The foraging ecology of endangered olive ridley Lepidochelys olivacea sea turtles is poorly known in Australia, with only a limited knowledge of their foraging distribution inferred from captures in trawl net fisheries. We attached satellite transmitters to 8 olive ridley turtles in 2004 and 2005 at a nesting beach in Australia's Northern Territory to document their migratory routes and foraging behaviour. Three turtles moved up to 40 km from the nesting beach before renesting on the same beach within 12 to 23 d. The turtles made post-nesting migrations of 165 to 1050 km to 5 different foraging areas and used coastal, continental shelf and continental slope habitats. The use of one foraging area by 3 turtles, together with previous trawl data, indicate a predictable source of food in this area. Distinct foraging areas indicate that foraging behaviour differs from the meandering oceanic movements of turtles in the Pacific. During migration and foraging periods, turtles dived to the substrate with maximum depths of 150 to 200 m and maximum dive durations of 120 to 180 min. The locations of foraging areas overlapped with existing trawl fisheries and oil and gas exploration and mining.

Background: Quantifying primary sex ratios is essential for assessing how global warming will influence the population dynamics of species with temperature-dependent sex determination (TSD). Process-explicit (mechanistic) models can accurately estimate primary sex ratios but require the resolution of the key physiological parameters that influence sex determination and validation of the model by testing predictions against empirical data.Results: To address these goals, we conducted incubation experiments on flatback sea turtle (Natator depressus) embryos from a large winter-nesting rookery at Cape Domett in the East Kimberley region of Western Australia. A TSD model fitted to laboratory and field nest data indicated that the pivotal temperature producing equal sex ratios was 29.4°C, with males produced below 27.7°C and females produced above 31.1°C. Back-switch experiments revealed that the thermosensitive period (TSP), when gonads differentiate into testes or ovaries, occurs between 43% and 66% of development to hatching. Integrating this new information with sand temperatures reconstructed from 23 years of historical climate data shows that male-biased sex ratios are likely if the TSP falls during the Austral winter. Annual variation in the simulated sand temperatures increased from 1990 to 2013, with cooler winters producing conditions that favoured male hatchlings for longer periods. The same model projected to 2030 and 2070 suggests that femalebiased primary sex ratios will become more prevalent over time. Conclusions: Our results show that accurate modelling of primary sex ratios depends on quantifying the thermal biology of embryos and on parameterising mechanistic models of sand temperatures with site-specific climate data.

Identification of the geographic extent of population boundaries, the distribution of genetic lineages, and the amount of genetic exchange among breeding groups is needed for effective conservation of vulnerable marine migratory species. This is particularly true of the flatback turtle (Natator depressus), which only breeds in Australia but has extensive migrations that can include international waters. This study investigated the phylogeography and genetic structure among 17 flatback turtle rookeries across their range by sequencing an 810 bp portion of the mitochondrial DNA in 889 samples and genotyping 10 microsatellite loci in 598 samples. There was low phylogenetic divergence among haplotypes and evidence of recent population expansion, likely in the late Pleistocene. A predominant haplotype was found across all rookeries, but other haplotype groups were regionally specific. In general, there was agreement in patterns of genetic differentiation in the mitochondrial DNA and microsatellite data, and in some pairwise comparisons a higher mutation rate of microsatellites provided stronger evidence of differentiation. These results suggest natal philopatry operates in the choice of breeding locations for males as well as females. Evidence of genetic connectivity among neighbouring rookeries led to the identification of seven genetic stocks. Geographic boundaries of rookeries used by genetic stocks varied widely (160–1,300 km), highlighting a need for field studies to better understand movement patterns. Hierarchical analysis of molecular variance identified significant genetic differentiation based upon genetic stock, nesting phenology (summer vs. winter nesters), and a west–east discontinuity across Torres Strait. A pattern of isolation by distance was identified, which was most strongly observed in the microsatellite data. In combination with tagging and telemetry studies, these results will allow better quantification of stock‐specific threats along migratory routes and in foraging habitats. Implications of climate change will be stock specific and may depend upon the extent of genetic connectivity between neighbouring stocks.

Globally distributed marine taxa are well suited for investigations of biogeographic impacts on genetic diversity, connectivity, and population demography. The sea turtle genus Lepidochelys includes the wide-ranging and abundant olive ridley (L. olivacea), and the geographically restricted and ‘Critically Endangered’ Kemp’s ridley (L. kempii). To investigate their historical biogeography, we analyzed a large dataset of mitochondrial DNA (mtDNA) sequences from olive (n = 943) and Kemp’s (n = 287) ridleys, and genotyped 15 nuclear microsatellite loci in a global sample of olive ridleys (n = 285). We found that the ridley species split ~ 7.5 million years ago, before the Panama Isthmus closure. The most ancient mitochondrial olive ridley lineage, located in the Indian Ocean, was dated to ~ 2.2 Mya. Both mitochondrial and nuclear markers revealed significant structure for olive ridleys between Atlantic (ATL), East Pacific (EP), and Indo-West Pacific (IWP) areas. However, the divergence of mtDNA clades was very recent (< 1 Mya) with low within- clade diversity, supporting a recurrent extinction-recolonization model for these ocean regions. All data showed that ATL and IWP groups were more closely related than those in the EP, with mtDNA data supporting recent recolonization of the ATL from the IWP. Individual olive ridley dispersal between the ATL, EP, and IN/IWP could be interpreted as more male- than female-biased, and genetic diversity was lowest in the Atlantic Ocean. All populations showed signs of recent expansion, and estimated time frames were concordant with their recent colonization history. Investigating species abundance and distribution changes over time is central to evolutionary biology, and this study provides a historical biogeographic context for marine vertebrate conservation and management.

No abstract