The North Atlantic Sightings Survey (NASS), the sixth in a series of surveys conducted between 1987 and 2015, was conducted in June/July 2015 and covered a large area of the northern North Atlantic. The Icelandic and Faroese ship survey component of the NASS covered the area between the Faroe Islands and East Greenland from latitude 52° to 72° N. The survey used 3 vessels and an independent double-platform configuration with each platform staffed by a minimum of 2 observers. Here we present both uncorrected abundance estimates derived using Multiple Covariates Distance Sampling, and corrected abundance estimates derived using Mark-Recapture Distance Sampling, for the following species: fin (Balaenoptera physalus), common minke (B. acutorstrata), humpback (Megaptera novaeangliae), blue (B. musculus), sei (B. borealis), sperm (Physeter macrocephalus), long-finned pilot (Globicephala melas) and northern bottlenose (Hyperoodon ampullatus) whales as well as white-beaked (Lagenorhynchus albirostris) and white-sided (L. acutus) dolphins. We then compare these estimates to those from previous NASS and put them into context with estimates from adjoining areas of the North Atlantic.
It is generally recognized that large-scale whaling in the 19th and 20th century led to a substantial reduction of the size of many cetacean populations, particularly those of the baleen whales (Mysticeti). The impact of these operations on genomic diversity of one of the most hunted whales, the fin whale (Balaenoptera physalus), has remained largely unaddressed, because of the paucity of adequate samples and the limitation of applicable techniques. Here, we have examined the effect of whaling on the North Atlantic fin whale based on genomes of 51 individuals from Icelandic waters, representing three temporally separated intervals, 1989, 2009 and 2018 and provide a reference genome for the species. Demographic models suggest a noticeable drop of the effective population size of the North Atlantic fin whale around a century ago. The present results suggest that the genome-wide heterozygosity is not markedly reduced and has remained comparable to other baleen whale species. Similarly, there are no signs of apparent inbreeding, as measured by the proportion of long runs of homozygosity, or of a distinctively increased mutational load, as measured by the amount of putative deleterious mutations. Compared to other baleen whales, the North Atlantic fin whale appears to be less affected by anthropogenic influences than other whales such as the North Atlantic right whale, consistent with the presence of long runs of homozygosity and higher levels of mutational load in an otherwise more heterozygous genome. Thus, genome-wide assessments of other species and populations are essential for future, more specific, conservation efforts.
The Trans-North Atlantic Sightings Survey (T-NASS) carried out in June-July 2007 was the fifth in a series of large-scale cetacean surveys conducted previously in 1987, 1989, 1995 and 2001. The core survey area covered an area of about 1.8 million nm² spanning from the Eastern Barents Sea at 34°E to the east coast of Canada, and between 52°N and 78°N in the east and south to 42°N in the west. We present design-based abundance estimates from the Faroese and Icelandic vessel survey components of T-NASS, as well as results from ancillary vessels which covered adjoining areas. The 4 dedicated survey vessels used a Buckland-Turnock (B-T) mode with a tracker platform searching an area ahead of the primary platform and tracking sightings to provide data for bias correction. Both uncorrected estimates, using the combined non-duplicate sightings from both platforms, and mark-recapture estimates, correcting estimates from the primary platform for bias due to perception and availability, are presented for those species with a sufficient number of sightings. Corrected estimates for the core survey area are as follows: fin whales (Balaenoptera physalus): 30,777 (CV=0.19); humpback whales (Megaptera novaeangliae): 18,105 (CV=0.43); sperm whales (Physeter macrocephalus): 12,268 (CV=0.33); long-finned pilot whales (Globicephala melas): 87,417 (CV=0.38); white-beaked dolphins (Lagenorhynchus albirostris): 91,277 (CV=0.53); and white-sided dolphins (L. acutus): 81,008 (CV=0.54). Uncorrected estimates only were possible for common minke whales (B. acutorstrata): 12,427 (CV=0.27); and sei whales (B. borealis): 5,159 (CV=0.47). Sighting rates from the ancillary vessels, which used a single platform, were lower than those from the dedicated vessels in areas where they overlapped. No evidence of responsive movement by any species was detected, but there was some indication that distance measurements by the primary platform may have been negatively biased. The significance of this for the abundance estimates is discussed. The relative merits of B-T over other survey modes are discussed and recommendations for future surveys are provided.
A total of 1,268 harbour porpoises were obtained from fishing nets in Icelandic coastal waters from September to June in the years 1991 to 1997. Foetal sex ratio was 1.2:1 (male:female). The bias towards males increased further among older animals in the present collection. The modal year classes were 0 and 1 years but the oldest porpoise was a female estimated at 20 years of age. Length at birth was estimated as approximately 75 cm, and females grew faster and attained larger sizes than males. Asymptotic length was 149.6 cm for males and 160.1 cm for females. Estimated age and length at sexual maturity was 1.9 to 2.9 years and 135 cm for males and 2.1 to 4.4 years and 138 to 147 cm for females. Immature individuals were significantly shorter than pubertal and mature animals in both sexes in age classes 1 to 3. Testes weight increased only slightly with body size in immature males but increased rapidly around maturity. Pronounced seasonality was also observed in testes weight, indicating a peak in testes activity in summer. Lack of data from the summer makes the exact timing of parturition and mating unknown. Births do, however, most likely peak in June and July and lactation lasts at least 7 to 8 months. Ovulation and pregnancy rates were 0.98.
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