Elattoneura lapidaria Dijkstra & Bjelke
publication ID |
https://doi.org/ 10.5281/zenodo.35388 |
DOI |
https://doi.org/10.5281/zenodo.5640208 |
persistent identifier |
https://treatment.plazi.org/id/03A25264-CA35-FFDA-EEEC-FDE640ACFDAF |
treatment provided by |
Donat |
scientific name |
Elattoneura lapidaria Dijkstra & Bjelke |
status |
sp. nov. |
Elattoneura lapidaria Dijkstra & Bjelke ZBK sp. nov. – Rock Threadtail (Type Photo 9, Photos 16–17, Fig. 6)
Taxonomy
Dijkstra & Clausnitzer (2014) discussed this species and provided a photograph but no characters for identification. It belongs to the genetically and ecologically distinct glauca -group of pruinose-faced Elattoneura species, which includes E. cellularis (Grünberg, 1902) , E. frenulata (Hagen in Selys, 1860), E. glauca (Selys, 1860) , E. nigra Kimmins, 1938 , E. tarbotonorum sp. nov. and presumably E. pasquinii Consiglio, 1978 ( Tree 1). Occurs with its nearest relative E. glauca , differing in behaviour, coloration, structure and genetically. Note however, that COI data suggest that E. cellularis and E. glauca conceal additional species ( Tree 1).
Material studied
Holotype ♂. RMNH. 5007711, Zimbabwe, Manicaland, 16 km E of Chimanimani village, Chimanimani National Park, Bundi Plain and Valley, rocky sections of Bundi in grassy and boggy plain and sheltered gorge, 1510 – 1577 m a.s.l. (19.784 ° S 33.029 ° E), 01-xii- 2013, leg. K.- D.B. Dijkstra & U. Bjelke, RMNH View Materials GoogleMaps .
Further material. 3 ♂ ( RMNH.5007732 , RMNH.5007751 ), 5 ♀ ( RMNH.5007715 , RMNH.5007753 , RMNH.5007764 , RMNH.5007785 ), as holotype, RMNH View Materials View Materials View Materials View Materials View Materials View Materials GoogleMaps .
Genetics
Three unique haplotypes (n = 7) nearest to but well-separated from E. glauca from the Eastern Cape (South Africa) and even more distant from specimens of that species from northern South Africa, Tanzania, Zambia and Zimbabwe, including syntopic ones ( Tree 1).
Male morphological diagnosis
Nearest to E. glauca by (a) the pruinose face with maturity; (b) the penis with pointed apical lobes as well as slender filament-like lateral branches; and (c)the ventral process of the cerci that is wide at base, with a conspicuous subapical tooth next to the single apical tooth ( Fig. 6). However, is (1)larger, Hw 21.5–22.2 mm (n= 4) rather than 17.5–19.5 mm (n = 6); (2)darker with pruinosity on face, S 8–10 and especially thorax less dense, with only narrow ante-humeral stripes of pruinosity rather than largely pruinose mesepisterna; (3) has the penis with broader apical lobes that are laterally more round- ed and less abruptly narrowed to their fine tips; (4) the cerci with relatively shorter apex but broader ventral process; and (5) the basal part of the paraprocts longer dorsally than ventrally in lateral view; however, the appendage shape may fall within the variation of E. glauca ( Fig. 6).
Etymology
Latin “belonging to stones” refers to the adult behaviour of perching consistently on rocks (feminine adjective).
Range and ecology
Unlike most Elattoneura species, the glauca -group is associated more with exposed and/or elevated habitats than with lowland rainforest. This species occurs along open rocky streams between 1 500 and 1 600 m a.s.l. in the Chimanimani Mountains of eastern Zimbabwe ( Photo 17). Both sexes always perched flat on rocks, probably to warm up in their often misty habitat. Its sister-species E. glauca was less numerous at the same sites and rested on vegetation like grasses.
RMNH |
Netherlands, Leiden, Nationaal Natuurhistorische Museum ("Naturalis") [formerly Rijksmuseum van Natuurlijke Historie] |
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.
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