Population structure of the pearly razorfish, Xyrichtys novacula (Actinopterygii: Labridae), in sand-seagrass mosaics: spatial variation according to habitat features and sampling techniques
DOI:
https://doi.org/10.3989/scimar.04219.05AKeywords:
habitat, structural complexity, soft bottoms, sediments, sex ratioAbstract
Habitat structure affects the distribution of fishes, particularly across reef-dominated habitats, but few studies have connected patterns in the abundance of soft-bottom fishes with the structure of the habitat. The spatial and temporal patterns of variation in the abundance, biomass and population structure of the pearly razorfish, Xyrichtys novacula, inhabiting sand-Cymodocea nodosa seagrass mosaics were described through two complementary techniques: underwater visual counts and seine nets. We sought to analyse whether biotic (seagrass shoot density, leaf length and meadow cover) and abiotic (sediment composition and particle size) structural elements explained variation in patterns of abundance and biomass. Underwater visual counts registered a larger abundance of individuals and proved significant variation in fish abundance and biomass at the scale of locations, which was otherwise not detected through seine nets. Seasonal variation in fish abundance and biomass was, in all cases, minor. Habitat structural elements helped to explain patterns in fish abundance and biomass. This fish species was particularly abundant in sediments dominated by coarse sands in continuous meadows of C. nodosa ( > 90% seagrass cover) with intermediate densities of 500 to 1000 shoots m–2, followed by large-sized seagrass patches with >1000 shoots m–2. A trade-off between protection provided by seagrass canopies and protection derived from its burial behaviour, limited under high seagrass shoot densities, may explain spatial variation patterns.
Downloads
References
Alós J., Cabanellas-Reboredo M., Lowerre-Barbieri S. 2012. Diel behaviour and habitat utilisation by the pearly razorfish during the spawning season. Mar. Ecol. Prog. Ser. 460: 207-220. http://dx.doi.org/10.3354/meps09755
Anderson M.J. 2001. Permutation tests for univariate or multivariate analysis of variance and regression. Can. J. Fish. Aquat. Sci. 58: 626-639. http://dx.doi.org/10.1139/f01-004
Barberá C., Tuya F., Boyra A., et al. 2005. Spatial variation in the structural parameters of Cymodocea nodosa seagrass meadows in the Canary Islands. Bot. Mar. 48: 122-126. http://dx.doi.org/10.1515/BOT.2005.021
Battaglia P., Castriota L., Consoli P., et al. 2010. Age and growth of pearly razorfish, Xyrichtys novacula (Linnaeus 1758), in the central Mediterranean Sea. J. Appl. Ichthyol. 26: 410-415. http://dx.doi.org/10.1111/j.1439-0426.2009.01383.x
Beltrano A.M., Cannizzaro L., Vitale S., et al. 2006. Preliminary study on the feeding habits of cleaver wrasse Xyrichthys novacula (Pisces: Labridae) in the Strait of Sicily (Mediterranean Sea). Electron. J. Ichthyol. 2: 50-54.
Bentivegna F., Rasotto M.B. 1987. Protogynous hermaphroditism in Xyrichthys novacula (L. 1758). Cybium 11: 75-78.
Boström C., Jackson E.L., Simenstad C.A. 2006. Seagrass landscapes and their effects on associated fauna: A review. Estuar. Coast. Shelf Sci. 68: 383-403. http://dx.doi.org/10.1016/j.ecss.2006.01.026
Box A., Grau A.M., Blanco A., et al. 2009. Els raors (Xyrichthys novacula) a la Reserva dels Freus d'Eivissa i Formentera; efecte de la protecció espacial. Boll. Soc. Hist. Nat. Illes Balears 52: 193-201.
Box A., Deudero S., Blanco A., et al. 2010. Differences in £_13C and £_15N stable isotopes in the pearly razorfish Xyrichtys novacula related to the sex, location and spawning period. J. Fish Biol. 76: 2370-2381. http://dx.doi.org/10.1111/j.1095-8649.2010.02627.x PMid:20557597
Brito A., Pascual P.J., Falcón J.M., et al. 2002. Peces de las Islas Canarias. Catálogo comentado e ilustrado. Francisco Lemus Editor, La Laguna, 419 pp.
Candi G., Castriota L., Andaloro F., et al. 2004. Reproductive cycle and sex inversion in razor fish, a protogynous labrid in the southern Mediterranean Sea. J. Fish Biol. 64: 1498-1513. http://dx.doi.org/10.1111/j.0022-1112.2004.0404.x
Cardinale M., Colloca F., Ardizzone G.D. 1997. Feeding ecology of Mediterranean razorfish Xyrichthys novacula in the Tyrrhenian Sea (central Mediterranean Sea). J. Appl. Ichthyol. 13: 105-111. http://dx.doi.org/10.1111/j.1439-0426.1997.tb00109.x
Cardinale M., Colloca F., Ardizzone G.D. 1998. Growth and reproduction of Xyrichthys novacula (Pisces: Labridae) in the Mediterranean Sea. Sci. Mar. 62: 193-201. http://dx.doi.org/10.3989/scimar.1998.62n3193
Castriota L., Scarabello M.P., Finoia M.G., et al. 2005a. Food and feeding habits of pearly razorfish, Xyrichtys novacula (Linnaeus, 1758), in the southern Tyrrhenian Sea: Variation by sex and size. Environ. Biol. Fish. 72: 123-133. http://dx.doi.org/10.1007/s10641-004-6576-0
Castriota L., Finoia M.G., Andaloro F. 2005b. Trophic interactions between Xyrichtys novacula (Labridae) and juvenile Pagrus pagrus (Sparidae) in the central Mediterranean Sea. Electron. J. Ichthyol. 2: 54-60.
Castriota L., Falautano M., Finoia M.G., et al. 2010. Temporal variations in the diet of pearly razorfish Xyrichtys novacula (Osteichthyes: Labridae). J. Fish Biol. 76: 1626-1639. http://dx.doi.org/10.1111/j.1095-8649.2010.02599.x PMid:20557620
Espino F. 2004. Una metodología para el estudio de las fanerógamas marinas en Canarias. Rev. Acad. Canar. Cienc. 15: 237-256.
Espino F., Tuya F., Brito A., et al. 2011a. Ichthyofauna associated with Cymodocea nodosa meadows in the Canarian Archipelago (central eastern Atlantic): Community structure and nursery function. Cienc. Mar. 37: 157-174. http://dx.doi.org/10.7773/cm.v37i2.1720
Espino F., Tuya F., Brito A., et al. 2011b. Spatial variability in the structure of the ichthyofauna associated with Cymodocea nodosa seagrass meadows across the Canary Islands, north-eastern subtropical Atlantic. Rev. Biol. Mar. Oceanogr. 46: 391-403. http://dx.doi.org/10.4067/S0718-19572011000300009
Espino F., González J.A., Haroun R., et al. 2015. Abundance and biomass of the parrotfish Sparisoma cretense in seagrass meadows: temporal and spatial differences between seagrass interiors and seagrass adjacent to reefs. Environ. Biol. Fish. 98: 121-133. http://dx.doi.org/10.1007/s10641-014-0241-z
Ferrell J.D., Bell J.D. 1991. Differences among assemblages of fish associated with Zostera capricorni and bare sand over a large spatial scale. Mar. Ecol. Prog. Ser. 72: 15-24. http://dx.doi.org/10.3354/meps072015
Fischer W., Bauchot M.L., Schneider M. 1987. Fiches FAO d'identification des espèces pour les besoins de la pêche. (Rév. 1). Méditerranée et Mer Noire. Zone de Pêche 37. Vertébrés, Vol. 2. FAO. Rome. p. 1152.
Franco A., Pérez-Ruzafa A., Drouineau H., et al. 2012. Assessment of fish assemblages in coastal lagoon habitats: Effect of sampling gear method. Estuar. Coast. Shelf Sci. 112: 115-125. http://dx.doi.org/10.1016/j.ecss.2011.08.015
Franquet F., Brito A. 1995. Especies de interés pesquero de Canarias. Consejería de Pesca y Transportes del Gobierno de Canarias, Santa Cruz de Tenerife, 143 pp. PMid:8539665 PMCid:PMC1021326
Froese R., Pauly D. (eds). 2015. FishBase. World Wide Web electronic publication. www.fishbase.org, February 2015.
González-Ortiz V., Alcazar P., Vergara J.J., et al. 2014. Effects of two antagonistic ecosystem engineers on infaunal diversity. Estuar. Coast. Shelf Sci. 139: 20-26. http://dx.doi.org/10.1016/j.ecss.2013.12.015
Goshima S., Peterson C.H. 2012. Both below- and aboveground shoalgrass structure influence whelk predation on hard clams. Mar. Ecol. Prog. Ser. 451: 75-92. http://dx.doi.org/10.3354/meps09587
Gratwicke B., Speight M.R. 2005. The relationship between fish species richness, abundance and habitat complexity in a range of shallow tropical marine habitats. J. Fish Biol. 66: 650-667. http://dx.doi.org/10.1111/j.0022-1112.2005.00629.x
Gray C.A., McElligott D.J., Chick R.C. 1996. Intra- and inter-estuary differences in assemblages of fishes associated with shallow seagrass and bare sand. Mar. Freshw. Res. 47: 723-735. http://dx.doi.org/10.1071/MF9960723
Guidetti P. 2000. Differences among fish assemblages associated with nearshore Posidonia oceanica seagrass beds, rocky-algal reefs and unvegetated sand habitats in the Adriatic Sea. Estuar. Coast. Shelf Sci. 50: 515-529. http://dx.doi.org/10.1006/ecss.1999.0584
Guidetti P., Bussotti S. 2002. Effects of seagrass canopy removal on fish in shallow Mediterranean seagrass (Cymodocea nodosa and Zostera noltii) meadows: a local-scale approach. Mar. Biol. 140: 445-453. http://dx.doi.org/10.1007/s00227-001-0725-1
Guidetti P., Lorenti M., Buia M.C., et al. 2002. Temporal dynamics and biomass partitioning in three Adriatic seagrass species: Posidonia oceanica, Cymodocea nodosa, Zostera marina. Mar. Ecol. 23: 51-67. http://dx.doi.org/10.1046/j.1439-0485.2002.02722.x
Gullström M., Bodin M., Nilsson P.G., et al. 2008. Seagrass structural complexity and landscape configuration as determinants of tropical fish assemblage composition. Mar. Ecol. Prog. Ser. 363: 241-255. http://dx.doi.org/10.3354/meps07427
Hensgen G.M., Holt G.J., Holt S.A., et al. 2014. Landscape pattern influences nekton diversity and abundance in seagrass meadows. Mar. Ecol. Prog. Ser. 507: 139-152. http://dx.doi.org/10.3354/meps10818
Herrera A., Landeira J.M., Tuya F., et al. 2014. Seasonal variability of suprabenthic crustaceans associated with Cymodocea nodosa seagrass meadows off Gran Canaria (eastern Atlantic). Cont. Shelf Res. 88: 1-10. http://dx.doi.org/10.1016/j.csr.2014.06.014
Hori M., Suzuki T., Monthum Y., et al. 2009. High seagrass diversity and canopy-height increased associated fish diversity and abundance. Mar. Biol. 156: 1447-1458. http://dx.doi.org/10.1007/s00227-009-1184-3
Horinouchi M. 2009. Horizontal gradient in fish assemblages structures in and around seagrass habitat: some implications for seagrass habitat conservation. Ichthyol. Res. 56: 109-125. http://dx.doi.org/10.1007/s10228-008-0070-1
Katsanevakis S. 2005. Habitat use by the pearly razorfish, Xyrichtys novacula (Pisces: Labridae). Sci. Mar. 69: 223-229. http://dx.doi.org/10.3989/scimar.2005.69n2223
Lieske E., Myers R. 1994. Collins pocket guide. Coral Reef Fishes. Indo-Pacific and Caribbean including the Red Sea. Harper Collins, New York, 400 pp. PMCid:PMC44323
Marconato A., Tessari V., Marin G. 1995. The mating system of Xyrichthys novacula: Sperm economy and fertilization success. J. Fish Biol. 47: 292-301. http://dx.doi.org/10.1111/j.1095-8649.1995.tb01896.x
Mercader L. 1991. External morphology of the juveniles of Xyrichthys novacula (Linnaeus, 1758) (Pisces, Labridae) from the littoral of Palamós (NW Mediterranean). Misc. Zool. 15: 243-246.
Ministerio de Medio Ambiente. 2002. Estudio Ecocartográfico del Arco Sur de la isla de Gran Canaria. Gobierno de Espa-a. Madrid.
Navarro-Pérez E., Barton E.D. 2001. Seasonal and interannual variability of the Canary Current. Sci. Mar. 65: 205-213.
Nemtzov S.C. 1994. Intraspecific variation in sand-diving and predator avoidance behavior of green razorfish, Xyrichtys splendens (Pisces, Labridae): effect on courtship and mating success. Environ. Biol. Fish. 41: 403-414. http://dx.doi.org/10.1007/BF02197856
Oliver M., Massutí M. 1952. El raó, Xyrichthys novacula (Fam. Labridae). Notas biológicas y biométricas. Bol. Inst. Esp. Oceanogr. 45: 1-15.
Peterson C.H. 1982. Clam predation by whelks (Busycon spp.): Experimental tests of the importance of prey size, prey density, and seagrass cover. Mar. Biol. 66: 159-170. http://dx.doi.org/10.1007/BF00397189
Riera F., Linde M. 2001. El raor, Xyrichthys novacula (Linnaeus, 1758). In: El raor i la cirviola. Conèixer per preservar. Govern de les Illes Balears, Conselleria d'Agricultura i Pesca. Quaderns de Pesca 6: 9-34.
Sachs L. 1982. Applied Statistics: A Handbook of Techniques. Springer-Verlag, New York, 706 pp. http://dx.doi.org/10.1007/978-1-4684-0123-3
Schneider W. 1990. FAO Species Identification Guide for Fishery Purposes. Field Guide to the Commercial Marine Resources of the Gulf of Guinea. FAO, Rome, 268 pp.
Sokal R.R., Rohlf F.J. 2012. Biometry: The Principles and Practice of Statistics in Biological Research. 4th Edition. W.H. Freeman and Company, New York, 937 pp.
Tuya F., Pérez J., Medina L., et al. 2001. Seasonal variation of the macrofauna from three seagrass meadows of Cymodocea nodosa off Gran Canaria (Central-Eastern Atlantic Ocean). Cienc. Mar. 27: 223-234.
Tuya F., Boyra A., Sánchez-Jerez P., et al. 2004. Relationships between rocky-reef fish assemblages, the sea urchin Diadema antillarum and macroalgae throughout the Canarian Archipelago. Mar. Ecol. Prog. Ser. 278: 157-169. http://dx.doi.org/10.3354/meps278157
Tuya F., Boyra A., Sánchez-Jerez P., et al. 2005. Multivariate analysis of the bentho-demersal ichthyofauna along soft bottoms of the Eastern Atlantic: comparison between unvegetated substrates, seagrass meadows and sandy bottoms beneath sea-cage fish farms. Mar. Biol. 147: 1229-1237. http://dx.doi.org/10.1007/s00227-005-0018-1
Tuya F., Martín J.A., Luque A. 2006. Seasonal cycle of a Cymodocea nodosa seagrass meadow and of the associated ichthyofauna at Playa Dorada (Lanzarote, Canary Islands, eastern Atlantic). Cienc. Mar. 32: 695-704.
Tuya F., Wernberg T., Thomsen M.S. 2011. The relative influence of local to regional drivers of variation in reef fishes. J. Fish Biol. 79: 217-234. http://dx.doi.org/10.1111/j.1095-8649.2011.03015.x PMid:21722121
Tuya F., Ribeiro-Leite L., Arto-Cuesta N., et al. 2014a. Decadal changes in the structure of Cymodocea nodosa seagrass meadows: Natural vs. human influences. Estuar. Coast. Shelf Sci. 137: 41-49. http://dx.doi.org/10.1016/j.ecss.2013.11.026
Tuya F., Png-González L., Riera R., et al. 2014b. Ecological structure and function differs between habitats dominated by seagrasses and green seaweeds. Mar. Environ. Res. 98: 1-13. http://dx.doi.org/10.1016/j.marenvres.2014.03.015 PMid:24836641
Underwood A.J. 1997. Experiments in ecology. Their logical design and interpretation using analysis of variance. Cambridge University Press, 504 pp.
Published
How to Cite
Issue
Section
License
Copyright (c) 2015 Consejo Superior de Investigaciones Científicas (CSIC)

This work is licensed under a Creative Commons Attribution 4.0 International License.
© CSIC. Manuscripts published in both the print and online versions of this journal are the property of the Consejo Superior de Investigaciones Científicas, and quoting this source is a requirement for any partial or full reproduction.
All contents of this electronic edition, except where otherwise noted, are distributed under a Creative Commons Attribution 4.0 International (CC BY 4.0) licence. You may read here the basic information and the legal text of the licence. The indication of the CC BY 4.0 licence must be expressly stated in this way when necessary.
Self-archiving in repositories, personal webpages or similar, of any version other than the final version of the work produced by the publisher, is not allowed.