Endangered and Threatened Wildlife; 90-Day Finding on a Petition To List the Bull Kelp as Threatened or Endangered Under the Endangered Species Act, 40782-40789 [2023-13277]
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Council address: Mid-Atlantic Fishery
Management Council, 800 N State
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Diane M. DeJames-Daly,
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Fisheries, National Marine Fisheries Service.
[FR Doc. 2023–13278 Filed 6–21–23; 8:45 am]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
[Docket No. 230613–0148; RTID 0648–
XR128]
Endangered and Threatened Wildlife;
90-Day Finding on a Petition To List
the Bull Kelp as Threatened or
Endangered Under the Endangered
Species Act
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; 90-day petition finding.
AGENCY:
We, NMFS, announce a 90day finding on a petition to list the bull
kelp (Nereocystis luetkeana) as
threatened or endangered under the
Endangered Species Act (ESA) and to
designate critical habitat concurrent
with the listing. We have reviewed the
information presented in the petition as
well as information readily available in
our files and find that the petition does
not present substantial scientific or
commercial information indicating that
the petitioned actions may be
warranted. Therefore, we are denying
this petition.
ADDRESSES: Interested persons may
obtain a copy of the petition online at
the NMFS website: https://
www.fisheries.noaa.gov/national/
endangered-species-conservation/
negative-90-day-findings.
FOR FURTHER INFORMATION CONTACT:
Melissa Neuman, NMFS West Coast
Region, Protected Resources Division,
(562) 481–4594, Melissa.Neuman@
noaa.gov.
SUMMARY:
SUPPLEMENTARY INFORMATION:
Background
On September 1, 2022, we received a
petition from the Center for Biological
Diversity to list the bull kelp
(Nereocystis luetkeana) as a threatened
or endangered species under the ESA
and to designate critical habitat
concurrent with the listing. The petition
asserts that the bull kelp is threatened
by all of the ESA section 4(a)(1) factors:
(1) the present or threatened
destruction, modification, or
curtailment of its habitat or range; (2)
overutilization for commercial,
recreational, scientific or educational
purposes; (3) disease or predation; (4)
the inadequacy of existing regulatory
mechanisms; and (5) other natural or
manmade factors affecting its continued
existence. The petition is available
online (see ADDRESSES).
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ESA Statutory, Regulatory, and Policy
Provisions and Evaluation Framework
Section 4(b)(3)(A) of the ESA of 1973,
as amended (16 U.S.C. 1531 et seq.),
requires, to the maximum extent
practicable, that within 90 days of
receipt of a petition to list a species as
threatened or endangered, the Secretary
of Commerce shall make a finding on
whether that petition presents
substantial scientific or commercial
information indicating that the
petitioned action may be warranted, and
promptly publish such finding in the
Federal Register (16 U.S.C.
1533(b)(3)(A)). If NMFS finds that
substantial scientific or commercial
information in a petition indicates the
petitioned action may be warranted (a
‘‘positive 90-day finding’’), we are
required to promptly commence a
review of the status of the species
concerned, during which we will
conduct a comprehensive review of the
best available scientific and commercial
data. We conclude the review with a
finding as to whether, in fact, the
petitioned action is warranted within 12
months of receipt of the petition.
Because the finding at the 12-month
stage is based on a more thorough
review of the best available information,
as compared to the narrow scope of
review at the 90-day stage, a ‘‘positive
90-day’’ finding does not prejudge the
outcome of the status review.
Under the ESA, a listing
determination may address a species,
which is defined to also include
subspecies and, for any vertebrate
species, any distinct population
segment (DPS) that interbreeds when
mature (16 U.S.C. 1532(16)). A species,
subspecies, or DPS is ‘‘endangered’’ if it
is in danger of extinction throughout all
or a significant portion of its range, and
‘‘threatened’’ if it is likely to become
endangered within the foreseeable
future throughout all or a significant
portion of its range (16 U.S.C. 1532(6)
and (20)). Pursuant to the ESA and our
implementing regulations, we determine
whether species are threatened or
endangered based on any one or a
combination of the following five ESA
section 4(a)(1) factors: (1) the present or
threatened destruction, modification, or
curtailment of its habitat or range; (2)
overutilization for commercial,
recreational, scientific, or educational
purposes; (3) disease or predation; (4)
the inadequacy of existing regulatory
mechanisms; and (5) other natural or
manmade factors affecting its continued
existence (16 U.S.C. 1533(a)(1); 50 CFR
424.11(c)).
ESA-implementing regulations issued
jointly by NMFS and the U.S. Fish and
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Wildlife Service (50 CFR 424.14(h)(1)(i))
define ‘‘substantial scientific or
commercial information’’ in the context
of reviewing a petition to list, delist, or
reclassify a species as credible scientific
or commercial information in support of
the petitioner’s claims such that a
reasonable person conducting an
impartial scientific review would
conclude that the action proposed in the
petition may be warranted. Conclusions
drawn in the petition without the
support of credible scientific or
commercial information will not be
considered substantial information. In
reaching the 90-day finding on the
petition, we considered the information
described in sections 50 CFR 424.14(c)
and (d).
Our determination as to whether the
petition provides substantial scientific
or commercial information indicating
that the petitioned action may be
warranted depends in part on the degree
to which the petition includes the
following types of information: (1)
information on current population
status and trends and estimates of
current population sizes and
distributions, both in captivity and the
wild, if available; (2) identification of
the factors under section 4(a)(1) of the
ESA that may affect the species and
where these factors are acting upon the
species; (3) whether, and to what extent,
any or all of the factors alone or in
combination identified in section 4(a)(1)
of the ESA may cause the species to be
an endangered species or threatened
species (i.e., the species is currently in
danger of extinction or is likely to
become so within the foreseeable
future), and, if so, how high in
magnitude and how imminent the
threats to the species and its habitat are;
(4) information on adequacy of
regulatory protections and effectiveness
of conservation activities by States, as
well as other parties, that have been
initiated or that are ongoing, that may
protect the species or its habitat; and (5)
a complete, balanced representation of
the relevant facts, including information
that may contradict claims in the
petition. See 50 CFR 424.14(d).
If the petitioner provides
supplemental information before the
initial finding is made and states that it
is part of the petition, the new
information, along with the previously
submitted information, is treated as a
new petition that supersedes the
original petition, and the statutory
timeframes will begin when such
supplemental information is received.
See 50 CFR 424.14(g).
We may also consider information
readily available at the time the
determination is made (50 CFR
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424.14(h)(1)(ii)). We are not required to
consider any supporting materials cited
by the petitioner if the petitioner does
not provide electronic or hard copies, to
the extent permitted by U.S. copyright
law, or appropriate excerpts or
quotations from those materials (e.g.,
publications, maps, reports, letters from
authorities). See 50 CFR 424.14(c)(6);
424.14(h)(1)(ii).
The substantial scientific or
commercial information standard must
be applied in light of any prior reviews
or findings we have made on the listing
status of the species that is the subject
of the petition (50 CFR 424.14(h)(1)(iii)).
Where we have already conducted a
finding on, or review of, the listing
status of that species (whether in
response to a petition or on our own
initiative), we will evaluate any petition
received thereafter seeking to list, delist,
or reclassify that species to determine
whether a reasonable person conducting
an impartial scientific review would
conclude that the action proposed in the
petition may be warranted despite the
previous review or finding. Where the
prior review resulted in a final agency
action—such as a final listing
determination, a 90-day not-substantial
finding, or a 12-month not-warranted
finding—a petition will generally not be
considered to present substantial
scientific and commercial information
indicating that the petitioned action
may be warranted unless the petition
provides new information or analysis
not previously considered. 50 CFR
424.14(h)(1)(iii).
At the 90-day finding stage, we do not
conduct additional research and we do
not solicit information from parties
outside the agency to help us in
evaluating the petition. We accept the
petitioner’s sources and
characterizations of the information
presented if they appear to be based on
accepted scientific principles, unless we
have specific information in our files
that indicates the petition’s information
is incorrect, unreliable, obsolete, or
otherwise irrelevant to the requested
action. Information that is susceptible to
more than one interpretation, or that is
contradicted by other available
information, will not be dismissed at the
90-day finding stage, so long as it is
reliable and a reasonable person
conducting an impartial scientific
review would conclude it supports the
petitioner’s assertions. In other words,
conclusive information indicating the
species may meet the ESA’s
requirements for listing is not required
to make a positive 90-day finding. We
will not conclude that a lack of specific
information alone necessitates a
negative 90-day finding if a reasonable
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person conducting an impartial
scientific review would conclude that
the unknown information itself suggests
the species may be at risk of extinction
presently or within the foreseeable
future.
To make a 90-day finding on a
petition to list a species, we evaluate
whether the petition presents
substantial scientific or commercial
information indicating the subject
species may be either a threatened or
endangered species, as defined by the
ESA. First, we evaluate whether the
information presented in the petition, in
light of the information readily available
in our files, indicates that the petitioned
entity constitutes a ‘‘species’’ eligible for
listing under the ESA. Next, we evaluate
whether the information indicates that
the species faces an extinction risk such
that listing may be warranted; this may
be indicated in information expressly
discussing the species’ status and
trends, or in information describing
impacts and threats to the species. We
evaluate whether the petition presents
any information on specific
demographic factors pertinent to
evaluating extinction risk for the species
(e.g., population abundance and trends,
productivity, spatial structure, age
structure, sex ratio, diversity, current
and historical range, habitat integrity or
fragmentation), and the potential
contribution of identified demographic
risks to extinction risk for the species.
We then evaluate whether the petition
presents information suggesting
potential links between these
demographic risks and the causative
impacts and threats identified in section
4(a)(1) of the ESA.
Information presented on impacts or
threats should be specific to the species
and should reasonably suggest that one
or more of these factors may be
operative threats that act, or have acted,
on the species to the point that it may
warrant protection under the ESA.
Broad statements about generalized
threats to the species, or identification
of factors that could negatively impact
a species, do not constitute substantial
information indicating that listing may
be warranted. We look for information
indicating that not only is the particular
species exposed to a factor, but that the
species may be responding in a negative
fashion. We then assess the potential
significance of that negative response.
Many petitions identify risk
classifications made by
nongovernmental organizations, such as
the International Union for
Conservation of Nature (IUCN), the
American Fisheries Society, or
NatureServe, as evidence of extinction
risk for a species. Risk classifications by
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other organizations or made under other
Federal or State statutes may be
informative, but such classification
alone may not provide the rationale for
a positive 90-day finding under the
ESA. For example, as explained by
NatureServe, their assessments of a
species’ conservation status do ‘‘not
constitute a recommendation by
NatureServe for listing under the U.S.
Endangered Species Act’’ because
NatureServe assessments ‘‘have
different criteria, evidence
requirements, purposes and taxonomic
coverage than government lists of
endangered and threatened species, and
therefore these two types of lists should
not be expected to coincide’’ (https://
explorer.natureserve.org/
AboutTheData/DataTypes/Conservation
StatusCategories). Additionally, species
classifications under IUCN and the ESA
are not equivalent; data standards,
criteria used to evaluate species, and
treatment of uncertainty are also not
necessarily the same. Thus, when a
petition cites such classifications, we
will evaluate the source of information
that the classification is based upon in
light of the standards on extinction risk
and impacts or threats discussed above.
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Taxonomy
Bull kelp, Nereocystis luetkeana, is a
large brown alga in the kingdom
Chromista (single-celled and
multicellular eukaryotes with
photosynthetic plastid organelles),
phylum Gyrista, class Phaeophyceae
(brown algae), and order Laminariales
(the true kelps). Laminariales contains
three families: Alariaceae,
Laminariaceae, and Lessoniaceae.
Traditional taxonomy, largely based on
sporophyte morphology, was used to
differentiate the brown algae and
resulted in the placement of bull kelp
into the family Lessoniaceae (Springer
et al. 2007). In recent years, molecular
techniques and resulting genetic data
have challenged traditional taxonomy
within the order resulting in a
taxonomic revision at the family level
based on evolutionary relationships
(Lane et al. 2006). Bull kelp is now in
the family Laminariaceae, not
Lessoniaceae as the petitioner stated,
and it is the only species within its
genus, Nereocystis.
Distribution, Habitat, and Life History
Bull kelp is an annual marine
macroalgal species that attaches to rocky
substrates using its holdfast in intertidal
and subtidal coastal habitats in the
Northeastern Pacific Ocean from the
Aleutian Islands, Alaska, to Santa
Barbara County, California (Springer et
al. 2010). Bull kelp typically occupies
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turbulent habitats between 3–20 m
depth, and it can co-occur with other
large brown kelps including dragon kelp
(Eularia fistulosa) and giant kelp
(Macrocystis pyrifera). It is considered
to be a foundational species because it
provides habitat for a variety of other
marine organisms.
Bull kelp reproduces sexually. Adults,
also known as sporophytes, become
mature during the summer or fall
seasons at which time patches of spores,
called sori, form on the kelp blades. Sori
are shed around dawn and are
negatively buoyant, causing them to
sink. The sori release individual spores
into the water column as they sink and
upon reaching the substrate for up to
approximately four hours. During this
stage, both sori and spores have the
capacity for dispersal, but the temporal
and spatial scale of dispersal has not
been quantified to date (Springer et al.
2010). Spores have limited ability to
photosynthesize and therefore are likely
not adapted for a long planktonic life.
Given the suspected limited dispersal
distances, spores are thought to settle
near adults. Individual sporophytes
have the ability to produce and release
sori in pulses that occur every 4–6 days
with a periodicity that varies by
geographic location.
Spores that successfully settle
germinate into microscopic, sessile,
male or female gametophytes. It is
uncertain how long the gametophyte
stage persists and the length of the stage
is likely affected by abiotic conditions
such as light, nutrients, and storm
events (Springer et al. 2007). Based on
laboratory studies, gamete production
by gametophytes occurs at water
temperatures between 5–15 °C, but
when temperatures are sustained at
greater than 20 °C, morphological
abnormalities in gametophytes and
gametes are observed (Vadas 1972).
Prevailing knowledge suggests that male
gametophytes fertilize the female
gametophytes in the winter. Increased
proximity of male and female
gametophytes increases fertilization
success as does a pheromone released
by female gametophytes known as
lamoxirene. Fertilized eggs begin to
grow into sporophytes in the spring as
sunlight hours increase (Maier and
Muller 1986). As the spring growing
season progresses, macroscopic
sporophytes can grow between 6–15 cm
per day until the blades reach the water
surface during the summer months
(Springer et al. 2010 referencing Scagel
1946, Lindeberg and Lindstrom 2010).
At this point, growth slows and the
sporophyte diverts its energy to
producing spores. Typically, the life of
an individual sporophyte ends at this
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point, but Springer (2010) referring to
(Chenelot et al. 2001) points out that
individuals produced late in the season
in shallow water or wave-protected
areas may successfully overwinter and
survive a second year.
Status and Population Trends
Alaska
The petitioner cites Krumhansl et al.
(2016) when stating that population
trends of kelp are negative in the
Aleutian Islands and that bull kelp is
the primary kelp species in this region.
We did not find evidence that
Krumhansl et al. (2016) identified bull
kelp as the primary kelp species in the
ecoregion that they refer to as the
Aleutian Islands. The authors examined
an overall trend for eight species,
including bull kelp, but did not identify
species-specific trends. Information
provided by the petitioner (PNW
Herbaria Map, Springer et al. 2010) and
readily available in our files suggests
that bull kelp occurs in an area that
constitutes less than a third of the
Aleutian Island chain and bull kelp
does not occur west of the Samalga Pass,
a natural, historic biogeographic barrier
to bull kelp colonization (Konar et al.
2017). Throughout the remaining two
thirds of the Aleutian Island chain,
dragon kelp, Eualaria fistulosa, is the
dominant kelp canopy species and it
was part of the species complex
examined is the Aleutian Islands
ecoregion by Krumhansl et al. (2016).
Therefore, the petitioners are incorrect
in suggesting that the long-term trend
observed for the Aleutian Island
ecoregion is due to bull kelp declines.
Krumhansl et al. (2016) inferred
relatively high magnitude increases in
kelp abundance for the Gulf of Alaska
and the North American Pacific
Fjordland. Bull kelp is the dominant
kelp canopy species in these regions,
occurring throughout both regions with
no major breaks in distribution (https://
www.shorezone.org/). In this case, it is
reasonable to assume that bull kelp
contributed significantly to increasing
long-term trends observed by
Krumhansl et al. (2016).
In summary, the overall status of bull
kelp in Alaska indicates that
populations have increased along the
portion of the coastline where bull kelp
occurrence is consistent and known
(Gulf of Alaska and the North American
Pacific Fjordland; Krumhansl et al.
2016). In the Aleutian Islands, where
bull kelp is not a primary kelp species
and has only been observed in an area
that comprises <33% of the ecoregion,
long-term trends remain uncertain.
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Canada
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The literature cited in the petition and
the information we have readily
available in our files present limited
evidence of bull kelp decline in
Canadian waters based on long-term
trend studies conducted off the West
Coast of North America. Krumhansl et
al. (2016) inferred relatively high
magnitude increases in kelp abundance
for the North American Pacific
Fjordland from 1983–2012, and it is
reasonable to assume that bull kelp
contributed to this increasing trend
because it occurs throughout the
ecoregion with no breaks in its
distribution. Schroeder et al. (2019)
found limited evidence of bull kelp
decline in British Columbia from 2004–
2017, a time period that pre-dates and
follows the marine heat wave of 2014–
2016. In a shorter-term study along the
central coast of British Columbia, Burt
et al. (2018) found fluctuating kelp
canopy cover that may have been
related to predator/prey interactions and
found no evidence for kelp decline over
the time period they examined (2006,
2012, 2014–2016).
In a study focusing on Barkley Sound,
an area that comprises ∼0.3% of the
Canadian coastline on the west coast of
Vancouver Island, Starko et al. (2022)
examined local impacts to kelp (both
giant and bull kelp) during the 2014–
2016 marine heatwave. Nearly all kelp
forests persisted toward the cool outer
coast, but extensive kelp loss was
observed inshore where surface water
temperatures were >3 °C warmer. The
authors concluded that the responses of
kelp forests to warm water events are
highly variable at local scales with areas
experiencing loss only 2–3 km away
from areas where kelp was resilient.
In summary, long-term data suggest
that bull kelp populations in Canada
appear stable or increasing in most
areas, especially on the outer coast. Very
small areas that tend to be inshore and
constitute <1% of the range of the
species in Canada experienced declines
during the marine heatwave of 2014–
2016. These localized declines were not
significant enough to change the
outcome of longer-term studies that
suggest stability or increases of bull kelp
in Canada or across its range.
Washington
The petitioner states that bull kelp
decline in Washington is associated
with warmer water temperatures and
proximity to human populations (Pfister
et al. 2018). The information in our files
suggests that Puget Sound bull kelp
populations have experienced major
losses since the late 1800s; population
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declines of 96 percent and 83 percent
were reported in the Central and West
sub-basins, respectively (Berry et al.
2021). This pattern of decline did not
hold true for the Strait of Juan de Fuca
at the entrance to the Salish Sea where
the bull kelp forest has generally
remained stable over the last century,
except along the eastern boundary of the
Strait (Pfister et al. 2018). Krumhansl et
al. (2016) found no directional trend
over a 30-year time frame in the larger
ecoregion they studied, which
encompassed Washington. Furthermore,
bull kelp populations on the outer coast
of Washington have remained stable or
increased since the 1990s (Pfister et al.
2017). Berry et al. (2021) noted that
these contrasting patterns of adjacent
sub-regions experiencing loss and
stability have occurred in other
locations globally.
The petitioner does not comment
specifically about how the bull kelp
forests in Washington responded to the
marine heat wave of 2014–2016.
Information in our files suggests that
sites along Washington’s outer coast and
in the Strait of Juan de Fuca
experienced a ∼50 percent decline of
their predominantly bull kelp canopy
during the marine heat wave, but that
the canopy quickly recovered and stipe
density increased after 2015 (Tolimieri
et al. 2023). In summary, long-term data
suggest that bull kelp populations along
the outer coast of Washington and in the
Strait of Juan de Fuca (except along the
eastern boundary) are stable or
increasing following the marine heat
wave, while populations in Puget Sound
are in decline. There is no evidence
presented by the petitioners or that we
have readily available in our files that
these small areas of decline had an
impact on the status or health of the
species in Washington or throughout its
range.
Oregon
The petitioner does not specifically
mention the status of bull kelp
populations in Oregon, where bull kelp
is the dominant canopy kelp species.
Long-term data in our files suggest
variable trends between 1984–2018
according to one study (Hamilton et al.
2020) and a 0.8 percent decline between
1984–2021 according to another study
that is in review (Bell et al. in review).
Both studies found that the marine heat
wave of 2014–2016 had little effect on
bull kelp populations in Oregon, and
that bull kelp beds in Oregon appear to
be more resistant to the heat wave
events compared to other areas
(Hamilton et al. 2020, Bell et al. in
review). Resilience among the kelp beds
of Oregon was variable, but overall
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positive, between 2014–2016. In some
areas, population sizes grew to higher
levels compared to those recorded prior
to the heat wave (Rogue Reef) and others
remained stable (Orford Reef; Hamilton
et al. 2020).
In summary, long-term data suggest
that bull kelp populations in Oregon
have fluctuated over time, with periods
of stability, declines, and increases
depending on the particular area being
studied. Oregon populations also appear
to be fairly resilient to the marine heat
wave of 2014–2016.
Northern California
The petitioner cites a negative kelp
canopy population trend in Northern
and Central California from 1973–2012
and references Krumhansl et al. (2016),
who do not distinguish which kelp
species, of the 14 examined, are
responsible for the negative trend
observed. The petitioner claims that a
negative trend in multi-species (both
canopy and understory) kelp decline
indicates a species-specific decline in
bull kelp within Northern and Central
California. This claim is misleading
because there are two dominant kelp
canopy species along the Northern and
Central California coasts, and they are
not distributed evenly across this large
ecoregion. Bull kelp is the predominant
canopy forming species in Northern
California, and giant kelp is the
predominant species in Central
California. Krumhansl et al. (2016)
estimated a decline of 2% in kelp
abundance per year in this large region
that encompasses all of Northern and
Central California; however, it is not
known which species are driving the
downward trend and it is not reasonable
to assume that each canopy species
contributed to this decline equally
because they are not distributed equally
across the entire area. Bell et al. (in
review) examined trends in bull kelpdominated Northern California. They
found no significant long-term trend in
bull kelp abundance based on kelp
canopy cover from the 1980s to present
at 80 percent of the sites they studied.
They did observe large fluctuations in
kelp canopy in Northern California
throughout the time period,
emphasizing that high variability in
abundance is characteristic of bull kelp
populations in this region.
The petitioner states that there have
been alarming bull kelp population
declines since 2014 following the
marine heat wave in Sonoma and
Mendocino counties where the canopy
has declined by 90 percent and kelp
have not recovered as expected (RogersBennett & Catton 2019, Finger et al.
2021, Bell et al. in review). We have
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corroborated this claim based on the
information provided by the petitioner
and the information we have in our files
(McPherson et al. 2021, Ward et al.
2022). Bell et al. (in review) found low
resistance and resilience of bull kelp
populations in Northern California
following the marine heat wave of
2014–2016, but documented signs of
recovery began in 2021. Resistance was
defined as the degree to which bull kelp
canopy area changed during and shortly
following the marine heat wave (2014–
2016) relative to the baseline period
immediately preceding the heatwave
event (2009–2013) and resilience was
defined as the degree to which bull kelp
canopy area recovered following the
marine heat wave (2017–2021) relative
to the baseline period (Bell et al., in
review).
In summary, long-term data presented
in the petition and/or readily available
in our files suggest no significant trend
in bull kelp populations in Northern
California despite significant declines in
Sonoma and Mendocino counties
following the marine heat wave of
2014–2016. In addition, there are signs
of very slow recovery in Sonoma and
Mendocino counties beginning in 2021
(Bell et al., in review). There is no
evidence presented by the petitioners,
or that we have readily available in our
files, that the small areas of decline in
Sonoma and Mendocino counties (∼10%
of the species’ range) are having an
impact on the status or health of the
species in other areas of Northern
California or throughout the bull kelp
range.
Central California
As noted above for Northern
California, Krumhansl et al. (2016)
combined Northern and Central
California together as well as combining
trends for 14 species of kelp, both
canopy-forming and understory species,
to estimate a decline of 0.02 in kelp
abundance per year in this region
between 1973–2012. It is not known
which species are driving the
downward trend. Bull kelp is not
distributed evenly across the ecoregion
that includes both Northern and Central
California, and giant kelp is the
predominant species in Central
California. Bell et al. (in review)
examined trends in kelp canopy in
Central California from 1984–2021 and
found a decline of 0.06 percent per year,
but the authors indicate that declines in
giant kelp, not bull kelp, were primarily
responsible for driving this downward
trend. Bell et al. (in review) found that
resistance and resilience of the kelp
canopy were relatively high following
the 2014–2016 marine heat wave, but
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again there is no evidence that these
metrics can be applied to bull kelp
specifically.
In summary, the predominant canopyforming kelp in this region is giant kelp,
not bull kelp, so long-term studies of
kelp canopy in this area do not directly
inform the status of bull kelp in Central
California. The petitioners provide no
evidence, and we have no information
readily available in our files suggesting
a decline in the status of bull kelp in
Central California.
Overall Status and Trend
While the petitioner claims that
alarming declines in bull kelp
populations are occurring throughout
the species’ range, they fail to provide
substantial scientific or commercial
information indicating that bull kelp
may be declining and may warrant
listing based on status throughout all or
a significant portion of its range. Bell et
al. (in review) conclude that long-term,
continuous datasets spanning 40 years
or more are necessary to put short-term
declines in canopy kelp populations
into the context of long-term dynamics.
In addition, studies examining the
waxing and waning of bull kelp
populations at local scales and over
short periods of time (i.e., up to several
years) found that factors thought to be
responsible for declines do not operate
equally throughout the bull kelp range.
Declines occurring in a small portion of
the bull kelp range over short-term time
frames are not indicative of long-term
status across the species’ range or in a
significant portion of the range.
The data that the petitioner cites and
that we have in our files suggest stable
or increasing bull kelp populations are
present in the northern (i.e., Alaska) and
southern (i.e., Northern California)
portions of the bull kelp range, as well
as many areas in between. The areas
where bull kelp populations are stable
or increasing comprise a large
percentage of the species’ range (∼80%)
and almost all populations from Alaska
to Oregon appear to be resilient to
marine heat waves, especially the most
recent marine heatwave of 2014–2016.
In Northern California, where bull kelp
populations declined dramatically
following the 2014–2016 marine heat
wave, there is evidence of recovery
beginning in 2021.
In sum, the status of bull kelp in
geographic portions of its range
indicates that bull kelp populations are
predominantly stable or increasing
throughout the range of the species as
well as within significant portions of its
range.
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Analysis of ESA Section 4(a)(1) Factors
In the following sections, we
summarize our evaluation of the
information presented by the petition
and readily available in our files
regarding the specific ESA section
4(a)(1) factors (hereafter ‘‘listing
factors’’) that may be affecting bull
kelp’s risk of extinction.
Present or Threatened Destruction,
Modification, or Curtailment of Its
Habitat or Range
The petitioner states that climate
change, specifically warming ocean
temperatures, is the predominant threat
to bull kelp across its range. The
petitioner states that the marine heat
wave of 2013 (‘‘The Blob’’) followed by
the strong 2015/2016 El Nin˜o event
resulted in unprecedented sea surface
temperature increases that caused bull
kelp populations to crash. The
petitioner asserts that bull kelp’s
apparent failure to recover to pre-Blob
levels of canopy coverage indicates that
bull kelp lacks resilience and resistance
to temperature increases, thus providing
a snapshot into what a warmer future
looks like as climate change worsens.
However, the information provided with
the petition and in our files suggest that
as an annual species, bull kelp regularly
undergoes boom and bust cycles as part
of its life history, and therefore some
degree of fluctuation in abundance year
to year is expected. Furthermore, bull
kelp has persisted through several
intense El Nin˜o events historically. The
marine heatwave of 2014–2016 affected
bull kelp in some areas across its range,
with variability in response over small
spatial and temporal scales.
The petitioner did not present longterm trends in abundance or
distribution for bull kelp across its
entire range; they relied heavily on Bell
et al. (in review), who used land-sat
images to examine long-term trends in
kelp canopy cover (both N. luetkeana
and M. pyrifera) in regions from Oregon
to Baja California. This study found a
strong latitudinal response to the
heatwave event, with high spatial
variability in recovery that included
considerable small-scale (meters to
kilometers) local effects. Overall, in this
study, both resilience and resistance to
the heat wave increased with increasing
latitude; from Northern California to
Oregon (bull kelp dominated areas) and
Baja California Sur to Central California
(giant kelp dominated areas). In
response to the most recent heatwave
event, kelp canopies in Oregon were
highly variable, with some areas
showing less than 10% recovery and
some as high as 1,400% of baseline
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levels. Kelp forests in Northern
California exhibited historic lows
during and post-marine heatwave
(2014–2021), although no long-term
regional decline (i.e., no trend) was
detected in the overall time series
(1984–2021). In contrast, kelp forests in
Central California showed a significant
long-term regional decline, driven by
large decreases in canopy cover around
the Monterey Peninsula, where giant
kelp, not bull kelp, is the dominant
canopy species.
Other studies on kelp forests across
latitudinal gradients found increasing
temperatures did not change kelp
canopy cover biomass, but instead
showed temperature-driven alteration in
physiological performance that led to
the reduction of kelp bed resiliency. The
petitioner cites Wernberg et al. (2010),
who conducted disturbance
experiments in 24 kelp forest reefs in
four regions spanning temperatures of
2–4 °C in western Australia. In this
study, there was no significant
relationship between temperature and
kelp canopy biomass across the
temperature gradients and regions, but it
was found that kelps adjusted key
metabolic processes in response to
prevailing temperature. Physiological
performance was reduced under warmer
temperatures resulting in reduced
reproduction, recruitment, and recruit
survival compared to regions with
cooler temperatures. As a consequence
of low recruit abundance, kelp beds in
northern latitudes (warmer water) had
lower resilience to experimental
perturbations compared to southern
latitude kelp beds (colder water),
suggesting there is an interaction
between temperature regime and
intensity of disturbance. The results of
this study suggest that while kelp forest
canopies may remain intact across
latitudinal gradients, under warmer
temperatures they may be more
susceptible to other stressors like
disease, poor water quality, reduced
light levels, or physical disturbance,
thereby diminishing their capacity for
canopy regeneration in the long-term
(Wernberg et al. 2010).
Additional information present in our
files and provided by the petitioner
shows that microclimate and other local
scale effects play important roles in
mediating bull kelp resilience across its
range. A study by Starko et al. (2022) in
Barkley Sound, British Columbia, an
area that comprises ∼0.3% of the
Canadian coastline, examined the role
of fine-scale environmental variation
(i.e., microclimate) in the indirect and
direct effects of the 2014–2016 North
Pacific heatwave on the persistence of
the Pacific’s predominant canopy-
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forming species, bull kelp and giant
kelp. The authors demonstrated kelp
forests went locally extinct as a result of
the heatwave at 40 percent of the sites
surveyed in that area, with most losses
occurring at inshore sites that
experienced the warmest temperatures.
However, despite extirpation in these
inshore areas, the authors found that
kelp forests offshore persisted in deeper,
cooler, nutrient-rich waters. This
thermal refugia was limited by urchin
grazing pressure at greater depths, but it
was also found that some of the warmer
inshore areas provided refuge from
urchins depending on substrate type.
This demonstrates how microclimate
and grazing pressure may interact to
influence kelp forest occupancy in a
system, and despite warming waters,
microhabitats that support kelp forests
can still persist.
Other studies support the importance
of microclimates in driving kelp forest
dynamics. For example, Schroeder et al.
(2019) found that spatial and temporal
persistence of bull kelp along the west
coast of British Columbia varied with
the local effects of current speed,
temperature, and substrate type, with
greater persistence in areas with higher
currents and rockier substrates. BeasLuna et al. (2020) examined kelp forest
communities from Alaska to Baja
California, Mexico, and found that local
factors such as species composition,
local oceanographic conditions, and
human activities led to different
patterns of kelp forest community
response to climate change along the
west coast of North America, with
greater changes observed in the
southern portions of the range, and
more resilience in the central and
northern portions where bull kelp is the
dominant canopy forming species. In a
global review, Krumhansl et al. (2016)
analyzed global kelp forest change in
ecoregions with data from the past 50
years and also concluded that local
factors play a dominant role in driving
kelp forest dynamics. Based on the
literature in our files and provided by
the petitioner, bull kelp population
trajectories vary in direction and
magnitude among ecoregions or
microclimates rather than on broad
spatial scales, with some areas
exhibiting decline in biomass and other
areas remaining stable or even
increasing.
In summary, the information
presented by the petitioner and
literature in our files provides evidence
that warming ocean temperatures
associated with marine heatwaves and
climate change has resulted in bull kelp
decline in some spatially limited areas.
However, overall, bull kelp canopy
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recovery following warming events is
spatially variable and often driven by a
suite of local environmental factors.
According to long-term, speciesspecific, ecoregional trend data (30+
years), the best type of data for
providing insight into species resilience
over time, bull kelp is increasing or
stable in areas that span its extensive
range, including those that have been
impacted by warm-water induced
declines. Therefore, we do not find that
there is substantial information
indicating that warm water events and
climate change may be contributing to
extinction risk for the bull kelp now or
in the foreseeable future.
Overutilization for Commercial,
Recreational, Scientific or Educational
Purposes
The petitioner asserts that commercial
bull kelp harvesting threatens the
survival of bull kelp given that kelp
harvest methods can include harvesting
the upper portion of the kelp that helps
keep it buoyant. The petitioner claims
these methods can also inhibit the
capacity for reproduction. The
petitioner cites recent limits and
closures of bull kelp harvest in
California as evidence that additional
measures are needed to protect bull
kelp. Springer et al. (2010) outlines the
regulatory framework and limitations on
bull kelp harvesting in California,
Oregon, Washington, British Columbia,
and Alaska. There are restrictions or
prohibitions on commercial harvest
throughout the range of bull kelp, and
historically there has been relatively
limited commercial harvest (Springer et
al. 2010). There are also restrictions on
the harvest amount and/or allowable
location of bull kelp harvest for
personal, recreational, and scientific use
throughout California, Oregon,
Washington, British Columbia, and
Alaska, including license/permit
requirements for these non-commercial
activities in most areas (Springer et al.
2010). While the petitioner does raise
some concern about overutilization
based on the general nature of harvest,
the petitioner admits that the quantity of
harvest is not a threat, and this factor
does not appear to weigh heavily or
factor into the petitioner’s summary
explanation of why bull kelp may
warrant listing under the ESA. The
information presented in the petition
and available in our files does not
indicate that harvest for commercial,
personal, recreational, and scientific use
is a threat to bull kelp.
While not discussed or referenced by
the petitioner, information in our files
indicates that aquaculture production of
bull kelp has recently developed or is
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being actively pursued for commercial
and restoration uses in Washington and
Alaska (https://www.fisheries.noaa.gov/
national/aquaculture/seaweedaquaculture). These aquaculture
activities are closely regulated by the
states of Washington and Alaska, with
additional federal and/or local
requirements that may apply for such
facilities and operations. Bull kelp
grown in aquaculture provides some of
the ecosystem services of wild
populations such as carbon
sequestration, nitrogen removal,
providing habitat for fish, invertebrates,
and other fauna, and dissipation of
wave energy. Currently, NMFS does not
consider kelp aquaculture to be a threat
to wild populations of bull kelp.
Disease or Predation
The petitioner asserts that predation
by sea urchins poses a threat to bull
kelp. The petitioner identifies trophic
imbalances associated with the loss of
urchin predators, such as the sea otter
and sunflower sea star, as a factor that
can devastate the bull kelp ecosystem
and lead to the development of urchin
barrens. Urchin barrens may form when
urchin herbivory results in kelp
deforestation and a community
dominated by crustose coralline algae.
They assert that urchin barrens have
occurred along the North American west
coast, from north of San Francisco to the
Oregon border. Although urchin
predation has been attributed as one of
the primary stressors to kelp in
Mendocino and Sonoma counties in
Northern California, Hamilton et al.
(2020) demonstrated that Oregon bull
kelp population sizes were not
significantly affected by the increase in
urchin density that occurred in
connection with the 2014 marine heat
wave. Bull kelp have persisted in
Oregon despite the functional extinction
of sea otters and recent decline in
sunflower sea stars (Hamilton et al.
2020). Similarly, Tolmieri et al. (2023)
did not observe a strong, negative
correlation between urchins and canopy
kelp species in Washington.
The petitioner asserts that urchin
barrens may become alternate stablestates of the ecosystem in which a
return to a kelp forest state would be
difficult. Although the development of
alternate stable-states may occur, there
is significant spatiotemporal variation in
the ecological processes that sustain
such states. For example, pathogen
induced sea urchin mortality has
resulted in repeated flipping between
kelp forests and urchin barrens in Nova
Scotia. Pathogen-induced sea urchin
mortality has also been observed in
California (Steneck and Johnson, 2013).
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In addition, urchin biomass removal
due to a directed fishery or as a kelp
restoration action may shift barrens back
to kelp forest communities (Steneck and
Johnson, 2013, Williams et al. 2021,
Eger et al. 2022).
The petitioner also claims that sea
urchin predation will be worsened by
climate change due to reductions in
kelp density associated with increased
and stronger storm systems. They claim
that a decrease in kelp density would
increase predation from sea urchins.
Although strong storm events have the
potential to reduce the size of kelp
forests, bull kelp has been observed to
rapidly recolonize disturbed areas
following removal of more
competitively dominant algal species
(Springer et al., 2010). Thus, in some
cases, storm energy may have a positive
effect on bull kelp abundance. In
contrast to the above assertion, Dayton
et al. (1992) noted an increase in urchin
predation in response to the loss of drift
kelp, not a decrease in kelp density.
The petition presents credible
information that predation by sea
urchins has created barrens in some
areas. However, the long-term data
readily available in our files suggest that
bull kelp is actually increasing or stable
within regions that encompass those
smaller areas that have been impacted
by localized urchin predation.
Therefore, we conclude that the petition
does not present substantial information
indicating that disease or predation is
posing a threat to bull kelp such that it
is contributing to extinction risk.
Inadequacy of Existing Regulatory
Mechanisms
The petitioner asserts the existing
regulatory mechanisms are insufficient
to protect bull kelp from extinction and
that bull kelp does not currently hold
protected status under any
environmental law. The only regulatory
mechanism identified by the petitioner
is that provided by the National Marine
Sanctuary System, and they assert that
such protections are only provided in
the southernmost part of the bull kelp
habitat range. The petitioner incorrectly
asserts that there are no National Marine
Sanctuaries in Washington. To the
contrary, the Olympic Coast National
Marine Sanctuary includes 3,188 square
miles of marine water including the
nearshore waters off the Olympic
Peninsula in the State of Washington.
The petitioner does not specify
particular threats for which existing
regulatory mechanisms are inadequate
and does not provide substantial
scientific or commercial information to
support their assertion. Given this lack
of specificity, we note below some of
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the existing regulatory mechanisms that
address manmade factors identified
elsewhere in the petition.
Although the petitioner asserts that
bull kelp does not currently hold
protected status under any
environmental law, they note elsewhere
in the petition that the California Fish
and Game Commission approved a 3year temporary closure of bull kelp
commercial harvest off Sonoma and
Mendocino counties in California, and
limited harvest off Humboldt and Del
Norte counties. This is a regulatory
mechanism designed to protect against
an overutilization threat. We also note
that the State of California has initiated
the development of a statewide, climateready Kelp Restoration and Management
Plan for California, which will include
a harvest management framework and
other fishery management plan elements
required by the State of California’s
Marine Life Management Act, an
innovative framework for ecosystembased management of kelp forests, and
a restoration toolkit consisting of
restoration options available to resource
managers in California. In addition, as
described previously in Overutilization
for commercial, recreational, scientific
or educational purposes, there are
management frameworks for bull kelp in
place throughout its range that regulate
the harvest and/or use of bull kelp for
any purpose.
The U.S. Army Corps of Engineers
South Pacific Division also considers
kelp to be a special aquatic site (40 CFR
230 Section 404(b)(1) Guidelines). This
status provides special consideration
when evaluating permit applications for
dredged or fill material pursuant to
Section 404 of the Clean Water Act. This
is a regulatory mechanism that can
address aspects of the coastal darkening
factor identified in Other natural or
manmade factors affecting the bull
kelp’s continued existence section of the
petition. In addition, canopy kelp,
which includes bull kelp, has been
designated as essential fish habitat
(EFH) pursuant to the MagnusonStevens Fishery Conservation and
Management Act for various federally
managed fish species under the Pacific
Coast Groundfish (PCG) and Pacific
Coast Salmon (PCS) Fishery
Management Plans (FMPs). Moreover,
canopy kelp has been designated as a
habitat area of particular concern
(HAPC) for various fish species under
the PCG and PCS FMPs. Federal
agencies must consult with NMFS
regarding any proposed action that may
adversely affect EFH or a HAPC, and
must consider NMFS’s conservation
recommendations to mitigate any
environmental impacts to bull kelp
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during construction and other
development.
We conclude that the information
presented in the petition and readily
available to us does not constitute
substantial information indicating that
the inadequacies of existing regulatory
mechanisms are posing a threat to bull
kelp. To the contrary, information
readily available to us indicates a
number of existing regulatory
mechanisms which assist in kelp
protection.
Other Natural or Manmade Factors
The petitioner asserts that chemical
pollution, thermal pollution, coastal
darkening, and oil spills pose risks to
bull kelp and place the species at risk
of extinction. For example, the
petitioner expresses concern that
thermal pollution created by power
plants can jeopardize reproduction of
bull kelp. Though there are a few coastal
power plants that continue to discharge
warm water, California has established
regulations that are phasing out oncethrough cooling water for energy
production. In addition, the Diablo
Canyon power plant in central
California is currently scheduled for
decommissioning and is not anticipated
to continue discharging warm water
over the long term. San Onofre Nuclear
Generating Station (SONGS) was the
only other coastal power plant in
California that discharged warm water
in the vicinity of kelp habitat, but it is
currently being decommissioned.
Moreover, the California Coastal
Commission required SONGS to provide
compensatory mitigation for the adverse
effects to kelp and the marine
environment resulting in the largest
artificial reef project on the West Coast
of the United States. As such, it seems
that the threat of thermal pollution by
power plants has diminished
substantially and there is no indication
of that pattern reversing in the
foreseeable future.
Similar to thermal pollution, the
petitioner claims chemical pollution can
inhibit kelp reproduction, settlement,
and survival, citing evidence from
California and for other kelp species in
South America. The petition specifically
cites concerns around the impacts of
hydrazine and heavy metals on bull
kelp, pollutants emerging from coastal
factories, military bases, and airports.
However, the petition did not provide
substantial scientific or commercial
information to support these assertions,
such as documentation of existing
overlap between sources of these
chemical pollutants and bull kelp
populations and associated negative
impacts.
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Coastal darkening, defined by the
petitioner as a situation that arises when
pollutants from coastal runoff
physically block the sun, is claimed as
a stressor inhibiting bull kelp
photosynthesis, and thereby growth and
maturation, as well as bull kelp
recruitment. The evidence that coastal
darkening affects photosynthesis cited
by the petitioner is focused on a
different species of kelp, although the
petitioner does provide support for the
negative impacts of turbidity on
photosynthesis and recruitment in bull
kelp specifically. Importantly, though,
the petition does not present evidence
that human activities causing coastal
darkening within the range of bull kelp
reduce photosynthesis and recruitment
of bull kelp.
Finally, the petitioner presents
evidence from laboratory studies and
asserts that oil spills, which can expose
bull kelp to petroleum and polycyclic
aromatic hydrocarbons (PAHs) in
particular, threaten growth and
photosynthesis, thereby increasing
extinction risk. This concern is specific
to California and Alaska bull kelp
habitats where oil and gas development
occurs. While some studies have
demonstrated negative effects of
petroleum products on bull kelp,
Springer et al. (2010) indicate that little
is known about the effects of toxicants
such as oil on bull kelp. For example,
studies focused on the Exxon Valdez oil
spill in Alaska compared bull kelp
biomass and percent cover between
oiled and control sites in Prince William
Sound and found no evidence of
detrimental effects of oil exposure
(Springer et al. 2010). While oil spills
are a threat to coastal ecosystems, the
petition fails to present credible
scientific or commercial information
indicating that these forms of pollution
are posing a threat to bull kelp.
Petition Finding
In conclusion, after reviewing the
petition, the literature cited in the
petition, and other information readily
available in our files, we do not find
there is substantial information
indicating that bull kelp is declining
throughout all or a significant portion of
its range or that it is affected by threats
throughout all or a significant portion of
its range such that listing may be
warranted. We therefore conclude the
petition does not present substantial
scientific or commercial information
indicating that the petitioned action to
list N. luetkeana as a threatened or
endangered species may be warranted.
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References Cited
A complete list of all references cited
herein is available upon request (See
FOR FURTHER INFORMATION CONTACT).
Authority: The authority for this
action is the Endangered Species Act of
1973, as amended (16 U.S.C. 1531 et
seq.).
Dated: June 14, 2023.
Samuel D. Rauch, III,
Deputy Assistant Administrator for
Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. 2023–13277 Filed 6–21–23; 8:45 am]
BILLING CODE 3510–22–P
COMMODITY FUTURES TRADING
COMMISSION
Market Risk Advisory Committee;
Meeting
Commodity Futures Trading
Commission.
ACTION: Notice of meeting.
AGENCY:
The Commodity Futures
Trading Commission (CFTC) announces
that on July 10, 2023, from 10 a.m. to
1 p.m. (Eastern Daylight Time), the
Market Risk Advisory Committee
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this meeting, the MRAC will discuss
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reform, market structure, climate-related
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DATES: The meeting will be held on July
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meeting may end early if the MRAC has
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public who wish to submit written
statements in connection with the
meeting should submit them by July 17,
2023.
ADDRESSES: The meeting will be held
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public comments, identified by ‘‘Market
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comments.cftc.gov. Follow the
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Federal Officer, via the contact
information listed below to discuss
alternate means of submitting your
comments. Any statements submitted in
connection with the committee meeting
SUMMARY:
E:\FR\FM\22JNN1.SGM
22JNN1
Agencies
[Federal Register Volume 88, Number 119 (Thursday, June 22, 2023)]
[Notices]
[Pages 40782-40789]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-13277]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
[Docket No. 230613-0148; RTID 0648-XR128]
Endangered and Threatened Wildlife; 90-Day Finding on a Petition
To List the Bull Kelp as Threatened or Endangered Under the Endangered
Species Act
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; 90-day petition finding.
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SUMMARY: We, NMFS, announce a 90-day finding on a petition to list the
bull kelp (Nereocystis luetkeana) as threatened or endangered under the
Endangered Species Act (ESA) and to designate critical habitat
concurrent with the listing. We have reviewed the information presented
in the petition as well as information readily available in our files
and find that the petition does not present substantial scientific or
commercial information indicating that the petitioned actions may be
warranted. Therefore, we are denying this petition.
ADDRESSES: Interested persons may obtain a copy of the petition online
at the NMFS website: https://www.fisheries.noaa.gov/national/endangered-species-conservation/negative-90-day-findings.
FOR FURTHER INFORMATION CONTACT: Melissa Neuman, NMFS West Coast
Region, Protected Resources Division, (562) 481-4594,
[email protected].
SUPPLEMENTARY INFORMATION:
Background
On September 1, 2022, we received a petition from the Center for
Biological Diversity to list the bull kelp (Nereocystis luetkeana) as a
threatened or endangered species under the ESA and to designate
critical habitat concurrent with the listing. The petition asserts that
the bull kelp is threatened by all of the ESA section 4(a)(1) factors:
(1) the present or threatened destruction, modification, or curtailment
of its habitat or range; (2) overutilization for commercial,
recreational, scientific or educational purposes; (3) disease or
predation; (4) the inadequacy of existing regulatory mechanisms; and
(5) other natural or manmade factors affecting its continued existence.
The petition is available online (see ADDRESSES).
ESA Statutory, Regulatory, and Policy Provisions and Evaluation
Framework
Section 4(b)(3)(A) of the ESA of 1973, as amended (16 U.S.C. 1531
et seq.), requires, to the maximum extent practicable, that within 90
days of receipt of a petition to list a species as threatened or
endangered, the Secretary of Commerce shall make a finding on whether
that petition presents substantial scientific or commercial information
indicating that the petitioned action may be warranted, and promptly
publish such finding in the Federal Register (16 U.S.C. 1533(b)(3)(A)).
If NMFS finds that substantial scientific or commercial information in
a petition indicates the petitioned action may be warranted (a
``positive 90-day finding''), we are required to promptly commence a
review of the status of the species concerned, during which we will
conduct a comprehensive review of the best available scientific and
commercial data. We conclude the review with a finding as to whether,
in fact, the petitioned action is warranted within 12 months of receipt
of the petition. Because the finding at the 12-month stage is based on
a more thorough review of the best available information, as compared
to the narrow scope of review at the 90-day stage, a ``positive 90-
day'' finding does not prejudge the outcome of the status review.
Under the ESA, a listing determination may address a species, which
is defined to also include subspecies and, for any vertebrate species,
any distinct population segment (DPS) that interbreeds when mature (16
U.S.C. 1532(16)). A species, subspecies, or DPS is ``endangered'' if it
is in danger of extinction throughout all or a significant portion of
its range, and ``threatened'' if it is likely to become endangered
within the foreseeable future throughout all or a significant portion
of its range (16 U.S.C. 1532(6) and (20)). Pursuant to the ESA and our
implementing regulations, we determine whether species are threatened
or endangered based on any one or a combination of the following five
ESA section 4(a)(1) factors: (1) the present or threatened destruction,
modification, or curtailment of its habitat or range; (2)
overutilization for commercial, recreational, scientific, or
educational purposes; (3) disease or predation; (4) the inadequacy of
existing regulatory mechanisms; and (5) other natural or manmade
factors affecting its continued existence (16 U.S.C. 1533(a)(1); 50 CFR
424.11(c)).
ESA-implementing regulations issued jointly by NMFS and the U.S.
Fish and
[[Page 40783]]
Wildlife Service (50 CFR 424.14(h)(1)(i)) define ``substantial
scientific or commercial information'' in the context of reviewing a
petition to list, delist, or reclassify a species as credible
scientific or commercial information in support of the petitioner's
claims such that a reasonable person conducting an impartial scientific
review would conclude that the action proposed in the petition may be
warranted. Conclusions drawn in the petition without the support of
credible scientific or commercial information will not be considered
substantial information. In reaching the 90-day finding on the
petition, we considered the information described in sections 50 CFR
424.14(c) and (d).
Our determination as to whether the petition provides substantial
scientific or commercial information indicating that the petitioned
action may be warranted depends in part on the degree to which the
petition includes the following types of information: (1) information
on current population status and trends and estimates of current
population sizes and distributions, both in captivity and the wild, if
available; (2) identification of the factors under section 4(a)(1) of
the ESA that may affect the species and where these factors are acting
upon the species; (3) whether, and to what extent, any or all of the
factors alone or in combination identified in section 4(a)(1) of the
ESA may cause the species to be an endangered species or threatened
species (i.e., the species is currently in danger of extinction or is
likely to become so within the foreseeable future), and, if so, how
high in magnitude and how imminent the threats to the species and its
habitat are; (4) information on adequacy of regulatory protections and
effectiveness of conservation activities by States, as well as other
parties, that have been initiated or that are ongoing, that may protect
the species or its habitat; and (5) a complete, balanced representation
of the relevant facts, including information that may contradict claims
in the petition. See 50 CFR 424.14(d).
If the petitioner provides supplemental information before the
initial finding is made and states that it is part of the petition, the
new information, along with the previously submitted information, is
treated as a new petition that supersedes the original petition, and
the statutory timeframes will begin when such supplemental information
is received. See 50 CFR 424.14(g).
We may also consider information readily available at the time the
determination is made (50 CFR 424.14(h)(1)(ii)). We are not required to
consider any supporting materials cited by the petitioner if the
petitioner does not provide electronic or hard copies, to the extent
permitted by U.S. copyright law, or appropriate excerpts or quotations
from those materials (e.g., publications, maps, reports, letters from
authorities). See 50 CFR 424.14(c)(6); 424.14(h)(1)(ii).
The substantial scientific or commercial information standard must
be applied in light of any prior reviews or findings we have made on
the listing status of the species that is the subject of the petition
(50 CFR 424.14(h)(1)(iii)). Where we have already conducted a finding
on, or review of, the listing status of that species (whether in
response to a petition or on our own initiative), we will evaluate any
petition received thereafter seeking to list, delist, or reclassify
that species to determine whether a reasonable person conducting an
impartial scientific review would conclude that the action proposed in
the petition may be warranted despite the previous review or finding.
Where the prior review resulted in a final agency action--such as a
final listing determination, a 90-day not-substantial finding, or a 12-
month not-warranted finding--a petition will generally not be
considered to present substantial scientific and commercial information
indicating that the petitioned action may be warranted unless the
petition provides new information or analysis not previously
considered. 50 CFR 424.14(h)(1)(iii).
At the 90-day finding stage, we do not conduct additional research
and we do not solicit information from parties outside the agency to
help us in evaluating the petition. We accept the petitioner's sources
and characterizations of the information presented if they appear to be
based on accepted scientific principles, unless we have specific
information in our files that indicates the petition's information is
incorrect, unreliable, obsolete, or otherwise irrelevant to the
requested action. Information that is susceptible to more than one
interpretation, or that is contradicted by other available information,
will not be dismissed at the 90-day finding stage, so long as it is
reliable and a reasonable person conducting an impartial scientific
review would conclude it supports the petitioner's assertions. In other
words, conclusive information indicating the species may meet the ESA's
requirements for listing is not required to make a positive 90-day
finding. We will not conclude that a lack of specific information alone
necessitates a negative 90-day finding if a reasonable person
conducting an impartial scientific review would conclude that the
unknown information itself suggests the species may be at risk of
extinction presently or within the foreseeable future.
To make a 90-day finding on a petition to list a species, we
evaluate whether the petition presents substantial scientific or
commercial information indicating the subject species may be either a
threatened or endangered species, as defined by the ESA. First, we
evaluate whether the information presented in the petition, in light of
the information readily available in our files, indicates that the
petitioned entity constitutes a ``species'' eligible for listing under
the ESA. Next, we evaluate whether the information indicates that the
species faces an extinction risk such that listing may be warranted;
this may be indicated in information expressly discussing the species'
status and trends, or in information describing impacts and threats to
the species. We evaluate whether the petition presents any information
on specific demographic factors pertinent to evaluating extinction risk
for the species (e.g., population abundance and trends, productivity,
spatial structure, age structure, sex ratio, diversity, current and
historical range, habitat integrity or fragmentation), and the
potential contribution of identified demographic risks to extinction
risk for the species. We then evaluate whether the petition presents
information suggesting potential links between these demographic risks
and the causative impacts and threats identified in section 4(a)(1) of
the ESA.
Information presented on impacts or threats should be specific to
the species and should reasonably suggest that one or more of these
factors may be operative threats that act, or have acted, on the
species to the point that it may warrant protection under the ESA.
Broad statements about generalized threats to the species, or
identification of factors that could negatively impact a species, do
not constitute substantial information indicating that listing may be
warranted. We look for information indicating that not only is the
particular species exposed to a factor, but that the species may be
responding in a negative fashion. We then assess the potential
significance of that negative response.
Many petitions identify risk classifications made by
nongovernmental organizations, such as the International Union for
Conservation of Nature (IUCN), the American Fisheries Society, or
NatureServe, as evidence of extinction risk for a species. Risk
classifications by
[[Page 40784]]
other organizations or made under other Federal or State statutes may
be informative, but such classification alone may not provide the
rationale for a positive 90-day finding under the ESA. For example, as
explained by NatureServe, their assessments of a species' conservation
status do ``not constitute a recommendation by NatureServe for listing
under the U.S. Endangered Species Act'' because NatureServe assessments
``have different criteria, evidence requirements, purposes and
taxonomic coverage than government lists of endangered and threatened
species, and therefore these two types of lists should not be expected
to coincide'' (https://explorer.natureserve.org/AboutTheData/DataTypes/ConservationStatusCategories). Additionally, species classifications
under IUCN and the ESA are not equivalent; data standards, criteria
used to evaluate species, and treatment of uncertainty are also not
necessarily the same. Thus, when a petition cites such classifications,
we will evaluate the source of information that the classification is
based upon in light of the standards on extinction risk and impacts or
threats discussed above.
Taxonomy
Bull kelp, Nereocystis luetkeana, is a large brown alga in the
kingdom Chromista (single-celled and multicellular eukaryotes with
photosynthetic plastid organelles), phylum Gyrista, class Phaeophyceae
(brown algae), and order Laminariales (the true kelps). Laminariales
contains three families: Alariaceae, Laminariaceae, and Lessoniaceae.
Traditional taxonomy, largely based on sporophyte morphology, was used
to differentiate the brown algae and resulted in the placement of bull
kelp into the family Lessoniaceae (Springer et al. 2007). In recent
years, molecular techniques and resulting genetic data have challenged
traditional taxonomy within the order resulting in a taxonomic revision
at the family level based on evolutionary relationships (Lane et al.
2006). Bull kelp is now in the family Laminariaceae, not Lessoniaceae
as the petitioner stated, and it is the only species within its genus,
Nereocystis.
Distribution, Habitat, and Life History
Bull kelp is an annual marine macroalgal species that attaches to
rocky substrates using its holdfast in intertidal and subtidal coastal
habitats in the Northeastern Pacific Ocean from the Aleutian Islands,
Alaska, to Santa Barbara County, California (Springer et al. 2010).
Bull kelp typically occupies turbulent habitats between 3-20 m depth,
and it can co-occur with other large brown kelps including dragon kelp
(Eularia fistulosa) and giant kelp (Macrocystis pyrifera). It is
considered to be a foundational species because it provides habitat for
a variety of other marine organisms.
Bull kelp reproduces sexually. Adults, also known as sporophytes,
become mature during the summer or fall seasons at which time patches
of spores, called sori, form on the kelp blades. Sori are shed around
dawn and are negatively buoyant, causing them to sink. The sori release
individual spores into the water column as they sink and upon reaching
the substrate for up to approximately four hours. During this stage,
both sori and spores have the capacity for dispersal, but the temporal
and spatial scale of dispersal has not been quantified to date
(Springer et al. 2010). Spores have limited ability to photosynthesize
and therefore are likely not adapted for a long planktonic life. Given
the suspected limited dispersal distances, spores are thought to settle
near adults. Individual sporophytes have the ability to produce and
release sori in pulses that occur every 4-6 days with a periodicity
that varies by geographic location.
Spores that successfully settle germinate into microscopic,
sessile, male or female gametophytes. It is uncertain how long the
gametophyte stage persists and the length of the stage is likely
affected by abiotic conditions such as light, nutrients, and storm
events (Springer et al. 2007). Based on laboratory studies, gamete
production by gametophytes occurs at water temperatures between 5-15
[deg]C, but when temperatures are sustained at greater than 20 [deg]C,
morphological abnormalities in gametophytes and gametes are observed
(Vadas 1972). Prevailing knowledge suggests that male gametophytes
fertilize the female gametophytes in the winter. Increased proximity of
male and female gametophytes increases fertilization success as does a
pheromone released by female gametophytes known as lamoxirene.
Fertilized eggs begin to grow into sporophytes in the spring as
sunlight hours increase (Maier and Muller 1986). As the spring growing
season progresses, macroscopic sporophytes can grow between 6-15 cm per
day until the blades reach the water surface during the summer months
(Springer et al. 2010 referencing Scagel 1946, Lindeberg and Lindstrom
2010). At this point, growth slows and the sporophyte diverts its
energy to producing spores. Typically, the life of an individual
sporophyte ends at this point, but Springer (2010) referring to
(Chenelot et al. 2001) points out that individuals produced late in the
season in shallow water or wave-protected areas may successfully
overwinter and survive a second year.
Status and Population Trends
Alaska
The petitioner cites Krumhansl et al. (2016) when stating that
population trends of kelp are negative in the Aleutian Islands and that
bull kelp is the primary kelp species in this region. We did not find
evidence that Krumhansl et al. (2016) identified bull kelp as the
primary kelp species in the ecoregion that they refer to as the
Aleutian Islands. The authors examined an overall trend for eight
species, including bull kelp, but did not identify species-specific
trends. Information provided by the petitioner (PNW Herbaria Map,
Springer et al. 2010) and readily available in our files suggests that
bull kelp occurs in an area that constitutes less than a third of the
Aleutian Island chain and bull kelp does not occur west of the Samalga
Pass, a natural, historic biogeographic barrier to bull kelp
colonization (Konar et al. 2017). Throughout the remaining two thirds
of the Aleutian Island chain, dragon kelp, Eualaria fistulosa, is the
dominant kelp canopy species and it was part of the species complex
examined is the Aleutian Islands ecoregion by Krumhansl et al. (2016).
Therefore, the petitioners are incorrect in suggesting that the long-
term trend observed for the Aleutian Island ecoregion is due to bull
kelp declines.
Krumhansl et al. (2016) inferred relatively high magnitude
increases in kelp abundance for the Gulf of Alaska and the North
American Pacific Fjordland. Bull kelp is the dominant kelp canopy
species in these regions, occurring throughout both regions with no
major breaks in distribution (https://www.shorezone.org/). In this
case, it is reasonable to assume that bull kelp contributed
significantly to increasing long-term trends observed by Krumhansl et
al. (2016).
In summary, the overall status of bull kelp in Alaska indicates
that populations have increased along the portion of the coastline
where bull kelp occurrence is consistent and known (Gulf of Alaska and
the North American Pacific Fjordland; Krumhansl et al. 2016). In the
Aleutian Islands, where bull kelp is not a primary kelp species and has
only been observed in an area that comprises <33% of the ecoregion,
long-term trends remain uncertain.
[[Page 40785]]
Canada
The literature cited in the petition and the information we have
readily available in our files present limited evidence of bull kelp
decline in Canadian waters based on long-term trend studies conducted
off the West Coast of North America. Krumhansl et al. (2016) inferred
relatively high magnitude increases in kelp abundance for the North
American Pacific Fjordland from 1983-2012, and it is reasonable to
assume that bull kelp contributed to this increasing trend because it
occurs throughout the ecoregion with no breaks in its distribution.
Schroeder et al. (2019) found limited evidence of bull kelp decline in
British Columbia from 2004-2017, a time period that pre-dates and
follows the marine heat wave of 2014-2016. In a shorter-term study
along the central coast of British Columbia, Burt et al. (2018) found
fluctuating kelp canopy cover that may have been related to predator/
prey interactions and found no evidence for kelp decline over the time
period they examined (2006, 2012, 2014-2016).
In a study focusing on Barkley Sound, an area that comprises ~0.3%
of the Canadian coastline on the west coast of Vancouver Island, Starko
et al. (2022) examined local impacts to kelp (both giant and bull kelp)
during the 2014-2016 marine heatwave. Nearly all kelp forests persisted
toward the cool outer coast, but extensive kelp loss was observed
inshore where surface water temperatures were >3 [deg]C warmer. The
authors concluded that the responses of kelp forests to warm water
events are highly variable at local scales with areas experiencing loss
only 2-3 km away from areas where kelp was resilient.
In summary, long-term data suggest that bull kelp populations in
Canada appear stable or increasing in most areas, especially on the
outer coast. Very small areas that tend to be inshore and constitute
<1% of the range of the species in Canada experienced declines during
the marine heatwave of 2014-2016. These localized declines were not
significant enough to change the outcome of longer-term studies that
suggest stability or increases of bull kelp in Canada or across its
range.
Washington
The petitioner states that bull kelp decline in Washington is
associated with warmer water temperatures and proximity to human
populations (Pfister et al. 2018). The information in our files
suggests that Puget Sound bull kelp populations have experienced major
losses since the late 1800s; population declines of 96 percent and 83
percent were reported in the Central and West sub-basins, respectively
(Berry et al. 2021). This pattern of decline did not hold true for the
Strait of Juan de Fuca at the entrance to the Salish Sea where the bull
kelp forest has generally remained stable over the last century, except
along the eastern boundary of the Strait (Pfister et al. 2018).
Krumhansl et al. (2016) found no directional trend over a 30-year time
frame in the larger ecoregion they studied, which encompassed
Washington. Furthermore, bull kelp populations on the outer coast of
Washington have remained stable or increased since the 1990s (Pfister
et al. 2017). Berry et al. (2021) noted that these contrasting patterns
of adjacent sub-regions experiencing loss and stability have occurred
in other locations globally.
The petitioner does not comment specifically about how the bull
kelp forests in Washington responded to the marine heat wave of 2014-
2016. Information in our files suggests that sites along Washington's
outer coast and in the Strait of Juan de Fuca experienced a ~50 percent
decline of their predominantly bull kelp canopy during the marine heat
wave, but that the canopy quickly recovered and stipe density increased
after 2015 (Tolimieri et al. 2023). In summary, long-term data suggest
that bull kelp populations along the outer coast of Washington and in
the Strait of Juan de Fuca (except along the eastern boundary) are
stable or increasing following the marine heat wave, while populations
in Puget Sound are in decline. There is no evidence presented by the
petitioners or that we have readily available in our files that these
small areas of decline had an impact on the status or health of the
species in Washington or throughout its range.
Oregon
The petitioner does not specifically mention the status of bull
kelp populations in Oregon, where bull kelp is the dominant canopy kelp
species. Long-term data in our files suggest variable trends between
1984-2018 according to one study (Hamilton et al. 2020) and a 0.8
percent decline between 1984-2021 according to another study that is in
review (Bell et al. in review). Both studies found that the marine heat
wave of 2014-2016 had little effect on bull kelp populations in Oregon,
and that bull kelp beds in Oregon appear to be more resistant to the
heat wave events compared to other areas (Hamilton et al. 2020, Bell et
al. in review). Resilience among the kelp beds of Oregon was variable,
but overall positive, between 2014-2016. In some areas, population
sizes grew to higher levels compared to those recorded prior to the
heat wave (Rogue Reef) and others remained stable (Orford Reef;
Hamilton et al. 2020).
In summary, long-term data suggest that bull kelp populations in
Oregon have fluctuated over time, with periods of stability, declines,
and increases depending on the particular area being studied. Oregon
populations also appear to be fairly resilient to the marine heat wave
of 2014-2016.
Northern California
The petitioner cites a negative kelp canopy population trend in
Northern and Central California from 1973-2012 and references Krumhansl
et al. (2016), who do not distinguish which kelp species, of the 14
examined, are responsible for the negative trend observed. The
petitioner claims that a negative trend in multi-species (both canopy
and understory) kelp decline indicates a species-specific decline in
bull kelp within Northern and Central California. This claim is
misleading because there are two dominant kelp canopy species along the
Northern and Central California coasts, and they are not distributed
evenly across this large ecoregion. Bull kelp is the predominant canopy
forming species in Northern California, and giant kelp is the
predominant species in Central California. Krumhansl et al. (2016)
estimated a decline of 2% in kelp abundance per year in this large
region that encompasses all of Northern and Central California;
however, it is not known which species are driving the downward trend
and it is not reasonable to assume that each canopy species contributed
to this decline equally because they are not distributed equally across
the entire area. Bell et al. (in review) examined trends in bull kelp-
dominated Northern California. They found no significant long-term
trend in bull kelp abundance based on kelp canopy cover from the 1980s
to present at 80 percent of the sites they studied. They did observe
large fluctuations in kelp canopy in Northern California throughout the
time period, emphasizing that high variability in abundance is
characteristic of bull kelp populations in this region.
The petitioner states that there have been alarming bull kelp
population declines since 2014 following the marine heat wave in Sonoma
and Mendocino counties where the canopy has declined by 90 percent and
kelp have not recovered as expected (Rogers-Bennett & Catton 2019,
Finger et al. 2021, Bell et al. in review). We have
[[Page 40786]]
corroborated this claim based on the information provided by the
petitioner and the information we have in our files (McPherson et al.
2021, Ward et al. 2022). Bell et al. (in review) found low resistance
and resilience of bull kelp populations in Northern California
following the marine heat wave of 2014-2016, but documented signs of
recovery began in 2021. Resistance was defined as the degree to which
bull kelp canopy area changed during and shortly following the marine
heat wave (2014-2016) relative to the baseline period immediately
preceding the heatwave event (2009-2013) and resilience was defined as
the degree to which bull kelp canopy area recovered following the
marine heat wave (2017-2021) relative to the baseline period (Bell et
al., in review).
In summary, long-term data presented in the petition and/or readily
available in our files suggest no significant trend in bull kelp
populations in Northern California despite significant declines in
Sonoma and Mendocino counties following the marine heat wave of 2014-
2016. In addition, there are signs of very slow recovery in Sonoma and
Mendocino counties beginning in 2021 (Bell et al., in review). There is
no evidence presented by the petitioners, or that we have readily
available in our files, that the small areas of decline in Sonoma and
Mendocino counties (~10% of the species' range) are having an impact on
the status or health of the species in other areas of Northern
California or throughout the bull kelp range.
Central California
As noted above for Northern California, Krumhansl et al. (2016)
combined Northern and Central California together as well as combining
trends for 14 species of kelp, both canopy-forming and understory
species, to estimate a decline of 0.02 in kelp abundance per year in
this region between 1973-2012. It is not known which species are
driving the downward trend. Bull kelp is not distributed evenly across
the ecoregion that includes both Northern and Central California, and
giant kelp is the predominant species in Central California. Bell et
al. (in review) examined trends in kelp canopy in Central California
from 1984-2021 and found a decline of 0.06 percent per year, but the
authors indicate that declines in giant kelp, not bull kelp, were
primarily responsible for driving this downward trend. Bell et al. (in
review) found that resistance and resilience of the kelp canopy were
relatively high following the 2014-2016 marine heat wave, but again
there is no evidence that these metrics can be applied to bull kelp
specifically.
In summary, the predominant canopy-forming kelp in this region is
giant kelp, not bull kelp, so long-term studies of kelp canopy in this
area do not directly inform the status of bull kelp in Central
California. The petitioners provide no evidence, and we have no
information readily available in our files suggesting a decline in the
status of bull kelp in Central California.
Overall Status and Trend
While the petitioner claims that alarming declines in bull kelp
populations are occurring throughout the species' range, they fail to
provide substantial scientific or commercial information indicating
that bull kelp may be declining and may warrant listing based on status
throughout all or a significant portion of its range. Bell et al. (in
review) conclude that long-term, continuous datasets spanning 40 years
or more are necessary to put short-term declines in canopy kelp
populations into the context of long-term dynamics. In addition,
studies examining the waxing and waning of bull kelp populations at
local scales and over short periods of time (i.e., up to several years)
found that factors thought to be responsible for declines do not
operate equally throughout the bull kelp range. Declines occurring in a
small portion of the bull kelp range over short-term time frames are
not indicative of long-term status across the species' range or in a
significant portion of the range.
The data that the petitioner cites and that we have in our files
suggest stable or increasing bull kelp populations are present in the
northern (i.e., Alaska) and southern (i.e., Northern California)
portions of the bull kelp range, as well as many areas in between. The
areas where bull kelp populations are stable or increasing comprise a
large percentage of the species' range (~80%) and almost all
populations from Alaska to Oregon appear to be resilient to marine heat
waves, especially the most recent marine heatwave of 2014-2016. In
Northern California, where bull kelp populations declined dramatically
following the 2014-2016 marine heat wave, there is evidence of recovery
beginning in 2021.
In sum, the status of bull kelp in geographic portions of its range
indicates that bull kelp populations are predominantly stable or
increasing throughout the range of the species as well as within
significant portions of its range.
Analysis of ESA Section 4(a)(1) Factors
In the following sections, we summarize our evaluation of the
information presented by the petition and readily available in our
files regarding the specific ESA section 4(a)(1) factors (hereafter
``listing factors'') that may be affecting bull kelp's risk of
extinction.
Present or Threatened Destruction, Modification, or Curtailment of Its
Habitat or Range
The petitioner states that climate change, specifically warming
ocean temperatures, is the predominant threat to bull kelp across its
range. The petitioner states that the marine heat wave of 2013 (``The
Blob'') followed by the strong 2015/2016 El Ni[ntilde]o event resulted
in unprecedented sea surface temperature increases that caused bull
kelp populations to crash. The petitioner asserts that bull kelp's
apparent failure to recover to pre-Blob levels of canopy coverage
indicates that bull kelp lacks resilience and resistance to temperature
increases, thus providing a snapshot into what a warmer future looks
like as climate change worsens. However, the information provided with
the petition and in our files suggest that as an annual species, bull
kelp regularly undergoes boom and bust cycles as part of its life
history, and therefore some degree of fluctuation in abundance year to
year is expected. Furthermore, bull kelp has persisted through several
intense El Ni[ntilde]o events historically. The marine heatwave of
2014-2016 affected bull kelp in some areas across its range, with
variability in response over small spatial and temporal scales.
The petitioner did not present long-term trends in abundance or
distribution for bull kelp across its entire range; they relied heavily
on Bell et al. (in review), who used land-sat images to examine long-
term trends in kelp canopy cover (both N. luetkeana and M. pyrifera) in
regions from Oregon to Baja California. This study found a strong
latitudinal response to the heatwave event, with high spatial
variability in recovery that included considerable small-scale (meters
to kilometers) local effects. Overall, in this study, both resilience
and resistance to the heat wave increased with increasing latitude;
from Northern California to Oregon (bull kelp dominated areas) and Baja
California Sur to Central California (giant kelp dominated areas). In
response to the most recent heatwave event, kelp canopies in Oregon
were highly variable, with some areas showing less than 10% recovery
and some as high as 1,400% of baseline
[[Page 40787]]
levels. Kelp forests in Northern California exhibited historic lows
during and post-marine heatwave (2014-2021), although no long-term
regional decline (i.e., no trend) was detected in the overall time
series (1984-2021). In contrast, kelp forests in Central California
showed a significant long-term regional decline, driven by large
decreases in canopy cover around the Monterey Peninsula, where giant
kelp, not bull kelp, is the dominant canopy species.
Other studies on kelp forests across latitudinal gradients found
increasing temperatures did not change kelp canopy cover biomass, but
instead showed temperature-driven alteration in physiological
performance that led to the reduction of kelp bed resiliency. The
petitioner cites Wernberg et al. (2010), who conducted disturbance
experiments in 24 kelp forest reefs in four regions spanning
temperatures of 2-4 [deg]C in western Australia. In this study, there
was no significant relationship between temperature and kelp canopy
biomass across the temperature gradients and regions, but it was found
that kelps adjusted key metabolic processes in response to prevailing
temperature. Physiological performance was reduced under warmer
temperatures resulting in reduced reproduction, recruitment, and
recruit survival compared to regions with cooler temperatures. As a
consequence of low recruit abundance, kelp beds in northern latitudes
(warmer water) had lower resilience to experimental perturbations
compared to southern latitude kelp beds (colder water), suggesting
there is an interaction between temperature regime and intensity of
disturbance. The results of this study suggest that while kelp forest
canopies may remain intact across latitudinal gradients, under warmer
temperatures they may be more susceptible to other stressors like
disease, poor water quality, reduced light levels, or physical
disturbance, thereby diminishing their capacity for canopy regeneration
in the long-term (Wernberg et al. 2010).
Additional information present in our files and provided by the
petitioner shows that microclimate and other local scale effects play
important roles in mediating bull kelp resilience across its range. A
study by Starko et al. (2022) in Barkley Sound, British Columbia, an
area that comprises ~0.3% of the Canadian coastline, examined the role
of fine-scale environmental variation (i.e., microclimate) in the
indirect and direct effects of the 2014-2016 North Pacific heatwave on
the persistence of the Pacific's predominant canopy-forming species,
bull kelp and giant kelp. The authors demonstrated kelp forests went
locally extinct as a result of the heatwave at 40 percent of the sites
surveyed in that area, with most losses occurring at inshore sites that
experienced the warmest temperatures. However, despite extirpation in
these inshore areas, the authors found that kelp forests offshore
persisted in deeper, cooler, nutrient-rich waters. This thermal refugia
was limited by urchin grazing pressure at greater depths, but it was
also found that some of the warmer inshore areas provided refuge from
urchins depending on substrate type. This demonstrates how microclimate
and grazing pressure may interact to influence kelp forest occupancy in
a system, and despite warming waters, microhabitats that support kelp
forests can still persist.
Other studies support the importance of microclimates in driving
kelp forest dynamics. For example, Schroeder et al. (2019) found that
spatial and temporal persistence of bull kelp along the west coast of
British Columbia varied with the local effects of current speed,
temperature, and substrate type, with greater persistence in areas with
higher currents and rockier substrates. Beas-Luna et al. (2020)
examined kelp forest communities from Alaska to Baja California,
Mexico, and found that local factors such as species composition, local
oceanographic conditions, and human activities led to different
patterns of kelp forest community response to climate change along the
west coast of North America, with greater changes observed in the
southern portions of the range, and more resilience in the central and
northern portions where bull kelp is the dominant canopy forming
species. In a global review, Krumhansl et al. (2016) analyzed global
kelp forest change in ecoregions with data from the past 50 years and
also concluded that local factors play a dominant role in driving kelp
forest dynamics. Based on the literature in our files and provided by
the petitioner, bull kelp population trajectories vary in direction and
magnitude among ecoregions or microclimates rather than on broad
spatial scales, with some areas exhibiting decline in biomass and other
areas remaining stable or even increasing.
In summary, the information presented by the petitioner and
literature in our files provides evidence that warming ocean
temperatures associated with marine heatwaves and climate change has
resulted in bull kelp decline in some spatially limited areas. However,
overall, bull kelp canopy recovery following warming events is
spatially variable and often driven by a suite of local environmental
factors. According to long-term, species-specific, ecoregional trend
data (30+ years), the best type of data for providing insight into
species resilience over time, bull kelp is increasing or stable in
areas that span its extensive range, including those that have been
impacted by warm-water induced declines. Therefore, we do not find that
there is substantial information indicating that warm water events and
climate change may be contributing to extinction risk for the bull kelp
now or in the foreseeable future.
Overutilization for Commercial, Recreational, Scientific or Educational
Purposes
The petitioner asserts that commercial bull kelp harvesting
threatens the survival of bull kelp given that kelp harvest methods can
include harvesting the upper portion of the kelp that helps keep it
buoyant. The petitioner claims these methods can also inhibit the
capacity for reproduction. The petitioner cites recent limits and
closures of bull kelp harvest in California as evidence that additional
measures are needed to protect bull kelp. Springer et al. (2010)
outlines the regulatory framework and limitations on bull kelp
harvesting in California, Oregon, Washington, British Columbia, and
Alaska. There are restrictions or prohibitions on commercial harvest
throughout the range of bull kelp, and historically there has been
relatively limited commercial harvest (Springer et al. 2010). There are
also restrictions on the harvest amount and/or allowable location of
bull kelp harvest for personal, recreational, and scientific use
throughout California, Oregon, Washington, British Columbia, and
Alaska, including license/permit requirements for these non-commercial
activities in most areas (Springer et al. 2010). While the petitioner
does raise some concern about overutilization based on the general
nature of harvest, the petitioner admits that the quantity of harvest
is not a threat, and this factor does not appear to weigh heavily or
factor into the petitioner's summary explanation of why bull kelp may
warrant listing under the ESA. The information presented in the
petition and available in our files does not indicate that harvest for
commercial, personal, recreational, and scientific use is a threat to
bull kelp.
While not discussed or referenced by the petitioner, information in
our files indicates that aquaculture production of bull kelp has
recently developed or is
[[Page 40788]]
being actively pursued for commercial and restoration uses in
Washington and Alaska (https://www.fisheries.noaa.gov/national/aquaculture/seaweed-aquaculture). These aquaculture activities are
closely regulated by the states of Washington and Alaska, with
additional federal and/or local requirements that may apply for such
facilities and operations. Bull kelp grown in aquaculture provides some
of the ecosystem services of wild populations such as carbon
sequestration, nitrogen removal, providing habitat for fish,
invertebrates, and other fauna, and dissipation of wave energy.
Currently, NMFS does not consider kelp aquaculture to be a threat to
wild populations of bull kelp.
Disease or Predation
The petitioner asserts that predation by sea urchins poses a threat
to bull kelp. The petitioner identifies trophic imbalances associated
with the loss of urchin predators, such as the sea otter and sunflower
sea star, as a factor that can devastate the bull kelp ecosystem and
lead to the development of urchin barrens. Urchin barrens may form when
urchin herbivory results in kelp deforestation and a community
dominated by crustose coralline algae. They assert that urchin barrens
have occurred along the North American west coast, from north of San
Francisco to the Oregon border. Although urchin predation has been
attributed as one of the primary stressors to kelp in Mendocino and
Sonoma counties in Northern California, Hamilton et al. (2020)
demonstrated that Oregon bull kelp population sizes were not
significantly affected by the increase in urchin density that occurred
in connection with the 2014 marine heat wave. Bull kelp have persisted
in Oregon despite the functional extinction of sea otters and recent
decline in sunflower sea stars (Hamilton et al. 2020). Similarly,
Tolmieri et al. (2023) did not observe a strong, negative correlation
between urchins and canopy kelp species in Washington.
The petitioner asserts that urchin barrens may become alternate
stable-states of the ecosystem in which a return to a kelp forest state
would be difficult. Although the development of alternate stable-states
may occur, there is significant spatiotemporal variation in the
ecological processes that sustain such states. For example, pathogen
induced sea urchin mortality has resulted in repeated flipping between
kelp forests and urchin barrens in Nova Scotia. Pathogen-induced sea
urchin mortality has also been observed in California (Steneck and
Johnson, 2013). In addition, urchin biomass removal due to a directed
fishery or as a kelp restoration action may shift barrens back to kelp
forest communities (Steneck and Johnson, 2013, Williams et al. 2021,
Eger et al. 2022).
The petitioner also claims that sea urchin predation will be
worsened by climate change due to reductions in kelp density associated
with increased and stronger storm systems. They claim that a decrease
in kelp density would increase predation from sea urchins. Although
strong storm events have the potential to reduce the size of kelp
forests, bull kelp has been observed to rapidly recolonize disturbed
areas following removal of more competitively dominant algal species
(Springer et al., 2010). Thus, in some cases, storm energy may have a
positive effect on bull kelp abundance. In contrast to the above
assertion, Dayton et al. (1992) noted an increase in urchin predation
in response to the loss of drift kelp, not a decrease in kelp density.
The petition presents credible information that predation by sea
urchins has created barrens in some areas. However, the long-term data
readily available in our files suggest that bull kelp is actually
increasing or stable within regions that encompass those smaller areas
that have been impacted by localized urchin predation. Therefore, we
conclude that the petition does not present substantial information
indicating that disease or predation is posing a threat to bull kelp
such that it is contributing to extinction risk.
Inadequacy of Existing Regulatory Mechanisms
The petitioner asserts the existing regulatory mechanisms are
insufficient to protect bull kelp from extinction and that bull kelp
does not currently hold protected status under any environmental law.
The only regulatory mechanism identified by the petitioner is that
provided by the National Marine Sanctuary System, and they assert that
such protections are only provided in the southernmost part of the bull
kelp habitat range. The petitioner incorrectly asserts that there are
no National Marine Sanctuaries in Washington. To the contrary, the
Olympic Coast National Marine Sanctuary includes 3,188 square miles of
marine water including the nearshore waters off the Olympic Peninsula
in the State of Washington. The petitioner does not specify particular
threats for which existing regulatory mechanisms are inadequate and
does not provide substantial scientific or commercial information to
support their assertion. Given this lack of specificity, we note below
some of the existing regulatory mechanisms that address manmade factors
identified elsewhere in the petition.
Although the petitioner asserts that bull kelp does not currently
hold protected status under any environmental law, they note elsewhere
in the petition that the California Fish and Game Commission approved a
3-year temporary closure of bull kelp commercial harvest off Sonoma and
Mendocino counties in California, and limited harvest off Humboldt and
Del Norte counties. This is a regulatory mechanism designed to protect
against an overutilization threat. We also note that the State of
California has initiated the development of a statewide, climate-ready
Kelp Restoration and Management Plan for California, which will include
a harvest management framework and other fishery management plan
elements required by the State of California's Marine Life Management
Act, an innovative framework for ecosystem-based management of kelp
forests, and a restoration toolkit consisting of restoration options
available to resource managers in California. In addition, as described
previously in Overutilization for commercial, recreational, scientific
or educational purposes, there are management frameworks for bull kelp
in place throughout its range that regulate the harvest and/or use of
bull kelp for any purpose.
The U.S. Army Corps of Engineers South Pacific Division also
considers kelp to be a special aquatic site (40 CFR 230 Section
404(b)(1) Guidelines). This status provides special consideration when
evaluating permit applications for dredged or fill material pursuant to
Section 404 of the Clean Water Act. This is a regulatory mechanism that
can address aspects of the coastal darkening factor identified in Other
natural or manmade factors affecting the bull kelp's continued
existence section of the petition. In addition, canopy kelp, which
includes bull kelp, has been designated as essential fish habitat (EFH)
pursuant to the Magnuson-Stevens Fishery Conservation and Management
Act for various federally managed fish species under the Pacific Coast
Groundfish (PCG) and Pacific Coast Salmon (PCS) Fishery Management
Plans (FMPs). Moreover, canopy kelp has been designated as a habitat
area of particular concern (HAPC) for various fish species under the
PCG and PCS FMPs. Federal agencies must consult with NMFS regarding any
proposed action that may adversely affect EFH or a HAPC, and must
consider NMFS's conservation recommendations to mitigate any
environmental impacts to bull kelp
[[Page 40789]]
during construction and other development.
We conclude that the information presented in the petition and
readily available to us does not constitute substantial information
indicating that the inadequacies of existing regulatory mechanisms are
posing a threat to bull kelp. To the contrary, information readily
available to us indicates a number of existing regulatory mechanisms
which assist in kelp protection.
Other Natural or Manmade Factors
The petitioner asserts that chemical pollution, thermal pollution,
coastal darkening, and oil spills pose risks to bull kelp and place the
species at risk of extinction. For example, the petitioner expresses
concern that thermal pollution created by power plants can jeopardize
reproduction of bull kelp. Though there are a few coastal power plants
that continue to discharge warm water, California has established
regulations that are phasing out once-through cooling water for energy
production. In addition, the Diablo Canyon power plant in central
California is currently scheduled for decommissioning and is not
anticipated to continue discharging warm water over the long term. San
Onofre Nuclear Generating Station (SONGS) was the only other coastal
power plant in California that discharged warm water in the vicinity of
kelp habitat, but it is currently being decommissioned. Moreover, the
California Coastal Commission required SONGS to provide compensatory
mitigation for the adverse effects to kelp and the marine environment
resulting in the largest artificial reef project on the West Coast of
the United States. As such, it seems that the threat of thermal
pollution by power plants has diminished substantially and there is no
indication of that pattern reversing in the foreseeable future.
Similar to thermal pollution, the petitioner claims chemical
pollution can inhibit kelp reproduction, settlement, and survival,
citing evidence from California and for other kelp species in South
America. The petition specifically cites concerns around the impacts of
hydrazine and heavy metals on bull kelp, pollutants emerging from
coastal factories, military bases, and airports. However, the petition
did not provide substantial scientific or commercial information to
support these assertions, such as documentation of existing overlap
between sources of these chemical pollutants and bull kelp populations
and associated negative impacts.
Coastal darkening, defined by the petitioner as a situation that
arises when pollutants from coastal runoff physically block the sun, is
claimed as a stressor inhibiting bull kelp photosynthesis, and thereby
growth and maturation, as well as bull kelp recruitment. The evidence
that coastal darkening affects photosynthesis cited by the petitioner
is focused on a different species of kelp, although the petitioner does
provide support for the negative impacts of turbidity on photosynthesis
and recruitment in bull kelp specifically. Importantly, though, the
petition does not present evidence that human activities causing
coastal darkening within the range of bull kelp reduce photosynthesis
and recruitment of bull kelp.
Finally, the petitioner presents evidence from laboratory studies
and asserts that oil spills, which can expose bull kelp to petroleum
and polycyclic aromatic hydrocarbons (PAHs) in particular, threaten
growth and photosynthesis, thereby increasing extinction risk. This
concern is specific to California and Alaska bull kelp habitats where
oil and gas development occurs. While some studies have demonstrated
negative effects of petroleum products on bull kelp, Springer et al.
(2010) indicate that little is known about the effects of toxicants
such as oil on bull kelp. For example, studies focused on the Exxon
Valdez oil spill in Alaska compared bull kelp biomass and percent cover
between oiled and control sites in Prince William Sound and found no
evidence of detrimental effects of oil exposure (Springer et al. 2010).
While oil spills are a threat to coastal ecosystems, the petition fails
to present credible scientific or commercial information indicating
that these forms of pollution are posing a threat to bull kelp.
Petition Finding
In conclusion, after reviewing the petition, the literature cited
in the petition, and other information readily available in our files,
we do not find there is substantial information indicating that bull
kelp is declining throughout all or a significant portion of its range
or that it is affected by threats throughout all or a significant
portion of its range such that listing may be warranted. We therefore
conclude the petition does not present substantial scientific or
commercial information indicating that the petitioned action to list N.
luetkeana as a threatened or endangered species may be warranted.
References Cited
A complete list of all references cited herein is available upon
request (See FOR FURTHER INFORMATION CONTACT).
Authority: The authority for this action is the Endangered Species
Act of 1973, as amended (16 U.S.C. 1531 et seq.).
Dated: June 14, 2023.
Samuel D. Rauch, III,
Deputy Assistant Administrator for Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. 2023-13277 Filed 6-21-23; 8:45 am]
BILLING CODE 3510-22-P