Rossellid glass sponges (Porifera, Hexactinellida) from New Zealand waters, with description of one new genus and six new species

Abstract New Zealand’s surrounding deep waters have become known as a diversity hotspot for glass sponges (Porifera: Hexactinellida) in recent years, and description and collection efforts are continuing. Here we report on eight rossellids (Hexasterophora: Lyssacinosida: Rossellidae) collected during the 2017 RV Sonne cruise SO254 by ROV Kiel 6000 as part of Project PoribacNewZ of the University of Oldenburg, Germany. The material includes six species new to science, two of which are assigned to a so far undescribed genus; we further re-describe two previously known species. The known extant rossellid diversity from the New Zealand region is thus almost doubled, from nine species in five genera to 17 species in eight genera. The specimens described here are only a small fraction of hexactinellids collected on cruise SO254. Unfortunately, the first author passed away while working on this collection, only being able to complete the nine descriptions reported here. The paper concludes with an obituary to him, the world-leading expert on glass sponge taxonomy who will be greatly missed.


Introduction
The deep sea of the New Zealand region has only recently been recognised as a hotspot of glass sponge diversity, with two major monographs treating the dictyonal and euplectellid hexactinellids Kelly 2011, 2018). However, the family Rossellidae Schulze, 1885(order Lyssacinosida Zittel, 1877, has not been extensively treated thus far. In a literature review of the sponge fauna of New Zealand, Dawson (1993) listed three species of rossellid glass sponges in New Zealand waters: Aulochone cylindrica Schulze, 1886 [now accepted as Crateromorpha (Aulochone) cylindrica], Rossella ijimai Dendy, 1924, andSymplectella rowi Dendy, 1924 (see also Dohrmann 2016). Symplectella rowi, and to a lesser extent, Rossella ijimai, are now fairly well known because they occur in relatively shallow water in many parts of the New Zealand Exclusive Economic Zone, and they have distinctive morphologies that are easily identifiable from images captured in situ by deep-water imaging systems.
The endemic genus Symplectella Dendy, 1924 and only known species, S. rowi, was first collected from the Terra Nova Expedition Station 96, 7 miles (11.5 km) east of North Cape on the eastern tip of the North Island, at a depth of 70 fathoms (128 m). It is now known to be relatively common around New Zealand, from the type locality south along the East Coast to the Bay of Plenty, East Cape. In the South Island, the distribution extends from southeast of Cook Strait and Kaikoura Coast out onto the Chatham Rise and deep into the subantarctic New Zealand region. Symplectella rowi is less common on the West Coast of both Islands, but this is not an unusual distribution pattern for New Zealand Porifera and may reflect the lighter collection effort on that coastline. The species is, however, quite common in Fiordland (Battershill et al. 2010), where it is found in deep SCUBA-diving depths (up to ~ 30 m), along with other attractions such as endemic black and red corals, hydrozoan sea fans, and sea pens that also occur in shallow depths and are impressive tourist attractions. Recently, several important regional populations have come to light in the North Island: off Rakitu Island, Great Barrier Island, Hauraki Gulf (Lee et al. 2015;Kelly 2016); off Mimiwhangata, Northland (Kerr and Doak, pers. comm.); and in the North Taranaki Bight (Jones et al. 2018).
Rossella ijimai was collected from the same Terra Nova Expedition station as S. rowi, ~ 12 km east of North Cape, at 128 m. It is now known from the continental shelf around Northland on both the west and east coasts, and on the Chatham Rise. Rossella ijimai and S. rowi often co-occur and so the important North Island regional populations of the more abundant S. rowi include the odd specimen of R. ijimai. Of special interest is the North Taranaki Bight population, discovered only in 2018, where the two species co-occur in relatively high numbers. Recent NIWA and Department of Conservation ROV surveys around Fiordland revealed the first, albeit unconfirmed record of R. ijimai (Page and Handley, pers. comm.).
In 2013, several well-preserved body fossils of a new species, Rossella cylindrica Buckeridge & Kelly, 2013(in Buckeridge et al. 2013, from the late Palaeocene-early Eocene Red Bluff Tuff of Chatham Island, were confirmed by HMR. Both R. antarctica Carter, 1872 andR. racovitzae Topsent, 1901 were stated to be present on the Chatham Rise, but this remains unconfirmed. Various Rossellidae species were also represented in the Oamaru Diatomite (Eocene) as hexactins, pentactins, and stauractins, illustrated in Hinde and Holmes (1892), but microfossil spicules were not recorded in the Tutuiri Greensand (Kelly and Buckeridge 2005), despite the relatively high proportion of hexactinellid taxa in the fauna. Specimens compared to Rossella racovitzae/R. antarctica on the Chatham Rise by Buckeridge et al. (2013) and Campbell Plateau (Chin and Kelly, pers. comm.) form a small, squat, open-mouthed barrel with a restricted base, and have a characteristic veil of hypodermal pentactins protruding beyond the surface of the sponge wall. This latter character is highly reminiscent of the new species described herein, Nubes tubulata gen. nov., sp. nov. and Scyphidium variospinosum sp. nov., the type localities of which are just north of Chatham Rise.
The 2017 German RV Sonne (cruise SO254) expedition to New Zealand afforded an important collection of ~ 100 new hexactinellid specimens and corresponding seafloor images, collected as part of Project PoribacNewZ of the Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky University of Oldenburg, using the GEOMAR Helmholtz Centre for Ocean Research Kiel Remotely Operated Vehicle (ROV) Kiel 6000 (Schupp et al. 2017). Preparation of a manuscript combining morphological descriptions and molecular systematics of these glass sponges was underway when we were devastated by the untimely death of Henry Reiswig in July 2020. The objective of this work is to provide the descriptions of specimens completed prior to Henry's passing. This work includes the establishment of a new endemic genus, Nubes gen. nov., with two new species; a new species of Bathydorus Schulze, 1886; redescription of Scyphidium australiense Tabachnick, Janussen & Menschenina, 2008, and description of a new species of Scyphidium Schulze, 1900; redescription of Caulophacus (Caulophacus) discohexaster Tabachnick & Lévi, 2004, and description of two new species of Caulophacus (Caulophacus) Schulze, 1886.

Sample collection
Specimens, seafloor images, and videos were collected as part of Project Porib-acNewZ of the Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky University of Oldenburg, on the new German RV Sonne (cruise SO254), using the GEOMAR Helmholtz Centre for Ocean Research Kiel ROV Kiel 6000 (Schupp et al. 2017). With the exception of NIWA 126016, which was collected in International Waters to the east of Norfolk Island and the Three Kings Ridge, all other specimens were collected from the New Zealand Exclusive Economic Zone (EEZ); collection sites and general distribution of the species are shown in Fig. 1.

Sample preparation
Subsamples were taken on board, stored in appropriate preservatives for morphological and molecular work, and shipped to the Ludwig-Maximilians-Universität (LMU) Munich. Specimens reported here, together with a much larger collection, the remainder of which will be reported on elsewhere, were first subjected to a molecular phylogenetic study (results not shown) based on a mitochondrial 16S ribosomal DNA fragment (cf. Dohrmann et al. 2008) for initial assessment of their relationships. This then allowed selection of interesting specimens for further study, some of which we describe below. Preliminary morphological identifications of these specimens were made by MD by analysing spicule content with light microscopy of temporary bleach digestions of tissue pieces. Sample preparation for formal identification and description of taxa new to science (as well as re-descriptions of known species where appropriate) were then performed by HMR using methods described in Kelly (2011, 2018).

Registration of type and general material
Primary and secondary type materials of new species and additional material are deposited in the Invertebrate Collection (NIC) at the National Institute of Water and Atmospheric Research (NIWA), Greta Point, Wellington, using the prefix NIWA -. Registration numbers are cited in the text. Taxonomic authority is restricted to Reiswig, Dohrmann & Kelly.

EEZ
Exclusive Economic Zone; GEOMAR Research Center for Marine Geosciences, Helmholtz Centre for Ocean Research Kiel, Germany;

ICBM
Institute for Chemistry and Biology of the Marine Environment, Carl von Ossietzky University of Oldenburg; LM light microscopy; NIC-NIWA Invertebrate Collection, NIWA, Wellington, New Zealand; with diactins or outwardly protruding hypodermal pentactins; prostalia basalia, when present, are outwardly protruding hypodermal pentactins which are usually specialised (anchorate). Choanosomal skeleton consists of diactins, sometimes together with less frequent hexactins. Hypodermal pentactins often present, usually they protrude from the dermal surface serving as prostalia. Hypoatrial pentactins are rarely found or absent in some taxa. Dermalia are combinations of various spicules usually pentactins; stauractins and diactins, rarely hexactins. Atrialia are usually hexactins but other holactinoidal spicules can be also found there. Microscleres are various: holactinoidal, asterous and asters; they usually have discoidal or oxyoidal terminations but sometimes floricoidal, onychoidal, or sigmoidal ones (after Tabachnick 2002).
Remarks. This subfamily is clearly not monophyletic (Dohrmann et al. 2017) and retained here for historical reasons only.
Description. Morphology of the holotype is a thick-walled funnel attached to rock substratum by a wide basal disc (Fig. 2B). Both dermal and atrial surfaces have a very dense, bushy, cover of prostal diactins (Fig. 2C, E, F). The single terminal osculum is the widest body part and the margin is abruptly sharpened; it has no marginalia (Fig. 2D).
Dimensions of the holotype are ~ 17.2 cm high and 12.8 cm wide; the measurements are only approximate as only one of the two laser points could be certainly found on the in-situ images. Wall thickness is 10.7 cm, excluding the 1-2.5 cm thick prostal cover layers on each side. Texture is soft, compressible, and resilient, neither hard nor fragile. Surfaces of both the inner and outer walls are hairy to the naked eye, and when inspected at low magnification of a dissecting microscope, both are covered with a bushy layer of prostal diactins. Colour in life is pale beige, and pale brown when preserved in ethanol.
Skeleton. Choanosomal skeleton consists of a loose network of thin choanosomal diactins amongst the thicker proximal ends of prostal diactins, and proximal rays of hypodermal pentactins. No choanosomal hexactins are present. There is no evidence of fusion between any spicules. Microscleres are scattered evenly throughout the choanosome. Ectosomal skeleton of the dermal side consists of abundant prostal diactins passing through the distal tangential parts of hypodermal pentactins and dermalia, which are mostly stauractins (62% of 126 assessed), pentactins (29%) and hexactins (10%).

Figure 2.
Bathydorus poculum sp. nov., holotype NIWA 126338, distribution, skeleton, and morphology A distribution in New Zealand waters B holotype in situ (scale bar approximate) C dermal (upper) and atrial (lower) sides of the preserved main part of the collected fragment D magnified area of the oscular margin, showing the atrial surface curving out over the dermal surface E dermal surface with dense prostal diactins F atrial surface with similarly dense prostal diactins. Image B captured by ROV Team GEOMAR, ROV Kiel 6000 onboard RV Sonne (voyage SO254), courtesy of Project PoribacNewZ, GEOMAR, and ICBM.
Spicules. Megascleres ( Fig. 3; Table 1) are prostal diactins, hypodermal pentactins, choanosomal diactins, dermalia mostly as stauractins, and atrialia mostly as hexactins. Prostal diactins (Fig. 3A) are long bow-shaped spicules, smooth except for patches of subterminal spines; the smooth tips are rounded or parabolic; the spicule centre is . Bathydorus poculum sp. nov., holotype NIWA 126338 spicules A prostal diactin, whole and enlarged end B hypodermal pentactin, whole and enlarged spicule centre, tangential and proximal ray ends C choanosomal diactin, whole and enlarged end D stauractine dermalium, whole and enlarged ray end E pinular hexactine atrialium, whole and enlarged ray end F oxyhexaster G enlarged whole primary and secondary ray (left) and centre of spicule showing smooth primary and ornamentation of spines on secondary rays (right) H hemioxyhexaster I hemioxystauraster. not swollen. Hypodermal pentactins (Fig. 3B) are regular and crucial in form with very long proximal rays, averaging 3.4 × tangential ray length, and fine spines evenly scattered over the entire surface. All five rays have subterminal patches of larger spines and smooth round tips. Choanosomal diactins (Fig. 3C) are straight, bent or more commonly sinuous in shape. Most are broken so few intact spicules are measurable for length. They are smooth except for subterminal inflated rough patches; the tip is smooth and abruptly tapered to a point. The spicule centre is moderately swollen. Dermalia ( Fig. 3D) are mainly crucial stauractins completely covered with short, rounded knobs or spines; rays are tapered to a round tip. Atrialia (Fig. 3E) are mostly hexactins ca. half of which are pinular with one ray longer than the others. Like dermalia, these are entirely covered with short, rounded knobs or spines but longer than those of the dermalia; ray tips are rounded. Microscleres ( Fig. 3; Table 1) are all oxyhexasters and their variants with hemioxyhexasters being the most common. Oxyhexasters (Fig. 3F, G) have short smooth primary rays and long straight secondary rays; the secondary rays are entirely ornamented with reclined spines that increase in size from the ray tip to its proximal end. Secondary rays on each primary ray vary from 2-5. Hemioxyhexasters (Fig. 3H) are similar to oxyhexasters but at least one of the six primary rays bear only a single secondary ray. Other rare variants include oxyhexactins, oxypentasters, and oxystaurasters (Fig. 3I). Etymology. Named for the beaker-shaped morphology of this species (poculum, beaker; Latin).
Remarks. This New Zealand specimen, NIWA 126338, is entirely consistent with the diagnosis of Bathydorus and is assigned there. Each of the known species of the genus differ from this specimen in the following characters: Bathydorus echinus Koltun, 1967 has prostal pentactins in addition to diactins, and dermalia as mainly pentactins; B. fimbriatus Schulze, 1886 has prostalia including pentactins as marginalia only, and no pinular atrialia; B. laevis laevis Schulze, 1886 has no prostalia lateralia and no pinular atrialia; B. laevis pseudospinosus Tabachnick & Menshenina, 2013 has some large choanosomal or prostal hexactins and smaller oxyhexasters to only 100 µm diameter; B. laninger Kahn, Geller, Reiswig & Smith Jr., 2013 has a flat body form and no prostalia on the atrial (upper) surface; B. servatus Topsent, 1927 has no prostal diactins, and dermalia as stauractins and diactins; B. spinosissimus Lendenfeld, 1915 has choanosomal hexactins, and oxyhexasters with longer primary rays (4-12 µm); in the original description of B. spinosus Schulze, 1886, there is no mention of hypodermal pentactins; although Tabachnick and Menshenina (2013) include these, they fail to certify that they are present in the holotype; this species also has wavy secondary rays on the oxyhexasters; B. uncifer Schulze, 1899 has smooth dermal and atrial surfaces, and dermalia as mainly pentactins and stauractins. These differences are sufficient to conclude that the new form is a new species, here designated as Bathydorus poculum sp. nov. Nubes Reiswig, Dohrmann & Kelly, gen. nov. http://zoobank.org/032AA823-2695-4E82-888D-0051A86BC438 Diagnosis. Rossellinae with basiphytous, saccular, thick-walled body, unstalked or with a short stalk. Hypodermalia are large, raised, paratropal or orthotropal pentactins with strongly curved or straight tangential rays, smooth except for rough tips, forming a cloud or veil around the thick-walled body. Prostal diactins are marginalia only. Choanosomal spicules are diactins and sometimes large hexactins with curved rays, smooth except for rough tips. Dermalia are mainly stauractins and pentactins. Atrialia are mainly hexactins and sometimes pentactins. Microscleres are oxyhexasters, hemioxyhexasters, and anisodiscohexasters.
Etymology. Named for the cloud of large hypodermal pentactins that veils the body of these sponges (nubes, cloud; Latin).
Remarks. This new genus diagnosis differs from those of most other anisodiscohexaster-bearing genera or subgenera in the following ways: from Anoxycalyx Kirkpatrick, 1907 in not having anchorate hypodermalia, and having pleural hypodermalia raised, having marginalia; in not including pappocomes and discohexasters other than anisodiscohexasters (strobiloidal discohexasters) as microscleres. It differs from that of Crateromorpha (Crateromorpha) Gray in Carter, 1872 in body form, having marginal diactins, and having main atrialia as hexactins. It differs from that of Rossella Carter, 1872 in having most atrialia as hexactins instead of stauractins, and no calycocomes. However, it does not differ from the present diagnosis of Vazella Gray, 1870(Tabachnick 2002 in any way, but below we offer a modified diagnosis of that genus to separate the two groups. Distribution. Known only from the type locality, Seamount 986 off Hawkes Bay shelf, east of North Island, New Zealand (Fig. 4A).

Nubes tubulata
Habitat. Attached to hard substratum; depth 767-783 m (Fig. 4B). Description. Morphology of the holotype and paratype a thick-walled, tubular sponge, attached to hard substratum by a narrow base (Fig. 4B). A round osculum of moderate size is terminal and opens into a deep atrial cavity. The margin is sharp and there are indications of sparse diactin marginalia in deck images, but we have been unable to verify them in the material at hand. The dermal surface has a dense covering of raised, prostal, hypodermal pentactins ( Fig. 4C, D, I) projecting up to 1 cm from the surface proper. There is indication in some of the deck images of long diactins projecting sparsely up to 6 cm from the dermal surface, especially basally, but these may be choanosomal diactins pulled out during collection; we have not found such large diactins in the material we had for examination. Dimensions of the holotype are ~ 13.3 cm high, 7.0 cm wide, and 10.8 (9.2-13.3) (n = 9) mm in body wall thickness; the osculum is 2.2 cm in diameter in situ. The paratype is 19.5 cm high, 13.4 cm wide, and body wall is 7.4 (5.5-9.3) (n = 11) mm in thickness. The osculum is 4.2 cm in diameter in situ. Texture is soft, compressible, and resilient, neither hard nor fragile. Surface of the dermal side is covered by a thick layer of projecting hypodermal pentactins (Fig. 4E). The dermal lattice is torn apart, and dermalia reside in preserved specimens as attached flakes on the hypodermalia (Fig. 4G). The atrial layer retains the atrial lattice covering smaller apertures (Fig. 4F, H); no large megascleres project into the atrium. Colour in life is transparent white, preserved in ethanol is medium brown (Fig. 4C).
Skeleton. Choanosomal skeleton consists of a loose, vacuolar network of thin choanosomal diactins, large choanosomal hexactins, and the thicker proximal rays of the hypodermal pentactins. There is no evidence of fusion between any spicules. Microscleres are scattered evenly throughout the choanosome. Ectosomal skeleton of the dermal side consists of abundant prostal pentactins supporting a delicate lattice of hexactine, pentactine, and stauractine dermalia. The atrial ectosome lacks hypoatrial pentactins but has bands of diactins that support the atrial lattice of hexactins, providing greater support than available to the dermal lattice. Microscleres are present as in the choanosome.  Table 2) are prostal hypodermal pentactins, choanosomal diactins, choanosomal hexactins, dermalia, and atrialia. Prostal hypodermal pentactins (Fig. 5A) are mostly large, raised paratropal forms (90% of 68 scored) with long, very curved tangential rays, but some regular, crucial forms occur (10%) in smaller forms especially near the margin. Tangential rays are 1.7 × the shorter, straighter proximal rays. The spicules are smooth except for the rough sharp tips. Choanosomal diactins (Fig. 5B) are straight or strongly curved, usually with undetectable central swellings; they are smooth except for the rough, slightly inflated tips. Choanosomal hexactins (Fig. 5C) are large forms with strongly curved or nearly straight, nearly equal length rays, which are otherwise similar to those of the hypodermalia. Dermalia (Fig.  5D) are entirely spined and consist of stauractins (31% of 387 scored) and similar forms with reduced fifth ray (subpentactins) or both fifth and sixth rays in one axis (subhexactins) (64%) with a few (1-2%) as tauactins, diactins and paratetractins. It Figure 5. Nubes tubulata gen. nov., sp. nov., holotype NIWA 126159, spicules A whole prostal hypodermal pentactin and enlarged ray ends B whole curved and straight choanosomal diactins with two enlarged ends; scales of whole spicules and parts in B and C as in A; C whole choanosomal hexactin with two enlarged ray ends D two dermalia, a subhexactin, and a stauractin, with enlarged ray ends and centres E two atrialia, a pinular subhexactin, and a regular hexactin with enlarged centrum of the pinular subhexactin and a ray end; scales of whole spicules and parts as in D; F two oxyhexasters G enlarged terminal ray of an oxyhexaster H anisodiscohexasters, from SEM preparation (above) and LM preparation (below).
was not possible to differentiate the subpentactins and subhexactins either wet in dishes or mounted spicule microscope slides. Tips are either rounded or more often sharp. Atrialia (Fig. 5E) are entirely spined and mostly subhexactins (71% of 125 scored) with one ray reduced or hexactins (26%) with all rays of nearly equal length; a few (1-2%) are stauractins and tauactins. Ray tips are sharp-pointed. Microscleres ( Fig. 5; Table 2) are oxyhexasters and their variants, with hemioxyhexasters being the most common, and anisodiscohexasters. Oxyhexasters and hemioxyhexasters ( Fig. 5F, G) have very short smooth primary rays and long straight secondary rays entirely ornamented with small, reclined spines. Secondary rays on each primary ray vary from 1-4. Anisodiscohexasters (Fig. 5H) are spherical with stellate discs with 4-6 marginal claws on the ends of terminal rays. Primary rays are smooth and end in strobiloid discs with a short central projecting knob. Each primary strobilum supports 30-40 terminal rays with undulating, probably helically coiled, finely rough shafts of unequal lengths. Terminal discs vary in diameter with shaft length, the longer shafts carrying the larger discs, e.g., a series 1.7, 2.5, 3.1, 3.4, 3.6, 5.4, 6.9 µm diameter for shafts 15.0, 20.5, 23.5, 27.3, 32.0. 33.4, 37.1 µm in length. These spicules look very different in LM (lower image) and SEM (upper image) due to collapse of the rays during drying for SEM and support of them by balsam in LM. Etymology. Named for the tubular morphology of the sponge (tubulata, tubular; Latin).
Remarks. The characters of these two New Zealand specimens are inconsistent with the present diagnoses of all Rossellinae genera except Vitrollula Ijima, 1898. They differ, however, from those of V. fertilis Ijima, 1898, the only species in the genus, in characters not used as diagnostic. These are that V. fertilis has a smooth surface without raised hypodermalia, but the two new specimens have a bristly surface with raised hypodermalia, and that the discohexasters of V. fertilis are isodiscohexasters while those of the new species are anisodiscohexasters. In view of these differences, we opt not to include the new species in Vitrollula nor to change the diagnosis of that genus at this time. We choose to erect a new genus in Rossellinae with characters of this and the following second species described below, and designate this species as Nubes tubulata gen. nov., sp. nov. Habitat. Attached to hard substratum; depth 1285 m (Fig. 6B). Description. Morphology of the holotype body is a thick-walled tubular sponge, attached to hard substratum, by a moderately long, narrow stalk ( Fig. 6B, C). A moderately sized, round osculum is terminal and opens into a deep atrial cavity. The margin is blunt, bordered by a band of diactine marginalia (Fig. 6D, F). The dermal surface has a dense covering of raised, prostal, hypodermal pentactins ( Fig. 6D, E), projecting up to 7 mm from the surface proper. Some of the deck images indicate long diactins projecting sparsely, up to 14 mm, from the dermal surface, but these may be foreign in origin; we have not found such large diactins in the material available for examination. Dimensions of the holotype are ~ 6 cm in total length, including the stalk of 1.8 cm length (Fig. 6G), and 3.5 cm in width; the maximum body wall thickness is 13.9 mm. The osculum is 12.3 by 16.9 mm diameter in situ. Texture is soft, compressible, and resilient, neither hard nor fragile. Surface of the dermal side below the layer of projecting hypodermal pentactins is supported by an intact tight lattice of dermalia (Fig. 6H). The atrial surface (Fig. 6I), in contrast, is torn apart by removal from supporting fluids and the atrial lattice remains only as dismembered patches attached to underlying diactins. Colour in life is pale brown as is the specimen preserved in ethanol.

Nubes poculiformis
Skeleton. Choanosomal skeleton consists of a loose, vacuolar network of thin choanosomal diactins, large choanosomal hexactins and the thicker proximal rays of the hy- podermal pentactins. There is no evidence of fusion between any spicules. Microscleres are scattered evenly throughout the choanosome. Ectosomal skeleton of the dermal side consists of abundant prostal pentactins providing good support for the sturdy lattice of stauractine (60.0% of 315 assessed), pentactine (38.4%), and rare hexactine (1.64%) dermalia. The atrial ectosome lacks hypoatrial pentactins but has bands of diactins that provide poor support for the atrial lattice of mainly hexactins (86.4% of 118 assessed), pentactins (7.5%), and stauractins (5.1%). Microscleres are present as in the choanosome. . Nubes poculiformis gen. nov., sp. nov., holotype NIWA 126016, spicules A three prostal hypodermal pentactins, the lower one in plane of tangential rays, with enlarged ray ends B whole marginal diactins (ray ends unavailable) C two whole choanosomal hexactins with two enlarged ray ends and one centrum. Scale of whole spicules as in C; D four whole stalk diactins and enlarged end E dermalia, stauractin and pentactin with enlarged ray ends F atrialium and enlarged ray end G two oxyhexasters and enlarged terminal ray H whole anisodiscohexaster; an enlarged section showing disc diameter increasing in longer terminal rays; an enlarged side view of a terminal ray and end views of terminal ray discs.
Spicules. Megascleres ( Fig. 7; Table 3) are prostal hypodermal pentactins, marginal diactins, choanosomal diactins of the body, choanosomal diactins of the stalk, dermalia and atrialia. Prostal hypodermal pentactins (Fig. 7A) are large, raised orthotropal forms with long straight tangential rays. Tangential rays are ca. one half the length of the longer straight proximal rays. The spicules are smooth except for the rough sharp or round tips. Marginalia (Fig. 7B) are long, slightly curved diactins; no intact tips were found in SEM surveys but an exhaustive survey with LM indicates tips taper to nearly invisible thinness and are quite distinct from the thick roughened tips of choanosomal diactins. Choanosomal diactins (Fig. 7C) are straight or slightly curved with undetectable central swellings; they are smooth except for the rough, slightly inflated tips. Stalk diactins (Fig. 7D) are longer and thicker than the choanosomal diactins, but otherwise similar. Dermalia (Fig. 7E) are mainly entirely rough stauractins and pentactins with rounded ray tips. Atrialia (Fig. 7F) are entirely rough hexactins with equal length rays and more acute ray tips. Microscleres ( Fig. 7; Table 3) are oxyhexasters, hemioxyhexasters, and anisodiscohexasters. Oxyhexasters (Fig. 7G) and hemioxyhexasters have very short, sparsely spined or smooth, thick primary rays, ending in swollen hemispheres; 1-7, usually 3-4, rough, straight, terminal rays tapering to pointed tips emanate from the margins and occasionally from the centre of the hemisphere. Short to very short spur-like terminal rays are common. Anisodiscohexasters (Fig. 7H) have smooth primary rays ending in ovoid strobila. Each strobilum supports ca. 20-30 rough, curved terminal rays that end in discs with 4-7 marginal discs. The tuft of terminal rays from each primary ray varies in length of rays, and with ray length the diameter of terminal discs, in a pattern that is not yet clear, but the whole spicule resembles a radially symmetrical starburst.
Etymology. Named for the goblet shape of the sponge (poculiformis, gobletshaped; Latin).
Remarks. This species differs from Nubes tubulata sp. nov. in having a short stalk and orthotropal hypodermal pentactins, but is otherwise similar enough to include it in the genus Nubes as its second species, Nubes poculiformis sp. nov.
Remarks. This modified diagnosis allows separation of the present genus, Nubes gen. nov., from Vazella on the basis of lack of thorned hypodermalia and presence of discoid microscleres that are not anisodiscohexasters in the former. Furthermore, molecular phylogenetic results do not support a close relationship of the two genera (MD, unpubl. results).

Scyphidium Schulze, 1900
Diagnosis. Body is saccular, basiphytous, sometimes rhizophytous. Choanosomal skeleton is composed of diactins. Hypodermal spicules, if present, are pentactins. Prostalia, if present, are hypodermal pentactins and/or diactins. Dermalia are stauractins and/or pentactins in various combinations. Atrialia are mainly hexactins. Microscleres are discohexasters and oxyhexasters often with hemioxyhexasters and oxyhexactins; with two or three types of discohexasters, none as calycocomes. Among the larger is a spherical form with a restricted number of secondary rays (emended from Tabachnick 2002 8A).
Habitat. Attached to hard substratum; depth 409-853 m. Description. Body form is a heavy-looking, thick-walled, club-shaped, pendant sponge with a narrow basal attachment, widening gradually to a hemispherical rounded terminal end (Fig. 8B, C) where a large osculum is centrally located. The osculum opens into a deep atrial cavity (Fig. 8D). The margin is sharp-edged with indication of sparse marginalia that do not differ from prostal diactins of the lower body. The external surface of the upper body is fairly smooth, without prostalia, but the lower half is conspicuously conulose with long prostal diactins projecting in small groups from conules (Fig. 8E). We did not have access to the basal attachment so we cannot comment on the basidictyonalia. Dimensions of the specimen are 27.6 cm in height, 11.7 cm in maximum width, 5.7-10.9 cm in diameters of the osculum, 10.0 mm in maximum wall thickness, 8.3 mm in length of projecting part of prostal diactins. Texture is firm but compressible and resilient, neither soft nor fragile. Surface of the dermal side is covered by an intact lattice of dermalia (Fig. 8G) consisting mostly of pentactins (98% of 302 assayed), and a few stauractins and diactins (1% each). The upper body surface is fairly smooth, but the lower body is covered with conspicuous conules up to 3.2 mm high, from which prostal diactins project in small groups of one to four. One large pentactin was found but it was broken and assumed to be foreign. The atrial surface is covered by a felt-like layer of disarranged atrialia (Fig. 8H) composed of hexactins (57% of 168 assayed), pentactins (20%), paratetractins (8%), diactins (6%), stauractins (5%), and triactins (3%). Colour in life is very pale brown, preserved in ethanol is medium brown. Skeleton. Choanosomal skeleton consists of a tight series of macroscopic partitions of inhalant and exhalant channels running perpendicular to the body surfaces (Fig. 8F). They consist of networks of choanosomal diactins and microscleres and in the lower body the proximal ends of the prostal diactins. A few small patches of fused choanosomal diactins occur but these are too rare to provide significant support to the body. Ectosomal skeleton of the dermal side consists of the robust lattice of Figure 9. Scyphidium australiense Tabachnick, Janussen & Menschenina, 2008, NIWA 126237, spicules A prostal diactin, whole and enlarged ends, one broken distal end and two intact proximal ends B choanosomal diactins, whole long and short versions at different scales plus enlarged tips and central swellings C dermalium: pentactin, whole and enlarged tips D atrialia, hexactin, whole and enlarged tip, pentactin, whole with enlarged tips, and paratetractin, whole; scales are the same as those for dermalium E spheres as small group of whole ones and one enlarged F discohexaster 1, whole and enlarged terminal ray end G discohexaster 2, whole and enlarged part of one ray tuft H oxyhexaster, whole and enlarged terminal ray end. Scales are the same for all whole microscleres and their enlarged parts. pentactine dermalia and in the lower body the projecting prostal diactins. The atrial ectosomal skeleton consists of the felt-like lattice of atrialia and the supporting layer of hypoatrial diactins.
Spicules. Megascleres ( Fig. 9; Table 4) are prostal diactins, choanosomal diactins, dermalia, and atrialia. Prostal diactins (Fig. 9A) are large, curved, and smooth spicules with rounded proximal tips either smooth or bearing very low suggestions of obsolete spines. They have neither an axial cross nor central swellings. Distal tips are invariably broken off. Choanosomal diactins (Fig. 9B) come in three distinct forms. The larger ones over 2 mm long are straight or slightly curved or sinuous and are smooth except for the patches of spines at the rounded or abruptly pointed tips. Those between 1 and 2 mm long have sharp tips and longer spines on the tip patches. The shortest, less than 1 mm long, are entirely spined with sharp tips and often with a central tyle or four knobs. Dermalia (Fig. 9C) are thick stubby pentactins, entirely profusely spined without a knob of a sixth ray. Atralia (Fig. 9D) are highly diverse; the most common hexactins have thinner and less densely spined rays than the dermalia. Pentactin atrialia are very similar to the dermal pentactins but have a knob in place of the sixth ray. Paratropal atrialia have rays similar to the hexactine atrialia. Spheres (Fig. 9E) are common and here considered megascleres. Microscleres ( Fig. 9; Table 4) are two types of discohexasters and one type of oxyhexaster and its variants, rare hemioxyhexasters and oxyhexactins. Discohexasters 1 (Fig. 9F) are spherical with very short smooth primary rays, each supporting 3.5 (2-5) thick secondary rays ornamented with reclined spines. Terminal discs invariably have six stout marginal teeth. Discohexasters 2 (Fig. 9G) are smaller spherical forms with each smooth primary ray supporting 6.3 (5-8) thinner terminal rays; the terminal discs also invariably have 6 marginal teeth. Oxyhexasters (Fig. 9H) are stout spherical forms with each short smooth primary ray supporting 3.2 (3-5) fully developed secondary rays ornamented with dense reclined spines and ending in sharp tips. Each oxyhexaster also has 2-12 poorly developed secondary rays only a few micrometres in length. Only one hemioxyhexaster and three oxyhexactins, all of a similar size and ray characters as the oxyhexaster, were discovered in microsclere surveys.
Remarks. The characters of this new specimen agree with those in the original description of S. australiense by Tabachnick et al. (2008) except for the absence of prostal diactins and sphere megascleres in the latter, and absence of the rare discohexactins in the former. Absence of prostal diactins in the holotype is likely attributable to it being a distal fragment where we also found no prostalia in the new specimen. Spheres appear to be spicules of erratic occurrence in hexactinellids and are unlikely to be of phylogenetic significance. Absence of discohexactins in the new specimen is not considered an important difference. Sizes and shapes of the common microscleres are similar enough in both specimens to conclude that they are from specimens of the same species. It is somewhat surprising that the authors of this species assigned it to the genus Scyphidium without altering the generic diagnosis to encompass it; we have done so here.
Prior to the discovery of a second specimen of S. australiense here, there was considerable doubt as to the true type locality of the holotype described by Tabachnick et al. (2008). This work focused on hexactinellid sponges "sampled mainly off the Australian West Coast", and the holotype was named "after the type locality of this species", i.e., Australia. However, the latitude and longitude for RV Soela Stn SO 17-80 (43°33.10'-33.05'S, 179°27.25'-27.08'E) placed the type locality as on the north central Chatham Rise on the east coast of New Zealand. The Western Australian Museum (WAM) has confirmed that the RV Soela carried out fieldwork off western and northern Australia, and that the material covered in Tabachnick et al. (2008) was sent to the MNHN to be worked on taxonomically. Unfortunately, WAM has no details for "RV Soela Stn SO 17-80" (Jane Fromont, Western Australian Museum, pers. comm.), but interestingly, the specimen reported here, NIWA 126237, is also from Chatham Rise (Pegasus Canyon Slope, off Christchurch Shelf ), intensifying the mystery surrounding the type locality of this species. Investigation of pre-2004 electronic records at NIC revealed that the specimen listed from station "RV Soela Stn SO 17-80", given in Tabachnick et al. (2008), was more likely to have been collected on the RV Sonne Cruise SO-17 on the Chatham Rise phosphorite deposits east of New Zealand (Von Rad 1984), because the NZOI Stn Z3951B from that cruise, a large grab with Porifera listed in the Remarks col-umn, has identical coordinates and similar station numbers. We are still unsure as to how the specimen reached Tabachnick's attention at the MNHN, and indeed, the whereabouts of the holotype, but we know that errors were made in translation of the station data from the specimen labels to this publication, and it is possible that Figure 10. Scyphidium variospinosum sp. nov.: A distribution in New Zealand waters, location of both holotype NIWA 126279 and paratype NIWA 126274 on Wairarapa Slope B holotype NIWA 126279 in situ (green laser spots are 6.24 cm apart) C holotype, deck image, torn open on the left side. Note the distinct pentactin veil around body D holotype, superior end, deck image, where torn wall is obvious, and osculum is partly intact on the upper left side. Scale bar unavailable E paratype, NIWA 126274 (deck images by PJS) F close view of the prostal pentactins forming the veil of the holotype G Closer view of the thorns on the prostal pentactin tangential rays H dermal surface of preserved holotype with partly damaged lattice of dermalia I atrial surface of the preserved holotype with no lattice evident. Image B captured by ROV Team GEOMAR, ROV Kiel 6000 onboard RV Sonne (voyage SO254), courtesy of Project PoribacNewZ, GEOMAR, and ICBM. the authors assumed that the RV Sonne representation of "Stn SO17/80" was just another RV Soela Stn, represented as SO 17-80 in the publication. The MNHN was temporarily closed for most of 2020 and the early months of 2021 due to measures of the French government to prevent the spread of COVID-19 (novel coronavirus disease), so the repatriation of this specimen was not able to be completed at time of publication. Figure 11. Scyphidium variospinosum sp. nov., holotype NIWA 126279, spicules A prostal diactins, two whole and enlarged end and near-end segment B prostal pentactins, two whole spicules, inside and end views and parts including a tangential ray end (top), a thorned part and a proximal end (lower). Scale bars of whole and parts are same as in A C choanosomal diactins, three whole long and short versions plus enlarged tips D one pentactine dermalium and enlarged tangential and proximal ray tips E one hexactine atrialium and enlarged ray end F discohexaster 1 and enlarged terminal ray end G discohexaster 2 with enlarged terminal ray end H discohexaster 3 I hemioxyhexaster with enlarged terminal ray end. All microscleres and their enlarged parts are at same scale bars. Distribution. Known only from two locations on the Wairarapa Slope, New Zealand (Fig. 10A). Habitat. Attached to hard substratum; depth 1631-1675 m (Fig. 10B). Description. Morphology of the holotype and paratype is a thick-walled, clubshaped sponge with a narrow basal attachment, widening gradually to a hemispherical rounded terminal end where a large osculum is centrally located (Fig. 10B-E). The osculum opens into a deep atrial cavity. The margin is sharp-edged with indication of sparse marginalia that do not differ from prostal diactins of the general body wall. The external surface of the entire body is clean and conulose, with prostal diactins and hypodermal pentactins emanating from conules in small groups of 1-10. Dimensions of the holotype and paratype are, respectively, length 16.5 and 15.8 cm, width 9.5 and, excluding the lateral bulge, 9.5 cm, diameter of the osculum 6.4 and 6.6 cm, wall thickness 11.1 and 10.0 mm. Texture is soft, compressible, and resilient, but not fragile. Surface of the dermal side is conulose and bears a layer of prostal diactins projecting 12.5 (6.5-19.3) (n = 9) mm above the dermal surface, intermingled with a veil of prostal, hypodermal, thorned, paratropal pentactins (Fig. 10F, G) projecting 8.6 (7.2-10.0) (n = 9) mm above the surface. On the surface below is a lattice of overlapping dermalia of mostly pentactins (94% and 82% of 160 and 101 assessed) (Fig. 10H). The atrial surface bears a poorly preserved atrial lattice of mostly hexactins (94.7% and 94% of 133 and 131 assessed) (Fig. 10I) forming a cover over the exhalant apertures. Colour in life and preserved is very pale brown.

Scyphidium variospinosum
Skeleton. Choanosomal skeleton is composed of choanosomal diactins without detectable macroscopic or microscopic organisation. No evidence of spicule fusion was noted in either specimen. Microscleres are scattered throughout the choanosome. Ectosomal skeleton of the dermal side consists of the prostal diactins and projecting veil of thorned pentactins. The dermal surface is covered by a robust lattice of mostly pentactine dermalia. The atrial ectosome consists of the felt-like disorganised lattice of mostly hexactine atrialia and the supporting layer of hypoatrial diactins.
Spicules. Megascleres ( Fig. 11; Table 5) are prostal diactins, prostal hypodermal pentactins, choanosomal diactins, dermalia, and atrialia. Prostal diactins (Fig. 11A) are large, curved, and smooth spicules with rough subterminal patches and round tips. They have neither axial crosses nor central swellings. Prostal hypodermal pentactins (Fig. 11B) are large spicules with proximal rays ~ 1.4 times the length of tangential rays; the tangential rays are mainly paratropal, occasionally orthotropal. Both tangential and proximal rays have smooth rounded tips, but only tangential rays bear large thorns on the middle halves of the rays. Choanosomal diactins (Fig. 11C) occur in two distinct forms. Large ones > 2 mm in length are straight, slightly curved or sinuous, and are smooth except for rough subterminal areas; tips are rounded or abruptly pointed. Small forms < 2 mm in length are entirely spined, have sharp tips and often four central knobs or a single tyle. Dermalia (Fig. 11D) are thick stubby pentactins, entirely and profusely spined without a knob of a sixth ray. Atralia (Fig. 11D) are most commonly hexactins, with rays longer, thinner, and less profusely spined than those of dermalia. Microscleres ( Fig. 11; Table 5) are three types of discohexasters and two types of oxyhexasters and their variants, rare hemioxyhexasters and oxyhexactins. The centrum in all categories tends to be varyingly swollen to the extent that the spicules approach asteroid forms. The oxyhexasters are extremely difficult to separate into types due to presence of intermediates. Discohexasters 1 (Fig. 11F) are semi-stellate with very short smooth primary rays, each supporting 4-8 gently curved secondary rays ornamented with reclined spines; terminal discs invariably have eight stout marginal teeth. Discohexasters 2 (Fig. 11G) are very slightly smaller spherical forms with each smooth primary ray supporting 2-4 straight thick terminal rays ornamented with reclined spines; the terminal discs have 5-9 marginal teeth. Discohexasters 3 (Fig. 11H) are small semi-stellate forms like discohexasters 1, with very short, smooth primary rays, each supporting 7-11 thin, curved, rough secondary rays, each ending in a terminal disc with 4-9 marginal teeth. Oxyhexasters 1, including hemioxyhexasters (Fig. 11H), are stout spherical forms with each short smooth primary ray supporting 1-3 secondary rays ornamented with dense reclined spines and ending in sharp tips. Oxyhexasters 2 (no SEM image available) are forms with very thin secondary rays and often broken; they have diverse characters but are not considered immature forms of oxyhexasters 1. The centres are very small or swollen to globular form and the distal ends of the primary rays are either very thin or globular, each primary end supports two or three thin secondary rays that appear totally smooth. We are not confident in recognising this as a spicule category since the only practical character in defining it is the thinness of the secondary rays and size. Oxyhexactins (no SEM available) are rare: only four have been verified in spicule surveys. They have characteristics of oxyhexasters 1 in the stoutness and ornamentation of their rays.
Etymology. Named for the large, irregularly thorned hypodermal pentactins, that project from the body of this species (variospinosum, with irregular thorns; Latin).
Remarks. The characters of these new specimens agree with the revised diagnosis of Scyphidium (see above) but differ from those of all eight recognised species of that genus. None has raised, thorned, hypodermal pentactins as prostalia. Only three species, S. tuberculatum (Okada, 1932), S. jamatai Tabachnick, 1991, andS. australiense Tabachnick, Janussen &Menschenina, 2008 (see above) have dermalia as mostly pentactins and atrialia as mostly hexactins, in agreement with the two new specimens. The sizes of the discohexasters are considerably smaller in all three than those in the new forms described here. On the basis of these and other differences, we are confident that the two new specimens described here represent a new species, here designated as Scyphidium variospinosum sp. nov.

Caulophacus (Caulophacus) Schulze, 1886
Diagnosis. Body is mushroom-shaped or cup-like, basiphytous with long stalk. Choanosomal spicules are diactins and hexactins. Dermalia and atrialia are pinular hexactins and/or pinular pentactins. Hypodermalia and hypoatrialia are pentactins. Microscleres are represented chiefly by spicules with discoidal terminations. They usually can be divided into two categories. The first are spicules with thick rays covered with dense spines: usually discohexactins but also discohexasters, hemidiscohexasters, and rarely discasters. The second are discohexasters with thin, smooth, or rough secondary rays usually in the form of lophodiscohexasters but sometimes calycocomes and spherical discohexasters are present among them (emended from Tabachnick 2002 Habitat. Attached to hard substratum; depth 720 to 1348 m (New Zealand locations, Fig. 12A).
Description. This description refers to New Zealand specimens only. Body forms a solitary mushroom cap-shaped upper body on a long, kinked, somewhat crooked, flattened, hollow stalk (Fig. 12B, E). Surfaces of the upper body are smooth (Fig. 12C, D) with a slight blunt eminence on the outer atrial face opposite the stalk insertion, but there is no indication of an osculum. The upper dermal surface lacks any visual indication of a lattice. The lower dermal surface of the specimen is divided by ridges into six depressions not seen in the smaller specimen. The stalks of both are flattened and that of the smaller bears a cylindrical central canal (Fig. 12F). SEM views of the  Tabachnick & Lévi, 2004, NIWA 126342, 126343, distribution, skeleton, and morphology A distribution in New Zealand waters B smaller specimen, NIWA 126342 in situ C smaller specimen atrial surface on-deck image D smaller specimen dermal surface and stalk connection (deck images by PJS) E larger specimen, NIWA 126343 in situ F section of the stalk of the smaller specimen G-I SEM images of surfaces of smaller specimen; dermal G atrial H and stalk I at same magnification. Images B and E captured by ROV Team GEOMAR, ROV Kiel 6000 onboard RV Sonne (voyage SO254), courtesy of Project PoribacNewZ, GEOMAR and ICBM. dried surfaces show pores in the dermal body surface membrane (Fig. 12G), apparently contracted pores in the atrial body surface involving the atrial pinules (Fig. 12H), and no indication of pores on the dermal stalk surface (Fig. 12I). Dimensions of the smaller specimen upper body is ~ 12.5 × 10.6 cm in diameter; stalk is 15.9 × 9.0 mm in diameter and stalk canal is 4.1 × 3.3 mm in diameter. Length of the stalk could not be approximated. The larger specimen upper body is 25.0 × 15.9 cm in diameter while the flattened stalk is 5.9 cm wide. Measurable ostia of the smaller specimen Figure 13. Caulophacus (Caulophacus) discohexaster Tabachnick & Lévi, 2004, NIWA 126342, spicules: A hypodermal body pentactin; whole and enlarged tangential and proximal ray ends B hypoatrial body pentactin; whole and enlarged tangential and proximal ray ends C hypodermal stalk pentactin; whole and enlarged tangential and proximal ray ends D choanosomal hexactins; two whole and enlarged ray end E choanosomal diactins; two whole and four enlarged ends and one central swelling F dermal body pinular hexactin G atrial body pinular hexactin H stalk dermal pinular hexactin I discohexactin J hemidiscohexaster K discohexaster and magnified terminal ray and terminal disc. Scale bars in A apply to B and C; scale bar is the same for F-H, I-K.    12G) are 70 and 99 µm in diameter. Texture of the body is firm but compressible; the stalk is hard. Surface of all parts are smooth, consisting of tight palisades of pinular rays of dermalia and atralia supported on hypodermal and hypoatrial pentactins. There are no projecting prostalia. Colour in life is pale pinkish brown as are the specimens preserved in ethanol. Skeleton. Choanosomal skeleton of the body consists of a tight network of choanosomal hexactins and diactins. There is no evidence of fusion between any spicules within the body. Microscleres are scattered evenly throughout the choanosome. The stalk internal skeleton is composed of large diactins oriented longitudinally and fused by synapticula. Ectosomal skeleton of the dermal and atrial sides consists of tightly packed pinular hexactins and very few pinular pentactins (1.6% of 623 assessed). These are supported on, respectively, hypodermal and hypoatrial pentactins which are never raised above the surfaces. Microscleres are present as in the choanosome.
Spicules. Megascleres ( Fig. 13; Table 6) are hypodermal pentactins, choanosomal hexactins and diactins, and pinular hexactins and a few pentactins. Hypodermal pentactins of the body (Fig. 13A) are regular and usually smooth except for spined ray ends; 8% have indistinct spines on the proximal part of the proximal ray. The proximal rays are longer, averaging 1.24 × the length of tangential rays. Hypoatrial pentactins of the body (Fig. 13B) are regular and spined on both ray-ends and 61% of them on the proximal part of the proximal rays. The proximal ray is longer, averaging 1.62 × the length of tangential rays. Hypodermal pentactins of the stalk (Fig. 13C) are regular in shape but significantly smaller than those of the body; they are spined only on ray ends. Tangential and proximal rays are approximately equal in length. Choanosomal hexactins (Fig. 13D) are restricted to the body; rays are smooth, and spines are restricted to the ray ends except where the ray is exceptionally short. These hexactins occur in two forms, one with a short spiny ray (upper figure) and the other with all rays approximately equal in length (lower figure). Choanosomal diactins (Fig.  13E) are straight or slightly curved and are smooth except for ends on which they have small but detectable central swellings. Dermal pinular hexactins of the body (Fig. 13F) have bushy, nearly cylindrical pinular rays with a short, thick, rounded apical tip. Tangential and proximal rays are entirely spined and approximately similar in size and shape. Very rarely, these and pinules of other body surfaces are pentactine with only a round nub in place of the proximal ray. Atrial pinular hexactins of the body (Fig. 13G) have pinular rays that taper in length of scales at both ray ends, resulting in fusiform shape. The pinular ray has a thick and rounded tip. Tangential and proximal rays are entirely spined and similar in size and shape. Stalk pinular hexactins (Fig. 12H) have a pinular ray that is squat and slightly wider than those of the body spicules. Scale lengths taper basally and apically and again the apex of the pinule is a blunt, thick cap. Tangential and proximal rays are entirely spined and similar in size and shape.
Remarks. The morphological characters of the two New Zealand specimens place them clearly in subgenus Caulophacus (Caulophacus), of which there are 22 recognised species. Table 7 compares the key morphological characters that differentiate them from each other and from the New Zealand specimens, NIWA 126342 and NIWA 126343. We admit that some of these differences are subjective and the list is not exhaustive. Table 7 shows only a single species, C. (C.) discohexaster, that has a single morphological difference from the specimens described here, i.e., the visual impression of the dermal pinule (Tabachnick and Lévi 2004: 51, fig. 24A). Measurement of the Figure 15. Caulophacus (Caulophacus) serpens sp. nov., NIWA 126084, spicules A hypodermal body pentactin B hypoatrial body pentactin C hypodermal stalk pentactin D two whole choanosomal hexactins and an enlarged ray end E two whole choanosomal diactins and enlarged ends and central swellings; F dermal body pinular pentactin G atrial body pinular pentactin H stalk dermal pinular pentactin I discohexactin with enlarged terminal ray and facial view of end disc J large thick-rayed discohexaster with two smaller thin-rayed discohexasters entangled K thin-rayed discohexaster and magnified terminal ray. Scale bar in A applies to B-E scale bar in F applies to G and H whole microscleres are at the same scale.
dermal pinule in that figure shows that the figured pinular ray is too wide (84 µm) to fit within the data given for the pinular ray of the dermal hexactin given there (106-220 µm/30-46 µm). Removing this illustration error from the list results in no differences between the New Zealand specimens and the type material described by Tabachnick and Lévi (2004) from New Caledonia; therefore, we assign the specimens to that species.  (Fig. 14A).
Habitat. Attached to large pieces of rubble lying on a sediment plain at 4816 m. Description. Morphology of the holotype a rhizome-like, hard, hollow, thin stem that creeps across the sediment seabed, attaching to rubble here and there, in places forming a tangled mass, from which arises the main mushroom-shaped body on a zigzag stem (Fig. 14B, C), and two tiny, mushroom-shaped bodies (Fig. 14D). Overall dimension of the holotype, spreading across the seabed, is 64 cm. Dimension of the larger body (Fig. 14B) is 22.2 mm in diameter and 11.2 mm in height; its associated stalk is 3.6 (2-6-4.3) (n = 12) mm in diameter. The associated stalk measures 3.3 (2.7-4.0) (n = 29) mm in diameter, the length, measured in conformation from the body to the stalk tangle, is 167 mm. The smaller bodies (Fig. 14D) are 7.2 × 5.4 and 5.2 × 4.3 mm in diameter and height, respectively; the stalk of the larger one is 1.1 (1.0-1.3) (n = 12) mm in diameter. The piece of thick stalk received from NIWA is 72 mm long and 3.0 (2.8-3.3) (n = 12) mm in diameter, approximately the same gauge as the convoluted stalk shown in the in situ and deck images. Surfaces of the body are a bit lumpy and fuzzy (Fig. 14D); that of the thin attached stalks is also fuzzy. There are no projecting prostal spicules. Colour of the body in life is white, and the stem pale brown; when preserved in ethanol it is very pale brown, almost white.
Skeleton. Choanosomal skeleton of the body is a network of diactins and hexactins. There is no evidence of fusion between any spicules within the body. Spicule fusion is restricted to the choanosomal diactins of the hollow stalks where the diactins are joined by synapticula and points of spot contacts between spicules. Microscleres are scattered evenly throughout the choanosome. Ectosomal skeleton of the dermal and atrial sides of the body and living stalks consists of tightly packed pinular pentactins and very few pinular hexactins (1.3% of 374 assessed). These are supported on, respectively, hypodermal and hypoatrial pentactins which are never raised above the surfaces. Microscleres are present as in the choanosome.
Spicules. Megascleres ( Fig. 15; Table 8) are hypodermal and hypoatrial pentactins, choanosomal hexactins and diactins, and pinular pentactins and a few pinular hexactins. Hypodermal pentactins of the body (Fig. 15A) are regular and usually smooth except for spined ray ends; 31% have macrospines on the central part of the proximal ray. The proximal rays are longer, averaging 1.21 × the length of tangential rays. Hypoatrial pentactins of the body (Fig. 15B) are regular and spined on both tangential and proximal ray ends; macrospines are present on the central part of most (60%) proximal rays but all tangential rays lack macrospines. The proximal ray is longer, on average 1.86 × the length of tangential rays. Hypodermal pentactins of the stalk (Fig. 15C) are regular in shape but significantly smaller than those of the body; they are spined on ray ends but macrospines are uncommon (12%) on the central part of only the proximal rays. Proximal rays are generally longer, on average 1.49 × tangential ray length. Choanosomal hexactins (Fig.  15D) are restricted to the body; rays are smooth, and spines are restricted to the ray ends. Macrospines are never found in the central part of these spicules. Choanosomal diactins (Fig. 15E) are straight or slightly curved and are smooth except for ends; they have small but detectable central swellings. Dermal pinular pentactins of the body (Fig. 15F) have narrow pinular rays topped with a short, sharp apical spine. Their basal rays are entirely spined and end in abruptly pointed tips. Approximately 10% of the dermal pinules are hexactine forms. Atrial pinular pentactins of the body (Fig. 15G) have narrow pinular rays like the dermal pinules but with a longer pinular ray (on average 2.1 ×) and longer apical spine; basal rays are like those of the dermal pinules. Stalk pinular hexactins (Fig.  15H) have a pinular ray that is narrow in its basal half but curves to one side and swells in width apically, assuming an overt club-shape. It has no atrial spine since the apex is enfolded by the apical scales. Basal rays are like those of the dermal and atrial pinules.
Microscleres ( Fig. 15; Table 8) are discohexactins, thick-ray discohexasters and thin-ray discohexasters. Discohexactins (Fig. 15I) are the most abundant microscleres; they have rays ornamented with large, reclined spines and a terminal disc with 5-8 marginal teeth. Thick-ray discohexasters (Fig. 15J) are the least abundant microsclere; they are spherical, have 6-9 thorned terminal rays on each smooth primary ray, and terminal discs have 4-8 marginal teeth. Thin-ray discohexasters (Fig. 15J, K) are among the most numerous microscleres, but comparing their abundance with discohexactins is not possible since detection of the two spicule types requires different microscope arrangements. They are semi-stellate with each smooth primary ray supporting 16 (8-28) (n = 16) thorned terminal rays ending in discs with 3-7 marginal teeth.
Etymology. Named for the rhizome-like stem that may form tangled, convoluted stems from which the main bodies arise, the whole creeping along the substrate (serpens, creeping; Latin).
Remarks. The morphological character of all microscleres being discoid, places this species in the subgenus Caulophacus (Caulophacus). In comparing them to the 22 recognised species of this subgenus ( Distribution. Known only from the type locality, the Kermadec Trench slope, north of New Zealand (Fig. 16A).
Habitat. Attached to hard substratum; depth 4819 m. Description. Morphology of the holotype is a compound mass of a thin, convoluted stalk-part, with at least one small mushroom-shaped body branching from it (Fig. 16D, E), and a longer, thicker, upright stalk-part bearing a larger terminal mushroom-shaped body (Fig. 16B, C). The larger upright stalk has six lateral knobs just below the larger body on its stalk (Fig. 16C) whose nature and function are unknown, possibly sites for attachment to a hard substratum, or are new buds. The lower convo- Figure 16. Caulophacus (Caulophacus) ramosus sp. nov., NIWA 126085, distribution, skeleton, and morphology A map of collection location on Kermadec Trench slope B in-situ image of the largest body; the irregular undulating stalk associated with it is largely hidden in accumulated sediment. The green line is 6.24 cm long copied from between laser spots elsewhere in the image C deck image of the large body, which was unavailable for taxonomic description since used for other analyses (image by PJS) D a smaller body (arrowhead) attached presumably to the same stalk but lower in the sinuous section with multiple branching attachments to small cobbles E The same body enlarged to show the plush of long atrial pinular pentactins F cross section of the larger contort white stalk and its central canal. Image B captured by ROV Team GEOMAR, ROV Kiel 6000 onboard RV Sonne (voyage SO254), courtesy of Project PoribacNewZ, GEOMAR, and ICBM. luted stalk part branches into many attachment points, at least eight within a 27 mm length (Fig. 16D). The smaller of the two bodies attached to this stalk system has a felt-like cover of long pinular pentactins on the outer surface (Fig. 16E); we have had no opportunity to examine the larger body. The stalk in all parts is hollow (Fig. 16F). Overall dimension of the larger body in the in-situ image is 45.5 mm in diameter Figure 17. Caulophacus (Caulophacus) ramosus sp. nov., NIWA 126085, spicules A two whole hypodermal body pentactins and enlarged ray tips B two whole hypoatrial body pentactins and enlarged ray ends C a choanosomal hexactin and two enlarged ray tips D t wo whole choanosomal diactins and enlarged ends and central swellings E dermal body pinular pentactin and enlarged ray ends F atrial body pinular pentactin and enlarged ray ends G discohexactin and enlarged ray end H hemidiscohexaster I thin-rayed stellate discohexaster with enlarged secondary ray tuft and a secondary ray. Scale bars in A apply to B-D scales in E apply to F whole microscleres are at the same scale.
with the stalk having a diameter of 5.9 mm at a point 5 mm below the attachment. The smaller specimen is 5.3 mm in diameter and 3.6 mm in height. Stalk diameter varies from 1.0 mm at the short branch joining the small specimen to the convoluted stalk which is mostly ca 1.8 mm thick. The connection of the convoluted part of the stalk to the thicker upright stalk part was not available for assessment. Surfaces of the small body are covered by a villous plush of long pinular pentactins, but there are no special prostalia present. The lower convoluted stalk surfaces appear devoid of any visible surface spicules, but spicule preparations of this apparently "barren" stalk still show that typical stalk spicules are present. Thus, spicules obtained from stalks may derive from other locations on the specimen and should be considered as possibly from other original sources. Surfaces of the upper straight stalk and the terminal larger body are known only from fresh seawater-wet lab photos; they are covered by a thick spiny layer of brown tissue (Fig. 16C). Colour of the body in life is translucent white; when preserved in ethanol it is pale brown.
Skeleton. Choanosomal skeleton of the body is a network of diactins and hexactins. There is no evidence of fusion between any spicules within the body. Spicule fusion is restricted to the choanosomal diactins of the hollow stalks where the diactins are joined by fusion at spot contacts and by relatively long synapticula forming ladders. Microscleres are scattered evenly throughout the choanosome. Ectosomal skeleton of the dermal and atrial sides of the body consists of tightly packed pinular pentactins; no pinular hexactins are present. These are supported on, respectively, hypodermal and hypoatrial pentactins, which are never raised above the surfaces. Microscleres are present as in the choanosome.
Spicules. Megascleres ( Fig. 17; Table 9) are hypodermal and hypoatrial pentactins, choanosomal hexactins and diactins, and pinular pentactins. Hypodermal pentactins of the body (Fig. 17A) are regular and smooth except for spined ray ends. The proximal rays are longer, averaging 1.26 × the length of tangential rays. Hypoatrial pentactins of the body (Fig. 17B) are also regular and smooth except for spined areas on both tangential and proximal ray ends. The proximal ray is longer, averaging 1.41 × the length of tangential rays. Hypodermal pentactins of the stalk (not figured) are regular in shape but significantly smaller than those of the body. Choanosomal hexactins (Fig. 17C) are restricted to the body; rays are smooth and spines are present only on ray ends. Macrospines are never found in the central part of these spicules. Choanosomal diactins (Fig. 17D) are straight or slightly curved and are smooth except for the ends; they have small but detectable central swellings. Dermal pinular pentactins of the body (Fig. 17E) have narrow pinular rays topped with a short, blunt apical spine. Their basal rays are entirely spined and end in abruptly rounded tips. Atrial pinular pentactins of the body (Fig. 17F) have narrow pinular rays like the dermal pinules, but with a longer pinular ray (on average 1.25 ×); however, presence of an apical spine was not determined since all of these examined in SEM had broken tips. Basal rays are like those of the dermal pinules. Stalk pinular pentactins (not figured) are morphologically similar to the dermal body pentactins. Microscleres ( Fig. 17; Table 9) are thick-rayed discohexactins and rare hemidiscohexasters and thin-rayed stellate discohexasters. Discohexactins (Fig. 17G) are the most abundant microscleres; they have rays ornamented with large, reclined spines and a terminal disc with 5-8 marginal teeth. Rare hemidiscohexasters (Fig. 17H) are similar to the discohexactins. Thin-rayed stellate discohexasters (Fig. 17I) have long, smooth primary rays supporting a narrow shorter brush of 3-9 straight, rough, terminal rays ending in small discs.
Etymology. Named for the lower, convoluted stalk part, which branches into many attachment points (ramosus, branching; Latin).
Remarks. The morphological character of all microscleres being discoid, places this species in the subgenus Caulophacus (Caulophacus). In comparing it to the 22 recognised species of this subgenus (Table 7), it is apparent that there are no forms known with all pinules, both dermal and atrial, as exclusively pentactins. It is very like the previous described new species, C. (Caulophacus) serpens sp. nov. in its mainly, but not exclusively, pinular pentactins, and in the body form with a significant portion of the stalk convoluted, attached by many attachment sites and compound bearing several bodies. The two differ, however, in pinule morphology and types of microscleres. Also, molecular data (MD, unpubl. results) suggest a closer relationship of this specimen to C. (Caulophacus) arcticus, C. (Caulodiscus) valdiviae, and C. (Oxydiscus) weddelli than to C. (C.) serpens sp. nov. Since it cannot be assigned to any of the former species on the basis of morphology, it is thus clear that the form described here represents the holotype of a new species named Caulophacus (Caulophacus) ramosus sp. nov.

Conclusions
ith the material described herein, the known diversity of rossellids from the surrounding waters of New Zealand has almost doubled, from previously known nine species in five genera to 17 species in eight genera, including six species and one genus new to science: Sympagella clavipinula Tabachnick & Lévi, 2004Symplectella rowi Dendy, 1924 Descriptions of two further new rossellids (Lanuginellinae) from RV Sonne cruise SO254 could not be completed by HMR and will be reported elsewhere, together with numerous other hexactinellid specimens collected on that cruise.

Obituary
Dr Henry Michael Reiswig of Saanichton, British Columbia, Canada (born 8 July 1936 in St. Paul, Minnesota, USA), died on 4 July 2020 at the age of 83, in his garage laboratory, doing what he loved most: science (Fig. 18). Henry was a marine biologist and globally renowned expert on the glass sponges (Hexactinellida), contributing enormously to knowledge of sponges in general.
Henry began his career at the University of California, Berkeley and completed a PhD at Yale University, after which he served as Professor of Biology at McGill University and Redpath Museum, Montreal, from 1972, until he officially retired in 2001. Those who knew him well chuckled at his 'retirement': in 2020 he was still hard at work describing the glass sponge fauna of New Zealand with his Kiwi and German friends. After formal retirement, he took up 'post-retirement' offices at the University of Victoria and the Royal British Columbia Museum in Victoria, B.C., ever busier and juggling numerous projects with colleagues and students all over the world.
Henry leaves an enormous legacy: his beloved wife, Ann, who died in February 2019 and their three wonderful daughters, Jennifer, Penelope, and Amy; more than 100 publications including journal articles, book chapters, and conference presentations; several sponge species and a sponge-derived secondary metabolite named after him, and hundreds of research colleagues and students who loved and respected him.
Henry also leaves a huge legacy at the National Institute of Water and Atmospheric Research (NIWA), New Zealand. He first began his work on New Zealand glass sponges in the 1980s as a visiting scientist at NIWA. Dr Dennis P. Gordon, now emeritus at NIWA, and then editor of the NIWA Biodiversity Memoir series, encouraged Michelle's involvement and working with Henry, helping him make progress on this dauntingly huge project: to identify and name more than 329 glass sponges that had been collected by the original New Zealand Oceanographic Institute. With a sense of trepidation, Michelle began to work closely with Henry, ably assisted by the NIWA Invertebrate Collection manager, Sadie Mills. The current collection now includes more than 2000 glass sponges, most examined by Henry. Together we were able to get two major NIWA Biodiversity Memoirs, on the dictyonal and euplectellid glass sponges, over the line, and were in the process of describing the last two big groups, the Rossellidae and Amphidiscophora, when the shocking news arrived.
How do we go on? Well, continue in his name we do. Henry was utterly dedicated to his work and had a formidable intellect; for all his profound knowledge, he was also slightly 'weird' and wonderful, and there was nothing more fun than sitting with Henry, after a conference lecture, enjoying a cool beer in the sunshine. In the words of his official family obituary, he was, "a rascal, a scholar, a deeply moral man, and is profoundly and deeply missed."