identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
2943C59E1D655DAA913C218785B2B626.text	2943C59E1D655DAA913C218785B2B626.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis dobbsi (Eaton 1912)	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis dobbsi (Eaton, 1912) Figures 5, 6 </p>
            <p> Oligoneuria dobbsi Eaton, 1912: 243, fig. 1 (female imago). </p>
            <p> Oligoneuriella dobbsi : Ulmer, 1924: 32. </p>
            <p> Oligoneuria sp.:  Vayssière , 1936: 130 (nymph). </p>
            <p> Oligoneuriopsis dobbsi : Kimmins, 1960: 276, figs 9, 10 (female and male imagos). </p>
            <p> Oligoneuriopsis grandaeva (  Navás , 1936: 125, fig. 21) (female imago). </p>
            <p>Material examined.</p>
            <p>Kenya • 28N; Mount Elgon, Teremi upstream; 0.8973°N, 34.5973°E; alt. 2456 m a.s.l.; 13 Oct. 2019; W. Graf leg. • 23N; Mount Elgon, Teremi; 0.9094°N, 34.5994°E; alt. 2407 m a.s.l.; 13 Oct. 2019; W. Graf leg. • 13N; Mount Elgon, Kimurio upstream; 0.8913°N, 34.5892°E, alt. 2239 m a.s.l.; 11 Oct. 2019; W. Graf leg. • 46N (among them 1N - GBIFCH00890747 - sequenced); Mount Elgon, Kimurio tributary 2; 0.8956°N, 34.5878°E; alt. 2347 m a.s.l.; 8 Nov. 2019; W. Graf leg. • 15N; Mount Elgon, Kibisi upstream; 0.9028°N, 34.6175°E; alt. 2298 m a.s.l.; 9 Nov. 2019; W. Graf leg. • 8N; Mount Elgon, Kapkateny upstream; 0.8959°N, 34.5990°E; alt. 2293 m a.s.l.; 11 Oct. 2019; W. Graf leg. • 7N; Mount Elgon, Kapkateny midstream; 0.8325°N, 34.6234°E; alt. 1896 m a.s.l.; 12 Oct. 2019; W. Graf leg. • 2N; Mount Elgon, Kapkateny downstream; 0.8144°N, 34.6243°E; alt. 1660 m a.s.l.; 14 Oct. 2019; W. Graf leg.; all MZL.</p>
            <p>Male imago.</p>
            <p> As redescribed by Kimmins (1960), with the following complement extracted from mature male nymphs: penis lobes with characteristic sclerotized proximal process ending in a simple projection; apex of the lateral longitudinal lobe of penis in a small club-shaped sclerite ca. 1.5  × larger than the lateral lobe (Fig. 5B). </p>
            <p>Nymph.</p>
            <p>Lengths. Body up to 17 mm and 25 mm in male and female nymphs respectively; cerci (and caudal filament) up to 10 mm and 11 mm in male and female nymphs, respectively.</p>
            <p> General colouration medium to dark brown, in general darker in mature nymphs than in immature ones (Fig. 6A). Head dark brown, with four lighter maculations between the compound eyes, and a black marking present on the frons between the ocelli; generally also with a rounded light maculation between antennae. Ventrally, head a uniform light brown colour. Gills at base of maxillae forming a  “beard” ventrally at base of head, much paler in colour relative to head capsule (Fig. 6B). Pro- and mesonotum dark brown, with lighter maculae laterally and medially. Legs light to medium brown, femoro-tibial articulation with a blackish spot. Femur and tibia of foreleg shorter than those of mid or hind leg, fore tibia longer than fore femur; on mid- and hind legs, femora and tibiae subequal in length. Setae on the outer margin of mid and hind femora well developed, slightly decreasing in size and reaching the apex (Fig. 5A). Tibiae and tarsi with long, even fringe of setae along entire dorsal margin. Abdominal tergites uniformly dark brown, each with a pair of light spots in the middle, except tergite X which bears four light spots in proximal part. Sternites medium brown, laterally dark brown, with two small pale median markings, especially visible on sternites IV to VIII. Dense patch of posteriorly orientated setae ventromedially moderately developed on abdominal sternite II, well-developed on sternites III-V, absent from other segments. Gills III-VII almost subequal in size, more than  ¾ of the corresponding segment, gill II smaller, ca. 1/2 the size. On all gills except for gill I, fibrillae shorter than lamella length. Lamella of gill I a little bit shorter than the length of the fibrillar portion. Lamellae II-VII with long and thin setae on their distal inner margin. Posterolateral spines of the abdomen absent of segments I and II, then increasing in size from segment III to IX, those of this last one being ca.  ¼ the length of the segment. </p>
            <p>Cerci uniformly medium brown, caudal filament paler brown towards apex.</p>
            <p>Affinities.</p>
            <p> Oligoneuriopsis dobbsi male imago seems to be closely related to  O. lawrencei from which it differs by the presence of crossveins in the proximal part of the subcostal area (see Kimmins 1960, fig. 9), as well as by the shape of the proximal process of the penis sclerite which is shorter and less pointed than in  O. lawrencei . The supposed nymph of  O. dobbsi presents also similarities with the one of  O. lawrencei , but differs in several respects, namely, the absence of a slight carina on the head, the general colouration of the body, the size of gill II, smaller than the following ones in  O. dobbsi , whereas subequal to the following ones in  O. lawrencei , the patch of setae on sternites (II) III-V in  O. dobbsi compared to sternites II-IV (V-VI) in  O. lawrencei , and finally the size of gill I lamella, much shorter in the latter than in  O. dobbsi . </p>
            <p>Remarks.</p>
            <p> The association of the nymphs from Mount Elgon with the adults described by Eaton (1912) as  Oligoneuriopsis dobbsi is putative at the moment, because we have no rearing of the nymphs and no COI sequences from  Eaton’s material. However, we think this association is realistic, for the following reasons. First, male genitalia extracted from a mature nymph are compatible with those drawn by Kimmins (1960), especially the proximal process which is thick and shorter than in the other species, and the apex of the lateral longitudinal lobe of penis which is slightly clavate distally. Secondly, localities for the nymphs and adults are only distant from ca. 100 km, whereas no other  Oligoneuriopsis populations are known in a radius of thousands of kilometres. Additional nymphal material has been collected by Laban Njoroge, National Museums of Kenya, Nairobi, from the Aberdare range of mountains in Central Kenya and one specimen from Mount Kenya. Images of these nymphs correspond completely with the nymphs of  O. dobbsi described here. The Aberdare range is ca. 200 km east of the type locality, Kericho, while Mount Elgon is around 150 km north. It is reasonable to assume that a single species is represented in this area. </p>
            <p>Known distribution.</p>
            <p>Kenya.</p>
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	https://treatment.plazi.org/id/2943C59E1D655DAA913C218785B2B626	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
FF66993ACFCC5DF0B63FA255E3C79DA8.text	FF66993ACFCC5DF0B63FA255E3C79DA8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis elisabethae Agnew 1973	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis elisabethae Agnew, 1973 Figure 8 </p>
            <p> Oligoneuriopsis elisabethae Agnew, 1973: 118, fig. 1C (nymph). </p>
            <p>Material examined.</p>
            <p>Lesotho • 4N; Tsoelikana River; 29.9200°S, 29.0925°E; alt. 2247 m a.s.l.; 21 Jan. 1986; K. Meyer; AMGS; LES 38U • South Africa • 4N; KwaZulu-Natal, Umkomozana River, Sani Pass; 29.5842°S, 29.2883°E; alt. 2870 m a.s.l.; 14 Jan. 2011; T.A. Bellingan; AMGS; GEN 1978C.</p>
            <p>Comments.</p>
            <p> As with  O. jessicae , the material examined by Agnew has been lost. This includes VAL 606G Klip River, Vrede-Volksrust Rd. Bridge 1959/01/14 27.35806°S, 29.35000°E, Free State Province, and VAL 1061B, VAL 1062A. Klein Vaal R., at Goedehoop Farm 1960/03/22 26.8194°S, 30.1333°E, Mpumalanga Province, F.M. Chutter leg. As the material examined is from a different catchment to the type material, no neotype has been designated. </p>
            <p>Male and female imagos.</p>
            <p>Unknown.</p>
            <p>Nymph.</p>
            <p> Lengths. Body up to 16.5 mm (Agnew 1973), sex-based size differences of nymphs not recorded as none of the available material is fully mature. Cerci up to 8.1 mm, caudal filament 3.3 mm. General colouration light brown (Fig. 8A). Head (Fig. 8A) light brown, with darker brown marking between bases of antennae and ocelli and a grey-brown maculation between antennae; carina on frons slightly developed. Ventrally, head a uniform light brown colour; gills at base of maxillae forming a  “beard” ventrally at base of head, much paler in colour relative to head capsule (Fig. 8B). Pro and mesonotum pale brown, with darker maculae laterally. Legs light brown, femoro-tibial articulation with a blackish spot. Femur and tibia of foreleg shorter than those of mid or hind leg; femora and tibiae of mid and hid legs of approximately equal length. Setae on the outer margin of mid and hind femora well developed, evenly distributed along length of margin; mid and hind tibiae and tarsi with well-developed fringe of even setae along the outer margin. Middle and hind legs with basal area of coxae and trochanter, and entire surface of femora covered with small, scattered, dark brown spine-like setae, extending also along ventral margins of tibiae and tarsi, as well as interspersed amongst the fringe of setae along the dorsal margins. </p>
            <p>Abdominal tergites uniformly pale brown, no distinctive patterns except for paired pale cream-coloured markings forming a V-shaped pattern on last three abdominal segments in some specimens (Fig. 8A). Sternites uniform pale brown, with no distinctive markings (Fig. 8B). Dense patch of posteriorly orientated setae ventromedially moderately developed on abdominal sternite II, well-developed on sternites III-V, absent from other segments. Gills paler in colour than abdomen, gill I ventrally orientated, lamella less than one third the length of the fibrillar portion, gills II-VII with rounded lamella, filaments shorter than the corresponding lamella, lamella shorter than half the length of the corresponding segment. Lamellae II-VII with long and thin setae on their distal inner margin. Posterolateral spines of the abdomen of similar size on each segment, each with the tip a darker brown. Cerci uniformly medium brown, caudal filament paler brown towards apex, less than half the length of cerci.</p>
            <p>Affinities.</p>
            <p> Nymphs of  O. elisabethae are less flattened compared to  O. lawrencei , and have the shortest gills relative to the abdominal tergite length of the three South African species, at ca. 1/3 of the length of the tergites. Head similar in shape to  O. jessicae but notably different to  O. lawrencei , which is widest medially. Lateral abdominal spines are well developed; dorsal abdominal spines as seen in  O. jessicae are absent in  O. elisabethae. Nymphs of  O. elisabethae also differ from those of  O. skhounate ,  O. dobbsi ,  O. orontensis and  O. villosus by the reduction of the caudal filament. </p>
            <p>Habitat preference.</p>
            <p>Found in cobble, pebble and gravel substrate in swift current.</p>
            <p>Known distribution.</p>
            <p>Lesotho; South Africa: Free State and Mpumalanga Provinces.</p>
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	https://treatment.plazi.org/id/FF66993ACFCC5DF0B63FA255E3C79DA8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
CDC3376233AA5704807753FD37EC01F6.text	CDC3376233AA5704807753FD37EC01F6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis jessicae Agnew 1973	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis jessicae Agnew, 1973 Figure 7 </p>
            <p> Oligoneuriopsis jessicae Agnew, 1973: 116, fig. 1A, B (nymph). </p>
            <p>Material examined.</p>
            <p>Eswatini (former Swaziland) • 14N; Malolotja stream, Nkomati River system; 26.1167°S, 31.1144°E; alt. 1227 m a.s.l.; 3 Mar. 2003; R. Bills leg.; AMGS; GEN 1733E • 7N; Jubukweni stream near Mbuluzi, Nkomati River system; 26.2028°S, 31.1944°E; alt. 1044 m a.s.l.; 29 Mar. 2003; R. Bills leg.; AMGS; GEN 1734B • 4N; Lubuyane stream near Mnyokane, Nkomati River system; 26.1572°S, 31.2081°E; alt. 1435 m a.s.l.; 4 Apr. 2003; R. Bills leg.; AMGS; GEN 1738B.</p>
            <p>Comments.</p>
            <p> Agnew (1973) examined material from the National Institute for Water Research (NIWR), Pretoria, and stated it would be housed in the Transvaal Museum (now known as Ditsong Museum). However, Agnew (pers. comm., 1983) indicated that when he moved from the university where he had been based, the technicians in his former laboratory discarded all of the material that he had left in his office, including all of the  Oligoneuriidae material he had examined. Examination of mayfly material in Ditsong Museum (February 2019), and discussions with the late Curator Dr Martin Kruger† (pers. comm., 22 February 2019) confirmed that this material was not in this museum. As no material has since been collected from or near to the type locality (Queen River, 35 km from Barberton, 25.8200°S, 30.8100°E), no neotype has been designated. </p>
            <p>Male and female imagos.</p>
            <p>Unknown.</p>
            <p>Nymph.</p>
            <p> Lengths. Body up to 20 mm and 22 mm in male and female nymphs respectively; cerci (and caudal filament) up to 14 mm (4.5 mm) and 15.8 mm (6.9 mm) in male and female nymphs respectively. General colouration pale to hazelnut brown, with small, paired paler spots in the middle of each tergum of mature nymphs in some individuals; head pale to dark brown, without markings, darker between eyes, becoming paler brown towards distal margin of head (Fig. 7A). Ventrally, head chestnut brown, gills at base of maxillae forming a pale cream coloured  “beard” ventrally at base of head. Pro- and mesonotum dark brown, with pale brown marking on mesonotum, forming a distinct M-shape in mature nymphs. Legs light brown, femoro-tibial articulation darker; setae of forelegs light brown, same colour as the legs. Femur and tibia of foreleg shorter than those of mid or hind leg; in all cases, femora longer than tibiae. Coxal-femoral articulation of mid and hind legs with dark brown stripe ventrally. Setae on the outer margin of mid and hind femora well developed, tapering off slightly in length towards the apex, scattered spatulate setae over entire surface but more concentrated along margins; mid and hind tibae and tarsi with strong fringe of fine, even setae along the outer margin. Distal end of tibiae of mid legs with three stout spines on inner side. </p>
            <p>Abdominal tergites darker than sternites, no distinctive markings except for dorsal paired paler brown spots on each side of the midline of the tergites in mature specimens; sharply pointed dorsal tubercles present on tergites I-VII, gradually decreasing in size posteriorly (Fig. 7A); sternites uniform pale brown, with no markings. Dense patch of posteriorly orientated setae ventromedially on abdominal segments II-V, much reduced patch on segment VI. Gills II-VII almost subequal in size, gill I smaller. On all gills except for gill I, fibrillae slightly shorter than lamella length. Lamella of gill I less than half the length of the fibrillar portion. Lamellae II-VII with long and thin setae on their distal inner margin. Posterolateral spines of the abdomen increasing in size posteriorly. Cerci and caudal filament uniformly medium brown.</p>
            <p>Whole nymph (dorsal aspect) and gills as illustrated by Agnew (1980) and Fig. 7A. Lateral view of anterior of nymph (Fig. 7B), shows dorsal abdominal spines in profile.</p>
            <p>Affinities.</p>
            <p> Nymphs of  O. jessicae mainly differ from those of  O. lawrencei by the presence of sharply pointed dorsal tubercles on tergites I-VII. The dorsal setae along the hind femur are long in  O. lawrencei ,  O. dobbsi and  O. elisabethae , extending to the apex of the femur, while in  O. jessicae the setae are shorter and taper off, not reaching the apex. Gills in  O. jessicae are shorter than the half length of the corresponding tergite, as in  O. elisabethae , while in  O. lawrencei , the gills reach approximately half length of the corresponding tergite, even longer in  O. dobbsi . Adult material is needed for comparison with other species. </p>
            <p>Habitat preference.</p>
            <p>Moss-covered stones in current. Nymphs mature in April (autumn).</p>
            <p>Known distribution.</p>
            <p>Eswatini; South Africa: Mpumalanga near Barberton.</p>
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	https://treatment.plazi.org/id/CDC3376233AA5704807753FD37EC01F6	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
BBCCDF446EE95FB48339751CFB7FB531.text	BBCCDF446EE95FB48339751CFB7FB531.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis lawrencei Crass 1947	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis lawrencei Crass, 1947 Figures 2, 3, 4, 14D, 15D </p>
            <p> Oligoneuriopsis lawrencei Crass, 1947: 53, figs 3, 4. </p>
            <p>Material examined.</p>
            <p>Neotype: South Africa • 1N; Eastern Cape Province, Tributary of Tyume River, below Tor Doone, Hogsback; 32.5778°S, 26.9347°E; alt. 1445 m a.s.l.; 29 Feb. 1992; F.C. de Moor leg.; AMGS; GEN 1097A; H.M. Barber-James design., 2020. This specimen was chosen because it comes from one of Crass (1947) 's original localities.</p>
            <p>Other material: South Africa • 1N; Eastern Cape Province, Tsitsa River, at "The Falls"; 31.0214°S, 28.4819°E; alt. 1140 m a.s.l.; 26 Mar. 1991; F.C. de Moor &amp; H.M. Barber leg.; AMGS; ECR 92AE • 6N; same locality; 28 Mar. 1993; F.C. de Moor &amp; H.M. Barber-James &amp; K. Martens leg.; AMGS; ECR 134A • 12N; Eastern Cape Province, Nqancule River, at Waterval; 31.3672°S, 28.2167°E; alt. 1220 m a.s.l.; 24 Mar. 1991; F.C. de Moor &amp; H.M. Barber leg.; AMGS; ECR 86A • 6N; Eastern Cape Province, Nqancule River, at Albany; 31.3486°S, 28.2153°E; alt. 1240 m a.s.l.; 5 Mar. 1991; F.C. de Moor &amp; H.M. Barber leg.; AMGS; ECR 88A • 1N; Eastern Cape Province, Kettle Spout waterfall, Tyume River tributary, Hogsback; 32.5500°S, 26.9500°E; alt. 1835 m a.sl.; 19 May 2007; F.C. de Moor and N. Phaliso leg.; AMGS; GEN 1845A • 3♀, 4♂, 1N; KwaZulu-Natal, Klein Mooi River, at Durleigh Farm; 29.2283°S, 29.8997°E; alt. 1392 m a.s.l.; 15 Mar. 1995; C. Dickens; AMGS; MOI 29BS • 3♀ 4♂; same locality; 3 Apr. 1995; F.C. de Moor leg; AMGS; MOI 35B.</p>
            <p>Male imago.</p>
            <p>Lengths. Body: up to 14.8 mm; forewing: up to 14.9 mm; cerci: up to 17.0 mm; caudal filament: up to 12.8 mm.</p>
            <p>Vertex light brown, frontoclypeus pale cream, broadly rounded apically, compound eyes black, base of ocelli black, ocelli whitish, antennae with scape and pedicel pale cream, first segment and flagellum light brown. Pronotum light brown, margins suffused with dark brown pigmentation. Pterothorax light brown, with pale cream-coloured unsclerotized line between meso and metanotal plate. Mesoscutellar filaments present. Forelegs shorter than mid or hind legs, with outer margin of femora, tibiae and tarsi dark brown, otherwise uniform pale brown colour; mid- and hindlegs cream to light brown, no distinct markings. All three pairs of legs appear to be functional. Tarsal claws paired, blunt. Wings (Fig. 2), when folded, light brown, almost whitish when unfolded. Forewing typical of the genus, with five groups of veins: Sc+RA, RSa+iRS, RSp+MA1, MA2+MP1, and a forked MP2+CuA - CuP vein. Subcostal field with numerous transversal veins, those issued from RA not reaching iRS in the distal forth of the length, those between iRS and MA1 only present in the proximal half.</p>
            <p> Abdominal segments uniformly creamish, without distinct patterns, except tergites VII, IX, and X light brown; lateral margins with spine-shaped extensions from segment III to IX, of increasing length towards the posterior. Gonostyli whitish to grey, cerci whitish. Gonostyli 4-segmented, the basal one ca. 3  × the length of segments 2 to 4 combined. Penis lobes almost triangular, with characteristic sclerotized proximal process ending in a simple projection; apex of the lateral longitudinal lobe of penis in a small club-shaped sclerite (Fig. 3). Cerci with whorls of long setae at each junction (not figured). </p>
            <p>Female subimago.</p>
            <p>Lengths. Body: up to 17 mm; forewing: up to 18.8 mm; cerci: up to 7 mm; caudal filament: up to 4.5 mm. Colouration as in the male; tibiae and tarsi of all legs appear to be functional. Cerci light to medium brown. Posterior margin of sternite IX deeply concave and rounded.</p>
            <p>Nymph.</p>
            <p> Lengths. Body up to 15 mm and 18.5 mm in male and female nymphs respectively; cerci (and caudal filament) up to 9.2 mm (4.0 mm) and 10.1 mm (3.5 mm) in male and female nymphs respectively. General colouration light to medium yellow-brown (Fig. 4A), with dark brown dorso-medial markings, better developed in mature male nymphs than in immatures or females. Head (Fig. 4B) medium brown, with maculation between the compound eyes. Ventrally, head a uniform pale cream colour. Gills at base of maxillae forming a  “beard” ventrally at base of head, of similar colour to head in Hogsback specimens, orientated in one plane, parallel to length of body. Pro and mesonotum medium brown, with pale cream-coloured maculae. Legs light brown, femoro-tibial articulation darker, setae of forelegs noticeably darker brown than the legs. Femur and tibia of foreleg shorter than those of mid or hind leg, in all cases, femora and tibiae subequal in length. Setae on the outer margin of mid and hind femora well developed, slightly decreasing in size and reaching the apex (Fig. 14D). Tibiae and tarsi with long, even fringe of setae along entire dorsal margin, interspersed with occasional short spine-like setae. Abdominal tergites uniformly medium brown, each with darker brown marking medially; sternites uniform pale brown, with no markings. Dense patch of posteriorly orientated setae ventromedially on abdominal sternites II-IV, much reduced patch on segments V, further reduced on VI. Gills II-VII almost subequal in size, gill I smaller. On all gills except for gill I, fibrillae shorter than lamella length. Lamella of gill I less than half the length of the fibrillar portion. Lamellae II-VII with long and thin setae on their distal inner margin (Fig. 15D). Posterolateral spines of the abdomen increasing in size posteriorly. Whole nymph (dorsal aspect) and gills as illustrated by Agnew (1980). Cerci uniformly medium brown, caudal filament paler brown. </p>
            <p>Intraspecific variation.</p>
            <p>Specimens from KwaZulu-Natal are darker brown in colour than specimens with more southerly distribution, and first three abdominal segments darker brown in colour dorsally than remaining segments; faint paired median spots visible on the last five abdominal tergites in some KwaZulu-Natal nymphs. The head also possesses a dark brown marking present on the frons between the ocelli, and maxillary gills are much paler in colour relative to head capsule in KwaZulu-Natal specimens.</p>
            <p>Affinities.</p>
            <p> Winged stages were collected from the same locality as the nymphs in one instance, allowing association of the life stages. Imagos were seldom flying at the times of collection. Nymphs of  O. lawrencei have a broadly rounded fronto-clypeal region, which easily distinguishes them from  O. jessicae and  O. elisabethae , both of which are more pointed in shape. Head very slightly carinate, less so than in  O. elisabethae . Note that this is unlike the strong carination seen in  Elassoneuria . </p>
            <p>Habitat preference.</p>
            <p>Found under large boulders (400-500 mm diameter) in swift current, often in rivers with bedrock substrate.</p>
            <p>Known distribution.</p>
            <p>South Africa.</p>
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	https://treatment.plazi.org/id/BBCCDF446EE95FB48339751CFB7FB531	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
71EEB0A8E51957C49176844730E66534.text	71EEB0A8E51957C49176844730E66534.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis orontensis (Koch 1980) Barber-James & Zrelli & Yanai & Sartori 2020	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis orontensis (Koch, 1980) comb. nov. Figures 9B, 10B, 11D-F, 12B, 14F </p>
            <p> Oligoneuriella orontensis Koch, 1980: 154, figs 1-4 (nymph). </p>
            <p>Material examined.</p>
            <p> Israel • 1N; Jordan River, Ateret Fortress; 33.0032°N, 35.6286°E; alt. 63 m a.s.l.; 7 May 1990; H. Glassmann &amp; M. Sartori leg.; MZL • 1N; same locality; 7 May 1991; H. Glassmann &amp; M. Sartori leg.; MZL • 5N; same locality; 8 Dec. 2014; Z. Yanai leg.; SMNH • 15N, 3♂; same locality; 29 Oct. 2015; Z. Yanai &amp; Y. Brenner leg.; SMNH • 14N; same locality; 16 May 2016; Z. Yanai &amp; A. Charvet leg.; SMNH • 8N; same locality; 2 Jun. 2016; Y. Hershkovitz &amp; T. Eshcoly leg.; SMNH • 3N (1N - GBIFCH00759464 - sequenced); same locality; 11 Mar. 2017; Z. Yanai &amp; J.-L. Gattolliat leg.; MZL, SMNH • 4N (2N - GBIFCH00664952, GBIFCH006759463 - sequenced); same locality; 27 Mar. 2019; Z. Yanai leg.; MZL, SMNH • 2N; Dan Stream, st. 6; 33.1320°N, 35.3845°E; alt. 120 m a.s.l.; 10 May 1990; A. Reuven &amp; M. Sartori leg.; MZL • 4N; Senir (Hasbani) Stream, upstream  Ma’ayan Barukh Bridge; 33.2253°N, 35.6152°E; alt. 103 m a.s.l.; 10 May 1990; A. Reuven &amp; M. Sartori leg.; MZL • 1N; same locality; 10 May 1991; A. Reuven &amp; M. Sartori leg.; MZL • 2N; Senir (Hasbani) Stream, downstream 'En Barukh; 33.2308°N, 35.6209°E; alt. 119 m a.s.l.; 10 May 1990; A. Reuven &amp; M. Sartori leg.; MZL • 2s♀, 1♂; same locality; 25 Jul. 1990; A. Reuven leg.; MZL • 4s♀, 3♂; same locality; 10 May 1991; A. Reuven &amp; M. Sartori leg.; MZL • 4N; Hermon (Banyas) Stream, Kefar Szold; 33.1301°N, 35.3832°E; alt. 100 m a.s.l.; 8 May 1991; A. Reuven &amp; M. Sartori leg.; MZL • 1N; Jordan River, haDodot Bridge; 32.9318°N, 35.6226°E; alt. -161 m a.s.l.; 29 Jul. 2015; Y. Hershkovitz &amp; T. Eshcoly leg.; SMNH • 2N; Jordan River, Park haYarden; 32.9091°N, 35.6235°E; alt. -203 m a.s.l.; 2 Jun. 2016; Y. Hershkovitz &amp; T. Eshcoly leg.; SMNH • 2s♂; Senir (Hasbani) Stream, Beth Hillel; 33.1989°N, 35.6108°E; alt. 82 m a.s.l.; 6 Aug. 2020; Z. Yanai &amp; A. Hershko leg.; SMNH. </p>
            <p>Male imago.</p>
            <p>Lengths. Body: up to 18 mm; forewing: up to 17 mm; cerci: up to 15 mm; caudal filament: up to 13 mm.</p>
            <p>Vertex light brown, frontoclypeus yellowish, compound eyes greyish black, base of ocelli black, ocelli whitish, antennae with pedicel light brown and flagellum medium brown.</p>
            <p>Pronotum light brown, washed with grey. Pterothorax light brown, with a large mesonotal suture yellowish. Forelegs with outer margin of femora, tibiae and tarsi medium brown, inner margin yellowish; mid- and hindlegs yellowish, with distinct inner brown maculae on the femoro-tibial articulation; wings, when folded, light brown, almost whitish when unfolded.</p>
            <p>Abdominal segments uniformly yellowish, without distinct patterns, except sides of tergite IX, tergite X and sternite IX light brown; gonostyli and cerci whitish.</p>
            <p>Forelegs functional, tibiae and tarsi of middle and hind legs weakly sclerotized and non- functional. Tarsal claws blunt. Forewing typical of the genus, with 5 groups of veins: Sc+RA, RSa+iRS, RSp+MA1, MA2+MP1, and a forked MP2+CuA - CuP vein. Subcostal field with numerous transversal veins, those issued from RA not reaching iRS in the distal forth of the length, those between iRS and MA1 only present in the proximal half.</p>
            <p> Gonostyli 4-segmented, the basal one ca. 4  × the length of segments 2 to 4 combined; a fifth segment can sometimes be present (Fig. 9B). Penis lobes with characteristic sclerotized proximal process ending in a bifid projection; lateral longitudinal lobe ending in a distinct club-shaped sclerite more than 2  × larger than the lateral lobe. Cerci with whorls of long setae at each junction. </p>
            <p>Female subimago.</p>
            <p>Lengths. Body: up to 23 mm; forewing: up to 21 mm; cerci: up to 7 mm; caudal filament: up to 5.5 mm.</p>
            <p>Colouration as in the male, except antennal pedicel entirely medium brown, forefemora with outer margin sepia, tibiae and tarsi of all legs atrophied, twisted on forelegs; tarsal claws reduced to a single pointed and unsclerotized filament. Cerci light to medium brown. Posterior margin of sternite IX deeply concave and rounded.</p>
            <p>Nymph</p>
            <p> (Fig. 10B). First described by Koch (1980) sub nomen  Oligoneuriella orontensis . </p>
            <p>Lengths. Body up to 14 mm and 19 mm in male and female nymphs respectively; cerci (and caudal filament) up to 7 mm (5 mm) and 9 mm (7 mm) in male and female nymphs respectively.</p>
            <p>General colouration light to medium brown, always lighter in male nymphs. Head medium brown, yellowish between the compound eyes. Pronotum medium brown, with yellowish areas sublaterally. Pterothorax medium brown, with yellowish maculae very characteristic (see Koch, 1980, fig. 4). Legs light brown, femora medium brown in the proximal half, lighter distally; femoro-tibial articulation darker, especially notable in mature nymphs. Setae on the outer margin of hind femora well developed, but not reaching the apex (if reaching it, then much smaller than the proximal ones) (Fig. 14F). Outer margin of hind tibiae without a row of long and thin setae (Fig. 12B). Abdominal tergites uniformly medium brown, each with a pair of light spots in the middle and one or two light maculae laterally; sternites with four spots on a transverse line and two elongated maculae anteriorly, altogether six spots creating sort of a circle (most notable in mature nymphs). Gills II-VII almost subequal in size, gill I smaller, ventral. On all gills, fibrillae shorter or subequal to lamella length. Lamellae II-VII with long and thin setae on their distal inner margin. Posteromedially sternal patch of long and thin setae present on segments II-IV(V). Posterolateral spines of the abdomen increasing in size posteriorly. Cerci uniformly dark brown, sometimes medium brown with a wide median dark band or with apex light brown.</p>
            <p>Eggs.</p>
            <p> General shape rhomboid, ca. 300  µm long and 270  µm wide, chorionic surface finely granulated (Fig. 11D), micropyle tagenoform, smooth, sperm guide well apparent (Fig. 11E),  KCT’s rather regularly arranged, ca. 10  µm of diameter, formed by coil-thread ending in a leaf-like and flat structure (Fig. 11F). </p>
            <p>Affinities.</p>
            <p> In male imagos,  O. orontensis differ from all other known species by the apex of the lateral sclerite of the penis, which is greatly enlarged, even more than in  O. dobbsi , and the proximal process of the penis which is bifid. Nymphs are characterized by a row of setae on the outer margin of hind femora which does not reach the apex compared to other species studied, except  O. jessicae to some extent, and differs to all other known species by the absence of a row of setae on hind tibiae. </p>
            <p>Habitat preference.</p>
            <p>In Israel, found in well-oxygenized streams with high water discharge and current velocity (Yanai et al. 2020). The scarcity of these habitats in the Levant may be the reason for its recent decline in Israel, and perhaps in other countries, although no recent data are available.</p>
            <p>Known distribution.</p>
            <p>Israel, Lebanon, Syria, Turkey.</p>
            <p>Comments.</p>
            <p> Al-Zubaidi and Al-Kayatt (1986) reported on "  Oligoneuriopsis sp." from northern Iraq (later cited by Abdul-Rassoul 2020). These individuals may belong either to  O. orontensis or  O. villosus , thus pushing distribution slightly eastwards or westwards, respectively. While both alternatives are possible in terms of ecology and geography, it is very likely that these specimens were misidentified and in fact belong to the genus  Oligoneuriella , the only oligoneuriid reported by the authors in the following year (Al-Zubaidi et al. 1987). Until further information is available, we ignore this report from Iraq. </p>
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	https://treatment.plazi.org/id/71EEB0A8E51957C49176844730E66534	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
295BDABD9C9D5054BD1F79A1E4D2DFB4.text	295BDABD9C9D5054BD1F79A1E4D2DFB4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis skhounate Dakki & Giudicelli 1980	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis skhounate Dakki &amp; Giudicelli, 1980 Figures 9A, 10A, 11A-C, 12A, 14E, 15E </p>
            <p> Oligoneuriopsis skhounate Dakki &amp; Giudicelli, 1980: 19, figs 14-29 (male imago, nymph). </p>
            <p>Material examined.</p>
            <p> Algeria • 1N (sequenced GBIFCH00763571); Oued Cherf, Medjez Amar; 36.44306°N, 7.31083°E; alt. 205 m a.s.l.; 3 Oct. 2018; B. Samraoui leg.; MZL • 2N (sequenced GBIFCH00763569-GBIFCH00763570); Oued Cherf, Dbabcha; 36.2166°N, 7.3181°E; alt. 610 m a.s.l.; 18 Oct. 2019; B. Samraoui leg.; MZL • Morocco • 3N; Marrakech, Palmeraie, Oued Tensift; 31.6619°N, 7.9694°W (estimated); alt. 443 m a.s.l.; 27 Apr. 1960; J. Aubert leg.; MZL • Spain • 4N;  Pyrénées , Barbastro (Huesca), Rio Vero; 42.2400°N, 0.1278°W (estimated); alt. 1000 m a.s.l.; 24 Jun. 1956; H. Bertrand leg.; MZL • 1N; Sierra Morena, Venta de Cardenas; 38.4006°N, 3.5119°W (estimated); alt. 650 m a.s.l.; 2 Aug. 1960; J. Aubert leg.; MZL • 3N; Valladolid, Cabezon, Rio Pisuerga; 41.4650°N, 5.2297°W (estimated); alt. 650 m a.s.l.; 17 Aug. 1988; D. Studemann &amp; P. Landolt leg.; MZL • 41N; Malaga, Cortes de la Frontera, Rio Guadairo; 36.5483°N, 5.3675°W (estimated); alt. 250 m a.s.l.; 21 Aug. 1988; D. Studemann &amp; P. Landolt leg.; MZL • 4N, 10s♀, 17♂; same locality; 15 Sep. 1988; P. Landolt leg.; MZL • Tunisia • 1N; Bizerte, Mateur, Oued Joumine, upstream Lake Ichkeul dam; 36.9628°N, 9.5244°E; alt. 105 m a.s.l.; 20 Nov. 2004; S. Zrelli leg.; LBE • 22N, 1s♀; same locality; 26 Jun. 2005; S. Zrelli leg.; LBE • 20N, 2s♀; same locality; 18 Jul. 2005; S. Zrelli leg.; LBE • 40N; same locality; 28 Aug. 2005; S. Zrelli leg.; LBE • 40N; same locality; 6 Sep. 2005; S. Zrelli leg.; 39 LBE, 1 MZL • 40N; same locality; 24 Oct. 2005; S. Zrelli leg.; LBE • 35N; same locality; 26 Jun. 2006; S. Zrelli leg.; 24 LBE, 11 MZL • 11N; same locality; 31 Jul. 2006; S. Zrelli leg.; LBE • 2N, 1s♀; same locality; 6 Apr. 2009; S. Zrelli leg.; MZL • 2N; same locality; 17 May 2010; S. Zrelli leg.; LBE • 5N; Tabarka, Oued Bouterfes; 36.953°N, 8.9125°E; alt. 100 m a.s.l.; 4 Jan. 2005; S. Zrelli leg.; LBE • 6N; Jandouba, Fernana, Oued Ellil; 36.7203°N, 8.7339°E; alt. 237 m a.s.l.; 28 Jul. 2005; S. Zrelli leg.; LBE • 2N; same locality; 12 Sep. 2005; S. Zrelli leg.; LBE • 4N; same locality; 29 Jul. 2006; S. Zrelli leg.; LBE • 9N; same locality; 30 Aug. 2006; S. Zrelli leg.; LBE • 10N; same locality; 26 Jun. 2008; S. Zrelli leg.; LBE • 7N; Oued Ghezala; 36.6431°N, 8.6986°E; alt. 229 m a.s.l.; 30 Aug. 2006; S. Zrelli; LBE • 5N; same locality; 21 Nov. 2009; S. Zrelli; LBE. </p>
            <p>Male imago.</p>
            <p>Adequately described and illustrated by Dakki and Giudicelli (1980). The most important character is on the genitalia where the shape of the lateral longitudinal lobe of the penis ends in a rounded sclerite a little bit larger than the lateral lobe (Fig. 9A).</p>
            <p>Nymph</p>
            <p>(Fig. 10A). Adequately described and illustrated by Dakki and Giudicelli (1980), with the following complements: setae on the outer margin of hind femora well developed and reaching the apex; outer margin of hind tibiae covered by a dense row of long and thin setae; lamella of gill I minute, fibrillae much longer than the lamella length; setae on distal inner margin of gills II-VII short and thin; posteromedially sternal patch of long setae present on segments (II)III-V, most developed on segments III-IV.</p>
            <p>Eggs.</p>
            <p> General shape rhomboid, ca. 280  µm long and 250  µm wide, (Fig. 11A) chorionic surface rather smooth, micropyle tagenoform, smooth, sperm guide well apparent (Fig. 11B),  KCT’s rather regularly arranged, ca. 10  µm of diameter, formed by coil-thread ending in a leaf-like and flat structure (Fig. 11C). </p>
            <p>Affinities.</p>
            <p> At the male adult stage,  O. skhounate is distinguished from  O. lawrencei by the presence of crossveins in the proximal part of the subcostal area, and from  O. lawrencei and  O. dobbsi by the shape of the apex of the lateral longitudinal lobe of penis sclerite which is only slightly enlarged. In the nymphal stage,  O. skhounate differs from  O. jessicae by the absence of abdominal carina and from  O. lawrencei and  O. elisabethae by the setation of the dorsal margin of hind femora with much longer setae; it also differs from  O. dobbsi by the size of gill I lamella, much longer in the latter. </p>
            <p>The ecology of the nymph in North Africa is described by Bouhala et al. (2020).</p>
            <p>Known distribution.</p>
            <p>Algeria, Morocco, Spain, Tunisia.</p>
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	https://treatment.plazi.org/id/295BDABD9C9D5054BD1F79A1E4D2DFB4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
EA1F4ECE86DB579D9A4D87D407D229AE.text	EA1F4ECE86DB579D9A4D87D407D229AE.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis sp.	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Oligoneuriopsis sp. Figure 13 </p>
            <p>Material examined.</p>
            <p>Iran • 2♂; Ghilan, Sefid-rud River, close to Rudbar [Roodbar]; app. 36.817°N, 49.433°E; alt. 180 m a.s.l.; 4 Aug. 1972; W. Heinz coll. &amp; V. Puthz leg. to MZL.</p>
            <p>Male imago.</p>
            <p> Gonostyli 4-segmented, the basal one a little bit less than 4  × the length of segments 2 to 4 combined. Segment 2 not enlarged distally, more than 2  × longer than wide. Penis lobes with sclerotized proximal process ending in a single projection; lateral longitudinal lobe ending in a distinct club-shaped sclerite ca. 2  × larger than the lateral lobe (Fig. 13). Cerci with whorls of long setae at each junction. </p>
            <p>Affinities.</p>
            <p> These two specimens are in bad state (legs missing, wings broken), but nevertheless we think it is important to report this finding. The shape of the genitalia is different from those of the previous species, somewhat intermediary between those of  O. skhounate and  O. orontensis . Second segment of gonostyli is also much slender than in the two previous species. These specimens could be the alate stages of  O. villosus , but they are reported from a far distant place (ca 700 km); hence they could also belong to a new, undescribed species. Due to these uncertainties and the lack of proper material, we prefer mentioning it without naming it. </p>
            <p>Known distribution.</p>
            <p>Iran.</p>
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	https://treatment.plazi.org/id/EA1F4ECE86DB579D9A4D87D407D229AE	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
3CC55A58256B5B3D86B5F0672FD97829.text	3CC55A58256B5B3D86B5F0672FD97829.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Oligoneuriopsis villosus Bojkova, Godunko & Staniczek 2019	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> 
Oligoneuriopsis villosus 
Bojkova
, Godunko &amp; Staniczek, 2019
 Figure 15F </p>
            <p> Oligoneuriopsis villosus Bojková , Godunko &amp; Staniczek, 2019 in Sroka et al. 2019: 113, figs 5-8 (nymph). </p>
            <p>Material examined.</p>
            <p>None.</p>
            <p>Male and female imagos.</p>
            <p>Unknown.</p>
            <p>Nymph and eggs.</p>
            <p>As described by Sroka et. al. (2019)</p>
            <p>Affinities.</p>
            <p> The nymph of  O. villosus can be easily differentiated from all other known species by the row of long and thin setae on the outer margin of hind femora reaching the apex, a row of long and thin setae on the outer margin of hind tibiae, posterolateral projections of abdominal segments diverging from body axis, the absence of posteromedian projections on abdominal terga, and posteromedian setae on sternites III-IV very long and dense. </p>
            <p>Known distribution.</p>
            <p>Iran.</p>
            <p>Comment.</p>
            <p> See comment under  O. orontensis regarding reports from Iraq. </p>
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	https://treatment.plazi.org/id/3CC55A58256B5B3D86B5F0672FD97829	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Barber-James, Helen M.;Zrelli, Sonia;Yanai, Zohar;Sartori, Michel	Barber-James, Helen M., Zrelli, Sonia, Yanai, Zohar, Sartori, Michel (2020): A reassessment of the genus Oligoneuriopsis Crass, 1947 (Ephemeroptera, Oligoneuriidae, Oligoneuriellini). ZooKeys 985: 15-47, DOI: http://dx.doi.org/10.3897/zookeys.985.56649, URL: http://dx.doi.org/10.3897/zookeys.985.56649
