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Two major ecological transitions marked the history of the Black Sea after the last Ice Age. The first was the postglacial transition from a brackish-water to a marine ecosystem dominated by porpoises and dolphins once this basin was reconnected back to the Mediterranean Sea (ca. 8,000 y B.P.). The second occurred during the past decades, when overfishing and hunting activities brought these predators close to extinction, having a deep impact on the structure and dynamics of the ecosystem. Estimating the extent of this decimation is essential for characterizing this ecosystem's dynamics and for formulating restoration plans. However, this extent is poorly documented in historical records. We addressed this issue for one of the main Black Sea predators, the harbor porpoise, using a population genetics approach. Analyzing its genetic diversity using an approximate Bayesian computation approach, we show that only a demographic expansion (at most 5,000 y ago) followed by a contemporaneous population collapse can explain the observed genetic data. We demonstrate that both the postglacial settlement of harbor porpoises in the Black Sea and the recent anthropogenic activities have left a clear footprint on their genetic diversity. Specifically, we infer a strong population reduction (∼90%) that occurred within the past 5 decades, which can therefore clearly be related to the recent massive killing of small cetaceans and to the continuing incidental catches in commercial fisheries. Our study thus provides a quantitative assessment of these demographically catastrophic events, also showing that two separate historical events can be inferred from contemporary genetic data.conservation biology | demographic inference | coalescence | Bayesian analyses

Cetacean stranding reports in the North Aegean Sea were recorded since 1998 from Strimonikos Gulf in Chalkidiki up to Alexandroupoli on the Turkish border and in a few northern Aegean islands. On site, the specimens were examined to identify species, gender, approximate age and, when possible, cause for stranding. A total of 26 filled stomachs of five cetacean species collected since 2002 were analysed: bottlenose dolphinsTursiops truncatus(N = 8), common dolphinsDelphinus delphis(N = 8), harbour porpoisesPhocoena phocoena(N = 5), striped dolphinsStenella coeruleoalba(N = 4) and Risso's dolphinsGrampus griseus(N = 1). From the analysed stomachs it was found that the bottlenose dolphins fed mainly on snake blennyOphidion barbatum(34%), bogueBoops boops(22%) and round sardinellaSardinella aurita(13%); common dolphins on round sardinella (17%), picarelsSpicaraspp. (10%) and Cocco's lantern fishLobianchia gemellaris(9%); harbour porpoises on Gobidae (four-spotted gobyDeltentosteus quadrimaculatus41% and black gobyGobius niger37%) and round sardinella (7%); striped dolphins on Myctophydae (Madeira lantern fishCeratoscopelus maderensis51%), and on Pfeffer's enople squidAbraliopsis morisii(10%) and bogue (8%); and Risso's dolphin exclusively on Teuthidae (31%), the umbrella squidHistioteuthis bonellii(30%) and the reverse jewel squidH. reversa(14%). The present work represents the first attempt to investigate the diet up to species level for several cetaceans in Greek waters and for harbour porpoises stranded in the Mediterranean Sea.

SUMMARY: The round sardinella, Sardinella aurita Valenciennes, 1847, was sampled monthly from commercial purseseine vessels in Kavala Gulf (northern Aegean Sea, Greece) for two complete year cycles (September 2000-August 2002. Its maximum total length and age were 248 mm and 5 years respectively. The length-weight relationship was W=0.0062TL 3.064 for males and W=0.0059TL 3.084 for females. The marginal increment analysis on scales (n=1352) confirmed annulus formation during February-March, which coincided with the lowest sea surface temperature prevailing in the study area. The marginal increment ratio for ages 1, 2 and 3 was positively correlated with sea surface temperature (all r>0.4, P<0.05). The parameters of the von Bertalanffy growth equation were: L ∞ =248.678 mm, K=0.509 yr -1 and t 0 =-0.881 yr. The comparison of growth parameters for round sardinella, using the auximetric plot, from Mediterranean and northwest African waters indicated different growth patterns between the two areas.

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