Endangered and Threatened Wildlife and Plants; Determination of Endangered Status for Arctostaphylos franciscana, 54434-54450 [2012-21742]
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within 2 degrees of the geostationarysatellite orbit, taking into account
atmospheric refraction. However,
exception may be made in unusual
circumstances upon a showing that
there is no reasonable alternative to the
transmission path proposed. If there is
no evidence that such exception would
cause possible harmful interference to
an authorized satellite system, said
transmission path may be authorized on
waiver basis where the maximum value
of the equivalent isotropically radiated
power (EIRP) does not exceed:
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(c) 12.7 to 13.25 GHz. No directional
transmitting antenna utilized by a fixed
station operating in this band with EIRP
greater than 45 dBW may be aimed
within 1.5 degrees of the geostationarysatellite orbit, taking into account
atmospheric refraction.
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■ 7. Amend § 101.147 by revising
paragraph (i) introductory text, adding
paragraph (i)(9), revising paragraph (o)
introductory text, and adding paragraph
(o)(8) to read as follows:
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[FR Doc. 2012–21335 Filed 9–4–12; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS–R8–ES–2010–0049;
4500030113]
RIN 1018–AX89
Endangered and Threatened Wildlife
and Plants; Determination of
Endangered Status for Arctostaphylos
franciscana (Franciscan manzanita)
Throughout Its Range
Fish and Wildlife Service,
Interior.
ACTION: Final rule.
AGENCY:
We, the U.S. Fish and
Wildlife Service (Service), determine
that Arctostaphylos franciscana
(Franciscan manzanita) meets the
definition of an endangered species
under the Endangered Species Act of
§ 101.147 Frequency assignments.
1973, as amended (Act). This final rule
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implements the Federal protections
(i) 5,925 to 6,425 MHz. 60 MHz
provided by the Act for this species. We
authorized bandwidth.
are simultaneously publishing a
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proposed rule to designate critical
1
(9) 60 MHz bandwidth channels:
habitat for Arctostaphylos franciscana
in a separate Federal Register notice.
Receive
DATES: This rule becomes effective
Transmit (receive) (MHz)
(transmit)
(MHz)
October 5, 2012.
ADDRESSES: This final rule is available
5964.97 .....................................
6217.01
6024.27 .....................................
6276.31 on the Internet at https://
6083.57 .....................................
6335.61 www.regulations.gov and at the
6142.87 .....................................
6394.91 Sacramento Fish and Wildlife Office.
Comments and materials received, as
1 The highest available channel should be
well as supporting documentation used
selected, except where such a choice would
impede the efficiency of local frequency co- in the preparation of this rule, will be
available for public inspection, by
ordination efforts.
appointment, during normal business
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hours at: U.S. Fish and Wildlife Service,
(o) 10,700 to 11,700 MHz. 80 MHz
Sacramento Fish and Wildlife Office,
authorized bandwidth.
2800 Cottage, Room W–2605,
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Sacramento, CA 95825; 916–414–6600
1
(8) 80 MHz bandwidth channels:
(telephone); 916–414–6712 (facsimile).
FOR FURTHER INFORMATION CONTACT:
Susan Moore, Field Supervisor,
Sacramento Fish and Wildlife Office
Receive
Transmit (receive) (MHz)
(transmit)
(see ADDRESSES section). If you use a
(MHz)
telecommunications device for the deaf
(TDD), call the Federal Information
10745 ........................................
11235
Relay Service (FIRS) at 800–877–8339.
10825 ........................................
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SUPPLEMENTARY INFORMATION:
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SUMMARY:
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Executive Summary
Why we need to publish a rule. This
is a final rule to list Arctostaphylos
1 The highest available channel should normally be selected, except where such a choice franciscana as an endangered species
would impede the efficiency of local frequency under the Endangered Species Act.
coordination efforts.
Under the Act, if a species is
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determined to be an endangered or
threatened species we are required to
promptly publish in the Federal
Register and make a determination on
our proposal within one year. We were
petitioned in 2010 to list A. franciscana
as an endangered or threatened species.
We determined in our 12-month finding
that listing was warranted, and we
proposed to list the species as an
endangered species in September 2001.
This final rule constitutes our final
determination for this species as
required by the Act.
The basis for our action. Under the
Endangered Species Act, we are
required to determine whether a species
is endangered or threatened 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. We
reviewed all available scientific and
commercial information pertaining to
these factors in our status review of the
species and determined that the species
was limited to one plant remaining in
the wild. We proposed that the species
was endangered due to threats in the
five factors, as follows. The primary
threat to Arctostaphylos franciscana is
from the present or threatened
destruction, modification, or
curtailment of the species’ habitat or
range. All original occupied habitat of
the species has been lost, and its current
range has been reduced to a single
location that supports a single A.
franciscana plant. Furthermore, limited
suitable habitat remains available to
support a viable population of the
species. The remaining plant is
vulnerable to overcollection or damage
if visitors harvest cuttings or seeds.
Sudden oak death, which is caused by
the pathogen Phytophthora cinnamomi,
and infections caused by other
Phytophthora species are serious threats
to Arctostaphylos franciscana because
only one plant occurs in the wild and
the diseases are easily spread. Predation
is an ongoing but lesser threat.
Additional threats include climate
change, altered fire regime, soil
compaction from visitor use, vandalism,
loss of genetic diversity, loss of
pollinators, stochastic events, effects of
small population size, and
hybridization. In the proposed rule, we
considered these threats to be
significant and ongoing, but we did not
find that we had sufficient information
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to determine critical habitat at the time.
In this final rule, we utilize public
comments and peer review to inform
our final determination, as required
under the Act.
Peer review and public comments. In
this final rule, we present and respond
to peer reviewer and public comments.
We obtained peer reviews from
knowledgeable individuals with the
scientific expertise to review our
technical assumptions, analysis,
adherence to regulations, and whether
or not we had used the best available
information. These peer reviewers
generally concurred with our methods
and conclusions, and they provided
additional information, clarifications,
and suggestions to improve this final
rule. In particular, peer reviewers
provided information on the physical
and biological features required by the
species, and on locations of remnant
natural habitat that retained these
features, suggesting that proposal of
critical habitat would be determinable
and prudent. Accordingly, a proposed
rule to designate critical habitat is being
published concurrently with this final
rule to list the species as endangered.
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Background
It is our intent to discuss only those
topics directly relevant to the listing of
Arctostaphylos franciscana under the
Act (16 U.S.C. 1531 et seq.) in this final
rule. For further information on the
species’ biology and habitat, population
abundance and trend, distribution,
demographic features, habitat use and
conditions, threats, and conservation
measures, please see the September 8,
2011, proposed listing for the species
(76 FR 55623) published in the Federal
Register, or the Recovery Plan for
Coastal Plants of the Northern San
Francisco Peninsula (Service 2003).
These documents are available from the
Environmental Conservation Online
System (ECOS) (https://ecos.fws.gov/
ecos), the Sacramento Fish and Wildlife
Office Web site (https://www.fws.gov/
sacramento/), or from the Federal
eRulemaking Portal (https://
www.regulations.gov).
Prudency Determination
In our proposed listing rule for
Arctostaphylos franciscana (76 FR
55623; September 8, 2011), we stated
that we believed that critical habitat was
not determinable at the time of the
proposal due to a lack of knowledge of
what physical or biological features
were essential to the conservation of the
species, or what other areas outside the
site that is currently occupied may be
essential for the conservation of the
species. Subsequently, we requested
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In the wild, Arctostaphylos
franciscana is an obligate-seeding
species (it reproduces primarily from
seed rather than from burls) (Vasey
2010, p. 1). Arctostaphylos (manzanita)
species are members of the chaparral
plant community, which have a variety
of triggers for seed germination
including heat, smoke, and light (Keeley
1987, p. 434). Arctostaphylos species
have germinated after being exposed to
charate (ground charred wood) (Keeley
1987, pp. 435, 440), which suggests that
fire or conditions that simulate fire
stimulate germination of the seeds.
Based on work with other species of
Arctostaphylos, the establishment of
successful populations of A. franciscana
may require the presence of a pollinator
community (primarily bumblebees
(Bombus spp.) but also other insects), a
fruit dispersal community (primarily
rodents), and a mutually beneficial soil
mycorrhizal fungi community (see
Historical Distribution and Habitat
below) (Parker 2011, p. 1). The seeds of
Arctostaphylos are dispersed primarily
by rodents that consume the fruits, but
Species Information
also by other mammals, including
Arctostaphylos franciscana is a low,
coyotes (Canis latrans) and foxes (T.
spreading-to-ascending, evergreen shrub Parker 2011, pers. comm.; Vasey 2011a,
in the heath family (Ericaceae) that may p. 1). Seed-eating animals such as
reach 0.6 to 0.9 meters (m) (2 to 3 feet
coyotes, gray foxes (Urocyon
(ft)) in height when mature (Chasse et al. cinereoargenteus), red foxes (Vulpes
2009, p. 5). Its leaves are about 1.5 to 2
vulpes), raccoons (Procyon lotor),
centimeters (cm) (0.6 to 0.8 inches (in))
California quail (Callipepla californica),
long, are isofacial (have the same type
and rodents such as the California vole
of surface on both sides), and are
(Microtus californicus) are known to
oblanceolate (longer than they are wide
occur on the Presidio of San Francisco
and wider towards the tip) (Eastwood
(Presidio), a unit of the National Park
1905, p. 201; Chasse et al. 2009, p. 39).
System, on the San Francisco peninsula
Its mahogany brown fruits are about 6
where A. franciscana is found (National
to 8 millimeters (mm) (0.24 to 0.32 in)
Park Service (NPS) 2012). Animals such
wide, while its urn-shaped flowers
as coyotes and foxes eat the
measure about 5 to 7 mm (0.2 to 0.28
Arctostaphylos fruit and may travel long
in) long (Wallace 1993, p. 552; Service
distances before depositing their scat.
2003, p. 57).
Any undigested fruit left in the scat can
A closely related species,
then be harvested by rodents and either
Arctostaphylos hookeri ssp. ravenii
eaten or buried. Parker (2010b, p. 1)
(Presidio or Raven’s manzanita), which
found that 70 percent of the fruits
was federally listed as endangered on
buried by rodents were located deeper
October 26, 1979 (44 FR 61909), looks
than 2 cm (0.78 in), which is the
similar but has a growth habit that is
maximum soil depth at which seeds are
more prostrate, leaves that are more
typically killed by wildfire. Seed has
rounded, fruits that are smaller and less been removed from the wild plant, and,
red in color, and flowers that are smaller although it has not been directly
and more spherical (Service 2003, pp.
observed, California voles have been
55, 57). Arctostaphylos hookeri ssp.
trapped near the wild plant and are
ravenii has recently undergone a
likely responsible for the seed
taxonomic revision to A. montana ssp.
harvesting (Carlen 2012, p. 1; Estelle
ravenii, and we will be referring to the
2012d, p. 1).
listed species by this name throughout
Listed Entity Analysis
this rule (see Genetics and Taxonomy
The Arctostaphylos franciscana
section below). Another somewhat
similar appearing species, though not as plants that exist in cultivation fall into
three categories: (1) Cuttings and rooted
closely related, is A. uva-ursi
(bearberry), which can be distinguished specimens collected from the Laurel
Hill Cemetery and transplanted to
by its lack of isofacial leaves (Chasse et
various managed botanical gardens in
al. 2009, p. 39).
information from the public during the
public comment period and solicited
information from peer reviewers on
whether the determination of critical
habitat was prudent and determinable.
We also asked for information about the
physical or biological features that are
essential to the conservation of the
species and what areas contained those
features or were otherwise essential for
the conservation of the species. Based
on the information we received on the
physical or biological features for A.
franciscana, and information on areas
otherwise essential for the species, we
have determined that the designation of
critical habitat is prudent and
determinable. We are therefore
proposing critical habitat elsewhere in
today’s Federal Register. For more
information regarding our determination
to designate critical habitat please see
our response to comments below and
the proposed rule to designate critical
habitat for A. franciscana published in
the Proposed Rules section of today’s
Federal Register.
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San Francisco, Berkeley, and Claremont
prior to 1947; (2) specimens currently
propagated in greenhouses from cuttings
and layers taken from the wild plant in
2010; and (3) specimens, some of which
may be of unknown origin, sold in the
nursery trade or transplanted into home
gardens. We consider the single wild
plant and plants identified in (1) and (2)
above to be the listed entity under the
Act. Our rationale for not including
plants identified in item (3) above is
outlined below.
The Arctostaphylos franciscana
plants found in botanical gardens may
represent from one to six genetically
distinct plants other than the single
wild plant (Chasse et al. 2009, p. 7;
Chasse 2011a, p. 1; Chasse 2011b, p. 1;
Vasey 2011b, pp. 2, 3), and cuttings
from those plants may contribute
genetic material to efforts to expand the
number of wild plants. The botanical
garden plants are not considered part of
the wild population and, therefore, are
not considered in the assessment of
species status, although they will be
considered to be listed when this final
rule becomes effective (see the DATES
section above). The cuttings and layers
collected from the wild plant currently
propagated in greenhouses are being
considered in the assessment of the
species’ status. These cuttings from the
wild plant will be planted with A.
franciscana specimens propagated in
botanical gardens to establish additional
populations of the species. We have
concluded that the third category of
plants, those cultivated for private or
commercial uses, will not aid in the
conservation or recovery of the species
in the wild because some cultivated
plants may be hybrids and bred for
landscape use and thus offer minimal
contribution to conservation.
Current Distribution
In October 2009, an ecologist
identified a plant growing in a concretebound median strip along Doyle Drive
in the Presidio as Arctostaphylos
franciscana (Chasse et al. 2009, pp. 3, 4;
Gluesenkamp 2010, p. 7). The plant’s
location was directly in the footprint of
a roadway improvement project
designed to upgrade the seismic and
structural integrity of the south access to
the Golden Gate Bridge (California
Department of Transportation (Caltrans)
et al. 2009, p. 1; Chasse et al. 2009, p.
10).
Several agencies, including the
Service, established a Memorandum of
Agreement (MOA) and conservation
plan for the species (see Previous
Federal Actions section below) (Caltrans
et al. 2009). The conservation partners
concluded that leaving the plant
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undisturbed at its original site would
compromise public safety and cultural
resources by the potential curtailment or
redesign of the roadway improvement
project (Chasse et al. 2009, pp. 9, 10).
The conservation plan evaluated
potential translocation sites, established
procedures for preparation of the new
site and for the translocation itself, and
called for management and monitoring
(both short- and long-term) of the
translocated plant, with the goal of
eventually establishing self-sustaining
populations of the species in the wild
(Chasse et al. 2009, pp. 23–27, 29–30).
Following recommendations in the
conservation plan, the Arctostaphylos
franciscana plant was moved
successfully to a new site within the
Presidio in January 2010. The Presidio
site was chosen after careful
consideration of its appropriate soil type
and the management and monitoring
capabilities of the NPS and the Presidio
Trust. Subsequent monitoring reports
indicate the translocated plant
continues to do well at its new location
(Yam 2010, pp. 1, 3–14; Young 2010a,
p. 1; Young 2012, p. 1).
Historical Distribution and Habitat
Known historical occurrences and
collections of Arctostaphylos
franciscana are from serpentine
maritime chaparral, a plant community
dominated by Arctostaphylos and
Ceanothus (California lilac) species, on
the San Francisco peninsula. This area
is part of a region that Willis Linn
Jepson named the Franciscan Area, one
of 10 areas he considered to have the
highest concentration of endemic plant
species in California (Jepson 1925, pp.
11–14). An endemic species is one that
is native to, and restricted to, a
particular geographical area. Native
habitats on the San Francisco peninsula
have been largely converted to urban
areas of the City of San Francisco, and
habitat that might have supported A.
franciscana is now mostly lost to
development or habitat conversion from
the introduction of nonnative plant
species (Chasse 2010, p. 2;
Gluesenkamp 2010, p. 7; Chasse 2011c,
p. 1).
Chasse (2009, pp. 6, 7) has noted that
information on the plant community
that historically included
Arctostaphylos franciscana is largely
missing from the literature. Early
records describe the species as growing
‘‘on rocky ground’’ (Eastwood 1905, p.
202), on ‘‘bare, stony bluff on Laurel
Hill Cemetary [sic]’’ (Brandegee 1908),
and with coast live oak (Quercus
agrifolia), coast blue blossom
(Ceanothus thyrsiflorus), and coyote
brush (Baccharis pilularis) (Wieslander
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1938). Arctostaphylos franciscana was
also observed ‘‘forming flat masses over
serpentine outcroppings and humusfilled gravel and flopping down over the
sides of gray and chrome rocks.
Ericameria, Baccharis, Ferns,
Buckwheats, and Golden Yarrow grow
among it; and over it stand Toyons and
Live Oaks.’’ Additionally, A. montana
ssp. ravenii was found at nearly all A.
franciscana locations. These
observations, along with the geology
and climate of historical sites, indicate
that the species’ historical community
likely consisted of a mosaic of coastal
scrub, barren serpentine maritime
chaparral, perennial grassland, and
occasional woodlands of coast live oak
and toyon shrubs and small trees
(Chasse 2009, pp. 6, 7).
Arctostaphylos franciscana is
considered to be endemic to the San
Francisco peninsula, and historically
occurred in areas with serpentine soils,
bedrock outcrops, greenstone, and
mixed Franciscan rock, typically
growing in mixed populations with A.
montana ssp. ravenii (Service 2003, pp.
95, 96; Chasse et al. 2009, p. 6). The
Doyle Drive A. franciscana site was
comprised of disturbed soil over
serpentinite (Chasse et al. 2009, p. 3).
Serpentine soil restricts the growth of
many plants due to its high nickel and
magnesium concentrations, and thus
tends to support unique plant
communities (Brooks 1987, pp. 19, 53;
Service 2003, p. 16) because relatively
few plant species can tolerate such soil
conditions. These conditions generally
result in semibarren soil and a lack of
competing plants, which benefits
serpentine-tolerant plants (Bakker 1984,
p. 79) such as A. franciscana.
The coastal upland habitat of
Arctostaphylos franciscana is
influenced by cool, humid conditions
and frequent summer fog. Summer fog
is important to upland coastal
vegetation and partly determines the
distribution of coastal species
(Johnstone and Dawson 2010, p. 4533).
Besides serpentine soil and cool air
temperatures (Parker 2010c, p. 1),
summer fog is one of the primary habitat
requirements for A. franciscana (Vasey
2010, p. 1). Summer fog results from
two phenomena upwelling of cold
coastal ocean water and temperature
inversion of hot air flowing toward the
ocean over a cool humid marine air
layer below (Johnstone and Dawson
2010, p. 4533; Vasey 2010, p. 1). Fog
reduces sunlight and air temperature,
and raises humidity. Summer fog
provides a source of water for plants,
including Arctostaphylos species, by
condensing in the plant canopy and
falling directly as water to the soil
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where it is taken up by the plant’s roots
or directly by leaves (Johnstone and
Dawson 2010, p. 4533; Vasey 2010, p.
1).
Historically, the maritime serpentine
chaparral plant community, of which
Arctostaphylos franciscana is a part,
may have been present in the
southeastern portion of the San
Francisco area (for example, Potrero Hill
and Bayview Hill), but the cumulative
effects of burning by native Americans,
grazing during the Spanish/Mexican
period, and later more grazing and
firewood gathering during the U.S.
military period may have converted the
maritime chaparral to grassland or
depauperate coastal scrub (Chasse 2010,
p. 2). Prior to 1947, A. franciscana was
known from three locations: the
Masonic and Laurel Hill Cemeteries in
San Francisco’s Richmond District, and
Mount Davidson in south-central San
Francisco (Service 2003, pp. 16, 62, 95;
Chasse et al. 2009, p. 4). Unconfirmed
sightings were also noted at a possible
fourth location near Laguna and Haight
Streets (Chasse 2012, p. 1). By 1947, the
Masonic and Laurel Hill Cemetery sites
were removed and the grounds were
destroyed in preparation for commercial
and urban development (Chasse et al.
2009, p. 7). The Mount Davidson and
Laguna and Haight Streets locations
were lost to urbanization as well. Until
October 2009, A. franciscana had not
been recorded in the wild since 1947
(Chasse et al. 2009, pp. 3, 7), although
no systematic surveys are known to
have taken place to search for potential
remaining individuals (Chasse 2010, p.
1).
Cultivated Arctostaphylos franciscana
Between 1930 and 1947, prior to the
loss of the wild plants, botanists
collected cuttings and rooted specimens
from confirmed wild Arctostaphylos
franciscana plants, possibly
representing between one and six
distinct genotypes, and propagated them
in botanical gardens (Chasse et al. 2009,
p. 7; Chasse 2011a, p. 1; Chasse 2011b,
p. 1; Service 2003, p. 96; Vasey 2011b,
p. 2). The number of distinct genotypes
depends on whether the botanical
garden specimens were started from
cuttings of the same individual (which
would mean multiple plants have
identical genotypes (genetic
constitutions)), or whether each
specimen originated from a separate
plant (in which case they would have
different genotypes) (Chasse 2011a, p. 1;
Chasse 2011b, p. 1; Vasey 2011b, pp. 2,
3).
Modern collections of this plant at
East Bay Regional Park District’s
Botanical Garden at Tilden Regional
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Park, San Francisco Botanical Garden
(formerly known as Strybing
Arboretum), Rancho Santa Ana Botanic
Garden, Claremont, and University of
California (UC) Berkeley Botanical
Garden include some of the original
specimens from Laurel Hill, as well as
specimens propagated vegetatively after
the species was thought to be extinct in
the wild (Chasse et al. 2009, pp. 6–8).
Accession records for the botanical
garden specimens indicate that some
specimens collected and planted prior
to 1947 did not survive and others are
duplicates of original collections,
leaving possibly only two specimens
confirmed to have been original plants
transplanted from Laurel Hill (Chasse
2011b, p. 1; Smisko 2012, p. 1). Further
genetic work will verify whether plants
with differing morphological features
prove to be additional Arctostaphylos
franciscana individuals. Although some
of the botanical garden specimens may
have different genotypes, which is
generally the result of sexual
reproduction (sprouting from seed)
rather than clonal reproduction
(vegetative reproduction from cuttings
or plant parts other than seeds), all of
the botanical garden specimens are
considered to be A. franciscana until
further genetic work can be conducted.
The number of existing distinct
genotypes cannot currently be
determined because a suitable genetic
sampling technique has not yet been
developed (Chasse 2011a, p. 1).
Under the conservation plan for the
relocated wild plant, cuttings and
rooted specimens from the wild plant
are also being cultivated. Cuttings from
the plant, both nonrooted stems and
layering stems (stems that have rooted at
their leaf nodes), were taken for
vegetative propagation prior to
translocation of the Arctostaphylos
franciscana plant in January 2010
(Chasse et al. 2009, pp. 10–16, 40–42,
Young 2010a, p. 1). This material was
distributed to seven locations, including
UC Berkeley Botanic Garden, Regional
Parks Botanic Garden, UC Santa Cruz
Botanical Garden, San Francisco
Botanical Garden, Cal Flora Nursery,
Presidio Nursery, and the Presidio Trust
Forester (Young 2011, p. 1 of attachment
2). As of February 2012, 351 clones
continue to survive at these locations
(Young 2012, p. 1). A total of 1,346 A.
franciscana seeds were collected from
the plant in 2009, before it was
transplanted; an estimated 2,100 seeds
were collected in July and August 2010;
and 19 seeds were collected in 2011
(Frey 2010, p. 1; Young 2010a, p. 1;
Young 2012, p. 1). The numbers of seeds
collected are estimates based on weight
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54437
of seed collected (Laskowski 2012, p. 1).
No attempts have yet been made to
germinate A. franciscana seeds (Young
2012, p. 1). Two rooted A. franciscana
cuttings were outplanted to managed
sites at the UC Santa Cruz Arboretum in
January 2011 (Kriegar 2011,
unpaginated). The conservation plan
calls for eventual propagation of seeds
(including any seeds collected from the
soil around the plant’s original
location), and for genetic testing of
resulting plants. Seeds fertilized in the
wild could result from cross-pollination
from another individual Arctostaphylos
franciscana or a closely related species
to produce a genetically unique
individual (Chasse et al. 2009, p. 13).
Additionally, because the roots of most
Arctostaphylos individuals establish a
mutually beneficial association with
mycorrhizal fungi in the soil, the
conservation plan establishes means by
which the soil for propagating cuttings
and seeds should be inoculated with
spores from such fungi (Chasse et al.
2009, p. 9). Propagation of A.
franciscana seed and inoculation of
seeds and cuttings by mycorrhizal fungi
have not yet occurred. Soil surrounding
the wild plant has been examined for
presence of a seedbank, but no A.
franciscana seeds have been found
(Young 2011, p. 1; Young 2012, p. 1).
Genetics and Taxonomy
At one time Arctostaphylos
franciscana and A. montana ssp. ravenii
were considered to be subspecies of A.
hookeri (Hooker’s manzanita). However,
recent taxonomic revisions have
established A. montana ssp. ravenii and
A. franciscana as separate species.
These revisions have been based
primarily on genetic comparisons,
including the fact that A. franciscana is
diploid while A. montana ssp. ravenii is
tetraploid (having four sets of
chromosomes, 26 chromosome pairs)
(Service 2003, p. 95; Parker et al. 2007,
pp. 149, 150; Chasse et al. 2009, p. 6).
The identification of the wild plant as
A. franciscana has since been confirmed
with 95 percent confidence based on
morphological characteristics (Chasse et
al. 2009, pp. 3, 4; Vasey and Parker
2010, pp. 1, 5). Additional tests indicate
that the plant is diploid, consistent with
A. franciscana (Vasey and Parker 2010,
p. 6). Molecular genetic data also
indicate that the plant is A. franciscana
(Parker 2010a). Based on the best
available scientific information, we
consider the individual found along
Doyle Drive in October 2009 to be A.
franciscana (Vasey and Parker 2010, pp.
1, 5–7).
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Previous Federal Actions
Arctostaphylos franciscana was
originally proposed for listing as an
endangered species under the Act in
1976 (41 FR 24524; June 16, 1976). In
1980, it was included in the list of
Category 1 candidates for listing as one
of the taxa retaining a high priority for
addition to the list, subject to
confirmation of extant wild populations.
At that time, the species was thought to
be extinct in the wild, although it was
known to be extant in cultivation (45 FR
82479; December 15, 1980). It was
included as a species of concern in the
Recovery Plan for Coastal Plants of the
Northern San Francisco Peninsula
(Service 2003, pp. 95–96).
On December 23, 2009, we received a
petition dated December 14, 2009, from
Wild Equity Institute, Center for
Biological Diversity, and California
Native Plant Society requesting that
Arctostaphylos franciscana be listed as
endangered on an emergency basis
under the Act and that critical habitat be
designated. Included in the petition was
supporting information regarding the
species’ taxonomy and ecology,
historical and current distribution,
present status, and actual and potential
causes of decline. On January 26, 2010,
we acknowledged the receipt of the
petition in a letter to Wild Equity
Institute. In that letter, we responded
that we had reviewed the information
presented in the petition and
determined that issuing an emergency
rule to temporarily list the species,
under section 4(b)(7) of the Act, was not
warranted. Our rationale for this
determination was that, although only a
single plant of this species remained in
the wild, the individual had recently
been transplanted to a new location on
Federal land. Additionally, a
conservation plan (Chasse et al. 2009,
pp. 1–44) and associated MOA (cited
herein as Caltrans et al. 2009) signed by
five Federal and State wildlife and land
management agencies (conservation
partners) successfully addressed the
concerns raised by the petition to the
extent that none of those concerns
constituted an ‘‘emergency posing a
significant risk to the well-being of the
species’’ (50 CFR 424.20(a)). The
Federal agencies participating in the
MOA are the NPS and the Service. The
State of California is represented by
Caltrans and the California Department
of Fish and Game (CDFG). The Presidio
Trust, a wholly owned government
corporation that jointly manages the
Presidio with NPS, also participates (71
FR 10608; March 2, 2006).
The transplanted plant is considered
to be the single remaining plant in the
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wild, despite having been transplanted
to the Presidio. The original habitat of
the plant was threatened by the ongoing
redevelopment of Doyle Drive, but that
threat was removed by moving the plant
to a new location (translocation).
Potential immediate threats in the new
location, including the danger that the
plant might not survive the move and
transplantation, were addressed by
provisions in the conservation plan for
collecting and propagating rooted
clones, seeds, and cuttings from the
original plant prior to translocation. The
conservation plan provides for the longterm propagation, and eventual
reestablishment in wild populations, of
all remaining genetic lines, including
those from the surviving wild plant and
from the individuals located in two
botanical gardens, which were collected
from historically confirmed locations. It
also includes long-term monitoring
provisions. While these provisions do
not remove the need for further review
of the species’ status, they appear to be
effective for protecting the species in the
short term.
We published a 90-day finding in the
Federal Register on August 10, 2010 (75
FR 48294), in which we found that the
petition presented substantial scientific
or commercial information indicating
that listing this species may be
warranted. On June 14, 2011, Wild
Equity Institute filed a complaint that
alleged that, given our 90-day finding,
the Service had failed to make the
required 12-month finding on the
petition in a timely manner. On
September 8, 2011, we published a
combined 12-month finding and
proposed rule in the Federal Register in
which we determined that listing
Arctostaphylos franciscana was
warranted, and, as a result, we proposed
to list the species as endangered (76 FR
55623). We also stated that we did not
find critical habitat to be determinable
at that time, and requested information
and comments on whether designation
of critical habitat for the species was
prudent and determinable.
The Presidio is under joint
management by the Golden Gate
National Recreation Area (GGNRA), a
part of NPS, and the Presidio Trust. The
wild Arctostaphylos franciscana plant is
located in the portion of the Presidio
managed by the Presidio Trust. The
plant is considered to be wild because
it has been moved to an undeveloped
area of the Presidio that is managed as
natural habitat. Although the plant is
currently receiving care (monitoring and
insect removal) associated with its
transplantation and recent infestation by
insects, it is not receiving the level of
protection, water, or nutrients given to
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the plants in botanical gardens or to
those within the nursery trade.
Summary of Comments and
Recommendations
In the proposed rule published on
September 8, 2011 (76 FR 55623), we
requested that all interested parties
submit written comments on the
proposal by November 7, 2011. We also
contacted appropriate Federal and State
agencies, scientific experts and
organizations, and other interested
parties and invited them to comment on
the proposal. A newspaper notice
inviting general public comment for a
period of 15 days was published in the
San Francisco Chronicle on June 5,
2012. A question and answer sheet and
news release regarding the species was
posted online on our Web site for the
public. We did not receive any requests
for a public hearing.
During the comment periods for the
proposed rule, we received eight
comment letters directly addressing the
proposed listing of Arctostaphylos
franciscana as endangered. All public
commenters supported listing the
species as endangered. Three
commenters supported designation of
critical habitat and provided opinions
on the value of critical habitat
designation and the threats resulting
from lack of this designation. One
commenter opposed critical habitat
designation. All substantive information
provided during the comment periods
has either been incorporated directly
into this final determination or is
addressed below.
Peer Review
In accordance with our peer review
policy published on July 1, 1994 (59 FR
34270), we solicited expert opinion
from five knowledgeable individuals
with scientific expertise that included
familiarity with Arctostaphylos
franciscana and its habitat, biological
needs, and threats. We received
responses from four of the peer
reviewers.
We reviewed all comments received
from the peer reviewers for substantive
issues and new information regarding
the listing and critical habitat of
Arctostaphylos franciscana. The peer
reviewers generally concurred with our
methods and conclusions regarding
listing and provided additional
information, clarifications, and
suggestions to improve the final rule;
however, three reviewers disagreed with
our comments that designation of
critical habitat was not prudent or
determinable, and they provided
supporting information regarding
critical habitat. The fourth peer reviewer
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indicated that publicizing the location
of the transplanted plant could increase
the threat of infection by Phytophthora
species. Additionally, this peer reviewer
noted that the threat to A. franciscana
was greater than stated in the proposed
rule due to the presence of other species
of Phytophthora in the San Francisco
Bay area. Peer reviewer comments are
addressed in the following summary
and incorporated into the final listing
rule as appropriate. A proposed rule to
designate critical habitat for A.
franciscana is published in the
Proposed Rules section of today’s
Federal Register. Please see that
proposed rule for information on
submitting a comment on our proposed
designation of critical habitat for A.
franciscana.
Peer Reviewer Comments
(1) Comment: All peer reviewers
provided comments on conservation
measures, recommendations for
outplanting cuttings and selection of
planting sites, and additional
information on threats to the species
from the five factors discussed below in
Summary of Factors Affecting the
Species.
Our Response: Recommendations
regarding outplanting and selection of
planting sites have been reviewed for
the proposed critical habitat and will be
considered during the development of a
recovery plan. All other appropriate
information was incorporated into this
final rule.
(2) Comment: Three peer reviewers
and three public commenters stated that
designation of critical habitat is prudent
and determinable.
Our Response: Critical habitat is
defined in section 3 of the Act as: (1)
The specific areas within the
geographical area occupied by the
species, at the time it is listed in
accordance with the Act, on which are
found those physical or biological
features that are essential to the
conservation of the species, and which
may require special management
considerations or protection; and (2)
specific areas outside the geographical
area occupied by the species at the time
it is listed, upon a determination that
such areas are essential for the
conservation of the species. The peer
reviewers provided information on the
ecological requirements of
Arctostaphylos franciscana and areas
with the highest potential for
establishing new populations. Based on
this information, we have determined
that the designation of critical habitat is
prudent and determinable. All known
remaining historic locations as well as
the site of the transplanted wild plant
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have been evaluated, and the areas that
have met our criteria to be included as
proposed critical habitat have been
identified. We are proposing to
designate critical habitat for the species
concurrently with this final rule. That
proposal is published in the Proposed
Rules section of today’s Federal
Register. Please see that proposed rule
for information on submitting a
comment on our proposed designation
of critical habitat for A. franciscana.
(3) Comment: Two peer reviewers
disagreed with our statement that small
sites on the order of 0.4 hectare (ha) (1
acre (ac)) may not be suitable for
Arctostaphylos franciscana. One peer
reviewer stated that while small sites
may facilitate the growth of nonnative
plant species, A. franciscana would be
started from cuttings, not from seed, and
management efforts could easily
accommodate competition from
nonnative plants, as established woody
species are not easily displaced by
weeds. The second peer reviewer noted
that there are many natural occurrences
of rare Arctostaphylos species existing
in small, isolated remnants of habitat
where soils and climate are suitable.
Our Response: Some invasive plant
species in the Presidio and in other San
Francisco peninsula areas have been
shown to be difficult to control. For
example, on Mount Davidson, which
previously supported a population of
Arctostaphylos franciscana, invasive
plant species, including Eucalyptus
spp., invasive ivy, and other species,
have largely displaced native vegetation
on portions of the site. We agree that
some rare species of Arctostaphylos
have persisted on small parcels of
suitable habitat; however, in order to
maximize the potential of establishing
multiple, successful populations of A.
franciscana, selection of suitable sites
that require the least amount of longterm maintenance and promise the
greatest opportunity for growth is
necessary. However, we will evaluate
small sites during our process to
designate critical habitat for the species.
(4) Comment: Two peer reviewers
questioned our statement under Factor
A in the proposed rule that small,
isolated areas of habitat can be drier
than larger ones due to evaporation and
lack of surrounding vegetation. One
reviewer stated that this does not apply
to small urban or near-urban sites
because hard surfaces such as asphalt
and cement provide additional runoff
and available moisture in these areas.
Our Response: Many of the remnant
parcels of potential habitat on the
peninsula are isolated and surrounded
by urban development or nonnative
landscaping rather than native
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54439
vegetation. One of the general effects of
this abrupt transition from natural
habitat to urban landscape or hard
surfaces is a change in the abundance
and distribution of species in the
natural habitat due to physical
conditions near the edge (the edge
effect). These conditions include
desiccation and changes in wind and
light. We agree with one peer reviewer’s
premise that hard surfaces such as
rooftops, streets, and parking lots
increase urban runoff; however, our
understanding is that when rain or
irrigation water falls on urban hard
surfaces, it flows predominately into
storm water control systems, including
gutters and storm drains, and is carried
away from urban areas rather than being
absorbed into the soil and providing
more moisture to plants.
(5) Comment: We stated under Factor
A that remaining areas of greenstone
and serpentine habitat on the peninsula
are frequently 0.4 ha (1 ac) or less in
size and may no longer be appropriate
sites for re-establishment of
Arctostaphylos franciscana due to
fragmentation and loss of native plant
diversity in the small remnant areas.
One peer reviewer pointed out the loss
of native diversity in existing stands of
vegetation is not a relevant argument
because new populations of A.
franciscana would be newly created in
the small sites.
Our Response: We appreciate the
reviewer’s point and agree that if small
remnant habitat areas were to support
Arctostaphylos franciscana, it would be
through restoration with newly
assembled populations of the species,
which could permit establishment of
other naturally co-occurring natives.
However, we remain concerned that
small sites may insufficiently support
the pollinator, fruit-dispersal, and
mycorrhizal communities that are
thought to contribute to successful
establishment of the species. We will be
looking at all potential sites when
selecting locations for outplanting.
(6) Comment: One peer reviewer
noted that the threat to Arctostaphylos
franciscana from nonnative, root-rotting
Phytophthora species is greater than
noted under Factor C in the proposed
rule. He noted that species of
Phytophthora differ in their ecological
requirements, such as optimum
temperature range. Several species of
Phytophthora have become established
in a variety of San Francisco Bay area
microclimates and could be introduced
to the vicinity of A. franciscana. He also
noted that other factors discussed under
Factor E, including climate change, soil
compaction, and low genetic diversity,
have the potential to increase the risk to
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the existing wild plant from P.
cinnamomi and other Phytophthora
species.
Our Response: This information has
been incorporated into this final rule.
Please see Factor C discussion on
threats to Arctostaphylos franciscana
associated with disease below.
(7) Comment: One peer reviewer
noted that the general strategy to recover
Arctostaphylos franciscana should be
two-fold: (A) Identify other genotypes of
A. franciscana that have been cultivated
in botanical gardens and use their
cuttings to propagate large numbers of
plants for future outplantings in
restored habitats, and (B) identify and
secure sites for outplanting these clones
and create as many populations within
the historical range as feasible.
Our Response: This information has
been incorporated into this final rule
where appropriate and will be
considered during development of the
proposed critical habitat and recovery
actions for the species.
(8) Comment: One peer reviewer
noted that the potential risks of failure
of small, restored populations are
outweighed by benefits of having a large
number of isolated populations within
the range of Arctostaphylos franciscana.
These populations would buffer the
wild A. franciscana from the threats
noted in this rule, including disease,
disturbance, predation, and climate
change. The peer reviewer further noted
that having many scattered populations
will optimize the potential for at least
some populations to adjust to climate
change.
Our Response: We concur with this
opinion and are considering this during
our development of proposed critical
habitat and recovery actions for the
species.
Comments from States
Section 4(i) of the Act states, ‘‘the
Secretary shall submit to the State
agency a written justification for his
failure to adopt regulations consistent
with the agency’s comments or
petition.’’ No comments were received
from the State regarding the proposal to
list Arctostaphylos franciscana as an
endangered species.
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Federal Agency Comments
No comments were received from any
Federal agencies.
Public Comments
(9) Comment: All seven commenters
noted that the species should be listed
and protected in the wild because only
one plant is known to exist.
Our Response: Comments noted.
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(10) Comment: One commenter noted
that not all nursery stock of
Arctostaphylos franciscana is of
unknown origin. The commenter stated
that UC Berkeley Arboretum and Yerba
Buena Nursery sell plants of known
origin. Plants from Yerba Buena Nursery
have been planted in Golden Gate Park
Arboretum, which validates their
legitimacy. The commenter further
stated that specimens from verified
sources are a vital repository and should
not be disregarded.
Our Response: The UC Berkeley
Botanical Garden does not sell
Arctostaphylos franciscana plants;
however, their stock was originally from
the Laurel Hill Cemetery and may have
been the source for plants sold by
California Native Plant Society (Forbes
2012, p. 1). We agree that some A.
franciscana plants in the nursery trade
originated from plants salvaged from the
Laurel Hill Cemetery prior to its
destruction in 1947; however, it is
difficult to trace the lineage of all
nursery plants in the intervening 65
years. Some currently available,
nursery-grown A. franciscana plants
could be cultivars selected for specific
growth characteristics, and others could
be the product of hybrid seed. Plants
from Yerba Buena Nursery that were
planted at Golden Gate Park Arboretum,
now known as the San Francisco
Botanic Garden, are believed to be A.
franciscana (D. Mahoney 2012, pers.
comm.). We encourage the use of plants
that are proven to be A. franciscana to
generate stock for additional
populations of A. franciscana. However,
introgression (the spread of genes of one
species into the gene pool of another by
hybridization) could occur if hybrid
nursery stock is outplanted near the
wild plant and cross-fertilization occurs.
Because of the uncertainty of the origin
or subsequent hybridization, we
currently only consider the plants of
confirmed origin at East Bay Regional
Parks Botanic Garden at Tilden Regional
Park and at UC Botanical Garden at
Berkeley, and the wild plant on the
Presidio to be A. franciscana and the
listed entity.
(11) Comment: One commenter noted
that there is no apparent incentive for
anyone to poach or vandalize plants in
natural settings that are available in the
nursery trade.
Our Response: Plants have been
vandalized in Golden Gate Park,
including species that are also available
in nurseries such as elm and sycamore
trees, and rose bushes (King 2010,
unpaginated; Gordon 2010,
unpaginated). The fact that a plant is
available in the nursery trade does not
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protect it from being vandalized or
poached.
(12) Comment: A commenter noted
that leaving the nursery trade specimens
of Arctostaphylos franciscana unlisted
may result in introgression. The
commenter suggests that including
nursery stock in the listed entity will
help to regulate this threat.
Our Response: Arctostaphylos
franciscana has been available to the
public in the nursery trade for many
years, and introgression of this species
with other manzanitas may have already
occurred. Including A. franciscana
nursery stock as part of the listed entity
will have no effect on controlling
hybridization of these plants. Only the
removal of A. franciscana from nursery
production could minimize its
hybridization with other species of
Arctostaphylos while in the nursery
setting.
(13) Comment: A commenter noted
that if the Arctostaphylos franciscana
plants in the nursery trade are not
considered to be the listed species, they
should be protected under the similarity
of appearance provisions of the Act.
Our Response: We acknowledge that
similarity of appearance is a tool
available to us under the Act. Section
4(e) of the Act states that the Secretary
may treat any species as an endangered
species or threatened species even
though it is not listed pursuant to
section 4 of the Act if he finds that: (1)
Such species so closely resembles in
appearance, at the point in question, a
species which has been listed that
enforcement personnel would have
substantial difficulty in attempting to
differentiate between the listed and
unlisted species; (2) the effect of this
substantial difficulty is an additional
threat to an endangered or threatened
species; and (3) such treatment of an
unlisted species will substantially
facilitate the enforcement and further
the policy of the Act. It should be noted,
however, that the basic intent of section
4(e) of the Act is to prevent the
inadvertent harm to the listed species in
the wild resulting from its similarity to
a different species that is not protected
by the Act. The Arctostaphylos
franciscana plants in the nursery trade
do not need the protection of the Act,
and including them in this listing under
section 4(e) will provide no or minimal
benefit to the wild specimen or any
future outplantings of the listed entity.
Similarity of appearance protections can
be effective in situations where
collection of a species is highly
desirable (such as for insects or
butterflies) and such collection is the
primary threat or a threat of such an
extent that not including the similar
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species with the listed entity would
greatly affect the listed species’ status.
Although collection of the remaining
wild plant and any future outplantings
is a potential threat, no known
collection has occurred to date, and we
would not consider this threat to be of
such a high level as to greatly affect the
species’ status. As a result, we have
determined that treating A. franciscana
plants in the nursery trade as
endangered under section 4(e) of the Act
would not substantially facilitate
enforcement or the policy of the Act,
and the Secretary is not invoking
section 4(e) of the Act for A.
franciscana.
(14) Comment: One commenter
disagreed with information we reported,
which indicated that lands in Area B of
the Presidio, which are managed by the
Presidio Trust, could be dispersed to the
private sector and become available for
development if the Presidio Trust is not
financially self-sufficient by 2013.
Further, the commenter does not agree
that differences in the missions of the
Presidio Trust and NPS would cause
uncertainty in the future management of
the Arctostaphylos franciscana and its
habitat.
Our Response: The Presidio Trust Act
of 1996 states in section 105(b) that the
Presidio Trust must be self-sufficient
within 15 complete fiscal years of the
first meeting of the Presidio Board of
Directors, thereby requiring that the
Trust be self-sufficient by 2013 (Presidio
Trust Act, p. 9; Presidio Trust
Management Plan 2002, p. 1). Because
this timeframe extends into the future,
there is no assurance that this goal will
be met. The Presidio Trust, as stated in
the Presidio Trust Management Plan
(2002, pp. 1, 12), is directed to preserve
natural, scenic, cultural, and recreation
resources, and at the same time ensure
that the Presidio becomes financially
self-sufficient. Again, as stated in the
Presidio Trust Management Plan (2002,
pp. 1, 12), ‘‘Congress gave the Trust the
authority to lease property and generate
revenues, and required the Presidio to
be financially self-sufficient by 2013.
Once appropriations cease, the Trust
must use the park’s building assets to
fund its rehabilitation and to pay for its
ongoing operation. No other area within
the National Park System is managed in
the same way or operates under the
same financial requirement.’’ The
mission of NPS on the Presidio, as
stated in the Golden Gate National
Recreation Area Addition Act of 1992
(16 U.S.C. 460bb), while similar to the
Presidio Trust Act in protecting values
and resources, does not include the
mandate that the public lands under
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NPS authority become financially selfsufficient.
(15) Comment: One commenter stated
that there are no remaining landfill
remediation sites on the Presidio that
have the potential to impact
Arctostaphylos franciscana, and that all
waste material has been removed from
the landfill remediation site closest to
where the wild plant is located. The
commenter noted that this work was
completed without impacts to A.
franciscana and asked that we delete the
text under Factor A that refers to the
Presidio Environmental Remediation
Program.
Our Response: Remediation of the
landfill site closest to the
Arctostaphylos franciscana on the
Presidio is being completed without
apparent impact to the wild plant, and
no further remediation projects are
located within the vicinity of the plant.
Remediation of this landfill site has
been deleted as a current threat from the
Factor A discussion.
(16) Comment: A commenter noted
that under Factor E we stated that the
Arctostaphylos franciscana plant is
located near an area available for public
events and threatened by foot traffic.
The commenter stated that this area is
available one afternoon per week for
wedding ceremonies and does not
present a threat to the plant, and
requested that reference to this event
space be removed as a threat.
Our Response: As stated in the
proposed rule, the Presidio is a highly
popular, easily accessible National Park
contiguous with the City of San
Francisco, which receives 5 million
visitors each year. The public area
described in the proposed rule, which is
available for public events, provides
views of the San Francisco Bay and the
City of San Francisco, and attracts a
large number of visitors year round. The
best information available to us
indicates that the public has
unrestricted access to this area 24 hours
a day, every day of the year; therefore,
this site may be a different location than
that referred to by the commenter.
Additionally, the Arctostaphylos
franciscana plant has been located near
common-use trails with unrestricted
access. Because of its proximity to these
heavily used areas, the plant could be
damaged accidentally or intentionally
by park users. The Presidio Trust and
NPS are concerned that authorized and
unauthorized group tours by plant
enthusiasts could overwhelm the plant
and compact the soil (T. Thomas, pers.
comm., 2011).
(17) Comment: One public commenter
stated that designation of critical habitat
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is not prudent or determinable for the
reasons stated in the proposed rule.
Our Response: As noted in our
response to comment 2, the peer
reviewers provided information on the
ecological requirements of
Arctostaphylos franciscana and areas
with the highest potential for
establishing new populations. Based on
this information, we have determined
that the designation of critical habitat is
prudent and determinable. As a result,
a proposed rule to designate critical
habitat for A. franciscana is published
in the Proposed Rules section of today’s
Federal Register. Please see that
proposed rule for information on
submitting a comment on our proposed
designation of critical habitat for A.
franciscana.
Summary of Changes From Proposed
Rule
Based on peer review and public
comments (see comments 1, 6, 7, and 15
in the Summary of Comments and
Recommendations section above), and
monitoring of the wild plant, we have
added new information in the Species
Information section and additional
threats information in the Summary of
Factors Affecting the Species section to
better characterize our knowledge of the
species’ habitat requirements and
threats. After input from peer reviewers
and public comment, we have
determined that the designation of
critical habitat is prudent and
determinable, and we are proposing to
designate critical habitat, as described
in a separate proposed critical habitat
rule in today’s Federal Register.
Summary of Factors Affecting the
Species
Section 4 of the Act and its
implementing regulations (50 CFR part
424) set forth the procedures for adding
species to the Federal Lists of
Endangered and Threatened Wildlife
and Plants. A species may be
determined to be an endangered or
threatened species due to one or more
of the five factors described in section
4(a)(1) of the Act: (A) The present or
threatened destruction, modification, or
curtailment of its habitat or range; (B)
overutilization for commercial,
recreational, scientific, or educational
purposes; (C) disease or predation; (D)
the inadequacy of existing regulatory
mechanisms; or (E) other natural or
manmade factors affecting its continued
existence. Listing actions may be
warranted based on any of the above
threat factors, singly or in combination.
Each of these factors is discussed below.
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A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
All areas of habitat originally known
to be occupied by Arctostaphylos
franciscana have been lost to urban
development or to habitat conversion
through the introduction of nonnative
plant species (Chasse et al. 2009, pp. 4,
7; Chasse 2011c, p. 1). The largest
historical occurrence was at the quarry
area of the former Laurel Hill Cemetery
in San Francisco (Chasse 2011c, p. 1).
Most of this area was converted to
residential housing and city streets after
the late 1940s. A small remaining area
of open space at Laurel Hill is
dominated by ornamental shrubs and
invasive understory plants, although
serpentine rock is visible in several
openings (Chasse 2011c, p. 1). Lawns,
pathways, and buildings, part of the
University of San Francisco campus,
now occupy the location of the Masonic
Cemetery occurrence (Chasse 2011c, p.
2). The precise location of the third
historical occurrence of A. franciscana,
at Mount Davidson, is unknown but
thought to be on one of the greenstone
outcrops (Chasse 2011c, p. 2). The
upper portions of Mount Davidson are
covered with nonnative trees and
invasive understory species; some
grassland and scrub persist on the south
and northeast sides (Chasse 2011c, p. 2).
The species’ range is now limited to the
single transplanted location on the
Presidio. In January 2010, after the
newly discovered wild plant was moved
to the Presidio, the plant’s habitat at
Doyle Drive was destroyed as part of a
Caltrans highway improvement project.
Past urban development on the San
Francisco peninsula has limited the
remaining areas of potential habitat for
Arctostaphylos franciscana by habitat
conversion and habitat degradation and,
to a lesser degree, habitat fragmentation.
Some of these small remnant areas may
no longer be suitable for reestablishment
of A. franciscana due to factors such as
dominance by other plant species
(Chasse pers. comm., 2011). Currently,
these small, isolated parcels are subject
to edge effects, such as changes in soil
moisture, changes in light, and potential
increased invasion of weed species that
would compete with A. franciscana for
limited resources (water, nutrients,
space).
Urban barriers, such as streets and
buildings, have been found to impose a
high degree of isolation on chaparral
species and, over time, to result in
decreased numbers of native plant
species and concurrent increased
numbers of nonnative plant species in
the habitat fragments (Alberts et al.
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(unpubl.) as cited in Soule et al. 1992,
p. 41; Soule et al. 1992, pp. 41–43).
These effects of urbanization on the San
Francisco peninsula are expected to
continue to affect these remnant parcels
into the future, and to pose a threat to
the establishment of additional
Arctostaphylos franciscana plants,
without assistance to restore suitable
habitat conditions and to restore plants
to suitable locations.
Additionally, nitrogen deposition may
modify habitat by increasing soil
nutrients, thus posing a current and
continuing threat to remnant habitat
that might otherwise be suitable for
Arctostaphylos franciscana. Weiss and
Luth (2003, p. 1) have conducted
research on the effects of nitrogen
deposition in a serpentine grassland
south of the San Franciscan peninsula.
They found that nitrogen deposition
from automobiles on Highway 280 (a
north-south oriented highway on the
peninsula) was responsible for higher
nitrogen levels in the soil within 400 m
(1,312 ft) on the west side and 100 m
(328 ft) on the east side of the roadway.
Nitrogen deposition was correlated with
increased nonnative grass cover in these
areas, resulting in competition for space
for native plants. Native species within
this zone are thought to be at long-term
risk from invasions of nitrogen-loving
grasses and other weedy plant species
(Weiss and Luth 2003, p. 1). An increase
in nonnative grass cover through
changed habitat conditions could
threaten the wild A. franciscana by
competing for soil moisture and
nutrients and could inhibit successful
germination of A. franciscana seed. The
entire northern San Francisco
peninsula, with the exception of the
Presidio and Golden Gate Park, has been
urbanized, and four major highways
(Highways 1, 101, 280, and 480) and
other urban roadways dissect the
peninsula. Urban areas and roadways
are a continuous source of nitrogen
deposition from automobiles, trucks,
and industrial and home heating (Weiss
1999, p. 1477). Invasions of nitrogenloving plants into nitrogen-limited
grasslands and shrublands appears to be
a common response to atmospheric
nitrogen deposition (Weiss and Luth
2003, p. 1), and may partly explain why
the ecosystem that existed on the San
Francisco peninsula has been so altered.
The one remaining wild
Arctostaphylos franciscana plant is
subject to multiple threats. The Presidio
Trust Act contains a sunset clause that
could result in the transfer of Presidio
holdings to the General Services
Administration (GSA) for disbursement
if the Presidio Trust operations are not
self-sufficient by 2013 (the Presidio
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Trust Act is discussed under Factor D
below). In the unlikely event that the
Presidio Trust is not self-sufficient
within that timeframe, the potential that
lands could be transferred and become
available for development presents a
threat of additional habitat loss in the
future.
Based on the best scientific and
commercial information available, we
consider the present or threatened
destruction, modification, or
curtailment of the species’ habitat or
range to be a high-magnitude and
ongoing threat to the wild population of
Arctostaphylos franciscana. The current
fragmented and degraded condition of
most remaining serpentine or
greenstone soil habitat on the San
Francisco peninsula threatens the
ability of Arctostaphylos franciscana to
expand its range. The threats of possible
development and change in
management of the habitat may further
limit the species’ propagation and
expansion, and could potentially
threaten the only remaining wild plant.
The loss of the plant’s native serpentine
chaparral habitat to development and
the curtailment of its range restrict the
species’ current and future ability to
naturally reproduce and expand its
range.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
Overutilization of Arctostaphylos
franciscana is possible due to its
popularity for landscape use, as
evidenced by the widespread use of
cultivars of this species in the
commercial nursery trade.
Arctostaphylos franciscana is
specifically recommended for use in
erosion control on steep slopes
(Theodore Payne Foundation 2009, p. 1;
Sierra Club 2011, p. 1).
The attention and media coverage
generated by the discovery of a species
thought to be extirpated from the wild
may result in efforts by the public to
visit the plant and possibly collect
cuttings or seed. Although the location
of the transplanted plant has not been
disclosed, it was planted in a heavily
used area in the Presidio, near commonuse trails with unrestricted access by the
public. The Presidio is a National Park
and is part of the GGNRA; it is open to
the public 24 hours a day, every day of
the week and receives 5 million visitors
annually. The Presidio receives heavy
use because of its proximity to the City
of San Francisco, and because the
National Park has no entrance fees and
contains restaurants, trails, and
businesses that can be accessed by car,
foot, or public transport. The Presidio
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Trust and NPS are making serious
efforts to avoid disclosing the location
of the translocated plant. The Presidio
Trust and NPS are concerned that
public knowledge of the plant’s location
would lead to authorized and
unauthorized group tours by plant
enthusiasts (T. Thomas, pers. comm.,
2011).
No damage to the plant has been
observed to date; however, trampling or
the taking of cuttings could occur if the
identification and location of the plant
becomes known. Similarly, another
extremely rare plant, Arctostaphylos
montana ssp. ravenii, is also located on
the Presidio. Although it was federally
listed in 1979, its location has not been
revealed to the public by the Presidio
Trust or NPS in order to protect the
plant from vandalism. There has been
no evidence of cuttings being taken from
A. franciscana or the similar A.
montana ssp. ravenii (Chasse 2011c, p.
3); however, the fact that the sole
remaining wild A. franciscana is located
in a heavily used public area subjects
this species to the threat of collection.
Based on the best scientific and
commercial information available, we
consider overutilization for commercial
and recreational purposes to be a threat
to the wild Arctostaphylos franciscana
plant. Although nursery-grown A.
franciscana are available to residents for
use in private gardens, collection of the
wild plant is a threat to the species, and
we expect it may be a threat in the
future, particularly if the location of the
plant becomes known to the public.
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C. Disease or Predation
Disease
Transplantation of the single wild
Arctostaphylos franciscana plant may
have caused stress to the plant, and
thereby made it more susceptible to
predation and disease. In transplanted
plants, stress and root damage may
occur from a variety of factors,
including soil compaction from foot
traffic around the plant (Hammitt and
Cole 1998, p. 52), too little or too much
water, and improper planting depth;
these stressors may result in increased
susceptibility to disease (see further
discussion in Visitor Use section
below). A fungal infection called twig
blight, usually caused by
Botryosphaeria species in
Arctostaphylos, is also a potential
concern, particularly during wet years
(Service 2003, p. 69). Twig blight was
observed in the wild plant during the
winter of 2009–2010, but it subsided
during the dry summer months (Chasse
2010, p. 2). These fungi can cause both
twig blighting and perennial branch
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cankers that can eventually kill large
branches (Swiecki 2011, p. 1). While
these pathogens would not likely pose
a serious threat to a large population,
they could threaten A. franciscana
because the wild population is limited
to a single plant, and infection by this
group of fungi is one of the major factors
leading to the decline of older
Arctostaphylos sp. plants (Swiecki
2011, p. 1). Additionally, cankers
caused by Botryosphaeria are more
severe in plants that are stressed by lack
of water. The transplanted plant may
have experienced water stress due to
loss of roots during the transplanting
process (Swiecki 2011, p. 1).
Arctostaphylos franciscana is also
threatened by various pathogens in the
genus Phytophthora. An oak tree
infected with sudden oak death disease
was discovered on the Presidio in 2010
(Fimrite 2011). Sudden oak death is
caused by Phytophthora ramorum.
Phytophthora is a fungus-like organism
most closely related to diatoms and kelp
(Kingdom Stramenopila) rather than to
the true fungi (Kingdom Fungi or
Eumycota). Phytophthora ramorum has
so far been observed to cause only a
foliar blight in species of
Arctostaphylos, rather than the lethal
bark cankers that occur on members of
the black oak group (Swiecki 2012a, p.
1). However, a related species, P.
cinnamomi has presented a serious
threat to other Arctostaphylos species
and is expected to be a serious threat to
A. franciscana. Phytophthora
cinnamomi, a soil-borne pathogen, has
long been known as a world-wide threat
to commercial and ornamental plants. It
is an introduced exotic pathogen in
North America; its native range is
unknown, but is suspected to be
southeast Asia. Human-related
activities, including the international
plant trade, have facilitated the spread
of P. cinnamomi into many habitats
worldwide (Swiecki et al. in press, p. 3).
Phytophthora cinnamomi was
introduced to California early in the
20th century, and recently has been
identified as a serious threat to the
State’s native plants and their habitats
(Swiecki et al. in press, p. 3).
Phytophthora cinnamomi has been
the cause of the decline and death of
rare Arctostaphylos species, including
the federally threatened A. pallida
(pallid manzanita) in the Oakland Hills
of the East San Francisco Bay region and
the federally threatened A. myrtifolia
(Ione manzanita) near Ione in the Sierra
Nevada foothills of Amador County. The
pathogen is also noted in the decline of
other woody native species in the San
Francisco Bay area (Swiecki et al. in
press, pp. 3–5). The organism causes
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root decay but can also kill aboveground portions of some plants (Swiecki
et al. in press, p. 3). Phytophthora
cinnamomi is persistent in soil, and
once introduced to native habitat it
cannot be eradicated (Swiecki et al. in
press, p. 3). Phytophthora cinnamomi is
transmitted by contaminated shoes,
tools, and infested soil clinging to tires,
and by contaminated nursery stock,
including native plant stock. Many areas
showing plant mortality caused by P.
cinnamomi are associated with hiking
trails, landscapes with ornamental
plants, and, in one case at the Apricum
Hill Preserve in Amador County,
California, use by visitors, including
researchers, agency personnel, students,
and the general public (Swiecki et al. in
press, p. 4).
Phytophthora cinnamomi poses a
significant current and future threat to
Arctostaphylos franciscana because of
the potential for infestation caused by
the public and staff who regularly work
with the plant. It is not possible to
predict if or when the pathogen might
infect the wild plant because the disease
is generally transmitted directly or
indirectly by humans or human activity.
The pathogen could be introduced from
soil on contaminated shoes and tools, or
from cuttings of A. franciscana plants
currently grown in a number of San
Francisco Bay area nurseries that could
become contaminated. Swiecki et al. (in
press, p. 6) tested A. menziesii plants
purchased from four nurseries and
found them to be infested with four
Phytophthora species that cause root
infections or stem cankers, including P.
cinnamomi. Crown rot, which is caused
by P. cinnamomi, is known to occur in
A. myrtifolia and A. viscida (Swiecki et
al. in press, p. 3), and is a concern when
outplanting nursery-grown plants to
wild locations (Chasse et al. 2009, p.
17). However, crown rot has not been
observed in the wild A. franciscana
plant (Chasse 2010, p. 2).
Conservation proposals include
recommendations that Arctostaphylos
franciscana cuttings be planted with the
transplanted A. franciscana to facilitate
cross-pollination of the different
genotypes. Should the wild plant
become contaminated with P.
cinnamomi, the result would be the
decline and death of the wild plant and
permanent contamination of the soil
and seedbank beneath the plant. Any
seedlings that germinate from this
seedbank would also very likely be
contaminated and not survive. Any
cuttings that become contaminated are
also expected to die of the pathogen.
The Golden Gate National Parks
Conservancy Nurseries staff in charge of
propagation and care of A. franciscana
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cuttings are aware of the threat of
contamination and rigorously follow
clean procedures to prevent infection to
the cuttings or the wild plant; however,
a risk of contamination continues to
exist because current fungicides do not
eradicate 100 percent of Phytophthora
spores (Young 2010b, p. 1). The cuttings
and layers from the single wild plant
have been dispersed to seven different
locations and growers, which, while
decreasing the risk of complete loss of
plant material, also increases the risk of
exposure to disease.
Phytophthora cinnamomi is not the
only introduced soil-borne
Phytophthora species that may threaten
Arctostaphylos franciscana. Swiecki
(2011, p. 1; 2012b, p. 1) notes that at
least five other species of Phytophthora
associated with the decline and death of
woody plants have been found in the
Crystal Springs watershed 27 to 40
kilometers (km) (17 to 25 miles (mi))
south of the Presidio. These nonnative
Phytophthora species include P.
cambivora, P. cactorum, and P.
megasperma; all are known to occur in
natural and cultivated landscapes and
are common in nursery stock (Swiecki
2011, p. 1). Phytophthora cinnamomi
and P. cambivora have been detected in
China Camp State Park, 22.4 km (14 mi)
north of the Presidio, and P. cinnamomi
has been found in the East Bay area 24
km (15 mi) east of the Presidio. Because
several of these soil-borne pathogens
have become established in the San
Francisco Bay area, the likelihood is
increased that one or more could be
introduced to the vicinity of the wild
Arctostaphylos franciscana plant
(Swiecki 2011, p. 1).
Predation
After being transplanted, the wild
plant became severely infested with the
larvae of a native leaf roller moth
(Argyrotaenia franciscana) (Estelle
2010, p. 1). Treatment for the infestation
was hand removal of the larvae and all
infected leaves, which resulted in the
removal of some of the new growth on
the plant (Estelle 2010, p. 1; Young
2010a, p. 1). A parasitic wasp emerged
from one captured leaf roller moth larva,
indicating that the moth has natural
enemies (Frey 2010, p. 2). The moth has
not been known to kill plants and does
not appear to be a serious threat at this
time; however, the moth species was
found to have five overlapping
generations in a year (Estelle 2010, p. 1).
Monthly removal of moth larvae and
pupae is conducted as needed (Estelle
2012a, p. 1). The leaf roller moth
infestation in early 2010 did not
permanently damage the plant, and new
growth was observed (Frey 2010, p. 2).
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Fewer leaf roller moth larvae were seen
on the wild plant in 2011 than in 2010
(Estelle 2012a, p. 1).
Damage to Arctostaphylos franciscana
branches by California voles has been
observed by Presidio Trust staff (Chasse
2011c, p. 2). Several voles have been
observed in and around the wild A.
franciscana plant, and some branch
dieback has been attributed to gnawing
by voles and other rodents (Chasse
2011c, p. 2).
Based on the best scientific and
commercial information available we
consider the effects from disease and
predation to be a threat to
Arctostaphylos franciscana. Infection of
the plant by Phytophthora cinnamomi
or other Phytophthora species has been
determined to be a serious threat to A.
franciscana because only one plant
occurs in the wild, the disease is easily
and quickly spread by multiple vectors,
and at least six species of Phytophthora
are known to be present in the vicinity
of the San Francisco peninsula.
Additionally, we consider predation to
be a relatively minor but ongoing threat
to the wild population of the species.
Although the leaf roller moth has not
been known to kill Arctostaphylos
species, the moth produces five
overlapping generations per year and
severely damaged the leaves in 2010.
Predation on branches by California
voles has occurred and is also relatively
minor but ongoing threat.
D. The Inadequacy of Existing
Regulatory Mechanisms
Regulatory mechanisms protecting
Arctostaphylos franciscana derive
primarily from the location of the single
known wild plant on GGNRA lands on
the Presidio, which are administered by
the Presidio Trust. The Presidio Trust
was established by the Presidio Trust
Act of 1996 to manage the leasing,
maintenance, rehabilitation, repair, and
improvement of property within the
Presidio (Presidio Trust Act, as
amended, sec. 104(a)). The Presidio
Trust is directed to preserve the natural,
scenic, cultural, and recreational
resources on the Presidio, but also is
directed to ensure that the Presidio
becomes financially self-sufficient by
2013 (Presidio Trust 2002, pp. 1, 2, 12).
The Presidio Trust Act directed that the
Presidio Trust design a management
program to reduce NPS expenditures
and increase revenues to the Federal
Government to the maximum extent
possible (Presidio Trust Act, pp. 5, 6).
The Presidio Trust Management Plan
was published in May 2002. The
Presidio Trust manages most of the
Presidio (Area B), and NPS retains
jurisdiction over Area A as defined in
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the Presidio Trust Management Plan
(Presidio Trust 2001, p. 3). The Presidio
Trust and NPS coauthored the Presidio
Vegetation Management Plan. For
special status plants, the plan provides
an objective to preserve and enhance
rare plant habitats by evaluating
species-specific habitat needs, giving
high priority to actions that preserve
and enhance those habitats (Presidio
Trust 2001, Chapter 3, unpaginated).
Federal regulations for the Presidio
Trust, which offer some protection to
Arctostaphylos franciscana, include
prohibitions on disturbing, injuring,
removing, possessing, digging, defacing,
or destroying from its natural state, any
plant or parts thereof. Unauthorized
introduction of plants and plant seeds is
also prohibited, offering limited
protection against invasive, nonnative
species. Additional regulations require
that special events be permitted by the
Presidio Trust, and provide for
restricting visitor use to address
resource conflicts (36 CFR part 1002).
The Presidio Trust is a new model for
National Park management in that the
Presidio Trust is directed to preserve the
natural, scenic, cultural, and
recreational resources on the Presidio
and at the same time ensure that the
Presidio becomes financially selfsufficient by 2013 (Presidio Trust 2002,
pp. 1, 12). This means that generation of
revenue is a consideration for the
Presidio Trust’s activities, as well as
resource protection. The cost of
operation and care are higher for this
park than for most National Parks
because of the Presidio’s large number
of structures and cultivated landscapes
(Presidio Trust 2011, unpaginated). The
mission of NPS on the Presidio, as
stated in the Golden Gate National
Recreation Area Addition Act of 1992
(16 U.S.C. 460bb), although similar to
the Presidio Trust Act regarding the
protection of natural, historic, scenic,
and recreational values, does not
include the mandate to ensure that the
Presidio becomes financially selfsufficient.
The future status of the Presidio as
National Park land is uncertain, as
explained in the Presidio Trust Act’s
section 104(o) (Reversion), which states:
‘‘If, at the expiration of 15 years, the
Trust has not accomplished the goals
and objectives of the plan required in
section 105(b) of [the Presidio Trust
Act], then all property under the
administrative jurisdiction of the Trust
pursuant to section 103(b) of [the
Presidio Trust Act] shall be transferred
to the Administrator of the General
Services Administration to be disposed
of in accordance with the procedures
outlined in the Defense Authorization
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Act of 1990 (104 Stat. 1809), and any
real property so transferred shall be
deleted from the boundary of the
Golden Gate National Recreation Area.
In the event of such transfer, the terms
and conditions of all agreements and
loans regarding such lands and facilities
entered into by the Trust shall be
binding on any successor in interest.’’
This clause indicates that lands
currently considered National Parks
lands could be disbursed to the private
sector and subject to development
within the near future. The Presidio
Trust states, however, that since 2004,
the Trust’s earned revenue has offset
operating costs and expects that the
Presidio will meet the goal of being a
self-sustaining National Park in 2012
(Middleton 2011, p. 2).
Arctostaphylos franciscana is not
listed under the California Endangered
Species Act. The conservation plan and
MOA are not regulatory in nature and
not legally enforceable by third parties
(Caltrans 2009, p. 8; Chasse et al. 2009,
p. 3), limiting their usefulness in
enforcing protections for the plant.
Although general protections are
provided for plants on National Parks,
no regulatory language in any Park
Service or Presidio Trust documents
specifically addresses protection of A.
franciscana.
Based on the best scientific and
commercial information available, we
consider the inadequacy of existing
regulatory mechanisms not to be a threat
to the species.
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E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Potential threats to Arctostaphylos
franciscana include changes in
environmental conditions resulting from
climate change, trampling or
disturbance by people visiting the
Presidio, altered fire regime, loss of
genetic diversity, loss of pollinators, and
stochastic (chance) events.
Climate Change
Our analyses under the Act include
consideration of ongoing and projected
changes in climate. The terms ‘‘climate’’
and ‘‘climate change’’ are defined by the
Intergovernmental Panel on Climate
Change (IPCC). ‘‘Climate’’ refers to the
mean and variability of different types
of weather conditions over time, with 30
years being a typical period for such
measurements, although shorter or
longer periods also may be used (IPCC
2007, p. 78). The term ‘‘climate change’’
thus refers to a change in the mean or
variability of one or more measures of
climate (e.g., temperature or
precipitation) that persists for an
extended period, typically decades or
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longer, whether the change is due to
natural variability, human activity, or
both (IPCC 2007, p. 78). Various types
of changes in climate can have direct or
indirect effects on species. These effects
may be positive, neutral, or negative and
they may change over time, depending
on the species and other relevant
considerations, such as the effects of
interactions of climate with other
variables (e.g., habitat fragmentation)
(IPCC 2007, pp. 8–14, 18–19). In our
analyses, we use our expert judgment to
weigh relevant information, including
uncertainty, in our consideration of
various aspects of climate change.
Changes in environmental conditions
resulting from climate change may
cause presently suitable habitat to
become unsuitable for endemic
California plants, due to projected
changes in temperature and rainfall
(Loarie et al. 2008, pp. 1–2). A U.S.
Geological Survey (USGS) study in
National Park lands in northern
California and Oregon is underway to
examine trends in climate, ocean
conditions, and other features (Madej et
al. 2010, p. 7). In these National Park
lands, variation in abiotic factors (for
example, precipitation, fog, and air and
ocean temperatures) regulates many
ecological processes, including the
distribution of vegetation and frequency
of disturbance from fires, floods,
landslides, and pest species. The
preliminary results of the USGS study
show an increase in average maximum
summer air temperatures at GGNRA,
near the Presidio (Madej et al. 2010, p.
24).
Summer fog and overcast along the
California coast has been identified as
ecologically important to endemic plant
species by increasing water availability
during the dry summer months,
reducing loss of water from leaves
(evapotranspiration), and decreasing the
frequency of drought stress (Fischer et
al. 2009, pp. 792–794). Fog frequency
along the Pacific coast is highest in
north and central California and
declines in Oregon and southern
California (Johnstone and Dawson 2010,
p. 4534). Climate change may be
affecting the amount and duration of fog
and cloud cover along the California
coast including within the San
Francisco Bay area. Mean fog frequency
in the California region, quantified by
cloud ceiling height measured at
airports, has decreased since 1951
(Johnstone and Dawson 2010, p. 4535).
Research by Vasey (2010, p. 1) suggests
that most coastal endemic
Arctostaphylos species are more
vulnerable to drought stress than those
found in interior California, and could
be threatened by a decrease in coastal
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summer fog. He found that obligateseeding Arctostaphylos species, such as
A. franciscana, are better hydrated in
areas that receive fog. He also found that
coastal obligate-seeding species are
more vulnerable to vascular cavitation
(blockage forming in water vessels in
the plant) when the rate of water loss
through the leaves becomes too great,
such as during drought (Vasey 2010, p.
1). This disruption of water flow can
lead to branch death and possibly death
of the entire plant (Vasey 2010, p. 1).
Reduced soil moisture from decrease
in summer fog may also result in
reduced seed germination and seedling
survival. Additionally, the ability of
Arctostaphylos franciscana to respond
to future climate changes by
establishing new plants in new habitat
may be limited because of the plant’s
association with serpentine and
greenstone bedrock outcrops (Service
2003, pp. 95, 96), and because soils
derived from serpentine and greenstone
bedrock on the peninsula are limited in
area and largely fragmented (Chasse
2010, p. 1). Natural movement of the
species by seed dispersal to reach
cooler, moister areas to the north would
be impeded by barriers such as the San
Francisco Bay.
Increased temperatures within
Arctostaphylos franciscana habitat
could also result in higher soil
temperatures that would favor
Phytophthora cinnamomi, which
reproduces best at warmer soil
temperatures. Higher temperatures
would also increase the likelihood of
water stress on A. franciscana,
increasing its susceptibility to other
Phytophthora species (Swiecki 2011, p.
1).
Alteration of the Natural Fire Regime
In addition to soil type and climate,
fire plays a critical role in the
determination of plant distribution
(Keeley 2007, p. 19). The chaparral
plant community, of which
Arctostaphylos is an important member,
is adapted to specific fire regimes that
vary in different parts of California. In
the San Francisco East Bay region, the
current fire return interval is estimated
at about 100 years (Keeley 2007, p. 20).
Factors that affect the fire frequency in
the San Francisco Bay area include a
short fire season, moist climate, the
local human population density, and
changes in human behavior. Due to
prevailing ocean winds and frequent
fogs, the average relative humidity along
the coast is moderate to high throughout
the year. The exceptions typically occur
in the fall, when changing prevailing
weather patterns allow dry northeasterly
winds from the State’s interior to reduce
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humidity in the coastal area to around
20 percent, thereby creating dry and
windy conditions that typify high fire
danger (GGNRA 2005, pp. 136, 140).
Fire frequency in the San Francisco
Bay area has varied substantially in the
last several thousand years. Not only
have the fire regimes changed with
changing climate, fire regimes have
changed as patterns of human
utilization of the landscape have
changed. Disturbances by fire occurred
at long intervals in the prehuman
period, then at shorter intervals during
the late Native American and SpanishMexican periods, and at moderate
intervals during the European
settlement period. Fire disturbance
intervals since the 1900s have generally
returned to long intervals in the modern
period due to active fire suppression
(GGNRA 2005, pp. 144–147). The
natural fire regime has been heavily
altered by the urbanization of San
Francisco and fragmentation of
remaining undeveloped lands. Nearly
all land within the City of San Francisco
has been developed, with the exception
of small, isolated parcels and
undeveloped hilltops. Lands
administered by NPS and the Presidio
Trust are surrounded by other land uses,
and are close to the wildland-urban
boundary where landscape plants and
nonnative plants contribute to
vegetative buildup (GGNRA 2005, pp.
130–131) that can increase fire danger.
Additionally, fire suppression over the
last 100 years has led to an increase in
crown and surface fuels, which
contribute to high-intensity fires
(GGNRA 2005, p. 147). In spite of the
increased fire danger on these managed
lands, they could eventually be
identified as suitable for outplanting
Arctostaphylos franciscana seedlings
due to the limited amount of remaining
habitat.
As stated above in the Species
Information section above,
Arctostaphylos franciscana is an
obligate-seeding species and reproduces
primarily from seed rather than from
burls after a fire (Vasey 2010, p. 1). Two
opposing types of changes in fire
frequency can threaten chaparral
species such as Arctostaphylos
franciscana. First, ‘‘senescence risk’’
occurs when too little fire leads to the
loss of a species dependent on fire for
regeneration. The second, ‘‘immaturity
risk,’’ is a threat primarily to obligateseeding species such as A. franciscana.
In this case, wildfires that occur too
frequently may kill plants before they
can reach reproductive maturity and
produce seed (Keeley 2007, p. 18).
Wildfire can substantially reduce the
number of live seeds in the soil (Odion
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and Tyler 2002, p. 1). Odion and Tyler
(2002 p. 1) found that a controlled burn
in a 40-year-old stand of A. morroensis
(Morro manzanita), a species also
occurring in maritime chaparral,
reduced the seedbank to 33 percent of
that which had accumulated in the soil
since the previous burn 40 years earlier.
Three years after the burn, the new
population of A. morroensis that had
germinated from the seedbank was less
than half the size of the original
population (Odion and Tyler 2002, p. 1).
Odion and Tyler (2002 p. 2) concluded
that if viable seed densities in the soil
are low because fires are too frequent to
allow seeds to accumulate in the soil,
the population may risk extinction.
The fire return interval for this
general area, and, therefore, for
Arctostaphylos franciscana, is currently
approximately 100 to 125 years (Parker
pers. comm., 2011; Vasey 2011a, p. 1).
The long fire return interval is not
thought to be a threat to the mature A.
franciscana plant at the Presidio or to
any seedlings likely to be outplanted on
the Presidio in the future. Infrequent fire
would allow the mature plant at the
Presidio to produce seed and build up
a sufficiently large seedbank to
withstand seed loss from wildfire, and
would allow the growth of outplantings
in other suitable areas. However, if fire
continues to be excluded from the
plant’s location at the Presidio and the
fire return interval greatly exceeds the
natural return interval, over time the
loss of fire may also result in the loss
of the mature plant and individual
outplanted seedlings due to competition
by other plants, including nonnative
plants, that could encroach upon the
manzanita.
Other aspects of the altered fire
regime within the remaining
undeveloped lands of San Francisco
pose greater threats to the species.
Alteration of the fire regime has led to
an increase in crown and surface fuels
in some areas, leading NPS fire planners
to conclude that it is difficult to predict
the effects of the changed fire regime,
given the trend to warmer and drier
climate conditions (Johnstone and
Dawson, 2010, p. 4535; Madej et al.
2010, p. 24) and the relationship
between climate and fire frequency
(GGNRA 2005, pp. 147, 148). In the
past, large fires have occurred within
areas that are typically subject to
maritime climatic conditions. Such fires
include the 1923 Berkeley Fire, the
October 1991 Oakland Fire (Keeley
2005, p. 286) that burned 607 ha (1,500
ac), the October 1995 fire at Point Reyes
National Seashore that burned 4,999 ha
(12,354 ac) (GGNRA 2005, p. 151), and
the 1,133-ha (2,800-ac) 2009 Lockheed
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Fire north of the City of Santa Cruz (The
Associated Press 2009). On the Presidio,
fire history data show that 17 fires
occurred between 2000 and 2009, with
no fires in some years and as many as
5 fires in other years. All fires were
contained at 0.04 ha (0.1 ac) or less (A.
Forrestel, pers. comm., 2011a, 2011b). In
the same period, approximately four
wildfires occurred in the Marin
Headlands, directly north of the
Presidio across the Golden Gate, while
recent fire history records for all areas
of the GGNRA show the potential for
larger wildfires in the maritime zone
(GGNRA 2005, pp. 150–155).
Although the Presidio is located
within a highly urbanized setting,
substantial areas of open space within
the Presidio itself and within the
adjacent GGNRA lands contain an
interspersed mixture of vegetative types,
including native vegetation, landscaped
grounds, and forest (GGNRA 2005, pp.
190–199; Presidio Trust 2011,
unpaginated). Grasslands are now
dominated by nonnative annual grasses
and forbs, which burn with greater
intensity and at a more rapid rate of
spread than grasslands dominated by
native species (GGNRA 2005, p. 192).
According to a fire model prepared by
the GGNRA, areas that they manage on
the western and southwestern borders of
Presidio Trust lands present a moderate
and moderate-high fire hazard (GGNRA
2005, p. E–7). The altered fire regime
may result in infrequent fires that burn
larger and hotter than previously, with
the potential for greater loss of the
seedbank. Alternatively, the incidence
of wildfire could increase, which would
be detrimental to Arctostaphylos
franciscana by killing mature plants,
seedlings, and seeds in the seedbank. In
obligate-seeding species, such as A.
franciscana, fire normally kills the adult
plants, which are then replaced by
plants that germinate from seed in the
soil seedbank. A wildfire that would kill
the single wild A. franciscana plant
would be an especially serious threat to
the future of the species because no A.
franciscana seedbank has been found in
soil collected from the area beneath the
wild plant (Young 2011, p. 1).
Visitor Use
Impacts due to visitor use could harm
the wild plant. The translocated wild
plant has been planted in an active
native plant management area that
receives heavy public use, although it is
protected from public access by a post
and cable fence and is monitored
(Chasse et al. 2009, pp. 20–28). The post
and cable fence is placed along an
adjacent trail so that people do not enter
the immediate area around the plant;
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however, an event in which a visitor
treads on the plant could result in
damage to the wild plant. Over time,
incremental damage could result in the
decline of the plant. The fence appears
to be effective, although its wire mesh
has been bent either by employees and
volunteers or by the general public
crossing the fence (Estelle 2012b, p. 2).
Presidio Trust staff has stated that, on a
few occasions, volunteers and members
of the general public have asked
permission to visit and photograph the
plant, and that volunteers who work
with the plant have been requested to
not disclose its location (Estelle 2012c,
p. 1). As noted under Factor B, the
Presidio Trust and NPS have made
serious efforts not to reveal the location
of Arctostaphylos franciscana because
they are concerned that public
knowledge of its location would attract
large numbers of plant enthusiasts who
may damage the A. franciscana and
compact the soil (Thomas, pers. comm.,
2011). If trampling of the A. franciscana
occurs, the Presidio Trust could take
three protective actions: a fence could
be placed around the plant, interpretive
signs could be placed near the plant,
and volunteers or interns could be made
available to talk to visitors (Thomas,
pers. comm., 2012).
The wild Arctostaphylos franciscana
plant may be susceptible to damage
from soil compaction due to foot traffic.
Roots grow into soil to maintain
stability and extract water and nutrients;
however, soil compaction increases the
resistance of the soil to root penetration
and thus diminishes the plant’s ability
to extract sufficient water and nutrients
(Hammitt and Cole 1998, p. 52). Soil
compaction also reduces water
infiltration rates and soil aeration by
collapsing the larger pores in the soil.
Reduced soil oxygen levels from loss of
soil pores also can impact root growth,
which would further reduce water and
nutrient uptake (Hammitt and Cole
1998, p. 52). Additionally, soil
compaction has been found to cause
considerable damage to mycorrhizal
fungi in seedling roots (Waltert et al.
2002, p. 1). As noted in the Historical
Distribution and Habitat section, most
Arctostaphylos species form strong
symbiotic associations with soil
mycorrhizal fungi, which develop an
external sheath surrounding the plant’s
roots. All water and nutrients pass
through this sheath to the plant’s roots
rather than directly from the soil to the
plant’s roots (Chasse 2009, p. 12).
Damage from soil compaction would not
only impact the wild plant by reducing
its ability to take up water and
nutrients, but could also reduce the
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survival of seedlings near the wild
plant.
Soil compaction also favors the
growth of Phytophthora. Poor drainage
resulting from compaction facilitates the
dispersal of swimming zoospores that
infect the host plant (Swiecki 2011, p.
2). Additionally, anaerobic (lack of
oxygen) stress associated with saturated
soil conditions increases the
susceptibility of roots to Phytophthora
infections (Swiecki 2011, p. 2).
Vandalism
The location of the Arctostaphylos
franciscana plant within the Presidio is
near common-use trails and an area
available for private and public events.
Threats to A. franciscana include
damage from vandalism. Vandalism to
trees was reported in the Presidio in the
early 2000s (Thomas pers. comm. 2011).
Severe vandalism was observed in
Golden Gate Park, located
approximately 1.5 mi (2.4 km) south of
the Presidio, in summer 2010, when
more than 40 trees and 30 rose bushes
were destroyed by unknown persons for
unknown reasons (Gordon 2010,
unpaginated; King 2010, unpaginated).
The post and cable fence that protects
the wild A. franciscana plant is
approximately 30 ft (9.1 m) from the
plant and is not constructed to
completely exclude visitors. In the
unlikely event that vandalism occurs,
the results could be serious because
there is only one wild plant.
Stochastic Events and Small Population
Size
Chance events constitute a serious
threat to Arctostaphylos franciscana.
Because the known population of A.
franciscana in the wild is currently
limited to a single plant, the species is
extremely vulnerable to stochastic
events—normal but damaging
environmental perturbations and
catastrophes such as droughts, storm
damage, disease outbreaks, and fires,
from which large, wide-ranging
populations can generally recover, but
which may lead to extirpation of small,
isolated populations (Gilpin and Soule
1986, pp. 25–31). The majority of the
remaining habitat associated with A.
franciscana occurs within rock outcrops
on hilltops or slopes surrounded by
development or along coastal cliffs.
These areas, because of their limited
size and proximity to developed areas,
are more likely to experience
inadvertent fire or environmental
degradation (altered hydrologic regime;
increased introduction of nonnative,
invasive plants; and increased spread of
disease). The nature of the habitat
associated with A. franciscana (rock
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outcrops, thin soils, sloped or hilltop
terrain) may also increase the effects of
drought. By nature these habitats
generally do not have the water-holding
capacity of deeper soiled, level habitats.
Because some of the remaining habitat
associated with the species is along
coastal bluffs or on hillsides, these areas
may also be more susceptible to
landslides or erosion during excessively
wet precipitation events. As a result, we
consider stochastic events to be of
significant threat for this species.
Any new population that starts from
the single wild plant is likely to have
reduced genetic variation compared to
historical populations. Even if the
number of plants increases, it may not
reverse the previous genetic loss, known
as the bottleneck effect (Allendorf and
Luikart 2007, p. 158). Bottlenecks
generally have a greater and more
lasting effect on the loss of genetic
variation in species with slow growth
rates (long-lived species with few
offspring) (Allendorf and Luikart 2007,
p. 133). The age of the single wild
Arctostaphylos franciscana plant is
estimated at 60 years, and no other A.
franciscana plants or seedlings were
found associated with the wild plant.
Reduced genetic variation may result in
the inability of future generations of the
plant to adapt to changes in habitat,
such as decrease in fog and increase in
temperature (see Climate Change
discussion above) or loss of pollinators
(see discussion below). While
Arctostaphylos franciscana may be
capable of self-pollination, in general,
self-pollination results in decreased
genetic variation in the offspring of a
plant (Allendorf and Luikart 2007, p.
123). Therefore, loss of genetic variation
is expected if A. franciscana is
dependent on self-pollination to
produce seed. Based on the above
discussion, we have determined that the
loss of genetic variation is a significant
threat for this species.
The wild plant is also threatened by
the Allee effect, a decline in population
growth rate due to declining plant
density (Akcakaya et al. 1999, p. 86).
¸
For the wild Arctostaphylos franciscana
plant, the Allee effect may result from
a lack of other available A. franciscana
plants with which to cross-pollinate and
produce viable seed. The wild plant, the
single remaining individual of its
species in the wild, is currently
dependent on its ability to selfpollinate, which may be limited, and
the efforts of researchers and Presidio
staff to provide additional plants of
different genotypes (if they are proven
to be A. franciscana) from botanical
garden specimens to cross-pollinate
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with the wild plant to produce new
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Loss of Pollinators
Suitable pollinators may be critical for
seed production for this obligateseeding species. If pollinators are
absent, or present in insufficient
numbers, there may be a lack of viable
seeds to develop and maintain the
seedbank. In a study of the effects of
habitat fragmentation on a non-selfpollinating plant (Lennartsson 2002, pp.
3065, 3066, 3068), the author found that
fragmented populations exhibited
dramatically reduced seed set and
population viability, both of which were
caused by a reduction in the number of
pollinators.
Pollinators have been observed on the
wild A. franciscana plant; however, no
surveys have been completed to identify
the most important pollinators. The
most frequent pollinators seen have
been bees and bumblebees.
Hummingbirds and butterflies have also
been observed visiting the flowers,
likely because few other plants are
blooming during the winter months
when A. franciscana blooms (Vasey,
pers. comm. 2010). Although the loss of
seed produced in a single year would
not likely lead to the extirpation of the
species, the continued reduction of the
seed crop or dependence on selfpollination would reduce the seedbank,
genetic variation, and the potential for
population expansion.
Hybridization
Cultivars of Arctostaphylos
franciscana are used in the commercial
nursery trade. The cultivars (varieties of
a plant produced and maintained by
cultivation) are likely descended from
some of the last wild A. franciscana
plants known to exist in the 1940s, and
are located in at least four botanical
gardens (Chasse et al. 2009, pp. 7, 8).
Because hybridization between diploid
species of Arctostaphylos is well
recognized (Chasse et al. 2009, p. 5),
there is a good chance that many of
these commercially available specimens
have resulted from hybrid seed. Because
of the threat of cross-pollination from
hybrids or other species (Allendorf et al.
2001, pp. 613, 618–621), any
propagation or reintroduction programs
for A. franciscana must account for
subsequent contamination of the A.
franciscana gene pool. The conservation
plan takes this into account by
recommending that future outplantings
of nursery-raised cuttings or seedlings of
the recently discovered A. franciscana
plant avoid areas that could facilitate
cross-pollination (Chasse et al. 2009, p.
31). Appropriate outplanting areas will
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be determined by A. franciscana
experts, in cooperation with NPS, the
Presidio Trust, and the Golden Gate
National Parks Conservancy (Chasse et
al. 2009, p. 31). Although crosspollination of the wild plant with
hybrids and the production of hybrid
seed is possible, we do not know if this
is a substantial threat to the species.
Based on the best scientific and
commercial information available, we
consider that Arctostaphylos
franciscana is negatively impacted by
other natural or manmade factors
affecting its continued existence which
include changes in environmental
conditions resulting from climate
change, altered fire regime, soil
compaction from visitor use, vandalism,
loss of genetic diversity, loss of
pollinators, stochastic events, effects of
small population size, and
hybridization. Cumulatively, we
consider these threats to be significant
and ongoing.
Cumulative Impacts
Some of the threats discussed in this
finding could work with one another to
cumulatively create situations that
potentially impact Arctostaphylos
franciscana beyond the scope of the
individual threats we have already
analyzed. In particular, climate change
may exacerbate many of the threats
discussed in this final rule. For
example, warmer, drier conditions in
the range of the species could result in
not only less summer fog and increased
water stress leading to plant death, but
could also create more suitable
conditions for infection by
Phytophthora species and result in more
fires. The loss of native habitat due to
urban development within the range of
A. franciscana has likely reduced
pollinator nesting areas and numbers of
native plants that provide nectar and
pollen. Climate change could increase
the loss of pollinators if the abundance
of flowers preferred by pollinators
decreases and the synchrony of bloom
periods and pollinator emergence is
disrupted. Although there currently are
no data available regarding changes in
plant bloom periods or emergence dates
of pollinators in the Presidio in
response to climate change, Forister and
Shapiro (2003, p. 1130) found that over
a period of 31 years warmer and drier
winter conditions were associated with
earlier butterfly appearance in the
Central Valley of California. The ability
of A. franciscana to self-pollinate may
be limited (Parker 2011, p. 1); therefore,
we expect that bumblebees, bees, and
other insects are likely needed for A.
franciscana to produce seed. Nitrogen
enrichment of the soil from atmospheric
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deposition may encourage the growth of
nonnative, invasive grasses in the
vicinity of the wild plant. The grasses
could, in turn, provide additional
habitat for rodents such as California
voles that feed on the wild plant.
Determination
We have carefully assessed the best
scientific and commercial information
available regarding past, present, and
future threats to Arctostaphylos
franciscana. The primary threat to A.
franciscana is from the present or
threatened destruction, modification, or
curtailment of the species’ habitat or
range (Factor A). All original occupied
habitat of the species has been lost, and
its current range has been reduced to a
single location that supports a single A.
franciscana plant. The last wild plant
was moved from its native habitat,
which was subsequently destroyed
during a highway construction project,
and transplanted to natural habitat on
the Presidio in San Francisco. Limited
remaining suitable habitat is available to
support a viable population of the
species. Although greenstone and
serpentine soils remain on the
peninsula, the majority of this land has
been fragmented and may be subject to
edge effects and nitrogen deposition.
Additionally, the possible transfer of
Presidio lands to the GSA and the
private sector may result in potential
future loss of the plant or modification
of its habitat.
Overutilization (Factor B) is a threat
because the current known wild
population consists of one individual
plant, and Arctostaphylos plants are
popular for landscaping and other
horticultural purposes. Arctostaphylos
franciscana is thus vulnerable to
overcollection or damage if visitors
harvest cuttings or seeds.
Disease and predation (Factor C).is
also a threat to Arctostaphylos
franciscana. Stress from transplanting
the wild plant may have weakened the
plant and made it more susceptible to
disease and predation. The plant was
heavily infested with a native leaf roller
moth after being transplanted; however,
the caterpillars and damaged foliage
were removed and the plant has
produced new foliage and flowers.
Minor damage to Arctostaphylos
franciscana branches from gnawing by
California voles and other rodents has
also been observed. Twig blight, a
fungal infection, was observed on the
plant during the winter of 2009–2010,
but the infection subsided during the
dry season. Infection by Phytophthora
species, especially Phytophthora
cinnamomi, is a serious and lethal
problem among Arctostaphylos species
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in the wild and in the native plant
nursery trade. Phytophthora cinnamomi
cannot be controlled once introduced to
a plant or habitat, and results in plant
death. Many A. franciscana cuttings are
being grown in commercial or
university nurseries for outplanting
with the wild plant. Although the use of
clean propagation techniques has been
requested by the staff in charge of the
project, the risk of infection of the
cuttings and wild plant by P.
cinnamomi is still a threat. At least six
other species of Phytophthora are also
found south of the San Francisco
peninsula and could be introduced into
the vicinity of the wild plant. In
addition, the pathogen that causes
sudden oak death has been discovered
in the Presidio; however, the threat of
this disease to A. franciscana is likely
not severe.
Existing regulatory mechanisms
(Factor D) afford certain protections for
Arctostaphylos franciscana because the
plant is located on lands administered
by NPS, GGNRA, and the Presidio Trust.
However, as mentioned above, these
protections are not specific to A.
franciscana. Because no existing
regulatory mechanisms exist specific to
A. franciscana, we do not consider the
existing regulatory mechanisms to be
inadequate to protect the species.
Other natural or manmade factors
affecting Arctostaphylos franciscana’s
continued existence (Factor E) include
environmental effects resulting from
climate change, alteration of the natural
fire regime, soil compaction from visitor
use, vandalism, loss of genetic diversity,
stochastic events, small population size,
loss of pollinators, and hybridization are
also threats to this species. Changes in
the climate are expected to include
increased air temperature and reduced
summer fog, both resulting in warmer
and drier conditions to which the plant
may be less well-adapted. Additionally,
climate change may result in divergence
between the timing of flowering of A.
franciscana and the availability of
suitable pollinators, negatively affecting
the plant’s ability to set seed. Climate
change may also reduce pollinator
species and numbers. Warming and
drying of the plant’s habitat would
likely also increase the frequency of
wildfire, which could result in death of
the wild plant and its future seedlings
if fire occurred before the plants were
able to produce viable seeds. Loss of
mature Arctostaphylos plants to fire is a
natural phenomenon; however, this
species is currently represented by a
single mature plant. Therefore, to our
knowledge, the loss of the plant would
result in extinction of the species in the
wild. Loss of genetic diversity has likely
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already occurred due to the reduction of
the species to a single wild plant and is
expected to continue because this
generally outcrossing species will be
limited to self-pollination. Reduced
genetic diversity may also limit the
species’ ability to adapt to changes in
habitat, such as those resulting from
climate change or loss of pollinators.
The species is extremely vulnerable to
stochastic events such as droughts,
storm damage, and fires, from which
large wide-ranging populations can
generally recover, but which would
likely drive a species consisting of a
single plant to extinction.
Based on our evaluation of the best
available scientific and commercial
information regarding the past, present,
and future threats faced by
Arctostaphylos franciscana, we have
determined that the continued existence
of A. franciscana is threatened by
overutilization for commercial and
recreational purposes, disease, and
predation, climate change, alteration of
the natural fire regime, soil compaction
from visitor use, vandalism, loss of
genetic diversity, stochastic events,
small population size, loss of
pollinators, and hybridization. Because
the species faces these threats
throughout its extremely limited range,
we find that A. franciscana is in danger
of extinction throughout its entire range
and, therefore, it is unnecessary to
analyze its status in any significant
portion of its range.
The Act defines an endangered
species as one that is in danger of
extinction throughout all or a significant
portion of its range. A threatened
species is one that is likely to become
an endangered species in the foreseeable
future throughout all or a significant
portion of its range. The species in the
wild currently exists as a single plant on
the San Francisco Presidio. Because the
range of the species is restricted to a
single plant, the risks presented by the
threats discussed herein are more
intensified than they would be were the
species more widespread or numerous.
Based on our evaluation of the best
available scientific and commercial
information, and given the current
population size (one wild plant) and
severely limited distribution throughout
its historical range, we have determined
the species is currently on the brink of
extinction in the wild and therefore is
in danger of extinction throughout all of
its range. As a result, this species meets
the definition of an endangered species
under the Act. Because the species is in
danger of extinction now due to its
limited population size and the severity
of existing threats, as opposed to in the
foreseeable future, A. franciscana meets
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54449
the definition of an endangered species
rather than a threatened species. On the
basis of our careful evaluation of the
best available scientific and commercial
information regarding the past, present,
and future threats to the species as
discussed above relative to the listing
factors, we are listing Arctostaphylos
franciscana as an endangered species
throughout its range.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain practices.
Recognition through listing results in
public awareness and conservation by
Federal, State, and local agencies;
private organizations; and individuals.
The Act encourages cooperation with
the States and requires that recovery
actions be carried out for all listed
species. The protection measures
required of Federal agencies and the
prohibitions against certain activities
are discussed, in part, below.
Section 7(a) of the Act requires
Federal agencies to evaluate their
actions with respect to any species that
is proposed or listed as endangered or
threatened and with respect to its
critical habitat, if any is designated.
Regulations implementing this
interagency cooperation provision of the
Act are codified at 50 CFR part 402.
Section 7(a)(4) of the Act requires
Federal agencies to confer with the
Service on any action that is likely to
jeopardize the continued existence of a
species proposed for listing or result in
destruction or adverse modification of
proposed critical habitat. If a species is
listed subsequently, section 7(a)(2) of
the Act requires Federal agencies to
ensure that activities they authorize,
fund, or carry out are not likely to
jeopardize the continued existence of
the species or destroy or adversely
modify its critical habitat. If a Federal
action may affect a listed species or its
critical habitat, the responsible Federal
agency must enter into formal
consultation with the Service.
Federal agency actions within the
species’ habitat that may require
conference or consultation or both, as
described in the preceding paragraph,
include land management, road
construction, and any other landscape
altering activities, such as invasive tree
and plant removal, within the known
range of the species or within any
designated critical habitat.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
E:\FR\FM\05SER1.SGM
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Federal Register / Vol. 77, No. 172 / Wednesday, September 5, 2012 / Rules and Regulations
to endangered plants. All prohibitions
of section 9(a)(2) of the Act,
implemented by 50 CFR 17.61, apply.
When this final rule becomes effective
(see DATES section above),
Arctostaphylos franciscana, the last
wild specimen (including any plants
propagated from the wild plant) and the
botanical garden specimens (those
plants previously collected from the
wild and subsequently propagated), will
be protected by all prohibitions of
section 9(a)(2) of the Act, which protects
listed plants in areas of Federal
jurisdiction such as the Presidio. Plants
that have been or are being sold in the
nursery trade or have been transplanted
into home gardens will not be
considered part of the listed entity.
These prohibitions, in part, make it
illegal for any person subject to the
jurisdiction of the United States to
import or export, transport in interstate
or foreign commerce in the course of a
commercial activity, sell or offer for sale
in interstate or foreign commerce, or
remove and reduce the species to
possession from areas under Federal
jurisdiction. In addition, for plants
listed as endangered, the Act prohibits
the malicious damage or destruction on
areas under Federal jurisdiction and the
removal, cutting, digging up, or
damaging or destroying of such plants
in knowing violation of any State law or
regulation, including State criminal
trespass law. Certain exceptions to the
prohibitions apply to agents of the
Service and State conservation agencies.
Arctostaphylos franciscana has not
been listed by the State of California.
Listing also requires Federal agencies to
avoid actions that might jeopardize the
species (16 U.S.C. 1536(a)(2)), and
provides opportunities for funding of
conservation measures and land
our reasons for this determination in the
Federal Register on October 25, 1983
(48 FR 49244).
acquisition that would not otherwise be
available to them (16 U.S.C. 1534,
1535(d)).
We may issue permits to carry out
otherwise prohibited activities
involving endangered and threatened
wildlife species under certain
circumstances. Regulations governing
permits are codified at 50 CFR 17.62 for
endangered plants, and at 17.72 for
threatened plants. With regard to
endangered plants, a permit must be
issued for the following purposes: for
scientific purposes or for enhancing the
propagation or survival of the species,
and for take to to prevent undue
economic hardship (see 50 CFR 17.63).
The primary authors of this document
are the staff members of the Sacramento
Fish and Wildlife Office (see
ADDRESSES).
Required Determinations
List of Subjects in 50 CFR Part 17
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.)
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
This rule does not contain any new
collections of information that require
approval by Office of Management and
Budget (OMB) under the Paperwork
Reduction Act. This rule will not
impose recordkeeping or reporting
requirements on State or local
governments, individuals, businesses, or
organizations. An agency may not
conduct or sponsor, and a person is not
required to respond to, a collection of
information unless it displays a
currently valid OMB control number.
National Environmental Policy Act
References Cited
A complete list of all references cited
in this rule is available on the Internet
at https://www.regulations.gov or upon
request from the Field Supervisor,
Sacramento Fish and Wildlife Office
(see ADDRESSES).
Authors
Regulation Promulgation
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as follows:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Pub. L. 99–
625, 100 Stat. 3500; unless otherwise noted.
2. Amend § 17.12(h) by adding an
entry for ‘‘Arctostaphylos franciscana’’
(Franciscan manzanita) to the List of
Endangered and Threatened Plants in
alphabetical order under FLOWERING
PLANTS, to read as follows:
■
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act of
1969 (42 U.S.C. 4321 et seq.), need not
be prepared in connection with
regulations pursuant to section 4(a) of
the Act. We published a notice outlining
§ 17.12
*
Endangered and threatened plants.
*
*
(h) * * *
Species
Historic range
Scientific name
Family
Status
*
*
U.S.A., (CA) ...............
*
Ericaceae ...................
Common name
*
When
listed
*
Critical
habitat
Special
rules
FLOWERING PLANTS
*
Arctostaphylos
franciscana.
*
Franciscan manzanita
*
E
*
809
NA
NA
*
*
*
*
*
*
*
mstockstill on DSK4VPTVN1PROD with RULES
*
*
*
*
*
*
*
Dated: August 24, 2012.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. 2012–21742 Filed 9–4–12; 8:45 am]
BILLING CODE 4310–55–P
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Agencies
[Federal Register Volume 77, Number 172 (Wednesday, September 5, 2012)]
[Rules and Regulations]
[Pages 54434-54450]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-21742]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R8-ES-2010-0049; 4500030113]
RIN 1018-AX89
Endangered and Threatened Wildlife and Plants; Determination of
Endangered Status for Arctostaphylos franciscana (Franciscan manzanita)
Throughout Its Range
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), determine
that Arctostaphylos franciscana (Franciscan manzanita) meets the
definition of an endangered species under the Endangered Species Act of
1973, as amended (Act). This final rule implements the Federal
protections provided by the Act for this species. We are simultaneously
publishing a proposed rule to designate critical habitat for
Arctostaphylos franciscana in a separate Federal Register notice.
DATES: This rule becomes effective October 5, 2012.
ADDRESSES: This final rule is available on the Internet at https://www.regulations.gov and at the Sacramento Fish and Wildlife Office.
Comments and materials received, as well as supporting documentation
used in the preparation of this rule, will be available for public
inspection, by appointment, during normal business hours at: U.S. Fish
and Wildlife Service, Sacramento Fish and Wildlife Office, 2800
Cottage, Room W-2605, Sacramento, CA 95825; 916-414-6600 (telephone);
916-414-6712 (facsimile).
FOR FURTHER INFORMATION CONTACT: Susan Moore, Field Supervisor,
Sacramento Fish and Wildlife Office (see ADDRESSES section). If you use
a telecommunications device for the deaf (TDD), call the Federal
Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Executive Summary
Why we need to publish a rule. This is a final rule to list
Arctostaphylos franciscana as an endangered species under the
Endangered Species Act. Under the Act, if a species is determined to be
an endangered or threatened species we are required to promptly publish
in the Federal Register and make a determination on our proposal within
one year. We were petitioned in 2010 to list A. franciscana as an
endangered or threatened species. We determined in our 12-month finding
that listing was warranted, and we proposed to list the species as an
endangered species in September 2001. This final rule constitutes our
final determination for this species as required by the Act.
The basis for our action. Under the Endangered Species Act, we are
required to determine whether a species is endangered or threatened
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. We reviewed all available scientific
and commercial information pertaining to these factors in our status
review of the species and determined that the species was limited to
one plant remaining in the wild. We proposed that the species was
endangered due to threats in the five factors, as follows. The primary
threat to Arctostaphylos franciscana is from the present or threatened
destruction, modification, or curtailment of the species' habitat or
range. All original occupied habitat of the species has been lost, and
its current range has been reduced to a single location that supports a
single A. franciscana plant. Furthermore, limited suitable habitat
remains available to support a viable population of the species. The
remaining plant is vulnerable to overcollection or damage if visitors
harvest cuttings or seeds. Sudden oak death, which is caused by the
pathogen Phytophthora cinnamomi, and infections caused by other
Phytophthora species are serious threats to Arctostaphylos franciscana
because only one plant occurs in the wild and the diseases are easily
spread. Predation is an ongoing but lesser threat. Additional threats
include climate change, altered fire regime, soil compaction from
visitor use, vandalism, loss of genetic diversity, loss of pollinators,
stochastic events, effects of small population size, and hybridization.
In the proposed rule, we considered these threats to be significant and
ongoing, but we did not find that we had sufficient information
[[Page 54435]]
to determine critical habitat at the time. In this final rule, we
utilize public comments and peer review to inform our final
determination, as required under the Act.
Peer review and public comments. In this final rule, we present and
respond to peer reviewer and public comments. We obtained peer reviews
from knowledgeable individuals with the scientific expertise to review
our technical assumptions, analysis, adherence to regulations, and
whether or not we had used the best available information. These peer
reviewers generally concurred with our methods and conclusions, and
they provided additional information, clarifications, and suggestions
to improve this final rule. In particular, peer reviewers provided
information on the physical and biological features required by the
species, and on locations of remnant natural habitat that retained
these features, suggesting that proposal of critical habitat would be
determinable and prudent. Accordingly, a proposed rule to designate
critical habitat is being published concurrently with this final rule
to list the species as endangered.
Background
It is our intent to discuss only those topics directly relevant to
the listing of Arctostaphylos franciscana under the Act (16 U.S.C. 1531
et seq.) in this final rule. For further information on the species'
biology and habitat, population abundance and trend, distribution,
demographic features, habitat use and conditions, threats, and
conservation measures, please see the September 8, 2011, proposed
listing for the species (76 FR 55623) published in the Federal
Register, or the Recovery Plan for Coastal Plants of the Northern San
Francisco Peninsula (Service 2003). These documents are available from
the Environmental Conservation Online System (ECOS) (https://ecos.fws.gov/ecos), the Sacramento Fish and Wildlife Office Web site
(https://www.fws.gov/sacramento/), or from the Federal eRulemaking
Portal (https://www.regulations.gov).
Prudency Determination
In our proposed listing rule for Arctostaphylos franciscana (76 FR
55623; September 8, 2011), we stated that we believed that critical
habitat was not determinable at the time of the proposal due to a lack
of knowledge of what physical or biological features were essential to
the conservation of the species, or what other areas outside the site
that is currently occupied may be essential for the conservation of the
species. Subsequently, we requested information from the public during
the public comment period and solicited information from peer reviewers
on whether the determination of critical habitat was prudent and
determinable. We also asked for information about the physical or
biological features that are essential to the conservation of the
species and what areas contained those features or were otherwise
essential for the conservation of the species. Based on the information
we received on the physical or biological features for A. franciscana,
and information on areas otherwise essential for the species, we have
determined that the designation of critical habitat is prudent and
determinable. We are therefore proposing critical habitat elsewhere in
today's Federal Register. For more information regarding our
determination to designate critical habitat please see our response to
comments below and the proposed rule to designate critical habitat for
A. franciscana published in the Proposed Rules section of today's
Federal Register.
Species Information
Arctostaphylos franciscana is a low, spreading-to-ascending,
evergreen shrub in the heath family (Ericaceae) that may reach 0.6 to
0.9 meters (m) (2 to 3 feet (ft)) in height when mature (Chasse et al.
2009, p. 5). Its leaves are about 1.5 to 2 centimeters (cm) (0.6 to 0.8
inches (in)) long, are isofacial (have the same type of surface on both
sides), and are oblanceolate (longer than they are wide and wider
towards the tip) (Eastwood 1905, p. 201; Chasse et al. 2009, p. 39).
Its mahogany brown fruits are about 6 to 8 millimeters (mm) (0.24 to
0.32 in) wide, while its urn-shaped flowers measure about 5 to 7 mm
(0.2 to 0.28 in) long (Wallace 1993, p. 552; Service 2003, p. 57).
A closely related species, Arctostaphylos hookeri ssp. ravenii
(Presidio or Raven's manzanita), which was federally listed as
endangered on October 26, 1979 (44 FR 61909), looks similar but has a
growth habit that is more prostrate, leaves that are more rounded,
fruits that are smaller and less red in color, and flowers that are
smaller and more spherical (Service 2003, pp. 55, 57). Arctostaphylos
hookeri ssp. ravenii has recently undergone a taxonomic revision to A.
montana ssp. ravenii, and we will be referring to the listed species by
this name throughout this rule (see Genetics and Taxonomy section
below). Another somewhat similar appearing species, though not as
closely related, is A. uva-ursi (bearberry), which can be distinguished
by its lack of isofacial leaves (Chasse et al. 2009, p. 39).
In the wild, Arctostaphylos franciscana is an obligate-seeding
species (it reproduces primarily from seed rather than from burls)
(Vasey 2010, p. 1). Arctostaphylos (manzanita) species are members of
the chaparral plant community, which have a variety of triggers for
seed germination including heat, smoke, and light (Keeley 1987, p.
434). Arctostaphylos species have germinated after being exposed to
charate (ground charred wood) (Keeley 1987, pp. 435, 440), which
suggests that fire or conditions that simulate fire stimulate
germination of the seeds.
Based on work with other species of Arctostaphylos, the
establishment of successful populations of A. franciscana may require
the presence of a pollinator community (primarily bumblebees (Bombus
spp.) but also other insects), a fruit dispersal community (primarily
rodents), and a mutually beneficial soil mycorrhizal fungi community
(see Historical Distribution and Habitat below) (Parker 2011, p. 1).
The seeds of Arctostaphylos are dispersed primarily by rodents that
consume the fruits, but also by other mammals, including coyotes (Canis
latrans) and foxes (T. Parker 2011, pers. comm.; Vasey 2011a, p. 1).
Seed-eating animals such as coyotes, gray foxes (Urocyon
cinereoargenteus), red foxes (Vulpes vulpes), raccoons (Procyon lotor),
California quail (Callipepla californica), and rodents such as the
California vole (Microtus californicus) are known to occur on the
Presidio of San Francisco (Presidio), a unit of the National Park
System, on the San Francisco peninsula where A. franciscana is found
(National Park Service (NPS) 2012). Animals such as coyotes and foxes
eat the Arctostaphylos fruit and may travel long distances before
depositing their scat. Any undigested fruit left in the scat can then
be harvested by rodents and either eaten or buried. Parker (2010b, p.
1) found that 70 percent of the fruits buried by rodents were located
deeper than 2 cm (0.78 in), which is the maximum soil depth at which
seeds are typically killed by wildfire. Seed has been removed from the
wild plant, and, although it has not been directly observed, California
voles have been trapped near the wild plant and are likely responsible
for the seed harvesting (Carlen 2012, p. 1; Estelle 2012d, p. 1).
Listed Entity Analysis
The Arctostaphylos franciscana plants that exist in cultivation
fall into three categories: (1) Cuttings and rooted specimens collected
from the Laurel Hill Cemetery and transplanted to various managed
botanical gardens in
[[Page 54436]]
San Francisco, Berkeley, and Claremont prior to 1947; (2) specimens
currently propagated in greenhouses from cuttings and layers taken from
the wild plant in 2010; and (3) specimens, some of which may be of
unknown origin, sold in the nursery trade or transplanted into home
gardens. We consider the single wild plant and plants identified in (1)
and (2) above to be the listed entity under the Act. Our rationale for
not including plants identified in item (3) above is outlined below.
The Arctostaphylos franciscana plants found in botanical gardens
may represent from one to six genetically distinct plants other than
the single wild plant (Chasse et al. 2009, p. 7; Chasse 2011a, p. 1;
Chasse 2011b, p. 1; Vasey 2011b, pp. 2, 3), and cuttings from those
plants may contribute genetic material to efforts to expand the number
of wild plants. The botanical garden plants are not considered part of
the wild population and, therefore, are not considered in the
assessment of species status, although they will be considered to be
listed when this final rule becomes effective (see the DATES section
above). The cuttings and layers collected from the wild plant currently
propagated in greenhouses are being considered in the assessment of the
species' status. These cuttings from the wild plant will be planted
with A. franciscana specimens propagated in botanical gardens to
establish additional populations of the species. We have concluded that
the third category of plants, those cultivated for private or
commercial uses, will not aid in the conservation or recovery of the
species in the wild because some cultivated plants may be hybrids and
bred for landscape use and thus offer minimal contribution to
conservation.
Current Distribution
In October 2009, an ecologist identified a plant growing in a
concrete-bound median strip along Doyle Drive in the Presidio as
Arctostaphylos franciscana (Chasse et al. 2009, pp. 3, 4; Gluesenkamp
2010, p. 7). The plant's location was directly in the footprint of a
roadway improvement project designed to upgrade the seismic and
structural integrity of the south access to the Golden Gate Bridge
(California Department of Transportation (Caltrans) et al. 2009, p. 1;
Chasse et al. 2009, p. 10).
Several agencies, including the Service, established a Memorandum
of Agreement (MOA) and conservation plan for the species (see Previous
Federal Actions section below) (Caltrans et al. 2009). The conservation
partners concluded that leaving the plant undisturbed at its original
site would compromise public safety and cultural resources by the
potential curtailment or redesign of the roadway improvement project
(Chasse et al. 2009, pp. 9, 10).
The conservation plan evaluated potential translocation sites,
established procedures for preparation of the new site and for the
translocation itself, and called for management and monitoring (both
short- and long-term) of the translocated plant, with the goal of
eventually establishing self-sustaining populations of the species in
the wild (Chasse et al. 2009, pp. 23-27, 29-30). Following
recommendations in the conservation plan, the Arctostaphylos
franciscana plant was moved successfully to a new site within the
Presidio in January 2010. The Presidio site was chosen after careful
consideration of its appropriate soil type and the management and
monitoring capabilities of the NPS and the Presidio Trust. Subsequent
monitoring reports indicate the translocated plant continues to do well
at its new location (Yam 2010, pp. 1, 3-14; Young 2010a, p. 1; Young
2012, p. 1).
Historical Distribution and Habitat
Known historical occurrences and collections of Arctostaphylos
franciscana are from serpentine maritime chaparral, a plant community
dominated by Arctostaphylos and Ceanothus (California lilac) species,
on the San Francisco peninsula. This area is part of a region that
Willis Linn Jepson named the Franciscan Area, one of 10 areas he
considered to have the highest concentration of endemic plant species
in California (Jepson 1925, pp. 11-14). An endemic species is one that
is native to, and restricted to, a particular geographical area. Native
habitats on the San Francisco peninsula have been largely converted to
urban areas of the City of San Francisco, and habitat that might have
supported A. franciscana is now mostly lost to development or habitat
conversion from the introduction of nonnative plant species (Chasse
2010, p. 2; Gluesenkamp 2010, p. 7; Chasse 2011c, p. 1).
Chasse (2009, pp. 6, 7) has noted that information on the plant
community that historically included Arctostaphylos franciscana is
largely missing from the literature. Early records describe the species
as growing ``on rocky ground'' (Eastwood 1905, p. 202), on ``bare,
stony bluff on Laurel Hill Cemetary [sic]'' (Brandegee 1908), and with
coast live oak (Quercus agrifolia), coast blue blossom (Ceanothus
thyrsiflorus), and coyote brush (Baccharis pilularis) (Wieslander
1938). Arctostaphylos franciscana was also observed ``forming flat
masses over serpentine outcroppings and humus-filled gravel and
flopping down over the sides of gray and chrome rocks. Ericameria,
Baccharis, Ferns, Buckwheats, and Golden Yarrow grow among it; and over
it stand Toyons and Live Oaks.'' Additionally, A. montana ssp. ravenii
was found at nearly all A. franciscana locations. These observations,
along with the geology and climate of historical sites, indicate that
the species' historical community likely consisted of a mosaic of
coastal scrub, barren serpentine maritime chaparral, perennial
grassland, and occasional woodlands of coast live oak and toyon shrubs
and small trees (Chasse 2009, pp. 6, 7).
Arctostaphylos franciscana is considered to be endemic to the San
Francisco peninsula, and historically occurred in areas with serpentine
soils, bedrock outcrops, greenstone, and mixed Franciscan rock,
typically growing in mixed populations with A. montana ssp. ravenii
(Service 2003, pp. 95, 96; Chasse et al. 2009, p. 6). The Doyle Drive
A. franciscana site was comprised of disturbed soil over serpentinite
(Chasse et al. 2009, p. 3). Serpentine soil restricts the growth of
many plants due to its high nickel and magnesium concentrations, and
thus tends to support unique plant communities (Brooks 1987, pp. 19,
53; Service 2003, p. 16) because relatively few plant species can
tolerate such soil conditions. These conditions generally result in
semibarren soil and a lack of competing plants, which benefits
serpentine-tolerant plants (Bakker 1984, p. 79) such as A. franciscana.
The coastal upland habitat of Arctostaphylos franciscana is
influenced by cool, humid conditions and frequent summer fog. Summer
fog is important to upland coastal vegetation and partly determines the
distribution of coastal species (Johnstone and Dawson 2010, p. 4533).
Besides serpentine soil and cool air temperatures (Parker 2010c, p. 1),
summer fog is one of the primary habitat requirements for A.
franciscana (Vasey 2010, p. 1). Summer fog results from two phenomena
upwelling of cold coastal ocean water and temperature inversion of hot
air flowing toward the ocean over a cool humid marine air layer below
(Johnstone and Dawson 2010, p. 4533; Vasey 2010, p. 1). Fog reduces
sunlight and air temperature, and raises humidity. Summer fog provides
a source of water for plants, including Arctostaphylos species, by
condensing in the plant canopy and falling directly as water to the
soil
[[Page 54437]]
where it is taken up by the plant's roots or directly by leaves
(Johnstone and Dawson 2010, p. 4533; Vasey 2010, p. 1).
Historically, the maritime serpentine chaparral plant community, of
which Arctostaphylos franciscana is a part, may have been present in
the southeastern portion of the San Francisco area (for example,
Potrero Hill and Bayview Hill), but the cumulative effects of burning
by native Americans, grazing during the Spanish/Mexican period, and
later more grazing and firewood gathering during the U.S. military
period may have converted the maritime chaparral to grassland or
depauperate coastal scrub (Chasse 2010, p. 2). Prior to 1947, A.
franciscana was known from three locations: the Masonic and Laurel Hill
Cemeteries in San Francisco's Richmond District, and Mount Davidson in
south-central San Francisco (Service 2003, pp. 16, 62, 95; Chasse et
al. 2009, p. 4). Unconfirmed sightings were also noted at a possible
fourth location near Laguna and Haight Streets (Chasse 2012, p. 1). By
1947, the Masonic and Laurel Hill Cemetery sites were removed and the
grounds were destroyed in preparation for commercial and urban
development (Chasse et al. 2009, p. 7). The Mount Davidson and Laguna
and Haight Streets locations were lost to urbanization as well. Until
October 2009, A. franciscana had not been recorded in the wild since
1947 (Chasse et al. 2009, pp. 3, 7), although no systematic surveys are
known to have taken place to search for potential remaining individuals
(Chasse 2010, p. 1).
Cultivated Arctostaphylos franciscana
Between 1930 and 1947, prior to the loss of the wild plants,
botanists collected cuttings and rooted specimens from confirmed wild
Arctostaphylos franciscana plants, possibly representing between one
and six distinct genotypes, and propagated them in botanical gardens
(Chasse et al. 2009, p. 7; Chasse 2011a, p. 1; Chasse 2011b, p. 1;
Service 2003, p. 96; Vasey 2011b, p. 2). The number of distinct
genotypes depends on whether the botanical garden specimens were
started from cuttings of the same individual (which would mean multiple
plants have identical genotypes (genetic constitutions)), or whether
each specimen originated from a separate plant (in which case they
would have different genotypes) (Chasse 2011a, p. 1; Chasse 2011b, p.
1; Vasey 2011b, pp. 2, 3).
Modern collections of this plant at East Bay Regional Park
District's Botanical Garden at Tilden Regional Park, San Francisco
Botanical Garden (formerly known as Strybing Arboretum), Rancho Santa
Ana Botanic Garden, Claremont, and University of California (UC)
Berkeley Botanical Garden include some of the original specimens from
Laurel Hill, as well as specimens propagated vegetatively after the
species was thought to be extinct in the wild (Chasse et al. 2009, pp.
6-8). Accession records for the botanical garden specimens indicate
that some specimens collected and planted prior to 1947 did not survive
and others are duplicates of original collections, leaving possibly
only two specimens confirmed to have been original plants transplanted
from Laurel Hill (Chasse 2011b, p. 1; Smisko 2012, p. 1). Further
genetic work will verify whether plants with differing morphological
features prove to be additional Arctostaphylos franciscana individuals.
Although some of the botanical garden specimens may have different
genotypes, which is generally the result of sexual reproduction
(sprouting from seed) rather than clonal reproduction (vegetative
reproduction from cuttings or plant parts other than seeds), all of the
botanical garden specimens are considered to be A. franciscana until
further genetic work can be conducted. The number of existing distinct
genotypes cannot currently be determined because a suitable genetic
sampling technique has not yet been developed (Chasse 2011a, p. 1).
Under the conservation plan for the relocated wild plant, cuttings
and rooted specimens from the wild plant are also being cultivated.
Cuttings from the plant, both nonrooted stems and layering stems (stems
that have rooted at their leaf nodes), were taken for vegetative
propagation prior to translocation of the Arctostaphylos franciscana
plant in January 2010 (Chasse et al. 2009, pp. 10-16, 40-42, Young
2010a, p. 1). This material was distributed to seven locations,
including UC Berkeley Botanic Garden, Regional Parks Botanic Garden, UC
Santa Cruz Botanical Garden, San Francisco Botanical Garden, Cal Flora
Nursery, Presidio Nursery, and the Presidio Trust Forester (Young 2011,
p. 1 of attachment 2). As of February 2012, 351 clones continue to
survive at these locations (Young 2012, p. 1). A total of 1,346 A.
franciscana seeds were collected from the plant in 2009, before it was
transplanted; an estimated 2,100 seeds were collected in July and
August 2010; and 19 seeds were collected in 2011 (Frey 2010, p. 1;
Young 2010a, p. 1; Young 2012, p. 1). The numbers of seeds collected
are estimates based on weight of seed collected (Laskowski 2012, p. 1).
No attempts have yet been made to germinate A. franciscana seeds (Young
2012, p. 1). Two rooted A. franciscana cuttings were outplanted to
managed sites at the UC Santa Cruz Arboretum in January 2011 (Kriegar
2011, unpaginated). The conservation plan calls for eventual
propagation of seeds (including any seeds collected from the soil
around the plant's original location), and for genetic testing of
resulting plants. Seeds fertilized in the wild could result from cross-
pollination from another individual Arctostaphylos franciscana or a
closely related species to produce a genetically unique individual
(Chasse et al. 2009, p. 13). Additionally, because the roots of most
Arctostaphylos individuals establish a mutually beneficial association
with mycorrhizal fungi in the soil, the conservation plan establishes
means by which the soil for propagating cuttings and seeds should be
inoculated with spores from such fungi (Chasse et al. 2009, p. 9).
Propagation of A. franciscana seed and inoculation of seeds and
cuttings by mycorrhizal fungi have not yet occurred. Soil surrounding
the wild plant has been examined for presence of a seedbank, but no A.
franciscana seeds have been found (Young 2011, p. 1; Young 2012, p. 1).
Genetics and Taxonomy
At one time Arctostaphylos franciscana and A. montana ssp. ravenii
were considered to be subspecies of A. hookeri (Hooker's manzanita).
However, recent taxonomic revisions have established A. montana ssp.
ravenii and A. franciscana as separate species. These revisions have
been based primarily on genetic comparisons, including the fact that A.
franciscana is diploid while A. montana ssp. ravenii is tetraploid
(having four sets of chromosomes, 26 chromosome pairs) (Service 2003,
p. 95; Parker et al. 2007, pp. 149, 150; Chasse et al. 2009, p. 6). The
identification of the wild plant as A. franciscana has since been
confirmed with 95 percent confidence based on morphological
characteristics (Chasse et al. 2009, pp. 3, 4; Vasey and Parker 2010,
pp. 1, 5). Additional tests indicate that the plant is diploid,
consistent with A. franciscana (Vasey and Parker 2010, p. 6). Molecular
genetic data also indicate that the plant is A. franciscana (Parker
2010a). Based on the best available scientific information, we consider
the individual found along Doyle Drive in October 2009 to be A.
franciscana (Vasey and Parker 2010, pp. 1, 5-7).
[[Page 54438]]
Previous Federal Actions
Arctostaphylos franciscana was originally proposed for listing as
an endangered species under the Act in 1976 (41 FR 24524; June 16,
1976). In 1980, it was included in the list of Category 1 candidates
for listing as one of the taxa retaining a high priority for addition
to the list, subject to confirmation of extant wild populations. At
that time, the species was thought to be extinct in the wild, although
it was known to be extant in cultivation (45 FR 82479; December 15,
1980). It was included as a species of concern in the Recovery Plan for
Coastal Plants of the Northern San Francisco Peninsula (Service 2003,
pp. 95-96).
On December 23, 2009, we received a petition dated December 14,
2009, from Wild Equity Institute, Center for Biological Diversity, and
California Native Plant Society requesting that Arctostaphylos
franciscana be listed as endangered on an emergency basis under the Act
and that critical habitat be designated. Included in the petition was
supporting information regarding the species' taxonomy and ecology,
historical and current distribution, present status, and actual and
potential causes of decline. On January 26, 2010, we acknowledged the
receipt of the petition in a letter to Wild Equity Institute. In that
letter, we responded that we had reviewed the information presented in
the petition and determined that issuing an emergency rule to
temporarily list the species, under section 4(b)(7) of the Act, was not
warranted. Our rationale for this determination was that, although only
a single plant of this species remained in the wild, the individual had
recently been transplanted to a new location on Federal land.
Additionally, a conservation plan (Chasse et al. 2009, pp. 1-44) and
associated MOA (cited herein as Caltrans et al. 2009) signed by five
Federal and State wildlife and land management agencies (conservation
partners) successfully addressed the concerns raised by the petition to
the extent that none of those concerns constituted an ``emergency
posing a significant risk to the well-being of the species'' (50 CFR
424.20(a)). The Federal agencies participating in the MOA are the NPS
and the Service. The State of California is represented by Caltrans and
the California Department of Fish and Game (CDFG). The Presidio Trust,
a wholly owned government corporation that jointly manages the Presidio
with NPS, also participates (71 FR 10608; March 2, 2006).
The transplanted plant is considered to be the single remaining
plant in the wild, despite having been transplanted to the Presidio.
The original habitat of the plant was threatened by the ongoing
redevelopment of Doyle Drive, but that threat was removed by moving the
plant to a new location (translocation). Potential immediate threats in
the new location, including the danger that the plant might not survive
the move and transplantation, were addressed by provisions in the
conservation plan for collecting and propagating rooted clones, seeds,
and cuttings from the original plant prior to translocation. The
conservation plan provides for the long-term propagation, and eventual
reestablishment in wild populations, of all remaining genetic lines,
including those from the surviving wild plant and from the individuals
located in two botanical gardens, which were collected from
historically confirmed locations. It also includes long-term monitoring
provisions. While these provisions do not remove the need for further
review of the species' status, they appear to be effective for
protecting the species in the short term.
We published a 90-day finding in the Federal Register on August 10,
2010 (75 FR 48294), in which we found that the petition presented
substantial scientific or commercial information indicating that
listing this species may be warranted. On June 14, 2011, Wild Equity
Institute filed a complaint that alleged that, given our 90-day
finding, the Service had failed to make the required 12-month finding
on the petition in a timely manner. On September 8, 2011, we published
a combined 12-month finding and proposed rule in the Federal Register
in which we determined that listing Arctostaphylos franciscana was
warranted, and, as a result, we proposed to list the species as
endangered (76 FR 55623). We also stated that we did not find critical
habitat to be determinable at that time, and requested information and
comments on whether designation of critical habitat for the species was
prudent and determinable.
The Presidio is under joint management by the Golden Gate National
Recreation Area (GGNRA), a part of NPS, and the Presidio Trust. The
wild Arctostaphylos franciscana plant is located in the portion of the
Presidio managed by the Presidio Trust. The plant is considered to be
wild because it has been moved to an undeveloped area of the Presidio
that is managed as natural habitat. Although the plant is currently
receiving care (monitoring and insect removal) associated with its
transplantation and recent infestation by insects, it is not receiving
the level of protection, water, or nutrients given to the plants in
botanical gardens or to those within the nursery trade.
Summary of Comments and Recommendations
In the proposed rule published on September 8, 2011 (76 FR 55623),
we requested that all interested parties submit written comments on the
proposal by November 7, 2011. We also contacted appropriate Federal and
State agencies, scientific experts and organizations, and other
interested parties and invited them to comment on the proposal. A
newspaper notice inviting general public comment for a period of 15
days was published in the San Francisco Chronicle on June 5, 2012. A
question and answer sheet and news release regarding the species was
posted online on our Web site for the public. We did not receive any
requests for a public hearing.
During the comment periods for the proposed rule, we received eight
comment letters directly addressing the proposed listing of
Arctostaphylos franciscana as endangered. All public commenters
supported listing the species as endangered. Three commenters supported
designation of critical habitat and provided opinions on the value of
critical habitat designation and the threats resulting from lack of
this designation. One commenter opposed critical habitat designation.
All substantive information provided during the comment periods has
either been incorporated directly into this final determination or is
addressed below.
Peer Review
In accordance with our peer review policy published on July 1, 1994
(59 FR 34270), we solicited expert opinion from five knowledgeable
individuals with scientific expertise that included familiarity with
Arctostaphylos franciscana and its habitat, biological needs, and
threats. We received responses from four of the peer reviewers.
We reviewed all comments received from the peer reviewers for
substantive issues and new information regarding the listing and
critical habitat of Arctostaphylos franciscana. The peer reviewers
generally concurred with our methods and conclusions regarding listing
and provided additional information, clarifications, and suggestions to
improve the final rule; however, three reviewers disagreed with our
comments that designation of critical habitat was not prudent or
determinable, and they provided supporting information regarding
critical habitat. The fourth peer reviewer
[[Page 54439]]
indicated that publicizing the location of the transplanted plant could
increase the threat of infection by Phytophthora species. Additionally,
this peer reviewer noted that the threat to A. franciscana was greater
than stated in the proposed rule due to the presence of other species
of Phytophthora in the San Francisco Bay area. Peer reviewer comments
are addressed in the following summary and incorporated into the final
listing rule as appropriate. A proposed rule to designate critical
habitat for A. franciscana is published in the Proposed Rules section
of today's Federal Register. Please see that proposed rule for
information on submitting a comment on our proposed designation of
critical habitat for A. franciscana.
Peer Reviewer Comments
(1) Comment: All peer reviewers provided comments on conservation
measures, recommendations for outplanting cuttings and selection of
planting sites, and additional information on threats to the species
from the five factors discussed below in Summary of Factors Affecting
the Species.
Our Response: Recommendations regarding outplanting and selection
of planting sites have been reviewed for the proposed critical habitat
and will be considered during the development of a recovery plan. All
other appropriate information was incorporated into this final rule.
(2) Comment: Three peer reviewers and three public commenters
stated that designation of critical habitat is prudent and
determinable.
Our Response: Critical habitat is defined in section 3 of the Act
as: (1) The specific areas within the geographical area occupied by the
species, at the time it is listed in accordance with the Act, on which
are found those physical or biological features that are essential to
the conservation of the species, and which may require special
management considerations or protection; and (2) specific areas outside
the geographical area occupied by the species at the time it is listed,
upon a determination that such areas are essential for the conservation
of the species. The peer reviewers provided information on the
ecological requirements of Arctostaphylos franciscana and areas with
the highest potential for establishing new populations. Based on this
information, we have determined that the designation of critical
habitat is prudent and determinable. All known remaining historic
locations as well as the site of the transplanted wild plant have been
evaluated, and the areas that have met our criteria to be included as
proposed critical habitat have been identified. We are proposing to
designate critical habitat for the species concurrently with this final
rule. That proposal is published in the Proposed Rules section of
today's Federal Register. Please see that proposed rule for information
on submitting a comment on our proposed designation of critical habitat
for A. franciscana.
(3) Comment: Two peer reviewers disagreed with our statement that
small sites on the order of 0.4 hectare (ha) (1 acre (ac)) may not be
suitable for Arctostaphylos franciscana. One peer reviewer stated that
while small sites may facilitate the growth of nonnative plant species,
A. franciscana would be started from cuttings, not from seed, and
management efforts could easily accommodate competition from nonnative
plants, as established woody species are not easily displaced by weeds.
The second peer reviewer noted that there are many natural occurrences
of rare Arctostaphylos species existing in small, isolated remnants of
habitat where soils and climate are suitable.
Our Response: Some invasive plant species in the Presidio and in
other San Francisco peninsula areas have been shown to be difficult to
control. For example, on Mount Davidson, which previously supported a
population of Arctostaphylos franciscana, invasive plant species,
including Eucalyptus spp., invasive ivy, and other species, have
largely displaced native vegetation on portions of the site. We agree
that some rare species of Arctostaphylos have persisted on small
parcels of suitable habitat; however, in order to maximize the
potential of establishing multiple, successful populations of A.
franciscana, selection of suitable sites that require the least amount
of long-term maintenance and promise the greatest opportunity for
growth is necessary. However, we will evaluate small sites during our
process to designate critical habitat for the species.
(4) Comment: Two peer reviewers questioned our statement under
Factor A in the proposed rule that small, isolated areas of habitat can
be drier than larger ones due to evaporation and lack of surrounding
vegetation. One reviewer stated that this does not apply to small urban
or near-urban sites because hard surfaces such as asphalt and cement
provide additional runoff and available moisture in these areas.
Our Response: Many of the remnant parcels of potential habitat on
the peninsula are isolated and surrounded by urban development or
nonnative landscaping rather than native vegetation. One of the general
effects of this abrupt transition from natural habitat to urban
landscape or hard surfaces is a change in the abundance and
distribution of species in the natural habitat due to physical
conditions near the edge (the edge effect). These conditions include
desiccation and changes in wind and light. We agree with one peer
reviewer's premise that hard surfaces such as rooftops, streets, and
parking lots increase urban runoff; however, our understanding is that
when rain or irrigation water falls on urban hard surfaces, it flows
predominately into storm water control systems, including gutters and
storm drains, and is carried away from urban areas rather than being
absorbed into the soil and providing more moisture to plants.
(5) Comment: We stated under Factor A that remaining areas of
greenstone and serpentine habitat on the peninsula are frequently 0.4
ha (1 ac) or less in size and may no longer be appropriate sites for
re-establishment of Arctostaphylos franciscana due to fragmentation and
loss of native plant diversity in the small remnant areas. One peer
reviewer pointed out the loss of native diversity in existing stands of
vegetation is not a relevant argument because new populations of A.
franciscana would be newly created in the small sites.
Our Response: We appreciate the reviewer's point and agree that if
small remnant habitat areas were to support Arctostaphylos franciscana,
it would be through restoration with newly assembled populations of the
species, which could permit establishment of other naturally co-
occurring natives. However, we remain concerned that small sites may
insufficiently support the pollinator, fruit-dispersal, and mycorrhizal
communities that are thought to contribute to successful establishment
of the species. We will be looking at all potential sites when
selecting locations for outplanting.
(6) Comment: One peer reviewer noted that the threat to
Arctostaphylos franciscana from nonnative, root-rotting Phytophthora
species is greater than noted under Factor C in the proposed rule. He
noted that species of Phytophthora differ in their ecological
requirements, such as optimum temperature range. Several species of
Phytophthora have become established in a variety of San Francisco Bay
area microclimates and could be introduced to the vicinity of A.
franciscana. He also noted that other factors discussed under Factor E,
including climate change, soil compaction, and low genetic diversity,
have the potential to increase the risk to
[[Page 54440]]
the existing wild plant from P. cinnamomi and other Phytophthora
species.
Our Response: This information has been incorporated into this
final rule. Please see Factor C discussion on threats to Arctostaphylos
franciscana associated with disease below.
(7) Comment: One peer reviewer noted that the general strategy to
recover Arctostaphylos franciscana should be two-fold: (A) Identify
other genotypes of A. franciscana that have been cultivated in
botanical gardens and use their cuttings to propagate large numbers of
plants for future outplantings in restored habitats, and (B) identify
and secure sites for outplanting these clones and create as many
populations within the historical range as feasible.
Our Response: This information has been incorporated into this
final rule where appropriate and will be considered during development
of the proposed critical habitat and recovery actions for the species.
(8) Comment: One peer reviewer noted that the potential risks of
failure of small, restored populations are outweighed by benefits of
having a large number of isolated populations within the range of
Arctostaphylos franciscana. These populations would buffer the wild A.
franciscana from the threats noted in this rule, including disease,
disturbance, predation, and climate change. The peer reviewer further
noted that having many scattered populations will optimize the
potential for at least some populations to adjust to climate change.
Our Response: We concur with this opinion and are considering this
during our development of proposed critical habitat and recovery
actions for the species.
Comments from States
Section 4(i) of the Act states, ``the Secretary shall submit to the
State agency a written justification for his failure to adopt
regulations consistent with the agency's comments or petition.'' No
comments were received from the State regarding the proposal to list
Arctostaphylos franciscana as an endangered species.
Federal Agency Comments
No comments were received from any Federal agencies.
Public Comments
(9) Comment: All seven commenters noted that the species should be
listed and protected in the wild because only one plant is known to
exist.
Our Response: Comments noted.
(10) Comment: One commenter noted that not all nursery stock of
Arctostaphylos franciscana is of unknown origin. The commenter stated
that UC Berkeley Arboretum and Yerba Buena Nursery sell plants of known
origin. Plants from Yerba Buena Nursery have been planted in Golden
Gate Park Arboretum, which validates their legitimacy. The commenter
further stated that specimens from verified sources are a vital
repository and should not be disregarded.
Our Response: The UC Berkeley Botanical Garden does not sell
Arctostaphylos franciscana plants; however, their stock was originally
from the Laurel Hill Cemetery and may have been the source for plants
sold by California Native Plant Society (Forbes 2012, p. 1). We agree
that some A. franciscana plants in the nursery trade originated from
plants salvaged from the Laurel Hill Cemetery prior to its destruction
in 1947; however, it is difficult to trace the lineage of all nursery
plants in the intervening 65 years. Some currently available, nursery-
grown A. franciscana plants could be cultivars selected for specific
growth characteristics, and others could be the product of hybrid seed.
Plants from Yerba Buena Nursery that were planted at Golden Gate Park
Arboretum, now known as the San Francisco Botanic Garden, are believed
to be A. franciscana (D. Mahoney 2012, pers. comm.). We encourage the
use of plants that are proven to be A. franciscana to generate stock
for additional populations of A. franciscana. However, introgression
(the spread of genes of one species into the gene pool of another by
hybridization) could occur if hybrid nursery stock is outplanted near
the wild plant and cross-fertilization occurs. Because of the
uncertainty of the origin or subsequent hybridization, we currently
only consider the plants of confirmed origin at East Bay Regional Parks
Botanic Garden at Tilden Regional Park and at UC Botanical Garden at
Berkeley, and the wild plant on the Presidio to be A. franciscana and
the listed entity.
(11) Comment: One commenter noted that there is no apparent
incentive for anyone to poach or vandalize plants in natural settings
that are available in the nursery trade.
Our Response: Plants have been vandalized in Golden Gate Park,
including species that are also available in nurseries such as elm and
sycamore trees, and rose bushes (King 2010, unpaginated; Gordon 2010,
unpaginated). The fact that a plant is available in the nursery trade
does not protect it from being vandalized or poached.
(12) Comment: A commenter noted that leaving the nursery trade
specimens of Arctostaphylos franciscana unlisted may result in
introgression. The commenter suggests that including nursery stock in
the listed entity will help to regulate this threat.
Our Response: Arctostaphylos franciscana has been available to the
public in the nursery trade for many years, and introgression of this
species with other manzanitas may have already occurred. Including A.
franciscana nursery stock as part of the listed entity will have no
effect on controlling hybridization of these plants. Only the removal
of A. franciscana from nursery production could minimize its
hybridization with other species of Arctostaphylos while in the nursery
setting.
(13) Comment: A commenter noted that if the Arctostaphylos
franciscana plants in the nursery trade are not considered to be the
listed species, they should be protected under the similarity of
appearance provisions of the Act.
Our Response: We acknowledge that similarity of appearance is a
tool available to us under the Act. Section 4(e) of the Act states that
the Secretary may treat any species as an endangered species or
threatened species even though it is not listed pursuant to section 4
of the Act if he finds that: (1) Such species so closely resembles in
appearance, at the point in question, a species which has been listed
that enforcement personnel would have substantial difficulty in
attempting to differentiate between the listed and unlisted species;
(2) the effect of this substantial difficulty is an additional threat
to an endangered or threatened species; and (3) such treatment of an
unlisted species will substantially facilitate the enforcement and
further the policy of the Act. It should be noted, however, that the
basic intent of section 4(e) of the Act is to prevent the inadvertent
harm to the listed species in the wild resulting from its similarity to
a different species that is not protected by the Act. The
Arctostaphylos franciscana plants in the nursery trade do not need the
protection of the Act, and including them in this listing under section
4(e) will provide no or minimal benefit to the wild specimen or any
future outplantings of the listed entity. Similarity of appearance
protections can be effective in situations where collection of a
species is highly desirable (such as for insects or butterflies) and
such collection is the primary threat or a threat of such an extent
that not including the similar
[[Page 54441]]
species with the listed entity would greatly affect the listed species'
status. Although collection of the remaining wild plant and any future
outplantings is a potential threat, no known collection has occurred to
date, and we would not consider this threat to be of such a high level
as to greatly affect the species' status. As a result, we have
determined that treating A. franciscana plants in the nursery trade as
endangered under section 4(e) of the Act would not substantially
facilitate enforcement or the policy of the Act, and the Secretary is
not invoking section 4(e) of the Act for A. franciscana.
(14) Comment: One commenter disagreed with information we reported,
which indicated that lands in Area B of the Presidio, which are managed
by the Presidio Trust, could be dispersed to the private sector and
become available for development if the Presidio Trust is not
financially self-sufficient by 2013. Further, the commenter does not
agree that differences in the missions of the Presidio Trust and NPS
would cause uncertainty in the future management of the Arctostaphylos
franciscana and its habitat.
Our Response: The Presidio Trust Act of 1996 states in section
105(b) that the Presidio Trust must be self-sufficient within 15
complete fiscal years of the first meeting of the Presidio Board of
Directors, thereby requiring that the Trust be self-sufficient by 2013
(Presidio Trust Act, p. 9; Presidio Trust Management Plan 2002, p. 1).
Because this timeframe extends into the future, there is no assurance
that this goal will be met. The Presidio Trust, as stated in the
Presidio Trust Management Plan (2002, pp. 1, 12), is directed to
preserve natural, scenic, cultural, and recreation resources, and at
the same time ensure that the Presidio becomes financially self-
sufficient. Again, as stated in the Presidio Trust Management Plan
(2002, pp. 1, 12), ``Congress gave the Trust the authority to lease
property and generate revenues, and required the Presidio to be
financially self-sufficient by 2013. Once appropriations cease, the
Trust must use the park's building assets to fund its rehabilitation
and to pay for its ongoing operation. No other area within the National
Park System is managed in the same way or operates under the same
financial requirement.'' The mission of NPS on the Presidio, as stated
in the Golden Gate National Recreation Area Addition Act of 1992 (16
U.S.C. 460bb), while similar to the Presidio Trust Act in protecting
values and resources, does not include the mandate that the public
lands under NPS authority become financially self-sufficient.
(15) Comment: One commenter stated that there are no remaining
landfill remediation sites on the Presidio that have the potential to
impact Arctostaphylos franciscana, and that all waste material has been
removed from the landfill remediation site closest to where the wild
plant is located. The commenter noted that this work was completed
without impacts to A. franciscana and asked that we delete the text
under Factor A that refers to the Presidio Environmental Remediation
Program.
Our Response: Remediation of the landfill site closest to the
Arctostaphylos franciscana on the Presidio is being completed without
apparent impact to the wild plant, and no further remediation projects
are located within the vicinity of the plant. Remediation of this
landfill site has been deleted as a current threat from the Factor A
discussion.
(16) Comment: A commenter noted that under Factor E we stated that
the Arctostaphylos franciscana plant is located near an area available
for public events and threatened by foot traffic. The commenter stated
that this area is available one afternoon per week for wedding
ceremonies and does not present a threat to the plant, and requested
that reference to this event space be removed as a threat.
Our Response: As stated in the proposed rule, the Presidio is a
highly popular, easily accessible National Park contiguous with the
City of San Francisco, which receives 5 million visitors each year. The
public area described in the proposed rule, which is available for
public events, provides views of the San Francisco Bay and the City of
San Francisco, and attracts a large number of visitors year round. The
best information available to us indicates that the public has
unrestricted access to this area 24 hours a day, every day of the year;
therefore, this site may be a different location than that referred to
by the commenter. Additionally, the Arctostaphylos franciscana plant
has been located near common-use trails with unrestricted access.
Because of its proximity to these heavily used areas, the plant could
be damaged accidentally or intentionally by park users. The Presidio
Trust and NPS are concerned that authorized and unauthorized group
tours by plant enthusiasts could overwhelm the plant and compact the
soil (T. Thomas, pers. comm., 2011).
(17) Comment: One public commenter stated that designation of
critical habitat is not prudent or determinable for the reasons stated
in the proposed rule.
Our Response: As noted in our response to comment 2, the peer
reviewers provided information on the ecological requirements of
Arctostaphylos franciscana and areas with the highest potential for
establishing new populations. Based on this information, we have
determined that the designation of critical habitat is prudent and
determinable. As a result, a proposed rule to designate critical
habitat for A. franciscana is published in the Proposed Rules section
of today's Federal Register. Please see that proposed rule for
information on submitting a comment on our proposed designation of
critical habitat for A. franciscana.
Summary of Changes From Proposed Rule
Based on peer review and public comments (see comments 1, 6, 7, and
15 in the Summary of Comments and Recommendations section above), and
monitoring of the wild plant, we have added new information in the
Species Information section and additional threats information in the
Summary of Factors Affecting the Species section to better characterize
our knowledge of the species' habitat requirements and threats. After
input from peer reviewers and public comment, we have determined that
the designation of critical habitat is prudent and determinable, and we
are proposing to designate critical habitat, as described in a separate
proposed critical habitat rule in today's Federal Register.
Summary of Factors Affecting the Species
Section 4 of the Act and its implementing regulations (50 CFR part
424) set forth the procedures for adding species to the Federal Lists
of Endangered and Threatened Wildlife and Plants. A species may be
determined to be an endangered or threatened species due to one or more
of the five factors described in section 4(a)(1) of the Act: (A) The
present or threatened destruction, modification, or curtailment of its
habitat or range; (B) overutilization for commercial, recreational,
scientific, or educational purposes; (C) disease or predation; (D) the
inadequacy of existing regulatory mechanisms; or (E) other natural or
manmade factors affecting its continued existence. Listing actions may
be warranted based on any of the above threat factors, singly or in
combination. Each of these factors is discussed below.
[[Page 54442]]
A. The Present or Threatened Destruction, Modification, or Curtailment
of Its Habitat or Range
All areas of habitat originally known to be occupied by
Arctostaphylos franciscana have been lost to urban development or to
habitat conversion through the introduction of nonnative plant species
(Chasse et al. 2009, pp. 4, 7; Chasse 2011c, p. 1). The largest
historical occurrence was at the quarry area of the former Laurel Hill
Cemetery in San Francisco (Chasse 2011c, p. 1). Most of this area was
converted to residential housing and city streets after the late 1940s.
A small remaining area of open space at Laurel Hill is dominated by
ornamental shrubs and invasive understory plants, although serpentine
rock is visible in several openings (Chasse 2011c, p. 1). Lawns,
pathways, and buildings, part of the University of San Francisco
campus, now occupy the location of the Masonic Cemetery occurrence
(Chasse 2011c, p. 2). The precise location of the third historical
occurrence of A. franciscana, at Mount Davidson, is unknown but thought
to be on one of the greenstone outcrops (Chasse 2011c, p. 2). The upper
portions of Mount Davidson are covered with nonnative trees and
invasive understory species; some grassland and scrub persist on the
south and northeast sides (Chasse 2011c, p. 2). The species' range is
now limited to the single transplanted location on the Presidio. In
January 2010, after the newly discovered wild plant was moved to the
Presidio, the plant's habitat at Doyle Drive was destroyed as part of a
Caltrans highway improvement project.
Past urban development on the San Francisco peninsula has limited
the remaining areas of potential habitat for Arctostaphylos franciscana
by habitat conversion and habitat degradation and, to a lesser degree,
habitat fragmentation. Some of these small remnant areas may no longer
be suitable for reestablishment of A. franciscana due to factors such
as dominance by other plant species (Chasse pers. comm., 2011).
Currently, these small, isolated parcels are subject to edge effects,
such as changes in soil moisture, changes in light, and potential
increased invasion of weed species that would compete with A.
franciscana for limited resources (water, nutrients, space).
Urban barriers, such as streets and buildings, have been found to
impose a high degree of isolation on chaparral species and, over time,
to result in decreased numbers of native plant species and concurrent
increased numbers of nonnative plant species in the habitat fragments
(Alberts et al. (unpubl.) as cited in Soule et al. 1992, p. 41; Soule
et al. 1992, pp. 41-43). These effects of urbanization on the San
Francisco peninsula are expected to continue to affect these remnant
parcels into the future, and to pose a threat to the establishment of
additional Arctostaphylos franciscana plants, without assistance to
restore suitable habitat conditions and to restore plants to suitable
locations.
Additionally, nitrogen deposition may modify habitat by increasing
soil nutrients, thus posing a current and continuing threat to remnant
habitat that might otherwise be suitable for Arctostaphylos
franciscana. Weiss and Luth (2003, p. 1) have conducted research on the
effects of nitrogen deposition in a serpentine grassland south of the
San Franciscan peninsula. They found that nitrogen deposition from
automobiles on Highway 280 (a north-south oriented highway on the
peninsula) was responsible for higher nitrogen levels in the soil
within 400 m (1,312 ft) on the west side and 100 m (328 ft) on the east
side of the roadway. Nitrogen deposition was correlated with increased
nonnative grass cover in these areas, resulting in competition for
space for native plants. Native species within this zone are thought to
be at long-term risk from invasions of nitrogen-loving grasses and
other weedy plant species (Weiss and Luth 2003, p. 1). An increase in
nonnative grass cover through changed habitat conditions could threaten
the wild A. franciscana by competing for soil moisture and nutrients
and could inhibit successful germination of A. franciscana seed. The
entire northern San Francisco peninsula, with the exception of the
Presidio and Golden Gate Park, has been urbanized, and four major
highways (Highways 1, 101, 280, and 480) and other urban roadways
dissect the peninsula. Urban areas and roadways are a continuous source
of nitrogen deposition from automobiles, trucks, and industrial and
home heating (Weiss 1999, p. 1477). Invasions of nitrogen-loving plants
into nitrogen-limited grasslands and shrublands appears to be a common
response to atmospheric nitrogen deposition (Weiss and Luth 2003, p.
1), and may partly explain why the ecosystem that existed on the San
Francisco peninsula has been so altered.
The one remaining wild Arctostaphylos franciscana plant is subject
to multiple threats. The Presidio Trust Act contains a sunset clause
that could result in the transfer of Presidio holdings to the General
Services Administration (GSA) for disbursement if the Presidio Trust
operations are not self-sufficient by 2013 (the Presidio Trust Act is
discussed under Factor D below). In the unlikely event that the
Presidio Trust is not self-sufficient within that timeframe, the
potential that lands could be transferred and become available for
development presents a threat of additional habitat loss in the future.
Based on the best scientific and commercial information available,
we consider the present or threatened destruction, modification, or
curtailment of the species' habitat or range to be a high-magnitude and
ongoing threat to the wild population of Arctostaphylos franciscana.
The current fragmented and degraded condition of most remaining
serpentine or greenstone soil habitat on the San Francisco peninsula
threatens the ability of Arctostaphylos franciscana to expand its
range. The threats of possible development and change in management of
the habitat may further limit the species' propagation and expansion,
and could potentially threaten the only remaining wild plant. The loss
of the plant's native serpentine chaparral habitat to development and
the curtailment of its range restrict the species' current and future
ability to naturally reproduce and expand its range.
B. Overutilization for Commercial, Recreational, Scientific, or
Educational Purposes
Overutilization of Arctostaphylos franciscana is possible due to
its popularity for landscape use, as evidenced by the widespread use of
cultivars of this species in the commercial nursery trade.
Arctostaphylos franciscana is specifically recommended for use in
erosion control on steep slopes (Theodore Payne Foundation 2009, p. 1;
Sierra Club 2011, p. 1).
The attention and media coverage generated by the discovery of a
species thought to be extirpated from the wild may result in efforts by
the public to visit the plant and possibly collect cuttings or seed.
Although the location of the transplanted plant has not been disclosed,
it was planted in a heavily used area in the Presidio, near common-use
trails with unrestricted access by the public. The Presidio is a
National Park and is part of the GGNRA; it is open to the public 24
hours a day, every day of the week and receives 5 million visitors
annually. The Presidio receives heavy use because of its proximity to
the City of San Francisco, and because the National Park has no
entrance fees and contains restaurants, trails, and businesses that can
be accessed by car, foot, or public transport. The Presidio
[[Page 54443]]
Trust and NPS are making serious efforts to avoid disclosing the
location of the translocated plant. The Presidio Trust and NPS are
concerned that public knowledge of the plant's location would lead to
authorized and unauthorized group tours by plant enthusiasts (T.
Thomas, pers. comm., 2011).
No damage to the plant has been observed to date; however,
trampling or the taking of cuttings could occur if the identification
and location of the plant becomes known. Similarly, another extremely
rare plant, Arctostaphylos montana ssp. ravenii, is also located on the
Presidio. Although it was federally listed in 1979, its location has
not been revealed to the public by the Presidio Trust or NPS in order
to protect the plant from vandalism. There has been no evidence of
cuttings being taken from A. franciscana or the similar A. montana ssp.
ravenii (Chasse 2011c, p. 3); however, the fact that the sole remaining
wild A. franciscana is located in a heavily used public area subjects
this species to the threat of collection.
Based on the best scientific and commercial information available,
we consider overutilization for commercial and recreational purposes to
be a threat to the wild Arctostaphylos franciscana plant. Although
nursery-grown A. franciscana are available to residents for use in
private gardens, collection of the wild plant is a threat to the
species, and we expect it may be a threat in the future, particularly
if the location of the plant becomes known to the public.
C. Disease or Predation
Disease
Transplantation of the single wild Arctostaphylos franciscana plant
may have caused stress to the plant, and thereby made it more
susceptible to predation and disease. In transplanted plants, stress
and root damage may occur from a variety of factors, including soil
compaction from foot traffic around the plant (Hammitt and Cole 1998,
p. 52), too little or too much water, and improper planting depth;
these stressors may result in increased susceptibility to disease (see
further discussion in Visitor Use section below). A fungal infection
called twig blight, usually caused by Botryosphaeria species in
Arctostaphylos, is also a potential concern, particularly during wet
years (Service 2003, p. 69). Twig blight was observed in the wild plant
during the winter of 2009-2010, but it subsided during the dry summer
months (Chasse 2010, p. 2). These fungi can cause both twig blighting
and perennial branch cankers that can eventually kill large branches
(Swiecki 2011, p. 1). While these pathogens would not likely pose a
serious threat to a large population, they could threaten A.
franciscana because the wild population is limited to a single plant,
and infection by this group of fungi is one of the major factors
leading to the decline of older Arctostaphylos sp. plants (Swiecki
2011, p. 1). Additionally, cankers caused by Botryosphaeria are more
severe in plants that are stressed by lack of water. The transplanted
plant may have experienced water stress due to loss of roots during the
transplanting process (Swiecki 2011, p. 1).
Arctostaphylos franciscana is also threatened by various pathogens
in the genus Phytophthora. An oak tree infected with sudden oak death
disease was discovered on the Presidio in 2010 (Fimrite 2011). Sudden
oak death is caused by Phytophthora ramorum. Phytophthora is a fungus-
like organism most closely related to diatoms and kelp (Kingdom
Stramenopila) rather than to the true fungi (Kingdom Fungi or
Eumycota). Phytophthora ramorum has so far been observed to cause only
a foliar blight in species of Arctostaphylos, rather than the lethal
bark cankers that occur on members of the black oak group (Swiecki
2012a, p. 1). However, a related species, P. cinnamomi has presented a
serious threat to other Arctostaphylos species and is expected to be a
serious threat to A. franciscana. Phytophthora cinnamomi, a soil-borne
pathogen, has long been known as a world-wide threat to commercial and
ornamental plants. It is an introduced exotic pathogen in North
America; its native range is unknown, but is suspected to be southeast
Asia. Human-related activities, including the international plant
trade, have facilitated the spread of P. cinnamomi into many habitats
worldwide (Swiecki et al. in press, p. 3). Phytophthora cinnamomi was
introduced to California early in the 20th century, and recently has
been identified as a serious threat to the State's native plants and
their habitats (Swiecki et al. in press, p. 3).
Phytophthora cinnamomi has been the cause of the decline and death
of rare Arctostaphylos species, including the federally threatened A.
pallida (pallid manzanita) in the Oakland Hills of the East San
Francisco Bay region and the federally threatened A. myrtifolia (Ione
manzanita) near Ione in the Sierra Nevada foothills of Amador County.
The pathogen is also noted in the decline of other woody native species
in the San Francisco Bay area (Swiecki et al. in press, pp. 3-5). The
organism causes root decay but can also kill above-ground portions of
some plants (Swiecki et al. in press, p. 3). Phytophthora cinnamomi is
persistent in soil, and once introduced to native habitat it cannot be
eradicated (Swiecki et al. in press, p. 3). Phytophthora cinnamomi is
transmitted by contaminated shoes, tools, and infested soil clinging to
tires, and by contaminated nursery stock, including native plant stock.
Many areas showing plant mortality caused by P. cinnamomi are
associated with hiking trails, landscapes with ornamental plants, and,
in one case at the Apricum Hill Preserve in Amador County, California,
use by visitors, including researchers, agency personnel, students, and
the general public (Swiecki et al. in press, p. 4).
Phytophthora cinnamomi poses a significant current and future
threat to Arctostaphylos franciscana because of the potential for
infestation caused by the public and staff who regularly work with the
plant. It is not possible to predict if or when the pathogen might
infect the wild plant because the disease is generally transmitted
directly or indirectly by humans or human activity. The pathogen could
be introduced from soil on contaminated shoes and tools, or from
cuttings of A. franciscana plants currently grown in a number of San
Francisco Bay area nurseries that could become contaminated. Swiecki et
al. (in press, p. 6) tested A. menziesii plants purchased from four
nurseries and found them to be infested with four Phytophthora species
that cause root infections or stem cankers, including P. cinnamomi.
Crown rot, which is caused by P. cinnamomi, is known to occur in A.
myrtifolia and A. viscida (Swiecki et al. in press, p. 3), and is a
concern when outplanting nursery-grown plants to wild locations (Chasse
et al. 2009, p. 17). However, crown rot has not been observed in the
wild A. franciscana plant (Chasse 2010, p. 2).
Conservation proposals include recommendations that Arctostaphylos
franciscana cuttings be planted with the transplanted A. franciscana to
facilitate cross-pollination of the different genotypes. Should the
wild plant become contaminated with P. cinnamomi, the result would be
the decline and death of the wild plant and permanent contamination of
the soil and seedbank beneath the plant. Any seedlings that germinate
from this seedbank would also very likely be contaminated and not
survive. Any cuttings that become contaminated are also expected to die
of the pathogen. The Golden Gate National Parks Conservancy Nurseries
staff in charge of propagation and care of A. franciscana
[[Page 54444]]
cuttings are aware of the threat of contamination and rigorously follow
clean procedures to prevent infection to the cuttings or the wild
plant; however, a risk of contamination continues to exist because
current fungicides do not eradicate 100 percent of Phytophthora spores
(Young 2010b, p. 1). The cuttings and layers from the single wild plant
have been dispersed to seven different locations and growers, which,
while decreasing the risk of complete loss of plant material, also
increases the risk of exposure to disease.
Phytophthora cinnamomi is not the only introduced soil-borne
Phytophthora species that may threaten Arctostaphylos franciscana.
Swiecki (2011, p. 1; 2012b, p. 1) notes that at least five other
species of Phytophthora associated with the decline and death of woody
plants have been found in the Crystal Springs watershed 27 to 40
kilometers (km) (17 to 25 miles (mi)) south of the Presidio. These
nonnative Phytophthora species include P. cambivora, P. cactorum, and
P. megasperma; all are known to occur in natural and cultivated
landscapes and are common in nursery stock (Swiecki 2011, p. 1).
Phytophthora cinnamomi and P. cambivora have been detected in China
Camp State Park, 22.4 km (14 mi) north of the Presidio, and P.
cinnamomi has been found in the East Bay area 24 km (15 mi) east of the
Presidio. Because several of these soil-borne pathogens have become
established in the San Francisco Bay area, the likelihood is increased
that one or more could be introduced to the vicinity of the wild
Arctostaphylos franciscana plant (Swiecki 2011, p. 1).
Predation
After being transplanted, the wild plant became severely infested
with the larvae of a native leaf roller moth (Argyrotaenia franciscana)
(Estelle 2010, p. 1). Treatment for the infestation was hand removal of
the larvae and all infected leaves, which resulted in the removal of
some of the new growth on the plant (Estelle 2010, p. 1; Young 2010a,
p. 1). A parasitic wasp emerged from one captured leaf roller moth
larva, indicating that the moth has natural enemies (Frey 2010, p. 2).
The moth has not been known to kill plants and does not appear to be a
serious threat at this time; however, the moth species was found to
have five overlapping generations in a year (Estelle 2010, p. 1).
Monthly removal of moth larvae and pupae is conducted as needed
(Estelle 2012a, p. 1). The leaf roller moth infestation in early 2010
did not permanently damage the plant, and new growth was observed (Frey
2010, p. 2). Fewer leaf roller moth larvae were seen on the wild plant
in 2011 than in 2010 (Estelle 2012a, p. 1).
Damage to Arctostaphylos franciscana branches by California voles
has been observed by Presidio Trust staff (Chasse 2011c, p. 2). Several
voles have been observed in and around the wild A. franciscana plant,
and some branch dieback has been attributed to gnawing by voles and
other rodents (Chasse 2011c, p. 2).
Based on the best scientific and commercial information available
we consider the effects from disease and predation to be a threat to
Arctostaphylos franciscana. Infection of the plant by Phytophthora
cinnamomi or other Phytophthora species has been determined to be a
serious threat to A. franciscana because only one plant occurs in the
wild, the disease is easily and quickly spread by multiple vectors, and
at least six species of Phytophthora are known to be present in the
vicinity of the San Francisco peninsula. Additionally, we consider
predation to be a relatively minor but ongoing threat to the wild
population of the species. Although the leaf roller moth has not been
known to kill Arctostaphylos species, the moth produces five
overlapping generations per year and severely damaged the leaves in
2010. Predation on branches by California voles has occurred and is
also relatively minor but ongoing threat.
D. The Inadequacy of Existing Regulatory Mechanisms
Regulatory mechanisms protecting Arctostaphylos franciscana derive
primarily from the location of the single known wild plant on GGNRA
lands on the Presidio, which are administered by the Presidio Trust.
The Presidio Trust was established by the Presidio Trust Act of 1996 to
manage the leasing, maintenance, rehabilitation, repair, and
improvement of property within the Presidio (Presidio Trust Act, as
amended, sec. 104(a)). The Presidio Trust is directed to preserve the
natural, scenic, cultural, and recreational resources on the Presidio,
but also is directed to ensure that the Presidio becomes financially
self-sufficient by 2013 (Presidio Trust 2002, pp. 1, 2, 12). The
Presidio Trust Act directed that the Presidio Trust design a management
program to reduce NPS expenditures and increase revenues to the Federal
Government to the maximum extent possible (Presidio Trust Act, pp. 5,
6). The Presidio Trust Management Plan was published in May 2002. The
Presidio Trust manages most of the Presidio (Area B), and NPS retains
jurisdiction over Area A as defined in the Presidio Trust Management
Plan (Presidio Trust 2001, p. 3). The Presidio Trust and NPS coauthored
the Presidio Vegetation Management Plan. For special status plants, the
plan provides an objective to preserve and enhance rare plant habitats
by evaluating species-specific habitat needs, giving high priority to
actions that preserve and enhance those habitats (Presidio Trust 2001,
Chapter 3, unpaginated).
Federal regulations for the Presidio Trust, which offer some
protection to Arctostaphylos franciscana, include prohibitions on
disturbing, injuring, removing, possessing, digging, defacing, or
destroying from its natural state, any plant or parts thereof.
Unauthorized introduction of plants and plant seeds is also prohibited,
offering limited protection against invasive, nonnative species.
Additional regulations require that special events be permitted by the
Presidio Trust, and provide for restricting visitor use to address
resource conflicts (36 CFR part 1002).
The Presidio Trust is a new model for National Park management in
that the Presidio Trust is directed to preserve the natural, scenic,
cultural, and recreational resources on the Presidio and at the same
time ensure that the Presidio becomes financially self-sufficient by
2013 (Presidio Trust 2002, pp. 1, 12). This means that generation of
revenue is a consideration for the Presidio Trust's activities, as well
as resource protection. The cost of operation and care are higher for
this park than for most National Parks because of the Presidio's large
number of structures and cultivated landscapes (Presidio Trust 2011,
unpaginated). The mission of NPS on the Presidio, as stated in the
Golden Gate National Recreation Area Addition Act of 1992 (16 U.S.C.
460bb), although similar to the Presidio Trust Act regarding the
protection of natural, historic, scenic, and recreational values, does
not include the mandate to ensure that the Presidio becomes financially
self-sufficient.
The future status of the Presidio as National Park land is
uncertain, as explained in the Presidio Trust Act's section 104(o)
(Reversion), which states: ``If, at the expiration of 15 years, the
Trust has not accomplished the goals and objectives of the plan
required in section 105(b) of [the Presidio Trust Act], then all
property under the administrative jurisdiction of the Trust pursuant to
section 103(b) of [the Presidio Trust Act] shall be transferred to the
Administrator of the General Services Administration to be disposed of
in accordance with the procedures outlined in the Defense Authorization
[[Page 54445]]
Act of 1990 (104 Stat. 1809), and any real property so transferred
shall be deleted from the boundary of the Golden Gate National
Recreation Area. In the event of such transfer, the terms and
conditions of all agreements and loans regarding such lands and
facilities entered into by the Trust shall be binding on any successor
in interest.'' This clause indicates that lands currently considered
National Parks lands could be disbursed to the private sector and
subject to development within the near future. The Presidio Trust
states, however, that since 2004, the Trust's earned revenue has offset
operating costs and expects that the Presidio will meet the goal of
being a self-sustaining National Park in 2012 (Middleton 2011, p. 2).
Arctostaphylos franciscana is not listed under the California
Endangered Species Act. The conservation plan and MOA are not
regulatory in nature and not legally enforceable by third parties
(Caltrans 2009, p. 8; Chasse et al. 2009, p. 3), limiting their
usefulness in enforcing protections for the plant. Although general
protections are provided for plants on National Parks, no regulatory
language in any Park Service or Presidio Trust documents specifically
addresses protection of A. franciscana.
Based on the best scientific and commercial information available,
we consider the inadequacy of existing regulatory mechanisms not to be
a threat to the species.
E. Other Natural or Manmade Factors Affecting Its Continued Existence
Potential threats to Arctostaphylos franciscana include changes in
environmental conditions resulting from climate change, trampling or
disturbance by people visiting the Presidio, altered fire regime, loss
of genetic diversity, loss of pollinators, and stochastic (chance)
events.
Climate Change
Our analyses under the Act include consideration of ongoing and
projected changes in climate. The terms ``climate'' and ``climate
change'' are defined by the Intergovernmental Panel on Climate Change
(IPCC). ``Climate'' refers to the mean and variability of different
types of weather conditions over time, with 30 years being a typical
period for such measurements, although shorter or longer periods also
may be used (IPCC 2007, p. 78). The term ``climate change'' thus refers
to a change in the mean or variability of one or more measures of
climate (e.g., temperature or precipitation) that persists for an
extended period, typically decades or longer, whether the change is due
to natural variability, human activity, or both (IPCC 2007, p. 78).
Various types of changes in climate can have direct or indirect effects
on species. These effects may be positive, neutral, or negative and
they may change over time, depending on the species and other relevant
considerations, such as the effects of interactions of climate with
other variables (e.g., habitat fragmentation) (IPCC 2007, pp. 8-14, 18-
19). In our analyses, we use our expert judgment to weigh relevant
information, including uncertainty, in our consideration of various
aspects of climate change.
Changes in environmental conditions resulting from climate change
may cause presently suitable habitat to become unsuitable for endemic
California plants, due to projected changes in temperature and rainfall
(Loarie et al. 2008, pp. 1-2). A U.S. Geological Survey (USGS) study in
National Park lands in northern California and Oregon is underway to
examine trends in climate, ocean conditions, and other features (Madej
et al. 2010, p. 7). In these National Park lands, variation in abiotic
factors (for example, precipitation, fog, and air and ocean
temperatures) regulates many ecological processes, including the
distribution of vegetation and frequency of disturbance from fires,
floods, landslides, and pest species. The preliminary results of the
USGS study show an increase in average maximum summer air temperatures
at GGNRA, near the Presidio (Madej et al. 2010, p. 24).
Summer fog and overcast along the California coast has been
identified as ecologically important to endemic plant species by
increasing water availability during the dry summer months, reducing
loss of water from leaves (evapotranspiration), and decreasing the
frequency of drought stress (Fischer et al. 2009, pp. 792-794). Fog
frequency along the Pacific coast is highest in north and central
California and declines in Oregon and southern California (Johnstone
and Dawson 2010, p. 4534). Climate change may be affecting the amount
and duration of fog and cloud cover along the California coast
including within the San Francisco Bay area. Mean fog frequency in the
California region, quantified by cloud ceiling height measured at
airports, has decreased since 1951 (Johnstone and Dawson 2010, p.
4535). Research by Vasey (2010, p. 1) suggests that most coastal
endemic Arctostaphylos species are more vulnerable to drought stress
than those found in interior California, and could be threatened by a
decrease in coastal summer fog. He found that obligate-seeding
Arctostaphylos species, such as A. franciscana, are better hydrated in
areas that receive fog. He also found that coastal obligate-seeding
species are more vulnerable to vascular cavitation (blockage forming in
water vessels in the plant) when the rate of water loss through the
leaves becomes too great, such as during drought (Vasey 2010, p. 1).
This disruption of water flow can lead to branch death and possibly
death of the entire plant (Vasey 2010, p. 1).
Reduced soil moisture from decrease in summer fog may also result
in reduced seed germination and seedling survival. Additionally, the
ability of Arctostaphylos franciscana to respond to future climate
changes by establishing new plants in new habitat may be limited
because of the plant's association with serpentine and greenstone
bedrock outcrops (Service 2003, pp. 95, 96), and because soils derived
from serpentine and greenstone bedrock on the peninsula are limited in
area and largely fragmented (Chasse 2010, p. 1). Natural movement of
the species by seed dispersal to reach cooler, moister areas to the
north would be impeded by barriers such as the San Francisco Bay.
Increased temperatures within Arctostaphylos franciscana habitat
could also result in higher soil temperatures that would favor
Phytophthora cinnamomi, which reproduces best at warmer soil
temperatures. Higher temperatures would also increase the likelihood of
water stress on A. franciscana, increasing its susceptibility to other
Phytophthora species (Swiecki 2011, p. 1).
Alteration of the Natural Fire Regime
In addition to soil type and climate, fire plays a critical role in
the determination of plant distribution (Keeley 2007, p. 19). The
chaparral plant community, of which Arctostaphylos is an important
member, is adapted to specific fire regimes that vary in different
parts of California. In the San Francisco East Bay region, the current
fire return interval is estimated at about 100 years (Keeley 2007, p.
20). Factors that affect the fire frequency in the San Francisco Bay
area include a short fire season, moist climate, the local human
population density, and changes in human behavior. Due to prevailing
ocean winds and frequent fogs, the average relative humidity along the
coast is moderate to high throughout the year. The exceptions typically
occur in the fall, when changing prevailing weather patterns allow dry
northeasterly winds from the State's interior to reduce
[[Page 54446]]
humidity in the coastal area to around 20 percent, thereby creating dry
and windy conditions that typify high fire danger (GGNRA 2005, pp. 136,
140).
Fire frequency in the San Francisco Bay area has varied
substantially in the last several thousand years. Not only have the
fire regimes changed with changing climate, fire regimes have changed
as patterns of human utilization of the landscape have changed.
Disturbances by fire occurred at long intervals in the prehuman period,
then at shorter intervals during the late Native American and Spanish-
Mexican periods, and at moderate intervals during the European
settlement period. Fire disturbance intervals since the 1900s have
generally returned to long intervals in the modern period due to active
fire suppression (GGNRA 2005, pp. 144-147). The natural fire regime has
been heavily altered by the urbanization of San Francisco and
fragmentation of remaining undeveloped lands. Nearly all land within
the City of San Francisco has been developed, with the exception of
small, isolated parcels and undeveloped hilltops. Lands administered by
NPS and the Presidio Trust are surrounded by other land uses, and are
close to the wildland-urban boundary where landscape plants and
nonnative plants contribute to vegetative buildup (GGNRA 2005, pp. 130-
131) that can increase fire danger. Additionally, fire suppression over
the last 100 years has led to an increase in crown and surface fuels,
which contribute to high-intensity fires (GGNRA 2005, p. 147). In spite
of the increased fire danger on these managed lands, they could
eventually be identified as suitable for outplanting Arctostaphylos
franciscana seedlings due to the limited amount of remaining habitat.
As stated above in the Species Information section above,
Arctostaphylos franciscana is an obligate-seeding species and
reproduces primarily from seed rather than from burls after a fire
(Vasey 2010, p. 1). Two opposing types of changes in fire frequency can
threaten chaparral species such as Arctostaphylos franciscana. First,
``senescence risk'' occurs when too little fire leads to the loss of a
species dependent on fire for regeneration. The second, ``immaturity
risk,'' is a threat primarily to obligate-seeding species such as A.
franciscana. In this case, wildfires that occur too frequently may kill
plants before they can reach reproductive maturity and produce seed
(Keeley 2007, p. 18). Wildfire can substantially reduce the number of
live seeds in the soil (Odion and Tyler 2002, p. 1). Odion and Tyler
(2002 p. 1) found that a controlled burn in a 40-year-old stand of A.
morroensis (Morro manzanita), a species also occurring in maritime
chaparral, reduced the seedbank to 33 percent of that which had
accumulated in the soil since the previous burn 40 years earlier. Three
years after the burn, the new population of A. morroensis that had
germinated from the seedbank was less than half the size of the
original population (Odion and Tyler 2002, p. 1). Odion and Tyler (2002
p. 2) concluded that if viable seed densities in the soil are low
because fires are too frequent to allow seeds to accumulate in the
soil, the population may risk extinction.
The fire return interval for this general area, and, therefore, for
Arctostaphylos franciscana, is currently approximately 100 to 125 years
(Parker pers. comm., 2011; Vasey 2011a, p. 1). The long fire return
interval is not thought to be a threat to the mature A. franciscana
plant at the Presidio or to any seedlings likely to be outplanted on
the Presidio in the future. Infrequent fire would allow the mature
plant at the Presidio to produce seed and build up a sufficiently large
seedbank to withstand seed loss from wildfire, and would allow the
growth of outplantings in other suitable areas. However, if fire
continues to be excluded from the plant's location at the Presidio and
the fire return interval greatly exceeds the natural return interval,
over time the loss of fire may also result in the loss of the mature
plant and individual outplanted seedlings due to competition by other
plants, including nonnative plants, that could encroach upon the
manzanita.
Other aspects of the altered fire regime within the remaining
undeveloped lands of San Francisco pose greater threats to the species.
Alteration of the fire regime has led to an increase in crown and
surface fuels in some areas, leading NPS fire planners to conclude that
it is difficult to predict the effects of the changed fire regime,
given the trend to warmer and drier climate conditions (Johnstone and
Dawson, 2010, p. 4535; Madej et al. 2010, p. 24) and the relationship
between climate and fire frequency (GGNRA 2005, pp. 147, 148). In the
past, large fires have occurred within areas that are typically subject
to maritime climatic conditions. Such fires include the 1923 Berkeley
Fire, the October 1991 Oakland Fire (Keeley 2005, p. 286) that burned
607 ha (1,500 ac), the October 1995 fire at Point Reyes National
Seashore that burned 4,999 ha (12,354 ac) (GGNRA 2005, p. 151), and the
1,133-ha (2,800-ac) 2009 Lockheed Fire north of the City of Santa Cruz
(The Associated Press 2009). On the Presidio, fire history data show
that 17 fires occurred between 2000 and 2009, with no fires in some
years and as many as 5 fires in other years. All fires were contained
at 0.04 ha (0.1 ac) or less (A. Forrestel, pers. comm., 2011a, 2011b).
In the same period, approximately four wildfires occurred in the Marin
Headlands, directly north of the Presidio across the Golden Gate, while
recent fire history records for all areas of the GGNRA show the
potential for larger wildfires in the maritime zone (GGNRA 2005, pp.
150-155).
Although the Presidio is located within a highly urbanized setting,
substantial areas of open space within the Presidio itself and within
the adjacent GGNRA lands contain an interspersed mixture of vegetative
types, including native vegetation, landscaped grounds, and forest
(GGNRA 2005, pp. 190-199; Presidio Trust 2011, unpaginated). Grasslands
are now dominated by nonnative annual grasses and forbs, which burn
with greater intensity and at a more rapid rate of spread than
grasslands dominated by native species (GGNRA 2005, p. 192). According
to a fire model prepared by the GGNRA, areas that they manage on the
western and southwestern borders of Presidio Trust lands present a
moderate and moderate-high fire hazard (GGNRA 2005, p. E-7). The
altered fire regime may result in infrequent fires that burn larger and
hotter than previously, with the potential for greater loss of the
seedbank. Alternatively, the incidence of wildfire could increase,
which would be detrimental to Arctostaphylos franciscana by killing
mature plants, seedlings, and seeds in the seedbank. In obligate-
seeding species, such as A. franciscana, fire normally kills the adult
plants, which are then replaced by plants that germinate from seed in
the soil seedbank. A wildfire that would kill the single wild A.
franciscana plant would be an especially serious threat to the future
of the species because no A. franciscana seedbank has been found in
soil collected from the area beneath the wild plant (Young 2011, p. 1).
Visitor Use
Impacts due to visitor use could harm the wild plant. The
translocated wild plant has been planted in an active native plant
management area that receives heavy public use, although it is
protected from public access by a post and cable fence and is monitored
(Chasse et al. 2009, pp. 20-28). The post and cable fence is placed
along an adjacent trail so that people do not enter the immediate area
around the plant;
[[Page 54447]]
however, an event in which a visitor treads on the plant could result
in damage to the wild plant. Over time, incremental damage could result
in the decline of the plant. The fence appears to be effective,
although its wire mesh has been bent either by employees and volunteers
or by the general public crossing the fence (Estelle 2012b, p. 2).
Presidio Trust staff has stated that, on a few occasions, volunteers
and members of the general public have asked permission to visit and
photograph the plant, and that volunteers who work with the plant have
been requested to not disclose its location (Estelle 2012c, p. 1). As
noted under Factor B, the Presidio Trust and NPS have made serious
efforts not to reveal the location of Arctostaphylos franciscana
because they are concerned that public knowledge of its location would
attract large numbers of plant enthusiasts who may damage the A.
franciscana and compact the soil (Thomas, pers. comm., 2011). If
trampling of the A. franciscana occurs, the Presidio Trust could take
three protective actions: a fence could be placed around the plant,
interpretive signs could be placed near the plant, and volunteers or
interns could be made available to talk to visitors (Thomas, pers.
comm., 2012).
The wild Arctostaphylos franciscana plant may be susceptible to
damage from soil compaction due to foot traffic. Roots grow into soil
to maintain stability and extract water and nutrients; however, soil
compaction increases the resistance of the soil to root penetration and
thus diminishes the plant's ability to extract sufficient water and
nutrients (Hammitt and Cole 1998, p. 52). Soil compaction also reduces
water infiltration rates and soil aeration by collapsing the larger
pores in the soil. Reduced soil oxygen levels from loss of soil pores
also can impact root growth, which would further reduce water and
nutrient uptake (Hammitt and Cole 1998, p. 52). Additionally, soil
compaction has been found to cause considerable damage to mycorrhizal
fungi in seedling roots (Waltert et al. 2002, p. 1). As noted in the
Historical Distribution and Habitat section, most Arctostaphylos
species form strong symbiotic associations with soil mycorrhizal fungi,
which develop an external sheath surrounding the plant's roots. All
water and nutrients pass through this sheath to the plant's roots
rather than directly from the soil to the plant's roots (Chasse 2009,
p. 12). Damage from soil compaction would not only impact the wild
plant by reducing its ability to take up water and nutrients, but could
also reduce the survival of seedlings near the wild plant.
Soil compaction also favors the growth of Phytophthora. Poor
drainage resulting from compaction facilitates the dispersal of
swimming zoospores that infect the host plant (Swiecki 2011, p. 2).
Additionally, anaerobic (lack of oxygen) stress associated with
saturated soil conditions increases the susceptibility of roots to
Phytophthora infections (Swiecki 2011, p. 2).
Vandalism
The location of the Arctostaphylos franciscana plant within the
Presidio is near common-use trails and an area available for private
and public events. Threats to A. franciscana include damage from
vandalism. Vandalism to trees was reported in the Presidio in the early
2000s (Thomas pers. comm. 2011). Severe vandalism was observed in
Golden Gate Park, located approximately 1.5 mi (2.4 km) south of the
Presidio, in summer 2010, when more than 40 trees and 30 rose bushes
were destroyed by unknown persons for unknown reasons (Gordon 2010,
unpaginated; King 2010, unpaginated). The post and cable fence that
protects the wild A. franciscana plant is approximately 30 ft (9.1 m)
from the plant and is not constructed to completely exclude visitors.
In the unlikely event that vandalism occurs, the results could be
serious because there is only one wild plant.
Stochastic Events and Small Population Size
Chance events constitute a serious threat to Arctostaphylos
franciscana. Because the known population of A. franciscana in the wild
is currently limited to a single plant, the species is extremely
vulnerable to stochastic events--normal but damaging environmental
perturbations and catastrophes such as droughts, storm damage, disease
outbreaks, and fires, from which large, wide-ranging populations can
generally recover, but which may lead to extirpation of small, isolated
populations (Gilpin and Soule 1986, pp. 25-31). The majority of the
remaining habitat associated with A. franciscana occurs within rock
outcrops on hilltops or slopes surrounded by development or along
coastal cliffs. These areas, because of their limited size and
proximity to developed areas, are more likely to experience inadvertent
fire or environmental degradation (altered hydrologic regime; increased
introduction of nonnative, invasive plants; and increased spread of
disease). The nature of the habitat associated with A. franciscana
(rock outcrops, thin soils, sloped or hilltop terrain) may also
increase the effects of drought. By nature these habitats generally do
not have the water-holding capacity of deeper soiled, level habitats.
Because some of the remaining habitat associated with the species is
along coastal bluffs or on hillsides, these areas may also be more
susceptible to landslides or erosion during excessively wet
precipitation events. As a result, we consider stochastic events to be
of significant threat for this species.
Any new population that starts from the single wild plant is likely
to have reduced genetic variation compared to historical populations.
Even if the number of plants increases, it may not reverse the previous
genetic loss, known as the bottleneck effect (Allendorf and Luikart
2007, p. 158). Bottlenecks generally have a greater and more lasting
effect on the loss of genetic variation in species with slow growth
rates (long-lived species with few offspring) (Allendorf and Luikart
2007, p. 133). The age of the single wild Arctostaphylos franciscana
plant is estimated at 60 years, and no other A. franciscana plants or
seedlings were found associated with the wild plant. Reduced genetic
variation may result in the inability of future generations of the
plant to adapt to changes in habitat, such as decrease in fog and
increase in temperature (see Climate Change discussion above) or loss
of pollinators (see discussion below). While Arctostaphylos franciscana
may be capable of self-pollination, in general, self-pollination
results in decreased genetic variation in the offspring of a plant
(Allendorf and Luikart 2007, p. 123). Therefore, loss of genetic
variation is expected if A. franciscana is dependent on self-
pollination to produce seed. Based on the above discussion, we have
determined that the loss of genetic variation is a significant threat
for this species.
The wild plant is also threatened by the Allee effect, a decline in
population growth rate due to declining plant density (Ak[ccedil]akaya
et al. 1999, p. 86). For the wild Arctostaphylos franciscana plant, the
Allee effect may result from a lack of other available A. franciscana
plants with which to cross-pollinate and produce viable seed. The wild
plant, the single remaining individual of its species in the wild, is
currently dependent on its ability to self-pollinate, which may be
limited, and the efforts of researchers and Presidio staff to provide
additional plants of different genotypes (if they are proven to be A.
franciscana) from botanical garden specimens to cross-pollinate
[[Page 54448]]
with the wild plant to produce new individuals and populations.
Loss of Pollinators
Suitable pollinators may be critical for seed production for this
obligate-seeding species. If pollinators are absent, or present in
insufficient numbers, there may be a lack of viable seeds to develop
and maintain the seedbank. In a study of the effects of habitat
fragmentation on a non-self-pollinating plant (Lennartsson 2002, pp.
3065, 3066, 3068), the author found that fragmented populations
exhibited dramatically reduced seed set and population viability, both
of which were caused by a reduction in the number of pollinators.
Pollinators have been observed on the wild A. franciscana plant;
however, no surveys have been completed to identify the most important
pollinators. The most frequent pollinators seen have been bees and
bumblebees. Hummingbirds and butterflies have also been observed
visiting the flowers, likely because few other plants are blooming
during the winter months when A. franciscana blooms (Vasey, pers. comm.
2010). Although the loss of seed produced in a single year would not
likely lead to the extirpation of the species, the continued reduction
of the seed crop or dependence on self-pollination would reduce the
seedbank, genetic variation, and the potential for population
expansion.
Hybridization
Cultivars of Arctostaphylos franciscana are used in the commercial
nursery trade. The cultivars (varieties of a plant produced and
maintained by cultivation) are likely descended from some of the last
wild A. franciscana plants known to exist in the 1940s, and are located
in at least four botanical gardens (Chasse et al. 2009, pp. 7, 8).
Because hybridization between diploid species of Arctostaphylos is well
recognized (Chasse et al. 2009, p. 5), there is a good chance that many
of these commercially available specimens have resulted from hybrid
seed. Because of the threat of cross-pollination from hybrids or other
species (Allendorf et al. 2001, pp. 613, 618-621), any propagation or
reintroduction programs for A. franciscana must account for subsequent
contamination of the A. franciscana gene pool. The conservation plan
takes this into account by recommending that future outplantings of
nursery-raised cuttings or seedlings of the recently discovered A.
franciscana plant avoid areas that could facilitate cross-pollination
(Chasse et al. 2009, p. 31). Appropriate outplanting areas will be
determined by A. franciscana experts, in cooperation with NPS, the
Presidio Trust, and the Golden Gate National Parks Conservancy (Chasse
et al. 2009, p. 31). Although cross-pollination of the wild plant with
hybrids and the production of hybrid seed is possible, we do not know
if this is a substantial threat to the species.
Based on the best scientific and commercial information available,
we consider that Arctostaphylos franciscana is negatively impacted by
other natural or manmade factors affecting its continued existence
which include changes in environmental conditions resulting from
climate change, altered fire regime, soil compaction from visitor use,
vandalism, loss of genetic diversity, loss of pollinators, stochastic
events, effects of small population size, and hybridization.
Cumulatively, we consider these threats to be significant and ongoing.
Cumulative Impacts
Some of the threats discussed in this finding could work with one
another to cumulatively create situations that potentially impact
Arctostaphylos franciscana beyond the scope of the individual threats
we have already analyzed. In particular, climate change may exacerbate
many of the threats discussed in this final rule. For example, warmer,
drier conditions in the range of the species could result in not only
less summer fog and increased water stress leading to plant death, but
could also create more suitable conditions for infection by
Phytophthora species and result in more fires. The loss of native
habitat due to urban development within the range of A. franciscana has
likely reduced pollinator nesting areas and numbers of native plants
that provide nectar and pollen. Climate change could increase the loss
of pollinators if the abundance of flowers preferred by pollinators
decreases and the synchrony of bloom periods and pollinator emergence
is disrupted. Although there currently are no data available regarding
changes in plant bloom periods or emergence dates of pollinators in the
Presidio in response to climate change, Forister and Shapiro (2003, p.
1130) found that over a period of 31 years warmer and drier winter
conditions were associated with earlier butterfly appearance in the
Central Valley of California. The ability of A. franciscana to self-
pollinate may be limited (Parker 2011, p. 1); therefore, we expect that
bumblebees, bees, and other insects are likely needed for A.
franciscana to produce seed. Nitrogen enrichment of the soil from
atmospheric deposition may encourage the growth of nonnative, invasive
grasses in the vicinity of the wild plant. The grasses could, in turn,
provide additional habitat for rodents such as California voles that
feed on the wild plant.
Determination
We have carefully assessed the best scientific and commercial
information available regarding past, present, and future threats to
Arctostaphylos franciscana. The primary threat to A. franciscana is
from the present or threatened destruction, modification, or
curtailment of the species' habitat or range (Factor A). All original
occupied habitat of the species has been lost, and its current range
has been reduced to a single location that supports a single A.
franciscana plant. The last wild plant was moved from its native
habitat, which was subsequently destroyed during a highway construction
project, and transplanted to natural habitat on the Presidio in San
Francisco. Limited remaining suitable habitat is available to support a
viable population of the species. Although greenstone and serpentine
soils remain on the peninsula, the majority of this land has been
fragmented and may be subject to edge effects and nitrogen deposition.
Additionally, the possible transfer of Presidio lands to the GSA and
the private sector may result in potential future loss of the plant or
modification of its habitat.
Overutilization (Factor B) is a threat because the current known
wild population consists of one individual plant, and Arctostaphylos
plants are popular for landscaping and other horticultural purposes.
Arctostaphylos franciscana is thus vulnerable to overcollection or
damage if visitors harvest cuttings or seeds.
Disease and predation (Factor C).is also a threat to Arctostaphylos
franciscana. Stress from transplanting the wild plant may have weakened
the plant and made it more susceptible to disease and predation. The
plant was heavily infested with a native leaf roller moth after being
transplanted; however, the caterpillars and damaged foliage were
removed and the plant has produced new foliage and flowers. Minor
damage to Arctostaphylos franciscana branches from gnawing by
California voles and other rodents has also been observed. Twig blight,
a fungal infection, was observed on the plant during the winter of
2009-2010, but the infection subsided during the dry season. Infection
by Phytophthora species, especially Phytophthora cinnamomi, is a
serious and lethal problem among Arctostaphylos species
[[Page 54449]]
in the wild and in the native plant nursery trade. Phytophthora
cinnamomi cannot be controlled once introduced to a plant or habitat,
and results in plant death. Many A. franciscana cuttings are being
grown in commercial or university nurseries for outplanting with the
wild plant. Although the use of clean propagation techniques has been
requested by the staff in charge of the project, the risk of infection
of the cuttings and wild plant by P. cinnamomi is still a threat. At
least six other species of Phytophthora are also found south of the San
Francisco peninsula and could be introduced into the vicinity of the
wild plant. In addition, the pathogen that causes sudden oak death has
been discovered in the Presidio; however, the threat of this disease to
A. franciscana is likely not severe.
Existing regulatory mechanisms (Factor D) afford certain
protections for Arctostaphylos franciscana because the plant is located
on lands administered by NPS, GGNRA, and the Presidio Trust. However,
as mentioned above, these protections are not specific to A.
franciscana. Because no existing regulatory mechanisms exist specific
to A. franciscana, we do not consider the existing regulatory
mechanisms to be inadequate to protect the species.
Other natural or manmade factors affecting Arctostaphylos
franciscana's continued existence (Factor E) include environmental
effects resulting from climate change, alteration of the natural fire
regime, soil compaction from visitor use, vandalism, loss of genetic
diversity, stochastic events, small population size, loss of
pollinators, and hybridization are also threats to this species.
Changes in the climate are expected to include increased air
temperature and reduced summer fog, both resulting in warmer and drier
conditions to which the plant may be less well-adapted. Additionally,
climate change may result in divergence between the timing of flowering
of A. franciscana and the availability of suitable pollinators,
negatively affecting the plant's ability to set seed. Climate change
may also reduce pollinator species and numbers. Warming and drying of
the plant's habitat would likely also increase the frequency of
wildfire, which could result in death of the wild plant and its future
seedlings if fire occurred before the plants were able to produce
viable seeds. Loss of mature Arctostaphylos plants to fire is a natural
phenomenon; however, this species is currently represented by a single
mature plant. Therefore, to our knowledge, the loss of the plant would
result in extinction of the species in the wild. Loss of genetic
diversity has likely already occurred due to the reduction of the
species to a single wild plant and is expected to continue because this
generally outcrossing species will be limited to self-pollination.
Reduced genetic diversity may also limit the species' ability to adapt
to changes in habitat, such as those resulting from climate change or
loss of pollinators. The species is extremely vulnerable to stochastic
events such as droughts, storm damage, and fires, from which large
wide-ranging populations can generally recover, but which would likely
drive a species consisting of a single plant to extinction.
Based on our evaluation of the best available scientific and
commercial information regarding the past, present, and future threats
faced by Arctostaphylos franciscana, we have determined that the
continued existence of A. franciscana is threatened by overutilization
for commercial and recreational purposes, disease, and predation,
climate change, alteration of the natural fire regime, soil compaction
from visitor use, vandalism, loss of genetic diversity, stochastic
events, small population size, loss of pollinators, and hybridization.
Because the species faces these threats throughout its extremely
limited range, we find that A. franciscana is in danger of extinction
throughout its entire range and, therefore, it is unnecessary to
analyze its status in any significant portion of its range.
The Act defines an endangered species as one that is in danger of
extinction throughout all or a significant portion of its range. A
threatened species is one that is likely to become an endangered
species in the foreseeable future throughout all or a significant
portion of its range. The species in the wild currently exists as a
single plant on the San Francisco Presidio. Because the range of the
species is restricted to a single plant, the risks presented by the
threats discussed herein are more intensified than they would be were
the species more widespread or numerous. Based on our evaluation of the
best available scientific and commercial information, and given the
current population size (one wild plant) and severely limited
distribution throughout its historical range, we have determined the
species is currently on the brink of extinction in the wild and
therefore is in danger of extinction throughout all of its range. As a
result, this species meets the definition of an endangered species
under the Act. Because the species is in danger of extinction now due
to its limited population size and the severity of existing threats, as
opposed to in the foreseeable future, A. franciscana meets the
definition of an endangered species rather than a threatened species.
On the basis of our careful evaluation of the best available scientific
and commercial information regarding the past, present, and future
threats to the species as discussed above relative to the listing
factors, we are listing Arctostaphylos franciscana as an endangered
species throughout its range.
Available Conservation Measures
Conservation measures provided to species listed as endangered or
threatened under the Act include recognition, recovery actions,
requirements for Federal protection, and prohibitions against certain
practices. Recognition through listing results in public awareness and
conservation by Federal, State, and local agencies; private
organizations; and individuals. The Act encourages cooperation with the
States and requires that recovery actions be carried out for all listed
species. The protection measures required of Federal agencies and the
prohibitions against certain activities are discussed, in part, below.
Section 7(a) of the Act requires Federal agencies to evaluate their
actions with respect to any species that is proposed or listed as
endangered or threatened and with respect to its critical habitat, if
any is designated. Regulations implementing this interagency
cooperation provision of the Act are codified at 50 CFR part 402.
Section 7(a)(4) of the Act requires Federal agencies to confer with the
Service on any action that is likely to jeopardize the continued
existence of a species proposed for listing or result in destruction or
adverse modification of proposed critical habitat. If a species is
listed subsequently, section 7(a)(2) of the Act requires Federal
agencies to ensure that activities they authorize, fund, or carry out
are not likely to jeopardize the continued existence of the species or
destroy or adversely modify its critical habitat. If a Federal action
may affect a listed species or its critical habitat, the responsible
Federal agency must enter into formal consultation with the Service.
Federal agency actions within the species' habitat that may require
conference or consultation or both, as described in the preceding
paragraph, include land management, road construction, and any other
landscape altering activities, such as invasive tree and plant removal,
within the known range of the species or within any designated critical
habitat.
The Act and its implementing regulations set forth a series of
general prohibitions and exceptions that apply
[[Page 54450]]
to endangered plants. All prohibitions of section 9(a)(2) of the Act,
implemented by 50 CFR 17.61, apply. When this final rule becomes
effective (see DATES section above), Arctostaphylos franciscana, the
last wild specimen (including any plants propagated from the wild
plant) and the botanical garden specimens (those plants previously
collected from the wild and subsequently propagated), will be protected
by all prohibitions of section 9(a)(2) of the Act, which protects
listed plants in areas of Federal jurisdiction such as the Presidio.
Plants that have been or are being sold in the nursery trade or have
been transplanted into home gardens will not be considered part of the
listed entity.
These prohibitions, in part, make it illegal for any person subject
to the jurisdiction of the United States to import or export, transport
in interstate or foreign commerce in the course of a commercial
activity, sell or offer for sale in interstate or foreign commerce, or
remove and reduce the species to possession from areas under Federal
jurisdiction. In addition, for plants listed as endangered, the Act
prohibits the malicious damage or destruction on areas under Federal
jurisdiction and the removal, cutting, digging up, or damaging or
destroying of such plants in knowing violation of any State law or
regulation, including State criminal trespass law. Certain exceptions
to the prohibitions apply to agents of the Service and State
conservation agencies.
Arctostaphylos franciscana has not been listed by the State of
California. Listing also requires Federal agencies to avoid actions
that might jeopardize the species (16 U.S.C. 1536(a)(2)), and provides
opportunities for funding of conservation measures and land acquisition
that would not otherwise be available to them (16 U.S.C. 1534,
1535(d)).
We may issue permits to carry out otherwise prohibited activities
involving endangered and threatened wildlife species under certain
circumstances. Regulations governing permits are codified at 50 CFR
17.62 for endangered plants, and at 17.72 for threatened plants. With
regard to endangered plants, a permit must be issued for the following
purposes: for scientific purposes or for enhancing the propagation or
survival of the species, and for take to to prevent undue economic
hardship (see 50 CFR 17.63).
Required Determinations
Paperwork Reduction Act of 1995 (44 U.S.C. 3501 et seq.)
This rule does not contain any new collections of information that
require approval by Office of Management and Budget (OMB) under the
Paperwork Reduction Act. This rule will not impose recordkeeping or
reporting requirements on State or local governments, individuals,
businesses, or organizations. An agency may not conduct or sponsor, and
a person is not required to respond to, a collection of information
unless it displays a currently valid OMB control number.
National Environmental Policy Act
We have determined that environmental assessments and environmental
impact statements, as defined under the authority of the National
Environmental Policy Act of 1969 (42 U.S.C. 4321 et seq.), need not be
prepared in connection with regulations pursuant to section 4(a) of the
Act. We published a notice outlining our reasons for this determination
in the Federal Register on October 25, 1983 (48 FR 49244).
References Cited
A complete list of all references cited in this rule is available
on the Internet at https://www.regulations.gov or upon request from the
Field Supervisor, Sacramento Fish and Wildlife Office (see ADDRESSES).
Authors
The primary authors of this document are the staff members of the
Sacramento Fish and Wildlife Office (see ADDRESSES).
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 follows:
PART 17--[AMENDED]
0
1. The authority citation for part 17 continues to read as follows:
Authority: 16 U.S.C. 1361-1407; 16 U.S.C. 1531-1544; 16 U.S.C.
4201-4245; Pub. L. 99-625, 100 Stat. 3500; unless otherwise noted.
0
2. Amend Sec. 17.12(h) by adding an entry for ``Arctostaphylos
franciscana'' (Franciscan manzanita) to the List of Endangered and
Threatened Plants in alphabetical order under FLOWERING PLANTS, to read
as follows:
Sec. 17.12 Endangered and threatened plants.
* * * * *
(h) * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species
---------------------------------------------------------- Historic range Family Status When Critical Special
Scientific name Common name listed habitat rules
--------------------------------------------------------------------------------------------------------------------------------------------------------
Flowering Plants
* * * * * * *
Arctostaphylos franciscana........ Franciscan manzanita. U.S.A., (CA)......... Ericaceae............ E 809 NA NA
* * * * * * *
* * * * * * *
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dated: August 24, 2012.
Rowan W. Gould,
Acting Director, U.S. Fish and Wildlife Service.
[FR Doc. 2012-21742 Filed 9-4-12; 8:45 am]
BILLING CODE 4310-55-P