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Research Article
Two new species of Encyrtidae (Hymenoptera, Chalcidoidea) from the eastern Pamir Plateau, with four new records from China
expand article infoOuyan Xi, Shuli Zhang§, Hongying Hu
‡ Xinjiang University, Urumqi, China
§ Kashi University, Kashi, China
Open Access

Abstract

Based on surveys of the superfamily Chalcidoidea (Hymenoptera) in the eastern part of Pamir Plateau from 2021 to 2023, 1770 specimens of Encyrtidae belonging to 21 species in 15 genera are identified and catalogued. Two new species, Acerophagus albuscorpus Xi & Hu, sp. nov. and Pseudectroma stemmatosteres Zhang & Hu, sp. nov., are described and illustrated. Four species, Ericydnus novosibiricus Sugonjaev & Gavrilyuk, 2012, Copidosoma charon Guerrieri & Noyes, 2005, Aphycus slavai Myartseva, 1981, and Trichomasthus marsus (Walker, 1837), are newly recorded from China, and their diagnoses and illustrations are provided.

Key words:

Acerophagus, Pseudectroma, taxonomy, alpine habitat, Xinjiang

Introduction

At present, two subfamilies, 518 known genera, and more than 4830 recognized species of Encyrtidae (Hymenoptera, Chalcidoidea) (Zhang et al. 2024) are known worldwide (UCD Community 2023; Universal Chalcidoidea Database Website. https://ucd.chalcid.org). In China, 483 species in 128 genera have been reported including 67 species in 34 genera from Xinjiang Uyhgur Autonomous Region (Zu et al. 2018; Kang et al. 2024). Most of encyrtids are primary endoparasitoids of various insects and other arthropods, but a few are hyperparasitoids (Trjapitzin 1989; Xu 1999; Zu et al. 2020). More than 400 species of Encyrtidae have been used worldwide as biological control agents against insect pests, some successfully (Hansen et al. 2012; Kapranas and Tena 2015). Species such as Psyllaephagus pilosus and P. bliteus have been successfully used for biological control of psylloids (Zou et al. 2023). Metaphycus Mercet are mainly primary endoparasitoids of Coccidae and Diaspididae (Hemiptera) (Tavares et al. 2019).

The Pamir Plateau, a mountain knot of the five major mountain systems in central Asia, forms the border between China and Tajikistan, Afghanistan, Pakistan, and other countries. The part on the southwestern edge of Xinjiang (36.7–39.8°N, 73.5–76.5°E), China, is commonly called the eastern (or East) Pamir Plateau. Most of the region lies at high altitude between 3300 and 6000 m above sea level (Wang et al. 2011). Its climate is characterized by a subcontinental to arid continental climate (Komatsu 2016), with average annual temperature about 3 °C with strong ultraviolet radiation. A variety of plants and insects from the Tibetan Plateau, Kashmir, Tian Shan, and Hindukush Mountain ranges converge here, and, thus, their types are complex (Nowak et al. 2022; Mętrak et al. 2023). Insects that can live in such an extreme environment need to be well adapted to it, and such environments are often represented by unique plateau species. However, records of species of Encyrtidae from such high-alpine environments are scarce worldwide and in China.

We collected specimens of Chalcidoidea in various habitats across the eastern Pamir’s main area between 2021 and 2023 using the line-transect method. After that, we carried out a more thorough taxonomic analysis of the Encyrtidae in the area using the morphometric categorization approach. We found two new species, Acerophagus albuscorpus Xi & Hu, sp. nov. and Pseudectroma stemmatosteres Zhang & Hu, sp. nov., which are desbribed here. We also found four newly recorded species in China: Ericydnus novosibiricus Sugonjaev & Gavrilyuk, 2012, Copidosoma charon Guerrieri & Noyes, 2005, Aphycus slavai Myartseva, 1981, and Trichomasthus marsus (Walker, 1837). Therefore, this study enriches the biodiverisity of the family Encyrtidae in the eastern Pamir and provides a reference for the application of native parasitic wasps in the Pamir Plateau.

Materials and methods

Specimens were collected in yellow pan traps or by sweeping with a net in Atushi City, Aketao County, Wuqia County, and Tashkurgan Tajik Autonomous County, Xinjiang, China, from 2021 to 2023. Collected specimens were preserved in 99% ethanol at −20 °C (Noyes 1982). Alcohol-soaked specimens were measured under a Nikon SMZ-745T stereomicroscope and photographed with a Nikon D7000 digital camera connected to the Nikon SMZ-25 stereomicroscope. Slide-mounted specimens were examined and photographed using a Nikon Ci3 microscope. All the studied specimens were preserved in the Insect Collection of the College of Life Science and Technology, Xinjiang University, Urumqi, Xinjiang, China (ICXU).

Morphological terminology follows that of Noyes and Hayat (1984), Gibson et al. (1997), Trjapitzin (1989), Zhang and Huang (2004), Noyes (2010). Absolute measurements were used for body length (not including the exserted part of the ovipositor), while relative measurements were used for other dimensions. The following abbreviations are used: POL = minimum distance between the posterior ocelli; OOL = minimum distance between posterior ocellus and eye margin; AOL = minimum distance between posterior ocellus and anterior ocellus; OCL = minimum distance between posterior ocellus and occipital margin; F1–F6 = funicle segments 1–6; Gt1–7 = gastral terga 1–7.

Results

Species of Encyrtidae in the eastern Pamir Plateau

We obtained 1770 specimens of Encyrtidae and identified them using the keys of Trjapitzin (1989) and Noyes (2010). We recognized 15 genera and 21 species, including two new species to science, and four newly recorded species from China (Table 1). The results show that Copidosoma Ratzeburg, 1844 had the most specimens collected; Copidosoma truncatellum accounted for 79% of all specimens.

Table 1.

Catalogue of Encyrtidae in the eastern Pamir Plateau, Xinjiang, China.

Subfamily Genus and species Distribution Number
Encyrtinae Acerophagus albuscorpus Xi & Hu, sp. nov. China (Xinjiang) 4
Aphycus slavai Myartseva, 1981 * Turkmenistan, China (Xinjiang) 11
Blastothrix britannica Girault, 1917 Palearctic, Nearctic regions 19
Cerchysius subplanus Dalman,1820 Palearctic, Oriental regions 4
Copidosoma agrotis (Fonscolombe, 1832) Palearctic region 156
Copidosoma aretas (Walker, 1838) Palearctic region 13
Copidosoma charon Guerrieri & Noyes, 2005 * Austria, Bosnia, Herzegovina, Czech Republic, UK (England), Finland, France, Norway, Spain, Sweden, China (Xinjiang) 6
Copidosoma truncatellum (Dalman,1820) Worldwide 1403
Copidosoma sp. 56
Discodes kryzhanovskii Myartseva, 1981 Turkmenistan, Uzbekistan, China 10
Pseudectroma stemmatosteres Zhang & Hu, sp. nov. China (Xinjiang) 10
Stemmatosteres muztagataensis Zhang & Hu, 2023 China (Xinjiang) 4
Syrphophagus arundinicola Hoffer, 1965 Armenia, Bulgaria, former Czechoslovakia, Italy, Moldova, Netherlands, Russia, China 9
Trichomasthus marsus (Walker, 1837) * UK (England), Germany, Norway, China (Xinjiang) 8
Tetracneminae Anagyrus matritensis Mercet, 1921 Croatia, former Czechoslovakia, Iran, Azerbaijan (Nakhichevan), Spain, Tunisia, China 19
Charitopus fulviventris Förster, 1860 Palearctic, Oriental, Neotropical regions 5
Ericydnus liaoi Liu, Wang & Li, 2013 China (Inner Mongolia, Xinjiang) 9
Ericydnus novosibiricus Sugonjaev & Gavrilyuk, 2012* Russia (Novosibirsk), China (Xinjiang) 8
Ericydnus ventralis (Dalman, 1820) Palearctic region 9
Leptomastix histrio (Förster, 1856) Germany, China 3
Rhopus hanni Zu & Li, 2020 China (Xinjiang, Tibet) 4

Descriptions of the two new species

Acerophagus albuscorpus Xi & Hu, sp. nov.

Fig. 1

Type material.

Holotype • ♀, in alcohol; China, Xinjiang, Tashkurgan Tajik Autonomous County, Kokyar Kirghiz Township, 38°7'50.7864"N, 74°58'39.018"E, altitude: 3565 m, 24. VII. 2021. Coll. Hu Hongying’ s insect research team by sweeping. Paratypes • 1 ♀ on slides, 2 ♀♀ in alcohol, same data as the holotype (all deposited in ICXU).

Figure 1. 

Acerophagus albuscorpus Xi & Hu, sp. nov., holotype female A dorsal habitus B fore wing C lateral habitus D mesosoma and metasoma in dorsal view E antenna F head and mesosoma in dorsal view G gaster in lateral view.

Description.

Female (holotype). Body. Length 1.04 mm; creamy white with multiple gray-brown spots except head, eyes blackish brown, ocelli white with red outline, antenna white with more or less brown margins on all segments except for F1, F2 and clava; pronotum with trapezoidal, gray-brown patch; mesoscutum and axilla yellowish, slightly glossy; scutellum mostly gray-brown; fore wing hyaline; the bases of femora, tibiae and all tarsi of hind legs slightly blackish brown; gaster with grayish-brown transverse band at base of Gt1, middle, and sides of Gt2–7; ovipositor yellowish brown, except base and tip brown.

Head. Dorsal length about half of head width; frontovertex 0.5× head width; occipital margin sharp; ocellus with apical angle obtuse, AOL: OOL: OCL = 3:3.1:2; eye height 1.2× malar space, width slightly equal to gena length. Antennal toruli below the eye lower margin; scape slightly subcylindrical, 4× as long as wide; pedicel slightly conic, short than funicle; F1–5 broader than long, each gradually widen; clava three segments, 3.5× as long as wide and 1.5× as long as funicle. Measurements (μm): head width, 27; frontovertex, 14.5; AOL, 3; OOL, 3.1; OCL, 2; eye length, 29; malar space, 10; gena length, 8; scape length and width, 14 and 3.5; pedicel length, 6; funicle length, 9; clava length and width, 14 and 4.

Mesosoma . Mesoscutum slightly swollen, straight posteriorly, about 0.6× as long as wide; axillae large and slightly separated in the middle; scutellum about as long as wide; fore wing strongly reduced, very short and small, about 0.8× as long as broad, not reaching base of gaster; mesotibial spur 0.7× mesotibia length. Measurements (μm): mesosoma length, 28; mesoscutum length, 18; scutellum length and width, 12 and 12; mesotibial spur length, 8; mesotibia length, 22.8; mesobasitarsus length, 8; fore wing length and width, 14.4 and 11.1.

Metasoma. Metasoma slightly < 1.8× mesosoma length; ovipositor exserted, its full length 1.5× as long as mid tibia and 0.7× as long as metasoma. Measurements (μm): metasoma length, 49; ovipositor length, 35.

Variation (female paratypes). Body length 0.84–1.04 mm; eye 1.2–1.3× as long as malar space; antennal clava 3.0–3.5× as long as wide.

Male. Unknown.

Etymology.

The name of the new species is derived from the Latin words albus, “white”, and corpus, “body”, and refers to the body color.

Comments.

The new species belongs to Acerophagus Smith, 1880. The new species is more similar to Acerophagus ovaliclavus Zu & Li, 2016. However, it differs from A. ovaliclavus in the following: frontovertex about 0.5× head wide, scape about 4× as long as broad, clava about 3.5× as long as broad, forewing brachypterous, all gastral terga with grayish-brown transverse bands, ovipositor about 1.5× as long as mid tibia in A. ovaliclavus: frontovertex 0.4× head wide, scape about 3.4× as long as broad and clava about 1.6×, forewing normal, only Gt5–7 with grayish-brown transverse bands, ovipositor 1.9× as long as mid tibia (Zu and Li 2017; Hu et al. 2019).

Pseudectroma stemmatosteres Zhang & Hu, sp. nov.

Figs 2, 3

Type material.

Holotype • ♀ card mounted, China, Xinjiang, Tashkurgan Tajik Autonomous County, Kokyar Kirghiz Township. 37°44'2.418"N, 75°15'23.4648"E, altitude: 3086 m, 22. VII. 2022. Coll. Hu Hongying’s insect research team by yellow pan trapping. Paratypes • 4 ♀♀, 5 ♂♂, same data as the holotype (all deposited in ICXU).

Figure 2. 

Pseudectroma stemmatosteres Zhang & Hu, sp. nov., holotype female A lateral habitus B antenna C head in ventral view and antennae D mesosoma and metasoma in dorsal view E head in frontal view and antennae F habitus in ventral view G hind leg.

Description.

Female (holotype). Body. Length 0.76 mm; yellow, except head orange, eye greyish black, antenna yellowish; mesosoma alutaceous, legs yellow with telotarsus brown; gaster yellowish except ovipositor terminal yellow brown.

Figure 3. 

Pseudectroma stemmatosteres Zhang & Hu, sp. nov., paratype male A habitus in dorsal view B antenna C head in frontal view D mesosoma and gaster in dorsal view.

Head. In frontal view, about 1.1× as wide as high and with extremely shallow scaly reticulations; frontovertex about 0.8× head width; in dorsal view, occipital margin bluntly rounded, with posterior margin concave forward; ocelli absent; eyes small, 0.6× head high; toruli below lower margin of eyes and about 0.8× as long as wide. Antenna with scape 3.7× as long as wide and about 0.9× frontovertex width; pedicel about equal to F1–4 combined; all funicle segments transverse, gradually increasing from F1–5; clava 2-segmented, slightly longer than scape and 2.8× as long as wide; mandible tridentate. Measurements (μm): head dorsal width and height, 25 and 22; frontovertex, 13; eye length, 13; antennal scape length and width, 11 and 3; pedicel length and width, 5 and 2.2; funicle length, 8; clava length and width, 11 and 4.

Mesosoma. Pronotum slightly longer than mesoscutum; mesoscutum transverse, 0.37× as long as wide; axilla not separated; scutellum 0.58× as length as width; wings absent; mesotibial spur 0.8× of mesobasitarsus length and 0.3× of mesotibial length. Measurements (μm): pronotum length, 9; mesosoma length, 26; mesoscutum length and width, 7 and 19; scutellum length and width, 7 and 12; mesotibial spur length, 5; mesotibia length, 20; mesobasitarsus length, 6.

Metasoma about 1.9× as long as mesosoma; hypopygium extending almost to apex of gaster; ovipositor exsertedabout 0.6× as long as gaster or 1.5× as long as mesotibia. Gt5 with three long setae on each side. Measurements (μm): metasoma length, 50; ovipositor length, 30.

Variation (female paratypes). Body length, 0.75–0.87 mm; head in frontal view almost 0.9× as broad as high; frontovertex about 0.5× head wide; eye length 0.5–0.6× as long as head height; metasoma 0.3–0.4× as long as wide.

Male. Body length 0.64–0.84 mm (Fig. 3). Generally similar to female except for antenna clava longer than female, male clava 3.4× as long as wide. Metasoma nearly round, about 1.1× as long as wide. Other characteristics similar to those in females.

Host.

Unknown.

Etymology.

The new species name is derived from stemma refers to ocelli.

Comments.

In Pseudectroma Girault, 1915, 13 species were previously known, but this new species differs from all of these. This new species is most similar to P. caribe Noyes, 2010, from which it differs in having the frontovertex about 0.5× the head wide, the occipital margin bluntly rounded, and the ovipositor 1.5× as long as the mesotibia; in P. caribe, the frontovertex is about 0.4× the head wide, the occipital margin is acute, and the ovipositor is about 2.0× as long as the mesotibia (Noyes 2010).

Species newly recorded from China

Ericydnus novosibiricus Sugonjaev & Gavrilyuk, 2012

Fig. 4

Ericydnus novosibiricus Sugonjaev & Gavrilyuk, 2012: 160–163.

Material examined.

China, Xinjiang • 5 ♀♀, Tashkurgan Tajik Autonomous County, Wahanzoulang, 37°7'57.59"N, 75°7'5.6892"E, altitude: 3826 m, 23.VII.2021. China, Xinjiang • 3 ♂♂, Dabudaer township, 38°7'50.7864"N, 74°58'39.018"E, altitude: 3566 m, 24.VII.2021. Coll. Hong-Ying Hu group, by sweeping (all deposited in ICXU).

Figure 4. 

Ericydnus novosibiricus Sugonjaev & Gavrilyuk, female A head in frontal view and antennae B fore wing C mesosoma in dorsal view D middle leg E gaster in dorsal view F dorsal habitus G mesosoma and metasoma in lateral view H lateral habitus.

Diagnosis.

Female. Body length about 1.7 mm; body black with blue-green metallic sheen. Eye deep reddish brown; gena with purple metallic luster; antenna and tegula black. Head 1.1× as wide as high; frontovertex about 0.4× head wide, with dense punctuations. Antenna with scape 6.5× as long as wide; pedicel 1.8× as long as wide, slightly shorter than F1; F1–6 slightly longer than wide; clava 3.2× as long as wide. Mesosoma with many rows of white setae; mesoscutum with scaly reticulation, 0.5× as long as wide. Fore wing short, 3.2× as long as wide, only reaching the basal 1/3 of gaster, metasoma longer than mesosoma; hypopygium extending to apex of gaster.

Male. Unknown.

Host.

Unknown.

Distribution.

China (Xinjiang); Russia (Novosibirsk).

Comments.

This newly collected specimens match the original description of E. novosibiricus (Sugonyaev and Gavrilyuk 2012). However, there are some differences: female body length about 1.7 mm (1.5–1.6 mm in original description); fore wing short and only reaching the basal 1/3 of gaster (considerably not reaching apex of abdomen, but approximately reaching level of pygostyli in original description). Nevertheless, we are confident our specimens are conspecific with E. novosibiricus.

Copidosoma charon Guerrieri & Noyes, 2005

Fig. 5

Copidosoma charon Guerrieri & Noyes, 2005: 146.

Material examined.

China, Xinjiang • 2 ♀♀, Kizilsu Kirgiz Autonomous Prefecture, Wuqia County, 40°15'6.244"N, 75°29'6.7308"E, altitude: 2765 m, 18.VII. 2021. Coll. Hong-Ying Hu group, by sweeping; China, Xinjiang • 4 ♀♀, Tashkurgan Tajik Autonomous County, Seritashike ranches, 37°25'4.0152"N, 75°22'13.9512"E, altitude: 3394 m, 23.VII.2021. Coll. Jin-Zhe Li, by sweeping (all deposited in ICXU).

Figure 5. 

Copidosoma charon Guerrieri & Noyes, 2005 female A antenna B head in frontal view C forewing D dorsal habitus E lateral habitus.

Diagnosis.

Female. Body length about 1.8 mm; body with blue-green metallic sheen; antennal scape with black metallic sheen, pedicel and flagellum brown. Frontovertex about 0.5× head width; malar space almost 0.7× as long as eye, slightly shorter than eye width. Antenna scape elongated, about 9.8–10.2× as long as wide, funicle 6-segmented, clava 3-segmented, about 5.5–6.1× as long as wide. Mesoscutum with regular, elongated sculpture; fore wing slender, 2.3× as long as wide; mesotibial spur 0.9× of mesobasitarsus length and about 0.25× of mesotibia length. Metasoma and mesosoma almost equal in length; hypopygium extending to apex of gaster; ovipositor about 0.2× as long as gaster.

Male. Unknown.

Host.

Unknown.

Distribution.

China (Xinjiang); Austria, Bosnia and Herzegovina, Czech Republic, UK (England), Finland, France, Spain, Sweden.

Comments.

Our specimens conform to original description of C. charon except for some minor differences: antenna scape more elongate, about 9.8× as long as wide, (7.5× as long as wide in the original description); fore wing 2.3× as long as wide (about 2.5 as long as broad in original description). We are convinced that our specimens are conspecific with C. charon (Guerrieri and Noyes 2005).

Trichomasthus marsus (Walker, 1837)

Fig. 6

Encyrtus marsus Walker, 1837: 444.

Trichomasthus marsus: Graham 1959: 147–175.

Material examined.

China, Xinjiang • 8 ♀♀, Kizilsu Kirgiz Autonomous Prefecture, Aketao County, 38°22'27.876"N, 74°59'54.0312"E, altitude: 3664 m, 19. VII. 2021. Coll. Hong-Ying Hu group, by sweeping (all deposited in ICXU).

Figure 6. 

Trichomasthus marsus, female A head in dorsal view B head in ventral view C mesosoma in dorsal view D fore wing E hypopygium F dorsal habitus G dorsolateral habitus H gaster in lateral view.

Diagnosis.

Female. Body length 1.1–1.3 mm; head dark brown with slightly metallic sheen; antenna with scape black, funicle yellowish brown, clava blackish brown. Mesonotum with blue-green strong metallic tinge; axilla and scutellum dark brown; fore and mid legs yellow and hind leg black. Frontovertex at most 1/3 head wide; scape slender, about 5× as long as wide; pedicel slightly longer than F1; pronotum and mesoscutum with reticulate sculpture. Fore wing hyaline, 1.8× as long as wide, marginal vein 3× as long as wide, marginal vein as long as postmarginal vein; stigma vein slightly elongated; stigma vein slightly longer than postmarginal vein. Gaster triangular and about equal to mesonotum length, hypopygium extending to middle of gaster.

Male. Unknown.

Host.

Unknown.

Distribution.

China (Xinjiang); Germany, Norway, United Kingdom.

Comments.

Our newly recorded female specimen matches the original description of T. marsus (Jensen and Sharkov 1989). However, it differs in the following: funicle yellowish brown and clava blackish brown (both funicle and clava blackish brown in original description); stigma vein slightly longer than postmarginal vein (stigma vein as long as postmarginal vein in original description). The other characteristics are consistent with the original description.

Aphycus slavai Myartseva, 1981

Fig. 7

Aphycus slavai Myartseva, 1981d: 20–21.

Aphycus slavai Myartseva: Japoshvili 2016: 3; Japoshvili 2017a: 3.

Material examined.

China, Xinjiang • 8 ♀♀, 3 ♂♂, Tashkurgan Tajik Autonomous County, Kashgar, 38°7'50.7864"N, 74°58'39.018"E, altitude: 3566 m, 24. VII. 2021. Coll. Hong-Ying Hu group, by sweeping (all deposited in ICXU).

Diagnosis.

Female. Body length about 1.1 mm; body dark brown, except head yellow, mesosoma yellow with dark-brown bands, densely covered with white bristles; antennae and legs light brown; fore wing hyaline with brown spots. Head about 0.9–1.0× as wide as high; frontovertex about 0.3× head wide; ocelli arranged in an equilateral triangle; OOL equal to OCL. Antenna inserted significantly below lower ocular line; scape nearly cylindrical, 7.1× as long as wide; pedicel 2.6× as long as wide; F1–4 transverse, F5 and F6 almost square. Mesoscutum about 0.7× as long as wide, with shallow reticulation; scutellum almost as long as wide; fore wing about 2.4× as long as wide; marginal vein absent; postmarginal vein short and about 0.3× as long as stigma vein; mesotibial spur shorter than mesobasitarsus. Hypopygium slightly extending from apex of gaster.

Male. Mostly similar to female except pedicel relatively shorter and clava unsegment; body paler (Fig. 7G).

Figure 7. 

Aphycus slavai A–F female A lateral habitus B head in dorsal view C head in lateral view D fore wing E antenna F gaster in dorsolateral view G male, lateral habitus.

Host.

Phenacoccus persimplex Borchsenius, 1949 (Hemiptera, Pseudococcidae) (Trjapitzin 1989; Japoshvili et al. 2016).

Distribution.

China (Xinjiang); Turkmenistan.

Comments.

This species is very similar to A. sulamanidzei, but the main difference is in the color of the abdomen; in A. sulamanidzei the entire abdomen is yellow. Our specimen matches the characteristics of A. slavai in having a dark-brown abdomen. Other characteristics are consistent with the original description of A. slavai (Myartseva 1981).

Discussion

We surveyed the eastern Pamir Plateau for three years, both in core areas and at higher elevations with diverse habitat types. We found 15 genera and 21 species. These taxa are likely to be better adapted to alpine environments.

This study primarily adds to our knowledge of the biodiversity of the family Encyrtidae on the eastern Pamir Plateau. Two new species of encyrtids are identified and essential data are provided for the biological management of agroforestry pests in alpine environments and the protection of natural pest insects. Copidosoma truncatellum was most abundant species found and was mostly distributed in Aktao and Wuqia counties. However, we used net-scanning to collect specimens, so very little information was gathered on the hosts of the species found. In the future, we aim to collect hosts and perform lab rearing to clarify hosts. For the two new species, few specimens were collected, and we will try to collect additional material.

Acknowledgements

We thank Jinzhe Li for helping with collecting specimens, planning, and staff coordination in the protected areas. Specimen identification process was guided and advised by Yanzhou Zhang (Institute of Zoology, Chinese Academy of Sciences, Beijing, China). Many thanks to Serguei V. Triapitsyn (University of California) for comments on the manuscript and for revision of the English.

Additional information

Conflict of interest

The authors have declared that no competing interests exist.

Ethical statement

No ethical statement was reported.

Funding

This project was supported by National Natural Science Foundation of China (32070472).

Author contributions

Conceptualization: OX, SZ. Data curation: OX, SZ. Formal analysis: HH. Funding acquisition: HH. Investigation: SZ, OX, HH. Methodology: SZ, OX, HH. Project administration: HH. Writing-original draft: OX.

Author ORCIDs

Ouyan Xi https://orcid.org/0009-0002-7039-5952

Hongying Hu https://orcid.org/0000-0002-2295-1072

Data availability

All of the data that support the findings of this study are available in the main text.

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Ouyan Xi and Shuli Zhang contributed equally to this work.
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