taxonID	type	description	language	source
03B6DC38FFB6FFFDB5B6FF1F3D13FB9E.taxon	description	Figs. 1 – 10. Rhopalopsole vespertilio Chen & Du, 2017. Zootaxa, 4319 (1): 185.	en	Chen, Zhi-Teng (2020): The larvae of Rhopalopsole vespertilio Chen & Du (Plecoptera: Leuctridae) with biological notes on sympatric Nemoura nankinensis Wu (Plecoptera Nemouridae). Zootaxa 4767 (4): 578-588, DOI: 10.11646/zootaxa.4767.4.7
03B6DC38FFB6FFFDB5B6FF1F3D13FB9E.taxon	materials_examined	Material examined. Twenty-eight male adults, six female adults, one male larva, four female larvae and three exuviae, China: Jiangsu Province, Jurong City, Mt. Maoshan (Fig. 1 A-F), 31 ° 47 ′ 15 ″ N, 119 ° 18 ′ 23 ″ E, 160 m, 5 March 2020, leg. Zhi-Teng Chen (ICJUST). Mature larva. Body length 7.0 – 8.0 mm. General color pale brown, appendages generally pale (Figs. 2 – 3). Head slightly elongate, oval shaped (Fig. 4 A – B), frontal area with two oblique fusiform sclerites connected by anterior ocellus (Fig. 4 A); labrum glabrous at anterior half, medially with a transverse row of pale, short hairs, posterior half mostly spinulose but with two small glabrous areas on each side of median line; clypeus broad and elliptical, medially elevated; epicranial suture pale. Three ocelli, reddish; compound eyes dark and glabrous; several glabrous areas present near the anterior and posterior lateral ocelli. Antennae slender (Fig. 4 C – F), slightly shorter than half of body length, basal ⅔ covered with dense bristles and apically fringed with several short bristles, apical ⅓ nearly gla- brous, pale with very short apical spines. Mouthparts typical euholognathan, glossa and paraglossa of labium knobshaped, equally short (Fig. 4 B); labial palp short, three-segmented (Fig. 4 B); maxillary palp five segmented (Fig. 5 A – B); stipes of maxilla basally covered with sparse long spines; galea hook-shaped, outer margin of basal half fringed with several long bristles, apex with several short spines, inner margin glabrous; lacinia subtriangular and slightly sclerotized, with a long apical tooth and a comb with approximately 16 marginal spines. Mandible with four major unserrated apical teeth, base of the anterior pair of apical teeth with a short row of approximately 8 spines; marginal comb of about 15 thick spines posterior of the apical pair of teeth (Fig. 5 C – D). Mentum pale; posterior half of submentum with two oblique, elliptical pale areas (Fig. 4 B). Cervix short, ventral aspect with two anterolateral conical sclerites (Fig. 4 B). Pronotum subquadrate with obtuse corners (Fig. 4 A), mostly brown, covered by dense spinules, anterior and posterior transverse sutures dark. Meso- and metanota covered with sparse short bristles (Fig. 4 G); wing pads of mesonotum elongate, slightly constricted basally (Fig. 4 G – H); wing pads of metanotum shorter, widened at basal half; dorsal aspects of wing pads scattered with irregular, black, short bristles. Coxae membranous and glabrous dorsally (Fig. 4 A, G), but ventrally and laterally spinulose (Fig. 4 B, H); trochanters ventrally spinulose. Femora dorsally and ventrally covered with dense short spines except for a glabrous longitudinal median stripe (Fig. 6 E – F), outer margin with sparse short spines and moderately long swimming hairs which shorten towards each end of femora, inner margin with two longitudinal rows of dark spines along the two ridges. Tibiae evenly covered with short spines except for a glabrous longitudinal median stripe on apical half of dorsal and ventral surfaces, outer margin with sparse short spines and moderately long swimming hairs which shorten towards each end, inner margin with two longitudinal rows of dark spines; two large tibial spurs present ventrally. Tarsal segments spinulose, outer margins with sparse short swimming hairs. Claws sharp and slender, apically sclerotized (Fig. 6 A – F). In male larvae: abdominal terga 4 – 7 and sterna 3 – 6 evenly covered with black short spines (Figs. 2, 7 A – B); terga 2 – 8 each with two fusiform lateral sclerites; terga 3 – 8 each with four small adult muscle scars visible beneath larval cuticle; anterior margins of terga 1 – 9 with medially interrupted adult sclerites beneath exoskeleton. Tergum 9 with long spines less in number than previous segments, two transverse sclerites of adult present beneath exoskeleton of posterior margin. Posterior half of tergum 10 glabrous, rounded and elevated, enclosing a hook-shaped epiproct. Sterna 2 – 6 each with two black pits and anterolateral sclerites; an elliptical adult vesicle visible below sternum 9; paraprocts mostly glabrous, basally with several dark spines, apically with a single pale, long hair on each paraproct. Cerci mostly pale, much shorter than abdomen; basal cercal segment spinulose and brown, other segments pale; each segment with several long apical bristles, length of which does not exceed the segment length (Figs. 2, 8). In female larvae: abdominal terga 1 – 9 and sterna 1 – 7 evenly covered with black short spines (Figs. 3, 9); terga 2 – 8 each with two fusiform lateral sclerites; terga 2 – 8 each with four small dark pits; tergum 9 with two small dark pits; tergum 10 with two anterolateral sclerites and five glabrous spots, posterior margin humped. Sterna 2 – 3 each with two small anterolateral sclerites; posterior margin of sternum 7 with a glabrous median area; Sternum 8 with a funnel-shaped membranous area which with an inverted Y-shaped patch of long spines. Sternum 9 with two glabrous triangular areas on each side of median line. Paraprocts membranous, apically with one or two pale, long hairs on each paraproct. Cerci similar to male.	en	Chen, Zhi-Teng (2020): The larvae of Rhopalopsole vespertilio Chen & Du (Plecoptera: Leuctridae) with biological notes on sympatric Nemoura nankinensis Wu (Plecoptera Nemouridae). Zootaxa 4767 (4): 578-588, DOI: 10.11646/zootaxa.4767.4.7
03B6DC38FFB6FFFDB5B6FF1F3D13FB9E.taxon	diagnosis	Diagnosis. Rhopalopsole vespertilio is the second Chinese species of Rhopalopsole of which the larva has been associated. As with R. hamata, larvae of R. vespertilio exhibit similar maxilla and cerci, but the mandible has larger apical teeth; the head, pronotum, and abdomen have dark brown markings; antennae and legs with apparently different spine patches (see figs. 4 – 7 in Chen 2019). However, since only two larvae of the 56 Chinese species have been described, any direct comparisons await further larval associations in this genus. Biological notes. Unlike the sympatric N. nankinensis, R. vespertilio was found only in smaller (less than two meters wide) upstream sections with increase flows (Fig. 1 C – F). As is typical of many leuctrids, larvae of R. vespertilio were associated with leaf packs. Larvae typically exhibited serpentine movement (Fig. 10 A – C). Larvae moved to the upper surface of the leaves to emerge, then flew to nearby riparian vegetation (Fig. 10 D – G). After emergence, larvae darkened with the first color change occurring with the pronotum (Fig. 10 H – J). No obvious drumming behavior were observed for R. vespertilio.	en	Chen, Zhi-Teng (2020): The larvae of Rhopalopsole vespertilio Chen & Du (Plecoptera: Leuctridae) with biological notes on sympatric Nemoura nankinensis Wu (Plecoptera Nemouridae). Zootaxa 4767 (4): 578-588, DOI: 10.11646/zootaxa.4767.4.7
03B6DC38FFBFFFFCB5B6FB2F3A23F844.taxon	description	Fig. 11.	en	Chen, Zhi-Teng (2020): The larvae of Rhopalopsole vespertilio Chen & Du (Plecoptera: Leuctridae) with biological notes on sympatric Nemoura nankinensis Wu (Plecoptera Nemouridae). Zootaxa 4767 (4): 578-588, DOI: 10.11646/zootaxa.4767.4.7
03B6DC38FFBFFFFCB5B6FB2F3A23F844.taxon	materials_examined	Material examined. Forty-nine males, five females, four larvae, China: Jiangsu Province, Jurong City, Mt. Maoshan (Fig. 1), 31 ° 47 ′ 15 ″ N, 119 ° 18 ′ 23 ″ E, 160 m, 5 March 2020, leg. Zhi-Teng Chen (ICJUST). Biological notes. Nemoura nankinensis and R. vespertilio were the only two stonefly species collected during our trip at Mt. Maoshan. Larvae of N. nankinensis inhabited leaf packs and also undersides of small stones (Fig. 11 A). The newly emerged male adults, typical of many nemourids, could be found on top of dry rocks (Fig. 11 B – D). Apparently, males drummed by bending the abdomen and tapping rock surfaces (Fig. 11 E – F). Adults and larvae of N. nankinensis were collected along most sections of the mainstream flowing from the peak of the mountain into the valley. This species occurred from rapid-flowing sections of the stream to areas where the stream became subterranean. Several adults were found even along a valley section with no flow and much submerged filamentous algae and macrophytes. Several years ago, this section of the stream was a fast flowing (Fig. 11 G – H). Acknowledgments I am grateful to Prof. Yu-Zhou Du and Yangzhou University for teaching me the taxonomy of the Plecoptera. I am also grateful to Dr. Boris Kondratieff and anonymous reviewers for helpful comments and manuscript improvement. This work is funded by the Start-up Funding of Jiangsu University of Science and Technology (1182931901).	en	Chen, Zhi-Teng (2020): The larvae of Rhopalopsole vespertilio Chen & Du (Plecoptera: Leuctridae) with biological notes on sympatric Nemoura nankinensis Wu (Plecoptera Nemouridae). Zootaxa 4767 (4): 578-588, DOI: 10.11646/zootaxa.4767.4.7
