Carlos Olavarría

Understanding morphological variation across geographic space is central to evolutionary and functional studies of marine vertebrates. Here, we examine variation in dorsal fin shape in the Commerson’s dolphin (Cephalorhynchus commersonii), a small coastal cetacean with a disjunct distribution across South America and the Kerguelen Islands. Dorsal fin shape was quantified using geometric morphometrics based on photographs, and comparisons were conducted across subspecies and populations. Principal Component Analysis revealed partial overlap in morphospace, with higher shape variability in the Kerguelen subspecies. Canonical Variate Analysis showed separation among geographic groups, although patterns of overlap remained. Differences in mean fin shape were observed among populations, particularly in the relative development of the free span and base of the fin. Kerguelen dolphins exhibited a relatively broader fin base and reduced free span, whereas South American populations generally showed a wider free span, with additional variation among regional populations. Morphological patterns did not fully correspond to population genetic structure, suggesting that multiple factors may contribute to phenotypic variation in this species. Similarities between geographically distant populations highlight the potential influence of shared environmental conditions. These results emphasize the value of dorsal fin morphology for investigating spatial variation in small cetaceans and provide a basis for future integrative studies combining ecological, physiological, and genetic data.

The 20 ^th century commercial whaling industry severely reduced populations of great whales throughout the Southern Hemisphere. The effect of this exploitation on genetic diversity and population structure remains largely undescribed. Here, we compare pre- and post-whaling diversity of mitochondrial DNA (mtDNA) control region sequences for three great whales in the South Atlantic, the blue, humpback and fin whale. Pre-whaling diversity is described from mtDNA extracted from bones collected near abandoned whaling stations, primarily from the South Atlantic island of South Georgia. These bones are known to represent the first stage of 20 ^th century whaling and thus pre-whaling diversity of these populations. Post-whaling diversity is described from previously published studies reporting large-scale sampling of living whales in the Southern Hemisphere. Despite relatively high levels of surviving genetic diversity in the post-whaling populations, we found evidence of a probable loss of mtDNA lineages in all three species. This is evidenced by the detection of a large number of haplotypes found in the pre-whaling samples that are not present in the post-whaling samples. A rarefaction analysis further supports a loss of haplotypes in the South Atlantic humpback and Antarctic blue whale populations. The bones from former whaling stations in the South Atlantic represent a remarkable molecular archive for further investigation of the decline and ongoing recovery in the great whales of the Southern Hemisphere.

Cetacean strandings are a valuable source of information for several studies from species richness to conservation and management. During the examination of strandings, taxonomic and sex identification might be hindered for several reasons. Molecular techniques are valuable tools to obtain that missing information. This study evaluates how gene fragment amplification protocols can support the records of strandings done in the field in Chile by identifying, corroborating, or correcting the identification of the species and sex of the recorded individuals. Through a collaboration between a scientific laboratory and government institution in Chile, 63 samples were analyzed. Thirty-nine samples were successfully identified to the species level. In total, 17 species of six families were detected, including six species of conservation interest. Of the 39 samples, 29 corresponded to corroborations of field identifications. Seven corresponded to unidentified samples and three to corrected misidentifications, adding up to 28% of the identified samples. Sex was successfully identified for 58 of the 63 individuals. Twenty were corroborations, 34 were previously unidentified, and four were corrections. Applying this method improves the stranding database of Chile and provides new data for future management and conservation tasks.

We analysed 114 DNA samples collected in different locations within the stock G breeding grounds, including Ecuador and the northern and southern Pacific of Colombia. We genotyped 15 microsatellite loci, sexed all samples, and performed genotype comparisons. Genotype comparisons were done using a DNA register of previously genotyped individuals from the Colombian breeding ground and the Antarctic Peninsula feeding Area. We confirmed connectivity between feeding grounds in Antarctic Peninsula and breeding grounds in Colombia and Ecuador using microsatellite loci. We found recaptures within each sampling location in the same year, but we also found a few recaptures in the same locations between years both in breeding and feeding grounds. Interestingly, we found recaptures between breeding and feeding grounds using samples collected 20 years apart, providing some information about longevity in this stock. Further comparisons with other data sets (Brazil, North Pacific) are needed to understand the migratory connectivity of this stock.