Patterns of Association between Marine Sponges and the Associated Organisms: Case Study, Losin Island, Pattani, Thailand

Authors

  • Udomsak DARUMAS Division of Biology, School of Science, Walailak University, Nakhon Si Thammarat 80160, Thailand
  • Supaporn PHASOMBUN Division of Biology, School of Science, Walailak University, Nakhon Si Thammarat 80160, Thailand
  • Ratchanee PUTTAPREECHA Marine and Coastal Resources Research and Development Center Lower Gulf of Thailand, Songkhla 90100, Thailand

DOI:

https://doi.org/10.48048/wjst.2020.5151

Keywords:

Chondrilla, Cinachyrella, Hyrtios, Xestospongia, Gap, Overgrown, Overgrow, Tissue contact

Abstract

Ko Losin, the southernmost offshore islet in the Gulf of Thailand is one of the most naturally, less anthropogenic disturbed coral reefs in Thailand and the home of the major sessile organisms: corals and sponges. This study aims to investigate the natural patterns of association (interactions) between marine sponges and the associated organisms. The types of interaction were classified into 4 categories: Gap, Overgrown, Tissue contact, and Overgrow. The investigation focused on four genera of sponges: Chondrilla, Hyrtios, Cinachyrella, and Xestospongia. Chondrillid sponge showed the high frequency of inhabiting associated organisms. Some hermatypic corals such as Montiporian corals and Porites corals were highly proportioned to the associated organisms. The gap and overgrown interactions were recorded in this study.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Author Biographies

Udomsak DARUMAS, Division of Biology, School of Science, Walailak University, Nakhon Si Thammarat 80160, Thailand

Division of Biology

Supaporn PHASOMBUN, Division of Biology, School of Science, Walailak University, Nakhon Si Thammarat 80160, Thailand

Biology

References

MC Diaz and K Rützler. Sponges: an essential component of Caribbean coral reefs. Bull. Mar. Sci. 2001; 69, 535-46.

TH Suchanek, RC Carpenter, JD Witman and CD Harvell. Sponges as important space competitors in deep Caribbean coral reef communities. Ecol. Deep Shallow Coral Reefs 1983; 7, 55-60.

LAM Aerts and RWMV Soest. Quantification of sponge/coral interactions in a physically stressed reef community, NE Colombia. Mar. Ecol. Prog. Ser. 1997; 148, 125-34.

EL McLean and PM Yoshioka. Association and Interactions between Gorgonians and Sponges. In: MR Custódio, G Lobo-Hajdu, E Hajdu and G Muricy (Eds.). Porifera Research: Biodiversity, Innovation and Sustainability. Museu Nacional de Rio de Janeiro, Brasil, 2007, p. 443-8.

AL Powell, LJ Hepburn, DJ Smith and JJ Bell. Patterns of sponge abundance across a gradient of habitat quality in the Wakatobi Marine Park, Indonesia. Open Mar. Biol. J. 2010; 4, 31-8.

J Lam, YW Cheng, WNU Chen, HH Li, CS Chen and SE Peng. A detailed observation of the ejection and retraction of defense tissue acontia in sea anemone (Exaiptasia pallida). J. Life Environ. Sci. 2017; 5, e2996.

M López-Victoria, S Zea and E Weil. Competition for space between encrusting excavating Caribbean sponges and other coral reef organisms. Mar. Ecol. Prog. Ser. 2006; 312, 113-21.

JE García-Hernández, GWNM van Moorsel and BW Hoeksema. Lettuce corals overgrowing tube sponges at St. Eustatius, Dutch Caribbean. Mar. Biodivers. 2017; 47, 55-6.

CG Easson, M Slattery, DM Baker and DJ Gochfeld. Complex ecological associations: Competition and facilitation in sponge-algal interaction. Mar. Ecol. Prog. Ser. 2014; 507, 153-67.

JR Pawlik. The chemical ecology of sponges on caribbean reefs: Natural products shape natural systems. BioScience 2011; 61, 888-98.

F Azzini, B Calcinai, C Cerrano, G Bavestrello and M Pansini. Sponges of the Marine Karst Lakes and of the Coast of the Islands of Ha Long Bay (North Vietnam). In: MR Custodia, G Lobo-Hajdu, E Hajdu and G Muricy (Eds.). Porifera Research: Biodiversity Innovation and Sustainability. Museu Nacional de Rio de Janeiro, Brasil, 2007, p. 157-64.

E Mclean, K Rützler and P Pooler. Competing for space: Factors that lead to sponge overgrowth when interacting with octocoral. Open J. Mar. Sci. 2015; 5, 64-80.

K Ruetzler. Sponges on coral reefs: A community shaped by competitive cooperation. Bollettino dei Museidegli Istitute Biologici dell’ Universita di Genova 2004; 68, 85-148.

NE Chadwick and KM Morrow. Competition among Sessile Organisms on Coral Reefs. In: Z Dubinsky and N Stambler (Eds.). Coral Reefs: An Ecosystem in Transition. Springer, Dordrecht, Netherlands, 2011, p. 347-71.

J Wulff. Ecological Interactions and the distribution, abundance, and diversity of sponges. Adv. Mar. Biol. 2012; 61, 273-344.

M López-Victoria and S Zea. Storm-mediated coral colonization by an excavating Caribbean sponge. Clim. Res. 2004; 26, 251-6.

NJ de Voogd, LE Becking, BW Hoeksema, A Noor and RWMV Soest. Sponge interactions with spatial competitors in the Spermonde Archipelago. Bollettino dei Musei e degli Istituti Biologici dell Universita di Genova 2004; 68, 253-61.

PK Dayton. Competition, disturbance, and community organization: The provision and subsequent utilization of space in a rocky intertidal community. Ecol. Monogr. 1971; 41, 351-89.

DE Goldberg and K Landa. Competitive effect and response: Hierarchies and correlated trairs in the early stages of competition. J. Ecol. 1991; 79, 1013-30.

JG Puntieri and P Pysek. Branching and competitive hierarchies in populations of Galiun aparine. Can. J. Bot. 1998; 76, 63-74.

MH Gu, T Wang and ZK Xie. Competitive hierarchy among three perennial grasses under clipping and fertilization through three growing years on the eastern Qinghai-Tibetan Plateau. Proc. Environ. Sci. 2012; 13, 151-7.

KE Buenau, NN Price and RM Nisbet. Size dependence, facilitation, and microhabitats mediate space competition between coral and crustose coralline algae in spatially explicit model. Ecol. Model. 2012; 273-238, 23-33.

KRN Anthony, JA Maynard, G Diaz-Pulido, PJ Mumby, PA Marshall, L Cao and O Hoegh-Guldberg. Ocean acidification and warming will lower coral reef resilience. Global Change Biol. 2011; 17, 1798-808.

SK Roth, A Powell, DJ Smith, F Roth and B Schierwater. The highly competitive ascidian Didemnum sp. threatens coral reef communities in Wakatobi Marine National Park, Southern Sulawesi, Indonesia. Regin. Stud. Mar. Sci. 2018; 24, 48-54.

ICS Cruz, LG Water, RKP Kikuchi, ZMAN Leão and A Turra. Marginal coral reefs show high susceptibility of phase shift. Mar. Pollut. Bull. 2018; 135, 551-61.

ICS Cruz, VH Meira, RKP de Kikuchi and JC Creed. The role of competition in the phase shift to dominance of the zoanthid Palythoa cf. variabilis on coral reefs. Mar. Environ. Res. 2016; 115, 28-35.

T-L Loh and JR Pawlik. Chemical defenses and resource trade-offs structure sponge communities on Caribbean coral reefs. Proc. Natl. Acad. Sci. 2014; 111, 4151-6.

Downloads

Published

2020-05-19

How to Cite

DARUMAS, U. ., PHASOMBUN, S. ., & PUTTAPREECHA, R. . (2020). Patterns of Association between Marine Sponges and the Associated Organisms: Case Study, Losin Island, Pattani, Thailand. Walailak Journal of Science and Technology (WJST), 17(6), 514–528. https://doi.org/10.48048/wjst.2020.5151