An auditory study was conducted to derive data on temporary threshold shift (TTS) induced by single impulses. This information should serve as basis for the definition of noise exposure criteria for harbor porpoises. The measurements of TTS were conducted on a harbor porpoise by measuring the auditory evoked potentials in response to amplitude-modulated sounds. After obtaining baseline hearing data the animal was exposed to single airgun stimuli at increasing received levels. Immediately after each exposure the animal's hearing threshold was tested for significant changes. The received levels of the airgun impulses were increased until TTS was reached. At 4 kHz the predefined TTS criterion was exceeded at a received sound pressure level of 199.7 dB(pk-pk) re 1 microPa and a sound exposure level (SEL) of 164.3 dB re 1 microPa(2) s. The animal consistently showed aversive behavioral reactions at received sound pressure levels above 174 dB(pk-pk) re 1 microPa or a SEL of 145 dB re 1 microPa(2) s. Elevated levels of baseline hearing sensitivity indicate potentially masked acoustic thresholds. Therefore, the resulting TTS levels should be considered masked temporary threshold shift (MTTS) levels. The MTTS levels are lower than for any other cetacean species tested so far.
SUMMARYPorpoise echolocation has been studied previously, mainly in target detection experiments using stationed animals and steel sphere targets, but little is known about the acoustic behaviour of free-swimming porpoises echolocating for prey. Here, we used small onboard sound and orientation recording tags to study the echolocation behaviour of free-swimming trained porpoises as they caught dead, freely drifting fish. We analysed porpoise echolocation behaviour leading up to and following prey capture events, including variability in echolocation in response to vision restriction, prey species, and individual porpoise tested. The porpoises produced echolocation clicks as they searched for the fish, followed by fast-repetition-rate clicks (echolocation buzzes) when acquiring prey. During buzzes, which usually began when porpoises were about 1-2 body lengths from prey, tag-recorded click levels decreased by about 10 dB, click rates increased to over 300 clicks per second, and variability in body orientation (roll) increased. Buzzes generally continued beyond the first contact with the fish, and often extended until or after the end of prey handling. This unexplained continuation of buzzes after prey capture raises questions about the function of buzzes, suggesting that in addition to providing detailed information on target location during the capture, they may serve additional purposes such as the relocation of potentially escaping prey. We conclude that porpoises display the same overall acoustic prey capture behaviour seen in larger toothed whales in the wild, albeit at a faster pace, clicking slowly during search and approach phases and buzzing during prey capture.
Changes in fish distribution are being observed across the globe. In Europe's Common Fisheries Policy, the share of the catch of each fish stock is split among management areas using a fixed allocation key known as ‘Relative Stability’: in each management area, member states get the same proportion of the total catch each year. That proportion is largely based on catches made by those member states in the 1970s. Changes in distribution can, therefore, result in a mismatch between quota shares and regional abundances within management areas, with potential repercussions for the status of fish stocks and the fisheries that depend on them. Assessing distribution changes is crucial to ensure adequate management and sustainable exploitation of our fish resources. We analysed scientific survey data using a three‐tiered analytical approach to provide, for the first time, an overview of changes in distribution for 19 northeast Atlantic fish species encompassing 73 commercial stocks over 30 yr. All species have experienced changes in distribution, five of which did so across management areas. A cross‐species analysis suggested that shifts in areas of suitable thermal habitat, and density‐dependent use of these areas, are at least partly responsible for the observed changes. These findings challenge the current use of relative stability to allocate quotas.
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Killer whales Orcinus orca have a cosmopolitan distribution with a broad diet ranging from fish to marine mammals. In Norway, killer whales are regularly observed feeding on overwintering Norwegian spring-spawning (NSS) herring Clupea harengus inside the fjords. However, their offshore foraging behavior and distribution are less well understood. In particular, it is not known to what degree they rely on the NSS herring stock when the herring move to deeper offshore waters. Satellite telemetry data from 29 male killer whales were analyzed to assess whether their offshore foraging behavior is linked to herring distribution. Unlike most marine predator-prey studies that use indirect proxies for prey abundance and distribution, our study utilized 2 herring density estimates based on (1) direct observations from acoustic trawl survey data and (2) simulations from a fully coupled ecosystem model. Mixed effects models were used to infer the effect of herring density and light intensity on whale movement patterns. Our results suggest that killer whales follow NSS herring over long distances along the coast from their inshore overwintering areas to offshore spawning grounds. All whales changed from fast, directed, to slow, non-directed movement when herring density increased, although individuals had different propensities towards movement. Our data indicated that whales continue to feed on herring along the Norwegian shelf. We conclude that NSS herring constitute an important prey resource for at least some killer whales in the northeastern Atlantic, not only during the herring overwintering period, but also subsequently throughout the herring spawning migration.
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