Geographic variation in otolith morphology among freshwater populations of Aphanius dispar (Teleostei, Cyprinodontiformes) from the southeastern Arabian Peninsula
Abstract:Aphanius Nardo is a large genus of teleost fishes in the Old World, with 19 described species. Several of these species have only recently been recognized and additional species can be expected from isolated populations in remote areas. We show here that otolith morphology and statistical analyses of otolith variables can contribute to the detection of genetic differentiation in Aphanius. We studied samples of eight Aphanius dispar populations from the southeastern part of the Arabian Peninsula. Two population… Show more
“…The relationship between fish size and otolith shape reflects the combined effects of ontogeny and the environment on otolith shape (Vignon 2012). The overall species-specific shape of the otolith and the nature of its development during ontogeny from the circular larval otolith to the more complex morphology of the adult otolith is genetically determined (Hüssy 2008;Reichenbacher et al 2009;Vignon and Morat 2010), with exogenous factors having a modulating effect through, for example, the effects of feeding and growth on the nature of crystal formation (Gauldie and Nelson 1990) and the rate of protein accretion in the otolith (Hüssy 2008). The shape of the otolith may also reflect its physiological function in hearing and balance, and such variation can have an adaptive significance.…”
Abstract. Two stocks of bluefin tuna (Thunnus thynnus) inhabit the north Atlantic; the western and eastern stocks spawn in the Gulf of Mexico and the Mediterranean Sea respectively. Trans-Atlantic movements occur outside spawning time whereas natal homing maintains stock structure. Commercial fisheries may exploit a mixed assemblage of both stocks. The incorporation of mixing rates into stock assessment is precluded by uncertainties surrounding stock discrimination. Otolith shape descriptors were used to characterise western and eastern stocks of Atlantic bluefin tuna in the present study and to estimate stock composition in catches of unknown origin. Otolith shape varied with length and between locations and years. Within a restricted size range (200-297-cm fork length (FL)) the two stocks were distinguished with an accuracy of 83%. Bayesian stock mixture analysis indicated that samples from the east Atlantic and Mediterranean were predominantly of eastern origin. The proportion assigned to the eastern stock showed slight spatial variation; however, overlapping 95% credible intervals indicated no significant difference (200-297 cm FL: central Atlantic, 73-100%; Straits of Gibraltar, 73-100%; Morocco, 50-99%; Portugal 64-100%). Otolith shape could be used in combination with other population markers to improve the accuracy of mixing rate estimates for Atlantic bluefin tuna.
“…The relationship between fish size and otolith shape reflects the combined effects of ontogeny and the environment on otolith shape (Vignon 2012). The overall species-specific shape of the otolith and the nature of its development during ontogeny from the circular larval otolith to the more complex morphology of the adult otolith is genetically determined (Hüssy 2008;Reichenbacher et al 2009;Vignon and Morat 2010), with exogenous factors having a modulating effect through, for example, the effects of feeding and growth on the nature of crystal formation (Gauldie and Nelson 1990) and the rate of protein accretion in the otolith (Hüssy 2008). The shape of the otolith may also reflect its physiological function in hearing and balance, and such variation can have an adaptive significance.…”
Abstract. Two stocks of bluefin tuna (Thunnus thynnus) inhabit the north Atlantic; the western and eastern stocks spawn in the Gulf of Mexico and the Mediterranean Sea respectively. Trans-Atlantic movements occur outside spawning time whereas natal homing maintains stock structure. Commercial fisheries may exploit a mixed assemblage of both stocks. The incorporation of mixing rates into stock assessment is precluded by uncertainties surrounding stock discrimination. Otolith shape descriptors were used to characterise western and eastern stocks of Atlantic bluefin tuna in the present study and to estimate stock composition in catches of unknown origin. Otolith shape varied with length and between locations and years. Within a restricted size range (200-297-cm fork length (FL)) the two stocks were distinguished with an accuracy of 83%. Bayesian stock mixture analysis indicated that samples from the east Atlantic and Mediterranean were predominantly of eastern origin. The proportion assigned to the eastern stock showed slight spatial variation; however, overlapping 95% credible intervals indicated no significant difference (200-297 cm FL: central Atlantic, 73-100%; Straits of Gibraltar, 73-100%; Morocco, 50-99%; Portugal 64-100%). Otolith shape could be used in combination with other population markers to improve the accuracy of mixing rate estimates for Atlantic bluefin tuna.
“…2; see Reichenbacher et al 2009a). In addition, a total of 60 specimens from southern Iran were studied, i.e.…”
Section: Samples For Comparisonmentioning
confidence: 99%
“…According to the habitat descriptions for A. dispar from the United Arab Emirates and southern Iran (Reichenbacher et al 2009a, Teimori et al 2012a and own observations at the sites in Oman, the general environmental conditions of the sites are comparable, i.e. all are shallow pools, the water energy is low, temperature and pH are generally within the range of 25-28°C and pH 8.0-9.5, and salinity is about 0.05-3%.…”
Section: Samples For Comparisonmentioning
confidence: 99%
“…The principal habitats of A. dispar are coastal lagoons, but also inland waters such as endorheic drainage systems and hot springs (Krupp 1983, Wildekamp 1993, Abdoli 2000. Pronounced intraspecific differences are known to exist in morphological characters of the individuals and otolith traits (Wildekamp 1993, Reichenbacher et al 2009a, Teimori et al 2012a). These differences suggest that some of the landlocked populations have been isolated since the last humid phase of the Holocene, approximately 5500 years ago (Preusser 2009), and perhaps represent species in statu nascendi.…”
SUMMARY:Aphanius dispar (Rüppell, 1829) is a common marine-euryhaline teleost fish in the Near East that has undergone considerable intraspecific differentiation. Otolith morphology is used to analyse the diversity within A. dispar in the Gulf of Oman (Sea of Oman) and the Persian Gulf. A total of 134 individuals from lagoons and inland habitats of Oman, the United Arab Emirates and southern Iran are analysed. The results revealed that otolith traits that are under genetic control are strikingly different from those that are under the influence of environmental factors. A clear spatial structure of the populations is detectable, suggesting that the environmental flexibility of A. dispar, vicariance events during the last glacial maximum (21000-18000 BP), dispersal in the course of the Early Holocene sea-level rise, and Holocene to presentday interruption of gene flow at the Strait of Hormuz have shaped the intraspecific differentiation of A. dispar. These factors may also be responsible for diversification within other marine-euryhaline fishes in the Near East and Mediterranean Sea, and thus the findings can contribute to successful conservation management.
“…The results of this study shed new light on previous work on the differences in otolith morphology between populations of Aphanius iberus (Reichenbacher and Sienknecht 2001) and A. dispar (Reichenbacher et al 2009a, 2009b, Teimori et al 2012a, 2012b. In these studies, otolith differences have been interpreted as indicating allopatric genetic divergence, but a test of this interpretation by molecular data analyses has not been conducted.…”
SUMMARY: Inter-population differences in otolith shape, morphology and chemistry have been used effectively as indicators for stock assessment or for recognizing environmental adaptation in fishes. However, the precise parameters that affect otolith morphology remain incompletely understood. Here we provide the first direct support for the hypothesis that inter-population differences in otolith morphology are genetically encoded. The study is based on otolith morphology and two mitochondrial markers (D-loop, 16S rRNA) of three natural populations of Aphanius fasciatus (Teleostei: Cyprinodontidae) from Southeast Tunisia. Otolith and genetic data yielded congruent tree topologies. Divergence of populations likely results from isolation events in the course of the Pleistocene sea level drops. We propose that otolith morphology is a valuable tool for resolving genetic diversity also within other teleost species, which may be important for ecosystem management and conservation of genetic diversity. As reconstructions of ancient teleost fish faunas are often solely based on fossil otoliths, our discoveries may also lead to a new approach to research in palaeontology.Keywords: Cyprinodontidae, phylogeography, gene flow, local adaptation, otolith morphometry, mitochondrial markers. RESUMEN: Las diferencias inter-pobLacionaLes en La morfoLogía deL otoLito de AphAnius fAsciAtus (cyprinodontiformes) se codifican genéticamente. -Las diferencias en la forma del otolito entre poblaciones, la morfología o la química se han utilizado con efectividad como indicadores para la gestión de poblaciones o para el reconocimiento de adaptaciones ambientales en peces. Sin embargo, los parámetros precisos que afectan la morfología del otolito permanecen sin ser entendidos completamente. Aquí nosotros presentamos la primera evidencia directa para la hipótesis de que las diferencias inter-poblacionales en la morfología del otolito están codificadas genéticamente. El estudio se basa en la morfología del otolito y dos marcadores mitocondriales (D-loop, 16S rRNA) de tres poblaciones naturales de Aphanius fasciatus (Teleostei: Cyprinodontidae) del sudeste de Tunez. Los datos de otolitos y genéticos ofrecen tres topologías congruentes. Aparentemente la divergencia entre poblaciones resulta de los procesos de aislamiento durante los descensos del nivel del mar en el Pleistoceno. Proponemos que la morfología del otolito es una herramienta muy valiosa para entender la diversidad genética también con otras especies de peces, que puede ser importante para la gestión de los ecosistemas y la conservación de la diversidad genética. Ya que las reconstrucciones de la fauna antigua de peces teleósteos se basan a menudo en otolitos fósiles, nuestro hallazgo puede también ser importante como nueva aproximación en las investigaciones palentológicas.
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