- Open Access
Mismatch between shape changes and ecological shifts during the post-settlement growth of the surgeonfish, Acanthurus triostegus
© Frédérich et al.; licensee BioMed Central Ltd. 2012
- Received: 5 December 2011
- Accepted: 25 April 2012
- Published: 25 April 2012
Many coral reef fishes undergo habitat and diet shifts during ontogeny. However, studies focusing on the physiological and morphological adaptations that may prepare them for these transitions are relatively scarce. Here, we explored the body shape variation related to ontogenetic shifts in the ecology of the surgeonfish Acanthurus triostegus (Acanthuridae) from new settler to adult stages at Moorea Island (French Polynesia). Specifically, we tested the relationship between diet and habitat shifts and changes in overall body shape during the ontogeny of A. triostegus using a combination of geometric morphometric methods, stomach contents and stable isotope analysis.
After reef settlement, stable isotope composition of carbon and nitrogen revealed a change from a zooplanktivorous to a benthic algae diet. The large amount of algae (> 75% of stomach contents) found in the digestive tract of small juveniles (25–30 mm SL) suggested the diet shift is rapid. The post-settlement growth of A. triostegus is highly allometric. The allometric shape changes mainly concern cephalic and pectoral regions. The head becomes shorter and more ventrally oriented during growth. Morphological changes are directly related to the diet shift given that a small mouth ventrally oriented is particularly suited for grazing activities at the adult stage. The pectoral fin is more anteriorely and vertically positioned and its basis is larger in adults than in juveniles. This shape variation had implications for swimming performance, manoeuvrability, turning ability and is related to habitat shift. Acanthurus triostegus achieves its main transformation of body shape to an adult-like form at size of 35–40 mm SL.
Most of the shape changes occurred after the reef colonization but before the transition between juvenile habitat (fringing reef) and adult habitat (barrier reef). A large amount of allometric variation was observed after diet shift from zooplankton to benthic algae. Diet shift could act as an environmental factor favouring or inducing morphological changes. On the other hand, the main shape changes have to be achieved before the recruitment to adult populations and start negotiating the biophysical challenges of locomotion and feeding in wave- and current-swept outer reef habitat.
- Geometric morphometrics
- Habitat change
- Moorea Island
- Reef fishes
Ontogenetic shifts in diet and habitat are the norm for demersal marine fishes. The majority of coral reef fishes have stage-structured life histories with two main distinct stages including a pelagic larval stage capable of long-distance dispersal and a demersal stage (usually juveniles and adults) . The transition from the pelagic oceanic environment to benthic reef environment (i.e. settlement phase) represents a key period, during which fish often undergo a change in form (defined as the combination of size and shape) and physiology to a mode suited for the new environment . The settlement phase may be divided into two parts: (1) the fish’s first association with the reef community and (2) a period when fish change to juvenile form [2, 3]. As fish grow, their morphology, behaviour and sometimes feeding habit change. Accordingly, some studies have investigated the transition from juvenile to adult habitats (i.e. the recruitment phase) [e.g. [2, 4–6]. Four strategies of recruitment according to habitat use were highlighted : (1) an increase in the number of habitats used during the adult stage; (2) a decrease in the number of habitats used by adults compared to recently settled juveniles; (3) the use of different habitat types; and (4) no change in habitat use.
Ecomorphology may assist in our better understanding of the relationships between morphological and ecological changes of an organism during ontogenetic shifts [7, 8]. Most ecomorphological investigations have studied the relationships between ontogenetic diet shifts and the changes in oral anatomy [9–11]. Analyses of covariation between feeding habits and external body shape were successfully applied in marine fish inhabiting coastal waters of Mediterranean seas [12–15] whereas, to our knowledge, ecomorphological studies focusing on the post-settlement ontogeny of coral reef fishes are scarce [for exceptions: [16–18]. Allometry refers to the pattern of covariation between size and shape  and the study of ontogenetic allometry (i.e. the ontogenetic shape changes within a species when size is used as a proxy of developmental age) has provided insight into regularities of size-required changes in shape for the maintenance of function.
In the present study, the post-settlement development of Acanthurus triostegus (L., 1758) was examined. This species is a common coral reef fish in the Indo-Pacific region . In French Polynesia, its larval duration ranges from 44 to 60 days . Typically, juveniles and adults use different habitats . At Moorea Island (Society Archipelago, French Polynesia), A. triostegus larvae colonize the reef at night and directly settle on the beach zone , which is a shallow sandy area with coral slab. When A. triostegus reaches sexual maturity (standard length, SL ≈ 95 mm), they leave the beach community for the barrier reef community where they commonly form large feeding aggregations, which slowly move in the lagoon [5, 20]. It is expected that Acanthurus triostegus also undergo an ontogenetic diet shift. Indeed, A. triostegus is considered as a herbivorous species during its demersal stages , as the majority of Acanthuridae. On the other hand, most surgeonfish larvae feed on planktonic preys such as appendicularians . Studies have not yet explored this diet change and have questioned if this shift is rapid or gradual.
Specifically, the present study explores the diet change and the changes in overall body shape during the post-settlement ontogeny of A. triostegus (i.e. from settling larvae to adult stage). Two approaches were used to explore potential diet change: stomach content and stable isotope analysis. The combination of these methods has the advantage of compensating for the inaccuracy of each method (see  for detailed explanations). Geometric morphometrics was used to study the relationship between body shape variation and changes in feeding habits in a qualitative and quantitative manner. Our approach allowed to highlight a mismatch between morphological changes and ecological shifts in A. triostegus. Indeed a large amount of allometric variation was observed after diet shift from zooplankton to benthic algae but the main shape changes were achieved before the recruitment to adult populations living on the outer reef habitat.
Sampling and data collection
All specimens of Acanthurus triostegus were collected in the lagoon of Moorea Island (17°30’S, 149°50’W; French Polynesia) in October 2009. The sample represented a complete ontogenetic series from larvae (= larvae settling reef) to adult specimens (n = 117; SL, 22.9–153.8 mm). Larvae (n = 17; SL, 24.5–27.3 mm; Additional file 1) were obtained from nets fixed to the reef crest . Fish captured in crest nets during the night were collected at dawn. Juveniles (n = 87; SL, 22.9–61.0 mm) were caught with a Seine net on the beach zone and adults (n = 13; SL, 104.4–153.8 mm) were speared at dusk just behind the reef crest ( Additional file 1 & Additional file 2). After their capture, the fishes were killed as quickly as possible by an overdose immersion in MS-222 then placed on ice.
Different potential primary food sources (plankton and algae) were taken from the fish collection site. Meso-zooplankton was trapped using a net with a mesh of 250 μm, towed on the reef at a 2 m depth. Several samples of filamentous algae colonizing the reef were taken and/or brushed from coral slab and rocks: 5 samples were collected on the juvenile habitat and 3 from the adult habitat (Additional file 2).
A geometric morphometric analysis involves a series of steps, which are briefly described here. The form of an organism is first captured by the Cartesian coordinates of a configuration of anatomical landmarks (Figure 1). The removal of differences in orientation, position, and size allows pure shape to be analyzed. This was achieved in our study by optimally superimposing landmark configurations using a process called generalized Procrustes analysis (GPA), which is based on a least-squares algorithm . During this superimposition, a consensus configuration (average) of landmarks is calculated and will be used as reference. Centroid size (CS) is a measure of the dispersion of landmarks around their centroid and is computed as the square root of the sum of squared distances of all landmarks from the centroid. Although CS was highly related to SL (linear regression: CS = 1.46 SL (mm) – 0.06; r2 = 0.9998, P < 0.001), CS was preferred because this is the only measure of size uncorrelated to shape in the absence of allometry . The new Cartesian coordinates obtained after the superimposition are the Procrustes shape coordinates used for statistical comparisons of individuals. The shape differences between landmark configurations of two individuals can be summarized by their Procrustes distance, which is the square root of the sum of squared distances between pairs of corresponding landmarks. Deformation grids using thin-plate spline (TPS) algorithm are commonly used to visualise the patterns of shape variations [26, 32, 33]. The shape changes modelled by TPS technique can be decomposed into the two components of shape variation, the uniform and non-uniform components. The uniform components (UNI X and UNI Y) express information on global scale shape variation whereas the non-uniform components describe local shape changes at different geometric scales . The first uniform component (UNI X) corresponds to the stretching of a landmark configuration along the x-axis (antero-posterior axis of fish body), whereas the second uniform component (UNI Y) refers to dilatations or compressions along the y-axis (dorso-ventral axis of fish body).
First, correlation analyses were performed between size (ln-CS) and the X and Y uniform components to test ontogenetic shape changes at global scale. Subsequently, a principal component analysis (PCA) was performed on shape data to identify the major axes of ontogenetic shape changes. PCA was performed using PCAGen6 .
Stomachs were opened and their contents visually examined using a Wild M10 binocular microscope following the methodology of Wilson & Bellwood . Gut contents were spread over a Petri dish, covering a 15 × 15 square grid placed underneath. For each of 50 randomly marked grid quadrats, the dominant item (by area) was recorded, along with any other material present in the quadrat. The data were condensed into four categories: benthic algae, benthic invertebrates, zooplankton and detritus. According to Randall , A. triostegus is an herbivorous species at the adult stage. Therefore, we directly calculated the percentage of benthic algae within stomach contents.
Stable isotopes analysis
where X is 13C or 15N and R is the corresponding ratio 13C/12C or 15N/14N for samples or standards. Carbon and nitrogen ratios are expressed relative to the vPDB (Vienna Peedee Belemnite) standard and to atmospheric nitrogen standard, respectively. Reference materials were IAEA-N1 (δ15N = +0.4 ± 0.2‰) and IAEA CH-6 (sucrose) (δ13C = −10.4 ± 0.2‰).
The dynamic of shape changes during ontogeny, expressed as the relationship between PD and CS, is on Figure 2. The trajectory displays an asymptotic curve. The rate of shape changes is high for small individuals and decreases during growth. An adaptive linear regression analysis highlighted a developmental shift for a centroid size value of 5.46, corresponding to 37.8 mm of SL. Consequently, the plateau is reached in the size range of juveniles, revealing that the habitat shift undergone by A. triostegus during the recruitment (i.e. the change from the beach zone to the barrier reef) occurs when all shape changes are almost completed.
There were significant differences between the delta values among settling larvae, juveniles and adult specimens of A. triostegus (Kruskal-Wallis test: δ13C, H2 = 43.96, P < 0.001; δ15N, H2 = 37.93, P < 0.001). Except settling larvae and juveniles showing no difference along the δ15N axis (Dunn’s Multiple comparison test, P > 0.05), all other paired comparisons among groups revealed significant differences (P < 0.001). Adults showed the least negative δ13C values and settling larvae had the most negative δ13C values. Juveniles presented the greater variation of δ13C values. A group of juveniles had very similar δ13C and δ15N values than settling larvae when other juveniles form a group showing a large range of δ13C values. Interestingly, the δ13C variation observed in juveniles is significantly related to fish size (δ13C Vs SL: r2 = 0.26; P < 0.001) and shape (δ13C Vs PC1 r2 = 0.38; P < 0.001). Moreover these linear models fitted better when the five largest juveniles are excluded from the regression analysis (δ13C Vs SL: r2 = 0.62; P < 0.001; δ13C Vs PC1: r2 = 0.47; P < 0.001) (Additional file 3). Settling larvae and adults showed the most positive and the lowest δ15N values, respectively.
For demersal coral reef fishes, there is currently little information connecting morphological changes with ecological changes [e.g. . On the other hand, this kind of data is growing for demersal reef fishes from temperate regions [e.g. [12–15, 37]. Similar to sparids [12, 13, 15] and coral reef damselfishes , the dynamic of shape changes in A. triostegus was asymptotic, reflecting a two-step curve (Figure 2). Acanthurus triostegus achieved their main transformation of body shape to an adult-like form at a size of 35–40 mm SL. Our findings that the mean size of settlement-stage of A. triostegus is 25 mm SL [present study,  and growth rate is a mean of 20 mm SL per month  reveal that the main changes in body shape occur during the first month in the coral reef environment. This stage, corresponding to a shift of allometric pattern, does not coincide with the shift of habitat (Additional file 2, Figure 6). Indeed, the main changes of body shape are completed before the transition from the fringing reef (juvenile habitat) to the reef crest of the barrier reef (adult habitat) , suggesting that fish should acquire a specific body shape to be competitive compared to adults already installed in the reef crest community (Figure 6).
Metamorphosis in fish requires radical changes in external and internal morphology, and is often accompanied by ecological or habitat changes . Generally, metamorphosis is thought to be rapid, usually occurring within a few hours of settlement . Information about metamorphosis in A. triostegus is currently growing. McCormick  highlighted changes in pigmentation and body shape variation in A. triostegus during the first ten days after reef settlement. The main shape changes are a reduction of the second dorsal spine and a reduction of the body depth . After 5 days post-settlement, the mouth starts to move from a terminal to a ventral position . More recently, Frédérich et al. highlighted an unexpected skeletal change during its metamorphosis. They observed a rapid replacement of dermal plates to small scales during the 6–9 days post-settlement. Concerning ecological changes, it is already known that juveniles and adults use different habitat . At Moorea Island, the juveniles of A. triostegus grow on beach zones characterized by a shallow sandy area with coral slab whereas adults inhabit the lagoon to the shoreward side of the barrier reef crest. Our isotopic data clearly demonstrate the ontogenetic diet shift between settling larvae and adults of A. triostegus (Figure 5). Indeed, larvae and adults had δ13C and δ15N values that matched the isotopic signatures of zooplankton and benthic algae, respectively. The size related variation of δ13C observed in juveniles should reflect tissue turnover . Knowing that the small juveniles having similar δ13C and δ15N values than settling larvae already graze filamentous algae revealed the tissue turnover is not instantaneous and some time is needed to reach isotopic equilibrium . On the other hand, the lower values of δ15N observed in adults than in juveniles and their respective algal food sources have to be related to habitat shift and/or the different nutrient sources for benthic algae between juvenile and adult habitats . Indeed, juvenile habitat is close to the beach (our sample site was near a hotel) and an influence of anthropogenic nitrogen inputs on δ15N seems possible . During their pelagic larval phase, A. triostegus feeds on appendicularians and larval polychaetes [20, 22]. Unfortunately, the stomach of all larvae captured during the settlement event was empty. However, benthic algae represented more than 75% of the gut content in all juveniles caught on the beach zone. Knowing that the smallest juveniles caught in the lagoon are similar size to the settling larvae caught using the crest net, suggests the diet change from a planktivorous regime to an herbivorous one should be rapid. Surprisingly, our study reveals that a large amount of allometric shape changes remain to be done after the diet shift has occurred and before the recruitment in adult populations (Figure 6). The quick diet shift after settlement could act as an environmental factor favouring or inducing the main morphological changes at least at the level of the cephalic region. The external morphology of the smallest A. triostegus juveniles would be sufficient for efficient grazing during the first post-settlement days, but the rapid transition to an algivorous regime could also be possible due to physiological adaptations (e.g. new set of digestive enzymes) or morphological adaptations of the digestive tract. In any case, we observed a rapid lengthening of the intestine in A. triostegus juveniles during the first few days post-settlement [Frédérich, pers. obs.]. The timing of metamorphosis in coral reef fishes varies according to fish groups and is directly linked to species-specific ecological transition periods [2, 3]. If the concept of metamorphosis includes the gradual transformations during the juvenile phase, we have demonstrated that A. triostegus achieve their metamorphosis to an adult-like form at a size of 35–40 mm SL (i.e. approximately one month after settlement to the reef).
The allometric shape changes mainly concern the cephalic region and the pectoral region. Conversely, the caudal region did not vary over ontogeny. During growth, the head becomes shorter and more ventrally oriented. The variation of mouth orientation is mainly due to a lengthening of the frontal region and may be correlated with a heightening of the cheeks. These shape changes are directly related to the diet shift. Indeed, a small mouth ventrally oriented is particularly suited for grazing activities at the adult stage [45, 46]. The pectoral fin is more anteriorely and vertically positioned and its basis is larger in adults than in juveniles. This morphological variation of the pectoral region is directly related to ontogenetic habitat shift as suggested by various ecomorphological studies about swimming in coral reef fishes. Juveniles of A. triostegus live a calm inshore environment when adults swim in wave- and current-swept outer reef habitat. Fulton  showed the adults of A. triostegus use essentially their pectoral fins for swimming (Labriform swimming mode sensu  and ) and is one the most powerful swimmers in wave-swept reef crest habitat. Consequently, a larger basis of their pectoral fins observed in adults suggests the development of powerful muscles needed for high swimming speed performance . A more anteriorely positioned pectoral fin in adults is linked to a better ability to break forward movement and thus fine-tune locomotion in quarters of complex substrata . Finally, a more vertically oriented pectoral fin allows a better manoeuvrability and turning ability in adults , another benefit in fast waters and structurally complex environment.
Overall, this study is one of the first to (1) detail quantitatively and qualitatively the complete ontogenetic shape changes of a surgeonfish occurring after reef settlement and to (2) highlight a mismatch between morphological changes and ecological shifts in coral reef fishes. Indeed, a large amount of allometric shape changes remains to be done after the diet shift when most of the shape changes are completed before the second habitat shift from beach zone to barrier reef. Our morphological study shows that cephalic and pectoral regions undergo a large amount of allometric shape changes through post-settlement ontogeny. The number of works focusing on the various modes of post-settlement transition in coral reef fishes is growing [5, 52] but studies investigating the morphological, physiological and ethological adaptations associated to these transition periods are also needed. The magnitude and the disturbance of such adaptations can directly impact levels of mortality occurring at each stage of ontogenetic development after reef settlement.
BF and GL are a Postdoctoral Researcher and a Research Associate of the Fonds National de la Recherche Scientifique of Belgium (F.R.S.-FNRS), respectively. We would like to thank S. Planes, Y. Chancerelle, P. Ung (CRIOBE, Moorea, French Polynesia) for helping to collect the fishes and for providing hospitality and laboratory facilities. The authors thank Sophie Holles for her linguistic assistance. We would like to thank Nicolai Konow and three anonymous reviewers for comments on previous versions of the manuscript. This research was supported by grants from ANR (ANR-06-JCJC-0012-01) and CRISP Program (Coral Reef Initiative in the South Pacific - C2A). This paper is the MARE paper number 226.
- Leis JM, McCormick MI: The biology, behaviour and ecology of the pelagic, larval stage of coral reef fishes. Coral reef fishes: dynamics and diversity in a complex ecosystem. Edited by: Sale PF. 2002, Academic, San Diego, 171-199.View ArticleGoogle Scholar
- McCormick MI, Makey LJ: Post-settlement transition in coral reef fishes: overlooked complexity in niche shifts. Marine Ecology-Progress Series. 1997, 153: 247-257.View ArticleGoogle Scholar
- McCormick MI, Makey L, Dufour V: Comparative study of metamorphosis in tropical reef fishes. Marine Biology. 2002, 141: 841-853. 10.1007/s00227-002-0883-9.View ArticleGoogle Scholar
- Lecchini D: Spatial and behavioural patterns of reef habitat settlement by fish larvae. Marine Ecology-Progress Series. 2005, 301: 247-252.View ArticleGoogle Scholar
- Lecchini D, Galzin R: Spatial repartition and ontogenetic shifts in habitat use by coral reef fishes (Moorea, French Polynesia). Marine Biology. 2005, 147: 47-58. 10.1007/s00227-004-1543-z.View ArticleGoogle Scholar
- Sponaugle S, Cowen RK: Larval supply and patterns of recruitment for two Caribbean reef fishes, Stegastes partitus and Acanthurus bahianus. Marine and Freshwater Research. 1996, 47: 433-447. 10.1071/MF9960433.View ArticleGoogle Scholar
- Norton SF, Luczkovich JJ, Motta PJ: The role of ecomorphological studies in the comparative biology of fishes. Environmental Biology of Fishes. 1995, 44: 287-304. 10.1007/BF00005921.View ArticleGoogle Scholar
- Wainwright PC: Ecological explanation through functional morphology: The feeding biology of sunfishes. Ecology. 1996, 77: 1336-1343. 10.2307/2265531.View ArticleGoogle Scholar
- Eggold BT, Motta PJ: Ontogenetic dietary shifts and morphological correlates in striped mullet, Mugil cephalus. Environmental Biology of Fishes. 1992, 34: 139-158. 10.1007/BF00002390.View ArticleGoogle Scholar
- Luczkovich JJ, Norton SF, Gilmore RG: The Influence of oral anatomy on prey selection during the ontogeny of two percoid fishes, Lagodon rhomboides and Centropomus undecimalis. Environmental Biology of Fishes. 1995, 44: 79-95. 10.1007/BF00005908.View ArticleGoogle Scholar
- Wainwright PC, Richard BA: Predicting patterns of prey use from morphology of fishes. Environmental Biology of Fishes. 1995, 44: 97-113. 10.1007/BF00005909.View ArticleGoogle Scholar
- Loy A, Bertelletti M, Costa C, Ferlin L, Cataudella S: Shape changes and growth trajectories in the early stages of three species of the genus Diplodus (Perciformes, Sparidae). Journal of Morphology. 2001, 250: 24-33. 10.1002/jmor.1056.View ArticlePubMedGoogle Scholar
- Russo T, Costa C, Cataudella S: Correspondence between shape and feeding habit changes throughout ontogeny of gilthead sea bream Sparus aurata L., 1758. Journal of Fish Biology. 2007, 71: 629-656. 10.1111/j.1095-8649.2007.01528.x.View ArticleGoogle Scholar
- Russo T, Pulcini D, Bruner E, Cataudella S: Shape and Size Variation: Growth and Development of the Dusky Grouper (Epinephelus marginatus Lowe, 1834). Journal of Morphology. 2009, 270: 83-96. 10.1002/jmor.10674.View ArticlePubMedGoogle Scholar
- Vigliola L, Harmelin-Vivien M: Post-settlement ontogeny in three Mediterranean reef fish species of the genus Diplodus. Bulletin of Marine Science. 2001, 68: 271-286.Google Scholar
- Frédérich B, Adriaens D, Vandewalle P: Ontogenetic shape changes in Pomacentridae (Teleostei, Perciformes) and their relationships with feeding strategies: a geometric morphometric approach. Biological Journal of the Linnean Society. 2008, 95: 92-105. 10.1111/j.1095-8312.2008.01003.x.View ArticleGoogle Scholar
- Lukoschek V, McCormick MI: Ontogeny of diet changes in a tropical benthic carnivorous fish, Parupeneus barberinus (Mullidae): relationship between foraging behaviour, habitat use, jaw size, and prey selection. Marine Biology. 2001, 138: 1099-1113. 10.1007/s002270000530.View ArticleGoogle Scholar
- Bellwood DR: Ontogenetic changes in the diet of early post-settlement Scarus species (Pisces: Scaridae). Journal of Fish Biology. 1988, 33: 213-219. 10.1111/j.1095-8649.1988.tb05464.x.View ArticleGoogle Scholar
- Klingenberg CP: Heterochrony and allometry: the analysis of evolutionary change in ontogeny. Biological Reviews. 1998, 73: 79-123. 10.1017/S000632319800512X.View ArticlePubMedGoogle Scholar
- Randall JE: A contribution to the biology of the convict surgeonfish of the Hawaiian Islands, Acanthurus triostegus sandoicensis. Pacific Science. 1961, 15: 215-272.Google Scholar
- McCormick MI: Delayed metamorphosis of a tropical reef fish (Acanthurus triostegus): a field experiment. Marine Ecology-Progress Series. 1999, 176: 25-38.View ArticleGoogle Scholar
- Sampey A, McKinnon AD, Meekan MG, McCormick MI: Glimpse into guts: overview of the feeding of larvae of tropical shorefishes. Marine Ecology-Progress Series. 2007, 339: 243-257.View ArticleGoogle Scholar
- Frédérich B, Fabri G, Lepoint G, Vandewalle P, Parmentier E: Trophic niches of thirteen damselfishes (Pomacentridae) at the Grand Récif of Toliara, Madagascar. Ichthyological Research. 2009, 56: 10-17. 10.1007/s10228-008-0053-2.View ArticleGoogle Scholar
- Lecchini D, Dufour V, Carleton J, Strand S, Galzin R: Estimating the patch size of larval fishes during colonization on coral reefs. Journal of Fish Biology. 2004, 65: 1142-1146. 10.1111/j.0022-1112.2004.00493.x.View ArticleGoogle Scholar
- Rohlf FJ: TpsDig (Version 1.40), a software program for landmark data acquisition. 2004, Department of Ecology and Evolution, State University of New York at Stony Brook, doi:, [http://life.bio.sunysb.edu/morph/]Google Scholar
- Bookstein F: Morphometric tools for landmark data: geometry and biology. 1991, University Press, CambridgeGoogle Scholar
- Bookstein F: Combining the tools of geometric morphometrics. Advances in morphometrics. Edited by: Marcus LF, Corti M, Loy A, Naylor G, Slice D. 1996, Plenum Press, New York, 131-151.View ArticleGoogle Scholar
- Rohlf FJ, Marcus LF: A revolution in morphometrics. Trends in Ecology & Evolution. 1993, 8: 129-132. 10.1016/0169-5347(93)90024-J.View ArticleGoogle Scholar
- Zelditch ML, Swiderski DL, Sheets HD, Fink WL: Geometric morphometrics for biologists: A primer. 2004, Elsevier Academic Press, San DiegoGoogle Scholar
- Lawing AM, Polly PD: Geometric morphometrics: recent applications to the study of evolution and development. Journal of Zoology. 2010, 280: 1-7. 10.1111/j.1469-7998.2009.00620.x.View ArticleGoogle Scholar
- Rohlf FJ, Slice D: Extensions of the Procrustes method for the optimal superimposition of landmarks. Systematic Zoology. 1990, 39: 40-59. 10.2307/2992207.View ArticleGoogle Scholar
- Rohlf FJ: Relative warps analysis and an example of its application to mosquito wings. Contributions to morphometrics. Edited by: Marcus LF, Bello E, G-V A. 1993, Monografias del Museo Nacional de Ciencias Naturales, CSIC, Madrid, 131-159.Google Scholar
- Thompson DAW: On growth and form. 1917, Cambridge University Press,View ArticleGoogle Scholar
- Sheets HD: Regress6: calculation of regressions between shape variables and a dependant variable. 2003, Department of Physics, Canisius College, Buffalo, doi:, [http://www2.canisius.edu/~sheets/morphsoft.html]Google Scholar
- Sheets HD: PCAGen6: Principal Component Analysis of shape variables. 2001, Department of Physics, Canisius College, Buffalo, doi:, [http://www2.canisius.edu/~sheets/morphsoft.html]Google Scholar
- Wilson S, Bellwood DR: Cryptic dietary components of territorial damselfishes (Pomacentridae, Labroidei). Marine Ecology-Progress Series. 1997, 153: 299-310.View ArticleGoogle Scholar
- McCormick MI: Ontogeny of diet shifts by a microcarnivorous fish, Cheilodactylus spectabilis: relationship between feeding mechanics, microhabitat selection and growth. Marine Biology. 1998, 132: 9-20. 10.1007/s002270050367.View ArticleGoogle Scholar
- Youson JH: First metamorphosis. Fish physiology. Edited by: Hoar WS, Randall DJ. 1988, Academic, New York, 135-196.Google Scholar
- Victor BC: Settlement strategies and biogeography of reef fishes. The ecology of fishes on coral reefs. Edited by: Sale PF. 1991, Academic, San Diego, 231-260.View ArticleGoogle Scholar
- Frédérich B, Lecchini D, Vandewalle P: Evidence of an original scale development during the settlement phase of a coral reef fish (Acanthurus triostegus). Journal of Applied Ichthyology. 2010, 26: 176-178. 10.1111/j.1439-0426.2010.01399.x.View ArticleGoogle Scholar
- Sweeting CJ, Jennings S, Polunin NVC: Variance in isotopic signatures as a descriptor of tissue turnover and degree of omnivory. Functional Ecology. 2005, 19: 777-784. 10.1111/j.1365-2435.2005.01019.x.View ArticleGoogle Scholar
- Caut S, Angulo E, Courchamp F: Discrimination factors (δ15N and δ13C) in an omnivorous consumer: Effect of diet isotopic ratio. Functional Ecology. 2008, 22: 255-263. 10.1111/j.1365-2435.2007.01360.x.View ArticleGoogle Scholar
- de la Moriniere EC, Pollux BJA, Nagelkerken I, Hemminga MA, Huiskes AHL, van der Velde G: Ontogenetic dietary changes of coral reef fishes in the mangrove-seagrass-reef continuum: stable isotopes and gut-content analysis. Marine Ecology-Progress Series. 2003, 246: 279-289.View ArticleGoogle Scholar
- Lepoint G, Frédérich B, Gobert S, Parmentier E: Isotopic ratios and elemental contents as indicators of seagrass C processing and sewage influence in a tropical macrotidal ecosystem (Madagascar, Mozambique Channel). Scientia Marina. 2008, 72: 109-117.View ArticleGoogle Scholar
- Konow N, Bellwood DR, Wainwright PC, Kerr AM: Evolution of novel jaw joints promote trophic diversity in coral reef fishes. Biological Journal of the Linnean Society. 2008, 93: 545-555. 10.1111/j.1095-8312.2007.00893.x.View ArticleGoogle Scholar
- Purcell SW, Bellwood DR: A functional analysis of food procurement in two surgeonfish species, Acanthurus nigrofuscus and Ctenochaetus striatus (Acanthuridae). Environmental Biology of Fishes. 1993, 37: 139-159. 10.1007/BF00000589.View ArticleGoogle Scholar
- Fulton CJ: Swimming speed performance in coral reef fishes: Field validations reveal distinct functional groups. Coral Reefs. 2007, 26: 217-228. 10.1007/s00338-007-0195-0.View ArticleGoogle Scholar
- Webb PW: The biology of fish swimming. Mechanics and physiology of animal swimming. Edited by: Maddock L, Bone Q, Rayner JMV. 1994, Cambridge University Press, Cambridge, 45-62.View ArticleGoogle Scholar
- Blake RW: Fish functional design and swimming performance. Journal of Fish Biology. 2004, 65: 1193-1222. 10.1111/j.0022-1112.2004.00568.x.View ArticleGoogle Scholar
- Webb PW, LaLiberte GD, Schrank AJ: Does body and fin form affect the maneuverability of fish traversing vertical and horizontal slits?. Environmental Biology of Fishes. 1996, 46: 7-14. 10.1007/BF00001692.View ArticleGoogle Scholar
- Gerstner CL: Maneuverability of four species of coral-reef fish that differ in body and pectoral-fin morphology. Canadian Journal of Zoology. 1999, 77: 1102-1110. 10.1139/z99-086.View ArticleGoogle Scholar
- Nakamura Y, Shibuno T, Lecchini D, Kawamura T, Watanabe Y: Spatial variability in habitat associations of pre- and post-settlement stages of coral reef fishes at Ishigaki Island, Japan. Marine Biology. 2009, 156: 2413-2419. 10.1007/s00227-009-1257-3.View ArticleGoogle Scholar
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