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Ben Weitzman

Publications and source records attributed to Ben Weitzman.

11 recordsLinked to original sources

Quantifying sea otter abundance, distribution, habitat use, and foraging intake in Cook Inlet, Alaska

Following near extirpation from the fur trade, sea otters ( Enhydra lutris ) have returned to occupy lower Cook Inlet since the 1950s, or earlier, with numbers increasing to ~11,000 and ~9,000 on the west and east side, respectively, by 2017. Northward range expansion on the west side has been negligible for decades with few animals found north of Kamishak Bay, while northward expansion on the east side has been more pronounced in recent decades. The reasons for these contrasting distribution patterns are not certain. Possible explanations for lack of expansion on the west side included 1) poor sea otter habitat north of Kamishak Bay; 2) adequate habitat north of Kamishak Bay but no incentive for sea otters to move north because of abundant food in Kamishak Bay, and/or sea otters discouraged from moving north of Kamishak Bay; 3) seasonal ice formation; or 4) seasonal presence of killer whales. This project was designed to document current sea otter abundance and distribution in lower Cook Inlet, including seasonal variation, and evaluate drivers of habitat use and foraging conditions, including how these overlap with Bureau of Ocean Energy Management (BOEM) Lease Sale blocks. We found that the probability of sea otter presence in lower Cook Inlet was significantly related to depth and distance from shore with the highest probabilities of sea otter presence in areas ~7–8 kilometers (km) from shore in water ~20–30 meters (m) deep. Historical survey data suggest sea otter distribution has not changed dramatically since 2002, and while we detected significant seasonal changes including due to presence of heavy sea ice, the seasonal changes were modest and primarily related to locations with consistent winter ice formation on the west side of lower Cook Inlet. Overall, throughout the year, sea otters appeared to be utilizing most of the habitat within the 40-m depth contour on the east side of lower Cook Inlet, including Kachemak Bay. Sea otters on the west side reside largely within Kamishak Bay. Because of the shallow bathymetry of lower Cook Inlet, sea otters consistently occurred farther offshore than in many other areas of Alaska. The presence of sea otters, including females with pups, in these offshore waters indicates that sea otters can forage productively in these open water areas. Importantly, we documented that sea otters, including females with pups, occurred in most of the eastern BOEM lease blocks including the original Lease Sale 244 blocks 7064, 7114, 6162, 6310, 6360, 6410, 6458 and 6457. The relinquishments for these 7 leases were effective September 17, 2024: OCS-Y-02434 (block # 7064), OCS-Y-02435 (7114), OCS-Y-02436 (6162), OCS-Y-02438 (6357), OCS-Y-02442 (6407), OCS-Y02446 (6457), OCS-Y-02447 (6458) https://www.boem.gov/sites/default/files/documents/environment/Map%20of%20Active%20Leases%20 Cook%20Inlet%20OCS_0.pdf Regarding differential northward expansion on the east and west side of lower Cook Inlet, we found that wind and water circulation patterns make winter sea ice more prominent on the west side, but this had minimal effects on sea otter distribution. In addition, although there have been observations of killer whale ( Orcinus orca ) predation on sea otters in Cook Inlet, we did not see behavioral or distributional evidence that it was prevalent enough to have strong effects on sea otter habitat use. Benthic surveys using a remotely operated vehicle (ROV) indicated that epibenthic substrate and biological community heterogeneity differed between areas with and without otters, suggesting that these factors may explain the current distribution of otters within lower Cook Inlet. However, ROV surveys cannot assess infaunal prey abundance, making assessments of the role of prey availability difficult. The existence of a healthy Pacific razor clam ( Siliqua patula ) fishery along western lower Cook Inlet along the Lake Clark coast north of Kamishak Bay suggests there may still be a resource base for eventual expansion of sea otters into this area. Our shore-based forage observations indicated that sea otters exist near carrying capacity densities relative to nearshore prey resources. However, our distribution model suggests the bulk of the population lives offshore beyond our ability to observe their feeding activity. The fact that sea otters are a consistent presence in offshore areas suggests that prey resources in these areas were relatively abundant in comparison to nearshore prey resources, making foraging in offshore areas, with water depths of 0–40 m, energetically profitable. Prey types in these offshore areas of lower Cook Inlet likely included epifauna such as crabs and large urchins, in addition to infaunal clams based on the soft substrate habitat types that characterize lower Cook Inlet. Collectively, our results suggest that sea otters occupy most areas of lower Cook Inlet with appropriate benthic habitat types and prey resources, which includes areas within BOEM Lease Sale blocks. With the exception of the Lake Clark coast, sea otters may be approaching a food- and habitat-limited distribution and carrying capacity, suggesting that the current status of sea otters in lower Cook Inlet is likely to remain similar in the absence of significant changes to prey, habitat, predation, or anthropogenic disturbance.

Alaska

The dynamics of sea otter prey selection under population growth and expansion

Sea otters ( Enhydra lutris ) were extirpated from much of their range in the North Pacific by the early 1900s but have made a remarkable recovery in Southeast Alaska. Sea otter populations have been particularly successful in Glacier Bay, Alaska, a protected tidewater glacier fjord with a diverse and productive nearshore habitat. Collection of sea otter foraging observations in Glacier Bay began in 1993, along with high-resolution aerial surveys that provide estimates of sea otter abundance and distribution. We integrated these two data sources to investigate how sea otter diet changed in space and time as sea otters established and spread across Glacier Bay. Specifically, we developed a multilevel Bayesian model to capture how sea otter diet at a location (the number, type, and size of prey collected) changed as a function of local cumulative otter abundance and the year in which the location was first occupied. This framework enabled us to estimate the sequence of sea otter prey selection and switching as prey populations responded to sea otter foraging pressure. We found that local sea otter diet changed substantially as the population established, shifting away from large urchins, crabs, and clams to Modiolus mussels and small urchins, and lastly to small clams and Mytilus mussels. We also found that sea otter diet at newly occupied sites changed as otters spread over the main channel and into the arms of Glacier Bay. Further, by 2019, sea otters across the bay were primarily foraging on small prey, regardless of the local occupancy history. The absence of a spatial gradient in the size of prey captured late in the study suggests that feedbacks between the top-down effects of sea otter foraging, sea otter dispersal processes, and local variation in habitat productivity may have homogenized the size structure of available prey across Glacier Bay.

Alaska

Nearshore ecosystems in the Gulf of Alaska

Nearshore ecosystem monitoring in western Prince William Sound, Kenai Fjords National Park, Kachemak Bay, and Katmai National Park and Preserve has been conducted as a single Nearshore Component of the Gulf Watch Alaska program over the past five years (2017-2021). This program builds on the previous five years and continues, in many cases, decades of preceding research and monitoring. During the 2017-2021 period of Gulf Watch Alaska, we successfully collected data on more than 200 nearshore metrics across all regions. These metrics were explicitly selected because of their value as trophically-connected features that offer insights into causes of changes through bottom-up and top-down forces within the nearshore food web. During these past 5 years, this study design has been applied to documenting and understanding several perturbations, including the Pacific Marine Heatwave and loss of sea stars due to sea star wasting. Continued monitoring will allow for a better understanding of change in nearshore ecosystems across the Gulf of Alaska and the status of spill injured resources, including greater perspective on oil spill effects and recovery relative to other types of perturbations. This information will be critical for anticipating and responding to ongoing and future changes in the region, as well as providing data for understanding global-scale variation in marine environments.

Alaska

Divergent gene expression profiles in Alaskan sea otters: An indicator of chronic domoic acid exposure?

An opportunistic investigation into ecosystem instability in Kachemak Bay (KBay), Alaska, has led us to investigate exposure to toxic algae in sea otters. We used gene expression to explore the physiological health of sea otters sampled in KBay in May 2019. We found altered levels of gene transcripts in comparison with reference sea otters from clinically normal, oil-exposed, and nutritionally challenged populations sampled over the past decade. KBay sea otters were markedly divergent from the other groups for five genes, which indicated the involvement of neurological, cardiac, immune, and detoxification systems. Further, analyses of urine and fecal samples detected domoic acid in the KBay sea otters. In combination, these results may point to chronic, low-level exposure to an algal toxin, such as domoic acid. With a warming climate, the frequency and severity of harmful algal blooms in marine environments is anticipated to increase, and novel molecular technologies to detect sublethal or chronic exposure to algal toxins will help provide an early warning of threats to the stability of populations and ecosystems.

Alaska

Evidence of increased mussel abundance related to the Pacific marine heatwave and sea star wasting

Mussels occupy a key middle trophic position in nearshore food webs linking primary producers to predators. Climate-related environmental changes may synergistically combine with changes in predator abundance to affect intertidal ecosystems. We examined the influence of two major events on mussel ( Mytilus trossulus ) abundance in the northern Gulf of Alaska: the recent Pacific marine heatwave (PMH, 2014–2016) and an outbreak of sea star wasting (SSW). We investigated how mussel abundance changed since the onset of SSW and whether the density of predatory sea stars or PMH-related temperature metrics explain variation in mussel abundance. Sea stars and mussels were surveyed since 2005 approximately annually in four regions of the northern Gulf of Alaska: Katmai (KATM), Kachemak Bay (KBAY), Kenai Fjords (KEFJ) and western Prince William Sound (WPWS). Mussel percent cover in the mid-intertidal increased 1–3 years after declines in sea stars at all regions and in the low-intertidal at KATM, KBAY, and KEFJ, but not at WPWS. After the onset of SSW, large (≥20 mm length) mussel density and mussel bed width increased at KATM but not the other regions. Total mussel densities, including recruits, did not differ before and after the onset of SSW. The total number of sea stars significantly explained variation in mussel metrics, but the proportions of the three sea star species examined did not. We did not find strong evidence for direct effects of temperature on mussels. The effects of the PMH and the SSW outbreak appear to have combined, with increased temperatures indirectly benefiting mussels in concert with relaxed top-down pressure from sea stars, allowing for increased mussel abundance. Changing mussel abundance may affect intertidal local productivity and the abundance or performance of other nearshore consumers of mussels.

Alaska

Sea otter population collapse in southwest Alaska: Assessing ecological covariates, consequences, and causal factors

Sea otter ( Enhydra lutris ) populations in southwest Alaska declined substantially between about 1990 and the most recent set of surveys in 2015. Here we report changes in the distribution and abundance of sea otters, and covarying patterns in reproduction, mortality, body size and condition, diet and foraging behavior, food availability, health profiles, and exposure to environmental contaminants over this 25-yr period. The population decline, which resulted in densities on the order of 5% of environmental carrying capacity, ranged from Attu Island in the west to about Castle Cape (on the south side of the Alaska Peninsula) in the east. Remaining sea otters moved closer to shore and into shallow, protected habitats. Reproductive rates appeared unchanged with the decline. Although the demographic cause of the decline was clearly elevated mortality, stranded carcasses were rare or absent. The net rate of energy gain by foraging sea otters, body length and condition, and prey biomass density, all increased after the decline and varied inversely with sea otter population density beyond the area of decline. Sea otters within the area of decline showed no increases in health anomalies, disease, contaminant exposure, or abnormal gene transcription patterns as compared to animals outside the area of decline. These collective findings are inconsistent with nutritional limitation, disease, or environmental contaminants, and consistent with predation (or possibly some other density-independent factor) as the reason for the sea otter population decline. Our approach and analyses provide a broad conceptual template for thinking about and assessing the causes of wildlife population declines.

Alaska

Changes in rocky intertidal community structure during a marine heatwave in the northern Gulf of Alaska

Marine heatwaves are global phenomena that can have major impacts on the structure and function of coastal ecosystems. By mid-2014, the Pacific Marine Heatwave (PMH) was evident in intertidal waters of the northern Gulf of Alaska and persisted for multiple years. While offshore marine ecosystems are known to respond to these warmer waters, the response of rocky intertidal ecosystems to this warming is unclear. Intertidal communities link terrestrial and marine ecosystems and their resources are important to marine and terrestrial predators and to human communities for food and recreation, while simultaneously supporting a growing coastal tourism industry. Given that current climate change projections suggest increased frequency and duration of marine heatwaves, monitoring and understanding the impacts of heatwaves on intertidal habitats is important. As part of the Gulf Watch Alaska Long-Term Monitoring program, we examined rocky intertidal community structure at 21 sites across four regions spanning 1,200 km of coastline: Western Prince William Sound, Kenai Fjords National Park, Kachemak Bay, and Katmai National Park and Preserve. Sites were monitored annually from 2012 to 2019 at mid and low tidal strata. Before-PMH (2012–2014), community structure differed among regions. We found macroalgal foundation species declined during this period mirroring patterns observed elsewhere for subtidal habitat formers during heatwave events. The region-wide shift from an autotroph-macroalgal dominated rocky intertidal to a heterotroph-filter-feeder dominated state concurrent with the changing environmental conditions associated with a marine heatwave event suggests the PMH had Gulf-wide impacts to the structure of rocky intertidal communities. During/after-PMH (2015–2019), similarities in community structure increased across regions, leading to a greater homogenization of these communities, due to declines in macroalgal cover, driven mostly by a decline in the rockweed, Fucus distichus , and other fleshy red algae in 2015, followed by an increase in barnacle cover in 2016, and an increase in mussel cover in 2017. Strong, large-scale oceanographic events, like the PMH, may override local drivers to similarly influence patterns of intertidal community structure.

Alaska

Biological correlates of sea urchin recruitment in kelp forest and urchin barren habitats

Shifts between the alternate stable states of sea urchin barren grounds and kelp forests correspond to sea urchin density. In the Aleutian Archipelago, green sea urchins Strongylocentrotus polyacanthus are the dominant herbivores that graze kelp forests. Sea urchin recruitment is an important driver that influences sea urchin density, particularly in the absence of top-down control from a keystone predator such as the sea otter Enhydra lutris . To understand how the biological community may influence patterns of sea urchin recruitment, we compared sea urchin recruit (size ≤20 mm) densities with biomass of other benthic organisms in both barren ground and kelp forest habitats at 9 islands across the Aleutian Archipelago. Patterns of biological community structure between the 2 habitats did not explain patterns of sea urchin recruits; however, the same 10 specific taxa were found to correlate with sea urchin recruits in each habitat. Taxa that showed strong positive correlations included Codium, Constantinea, Schizymenia, and hydrozoans, while strong negative correlations were observed with Pachyarthron and Pugettia . Weak positive correlations were observed with Alcyonidium and ascidiaceans in both habitats, while weak variable relationships were detected with Polysiphonia and Corallina between habitats. The observed species-specific relationships may be due to small sea urchin displacement by larger conspecifics, larval responses to settlement cues, post-settlement survival via biogenic refugia, or potentially predation. These potential species-specific interactions were apparent, regardless of habitat, and it can be inferred that they would be preserved in the presence or absence of keystone predation.

Alaska

Keystone predators govern the pathway and pace of climate impacts in a subarctic marine ecosystem

Predator loss and climate change are hallmarks of the Anthropocene yet their interactive effects are largely unknown. Here, we show that massive calcareous reefs, built slowly by the alga Clathromorphum nereostratum over centuries to millennia, are now declining because of the emerging interplay between these two processes. Such reefs, the structural base of Aleutian kelp forests, are rapidly eroding because of overgrazing by herbivores. Historical reconstructions and experiments reveal that overgrazing was initiated by the loss of sea otters, Enhydra lutris (which gave rise to herbivores capable of causing bioerosion), and then accelerated with ocean warming and acidification (which increased per capita lethal grazing by 34 to 60% compared with preindustrial times). Thus, keystone predators can mediate the ways in which climate effects emerge in nature and the pace with which they alter ecosystems.

Science

Size, growth, and density data for shallow-water sea urchins from Mexico to the Aleutian Islands, Alaska, 1956–2016

Size, growth, and density have been studied for North American Pacific coast sea urchins Strongylocentrotus purpuratus , S. droebachiensis, S. polyacanthus , Mesocentrotus (Strongylocentrotus) franciscanus , Lytechinus pictus , Centrostephanus coronatus , and Arbacia stellata by various workers at diverse sites and for varying lengths of time from 1956 to present. Numerous peer-reviewed publications have used some of these data but some data have appeared only in graduate theses or the gray literature. There also are data that have never appeared outside original data sheets. Motivation for studies has included fisheries management and environmental monitoring of sewer and power plant outfalls as well as changes associated with disease epidemics. Studies also have focused on kelp restoration, community effects of sea otters, basic sea urchin biology, and monitoring. The data sets presented here are a historical record of size, density, and growth for a common group of marine invertebrates in intertidal and nearshore environments that can be used to test hypotheses concerning future changes associated with fisheries practices, shifts of predator distributions, climate and ecosystem changes, and ocean acidification along the Pacific Coast of North America and islands of the north Pacific.

Pacific Coast

Aerial surveys of sea otters (Enhydra lutris) in Lower Cook Inlet, Alaska, May, 2017

Portions of two stocks of northern sea otters (Enhydra lutris kenyoni) occur in Lower Cook Inlet (LCI), Alaska. Sea otters on the west side of LCI are considered part of the southwest Alaska stock; sea otters occupying eastern LCI are considered part of the southcentral Alaska stock. Information concerning the distributions and abundance of sea otters in LCI is needed to track the status and trends of these populations and address management concerns associated with oil and gas exploration and coastal development in the region. In May 2017, we conducted a series of replicate aerial surveys of sea otters across LCI following the methods of Bodkin and Udevitz (1999). Our abundance estimate for western LCI (southwest Alaska stock) was 10,737 (SE = 2,323) sea otters. Sea otters were not uniformly distributed across western LCI. The highest sea otter densities (up to 8 sea otter/km2) occurred within Kamishak Bay to the west and north of Augustine Island. Sea otter densities were relatively low north of Kamishak Bay. The total abundance estimate for eastern LCI (part of the southcentral Alaska stock) was 9,152 (SE = 1,020) sea otters. The highest densities of sea otters in eastern LCI were found along the north shore of Kachemak Bay and in Port Graham. We also found large numbers of sea otters along the eastern shore of LCI between Anchor Point and Clam Gulch. We recommend conducting a sea otter distribution survey in September, prior to the appearance of sea ice, and again during winter to examine potential seasonal shifts in sea otter distributions in LCI.

Alaska