existing regulatory mechanisms (lack of
enforcement).
We will seek peer review. We are seeking comments from
knowledgeable individuals with scientific expertise to review our
analysis of the best available science and application of that science
and to provide any additional information to improve this proposed
rule. Because we will consider all comments and information we receive
during the comment period, our final determinations may differ from
this proposal.
Information Requested
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 biology, range, and population trends of A. eggersiana, G.
concolor, and V. rupicola, including:
(a) Habitat requirements for feeding, reproducing, and sheltering;
(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 these species, their
habitat, or both.
(2) The factors that are the basis for making a listing
determination for these
[[Page 62561]]
species under section 4(a) of the Act, which are:
(a) The present or threatened destruction, modification, or
curtailment of their 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 their continued
existence.
(3) Biological, commercial trade, or other relevant data concerning
any threats (or lack thereof) to these species and existing regulations
that may be addressing those threats.
(4) Additional information concerning the historical and current
status, range, distribution, and population size of these species,
including the locations of any additional populations of these species.
(5) Any information on the biological or ecological requirements of
the species and ongoing conservation measures for the species and their
habitats.
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 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.
Please include sufficient information with your comments to allow us to
verify any scientific or commercial information you include.
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, Caribbean Ecological Services Field Office (see FOR
FURTHER INFORMATION CONTACT).
Previous Federal Actions
Through February 1996
On December 15, 1980, Agave eggersiana, Gonocalyx concolor, and
Varronia rupicola (as Cordia rupicola) were identified as Category 2
candidate species in the candidate notice of review (CNOR) published in
the Federal Register (45 FR 82480). A Category 2 species was one for
which the Service had information that proposing as endangered or
threatened may be appropriate but for which sufficient information was
not currently available to support a proposed rule. None of the three
species was mentioned in the November 28, 1983, CNOR (48 FR 53640), but
all three again were named as Category 2 candidate species in the
September 27, 1985, CNOR (50 FR 39526). They all remained Category 2
candidate species in the February 21, 1990 (55 FR 6184), and September
30, 1993 (58 FR 51144), CNORs. Designation of Category 2 species was
discontinued in the February 28, 1996, CNOR (61 FR 7596). The 1996 CNOR
redefined candidates to include only species for which we have
information needed to propose them for listing, and as a result, A.
eggersiana, G. concolor, and V. rupicola were removed from the
candidate list.
After February 1996: Agave eggersiana
On November 21, 1996, we received a petition from the U.S. Virgin
Islands Department of Planning and Natural Resources (DPNR) requesting
that we list Agave eggersiana as endangered. On November 16, 1998, we
published in the Federal Register (63 FR 63659) our finding that the
petition to list A. eggersiana presented substantial information
indicating that the requested action may be warranted, and we initiated
a status review on the plant.
On September 1, 2004, the Center for Biological Diversity (CBD)
filed a lawsuit against the Department of the Interior and the Service
alleging that the Service failed to publish a 12-month finding for
Agave eggersiana (Center for Biological Diversity v. Norton, Civil
Action No. 1:04-CV-2553 CAP). In a stipulated settlement agreement
resolving that case, signed April 27, 2005, we agreed to submit our 12-
month finding for A. eggersiana to the Federal Register by February 28,
2006. On March 7, 2006, we published our 12-month finding (71 FR 11367)
that listing of A. eggersiana was not warranted. On September 9, 2008,
CBD filed a complaint that challenged our 12-month finding (Center for
Biological Diversity v. Hamilton, Case No. 1:08-cv-02830-CAP). In a
settlement agreement approved by the Court on August 21, 2009, the
Service agreed to submit to the Federal Register a new 12-month finding
for A. eggersiana. On September 22, 2010, we published in the Federal
Register (75 FR 57720) a finding that listing A. eggersiana was
warranted, but precluded by higher priority actions to amend the Lists
of Endangered and Threatened Wildlife and Plants.
Agave eggersiana was named a candidate species with a listing
priority number (LPN) of 8 in the CNORs published on November 10, 2010
(75 FR 69222), October 26, 2011 (76 FR 66370), and November 21, 2012
(77 FR 69993). An LPN of 8 was assigned to Agave eggersiana because the
species faced threats of moderate magnitude that were imminent.
After February 1996: Gonocalyx concolor and Varronia rupicola
On October 25, 1999, we published in the Federal Register a CNOR
(64 FR 57535) that added Gonocalyx concolor and Varronia rupicola (as
Cordia rupicola) to the list of candidate species with LPNs of 5 and 2,
respectively. Gonocalyx concolor was assigned an LPN of 5 because it
faced threats that were high in magnitude but nonimminent. Varronia
rupicola (as Cordia rupicola) was assigned an LPN of 2 because it faced
threats of a high magnitude that were imminent. These two plants
retained their respective LPN assignments in the CNORs published 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), and September 12, 2006
(71 FR 53756).
In the CNOR published on December 6, 2007 (72 FR 69034), Varronia
rupicola (as Cordia rupicola) was assigned an LPN of 5, because its
threats were determined to be nonimminent. In the 2007 CNOR, Gonocalyx
concolor retained its LPN of 5. Both plants retained an LPN of 5 in the
CNORs published on December 10, 2008 (73 FR 75176), November 9, 2009
(74 FR 57804), November 10, 2010 (75 FR 69222), October 26, 2011 (76 FR
66370), and November 21, 2012 (77 FR 69993).
On May 11, 2004, we received a petition from the CBD (CBD 2004, pp.
[[Page 62562]]
66-69) requesting that G. concolor and V. rupicola be listed as an
endangered species under the Act. No new information was provided in
the petition.
Species Information
Taxonomy and Description
Agave eggersiana
Agave eggersiana is a flowering plant of the family Agavaceae
(century plant family) endemic to the island of St. Croix in the U.S.
Virgin Islands (USVI). This species was originally described in 1913,
by William Trelease from material collected on St. Croix, and is
distinguished from other members of the Agavaceae family by its
acaulescent (without an evident leafy stem), non-suckering growth habit
(vegetative reproduction that does not form offshoots around its base),
and its fleshy, nearly straight leaves with small marginal prickles of
0.04 inches (in) (0.1 centimeters (cm)) long that are nearly straight
(Britton and Wilson 1923, p. 156; Proctor and Acevedo-Rodr[iacute]guez
2005, p. 118). Its flowers are deep yellow and 2.0 to 2.34 in (5 to 6
cm) long. After flowering, the panicles (inflorescence) produce
numerous small vegetative bulbs (bulbils), from which the species can
be propagated (Proctor and Acevedo-Rodr[iacute]guez 2005, p. 118).
Agave eggersiana is not known to produce fruit, and like other Agave
species, is monocarpic, meaning the plant dies after producing the
spike or inflorescence. Furthermore, based on observations of
cultivated plants, A. eggersiana requires at least 10 to 15 years to
develop as a mature individual and to produce an inflorescence (David
Hamada, St. George Village Botanical Garden, pers. comm., 2010).
Gonocalyx concolor
Gonocalyx concolor was described in 1970, as a new species of the
genus Gonocalyx, family Ericaceae, for Puerto Rico (Nevling 1970, p.
221). Gonocalyx is a neotropical genus comprised of 10 species, ranging
from Costa Rica to North Colombia, and the Caribbean (Dominican
Republic, Puerto Rico, Dominica, and Guadalupe) (Luteyn and Pedraza-
Pe[ntilde]alosa 2011, p. 1). Two of the species are considered endemic
to Puerto Rico: G. concolor and G. portoricensis (Lioger and Martorell
2000, p. 151). These two species are derived from common ancestral
stock; hence there is great similarity in many details and in aspect,
as well as geographic proximity (Nevling 1970, p. 223).
Although G. concolor is similar to G. portoricensis, differences in
distribution and flower morphology indicate that they are well-
differentiated species (Nevling 1970, p. 224). The flower of G.
portoricensis is pendent with light green calyx, and the corolla tube
is whitish to pinkish; G. portoricensis is insect-pollinated flower
(Proctor 1992, p. 3). Gonocalyx concolor differs from G. portoricensis
in its vivid red, semipendent flowers, which apparently are hummingbird
pollinated, and in its range (Nevling 1970, p. 224). Gonocalyx concolor
is a small evergreen shrub, mainly epiphytic (grow on the trunks of
trees) or clambering (use other vegetation as support), which may reach
15 feet (ft) (4.7 meters (m)) in length (Acevedo 2005, p. 227). The
leaves are simple, alternate, entire, and coriaceous (leathery). The
leaf blade is ovate, broadly elliptic, or nearly orbicular; 0.5 to 1.2
in (1.5 to 3 cm) long; and 0.5 to 0.9 in (1.3 to 2.3 cm) broad. The
leaf base is apiculate (ending in a short sharp point) and obtuse to
acute at the apex, and is rounded at the base; the leaf's upper surface
is glabrous (smooth or hairless) above, with scattered large trichomes
(papilliform hairs) beneath. The leaf venation is 5-pli (the leaf
venation is 1 central vein and 4 secondary veins bending toward apex)
from the base (secondary veins bending toward apex), outer set
marginal, inner set submarginal and better developed. The mid-vein is
immersed above and emerged beneath, and lateral venation is
inconspicuous. The leaf margin is entire or flat, except for few
inconspicuous, rounded projections toward the apex. The leaf lower
surface is pale green and shiny. The petiole (the stalk attaching the
leaf blade to the stem) is approximately 0.07 to 0.09 in (0.18 to 0.21
cm) long. The stems are highly branched, slender, cylindrical, and dark
brown in color. The twigs are pubescent (covered with fine short
hairs). Young leaves and branches are brilliantly rose-colored, but
become green with age.
Flowers are bisexual, 5-merous (floral part in multiples of 5 in
each whorl), regular, and uniformly vivid red. Flowers are borne
solitary on auxillary brachyblast (short shoot), and are semipendent
(hanging or suspended). Pedicel is terete (cylindrical and tapering),
0.35 to 0.43 in (0.89 to 1.1 cm) long, red, fringed with trichomes at
the summit, bibracteolate (2 bracts subtending the flower within an
inflorescence) near the base, and articulate with calyx. The corolla
(the part of a flower that consists of the separate or fused petals and
constitutes the inner whorl of the perianth) tube is carnose (of a
fleshy consistence), campanulate (shape like a bell), and about 0.5 to
0.6 in (1.3 to 1.5 cm) in length and 0.2 to 0.3 in (0.5 cm to 0.8 cm)
in diameter.
Fruit is a bright red berry with many seeds inside (Lioger 1995, p.
105). No additional information regarding fruit production is
available.
Varronia rupicola
Varronia was traditionally lumped into the genus Cordia, a group of
about 250 or more species of trees and shrubs of tropical and
subtropical regions. Varronia was recently recognized as a monophyletic
genera based on vegetative, floral, and pollen morphology (Miller and
Gottschling 2007, p. 163). Varronia comprises multi-stemmed shrubs with
condensed inflorescence and evenly serrate leaves (S[aacute]nchez de
Stapf 2010, p. 133). Varronia is currently represented in the West
Indies by about 66 valid species (Acevedo-Rodr[iacute]guez and Strong
2012, p. 170). Axelrod (2011, p. 427) recognized seven species found in
Puerto Rico, with V. bellonis and V. wagnerorum being endemic to the
island, and V. rupicola extending to the island of Anegada, British
Virgin Islands.
Varronia rupicola is a large shrub reaching up to 16 ft (5 m) in
height. The alternate leaves are ovate to elliptic, 0.8 to 3.5 in (2 to
9 cm) long with an acute apex, rounded to obtuse at the base, and
chartaceous (papery). Leaves margins are whole or crenate (scalloped or
notched). The upper surface of the leaf is rigidly scabrous (having a
rough surface) and puberulous (densely covered by hairs) underneath,
with strigose (having straight hairs) petioles ranging from 0.1 to 0.4
in (0.2 to 1.0 cm) long. Flowers are in solitary globular heads of 20
(grouped into a globose terminal structure), and about 0.4 in (1.0 cm)
in diameter. The corolla is white and 0.3 in (0.8 cm) long, and the
fruit is a one-seeded, red drupe about 0.2 in (0.5 cm) long (Proctor
1991, p. 65; Lioger 1995, p. 313).
Habitat
Agave eggersiana
Agave eggersiana is currently known from coastal cliffs with sparse
vegetation and dry coastal shrubland vegetation communities within the
subtropical dry forest life zone of St. Croix, USVI (Ewel and Whitmore
1973, p. 72). In St. Croix, the average rainfall is about 30 in (76 cm)
and 40 in (102 cm) in the east and west sides of the island,
respectively (Ewel and Whitmore 1973 p. 8; Mac et al. 1998, p. 315).
The wettest and hottest months are from July to October. The average
mid island temperature is 78.8 degrees
[[Page 62563]]
Fahrenheit ([deg]F) (26 degrees Celsius ([deg]C), with a variation of
only 5 to 9[emsp14][deg]F (3 to 5 [deg]C) between the warmest and
coolest months (Mac et al. 1998, p. 316).
The coastal cliffs where Agave eggersiana occurs are dominated by
rocky formations and areas with less than 10 percent vegetative cover.
These coastal cliffs are exposed to extremes of wind, salt spray, and
low moisture, and they are usually sparsely vegetated with a canopy
less than 1 meter in height (Gibney et al. 2000, p. 7; Moser et al.
2010, Appendix A-11). Dry coastal shrubland vegetation is common to the
drier parts of the island of St. Croix: east and south shores, and low-
elevation locations. In some places, dry coastal shrubland vegetation
may extend as far up as 902 ft (275 m) on south-facing slopes. Cacti
and agave are common though scattered, while vegetation height can
range from 3.2 to 32.8 ft (1 to 10 m). The taller forms may consist of
a canopy layer of larger individuals under slightly more moist
conditions. The shorter forms are common to very exposed locations such
as the east sides of headlands on the south shores in the island
(Gibney et al. 2000, p. 6; Moser et al. 2010, Appendix A-8). Other
species of vegetation associated with these areas are: Sesuvium
portulacastrum (sea purslane), Laguncularia racemosa (white mangrove),
Bucida buceras (black olive), Hippomane mancinella (manchineel),
Jacquinia arborea (barbasco), Opuntia stricta (prickly pear,
Pilosocereus royenii (Royen's tree, Suriana maritima (bay cedar),
Bursera simaruba (gumbo limbo, Canavalia rosea (seaside bean),
Caesalpinia bonduc (gray nicker), Capparis flexuosa (falseteeth),
Scaevola plumieri (ink berry), Oplonia spinosa (prickly bush), Capparis
indica (linguam), Adelia ricinella (wild lime), Crossopetalum rhacoma
(maidenberry, Heteropterys purpurea (bull withe), Pisonia subcordata
(mampoo), Exostema caribaeum (Caribbean princewood, Cordia dentata
(white manjack), and Coccoloba uvifera (seagrape) (O. Monsegur and M.
Vargas, Service, unpubl. data 2013; Lioger and Martorell 2000, pp. 50-
205).
The natural populations of Agave eggesiana grow on top of various
soil classifications, including Cramer, Glynn, Hasselberg, Southgate,
and Victory. The Cramer and Southgate series consists of shallow, well-
drained soils on summits and side slopes of volcanic hills and
mountains. These soils formed in material weathered from extrusive
igneous bedrock or only from igneous bedrock. The Hesselberg series
consists of shallow, well-drained soils on marine terraces. These soils
formed in alkaline, clay sediments. The Glynn series consists of very
deep, well-drained soils on alluvial fans and terraces. These soils
formed in stratified alluvial sediments weathered from basic igneous
rock. The Victory series consists of moderately deep, well-drained
soils on summits and side slopes of volcanic hills and mountains. These
soils formed in material weathered from extrusive igneous bedrock
(USDA-NRCS 2013, https://websoilsurvey.nrcs.usda.gov).
Gonocalyx concolor
Gonocalyx concolor has been described as endemic from the elfin
forest type at Cerro La Santa and from the ausubo (Manilkara bidentata)
forest type at Charco Azul, both within the lower montane (an
altitudinal zone in mountainous region characterized by distinctive
flora and forest structure) very wet forest life zone in the Carite
Commonwealth Forest (Ewel and Whitmore 1973, p. 41). The Carite
Commonwealth Forest comprises approximately 6,694.9 acres (ac) (2,709.3
hectares (ha)), and the elevation ranges from 2,030 to 3,950 ft (620 to
900 m) (DNR 1976, p. 169). This forest has been managed for
conservation since 1975 (DNER 2008, p. 1). The mean annual
precipitation at the Carite Commonwealth Forest is 88.7 in (225 cm),
with February to April the drier months (NOAA 2013, https://www.srh.noaa.gov/sju/?n=climo_cayey).
The mean temperature is 22.7 [deg]C (72.3 [deg]F), varying from 20
[deg]C (68 [deg]F) in January to 24 [deg]C (73.4 [deg]F) in July
(Silander et al. 1986, p. 183).
Both the elfin and ausubo forests have similar climate conditions
(Ewel and Whitmore 1973, p. 32). The elfin forest, also referred to as
dwarf or cloud-forest, is found on exposed peaks and ridges of Cerro La
Santa, above 2,890 ft (880 m) in elevation from sea level, occupying
approximately 10.1 ha (24.9 ac) in the Carite Commonwealth Forest
(Silander et al. 1986, p. 178). The elfin forest vegetation is
characterized by gnarled trees less than 7 meters tall, high basal
area, small diameters, a large number of stems per unit area, and
extremely slow growth rates (Ewel and Whitmore 1973, p. 45). The
vegetation is commonly saturated with moisture and frequently enveloped
in clouds, and both aerial and superficial roots are common (Weaver et
al. 1986, p. 79). The plant association in this area is generally
comprised by few species of native trees, native ferns and dense
covered with epiphytes including bromeliads and mosses (Weaver et al.
1986, p. 79). The native tree composition includes: Tabebuia
schumanniana (roble colorado), Tabebuia rigida (roble de sierra),
Ocotea spathulata (nemoca cimarrona), Eugenia borinquensis (guayabota),
Clusia minor (cupey de monte), and Prestoea acuminata var. montana
(sierra palm) (Weaver et al. 1986, p. 80; Silander et al. 1986, p.
191). Additionally, some areas were planted with Eucalyptus robusta
(swamp mahogany) (O. Monsegur, UPRM, unpubl. report, 2006, p. 1).
The ausubo forest is only found along the R[iacute]o Grande de
Patillas River basin and intermittent streams between 2,034 ft (620 m)
and 2,329.4 ft (720 m) of elevation (DNR 1976, p. 169), and occupying
approximately 72.5 ha (179.2 ac) in the Charco Azul area (Silander et
al. 1986, p. 190). The ausubo forest is characterized by evergreen
vegetation, high species richness, rapid growth rate of successional
trees, epiphytic ferns, bromeliads, and orchids (Ewel and Whitmore
1973, p. 32). The vegetation in this area is generally comprised of
native trees (i.e., Manilkara bidentata (ausubo), Dacryodes excelsa
(tabonuco), Guarea guidonia (guaraguao), and Cyrilla racemiflora (swamp
titi) (Francis and Lowe 2000, p. 345; DNER 2008, p. 2). Gonocalyx
concolor grows epiphytic and clambering on dead and live stand trees
within this type of forest (O. Monsegur, UPRM, unpubl. report, 2006, p.
2).
Varronia rupicola
Varronia rupicola has been described from southwestern Puerto Rico,
Vieques Island, and Anegada Island. All these sites lie within the
subtropical dry forest life zone overlying a limestone substrate (Ewel
and Whitmore 1973, p. 72). Subtropical dry forest life zones receive a
mean annual rainfall ranging from 24 to 40 in (61 to 101 cm). The
vegetation in this life zone is deciduous on most soils, with tree
species dropping leaves during the dry season. The vegetation usually
consists of a nearly continuous, single-layered canopy, with little
ground cover. The leaves of dry forest species are succulent or
coriaceous, and species with spines and thorns are common. Tree heights
usually do not exceed 49 ft (15 m), and crowns are typically broad,
spreading, and flattened (Ewel and Whitmore 1973, p. 72).
Varronia rupicola has been recorded in forested hills with open to
relatively dense shrublands and scrublands 6.5 to 9.8 ft (2 to 3 m) in
height; in low forest with canopy from 8 to 15 ft (3 to 5 m) high; and
at the edge of a dense, low coastal shrubland forest. On the island of
Anegada, V. rupicola was found in open limestone pavement and sand
dunes. Woody species associated to V. rupicola's prime habitat in
southern Puerto Rico (Gu[aacute]nica Commonwealth
[[Page 62564]]
Forest) include: Gymnanthes lucida (shiny oysterwood, or yait[iacute]),
Exostema caribaeum (princewood, or albarillo), Pisonia albida (corcho),
Pictetia aculeata (fustic, or tachuelo), Thouinia portoricensis
(ceboruquillo, or serrazuela), Coccoloba krugii (whitewood),
Pilosocereus royenii (Royen's tree cactus, or sebuc[aacute]n), Bursera
simaruba (gumbo limbo, or almacigo), Erithalis fruticosa (black torch),
Guettarda krugii (frogwood, or cucubano), Tabebuia heterophylla (pink
trumpet tree, or roble), Hypelate trifoliata (inkwood), Coccoloba
diversifolia (pigeonplum, or uvilla), Cassine xylocarpa (marbletree, or
coscorr[oacute]n), Krugiodendron ferreum (black ironwood, or palo de
hierro), Jacquinia berterii (barkwood), Bourreria succulenta
(strongbark, or palo de vaca), Crossopetalum rhacoma (maidenberry, or
pico de paloma), Antirhea acutata (placa chiquitu, or quina), and
Amyris elemifera (torchwood) (Murphy and Lugo 1986, p. 91). The
populations of V. rupicola in Puerto Rico are also found in close
proximity to populations of the endangered plants Eugenia woodburyana
(no common name) and Trichilia triacantha (bariaco), and other rare
plants such as Myrtus bellonis (no common name), Passiflora bilobata
(twolobe passionflower), and Nashia inaguensis (pineapple verbena)
(Breckon and Kolterman 1996, p. 4; Monsegur and Breckon 2007, p. 1). On
Anegada, the species is located in open limestone pavement and sand
dunes. In a comprehensive study of the vegetation of Anegada, V.
rupicola was found in higher abundance (based on percentage occurrence
across plots) on limestone but also widespread within the sand dunes
(Clubbe et al. 2004, p. 344). Occurrence of the species on sand dunes
on Anegada may explain the new record of the species in the northern
coast (Tortuguero Lagoon) of Puerto Rico within an area that is
characterized by the presence of white sands soils (O. Monsegur,
Service, pers. obs., 2013).
Life History
Agave eggersiana
Based on the information currently available to us, there is no
published information describing the ecology and genetics of Agave
eggersiana. Although samples from individuals in the Gallows Bay area
have been collected for genetic analysis (Ray, VFR, pers. comm., 2010),
the Service is unaware if the samples were analyzed and results have
been published. No further information is available regarding the
ecology of the species beyond the demographic trends discussed above.
Gonocalyx concolor
Gonocalyx concolor has been observed flowering in December,
January, February, and April (Nevling 1970, p. 224). Preliminary
studies of the species' reproductive biology indicate that the plant is
predominantly outcrossed, and that outcrossed flowers produce twice the
number of seeds than self-pollinated flowers (S. Flores, Universidad
del Turabo, pers. comm. 1996). The low number of individuals per
population may suggest that Gonocalyx concolor has highly specialized
ecological requirements to grow and that production of viable seeds
rarely occurs (C. Pacheco, Service, pers. obs., 2013). Although a
number of authors have reported the species on flower and fruit, no one
has observed recruitment. Currently, no information about reproductive
capacity, dispersion, or habitat requirements is available for G.
concolor.
Varronia rupicola
Studies on the distribution, abundance, and reproductive biology of
Varronia rupicola have been conducted by scientists from the University
of Puerto Rico, Mayag[uuml]ez Campus (Breckon and Kolterman 1996, p. 6;
Monsegur and Breckon 2007, p. 13). These authors reported the species
flowering and fruiting in December through January (Breckon and
Kolterman 1996, p. 4), and in June through July (Monsegur and Breckon
2007, p. 1). From February to April, all plants observed were sterile.
Fruit production in the populations from the Gu[aacute]nica
Commonwealth Forest and the municipality of Ponce seem to be high, and
there is evidence of recruitment associated to the majority of the
clusters of individuals (O. Monsegur, Service, pers. obs., 2013). Under
greenhouse conditions, seed germination has been reported as not less
than 67 percent (Wenger et al. 2010). Germination in the wild has also
been observed to be high (O. Monsegur, Service, pers. obs., 2013).
However, apparently there is also a high mortality of seedlings, and
only few individuals make the transition (natural thinning) to sapling
stages (O. Monsegur, Service, pers. obs., 2013). Monsegur and Breckon
(2007, p. 2) reported numerous seedlings (>140) and various saplings in
the Gu[aacute]nica Commonwealth Forest. However, seedling recruitment
on Vieques Island seems to be low, as it has not been recorded during
recent assessments (Monsegur and Breckon 2007, p. 7; Hamilton, KEW,
pers. comm., 2013). Despite the showy red fruits of Varronia rupicola,
its dispersion seems to be almost limited by gravity, as the majority
of the seedlings lie under the parent tree or downslope (O. Monsegur,
Service, pers. obs. 2013). The wide range of the species suggests a
former animal disperser (probably a bird). Patterns of plant-animal
interactions were probably altered due to the previous extensive
deforestation of the island of Puerto Rico. Some observations of seed
dispersal by an undetermined vector have been reported from Anegada
(Hamilton, KEW, pers. comm., 2013). If not extinct, possible dispersers
may have altered their foraging behavior and now do not feed on the
fruits of V. rupicola. Recent observations in Puerto Rico indicate that
flowers of V. rupicola are visited by several insect species, including
Apis mellifera (honey bee) and Electrostrymon angelia (fulvous
hairstreak, a butterfly) (O. Monsegur, Service, pers. obs. 2013).
Varronia rupicola material germinated in the greenhouse at Cabo
Rojo National Wildlife Refuge in Cabo Rojo were flowering and producing
fruits in about 1 year after germination (O. Monsegur, Service, pers.
obs., 2013). The rapid reproductive development of the species and the
finding of individuals along recently disturbed sites (new dirt roads)
and natural forest gaps (openings) may indicate that V. rupicola is an
early colonizer or pioneer species.
Historical Range
Agave eggersiana
Historically, Agave eggersiana was reported from the north coast in
Christiansted, St. Croix, and along the south coast of the island
(Proctor and Acevedo-Rodr[iacute]guez 2005, p. 118). Britton and Wilson
(1923, p. 156) reported the species from hillsides and plains in the
eastern dry districts of St. Croix, but did not provide population
estimates. In addition, it was reported that A. eggersiana was
cultivated on St. Croix and St. Thomas for ornament (Trelease 1913, p.
28; Britton and Wilson 1923, p. 156; Proctor and Acevedo-
Rodr[iacute]guez 2005, p. 118). Information provided (Kojis and Boulon,
DPNR, pers. comm., 1996) specified that the species was last observed
growing in the wild around 1984 to 1986 on St. Croix. In 2003, DPNR
stated that the species was believed to be extinct (Plaskett, DPNR,
pers. comm. 2003; Dalmida-Smith, DPNR, pers. comm., 2010). Proctor and
Acevedo-Rodr[iacute]guez (2005, p. 118) provided a general description
of A. eggersiana and state that the species appeared to be extinct in
the wild.
[[Page 62565]]
However, no citations or survey information were provided to support
this statement. Subsequently, in 2010, DPNR provided information based
on field visits and reported the existence of several populations of A.
eggersiana on St. Croix (Dalmida-Smith, DPNR, pers. comm., 2010).
Historically, land use intensity increased by colonial exploitation
since the 15th century (Chakroff 2010, p. 6). Sugarcane was the main
crop on the island and dominated the economy for nearly 200 years (Shaw
1933, p. 414). Apparently, the former land use of the areas used for
sugar cane cultivation resulted in degradation of the species' habitat
and nearly extirpated the species from the wild. Sugarcane is no longer
cultivated commercially on the island, the majority of the areas
formerly used for sugarcane plantations are currently grasslands, and
early secondary forests are dominated by the nonnative tree Leucaena
leucocephala (white leadtree).
Gonocalyx concolor
Gonocalyx concolor was first discovered on Cerro La Santa at an
elevation of approximately 2,962 ft (903 m) in the Carite Commonwealth
Forest, east-central Puerto Rico (Nevling 1970, p. 221). In 1993, Dr.
Frank Axelrod found a second population of this species close to the
Charco Azul recreational area, also in the Carite Commonwealth Forest
(Axelrod 1993, UPR herbarium voucher 6643). This population is located
at an approximate elevation of 2,070 ft (630 m) in the ausubo forest,
which lies within the basin of the R[iacute]o Grande de Patillas,
approximately 2 mi (3.2 km) southeast from Cerro La Santa. Later, in
December 2006, Omar Monsegur (former student from the University of
Puerto Rico) visited the known localities describing three populations
of Gonocalyx concolor in the Carite Commonwealth Forest: two at Cerro
La Santa, and another at Charco Azul (O. Monsegur, UPRM, unpubl.
report, 2006, p.1). Dr. Samuel Flores (pers. comm., 1996), professor at
the Turabo University in Puerto Rico, anecdotally reported the species
from El Yunque National Forest in the Luquillo Mountains, northeastern
Puerto Rico. Despite of Service efforts to locate the species in El
Yunque National Forest, it has not been found. Therefore, this record
has not been confirmed.
Varronia rupicola
Varronia rupicola was first discovered by the German botanical
collector Paul Sintenis in July 1886, in the Los Indios Ward, located
between the Barinas ward in Yauco and the municipality of Guayanilla,
Puerto Rico. It was later found in Gu[aacute]nica, Puerto Rico, in
1887, and again in 1943 and 1959 (Proctor 1991, p. 66). The species was
thought to be endemic to Puerto Rico, until it was collected by George
Proctor in May 1987, at the west end of the island of Anegada, British
Virgin Islands (Proctor 1991, p. 66). Proctor (1994, p. 54) also
reported a specimen from Punta J[aacute]lova on Vieques Island, Puerto
Rico. This report was based on a specimen collected by Woodbury,
possibly around 1978. Surveys conducted by Breckon and Kolterman in
1995 located the species at a site called El Pe[ntilde][oacute]n in the
municipality of Pe[ntilde]uelas (Breckon and Kolterman 1996, p. 6). In
2003, three individuals of V. rupicola were found adjacent to the
entrance of El Fuerte Trail within the Gu[aacute]nica Commonwealth
Forest (M. Canals, DNER, pers. comm., 2004). In 2005, an individual of
V. rupicola was found on Lighthouse Peninsula, Vieques Island (Breckon
and Kolterman 2005, p. 1). This area is located within the Vieques
Island National Wildlife Refuge.
Current Range
Agave eggersiana
Agave eggersiana is currently found on the north and south coasts
of St. Croix, USVI. Seven populations support approximately 313 adult
plants and more than 316 juveniles. It is uncertain if these
populations are natural (individuals that come from wild populations)
or if these populations consist of individuals that escaped from
landscaping. However, characteristics, such as growing mixed with
native vegetation, evidence of natural recruitment, and the presence of
different size classes, suggest these are remnants of wild populations.
The current distribution of populations of Agave eggersiana on St.
Croix that are presumed to be wild is as follows:
a. North coast--(1) Gallows Bay with an estimate of 2 individuals;
and (2) Protestant Cay with an estimated 40 individuals.
b. South coast--(3) Manchenil Bay with an estimated 8 individuals;
(4) West side of Vagthus point with a single individual; (5) Great Pond
with approximately 65 individuals; (6) South Shore with an estimate of
182 individuals; and (7) Cane Garden Bay with 15 individuals.
Most of the sites have juvenile individuals except for Gallows Bay
and Vagthus Point (Table 1).
Table 1--(Presumed) Wild Populations of Agave eggersiana
----------------------------------------------------------------------------------------------------------------
Number of individuals
Population Area/ location Estate Ownership (adults/juveniles)
----------------------------------------------------------------------------------------------------------------
South Shore................... South Coast...... Cane Garden...... Private.......... 182/231
Cane Garden Bay............... South Coast...... Cane Garden...... Private.......... 15/27
Manchenil Bay................. South Coast...... Granard.......... Private.......... 8/58
Protestant Cay................ North Coast...... Protestant Cay... Government but 40/Undetermined
leased to
private party.
Gallows Bay................... North Coast...... Mount Welcome.... Private.......... 2/0
West Vagthus Point............ South Coast...... Peters Minde..... Private.......... 1/0
Great Pond.................... South Coast...... Great Pond....... Government....... 65/Undetermined
------------------------
Total..................... ................. ................. ................. 313/316+
----------------------------------------------------------------------------------------------------------------
Sources: O. Monsegur and M. Vargas, Service, unpubl. data, 2010 and 2013; Dalmida- Smith, DPNR, pers. comm.,
2010; David Hamada, SGVBG, pers. comm., 2010; Plaskett, DPNR, pers. comm., 2003.
In addition, there are introduced individuals located at Salt River
National Park and Ecological Preserve (SARI) with an estimate of 90
individuals (mostly juveniles); Buck Island National Monument with an
estimate of 11 individuals; and Ruth Island with 1 individual (O.
Monsegur and M. Vargas, Service, pers. obs., 2010 and 2013; Dalmita-
Smith, DPNR, pers. comm., 2010).
[[Page 62566]]
Gonocalyx concolor
Currently, Gonocalyx concolor is known from three populations: two
at Cerro La Santa and another at Charco Azul, both in the Carite
Commonwealth Forest (Pacheco and Monsegur, Service, unpubl. report,
2013, p. 2). The species shows a limited distribution in its habitat,
occupying only 0.75 ac (0.3 ha) at Cerro La Santa (Pacheco and Monsegur
Service, unpubl. report, 2013, p. 3) and approximately 0.12 ac (0.05
ha) at Charco Azul (O. Monsegur, UPRM, unpubl. report, 2006, p.2). The
individuals reported from El Yunque National Forest are apparently no
longer extant. According to Luis Rivera, Tropical Vegetation
Specialist, the U.S. Forest Service does not have records of the
species in El Yunque National Forest (L. Rivera, USFS, pers. comm.,
2013). Despite the availability of habitat, the Service considers that
the report from El Yunque National Forest may be a misidentification of
material from G. portoricensis.
In 1992, Dr. George R. Proctor conducted a status review of the
species estimating its population at Cerro La Santa at around 35
individuals (Proctor 1992, p. 4). Later, Dr. Samuel Flores (professor
from the Turabo University) visited the same area and estimated its
population at around 172 individuals (S. Flores, pers. comm., 2009). In
December 2006, Omar Monsegur (graduate student from the University of
Puerto Rico, Mayag[uuml]ez Campus) estimated approximately 25
individuals at Cerro La Santa and 4 individuals at Charco Azul (O.
Monsegur, UPRM, unpubl. report, 2006, p. 1). In 2013, Service
biologists, Carlos Pacheco and Omar Monsegur, visited the population at
Cerro La Santa and estimated the G. concolor population at around 27
individuals (Pacheco and Monsegur, USFWS, unpubl. report, 2013, p. 3).
Varronia rupicola
Varronia rupicola is currently known from at least seven main
localities in Puerto Rico (Table 2) and several localities from the
island of Anegada. Monsegur and Breckon (2007, p. 1) visited the
historical localities in Puerto Rico and provided updated information
about the status and distribution of the species. The distribution of
V. rupicola in the Gu[aacute]nica Commonwealth Forest extents to at
least six small populations or subpopulations within the east section
of the forest. Another population was located on the west unit of the
Gu[aacute]nica Commonwealth Forest by Alcides Morales (Sociedad
Ornitologica Puertorique[ntilde]a, Inc., pers. comm., 2012). This is
the westernmost recorded distribution for the species.
From the municipality of Pe[ntilde]uelas, Monsegur and Breckon
(2007, p. 6) found a single individual in a ravine area on the west
side of El Pe[ntilde][oacute]n site. This seems to be part of the same
population identified by Breckon and Kolterman in 1995. In addition,
the Service confirmed the presence of about eight clusters of the
species in an area just north of the Ponce Holiday Inn in the
municipality of Ponce (O. Monsegur, Service, and J. Sustache, DNER,
unpubl. Data, 2013).
Table 2--Status of Currently Known Populations of Varronia rupicola
----------------------------------------------------------------------------------------------------------------
Number of
Localities reproductive Number of Number of Total of
individuals saplings seedlings plants
----------------------------------------------------------------------------------------------------------------
El Pe[ntilde][oacute]n (Pe[ntilde]uelas)........ 16 0 0 16
Gu[aacute]nica Commonwealth Forest (East)....... 34 30 142 206
Gu[aacute]nica Commonwealth Forest (West) 1 0 0 1
(Montalva).....................................
Puerto Ferro (Vieques NWR)...................... 6 0 0 6
Yauco (Montes de Barina)........................ 2 0 0 2
Ponce (Holiday Inn)............................. 17 4 120 141
Tortuguero Lagoon (DNER)........................ 1 0 0 1
---------------------------------------------------------------
Total....................................... 77 34 262 373
----------------------------------------------------------------------------------------------------------------
Another recorded site for Varronia rupicola lies within a privately
owned property located at Montes de Barinas in the municipality of
Yauco (C. Pacheco, Service, pers. comm., 2011). The species was also
reported by Alcides Morales (Sociedad Ornitologica
Puertorique[ntilde]a, Inc., pers. comm., 2012) from a nearby property
known as Finca Catal[aacute]. This property is adjacent to the locality
reported by Pacheco on 2011. These reports overlap with the general
area where this specimen was collected by Paul Sintenis in 1886.
There is new information suggesting the existence of one population
within the Tortuguero Lagoon in northern Puerto Rico (Beverly Yoshioka,
Service, pers. comm., 2013). This will be the first record for the
species in the northern coast of Puerto Rico. The finding of this new
locality is supported by the existence of the species on a similar
habitat in the Island of Anegada (British Virgin Islands). Varronia
rupicola is also found in the northwest section of Anegada, where it is
reported as common (Clubbe et al., 2004, p. 344; McGowan et al., 2006,
p. 5).
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1533), and its implementing
regulations at 50 CFR part 424, set forth the procedures for adding
species to the Federal Lists of Endangered and Threatened Wildlife and
Plants. Under section 4(a)(1) of the Act, we may list a species based
on any of the following five factors: (A) The present or threatened
destruction, modification, or curtailment of its habitat or range; (B)
overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; and (E) other natural or manmade
factors affecting its continued existence. Listing actions may be
warranted based on any of the above threat factors, singly or in
combination. Each of these factors is discussed below.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
Agave eggersiana
The Agave eggersiana population found in Great Pond is the only one
located in a conservation area. The remaining populations occur within
privately owned lands and are threatened by development, or are growing
in areas that are already developed and managed as tourism and
residential projects and that will not support the continued existence
of the plants. Based on information reported by the University of the
Virgin Islands'
[[Page 62567]]
Conservation Data Center (USVI-CLWUP 2004), at least three of the
populations (i.e., Protestant Cay, Gallows Bay, and Manchenil Bay) lie
within areas identified by DPNR as high-density land use areas, and
thus have a higher susceptibility to development in the near future.
The coastal areas that harbor suitable habitat for the species are
currently subject to urban and tourist development (O. Monsegur and M.
Vargas, Service, pers. obs., 2010 and 2013). At least two proposed
development projects have been identified within suitable habitat for
the species (i.e., C&R Robin, LLC, and Seven Hills Beach Resort and
Casino) (Weiss, CBD, pers. comm., 2010). Current information regarding
the status of these development projects is not available to the
Service.
The population at Protestant Cay has been affected by construction
and management activities associated with the current use of the area,
i.e., the disposal of garden debris from a hotel in the species' known
habitat (O. Monsegur and M. Vargas, Service, pers. obs., 2010). As
Agave eggersiana relies on asexual reproduction, the species depends on
the bulbils becoming established. Covering the bulbils with debris may
result in subsequent mortality of the bulbils and lack of natural
recruitment, thus affecting the long-term survival of this population.
Moreover, individuals located on the edges of the population are pruned
as part of the gardens' maintenance. This practice may result in
mortality or mutilation of individuals because the species is
monopodial (single growth axis). The population at Protestant Cay is
also threatened by competition with nonnative plant species. In this
case, habitat modifications from urban development (e.g., road) and
garden maintenance have created conditions for the establishment of
invasive, nonnative species. Also, the undeveloped habitat on the cay
is being rapidly colonized by nonnative species (see Factor E
discussion, below). A. eggersiana plants also seem to be stressed by
competition with nonnative plants.
Another modification of habitat in the area was a sand ramp
constructed in 2011, on the northeast side of the cay (T. Cummins and
W. Coles, DPNR, pers comm., 2011; R. Platenberg and T. Cummins, DPNR,
pers. comm., 2012; Zegarra, Service, pers. comm., 2012). It was
documented that at least five individuals of Agave eggersiana were
crushed or otherwise impacted by the excavation work (R. Platenberg and
T. Cummins, DPNR, pers. comm., 2012).
The individuals located at Gallows Bay are within a developed
residential complex that has the potential for future expansion, and
thus may affect Agave eggersiana (O. Monsegur and M. Vargas, Service,
pers. obs., 2010 and 2013). Moreover, the Gallows Bay area does not
contain additional habitat to allow for population expansion. Remaining
forested areas surrounding this location are characterized by an
abundance of nonnative species. The small pockets that could be
colonized by bulbils are occupied by Sansevieria cylindrica (African
spear), a nonnative plant species that tends to form a complete cover
of the understory (see Factor E discussion, below).
The area from Cane Garden Bay to Manchenil Bay on the south coast
of St. Croix harbors four of the known natural populations of Agave
eggersiana (Manchenil Bay, Vagthus Point, Cane Garden, and South
Shore). According to DPNR personnel (Valiulis, pers. comm., 2010),
these areas are advertised by realtors for tourism and residential
development. Furthermore, the areas along the south coast that have not
been developed are used for cattle or hay production, minimizing the
recovery of native vegetation and, therefore, the habitat for A.
eggersiana (O. Monsegur and M. Vargas, Service, pers. obs., 2010 and
2013). The development of tourist and residential projects in these
coastal areas may result in the extirpation of some populations or, at
the least, will reduce the chances of the populations to expand or to
colonize other areas. The effects of development projects are
exacerbated by the low potential for natural recruitment due to the
small number of populations and individuals.
The population of Great Pond is located between the entrance road
of the East End Marine Park office and a private property currently
advertised for sale. The population seems to be healthy based on the
presence of different size plants and evidence of recent flowering
events. However, the area near the population is mowed, and the access
road limits the expansion of the population. Furthermore, the property
adjacent to the population is privately owned and currently for sale
(O. Monsegur and M. Vargas, Service, pers. obs., 2010 and 2013). The
possible use of the area for additional residential or tourist
development may affect the Agave eggersiana population. Owners will
likely manage their properties as landscapes, which could lead to land
clearing, additional mowing, other maintenance activities, and the
introduction of nonnative plants. Moreover, the abundance of grasslands
and the dominance of the nonnative plant Megathyrsus maximus (guinea
grass) make the population of A. eggersiana susceptible to human-
induced fires (addressed under Factor E, below).
Gonocalyx concolor
Habitat destruction and modification have been identified by
species expert as the main threat to Gonocalyx concolor (Proctor 1992,
p. 3; O. Monsegur, UPRM, unpubl. data, 2006; C. Pacheco and O.
Monsegur, Service, unpubl. report, 2013, p. 3). In 1974, the
Commonwealth of Puerto Rico granted special use permits for the
construction of telecommunications facilities, and governmental and
recreational facilities, within G. concolor habitat, affecting
approximately 107 ac (43.5 ha) of lower montane very wet forest
(Silander et al. 1986, p. 178). Currently known populations of G.
concolor at Cerro La Santa are found in remnants of elfin forest
vegetation located adjacent (less than 246 ft (75 m)) from
telecommunication facilities, and at the edges (less than 9.8 ft (3 m))
of the road that provide access to the telecommunication facilities (C.
Pacheco and O. Monsegur, Service, unpubl. report, 2013, p. 3). Below we
discuss the three factors that may affect the current habitat or range
of G. concolor: (1) Installation of telecommunication towers; (2) road
improvement; and (3) vegetation management.
Land-use history of Cerro La Santa has shown that installation of
telecommunication facilities for television, radio, and cellular
communication, and for military and governmental purposes, has
adversely impacted Gonocalyx concolor habitat (Silander et al., 1986,
p. 178), and although not documented, presumably has directly affected
individuals of the species. George Proctor (1992, p. 3) stated that the
construction of a paved road and gigantic telecommunication towers on
the summit ridge of Cerro La Santa destroyed much of the natural
population of this species. Currently, the telecommunication tower and
its associated facilities (i.e., access roads, security fences, guy
wires) occupy approximately 6.1 ac (2.5 ha) of the elfin forest in
Cerro La Santa; this is habitat that the species may have occupied in
the past (C. Pacheco and O. Monsegur, Service, unpubl. report, 2013, p.
3). Although the populations at Cerro La Santa are located within a
Commonwealth forest, this area is subjected to development for
expansion of telecommunication infrastructure because permits to build
new communication facilities or expand currently existing ones within
or near Commonwealth forests are prevalent
[[Page 62568]]
(DNER 2004a, p. 2). Expansion of the existing telecommunication
facilities may result in loss of 27 individuals of G. concolor and
their habitat. In Puerto Rico, towers for cellular communication,
radio, television, and military and governmental purposes have
represented a threat to those plant species that happen to occur only
on mountaintops. The proliferation of these antennas has increased with
the advent of cellular phone and related technologies. While the towers
themselves may not occupy a very large area, construction activities,
access roads, and other facilities have a much wider impact, resulting
in the elimination of potential habitat for the species.
For the above reasons, we determined that installation of
additional communications towers or expansion of the existing one at
Cerro La Santa is a threat to Gonocalyx concolor by direct mortality
and due to permanent loss, fragmentation, or alteration of its habitat.
Construction of a new access road and improvement of the existing
access road to the existing communication facilities have been
identified as a factor that could directly (destruction of individuals)
or indirectly (slope instability and habitat degradation) reduce the
number Gonocalyx concolor and its habitat at Cerro La Santa (Proctor
1992, p. 3; C. Pacheco and O. Monsegur, Service, unpubl. report, 2013,
p. 3). Further, expanding the road that provides access to the
telecommunication facilities may negatively affect the species' habitat
and could result in loss of 11 mature individuals of G. concolor (C.
Pacheco and O. Monsegur, Service, unpubl. report, 2013, p. 3).
Additionally, clearing the native vegetation along the road may
facilitate and accelerate colonization of invasive vegetation towards
G. concolor habitat (see Factor E discussion, below). Destruction or
modification of this kind of habitat may be irreversible. Therefore,
the microhabitat conditions necessary for the recovery of the species
may be lost if the habitat is modified for the expansion of the
existing telecommunications facilities or construction of new
communication facilities.
Vegetation management around the existing telecommunication towers
and associated facilities and along the existing power lines that
energize these facilities is a threat to Gonocalyx concolor and its
habitat (C. Pacheco and O. Monsegur, Service, unpubl. report, 2013, p.
3). Telecommunication companies periodically remove vegetation along
the access roads, around the security fences, and under the guy wires
(tensors) that are anchored in the forest. Additionally, maintenance
staff of the Puerto Rico Energy and Power Authority (PREPA)
periodically trim and clear the vegetation under the existing power
lines that provide energy to the telecommunication facilities and
adjacent communities. Presently, the Puerto Rico Department of Natural
and Environmental Resources (DNER) is aware of the presence of G.
concolor and the need to implement conservation measures for the
species in Cerro La Santa. The existing telecommunication facilities
and PREPA usually have a restricted perimeter delimiting the area that
can be mowed and trimmed. However, maintenance activities outside of
the perimeter have been conducted without the coordination with the
forest manager, affecting the forest vegetation and G. concolor habitat
(Hecsor Serrano-Delgado, DNER, pers. comm., 2013; O. Monsegur, UPRM,
unpubl. report, 2006, p.1). In 2006, Omar Monsegur documented damages
to an individual of G. concolor caused by vegetation removal activities
outside of the fences (O. Monsegur, UPRM, unpubl. report, 2006, p.1).
Additionally, clearing the native vegetation along the access roads,
around the telecommunication facilities, and under the power lines may
facilitate and accelerate colonization of invasive vegetation in G.
concolor habitat. See Factor E, below, for further discussion on
invasive species.
Even though the population dynamics of the species are poorly
known, we understand that the impacts discussed above could be
detrimental to the species as a whole. Clearing of vegetation may
result in direct impacts (cutting of individuals) or indirect impacts
(by opening forest gaps that can serve as corridors for invasive
species) to the species. Vegetation management and maintenance of
communication towers and facilities are a threat to Gonocalyx concolor
due to changes in microclimate (a local atmospheric zone where the
climate differs from the surrounding area) and plant species
composition. Also, vegetation management around the existing facilities
and along the access roads may be a direct and indirect threat to the
G. concolor because it may alter the habitat condition, allowing
invasive plants to colonize the area, and may result in direct physical
damage to the species.
Varronia rupicola
The species' rarity and restricted distribution make it vulnerable
to habitat destruction and modification. About 50 percent of known
Varronia rupicola individuals in Puerto Rico occur on private lands
(i.e., Yauco, Pe[ntilde]uelas, and Ponce) in areas subject to urban
development. Moreover, the habitat at Pe[ntilde]uelas and Ponce may
remain underestimated in relation to the presence of the species as the
area has not been extensively explored. The habitat in the
municipalities of Pe[ntilde]uelas and Ponce has been severely
fragmented for urban development (i.e., housing projects, hotels,
jails, landfills, rock quarries, and Puerto Rico Highway Number 2 (PR
2)). The habitat has been further fragmented by the use of these
forested areas by PREPA as a right-of-way for power lines, and
additional habitat was impacted for a former proposed gas pipeline
(Gasoducto Sur). At least 1,200 ac (485 ha) of prime dry forest habitat
from Gu[aacute]nica to Ponce are currently proposed for urban and
industrial developments, which are evaluated by the Puerto Rico
planning board (https://www.jp.gobierno.pr). These include the areas
where the Ponce populations were recently located by Service staff.
Future projects may threaten these populations with fragmentation, and
possibly extirpate currently known individuals. Despite the species'
biology suggesting its ability to colonize disturbed areas, it is very
likely that once the habitat is fragmented. V. rupicola will be
outcompeted by nonnative plant species (see Factor E discussion).
In Pe[ntilde]uelas, the species is found in an area that is
currently under urban development. Breckon and Kolterman (1996)
reported a healthy population of Varronia rupicola in this area located
at El Pe[ntilde][oacute]n de Ponce (Municipality of Pe[ntilde]uelas),
which is part of a residential development called ``Urbanizaci[oacute]n
El Pe[ntilde][oacute]n.'' At this site, V. rupicola plants grows within
residential lots, and although the lots are large in size, current and
ongoing construction and deforestation (some lots have been completely
cleared for house construction) threaten this population. In 2007,
Monsegur and Breckon (2007, p. 6) reported that one individual plant
adjacent to ``Urbanizaci[oacute]n El Pe[ntilde]on'' was eliminated by
the improvement of PR 2. The authors reported that vegetation was
removed and the area was bulldozed, apparently as part of a project to
control run-off from the ravine.
In Yauco, the species occurs within private properties that may be
subject to urban development (https://www.jp.gobierno.pr). In fact,
urban development has encroached remnants of native dry forest areas,
resulting in the isolation or disjunction of populations of rare
plants, hence,
[[Page 62569]]
reducing suitable habitat for the species. These areas are also
threatened by deforestation for agricultural practices such as raising
cattle, cattle grazing, and for the extraction of fence posts (O.
Monsegur, Service, pers. obs., 2005). The known population at Yauco was
observed at the edge of an existing dirt road. Therefore, any road
expansion may result in the extirpation of individuals, habitat
modification, and intrusion of nonnative plants.
In the Gu[aacute]nica Commonwealth Forest and the Vieques Island
National Wildlife Refuge (NWR), Varronia rupicola is found at the edge
of trails and roads, making the species prone to be affected by
management activities (e.g., widening of trails, road repairs).
Additionally, several individuals of V. rupicola are found underneath
power lines of PREPA at the Gu[aacute]nica Commonwealth Forest, where
they are threatened by maintenance activities such as cutting or the
use of herbicides. PREPA has the right to access the power lines for
maintenance and service in case of emergencies. Damage to individual
plants caused by maintenance activities has been observed in the past
(O. Monsegur, Service, pers. obs., 2009). This makes a significant part
of the Gu[aacute]nica populations prone to extirpation despite the
existence of regulatory mechanisms (see Factor D discussion, below).
Furthermore, despite being a National Wildlife Refuge, the Vieques
site (Puerto Ferro) is considered as an active ammunition site due to
the previous use of Vieques Island as a bombing range by the U.S. Navy
(https://public.lantops-ir.org/sites/public/vieques/default.aspx).
Although there are no current plans to conduct vegetation removal to
investigate the ammunitions in Puerto Ferro (F. Lopez, Service, pers.
comm., 2013), the investigation process at Vieques has proved to be
dynamic and there is a possibility that clearing of native vegetation
will be required to conduct removal of ammunitions in the future.
Varronia rupicola is also found in the western half of Anegada
Island, and the population appears to be healthy. However, despite
efforts to maintain biodiversity and promote conservation on Anegada,
V. rupicola, along with other rare plant species and their preferred
limestone habitat, faces threats of future habitat fragmentation,
habitat modification, and invasive species (Pollard and Clubbe 2003, p.
5; McGowan et al., 2006, p. 4). Anegada is under heavy pressure for
residential and tourism development (McGowan et al., 2006, p. 4),
resulting in improvement and construction of roads, which increase
habitat loss and fragmentation.
About half of known populations and suitable habitat are within
privately owned land, which is being modified or proposed to be
modified for urban development. These activities are expected to
continue.
Conservation Efforts To Reduce the Present or Threatened Destruction,
Modification, or Curtailment of Its Habitat or Range
Agave eggersiana
Efforts to re-establish locally endangered plant species to the
wild are occurring within properties managed by the National Park
Service (NPS) (SARI and Buck Island Reef National Monument) on St.
Croix. The intent of NPS is to increase production of the species'
progeny around the island, which started in 2007, by planting seven
individuals of Agave eggersiana (NPS, unpubl. data, 2007). Also, an
intra-agency agreement between the Service and NPS, in cooperation with
the Florida and Caribbean Exotic Plant Management Team, was established
in 2007, to control nonnative, invasive plants and restore coastal
landscape. The agreement was to restore approximately 15 acres (6.1 ha)
of SARI coastal wetlands and uplands. The agreement also included
planting A. eggersiana among other native flora. Currently, there are
more than 100 juvenile plants on NPS lands. However, there is the need
to continue monitoring these plants to document their long-term
survival and recruitment, and to adaptively manage the population.
Other efforts include the evaluation of the status of the natural
populations by Service staff. In 2010 and 2013, Service biologists
visited St. Croix and found Agave eggersiana planted at the Lagoon
Picnic Area, a public beach that seems to be under a reforestation
effort funded by the Antilitter and Beautification Commission. The site
harbors about 220 plants that are part of the landscape. Although the
Service has no information on the reforestation project, it seems to be
a good effort for the protection of coastal habitat and as an outreach
effort towards the protection of the species.
Gonocalyx concolor
Gonocalyx concolor populations occur on public lands managed for
conservation by the Puerto Rico DNER. The DNER develop a management
plan for all Commonwealth Forests in 1976; however, specific measures
to protect this species are not included in the plan (DNR 1976, pp.
168-181). Currently, activities to be conducted within Commonwealth
Forest are generally scrutinized, and measures to minimize or avoid
impacts to species protected by DNER and Federal agencies are
recommended and implemented (see Factor D discussion). However,
authorized activities, such as vegetation clearing around communication
towers, under power lines, and along roads,have been documented,
resulting in loss of individuals and the species' habitat.
Varronia rupicola
The Service's Caribbean Ecological Service Field Office (CESFO) has
evaluated federally funded projects or federally related projects
requiring federal permits that lie within the species' range. As part
of the evaluation, the Service recommends surveys to identify
populations and recommends conservation measures to protect the
species. However, residential projects without Federal nexuses are not
submitted to the Service for evaluation.
Summary of Factor A
Agave eggersiana
The threats of possible construction and developments, and the
current management of the habitat of the populations, may further limit
the species. Direct consequences can be expected as impacting (harming)
the individuals (e.g., cutting or mowing), while indirect consequences
can be expected to create a habitat disturbance where nonnative plants
can overpower Agave eggersiana. Currently, there continue to be impacts
on various populations that are expected to continue into the future.
Gonocalyx concolor
The species' rarity and restricted distribution makes it vulnerable
to habitat destruction and modification. The scope of these factors is
exacerbated because the most significant portion of the known
population occurs adjacent to telecommunication facilities and at the
edge of the existing access road. The activities related to these
facilities are expected to continue into the future. Therefore, they
are likely to have significant impact on Gonocalyx concolor.
Varronia rupicola
Degradation of habitat represents a threat to Varronia rupicola.
About half of the known populations of V. rupicola and its suitable
habitat are within privately owned land, which is being modified or is
proposed to be modified for urban development. In addition, habitat
fragmentation by clearing of vegetation, road constructions, and
[[Page 62570]]
right-of-way maintenance (cutting plants and used of herbicides) can
limit the species' survivability where these activities create the
conditions for nonnative plants to outcompete V. rupicola. We expect
that this threat would continue into the future.
Factor B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Agave eggersiana
Agave eggersiana has been reported as a cultivar since it was
described as a species in 1913 (Trelease 1913, p. 28). Historically,
the majority of A. eggersiana found on St. Croix and St. Thomas were
from landscaped areas (Britton and Wilson 1923, p. 156; Plaskett, DPNR,
pers. comm., 2003; Kojis and Boulon, DPNR, pers. comm., 1996; Proctor
and Acevedo-Rodr[iacute]guez 2005, p. 118; Acevedo-Rodr[iacute]guez,
pers. comm., 2005). Currently, the species is distributed by the St.
George Botanical Garden and the St. Croix Environmental Association for
conservation and private landscaping purposes. In fact, it is an
ornamental species commonly used on the island of St. Croix. Recent
declines in the number of individuals at one population along the coast
of Manchenil Bay are thought to be due to collection for ornamental
purposes (Dalmida-Smith, DPNR, pers. comm., 2010; Valiulis, DPNR, pers.
comm., 2010). At present, we do not have evidence to confirm this
threat. However, when Service biologists visited the island in 2010 and
2013, they observed that A. eggersiana continues to be used as a
landscape species.
Current evidence suggests that the wild and cultivated populations
of Agave eggersiana have minimum genetic variation. Data suggest that
cultivated individuals could be used as genetic stock to aid in the
long-term survival of this species. However, most cultivated
populations are groomed and do not allow natural recruitment.
Therefore, we are concerned about possible collection of individuals
from natural populations for landscaping. The rarity and low numbers of
individuals for this agave may result in a high ornamental value. The
limited reproduction of the plant, which reproduces only once every 10
to 15 years (D. Hamada, SGVBG, pers. comm., 2010), may lead people to
collect individuals from the wild and thus lower the recruitment of
those limited populations and risk the continued survival of the
species.
Gonocalyx concolor
Gonocalyx concolor is not a commercially valuable species or a
species sought after for recreational or educational purposes. However,
the species is recognized by its rarity and restricted range, making it
more attractive to collectors and scientists. Collection could be a
significant threat to the species due to the few remaining populations,
small population size, restricted range, remoteness of occupied
habitat, and the potential for collection to occur at any time. Because
little is known about G. concolor (i.e., abundance, distribution,
habitat requirement, and phenology), any collection of seedlings,
saplings, flowers, fruits, or parts of the individual without
appropriated evaluation of its effect on the species could adversely
affect the status of the population. Even limited collection from the
remaining population could have deleterious effects on reproductive and
genetic viability of the species and could contribute to its extinction
(Jos[eacute] Sustache, DNER, pers. comm., 2013). Although we consider
collection to be a potential threat to this species, we do not have
information indicating that the species is being collected for
commercial, recreational, scientific or educational purposes.
Varronia rupicola
There is scientific interest in Varronia rupicola from local and
external botanists. In fact, there is ongoing research by personnel
from the Royal Botanic Gardens (KEW) related to the reproductive
biology, propagation, and genetics of this species, including the
populations from United States and British territories (entire Puerto
Rican platform). However, the current available information on the
species does not suggest that overutilization for commercial,
recreational, scientific, or educational purposes has contributed to a
decline of V. rupicola. This research is the only known use of the
species, and it is strictly for scientific purposes. Therefore, despite
its rarity, we do not have any evidence that suggests this threat is
negatively impacting V. rupicola.
Conservation Efforts To Reduce Overutilization for Commercial,
Recreational, Scientific, or Educational Purposes
Agave eggersiana
At present, the Service is unaware of any conservation efforts to
reduce overutilization for commercial, recreational, scientific, or
educational purposes of Agave eggersiana, except for the existing
regulatory mechanisms that protect the species. However, although A.
eggersiana is protected by Act No. 5665, the USVI law that provides
protection to indigenous, endangered, and threatened fish, wildlife,
and plants in the Territory, the use of the species for landscaping
continues to be a practice. This law prohibits the collection of
endangered species. However, we do not have information about
enforcement mechanisms to avoid the use of this plant for landscaping
(see Factor D discussion, below).
Gonocalyx concolor and Varronia rupicola
The Carite and Gu[aacute]nica Commonwealth Forests are managed for
conservation by the Puerto Rico DNER, and collection of any plant in
these lands is regulated by Commonwealth Law No. 133. Currently, there
are permits to collect plants in the Carite and Gu[aacute]nica
Commonwealth Forests. However, such permits are issued by DNER after
determining that proposed actions will not negatively affect the
species (Jos[eacute] Sustache, DNER, pers. comm., 2013; see Factor D
discussion, below). If this proposed rule is adopted, collection of
Varronia rupicola at the Vieques National Wildlife Refuge will require
a special use permit and section 7 consultation (see Factor D
discussion, below).
Summary of Factor B
Agave eggersiana is recognized as an ornamental plant, and is
locally distributed by botanical gardens (St. George Village Botanical
Garden) and the St. Croix Environmental Association to residents for
use in private gardens. Therefore, we consider collection to be a
threat to the species due to the few remaining natural populations.
Overcollection from natural populations may compromise the natural
recruitment and the recovery of Agave eggersiana. We do not believe
that overcollection is a threat to Gonocalyx concolor or Varronia
rupicola.
Factor C. Disease or Predation
Agave eggersiana
The genus Agave is widely affected by the agave snout weevil
(Scyphophorus acupunctatus). This weevil has a wide distribution that
includes the Greater Antilles (i.e., Cuba, Jamaica, Hispaniola, and
Puerto Rico) (Vaurie 1971, p. 4; Setliff and Anderson 2011, p. 1). The
larvae of this weevil feed on the starchy base of the plant, increasing
the risk of infestation by pathogens such as a virus or fungus, later
resulting in the death of the plant (Vaurie 1971, p. 4). At this
[[Page 62571]]
time, there is no information about the occurrence of the agave snout
weevil within St. Croix. However, it has been documented to be found on
adjacent islands such as St. Thomas and Water Island (USVI--https://www.uvi.edu/community/cooperative-extension-service/agriculture-and-natural-resources/integrated-pest-management.aspx).
Although we do not have evidence on the agave snout weevil's
presence on St. Croix, due to the low number of natural populations of
Agave eggersiana and the abundance of vectors (i.e., nonnative agaves
planted in gardens), we consider that the weevil's arrival to this
island is forthcoming. The agave snout weevil's presence on nearby
islands is a concern especially where there is constant traffic
(commuting) among islands with local and international trade. This
could potentially increase the risk of this weevil to arrive and infest
the island at any time. Moreover, the island of St. Croix harbors other
types of Agave, which could potentially become stepping stones for the
weevil to spread around and affect the few and limited populations of
A. eggersiana.
Service biologists documented that a small number of individuals of
Agave eggersiana were observed with scarring along the borders of some
leaves (O. Monsegur and M. Vargas, Service, pers. obs., 2010). It
appears that an insect or arthropod larva may feed on these leaves.
However, the exact cause and the consequences of the scarring remain
unknown. Nevertheless, this is important and should be monitored, as it
might be an indicator of a recently arrived pest to St. Croix.
On Mona Island, Puerto Rico, feral pigs are known to uproot
juveniles and destroy the root system of Agave sisalana (sisal) to feed
on the root system or to use them as a water source (J. Saliva,
Service, pers. obs, 1983 and 1996.). As introduced pigs, donkeys, and
goats have been reported on St. Croix, we cannot disregard the possible
predation of Agave eggersiana, particularly young plants, by these
feral animals. The absence of evidence of predation by these species
might be the result of the low number of individuals of A. eggersiana,
their isolation, and the proximity of some of these populations to
human-inhabited areas. Nonetheless, at this time there is no evidence
that donkeys, pigs, or goats constitute a direct threat to A.
eggersiana.
Gonocalyx concolor and Varronia rupicola
No insect pest or predation of individuals of Gonocalyx concolor or
Varronia rupicola has been documented in the wild. Minor to moderate
infestation by glasshouse whitefly (Trialeurodes vaporariorum) was
observed on cultivated material of V. rupicola at the Royal Botanical
Garden, KEW (Wenger et al. 2010). However, this was suspected to be the
result of the proximity of the V. rupicola material to a species that
is highly susceptible to this insect pest.
Due to the low number of individuals and populations of these
species, disease and predation could certainly be threats. However, we
have no further information indicating that disease or predation are a
current threat to Gonocalyx concolor or Varronia rupicola. We do not
consider disease or predation to be a threat to either of the two
species.
Conservation Efforts To Reduce Disease or Predation
Agave eggersiana, Gonocalyx concolor, and Varronia rupicola
Based on the information available, we have no evidence of
conservation efforts to prevent or reduce adverse effects due to
disease or predation. So far, the only species that could be
potentially affected by an insect pest is Agave eggersiana. However, to
our knowledge, no conservation measure has been implemented in this
regard.
Summary of Factor C
Predation (scaring) has been observed in some individuals of Agave
eggersiana, but there is no direct evidence that the severity of this
stressor has affected the species. However, disease caused by the agave
snout weevil could potentially affect A. eggersiana at a population
level. Thus, based on our analysis of the best available scientific and
commercial available data, we find that disease may be a significant
stressor to the overall status of A. eggersiana by affecting the long-
term survival of the species.
We have no information indicating that disease or predation is a
current threat to Gonocalyx concolor or Varronia rupicola.
Factor D. The Inadequacy of Existing Regulatory Mechanisms
Under this factor, we examine whether existing regulatory
mechanisms are inadequate to address the threats to Agave eggersiana,
Gonocalyx concolor, and Varronia rupicola discussed under other
factors. 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 and 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 Agave eggersiana, Gonocalyx concolor, and Varronia
rupicola.
Agave eggersiana
Territory
The Territory of the U.S. Virgin Islands currently considers Agave
eggersiana as endangered under the Virgin Islands Indigenous and
Endangered Species Act (Law No. 5665) (V.I. Code, Title 12, Chapter 2).
This law, signed in 1990, amended an existing regulation (Bill No. 18-
0403) to provide for the protection of endangered and threatened
wildlife and plants by prohibiting the take, injury, or possession of
indigenous plants. As we mentioned above, A. eggersiana is currently
being used for private landscaping on St. Croix. At present, we do not
have information about the sources of the individuals used for such
purposes. However, we are concerned about the removal of individuals
from natural populations for landscaping. Based on the number of
individuals currently used for private gardens and the landscape
practices in private areas, such as pruning and mowing of populations,
we believe that protection provisions under local regulation may not be
appropriately enforced. Rothenberger et al. (2008, p. 68) indicated
that the lack of management and enforcement capacity continues to be a
significant challenge for the USVI, because enforcement agencies are
chronically understaffed and territorial resource management offices
experience
[[Page 62572]]
significant staff turnover, particularly during administration changes.
Based on the above, although there is a regulatory mechanism that
protects Agave eggersiana on St. Croix, we consider that the
enforcement of the mechanism is inadequate.
Gonocalyx concolor and Varronia rupicola
Federal
One of the currently known populations of Varronia rupicola lies
within the Vieques NWR (Puerto Ferro population). Collecting and
managing plant material (including seeds) within a national wildlife
refuge are regulated and require a permit from the refuge manager (FWS
Form 3-1383-R). The National Wildlife Refuge System Administration Act
of 1966 (16 U.S.C. 668dd-668ee, as amended by the National Wildlife
Refuge System Improvement Act of 1997) provides guidance for management
and public use of the refuge system.
Commonwealth
In 1999, the Commonwealth of Puerto Rico approved the Law No. 241,
also known as New Wildlife Law of Puerto Rico (``Nueva Ley de Vida
Silvestre de Puerto Rico''). The purpose of this law is to protect,
conserve, and enhance both native and migratory wildlife species,
including plants; declare all wildlife species within its jurisdiction
as property of Puerto Rico; and regulate permits, hunting activities,
and nonnative species, among others. However, as we mentioned above
under the Factor A discussion, some individuals of Gonocalyx concolor
and Varronia rupicola have been pruned, and in some cases eliminated,
as result of unauthorized activities such as vegetation removal within
the Commonwealth Forest (O. Monsegur, UPRM, unpubl. report, 2006, p. 1)
and within privately owned lands (Monsegur and Breckon 2007, p. 6).
Therefore, we believe that protection provisions under the Law No. 241
are not being appropriately enforced.
In 1998, the Commonwealth of Puerto Rico approved the Commonwealth
Law No. 150, known as Puerto Rico Natural Heritage Law (Ley del
Programa de Patrimonio Natural de Puerto Rico). The purpose of the Law
No. 150 is to create the DNER Natural Heritage Program. This program
has the responsibility to identify and designate as critical elements
some rare, threatened, or endangered species that should be considered
for conservation, because of their contribution to biodiversity and
because of their importance to the natural heritage (DNR 1988, p.1).
Currently, Gonocalyx concolor and Varronia rupicola are considered as
critical elements by the DNER Natural Heritage Program. The Law No. 150
does not provide penalties for actions that may adversely affect
critical elements; however, the law triggers other Commonwealth laws
and regulations, such as Law No. 133 and Regulation No. 6769 (see
below), that provide protection to critical elements.
The Carite and Gu[aacute]nica Commonwealth Forests are protected by
Law No. 133 (12 L.P.R.A. sec. 191), 1975, as amended, known as the
Puerto Rico Forest Law (``Ley de Bosques de Puerto Rico''), as amended
in 2000. Section 8(A) of Law No. 133 prohibits cutting, killing,
destroying, uprooting, extracting, or in any way damaging any tree or
vegetation within a Commonwealth forest without authorization of the
Secretary of the DNER. Although management plans for Commonwealth
forests include the protection and conservation of species classified
under DNER regulations as critical element, endangered, or threatened,
on occasions the location of such species in the forests makes
enforcement of these regulations a difficult task. As previously
mentioned, Gonocalyx concolor and Varronia rupicola are located
adjacent to trails, near access roads, and below power lines, where
they are susceptible to maintenance practices. According to DNER forest
managers, on several occasions, coordination between forest personnel
and field staff from PREPA has not been effective to avoid damaging
species protected by Commonwealth laws, including V. rupicola and G.
concolor (M. Canals, DNER, pers. comm. 2008; H. Serrano-Delgado, DNER,
pers. comm. 2013).
In 2004, the Commonwealth of Puerto Rico adopted Regulation No.
6769, Regulation of Special Permits for the Use of Communications and
Buildings Associated to Electronic Systems of Communication within
Commonwealth Forests in Puerto Rico (``Reglamento de Permisos
Especiales para Uso de Comunicaciones y Edificaciones Asosiadas a
Sistemas Electr[oacute]nicos de comunicaci[oacute]n en los Bosques
Estatales''), which provides guidance for the installation and
maintenance of telecommunication facilities within Commonwealth forests
and for the protection of natural resources. Article 7(d) of this
regulation states that during installation, operation, and maintenance
of telecommunication facilities, conservation measures should be taken
to avoid or minimize impacts on species protected by DNER and Federal
agencies (DNER 2004a, p. 13). However, individuals of Gonocalyx
concolor have been affected by maintenance activities of existing
communication facilities, making implementation of this regulation a
challenging task (see discussion under Factor A, above, and Factor E,
below).
In 2004, DNER approved Regulation 6766 to regulate the management
of threatened and endangered species in the Commonwealth of Puerto Rico
(``Reglamento para Regir el Manejo de las Especies Vulnerables y en
Peligro de Extinci[oacute]n en el Estado Libre Asociado de Puerto
Rico''). Article 2.06 of Regulation 6766 prohibits collecting, cutting,
and removing, among other activities, listed plants within the
jurisdiction of Puerto Rico. Gonocalyx concolor and Varronia rupicola
are not included in the list of protected species under Regulation
6766. However, as indicated above, Law No. 241 provides protection to
all wildlife species (including plants) under Commonwealth
jurisdiction, even those on private lands.
Local Ordinances
On the island of Anegada, there are various conservation and
education efforts taking place for the protection of rare plant and
animal species (Wenger et al. 2010, p. 8). However, we are unaware of
any formal regulatory mechanism for protecting Varronia rupicola. On
November 3, 1999, a portion of western Anegada (2,646 ac (1,071 ha))
was designated as a Ramsar site and added to the List of Wetlands of
International Importance (Western Salt Ponds of Anegada). A portion of
the preferred limestone habitat of V. rupicola lies within this site,
which is owned by the British government. Although this designation
does not necessarily provide legal protection status, the purpose of
Ramsar sites is to ensure the perpetuation of ecological functions of
those sites by means of a wise-use approach.
Summary of Factor D
Agave eggersiana, Gonocalyx concolor, and Varronia rupicola and
their habitats are partially protected by Federal, Commonwealth,
Territory, and local regulations. However, after evaluating the
information available on the implementation of the existing laws, we
determined those regulatory mechanisms do not provide adequate
protection to the species. The enforcement of existing laws has not
been effective, because harming or injuring (mowing or pruning) Agave
eggersiana has been reported. In addition, the implementation and
[[Page 62573]]
enforcement of effective measures to protect individuals of V. rupicola
located adjacent to existing trails and below power lines within
Commonwealth forests have not been effective. The same problem has
occurred with G. concolor during maintenance of communication towers.
Additionally, it is important to note that enforcement on private lands
continues to be a challenge, as accidental damage or extirpation of
individuals has occurred due to lack of knowledge of the species by
private landowners.
Factor E. Other Natural or Manmade Factors Affecting Their Continued
Existence
Invasive Species
Invasive plant species can affect native ecosystems at three
levels: the genetic level, where the number of individuals of native
species can be reduced below the minimum necessary for persistence; the
species diversity level, where the number of species present and their
distribution can be reduced; and the ecosystem level, where the
functioning of the ecosystem can be changed (Rippey et al. 2002, p.
170). Nonnative species can be very aggressive and compete with native
species for sunlight, nutrients, water, and ground cover. Once
established, these nonnative species typically dominate the landscape,
and the novel forest is characterized by a decrease in the number of
endemics (Lugo and Helmer 2003, p. 145). The impacts of invasive
species are among the greatest threat to the persistence of native rare
species and their habitats (Thomson 2005, p. 615).
Varronia rupicola and Agave eggersiana
Although invasive plant species have not been documented as a
current threat to Varronia rupicola, they may become so in the future.
Studies conducted within the Gu[aacute]nica Commonwealth Forest
indicate that some nonnative tree species (e.g., Leucaena leucocephala)
can persist as a dominant canopy species for at least 80 years (Wolfe
2009, p. 2). The same is expected to occur with nonnative grass species
(e.g., Megathyrsus maximus). These invasive species may invade recently
disturbed (naturally or by human impacts) areas and occupy the suitable
habitat of V. rupicola. Despite the quality and overall diversity of
the habitat that harbors V. rupicola populations in the southern coast
of Puerto Rico, recent developments and habitat fragmentation have
served as corridor for invasive species (e.g., right-of-way for the
former Gasoducto Sur; O. Monsegur, Service, pers. obs., 2013). On the
island of Anegada, numerous invasive plants have been documented in the
town of The Settlement, three of which have been observed moving
towards natural habitats (McGowan et al. 2006, p. 4), further promoting
the risk of wildfires that can affect V. rupicola.
With respect to Agave eggersiana, the populations at Protestant
Cay, Gallows Bay, and Great Pond are surrounded by dense stands of
different species of Sansevieria, an herb native to Africa. This
invasive species seems to be occupying the ecological niche adjacent to
known populations of A. eggersiana (O. Monsegur, Service, pers. obs.,
2013). This invasive species can constrain the number of individuals of
A. eggersiana and reduce the species' limited populations even more.
Gonocalyx concolor
Invasive, native plants, such as the ferns Gleichenella pectinata
and Sticherus bifidus, may invade and alter diverse native communities,
often resulting in plant monocultures that support few wildlife species
(Walker et al. 2010, p. 627). These ferns can colonize disturbed areas
faster than other native plants and may grow into dense mats, thereby
excluding native plants (Walker et al. 2010, p. 634). Additionally, the
mats formed by these species serve as fuel for fires and, in fact,
seems to be fire-tolerant. The invasive, nonnative grass Pennisetum
purpureum (elephant grass) is a fire-adapted species that, in dense
growth, can suppress most grasses, herbs, and tree seedlings (J. K.
Francis, ITF, internet data, 2013).
These invasive ferns and grass are currently found occupying areas
disturbed by fire, landslides, and road construction in Cerro La Santa,
and have the potential to affect Gonocalyx concolor by increasing fire
incidences, microclimate, and nutrient cycling of the habitat on which
this species depends. At present, we have no information about the
competitive abilities of G. concolor in such a situation. Therefore,
the effect of invasive species within the G. concolor habitat should be
considered a threat to the species.
Human-Induced Fires
Fire is not a natural event in subtropical dry or moist forests in
Puerto Rico and the U. S. Virgin Islands. The vegetation in the
Caribbean is not adapted to fires, because this disturbance does not
naturally occur on these islands (Brandeis and Woodall 2008, p. 557;
Santiago-Garc[iacute]a et al. 2008, p. 604). Human-induced fires could
modify the landscape by promoting nonnative trees and grasses, and by
diminishing the seed bank of native species (Brandeis and Woodall 2008,
p. 557). In some cases, fires may maintain extensive areas of young
forest and grasslands, slowing the recovery of ecosysems and,
therefore, impairing the delivery of ecosystem services (Brandeis and
Woodall 2008, p. 557). For example, the nonnative Megathyrsus maximus
is well adapted to fires and typically colonizes areas that were
previously covered by native vegetation. Furthermore, the presence of
this species increases the amount of fuel and the intensity of fires.
Therefore, damage caused by fires to the ecosystems, particularly to
juvenile plants, might be irreversible.
Varronia rupicola and Agave eggersiana
Human-induced fires may lead to destruction of the native
vegetation seed bank and may create conditions favorable for the
establishment of nonnative plant species adapted to fires (e.g.,
Leucaena leucocephala and Megathyrsus maximus) that may outcompete
Varronia rupicola and Agave eggersiana. Furthermore, the presence of M.
maximus and other grass species increases the amount of fuel and the
intensity of fires that may affect endemic populations. Seedling
mortality after fires is related to the differences on fuel loads and
the different fire intensities (Santiago-Garc[iacute]a et al. 2008, p.
607). The V. rupicola populations that occur along the municipalities
of Yauco, Pe[ntilde]uelas, and Ponce are susceptible to forest fires,
particularly on private lands where fires are accidentally or
deliberately ignited. Evidence of recent fires within the habitat and
adjacent to known populations of V. rupicola in Pe[ntilde]uelas and
Ponce have been observed by Service biologist Omar Monsegur (2011 and
2013). Varronia rupicola populations within the Gu[aacute]nica
Commonwealth Forest may be protected, as this conservation area has an
active fire control program (M. Canals, DNER, pers. comm. 2008).
Nonetheless, Miguel Canals, Gu[aacute]nica Commonwealth Forest Manager,
indicates that fires still occur in the forest, particularly on the
periphery along roads (Canals, DNER, pers. comm. 2008). Moreover,
accidental fires have been reported below the PREPA power lines
adjacent to known populations of V. rupicola.
On the island of St. Croix, human-induced fires are also frequently
reported, and most of them appear to have been originated close to
existing roads (Chakroff 2010, p. 41). Estate
[[Page 62574]]
Granard, Estate Jack's Bay, and Estate Isaacs Bay are among the areas
identified as fire hotspots (Chakroff 2010, p. 42). One of the extant
populations of Agave eggersiana is found on Estate Granard, and Jack's
Bay and Isaacs Bay Estates are within the historical range for the
species. In fact, from 2006 to 2009, there were between 1 and 6 fires
in these estates (Chakroff 2010, p. 42). Human-induced fires
particularly threaten the A. eggersiana population at Great Pond due to
the abundance of nonnative grasses in this area. Service's personnel in
St. Croix just documented a wild fire affecting the population of
Catesbaea melanocarpa (Claudia Lombard, Service, pers. comm. 2013).
This population is located less than 0.3 mi (0.5 km) from the A.
eggersiana population at Manchenil Bay.
Gonocalyx concolor
Human-induced fire is also a current threat to Gonocalyx concolor
at Cerro La Santa. Areas adjacent to (less than 33 ft (10 m) from) a
population of this species have been affected by such fires (O.
Monsegur, UPRM, unpubl. data, 2006). Fire effects could accelerate the
colonization of invasive plants and change the vegetation composition
of Cerro La Santa (see discussion under Factor A, above). Currently,
Pennisetum purpureum, a nonnative grass, is occupying these areas,
making them vulnerable to human-induced fires. During the dry season
(March through May), the fern Gleichenella pectinata, and other fern
species that have colonized landslides and roadsides, form dense mats
of dry material that serve as fuel for fires. Although Cerro La Santa
is located in the wet forest, fires still occur in the area,
particularly along roads, during the dry season (C. Pacheco, USFWS,
pers. obs. 2013). Due to the small size of G. concolor populations and
their proximity to areas susceptible to human-induced fires, the
Service considers habitat modification by fires as a threat to the
species.
Hurricanes and Climate Change
The islands of the Caribbean are frequently affected by hurricanes.
The U.S. Virgin Islands have been hit by five major hurricanes in
recent years: Hugo (1989), Luis and Marilyn (1995), Lenny (1999), and
Omar (2008). Examples of the visible effects of hurricanes on the
ecosystem include massive defoliation, snapped and wind-thrown trees,
large debris accumulations, landslides, debris flows, altered stream
channels, and transformed beaches (Lugo 2008, p. 368). Successional
responses to hurricanes can influence the structure and composition of
plant communities in the Caribbean islands (Van Bloem et al. 2003, p.
137; Van Bloem et al. 2005, p. 572; Van Bloem et al. 2006, p. 517; Lugo
2000, p. 245). Hurricanes can produce sudden and massive tree
mortality, which is variable among species (Lugo 2000, p. 245). As
endemics to the Caribbean, Varronia rupicola, Agave eggersiana, and
Gonocalyx concolor would be expected to be well adapted to tropical
storms and the prevailing environmental conditions in this geographical
area. However, the resilience of rare and endangered native species
populations may be limited or constricted by the reduced number of
populations and individuals, making the populations vulnerable to
stochastic events.
Varronia rupicola and Agave eggersiana
The reduced number and small size of Varronia rupicola and Agave
eggersiana populations in Puerto Rico and St. Croix, respectively, make
these species susceptible to hurricanes impacts (e.g., extirpation). In
the case of A. eggersiana, the impacts may be exacerbated by the
reproductive biology of the species (i.e., the species depends on
asexual reproduction, plants dying after flowering, and limited
dispersal of bulbils). Therefore, impacts to a population may
compromise its natural recruitment. In addition, for V. rupicola, a
severe hurricane could result in extensive defoliation and could cause
stem damage.
Populations of Varronia rupicola may be threatened by climate
change, which is predicted to increase the frequency and strength of
tropical storms and can cause severe droughts (Hopkinson et al. 2008,
p. 260). Rather than assessing climate change as a single threat, we
examined the potential consequences to species and their habitats that
arise from changes in environmental conditions associated with various
aspects of climate change. For example, climate-related changes to
habitats or conditions that exceed the physiological tolerances of a
species, occurring individually or in combination, may affect the
status of a species. In fact, vulnerability to climate change impacts
is a function of sensitivity, exposure, and adaptive capacity of
species (IPCC 2007, p. 89; Glick and Stein 2010, p. 19). For instance,
severe droughts may compromise seedling recruitment, as they may result
in deaths of small plants, or may compromise the viability of seeds.
Despite the wide distribution of V. rupicola and the number of
populations, the number of individuals per population may be too low to
sustain a positive recruitment of individuals. This may explain the low
number of intermediate-sized, nonreproductive individuals of V.
rupicola observed in Gu[aacute]nica and Ponce, when compared to the
high numbers of young seedlings (Omar A. Monsegur, Service, pers. obs.
2013).
On the island of Anegada, climate-induced sea-level rise could lead
to the extirpation of Varronia rupicola. The preferred habitat of this
species on that island is in lower elevations, and more than 40 percent
of the island is less than 9.8 ft (3 m) above sea level (Wenger et al.
2010, p. 8). Similarly, Agave eggersiana occurs very close to beach
areas in coastal areas. At least two A. eggersiana populations are
located on a coastal cliff, susceptible to coastal erosion and
landslides. Therefore, we believe that cyclonic surges and coastal
erosion associated with hurricanes may significantly affect the
populations located along the coastal areas of St. Croix (i.e.,
Manchenil Bay, South Shore, Cane Garden, Vagthus Point, and Protestant
Cay), due to their proximity to cliffs and the shoreline.
Gonocalyx concolor
The limited distribution and low number of populations (3) and
individuals (172 historically reported) of this species may exacerbate
its vulnerability to natural events such as hurricanes and landslides,
and compromise its continued existence. Damage to higher elevation
forested habitat is usually greater during hurricane events (Weaver
2008, p. 150). Gonocalyx concolor is extremely vulnerable due to its
habitat requirements and the fact that it is usually found growing on
the canopy of the tallest trees in Cerro La Santa and Charco Azul. The
species is usually associated to old trees with abundant vines and
epiphytes that provide horizontal structure for the colonization of the
species (probably a habitat requirement for the germination of seeds).
Hurricane winds often lead to tree defoliation, loss of small and large
branches, and uprooting, resulting in damage to adjacent trees and
understory vegetation. As a result, gaps are produced in the
vegetation, causing temporary changes in the understory microclimate
due to high light levels and temperature (Walker et al. 2010, p. 626).
Therefore, damage to the forest canopy may result in a direct impact to
individuals of G. concolor that may fall to the ground and probably be
outcompeted by pioneer plant species that get established during early
successional stages after hurricanes.
The recovery of elfin forest vegetation after hurricanes is usually
slow, and the
[[Page 62575]]
early regeneration process is dominated by a few species (Weaver 2008,
p. 150). Furthermore, in the absence of knowledge of the reproductive
capacity and ecological requirements of Gonocalyx concolor, it is
difficult to predict its recovery after natural events such as
hurricanes and tropical storms, particularly when the frequency and
intensity of these weather events is expected to increase with climate
change.
The habitat where Gonocalyx concolor occurs is susceptible to
landslides during rain events mostly associated with tropical storms
and hurricanes. Sometimes rainfall reaches 24 in (60 cm) in a single
storm event, causing floods and interacting with topography and
geologic substrate to induce mass wasting events (e.g., landslides;
Lugo 2000, p. 246). In 1998, during Hurricane Georges, a landslide
adversely affected approximately 2 ac (0.8 ha) of elfin forest at Cerro
La Santa (Hecsor Serrano-Delgado, DNER, pers. comm. 2013). A massive
landslide in the area where the species occurs would not only take out
individuals of G. concolor, but would also modify the habitat necessary
for the species and lead to conditions favoring the establishment of
invasive and weedy vegetation that may permanently modify the habitat
and outcompete G. concolor (see invasive species discussion under
Factor E, above). As documented during Hurricane Georges, and based on
the current conditions of the habitat at Cerro La Santa and Charco
Azul, landslides are a current threat to this species. As with Agave
eggersiana and Varronia rupicola (see discussion above), overall impact
and the cumulative effects of climate change are also expected to have
long-term adverse effects on G. concolor. Gonocalyx concolor is
considered a species with very specific ecological requirements and
that occupies biological islands (i.e., dwarf forests on high
elevations of Puerto Rico). Thus, predicted changes on the structure of
the vegetation due to climate change may result in the irreversible
extirpation of the prime habitat for the species.
Low Reproductive Capacity, Highly Specialized Ecological Requirements,
and Genetic Variation
Gonocalyx concolor and Agave eggersiana
Small and isolated populations of rare plants often display reduced
fitness as reduced reproductive output, seedling performance, or pollen
viability (Holmes et al. 2008, p. 1031). In the case of Gonocalyx
concolor, little is known about its reproductive capacity, recruitment,
and genetic variation. The low number of individuals per population of
a monoecious species (both sexes in the same flower), like G. concolor,
suggests it has highly specialized ecological requirements, production
of viable seeds rarely occurs, or there is a pollinator limitation.
Despite the ongoing monitoring of the known population of G. concolor,
no seedling recruitment has been observed in the wild. Knowing the
phenology of a plant showing limited distribution is important in
understanding the species' biology and ecology, such as the timing of
flowering, fruiting, germination and subsequent growth, and
accumulation of biomass in the field (Ruml and Vulic 2005, p. 218).
Additionally, given the extremely limited geographic distribution of G.
concolor, it is likely that its genetic variability is low.
In the case of Agave eggersiana, its reproductive biology is
characterized by its dependence on asexual reproduction (i.e.,
bulbils). Current evidence suggests that the wild and cultivated
populations of A. eggersiana have minimum genetic variation. This would
result in the loss of alleles by random genetic drift, which would
limit the species' ability to respond to changes in the environment
(Honnay and Jacquemyn, 2007, p. 824).
Conservation Efforts To Reduce Other Natural or Manmade Factors
Affecting Their Continued Existence
Varronia rupicola
The staff from the Royal Botanical Garden (KEW) has developed a
germination and cultivation protocol for Varronia rupicola. KEW is also
conducting studies to determine the genetic variation within and among
known populations, and the species' reproductive biology and population
ecology, to develop a management plan for the species (Hamilton, KEW,
pers. comm. 2012). Further preliminary germination experiments have
been conducted in Puerto Rico at the nurseries of the Gu[aacute]nica
Commonwealth Forest and the Cabo Rojo National Wildlife Refuge. The
Service is not aware of any conservations measure for Agave eggersiana
or Gonocalyx concolor.
Summary of Factor E
Agave eggersiana
Based on the above information and due to the reduced number of
populations and individuals, we believe that Agave eggersiana is
currently threatened by natural or manmade factors, including
hurricanes, fires, and competition with nonnative species. Climate
change may exacerbate these habitat threats by increasing the frequency
of fires, droughts, and hurricanes, but to an unknown extent.
Gonocalyx concolor
The primary threats to Gonocalyx concolor are its limited
distribution and highly specialized ecological requirements. Other
potential threats include low reproductive capacity, possible low
genetic variation, effects of vegetation management, hurricanes and
landslides, human-induced fire, and climate change. G. concolor is
susceptible to hurricanes, landslides, and human-induced fire because
it is confined to geographically small areas. Invasive species and
climate change are potential threats that may be expected in the
future. G. concolor could be negatively affected by the increasing
intensity and frequency of hurricanes and tropical storms,
environmental effects resulting from changing climatic patterns. Any
disturbance of vegetation along the road and around the
telecommunication facilities (including landslides) where the species
is found may directly impact individuals and create conditions
favorable for the establishment of invasive species that may alter
(modify) G. concolor habitat.
Varronia rupicola
Varronia rupicola is threatened primarily by human-induced fires
within its prime habitat. Habitat modification by urban development has
promoted the invasion of its habitat by nonnative plant species (e.g.,
grasses) that are typically fire-adapted and, therefore, increase the
chances of fires by providing a higher fuel load in the ecosystem.
Evidence of recent fires has been documented within the municipalities
of Pe[ntilde]uelas and Ponce in areas close to V. rupicola, threatening
these natural populations. Overall, nonnative plants and fires may
result in extirpation of populations of V. rupicola by killing
individuals, limiting natural recruitment, or permanently modifying
habitat and conditions necessary for the species' establishment.
Furthermore, due to the species' limited numbers and distribution,
hurricanes may extirpate entire populations, and in the case of a
highly fragmented habitat, hurricanes may further promote the invasion
of forest gaps by nonnative plant species rather than native pioneers.
Similarly, severe droughts resulting from climate change may compromise
the survival of seedlings and diminish natural recruitment within wild
populations.
[[Page 62576]]
Cumulative Effects: Factors A through E
Agave eggersiana
The limited distributions and small population sizes of Agave
eggersiana make this species very susceptible to further habitat loss
(Factor A), diseases (Factor C), and competition with nonnative species
(Factor E). Hurricanes, human-induced fires, and climate changes
(Factor E) exacerbate current threats to the species. Furthermore,
although the species is protected by territorial law, enforcement still
is a challenge (Factor D), risking the continued survival of the
species. While these threats may act in isolation, it is very likely
that two or more of these stressors (e.g., habitat loss and diseases)
act simultaneously or in combination, resulting in cumulative impacts
to populations of A. eggersiana.
Gonocalyx concolor
The rarity and specialized ecological requirements of Gonocalyx
concolor (Factor E) make this species extremely vulnerable to habitat
destruction or modification (Factor A), and to other natural or manmade
factors, such as low reproductive capacity, possible low genetic
variation, invasive species, hurricanes, landslides, human-induced
fires, and climate change, particularly because it is confined to small
geographical areas (Factor E). Furthermore, implementation and
enforcement of effective measures to protect G. concolor have not
prevented impacts to the species (Factor D). Although the above
mentioned threats may act in isolation, it is very likely that two or
more of these stressors act simultaneously or in combination (e.g.,
hurricanes and landslides; fires and invasion of nonnative plant
species), resulting in cumulative impacts to populations of G.
concolor, challenging its recovery.
Varronia rupicola
Varronia rupicola has a somewhat extended distribution in southern
Puerto Rico. However, the species is represented by small and
fragmented populations, and about half of them occur within private
lands subject to urban development, making the species prone to
destruction, modification, or curtailment of its habitat (Factor A).
Moreover, other natural or manmade factors such as invasive species,
human-induced fires, hurricanes, and climate change (Factor E) also
pose threats to V. rupicola. Furthermore, implementation and
enforcement of regulatory mechanisms to protect the species have not
been effective, particularly because enforcement on private lands
continues to be a challenge (Factor D). Therefore, it is very likely
that cumulative effects of these threats (e.g., poorly implemented
regulatory mechanisms and habitat destruction) result in limitation, or
even local extirpation, of V. rupicola populations.
Proposed Determination
Agave eggersiana
Agave eggersiana is highly threatened by limited habitat and
habitat loss (e.g., construction of roads, and residential and tourist
developments and landscaping (Factor A)) and the potential for a
disease to wipe out the limited populations (Factor C). In addition,
agave is threatened by a high possibility of commercial collection for
ornamental uses (Factor B), and competition with invasive, nonnative
plants, as well as hurricanes and human-induced fires, which are
further exacerbated by climate change (Factor E). Due to lack of
enforcement, existing regulatory mechanisms are not adequately reducing
these threats (Factor D). All of these threats currently occur
rangewide and are likely to continue into the foreseeable future at a
medium to high intensity.
Based on our evaluation of the best available scientific and
commercial information on the species, the significant threats
affecting Agave eggersiana and its habitat, as well as future potential
threats, we have determined the species is in danger of extinction
throughout all of its range. As a result, we find that A. eggersiana
meets the definition of an endangered species. We find that a
threatened species status is not appropriate for A. eggersiana because
the species is very limited in numbers and in populations, and because
threats are current and ongoing, occurring rangewide, and expected to
continue into the future.
Gonocalyx concolor
Gonocalyx concolor has a very limited distribution. According to
our assessment, this species is threatened by habitat destruction or
modification (Factor A) associated with maintenance and potential
expansion of telecommunication facilities, and to other natural or
manmade factors (i.e., low reproductive capacity, possible low genetic
variation, invasive species, hurricanes, landslides, human-induced
fires, and climate change (Factor E)). Due ineffective implementation
and enforcement, existing regulatory mechanisms are not adequately
reducing these threats (Factor D). All of these threats currently occur
rangewide and are likely to continue into the foreseeable future at a
medium to high intensity.
Based on our evaluation of the best available scientific and
commercial information on the species, the significant threats
affecting Gonocalyx concolor and its habitat, as well as future
potential threats, we have determined the species is currently in
danger of extinction throughout all of its range. As a result, we find
that G. concolor meets the definition of an endangered species. We find
that a threatened species status is not appropriate for G. concolor
because the species is already very limited in numbers and distribution
(i.e., it has a contracted range), and the threats are current and
ongoing, occurring rangewide, and expected to continue into the future.
Varronia rupicola
Current evidence indicates that the majority of suitable habitat
and known populations of Varronia rupicola lie within private lands in
southern Puerto Rico (i.e., Yauco, Pe[ntilde]uelas, and Ponce). These
lands are subject to habitat destruction or modification where impacts
to habitat and populations have been documented. Furthermore,
populations located within the Gu[aacute]nica Commonwealth Forest have
been affected by management practices, such as trail and power lines
maintenance (Factor A). Habitat destruction further results in the
intrusion of nonnative plant species that have the potential to
outcompete V. rupicola and create favorable conditions for fire (Factor
E). Furthermore, implementation and enforcement of regulatory
mechanisms to protect the species have not been effective in reducing
these threats, particularly because enforcement on private lands
continues to be a challenge (Factor D). Some of these threats are
occurring presently at a moderate level, and are likely to increase in
the foreseeable future to a high intensity.
We have carefully assessed the best scientific and commercial
information available regarding the past, present, and future threats
to Varronia rupicola, and have determined that the species meets the
definition of a threatened species throughout all of its range. We find
that an endangered species status is not appropriate for V. rupicola
because the species is not currently in danger of extinction, but
likely will be in the future. It has a wide distribution throughout the
Puerto Rican bank (geographical unit that includes the main island of
Puerto Rico, Vieques, Culebra, the USVI (excluding St. Croix) and the
island of Anegada)), has no
[[Page 62577]]
germination problems, develops as reproductive individuals in a
relatively short time period (1 to 2 years under nursery conditions),
and is the subject of propagation and conservation protocols in
development by the staff of the Royal Botanical Garden (KEW).
Therefore, the Service considers that V. rupicola is a species with a
high recovery potential that meets the definition of a threatened
species.
Significant Portion of the Range
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.'' A major part of the analysis of
``significant portion of the range'' requires considering whether the
threats to the species are geographically concentrated in any way. If
the threats are essentially uniform throughout the species' range, then
no portion is likely to warrant further consideration.
Based on the threats to Agave eggersiana and Gonocalyx concolor
throughout their entire known ranges, we find that these species
currently are in danger of extinction throughout all of their ranges,
based on the severity and scope of the threats described above. As
previously discussed, A. eggersiana and G. concolor are proposed for
listing as endangered species, rather than threatened species, because
the major threats are occurring now, and additional threats will impact
them in the near term. The potential impacts to the species would be
severe given their limited known distribution, the small population
sizes at the remaining sites, and the small area occupied by most of
the populations. Because the threats acting over the three species
extend throughout their entire ranges, it is unnecessary to determine
if the species are in danger of extinction throughout a significant
portion of their ranges. We find that the threats to Varronia rupicola
are a result of future development and lack of regulatory mechanisms.
These impacts are not occurring now. Therefore, on the basis of the
best available scientific and commercial information, we propose
listing A. eggersiana and G. concolor as endangered species, and V.
rupicola as threatened species, throughout their ranges in accordance
with sections 3(6) (endangered), 3(20) (threatened), and 4(a)(1) of the
Act.
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 the species, results in public
awareness and conservation by Federal, State, Tribal, and local
agencies; private organizations; and individuals. The Act encourages
cooperation with the States and requires that recovery actions be
carried out for all listed species. The protection required by Federal
agencies and the prohibitions against certain activities are discussed,
in part, below.
The primary purpose of the Act is the conservation of endangered
and threatened species and the ecosystems upon which they depend. The
ultimate goal of such conservation efforts is the recovery of these
listed species, so that they no longer need the protective measures of
the Act. Subsection 4(f) of the Act requires the Service to develop and
implement recovery plans for the conservation of endangered and
threatened species. The recovery planning process involves the
identification of actions that are necessary to halt or reverse the
species' decline by addressing the threats to its survival and
recovery. The goal of this process is to restore listed species to a
point where they are secure, self-sustaining, and functioning
components of their ecosystems.
Recovery planning includes the development of a recovery outline
shortly after a species is listed and preparation of a draft and final
recovery plan. The recovery outline guides the immediate implementation
of urgent recovery actions and describes the process to 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 identifies site-
specific management actions that set a trigger for review of the five
factors that control whether a species remains endangered or may be
downlisted or delisted, and methods for monitoring recovery progress.
Recovery plans also establish a framework for agencies to coordinate
their recovery efforts and provide estimates of the cost of
implementing recovery tasks. Recovery teams (composed of species
experts, Federal and State agencies, nongovernmental organizations, and
stakeholders) are often established to develop recovery plans. When
completed, the recovery outline, draft recovery plan, and the final
recovery plan will be available on our Web site (https://www.fws.gov/endangered), or from our Caribbean Ecological Services Field Office
(see FOR FURTHER INFORMATION CONTACT).
Implementation of recovery actions generally requires the
participation of a broad range of partners, including other Federal
agencies, States, Tribes, nongovernmental organizations, businesses,
and private landowners. Examples of recovery actions include habitat
restoration (e.g., restoration of native vegetation), research, captive
propagation and reintroduction, and outreach and education. The
recovery of many listed species cannot be accomplished solely on
Federal lands because their range may occur primarily or solely on non-
Federal lands. To achieve recovery of these species requires
cooperative conservation efforts on private and Commonwealth and
Territory lands.
If these species are listed, funding for recovery actions will be
available from a variety of sources, including Federal budgets, State
programs, and cost share grants for non-Federal landowners, the
academic community, and nongovernmental organizations. In addition,
pursuant to section 6 of the Act, the Territory of the U.S. Virgin
Islands and the Commonwealth of Puerto Rico would be eligible for
Federal funds to implement management actions that promote the
protection or recovery of Agave eggersiana, Gonocalyx concolor, and
Varronia rupicola. Information on our grant programs that are available
to aid species recovery can be found at: https://www.fws.gov/grants.
Although Agave eggersiana, Gonocalyx concolor, and Varronia
rupicola are only proposed for listing under the Act at this time,
please let us know if you are interested in participating in recovery
efforts for 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 recovery planning purposes (see FOR
FURTHER INFORMATION CONTACT).
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is 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
[[Page 62578]]
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 formal 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 (Vieques National Wildlife Refuge), and National Park Service
(SARI and Buck Islands Monument); issuance of section 404 Clean Water
Act (33 U.S.C. 1251 et seq.) permits by the U.S. Army Corps of
Engineers; and construction and maintenance of roads or highways by the
Federal Highway Administration.
The Act and its implementing regulations set forth a series of
general prohibitions and exceptions that apply to endangered and
threatened plants. The prohibitions of section 9(a)(2) of the Act,
codified at 50 CFR 17.61, apply to endangered plants. These
prohibitions, in part, make it illegal for any person subject to the
jurisdiction of the United States to import or export, transport in
interstate or foreign commerce in the course of a commercial activity,
sell or offer for sale in interstate or foreign commerce, or remove and
reduce the species to possession from areas under Federal jurisdiction.
In addition, for plants listed as endangered, the Act prohibits the
malicious damage or destruction on areas under Federal jurisdiction and
the removal, cutting, digging up, or damaging or destroying of such
plants in knowing violation of any State law or regulation, including
State criminal trespass law. It is also unlawful to violate any
regulation pertaining to plant species listed as endangered or
threatened (section 9(a)(2)(E) of the Act).
We may issue permits to carry out otherwise prohibited activities
involving endangered and threatened species under certain
circumstances. Regulations governing permits are codified at 50 CFR
17.62 for endangered plants, and at 17.72 for threatened plants. With
regard to endangered plants, a permit must be issued for the following
purposes: for scientific purposes or to enhance the propagation or
survival of the species.
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. The following activities could potentially result
in a violation of section 9 of the Act; this list is not comprehensive:
(1) Unauthorized collecting, handling, possessing, selling,
delivering, carrying, or transporting of Agave eggersiana, Gonocalyx
concolor, or Varronia rupicola, including import or export across State
lines and international boundaries, except for properly documented
antique specimens of these taxa at least 100 years old, as defined by
section 10(h)(1) of the Act;
(2) Introduction of nonnative species that compete with or prey
upon Agave eggersiana, such as the introduction of the nonnative agave
snout weevil to the island of St. Croix, USVI; and
(3) The unauthorized release of biological control agents that
attack any life stage of Agave eggersiana, Gonocalyx concolor, or
Varronia rupicola.
Questions regarding whether specific activities would constitute a
violation of section 9 of the Act should be directed to the Caribbean
Ecological Services Field Office (see FOR FURTHER INFORMATION CONTACT).
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. We have invited these peer reviewers to
comment during this public comment period.
We will consider all comments and information we receive during the
comment period on this proposed rule during our preparation of a final
determination. Accordingly, the final decision may differ from this
proposal.
Public Hearings
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.
Required Determinations
Clarity of the Rule
We are required by Executive Orders 12866 and 12988 and by the
Presidential Memorandum of June 1, 1998, to write all rules in plain
language. This means that each rule we publish must:
(1) Be logically organized;
(2) Use the active voice to address readers directly;
(3) Use clear language rather than jargon;
(4) Be divided into short sections and sentences; and
(5) Use lists and tables wherever possible.
If you feel that we have not met these requirements, send us
comments by one of the methods listed in the ADDRESSES section. To
better help us revise the rule, your comments should be as specific as
possible. For example, you should tell us the numbers of the sections
or paragraphs that are unclearly written, which sections or sentences
are too long, the sections where you feel lists or tables would be
useful, etc.
National Environmental Policy Act (42 U.S.C. 4321 et seq.)
We have determined that environmental assessments and environmental
impact statements, as defined under the authority of the National
Environmental Policy Act (NEPA), 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
Caribbean Ecological Services Field Office (see FOR FURTHER INFORMATION
CONTACT).
Authors
The primary authors of this proposed rule are the staff members of
the Caribbean Ecological Services Field Office.
[[Page 62579]]
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Transportation.
Proposed Regulation Promulgation
Accordingly, we propose to amend part 17, subchapter B of chapter
I, title 50 of the Code of Federal Regulations, as set forth below:
PART 17--[AMENDED]
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; 4201-4245, unless
otherwise noted.
0
2. Amend Sec. 17.12(h) by adding entries for Agave eggersiana,
Gonocalyx concolor, and Varronia rupicola, in alphabetical order under
FLOWERING PLANTS, to the List of Endangered and Threatened Plants to
read as follows:
Sec. 17.12 Endangered and threatened plants.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species
---------------------------------------------------------- Historic range Family Status When Critical Special
Scientific name Common name listed habitat rules
--------------------------------------------------------------------------------------------------------------------------------------------------------
Flowering Plants
* * * * * * *
Agave eggersiana.................. None................. U.S.A. (VI)............. Agavaceae.............. E NA NA
* * * * * * *
Gonocalyx concolor................ None................. U.S.A. (PR)............. Ericaceae.............. E NA NA
* * * * * * *
Varronia rupicola................. None................. U.S.A. (PR); British VI. Boraginaceae........... T NA NA
* * * * * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
* * * * *
Dated: September 3, 2013.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2013-22742 Filed 10-3-13; 8:45 am]
BILLING CODE 4310-55-P