Antho (Acarnia) ridgwayi, 2019

Stone, Robert P., Lehnert, Helmut & Hoff, Gerald R., 2019, Inventory of the eastern Bering Sea sponge fauna, geographic range extensions and description of Antho ridgwayi sp. nov., Zootaxa 4567 (2), pp. 236-250 : 245-249

publication ID

https://doi.org/ 10.11646/zootaxa.4567.2.2

publication LSID

lsid:zoobank.org:pub:A5A04DAC-86F1-46AF-BA68-59A7014E6655

DOI

https://doi.org/10.5281/zenodo.5944522

persistent identifier

https://treatment.plazi.org/id/2C6287D2-FFCF-E975-DC8B-FB015B39FE66

treatment provided by

Plazi

scientific name

Antho (Acarnia) ridgwayi
status

sp. nov.

Antho (Acarnia) ridgwayi View in CoL n. sp.

( Figs. 2 View FIGURE 2 & 3 View FIGURE 3 ; Table 2)

Material examined. Holotype GoogleMaps USNM2084685 View Materials , largely intact specimen originally frozen then dried, collected by Jerry Hoff with a research survey bottom trawl from the FV Cape Flattery; 21 June 2016, 210 m depth, haul station #27, 97.5 km WSW of St. Paul Island, Pribilof Islands   GoogleMaps , upper slope of the eastern Bering Sea   GoogleMaps (56°54.5880' N, 173°21.9390' W). Water temperature = 3.9 °C. A fragment of the holotype is deposited at the Zoologische Staatssammlung München, Germany under the registration number ZSM 20190188 View Materials .

Description. A foliaceous or flabellate, golden brown sponge with an irregular outline and lobes in several directions ( Fig. 2A View FIGURE 2 ), maximum dimensions 130 x 120 x 2–3 mm. The consistency is flexible and resilient. No oscules visible, surface is smooth.

Skeletal architecture. The relatively narrow sheet of the sponge has a reticulation of acanthostrongyles in its center ( Figs. 2B View FIGURE 2 & 3A View FIGURE 3 ), near the two surfaces, plumose tracts composed of two categories of styles rise towards the ectosome ( Figs. 2B, 2C View FIGURE 2 , & 3A View FIGURE 3 ). The smaller category of subtylostyles with microspined heads also occurs in bundles in between the tracts. The ectosome consists of a thin organic veneer ( Figs. 2B & C View FIGURE 2 ) and contains abundant palmate isochelae, toxa and tylotes with microspined heads.

Spicules. Megascleres are ectosomal tylotes with microspined heads ( Fig. 3C View FIGURE 3 ), 223–254 x 6–9 µm, choanosomal acanthostrongyles ( Figs. 3B & D View FIGURE 3 ), 195–228 x 14–24 µm, choanosomal, echinating smooth, thick styles ( Figs. 2B, 2D View FIGURE 2 , & 3B View FIGURE 3 ), 620–805 x 2 5–38 µm, and choanosomal thin (subtylo-)styles ( Fig. 3B View FIGURE 3 ) with microspined heads, 378–466 x 8–10 µm. Microscleres are palmate isochelae ( Fig. 3F View FIGURE 3 ), 20–24 µm and toxa in two size categories, small, 10–42 µm, and large, 136–182 µm ( Figs. 2D View FIGURE 2 & 3E View FIGURE 3 ).

Discussion. A well-structured choanosome with megascleres differentiated in geometry and distribution, more than one category of choanosomal megascleres, one greatly modified and accessory spicules that consist of acanthostrongyles and are accompanied by ascending plumose tracts of styles clearly indicate the assignment of the new species within the family Microcionidae , the genus Antho , and the subgenus Acarnia . A comparison of the new species with congeners from the Bering Sea, North Pacific Ocean, Arctic Ocean, and North Atlantic Ocean indicate that there are no other Antho species in the area with two categories of toxa and none with large styles of comparable size and geometry. The new species differs from all compared congeners in the following characters ( Table 2):

Antho arctica has thinner large styles that have spined heads, much thinner acanthostrongyles (approximately one third), tornotes instead of tylotes that are much longer, and lacks toxa.

A. bakusi has shorter styles, an additional category of thin styles and shorter acanthostyles, shorter and thinner acanthostrongyles, no ectosomal tylotes, and three distinct categories of toxa.

A. circonflexa has acanthostyles instead of styles that are shorter and thinner, lacks a second category of styles, much shorter acanthostrongyles, lacks tylotes although the subtylostyles mentioned by Lévi (1960) could be regarded as tylotes based on the figure in the publication, and has shorter isochelae.

A. coriacea has shorter styles (both acanthostyles), much shorter acanthostrongyles, and lacks tylotes although we regard the subtylostyles mentioned by Lévi (1960) as ectosomal spicules.

A. elegans has much shorter styles and acanthostyles, shorter acanthostrongyles, ectosomal subtylostyles intead of tylotes, shorter isochelae, and different sizes of the two toxa categories.

A. illgi has shorter and thinner styles (both categories), short styles without microspined heads, shorter and thinner acanthostrongyles, and lacks tylotes.

A. planoramosa has only one category of styles (acanthostyles), thinner acanthostrongyles spined only at the ends, and lacks toxa.

A. signata has shorter and thinner acanthostrongyles, ectosomal subtylostyles instead of tylotes, anisochelae and only one category of toxa.

A. spinulosa has shorter and thinner thick styles with microspined heads, more slender thin styles that do not have microspined heads, strongyles to tylotes (with spines at the ends only) rather than acanthostrongyles, lacks ectosomal tylotes, smaller isochelae (described as arcuate by Tanita), and only one category of toxa in a size category intermediate to the two in A. ridgwayi .

Etymology. We name this new species in memory of Michelle Ridgway who made major contributions to the conservation of Alaska’s marine resources, particularly in the Bering Sea, and whose passion inspired many.

GBIF Dataset (for parent article) Darwin Core Archive (for parent article) View in SIBiLS Plain XML RDF