Research Article |
Corresponding author: Xiao Hui Hou ( hxh19801122@163.com ) Academic editor: Art Borkent
© 2020 Xue Lu, Chen Duan, Yuan Ning, Xiao Hong Jiang, Xiao Hui Hou.
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:
Lu X, Duan C, Ning Y, Jiang XH, Hou XH (2020) Morphology of the immature stages of Dasyhelea silvatica Wang, Zhang & Yu with redescriptions of adults (Diptera, Ceratopogonidae). ZooKeys 961: 119-127. https://doi.org/10.3897/zookeys.961.53882
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The immatures of the biting midge Dasyhelea silvatica are described and illustrated for the first time and a complete description of the adult male and female are provided using scanning electron and compound microscopes. The specimens were collected from flooded soil near a pond in Guizhou Province, China, and reared in the laboratory.
Adult, aquatic, biting midge, fourth instar larva, pupa
Biting midges of the genus Dasyhelea Kieffer, 1911 (Diptera, Ceratopogonidae) are a large and complex group of Ceratopogonidae with diverse morphology and biology, and are cosmopolitan in distribution except in Antarctica (
Larvae and pupae of D. silvatica were collected from flooded soil in Xiaojiawan, Guizhou Province in 2018, using a small shovel, and transferred to the laboratory. The larvae were individually placed in 24-well plates and fed with a sterile nutrient solution of Chlorella. Once they pupated, they were isolated in ampoule bottles on filter paper with sugar water. They were reared in an environmental chamber maintained at a temperature of 28 ± 2 °C, a relative humidity of 75 ± 2%, and a photoperiod of 12 h light and 12 h dark, and observed daily until adult emergence. The emergent adults, whole larvae, and pupae were preserved in ethanol at each stage. The specimens were mounted in Canada balsam following the technique described by
For the SEM study, one larva of D. silvatica was prepared following the technique of
Dasyhelea (Dasyhelea) silvatica Wang, Zhang & Yu, 2014: 312 (male and female, China).
3 males with pupal exuviae, 4 females with pupal exuviae, 3 fourth instar larvae, 2 larval exuviae. Xiaojiawan Village, Xinpu New District, Zunyi City, Guizhou Province, China, 27°43'22.83"N, 107°04'27.62"E, 7.VII.2018, alt. 866 m, Chen Duan leg. 2 larvae examined by SEM. Same data as above.
Fourth instar larva (Fig.
Dasyhela silvatica Wang, Zhang & Yu, fourth instar larva A chaetotaxy on the head capsule, lateral view (SEM) B chaetotaxy on the head capsule, ventral view C detail of labrum D sensilla coeloconica E detail of scopae F detail of mouthparts G caudal segment H head, ventral view I hypopharynx J epipharynx. Abbreviations: antenna (AN); epipharynx (epy); galeolacinia (GL); hypostoma (HY); hooks (H); hypopharynx (hyp); labrum (LB); lacinial sclerite 1 (LC1); lacinial sclerite 2 (LC2); mandible (MD); maxilla (MX); maxillary palpus (MP); messors (MS);palatum (PL); sensilla coeloconica (Sco); sensilla campaniformia (Sca); scopae (Sc); first lateral setae (l1); second lateral setae (l2). Scale bars: 0.1 mm (G–I).
Pupa (Fig.
Dasyhelea silvatica Wang, Zhang & Yu. Male pupa (A–H), female pupa (I, J) A, I dorsal apotome B segment 9 C clypeal/labral sensilla and ocular sensilla D metathoracic sensilla, and first abdominal segment E anterolateral and anteromedial sensilla F dorsal and supra-alar sensilla G dorsolateral cephalic sclerite sensilla H segment 4 J segment 9. Abbreviations: Anterolateral sensilla (AL-1-T, AL-2-T, AL-3-T); clypeal/labral sensilla (CL-1-H, CL-2-H); dorsal apotome sensilla (DA-1-H, DA-2-H); dorsolateral cephalic sclerite sensilla (DL-1-H, DL-2-H, DL-3-H); dorsal setae (D-1-T, D-2-T, D-3-T); dorsal sensilla of segment 9 (D-5-IX); methatoracic sensilla (M-2-T, M-3-T); ocular sensilla (O-1-H, O-2-H) respiratory organ (RO); tergite 1 sensilla (D-2-I, D-4-I, D-7-I, L-1-I, L-2-I, L-3-I); genital lobe (GL); terminal process (TP). Scale bars: 0.1 mm.
Female. Similar to male with usual sexual differences. General coloration of exuviae pale brown, except dorsolateral cephalic sclerite brown. Dorsal apotome (Fig.
(Fig.
Thorax. Scutum shallow, scutellum yellow, with ten stout setae. Legs light brown, hind tibial comb with seven spines (Fig.
Abdomen. Brown. Genitalia: tergite 9 nearly trapezoidal with prominent, long with apical stout seta, apico-lateral processes. Posteromedial margin of sternite 9 with inconspicuous projection, Gonocoxite stout, 1.73 X longer than greatest width, gonostylus slender (Fig.
Female
(Fig.
Thorax. Wing length 1.29–1.34 (1.22, N = 2) mm, width 0.51–0.54 (0.53, N = 2) mm, CR 0.48 (Fig.
Abdomen. Similar to male. Subgenital plate (Fig.
China (Fujian Province, Guizhou Province).
Dasyhelea silvatica Wang, Zhang & Yu. Male adult (A–J), female adult (K–T) A, K frontal sclerite, anterior view B, L eyes contiguous, anterior view C, M flagellomeres, anterior view D, N clypeus, anterior view E, O palpus, anterior view F metatibial distae comb G genitalia, ventral view H genitalia, ventral view I aedeagus J paramere P wing Q hind tibial comb R subgenital plate and spermatheca, ventral view S subgenital plate, ventral view T spermatheca, ventral view. Scale bars: 0.1 mm.
Dasyhelea silvatica belongs to the subgenus D. (Dasyhelea) (
The common characteristics of the pupae of D. silvatica and D. azteca are as follows: the small rounded tubercles on cephalothorax; the surface of dorsal apotome also has rounded tubercles; the abdominal segments covered with spinules, and the sensilla of the fourth abdominal segment are all located on flattened tubercles. But the pupa of D. azteca differs from D. silvatica by having a single ocular sensillum, the exuviae is brown in general coloration, and the RO has 22–24 apical and three or four lateral pores, and without a pedicel. The pupa of D. silvatica is similar to D. flavifrons by virtue of the three dorsolateral cephalic sclerite sensilla and the tergite of the first abdominal segment with the L-1-IV represented by a long and stout seta, but the one ocular sensilla, the RO bearing 14–16 apical and four or five lateral pores, anterolateral sensilla with AL-1-T, AL-2-T long, thin seta and AL-3-T short, stout seta distinguish from D. silvatica. Furthermore, the pupa of D. silvatica is similar to that of Dasyhelea eloyi Díaz & Ronderos, 2013 with small rounded tubercles on cephalothorax surface and the RO with scale-like spines, but the latter has 6–8 lateral pores compared to D. silvatica with 5 lateral pores.
Finally, we found a semicircular, transparent membrane, strongly varying in shape, present at the trailing edge of the epipharynx of D. silvatica.
We are indebted to Professor Run Zhi Zhang for providing us with the assistance of the laboratory platform, to Dr Kui Yan Zhang for technical assistance, and to Dr Art Borkent for providing many useful suggestions. Also, we would also like to acknowledge the critical review of the manuscript by Dr Florentina Díaz. This research was affirmed and financially supported by a grant from the National Natural Science Foundation of China (No. 81802040, 31960102) and Science and Technology Joint Fund Project of Zunyi Science and Technology Bureau and Zunyi Medical University (No. HZ [2019] 30).