Suberitidae (Demospongiae, Hadromerida) From
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Beaufortia INSTITUTE OF TAXONOMIC ZOOLOGY (ZOOLOGICAL MUSEUM) UNIVERSITY OF AMSTERDAM Vol. 43 no. 11 December 31, 1993 Suberitidae (Demospongiae, Hadromerida) from the North Aegean Sea EleniVoultsiadou-Koukoura.*& Rob W. M. van Soest** *Department University ofThessaloniki, 54006 Thessaloniki, Greece **Institute of Taxonomic (Zoological Museum), University ofAmsterdam, P.O.Box 94766, 1090 GTAmsterdam, TheNetherlands Keywords: Sponges, Hadromerida, Suberitidae, North Aegean Sea Abstract Sampling in the North Aegean Sea yielded nine species of the family Suberitidae, four of which, Pseudosuberites sulphureus, P. Suberiles for the fauna ofthe Eastern and three hyalinus, ficus and S. syringella, are new Mediterranean, more, S. carnosus, S. and S. records for the fauna of the Sea. For each of the nine the domuncula, massa, are new Aegean species comments on systematics, as well as geographical and ecological informationis given. A redescription is given of the littleknown species Suberites massa Nardo. A review ofthe distributionof all Mediterranean Suberitidae is also presented, in which it is con- in materialhave been from the Eastern cluded that a further three species not represented our reported Mediterranean, and P. the viz. Laxosuberites ectyoninus, Prosuberites longispina, epiphytum. Six suberitids reported from other parts of Mediterra- nean so far have not been found in the Eastern Mediterranean. INTRODUCTION siadou-Koukoura, et al. 1991; Voultsiadou- Koukoura & Van Soest 1991a,b; Voultsiadou- of Eastern Mediterranean is Koukoura & the results of the Knowledge sponges Koukouras, 1993), that of other of the Med- have been and are poor compared to parts sponge collecting being re- iterranean Van 1994: Recent several science and (cf. Soest, Fig. 2). ported; species new to appar- collecting activities in the North Aegean Sea ently endemic to the Eastern Mediterranean been of have been described. have organized especially for the purpose of The increasing this knowledge, and thus enabling present paper deals with the Hadromerid Eastern Suberitidae. five more firmly based conclusions on alleged family Thusfar, only species of Mediterranean endemism and generally low di- this family were reported from Greek waters: In Voult- versity. an ongoing series of papers (e.g. Rhizaxinella pyrifera (Delia Chiaje), Terpios fugax 176 & Duch. Mich., Laxosuberites ectyoninus Topsent, fined a separate family Polymastiidae as having Prosuberites longispina Topsent and P. epiphytum a differentiated cortex and a radiating skeleton). (Lamarck). From other Eastern Mediterranean Lévi "Hadromerida (1973): ... without digitate localities also Suberites domuncula (Olivi) (Sea of papillae. The skeleton, often confused in the in- S. Marmara and Black Sea), carnosus (Johnston) terior, is generally radiating at the periphery." Nardo (Suez Canal) and S.massa (Sea of Marma- (translated from French) (Lévi defined a separate ra) were recorded. family Polymastiidae as having "...generally two The of this is three of ...with purpose paper to give new syste- or categories tylostyles; digitate matic, ecological and zoogeographical informa- erect papillae..."). the the and of the tion on Suberitidae of Aegean Sea Bergquist (1978): "...radial arrangement more generally of the Eastern Mediterranean, as skeleton is evident only at the surface. The spi- of of have in the well as an account the distribution the spe- cules confused orientation deeper re- in in cies belonging to this family the Mediterrane- gions of the sponges, but a few cases may as- an. sume a loose axial orientation." (Bergquist defin- ed a separate family Polymastiidae as having MATERIALAND METHODS "..tylostyles... always divisible into two or three clear size Microscleres but categories. are rare, A total of 105 specimens were examined, collect- acanthose micro-oxeas can be present. The ed from various localities in the North Aegean ...body with erect oscular and pore-bearing papil- Sea. Sampling was made by SCUBA diving, lae is characteristic for the family"). fishing nets, dredges and grabs, in depths from 3 Hartman (1982) follows Bergquist's definition to about 150 m. The examined material is de- closely, but assigns spined centrotylote diactinal posited in the Museum of the Department of Zo- "microscleres" to the suberitids instead of to the ology, University of Thessaloniki and partly in polymastiids. the Zoological Museum of Amsterdam. By comparing the various definitions of the fami- SYSTEMATIC REMARKS AND DESCRIP- ly Suberitidae, there are few definite characters TIONS by which it can be identified without referring to the Polymastiidae: Suberitidae do not have pa- Family Suberitidae Schmidt, 1870 pillae (but some Polymastiidae such as certain Aaptos species, also lack them, while other non- Remarks on the definition of the family, includ- polymastiid Hadromerids, like Cliona, sometimes brief of its and its distinct- have there should be cortical ing a survey history, papillae), no spe- from is ness the closely related family Polymastii- cialization (but it as yet unclear to which ex- Suberiti- in other than dae Gray, 1867, which shares with the tent that exists genera Polymastia) dae the absence of aster- or streptaster micro- and no clear megasclere size categories are al- scleres: lowed (but Suberites species frequently have a " Schmidt (1870): without special cortical clearly smaller tylostyle size in the peripheral The character all authors structures.... spicules in confusion or in reticulate bouquets). only agree directed is the confused of the choanosomal tracts.... spicules in the periphery out- upon nature wards..." from in- however the skeletons of (translated German) (Schmidt skeleton; e.g. Rhizaxinella of Suberites described be- cludes Radiella and part of the Polymastia species, spp., and also that massa in axial which are now grouped in the family Polymastii- low, are well organized an skeleton of dae ). aligned larger tylostyles and an extra-axial skele- Topsent (1900): "Clavulida normally without ton of radiating bundles of smaller tylostyles. We differentiated radiat- with that the Sube- microscleres; no cortex; no agree Boury-Esnault (1987) in ing skeleton. Megascleres almost constantly ty- ritidae-Polymastiidae are need of a critical re- lostyles." (translated from French) (Topsent de- vision. 177 The following nine suberitid species, belonging to thors) that the Mediterranean and North Atlan- four found in the collected material: tic of the genera were specimens present species are conspecif- ic with the South Atlantic ones remains to be Genus Pseudosuberites Topsent, 1893 demonstrated. Several specimens described from the Mediterranean have considerably smaller spi- Suberitidae with tangential Halichondria-like de- cules than the maximum given by Ridley & tachable ectosomal skeleton, covering large sub- Dendy (1100 by 25 pm) and Topsent (1900) dermal spaces; choanomal skeleton also a Hali- (1200 by 26 pm), viz. Vacelet (1969): 660 by 22 chondria-like On confused mass of tylostyles (re- pm, Pulitzer-Finali (1983): 810 by 17 pm. the phrased after Topsent, 1900). other hand, specimens described by Uriz (1988) from deep water off Namibia, show considerably Pseudosuberites sulphureus (Bowerbank, bigger spicules (up to 2030 pm ). 1866) Genus Terpios Duchassaing & Michelotti, 1864 Suberanthusflavus;Von Lendenfeld, 1896: 144, pl. V, VII, XII (not: Halichondriaflava Lieberkiihn, 1859). "Thinly encrusting Suberitidae with gelatinous choanosome containing small tylostyles in disor- Two specimens were collected on the coast of the derly arrangement" (Topsent, 1900)(translated Sithonia Peninsula (Singitikos Bay), at a depth of from French). 4 attached coral Cladocora Remark: There has been m, to a colony of the a tendency among au- thors - - confine caespitosa. The morphology and skeletal structure probably unwarranted to the use conform to Topsent's (1900) description; tylos- of Terpios to thinly encrusting suberitids with measured 300-500 4-12 De tyles x (im. poly-lobate tylostyle heads (cf. Laubenfels, in in The species was not previously found the 1936:152), order to avoid confusion with Pro- Eastern Mediterranean, but it has been widely suberites (encrusting Suberitidae with tylostyles in the with reported elsewhere, both the Mediterranean erect on substrate points outward), and (e.g. Topsent, 1925; Pulitzer-Finali, 1983) and Laxosuberites (encrusting or massive Suberitidae on the Eastern Atlantic coasts (e.g. Topsent, with the tylostyles arranged in radiating tracts P. be confused with P. mollis in surface defined 1900). sulphureus may ending bouquets) (both as by Topsent (1925, 1934); the spiculeso f this West- Topsent, 1900). However, Terpios, Prosuberites and Mediterranean Laxosuberites characters in various ern species, however, are appre- seem to occur ciably smaller and thinner (up to 365 by 8 pm). combinations in different species. For example the Indo-West Pacific species “Suberites” cruciatus Pseudosuberites hyalinus (Ridley & Dendy, Dendy has the quadrilobate tylostyle-heads of 1887) Terpios combined with a Laxosuberites architec- A ture. revision of encrusting suberitids might re- Six in veal specimens were collected Thermaikos and that the differences between these "genera" and off Pagasitikos Bays the coasts of Lesbos Is- are artificial. of 60 - 150 rocks and land, at depths m, on co- ralligenous substrates. The morphology and skel- Terpios fugax Duchassaing & Michelotti, etal structure conform to Topsent's (1900) 1864 descriptions; the fusiform tylostyles