Abstract
Fish abundance is often better predicted by microhabitat variables on continuous reefs than on isolated patch reefs. Although this was suggested to stem from reduced post-recruitment relocation, this has not been shown experimentally. We found the relationship between the presence of a coral-dwelling fish, Dascyllus marginatus, and the size of its coral host to differ between corals on continuous reefs and the sparsely distributed corals on sandy bottoms. Empty transplanted corals were colonized exclusively by new recruits when on the sandy bottom, and both by new recruits and post-recruitment dispersal of adults when on the continuous reef. New recruits settled predominantly into small corals, although analyses of recruitment patterns were confounded by low recruitment in the studied years. Both tank experiments and field survey data suggest that the presence of recruits in small corals is at least partially driven by predation by the dottyback, Pseudochromis olivaceus, which lives predominantly in large corals within both habitats. Consequently, we suggest that the relationship between fish presence and coral size differs between the habitats due to coral size dependent predation on recruits and variability in the importance of direct recruitment to replenish fish populations.
Similar content being viewed by others
References
Almany GR (2004) Does increased habitat complexity reduce predation and competition in coral reef fish assemblages? Oikos 106:275–284. doi:https://doi.org/10.1111/j.0030-1299.2004.13193.x
Almany GR, Webster MS (2004) Odd species out as predators reduce diversity of coral-reef fishes. Ecology 85:2933–2937. doi:https://doi.org/10.1890/03-3150
Almany GR, Webster MS (2006) The predation gauntlet: early post-settlement mortality in reef fishes. Coral Reefs 25:19–22. doi:https://doi.org/10.1007/s00338-005-0044-y
Ault TR, Johnson CR (1998a) Spatially and temporally predictable fish communities on coral reefs. Ecol Monogr 68:25–50
Ault TR, Johnson CR (1998b) Relationships between habitat and recruitment of three species of damselfish (Pomacentridae) at Heron Reef, Great Barrier Reef. J Exp Mar Biol Ecol 223:145–166. doi:https://doi.org/10.1016/S0022-0981(97)00158-5
Beets J (1997) Effects of a predatory fish on the recruitment and abundance of Caribbean coral reef fishes. Mar Ecol Prog Ser 148:11–21. doi:https://doi.org/10.3354/meps148011
Belmaker J, Shashar N, Ziv Y (2005) Effects of small-scale isolation and predation on fish diversity on experimental reefs. Mar Ecol Prog Ser 289:273–283. doi:https://doi.org/10.3354/meps289273
Belmaker J, Ben-Moshe N, Ziv Y, Shashar N (2007a) Determinants of the steep species-area relationship of coral reef fishes. Coral Reefs 26:103–112. doi:https://doi.org/10.1007/s00338-006-0162-1
Belmaker J, Polak O, Shashar N, Ziv Y (2007b) Geographic divergence in the relationship between Paragobiodon echinocephalus and its obligate coral host. J Fish Biol 71:1555–1561. doi:https://doi.org/10.1111/j.1095-8649.2007.01619.x
Ben Tzvi O (2008) Dispersal and recruitment of coral reef fishes: a case study from the northern Gulf of Aqaba. PhD dissertation, Tel-Aviv University, Tel-Aviv, Israel
Beukers JS, Jones GP (1998) Habitat complexity modifies the impact of piscivores on a coral reef fish population. Oecologia 114:50–59. doi:https://doi.org/10.1007/s004420050419
Booth DJ (2002) Distribution changes after settlement in six species of damselfish (Pomacentridae) in one tree island lagoon, Great Barrier Reef. Mar Ecol Prog Ser 226:157–164. doi:https://doi.org/10.3354/meps226157
Carr MH, Hixon MA (1995) Predation effects on early postsettlement survivorship of coral-reef fishes. Mar Ecol Prog Ser 124:31–42. doi:https://doi.org/10.3354/meps124031
Doherty PJ, Dufour V, Galzin R, Hixon MA, Meekan MG, Planes S (2004) High mortality during settlement is a population bottleneck for a tropical surgeonfish. Ecology 85:2422–2428. doi:https://doi.org/10.1890/04-0366
Fishelson L, Popper D, Avidor A (1974) Biosociology and ecology of pomacentrid fishes around the Sinai Peninsula (northern Red Sea). J Fish Biol 6:119–133. doi:https://doi.org/10.1111/j.1095-8649.1974.tb04532.x
Fowler AJ (1990) Validation of annual growth increments in the otoliths of a small, tropical coral reef fish. Mar Ecol Prog Ser 64:25–38. doi:https://doi.org/10.3354/meps064025
Fowler AJ, Doherty PJ (1992) Validation of annual growth increments in the otoliths of two species of damselfish from the Southern Great Barrier Reef. Aust J Mar Freshwater Res 43:1057–1068. doi:https://doi.org/10.1071/MF9921057
Frederick JL (1997) Post-settlement movement of coral reef fishes and bias in survival estimates. Mar Ecol Prog Ser 150:65–74. doi:https://doi.org/10.3354/meps150065
Fricke HW (1980) Control of different mating systems in a coral reef fish by one environmental factor. Anim Behav 28:561–569. doi:https://doi.org/10.1016/S0003-3472(80)80065-0
Hixon MA, Beets JP (1993) Predation, prey refuges, and the structure of coral-reef fish assemblages. Ecol Monogr 63:77–101. doi:https://doi.org/10.2307/2937124
Hixon MA, Jones GP (2005) Competition, predation, and density-dependent mortality in demersal marine fishes. Ecology 86:2847–2859. doi:https://doi.org/10.1890/04-1455
Holbrook SJ, Schmitt RJ (2003) Spatial and temporal variation in mortality of newly settled damselfish: patterns, causes and co-variation with settlement. Oecologia 135:532–541
Holmes TH, McCormick MI (2006) Location influences size-selective predation on newly settled reef fish. Mar Ecol Prog Ser 317:203–209. doi:https://doi.org/10.3354/meps317203
Juanes F (2007) Role of habitat in mediating mortality during the post-settlement transition phase of temperate marine fishes. J Fish Biol 70:661–677. doi:https://doi.org/10.1111/j.1095-8649.2007.01394.x
Karplus I, Katzenstein R, Goren M (2006) Predator recognition and social facilitation of predator avoidance in coral reef fish Dascyllus marginatus juveniles. Mar Ecol Prog Ser 319:215–223. doi:https://doi.org/10.3354/meps319215
Kent R, Holzman R, Genin A (2006) Preliminary evidence on group-size dependent feeding success in the damselfish Dascyllus marginatus. Mar Ecol Prog Ser 323:299–303. doi:https://doi.org/10.3354/meps323299
Kuwamura T, Yogo Y, Nakashima Y (1994) Population-dynamics of goby Paragobiodon echinocephalus and host coral Stylophora pistillata. Mar Ecol Prog Ser 103:17–23. doi:https://doi.org/10.3354/meps103017
Kuwamura T, Nakashima Y, Yogo Y (1996) Plasticity in size and age at maturity in a monogamous fish: effect of host coral size and frequency dependence. Behav Ecol Sociobiol 38:365–370. doi:https://doi.org/10.1007/s002650050253
Lecchini D, Galzin R (2005) Spatial repartition and ontogenetic shifts in habitat use by coral reef fishes (Moorea, French Polynesia). Mar Biol (Berl) 147:47–58. doi:https://doi.org/10.1007/s00227-004-1543-z
Levin PS, Tolimieri N, Nicklin M, Sale PF (2000) Integrating individual behavior and population ecology: the potential for habitat-dependent population regulation in a reef fish. Behav Ecol 11:565–571. doi:https://doi.org/10.1093/beheco/11.5.565
Lewis AR (1997) Recruitment and post-recruit immigration affect the local population size of coral reef fishes. Coral Reefs 16:139–149. doi:https://doi.org/10.1007/s003380050068
Loya Y (1976) Red-Sea coral Stylophora pistillata is a R-strategist. Nature 259:478–480. doi:https://doi.org/10.1038/259478a0
McCormick MI, Makey LJ (1997) Post-settlement transition in coral reef fishes: overlooked complexity in niche shifts. Mar Ecol Prog Ser 153:247–257. doi:https://doi.org/10.3354/meps153247
McCormick MI, Meekan MG (2007) Social facilitation of selective mortality. Ecology 88:1562–1570. doi:https://doi.org/10.1890/06-0830
Nanami A, Nishihira M (2002) The structures and dynamics of fish communities in an Okinawan coral reef: Effects of coral-based habitat structures at sites with rocky and sandy sea bottoms. Environ Biol Fishes 63:353–372. doi:https://doi.org/10.1023/A:1014952932694
Nanami A, Nishihira M (2003) Population dynamics and spatial distribution of coral reef fishes: comparison between continuous and isolated habitats. Environ Biol Fishes 68:101–112. doi:https://doi.org/10.1023/B:EBFI.0000003799.77382.de
Overholtzer-McLeod KL (2004) Variance in reef spatial structure masks density dependence in Coral-Reef fish populations on natural versus artificial reefs. Mar Ecol Prog Ser 276:269–280. doi:https://doi.org/10.3354/meps276269
Overholtzer-McLeod KL (2006) Consequences of patch reef spacing for density-dependent mortality of coral-reef fishes. Ecology 87:1017–1026. doi:https://doi.org/10.1890/0012-9658(2006)87[1017:COPRSF]2.0.CO;2
Sale PF (1972) Influence of corals in the dispersion of the Pomacentrid fish, Dasyllus aruanus. Ecology 53:741–744. doi:https://doi.org/10.2307/1934795
Sandin SA, Pacala SW (2005) Fish aggregation results in inversely density-dependent predation on continuous coral reefs. Ecology 86:1520–1530. doi:https://doi.org/10.1890/03-0654
Shpigel M, Fishelson L (1986) Behavior and physiology of coexistence in 2 species of Dascyllus (Pomacentridae, Teleostei). Environ Biol Fishes 17:253–265. doi:https://doi.org/10.1007/BF00001492
Webster MS (2003) Temporal density dependence and population regulation in a marine fish. Ecology 84:623–628. doi:https://doi.org/10.1890/0012-9658(2003)084[0623:TDDAPR]2.0.CO;2
Wong MYL, Munday PL, Jones GP (2005) Habitat patch size, facultative monogamy and sex change in a coral-dwelling fish, Caracanthus unipinna. Environ Biol Fishes 74:141–150. doi:https://doi.org/10.1007/s10641-005-6715-2
Acknowledgments
Special thanks to R. Niv, O. Polak and N. Ben-Moshe for extensive help UW and to R. Kent, O. Ben-Tzvi and three anonymous reviewers for constructive comments. This research was conducted under permit no. 2007/28847 from the Israeli Nature Reserve Authority. This study was partly supported by the Kreitman foundation.
Author information
Authors and Affiliations
Corresponding author
Additional information
Communicated by S.A. Poulet.
Rights and permissions
About this article
Cite this article
Belmaker, J., Ziv, Y. & Shashar, N. Habitat patchiness and predation modify the distribution of a coral-dwelling damselfish. Mar Biol 156, 447–454 (2009). https://doi.org/10.1007/s00227-008-1098-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00227-008-1098-5