Density and reproduction of the Queen Conch Eustrombus gigas (Mesogastropoda: Strombidae) at Cabo Cruz, Desembarco del Granma National Park, Cuba Densidad y reproducción de la concha reina Eustrombus gigas (Mesogastropoda: Strombidae) en Cabo Cruz, Parque Nacional Desembarco del Granma, Cuba
Yuself R. Cala1*, Alberto de Jesús-Navarrete2*, Frank A. Ocaña3* & José Oliva-Rivera2
The queen conch Eustrombus gigas is an important fisheries resource in the Caribbean region. In Cuba Island the studies about this resource are very scarce and particularly in the Southeastern regions of the country. With the aim to get important fishery information about this gastropod, adult Queen Conch density and frequency of reproductive activity were evaluated in Cabo Cruz, Cuba, during 2009-2010. Data from three seasons were obtained (rainy, dry and cold fronts periods) from three different areas: Farito, Guafe and Laguna. The highest density was observed in cold fronts season (468.5ind./ha) and the lowest occurred during the dry season (268.5ind./ha). The highest density was reported at Laguna (520.4ind./ha) and the lowest at Farito (290.9ind./ha). In total, 158 reproductive events were observed. The highest frequency was reported in rainy season (36%), followed by dry (9%) and cold fronts (5%) seasons. Reproductive behavior (mating and egg laying) was related to temperature and photoperiod. Reproductive activity was observed during the whole year, which suggests the existence of an important Queen Conch reserve in the Southeastern region of Cuba and an apparently self-sufficient population for recruitment. From our results we may conclude that, the population’s sustainable exploitation is viable if the following management measures are observed: functional zoning within the area, rotation of fishing areas and a closed season. We recommend that the Laguna site should be protected as a reproduction zone and banned for fishing activities.
El Eustrombus gigas es un recurso pesquero importante en la región del Caribe. En Cuba, los estudios acerca de este recurso son muy escasos y en la zona Sur-oriental del país son casi nulos. En este trabajo se evalúa la densidad de adultos y frecuencia de la evidencia reproductiva de Eustrombus gigas Linneus 1758 en Cabo Cruz, Cuba, en el periodo 2009-2010. Se obtuvieron datos de tres períodos (lluvias, seca y frentes fríos) en tres zonas: Farito, Guafe y Laguna. La mayor densidad de adultos se observó en frentes fríos (468.5ind./ha) y la menor en seca (268.5ind./ ha). Por zonas, la mayor densidad de adultos se reportó en Laguna (520.4ind./ha) y la menor en Farito (290.9ind./ha). Se observaron 158 evidencias reproductivas. La mayor frecuencia se reportó en lluvias (36%). La temperatura se relacionó con la frecuencia de desove y cantidad de masas de huevos, y el fotoperiodo con la cantidad de agregaciones y frecuencia de cópula. Se observó actividad reproductiva intensa durante todo el año, lo que sugiere una importante reserva de la especie en la región sur-oriental de Cuba y una aparente autosuficiencia de la población para el reclutamiento. La explotación sostenible de la población es viable y Laguna debe ser protegida como zona de reproducción.
Palabras clave: Mar Caribe, reproducción, manejo pesquero, áreas protegidas, Eustrombus gigas.
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The queen conch Eustrombus gigas (Linnaeus 1758), formerly known as Strombus gigas (Petuch 2004, Petuch & Roberts 2007), is one of the most valuable coastal resources in the Caribbean region (de Jesús-Navarrete & Oliva- Rivera 1997, Theile 2001, Brito-Manzano et al. 2006). This large mollusk has a high aesthetic and ecological value throughout the Caribbean Sea and surrounding areas from Southern Florida in ]]>
1974). The species is one of the most important coastal resources for the region and is second in importance after the spiny lobster (Panulirus argus Latreille 1804) (Appeldoorn 1994a, de Jesús-Navarrete & Oliva-Rivera 1997).
At the regional level in the ]]>
et al. 1992, 1996) and in the Red List of Threatened Animals of the International Union for Conservation of Nature-IUCN 1994-as a ‘commercially threatened’ species (Gómez-Campos et al. 2010). ]]>
This situation has led to a variety of management measures including the total fisheries closure, closed seasons, catch quotas, and minimum sizes for harvest (Appeldoorn 1994a), as well as the development of its culture as an alternative use and ecological restoration of damaged populations (Davis 2000). Marine protected areas have been established in many countries to protect wild populations (Appeldoorn 1994b, Stoner 1997). ]]>
There are many studies of this species in the Caribbean region (Randall 1964, Appeldoorn 1990, Glazer & Berg 1992, Stoner et al. 1996, Basurto et al. 2005, Jared et al. 2006, Ávila-Poveda & Baqueiro-Cárdenas 2006, Gómez-Campos et al. ]]>
et al. 2012a), but few have been conducted in Cuba. For the Eastern coast of Cuba, Alcolado (1976) studied the growth, morphological variations of the shell and other biological data. Some commercial fishing assessments were made by Formoso (2001) and Álvarez-Lemus & Formoso (2005). Recently, Cala (2006) addressed socio-environmental problems associated with this resource, the conflicts of use and impacts over the distribution area of E. gigas at Cabo Cruz. He proposed two strategic guidelines to ]]>
The reproductive evidence studies (aggregations, mating, spawning and presence of egg masses) are scarce for this species. Stoner & Ray (2000) carried out a study in The Bahamas, showing a relationship between conch density and frequency of reproduction. For example, no mating was observed when densities were ]]>
et al. (2012a) found that similar densities were required for mating in two new study sites (47 and 64 adults ind./ha for Berry Islands and Andros Island in the Bahamas, respectively). At Banco Chinchorro, Mexico, de Jesús-Navarrete et al. (2003) reported very low reproductive activity, also related to the adults low density because of overfishing, and indicated the existence of an Allee effect in the population. At Cabo Cruz, Alcolado (1976) reported an average density ]]>
E. gigas in Cuban waters.
This paper presents an analysis of adult density, physical variables and reproductive activity for E. gigas at Cabo Cruz, one of the least studied sites of the Cuban ]]>
E. gigas in the study area. It is also the first of its kind in the Southeastern region of Cuba.
Materials and methods
Study area: Cabo Cruz is located in the Southeastern region of Cuba (19°50’14.1’’ N - 77°44’15.7’’ W) where the protected area Desembarco del Granma National Park occupies 32 576ha. The study area is located on the reef lagoon of Cabo Cruz, in the most Western region of the park. This lagoon is characterized by extensive sandy bottoms with patches of Thalassia testudinum ]]>
Syringodium filiforme (Kützing in Hohenacker). There is also significant abundance of some macroalgae species, mainly of the genera Dictyota, Penicillus and Ceramium (Alcolado 1976). Lagoon depth ranges from 0-6m. ]]>
Surveys were conducted at three different zones into the reef lagoon: Guafe (19°50’828’’ N - 77°44’711’’ W), Farito (19°50’320’’ N - 77°44’581’’ W) and Laguna (19°50’225’’ N - 77°44’188’’ W). In addition, three climatic seasons were analyzed: rainy (May-August), dry (September-December) and cold fronts (January-April, although, these events begin usually after December) (Gónzalez 1999). For this study, we analyzed the cold fronts average in the ]]>
For each zone, the water column salinity (UPS, Mean±SE) was measured using a portable refractometer (RF20 model) and the Practical Salinity scale. A temperature & light data logger HOBO was programmed to take readings every 30min of other abiotic variables such ]]>
Conch sampling: In each study zone three sampling sites were established, each with three transects of 100x2m (400m2). To evaluate conch population density, we measured the perpendicular distance of each conch to the transect line using 1m length PVC pipes. The density was calculated ]]>
et al. 1993). The total density and adult density was determined for each zone and season (ind./ ha, Mean±SE).The conchs were collected at each zone by free diving. The siphonal length (SL) and the lip thickness (LT) were registered with a caliper with a precision of 0.1mm.
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All conchs were classified as juveniles or adults taking the lip thickness as an indicator of sexual maturity. The range of variation in lip thickness measurement that determines the age at sexual maturity and the onset of adult age are highly variable (Gómez-Campo et al. 2010); this can be >1mm as used by Perez-Perez & Aldana-Aranda (2000) to 14.2mm as used by Appeldoorn (1988). For this study, we took into account the presence of an extended lip and the conchs withlip thickness <8.0mm were ]]>
et al. 2012b).
The absolute frequency of the following reproductive events was recorded at each transect as follows: a) copulation: penis into the female canal, b) spawning: females laying egg mass, c) aggregation: conch group (more than five individuals) and d) egg masses: solitary egg masses (Pérez-Pérez & ]]>
To compare the adult density among zones and seasons, a two-way analysis of variance (ANOVA) was used. Values of salinity and temperature were compared both spatially and temporally with one-way ANOVA. In order to fulfill homoscedasticity requirements, all data were transformed to log (x+1). ANOVA was followed by multiple range tests to achieve
post hoc comparisons.
Pearson correlation analysis was used to evaluate the possible relationship between reproductive activities. To evaluate the relationship between reproductive activities with abiotic variables, a multiple linear regression analysis was performed; prior this analysis, a Pearson correlation test was accomplished to avoid the use of auto-correlated independent variables (abiotic variables) in the model. The model was ]]>
Results
The average water temperature was lowest in the dry season in December (26±0.44°C) and highest in the rainy season in August (28.8±0.05°C) (Fig. 1), statistically significant differences among monthly temperatures were found (ANOVA, p<0.05).Salinity had minimum values in January (32.4±0.4UPS) and maximum in October ]]>
Fig. 1). No significant differences were detected in salinity either among zones or between season (ANOVA, p<0.05).
The photoperiod varied among the study months, with minimum values in November (10.07±0.4hr) in dry season and maximum values in July (12.73±0.1hr) during the rainy season (Fig. 2). ]]>
Light intensity filtered through the water column showed the lowest value in November during the dry season (12.89±2.8lum/ft²) and maximum (97.24±6.5lum/ft²) in the cold front season (January) (Fig. 2). Significant differences were detected in light intensity among months and climatic seasons (ANOVA, p<0.05). A multiple range test confirmed differences among the three seasons.
Density considering the whole population by zone and season at the study area showed higher values at Farito during the dry season (1 767±213.68ind./ha) and lower (247±30.4ind./ha) at Guafe during the rainy season. No significant differences were detected among seasons (ANOVA, p>0.05). Spatial analysis showed that higher density occurred at Farito (1 723±19.2ind./ha) and lower at Guafe (511±22.3ind./ha). No significant differences were detected among zones (ANOVA, p>0.05).
Density of adult individuals showed values ranging from 124.96±9.7ind./ha at Farito in dry season to 674.07±122.3ind./ha at Laguna during the cold fronts season. The highest density for season was observed in cold fronts season (468.5±53.3ind./ha) and lowest in the dry season (268.5±24.5ind./ha). For the study zone, the adults highest density was observed at Laguna (520.4±10.1ind./ha) and lowest at Farito (290.9±19.2ind./ha) (Fig. 3). There were no significant differences either between areas or between seasons in the adult’s density (ANOVA, p>0.05).
During the whole three seasons we observed 158 reproductive events. The highest frequency of reproductive events was observed in the rainy season (36%), followed by dry (9%) and cold front (5%) (Fig. 4A). Spatially, a total of 73 adult aggregations of more than five individuals were reported, distributed at the study zone during the three seasons, although they were observed much more often at Laguna and Farito (6% and 10%, respectively) (Fig. 4B). Copulation was observed on 25 occasions. ]]>
Only one copulation was observed at Guafe during the study (0.3%) and other three copulation were observed at Farito (1.2%); however, this reproductive evidence was more frequent at Laguna (3.7%). It is important to note that Laguna was the only site where we observed spawning activities (2.5%) and 42 egg masses (7.5%). The rest of the egg masses were observed at Farito (1.2%) and Guafe (0.3%).
We found a significant correlation between the frequency of spawning and mating at the study area (r=0.84, p=0.0012, n=81) and between the copulation frequency and the absolute number of egg masses (r=0.73, p=0.0161, n=81). The rest of the reproductive evidence did not show correlations (Pearson, p>0.05) (Table 1).
The absolute frequency of aggregations was positively correlated with photoperiod (r=0.39, p<0.05), just as occurred with the frequency of mating (r=0.40, p<0.05), likewise, the temperature was positively correlated with the number of egg masses (r=0.52, p<0.05) and spawning frequency (r=0.35, p<0.05). The multiple regression models explained significantly 23% of the variance of the aggregation frequency and 12% in the copulation frequency, including the photoperiod as predictor variable that affect both aggregations frequency and copulation frequency directly. Similarly, the multiple regression models explained significantly the 24% of the variance in the number of egg masses and 12% in spawning frequency, including in both cases the temperature as a predictor variable (Table 2).
Discussion
Important variations in density have been reported, both in populations of E. gigas subjected to exploitation by fisheries, as in those located in non-take areas and have been attributed primarily to fluctuations in the environmental conditions, biological interactions and the fishing pressure (Weil & Laughling 1984, Gómez-Campos et al. 2005). In other cases, changes have been associated with variations in recruitment (Roughgarden et al. 1988, de Jesús-Navarrete et al. 2003). Mean density considering the whole population at the study area was higher (1 108±207ind./ha) than other areas of the Caribbean. In despite that statistical analysis showed no significantly differences in density among zones, the adult density at Laguna represented up to 52% of the total density of the study area indicating that these conchs have a preference for that zone. At a seasonal scale, there were no differences in density maybe related with the protection regime that exist at Desembarco del Granma National Park.
Chiquillo-Espitia et al. (1997) found that 18% of the conchs with lip thickness ≥5mm in three fishing zones at Colombia were still immature. In addition, the estimated age at which the conch produces the flared lip is among 3-3.5 years, although it varies between populations and depending on the environmental factors that regulate growth (Alcolado 1976, Appeldoorn 1988). Even after the lip is fully formed, the reproduction capacity is reached some month later (Hesse 1976, Egan 1985, Appeldoorn 1988). In this sense, we have been conservative in the morphometric selection of adult, pending that the necessary histological studies must be performed in this zone, allowing good criteria in the differentiation of adult population.
Appeldoorn (1988) proposed three possible mechanisms to explain the relationship between adult conch density and reproductive success, all related to the density of breeding adults, and Stoner et al. (2012a) mentioned that it is necessary to maintain a density higher than 100ind./ha to ensure ]]>
The low density of adults at Farito in dry season may be explained for the fact that adult conch carry out an ontogenetic migration to deeper zones and then they return to shallow waters to breed (Lagos-Bayona 1994, de Jesús- Navarrete ]]>
et al. 2003). Samplings were conducted on November and Farito is located very close to the communication channel between the reef lagoon and the open sea, and it is possible at that time the migration to shallow areas may not yet have begun. In turn, Laguna presented the highest density of adult conch in cold front season which could be related to the initiation of reproductive aggregations that showed a peak immediately after that, in the rainy season (Fig. 4A). Guafe did ]]>
Despite the high total density of adults in this study, the fishery management strategies for E. gigas ]]>
et al. 2000). This avoids the population imbalance, to maintain the global biomass and to prevent the decrease on size and sexual maturity (Harmelin et al. 1995). ]]>
et al. 2003, Stoner et al. ]]>
et al. 2003, Stoner et al. 2012a) and must be taken into consideration when planning a sustainable fishery of conch at Cabo Cruz.
The high density of adults conch in ]]>
E. gigas (Alcolado 1976) and has been possible to observe reproductive activity throughout the year. The wider reproduction period (aggregation, mating, spawning females and egg masses) has been reported the year round by Cruz (1986) and Corral & Ogawa (1987) at Banco Chinchorro, Mexico. The shortest period (May- September) was reported at Florida (D’Assaro 1965) and ]]>
et al. 1987, Davis et al. 1987, Stoner et al. 1992, Weill & Laughling 1994).
High reproductive activity during the rainy season at Laguna was observed, possibly, because it is protected by the reef crest and has substrate ]]>
T. testudinum, according to Alcolado (1976) this characteristics are suitable for the conch reproduction. Guafe, in shallow waters, has the influence of runoff and the substrate is muddy with much sediment in suspension and Farito is a transition zone between the shallow zone of Laguna and the deep zone of Cabo Cruz, with substrate entirely covered with dense seagrass, so none of the two zones are adequate for the reproduction. Even with these results, it would be useful to develop more detailed studies that allow the identification of reproductive peaks throughout the year and a more ]]>
Reproductive activity and abiotic factors: In the most of animal species the periods of reproduction activity are determined by daylight variations along the year (photoperiod), temperature, food availability and ecological interactions (Martinet & Mondain-Monval 1991). ]]>
et al. (1992) found a linear direct relationship between mating frequency and temperature and they suggested that, as with temperature, photoperiod may influence the production of mature gametes or have a direct effect on the behavior of ]]>
Spawning frequency and the amount of egg masses increases proportionally with temperature showing the importance of this variable in the reproduction of E. gigas as reported by several authors (Alcolado 1976, Stoner et al. 1992, Davis 1998). The significant relationship between mating and spawning frequencies corroborates, in a way, one of the mechanisms proposed by Appeldoorn (1988) that refers a positive feedback between spawning and gametogenesis in females. According to the hypothesis of Appeldoorn (1988), copulation stimulates oocyte development and maturation, leading more frequent spawning.
It is considered that the number of aggregations per zone is related with the search for mating (Brownell & Stevely 1981) and could be linked to food abundance at the substrate features instead of the reproductive activity (Alcolado 1976). Nevertheless it is possible that Guafe has higher values of organic matter in the sediment in relation with the other zones because of coastal runoff (Cala 2006) and a high number of groups feeding should be expected but this did not happen. In Cabo Cruz exists an intense reproductive activity of E. gigas all year round with a high density of adult conchs in the three studied zones. This suggest not only an important stock for this species it the Southeastern shelf of Cuba else a possible self-sufficiency of this population to guarantee a relatively stable recruitment too.
From the previous, an adequate regulatory exploitation of the population is viable taking into account that the Laguna site reached the higher absolute frequency of reproductive evidences during the study period, mostly during the rainy season (March-June). This aspect is important for the establishment of temporal closures and the functional zonation of the protected area. In addition, Laguna zone must be proposed as a reproductive activity area, and Guafe and Farito as potential fishing areas with a closure season from March to June. To conduct a wider spatial and temporal study will first benefit the knowledge of the distribution of this species and second the decision making because it could be proposed a yearly rotation of the fishing zones and a monitoring program of E. gigas and its habitat as part of the National Park Management Plan (Cala 2006).
Acknowledgments
This research was conducted under the support of Consejo Nacional de Ciencia y Tecnología, México, doctoral concession number 228610. Centro Nacional de Áreas Protegidas de Cuba gave field materials. We thank the useful assistance of C. Ocano, O. De la Hera and A. Galindo during field work. Comments of A.W. Stoner, P.M. Alcolado, J.C. Pérez, D. Gonzales and M. Mendoza contributed to improve the manuscript.
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*Correspondencia a Yuself R. Cala. Programa de doctorado en Ecología y Desarrollo Sustentable, El Colegio de la Frontera Sur, Unidad Chetumal. Ave. Centenario, Km. 5,5, Col. Antorchista. Chetumal. Quintana Roo, México; sgigas21824@gmail.com. Alberto de Jesús-Navarrete. Departamento de Aprovechamiento y Manejo de Recursos Acuáticos, El Colegio de la Frontera Sur (ECOSUR), Unidad Chetumal, México; anavarre@ecosur.mx. Frank A. Ocaña. Centro de Investigaciones y Servicios Ambientales y Tecnológicos (CISAT), Holguín, Cuba; frankocisat@gmail.com. José Oliva-Rivera. Departamento de Aprovechamiento y Manejo de Recursos Acuáticos, El Colegio de la Frontera Sur (ECOSUR), Unidad Chetumal, México; joliva@ecosur.mx. ]]>
1. Programa de doctorado en Ecología y Desarrollo Sustentable, El Colegio de la Frontera Sur, Unidad Chetumal. Ave. Centenario, Km. 5,5, Col. Antorchista. Chetumal. Quintana Roo, México; sgigas21824@gmail.com 2. Departamento de Aprovechamiento y Manejo de Recursos Acuáticos, El Colegio de la Frontera Sur (ECOSUR), Unidad Chetumal, México; anavarre@ecosur.mx, joliva@ecosur.mx 3. Centro de Investigaciones y Servicios Ambientales y Tecnológicos (CISAT), Holguín, Cuba; frankocisat@gmail.com
Received 15-II-2012. Corrected 20-IX-2012. Accepted 18-X-2012.
