Pinulasma bowiensis, Reiswig, 2018

Reiswig, Henry M., 2018, Four new species of Hexactinellida (Porifera) and a name replacement from the NE Pacific, Zootaxa 4466 (1), pp. 124-151 : 128-131

publication ID

https://doi.org/ 10.11646/zootaxa.4466.1.11

publication LSID

lsid:zoobank.org:pub:5410B0DF-67BA-4D9A-B891-3ADFAB79A8EC

DOI

https://doi.org/10.5281/zenodo.5970359

persistent identifier

https://treatment.plazi.org/id/039587B3-BE30-FFFE-FF51-FBC75C8D7B51

treatment provided by

Plazi

scientific name

Pinulasma bowiensis
status

sp. nov.

Pinulasma bowiensis n. sp.

( Figs 2 View FIGURE 2 , 3 View FIGURE 3 & 4 View FIGURE 4 , Table 2)

Material examined. Type material: Holotype: RBCM 016-00230-001, FV Pacific Viking, Set 18 ,0 8 June 2016, Bowie Seamount, 180 km W of Haida Gwaii (Queen Charlotte Islands), British Columbia, Canada, 53°21.1’N, 135°35.6’W, 476– 988 m.

Species diagnosis. Pinulasma with fistulous outgrowths of the dermal body wall that branch and anastomose. Dermalia and atrialia are microspined pentactins. Other spicules include tyloscopules, uncinates, two types of discohexasters and oxyhexasters.

Description. Body form of the holotype is not precisely known since it was broken during collection and recovered as about 60 hard but fragile fragments ranging in size from 2 to 121 mm ( Fig. 2A View FIGURE 2 ); it was most likely a large cone or plate. The atrial surface of the largest fragment is rather smooth with large evenly-spaced openings ( Fig. 2B View FIGURE 2 ), 4.7– 6.9 –9.2 (n = 15) mm in diameter and 15– 20 –25 (n = 21) mm center-to-center spacing, extending vertically outwards into diverticula of the dermal surface. On the dermal surface, those atrial apertures extend into hollow dermal processes that extend vertically outwards 2–3 cm from the dermal surface and bend rather abruptly to extend parallel to the body wall and anteriorly as evidenced by orientation of dictyonal skeleton ( Figs 2A, C– D View FIGURE 2 ).The dermal processes are somewhat flattened laterally and they often assume wall- or ridge-like form containing the round tubular component distally. The outer horizontal components of dermal processes commonly branch and anastomose; their distal walls often remain incompletely fused ( Fig. 2C View FIGURE 2 ) or, if completely fused they bear small apertures as parietal oscula along their outer surfaces and at their terminal ends ( Figs 2D–F View FIGURE 2 ), with diameters of 0.6– 2.7 –6.0 (n = 23) mm. The fragments preserved in alcohol are white.

The dictyonal framework of the fragments, and thus the entire specimen, is delicate and fragile; it consists of two components, the main wall of the specimen and walls of the dermal processes ( Figs 3A–B View FIGURE 3 ). The dictyonal framework of the main wall consists of three layers, a primary unchannelized layer with elongate meshes and nodes and short beams lined up in-register to form transverse septa or ranks ( Figs 3C–E View FIGURE 3 ). The thick dermal cortex layer of the main wall is channelized by cylindrical epirhyses ( Fig 3D View FIGURE 3 ). The atrial layer is generally too thin to show channels but its channelization cannot be ruled out with the little information provided by this single specimen. In contrast to the main wall framework, that of the dermal processes shows a distinctive difference. About one cm outwards on the dermal processes the skeleton shifts from a 3 layered form with septate middle layer to a 1-layered framework without a distinct differentiated primary layer, without septa and with meshes of fairly equal sides ( Figs 3B, F View FIGURE 3 ). Dictyonal spurs are rough and lanceolate ( Fig. 3G View FIGURE 3 ) and the framework is inconsistently ornamented with small spines, some areas being smooth ( Fig. 3H View FIGURE 3 ).

Megascleres (for measurements see Table 2) consist of a pentactine dermalia and atrialia, tyloscopules, small oxyhexactins and uncinates. Dermalia and atrialia ( Fig. 4A View FIGURE 4 ) are regular pentactins that are similar in form and size, but those of the outer surfaces are slightly larger. They are entirely and evenly covered by fine spines. Tangential ray- ends are round, proximal ray ends are bluntly pointed. The tyloscopules ( Fig. 4B View FIGURE 4 ) are likewise similar on both sides of the body wall; all encountered have 4 tines ending in spherical tips. Some have a smooth shaft, some are entirely covered by fine spines but all heads are covered by small reclined spines. Small oxyhexactins ( Fig. 4C View FIGURE 4 ) which occur loose as single spicules or grouped by fusion as small groups; they are not found attached to the framework. They are uniformly covered by strong spines and ray tips are either finely tapered to sharp tips or bluntly pointed. Uncinates ( Fig. 4D View FIGURE 4 ) are oriented obliquely throughout the wall; they are straight with welldeveloped brackets and barbs moderately inclined to the spicule surface.

Microscleres are two size classes of discohexasters, regular oxyhexasters, rare hemioxyhexasters and even rarer oxyhexactins. Oxy–tip microscleres are far more abundant (82% of 400) than disco-tip microscleres (18%). The small discohexasters 1 ( Fig. 4E View FIGURE 4 upper, F left) are somewhat stellate and have 3–11 sigmoid terminal rays originating from the sides of a small swelling at the tip of the primary ray; occasionally single terminal rays originate below the end of the primary ray. All surfaces bear small reclined spines; terminal rays end in a disc with 4–6 marginal spines. The larger discohexasters 2 ( Figs 4E View FIGURE 4 lower, F right) are more stellate with 2–4 sigmoid terminal rays originating obliquely from the tip, not sides, of each primary ray. Terminal rays are finely spined but primary rays are smooth. Oxyhexasters and rare hemioxyhexasters ( Figs 4G–H View FIGURE 4 ) have the form of discohexaster 2 in shape (main curvature of terminal rays, if present, is outwards in middle) and in the origin of terminal rays (obliquely from the end of the distal rays). They are entirely rough. Oxyhexactins are similar to oxyhexasters but slightly larger.

Etymology. The species name, bowiensis , refers to the location of collection, Bowie Seamount Marine Protected Area.

Remarks. This specimen with its three-layer dictyonal framework of the main body wall with a primary layer of elongate prismatic meshes and dermal and atrial cortices is consistent with diagnoses of the genera Chonelasma Schulze, 1886 and Pinulasma . In its fistular body wall, however, it is very similar to P. fistulosum and unlike Chonelasma , all species of which are without fistular body walls. The dictyonal framework of the Bowie specimen is nearly identical to that of the Aleutian P. fistulosum and if the only material available were the frameworks, they would probably be considered conspecific. But we have the spicules and there are major differences between them. Pinulasma fistulosum has hexactine dermalia and atrialia (vs pentactin dermalia and atrialia in the Bowie specimen), both discoscopule and strongyloscopule (vs tyloscopule) and discohexactin as the main microsclere (vs oxyhexaster). Based upon these differences, the new specimen from Bowie Seamount is considered the first member of a new species described here and named Pinulasma bowiensis .

In forming the genus Pinulasma, Reiswig & Stone (2013) considered two points of difference from Chonelasma to be of prime importance, its fistular body wall and pinular dermalia. By assigning the Bowie specimen as only the second species of Pinulasma , it is not surprising that the genus diagnosis needs to be altered; importance of the form of dermalia is now decreased and the fistular body wall has become a stronger defining character of the genus.

RBCM

Royal British Columbia Museum

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