Hostname: page-component-848d4c4894-p2v8j Total loading time: 0.001 Render date: 2024-06-02T08:46:52.349Z Has data issue: false hasContentIssue false
  • English
  • Français

Pelagic larval duration, size at settlement and coastal recruitment of the intertidal blenny Lipophrys pholis

Published online by Cambridge University Press:  13 January 2016

Margarida G. Carvalho ,
Cláudia Moreira ,
Henrique Queiroga ,
Paulo T. Santos  and
Alberto T. Correia
Margarida G. Carvalho
Affiliation:
Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR/CIMAR), Rua dos Bragas 289, 4050-123 Porto, Portugal Faculdade de Ciências daUniversidade do Porto (FCUP), Rua Campo Alegre 1021/1055, 4169-007 Porto, Portugal
Cláudia Moreira
Affiliation:
Faculdade de Ciências daUniversidade do Porto (FCUP), Rua Campo Alegre 1021/1055, 4169-007 Porto, Portugal
Henrique Queiroga
Affiliation:
Centro de Estudos do Ambiente e do Mar da Universidade de Aveiro (CESAM), Campus Universitário de Santiago, 3810-193 Aveiro, Portugal
Paulo T. Santos
Affiliation:
Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR/CIMAR), Rua dos Bragas 289, 4050-123 Porto, Portugal Faculdade de Ciências daUniversidade do Porto (FCUP), Rua Campo Alegre 1021/1055, 4169-007 Porto, Portugal
Alberto T. Correia*
Affiliation:
Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR/CIMAR), Rua dos Bragas 289, 4050-123 Porto, Portugal Faculdade de Ciências da Saúde da Universidade Fernando Pessoa (FCS/UFP), Rua Carlos Maia 296, 4200-150 Porto, Portugal
*
Correspondence should be addressed to:A.T. Correia, Centro Interdisciplinar de Investigacão Marinha e Ambiental (CIIMAR/CIMAR), Rua dos Bragas 289, 4050-123 Porto, Portugal email: atcorreia.ciimar@gmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

To study some early life history traits of Lipophrys pholis, 110 recruits (TL ≤ 30 mm) were collected in April and May 2013 during the low tide periods in four rocky beaches along the west (Cabo do Mundo, Peniche and Vale do Homem) and south (Olhos de Água) Portuguese coasts. Pelagic larval duration, size at settlement and age at coastal recruitment were back-calculated from the microstructure of otoliths. Pelagic larval duration estimated from micro-increment counts until the settlement marks ranged from 57 to 73 days and showed a latitudinal reduction trend from north to south. This variable seems to be related in 30% with the regional seawater temperatures probably through the direct effect on the somatic growth. Settlement sizes (~19 mm) did not show any regional differences suggesting that this is a more conservative character within species. The mean age at coastal recruitment varied between 69 and 93 days, but northern individuals were recruited at an older age. Back-calculated spawning, hatching and settlement dates appear to be unrelated to the lunar cycle for L. pholis.

Keywords

Blenniessagittaemicro-incrementsearly life history
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 97 , Issue 1 , February 2017 , pp. 197 - 205
Copyright
Copyright © Marine Biological Association of the United Kingdom 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Almada, V.C., Barata, E.N., Gonçalves, E.J. and Oliveira, R.F. (1990) On the breeding season of Lipophrys polis (Pisces: Blennidae) at Arrábida, Portugal. Journal of the Marine Biological Association of the United Kingdom 70, 913–916.CrossRefGoogle Scholar
Almada, V.C., Oliveira, R.F., Gonçalves, E.J., Almeida, A.J., Santos, R.S. and Wirtz, P. (2001) Patterns of diversity of the north-eastern Atlantic blenniid fish fauna (Pisces: Blenniidae). Global Ecology and Biogeography 10, 411–422.CrossRefGoogle Scholar
Atkinson, D. (1996) Ectotherm life-history responses to developmental temperature. In Johnston, I.A. and Bennett, A.F. (eds) Animals and temperature: phenotypic and evolutionary adaptation. Cambridge: Cambridge University Press, pp. 183–205.Google Scholar
Batschelet, E. (1981) Circular statistics in biology. London: Academic Press, 371 pp.Google Scholar
Baumann, H., Hinrichsen, H.H., Voss, R., Stepputtis, D., Grygiel, W., Clausen, L.W. and Temming, A. (2006) Linking growth to environmental histories in central Baltic young-of-the-year sprat, Sprattus sprattus: an approach based on otolith microstructure analysis and hydrodynamic modeling. Fisheries Oceanography 15, 465–476.Google Scholar
Beldade, R., Pedro, T. and Gonçalves, J. (2007) Pelagic larval duration of 10 temperate cryptobenthic fishes. Journal of Fish Biology 71, 376–382.CrossRefGoogle Scholar
Benoît, H.P., Pepin, P. and Brown, J.A. (2000) Patterns of metamorphic age and length in marine fishes, from individuals to taxa. Canadian Journal of Fisheries and Aquatic Sciences 57, 856–869.CrossRefGoogle Scholar
Campana, S.E. and Neilson, J. (1985) Microstructure of fish otoliths. Canadian Journal of Fisheries and Aquatic Sciences 42, 1014–1032.CrossRefGoogle Scholar
Carr, M. and Sims, C. (2006) Recruitment. In Allen, L.G., Pondella, D.J. and Horn, M.H. (eds) The ecology of marine fishes: California and adjacent waters. Berkeley, CA: University of California Press, pp. 411–427.Google Scholar
Carvalho, M.G., Moreira, A.S., Moreira, C., Queiroga, H., Santos, P.T. and Correia, A.T. (2014) Validation of otolith daily increments in early juveniles of shanny Lipophrys pholis . Journal of Fish Biology 84, 1234–1239.CrossRefGoogle ScholarPubMed
Carvalho, M.G., Moreira, A.S., Moreira, C., Queiroga, H., Santos, P.T. and Correia, A.T. (2015) Ontogenetic development of the sagittal otoliths of Lipophrys pholis (Blenniidae) during the embryonic, larval and settlement stages. Ichthyological Research 62, 351–356.Google Scholar
Chambers, R.C. and Leggett, W.C. (1987) Size and age at metamorphosis in marine fishes: an analysis of laboratory-reared winter flounder (Pseudopleuronectes americanus) with a review of variation in other species. Canadian Journal of Fisheries Aquatic Sciences 44, 1936–1947.Google Scholar
Conover, D.O. (1992) Seasonality and the scheduling of life history at different latitudes. Journal of Fish Biology 41, 161–178.CrossRefGoogle Scholar
Dunne, J. (1977) Littoral and benthic investigations on the West coast of Ireland – VII. (Section A: faunistic and ecological studies). The biology of the shanny, Blennius pholis L. (Pisces) at Carna, Connemara. Proceedings of the Royal Irish Academy 77, 207–226.Google Scholar
Faria, C. and Almada, V.C. (2001) Agonistic behaviour and control of access to hiding places in two intertidal blennies, Lipophrys pholis and Coryphoblennius galerita (Pisces: Blenniidae). Acta Ethologica 4, 51–58.CrossRefGoogle Scholar
Faria, C., Almada, V.C. and Gonçalves, E.J. (1996) Juvenile recruitment, growth and maturation of Lipophrys pholis (Pisces: Blenniidae), from the west coast of Portugal. Journal of Fish Biology 49, 727–730.Google Scholar
Faria, C., Borges, R., Gil, F., Almada, V.C. and Gonçalves, E. (2002) Embryonic and larval development of Lipophrys pholis (Pisces: Blenniidae). Scientia Marina 66, 21–26.CrossRefGoogle Scholar
Ferreira, F., Santos, M.M., Reis-Henriques, M.A., Vieira, N. and Monteiro, N. (2011) The annual cycle of spermatogenesis in Lipophrys pholis (Blenniidae), a recently proposed sentinel species for pollution monitoring. Ichthyological Research 58, 360–365.CrossRefGoogle Scholar
Ferreira, F., Santos, M.M., Reis-Henriques, M.A., Vieira, N. and Monteiro, N. (2012) The annual cycle of oogenesis in the shanny Lipophrys pholis (Pisces: Blennidae). Scientia Marina 76, 273–280.Google Scholar
Green, B.S. and Fisher, R. (2004) Temperature influences swimming speed, growth and larval duration in coral reef fish larvae. Journal of Experimental Marine Biology and Ecology 299, 115–132.Google Scholar
Green, B.S., Mapstone, B.D., Carlos, G. and Begg, G.A. (ed.) (2009) Tropical fish otoliths: information for assessment, management and ecology. New York, NY: Springer Science plus Business Media, pp. 1571–3075.Google Scholar
Jones, G.P. (1986) Food availability affects growth in a coral reef fish. Oecologia 70, 136–139.Google Scholar
Jorge, P.E., Almada, F., Gonçalves, A.R., Duarte-Coelho, P. and Almada, V.C. (2012) Homing in rocky intertidal fish. Are Lipophrys pholis able to perform true navigation? Animal Cognition 15, 1173–1181.Google Scholar
Juncker, M., Wantiez, L. and Ponto, D. (2006) Flexibility in size and age at settlement of coral reef fish: spatial and temporal variations in Wallis Islands (South Central Pacific). Aquatic Living Resources 19, 339–348.Google Scholar
Kendall, M.S., Poti, M., Wynne, T.T., Kinlan, B.P. and Bauer, L.B. (2013) Consequences of the life history traits of pelagic larvae on interisland connectivity during a changing climate. Marine Ecology Progress Series 489, 43–59.Google Scholar
Lemos, R.T. and Sansó, B. (2006) Spatio-temporal variability of ocean temperature in the Portugal Current System. Journal of Geophysical Research 111, C04010.Google Scholar
Lobel, P.S. and Robinson, A.R. (1986) Transport and entrapment of fish larvae by ocean mesoscale eddies and currents in Hawaiian waters. Deep-Sea Research 33, 483–500.Google Scholar
Maillet, G.L. and Checkley, D.M. Jr (1991) Storm-related variation in the growth rate of otoliths of larval Atlantic menhaden, Brevoortia tyrannus: a time series analysis of biological and physical variables and implications for larva growth and mortality. Marine Ecology Progress Series 79, 1–16.Google Scholar
Marliave, J.B. (1986) Lack of planktonic dispersal of rocky intertidal fish larvae. Transactions of the American Fisheries Society 115, 149–154.Google Scholar
May, H.M.A. and Jenkins, G.P. (1992) Patterns of settlement and growth of juvenile flounder Rhombosolea tapirina determined from otolith microstructure. Marine Ecology Progress Series 79, 203–214.Google Scholar
McCormick, M.I. (1994) Variability in age and size at settlement of the tropical goatfish Upeneus tragula (Mullidae) in the Great Barrier Reef lagoon. Marine Ecology Progress Series 103, 1–15.Google Scholar
McCormick, M.I. (1999) Delayed metamorphosis of a tropical reef fish (Acanthurus triostegus): a field experiment. Marine Ecology Progress Series 176, 25–38.CrossRefGoogle Scholar
McCormick, M.I. and Molony, B.W. (1995) Influence of water temperature during the larval stage on size, age and body condition of a tropical reef fish at settlement. Marine Ecology Progress Series 118, 59–68.Google Scholar
Meekan, M.G., Carleton, J.H., McKinnon, A.D., Flynn, K. and Furnas, M. (2003) What determines the growth of tropical reef fish larvae in the plankton: food or temperature? Marine Ecology Progress Series 256, 193–204.Google Scholar
Milton, P. (1983) Biology of littoral blenniid fishes on the coast of South-West England. Journal of the Marine Biological Association of the United Kingdom 63, 223–237.CrossRefGoogle Scholar
Morales-Nin, B. (2000) Review of the growth regulation process of otolith daily increment formation. Fisheries Research 46, 53–67.CrossRefGoogle Scholar
Morrongiello, J.R., Bond, N.R., Crook, D.A. and Wong, B.B. (2012) Spatial variation in egg size and egg number reflects trade-offs and bet-hedging in a freshwater fish. Journal of Animal Ecology 81, 806–817.CrossRefGoogle Scholar
Pastén, G.P., Katayama, S. and Omori, M. (2003) Timing of parturition, planktonic duration, and settlement patterns of the black rockfish, Sebastes inermis . Environmental Biology of Fishes 68, 229–239.Google Scholar
Qasim, S.Z. (1957) The biology of Blenniius pholis L. (Teleostei). Proceedings of the Zoological Society of London 128, 161–206.Google Scholar
Radtke, R.L., Kinzie, R.A. and Shaffer, D.J. (2001) Temporal and spatial variation in length of larval life and size at settlement of the Hawaiian amphidromous goby Lentipes concolor . Journal of Fish Biology 59, 928–938.Google Scholar
Raventós, N. and Macpherson, E. (2001) Planktonic larval duration and settlement marks on the otoliths of Mediterranean littoral fishes. Marine Biology 138, 1115–1120.Google Scholar
Robertson, D.R., Petersen, C.N. and Brawn, J.D. (1990) Lunar reproductive cycles of benthic-brooding reef fishes: reflections of larval biology or adult biology? Ecological Monographs 60, 311–321.Google Scholar
Searcy, S. and Sponaugle, S. (2001) Selective mortality during the larval – juvenile transition in two coral reef fishes. Ecology 82, 2452–2470.Google Scholar
Sponaugle, S. (2010) Otolith microstructure reveals ecological and oceanographic processes important to ecosystem-based management. Environmental Biology of Fishes 89, 221–238.Google Scholar
Sponaugle, S. and Cowen, R.K. (1994) Larval duration and recruitment patterns of two Caribbean gobies (Gobiidae), contrasting early life histories in demersal spawners. Marine Biology 120, 133–144.Google Scholar
Sponaugle, S., Grorud-Colvert, K. and Pinkard, D. (2006) Temperature-mediated variation early life history traits and recruitment success of the coral reef fish Thalassoma bifasciatum in the Florida Keys. Marine Ecological Progress Series 308, 1–15.Google Scholar
Sponaugle, S. and Pinkard, D.R. (2004) Lunar cyclic population replenishment of a coral reef fish: shifting patterns following oceanic events. Marine Ecological Progress Series 267, 267–280.Google Scholar
Takemura, A., Rahman, M.S. and Park, Y.J. (2010) External and internal controls of lunar-related reproductive rhythms in fishes. Journal of Fish Biology 76, 7–26.Google Scholar
Wilson, D.T. and McCormick, M.I. (1999) Microstructure of settlement marks in the otoliths of tropical reef fishes. Marine Biology 134, 29–41.Google Scholar
Zander, C. (1986) Blenniidae. In Whitehead, P., Bauchot, M.L., Hureau, J.C., Nielsen, J. and Tortonese, E. (eds) Fishes of the Northeastern Atlantic and the Mediterranean. Paris: UNESCO, pp. 1096–1112.Google Scholar
Zar, J.H. (1996) Biostatistical analysis, 3rd edition. London: Prentice-Hall.Google Scholar