Hymenancora cristoboi, Van, Rob W. M., 2017

Van, Rob W. M., 2017, Sponges of the Guyana Shelf, Zootaxa 1, pp. 1-225: 163-165

publication ID

http://doi.org/ 10.5281/zenodo.272951

publication LSID

lsid:zoobank.org:pub:6D68A019-6F63-4AA4-A8B3-92D351F1F69B

persistent identifier

http://treatment.plazi.org/id/03A80010-77F5-FF08-FF14-A67E94F6FCE5

treatment provided by

Plazi

scientific name

Hymenancora cristoboi
status

sp. nov.

Hymenancora cristoboi  sp. nov.

Figures 102View FIGURE 102 a –i

Material examined. Holotype RMNH Por. 9920, Suriname, ‘ Luymes O.C.P.S. II’ Guyana Shelf Expedition, station M97, 7.3083°N 54.1667°W, depth 130 m, bottom coarse sand, 16 April 1969GoogleMaps  .

Description. ( Fig. 102View FIGURE 102 a) Thinly encrusting on a piece of a dead bryozoan, surface smooth but irregular. Lateral size about 1 x 1 cm, thicknes <1 mm. Color in alcohol pale orange. Consistency soft.

Skeleton. Hymedesmioid, with larger and smaller acanthostyles erect on the substratum, and scattered tornotes and abundant microscleres in the ectosomal and subectosomal regions.

Spicules. ( Figs 102View FIGURE 102 b –i) Acanthostyles, tornotes, anchorate isochelae, sigmas.

Acanthostyles in a wide size range, divisible into larger partially spined (shaft smooth or sparingly spined) and smaller entirely spined categories, both provided with swollen profusedly spined heads; (1) large acanthostyles ( Figs 102View FIGURE 102 b,b1) 174– 214 –237 x 12 – 14.2 –18 µm, and (2) small acanthostyles ( Figs 102View FIGURE 102 c,c1), 83– 95 –106 x 7 – 8.8 –10 µm.

Tornotes ( Figs 102View FIGURE 102 d), with mucronate apices, slightly dissimilar at opposite ends, either lightly spined ( Fig. 102View FIGURE 102 d,d1) at one end, these forming a minority, or entirely smooth ( Figs 102View FIGURE 102 d2,d3), forming the majority, size 156– 177 –201 x 3 – 3.6 –5 µm.

Anchorate isochelae tridentate with incipient fimbriae at opposite ends on the shaft; there are three size categories, the larger and middle-sized chelae ( Figs 102View FIGURE 102 e –f) shaped similarly, the smallest (G= Fig. 102View FIGURE 102 g) more elongate; (1) largest chelae ( Fig. 102View FIGURE 102 e), occasionally with four alae instead of three, caused by a split in the innermost ala, 36– 49.2 –54 µm, (2) middle-sized chelae ( Fig. 102View FIGURE 102 f), 19– 22.2 –24 µm, and (3) small chelae ( Fig. 102View FIGURE 102 g) almost overlapping in size with the middle-sized chelae but recognizable by shape, 12– 13.6 –18 µm.

Sigmas, symmetrical, with incurved apices, in a large size range, but divisible in at least two size categories (the smaller possibly further divisible), (1) larger ( Fig. 102View FIGURE 102 h), 69– 81.3 –97 µm, and (2) smaller ( Fig. 102View FIGURE 102 i), 18– 41.4 –54 µm.

Distribution and ecology. Guyana Shelf, sandy bottom at 130 m depth.

Etymology. Named after Dr Javier Cristobo (Instituto Español de Oceanografia, Gijon, Spain) to acknowledge his great efforts to unravel poecilosclerid taxonomy.

Remarks. To date no Hymenancora  species have been reported from the Tropical Western Atlantic region. The genus is typically confined to colder and deeper waters. The present species appears close to the Chilean species H. tenuissima ( Thiele, 1905)  (as Hymedesmia  ). This differs from the present species in having only a single sigma category and only two chela categories the smaller of which has 5 alae, and all tornotes are heavily spined. Antarctic H. rufa ( Kirkpatrick, 1907)  (as Hymeraphia  ) is also similar but lacks sigmas entirely. The nearest record of Hymenancora  is likely from Sao Paulo State at 500 m depth off SE Brazil ( Hajdu & Lopes 2007, p. 355, as Myxilla (Ectyomyxilla)  tenuissima), later reassigned to Hymenancora  by Muricy et al. 2011, p. 164. It is possible that these records concern the present new species, but since no description of this material was presented by either Hajdu & Lopes or Muricy et al. it remains uncertain what the exact identity is. Lévi (1963) reported this same species from South Africa (as Ectyomyxilla tenuissima  ), but his description does not conform to Thiele’s, and this sponge is not likely to belong to Hymenancora  .

I take this opportunity to discuss several homonyms involving the species name tenuissima  .

Hymedesmia tenuissima Thiele, 1905  (p. 454) was transferred to Ectyomyxilla  by Lévi (1963) (but see above), to Myxilla  ( Ectyomyxilla  ) by Hajdu & Lopes (2007) and subsequently to Hymenancora  by Van Soest (2002c).

Myxilla tenuissima Dendy, 1905  (p. 169) was transferred to Hymedesmia  by Topsent (1928) (p. 252) without comment. It is quite clear from Dendy’s description and figures of the spicules, that Topsent was right in considering Myxilla tenuissima  to be a Hymedesmia  . Topsent’s use of the combination Hymedesmia tenuissima (Dendy)  created a secondary junior homonym of Thiele’s Hymedesmia tenuissima  , but since the latter is now no longer considered congeneric with Hymedesmia  , H. (H.) tenuissima ( Dendy, 1905)  remains valid.

The combination Myxilla tenuissima Row, 1911  (p. 345) is a junior primary homonym of Myxilla tenuissima Dendy, 1905  . Even though Dendy’s species is now considered a Hymedesmia  , this necessitates proposing a new name ( ICZN art. 57.2). From its description, it is very likely that Row’s species is also a Hymedesmia  , close to Dendy’s tenuissima  , but its black color (vs. Dendy’s yellow) prevents synonymy of the two. In conclusion, I here propose Hymedesmia (Hymedesmia) rowi  nom. nov. to replace Row’s Myxilla tenuissima  .

RMNH

National Museum of Natural History, Naturalis

Kingdom

Animalia

Phylum

Porifera

Class

Demospongiae

Order

Poecilosclerida

Family

Myxillidae

Genus

Hymenancora

Loc

Hymenancora cristoboi

Van, Rob W. M. 2017
2017
Loc

Myxilla tenuissima

Row 1911
1911
Loc

Hymedesmia tenuissima

Thiele 1905
1905
Loc

Myxilla tenuissima

Dendy 1905
1905
Loc

H. (H.) tenuissima (

Dendy 1905
1905
Loc

Myxilla tenuissima

Dendy 1905
1905