Printer Friendly

Variacion de la conformacion de la concha del caracol reina Strombus gigas (Caenogastropoda: Strombidae) del Caribe suroccidental.

Shell shape variation of queen conch Strombus gigas (Mesograstropoda: Strombidae) from Southwest Caribbean

The queen conch Strombus gigas Linnaeus, 1758 is a large marine gastropod of significant economic importance through the Greater Caribbean region (Theile, 2005). In this endangered species, the genetic patchiness seems to characterize the natural populations since studies using neutral markers have shown both gene flow (Mitton, Berg, & Orr, 1989; Campton, Berg Jr, Robinson, & Glazer, 1992) and genetic structure either at isolated sites or at micro-scales across different Caribbean areas (Mitton et al., 1989; Tello-Cetina, Rodriguez-Gil, & Rodriguez-Romero, 2005; Marquez et al., 2013).

The morphometrics studies in S. gigas has been used to solve ecological questions of fisheries interest (Randall, 1964; Avila-Poveda & Baqueiro-Cardenas, 2006). Thus, the measures based on shell length and lip thickness to estimate the size at sexual maturity are used as a parameter for management regulations and sustainability of fisheries (Wenner, Fusaro, & Oaten, 1974; Conand, 1981; 1989; Appeldoorn, 1988). However, the morphometric studies have not been used to define phenotypic stocks so far, this information allows to determine the way the stock responds to exploitation. This issue is relevant since the ontogenic rates influence many population attributes that are intimately related to population dynamics (Garrod & Horwood, 1984).

On the other hand, the morphometric studies have documented sexual size dimorphism in S. gigas shell (Randall, 1964; Galindo-Perez, 2009) and other members of the genus Strombus such as S. gibberulus, S. flammeus (Abbott, 1949), S. pugilis (Colton, 1905; Galindo-Perez, 2009), S. canarium (Cob, Arshad, & Idris, 2008), and S. costatus (Galindo-Perez, 2009). Similarly, the sexual shape dimorphism in the shell has been reported in S. gigas, S. costatus (Galindo-Perez, 2009), S. pugilis (Colton, 1905; Galindo-Perez, 2009) and other no phylogenetically related snails like Buccinun undatum (Hallers-Tjabbers, 1979), Nucella lapillus (Son & Hughes, 2000), Pomacea canaliculata (Estebenet, Martin, & Burela, 2006) and Buccinanops globulosus (Avaca, Narvarte, Martin, & Van der Molen, 2013).

In addition, evolutionary studies of shell in S. gigas have evidenced plastic responses to environmental variations (Alcolado, 1976; Stoner & Davis, 1994; Martin-Mora, James, & Stoner, 1995) and to predators under controlled conditions (Delgado, Glazer, & Stewart, 2002). Likewise, the plastic responses to environmental variations have been found in other snail species (Pascoal et al., 2012; Kistner & Dybdahl, 2013; Gustafson, Kensinger, Bolek, & Luttbeg, 2014; Solas, Hughes, Marquez, & Brante, 2015). During ontogeny, these plastic responses to environmental heterogeneity constitute a key factor in the potential of species to colonize, survive and reproduce; abilities that allow them to persist under diverse environmental conditions and expand its distribution range (Stearns, 1989). However, it remains to address whether the variations in shell shape of S. gigas reflect genetic differences as well as it occurs in other gastropods (Johannesson & Johannesson, 1996; Conde-Padin, Caballero, & Rolan-Alvarez, 2009; Martinez-Fernandez, Paes de la Cadena, & Rolan-Alvarez, 2010; Zieritz, Hoffman, Amos, & Aldridge 2010; Pascoal et al., 2012).

Thus, in this work, geometric morphometric analysis was used to address the effect of genetics and geographic origin on S. gigas shell size and shape across a broad area in the Colombian Southwestern Caribbean (San Andres archipelago). In this area, the spatial phenotypic variation of S. gigas shell is unknown, although this information may complement the genetic studies in this region (Marquez et al., 2013). The genetic control of the shell shape cannot be overlooked in populations of S. gigas from Colombian San Andres archipelago because they are structured in three genetically different groups. Furthermore, both the bathymetry of San Andres archipelago (Andrade, 2001) that limit the queen conch dispersion among sites, as well as the environmental and fishing variable conditions, may induce phenotypic differences in the queen conch shells.


Specimens and study area: A total of 219 shells of adult individuals of S. gigas were assessed using geometric morphometric analysis. These samples were collected at different sites in the San Andres archipelago, which are separated by depths ranging from 100 to 1 500 fathoms that impede the dispersal of juveniles and adults among these sites (Fig. 1). In this area, the population genetics of S. gigas shows a moderate genetic structure among three regions of the San Andres archipelago: Southern (South-South-West and East-SouthEast atolls); Northern (Roncador, Queena and Serrana atolls) and most Northern, near to Jamaica (Serranilla atoll, Alice shoal and Bajo Nuevo atoll) (Marquez et al., 2013). On the other hand, the fishing pressure is differential among the sites because some of them are subjected to artisanal (South-South-West and East-South-East atolls, Roncador, Serrana) and industrial fisheries (Queena, Serranilla atoll, Alice shoal and Bajo Nuevo atoll).

Geometric morphometries: Ten landmarks of type II (Bookstein, 1991) were identified on digital photographs of shells (Fig. 2). To reduce peripheral optical distortion, each shell was photographed in the centre of the visual field, and landmarks were digitized twice on the set of 219 shells. Digital precision was estimated by using the "Repeatability" index (individual variance / total variance) in a model II one-way ANOVA on repeated measures (Arnqvist & Martensson, 1998) using VAR module of the software CLIC V.70 (Dujardin, 2013). Raw data of coordinates were submitted to Generalized Procrustes analyses to generate "partial warp" scores and uniform components (Rohlf, 1990; Rohlf & Slice, 1990) as shape variables, using the modules COO and MOG of the software CLIC V.70 (Dujardin, 2013).

Size variation: The isometric estimator known as centroid size was extracted from coordinates and used for size comparisons of the shell. Centroid size is defined as the square root of the sum of the squared distances between the centre of the configuration of landmarks and each individual landmark (Bookstein, 1990). First, the principal effect of sex on centroid size was investigated by a one-way ANOVA in samples from three sites for which data were available (Serranilla atoll, Alice shoal and Bajo Nuevo atoll). To avoid bias depending upon the type of measure of size, the analysis was also performed using siphon longitude as a measure of size. Second, the centroid size among eight sites was compared using one-way ANOVA. All ANOVAs were performed after verified that the assumptions of normality and homoscedasticity were satisfied. A posteriori Bonferroni tests were then conducted to test pairwise treatment comparisons. Finally, to detect correlations between size variation and genetics and geographic position, a multiple regression was performed using the centroid size as a dependent variable and the mean observed heterozygosity previously published (Marquez et al., 2013), latitude and longitude as the independent variables. The method Variance Inflation Factor (VIF) was used to estimate the multicollinearity among independent variables. In residuals, the normality was estimated by Lilliefors test, homoscedasticity by studentized Breusch-Pagan test and autocorrelation by Durbin-Watson. Finally, the Hierarchical Partitioning method was used for calculating the contribution of all independent variables to the regression model. Analysis were conducted in R 2.15.2 (www.r-project. org) and RWizard (Guisande, 2015).

Shape variation: The effect of sex (Serranilla atoll, Alice shoal and Bajo Nuevo atoll) and geographic origin on shell shape of S. gigas from San Andres archipelago was explored by using principal component analysis. Statistical significance between pair-wise Euclidean distances was assessed using 1 000 permutations and multiple comparisons were adjusted by Bonferroni Test (Sokal & Rohlf, 1995). The residual relationship between shape and size variables was explored by multivariate regression and permutation test procedure for statistical significance (Good, 2000). Using MANCOVA (with size as a covariate), we also investigated the model of an allometric trend common to different population and the statistical significance was obtained by the Wilks statistics. The Euclidean distances derived from the first five principal components, which explained 97% of total variation, were used to construct a UPGMA tree (Mega v.6.0; Tamura, Stecher, Peterson, Filipski, & Kumar, 2013). Finally, the relationship among Euclidean distances and heterozygosity differences was evaluated by a Mantel test.


Repeatability: Congruence between two sets of measures from the same set of 219 shell photographs showed fairly good agreement for CS (R = 0.999), as well as for the five relative warps (RW1, RW2, RW3, RW4 and RW5, with R = 0.905, 0.809, 0.817, 0.935, 0.794 respectively) representing most of the shape variation (97%).

Size variation: Centroid size (ShapiroWilks: 0.992, P = 0.982; Barlett Test: 1.000, P = 0.948) and siphon longitude (Shapiro-Wilks: 0.987, P = 0.864; Barlett Test: 1.000, P = 0.887) showed normal distribution and variance homogeneity. Both size measures were not significant between sexes (all P > 0.05). In contrast, the differences of size among sites were significant ([F.sub.(8. 246)] = 52.63; P = 0.000) showing a gradient from South (smallest individuals) to North (largest individuals) (Fig. 3). On the other hand, the multiple regression showed that the variables heterozygosity and latitude explain the 62.9% of the observed variance in the centroid size ([r.sup.2] = 0.629; P < 0.001). These variables did not show multicollinearity (VIF = 1.593) and residuals satisfied the assumptions of normality (KolmogorovSmirnov: 0.056; P = 0.085) and absent of autocorrelation (Durbin-Watson: 1.821; P = 0.072) although they did not show homoscedasticity (Breusch-Pagan: 0.795; P = 0.033).

Shape variation: Sexual shape dimorphism was not significant in all the studied sites (P > 0.160 after Bonferroni correction). However, since the allometric effect was significant (p = 0.000), the variation of shape after correcting for size was evaluated because the hypothesis of a common allometric model was accepted (X Wilks: 0.3869; [F.sub.(80.414)] 1.1271; P = 0.230). Without allometric effect, the sexual shape dimorphism was significant in Alice shoal (Euclidean distance: 0.028; p = 0.000) and Bajo Nuevo atoll (Euclidean distance: 0.027; P = 0.000) but it was non-significant in Serranilla, after Bonferroni correction (Euclidean distance: 0.019; P = 0.028 > 0.003). However, both sexes showed the same topology of the tree according to the geographic origin (Fig. 4). The Euclidean distances among regions and sites were highly significant (Table 1). Additionally, the UPGMA tree clustered the samples in three main groups (Fig. 5): (1) Alice shoal, Serranilla and Bajo Nuevo atolls, (2) Serrana atoll and (3) South-South-West, East-SouthEast, Queena and Roncador atolls. On the other hand, the shell shape variation was not correlated with variations in heterozygosity (r: -0.074; t: -0.348; P = 0.364).


The use of three moderate differentiated genetic groups in this work allowed us to assess the role of genetics and geographical origin on shell size and shape of S. gigas. Non-significant sexual size dimorphism of S. gigas found in this work contrasts with previous studies of this species in other Caribbean regions (Randall, 1964; Avila-Poveda & BaqueiroCardenas, 2006; Galindo-Perez, 2009) but it is concordant with results found in S. pugilis (Galindo-Perez, 2009). This suggests that the sexual size dimorphism may vary among sites, corroborating that the degree of sexual size dimorphism in gastropods may differ among localities as well as found in S. gibberulus and S. flammeus from Indo-Pacific (Abbott, 1949). In other taxa, changes in sexual size dimorphism may result from sexual differences in phenotypic plasticity (Stillwell & Davidowitz, 2010; Marquez & Saldamando-Benjumea, 2013). This may explain the results found in S. gigas because the shell of queen conch is a plastic trait (Alcolado, 1976; Stoner & Davis, 1994; Martin-Mora et al., 1995; Delgado et al., 2002; Clerveaux, Danylchuk, & Clerveaux, 2005) and the habitat exert a high influence on the morphology of juvenile and adults (Martin-Mora et al., 1995).

On the other hand, the sexual shape dimorphism in S. gigas shell is concordant with previous studies in S. gigas, S. costatus (Galindo-Perez, 2009), S. pugilis (Colton, 1905; Galindo-Perez, 2009) and other snails like Buccinun undatum (Hallers-Tjabbers, 1979), Nucella lapillus (Son & Hughes, 2000), Pomacea canaliculata (Avaca et al., 2013). Such variations cannot be explained by allometry since the sexual shape dimorphism was significant after size correction. However, the degree of sexual shape dimorphism varied across sites (it was non-significant in Serranilla) suggesting that this trait may also be plastic.

Geographical comparisons of the size showed that shells of queen conch were significant different among sites. This result is concordant with those found in samples from Puerto Rico (Appeldoorn, 1994), Bahamas (Stoner & Ray-Culp, 2000) and Turks and Caicos (Clerveaux et al., 2005). Furthermore, queen conchs from archipelago displayed an increasing gradient of size from South to North atolls. The size gradient may result from food competition related to population density, which has been reported in other Caribbean areas (Cala de la Hera, De Jesus-Navarrete, Oliva-Rivera, & Ocana-Borrego, 2011) but our results do not show the expected inverse relationship among shell size and population density. Here, largest snails were found in high population density sites, whereas smallest snails were in low population density sites.

Alternatively, the gradient in the shell size may result from fishing pressure. Such decreasing of body and sexual mature size as a result of fishing has been previously described in S. gigas (De Jesus-Navarrete, Medina-Quej, & Oliva-Rivera, 2003; De Jesus-Navarrete & Valencia-Hernandez, 2013). However, this explanation seems unlikely because the size of S. gigas shells were inversely related to the fishery pressure: largest snails were in the sites subjected to industrial fishery, whereas the smallest snails were in the sites subjected to artisanal fishery.

Instead, the size pattern may result from differences in food quality/availability as well as genetic background. A previous study established that the quality and availability of food may affect the growth rate and thus, the total longitude of the S. gigas shell (Alcolado, 1976). Such explanation suggests a gradient of food quality and availability among the atolls likely related to the influence of marine currents since largest individuals are influenced by the Caribbean Central Currents, whereas smallest ones are influenced by the anticyclonic gyre. However, the lack of information about these parameters does not permit to contrast this hypothesis. Additionally, the selective extractions of largest individuals may favour the reproductive success of smallest snails. This explanation is likely since the variation in shell size was directly correlated with the latitude and the levels of heterozygosity of the populations.

On the other hand, the differences in shell shape among sites are consistent with genetic differences and low dispersion of snails among atolls. Morphometric differences are concordant with genetic differences evidenced previously by microsatellites (Marquez et al., 2013) among populations near to Jamaica (Serranilla atoll, Alice shoal and Bajo Nuevo atoll) and the North of Archipelago (Roncador, Queena and Serrana atolls) and between South-South-West and East-South-East atolls. However, morphometric differences were also found among genetically similar populations (Serranilla versus Queena and Roncador) corroborating the role of phenotypic plasticity in the variation of S. gigas shell (Alcolado, 1976; Stoner & Davis, 1994; Martin-Mora et al., 1995; Delgado et al., 2002).

The role of genetic background as well as phenotypic plasticity on the shell shape has been evidenced in other snails such as Littorina saxatilis (Johannesson & Johannesson, 1996; Conde-Padin et al., 2009; Martinez-Fernandez et al., 2010), Unio pictorum (Zieritz et al., 2010) and Nucella lapillus (Pascoal et al. 2012). The influence of both factors on the S. gigas shell shape would explain the lack of correlation between genetic diversity measured by neutral markers and the phenotypic variation, likely submitted to different evolutionary forces. This different behavior of genetic markers was also used to explain the divergence between genetic and morphometric data in other taxa (Marquez, Jaramillo-O, GomezPalacio, & Dujardin, 2011).

In conclusion, the results of this study support the idea that the variation of the shell of S. gigas may be explained by phenotypic plasticity to environmental variation as well as the genetic background. It has been proposed that these two factors may maximise fitness when the environmental circumstances became uncertain by unpredictable changes in local or long distance dispersal (Pascoal et al. 2012). For the fishery stock assessment, groups with different growth or reproduction dynamics should be modelled and managed separately, regardless of genetic homogeneity (Cadrin, Friedland, & Waldman, 2005). Thus, the geometric morphometrics of shell of queen conch may represent a valuable complementary tool in the management and conservation regulations.


This work was funded by the Scientific Cooperation Agreement # 063 de 2008 among Universidad Nacional de Colombia, Sede Medellin, Departamento del Archipielago de San Andres, Providencia y Santa Catalina, Corporacion para el desarrollo sostenible del Archipielago de San Andres, Providencia y Santa Catalina (Coralina) and Instituto Colombiano Agropecuario (ICA). Authors thank to Nacor Bolanos for his help during field collections.


Abbott, R. (1949). Sexual Dimorphism in Indo-Pacific Strombus. Nautilus, 63, 58-61.

Alcolado, P. M. (1976). Crecimiento, variaciones morfologcas de la concha y algunos datos biologicos del cobo Strombus gigas L. (Mollusca, Mesogastropoda). Serie Oceanologica, 34, 1-36.

Andrade, C. A. (2001). Las corrientes superficiales en la cuenca de Colombia observadas con boyas de deriva.

Revista de la Academia Colombiana de Ciencias Exactas, Fisicas y Naturales, 25, 321-335.

Appeldoorn, R. S. (1988). Age determination, growth, mortality and age of first reproduction in adult queen conch, Strombus gigas L., of Puerto Rico. Fisheries Research, 6, 363-378.

Appeldoorn, R. S. (1994). Queen conch management and research: status, needs and priorities. In R. A. Appeldoorn & B. Rodriguez (Eds.), Proceedings on Queen Conch Biology, Fisheries and Mariculture (pp. 301-319). Caracas, Venezuela: Fundacion Cientifica Los Roques.

Arnqvist, G., & Martensson, T.(1998). Measurement error in geometric morphometrics: empirical strategies to assess and reduce its impact on measure of shape. Acta Zoologica, 44, 73-96.

Avaca, M. S., Narvarte, M., Martin, P., & Van der Molen, S. (2013). Shell shape variation in the Nassariid Buccinanops globulosus in northern Patagonia. Helgoland Marine Research, 67, 567-577.

Avila-Poveda, O. H., & Baqueiro-Cardenas, E. R. (2006). Size at sexual maturity in the queen conch Strombus gigas from Colombia. Boletin de Investigaciones Marinas y Costeras, 35, 223-233.

Bookstein, F. L. (1990). Introduction of methods for landmark data. In F. L. Rohlf, & F. J., Bookstein (Eds.), Proceeding of the Michigan Morphometrics Workshop. Special Publication 2 (pp. 215-225). Ann Arbor (Michigan): Museum of Zoology University of Michigan.

Bookstein, F. L. (1991). Morphometric tools for landmark data: geometry and biology. Cambridge: Cambridge University Press.

Cadrin, S. X., Friedland, K. D., & Waldman, J. R. (2005). Stock identification methods-An overview. In S. X. Cadrin, K. D. Friedland, & J. R. Waldman (Eds.),

Stock Identification Methods: Applications in Fishery Science (pp. 3-6). London, United Kingdom: Elsevier Academic Press.

Cala de la Hera, Y. R., De Jesus-Navarrete, A., Oliva-Rivera, J. J., & Ocana-Borrego, F. A. (2011). Autoecology of the Queen Conch (Strombus gigas L. 1758) at Cabo Cruz, Eastern Cuba: Management and Sustainable use Implications. Proceedings of the 56th Annual Gulf and Caribbean Fisheries Institute, 64, 342-348.

Campton, D. E., Berg Jr, C. J., Robison, L. M., & Glazer, R. A. (1992). Genetic patchiness among populations of queen conch Strombus gigas in the Florida Keys and Bimini. Fishery Bulletin, 90, 250-259.

Clerveaux, W., Danylchuk, A. J., & Clerveaux, V. (2005). Variation in queen conch shell morphology: management implications in the Turks and Caicos Islands, BWI. Proceedings of the 56th Annual Gulf and Caribbean Fisheries Institute, 53, 715-724.

Cob, Z. C., Arshad, A., & Idris, M. (2008). Sexual polymorphisms in a population of Strombus canarium Linnaeus, 1758 (Mollusca: Gastropoda) at Merambong shoal, Malaysia. Zoological Studies, 47, 318-325.

Colton, H. S. (1905). Sexual dimorphism in Strombus pugilis. Nautilus, 18, 138-140.

Conand, C. (1981). Sexual cycle of three commercially important holothurian species (Echinodermata) from the lagoon of New Caledonia. Bulletin of Marine Science, 31, 523-543.

Conand, C. (1989) The fishery resources of Pacific island countries. Part 2. Holothurians. (FAO Fisheries Technical Paper, No. 272.2). Rome: FAO.

Conde-Padin, P., Caballero, A. & Rolan-Alvarez, E. (2009). Relative role of genetic determination and plastic response during ontogeny for shell-shape traits subjected to diversifying selection. Evolution, 63, 1356-1363.

De Jesus-Navarrete, A., Medina-Quej, A., & Oliva-Rivera, J.J. (2003). Changes in the queen conch (strombus gigas L.) Population structure at banco Chinchorro, Quintana Roo, Mexico, 1990-1997. Bulletin of Marine Science, 73, 219-229.

De Jesus-Navarrete, A. & Valencia-Hernandez, A. (2013). Declining densities and reproductive activities of the queen conch Strombus gigas (Mesogastropoda: Strombidae) in Banco Chinchorro, Eastern Caribbean, Mexico. Revista de Biologia Tropical, 61, 1671-1679.

Delgado, G. A., Glazer, R. A., & Stewart, N. J. (2002). Predator-induced behavioral and morphological plasticity in the tropical marine gastropod Strombus gigas. Biological Bulletin, 203, 112-120.

Dujardin, J. P. (2013). Clic package for Windows. Institut de Recherches pour le Developpement (IRD. France). (Available in

Estebenet, A. L., Martin, P. R., & Burela, S. (2006). Conchological variation in Pomacea canaliculata and other South American Ampullariidae (Caenogastropoda, Architaenioglossa). Biocell, 30, 329-335.

Galindo-Perez, L. (2009). Estudio morfometrico del dimorfismo sexual de las conchas de especies gastropoda en Venezuela (Tesis de maestria). Universidad del Oriente Nucleo de Sucre, Cumana, Venezuela.

Garrod, D. J., & Horwood, W. (1984). Reproductive Strategies and the Response to Exploitation. In G. Wootton, & R. J. Potts (Eds.), Fish Reproduction: Strategies and Tactics (pp. 367-384). New York, United States: Academic Press.

Good, P. I. (2000). Permutation tests: a practical guide to resampling methods for testing hypotheses. New York, United States: Springer-Verlag.

Guisande, C. (2015). StatR. Available at http://www.ipez. es/RWizard/

Gustafson, K. D., Kensinger, B. J., Bolek, M. G., & Luttbeg, B. (2014). Distinct snail (Physa) morphotypes from different habitats converge in shell shape and size under common garden conditions. Evolutionary Ecology Research, 16, 77-89.

Hallers-Tjabbers, C. C. (1979). Sexual dimorphism in Buccinun undatum L. Malacologia, 118, 13-17.

Johannesson, B., & Johannesson, K. (1996). Population differences in behaviour and morphology in the snail Littorina saxatilis: phenotypic plasticity or genetic differentiation? Journal of Zoology, 240, 475-493. doi:10.1111/j.1469-7998.1996.tb05299.x.

Kistner, E. J., & Dybdahl, M. F. (2013). Adaptive responses and invasion: The role of plasticity and evolution in snail shell morphology. Ecology and Evolution, 3, 424-436. doi:10.1002/ece3.471.

Marquez, E. & Saldamando-Benjumea, C. I. (2013). Rhodnius prolixus and Rhodnius robustus-like (Hemiptera, Reduviidae) wing asymmetry under controlled conditions of population density and feeding frequency. Journal of Bioscience, 38, 549-560.

Marquez, E., Jaramillo-O, N., Gomez-Palacio, A., & Dujardin, J. P. (2011). Morphometric and molecular differentiation of a Rhodnius robustus-like form from R. robustus Larousse, 1927 and R. prolixus Stal, 1859 (Hemiptera, Reduviidae). Acta Tropica, 120, 103-109.

Marquez, E., Landinez-Garcia, R. M., Ospina-Guerrero, S. P., Segura-Caro, J. A., Prada, M., Castro, E., Correa, J. L., & Borda, C. (2013). Genetic analysis of queen conch Strombus gigas from the Southwest Caribbean. Proceedings of the 56th Annual Gulf and Caribbean Fisheries Institute, 65, 410-416.

Martinez-Fernandez, M., Paes de la Cadena, M., & Rolan-Alvarez, E. (2010). The role of phenotypic plasticity on the proteome differences between two sympatric marine snail ecotypes adapted to distinct micro-habitats. BMC Evolutionary Biology, 10, 1-8 doi:10.1186/1471-2148-10-65.

Martin-Mora, E., James, F. C., & Stoner, A. W. (1995). Developmental plasticity in the shell of the queen conch Strombus gigas. Ecology, 76, 981-994.

Mitton, J. B., Berg, C. J., & Orr, K. S. (1989). Population structure, larval dispersal, and gene flow in the queen conch, Strombus gigas, of the Caribbean. The Biological Bulletin, 177, 356-362. doi:10.2307/154159.

Pascoal, S., Carvalho, G., Creer, S., Rock, J., Kawaii, K., Mendo, S., & Hughes, R. (2012). Plastic and heritable components of phenotypic variation in Nucella lapillus: An assessment using reciprocal transplant and common garden experiments. PLoS ONE, 7, 1-11, e30289. doi:10.1371/journal.pone.0030289.

Randall, J. E. (1964). Contributions to the biology of the queen conch, Strombus gigas. Bulletin of Marine Science, 14, 246-295.

Rohlf, F., & Slice, D. (1990). Extensions of the Procrustes method for the optimal superimposition of landmarks. Systematic Biology, 39, 40-59. doi:10.2307/2992207.

Rohlf, F. J. (1990). Morphometrics. Annual Review of Ecology and Systematics, 21, 299-316.

Sokal, R. R., & Rohlf, F. J. (1995). Biometry: the principles and practice of statistics in biological research. San Francisco, United States: WH. Freeman & Co.

Solas, M. R., Hughes, R. N., Marquez, F., & Brante, A. (2015). Early plastic responses in the shell morphology of Acanthina monodon (Mollusca, Gastropoda) under predation risk and water turbulence. Marine Ecology Progress Series, 527, 133-142. doi:10.3354/ meps11221.

Son, M. & Hughes, R. N. (2000). Sexual dimorphism of Nucella lapillus (Gastropoda: Muricidae) in North Wales, UK. Journal of Molluscan Studies, 66, 489-498.

Stearns, S. C. (1989). The evolutionary significance of phenotypic plasticity. BiosScience, 39, 436-445.

Stillwell, R. C., & Davidowitz, G. (2010). Sex differences in phenotypic plasticity of a mechanism that controls body size: implications for sexual size dimorphism. Proceedings. Biological Sciences / The Royal Society, 277, 3819-3826.

Stoner, A.W., & Davis, M. (1994). Experimental outplanting of juvenile queen conch, Strombus gigas: Comparison of wild and hatchery-reared stocks. Fishery Bulletin, 92, 390-411.

Stoner, A.W. & Ray-Culp, M. (2000). Evidence for Allee effects in an over-harvested marine gastropod: Density-dependent mating and egg production. Marine Ecology Progress Series, 202, 297-302. doi:10.3354/ meps202297.

Tamura, K., Stecher, G., Peterson, D., Filip ski, A., & Kumar, S. (2013). MEGA6: Molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution, 30, 2725-2729. doi:10.1093/ molbev/mst197.

Tello-Cetina, J. T., Rodriguez-Gil, L. A., & Rodriguez-Romero, F. (2005). Population genetics of the pink snail Strombus gigas in the Yucatan Peninsula: Implications for its management and fishery. Ciencias Marinas, 31, 379-386.

Theile, S. (2005). Status of the queen conch Strombus gigas stocks, management and trade in the Caribbean: A CITES review. Proceedings of the 56 annual Gulf and Caribbean Fisheries Institute, 53, 675-694.

Wenner, A. M., Fusaro, C., & Oaten, A. (1974). Size at onset of sexual maturity and growth rate in crustacean populations. Canadian Journal of Zoology, 52, 1095-1106. doi:10.1139/z75-046.

Zieritz, A., Hoffman, J. I., Amos, W., & Aldridge, D. C. (2010). Phenotypic plasticity and genetic isolation by distance in the freshwater mussel Unio pictorum (Mollusca: Unionoida). Evolutionary Ecology, 24, 923-938. doi:10.1007/s10682-009-9350-0.

Edna J. Marquez, Natalia Restrepo-Escobar & Francisco L. Montoya-Herrera

Facultad de Ciencias, Universidad Nacional de Colombia, Medellin, Colombia. Calle 59A No 63-20 Bloque 19 A Laboratorio 310, Medellin, Colombia;,,,

Received 15-X-2015.

Corrected 10-VI-2016.

Accepted 11-VII-2016.

Leyenda: Fig. 1. Sitios de muestreo de S. gigas en el archipielago colombiano de San Andres, Caribe suroccidental.

Fig. 1. Sampling sites of queen conch S. gigas from San Colombian Andres archipelago, Southwest Caribbean.

Leyenda: Fig. 2. Diez puntos anatomicos de referencia tipo II empleados como coordenadas para las conchas de S. gigas. La numeracion de los puntos de referencia denota el arreglo seguido durante la digitalizacion.

Fig. 2. Ten landmarks type II measured as coordinates of S. gigas shells. Numbering on the landmarks denotes the arrangement followed during digitization.

Leyenda: Fig. 3. Variacion del tamano centroide (mm) de las conchas de S. gigas del caribe colombiano. SSW: South South West, ESE: East South East, SER: Serrana, QUE: Queena, RON: Roncador, ALI: Alice shoal, NEW: Bajo Nuevo atoll, SLA: Serranilla. Diferentes letras minusculas en las cajas denota significancia estadistica.

Fig. 3. Centroid size (mm) variation of S. gigas shells from Colombian Caribbean. SSW: South South West, ESE: East South East, SER: Serrana, QUE: Queena, RON: Roncador, ALI: Alice shoal, NEW: Bajo Nuevo atoll, SLA: Serranilla. Different lowercase letter on the box denotes statistical significance.

Leyenda: Fig. 4. Arbol UPGMA basado en las distancias euclidianas derivadas de cinco componentes principales que explican el 97% de la variacion total de la concha. Alice shoal (ALI), Bajo Nuevo atoll (NEW) and Serranilla (SLA) atolls.

Fig. 4. UPGMA tree based on Euclidean distance derived from five principal components that explain the 97% of the total variation of the shell. Alice shoal (ALI), Bajo Nuevo atoll (NEW) and Serranilla (SLA) atolls.

Leyenda: Fig. 5. Arbol UPGMA basado en las distancias euclidianas derivadas de cinco componentes principales que explican el 97% de la variacion total de la concha. South South West (SSW), East South East (ESE), Queena (QUE), Roncador (RON), Serrana (SER), Alice shoal (ALI), Bajo Nuevo atoll (NEW), Serranilla (SLA).

Fig. 5. UPGMA tree based on Euclidean distance among sites derived from five principal components that explain the 97% of the total variation of the shell. South South West (SSW), East South East (ESE), Queena (QUE), Roncador (RON), Serrana (SER), Alice shoal (ALI), Bajo Nuevo atoll (NEW), Serranilla (SLA).

Distancia euclidiana (Ed) y significancia estadistica (P) de la
conformacion de la concha de S. gigas entre regiones y sitios de


Euclidean distances (Ed) and statistical significance (P) of S.
gigas shell shape among regions and sampling sites

Pairwise comparisons                                 Ed        P
Among regions
  Southern region            Northern region        0.036   0.037 *
  Southern region            Most Northern region   0.109   0.000 *
  Northern region            Most Northern region   0.120   0.000 *
Within regions-among sites
  Southern region
  SSW                                        ESE    0.056   0.025 *
Northern region
  QUE                                        RON    0.073   0.000 *
  QUE                                        SER    0.129   0.000 *
  RON                                        SER    0.098   0.000 *
Most Northern region
  ALI                                        NEW    0.029   0.000 *
  ALI                                        SLA    0.055   0.000 *
  NEW                                        SLA    0.038   0.000 *

* Denota significancia estadistica. / * Denotes stadistical
COPYRIGHT 2016 Universidad de Costa Rica
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2016 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Marquez, Edna J.; Restrepo-Escobar, Natalia; Montoya-Herrera, Francisco L.
Publication:Revista de Biologia Tropical
Article Type:Report
Date:Dec 1, 2016
Previous Article:Crecimiento y supervivencia de plantulas de cinco especies de arboles en bosques secundarios y pastizales adyacentes en un bosque lluvioso montano...
Next Article:Epitelio germinal permanente y ciclo reproductivo en machos de atractosteus tropicus (lepisosteiformes: lepisosteidae) Tabasco, Mexico.

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters