Euops
publication ID |
https://doi.org/ 10.5281/zenodo.188214 |
DOI |
https://doi.org/10.5281/zenodo.6221701 |
persistent identifier |
https://treatment.plazi.org/id/C84EAB6E-FFBD-FF88-64F2-07840EA0F8F2 |
treatment provided by |
Plazi |
scientific name |
Euops |
status |
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Euops View in CoL subgenus Riedeliops Alonso-Zarazaga & Lyal
Euops (Charops) Riedel, 1998: 100 ; type species, by original designation: Euops paradoxus Voss, 1935 .
Euops (Riedeliops) Alonso-Zarazaga & Lyal, 2002: 10 (replacement name for Charops Riedel View in CoL non Holmgren, 1858).
Orienteuops Legalov, 2003: 388 ; type species, by original designation: Euops tonkinensis Voss, 1933 View in CoL ; Legalov, 2008 (syn.).
Sawadeuops Legalov, 2003: 398; type species, by original designation: Attelabus punctatostriatus Motschulsky, 1860 ; syn. n.
Sawadeuops ( Nigroeuops ) Legalov, 2003: 403; type species, by original designation: Sawadeuops (Nigroeuops) ovalis Legalov, 2003 ; syn. n.
Asynaptops Legalov, 2007: 225 ; type species, by original designation: Euops keiseri Voss, 1957 View in CoL ; syn. n. Asynaptops (Asynaptopsis) Legalov, 2007: 225 ; type species, by original designation: Asynaptops (Asynaptopsis) colombensis Legalov, 2007 ; syn. n.
Riedeliops (Orienteuopsidius) Legalov, 2008: 215 ; type species, by original designation: Riedeliops (Orienteuopsidius) rasuwanus Legalov, 2008 View in CoL ; syn. n.
Diagnosis. Metanotum with one median sutural spine.
Description (based solely on species treated herein). Male. Body length: 1.52–2.70 mm.
Head short. Gena 0.66–0.75 x as long as width of head behind eyes; genae markedly converging anteriad. Vertex with row of small punctures along posterior margin of eye, without constriction behind eye, evenly rounded towards base. Eyes in dorsal view almost continuous with lateral contour of head, large, dorsally contiguous in middle for 0.4–0.7 x their length. Ventral surface shining, with transverse wrinkles except for smooth median furrow; anteriorly at base of rostrum with few scattered setae.
Rostrum 1.44–1.75 x longer than mouthparts; at widest point 1.21–1.27 x wider than at base; in cross section dorsally moderately rounded; dorsum above antennal insertions with rounded prominence; interantennal area converging anteriad with concave margins; surface subglabrous, with sparse minute punctures and if not abraded with thin recumbent setae. Venter sharply delimited against that of head, forming angle of ca. 120°, weakly convex to apex, basally with short submental median carina or without such carina; dorsal and ventral contours converging from base to apex. Prementum ( Figs. 71–72 View FIGURES 71 – 78 ) at base 1.7–1.8 x wider than long, ca. 2.3–3.9 x wider than at apex; surface flat except concavity at base of median process; sides weakly sinuate or straight, converging apicad; anteriorly with 3 moderately long apical processes, median shorter, retracted dorsad behind level of lateral processes.
Antenna ( Figs. 118–122 View FIGURES 116 – 122 ) with club relatively broad.
Proventriculus ( Figs. 101–102 View FIGURES 100 – 103 ) with eight uniform primary folds bearing thin setae or spiniform processes; without sclerotised gnathal ridges; without secondary folds; without pulvilli.
Thorax. Prothorax 0.76–0.87 x as long as wide; disc shining, subglabrous or markedly punctate-rugose with transverse or V-shaped wrinkles. Metanotum ( Figs. 79–84 View FIGURES 79 – 86 ) with small lateral lobes; with short median sutural spine ( Fig. 85–86 View FIGURES 79 – 86 ), rarely hardly projecting posteriad, but always distinctly cariniform in median sulcus. Prepectus as long as postpectus or shorter. Metasternum ventrally punctate-rugose, laterally deeply punctate. Height of pterothorax in males and females of same species identical, 0.75–0.92 x length of elytron.
Elytron 2.00–2.34 x longer than wide; humerus simple; striae deeply impressed; intervals smooth or with more or less marked transverse wrinkles.
Legs. Procoxa short, 0.88–1.06 x as long as wide (in E. trichinopoliensis 1.24 x longer than wide), simple. Femora simple, without teeth or knobs; ventral surface basally with sparse erect setae (glabrous in E. bowringii ); anterior surface dull, weakly shining, coriarious, with irregular wrinkles, granulate, with sparse recumbent setae (more shining and sculpture less marked in E. bowringii and E. trichinopoliensis ); posterior surface rather shining, with shallow wrinkles and punctures. Profemur asymmetrically clavate, dorsoventrally markedly swollen (moderately so in E. trichinopoliensis ), in dorsal aspect rather compressed, thickest at ca. 0.35–0.40 of length from apex, with inconspicuous patch of setae (except E. bowringii and E. trichinopoliensis ), at base with indistinct stalk; anterior contour convex; posterior contour almost straight; dorsal contour markedly sinuate; ventral contour convex, subapically with distinct constriction (almost straight and without constriction in E. trichinopoliensis ). Protibia in dorsal and in anterior aspect straight; dorsal contour more or less convex; ventral contour weakly sinuate, almost straight; ventral surface granulate, setose with suberect setae; uncus terminal or ventral; anterior distal comb complete ventrally; posterior distal comb oblique behind tarsal articulation, dorsal and ventral third shortened. Mesotibia ( Figs. 91–92 View FIGURES 87 – 92 , 125–129 View FIGURES 123 – 129 ) subapically with acute dorsal extension; dorsal edge of meso- and metatibia distinctly crenulate. Protarsus shorter than metatarsus; tarsomere 1 shorter than 2+3 together.
Abdomen. Sutures between ventrites 1–4 fused, almost effaced ( Fig. 97 View FIGURES 93 – 99 ) (more distinct in E. trichinopoliensis ). Venter laterally densely punctate, rugulose (sparsely punctate in E. trichinopoliensis ); disk concave or flat with shallow constriction between ventrites 4 and 5. Pygidium weakly microreticulate; densely deeply punctate (shallowly in E. trichinopoliensis ); sparsely setose.
Terminalia. Sternite VIII ( Figs. 163–167 View FIGURES 161 – 167 ) medially fully or incompletely subdivided by membrane connecting lateral sclerotised areas; apex broadly bilobate, setose; sides weakly converging in straight line from base to apex; base evenly concave or medially with marked constriction. Tegminal plate ( Figs. 66 View FIGURES 64 – 70 , 142 View FIGURES 136 – 142 , 147 View FIGURES 143 – 147 , 152 View FIGURES 148 – 152 , 157 View FIGURES 153 – 157 ) relatively broad, sides converging to evenly setose, subtruncate apex.
Females. As males except: Head with gena 0.65–0.74 x as long as width of head behind eyes. Protibia ( Figs.132–135 View FIGURES 130 – 135 ) with ventral contour sinuate; ventral surface setose with suberect setae, apically and in middle denticulate; uncus dorsal or more ventral in middle of tibial apex; ventrally with premucro. Mesotibia subapically simple, without dorsal extension. Abdomen with setose patch 1.04–1.90 x longer than wide; ventrites 1–3 each with double row of modified setae, ventrite 4 with single, inconspicuous row of sparse, unmodified setae. Ovipositor without hemisternites. Sternite VIII ( Figs. 170–173 View FIGURES 168 – 173 ) ca. 0.7 x as wide as tergite VIII; apex well defined; base without apodeme. Spermatheca as in Figs. 178, 180–182 View FIGURES 174 – 182 .
Notes. Riedeliops was proposed by Alonso-Zarazaga & Lyal (2002) as a replacement name for Charops Riedel, 1998 , a homonym inadvertently made available by the subsequent designation of a type species ( E. paradoxus Voss ) for a genus-group name proposed by Voss (1935) for two species. Although both Riedel (1998) and Alonso-Zarazaga & Lyal (2002) clearly stated that E. paradoxus is the type species of this subgenus, Legalov (2003, 2007) incorrectly listed E. armipes Voss (1933) as type species and described another genus, Orienteuops , based on E. tonkinensis Voss (1933) , a species closely related to E. paradoxus . He later ( Legalov, 2008) recognised this mistake and synonymised Orienteuops with Riedeliops , also describing another new subgenus, Orienteuopsidius . The characters used by Legalov (2003, 2007, 2008) to distinguish these genera related to Riedeliops are, however, unsuitable to define distinct genera as well as subgenera, as they are variable among closely related species and the concept of these genus-group names is far too narrow and artificial. Riedeliops is therefore here defined on more conservative characters and to include other species as well. An important character overlooked by previous authors are the sutural spines on the metanotum, a character complex investigated and shown to be of great systematic value by Riedel (2002a). These spines are generally either absent or present as a submedian pair, but a unique apomorphy occurs in some Asian species of Euops , in which they are fused into a single median one ( Figs. 81–86 View FIGURES 79 – 86 ). This character is present in Riedeliops as well as in E. punctatostriatus Motschulsky, 1860 , E. ovalis ( Legalov, 2003) and E. rasuwanus ( Legalov, 2008) , the type species of, respectively, Sawadaeuops , Nigroeuops and Orienteuopsidius , so that all these names fall into synonymy with Riedeliops . Moreover, Legalov (2007) misinterpreted E. keiseri Voss , examination of the holotype revealing this species to be closely related to E. indicus Legalov and thus to the genus Asynaptops Legalov , which is based on the latter species and therefore another synonym of Riedeliops . Euops hermanni Legalov , the type species of Rugosoeuops Legalov, 2003 , was not examined and the status of this generic taxon is therefore currently impossible to assess, but if Legalov´s phylogeny ( Legalov, 2003, fig. 1275) is taken as evidence, its proximity to Nigroeuops and Sawadaeuops makes its synonymy with Riedeliops likely. The same applies to a number of other taxa, such as Leveuops, Vieteuops and Riedeliopsis , that were included by Legalov (2007) as subgenera of Riedeliops . Since critical characters are not given in the original descriptions, their type species should be examined before a final decision on their status is made. These various ill-defined genus-group names aside, a distinct species-group exists in Riedeliops that can be readily delimited by the following characters: a protrusion of the mesonotum ( Fig. 77 View FIGURES 71 – 78 ), ventrite 4 in the male medially with a more or less conspicuous setose brush with pores at the base ( Figs. 93–98 View FIGURES 93 – 99 ) and a fairly uniform flagelliform shape of the TA ( Figs. 144–145 View FIGURES 143 – 147 , 149–150 View FIGURES 148 – 152 , 154–155 View FIGURES 153 – 157 ). This species group is here referred to as the indicus -group, and it currently comprises E. indicus Legalov , E. pseudoindicus sp. n. and E. keiseri Voss , and possibly also E. barbieri Marshall.
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.
Kingdom |
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Phylum |
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Class |
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Order |
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SuperFamily |
Curculionoidea |
Family |
Euops
Riedel, Alexander 2009 |
Riedeliops (Orienteuopsidius)
Legalov 2008: 215 |
Asynaptops
Legalov 2007: 225 |
Legalov 2007: 225 |
Orienteuops
Legalov 2003: 388 |
Euops (Riedeliops)
Alonso-Zarazaga 2002: 10 |
Euops (Charops)
Riedel 1998: 100 |