Mesobiotus vulpinus sp. nov., 2024

Tumanov, Denis V., Androsova, Evgenia D., Gavrilenko, Marina D. & Kalimullin, Aidar A., 2024, Integrative description of two new species of the genus Mesobiotus (Eutardigrada, Macrobiotoidea) from Russia, with an updated phylogeny of the genus, European Journal of Taxonomy 947 (1), pp. 20-52 : 33-41

publication ID

https://doi.org/ 10.5852/ejt.2024.947.2619

publication LSID

lsid:zoobank.org:pub:5B9DA044-2842-456C-8339-2D097A24A662

DOI

https://doi.org/10.5281/zenodo.13134097

persistent identifier

https://treatment.plazi.org/id/CC615859-F0A0-49F4-A035-28889F370283

taxon LSID

lsid:zoobank.org:act:CC615859-F0A0-49F4-A035-28889F370283

treatment provided by

Plazi

scientific name

Mesobiotus vulpinus sp. nov.
status

sp. nov.

Mesobiotus vulpinus sp. nov.

urn:lsid:zoobank.org:act:CC615859-F0A0-49F4-A035-28889F370283

Figs 7–13 View Fig View Fig View Fig View Fig View Fig View Fig View Fig ; Tables 4–5

Etymology

Named after the latin name ( Vulpes vulpes ) of the most famous animal inhabiting Russkij Island – the common fox.

Material examined

Holotype

RUSSIA • ♀; Primorsky Krai, Vladivostok, Russkij Island , road to the Kruglaja Bay; 43.01386° N, 131.78838° E; 3 Feb. 2023; A. Kalimullin leg.; moss on tree trunk; SPbU 320(10) . GoogleMaps

Paratypes

RUSSIA • 8 ♀♀, 4 eggs; same data as for holotype; SPbU 320(2–9, 11, 13–15) GoogleMaps 2 adult, 2 eggs; same data as for holotype; SEM stub SPbU Tar_65 GoogleMaps 1 adult; same data as for holotype; ZM FEFU (slide 320(1)) GoogleMaps 1 egg; same data as for holotype; ZM FEFU (slide 320(12)) GoogleMaps .

Morphological description

Adult animals

Body elongated ( Fig. 7 View Fig ) (morphometrics in Table 4, raw morphometric data are provided in the Supp. file 5). Fresh specimens uncolored or whitish with slightly greenish gut content, transparent after fixation in Hoyer’s medium. Black eyes present, often dissolving after slide mounting. Cuticle smooth in LM, with fine uniform sculpture consisting of minute conical granules with pointed apices visible under SEM only ( Fig. 8A View Fig ). All legs with granulated areas consisted of small granules, usually well visible in LM. Legs I–III with small granulated areas on the external surfaces, near the claw bases ( Fig. 8B– C View Fig , black arrowhead), the internal leg surfaces without granulation, with indistinctly demarcated large pulvinus, visible in SEM only ( Fig. 10A View Fig , white arrowhead). Legs IV with better-developed granulation mainly dorsally to the claws ( Fig. 8D–E View Fig , white arrowhead) and around the claw bases ( Fig. 10E, H View Fig , black arrowheads).

Buccal-pharyngeal apparatus of Macrobiotus type ( Fig. 9A View Fig ) with the ventral lamina and ten peribuccal lamellae ( Fig. 8F View Fig ). Oral cavity armature ( OCA) of harmsworthi type (according to Kaczmarek et al. 2020) with three bands of teeth visible in LM. Evident first (anterior) band consists of a wide band of numerous minute teeth visible as dots in LM ( Figs 8F View Fig , white arrow, 9E, G). Second band consists of a row of longitudinally elongated triangular teeth ( Fig. 9D–H View Fig ). Third band comprises three dorsal and three ventral transverse ridges ( Figs 8F View Fig white arrowhead, 9D–H). Medio-ventral ridge often divided in two or three separate teeth ( Fig. 9H View Fig ). Latero-ventral ridges often with strong indentations ( Fig. 9G View Fig ), sometimes almost fragmented to separate teeth. Rare additional teeth are present ventrally, between the second and the third teeth bands ( Fig. 9F–H View Fig ). Pharyngeal bulb with apophyses, three macroplacoids and a large microplacoid ( Fig. 9B–C View Fig ). Macroplacoid length sequence is 2<3 ≤1. First macroplacoid is anteriorly narrowed, third macroplacoid with poorly developed subterminal constriction ( Fig. 9B–C View Fig ).

Claws of Mesobiotus type with minute stalk, distinct distal part of the basal portion, short common tract and developed internal septum, defining a distal part ( Fig. 10B, D–E View Fig ). Primary and secondary branches diverge below the half of the claw height, main branches with well-developed accessory points ( Fig. 10B–F View Fig ). Claws of fourth pair of legs slightly longer than claws of first three pairs of legs ( Fig. 10E View Fig ). All claws with smooth lunules ( Fig. 10B–C, E, G View Fig ). Anterior (internal) and posterior (external) claws of the legs IV are similar in shape ( Fig. 10E View Fig ). Single continuous cuticular bars of characteristic shape (two wide short bars connected by thin angular strip) are present below claw bases of the first three pairs of legs ( Fig. 10B, D View Fig , black arrowhead) with poorly developed muscle attachment points below ( Fig. 10B, D View Fig ). Claws of the legs IV are connected with a poorly sclerified horseshoe-like structure, visible in PhC only ( Fig. 10H View Fig , white arrowhead).

Eggs

No eggs with developed embryos were found, but taking into account that M. vulpinus sp. nov. was the only tardigrade species present in the sample we believe that the adult specimens and the eggs belong to the same species.

Eggs spherical, white, ornamented and laid freely ( Figs 11A View Fig , 12A, C View Fig ; morphometrics in Table 5 View Table 5 ). Chorion with conical processes that can be attributed to the “sharp narrow cones” and “reticular design with “bubbles” morphotypes” (according to Kaczmarek et al. 2020). Egg processes in form of elongated cones with poorly differentiated basal and apical parts ( Figs 11B, E–F View Fig , 12–13 View Fig View Fig ). Processes (with the exception of the elongated apical parts) with bilayered walls, with a net of trabecular structures between the internal and external layers, forming irregular rounded meshes of different size, so the processes seem to be reticulated in LM ( Fig. 11 View Fig ). Apical parts of the processes with bubble-like internal structure ( Fig. 11F View Fig ), rarely bifurcating ( Figs 11E View Fig , 13A View Fig ). Processes surface bears annulations, visible in SEM only ( Figs 12B, D View Fig , 13 View Fig ). Rare large pores (1.4–2.3 µm in diameter), poorly discernible in LM and well-visible in SEM, are present on the basal part of all processes, below the half of the process height, forming a single row ( Figs 11H View Fig , white arrowheads, 12, 13, white arrowheads), Second row of distinctly smaller and more numerous pores is located in the most basal part of each process ( Fig. 13 View Fig , black arrowheads). Process bases with poorly developed, sometimes almost invisible crone of dark thickenings ( Fig. 11C, E–F View Fig ). Egg surface between the processes with distinct polygonal relief consisted of ridges forming hexagonal (rarely pentagonal) cells around each process ( Figs 11C–D View Fig , 12 View Fig ). Points of ridges intersection bears small bulbous processes ( Figs 11B View Fig , 12B, D View Fig , 13B View Fig ). Both ridges and bulbous processes with internal trabecular structures, similar to the main processes walls. Egg surface between the processes bases and the ridges of polygonal relief with a system of smaller radial ridges and pores discernible both in LM and SEM ( Figs 11C–D View Fig , 12B, D View Fig , 13 View Fig ).

Reproduction

No males were found.

DNA sequences

Sequences for all four molecular markers were obtained from two specimens (18S rRNA – OR804461, OR804462, 28S rRNA – OR805140, OR805141, ITS-2 – OR805172, OR805173, COI – OR803040, OR803041; voucher slides SpbU 320(08) and 320(15))

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