Schendylops ramirezi, Pereira, 2013

Pereira, Luis Alberto, 2013, Discovery Of A Second Geophilomorph Species (Myriapoda: Chilopoda) Having Twenty-Seven Leg-Bearing Segments, The Lowest Number Recorded Up To The Present In The Centipede Order Geophilomorpha, Papéis Avulsos de Zoologia (São Paulo) 53 (13), pp. 163-185 : 163-185

publication ID

https://doi.org/ 10.1590/S0031-10492013001300001

persistent identifier

https://treatment.plazi.org/id/7E7CED52-FFD8-5232-FF09-5A71FB32D5F0

treatment provided by

Felipe

scientific name

Schendylops ramirezi
status

sp. nov.

Schendylops ramirezi sp. nov.

( Figs. 1-60 View FIGURES 1‑7 View FIGURES 8‑12 View FIGURES 13‑17 View FIGURES 18‑20 View FIGURES 21‑26 View FIGURES 27‑35 View FIGURES 36‑41 View FIGURES 42‑45 View FIGURES 46‑55 View FIGURES 56‑60 )

Diagnosis: A Neotropical species of Schendylops without pore-field on sternite of the first leg-bearing segment; pore-fields present on anterior region of the body only; all pore-fields undivided; a.a. IV similar in length to the contiguous a.a.; medial edge of forcipular trochanteroprefemur unarmed.

Among the Neotropical species of the genus, these five combined traits are also present in S. anamariae (Pereira, 1981) ; S. interfluvius (Pereira, 1984) ; S. janauarius ( Pereira, Minelli & Barbieri, 1995) ; S. jeekeli Pereira, 2009 ; S. lomanus (Chamberlin, 1957) , S. nealotus (Chamberlin, 1950) ; S. oligopus ( Pereira, Minelli & Barbieri, 1995) ; S. pallidus (Kraus, 1955) ; S. paolettii (Pereira & Minelli, 1993) ; S. perditus (Chamberlin, 1914) and S. virgingordae (Crabill, 1960) .

For a confident identification of the present new species it may be compared in detail with S. oligopus with which it shares the lowest segment numbers in the genus Schendylops , and a very small body size. S. ramirezi sp. nov. can be differentiated from S. oligopus by means of the following selected traits (those for the latter are given in parentheses): male with 27 leg-bearing segments, female with 29 (male with 27 or 29 leg-bearing segments, female with 31); body length up to 7 mm (body length up to 10 mm); clypeus without a clypeal area, Fig. 47 View FIGURES 46‑55 (clypeus with an anterior middle area with areolation smaller than the remaining clypeal surface, Fig. 62 View FIGURES 61‑66 ); coxosternite of first maxillae with 1+1 setae, Fig. 51 View FIGURES 46‑55 (coxosternite of first maxillae devoid of setae, Fig. 65 View FIGURES 61‑66 ); coxosternite of second maxillae bearing a large seta on the middle, Fig. 51 View FIGURES 46‑55 : a (coxosternite of second maxillae without a seta on the middle, Fig. 65 View FIGURES 61‑66 ); single pore-fields accompanied at the anterior sides by a few additional pores, Figs. 28-41 View FIGURES 27‑35 View FIGURES 36‑41 (pore-fields not accompanied at the anterior sides by additional pores, Figs. 67-73 View FIGURES 67‑76 ); pretarsus of ultimate legs as a very small tubercle with a single apical spine, Figs. 44, 45 View FIGURES 42‑45 (pretarsus as a very small tubercle with two apical spines, Fig. 75 View FIGURES 67‑76 ).

Other morphological traits included in Table 1 differentiate S. ramirezi from S. oligopus .

Among the other species mentioned above, those having a range of leg-bearing segments roughly similar to S. ramirezi are S. interfluvius ; S. janauarius ; S. jeekeli ; S. lomanus ; S. paolettii and S. perditus . (For characters differentiating S. ramirezi from these latter species, see Discussion below).

Type material examined: All specimens from Brazil: RJ: Ilha Grande, Praia Grande das Palmas, 19-21 January 1999, M.J. Ramírez leg.: holotype female, 29 l. -b.s., b.l. 7 mm; paratype A (male), 27 l. -b.s., b.l. 5 mm; paratype B (male), 27 l. -b.s., b.l. 6 mm; paratype C (female), 29 l. -b.s., b.l. 6.5 mm; paratype D (female), 29 l. -b.s., b.l. 7 mm; paratype E (male), 27 l. -b.s., b.l. 5 mm.

Remarks: Mandibles of paratype “D” in a permanent microscope slide (remaining body parts in alcohol); holotype and other paratypes in alcohol.

Depository of types: MZUSP .

Other material examined: All specimens from the same locality, date and collector as the type series : 3 males (sub-adult), 27 l. -b.s., b.l. 4.5, 4.5, and 4.5 mm; 2 females (subadult), 29 l. -b.s., b.l. 4.5, 4.5 mm; 13 juvenile females (with 1+1 coxal organs only), 29 l. - b.s., b.l. 3, 3, 3, 3, 3, 3.5, 3.5, 3.5, 3.5, 3.5, 4, 4, and 4 mm; 1 juvenile male (with 1+1 coxal organs only), 27 l. -b.s., b.l. 3 mm ( MZUSP) .

Remarks: The adult condition of all females in the type series is indicated by the two spermathecae full of spermatozoa ( Fig. 27 View FIGURES 27‑35 : a). As for the three male paratypes, no mature spermatozoa have been detected in their tubula seminifera, nevertheless (except for the ultimate leg-bearing segment and postpedal segments) all other morphological traits are similar to those of the female holotype and female paratypes; the penis has a fully developed aspect ( Fig. 60 View FIGURES 56‑60 ), and the coxal organs are completely developed, all these elements being indications of their adult condition.

Male paratypes A and E (5 mm long) have the same morphological attributes as the male paratype B (6 mm long).

Among the juveniles provided with 1+1 coxal organs only, it is possible to distinguish the male from the females on the basis of the different position and shape of the tiny immature gonopods.

Female holotype: twenty nine leg-bearing segments, body length 7 mm, maximum body width 0.37 mm; cephalic plate: length 0.27 mm, maximum width 0.22 mm; maximum width of forcipular coxosternite 0.24 mm. Ground color (of preserved specimen in alcohol) pale yellowish.

Antennae: relatively short, ca. 2.40 times as long as the cephalic plate, distally not attenuate. Length/ width ratio of left a.a. I-XIV as follows: I (0.76: 1); II (1.13: 1); III (1.08: 1); IV (1.10: 1); V (0.99: 1); VI (1.0: 1); VII (0.94: 1); VIII (0.87: 1); IX (0.87: 1); X (0.88: 1); XI (0.81: 1); XII (0.68: 1); XIII (0.62: 1); XIV (1.91: 1). Ratio of width of a.a. II /width of a.a. XIV (1.0: 1). Ventral chaetotaxy: setae on a.a. I to V of different lengths and few in number, those of remaining articles progressively shorter and more numerous towards the tip of the appendage ( Figs. 1, 2 View FIGURES 1‑7 ). Apical a.a. with 7 claviform sensilla on the external border and two on the internal border ( Fig. 3 View FIGURES 1‑7 ); distal end of this a.a. with ca. 4 small hyaline specialized sensilla apparently not split apically ( Fig. 3 View FIGURES 1‑7 ). Ventral and dorsal surface of a.a. II ( Figs. 4 View FIGURES 1‑7 , 8 View FIGURES 8‑12 ), V ( Figs. 5 View FIGURES 1‑7 , 9 View FIGURES 8‑12 ), IX ( Figs. 6 View FIGURES 1‑7 , 10 View FIGURES 8‑12 ) and XIII ( Figs. 7 View FIGURES 1‑7 , 11 View FIGURES 8‑12 ) with very small specialized sensilla. Ventral sensilla of two types (a and b). Type a sensilla very thin and not split apically ( Figs. 5-7 View FIGURES 1‑7 : a), type b sensilla very similar to those of the apex of the terminal a.a., not split apically on a.a. II ( Fig. 4 View FIGURES 1‑7 : b) but are divided in two tiny apical branches on a.a. V, IX and XIII ( Figs. 5-7 View FIGURES 1‑7 : b). Specialized sensilla on dorsal side represented by three different types: a and b similar to a and b of ventral side and type c sensilla, bigger, not divided apically and darker (ochreous in color) ( Fig. 11 View FIGURES 8‑12 : a, b, c). Relative position of specialized sensilla on ventral and dorsal surfaces of the specified a.a. as in Figs. 4-7 View FIGURES 1‑7 and 8-11 View FIGURES 8‑12 respectively. Distribution of type a, b, and c sensilla as in Table 2 .

Cephalic plate: slightly longer than wide (ratio 1.19: 1), anterior border convex, posterior border concave, lateral margins curved. Shape, areolation, and chaetotaxy

as in Fig. 12 View FIGURES 8‑12 . Ratio of maximum width of cephalic plate/maximum width of forcipular tergite, 1.24: 1.

Clypeus: chaetotaxy represented by 1+1 postantennal setae, 4+3 setae distributed on a middle transversal band (of which 1+1 are placed in a lateral position, Fig. 13 View FIGURES 13‑17 : a), and 1+1 prelabral setae ( Fig. 13 View FIGURES 13‑17 ). Surface of clypeus without a clypeal area (similar to female paratype D, Fig. 47 View FIGURES 46‑55 ).

Labrum: with nine dark and short teeth on the central arc, lateral pieces with 2+2 less sclerotized teeth, each with a very sharp medial extension ( Fig. 14 View FIGURES 13‑17 ).

Mandible: dentate lamella apparently not subdivided into blocks, with ca. 8-9 teeth (similar to female paratype D, Figs. 49, 50 View FIGURES 46‑55 ); pectinate lamella with ca. 11-12 teeth.

First maxillae (similar to female paratype D, Figs. 51, 52 View FIGURES 46‑55 ): with lappets on the coxosternite and telopodites, those of coxosternite smaller than the latter. Coxosternite with 1+1 setae; coxal projections round-tipped and provided with 1+1 setae. Article II of telopodites with 1+1 setae on ventral side and 2+2 sensilla on dorsal side.

Second maxillae (similar to female paratype D, Figs. 51, 53-55 View FIGURES 46‑55 ): coxosternite with 1 large seta on the middle ( Fig. 51 View FIGURES 46‑55 : a) and 5+5 smaller lateral setae. Apical claw of telopodites well developed, bipectinate, ventral edge with 4 teeth, dorsal edge with 6 teeth.

Forcipular segment: when closed, the telopodites do not reach the anterior margin of the head ( Fig. 15 View FIGURES 13‑17 ). Forcipular tergite with anterior margin concave, lateral margins curved ( Fig. 12 View FIGURES 8‑12 ); chaetotaxy represented by an irregular transverse median row of eight large setae, and 2+2 lateral much smaller setae distributed near the posterior margin ( Fig. 12 View FIGURES 8‑12 ). All articles of the telopodites without sclerotized teeth ( Fig. 15 View FIGURES 13‑17 ). Tarsungulum with a small pale round-tipped prominence on the basal internal edge. Medial edge of trochanteroprefemur and tibia with diminutive sensilla ( Figs. 19, 20 View FIGURES 18‑20 ). Ventral internal edge of tarsungulum with shape as in Figs. 15, 16 View FIGURES 13‑17 , 18 View FIGURES 18‑20 . Poison glands unusually large (shape and relative size as in Fig. 15 View FIGURES 13‑17 ). Calyx of poison gland very small, shape as in Figs. 16, 17 View FIGURES 13‑17 . Shape and chaetotaxy of coxosternite and telopodites as in Fig. 15 View FIGURES 13‑17 .

Legs (pair 1 to penultimate): first pair shorter and narrower than the second pair, in the proportion of ca. 0.86: 1 ( Figs. 21, 22 View FIGURES 21‑26 ). Chaetotaxy of legs similar throughout the entire body length. Distribution, number, and relative size of setae as in Figs. 21-25 View FIGURES 21‑26 . Claws ventrobasally with three thin and pale accessory spines (one anterior and two posterior), with relative size as in Fig. 26 View FIGURES 21‑26 .

Sternites of leg-bearing segments 1 to penultimate: pore-fields present from sternite 2 to 15 inclusive (wholly absent on the remaining sternites). All pore-fields undivided. Fields accompanied by one-two additional pores at one or both sides of the anterior edge. Shape and relative size of fields changing along the trunk as in Figs. 28-41 View FIGURES 27‑35 View FIGURES 36‑41 . Number of pores as follows: sternite 2 (1+4+2 pores); 3 (1+6+1); 4 (1+10+1); 5 (1+8+1); 6 (1+11+1); 7 (1+8+1); 8 (1+8+1); 9 (2+7+1); 10 (1+6+1); 11 (1+3+1); 12 (1+6+1); 13 (0+5+1); 14 (1+3+0); 15 (1+3+0).

Ultimate leg-bearing segment: intercalary pleurites absent at both sides of the ultimate pretergite ( Fig. 42 View FIGURES 42‑45 ). Ultimate presternite not divided along the sagittal plane; length/width ratio of the tergite, 0.80: 1; length/ width ratio of the sternite 0.70: 1. Shape and chaetotaxy of tergite and sternite as in Figs. 42, 43 View FIGURES 42‑45 . Coxopleura slightly protruding at their distal-internal ventral ends, chaetotaxy represented by a very few large setae distributed as in Figs. 42, 43 View FIGURES 42‑45 . Two single (“homogeneous”) coxal organs in each coxopleuron, both organs unilobed, anterior organ smaller than the posterior in the proportion shown in Figs. 42, 43 View FIGURES 42‑45 , 46 View FIGURES 46‑55 . Relative size of coxal organs in respect to the size of coxopleura and sternite as in Fig. 43 View FIGURES 42‑45 . Coxal organs open on the membrane between coxopleuron and sternite, partially covered by the latter ( Fig. 43 View FIGURES 42‑45 ). Ultimate legs composed of seven articles. Ratio of width of tibia/width of tarsus I, ca. 1.14: 1; ratio of length of tarsus II /length of tarsus I, ca. 1.0: 1. Ratio of length of telopodites of ultimate legs/length of sternite, ca. 3.83: 1. Shape and chaetotaxy of ultimate legs as in Figs. 42, 43 View FIGURES 42‑45 . Ultimate pretarsus represented by a rudimentary terminal tubercle with one diminutive apical spine ( Figs. 44, 45 View FIGURES 42‑45 ).

Postpedal segments: intermediate tergite with posterior margin strongly convex ( Fig. 42 View FIGURES 42‑45 ), intermediate sternite with posterior margin straight, curved on the sides; first genital sternite with posterior margin medially convex, laterally straight to very slightly concave ( Fig. 43 View FIGURES 42‑45 ). Gonopods uniarticulate ( Fig. 43 View FIGURES 42‑45 ).

Male paratype A: twenty-seven leg-bearing segments, body length 5 mm, maximum body width 0.30 mm. All features similar to those in the female except for the shape and chaetotaxy of the ultimate leg-bearing segment and postpedal segments.

Ultimate leg-bearing segment: tergite and sternite trapezoidal, length/width ratio of tergite 0.63: 1; length/ width ratio of sternite 0.60: 1. Shape and chaetotaxy of tergite and sternite as in Figs. 56, 57 View FIGURES 56‑60 . Coxopleura slightly protruding at their distal-internal ventral ends; chaetotaxy represented by a few large setae distributed as in Figs. 56, 57 View FIGURES 56‑60 . Articles of ultimate legs moderately inflated, with shape and chaetotaxy as in Figs. 56, 57 View FIGURES 56‑60 . Ratio of width of tibia/width of tarsus I, ca. 1.14: 1; ratio of length of tarsus II /length of tarsus I, ca. 1.0: 1. Ratio of length of telopodites of ultimate legs/length of sternite ca. 4.20: 1.

Postpedal segments: intermediate tergite with posterior margin convex ( Fig. 56 View FIGURES 56‑60 ), intermediate sternite with posterior margin medially straight, laterally slightly curved, first genital sternite with posterior border slightly convex ( Fig. 57 View FIGURES 56‑60 ). Gonopods biarticulate, basal article with a single seta, apical article without setae ( Figs. 57-59 View FIGURES 56‑60 ), penis without apical setae, shape as in Fig. 60 View FIGURES 56‑60 .

Variation: Antennal article XIV bearing ca. 2-3 claviform sensilla on the internal edge and ca. 7-8 sensilla on the external edge.

In all adult specimens examined, the pore-field series starts on sternite 2 but the posterior limit varies between sternites 13 and 15.

All females have 29 leg-bearing segments, all males 27.

Post-embryonic variation of pilosity of coxosternite of first maxillae: All juveniles having 1+1 coxal organs only, lacking setae on the coxosternite of the first maxillae; conversely, all specimens with 2+2 coxal organs

have setae on this coxosternite: 0+1 or 1+ 1 in the sub-adults, and 1+ 1 in all adults.

Post-embryonic variation of pilosity of coxosternite of second maxillae: All juvenile specimens having 1+1 coxal organs only, lacking a central seta on the coxosternite of the second maxillae; conversely, all specimens having 2+2 coxal organs (sub-adults and adults) bear that seta ( Fig. 51 View FIGURES 46‑55 : a).

Remarks: Pereira et al., (1995) is the original source for the nomenclature of the three types of specialized sensilla (a, b, and c) present on a.a. II, V, IX and XIII.

Male paratypes A and E (5 mm long), having the same form and pilosity of gonopods, shape of penis, and shape and pilosity of ultimate leg-bearing segment and postpedal segments, as the male paratype B (which is 6 mm long).

Etymology: The species is respectfully dedicated to the collector of all type and non-type specimens herein described, Dr. Martín Javier Ramírez, researcher of CONICET, working at the Museo Argentino de Ciencias Naturales “Bernardino Rivadavia”, Buenos Aires, Argentina.

Ecology: The locality in which all specimens herein described have been collected is part of the Atlantic Rainforest biome.

Type locality: Brazil: RJ: Ilha Grande, Praia Grande das Palmas.

Known range: Only known from the type locality.

MZUSP

Museu de Zoologia da Universidade de Sao Paulo

V

Royal British Columbia Museum - Herbarium

VI

Mykotektet, National Veterinary Institute

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