Redescription of Isotominella geophila Delamare Deboutteville, 1948 from Algeria (Collembola, Entomobryomorpha, Isotomidae), a second world record for an Ivory Coast species

Isotominella geophila Delamare Deboutteville, 1948, from Massif Edough in Northeast Algeria, has been found for the second time and is redescribed. It is separated from all other genera of Isotomidae by the following combination of characters: absence of eyes and pigment, PAO oval, not subdivided, shorter than width of antennal base, dens partially crenulated, dental chaetotaxy with more than six setae (13+4), posterior central S-setae on thoracic tergite II to abdominal tergite IV in p-row, S-seta on abdominal tergite V not thickened and mucro bidentate. This species exhibits sexual dimorphism

A New species of Entomobrya from Northern Algeria (Collembola: Entomobryidae)

Two species of Entomobrya were found among 288 specimens of Collembola sampled in northern Algeria. The identification of the Entomobrya species requires some precautions and consideration of characters beyond color pattern. Preliminary identifications suggested the presence of E. mauretanica Handschin, 1925 (new status) and E. clitellaria Guthrie, 1903, but a detailed examination of the specimens assigned to E. clitellaria showed that a new species was involved which is described here. Entomobrya mauretanica has only been collected once before, was described inadequately, and is redescribed here

Global fine-resolution data on springtail abundance and community structure

Springtails (Collembola) inhabit soils from the Arctic to the Antarctic and comprise an estimated ~32% of all terrestrial arthropods on Earth. Here, we present a global, spatially-explicit database on springtail communities that includes 249,912 occurrences from 44,999 samples and 2,990 sites. These data are mainly raw sample-level records at the species level collected predominantly from private archives of the authors that were quality-controlled and taxonomically-standardised. Despite covering all continents, most of the sample-level data come from the European continent (82.5% of all samples) and represent four habitats: woodlands (57.4%), grasslands (14.0%), agrosystems (13.7%) and scrublands (9.0%). We included sampling by soil layers, and across seasons and years, representing temporal and spatial within-site variation in springtail communities. We also provided data use and sharing guidelines and R code to facilitate the use of the database by other researchers. This data paper describes a static version of the database at the publication date, but the database will be further expanded to include underrepresented regions and linked with trait data.</p

Global fine-resolution data on springtail abundance and community structure

CODE AVAILABILITY : Programming R code is openly available together with the database from Figshare.SUPPLEMENTARY MATERIAL 1 : Template for data collectionSUPPLEMENTARY MATERIAL 2 : Data Descriptor WorksheetSpringtails (Collembola) inhabit soils from the Arctic to the Antarctic and comprise an estimated ~32% of all terrestrial arthropods on Earth. Here, we present a global, spatially-explicit database on springtail communities that includes 249,912 occurrences from 44,999 samples and 2,990 sites. These data are mainly raw sample-level records at the species level collected predominantly from private archives of the authors that were quality-controlled and taxonomically-standardised. Despite covering all continents, most of the sample-level data come from the European continent (82.5% of all samples) and represent four habitats: woodlands (57.4%), grasslands (14.0%), agrosystems (13.7%) and scrublands (9.0%). We included sampling by soil layers, and across seasons and years, representing temporal and spatial within-site variation in springtail communities. We also provided data use and sharing guidelines and R code to facilitate the use of the database by other researchers. This data paper describes a static version of the database at the publication date, but the database will be further expanded to include underrepresented regions and linked with trait data.Open Access funding enabled and organized by Projekt DEAL.http://www.nature.com/sdatahj2024Plant Production and Soil ScienceSDG-15:Life on lan

Une nouvelle espèce de Friesea Dalla Torre, 1895, du massif de l'Edough, nord-Constantinois, Algérie (Collembola, Neanuridae)

A new species of Friesea Dalla Torre, 1895, from the Edough massif , north of Constantine, Algeria (Collembola, Neanuridae). Four species of the genus Friesea are newly recorded for Algeria where only one species was previouly known. One of them, new for science, is described in this paper (Friesea laouina n. sp.).Quatre espèces du genre Friesea sont nouvellement citées pour l'Algérie où une seule espèce était connue jusqu'alors. L'une d'entre elles, nouvelle pour la science, est décrite (Friesea laouina n. sp.).Deharveng Louis, Hamra Kroua Salah. Une nouvelle espèce de Friesea Dalla Torre, 1895, du massif de l'Edough, nord-Constantinois, Algérie (Collembola, Neanuridae). In: Bulletin de la Société entomologique de France, volume 109 (2), juin 2004. pp. 141-143

Une nouvelle espèce de Friesea Dalla Torre, 1895, du massif de l'Edough, nord-Constantinois, Algérie (Collembola, Neanuridae)

A new species of Friesea Dalla Torre, 1895, from the Edough massif , north of Constantine, Algeria (Collembola, Neanuridae). Four species of the genus Friesea are newly recorded for Algeria where only one species was previouly known. One of them, new for science, is described in this paper (Friesea laouina n. sp.).Quatre espèces du genre Friesea sont nouvellement citées pour l'Algérie où une seule espèce était connue jusqu'alors. L'une d'entre elles, nouvelle pour la science, est décrite (Friesea laouina n. sp.).Deharveng Louis, Hamra Kroua Salah. Une nouvelle espèce de Friesea Dalla Torre, 1895, du massif de l'Edough, nord-Constantinois, Algérie (Collembola, Neanuridae). In: Bulletin de la Société entomologique de France, volume 109 (2), juin 2004. pp. 141-143

FIGURE 2 in Redescription of Isotominella geophila Delamare Deboutteville, 1948 from Algeria (Collembola, Entomobryomorpha, Isotomidae), a second world record for an Ivory Coast species

FIGURE 2. Isotominella geophila: A, habitus of a male specimen; B, antenna, ventrolateral view, and part of the head showing the PAO and proximal setae (ms, microsensillum); C, fourth antennal segment (bar: 10 micrometers); D, clypeus and labrum; E, mandibles; F, labial palp; G, maxilla

Edoughnura rara Deharveng, Kroua & Bedos, 2007, sp. nov.

Edoughnura rara sp. nov. Figs 1–5, Tab. 1 Type material. Holotype female in slide, Algeria, wilaya of Annaba, Serraidi, Edough massif, below Fontaine Romaine, 750 m, litter in Quercus canariensis forest (zen oak), 18.i. 2005, Hamra Kroua leg. (sample ALG-HK0501/EDlcz 6). Paratypes: two females in slide in the same sample; one male in slide, ibid, below Fontaine Romaine, 750 m, moss on soil in Quercus canariensis forest (zen oak), 18.i. 2005, Hamra Kroua leg. (sample ALG-HK0501/EDms); one female in slide, ibid, above Fontaine Romaine, 800 m, 22.i. 2001, Hamra Kroua leg. (sample ALG-HK01/ED03). Vi 5 Ve 7 or 9 Labrum 2 / 2,4 Labium 9-10 chaetae,? no x Ant. I-II 7, 12 Ant. III 17 + 5 S Ant. IV or, 8 S, i, 12 mou Postcephalic chaetotaxy Holotype female, one paratype female and one paratype male deposited in the collection of the Museum national d’Histoire naturelle de Paris (France); two paratypes females deposited in the collection of the Laboratoire de Biosystématique et Ecologie des Arthropodes (Constantine, Algeria). Description. Body length: 0.7–0.9 mm. Habitus of a Deutonura, but more stout and with shorter antennae. Colour: very pale, mottled grey-blue. Ocelli 2 + 2, pigmented, subequal, hardly larger than surrounding secondary granules and often difficult to observe. All dorsal tubercles well developed (Fig. 1, Tab. 1), with tertiary granules made of 5–15 rounded secondary granules, but not underlined by well-marked reticulations. Abd.V slightly overlapping Abd.VI in dorsal view. Dorsal ordinary chaetae rather thin, bent, inconspicuously or weakly sheathed, pointed or finely blunt, smooth, sometimes bifurcate; some longer and thicker, laterally and on Abd.V-VI. On Abd.V, Di 2 and Di 3 three times shorter than Di 1. S-chaetae very thin, shorter than the closest macrochaetae. Slight plurichaetosis on head, no plurichaetosis on tergites. S-chaetae formula on half tergites from Th.I to Abd.V: 0, 2 +ms, 2 / 1, 1, 1, 1, 1. Head. S-chaetae of Ant.IV of medium length, thick, slightly bent, with S 1 and S 2 slightly shorter and thinner than others; apical vesicle trilobed. Buccal cone short but not truncated (Fig. 2). Cardo strongly bent in its externo-distal part. Maxilla with two thin appressed lamellae, one distally bidentate and one unidentate, mandible as a long, rather thin, ciliated lamella, with two very thin, cilia-like basal teeth (Fig. 3), turned back into the head. Labium with 4 basal (E,F,G,f), 3 distal (A,C,D) and 2-3 lateral (c,d, and sometimes e) chaetae, with chaetae A as long as C and macrochaeta F shift antero-externally (Fig. 2); x-papillae not seen. Labrum truncated-rounded, with ventral sclerifications narrow; its 2 + 2 distal chaetae long and subequal; 1 + 1 lateral prelabral chaetae present, the two inner ones apparently absent (Fig. 4). Eleven tubercles on head (Fig. 1). Af fused to CL with an area devoid of tertiary granules between C and F. Chaeta E absent. Supernumerary chaetae on the tubercle (Af+CL): two at the level of A, two at the level of O, one uneven at the level of C (sometimes absent), and several on the tubercle (L+So) (Fig. 1). Chaetae Di 1 about 1.5 times longer than Di 2, and De 1 about 2 times longer than De 2. Body and appendages chaetotaxy and tubercles (as in Fig. 1 and Tab. 1). Di tubercles fused on Abd.V, Abd.IV and on Abd.III, separated on Abd.II (not always clearly) and forward. Di 1, Di 2 and Di 3 subequal and arranged in an oblique line on Th.II–III. S-chaetae at level of De 2 on Th.II–III and at level of De 1 on Abd.I– III (Fig. 1). On Abd.V, Di 2 and Di 3 short, subequal, at same level, slightly posterior to the edge of the tubercle. Furcal rest as a weak integument swelling, with 6 chaetae and no distinct microchaetae. Anus as a more or less transversal furrow. Tibiotarsal chaetotaxy 18, 18, 17 (chaeta M absent). Claw untoothed. Etymology. The name of the species refers to its rarity compared to other Neanurinae of the Edough massif, and the uniqueness its morphological characteristics.Published as part of Deharveng, Louis, Kroua, Salah Hamra & Bedos, Anne, 2007, Edoughnura rara n. gen., n. sp., an enigmatic genus of Neanurinae Collembola from the Edough Massif (Algeria), pp. 57-61 in Zootaxa 1652 on pages 58-61, DOI: 10.5281/zenodo.17978

Edoughnura Deharveng, Kroua & Bedos, 2007, gen. nov.

Edoughnura gen. nov. Type species. Edoughnura rara sp. nov. Description. Small size. Light grey-blue pigment present on the body. Two pigmented ocelli on each side of the head. Ordinary dorsal chaetae bent, rather short, moderatly thick, not or hardly sheathed. S 7 not enlarged on Ant.IV. Tertiary granules present on the body. Reticulations inconspicuous or absent. Buccal cone short but not truncated. Labrum formula 2 / 2,4, the 2 + 2 distal chaetae subequal. Maxilla with two thin appressed lamellae, one distally bidentate and one unidentate. Mandible as a long, rather thin lamella ciliated in its distal part, with two very thin basal teeth, cilia-like. All dorsal tubercles developed. Eleven tubercles on head: (Af+CL), 2 Oc, 2 Di, 2 De, 2 DL and 2 (L+So). Tubercles Di fused on the axis from Abd.III to Abd.V. Chaetotaxy of the tubercle (Af + CL) on head with 4 or 5 supernumerary chaetae. Anus as a more or less transversal furrow. Tibiotarsal chaetotaxy 18,18, 17 (chaeta M absent). Claw untoothed. Etymology. The name of the genus refers to the region where it has been collected. Gender: feminine. Discussion. The genus Edoughnura differs from other Neanurini by a number of peculiar features: the morphology of dorsal chaetae, the external shift of chaeta F on the labium (as in Protanura papillata, Deharveng 1983: 17), the strongly modified mandible with long ciliated lamella, the presence of supernumerary chaetae on the central area of head (unique among Neanurini), the linear arrangement of Di chaetae on Th. II- III, the fusion of Di tubercles on Abd. III (as in Monobella cassagnaui Deharveng, 1981) and the anus as a more or less transversal furrow. With this combination of unusual characters, Edoughnura appears very isolated in the tribe Neanurini, with possible remote affinities with Endonura (fusion of tubercles Di on Abd. V combined with separation of tubercles Di and De on head). Its mandible recalls that of Crossodonthina, a genus from eastern Asia, which belongs to the tribe Lobellini and has no close relationships with Edoughnura. It suggests special feeding habits.Published as part of Deharveng, Louis, Kroua, Salah Hamra & Bedos, Anne, 2007, Edoughnura rara n. gen., n. sp., an enigmatic genus of Neanurinae Collembola from the Edough Massif (Algeria), pp. 57-61 in Zootaxa 1652 on page 58, DOI: 10.5281/zenodo.17978

Deutonura zana Deharveng, Zoughailech, Hamra-Kroua & Porco, 2015, sp. nov.

&lt;i&gt;Deutonura zana&lt;/i&gt; sp. nov. &lt;p&gt;Figs 1&ndash;9; Tabs 1 A, B&lt;/p&gt; &lt;p&gt; &lt;b&gt;Type material.&lt;/b&gt; Holotype female and one paratype female on slides. Algeria: Massif of Edough. January 2003, moss on tree, Salah Hamra-Kroua leg. (ALG-HK03/EDIVb).&lt;/p&gt; &lt;p&gt; Six barcoded paratypes (Tab. 1); two skins lost, four skins prepared on slides after barcode extraction (one female, three juveniles). Ibid. April 2009, litter of &lt;i&gt;Quercus canariensis&lt;/i&gt;, Salah Hamra-Kroua leg. (ALG-HK09&ndash;07).&lt;/p&gt; &lt;p&gt; Six barcoded paratypes (Tab. 1); six skins prepared on slides after barcode extraction (two subadult males, one male, three females). Ibid. March 2008, litter of &lt;i&gt;Quercus canariensis&lt;/i&gt;, Salah Hamra-Kroua leg. (ALG-HK08&ndash;06).&lt;/p&gt; &lt;p&gt; One paratype female on slide. Ibid. January 2006, litter of &lt;i&gt;Quercus canariensis&lt;/i&gt;, Salah Hamra-Kroua leg. (ALG-HK0601/2).&lt;/p&gt; &lt;p&gt;Five paratypes on slides (one male, one female, three juveniles). Ibid, near a spring. February 2004, moss on soil, Salah Hamra-Kroua leg. (ALG-HK04/ED2).&lt;/p&gt; &lt;p&gt;Two paratypes on slides (one male, one female). Ibid, near a spring. 6 January 2002, rotten wood, Salah Hamra-Kroua leg. (ALG-HK02/ED2).&lt;/p&gt; &lt;p&gt;Type material deposition. Holotype and nine paratypes (including the six skins of barcoded specimens from ALG-HK08&ndash;06) in the Mus&eacute;um National d'Histoire Naturelle (Paris, France); ten paratypes (including the four skins of barcoded specimens from ALG-HK09&ndash;07) in the Laboratoire de Biosyst&eacute;matique et Ecologie des Arthropodes (Universit&eacute; Constantine 1, Algeria).&lt;/p&gt; &lt;p&gt; &lt;b&gt;Non-type material.&lt;/b&gt; Specimens of Collo massif West of Edough massif, the second area where &lt;i&gt;D. zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; occurs, are morphologically identical to those of Edough. They are however not considered as paratypes because they display a significant genetic divergence with specimens of Edough (see &ldquo;barcode characterization&rdquo; below for discussion &lt;b&gt;).&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Six barcoded specimens (Tab. 1); one skin lost, five skins prepared on slides after barcode extraction (one male, three females, one juvenile) and deposited as vouchers in MNHN. Algeria: Massif of Collo, Azakor and Oueldja, March 2011, Berlese extraction, Salah Hamra-Kroua leg. (ALG-HK11&ndash;03).&lt;/p&gt; &lt;p&gt; Two specimens on slides (one female, one juvenile). Ibid, Zitouna, 24.04.2007, litter of &lt;i&gt;Quercus suber&lt;/i&gt;, Salah Hamra-Kroua leg. (ALG-HK07-C1).&lt;/p&gt; &lt;p&gt;Three specimens on slide (two females, one subadult male). Ibid, Khnak Mayoun, 15.02.2013, decaying wood, Abdelmalek Zoughailech leg. (ALG-ZA13&ndash;04).&lt;/p&gt; &lt;p&gt; &lt;b&gt;Etymology.&lt;/b&gt; The species name &lt;i&gt;zana&lt;/i&gt; refers to zan oak (or zeen oak), a traditional arabic vernacular name of &lt;i&gt;Quercus canariensis&lt;/i&gt; Pomel, which constitutes the dominant tree of the forest where &lt;i&gt;Deutonura zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; occurs.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Description.&lt;/b&gt; Length: 1.3&ndash;1.4 mm. Colour: blue. Habitus usual for the genus. Abd. VI well visible from above, weak cryptopygy (Fig. 1). All tubercles well developed, indicated by reticulations and tertiary granules without or on very low papillae (except on the posterior part of tubercle Di of Abd. V), but with strong secondary granules. All dorsal chaetae integrated in tubercles, except D on head which is free (Figs 2, 5). Dorsal ordinary chaetae of four types: long macrochaetae, short macrochaetae and, only on head, mesochaetae and microchaetae. Long macrochaetae long, robust, thick, finely rugose, sheathed, rounded (Fig. 7) to abruptly narrowed and tapering apically; the most lateral ones pointed apically and not sheathed. Short macrochaetae similar to long macrochaetae, but shorter. Mesochaetae and microchaetae thin and acuminate, short, only present on the cephalic tubercles Oc and (L+So). S chaetae of tergites thin and long but much shorter than neighboring long macrochaetae; on Abd. V, Schaeta less than half the nearby macrochaeta. Pseudopores morphologically similar to muscular insertion areas, but with minute perforation-like dots. Pseudopore formula complete: one ventrally on each antennal basis; 1,1/1,1,1,1 from Th. II to Abd. IV by half-tergite, located antero-internally to tubercle De; one uneven posterior on Abd. II sternite; 1+1 posterior on Abd. III sternite; one uneven anterior on Abd. V sternite. Distribution of muscular insertions on tergites and sternites tentatively given on Figs 2 and 8 (a few may have been overlooked). They form a symmetrical pattern with clear partial serial homologies from Th. II to Abd. IV.&lt;/p&gt; &lt;p&gt;Antennae usual for the genus with S-chaetae long, thickened and subequal; chaeta d4 of Ant. III absent; apical vesicle of Ant. IV trilobed (Fig. 3). Mouthparts reduced, mandible thin and tridentate, maxilla styliform. Buccal cone pointed, moderately long: labrum truncated, with ventro-distal sclerification not ogival, its distal edge with many microdenticles (Fig. 4). Eyes black, 2+2.&lt;/p&gt; &lt;p&gt;Chaetotaxy and tubercle arrangement summarised in Figs 2, 8 and Tab. 2. Elementary tubercles DE and EE absent on the cephalic tubercle Af; no granular plate between A and B; a single elementary tubercle between chaetae A (Fig. 5). On Abd. V, Di1 is a thickened, long, bent macrochaeta, 1.5 to 1.8 as long as Di2. Chaeta Di3 at most 4.2 times shorter (in holotype) than Di1, usually much shorter or absent (Fig. 6). Leg chaetotaxy summarised in Tab. 2. No tooth on claw; tibiotarsus with chaeta M present, ventral chaetae B4 and B5 moderately elongate (Fig. 9). Male without modified chaetae ventrally.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Discussion.&lt;/b&gt; &lt;i&gt;Deutonura zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; is a species of the &lt;i&gt;phlegraea&lt;/i&gt; group the most speciose group of the genus &lt;i&gt;Deutonura&lt;/i&gt;, according to the following combination of characters (modified from Deharveng 1982): chaeta E on head located in the antenno-frontal tubercle, dorso-lateral tubercle on head triangular with an antero-internal elementary tubercle reaching the muscular insertion between Af and ocular plates, cryptopygy moderate, never complete.&lt;/p&gt; &lt;p&gt; Within the &lt;i&gt;phlegraea&lt;/i&gt; group, &lt;i&gt;D. zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; is similar to &lt;i&gt;D. deficiens meridionalis&lt;/i&gt; Deharveng, 1979 and to &lt;i&gt;D. luberonensis&lt;/i&gt; Deharveng, 1982 by the following combination of characters: 2+2 ocelli; Af and CL tubercles not fused on head; elementary tubercles DE and EE not differentiated in Af, which has no granular area devoid of elementary tubercle between chaetae A and B; DL3 present on head; one chaeta Di on Th. I; chaeta De3 absent on tubercle De of Th. II; Abd. VI visible in dorsal view; chaeta Di2 longer than Di3 on Abd. V. The new species differs from &lt;i&gt;D. deficiens meridionalis&lt;/i&gt; by the presence of a chaeta O on head. From &lt;i&gt;D. luberonensis&lt;/i&gt;, it differs by the separation of Di and De tubercles on Th. I.&lt;/p&gt; &lt;p&gt;A. Cephalic chaetotaxy.&lt;/p&gt; &lt;p&gt;Chaetal group Tubercle Number of chaetae Type of chaetae Name of chaetae CL + 4 ML F&lt;/p&gt; &lt;p&gt;Mc G&lt;/p&gt; &lt;p&gt;Af + 11 ML B&lt;/p&gt; &lt;p&gt;Mc A,C,D,E,O Oc + 3 ML OCm&lt;/p&gt; &lt;p&gt;McorML OCp&lt;/p&gt; &lt;p&gt;mi OCa&lt;/p&gt; &lt;p&gt;Di + De + 4 ML Di1,De1 Mc Di2,De2 DL + 6 ML DL1,DL5&lt;/p&gt; &lt;p&gt;Mc DL2,DL3,DL4,DL6&lt;/p&gt; &lt;p&gt;L + So + 8 or 9 ML So1,L1,L4 Mc L2&lt;/p&gt; &lt;p&gt;me So 3 to 6 mi L3&lt;/p&gt; &lt;p&gt;Vi: 6&lt;/p&gt; &lt;p&gt;Ve: 8 or 9&lt;/p&gt; &lt;p&gt;Labrum: 2/2,4 Labium: 11, 0x Ant. I,II: 7,12 Ant. III: 17+5s Ant. IV: 12 mou+or+i+8s B. Postcephalic chaetotaxy (see Figs 2 and 8).&lt;/p&gt; &lt;p&gt; As usual among Neanurini, &lt;i&gt;D. zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; exhibits a small proportion of asymmetrical or abnormal specimens; on Abd. V, chaeta Di3 was a short mac in 5 specimens, a mic in 6 specimens and was not detected in 5 juvenile specimens.&lt;/p&gt; &lt;p&gt; The distribution of muscular insertions on tergites and sternites is tentatively given for &lt;i&gt;D. zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; on Figs 2 and 8, with uncertainties regarding mostly lateral parts of head and body. Muscular insertion pattern has previously not been used in taxonomy, but is figured in the literature by Cassagnau (1990, 1993) for several Paleonurini. In particular, the drawings given for head, tergites and sternites of &lt;i&gt;Nepalimeria dal&lt;/i&gt; Cassagnau, 1993 in the original description suggest both homologies and important differences in the distribution of these muscular insertions when compared to &lt;i&gt;Deutonura zana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt; This observation suggests that the distribution of muscular insertions on the body may provide additional specific characters when further investigated.&lt;/p&gt;Published as part of &lt;i&gt;Deharveng, Louis, Zoughailech, Abdelmalek, Hamra-Kroua, Salah &amp; Porco, David, 2015, A new species of Deutonura (Collembola: Neanuridae: Neanurinae) from north-eastern Algeria, and characterisation of two intraspecific lineages by their barcodes, pp. 281-290 in Zootaxa 3920 (2)&lt;/i&gt; on pages 282-288, DOI: 10.11646/zootaxa.3920.2.4, &lt;a href="http://zenodo.org/record/241088"&gt;http://zenodo.org/record/241088&lt;/a&gt