Research Article |
Corresponding author: Lihong Dang ( danglihong@snut.edu.cn ) Academic editor: Elison Fabricio B. Lima
© 2023 Lihong Dang, Laurence Mound, Hongrui Zhang.
This 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.
Citation:
Dang L, Mound L, Zhang H (2023) Review of the genus Gigantothrips Zimmermann from China and Southeast Asia (Thysanoptera, Phlaeothripidae, Phlaeothripinae). ZooKeys 1169: 221-234. https://doi.org/10.3897/zookeys.1169.106733
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Gigantothrips is a genus of leaf-feeding species from the Old World tropics that is distinguished from Gynaikothrips and Leeuwenia by the large number of tergal wing-retaining setae. Eight species are recognized from China and Southeast Asia including G. tibetanus sp. nov. from Tibet and G. yunnanensis sp. nov. from Yunnan, both taken on the leaves of Ficus trees. An illustrated identification key to these eight species is provided here.
Identification key, leaf-feeding, Liothrips-lineage, new species, taxonomy, thrips
Species of the subfamily Phlaeothripinae exhibit the widest range of feeding habits in the order Thysanoptera, being known as plant-living, fungus-feeding and predators. These feeding habits largely accord with the three informal groups recognized (
Gigantothrips shares with Gynaikothrips and Leeuwenia, amongst other members of Liothrips-lineage, the following character states, metathoracic sternopleural sutures absent, mesopresternum boat-shaped, pronotum with irregular reticulate sculpture. Currently, Gigantothrips is differentiated from Leeuwenia in having the tube relatively short compared to the large body, major wing-retaining setae on tergites not fan-shaped, and the head parallel-sided with weak sculpture (
The descriptions, photomicrograph images and drawings were produced from slide-mounted specimens with a Nikon Eclipse 80i microscope. Images were prepared with a Leica DM2500 using differential interference contrast (DIC) illumination, and processed with Automontage and Photoshop v.7.0. The abbreviations used for the pronotal setae are as follows: am – anteromarginal, aa – anteroangular, ml – midlateral, epim – epimeral, pa – posteroangular. The unit of measurement in this study is the micrometre. Most specimens studied here are available in the Australian National Insect Collection (
Gigantothrips Zimmermann, 1900: 18. Type species Gigantothrips elegans Zimmermann, 1900, by monotypy.
There are now 22 species listed in this genus (
Head much longer than wide, cheeks parallel-sided with a few stout setae (Figs
1 | All tibiae clearly yellow | 2 |
– | At least mid and hind tibiae brown at base | 3 |
2 | Pronotal aa close together with midlateral setae, the distance between them shorter than their length (Fig. |
Gigantothrips tibialis Bagnall |
– | Pronotal aa far away from midlateral setae, the distance between them longer than their length (Fig. |
G. pontis (Reyes) |
3 | Tube short, no more than five times as long as basal width; S1–S2 on tergite IX acute and slightly shorter than tube (Fig. |
G. xynos (Reyes) |
– | Tube elongate, more than eight times as long as basal width; S1–S2 on tergite IX blunt and much shorter than tube (Fig. |
4 |
4 | Anterior margin of pronotum with about eight pairs of stout setae (Fig. |
G. elegans Zimmermann |
– | Anterior margin of pronotum with four pairs of setae at most | 5 |
5 | Fore tibiae clear yellow | 6 |
– | Fore tibiae largely brown or shaded with brown | 7 |
6 | Antennal segment IV with 3 sense cones; major setae stout and hyaline (Fig. |
G. nigrodentatus Karny |
– | Antennal segment IV with 2 sense cones (Fig. |
G. yunnanensis Dang & Mound, sp. nov. |
7 | Tergites II–VI with 3–4 pairs of major sigmoid setae, and numerous small sigmoid setae laterally; cheek with about 8 pairs of short and acute, but spinous setae (Fig. |
G. gallicola Priesner |
– | Tergites II–VI with two pairs of major sigmoid setae, and numerous straight setae laterally (Fig. |
G. tibetanus Dang & Mound, sp. nov. |
Gigantothrips elegans Zimmermann, 1900: 18.
20♀3♂(
Described from Java, Indonesia, this species is widespread in the tropical area from India to the Philippines, including southern China, feeding on leaves of Ficus species (
Syringothrips gallicola Priesner, 1933: 77.
Holotype
, 1♀ (
Described from Java, Indonesia, this species represented a new genus, ‘Syringothrips’, based on only a female originally. After checking the holotype female (on loan from the Senckenberg Museum, Frankfurt), it was considered to be a member of Gigantothrips and related to G. nigrodentatus from Java (
Acanthinothrips nigrodentatus Karny, 1913: 120.
1♀1♂ (
This species was described originally from Java, Indonesia, but was considered a member of Idolothripinae within the invalid genus ‘Cercothrips’ because of the large size body (Hood, 1919). After comparing the type specimens, the species was identified as belonging to the Phlaeothripinae as a species of Gigantothrips by
Gynaikothrips pontis Reyes, 1996: 112.
Holotype
, 1♀(
Described from Luzon, the Philippines, taken on Ficus pseudopalma, this species was newly combined to the genus Gigantothrips together with another Philippines species, G. xynos, based on the typical character state of the numerous pairs of tergal wing-retaining setae (
Holotype
, ♀ (SUT), China, Tibet, Motuo County, on leaves of Ficus sp., 19.vii.2022, Y.Q. Li. Paratypes, 1♀1♂ (SUT), with the same data as holotype; 1♀ (
Holotype. Female macroptera. Body brown. All femora brown, fore tibiae brownish yellow shaded with brown medially, mid and hind tibiae brown with yellowish brown at apical area, all tarsi yellowish brown. Antennae segments I–II brown, III yellow with shaded at apex, IV–V yellow with apices shaded brown, VI brown on apical half, yellow on basal half, VII–VIII brown. Wings strongly shaded with brown, body setae yellowish.
Head. Head elongate, about 2.0 times as long as wide (Fig.
Thorax. Pronotum sculptured with irregular striae and reticulation, notopleural suture complete (Fig.
Abdomen. Pelta triangular and reticulate with internal markings, with a pair of campaniform sensilla and 1–2 pairs of minute setae (Fig.
Measurements (holotype female in microns). Body length 5880. Head length 450, width just behind eyes 235; eye length 155, postocular setae length S1 30, S2 40; postocellar setae length 35; the narrowest separation between maxillary stylets 25. Antenna length 1025, segments I–VIII length (widest) 60(50), 60(40), 240(35), 190(45), 175(40), 150(35), 90(25) and 70(20), sensoria on segment III length 65. Pronotum length 240, width 400, length of pronotal setae, am 20, aa 25, ml 25, epim 115, pa 30. Fore wing length 1900, sub-basal setae length, S1 80, S2 70, S3 100. Pelta length 170, basal width 290; tergite IX posteromarginal setae S1–S3, 130, 135, 120; tube length 1050, basal width 120, apical width 70; anal setae length 230.
Male macroptera. Similar to female; but smaller, fore tarsal tooth absent; abdominal tergite IX setae S2 short; sternite VIII with a pore plate, its anterior margin like ‘W’ shape and posterior margin straight and before posterior marginal setae (Fig.
Measurements (paratype male in microns). Body length 5420. Head length 425, width just behind eyes 205; eye length 135, postocular setae length S1 30, S2 35; postocellar setae length 30; the narrowest separation between maxillary stylets 25. Antenna length 1050, segments I–VIII length (widest) 60(50), 60(35), 240(35), 185(45), 175(40), 135(40), 85(25) and 65(20), sensoria on segment III length 75. Pronotum length 250, width 365, length of pronotal setae, am 25, aa 25, ml 30, epim 110, pa 35. Fore wing length 1850, sub-basal setae length, S1 70, S2 75, S3 80. Pelta length 150, basal width 250; tergite IX posteromarginal setae S1–S3, 130, 50, 80; tube length 980, basal width 110, apical width 60; anal setae length 230.
This species name is composed of one Latin word based on the location of type specimens.
This new species was taken on the leaves of a Ficus species and it is quite similar in body shape and colouration to G. gallicola taken on the leaf-galls of Sloanea sp. in Java. However, G. tibetanus sp. nov. can be distinguished by the slender cheek setae (Fig.
Gigantothrips tibialis Bagnall, 1921: 364.
1♀(
Described from Sri Lanka on Careya arborea, this species is probably widespread in India according to
Gynaikothrips xynos Reyes, 1996: 118.
Holotype
, 1♀(
This is the third species of Gigantothrips recorded from the Philippines, and was taken on Euphorbia hirta. It has tergite IX setae S1–S3 a little shorter than the tube (Fig.
Holotype
, ♀ (
Holotype. Female macroptera. Body brown. All femora brown, fore tibiae clear yellow, mid and hind tibiae yellow with brown at basal third, all tarsi yellow. Antennae segments I–II brown with paler at extremely apices, III–V uniformly yellow, VI yellow with apices shaded, VII–VIII yellowish brown. Wings very weak shaded with brown, body setae yellowish.
Head. Head elongate, about 1.8 times as long as wide (Fig.
Gigantothrips spp. Antennal segments III–IV (15–17) 15 G. elegans 16 G. tibetanus sp. nov. 17 G. yunnanensis sp. nov.; metanotum and pelta (18) 18 G. elegans; meso and metanotum (19, 20) 19 G. tibetanus sp. nov. 20 G. yunnanensis sp. nov.; pelta (21, 22) 21 G. tibetanus sp. nov. 22 G. yunnanensis sp. nov.; tegite IV (23, 24) 23 G. nigrodentatus 24 G. tibetanus sp. nov.; tegite III (25) 25 G. elegans.
Thorax. Pronotum sculptured with irregular striae and reticulation, notopleural suture complete; two pairs of pronotal setae well developed, blunt at apex, am, aa and pa small, ml stout and elongate, epim the longest (Fig.
Abdomen. Pelta triangle and reticulate with internal markings, with a pair of campaniform sensilla and 1 pair of minute setae (Fig.
Gigantothrips spp. Tergites VIII–IX (26, 27) 26 G. pontis 27 G. xynos; pore plate on male sternite VIII (28–30) 28 G. yunnanensis sp. nov. 29 G. tibetanus sp. nov. 30 G. nigrodentatus; right side of male sternite VII (31) 31 G. tibetanus sp. nov.; tergite IX and tube (32, 33) 32 G. tibetanus sp. nov. 33 G. yunnanensis sp. nov.
Measurements (holotype female in microns). Body length 4850. Head length 430, width just behind eyes 235; eye length 120, postocular setae length S1 25, S2 30; postocellar setae length 35. Antenna length 1040, segments I–VIII length (widest) 60(50), 60(40), 215(40), 180(45), 170(45), 135(40), 100(30) and 70(15), sensoria on segment III length 60. Pronotum length 250, width 400, length of pronotal setae, am 20, aa 20, ml 40, epim 90, pa 25. Fore wing length 1700, sub-basal setae length, S1 80, S2 75, S3 100. Pelta length 150, basal width 290; tergite IX posteromarginal setae S1–S3, 155, 175, 130; tube length 780, basal width 110, apical width 60; anal setae length 195.
Male macroptera. Similar to female; but smaller, fore tarsal tooth absent; abdominal tergite IX setae S2 short; sternite VIII with a pore plate, its anterior margin like ‘W’ shape and posterior margin straight and before posterior marginal setae (Fig.
Measurements (paratype male in microns). Body length 4610. Head length 415, width just behind eyes 195; eye length 125, postocular setae length S1 50, S2 35; postocellar setae length 40. Antenna length 1000, segments I–VIII length (widest) 60(50), 60(35), 210(35), 170(40), 170(40), 150(35), 95(25) and 70(15), sensoria on segment III length 55. Pronotum length 230, width 380, length of pronotal setae, am 25, aa 30, ml 70, epim 90, pa 30. Fore wing length 1600, sub-basal setae length, S1 70, S2 80, S3 60. Pelta length 135, basal width 215; tergite IX posteromarginal setae S1–S3, 150, 70, 140; tube length 740, basal width 110, apical width 55; anal setae length 200.
This species name is composed of one Latin word based on the location of type specimens.
This new species was collected from leaves of Ficus tikoua, and it is similar in body colouration to G. nigrodentatus from Planchonia valida. It is also similar to G. tibetanus sp. nov. in body shape and pore plate on sternite VIII of male (Figs
We are grateful to Gexia Qiao (Institute of Zoology, Chinese Academy of Science, IZCAS), Liyun Jiang (IZCAS) and Kuiyan Zhang (
The authors have declared that no competing interests exist.
No ethical statement was reported.
This work was supported by the Natural Science Basic Research program of Shaanxi Province [2023-JC-QN-0178], the National Natural Sciences Foundation of China [No. 31702042], and the Second Tibetan Plateau Scientific Expedition and Research (STEP) program [Grant No. 2019QZKK0501].
Lihong Dang: writing - original draft. Laurence Mound: writing - review and editing. Hongrui Zhang: data curation.
Lihong Dang https://orcid.org/0000-0002-7571-8426
Laurence Mound https://orcid.org/0000-0002-6019-4762
Hongrui Zhang https://orcid.org/0000-0002-0089-1099
All of the data that support the findings of this study are available in the main text.