Movement, connectivity and population structure of the intertidal fish Lipophrys pholis as revealed by otolith oxygen and carbon stable isotopes

References

• Almada VC, Barata EN, Gonçalves EJ, Oliveira RF. 1990. On the breeding season of Lipophrys pholis (Pisces: Blenniidae) at Arrábida, Portugal. Journal of the Marine Biological Association of the United Kingdom 70:913–16. doi: 10.1017/S0025315400059142
   Google Scholar
• Almada VC, Oliveira RF, Gonçalves EJ, Almeida AJ, Santos RS, Wirtz P. 2001. Patterns of diversity of the north-eastern Atlantic blenniid fish fauna (Pisces: Blenniidae). Global Ecology and Biogeography 10:411–22. doi: 10.1046/j.1466-822X.2001.00244.x
   Google Scholar
• Azeiteiro UL, Bacelar-Nicolau L, Resende R, Gonçalves F, Pereira MJ. 2006. Larval fish distribution in shallow coastal waters off North Western Iberia (NE Atlantic). Estuarine, Coastal and Shelf Science 69:554–66. doi: 10.1016/j.ecss.2006.05.023
   Google Scholar
• Campana SE. 1999. Chemistry and composition of fish otoliths: pathways, mechanisms and applications. Marine Ecology Progress Series 188:263–97. doi: 10.3354/meps188263
   Google Scholar
• Carvalho MG, Moreira C, Queiroga H, Santos PT, Correia, AT. 2017a. Age, growth and sex of the shanny, Lipophrys pholis (Linnaeus, 1758) (Teleostei, Blenniidae), from the NW coast of Portugal. Journal of Applied Ichthyology 33:242–51. doi:10.1111/jai.13307 doi: 10.1111/jai.13307
   Google Scholar
• Carvalho MG, Moreira C, Queiroga H, Santos PT, Correia, AT. 2017b. Pelagic larval duration, size at settlement and coastal recruitment of the intertidal blenny Lipophrys pholis. Journal of the Marine Biological Association of the United Kingdom 97:197–205. doi: 10.1017/S0025315415002179
   Google Scholar
• Correia AT, Barros F, Sial AN. 2011. Stock discrimination of European conger eel (Conger conger L.) using otolith stable isotope ratios. Fisheries Research 108:88–94. doi: 10.1016/j.fishres.2010.12.002
   Google Scholar
• Daros FA, Spach HL, Sial AN, Correia AT. 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 3:262–72. doi: 10.1016/j.rsma.2015.11.012
   Google Scholar
• Elsdon TS, Gillanders BM. 2002. Interactive effects of temperature and salinity on otolith chemistry: challenges for determining environmental histories of fish. Canadian Journal of Fisheries and Aquatic Sciences 59:1796–808. doi: 10.1139/f02-154
   Google Scholar
• Faria C, Almada VC. 2001a. Microhabitat segregation in three rocky intertidal fish species in Portugal: does it reflect interspecific competition? Journal of Fish Biology 58:145–59. doi: 10.1111/j.1095-8649.2001.tb00504.x
   Google Scholar
• Faria C, Almada VC. 2001b. 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. doi: 10.1007/s102110100042
   Google Scholar
• Faria C, Almada VC, Gonçalves EJ. 1996. Juvenile recruitment, growth and maturation of Lipophrys pholis (Pisces: Blenniidae), from the west coast of Portugal. Journal of Fish Biology 49:727–30.
   Google Scholar
• Faria C, Borges R, Gil F, Almada VC, Gonçalves E. 2002. Embryonic and larval development of Lipophrys pholis (Pisces: Blenniidae). Scientia Marina 66:21–26. doi: 10.3989/scimar.2002.66n121
   Google Scholar
• Fisher R. 2005. Swimming speeds of larval coral reef fishes: impacts on self-recruitment and dispersal. Marine Ecology Progress Series 285:223–32. doi: 10.3354/meps285223
   Google Scholar
• Francisco SM, Vieira MN, Almada VC. 2006. Genetic structure and historical demography of the shanny Lipophrys pholis in the Portuguese coast based on mitochondrial DNA analysis. Molecular Phylogenetics and Evolution 39:288–92. doi: 10.1016/j.ympev.2005.12.009
   Google Scholar
• Gao Y, Joner SH, Svec RA, Weinberg KL. 2004. Stable isotopic comparison in otoliths of juvenile sablefish (Anoplopoma fimbria) from waters off the Washington and Oregon coast. Fisheries Research 68:351–60. doi: 10.1016/j.fishres.2003.11.002
   Google Scholar
• Geffen A. 2012. Otolith oxygen and carbon stable isotopes in wild and laboratory-reared plaice (Pleuronectes platessa). Environmental Biology of Fishes 95:419–30. doi: 10.1007/s10641-012-0033-2
   Google Scholar
• Gerard T, Muhling B. 2010. Variation in the isotopic signatures of juvenile gray snapper (Lutjanus griseus) from five southern Florida regions. Fishery Bulletin 108:98–105.
   Google Scholar
• Gibson RN. 1982. Recent studies on the biology of intertidal fishes. Oceanography and Marine Biology: An Annual Review 20:363–414.
   Google Scholar
• Hickford MJH, Schiel DR. 2003. Comparative dispersal of larvae from demersal versus pelagic spawning fishes. Marine Ecology Progress Series 252:255–71. doi: 10.3354/meps252255
   Google Scholar
• Høie H, Folkvord A, Otterlei E. 2003. Effect of somatic and otolith growth rate on stable isotopic composition of early juvenile cod (Gadus morhua L.) otoliths. Journal of Experimental Marine Biology and Ecology 289:41–58. doi: 10.1016/S0022-0981(03)00034-0
   Google Scholar
• Høie H, Otterlei E, Folkvord A. 2004. Temperature-dependent fractionation of stable oxygen isotopes in otoliths of juvenile cod (Gadus morhua L.). ICES Journal of Marine Science 61:243–51. doi: 10.1016/j.icesjms.2003.11.006
   Google Scholar
• Leis JM, Hay AC, Trnski T. 2006. In situ ontogeny of behaviour in pelagic larvae of three temperate, marine, demersal fishes. Marine Biology 148:655–69. doi: 10.1007/s00227-005-0108-0
   Google Scholar
• Lima FP, Queiroz N, Ribeiro PA, Hawkins SJ, Santos AM. 2006. Recent changes in the distribution of a marine gastropod, Patella rustica Linnaeus, 1758, and their relationship to unusual climatic events. Journal of Biogeography 33:812–22. doi: 10.1111/j.1365-2699.2006.01457.x
   Google Scholar
• Matta ME, Orland IJ, Ushikubo T, Helser TE, Black BA, Valley JW. 2013. Otolith oxygen isotopes measured by high-precision secondary ion mass spectrometry reflect life history of a yellowfin sole (Limanda aspera). Rapid Communications in Mass Spectrometry 27:691–99. doi: 10.1002/rcm.6502
   Google Scholar
• Otero P, Ruiz-Villarreal M, Peliz A. 2008. Variability of river plumes off Northwest Iberia in response to wind events. Journal of Marine Systems 72:238–55. doi: 10.1016/j.jmarsys.2007.05.016
   Google Scholar
• Radtke RL, Showers W, Moksness E, Lenz P. 1996. Environmental information stored in otoliths: insights from stable isotopes. Marine Biology 127:161–70. doi:10.1007/BF00993656
   Google Scholar
• Qasim SZ. 1957. The biology of Blennius pholis L. (Teleostei). Proceedings of the Zoological Society of London 128:161–208. doi: 10.1111/j.1096-3642.1957.tb00264.x
   Google Scholar
• Schwarcz HP, Gao Y, Campana S, Browne D, Knyf M, Brand U. 1998. Stable carbon isotope variations in otoliths of Atlantic cod (Gadus morhua). Canadian Journal of Fisheries and Aquatic Sciences 55:1798–806. doi: 10.1139/f98-053
   Google Scholar
• Shiao JC, Wang SW, Yokawa K, Ichinokawa M, Takeuchi Y, Chen YG, Shen CC. 2010. Natal origin of Pacific bluefin tuna Thunnus orientalis inferred from otolith oxygen isotope composition. Marine Ecology Progress Series 420:207–19. doi: 10.3354/meps08867
   Google Scholar
• Solomon CT, Weber PK, Cech Jr JJ, Ingram BL, Conrad ME, Machavaram MV, et al. 2006. Experimental determination of the sources of otolith carbon and associated isotopic fractionation. Canadian Journal of Fisheries and Aquatic Sciences 63:79–89. doi: 10.1139/f05-200
   Google Scholar
• Thorrold SR, Campana SE, Jones CM, Swart PK. 1997. Factors determining δ13C and δ18O fractionation in aragonitic otoliths of marine fish. Geochimica et Cosmochimica Acta 61:2909–19. doi: 10.1016/S0016-7037(97)00141-5
   Google Scholar
• Valle SR, Herzka SZ. 2008. Natural variability in δ18O values of otoliths of young Pacific sardine captured in Mexican waters indicates subpopulation mixing within the first year of life. ICES Journal of Marine Science 65:174–90. doi: 10.1093/icesjms/fsn001
   Google Scholar
• Vieira MEC, Bordalo AA. 2000. The Douro estuary (Portugal): a mesotidal salt wedge. Oceanologica Acta 23:585–94. doi: 10.1016/S0399-1784(00)01107-5
   Google Scholar
• Yoshimura T, Izumida H, Nakashima R, Ishimura T, Shikazono N, Kawahata H, Suzuki A. 2015. Stable carbon isotope values in dissolved inorganic carbon of ambient waters and shell carbonate of the freshwater pearl mussel (Hyriopsis sp.). Journal of Paleolimnology 54:37–51. doi: 10.1007/s10933-015-9834-6
   Google Scholar
• Zander CD. 1986. Blenniidae. In: Whitehead P, Bauchot ML, Hureau JC, Nielsen J, Tortonese E, editors. Fishes of the North-eastern Atlantic and the Mediterranean. Paris: UNESCO, p 1096–112.
   Google Scholar