Population structure of blackfin tuna (Thunnus atlanticus) in the western Atlantic Ocean inferred from microsatellite loci.

The blackfin tuna, Thunnus atlanticus, is a small tropical tuna exploited by recreational and commercial fisheries in various parts of its range. Information on stock structure is needed to develop management plans for this species but is currently lacking. In this work, 470 blackfin tuna from nine geographic populations were assayed at 13 homologous microsatellite markers to provide a first assessment of stock structure across the species range. The overall divergence among locality samples was very low (overall FST = 0.0004) indicating high connectivity of blackfin tuna across their range. No clear grouping of localities in differentiated units was inferred but structuring followed a weak isolation by distance pattern (r = 0.16, P = 0.032). Pairwise exact tests and spatial analysis of molecular variance suggested divergence of the sample collected offshore Baía Formosa (Brazil) possibly reflecting reproductive isolation of Brazilian populations from those in the Caribbean region and further north. Further study of the status of Brazilian populations and the transition between this region and the Caribbean is warranted. Cryptic subdivision within the Northern Hemisphere part of the range is possible and should be evaluated using increased marker density and a more comprehensive geographic coverage.

Equatorial Atlantic pelagic predators reveal low content of PBDEs in contrast to MeO-BDEs: An analysis of brominated diphenyl ethers in blue shark and yellowfin tuna.

Polybrominated diphenyl ethers (PBDEs) and their methoxylated analogues (MeO-BDEs) are widely distributed in the environment. The main concern about the presence of PBDEs and MeO-BDEs in fish is due to their potential endocrine disruption effects in the specimens, and their potential risk to the health of human consumers. Considering these concerns, the goal of this study was to investigate the occurrence of PBDEs and MeO-BDEs in muscle tissues of blue shark (BSH), Prionace glauca, and yellowfin tuna (YFT), Thunnus albacares, caught in the Equatorial Atlantic Ocean (EAO), North-eastern Brazilian waters, and to evaluate the potential risk of human exposure by consumption. Muscle tissues of YFT and BSH were extracted using a Soxhlet apparatus and an Accelerated Solvent Extractor (ASE), respectively. PBDEs and MeO-BDEs were analysed by GC-NCI-MS. Concentrations of PBDEs ranged from not detected (nd) to 10 ng g-1 lipid weight (lw) in YFT muscle samples, while PBDE levels in BSH muscle samples ranged from

Morphological analysis and description of the ovaries of female silky sharks, Carcharhinus falciformis (Müller & Henle, 1839)

This work aims to study the female reproductive tract of silky sharks, Carcharhinus falciformis, captured in the South and Equatorial Atlantic Ocean. Samples were collected between January 2008 and March 2010 through oceanic commercial vessels that targeted tuna and swordfish, with a total of 17 females collected. The methodologies followed for analyzing the ovaries of those females included both macroscopic and histological analysis. Macroscopically, it was possible to determine that the ovaries on these sharks is suspended by mesenteries in the anterior section of the body cavity, heavily irrigated by blood vessels, and contains a wide range of oocytes. Ovaries were found in three distinct maturational stages: Stage I (Immature), Stage II (Maturing) and Stage III (Mature). Immature ovaries were small, with widths ranging from 1.0 to 3.1 cm, and had a gelatinous or granulose internal structure; maturing ovaries were slightly larger, ranging in width between 5.2 and 6.0 cm; mature ovaries ranged in width between 6.5 and 7.8 cm, and had a more rounded shape and the presence of large and well developed oocytes. Under microscopic examination, it was observed that the ovaries were covered with simple epithelial tissue during the early development stages and a simple cubic epithelium in the final stages of maturation. During the initial maturation stages the epigonal organ was not differentiated from the ovary. In mature specimens, the ovary showed a simple cubic epithelium and just below this epithelium there was a layer of dense connective tissue and muscle with the presence of vitellogenic oocytes and fat cells. A thin yolk membrane enclosing the oocytes was also evident. Finally, it was possible to distinguish a zona pellucida, separating the oocytes from the follicle wall and a basal lamina between the granular layers and the teak layer.

Este trabalho tem como objetivo estudar o trato reprodutivo feminino de tubarões lombo preto, Carcharhinus falciformis, capturados no Atlântico Sul e Equatorial. As amostras foram coletadas entre janeiro de 2008 e março de 2010, através das embarcações da frota atuneira, que tem como pesca alvo o atum e espadarte, com um total de 17 fêmeas coletadas. A metodologia seguida para analisar os ovários das fêmeas incluiu a análise macroscópica e histológica. Macroscopicamente, foi possível determinar que o ovário destes tubarões, é suspenso por mesentério na seção anterior da cavidade do corpo, muito irrigada por vasos sanguíneos, contendo uma vasta gama de ovócitos. Os ovários foram encontrados em três diferentes estágios de maturação: estádio I (imaturo), estágio II (maturação) e fase III (Maturo). Ovários imaturos foram pequenos, com largura variando de 1,0 a 3,1 centímetros, e tinham uma estrutura gelatinosa ou granulosa interna; ovários em maturação foram ligeiramente maiores, variando de largura entre 5,2 e 6,0 cm; ovários maduros variaram de largura entre 6,5 e 7,8 cm, possuíam uma forma mais arredondada e a presença de ovócitos grandes e bem desenvolvidos. Ao exame microscópico, foi possível observar que os ovários foram cobertos com tecido epitelial simples durante os estágios iniciais de desenvolvimento, e um epitélio cúbico simples na fase final de maturação. Durante os estágios iniciais de maturação, o órgão epigonal não foi diferenciado do ovário. Em espécimes maduros, o ovário mostrou um epitélio cúbico simples, e só abaixo deste epitélio havia uma camada de tecido conjuntivo denso e músculo com a presença de ovócitos vitelogênicos e células de gordura. Também foi evidenciada uma membrana fina juntando os ovócitos. Finalmente, foi possível distinguir uma zona pelúcida, separando os ovócitos da parede do folículo e uma lâmina basal entre as camadas granular e da camada teca.