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Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
FIGURE 3 in Oreocharis hainanensis (Gesneriaceae), a new species from karst regions in Hainan Island, South China
FIGURE 3. Molecular phylogeny of Hainan Oreocharis taxa and 57 Oreocharis species, based on the combined chloroplast gene trnLtrnF and nuclear ribosomal DNA (nrDNA) sequence ITS1/2 data matrices. Posterior probability (PP) and Bootstrap value (BS) are showed above branches (only shown if BS> 50%). Hainan Oreocharis taxa were showed in grey.
FIGURE 1. Oreocharis hainanensis S.J.Ling & M.X in Oreocharis hainanensis (Gesneriaceae), a new species from karst regions in Hainan Island, South China
FIGURE 1. Oreocharis hainanensis S.J.Ling & M.X. Ren sp. nov. A. Habitat; B. habit; C. adaxial leaf surface; D. abaxial leaf surface; E. lateral view of corolla, sepal and calyx; F. face view of corolla; G. opening flower showing stamens and staminode; H. pistil, stamens and staminode; I. capsule; J. fruit pods; K. seeds; L–N. Main floral visitors: L. Braunapis sp.; M. Apis sp.; N. Amegilla sp.; All photos by Shao-Jun Ling.
FIGURE 2. Oreocharis hainanensis S.J.Ling & M.X in Oreocharis hainanensis (Gesneriaceae), a new species from karst regions in Hainan Island, South China
FIGURE 2. Oreocharis hainanensis S.J.Ling & M.X. Ren sp. nov. A. Habit; B. abaxial leaf surface; C. lateral view of corolla, sepal and calyx; D. front view of corolla; E. opening corolla showing stamens and staminode; F. pistil, stamens and staminode; G. capsule; H. seed. (Drawn by Shu-Ping Guan based on the holotype S.J.Ling 2020091701 in HUTB).
Subspecies and Distribution. F. s. silvestris Schreber, 1777 — Europe E to the Carpathian Mts and the River Dnieper N of the Black Sea. F.s. brockmani Pocock, 1944 — Somalia. F. s. cafra Desmarest, 1822 — Zimbabwe, S Mozambique and South Africa. F. s. caucasica Satunin, 1905 — Caucasus Mts and Turkey. F.s. caudata Gray, 1874 — deserts E Caspian Sea to NW China (Xinjiang) and Mongolia. F. s. foxi Pocock, 1944 — Senegal to Lake Chad. F.s. gordoni Harrison, 1968 — Batinah coast of Oman. F.s. grampia G. S. Miller, 1907 — N Scotland. F. s. griselda Thomas, 1926 — Kalahari region to S Angola. F. s. iraki Cheesman, 1920 — Arabian Desert regions. F. s. lybica Forster, 1780 — desert regions of N Africa to Sudan and N Niger. F.s. melland: Schwann, 1904 — SC Africa. F.s. nesterovi Biurla, 1916 — Mesopotamian region to SW Iran. F. s. ocreata Gmelin, 1791 — Ethiopian highlands. F. s. ornata Gray, 1830 — India. Probably W through Iran. F.s. pyrrhus Pocock, 1944 — N Angola and SW Zaire. F. s. sarda Lataste, 1885 — coastal Maghreb region of Morocco and Algeria. F.s. tristrami Pocock, 1944 — Palestine and Red Sea coast of Arabia. F.s. ugandae Schwann, 1904 — E Africa. in Felidae
Subspecies and Distribution. F. s. silvestris Schreber, 1777 — Europe E to the Carpathian Mts and the River Dnieper N of the Black Sea. F.s. brockmani Pocock, 1944 — Somalia. F. s. cafra Desmarest, 1822 — Zimbabwe, S Mozambique and South Africa. F. s. caucasica Satunin, 1905 — Caucasus Mts and Turkey. F.s. caudata Gray, 1874 — deserts E Caspian Sea to NW China (Xinjiang) and Mongolia. F. s. foxi Pocock, 1944 — Senegal to Lake Chad. F.s. gordoni Harrison, 1968 — Batinah coast of Oman. F.s. grampia G. S. Miller, 1907 — N Scotland. F. s. griselda Thomas, 1926 — Kalahari region to S Angola. F. s. iraki Cheesman, 1920 — Arabian Desert regions. F. s. lybica Forster, 1780 — desert regions of N Africa to Sudan and N Niger. F.s. melland: Schwann, 1904 — SC Africa. F.s. nesterovi Biurla, 1916 — Mesopotamian region to SW Iran. F. s. ocreata Gmelin, 1791 — Ethiopian highlands. F. s. ornata Gray, 1830 — India. Probably W through Iran. F.s. pyrrhus Pocock, 1944 — N Angola and SW Zaire. F. s. sarda Lataste, 1885 — coastal Maghreb region of Morocco and Algeria. F.s. tristrami Pocock, 1944 — Palestine and Red Sea coast of Arabia. F.s. ugandae Schwann, 1904 — E Africa.
Distribution. SW Russian Far East (Ussuri region), North and South Korea, Japan including many offshore Is (Tsushima, Yakushima, Tanegashima, Kuchinoshima, Takarajima, Amami-Oshima, Kakeroma-Jima, Tokunoshima, Okinawajima, Miyakojima, Irabu, Ishigakijima, Iriomotejima, and Yonagunijima), C, E & S China, Taiwan and Hainan Is, N Myanmar, N Laos, N & C Vietnam (including Cat Ba and Kaitien Is), and scattered records in NC, SC & NE India (Uttar Pradesh, Arunachal Pradesh, and Andhra Pradesh); there is a record from Sakhalin I, but this requires confirmation. in Vespertilionidae
Distribution. SW Russian Far East (Ussuri region), North and South Korea, Japan including many offshore Is (Tsushima, Yakushima, Tanegashima, Kuchinoshima, Takarajima, Amami-Oshima, Kakeroma-Jima, Tokunoshima, Okinawajima, Miyakojima, Irabu, Ishigakijima, Iriomotejima, and Yonagunijima), C, E & S China, Taiwan and Hainan Is, N Myanmar, N Laos, N & C Vietnam (including Cat Ba and Kaitien Is), and scattered records in NC, SC & NE India (Uttar Pradesh, Arunachal Pradesh, and Andhra Pradesh); there is a record from Sakhalin I, but this requires confirmation.
FIGURE 60 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 60. Distribution of Plecoptera in cities of Guangxi. a. Tyloperla bilobata Mo, Wang & Li, 2020. b. Tyloperla courtneyi Stark & Sivec, 2005. c. Tyloperla sinensis Yang & Yang, 1993. d. Cerconychia multiseta Mo, Liu & Li, 2021. e. Styloperla jiangxiensis Yang & Yang, 1990. f. Styloperla spinicercia Wu, 1935.
FIGURE 58 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 58. Distribution of Plecoptera in cities of Guangxi. a. Neoperlops gressitti Banks, 1939. b. Neoperlops triangulatus Mo, Wang, Li & Murányi, 2020. c. Paragnetina insignis Banks, 1939. d. Sinacroneuria obscura Li & Murányi, 2017. e. Sinacroneuria wui (Yang & Yang, 1998). f. Togoperla canilimbata (Enderlein, 1909).
FIGURE 57 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 57. Distribution of Plecoptera in cities of Guangxi. a. Neoperla truncata Wu, 1948. b. Neoperla wui Yang & Yang, 1990. c. Neoperla xuansongae Li & Li, 2013. d. Neoperla yao Stark, 1987. e. Neoperla yentu Cao & Bae, 2007. f. Neoperlops cheni (Wu, 1938).
FIGURE 56 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 56. Distribution of Plecoptera in cities of Guangxi. a. Neoperla shangsiensis Mo, Wang, Li & Murányi, 2021. b. Neoperla shiwandashana Mo, Yao, Wang & Li, 2019. c. Neoperla similidella Li & Wang, 2013. d. Neoperla similidelphina Mo, Li & Murányi, 2021. e. Neoperla tadpolata Li & Murányi, 2014. f. Neoperla transversprojecta Du & Sivec, 2004.
FIGURE 53 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 53. Distribution of Plecoptera in cities of Guangxi. a. Neoperla delphina Li, Mo & Wang, 2020. b. Neoperla falcatata Mo, Wang, Li & Murányi, 2021. c. Neoperla fanjingshana Yang & Yang, 1992. d. Neoperla furcostyla Li & Qin, 2013. e. Neoperla guangxiensis Du & Sivec, 2004. f. Neoperla henana Li, Wu & Zhang, 2011.
FIGURE 59 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 59. Distribution of Plecoptera in cities of Guangxi. a. Togoperla condyla Li & DeWalt, 2012. b. Togoperla noncoloris Du & Chou, 1999. c. Togoperla perpicta Klapálek, 1921. d. Togoperla totanigra Du & Chou, 1999. e. Togoperla triangulata Du & Chou, 1999. f. Togoperla tricolor Klapálek, 1921.
FIGURE 52 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 52. Distribution of Plecoptera in cities of Guangxi. a. Neoperla bicolor Yang, Zhang & Li, 2017. b. Neoperla bilineata Wu & Claassen, 1934. c. Neoperla cavaleriei (Navás, 1922). d. Neoperla chebalinga Chen & Du, 2016. e. Neoperla curvilobata Mo, Wang & Li, 2020. f. Neoperla curvispina Wu, 1948.
FIGURE 55 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 55. Distribution of Plecoptera in cities of Guangxi. a. Neoperla mesospina Li & Wang, 2013. b. Neoperla mnong Stark, 1987. c. Neoperla muranyii Yang, Zhang & Li, 2017. d. Neoperla pani Chen & Du, 2016. e. Neoperla quadrispina Li, Mo & Wang, 2020. f. Neoperla rotunda Wu, 1948.
FIGURE 51 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 51. Distribution of Plecoptera in cities of Guangxi. a. Kamimuria cheni Wu, 1948. b. Kamimuria extremispina Du, 2006. c. Kamimuria guangxia Li & Wang, 2013. d. Kamimuria longispina Wu, 1948. e. Kamimuria taoi Wu, 1936. f. Kamimuria tergistigma Du, 2004.
FIGURE 50 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 50. Distribution of Plecoptera in cities of Guangxi. a. Flavoperla retusata Mo, Li & Wang, 2021. b. Flavoperla yangi Mo, Li & Murányi, 2021. c. Furcaperla bifurcata (Wu, 1948). d. Furcaperla Cn-G. e. Hemacroneuria trilobata Mo, Wang & Li, 2020. f. Hemacroneuria violacea Enderlein, 1909.
FIGURE 48 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 48. Distribution of Plecoptera in cities of Guangxi. a. Nemoura tauripitis Mo, Li & Murányi, sp. nov. b. Sphaeronemoura acutispina Mo, Wang, Yang & Li, 2020. c. Cryptoperla teana Li & Murányi, 2018. d. Agnetina curvigladiata Du & Chou, 1998. e. Agnetina longihirta Du & Chou, 1998. f. Agnetina multispinosa (Wu, 1938).
FIGURE 47 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 47. Distribution of Plecoptera in cities of Guangxi. a. Indonemoura yangi Li & Yang, 2006. b. Nemoura alticalcaneum Mo, Wang & Li, sp. nov. c. Nemoura biplatta Zhao & Du, 2021. d. Nemoura cucurbitata Mo, Wang, Yang & Li, 2020. e. Nemoura ganeum Mo, Yang & Li, sp. nov. f. Nemoura perforata Li & Yang, 2006.
FIGURE 46 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 46. Distribution of Plecoptera in cities of Guangxi. a. Indonemoura furcoloba Li & Yang, 2017. b. Indonemoura maoershana Mo, Wang, Yang & Li, 2020. c. Indonemoura quadrata Mo, Wang, Yang, Li & Murányi, 2019. d. Indonemoura quadrispina Mo, Wang, Yang, Li & Murányi, 2019. e. Indonemoura scalprata (Li & Yang, 2007). f. Indonemoura voluta Li & Yang, 2008.
FIGURE 54 in Review and contribution to the stoneflies (Insecta: Plecoptera) of Guangxi Zhuang Autonomous Region, China, with new species and new records from South China
FIGURE 54. Distribution of Plecoptera in cities of Guangxi. a. Neoperla hubleyi Stark & Sivec, 2008. b. Neoperla infuscata Wu, 1935. c. Neoperla latispina Wang & Li, 2013. d. Neoperla leigongshana Du & Wang, 2007. e. Neoperla limbatella Navás, 1933. f. Neoperla lui Du, 2004.
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