Literature DB >> 23794815

A new species of Newportia Gervais, 1847 from Puerto Rico, with a revised key to the species of the genus (Chilopoda, Scolopendromorpha, Scolopocryptopidae).

Arkady A Schileyko1.   

Abstract

A new species of the centipede genus Newportia, Newportia stoevi sp. n., is described from Rio Encantado Cave, Puerto Rico. It differs from all congeners by having sternites distinctly margined laterally and ultimate legs bearing 4 spinous processes on both prefemur and femur, and 2 on tibia. The value of some terms used in the taxonomy of the genus have been analyzed and an amended identification key to the species of Newportia is provided.

Entities:  

Keywords:  Newportia; Newportiinae; external characters; identification key; new species

Year:  2013        PMID: 23794815      PMCID: PMC3677341          DOI: 10.3897/zookeys.276.4876

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

The genus Gervais, 1847 is still poorly known. It is especially so with regards to the Puerto Rican fauna where only two species have hitherto been registered. Silvestri (1908) reported Pocock, 1891 from Coamo Springs, while Chagas and Shelley (2003) recorded Chamberlin, 1918 from two localities – 8.4 mi (13.4 km) SW Luquillo, trail to Minas Falls off hwy. 191, Luquillo Division, CaribPageBreakbean National Forest and from 4 mi (6.4 km) N Villalba, Dona Juaña Recreation Area. To these should be added Chamberlin’s (1950) uncertain record of sp. from Maricao Insular Forest, based on a specimen with missing ultimate legs. Herewith, I describe a new species of recently collected in Puerto Rico by Dr Petar Beron from the National Museum of Natural History, Sofia (NMNHS). The specimen was assigned to and tentatively identified as a new species by Dr Pavel Stoev, curator of Myriapoda at the NMNHS who committed it for further study to me. This specimen differs from all congeners, in the first place, by important traits of the ultimate legs (which are normally developed and have no traces of regeneration) and unusually developed lateral margination of sternites. The identification key to the species of (Schileyko and Minelli 1998) has been updated to accommodate this and other new species described recently (e.g., Chagas & Shelley, 2003), as well as to reflect other nomenclature novelties proposed in the genus. Some general notes on the external anatomy of have been made, too. The terminology follows Bonato et al. (2010).

Systematic part

SCOLOPENDROMORPHA Pocock, 1895

Scolopocryptopidae Pocock, 1896 Newportiinae Pocock, 1896 Gervais, 1847

sp. n.

urn:lsid:zoobank.org:act:AE5E2F31-F3F2-45EB-9AD6-24EDA31D1D66 http://species-id.net/wiki/Newportia_stoevi Figs 1 10
Figures 1–4.

,sp. n. 1 Habitus 2 Head and anterior segments, ventral view 3 Forcipular segment, ventral view 4 Tergites 22 and 23 and prefemora of ultimate legs, dorsal view; (pt) – pretarsus of second maxilla, (ar3) – article 3 of telopodite of second maxilla, (cxs) – forcipular coxosternite, (am) – anterior margin of coxosternite, (t) – tarsungulum, (ps) – paramedian sutures, (lls) – lateral longitudinal sutures, (ut) – tergite of ultimate leg-bearing segment, (sup) – spurs of ultimate prefemur.

Figures 5–8.

,sp. n. 5 Segments and midbody legs, ventral view 6 Posterior body end, ventral view 7 Left side of ultimate leg-bearing segment and prefemora of ultimate legs, ventro-lateral view 8 Ultimate legs, ventro-lateral view; (mls) – median longitudinal sulcus, (ls) – lateral sutures, (lm) – lateral margination, (s) – setae, (tl) – monoarticulated tarsus of locomotory leg, (us) – sternite of ultimate leg-bearing segment, (cx) – coxopleuron, (cxp) – coxopleural process, (pm) – posterior margin of pleuron of ultimate leg-bearing segment, (vsp) – ventral spinous processes of ultimate prefemur, (p) – prefemur, (f) – femur, (t) – tibia, (t1) – tarsus 1, (t2) – tarsus 2.

Figures 9–12.

,sp. n. 9 Femora, tibiae and tarsi 1 of ultimate legs, dorsal view 10 Femora, tibiae and tarsi 1 of ultimate legs, ventral view; Chamberlin, 1922 11 Forcipular segment, ventral view (after Schileyko and Minelli 1998); Chamberlin, 1921 12 Ultimate legs, dorso-lateral view (after Schileyko and Minelli 1998); (mspf) – medial spinous processes of ultimate femur, (mspt) – medial spinous processes of ultimate tibia, (vsp) – ventral spinous process of ultimate femur, (t1) – tarsus 1, (up) – ultimate pretarsus, (chl) – chitin-lines, (ptp) – process of trochanteroprefemur.

Holotype:

Puerto Rico, Florida Co., Rio Encantado Cave, 1 (sub?)adult, 29.07.2009, leg. P. Beron (NMNHS).

Locus typicus.

Puerto Rico, Florida Co., Rio Encantado Cave.

Derivatio nominis:

named after my friend and colleague Dr Pavel Stoev who drew my attention to this new species.

Diagnosis.

Tergite 1 with rounded anterior transverse suture and incomplete paramedian sutures. Sternites distinctly margined laterally. Ultimate legs: prefemur with 4, femurwith 3 small spinous processes medially and 1 ventrally; tibia with 2 small spinous processes medially. Tarsus 1 large and clavate (bulbous), clearly differing from the much thinner tarsus 2; the latter consisting of 19–20 articles.

Description.

Length of body ca 17 mm, length of ultimate legs about 9 mm. Color (in ethanol): entire animal uniformly light-yellow with cephalic plate and forcipular segment slightly darker (Fig. 1). Body sparsely pilose; sternites and legs less setose than tergites. PageBreakAntennae composed of 17 articles (Fig. 2), reaching rear edge of tergite 5 when folded backwards; 2.5 basal antennal articles covered by a few long setae, subsequent articles densely pilose. Basal antennal articles somewhatflattened dorso-ventrally. PageBreakHead: cephalic plate visibly longer than wide, with rounded corners and very short paramedian sutures at posterior margin. Second maxillae: as in all other species but dorsal spur on article 2 of the telopodite not recognisable. Pretarsus without spurs, with well-developed dorsal brush. The angle between the longitudinal axes of pretarsus and article 3 of telopodite slightly more than 100° (Fig. 3), which is quite unusual condition in Scolopendromorpha. Forcipular segment: coxosternite without any visible sutures (including thechitin-lines). Anterior margin of coxosternite evidently convex (Fig. 3), divided by a median diastema into two low additionally sclerotised lobes; each lobe bearing a longseta. Trochanteroprefemoral process absent. Tarsungula normal. Tergites: anterior margin of tergite 1 covered by the cephalic plate; tergite 1with a rounded anterior transverse suture and paramedian sutures stretching from the transverse suture to the posterior tergal margin. Tergite 3 with a very characteristic thin oblique sutures bordering the anterior corners of tergite. Tergites 2-22 with complete paramedian sutures, tergites 3-21(22)withlateral longitudinal sutures (Fig. 4). Tergite 23 lacking sutures, its posterior margin convex. Tergite margination virtually absent, only tergite 23 distinctly margined laterally.Tergite 23 much wider rather than long and nearly rectangular in shape; its lateral sides slightly rounded (Fig. 4). All tergites without medial keel; pretergites also missing. Sternites: trapeziform, 2-22 with incomplete (equally shortened from both sides) but with a well expressed median longitudinal sulcus. Sternites 2-21 with definite and complete lateral margination (Fig. 5) through lateral longitudinal sutures (see Remark 2); endosternites absent. Sternite 23 trapeziform, with a few very short (spur-like) setae on lateral sides (Fig. 6), with a straight posterior margin. Legs: prefemur, femur and tibia with a few large setae (Fig. 5); tarsi with more numerous setae of various length and size. Tibia of legs 1–20 with a lateral spur; both, ventral tibial spur and tarsal spur absent. Tarsi of legs 1–21 (Fig. 5) without distinct division between tarsus 1 and 2; pretarsi long, thin and sharply pointed.Pretarsi of legs 1-22 with two thin and long (as long as 1/2 of pretarsus)accessory spines. Coxopleuron (Figs 6, 7):nearly completely pierced with coxal pores of various size – only coxopleural process and a narrow area bordering posterior margin of coxopleuron remaining poreless. Coxopleural process (Figs 6, 7)as long as ultimate sternite, conical, without additional spines. Coxopleural surface without setae.Posterior margin of pleuron of ultimate leg-bearing segment forming avery obtuse angle. Ultimate legs (Fig. 8): slender, ca 9 mm long, width of prefemur ca 0.5 mm.Prefemur triangular in cross-section, with a standard row of 4 ventral spinous processes (Fig. 7), some spurs (strong, spine-like setae of various length) dorso-laterally and more numerous similar spurs dorso-medially (Fig. 4). All four prefemoral ventral spinous processes are of the same size, apically curved and ending in a pointed harpoon-like tip, which is accompanied by a long seta. Femurcylindrical,with 3 small spinous processes medially (Fig. 9) and 1 ventrally in the middle of femur (Fig. 10). Tibia cylindrical, with 2 small spinous processes medially: one close to its base and another at mid length (Figs 9, 10). Both femoral and tibial spinous processes are acPageBreakPageBreakPageBreakcompanied by a single long ventral seta. Tibia practically as long as prefemur or femur. Tarsus well divided into tarsus 1 and tarsus 2 (Fig. 8), former as long as 1/2 of tibia. Tarsus 1 (Figs 8–10) is enlarged and clavate (bulbous); tarsus 2 thin, consisting of 19 (or 20) articles (Fig. 8). In a few places annulation of tarsus 2 is somewhat vague; for example, the very long ultimate article seems to consist of two articles, which are not well divided. Ultimate legs without pretarsus.

Range.

The species is hitherto known only from its type locality.

Habitat and associated fauna.

Being -250 m deep and 16 910 m long Rio Encantado is the deepest and the longest cave system in Puerto Rico. This system lies in the Tertiary limestone area which stretches along the northern coast of the island (Peck 1974). has been collected deep inside the cave, in the aphotoc zone and although apparent troglomorphic traits are lacking it may well represent a troglobite, as its congener from Sistema de Purificacion, Mexico, (Chagas and Shelley 2003). In the cave it co-occurs with amblypigs, spiders, beetles (Dr. P. Beron, pers. comm.). ,sp. n. 1 Habitus 2 Head and anterior segments, ventral view 3 Forcipular segment, ventral view 4 Tergites 22 and 23 and prefemora of ultimate legs, dorsal view; (pt) – pretarsus of second maxilla, (ar3) – article 3 of telopodite of second maxilla, (cxs) – forcipular coxosternite, (am) – anterior margin of coxosternite, (t) – tarsungulum, (ps) – paramedian sutures, (lls) – lateral longitudinal sutures, (ut) – tergite of ultimate leg-bearing segment, (sup) – spurs of ultimate prefemur. ,sp. n. 5 Segments and midbody legs, ventral view 6 Posterior body end, ventral view 7 Left side of ultimate leg-bearing segment and prefemora of ultimate legs, ventro-lateral view 8 Ultimate legs, ventro-lateral view; (mls) – median longitudinal sulcus, (ls) – lateral sutures, (lm) – lateral margination, (s) – setae, (tl) – monoarticulated tarsus of locomotory leg, (us) – sternite of ultimate leg-bearing segment, (cx) – coxopleuron, (cxp) – coxopleural process, (pm) – posterior margin of pleuron of ultimate leg-bearing segment, (vsp) – ventral spinous processes of ultimate prefemur, (p) – prefemur, (f) – femur, (t) – tibia, (t1) – tarsus 1, (t2) – tarsus 2. ,sp. n. 9 Femora, tibiae and tarsi 1 of ultimate legs, dorsal view 10 Femora, tibiae and tarsi 1 of ultimate legs, ventral view; Chamberlin, 1922 11 Forcipular segment, ventral view (after Schileyko and Minelli 1998); Chamberlin, 1921 12 Ultimate legs, dorso-lateral view (after Schileyko and Minelli 1998); (mspf) – medial spinous processes of ultimate femur, (mspt) – medial spinous processes of ultimate tibia, (vsp) – ventral spinous process of ultimate femur, (t1) – tarsus 1, (up) – ultimate pretarsus, (chl) – chitin-lines, (ptp) – process of trochanteroprefemur.

Discussion

1 This species is morphologically close to Chamberlin, 1918 from which it can be readily distinguished by the following traits of the ultimate pair of legs: number of articles of tarsus 2 (19 vs. 9 in ); presence of 4 (vs. 3 in ) spinous processes on femur; presence of 2 (vs. 0 in ) such processes on tibia. 2 Schileyko (2009) wrote that in the family Scolopocryptopidae the lateral sternal sutures are known in , Chamberlin, 1915, Archey, 1923, Chamberlin, 1912 and Shelley & Mercurio, 2005. It should be noted, that Chagas (2011) considered as a junior synonym of . The lateral sternal sutures may be developed in various degrees (from complete to quite short), but only (see fig. 144 in Shelley 2002) and Schileyko, 2009 have sterna with elevated lateral margins. However, in the lateral longitudinal sutures border the complete lateral margination, which seems to be considerably elevated over the surface of sternite. 3 Some groups of scolopendromorphs (the majority of Scolopendrinae, Otostigminae, Scolopocryptopinae and Plutoniumidae) have a well-developed, strongly sclerotized disto-medial projection of the forcipular trochanteroprefemur. Formerly, I used the term “forcipular median tooth” for it, but Bonato et al. (2010) proposed the term “process of trochanteroprefemur”. The Newportiinae either entirely lack this process, or have it only as a small denticle (Fig. 11), similar to some geophilomorphs, for which Bonato et al. (2010) proposed the term ‘distal denticles of trochanteroprefemur’. 4 As for the vague annulation of some articles of ultimate tarsus 2 in , I should mention that there are a few other species of in which this trait is observed, for example Chamberlin, 1957 and ChamPageBreakberlin, 1921 (see REMARKS to and Figure 5c of in Schileyko and Minelli 1998). 5 In some species of legs have one tarsal spur and two (lateral and ventral) tibial spurs, other species have one (lateral) tibial spur only (as ) and in Chamberlin, 1950 spurs are entirely lacking (see p. 290 in Schileyko and Minelli 1998). In some species of (for example in Verhoeff, 1938) lateral tibial spur is situated on an outgrowth of disto-lateral side of the tibia (see Fig. 2a in Schileyko and Minelli 1998). It is also worth mentioning that tibial spurs do not break off easily in as these spurs would do, for example, in . Absence of tibial spurs is another character that separates Ectonocryptopinae from Newportiinae.

Identification key to the species of

One of the main problems for identification of scolopendromorph centipedes is the high number of new species, described in the last decades that are still remaining outside the contemporary identification keys. I suggest that every description of new species in large genera (like ) to be accompanied by the respective update of the available identification key. In cases where the genus includes just a few species, the identification key should be completely re-written. The most recent key to the species of was provided by Schileyko and Minelli (1998). Since then several new species have been described by González-Sponga (1997, 2000) and Chagas and Shelley (2003) from Venezuela and Mexico, respectively. The latter authors have also revived Humbert & Saussure, 1869, although in the same paper they also stated (pp. 13-14): “We … do not think that any conclusion [about the validity of azteca] can be reached”. In 1998 Schileyko and Minelli wrote (p. 291): “Another nominal taxon very similar if not identical to and seems to be Humbert & Saussure, 1869: 158 [cf. Attems, 1930: 275] whose true identity, however, remains to us as doubtful as it was to Attems [1930]”. However, Chagas and Shelley (2003) were absolutely correct when writing (p. 13) that is the third oldest name in (after and ) and in case of synonymy would have priority by 27 years over . Since there is no available characters at the moment to separate these two species I put them together in the following identification key. Both, sp. n. and , are included in the key provided below. With regards to the seventeen new species of described from Venezuela by González-Sponga (1997, 2000), they will be analyzed in a paper dedicated to the scolopendromorph fauna of Venezuela that is currently in progress. sp. 13 Cephalic plate and tergites 1-3, dorsal view (after Schileyko and Minelli 1998, re-drawn); Kraus, 1955 14 Cephalic plate and tergite 1, dorsal view (after Schileyko and Minelli 1998); Chamberlin, 1921 15 Cephalic plate and tergites 1-3, dorsal view (after Schileyko and Minelli 1998); Chamberlin, 1945 16 Cephalic plate and tergite 1, dorsal view (after Chamberlin 1945, re-drawn); (ats) – anterior transverse suture, (ps) – paramedian suture. Schileyko & Minelli, 1998 17 Cephalic plate and tergites 1-3, dorsal view (after Schileyko and Minelli 1998); Kraus, 1955 18 Right ultimate leg, medially (after Schileyko and Minelli 1998); Pocock, 1890 19 Right ultimate leg, ventral view (after Schileyko and Minelli 1998); Chamberlin, 1955 20 Ultimate leg: distal portion of tibia and tarsus, ventral view (after Chamberlin 1955); (ats) – anterior transverse suture, (ps) – paramedian suture, (t) – tibia, (t1) – tarsus 1, (t2) – tarsus 2. Schileyko & Minelli, 1998 21 Right ultimate leg, medially (after Schileyko and Minelli 1998); Chamberlin, 1922 22 Cephalic plate and tergites 1-3, dorsal view (after Chamberlin 1922, re-drawn); (ats) – anterior transverse suture, (ps) – paramedian suture, (t) – tibia, (t1) – tarsus 1, (t2) – tarsus 2.
1Tarsus 2 of ultimate legs clearly divided into distinct articles 2
Tarsus 2 of ultimate legs undivided31
2Ultimate leg with a well-developed (claw-shaped) pretarsus which is as long as, or longer than half of the ultimate article of tarsus 2 (Fig. 12) Newportia unguifer
Ultimate leg without a well-developed pretarsus3
3Tergite 1 without an anterior transverse sutureNewportia sargenti
Tergite 1 with an anterior transverse suture4
4Tergite 1 with a rounded anterior transverse suture and, generally, with paramedian sutures which do not form a “W” just behind the anterior transverse suture; in a few species these sutures are absent or extremely short (Fig. 13) 5
Tergite 1 with an anterior transverse suture in the form of a very obtuse angle and with paramedian sutures forked anteriorly, thus forming a “W” just behind the anterior transverse suture (Fig. 14) 21
5Some pairs of legs, usually 2(4)-(19)20, with tibial spurs6
Tibial spurs missing on all legsNewportia phoretha
6Femur of ultimate legs without spinous processes7
Femur of ultimate legs with spinous processes10
7Tergite 1 with rudimentary paramedian sutures (Fig. 13) or sutures completely lacking Newportia pusilla
Paramedian sutures of tergite 1 half-complete or complete, sometimes shortly interrupted in the middle8
8Coxopleural process extremely short; tergite 1 with poorly developed paramedian sutures (Fig. 15) which cross the anterior transverse suture Newportia diagramma
Coxopleural process normal (Fig. 7); tergite 1 with well-developed paramedian sutures stretching between anterior transverse suture and posterior tergal margin 9
9Tarsus 2 of ultimate legs composed of 19–25 articlesNewportia aureana
Tarsus 2 of ultimate legs composed of 6–7 articlesNewportia longitarsis tropicalis
10Tibiae 2-20 with lateral and ventral spurs11
Tibiae 2-20 with a lateral spur only12
11Femur of ultimate legs with 1(-2) ventral spinous process(es)Newportia cubana
Femur of ultimate legs with 2-3 medial spinous processesNewportia longitarsis virginensis
12Tarsus 2 of ultimate legs composed of 4 articles; tarsus 1 almost as long as the tibiaNewportia dentata
Tarsus 2 of ultimate legs composed of 7-26 articles; tarsus 1 quite shorter than the tibia13
13Tarsus 2 of ultimate legs composed of 26 articles; cephalic plate without paramedian suturesNewportia leptotarsis
Tarsus 2 of ultimate legs composed of 7–20 articles; cephalic plate often with incomplete paramedian sutures14
14Anterior ends of the half-complete paramedian sutures of tergite 1 very shortly bifurcate behind the anterior transverse suture (Fig. 16) Newportia oligopla
Paramedian sutures of tergite 1 from absent to complete, never bifurcated anteriorly15
15Tarsus of ultimate legs uniformly divided, without distinction into tarsus 1 and tarsus 2Newportia adisi
Tarsus of ultimate legs distinctly divided into tarsus 1 and tarsus 216
16Femur of ultimate legs with 3-4 spinous processes17
Femur of ultimate legs with 1-2 spinous processes18
17Femur of ultimate legs with 3 spinous processes, tibia without spinous processes and tarsus 2 composed of 9 articlesNewportia heteropoda
Femur of ultimate legs with 4 spinous processes, tibia with 2 spinous processes (Figs 9, 10) tarsus 2 of 19 articles (Fig. 8) Newportia stoevi sp. n.
18Tergite 1 with complete paramedian sutures which cross the anterior transverse sutureNewportia longitarsis longitarsis
Tergite 1 with incomplete paramedian sutures of various length, from half-complete (Fig. 17) to rudimentary (Fig. 13), running between the posterior tergal margin and the anterior transverse suture; rarely without any trace of paramedian sutures 19
19Cephalic plate with a thin transverse suture which crosses the short paramedian sutures close to the posterior margin of the cephalic plateNewportia longitarsis sylvae
Cephalic plate without any transverse suture20
20Prefemur of ultimate legs with 3 large ventral spinous processesNewportia longitarsis guadeloupensis
Prefemur of ultimate legs with 4 large ventral spinous processesNewportia longitarsis stechowi
21Tarsus 2 of ultimate legs composed of 39–40 articlesNewportia sabina
Tarsus 2 of ultimate legs composed of less than 30 articles22
22Each leg with a tarsal spur; tibia of ultimate legs longer than femur23
Legs without tarsal spurs; tibia of ultimate legs shorter or as long as femur26
23Femur of ultimate legs with 2 ventral spinous processesNewportia morela
Femur of ultimate legs with 3 ventral spinous processes24
24Outer branches of forked paramedian sutures of tergite 1 extending in front of the anterior transverse suture up to the anterior border of this tergiteNewportia spinipes + Newportia azteca
Forked paramedian sutures of tergite 1 ending up in the anterior transverse suture25
25Tarsus 2 of ultimate legs consists of 11–12 articles, prefemur laterally with strong setaeNewportia atoyaca
Tarsus 2 of ultimate legs consists of 5–8 articles, prefemur laterally with small spinesNewportia oriena
26Tarsus of ultimate legs composed of uniform articles (Fig. 18) 27
Tarsus 1 and tarsus 2 of ultimate legs with different shapes (Fig. 19) 29
27Tergite 1 with paramedian sutures in front of the anterior transverse suture (Fig. 14); tibia of ultimate legs cylindrical, tarsus composed of 7–9 articles (Fig. 18) Newportia ignorata
Tergite 1 without paramedian sutures in front of the anterior transverse suture; tibia of ultimate legs distinctly claviform distally (Fig. 20), tarsus composed of ca. 15 articles (Newportia weyrauchi) 28
28Prefemur of ultimate legs with 4 ventral spinous processesNewportia weyrauchi weyrauchi
Prefemur of ultimate legs with 3 ventral spinous processesNewportia weyrauchi thibaudi
29Outer branches of the forked paramedian sutures of tergite 1 crossing the anterior transverse suture (Fig. 14) and ending onto the tergal anterior margin 30
Forked paramedian sutures of tergite 1 ending in the anterior transverse suture Newportia monticola
30Femur of ultimate legs medially with one basal and one distal spinous processes, ventrally without them. Sternites 2-12(15) each with a median longitudinal sulcusNewportia fuhrmanni
Femur of ultimate legs medially with one basal spinous process, ventrally with 1-2 such processes. Sternites 2-19 each with a median longitudinal sulcus Newportia simoni
31Ultimate legs with a well-developed claw-shaped pretarsus (which is as long as the poorly distinct ultimate article of tarsus 2)Newportia amazonica
Ultimate legs normally without claw-shaped pretarsus (if a small ultimate claw is present, then it is less than half as long as the poorly distinct ultimate article of tarsus 2)32
32Tibia of ultimate legs with 3 ventral spinous processes; medial spinous processes of prefemur almost as large as the ventral onesNewportia mexicana
Tibia of ultimate legs without spinous processes, medial spinous processes of prefemur (when present) considerably smaller than the large ventral ones33
33Tergite 1 with rounded anterior transverse suture and with or without paramedian sutures34
Tergite 1 with anterior transverse suture angulated caudad to midline and giving rise to short longitudinal suture, which bifurcate caudally (fig. 1 in Chagas and Shelley 2003) Newportia troglobia
34Tergite 1 without paramedian sutures between its posterior margin and the anterior transverse suture, rarely with very short tracks just behind the anterior transverse suture (Fig. 13) 35
Tergite 1 with complete (more rarely half-complete) paramedian sutures37
35Paramedian sutures of cephalic plate very short. Forcipular coxosternite without median suture. Ultimate sternite without median longitudinal sulcus. Femur of ultimate legs with a row of 2-3 spinous processes36
Paramedian sutures of cephalic plate almost reaching its middle. Forcipular coxosternite with a well-developed median suture. Ultimate sternite with a clear median longitudinal sulcus or depression. Femur of ultimate legs without or with a single very small spinous processNewportia maxima
36Tarsus of ultimate legs uniform, without distinct division into tarsus 1 and 2. Forcipular trochanteroprefemur without processNewportia lasia
Tarsus of ultimate legs distinctly divided into a shorter tarsus 1 and a longer tarsus 2 (Fig. 21). Forcipular trochanteroprefemur with a process Newportia patavina
37Paramedian sutures of tergite 1 not bifurcate38
Paramedian sutures of tergite 1 bifurcateNewportia pelaezi
38 Anterior transverse suture of tergite 1 interrupted between the paramedian sutures (Fig. 22) Newportia divergens
Tergite 1 with a complete anterior transverse suture (Figs 15, 17) 39
39Tarsus of ultimate legs uniformNewportia brevipes
Tarsus 1 of ultimate legs abruptly differing from the tarsus 2 40
40Cephalic plate with a transverse suture crossing the paramedian sutures near the posterior margin (Newportia ernsti) 41
Cephalic plate without transverse suture (Fig. 13) 42
41Prefemur of ultimate legs with 6 (rarely 7) ventral spinous processes. Transverse suture of cephalic plate very distinctNewportia ernsti ernsti
Prefemur of ultimate legs with 5 ventral spinous processes. Cephalic plate: median part of transverse suture between the paramedian sutures often poorly visible Newportia ernsti fossulata
42Paramedian sutures of tergite 1 ending up in the anterior transverse suture; tergite 2 with complete paramedian suturesNewportia bielawskii
Paramedian sutures of tergite 1 complete, crossing the anterior transverse suture; tergite 2 with short paramedian sutures or sutures totally missing43
43Tergite 2 without paramedian sutures (these begin from tergite 5-6 onwards); four basal articles of tarsus 2 of ultimate legs definitely separated from each other (fig. 9 in Chamberlin 1957) Newportia albana
Tergite 2 with shortened paramedian sutures (Fig. 22); all articles of tarsus 2 of ultimate legs not well separated 44
44All legs with a tarsal spur and both lateral and ventral tibial spursNewportia stolli
All legs with a lateral tibial spur onlyNewportia paraensis
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