Marine mammal visual and acoustic surveys near the Alaskan Colville River Delta

Information about the occurrence of marine mammals near the Colville River Delta (CRD), Beaufort Sea, Alaska is limited for most species expected to occur in this region. As part of marine mammal monitoring and mitigation for a seismic acquisition program August 25-September 30, 2014, we recorded marine mammal occurrence in a 30km(2) survey area between the Spy Islands and Oliktok Point near Simpson Lagoon using a combination of visual and acoustic monitoring methods. Visual effort totaled 632h, occurring 18-20h/day during all daylight hours by observers aboard three small survey vessels. In addition, an Inupiat observer and seal hunter from the village of Nuiqsut conducted a small-vessel survey to investigate locations of Phoca largha haul-out sites. A total of 102 individual marine mammals were recorded from five species: P. largha, Pusa hispida, Ursus maritimus, Erignathus barbatus, and Delphinapterus leucas. Over 400h of acoustic data were recorded using second-generation Ecological Acoustic Recorders deployed on the seafloor at three locations. Calls were identified for D. leucas, Balaena mysticetus, E. barbatus, and P. hispida. Results provide valuable information on marine mammal occurrence for the Beaufort Sea CRD during summer/fall, an area proposed for potential offshore oil and gas development

Preparing for The Inevitable: Ecological and Indigenous Community Impacts of Oil Spill-Related Mortality in The United States’ Arctic Marine Ecosystem

While hydrocarbon exploration and extraction in the Arctic ebb and flow, reduced sea ice has opened new travel routes across the Arctic. The opening of the Northwest Passage has allowed larger ships (including oil tankers) and higher traffic into remote regions. More ice loss is expected in the future. With this comes the potential for hydrocarbon spills. To quantify the ecosystem impacts of a spill in the Alaska North Slope region, an Ecospace model using the Ecopath with Ecosim software was developed. We highlight the impacts of four potential hydrocarbon contamination scenarios: a subsurface crude oil pipeline release, a surface platform oil spill, a surface cruise ship diesel spill, and a surface tanker oil spill. Hydrocarbon contamination was modeled using SIMAP (Spill Impact Model Analysis Package), which was developed from the oil fate sub-model in the Natural Resource Damage Assessment Model for the US Department of the Interior and under the Comprehensive Environmental Response, Compensation and Liability Act of 1980 (CERCLA). Spatial-temporal SIMAP results were coupled to the Ecospace model. We show that in all four hydrocarbon contamination scenarios, there are spatial changes in harvested species resulting in long-term declines in harvest levels for the communities within the model area (Nuiqsut, Kaktovik, and Barrow Alaska), depending on the severity of the scenario. Responses to hydrocarbon events are likely to be slow in the Arctic, limited by the ice-free season. We highlight this area for scenario testing as ecological impacts are also an issue of food security to the local communities and human health issue

Data from: Mitogenomic phylogenetics of fin whales (Balaenoptera physalus spp.): genetic evidence for revision of subspecies

There are three described subspecies of fin whales (Balaenoptera physalus): B. p. physalus Linnaeus, 1758 in the Northern Hemisphere, B. p. quoyi Fischer, 1829 in the Southern Hemisphere, and a recently described pygmy form, B. p. patachonica Burmeister, 1865. The discrete distribution in the North Pacific and North Atlantic raises the question of whether a single Northern Hemisphere subspecies is valid. We assess phylogenetic patterns using ~16 K base pairs of the complete mitogenome for 154 fin whales from the North Pacific, North Atlantic - including the Mediterranean Sea - and Southern Hemisphere. A Bayesian tree of the resulting 136 haplotypes revealed several well-supported clades representing each ocean basin, with no haplotypes shared among ocean basins. The North Atlantic haplotypes (n = 12) form a sister clade to those from the Southern Hemisphere (n = 42). The estimated time to most recent common ancestor (TMRCA) for this Atlantic/Southern Hemisphere clade and 81 of the 97 samples from the North Pacific was approximately 2 Ma. 14 of the remaining North Pacific samples formed a well-supported clade within the Southern Hemisphere. The TMRCA for this node suggests that at least one female from the Southern Hemisphere immigrated to the North Pacific approximately 0.37 Ma. These results provide strong evidence that North Pacific and North Atlantic fin whales should not be considered the same subspecies, and suggest the need for revision of the global taxonomy of the species. There were a total of 103 CR haplotypes in the Sanger-sequenced data set (Table 1). Haplotypic diversity was high both within ocean basins as well as across all samples. The minimum diversity within an ocean basin was 0.828 for the North Atlantic, which also had the fewest samples. There were no shared haplotypes among ocean basins. There were two fixed differences between the North Atlantic and North Pacific (sites 181 and 198), and one between the North Atlantic and Southern Hemisphere sequences (site 198)