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FIGURE 7 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 7. SEM illustrations of structural features of protibia of Anillini, dorsal (E) and ventral (A–D, F–H) aspects: A– B—subtribe Nesamblyopina; A—Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Anillinus lescheni Sokolov and Carlton; D—Geocharidius comayaguanus Sokolov and Kavanaugh; E—Geocharidius zullini Vigna Taglianti; F—Zeanillus brouni Sokolov; G—Pelodiaetodes nunni Sokolov; H—Pelodiaetus sulcatipennis Jeannel. Legend: as—articulosetae; psr—posterior setal row. Scale = 0.05 mm.

FIGURE 20 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 20. Distributional records for the Nesamblyops species and images of male median lobe, obtained from specimens, collected in the line-connected with images localities. Green circles—N. solitarius; black circles—N. montanus; pink circles— N. rotundicollis; red circles—N. subrufus. Scale bar = 0.5 mm.

FIGURE 6 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 6. SEM illustrations of structural features of elytra of Anillini, left lateral aspect: A–B—subtribe Nesamblyopina; A—Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Anillinus carolinae Casey; D—Anillinus alleni Sokolov and Carlton; E—Serranillus donovani (Jeannel); F—Geocharidius jalapensis Sokolov and Kavanaugh; G—Zeanillus punctigerus (Broun); H—Pelodiaetodes nunni Sokolov; I—Pelodiaetus nunni Sokolov. Legend: ed2—scutellar seta; ed6— discal seta, ed8—apical seta; eo1…eo9—setae 1–9 of umbilical series of pores. Scale = 0.2 mm.

FIGURE 16 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 16. Line drawings of male genitalia of New Zealand Nesamblyops species. N. subrufus (Dublin Terrace, Upper Buller Gorge, Nelson, SO): A—left paramere, left lateral aspect, B—right paramere, right lateral aspect, C—median lobe, right lateral aspect. N. viator (Secretary Island, Grono Bay, Fjordland, SO): D—left paramere, left lateral aspect, E—right paramere, right lateral aspect, F—median lobe, right lateral aspect. N. victoriae (Capleston, Victoria Range, Buller, SO): G—left paramere, left lateral aspect, H—right paramere, right lateral aspect, I—median lobe, right lateral aspect. Scale bar = 0.1 mm.

FIGURE 5 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 5. Digital illustrations of structural features of pterothorax of Anillini, ventral aspect: A–D—subtribe Nesamblyopina; A—Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Nesamblyops brouni Sokolov; D—Nesamblyops viator n.sp.; E—Anillinus langdoni Sokolov and Carlton; F—Anillinus Cherokee Sokolov and Carlton; G—Geocharidius longinoi Sokolov and Kavanaugh; H—Geocharidius disjunctus Sokolov and Kavanaugh; I—Zapotecanillus longinoi Sokolov; J—Zeanillus pellucidus Sokolov; K—Zeanillus pallidus (Broun); L—Zeanillus nunni Sokolov; M—Pelodiaetodes insularis Sokolov; N—Pelodiaetodes nunni Sokolov; O—Pelodiaetodes moorei Sokolov; P—Pelodiaetus sulcatipennis Jeannel. Legend: mtes—metendosternite. Scales intentionally omitted.

FIGURE 4 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 4. SEM illustrations of structural features of pterothorax of Anillini, ventral aspect: A–B—subtribe Nesamblyopina; A—Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Anillinus lescheni Sokolov and Carlton; D— Anillinus forthoodensis Sokolov and Reddell; E—Geocharidius jalapensis Sokolov and Kavanaugh; F—Zeanillus pallidus (Broun); G—Pelodiaetodes insularis Sokolov; H—Pelodiaetodes nunni Sokolov; I—Pelodiaetus sulcatipennis Jeannel. Legend: mes—mesanepisternum, mscx—mesocoxa, msts—mesothoracic anapleural suture, msv—mesoventrite, mtcx— metacoxal, mtp—metaventral process, mtv—metaventrite. Scale = 0.1 mm.

FIGURE 9 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 9. Digital images of habitus of New Zealand Nesamblyops species, dorsal aspect. A—N. canaanensis (Canaan, Nelson, SO), B—N. disjunctus (Fletchers Creek, Buller, SO), C—N. hobbit (9mi. N Karamea, Nelson, SO), D—N. karamea (Karamea River Gorge, Nelson, SO), E—N. kuscheli (Flora Hut, Mount Arthur, Nelson, SO), F—N. magnificus (Allison Reserve, Akatore, Dunedin, SO). Scale bar = 1.0 mm.

FIGURE 23 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 23. Distributional records for the Nesamblyops species and images of male median lobe, obtained from specimens, collected in the line-connected with images localities. Black circles—N. viator; red circles—N. magnificus. Scale bar = 0.5 mm.

FIGURE 2 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 2. SEM illustrations of structural features of labial complex of Anillini: A–B—subtribe Nesamblyopina; A— Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Zeanillus punctigerus (Broun); D—Pelodiaetodes insularis Sokolov; E—Anillinus forthoodensis Sokolov and Reddell; F—Geocharidius minimus Sokolov and Kavanaugh. Legend: ca—cardo, bs—basistipes, bss—basal stipital setae, mss—medial stipital setae, pf—palpifer. Scale = 0.1 mm.

FIGURE 3 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 3. SEM illustrations of structural features of pronota of Anillini: A–B—subtribe Nesamblyopina; A—Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Anillinus alleni Sokolov and Carlton; D—Anillinus forthoodensis Sokolov and Reddell; E—Serranillus jeanneli Barr; F—Geocharidius balini Sokolov and Kavanaugh; G—Zeanillus punctigerus (Broun); H—Pelodiaetodes nunni Sokolov; I—Pelodiaetus nunni Sokolov. Legend: ast—setae of anterior margin of pronotum, bst—setae of basal margin of pronotum. Scale = 0.1 mm.

FIGURE 1 in Fourteen new species of the genus Nesamblyops Jeannel (Coleoptera: Carabidae: Anillini) from the South Island of New Zealand with redescription of the genus and description of a new subtribe

FIGURE 1. SEM illustrations of structural features of heads of Anillini: A–C—subtribe Nesamblyopina; A—Nesamblyops oreobius (Broun); B—Nesamblyops subcaecus (Sharp); C—Nesamblyops magnificus, n.sp.; D—Anillinus alleni Sokolov and Carlton; E—Anillinus acutipennis Sokolov and Reddell; F—Geocharidius jalapensis Sokolov and Kavanaugh; G—Zeanillus punctigerus (Broun); H—Pelodiaetodes nunni Sokolov; I—Pelodiaetus sulcatipennis Jeannel. Legend: cl—clypaeus, lse— lateral clypeal setula, mse—medial clypeal setula, om—ommatidium, trom—trace of disappeared ommatidium. Scale = 0.1 mm.

opennotspecifiedAug 2011View details →

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.

opennotspecifiedOct 2019View details →

Distribution. Might still occur on Big South Cape (= Taukihepa) I and neighboring Putauhina I or on privately owned islands off Stewart I, New Zealand. in Mystacinidae

Distribution. Might still occur on Big South Cape (= Taukihepa) I and neighboring Putauhina I or on privately owned islands off Stewart I, New Zealand.

opennotspecifiedAug 2011View details →

Distribution. Himalayas in N India (Jammu and Kashmir, Sikkim), Nepal, and W China (S Xizang). Introduced into New Zealand (South Island), South Africa (Western Cape), and California (USA). in Bovidae

Distribution. Himalayas in N India (Jammu and Kashmir, Sikkim), Nepal, and W China (S Xizang). Introduced into New Zealand (South Island), South Africa (Western Cape), and California (USA).

opennotspecifiedJul 2016View details →

Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms. in Leporidae

Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms.

FIGURES 13–15 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)

FIGURES 13–15. Eunomy (left corium), most frequently observed pigmentation patterns. (13) Kiwisaldula waiho, (14) K. butleri, (15) K. laelaps.

FIGURES 9–12 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)

FIGURES 9–12. Facial views of Kiwisaldula species; males. (9) K. waiho, (10) K. hurunui, (11) K. butleri, (12) K. laelaps.

FIGURES 5–8 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)

FIGURES 5–8. Dorsal views of type specimens with labels. Scale bar = 1 mm. (5–6) Kiwisaldula butleri, female holotype and labels, (7–8) K. laelaps, male lectotype and labels.

FIGURES 1–4 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)

FIGURES 1–4. Dorsal views of Kiwisaldula species (males; legs and antennae omitted). Scale bar = 1 mm. (1) K. waiho, (2) K. hurunui, (3) K. butleri, (4) K. laelaps.

FIGURES 16–23 in Kiwisaldula waiho and K. hurunui, two new species of Saldidae (Hemiptera: Heteroptera) from the South Island of New Zealand, with redescriptions of K. butleri (White) and K. laelaps (White)

FIGURES 16–23. Schematic view of male genitalia (16–19) Paramere, ventral view. (16) Kiwisaldula waiho (shaft base broken), (17) K. hurunui (shaft base broken), (18a–b) K. butleri, (19) K. laelaps. (20–23) Parandria, posterior view. (20) K. waiho, (21) K. hurunui, (22) K. butleri, (23) K. laelaps.