Student no.: 610026241 The use of nursery habitats by Haemulon sciurus, Chromis cyanea and Thalassoma bifasciatum in the Bahamas Summary The use of so-called ‘nursery habitats’ such as mangroves and seagrass meadows is an important part of early development for many coral-reef species, including in the Bahamas. The degree of use of these back-reef systems, as well as by which species, can vary and understanding the differences is vital to informing policy on specially designated Marine Protected Areas (MPAs). Here we show that two species, Haemulon sciurus and Thalassoma bifasciatum, use the mangroves of San Salvador, but not the seagrass meadows, as nursery habitats. A third species, Chromis cyanea, was not found to use either as nursery habitats. Summary word count: 98 Introduction Coral-reef inhabiting fish have long been known to utilise ‘nursery habitats’ as safe environments for juvenile development, considered important to many Caribbean species1. Specifically, mangroves and seagrasses serve as intermediary habitats2, providing maximum food availability and minimum predation risk in order to allow a variety of species to grow and develop with minimal stressors3. This nursery role of back-reef systems has only recently begun to be properly understood4. Indeed, it has been found that proximity of coral reef fish communities to nursery habitats greatly increases the biomass of these species, even outweighing the benefits of no-take Marine Protected Areas (MPAs) 5, in addition to strongly impacting community structure on the reef2. The assemblages of species inhabiting seagrass beds and mangroves vary, with different species inhabiting one or both of these habitatswith mangroves in particular exclusively containing several juvenile species3. With anthropogenic activity threatening the stability and preservation of nursery habitats, the importance of understanding which species utilise these environments, and to what extent, is greater than ever. Mangroves, for example, are among the most threatened coastal biotypes6 whilst also one of the most important. We studied three coral-reef fish species - Haemulon scirus (Blue-striped Grunt), Chromis cyanea (Blue Chromis) and Thalassoma bifasciatum (Blue-headed Wrasse) – on the Bahamian island of San Salvador. Their sizes were measured over three different habitats of coral reef, seagrass and mangroves, to determine whether these species utilised the back-reef systems as nurseries. It was expected that all three would be found to use at least one back-reef environment as a nursery for the smaller, juvenile stages, in agreement with previous observations of some of these species in the area of San Salvador7 and the Bahamas8. Methods Line transects of 30m x 2m, the exact position of which chosen randomly, were run at each of the three different habitats. Several different sites were used for each habitat and the results pooled together to give a more complete representation of each of the three habitat types on the island. Numbers of each of the three studied fish species and their estimated Student no.: 610026241 length were recorded by visual census along each line. Length was estimated as 0-5cm, 510cm, 10-15cm, etc. and then assigned a value of 3cm, 8cm, 13cm etc. respectively. For the mangrove habitat, transects were run along the tree line and the visual census completed by looking into the root systems. Surveys were carried out during the same week in June 2013, between 8am and 5pm. Average size and standard deviation were then calculated for each fish species at each site, and a single factor ANOVA test was carried out to determine whether or not the differences in average fish size, for each species, between the habitats was significant. Results The average size of T.bifasciatum (fig.1) was found to be smallest in the mangrove habitat (5.07cm) than the reef habitat (6.59cm), with the differences in sizes between the three areas found to be significant (p=0). The size variation of H.sciurus (fig.2) was found to follow a similar pattern, with the mangrove population appearing significantly smaller (6.26cm) than the reef populations (9.16cm); size differences between all three habitats were again significant (p=0). For both T. bifasciatum and H. sciurus, seagrass populations were found to be, on average, the largest. Data for C. cyanea was only available for reef populations, as none of this particular species were seen in either seagrass or mangrove habitats during the visual surveys. Standard deviation is used for all data sets, as it refers to individual and separate data sets. Fig. 1 12 10 Mean Size (cm) 8 6 4 2 0 Reef Seagrass Mangrove Habitat Type Mean Size (cm) Fig. 2 16 14 12 10 8 6 4 2 0 Reef Seagrass Habitat Type Mangrove Student no.: 610026241 Fig. 3 Habitat Type Reef Seagrass Mangroves T. bifasciatum 3518 48 544 Number of Individuals (n) H. sciurus 2482 5 614 C. cyanea 194 0 0 Figure Legends Figure 1 – Mean size of T. bifasciatum in Reef and Back-reef habitats - A bar graph showing the mean size of T. bifasciatum (Blue-headed Wrasse), in cm, over the three different habitats surveyed. P=0 (<0.05). Error bars represent standard deviation (SD=3.88, 2.07 & 0.8 respectively). Figure 2 – Mean size of H. sciurus in Reef and Back-reef habitats - A bar graph showing the mean size of H. sciurus (Blue-striped Grunt), in cm, over the three different habitats surveyed. P=0 (<0.05). Error bars represent standard deviation (SD=6, 2.74 & 2.91 respectively). Figure 3 – Individuals of species surveyed – A table to show the total number of individuals (n) recorded in each of three habitat types surveyed. Discussion Both T. bifasciatum and H. sciurus can be determined to use the mangroves of San Salvador as nursery habitats, with the average size of both species significantly smaller at the mangrove site than on the reef sites (fig. 1 & fig. 2). This conforms to expectations, as well as previous findings both on San Salvador in regards to H. sciurus7 and to reefs more generally for most fish species. Perhaps unexpectedly, these two species were found overall to be larger in the seagrass habitat. There are, however, several potential reasons for this. Most importantly, the sample sizes of species seen in the seagrass habitat were very small (fig. 3). This could be due to experimental error – the seagrass beds were much deeper than the other habitats when surveyed, with identification of fish therefore much more difficult if they were hiding amongst the seagrass. However, it may be that these fish do not use this Student no.: 610026241 environment as a nursery habitat at all but instead solely as feeding grounds. Indeed, the importance of seagrass meadows does appear to vary with a number of factors – whilst juvenile survival in seagrass habitats tends to be greater when compared to unstructured habitats9, structured mangrove habitats are much more preferred10. Our visual surveys only recorded the presence of C. cyanea in reef environments. The overwhelming lack of C. cyanea at the back-reef systems would seem to strongly indicate that this species does not use the seagrass or mangrove habitats as nurseries. As there is little literature on this species’ juvenile stage, it is hard to compare to any previous findings - though our initial hypothesis presumed that this species would have showed similar patterns to the other two species studied. Planktivores such as C. cyanea form an important trophic link between reef and open-water communities11, and as such further investigation of C. cyanea’s juvenile habitats is important for better understanding of much wider interactions and trophic interactions. Whilst the data presented here should be expanded upon by further study to potentially improve the accuracy, it provides a firm basis from which decisions can begin to be made regarding local habitat protection. The use of nursery habitats by H. sciurus and T. bifasciatum on San Salvador may be indicative of much wider use by other species, including those considered more economically or culturally important to the local area. Therefore, these results should be used primarily as a starting point in the on-going discussion regarding the future of Marine Protected Areas on the island. Word count:1,000 References 1. Nagelkerken, I., et al. Dependence of Caribbean reef fishes on mangroves and seagrass beds as nursery habitats: a comparison of fish faunas between bays with and without mangroves/seagrass beds. Marine Ecology Progress Series 214, 225-235 (2001). 2. Mumby, P.J., et al. Mangroves enhance the biomass of coral reef fish communities in the Caribbean. Nature 427, 533-536 (2004). 3. Laegdsgaard, P., Johnson, C. Why do juvenile fish utilise mangrove habitats? Journal of Experimental Marine Biology and Ecology 257, 229-253 (2011). 4. Adams, A.J., et al. Nursery function of tropical back-reef systems. Marine Ecology Progress Series 318, 287-301 (2006). 5. Nagelkerken, I., Grol, M.G.G., Mumby, P.J. Effects of Marine Reserves versus Nursery Habitat Availability of Reef Fish Communities. PLoS ONE 7(6) (2012). 6. Layman, C.A., Arrington, D.A., Kramer, P.A., Valentine-Rose, L., Dahlgren, C.P. Indicator Taxa to Assess Anthropogenic Impacts in Caribbean and Bahamas Tidal Creeks. Caribbean Journal of Science 46(1), 12-18 (2010). 7. Conboy, I.C., Haynes, J.M. Potential of Pigeon Creek, San Salvador, Bahamas, as Nursery Habitat for Juvenile Reef Fish. The International Journal of Bahamian Studies 17(2). http://journals.sfu.ca/cob/index.php/files/article/view/138 (2011). Student no.: 610026241 8. Layman, C.A., Silliman, B.R. Preliminary Survey and Diet Analysis of an Estuarine Creek on Andros Island, Bahamas. Bulletin of Marine Science 70(1), 199-210 (2002). 9. Heck Jr, K.L., Hays, G., Orth, R.J. Critical evaluation of the nursery role hypothesis for seagrass meadows. Marine Ecology Progress Series 253, 123-136 (2003). 10. Laegdsgaard, P., Johnson, C.R. Mangrove habitats as nurseries: unique assemblages of juvenile fish in subtropical mangroves in eastern Australia. Marine Ecology Progress Series 126, 67-81 (1995). 11. Harborne, A.R., et al. Tropical Coastal Habitats as Surrogates of Fish Community Structure, Grazing, and Fisheries Value. Ecological Applications 18(7), 1689-1701 (2008).