Guipuzcosoma reipi, Antić & Mauriès, 2022

Antić, Dragan & Mauriès, Jean-Paul, 2022, Two new species of the previously monospecific genus Guipuzcosoma Vicente & Mauriès, 1980 from Spain, with establishment of Guipuzcosomatidae fam. nov. (Diplopoda: Chordeumatida), Zootaxa 5093 (2), pp. 142-168 : 156-163

publication ID

https://doi.org/10.11646/zootaxa.5093.2.2

publication LSID

lsid:zoobank.org:pub:31913C5B-A8D5-4A30-8D9E-4C7C9E953E1E

DOI

https://doi.org/10.5281/zenodo.5906898

persistent identifier

https://treatment.plazi.org/id/03E387B4-FFC9-CD19-56C4-0AC6FCA0FCDE

treatment provided by

Plazi

scientific name

Guipuzcosoma reipi
status

sp. nov.

Guipuzcosoma reipi sp. nov.

Figs 7–12 View FIGURE 7 View FIGURE 8 View FIGURE 9 View FIGURE 10 View FIGURE 11 View FIGURE 12

Diagnosis. Differs from both congeners in the structure of angiocoxites 1, whose distal processes are sigmoid vs. distal processes reduced, with lateral bumps in G. comasi , or almost the same width in its entire length, with an acuminate distal part bent laterad in G. karinae sp. nov. The anterior part of the medial bursal structure of the vulvae in G. reipi sp. nov. is quadrangular with straight lateral margins, vs. heart-shaped in G. comasi or subquadrangular with convex lateral margins in G. karinae sp. nov. Additionally, G. reipi sp. nov. differs from G. comasi by subtriangular vs. rounded lateral parts of colpocoxites in posterior view, or by more differentiated coxal processes on leg-pairs 7 and 11 compared to G. karinae sp. nov. Significant differences also exist in the shape of the posterior part of the medial bursal structure of the vulvae in all three species.

Name. The new species is named in honour of colleague and friend, myriapodologist Hans Reip (SMNG), one of the collectors. A noun in the genitive case.

Material examined (7 ♂♂, 4 ♀♀, 2 juveniles).

Holotype: SPAIN ● ♂; Alava province , Montes de Altzania , Sierra de Urquilla , south of mountain chain Aikorriko Mendikatea , south west of Mountain Aitzgorri , north of end of road from Salvatierra-Ordonana-ZalduondoZumarraundi, north of Zumarraundi, deep gryke with stream discharge (cave), in the lower third, 42.9241, -2.3224, 980 m a.s.l., Fagus forest, thick leaf layer, in leaf litter; 24. April 2009; K. Voigtländer leg.; SMNG. GoogleMaps

Paratypes: SPAIN ● 1 ♂; same data as for holotype; SMNG GoogleMaps 1 ♀; same data as for holotype but near the entrance of cave, Fagus leaves; SMNG GoogleMaps 1 ♂, 1 ♀, 2 juveniles; Gipuzkoa province , Sierra de Aralar , Beasain , road from Lazkao to Etxarri-Aranaz, western Pass, 42.9572, -2.1122, 550 m a.s.l., Fagus forest, in leaf litter; 21 April 2009; H. Reip, K. Voigtländer leg.; SMNG GoogleMaps 1 ♂, 1 ♀ (used for SEM); same data as previous; NHMW MY10255 View Materials (♂) GoogleMaps , MY10254 (♀) ● 1 ♂, 1 ♀; same data as previous; IZB GoogleMaps 1 ♂; Gipuzkoa province , Montes de Altzania , Sierra de Urquilla , south of mountain chain Aikorriko Mendikatea , south west of Mountain Aitzgorri, north of end of road from Salvatierra-Ordonana-Zalduondo-Zumarraundi, southern lower edge of slope to valley plain Aldasbarreneta, 42.9427, -2.3346, 1120 m a.s.l., lower edge of doline, ca. 1 m above ground of doline, Fagus forest, under stones in deep humus and leaf layer; 24 April 2009; H. Reip leg.; SMNG GoogleMaps 1 ♂; Gipuzkoa province , Sierra de Aralar , Tolosa , south of Bedaio / Goikoa, 43.0494, -2.0400, 420 m a.s.l., farm buildings and stone wall, logs, wood, stones and rubble, under stones and logs; 21 April 2009; H. Read leg.; NHM GoogleMaps .

Description. SIZE AND NUMBER OF BODY RINGS. Body in adults with 30 rings (including telson). Holotype male 10 mm long, vertical diameter of the largest ring 0.8 mm. Paratype males 7.8–9.7 mm long, vertical diameter of the largest ring 0.65–0.7 mm. Paratype females 8.5–10 mm long, vertical diameter of the largest ring 0.75–0.8 mm.

COLORATION ( Fig. 7 View FIGURE 7 ). Variable. From yellowish-brown to darker brown, with greyish patterns. Ventral halves lighter. Ommatidia blackish.

HEAD ( Figs 7B, C View FIGURE 7 , 8A–C View FIGURE 8 ). Setose, frontal side slightly concave in males, convex in females. Labrum with three medial teeth and 5+5 labral and 2+2 supralabral setae ( Fig. 8A View FIGURE 8 ). Promentum subtriangular, without setae. Lingual plates with 4–6 setae arranged in one or two rows. Stipites with ca. 20 setae each.Antennae 1.4 mm long in holotype male. Length of antennomeres (in mm): I (0.07), II (0.17), III (0.37), IV (0.18), V (0.34), VI (0.13), VII (0.12) and VIII (0.04). Length/breadth ratios of antennomeres I–VII: I (1), II (2), III (4), IV (2), V (3.5), VI (1) and VII (1.3). Antennomeres II, IV, V, VI and VII with one, three, one, four and one sensillum trichoideum, respectively ( Fig. 8C View FIGURE 8 ). Lateral to antennal sockets a group of papillae-like outgrowths present ( Fig. 8A, B View FIGURE 8 ). Number of ommatidia: 13 in 4 rows in both sexes, arranged in irregular subtriangle ( Fig. 8B View FIGURE 8 ).

COLLUM. Narrower than head, with six macrochaetae, as all body rings. Anterior edge semi-circular, posterior margin gently concave.

BODY RINGS ( Figs 7 View FIGURE 7 , 8D–F View FIGURE 8 ). With lateral humps. Macrochaetae long and trichoid ( Fig. 8D–F View FIGURE 8 ). CIX (ring 15) = 1; MIX (ring 15) ~ 2; PIX (ring 15) = 0.8; MA (ring 15) ~ 110˚. Prozonites with hexagonal tiles. Metazonites dorsally with scale-like structures, lateroventrally striated. Lateral parts of humps smooth.

TELSON. Epiproct with a pair of spinnerets and 3+3 setae (1+1 paramedian, 2+2 marginal). Hypoproct with 1+1 distal setae. Paraprocts with 3+3 marginal setae in distal part.

LEG- PAIRS 1 AND 2. In both sexes with tarsal combs; femora with several long and robust setae; postfemora and tibiae each with several long and robust setae arranged in a group.

MALE SEXUAL CHARACTERS ( Fig. 9B–C View FIGURE 9 ). Leg-pair 2 with genital openings on coxae. Leg-pairs 3–7 enlarged compared to leg-pairs 1 and 2. Coxa 7 with mesal bump directed posterolaterad ( Fig. 9B View FIGURE 9 ). No other peculiarities on pregonopodal legs. Leg-pair 10 with coxal sacks and with short triangular trochanteral bumps ( Fig. 9C View FIGURE 9 ). Leg-pair 11 with coxal sacks and with short nippled slender coxal process ( Fig. 9D View FIGURE 9 ).

ANTERIOR GONOPODS ( Figs 9E View FIGURE 9 , 10A–F View FIGURE 10 , 11A–D View FIGURE 11 ). Gonopodal sternum (S) poorly developed, mainly membranous, distomedial parts forming subtriangular structures around round aperture and merging with gonopods. Coxites (Cx) more or less spoon-shaped, wide in lateral view, supporting two pairs of angiocoxites. Anteromedial pair (= angiocoxite 1) (A1) widest in mid-height, its mesoproximal sides accommodate shape of sternal triangle; distal process (dA1) sigmoid with distal parts curved laterad; posterior process (pA1) strongly developed, somewhat claw-like in lateral view with small denticles on posterior margin, skintight to lateral sides of distal extension of colpocoxite (deC). Angiocoxites 2 (A2) divided into two branches, anterior branch (aA2) consisting of several flagelloid processes with denticulated posterior margins distally; posterior branch (pA2) long, acuminate, with longitudinal striations, leans on flagelloid processes closing a canal between; both pA1 and pA2 are directed mesad, and slightly posteriad with overlapping distal parts; A2 outgrows all other parts of anterior gonopods. Colpocoxites (C) massive, strongly developed, chitinized; consist of smaller basal protrusions (bc) roundish in lateral view and merged with main massive structures whose distal extensions (deC) are in form of elongated horns strongly bent anteriad and skintight to mesal sides of pA1; posterior mesal protrusions (pC) rounded and laterally flattened with circular membranous remnants (ms) on lateral sides. Between A2 and C, laterally, well-developed structure with large number of long, branched hair-like outgrowths (ho) presents.

POSTERIOR GONOPODS ( Figs 9F View FIGURE 9 , 10G View FIGURE 10 , 11E, F View FIGURE 11 ). Gonopodal sternum (S) poorly developed, membranous, leaving both gonopods almost free; only chitinized part is pair of anterior concave bulges (cb) for accommodation of proximal (basal) parts of posterior gonopods. Coxotelopodites (Ct) massive, without articulation, distally with long setae, while mesally, in upper half, with two striking acuminate horns (h); basomesally with partially chitinized colpocoxites (C) both mainly with one long distal seta and slightly serrated mesal margins. Coxotelopodites subdistally with brownish or blackish pigment remnants (pr). Distal half of Ct slightly curved posteromesad.

LEG- PAIR 3 IN FEMALE ( Fig. 9A View FIGURE 9 ). With lateral sternal lobes.

VULVAE ( Figs 10H View FIGURE 10 , 11G View FIGURE 11 ). With a strongly-developed, massive, wrinkled postgenital membranous structure (Pgm) covering posterior and partially lateral parts of bursae (B). Lateral valves of B rounded posteriorly, without denticles and spicule-like outgrowths in distoposterior ⅔; distoanterior ⅓ wrinkled with long setae. Mesal valves of B completely merged, only with anterior fissure as evidence of former separation; anterior ⅔ wrinkled distally with long setae and straight lateral margins with sharp posterior corners; posterior ⅓ separated from rest by deep depression and represents striking unpaired medial structure (mbs) in the form of mushroom. Operculum (O) bilobed.

Remarks. Interestingly, on the SEM micrograph of the vulvae ( Fig. 10H View FIGURE 10 ) in the fissure between the lateral valves and the medial structures (mesal valve), as well as on the surface of the left lateral valve (highlighted square), structures that we consider to be spermatozoa can be seen. These structures ( Fig. 10I, J View FIGURE 10 ) are about 12 µm in diameter, and are characterized by a narrow medial protuberance, which rises from the coin-like structure. The medial protuberance could be an acrosome-containing structure, while the basal structure would contain a nucleus. If we are right, these could be the first photographs of spermatozoa in the entire order Chordeumatida . These spermatozoa nicely fit the general appearance of spermatozoa in other Diplopoda, whose hypothetical evolution is presented in Bacceti et al. (1979: 102, fig. 14). It is clear that only cytological methods will show whether the spermatozoa of Chordeumatida belong to the so-called monolayered or bilayered acrosome clade.

Distribution. So far, known only from a few localities on the borders between Alava and Gipuzkoa, and Gipuzkoa and Navarre provinces ( Fig. 12 View FIGURE 12 , blue circles).

SMNG

Senckenberg Museum fuer Naturkunde Goerlitz

NHMW

Naturhistorisches Museum, Wien