Testing otolith morphology for measuring marine fish biodiversity

References

Abaad, M., Tuset, V. M., Montero, D., Lombarte, A., Otero-Ferrer, J. L., and Harun, R. (2016). Phenotypic plasticity in wild marine fishes associated with fish-cage aquaculture. Hydrobiologia 765, 343–358.
|  Phenotypic plasticity in wild marine fishes associated with fish-cage aquaculture.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXht12ku7%2FM&md5=a347b98cffae89688427b424db3066aaCAS |

Alós, J., Palmer, M., Linde-Medina, M., and Arlinghaus, R. (2014). Consistent size-independent harvest selection on fish body shape in two recreationally exploited marine species. Ecology and Evolution 4, 2154–2164.
| 25360257PubMed |

Bagge, O. (2004). The biology of the greater weever fish (Trachinus draco) in the commercial fishery of the Kattegat. ICES Journal of Marine Science 61, 933–943.
| The biology of the greater weever fish (Trachinus draco) in the commercial fishery of the Kattegat.Crossref | GoogleScholarGoogle Scholar |

Bookstein, F. L. (1991). ‘Morphometric Tools for Landmark Data: Geometry and Biology.’ (Cambridge University Press: Cambridge, UK.)

Campana, S. E. (2004). ‘Photographic Atlas of Fish Otoliths of the Northwest Atlantic Ocean.’ (NRC Research Press: Ottawa.)

Clabaut, C., Bunje, P. M. E., Salzburger, W., and Meyer, A. (2007). Geometric morphometric analyses provide evidence for the adaptative caracter of the Tanganyikan cichlid fish radiations. Evolution 61, 560–578.
| Geometric morphometric analyses provide evidence for the adaptative caracter of the Tanganyikan cichlid fish radiations.Crossref | GoogleScholarGoogle Scholar | 17348920PubMed |

Clarke, K. R., and Warwick, R. M. (2001). A further biodiversity index applicable to species lists, variation in taxonomic distinctness. Marine Ecology Progress Series 216, 265–278.
| A further biodiversity index applicable to species lists, variation in taxonomic distinctness.Crossref | GoogleScholarGoogle Scholar |

Colloca, F., Cardinale, M., Belluscio, A., and Ardizzone, G. D. (2003). Pattern of distribution and diversity of demersal assemblages in the central Mediterranean Sea. Estuarine, Coastal and Shelf Science 56, 469–480.
| Pattern of distribution and diversity of demersal assemblages in the central Mediterranean Sea.Crossref | GoogleScholarGoogle Scholar |

Cruz, A., and Lombarte, A. (2004). Otolith size and its relationship with colour patterns and sound production. Journal of Fish Biology 65, 1512–1525.
| Otolith size and its relationship with colour patterns and sound production.Crossref | GoogleScholarGoogle Scholar |

D’Onghia, G., Carlucci, R., Maiorano, P., and Panza, M. (2003). Discards from deep-water bottom trawling in the Eastern–Central Mediterranean Sea and effects of mesh size changes. Journal of Northwest Atlantic Fishery Science 31, 245–261.

Deng, X., Wagner, H. J., and Popper, A. N. (2013). Interspecific variations of inner ear structure in the deep-sea fish family Melamphaidae. The Anatomical Record 296, 1064–1082.
| Interspecific variations of inner ear structure in the deep-sea fish family Melamphaidae.Crossref | GoogleScholarGoogle Scholar | 23625740PubMed |

Farré, M., Tuset, V. M., Maynou, F., Recasens, L., and Lombarte, A. (2013). Geometric morphology as an alternative for measuring the diversity of fish assemblages. Ecological Indicators 29, 159–166.
| Geometric morphology as an alternative for measuring the diversity of fish assemblages.Crossref | GoogleScholarGoogle Scholar |

Friedman, M. (2010). Explosive morphological diversification of spiny-finned teleost fishes in the aftermath of the end-Cretaceous extinction. Proceedings. Biological Sciences 277, 1675–1683.
| Explosive morphological diversification of spiny-finned teleost fishes in the aftermath of the end-Cretaceous extinction.Crossref | GoogleScholarGoogle Scholar |

Gaemers, P. A. M. (1983). Taxonomic position of Cichlidae (Pisces, Perciformes) as demonstrated by the morphology of their otoliths. Netherlands Journal of Zoology 34, 566–595.
| Taxonomic position of Cichlidae (Pisces, Perciformes) as demonstrated by the morphology of their otoliths.Crossref | GoogleScholarGoogle Scholar |

Gaston, K. J. (2000). Global patterns in biodiversity. Nature 405, 220–227.
| Global patterns in biodiversity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXjsFyjs7o%3D&md5=e78583eb098697363850f7dfd52f98eeCAS | 10821282PubMed |

Gatz, A. J. (1979). Community organization in fishes as indicated by morphological features. Ecology 60, 711–718.
| Community organization in fishes as indicated by morphological features.Crossref | GoogleScholarGoogle Scholar |

Gauldie, R. W. (1988). Function, form and time-keeping properties of fish otoliths. Comparative Biochemistry and Physiology. A. Comparative Physiology 91, 395–402.
| Function, form and time-keeping properties of fish otoliths.Crossref | GoogleScholarGoogle Scholar |

Gauldie, R. W., and Crampton, J. S. (2002). An eco-morphological explication of individual variability in the shape of the fish otolith: comparison of the otolith of Hoplostethus atlanticus with other species by depth. Journal of Fish Biology 60, 1204–1221.
| An eco-morphological explication of individual variability in the shape of the fish otolith: comparison of the otolith of Hoplostethus atlanticus with other species by depth.Crossref | GoogleScholarGoogle Scholar |

Gerber, S., Eble, G. J., and Neige, P. (2008). Allometric space and allometric disparity: a developmental perspective in the macroevolutionary analysis of morphological disparity. Evolution 62, 1450–1457.
| Allometric space and allometric disparity: a developmental perspective in the macroevolutionary analysis of morphological disparity.Crossref | GoogleScholarGoogle Scholar | 18346223PubMed |

Goatley, C. H. R., Bellwood, D. R., and Bellwood, O. (2010). Fishes on coral reefs: changing roles over the past 240 million years. Paleobiology 36, 415–427.
| Fishes on coral reefs: changing roles over the past 240 million years.Crossref | GoogleScholarGoogle Scholar |

Gosline, W. A. (1994). Function and structure in the paired fins of scorpaeniform fishes. Environmental Biology of Fishes 40, 219–226.
| Function and structure in the paired fins of scorpaeniform fishes.Crossref | GoogleScholarGoogle Scholar |

Guedes, A. P. P., and Araújo, F. G. (2008). Trophic resource partitioning among five flatfish species (Actinopterygii, Pleuronectiformes) in a tropical bay in southeastern Brazil Journal of Fish Biology 72, 1035–1054.
| Trophic resource partitioning among five flatfish species (Actinopterygii, Pleuronectiformes) in a tropical bay in southeastern BrazilCrossref | GoogleScholarGoogle Scholar |

Hammer, Ø., Harper, D. A. T., and Ryan, P. D. (2001). PAST: paleontological statistics software package for education and data analysis. Palaeontologia Electronica 4, art. 4.

Hobson, E. S. (2006). Evolution. In ‘The Ecology of Marine Fishes: California and Adjacent Waters’. (Eds L. J. Allen, D. J. Pondella and D. J. Horn.) pp. 55–80. (California University Press: Berkeley.).

Horodysky, A. Z., Brill, R. W., Warrant, E. J., Musick, J. A., and Latour, R. J. (2008). Comparative visual function in five sciaenid fishes inhabiting Chesapeake Bay. The Journal of Experimental Biology 211, 3601–3612.
| Comparative visual function in five sciaenid fishes inhabiting Chesapeake Bay.Crossref | GoogleScholarGoogle Scholar | 18978225PubMed |

Karr, J. R., and James, F. C. (1975). Eco-morphological configurations and convergent evolution of species and communities. In ‘Ecology and Evolution of Communities’. (Eds M. L. Cody and J. M. Diamond.) pp. 258–291. (Harvard University Press: Cambridge, MA.)

Kassam, D. D., Sato, T., and Yamaoka, K. (2002). Landmark-based morphometric analysis of the body shape of two sympatric species, Ctenopharynx pictus and Otopharynx sp. ‘heterodon nankhumba’ (Teleostei: Cichlidae), from Lake Malawi. Ichthyological Research 49, 340–345.
| Landmark-based morphometric analysis of the body shape of two sympatric species, Ctenopharynx pictus and Otopharynx sp. ‘heterodon nankhumba’ (Teleostei: Cichlidae), from Lake Malawi.Crossref | GoogleScholarGoogle Scholar |

Kasumyan, A. O. (2004). The vestibular system and sense of equilibrium in fish. Journal of Ichthyology 44, 224–268.

L’Abée-Lund, J. H., and Jensen, A. J. (1993). Otoliths as natural tags in the systematics of salmonids. Environmental Biology of Fishes 36, 389–393.
| Otoliths as natural tags in the systematics of salmonids.Crossref | GoogleScholarGoogle Scholar |

Langerhans, R. B., Layman, C. A., Shokrollahi, A. M., and DeWitt, T. J. (2004). Predator-driven phenotypic diversification in Gambusia affinis. Evolution 58, 2305–2318.
| Predator-driven phenotypic diversification in Gambusia affinis.Crossref | GoogleScholarGoogle Scholar | 15562692PubMed |

Lavin, P. A., and McPhail, J. D. (1985). The evolution of freshwater diversity in threespine stickleback (Gasterosteus aculeatus): site-specific differentiation of trophic morphology. Canadian Journal of Zoology 63, 2632–2638.
| The evolution of freshwater diversity in threespine stickleback (Gasterosteus aculeatus): site-specific differentiation of trophic morphology.Crossref | GoogleScholarGoogle Scholar |

Layman, C. A., Langerhans, R. B., and Winemiller, K. O. (2005). Body size, not other morphological traits, characterizes cascading effects in fish assemblage composition following commercial netting. Canadian Journal of Fisheries and Aquatic Sciences 62, 2802–2810.
| Body size, not other morphological traits, characterizes cascading effects in fish assemblage composition following commercial netting.Crossref | GoogleScholarGoogle Scholar |

Limburg, K. E., Walther, Y., Hong, B., Olson, C., and Storå, J. (2008). Prehistoric versus modern Baltic Sea cod fisheries: selectivity across the millennia. Proceedings. Biological Sciences 275, 2659–2665.
| Prehistoric versus modern Baltic Sea cod fisheries: selectivity across the millennia.Crossref | GoogleScholarGoogle Scholar |

Lin, C. H., and Chang, C. W. (2012). ‘Otolith Atlas of Taiwan Fishes’. (National Museum of Marine Biology and Aquarium: Taiwan.)

Lombarte, A., and Cruz, A. (2007). Otolith size trends in marine fish communities from different depth strata. Journal of Fish Biology 71, 53–76.
| Otolith size trends in marine fish communities from different depth strata.Crossref | GoogleScholarGoogle Scholar |

Lombarte, A., and Popper, A. N. (1994). Quantitative analysis of postembryonic hair cell addition in th otolithic endorgans of the inner ear of the European hake, Merluccius merluccius (Gadiformes, Teleostei). The Journal of Comparative Neurology 345, 419–428.
| Quantitative analysis of postembryonic hair cell addition in th otolithic endorgans of the inner ear of the European hake, Merluccius merluccius (Gadiformes, Teleostei).Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2M%2FhsFWisA%3D%3D&md5=5c460e1a53e24fe0188ef2a654ce6d48CAS | 7929910PubMed |

Lombarte, A., Rucabado, J., Matallanas, J., and Lloris, D. (1991). Taxonomía numérica de Nototheniidae en base a la forma de los otolitos. Scientia Marina 55, 413–418.

Lombarte, A., Chic, Ò., Parisi-Baradad, V., Olivella, R., Piera, J., and García-Ladona, E. (2006). A web-based environment from shape analysis of fish otoliths. The AFORO database. Scientia Marina 70, 147–152.

Lombarte, A., Palmer, M., Matallanas, J., Gómez-Zurita, J., and Morales-Nin, B. (2010). Ecomorphological trends and phylogenetic inertia of otolith sagittae in Nototheniidae. Environmental Biology of Fishes 89, 607–618.
| Ecomorphological trends and phylogenetic inertia of otolith sagittae in Nototheniidae.Crossref | GoogleScholarGoogle Scholar |

Loy, A., Busilacchi, S., Costa, C., Ferlin, L., and Cataudella, S. (2000). Comparing geometric morphometrics and outline fitting methods to monitor fish shape variability of Diplodus puntazzo (Teleostea: Sparidae). Aquacultural Engineering 21, 271–283.
| Comparing geometric morphometrics and outline fitting methods to monitor fish shape variability of Diplodus puntazzo (Teleostea: Sparidae).Crossref | GoogleScholarGoogle Scholar |

Luczkovich, J. J., Sprague, M. W., Johnson, S. E., and Pullinger, R. C. (1999). Delimiting spawning areas of weakfish Cynoscion regalis (Family Sciaenidae) in Pamlico Sound, North Carolina using passive hydroacoustic surveys. Bioacoustics 10, 143–160.
| Delimiting spawning areas of weakfish Cynoscion regalis (Family Sciaenidae) in Pamlico Sound, North Carolina using passive hydroacoustic surveys.Crossref | GoogleScholarGoogle Scholar |

MacArthur, R., and Levins, R. (1967). The limiting similarity, convergence, and divergence of coexisting species. American Naturalist 101, 377–385.
| The limiting similarity, convergence, and divergence of coexisting species.Crossref | GoogleScholarGoogle Scholar |

McClain, C. R., Johnson, N. A., and Rex, M. A. (2004). Morphological disparity as a biodiversity metric in lower bathyal and abyssal gastropod assemblages. Evolution 58, 338–348.
| 15068350PubMed |

Monteiro, L., Di Beneditto, A. P. M., Guilhermo, L. H., and Rivera, L. A. (2005). Allometric changes and shape differentiation of sagitta otoliths in sciaenid fishes. Fisheries Research 74, 288–299.
| Allometric changes and shape differentiation of sagitta otoliths in sciaenid fishes.Crossref | GoogleScholarGoogle Scholar |

Motta, P. J., Clifton, K., Hernandez, P., and Eggold, B. T. (1995). Ecomorphological correlates in ten species of subtropical seagrass fishes: diet and microhabitat utilization. Environmental Biology of Fishes 44, 37–60.
| Ecomorphological correlates in ten species of subtropical seagrass fishes: diet and microhabitat utilization.Crossref | GoogleScholarGoogle Scholar |

Nolf, D. (1985). Otolithi piscium. In ‘Handbook of Paleoichthyology’. (Ed. H. P. Schultze.). pp. 1–10. (Gustav Fischer Verlag: Stuttgrat.)

Nolf, D. (2013). ‘The Diversity of Fish Otoliths, Past and Present.’ (Royal Belgian Institute of Natural Sciences: Bruxelles.)

Parisi-Baradad, V., Manjabacas, A., Lombarte, A., Olivella, R., Chic, Ò., Piera, J., and García-Ladona, E. (2010). Automatic taxon identification of teleost fishes in an otolith online database. Fisheries Research 105, 13–20.
| Automatic taxon identification of teleost fishes in an otolith online database.Crossref | GoogleScholarGoogle Scholar |

Paxton, J. R. (2000). Fish otoliths: do sizes correlate with taxonomic group, habitat or luminescence? Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 355, 1299–1303.
| Fish otoliths: do sizes correlate with taxonomic group, habitat or luminescence?Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3M7psF2ruw%3D%3D&md5=6565d031163f38f00933fc3502ab17fcCAS | 11079419PubMed |

Peres-Neto, P. R. (2004). Patterns in the co-occurrence of fish species in streams: the role of site suitability, morphology and phylogeny versus species interactions. Oecologia 140, 352–360.
| Patterns in the co-occurrence of fish species in streams: the role of site suitability, morphology and phylogeny versus species interactions.Crossref | GoogleScholarGoogle Scholar | 15138880PubMed |

Petchey, O. L., and Gaston, K. J. (2006). Functional diversity: back to basics and looking forward. Ecology Letters 9, 741–758.
| Functional diversity: back to basics and looking forward.Crossref | GoogleScholarGoogle Scholar | 16706917PubMed |

Ponton, D. (2006). Is geometric morphometrics efficient for comparing otolith shape of different fish species? Journal of Morphology 267, 750–757.
| Is geometric morphometrics efficient for comparing otolith shape of different fish species?Crossref | GoogleScholarGoogle Scholar | 16526058PubMed |

Popper, A. N., and Coombs, S. (1982). The morphology and evolution of the ear in actinopterygian fishes. American Zoologist 22, 311–328.
| The morphology and evolution of the ear in actinopterygian fishes.Crossref | GoogleScholarGoogle Scholar |

Popper, A. N., and Fay, R. R. (1993). Sound detection and processing by fish: critical review and major research questions. Brain, Behavior and Evolution 41, 14–38.
| Sound detection and processing by fish: critical review and major research questions.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s7mtFSrsA%3D%3D&md5=9af630a303e5543dadebdfcc857c1ebfCAS | 8431753PubMed |

Popper, A. N., and Lu, Z. (2000). Structure–function relationships in fish otolith organs. Fisheries Research 46, 15–25.
| Structure–function relationships in fish otolith organs.Crossref | GoogleScholarGoogle Scholar |

Ramcharitar, J., Higgs, D. M., and Popper, A. N. (2001). Sciaenid inner ears: a study in diversity. Brain, Behavior and Evolution 58, 152–162.
| Sciaenid inner ears: a study in diversity.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD387ns1yqtg%3D%3D&md5=611363fa72875d49709320ddca1abca0CAS | 11910172PubMed |

Ramcharitar, J., Gannon, D. P., and Popper, A. N. (2006). Bioacoustics of the family Sciaenidae (croakers and drumfishes). Transactions of the American Fisheries Society 135, 1409–1431.
| Bioacoustics of the family Sciaenidae (croakers and drumfishes).Crossref | GoogleScholarGoogle Scholar |

Recasens, L., Lombarte, A., and Sánchez, P. (2006). Teleostean fish composition and structure of an artificial reef and a natural rocky area in Catalonia (North Western Mediterranean). Bulletin of Marine Science 78, 71–82.

Reichenbacher, B., and Reichard, M. (2014). Otoliths of five extant species of the Annual Killifish Nothobranchius from the East African Savannah. PLoS One 9, e112459.
| Otoliths of five extant species of the Annual Killifish Nothobranchius from the East African Savannah.Crossref | GoogleScholarGoogle Scholar | 25383789PubMed |

Reichenbacher, B., Sienknecht, U., Küchenhoff, H., and Fenske, N. (2007). Combined otolith morphology and morphometry for assessing taxonomy and diversity in fossil and extant killifish (Aphanius, †Prolebias). Journal of Morphology 268, 898–915.
| Combined otolith morphology and morphometry for assessing taxonomy and diversity in fossil and extant killifish (Aphanius, †Prolebias).Crossref | GoogleScholarGoogle Scholar | 17674357PubMed |

Ricklefs, R. E. (2012). Species richness and morphological diversity of passerine birds. Proceedings of the National Academy of Sciences of the United States of America 109, 14482–14487.
| Species richness and morphological diversity of passerine birds.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsVaqu77I&md5=bb7ab28bcbbcc95dd824c9bf6d8cf3f9CAS | 22908271PubMed |

Rizkalla, S. I., and Philips, A. I. (2008). Feeding habits of the Atlantic stargazer fish Uranoscopus scaber Linnaeus, 1758 (Family: Uranoscopidae) in Egyptian Mediterranean waters. Egyptian Journal of Aquatic Biology and Fisheries 12, 1–11.

Rohlf, F. J. (2003a). ‘TpsDig Version 2.16. Department of Ecology and Evolution.’ (State University of New York at Stony Brook: New York.)

Rohlf, F. J. (2003b). ‘TpsRelw Version 1.49. Department of Ecology and Evolution.’ (State University of New York at Stony Brook: New York.)

Rohlf, F. J., and Marcus, L. F. (1993). A revolution in morphometrics. Trends in Ecology & Evolution 8, 129–132.
| A revolution in morphometrics.Crossref | GoogleScholarGoogle Scholar |

Sadighzadeh, Z., Tuset, V. M., Valinassab, T., Dadpour, M. R., and Lombarte, A. (2012). Comparison of different otolith shape descriptors and morphometrics for the identification of closely related species of Lutjanus spp. from the Persian Gulf. Marine Biology Research 8, 802–814.
| Comparison of different otolith shape descriptors and morphometrics for the identification of closely related species of Lutjanus spp. from the Persian Gulf.Crossref | GoogleScholarGoogle Scholar |

Sadighzadeh, Z., Otero-Ferrer, J. L., Lombarte, A., Fatemi, M. R., and Tuset, V. M. (2014). An approach to unraveling the coexistence of snappers (Lutjanidae) using otolith morphology. Scientia Marina 78, 353–362.
| An approach to unraveling the coexistence of snappers (Lutjanidae) using otolith morphology.Crossref | GoogleScholarGoogle Scholar |

Schoener, T. W. (1974). Resource partitioning in ecological communities. Science 185, 27–39.
| Resource partitioning in ecological communities.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cvgslehtQ%3D%3D&md5=b39953783d925c07e87c67971f4407e9CAS | 17779277PubMed |

Schulz-Mirbach, T., Heß, M., and Metscher, B. D. (2014). Sensory epithelia of the fish inner ear in 3D: studied with high-resolution contrast enhanced micro CT. Frontiers in Zoology 11, 25.
| Sensory epithelia of the fish inner ear in 3D: studied with high-resolution contrast enhanced micro CT.Crossref | GoogleScholarGoogle Scholar | 24645675PubMed |

Schwarzhans, W. (1996). Otoliths from the Maastrichtian of Bavaria and their evolutionary significance. In ‘Mesozoic Fishes: – Systematics and Paleoecology’. (Eds G. Arratia and G Viohl.) pp. 417–431. (Verlag Dr. Friedrich Pfeil: München.).

Smale, M. J., Watson, G., and Hecht, T. (1995). Otolith atlas of southern African marine fishes. Ichthyological Bulletin of the J. L. B. Smith Institute of Ichthyology 1, 1–253.
| Otolith atlas of southern African marine fishes.Crossref | GoogleScholarGoogle Scholar |

Somerfield, P. J., Clarke, R., Warwick, R. M., and Dulvy, N. K. (2008). Average functional distinctness as a measure of the composition of assemblages. ICES Journal of Marine Science 65, 1462–1468.
| Average functional distinctness as a measure of the composition of assemblages.Crossref | GoogleScholarGoogle Scholar |

Stransky, C., Baumann, H., Fevolden, S. E., Harbitz, A., Høie, H., Nedreaas, K. H., Salberg, A. B., and Skarstein, T. (2008). Separation of Norwegian coastal cod and Northeast Arctic cod by outer otolith shape analysis. Fisheries Research 90, 26–35.
| Separation of Norwegian coastal cod and Northeast Arctic cod by outer otolith shape analysis.Crossref | GoogleScholarGoogle Scholar |

Teimori, A., Jawad, L. A. J., Al-Kharusi, L. H., Al-Mamry, J. M., and Reichenbacher, B. (2012). Late Pleistocene to Holocene diversification and historical zoogeography of the Arabian killifish (Aphanius dispar) inferred from otolith morphology. Scientia Marina 76, 637–645.

Torres, G. J., Lombarte, A., and Morales-Nin, B. (2000). Variability of the sulcus acusticus in the sagitta otolith of the genus Merluccius. Fisheries Research 46, 5–13.
| Variability of the sulcus acusticus in the sagitta otolith of the genus Merluccius.Crossref | GoogleScholarGoogle Scholar |

Tuset, V. M., Lombarte, A., González, J. A., Pertusa, J. F., and Lorente, M. J. (2003). Comparative morphology of the sagittae otolith in Serranus spp. Journal of Fish Biology 63, 1491–1504.
| Comparative morphology of the sagittae otolith in Serranus spp.Crossref | GoogleScholarGoogle Scholar |

Tuset, V. M., Rosin, P. L., and Lombarte, A. (2006). Sagittae otolith shape used in the identification of fishes of the genus Serranus. Fisheries Research 81, 316–325.
| Sagittae otolith shape used in the identification of fishes of the genus Serranus.Crossref | GoogleScholarGoogle Scholar |

Tuset, V. M., Lombarte, A., and Assis, C. A. (2008). Otolith atlas for the western Mediterranean, north and central eastern Atlantic. Scientia Marina 72, 1–198.
| Otolith atlas for the western Mediterranean, north and central eastern Atlantic.Crossref | GoogleScholarGoogle Scholar |

Tuset, V. M., Azzurro, E., and Lombarte, A. (2012). Identification of Lessepsian fish species using the sagittae otolith. Scientia Marina 76, 289–299.
| Identification of Lessepsian fish species using the sagittae otolith.Crossref | GoogleScholarGoogle Scholar |

Tuset, V. M., Farré, M., Lombarte, A., Bordes, F., Wienerroither, R., and Olivar, P. (2014). A comparative study of morphospace occupation of mesopelagic fish assemblages from the Canary Islands (north-eastern Atlantic). Ichthyological Research 61, 152–158.
| A comparative study of morphospace occupation of mesopelagic fish assemblages from the Canary Islands (north-eastern Atlantic).Crossref | GoogleScholarGoogle Scholar |

Tuset, V. M., Imondi, R., Aguado, G., Otero-Ferrer, J. L., Santschi, L., Lombarte, A., and Love, M. (2015). Otolith patterns of rockfishes from the Northeastern Pacific. Journal of Morphology 276, 458–469.
| Otolith patterns of rockfishes from the Northeastern Pacific.Crossref | GoogleScholarGoogle Scholar | 25503537PubMed |

Ungaro, N., Marano, G., and Osmani, K. (1998). Demersal fish assemblage diversity as an index of fishery resources exploitation. The Italian Journal of Zoology 65, 511–516.
| Demersal fish assemblage diversity as an index of fishery resources exploitation.Crossref | GoogleScholarGoogle Scholar |

Van Neer, W., Ervynck, A., Bolle, L., Millner, R., and Rijnsdorp, A. D. (2002). Fish otoliths and their relevance to archaelogy: an analysis of medieval, post-medieval, and recent material of plaice, cod, and haddock from the North Sea. Environmental Archaeology 7, 61–76.
| Fish otoliths and their relevance to archaelogy: an analysis of medieval, post-medieval, and recent material of plaice, cod, and haddock from the North Sea.Crossref | GoogleScholarGoogle Scholar |

Vellend, M., Cornwell, W. K., Magnuson-Ford, K., and Mooers, A. (2011). Measuring phylogenetic biodiversity. In ‘Biological Diversity: Frontiers in Measurement and Assessment’. (Eds A. E. Magurran and B. J. McGill.) pp. 194–207. (Oxford University Press: Oxford, UK.)

Vignon, M., and Morat, F. (2010). Environmental and genetic determinant of otolith shape revealed by a non-indigenous tropical fish. Marine Ecology Progress Series 411, 231–241.
| Environmental and genetic determinant of otolith shape revealed by a non-indigenous tropical fish.Crossref | GoogleScholarGoogle Scholar |

Villéger, S., Miranda, J. R., Hernandez, D. F., and Mouillot, D. (2010). Contrasting changes in taxonomic and functional diversity of tropical fish communities after habitat degradation. Ecological Applications 20, 1512–1522.
| Contrasting changes in taxonomic and functional diversity of tropical fish communities after habitat degradation.Crossref | GoogleScholarGoogle Scholar | 20945756PubMed |

Volpedo, A. V., and Echeverría, D. D. (2000). ‘Catálogo y claves de otolitos para la identificación de peces del Mar Argentino. 1. Peces de Importáncia Económica.’ (Dunken: Buenos Aires.)

Volpedo, A. V., and Echeverría, D. D. (2003). Ecomorphological patterns of the sagitta in fish on the continental shelf off Argentine. Fisheries Research 60, 551–560.
| Ecomorphological patterns of the sagitta in fish on the continental shelf off Argentine.Crossref | GoogleScholarGoogle Scholar |

Volpedo, A. V., Tombari, A. D., and Echeverría, D. D. (2008). Ecomorphological patterns of the sagitta of Antarctic fish. Polar Biology 31, 635–640.
| Ecomorphological patterns of the sagitta of Antarctic fish.Crossref | GoogleScholarGoogle Scholar |

Wainwright, P. C., and Richard, B. A. (1995). Predicting patterns of prey use from morphology of fishes. Environmental Biology of Fishes 44, 97–113.
| Predicting patterns of prey use from morphology of fishes.Crossref | GoogleScholarGoogle Scholar |

Wainwright, P. C., Belwood, D. R., and Westneat, M. W. (2002). Ecomorphology of locomotion in labrid fishes. Environmental Biology of Fishes 65, 47–62.
| Ecomorphology of locomotion in labrid fishes.Crossref | GoogleScholarGoogle Scholar |

Walker, J. A. (2010). An integrative model of evolutionary covariance: a symposium on body shape in fishes. Integrative and Comparative Biology 50, 1051–1056.
| An integrative model of evolutionary covariance: a symposium on body shape in fishes.Crossref | GoogleScholarGoogle Scholar | 21558259PubMed |

Weissburg, M. J. (2005). Sensory biology: linking the internal and external ecologies of marine organisms. Marine Ecology Progress Series 287, 263–307.
| Sensory biology: linking the internal and external ecologies of marine organisms.Crossref | GoogleScholarGoogle Scholar |

Werdelin, L., and Lewis, M. E. (2013). Temporal change in functional richness and evenness in the Eastern African Plio–Pleistocene carnivoran guild. PLoS One 8, e57944.
| Temporal change in functional richness and evenness in the Eastern African Plio–Pleistocene carnivoran guild.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXktlSqtbc%3D&md5=80b0d60214c53585e2177f6524a304e3CAS | 23483948PubMed |

Winemiller, K. O. (1991). Ecomorphological diversification in lowland fresh-water fish assemblages from five biotic regions. Ecological Monographs 61, 343–365.
| Ecomorphological diversification in lowland fresh-water fish assemblages from five biotic regions.Crossref | GoogleScholarGoogle Scholar |

Yamanoue, Y., Setiamarga, D. H. E., and Matsuura, K. (2010). Pelvic fins in teleosts: structure, function and evolution. Journal of Fish Biology 77, 1173–1208.
| Pelvic fins in teleosts: structure, function and evolution.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cbjvV2jtw%3D%3D&md5=c7409dc7a644af1abaed2090c929ccc0CAS | 21039499PubMed |

Zelditch, M. L., Sheets, H. D., and Fink, W. L. (2003). The ontogenic dynamics of shape disparity. Paleobiology 29, 139–156.
| The ontogenic dynamics of shape disparity.Crossref | GoogleScholarGoogle Scholar |