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1. Pseudo-nitzschia Bloom Dynamics in the Gulf of Maine: 2012–2016

   Clark, Suzanna; Hubbard, Katherine A.; Anderson, Donald M.; McGillicuddy Jr., Dennis J.; Ralston, David K.; Townsend, David W. (September 2019, Harmful algae)

   The toxic diatom genus Pseudo-nitzschia is a growing presence in the Gulf of Maine (GOM), where regionally unprecedented levels of domoic acid (DA) in 2016 led to the first Amnesic Shellfish Poisoning closures in the region. However, factors driving GOM Pseudo-nitzschia dynamics, DA concentrations, and the 2016 event are unclear. Water samples were collected at the surface and at depth in offshore transects in summer 2012, 2014, and 2015, and fall 2016, and a weekly time series of surface water samples was collected in 2013. Temperature and salinity data were obtained from NERACOOS buoys and measurements during sample collection. Samples were processed for particulate DA (pDA), dissolved nutrients (nitrate, ammonium, silicic acid, and phosphate), and cellular abundance. Species composition was estimated via Automated Ribosomal Intergenic Spacer Analysis (ARISA), a semi-quantitative DNA finger-printing tool. Pseudo-nitzschia biogeography was consistent in the years 2012, 2014, and 2015, with greater Pseudo-nitzschia cell abundance and P. plurisecta dominance in low-salinity inshore samples, and lower Pseudo-nitzschia cell abundance and P. delicatissima and P. seriata dominance in high-salinity offshore samples. During the 2016 event, pDA concentrations were an order of magnitude higher than in previous years, and inshore-offshore contrasts in biogeography were weak, with P. australis present in every sample. Patterns in temporal and spatial variability confirm that pDA increases with the abundance and the cellular DA of Pseudo-nitzschia species, but was not correlated with any one environmental factor. The greater pDA in 2016 was caused by P. australis – the observation of which is unprecedented in the region – and may have been exacerbated by low residual silicic acid. The novel presence of P. australis may be due to local growth conditions, the introduction of a population with an anomalous water mass, or both factors. A definitive cause of the 2016 bloom remains unknown, and continued DA monitoring in the GOM is warranted. 

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2. A Time Series of Water Column Distributions and Sinking Particle Flux of Pseudo-Nitzschia and Domoic Acid in the Santa Barbara Basin, California

   https://doi.org/10.3390/toxins10110480  

   Umhau, Blaire; Benitez-Nelson, Claudia; Anderson, Clarissa; McCabe, Kelly; Burrell, Christopher (November 2018, Toxins)

   Water column bulk Pseudo-nitzschia abundance and the dissolved and particulate domoic acid (DA) concentrations were measured in the Santa Barbara Basin (SBB), California from 2009–2013 and compared to bulk Pseudo-nitzschia cell abundance and DA concentrations and fluxes in sediment traps moored at 147 m and 509 m. Pseudo-nitzschia abundance throughout the study period was spatially and temporally heterogeneous (<200 cells L−1 to 3.8 × 106 cells L−1, avg. 2 × 105 ± 5 × 105 cells L−1) and did not correspond with upwelling conditions or the total DA (tDA) concentration, which was also spatially and temporally diverse (<1.3 ng L−1 to 2.2 × 105 ng L−1, avg. 7.8 × 103 ± 2.2 × 104 ng L−1). We hypothesize that the toxicity is likely driven in part by specific Pseudo-nitzschia species as well as bloom stage. Dissolved (dDA) and particulate (pDA) DA were significantly and positively correlated (p < 0.01) and both comprised major components of the total DA pool (pDA = 57 ± 35%, and dDA = 42 ± 35%) with substantial water column concentrations (>1000 cells L−1 and tDA = 200 ng L−1) measured as deep as 150 m. Our results highlight that dDA should not be ignored when examining bloom toxicity. Although water column abundance and pDA concentrations were poorly correlated with sediment trap Pseudo-nitzschia abundance and fluxes, DA toxicity is likely associated with senescent blooms that rapidly sink to the seafloor, adding another potential source of DA to benthic organisms. 

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3. Basin‐Wide Shift in Bowhead Whale Migration in the Pacific Arctic

   https://doi.org/10.1029/2023GL106416  

   Szesciorka, Angela_R; Stafford, Kathleen_M; Berchok, Catherine_L (February 2024, Geophysical Research Letters)

   Abstract In a rapidly changing Arctic, multiple lines of evidence suggest that bowhead whale migration is changing. To explore these changes further, we used passive acoustic data to examine bowhead whale presence in the western Beaufort Sea (12 years) and Chukchi Plateau (11 years) spanning 2008 to 2022. Departure from the western Beaufort Sea shifted 45 days later over the 12‐year period. Summer presence increased at both sites, suggesting feeding areas within the Chukchi Sea are becoming more favorable. Likewise, findings from the Bering Strait suggest that some whales are remaining north of the Bering Strait for the winter instead of in the Bering Sea. These Pacific Arctic‐wide changes to migration have occurred over only one decade. Questions remain about prey availability in the Chukchi Sea, implications of migratory changes, such as a northward shift in the core overwintering area, and impact to communities south of the Bering Strait. 

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4. Sea ice directs changes in bowhead whale phenology through the Bering Strait

   https://doi.org/10.1186/s40462-023-00374-5  

   Szesciorka, Angela_R; Stafford, Kathleen_M (February 2023, Movement Ecology)

   Abstract BackgroundClimate change is warming the Arctic faster than the rest of the planet. Shifts in whale migration timing have been linked to climate change in temperate and sub-Arctic regions, and evidence suggests Bering–Chukchi–Beaufort (BCB) bowhead whales (Balaena mysticetus) might be overwintering in the Canadian Beaufort Sea. MethodsWe used an 11-year timeseries (spanning 2009–2021) of BCB bowhead whale presence in the southern Chukchi Sea (inferred from passive acoustic monitoring) to explore relationships between migration timing and sea ice in the Chukchi and Bering Seas. ResultsFall southward migration into the Bering Strait was delayed in years with less mean October Chukchi Sea ice area and earlier in years with greater sea ice area (p = 0.04, r² = 0.40). Greater mean October–December Bering Sea ice area resulted in longer absences between whales migrating south in the fall and north in the spring (p < 0.01, r² = 0.85). A stepwise shift after 2012–2013 shows some whales are remaining in southern Chukchi Sea rather than moving through the Bering Strait and into the northwestern Bering Sea for the winter. Spring northward migration into the southern Chukchi Sea was earlier in years with less mean January–March Chukchi Sea ice area and delayed in years with greater sea ice area (p < 0.01, r² = 0.82). ConclusionsAs sea ice continues to decline, northward spring-time migration could shift earlier or more bowhead whales may overwinter at summer feeding grounds. Changes to bowhead whale migration could increase the overlap with ships and impact Indigenous communities that rely on bowhead whales for nutritional and cultural subsistence. 

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5. Changes in the oxygen isotope composition of the Bering Sea contribution to the Arctic Ocean are an independent measure of increasing freshwater fluxes through the Bering Strait

   https://doi.org/10.1371/journal.pone.0273065  

   Cooper, Lee W.; Magen, Cédric; Grebmeier, Jacqueline M. (August 2022, PLOS ONE)

   Doi, Hideyuki (Ed.)

   A large volume of freshwater is incorporated in the relatively fresh (salinity ~32–33) Pacific Ocean waters that are transported north through the Bering Strait relative to deep Atlantic salinity in the Arctic Ocean (salinity ~34.8). These freshened waters help maintain the halocline that separates cold Arctic surface waters from warmer Arctic Ocean waters at depth. The stable oxygen isotope composition of the Bering Sea contribution to the upper Arctic Ocean halocline was established as early as the late 1980’s as having a δ 18 O V - SMOW value of approximately -1.1‰. More recent data indicates a shift to an isotopic composition that is more depleted in 18 O (mean δ 18 O value ~-1.5‰). This shift is supported by a data synthesis of >1400 water samples (salinity from 32.5 to 33.5) from the northern Bering and Chukchi seas, from the years 1987–2020, which show significant year-to-year, seasonal and regional variability. This change in the oxygen isotope composition of water in the upper halocline is consistent with observations of added freshwater in the Canada Basin, and mooring-based estimates of increased freshwater inflows through Bering Strait. Here, we use this isotopic time-series as an independent means of estimating freshwater flux changes through the Bering Strait. We employed a simple end-member mixing model that requires that the volume of freshwater (including runoff and other meteoric water, but not sea ice melt) flowing through Bering Strait has increased by ~40% over the past two decades to account for a change in the isotopic composition of the 33.1 salinity water from a δ 18 O value of approximately -1.1‰ to a mean of -1.5‰. This freshwater flux change is comparable with independent published measurements made from mooring arrays in the Bering Strait (freshwater fluxes rising from 2000–2500 km 3 in 2001 to 3000–3500 km 3 in 2011). 

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