Chartocerus kerrichi ( Agarwal, 1963 )
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publication ID |
https://doi.org/10.11646/zootaxa.5696.2.1 |
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publication LSID |
lsid:zoobank.org:pub:9AF55F2A-73F8-4832-AB21-1794D74C9E8E |
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DOI |
https://doi.org/10.5281/zenodo.17401107 |
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persistent identifier |
https://treatment.plazi.org/id/03D56C3C-FFDB-4307-6EAB-57F4FD3A2F1F |
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treatment provided by |
Plazi |
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scientific name |
Chartocerus kerrichi ( Agarwal, 1963 ) |
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Chartocerus kerrichi ( Agarwal, 1963) View in CoL
Figs 30 View FIGURE 30 , 31 View FIGURE 31
Material examined. 80 ♀♀, 92 ♂♂: IRAN, West-Azarbaijan Province , Naqadeh, Solduz Wetland, 37º02′ N, 45º35′ E, 1277 m a.s.l., 21 July 2020, 29 April 2021, M. Razmi leg., ex Calamagrostis epigejos GoogleMaps .
Diagnosis (abstracted from Agarwal 1963; Hayat 1976; Schmidt et al. 2019). Females ( Fig. 30B View FIGURE 30 ) are similar to Chartocerus javensis Schmidt and Ubaidillah, 2019 and C. sumatrensis Schmidt and Polaszek, 2019 but can be distinguished from C. javensis by its shorter clava (4.5× as long as broad compared to 6.7× in C. javensis ) ( Fig. 30D View FIGURE 30 ), shorter fore wing marginal fringe (0.36–0.40× as long as width of disc compared to 0.56× in C. javensis ) ( Fig. 31E,F View FIGURE 31 ), and shorter mesotibial spur (distinctly shorter than the corresponding basitarsus in C. kerrichi but subequal in C. javensis ) ( Fig. 31C View FIGURE 31 ). It is differentiated from C. sumatrensis by its shorter ovipositor (2× as long as the mesotibia in C. kerrichi compared to 2.9× in C. sumatrensis ) ( Figs 30B View FIGURE 30 , 31D View FIGURE 31 ) and less slender clava (4.5× as long as broad in C. kerrichi compared to 6× in C. sumatrensis ) ( Fig. 30D View FIGURE 30 ). Other key characteristics of the females include a dark brown body with a metallic luster; head wider than long and semilunar in shape ( Fig. 31B View FIGURE 31 ); frontovertex approximately twice as wide as long, with a rounded occipital margin and lateral ocellus very close to eye rim ( Fig. 31A View FIGURE 31 ); eyes globular and slightly longer than wide; head with deep antennal scrobes and carinate antennal sockets near oral margin ( Fig. 31A View FIGURE 31 ); mandibles bidentate; and maxillary palps 2-segmented ( Fig. 31A View FIGURE 31 ); antenna with seven funiculars, with a cylindrical scape about 5× as long as wide, and a large pedicel ( Fig. 30D View FIGURE 30 ); mesosoma with a convex anterior margin and a straight posterior margin with distinct alutaceous sculpture ( Fig. 31D View FIGURE 31 ); fore wing hyaline with an infuscate region, and a long marginal vein ( Fig. 31E,F View FIGURE 31 ); midleg with femur having three long spines, basitarsus much shorter than tibia, and tibial spur shorter than basitarsus ( Fig. 31C View FIGURE 31 ); gaster with ovipositor sheathes slightly exserted, and with distinct subgenital and outer plates ( Fig. 31D View FIGURE 31 ).
In comparison with closely related species, males ( Fig. 30A View FIGURE 30 ) of this species characterized by the presence of a comparatively short but considerably expanded antennal clava ( Fig. 30C View FIGURE 30 ). Males exhibit a high degree of similarity in both size and body color with females. Significant distinguishing features between the sexes include the male antenna with 2 anelli, a shorter pedicel, and a long, thick clava ( Fig. 30C View FIGURE 30 ), as well as a more elongated and cylindrical body compared to the broad and laterally compressed bodies of females.
Distribution. IRAN: West Azarbaijan Province (new record). EXTRALIMITAL: India ( Type locality) ( UCD Community 2023).
Biological association. Hosts for this species are indicated in the literature to be Hemiptera , specifically from Cerococcidae , Eriococcidae , and Pseudococcidae . While this species has been found on a diversity of plants, it has been particularly documented on Saccharum officinarum ( Poaceae ) ( UCD Community 2023). During field sampling of Calamagrostis specimens, we documented limited Pseudococcidae (mealybug) populations, potentially reflecting seasonal abundance patterns. However, the concurrent presence of known mealybug predators and parasitoids suggests these hemipterans likely inhabit the plant’s phyllosphere. We emphasize the need for a detailed examination to confirm these trophic relationships.
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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Chalcidoidea |
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