Order VERONGIIDA Bergquist, 1978


Compiler and date details

2010 - John Hooper, Queensland Museum, Brisbane

 

Diagnosis

Demospongiae where in the anastomosing skeleton the meshes are polygonal, and there is no distinction between primary ascending and secondary connecting elements. Fibres can become organised into a single plane either throughout the sponge or as lamellae near the surface; occasionally intertwined fascicles of fibres emphasise such surface specialisation. The typical fibre structure is a markedly concentric laminar bark surrounding a pith of
fine fibrillar material. Both bark and pith elements can be reduced and both can be almost lost in some genera, but traces always remain. Fibrous spicules separate from the main skeleton and composed only of bark elements can occur. The boundary between bark and pith is very marked, and the fibres on drying appear hollow. Cellular elements (degenerative spongocytes) become incorporated in the fibres in one family. Fibres rarely contain foreign detritus. Choanocyte chambers are diplodal or eurypylous and the mesohyl matrix, in which many different cell types are represented, is densely infiltrated by fibrillar collagen. A collagenous ectosome is usually differentiated and achieves a tissue-like construction with dense aggregations of spherulous cells. The texture of verongiid sponges reflects the collagenous nature of the matrix, they are homogeneous, deformable and fleshy. A very common pigmentation is sulphur yellow tinged with green; on death or damage this oxidises rapidly to dark brown, or more frequently deep purple, almost black. Some show differential surface/internal pigmentation in life. Verongiids range in form from tall tubular vases to thin spreading crusts, some degree of stalk formation is common. The mode of reproduction is oviparous; the structure of the larvae is unknown. Verongida are extremely distinct biochemically. They have no terpenes, but a lipid fraction high in sterol within which novel aplystane sterols frequently dominate. Tyrosinederived brominated compounds occur in all genera that have been studied.

 

ID Keys

KEY TO FAMILIES
(1) Choanocyte chambers eurypylous -------------------------------------------------------------------------- Ianthellidae
Choanocyte chambers diplodal -------------------------------------------------------------------------------------------------- 2

(2) Fibrous skeleton reticulate ------------------------------------------------------------------------------------ Aplysinidae
Fibrous skeleton dendritic -------------------------------------------------------------------------------------------------------- 3

(3) Bark elements absent from fibres ------------------------------------------------------------------ Pseudoceratinidae
Bark and pith elements both present in fibres --------------------------------------------------------------- Aplysinellidae

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Order Verongida Bergquist, 1978. 1081 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1081]

 

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Family ERNSTILLIDAE Vacelet et al., 2019

 

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DEMOSPONGIAE Sollas, 1885 09-Aug-2021 ADDED

Genus Ernstilla Vacelet et al., 2019

 

Distribution

States

Northern Territory, Queensland, Western Australia


IMCRA

Northern Shelf Province (25), Northwest Shelf Transition (26), Northwest Shelf Province (27)

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Species Ernstilla lacunosa (Hentschel, 1912)

 

Generic Combinations

 

Distribution

States

Northern Territory, Queensland, Western Australia


Extra Distribution Information

From the Gulf of Carpentaria QLD, to Exmouth Gulf WA.


IMCRA

Northern Shelf Province (25), Northwest Shelf Transition (26), Northwest Shelf Province (27)

Distribution References

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Family APLYSINELLIDAE Bergquist, 1980


Compiler and date details

2010 - John N.A. Hooper, Queensland Museum, Brisbane, Queensland, Australia

 

Introduction

The Aplysinellidae Bergquist, 1980, are verongids with dendritic skeleton made up of fibres with both bark and pith elements represented, both components can vary in the relative proportion of the fibre section that they constitute. Some species exhibit a different surface to interior pigmentation in life which remains discernable in alcohol, this is unusual within the Verongida. Free fibrous spicules augment the fibre skeleton in one genus (Aplysinella). Fibre mass in relation to soft tissue volume varies from strongly fibrous (Porphyria), to predominance of collagenous matrix (Suberea). Choanocyte chambers are diplodal, small and spherical.

Three genera are included with distribution from the Red Sea, Indo-Pacific, Australian tropical and warm temperate regions. Several species now grouped within Aplysina and Pseudoceratina need to be transferred to aplysinellid genera, mainly to Suberea, but there is need for a comprehensive revision. Nine species are currently described in the family (Bergquist & Cook 2002).

 

Diagnosis

Verongida with dendritic skeleton made up of fibres with both bark and pith elements represented, both components can vary in the relative proportion of the fibre section that they constitute Some species exhibit a different surface to interior pigmentation in life which remains discernable in alcohol, this is unusual within the Verongida. Free fibrous spicules augment the fibre skeleton in one genus (Aplysinella). Fibre mass in relation to soft tissue volume varies from strongly fibrous (Porphyria), to predominance of collagenous matrix (Suberea). Choanocyte chambers are diplodal, small and spherical.

 

ID Keys

KEY TO GENERA
(1) Fibre skeleton includes free fibrous spicules --------------------------------------------------------------- Aplysinella
Fibrous spicules absent --------------------------------------------------------------------------------------------------------- 2

(2) Fibre skeleton strongly represented, bark dominant in fibres -------------------------------------------- Porphyria
Fibre skeleton sparse, pith dominant in fibres --------------------------------------------------------------------- Suberea

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplyinellidae Bergquist, 1980. pp. 1094-1096 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1094]

 

General References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplyinellidae Bergquist, 1980. pp. 1094-1096 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1.

 

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Genus Aplysinella Bergquist, 1980

 

Distribution

States

Queensland


IMCRA

Central Eastern Shelf Transition (39), Northeast Shelf Province (40), Northeast Shelf Transition (41)

Diagnosis

Aplysinellidae with differential pigmentation in life between surface and interior, fibres of characteristic construction having both bark and pith components, the latter being dominant, and fibre skeleton augmented by strongylote fibrous spicules. The spicules are composed only of bark and have a clear axial canal.

 

ID Keys

See Family Aplysinellidae Diagnosis.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplyinellidae Bergquist, 1980. pp. 1094-1096 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1095]

 

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Species Aplysinella rhax (Laubenfels, 1954)

 

Distribution

States

Queensland


IMCRA

Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Aquatic, coral reef, filter-feeder.

 

General References

Hooper, J.N.A., List-Armitage, S.E., Kennedy, J.A., Cook, S.D. & Valentine, C.A. 1999. Sponges of the Low Isles, Great Barrier Reef: an important scientific site, or a case of mistaken identity? Memoirs of the Queensland Museum 44: 249-262 [260] (Listed in this article)

Nevalainen, T.J., Quinn, R.J. & Hooper, J.N.A. 2004. Phospholipase A2 in Porifera. Comparative Biochemistry and Physiology 137(B): 413-420 [415] (Listed in this article)

 

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Species Aplysinella strongylata Bergquist, 1980

 

Distribution

States

Queensland


IMCRA

Central Eastern Shelf Transition (39), Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Aquatic, coral reef, filter-feeder.

 

General References

Hooper, J.N.A. & Kennedy, J.A. 2002. Small-scale patterns of sponge biodiversity (Porifera) on Sunshine Coast reefs, eastern Australia. Invertebrate Systematics 16(4): 637-653 [640]

 

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Genus Suberea Bergquist, 1995

 

Distribution

States

New South Wales, Queensland, Victoria, Western Australia


IMCRA

Southwest Shelf Transition (30), Southwest Shelf Province (31), Western Bass Strait Shelf Transition (34), Central Eastern Shelf Province (38), Northeast Shelf Province (40)

Diagnosis

Aplysinellidae with coarse irregular dendritic fibres in which bark and pith elements are present but the pith predominates. The bark is strongly laminated and very brittle. Fibres can be very thick and render the texture of the sponge interior very rough to the touch. Dense collagen reinforces the matrix, making the sponges hard, to just compressible. The surface is smooth or conulose and the sponge form massive, sometimes stalked or branching. With the addition of the species referred below, there are eight described species of Suberea.

 

ID Keys

See Family Aplysinellidae Diagnosis.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplyinellidae Bergquist, 1980. pp. 1094-1096 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1096]

 

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Species Suberea clavata (Pulitzer-Finali, 1982)

 

Distribution

States

Queensland


Extra Distribution Information

Known only from type locality.


IMCRA

Northeast Shelf Province (40)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth 8–12 m.

 

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Species Suberea fusca (Carter, 1880)

 

Distribution

States

Western Australia


IMCRA

Southwest Shelf Transition (30), Southwest Shelf Province (31)

Ecological Descriptors

Aquatic, benthic, filter-feeder.

 

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Species Suberea ianthelliformis (Lendenfeld, 1888)

 

Distribution

States

New South Wales, Victoria


IMCRA

Western Bass Strait Shelf Transition (34), Central Eastern Shelf Province (38)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth 52 m.

 

General References

Wiedenmayer, F. 1989. Demospongiae (Porifera) from northern Bass Strait (Shelf of Southern Australia). Memoirs of Museum Victoria 50(1): 1-242 [154]

 

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Family APLYSINIDAE Carter, 1875


Compiler and date details

John N.A. Hooper, Queensland Museum, Brisbane, Queensland, Australia; Felix Wiedenmayer (1994), Naturhistorisches Museum Basel, Basel, Switzerland; updated by John N.A. Hooper (1999)

Introduction

The Aplysinidae Carater, 1875, are verongids with an anastomosing skeleton of polygonal meshes which have no tendency to be organised in one plane. The fibres have normal bark and pith elements, contain no foreign detritus and are of moderately even dimensions throughout the sponge. The choanocyte chambers are diplodal, small, and spherical, and are set in a dense collagenous matrix. All species display a marked oxidative colour change at death or on exposure to air, quickly changing from the normal yellow or yellow-green through blue to dark brown or purple. Pigmentation, other than superficial casts attributable to cyanobacteria, is uniform throughout the sponge. Secondary metabolites include a range of brominated tyrosine derivatives with strong antimicrobial activity, similar and often identical structures occur in the Aplysinellidae, Druinellidae and Ianthellidae, they thus characterise the order Verongida. A range of aplystane sterols also characterise the Aplysinidae, and Druinellidae. The sponges are oviparous, and, while extrusion of gametes has been observed, no larvae have been described.

The Aplysinidae is a cohesive group, like other verongiid families it is sharply distinct from other fibrous Porifera. The characteristics of the skeleton, defined precisely, are distinctive and knowledge of ultrastructural histology, biochemistry and reproductive pattern when considered together testify to the long independent evolution of this group of taxa.

Two established genera are included, Aplysina and Verongula, with Aiolochroia also included as incertae sedis within Verongida and suspected affinities to this family. Distribution is Caribbean and Mediterranean predominantly. Records from Red Sea, Indian Ocean, West Central Pacific, Australia and West coast of North America all need to be verified as it is likely that the species in question belong either to the Pseudoceratinidae or Aplysinellidae (Bergquist & Cook 2002).

 

Diagnosis

Verongida with an anastomosing skeleton of polygonal meshes which have no tendency to be organised in one plane. The fibres have normal bark and pith elements, contain no foreign detritus and are of moderately even dimensions throughout the sponge. The choanocyte chambers are diplodal, small, and spherical, and are set in a dense collagenous matrix. All species display a marked oxidative colour change at death or on exposure to air,
quickly changing from the normal yellow or yellow-green through blue to dark brown or purple. Pigmentation, other than superficial casts attributable to cyanobacteria, is uniform throughout the sponge. Secondary metabolites include a range of brominated tyrosine derivatives with strong antimicrobial activity, similar and often identical structures occur in the Aplysinellidae, Druinellidae and Ianthellidae, they thus characterise the order Verongida. A
range of aplystane sterols also characterise the Aplysinidae, and Druinellidae. The sponges are oviparous, and, while extrusion of gametes has been observed, no larvae have been described.

 

ID Keys

KEY TO GENERA
(1) Sponge surface smooth, even, finely conulose ------------------------------------------------------------------- Aplysina
Sponge surface thrown into low folds producing a honeycomb-like appearance ------------------------------- Verongula
Surface with rounded tubercles surrounding depressions to give an overall polygonal appearance -------Aiolochroia

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplysinidae Carter, 1875. pp. 1082-1085 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1082]

 

General References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplysinidae Carter, 1875. pp. 1082-1085 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1.

 

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Genus Aplysina Nardo, 1834

 

Taxonomic Decision for Synonymy

 

Distribution

States

New South Wales, Queensland, Victoria, Western Australia


Extra Distribution Information

Amphi-Atlantic, Mediterranean Sea, Red Sea, Indian Ocean, Indo-Malayan region, E Pacific and Antarctic.


IMCRA

Central Western Shelf Transition (28), Central Western Shelf Province (29), Western Bass Strait Shelf Transition (34), Bass Strait Shelf Province (35), Southeast Shelf Transition (37), Central Eastern Shelf Province (38), Northwest Province (4), Northeast Shelf Province (40), Northeast Shelf Transition (41), Central Western Transition (5)

Diagnosis

Aplysinidae characterised by possession of fibres of only one kind with no foreign detritus and having a thick pith component. The fibres form a regular reticulum with large polygonal meshes and no specialised surface arrangement. Sixty three species have been described under the names Aplysina and Verongia. Many of these will prove to be synonyms but re-examination is difficult since dry material yields little information and for many species no material at all has survived.

 

ID Keys

See Family Aplysinidae Diagnosis.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Aplysinidae Carter, 1875. pp. 1082-1085 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1082]

 

General References

Wiedenmayer, F. 1977. Shallow-water Sponges of the Western Bahamas. Basel : Birkhäuser (Experientia Suppl. 28) 287 pp. 43 pls.

 

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Species Aplysina cacos Lendenfeld, 1888

 

Distribution

States

New South Wales


IMCRA

Southeast Shelf Transition (37), Central Eastern Shelf Province (38)

Ecological Descriptors

Filter-feeder, marine, sessile.

 

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Species Aplysina compacta Carter, 1881

 

Distribution

States

Western Australia


Extra Distribution Information

Known only from type locality.


IMCRA

Central Western Shelf Transition (28), Central Western Shelf Province (29), Northwest Province (4), Central Western Transition (5)

Ecological Descriptors

Filter-feeder, marine, sessile.

 

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Species Aplysina higginsii Lendenfeld, 1889

 

Distribution

Extra Distribution Information

'Australian Seas'.

Known only from type locality.


Ecological Descriptors

Filter-feeder, marine, sessile.

 

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Species Aplysina laevis Carter, 1885

 

Distribution

States

New South Wales, Victoria


Extra Distribution Information

Durras and Port Phillip.


IMCRA

Western Bass Strait Shelf Transition (34), Bass Strait Shelf Province (35), Southeast Shelf Transition (37), Central Eastern Shelf Province (38)

Ecological Descriptors

Filter-feeder, marine, sessile.

 

General References

Capon, R.J. & MacLeod, J.K. 1987. Two epimeric dibromo nitriles from the Australian sponge Aplysina laevis. Australian Journal of Chemistry 40: 341-346 [341]

 

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Species Aplysina lendenfeldi Bergquist, 1980

 

Distribution

States

New South Wales, Victoria


IMCRA

Western Bass Strait Shelf Transition (34), Bass Strait Shelf Province (35), Southeast Shelf Transition (37)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth 10–30 m.

 

General References

Wiedenmayer, F. 1989. Demospongiae (Porifera) from northern Bass Strait (Shelf of Southern Australia). Memoirs of Museum Victoria 50(1): 1-242 [155]

 

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Species Aplysina minima Hentschel, 1914

 

Distribution

Extra Distribution Information

Aust. Antarctic Terr., Heard Is.; off Wilhelm II Coast, Enderby Land and Antarctic.


Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Subtidal–385 m.

 

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Species Aplysina mollis Row, 1911

 

Taxonomic Decision for Subspecies Arrangement

 

Distribution

States

Queensland


IMCRA

Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Benthic, filter-feeder, sessile.

 

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Subspecies Aplysina mollis aruensis Hentschel, 1912

 

Distribution

States

Queensland


IMCRA

Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Benthic, filter-feeder, marine, sessile.

Extra Ecological Information

Depth 15–31 m.

 

General References

Burton, M. 1934. Sponges. Scientific Reports of the Great Barrier Reef Expedition 1928-1929 4: 513-621 pls 1-2

 

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Family IANTHELLIDAE Hyatt, 1875


Compiler and date details

2010 - John N.A. Hooper, Queensland Museum, Brisbane, Queensland, Australia; Felix Wiedenmayer (1994), Naturhistorisches Museum Basel, Basel, Switzerland; updated by John N.A. Hooper (1999)

Introduction

Among the family Ianthellidae Hyatt, 1875, lobate and fan-shaped, stalked growth forms are common. Pigmentation ranges from typically verongid sulphur yellow, deep orange to deep purple, and all show the characteristic oxidation reaction upon damage or death, eventually turning deep purple. The fibre skeleton, where present, is reticulate and frequently compressed into two dimensions, radiating from the contracted basal attachment. Fibres may attain large sizes, particularly towards the base of the sponge, and contain cellular elements in distinctive concentric annuli occurring mainly in the bark component of each fibre. Choanocyte chambers are large and eurypylous, sac-shaped, varying between genera from simply elongate to occasionally branched.

Three genera are recognised in the family, all restricted to relatively shallow waters (Hartman 1982). All three genera are represented in the Australian fauna (Bergquist 1980; Bergquist & Kelly-Borges 1995).

Biochemical characteristics of Ianthellidae are similar to those of the Aplysinidae with respect to the occurrence of brominated metabolites. No aplystane sterols have yet been recorded in any species of Ianthellidae, whereas these sterols characterise the Aplysinidae and Druinellidae, which are almost identical in their major biochemical characteristics (Bergquist 1980).

The Ianthellidae (which includes Bajalidae Lévi, 1958 in synonymy) is reviewed in Bergquist (1980), and the genus Ianthella in Bergquist & Kelly-Borges (1995).

 

Diagnosis

Verongida in which the fibre skeleton when present is strongly anastomosing, frequently compressed into two dimensions, and radiating from a contracted base of attachment. Fibres contain cellular elements in concentric annuli; these occur mainly in bark elements, but can also be dispersed in pith as well. The fibres are of typical construction for the order with bark and pith elements represented, neither component is emphasised. Individual fibres can attain great thickness, particularly towards the base of the sponge. The skeleton makes up the major bulk of the sponge. A thick firm skin-like dermis is common to all species as is the inclusion of spherulous cells among the secretory cell content. The choanocyte chambers are large, and sac-shaped (Ianthella, Hexadella), to slightly ovate-elongate and occasionally branched (Anomoianthella). Colour in life ranges from sulphur yellow through deep orange, blue to deep purple or purple brown. All species show a characteristic oxidation reaction upon damage or death, and reach a final deep purple colouration. Soft tissue pigmentation is always uniform throughout the sponge. Biochemical characteristics are similar to those of the Aplysinidae, Pseudoceratinidae and Aplysinellidae with respect to the occurrence of brominated metabolites but highly complex variants of these molecules occur in the Ianthellidae. No aplystane sterols are known from any species of Ianthellidae.

 

ID Keys

KEY TO GENERA
(1) Fibre skeleton present ------------------------------------------------------------------------------------------------------- 2
Fibre skeleton absent ----------------------------------------------------------------------------------------------- Hexadella

(2) Fibre reticulation two dimensional sometimes with fasciculate extensions vertical to that plane ------- Ianthella
Fibre reticulation anastomosing in three dimensions ---------------------------------------------------- Anomoianthella

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Ianthellidae Hyatt, 1875. pp. 1089-1093 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1089]

 

General References

Bergquist, P.R. 1980. A revision of the supraspecific classification of the orders Dictyoceratida, Dendroceratida and Verongida (Class Demospongiae). New Zealand Journal of Zoology 7: 443-503 figs 1-25 pls

Bergquist, P.R. 1995. Dictyoceratida, Dendroceratida and Verongida from the New Caledonia Lagoon (Porifera: Demospongiae). Memoirs of the Queensland Museum 38(1): 1-51

Bergquist, P.R. & Cook, S.D.C. 2002. Family Ianthellidae Hyatt, 1875. pp. 1089-1093 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1.

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176

Hartman, W.D. 1982. Porifera. pp. 640-666 in Parker, S.P. (ed.). Synopsis and Classification of Living Organisms. New York : McGraw-Hill Vol. 1.

 

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Genus Anomoianthella Bergquist, 1980

 

Distribution

States

Western Australia


Extra Distribution Information

Western Australia.


IMCRA

Central Western Shelf Province (29), Southwest Shelf Transition (30), Southwest Shelf Province (31)

Diagnosis

Ianthellidae with thickened fan-, club-, or cup-shaped growth form, with discrete oscular and poral surface or localised oscular regions. The sponge is cavernous, with extremely thick fibres which form an irregular three dimensional anastomosing reticulum, soft tissue is sparse in relation to fibrous material. The fibres have substantial pith and a bark component in which numerous degenerate spongocytes are arranged in concentric annuli. The choanocyte chambers are eurypylous elongate-oval and sometimes branched.

 

ID Keys

See Family Ianthellidae Diagnosis.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Ianthellidae Hyatt, 1875. pp. 1089-1093 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1091]

 

General References

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176 [151] (relationship to Ianthella)

 

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Species Anomoianthella popeae Bergquist, 1980

 

Distribution

States

Western Australia


Extra Distribution Information

Known only from type locality.


IMCRA

Southwest Shelf Transition (30)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth 4–8 m.

 

General References

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176 [151] (generic comparison with Ianthella spp.)

 

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Genus Ianthella Gray, 1869

 

Taxonomic Decision for Synonymy

 

Distribution

States

New South Wales, Northern Territory, Queensland, Western Australia


Extra Distribution Information

Indian Ocean and Indo-Malayan region.


IMCRA

Timor Transition (1), Tasmania Province (10), Southeast Transition (11), Central Eastern Province (12), Tasman Basin Province (13), Central Eastern Transition (15), Kenn Transition (16), Kenn Province (17), Northeast Province (18), Northeast Transition (19), Timor Province (2), Cape Province (20), Northern Shelf Province (25), Northwest Shelf Transition (26), Northwest Shelf Province (27), Central Western Shelf Transition (28), Central Western Shelf Province (29), Northwest Transition (3), Southwest Shelf Transition (30), Southwest Shelf Province (31), Southeast Shelf Transition (37), Central Eastern Shelf Province (38), Central Eastern Shelf Transition (39), Northwest Province (4), Northeast Shelf Province (40), Northeast Shelf Transition (41), Central Western Transition (5)

Distribution References

Diagnosis

Planar skeleton, degenerate spongocytes arranged in concentric layers within bark, extending to pith regions as dispersed cells. Sponges are large fans or vases, up to 2m high and brightly coloured. The skeleton makes up the bulk of the sponge body and can be a rectangular reticulation of fascicles crosslinked by secondary fibres, or a simple reticulation of anastomosing fibres, developed in two dimensions. Fibre outgrowths at right angles to the basic two dimensional reticulum are present in several species. The choanosome is cavernous with large, sacshaped eurypylous choanocyte chambers. The mesohyl of the choanosome is usually lightly to moderately collagen reinforced, but the ectosomal region has strong collagen deposition. Sponges are yellow, green, orange, blue and purple in colour.

 

ID Keys

See Family Ianthellidae Diagnosis.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Ianthellidae Hyatt, 1875. pp. 1089-1093 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1090]

 

General References

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176 [151]

 

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12-Feb-2010 (import)

Species Ianthella basta (Pallas, 1766)

 

Distribution

States

Northern Territory, Queensland, Western Australia


Extra Distribution Information

Torres Strait, N Great Barrier Reef; also Papua New Guinea, New Caledonia, Guam, Mascarene Islands, Indian Ocean.


IMCRA

Timor Transition (1), Northern Shelf Province (25), Northwest Shelf Transition (26), Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Aquatic, filter-feeder, sessile.

 

General References

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176 [152]

Franklin, M.A., Penn, S.G., Lebrilla, C.B., Lam, T.H., Pessah, I.N. & Molinski, T.F. 1996. Bastadin 20 and bastadin O-sulfate esters from Ianthella basta — novel modulators of the Ry(1)R FKBP12 receptor complex. Journal of Natural Products 59: 1121-1127 [1121]

Fromont, J. 2003. Porifera (Sponges) in the Dampier Archipelago: Taxonomic affinities and biogeography. Proceedings of the Twelfth International Marine Biological Workshop. The Marine Flora and Fauna of Dampier, Western Australia. 405-417 pp. [408] (Listed in this article)

Hooper, J.N.A., Kennedy, J.A., List-Armitage, S.E., Cook, S.D. & Quinn, R. 1999. Biodiversity, species composition and distribution of marine sponges in Northeast Australia. Memoirs of the Queensland Museum 44: 263-274 [264]

Hooper, J.N.A., List-Armitage, S.E., Kennedy, J.A., Cook, S.D. & Valentine, C.A. 1999. Sponges of the Low Isles, Great Barrier Reef: an important scientific site, or a case of mistaken identity? Memoirs of the Queensland Museum 44: 249-262 [260] (Listed in this article)

Pitcher, C.R., Wassenberg, T.J., Smith, G.P., Cappo, M., Hooper, J.N.A. & Doherty, P.J. 1999. Innovative new methods for measuring the natural dynamics of some structurally dominant tropical sponges and other sessile fauna. Memoirs of the Queensland Museum 44: 479-484 [483] (Listed in this article)

Webster, N.S. 2007. Sponge disease: a global threat ? Environmental Microbiology 9(6): 1363-1375 [1366]

 

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Species Ianthella flabelliformis (Pallas, 1766)

 

Distribution

States

New South Wales, Northern Territory, Queensland, Western Australia


Extra Distribution Information

Penguin Channel, Torres Strait, Port Jackson, Hawksbury Rive; also southern Papua New Guinea.


IMCRA

Central Western Shelf Transition (28), Central Western Shelf Province (29), Southeast Shelf Transition (37), Central Eastern Shelf Province (38), Northwest Province (4), Northeast Shelf Province (40), Northeast Shelf Transition (41), Central Western Transition (5)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth 8–51 m.

 

General References

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176 [155]

Fromont, J. 2003. Porifera (Sponges) in the Dampier Archipelago: Taxonomic affinities and biogeography. Proceedings of the Twelfth International Marine Biological Workshop. The Marine Flora and Fauna of Dampier, Western Australia. 405-417 pp. [409] (Listed in this article)

Hooper, J.N.A., List-Armitage, S.E., Kennedy, J.A., Cook, S.D. & Valentine, C.A. 1999. Sponges of the Low Isles, Great Barrier Reef: an important scientific site, or a case of mistaken identity? Memoirs of the Queensland Museum 44: 249-262 [260] (Listed in this article)

 

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Species Ianthella homei Gray, 1869

 

Distribution

Extra Distribution Information

Exact locality unknown.

Known only from type locality.


Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Unknown.

 

General References

Bergquist, P.R. 1980. A revision of the supraspecific classification of the orders Dictyoceratida, Dendroceratida and Verongida (Class Demospongiae). New Zealand Journal of Zoology 7: 443-503 figs 1-25 pls [443] (unrecognisable)

Bergquist, P.R. & Kelly-Borges, M. 1995. Systematics and biogeography of the genus Ianthella (Demospongiae: Verongida: Ianthellidae) in the South-west Pacific. The Beagle, Records of the Museums and Art Galleries of the Northern Territory 12: 151-176 [151] (declared unrecognisable)

 

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Species Ianthella labyrinthus Bergquist & Kelly-Borges, 1995

 

Distribution

States

Northern Territory, Western Australia


Extra Distribution Information

Buccaneer Archipelago, NW Australia.


IMCRA

Timor Transition (1), Northern Shelf Province (25), Northwest Shelf Transition (26), Northwest Shelf Province (27)

Ecological Descriptors

Aquatic, filter-feeder, sessile.

Extra Ecological Information

35 m depth; sand covered rock.

 

General References

Fromont, J. 2003. Porifera (Sponges) in the Dampier Archipelago: Taxonomic affinities and biogeography. Proceedings of the Twelfth International Marine Biological Workshop. The Marine Flora and Fauna of Dampier, Western Australia. 405-417 pp. [409] (Listed in this article)

 

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Species Ianthella quadrangulata Bergquist & Kelly-Borges, 1995

 

Distribution

States

New South Wales, Queensland, Western Australia


Extra Distribution Information

Port Jackson, Sydney, Port Stephens, Illawarra, Lord Howe Is., NSW; Perth region, Frankland Islands, WA; Mooloolaba, Moreton Bay, QLD.


IMCRA

Tasmania Province (10), Southeast Transition (11), Central Eastern Province (12), Tasman Basin Province (13), Northwest Shelf Province (27), Central Western Shelf Province (29), Southwest Shelf Transition (30), Southwest Shelf Province (31), Southeast Shelf Transition (37), Central Eastern Shelf Province (38), Central Eastern Shelf Transition (39), Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Aquatic, filter-feeder, sessile.

 

General References

Hooper, J.N.A. & Kennedy, J.A. 2002. Small-scale patterns of sponge biodiversity (Porifera) on Sunshine Coast reefs, eastern Australia. Invertebrate Systematics 16(4): 637-653 [640] (Listed in this article)

Nevalainen, T.J., Quinn, R.J. & Hooper, J.N.A. 2004. Phospholipase A2 in Porifera. Comparative Biochemistry and Physiology 137(B): 413-420 [416] (Listed in this article)

 

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Species Ianthella reticulata Bergquist & Kelly-Borges, 1995

 

Distribution

States

Queensland


Extra Distribution Information

Davies Reef, Pandora Reef, Russell Is., Escape Reef, QLD; also Bootless Bay, Aidler's Bay, Port Moresby region, and Madang, Papua New Guinea.


IMCRA

Central Eastern Shelf Transition (39), Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Aquatic, filter-feeder, sessile.

Extra Ecological Information

Inshore fringing reef and slopes; 10–20 m depth.

 

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Species Ianthella topsenti (Sollas, 1903)

 

Distribution

States

Queensland


Extra Distribution Information

Torres Strait.


IMCRA

Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Unknown.

 

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Family PSEUDOCERATINIDAE Carter, 1885


Compiler and date details

2010 - John N.A. Hooper, Queensland Museum, Brisbane, Queensland, Australia

Introduction

The Pseudoceratinidae Carter, 1885 (formerly Druinellidae Lendenfeld, 1889) include sponges in which the fibre skeleton, which is sparse, is dendritic, is made up of fibres with no investing bark, simply pith elements which are usually clear, but which occasionally can incorporate isolated fragments of debris. The fibres are extremely irregular, knotted in places, expanding and contracting along their length and below the surface fanning out in brushes. Pigmentation is uniform throughout the sponge, the surface is conulose and the texture rubbery, flexible in ramose forms, tending to incompressible in massive species.

Four nominal genera are included in the family (sensu Bergquist & Cook 2002), of which only one is considered to be valid.

Bergquist et al. (1991) initially suggested biochemical heterogeneity between species of Druinella, Psammaplysilla and Pseudoceratina, based on sterol composition, indicated that the latter two genera should be included in a separate family (Aplysinellidae Bergquist, 1980), leaving only Druinella in the Druinellidae (=Pseudoceratinidae). Morphological differences that supported sterol characteristics consisted of a dendritic dense skeleton in the Druinellidae, where fibres have knotted irregular interlacing protuberances of the bark component (Bergquist et al. 1991), whereas in Apysinellidae pith elements are present in fibres sometimes to the exclusion of bark (Bergquist 1980). Later (Bergquist 1995) synonymised all three genera, and in the most recent revision (Bergquist & Cook 2002) discusses the taxonomic history and characteristics of the group.

Pseudoceratinidae Carter, 1885 has priority over Druinellidae Lendenfeld, 1889, based on Carter's (1885) creation of the higher taxon Pseudoceratida.

 

Diagnosis

Verongida in which the fibre skeleton, which is sparse, is dendritic, is made up of fibres with no investing bark, simply pith elements which are usually clear, but which occasionally can incorporate isolated fragments of debris. The fibres are extremely irregular, knotted in places, expanding and contracting along their length and below the surface fanning out in brushes. Pigmentation is uniform throughout the sponge, the surface is conulose and the texture rubbery, flexible in ramose forms, tending to incompressible in massive species.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Pseudoceratinidae Carter, 1885. pp. 1086-1088 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1086]

 

General References

Bergquist, P.R. 1995. Dictyoceratida, Dendroceratida and Verongida from the New Caledonia Lagoon (Porifera: Demospongiae). Memoirs of the Queensland Museum 38(1): 1-51

Bergquist, P.R. & Cook, S.D.C. 2002. Family Pseudoceratinidae Carter, 1885. pp. 1086-1088 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1.

 

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Genus Pseudoceratina Carter, 1885

 

Taxonomic Decision for Synonymy

 

Distribution

States

New South Wales, Queensland, Tasmania, Victoria, Western Australia


Extra Distribution Information

West Indian region.


IMCRA

Central Western Shelf Transition (28), Central Western Shelf Province (29), Western Bass Strait Shelf Transition (34), Bass Strait Shelf Province (35), Southeast Shelf Transition (37), Northwest Province (4), Northeast Shelf Province (40), Northeast Shelf Transition (41), Central Western Transition (5)

Distribution References

Diagnosis

Pseudoceratinidae with sparse fibre skeleton organised on a dendritic plan. Pith elements only are present in the fibres. The matrix of the sponge is extremely dense and heavily reinforced by collagen; the texture is hence firm, and often extremely hard and incompressible. The surface of the sponge is smooth, conulose or tuberculate.

 

Diagnosis References

Bergquist, P.R. & Cook, S.D.C. 2002. Family Pseudoceratinidae Carter, 1885. pp. 1086-1088 in Hooper, J.N.A. & van Soest, R.W.M. (eds). Systema Porifera: A guide to the classification of sponges. New York : Kluwer Academic/Plenum Publishers Vol. 1. [1086]

 

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Species Pseudoceratina durissima Carter, 1885

 

Taxonomic Decision for Synonymy

 

Distribution

States

Tasmania, Victoria, Western Australia


Extra Distribution Information

Port Phillip Heads, S of Warrnambool, and Howell's Point.


IMCRA

Central Western Shelf Transition (28), Central Western Shelf Province (29), Western Bass Strait Shelf Transition (34), Bass Strait Shelf Province (35), Southeast Shelf Transition (37), Northwest Province (4), Central Western Transition (5)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth 10–35 m.

 

General References

Carpay, M. 1986. The marine sponges of Tasmania. A checklist of a number of marine sponges, occurring along the Tasmanian coast. Unpublished M.Sc. thesis, Department of Bijzondere Dierkunde, Institute of Taxonomic Zoology, Amsterdam. pp. 1–77. [45]

 

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Species Pseudoceratina purpurea (Carter, 1880)

 

Taxonomic Decision for Synonymy

 

Distribution

States

Queensland, Western Australia


Extra Distribution Information

NW Shelf, Low Isles, Thalamita Flat, Mangrove Park, North-East Moat, also Cape Boileau/Red Sea, Indian Ocean, Indo-Malayan region, W and central Pacific.


IMCRA

Northeast Shelf Province (40), Northeast Shelf Transition (41)

Ecological Descriptors

Filter-feeder, marine, sessile.

Extra Ecological Information

Depth intertidal waters–50 m.

 

General References

Hooper, J.N.A., List-Armitage, S.E., Kennedy, J.A., Cook, S.D. & Valentine, C.A. 1999. Sponges of the Low Isles, Great Barrier Reef: an important scientific site, or a case of mistaken identity? Memoirs of the Queensland Museum 44: 249-262 [260] (Referred to in this article as 'Druinella' purpurea)

 

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Note: the generation of this complete preview for VERONGIIDA Bergquist, 1978 was cancelled at Pseudoceratina purpurea (Carter, 1880) owing to the initation of another complete preview for Crenavolva marmorata Fehse, 2007. Only one complete preview may be executed at a time. Previews were generated for 37 of 39 taxa.