Endangered and Threatened Wildlife and Plants; Determination of Endangered Status for Ipomopsis polyantha (Pagosa Skyrocket) and Threatened Status for Penstemon debilis (Parachute Beardtongue) and Phacelia submutica (DeBeque Phacelia), 45054-45075 [2011-18429]
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Federal Register / Vol. 76, No. 144 / Wednesday, July 27, 2011 / Rules and Regulations
DEPARTMENT OF THE INTERIOR
Previous Federal Actions
Ipomopsis polyantha
We first identified Ipomopsis
polyantha as a taxon under review in
50 CFR Part 17
the 1983 Supplement to Review of Plant
[FWS–R6–ES–2010–0015; MO 92210–0–0008 Taxa for Listing as Endangered or
Threatened Species (48 FR 53640,
B2]
November 28, 1983). In that document,
we included the species as a Category 2
RIN 1018—AV83
candidate, based on our evaluation at
that time. We published our decision to
Endangered and Threatened Wildlife
discontinue candidate categories and to
and Plants; Determination of
restrict candidate status to those taxa for
Endangered Status for Ipomopsis
which we had sufficient information to
polyantha (Pagosa Skyrocket) and
support issuance of a proposed rule on
Threatened Status for Penstemon
December 5, 1996 (61 FR 64481). This
debilis (Parachute Beardtongue) and
resulted in the deletion of Ipomopsis
Phacelia submutica (DeBeque
polyantha from the list of candidate taxa
Phacelia)
for listing. We added the species to the
list of candidates again in the 2005
AGENCY: Fish and Wildlife Service,
Candidate Notice of Review (CNOR) (70
Interior.
FR 24870, May 11, 2005) with a listing
ACTION: Final rule.
priority number (LPN) of 2. A listing
priority of 2 reflects threats that are
SUMMARY: We, the U.S. Fish and
imminent and high in magnitude, as
Wildlife Service (Service), determine
well as the taxonomic classification of I.
endangered status for Ipomopsis
polyantha as a full species. We
polyantha (Pagosa skyrocket), a plant
published a complete description of our
species in Archuleta County, Colorado;
listing priority system in the Federal
threatened status for Penstemon debilis
Register (48 FR 43098, September 21,
(Parachute beardtongue) in Garfield
County, Colorado; and threatened status 1983).
On June 23, 2010, we proposed to list
for Phacelia submutica (DeBeque
Ipomopsis polyantha as endangered (75
phacelia) in Mesa and Garfield
FR 35721). In the proposed rule, we
Counties, Colorado, under the
found that critical habitat for the species
Endangered Species Act of 1973, as
was prudent, but not determinable at
amended (Act). Designation of critical
that time. A proposed rule to designate
habitat for the three species is proposed
critical habitat for this species is being
concurrently in a separate rule in this
published concurrently with this final
edition of the Federal Register.
rule.
DATES: This rule becomes effective on
Penstemon debilis
August 26, 2011.
We first included Penstemon debilis
ADDRESSES: This final rule is available
as a category 2 candidate species in the
on the Internet at https://
February 21, 1990, Review of Plant Taxa
www.regulations.gov. Comments and
materials received, as well as supporting for Listing as Endangered or Threatened
Species (55 FR 6184). When we
documentation used in preparing this
abandoned the use of numerical
final rule are available for public
category designations in 1996, we
inspection, by appointment, during
normal business hours, at U.S. Fish and changed the status of P. debilis to a
candidate under the current definition.
Wildlife Service, Western Colorado
We published four CNOR lists between
Ecological Services Field Office, 764
1996 and 2004, and P. debilis remained
Horizon Drive, Building B, Grand
a candidate species with an LPN of 5 on
Junction, CO 81506–3946; telephone
970–243–2778; facsimile 970–245–6933. each (62 FR 49398, September 19, 1997;
64 FR 57534, October 25, 1999; 66 FR
FOR FURTHER INFORMATION CONTACT: Al
54808, October 30, 2001; 67 FR 40657,
Pfister, Western Colorado Supervisor,
June 13, 2002). An LPN of 5 is assigned
U.S. Fish and Wildlife Service,
to species with non-imminent threats of
Ecological Services Field Office, 764
a high magnitude.
Horizon Drive, Building B, Grand
In the 2005 CNOR (70 FR 24870, May
Junction, CO 81506–3946; telephone
11, 2005), we changed the LPN for
970–243–2778, extension 29; facsimile
Penstemon debilis from 5 to 2 based on
970–245–6933. If you use a
an increase in the intensity of energy
telecommunications device for the deaf
exploration along the Roan Plateau
(TDD), call the Federal Information
escarpment, making the threats to the
Relay Service (FIRS) at 800–877–8339.
species imminent. The CNOR lists
published in 2006, 2007, and 2008
SUPPLEMENTARY INFORMATION:
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maintained P. debilis as a candidate
species with an LPN of 2 (71 FR 53756,
September 12, 2006; 72 FR 69034,
December 6, 2007; 73 FR 75176,
December 10, 2008).
In each assessment since its
recognition as a candidate species in
1996, we determined that publication of
a proposed rule to list the species was
precluded by our work on higher
priority listing actions. In 2008, we
received funding to initiate the proposal
to list Penstemon debilis. In the 2008
notice, we announced that we had not
updated our assessment for this species,
as we were developing a proposed
listing rule (73 FR 75227). On June 23,
2010, we proposed to list P. debilis as
threatened (75 FR 35721). In the
proposed rule, we found that critical
habitat for the species was prudent, but
not determinable at that time. A
proposed rule to designate critical
habitat for this species is being
published concurrently with this final
rule.
Phacelia submutica
We included Phacelia submutica as a
category 1 candidate species in the 1980
Review of Plant Taxa for Listing as
Endangered or Threatened Species (45
FR 82480, December 15, 1980). In that
notice, category 1 candidates were
defined as species for which the Service
had ‘‘sufficient information on hand to
support the biological appropriateness
of their being listed as Endangered or
Threatened species.’’ We changed the
candidate status of P. submutica to
category 2 on November 28, 1983 (48 FR
53640). On February 21, 1990, we again
identified P. submutica as a category 1
candidate species (55 FR 6184). In the
February 28, 1996, Federal Register (61
FR 7596), all category 1 candidate
species became candidates under the
current definition. We assigned P.
submutica an LPN of 11. In the 2005
CNOR (70 FR 24870, May 11, 2005) we
raised the LPN to 8, to reflect the
increasing level of threats, which were
imminent and of moderate magnitude.
On May 11, 2004, we received a
petition from the Center for Biological
Diversity (CBD) to list, as endangered,
225 species we previously had
identified as candidates for listing,
including Phacelia submutica (CBD
2004, p. 146). Under requirements in
section 4(b)(3)(B) of the Act (16 U.S.C.
1531 et seq.), the CNOR and the Notice
of Findings on Resubmitted Petitions
published by the Service on May 11,
2005 (70 FR 24870), included a finding
that the immediate issuance of a
proposed listing rule and the timely
promulgation of a final rule for each of
these petitioned species, including P.
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submutica, was warranted but
precluded by higher priority listing
actions, and that expeditious progress
was being made to add qualified species
to the lists.
On April 28, 2005, the Center for
Native Ecosystems (CNE), the Colorado
Native Plant Society, and botanist Steve
O’Kane, Jr., Ph.D., submitted a petition
to the Service to list Phacelia submutica
as endangered or threatened within its
known historical range, and to designate
critical habitat concurrent with the
listing (CNE et al. 2005, p. 1). We
considered the information in the
petition when we prepared the 2006
CNOR (71 FR 53756, September 12,
2006). Section 4(b)(3)(C) of the Act
requires that when we make a warranted
but precluded finding on a petition, we
are to treat such a petition as one that
is resubmitted on the date of such a
finding. We identified P. submutica as
a species for which we made a
continued warranted but precluded
finding on a resubmitted petition in the
Federal Register on December 6, 2007
(72 FR 69034), December 10, 2008 (73
FR 75176), and November 9, 2009 (74
FR 57804). We retained an LPN of 8 for
the species. In the 2008 CNOR, we
announced that we had not updated our
assessment for this species, as we were
developing a proposed listing rule (73
FR 75227). On June 23, 2010, we
proposed to list P. submutica as
threatened (75 FR 35721). In the
proposed rule, we found that critical
habitat for the species was prudent, but
not determinable at that time. A
proposed rule to designate critical
habitat for this species is being
published concurrently with this final
rule.
Summary of Comments and
Recommendations
We requested written comments from
the public on the proposed listing of
Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica during
the comment period associated with the
publication of the proposed rule (75 FR
35721), which opened on June 23, 2010,
and closed on August 23, 2010. We did
not receive any requests for a public
hearing. We also contacted appropriate
Federal, State, and local agencies;
scientific organizations; and other
interested parties and invited them to
comment on the proposed rule during
this comment period.
During the comment period, we
received 13 comment letters addressing
the proposed rule. All substantive
information provided during the
comment period has either been
incorporated directly into this final
determination or is addressed below.
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Peer Review
In accordance with our peer review
policy published on July 1, 1994 (59 FR
34270), we solicited expert opinions
from three knowledgeable individuals
with scientific expertise that included
familiarity with the species, the habitats
in which the species occur, and
conservation biology principles. We
received responses from the three peer
reviewers.
We reviewed all comments received
from the peer reviewers for substantive
issues and new information regarding
the proposed listing of Ipomopsis
polyantha, Penstemon debilis, and
Phacelia submutica. The peer reviewers
concurred with our analysis and
conclusions, and provided additional
information, clarifications, and
suggestions to improve the final rule.
Peer reviewer comments are addressed
in the following summary and
incorporated into the final rule as
appropriate.
Peer Reviewer Comments
(1) Comment: One peer reviewer said
that population trends cannot be
identified from available data for
Penstemon debilis and Phacelia
submutica, but noted that annual
fluctuations in plant numbers for both
species make them vulnerable to
additional stressors such as habitat loss.
Another reviewer said that the lowest
total annual plant count for P.
submutica should be zero, because the
plants do not emerge at all during very
dry years. An agency commenter was
concerned that the zero counts might
reflect inadequate survey methods.
Our Response: The low and high
plant counts reported for Phacelia
submutica are simply a record of the
lowest and highest plant counts
recorded during blooming season
surveys at known occupied sites. Not all
occurrences are visited every year. Zero
counts are reported only when a site
was visited, not as a default. We report
the negative surveys to show that the
plants really do not emerge during some
years, and that the fluctuations in plant
numbers make it hard to measure the
population trend.
(2) Comment: One peer reviewer
indicated the correct name for the
sensitive species of blazing star
associated with Penstemon debilis is
Mentzelia rhizomata (Roan Cliffs
blazingstar), not Mentzelia argillosa
(Arapien blazingstar).
Our Response: We corrected the text
in this final rule accordingly. This is an
important distinction, because
Mentzelia rhizomata is a Bureau of Land
Management (BLM) sensitive species
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that will benefit from protection of P.
debilis habitat because it only grows on
the same layers of shale.
(3) Comment: One peer reviewer
stated that the extent and imminent
nature of energy development may not
have been ameliorated to the extent
suggested in the proposed rule. In 2010,
natural gas production in the range of
Phacelia submutica and Penstemon
debilis was the highest in Colorado, an
increase from the 2008 report that was
cited in the proposal.
Our Response: We have updated this
final rule with the natural gas
production reports provided by the
reviewer and the Colorado Oil and Gas
Conservation Commission (2010, pp. 1–
2).
(4) Comment: One peer reviewer
stated the potential impact of climate
change on Penstemon debilis may be
greater than indicated in the proposal,
because the species is restricted to only
one layer of shale; thus, it may be
impossible for this species to migrate to
a more suitable climate space if the
substrate it depends upon does not
exist. The peer reviewer indicated that
Camille Parmesan (2006, p. 649) has
authored a more comprehensive and
current review documenting species’
distributional shifts in response to
warming.
Our Response: We have incorporated
Parmesan’s findings into our analysis of
Factor E for Penstemon debilis.
However, the current data are not
reliable enough at the local level for us
to draw conclusions regarding the
imminence of climate change threats to
P. debilis or the other two species.
(5) Comment: One peer reviewer
suggested the potential impacts of
fugitive dust on Penstemon debilis are
overstated in the proposed rule. For at
least the viable population on public
land, the nature of the road is
prohibitive to vehicles moving at speeds
that could generate much dust. Phacelia
submutica, which is more exposed to
dust, should have an evaluation of dust
impacts because it occupies habitat in
the vicinity of roads that can better
accommodate heavy, fast moving traffic.
Additionally, Phacelia submutica
habitats are more likely to be in the
vicinity of well pads and pipelines than
Penstemon debilis, and thus inclusion
of an evaluation of the threat from dust
on this species is warranted.
Our Response: We consider dust
effects an impact that does not rise to
the level of a threat to Penstemon debilis
or Phacelia submutica, because we do
not have research results to assess its
effect. However, we have observed
heavy dust settling on at least three of
the Penstemon debilis occurrences from
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heavy equipment and truck traffic
(Ewing 2009a, p. 3). Most Phacelia
submutica occurrences are not close to
dust-producing roads, but Service
biologists have observed dust sources
along a pipeline construction route near
Phacelia submutica occurrences.
(6) Comment: One peer reviewer
stated the proposed listing rule fails to
include pollinator information for
Phacelia submutica and the potential
for disruption of pollinator-plant
interactions due to climate variations.
Our Response: The pollination
mechanism for Phacelia submutica
remains unknown at this time. Based on
the size and shape of the flowers and
lack of insects observed on the flowers,
we expect that P. submutica is selfpollinated. We have initiated a
pollination study for this species, but
the results are not yet available. If the
species did depend on pollinators for
reproduction, then climate change could
disrupt this relationship because the
plants are receptive for a very short
time. Pollination could fail to occur if
the weather factors allowing the
pollinating insects to emerge were not
synchronized with plant receptivity.
Because we have no data to indicate that
pollinators are required, we do not
assess the effects of climate variations
on pollinator-plant interactions.
(7) Comment: One peer reviewer
indicated that critical habitat should be
determined for these three species based
on the information available at this
time. Given the level of threats and the
narrow distribution of all three species,
it is essential to provide the protection
of designated critical habitat as soon as
possible.
Our Response: We are proposing to
designate critical habitat for the three
species concurrently with this final rule.
That proposal is published elsewhere in
today’s Federal Register. Comments on
the proposal will be accepted following
publication.
(8) Comment: Peer reviewers and
commenters pointed out an error on
page 35733 of the proposed listing rule,
where the projected average temperature
warming per decade was correctly cited
as 0.2 °C, but the equivalent was
incorrectly shown as 32.4 °F.
Our Response: For the next 2 decades,
a warming of about 0.36 °F (0.2 °C) per
decade is projected. By the end of the
21st century, average global
temperatures are expected to increase
1.08 to 7.2 °F (0.6 to 4 °C)
(Intergovernmental Panel on Climate
Change (IPCC) 2007, p. 45). We
corrected the text in this final rule
accordingly.
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Comments From the State of Colorado
Section 4(i) of the Act states, ‘‘the
Secretary shall submit to the State
agency a written justification for his
failure to adopt regulations consistent
with the agency’s comments or
petition.’’ Comments received from the
State regarding the proposal to list
Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica are
addressed below. The Colorado Natural
Areas Program (CNAP) is the State
agency within Colorado State Parks that
works to cooperatively monitor and
protect Colorado’s most significant
natural features, including rare plants.
Penstemon debilis
(9) Comment: The CNAP is concerned
that listing Penstemon debilis will
discourage future voluntary protections
by the oil and gas industry. The CNAP
stated in its letter that Oxy USA, Inc.
(Oxy), has implemented voluntary best
management practices to avoid impacts
and reduce threats to the species, and
they have supported 3 years of
monitoring to document the status of
the species on their land. The CNAP
stated that although monitoring results
at Mount (Mt.) Callahan and Mt.
Callahan Saddle Natural Areas show a
statistically insignificant downward
trend in number of plant stems per plot,
this trend may be a natural variation in
population size or caused by climatic or
other environmental factors, not by any
effects from the gas well construction.
No impacts to the P. debilis individuals
were observed that may be related to
natural gas development in the Natural
Areas, and the buffers instituted are
believed to be adequate to protect the
populations. The CNAP will continue to
work with Oxy to track the trends of this
species. Monitoring will be done with
care to minimize negative impacts from
trampling of individual plants by people
collecting the data.
Our Response: The Service
acknowledges that Oxy has
implemented voluntary best
management practices to protect two of
the Penstemon debilis occurrences on
their private land. Oxy and other energy
companies are aware that their
compliance with conservation measures
recommended by the Service is entirely
voluntary. We believe that this level of
protection, while voluntary and nonbinding, minimizes the threats to the
species to an extent that we can list it
as threatened, rather than endangered.
We also must consider the cumulative
threats to the species as a whole
throughout its entire limited range in
making our listing decision. Despite the
positive conservation being
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implemented by Oxy, we determined
that the species still meets the definition
of a threatened species because of
cumulative effects of a variety of threats,
many not under the control of Oxy, and
the threats present in the remainder of
the species’ range.
Phacelia submutica
(10) Comment: The CNAP believes
that the greatest threat to Phacelia
submutica is oil and gas development
that may be allowed within occupied
habitat under current Federal
regulations, because some surveys in
potential habitat may not indicate the
presence of this ephemeral and
inconsistent species. Because this
species may not emerge on an annual
basis, that makes potential surveys for it
very challenging, and surveys could
result in the unintentional leasing and
development of occupied habitat.
Our Response: Our threats analysis
incorporates and supports CNAP’s
statement regarding the primary threats
to Phacelia submutica.
Federal Agency Comments
Penstemon debilis
(11) Comment: In response to our
description in the proposed rule of
impacts that resulted from inadequate
regulation, the BLM pointed out that the
Anvil Points Mine reclamation was a
Superfund project that was not subject
to the Act, and that section 7
consultation was not required for the
communication site access because the
species was only a candidate for listing.
Of the 88 plants at the reclamation site
that were transplanted, covered, or
fenced, BLM reported 71 survivors at
the end of the 2009 growing season.
Our Response: The BLM avoided and
minimized impacts from the
reclamation project voluntarily, with
input from the Service that was
comparable to a section 7 consultation.
However, plants were destroyed, habitat
was modified, and the ongoing issue of
impacts due to communication site
access remains unresolved. We believe
that listing as a threatened species will
provide more support for agency efforts
to protect the species.
Phacelia submutica
(12) Comment: The U.S. Forest
Service (USFS) feels that critical habitat
should not be designated for Phacelia
submutica at this time because we do
not have enough information about its
specific soil requirements, seed bank,
reproductive biology, or minimum
population size; and that new
populations being discovered each year
are leading to new concepts of the
species’ distribution and requirements.
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Our Response: Designation of critical
habitat for the three species is proposed
concurrently in a separate rule in this
edition of the Federal Register. The
criteria for critical habitat were
evaluated using the best scientific and
commercial data available. Surveys in
2009–2010 increased the known sites
and numbers of plants, but did not
change the habitat description or extend
the range boundaries. We believe that
Phacelia submutica has a large enough
range, enough populations, and enough
individuals that the occupied habitat
alone, if protected from threats, would
be adequate for the future survival and
recovery of the species. We recognize
that critical habitat designated at a
particular point in time may not include
all of the habitat areas that we may later
determine are necessary for the recovery
of the species. A critical habitat
designation does not signal that habitat
outside the designated area is
unimportant or may not be required for
recovery of the species.
which may require special management
considerations or protection; and (2)
Specific areas outside the geographical
area occupied by the species at the time
it is listed, upon a determination that
such areas are essential for the
conservation of the species. All known
occurrences are evaluated, and must
meet the criteria to be included in
proposed critical habitat.
Public Comments
(13) Comment: Support for listing the
three plants was received from the
Colorado Natural Heritage Program
(CNHP), seven other non-profit
environmental organizations in
Colorado, and one local resident. Some
of these commenters also believe that
the species proposed for listing as
threatened should not be subject to a
4(d) rule, which is a special regulation
that can provide greater flexibility by
allowing actions prohibited under
section 9(a)(1) of the Act for species
listed as threatened.
Our Response: We believe that the
general prohibitions for threatened
plants at 50 CFR 17.71 are appropriate
for these two plant species. As a result,
we did not develop a 4(d) rule for
Penstemon debilis or Phacelia
submutica, the two species we are
listing as threatened.
(14) Comment: Several environmental
groups commented that critical habitat
is both prudent and determinable for all
three species, and it should include all
known occurrences of each species,
including historical and recently
extirpated and nonviable, as well as
potential habitat.
Our Response: We are proposing
critical habitat for each of the three
species concurrently with this final
listing rule. Critical habitat is defined in
section 3 of the Act as: (1) The specific
areas within the geographical area
occupied by the species, at the time it
is listed in accordance with the Act, on
which are found those physical or
biological features that are essential to
the conservation of the species, and
Summary of Changes From Proposed
Rule
No substantial changes have been
made in the threats analysis or
determinations for the three species.
Field surveys in 2010 increased the
recorded number of plants for each
species, but did not expand their known
ranges or any decrease in the level of
threats.
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Penstemon debilis
(15) Comment: Andrea Wolfe shared
her unpublished results of genetic
research on Penstemon debilis in 2009,
which show that its genetic diversity is
very limited and each occurrence is
genetically separated from the others,
which indicates inbreeding depression.
Our Response: We appreciate
receiving these results, which indicate
the limited ability of Penstemon debilis
to adapt to habitat or climate changes.
We included them in our assessment of
other natural factors affecting the
species, under Factor E.
Endangered Status for Ipomopsis
polyantha; Threatened Status for
Penstemon debilis and Phacelia
submutica
Background
It is our intent to discuss below only
those topics directly relevant to the
listing of Ipomopsis polyantha as
endangered, and Penstemon debilis and
Phacelia submutica as threatened, in
this section of the final rule. More
information on these species is available
in the June 23, 2010, proposed rule (75
FR 35721).
Species Information—Ipomopsis
polyantha
Taxonomy and Species Description
Ipomopsis polyantha is a rare plant
endemic to shale outcrops in and
around the Town of Pagosa Springs in
Archuleta County, Colorado. The
species is in the Polemoniaceae (phlox)
family and was originally described by
Rydberg (1904, p. 634) as Gilia
polyantha. Two varieties, G. polyantha
var. brachysiphon and G. polyantha var.
whitingii, were recognized by Kearney
and Peebles (1943, p. 59). Grant (1956,
p. 353) moved the species into the genus
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Ipomopsis. Currently available
information indicates that I. polyantha
is a distinct species (Porter and Johnson
2000, p. 76; Porter et al. 2010, pp. 195,
196, 199). It is treated as such in the
PLANTS database (U.S. Department of
Agriculture, Natural Resource
Conservation Service (NRCS) 2003), and
in the Integrated Taxonomic
Information System (2001). Reports of
this species occurring in Arizona and
New Mexico by the PLANTS National
Database and State floras actually
pertain to the two species that were
formerly treated as varieties of
Ipomopsis polyantha (Anderson 2004,
pp. 11, 15).
The CNHP ranks Ipomopsis polyantha
as critically imperiled globally (G1) and
in the State of Colorado (S1) (CNHP
2010b, pp. 1–5). The Nature
Conservancy (TNC) and CNHP also
developed a scorecard that ranks I.
polyantha among the most threatened
species in the State based on number of
plants, quality of the plants and habitat,
threats, and adequacy of protection
(CNHP and TNC 2008, p. 102).
Ipomopsis polyantha is an herbaceous
biennial 12 to 24 inches (in) (30 to 60
centimeters (cm)) tall, branched from
near the base above the basal rosette of
leaves. Deeply divided leaves with
linear segments are scattered up the
stem. Stems and flower clusters are
covered with glandular hairs. Flower
clusters are along the stem in the axils
of the leaves as well as at the top of the
stem. The white flowers are 0.4 in (1
cm) long, with short corolla tubes 0.18
to 0.26 in (0.45 to 0.65 cm) long, and
flaring corolla lobes flecked with purple
dots (Anderson 1988, p. 3). These dots
are often so dense that they give the
flower a pinkish or purplish hue. The
stamens extend noticeably beyond the
flower tube, and the pollen is blue
(Grant 1956, p. 353), changing to yellow
as it matures (Collins 1995, p. 34). Seeds
form a mucilaginous (secreting sticky
mucous) coat after they are wet. Seeds
germinate much faster in Mancos Shale
soil than in potting soil (Collins 1995,
p. 72). Mature seeds germinate to form
rosettes that produce flowering stalks
during the next growing season, or they
may persist as rosettes for a year or more
until conditions are right for flowering.
Plants produce abundant fruits and
seeds, but have no known mechanism
for long-distance dispersal (Collins
1995, pp. 111–112). After seeds are
mature, the plants dry up and die. We
do not know how long the seeds remain
viable.
Pollination by bees is the most
common means of reproduction for
Ipomopsis polyantha, and the primary
pollinators are the honey bee (Apis
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mellifera), metallic green bee
(Augochlorella spp.), bumble bee
(Bombus spp.), and digger bee
(Anthophora spp.) (Collins 1995, pp.
71–72).
Ipomopsis polyantha is limited to
Pagosa-Winifred soils derived from
Mancos Shale. The soil pH is nearly
neutral to slightly alkaline (6.6 to 8.4).
The elevation range is 6,750 to 7,775
feet (ft) (2,050 to 2,370 meters (m))
(Service 2011c, p. 1). Plants occur in
discontinuous colonies as a pioneer
species on open shale or as a climax
species along the edge of Pinus
ponderosa (Ponderosa pine), mixed P.
ponderosa and Juniperus scopulorum
(Rocky mountain juniper), or Juniperus.
osteosperma (Utah juniper) and Quercus
gambellii (Gambel oak) forested areas. In
1988, Anderson (p. 7) reported finding
the highest densities under P.
ponderosa forests with montane
grassland understory. Now the species
is found mostly on sites that are
infrequently disturbed by grazing, such
as road right-of-ways (ROWs) that are
fenced from grazing (as opposed to open
range), lightly grazed pastures, and
undeveloped lots (Anderson 2004, p.
20).
The two known occurrences of
Ipomopsis polyantha are within about
13 miles (mi) (21 kilometers (km)) of
each other, and collectively occupy
about 388.4 acres (ac) (157.1 hectares
(ha)) of habitat within a range that
includes about 6.5 square mi (16.8
square km). The Pagosa Springs
occurrence is southeast of the Town of
Pagosa Springs along both sides of U.S.
84. Occupied habitat extends southward
on the highway ROW for 3 mi (4.8 km)
from the intersection with U.S. 160, and
on private lands on both sides of the
highway. The Dyke occurrence is about
10 mi (16 km) west of Pagosa Springs
along U.S. Highway 160. It includes 0.5
mi (0.8 km) of highway ROW on both
sides of U.S. 160, adjacent private land,
and a BLM parcel. Species occurrences
are further described in the June 23,
2010, proposed rule to list the species
(75 FR 35721). Table 1 summarizes land
ownership and results of the most
recent plant counts reported within the
two I. polyantha occurrences.
TABLE 1—OCCUPIED HABITAT FOR Ipomopsis polyantha BY LANDOWNERSHIP (ACRES (AC) (HECTARES (HA))
[Lyon 2006a; CNAP 2007; CNAP 2008, pp. 1–5; CNHP 2008a; CNHP 2010a, pp. 1–8; Service 2011a, p. 2; Service 2011b, p. 1]
ac
(ha)
Land ownership
Pagosa Springs including Mill Creek ........
State ROW ...............................................
County ROW ............................................
Town of Pagosa Springs ..........................
Private ......................................................
27.6 (11.2)
5.5 (2.2)
7.5 (3.0)
301.7 (122.1)
3,029
469
126
158,326
3,083
403
15
174,989
Subtotals ............................................
...................................................................
342.3 (138.5)
161,950
178,490
Dyke ..........................................................
State ROW ...............................................
BLM ..........................................................
Private ......................................................
2.3 (0.9)
9.9 (4.0)
33.9 (13.7)
19
88
163
102
164
275
Subtotals ............................................
...................................................................
46.1 (18.6)
270
541
Totals ..........................................
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Occurrence
...................................................................
388.4 (157.1)
162,220
179,031
Approximately 2.5 percent of the
occupied habitat is on Federally
managed BLM land, 9.1 percent on State
and County highway ROWs, 86.4
percent on private lands, and 1.9
percent on Pagosa Springs town park
land and county land (Service 2011a, p.
2).
In 2004, the total estimate of
flowering plants throughout the entire
range of the species was 2,246 to 10,526
(Anderson 2004, p. 40). Plant surveys
from 2005 to 2007 documented dramatic
increases in the number of flowering
individuals and rosettes within the
Pagosa Springs occurrence at two sites
on private land and on the U.S. 84 ROW
(CNAP 2007, pp. 1–2). This increase
was primarily attributed to the plants
surveyed in 2005 and 2006 on a 3-ac
(1.2-ha) private land site in the Pagosa
Springs occurrence. The rapid
appearance of such a dense patch of
plants illustrates the species’ ability to
colonize barren Mancos Shale soil, and
demonstrates the reproductive success
of the species; however, the sites where
they grow are vulnerable to habitat
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Flowering
Rosettes
destruction. Currently, the total estimate
of flowering plants is 162,220 (see Table
1 above). Again, the increase from 2,426
flowering plants counted in 2004 was
largely due to the discovery of
previously undocumented plants during
new surveys on private lands. The trend
in the species’ status since 1988 is one
of fluctuating population size that is
typical of biennial species, combined
with the loss of several hundred plants
due to development (see Factor A
below).
overutilization for commercial,
recreational, scientific, or educational
purposes; (C) disease or predation; (D)
the inadequacy of existing regulatory
mechanisms; or (E) other natural or
manmade factors affecting its continued
existence. Listing actions may be
warranted based on any of the above
threat factors, singly or in combination.
Each of these factors is discussed below.
Summary of Factors Affecting
Ipomopsis polyantha
Ipomopsis polyantha is threatened
with destruction of plants and habitat
due to commercial, residential,
municipal, and agricultural property
development, and associated new utility
installations and access roads. We have
documented recent losses of habitat and
individuals within the Pagosa Springs
and Dyke occurrences of the species, as
described in more detail below.
Section 4 of the Act and its
implementing regulations (50 CFR 424)
set forth the procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. A species may be
determined to be an endangered or
threatened species due to one or more
of the five factors described in section
4(a)(1) of the Act: (A) The present or
threatened destruction, modification, or
curtailment of its habitat or range; (B)
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A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Land Use Changes
Primary land use within the range of
Ipomopsis polyantha has historically
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been livestock (horses or cattle) grazing,
with homes on parcels of 35 ac (14 ha)
or more. Several small businesses now
occur along U.S. 84 within the Pagosa
Springs occurrence. The intersection of
U.S. 160 and U.S. 84 is zoned by the
Town of Pagosa Springs for business,
and commercially zoned land is
currently available for development.
Archuleta County also is considering
sites in this area for new county
buildings. These current and potential
conversions of agricultural lands to
residential and commercial
development are incompatible with
conservation of I. polyantha in the long
term because the conversions cause
direct mortality and permanent loss of
habitat. Conversely, habitat modified by
grazing may be recovered by changes in
management.
Residential development is increasing
in Archuleta County. The population of
Archuleta County was 5,000 in 1990,
increasing to 12,430 in 2009 (U.S.
Census Bureau 2011). Prior to the
slowing down of the real estate market
over the past few years, projections for
new development in Archuleta County
were high. For example, all private land
across the entire range of Ipomopsis
polyantha is scheduled for development
in the Archuleta County and Town of
Pagosa Springs Community Plan (2000).
In this plan, all areas occupied by I.
polyantha on private land outside of the
Town limits are planned for low (35 ac
(14 ha)), medium (3 to 35 ac (1.2 to 14
ha)), or high (2 to 5 ac (0.81 to 2 ha))
density housing. The rate of current and
proposed development is the most
significant threat to the species, because
development planned for the next 5 to
10 years will likely impact 86 percent of
the species’ habitat. This rate of land
conversion puts the species at risk of
extinction.
Private Development of 35 Acres (14
Hectares) or Less
Within the Pagosa Springs
occurrence, a residential and
agricultural development of about a
dozen 35-ac (14-ha) parcels was built
prior to 2005 on occupied habitat east
of U.S. 84 (Archuleta County Assessor
2008, p. 1). In 2005, when most
residences were new, about 782
flowering plants were counted in
meadows and along the fences and
access roads (Lyon 2005, pp. 1–2). By
2008, an increased number of horses
were pastured in the meadows,
roadsides and driveways were graded or
widened, and few plants or rosettes
could be found as a result (Mayo 2008b,
p. 2). This information indicates that
Ipomopsis polyantha plants are
vulnerable to grazing effects and road
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improvements, and habitat can be
modified to exclude plants in as few as
3 years. We do not know exactly what
level of grazing is sufficient to eliminate
the I. polyantha plants in a pasture. In
2006, at another location along U.S. 84,
a private landowner mowed several
hundred feet of occupied habitat on the
highway ROW (Lyon 2006a, p. 1). No
plants or rosettes were found at this site
from 2006 to 2008, indicating that
mowing destroys plants and halts
reproduction. In 2005, dense patches of
flowering plants were noted, from
across the fence, in a privately owned
meadow along U.S. 84. In 2007, a new
home was built, and the meadow was
mowed; no plants could be seen at the
same site in 2008 (Mayo 2008b, p. 2),
again indicating that mowing destroys
flowering plants and inhibits
reproduction, because the seeds cannot
mature and grow into rosettes. We do
not know how long the seeds remain
viable in the soil.
Private and County Development of
Large Parcels
In 2008, the Pagosa Springs Town
Council approved annexation of the 96ac (39-ha) private development called
Blue Sky Village into the Town (Aragon
2008a, pp. 1–2). The proposed
development plan was for a mixed
commercial and high- to low-density
residential village (Hudson 2008, p. 1).
The 96-ac (39-ha) parcel is adjacent to
the highest density of Ipomopsis
polyantha plants, and includes about
2,562 ft (781 m) of habitat on U.S. 84
frontage at the center of the species’
distribution (Archuleta County Assessor
2008, p. 1). Plants have been observed
on the property from over the fence, but
not counted. Occupied habitat also
borders the southern edge of the
property.
In 2010, the Blue Sky Village property
went into foreclosure. The County
announced that it will acquire the
property. Possible uses of the land
include county buildings, sports fields,
and the sale of commercial lots along
the highway (Hudson 2010, p. 1).
Development of the Blue Sky Village/
County property would significantly
reduce the amount of habitat within the
species’ range. Location of the
development between the highest
density of plants and the rest of the
Pagosa Springs occurrence on the east
side of U.S. 84 would further fragment
the habitat that has already been
impacted by commercial, residential,
and agricultural land uses.
Another private development that
includes 47 ac (19 ha) of occupied
habitat and about 1 mi (1.6 km) of
frontage along the west side of U.S. 84,
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is being considered for annexation and
development (Aragon 2008a, p. 2;
Archuleta County Assessor 2008, p. 1;
Hudson 2010, p. 1). Preliminary plans
show home sites and open space on the
47 ac (19 ha) of currently occupied plant
habitat.
The above two development
proposals would cover about 42 percent
of the habitat within the Pagosa Springs
occurrence, which is the larger of the
two occurrences and is essential to the
species’ continued existence. Plants and
habitat along U.S. 84 ROW are likely to
be disturbed or destroyed by
construction of new access roads, utility
installations, and acceleration and
deceleration lanes built to accommodate
the proposed developments. The pace of
development around Pagosa Springs
fluctuates with the economy, but given
the direction in the County plan and the
projected growth rates for the County
and the Town of Pagosa Springs, it is
highly likely that further development
will occur along U.S. 84 within 5 to 10
years.
A third large parcel of 1,362 ac (551
ha) proposed for development, plus
2,819 ft (859 m) of U.S. 84 frontage, is
another annexation to the Town of
Pagosa Springs being considered within
the range of Ipomopsis polyantha. The
proposed development, called Blue Sky
Ranch, would include single and multifamily residential housing, a hotel and
conference center, a golf course with
clubhouse, and an equestrian center
with riding trails and a multi-use arena
(Aragon 2008b, p. 2). The status of the
proposed development is unknown at
this time, because it depends on the real
estate market. This area has not been
surveyed for plants, and is not included
in the total occupied habitat.
Utilities Installations and Maintenance
Utilities installations and
construction activities that are necessary
for development can eliminate habitat
and destroy Ipomopsis polyantha
plants. During 2005 and 2006, a sewer
line installation on the U.S. 84 ROW
resulted in the loss of about 498 plants
and 541 rosettes and the modification of
about 1,473 ft (449 m) of roadside
habitat (Mayo 2008c, p. 8). The
Colorado Department of Transportation
(CDOT) and Archuleta County
consulted with the Service, and agreed
on avoidance measures for this project,
but contractors failed to follow the
protocol. Where avoidance of plants and
habitat was specified, topsoil, plants,
and rosettes were scraped away on the
bank; where native plant seeding was
specified, nonnative grasses were
seeded; and where straw was
prohibited, a thick layer of straw was
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applied (Mayo 2008c, pp. 1–4; Peterson
2006, pp. 1–3). As a result, in 2008, the
remaining 8 flowering plants and 5
rosettes at this site were found in one
spot, near plants on an adjacent
property not disturbed by the sewer line
project (Mayo 2008c, p. 8). In 2010, the
combined number of flowering plants
and rosettes at the site was 167. This
incident demonstrates that I. polyantha
cannot quickly recover from soil
disturbance.
Although I. polyantha can colonize
unvegetated Mancos Shale soil near a
seed source, the number of flowering
plants that appear in subsequent years
depends on seed production and the
survival of rosettes that are not
outcompeted by other species or
destroyed during ground disturbance.
Power line maintenance was completed
within occupied habitat in the Pagosa
Springs occurrence in 2007. As a result
of careful planning, there was negligible
damage to adult plants. However, 278
rosettes were transplanted, but did not
survive to reproduce for unknown
reasons. We conclude that the species is
highly vulnerable to ground disturbance
during development because seedlings
and rosettes are destroyed and
transplanting is not known to be
successful.
Highway Right of Ways
The Archuleta County and Town of
Pagosa Springs revised 2004 Trails Plan
(2004, p. 18) calls for an 8-ft (2.4-m)
wide, 2.5-mi (4-km) long, paved bike
path on the highway ROW from U.S.
160 south along U.S. 84 in occupied
Ipomopsis polyantha habitat. This
route, prioritized for completion as soon
as funding is available, would eliminate
about 38 percent of the total occupied
habitat on the highway ROWs and 4
percent of the total occupied habitat for
the species (see Table 1 above). Another
planned paved bike trail, parallel to U.S.
160 and through the Dyke occurrence of
I. polyantha, is on the low priority list
in the Trails Plan (Archuleta County
and Town of Pagosa Springs 2004, p.
28). Development of this bike trail
would eliminate the portion of the Dyke
occurrence located on the south side of
the highway where the trail would be
located, covering about 3 percent of the
total highway ROW habitat.
The distribution of Ipomopsis
polyantha within highway ROWs makes
this species susceptible to threats
associated with highway activities and
maintenance. Exotic grasses planted by
CDOT along roadsides dominate the
ROW between pavement and ditch,
limiting most I. polyantha plants to the
ROW bank between ditch and fence.
This limitation to the species’ habitat
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along roadsides is significant because so
little habitat exists elsewhere for the
species. I. polyantha plants growing
within the highway ROW along U.S. 84
in 2004 were killed when the thistles
growing among them were treated with
herbicide (Anderson 2004, p. 36). Since
that time, Archuleta County has
discontinued broadcast herbicide use
and mowing on ROWs within the
species’ range. However, the planted
exotic grasses continue to limit the
species’ habitat.
Highway ROWs provide about 9
percent of the occupied habitat for
Ipomopsis polyantha. All highway ROW
habitat is at risk of disturbance by
construction of new access roads or
acceleration lanes, bike paths, and
utilities installation or maintenance.
Such construction results in direct loss
of I. polyantha individuals or reduced
suitability of its habitat by altering the
soil characteristics (Anderson 2004, p.
36).
Summary of Factor A
We determined that the present and
threatened destruction, modification,
and fragmentation of Ipomopsis
polyantha habitat from commercial,
municipal, agricultural, and residential
development, associated new utility
installations, construction of new access
roads and bike paths, competition from
introduced roadside grasses, and other
impacts to highway ROWs are
significant and imminent threats to the
species throughout its range. At this
time, the species persists primarily on
private lands (about 86 percent) and
highway ROWs (about 9 percent). Based
on the rate of current and proposed
development over the entire range of the
species, we estimate that 95 percent of
the species’ habitat could be modified or
destroyed within 5 to 10 years. The
plants would then be relegated to 10 ac
(4 ha) of BLM land; 7.5 ac (3 ha) of
Town park land; small, fragmented
portions of highway ROWs; and a few,
small, lightly used, private yards and
pastures, thus putting the species in
danger of extinction.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Activities resulting in overutilization
of Ipomopsis polyantha plants for
commercial, recreational, scientific, or
educational purposes are not known to
exist. Therefore, we do not consider
overutilization for commercial,
recreational, scientific, or educational
purposes to be a threat to the species
now or in the foreseeable future.
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C. Disease or Predation
Disease
Disease is not known to affect
Ipomopsis polyantha. Therefore, we do
not consider disease to be a threat to the
species now or in the foreseeable future.
Predation
This species is threatened by
destruction of flowering plants, rosettes,
and seeds due to concentrated livestock
disturbance and some herbivory.
Observations of the ‘‘fence line effect’’—
healthy plants outside the fence and
impacted plants inside the fence—at
several locations on private land used
for cattle and horse grazing indicate that
Ipomopsis polyantha does not tolerate
intensive livestock grazing (Anderson
2004, p. 30). For example, grazing by
horses at a residential/agricultural
development within the Pagosa Springs
occurrence in 2005 resulted in few I.
polyantha plants 3 years later (Mayo
2008b, p. 2). Over-the-fence
observations from seven locations
(pastures) in 2009 found few or no
plants in the three heavily grazed
pastures and numerous plants in the
adjacent pastures with light or no
grazing (Glenne and Mayo 2010, pp. 1–
3). We do not know whether the
destruction of the plants was a result of
herbivory or trampling. I. polyantha is
not found in heavily grazed pastures,
but occurrences have been observed in
lightly grazed horse pastures and
abandoned pastures (CNAP 2007, p. 6).
Plants could possibly recolonize a
pasture if livestock numbers were
reduced sufficiently and the seed bank
was still viable, or if there was a seed
source nearby, such as on the ungrazed
side of a fence. Indications are that the
species may persist in areas with light
grazing, but the level of impact and the
threshold of species’ tolerance have not
been studied. Few plants persist in areas
of continual grazing (Collins 1995, pp.
107, 111, 112). We determined that
destruction of flowering plants, rosettes,
and seeds due to heavy livestock use is
a significant and ongoing threat to I.
polyantha now and in the foreseeable
future.
D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
Town and county zoning ordinances
have the potential to affect Ipomopsis
polyantha and its habitats. We know of
no town or county regulations that
provide for protection or conservation of
I. polyantha or its habitat. As discussed
under Factor A above, Archuleta County
road maintenance crews voluntarily
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refrain from mowing or broadcast
spraying ROWs within the range of
Ipomopsis polyantha; however, there is
no law, regulation, or policy requiring
them to do so. New annexation of 2,018
ac (817 ha) into the Town of Pagosa
Springs will change zoning from 35-ac
(14-ha) residential and agricultural
parcels to commercial and small lot
residential, with anticipated adverse
impacts to the Pagosa Springs
occurrence of I. polyantha, as described
under Factor A above. Decisions
regarding annexations into the town and
changes in allowable subdividing of
parcels in the county are currently being
made to encourage growth that will
boost the local economy. Provisions for
avoidance or minimization of
disturbance to habitat for the plants are
not included in these decisions or plans.
mstockstill on DSK4VPTVN1PROD with RULES2
State Laws and Regulations
No State regulations protect rare plant
species in Colorado. Ipomopsis
polyantha is classified by CNHP as a G1
and S1 species, which means it is
critically imperiled across its entire
range and within the State of Colorado
(CNHP 2010b, pp. 1–5). The CDOT has
drafted best management practices for
ROWs within I. polyantha habitat in
collaboration with the Service (Peterson
2008, p. 1), but the agreement has not
been finalized. In 2006, voluntary
measures to minimize impacts to plants
from a sewer line installation along U.S.
84 were recommended by CDOT and
supervised by the county, but not
implemented by the contractors, as
described under Factor A (Mayo 2008c,
pp. 1–4; Peterson 2006, pp. 1–3).
Federal Laws and Regulations
Ipomopsis polyantha is on the
sensitive species lists for the USFS
(2006, pp. 5, 6, 13, 15–20; USFS 2009,
p. 6) and the BLM (2000, p. 3; 2008b,
p. 47). Occupied habitat has not been
found on USFS land, but there is nearby
habitat that appears to be suitable, so
the species is included in project
clearance surveys on the forest. In 2006,
we estimated that the Dyke occurrence
extended onto 20 ac (8 ha) of BLM land
(Lyon 2007b, pp. 3, 12, 13); 88 plants
and 164 rosettes were found there in
2007 (CNAP 2007, p. 2). In 2010, we
revised the estimated occupied BLM
habitat to 9.9 ac (4.0 ha) (Service 2011a,
p. 2). This BLM parcel was withdrawn
from a proposed land exchange so that
the plant habitat would remain under
Federal management (Brinton 2009,
pers. comm.; Lyon 2007b, p. 3). We
believe that BLM adequately protects
Ipomopsis polyantha on its lands
pursuant to the Federal statutes and
regulations that guide Federal land
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management. However, so little of the
species’ habitat occurs on BLM lands
that the BLM can do little to influence
the overall status of the species.
Summary of Factor D
We reviewed the suite of existing
regulatory mechanisms that could
potentially offer some protection to
Ipomopsis polyantha, including the
Federal Land Policy and Management
Act (FLPMA)(43 U.S.C. 1701 et seq.),
and State and local laws and
determined that these existing
regulatory mechanisms are inadequate
to address the primary threats to the
species. Ninety-seven percent of the
known range of the species is on State,
Town, and private lands, affording the
species little to no protection on these
lands. Federal statutes and regulations
governing natural resource protection
apply only to 2.5 percent of the
occupied habitat and therefore can do
little to influence the overall status of
the species. The State of Colorado offers
no regulatory protection to plants,
which means that protection falls upon
local County and Town ordinances. The
planning regulations governing growth
in Archuleta County and the Town of
Pagosa Springs do not contain any
requirements to protect rare plants,
including I. polyantha, when siting new
growth and development. In fact, the
current county planning regulations
contribute to the risk of extinction for
the species by facilitating development
in the last remaining habitat occupied
by the species. Therefore, we
determined that existing regulatory
mechanisms do not adequately address
the primary threats to the species.
E. Other Natural or Manmade Factors
Affecting the Species’ Continued
Existence
Habitat and Distribution
The adaptation of Ipomopsis
polyantha to Pagosa-Winifred soils
derived from Mancos Shale limits it to
about 6.5 square mi (16.8 square km)
within a 13-mi (21-km) range of
fragmented habitat on outcrops of
Mancos Shale. The species has specific
physiological requirements for
germination and growth that may
prevent its spread to other locations
(Anderson 2004, pp. 23–24). In
greenhouse trials, seeds will germinate
and grow on other soils, but they grow
much faster on Mancos Shale soils
(Collins 1995, p. 114). Faster growth
may give I. polyantha a competitive
advantage on relatively barren Mancos
shale that it lacks on other soils, where
its smaller seedlings have more
competition from other plants for
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nutrients and water. The species
produces more seed when it is crosspollinated (Anderson 2004, p. 23);
therefore, existing and foreseeable
fragmentation of habitat may cause gene
flow to be obstructed. Pollinatormediated pollen dispersal is typically
limited to the foraging distances of
pollinators, and no bee species is
expected to travel more than 1 mi (1.6
km) to forage (Tepedino 2009, p. 11).
Thus, it is likely that the Dyke
occurrence, of about 270 plants and 541
rosettes, is genetically isolated from the
Pagosa Springs occurrence 13 miles (21
kilometers) away. Spatially isolated
plant populations are at higher risk of
extinction due to inbreeding depression,
loss of genetic heterogeneity, and
reduced dispersal rates (Silvertown and
Charlesworth 2001, p. 185).
Transplanting
Rosettes in the path of power pole
replacements were transplanted to
suitable habitat in the town park in
2007. The 278 transplants survived the
winter and produced about 27 flowering
plants. However, no surviving rosettes
could be relocated in the fall of 2007,
and no evidence of trampling or habitat
destruction was found (Coe 2007, pp. 2–
3). Another attempt at transplanting
rosettes, to save them from destruction
during utility installations in 2005, was
not effective in producing new rosettes
in the third year (Brinton 2007, pers.
comm.). There was no evidence of
trampling or habitat destruction with
these transplants. Unless effective
methods are developed, most plants that
cannot be avoided during utility
installations and construction activities
are unlikely to survive and reproduce.
Whether the species can survive
translocation under other circumstances
remains uncertain, but at this time we
consider transplantation an ineffective
method of mitigating the impacts of
development. For this reason, we
conclude that the species is highly
vulnerable to development because
populations cannot be successfully
moved out of the way.
Fluctuating Population Size
Ipomopsis polyantha shows great
differences in plant numbers from year
to year, probably because the plants are
biennial and grow from seed. This trait
makes them more vulnerable than
perennials to changes in environment,
including timing and amount of
moisture and length of time since
disturbance. With increased time after
disturbance, competition from both
native and nonnative plants increases
(CNAP 2008a, p. 4). As a biennial
species, I. polyantha also may be
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vulnerable to prolonged drought. During
drought years, seeds may not germinate
and plants may remain as rosettes
without flowering or producing a new
crop of seeds.
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Climate Change
Habitat changes as a result of climate
change could potentially impact
Ipomopsis polyantha. Localized
projections indicate the southwest
United States may experience the
greatest temperature increase of any area
in the lower 48 States (IPCC 2007, p.
30). A 10 to 30 percent decrease in
precipitation in mid-latitude western
North America is projected by the year
2050, based on an ensemble of 12
climate models (Milly et al. 2005, p. 1).
Climate modeling at this time has not
been refined to the level that we can
predict the amount of temperature and
precipitation change within the limited
range of I. polyantha. Therefore, this
analysis is speculative based on the data
available at this time. When plant
populations are impacted by reduced
reproduction during drought years, they
may require several years to recover.
Climate change may exacerbate the
frequency and intensity of droughts in
this area and result in reduced species’
viability as the dry years become more
common. As described above, I.
polyantha is sensitive to the timing and
amount of moisture due to its biennial
life history. Thus, if climate change
results in local drying, the species could
experience a reduction in its
reproductive output.
Recent analyses of long-term data sets
show accelerating rates of climate
change over the past 2 or 3 decades,
indicating that the extension of species’
geographic range boundaries towards
the poles or to higher elevations by
progressive establishment of new local
occurrences will become increasingly
apparent in the short term (Hughes
2000, p. 60). The limited geographic
range of the Mancos Shale substrate that
underlies the entire Ipomopsis
polyantha habitat likely limits the
ability of the species to adapt by shifting
occurrences in response to climatic
conditions.
Summary of Factor E
We determined that the natural and
human-caused factors of specific soil
and germination requirements,
fragmented habitat, effects of drought
and climate change, and lack of proven
methods for propagation and
reintroduction present an imminent and
moderate degree of threat to Ipomopsis
polyantha across the entire range of the
species. These factors make the species
highly vulnerable to the development
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threats described under Factor A, and it
is highly unlikely that the species could
respond to these threats by extending its
range.
Cumulative Impacts
Some of the threats discussed in this
finding could work in concert with one
another to cumulatively create
situations that potentially impact
Ipomopsis polyantha beyond the scope
of each individual threat. For example,
as discussed under Factor A,
destruction and modification of habitat
by clearing the ground, mowing and
weed spraying, and concentrated
livestock grazing could reduce the
number of available pollinators for the
plants by removing other species of
blooming plants that attract pollinators
and by destroying the ground-nesting
habitat needed by bees. A reduction in
bee pollinators could cause I. polyantha
to produce fewer seeds. Such
cumulative impacts from developmentrelated activities are likely to impact the
species, given the ubiquity of
development within the habitat.
We have not identified other likely
scenarios where the threats discussed in
the five factors above have potential to
interact synergistically to produce
threats to Ipomopsis polyantha beyond
those which we have analyzed.
Summary of Factors
The Pagosa Springs occurrence of
Ipomopsis polyantha totals
approximately 342 ac (138 ha) of
Ipomopsis polyantha habitat, including
3 mi (4.8 km) of highway ROW and the
private properties on either side of the
highway. The smaller Dyke occurrence
of about 46 ac (19 ha) includes highway
ROWs, private land, and 10 ac (4 ha) of
BLM land. Destruction of plants, when
combined with the modification and
fragmentation of habitat within this
small range, results in a substantial loss
to the viability of the species. Both
known occurrences face ongoing, new,
and foreseeable threats, including
commercial, residential, agricultural,
and municipal development; associated
road and utility improvements and
maintenance; heavy livestock use;
inadequacy of existing regulatory
mechanisms to address the primary
threats to the species; fragmented
habitat; and prolonged drought
conditions. The magnitude of threat for
I. polyantha is high due to the direct
overlap of ongoing and planned land
development on 95 percent of the
known habitat. The overall impact of
current and planned development is
likely to result in extensive disturbance
and destruction of the remaining habitat
within the foreseeable future of 5 to 10
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years, depending on economic growth
in the area, thus putting the species in
danger of extinction.
Species Information—Penstemon debilis
Description
Penstemon debilis is a rare plant,
endemic to oil shale outcrops on the
Roan Plateau escarpment in Garfield
County, Colorado. This species is
known by the common names Parachute
beardtongue and Parachute penstemon.
P. debilis is classified by the CNHP as
a G1 and S1 species, which means it is
critically imperiled across its entire
range and within the State of Colorado
(CNHP 2010b, pp. 6–10). Traditionally,
the genus Penstemon was included in
the Scrophulariaceae (figwort) family.
However, Penstemon is now considered
to be within the Plantaginaceae
(plantain) family due to recent research
using DNA sequences (Oxelman et al.
2005, p. 415). We recognize this
placement and make the appropriate
attribution in the amendments to 50
CFR 17.12(h) at the end of this
document. The text includes the family
name as Plantaginaceae.
Penstemon debilis was discovered in
1986, and was first described by O’Kane
and Anderson in 1987 (pp. 412–416). P.
debilis is a mat-forming perennial herb
with thick, succulent, bluish leaves,
each about 0.8 in. (2 cm) long and 0.4
in. (1 cm) wide. Plants produce shoots
that run along underground, forming
what appear as new plants at short
distances away. Individual P. debilis
plants are able to survive on the steep,
unstable, shale slopes by responding
with stem elongation as leaves are
buried by the shifting talus. Buried
stems progressively elongate down
slope from the initial point of rooting to
a surface sufficiently stable to allow the
development of a tuft of leaves and
flowers (O’Kane and Anderson 1987,
pp. 414–415). The funnel-shaped
flowers are white to pale lavender, and
bloom during June and July. P. debilis
plants produce a small number of seeds
that are dispersed by gravity. They
require cross pollination, and have
many different pollinators that vary
between occurrences (McMullen 1998,
p. 26). None of the pollinators are
specialists to P. debilis, nor are any of
them rare (McMullen 1998, p. 31).
Genetic diversity in all populations of
P. debilis surveyed is very limited and
there is little contact among the
populations, which indicates inbreeding
depression (Wolfe 2010, pers. comm.).
There is a close genetic relationship
between the two Mount Callahan
populations. The Anvil Points
populations are also clustered together,
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and the Mount Logan population is
intermediate between the other groups
(Wolfe 2010, pers. comm.).
Habitat
Penstemon debilis seems to be
adapted to natural physical disturbance
(McMullen 1998, p. 81). Many of the
characteristics that are most similar
among sites promote continual shifting
of the substrate: steep slopes, unstable
surface layers of broken shale rubble,
and no surface soil (McMullen 1998, p.
82). The plants grow on steep, oil shale
outcrop slopes of white shale talus at
8,000 to 9,000 ft (2,400 to 2,700 m) in
elevation on the southern escarpment of
the Roan Plateau above the Colorado
River and the town of Parachute,
Colorado. The Roan Plateau falls into
the geologic structural basin known as
the Piceance Basin. Average annual
precipitation at Parachute, Colorado, is
12.75 in (32.4 cm) (IDcide 2009, p. 1),
which is considered a high desert
climate. P. debilis is found only on the
Parachute Creek Member of the Green
River Formation. P. debilis is often
found growing with other species
endemic to the Green River formation,
including Mentzelia rhizomata (Roan
Cliffs blazingstar) (Reveal 2002, pp.763–
767), Astragalus lutosus (dragon
milkvetch), Festuca dasyclada (Utah
fescue), and Thalictrum heliophilum
(sun-loving meadowrue), as well as
several non-endemics (O’Kane &
Anderson 1987, p. 415).
Distribution
The historical range and distribution
for this species is unknown. All of the
currently known occurrences occupy
about 91.8 ac (37.2 ha) on the Green
River geologic formation in Garfield
County, Colorado. Although this
45063
formation is underground throughout
most of the Piceance Basin, it is exposed
on much of the southern face of the
Roan Plateau, to which the plant is
restricted. The total area of the plant’s
geographic range is about 2 mi (3 km)
wide and 17 mi (27 km) long. Six
occurrences of Penstemon debilis were
found between 1986 and 2005; two of
them are no longer viable (CNHP 2010a,
pp. 9–23). It is likely that unknown
occurrences exist, because many areas
are inaccessible to surveyors due to
cliff-side terrain or private land
ownership or both.
Occurrences
Penstemon debilis occurrences are
described in the proposed rule to list the
species (75 FR 35728–35729) and
summarized in Table 2.
TABLE 2—Penstemon debilis OCCURRENCES BY LANDOWNERSHIP (ACRES (AC) (HECTARES (HA))
[CNHP 2010a, pp. 9–23; Ewing 2008a; Ewing 2009a; DeYoung 2008a pers. comm.; DeYoung 2009b, pers. comm.; DeYoung 2009c, pers.
comm.; Service 2011a, p. 4]
Occurrence
Viability
Number of
plants
ac (ha)
Total plant
mortality*
Trend
Mt. Callahan Natural
Area.
Mt. Callahan Saddle
Natural Area.
Smith Gulch ..................
Anvil Points Mine ..........
Anvil Points Rim ............
Mt. Logan Mine .............
Excellent ......
2,200 ...........
32.7 (13.2) ..........................
None ...........
Good ...........
650 ..............
3.8 (1.5) ..............................
None ...........
Fair ..............
Good ...........
Poor ............
Fair ..............
Mt. Logan Road ............
Poor .............
50 ................
700 ..............
2 ..................
483 Private ..
50 BLM ........
3 ..................
13.4 (5.4) ............................
5.3 (2.1) ..............................
5.7 (2.3) ..............................
24.7 (10.1) Private .............
5.8 (2.3) BLM .....................
0.4 (0.2) ..............................
Unknown .....
20 ................
250 ..............
30 ................
.....................
7 ..................
Stable to slightly downward.
Stable to slightly downward.
.......................................
Small downward ...........
Nearly extirpated ...........
Small downward ...........
.......................................
Nearly extirpated ...........
Total .......................
.....................
4,138 ...........
91.8 (37.1) ..........................
307 ..............
Land
ownership
.......................................
Private.
Private.
BLM.
BLM.
BLM.
Private.
BLM.
BLM.
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* Total of all dead plants reported from all sources.
Two occurrences on BLM land, Anvil
Points Rim and Mt. Logan Road, have
lost 257 plants and are nearly
extirpated. Because these two
occurrences have only five plants
remaining and we do not expect them
to recover, we consider these
occurrences nonviable, and focus our
analysis of ongoing and foreseeable
threats on the four viable occurrences.
The occurrences on BLM land
represent about 19.4 percent of the total
plants counted and approximately 33.3
percent of the occupied habitat. A new
Smith Gulch location on BLM land has
been added to the Mt. Callahan Saddle
occurrence because it is on shale
deposited at the base of the cliffs
directly below the saddle (Graham
2009a, pp. 1–2). Oxy USA Inc. owns
land that contains 68.9 percent of the
total plants on 39.8 percent of the
occupied habitat, with agreements
directing management of lands under
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their control. The Oxy oil shale division
owns land with 11.6 percent of the
plants on 26.9 percent of the occupied
habitat, with no management
agreements.
Summary of Factors Affecting
Penstemon debilis
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Penstemon debilis habitat is
threatened by energy development and
associated impacts. Of the four known
viable occurrences (Mt. Callahan and
Mt. Callahan Saddle Natural Areas,
Anvil Points Mine, and Mt. Logan
Mine), all but the Anvil Points Mine
occurrence are on lands wholly or
partially owned by energy development
companies. All four viable occurrences
face ongoing or potential threats,
including oil and gas development, oil
shale extraction and mine reclamation,
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road construction and maintenance, and
vehicle access through occurrences.
Oil and Gas Development
The Mt. Callahan and Mt. Callahan
Saddle Natural Area occurrences, which
include approximately 68.9 percent of
the total known Penstemon debilis
plants on 39.7 percent of the occupied
habitat, occur on land owned by Oxy
USA Inc. (Oxy). These occurrences are
behind locked gates, making them
inaccessible to the public. Oxy has
developed two natural gas well drilling
pads within a 680–ac (275–ha) area that
includes both occurrences (Webb 2008,
p. 1). One pad is located 360 ft (110 m)
from the nearest known P. debilis
individual and 105 ft (32 m) uphill from
its habitat (Ewing 2008a, p. 2). The other
pad is located farther from the habitat,
where runoff will flow down the
opposite side of the ridge. Operation of
these wells could potentially impact P.
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debilis by dust generation, loss of
pollinator habitat, spills of produced
water or other drilling wastes, and
inadvertent trampling by employees and
contractors. Monitoring of the
occurrences, in connection to the energy
development, has resulted in trampling
of individual plants by people collecting
the data (Ewing 2009a, pp. 1–2).
To protect plants and habitat from
potential impacts, CNAP and Oxy have
agreed to best management practices
and conservation measures, to include
plant surveys, surface disturbance
buffers, designated travel routes,
handling of produced wastes, dust
abatement, a monitoring plan for the
plants, and weed management. Working
with Oxy, CNAP designated the areas of
Mt. Callahan and Mt. Callahan Saddle
as State Natural Areas (Kurzel 2008,
pers. comm.; CNAP 1987, pp. 1–7;
CNAP 2008a, pp. 1–7; Webb 2008, p. 1).
Through these designations, the
landowner has agreed to develop
natural gas pads in a way that will avoid
or minimize impacts to the P. debilis
occurrences (Ewing 2008a, pp. 1–2). The
agreements include conservation
measures such as storm water
management and a noxious weeds
management plan (CNAP 2008c, pp. 1–
4; CNAP 2008d, pp. 1–4). The CNAP has
been very successful in garnering
landowner participation in conservation
of rare species in Colorado. The plant
habitat on the natural areas appears
unmodified by the gas well pad activity.
Trampling of plants during monitoring
has been noted as a minor impact that
will be minimized in the future by
modifying the sampling methods.
Natural area agreements are voluntary
and can be terminated at any time by
either party with a 90-day written
notice. However, we believe that these
natural area agreements for P. debilis,
while voluntary and non-binding,
minimize the threats to the species to an
extent that we can list it as threatened,
rather than endangered.
The Smith Gulch location of an
estimated 50 plants was discovered on
BLM lands below the Mt. Callahan
occurrences at the base of the cliffs
during surveys for a proposed oil and
gas development project in June 2009
(Graham 2009a, p. 1). Two well pads,
and corresponding roads and pipelines,
were proposed for this area (Graham
2009a, p. 3; Graham 2009b, pers.
comm.). Following an environmental
assessment, two well pads were
permitted, to be located about 800 ft
(244 m) downslope from the plants. The
pads have not been built as of February
2011 (DeYoung 2011b, pers. comm.).
When development proceeds, we
anticipate no significant impacts to the
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plants unless they get washed down the
drainage into the gas well area, which
we cannot predict. Potential minor
impacts are loss of pollinator habitat,
dust impacts, or inadvertent trampling.
Oil and gas exploration and
development continues to increase each
year on both private and BLM lands on
and around the Roan Plateau, where all
of the known Penstemon debilis
populations are found. In Garfield
County, 566 new wells were permitted
in 2003; 796 in 2004; 1,508 in 2005
(Colorado Oil and Gas Conservation
Commission (COGCC) 2006, p. 1); 1,844
in 2006; 2,550 in 2007 (COGCC 2008, p.
1); and 2,888 in 2008 (COGCC 2009, p.
1). Because of a decrease in natural gas
prices, new well permits decreased in
2009 to 743 (Webb 2009, p. 1; COGCC
2009, p. 1), but increased again to 1,887
in 2010, the highest for a county in
Colorado after Weld County (COGCC
2010, p. 17).
Energy exploration and development
activities include construction of new
unpaved roads, well pads, disposal pits,
evaporation ponds, and pipeline
corridors, as well as off-road travel by
employees. Each of these actions has the
potential to cause direct impacts to
Penstemon debilis, such as plant
removal and trampling, and indirect
impacts, such as dust deposition and
loss of habitat for pollinators. Because P.
debilis was unknown as a species until
1987, and the occurrences are on private
land or in remote locations on public
land, the impacts may go unnoticed. For
example, impacts to the Mt. Logan Mine
occurrence were unknown until the
occurrence was recorded in 2005. Even
after the discovery, further mine-related
impacts occurred because most of the
plants were on oil shale company land,
making it difficult for BLM to manage
the occurrence (CNHP 2010a, pp. 17–18;
Ewing 2009a, p. 4).
Road traffic on unpaved roads
increases dust emissions on previously
stable surfaces (Reynolds et al. 2001, p.
7126). For every vehicle traveling 1 mi
(1.6 km) of unpaved roadway once a
day, every day for a year, approximately
2.5 tons of dust are deposited along a
1,000-ft (305–m) corridor centered on
the road (Sanders 2008, p. 20). Vascular
plants can be greatly affected within the
zone of maximum dust fall (i.e., the first
410 ft (125 m) from the road) (Walker
and Everett 1987, p. 481). Excessive
dust may affect photosynthesis, affect
gas and water exchange, clog plant
pores, and increase leaf temperature,
leading to decreased plant vigor and
growth (Ferguson et al. 1999, p. 2;
Sharifi et al. 1997, p. 842). Because the
viable occurrences of P. debilis are
within 300 ft (91 m) of roads, well
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within the zone of maximum dust fall,
they are all likely to be affected by
decreased ability to photosynthesize,
impaired gas and water exchange,
clogged pores, and decreased plant vigor
and growth. However, traffic volume
and speed and dust generation within
300 ft (91 m) of the plants is currently
likely to be low, slow, and sporadic,
because reclamation and pad/road
construction within the occurrences is
mostly, but not entirely, completed.
Dust levels could increase at any time
depending on the amount of energy
development in the vicinity. We believe
that dust deposition has an impact on
the plants, but available information
does not indicate that the impact rises
to the level of a threat.
Other indirect impacts to Penstemon
debilis can occur due to loss of
pollinator habitat. P. debilis requires an
insect pollinator to reproduce
(McMullen 1998, p. iii). Prior to the
energy boom, McMullen (1998)
concluded that pollinators for P. debilis
were generalists and were not limiting
at that time. However, Tepedino (2009)
described the ways in which the
pollination biology of another Piceance
Basin rare plant, Physaria obcordata
(Dudley Bluffs twinpod), is impacted by
energy development. He described that
any energy development that reduces
the general level of available floral
vegetation has a detrimental effect on
pollinators’ ability to reproduce,
because fewer flowers provide less
nectar to feed the pollinators,
subsequently resulting in fewer
pollinators and reduced ability of the
dependent plant, such as P. debilis, to
produce seeds (Tepedino 2009, pp. 16–
17). The degree of impact on P. debilis
from loss of pollinator habitat due to
energy development is unknown, but is
not likely to rise to the level of a threat,
because disturbance of vegetated areas
adjacent to P. debilis occurrences is not
nearly as extensive as the foraging
distance of the pollinators.
A large parcel of land including
habitat occupied by both Anvil Points
occurrences was leased by the BLM for
oil and gas development in August 2008
(DeYoung 2008b, pers. comm.; DeYoung
2008c, pers. comm.; BLM 2008a, p. 1).
This proposed development is described
in the Roan Plateau Resource
Management Plan (RMP) Amendment,
which is still being contested in court
by environmental groups (Williams
2010). Increased energy exploration in
the Anvil Points Mine area may increase
maintenance and vehicle access on the
unstable road that transects the
Penstemon debilis occurrence and may
increase the likelihood of impacts to P.
debilis due to construction of additional
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roads and other facilities associated
with oil and gas exploration. Despite
ongoing disturbances, Anvil Points
Mine is the largest occurrence on
Federally managed land. If impacts
continue to modify or curtail this
habitat, the species is likely to become
in danger of extinction.
Oil Shale Extraction and Mine
Reclamation
Oil shale mining has likely impacted
Penstemon debilis occurrences. Access
roads for the mines at Anvil Points and
Mt. Logan were cut across cliff sides
occupied by the plants, displacing the
loose shale habitat and destroying
plants. Oil shale extraction activities
occurred on the Roan Plateau in the
early 1980s and into the 1990s (COBiz
2008, pp. 3–4). Because P. debilis was
not identified as a species until 1987,
we have no record of the pre-mining
occurrence status. However, we believe
the plants were present at these sites
prior to mining because some are still
present now. The plants were likely
heavily impacted by mine operations
within their habitat, and we think that
the occurrences are likely to have
recovered to a far smaller population
size on a reduced area of habitat (see
Factor E for discussion of inherent risk
of small population size).
Commercial oil shale extraction has
not yet proven to be economically
viable, and current research and
development efforts no longer focus
exclusively on surface mining of oil
shale rock on the Roan Cliffs (COBiz
2008, pp. 3–4). In November 2008, the
BLM issued its record of decision
approving resource management plan
(RMP) amendments to allow oil shale
leasing in the Piceance Basin (BLM
2007a, p. 1). The known Penstemon
debilis occurrences are not within the
area that BLM has currently identified
as available for oil shale leasing (BLM
2007a, p. 14). It is unknown when oil
shale extraction will become
economically viable. If commercial oil
shale production does become
economically viable, we expect a
renewed interest in extracting shale
from the cliffs of the Roan Plateau
because the shale is located
conveniently near the surface. Recent
impacts to the Anvil Points Mine plants
occurred due to energy production
research and removal of core samples by
an oil shale research and development
company (discussed below), and at the
Anvil Points Mine and Mt. Logan Mine
occurrences due to mine reclamation
and closure efforts (DeYoung 2009a,
pers. comm.; Mayo 2006, pp. 1–4).
The BLM conducted mine
reclamation actions under the
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Comprehensive Environmental
Response, Compensation, and Liability
Act (CERCLA) (42 U.S.C. 9601 et seq.),
commonly known as Superfund, to
remove health and safety hazards from
Anvil Points Mine. Actions included
closing access to the passages leading
into the mine and removing lead mine
tailings soil on the mine bench
(Goodenow 2008, pers. comm.). It is
unknown whether the lead in the soil is
a threat to Penstemon debilis. An
estimated 350 plants were on the mine
bench where the reclamation was done
(CNHP 2010a, p. 19). Eighty-eight plants
are known to have been directly
impacted by Anvil Points Mine
reclamation actions permitted by BLM
during 2008–2009 (DeYoung 2009b,
pers. comm.; Bennett 2010, pp. 1–2). Of
the 88, 21 plants that would have been
crushed by heavy equipment were
transplanted, 56 were covered by
matting intended to reduce soil
disturbance (DeYoung 2009b, pers.
comm.; DeYoung 2009c, pers. comm.),
and 11 plants were either covered with
tires or screened from human activities
with construction fencing (Bennett
2010, p. 2). As of December 2009, 17 of
the 88 plants were either dead or
unaccounted for (Bennett 2010, p. 2).
Any loss of plants at Anvil Points Mine
is a threat to the species because of the
small size of the entire population, but
we expect less disturbance at the site
now that reclamation is completed.
The BLM also allowed an oil shale
research and development company to
conduct research in the Anvil Points
Mine, a project area containing the
Anvil Points Mine occurrence (Ewing
2008a, pp. 4–6). This research consisted
of taking high resolution photographs of
the geologic formation visible from the
sides of the mine, and removal of stored
core samples. The project included
vehicle trips up the road every day for
1 month and directly impacted P.
debilis individuals growing in the road
immediately outside the mine (Ewing
2008a, pp. 4–6). The roads transecting
the occurrence are on shifting shale
talus slopes and are frequently subject
to rockslides and mudslides, which
require the road to be maintained
frequently. Three plants out of about
350 are known to have been destroyed
by the road maintenance conducted
under this permit (DeYoung 2009a, pers.
comm.). The BLM believes that some
additional plants may have been
trampled by unauthorized access to an
area that was fenced off during the
research period; however, it is unclear
how many plants were disturbed
(DeYoung 2008c, pers. comm.). In
addition to the direct impacts, the road
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maintenance required to allow this level
of traffic made occupied P. debilis
habitat more accessible to the public,
which could result in further trampling
by humans and vehicles (Ewing 2008a,
pp. 4–7).
The Mt. Logan Mine occurrence of
Penstemon debilis is primarily located
on land owned by Oxy oil shale
division, with a portion of the
occurrence occupying BLM land. This
occurrence is perched on a steep,
unstable slope above a road that is used
for access to an oil shale mine
reclamation project and for ongoing
maintenance of the site. Plants were
presumably removed to construct and
maintain the road during past mining
operations. Several plants out of 513
total on this steep road bank were
dangling by their roots in 2005 due to
road widening during reclamation
(Mayo 2006, pp. 1–4). The road was
widened farther, and these plants were
gone by 2006 (Mayo 2006, p. 1). Mine
reclamation actions destroyed about 30
of the 513 plants at another portion of
this occurrence by burying them in
topsoil (Ewing 2009a, p. 4). This site
also contains noxious weeds associated
with the disturbance, but it is unknown
whether the weeds will pose a threat to
P. debilis (Ewing 2009a, p. 4). The BLM
portion of this occurrence was included
in an oil and gas lease parcel nominated
for sale; however, BLM deferred the sale
of the lease parcel until completion of
their RMP revision (now scheduled for
May 2013) and until the Service
publishes a determination concerning
the status of the species (CNE 2005, p.
1; Lincoln 2009, pers. comm.). We
believe that the 513 plants counted at
this occurrence are a remnant of a larger
population that existed prior to mining
and reclamation activities. The potential
for further loss of plants at this location
is an ongoing threat that could
contribute to the species becoming in
danger of extinction within the
foreseeable future.
Road Construction and Maintenance
and Vehicle Access
The Anvil Points Mine occurrence
also is impacted during road
stabilization work by Garfield County,
which is done to maintain ongoing
access to a communications transmitter
tower located within occupied habitat
for Penstemon debilis on the mine
bench. We expect that continued
vehicle access through the plant habitat
will destroy a few plants at a time when
vehicles turn around and workers walk
on the shale slopes. Maintenance and
use of the road prevents reclamation of
the road bed, which would allow loose
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shale to cover the road and reclaim the
plant habitat along the mine bench.
The Mt. Logan Road occurrence,
located on the ROW above a heavily
traveled road near the Logan Mine
occurrence, had 10 plants in 1996, of
which only 3 plants were found in 2005
and again in 2010 (CNHP 2010, p. 22).
This occurrence has no barriers to
shield the plants from heavy dust
generated by truck traffic (CNHP 2010a,
p. 22; DeYoung 2009e, pers. comm.;
Ewing 2009a, p. 3). As a result of these
ongoing threats and the low number of
plants at the site, we consider this
occurrence to be nonviable.
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Summary of Factor A
In summary, three of the four viable
occurrences (Mt. Callahan and Mt.
Callahan Saddle Natural Areas and Mt.
Logan Mine) are on lands owned wholly
or partially by energy development
companies. Some individuals at the
fourth occurrence (Anvil Points Mine),
on BLM land, have been subject to
transplanting or destruction as a result
of a mine closure project and road
maintenance. Over the past 6 years, oil
and gas exploration and production has
increased substantially in the area
containing the habitat for Penstemon
debilis, making it likely that the species
will become in danger of extinction in
the foreseeable future. The pace of new
development slowed in 2009 because of
a variety of factors, but increased again
in 2010 (COGCC 2010, p. 17). P. debilis
grows on steep shifting slopes, and
roads through P. debilis habitat are
unstable and require frequent
maintenance, which destroys plants.
Plants seem to be able to recolonize
their habitat after disturbance; however,
recolonization is slow, and would not
be able to keep pace with rapid
development. For these reasons we
consider destruction and modification
of the species’ habitat for natural gas
production, oil shale mining, mine
reclamation, road maintenance,
exploration activities, and associated
impacts resulting from increased vehicle
access to the occurrences to constitute
an ongoing threat to P. debilis that may
cause the species to become in danger
of extinction within the foreseeable
future.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Activities resulting in overutilization
of Penstemon debilis plants for
commercial, recreational, scientific, or
educational purposes are not known to
exist. Therefore, we do not consider
overutilization for commercial,
recreational, scientific, or educational
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purposes to be a threat to the species
now or in the foreseeable future.
C. Disease or Predation
Seed predation of Penstemon debilis
by small mammals is very low
(McMullen 1998, pp. 39–40). Grazing,
predation, and disease are not known to
affect P. debilis. Therefore, we do not
consider disease or predation to be a
threat to the species now or in the
foreseeable future.
D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
Approximately 66.6 percent of
Penstemon debilis occupied habitat
occurs on private lands. We are not
aware of any city or county ordinances
or zoning that provide for protection or
conservation of P. debilis or its habitat.
Garfield County continues to maintain
and enlarge a communications
transmitter site within the Anvil Points
Mine occurrence without a permit from
BLM. Existing County ordinances fail to
address appropriate placement of
communications transmitters to avoid
impacts to sensitive species. The impact
may rise to the level of a threat if the
transmitter site is allowed to remain and
expand.
State Laws and Regulations
No State laws or regulations protect
rare plant species in Colorado.
Federal Policy and Management
The BLM manages the habitat for
about 19.4 percent of the Penstemon
debilis plants, on 33.3 percent of the
occupied habitat. Candidate species are
managed by BLM as sensitive species.
BLM has a policy for management of
sensitive species that recommends
avoidance and minimization of threats
to plants and habitat, as well as habitat
conservation assessments and
conservation agreements (BLM 2008c,
pp. 8, 36–38). No habitat conservation
assessments or conservation agreements
have been formalized for P. debilis.
The Federal Land Policy and
Management Act (FLPMA) (43 U.S.C.
1701 et seq.) directs BLM, as part of the
land use planning process, to ‘‘give
priority to the designation and
protection of areas of critical
environmental concern’’ (43 U.S.C.
1712(c)(3)). The FLPMA defines areas of
critical environmental concern (ACECs)
as ‘‘areas within the public lands where
special management attention is
required * * * to protect and prevent
irreparable damage to important
historic, cultural, or scenic values, fish
and wildlife resources or other natural
systems or processes, or to protect life
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and safety from natural hazards’’ (43
U.S.C. 1702 (a)). Designation as an
ACEC recognizes an area as possessing
relevant and important values that
would be at risk without special
management attention (BLM 2006, pp.
3–110). The ACEC designation carries
no protective stipulations in and of
itself (BLM 2006, pp. 2–65).
Following an evaluation of the
relevance and importance of the values
found in potential ACECs, a
determination is made as to whether
special management is required to
protect those values and, if so, to specify
what management prescriptions would
provide that special management (BLM
2006, pp. 3–111). The records of
decision (RODs) for the Roan Plateau
RMP Amendment were signed June 8,
2007, and March 12, 2008. The March
12, 2008, ROD designated the Anvil
Points ACEC, as an area for management
of sensitive resources including
Penstemon debilis (BLM 2008b, ROD p.
4). The ROD lists as an objective for the
Anvil Points ACEC to ‘‘protect occupied
habitat and the immediately adjacent
ecosystem processes that support
candidate plants.’’ This ROD also
authorizes oil and gas development in
the ACECs, making the portions of these
areas that are not currently leased
available for lease (BLM 2008b, ROD p.
2). Anvil Points ACEC covers most of
the formerly occupied occurrence area
at Anvil Points Rim, and the entire
Anvil Points Mine occurrence. At
present, no oil and gas development
activities are allowed. Implementation
of the RMP amendment, including lease
development, is dependent on the
outcome of litigation.
In order to protect Penstemon debilis
in the ACEC, a no surface occupancy
(NSO) and no ground disturbance (NGD)
stipulation was established for both
Anvil Points P. debilis occurrences
(BLM 2007b, ROD p. 26). The term NGD
applies to all activities except oil and
gas leasing and permitting, while the
term NSO applies only to oil and gas
leasing and permitting (BLM 2008b,
ROD p. 6). The NSO designation
prohibits long-term use or occupancy of
the land surface for fluid mineral
exploration or development to protect
identified resource values (BLM 2006,
pp. 2–3). This designation means that an
area is protected from permanent
structures or long-term grounddisturbing activities (i.e., lasting longer
than 2 years) (BLM 2006, pp. 2–3). For
example, an NSO designation would
preclude construction of a well pad
(because it would last longer than 2
years) but not a typical pipeline
(because it would be revegetated within
2 years) (BLM 2006, pp. 2–3). Also, an
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NSO does not preclude the extraction of
underlying fluid minerals if they can be
accessed from outside the area by
directional drilling (BLM 2006, pp. 2–3).
Directional drilling may not disturb the
overlying surface, including Penstemon
debilis habitat. Except for specified
situations, individual NSOs may
include exceptions so that BLM may
allow a ground-disturbing activity if it
meets specific, stated criteria (BLM
2006, pp. 2–3). For example, the NSO
designation for these occurrences allows
the BLM to grant exceptions for shortterm ground disturbing activities if a
conference with the Service indicates
that proposed activity would not impair
maintenance or recovery of the species
(BLM 2007c, pp. F6–F7).
The protections provided by the NSO/
NGD provision of the ACEC designation
are not adequate to provide for
maintenance of the Anvil Points Mine
occurrence because although BLM may
and usually does discuss plans with the
Service, they are not required to consult
with the Service and ensure that
proposed activity would not impair
maintenance or recovery of the species
prior to authorizing an exception to the
NSO/NGD (BLM 2007a, pp. F6–F7).
Consultation for a candidate or sensitive
species is not mandatory. Despite NSO/
NGD provisions, projects have
proceeded that resulted in destruction
of Penstemon debilis individuals. Other
actions with likely impacts to P. debilis
are still being considered by BLM
(DeYoung 2010, pers. comm.). This
ability to proceed with actions that
cause negative impacts to the species
indicates that the NSO/NGD provisions
do not fully protect P. debilis and its
habitat.
Recent examples demonstrating the
use of the NSO/NGD provisions were
discussed under Factor A. All of these
examples refer to the Anvil Points Mine
occurrence of Penstemon debilis:
(1) The BLM approved work under
the CERCLA to remove health and safety
hazards from the Anvil Points Mine
occurrence. While the BLM conferred
with the Service and minimized damage
to the plants ‘‘as much as was
practicable,’’ hazards to humans take
precedence over protecting candidate
plant species. This project resulted in
direct impacts to at least 88 Penstemon
debilis individuals (DeYoung 2009c,
pers. comm.).
(2) Also at the Anvil Points Mine, the
BLM is still considering granting
permission for continued maintenance
of the Garfield County transmitter tower
access road (DeYoung 2009b, 2010 pers.
comm.). Maintaining the existing tower
access road rather than relocating it
increases the likelihood of destroying P.
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debilis plants and prevents the
recolonization of plants in the current
road bed.
(3) The BLM has authorized oil shale
research projects in the past at the Anvil
Points Mine (Ewing 2008a, p. 4), which
led to the destruction of P. debilis plants
(BLM 2007c, pp. F6–F7; DeYoung
2009a, pers. comm.).
(4) The land containing the Anvil
Points Mine occurrence was leased for
oil and gas development under the BLM
August 2008 lease sale that is still
awaiting a court decision (DeYoung
2008b, p. 1; BLM 2008b, p. 1; Ewing
2008a, p. 7). Despite plant protections
built into the RMP amendment that is
now being challenged, increased energy
exploration in the Anvil Points Mine
area may increase maintenance and
vehicle access and consequently
increase the likelihood of destroying
plants
Summary of Factor D
We found that existing regulatory
mechanisms and agency policies do not
address the primary threats to
Penstemon debilis and its habitat. The
species was afforded some protection on
Federal lands as a candidate species;
however, candidate status has not
prevented impacts and threats to the
species from oil and gas development
and mine reclamation. Federal natural
resource laws do not protect Penstemon
debilis because they are not regulatory
unless the plant is proposed or listed,
and projects have occurred that have
continued to directly impact the
species. Furthermore, because much of
the plant population occurs on nonFederal lands, P. debilis has no
regulatory protection for approximately
81 percent of the total estimated plants.
Therefore, we determined that the
existing regulatory mechanisms do not
adequately address the primary threats
to the species.
E. Other Natural or Manmade Factors
Affecting the Species’ Continued
Existence
Failure of Transplants
The Anvil Points Rim occurrence,
which formerly included several
hundred plants on BLM land, was
reduced to zero plants in 1999 for
unknown reasons (CNHP 2010a, pp. 11–
12). It appears that the decline of this
occurrence was a result of natural
processes, including competition by
surrounding native vegetation, which
includes Chrysothamnus viscidiflorus
(yellow rabbitbrush) (DeYoung 2008a,
pers. comm.; CNHP 2010a, p. 12). Fiftythree Penstemon debilis seedlings
grown off site from seeds were
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introduced to Anvil Points Rim in 1996.
Ten survived until 2001, but all were
gone by 2005. Two mature plants found
in 2010 appear to be overlooked
survivors from the original population
(CNHP 2010a, p. 11). Monitoring failed
to show a cause for the decline of this
occurrence (DeYoung 2008a, pers.
comm.).
Small Population Size
Penstemon debilis population sizes
are small, and the smaller the
population, the more likely extinction is
in any given period of time (Shaffer
1987, p. 70). All occurrences of P.
debilis grow on a 17-mi (27-km) stretch
of the rim of the Roan Plateau in
Garfield County, Colorado (Ewing
2008a, p. 7). The two largest
occurrences are within 2 mi (3 km) of
each other (Ewing 2008a, p. 7). A
species with such a small range is
particularly susceptible to extirpation
from a stochastic event such as a
rockslide or severe hail storm
(McMullen 1998, p. 3). This increased
susceptibility is due to the likelihood
that, although stochastic events are
often localized in severity, such a
localized event would likely impact all
occurrences of the species, rather than
just a small portion of the occurrences,
as may be expected for a species with
a larger range. For example, the newly
discovered Smith Gulch location is
small (estimated 50 plants) and, because
of its positioning in a drainage, has a
high potential for being destroyed by a
rain event (DeYoung 2009d, pers.
comm.).
Habitat Fragmentation—Genetic
Diversity
In addition, the fragmentation of P.
debilis habitat by human-related
activities threatens to reduce the species
to mosaics of small populations
occurring in isolated habitat remnants.
Foraging pollinators spend more time
within large populations than small
populations, so sensitive plant species
with small populations (fewer than 50
individuals) are more likely to have a
lower seed set per individual than larger
ones, and to suffer genetic problems
such as genetic drift and inbreeding
depression due to losses of individuals
in such events such as those described
under Factor A (McMullen 1998, p. 3;
Ellstrand & Elam 1993, pp. 226, 228).
Genetic diversity of P. debilis is low
compared to other species of plants with
similar life-history traits (Wolfe 2010, p.
1), and thus the species is more
susceptible to genetic problems.
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Climate Change and Drought
Climate change could potentially
impact Penstemon debilis. The limited
geographic range of the oil shale
substrate that makes up the entire
Penstemon debilis habitat could limit
the ability of the species to adapt to
changes in climatic conditions by
progressive establishment of new
populations.
Incidental disturbance by humans and
stochastic events such as drought,
landslides, or encroaching vegetation
can impact Penstemon debilis. Climate
change could exacerbate these factors,
causing them to pose a threat to P.
debilis; however the current data are not
reliable enough at the local level for us
to draw conclusions regarding the
imminence of climate change threats to
P. debilis. The collective effects of small
population size, fragmented habitat,
genetic isolation, inability to shift with
climate changes, and failure of
reintroduction efforts make the species
vulnerable to destruction and
modification of its habitat, to the extent
that it is likely to become endangered
within the foreseeable future.
Cumulative Impacts
Some of the threats discussed in this
finding could work in concert with one
another to cumulatively create
situations that potentially impact
Penstemon debilis beyond the scope of
the combined threats we have already
analyzed. Destruction and modification
of habitat, and fugitive dust from truck
traffic, could reduce the number of other
species of blooming plants that attract
pollinators and could destroy the
ground-nesting habitat needed by bees.
A reduction in pollinators could cause
P. debilis to produce fewer seeds. Such
cumulative impacts may lower seed
production and reduce the number of
plants. We do not have documentation
that these cumulative impacts are
currently threatening the species.
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Summary of Factors
The primary factors threatening
Penstemon debilis are the present and
threatened destruction, modification, or
curtailment of its habitat and range, and
the inadequacy of existing regulatory
mechanisms to address the primary
threats to the species, exacerbated by
the collective impacts described under
Factor E. These factors pose imminent
threats to the species because they are
ongoing. The threats are moderated
because 39.8 percent of the occupied
habitat is protected by voluntary
conservation agreements, and 33.3
percent is managed to minimize some of
the threats, although 26.9 percent has no
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special management or protection. We
believe that the two main occurrences of
the species will be protected within the
State Natural Areas because Oxy is
implementing best management
practices during development. While
these actions may not prevent the
species from becoming endangered
when energy demands rise again, the
species is not likely to become in danger
of extinction within the foreseeable
future.
Species Information—Phacelia
submutica
Phacelia submutica is a rare annual
plant endemic to clay soils derived from
the Atwell Gulch and Shire members of
the Wasatch Formation in Mesa and
Garfield Counties, Colorado. The 9
populations and 22 known occurrences
of the plant occupy a total of 625.9 ac
(253.3 ha) (CNHP 2010a, pp. 24–82;
Service 2011a, p. 7). All occurrences
consist of small patches of plants on
uniquely textured, shrink-swell clay soil
separated by larger areas of similar soils
that are not occupied by P. submutica.
The estimated total number of plants
ranges from 7,767 to 68,371 per year,
depending on growing conditions. In
some years, surveyors have failed to
find any plants. The species depends on
its seed bank to survive for one or many
years, again depending on growing
conditions.
Taxonomy
Phacelia submutica was first
described by Howell based on
specimens collected from the town of
DeBeque, Mesa County, Colorado, in
1911 and 1912 (Howell 1944, pp. 370–
371). Halse (1981, pp. 121, 129, 130)
reduced it to varietal status as P.
scopulina var. submutica. Halse’s
nomenclature has been challenged by
O’Kane (1987, p. 2), who claimed Halse
used inadequate collection materials
and that P. submutica is geographically
isolated from P. scopulina (O’Kane
1987, p. 2; 1988, p. 462). Phacelia
submutica is the recognized species
name in current floristic treatments in
Weber and Wittmann (1992, p. 98; 2001,
p. 203) and by the Director of the Biota
of North America Program (Kartesz
2008, pers. comm.). While the Integrated
Taxonomic Information System (2001)
database cites John Kartesz as the expert
source for this species, it is not updated
with his currently accepted name for the
species: Phacelia submutica (Kartesz
2008, pers. comm.). Because the weight
of evidence indicates that Phacelia
submutica is the appropriate species
name, we are listing the species with
this nomenclature. Phacelia is included
in the Hydrophyllaceae (waterleaf)
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family. Recent molecular data suggest
that this family should be combined in
an expanded Boraginaceae (borage)
family. Conflicting views exist on the
configuration of this larger
Boraginaceae. The lead author of the
family treatment for the upcoming Flora
of North America has chosen to retain
the Hydrophyllaceae. Therefore, we will
retain Phacelia in the Hydrophyllaceae
family for this final rule.
Description
Phacelia submutica is a low-growing,
herbaceous, spring annual plant with a
tap root. The stems are typically 0.8 to
3 in (2 to 8 cm) long, often branched at
the base and mostly lying flat on the
ground as a low rosette (Howell 1944,
pp. 371–372). Stems are often deep red
and more or less hairy with straight and
stiff hairs. Leaves are similarly hairy,
reddish at maturity, 0.2 to 0.6 in (5 to
15 mm) long, egg-shaped or almost
rectangular with rounded corners, with
bases abruptly tapering to a wedgeshaped point. Leaf margins are smooth
or toothed. The tube-shaped flowers are
yellowish white, on short stems; the 5
petals are 0.16 to 0.19 in (4–5 mm) long;
the stamens do not protrude beyond the
petals. The style is 0.04 to 0.06 in (1 to
1.5 mm) long and nearly hairless, and
the seed capsules do not have a short,
sharply pointed tip (Howell 1944, pp.
371–372; Halse 1981, p. 124). The
elongated egg-shaped seeds are 0.6 to
0.8 in (1.5 to 2 mm) long with 6 to 12
crosswise corrugations, and are blackish
brown and somewhat iridescent (Howell
1944, p. 370; Halse 1981, p. 130; O’Kane
1987, p. 3).
Seed Bank
Phacelia submutica plants flower
between late April and late June and set
seed from mid-May through late June.
Individuals finish their life cycle by late
June to early July, after which time they
dry up and disintegrate or blow away,
leaving no indication that the plants
were present (Burt and Spackman 1995,
p. 23). The species grows in a habitat
with wide temperature fluctuations,
long drought periods, and erosive saline
soils. Upon drying, cracks form in the
shrink-swell clay soils. Seeds plant
themselves by falling into the cracks
that close when wetted, thus covering
the seeds (O’Kane 1988, p. 20).
Phacelia submutica seeds can remain
dormant for 5 years (and probably
longer) until the combination and
timing of temperature and precipitation
are optimal for germination (CNHP
2010a, pp. 24–82). The ideal conditions
required for seed germination are
unknown, but it is likely that
germination depends not on total
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precipitation but on the temperature
after the first major storm event of the
season (Levine et al. 2008, p. 795). Rare
annuals that flower every year are
subject to extinction under fluctuating
conditions, because they exhaust their
seed reserves (Meyer et al. 2006, p. 901).
Rare ephemeral annuals, such as P.
submutica, that save their seed bank for
the best growing conditions are more
resilient to fluctuating conditions. P.
submutica numbers at Horsethief
Mountain fluctuated from 1,700 plants
in 1986, to 50 in 1992, up to 1,070 in
2003, and down to only a few from 2006
to 2008 (CNHP 2010a, pp. 49–50). The
fluctuation in numbers indicates that
many seeds remain dormant in the seed
bank during years when few plants can
be found. We do not know how long the
seeds can remain viable in the soil.
Although plant sites differ in numbers
of flowering plants each year, there are
no observations of site expansion.
Habitat
Phacelia submutica is restricted to
exposures of chocolate to purplish
brown and dark charcoal gray alkaline
clay soils derived from the Atwell Gulch
and Shire members of the Wasatch
Formation (Donnell 1969, pp. M13–
M14; O’Kane 1987, p. 10). These
expansive clay soils are found on
moderately steep slopes, benches, and
ridge tops adjacent to valley floors of the
southern Piceance Basin in Mesa and
Garfield Counties, Colorado. On these
slopes and soils, P. submutica usually
grows only on one unique small spot of
ground that shows a slightly different
texture, color, and crack pattern than
the similar surrounding soils (Burt and
Spackman 1995, p. 15). We do not have
a precise scientific description of the
soil features required to support this
species. The natural shrink-swell
cracking process creates the conditions
needed for the plants and seed bank to
thrive.
Distribution
The currently known occupied habitat
where the plants grow occurs on about
625.9 ac (253.3 ha) (CNHP 2010a, pp.
24–82). About 80.9 percent of the
occupied habitat is on lands managed
by the BLM, 11.9 percent is on private
lands, 6.4 percent is on lands managed
by the USFS, and 0.7 percent is on lands
managed by the Colorado Division of
Wildlife (CDOW) (Service 2011a, pp. 6–
7). A general range encompassing
outlying occurrences of Phacelia
submutica includes about 82,231 ac
(34,896 ha) (Service 2011a, p. 13). The
growing town of DeBeque and about 10
mi (16.4 km) of Interstate 70 and the
Colorado River bisect the species’ range.
Phacelia submutica is classified by
the CNHP as a G2 and S2 species, which
means it is imperiled across its entire
range and within the State of Colorado
(CNHP 2010b, p. 12). The CNHP ranks
the quality of each occurrence on a scale
of A to E, with A meaning an excellent
occurrence that is abundant and viable;
B, C, and D meaning good, fair, and
poor, respectively; and E meaning the
occurrence still exists, but no ranking
information is available. Historical
records (H rank in Table 3, below) have
not been revisited for 20 years or more.
Ranks are based on the viability and
number of plants, the amount of
anthropogenic (human) disturbance,
and the amount of weed cover and
intact habitat (CNHP 2010b, pp. 12–13).
No occurrences of Phacelia submutica
have been found beyond the described
habitat and range. Surveys for P.
submutica have been conducted
outward from DeBeque as far as the
exposed soil members extend within the
geologic formation (Burt and Spackman
1995, p. 14). Surveys in 2010 added 148
ac (60 ha) of new locations within the
known range of the species.
TABLE 3—Phacelia submutica OCCURRENCES WITHIN POPULATIONS BY LANDOWNERSHIP (ACRES (AC) (HECTARES (HA))
(CNHP 2010a, pp. 24–82, observation dates 1982 to 2010; WestWater Engineering 2007, pp. 16, 17, 19, 27; Kirkpatrick 2011, pers. comm.;
Potter 2010, Wenger 2010; Lyon 2010, pers. comm.; Service 2011a; CNHP 2010b, pp. 12–13)
High counts
estimates
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Population occurrences
SULPHUR GULCH:
Sulphur Gulch ..............................
Winter Flats Sulphur Gulch .........
PYRAMID ROCK:
Pyramid Rock ..............................
Pyramid Ridge Coon Hollow
South.
Coon Hollow/B/C .........................
Mount Low West of DeBeque .....
Dry Fork Roan Creek ..................
Bloat Gulch Logan Wash .............
Coon Hollow ................................
ROAN CREEK:
Roan Creek ..................................
DEBEQUE
DeBeque West .............................
DeBeque East Cemetery Road ...
MOUNT LOGAN:
Mount Logan ................................
ASHMEAD DRAW:
South of DeBeque .......................
DeBeque Reservoir Ashmead
Draw.
BAUGH RESERVOIR:
Baugh Reservoir ..........................
HORSETHIEF MOUNTAIN:
Jerry Gulch ..................................
Moffat Gulch ................................
S of Horsethief Creek ..................
Housetop Mtn. Jerry Gulch Atwell
Gulch.
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Habitat
ac
Low counts
Habitat
ha
Viability
rank*
Owner
70
35
0
25
4.4
9.7
1.8
3.9
H
D
BLM.
BLM.
3,050
1,500
1
2
213.6
55.4
86.4
22.4
BC
B
BLM.
BLM.
11,000
10,000
800
5,820
200
42
300
100
0
150
58.4
15.9
24.2
50.2
2.1
23.6
6.4
9.8
20.3
0.8
AB
B
BC
H
H
BLM.
BLM, Private.
BLM, Private.
BLM, Private.
BLM.
195
21
5.8
2.3
C
Private.
500
20
0
0
14.8
36.2
6.0
14.6
H
D
BLM, Private.
BLM.
50
5
7.0
2.8
C
BLM.
17
210
0
0
3.9
16.8
1.6
6.8
H
C
BLM.
BLM, Private.
1,000
0
6.1
2.5
H
BLM, Private.
300
20
55
4,000
200
0
10
235
3.2
2.0
2.0
20.4
1.3
0.8
0.8
8.2
C
H
C
B
Private.
BLM.
BLM.
BLM, USFS.
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TABLE 3—Phacelia submutica OCCURRENCES WITHIN POPULATIONS BY LANDOWNERSHIP (ACRES (AC) (HECTARES
(HA))—Continued
(CNHP 2010a, pp. 24–82, observation dates 1982 to 2010; WestWater Engineering 2007, pp. 16, 17, 19, 27; Kirkpatrick 2011, pers. comm.;
Potter 2010, Wenger 2010; Lyon 2010, pers. comm.; Service 2011a; CNHP 2010b, pp. 12–13)
High counts
estimates
Population occurrences
Low counts
Habitat
ac
Habitat
ha
Viability
rank*
Owner
Horsethief Mtn. NW.–SW.–WSW.
Shire Gulch.
ANDERSON GULCH:
Anderson Gulch Round Mtn. .......
14,429
5,300
69.1
28
C
USFS, BLM, Private.
15,100
1,376
4.5
1.8
A
Private, State.
Totals ....................................
68,371
7,767
625.9
253.3
* An A indicates those occurrences with the highest number of individuals and best habitat, while a D represents those occurrences with the
fewest individuals and degraded habitat. An H represents an occurrence that has not been re-visited in over 20 years.
Summary of Factors Affecting Phacelia
submutica
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Phacelia submutica is threatened with
destruction and modification of its seed
bank and habitat due to the following
issues: modification of areas for oil and
natural gas exploration and production,
development of the Westwide Energy
Corridor, increased access to the habitat
by off-road vehicles (ORVs), soil and
seed disturbance by livestock and wild
ungulates, and proposed water reservoir
projects. All known occurrences are in
the midst of the second largest natural
gas-producing area in Colorado (COGCC
2010).
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Natural Gas Development
About 78 percent of the habitat for the
species and 67 percent of the entire
range of Phacelia submutica are on BLM
lands currently leased for oil and gas
drilling (Ewing 2009, map). An
additional 65 ac (26 ha) of habitat (10
percent) may be opened to natural gas
development by BLM pending
development of a new RMP for the
Grand Junction Field Office in 2013
(Ewing 2008a; BLM 2005, p. 5). About
3 percent of the habitat is on private
land owned by energy companies (Burt
and Spackman 1995, p. 25). Although
the sale of oil and gas leases by BLM
does not directly impact rare plant
habitat, it indicates the intention to
continue and increase the level of
development in an area that covers a
large portion of the range of P.
submutica. Likewise, the Colorado Oil
and Gas Conservation Commission
(COGCC) issues permits to drill that
indicate imminent development at
specific sites on private and Federal
lands (COGCC 2009b, pp. 1–3). COGCC
issued 10 new drilling permits in 2009.
Within the range of P. submutica, there
are 178 natural gas wells; 60 of these
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wells are located within the same 640 ac
(259 ha) section as 18 of the 22
occurrences of the species (Ewing
2009b, map).
Five occurrences of Phacelia
submutica are located on BLM land in
an area called South Shale Ridge that
covers more than a third of the known
range for this species (BLM 2005, p. 5).
Part of South Shale Ridge was
recommended as an ACEC for
protection of P. submutica in 1995, but
was not designated as an ACEC (Burt
and Spackman 1995, p. 36) in that area.
Portions of South Shale Ridge that were
withheld from leasing in the past were
leased for oil and gas development in
November 2005 (BLM 2005, p. 5). These
leases were subsequently deferred
pending development of a new RMP for
the Grand Junction Field Office (Ewing
2008c, pers. comm.; BLM 2005, p. 5).
The new RMP is now scheduled for May
2013, and the leases are still on hold
(Ewing 2011, pers. comm.). If the BLM
sells these leases, then 8 ac (3 ha) of
occupied P. submutica habitat within
about 65 ac (26 ha) of suitable habitat
will be newly opened to natural gas
development in a previously
undeveloped area (Ewing 2009, map),
with additional impacts anticipated
from associated roads and related
development.
Pyramid Rock is adjacent to South
Shale Ridge, and the Pyramid Rock
occurrence of Phacelia submutica is
within the BLM Pyramid Rock ACEC,
including an estimated 1 to 3,050 plants
(depending on the year) within 214 ac
(86 ha) of habitat (CNHP 2010a, p. 29;
Wenger 2009, pp. 1–11; Wenger 2010, p.
3). Stipulations of no new surface
occupancy or ground disturbance apply
to this ACEC for protection of candidate,
proposed, and listed plant species.
These stipulations do not apply to
sensitive species. However, due to the
possibility of exceptions being granted,
we cannot predict with any degree of
certainty what stipulations will actually
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be applied to the plant or its habitat that
ensure the long-term conservation of the
species. The BLM installed cable fence
in 2007 to deter ORVs from crossing
habitat for the Federally threatened
cactus Sclerocactus glaucus (Colorado
hookless cactus) and P. submutica. Only
a few ORVs have left tracks under the
fence and across P. submutica habitat.
The BLM excluded this ACEC from a
South Shale Ridge lease sale in 2005
(BLM 2005, p. 5). P. submutica plants
have not been directly impacted since
the fence was installed, and existing
pipeline and roads remain outside the
fence. The ACEC has provided some
protection thus far for about 4 percent
of the plants (see Table 3 above).
We recommend buffers of 656 ft (200
m) for pipeline ROWs between the edge
of disturbance and suitable plant habitat
to protect the plants from destruction by
vehicles that stray outside of the project
area, runoff, erosion, dust deposition, or
other indirect effects such as destruction
of pollinator nesting habitat. In spite of
such efforts, pipeline ROWs exist within
20 ft (6 m) and 100 ft (30 m) of known
P. submutica occurrences (Lincoln
2008, pers. comm.).
The ongoing threats to habitat that are
associated with oil and gas development
include well pad and road construction;
installation of pipelines; and
construction of associated buildings,
holding tanks, and other facilities. All of
these actions would destroy the seed
bank of Phacelia submutica and modify
its habitat so that the plants could no
longer grow in these areas.
Westwide Energy Corridor
The Energy Policy Act of 2005 (42
U.S.C. 15801 et seq.) directs the
Secretaries of Agriculture, Commerce,
Defense, Energy, and the Interior to
designate energy transport corridors for
oil, gas, and hydrogen pipelines and
electricity transmission and distribution
facilities on Federal lands in certain
western U.S. States. A portion of the
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designated Westwide Energy Corridor
crosses 16,326 ac (6,621 ha) of BLM
land within the range of Phacelia
submutica. Nine of the species’ 22
occurrences are located within this
energy corridor (Westwide 2009, map;
Ewing 2009, map). Pipeline and
transmission line routes along the
energy corridor are not yet identified,
but it is not feasible that all habitat for
P. submutica will be avoided as the
corridor continues to be developed.
Cumulative Impacts of Energy
Development
Energy development activities
described above are occurring in close
proximity to Phacelia submutica
locations (WestWater Engineering 2004,
p. 11). Oil and gas pipelines, well pads,
and access roads are present on 11 P.
submutica occurrences (CNHP 2010a,
pp. 24–82). Frequently travelled roads
bisect and cross the edges of nine
occurrences. It is likely that some of the
seed bank was displaced or destroyed to
build the roads and pipelines. On
Federal lands, direct impacts to known
plant locations are mostly being avoided
by careful placement of pipelines, well
pads, and associated facilities, due to
the candidate status of the species.
Our concern is primarily for the
cumulative impacts of energy
development. When all of the oil and
gas wells are connected to the system of
local pipelines, roads, and pumping
stations, in combination with crosscountry transmission lines and
pipelines, more ROWs will be
necessary. Under these conditions, it is
difficult to protect occupied or potential
habitat for P. submutica. The natural
shrink-swell cracking process creates
the soil conditions needed for P.
submutica and its seed bank to thrive;
however, the natural soil surface
structure is fragile and easily disturbed.
Blading of the top few inches of soil
during well pad and road construction,
installation of underground pipelines,
and construction of associated
buildings, holding tanks, and other
facilities alter the unique soil structure,
especially when it is wet, and may
disturb, damage, or remove seed banks
that are critical to the survival of this
species. Any ground disturbance that
churns or compacts the soil or changes
the shrink-swell crack structure is likely
to have a deleterious effect on the in situ
seed bank and, therefore, on successful
plant recruitment and survival of the
species in subsequent years (Meyer et al.
2005, p. 22).
Off-Road Vehicle Recreation
Energy development increases access
to previously roadless areas, which
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encourages ORV traffic to drive on
nearby slopes that support plant habitat.
ORV use occurs on BLM lands in the
general vicinity of Phacelia submutica
and has been recorded within occupied
habitat at seven occurrences (CNHP
2010a). The vehicles stray from
designated roads to climb hills for
recreational purposes (Mayo 2008d,
photo). Substantial surface disturbance
due to churning by ORV tires can alter
the unique soil structure required by
this species, with the same negative
effects on the seed bank as described
above.
Trampling
Trampling of the habitat by livestock
and wildlife is documented at 14 of the
22 occurrences (CNHP 2010a, pp. 24–
82). Substantial surface disturbance due
to heavy trampling increases soil
compaction and erosion and alters the
microhabitat, such as the cracked soil
surface, the species requires.
Livestock-related impacts have
resulted in the loss of similar plant
species in other locations. Lepidium
papilliferum (slickspot peppergrass) is a
rare ephemeral annual desert plant in
Idaho (comparable to Phacelia
submutica), which has highly specific
soil requirements and which depends
on its seed bank. The slickspot
peppergrass population dropped from
thousands of plants in 1995, to no new
plants after intensive trampling when
the soil was wet and seeds were
germinating (Meyer et al. 2005, p. 22).
The population has not recovered,
which is believed to be due to damage
and burying of seeds that prevented
them from germinating. After 11 years of
monitoring, researchers have clear
evidence that ‘‘any form of soil
disturbance is likely to have a
deleterious effect on the in situ seed
bank,’’ and that all potential habitat for
such a species (such as P. submutica)
should be managed as if it were
currently occupied (Meyer et al. 2005,
p. 22).
Water Reservoirs
Two water reservoir projects known
as Roan Creek and Sulphur Gulch have
been proposed in the past within
occupied habitat of Phacelia submutica.
The potential reservoir locations would
have impacted two occurrences.
Recently, both projects were again
evaluated as potential reservoirs to
provide a water supply for in-stream
flows for endangered fishes in the
Colorado River (Friedel 2004, p. 1;
Grand River Consulting Corporation
2009, p. 3). After evaluation of
numerous alternatives, the Sulphur
Gulch and Roan Creek projects are no
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45071
longer being considered as a water
supply for endangered fishes because
more practical sources were found (Bray
and Drager 2008, pers. comm.; Grand
River Consulting Corporation 2009, pp.
1–5). The Roan Creek reservoir project
also was proposed by Chevron Shale Oil
Company and Getty Oil Exploration
Company to be used for development of
oil shale extraction (Chevron-Getty
2002, pp. 2, 8), but the oil shale projects
were not developed. These potential
reservoirs could permanently destroy
plants and their habitat by project
construction and inundation. Because
the proposals have been withdrawn,
these threats are not imminent;
however, the sites have been identified
as potential reservoir locations that
could be developed within 20 years if
warranted by increased demands for
water. Increased demands are likely,
depending on the oil shale market,
urban development in Colorado, and
less precipitation due to climate change.
Summary of Factor A
We consider destruction,
modification, and fragmentation of
habitat to be moderate threats to
Phacelia submutica throughout its
range, due to ongoing development of
oil and gas with associated pipelines,
construction of new road and utility
ROWs, road widening, and construction
of access roads. P. submutica habitat
also is threatened by soil modification
resulting from livestock trampling and
ORV tracking. These threats are of
moderate magnitude because at least 14
of the 22 occurrences are being
impacted to some degree by one or more
of the threats, and because the plants
and their seed banks occur in small,
isolated patches that are easily
destroyed by small-scale disturbances. If
these threats increase in frequency,
severity, or scope, the species is likely
to become in danger of extinction
within the foreseeable future.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Activities resulting in overutilization
of Phacelia submutica plants for
commercial, recreational, scientific, or
educational purposes are not known to
exist. Therefore, we do not consider
overutilization for commercial,
recreational, scientific, or educational
purposes to be a threat to the species
now or in the foreseeable future.
C. Disease or Predation
Disease or herbivory are not known to
affect Phacelia submutica. Therefore,
we do not consider disease or predation
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to be a threat to the species now or in
the foreseeable future.
D. The Inadequacy of Existing
Regulatory Mechanisms
Local Laws and Regulations
County ordinances or zoning are not
known to affect Phacelia submutica or
its habitat. Therefore, we do not
consider inadequacy of existing local
laws and regulations to be a threat to the
species now or in the foreseeable future.
State Laws and Regulations
No State regulations protect rare plant
species in Colorado. The CNAP has
entered into agreements with BLM to
help protect the Pyramid Rock ACEC
occurrence of Phacelia submutica by
also managing it as a designated State
Natural Area that is monitored by
volunteer stewards. The Pyramid Rock
occurrence has been adequately
protected thus far, but the management
agreement can be terminated with 90day written notice by either party.
Therefore, we have concluded that the
State Natural Area designation alone
does not constitute a regulatory
mechanism to conserve P. submutica.
Federal Laws and Regulations
mstockstill on DSK4VPTVN1PROD with RULES2
Bureau of Land Management
Candidate species are managed by
BLM as sensitive species. Sensitive
species designations provide policies to
be carried out with the resources
available, but they do not provide
regulations to protect this species from
losing habitat and seed banks to energy
development projects. The BLM
attempts to avoid disturbances that
would adversely affect sensitive species’
viability or trend the species toward
Federal listing. This includes avoidance
of suitable habitat if it can be identified
as such (BLM 2008c, pp. 8, 36; BLM
2008d, pp. 5–7). However, the BLM
policy of avoidance and minimization of
threats to plants and habitat may not
adequately protect Phacelia submutica
because the plants can only be found for
a few weeks during years when growing
conditions have been favorable (Burt
and Spackman 1995, p. 8). Thus, wellintentioned avoidance and
minimization measures may not be
implemented if no plants are seen, even
in areas where subsequent timely
surveys would likely demonstrate a
persistent seed bank. As opposed to
listed species, biological assessments or
consultation with the Service are not
required for BLM-designated sensitive
species during the authorization process
for oil and gas use on Federal lands
(BLM 2008d, p. 33).
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Section 365 of the Energy Policy Act
of 2005 (42 U.S.C. 15801 et seq.)
establishes a Federal Permit
Streamlining Pilot Project with the
intent to improve the efficiency of
processing oil and gas use
authorizations on Federal lands. The
two BLM pilot project offices for
Colorado are in the Colorado River
Valley and Grand Junction Field Offices,
both of which manage Phacelia
submutica habitat. Faster processing of
permits to drill increases the likelihood
of ground disturbance on P. submutica
habitat because the plants are ephemeral
annuals that can only be found for about
6 weeks during favorable years, and not
all of the habitat has been surveyed.
When the plants are not present or
previously documented, avoidance of
the seed bank depends on field
assessments of habitat. As a result, seed
banks and habitat are increasingly likely
to be disturbed or removed during the
process of approving locations for new
energy development projects.
U.S. Forest Service
Phacelia submutica is currently on
the sensitive species list for the USFS,
Region 2 (USFS 2009). The USFS
manages 6.4 percent of the habitat for P.
submutica (Service 2011a, p. 9).
Trampling by mule deer and trespass
cattle has damaged plants and habitat at
two sites on the Grand Mesa National
Forest; ORVs have impacted another site
(USFS 2010; CNHP 2010a, pp. 24–82).
Most of the habitat is protected from
access by steep badlands and canyons.
The habitat is open to oil and gas
leasing with an NSO stipulation.
A Proposed Research Natural Area to
protect the species on the White River
National Forest has not been formally
established (Proctor 2010, pers. comm.).
If established, protection would include
restrictions on ORV use, livestock
grazing, and resource extraction.
Regulatory mechanisms on USFS lands
do not protect the species, because such
restrictions are not in place, and the
NSO stipulation can be waived in some
cases.
Summary of Factor D
We have determined that existing
regulatory mechanisms do not address
the primary threats to P. submutica
because the existing RMPs do not
provide protection from the threat of oil
and gas development. The one ACEC in
place is not adequate to protect the
species because it includes only 4
percent of the habitat. Sensitive species
designations provide policies to be
carried out with the resources available,
but they do not provide regulations to
protect this species from losing habitat
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and seed banks to energy development
projects, cattle trampling, or ORV traffic
over the next 10 to 20 years.
E. Other Natural or Manmade Factors
Affecting the Species’ Continued
Existence
Climate Change
Climate change is likely to affect
Phacelia submutica because seed
germination, seed dormancy, and
persistence of the seed bank are all
directly dependent on precipitation and
temperature patterns (Levine et al. 2008,
p. 805). As described under Factor E for
Ipomopsis polyantha, climate modeling
is not currently to the level that we can
predict the amount of temperature and
precipitation change within the limited
range of P. submutica.
Future changes in the timing of and
temperatures associated with the first
major spring rains each year may more
strongly affect germination and
persistence of ephemeral annual plants
than changes in the amount of seasonlong rainfall (barring severe droughts)
(Levine et al. 2008, p. 805). Likewise,
increasing environmental variance, such
as an unusually wet spring, might
decrease extinction risk for rare desert
ephemeral plants, because they
typically rely on extremely good years
to restock the persistent seed bank,
while extremely bad years have little
impact (Meyer et al. 2006, p. 901). A
persistent seed bank enables the species
to survive drought. However, extremely
long droughts resulting from climate
change, with no good years for
replenishing the seed bank, would
likely cause Phacelia submutica to
become endangered. Because the soil
can remain bare of P. submutica plants
for several years, it is difficult to
identify and protect the seemingly
unoccupied habitat that occurs in small,
isolated patches that are easily
destroyed by small-scale disturbances,
and can be overlooked during habitat
assessments. The longer the species
remains dormant, the less likely it is
that we will know if an area is occupied,
reducing our ability to avoid impacts to
the species and protect it from becoming
endangered.
We do not yet have information on
the species’ pollinator needs sufficient
to predict the effects of climate change
on pollinator-plant interactions for this
species.
Summary of Factor E
While current climate change
predictions are not reliable enough at
the local level for us to draw
conclusions about its effects on P.
submutica, it is likely that there will be
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drying trends in the future and the seeds
will remain dormant for long periods.
This would make it increasingly
difficult to detect occupied habitat and
avoid destruction of habitat, and more
likely that the species will become
endangered. Because its seed bank is
vital to the survival of Phacelia
submutica, the potential impacts of
climate change (described above) are
likely to make the species more
vulnerable to the threats described
under Factor A to an extent that the
species may become endangered within
the foreseeable future.
Summary of Factors
The current range of Phacelia
submutica is subject to human-caused
modifications from natural gas
exploration and production with
associated expansion of pipelines,
roads, and utilities; development within
the Westwide Energy Corridor;
increased access to the habitat by ORVs;
soil and seed disturbance by livestock
and wildlife (Factor A).
The main reason that the species is
vulnerable to energy development is
that the plants’ annual life cycle only
lasts a few weeks before they dry up and
blow away, and they may not appear at
all for several years if growing
conditions are not favorable. With such
a short life cycle and unpredictable
emergence, occupied habitat may not be
recognized as such, so it may be
inadvertently destroyed.
Protecting the seed bank in the soil
depends on avoiding ground
disturbance of bare patches of clay soil
where nothing appears to be growing
most of the time. The plants and their
seed banks occur in small, isolated
patches that are easily destroyed by
even small-scale disturbances. The
species’ small geographic range, highly
specific soil and germination
requirements, limited seed dispersal,
fragmented habitat, prolonged seed
dormancy, and potential seed bank
depletion by prolonged drought (Factor
E) make P. submutica vulnerable to the
threats in Factor A to an extent that the
species may become endangered within
the foreseeable future, depending
primarily on the rate of future energy
development. The plants do not
disperse seeds beyond the existing
patches of unique soil that are separated
from one another by a few yards or
several miles. Any loss of occupied
habitat will be a permanent loss for the
foreseeable future, and cause a decline
in the status of the species.
Determination
We have carefully assessed the best
scientific and commercial information
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available regarding the past, present,
and future threats to Ipomopsis
polyantha, Penstemon debilis, and
Phacelia submutica.
Ipomopsis polyantha
We find that the present and
threatened destruction, modification, or
curtailment of Ipomopsis polyantha
habitat is a threat to the species’
continued existence. Ongoing and
planned commercial, municipal, and
residential development; associated
road and utility improvements and
maintenance; and competition from
introduced roadside grasses (as
discussed under Factor A above) pose a
significant threat to the species. The
resulting modifications of the species’
habitat will likely relegate the plants to
small, fragmented portions of highway
ROWs and a few small, lightly used,
private pastures, within 5 to 10 years,
depending on the real estate market. At
that point the species would no longer
be resilient or viable, indicating that the
species is in danger of extinction across
its entire range.
Ipomopsis polyantha also is
threatened by concentrated livestock
trampling of plants and soil and some
herbivory (as discussed under Factor C).
Livestock grazing may decrease in the
future, but mowing and landscaping is
likely to increase with higher density
development within the next few years.
Predation is an ongoing threat of
moderate magnitude and severity,
which, combined with the threat of
habitat modification under Factor A,
could cause the species to become
extinct within the foreseeable future.
The existing regulatory mechanisms
do not address the threats to the species
or its habitat. The absence of regulatory
mechanisms exacerbates the threats
discussed under Factor A.
The natural and human-caused factors
of specific soil and germination
requirements, fragmented habitat,
effects of drought and climate change,
and lack of proven methods for
propagation and reintroduction (as
discussed under Factor E) present an
ongoing and moderate degree of threat
to Ipomopsis polyantha across the entire
range of the species. This factor alone is
not likely to cause the species to become
extinct, but it impacts the species’
ability to withstand and recover from
the threats discussed under Factors A
and C.
On the basis of the best available
information, we are listing Ipomopsis
polyantha as an endangered species.
Endangered status reflects the
vulnerability of this species to threat
factors negatively affecting it and its
limited and restricted habitat. This
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45073
species is beyond threatened status, or
beyond the point of being likely to
become an endangered species within
the foreseeable future. Ongoing threats
to the species and its habitat (discussed
under Factors A and C) are such that it
is currently in danger of extinction
throughout all of its range, meeting the
definition of an endangered species as
defined in the Act. We have determined
that I. polyantha is in danger of
extinction throughout all of its range.
Penstemon debilis
Penstemon debilis is threatened with
destruction and modification of its
habitat due to ongoing and foreseeable
threats that include oil and gas
development, oil shale extraction and
mine reclamation, road construction
and maintenance, and vehicle traffic
throughout its habitat (as discussed
under Factor A above). These threats are
of high magnitude across more than half
of the species’ limited range. We believe
that the effects of these threats are likely
to cause Penstemon debilis to become
an endangered species within the
foreseeable future.
The existing regulatory mechanisms
do not address the threats to the species
or its habitat. The absence of regulatory
mechanisms exacerbates the threats
discussed under Factor A. Local or State
regulations of plant species’ habitats are
nonexistent. Existing Federal regulatory
mechanisms are only partially effective
at ameliorating threats to plants and
habitat (as discussed under Factor A).
Stipulations for Federal protection of
habitat are planned but not yet
implemented (as discussed under Factor
A). Private landowner agreements with
the State currently protect 69 percent of
the habitat, but their continuation is not
guaranteed.
The natural and human-caused factors
of extremely low numbers of plants and
a highly restricted soil substrate and
geographic range, fragmented habitat
and low genetic diversity, effects of
drought and climate change, and lack of
proven methods for propagation and
reintroduction (as discussed under
Factor E) present an ongoing and
moderate threat to Penstemon debilis
across the entire range of the species.
These threats in themselves are not
likely to cause the species to become
endangered, but they affect the species’
ability to withstand and recover from
the effects of the threats described under
Factor A, and thus make Penstemon
debilis likely to become endangered
within the foreseeable future.
On the basis of the best available
information, we are listing Penstemon
debilis as a threatened species.
Threatened status reflects the
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vulnerability of this species to factors
that negatively affect the species and its
limited and restricted habitat. While not
in immediate danger of extinction, P.
debilis is likely to become an
endangered species within the
foreseeable future, depending on
whether energy development escalates,
draft management plans are
implemented, and current conservation
agreements are continued.
Phacelia submutica
The destruction, modification, and
fragmentation of habitat pose moderate
threats to Phacelia submutica
throughout its range. Natural gas
production with associated expansion of
pipelines, roads, and utilities;
development within the Westwide
Energy Corridor; increased access to the
habitat by ORVs; and soil and seed
disturbance by livestock, wildlife and
ORVs all threaten the species’ habitat
(as discussed under Factor A). These
ongoing and potential threats are likely
to cause P. submutica to become
endangered within the foreseeable
future, depending mainly on the rate of
energy development.
The existing regulatory mechanisms
do not address the threats to the species
or its habitat. The absence of regulatory
mechanisms exacerbates the threats
discussed under Factor A. Local or State
regulations provide no protection for the
species and its habitat. Existing Federal
regulatory mechanisms are only
partially effective at ameliorating threats
to plants and their habitat (as discussed
under Factor A).
Other natural or manmade factors
affecting the continued existence of
Phacelia submutica include the species’
small geographic range, highly specific
soil and germination requirements,
limited seed dispersal, fragmented
habitat, prolonged seed dormancy, and
potential seed bank depletion by
prolonged drought (as discussed under
Factor E). These factors make the
species vulnerable to climate change
and to the threats under Factor A (as
described above), to an extent that the
species may become endangered within
the foreseeable future, depending
primarily on the rate of future energy
development.
On the basis of the best available
information, we are listing Phacelia
submutica as a threatened species.
Threatened status reflects the
vulnerability of this species to factors
that negatively affect the species and its
limited and restricted habitat. While not
in immediate danger of extinction, P.
submutica is likely to become an
endangered species within the
foreseeable future if habitat is lost and
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existing seed banks cannot expand to
maintain the species’ range.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness and conservation by
Federal, State, and local agencies;
private organizations; and individuals.
The Act encourages cooperation with
the States and requires that recovery
actions be carried out for all listed
species. The protection measures
required of Federal agencies and the
prohibitions against certain activities
are discussed, in part, below.
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as endangered or
threatened and with respect to its
critical habitat, if any is designated.
Regulations implementing this
interagency cooperation provision of the
Act are codified at 50 CFR part 402.
Section 7(a)(4) of the Act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2) of
the Act requires Federal agencies to
ensure that activities they authorize,
fund, or carry out are not likely to
jeopardize the continued existence of
the species or destroy or adversely
modify its critical habitat. If a Federal
action may affect a listed species or its
critical habitat, the responsible Federal
agency must enter into formal
consultation with the Service.
Federal agency actions within the
habitat of these three species that may
require conference or consultation or
both as described in the preceding
paragraph include the following:
• Management, leasing, permitting,
and other actions that result in
landscape altering activities on Federal
lands administered by the BLM and
USFS;
• Issuance of section 404 Clean Water
Act (33 U.S.C. 1251 et seq.) permits by
the U.S. Army Corps of Engineers;
• Construction and management of
gas pipeline and power line ROWs by
the Federal Energy Regulatory
Commission and BLM;
• Construction and maintenance of
roads or highways by the Federal
Highway Administration; and
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• Provision of Federal funds to State
and private entities through Federal
programs such as CDOT highway
construction or improvement projects,
Housing and Urban Development Tax
Credit Assistance Program, the Service’s
Landowner Incentive Program, and the
NRCS.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to endangered plants. All prohibitions
of section 9(a)(2) of the Act,
implemented by 50 CFR 17.61, apply.
These prohibitions, in part, make it
illegal for any person subject to the
jurisdiction of the United States to
import or export, transport in interstate
or foreign commerce in the course of a
commercial activity, sell or offer for sale
in interstate or foreign commerce, or
remove and reduce the species to
possession from areas under Federal
jurisdiction. In addition, for plants
listed as endangered, the Act prohibits
the malicious damage or destruction on
areas under Federal jurisdiction and the
removal, cutting, digging up, or
damaging or destroying of such plants
in knowing violation of any State law or
regulation, including State criminal
trespass law. It also is unlawful to
violate any regulation pertaining to
plant species listed as threatened or
endangered (section 9(a)(2)(E) of the
Act). Certain exceptions to the
prohibitions apply to agents of the
Service and State conservation agencies.
No State regulations protect rare plant
species in Colorado.
We may issue permits to carry out
otherwise prohibited activities
involving endangered and threatened
plant species under certain
circumstances. Regulations governing
permits are codified at 50 CFR 17.62 for
endangered plants, and at 17.72 for
threatened plants. With regard to
endangered plants, a permit must be
issued for the following purposes: for
scientific purposes or to enhance the
propagation or survival of the species.
Regulations at 50 CFR 402.16 require
Federal agencies to reinitiate
consultation on previously reviewed
actions in instances where we have
listed a new species or subsequently
designated critical habitat that may be
affected and the Federal agency has
retained discretionary involvement or
control over the action (or the agency’s
discretionary involvement or control is
authorized by law). Consequently,
Federal agencies may sometimes need to
request reinitiation of consultation with
us on actions for which formal
consultation has been completed, if
those actions with discretionary
involvement or control may affect
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Federal Register / Vol. 76, No. 144 / Wednesday, July 27, 2011 / Rules and Regulations
subsequently listed species or
designated critical habitat.
Required Determinations
Paperwork Reduction Act of 1995
This rule does not contain any new
collections of information that require
approval by Office of Management and
Budget under the Paperwork Reduction
Act of 1995 (44 U.S.C. 3501 et seq.).
This rule will not impose recordkeeping
or reporting requirements on State or
local governments, individuals,
businesses, or organizations. An agency
may not conduct or sponsor, and a
person is not required to respond to, a
collection of information unless it
displays a currently valid Office of
Management and Budget control
number.
National Environmental Policy Act of
1969 (42 U.S.C. 4321 et seq.), need not
be prepared in connection with
regulations adopted under section 4(a)
of the Act. We published a notice
outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
recordkeeping requirements,
Transportation.
References Cited
A complete list of all references cited
is available on the Internet at https://
www.regulations.gov and upon request
from the Field Supervisor, Western
Colorado Ecological Services Field
Office (see ADDRESSES section).
PART 17—[AMENDED]
Regulation Promulgation
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as set forth
below:
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Pub. L. 99–
625, 100 Stat. 3500; unless otherwise noted.
We have determined that
Environmental Assessments and
Environmental Impact Statements as
defined under the authority of the
■
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
National Environmental Policy Act
Authors
The primary authors of this document
are staff members of the Western
Colorado Ecological Services Field
Office, U.S. Fish and Wildlife Service
(see ADDRESSES section).
§ 17.12
Species
2. Amend § 17.12(h) by adding entries
for Ipomopsis polyantha, Penstemon
debilis, and Phacelia submutica under
FLOWERING PLANTS in the List of
Endangered and Threatened Plants, to
read as follows:
Endangered and threatened plants.
*
*
*
(h) * * *
Status
*
When
listed
*
Historic
range
Family
Common name
*
Ipomopsis polyantha
*
Pagosa skyrocket ...
*
U.S.A (CO) .............
*
Polemoniaceae .......
*
E
*
....................
NA
*
Penstemon debilis ...
*
Parachute
beardtongue.
*
U.S.A. (CO) ............
*
Plantaginaceae .......
*
T
*
....................
NA
*
Phacelia submutica
*
DeBeque phacelia ..
*
U.S.A. (CO) ............
*
Hydrophyllaceae .....
*
T
*
....................
NA
Scientific name
Critical
habitat
Special
rules
FLOWERING PLANTS
*
*
*
*
*
*
*
*
*
*
Dated: July 5, 2011.
Daniel M. Ashe,
Director, Fish and Wildlife Service.
*
[FR Doc. 2011–18429 Filed 7–26–11; 8:45 am]
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*
NA
*
NA
*
NA
*
Agencies
[Federal Register Volume 76, Number 144 (Wednesday, July 27, 2011)]
[Rules and Regulations]
[Pages 45054-45075]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-18429]
[[Page 45053]]
Vol. 76
Wednesday,
No. 144
July 27, 2011
Part III
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
-----------------------------------------------------------------------
50 CFR Part 17
Endangered and Threatened Wildlife and Plants; Determination of
Endangered Status for Ipomopsis polyantha (Pagosa Skyrocket) and
Threatened Status for Penstemon debilis (Parachute Beardtongue) and
Phacelia submutica (DeBeque Phacelia); Final Rule
Federal Register / Vol. 76 , No. 144 / Wednesday, July 27, 2011 /
Rules and Regulations
[[Page 45054]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R6-ES-2010-0015; MO 92210-0-0008 B2]
RIN 1018--AV83
Endangered and Threatened Wildlife and Plants; Determination of
Endangered Status for Ipomopsis polyantha (Pagosa Skyrocket) and
Threatened Status for Penstemon debilis (Parachute Beardtongue) and
Phacelia submutica (DeBeque Phacelia)
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), determine
endangered status for Ipomopsis polyantha (Pagosa skyrocket), a plant
species in Archuleta County, Colorado; threatened status for Penstemon
debilis (Parachute beardtongue) in Garfield County, Colorado; and
threatened status for Phacelia submutica (DeBeque phacelia) in Mesa and
Garfield Counties, Colorado, under the Endangered Species Act of 1973,
as amended (Act). Designation of critical habitat for the three species
is proposed concurrently in a separate rule in this edition of the
Federal Register.
DATES: This rule becomes effective on August 26, 2011.
ADDRESSES: This final rule is available on the Internet at https://www.regulations.gov. Comments and materials received, as well as
supporting documentation used in preparing this final rule are
available for public inspection, by appointment, during normal business
hours, at U.S. Fish and Wildlife Service, Western Colorado Ecological
Services Field Office, 764 Horizon Drive, Building B, Grand Junction,
CO 81506-3946; telephone 970-243-2778; facsimile 970-245-6933.
FOR FURTHER INFORMATION CONTACT: Al Pfister, Western Colorado
Supervisor, U.S. Fish and Wildlife Service, Ecological Services Field
Office, 764 Horizon Drive, Building B, Grand Junction, CO 81506-3946;
telephone 970-243-2778, extension 29; facsimile 970-245-6933. If you
use a telecommunications device for the deaf (TDD), call the Federal
Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Previous Federal Actions
Ipomopsis polyantha
We first identified Ipomopsis polyantha as a taxon under review in
the 1983 Supplement to Review of Plant Taxa for Listing as Endangered
or Threatened Species (48 FR 53640, November 28, 1983). In that
document, we included the species as a Category 2 candidate, based on
our evaluation at that time. We published our decision to discontinue
candidate categories and to restrict candidate status to those taxa for
which we had sufficient information to support issuance of a proposed
rule on December 5, 1996 (61 FR 64481). This resulted in the deletion
of Ipomopsis polyantha from the list of candidate taxa for listing. We
added the species to the list of candidates again in the 2005 Candidate
Notice of Review (CNOR) (70 FR 24870, May 11, 2005) with a listing
priority number (LPN) of 2. A listing priority of 2 reflects threats
that are imminent and high in magnitude, as well as the taxonomic
classification of I. polyantha as a full species. We published a
complete description of our listing priority system in the Federal
Register (48 FR 43098, September 21, 1983).
On June 23, 2010, we proposed to list Ipomopsis polyantha as
endangered (75 FR 35721). In the proposed rule, we found that critical
habitat for the species was prudent, but not determinable at that time.
A proposed rule to designate critical habitat for this species is being
published concurrently with this final rule.
Penstemon debilis
We first included Penstemon debilis as a category 2 candidate
species in the February 21, 1990, Review of Plant Taxa for Listing as
Endangered or Threatened Species (55 FR 6184). When we abandoned the
use of numerical category designations in 1996, we changed the status
of P. debilis to a candidate under the current definition. We published
four CNOR lists between 1996 and 2004, and P. debilis remained a
candidate species with an LPN of 5 on each (62 FR 49398, September 19,
1997; 64 FR 57534, October 25, 1999; 66 FR 54808, October 30, 2001; 67
FR 40657, June 13, 2002). An LPN of 5 is assigned to species with non-
imminent threats of a high magnitude.
In the 2005 CNOR (70 FR 24870, May 11, 2005), we changed the LPN
for Penstemon debilis from 5 to 2 based on an increase in the intensity
of energy exploration along the Roan Plateau escarpment, making the
threats to the species imminent. The CNOR lists published in 2006,
2007, and 2008 maintained P. debilis as a candidate species with an LPN
of 2 (71 FR 53756, September 12, 2006; 72 FR 69034, December 6, 2007;
73 FR 75176, December 10, 2008).
In each assessment since its recognition as a candidate species in
1996, we determined that publication of a proposed rule to list the
species was precluded by our work on higher priority listing actions.
In 2008, we received funding to initiate the proposal to list Penstemon
debilis. In the 2008 notice, we announced that we had not updated our
assessment for this species, as we were developing a proposed listing
rule (73 FR 75227). On June 23, 2010, we proposed to list P. debilis as
threatened (75 FR 35721). In the proposed rule, we found that critical
habitat for the species was prudent, but not determinable at that time.
A proposed rule to designate critical habitat for this species is being
published concurrently with this final rule.
Phacelia submutica
We included Phacelia submutica as a category 1 candidate species in
the 1980 Review of Plant Taxa for Listing as Endangered or Threatened
Species (45 FR 82480, December 15, 1980). In that notice, category 1
candidates were defined as species for which the Service had
``sufficient information on hand to support the biological
appropriateness of their being listed as Endangered or Threatened
species.'' We changed the candidate status of P. submutica to category
2 on November 28, 1983 (48 FR 53640). On February 21, 1990, we again
identified P. submutica as a category 1 candidate species (55 FR 6184).
In the February 28, 1996, Federal Register (61 FR 7596), all category 1
candidate species became candidates under the current definition. We
assigned P. submutica an LPN of 11. In the 2005 CNOR (70 FR 24870, May
11, 2005) we raised the LPN to 8, to reflect the increasing level of
threats, which were imminent and of moderate magnitude.
On May 11, 2004, we received a petition from the Center for
Biological Diversity (CBD) to list, as endangered, 225 species we
previously had identified as candidates for listing, including Phacelia
submutica (CBD 2004, p. 146). Under requirements in section 4(b)(3)(B)
of the Act (16 U.S.C. 1531 et seq.), the CNOR and the Notice of
Findings on Resubmitted Petitions published by the Service on May 11,
2005 (70 FR 24870), included a finding that the immediate issuance of a
proposed listing rule and the timely promulgation of a final rule for
each of these petitioned species, including P.
[[Page 45055]]
submutica, was warranted but precluded by higher priority listing
actions, and that expeditious progress was being made to add qualified
species to the lists.
On April 28, 2005, the Center for Native Ecosystems (CNE), the
Colorado Native Plant Society, and botanist Steve O'Kane, Jr., Ph.D.,
submitted a petition to the Service to list Phacelia submutica as
endangered or threatened within its known historical range, and to
designate critical habitat concurrent with the listing (CNE et al.
2005, p. 1). We considered the information in the petition when we
prepared the 2006 CNOR (71 FR 53756, September 12, 2006). Section
4(b)(3)(C) of the Act requires that when we make a warranted but
precluded finding on a petition, we are to treat such a petition as one
that is resubmitted on the date of such a finding. We identified P.
submutica as a species for which we made a continued warranted but
precluded finding on a resubmitted petition in the Federal Register on
December 6, 2007 (72 FR 69034), December 10, 2008 (73 FR 75176), and
November 9, 2009 (74 FR 57804). We retained an LPN of 8 for the
species. In the 2008 CNOR, we announced that we had not updated our
assessment for this species, as we were developing a proposed listing
rule (73 FR 75227). On June 23, 2010, we proposed to list P. submutica
as threatened (75 FR 35721). In the proposed rule, we found that
critical habitat for the species was prudent, but not determinable at
that time. A proposed rule to designate critical habitat for this
species is being published concurrently with this final rule.
Summary of Comments and Recommendations
We requested written comments from the public on the proposed
listing of Ipomopsis polyantha, Penstemon debilis, and Phacelia
submutica during the comment period associated with the publication of
the proposed rule (75 FR 35721), which opened on June 23, 2010, and
closed on August 23, 2010. We did not receive any requests for a public
hearing. We also contacted appropriate Federal, State, and local
agencies; scientific organizations; and other interested parties and
invited them to comment on the proposed rule during this comment
period.
During the comment period, we received 13 comment letters
addressing the proposed rule. All substantive information provided
during the comment period has either been incorporated directly into
this final determination or is addressed below.
Peer Review
In accordance with our peer review policy published on July 1, 1994
(59 FR 34270), we solicited expert opinions from three knowledgeable
individuals with scientific expertise that included familiarity with
the species, the habitats in which the species occur, and conservation
biology principles. We received responses from the three peer
reviewers.
We reviewed all comments received from the peer reviewers for
substantive issues and new information regarding the proposed listing
of Ipomopsis polyantha, Penstemon debilis, and Phacelia submutica. The
peer reviewers concurred with our analysis and conclusions, and
provided additional information, clarifications, and suggestions to
improve the final rule. Peer reviewer comments are addressed in the
following summary and incorporated into the final rule as appropriate.
Peer Reviewer Comments
(1) Comment: One peer reviewer said that population trends cannot
be identified from available data for Penstemon debilis and Phacelia
submutica, but noted that annual fluctuations in plant numbers for both
species make them vulnerable to additional stressors such as habitat
loss. Another reviewer said that the lowest total annual plant count
for P. submutica should be zero, because the plants do not emerge at
all during very dry years. An agency commenter was concerned that the
zero counts might reflect inadequate survey methods.
Our Response: The low and high plant counts reported for Phacelia
submutica are simply a record of the lowest and highest plant counts
recorded during blooming season surveys at known occupied sites. Not
all occurrences are visited every year. Zero counts are reported only
when a site was visited, not as a default. We report the negative
surveys to show that the plants really do not emerge during some years,
and that the fluctuations in plant numbers make it hard to measure the
population trend.
(2) Comment: One peer reviewer indicated the correct name for the
sensitive species of blazing star associated with Penstemon debilis is
Mentzelia rhizomata (Roan Cliffs blazingstar), not Mentzelia argillosa
(Arapien blazingstar).
Our Response: We corrected the text in this final rule accordingly.
This is an important distinction, because Mentzelia rhizomata is a
Bureau of Land Management (BLM) sensitive species that will benefit
from protection of P. debilis habitat because it only grows on the same
layers of shale.
(3) Comment: One peer reviewer stated that the extent and imminent
nature of energy development may not have been ameliorated to the
extent suggested in the proposed rule. In 2010, natural gas production
in the range of Phacelia submutica and Penstemon debilis was the
highest in Colorado, an increase from the 2008 report that was cited in
the proposal.
Our Response: We have updated this final rule with the natural gas
production reports provided by the reviewer and the Colorado Oil and
Gas Conservation Commission (2010, pp. 1-2).
(4) Comment: One peer reviewer stated the potential impact of
climate change on Penstemon debilis may be greater than indicated in
the proposal, because the species is restricted to only one layer of
shale; thus, it may be impossible for this species to migrate to a more
suitable climate space if the substrate it depends upon does not exist.
The peer reviewer indicated that Camille Parmesan (2006, p. 649) has
authored a more comprehensive and current review documenting species'
distributional shifts in response to warming.
Our Response: We have incorporated Parmesan's findings into our
analysis of Factor E for Penstemon debilis. However, the current data
are not reliable enough at the local level for us to draw conclusions
regarding the imminence of climate change threats to P. debilis or the
other two species.
(5) Comment: One peer reviewer suggested the potential impacts of
fugitive dust on Penstemon debilis are overstated in the proposed rule.
For at least the viable population on public land, the nature of the
road is prohibitive to vehicles moving at speeds that could generate
much dust. Phacelia submutica, which is more exposed to dust, should
have an evaluation of dust impacts because it occupies habitat in the
vicinity of roads that can better accommodate heavy, fast moving
traffic. Additionally, Phacelia submutica habitats are more likely to
be in the vicinity of well pads and pipelines than Penstemon debilis,
and thus inclusion of an evaluation of the threat from dust on this
species is warranted.
Our Response: We consider dust effects an impact that does not rise
to the level of a threat to Penstemon debilis or Phacelia submutica,
because we do not have research results to assess its effect. However,
we have observed heavy dust settling on at least three of the Penstemon
debilis occurrences from
[[Page 45056]]
heavy equipment and truck traffic (Ewing 2009a, p. 3). Most Phacelia
submutica occurrences are not close to dust-producing roads, but
Service biologists have observed dust sources along a pipeline
construction route near Phacelia submutica occurrences.
(6) Comment: One peer reviewer stated the proposed listing rule
fails to include pollinator information for Phacelia submutica and the
potential for disruption of pollinator-plant interactions due to
climate variations.
Our Response: The pollination mechanism for Phacelia submutica
remains unknown at this time. Based on the size and shape of the
flowers and lack of insects observed on the flowers, we expect that P.
submutica is self-pollinated. We have initiated a pollination study for
this species, but the results are not yet available. If the species did
depend on pollinators for reproduction, then climate change could
disrupt this relationship because the plants are receptive for a very
short time. Pollination could fail to occur if the weather factors
allowing the pollinating insects to emerge were not synchronized with
plant receptivity. Because we have no data to indicate that pollinators
are required, we do not assess the effects of climate variations on
pollinator-plant interactions.
(7) Comment: One peer reviewer indicated that critical habitat
should be determined for these three species based on the information
available at this time. Given the level of threats and the narrow
distribution of all three species, it is essential to provide the
protection of designated critical habitat as soon as possible.
Our Response: We are proposing to designate critical habitat for
the three species concurrently with this final rule. That proposal is
published elsewhere in today's Federal Register. Comments on the
proposal will be accepted following publication.
(8) Comment: Peer reviewers and commenters pointed out an error on
page 35733 of the proposed listing rule, where the projected average
temperature warming per decade was correctly cited as 0.2 [deg]C, but
the equivalent was incorrectly shown as 32.4 [deg]F.
Our Response: For the next 2 decades, a warming of about 0.36
[deg]F (0.2 [deg]C) per decade is projected. By the end of the 21st
century, average global temperatures are expected to increase 1.08 to
7.2 [deg]F (0.6 to 4 [deg]C) (Intergovernmental Panel on Climate Change
(IPCC) 2007, p. 45). We corrected the text in this final rule
accordingly.
Comments From the State of Colorado
Section 4(i) of the Act states, ``the Secretary shall submit to the
State agency a written justification for his failure to adopt
regulations consistent with the agency's comments or petition.''
Comments received from the State regarding the proposal to list
Ipomopsis polyantha, Penstemon debilis, and Phacelia submutica are
addressed below. The Colorado Natural Areas Program (CNAP) is the State
agency within Colorado State Parks that works to cooperatively monitor
and protect Colorado's most significant natural features, including
rare plants.
Penstemon debilis
(9) Comment: The CNAP is concerned that listing Penstemon debilis
will discourage future voluntary protections by the oil and gas
industry. The CNAP stated in its letter that Oxy USA, Inc. (Oxy), has
implemented voluntary best management practices to avoid impacts and
reduce threats to the species, and they have supported 3 years of
monitoring to document the status of the species on their land. The
CNAP stated that although monitoring results at Mount (Mt.) Callahan
and Mt. Callahan Saddle Natural Areas show a statistically
insignificant downward trend in number of plant stems per plot, this
trend may be a natural variation in population size or caused by
climatic or other environmental factors, not by any effects from the
gas well construction. No impacts to the P. debilis individuals were
observed that may be related to natural gas development in the Natural
Areas, and the buffers instituted are believed to be adequate to
protect the populations. The CNAP will continue to work with Oxy to
track the trends of this species. Monitoring will be done with care to
minimize negative impacts from trampling of individual plants by people
collecting the data.
Our Response: The Service acknowledges that Oxy has implemented
voluntary best management practices to protect two of the Penstemon
debilis occurrences on their private land. Oxy and other energy
companies are aware that their compliance with conservation measures
recommended by the Service is entirely voluntary. We believe that this
level of protection, while voluntary and non-binding, minimizes the
threats to the species to an extent that we can list it as threatened,
rather than endangered. We also must consider the cumulative threats to
the species as a whole throughout its entire limited range in making
our listing decision. Despite the positive conservation being
implemented by Oxy, we determined that the species still meets the
definition of a threatened species because of cumulative effects of a
variety of threats, many not under the control of Oxy, and the threats
present in the remainder of the species' range.
Phacelia submutica
(10) Comment: The CNAP believes that the greatest threat to
Phacelia submutica is oil and gas development that may be allowed
within occupied habitat under current Federal regulations, because some
surveys in potential habitat may not indicate the presence of this
ephemeral and inconsistent species. Because this species may not emerge
on an annual basis, that makes potential surveys for it very
challenging, and surveys could result in the unintentional leasing and
development of occupied habitat.
Our Response: Our threats analysis incorporates and supports CNAP's
statement regarding the primary threats to Phacelia submutica.
Federal Agency Comments
Penstemon debilis
(11) Comment: In response to our description in the proposed rule
of impacts that resulted from inadequate regulation, the BLM pointed
out that the Anvil Points Mine reclamation was a Superfund project that
was not subject to the Act, and that section 7 consultation was not
required for the communication site access because the species was only
a candidate for listing. Of the 88 plants at the reclamation site that
were transplanted, covered, or fenced, BLM reported 71 survivors at the
end of the 2009 growing season.
Our Response: The BLM avoided and minimized impacts from the
reclamation project voluntarily, with input from the Service that was
comparable to a section 7 consultation. However, plants were destroyed,
habitat was modified, and the ongoing issue of impacts due to
communication site access remains unresolved. We believe that listing
as a threatened species will provide more support for agency efforts to
protect the species.
Phacelia submutica
(12) Comment: The U.S. Forest Service (USFS) feels that critical
habitat should not be designated for Phacelia submutica at this time
because we do not have enough information about its specific soil
requirements, seed bank, reproductive biology, or minimum population
size; and that new populations being discovered each year are leading
to new concepts of the species' distribution and requirements.
[[Page 45057]]
Our Response: Designation of critical habitat for the three species
is proposed concurrently in a separate rule in this edition of the
Federal Register. The criteria for critical habitat were evaluated
using the best scientific and commercial data available. Surveys in
2009-2010 increased the known sites and numbers of plants, but did not
change the habitat description or extend the range boundaries. We
believe that Phacelia submutica has a large enough range, enough
populations, and enough individuals that the occupied habitat alone, if
protected from threats, would be adequate for the future survival and
recovery of the species. We recognize that critical habitat designated
at a particular point in time may not include all of the habitat areas
that we may later determine are necessary for the recovery of the
species. A critical habitat designation does not signal that habitat
outside the designated area is unimportant or may not be required for
recovery of the species.
Public Comments
(13) Comment: Support for listing the three plants was received
from the Colorado Natural Heritage Program (CNHP), seven other non-
profit environmental organizations in Colorado, and one local resident.
Some of these commenters also believe that the species proposed for
listing as threatened should not be subject to a 4(d) rule, which is a
special regulation that can provide greater flexibility by allowing
actions prohibited under section 9(a)(1) of the Act for species listed
as threatened.
Our Response: We believe that the general prohibitions for
threatened plants at 50 CFR 17.71 are appropriate for these two plant
species. As a result, we did not develop a 4(d) rule for Penstemon
debilis or Phacelia submutica, the two species we are listing as
threatened.
(14) Comment: Several environmental groups commented that critical
habitat is both prudent and determinable for all three species, and it
should include all known occurrences of each species, including
historical and recently extirpated and nonviable, as well as potential
habitat.
Our Response: We are proposing critical habitat for each of the
three species concurrently with this final listing rule. Critical
habitat is defined in section 3 of the Act as: (1) The specific areas
within the geographical area occupied by the species, at the time it is
listed in accordance with the Act, on which are found those physical or
biological features that are essential to the conservation of the
species, and which may require special management considerations or
protection; and (2) Specific areas outside the geographical area
occupied by the species at the time it is listed, upon a determination
that such areas are essential for the conservation of the species. All
known occurrences are evaluated, and must meet the criteria to be
included in proposed critical habitat.
Penstemon debilis
(15) Comment: Andrea Wolfe shared her unpublished results of
genetic research on Penstemon debilis in 2009, which show that its
genetic diversity is very limited and each occurrence is genetically
separated from the others, which indicates inbreeding depression.
Our Response: We appreciate receiving these results, which indicate
the limited ability of Penstemon debilis to adapt to habitat or climate
changes. We included them in our assessment of other natural factors
affecting the species, under Factor E.
Summary of Changes From Proposed Rule
No substantial changes have been made in the threats analysis or
determinations for the three species. Field surveys in 2010 increased
the recorded number of plants for each species, but did not expand
their known ranges or any decrease in the level of threats.
Endangered Status for Ipomopsis polyantha; Threatened Status for
Penstemon debilis and Phacelia submutica
Background
It is our intent to discuss below only those topics directly
relevant to the listing of Ipomopsis polyantha as endangered, and
Penstemon debilis and Phacelia submutica as threatened, in this section
of the final rule. More information on these species is available in
the June 23, 2010, proposed rule (75 FR 35721).
Species Information--Ipomopsis polyantha
Taxonomy and Species Description
Ipomopsis polyantha is a rare plant endemic to shale outcrops in
and around the Town of Pagosa Springs in Archuleta County, Colorado.
The species is in the Polemoniaceae (phlox) family and was originally
described by Rydberg (1904, p. 634) as Gilia polyantha. Two varieties,
G. polyantha var. brachysiphon and G. polyantha var. whitingii, were
recognized by Kearney and Peebles (1943, p. 59). Grant (1956, p. 353)
moved the species into the genus Ipomopsis. Currently available
information indicates that I. polyantha is a distinct species (Porter
and Johnson 2000, p. 76; Porter et al. 2010, pp. 195, 196, 199). It is
treated as such in the PLANTS database (U.S. Department of Agriculture,
Natural Resource Conservation Service (NRCS) 2003), and in the
Integrated Taxonomic Information System (2001). Reports of this species
occurring in Arizona and New Mexico by the PLANTS National Database and
State floras actually pertain to the two species that were formerly
treated as varieties of Ipomopsis polyantha (Anderson 2004, pp. 11,
15).
The CNHP ranks Ipomopsis polyantha as critically imperiled globally
(G1) and in the State of Colorado (S1) (CNHP 2010b, pp. 1-5). The
Nature Conservancy (TNC) and CNHP also developed a scorecard that ranks
I. polyantha among the most threatened species in the State based on
number of plants, quality of the plants and habitat, threats, and
adequacy of protection (CNHP and TNC 2008, p. 102).
Ipomopsis polyantha is an herbaceous biennial 12 to 24 inches (in)
(30 to 60 centimeters (cm)) tall, branched from near the base above the
basal rosette of leaves. Deeply divided leaves with linear segments are
scattered up the stem. Stems and flower clusters are covered with
glandular hairs. Flower clusters are along the stem in the axils of the
leaves as well as at the top of the stem. The white flowers are 0.4 in
(1 cm) long, with short corolla tubes 0.18 to 0.26 in (0.45 to 0.65 cm)
long, and flaring corolla lobes flecked with purple dots (Anderson
1988, p. 3). These dots are often so dense that they give the flower a
pinkish or purplish hue. The stamens extend noticeably beyond the
flower tube, and the pollen is blue (Grant 1956, p. 353), changing to
yellow as it matures (Collins 1995, p. 34). Seeds form a mucilaginous
(secreting sticky mucous) coat after they are wet. Seeds germinate much
faster in Mancos Shale soil than in potting soil (Collins 1995, p. 72).
Mature seeds germinate to form rosettes that produce flowering stalks
during the next growing season, or they may persist as rosettes for a
year or more until conditions are right for flowering. Plants produce
abundant fruits and seeds, but have no known mechanism for long-
distance dispersal (Collins 1995, pp. 111-112). After seeds are mature,
the plants dry up and die. We do not know how long the seeds remain
viable.
Pollination by bees is the most common means of reproduction for
Ipomopsis polyantha, and the primary pollinators are the honey bee
(Apis
[[Page 45058]]
mellifera), metallic green bee (Augochlorella spp.), bumble bee (Bombus
spp.), and digger bee (Anthophora spp.) (Collins 1995, pp. 71-72).
Ipomopsis polyantha is limited to Pagosa-Winifred soils derived
from Mancos Shale. The soil pH is nearly neutral to slightly alkaline
(6.6 to 8.4). The elevation range is 6,750 to 7,775 feet (ft) (2,050 to
2,370 meters (m)) (Service 2011c, p. 1). Plants occur in discontinuous
colonies as a pioneer species on open shale or as a climax species
along the edge of Pinus ponderosa (Ponderosa pine), mixed P. ponderosa
and Juniperus scopulorum (Rocky mountain juniper), or Juniperus.
osteosperma (Utah juniper) and Quercus gambellii (Gambel oak) forested
areas. In 1988, Anderson (p. 7) reported finding the highest densities
under P. ponderosa forests with montane grassland understory. Now the
species is found mostly on sites that are infrequently disturbed by
grazing, such as road right-of-ways (ROWs) that are fenced from grazing
(as opposed to open range), lightly grazed pastures, and undeveloped
lots (Anderson 2004, p. 20).
The two known occurrences of Ipomopsis polyantha are within about
13 miles (mi) (21 kilometers (km)) of each other, and collectively
occupy about 388.4 acres (ac) (157.1 hectares (ha)) of habitat within a
range that includes about 6.5 square mi (16.8 square km). The Pagosa
Springs occurrence is southeast of the Town of Pagosa Springs along
both sides of U.S. 84. Occupied habitat extends southward on the
highway ROW for 3 mi (4.8 km) from the intersection with U.S. 160, and
on private lands on both sides of the highway. The Dyke occurrence is
about 10 mi (16 km) west of Pagosa Springs along U.S. Highway 160. It
includes 0.5 mi (0.8 km) of highway ROW on both sides of U.S. 160,
adjacent private land, and a BLM parcel. Species occurrences are
further described in the June 23, 2010, proposed rule to list the
species (75 FR 35721). Table 1 summarizes land ownership and results of
the most recent plant counts reported within the two I. polyantha
occurrences.
Table 1--Occupied Habitat for Ipomopsis polyantha by Landownership (acres (ac) (hectares (ha))
[Lyon 2006a; CNAP 2007; CNAP 2008, pp. 1-5; CNHP 2008a; CNHP 2010a, pp. 1-8; Service 2011a, p. 2; Service 2011b,
p. 1]
----------------------------------------------------------------------------------------------------------------
Occurrence Land ownership ac (ha) Flowering Rosettes
----------------------------------------------------------------------------------------------------------------
Pagosa Springs including Mill Creek State ROW............ 27.6 (11.2) 3,029 3,083
County ROW........... 5.5 (2.2) 469 403
Town of Pagosa 7.5 (3.0) 126 15
Springs.
Private.............. 301.7 (122.1) 158,326 174,989
----------------------------------------------------------------------------------------------------------------
Subtotals...................... ..................... 342.3 (138.5) 161,950 178,490
============================================================================
Dyke............................... State ROW............ 2.3 (0.9) 19 102
BLM.................. 9.9 (4.0) 88 164
Private.............. 33.9 (13.7) 163 275
----------------------------------------------------------------------------
Subtotals...................... ..................... 46.1 (18.6) 270 541
----------------------------------------------------------------------------------------------------------------
Totals..................... ..................... 388.4 (157.1) 162,220 179,031
----------------------------------------------------------------------------------------------------------------
Approximately 2.5 percent of the occupied habitat is on Federally
managed BLM land, 9.1 percent on State and County highway ROWs, 86.4
percent on private lands, and 1.9 percent on Pagosa Springs town park
land and county land (Service 2011a, p. 2).
In 2004, the total estimate of flowering plants throughout the
entire range of the species was 2,246 to 10,526 (Anderson 2004, p. 40).
Plant surveys from 2005 to 2007 documented dramatic increases in the
number of flowering individuals and rosettes within the Pagosa Springs
occurrence at two sites on private land and on the U.S. 84 ROW (CNAP
2007, pp. 1-2). This increase was primarily attributed to the plants
surveyed in 2005 and 2006 on a 3-ac (1.2-ha) private land site in the
Pagosa Springs occurrence. The rapid appearance of such a dense patch
of plants illustrates the species' ability to colonize barren Mancos
Shale soil, and demonstrates the reproductive success of the species;
however, the sites where they grow are vulnerable to habitat
destruction. Currently, the total estimate of flowering plants is
162,220 (see Table 1 above). Again, the increase from 2,426 flowering
plants counted in 2004 was largely due to the discovery of previously
undocumented plants during new surveys on private lands. The trend in
the species' status since 1988 is one of fluctuating population size
that is typical of biennial species, combined with the loss of several
hundred plants due to development (see Factor A below).
Summary of Factors Affecting Ipomopsis polyantha
Section 4 of the Act and its implementing regulations (50 CFR 424)
set forth the procedures for adding species to the Federal Lists of
Endangered and Threatened Wildlife and Plants. A species may be
determined to be an endangered or threatened species due to one or more
of the five factors described in section 4(a)(1) of the Act: (A) The
present or threatened destruction, modification, or curtailment of its
habitat or range; (B) overutilization for commercial, recreational,
scientific, or educational purposes; (C) disease or predation; (D) the
inadequacy of existing regulatory mechanisms; or (E) other natural or
manmade factors affecting its continued existence. Listing actions may
be warranted based on any of the above threat factors, singly or in
combination. Each of these factors is discussed below.
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
Ipomopsis polyantha is threatened with destruction of plants and
habitat due to commercial, residential, municipal, and agricultural
property development, and associated new utility installations and
access roads. We have documented recent losses of habitat and
individuals within the Pagosa Springs and Dyke occurrences of the
species, as described in more detail below.
Land Use Changes
Primary land use within the range of Ipomopsis polyantha has
historically
[[Page 45059]]
been livestock (horses or cattle) grazing, with homes on parcels of 35
ac (14 ha) or more. Several small businesses now occur along U.S. 84
within the Pagosa Springs occurrence. The intersection of U.S. 160 and
U.S. 84 is zoned by the Town of Pagosa Springs for business, and
commercially zoned land is currently available for development.
Archuleta County also is considering sites in this area for new county
buildings. These current and potential conversions of agricultural
lands to residential and commercial development are incompatible with
conservation of I. polyantha in the long term because the conversions
cause direct mortality and permanent loss of habitat. Conversely,
habitat modified by grazing may be recovered by changes in management.
Residential development is increasing in Archuleta County. The
population of Archuleta County was 5,000 in 1990, increasing to 12,430
in 2009 (U.S. Census Bureau 2011). Prior to the slowing down of the
real estate market over the past few years, projections for new
development in Archuleta County were high. For example, all private
land across the entire range of Ipomopsis polyantha is scheduled for
development in the Archuleta County and Town of Pagosa Springs
Community Plan (2000). In this plan, all areas occupied by I. polyantha
on private land outside of the Town limits are planned for low (35 ac
(14 ha)), medium (3 to 35 ac (1.2 to 14 ha)), or high (2 to 5 ac (0.81
to 2 ha)) density housing. The rate of current and proposed development
is the most significant threat to the species, because development
planned for the next 5 to 10 years will likely impact 86 percent of the
species' habitat. This rate of land conversion puts the species at risk
of extinction.
Private Development of 35 Acres (14 Hectares) or Less
Within the Pagosa Springs occurrence, a residential and
agricultural development of about a dozen 35-ac (14-ha) parcels was
built prior to 2005 on occupied habitat east of U.S. 84 (Archuleta
County Assessor 2008, p. 1). In 2005, when most residences were new,
about 782 flowering plants were counted in meadows and along the fences
and access roads (Lyon 2005, pp. 1-2). By 2008, an increased number of
horses were pastured in the meadows, roadsides and driveways were
graded or widened, and few plants or rosettes could be found as a
result (Mayo 2008b, p. 2). This information indicates that Ipomopsis
polyantha plants are vulnerable to grazing effects and road
improvements, and habitat can be modified to exclude plants in as few
as 3 years. We do not know exactly what level of grazing is sufficient
to eliminate the I. polyantha plants in a pasture. In 2006, at another
location along U.S. 84, a private landowner mowed several hundred feet
of occupied habitat on the highway ROW (Lyon 2006a, p. 1). No plants or
rosettes were found at this site from 2006 to 2008, indicating that
mowing destroys plants and halts reproduction. In 2005, dense patches
of flowering plants were noted, from across the fence, in a privately
owned meadow along U.S. 84. In 2007, a new home was built, and the
meadow was mowed; no plants could be seen at the same site in 2008
(Mayo 2008b, p. 2), again indicating that mowing destroys flowering
plants and inhibits reproduction, because the seeds cannot mature and
grow into rosettes. We do not know how long the seeds remain viable in
the soil.
Private and County Development of Large Parcels
In 2008, the Pagosa Springs Town Council approved annexation of the
96-ac (39-ha) private development called Blue Sky Village into the Town
(Aragon 2008a, pp. 1-2). The proposed development plan was for a mixed
commercial and high- to low-density residential village (Hudson 2008,
p. 1). The 96-ac (39-ha) parcel is adjacent to the highest density of
Ipomopsis polyantha plants, and includes about 2,562 ft (781 m) of
habitat on U.S. 84 frontage at the center of the species' distribution
(Archuleta County Assessor 2008, p. 1). Plants have been observed on
the property from over the fence, but not counted. Occupied habitat
also borders the southern edge of the property.
In 2010, the Blue Sky Village property went into foreclosure. The
County announced that it will acquire the property. Possible uses of
the land include county buildings, sports fields, and the sale of
commercial lots along the highway (Hudson 2010, p. 1). Development of
the Blue Sky Village/County property would significantly reduce the
amount of habitat within the species' range. Location of the
development between the highest density of plants and the rest of the
Pagosa Springs occurrence on the east side of U.S. 84 would further
fragment the habitat that has already been impacted by commercial,
residential, and agricultural land uses.
Another private development that includes 47 ac (19 ha) of occupied
habitat and about 1 mi (1.6 km) of frontage along the west side of U.S.
84, is being considered for annexation and development (Aragon 2008a,
p. 2; Archuleta County Assessor 2008, p. 1; Hudson 2010, p. 1).
Preliminary plans show home sites and open space on the 47 ac (19 ha)
of currently occupied plant habitat.
The above two development proposals would cover about 42 percent of
the habitat within the Pagosa Springs occurrence, which is the larger
of the two occurrences and is essential to the species' continued
existence. Plants and habitat along U.S. 84 ROW are likely to be
disturbed or destroyed by construction of new access roads, utility
installations, and acceleration and deceleration lanes built to
accommodate the proposed developments. The pace of development around
Pagosa Springs fluctuates with the economy, but given the direction in
the County plan and the projected growth rates for the County and the
Town of Pagosa Springs, it is highly likely that further development
will occur along U.S. 84 within 5 to 10 years.
A third large parcel of 1,362 ac (551 ha) proposed for development,
plus 2,819 ft (859 m) of U.S. 84 frontage, is another annexation to the
Town of Pagosa Springs being considered within the range of Ipomopsis
polyantha. The proposed development, called Blue Sky Ranch, would
include single and multi-family residential housing, a hotel and
conference center, a golf course with clubhouse, and an equestrian
center with riding trails and a multi-use arena (Aragon 2008b, p. 2).
The status of the proposed development is unknown at this time, because
it depends on the real estate market. This area has not been surveyed
for plants, and is not included in the total occupied habitat.
Utilities Installations and Maintenance
Utilities installations and construction activities that are
necessary for development can eliminate habitat and destroy Ipomopsis
polyantha plants. During 2005 and 2006, a sewer line installation on
the U.S. 84 ROW resulted in the loss of about 498 plants and 541
rosettes and the modification of about 1,473 ft (449 m) of roadside
habitat (Mayo 2008c, p. 8). The Colorado Department of Transportation
(CDOT) and Archuleta County consulted with the Service, and agreed on
avoidance measures for this project, but contractors failed to follow
the protocol. Where avoidance of plants and habitat was specified,
topsoil, plants, and rosettes were scraped away on the bank; where
native plant seeding was specified, nonnative grasses were seeded; and
where straw was prohibited, a thick layer of straw was
[[Page 45060]]
applied (Mayo 2008c, pp. 1-4; Peterson 2006, pp. 1-3). As a result, in
2008, the remaining 8 flowering plants and 5 rosettes at this site were
found in one spot, near plants on an adjacent property not disturbed by
the sewer line project (Mayo 2008c, p. 8). In 2010, the combined number
of flowering plants and rosettes at the site was 167. This incident
demonstrates that I. polyantha cannot quickly recover from soil
disturbance.
Although I. polyantha can colonize unvegetated Mancos Shale soil
near a seed source, the number of flowering plants that appear in
subsequent years depends on seed production and the survival of
rosettes that are not outcompeted by other species or destroyed during
ground disturbance. Power line maintenance was completed within
occupied habitat in the Pagosa Springs occurrence in 2007. As a result
of careful planning, there was negligible damage to adult plants.
However, 278 rosettes were transplanted, but did not survive to
reproduce for unknown reasons. We conclude that the species is highly
vulnerable to ground disturbance during development because seedlings
and rosettes are destroyed and transplanting is not known to be
successful.
Highway Right of Ways
The Archuleta County and Town of Pagosa Springs revised 2004 Trails
Plan (2004, p. 18) calls for an 8-ft (2.4-m) wide, 2.5-mi (4-km) long,
paved bike path on the highway ROW from U.S. 160 south along U.S. 84 in
occupied Ipomopsis polyantha habitat. This route, prioritized for
completion as soon as funding is available, would eliminate about 38
percent of the total occupied habitat on the highway ROWs and 4 percent
of the total occupied habitat for the species (see Table 1 above).
Another planned paved bike trail, parallel to U.S. 160 and through the
Dyke occurrence of I. polyantha, is on the low priority list in the
Trails Plan (Archuleta County and Town of Pagosa Springs 2004, p. 28).
Development of this bike trail would eliminate the portion of the Dyke
occurrence located on the south side of the highway where the trail
would be located, covering about 3 percent of the total highway ROW
habitat.
The distribution of Ipomopsis polyantha within highway ROWs makes
this species susceptible to threats associated with highway activities
and maintenance. Exotic grasses planted by CDOT along roadsides
dominate the ROW between pavement and ditch, limiting most I. polyantha
plants to the ROW bank between ditch and fence. This limitation to the
species' habitat along roadsides is significant because so little
habitat exists elsewhere for the species. I. polyantha plants growing
within the highway ROW along U.S. 84 in 2004 were killed when the
thistles growing among them were treated with herbicide (Anderson 2004,
p. 36). Since that time, Archuleta County has discontinued broadcast
herbicide use and mowing on ROWs within the species' range. However,
the planted exotic grasses continue to limit the species' habitat.
Highway ROWs provide about 9 percent of the occupied habitat for
Ipomopsis polyantha. All highway ROW habitat is at risk of disturbance
by construction of new access roads or acceleration lanes, bike paths,
and utilities installation or maintenance. Such construction results in
direct loss of I. polyantha individuals or reduced suitability of its
habitat by altering the soil characteristics (Anderson 2004, p. 36).
Summary of Factor A
We determined that the present and threatened destruction,
modification, and fragmentation of Ipomopsis polyantha habitat from
commercial, municipal, agricultural, and residential development,
associated new utility installations, construction of new access roads
and bike paths, competition from introduced roadside grasses, and other
impacts to highway ROWs are significant and imminent threats to the
species throughout its range. At this time, the species persists
primarily on private lands (about 86 percent) and highway ROWs (about 9
percent). Based on the rate of current and proposed development over
the entire range of the species, we estimate that 95 percent of the
species' habitat could be modified or destroyed within 5 to 10 years.
The plants would then be relegated to 10 ac (4 ha) of BLM land; 7.5 ac
(3 ha) of Town park land; small, fragmented portions of highway ROWs;
and a few, small, lightly used, private yards and pastures, thus
putting the species in danger of extinction.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Activities resulting in overutilization of Ipomopsis polyantha
plants for commercial, recreational, scientific, or educational
purposes are not known to exist. Therefore, we do not consider
overutilization for commercial, recreational, scientific, or
educational purposes to be a threat to the species now or in the
foreseeable future.
C. Disease or Predation
Disease
Disease is not known to affect Ipomopsis polyantha. Therefore, we
do not consider disease to be a threat to the species now or in the
foreseeable future.
Predation
This species is threatened by destruction of flowering plants,
rosettes, and seeds due to concentrated livestock disturbance and some
herbivory. Observations of the ``fence line effect''--healthy plants
outside the fence and impacted plants inside the fence--at several
locations on private land used for cattle and horse grazing indicate
that Ipomopsis polyantha does not tolerate intensive livestock grazing
(Anderson 2004, p. 30). For example, grazing by horses at a
residential/agricultural development within the Pagosa Springs
occurrence in 2005 resulted in few I. polyantha plants 3 years later
(Mayo 2008b, p. 2). Over-the-fence observations from seven locations
(pastures) in 2009 found few or no plants in the three heavily grazed
pastures and numerous plants in the adjacent pastures with light or no
grazing (Glenne and Mayo 2010, pp. 1-3). We do not know whether the
destruction of the plants was a result of herbivory or trampling. I.
polyantha is not found in heavily grazed pastures, but occurrences have
been observed in lightly grazed horse pastures and abandoned pastures
(CNAP 2007, p. 6). Plants could possibly recolonize a pasture if
livestock numbers were reduced sufficiently and the seed bank was still
viable, or if there was a seed source nearby, such as on the ungrazed
side of a fence. Indications are that the species may persist in areas
with light grazing, but the level of impact and the threshold of
species' tolerance have not been studied. Few plants persist in areas
of continual grazing (Collins 1995, pp. 107, 111, 112). We determined
that destruction of flowering plants, rosettes, and seeds due to heavy
livestock use is a significant and ongoing threat to I. polyantha now
and in the foreseeable future.
D. The Inadequacy of Existing Regulatory Mechanisms
Local Laws and Regulations
Town and county zoning ordinances have the potential to affect
Ipomopsis polyantha and its habitats. We know of no town or county
regulations that provide for protection or conservation of I. polyantha
or its habitat. As discussed under Factor A above, Archuleta County
road maintenance crews voluntarily
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refrain from mowing or broadcast spraying ROWs within the range of
Ipomopsis polyantha; however, there is no law, regulation, or policy
requiring them to do so. New annexation of 2,018 ac (817 ha) into the
Town of Pagosa Springs will change zoning from 35-ac (14-ha)
residential and agricultural parcels to commercial and small lot
residential, with anticipated adverse impacts to the Pagosa Springs
occurrence of I. polyantha, as described under Factor A above.
Decisions regarding annexations into the town and changes in allowable
subdividing of parcels in the county are currently being made to
encourage growth that will boost the local economy. Provisions for
avoidance or minimization of disturbance to habitat for the plants are
not included in these decisions or plans.
State Laws and Regulations
No State regulations protect rare plant species in Colorado.
Ipomopsis polyantha is classified by CNHP as a G1 and S1 species, which
means it is critically imperiled across its entire range and within the
State of Colorado (CNHP 2010b, pp. 1-5). The CDOT has drafted best
management practices for ROWs within I. polyantha habitat in
collaboration with the Service (Peterson 2008, p. 1), but the agreement
has not been finalized. In 2006, voluntary measures to minimize impacts
to plants from a sewer line installation along U.S. 84 were recommended
by CDOT and supervised by the county, but not implemented by the
contractors, as described under Factor A (Mayo 2008c, pp. 1-4; Peterson
2006, pp. 1-3).
Federal Laws and Regulations
Ipomopsis polyantha is on the sensitive species lists for the USFS
(2006, pp. 5, 6, 13, 15-20; USFS 2009, p. 6) and the BLM (2000, p. 3;
2008b, p. 47). Occupied habitat has not been found on USFS land, but
there is nearby habitat that appears to be suitable, so the species is
included in project clearance surveys on the forest. In 2006, we
estimated that the Dyke occurrence extended onto 20 ac (8 ha) of BLM
land (Lyon 2007b, pp. 3, 12, 13); 88 plants and 164 rosettes were found
there in 2007 (CNAP 2007, p. 2). In 2010, we revised the estimated
occupied BLM habitat to 9.9 ac (4.0 ha) (Service 2011a, p. 2). This BLM
parcel was withdrawn from a proposed land exchange so that the plant
habitat would remain under Federal management (Brinton 2009, pers.
comm.; Lyon 2007b, p. 3). We believe that BLM adequately protects
Ipomopsis polyantha on its lands pursuant to the Federal statutes and
regulations that guide Federal land management. However, so little of
the species' habitat occurs on BLM lands that the BLM can do little to
influence the overall status of the species.
Summary of Factor D
We reviewed the suite of existing regulatory mechanisms that could
potentially offer some protection to Ipomopsis polyantha, including the
Federal Land Policy and Management Act (FLPMA)(43 U.S.C. 1701 et seq.),
and State and local laws and determined that these existing regulatory
mechanisms are inadequate to address the primary threats to the
species. Ninety-seven percent of the known range of the species is on
State, Town, and private lands, affording the species little to no
protection on these lands. Federal statutes and regulations governing
natural resource protection apply only to 2.5 percent of the occupied
habitat and therefore can do little to influence the overall status of
the species. The State of Colorado offers no regulatory protection to
plants, which means that protection falls upon local County and Town
ordinances. The planning regulations governing growth in Archuleta
County and the Town of Pagosa Springs do not contain any requirements
to protect rare plants, including I. polyantha, when siting new growth
and development. In fact, the current county planning regulations
contribute to the risk of extinction for the species by facilitating
development in the last remaining habitat occupied by the species.
Therefore, we determined that existing regulatory mechanisms do not
adequately address the primary threats to the species.
E. Other Natural or Manmade Factors Affecting the Species' Continued
Existence
Habitat and Distribution
The adaptation of Ipomopsis polyantha to Pagosa-Winifred soils
derived from Mancos Shale limits it to about 6.5 square mi (16.8 square
km) within a 13-mi (21-km) range of fragmented habitat on outcrops of
Mancos Shale. The species has specific physiological requirements for
germination and growth that may prevent its spread to other locations
(Anderson 2004, pp. 23-24). In greenhouse trials, seeds will germinate
and grow on other soils, but they grow much faster on Mancos Shale
soils (Collins 1995, p. 114). Faster growth may give I. polyantha a
competitive advantage on relatively barren Mancos shale that it lacks
on other soils, where its smaller seedlings have more competition from
other plants for nutrients and water. The species produces more seed
when it is cross-pollinated (Anderson 2004, p. 23); therefore, existing
and foreseeable fragmentation of habitat may cause gene flow to be
obstructed. Pollinator-mediated pollen dispersal is typically limited
to the foraging distances of pollinators, and no bee species is
expected to travel more than 1 mi (1.6 km) to forage (Tepedino 2009, p.
11). Thus, it is likely that the Dyke occurrence, of about 270 plants
and 541 rosettes, is genetically isolated from the Pagosa Springs
occurrence 13 miles (21 kilometers) away. Spatially isolated plant
populations are at higher risk of extinction due to inbreeding
depression, loss of genetic heterogeneity, and reduced dispersal rates
(Silvertown and Charlesworth 2001, p. 185).
Transplanting
Rosettes in the path of power pole replacements were transplanted
to suitable habitat in the town park in 2007. The 278 transplants
survived the winter and produced about 27 flowering plants. However, no
surviving rosettes could be relocated in the fall of 2007, and no
evidence of trampling or habitat destruction was found (Coe 2007, pp.
2-3). Another attempt at transplanting rosettes, to save them from
destruction during utility installations in 2005, was not effective in
producing new rosettes in the third year (Brinton 2007, pers. comm.).
There was no evidence of trampling or habitat destruction with these
transplants. Unless effective methods are developed, most plants that
cannot be avoided during utility installations and construction
activities are unlikely to survive and reproduce. Whether the species
can survive translocation under other circumstances remains uncertain,
but at this time we consider transplantation an ineffective method of
mitigating the impacts of development. For this reason, we conclude
that the species is highly vulnerable to development because
populations cannot be successfully moved out of the way.
Fluctuating Population Size
Ipomopsis polyantha shows great differences in plant numbers from
year to year, probably because the plants are biennial and grow from
seed. This trait makes them more vulnerable than perennials to changes
in environment, including timing and amount of moisture and length of
time since disturbance. With increased time after disturbance,
competition from both native and nonnative plants increases (CNAP
2008a, p. 4). As a biennial species, I. polyantha also may be
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vulnerable to prolonged drought. During drought years, seeds may not
germinate and plants may remain as rosettes without flowering or
producing a new crop of seeds.
Climate Change
Habitat changes as a result of climate change could potentially
impact Ipomopsis polyantha. Localized projections indicate the
southwest United States may experience the greatest temperature
increase of any area in the lower 48 States (IPCC 2007, p. 30). A 10 to
30 percent decrease in precipitation in mid-latitude western North
America is projected by the year 2050, based on an ensemble of 12
climate models (Milly et al. 2005, p. 1). Climate modeling at this time
has not been refined to the level that we can predict the amount of
temperature and precipitation change within the limited range of I.
polyantha. Therefore, this analysis is speculative based on the data
available at this time. When plant populations are impacted by reduced
reproduction during drought years, they may require several years to
recover. Climate change may exacerbate the frequency and intensity of
droughts in this area and result in reduced species' viability as the
dry years become more common. As described above, I. polyantha is
sensitive to the timing and amount of moisture due to its biennial life
history. Thus, if climate change results in local drying, the species
could experience a reduction in its reproductive output.
Recent analyses of long-term data sets show accelerating rates of
climate change over the past 2 or 3 decades, indicating that the
extension of species' geographic range boundaries towards the poles or
to higher elevations by progressive establishment of new local
occurrences will become increasingly apparent in the short term (Hughes
2000, p. 60). The limited geographic range of the Mancos Shale
substrate that underlies the entire Ipomopsis polyantha habitat likely
limits the ability of the species to adapt by shifting occurrences in
response to climatic conditions.
Summary of Factor E
We determined that the natural and human-caused factors of specific
soil and germination requirements, fragmented habitat, effects of
drought and climate change, and lack of proven methods for propagation
and reintroduction present an imminent and moderate degree of threat to
Ipomopsis polyantha across the entire range of the species. These
factors make the species highly vulnerable to the development threats
described under Factor A, and it is highly unlikely that the species
could respond to these threats by extending its range.
Cumulative Impacts
Some of the threats discussed in this finding could work in concert
with one another to cumulatively create situations that potentially
impact Ipomopsis polyantha beyond the scope of each individual threat.
For example, as discussed under Factor A, destruction and modification
of habitat by clearing the ground, mowing and weed spraying, and
concentrated livestock grazing could reduce the number of available
pollinators for the plants by removing other species of blooming plants
that attract pollinators and by destroying the ground-nesting habitat
needed by bees. A reduction in bee pollinators could cause I. polyantha
to produce fewer seeds. Such cumulative impacts from development-
related activities are likely to impact the species, given the ubiquity
of development within the habitat.
We have not identified other likely scenarios where the threats
discussed in the five factors above have potential to interact
synergistically to produce threats to Ipomopsis polyantha beyond those
which we have analyzed.
Summary of Factors
The Pagosa Springs occurrence of Ipomopsis polyantha totals
approximately 342 ac (138 ha) of Ipomopsis polyantha habitat, including
3 mi (4.8 km) of highway ROW and the private properties on either side
of the highway. The smaller Dyke occurrence of about 46 ac (19 ha)
includes highway ROWs, private land, and 10 ac (4 ha) of BLM land.
Destruction of plants, when combined with the modification and
fragmentation of habitat within this small range, results in a
substantial loss to the viability of the species. Both known
occurrences face ongoing, new, and foreseeable threats, including
commercial, residential, agricultural, and municipal development;
associated road and utility improvements and maintenance; heavy
livestock use; inadequacy of existing regulatory mechanisms to address
the primary threats to the species; fragmented habitat; and prolonged
drought conditions. The magnitude of threat for I. polyantha is high
due to the direct overlap of ongoing and planned land development on 95
percent of the known habitat. The overall impact of current and planned
development is likely to result in extensive disturbance and
destruction of the remaining habitat within the foreseeable future of 5
to 10 years, depending on economic growth in the area, thus putting the
species in danger of extinction.
Species Information--Penstemon debilis
Description
Penstemon debilis is a rare plant, endemic to oil shale outcrops on
the Roan Plateau escarpment in Garfield County, Colorado. This species
is known by the common names Parachute beardtongue and Parachute
penstemon. P. debilis is classified by the CNHP as a G1 and S1 species,
which means it is critically imperiled across its entire range and
within the State of Colorado (CNHP 2010b, pp. 6-10). Traditionally, the
genus Penstemon was included in the Scrophulariaceae (figwort) family.
However, Penstemon is now considered to be within the Plantaginaceae
(plantain) family due to recent research using DNA seq