Diagnóstico da pesca no litoral do Parque Nacional do Cabo Orange e sua área circundante, município de Oiapoque estado do Amapá

O estado do Amapá apresenta-se com 70 % dos seus 14.281.458,5 ha de extensão transformados em áreas protegidas, entres as várias categorias de Unidades de Conservação e terras indígenas, por sua vez, muitas dessas áreas adentras as águas litorâneas do atlântico, ora pelos seus limites, ora pelos seus entornos (área circundante), tornando conflitante a atividade pesqueira na linha da costa amapaense. O Acordo de Pesca assinado em 2007 entre pescadores do município do Oiapoque e gerencia do Parque Nacional do Cabo Orange (ICMBIO) busca o controle das pescarias pela frota do Oiapoque e diminuir conflito na faixa de 20 km em águas marinhas, que pertencem ao seu limite e área circundante. Este estudo investigou as características da pesca na região do estuário do rio Oiapoque, faixa marinha do Parque e sua área circundante. A metodologia contemplou entrevistas formais e informais de vários atores do setor pesqueiro no Oiapoque, monitoramento de 488 desembarques e viagens aos locais de pescarias. Foram obtidas as CPUE’s em função do rendimento por dia de pesca por pescador (Kg/dia/pesca para cada tipo de embarcação). Foram mapeados os pesqueiros considerados importantes e tradicionalmente explorados pela frota do Oiapoque, dentro dos limites do Parque Nacional do Cabo Orange e em sua área circundante. Os pescadores do município realizam pescarias de subsistência, artesanal de menor e maior escala. Por sua vez, são as pescarias artesanais de menor escala que predominam na área do parque particularmente as embarcações do tipo “barco de pequeno porte” (BPP), que se destacaram em número, cerca de 60 % das cadastradas na colônia. O volume de pescado desembarcado no município do Oiapoque foi 766 toneladas no ano de 2008. São principalmente alvo das pescarias a corvina (Cynoscion virescens) e a pescada branca (Plagioscion spp), desta capturada de pescarias de menor escala, principalmente em embarcações de capacidade até 1 tonelada do tipo barco motorizado (BOM). A produção é comercializada diretamente dos pescadores para intermediários (balanceiros) que por sua vez, vendem para o mercado local, os dois grandes centros consumidores do Amapá (Macapá e Santana) e para outros estados (Pará, São Paulo etc).

Pesquisa de helmintos em musculatura e serosa abdominal de peixes de importância comercial capturados no litoral norte do Brasil

Com o objetivo de pesquisar a presença de helmintos, suas freqüências e intensidades de infecções, na musculatura e serosa abdominal parietal de peixes de importância comercial beneficiados em Belém-PA, foram examinados 175 exemplares de quatro espécies de peixes capturados no litoral norte do Brasil, sendo três espécies marinhas da Família Sciaenidae – a pescada amarela (Cynoscion acoupa), a pescada-cambuçú (Cynoscion virescens) e a pescadinha-gó ou pescada-foguete (Macrodon ancylodon); e um siluriforme estuarino da Família Ariidae - a uritinga (Arius proops). Os peixes foram mensurados quanto ao seu comprimento corporal padrão, analisou-se a musculatura e a serosa abdominal em mesa de inspeção “candling table” após o filetamento das amostras. Foi encontrado apenas parasitismo por larvas plerocercóides de cestóides da Ordem Trypanorhyncha. Os blastocistos recuperados foram observados quanto a sua morfologia e tamanho, sendo o mesmo realizado com os escólices após a sua liberação. Todas as espécies de peixes analisadas apresentavam indivíduos parasitados, sendo 16% em M. ancylodon, 77,78% em A. proops, 79,17% em C. virescens e 82% em C. acoupa, correspondendo uma freqüência parasitária geral de 61,71% (108 exemplares) e uma intensidade média de infecção de aproximadamente seis larvas por peixe. As freqüências de infecção apresentadas pelas espécies de cestóides foram as seguintes: Callitetrarhynchus gracilis (52,57%), Pterobothrium heteracanthum (13,71%), Poecilancistrium caryophyllum (12%) e Pterobothrium crassicolle (3,43%). Entre os peixes parasitados, 85,19% apresentavam parasitismo na região abdominal (serosa e musculatura abdominal) e 81,48% parasitismo muscular (musculatura abdominal e corporal). A espécie P. heteracanthum preferencialmente parasitou a região abdominal dos peixes e a espécie P. caryophyllum a musculatura. Verificou-se associação significativa (P < 0,01) entre as espécies de peixes analisadas e a freqüência de parasitismo.

A pesca de curral no município de São Caetano de Odivelas-PA

A pesca de curral é uma das artes de pesca mais tradicionais e produtivas da costa paraense e com uma produção que chega a representar 10% da produção pesqueira do Nordeste paraense (Santos et al., 2005). Sua produtividade depende tanto do modo como o curral é feito quanto do local onde é instalado. Para a realização desse trabalho, 12 currais de pesca foram selecionados em relação ao tipo (coração, enfia e cachimbo), ao local de instalação (“de beira” ou “de fora”) e ao tipo de ambiente em que se encontra (beira de rio, beira de praia e banco de areia), foram georreferenciados e tiveram sua produtividade pesqueira acompanhada durante o período de safra (junho, julho e agosto) de 2012. Na comunidade de São João de Ramos, foram monitorados 3 currais de beira do tipo coração, instalados as margens do rio Paruipema, e 3 currais de fora do tipo enfia, instalados em bancos de areia nas praias do rato e do marinheiro. Na comunidade do Aê, foram monitorados os 6 currais classificados como currais de beira, sendo 3 do tipo coração e 3 do tipo cachimbo, e todos se encontravam instalados na praia Ponta de Itaipu. Foram capturados 4.274 indivíduos, distribuídos em 9 ordens, 20 famílias e 43 espécies de peixes. A ordem Perciformes foi a que apresentou o maior número de famílias (10 famílias ou 50% do total), o maior número de espécies (19 ou 44%) e o maior número de indivíduos (3.190 ou 75% do total). As famílias Sciaenidae e Ariidae são as mais abundantes na região tanto em número de espécies quanto em indivíduos. A família Sciaenidae foi a que apresentou o maior número de indivíduos (2.855 ou 67%), mas apresentou menos espécies (8 ou 19%) que a família Ariidae, com 10 espécies ou 23% do total. Das 43 espécies capturadas, as quatro mais representadas foram: Macrodon ancylodon (51%), Arius couma (9%), Cynoscion virescens (9%) e Mugil incilis (4%). A comparação da captura entre os currais e localidades ao longo dos meses de monitoramento indicou que a produção total dos currais diferiu entre os tipos de currais associados com sua localidade.

Permanent Genetic Resources added to Molecular Ecology Resources Database 1 December 2011-31 January 2012

This article documents the addition of 473 microsatellite marker loci and 71 pairs of single-nucleotide polymorphism (SNP) sequencing primers to the Molecular Ecology Resources Database. Loci were developed for the following species: Barteria fistulosa, Bombus morio, Galaxias platei, Hematodinium perezi, Macrocentrus cingulum Brischke (a.k.a. M.abdominalis Fab., M.grandii Goidanich or M.gifuensis Ashmead), Micropogonias furnieri, Nerita melanotragus, Nilaparvata lugens Stal, Sciaenops ocellatus, Scomber scombrus, Spodoptera frugiperda and Turdus lherminieri. These loci were cross-tested on the following species: Barteria dewevrei, Barteria nigritana, Barteria solida, Cynoscion acoupa, Cynoscion jamaicensis, Cynoscion leiarchus, Cynoscion nebulosus, Cynoscion striatus, Cynoscion virescens, Macrodon ancylodon, Menticirrhus americanus, Nilaparvata muiri and Umbrina canosai. This article also documents the addition of 116 sequencing primer pairs for Dicentrarchus labrax.

Evolutionary associations between sand seatrout (Cynoscion arenarius) and silver seatrout (C. nothus) inferred from morphological characters, mitochondrial DNA, and microsatellite markers

The evolutionary associations between closely related fish species, both contemporary and historical, are frequently assessed by using molecular markers, such as microsatellites. Here, the presence and variability of microsatellite loci in two closely related species of marine fishes, sand seatrout (Cynoscion arenarius) and silver seatrout (C. nothus), are explored by using heterologous primers from red drum (Sciaenops ocellatus). Data from these loci are used in conjunction with morphological characters and mitochondrial DNA haplotypes to explore the extent of genetic exchange between species offshore of Galveston Bay, TX. Despite seasonal overlap in distribution, low genetic divergence at microsatellite loci, and similar life history parameters of C. arenarius and C. nothus, all three data sets indicated that hybridization between these species does not occur or occurs only rarely and that historical admixture in Galveston Bay after divergence between these species was unlikely. These results shed light upon the evolutionary history of these fishes and highlight the genetic properties of each species that are influenced by their life history and ecology.

Spatial and seasonal abundance of sand seatrout (Cynoscion arenarius) and silver seatrout (C. nothus) off the coast of Texas, determined with twenty years of data (1987–200

Sand seatrout (Cynoscion arenarius) and silver seatrout (C. nothus) are both found within the immediate offshore areas of the Gulf of Mexico, especially around Texas; however information is limited on how much distributional overlap really occurs between these species. In order to investigate spatial and seasonal differences between species, we analyzed twenty years of bay and offshore trawl data collected by biologists of the Coastal Fisheries Division, Texas Parks and Wildlife Department. Sand seatrout and silver seatrout were distributed differently among offshore sampling areas, and salinity and water depth appeared to correlate with their distribution. Additionally, within the northernmost sampling area of the gulf waters, water depth correlated significantly with the presence of silver seatrout, which were found at deeper depths than sand seatrout. There was also an overall significant decrease in silver seatrout abundance during the summer season, when temperatures were at their highest, and this decrease may have indicated a migration farther offshore. Sand seatrout abundance had an inverse relationship with salinity and water depth offshore. In addition, sand seatrout abundance was highest in bays with direct passes to the gulf and correlated with corresponding abundance in offshore areas. These data highlight the seasonal and spatial differences in abundance between sand and silver seatrout and relate these differences to the hydrological and geological features found along the Texas coastline.

Genetic variability in spotted seatrout (Cynoscion nebulosus), determined with microsatellite DNA markers

Variation in the allele frequencies of five microsatellite loci was surveyed in 1256 individual spotted seatrout (Cynoscion nebulosus) obtained from 12 bays and estuaries from Laguna Madre, Texas, to Charlotte Harbor, Florida, to St. John’s River on the Florida Atlantic Coast. Texas and Louisiana collection sites were resampled each year for two to four years (1998−2001). Genetic differentiation was observed. Spotted seatrout from Florida waters were strongly differentiated from spotted seatrout collected in Louisiana and Texas. The greatest genetic discontinuity was observed between Tampa Bay and Charlotte Harbor, and Charlotte Harbor seatrout were most similar to Atlantic Coast spotted seatrout. Texas and Louisiana samples were not strongly structured within the northwestern Gulf of Mexico and there was little evidence of temporal differentiation within bays. These findings are contrary to those of earlier analyses with allozymes and mitochondrial DNA (mtDNA) where evidence of spatial differentiation was found for spotted seatrout resident on the Texas coast. The differences in genetic structure observed among these markers may reflect differences in response to selective pressure, or may be due to differences in underlying genetic processes.

Feeding habits of the dwarf weakfish (Cynoscion nannus) off the coasts of Jalisco and Colima, Mexico

Sciaenids from the Pacific coast of Mexico are used as a second-class fish species for human consumption (Aguilar-Palomino et al., 1996). The dwarf weakfish (Cynoscion nannus) (Castro-Aguirre and Arvizu-Martínez, 1976) is often caught as bycatch in the shrimp fishery but, because of its small size (<27 cm TL, total length), it is not considered a valuable resource. This species can be found in great numbers in waters between 100 and 812 m (Allen and Robertson, 1994; Fischer et al., 1995) associated with the soft-bottom regions off the coast of Jalisco and Colima (González-Sansón et al., 1997).

Quantifying intrapopulation variability in stable isotope data for Spotted Seatrout (Cynoscion nebulosus)

Stable isotope (SI) values of carbon (δ13C) and nitrogen (δ15N) are useful for determining the trophic connectivity between species within an ecosystem, but interpretation of these data involves important assumptions about sources of intrapopulation variability. We compared intrapopulation variability in δ13C and δ15N for an estuarine omnivore, Spotted Seatrout (Cynoscion nebulosus), to test assumptions and assess the utility of SI analysis for delineation of the connectivity of this species with other species in estuarine food webs. Both δ13C and δ15N values showed patterns of enrichment in fish caught from coastal to offshore sites and as a function of fish size. Results for δ13C were consistent in liver and muscle tissue, but liver δ15N showed a negative bias when compared with muscle that increased with absolute δ15N value. Natural variability in both isotopes was 5–10 times higher than that observed in laboratory populations, indicating that environmentally driven intrapopulation variability is detectable particularly after individual bias is removed through sample pooling. These results corroborate the utility of SI analysis for examination of the position of Spotted Seatrout in an estuarine food web. On the basis of these results, we conclude that interpretation of SI data in fishes should account for measurable and ecologically relevant intrapopulation variability for each species and system on a case by case basis.

Growth, mortality, and hatchdate distributions of larval and juvenile spotted seatrout (Cynoscion nebulosus) in Florida Bay, Everglades National Park

Life history aspects of larval and, mainly, juvenile spotted seatrout (Cynoscion nebulosus) were studied in Florida Bay, Everglades National Park, Florida. Collections were made in 1994−97, although the majority of juveniles were collected in 1995. The main objective was to obtain life history data to eventually develop a spatially explicit model and provide baseline data to understand how Everglades restoration plans (i.e. increased freshwater flows) could influence spotted seatrout vital rates. Growth of larvae and juveniles (<80 mm SL) was best described by the equation loge standard length = –1.31 + 1.2162 (loge age). Growth in length of juveniles (12–80 mm SL) was best described by the equation standard length = –7.50 + 0.8417 (age). Growth in wet weight of juveniles (15–69 mm SL) was best described by the equation loge wet-weight = –4.44 + 0.0748 (age). There were no significant differences in juvenile growth in length of spotted seatrout in 1995 between three geographical subdivisions of Florida Bay: central, western, and waters adjacent to the Gulf of Mexico. We found a significant difference in wet-weight for one of six cohorts categorized by month of hatchdate in 1995, and a significant difference in length for another cohort. Juveniles (i.e. survivors) used to calculate weekly hatchdate distributions during 1995 had estimated spawning times that were cyclical and protracted, and there was no correlation between spawning and moon phase. Temperature influenced otolith increment widths during certain growth periods in 1995. There was no evidence of a relationship between otolith growth rate and temperature for the first 21 increments. For increments 22–60, otolith growth rates decreased with increasing age and the extent of the decrease depended strongly in a quadratic fashion on the temperature to which the fish was exposed. For temperatures at the lower and higher range, increment growth rates were highest. We suggest that this quadratic relationship might be influenced by an environmental factor other than temperature. There was insufficient information to obtain reliable inferences on the relationship of increment growth rate to salinity.