ZooKeys 111: 1–10, doi: 10.3897/ZooKeys.111.1283
Asiphonipponaphis, a new genus of Hormaphidinae (Hemiptera, Aphididae) causing galls on Distylium chinense from China, with description of a new species
Jing Chen1,3,†, Masato Sorin2,‡, Ge-Xia Qiao1,§
1 Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, No. 1 Beichen West Road, Chaoyang District, Beijing 100101, P.R.China
2 Kogakkan University, 30–64, Sakuragaoka, Ise-shi, Mie-ken, 516–0028, Japan
3 Graduate University of Chinese Academy of Sciences, No. 19 Yuquan Road, Shijingshan District, Beijing 100049, P.R.China

Corresponding author: Ge-Xia Qiao (qiaogx@ioz.ac.cn).

Academic editor: Mike Wilson

received 19 March 2011 | accepted 19 May 2011 | Published 22 June 2011


(C) 2011 Jing Chen. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


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Abstract

The aphid genus Asiphonipponaphis gen. n. from China is new to science. Asiphonipponaphis vasigalla sp. n. causing galls on Distylium chinense from Hunan, China is described and illustrated. Holotype and paratypes are deposited in the National Zoological Museum of China, Institute of Zoology, Chinese Academy of Sciences, Beijing, China (NZMCAS) and Kogakkan University, Japan.

Keywords

Asiphonipponaphis, Aphididae, Hormaphidinae, new genus, new species, China

Introduction

The aphid tribe Nipponaphidini in subfamily Hormaphidinae (Hemiptera: Aphididae) occurs in East and Southeast Asia, with Distylium as the primary host, on which different shaped and sized galls are produced, and Fagaceae, Lauraceae and Moraceae as the secondary hosts (Ghosh 1988). Pergande (1906) described the first nipponaphidine species causing galls on Distylium from Japan. Since then, many gall-forming species on Distylium have been described (Matsumura 1917, Monzen 1934, 1954, Takahashi 1958, 1962, Hille Ris Lambers 1959, Noordam 1991, Sorin 1996). Takahashi (1962) and Sorin (1987) reviewed the species which cause galls on Distylium in Japan. Blackman and Eastop (1994) keyed the aphid species on Distylium, including free-living apterae and alatae emerging from galls. Sorin (2003) keyed the aphid species living on Distylium racemosum in Japan based on the galls and their detailed life cycles.

Up to now, at least eighteen species and one subspecies in twelve genera are known to induce galls on Distylium. Thirteen species and one subspecies are recorded on Distylium racemosum, viz. Dinipponaphis autumna (Monzen), Indonipponaphis fulvicola Sorin, Metanipponaphis cuspidatae (Essig & Kuwana), Metanipponaphis rotunda Takahashi, Metanipponaphis rotunda nakijinensis Sorin, Metathoracaphis isensis Sorin, Monzenia globuli (Monzen), Monzenia ihai Sorin, Neothoracaphis yanonis (Matsumura), Nipponaphis distychii Pergande, Nipponaphis distyliicola Monzen, Nipponaphis loochooensis Sorin, Nipponaphis monzeni Takahashi and Quadrartus yoshinomiyai Monzen. Five species are recorded on Distylium stellare, viz. Distylaphis foliorum (van der Goot), Neohormaphis calva Noordam, Reticulaphis distylii (van der Goot), Schizoneuraphis gallarum van der Goot and Schizoneuraphis longisetosa Noordam. In China, Neothoracaphis yanonis also forms galls on Distylium chinense (personal observation).

In this study, a new genus and a new species, Asiphonipponaphis vasigalla sp. n. causing galls on Distylium chinense is described from Hunan, China, further enriching the group of aphid species forming galls on Distylium.

Materials and methods

All specimens examined in this study were collected from Jishou University (Jishou City) by X. T. Li.

Aphid terminology in this paper generally follows Ghosh (1988) and Noordam (1991). The unit of measurements in this paper is millimeters (mm).

In Table 1, the following abbreviations have been used: Ant.I, Ant.II, Ant.III, Ant.IV, Ant.Vb, for antennal segments I, II, III, IV and the base of antennal segment V, respectively; PT, processus terminalis; Ant.IIIWD, the widest diameter of antennal segment III; URS, ultimate rostral segment; BW URS, basal width of ultimate rostral segment; 2HT, second hind tarsal segment; MW hind tibia, mid-width of hind tibia; BW Cauda, basal width of cauda; AP, anal plate; GP, genital plate.

Specimen depositories: the holotype and ten paratypes of the new species are deposited in the National Zoological Museum of China, Institute of Zoology, Chinese Academy of Sciences, Beijing, China (NZMCAS), and two paratypes in Kogakkan University, Japan.

Table 1.

Biometric data of Asiphonipponaphis vasigalla sp. n. (in mm).

Parts(For abbreviations see Materials and methods) Fundatrix (n=1) Alate vivipara (n=10)
Mean Range Standard Deviation
Length (mm) Body length 2.036 2.394 2.204–2.492 0.098
Body width 1.723 1.162 1.126–1.219 0.029
Ant.I 0.057 0.062 0.052–0.073 0.008
Ant.II 0.043 0.048 0.045–0.051 0.003
Ant.III 0.189 0.406 0.371–0.443 0.023
Ant.IV / 0.183 0.156–0.203 0.015
Ant.Vb / 0.076 0.065–0.085 0.007
PT 0.026 0.026 0.020–0.032 0.004
URS 0.063 0.068 0.065–0.071 0.003
Hind femur 0.342 0.532 0.516–0.548 0.009
Hind tibia 0.301 0.684 0.661–0.701 0.012
2HT 0.072 0.106 0.099–0.111 0.004
Cauda 0.025 0.048 0.043–0.050 0.002
BW Cauda 0.035 0.054 0.050–0.057 0.003
Ant.IIIWD 0.038 0.051 0.048–0.056 0.002
MW Hind tibia 0.035 0.039 0.035–0.042 0.002
Cephalic setae 0.026 0.013 0.012–0.017 0.002
Setae on Tergum I 0.023 0.022 0.015–0.027 0.004
Setae on Tergum VIII 0.038 0.037 0.032–0.041 0.003
Setae on Hind tibia 0.024 0.031 0.027–0.033 0.002
No. of setae on Ant.I 2 1–3
Ant.II 2 2
Ant.III 0 0
Ant.IV 0 0
Ant.Vb 0 0
PT 0+4 0+5
URS 6 6
Tergum VIII 4 5–8
Cauda 9 12–19
Each lobe of AP 9–10 10–15
GP 13 39–52
Ratio (times) Whole antenna / Body 0.14 0.33 0.32–0.35 0.009
Hind femur / Ant.III / 1.32 1.21–1.48 0.084
Hind tibia / Body 0.15 0.29 0.28–0.31 0.012
PT / Ant.Vb / 0.35 0.24–0.48 0.071
URS / BW URS 1.43 1.29 1.09–1.55 0.159
URS / 2HT 0.88 0.65 0.61–0.71 0.037
Cauda / BW Cauda 0.74 0.90 0.80–1.01 0.071
Cephalic setae / Ant.IIIWD 0.68 0.26 0.22–0.33 0.032
Setae on Tergum I / Ant.IIIWD 0.61 0.43 0.29–0.53 0.078
Setae on Tergum VIII / Ant.IIIWD 1.01 0.72 0.58–0.80 0.067
Setae on hind tibia / MW Hind tibia 0.68 0.79 0.68–0.92 0.081
Taxonomy
Type species.

Asiphonipponaphis vasigalla sp. n.

Etymology.

The new genus is named for the absence of siphunculi. “A” (Latin) means “absent”, “sipho” (Latin) means “siphunculi”, “nipponaphis” refers to its affiliation to the tribe Nipponaphidini.

Generic diagnosis.

In alatae, antennae 5-segmented, secondary rhinaria annular. Rostrum short, ultimate rostral segment shorter than second hind tarsal segment, with 2 pairs of primary setae and 1 pair of accessory setae. Abdomen with 5 pairs of spiracles, present on abdominal segments II–VI. Siphunculi absent in both fundatrix and emigrant alatae. Cauda knobbed, distinctly constricted at base. Anal plate bilobed. Legs normal. Tarsi 2-segmented, claws normal, first tarsal chaetotaxy of alatae 3, 3, 3. Fore wings of emigrant alatae with pterostigma narrow and long, distal margin of pterostigma forming almost a straight line with the hind margin, media unbranched, not united with cubitus, and two cubitus veins fused at base; hind wings with 2 obliques.

Comments.

This new genus is unique in Nipponaphidini by its peculiar galls and morphological characters. Different from other saccate galls on Distylium, e.g. galls of Nipponaphis, its galls are located on the midrib of leaves and split at the tip when mature, forming a flower-shaped opening, while galls of Nipponaphis are located on twigs and usually open on the lateral wall of the galls when mature. It is related to Quadrartus Monzen for sharing several characters in alatae, such as spiracles present on abdominal segments II–VI (i.e. 5 on each side of abdomen), distal margin of pterostigma forming almost a straight line with the hind margin, but differs from the latter as follows: antennae 5-segmented (in Quadrartus: 4-segmented); media of fore wings unbranched (in Quadrartus: once branched); siphunculi absent (in Quadrartus: present). It is also related to Indonipponaphis Ghosh & Raychaudhuri. Both of them possess 5-segmented antennae in alatae and induce galls on the midrib of leaves of Distylium. But the new genus differs from Indonipponaphis as follows: abdomen with 5 pairs of spiracles (in Indonipponaphis: 4 pairs); media of fore wings unbranched (in Indonipponaphis: once branched); siphunculi absent (in Indonipponaphis: present).

Taxonomy of Nipponaphidini is mostly based upon the apterae on secondary hosts. The identification of alatae is much more difficult because of the vague descriptions and limited diagnostic characters. But not all species are known by both alate and apterous morphs. Thus identification of alatae, although confusing, is still very important to the classification of Nipponaphidini. Further observations of life cycles will probably reveal more gall causers on Distylium, and acquisition of more morphs will facilitate the taxonomic study and clear up the confusion.

Figures 1–7.

Asiphonipponaphis vasigalla sp. n. Fundatrix 1 antenna. Alate viviparous female(emigrant from galls) 2 antenna 3 ultimate rostral segment 4 fore wing 5 cauda 6 anal plate 7 genital plate. Scale bars = 0.10 mm.

Locus typicus.

China (Hunan, 28°17'23"N, 109°43'11"E, altitude 240 m).

Etymology.

The new species is named for the shape of gall. “Vas” (Latin) means “vase”, “galla” (Latin) means “gall”.

Description.

Fundatrix: Body oval, nearly round (Fig. 8), reddish brown and covered with thin white wax in life. For morphometric data see Table 1.

Mounted specimens.

Body lightly sclerotized, pale in color. Antennae, ultimate rostral segment and legs brown. Head, thorax and abdominal segments I–VII completely fused. Dorsum smooth. Abdominal tergite VIII with dense spinulose imbrications. Spiracles oval, closed, on abdominal segments II–IV, spiracular plates light brown. Dorsal setae of body little, short and pointed. Head with 1 pair of cephalic, 1 pair of spinal, 1 pair of pleural and 1 pair of marginal setae; thoracic nota each with 1 pair of spinal, 1 pair of pleural and 2 pairs of marginal setae; abdominal tergites I–VI each with 1 pair of spinal, 1 pair of pleural and 1 pair of marginal setae; tergite VII with 1 pair of marginal setae; tergite VIII with 4 setae. Cephalic setae, marginal setae on abdominal tergite I and setae on tergite VIII 0.68 times, 0.61 times and 1.01 times as long as widest diameter of antennal segment III, respectively. Front straight. Eyes 3-faceted. Antennae 3- or 4-segmented (Fig. 1); 0.14 times as long as body. Length in proportion of segments I–III: 35 : 26 : 100+16, respectively. Processus terminalis 0.16 times as long as base of the segment III; very thin, basal width 0.47–0.57 times as long as apical width of base of the segment III. Setae on antennae sparse. Segments I–III each with 2, 2, 0+0 setae, respectively. Processus terminalis with 4 apical setae. Primary rhinaria small, round, protuberant and placed wide apart. Rostrum short and thick, not reaching mid-coxae. Ultimate rostral segment blunt wedge-shaped, 1.43 times as long as its basal width, 0.88 times as long as second hind tarsal segment; with 2 pairs of primary setae and 1 pair of accessory setae. Legs normal. Trochanters and femora fused. Hind trochanter and femur 2.11 times as long as the base of antennal segment III, hind tibia 0.15 times as long as body. Setae on legs sparse, fine and pointed. Setae on hind tibia 0.68 times as long as its mid-diameter. First tarsal chaetotaxy: 2, 2, 2. Siphunculi absent. Cauda, anal plate and genital plate with dense spinulose imbrications. Cauda knobbed, indistinctly constricted at base, 0.74 times as long as its basal width, with 9 setae. Anal plate bilobed, each with 9 or 10 setae. Genital plate broad round, with 2 anterior setae and 11 setae along the posterior margin. Two gonapophyses each with 3 or 4 short setae.

Alate viviparous females (emigrants from galls): Body oval (Fig. 9), cephalothorax black, abdomen dark reddish brown and pterostigma black in life, wings flat in repose. For morphometric data see Table 1.

Mounted specimens.

Head, thorax, antennae, ultimate rostral segment, legs and genital plate brown, abdominal tergites VII–VIII with brown broad transverse bands, forewing veins and pterostigma brown, the other parts of body pale. Dorsum of head with sparse imbrications, tibiae, tarsi, venter of femora and abdominal tergites VI–VIII with dense spinulose imbrications. Spiracles oval, closed, on abdominal segments II–VI, spiracular plates brown. Dorsal setae of body short and pointed, on light brown seta-bearing sclerites. Head with 10–25 dorsal setae between antennae and 15–20 dorsal setae between eyes; pronotum with 1 pair of spinal, 1 pair of pleural and 2 pairs of marginal setae; mesonotum with 19–30 setae; abdominal tergite I with 5–8 spino-pleural and 1 pair of marginal setae; abdominal tergite II with 4–9 spino-pleural and 1 pair of marginal setae; abdominal tergite III with 6–8 spino-pleural and 1 pair of marginal setae; abdominal tergites IV–V each with 5–8 spino-pleural and 1 pair of marginal setae; abdominal tergites VI–VII each with 4–6 spino-pleural and 1 pair of marginal setae; tergite VIII with 5–8 setae. Cephalic setae, marginal setae on abdominal tergite I and spinal setae on tergite VIII 0.22–0.33 times, 0.29–0.53 times and 0.58–0.80 times as long as widest diameter of antennal segment III, respectively.

Head (Fig. 10): Front protuberant. Eyes compound. Antennae 5-segmented (Figs. 2, 11), with dense spinulose imbrications on segments III–V; 0.32–0.35 times as long as body. Length in proportion of segments I–V: 15 : 12 : 100 : 45 : 19+7, respectively. Processus terminalis 0.24–0.48 times as long as base of the segment V. Setae on antennae sparse. Segments I–V each with 1–3, 2, 0, 0, 0+0 setae, respectively. Processus terminalis with 5 apical setae. Primary rhinaria small, round and ciliated. Segments III, IV and base of segment V each with 37–44, 16–21, 6–9 annular secondary rhinaria, respectively. Rostrum short, not reaching mid-coxae. Ultimate rostral segment blunt wedge-shaped (Figs. 3, 12), 1.09–1.55 times as long as its basal width, 0.61–0.71 times as long as second hind tarsal segment; with 2 pairs of primary setae and 1 pair of accessory setae.

Thorax: Legs normal. Trochanters and femora fused. Hind trochanter and femur 1.21–1.48 times as long as antennal segment III, hind tibia 0.28–0.31 times as long as body. Setae on legs dense, fine and pointed. Setae on hind tibia 0.68–0.92 times as long as its mid-diameter. First tarsal chaetotaxy: 3, 3, 3. Dorso-apical setae on second hind tarsal segments expanded at apices. Empodial setae pointed, exceeding tip of claws. Fore wings (Figs. 4, 9) with pterostigma narrow and long, distal margin of pterostigma forming almost a straight line with the hind margin, media unbranched, not united with cubitus, and two cubitus veins fused at base; hind wings with 2 obliques.

Abdomen: Siphunculi absent. Cauda, anal plate and genital plate with dense spinulose imbrications. Cauda knobbed, distinctly constricted at base (Figs. 5, 13), 0.80–1.01 times as long as its basal width, with 12–19 setae. Anal plate bilobed (Figs. 6, 14), each with 10–15 setae. Genital plate broad round (Figs. 7, 15), with 39–52 setae. Two gonapophyses each with 3–9 short setae.

Specimens examined.

Holotype: alate viviparous female, CHINA: Hunan (Jishou City, 28°17'23"N, 109°43'11"E, altitude 240 m), 21 Apr. 2010, No. Y8974–1-8, on Distylium chinense, coll. X. T. Li (NZMCAS). Paratypes: 1 fundatrix and 11 alate viviparous females, with the same collection data as holotype.

Taxonomic notes.

The new species is similar to Indonipponaphis fulvicola Sorin, but differs from the latter as follows: Fundatrix: body larger, 2.036 mm long (the latter: about 1.250 mm long); first tarsal chaetotaxy: 2, 2, 2 (the latter: 3, 3, 2); siphunculi absent (the latter: present); cauda knobbed (the latter: round). Alatae from galls: base of antennal segment V with 6–9 secondary rhinaria (the latter: 11–14); abdomen with 5 pairs of spiracles (the latter: 4 pairs); first tarsal chaetotaxy: 3, 3, 3 (the latter: 3, 3, 2); media of fore wings unbranched (the latter: once branched); siphunculi absent (the latter: present); cauda knobbed (the latter: round).

Host plant.

Distylium chinense.

Biology.

The aphids live in galls on the upper side of leaves of Distylium chinense. In early March, small galls start to grow on young leaves, often rise from or near the midrib, spherical, pale green, sometimes with a pinkish tinge due to the dense soft hairs on the surface (Fig. 16). Usually one leaf bears only one gall. After about 30 days, the galls when fully developed are large, long, saccate, approximately 3.2 cm in length and 1.1 cm in diameter (Fig. 17). Later, they split at the tip, forming a flower-shaped opening (Figs. 19, 20), through which large honeydew droplets coated with much wax are expelled (Fig. 18). The galls are vase-shaped when mature (Fig. 20). The alate viviparous females mature in the galls in late April and fly to an unknown secondary host.

Figures 8–15.

Asiphonipponaphis vasigalla sp. n. Fundatrix 8 dorsal view of body. Alate viviparous female(emigrant from galls) 9 dorsal view of body 10 dorsal view of head 11 antenna 12 ultimate rostral segment 13 cauda 14 anal plate 15 genital plate. Scale bars = 0.10 mm.

Figures 16–20.

Galls of Asiphonipponaphis vasigalla sp. n. on Distylium chinense 16 small spherical gall on young leaf 17 large long saccate gall 18 large honeydew droplet coated with wax is being expelled through the opening 19 flower-shaped opening at the tip of gall 20 vase-shaped mature galls.

Acknowledgements

We gratefully thank X. T. Li for collecting, photographing the galls and providing biological information. We also thank F. D. Yang for specimen production. The work was supported by the National Natural Sciences Foundation of China (Nos. 30830017, 31061160186), National Science Funds for Distinguished Young Scientists (No. 31025024), National Science Fund for Fostering Talents in Basic Research (No. J0930004), and a grant (No. O529YX5105) from the Key Laboratory of the Zoological Systematics and Evolution of the Chinese Academy of Sciences.

References
Blackman RL, Eastop VF (1994) Aphids on the World’s Trees. An Identification and Information Guide. CAB International in Association with the Natural History Museum, Wallingford, 987 pp. http://www.aphidsonworldsplants.info [accessed 24.IV.2011]
Ghosh AK (1988) The Fauna of India and the Adjacent Countries (Homoptera: Aphidoidea) Part 4 Subfamilies: Phloemyzinae, Anoeciinae and Hormaphidinae. Zoological Survey of India, Calcutta, 429 pp.
Hille Ris Lambers D, Takahashi R (1959) Some species of Thoracaphis and of nearly related genera from Java (Homoptera, Aphididae). Tijdschrift Voor Entomologie 102: 1–16. http://biostor.org/reference/49728# [accessed 11.III.2011]
Matsumura S (1917) Synopsis of the Pemphigidae of Japan. In: Nagano K (Ed) A collection of Essays for Mr. Yasushi Nawa, Gifu, 39–94.
Monzen K (1934) Some contributions to the knowledges of the new and recorded species of the gall producing aphids. Bulletin of the Scientific Researches of the Alumni Association of the Morioka College of Agriculture and Forestry 9:13-34.
Monzen K (1954) Revision of some Japanese Hormaphidinae (Aphididae), with the descriptions of new genus and species. Annual Report of the Gakugei Faculty of the Iwate University 7: 46–60. http://ir.iwate-u.ac.jp/dspace/bitstream/10140/749/1/erar-v7n2p46–60.pdf [accessed 11.III.2011]
Noordam D (1991) Hormaphidinae from Java (Homoptera: Aphididae). Zoologische Verhandelingen 270:1-525.
Pergande T (1906) Description of two new genera and three new species of Aphididae. Entomological News 17: 205–210. http://biostor.org/reference/58031# [accessed 11.III.2011]
Sorin M (1987) The aphids causing galls on Distylium racemosum in Japan. In: Holman J, Pelikán J, Dixon AFG, Weismann L (Eds) Population structure, genetics and taxonomy of aphids and Thysanoptera. SPB Academic Publishing, The Hague, 219–223.
Sorin M (1996) Three new species and a new subspecies of Aphididae (Homoptera) causing galls on Distylium racemosum from Japan. Bulletin of Kogakkan University 35:235-260.
Sorin M (2003) Aphids on the planted trees (4). Shokubutsu Boeki 57: 480–483. (in Japanese)
Takahashi R (1958) Species of aphids causing galls on Distylium racemosum in Japan. Akitu 7:87-88.
Takahashi R (1962) Aphids causing galls on Distylium racemosum in Japan, with descriptions of two new related species (Aphididae, Homoptera). Bulletin of the University of Osaka Prefecture, Series B 13:1-11.