Diversity of estuarine movements of striped bass (Morone saxatilis): a synoptic examination of an estuarine system in southern New Jersey

We determined the dis-tribution of multiple (n=68; 508−978 mm total length [TL]) striped bass (Morone saxatilis) along the estua-rine salinity gradient in the Mullica River−Great Bay in southern New Jersey over two years to determine the diversity of habitat use and the movements of striped bass. Ultrasoni-cally tagged fish were detected in this estuarine area by means of wireless hydrophones deployed at four gates inside the entrance of the study area and farther up to tidal freshwater (38 km). Numerous individuals frequently departed and returned to the estuary, primarily in the spring and late fall over periods of 15−731 days at liberty. The period of residency and degree of movement of individuals to and from the estuary varied extensively among seasons and years. The diversity of movements in and out of, as well as within, the estuary differed from the less-complex patterns reported in earlier studies, perhaps because of the comprehensive and synoptic nature of this study.

Reproductive biology, spawning season, and growth of female rex sole (Glyptocephalus zachirus) in the Gulf of Alaska

Rex sole (Glyptocephalus zachirus) have a wide distribution throughout the North Pacific, ranging from central Baja California to the western Bering Sea. Although rex sole are an important species in the commercial trawl fisheries off the U.S. West Coast, knowledge of their reproductive biology is limited to one study off the Oregon coast where ovaries were analyzed with gross anatomical methods. This study was initiated to determine reproductive and growth parameters specific to rex sole in the Gulf of Alaska (GOA) stock. Female rex sole (n=594) ranging in total length from 166 to 552 mm were collected opportunistically around Kodiak Island, Alaska, from February 2000 to October 2001. All ovaries were analyzed by using standard histological criteria to determine the maturity stage. Year-round sampling of rex sole ovaries confirmed that rex sole are batch spawners and have a protracted spawning season in the GOA that lasts at least eight months, from October to May; the duration of the spawning season and the months of spawning activity are different from those previously estimated. Female rex sole in the GOA had an estimated length at 50% maturity (ML50) of 352 mm, which is greater than the previously estimated ML50 at southern latitudes. The maximum age of collected female rex sole was 29 years, and the estimated age at 50% maturity (MA50) in the GOA was 5.1 years. The von Bertalanffy growth model for rex sole in the GOA was significantly different from the previously estimated model for rex sole off the Oregon coast. This study indicated that there are higher growth rates for rex sole in the GOA than off the Oregon coast and that there are differences in length at maturity and similarity in age at maturity between the two regions.

Hatching date, nursery grounds, and early growth of juvenile walleye pollock (Theragra chalcogramma) off northern Japan*

Walleye pollock (Theragra chalcogramma) is widely distributed in the North Pacific Ocean and plays an important role in coastal subarctic ecosystems. The Japanese Pacific population of this species is one of the most important demersal fishes for commercial fisheries in northern Japan. The population is distributed along the Pacific coast of Hokkaido and the Tohoku area (Fig. 1), which is the southern limit of distribution of the species in the western North Pacific. In Funka Bay, the main spawning ground for this population, pollock spawn from December to March (Kendall and Nakatani, 1992). Planktonic eggs and larvae are transported into the bay, where juveniles usually remain until late July when they reach 60−85 mm in total length (Hayashi et al., 1968; Nakatani and Maeda, 1987). These juvenile pollock then migrate from Funka Bay eastward to the Doto area off southeastern Hokkaido (Honda et al., 2004). Many studies on eggs, larvae, and juveniles of the species have been conducted in or near Funka Bay, but little information is available on the ecology of the early life stages in the Tohoku area. Hashimoto and Ishito (1991) suggested that eggs are transported from Funka Bay southward to the Tohoku area by the coastal branch of the Oyashio Current, but there has been no study to verify this hypothesis.

Sexual differentiation and gonad development in striped mullet (Mugil cephalus L.) from South Carolina estuaries*

This study examined the sexual differentiation and reproductive dynamics of striped mullet (Mugil cephalus L.) in the estuaries of South Carolina. A total of 16,464 specimens were captured during the study and histological examination of sex and maturity was performed on a subsample of 3670 fish. Striped mullet were sexually undifferentiated for the first 12 months, began differentiation at 13 months, and were 90% fully differentiated by 15 to 19 months of age and 225 mm total length (TL). The defining morphological characteristics for differentiating males was the elongation of the protogonial germ tissue in a corradiating pattern towards the center of the lobe, the development of primary and secondary ducts, and the lack of any recognizable ovarian wall structure. The defining female characteristics were the formation of protogonial germ tissue into spherical germ cell nests, separation of a tissue layer from the outer epithelial layer of the lobe-forming ovarian walls, a tissue bud growing from the suspensory tissue that helped form the ovary wall, and the proliferation of oogonia and oocytes. Sexual maturation in male striped mullet first occurred at 1 year and 248 mm TL and 100% maturity occurred at age 2 and 300 mm TL. Female striped mullet first matured at 2 years and 291 mm total length and 100% maturity occurred at 400 mm TL and age 4. Because of the open ocean spawning behavior of striped mullet, all stages of maturity were observed in males and females except for functionally mature females with hydrated oocytes. The spawning season for striped mullet recruiting to South Carolina estuaries lasts from October to April; the majority of spawning activity, however, occurs from November to January. Ovarian atresia was observed to have four distinct phases. This study presents morpholog ical analysis of reproductive ontogeny in relation to size and age in South Carolina striped mullet. Because of the length of the undifferentiated gonad stage in juvenile striped mullet, previous studies have proposed the possibility of protandric hermaphrodism in this species. The results of our study indicate that striped mullet are gonochoristic but capable of exhibiting nonfunctional hermaphroditic characteristics in differentiated mature gonads.

Some reproductive aspects of Chrysichthys nigrodigitatus (Lacépède) from Cross River, Nigeria

Between May and October 1990, fecundity, egg size and condition factor of Chrysichthys nigrodigitatus (Lacépède) in the Cross River, Nigeria, were studied. The fecundity (F) of this population varied from 3 046 eggs (total length, L=28.5 cm) to 28 086 eggs (L=64 cm). A mean relative fecundity of 231 eggs/cm or 13 eggs/g of fish was obtained for this population. The fecundity of this population can be estimated with the formula F=2.511 · L 2.30 or F=52.893 · W 0.78 , total length being in cm and weight (W) in g. The mean egg diameter of this population varied from 0.65 mm to 3.54 mm. Condition factor (CF) of the population varied from 0.24 to 1.34 with 0.977 as the mean; 52.8% had CF higher than the mean and 47% had CF above unity. Smaller fish in this population were in better condition than bigger ones. The egg size and condition factor obtained in this study are evidence that the Cross River population of C. nigrodigitatus can provide excellent broodstock.

On the growth, mortality and recruitment of the spiny lobster (Panulirus homarus) in Sri Lankan waters

Monthly length-frequency data of spiny lobster Panulirus homarus collected from the south coast of Sri Lanka during 1988-1990 were analyzed to estimate von Bertallanfy growth parameters. The asymptotic lengths estimated using Wetherall plots were 322 mm and 315 mm total length for the males and females, respectively. Using o' values of 3.53 for males and 3.61 for females, the growth constant (K) was estimated as 0.21 year super(1) and 0.27 year super(1) for the males and females, respectively. The estimates of natural and total mortality (M and Z) are 0.98 year super(1), 1.96 year super(1) for males and 0.92 year super(1), 1.54 year super(1) for females respectively. Recruitment appears to occur in two pulses per year.

Growth and emigration of white shimp, Litopenaeus vannamei, in the Mar Muerto Lagoon, Southern Mexico

Microcohorts of white shrimp, Litopenaeus vannamei, were sampled with a cast net at fortnightly intervals in the Mar Muerto Lagoon, Southern Mexico. Shrimp recruited to the lagoon throughout the sampling period (January to August 1993). Mean growth rates of microcohorts ranged from 0.21 to 1.21 mm total length (TL) per day. Juvenile shrimp mainly between the sizes of 70 to 80 mm TL emigrated from the lagoon. Growth and the onset of emigration appeared to be related to water salinity.

Observations on gillnet catches of Kariba tilapia, Oreochromis mortimeri from Bumi Basin of Lake Kariba, Zimbabwe

Gillnet catches of Oreochromis mortimeri (Trewavas) were studied in the Bumi Basin of Lake Kariba in 1988 and 1989. Total length (TL) was positively correlated with standard length (SL). The linear relationship between TL and SL was TL=1.91 + 1.22 SL (r super(2)=0.982). The relationship between SL and weight in g (W) was of the form W = 0.12 SL super(2.67). Maximum standard length (L sub(max)) was 33 cm and asymptotic length (L sub( infinity )) was 34.7 cm. Monthly ratios of male to female varied between 0.6:1 and 13:1. The mean ratio was 57.4% male: 42.6%female. Monthly condition factors varied between 3.19 and 5.11 in males, and between 3.18 and 5.14 in females. Catches were higher in 1989 compared to 1988 and possible reasons for these differences are discussed.

Age, growth, mortality, and radiometric age validation of gray snapper (Lutjanus griseus) from Louisiana

The gray snapper (Lutjanus griseus) is a temperate and tropical reef fish that is found along the Gulf of Mexico and Atlantic coasts of the southeastern United States. The recreational fishery for gray snapper has developed rapidly in south Louisiana with the advent of harvest and seasonal restrictions on the established red snapper (L. campechanus) fishery. We examined the age and growth of gray snapper in Louisiana with the use of cross-sectioned sagittae. A total of 833 specimens, (441 males, 387 females, and 5 of unknown sex) were opportunistically sampled from the recreational fishery from August 1998 to August 2002. Males ranged in size from 222 to 732 mm total length (TL) and from 280 g to 5700 g total weight (TW) and females ranged from 254 to 756 mm TL and from 340 g to 5800 g TW. Both edge analysis and bomb radiocarbon analyses were used to validate otolith-based age estimates. Ages were estimated for 718 individuals; both males and females ranged from 1 to 28 years. The von Bertalanffy growth models derived from TL at age were Lt = 655.4{1–e[–0.23(t)]} for males, Lt = 657.3{1–e[– 0.21(t)]} for females, and L t = 656.4{1–e[– 0.22 (t)]} for all specimens of known sex. Catch curves were used to produce a total mortality (Z) estimate of 0.17. Estimates of M calculated with various methods ranged from 0.15 to 0.50; however we felt that M= 0.15 was the most appropriate estimate based on our estimate of Z. Full recruitment to the gray snapper recreational fishery began at age 4, was completed by age 8, and there was no discernible peak in the catch curve dome.

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).

An assessment of scup (Stenotomus chrysops) and black sea bass (Centropristas striata) discards in the directed otter trawl fisheries in the Mid-Atlantic Bight

This study was undertaken to re-assess the level of scup (Stenotomus chrysops) discards by weight and to evaluate the effect of various codend mesh sizes on the level of scup discards in the winter-trawl scup fishery. Scup discards were high in directed scup tows regardless of codend mesh — typically one to five times the weight of landings. The weight of scup discards in the present study did not differ significantly from that recorded in scup-targeted tows in the NMFS observer database. Most discards were required as such by the 22.86 cm TL (total length) fish-size limit for catches. Mesh sizes ≤12.7 cm, including the current legal mesh size (11.43 cm) did not adequately filter out scup smaller than 22.86 cm. The median length of scup discards was about 19.83 cm TL. Lowering the legal size for scup from 22.86 to 19.83 cm TL would greatly reduce discard mortality. Scup discards were a small fraction (0.4%) of black sea bass (Centropristis striata) landings in blacksea-bass−targeted tows. The black sea bass fishery is currently regulated under the small-mesh fishery gearrestricted area plan in which fishing is prohibited in some areas to reduce scup mortality. Our study found no evidence to support the efficacy of this management approach. The expectations that discarding would increase disproportionately as the trip limit (limit [in kilograms] on catch for a species) was reached towards the end of the trip and that discards would increase when the trip limit was reduced from 4536 kg to 454 kg at the end of the directed fishing season were not supported. Trip limits did not significantly affect discard mortality.

Age and growth estimates of the thorny skate (Amblyraja radiata) in the western Gulf of Maine

The northwest Atlantic population of thorny skates (Amblyraja radiata) inhabits an area that ranges from Greenland and Hudson Bay, Canada, to South Carolina. Despite such a wide range, very little is known about most aspects of the biology of this species. Recent stock assessment studies in the northeast United States indicate that the biomass of the thorny skate is below the threshold levels mandated by the Sustainable Fisheries Act. In order to gain insight into the life history of this skate, we estimated age and growth for thorny skates, using vertebral band counts from 224 individuals ranging in size from 29 to 105 cm total length (TL). Age bias plots and the coefficient of variation indicated that our aging method represents a nonbiased and precise approach for the age assessment of A. radiata. Marginal increments were significantly different between months (Kruskal-Wallis P<0.001); a distinct trend of increasing monthly increment growth began in August. Age-at-length data were used to determine the von Bertalanffy growth parameters for this population: L∞ = 127 cm (TL) and k= 0.11 for males; L∞ = 120 cm (TL) and k= 0.13 for females. The oldest age estimates obtained for the thorny skate were 16 years for both males and females, which corresponded to total lengths of 103 cm and 105 cm, respectively.

Territorialidade e ecologia reprodutiva de Formicivora littoralis (Thamnophilidae) na Restinga da Massambaba, RJ

A distribuição espacial dos indivíduos é decorrente da presença e ausência de microhábitats adequados, sendo aqueles que se estabelecem nas melhores manchas favorecidos pela seleção natural. A aquisição de um território permite a manutenção do indivíduo e o sucesso reprodutivo. A reprodução é considerada de alto custo energético, pois há deslocamento dos recursos para a manutenção de uma prole em vez de serem incorporados no crescimento individual. Investir em uma prole não significa alcançar o sucesso reprodutivo. O sucesso reprodutivo pode ser afetado, por exemplo, por eventos de predação, disponibilidade de alimento e cuidado parental. Este último pode ser realizado por ambos os membros do par reprodutor ou por apenas um deles. A deserção do cuidado parental por um dos sexos pode ser uma resposta à cópulas extra-par. Formicivora littoralis tem distribuição muito restrita. É a única espécie de ave considerada endêmica de restinga e se encontra ameaçada de extinção, embora seja localmente abundante. O presente estudo teve como objetivos: 1) estimar os tamanhos de territórios e compara-los entre estação reprodutiva e não reprodutiva; 2) testar a influência do tamanho dos indivíduos e quantidade de vizinhos no tamanho do território; 3) descrever ninhos, ovos, filhotes e determinar o sucesso reprodutivo; 4) quantificar o cuidado parental; 5) desenvolver marcadores moleculares de microssatélites para determinar paternidade. Para os indivíduos capturados e marcados individualmente, foram obtidas amostras de sangue e medidas morfométricas (tarso, asa, cauda, comprimento total), além do peso. Os tamanhos dos territórios foram estimados pelo método do mínimo polígono convexo (unindo pontos onde machos foram registrados vocalizando). A densidade foi estimada com base no tamanho dos territórios. Aspectos da reprodução foram acessados por meio de busca mensal por ninhos e acompanhamento destes por dois dias consecutivos. Foram obtidas as taxas de predação e a quantificação do cuidado parental. Para a paternidade foram utilizados sete marcadores de microssatélites, desenvolvidos para este fim. Formicivora littoralis possui território pequeno (0,008 a 0,32ha), que varia de acordo com a estação (menor na estação reprodutiva). O tamanho do território não foi relacionado com o tamanho do indivíduo, mas apresentou resultado significativo quando comparado com a quantidade de territórios vizinhos, mostrando ser menor quanto maior o número de vizinhos. A espécie apresentou elevada densidade (0,53 a 1,15 indivíduos/km2). Com relação à reprodução, ninhos tem o formato de cesto aberto onde foram postos no máximo dois ovos. Os filhotes nasceram sem penas. A razão sexual no ninho foi igual em ambos os sexos. A taxa de predação foi elevada na fase de incubação quando comparada à fase no ninho após a eclosão. O cuidado parental (durante a incubação e com os filhotes) foi realizado pelos dois sexos, sem diferenças na proporção do investimento realizado. Dos nove ninhos analisados, todos contiveram pelo menos um ninhego proveniente de fertilização extra-par. Um total de 81,2% dos ninhegos (13 em 16) não foram prole biológica do macho do par reprodutor que realizava o cuidado parental e que se encontrava pareado socialmente com a fêmea. Essa taxa foi a mais elevada entre os estudos já realizados nos neotrópicos

First Record of the Ragged-tooth Shark, Odontaspis ferox, off the U.S. Atlantic Coast

On 11 September 1994, a large shark was captured and later identified as the ragged-tooth shark, Odontaspis ferox (Risso). The shark was captured during routine bottom trawl survey operations onboard the NOAA R/V Albatross IV, approximately 25 n.mi. south-southeast of Cape Hatteras, N.C. (lat. 34° 51' N, long. 75° 26' W) with a “36 Yankee” bottom trawl towed at 3.5 knots. Average water depth at the time of capture was 173 m, bottom temperature was 17.8°C, and salinity was 36.41‰. Total length (cm), fork length (cm), weight (kg), and sex were recorded, the specimen was tagged, photographed, and returned live to t

Seasonal Occurrence of the White Shark, Carcharodon carcharias, in Waters off the Florida West Coast, with Notes on its Life History

The white shark, Carcharodon carcharias, is considered rare in the Gulf of Mexico; however, recent longline captures coupled with historical landings information suggest that the species occurs seasonally (winter-spring) within this region. We examined a total of seven adult and juvenile white sharks (185-472 em total length) captured in waters off the west coast of Florida. Commercial longline fisheries were monitored for white sharks during all months (1981-94), but this species was captured only from January to April. All white sharks were captured in continental shelf waters from 37 to 222 km off the west coast of Florida when sea surface temperatures ranged from 18.7° to 21.6°C. Depths at capture locations ranged from 20 to 164 m. Fishing gear typically used in Gulf of Mexico offshore fisheries may not be effective at capturing this species, and the apparent rarity of white sharks in this area may be, in part, a function of gear bias.