Haliclona (Reniera) portroyalensis n. sp., a new chalinid sponge (Porifera, Demospongiae, Haplosclerida) from the southeast coast of Jamaica
Author
Jackson, Celia P. J.
Author
De, Wallie H.
Author
Weerdt
Author
Webber, Mona K.
text
Zootaxa
2006
1319
59
68
journal article
10.5281/zenodo.173994
c66089a5-c7af-4f1b-9c34-4f2500f7144b
11755326
173994
Subgenus
Reniera
Schmidt 1862
Definition
.
Chalinidae
with a choanosomal skeleton consisting of a delicate, regular, unispicular, isotropic reticulation. Ectosomal skeleton, if present, also a tangential, unispicular, isotropic, very regular and continuous reticulation. Spongin always present at the nodes of the spicules, but never abundant. Microscleres, if present, toxas and sigmas. Sponges commonly soft and fragile.
Type
species.
Reniera aquaeductus
Schmidt 1962
.
Remarks.
For synonymy and discussion of the subgenus
Reniera
see
De
Weerdt (2002)
.
Haliclona (Reniera) portroyalensis
n
.
sp.
(
Figs. 1–5
)
Holotype
:
ZMA
Por. 19096 (fragment deposited as
PRML
Por. 3905.
JAMAICA
: Port Royal
: Fort Rocky lagoon, Kingston Harbour complex,
17°56’N
76°50’W
, from prop root of red mangrove,
Rhizophora mangle
,
1.25 m
, coll. C. Jackson
1 July
, 1999 (# 39).
Description of the
holotype
(now fragmented). Shape and size (
Fig. 1
): digitate, with a few slightly swollen areas, to
6 cm
high and
1 cm
thick. Oscula scattered, some laterally flush with the surface, measuring
2–3 mm
, and one up to
6 mm
at the bulbous basis. Surface smooth and even, microhispid. Consistency. Soft, easily torn, but somewhat resilient. Colour. Purple alive, beige in alcohol.
Ectosomal skeleton (
Fig. 2
). Dermis not easily removed, pierced by pores of 55.5–88.8 µm in diameter. Pores irregularly distributed. Spongin particularly evident at the nodes, some spicules wholly enclosed in spongin.
Choanosomal skeleton (
Fig. 3
). A unispicular reticulation, but less uniform than that of the ectosome. There are also some multispicular tracts of varying length. Numerous toxas are dispersed throughout the structure of the sponge. A few collagen fibres up to 37 µm wide with no interconnections are irregularly placed within the matrix of the sponge. Spicula (
Fig. 4
): megascleres: oxeas, straight to slightly curved, with short, conical points, measuring [max
mean
(standard deviation)max] 153–177 (15.4)–209.7
x 6–7
(0.9)–8.7 µm. Microscleres: toxas, numerous in the ectosome and choanosome, very variable in length and curvature, 3.6 x ca. 0.3 µm to 112.5 x ca. 1.5 µm.
FIGURE 1.
Haliclona (Reniera) portroyalensis
n. sp.
, holotype, preserved specimen.
FIGURE 2.
Haliclona (Reniera) portroyalensis
n. sp.
, holotype, Transverse section showing skeletal structure of the choanosome. Scale bar = 100 µm.
FIGURE 3.
Haliclona (Reniera) portroyalensis
n. sp.
, holotype, Tangential view of the ectosome. Scale bar = 100 µm.
FIGURE 4.
Haliclona (Reniera) portroyalensis
n. sp.
, holotype, SEM photo of spicules. Scale bar = 100 µm.
Numerous gemmulelike bodies (
Fig. 5
) measuring an average of 55.5 µm, with thin spicules arranged in a confused manner were present in the
holotype
.
FIGURE 5.
Haliclona (Reniera) portroyalensis
n. sp.
, holotype, gemmulelike body. Scale bar = 100 µm.
Habitat and distribution
. Prop roots of the red mangrove,
Rhizophora mangle
. Known only from the
type
locality, Port Royal,
Jamaica
.
Etymology. Named after its
type
locality, Port Royal.
RemarkS
. Although none of the characters is unique, the combination of the unispicular, isotropic skeleton typical of the subgenus
Reniera
, digitate shape, conical pointed oxeas and toxas of variable length distinguishes
Haliclona (Reniera) portroyalensis
n. sp.
from other members of the genus and subgenus occurring in the Caribbean. Although only a few specimens of our new species were found at mangrove roots in Port Royal, it seems premature to conclude that the species is endemic to
Jamaica
. Systematic studies of similar habitats in other Caribbean localities are necessary to reveal its occurrence outside
Jamaica
and its distribution throughout and outside the Caribbean.
The new species cannot be confused with digitate forms of
Chalinula molitba
(
De
Laubenfels, 1949
)
(cf.
De
Weerdt 2000
, fig. 2E), a widespread Caribbean species, also known from the Azores and Canary Islands but not from
Jamaica
, because this species has the skeleton typical of the genus
Chalinula
, i.e. primary and secondary lines which are both more than one spicule long, it has oxeas which vary from vestigial strongyloxeas with truncated ends to sharply pointed oxeas, but which are never conical, no toxas, and an extremely soft and limp consistency.
Haliclona (Soestella) luciensis
De
Weerdt 2000
, only known from its
type
locality
St. Lucia
, has conical pointed oxeas of ca. 145–174 x 4.4–7 µm, very similar in shape and size to those of
Haliclona (Reniera) portroyalensis
n. sp.
, but it has the skeleton typical of the subgenus
Soestella
, i.e. the ectosome a discontinuous, unipauspicular tangential reticulation, the oxeas showing a tendency to form rounded meshes, and a choanosome with somewhat illdefined primary and secondary lines with oxeas also showing a tendency to form unipaucispicular rounded meshes. Other differences associated with
Haliclona (Reniera) portroyalensis
n.sp.
are its laterally spreading, thickly encrusting to lobatecushion shaped form, dark brown colour, the absence of toxas, and the presence of raphides as microscleres.
Toxas in a wide size range, and of similar shape as those of
Haliclona (Reniera) portroyalensis
n.sp.
occur in
Haliclona (Reniera) ruetzleri
De
Weerdt (2000)
, a species originally described from Twin Cays,
Belize
, and recently collected by C. Jackson from the mangrove roots in Port Royal.
H. (R.) ruetzleri
belongs to same subgenus as
Haliclona (Reniera) portroyalensis
n.sp.
, which means that the species are difficult to tell apart on basis of the skeletal structure alone. The following differences are, however, sufficiently evident to distinguish the two species: shape and consistency,
H. (R.) ruetzleri
consisting of clusters of anastomosing, extremely slender and soft branches and proliferations,
H. (R.) portroyalensis
n. sp.
forming digitate and slightly swollen processes of less soft, somewhat elastic consistency; size and form of the oxeas:
H. (R.) ruetzleri
having oxeas of smaller size (105–168 x 3.3–6 µm in the Twin Cays material; 102–117 x 3.6–6 µm in the Jamaican material) with long and sharp points versus the conical, short pointed oxeas of
H. (R.) portroyalensis
n. sp, in which they measure 153–210
x 6
–8.7 µm; the presence of sigmas of variable size in addition to the toxas in
H. (R.) ruetzleri
, which are absent in
H. (R.) portroyalensis
n. sp.
scarce spongin in
H. (R.) ruetzleri
versus rather abundant spongin in
H. (R.) portroyalensis
n. sp.
; and the colour which is light brown in
H. (R.) ruetzleri
and purple in
H. (R.) portroyalensis
n. sp.
The other Caribbean chalinids of the subgenus
Reniera
are:
Haliclona (R.) implexiformis
(
Hechtel 1965
)
,
H. (R.) manglaris
Alcolado 1984
,
H. (R.) mucifibrosa
De
Weerdt
et al.
1991
,
H. (R.) ruetzleri
De
Weerdt 2000
, and
H. (R.) tubifera
(
George & Wilson 1919
)
.
Haliclona (R.) implexiformis
is cushionshaped with welldefined, regular outline and large, conspicuous oxeas rounded at the ends with strongylote spicula of ca. 95–167 x 3.7–9.3 µm.
Haliclona (R.) manglaris
consists of laterally spreading sheets of conspicuous bright turquoise green colour, with sharply pointed oxeas of ca. 75–108
x 2–4
µm. It is known from several Caribbean localities, but not from
Jamaica
(
De
Weerdt, 2000
).
Haliclona (R.) mucifobrosa
consists of irregular, lumpy masses with short, truncate oscular chimneys grayish purple to bluish grey colour, with large oxeas of ca. 185–250 x 7.4–13.5 µm.
Haliclona (R.) tubifera
consists of cushionshaped masses with volcano or chimney shaped oscular elevations, frequently with numerous long, thin proliferations branching off from the main body, with oxeas of ca. 105–170
x 4
–9.5 µm.