Revision of the genus Latrunculia du Bocage, 1869 Porifera: Demospongiae: Latrunculiidae) with descriptions of new species from New Caledonia and the Northeastern Pacific (
Author
Samaai, Toufiek
Author
Gibbons, Mark J.
Author
Kelly, Michelle
text
Zootaxa
2006
2006-02-14
1127
1
1
71
https://biotaxa.org/Zootaxa/article/view/zootaxa.1127.1.1
journal article
10.11646/zootaxa.1127.1.1
11755334
5057828
E3B8BACE-1E5B-4E07-AB94-A4947F966483
Latrunculia (Biannulata) millerae
Alvarez
et al
., 2002
(Figs 6G, 7;
Tables 2
&
3
)
Latrunculia millerae
Alvarez
et al
. 2002
, PG. 168,
FIG. 8
Holotype
material.
Not examined,
NZOI
H798 (95DS610)
Additional
Paratype
material.
Not examined,
NZOI
P1267 (95DS89);
NZOI
P1268 (95DS810)
.
Other material examined.
QM
310738 (cross ref. Q66C2065L and Ts 121) labeled
Latrunculia brevis
identified by CNB,
Fiordlands
,
New Zealand
, depth
16 m
, AIMS/NCI collection
.
QM
312177 (cross ref. Q66C6062G and Ts 118) labeled
Latrunculia brevis
unidentified sponge in
QM
collection,
Fiordland
,
New Zealand
,
45º 00' 60"S
;
167º 09'40"E
, depth
30 m
, AIMS/NCI collection
.
Diagnosis
. Massive, ovosemispherical sponges with generally flattened cylindricalshaped oscules and with numerous short, thin lipped craterlike areolate porefields that are covered with a fleshy poral membrane. Colour in life green; in preservative dark brown. Styles are fusiform and slightly sinuous, occasionally hastate and polytylote, 382 (338–433) x 6 (4–8) m, n=20. Anisodiscorhabds (Fig. 6G) have an expanded manubrium. There is also no basal whorl of spines present above the manubrium as characteristic for this subgenus. The median and subsidiary whorls are deeply notched along the rim and divided into four segments, each segment possessing denticulate margins of 4–5 spines. These spines may be smooth or rough, often arrow shaped with serrated edges. The spines of the apical whorl are slanted upwards ending in a crownlike tuft of acute spined projections, 37 (32–43) x 5 (3–7) m, n=20. The choanosomal skeleton consists of a loose, irregular polygonalmeshed reticulation sometimes vaguely defined, and merging with the inner ectosomal region where the meshes become more oval and triangular (see
Fig. 8B
in
Alvarez
et al
. 2002
). Beneath the discorhabds in the ectosome is a thick paratangential layer of densely interlocking megascleres, approximately
100–300 m
deep (after
Alvarez
et al
. 2002
).
Off the
New Zealand
coastline the species are found in a calm, low light and salinity environment, typically that displayed in fiords. It is attached to vertical rock walls, and not confined to shaded areas as in the other
New Zealand
species. Depth range
5–37 m
depth.
Geographic distribution
(
Fig. 7
).
New Zealand
(South Island)
Remarks.
Miller
et al
., (2001) and Alvarez
et al
., (2002) clearly differentiated this species from
L. kaakaariki
,
L. wellingtonensis
and
L. Kaikoura
on the basis of genetic differences, morphometric differences in the acanthodiscorhabd (
Table 3
) and on morphological differences in the subectosomal region of the skeleton. This species also includes the genetic group identified by
Miller
et al
. (2001)
as “Fiordland B, separating it from
L. fiordensis
Alvarez
et al
. (2002)
. Apart from the genetic differences,
L. fiordensis
are clearly separated from
L. millerae
on the basis of the acanthodiscorhabd morphology, and are currently placed within the subgenus
Latrunculia
as appose to
Biannulata
for
L. millerae
.