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Stable isotope analysis of baleen plates is a widespread technique for studying baleen whales. Typically, subsamples along the growth axis of the baleen plate are extracted and analysed to examine time-related variation in their stable isotope signals. However, baleen plate tissue is composed of two different tissues: a pair of cortex layers flanking an internal medulla. These two histological components exhibit differential development, and their consolidation as a tissue is therefore likely non-synchronic. This could influence stable isotope results because the stable isotope signal may differ in each subsample according to the proportion of the two histological components extracted from the tissue. In this study, stable isotope analysis was combined with optical microscopy examination of fin whale (Balaenoptera physalus) baleen plates to understand the ontogeny of the two histological components. In both of them, the δ15N values followed a sinewave pattern along the growth axis of the baleen plate. However, the δ15N values of the cortex appeared to be advanced compared to those of the medulla. Additionally, the amplitude of the δ15N values in the oscillations was higher in the cortex than in the medulla. The histological examination revealed that these differences are caused by earlier and faster synthesis of the cortex layer compared to that of the medulla. Because the stable isotope ratios of the two layers differ, we propose that in this type of studies only the outer-most part (closest to the surface) of the cortex should be subsampled and analysed. Additionally, to include the most recently formed tissue, this subsampling should start well below the zwischensubstanz, or baleen "gum". [ABSTRACT FROM AUTHOR]

Stable isotope analysis of baleen plates is a widespread technique for studying baleen whales. Typically, subsamples along the growth axis of the baleen plate are extracted and analysed to examine time-related variation in their stable isotope signals. However, baleen plate tissue is composed of two different tissues: a pair of cortex layers flanking an internal medulla. These two histological components exhibit differential development, and their consolidation as a tissue is therefore likely non-synchronic. This could influence stable isotope results because the stable isotope signal may differ in each subsample according to the proportion of the two histological components extracted from the tissue. In this study, stable isotope analysis was combined with optical microscopy examination of fin whale (Balaenoptera physalus) baleen plates to understand the ontogeny of the two histological components. In both of them, the δ15N values followed a sinewave pattern along the growth axis of the baleen plate. However, the δ15N values of the cortex appeared to be advanced compared to those of the medulla. Additionally, the amplitude of the 815N values in the oscillations was higher in the cortex than in the medulla. The histological examination revealed that these differences are caused by earlier and faster synthesis of the cortex layer compared to that of the medulla. Because the stable isotope ratios of the two layers differ, we propose that in this type of studies only the outer-most part (closest to the surface) of the cortex should be subsampled and analysed. Additionally, to include the most recently formed tissue, this subsampling should start well below the zwischensubstanz, or baleen "gum". [ABSTRACT FROM AUTHOR]

[Display omitted] • δ13C, δ15N and δ34S were analysed in skin from 5 Icelandic baleen whale species. • MixSiar model showed that krill was the main prey for all species except common minke whales. • In humpback whales, dependence on krill may reduce entanglement risk in fishing gear. • Isotopic niche overlap between species was small, except between blue and fin whales. • Niche overlap between fin and blue whales suggests strong interspecific competition. The highly productive waters off Iceland are an important feeding ground for baleen whales. Five balaenopterid species coexist there during the summer feeding season: the blue whale, the fin whale, the sei whale, the humpback whale and the common minke whale. For capital breeders such as baleen whales, niche partitioning and reduced interspecific competition during their stay in the feeding grounds may be critical for the completion of their annual cycles and the long-term stability of populations. Coexistence often entails spatio-temporal or trophic segregation to avoid competitive exclusion. With the aim of studying how these species share habitat and trophic resources, we analyzed the δ13C, δ15N and δ34S values in skin samples. Bayesian stable isotope mixing models to calculate compositional mixture of food sources showed that most species segregate by consuming different prey. Segregation was further enhanced by some degree of spatio-temporal exclusion. Overall, clear ecological niche partitioning was apparent between all species except between blue and fin whales. All the species consumed krill and, except for the common minke whale, this was the dominant prey. Among baleen whales, common minke whales and humpback whales were the major predators of sand eel, capelin and herring. In humpback whales, a strong reliance on krill may explain the apparently low rates of local entanglement in fishing nets as compared to other areas. Except for the blue whale, all species have shown evidence of adapting to shifts in prey availability and thus suggested capacity to cope with variability. However, in a scenario of increasing environmental variability associated to global warming, the overlap between ecological niches may have to decrease to allow long-term coexistence. [ABSTRACT FROM AUTHOR]