Amphimedon species (Porifera: Niphatidae) from the Gulf of Aqaba, Northern Red Sea: Filling the gaps in the distribution of a common pantropical genus
Author
Helmy, Tamer
Author
Van, Rob W. M.
Author
Soest
text
Zootaxa
2005
859
1
18
journal article
10.5281/zenodo.170840
c0e87963-d99a-4ac4-ab32-41d41d140df9
11755326
170840
Amphimedon chloros
Ilan et al., 2004
(
Figs 2A
–C)
Synonymy.
Dactylochalina viridis
Keller, 1889
: 391
;?
Pachychalina variabilis
;
Row, 1911
: 321 (not:Dendy, 1890);
Hemihaliclonaviridis
;
Burton,1937
: 18, pl. Ifig.7 (withadditionalsynonyms, but these appear mostly unsustained);
Callyspongia viridis
;
Burton, 1952
: 167;
Amphimedon chloro
s
Ilan et al., 2004
: 11, fig. 7.
Material examined.
ZMA
Por. 17340, Shark Observatory,
3m
, coll. T. Helmy,
2607 2000
.
Description.
Colour: Brown when dried or preserved in alcohol, presumably green in life (not recorded). Shape: Lobate, size
25 cm
x
10
cm, attached to hard substrata, with hollow upright, fingerlike projections up to
7 cm
high. Oscula are distinct,
3–5 mm
wide, and scattered over the surface (
Figure 2A
). Surface: Optically smooth, slightly bumpy surface. Punctate due to regularly distributed subdermal spaces. Texture: Compressible, soft, easy to tear.
FIGURE 2.
A.
Amphimedon chloros
Ilan et al., 2004
, habit (scale bar = 1 cm); B.
Amphimedon chloros
Ilan et al., 2004
, structure of the ectosomal skeleton showing the threedimensional network of spicule tracts (scale bar = 0.5 mm); C–F. SEMimages of oxeas of
Amphimedon chloros
(C),
A.dinae
sp.nov.
(D),
A.jalae
sp.nov.
(E) and
A.hamadai
sp.nov.
(F) (scale bars = 10 µm).
Skeleton
. Ectosomal skeleton composed of a threedimensional reticulation of uni, pauci or plurispicular spicule tracts of 10–65 µm diameter forming rounded meshes, 90 115
130 m
diameter. Spongin is scarce and forms an indistinct thin layer enveloping and connecting the spicules. Choanosomal skeleton an anisotropic arrangement of plurispicular spicule tracts 10–80µm diameter, ascending towards and protruding slightly from the surface, causing a microconulose surface (
Figure 2
B). Meshes similar in size to those of the ectosome, but more squarish in outline, up to 200 µm in diameter. Spicules: Oxeas (
Figure 2
C), curved with sharp endings, 36120142
x 1–2
µm.
Ecology.
Found on the reef flat, attached to undersides of rocks or sometimes on silt bottoms.
Distribution
. Widely distributed in the Gulf of Aqaba (pers. obs. T.H.) and frequently recorded from other areas, such as the coasts of Jeddah and Eilat.
Remarks
. We were able to verify the identity of the collected specimen with
Dactylochalina viridis
Keller, 1889
by the examination of a microscopical slide of the Berlin Museum
type
specimen ZMB 7654. The genus
Dactylochalina
Lendenfeld, 1886
to which
Keller (1889)
assigned this species is a synonym of
Callyspongia (Callyspongia)
according to
DesqueyrouxFaúndez & Valentine, 2002
, and thus
D. viridis
was wrongly assigned.
Ilan et al., 2004
made it clear that it belongs to the genus
Amphimedon
, and consequently they had to give it a new name (
A. chloros
) because the combination
Amphimedon viridis
is preoccupied by a clearly different species, the Caribbean
A. viridis
Duchassaing & Michelotti, 1864
.
Burton (1937)
made Duchassaing & Michelotti's
A. viridis
the
type
of a genus
Hemihaliclona
, which falls into synonymy with
Amphimedon
according to
DesqueyrouxFaúndez & Valentine, 2002
. Burton (l.c.) gave a large number of synonyms for
D. viridis
including the names of several Caribbean and South Australian species. We cannot here decide whether all these synonyms are proper, but grave doubts are in order in view of the implied cosmopolitan nature of such a widespread species. We did check whether the Red Sea species
Reniera tabernacula
Row, 1911
, allegedly also a synonym according to Burton, conforms to
Dactylochalina viridis
/
Amphimedon chloros
by studying slides of the
type
of
Reniera tabernacula
, BMNH 1926.2.11.18.
Reniera tabernacula
is a green, flattened and lamellar mass, with a clear
Haliclona (Reniera)
type
ladderlike skeleton unlike that of
A. chloros
, with spicules relatively robust, straight and abruptly pointed, unlike the thinner, curved oxeas of
A. chloros
.
It is likely that the material named
Pachychalina variabilis
by
Row, 1911
is also a specimen of this species, although we did not attempt to verify this. The description of the habit and the skeleton is similar to the one presented above. The original
Pachychalina variabilis
Dendy, 1887
is Caribbean (
Bahamas
) and was assigned to
Amphimedon complanata
(Duchassaing, 1850)
by Wiedenmayer (1977) and to
Cribrochalina variabilis
by
Van Soest (1980)
; in any case this is a clearly different species not to be confused with the Red Sea species.
A. chloros
is not the only green
Amphimedon
in the IndoPacific as there is also
A. paraviridis
Fromont (1993)
from North
Australia
and
Indonesia
. This is different in shape, thickly encrusting to ramose,
20 mm
in thickness with slightly raised oscules. The skeleton forms a loose reticulation with in addition many interstitial spicules between the fibres, and spicules are longer and thicker: 114–204
x 4
–10.5 µm (
Fromont, 1993
).