An early Holocene Greenland whale from Melville Bugt, Greenland

Radiocarbon age determination of a Greenland whale (Balaena mysticetus) vertebra from Melville Bugt in northwestern Greenland yields an age of 9259-8989 cal yr BP. The margin of the Greenland Ice Sheet in Melville Bugt was situated behind its AD 1950-2000 position in the early Holocene, at a similar position to that being reached following rapid retreat in recent years. Such an early deglaciation of areas close to the Greenland Ice Sheet is unusual. This probably reflects the unique glaciological setting resulting from the narrow fringe of ice-free islands and peninsulas and offshore waters with deep areas that characterize this part of Greenland. The timing of Greenland Ice Sheet retreat to its present margin varies significantly around Greenland.     

Distribution,seasonality, lengths,and feeding behaviour of whale sharks (Rhincodon typus) observed in New Zealand waters

Data from 36 whale shark (Rhincodon typus Smith, 1828) sightings off north‐east North Island, New Zealand are summarised. Sightings were concentrated over the outer shelf and shelf break in areas influenced by the East Auckland Current at sea surface temperatures (SST) of 21–24°C. Sightings occurred from late spring to early autumn (November‐April) but were most frequent in midsummer (February) when upwelling along the north‐east shelf is weakest. The data indicate whale sharks occur off north‐east New Zealand most summers, including those when SST is colder than usual. A cluster of sightings and three observations of whale sharks feeding on schools of anchovy (Engraulis australis) near Whale Island, Bay of Plenty, suggest whale sharks may aggregate seasonally in this area. Estimated total lengths (TL) of 26 whale sharks ranged from 3.5 to 15 m, with 73% between 6 and 9 m TL.     

High gray whale relative abundances associated with an oceanographic front in the south-central Chukchi Sea

We describe gray whale (Eschrichtius robustus) distribution in the south-central Chukchi Sea in relation to environmental factors during two 5-day surveys in June and September of 2003. Whale counts per 10-min scan (an index of relative abundance) ranged from 0 to 41 in June and from 0 to 28 in September. CTD data showed an ocean front around 67.8°N with strong horizontal gradients in temperature, salinity, chlorophyll-a concentration and water-column stability. Highest whale abundance indices occurred in or near the front in both periods. Preliminary qualitative assessment of biological communities in the study area suggests that infaunal clams, echinoderms, euphausids, chaetognaths and Arctic cod were common, while ampeliscid amphipods, the previously abundant infauna (and likely prey) in the nearby Chirikov Basin feeding area, were not dominant. Euphausids may be a prey for gray whales in this area. We suggest that frontal systems may play an important role in eastern North Pacific gray whale foraging grounds. Further study is needed to fully describe the role of frontal systems in gray whale foraging grounds.     

The sequential megafaunal collapse hypothesis: Testing with existing data

Springer et al. [Springer, A.M., Estes, J.A., van Vliet, G.B., Williams, T.M., Doak, D.F., Danner, E.M., Forney, K.A., Pfister, B., 2003. Sequential megafaunal collapse in the North Pacific Ocean: an ongoing legacy of industrial whaling? Proceedings of the National Academy of Sciences 100 (21), 12,223–12,228] hypothesized that great whales were an important prey resource for killer whales, and that the removal of fin and sperm whales by commercial whaling in the region of the Bering Sea/Aleutian Islands (BSAI) in the late 1960s and 1970s led to cascading trophic interactions that caused the sequential decline of populations of harbor seal, northern fur seal, Steller sea lion and northern sea otter. This hypothesis, referred to as the Sequential Megafaunal Collapse (SMC), has stirred considerable interest because of its implication for ecosystem-based management. The SMC has the following assumptions: (1) fin whales and sperm whales were important as prey species in the Bering Sea; (2) the biomass of all large whale species (i.e., North Pacific right, fin, humpback, gray, sperm, minke and bowhead whales) was in decline in the Bering Sea in the 1960s and early 1970s; and (3) pinniped declines in the 1970s and 1980s were sequential. We concluded that the available data are not consistent with the first two assumptions of the SMC. Statistical tests of the timing of the declines do not support the assumption that pinniped declines were sequential. We propose two alternative hypotheses for the declines that are more consistent with the available data. While it is plausible, from energetic arguments, for predation by killer whales to have been an important factor in the declines of one or more of the three populations of pinnipeds and the sea otter population in the BSAI region over the last 30 years, we hypothesize that the declines in pinniped populations in the BSAI can best be understood by invoking a multiple factor hypothesis that includes both bottom–up forcing (as indicated by evidence of nutritional stress in the western Steller sea lion population) and top–down forcing (e.g., predation by killer whales, mortality incidental to commercial fishing, directed harvests). Our second hypothesis is a modification of the top–down forcing mechanism (i.e., killer whale predation on one or more of the pinniped populations and the sea otter population is mediated via the recovery of the eastern North Pacific population of the gray whale). We remain skeptical about the proposed link between commercial whaling on fin and sperm whales, which ended in the mid-1960s, and the observed decline of populations of northern fur seal, harbor seal, and Steller sea lion some 15 years later.     

Implications of Arctic industrial growth and strategies to mitigate future vessel and fishing gear impacts on bowhead whales

The objective of this paper was to investigate and illustrate how insights gained from experience managing human activities in order to protect North Atlantic right whales (Eubalaena glacialis) along the heavily industrialized east coast of North America might be applied in the Arctic, where bowhead whales (Balaena mysticetus) face some of the same risks as right whales. The reduced extent and thickness of sea ice and the resultant longer open-water season have major, complex implications for the Arctic marine ecosystem. Increased maritime ship traffic and commercial fishing in the Arctic are bound to affect bowheads and Native (indigenous) hunting communities who depend on whales for subsistence and cultural identity. Bowheads and right whales were greatly depleted by commercial whaling in the 19th and early 20th centuries. While the Western Arctic bowhead population has been recovering steadily in recent decades, North Atlantic right whales remain highly endangered because of persistent lethal and sublethal vessel strikes and frequent entanglement in commercial fishing gear. Entanglement can be transitory or persistent, with debilitation lasting for months before the animal finally succumbs. Vessel strike and fishing gear trauma has been documented in bowheads, but at a much lower rate than in right whales. Initiatives intended to mitigate the impacts of ship traffic on North Atlantic right whales have included speed limits and routing changes. Those meant to reduce the incidence and severity of entanglements include the modification of gear design and gear deployment practices. Management measures need to be considered in advance in the Arctic in order to minimize the risks to bowhead whales as shipping and industrial fishing expand in the Arctic with ice retreat.     

Getting it right for the North Atlantic right whale (Eubalaenaglacialis): A last opportunity for effective marine spatial planning?

The North Atlantic right whale (Eubalaena glacialis) faces increasing pressure from commercial shipping traffic and proposed marine renewable energy developments. Drawing upon the successful Stellwagen Bank National Marine Sanctuary model, we propose a multi-stakeholder marine spatial planning process that considers both appropriate positioning of offshore wind farms and redefining commercial shipping lanes relative to whale migration routes: placement of wind turbines within certain right whale habitats may prove beneficial for the species. To that end, it may be advisable to initially relocate the shipping lanes for the benefit of the whales prior to selecting wind energy areas. The optimal end-state is the commercial viability of renewable energy, as well as a safe shipping infrastructure, with minimal risk of collision and exposure to shipping noise for the whales. This opportunity to manage impacts on right whales could serve as a model for other problematic interactions between marine life and commercial activities.     

High mercury levels in hair samples from residents of Taiji, a Japanese whaling town

We investigated the mercury concentrations in red meat from pilot whales consumed by some residents of the Japanese whaling town, Taiji, and in hair samples from 50 residents for their maker of mercury burden. The methyl mercury (M-Hg) level in the red meat was 5.9 μg/wet g, markedly higher than the US FDA action level and Cordex Alimentarius guideline level for predatory fish (1.0 μg/wet g). The average level of total mercury (T-Hg) in the hair from residents who ate whale meat more than once a month was 24.6 μg/g, whereas the average from the residents who did not consume any whale meat was 4.3 μg/g. The T-Hg concentrations in the hair from three donors exceeded 50 μg/g, the level for NOAEL set by WHO. The T-Hg level found in the Taiji whale meat consumers was markedly higher than that observed in the Japanese population overall (about 2 μg/g).     

Fatal ingestion of floating net debris by two sperm whales (Physeter macrocephalus)

In 2008 two male sperm whales (Physeter macrocephalus) stranded along the northern California coast with large amounts of fishing net scraps, rope, and other plastic debris in their stomachs. One animal had a ruptured stomach, the other was emaciated, and gastric impaction was suspected as the cause of both deaths. There were 134 different types of nets in these two animals, all made of floating material, varying in size from 10 cm² to about 16 m². The variability in size and age of the pieces suggests the material was ingested from the surface as debris rather than bitten off from active gear. These strandings demonstrate that ingestion of marine debris can be fatal to large whales, in addition to the well documented entanglements known to impact these species.