A preliminary assessment of larval fish assemblages on artificial reefs in the nearshore Southern Brazil
DOI:
https://doi.org/10.1590/2675-2824069.21-002cba%20Keywords:
Fish egg, Fish larvae, Light trap, Exotic species, Ecological successionAbstract
Artificial reefs (ARs) have been deployed on the inner shelf of Paraná, Southeast Brazil, as protection against destructive trawling activities, and to offer habitat for local fauna for recovery of biodiversity. The purpose of this study was to develop a preliminary characterization of the ichthyoplankton community associated with both artificial and natural reefs in the Currais Archipelago, and perform a comparison of fish larvae composition between ARs and nearby unconsolidated substrate. Two sampling methods were used, light traps and a plankton net. A total of 12 families and 14 species were identified, expanding the total species list in the area by eight species and three families. Differences among assemblages on ARs and unconsolidated substrate indicate that ARs seem to be effective attractors to fish larvae. Particular attention is drawn in regard to the "attractor effect" for exotic species that do not naturally reside in the area, such as Omobranchus punctatus. The large abundance of fish eggs on ARs suggests that these artificial structures can improve local production. These results are the first step needed to better define guidelines for sustainable use and management of ARs and Currais Archipelago, a Marine National Park.
References
Airoldi, L., Turon, X., Perkol-Finkel, S. & Rius, M. 2015. Corridors for aliens but not for natives: effects of marine urban sprawl at a regional scale. Diversity and Distributions, 21(7), 755-768, DOI: https://doi.org/10.1111/ddi.12301
» https://doi.org/10.1111/ddi.12301
Anderson, M. J. 2008. A new method for non-parametric multivariate analysis of variance. Austral Ecology, 26(1), 32-46, DOI: https://doi.org/10.1111/j.1442-9993.2001.01070.pp.x
» https://doi.org/10.1111/j.1442-9993.2001.01070.pp.x
Andersson, M. H. & Öhman, M. C. 2010. Fish and sessile assemblages associated with wind-turbine constructions in the Baltic Sea. Marine and Freshwater Research, 61(6), 642-650, DOI: https://doi.org/10.1071/MF09117
» https://doi.org/10.1071/MF09117
Anderson, M. J. & Willis, T. J. 2003. Canonical analysis of principal coordinates: a useful method of constrained ordination for ecology. Ecology, 84(2), 511-525, DOI: https://doi.org/10.1890/0012-9658(2003)084[0511:CAOPCA]2.0.CO;2
» https://doi.org/10.1890/0012-9658(2003)084[0511:CAOPCA]2.0.CO;2
Andriguetto-Filho, J. M. & Pierri, N. 2012. Participation of small-scale fishermen in the design of a project for creating artificial reefs in the south of Brazil. CUHSO, 22(1), 95-113.
Arvedlund, M. & Kavanagh, K. 2009. The senses and environmental cues used by marine larvae of fish and decapods crustaceans to find tropical coastal ecosystems. In: Nagelkerken, L. (ed.). Ecological connectivity among tropical coastal ecosystems Dordrecht: Springer.
Atema, J., Kingsford, M. J. & Gerlach, G. 2002. Larval fish could use odour for detection, retention and orientation to reefs. Marine Ecology Progress Series, 241, 151-160, DOI: https://doi.org/10.3354/meps241151
» https://doi.org/10.3354/meps241151
Batty, R. S. & Hoyt, R. D. 1995. The role of sense organs in the feeding behaviour of juvenile sole and plaice. Journal of Fish Biology, 47(6), 931-939, DOI: https://doi.org/10.1111/j.1095-8649.1995.tb06019.x
» https://doi.org/10.1111/j.1095-8649.1995.tb06019.x
Beckerman, A., Benton, T. G., Ranta, E., Kaitala, V. & Lundberg, P. 2002. Population dynamic consequences of delayed life-history effects. Trends in Ecology & Evolution, 17(6), 263-269, DOI: https://doi.org/10.1016/S0169-5347(02)02469-2
» https://doi.org/10.1016/S0169-5347(02)02469-2
Beldade, R., Borges, R. & Goncalves, E. J. 2006. Depth distribution of nearshore temperate fish larval assemblages near rocky substrates. Journal of Plankton Research, 28(11), 1003-1013, DOI: https://doi.org/10.1093/plankt/fbl035
» https://doi.org/10.1093/plankt/fbl035
Bellwood, D. R. 1998. What are reef fishes? - Comment on the report by Robertson, D.R.: Do coral-reef fish faunas have a distinctive taxonomic structure? Coral Reefs, 17, 187-189, DOI: https://doi.org/10.1007/s003380050114
» https://doi.org/10.1007/s003380050114
Bellwood, D. R. & Wainwright, P. C. 2002. The history and biogeography of fishes on coral reefs. In: Sale, P. S. (ed.). Coral reef fishes: dynamics and diversity in a complex ecosystem San Diego: Elsevier Science. pp. 5-32.
Ben-Tzvi, O., Tchernov, D. & Kiflawi, M. 2010. Role of coral-derived chemical cues in microhabitat selection by settling Chromis viridis. Marine Ecology Progress Series, 409, 181-187, DOI: https://doi.org/10.3354/meps08627
» https://doi.org/10.3354/meps08627
Borges, R., Beldade, R. & Gonçalves, E. J. 2007. Vertical structure of very nearshore larval fish assemblages in a temperate rocky coast. Marine Biology, 151(4), 1349-1363, DOI: https://doi.org/10.1007/s00227-006-0574-z
» https://doi.org/10.1007/s00227-006-0574-z
Brandini, F. P. 1990. Hydrography and characteristics of the phytoplankton in shelf and oceanic waters off southeastern Brazil during winter (July/August 1982) and summer (February/March 1984). Hydrobiologia, 196(2), 111-148, DOI: https://doi.org/10.1007/BF00006105
» https://doi.org/10.1007/BF00006105
Brandini, F. P. 2014. Marine biodiversity and sustainability of fishing resources in Brazil: a case study of the coast of Paraná state. Regional Environmental Change, 14, 2127-2137, DOI: https://doi.org/10.1007/s10113-013-0458-y
» https://doi.org/10.1007/s10113-013-0458-y
Brandini, F. & Silva, A. S. 2011. Epilithic community development on artificial reefs deployed along a cross-shelf environmental gradient off Paraná state, southern Brazil. Brazilian Journal of Oceanography, 59(spe1), 43-53.
Bohnsack, J. A. 1989. Are high densities of fishes at artificial reefs the result of habitat limitation or behavioural preference? Bulletin of Marine Science, 44(2), 631-645.
Bohnsack, J. A., Johnson, D. L. & Ambrose, R. F. 1991. Ecology of artificial reef habitats and fishes. In: Seaman, W. & Sprague, L. M. (eds.). Artificial habitats for marine and freshwater fisheries San Diego: Academic Press.
Brochier, T., Auger, P., Thiam, N., Sow, M., Diouf, S., Sloterdijk, H. & Brehmer, P. 2015. Implementation of artificial habitats: inside or outside the marine protected areas? Insights from a mathematical approach. Ecological Modelling, 297, 98-106, DOI: https://doi.org/10.1016/j.ecolmodel.2014.10.034
» https://doi.org/10.1016/j.ecolmodel.2014.10.034
Buri, P. & Kawamura, G. 1983. The mechanics of mass occurrence and recruitment strategy of milkfish Chanos chanos (Forsskål) fry in the Philippines. Kagoshima University Research Center for the Pacific Islands, 3(2), 33-55.
Caley, M. J., Carr, M. H., Hixon, M. A., Hughes, T. P., Jones, G. P. & Menge, B. A. 1996. Recruitment and the local dynamics of open marine populations. Annual Review of Ecology and Systematics, 27(1), 477-500, DOI: https://doi.org/10.1146/annurev.ecolsys.27.1.477
» https://doi.org/10.1146/annurev.ecolsys.27.1.477
CASTRO, B. D. & MIRANDA, L. D. 1998. Physical oceanography of the western Atlantic continental shelf located between 4 N and 34 S.The Sea, 11(1), 209-251.
Castro, B. M., Brandini, F. P., Pires-Vanin, A. M. S. & Miranda, L. B. 2006. Multidisciplinary oceanographic processes on the Western Atlantic continental shelf between 4 N and 34 S. The Sea, 11, 209-251.
Campos, J. A. & Gamboa, C. 1989. An artificial tire-reef in a tropical marine system: a management tool. Bulletin of Marine Science , 44(2), 757-766.
Castro, M. S. D., Bonecker, A. C. T. & Valentin, J. L. 2005. Seasonal variation in fish larvae at the entrance of Guanabara Bay, Brazil. Brazilian Archives of Biology and Technology, 48(1), 121-128, DOI: http://dx.doi.org/10.1590/S1516-89132005000100016
» http://dx.doi.org/10.1590/S1516-89132005000100016
Catalán, I. A., Dunand, A., Alvarez, I., Alós, J., Colinas, N. & Nash, R. D. 2014. An evaluation of sampling methodology for assessing settlement of temperate fish in seagrass meadows. Mediterranean Marrine Science, 15(2), 338-349, DOI: https://doi.org/10.12681/mms.539
» https://doi.org/10.12681/mms.539
Cervigón, F., Cipriani, R., Fischer, W., Garibaldi, L., Hendrickx, M., Lemus, A. J., Márquez, R., Poutiers, J. M., Robaina, G. & Rodriguez, B. 1992. Fichas FAO de identificación de especies para los fines de la pesca. Guía de campo de las especies comerciales marinas y de aquas salobres de la costa septentrional de Sur América Rome: FAO.
Choat, J. H. 1993. A comparison of towed nets, purse seine, and light-aggregation devices for sampling larvae and pelagic juveniles of coral reef fishes. Fishery Bulletin, 91(2), 195-209.
Clarke, K. R. 1993. Non-parametric multivariate analyses of changes in community structure. Australian Journal of Ecology , 18(1), 117-143, DOI: https://doi.org/10.1111/j.1442-9993.1993.tb00438.x
» https://doi.org/10.1111/j.1442-9993.1993.tb00438.x
Clarke, K. R. & Warwick, R. M. 2001. Change in marine communities: an approach to statistical analysis and interpretation 2 Plymouth: PRIMER-E Ltd.
Clutter, R. I. & Anraku, M. 1968. Avoidance of samplers. Zooplankton sampling, monographs on oceanographic methodology, 2, 57-76.
Contente, R. F., Brenha-Nunes, M. R., Siliprandi, C. C., Lamas, R. A & Conversani, V. R. M. 2015. Occurrence of the non-indigenous Omobranchus punctatus (Blenniidae) on the São Paulo coast, South-Eastern Brazil. Marine Biodiversity Records, 8(73), 1-4, DOI: https://doi.org/10.1017/S175526721500055X
» https://doi.org/10.1017/S175526721500055X
Costa, M. D. P., Souza-Conceição, J. M., Schwingel, P. R. & Spach, H. L. 2011. Assessment of larval distribution of invasive Omobranchus punctatus (Valenciennes, 1836) (Pisces: Blenniidae) in a subtropical estuary (Southern Brazil). Aquatic Invasions, 6(1), 33-38, DOI: https://doi.org/10.3391/ai.2011.6.S1.008
» https://doi.org/10.3391/ai.2011.6.S1.008
Côté, I. M. & Maljković, A. 2010. Predation rates of Indo-Pacific lionfish on Bahamian coral reefs. Marine Ecology Progress Series, 404, 219-225, DOI: https://doi.org/10.3354/meps08458
» https://doi.org/10.3354/meps08458
Cresson, P., Ruitton, S. & Harmelin-Vivien, M. 2014 Artificial reefs do increase secondary biomass production: mechanisms evidenced by stable isotopes. Marine Ecology Progress Series, 509, 15-26, DOI: https://doi.org/10.3354/meps10866
» https://doi.org/10.3354/meps10866
Cummings, S. L. 1994. Colonization of a nearshore artificial reef at Boca Ratón (Palm Beach county). Florida Bulletin of Marine Science , 55(2-3), 1193-1215.
Daros, F. A. L., Bueno, L. S., Soeth, M., Bertoncini, Á. A., Hostim-Silva, M. & Spach, H. L. 2018. Rocky reef fish assemblage structure in coastal islands of southern Brazil. Latin American Journal of Aquatic Research, 46(1), 197-211.
Daros, F. A. L., Bueno, L. S., Vilar, C. C., Passos, A. C. & Spach, H. L. 2012. Checklist of rocky reef fishes from the Currais Archipelago and Itacolomis Island, Paraná state, Brazil. Check List, 8(3), 349-354, DOI: http://dx.doi.org/10.15560/8.3.349
» http://dx.doi.org/10.15560/8.3.349
Daros, F. A. L., Spach, H. L., Sial, A. N. & Correia, A. T. 2016. Otolith fingerprints of the coral reef fish Stegastes fuscus in southeast Brazil: a useful tool for population and connectivity studies. Regional Studies in Marine Science, 3, 262-272, DOI: https://doi.org/10.1016/j.rsma.2015.11.012
» https://doi.org/10.1016/j.rsma.2015.11.012
Davis, N., VanBlaricom, G. R. & Dayton, P. K. 1982. Man-made structures on marine sediments: effects on adjacent benthic communities. Marine Biology , 70(3), 295-303, DOI: https://doi.org/10.1007/BF00396848
» https://doi.org/10.1007/BF00396848
DeMartini, E. E., Barnett, A. M., Johnson, T. D. & Ambrose, R. F. 1994. Growth and production estimates for biomass-dominant fishes on a southern California artificial reef. Bulletin of Marine Science , 55(2-3), 484-500.
De Roos, A. M., Persson, L. & McCauley, E. 2003. The influence of size-dependent life-history traits on the structure and dynamics of populations and communities. Ecology Letters, 6(5), 473-487, DOI: https://doi.org/10.1046/j.1461-0248.2003.00458.x
» https://doi.org/10.1046/j.1461-0248.2003.00458.x
Dixson, D. L., Munday, P. L. & Jones, G. P. 2010. Ocean acidification disrupts innate ability of fish to detect predator olfactory cues. Ecology Letters, 13(1), 68-75, DOI: https://doi.org/10.1111/j.1461-0248.2009.01400.x
» https://doi.org/10.1111/j.1461-0248.2009.01400.x
Doherty, P. J. 1987. Light-traps: selective but useful devices for quantifying the distributions and abundances of larval fishes. Bulletin of Marine Science , 41(2), 423-431.
Erdman, D. S. 1977. Spawning patterns of fish from the northeastern Caribbean Rome: FAO Fisheries Reports (FAO).
Faraco, L. F. D., ANDRIGUETTO-FILHO, J. M., DAW, T., LANA, P. D. C. & TEIXEIRA, C. F. 2016. Vulnerability among fishers in southern Brazil and its relation to marine protected areas in a scenario of declining fisheries. Desenvolvimento e Meio Ambiente, 38(1), 51-76, DOI: https://doi.org/10.5380/dma.v38i0.45850
» https://doi.org/10.5380/dma.v38i0.45850
Fisher, R. 2005. Swimming speeds of larval coral reef fishes: impacts on self-recruitment and dispersal. Marine Ecology Progress Series, 285, 223-232, DOI: https://doi.org/10.3354/meps285223
» https://doi.org/10.3354/meps285223
Floeter, S. & Gasparini, J. L. 2000. The southeastern Atlantic reef fish fauna: composition and zoogeographic patterns. Journal of Fish Biology , 56(5), 1099-1114, DOI: https://doi.org/10.1111/j.1095-8649.2000.tb02126.x
» https://doi.org/10.1111/j.1095-8649.2000.tb02126.x
Froese, R. & Pauly, D. 2016. FishBase [online]. Available at: http://www.fishbase.org/Search.php [Accessed 13 Sep. 2016].
» http://www.fishbase.org/Search.php
Fujita, T., Kitagawa, D., Okuyama, Y., Jin, Y., Ishito, Y. & Inada, T. 1996. Comparison of fish assemblages among an artificial reef, a natural reef and a sandy-mud bottom site on the shelf off Iwate, northern Japan. Environmental Biology of Fishes, 46(4), 351-364, DOI: https://doi.org/10.1007/BF00005013
» https://doi.org/10.1007/BF00005013
Gaston, K. J. 1994. What is rarity?. In: GASTON, K. J. (ed). Rarity Dordrecht: Springer .
Gerhardinger, L. C., Freitas, M. O., Andrade, Á. B. & Rangel, C. A. 2006. Omobranchus punctatus (Teleostei: Blenniidae), an exotic blenny in the Southwestern Atlantic. Biological Invasions, 8, 941-946, DOI: https://doi.org/10.1007/s10530-005-5104-2
» https://doi.org/10.1007/s10530-005-5104-2
Golani, D. & Diamant, A. 1999. Fish colonization of an artificial reef in the Gulf of Elat, northern Red Sea.Environmental Biology of Fishes , 54(3), 275-282, DOI: https://doi.org/10.1023/A:1007528210270
» https://doi.org/10.1023/A:1007528210270
Gordon, T. A., Harding, H. R., Wong, K. E., Merchant, N. D., Meekan, M. G., McCormick, M. I., Radford, A. N. & Simpson, S. D. 2018. Habitat degradation negatively affects auditory settlement behavior of coral reef fishes. Proceedings of the National Academy of Sciences, 115(20), 5193-5198, DOI: https://doi.org/10.1073/pnas.1719291115
» https://doi.org/10.1073/pnas.1719291115
Grande, H., Rezende, S. D. M., Simon, T. E., Félix-Hackradt, F. C., García-Charton, J. A., Maida, M., Gaspar, A. L. B., Francini-Filho, R. B., Fredou, T. & Ferreira, B. P. 2019. Diversity of settlement-stage reef fishes captured by light-trap in a tropical south-west Atlantic Ocean coastal reef system. Journal of Fish Biology , 94(2), 210-222, DOI: https://doi.org/10.1111/jfb.13858
» https://doi.org/10.1111/jfb.13858
Grorud-Colvert, K. & Sponaugle, S. 2009. Larval supply and juvenile recruitment of coral reef fishes to marine reserves and non-reserves of the upper Florida Keys, USA. Marine Biology , 156(3), 277-288, DOI: https://doi.org/10.1007/s00227-008-1082-0
» https://doi.org/10.1007/s00227-008-1082-0
Hackradt, C. W. & Félix-Hackradt, F. C. 2009. Assembléia de peixes associados a ambientes consolidados no litoral do Paraná, Brasil: uma análise qualitativa com notas sobre sua bioecologia. Papéis Avulsos de Zoologia, 49(31), 389-403, DOI: http://dx.doi.org/10.1590/S0031-10492009003100001
» http://dx.doi.org/10.1590/S0031-10492009003100001
Hackradt, C. W., Félix-Hackradt, F. C. & García-Charton, J. A. 2011. Influence of habitat structure on fish assemblage of an artificial reef in southern Brazil. Marine Environmental Research, 72(5), 235-47, DOI: https://doi.org/10.1016/j.marenvres.2011.09.006
» https://doi.org/10.1016/j.marenvres.2011.09.006
Hellriegel, B. 2000. Single- or multistage regulation in complex life cycles: does it make a difference? Oikos, 88(2), 239-249, DOI: https://doi.org/10.1034/j.1600-0706.2000.880202.x
» https://doi.org/10.1034/j.1600-0706.2000.880202.x
Houde, E. D. 2008. Emerging from Hjort’s Shadow. Journal of Northwest Atlantic Fishery Science, 41, 53-70, DOI: https://doi:10.2960/J.v41.m634
» https://doi:10.2960/J.v41.m634
Jones, G. P., Planes, S. & Thorrold, S. R. 2005. Coral reef fish larvae settle close to home. Current Biology, 15(14), 1314-1318, DOI: https://doi.org/10.1016/j.cub.2005.06.061
» https://doi.org/10.1016/j.cub.2005.06.061
Jud, Z. R., Layman, C. A., Lee, J. A. & Arrington, D. A. 2011. Recent invasion of a Florida (USA) estuarine system by lionfish Pterois volitans/P. miles. Aquatic Biology, 13(1), 21-26, DOI: https://doi.org/10.3354/ab00351
» https://doi.org/10.3354/ab00351
Katsumiti, A., Domingos, F. V., Azevedo, M., Silva, M. D., Damian, R. C., Almeida, M. I. M., Silva de Assis, H. C., Cestari, M. M., Randi, M. A. F., Oliveria Ribeiro, C. A. & Freire, C. A. 2009. An assessment of acute biomarker responses in the demersal catfish Cathorops spixii after the Vicuña Oil Spill in a harbour estuarine area in Southern Brazil. Environmental Monitoring and Assessment, 152(1-4), 209, DOI: https://doi.org/10.1007/s10661-008-0309-3
» https://doi.org/10.1007/s10661-008-0309-3
Kendall, A., Ahlstrom, E. H. & Moser, H. G. 1984 Early life history stages of fishes and their characters. In: MOSER, H. G., RICHARDS, W. J., COHEN, D. M., FAHAY, M. P., KENDALL, A. W. & RICHARDSON, S. L. (eds.). Ontogeny and Systematics of Fishes Lawrence: American Society of Ichthyologists and Herpetologists.
Kingsford, M. J., Leis, J. M., Shanks, A., Lindeman, K., Morgan, S. & Pineda, J. 2002. Sensory environments, larval abilities and local self-recruitment. Bulletin of Marine Science , 70(1), 309-340.
Kolkovski, S., Arieli, A. & Tandler, A. 1997. Visual and chemical cues stimulate microdiet ingestion of sea bream larvae. Aquaculture Internatonal, 5, 527-536, DOI: https://doi.org/10.1023/A:1018305416501
» https://doi.org/10.1023/A:1018305416501
Lecchini, D., Mills, S. C., Brié, C., Lo, C. M. & Banaigs, B. 2011. Chemical stimuli in coral reefs: how butterflyfishes find their food.Environmental Biology of Fishes , 91(3), 303-309, DOI: https://doi.org/10.1007/s10641-011-9785-3
» https://doi.org/10.1007/s10641-011-9785-3
Leis, J. M. 1989. Larval biology of butterflyfishes (Pisces, Chaetodontidae): what do we really know?. In: MOTTA, P. J. (ed.). The butterflyfishes: success on the coral reef Dordrecht: Springer . pp. 87-100.
Leis, J. M. 1991. Vertical distribution of fish larvae in the Great Barrier Reef Lagoon, Australia. Marine Biology , 109(1), 157-166, DOI: https://doi.org/10.1007/BF01320243
» https://doi.org/10.1007/BF01320243
Leis, J. M. & Carson-Ewart, B. M. 2000. The larvae of Indo-Pacific coastal fishes: an identification guide to marine fish larvae Boston: Brill.
Leis, J. M., Carson-Ewart, B. M. & Cato, D. H. 2002. Sound detection in situ by the larvae of a coral-reef damselfish (Pomacentridae). Marine Ecology Progress Series, 232, 259-268, DOI: https://doi.org/10.3354/meps232259
» https://doi.org/10.3354/meps232259
Leis, J. M., Chuenpagdee, R. & Medeiros, R. P. 2019. Where small-scale fisheries meet conservation boundaries: MPA Governance Challenges in Southern Brazil. In: Salas, S., Barragán-Paladines, M. & Chuenpagdee, R. (eds.). Viability and sustainability of small-scale fisheries in Latin America and the Caribbean Cham: Springer. pp. 453-472, DOI: https://doi.org/10.1007/978-3-319-76078-0_19
» https://doi.org/10.1007/978-3-319-76078-0_19
Leis, J. M. & Goldman, B. 1987. Composition and distribution of larval fish assemblages in the Great Barrier Reef Lagoon, near Lizard Island, Australia. Marine and Freshwater Research , 38(2), 211-223, DOI: https://doi.org/10.1071/MF9870211
» https://doi.org/10.1071/MF9870211
Leis, J. M., Siebeck, U. & Dixson, D. L. 2011. How Nemo finds home: the neuroecology of dispersal and of population connectivity in larvae of marine fishes. Integrative and Comparative Biology, 51(5), 826-843, DOI: https://doi.org/10.1093/icb/icr004
» https://doi.org/10.1093/icb/icr004
Lindberg, W. J. 1997. Can science resolve the attraction-production issue?. Fisheries, 22(4), 10-13, DOI: https://doi.org/10.1577/1548-8446-22-4
» https://doi.org/10.1577/1548-8446-22-4
Macedo-Soares, L. C., Birolo, A. B. & Freire, A. S. 2009. Spatial and temporal distribution of fish eggs and larvae in a subtropical coastal lagoon, Santa Catarina State, Brazil. Neotropical Ichthyology, 7(2), 231-240, DOI: http://dx.doi.org/10.1590/S1679-62252009000200015
» http://dx.doi.org/10.1590/S1679-62252009000200015
Martin, T. G., Wintle, B. A., Rhodes, J. R., Kuhnert, P. M., Field, S. A., Low-Choy, S. J., Tyre, A. J. & Possingham, H. P. 2005. Zero tolerance ecology: improving ecological inference by modelling the source of zero observations. Ecology Letters, 8(11), 1235-1246, DOI: https://doi.org/10.1111/j.1461-0248.2005.00826.x
» https://doi.org/10.1111/j.1461-0248.2005.00826.x
Matsuura, Y. 1977. A study of the life history of Brazilian sardine, Sardinella brasiliensis: IV. Distribution and abundance of sardine larvae. Boletim do Instituto Oceanográfico, 26(2), 219-247, DOI: http://dx.doi.org/10.1590/S0373-55241977000200002
» http://dx.doi.org/10.1590/S0373-55241977000200002
McNeill, G., Nunn, J. & Minchin, D. 2010. The slipper limpet Crepidula fornicata Linnaeus, 1758 becomes established in Ireland. Aquatic Invasions , 5, S21-S25, DOI: http://dx.doi.org/10.3391/ai.2010.5.S1.006
» http://dx.doi.org/10.3391/ai.2010.5.S1.006
Montgomery, J. C., Jeffs, A., Simpson, S. D., Meekan, M. & Tindle, C. 2006. Sound as an orientation cue for the pelagic larvae of reef fishes and decapod crustaceans. Advances in Marine Biology , 5, 143-96, DOI: https://doi.org/10.1016/S0065-2881(06)51003-X
» https://doi.org/10.1016/S0065-2881(06)51003-X
Murphy, B. R. & Willis, D. W. 1996. Fisheries techniques 2nd ed. Bethesda: American Fisheries Society.
Nelson, J. S., Grande, T. C. & Wilson, M. V. 2016. Fishes of the world New York: John Wiley & Sons.
NOERNBERG, M. A., MIZERKOWSKI, B. D., PALOSCHI, N. G. & BENTO, J. P. 2014. Hydrodynamics and bio-optical assessment of two pristine subtropical estuaries in southern Brazil.Brazilian Journal of Oceanography , 62(4), 265-278, DOI: https://doi.org/10.1590/s1679-87592014069006204
» https://doi.org/10.1590/s1679-87592014069006204
NOGUEIRA JUNIOR, M. & BRANDINI, F. P. 2018. Community structure and spatiotemporal dynamics of the zooplankton in the South Brazilian Bight: a review. In:NOGUEIRA JUNIOR, M. & BRANDINI, F. P. (eds.). Plankton Ecology of the Southwestern Atlantic Cam: Springer. pp. 149-170, DOI: https://doi.org/10.1007/978-3-319-77869-3_8
» https://doi.org/10.1007/978-3-319-77869-3_8
Nonaka, R. H., Matsuura, Y. & Suzuki, K. 2000. Seasonal variation in larval fish assemblages in relation to oceanographic conditions in the Abrolhos Bank region off eastern Brazil. Fishery Bulletin , 98(4), 767-784.
Osenberg, C. W., Mary, S. t. C. M., Wilson, J. A. & Lindberg, W. J. 2002. A quantitative framework to evaluate the attraction-production controversy. ICES Journal of Marine Science, 59(Suppl 1), S214-S221, DOI: https://doi.org/10.1006/jmsc.2002.1222
» https://doi.org/10.1006/jmsc.2002.1222
Pinheiros, P. C. 2005. Ictiofauna do arquipélago de Currais (Paraná-Brasil): complexidade estrutural dos costões rochosos e análises comparativa com um módulo recifal artificial DSc. São Carlos: Universidade Federal de São Carlos.
Richards, W. J. 2006. Early stages of atlantic fishes: an identification guide for the Western Central North Atlantic Abingdon: Taylor & Francis.
Santos, L. O. 2014. Relatório Técnico-Científico: Licença de Instalação no 887/2012 referente ao lançamento de estruturas de recifes artificiais ao longo do litoral do Estado do Paraná (Processo nº 02017.005865/2005-21). Paraná: Diretoria de Pesquisas Coordenação de Contas Nacionais.
Santos, L. N., Brotto, D. S. & Zalmon, I. R. 2010. Fish responses to increasing distance from artificial reefs on the Southeastern Brazilian Coast. Journal of Experimental Marine Biology and Ecology , 386(1-2), 54-60, DOI: https://doi.org/10.1016/j.jembe.2010.01.018
» https://doi.org/10.1016/j.jembe.2010.01.018
Stephens JUNIOr, J. & Pondella, D. 2002. Larval productivity of a mature artificial reef: the ichthyoplankton of King Harbor, California, 1974-1997. ICES Journal of Marine Science , 59(Suppl 1), S51-S58, DOI: https://doi.org/10.1006/jmsc.2002.1189
» https://doi.org/10.1006/jmsc.2002.1189
Svane, I. B. & Petersen, J. K. 2001. On the problems of epibioses, fouling and artificial reefs, a review. Marine Ecology , 22(3), 169-188, DOI: https://doi.org/10.1046/j.1439-0485.2001.01729.x
» https://doi.org/10.1046/j.1439-0485.2001.01729.x
Thorrold, S. R. 1992. Evaluating the performance of light traps for sampling small fish and squid in open waters of the central Great Barrier Reef lagoon. Marine Ecology Progress Series, 89(2), 277-285.
Tyre, A. J., Tenhumberg, B., Field, S. A., Niejalke, D., Parris, K. & Possingham, H. P. 2003. Improving precision and reducing bias in biological surveys: estimating false-negative error rates. Ecological Applications, 13(6), 1790-1801, DOI: https://doi.org/10.1890/02-5078
» https://doi.org/10.1890/02-5078
Vaselli, S., Bulleri, F. & Benedetti-Cecchi, L. 2008. Hard coastal-defense structures as habitats for native and exotic rocky-bottom species. Marine Environmental Research , 66(4), 395-403, DOI: https://doi.org/10.1016/j.marenvres.2008.06.002
» https://doi.org/10.1016/j.marenvres.2008.06.002
Victor, B. C. 1991. Settlement strategies and biogeography of reef fishes. In: SALE, P. F. (ed.). The ecology of fishes on coral reefs San Diego: Academic Press .
Walsh, W. J. 1985. Reef fish community dynamics on small artificial reefs: the influence of isolation, habitat structure, and biogeography. Bulletin of Marine Science , 36(2), 357-376.
Whitehead, P. J. P. 1988. FAO species catalogue: an annotated and illustrated catalogue of the herrings, sardines, pilchards, sprats, shads, anchovies and wolf-herrings Rome: FAO Fisheries Synopsis.
Wiebe, P. H. 1971. A computer model study of zooplankton patchiness and its effects on sampling error 1. Limnology and Oceanography, 16(1), 29-38, DOI: https://doi.org/10.4319/lo.1971.16.1.0029
» https://doi.org/10.4319/lo.1971.16.1.0029
Wiebe, P. H. & Wiebe, P. H. 1968. Plankton patchiness: effects on repeated net tows 1. Limnology and Oceanography , 13(2), 315-321, DOI: https://doi.org/10.4319/lo.1968.13.2.0315
» https://doi.org/10.4319/lo.1968.13.2.0315
Wilhelmsson, D., Malm, T. & Öhman, M. C. 2006. The influence of offshore wind power on demersal fish. ICES Journal of Marine Science , 63(5), 775-784, DOI: https://doi.org/10.1016/j.icesjms.2006.02.001
