Abstract:This study aimed to describe the gonadal histology and the reproductive cycle of Crassostrea brasiliana in the mangroves of Guaratuba Bay in southern Brazil. Adults were collected monthly from January 2010 to April 2011 from three sampling sites in intertidal oyster beds. The animals were evaluated using biometric and histological analyses of the gonads. The gonadal tissue samples were processed according to the standard histological procedures, and permanent slides were prepared using Harris' haematoxylin and… Show more
“…This constant reproductive pattern has also been found in other Crassostrea spp., in subtropical and tropical areas, showing significant differences to the pattern of oysters in temperate regions. (Baqueiro‐Cárdenas et al, ; Castilho‐Westphal et al, ; Lenz & Boehs, ; Vaschenko, Hsieh, & Radashevsky, ). The reproductive period of mollusks living in temperate and cold climates is seasonal, the frequency of reproductive activity increases as latitude decreases (Baqueiro, ).…”
Section: Discussionmentioning
confidence: 99%
“…The allometrics may be related to the changes in organizational structure. During gonadal development, small acini interspersed with a large quantity of storage connective tissue develop into large and juxtaposed acini without interstitial tissue (Castilho‐Westphal et al, ). In this process, the varieties of tissue structure and biochemical compositions may lead to the change of metal accumulation rate.…”
Section: Discussionmentioning
confidence: 99%
“…However, there are other patterns in the gonadal development of oysters. Oysters living in some subtropical and tropical sea areas reproduce constantly; there are multiple reproductive cycles per year, gametogenesis is fast, the spawning extended and gonads recover quickly after spawning; all gonadal development stages are present throughout the year in one population (Baqueiro‐Cárdenas, Aldana‐Aranda, Sevilla, & Rodríguez‐Espinosa, ; Castilho‐Westphal, Magnani, & Ostrensky, ; George‐Zamora, Sevilla‐Hernández, & Aldana‐Aranda, ). These can cause significant differences in the stages of gonadal development of individual oysters collected at the same time.…”
Metal enrichment makes oyster considered to be an appropriate food source for trace elements, but excessive accumulation can threaten human health. Reproduction is an important biotic factor that affects the metal accumulation in oysters. However, the influence of continuous gonad development model on metal accumulation in some subtropical oysters is still unclear. The present study addresses the concentrations of trace metals and glycogen associated with the gonadal and somatic tissues throughout the reproductive cycle of diploid and triploid Crassostrea angulata cultured in Fujian, China. Cu, Zn and Pb contents of gonads were negatively correlated (p < 0.05) with gonadosomatic index (GSI). The correlation between Cd content and GSI was not significant. There was a positive correlation (p < 0.05) between GSI and Mn content in female gonads while the correlation was negative (p < 0.05) in males, indicating Mn plays an important role in gametogenesis of females. The effects of gonadal maturity and gender on metal accumulation in somatic tissue were not significant (p > 0.05). The concentrations of all metals in sterile triploids were not significantly different from those of the somatic tissue of diploids. Gonadal glycogen content showed a negative correlation with the GSI. However, somatic glycogen content was not affected by gonadal development, indicating that the energy consumed during gametogenesis comes mainly from recently ingested food rather than from energy stored in somatic tissue. The effects of the gonadal development on the metal accumulation in oysters varied according to the metal and tissue type.
“…This constant reproductive pattern has also been found in other Crassostrea spp., in subtropical and tropical areas, showing significant differences to the pattern of oysters in temperate regions. (Baqueiro‐Cárdenas et al, ; Castilho‐Westphal et al, ; Lenz & Boehs, ; Vaschenko, Hsieh, & Radashevsky, ). The reproductive period of mollusks living in temperate and cold climates is seasonal, the frequency of reproductive activity increases as latitude decreases (Baqueiro, ).…”
Section: Discussionmentioning
confidence: 99%
“…The allometrics may be related to the changes in organizational structure. During gonadal development, small acini interspersed with a large quantity of storage connective tissue develop into large and juxtaposed acini without interstitial tissue (Castilho‐Westphal et al, ). In this process, the varieties of tissue structure and biochemical compositions may lead to the change of metal accumulation rate.…”
Section: Discussionmentioning
confidence: 99%
“…However, there are other patterns in the gonadal development of oysters. Oysters living in some subtropical and tropical sea areas reproduce constantly; there are multiple reproductive cycles per year, gametogenesis is fast, the spawning extended and gonads recover quickly after spawning; all gonadal development stages are present throughout the year in one population (Baqueiro‐Cárdenas, Aldana‐Aranda, Sevilla, & Rodríguez‐Espinosa, ; Castilho‐Westphal, Magnani, & Ostrensky, ; George‐Zamora, Sevilla‐Hernández, & Aldana‐Aranda, ). These can cause significant differences in the stages of gonadal development of individual oysters collected at the same time.…”
Metal enrichment makes oyster considered to be an appropriate food source for trace elements, but excessive accumulation can threaten human health. Reproduction is an important biotic factor that affects the metal accumulation in oysters. However, the influence of continuous gonad development model on metal accumulation in some subtropical oysters is still unclear. The present study addresses the concentrations of trace metals and glycogen associated with the gonadal and somatic tissues throughout the reproductive cycle of diploid and triploid Crassostrea angulata cultured in Fujian, China. Cu, Zn and Pb contents of gonads were negatively correlated (p < 0.05) with gonadosomatic index (GSI). The correlation between Cd content and GSI was not significant. There was a positive correlation (p < 0.05) between GSI and Mn content in female gonads while the correlation was negative (p < 0.05) in males, indicating Mn plays an important role in gametogenesis of females. The effects of gonadal maturity and gender on metal accumulation in somatic tissue were not significant (p > 0.05). The concentrations of all metals in sterile triploids were not significantly different from those of the somatic tissue of diploids. Gonadal glycogen content showed a negative correlation with the GSI. However, somatic glycogen content was not affected by gonadal development, indicating that the energy consumed during gametogenesis comes mainly from recently ingested food rather than from energy stored in somatic tissue. The effects of the gonadal development on the metal accumulation in oysters varied according to the metal and tissue type.
“…In his study of gonadal development in bivalve molluscs, Lubet () was one of the first to propose a gametogenic scale for Mytilus edulis (Linnaeus, 1758). There are now various reproductive classifications for various species, which are based on qualitative (Berthelin et al., ; Castilho‐Westphal, Magnani, & Ostrensky, ; Dinamani, ; Steele & Mulcahy, ) and quantitative criteria (Bodoy, Prou, & Berthome, ; Delgado & Pérez Camacho, ; Lango‐Reynoso, Chávez‐Villalba, Cochard, & Le Pennec, ).…”
The oyster Crassostrea gigas was introduced in Spain for aquaculture purposes; however, until now, it is not known whether populations are established in the wild, being necessary to define whether this species is spawning and which environmental variables trigger this process. The influence of environmental parameters on the reproduction of C. gigas was evaluated from January 2008 to October 2009 with oysters grown on a raft in the Ría de Arousa (Galicia, NW Spain). Temperature and chlorophyll a are directly correlated to sexual maturation. Oysters can mature at temperatures below 14°C. The temperature necessary for spawning differs between the sexes, requiring a temperature above 15°C for males and 18°C for females.Females had a single massive spawn between June and September, while males had partial spawning from May to December with two peaks, one in May-September and another in October-December, with the second peak more pronounced. The first spawning peak is related to high temperatures and concentrations of chlorophyll a, and the second spawning peak is mainly related to the food availability in the water.The spawning asynchrony may be impeding establishment of wild C. gigas populations in Spain.
K E Y W O R D Schlorophyll a, mollusc, reproductive biology, spawning, temperature
“…However, such small-scale units, largely aided by government incentives, have greatly contributed to the dissemination of native mangrove oyster culture along the Brazilian coast (Pereira & Rocha 2012). Crassostrea gasar has been cultivated on a small-scale in south-eastern and southern Brazil for some time now (Muniz et al 1986;Absher et al 2000;Christo & Absher 2006), and there has been a recent surge in research on its culture, especially in Santa Catarina and Paran a (Silveira et al 2011;Lopes et al 2013;Ramos et al 2013Ramos et al , 2014Gomes et al 2014;Tureck et al 2014;Castilho-Westphal et al 2015;Silva et al 2015). Yet, overall production of the mangrove oyster C. gasar remains low, perpetuating the asymmetry in Brazilian oyster production.…”
Oyster culture activity along the eastern Amazon mangrove coast in Pará state, Brazil, was evaluated using socio‐economic data to support its management and future development. Between 2013 and 2014, surveys were carried out in the region's seven oyster culture associations through interviews with the president of each association as well as with 56 members (72% of the total). Further data up to 2016 were obtained from annual reports of the Serviço Brasileiro de Apoio às Micro e Pequenas Empresas in Pará and the Instituto Brasileiro de Geografia e Estatística. Two associations stand out from the rest due to their larger on‐growing areas and total production in 2013. However, smaller associations are more efficient with higher production per unit area. Currently, oyster culture in Pará provides an alternative source of income for 80 families, where total production has increased from 8.25 tons in 2013 to 41.8 tons in 2016. Although associations have grown in number since 2006, along with increased capacity and production due to government assistance, in comparison with other regions of Brazil, they need to be better organized internally, including regular monitoring of growth, production and environmental variables, development of depuration facilities and improved distribution and presentation of products. Diversification of seed supply among different locations is desirable. There should also be less dependence on public funding and more partnerships with private enterprise, as well as active coparticipation in the development of legislation and public policies regulating both oyster culture and protection of natural oyster beds.
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