Despite frequent records from other parts of the North Atlantic, minke whales have never been acoustically recorded in the North Sea. This study investigated the detectability of pulse trains previously associated with this species in other regions, in acoustic data from ten sites along the east coast of Scotland. Since preliminary results confirmed pulse train presence, subsequently, an automated detector was applied to these data to record the seasonal and diel presence of minke whale pulse trains. Minke whales were detected from May to November, with most detections occurring in June, July and October. No acoustic detections were made in December, January or in the month of April, whilst no data were available for February and March. This pattern of acoustic presence supports available visual data and suggested an absence of minke whales from the study area during winter. Minke whale acoustic presence showed a statistically significant diel pattern, with a detection peak during night time. This study established the acoustic detectability of minke whales in the North Sea and highlights the potential of using passive acoustic monitoring to study the seasonal presence and spatial distribution of minke whales in the North Sea and wider Northeast Atlantic.
Here we present a comparison of saddle and eye patch patterns of killer whales from Norwegian, Icelandic, British, Spanish and Greenlandic waters. We found only a small amount of variation in saddle patch shapes, which may reflect a recent phylogenetic divergence from the most recent common ancestor. Eye patch shapes were more variable than saddle patches in small details. Most individuals had eye patches with parallel orientation, with the exception of a small group of killer whales from the Hebrides, which, as previously reported, had sloping eye patches that sloped downward at the posterior end. This differentiation in pigmentation patterns of the Hebridean killer whales from neighbouring populations could reflect one or more of several evolutionary processes, including a deeper phylogenetic divergence, low gene flow with other local populations and drift.
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