2urn:lsid:arphahub.com:pub:45048D35-BB1D-5CE8-9668-537E44BD4C7Eurn:lsid:zoobank.org:pub:91BD42D4-90F1-4B45-9350-EEF175B1727AZooKeysZK1313-29891313-2970Pensoft Publishers10.3897/zookeys.636.1070610706Research ArticleAnimaliaArthropodaHexapodaInsectaInvertebrataPhlaeothripidaeThysanopteraSystematicsTaxonomyAsiaChinaA new species of Baenothrips Crawford from China (Thysanoptera, Phlaeothripidae)ZhaoChao1TongXiaolixtong@scau.edu.cn1Department of Entomology, College of Agriculture, South China Agricultural University, Guangzhou 510642, ChinaCollege of Agriculture, South China Agricultural UniversityGuangzhouChina
2016241120166366775FF85BD17-6776-FFD0-FF90-FF81FF8FFFA295CD43A2-9F48-4E1F-B3E3-7ABAEB4F81EF34848210310201617112016Chao Zhao, Xiaoli TongThis is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.http://zoobank.org/95CD43A2-9F48-4E1F-B3E3-7ABAEB4F81EF
A new urothripine species, Baenothripscuneatussp. n., is described from China. This is distinguished from its congeners by the following combination of characteristics: dorsal surface of head having a wedge-shaped reticulation extending from median to the posterior margin; antennal segments VII–VIII is closely joined with a complete suture; the mesoacrotergite strongly constricted in the middle; abdominal tergite I divided into 5 plates; width of membranous gap between ovispan on abdominal sternite IX approximately 1/3 of the apical width of segment IX.
Zhao C, Tong X (2016) A new species of Baenothrips Crawford from China (Thysanoptera, Phlaeothripidae). ZooKeys 636: 67–75. doi: 10.3897/zookeys.636.10706
Introduction
The genus Baenothrips Crawford currently comprises 11 species in the world, of which five are distributed in Asia (ThripsWiki 2016). These thrips are considered to be fungus-feeding, with most living in leaf litter, grass tussocks or dead twigs (Stannard 1970; Mound 1972; Okajima 1994). However, some species, such as B.moundi Stannard of Australia, can crawl up above soil level to grass stems, and are likely to be wind-dispersed (Mound 1972; Ulitzka and Mound 2014). The new species described below has similar dispersive behaviour, and can be collected not only in leaf litter but also on fresh leaves or stems of grass, fern, and dicotyledons. Presumably this species normally inhabits leaf litter, but crawls up fresh plants occasionally and is then dispersed by wind.
Materials and methods
The thrips were extracted by using Tullgren funnels from leaf litter, or collected by beating vegetation over a white plastic tray using a small stick, and then sorted and preserved in 90% alcohol. Specimens were then mounted into Canada balsam on microscope slides. Structural details were examined with a ZEISS Imager A1 microscope, photos were taken by a Photometrics CoolSNAP camera, and the figures were subsequently processed with Adobe Photoshop CS6. All type specimens are deposited in the
Insect Collection, South China Agricultural University
(All specimens were collected from leaf litter unless otherwise noted; females all macropterous, males all apterous).
Holotype. Female macroptera, CHINA, Guangdong province, Gaozhou County, Yuntan Town, Mt. Sanguanshan (21°55’10”N, 111°8’40”E), in leaf litter of Acaciaauriculiformis (Fabaceae), 15.xii.2014, Chao Zhao (in SCAU).
Paratypes. 8 females 1 male, taken with holotype; 3 females 7 males, same locality and habitat as holotype, 5.ix.2015, Zhaohong Wang. CHINA, Hunan: 1 female, Yanling County, Shennong Valley (26°29'N, 114°1'E), on grass stem or leaf, 15.ix.2014, Chao Zhao. 1 female, Yanling County, Shennong Valley (26°29'N, 114°1'E), in leaf litter of Cryptomeriafortune (Taxodiaceae), 16.ix.2014, Chao Zhao. Guangdong: 1 male, Shixing County, The Chebaling National Nature Reserve (24°42'N, 114°11'E), 11.x.2002, Zhiwei Li; 3 females 1 male, Huizhou City, Mt. Nankunshan (23°38'N, 113°50'E), 11.xii.2002, Zhiwei Li; 1 female, Guangzhou City, Longdong Forest Park (23°14’ N, 113°24’ E), 5.xii.2004, 1 female, in leaf litter of Acaciaauriculiformis, 1.xii.2006, Jun Wang; 1 female, Dongguan City, Mt. Yinpingshan (21°55’10”N, 111°8’40”E), on fresh leaf of Stenolomachusanum (Lindsaeaceae), 10.ix.2014, Chao Zhao; 3 females, Guangzhou City, Mt. Maofengshan (23°17'N, 113°27'E), on fresh leaf or stem of Dicranopterisdichotoma (Gleicheniaceae), 4.i.2016, Chao Zhao; 3 females, Shenzhen City, Mt. Wutongshan (22°24'N, 113°17'E), on fresh leaf or stem of Dicranopterisdichotoma, 29.iv.2016, Chao Zhao. Guangxi: 1 female, Nanning City (22°48'N, 108°22'E), on fresh leaf or stem of Pennisetumpurpureum (Poaceae), 3.x.2012 (Shulan Yang); 1 females, Shangsi County, Shiwandashan National Forest Park (25°54'N, 107°54'E), on grass stem or leaf, 25.vii.2016, Chao Zhao. Yunnan: 1 female, Jinghong City, 5.iv.1987, Xiaoli Tong. Hainan: 1 male, Baisha County, Yinggeling National Nature Reserve, Yinggezui Protection Station (18°03'N, 109°54'E), on fresh leaf of Argyreiaacuta (Convolvulaceae), 8.i.2016, Xiaoli Tong.
Description.
Female macroptera (Fig. 1): Head and prothorax dark brown; pterothorax yellowish white with dark brown anteriorly and laterally; abdominal tergites I–IX yellowish white with brown laterally, of which tergites II–V each with a pair of light brown circular patches on either side; tube yellow with extreme apex dark brown. All coxae, trochanters and apical half of tarsi brown; fore and mid femora yellowish white except for inner base brown, hind femora pale yellowish brown with brown on dorsal margins; fore tibiae yellowish white, mid tibiae yellowish yellow shaded with light brown on outer margins, hind tibiae whitish but brown medially. Antennal segment I pale brown, segments II–VI yellowish white, segments VII and VIII pale brown.
Baenothripscuneatus sp. n. 1 female habitus 2a male habitus 2b male genitalia 3 head of female 4 head of male.
https://binary.pensoft.net/fig/112340
Head (Fig. 3) almost as long as broad or a little shorter; head broadly rounded in front, with three pairs elongate cephalic setae on anterior margin; dorsal surface tuberculate and with a wedge-shape reticulation extending from middle to posterior margin; cheeks almost straight. Eyes with approximately eight facets dorsally and six ventrally, of which three dorso-lateral facets are distinctly larger than the others; three ocelli present, anterior ocellus placed between inner cephalic setae, posterior ocelli behind outer pair of cephalic setae and placed close to eyes. Antenna 8-segmented, arising ventrally (Fig. 13), segments VII–VIII closely joined with a complete suture; segment III with no sense cones, IV with two sense cones, each approximately two-thirds as long as the segment; segment V with one sense cone, situated outside of apex; segments VI and VII each with one sense cone dorsally. Maxillary stylets retracted to base of compound eyes, approximately one-third of head width apart medially.
Pronotum rectangular (Fig. 5), shorter than head, dorsal surface with irregular sculpture and wart-like tubercles; epimeral setae well developed. Mesoacrotergite strongly constricted medially by a very narrow bridge (Figs 7, 11); mesonotum sculptured with transverse dotted lines on anterior third; meta-epimeron bulging with one well developed seta. Fore wing bulging at base without basal setae; both fore wing and hind wing with a median vein or thickening, and with many, but not closely spaced, fringe cilia. Basantra weakly developed, largely membranous; ferna well developed, strongly narrowed posteromedially (Fig. 6); mesopresternum complete and transverse; mesoeusternum anterior margin entire. Mesosternal furcae fused in the middle; metasternal furcae placed laterally and widely separated (Fig. 8). All tarsi unarmed.
Baenothripscuneatus sp. n. (female) 11 mesoacrotergite 12 abdominal sternite IX (arrow indicates the ovispan) 13 antennal segments II–VIII 14 abdominal tergite I.
https://binary.pensoft.net/fig/112342
Abdominal tergite I divided into five plates, a slender median longitudinal plate bearing a campaniform sensillum (Fig. 14); tergite II with a pair of expanded wing-retaining setae; tergites III–VII with two pairs of wing-retaining setae, inner pair knife-like and outer pair fin-shaped (Fig. 9; cf. Bhatti 2002: fig 15a); tergites III–VIII posterolateral setae enlarged, each with a transverse row of 12–18 short setae medially; tergite IX 4.4 times as long as distal wide; ovispan slightly reduced, the width of membranous gap between ovispan approximately 1/3 of the apical width of segment IX (Fig. 12). Tube approximately twice as long as head with three pairs of anal setae; anal setae nearly 2.2 times as long as tube, but median dorsal pair half as long as the lateral two pairs.
Male aptera (Fig. 2a): Head with only two pairs of elongate cephalic setae on anterior margin; wedge-shape reticulation of head wider than in female (Fig. 4); abdominal tergites III–VII without brown circular patches on either side; tergites II–VII with only one pair of wing-retaining setae (Fig. 10); abdominal tergite IX nearly three times as long as distal wide. Male genitalia as in figure 2b.
Measurements (paratype male in microns). Body length 1180. Head length 120; maximum width 140; two pairs of anterior cephalic setae 42. Pronotum length 80; median width 165; epimeral setae 20. Metathoracic epimeral setae 18. Abdominal tergite IX length 120, basal width 80, distal width 40. Tube length 225, basal width 15, apical width 25; anal setae, median dorsal pair 230, lateral pairs 550. Antennal segments I to VIII length (width) as follows: 16 (27), 25 (27), 35 (23), 27 (23), 35 (21), 24 (19), 25 (15), 17 (13).
Etymology.
The specific epithet is from the Latin adjective “cuneatus” meaning wedge-shaped, and refers to the shape of reticulation on head.
Distribution.
China (Hunan, Guangdong, Guangxi, Yunnan, Hainan).
Remarks.
Only two species of the genus Baenothrips Crawford are validly recorded from China, B.cuneatus, and B.ryukyuensis Okajima. The record by Kudô (1978), of B.asper (Bournier) from China in Taiwan, was considered by Okajima (1994) to be a misidentification and to actually refer to ryukyuensis. Similarly, Bhatti (2002) suggested that the species B.asper is known only from Africa, and that the Asian records refer to some other species. Recently, B.ryukyuensis was recorded by Dang and Qiao (2014) from Fujian, China. Moreover, during sorting of specimens Baenothrips from China we found in our collections slide-mounted specimens labelled by Wang and Tong (2007) as B.murphyi (Stannard), and recognised that these actually represent B.cuneatus, the new species described above.
Baenothripscuneatus sp. n. is most closely related to B.asper (Bournier) in colour pattern and several other features, but in the new species, dorsal surface of head having a wedge-shaped reticulation extending from median to the posterior margin; the mesoacrotergite is strongly constricted medially by a very narrow bridge (Figs 7, 11) as in B.moundi (Stannard) (cf. Bhatti 2002: fig 25) and the membranous gap (Fig. 12) between the ovispan on abdominal sternite IX is much wider than those in B.asper (Bournier) (cf. Bhatti 2002: fig 18). In addition, there are other five species of the genus occurring in Asia, some of them are also similar to B.cuneatus sp. n., but this new species can be distinguish from them by the below key.
Key to Asian species of Baenothrips (female)
1
Head with two pairs of prominent anterior cephalic setae
2
–
Head with three pairs of distinct anterior cephalic setae
3
2
Two pairs of anterior cephalic setae situated laterally, and median pair of anterior cephalic setae absent; macroptera
B.quadratus
–
Only one lateral cephalic seta on either side, and one median pair of anterior cephalic setae present; aptera
B.indicus
3
Antenna 8-segmented (suture between segments VII and VIII complete)
4
–
Antenna 7-segmented; except for epimeral setae, pronotum also having a pair of well-developed midlateral setae; macroptera or brachyptera
B.minutus
4
Head with a wedge-shaped reticulation extending from median to the posterior margin; the mesoacrotergite is strongly constricted medially (Figs 7, 11); abdominal tergite I divided into five plates (Fig. 14); the width of membranous gap (Fig. 12) between ovispan is approximately 1/3 of the posterior margin of abdominal sternite IX; macroptera
B.cuneatus sp. n.
–
Head reticulate just medially; the mesoacrotergite is not constricted medially; abdominal tergite I entire; the membranous gap between the ovispan is reduced to a longitudinal narrow cleft; macroptera or aptera
5
5
Three pairs of ocelli present, lateral ocelli placed close to eyes; basantra seemingly absent; macroptera
B.murphyi
–
Ocelli absent; basantra weakly developed; aptera
B.ryukyuensis
Acknowledgements
This study was supported by the National Natural Science Foundation of China (31372236) and the Key Project for National Groundwork of Science & Technology (No.2013FY111500-5-3). We especially wish to acknowledge Zhaohong Wang, Zhiwei Li, Jun Wang, and Shulan Yang for collecting the specimens. Thanks are also due to the referees for their advice and constructive comments.
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