Plasticity of marine sponge habitat preferences with regard to light and water motion: the example of Batzella inops (Topsent, 1891) in submerged caves
P. Nemoy A , E. Spanier A B , N. Kashtan C , A. Israel D and D. L. Angel A B EA The Department of Maritime Civilizations, Leon H. Charney School of Marine Sciences, University of Haifa, Mount Carmel, Haifa 3498838, Israel.
B The Leon Recanati Institute for Maritime Studies, University of Haifa, Mount Carmel, Haifa 3498838, Israel.
C The Department of Conservation Studies, Western Galilee College, Akko 2412101, Israel.
D The National Institute of Oceanography, Israel Oceanographic and Limnological Research, PO Box 8030, Haifa 31080, Israel.
E Corresponding author. Email: dangel@univ.haifa.ac.il
Marine and Freshwater Research 69(11) 1784-1789 https://doi.org/10.1071/MF18001
Submitted: 6 January 2018 Accepted: 2 June 2018 Published: 23 August 2018
Abstract
This study examined the effects of environmental conditions on the distribution of marine sponges. We measured the abundance of the sponge Batzella inops (Topsent, 1891) in two contrasting habitats: inside submerged caves and on the surfaces of submerged boulders. We hypothesised that caves are a preferred habitat for B. inops over the boulder surfaces, and tested this by descriptive (quadrate sampling) and manipulative (reciprocal transplantation) experiments. In addition, we tested B. inops in situ for the presence of photosynthetic activity. We found that B. inops is more abundant inside the caves (mean ± s.e.m., 1.2 ± 0.6 individuals m–2) than on the outside boulder surfaces (0.15 ± 0.19 individuals m–2). We also detected photosynthetic activity in B. inops in both habitats. The results of transplantation experiments suggested that the sponge prefers the transfer from inside to outside the cave rather than vice versa. Therefore, we conclude that although B. inops is more abundant in sheltered habitats, such as submerged caves, adult individuals of this sponge can survive transfer to exposed conditions. Altogether, our findings point to the plasticity of B. inops habitat preferences and may aid further research into conservation or mariculture of this and possibly other sponge species.
Additional keywords: benthos, conservation, ecology, invertebrates.
References
Bakus, G. J. (1990). Marine biological sampling techniques. In ‘Quantitative Ecology and Marine Biology’. pp. 32–47. (Balkema: Rotterdam, Netherlands.)Bannister, R. J., Brinkman, R., Wolff, C., Battershill, C., and de Nys, R. (2007). The distribution and abundance of dictyoceratid sponges in relation to hydrodynamic features: identifying candidates and environmental conditions for sponge aquaculture. Marine and Freshwater Research 58, 624–633.
| The distribution and abundance of dictyoceratid sponges in relation to hydrodynamic features: identifying candidates and environmental conditions for sponge aquaculture.Crossref | GoogleScholarGoogle Scholar |
Beer, S., and Ilan, M. (1998). In situ measurements of photosynthetic irradiance responses of two Red Sea sponges growing under dim light conditions. Marine Biology 131, 613–617.
| In situ measurements of photosynthetic irradiance responses of two Red Sea sponges growing under dim light conditions.Crossref | GoogleScholarGoogle Scholar |
Bell, J. J. (2008). The functional roles of marine sponges. Estuarine, Coastal and Shelf Science 79, 341–353.
| The functional roles of marine sponges.Crossref | GoogleScholarGoogle Scholar |
Bell, J. J., and Barnes, D. K. A. (2000). The distribution and prevalence of sponges in relation to environmental gradients within a temperate sea lough: vertical cliff surfaces. Diversity & Distributions 6, 283–303.
| The distribution and prevalence of sponges in relation to environmental gradients within a temperate sea lough: vertical cliff surfaces.Crossref | GoogleScholarGoogle Scholar |
Bibiloni, M. A., Uriz, M. J., and Gili, J. M. (1989). Sponge communities in three submarine caves of the Balearic Islands (Western Mediterranean): adaptations and faunistic composition. Marine Ecology 10, 317–334.
| Sponge communities in three submarine caves of the Balearic Islands (Western Mediterranean): adaptations and faunistic composition.Crossref | GoogleScholarGoogle Scholar |
Burgsdorf, I., Erwin, P. M., López-Legentil, S., Cerrano, C., Haber, M., Frenk, S., and Steindler, L. (2014). Biogeography rather than association with cyanobacteria structures symbiotic microbial communities in the marine sponge Petrosia ficiformis. Frontiers in Microbiology 5, 529.
| Biogeography rather than association with cyanobacteria structures symbiotic microbial communities in the marine sponge Petrosia ficiformis.Crossref | GoogleScholarGoogle Scholar |
Bussotti, S., Terlizzi, A., Fraschetti, S., Belmonte, G., and Boero, F. (2006). Spatial and temporal variability of sessile benthos in shallow Mediterranean marine caves. Marine Ecology Progress Series 325, 109–119.
| Spatial and temporal variability of sessile benthos in shallow Mediterranean marine caves.Crossref | GoogleScholarGoogle Scholar |
Corriero, G., Liaci, S., Ruggiero, D., and Pansisni, M. (2000). The sponge community of a semi-submerged Mediterranean cave. Marine Ecology 21, 85–96.
| The sponge community of a semi-submerged Mediterranean cave.Crossref | GoogleScholarGoogle Scholar |
Doty, M. S. (1971). Measurement of water movement in reference to benthic algal growth. Botanica Marina 14, 32–35.
| Measurement of water movement in reference to benthic algal growth.Crossref | GoogleScholarGoogle Scholar |
Gerovasileiou, V., and Voultsiadou, E. (2012). Marine caves of the Mediterranean Sea: a sponge biodiversity reservoir within a biodiversity hotspot. PLoS One 7, e39873.
| Marine caves of the Mediterranean Sea: a sponge biodiversity reservoir within a biodiversity hotspot.Crossref | GoogleScholarGoogle Scholar |
Gerovasileiou, V., Chintiroglou, C. C., Konstantinou, D., and Voultsiadou, E. (2016). Sponges as ‘living hotels’ in Mediterranean marine caves. Scientia Marina 80, 279–289.
| Sponges as ‘living hotels’ in Mediterranean marine caves.Crossref | GoogleScholarGoogle Scholar |
Gunasekera, S. P., McCarthy, P. J., Longley, R. E., Pomponi, S. A., Wright, A. E., Lobkovsky, E., and Clardy, J. (1999). Discorhabdin P, a new enzyme inhibitor from a deep-water Caribbean sponge of the genus Batzella. Journal of Natural Products 62, 173–175.
| Discorhabdin P, a new enzyme inhibitor from a deep-water Caribbean sponge of the genus Batzella.Crossref | GoogleScholarGoogle Scholar |
Harmelin, J. G. (1997). Diversity of bryozoans in a Mediterranean sublittoral cave with bathyal-like conditions: role of dispersal processes and local factors. Marine Ecology Progress Series 153, 139–152.
| Diversity of bryozoans in a Mediterranean sublittoral cave with bathyal-like conditions: role of dispersal processes and local factors.Crossref | GoogleScholarGoogle Scholar |
Konstantinou, D., Gerovasileiou, V., Voultsiadou, E., and Gkelis, S. (2018). Sponges–cyanobacteria associations: global diversity overview and new data from the eastern Mediterranean. PLoS One 13, e0195001.
| Sponges–cyanobacteria associations: global diversity overview and new data from the eastern Mediterranean.Crossref | GoogleScholarGoogle Scholar |
Lemloh, M. L., Fromont, J., Brümmer, F., and Usher, K. M. (2009). Diversity and abundance of photosynthetic sponges in temperate Western Australia. BMC Ecology 9, 4.
| Diversity and abundance of photosynthetic sponges in temperate Western Australia.Crossref | GoogleScholarGoogle Scholar |
Maldonado, M., Giraud, K., and Carmona, C. (2008). Effects of sediment on the survival of asexually produced sponge recruits. Marine Biology 154, 631–641.
| Effects of sediment on the survival of asexually produced sponge recruits.Crossref | GoogleScholarGoogle Scholar |
Mariani, S., Uriz, M. J., Turon, X., and Alcoverro, T. (2006). Dispersal strategies in sponge larvae: integrating the life history of larvae and the hydrologic component. Oecologia 149, 174–184.
| Dispersal strategies in sponge larvae: integrating the life history of larvae and the hydrologic component.Crossref | GoogleScholarGoogle Scholar |
Meroz-Fine, E., Shefer, S., and Ilan, M. (2005). Changes in morphology and physiology of an East Mediterranean sponge in different habitats. Marine Biology 147, 243–250.
| Changes in morphology and physiology of an East Mediterranean sponge in different habitats.Crossref | GoogleScholarGoogle Scholar |
Morley, S. A., Berman, J., Barnes, D. K., de Juan Carbonell, C., Downey, R. V., and Peck, L. S. (2016). Extreme phenotypic plasticity in metabolic physiology of Antarctic demosponges. Frontiers in Ecology and Evolution 3, 157.
| Extreme phenotypic plasticity in metabolic physiology of Antarctic demosponges.Crossref | GoogleScholarGoogle Scholar |
Newman, D. J., and Cragg, G. M. (2016). Natural products as sources of new drugs from 1981 to 2014. Journal of Natural Products 79, 629–661.
| Natural products as sources of new drugs from 1981 to 2014.Crossref | GoogleScholarGoogle Scholar |
Preciado, I., and Maldonado, M. (2005). Reassessing the spatial relationship between sponges and macroalgae in sublittoral rocky bottoms: a descriptive approach. Helgoland Marine Research 59, 141–150.
| Reassessing the spatial relationship between sponges and macroalgae in sublittoral rocky bottoms: a descriptive approach.Crossref | GoogleScholarGoogle Scholar |
Steindler, L., Beer, S., Peretzman-Shemer, A., Nyberg, C., and Ilan, M. (2001). Photoadaptation of zooxanthellae in the sponge Cliona vastifica from the Red Sea, as measured in situ. Marine Biology 138, 511–515.
| Photoadaptation of zooxanthellae in the sponge Cliona vastifica from the Red Sea, as measured in situ.Crossref | GoogleScholarGoogle Scholar |
Steindler, L., Beer, S., and Ilan, M. (2002). Photosymbiosis in intertidal and subtidal tropical sponges. Symbiosis 33, 263–273.
Steindler, L., Schuster, S., Ilan, M., Avni, A., Cerrano, C., and Beer, S. (2007). Differential gene expression in a marine sponge in relation to its symbiotic state. Marine Biotechnology 9, 543–549.
| Differential gene expression in a marine sponge in relation to its symbiotic state.Crossref | GoogleScholarGoogle Scholar |
Topsent, E. (1891). Essai sur la faune des spongiaires de Roscoff. Archives de Zoologie Expérimentale et Générale 9, 533–534.
Uriz, M. J., Rosell, D., and Martin, D. (1992). The sponge population of the Cabrera Archipelago (Balearic Islands): characteristics, distribution, and abundance of the most representative species. Marine Ecology 13, 101–117.
| The sponge population of the Cabrera Archipelago (Balearic Islands): characteristics, distribution, and abundance of the most representative species.Crossref | GoogleScholarGoogle Scholar |
Van Soest, R. W. M. (2002). Family Chondropsidae Carter, 1886. In ‘Systema Porifera: A Guide to the Classification of Sponges’. (Eds J. N. A. Hooper and R. W. M. Van Soest.) pp. 521–527. (Kluwer Academic/Plenum Publishers: New York, NY, USA.)
Voultsiadou, E. (2009). Reevaluating sponge diversity and distribution in the Mediterranean Sea. Hydrobiologia 628, 1–12.
| Reevaluating sponge diversity and distribution in the Mediterranean Sea.Crossref | GoogleScholarGoogle Scholar |
Wilkinson, C. R., and Vacelet, J. (1979). Transplantation of marine sponges to different conditions of light and current. Journal of Experimental Marine Biology and Ecology 37, 91–104.
| Transplantation of marine sponges to different conditions of light and current.Crossref | GoogleScholarGoogle Scholar |
Wulff, J. (2012). Ecological interactions and the distribution, abundance, and diversity of sponges. Advances in Marine Biology 61, 273–344.
| Ecological interactions and the distribution, abundance, and diversity of sponges.Crossref | GoogleScholarGoogle Scholar |