Marine Biology

, Volume 149, Issue 2, pp 149–167 | Cite as

Structure of a Mediterranean cryptobenthic fish community and its relationships with habitat characteristics

Research Article

Abstract

In the last 10 years, several studies have been carried out on the fish fauna of the Ustica Island marine reserve, yet no investigation was specifically addressed to the cryptobenthic fish assemblage. The first task of this study, conducted along the shallow rocky reefs of Ustica, was to determine the species composition, diversity and relative density of the resident cryptobenthic fishes. Furthermore, we aimed to assess the effects of some macro- and microscale habitat characteristics on the distribution pattern of fishes. In particular, the effect of predator density was indirectly evaluated by comparing density data collected within and outside the integral reserve zone. Overall, 20 species belonging to Blenniidae, Gobiidae, Tripterygiidae, Scorpaenidae and Gobiesocidae were recorded. Gobius bucchichi, Scorpaena maderensis, Tripterygion delaisi, T. melanurus and T. tripteronotus were the numerically dominant and most common species. The effects of zone (i.e. of predator density), bottom type and depth on species richness, diversity and evenness were not significant. A greater total fish density was observed on stones compared with rocky cliff and plateau, but only in the shallowest depth range. At level of single species, G. bucchichi was more abundant inside than outside the integral reserve, but only on stones and at 0–2 m depth range. Density of G. bucchichi was generally higher on stones than on rocky cliffs or plateau and between 0 and 5 m depth, although these differences were not always significant. T. delaisi was conversely more abundant in the deepest stratum (7–10 m). Canonical analyses demonstrated that bottom type and depth influenced significantly the fish assemblage structure. The observed differences in the assemblage structure relied mainly upon the dominant species. T. tripteronotus was mainly associated with rocky plateau and the intermediate depth range (3–5 m), whereas S. maderensis, T. melanurus and Lipophrys trigloides inhabited preferentially the rocky cliffs. At microscale level, the habitat choice of the investigated species was almost entirely based on whether the substrate was either vegetated or composed of bare rock. T. delaisi and T. tripteronotus were associated with substrata covered by algae, whilst G. bucchichi, S. maderensis and T. melanurus preferred bare rock bottoms. In some species, the electivity indices for the less abundant type of cover, measured at different spatial scale, changed accordingly. For instance, the smaller the size of the sampled area, the higher was the intensity of the association between G. bucchichi and Anemonia viridis.

References

  1. Abel EF (1960) Liaison facultative d’un poisson (Gobius bucchichii Steindachner) et d’une anémone (Anemonia sulcata Penn) en Méditerranée. Vie Milieu 11:517–531Google Scholar
  2. Abel EF (1962) Freiwasserbeobachtungen an Fischen im Golf von Neapel als Beitrag zur Kenntnis ihrer Ökologie und ihres Verhaltens. Int Rev Gesamten Hydrobiol 47:219–290CrossRefGoogle Scholar
  3. Ackerman JL, Bellwood DR (2000) Reef fish assemblages: a re-evaluation using enclosed rotenone stations. Mar Ecol Prog Ser 206:227–237CrossRefGoogle Scholar
  4. Anderson MJ (2003) CAP: a FORTRAN computer program for canonical analysis of principal coordinates. Department of Statistics, University of Auckland, New ZealandGoogle Scholar
  5. Anderson MJ, Willis TJ (2003) Canonical analysis of principal coordinates: a useful method of constrained ordination for ecology. Ecology 84:511–525CrossRefGoogle Scholar
  6. Arculeo M, Mazzola A, Parrinello N, Gristina M (1996) Dati sulla pesca costiera nell’Isola di Ustica (Tirreno meridionale). Nat Sicil Ser IV 20:109–118Google Scholar
  7. Bell JD (1983) Effects of depth and marine reserve fishing restrictions on the structure of a rocky reef fish assemblage in the north-western Mediterranean Sea. J Appl Ecol 20:357–369CrossRefGoogle Scholar
  8. Bellwood DR, Alcala AC (1988) The effect of a minimum length specification on visual estimates of density and biomass of coral reef fishes. Coral reefs 7:23–27CrossRefGoogle Scholar
  9. Benzecri JP, Benzecri F (1976) Pratique de l’analyse des données I: analyse des correspondance, exposé élémentaire. Dunod, ParisGoogle Scholar
  10. Brock RE (1982) A critique of the visual census method for assessing coral reef fish populations. Bull Mar Sci 32:269–276Google Scholar
  11. Caley MJ (1993) Predation, recruitment and the dynamics of communities of coral reef fishes. Mar Biol 117:33–43CrossRefGoogle Scholar
  12. Caley MJ, St John J (1996) Refuge availability structures assemblages of tropical reef fishes. J Anim Ecol 65:414–428CrossRefGoogle Scholar
  13. Carr MH (1991) Habitat selection and recruitment of an assemblage of temperate zone reef fishes. J Exp Mar Biol Ecol 146:113–137CrossRefGoogle Scholar
  14. Chabanet P, Ralambondrainy H, Amanieu M, Faure G, Galzin R (1997) Relationships between coral reef substrata and fish. Coral reefs 16:93–102CrossRefGoogle Scholar
  15. Connell SD, Jones GP (1991) The influence of habitat complexity on postrecruitment processes in a temperate reef fish population. J Exp Mar Biol Ecol 151:271–294CrossRefGoogle Scholar
  16. Costello MJ (1992) Abundance and spatial overlap of gobies (Gobiidae) in Lough Hyne, Ireland. Environ Biol Fish 33:239–248CrossRefGoogle Scholar
  17. Depczynski M, Bellwood DR (2003) The role of cryptobenthic fishes in coral reef trophodynamics. Mar Ecol Prog Ser 256:183–191CrossRefGoogle Scholar
  18. Ferreira CEL, Gonçalves JEA, Coutinho R (2001) Community structure of fishes and habitat complexity on a tropical rocky shore. Environ Biol Fish 61:353–369CrossRefGoogle Scholar
  19. García Charton JA, Pérez Ruzafa A (1998) Correlation between habitat structure and a rocky reef fish assemblage in the Southwest Mediterranean. Mar Ecol 19:111–128CrossRefGoogle Scholar
  20. García Charton JA, Pérez Ruzafa A (2001) Spatial pattern and the habitat structure of a Mediterranean rocky reef fish local assemblage. Mar Biol 138:917–934CrossRefGoogle Scholar
  21. Gibson RN (1969) The biology and behaviour of littoral fish. Oceanogr Mar Biol Annu Rev 7:367–410Google Scholar
  22. Gibson RN (1982) Recent studies on the biology of intertidal fishes. Oceanogr Mar Biol Annu Rev 20:363–414Google Scholar
  23. Gordina AD, Duka LA, Oven LS (1972) Sexual dimorphism, feeding and spawning in the black-headed blenny (Tripterygion tripteronotus Risso) of the Black Sea. J Ichthyol 12:401–407Google Scholar
  24. Gratwicke B, Speight MR (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. DOI 10.1111/j.1095-8649.2005.00629.xGoogle Scholar
  25. Greenacre M (1984) Theory and applications of correspondence analysis. Academic, New YorkGoogle Scholar
  26. Harmelin-Vivien M, Harmelin JG, Chauvet C, Duval C, Galzin R, Lejeune P, Barnabé G, Blanc F, Chevalier R, Duclerc J, Lassere G (1985) Evaluation visuelle des peuplements et populations de poissons: méthodes et problèmes. Rev Ecol Terr Vie 40:467–539Google Scholar
  27. Harmelin-Vivien ML, Kaim-Malka RA, Ledoyer M, Jacob-Abraham SS (1989) Food partitioning among scorpaenid fishes in Mediterranean seagrass beds. J Fish Biol 34:715–734CrossRefGoogle Scholar
  28. Heymer A, Zander CD (1975) Morphologische und Ökologische untersuchungen an Blennius rouxi, Cocco 1833 (Pisces, Perciformes, Blenniidae). Vie Milieu 25:311–333Google Scholar
  29. Hindell JS, Jenkins GP, Keough MJ (2000) Evaluating the impact of predation by fish on the assemblage structure of fishes, associated with seagrass (Heterozostera tasmanica) (Martens ex Ascherson) de Hartof, and unvegetated sand habitats. J Exp Mar Biol Ecol 255:153–174PubMedCrossRefGoogle Scholar
  30. Hixon MA, Beets JP (1993) Predation, prey refuges, and the structure of coral-reef fish assemblages. Ecol Monogr 63:77–101CrossRefGoogle Scholar
  31. Hixon MA, Carr MH (1997) Synergistic predation, density dependence, and population regulation in marine fish. Science 277:946–949CrossRefGoogle Scholar
  32. Hofrichter R, Patzner R (2000) Habitat and microhabitat of Mediterranean clingfishes (Teleostei: Gobiesociformes: Gobiesocidae). Mar Ecol 21:41–53CrossRefGoogle Scholar
  33. Illich IP, Kotrschal K (1990) Depth distribution and abundance of northern Adriatic littoral rocky reef blennioid fishes (Blenniidae and Tripterygion). Mar Ecol 11:277–289CrossRefGoogle Scholar
  34. Jacobs J (1974) Quantitative measurement of food selection, a modification of the forage ratio and Ivlev’s electivity index. Oecologia 14:413–417CrossRefGoogle Scholar
  35. Jennings S, Polunin NVC (1997) Impacts of predator depletion by fishing on the biomass and diversity of non-target reef fish communities. Coral Reefs 16:71–82CrossRefGoogle Scholar
  36. Jones GP (1991) Postrecruitment processes in the ecology of coral reef fish populations: a multifactorial perspective. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic, New York, pp 294–327Google Scholar
  37. Koppel VH (1988) Habitat selection and space partitioning among two Mediterranean Blenniid species. Mar Ecol 9:329–346CrossRefGoogle Scholar
  38. Kotrschal K (1983) Northern Adriatic rocky reef fishes at low winter temperatures. Mar Ecol 4:275–286CrossRefGoogle Scholar
  39. La Mesa G, Vacchi M (1999) The coastal fishes of the Ustica Island marine reserve (Mediterranean Sea): pluriannual surveys by visual census. Mar Ecol 20:147–165CrossRefGoogle Scholar
  40. La Mesa G, Vacchi M (2005) Analysis of the blennioid assemblages associated with different rocky shores habitats in the Ligurian Sea (northwestern Mediterranean). J Fish Biol 66:1300–1327. DOI 10.1111/j.1095-8649.2005.00684.xGoogle Scholar
  41. La Mesa G, Micalizzi M, Giaccone G, Vacchi M (2004) Cryptobenthic fishes of the “Ciclopi Islands” marine reserve (Central Mediterranean Sea): assemblage composition, structure and relations with habitat features. Mar Biol 145:233–242. DOI 10.1007/s00227-004-1315-9Google Scholar
  42. Levin PS, Hay ME (1996) Responses of temperate reef fishes to alterations in algal structure and species composition. Mar Ecol Prog Ser 134:37–47CrossRefGoogle Scholar
  43. Lincoln Smith MP (1988) Effects of observer swimming speed on sample counts of temperate rocky reef fish assemblages. Mar Ecol Prog Ser 43:223–231CrossRefGoogle Scholar
  44. Luckhurst BE, Luckhurst K (1978) Analysis of the influence of substrate variables on coral reef fish communities. Mar Biol 49:317–323CrossRefGoogle Scholar
  45. Macpherson E (1994) Substrate utilisation in a Mediterranean littoral fish community. Mar Ecol Prog Ser 114:211–218CrossRefGoogle Scholar
  46. Macpherson E, Zika U (1999) Temporal and spatial variability of settlement success and recruitment level in three blennoid fishes in the northwestern Mediterranean. Mar Ecol Prog Ser 182:269–282CrossRefGoogle Scholar
  47. Mcgehee MA (1994) Correspondence between assemblages of coral reef fishes and gradients of water motion, depth, and substrate size off Puerto Rico. Mar Ecol Prog Ser 105:243–255CrossRefGoogle Scholar
  48. Miller PJ (1979) Adaptiveness and implications of small size in Teleosts. Symp Zool Soc Lond 44:263–306Google Scholar
  49. Miller PJ (1986) Gobiidae. In: Whitehead PJP, Bauchot ML, Hureau JC, Nielsen J, Tortonese E (eds) Fishes of the North-eastern Atlantic and the Mediterranean. UNESCO, Paris, pp 1096–1112Google Scholar
  50. Nieder J, La Mesa G, Vacchi M (2000) Blenniidae along the Italian coasts of the Ligurian and the Tyrrhenian sea: community structure and new records of Scartella cristata for northern Italy. Cybium 24:359–369Google Scholar
  51. Ohman MC, Rajasuriya A (1998) Relationships between habitat structure and fish communities on coral and sandstone reefs. Environ Biol Fish 53:19–31CrossRefGoogle Scholar
  52. Patzner RA (1999) Habitat utilization and depth distribution of small cryptobenthic fishes (Blennidae, Gobiesocidae, Gobiidae, Tripterygiidae) in Ibiza (western Mediterranean Sea). Environ Biol Fish 55:207–214CrossRefGoogle Scholar
  53. Pielou EC (1966) The measurement of diversity in different types of biological collections. J Theor Biol 13:131–144CrossRefGoogle Scholar
  54. Prochazka K (1998) Spatial and trophic partitioning in cryptic fish communities of shallow subtidal reefs in False Bay, South Africa. Environ Biol Fish 51:201–220CrossRefGoogle Scholar
  55. Roberts CM, Ormond RFG (1987) Habitat complexity and coral reef fish diversity and abundance on Red Sea fringing reefs. Mar Ecol Prog Ser 41:1–8CrossRefGoogle Scholar
  56. Sasal P, Faliex E, Morand S (1996) Population structure of Gobius bucchichii in a Mediterranean marine reserve and in an unprotected area. J Fish Biol 49:352–356Google Scholar
  57. Syms C (1995) Multi-scale analysis of habitat association in a guild of blennioid fishes. Mar Ecol Prog Ser 125:31–43CrossRefGoogle Scholar
  58. Syms C, Jones GP (1999) Scale of disturbance and the structure of a temperate fish guild. Ecology 80:921–940CrossRefGoogle Scholar
  59. Thompson S (1983) Homing in a territorial reef fish. Copeia 1983:832–834CrossRefGoogle Scholar
  60. Tupper M, Boutilier RG (1997) Effects of habitat on settlement, growth, predation risk and survival of a temperate reef fish. Mar Ecol Prog Ser 151:225–236CrossRefGoogle Scholar
  61. Underwood AJ (1981) Techniques of analysis of variance in experimental marine biology and ecology. Oceanogr Mar Biol Annu Rev 19:513–605Google Scholar
  62. Underwood AJ (1997) Experiments in ecology: their logical design and interpretation using analysis of variance. Cambridge University Press, CambridgeGoogle Scholar
  63. Vacchi M, Boyer M, Bussotti S, Guidetti P, La Mesa G (1999a) Some interesting species in the coastal fish fauna of Ustica Island (Mediterranean Sea). Cybium 23:323–331Google Scholar
  64. Vacchi M, Bussotti S, Guidetti P, La Mesa G (1999b) Osservazioni preliminari sulle cernie della Riserva Marina di Ustica (Tirreno Meridionale, Mar Mediterraneo). Biol Mar Med 6:278–280Google Scholar
  65. Vacchi M, La Mesa G, Finoia MG, Guidetti P, Bussotti S (1999c) Protection measures and juveniles of dusky grouper Epinephelus marginatus (Lowe, 1834) (Pisces, Serranidae) in the marine reserve of Ustica Island (Italy, Mediterranean Sea). Mar Life 9:63–70Google Scholar
  66. Wilkins HKA, Myers AA (1992) Microhabitat utilisation by an assemblage of temperate Gobiidae (Pisces: Teleostei). Mar Ecol Prog Ser 90:103–112CrossRefGoogle Scholar
  67. Willis TJ (2001) Visual census methods underestimate density and diversity of cryptic reef fishes. J Fish Biol 59:1408–1411CrossRefGoogle Scholar
  68. Willis TJ, Anderson MJ (2003) Structure of cryptic reef fish assemblages: relationships with habitat characteristics and predator density. Mar Ecol Prog Ser 257:209–221CrossRefGoogle Scholar
  69. Zander CD (1972) Beiträge zur Ökologie und Biologie von Blenniidae (Pisces) des Mittelmeeres. Helgol Meeresunters 23:193–231CrossRefGoogle Scholar
  70. Zander CD (1986) Blenniidae. In: Whitehead PJP, Bauchot ML, Hureau JC, Nielsen J, Tortonese E (eds) Fishes of the north-eastern Atlantic and the Mediterranean. UNESCO, Paris, pp 1096–1112Google Scholar
  71. Zander CD, Hagemann T (1989) Feeding ecology of littoral gobiid and blennioid fishes of the Banyuls area (Mediterranean Sea): 3. Seasonal variations. In: Ros J (ed) Topics in Marine Biology. Sci Mar 53(2–3):441–449Google Scholar
  72. Zander CD, Heymer A (1970) Tripterygion tripteronotus (Risso, 1810) und Tripterygion xanthosoma n. sp.—eine ökologische Speziation (Pisces, Teleostei). Vie Milieu 21A:363–394Google Scholar
  73. Zander CD, Heymer A (1976) Morphologische und ökologische Untersuchungen an den speleophilen Schleimfischartigen Tripterygion melanurus Guichenot, 1850 und T. minor Kolombatovic, 1892 (Perciformes, Blennioidei, Tripterygiidae). Z Zool Syst Evol For 14:41–59Google Scholar
  74. Zander CD, Heymer A (1977) Analysis of ecological equivalents among littoral fishes. In: Keegan BF, Ceidigh PO, Boaden PJS (eds) Biology of benthic organisms. Pergamon Press, Oxford, pp 621–630Google Scholar

Copyright information

© Springer-Verlag 2005

Authors and Affiliations

  1. 1.ICRAM, Istituto Centrale per la Ricerca Applicata al MareRomeItaly

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