Early-life history traits of Thalassoma bifasciatum in Culebra, Puerto Rico
DOI:
https://doi.org/10.15517/a6w5bd45Keywords:
coral reef; otolith; aging; condition factor.Abstract
Introduction: The study of labrid otoliths has contributed significantly to our understanding of life histories of tropical reef fish. Life history theory is based on the effect on lifetime reproductive success (i.e., fitness), growth, mortality rates, age at maturity, reproductive output, and particularly for reef fish age and size at settlement of pelagic larvae to benthic juveniles.
Objective: Quantify age and larval growth at settlement, subsequent length, and body condition of Thalassoma bifasciatum.
Methods: Two hundred T. bifasciatum individuals were collected from Punta Maguey, in Culebra, Puerto Rico. One hundred individuals were euthanized for otolith dissection.
Results: Otolith analyses revealed settlement ages ranging from 10 to 37 days and estimated standard length of 9–20 mm at settlement. Growth analyses demonstrated a significant positive relationship between age and length, while length – weight regression revealed a negative allometric growth, where length increases at a faster rate than body mass (b < 3). Additionally, Fulton’s condition factor declined with the increasing length.
Conclusions: This study highlights early life history and growth patterns in T. bifasciatum in Culebra, PR and underscores the need for further exploration of life history traits to better understand population dynamics of tropical reef fishes. The rapid settlement observed in our study may be attributed to elevated water temperatures, suggesting that environmental drivers play a critical role in shaping recruitment and growth. This emphasizes the importance of incorporating environmental drivers when evaluating recruitment and population structure.
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References
Ackerman, J. (2004). Geographic variation in size at age of the coral reef fish, Thalassoma lunare (Family: Labridae): a contribution to life history theory [Doctoral dissertation]. James Cook University, Australia. https://researchonline.jcu.edu.au/66/
Booth, D. J., & Beretta, G. A. (2004). Influence of recruit condition on food competition and predation risk in a coral reef fish. Oecologia, 140, 289–294. https://doi.org/10.1007/s00442-004-1608-1
Campana, S. E., & Thorrold, S. R. (2001). Otoliths, increments, and elements: keys to a comprehensive understanding of fish populations? Canadian Journal Of Fisheries And Aquatic Sciences, 58(1), 30–38. https://doi.org/10.1139/f00-177
Chittaro, P., Veggerby, K., Haught, K., & Sanderson, B. (2020). Otolith processing and analysis [Technical report]. National Oceanic and Atmospheric Administration, United States of America. https://doi.org/10.25923/Nwy5-Qe26
Choat, J. H., Robertson, D. R., Ackerman, J. L., & Posada, J. M. (2003). An age-based demographic analysis of the Caribbean stoplight parrotfish Sparisoma viride. Marine Ecology Progress Series, 246, 265–277. https://doi.org/10.3354/meps246265
Depczynski, M., & Bellwood, D. R. (2006). Extremes, plasticity, and invariance in vertebrate life history traits: insights from coral reef fishes. Ecology, 87(12), 3119–3127. https://doi.org/10.1890/0012-9658(2006)87[3119:EPAIIV]2.0.CO;2
Green, B. S., & Fisher, R. (2004). Temperature influences swimming speed, growth and larval duration in coral reef fish larvae. Journal of Experimental Marine Biology and Ecology, 299(1), 115–132. https://doi.org/10.1016/j.jembe.2003.09.001
Grorud-Colvert, K., & Sponaugle, S. (2006). Influence of condition on behavior and survival potential of a newly settled coral reef fish, the Bluehead Wrasse Thalassoma bifasciatum. Marine Ecology Progress Series, 327, 279–288. https://doi.org/10.3354/meps327279
Hamilton, S., & Warner, R. (2009). Otolith barium profiles verify the timing of settlement in a coral reef fish. Marine Ecology Progress Series, 385, 237–244. https://doi.org/10.3354/meps08054
Hensley, D. A., Appeldoorn, R. S., Shapiro, D. Y., Ray, M., & Turingan, R. G. (1994). Egg Dispersal in a Caribbean Coral Reef Fish, Thalassoma Bifasciatum. I. Dispersal Over the Reef Platform. Bulletin of Marine Science, 54(1), 256–270.
Hernández-Delgado, E. A., Fonseca-Miranda, J. S., Mercado-Molina, A. E., & Suleimán-Ramos, S. E. (2025). Integrating 3D-printed and natural staghorn coral (Acropora cervicornis) restoration enhances fish assemblages and their ecological functions. Diversity, 17, 445. https://doi.org/10.3390/d17070445
Hernández-Delgado, E. A., & Rodríguez-González, Y. M. (2025). Runaway climate across the wider Caribbean and Eastern Tropical Pacific in the Anthropocene: threats to coral reef conservation, restoration, and social–ecological resilience. Atmosphere, 16(5), 575. https://doi.org/10.3390/atmos16050575
Hoffman, S. G., Schildhauer, M. P., & Warner, R. R. (1985). The costs of changing sex and the ontogeny of males under contest competition for mates. Evolution, 39(4), 915–927. https://doi.org/10.1111/J.1558-5646.1985.Tb00432.X
Houde, E. D., & Zastrow, C. E. (1993). Ecosystem-and taxon-specific dynamic and energetics properties of larval fish assemblages. Bulletin Of Marine Science, 53(2), 290–335.
Huang, M., Ding, L., Wang, J., Ding, C., & Tao, J. (2021). The impacts of climate change on fish growth: a summary of conducted studies and current knowledge. Ecological Indicators, 121, 106976. https://doi.org/10.1016/j.ecolind.2020.106976
Jones, C. M. (1992). Chapter 1: Development and application of the otolith increment technique. In D. K. Stevenson & S. E. Campana (Eds.), Canadian Special Publication Of Fisheries And Aquatic Sciences (Vol. 117, pp. 1–11). Department of Fisheries and Oceans, Canada.
Masterson, C. F., Danilowicz, B. S., & Sale, P. F. (1997). Yearly and inter-island variation in the recruitment dynamics of the bluehead wrasse (Thalassoma bifasciatum, Bloch). Journal Of Experimental Marine Biology And Ecology, 214(1–2), 149–166. https://doi.org/10.1016/S0022-0981(97)00020-8
Mazumder, S. K., De, M., Mazlan, A. G., Zaidi, C. C., Rahim, S. M., & Simon, K. D. (2015). Impact of global climate change on fish growth, digestion and physiological status: developing a hypothesis for cause and effect relationships. Journal Of Water And Climate Change, 6(2), 200–226. https://doi.org/10.2166/Wcc.2014.146
McCormick, M. I., & 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. https://doi.org/10.3354/meps118059
Ménard, A., Turgeon, K., Roche, D. G., Binning, S. A., & Kramer, D. L. (2012). Shelters and their use by fishes on fringing coral reefs. PLoS One, 7(6), e38450. https://doi.org/10.1371/journal.pone.0038450
Pawson, M. G. (1990). Using otolith weight to age fish. Journal of Fish Biology, 36(4), 521–531. https://doi.org/10.1111/j.1095-8649.1990.tb03554.x
Philibotte, J. (2002). Pelagic larval duration of the caribbean wrasse, Thalassoma bifasciatum. Biological Bulletin, 203(2), 245–246.
Prescod, A. C. (2015). Thalassoma bifasciatum (Bluehead Wrasse): The Online Guide to the Animals of Trinidad and Tobago. The University of the West Indies. https://sta.uwi.edu/fst/lifesciences/sites/default/files/lifesciences/documents/ogatt/Thalassoma_bifasciatum%20-%20Bluehead%20Wrasse.pdf
Rodríguez Mendoza, R. P. R. (2006). Otoliths and their applications in fishery science. Croatian Journal Of Fisheries, 64(3), 89–102.
Robertson, D. R. (1992). Patterns of lunar settlement and early recruitment in Caribbean reef fishes at Panamá. Marine Biology, 114(4), 527–537. https://doi.org/10.1007/Bf00357250
R Studio Team. (2024). RStudio: Integrated development environment for R (Version 2023.12.1+402 “Ocean Storm”) [Computer software]. Posit Software, PBC. https://posit.co/
Schneider, C., Rasband, W., & Eliceiri, K. (2012). NIH Image to ImageJ: 25 years of image analysis. Nature Methods, 9, 671–675. https://doi.org/10.1038/nmeth.2089
Schultz, E. T., & Warner, R. R. (1989). Phenotypic plasticity in life-history traits of female Thalassoma bifasciatum (Pisces: Labridae). 1. Manipulations of social structure in tests for adaptive shifts of life-history allocations. Evolution, 43(7). 1497–1506. https://doi.org/10.1111/j.1558-5646.1989.tb02599.x
Schultz, E. T., & Warner, R. R. (1991). Phenotypic plasticity in life-history traits of female Thalassoma bifasciatum (Pisces: Labridae): 2. Correlation of fecundity and growth rate in comparative studies. Environmental Biology of Fishes, 30, 333–344. https://doi.org/10.1007/BF02028849
Searcy, S. P., & Sponaugle, S. (2000). Variable larval growth in a coral reef fish. Marine Ecology Progress Series, 206, 213–226. https://doi.org/10.3354/meps206213
Shea, S., Liu, M. &, & Sadovy, Y. (2010). Thalassoma bifasciatum. The IUCN Red List Of Threatened Species. https://doi.org/10.2305/Iucn.Uk.2010
Sponaugle, S., & Cowen, R. K. (1997). Early life history traits and recruitment patterns of caribbean wrasses (Labridae). Ecological Monographs, 67(2), 177–202. https://doi.org/10.1890/0012-9615(1997)067[0177:ELHTAR]2.0.CO;2
Sponaugle, S., & Grorud-Colvert, K. (2006). Environmental variability, early life-history traits, and survival of new coral reef fish recruits. Integrative And Comparative Biology, 46(5), 623–633. https://doi.org/10.1093/icb/icl014
Sponaugle, S., Llopiz, J., Havel, L., & Rankin, T. (2009). Spatial variation in larval growth and gut fullness in a coral reef fish. Marine Ecology Progress Series, 383, 239–249. https://doi.org/10.3354/meps07988
Sponaugle, S., & Pinkard, D. R. (2004). Impact of variable pelagic environments on natural larval growth and recruitment of the reef fish Thalassoma bifasciatum. Journal Of Fish Biology, 64(1), 34–54. https://doi.org/10.1111/J.1095-8649.2004.00279.X
Su, C., Shan, X., Jin, X., Han, Q., Chen, W., & Gorfine, H. (2024). Simulated reproductive allocation to fisheries-induced evolution among small yellow croaker populations in The Yellow and Bohai Seas. Ecological Indicators, 161, 111939. https://doi.org/10.1016/J.Ecolind.2024.111939
Sultan, S. E., & Spencer, H. G. (2002). Metapopulation structure favors plasticity over local adaptation. The American Naturalist, 160(2), 271–283. https://doi.org/10.1086/341015
Sun, Z. X., & Lobel, P. S. (2023). Pelagic larval duration of the meso-american reef fish, Halichoeres socialis (Labridae). Environmental Biology Of Fishes, 106, 1971–1982. https://doi.org/10.1007/S10641-023-01477-Z
Thunell, V., Gårdmark, A., Huss, M., & Vindenes, Y. (2023). Optimal energy allocation trade-off driven by size-dependent physiological and demographic responses to warming. Ecology, 104(4), e3967. https://doi.org/10.1002/ecy.3967
Victor, B. C. (1982). Daily otolith increments and recruitment in two coral-reef wrasses, Thalassoma bifasciatum and Halichoeres bivittatus. Marine Biology, 71, 203–208. https://doi.org/10.1007/BF00394631
Victor, B. C. (1986). Larval settlement and juvenile mortality in a recruitment-limited coral reef fish population. Ecological Monographs, 56(2), 145–160. https://doi.org/10.2307/1942506
Victor, B. C. (1991). Chapter 9: Settlement strategies and biogeography of reef fishes. In P. F. Sale (Ed.), The Ecology Of Fishes On Coral Reefs (pp. 231–260). Academic Press. https://doi.org/10.1016/B978-0-08-092551-6.50014-3
Walker, S. P. W. W., & McCormick, M. I. (2004). Otolith-check formation and accelerated growth associated with sex change in an annual protogynous tropical fish. Marine Ecology Progress Series, 266, 201–212. https://doi.org/10.3354/meps266201
Warner, R. R. (1984). Mating behavior and hermaphroditism in coral reef fishes: the diverse forms of sexuality found among tropical marine fishes can be viewed as adaptations to their equally diverse mating systems. Sigma Xi, The Scientific Research Society, 72(2), 128–136.
Warner, R. R. (1987). Female choice of sites versus mates in a coral reef fish, Thalassoma bifasciatum. Animal Behaviour, 35(5), 1470–1478. https://doi.org/10.1016/S0003-3472(87)80019-2
Warner, R. R. (1995). Large mating aggregations and daily long-distance spawning migrations in the bluehead wrasse, Thalassoma bifasciatum. Environmental Biology Of Fishes, 44, 337–345. https://doi.org/10.1007/Bf00008248
Warner, R. R. (1998). The role of extreme iteroparity and risk avoidance in the evolution of mating systems. Journal of Fish Biology, 53(sA), 82–93. https://doi.org/10.1111/j.1095-8649.1998.tb01019.x
Warner, R. R. (2000). Courtship displays and coloration as indicators of safety rather than quality in the bluehead wrasse. Behavioral Ecology, 11(4), 444–451. https://doi.org/10.1093/beheco/11.4.444
Warner, R. R., & Hoffman, S. G. (1980). Local population size as a determinant of mating system and sexual composition in two tropical marine fishes (Thalassoma spp.). Evolution, 34(3), 508–518. https://doi.org/10.2307/2408220
Warner, R. R., & Robertson, D. R. (1978). Sexual patterns in the labroid fishes of the western caribbean, I: the wrasses (Labridae) (Number 254). Smithsonian Contributions To Zoology.
Wilson, D. T., & Mccormick, M. I. (1997). Spatial and temporal validation of settlement-marks in the otoliths of tropical reef fishes. Marine Ecology Progress Series, 153, 259–271. https://doi.org/10.3354/meps153259
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