Endangered and Threatened Wildlife and Plants; Endangered Species Status for Franklin's Bumble Bee, 47221-47238 [2021-17832]
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[FR Doc. 2021–17713 Filed 8–23–21; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R1–ES–2018–0044;
FF09E21000 FXES11110900000 212]
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RIN 1018–BD25
Endangered and Threatened Wildlife
and Plants; Endangered Species
Status for Franklin’s Bumble Bee
AGENCY:
Fish and Wildlife Service,
Interior.
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8/24/2021, [Insert Federal Register citation].
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ACTION:
PART 70—STATE OPERATING PERMIT
PROGRAMS
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3/30/2021
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Final rule.
We, the U.S. Fish and
Wildlife Service (Service), are listing the
Franklin’s bumble bee (Bombus
franklini), an invertebrate species from
Douglas, Jackson, and Josephine
Counties in Oregon, and Siskiyou and
Trinity Counties in California, as an
endangered species under the
Endangered Species Act of 1973, as
amended (Act). This rule adds this
species to the Federal List of
Endangered and Threatened Wildlife
and applies the protections of the Act to
this species. We are not designating
critical habitat for the Franklin’s bumble
bee because we determined that such a
designation would not be beneficial to
the species.
DATES: This rule is effective September
23, 2021.
ADDRESSES: This final rule and
supporting documents are available on
the internet at https://
www.regulations.gov in Docket No.
FWS–R1–ES–2018–0044, or at https://
ecos.fws.gov.
FOR FURTHER INFORMATION CONTACT: Paul
Henson, Field Supervisor, U.S. Fish and
Wildlife Service, Oregon Fish and
Wildlife Office, 2600 SE 98th Ave.,
Suite 100, Portland, OR 97266;
telephone 503–231–6179. Persons who
use a telecommunications device for the
deaf (TDD) may call the Federal Relay
Service at 800–877–8339.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Executive Summary
Why we need to publish a rule. Under
the Act, if we determine that a species
may be an endangered or threatened
species throughout all or a significant
portion of its range, we are required to
promptly publish a proposal in the
Federal Register and make a
determination on our proposal within 1
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year. To the maximum extent prudent
and determinable, we must designate
critical habitat for any species that we
determine to be an endangered or
threatened species under the Act.
Listing a species as an endangered or
threatened species and designation of
critical habitat can only be completed
by issuing a rule.
What this document does. This rule
lists Franklin’s bumble bee (Bombus
franklini) as an endangered species
under the Act. We are not designating
critical habitat because we determined
that a designation is not prudent for this
species.
The basis for our action. Under the
Act, we may determine that a species is
an endangered or threatened species
because of any of five factors: (A) The
present or threatened destruction,
modification, or curtailment of its
habitat or range; (B) overutilization for
commercial, recreational, scientific, or
educational purposes; (C) disease or
predation; (D) the inadequacy of
existing regulatory mechanisms; or (E)
other natural or manmade factors
affecting its continued existence. We
have determined that Franklin’s bumble
bee meets the definition of an
endangered species and therefore
warrants protection under the Act. The
threats to the species of pathogens,
pesticides, and small population size
are ongoing and rangewide; they are
likely to continue to act individually
and in combination to decrease the
viability of the Franklin’s bumble bee.
The risk of extinction is high, the
suspected threats to the species persist,
and the number of remaining Franklin’s
bumble bees is presumably very small,
as the species has not been observed
since 2006. Existing regulatory
mechanisms or conservation measures
in place do not appreciably reduce or
ameliorate the existing threats to the
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species, as evidenced by the species’
acute and rangewide decline. Therefore,
on the basis of the best available
scientific and commercial information,
we are listing the Franklin’s bumble bee
as endangered in accordance with
sections 3(6) and 4(a)(1) of the Act.
Section 4(a)(3) of the Act requires the
Secretary of the Interior (Secretary) to
designate critical habitat concurrent
with listing to the maximum extent
prudent and determinable. Section
3(5)(A) of the Act defines critical habitat
as (i) the specific areas within the
geographical area occupied by the
species, at the time it is listed, on which
are found those physical or biological
features (I) essential to the conservation
of the species and (II) which may
require special management
considerations or protections; and (ii)
specific areas outside the geographical
area occupied by the species at the time
it is listed, upon a determination by the
Secretary that such areas are essential
for the conservation of the species.
Section 4(b)(2) of the Act states that the
Secretary must make the designation on
the basis of the best scientific data
available and after taking into
consideration the economic impact, the
impact on national security, and any
other relevant impacts of specifying any
particular area as critical habitat.
Because the present or threatened
destruction, modification, or
curtailment of habitat is not a threat to
the Franklin’s bumble bee (disease and
other manmade factors are likely the
primary threat to the species within its
habitat), in accordance with 50 CFR
424.12(a)(1), we determine that
designating critical habitat is not
prudent for Franklin’s bumble bee.
Peer review and public comment. We
sought the expert opinions of 10
appropriate and independent specialists
regarding the species status assessment
report. We received responses from 5
specialists, which informed our
determination. We also considered all
53 comments and information received
from the public during the comment
period.
Previous Federal Actions
Please refer to the proposed rule (84
FR 40006) for Franklin’s bumble bee
published on August 13, 2019, for a
detailed description of previous Federal
actions concerning this species.
On August 27, 2019, the Service
published a final rule (84 FR 45020)
revising the regulations at 50 CFR part
424 for listing species and designating
critical habitat. However, the revisions
apply only to relevant rulemakings for
which the proposed rule is published
after September 26, 2019, the effective
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date of the final rule. Thus, the prior
version of the regulations at 50 CFR part
424 continues to apply to any
rulemakings for which a proposed rule
was published before September 26,
2019, including this final rule for
Franklin’s bumble bee.
Summary of Changes From the
Proposed Rule
We considered all comments and
information we received during the
comment period for the proposed rule to
list the Franklin’s bumble bee (84 FR
40006; August 13, 2019). Based on these
comments and additional internal
review, we made the following changes
from the proposed rule in this final rule:
• Added to this rule and the SSA
report additional climate change
information and analysis, as well as
discussion on the likely effects of other
potential threats in the future;
• Updated this rule and the SSA
report with information from the 2019
survey season;
• Corrected a mathematical error in
our presentation of neonicotinoid
pesticide applications in the historical
range of the species in this rule and in
the SSA report;
• Added information from the SSA
report to this rule regarding nectaring
behavior, as well as the
commercialization of bumble bees for
pollination;
• Updated information in this rule on
pesticide regulation on National
Wildlife Refuge System lands;
• Added further detail in the rule on
Tribal notifications;
• Added several citations and
clarifications to the rule to further
support content; and
• Made minor editorial changes to the
rule to improve readability.
We carefully considered the
additional information we received
during the comment period, and while
much of this information was helpful, it
did not result in any further changes
from our proposal to this final rule to
list Franklin’s bumble bee as
endangered, nor did it result in a change
to our determination that designation of
critical habitat is not prudent at this
time.
Supporting Documents
A species status assessment (SSA)
team prepared an SSA report for
Franklin’s bumble bee. The SSA team
was composed of Service biologists, in
consultation with other species experts.
The SSA report represents a
compilation of the best scientific and
commercial data available concerning
the status of the species, including the
impacts of past, present, and future
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factors (both negative and beneficial)
affecting the species.
In accordance with our joint policy on
peer review published in the Federal
Register on July 1, 1994 (59 FR 34270),
we sought the expert opinions of 10
appropriate and independent specialists
regarding the scientific basis for this
proposed rule, detailed in the Franklin’s
Bumble Bee Species Status Assessment
report (SSA report) (Service 2018a,
entire). We received five reviews. The
purpose of peer review is to ensure that
our listing and critical habitat
determinations are based on
scientifically sound data, assumptions,
and analyses. The peer reviewers have
expertise in Franklin’s bumble bee or
Bombus biology and habitat, and their
comments helped inform our
determinations. We also invited
comment on the SSA report from our
partner agencies; the U.S. Forest
Service, the Bureau of Land
Management, and the Oregon
Department of Agriculture provided us
with comments. The comments from
peer and partner reviews were carefully
considered in the process of finalizing
the SSA report that provided the
scientific basis for both the proposed
rule and this final rule. These
comments, along with other public
comments on our proposed rule, are
available in the docket for this final rule
(https://www.regulations.gov in Docket
No. FWS–R1–ES–2018–0044).
I. Final Listing Determination
Background
A thorough review of the taxonomy,
life history, and ecology of Franklin’s
bumble bee is presented in the SSA
report (Service 2018a, entire) on https://
www.regulations.gov under Docket No.
FWS–R1–ES–2018–0044. Franklin’s
bumble bee is thought to have the most
limited distribution of all known North
American bumble bee species
(Plowright and Stephen 1980, p. 479;
Xerces Society and Thorp 2010, p. 6),
and one of the most limited geographic
distributions of any bumble bee in the
world (Frison 1922, p. 315; Williams
1998, p. 129). The species has been
recorded from the Umpqua and Rogue
River Valleys in Oregon (Stephen 1957,
p. 81) and from northern California,
suggesting its restriction to the Klamath
Mountain region of southern Oregon
and northern California (Thorp et al.
1983, p. 8). Elevations where it has been
observed range from 162 meters (m)
(540 feet (ft)) in the northern part of its
range, to over 2,340 m (7,800 ft) in the
southern part of its range. All confirmed
specimens have been found in an area
about 306 kilometers (km) (190 miles
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(mi)) to the north and south, and 113 km
(70 mi) east to west, between 122° to
124° west longitude and 40° 58′ to 43°
30′ north latitude in Douglas, Jackson,
and Josephine Counties in southern
Oregon, and Siskiyou and Trinity
Counties in northern California (Thorp
1999, p. 3; Thorp 2005, p. 1;
International Union for Conservation of
Nature 2009, p. 1).
Franklin’s bumble bee was first
observed in 1917, and first described in
1921, and limited occurrence and
observation data exist for Franklin’s
bumble bee prior to 1998. The species
has been found on many privately
owned sites as well as municipal, State,
and Federal land. Historical
observations and occurrence data for
Franklin’s bumble bee prior to 1998
include opportunistic observations,
student collections, and museum
specimens, as well as the collections
and notes of interested parties, natural
resource managers, and university staff
(Xerces Society and Thorp 2010, pp. 34–
40). A more intensive and targeted
search effort for the species began in
1998, in areas thought to have the
highest likelihood of Franklin’s bumble
bee presence. There was initial success
at finding a higher abundance of the
species than ever previously reported;
in one year (1998), 98 Franklin’s bumble
bees were observed (mostly from two
sites). However, in subsequent years,
searchers found fewer and fewer
Franklin’s bumble bees, and none have
been found since the last sighting of a
single individual in Oregon in 2006.
The variations in timing, scope,
intensity, and methodology of search
efforts (including those since 1998) and
the lack of observations since 2006
prevent the identification of any
population trends. Many of the
occurrence records provide only point
data for an occurrence, with no details
on the size of the area searched or
whether or not the record reflected a
comprehensive search of an area. Many
records also lack details on the level of
survey effort per location (number of
searchers, hours of search effort per day,
number of days per search effort).
The lack of systematic surveys across
the historical range of the species over
time prevents us from using occurrence
records to extrapolate reasonable
estimates of species abundance or
distribution or from concluding that the
species is extinct. Even though none
have been seen since 2006, Franklin’s
bumble bee populations could
potentially persist undetected. The areas
chosen for survey were selected due to
a combination of abundance of floral
resources throughout the colony cycle,
relatively recent historical occurrence of
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the species, and accessibility to
surveyors. However, the surveyed area
represents a relatively small percentage
of the historical range of the Franklin’s
bumble bee; therefore, it is possible the
species may persist in other areas of the
range. There are numerous instances of
species rediscovered after many years,
even decades, of having been believed
extinct (e.g., Scheffers et al. 2011,
entire). As one example of such a case,
the Fender’s blue butterfly (Icaricia
icarioides fenderi) of Oregon was
believed extinct after the last recorded
observation in 1937, until it was
rediscovered in 1989, 52 years later
(Hammond and Wilson 1992, p. 175;
Hammond and Wilson 1993, p. 2).
Recent approaches to evaluating
extinction likelihood place increased
emphasis on the extensiveness and
adequacy of survey effort (Keith et al.
2017, p. 321; Thompson et al. 2017, p.
328), and caution against declaring a
species as extinct in the face of
uncertainty (Akc¸akaya et al. 2017, p.
340).
The specific life-history
characteristics and behavior of this rare
species have not been studied; much of
the information presented in the SSA
report (Service 2018a, entire) is inferred
from information on Bombus in general
and some closely related species
(western bumble bee (B. occidentalis),
rusty patched bumble bee (B. affinis),
and yellow-faced bumble bee (B.
vosnesenskii), among others). The report
also relied heavily on information from
species experts (Service 2018a, entire).
Franklin’s bumble bee is a primitively
eusocial bumble bee, meaning they are
highly social and adults have flexible
roles in their social order. They live in
colonies made up of a queen and her
male and worker offspring, and adult
females can switch from worker to
queen roles. Like other eusocial Bombus
species, Franklin’s bumble bee typically
nests underground in abandoned rodent
burrows or other cavities that offer
resting and sheltering places, food
storage, nesting, and room for the
colony to grow (Plath 1927, pp. 122–
128; Hobbs 1968, p. 157; Thorp et al.
1983, p. 1; Thorp 1999, p. 5). The
species may also occasionally nest on
the ground (Thorp et al. 1983, p. 1) or
in rock piles (Plowright and Stephen
1980, p. 475). It has even been found
nesting in a residential garage in the city
limits of Medford, Oregon (Thorp 2017,
pers. comm.).
Colonies of Franklin’s bumble bee
have an annual cycle, initiated each
spring when solitary queens emerge
from hibernation and seek suitable nest
sites (Thorp 2017, pers. comm.).
Colonies may contain from 50 to 400
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workers along with the founding queen
(Plath 1927, pp. 123–124; Thorp et al.
1983, p. 2; Macfarlane et al. 1994, p. 7).
Two colonies of Franklin’s bumble bee
that were initiated in the laboratory and
set out to complete development in the
field contained over 60 workers by early
September, and likely produced over
100 workers by the end of the season
(Plowright and Stephen 1980, p. 477).
The flight season of Franklin’s bumble
bee is from mid-May to the end of
September (Thorp et al. 1983, p. 30); a
few individuals have been encountered
in October (Southern Oregon University
Bee Collection records, in Xerces
Society and Thorp 2010, Appendix 1, p.
39). At the end of the colony cycle, all
the workers and the males die along
with the founding queen; only the
inseminated hibernating females (gynes)
are left to carry on the genetic lineage
into the following year (Duchateau and
Velthius 1988).
As with all Bombus species,
Franklin’s bumble bee has a unique
genetic system called the haplodiploid
sex determination system. In this
system, unfertilized (haploid) eggs
become males that carry a single set of
chromosomes, and fertilized (diploid)
eggs become females that carry two sets
of chromosomes. This system may result
in lower levels of genetic diversity than
the more common diploid-diploid sex
determination system, in which both
males and females carry two sets of
chromosomes. Haplodiploid organisms
may be more prone to population
extinction than diploid-diploid
organisms, due to their susceptibility to
low population levels and loss of
genetic diversity (Service 2018a, p. 37).
Inbreeding depression in bumble bees
can lead to the production of sterile
diploid males (Goulson et al. 2008, p.
11.7) and negatively affects bumble bee
colony size (Herrman et al. 2007, p.
1167), which are key factors in a
colony’s reproductive success.
As one of the rarest Bombus species,
Franklin’s bumble bees are somewhat
enigmatic, and a specific habitat study
for the species has not been completed.
Such a study was initiated in 2006,
when the Franklin’s bumble bee was
last seen, but could not continue due to
the subsequent absence of the species
(Thorp 2017, pers. comm.). However,
some general habitat associations of
Bombus are known. Like all bumble
bees, the Franklin’s bumble bee requires
a constant and diverse supply of flowers
that bloom throughout the colony’s life
cycle, from spring to autumn (Xerces
Society and Thorp 2010, p. 11); these
resources would typically be found in
open (non-forested) meadows in
proximity to seeps and other wet
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meadow environments. The nectar from
flowers provides carbohydrates, and the
pollen provides protein. Franklin’s
bumble bee may have a foraging
distance of up to 10 km (6.2 mi) (Thorp
2017, pers. comm.), but the species’
typical dispersal distance is most likely
3 km (1.86 mi) or less (Hatfield 2017,
pers. comm.; Goulson 2010, p. 96).
Franklin’s bumble bee have been
observed collecting pollen from lupine
(Lupinus spp.) and California poppy
(Eschscholzia californica), and
collecting nectar from horsemint or
nettle-leaf giant hyssop (Agastache
urticifolia) and mountain monardella
(Monardella odoratissima) (Xerces
Society and Thorp 2010, p. 11).
Franklin’s bumble bee may also collect
both pollen and nectar from vetch (Vicia
spp.), as well as rob nectar from it
(Xerces Society and Thorp 2010, p. 11).
Short-tongued species, including
Franklin’s bumble bee, sometimes visit
flowers that are quite elongated and
have difficulty reaching nectar deep in
the flower. These bees can ‘rob nectar’
by chewing a hole on the outside of the
flower at the base, through which they
can easily reach the nectar with their
tongues.
In summary, Franklin’s bumble bee
has been found in a wide array of
sheltered and exposed habitat types at a
broad elevational range, and the species
appears to be a generalist forager.
Despite uncertainties regarding the
species’ habitat needs, we know they
need (1) floral resources for nectaring
throughout the colony cycle, and (2)
relatively protected areas for breeding
and shelter. The habitat elements that
Franklin’s bumble bee appears to prefer
to fulfill those needs mentioned above
are relatively plentiful and widely
distributed.
Regulatory and Analytical Framework
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Regulatory Framework
Section 4 of the Act (16 U.S.C. 1533)
and its implementing regulations (50
CFR part 424) set forth the procedures
for determining whether a species is an
‘‘endangered species’’ or a ‘‘threatened
species.’’ The Act defines an
endangered species as a species that is
‘‘in danger of extinction throughout all
or a significant portion of its range,’’ and
a threatened species as a species that is
‘‘likely to become an endangered
species within the foreseeable future
throughout all or a significant portion of
its range.’’ The Act requires that we
determine whether any species is an
‘‘endangered species’’ or a ‘‘threatened
species’’ because of any of the following
factors:
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(A) The present or threatened
destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial,
recreational, scientific, or educational
purposes;
(C) Disease or predation;
(D) The inadequacy of existing
regulatory mechanisms; or
(E) Other natural or manmade factors
affecting its continued existence.
These factors represent broad
categories of natural or human-caused
actions or conditions that could have an
effect on a species’ continued existence.
In evaluating these actions and
conditions, we look for those that may
have a negative effect on individuals of
the species, as well as other actions or
conditions that may ameliorate any
negative effects or may have positive
effects.
We use the term ‘‘threat’’ to refer in
general to actions or conditions that are
known to or are reasonably likely to
negatively affect individuals of a
species. The term ‘‘threat’’ includes
actions or conditions that have a direct
impact on individuals (direct impacts),
as well as those that affect individuals
through alteration of their habitat or
required resources (stressors). The term
‘‘threat’’ may encompass—either
together or separately—the source of the
action or condition or the action or
condition itself.
However, the mere identification of
any threat(s) does not necessarily mean
that the species meets the statutory
definition of an ‘‘endangered species’’ or
a ‘‘threatened species.’’ In determining
whether a species meets either
definition, we must evaluate all
identified threats by considering the
expected response by the species, and
the effects of the threats—in light of
those actions and conditions that will
ameliorate the threats—on an
individual, population, and species
level. We evaluate each threat and its
expected effects on the species, then
analyze the cumulative effect of all of
the threats on the species as a whole.
We also consider the cumulative effect
of the threats in light of those actions
and conditions that will have positive
effects on the species, such as any
existing regulatory mechanisms or
conservation efforts. The Secretary
determines whether the species meets
the definition of an ‘‘endangered
species’’ or a ‘‘threatened species’’ only
after conducting this cumulative
analysis and describing the expected
effect on the species now and in the
foreseeable future.
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Analytical Framework
The SSA report documents the results
of our comprehensive biological review
of the best available scientific and
commercial data regarding the status of
the species, including an assessment of
the potential threats to the species. The
SSA report does not represent a
decision by the Service on whether the
species should be listed as an
endangered or threatened species under
the Act. It does, however, provide the
scientific basis that informs our
regulatory decisions, which involve the
further application of standards within
the Act and its implementing
regulations and policies. The following
is a summary of the key results and
conclusions from the SSA report; the
full SSA report can be found at Docket
No. FWS–R1–ES–2018–0044 on https://
www.regulations.gov.
To assess the viability of Franklin’s
bumble bee, we used the three
conservation biology principles of
resiliency, redundancy, and
representation (Shaffer and Stein 2000,
pp. 306–310). Briefly, resiliency
supports the ability of the species to
withstand environmental and
demographic stochasticity (for example,
wet or dry, warm or cold years),
redundancy supports the ability of the
species to withstand catastrophic events
(for example, droughts, large pollution
events), and representation supports the
ability of the species to adapt over time
to long-term changes in the environment
(for example, climate changes). In
general, the more resilient and
redundant a species is and the more
representation it has, the more likely it
is to sustain populations over time, even
under changing environmental
conditions. Using these principles, we
identified the species’ ecological
requirements for survival and
reproduction at the individual,
population, and species levels, and
described the beneficial and risk factors
influencing the species’ viability.
The SSA process can be categorized
into three sequential stages. During the
first stage, we evaluated the individual
species’ life-history needs. The next
stage involved an assessment of the
historical and current condition of the
species’ demographics and habitat
characteristics, including an
explanation of how the species arrived
at its current condition. The final stage
of the SSA involved making predictions
about the species’ responses to positive
and negative environmental and
anthropogenic influences. Throughout
all of these stages, we used the best
available information to characterize
viability as the ability of a species to
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sustain populations in the wild over
time. We use this information to inform
our regulatory decision.
Summary of Biological Status and
Threats
In this discussion, we review the
biological condition of the species and
its resources, and the threats that
influence the species’ current and future
condition, in order to assess the species’
overall viability and the risks to that
viability.
To assess resiliency and redundancy,
we evaluated the change in Franklin’s
bumble bee occurrences (populations)
over time. To assess representation (as
an indicator of adaptive capacity) of the
Franklin’s bumble bee, we evaluated the
spatial extent of occurrences over time.
We evaluated the change in resiliency,
representation, and redundancy from
the past until the present; however, due
to the lack of observations of the species
since 2006, we did not project
anticipated future states of these
conditions.
Our analyses indicate that the
resiliency, redundancy, and
representation of the Franklin’s bumble
bee have all declined since the late
1990s. Historically, the species has
always been rare and has one of the
narrowest distributions of any Bombus
species in the world. Even so, the
abundance and distribution of
Franklin’s bumble bee has declined
significantly (Service 2018a, pp. 10–14);
the species has not been observed since
2006, despite intensive survey efforts in
select portions of its historical range.
Search efforts for the species have been
varied in timing, scope, intensity, and
methodology. During the more intensive
surveys from 1998 until the last
observation in 2006, the Franklin’s
bumble bee was observed at 14
locations, including 8 locations where it
had not been previously documented. In
1998, 98 bees were found among 11
locations. Searchers found fewer and
fewer bees after that year even though
they continued extensive searches in
multiple locations with the highest
likelihood of finding the species.
Twenty bees were located in 1999, nine
individuals were observed in 2000, and
one individual was observed in 2001.
Although 20 Franklin’s bumble bees
were observed in 2002, only 3 were
observed in 2003 (all at a single
locality), and a single worker bee was
observed in 2006. Despite continued
intensive search efforts in these areas
through 2019, there have been no
confirmed observations of the Franklin’s
bumble bee since 2006. Data allow us to
estimate 43 potential populations of the
species since 1921, when the first
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description of the species was published
(Service 2018a, pp. 11). From 1998 to
2006, we identified 14 potential
populations. Since 2006, no populations
have been located.
The vulnerability resulting from the
Franklin’s bumble bee’s haplodiploid
genetic system, as well as the loss in the
abundance and spatial extent of its
populations, suggest the resiliency,
representation, and redundancy of the
Franklin’s bumble bee have all declined
significantly since the late 1990s. The
losses in both the number of
populations and their spatial extent
render the Franklin’s bumble bee
vulnerable to extinction even without
further external stressors (e.g.,
pathogens and insecticide exposure)
acting upon the species.
As part of our status assessment of the
Franklin’s bumble bee, we looked at
potential stressors affecting the species’
viability (Service 2018a, pp. 23–40).
Potential stressors that we analyzed for
the Franklin’s bumble bee generally fit
into three groups that correspond with
Factors A (habitat loss and
fragmentation), C (pathogens), or E
(pesticide use, competition with
nonnative bees, and effects of small
population size). No potential stressors
of the Franklin’s bumble bee correspond
with Factor B. There has never been any
indication that the Franklin’s bumble
bee was at risk of overutilization for
commercial, recreational, scientific, or
educational purposes, and we did not
find any new information to suggest this
has changed. Existing regulatory
mechanisms (Factor D) are discussed
below in the context of how they help
to reduce or ameliorate stressors to the
Franklin’s bumble bee.
The 2010 petition identified
destruction, degradation, and
conversion of habitat as a threat to the
Franklin’s bumble bee. In our 90-day
finding on the 2010 petition (76 FR
56381; September 13, 2011), we noted
that the petitioners provided substantial
information on threats to the Franklin’s
bumble bee from the destruction,
modification, or curtailment of habitat,
primarily due to the potential impacts of
natural or prescribed fire. Because the
loss and degradation of habitat has been
shown to reduce both diversity and
abundance in other Bombus species
(Potts et al. 2010, pp. 348–349), we
looked at the potential stressors of
natural or prescribed fire, agricultural
intensification, urban development,
livestock grazing, and the effects of
climate change (Service 2018a, pp. 23–
40).
Although conversion of natural
habitat appears to be the primary cause
of bumble bee habitat loss throughout
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the world (Goulson et al. 2015, p. 2;
Kosior et al. 2010, p. 81), many
researchers believe it is unlikely to be a
main driver of the recent, widespread
North American bee declines (Szabo et
al. 2012, p. 236; Colla and Packer 2008,
p. 1388; Cameron et al. 2011, p. 665).
Despite uncertainties regarding the
Franklin’s bumble bee’s habitat needs,
we know they need (1) floral resources
for nectaring throughout the colony
cycle, and (2) relatively protected areas
for breeding and shelter. Furthermore,
the available information regarding
locations where the species has been
found indicates that the Franklin’s
bumble bee is a generalist forager and
that the species’ specific needs and
preferences for these habitat elements
are relatively flexible, plentiful, and
widely distributed. While we can say
that Bombus species in general might
prefer protected meadows with an
abundance of wildflowers, the
Franklin’s bumble bee has been found
in a wide array of sheltered and exposed
habitat types at elevations ranging from
540 ft (162 m) to 7,800 ft (2,340 m)
(Thorp 2017, pers. comm.).
Natural or Prescribed Fire
Fire caused by both natural and
human-caused factors has been an
important change on the landscape in
the range of the Franklin’s bumble bee.
Because fire reduces natural succession
of forests through the burning of
encroaching woody plants, fire is a
primary factor in the maintenance of
grassland and meadow habitat that can
support Bombus species (Shultz and
Crone 1998, p. 244; Huntzinger 2003, p.
2). With the increase in human
development came fire suppression to
limit damage to manmade structures.
Fire suppression allows woody
encroachment to occur, and the diverse
landscape created by fire (open areas
mixed within forested areas) is slowly
being replaced by increasing areas of
denser forested habitat; the open areas
that facilitated the growth of diverse
understory plant communities are being
reduced from their historical condition
(Ruchty 2011, p. 26). Conifer species
now cover some of the area that was
previously open meadow habitat in the
range of the Franklin’s bumble bee
(Panzer 2002, p. 1297; Shultz and Crone
1998, p. 244). Although this loss of
habitat by fire suppression may have
limited the availability and diversity of
floral resources, as well as nest and
overwintering habitat for the Franklin’s
bumble bee, healthy meadow habitat
remains in areas where the Franklin’s
bumble bee was previously found
(Godwin 2017, pers comm.; Colyer
2017, pers. comm.), and it is unlikely
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that loss of habitat from fire suppression
was a factor in the decline of the
species.
Increased fuel loads from fire
suppression heighten the potential for
catastrophic, large-scale, and high
temperature wildfires. Any Bombus
colonies in the path of this type of fire
would be at risk of extirpation. Wildfire
may have extirpated some historical
populations of the Franklin’s bumble
bee, but we have no information
suggesting that any known Franklin’s
bumble bee occurrence sites were in the
path of catastrophic wildfires at the time
the sites were occupied. Controlled
burning became a management tool for
reducing potential fuel loads for
wildfire; controlled burning is carried
out by Federal land management
agencies including the U.S. Forest
Service and Bureau of Land
Management in the range of the
Franklin’s bumble bee. The effects of
fire on invertebrates depends greatly on
the biology of the specific taxa (Gibson
et al. 1992, p. 166), and in the case of
the Franklin’s bumble bee, controlled
burns could certainly cause death of
individual bees and negative effects to
a colony. Prescribed fire is likely to
continue to be used as a management
tool on some Federal land; however, the
practice is overall small in scale,
opportunistic (depending on weather,
funding, and a host of other factors),
used to prevent catastrophic fire, and
often a net benefit to pollinators as it
opens habitat by decreasing canopy
cover (U.S. Forest Service 1989, IV 87 to
IV 90, IV–113 to IV–119; U.S. Forest
Service 1990, pp 4–149 to 4–179). In
summary, we have no information to
indicate that controlled burns were a
factor in the decline of the Franklin’s
bumble bee or will increase in the future
to a degree that may affect the viability
of the species.
Agricultural Intensification
Agricultural intensification can result
in habitat loss for bumble bees, as these
practices often result in the planting of
monocultures that tend to provide floral
resources for a limited period of time,
rather than throughout the colony’s life
cycle. Agricultural intensification can
negatively impact wild bees by reducing
floral resource diversity and abundance
(Service 2018a, p. 32). Agricultural
intensification was determined to be a
primary factor leading to the local
extirpation and decline of bumble bees
in Illinois (Grixti et al. 2009, p. 75). An
increased use of herbicides often
accompanies development and
agricultural intensification, and the
widespread use of herbicides in
agricultural, urban, and even natural
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landscapes has led to decreases in
flowering plants (Potts et al. 2010, p.
350).
Within the historical range of the
Franklin’s bumble bee, total acres in
agricultural cropland decreased in all
three counties in Oregon (Douglas,
Jackson, and Josephine) by greater than
50 percent from 1997 to 2012 (U.S.
Department of Agriculture—National
Agriculture Statistics Service 2017, pers.
comm.; Service 2018a, p. 33). While the
total number of acres of agricultural
cropland is not synonymous with
agricultural intensification (specifically,
the expansion of monocultures), a
decrease in total acres of agriculture
leads us to conclude that agricultural
intensification was not likely a factor in
the decline of the Franklin’s bumble
bee. We have no documentation in our
files or any direct evidence that
agricultural intensification has
contributed to the decline of the
Franklin’s bumble bee or will increase
in the future to a degree that may affect
the viability of the species.
Approximately 42 percent of sites where
Franklin’s bumble bees have ever been
reported (18 of 43) occur on federally
owned land, primarily U.S. Forest
Service and Bureau of Land
Management land; very little habitat on
these lands has been permanently
altered or lost through agricultural
intensification (Service 2018a, p. 32).
Urban Development
Ongoing urbanization contributes to
the loss and fragmentation of natural
habitats. Urban gardens and parks
provide habitat for some pollinators,
including bumble bees (Frankie et al.
2005, p. 235; McFrederick and LeBuhn
2006, p. 372), but they tend not to
support the species richness of bumble
bees that can be found in nearby
undeveloped landscapes (Xerces Society
and Thorp 2010, p. 13) or that which
was present historically (McFrederick
and LeBuhn 2006). However, Franklin’s
bumble bee and western bumble bee
have both been observed in urban areas
of Ashland, Oregon, and in residential
areas of Medford, Oregon. Furthermore,
approximately 42 percent of the sites
where Franklin’s bumble bee have ever
been reported (18 of 43) occur on
federally owned land, primarily U.S.
Forest Service and Bureau of Land
Management land, and very little habitat
on these lands has been permanently
altered or lost through development.
Generally good habitat conditions
currently exist throughout the known
historical Franklin’s bumble bee
locations and all of the recent focused
survey areas. Two notable events
occurred in areas with previous
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observations of Franklin’s bumble bee:
The creation of Lake Applegate upon
the completion of Applegate Dam in the
fall of 1980, and a report of soil
modification on a portion of the Gold
Hill site in 2004; however, we have no
information to indicate that Franklin’s
bumble bees were still in the vicinity or
had any colonies in the area when these
events occurred. The Applegate Dam
project inundated two sites with
historical observations of Franklin’s
bumble bee (from the 1960s), but no
subsequent search efforts or
observations (Xerces Society and Thorp
2010, p. 13; Thorp, pers. comm. 2017).
The June 23, 2010, petition noted that
in 2004, soil had been excavated and
deposited in a portion of the Gold Hill
area (Xerces Society and Thorp 2010, p.
13). The last observation of Franklin’s
bumble bee at Gold Hill was in the year
2000, and the site was revisited 14 times
over the next 3 years with no
observations of Franklin’s bumble bee.
In both of these cases, we have no
information to suggest the species was
still using the habitat in the area by the
time the activities took place, and
therefore no information to suggest that
either of these events affected the
resiliency of any population of
Franklin’s bumble bee. We have no
documentation in our files or any direct
evidence that urbanization or
development in the range of Franklin’s
bumble bee, or the incidents described
above, contributed to the decline of the
species or will increase in the future to
a degree that may affect the viability of
the species (Portland State University
2015, p. 7).
Livestock Grazing
Livestock grazing occurs on public
land in much of the historical range of
the Franklin’s bumble bee. Overgrazing
by sheep between 1890 and 1920
resulted in trampling vegetation and
denuding soils, and grazing is currently
evident today in the continuing erosion
of the granitic soils of the McDonald
Basin, Siskiyou Gap, Mt. Ashland, and
the Siskiyou Crest (LaLande 1995, p. 31;
T. Atzet 2017, pers. comm.). Several
studies on the impacts of livestock
grazing on bees suggest that an increase
in the intensity of livestock grazing
affects the species richness of bees
(Service 2018a, p. 35). In contrast,
grazing, especially by cattle, can play a
key positive role in maintaining the
abundance and species richness of
preferred bumble bee forage (Carvell
2002, p. 44). Evidence of livestock
grazing was observed interspersed
within abundant floral resources in
Franklin’s bumble bee habitat during
several recent targeted survey efforts
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(Brooks 1997, pers. comm.; Service
2016, entire; Service 2017, entire; Trail
2017, pers. comm.). We have no new
information that the timing, location,
intensity, or duration of grazing has
changed, with the exception of the
Cascade-Siskiyou National Monument,
where most grazing has been retired
(Colyer 2018, pers. comm.). The lack of
specific information on the impacts of
livestock grazing on the Franklin’s
bumble bee limits our ability to connect
the activity to any specific species’
response, and we do not anticipate
grazing will increase in the future to a
degree that may affect the viability of
the species (Bureau of Land
Management 2016, pp. 96–103).
Effects of Climate Change
Specific impacts of climate change on
pollinators are not well understood;
most of the existing information on
climate change impacts to pollinators
comes from studies on butterflies.
Studies specifically relating to bumble
bees are scant, and we found no climate
change information specific to the
Franklin’s bumble bee. Changes in
temperature and precipitation, and the
increased frequency of storm events, can
affect pollinator population sizes
directly, by affecting survival and
reproduction (Intergovernmental Panel
on Climate Change 2013, entire; Bale et
al. 2002, p. 11; Roland and Matter 2016,
p. 22). These climatic changes can also
affect populations indirectly, by altering
resource availability and species
interactions (Service 2018a, p. 36).
Bumble bee abundance for three
species of Bombus in the Rocky
Mountains increased when floral
resources were available for more days,
and the number of days when floral
resources were available increased with
greater summer precipitation and later
snowmelt dates (Ogilvie et al. 2017, p.
4). Several of the targeted Franklin’s
bumble bee and western bumble bee
survey reports between 2015 and 2017
include mention of widespread hot, dry
climate affecting timing and abundance
of floral resources during the surveys
(Bureau of Land Management 2015, p. 2;
Trail 2017, pers. comm.). Although the
Olgilvie et al. study and the survey
reports suggest potential indirect effects
of climate change on Bombus, we have
no information to indicate that the
effects of climate change were
connected to the decline of the
Franklin’s bumble bee; numerous
Bombus species persist in areas that are
considered good quality habitat for the
Franklin’s bumble bee (Pool 2014,
entire; Colyer 2016, entire). As a habitat
generalist, Franklin’s bumble bee
appears to forage on a variety of floral
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resources, and we have no information
to suggest that they would not forage off
of whatever floral resource was in
bloom at the time they emerge from
their nests. We have no information to
suggest that any changes in the
vegetation community to date led to the
decline of the species.
In order to understand the potential
future impact of climate change on
Franklin’s bumble bee, we looked at
climate change projection models.
Global climate projections are
informative and, in some cases, the only
or the best scientific information
available for us to use. However,
projected changes in climate and related
impacts can vary substantially across
and within different regions of the
world (Intergovernmental Panel on
Climate Change 2007, pp. 8–12).
Therefore, we use ‘‘downscaled’’
projections when they are available and
have been developed through
appropriate scientific procedures
because such projections provide
higher-resolution information that is
more relevant to spatial scales used for
analyses of a given species (see Glick et
al. 2011, pp. 58–61, for a discussion of
downscaling).
Downscaled projections as of 2016
were available for our analysis of the
Franklin’s bumble bee from the U.S.
Geological Survey’s National Climate
Change Viewer (Alder, J. and S.
Hostetler. 2016, entire). The National
Climate Change Viewer is based on the
mean of 30 models, which can be used
to predict changes in air temperature
and precipitation for Jackson County,
Oregon (location of the last known
occurrence record of Franklin’s bumble
bee), for two greenhouse gas emission
scenarios, RCP4.5 and RCP8.5. From the
year 2020 to the year 2050, the model
set shows an increase in the mean
maximum air temperature of between
1.9 degrees Fahrenheit (°F) (1 degree
Celsius (°C)) (RCP4.5) and 3.1 °F (1.7 °C)
(RCP8.5), and an increase in the mean
annual minimum air temperature of
between 1.0 °F (0.3 °C) (RCP4.5) and
2.7 °F (1.5 °C) (RCP8.5). For both
scenarios, mean precipitation is
predicted to decrease by approximately
0.4 inches (10 millimeters) for both
scenarios.
Projections for an increase in
temperature and decrease in
precipitation over the next 30 years may
lead to alteration in the vegetation
community in Franklin’s bumble bee
habitat, including the varieties of floral
resources that Franklin’s bumble bee
relies on for nectar. However, we have
no information to suggest that these
changes will result in a decrease in the
availability of nectar resources to the
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species. Some studies suggest that
pollinators are responding to climate
change with recent latitudinal and
elevational range shifts such that there
is spatial mismatch among plants and
their pollinators; while this has been
demonstrated in butterflies, it may be
less of a factor for bumble bees (Service
2018a, p. 36). As generalist foragers,
bumble bees do not require synchrony
with a particular plant species, although
some bumble bee populations are active
earlier in the season than in the past
(Bartomeus et al. 2011, p. 20646).
Projections for an increase in
temperature and decrease in
precipitation over the next 30 years may
also affect the frequency or intensity of
wildfires and storm events (including
flooding). These events could affect the
availability of floral resources, the
suitability of nest locations, and the
survival of overwintering queens.
However, we do not have information
projecting the timing, scope, or intensity
of wildfires or storms; the stochastic
nature of these events limits our ability
to project the magnitude of impact on
the future condition of Franklin’s
bumble bee or its habitat, and hinders
our ability to assess their impact on the
viability of the species.
Summary
Although habitat loss has had
negative effects on bumble bees, we
conclude it is unlikely to be a main
driver of the decline of the Franklin’s
bumble bee. Habitat appears generally
intact and in good condition throughout
the known, historical locations of the
Franklin’s bumble bee and throughout
all of the recent focused survey areas
(with the exceptions of the historical
sites affected by the creation of Lake
Applegate in the fall of 1980, and soil
modification that occurred on a portion
of the Gold Hill site in 2004). In our
assessment, we found no information to
suggest that destruction, degradation, or
conversion of habitat occurred at a
scope and magnitude that would cause
it to be a primary factor in the decline
of the Franklin’s bumble bee (Service
2018a, pp. 35–37). Furthermore, we
have no information to suggest that
habitat destruction or modification will
increase in scope and magnitude to the
point where it will be a primary stressor
to the species in its range in the near
future.
A number of diseases and parasites
are known to occur in bumble bee
populations. These include the
protozoan parasite Crithidia bombi (C.
bombi), the tracheal mite Locustacarus
buchneri, the microsporidium (parasitic
fungus) Nosema bombi (N. bombi), as
well as deformed wing virus. Pathogens
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and parasites are widespread generalists
in the host genus, but affect species
differently according to host
susceptibility and tolerance to infection
(Kissinger et al. 2011, p. 221; Malfi and
Roulston 2014, p. 18). The host species’
life history plays a role in the virulence
of a given pathogen; for instance,
parasites may have relatively smaller
effects on species with shorter colony
life cycles and smaller colony sizes
(Rutrecht and Brown 2009, entire).
Pathogen spillover is a process
whereby parasites and pathogens spread
from commercial bee colonies to native
bee populations (Colla et al. 2006, p.
461; Otterstatter and Thompson 2008, p.
1). The decline of certain Bombus
species from the mid-1990s to present,
particularly species in the subgenus
Bombus sensu stricto (including
Franklin’s bumble bee), was
contemporaneous with the collapse of
commercially bred western bumble bee
(raised primarily to pollinate
greenhouse tomato and sweet pepper
crops beginning in the late 1980s)
(Szabo et al. 2012, pp. 232–233). This
collapse was attributed to infections of
Nosema bombi.
Nosema bombi has been detected in
native bumble bees in North America,
and has been found to be a part of the
natural pathogen load. The fungus has
been reported in Canada since the 1940s
(Cordes et al. 2011, p. 7) and appears to
have a broad host range in North
American (Kissinger et al. 2011, p. 222).
Infections of the pathogen primarily
occur in the malpighian tubules (small
excretory or water regulating glands),
but also in fat bodies, nerve cells, and
sometimes the trachea (Macfarlane et al.
1995). Bombus colonies can appear to
be healthy but still carry N. bombi and
transmit it to other colonies, most likely
when spores are fed to larvae and then
infected adults drift into non-natal
colonies (Service 2018a, p. 25).
While we have no evidence of direct
effects of a virulent strain of N. bombi
on the Franklin’s bumble bee, N. bombi
has been detected in closely related
species in the range of the Franklin’s
bumble bee. Furthermore, N. bombi
infections in rare species like the
Franklin’s bumble bee are more
frequent, are more severe, and seem to
affect a higher percentage of individuals
of the species (Cameron et al. 2011,
entire; Cordes et al. 2011, p. 2).
The effect of pathogens on bumble
bees varies from mild to severe
(Macfarlane et al. 1995; Rutrecht et al.
2007, p. 1719; Otti and Schmid-Hempel
2008, p. 577). Bumble bees infected
with Nosema bombi may have crippled
wings, and queens may have distended
abdomens and be unable to mate (Otti
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and Schmid-Hempel 2007, pp. 122–
123). Malfi and Roulston (2014, p. 24)
found that N. bombi infections are more
frequent and more severe in rare
species, and the species with the highest
percentages of infected individuals were
rare species. Furthermore, the effects of
pathogen infection on bumble bees may
be amplified by other influence factors.
Nutritional stress may compromise the
ability of bumble bees to survive
parasitic infections, as evidenced by a
significant difference in mortality in
bumble bees on a restricted diet
compared to well-fed bees infected with
C. bombi (Brown et al. 2000, pp. 424–
425).
A virulent strain of Nosema bombi
from the buff-tailed bumble bee
(Bombus terrestris) may have spread to
the eastern bumble bee (B. impatiens)
and western bumble bee from Europe. In
the mid-1990s, companies shipped
queen eastern and western bumble bees
to Europe for their development into
colonies to use in commercial
pollination services. When the colonies
had reached sufficient size, they were
shipped back to the United States and
deployed in industrial greenhouse
operations in California, primarily to
pollinate tomatoes and peppers. The
colonies may have picked up N. bombi
prior to their shipment back into the
United States, and once in this country,
the commercially reared colonies may
have spread the virulent strain to wild
populations of Franklin’s bumble bee
(Xerces Society and Thorp 2010, p. 14).
In work partially funded by the Service,
the University of Illinois conducted
surveys for parasites and pathogens in
bumble bee populations of the Pacific
Northwest and Midwest between 2005
and 2009. The goal was to assess
Bombus populations for presence and
prevalence of pathogens, particularly
microsporidia, in an effort to provide
baseline data to assess disease as a
potential factor in the decline of the
Franklin’s bumble bee, western bumble
bee, and American bumble bee (B.
pensylvanicus) (Solter et al. 2010, p. 1).
The highest prevalence of N. bombi was
found in western bumble bee, with 26
percent of collected individuals
infected. Crithidia bombi infections of
western bumble bee were 2.8 percent
overall (Solter et al. 2010, pp. 3–4); no
Franklin’s bumble bees were collected
during the study. However, Mt.
Ashland, Oregon, was one of only three
sites in the Pacific Northwest study area
where N. bombi infections were found
in multiple Bombus species (the
indiscriminate cuckoo bumble bee (B.
insularis) and black-notched bumble bee
(B. bifarius)) (Solter et al. 2010, pp. 3–
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4). Although Cordes et al. (2011, p. 7)
found a new allele in N. bombi, the
recent study by Cameron et al. (2016)
found no evidence of an exotic strain of
N. bombi.
In summary, known pathogens occur
within the historical range of the
Franklin’s bumble bee, and we have
evidence of several pathogens infecting
closely related species within that range
that have also likely affected the
Franklin’s bumble bee. Although we
have no direct evidence of pathogens
playing a role in the decline of the
Franklin’s bumble bee, the
disappearance of the Franklin’s bumble
bee occurred soon after a period of
potential exposure to introduced
pathogens, particularly N. bombi, which
is known to have a more severe impact
on rare species like the Franklin’s
bumble bee. Decline of other closely
related pollinators has been associated
with these pathogens, and it is highly
likely pathogens have had some
negative influence on the resiliency of
Franklin’s bumble bee populations.
Pesticide Use
Exposure to pesticides can occur to
bumble bees from direct spray or drift,
or from gathering or consuming
contaminated nectar or pollen (Johansen
and Mayer 1990; Morandin et al. 2005,
p. 619). Lethal and sublethal effects on
bumble bee eggs, larvae, and adults have
been documented for many different
pesticides under various scenarios
(Service 2018a, p. 28). Documented sublethal effects to individual bumble bees
and colonies include reduced or no
male production, reduced or no egg
hatch, reduced queen production,
reduced queen longevity, reduced
colony weight gain, reduced brood size,
reduced feeding, impaired ovary
development, and an increased number
of foragers or foraging trips or duration
(interpreted as risky behaviors) (Service
2018a, p. 28). Bumble bee habitat can
also be impacted by pesticides due to
changes in vegetation and the removal
or reduction of flowers needed to
provide consistent sources of pollen,
nectar, and nesting material (Service
2018a, p. 28). Declines in bumble bees
in parts of Europe have been at least
partially attributed to the use of
pesticides (Williams 1986, p. 54; Kosior
et al. 2007, p. 81).
Although the use of land for
agricultural purposes has traditionally
involved the use of pesticides and other
products toxic to bees, one particular
class of insecticides known as
neonicotinoids have been strongly
implicated in the decline of honey bees
(Apis spp.) worldwide, and implicated
in the decline of several Bombus
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species, including rusty patched bumble
bee, buff-tailed bumble bee, and eastern
bumble bee (Pisa et al. 2015, p. 69;
Goulson 2013, pp. 7–8; Colla and Packer
2008, p. 10; Lundin et al. 2015, p. 7).
Neonicotinoids are a broad class of
insecticides based on nicotine
compounds used in a variety of
agricultural applications; they act as a
neurotoxin, affecting the central nervous
system of insects by interfering with the
receptors of the insects’ nervous system,
causing overstimulation, paralysis, and
death (Douglas and Tooker 2015, pp.
5090–5092). The neonicotinoid family
of insecticides includes acetamiprid,
clothianidin, imidacloprid, nitenpyram,
nithiazine, thiacloprid, and
thiamethoxam. In the range of the
Franklin’s bumble bee (Jackson,
Douglas, and Josephine Counties in
Oregon, as well as Trinity and Siskiyou
Counties in California), the first
reported use of imidacloprid was in
1996, thiamethoxam in 2001, and
clothianidin in 2004. The use of
neonicotinoid pesticides continued in
the range of the species through 2006,
when the last observation of the
Franklin’s bumble bee was recorded.
Across all five counties, total estimated
applications of these three
neonicotinoids increased from 53.31
pounds (lbs) (24.19 kilograms (kg)) in
1996, to 1,144.6 lbs (519.9 kg) in 2014.
However, the exponential growth of
neonicotinoid applications started in
2011, 5 years after the last observation
of the species. The vast majority of
neonicotinoids are used as seed
treatments on grains and other field
crops (Oregon Department of
Agriculture 2018, pers. comm.), and
total agricultural land within the
historical range of the species is less
than 2 percent of the total land base
(2011 National Land Cover Data Set and
2016 USDA Crop Data Layers (CDL) in
Syngenta 2019, pers. comm).
No studies have investigated the
effects of pesticide use on the Franklin’s
bumble bee, and no discoveries have
been documented of any Franklin’s
bumble bees injured or killed by
pesticides. The Franklin’s bumble bee is
a habitat generalist and is not known to
have a close association with
agricultural lands; therefore, it may have
less exposure to pesticides than some
other Bombus species. However,
pesticide use occurs in the range of the
Franklin’s bumble bee. The similarity in
foraging traits that the Franklin’s
bumble bee has with both honey bees
and the other Bombus species (e.g.,
generalist foragers collecting pollen
from similar food sources) allows us to
infer that Franklin’s bumble bee
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populations are likely to suffer exposure
to and impacts from pesticides in
similar measure to other Bombus
species when the Franklin’s bumble bee
is in areas where pesticides are applied.
Effects of Small Population Size
The Franklin’s bumble bee is rare and
has always had very small populations
(relative to other similar, native bumble
bees in the western United States), and
likely has low genetic diversity due to
the haplodiploid genetic system it
shares with all Bombus species (Zayed
2009, p. 238). These factors make the
species more vulnerable to habitat
change or loss, parasites, diseases,
stochastic events, and other natural
disasters such as droughts (Xerces
Society and Thorp 2010, p. 20). Between
1998 and 2006, the number of Franklin’s
bumble bee observations went from a
high of 98 at 11 locations, to a lone
individual in 2006. No observations of
the Franklin’s bumble bee have
occurred since 2006, despite an increase
in survey effort. Diploid male
production has been detected in
naturally occurring populations of
bumble bees, and recent modeling work
has shown that diploid male production
may initiate a rapid extinction vortex (a
situation in which genetic and
demographic traits and environmental
conditions reinforce each other in a
downward spiral, leading to extinction)
(Goulsen et al. 2008, p. 11.8). Because
of inbreeding and the production of
sterile males, the haplodiploid genetic
system makes bumble bees very
vulnerable when populations get small
(Colla 2018, pers. comm.). Although we
have no direct evidence that small
population size or a rapid extinction
vortex contributed to the decline of the
species, the genetic system and
historically small population size of the
Franklin’s bumble bee likely heightened
the species’ vulnerability to other
threats in the environment; we,
therefore, consider the effects of small
population size a synergistic threat to
the species.
Competition With Nonnative Bees
The European honey bee (Apis
mellifera) was first introduced to eastern
North America in the early 1620s, and
into California in the early 1850s
(Xerces Society and Thorp 2010, p. 21).
The resource needs of the European
honey bee and native Bombus species
may overlap, resulting in the potential
for increased competition for resources
(Thomson 2004, p. 458; Thomson 2006,
p. 407). Decreased foraging activity and
lowered reproductive success of
Bombus colonies have been noted near
European honey bee hives (Evans 2001,
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pp. 32–33; Thomson 2004, p. 458;
Thomson 2006, p. 407). Additionally,
the size of workers of native Bombus
species were noticeably reduced where
European honey bees were present,
which may be detrimental to Bombus
colony success (Goulson and Sparrow
2009, p. 177). It is likely that the effects
discussed in these studies are local in
space and time, and most pronounced
where floral resources are limited and
large numbers of commercial European
honey bee colonies are introduced
(Xerces Society and Thorp 2010, p. 21).
We have no information to indicate that
any area of Franklin’s bumble bee
habitat in the range of the species has
limited floral resources and large
numbers of European honey bees. We
have no information related to the
specific placement of commercial honey
bee colonies in or near Franklin’s
bumble bee habitat. Furthermore,
European honey bees have been present
without noticeable declines in Bombus
populations over large portions of their
ranges (Xerces Society and Thorp 2010,
p. 21), and we have no new information
that connects competition from
European honey bees to the decline of
the Franklin’s bumble bee.
There is potential for nonnative,
commercially raised bumble bees to
naturalize and outcompete native
bumble bees for limited resources such
as nesting sites and forage areas. Five
commercially reared eastern bumble bee
workers and one queen were captured
in the wild near greenhouses where
commercial bumble bees are used,
suggesting this species may have
naturalized outside of its native range.
The eastern bumble bee, which has a
native range in eastern North America,
was detected in western Canada (Ratti
and Colla 2010, pp. 29–31). In Japan,
nonnative buff-tailed bumble bee
colonies founded by bees that had
escaped from commercially produced
colonies had more than four times the
mean reproductive output of native
bumble bees (Matsumura et al. 2004, p.
93). In England, commercially raised
buff-tailed bumble bee colonies had
higher nectar-foraging rates and greater
reproductive output than a native
subspecies of the buff-tailed bumble bee
(Ings et al. 2006, p. 940). Colonies of
eastern bumble bee were imported to
pollinate agricultural crops and
strawberries in Grants Pass, Oregon, in
the range of the Franklin’s bumble bee
(Xerces Society and Thorp 2010, p. 18).
Although nonnative Bombus species
in the range of Franklin’s bumble bee
could outcompete Franklin’s bumble
bee for floral resources and nesting
habitat, we have no information to
definitively connect competition with
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nonnative bumble bees to the decline of
the Franklin’s bumble bee. Furthermore,
invertebrate surveys in Franklin’s
bumble bee habitat continue to show
evidence of healthy populations of other
native Bombus species unaffected by
competition from nonnative bees (Pool
2014, entire; Colyer 2016, entire).
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Summary
We find that several natural and other
human-caused factors contributed to the
decline of the Franklin’s bumble bee.
While it is unlikely that pesticides alone
can account for the decline of the
Franklin’s bumble bee, documented
effects of pesticides on closely related
Bombus species suggest pesticide use
was likely a factor in the decline of the
Franklin’s bumble bee. The
haplodiploid genetic system of the
Franklin’s bumble bee, combined with
its historically small population size,
was also likely a factor in the decline of
the species. Although nonnative
Bombus species in the range of the
Franklin’s bumble bee could
outcompete the Franklin’s bumble bee
for floral resources and nesting habitat,
we have no information connecting
competition with nonnative bumble
bees to the decline of the Franklin’s
bumble bee. Additionally, surveys in
Franklin’s bumble bee habitat continue
to show evidence of healthy populations
of other native Bombus species
unaffected by competition from
nonnative bees.
Synergistic and Cumulative Effects
It is likely that several threats are
acting cumulatively and synergistically
on many Bombus species, including the
Franklin’s bumble bee (Goulson et al.
2015, p. 5), and the combination of
multiple threats is likely more harmful
than any one acting alone (Gill et al.
2012, p. 108; Coors and DeMeester 2008,
p. 1821; Sih et al. 2004, p. 274). There
is recent evidence that the interactive
effects of pesticides and pathogens
could be particularly harmful for
bumble bees (Service 2018a, p. 39).
Nutritional stress may compromise the
ability of bumble bees to survive
parasitic infections (Brown et al. 2000,
pp. 424–425). Bumble bees with
activated immunity may have metabolic
costs, such as increased food
consumption (Tyler et al. 2006, p. 2;
Moret and Schmid-Hempel 2000, pp.
1166–1167). Additionally, exposure to
pesticides may increase with increased
food consumption in infected bees
(Goulson et al. 2015, p. 5). Activating
immunity impairs learning in bumble
bees (Riddell and Mallon 2006;
Alghamdi et al. 2008, p. 480). Impaired
learning is thought to reduce the ability
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of bees to locate floral resources and
extract nectar and pollen, therefore
exacerbating nutritional stresses
(Goulson et al. 2015, p. 5). Further,
declining North American species with
low genetic diversity have higher
prevalence of the pathogen Nosema
bombi (Cameron et al. 2011, p. 665). In
summary, we, therefore, find that
pathogens in combination with
pesticides, as well as pathogens in
combination with the effects of small
population size, may have hastened and
amplified the decline of the Franklin’s
bumble bee to a greater degree than any
one of the three threats would cause on
its own.
Existing Regulatory Mechanisms and
Conservation Efforts
Surveys conducted by Dr. Robbin
Thorp, other private individuals,
university classes and researchers, the
U.S. Forest Service, and Bureau of Land
Management have significantly
contributed to the existing information
on Franklin’s bumble bee. However,
other than those search efforts, we are
aware of no conservation efforts or
beneficial actions specifically taken to
address threats to the Franklin’s bumble
bee. Oregon does not include
invertebrates on their State endangered
species list (Oregon Department of Fish
and Wildlife 2018, entire) and California
has no bee species included on its list
of threatened and endangered
invertebrates (California Department of
Fish and Wildlife 2018, entire).
California has the Franklin’s bumble bee
listed on its list of terrestrial and vernal
pool invertebrates of conservation
priority but has no required actions or
special protections associated with the
listing (California Department of Fish
and Wildlife 2017, p. 10). The
Franklin’s bumble bee is on the species
index for the U.S. Forest Service and
Bureau of Land Management
Interagency Special Status/Sensitive
Species Program (ISSSSP). Although the
Federal agencies include the species in
survey efforts and conduct general
meadow enhancement activities, there
are no actions resulting from the ISSSSP
classification that address known
threats to the Franklin’s bumble bee
(ISSSSP 2018, entire).
General awareness of colony collapse
disorder and increase of conservation
efforts for pollinators in general has
likely had limited, indirect effects on
policies and regulations. The U.S. Forest
Service is working to include a section
in all biological evaluations to address
the effects from agency actions on
pollinators. In addition, the Rogue
River-Siskiyou National Forest is
implementing ongoing projects and
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mitigations to create and enhance
pollinator habitat (Colyer 2018, pers.
comm.). The Oregon Department of
Agriculture restricts some potential
sources of Nosema bombi from entering
the State for agricultural uses, including
commercially produced colonies of
eastern bumble bee; only Bombus
species native to Oregon are allowed for
commercial pollination purposes
(Oregon Department of Agriculture
2017, p. 5). However, California allows,
with appropriate permits, the
importation of eastern bumble bee, and
other species such as the blue orchard
bee (Osmia lignaria), for greenhouse
pollination (California Department of
Food and Agriculture 2017), making the
potential for pathogen spillover from
nonnative bees higher in California.
Some local municipalities in Oregon
enacted legislation against aerial
pesticide applications but none in the
range of the Franklin’s bumble bee
(Powell 2017, p. 1; City of Portland
2015, p. 2). However, in the 2017
legislative session, Oregon passed an
Avoidance of Adverse Effects on
Pollinating Insects law (Oregon Revised
Statutes (ORS) 634.045) that is
providing enhanced training of licensed
and unlicensed pesticide applicators in
the State (Melathopoulos 2018, pers.
comm.), and could thereby reduce
effects of pesticides on pollinators,
including Franklin’s bumble bee.
In January 2017, the U.S.
Environmental Protection Agency’s
Office of Pesticide Programs published
their ‘‘Policy to Mitigate the Acute Risk
to Bees from Pesticide Products,’’ which
recommended new labeling statements
for pesticide products, including
warnings for pesticides with a known
acute toxicity to bees (Tier 1 pesticides),
including neonicotinoids (specifically
including imidacloprid, clothianidin,
and thiamethoxam) (U.S. Environmental
Protection Agency 2017, p. 31). In
addition, the Environmental Protection
Agency is working with State and Tribal
agencies to develop and implement
local pollinator protection plans, known
as Managed Pollinator Protection Plans
(MP3s). The Environmental Protection
Agency is promoting MP3s to address
potential pesticide exposure to bees and
other pollinators at and beyond the site
of the application. However, States and
Tribes have the flexibility to determine
the scope of pollinator protection plans
that best responds to pollinator issues in
their regions. For example, State and
Tribal MP3s may address pesticiderelated risks to all pollinators, including
managed bees and wild insect and noninsect pollinators (U.S. Environmental
Protection Agency 2018). The Service
implemented a ban on the use of
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neonicotinoids on all lands in the
National Wildlife Refuge System in
2014 (Service 2014); however, no refuge
lands occur within the range of the
Franklin’s bumble bee, and the Service
rescinded the ban in 2018 (Service
2018b, entire). None of these
aforementioned regulatory or
conservation measures has appreciably
reduced or fully ameliorated threats to
the Franklin’s bumble bee, as evidenced
by the species’ acute and rangewide
decline.
We note that, by using the SSA
framework to guide our analysis of the
scientific information documented in
the SSA report, we have not only
analyzed individual effects on the
species, but we have also analyzed their
potential cumulative effects. We
incorporate the cumulative effects into
our SSA analysis when we characterize
the current and future condition of the
species. Our assessment of the current
status of the Franklin’s bumble bee
incorporates the threats individually
and cumulatively. Our assessment is
iterative because it accumulates and
evaluates the effects of all the factors
that may be influencing the species,
including threats and conservation
efforts. Because the SSA framework
considers not just the presence of the
factors, but to what degree they
collectively influence risk to the entire
species, our assessment integrates the
cumulative effects of the factors and
replaces a standalone cumulative effects
analysis.
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Summary of Status
The significant decrease in abundance
and distribution of the Franklin’s
bumble bee to date has greatly reduced
the species’ ability to adapt to changing
environmental conditions and to guard
against further losses of adaptive
diversity and potential extinction due to
catastrophic events. It also substantially
reduced the ability of the Franklin’s
bumble bee to withstand environmental
variation, catastrophic events, and
changes in physical and biological
conditions. Coupled with the increased
risk of extirpation due to the interaction
of reduced population size and the
species’ haplodiploid genetic system,
the Franklin’s bumble bee may lack the
resiliency required to sustain
populations into the future, even
without further exposure to pathogens
and pesticides.
Summary of Comments and
Recommendations
In our proposed rule published on
August 13, 2019 (84 FR 40006), we
requested that all interested parties
submit written comments on the
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proposal by October 15, 2019. All
comments we received are posted at
https://www.regulations.gov under
Docket No. FWS–R1–ES–2018–0044.
We contacted appropriate Federal and
State agencies (in both Oregon and
California), scientific experts and
organizations, and other interested
parties and invited them to comment on
the proposal, even if they previously
provided peer or partner review
comments on the SSA report. We did
not receive any additional comments
from individuals or agencies who had
previously provided peer review or
partner review on the SSA report. We
did not receive any requests for a public
hearing. We reviewed all comments for
substantive issues and new information
regarding the Franklin’s bumble bee.
During the comment period, we
received 53 letters or statements directly
addressing the proposed action,
including one comment with 15,749
signatures (supporting the listing of the
Franklin’s bumble bee). All but one of
the commenters supported the listing of
the Franklin’s bumble bee as
endangered. All but one of the
commenters disagreed with our
determination that designating critical
habitat is not prudent. Substantive
comments we received during the
comment period are addressed below
and, where appropriate, are
incorporated directly into this final rule.
Public Comments
(1) Comment: Several commenters
disagreed with our conclusion that
Franklin’s bumble bees are habitat
generalists. Commenters stated that the
limited range of the species
demonstrates that it is only found in
specific habitats and that if the species
was truly a habitat generalist, it would
be expected to have a much larger range.
They noted that the range of the species
is limited to the Siskiyou Mountains, a
subset of the Klamath Mountain region
of southern Oregon and southwestern
California, and that there are specific
characteristics of Franklin’s bumble bee
habitat in that area that can be
identified, such as montane meadows
rich in lupine, California poppy,
mountain monardella, and clover.
Commenters note that the Siskiyou
Range is known for its high number of
endemic species and these other
endemic species are not considered
habitat generalists.
Our Response: As stated in the SSA
report, our analyses are predicated on
multiple assumptions due to the
significant lack of species-specific
information for Franklin’s bumble bee
(2018a, p. 6). We further note that for
the purposes of the analyses in the SSA
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report, we rely heavily on information
from closely-related species from the
same sub-genus, Bombus sensu stricto,
particularly the rusty patched bumble
bee and the western bumble bee. The
range of the western bumble bee
completely overlaps the historical range
of Franklin’s bumble bee, and the
western bumble bee is still found at
several known Franklin’s bumble bee
locations, most recently in 2019 at Mt.
Ashland, the last known location of
Franklin’s bumble bee. As mentioned in
the August 13, 2019, proposed rule (84
FR 40006) and the SSA report, a specific
habitat study for the species has not
been completed, nor have the specific
life-history characteristics and behavior
of this rare species been studied.
Despite uncertainties regarding the
Franklin’s bumble bee’s habitat needs,
we know they need (1) floral resources
for nectaring throughout the colony
cycle, and (2) relatively protected areas
for breeding and shelter. The habitat
elements appearing to fulfill those needs
that have documented use by the
Franklin’s bumble bee are relatively
plentiful and widely distributed.
In our expert elicitation, we asked the
following question: In looking at the
distribution map of all known
occurrences of Franklin’s bumble bee,
are there areas in Douglas, Jackson,
Josephine, Siskiyou, and Trinity
Counties in addition to these occurrence
sites that might contain the species’
known foraging plants: Lupine (Lupinus
spp.), California poppy (Eschscholzia
californica), horsemint or nettle-leaf
giant hyssop (Agastache urticifolia), and
mountain monardella (Monardella
odoratissima)? Dr. Thorp (the
preeminent authority on Franklin’s
bumble bee) responded that he was
‘‘trying to figure out what defined or
limited habitat at the time that [the
species] disappeared.’’ Dr. Thorp noted
that the species had historically ranged
from 500 ft in elevation at Sutherland to
over 6,700 ft at Mt. Shasta and Mt.
Ashland, meaning they could go
through multiple mountain passes to
extend east or south, but they did not;
they were not limited by geography.
Further, they were also not limited by
flowering plants; they are generalist
foragers (Thorp 2018, pers. comm). In
addition, bumble bees ‘‘are classic
generalist foragers, capable of working a
wide variety of plants for their
resources’’ (Williams et al. 2014, p. 15).
The historical record also suggests the
Franklin’s bumble bee may use a variety
of nesting substrates given that a colony
was found in a residential garage in
Medford, Oregon (Thorp 2017, pers.
comm.).
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We agree that the Klamath-Siskiyou
ecoregion, which hosts much of the
historical range of the Franklin’s bumble
bee, is very diverse and relatively rich
in endemic species. The KlamathSiskiyou ecoregion is considered a
global center of biodiversity, is an
International Union for Conservation of
Nature (IUCN) Area of Global Botanical
Significance (1 of 7 in North America),
and is proposed as a World Heritage Site
and United Nations Educational,
Scientific and Cultural Organization
(UNESCO) Biosphere Reserve (World
Wildlife Fund 2020, entire). Extensive
literature is available describing some of
the biologic investigations in this
ecoregion (University of Oregon 2020,
entire). However, we are not aware of
any information linking Franklin’s
bumble bee exclusively to endemic
habitat features, including floral
resources specific to this ecosystem.
(2) Comment: One commenter noted
that forage is only one component of
Franklin’s bumble bee’s niche and does
not alone define a habitat generalist,
citing Devictor et al. 2010. They stated
that even if the species is a general
forager it could still have a relatively
narrow habitat niche, adding that
narrow pollen diets are associated with
other rare bumble bees like Franklin’s
bumble bee. They referenced a recent
study, Wood et al. 2019, that looked at
the diets of two species closely related
to Franklin’s bumble bee, the American
bumble bee and rusty patch bumble bee,
and found these declining species had
a narrow pollen diet, collecting around
one-third fewer pollen types than other
more stable species. The study further
noted that these two species are shorttongued and the anatomical feature was
mentioned as a potential factor in their
narrower diet.
Our Response: There are many factors
related to Franklin’s bumble bees and
their habitat that we do not yet, and may
never, understand; however, the
information gathered for our
assessment, including the opinion of the
preeminent authority on the species (Dr.
Robbin Thorp), indicates that Franklin’s
bumble bee is likely a habitat generalist.
The commenter cites Devictor et al.
2010, when noting forage is only one
component of Franklin’s bumble bee’s
niche and may not alone define a
habitat generalist. However, the same
paper also states that a measure of
ecological specialization is the
assumption that specialists should cooccur with relatively few species; this is
in contrast to generalist species who
should co-occur with many different
species across sites (Devictor et al. 2010,
p. 23), as has been observed with
Franklin’s bumble bees.
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We agree that narrow pollen diets
likely play a role in the decline of some
Bombus species as the distribution and
abundance of their floral resources
change, but we do not have sufficient
information to determine if this was a
significant causal factor in the decline of
the Franklin’s bumble bee. We do have
some records of the species of plants
visited by Franklin’s bumble bee, but we
do not have an exhaustive or
comprehensive list. Of the plants
Franklin’s bumble bee is known to use,
many are widely distributed. For
example, California poppy is found in
Oregon, Washington, Nevada, Arizona,
Minnesota, and northwestern Baja
California, Mexico. Nettle-leaf giant
hyssop (horse mint) is native throughout
western North America from British
Columbia in Canada, to California to
Colorado, where it grows in a wide
variety of habitat types. Mountain
monardella is found in montane forests
between 600 m and 3,100 m (1,969 ft
and 10,170 ft) in elevation in Oregon,
Washington, Nevada, and Utah.
Regarding tongue length, although the
Franklin’s bumble bee is a shorttongued species, Wood et al. found no
evidence of tongue length as a predictor
of dietary breadth (2019, p. 9).
(3) Comment: Several commenters
disagreed that the present or threatened
destruction, modification, or
curtailment of habitat is not a threat to
the Franklin’s bumble bee. One
commenter stated that the Service
analyzed fire suppression, agricultural
intensification, urban development,
livestock grazing, and effects of climate
change, but only as to whether they
contributed to the historical decline of
Franklin’s bumble bee, not as current
threats. One commenter stated that the
climate change effects of increased
drought severity, wildfire risk, and
winter or early season flood risk are
clear threats to Franklin’s bumble bee
habitat in the current and near future;
they noted that flood risk is especially
concerning for overwintering
hibernating queens who may suffer
mortality or respond by emerging too
early for floral resources. The
commenter also noted that due to the
myriad of threats outlined in the August
13, 2019, proposed rule (84 FR 40006),
it is incorrect to conclude that
Franklin’s bumble bee’s habitat is
unlimited in its capacity to provide
uncontaminated resources to the
species. One commenter stated that allterrain vehicle (ATV) use and herbicide
use are current threats to Franklin’s
bumble bee’s habitat, but provided no
additional information upon which to
base those claims.
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Our Response: In our analysis of the
threats facing Franklin’s bumble bee in
the SSA report, we completed a review
of the best available scientific and
commercial information on threats that
have been present in the range of the
bee (Service 2018a, pp. 23–40). During
the public comment period on the
proposed rule we did not receive any
new information regarding potential
threats that prompted us to change the
conclusions in our analysis. The
viability analysis takes into account the
threats to the species that have
influenced historical populations,
threats that are influencing the current
condition of populations, and threats
which are likely to play a role in the
species’ overall viability into the future.
In our SSA report for Franklin’s bumble
bee, we noted those threats that are
likely to play a role in the future
(pathogens, pesticides, and the
synergistic effects of small population
size), but did not complete a full future
condition analysis; the dearth of
information on this species, particularly
the lack of species occurrence
information after 2006, limited our
ability to compare current and future
condition.
Although empirical data are currently
unavailable regarding the level of
habitat loss and degradation specifically
affecting the Franklin’s bumble bee, we
do know that habitat impacts have
caused the decline of other Bombus
species (e.g., Goulson et al. 2015, p. 2;
Goulson and Darvill 2008, pp. 193–194;
Brown and Paxton 2009, pp. 411–412).
Although habitat loss has had negative
effects on Bombus species in general,
available information did not indicate it
was a driver of the decline of Franklin’s
bumble bee. Habitat appears generally
intact and in good condition throughout
the known historical locations of the
Franklin’s bumble bee and in all recent
focused survey areas, and many of these
habitats currently host a wide variety of
other bumble bees, including closelyrelated species like the western bumble
bee. As noted above in Summary of
Biological Status and Threats, we have
no information to suggest that any
known Franklin’s bumble bee locations
were in the path of wildfire at the time
those locations were occupied. Further,
as made evident in our geographic
information system (GIS) analysis, most
of the recent locations with confirmed
Franklin’s bumble bee observations are
on publicly owned land that is managed
to preserve habitat conditions through a
variety of mechanisms, including fire
suppression. Furthermore, we have no
information to suggest that habitat
destruction or modification from fire
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suppression, agricultural intensification,
urban development, and livestock
grazing will increase in intensity to the
point where they will be threats to the
viability of the species in the future
(Bureau of Land Management 2016, p.
103; Portland State University 2015, p.
7; U.S. Forest Service 1989, IV–87 to IV–
90, IV–113 to IV–119; U.S. Forest
Service 1990, pp. 4–149 to 4–179;
Service 2018a, p. 32).
Future changes in temperature and
precipitation may lead to changes in the
vegetation community in Franklin’s
bumble bee habitat. However, as a
habitat generalist, Franklin’s bumble bee
appears to forage on a variety of floral
resources, and we have no information
to suggest that they would not seek the
nectar of whatever floral resource was in
bloom at the time they emerge from
their nests. Additionally, the risk of
catastrophic wildfire and seasonal
flooding, as well as other effects from
storm events, are naturally present in
the ecosystems within the range of the
Franklin’s bumble bee. The effects of
climate change may affect the frequency
and intensity of these events, thereby
affecting the availability of floral
resources, the suitability of nest
locations, and the survival of
overwintering queens. However, we
cannot project the likelihood of when or
where these events will occur, or how
intense they will be if they do occur.
We agree that Franklin’s bumble bee
habitat is not unlimited. As we point
out in the beginning of the SSA report,
Franklin’s bumble bee is the most
narrowly endemic bumble bee in North
America, and possibly the world. In
accordance with listing Franklin’s
bumble bee as endangered under the
Act, we will develop a recovery outline
for this species. Current and possible
future threats will be considered during
recovery planning for this species.
(4) Comment: One commenter
disagreed that critical habitat could not
be defined. They point to our proposed
rule, which states that surveys have
been done in areas that appear to have
good habitat for Bombus and Franklin’s
bumble bee, as evidence that there are
known and defined characteristics of
potential critical habitat in previously
occupied areas.
Our Response: While we acknowledge
that some general habitat associations of
Bombus are known, the Franklin’s
bumble bee has been found in a wide
array of habitat types, from foraging in
montane meadows in a remote
wilderness area of California to nesting
in a residential garage in the city limits
of Medford, Oregon. Furthermore,
elevation does not appear to limit the
species’ dispersal capabilities. No
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habitat study for the Franklin’s bumble
bee has been completed; such a study
was initiated in 2006, when the
Franklin’s bumble bee was last seen, but
could not continue due to the
subsequent absence of the species. As
such, we cannot with specificity
articulate the physical or biological
features essential to the conservation of
the Franklin’s bumble bee, or determine
whether or not any area would meet the
definition of critical habitat for the
Franklin’s bumble bee (see discussion
under Prudency Determination, below).
Even if physical and biological
features can be articulated for the
species, the regulations in effect at the
time the species was proposed for
listing indicated that we may find that
designating critical habitat is not
prudent if it is not beneficial to the
species. With the exception of the
inundation of two sites with older
historical occurrences of Franklin’s
bumble bee locations by the
construction of Applegate Dam, and a
report of soil modification on a portion
of the Gold Hill site 4 years after the last
occurrence of Franklin’s bumble bee in
the area, no noticeable destruction,
modification, or curtailment of habitat
or range can be identified in areas where
the species had been previously located.
No significant destruction or
modification of Franklin’s bumble bee
habitat can be attributed to natural fire,
prescribed fire, agricultural
intensification, urban development,
livestock grazing, or the effects of
climate change. Additionally, as
discussed above, the Franklin’s bumble
bee has been documented using a wide
variety of habitats throughout its range.
Because habitat for the Franklin’s
bumble bee is not limiting, and because
the bee is considered to be flexible with
regards to its habitat, the availability of
habitat does not limit the conservation
of the Franklin’s bumble bee now, nor
will it in the future (see response to
Comment (3)). Therefore, we have
determined that designation of critical
habitat for the Franklin’s bumble bee is
not beneficial to the species and,
therefore, not prudent.
(5) Comment: Two commenters
disagreed that the designation of critical
habitat would not be beneficial to the
conservation of the species. They argue
it would be beneficial due to the
following: (1) Critical habitat would
promote connectivity between habitat
patches, which will help reduce the risk
of inbreeding depression and promote
recovery of the species; (2) many studies
have shown the link between quality
habitat and nutrition and health of
bumble bee colonies, and critical habitat
would be beneficial because it would
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give Franklin’s bumble bee access to
more high-quality habitat to combat the
threats of pathogens and pesticides and
to recover from them; (3) competition
and disease from nonnative honey bees,
as well as pesticides from both
agriculture and siliviculture, are threats
that will be unregulated without the
designation of critical habitat; (4)
critical habitat would provide concrete
objective locations in which to protect
the species through section 7 of the Act;
and (5) critical habitat would inform the
species recovery plan and where exactly
the Service would implement recovery
actions to ameliorate threats to the
species.
Our Response: The implementing
regulations of the Act upon which the
August 13, 2019, proposed rule (84 FR
40006) and this final rule are based set
forth that the factors the Service may
consider in determining that a critical
habitat designation would not be
prudent include, but are not limited to,
whether the species is threatened by
taking or other human activity, and
identification of critical habitat can be
expected to increase the degree of threat
to the species; or whether such
designation of critical habitat would not
be beneficial to the species (50 CFR
424.12(a)(1)). We determine that the
designation of critical habitat would not
be beneficial to the species because the
present or threatened destruction,
modification, or curtailment of the
species’ habitat or range (Factor A) is
not a threat to the Franklin’s bumble bee
and because we cannot with specificity
articulate the physical or biological
features essential to the conservation of
the Franklin’s bumble bee, or determine
whether or not any area would meet the
definition of critical habitat for the
Franklin’s bumble bee (see discussion
under Prudency Determination, below).
As mentioned in our response to
Comments (3) and (4), no noticeable
destruction, modification, or
curtailment of Franklin’s bumble bee
habitat or range can be identified in
areas where the species had been
previously located, and could not be
shown to have affected the resiliency of
any population of Franklin’s bumble
bee. None of the potential threats to
Franklin’s bumble bee habitat we
assessed appears to threaten the
viability of the species (USFWS 2018a,
pp. 23–41). Therefore, we find that
because the present or threatened
destruction, modification, or
curtailment of a species’ habitat or range
is not a threat to Franklin’s bumble bee,
designating critical habitat is not
beneficial and, therefore, not prudent.
Furthermore, regarding section 7
consultation, because of the listing of
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the species (absent critical habitat),
Federal agencies will still be required to
consult under section 7 of the Act on
activities that may affect this species in
areas where the Franklin’s bumble bee
is reasonably certain to occur. The
Federal action agency will be required
to identify any listed species that could
be within the project area of any
proposed activity, and consult with the
Service if that activity is likely to
adversely affect the species.
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Determination of the Status of
Franklin’s Bumble Bee
Section 4 of the Act (16 U.S.C. 1533)
and its implementing regulations (50
CFR part 424) set forth the procedures
for determining whether a species meets
the definition of an endangered species
or a threatened species. The Act defines
an ‘‘endangered species’’ as a species
that is ‘‘in danger of extinction
throughout all or a significant portion of
its range,’’ and a ‘‘threatened species’’ as
a species that is ‘‘likely to become an
endangered species within the
foreseeable future throughout all or a
significant portion of its range.’’ The Act
requires that we determine whether a
species meets the definition of
‘‘endangered species’’ or ‘‘threatened
species’’ because of any of the following
factors: (A) The present or threatened
destruction, modification, or
curtailment of its habitat or range; (B)
overutilization for commercial,
recreational, scientific, or educational
purposes; (C) disease or predation; (D)
the inadequacy of existing regulatory
mechanisms; or (E) other natural or
manmade factors affecting its continued
existence.
Status Throughout All of Its Range
We evaluated the past, present, and
future threats to the Franklin’s bumble
bee and assessed the cumulative effect
of the threats under the Act’s section
4(a)(1) factors. Our assessment did not
find habitat loss or modification (Factor
A) to be the cause of the decline of the
Franklin’s bumble bee, and we have no
information to suggest that habitat
destruction or modification will
increase in intensity in the near future.
There is no indication that the
Franklin’s bumble bee was at risk of
overutilization for commercial,
recreational, scientific, or educational
purposes (Factor B). Known pathogens
occur within the historical range of the
Franklin’s bumble bee, and we have
evidence of several pathogens (Factor C)
infecting closely related species within
that range. Although we do not have
direct evidence of pathogens playing a
role in the decline of the Franklin’s
bumble bee, the disappearance of the
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Franklin’s bumble bee occurred soon
after a period of introduction of new
pathogens. Furthermore, documented
effects to other closely related species
lead many species experts to suspect
that the effects of pathogens had some
connection to the decline of the
Franklin’s bumble bee. We evaluated
existing regulatory mechanisms (Factor
D) and conservation measures and their
effects on the threats and the status of
the Franklin’s bumble bee; we found
that the existing regulatory mechanisms
or conservation measures in place do
not appreciably reduce or ameliorate the
existing threats to the species, as
evidenced by the species’ acute and
rangewide decline. Although we have
no direct evidence that pesticide use
contributed to the decline of the
Franklin’s bumble bee, confirmed
effects to other closely related Bombus
species suggest that pesticide use
(Factor E) was likely a factor in the
decline of the Franklin’s bumble bee.
Additionally, given the historically
small population size (Factor E) of the
Franklin’s bumble bee and its
haplodiploid genetic system, it is more
vulnerable to extirpation than other
species, and it is likely the genetic
system and the rarity of this species
contributed to the decline of the
Franklin’s bumble bee (Factor E).
The combination of multiple threats is
typically more harmful than any one
acting alone, and it is likely that several
of the threats mentioned above acted
cumulatively and synergistically on the
Franklin’s bumble bee. Pathogens in
combination with pesticides, as well as
pathogens in combination with the
effects of small population size, may
have hastened and amplified the decline
of the Franklin’s bumble bee to a greater
degree than any one of the three factors
caused on its own. Although the
ultimate source of the decline is
unknown, the acute and rangewide
decline of the Franklin’s bumble bee is
undisputable.
The Act defines an ‘‘endangered
species’’ as any species that is in danger
of extinction throughout all or a
significant portion of its range, and a
‘‘threatened species’’ as any species that
is likely to become endangered within
the foreseeable future throughout all or
a significant portion of its range. We
find that, based on the severity and
immediacy of threats currently affecting
the species, the Franklin’s bumble bee
meets the definition of an endangered
species. The threats of pathogens,
pesticides, and small population size
are ongoing and rangewide; they will
continue to act individually and in
combination to decrease the resiliency,
redundancy, and representation of the
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Franklin’s bumble bee. The risk of
extinction is high because the species
has not been found since 2006, and the
suspected threats to the species persist.
We find that a threatened species status
is not appropriate for the Franklin’s
bumble bee because of the extreme loss
of abundance of the species, because the
threats are occurring rangewide and are
not localized, and because the threats
are ongoing and expected to continue
into the future. Thus, after assessing the
best available information, we
determine that the Franklin’s bumble
bee is in danger of extinction
throughout all of its range.
Status Throughout a Significant Portion
of Its Range
Under the Act and our implementing
regulations, a species may warrant
listing if it is in danger of extinction or
likely to become so in the foreseeable
future throughout all or a significant
portion of its range. We have
determined that the Franklin’s bumble
bee is in danger of extinction
throughout all of its range and
accordingly did not undertake an
analysis of whether there are any
significant portions of its range. Because
Franklin’s bumble bee warrants listing
as endangered throughout all of its
range, our determination is consistent
with the decision in Center for
Biological Diversity v. Everson, 2020 WL
437289 (D.D.C. Jan. 28, 2020), in which
the court vacated only the aspect of our
July 1, 2014, Final Policy on
Interpretation of the Phrase ‘‘Significant
Portion of Its Range’’ in the Endangered
Species Act’s Definitions of
‘‘Endangered Species’’ and ‘‘Threatened
Species’’ (79 FR 37578) that provided
the Services do not undertake an
analysis of significant portions of a
species’ range if the species warrants
listing as threatened throughout all of its
range.
Determination of Status
Our review of the best available
scientific and commercial information
indicates that the Franklin’s bumble bee
meets the definition of an endangered
species. Therefore, we are listing the
Franklin’s bumble bee as an endangered
species in accordance with sections 3(6)
and 4(a)(1) of the Act. Although this
species has not been observed since
2006, we conclude it is premature at
this time to determine that the species
is extinct absent a more thorough survey
effort. We recommend expanded survey
efforts to help verify the status of this
species.
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Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened species under the Act
include recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness, and conservation by
Federal, State, Tribal, and local
agencies; private organizations; and
individuals. The Act encourages
cooperation with States and other
countries and calls for recovery actions
to be carried out for listed species. The
protection required by Federal agencies
and the prohibitions against certain
activities are discussed, in part, below.
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Recovery Actions
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Subsection 4(f) of
the Act calls for the Service to develop
and implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse a species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, selfsustaining, and functioning components
of their ecosystems.
Recovery planning includes the
development of a recovery outline
shortly after a species is listed, and
preparation of a draft and final recovery
plan. The recovery outline guides the
immediate implementation of urgent
recovery actions and describes the
process we will use to develop a
recovery plan. Revisions of the plan
may be done to address continuing or
new threats to the species, as new
substantive information becomes
available. The recovery plan also
identifies recovery criteria for review of
when a species may be ready for
reclassification from endangered to
threatened (‘‘downlisting’’) or removal
from protected status (‘‘delisting’’), and
methods for monitoring recovery
progress. Recovery plans also establish
a framework for agencies to coordinate
their recovery efforts and provide
estimates of the cost of implementing
recovery tasks. Recovery teams
(composed of species experts, Federal
and State agencies, nongovernmental
organizations, and stakeholders) are
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often established to develop recovery
plans. When completed, the recovery
outline, draft recovery plan, and the
final recovery plan will be available on
our website (https://www.fws.gov/
endangered), or from our Oregon Fish
and Wildlife Office (see FOR FURTHER
INFORMATION CONTACT).
Implementation of recovery actions
generally requires the participation of a
broad range of partners, including other
Federal agencies, States, Tribes,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private, State, and tribal lands.
Following publication of this final
listing rule, funding for recovery actions
will be available from a variety of
sources, including Federal budgets,
State programs, and cost share grants for
non-Federal landowners, the academic
community, and nongovernmental
organizations. In addition, pursuant to
section 6 of the Act, the States of Oregon
and California will be eligible for
Federal funds to implement
management actions that promote the
protection or recovery of the Franklin’s
bumble bee. Information on our grant
programs that are available to aid
species recovery can be found at: https://
www.fws.gov/grants.
Please let us know if you are
interested in participating in recovery
efforts for the Franklin’s bumble bee.
Additionally, we invite you to submit
any new information on this species
whenever it becomes available and any
information you may have for recovery
planning purposes (see FOR FURTHER
INFORMATION CONTACT).
Regulatory Provisions
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as an endangered
or threatened species and with respect
to its critical habitat, if any is
designated. Regulations implementing
this interagency cooperation provision
of the Act are codified at 50 CFR part
402. Section 7(a)(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 any endangered or
threatened species or destroy or
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adversely modify its critical habitat. If a
Federal action may affect a listed
species or its critical habitat, the
responsible Federal agency must enter
into consultation with the Service.
Federal agency actions within the
species’ habitat that may require
conference or consultation or both
include management and any other
landscape-altering activities on Federal
lands administered by the U.S. Forest
Service and Bureau of Land
Management, the National Park Service,
and the Bureau of Reclamation;
technical assistance and projects funded
through the U.S. Department of
Agriculture Natural Resources
Conservation Service; issuance of
section 404 Clean Water Act (33 U.S.C.
1251 et seq.) permits by the U.S. Army
Corps of Engineers, and construction
and maintenance of roads or highways
by the Federal Highway Administration.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to endangered wildlife. The prohibitions
of section 9(a)(1) of the Act, codified at
50 CFR 17.21, make it illegal for any
person subject to the jurisdiction of the
United States to take (which includes
harass, harm, pursue, hunt, shoot,
wound, kill, trap, capture, or collect; or
to attempt any of these) endangered
wildlife within the United States or on
the high seas. In addition, it is unlawful
to import; export; deliver, receive, carry,
transport, or ship in interstate or foreign
commerce in the course of commercial
activity; or sell or offer for sale in
interstate or foreign commerce any
species listed as an endangered species.
It is also illegal to possess, sell, deliver,
carry, transport, or ship any such
wildlife that has been taken illegally.
Certain exceptions apply to employees
of the Service, the National Marine
Fisheries Service, other Federal land
management agencies, and State
conservation agencies.
We may issue permits to carry out
otherwise prohibited activities
involving endangered wildlife under
certain circumstances. Regulations
governing permits are codified at 50
CFR 17.22. With regard to endangered
wildlife, a permit may be issued for the
following purposes: For scientific
purposes, to enhance the propagation or
survival of the species, and for
incidental take in connection with
otherwise lawful activities. There are
also certain statutory exemptions from
the prohibitions, which are found in
sections 9 and 10 of the Act.
It is our policy, as published in the
Federal Register on July 1, 1994 (59 FR
34272), to identify to the maximum
extent practicable at the time a species
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is listed, those activities that would or
would not constitute a violation of
section 9 of the Act. The intent of this
policy is to increase public awareness of
the effect of a listing on proposed and
ongoing activities within the range of
the listed species. Based on the best
available information, the following
actions are unlikely to result in a
violation of section 9 of the Act if these
activities are carried out in accordance
with existing regulations and permit
requirements; this list is not
comprehensive:
(1) Recreation, specifically skiing at
Mt. Ashland, and use of the Pacific
Crest Trail;
(2) Timber sales; and
(3) Livestock grazing.
Based on the best available
information, the following actions may
potentially result in a violation of
section 9 of the Act if they are not
authorized in accordance with
applicable law; this list is not
comprehensive:
(1) Unauthorized handling or
collecting of the Franklin’s bumble bee;
(2) Unauthorized release of biological
control agents that attack any life stage
of the Franklin’s bumble bee, including
the unauthorized use of herbicides,
pesticides, or other chemicals in areas
in which the Franklin’s bumble bee is
known to occur (i.e., in the Franklin’s
bumble bee’s historical range); and
(3) Unauthorized release of nonnative
species or native species that carry
pathogens, diseases, or fungi that are
known or suspected to adversely affect
the Franklin’s bumble bee where the
species is known to occur (i.e., in the
Franklin’s bumble bee’s historical
range).
Questions regarding whether specific
activities would constitute a violation of
section 9 of the Act should be directed
to the Oregon Fish and Wildlife Office
(see FOR FURTHER INFORMATION CONTACT).
II. Critical Habitat
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Background
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
(a) Essential to the conservation of the
species, and
(b) Which may require special
management considerations or
protection; and
(2) Specific areas outside the
geographical area occupied by the
species at the time it is listed, upon a
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determination that such areas are
essential for the conservation of the
species.
Our regulations at 50 CFR 424.02
define ‘‘geographical area occupied by
the species’’ as an area that may
generally be delineated around species’
occurrences, as determined by the
Secretary (i.e., range). Such areas may
include those areas used throughout all
or part of the species’ life cycle, even if
not used on a regular basis (e.g.,
migratory corridors, seasonal habitats,
and habitats used periodically, but not
solely by vagrant individuals).
Conservation, as defined under
section 3 of the Act, means to use and
the use of all methods and procedures
that are necessary to bring an
endangered or threatened species to the
point at which the measures provided
pursuant to the Act are no longer
necessary. Such methods and
procedures include, but are not limited
to, all activities associated with
scientific resources management such as
research, census, law enforcement,
habitat acquisition and maintenance,
propagation, live trapping, and
transplantation, and, in the
extraordinary case where population
pressures within a given ecosystem
cannot be otherwise relieved, may
include regulated taking.
Critical habitat receives protection
under section 7 of the Act through the
requirement that Federal agencies
ensure, in consultation with the Service,
that any action they authorize, fund, or
carry out is not likely to result in the
destruction or adverse modification of
critical habitat. The designation of
critical habitat does not affect land
ownership or establish a refuge,
wilderness, reserve, preserve, or other
conservation area. Such designation
does not allow the government or public
to access private lands. Such
designation does not require
implementation of restoration, recovery,
or enhancement measures by nonFederal landowners. Where a landowner
requests Federal agency funding or
authorization for an action that may
affect a listed species or critical habitat,
the Federal agency would be required to
consult with the Service under section
7(a)(2) of the Act. However, even if the
Service were to conclude that the
proposed activity would result in
destruction or adverse modification of
the critical habitat, the Federal action
agency and the landowner are not
required to abandon the proposed
activity, or to restore or recover the
species; instead, they must implement
‘‘reasonable and prudent alternatives’’
to avoid destruction or adverse
modification of critical habitat.
PO 00000
Frm 00028
Fmt 4700
Sfmt 4700
Under the first prong of the Act’s
definition of critical habitat, areas
within the geographical area occupied
by the species at the time it was listed
are included in a critical habitat
designation if they contain physical or
biological features (1) which are
essential to the conservation of the
species and (2) which may require
special management considerations or
protection. For these areas, critical
habitat designations identify, to the
extent known using the best scientific
and commercial data available, those
physical or biological features that are
essential to the conservation of the
species (such as space, food, cover, and
protected habitat). In identifying those
physical or biological features within an
area, we focus on the specific features
that support the life-history needs of the
species, including, but not limited to,
water characteristics, soil type,
geological features, prey, vegetation,
symbiotic species, or other features. A
feature may be a single habitat
characteristic, or a more complex
combination of habitat characteristics.
Features may include habitat
characteristics that support ephemeral
or dynamic habitat conditions. Features
may also be expressed in terms relating
to principles of conservation biology,
such as patch size, distribution
distances, and connectivity.
Under the second prong of the Act’s
definition of critical habitat, we can
designate critical habitat in 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. We determine whether
unoccupied areas are essential for the
conservation of the species by
considering the life-history, status, and
conservation needs of the species. This
is further informed by any generalized
conservation strategy, criteria, or outline
that may have been developed for the
species to provide a substantive
foundation for identifying which
features and specific areas are essential
to the conservation of the species and,
as a result, to the development of the
critical habitat designation. For
example, an area currently occupied by
the species but that was not occupied at
the time of listing may be essential to
the conservation of the species and may
be included in the critical habitat
designation.
Section 4 of the Act requires that we
designate critical habitat on the basis of
the best scientific data available.
Further, our Policy on Information
Standards Under the Endangered
Species Act (published in the Federal
Register on July 1, 1994 (59 FR 34271)),
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the Information Quality Act (section 515
of the Treasury and General
Government Appropriations Act for
Fiscal Year 2001 (Pub. L. 106–554; H.R.
5658)), and our associated Information
Quality Guidelines, provide criteria,
establish procedures, and provide
guidance to ensure that our decisions
are based on the best scientific data
available. They require our biologists, to
the extent consistent with the Act and
with the use of the best scientific data
available, to use primary and original
sources of information as the basis for
recommendations to designate critical
habitat.
Prudency Determination
Section 4(a)(3) of the Act, as
amended, and implementing regulations
(50 CFR 424.12), require that, to the
maximum extent prudent and
determinable, the Secretary shall
designate critical habitat at the time the
species is determined to be an
endangered or threatened species.
On August 27, 2019, the Service
published a final rule (84 FR 45020)
revising the regulations at 50 CFR part
424 for listing species and designating
critical habitat. However, the revisions
apply only to relevant rulemakings for
which the proposed rule is published
after September 26, 2019, the effective
date of the final rule. Thus, the prior
version of the regulations at 50 CFR part
424 continues to apply to any
rulemakings for which a proposed rule
was published before September 26,
2019, including this final rule for
Franklin’s bumble bee.
The prior version of the regulations at
50 CFR part 424 (50 CFR 424.12(a)(1))
state that the designation of critical
habitat is not prudent when one or both
of the following situations exist:
(1) The species is threatened by taking
or other human activity, and
identification of critical habitat can be
expected to increase the degree of threat
to the species, or
(2) Such designation of critical habitat
would not be beneficial to the species.
In determining whether a designation
would not be beneficial, the factors the
Services may consider includes whether
the present or threatened destruction,
modification, or curtailment of a
species’ habitat or range is not a threat
to the species.
As discussed above in the threats
analysis, there is currently no imminent
threat of take attributed to collection or
vandalism identified under Factor B for
this species, and identification and
mapping of critical habitat is not
expected to initiate any such threat. In
the absence of finding that the
designation of critical habitat would
VerDate Sep<11>2014
15:55 Aug 23, 2021
Jkt 253001
increase threats to a species, we next
determine whether such designation of
critical habitat would be beneficial to
the Franklin’s bumble bee. For the
reasons discussed below, we have
determined that designating critical
habitat would not be beneficial.
Designating Habitat Would Not Be
Beneficial to the Species
The Franklin’s bumble bee was
widely distributed throughout its range
and considered flexible with regard to
habitat requirements. We know that the
Franklin’s bumble bee needs (1) floral
resources for nectaring throughout the
colony cycle, and (2) relatively
protected areas for breeding and shelter.
In addition, because the best available
scientific information indicates that the
Franklin’s bumble bee is a generalist
forager, its habitat preferences and
needs are relatively plentiful and widely
distributed. While Bombus species in
general might prefer protected meadows
with an abundance of wildflowers, the
Franklin’s bumble bee has been found
in a wide array of habitat types, from
foraging in montane meadows in a
remote wilderness area of California to
nesting in a residential garage in the city
limits of Medford, Oregon. The species
has a broad elevational range from 162
m (540 ft) to 2,340 m (7,800 ft);
elevation does not appear to limit the
species’ dispersal capabilities.
Some general habitat associations of
Bombus are known; however, as one of
the rarest Bombus species, the
Franklin’s bumble bee is somewhat
enigmatic and a specific habitat study
for the Franklin’s bumble bee has not
been completed. Such a study was
initiated in 2006, when the Franklin’s
bumble bee was last seen, but could not
continue due to the subsequent absence
of the species. Therefore, we cannot
with specificity articulate the physical
or biological features essential to the
conservation of the Franklin’s bumble
bee, or determine whether or not any
area would meet the definition of
critical habitat for the Franklin’s bumble
bee.
Since it was first identified in 1921,
the Franklin’s bumble bee appears to
have always been a rare species with a
limited range. In fact, the species has
perhaps the most limited range of any
Bombus species in the world.
Nonetheless, Franklin’s bumble bee
habitat is not known to be limiting, and
habitat loss is not a threat to the species.
With the exception of the inundation of
two sites with older historical
occurrences of Franklin’s bumble bee
(through the construction of Applegate
Dam, and a report of soil modification
on a portion of the Gold Hill site 4 years
PO 00000
Frm 00029
Fmt 4700
Sfmt 4700
47237
after the last occurrence of Franklin’s
bumble bee in the area), no noticeable
destruction, modification, or
curtailment of habitat or range can be
identified in areas where the species
had been previously located. No
significant destruction or modification
of Franklin’s bumble bee habitat can be
attributed to natural fire, prescribed fire,
agricultural intensification, urban
development, livestock grazing, or the
effects of climate change. Additionally,
as discussed above, the Franklin’s
bumble bee has been documented using
a wide variety of habitats throughout its
range. Because habitat for the Franklin’s
bumble bee is not limiting, and because
the bee is considered to be flexible with
regards to its habitat, the availability of
habitat does not limit the conservation
of the Franklin’s bumble bee now, nor
will it in the foreseeable future.
In the Service and National Marine
Fisheries Service’s response to
comments on the February 11, 2016,
final rule (81 FR 7414) revising the
critical habitat regulations (the
regulations in effect at the time the
Franklin’s bumble bee was proposed for
listing), the Services expressly
contemplated a fact pattern where
designating critical habitat may not be
beneficial to the species: ‘‘[I]n some
circumstances, a species may be listed
because of factors other than threats to
its habitat or range, such as disease, and
the species may be a habitat generalist.
In such a case, on the basis of the
existing and revised regulations, it is
permissible to determine that critical
habitat is not beneficial and, therefore,
not prudent’’ (81 FR 7425). This is the
fact pattern we are presented with in the
case of the Franklin’s bumble bee. In
view of the foregoing, we conclude that
present or threatened destruction,
modification, or curtailment of habitat is
not a threat to the Franklin’s bumble
bee; rather, disease and other manmade
factors are likely the primary threat to
the species within its habitat. Therefore,
in accordance with 50 CFR 424.12(a)(1),
we determine that critical habitat is not
beneficial and, therefore, not prudent
for the Franklin’s bumble bee.
Required Determinations
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act
(NEPA; 42 U.S.C. 4321 et seq.), need not
be prepared in connection with listing
a species as an endangered or
threatened species under the
E:\FR\FM\24AUR1.SGM
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47238
Federal Register / Vol. 86, No. 161 / Tuesday, August 24, 2021 / Rules and Regulations
Endangered Species Act. We published
a notice outlining our reasons for this
determination in the Federal Register
on October 25, 1983 (48 FR 49244).
Government-To-Government
Relationship With Tribes
In accordance with the President’s
memorandum of April 29, 1994
(Government-to-Government Relations
with Native American Tribal
Governments; 59 FR 22951), Executive
Order 13175 (Consultation and
Coordination With Indian Tribal
Governments), and the Department of
the Interior’s manual at 512 DM 2, we
acknowledge our responsibility to
communicate meaningfully with
recognized Federal Tribes on a
government-to-government basis. In
accordance with Secretarial Order 3206
of June 5, 1997 (American Indian Tribal
Rights, Federal-Tribal Trust
Responsibilities, and the Endangered
Species Act), we acknowledge our
responsibilities to work directly with
tribes in developing programs for
healthy ecosystems, to acknowledge that
tribal lands are not subject to the same
controls as Federal public lands, to
remain sensitive to Indian culture, and
Common name
*
INSECTS
Bee, bumble, Franklin’s ..
*
*
References Cited
A complete list of references cited in
this rule is available on the internet at
https://www.regulations.gov under
Docket No. FWS–R1–ES–2018–0044 and
upon request from the Oregon Fish and
Wildlife Office (see FOR FURTHER
INFORMATION CONTACT).
■
Authors
The primary authors of this rule are
the staff members of the Fish and
Wildlife Service’s Species Assessment
Team and the Oregon Fish and Wildlife
Office.
Where listed
*
Bombus franklini .............
*
BILLING CODE 4333–15–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 300
[Docket No.: 210415–0082]
Wherever found ..............
E .........
*
Jkt 253001
This document announces
two additional season dates of August
27 and September 24 for the
Washington South Coast and Columbia
River subareas for Pacific halibut
recreational fisheries in the
International Pacific Halibut
Commission’s regulatory Area 2A off
Washington, Oregon, and California.
This action is intended to conserve
Pacific halibut and provide angler
opportunity where available.
SUMMARY:
Submit your comments,
identified by NOAA–NMFS–2020–0157,
by either of the following methods:
• Federal e-Rulemaking Portal: Go to
www.regulations.gov/docket/NOAANMFS-2020-0157, click the ‘‘Comment’’
Fmt 4700
1. The authority citation for part 17
continues to read as follows:
AUTHORITY: 16 U.S.C. 1361–1407; 1531–
1544; and 4201–4245, unless otherwise
noted.
2. Amend § 17.11 in paragraph (h) by
adding an entry for ‘‘Bee, bumble,
Franklin’s’’ to the List of Endangered
and Threatened Wildlife in alphabetical
order under INSECTS to read as follows:
■
§ 17.11 Endangered and threatened
wildlife.
*
*
*
(h) * * *
Sfmt 4700
*
*
*
85 FR [Insert Federal Register page where the
document begins], 8/24/21.
Temporary rule; inseason
adjustment; request for comments.
Frm 00030
PART 17—ENDANGERED AND
THREATENED WILDLIFE AND PLANTS
*
ACTION:
PO 00000
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as set forth
below:
*
ADDRESSES:
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
AGENCY:
Regulation Promulgation
*
This action is effective August
20, 2021, through September 30, 2021.
Submit comments on or before
September 8, 2021.
Pacific Halibut Fisheries; Catch
Sharing Plan; Inseason Action
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Listing citations and applicable rules
DATES:
RTID 0648–XB316
15:55 Aug 23, 2021
Status
*
*
[FR Doc. 2021–17832 Filed 8–23–21; 8:45 am]
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List of Subjects in 50 CFR Part 17
Scientific name
Martha Williams,
Principal Deputy Director, Exercising the
Delegated Authority of the Director, U.S. Fish
and Wildlife Service.
VerDate Sep<11>2014
to make information available to tribes.
On July 17, 2017, as part of our status
review process, we sent out notification
letters to 11 Tribes that are in proximity
to the known historical range of the
Franklin’s bumble bee (6 Tribes in
Oregon and 5 Tribes in California). The
letter provided the Tribes early
notification that were conducting a
status review for Franklin’s bumble bee
and solicited their input to ensure that
we had the best scientific data available
to inform our subsequent finding on the
status. We did not receive a response
from any of the Tribes.
*
*
icon, complete the required fields, and
enter or attach your comments.
• Mail: Submit written comments to
Barry Thom, c/o Kathryn Blair, West
Coast Region, NMFS, 1201 NE Lloyd
Blvd., Suite 1100, Portland, OR 97232.
Instructions: NMFS may not consider
comments if they are sent by any other
method, to any other address or
individual, or received after the
comment period ends. All comments
received are a part of the public record
and NMFS will post them for public
viewing on www.regulations.gov
without change. All personal identifying
information (e.g., name, address, etc.),
confidential business information, or
otherwise sensitive information
submitted voluntarily by the sender is
publicly accessible. NMFS will accept
anonymous comments (enter ‘‘N/A’’ in
the required fields if you wish to remain
anonymous).
Docket: This rule is accessible via the
internet at the Office of the Federal
Register website at https://
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Agencies
[Federal Register Volume 86, Number 161 (Tuesday, August 24, 2021)]
[Rules and Regulations]
[Pages 47221-47238]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-17832]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R1-ES-2018-0044; FF09E21000 FXES11110900000 212]
RIN 1018-BD25
Endangered and Threatened Wildlife and Plants; Endangered Species
Status for Franklin's Bumble Bee
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), are listing
the Franklin's bumble bee (Bombus franklini), an invertebrate species
from Douglas, Jackson, and Josephine Counties in Oregon, and Siskiyou
and Trinity Counties in California, as an endangered species under the
Endangered Species Act of 1973, as amended (Act). This rule adds this
species to the Federal List of Endangered and Threatened Wildlife and
applies the protections of the Act to this species. We are not
designating critical habitat for the Franklin's bumble bee because we
determined that such a designation would not be beneficial to the
species.
DATES: This rule is effective September 23, 2021.
ADDRESSES: This final rule and supporting documents are available on
the internet at https://www.regulations.gov in Docket No. FWS-R1-ES-
2018-0044, or at https://ecos.fws.gov.
FOR FURTHER INFORMATION CONTACT: Paul Henson, Field Supervisor, U.S.
Fish and Wildlife Service, Oregon Fish and Wildlife Office, 2600 SE
98th Ave., Suite 100, Portland, OR 97266; telephone 503-231-6179.
Persons who use a telecommunications device for the deaf (TDD) may call
the Federal Relay Service at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. Under the Act, if we determine that
a species may be an endangered or threatened species throughout all or
a significant portion of its range, we are required to promptly publish
a proposal in the Federal Register and make a determination on our
proposal within 1 year. To the maximum extent prudent and determinable,
we must designate critical habitat for any species that we determine to
be an endangered or threatened species under the Act. Listing a species
as an endangered or threatened species and designation of critical
habitat can only be completed by issuing a rule.
What this document does. This rule lists Franklin's bumble bee
(Bombus franklini) as an endangered species under the Act. We are not
designating critical habitat because we determined that a designation
is not prudent for this species.
The basis for our action. Under the Act, we may determine that a
species is an endangered or threatened species because of any of five
factors: (A) The present or threatened destruction, modification, or
curtailment of its habitat or range; (B) overutilization for
commercial, recreational, scientific, or educational purposes; (C)
disease or predation; (D) the inadequacy of existing regulatory
mechanisms; or (E) other natural or manmade factors affecting its
continued existence. We have determined that Franklin's bumble bee
meets the definition of an endangered species and therefore warrants
protection under the Act. The threats to the species of pathogens,
pesticides, and small population size are ongoing and rangewide; they
are likely to continue to act individually and in combination to
decrease the viability of the Franklin's bumble bee. The risk of
extinction is high, the suspected threats to the species persist, and
the number of remaining Franklin's bumble bees is presumably very
small, as the species has not been observed since 2006. Existing
regulatory mechanisms or conservation measures in place do not
appreciably reduce or ameliorate the existing threats to the
[[Page 47222]]
species, as evidenced by the species' acute and rangewide decline.
Therefore, on the basis of the best available scientific and commercial
information, we are listing the Franklin's bumble bee as endangered in
accordance with sections 3(6) and 4(a)(1) of the Act.
Section 4(a)(3) of the Act requires the Secretary of the Interior
(Secretary) to designate critical habitat concurrent with listing to
the maximum extent prudent and determinable. Section 3(5)(A) of the Act
defines critical habitat as (i) the specific areas within the
geographical area occupied by the species, at the time it is listed, on
which are found those physical or biological features (I) essential to
the conservation of the species and (II) which may require special
management considerations or protections; and (ii) specific areas
outside the geographical area occupied by the species at the time it is
listed, upon a determination by the Secretary that such areas are
essential for the conservation of the species. Section 4(b)(2) of the
Act states that the Secretary must make the designation on the basis of
the best scientific data available and after taking into consideration
the economic impact, the impact on national security, and any other
relevant impacts of specifying any particular area as critical habitat.
Because the present or threatened destruction, modification, or
curtailment of habitat is not a threat to the Franklin's bumble bee
(disease and other manmade factors are likely the primary threat to the
species within its habitat), in accordance with 50 CFR 424.12(a)(1), we
determine that designating critical habitat is not prudent for
Franklin's bumble bee.
Peer review and public comment. We sought the expert opinions of 10
appropriate and independent specialists regarding the species status
assessment report. We received responses from 5 specialists, which
informed our determination. We also considered all 53 comments and
information received from the public during the comment period.
Previous Federal Actions
Please refer to the proposed rule (84 FR 40006) for Franklin's
bumble bee published on August 13, 2019, for a detailed description of
previous Federal actions concerning this species.
On August 27, 2019, the Service published a final rule (84 FR
45020) revising the regulations at 50 CFR part 424 for listing species
and designating critical habitat. However, the revisions apply only to
relevant rulemakings for which the proposed rule is published after
September 26, 2019, the effective date of the final rule. Thus, the
prior version of the regulations at 50 CFR part 424 continues to apply
to any rulemakings for which a proposed rule was published before
September 26, 2019, including this final rule for Franklin's bumble
bee.
Summary of Changes From the Proposed Rule
We considered all comments and information we received during the
comment period for the proposed rule to list the Franklin's bumble bee
(84 FR 40006; August 13, 2019). Based on these comments and additional
internal review, we made the following changes from the proposed rule
in this final rule:
Added to this rule and the SSA report additional climate
change information and analysis, as well as discussion on the likely
effects of other potential threats in the future;
Updated this rule and the SSA report with information from
the 2019 survey season;
Corrected a mathematical error in our presentation of
neonicotinoid pesticide applications in the historical range of the
species in this rule and in the SSA report;
Added information from the SSA report to this rule
regarding nectaring behavior, as well as the commercialization of
bumble bees for pollination;
Updated information in this rule on pesticide regulation
on National Wildlife Refuge System lands;
Added further detail in the rule on Tribal notifications;
Added several citations and clarifications to the rule to
further support content; and
Made minor editorial changes to the rule to improve
readability.
We carefully considered the additional information we received
during the comment period, and while much of this information was
helpful, it did not result in any further changes from our proposal to
this final rule to list Franklin's bumble bee as endangered, nor did it
result in a change to our determination that designation of critical
habitat is not prudent at this time.
Supporting Documents
A species status assessment (SSA) team prepared an SSA report for
Franklin's bumble bee. The SSA team was composed of Service biologists,
in consultation with other species experts. The SSA report represents a
compilation of the best scientific and commercial data available
concerning the status of the species, including the impacts of past,
present, and future factors (both negative and beneficial) affecting
the species.
In accordance with our joint policy on peer review published in the
Federal Register on July 1, 1994 (59 FR 34270), we sought the expert
opinions of 10 appropriate and independent specialists regarding the
scientific basis for this proposed rule, detailed in the Franklin's
Bumble Bee Species Status Assessment report (SSA report) (Service
2018a, entire). We received five reviews. The purpose of peer review is
to ensure that our listing and critical habitat determinations are
based on scientifically sound data, assumptions, and analyses. The peer
reviewers have expertise in Franklin's bumble bee or Bombus biology and
habitat, and their comments helped inform our determinations. We also
invited comment on the SSA report from our partner agencies; the U.S.
Forest Service, the Bureau of Land Management, and the Oregon
Department of Agriculture provided us with comments. The comments from
peer and partner reviews were carefully considered in the process of
finalizing the SSA report that provided the scientific basis for both
the proposed rule and this final rule. These comments, along with other
public comments on our proposed rule, are available in the docket for
this final rule (https://www.regulations.gov in Docket No. FWS-R1-ES-
2018-0044).
I. Final Listing Determination
Background
A thorough review of the taxonomy, life history, and ecology of
Franklin's bumble bee is presented in the SSA report (Service 2018a,
entire) on https://www.regulations.gov under Docket No. FWS-R1-ES-2018-
0044. Franklin's bumble bee is thought to have the most limited
distribution of all known North American bumble bee species (Plowright
and Stephen 1980, p. 479; Xerces Society and Thorp 2010, p. 6), and one
of the most limited geographic distributions of any bumble bee in the
world (Frison 1922, p. 315; Williams 1998, p. 129). The species has
been recorded from the Umpqua and Rogue River Valleys in Oregon
(Stephen 1957, p. 81) and from northern California, suggesting its
restriction to the Klamath Mountain region of southern Oregon and
northern California (Thorp et al. 1983, p. 8). Elevations where it has
been observed range from 162 meters (m) (540 feet (ft)) in the northern
part of its range, to over 2,340 m (7,800 ft) in the southern part of
its range. All confirmed specimens have been found in an area about 306
kilometers (km) (190 miles
[[Page 47223]]
(mi)) to the north and south, and 113 km (70 mi) east to west, between
122[deg] to 124[deg] west longitude and 40[deg] 58' to 43[deg] 30'
north latitude in Douglas, Jackson, and Josephine Counties in southern
Oregon, and Siskiyou and Trinity Counties in northern California (Thorp
1999, p. 3; Thorp 2005, p. 1; International Union for Conservation of
Nature 2009, p. 1).
Franklin's bumble bee was first observed in 1917, and first
described in 1921, and limited occurrence and observation data exist
for Franklin's bumble bee prior to 1998. The species has been found on
many privately owned sites as well as municipal, State, and Federal
land. Historical observations and occurrence data for Franklin's bumble
bee prior to 1998 include opportunistic observations, student
collections, and museum specimens, as well as the collections and notes
of interested parties, natural resource managers, and university staff
(Xerces Society and Thorp 2010, pp. 34-40). A more intensive and
targeted search effort for the species began in 1998, in areas thought
to have the highest likelihood of Franklin's bumble bee presence. There
was initial success at finding a higher abundance of the species than
ever previously reported; in one year (1998), 98 Franklin's bumble bees
were observed (mostly from two sites). However, in subsequent years,
searchers found fewer and fewer Franklin's bumble bees, and none have
been found since the last sighting of a single individual in Oregon in
2006. The variations in timing, scope, intensity, and methodology of
search efforts (including those since 1998) and the lack of
observations since 2006 prevent the identification of any population
trends. Many of the occurrence records provide only point data for an
occurrence, with no details on the size of the area searched or whether
or not the record reflected a comprehensive search of an area. Many
records also lack details on the level of survey effort per location
(number of searchers, hours of search effort per day, number of days
per search effort).
The lack of systematic surveys across the historical range of the
species over time prevents us from using occurrence records to
extrapolate reasonable estimates of species abundance or distribution
or from concluding that the species is extinct. Even though none have
been seen since 2006, Franklin's bumble bee populations could
potentially persist undetected. The areas chosen for survey were
selected due to a combination of abundance of floral resources
throughout the colony cycle, relatively recent historical occurrence of
the species, and accessibility to surveyors. However, the surveyed area
represents a relatively small percentage of the historical range of the
Franklin's bumble bee; therefore, it is possible the species may
persist in other areas of the range. There are numerous instances of
species rediscovered after many years, even decades, of having been
believed extinct (e.g., Scheffers et al. 2011, entire). As one example
of such a case, the Fender's blue butterfly (Icaricia icarioides
fenderi) of Oregon was believed extinct after the last recorded
observation in 1937, until it was rediscovered in 1989, 52 years later
(Hammond and Wilson 1992, p. 175; Hammond and Wilson 1993, p. 2).
Recent approaches to evaluating extinction likelihood place increased
emphasis on the extensiveness and adequacy of survey effort (Keith et
al. 2017, p. 321; Thompson et al. 2017, p. 328), and caution against
declaring a species as extinct in the face of uncertainty
(Ak[ccedil]akaya et al. 2017, p. 340).
The specific life-history characteristics and behavior of this rare
species have not been studied; much of the information presented in the
SSA report (Service 2018a, entire) is inferred from information on
Bombus in general and some closely related species (western bumble bee
(B. occidentalis), rusty patched bumble bee (B. affinis), and yellow-
faced bumble bee (B. vosnesenskii), among others). The report also
relied heavily on information from species experts (Service 2018a,
entire).
Franklin's bumble bee is a primitively eusocial bumble bee, meaning
they are highly social and adults have flexible roles in their social
order. They live in colonies made up of a queen and her male and worker
offspring, and adult females can switch from worker to queen roles.
Like other eusocial Bombus species, Franklin's bumble bee typically
nests underground in abandoned rodent burrows or other cavities that
offer resting and sheltering places, food storage, nesting, and room
for the colony to grow (Plath 1927, pp. 122-128; Hobbs 1968, p. 157;
Thorp et al. 1983, p. 1; Thorp 1999, p. 5). The species may also
occasionally nest on the ground (Thorp et al. 1983, p. 1) or in rock
piles (Plowright and Stephen 1980, p. 475). It has even been found
nesting in a residential garage in the city limits of Medford, Oregon
(Thorp 2017, pers. comm.).
Colonies of Franklin's bumble bee have an annual cycle, initiated
each spring when solitary queens emerge from hibernation and seek
suitable nest sites (Thorp 2017, pers. comm.). Colonies may contain
from 50 to 400 workers along with the founding queen (Plath 1927, pp.
123-124; Thorp et al. 1983, p. 2; Macfarlane et al. 1994, p. 7). Two
colonies of Franklin's bumble bee that were initiated in the laboratory
and set out to complete development in the field contained over 60
workers by early September, and likely produced over 100 workers by the
end of the season (Plowright and Stephen 1980, p. 477). The flight
season of Franklin's bumble bee is from mid-May to the end of September
(Thorp et al. 1983, p. 30); a few individuals have been encountered in
October (Southern Oregon University Bee Collection records, in Xerces
Society and Thorp 2010, Appendix 1, p. 39). At the end of the colony
cycle, all the workers and the males die along with the founding queen;
only the inseminated hibernating females (gynes) are left to carry on
the genetic lineage into the following year (Duchateau and Velthius
1988).
As with all Bombus species, Franklin's bumble bee has a unique
genetic system called the haplodiploid sex determination system. In
this system, unfertilized (haploid) eggs become males that carry a
single set of chromosomes, and fertilized (diploid) eggs become females
that carry two sets of chromosomes. This system may result in lower
levels of genetic diversity than the more common diploid-diploid sex
determination system, in which both males and females carry two sets of
chromosomes. Haplodiploid organisms may be more prone to population
extinction than diploid-diploid organisms, due to their susceptibility
to low population levels and loss of genetic diversity (Service 2018a,
p. 37). Inbreeding depression in bumble bees can lead to the production
of sterile diploid males (Goulson et al. 2008, p. 11.7) and negatively
affects bumble bee colony size (Herrman et al. 2007, p. 1167), which
are key factors in a colony's reproductive success.
As one of the rarest Bombus species, Franklin's bumble bees are
somewhat enigmatic, and a specific habitat study for the species has
not been completed. Such a study was initiated in 2006, when the
Franklin's bumble bee was last seen, but could not continue due to the
subsequent absence of the species (Thorp 2017, pers. comm.). However,
some general habitat associations of Bombus are known. Like all bumble
bees, the Franklin's bumble bee requires a constant and diverse supply
of flowers that bloom throughout the colony's life cycle, from spring
to autumn (Xerces Society and Thorp 2010, p. 11); these resources would
typically be found in open (non-forested) meadows in proximity to seeps
and other wet
[[Page 47224]]
meadow environments. The nectar from flowers provides carbohydrates,
and the pollen provides protein. Franklin's bumble bee may have a
foraging distance of up to 10 km (6.2 mi) (Thorp 2017, pers. comm.),
but the species' typical dispersal distance is most likely 3 km (1.86
mi) or less (Hatfield 2017, pers. comm.; Goulson 2010, p. 96).
Franklin's bumble bee have been observed collecting pollen from lupine
(Lupinus spp.) and California poppy (Eschscholzia californica), and
collecting nectar from horsemint or nettle-leaf giant hyssop (Agastache
urticifolia) and mountain monardella (Monardella odoratissima) (Xerces
Society and Thorp 2010, p. 11). Franklin's bumble bee may also collect
both pollen and nectar from vetch (Vicia spp.), as well as rob nectar
from it (Xerces Society and Thorp 2010, p. 11). Short-tongued species,
including Franklin's bumble bee, sometimes visit flowers that are quite
elongated and have difficulty reaching nectar deep in the flower. These
bees can `rob nectar' by chewing a hole on the outside of the flower at
the base, through which they can easily reach the nectar with their
tongues.
In summary, Franklin's bumble bee has been found in a wide array of
sheltered and exposed habitat types at a broad elevational range, and
the species appears to be a generalist forager. Despite uncertainties
regarding the species' habitat needs, we know they need (1) floral
resources for nectaring throughout the colony cycle, and (2) relatively
protected areas for breeding and shelter. The habitat elements that
Franklin's bumble bee appears to prefer to fulfill those needs
mentioned above are relatively plentiful and widely distributed.
Regulatory and Analytical Framework
Regulatory Framework
Section 4 of the Act (16 U.S.C. 1533) and its implementing
regulations (50 CFR part 424) set forth the procedures for determining
whether a species is an ``endangered species'' or a ``threatened
species.'' The Act defines an endangered species as a species that is
``in danger of extinction throughout all or a significant portion of
its range,'' and a threatened species as a species that is ``likely to
become an endangered species within the foreseeable future throughout
all or a significant portion of its range.'' The Act requires that we
determine whether any species is an ``endangered species'' or a
``threatened species'' because of any of the following factors:
(A) The present or threatened destruction, modification, or
curtailment of its habitat or range;
(B) Overutilization for commercial, recreational, scientific, or
educational purposes;
(C) Disease or predation;
(D) The inadequacy of existing regulatory mechanisms; or
(E) Other natural or manmade factors affecting its continued
existence.
These factors represent broad categories of natural or human-caused
actions or conditions that could have an effect on a species' continued
existence. In evaluating these actions and conditions, we look for
those that may have a negative effect on individuals of the species, as
well as other actions or conditions that may ameliorate any negative
effects or may have positive effects.
We use the term ``threat'' to refer in general to actions or
conditions that are known to or are reasonably likely to negatively
affect individuals of a species. The term ``threat'' includes actions
or conditions that have a direct impact on individuals (direct
impacts), as well as those that affect individuals through alteration
of their habitat or required resources (stressors). The term ``threat''
may encompass--either together or separately--the source of the action
or condition or the action or condition itself.
However, the mere identification of any threat(s) does not
necessarily mean that the species meets the statutory definition of an
``endangered species'' or a ``threatened species.'' In determining
whether a species meets either definition, we must evaluate all
identified threats by considering the expected response by the species,
and the effects of the threats--in light of those actions and
conditions that will ameliorate the threats--on an individual,
population, and species level. We evaluate each threat and its expected
effects on the species, then analyze the cumulative effect of all of
the threats on the species as a whole. We also consider the cumulative
effect of the threats in light of those actions and conditions that
will have positive effects on the species, such as any existing
regulatory mechanisms or conservation efforts. The Secretary determines
whether the species meets the definition of an ``endangered species''
or a ``threatened species'' only after conducting this cumulative
analysis and describing the expected effect on the species now and in
the foreseeable future.
Analytical Framework
The SSA report documents the results of our comprehensive
biological review of the best available scientific and commercial data
regarding the status of the species, including an assessment of the
potential threats to the species. The SSA report does not represent a
decision by the Service on whether the species should be listed as an
endangered or threatened species under the Act. It does, however,
provide the scientific basis that informs our regulatory decisions,
which involve the further application of standards within the Act and
its implementing regulations and policies. The following is a summary
of the key results and conclusions from the SSA report; the full SSA
report can be found at Docket No. FWS-R1-ES-2018-0044 on https://www.regulations.gov.
To assess the viability of Franklin's bumble bee, we used the three
conservation biology principles of resiliency, redundancy, and
representation (Shaffer and Stein 2000, pp. 306-310). Briefly,
resiliency supports the ability of the species to withstand
environmental and demographic stochasticity (for example, wet or dry,
warm or cold years), redundancy supports the ability of the species to
withstand catastrophic events (for example, droughts, large pollution
events), and representation supports the ability of the species to
adapt over time to long-term changes in the environment (for example,
climate changes). In general, the more resilient and redundant a
species is and the more representation it has, the more likely it is to
sustain populations over time, even under changing environmental
conditions. Using these principles, we identified the species'
ecological requirements for survival and reproduction at the
individual, population, and species levels, and described the
beneficial and risk factors influencing the species' viability.
The SSA process can be categorized into three sequential stages.
During the first stage, we evaluated the individual species' life-
history needs. The next stage involved an assessment of the historical
and current condition of the species' demographics and habitat
characteristics, including an explanation of how the species arrived at
its current condition. The final stage of the SSA involved making
predictions about the species' responses to positive and negative
environmental and anthropogenic influences. Throughout all of these
stages, we used the best available information to characterize
viability as the ability of a species to
[[Page 47225]]
sustain populations in the wild over time. We use this information to
inform our regulatory decision.
Summary of Biological Status and Threats
In this discussion, we review the biological condition of the
species and its resources, and the threats that influence the species'
current and future condition, in order to assess the species' overall
viability and the risks to that viability.
To assess resiliency and redundancy, we evaluated the change in
Franklin's bumble bee occurrences (populations) over time. To assess
representation (as an indicator of adaptive capacity) of the Franklin's
bumble bee, we evaluated the spatial extent of occurrences over time.
We evaluated the change in resiliency, representation, and redundancy
from the past until the present; however, due to the lack of
observations of the species since 2006, we did not project anticipated
future states of these conditions.
Our analyses indicate that the resiliency, redundancy, and
representation of the Franklin's bumble bee have all declined since the
late 1990s. Historically, the species has always been rare and has one
of the narrowest distributions of any Bombus species in the world. Even
so, the abundance and distribution of Franklin's bumble bee has
declined significantly (Service 2018a, pp. 10-14); the species has not
been observed since 2006, despite intensive survey efforts in select
portions of its historical range. Search efforts for the species have
been varied in timing, scope, intensity, and methodology. During the
more intensive surveys from 1998 until the last observation in 2006,
the Franklin's bumble bee was observed at 14 locations, including 8
locations where it had not been previously documented. In 1998, 98 bees
were found among 11 locations. Searchers found fewer and fewer bees
after that year even though they continued extensive searches in
multiple locations with the highest likelihood of finding the species.
Twenty bees were located in 1999, nine individuals were observed in
2000, and one individual was observed in 2001. Although 20 Franklin's
bumble bees were observed in 2002, only 3 were observed in 2003 (all at
a single locality), and a single worker bee was observed in 2006.
Despite continued intensive search efforts in these areas through 2019,
there have been no confirmed observations of the Franklin's bumble bee
since 2006. Data allow us to estimate 43 potential populations of the
species since 1921, when the first description of the species was
published (Service 2018a, pp. 11). From 1998 to 2006, we identified 14
potential populations. Since 2006, no populations have been located.
The vulnerability resulting from the Franklin's bumble bee's
haplodiploid genetic system, as well as the loss in the abundance and
spatial extent of its populations, suggest the resiliency,
representation, and redundancy of the Franklin's bumble bee have all
declined significantly since the late 1990s. The losses in both the
number of populations and their spatial extent render the Franklin's
bumble bee vulnerable to extinction even without further external
stressors (e.g., pathogens and insecticide exposure) acting upon the
species.
As part of our status assessment of the Franklin's bumble bee, we
looked at potential stressors affecting the species' viability (Service
2018a, pp. 23-40). Potential stressors that we analyzed for the
Franklin's bumble bee generally fit into three groups that correspond
with Factors A (habitat loss and fragmentation), C (pathogens), or E
(pesticide use, competition with nonnative bees, and effects of small
population size). No potential stressors of the Franklin's bumble bee
correspond with Factor B. There has never been any indication that the
Franklin's bumble bee was at risk of overutilization for commercial,
recreational, scientific, or educational purposes, and we did not find
any new information to suggest this has changed. Existing regulatory
mechanisms (Factor D) are discussed below in the context of how they
help to reduce or ameliorate stressors to the Franklin's bumble bee.
The 2010 petition identified destruction, degradation, and
conversion of habitat as a threat to the Franklin's bumble bee. In our
90-day finding on the 2010 petition (76 FR 56381; September 13, 2011),
we noted that the petitioners provided substantial information on
threats to the Franklin's bumble bee from the destruction,
modification, or curtailment of habitat, primarily due to the potential
impacts of natural or prescribed fire. Because the loss and degradation
of habitat has been shown to reduce both diversity and abundance in
other Bombus species (Potts et al. 2010, pp. 348-349), we looked at the
potential stressors of natural or prescribed fire, agricultural
intensification, urban development, livestock grazing, and the effects
of climate change (Service 2018a, pp. 23-40).
Although conversion of natural habitat appears to be the primary
cause of bumble bee habitat loss throughout the world (Goulson et al.
2015, p. 2; Kosior et al. 2010, p. 81), many researchers believe it is
unlikely to be a main driver of the recent, widespread North American
bee declines (Szabo et al. 2012, p. 236; Colla and Packer 2008, p.
1388; Cameron et al. 2011, p. 665). Despite uncertainties regarding the
Franklin's bumble bee's habitat needs, we know they need (1) floral
resources for nectaring throughout the colony cycle, and (2) relatively
protected areas for breeding and shelter. Furthermore, the available
information regarding locations where the species has been found
indicates that the Franklin's bumble bee is a generalist forager and
that the species' specific needs and preferences for these habitat
elements are relatively flexible, plentiful, and widely distributed.
While we can say that Bombus species in general might prefer protected
meadows with an abundance of wildflowers, the Franklin's bumble bee has
been found in a wide array of sheltered and exposed habitat types at
elevations ranging from 540 ft (162 m) to 7,800 ft (2,340 m) (Thorp
2017, pers. comm.).
Natural or Prescribed Fire
Fire caused by both natural and human-caused factors has been an
important change on the landscape in the range of the Franklin's bumble
bee. Because fire reduces natural succession of forests through the
burning of encroaching woody plants, fire is a primary factor in the
maintenance of grassland and meadow habitat that can support Bombus
species (Shultz and Crone 1998, p. 244; Huntzinger 2003, p. 2). With
the increase in human development came fire suppression to limit damage
to manmade structures. Fire suppression allows woody encroachment to
occur, and the diverse landscape created by fire (open areas mixed
within forested areas) is slowly being replaced by increasing areas of
denser forested habitat; the open areas that facilitated the growth of
diverse understory plant communities are being reduced from their
historical condition (Ruchty 2011, p. 26). Conifer species now cover
some of the area that was previously open meadow habitat in the range
of the Franklin's bumble bee (Panzer 2002, p. 1297; Shultz and Crone
1998, p. 244). Although this loss of habitat by fire suppression may
have limited the availability and diversity of floral resources, as
well as nest and overwintering habitat for the Franklin's bumble bee,
healthy meadow habitat remains in areas where the Franklin's bumble bee
was previously found (Godwin 2017, pers comm.; Colyer 2017, pers.
comm.), and it is unlikely
[[Page 47226]]
that loss of habitat from fire suppression was a factor in the decline
of the species.
Increased fuel loads from fire suppression heighten the potential
for catastrophic, large-scale, and high temperature wildfires. Any
Bombus colonies in the path of this type of fire would be at risk of
extirpation. Wildfire may have extirpated some historical populations
of the Franklin's bumble bee, but we have no information suggesting
that any known Franklin's bumble bee occurrence sites were in the path
of catastrophic wildfires at the time the sites were occupied.
Controlled burning became a management tool for reducing potential fuel
loads for wildfire; controlled burning is carried out by Federal land
management agencies including the U.S. Forest Service and Bureau of
Land Management in the range of the Franklin's bumble bee. The effects
of fire on invertebrates depends greatly on the biology of the specific
taxa (Gibson et al. 1992, p. 166), and in the case of the Franklin's
bumble bee, controlled burns could certainly cause death of individual
bees and negative effects to a colony. Prescribed fire is likely to
continue to be used as a management tool on some Federal land; however,
the practice is overall small in scale, opportunistic (depending on
weather, funding, and a host of other factors), used to prevent
catastrophic fire, and often a net benefit to pollinators as it opens
habitat by decreasing canopy cover (U.S. Forest Service 1989, IV 87 to
IV 90, IV-113 to IV-119; U.S. Forest Service 1990, pp 4-149 to 4-179).
In summary, we have no information to indicate that controlled burns
were a factor in the decline of the Franklin's bumble bee or will
increase in the future to a degree that may affect the viability of the
species.
Agricultural Intensification
Agricultural intensification can result in habitat loss for bumble
bees, as these practices often result in the planting of monocultures
that tend to provide floral resources for a limited period of time,
rather than throughout the colony's life cycle. Agricultural
intensification can negatively impact wild bees by reducing floral
resource diversity and abundance (Service 2018a, p. 32). Agricultural
intensification was determined to be a primary factor leading to the
local extirpation and decline of bumble bees in Illinois (Grixti et al.
2009, p. 75). An increased use of herbicides often accompanies
development and agricultural intensification, and the widespread use of
herbicides in agricultural, urban, and even natural landscapes has led
to decreases in flowering plants (Potts et al. 2010, p. 350).
Within the historical range of the Franklin's bumble bee, total
acres in agricultural cropland decreased in all three counties in
Oregon (Douglas, Jackson, and Josephine) by greater than 50 percent
from 1997 to 2012 (U.S. Department of Agriculture--National Agriculture
Statistics Service 2017, pers. comm.; Service 2018a, p. 33). While the
total number of acres of agricultural cropland is not synonymous with
agricultural intensification (specifically, the expansion of
monocultures), a decrease in total acres of agriculture leads us to
conclude that agricultural intensification was not likely a factor in
the decline of the Franklin's bumble bee. We have no documentation in
our files or any direct evidence that agricultural intensification has
contributed to the decline of the Franklin's bumble bee or will
increase in the future to a degree that may affect the viability of the
species. Approximately 42 percent of sites where Franklin's bumble bees
have ever been reported (18 of 43) occur on federally owned land,
primarily U.S. Forest Service and Bureau of Land Management land; very
little habitat on these lands has been permanently altered or lost
through agricultural intensification (Service 2018a, p. 32).
Urban Development
Ongoing urbanization contributes to the loss and fragmentation of
natural habitats. Urban gardens and parks provide habitat for some
pollinators, including bumble bees (Frankie et al. 2005, p. 235;
McFrederick and LeBuhn 2006, p. 372), but they tend not to support the
species richness of bumble bees that can be found in nearby undeveloped
landscapes (Xerces Society and Thorp 2010, p. 13) or that which was
present historically (McFrederick and LeBuhn 2006). However, Franklin's
bumble bee and western bumble bee have both been observed in urban
areas of Ashland, Oregon, and in residential areas of Medford, Oregon.
Furthermore, approximately 42 percent of the sites where Franklin's
bumble bee have ever been reported (18 of 43) occur on federally owned
land, primarily U.S. Forest Service and Bureau of Land Management land,
and very little habitat on these lands has been permanently altered or
lost through development.
Generally good habitat conditions currently exist throughout the
known historical Franklin's bumble bee locations and all of the recent
focused survey areas. Two notable events occurred in areas with
previous observations of Franklin's bumble bee: The creation of Lake
Applegate upon the completion of Applegate Dam in the fall of 1980, and
a report of soil modification on a portion of the Gold Hill site in
2004; however, we have no information to indicate that Franklin's
bumble bees were still in the vicinity or had any colonies in the area
when these events occurred. The Applegate Dam project inundated two
sites with historical observations of Franklin's bumble bee (from the
1960s), but no subsequent search efforts or observations (Xerces
Society and Thorp 2010, p. 13; Thorp, pers. comm. 2017). The June 23,
2010, petition noted that in 2004, soil had been excavated and
deposited in a portion of the Gold Hill area (Xerces Society and Thorp
2010, p. 13). The last observation of Franklin's bumble bee at Gold
Hill was in the year 2000, and the site was revisited 14 times over the
next 3 years with no observations of Franklin's bumble bee. In both of
these cases, we have no information to suggest the species was still
using the habitat in the area by the time the activities took place,
and therefore no information to suggest that either of these events
affected the resiliency of any population of Franklin's bumble bee. We
have no documentation in our files or any direct evidence that
urbanization or development in the range of Franklin's bumble bee, or
the incidents described above, contributed to the decline of the
species or will increase in the future to a degree that may affect the
viability of the species (Portland State University 2015, p. 7).
Livestock Grazing
Livestock grazing occurs on public land in much of the historical
range of the Franklin's bumble bee. Overgrazing by sheep between 1890
and 1920 resulted in trampling vegetation and denuding soils, and
grazing is currently evident today in the continuing erosion of the
granitic soils of the McDonald Basin, Siskiyou Gap, Mt. Ashland, and
the Siskiyou Crest (LaLande 1995, p. 31; T. Atzet 2017, pers. comm.).
Several studies on the impacts of livestock grazing on bees suggest
that an increase in the intensity of livestock grazing affects the
species richness of bees (Service 2018a, p. 35). In contrast, grazing,
especially by cattle, can play a key positive role in maintaining the
abundance and species richness of preferred bumble bee forage (Carvell
2002, p. 44). Evidence of livestock grazing was observed interspersed
within abundant floral resources in Franklin's bumble bee habitat
during several recent targeted survey efforts
[[Page 47227]]
(Brooks 1997, pers. comm.; Service 2016, entire; Service 2017, entire;
Trail 2017, pers. comm.). We have no new information that the timing,
location, intensity, or duration of grazing has changed, with the
exception of the Cascade-Siskiyou National Monument, where most grazing
has been retired (Colyer 2018, pers. comm.). The lack of specific
information on the impacts of livestock grazing on the Franklin's
bumble bee limits our ability to connect the activity to any specific
species' response, and we do not anticipate grazing will increase in
the future to a degree that may affect the viability of the species
(Bureau of Land Management 2016, pp. 96-103).
Effects of Climate Change
Specific impacts of climate change on pollinators are not well
understood; most of the existing information on climate change impacts
to pollinators comes from studies on butterflies. Studies specifically
relating to bumble bees are scant, and we found no climate change
information specific to the Franklin's bumble bee. Changes in
temperature and precipitation, and the increased frequency of storm
events, can affect pollinator population sizes directly, by affecting
survival and reproduction (Intergovernmental Panel on Climate Change
2013, entire; Bale et al. 2002, p. 11; Roland and Matter 2016, p. 22).
These climatic changes can also affect populations indirectly, by
altering resource availability and species interactions (Service 2018a,
p. 36).
Bumble bee abundance for three species of Bombus in the Rocky
Mountains increased when floral resources were available for more days,
and the number of days when floral resources were available increased
with greater summer precipitation and later snowmelt dates (Ogilvie et
al. 2017, p. 4). Several of the targeted Franklin's bumble bee and
western bumble bee survey reports between 2015 and 2017 include mention
of widespread hot, dry climate affecting timing and abundance of floral
resources during the surveys (Bureau of Land Management 2015, p. 2;
Trail 2017, pers. comm.). Although the Olgilvie et al. study and the
survey reports suggest potential indirect effects of climate change on
Bombus, we have no information to indicate that the effects of climate
change were connected to the decline of the Franklin's bumble bee;
numerous Bombus species persist in areas that are considered good
quality habitat for the Franklin's bumble bee (Pool 2014, entire;
Colyer 2016, entire). As a habitat generalist, Franklin's bumble bee
appears to forage on a variety of floral resources, and we have no
information to suggest that they would not forage off of whatever
floral resource was in bloom at the time they emerge from their nests.
We have no information to suggest that any changes in the vegetation
community to date led to the decline of the species.
In order to understand the potential future impact of climate
change on Franklin's bumble bee, we looked at climate change projection
models. Global climate projections are informative and, in some cases,
the only or the best scientific information available for us to use.
However, projected changes in climate and related impacts can vary
substantially across and within different regions of the world
(Intergovernmental Panel on Climate Change 2007, pp. 8-12). Therefore,
we use ``downscaled'' projections when they are available and have been
developed through appropriate scientific procedures because such
projections provide higher-resolution information that is more relevant
to spatial scales used for analyses of a given species (see Glick et
al. 2011, pp. 58-61, for a discussion of downscaling).
Downscaled projections as of 2016 were available for our analysis
of the Franklin's bumble bee from the U.S. Geological Survey's National
Climate Change Viewer (Alder, J. and S. Hostetler. 2016, entire). The
National Climate Change Viewer is based on the mean of 30 models, which
can be used to predict changes in air temperature and precipitation for
Jackson County, Oregon (location of the last known occurrence record of
Franklin's bumble bee), for two greenhouse gas emission scenarios,
RCP4.5 and RCP8.5. From the year 2020 to the year 2050, the model set
shows an increase in the mean maximum air temperature of between 1.9
degrees Fahrenheit ([deg]F) (1 degree Celsius ([deg]C)) (RCP4.5) and
3.1 [deg]F (1.7 [deg]C) (RCP8.5), and an increase in the mean annual
minimum air temperature of between 1.0 [deg]F (0.3 [deg]C) (RCP4.5) and
2.7 [deg]F (1.5 [deg]C) (RCP8.5). For both scenarios, mean
precipitation is predicted to decrease by approximately 0.4 inches (10
millimeters) for both scenarios.
Projections for an increase in temperature and decrease in
precipitation over the next 30 years may lead to alteration in the
vegetation community in Franklin's bumble bee habitat, including the
varieties of floral resources that Franklin's bumble bee relies on for
nectar. However, we have no information to suggest that these changes
will result in a decrease in the availability of nectar resources to
the species. Some studies suggest that pollinators are responding to
climate change with recent latitudinal and elevational range shifts
such that there is spatial mismatch among plants and their pollinators;
while this has been demonstrated in butterflies, it may be less of a
factor for bumble bees (Service 2018a, p. 36). As generalist foragers,
bumble bees do not require synchrony with a particular plant species,
although some bumble bee populations are active earlier in the season
than in the past (Bartomeus et al. 2011, p. 20646).
Projections for an increase in temperature and decrease in
precipitation over the next 30 years may also affect the frequency or
intensity of wildfires and storm events (including flooding). These
events could affect the availability of floral resources, the
suitability of nest locations, and the survival of overwintering
queens. However, we do not have information projecting the timing,
scope, or intensity of wildfires or storms; the stochastic nature of
these events limits our ability to project the magnitude of impact on
the future condition of Franklin's bumble bee or its habitat, and
hinders our ability to assess their impact on the viability of the
species.
Summary
Although habitat loss has had negative effects on bumble bees, we
conclude it is unlikely to be a main driver of the decline of the
Franklin's bumble bee. Habitat appears generally intact and in good
condition throughout the known, historical locations of the Franklin's
bumble bee and throughout all of the recent focused survey areas (with
the exceptions of the historical sites affected by the creation of Lake
Applegate in the fall of 1980, and soil modification that occurred on a
portion of the Gold Hill site in 2004). In our assessment, we found no
information to suggest that destruction, degradation, or conversion of
habitat occurred at a scope and magnitude that would cause it to be a
primary factor in the decline of the Franklin's bumble bee (Service
2018a, pp. 35-37). Furthermore, we have no information to suggest that
habitat destruction or modification will increase in scope and
magnitude to the point where it will be a primary stressor to the
species in its range in the near future.
A number of diseases and parasites are known to occur in bumble bee
populations. These include the protozoan parasite Crithidia bombi (C.
bombi), the tracheal mite Locustacarus buchneri, the microsporidium
(parasitic fungus) Nosema bombi (N. bombi), as well as deformed wing
virus. Pathogens
[[Page 47228]]
and parasites are widespread generalists in the host genus, but affect
species differently according to host susceptibility and tolerance to
infection (Kissinger et al. 2011, p. 221; Malfi and Roulston 2014, p.
18). The host species' life history plays a role in the virulence of a
given pathogen; for instance, parasites may have relatively smaller
effects on species with shorter colony life cycles and smaller colony
sizes (Rutrecht and Brown 2009, entire).
Pathogen spillover is a process whereby parasites and pathogens
spread from commercial bee colonies to native bee populations (Colla et
al. 2006, p. 461; Otterstatter and Thompson 2008, p. 1). The decline of
certain Bombus species from the mid-1990s to present, particularly
species in the subgenus Bombus sensu stricto (including Franklin's
bumble bee), was contemporaneous with the collapse of commercially bred
western bumble bee (raised primarily to pollinate greenhouse tomato and
sweet pepper crops beginning in the late 1980s) (Szabo et al. 2012, pp.
232-233). This collapse was attributed to infections of Nosema bombi.
Nosema bombi has been detected in native bumble bees in North
America, and has been found to be a part of the natural pathogen load.
The fungus has been reported in Canada since the 1940s (Cordes et al.
2011, p. 7) and appears to have a broad host range in North American
(Kissinger et al. 2011, p. 222). Infections of the pathogen primarily
occur in the malpighian tubules (small excretory or water regulating
glands), but also in fat bodies, nerve cells, and sometimes the trachea
(Macfarlane et al. 1995). Bombus colonies can appear to be healthy but
still carry N. bombi and transmit it to other colonies, most likely
when spores are fed to larvae and then infected adults drift into non-
natal colonies (Service 2018a, p. 25).
While we have no evidence of direct effects of a virulent strain of
N. bombi on the Franklin's bumble bee, N. bombi has been detected in
closely related species in the range of the Franklin's bumble bee.
Furthermore, N. bombi infections in rare species like the Franklin's
bumble bee are more frequent, are more severe, and seem to affect a
higher percentage of individuals of the species (Cameron et al. 2011,
entire; Cordes et al. 2011, p. 2).
The effect of pathogens on bumble bees varies from mild to severe
(Macfarlane et al. 1995; Rutrecht et al. 2007, p. 1719; Otti and
Schmid-Hempel 2008, p. 577). Bumble bees infected with Nosema bombi may
have crippled wings, and queens may have distended abdomens and be
unable to mate (Otti and Schmid-Hempel 2007, pp. 122-123). Malfi and
Roulston (2014, p. 24) found that N. bombi infections are more frequent
and more severe in rare species, and the species with the highest
percentages of infected individuals were rare species. Furthermore, the
effects of pathogen infection on bumble bees may be amplified by other
influence factors. Nutritional stress may compromise the ability of
bumble bees to survive parasitic infections, as evidenced by a
significant difference in mortality in bumble bees on a restricted diet
compared to well-fed bees infected with C. bombi (Brown et al. 2000,
pp. 424-425).
A virulent strain of Nosema bombi from the buff-tailed bumble bee
(Bombus terrestris) may have spread to the eastern bumble bee (B.
impatiens) and western bumble bee from Europe. In the mid-1990s,
companies shipped queen eastern and western bumble bees to Europe for
their development into colonies to use in commercial pollination
services. When the colonies had reached sufficient size, they were
shipped back to the United States and deployed in industrial greenhouse
operations in California, primarily to pollinate tomatoes and peppers.
The colonies may have picked up N. bombi prior to their shipment back
into the United States, and once in this country, the commercially
reared colonies may have spread the virulent strain to wild populations
of Franklin's bumble bee (Xerces Society and Thorp 2010, p. 14). In
work partially funded by the Service, the University of Illinois
conducted surveys for parasites and pathogens in bumble bee populations
of the Pacific Northwest and Midwest between 2005 and 2009. The goal
was to assess Bombus populations for presence and prevalence of
pathogens, particularly microsporidia, in an effort to provide baseline
data to assess disease as a potential factor in the decline of the
Franklin's bumble bee, western bumble bee, and American bumble bee (B.
pensylvanicus) (Solter et al. 2010, p. 1). The highest prevalence of N.
bombi was found in western bumble bee, with 26 percent of collected
individuals infected. Crithidia bombi infections of western bumble bee
were 2.8 percent overall (Solter et al. 2010, pp. 3-4); no Franklin's
bumble bees were collected during the study. However, Mt. Ashland,
Oregon, was one of only three sites in the Pacific Northwest study area
where N. bombi infections were found in multiple Bombus species (the
indiscriminate cuckoo bumble bee (B. insularis) and black-notched
bumble bee (B. bifarius)) (Solter et al. 2010, pp. 3-4). Although
Cordes et al. (2011, p. 7) found a new allele in N. bombi, the recent
study by Cameron et al. (2016) found no evidence of an exotic strain of
N. bombi.
In summary, known pathogens occur within the historical range of
the Franklin's bumble bee, and we have evidence of several pathogens
infecting closely related species within that range that have also
likely affected the Franklin's bumble bee. Although we have no direct
evidence of pathogens playing a role in the decline of the Franklin's
bumble bee, the disappearance of the Franklin's bumble bee occurred
soon after a period of potential exposure to introduced pathogens,
particularly N. bombi, which is known to have a more severe impact on
rare species like the Franklin's bumble bee. Decline of other closely
related pollinators has been associated with these pathogens, and it is
highly likely pathogens have had some negative influence on the
resiliency of Franklin's bumble bee populations.
Pesticide Use
Exposure to pesticides can occur to bumble bees from direct spray
or drift, or from gathering or consuming contaminated nectar or pollen
(Johansen and Mayer 1990; Morandin et al. 2005, p. 619). Lethal and
sublethal effects on bumble bee eggs, larvae, and adults have been
documented for many different pesticides under various scenarios
(Service 2018a, p. 28). Documented sub-lethal effects to individual
bumble bees and colonies include reduced or no male production, reduced
or no egg hatch, reduced queen production, reduced queen longevity,
reduced colony weight gain, reduced brood size, reduced feeding,
impaired ovary development, and an increased number of foragers or
foraging trips or duration (interpreted as risky behaviors) (Service
2018a, p. 28). Bumble bee habitat can also be impacted by pesticides
due to changes in vegetation and the removal or reduction of flowers
needed to provide consistent sources of pollen, nectar, and nesting
material (Service 2018a, p. 28). Declines in bumble bees in parts of
Europe have been at least partially attributed to the use of pesticides
(Williams 1986, p. 54; Kosior et al. 2007, p. 81).
Although the use of land for agricultural purposes has
traditionally involved the use of pesticides and other products toxic
to bees, one particular class of insecticides known as neonicotinoids
have been strongly implicated in the decline of honey bees (Apis spp.)
worldwide, and implicated in the decline of several Bombus
[[Page 47229]]
species, including rusty patched bumble bee, buff-tailed bumble bee,
and eastern bumble bee (Pisa et al. 2015, p. 69; Goulson 2013, pp. 7-8;
Colla and Packer 2008, p. 10; Lundin et al. 2015, p. 7). Neonicotinoids
are a broad class of insecticides based on nicotine compounds used in a
variety of agricultural applications; they act as a neurotoxin,
affecting the central nervous system of insects by interfering with the
receptors of the insects' nervous system, causing overstimulation,
paralysis, and death (Douglas and Tooker 2015, pp. 5090-5092). The
neonicotinoid family of insecticides includes acetamiprid,
clothianidin, imidacloprid, nitenpyram, nithiazine, thiacloprid, and
thiamethoxam. In the range of the Franklin's bumble bee (Jackson,
Douglas, and Josephine Counties in Oregon, as well as Trinity and
Siskiyou Counties in California), the first reported use of
imidacloprid was in 1996, thiamethoxam in 2001, and clothianidin in
2004. The use of neonicotinoid pesticides continued in the range of the
species through 2006, when the last observation of the Franklin's
bumble bee was recorded. Across all five counties, total estimated
applications of these three neonicotinoids increased from 53.31 pounds
(lbs) (24.19 kilograms (kg)) in 1996, to 1,144.6 lbs (519.9 kg) in
2014. However, the exponential growth of neonicotinoid applications
started in 2011, 5 years after the last observation of the species. The
vast majority of neonicotinoids are used as seed treatments on grains
and other field crops (Oregon Department of Agriculture 2018, pers.
comm.), and total agricultural land within the historical range of the
species is less than 2 percent of the total land base (2011 National
Land Cover Data Set and 2016 USDA Crop Data Layers (CDL) in Syngenta
2019, pers. comm).
No studies have investigated the effects of pesticide use on the
Franklin's bumble bee, and no discoveries have been documented of any
Franklin's bumble bees injured or killed by pesticides. The Franklin's
bumble bee is a habitat generalist and is not known to have a close
association with agricultural lands; therefore, it may have less
exposure to pesticides than some other Bombus species. However,
pesticide use occurs in the range of the Franklin's bumble bee. The
similarity in foraging traits that the Franklin's bumble bee has with
both honey bees and the other Bombus species (e.g., generalist foragers
collecting pollen from similar food sources) allows us to infer that
Franklin's bumble bee populations are likely to suffer exposure to and
impacts from pesticides in similar measure to other Bombus species when
the Franklin's bumble bee is in areas where pesticides are applied.
Effects of Small Population Size
The Franklin's bumble bee is rare and has always had very small
populations (relative to other similar, native bumble bees in the
western United States), and likely has low genetic diversity due to the
haplodiploid genetic system it shares with all Bombus species (Zayed
2009, p. 238). These factors make the species more vulnerable to
habitat change or loss, parasites, diseases, stochastic events, and
other natural disasters such as droughts (Xerces Society and Thorp
2010, p. 20). Between 1998 and 2006, the number of Franklin's bumble
bee observations went from a high of 98 at 11 locations, to a lone
individual in 2006. No observations of the Franklin's bumble bee have
occurred since 2006, despite an increase in survey effort. Diploid male
production has been detected in naturally occurring populations of
bumble bees, and recent modeling work has shown that diploid male
production may initiate a rapid extinction vortex (a situation in which
genetic and demographic traits and environmental conditions reinforce
each other in a downward spiral, leading to extinction) (Goulsen et al.
2008, p. 11.8). Because of inbreeding and the production of sterile
males, the haplodiploid genetic system makes bumble bees very
vulnerable when populations get small (Colla 2018, pers. comm.).
Although we have no direct evidence that small population size or a
rapid extinction vortex contributed to the decline of the species, the
genetic system and historically small population size of the Franklin's
bumble bee likely heightened the species' vulnerability to other
threats in the environment; we, therefore, consider the effects of
small population size a synergistic threat to the species.
Competition With Nonnative Bees
The European honey bee (Apis mellifera) was first introduced to
eastern North America in the early 1620s, and into California in the
early 1850s (Xerces Society and Thorp 2010, p. 21). The resource needs
of the European honey bee and native Bombus species may overlap,
resulting in the potential for increased competition for resources
(Thomson 2004, p. 458; Thomson 2006, p. 407). Decreased foraging
activity and lowered reproductive success of Bombus colonies have been
noted near European honey bee hives (Evans 2001, pp. 32-33; Thomson
2004, p. 458; Thomson 2006, p. 407). Additionally, the size of workers
of native Bombus species were noticeably reduced where European honey
bees were present, which may be detrimental to Bombus colony success
(Goulson and Sparrow 2009, p. 177). It is likely that the effects
discussed in these studies are local in space and time, and most
pronounced where floral resources are limited and large numbers of
commercial European honey bee colonies are introduced (Xerces Society
and Thorp 2010, p. 21). We have no information to indicate that any
area of Franklin's bumble bee habitat in the range of the species has
limited floral resources and large numbers of European honey bees. We
have no information related to the specific placement of commercial
honey bee colonies in or near Franklin's bumble bee habitat.
Furthermore, European honey bees have been present without noticeable
declines in Bombus populations over large portions of their ranges
(Xerces Society and Thorp 2010, p. 21), and we have no new information
that connects competition from European honey bees to the decline of
the Franklin's bumble bee.
There is potential for nonnative, commercially raised bumble bees
to naturalize and outcompete native bumble bees for limited resources
such as nesting sites and forage areas. Five commercially reared
eastern bumble bee workers and one queen were captured in the wild near
greenhouses where commercial bumble bees are used, suggesting this
species may have naturalized outside of its native range. The eastern
bumble bee, which has a native range in eastern North America, was
detected in western Canada (Ratti and Colla 2010, pp. 29-31). In Japan,
nonnative buff-tailed bumble bee colonies founded by bees that had
escaped from commercially produced colonies had more than four times
the mean reproductive output of native bumble bees (Matsumura et al.
2004, p. 93). In England, commercially raised buff-tailed bumble bee
colonies had higher nectar-foraging rates and greater reproductive
output than a native subspecies of the buff-tailed bumble bee (Ings et
al. 2006, p. 940). Colonies of eastern bumble bee were imported to
pollinate agricultural crops and strawberries in Grants Pass, Oregon,
in the range of the Franklin's bumble bee (Xerces Society and Thorp
2010, p. 18).
Although nonnative Bombus species in the range of Franklin's bumble
bee could outcompete Franklin's bumble bee for floral resources and
nesting habitat, we have no information to definitively connect
competition with
[[Page 47230]]
nonnative bumble bees to the decline of the Franklin's bumble bee.
Furthermore, invertebrate surveys in Franklin's bumble bee habitat
continue to show evidence of healthy populations of other native Bombus
species unaffected by competition from nonnative bees (Pool 2014,
entire; Colyer 2016, entire).
Summary
We find that several natural and other human-caused factors
contributed to the decline of the Franklin's bumble bee. While it is
unlikely that pesticides alone can account for the decline of the
Franklin's bumble bee, documented effects of pesticides on closely
related Bombus species suggest pesticide use was likely a factor in the
decline of the Franklin's bumble bee. The haplodiploid genetic system
of the Franklin's bumble bee, combined with its historically small
population size, was also likely a factor in the decline of the
species. Although nonnative Bombus species in the range of the
Franklin's bumble bee could outcompete the Franklin's bumble bee for
floral resources and nesting habitat, we have no information connecting
competition with nonnative bumble bees to the decline of the Franklin's
bumble bee. Additionally, surveys in Franklin's bumble bee habitat
continue to show evidence of healthy populations of other native Bombus
species unaffected by competition from nonnative bees.
Synergistic and Cumulative Effects
It is likely that several threats are acting cumulatively and
synergistically on many Bombus species, including the Franklin's bumble
bee (Goulson et al. 2015, p. 5), and the combination of multiple
threats is likely more harmful than any one acting alone (Gill et al.
2012, p. 108; Coors and DeMeester 2008, p. 1821; Sih et al. 2004, p.
274). There is recent evidence that the interactive effects of
pesticides and pathogens could be particularly harmful for bumble bees
(Service 2018a, p. 39). Nutritional stress may compromise the ability
of bumble bees to survive parasitic infections (Brown et al. 2000, pp.
424-425). Bumble bees with activated immunity may have metabolic costs,
such as increased food consumption (Tyler et al. 2006, p. 2; Moret and
Schmid-Hempel 2000, pp. 1166-1167). Additionally, exposure to
pesticides may increase with increased food consumption in infected
bees (Goulson et al. 2015, p. 5). Activating immunity impairs learning
in bumble bees (Riddell and Mallon 2006; Alghamdi et al. 2008, p. 480).
Impaired learning is thought to reduce the ability of bees to locate
floral resources and extract nectar and pollen, therefore exacerbating
nutritional stresses (Goulson et al. 2015, p. 5). Further, declining
North American species with low genetic diversity have higher
prevalence of the pathogen Nosema bombi (Cameron et al. 2011, p. 665).
In summary, we, therefore, find that pathogens in combination with
pesticides, as well as pathogens in combination with the effects of
small population size, may have hastened and amplified the decline of
the Franklin's bumble bee to a greater degree than any one of the three
threats would cause on its own.
Existing Regulatory Mechanisms and Conservation Efforts
Surveys conducted by Dr. Robbin Thorp, other private individuals,
university classes and researchers, the U.S. Forest Service, and Bureau
of Land Management have significantly contributed to the existing
information on Franklin's bumble bee. However, other than those search
efforts, we are aware of no conservation efforts or beneficial actions
specifically taken to address threats to the Franklin's bumble bee.
Oregon does not include invertebrates on their State endangered species
list (Oregon Department of Fish and Wildlife 2018, entire) and
California has no bee species included on its list of threatened and
endangered invertebrates (California Department of Fish and Wildlife
2018, entire). California has the Franklin's bumble bee listed on its
list of terrestrial and vernal pool invertebrates of conservation
priority but has no required actions or special protections associated
with the listing (California Department of Fish and Wildlife 2017, p.
10). The Franklin's bumble bee is on the species index for the U.S.
Forest Service and Bureau of Land Management Interagency Special
Status/Sensitive Species Program (ISSSSP). Although the Federal
agencies include the species in survey efforts and conduct general
meadow enhancement activities, there are no actions resulting from the
ISSSSP classification that address known threats to the Franklin's
bumble bee (ISSSSP 2018, entire).
General awareness of colony collapse disorder and increase of
conservation efforts for pollinators in general has likely had limited,
indirect effects on policies and regulations. The U.S. Forest Service
is working to include a section in all biological evaluations to
address the effects from agency actions on pollinators. In addition,
the Rogue River-Siskiyou National Forest is implementing ongoing
projects and mitigations to create and enhance pollinator habitat
(Colyer 2018, pers. comm.). The Oregon Department of Agriculture
restricts some potential sources of Nosema bombi from entering the
State for agricultural uses, including commercially produced colonies
of eastern bumble bee; only Bombus species native to Oregon are allowed
for commercial pollination purposes (Oregon Department of Agriculture
2017, p. 5). However, California allows, with appropriate permits, the
importation of eastern bumble bee, and other species such as the blue
orchard bee (Osmia lignaria), for greenhouse pollination (California
Department of Food and Agriculture 2017), making the potential for
pathogen spillover from nonnative bees higher in California.
Some local municipalities in Oregon enacted legislation against
aerial pesticide applications but none in the range of the Franklin's
bumble bee (Powell 2017, p. 1; City of Portland 2015, p. 2). However,
in the 2017 legislative session, Oregon passed an Avoidance of Adverse
Effects on Pollinating Insects law (Oregon Revised Statutes (ORS)
634.045) that is providing enhanced training of licensed and unlicensed
pesticide applicators in the State (Melathopoulos 2018, pers. comm.),
and could thereby reduce effects of pesticides on pollinators,
including Franklin's bumble bee.
In January 2017, the U.S. Environmental Protection Agency's Office
of Pesticide Programs published their ``Policy to Mitigate the Acute
Risk to Bees from Pesticide Products,'' which recommended new labeling
statements for pesticide products, including warnings for pesticides
with a known acute toxicity to bees (Tier 1 pesticides), including
neonicotinoids (specifically including imidacloprid, clothianidin, and
thiamethoxam) (U.S. Environmental Protection Agency 2017, p. 31). In
addition, the Environmental Protection Agency is working with State and
Tribal agencies to develop and implement local pollinator protection
plans, known as Managed Pollinator Protection Plans (MP3s). The
Environmental Protection Agency is promoting MP3s to address potential
pesticide exposure to bees and other pollinators at and beyond the site
of the application. However, States and Tribes have the flexibility to
determine the scope of pollinator protection plans that best responds
to pollinator issues in their regions. For example, State and Tribal
MP3s may address pesticide-related risks to all pollinators, including
managed bees and wild insect and non-insect pollinators (U.S.
Environmental Protection Agency 2018). The Service implemented a ban on
the use of
[[Page 47231]]
neonicotinoids on all lands in the National Wildlife Refuge System in
2014 (Service 2014); however, no refuge lands occur within the range of
the Franklin's bumble bee, and the Service rescinded the ban in 2018
(Service 2018b, entire). None of these aforementioned regulatory or
conservation measures has appreciably reduced or fully ameliorated
threats to the Franklin's bumble bee, as evidenced by the species'
acute and rangewide decline.
We note that, by using the SSA framework to guide our analysis of
the scientific information documented in the SSA report, we have not
only analyzed individual effects on the species, but we have also
analyzed their potential cumulative effects. We incorporate the
cumulative effects into our SSA analysis when we characterize the
current and future condition of the species. Our assessment of the
current status of the Franklin's bumble bee incorporates the threats
individually and cumulatively. Our assessment is iterative because it
accumulates and evaluates the effects of all the factors that may be
influencing the species, including threats and conservation efforts.
Because the SSA framework considers not just the presence of the
factors, but to what degree they collectively influence risk to the
entire species, our assessment integrates the cumulative effects of the
factors and replaces a standalone cumulative effects analysis.
Summary of Status
The significant decrease in abundance and distribution of the
Franklin's bumble bee to date has greatly reduced the species' ability
to adapt to changing environmental conditions and to guard against
further losses of adaptive diversity and potential extinction due to
catastrophic events. It also substantially reduced the ability of the
Franklin's bumble bee to withstand environmental variation,
catastrophic events, and changes in physical and biological conditions.
Coupled with the increased risk of extirpation due to the interaction
of reduced population size and the species' haplodiploid genetic
system, the Franklin's bumble bee may lack the resiliency required to
sustain populations into the future, even without further exposure to
pathogens and pesticides.
Summary of Comments and Recommendations
In our proposed rule published on August 13, 2019 (84 FR 40006), we
requested that all interested parties submit written comments on the
proposal by October 15, 2019. All comments we received are posted at
https://www.regulations.gov under Docket No. FWS-R1-ES-2018-0044. We
contacted appropriate Federal and State agencies (in both Oregon and
California), scientific experts and organizations, and other interested
parties and invited them to comment on the proposal, even if they
previously provided peer or partner review comments on the SSA report.
We did not receive any additional comments from individuals or agencies
who had previously provided peer review or partner review on the SSA
report. We did not receive any requests for a public hearing. We
reviewed all comments for substantive issues and new information
regarding the Franklin's bumble bee. During the comment period, we
received 53 letters or statements directly addressing the proposed
action, including one comment with 15,749 signatures (supporting the
listing of the Franklin's bumble bee). All but one of the commenters
supported the listing of the Franklin's bumble bee as endangered. All
but one of the commenters disagreed with our determination that
designating critical habitat is not prudent. Substantive comments we
received during the comment period are addressed below and, where
appropriate, are incorporated directly into this final rule.
Public Comments
(1) Comment: Several commenters disagreed with our conclusion that
Franklin's bumble bees are habitat generalists. Commenters stated that
the limited range of the species demonstrates that it is only found in
specific habitats and that if the species was truly a habitat
generalist, it would be expected to have a much larger range. They
noted that the range of the species is limited to the Siskiyou
Mountains, a subset of the Klamath Mountain region of southern Oregon
and southwestern California, and that there are specific
characteristics of Franklin's bumble bee habitat in that area that can
be identified, such as montane meadows rich in lupine, California
poppy, mountain monardella, and clover. Commenters note that the
Siskiyou Range is known for its high number of endemic species and
these other endemic species are not considered habitat generalists.
Our Response: As stated in the SSA report, our analyses are
predicated on multiple assumptions due to the significant lack of
species-specific information for Franklin's bumble bee (2018a, p. 6).
We further note that for the purposes of the analyses in the SSA
report, we rely heavily on information from closely-related species
from the same sub-genus, Bombus sensu stricto, particularly the rusty
patched bumble bee and the western bumble bee. The range of the western
bumble bee completely overlaps the historical range of Franklin's
bumble bee, and the western bumble bee is still found at several known
Franklin's bumble bee locations, most recently in 2019 at Mt. Ashland,
the last known location of Franklin's bumble bee. As mentioned in the
August 13, 2019, proposed rule (84 FR 40006) and the SSA report, a
specific habitat study for the species has not been completed, nor have
the specific life-history characteristics and behavior of this rare
species been studied. Despite uncertainties regarding the Franklin's
bumble bee's habitat needs, we know they need (1) floral resources for
nectaring throughout the colony cycle, and (2) relatively protected
areas for breeding and shelter. The habitat elements appearing to
fulfill those needs that have documented use by the Franklin's bumble
bee are relatively plentiful and widely distributed.
In our expert elicitation, we asked the following question: In
looking at the distribution map of all known occurrences of Franklin's
bumble bee, are there areas in Douglas, Jackson, Josephine, Siskiyou,
and Trinity Counties in addition to these occurrence sites that might
contain the species' known foraging plants: Lupine (Lupinus spp.),
California poppy (Eschscholzia californica), horsemint or nettle-leaf
giant hyssop (Agastache urticifolia), and mountain monardella
(Monardella odoratissima)? Dr. Thorp (the preeminent authority on
Franklin's bumble bee) responded that he was ``trying to figure out
what defined or limited habitat at the time that [the species]
disappeared.'' Dr. Thorp noted that the species had historically ranged
from 500 ft in elevation at Sutherland to over 6,700 ft at Mt. Shasta
and Mt. Ashland, meaning they could go through multiple mountain passes
to extend east or south, but they did not; they were not limited by
geography. Further, they were also not limited by flowering plants;
they are generalist foragers (Thorp 2018, pers. comm). In addition,
bumble bees ``are classic generalist foragers, capable of working a
wide variety of plants for their resources'' (Williams et al. 2014, p.
15). The historical record also suggests the Franklin's bumble bee may
use a variety of nesting substrates given that a colony was found in a
residential garage in Medford, Oregon (Thorp 2017, pers. comm.).
[[Page 47232]]
We agree that the Klamath-Siskiyou ecoregion, which hosts much of
the historical range of the Franklin's bumble bee, is very diverse and
relatively rich in endemic species. The Klamath-Siskiyou ecoregion is
considered a global center of biodiversity, is an International Union
for Conservation of Nature (IUCN) Area of Global Botanical Significance
(1 of 7 in North America), and is proposed as a World Heritage Site and
United Nations Educational, Scientific and Cultural Organization
(UNESCO) Biosphere Reserve (World Wildlife Fund 2020, entire).
Extensive literature is available describing some of the biologic
investigations in this ecoregion (University of Oregon 2020, entire).
However, we are not aware of any information linking Franklin's bumble
bee exclusively to endemic habitat features, including floral resources
specific to this ecosystem.
(2) Comment: One commenter noted that forage is only one component
of Franklin's bumble bee's niche and does not alone define a habitat
generalist, citing Devictor et al. 2010. They stated that even if the
species is a general forager it could still have a relatively narrow
habitat niche, adding that narrow pollen diets are associated with
other rare bumble bees like Franklin's bumble bee. They referenced a
recent study, Wood et al. 2019, that looked at the diets of two species
closely related to Franklin's bumble bee, the American bumble bee and
rusty patch bumble bee, and found these declining species had a narrow
pollen diet, collecting around one-third fewer pollen types than other
more stable species. The study further noted that these two species are
short-tongued and the anatomical feature was mentioned as a potential
factor in their narrower diet.
Our Response: There are many factors related to Franklin's bumble
bees and their habitat that we do not yet, and may never, understand;
however, the information gathered for our assessment, including the
opinion of the preeminent authority on the species (Dr. Robbin Thorp),
indicates that Franklin's bumble bee is likely a habitat generalist.
The commenter cites Devictor et al. 2010, when noting forage is only
one component of Franklin's bumble bee's niche and may not alone define
a habitat generalist. However, the same paper also states that a
measure of ecological specialization is the assumption that specialists
should co-occur with relatively few species; this is in contrast to
generalist species who should co-occur with many different species
across sites (Devictor et al. 2010, p. 23), as has been observed with
Franklin's bumble bees.
We agree that narrow pollen diets likely play a role in the decline
of some Bombus species as the distribution and abundance of their
floral resources change, but we do not have sufficient information to
determine if this was a significant causal factor in the decline of the
Franklin's bumble bee. We do have some records of the species of plants
visited by Franklin's bumble bee, but we do not have an exhaustive or
comprehensive list. Of the plants Franklin's bumble bee is known to
use, many are widely distributed. For example, California poppy is
found in Oregon, Washington, Nevada, Arizona, Minnesota, and
northwestern Baja California, Mexico. Nettle-leaf giant hyssop (horse
mint) is native throughout western North America from British Columbia
in Canada, to California to Colorado, where it grows in a wide variety
of habitat types. Mountain monardella is found in montane forests
between 600 m and 3,100 m (1,969 ft and 10,170 ft) in elevation in
Oregon, Washington, Nevada, and Utah. Regarding tongue length, although
the Franklin's bumble bee is a short-tongued species, Wood et al. found
no evidence of tongue length as a predictor of dietary breadth (2019,
p. 9).
(3) Comment: Several commenters disagreed that the present or
threatened destruction, modification, or curtailment of habitat is not
a threat to the Franklin's bumble bee. One commenter stated that the
Service analyzed fire suppression, agricultural intensification, urban
development, livestock grazing, and effects of climate change, but only
as to whether they contributed to the historical decline of Franklin's
bumble bee, not as current threats. One commenter stated that the
climate change effects of increased drought severity, wildfire risk,
and winter or early season flood risk are clear threats to Franklin's
bumble bee habitat in the current and near future; they noted that
flood risk is especially concerning for overwintering hibernating
queens who may suffer mortality or respond by emerging too early for
floral resources. The commenter also noted that due to the myriad of
threats outlined in the August 13, 2019, proposed rule (84 FR 40006),
it is incorrect to conclude that Franklin's bumble bee's habitat is
unlimited in its capacity to provide uncontaminated resources to the
species. One commenter stated that all-terrain vehicle (ATV) use and
herbicide use are current threats to Franklin's bumble bee's habitat,
but provided no additional information upon which to base those claims.
Our Response: In our analysis of the threats facing Franklin's
bumble bee in the SSA report, we completed a review of the best
available scientific and commercial information on threats that have
been present in the range of the bee (Service 2018a, pp. 23-40). During
the public comment period on the proposed rule we did not receive any
new information regarding potential threats that prompted us to change
the conclusions in our analysis. The viability analysis takes into
account the threats to the species that have influenced historical
populations, threats that are influencing the current condition of
populations, and threats which are likely to play a role in the
species' overall viability into the future. In our SSA report for
Franklin's bumble bee, we noted those threats that are likely to play a
role in the future (pathogens, pesticides, and the synergistic effects
of small population size), but did not complete a full future condition
analysis; the dearth of information on this species, particularly the
lack of species occurrence information after 2006, limited our ability
to compare current and future condition.
Although empirical data are currently unavailable regarding the
level of habitat loss and degradation specifically affecting the
Franklin's bumble bee, we do know that habitat impacts have caused the
decline of other Bombus species (e.g., Goulson et al. 2015, p. 2;
Goulson and Darvill 2008, pp. 193-194; Brown and Paxton 2009, pp. 411-
412). Although habitat loss has had negative effects on Bombus species
in general, available information did not indicate it was a driver of
the decline of Franklin's bumble bee. Habitat appears generally intact
and in good condition throughout the known historical locations of the
Franklin's bumble bee and in all recent focused survey areas, and many
of these habitats currently host a wide variety of other bumble bees,
including closely-related species like the western bumble bee. As noted
above in Summary of Biological Status and Threats, we have no
information to suggest that any known Franklin's bumble bee locations
were in the path of wildfire at the time those locations were occupied.
Further, as made evident in our geographic information system (GIS)
analysis, most of the recent locations with confirmed Franklin's bumble
bee observations are on publicly owned land that is managed to preserve
habitat conditions through a variety of mechanisms, including fire
suppression. Furthermore, we have no information to suggest that
habitat destruction or modification from fire
[[Page 47233]]
suppression, agricultural intensification, urban development, and
livestock grazing will increase in intensity to the point where they
will be threats to the viability of the species in the future (Bureau
of Land Management 2016, p. 103; Portland State University 2015, p. 7;
U.S. Forest Service 1989, IV-87 to IV-90, IV-113 to IV-119; U.S. Forest
Service 1990, pp. 4-149 to 4-179; Service 2018a, p. 32).
Future changes in temperature and precipitation may lead to changes
in the vegetation community in Franklin's bumble bee habitat. However,
as a habitat generalist, Franklin's bumble bee appears to forage on a
variety of floral resources, and we have no information to suggest that
they would not seek the nectar of whatever floral resource was in bloom
at the time they emerge from their nests. Additionally, the risk of
catastrophic wildfire and seasonal flooding, as well as other effects
from storm events, are naturally present in the ecosystems within the
range of the Franklin's bumble bee. The effects of climate change may
affect the frequency and intensity of these events, thereby affecting
the availability of floral resources, the suitability of nest
locations, and the survival of overwintering queens. However, we cannot
project the likelihood of when or where these events will occur, or how
intense they will be if they do occur.
We agree that Franklin's bumble bee habitat is not unlimited. As we
point out in the beginning of the SSA report, Franklin's bumble bee is
the most narrowly endemic bumble bee in North America, and possibly the
world. In accordance with listing Franklin's bumble bee as endangered
under the Act, we will develop a recovery outline for this species.
Current and possible future threats will be considered during recovery
planning for this species.
(4) Comment: One commenter disagreed that critical habitat could
not be defined. They point to our proposed rule, which states that
surveys have been done in areas that appear to have good habitat for
Bombus and Franklin's bumble bee, as evidence that there are known and
defined characteristics of potential critical habitat in previously
occupied areas.
Our Response: While we acknowledge that some general habitat
associations of Bombus are known, the Franklin's bumble bee has been
found in a wide array of habitat types, from foraging in montane
meadows in a remote wilderness area of California to nesting in a
residential garage in the city limits of Medford, Oregon. Furthermore,
elevation does not appear to limit the species' dispersal capabilities.
No habitat study for the Franklin's bumble bee has been completed; such
a study was initiated in 2006, when the Franklin's bumble bee was last
seen, but could not continue due to the subsequent absence of the
species. As such, we cannot with specificity articulate the physical or
biological features essential to the conservation of the Franklin's
bumble bee, or determine whether or not any area would meet the
definition of critical habitat for the Franklin's bumble bee (see
discussion under Prudency Determination, below).
Even if physical and biological features can be articulated for the
species, the regulations in effect at the time the species was proposed
for listing indicated that we may find that designating critical
habitat is not prudent if it is not beneficial to the species. With the
exception of the inundation of two sites with older historical
occurrences of Franklin's bumble bee locations by the construction of
Applegate Dam, and a report of soil modification on a portion of the
Gold Hill site 4 years after the last occurrence of Franklin's bumble
bee in the area, no noticeable destruction, modification, or
curtailment of habitat or range can be identified in areas where the
species had been previously located. No significant destruction or
modification of Franklin's bumble bee habitat can be attributed to
natural fire, prescribed fire, agricultural intensification, urban
development, livestock grazing, or the effects of climate change.
Additionally, as discussed above, the Franklin's bumble bee has been
documented using a wide variety of habitats throughout its range.
Because habitat for the Franklin's bumble bee is not limiting, and
because the bee is considered to be flexible with regards to its
habitat, the availability of habitat does not limit the conservation of
the Franklin's bumble bee now, nor will it in the future (see response
to Comment (3)). Therefore, we have determined that designation of
critical habitat for the Franklin's bumble bee is not beneficial to the
species and, therefore, not prudent.
(5) Comment: Two commenters disagreed that the designation of
critical habitat would not be beneficial to the conservation of the
species. They argue it would be beneficial due to the following: (1)
Critical habitat would promote connectivity between habitat patches,
which will help reduce the risk of inbreeding depression and promote
recovery of the species; (2) many studies have shown the link between
quality habitat and nutrition and health of bumble bee colonies, and
critical habitat would be beneficial because it would give Franklin's
bumble bee access to more high-quality habitat to combat the threats of
pathogens and pesticides and to recover from them; (3) competition and
disease from nonnative honey bees, as well as pesticides from both
agriculture and siliviculture, are threats that will be unregulated
without the designation of critical habitat; (4) critical habitat would
provide concrete objective locations in which to protect the species
through section 7 of the Act; and (5) critical habitat would inform the
species recovery plan and where exactly the Service would implement
recovery actions to ameliorate threats to the species.
Our Response: The implementing regulations of the Act upon which
the August 13, 2019, proposed rule (84 FR 40006) and this final rule
are based set forth that the factors the Service may consider in
determining that a critical habitat designation would not be prudent
include, but are not limited to, whether the species is threatened by
taking or other human activity, and identification of critical habitat
can be expected to increase the degree of threat to the species; or
whether such designation of critical habitat would not be beneficial to
the species (50 CFR 424.12(a)(1)). We determine that the designation of
critical habitat would not be beneficial to the species because the
present or threatened destruction, modification, or curtailment of the
species' habitat or range (Factor A) is not a threat to the Franklin's
bumble bee and because we cannot with specificity articulate the
physical or biological features essential to the conservation of the
Franklin's bumble bee, or determine whether or not any area would meet
the definition of critical habitat for the Franklin's bumble bee (see
discussion under Prudency Determination, below).
As mentioned in our response to Comments (3) and (4), no noticeable
destruction, modification, or curtailment of Franklin's bumble bee
habitat or range can be identified in areas where the species had been
previously located, and could not be shown to have affected the
resiliency of any population of Franklin's bumble bee. None of the
potential threats to Franklin's bumble bee habitat we assessed appears
to threaten the viability of the species (USFWS 2018a, pp. 23-41).
Therefore, we find that because the present or threatened destruction,
modification, or curtailment of a species' habitat or range is not a
threat to Franklin's bumble bee, designating critical habitat is not
beneficial and, therefore, not prudent.
Furthermore, regarding section 7 consultation, because of the
listing of
[[Page 47234]]
the species (absent critical habitat), Federal agencies will still be
required to consult under section 7 of the Act on activities that may
affect this species in areas where the Franklin's bumble bee is
reasonably certain to occur. The Federal action agency will be required
to identify any listed species that could be within the project area of
any proposed activity, and consult with the Service if that activity is
likely to adversely affect the species.
Determination of the Status of Franklin's Bumble Bee
Section 4 of the Act (16 U.S.C. 1533) and its implementing
regulations (50 CFR part 424) set forth the procedures for determining
whether a species meets the definition of an endangered species or a
threatened species. The Act defines an ``endangered species'' as a
species that is ``in danger of extinction throughout all or a
significant portion of its range,'' and a ``threatened species'' as a
species that is ``likely to become an endangered species within the
foreseeable future throughout all or a significant portion of its
range.'' The Act requires that we determine whether a species meets the
definition of ``endangered species'' or ``threatened species'' because
of any of the following factors: (A) The present or threatened
destruction, modification, or curtailment of its habitat or range; (B)
overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; or (E) other natural or manmade factors
affecting its continued existence.
Status Throughout All of Its Range
We evaluated the past, present, and future threats to the
Franklin's bumble bee and assessed the cumulative effect of the threats
under the Act's section 4(a)(1) factors. Our assessment did not find
habitat loss or modification (Factor A) to be the cause of the decline
of the Franklin's bumble bee, and we have no information to suggest
that habitat destruction or modification will increase in intensity in
the near future. There is no indication that the Franklin's bumble bee
was at risk of overutilization for commercial, recreational,
scientific, or educational purposes (Factor B). Known pathogens occur
within the historical range of the Franklin's bumble bee, and we have
evidence of several pathogens (Factor C) infecting closely related
species within that range. Although we do not have direct evidence of
pathogens playing a role in the decline of the Franklin's bumble bee,
the disappearance of the Franklin's bumble bee occurred soon after a
period of introduction of new pathogens. Furthermore, documented
effects to other closely related species lead many species experts to
suspect that the effects of pathogens had some connection to the
decline of the Franklin's bumble bee. We evaluated existing regulatory
mechanisms (Factor D) and conservation measures and their effects on
the threats and the status of the Franklin's bumble bee; we found that
the existing regulatory mechanisms or conservation measures in place do
not appreciably reduce or ameliorate the existing threats to the
species, as evidenced by the species' acute and rangewide decline.
Although we have no direct evidence that pesticide use contributed to
the decline of the Franklin's bumble bee, confirmed effects to other
closely related Bombus species suggest that pesticide use (Factor E)
was likely a factor in the decline of the Franklin's bumble bee.
Additionally, given the historically small population size (Factor E)
of the Franklin's bumble bee and its haplodiploid genetic system, it is
more vulnerable to extirpation than other species, and it is likely the
genetic system and the rarity of this species contributed to the
decline of the Franklin's bumble bee (Factor E).
The combination of multiple threats is typically more harmful than
any one acting alone, and it is likely that several of the threats
mentioned above acted cumulatively and synergistically on the
Franklin's bumble bee. Pathogens in combination with pesticides, as
well as pathogens in combination with the effects of small population
size, may have hastened and amplified the decline of the Franklin's
bumble bee to a greater degree than any one of the three factors caused
on its own. Although the ultimate source of the decline is unknown, the
acute and rangewide decline of the Franklin's bumble bee is
undisputable.
The Act defines an ``endangered species'' as any species that is in
danger of extinction throughout all or a significant portion of its
range, and a ``threatened species'' as any species that is likely to
become endangered within the foreseeable future throughout all or a
significant portion of its range. We find that, based on the severity
and immediacy of threats currently affecting the species, the
Franklin's bumble bee meets the definition of an endangered species.
The threats of pathogens, pesticides, and small population size are
ongoing and rangewide; they will continue to act individually and in
combination to decrease the resiliency, redundancy, and representation
of the Franklin's bumble bee. The risk of extinction is high because
the species has not been found since 2006, and the suspected threats to
the species persist. We find that a threatened species status is not
appropriate for the Franklin's bumble bee because of the extreme loss
of abundance of the species, because the threats are occurring
rangewide and are not localized, and because the threats are ongoing
and expected to continue into the future. Thus, after assessing the
best available information, we determine that the Franklin's bumble bee
is in danger of extinction throughout all of its range.
Status Throughout a Significant Portion of Its Range
Under the Act and our implementing regulations, a species may
warrant listing if it is in danger of extinction or likely to become so
in the foreseeable future throughout all or a significant portion of
its range. We have determined that the Franklin's bumble bee is in
danger of extinction throughout all of its range and accordingly did
not undertake an analysis of whether there are any significant portions
of its range. Because Franklin's bumble bee warrants listing as
endangered throughout all of its range, our determination is consistent
with the decision in Center for Biological Diversity v. Everson, 2020
WL 437289 (D.D.C. Jan. 28, 2020), in which the court vacated only the
aspect of our July 1, 2014, Final Policy on Interpretation of the
Phrase ``Significant Portion of Its Range'' in the Endangered Species
Act's Definitions of ``Endangered Species'' and ``Threatened Species''
(79 FR 37578) that provided the Services do not undertake an analysis
of significant portions of a species' range if the species warrants
listing as threatened throughout all of its range.
Determination of Status
Our review of the best available scientific and commercial
information indicates that the Franklin's bumble bee meets the
definition of an endangered species. Therefore, we are listing the
Franklin's bumble bee as an endangered species in accordance with
sections 3(6) and 4(a)(1) of the Act. Although this species has not
been observed since 2006, we conclude it is premature at this time to
determine that the species is extinct absent a more thorough survey
effort. We recommend expanded survey efforts to help verify the status
of this species.
[[Page 47235]]
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened species under the Act include recognition, recovery actions,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing results in public awareness, and
conservation by Federal, State, Tribal, and local agencies; private
organizations; and individuals. The Act encourages cooperation with
States and other countries and calls for recovery actions to be carried
out for listed species. The protection required by Federal agencies and
the prohibitions against certain activities are discussed, in part,
below.
Recovery Actions
The primary purpose of the Act is the conservation of endangered
and threatened species and the ecosystems upon which they depend. The
ultimate goal of such conservation efforts is the recovery of these
listed species, so that they no longer need the protective measures of
the Act. Subsection 4(f) of the Act calls for the Service to develop
and implement recovery plans for the conservation of endangered and
threatened species. The recovery planning process involves the
identification of actions that are necessary to halt or reverse a
species' decline by addressing the threats to its survival and
recovery. The goal of this process is to restore listed species to a
point where they are secure, self-sustaining, and functioning
components of their ecosystems.
Recovery planning includes the development of a recovery outline
shortly after a species is listed, and preparation of a draft and final
recovery plan. The recovery outline guides the immediate implementation
of urgent recovery actions and describes the process we will use to
develop a recovery plan. Revisions of the plan may be done to address
continuing or new threats to the species, as new substantive
information becomes available. The recovery plan also identifies
recovery criteria for review of when a species may be ready for
reclassification from endangered to threatened (``downlisting'') or
removal from protected status (``delisting''), and methods for
monitoring recovery progress. Recovery plans also establish a framework
for agencies to coordinate their recovery efforts and provide estimates
of the cost of implementing recovery tasks. Recovery teams (composed of
species experts, Federal and State agencies, nongovernmental
organizations, and stakeholders) are often established to develop
recovery plans. When completed, the recovery outline, draft recovery
plan, and the final recovery plan will be available on our website
(https://www.fws.gov/endangered), or from our Oregon Fish and Wildlife
Office (see FOR FURTHER INFORMATION CONTACT).
Implementation of recovery actions generally requires the
participation of a broad range of partners, including other Federal
agencies, States, Tribes, nongovernmental organizations, businesses,
and private landowners. Examples of recovery actions include habitat
restoration (e.g., restoration of native vegetation), research, captive
propagation and reintroduction, and outreach and education. The
recovery of many listed species cannot be accomplished solely on
Federal lands because their range may occur primarily or solely on non-
Federal lands. To achieve recovery of these species requires
cooperative conservation efforts on private, State, and tribal lands.
Following publication of this final listing rule, funding for
recovery actions will be available from a variety of sources, including
Federal budgets, State programs, and cost share grants for non-Federal
landowners, the academic community, and nongovernmental organizations.
In addition, pursuant to section 6 of the Act, the States of Oregon and
California will be eligible for Federal funds to implement management
actions that promote the protection or recovery of the Franklin's
bumble bee. Information on our grant programs that are available to aid
species recovery can be found at: https://www.fws.gov/grants.
Please let us know if you are interested in participating in
recovery efforts for the Franklin's bumble bee. Additionally, we invite
you to submit any new information on this species whenever it becomes
available and any information you may have for recovery planning
purposes (see FOR FURTHER INFORMATION CONTACT).
Regulatory Provisions
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is proposed or listed as an
endangered or threatened species and with respect to its critical
habitat, if any is designated. Regulations implementing this
interagency cooperation provision of the Act are codified at 50 CFR
part 402. Section 7(a)(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 any endangered or
threatened species or destroy or adversely modify its critical habitat.
If a Federal action may affect a listed species or its critical
habitat, the responsible Federal agency must enter into consultation
with the Service.
Federal agency actions within the species' habitat that may require
conference or consultation or both include management and any other
landscape-altering activities on Federal lands administered by the U.S.
Forest Service and Bureau of Land Management, the National Park
Service, and the Bureau of Reclamation; technical assistance and
projects funded through the U.S. Department of Agriculture Natural
Resources Conservation Service; issuance of section 404 Clean Water Act
(33 U.S.C. 1251 et seq.) permits by the U.S. Army Corps of Engineers,
and construction and maintenance of roads or highways by the Federal
Highway Administration.
The Act and its implementing regulations set forth a series of
general prohibitions and exceptions that apply to endangered wildlife.
The prohibitions of section 9(a)(1) of the Act, codified at 50 CFR
17.21, make it illegal for any person subject to the jurisdiction of
the United States to take (which includes harass, harm, pursue, hunt,
shoot, wound, kill, trap, capture, or collect; or to attempt any of
these) endangered wildlife within the United States or on the high
seas. In addition, it is unlawful to import; export; deliver, receive,
carry, transport, or ship in interstate or foreign commerce in the
course of commercial activity; or sell or offer for sale in interstate
or foreign commerce any species listed as an endangered species. It is
also illegal to possess, sell, deliver, carry, transport, or ship any
such wildlife that has been taken illegally. Certain exceptions apply
to employees of the Service, the National Marine Fisheries Service,
other Federal land management agencies, and State conservation
agencies.
We may issue permits to carry out otherwise prohibited activities
involving endangered wildlife under certain circumstances. Regulations
governing permits are codified at 50 CFR 17.22. With regard to
endangered wildlife, a permit may be issued for the following purposes:
For scientific purposes, to enhance the propagation or survival of the
species, and for incidental take in connection with otherwise lawful
activities. There are also certain statutory exemptions from the
prohibitions, which are found in sections 9 and 10 of the Act.
It is our policy, as published in the Federal Register on July 1,
1994 (59 FR 34272), to identify to the maximum extent practicable at
the time a species
[[Page 47236]]
is listed, those activities that would or would not constitute a
violation of section 9 of the Act. The intent of this policy is to
increase public awareness of the effect of a listing on proposed and
ongoing activities within the range of the listed species. Based on the
best available information, the following actions are unlikely to
result in a violation of section 9 of the Act if these activities are
carried out in accordance with existing regulations and permit
requirements; this list is not comprehensive:
(1) Recreation, specifically skiing at Mt. Ashland, and use of the
Pacific Crest Trail;
(2) Timber sales; and
(3) Livestock grazing.
Based on the best available information, the following actions may
potentially result in a violation of section 9 of the Act if they are
not authorized in accordance with applicable law; this list is not
comprehensive:
(1) Unauthorized handling or collecting of the Franklin's bumble
bee;
(2) Unauthorized release of biological control agents that attack
any life stage of the Franklin's bumble bee, including the unauthorized
use of herbicides, pesticides, or other chemicals in areas in which the
Franklin's bumble bee is known to occur (i.e., in the Franklin's bumble
bee's historical range); and
(3) Unauthorized release of nonnative species or native species
that carry pathogens, diseases, or fungi that are known or suspected to
adversely affect the Franklin's bumble bee where the species is known
to occur (i.e., in the Franklin's bumble bee's historical range).
Questions regarding whether specific activities would constitute a
violation of section 9 of the Act should be directed to the Oregon Fish
and Wildlife Office (see FOR FURTHER INFORMATION CONTACT).
II. Critical Habitat
Background
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
(a) Essential to the conservation of the species, and
(b) Which may require special management considerations or
protection; and
(2) Specific areas outside the geographical area occupied by the
species at the time it is listed, upon a determination that such areas
are essential for the conservation of the species.
Our regulations at 50 CFR 424.02 define ``geographical area
occupied by the species'' as an area that may generally be delineated
around species' occurrences, as determined by the Secretary (i.e.,
range). Such areas may include those areas used throughout all or part
of the species' life cycle, even if not used on a regular basis (e.g.,
migratory corridors, seasonal habitats, and habitats used periodically,
but not solely by vagrant individuals).
Conservation, as defined under section 3 of the Act, means to use
and the use of all methods and procedures that are necessary to bring
an endangered or threatened species to the point at which the measures
provided pursuant to the Act are no longer necessary. Such methods and
procedures include, but are not limited to, all activities associated
with scientific resources management such as research, census, law
enforcement, habitat acquisition and maintenance, propagation, live
trapping, and transplantation, and, in the extraordinary case where
population pressures within a given ecosystem cannot be otherwise
relieved, may include regulated taking.
Critical habitat receives protection under section 7 of the Act
through the requirement that Federal agencies ensure, in consultation
with the Service, that any action they authorize, fund, or carry out is
not likely to result in the destruction or adverse modification of
critical habitat. The designation of critical habitat does not affect
land ownership or establish a refuge, wilderness, reserve, preserve, or
other conservation area. Such designation does not allow the government
or public to access private lands. Such designation does not require
implementation of restoration, recovery, or enhancement measures by
non-Federal landowners. Where a landowner requests Federal agency
funding or authorization for an action that may affect a listed species
or critical habitat, the Federal agency would be required to consult
with the Service under section 7(a)(2) of the Act. However, even if the
Service were to conclude that the proposed activity would result in
destruction or adverse modification of the critical habitat, the
Federal action agency and the landowner are not required to abandon the
proposed activity, or to restore or recover the species; instead, they
must implement ``reasonable and prudent alternatives'' to avoid
destruction or adverse modification of critical habitat.
Under the first prong of the Act's definition of critical habitat,
areas within the geographical area occupied by the species at the time
it was listed are included in a critical habitat designation if they
contain physical or biological features (1) which are essential to the
conservation of the species and (2) which may require special
management considerations or protection. For these areas, critical
habitat designations identify, to the extent known using the best
scientific and commercial data available, those physical or biological
features that are essential to the conservation of the species (such as
space, food, cover, and protected habitat). In identifying those
physical or biological features within an area, we focus on the
specific features that support the life-history needs of the species,
including, but not limited to, water characteristics, soil type,
geological features, prey, vegetation, symbiotic species, or other
features. A feature may be a single habitat characteristic, or a more
complex combination of habitat characteristics. Features may include
habitat characteristics that support ephemeral or dynamic habitat
conditions. Features may also be expressed in terms relating to
principles of conservation biology, such as patch size, distribution
distances, and connectivity.
Under the second prong of the Act's definition of critical habitat,
we can designate critical habitat in 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. We determine whether unoccupied areas are essential for the
conservation of the species by considering the life-history, status,
and conservation needs of the species. This is further informed by any
generalized conservation strategy, criteria, or outline that may have
been developed for the species to provide a substantive foundation for
identifying which features and specific areas are essential to the
conservation of the species and, as a result, to the development of the
critical habitat designation. For example, an area currently occupied
by the species but that was not occupied at the time of listing may be
essential to the conservation of the species and may be included in the
critical habitat designation.
Section 4 of the Act requires that we designate critical habitat on
the basis of the best scientific data available. Further, our Policy on
Information Standards Under the Endangered Species Act (published in
the Federal Register on July 1, 1994 (59 FR 34271)),
[[Page 47237]]
the Information Quality Act (section 515 of the Treasury and General
Government Appropriations Act for Fiscal Year 2001 (Pub. L. 106-554;
H.R. 5658)), and our associated Information Quality Guidelines, provide
criteria, establish procedures, and provide guidance to ensure that our
decisions are based on the best scientific data available. They require
our biologists, to the extent consistent with the Act and with the use
of the best scientific data available, to use primary and original
sources of information as the basis for recommendations to designate
critical habitat.
Prudency Determination
Section 4(a)(3) of the Act, as amended, and implementing
regulations (50 CFR 424.12), require that, to the maximum extent
prudent and determinable, the Secretary shall designate critical
habitat at the time the species is determined to be an endangered or
threatened species.
On August 27, 2019, the Service published a final rule (84 FR
45020) revising the regulations at 50 CFR part 424 for listing species
and designating critical habitat. However, the revisions apply only to
relevant rulemakings for which the proposed rule is published after
September 26, 2019, the effective date of the final rule. Thus, the
prior version of the regulations at 50 CFR part 424 continues to apply
to any rulemakings for which a proposed rule was published before
September 26, 2019, including this final rule for Franklin's bumble
bee.
The prior version of the regulations at 50 CFR part 424 (50 CFR
424.12(a)(1)) state that the designation of critical habitat is not
prudent when one or both of the following situations exist:
(1) The species is threatened by taking or other human activity,
and identification of critical habitat can be expected to increase the
degree of threat to the species, or
(2) Such designation of critical habitat would not be beneficial to
the species. In determining whether a designation would not be
beneficial, the factors the Services may consider includes whether the
present or threatened destruction, modification, or curtailment of a
species' habitat or range is not a threat to the species.
As discussed above in the threats analysis, there is currently no
imminent threat of take attributed to collection or vandalism
identified under Factor B for this species, and identification and
mapping of critical habitat is not expected to initiate any such
threat. In the absence of finding that the designation of critical
habitat would increase threats to a species, we next determine whether
such designation of critical habitat would be beneficial to the
Franklin's bumble bee. For the reasons discussed below, we have
determined that designating critical habitat would not be beneficial.
Designating Habitat Would Not Be Beneficial to the Species
The Franklin's bumble bee was widely distributed throughout its
range and considered flexible with regard to habitat requirements. We
know that the Franklin's bumble bee needs (1) floral resources for
nectaring throughout the colony cycle, and (2) relatively protected
areas for breeding and shelter. In addition, because the best available
scientific information indicates that the Franklin's bumble bee is a
generalist forager, its habitat preferences and needs are relatively
plentiful and widely distributed. While Bombus species in general might
prefer protected meadows with an abundance of wildflowers, the
Franklin's bumble bee has been found in a wide array of habitat types,
from foraging in montane meadows in a remote wilderness area of
California to nesting in a residential garage in the city limits of
Medford, Oregon. The species has a broad elevational range from 162 m
(540 ft) to 2,340 m (7,800 ft); elevation does not appear to limit the
species' dispersal capabilities.
Some general habitat associations of Bombus are known; however, as
one of the rarest Bombus species, the Franklin's bumble bee is somewhat
enigmatic and a specific habitat study for the Franklin's bumble bee
has not been completed. Such a study was initiated in 2006, when the
Franklin's bumble bee was last seen, but could not continue due to the
subsequent absence of the species. Therefore, we cannot with
specificity articulate the physical or biological features essential to
the conservation of the Franklin's bumble bee, or determine whether or
not any area would meet the definition of critical habitat for the
Franklin's bumble bee.
Since it was first identified in 1921, the Franklin's bumble bee
appears to have always been a rare species with a limited range. In
fact, the species has perhaps the most limited range of any Bombus
species in the world. Nonetheless, Franklin's bumble bee habitat is not
known to be limiting, and habitat loss is not a threat to the species.
With the exception of the inundation of two sites with older historical
occurrences of Franklin's bumble bee (through the construction of
Applegate Dam, and a report of soil modification on a portion of the
Gold Hill site 4 years after the last occurrence of Franklin's bumble
bee in the area), no noticeable destruction, modification, or
curtailment of habitat or range can be identified in areas where the
species had been previously located. No significant destruction or
modification of Franklin's bumble bee habitat can be attributed to
natural fire, prescribed fire, agricultural intensification, urban
development, livestock grazing, or the effects of climate change.
Additionally, as discussed above, the Franklin's bumble bee has been
documented using a wide variety of habitats throughout its range.
Because habitat for the Franklin's bumble bee is not limiting, and
because the bee is considered to be flexible with regards to its
habitat, the availability of habitat does not limit the conservation of
the Franklin's bumble bee now, nor will it in the foreseeable future.
In the Service and National Marine Fisheries Service's response to
comments on the February 11, 2016, final rule (81 FR 7414) revising the
critical habitat regulations (the regulations in effect at the time the
Franklin's bumble bee was proposed for listing), the Services expressly
contemplated a fact pattern where designating critical habitat may not
be beneficial to the species: ``[I]n some circumstances, a species may
be listed because of factors other than threats to its habitat or
range, such as disease, and the species may be a habitat generalist. In
such a case, on the basis of the existing and revised regulations, it
is permissible to determine that critical habitat is not beneficial
and, therefore, not prudent'' (81 FR 7425). This is the fact pattern we
are presented with in the case of the Franklin's bumble bee. In view of
the foregoing, we conclude that present or threatened destruction,
modification, or curtailment of habitat is not a threat to the
Franklin's bumble bee; rather, disease and other manmade factors are
likely the primary threat to the species within its habitat. Therefore,
in accordance with 50 CFR 424.12(a)(1), we determine that critical
habitat is not beneficial and, therefore, not prudent for the
Franklin's bumble bee.
Required Determinations
National Environmental Policy Act (42 U.S.C. 4321 et seq.)
We have determined that environmental assessments and environmental
impact statements, as defined under the authority of the National
Environmental Policy Act (NEPA; 42 U.S.C. 4321 et seq.), need not be
prepared in connection with listing a species as an endangered or
threatened species under the
[[Page 47238]]
Endangered Species Act. We published a notice outlining our reasons for
this determination in the Federal Register on October 25, 1983 (48 FR
49244).
Government-To-Government Relationship With Tribes
In accordance with the President's memorandum of April 29, 1994
(Government-to-Government Relations with Native American Tribal
Governments; 59 FR 22951), Executive Order 13175 (Consultation and
Coordination With Indian Tribal Governments), and the Department of the
Interior's manual at 512 DM 2, we acknowledge our responsibility to
communicate meaningfully with recognized Federal Tribes on a
government-to-government basis. In accordance with Secretarial Order
3206 of June 5, 1997 (American Indian Tribal Rights, Federal-Tribal
Trust Responsibilities, and the Endangered Species Act), we acknowledge
our responsibilities to work directly with tribes in developing
programs for healthy ecosystems, to acknowledge that tribal lands are
not subject to the same controls as Federal public lands, to remain
sensitive to Indian culture, and to make information available to
tribes. On July 17, 2017, as part of our status review process, we sent
out notification letters to 11 Tribes that are in proximity to the
known historical range of the Franklin's bumble bee (6 Tribes in Oregon
and 5 Tribes in California). The letter provided the Tribes early
notification that were conducting a status review for Franklin's bumble
bee and solicited their input to ensure that we had the best scientific
data available to inform our subsequent finding on the status. We did
not receive a response from any of the Tribes.
References Cited
A complete list of references cited in this rule is available on
the internet at https://www.regulations.gov under Docket No. FWS-R1-ES-
2018-0044 and upon request from the Oregon Fish and Wildlife Office
(see FOR FURTHER INFORMATION CONTACT).
Authors
The primary authors of this rule are the staff members of the Fish
and Wildlife Service's Species Assessment Team and the Oregon Fish and
Wildlife Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species, Exports, Imports, Reporting and
recordkeeping requirements, Transportation.
Regulation Promulgation
Accordingly, we amend part 17, subchapter B of chapter I, title 50
of the Code of Federal Regulations, as set forth below:
PART 17--ENDANGERED AND THREATENED WILDLIFE AND PLANTS
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 1531-1544; and 4201-4245, unless
otherwise noted.
0
2. Amend Sec. 17.11 in paragraph (h) by adding an entry for ``Bee,
bumble, Franklin's'' to the List of Endangered and Threatened Wildlife
in alphabetical order under INSECTS to read as follows:
Sec. 17.11 Endangered and threatened wildlife.
* * * * *
(h) * * *
----------------------------------------------------------------------------------------------------------------
Listing citations and
Common name Scientific name Where listed Status applicable rules
----------------------------------------------------------------------------------------------------------------
* * * * * * *
Insects
Bee, bumble, Franklin's......... Bombus franklini.. Wherever found.... E............ 85 FR [Insert Federal
Register page where
the document begins],
8/24/21.
* * * * * * *
----------------------------------------------------------------------------------------------------------------
Martha Williams,
Principal Deputy Director, Exercising the Delegated Authority of the
Director, U.S. Fish and Wildlife Service.
[FR Doc. 2021-17832 Filed 8-23-21; 8:45 am]
BILLING CODE 4333-15-P