[Federal Register Volume 78, Number 244 (Thursday, December 19, 2013)]
[Proposed Rules]
[Pages 76795-76807]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-29967]
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DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R2-ES-2013-0127; 4500030113]
Endangered and Threatened Wildlife and Plants; 12-Month Finding
on a Petition To List Coleman's Coralroot as an Endangered or
Threatened Species
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Notice of 12-month petition finding.
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SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a
12-month finding on a petition to list Hexalectris colemanii (Coleman's
coralroot) as an endangered or threatened species and to designate
critical habitat under the Endangered Species Act of 1973, as amended
(Act). After review of all available scientific and commercial
information, we find that listing Coleman's coralroot is not warranted
at this time. However, we ask the public to submit to us any new
information that becomes available concerning the threats to the
species or its habitat at any time.
DATES: The finding announced in this document was made on December 19,
2013.
ADDRESSES: This finding is available on the Internet at http://www.regulations.gov at Docket Number FWS-R2-ES-2013-0127. Supporting
documentation we used in preparing this finding is available for public
inspection, by appointment, during normal business hours at the U.S.
Fish and Wildlife Service, Arizona Ecological Services Field Office,
2321 W. Royal Palm Road, Suite 103, Phoenix, AZ 85021. Please submit
any new information, materials, comments, or questions concerning this
finding to the above address.
FOR FURTHER INFORMATION CONTACT: Steve Spangle, Field Supervisor, U.S.
Fish and Wildlife Service, Arizona Ecological Services Field Office,
2321 W. Royal Palm Road, Suite 103, Phoenix, AZ 85021; telephone 602-
242-0210; facsimile 602-242-2513; email incomingazcorr@fws.gov. If you
use a telecommunications device for the deaf (TDD), please call the
Federal Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
In this document we refer to Hexalectris colemanii as Coleman's
coralroot.
Section 4(b)(3)(A) of the Act (16 U.S.C. 1531 et seq.) requires
that, for any petition to revise the Federal Lists of Threatened and
Endangered Wildlife and Plants that contains substantial scientific or
commercial information that listing a species may be warranted, we make
a finding within 12 months of the date of receipt of the petition. In
this finding, we determine whether the petitioned action is: (a) Not
warranted, (b) warranted, or (c) warranted, but immediate proposal of a
regulation implementing the petitioned action is precluded by other
pending proposals to determine whether species are threatened or
endangered, and expeditious progress is being made to add or remove
qualified species from the Federal Lists of Endangered and Threatened
Wildlife and Plants. Section 4(b)(3)(C) of the Act requires that we
treat a petition for which the requested action is found to be
warranted but precluded as though resubmitted on the date of such
finding, that is, requiring a subsequent finding to be made within 12
months. We must publish these 12-month findings in the Federal
Register.
Previous Federal Actions
On June 25, 2007, we received a formal petition dated June 18,
2007, from Forest Guardians (now WildEarth Guardians), requesting that
we list 475 southwest species, including Hexalectris revoluta (Chisos
coralroot), under the Act as either endangered or threatened with
critical habitat. We sent a letter to the petitioner dated July 11,
2007, acknowledging receipt of the petition and stating that the
petition was under review by staff in our Southwest Regional Office.
On December 16, 2009 (74 FR 66866), we determined that we had
substantial information to indicate that listing the Chisos coralroot
as endangered or threatened may be warranted. At that time, we believed
the Chisos coralroot included the entity now known as Coleman's
coralroot. On September 8, 2010, we received a petition dated the same
day from The Center for Biological Diversity requesting that Coleman's
coralroot be listed separately from Chisos coralroot as an endangered
or threatened species under the Act and critical habitat be designated.
We acknowledged receipt of the petition via electronic mail to The
Center for Biological Diversity on September 8, 2010. On December 1,
2011, we sent another letter to The Center for Biological Diversity
acknowledging that Coleman's coralroot was considered a separate
species from the Chisos coralroot as of 2010. In the 2011 letter, we
stated that because the Coleman's coralroot was considered to be a form
of Chisos coralroot in 2009 when we made a substantial 90-day finding
for the Chisos coralroot, we already consider a substantial 90-day
finding to be in place for the Coleman's coralroot, and that we would
further address the petition when workload and funding allow.
On January 30, 2013, we notified interested parties and agencies
that we would be conducting a status review of Coleman's coralroot and
requested information. We received one response letter from Pima
County, AZ. We also informally reached out via email and telephone to
staff at the Coronado National Forest (Coronado NF), WestLand
Resources, Tohono O'odham Nation, and other experts. In addition, on
February 14, 2013, the Service entered into a stipulated settlement
agreement with The Center for Biological Diversity to review the status
of the Coleman's coralroot and submit to the Federal Register a 12-
month finding as to whether listing of the species as an endangered or
threatened species is (a) not warranted; (b) warranted; or (c)
warranted but precluded by other pending proposals, pursuant to 16
U.S.C. 1533(b)(3)(B) by December 31, 2013. This Federal Register
document constitutes our 12-month finding on the September 8, 2010,
petition to list the Coleman's coralroot as an endangered or threatened
species and to designate critical habitat, based on our 2009 positive
90-day finding. This document also fulfills the obligations of the
Service from the February 14, 2013, settlement agreement.
Species Information
Description and Taxonomy
A member of the orchid family (Orchidaceae), Coleman's coralroot is
a perennial herb that forms a short,
[[Page 76796]]
segmented, vertical rhizome or spike. The species has pinkish-cream
stems that measure 46 to 55 centimeters (cm) (18 to 22 inches (in));
inflorescences (flowering part of plant) measure 20 to 23 cm (8 to 9
in) with sepals and petals whitish or creamy-pink to very pale brown at
the tips and partly with noticeable bands of magenta or maroon (Catling
2004, pp. 14-15). The species has a chasmogamous flower (one that opens
to allow for pollination) with a well-developed rostellum (structure
that prevents self-pollination) (Kennedy and Watson 2010, p. 74).
Coleman's coralroot is identifiable by the sepals and lateral petals,
which are rolled back along the outer third of their length by more
than 360 degrees forming a tight coil (Coleman 2002, p. 99).
Coleman's coralroot was originally identified as Hexalectris
spicata from specimens collected by Toolin and Reichenbacher in 1981
and by McLauglin in 1986 (Coleman 1999, pp. 312-14; Coleman 2000
entire; Coleman 2001, p. 96). These specimens were later treated as H.
revoluta by Coleman (1999, pp. 314-315). Using morphological
characteristics (the physical form or structure of an organism or any
of its parts), Catling (2004, pp. 14-16) described H. revoluta var.
colemanii as a variety of H. revoluta. Utilizing phylogenetic analyses
(the assessment of the genetic relatedness of organisms), as well as
morphological characters, Kennedy and Watson (2010, pp. 65, 73-74)
concluded that H. revoluta var. colemanii should be recognized at the
species rank as H. colemanii.
In September of 2010, we solicited independent peer review of the
suggested classification of Hexalectris colemanii by Kennedy and Watson
(2010) as a separate species. Three reviewers opined that Kennedy and
Watson (2010) properly treated H. colemanii as a separate and distinct
species (Jenkins 2010, pers. comm.; Sharma 2010, pers. comm.; Liggio
2010, pers. comm.), while two reviewers opined that, although H.
revoluta var. colemanii is a distinct taxonomic entity at the rank of
variety, it does not merit treatment as a separate species (Goldman
2010, pers. comm.; Freudenstein 2010, pers. comm.). In plant
classification, the use of the term ``variety'' is generally synonymous
with the term ``subspecies''.
Jenkins (2010, pers. comm.) offered that the methods and testing in
Kennedy and Watson (2010) were good and certainly would survive any
criticism from a reviewer who is acquainted with these methods, and
their work showed good evidence that Hexalectris colemanii and H.
arizonicus were reliably different from the other species sampled.
Sharma (2010, pers. comm.) offered that the markers analyzed were
appropriate for the question with regard to whether the different taxa
represent individual taxonomic units or whether they should be
considered single taxonomic units, and it is evident that H. colemanii
stands out as a separate taxonomic unit, i.e., a species, especially
when considered along with the morphological differences that separate
it from its close relatives. Liggio (2010, pers. comm) offered that
Kennedy and Watson (2010) present phylogenetic evidence that H.
colemanii is a distinct taxon, as well as morphological characters that
distinguish it from other members of the Hexalectris spicata complex,
H. revoluta, the western clade of H. spicata and H. arizonica. Goldman
(2010, pers. comm.) offered that Kennedy and Watson (2010) support its
distinction from H. revoluta var. revoluta, but it seems to have
different relationships with various species based upon which phylogeny
is examined (with possible hybridization inferred), and one could also
suspect that it is part of the other new species described in that 2010
paper, H. arizonica, merely as a variety of H. arizonica (or vice-
versa). Freudenstein (2010, pers. comm.) offered that the real
contribution of Kennedy and Watson (2010) has been the addition of
molecular data, but the tree obtained from nuclear locus suggests the
two varieties of H. revoluta are not very distinct from each other.
In conclusion, even though two of our five peer reviewers felt that
Coleman's coralroot should not be treated as a separate species, they
still believe it is a distinct taxonomic entity (i.e., variety).
Furthermore, three reviewers agreed with Kennedy and Watson (2010) that
Coleman's coralroot is a separate and distinct species. Additionally,
the Kennedy and Watson (2010) study that denoted Coleman's coralroot as
a separate species was published in Systematic Botany, which is a peer-
reviewed and widely accepted scientific journal. Based on the
morphological and phylogenetic analysis conducted by Kennedy and Watson
(2010, entire), the fact that this study was published in a peer-
reviewed scientific journal, and because the scientific community has
generally accepted Kennedy and Watson's 2010 determination that the
Coleman's coralroot is a distinct taxonomic entity as noted by our own
peer reviewers, we conclude that the Coleman's coralroot should be
recognized as a separate species. Therefore, based on the best
scientific information available, we recognize Coleman's coralroot
(Hexalectris colemanii) as a distinct species.
Habitat and Life History
Orchids, such as Coleman's coralroot, may be found either as
individual plants or as part of a colony. The determination of what
constitutes a colony, or cluster, is largely based on subjective
professional expertise, taking into consideration factors such as local
geography and relative distance between plants. A colony or cluster can
range from a relatively small number of individual orchids to many
hundred individual plants. A colony or cluster can also span across
areas of varying size and may be primarily interconnected below the
ground level, though this not known with a level of certainty.
Coleman's coralroot grows in moderate shade in oak (Quercus spp.)
woodland canyons, hills, and drainages at elevations between 1,315 to
1,826 meters (m) (4,315 to 5,990 feet (ft)) in southeastern Arizona and
southwestern New Mexico (Coleman 1999, p. 315; 2002, pp. 100-101;
Catling 2004, pp. 15-16; Baker 2012a, p. 9; WestLand Resources 2012a,
pp. 5-7; 2012b, p. 10; 2012c, p. 5; 2012d, pp. 8-10). Though dominated
by oaks, and primarily by white oak (Q. grisea), these woodlands also
include juniper (Juniperus spp.), mesquite (Prosopis spp.), Arizona
black walnut (Juglans major), acacia (Acacia spp.), desert willow
(Chilopsis linearis), and Wright sycamore (Platanus wrightii).
Individual and orchid colonies establish themselves in soil, duff,
humus, and heavy leaf litter under trees such as oak and mesquite, or
among rock outcrops or the edges of rocky cliffs (Coleman 1999, p. 315;
Coleman 2002, p. 101). In a study of general habitat characteristics,
WestLand Resources (2012a, pp. 5-6) found that study sites with
Coleman's coralroot and Hexalectris arizonica (Arizona crested
coralroot) were predominantly characterized by sandy loam or sandy clay
loam soils, had an average 44 percent canopy cover, and slopes ranging
from 1 to 60 percent. This observation is similar to the findings of
Collins et al. (2005, pp. 1,886-1,888), who found that Hexalectris
orchid locations in Texas where statistically correlated with loamy
carbonatic soils and sites with less than 60 percent canopy cover.
Microhabitat parameters appear to vary considerably across known sites
(WestLand Resources 2012d, pp. 9-10), making it difficult to identify
specific conditions needed by the species.
[[Page 76797]]
Plants of the family Orchidaceae are predisposed to
mycoheterotrophy (Kennedy et al. 2011, p. 1,303), meaning they do not
use photosynthesis to make food, but rather obtain food via
relationships with root fungi that have colonized the roots of trees
(Leake 1994, pp. 171-172; Taylor et al. 2003, pp. 1,168-1,169), and
members of the genus Hexalectris are fully mycoheterotrophic (Coleman
2002, p. 91). This mutualism between photosynthetic plants and root
fungi, whereby plants and fungi acquire carbon from one another, is
referred to as mycorrhizal symbiosis. However, mycoheterotrophy in
Hexalectris orchids is entirely one-sided in favor of the orchid, and
they have often been described as parasites. Because Coleman's
coralroot occur predominantly in well-developed white oak woodlands, it
seems likely that the preferred fungus grows on the roots of white oak,
or perhaps in the duff and humus layer near oaks. Hexalectris orchids
exhibit a high degree of mychorrhizal specificity, meaning they have a
very restricted range of fungal associates, and the morphology of
Hexalectris orchids suggests they depend heavily on specific fungi
(Kennedy et al. 2011, pp. 1,309-1,313; Taylor et al. 2003, pp. 1,175-
1,177). Members of the fungal group Sebacinaceae have been identified
as the sole fungal associate of Coleman's coralroot (Kennedy et al.
2011, pp. 1,307-1,313). Although we have no specific information on the
distribution of Sebacinaceae in Arizona, it is reasonable to infer a
wide geographic distribution because Coleman's coralroot associates
with sebacinaceous fungi of widely distant subclades or groups that
have been identified from western Mexico to the eastern United States
(Kennedy et al. 2011, p. 1,313).
Relatively little is known about the reproductive biology of
Coleman's coralroot or other orchids within the genus Hexalectris.
Autogamy (self-pollination) is reported for other members of this
genus, though Coleman's coralroot is considered to be an obligate
outbreeding taxon (relies on cross pollination) with a distinct
rostellum (flower structure that prevents self-pollination) (Argue
2012, p. 144). Argue (2012, p. 144) suggests insects play a role in
pollination of Hexalectris orchids. Hill (2007, p. 15) suggests H.
spicata may require insect pollination because the flowers are
``medium-sized and showy'' and reports observation of a bumblebee
(Bombus impatiens) visiting the flowers of an individual plant in
Indiana. Buchman et al. (2010, pp. 4, 39) suggests that large bees,
such as Bombus and Xylocopa, are likely pollinators of H. warnockii.
Klooster and Culley (2009, pp. 1,340-1,343) found that Bombus spp. were
the most reliable floral visitors and the primary pollen dispersal
agents for two mycoheterotrophic orchids in the subfamily
Monotropoideae. Several species of Bombus have been reported from the
mountains of southern Arizona (Schmidt and Jacobson 2005, pp. 128-129),
and Coleman's coralroot may be pollinated by a member of this genus.
Additionally, the presence of beetles and ants on the flowers of
Hexalectris, including Coleman's coralroot, has been documented (Sharma
2013, pers. comm.). It is not clear if Coleman's coralroot produces
nectar in any significant amount, or if the species could attract
potential pollinators merely through floral scent.
To what degree these orchid colonies exchange genetic material is
unknown, but tiny wind-blown seeds can travel thousands of kilometers
(Jers[aacute]kov[aacute] and Malinov[aacute] 2007, p. 238).
Additionally, the potential for a Bombus pollinator provides some
context to evaluate orchid colony relationships. Although we were
unable to locate information for local Bombus, Carvell et al. (2012, p.
738) reported 2,317 m (7,602 ft) as the maximum foraging distance for
B. pascuorum, a species from Britain, suggesting that colonies within
this distance from one another may exchange genetic material through a
shared pollinator. However, this situation has not been documented for
Coleman's coralroot.
Like most mycoheterotrophs, Coleman's coralroot is almost
exclusively subterranean and survives mostly as an underground tuber or
rhizome (Leake 1994, p. 172; WestLand Resources 2012d, p. 2). For
mycoheterotrophic orchids to reach reproductive maturity may take 10 to
20 years (Hill 2007, p. 16; WestLand Resources 2012c, p. 3), though
Coleman's coralroot likely takes 4 to 10 years (Coleman 2013, pers.
comm.). Researchers suspect that a plant blooms only once then dies,
because rhizomes have been observed to bloom more than once on only a
few occasions (Coleman 2013, pers. comm.). For plants that do bloom
more than once, the period of vegetative dormancy between flowering can
be several years (WestLand Resources 2012c, p. 4). Due to the
uncertainty surrounding maturation and blooming, how long an individual
plant can live is currently unknown.
The total number of blooming individuals fluctuates widely from
year to year and the species is considered an erratic, unreliable
bloomer in successive years (Coleman 2001, p. 96; 2005, p. 250; 2013,
p. 16). Coleman (2002, p. 101) noted that in some years all plants that
send up spikes will put on a good display of flowers, while in other
years none of the plants that sprout will bloom. When individual plants
do bloom, the inflorescence (flowering part of the plant) emerges in
April and flowers bloom between early May and mid-June (Coleman 2002,
p. 101; Catling 2004, p. 15; WestLand Resources 2010, p. 3). The
species sets capsules (seed-bearing structures) very infrequently
(Coleman 2013, p. 18), which may be related to the biology of the
pollinator. Orchids that do successfully set capsules can produce
millions of microscopic seeds that are dispersed by the wind over long
distances and are reliant upon fungi for germination (WestLand
Resources 2012c, pp. 2-3; Hill 2007, p. 17; Leake 1994, p. 172).
Because of the small seed size, individual seeds likely have low
nutrient reserves and seedbanks are likely short-lived.
The quality and quantity of blooming plants in the genus
Hexalectris appears to be influenced by rainfall patterns (Coleman
2002, p. 101; Argue 2012, p. 145). For instance, Collins et al. (2005,
p. 1,888) reported a large number of Hexalectris blooms in Texas
following late spring rains. Engel (2013, p. 2) also reported a
correlation between blooming for H. nitida in Texas and late spring
rains over a 7-year period. For Coleman's coralroot, Coleman (2005, pp.
249-250) found that the number of blooming plants at two sites in
Arizona correlated very closely with winter rains (October to May) from
1996 to 2003. WestLand Resources (2012c, pp. 10-11) demonstrated that
flowering for Coleman's coralroot is highly correlated with October to
March rainfall totals, and hypothesized that flowering may be
positively correlated with cold wintertime temperatures because
wintertime temperatures from 2008 to 2012 were exceptionally low.
Range and Distribution
Coleman's coralroot occurs within oak woodland communities across
southeastern Arizona and southwestern New Mexico. When Coleman's
coralroot was recognized as a separate species in 2010, it was known
only from three sites in the Santa Rita and Dragoon Mountains of
southern Arizona (Center for Biological Diversity 2010, pp. 4-7). Since
that time, extensive surveys have been conducted for the species in
numerous mountain ranges across southeastern Arizona (WestLand
Resources 2010, 2012b, 2012d, 2103, entire). In 2012 alone, WestLand
[[Page 76798]]
Resources (2012b, p. 50) surveyed 181 canyons in 16 mountain ranges. As
of July 2013, the species has been positively identified in 22
confirmed extant colonies across seven mountain ranges, including the
Santa Rita, Whetstone, Dragoon, Chiricahua, Patagonia, Peloncillo, and
Baboquivari Mountains in southeastern Arizona and southwestern New
Mexico (Coleman 2001, p. 96; Catling 2004, p. 15; Coleman 2010, pp. 1-
2; WestLand Resources 2010, pp. 9-14; 2012b, pp. 3-5; 2012d, pp. 4-8;
2013, pp. 5-6). All confirmed extant sites are located on Coronado NF
lands managed by the U.S. Forest Service (USFS) or Tribal lands owned
by the Tohono O'odham Nation.
Population Trends and Abundance
Identifying discrete populations of Coleman's coralroot is
challenging due to the species' life history, particularly its cryptic
nature, the unpredictability of emergence and inflorescence, and the
variability of habitat conditions (e.g., slope, aspect, cover).
Furthermore, we do not have much information on population trends
because most populations were not discovered until after 2010, when the
Coleman's coralroot was recognized as a distinct species. Also, without
specific knowledge of pollinators and gene exchange, making biological
correlations regarding populations is difficult (Baker 2013, pers.
comm.). However, orchids typically occur in patchy distributions where
clusters of plants, or colonies, exhibit some spatial separation
(Tremblay et al. 2006, p. 71; Winkler et al. 2009, p. 995).
Based on our review of the available information, we have
identified 22 confirmed extant colonies (i.e., sites) of Coleman's
coralroot (19 on Coronado NF and 3 on Tohono O'odham Nation). This
includes five colonies in the Santa Rita Mountains in the upper,
middle, and lower McCleary Canyon, Wasp Canyon, and Sawmill Canyon;
three colonies in the Dragoon Mountains including West Cochise
Stronghold, East Cochise Stronghold, and Middlemarch Canyons; four
colonies in the Peloncillo Mountains including Cottonwood Creek in
Arizona, Cottonwood Creek in New Mexico, Miller Spring, and Skeleton
Canyons; two colonies in the Whetstone Mountains including French Joe
and Dry Canyons; four colonies in the Chiricahua Mountains including
upper Tex Canyon, Tex Canyon, and two tributaries to Tex Canyon; one
colony in the Patagonia Mountains in Hermosa Canyon; and three colonies
in the Baboquivari Mountains.
Additionally, four colonies have been identified as to the
coralroot genus Hexalectris, but the actual species were not
identified. These plants had already flowered when they were found
during surveys, so the infloresence had already dried and shriveled.
Without the flower intact, the plants could only be identified to genus
and not to species. However, these findings could potentially be
Coleman's coralroot sites. These include Jordan Canyon in the Santa
Rita Mountains, Paige Creek in the Rincon Mountains, Harshaw Canyon in
the Patagonia Mountains, and Alamo Canyon in the Canelo Hills. If these
are Coleman's coralroot sites, the spatially separated clusters of
plants rise to 26 sites or colonies.
The life history of Coleman's coralroot makes the determination of
population sizes extremely challenging, particularly because individual
plants spend most of their lives underground where they are difficult
to count. It is difficult to estimate population size or trends for
subterranean orchids because the correlation between the number of
rhizomes living underground and the number of spikes that emerge in any
given year is unknown.
To date, monitoring rangewide has been irregular. Prior to 2010
only three Coleman's coralroot colonies had been monitored with
regularity, including McCleary and Sawmill Canyons in the Santa Rita
Mountains, and West Stronghold Canyon in the Dragoon Mountains. These
three sites have been surveyed to varying degrees since 1996 (Coleman
1999, 2000, 2001, 2002, 2005, 2010 entire), and have exhibited
significant fluctuations in the number of orchids emerging year to
year, from zero to dozens of inflorescences. More extensive survey
effort occurred from 2010 through 2013 (WestLand Resources 2013, p. 6),
dramatically increasing the number of known and potential colonies of
Coleman's coralroot. Count data collected for each colony since 2010,
excluding those located on the Tohono O'odham Nation, is presented in
Table 1 (Coleman 2010, p. 4; Baker 2012a, pp. 25-27; WestLand Resources
2010, pp. 9-14; 2012b, pp. 51-55; 2012c, p. 8; 2013, p. 5; Cerasale
2013, pers. comm.).
Table 1--Summary of Total Counts of Inflorescence of Coleman's Coralroot by Colony, 2010-2013
----------------------------------------------------------------------------------------------------------------
Year
Mountain range Canyon ---------------------------------------------------------------
2010 2011 2012 2013
----------------------------------------------------------------------------------------------------------------
Santa Rita.................... Upper McCleary.. 95 6 46 18
Middle McCleary. 15 0 2 6
Lower McCleary.. 10 0 2 2
Wasp............ 4 0 1 0
Sawmill......... 25 6 23 41 (+3*)
Jordan.......... .............. .............. * 4 0
Dragoon....................... West Stronghold. 140 1 31 13
East Stronghold. .............. .............. .............. 1
Middlemarch..... .............. .............. 4 0
Peloncillo.................... Cottonwood Creek .............. .............. 5 0
(AZ).
Cottonwood Creek .............. .............. 2 ..............
(NM).
Miller Spring... .............. .............. 2 5
Skeleton........ .............. .............. 1 0
Whetstone..................... French Joe...... .............. .............. 29 26
Dry............. .............. .............. 1 0
Chiricahua.................... Upper Tex....... .............. .............. .............. 2
Tex............. .............. .............. * 2 4
Tex west .............. .............. .............. 6
tributary.
Tex north .............. .............. .............. 12
tributary.
Patagonia..................... Hermosa......... .............. .............. .............. 1
Paige Creek..... .............. .............. .............. * 16
Rincon........................ Alamo........... .............. .............. .............. * 2
[[Page 76799]]
Canelo Hills.................. Harshaw......... .............. .............. .............. * 1
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* Reported as Hexalectris spp.
Summary of Information Pertaining to the Five Factors
Section 4 of the Act (16 U.S.C. 1533) and implementing regulations
(50 CFR part 424) set forth procedures for adding species to the
Federal Lists of Endangered and Threatened Wildlife and Plants. Under
section 4(a)(1) of the Act, a species may be determined to be
endangered or threatened 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; or
(E) Other natural or manmade factors affecting its continued
existence.
In making this finding, information pertaining to the Coleman's
coralroot in relation to the five factors provided in section 4(a)(1)
of the Act is discussed below. In considering what factors might
constitute threats, we must look beyond the mere exposure of the
species to the factor to determine whether the species responds to the
factor in a way that causes actual impacts to the species. If there is
exposure to a factor, but no response, or only a positive response,
that factor is not a threat. If there is exposure and the species
responds negatively, the factor may be a threat and we then attempt to
determine how significant a threat it is. If the threat is significant,
it may drive or contribute to the risk of extinction of the species
such that the species warrants listing as threatened or endangered as
those terms are defined by the Act. This does not necessarily require
empirical proof of a threat. The combination of exposure and some
corroborating evidence of how the species is likely impacted could
suffice. The mere identification of factors that could impact a species
negatively is not sufficient to compel a finding that listing is
appropriate; we require evidence that these factors are operative
threats that act on the species to the point that the species meets the
definition of threatened or endangered under the Act.
In making our 12-month finding on the petition we considered and
evaluated the best available scientific and commercial information.
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
We have identified mining, livestock grazing, nonnative invasive
plants species, wildfire, drought, and climate change as potential
threats to the habitat or range of the Coleman's coralroot.
Mining
Mining is a significant component of the history and economy of the
American Southwest, particularly Arizona, and there are numerous claims
across the southeastern portion of the State. The Coronado NF, in
particular, has a number of mining proposals in various stages of
planning (Sandwell-Weiss 2012, pers. comm.). Mining and mineral
exploration could detrimentally affect orchids and their habitats
through land clearing, construction of facilities, rock blasting,
groundwater pumping, storm water management, toxic chemical use, and
other mine operations. These activities could directly or indirectly
contribute to: Direct fatality of individual orchids; the loss and
alteration of microhabitat sites necessary for orchid survival; direct
fatality of pollinators; and the loss and alteration of microhabitat
sites necessary for pollinator survival. Of the 22 extant populations,
7 Coleman's coralroot colonies occur within, or adjacent to, mineral
claims on public lands, which include McCleary (3 colonies), Wasp (1
colony), and Sawmill (1 colony) Canyons in the Santa Rita Mountains,
Middlemarch Canyon (1 colony) in the Dragoon Mountains, and Hermosa
Canyon (1 colony) in the Patagonia Mountains (USFS 2011, pp. 374, 393;
Fonseca 2012, pp. 4-5; WestLand Resources 2012c, pp. 1, 17; USFS 2013,
p. 6). We are aware of two mining projects that have developed plans of
operation; the Rosemont Copper Mine in the Santa Rita Mountains, which
may affect colonies in McCleary and Wasp Canyons, and the Hermosa
Drilling Project in the Patagonia Mountains, which may affect a colony
in Hermosa Canyon.
Rosemont Copper Mine--The Rosemont Copper Company has submitted a
mine plan of operation to the Coronado NF for development of the
Rosemont ore deposit. The proposed mine site is located on the east
side of the Santa Rita Mountains of the Nogales Ranger District,
approximately 48 kilometers (km) (30 miles (mi)) south of Tucson,
Arizona. The proposed project would result in the direct disturbance of
approximately 2,839 hectares (ha) (7,016 acres (ac)) of land, including
513 ha (1,267 ac) of private land, 2,287 ha (5,651 ac) administered by
the Coronado NF, 1.2 ha (3 ac) administered by the BLM, and 38 ha (95
ac) of Arizona State Land Department land administered as a State Trust
(SWCA 2012, p. 22). How much of this area is suitable for occupation by
Coleman's coralroot is unknown, largely because the distribution of the
fungal symbiont is unknown. However, the proposed project area is
occupied by two colonies in upper McCleary Canyon and Wasp Canyon.
Project planning is well under way, and the Coronado NF released a
Draft Environmental Impact Statement (EIS) in September 2011. The
Rosemont Copper Mine includes an open-pit copper mine, storage area for
waste rock and tailings, and plant facilities. The mine life, including
construction, operation, reclamation, and closure, is approximately 25
years. The full-scale project is expected to begin after a Final EIS
and a Record of Decision is completed. Based on current scheduling and
compliance, this may occur in late 2013, though the precise schedule
for commencement of the project is not known and depends on the
finalization of the Record of Decision. Construction and operation of
the open pit would entail blasting ore-laden rock with ammonium nitrate
and fuel oil explosive (WestLand Resources 2007, p. 12; USFS 2011, p.
24). Sulfide ore would be transported, via haul trucks, to a series of
crushers and mills to produce finely ground ore, which will be taken to
a flotation processing plant to extract copper concentrate that will
then be loaded for shipment (WestLand
[[Page 76800]]
Resources 2007, pp. 18-20; USFS 2011, p. 25). Waste rock and tailings
will be placed in storage areas primarily on public lands (WestLand
Resources 2007, p. 23; USFS 2011, p. 26).
The Draft EIS acknowledges effects to Coleman's coralroot from the
proposed action, owing to the construction of the mine pit in Wasp
Canyon and the placement of dry-stack tailings in McCleary Canyon (USFS
2011, pp. 393, 405). Based on our review of the available information,
the entirety of two Coleman's coralroot colonies within upper McCleary
and Wasp Canyons lie within the footprint of the preferred alternative
(Barrel) of the proposed Rosemont Copper Mine (USFS 2011, pp. 57-58;
Fonseca 2012, p. 2; WestLand Resources 2012c, p. 21; 2007, p. 2.6). We
anticipate that any and all individual orchids, and their underground
rhizomes, within the direct footprint of the pit, roads, or structures
will be crushed and killed during vegetation clearing, the ore
extraction process (i.e., blasting and crushing), or other operational
activities. Any habitat blasted and transported to the crusher would no
longer remain suitable for orchids. Additionally, we anticipate that
any pollinator nests and hives within the direct footprint of these
facilities would be destroyed. The loss of nearby orchids and
pollinators within the mine footprint could affect the fitness of
orchids remaining on the mine perimeter through a potential reduction
in the exchange of genetic material. However, this effect cannot be
quantified because we cannot predict how many Coleman's coralroot will
be on the mine's perimeter in any given season.
Two orchid colonies, one within middle McCleary Canyon and one
within lower McCleary Canyon, are located just outside the direct
footprint of mine facilities on the northern end of the project site.
They appear to be directly on the edge, or within 305 m (1,000 ft) of
the edge, of the footprint of mine facilities (USFS 2011, p. 58;
WestLand Resources 2012c, p. 21). Due to their proximity, these
colonies could also experience: Drying from denuded vegetation;
increased potential for invasive species, which often favor disturbed
habitats; increased edge effect to the oak stand and fungal
communities; increased vulnerability to predation; alteration of
surface and subsurface hydrology; and exposure to heavy metal
contamination from seepage or fugitive dust. Native floristic quality
can be negatively affected by exposure to heavy metals (Struckhoff et
al. 2013, p. 27), and particulate pollution could lead to physiological
stress of orchids and their habitats that remain on the mine perimeter.
Of particular concern is particle matter that can contain acids,
organic chemicals, metals, and soil or dust particles (USFS 2011, p.
170), because these compounds could potentially be toxic to orchids.
Because fugitive dust from the tailings pile is expected to
generally consist of coarse particles that settle out rapidly (SWCA
2012, p. 20), we do not anticipate exposure to particulates will be
significant. Also, the dust control plan for the mine may include the
application of chemical dust suppressants, such as petroleum resins and
acrylic cement (SWCA 2012, p. 19), which might ameliorate effects to
the two colonies adjacent to the mine. Additionally, the plan of
operation will seek to minimize fugitive dust through implementation of
a variety of controls (e.g., application of binder materials or use of
water spray) (USFS 2011, pp. 196-200). Although the potential for
exposure exists, there is uncertainty regarding the magnitude of these
potential stressors on the two Coleman's coralroot colonies and
habitats located just outside the mine footprint. The level of exposure
cannot be predicted and the specific vulnerability of the species to
these stressors requires further investigation. Furthermore, because
only 4 of the 22 known colonies would be affected by this stressor, we
do not anticipate rangewide impacts to the overall status of the
species. The Coleman's coralroot is known to occur across seven
mountain ranges in southeastern Arizona and southwestern New Mexico,
and we have no information indicating that the remaining colonies are
subject to impacts from mining.
Hermosa Drilling Project--Arizona Minerals, Inc. (AMI) has
submitted a request for approval of a plan of operation to the Coronado
NF to implement the Hermosa Drilling Project. The project area is
located about 9.6 km (6 mi) east of the town of Patagonia, Arizona, on
the Sierra Vista Ranger District, and approximately 80 km (50 mi)
southeast of Tucson, Arizona. The proposed action would extend the
current Hermosa mineral deposit exploration program from AMI patented
mining claims to unpatented claims on Coronado NF lands (AMI 2013, p.
1). Site characterization activities, including mineral exploration
drilling, hydrogeologic drilling and testing, geotechnical drilling and
sampling, and construction and improvement of access roads would
disturb 3.7 ha (9.2 ac) of Coronado NF lands (AMI 2013, p. 9). The
Coronado NF is planning to prepare an Environmental Assessment. The
precise schedule for commencement of the project is not known, though
operations may begin as soon as 2018.
The project area for the Hermosa drilling project overlaps the
occurrence of one individual Coleman's coralroot in Hermosa Canyon and
one individual Hexalectris spp. located near Harshaw Canyon. We assume
this finding represents at least one colony, but we do not have
sufficient information to determine how much land is occupied or if an
entire colony would be affected. However, we anticipate that any
orchids and rhizomes within the direct footprint of exploration
activities would be crushed and killed during vegetation clearing,
drilling, or other operational activities. Additionally, any habitat
modified would no longer maintain suitability for orchids, and any
pollinators within the direct footprint of these activities would be
destroyed. Based on this information, a high level of certainty exists
that at least one individual Coleman's coralroot may be destroyed.
Other Claims--Additional mining claims exist within the known range
of the species. For instance, Coleman's coralroot colonies in the
Dragoon Mountains are located near mining claims. However, we have no
information on whether these lands are closed to new mining claims, if
the Coronado NF will require a plan of operations and an environmental
assessment or environmental impact statement before new disturbance
occurs, or what kind of mining activities can occur prior to Coronado
NF oversight. Thus, we have no specific information regarding other
mining operations that would impact Coleman's coralroot colonies.
In conclusion of mining concerns and based on our review of the
best available information, 7 of the 22 Coleman's coralroot colonies
occur within, or adjacent to, mineral claims on public lands, which
include McCleary (3 colonies), Wasp (1 colony), and Sawmill (1 colony)
Canyons in the Santa Rita Mountains, Middlemarch Canyon (1 colony) in
the Dragoon Mountains, and Hermosa Canyon (1 colony) in the Patagonia
Mountains (USFS 2011, pp. 374, 393; Fonseca 2012, pp. 4-5; WestLand
Resources 2012c, pp. 1, 17; USFS 2013, p. 6). Two Coleman's coralroot
colonies within upper McCleary and Wasp Canyons are likely to be
extirpated by anticipated effects from construction and operation of
the Rosemont Copper Mine, but the five additional colonies are not
expected to be lost. Of these five additional colonies, two colonies in
lower and
[[Page 76801]]
middle McCleary Canyon are likely to be affected by mining operations,
but we have a high level of uncertainty regarding effects to the
viability of those colonies because the effect of adjacent mining
(e.g., fugitive dust) on individual orchids is unknown. Some of the
uncertainty is because a colony may persist underground without
flowering parts emerging. In addition, while at least one and perhaps
two individual orchids within Hermosa and Harshaw Canyons are likely to
be destroyed, we do not know how the viability of a colony or colonies
in those canyons will be affected because we do not know the
distribution of orchids there. Further, other localities of Coleman's
coralroot in the Dragoon Mountains are located near mining claims, but
we have no specific information regarding ongoing or proposed mining
operations in that area or other areas. The existence of a mining claim
does not ensure a mineral deposit will be subject to a plan of
operation or active mining. Therefore, the best available information
indicates that mining does not pose a threat to the Coleman's coralroot
now or in the future.
Livestock Grazing
Cattle grazing in Arizona began in 1696, but ranching did not
proliferate to any extent until the 1870's (Clemensen 1987, p. 1). The
Coronado NF has been managing livestock grazing on its lands since the
early 1900's (Allen 1989, pp. 14-17). Nineteen of the 22 confirmed
extant Coleman's coralroot colonies occur on the Coronado NF within
USFS grazing allotments. Although the Coleman's coralroot is currently
a USFS sensitive species, we do not have any information indicating
that these allotments contain stipulations that protect the species.
Livestock grazing is cited as a contributing factor in the extirpation
of the species from Baboquivari Canyon on BLM lands (Center for
Biological Diversity 2010, p. 10, Coleman 2010, pers. comm.), though
specific evidence is not provided. Hexalectris orchids are palatable to
ungulates, and hoof action could contribute to soil compaction that may
be detrimental to the fungus or the roots of either the Hexalectris or
the oak trees. Livestock grazing has been demonstrated to reduce seed
production and detrimentally impact survival of other orchid species
(Alexander et al. 2010, pp. 47-48). H[aacute]gsater and Dumont (1996,
p. 17) note that heavy grazing and trampling has been shown to
eliminate other species of orchids, reduce plant diversity, and lead to
soil erosion; though they also note that grazing may simulate natural
disturbance regimes, reduce competition, and promote certain rare
species.
In the Whetstone Mountains, French Joe and Dry Canyons that are
occupied by two colonies of Coleman's coralroot are located in the
7,111-ha (17,572-ac) Mescal Allotment, which consists of 4,036 ha
(9,972 ac) capable of supporting grazing. The allotment is permitted
for 800 cattle, or 4,800 Animal Unit Months (AUM), from November 1 to
April 30 of each year (USFS 2010, p. 1; Kraft, 2013, pers. comm.).
Typically, a single herd enters the allotment on November 1, on the
west side and is moved east as feed and water diminish. Cattle travel
to French Joe Canyon on the east side of the allotment at the end of
the grazing season in April.
In the Peloncillo Mountains, one Coleman's coralroot colony occurs
in Skeleton Canyon, which overlaps the 1,594-ha (3,939-ac) Fairchild
Allotment and the 1,882-ha (4,651-ac) Skeleton Allotment which are
together permitted for 272 cattle (1,496 AUM) from October 1 to March
15 of each year (Service 2009, pp. 22, 27; USFS 2008, pp. 2, 21).
Cattle are pushed into upper elevations of the Fairchild Allotment at
the beginning of the grazing season and allowed to drift down to the
north as the season progresses. A lack of reliable water and fencing
makes it difficult to maintain proper distribution, resulting in
heavier use in lower Skeleton Canyon (USFS 2008, p. 273).
In the Dragoon Mountains, the West Cochise Stronghold Canyon, which
is occupied by one colony of Colemen's coralroot, is located within the
4,700-ha (11,616-ac) Slavin Allotment, which consists of 2,030 ha
(5,017 ac) capable of supporting grazing. The allotment is permitted
for 130 cattle (780 AUM) from December 1 to May 31 of each year
(Service 1999, p. 20).
In the Santa Rita Mountains, the 3,931-ha (9,714-ac) Rosemont
Allotment consists of 3,671 ha (9,072 ac) capable of supporting
grazing. The allotment is permitted for 325 cattle from March 1 to 31,
for 325 cattle from September 1 to October 31, and for 150 cattle from
November 1 to February 28 (1,575 AUM) (Service 1999, p. 74).
In the Chiricahua Mountains, the 7,420-ha (18,336-ac) Tex Canyon
Allotment consists of 6,713 ha (16,589 ac) capable of supporting
grazing. The allotment is permitted for 600 cattle from November 1 to
February 28, and 150 cattle from December 1 to February 28 (3,399 AUM)
(Service 1999, p. 66).
As of 2012, the best available information indicates that livestock
grazing occurs within or near all 19 Coleman's coralroot colonies that
exist on Coronado NF lands. Whether livestock grazing occurs near the
three colonies on Tohono O'odham Nation is uncertain, although
information in our files indicates that no cattle activity occurs in
the immediate area of reported plants. However, the presence of
livestock grazing within landscapes where Coleman's coralroot occurs
potentially makes the species vulnerable to direct grazing, trampling,
and compaction of soils. When individual plants do bloom, the
inflorescence (flowering part of plant) emerges in April and flowers
bloom between early May and mid-June (Coleman 2002, p. 101; Catling
2004, p. 15; WestLand Resources 2010, p. 3). Livestock grazing in the
Whetstone and Dragoon Mountains overlaps the emergence season,
providing the opportunity for cattle to eat or trample individual
flowering orchids, or compact soils. Because relevant allotments are
grazed outside the emergence season, cattle have no opportunity to eat
or trample individual flowering orchids in the Peloncillo, Santa Rita,
or Chiricahua Mountains. However, the presence of livestock at other
times does provide the opportunity for cattle to compact soils.
Although cattle are present on the landscape, two key factors
likely contribute to minimization of the effects of grazing on
Coleman's coralroot. First, the Coronado NF has a drought policy that
directs permittees to work with the Coronado NF when rainfall for the
water year (beginning October 1) is less than 75 percent of normal by
March 1 and the long-range forecast is for less than normal
precipitation. This policy limits livestock presence during drought,
which in turn lessens the likelihood that Coleman's coralroot would be
detrimentally impacted by livestock grazing. Second, these allotments
are relatively large allowing livestock to disperse over a large area,
and we have no information to indicate that livestock congregate within
orchid colonies or that they may be attracted to orchid localities.
Livestock grazing has occurred for at least the past 100 years in
Coleman's coralroot habitat. Although livestock grazing has been shown
to affect other species of orchids, Coleman's coralroot persists across
a number of mountain ranges in Arizona and New Mexico despite the
presence of livestock. Because Coleman's coralroots primarily occur in
areas that are not likely to be heavily grazed, such as areas with
thick cover and limited accessibility under oak and mesquite trees,
among rock outcrops, and on the edges of rocky cliffs (Coleman 1999, p.
315; Coleman 2002, p. 101), it is unlikely that
[[Page 76802]]
livestock grazing will substantially impact the orchid. Accordingly,
based on the best available information, livestock grazing does not
pose a threat to the Coleman's coralroot continued existence now or in
the future.
Nonnative Invasive Plant Species
Invasive plants, specifically exotic annuals, can negatively affect
native vegetation including rare plants. One of the most substantial
effects is the change in vegetation fuel properties that, in turn,
alter fire frequency, intensity, extent, type, and seasonality (Menakis
et al. 2003, pp. 282-283; Brooks et al. 2004, p. 677; McKenzie et al.
2004, p. 898) (see Wildfire discussion). Invasive plants can also
exclude native plants and alter pollinator behaviors (D'Antonio and
Vitousek 1992, pp. 74-75; DiTomaso 2000, p. 257; Traveset and
Richardson 2006, pp. 211-213; Cane 2011, pp. 27-28). Furthermore,
invasive plants can out-compete native species for soil nutrients and
water (Aguirre and Johnson 1991, pp. 352-353; Brooks 2000, p. 92), as
well as modify the activity of pollinators by producing different
nectar from native species (Levine et al. 2003, p. 776) or introducing
nonnative pollinators (Traveset and Richardson 2006, pp. 208-209),
leading to disruption of normal pollinator interactions.
Since its introduction in the 1940s, buffelgrass (Pennisetum
ciliare) has become widespread in southeastern Arizona (Yetman 1994,
pp. 1, 8; Van Devender and Reina 2005, p. 161; Cohn 2005, pp. 1-2;
Stevens and Falk 2009, p. 417). Originally introduced as forage for
livestock, as erosion control, or as an ornamental, buffelgrass is now
considered invasive and a threat to native ecosystems (B[uacute]rquez-
Montijo et al. 2002, entire). Researchers generally think that
buffelgrass will continue to spread in the Sonoran Desert biome into
the future, reducing native biodiversity through direct competition and
alteration of nutrient and disturbance regimes (Ward et al. 2006, p.
724; Franklin and Molina-Freaner 2010, p. 1671). However, buffelgrass
is usually limited to elevations less than 1,000 m (3,300 ft) because
it is frost-intolerant (Perramond 2000, p. 5), though it has been
documented up to 1,265 m (4,150 ft) (Arizona Sonora Desert Museum 2012,
p. 2). Coleman's coralroot colonies occur at elevations of 1,315 to
1,826 m (4,315 to 5,990 ft), which is higher than the limit of where
buffelgrass occurs, suggesting the Coleman's coralroot is not impacted
by buffelgrass invasion, though climatic warming trends may facilitate
future invasion of buffelgrass at higher elevations (see Climate Change
discussion).
Other nonnative plant species that may impact Coleman's coralroot's
persistence include Lehman's lovegrass (Eragrostis lehmanniana) and
rose natal grass (Melinis repens) (Baker 2012a, p. 14). However,
specific research is lacking on the impacts of exotic species in
general upon individual Coleman's coralroot and their habitats (Baker
2012a, p. 14). A review of the best available information does not
indicate that Lehman's lovegrass or rose natal grass occurs within
Coleman's coralroot colonies. Also, there is a high level of
uncertainty regarding interactions between these nonnative invasive
species and Coleman's coralroot. Therefore, our review of the best
available information does not indicate that nonnative invasive species
pose a threat to the continued existence of Coleman's coralroot now or
in the future.
Wildfire
Fire frequency and intensity in southwestern forests are altered
from historical conditions (Dahms and Geils 1997, p. 34; Danzer et al.
1997, pp. 1-2). Before the late 1800s, surface fires generally occurred
at least once per decade in montane forests (Swetnam and Baisan 1996,
p. 15). During the early 1900s, frequent widespread ground fires ceased
to occur due to intensive livestock grazing that removed fine fuels,
such as grasses. Coupled with fire suppression, changes in fuel load
began to alter forest structure and natural fire regime (Dahms and
Geils 1997, p. 34). An absence of low-intensity ground fires allowed a
buildup of woody fuels that resulted in infrequent, but very hot,
stand-replacing fires (fires that kill all or most of above-ground
parts of dominant vegetation) (Dahm and Geils 1997, p. 34; Danzer et
al. 1997, p. 9). Additionally, when nonnative buffelgrass invades an
area, the natural fire regime can change from infrequent, low-
intensity, localized fires, to frequent, high-intensity, spreading
fires because of the increased grassy fuel load (Van Devender and Reina
2005, p. 161; Stevens and Falk 2009, p. 418; Yetman 1994, pp. 8-9).
Also, the introduced Lehmans lovegrass can form dense stands,
increasing fine fuels and fire danger where it occurs (Anable et al.
1992, pp. 186-187), which could lead to increased fire hazard in nearby
oak woodlands.
Information in our files indicates wildfires of varying intensity
in the past few years have occurred upslope of Coleman's coralroot
plants on Tohono O'odham Nation. These wildfires may have resulted in
increased runoff from burned areas, which may cause soil erosion that
could wash away Coleman's coralroot plants or bury them under sediment.
However, the available information does not provide specific evidence
that wildfire has directly affected any cluster or colony of Coleman's
coralroot. Additionally, there has been no scientific study of the
impacts of fire on the species (Baker 2012a, p. 13). We can speculate
that native plants that have evolved with low-intensity, high-frequency
wildfire may suffer decreased viability when exposed to a fire regime
that is now dominated by high-intensity wildfire. Hot temperatures may
be too extreme for living plants, existing seedbank, and the pollinator
species; and a hot wildfire occurring during the flowering season could
potentially kill individual orchids that are flowering, or kill oak
trees that are host to the fungal symbiont.
Conversely, Coleman's coralroot life-history traits may provide for
the continued survival of the species under these conditions. Perhaps
the subterranean rhizome is protected from surface fire, allowing the
species to survive and resprout after fire. As discussed above,
buffelgrass and Coleman's coralroot currently occur at different
elevations, reducing the potential for the species to be affected by
fire regimes altered by buffelgrass. Also, the distribution of other
invasive species within or near Coleman's coralroot colonies is
uncertain. Additionally, oak woodlands can recover after hot fires as
affected trees often resprout and grow vigorously, though it may take a
few decades to return to former conditions (Baker 2012a, p. 16).
Overall, researchers have a high level of uncertainty regarding the
effects of wildfire on Coleman's coralroot, and we have no site-
specific information regarding the occurrence of wildfire within or
near sites occupied by Coleman's coralroot. Therefore, our review of
the best available information does not indicate that wildfire poses a
threat to the Coleman's coralroot now or in the future.
Drought and Climate Change
Our analyses under the Act include consideration of ongoing and
projected changes in climate. The terms climate and climate change are
defined by the Intergovernmental Panel on Climate Change (IPCC).
Climate refers to the mean and variability of different types of
weather conditions over time, with 30 years being a typical period for
such measurements, although shorter or longer periods also may be used
(IPCC
[[Page 76803]]
2007, p. 78). Thus, the term climate change refers to a change in the
mean or variability of one or more measures of climate (e.g.,
temperature or precipitation) that persists for an extended period,
typically decades or longer, whether the change is due to natural
variability, human activity, or both (IPCC 2007, p. 78). Various types
of changes in climate can have direct or indirect effects on species.
These effects may be positive, neutral, or negative, and they may
change over time, depending on the species and other relevant
considerations, such as the effects of interactions of climate with
other variables (e.g., habitat fragmentation) (IPCC 2007, pp. 8-14, 18-
19). In our analyses, we use our expert judgment to weigh relevant
information, including uncertainty, in our consideration of various
aspects of climate change.
Climate change will be particularly challenging for biodiversity
because the interaction of additional stressors associated with climate
change and current stressors may push species beyond their ability to
survive (Lovejoy 2005, pp. 325-326). The synergistic implications of
climate change and habitat fragmentation are the most threatening facet
of climate change for biodiversity (Hannah et al. 2005, p. 4). Current
climate change predictions for terrestrial areas in the Northern
Hemisphere indicate warmer air temperatures, more intense precipitation
events, and increased summer continental drying (Field et al. 1999, pp.
1-3; Hayhoe et al. 2004, p. 12422; Cayan et al. 2005, p. 6; Seager et
al. 2007, p. 1181). Climate change may lead to increased frequency and
duration of severe storms and droughts (Cook et al. 2004, p. 1,015;
Golladay et al. 2004, p. 504; McLaughlin et al. 2002, pp. 6,072-6,074).
The current prognosis for climate change in the American Southwest
includes fewer frost days; warmer temperatures; greater water demand by
plants, animals, and people; and an increased frequency of extreme
weather events (Weiss and Overpeck 2005, p. 2,074; Archer and Predick
2008, p. 24). Some models predict dramatic changes in southwestern
vegetation communities (Weiss and Overpeck 2005, p. 2,074; Archer and
Predick 2008, p. 24), especially as wildfires carried by nonnative
plants (e.g., buffelgrass) potentially become more frequent, promoting
the presence of invasive, exotic species over native ones (Weiss and
Overpeck 2005, p. 2,075).
Climate change models predict that the southwestern United States
will become drier in the twenty-first century and that the trend is
already under way (Seager et al. 2007, pp. 1,181-1,184; Schwinning et
al. 2008, p. 14-15). The current, multiyear drought in the southwestern
United States is the most severe drought recorded since 1900 (Overpeck
and Udall 2010, p. 1,642). Winter rainfall in southern Arizona has been
declining steadily for the last 34 years, and most noticeably 1998 to
the present (McPhee et al. 2004, p. 2). Projections predict annual
precipitation in the Southwest will continue to decrease (Christensen
et al. 2007, p. 888; Solomon et al. 2009, p. 1,707). Additionally,
maximum summer temperatures in the Southwest are expected to increase
over time (Christensen et al. 2007, p. 887). Weiss and Overpeck (2005,
p. 2,075) examined low-temperature data over a 40-year timeframe from
numerous weather stations in the Sonoran desert ecoregion and found:
(1) Widespread warming trends in winter and spring, (2) decreased
frequency of freezing temperatures, (3) lengthening of the freeze-free
season, and (4) increased minimum temperatures per winter year. The
current trend in the Southwest of less frequent, but more intense,
precipitation events leading to overall drier conditions is predicted
to continue (Karl et al. 2009, p. 24). The levels of aridity of recent
drought conditions, and perhaps those of the 1950s drought years, will
become the new climatology for the southwestern United States (Seager
et al. 2007, p. 1,181). Additionally, the timing of precipitation may
be altered. Projected patterns of precipitation changes predict that
winter precipitation in the Southwest may decline 10 to 20 percent, for
the period 2090-2099 relative to 1980-1999, as a result of climate
change (IPCC 2007, p. 20).
Arid environments can be especially sensitive to climate change
because the biota that inhabit these areas are often near their
physiological tolerances for temperature and water stress. Slight
changes in temperature and rainfall, along with increases in the
magnitude and frequency of extreme climatic events, can significantly
alter species distributions and abundance (Archer and Predick 2008, p.
23). Nonnative plant species may respond positively, out-competing
native vegetation (Smith et al. 2000, p. 79; Lioubimsteva and Adams
2004, p. 401), thereby increasing the risk of wildfire. Seasonal
changes in rainfall may contribute to the spread of invasive species,
which are often capable of explosive growth, and able to out-compete
native species (Barrows et al. 2009, p. 673).
As discussed above, flowering patterns are highly correlated with
October to March rainfall totals, with higher numbers of flowering
plants observed during years with more winter rainfall. A 10 to 20
percent decline in winter rainfall by the end of this century may have
rangewide repercussions on flowering by Coleman's coralroot, though the
magnitude of effect is uncertain. The irregular flowering patterns of
Coleman's coralroot could already be indicative of effects from
drought. For instance, in a study of the terrestrial orchid
Dactylorhiza majalis, Pavel and Zuzana (1999, pp. 272-273) suggest that
if both climatic and habitat conditions are good, irregular flowering
regimes in orchids should not occur, and such patterns may be
characteristic of sites with declining populations. On the other hand,
flowering in Hexalectris, and Coleman's coralroot in particular, is
known to be very erratic (Hill 2007, p. 16; Coleman 2013, p. 16), and
may be an adaptation to cope with the extreme climatic conditions of
arid environments.
It is difficult to determine how Coleman's coralroot colonies will
fare with current and future drought conditions. The long-term trend
for these colonies is unpredictable, and the inconsistent nature of
historical count data makes it hard to assess trends (e.g., variation
from year to year, unknown relationship to number of rhizomes, and lack
of standardized data collection methodology). Despite past and ongoing
drought conditions, the species continues to persist. While winter
precipitation appears to be correlated with flowering, which influences
seed production and germination, the effects of long-term drought on
these life-history traits are uncertain. Currently, the extent of the
cumulative effects of drought are undocumented, and we have no
information to indicate if they independently or collectively have led
to, or will lead to, the loss of Coleman's coralroot colonies.
It is also possible the Coleman's coralroot is adapted to arid
conditions. Plants growing in high-stress landscapes are often adapted
to stress, and drought-adapted species may experience lower mortality
during severe droughts (Gitlin et al. 2006, pp. 1,477 and 1,484). The
ability of Coleman's coralroot to remain dormant during dry periods,
and regrow when rainfall is abundant, may be an adaptation for coping
with aridity. This ability to remain dormant during dry periods may
have been important in the Coleman's coralroot survival of the large-
scale drought in the 1950s. However, we note that drought was 11 years
and followed by a period of higher
[[Page 76804]]
annual precipitation (Allen and Breschears 1998, p. 14,841; Fye et al.
2003, p. 907), and the current drought may not be comparable.
In summary, the best available information indicates a continuation
of current drying trends, but it does not indicate that the rangewide
status of Coleman's coralroot will be negatively affected. In fact,
some information indicates that Coleman's coralroot is adapted to arid
environmental conditions. Therefore, the best available information
does not indicate that drought and climate change pose a threat to the
Coleman's coralroot at a species-level across the range now or within
the future.
Conservation Efforts To Reduce Habitat Destruction, Modification, or
Curtailment of Its Range
We have no information regarding conservation efforts that are
nonregulatory, such as habitat conservation plans, safe harbor
agreements, habitat management plans, memorandums of understanding, or
other voluntary actions that may be helping to ameliorate stressors to
the species' habitat, but are not legally required.
Summary of Factor A
After assessing the best available science on the magnitude and
extent of the effects of mining, livestock grazing, nonnative invasive
plants species, wildfire, drought, and climate change, we find that the
destruction, modification, and curtailment of Coleman's coralroot's
habitat or range is not a threat to the species. Mining operations may
affect a small percentage of the Coleman's coralroot habitat. Effects
of livestock grazing, nonnative species, wildfire, and drought have not
resulted in measurable population declines. However, a review of the
limited available information does not indicate that these stressors
alone or in combination rise to the level of effects that they would be
considered a threat to the Coleman's coralroot.
Factor B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Coleman's coralroot has been subject to minimal collection related
to documentation of occurrence (i.e., voucher specimens) and scientific
inquiry. Voucher specimens were collected from Baboquivari Canyon by
Toolin in 1981 and from McCleary Canyon by McLaughlin in 1986 (Coleman
2000, p. 138; 2001, p. 96). Specimens were collected from Sawmill
Canyon in 2003 and McCleary Canyon in 2005 for phylogenetic analysis
(Baker 2012a, p. vi; Kennedy and Watson 2010, pp. 64-65; WestLand
Resources 2010, pp. iv-v, 1-2). More recently, voucher specimens were
collected from Cottonwood Creek and Miller Spring by Baker (2012a, p.
vi). WestLand Resources (2012c, p. 5) also reports a collection from
West Cochise Stronghold. These collections represent a small number of
individuals, and there is no indication that large numbers of Coleman's
coralroot have been collected for scientific purposes. In fact, Coleman
(2010, p. 2), the principal authority on the species, reports that he
refrained from collecting the species during his years of survey
effort.
Removal of unsustainable levels of plants from wild populations for
commercial trade is a major cause for the decline of many showy orchids
(H[aacute]gsater and Dumont 1996, p. 9). Although many species of
orchids are highly sought by collectors, we are not aware of any
significant utilization of Coleman's coralroot for commercial or
recreational purposes (i.e., reports or observations of collection or
removal from the wild). Coleman's coralroot localities are relatively
remote and access is challenging, minimizing potential collection by
novices. Furthermore, collection for propagation seems unlikely because
the conditions necessary for growth and survival appear to be very
difficult to recreate in an artificial environment (i.e., successfully
growing the fungus).
Conservation Efforts To Reduce Overutilization for Commercial,
Recreational, Scientific, or Educational Purposes
We have no information regarding conservation efforts that are
nonregulatory, such as habitat conservation plans, safe harbor
agreements, habitat management plans, memorandums of understanding, or
other voluntary actions, that may be helping to ameliorate stressors
due to overutilization for commercial, recreational, scientific, or
educational purposes.
Summary of Factor B
Based on the best available information, the Coleman's coralroot
has been subject to minimal collection. We have no indication that
collection is affecting the species now or will do so in the future.
Therefore, we conclude that overutilization for commercial,
recreational, scientific, or educational purposes, does not pose a
threat to the Coleman's coralroot.
Factor C. Disease or Predation
Orchids like the Coleman's coralroot are susceptible to herbivory
by native browsers, such as insects, small mammals, or deer. Hill
(2007, p. 19) identified herbivory by deer as a potential threat to
Hexalectris orchids, while Baker (2012a, p. 13) offered that Coleman's
coralroot may be vulnerable to predation or grazing by rodents, feral
pigs, rabbits, and deer. Since 1996, evidence of herbivory of Coleman's
coralroot has been observed (Coleman 2013, p. 16), including a report
of a single plant damaged by insects from McCleary Canyon in 1996
(Coleman 1999, p. 314) and the reporting that spikes may be eaten
(Coleman 2002, p. 101). With the dramatic increase in survey effort
from 2010 to 2013, the incidence of observed herbivory also increased.
For instance, in 2010 researchers found that 30 percent of spikes in
West Cochise Stronghold Canyon were browsed by deer (WestLand Resources
2010, p. 12). From the Santa Rita Mountains, WestLand Resources (2012b,
pp. 8, 53-54) reported one Coleman's coralroot inflorescence that
showed signs of herbivory in McCleary Canyon, at least one
inflorescence of H. arizonica that showed insect damage in Agua
Caliente Canyon, and one H. arizonica inflorescence sheared off at the
base due to small rodent or insect herbivory in Dutch John Canyon.
WestLand Resources (2012b, pp. 5, 53) also reported four Hexalectris
spp. in Jordan Canyon in the Dragoon Mountains that appeared to be
clipped from insect herbivory. Baker (2012b, p. 1) also reported an
individual Coleman's coralroot from the Peloncillo Mountains eaten at
the base of the stalk.
In 2012, Coleman (2013, p. 16) marked and tracked eight Coleman's
coralroot plants in Sawmill Canyon, in an effort to quantify the
effects of herbivory. A site visit later that same year revealed four
plants had been destroyed by digging, likely from a small rodent
(Coleman 2013, p. 16). In 2013, all marked plants had either been dug
by a small rodent, or had been eaten down below the lowest flower by
either a rabbit or deer (Coleman 2013, p. 17). Coleman (2013, p. 18)
expressed concern that herbivory may preclude large numbers of plants
from developing and setting capsules. Because the species appears to
set capsules infrequently, herbivory could affect seed development and
dispersal. Coleman (2013, p. 18) concludes that additional work is
needed to identify the herbivores and to determine what
[[Page 76805]]
proportion of plants that emerge in any given year are lost to
herbivory.
As a matter of their life history, wild plants are susceptible to
predation or herbivory. Although it has been demonstrated that
Coleman's coralroot are subject to herbivory, the available information
does not indicate that herbivory is occurring at levels different from
historical conditions or if the species is experiencing population-
level declines or a loss of colony viability as a result of herbivory.
The most significant incident was the documentation of herbivory on 30
percent of spikes in West Cochise Stronghold Canyon in 2010 by WestLand
Resources (2010, p. 12). In 2010, 140 inflorescences were counted in
West Cochise Stronghold that year, the most counted in a single colony.
However, we have no information indicating that herbivory affected
capsule formation for the remaining orchids in West Cochise Stronghold,
and we cannot determine if herbivory has affected the viability of the
colony. Our review of the best available information does not indicate
that herbivory, and resulting loss of individual plants, poses a threat
to the Coleman's coralroot now or in the future.
We have no information regarding specific diseases affecting
Coleman's coralroot, though oak trees can be vulnerable to several
wood-rotting fungi. Oak wilt and oak leaf scorch can be a cause for
concern, but the available information does not indicate that either
occurs in Arizona (Olsen 2013, pers. comm.). Also, the pathogen Nosema
bombi may be responsible for a decline in certain members of bumblebees
in the genus Bombus across the United States. However, several species
remain abundant, and it is unlikely that affected species have become
fully extirpated (Cameron et al. 2010, p. 4). What this means for
Coleman's coralroot is difficult to interpret because the specific
pollinator has not been identified.
Conservation Efforts To Reduce Disease or Predation
We have no information regarding conservation efforts that are
nonregulatory, such as habitat conservation plans, safe harbor
agreements, habitat management plans, memorandums of understanding, or
other voluntary actions, that may be helping to ameliorate stressors
due to disease or predation.
Summary of Factor C
Overall, researchers have uncertainty regarding the effects that
disease and predation have on Coleman's coralroot at the population and
species levels. Accordingly, our review of the best available
information does not indicate that disease or predation poses a threat
to the Coleman's coralroot now or will do so in the future.
Factor D. The Inadequacy of Existing Regulatory Mechanisms
Under this factor, we examine whether existing regulatory
mechanisms are inadequate to address or alleviate the threats to the
species discussed under the 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, plans, regulations, and other such mechanisms that may minimize
any of the threats we describe in threat analyses under the other four
factors, or otherwise enhance conservation of the species. We give
strongest weight to statutes and their implementing regulations and to
management direction that stems from those laws and regulations. An
example would be State governmental actions enforced under a State
statute or constitution, or Federal action under statute. Having
evaluated the significance of the threat as mitigated by any such
conservation efforts, we analyze under Factor D the extent to which
existing regulatory mechanisms are inadequate to address the specific
threats to the species. Regulatory mechanisms, if they exist, may
reduce or eliminate the impacts from one or more identified threats. In
this section, we review existing Federal and State regulatory
mechanisms to determine whether they effectively reduce or remove
threats to Coleman's coralroot.
Federal Regulations
Nineteen of 22 known Coleman's coralroot colonies occur on lands
managed by the USFS as part of the Coronado NF. Although the Coleman's
coralroot is not covered under the Coronado NF's Land and Resource
Management Plan at this time, it does receive indirect benefits from
management strategies outlined in the plan. For instance, the Coronado
NF's Land and Resource Management Plan has guidance to protect riparian
areas, maintain or restore fire-adapted ecosystems through thinning or
prescribed burning, and provide for invasive species management. Any of
these management strategies would provide some ancillary benefit to the
Coleman's coralroot. On the other hand, the species may be affected by
program management activities like grazing, recreation, mining,
invasive species management, and fire management. The Coronado NF's
Land and Resource Management Plan is designed to minimize impacts to
sensitive species from management activities, but actual ground-level
conservation would be implemented during project-specific planning and
implementation.
Also, numerous Federal statutes apply on these lands. Because we
have identified the construction of the proposed Rosemont Copper Mine
as potentially affecting four colonies, two statutes of particular
interest are the Mining Law of 1872 (30 U.S.C. 21 et seq.) and the
National Environmental Policy Act of 1969 (42 U.S.C. 4321 et seq.)
(NEPA). The Mining Law was enacted to promote exploration and
development of domestic mineral resources, as well as the settlement of
the western United States. In addition, the USFS considers the effects
of their actions on the viability of sensitive species through the NEPA
process. As defined by USFS's own policy, actions should not result in
loss of species viability or create significant trends toward the need
for Federal listing. Coleman's coralroot is currently a USFS sensitive
species and is being considered in the planning process for the
Rosemont Copper Mine. At this state in the planning process, we are
unaware of mitigating actions, if any, the USFS may require for
Coleman's coralroot as part of the NEPA process. If the mining project
proceeds as planned, two colonies in upper McCleary and Wasp Canyons
will be lost to the construction and operation. However, other sites
throughout the species' range do not appear to be facing mining or
other threats now or in the future to which current Federal regulations
would apply. Although Federal regulations will not protect the portion
of the species' range in upper McCleary and Wasp Canyons from the
detrimental effects of hard rock mining, we do not find existing
regulatory mechanisms to be inadequate across the entire range of the
species.
Tribal Regulations
We have no information regarding specific Tribal regulations
designed to protect Coleman's coralroot. In October of 2009, the Tohono
O'odham Nation issued a resolution opposing the Rosemont Copper Mine.
However, the Tohono O'odham Nation has no regulatory authority to
manage the effects from this mine, because it does
[[Page 76806]]
not occur on their land. Although we are unaware of any Tribal
regulations that would provide protection to the Coleman's coralroot,
there are no threats on Tribal lands to which regulations would apply.
State Regulations
No State laws specifically protect Coleman's coralroot habitat on
State or private lands in Arizona. Also, the species is currently not
on the list of native plants protected from collection by the Arizona
Native Plant Act (Arizona Department of Agriculture 2013, entire).
Although State of Arizona regulations provide no protection to the
species, we do not find them to be inadequate because no threats exist
to which State regulations would apply.
Summary of Factor D
Based on our review of the best available information, we do not
believe that there are inadequate regulatory mechanisms posing a threat
to the Coleman's coralroot now or will do so in the future.
Factor E. Other Natural or Manmade Factors Affecting Its Continued
Existence
We have evaluated the best available scientific information, and we
did not find any information indicating that recreation, activities
associated with illegal immigration, development, or any other natural
or manmade factors are threats to the Coleman's coralroot. We found no
indication that Coleman's coralroot are trampled, crushed, or destroyed
by off-road vehicles, illegal immigrants, Border Patrol operations, or
housing construction. Additionally, the Coleman's coralroot colonies
may be somewhat protected from these activities because of the rugged
terrain (e.g., steep slopes, thick brush, rock outcrops, the edges of
rocky cliffs) in which they occur. Information in our files indicates
signs of illegal immigration near Coleman's coralroot colonies on
Tohono O'odham Nation, but we have no information indicating that
individual orchids have been destroyed or that the viability of any
colony has been compromised.
We also considered whether small population size and overall rarity
of Coleman's coralroot were threats. We recognize that Coleman's
coralroot may be rare as indicated by the relatively small number of
canyons where the species has been found compared to the large number
of canyons that have been searched. But we did not find any indication
that the rarity of the species, acting in concert with other stressors,
is a threat to the species.
Conservation Efforts To Reduce Other Natural or Manmade Factors
Affecting Its Continued Existence
We have no information regarding conservation efforts that are
nonregulatory, such as habitat conservation plans, safe harbor
agreements, habitat management plans, memorandums of understanding, or
other voluntary actions, that may be helping to ameliorate stressors
due to other natural or manmade factors affecting the Coleman's
coralroot's continued existence.
Summary of Factor E
Based on the best available information, we have determined that
other natural or manmade factors do not pose a threat to the Coleman's
coralroot now or in the future.
Finding
As required by the Act, we conducted a review of the status of the
species and considered the five factors in assessing whether the
Coleman's coralroot is an endangered or threatened species throughout
all or a significant portion of its range. We examined the best
scientific and commercial information available regarding the past,
present, and future threats faced by the species. We reviewed the
petition, information available in our files, and other available
published and unpublished information, and we consulted with
appropriate experts and other Federal and local agencies. In
considering which factors might constitute threats, we must look beyond
the mere exposure of the species to the factor to determine whether the
species responds to the factor in a way that causes actual impacts to
the species. If the species has exposure to a factor, but no response,
or only a positive response, that factor is not a threat. If the
species has exposure and responds negatively, the factor may be a
threat and we then attempt to determine how significant a threat it is.
If the threat is significant, it may drive or contribute to the risk of
extinction of the species such that the species warrants listing as an
endangered or threatened species as those terms are defined by the Act.
This situation does not necessarily require empirical proof of a
threat. The combination of exposure and some corroborating evidence of
how the species is likely impacted could suffice. The mere
identification of factors that could impact a species negatively is not
sufficient to compel a finding that listing is appropriate; we require
evidence that these factors are operative threats that act on the
species to the point that the species meets the definition of
threatened or endangered under the Act.
Under the five-factor analysis above, we identified several
potential stressors that will likely cause declines, such as mining
operations, livestock grazing, wildfire, drought, and herbivory.
However, we have no information to indicate that these stressors alone
or in combination rise to the level of effects that they would be
considered a threat to the species' continued existence. Based on
anticipated mining operations, we expect that 2 of the 22 confirmed
Coleman's coralroot colonies will be extirpated due to mining
operations and that 3 additional colonies may be negatively impacted
but not lost. The Coleman's coralroot is known to occur across seven
mountain ranges in southeastern Arizona and southwestern New Mexico.
Because the species is fairly wide ranging, we do not believe that
mining operations, livestock grazing, wildfire, drought, and herbivory
operate in a manner that results in cumulative synergistic negative
effects at the species level. The best available information does not
indicate that the remaining colonies are subject to operative threats
or that the impacts from any of the stressors are contributing to the
risk of extinction such that the species warrants listing as an
endangered or threatened species. Therefore, based on our review of the
best available scientific and commercial information pertaining to the
five factors, we find that the stressors are not operating at a level
that is resulting in a species-level impact to indicate that Coleman's
coralroot is in danger of extinction (endangered), or likely to become
endangered within the foreseeable future (threatened), throughout all
of its range.
Significant Portion of the Range
Having determined that Coleman's coralroot does not meet the
definition of a threatened or endangered species, we must next consider
whether there are any significant portions of the range where the
Coleman's coralroot is in danger of extinction or is likely to become
endangered in the foreseeable future. A portion of a species' range is
significant if it is part of the current range of the species and it
contributes substantially to the representation, resiliency, or
redundancy of the species. The contribution must be at a level such
that its loss would result in a decrease in the ability to conserve the
species.
In determining whether a species is threatened or endangered in a
significant portion of its range, we first identify any portions of the
range of the species that warrant further
[[Page 76807]]
consideration. The range of a species can theoretically be divided into
portions an infinite number of ways. However, there is no purpose to
analyzing portions of the range that are not reasonably likely to be
both (1) significant and (2) threatened or endangered. To identify only
those portions that warrant further consideration, we determine whether
substantial information indicates that: (1) The portions may be
significant, and (2) the species may be in danger of extinction there
or likely to become so within the foreseeable future. In practice, a
key part of this analysis is whether the threats are geographically
concentrated in some way. If the threats to the species are essentially
uniform throughout its range, no portion is likely to warrant further
consideration. Moreover, if any concentration of threats applies only
to portions of the species' range that are not significant, such
portions will not warrant further consideration.
If we identify portions that warrant further consideration, we then
determine whether the species is threatened or endangered in these
portions of its range. Depending on the biology of the species, its
range, and the threats it faces, the Service may address either the
significance question or the status question first. Thus, if the
Service considers significance first and determines that a portion of
the range is not significant, the Service need not determine whether
the species is threatened or endangered there. Likewise, if the Service
considers status first and determines that the species is not
threatened or endangered in a portion of its range, the Service need
not determine if that portion is significant. However, if the Service
determines that both a portion of the range of a species is significant
and the species is threatened or endangered there, the Service will
specify that portion of the range as threatened or endangered under
section 4(c)(1) of the Act.
In our analysis for this listing determination, we determined that
the Coleman's coralroot does not meet the definition of an endangered
or threatened species throughout its entire range. We found that there
are geographically concentrated stressors. The effects from the
proposed Rosemont Copper Mine (located on the east side of the Santa
Rita Mountains) and Hermosa Drilling Project (located in the Patagonia
Mountains) will be limited to 5 of 22 confirmed extant colonies of
Coleman's coralroot, including 4 colonies located in McCleary and Wasp
Canyons in the Santa Rita Mountains, and 1 located in Hermosa Canyon in
the Patagonia Mountains. Two of these colonies are expected to be
extirpated. Even if these 2 colonies are extirpated, the Coleman's
coralroot will continue to remain in 20 other colonies across 7
mountain ranges. There is enough redundancy in the remaining
populations spread over a wide geographic area that the species will
continue to persist.
Furthermore, determining the effect of the potential loss of these
individual plants on the rangewide status of the species is challenging
because of the lack of information on population ecology and
demographics. For instance, we have no information regarding the degree
to which these populations exchange genetic material, if these two
colonies represent a unique genetic diversity, or the degree to which
they may behave as subpopulations within a metapopulation. There is no
information regarding how the number of aboveground flowering plants
correlates with the total number of orchids, including those living
underground as a rhizome or tuber. Thus, it is very difficult to
determine how resilient the species is to withstanding demographic and
environmental variation. These information gaps and uncertainties make
it difficult to extrapolate population sizes, to evaluate trends, or to
make meaningful comparisons within and across years. Based on the best
available information, we have no evidence to indicate that the two
colonies we expect to be extirpated are a significant portion of the
current range of the species or that they contribute substantially to
the representation, resiliency, or redundancy of the species.
Therefore, we have no information to indicate that the contribution of
five colonies that will be impacted from mining are at a level such
that their loss would result in a decrease in the ability to conserve
the species.
Our review of the best available scientific and commercial
information indicates that the Coleman's coralroot is not in danger of
extinction now (endangered) nor likely to become endangered within the
foreseeable future (threatened) throughout all or a significant portion
of its range. Although we expect two colonies (upper McCleary and Wasp
Canyons) to be severely compromised or lost, and three other colonies
(lower and middle McCleary, and Hermosa Canyons) to be detrimentally
affected, we have no information to indicate that these losses would
have a negative impact on the overall species across its entire range.
Accordingly, we do not find that threats to the portion of the species'
range in McCleary, Wasp, and Hermosa Canyons would likely place the
species in danger of extinction throughout its entire range. Because
the portion of the Coleman's coralroot colonies in these canyons due to
mining is not significant enough that their potential loss would render
the species in danger of extinction now or in the foreseeable future,
we conclude that these colonies do not constitute a significant portion
of the species' range. Therefore, we find that listing the Coleman's
coralroot as an endangered or threatened species under the Act is not
warranted at this time.
We request that any new information concerning the status of, or
threats to, Coleman's coralroot be submitted to our Arizona Ecological
Services Field Office (see ADDRESSES section) whenever it becomes
available. New information will help us monitor the species and
encourage its conservation. If an emergency situation develops for
Coleman's coralroot, or any other species, we will act to provide
immediate protection.
References Cited
A complete list of references cited is available on the Internet at
http://www.regulations.gov and upon request from the Arizona Ecological
Services Office (see ADDRESSES section).
Author(s)
The primary authors of this notice are the staff members of the
Arizona Ecological Services Field Office.
Authority
The authority for this finding is section 4 of the Endangered
Species Act of 1973, as amended (16 U.S.C. 1531 et seq.).
Dated: December 2, 2013.
Rowan W. Gould,
Acting Director, Fish and Wildlife Service.
[FR Doc. 2013-29967 Filed 12-18-13; 8:45 am]
BILLING CODE 4310-55-P