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Aethomys silindensis was previously listed as a subspecies of A. chrysophilus. Monotypic. Distribution. Eastern Highlands of Zimba- bwe and neighboring W Mozambique. in Muridae

Aethomys silindensis was previously listed as a subspecies of A. chrysophilus. Monotypic. Distribution. Eastern Highlands of Zimba- bwe and neighboring W Mozambique.

Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae

Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).

The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996). in Muridae

The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996).

Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996). in Muridae

Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996).

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Ubergraph edge list

<p>Normalized edge list of Ubergraph using bioregistry</p>

FIGURES 182‒189. Habitus. 182. Trioza nigra, fifth instar immature. 183. Trioza quercicola, adult male. 184. Trioza quercicola, adult female. 185. Trichochermes rhamnisugus, adult female. 186. Trichochermes rhamnisugus, fifth instar immature. 187. Heterotrioza stackelbergi, adult male. 188. Heterotrioza stackelbergi, adult female. 189 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 182‒189. Habitus. 182. Trioza nigra, fifth instar immature. 183. Trioza quercicola, adult male. 184. Trioza quercicola, adult female. 185. Trichochermes rhamnisugus, adult female. 186. Trichochermes rhamnisugus, fifth instar immature. 187. Heterotrioza stackelbergi, adult male. 188. Heterotrioza stackelbergi, adult female. 189. Enclosed gall of Heterotrioza stackelbergi. (Photos 183–184, 187–189 from Cho et al. (2017a))

FIGURES 86‒93. Habitus. 86. Cacopsylla elaeagni, adult male. 87. Cacopsylla elaeagni, adult female. 88. Cacopsylla elaeagni, fifth instar immature. 89. Cacopsylla elaeagnicola, adult male. 90. Cacopsylla elaeagnicola, teneral adult female. 91. Cacopsylla fatsiae, adult male. 92. Cacopsylla fatsiae, teneral adult female. 93 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 86‒93. Habitus. 86. Cacopsylla elaeagni, adult male. 87. Cacopsylla elaeagni, adult female. 88. Cacopsylla elaeagni, fifth instar immature. 89. Cacopsylla elaeagnicola, adult male. 90. Cacopsylla elaeagnicola, teneral adult female. 91. Cacopsylla fatsiae, adult male. 92. Cacopsylla fatsiae, teneral adult female. 93. Cacopsylla fatsiae, fifth instar immatures.

FIGURES 54‒61. Habitus. 54. Acizzia sasakii, adult male. 55. Acizzia sasakii, adult female. 56. Colophorina flaveola, adult male. 57. Colophorina robinae, adult male. 58. Colophorina robinae, adult female. 59. Colophorina robinae, fifth instar immature. 60. Epiacizzia kuwayamai, adult male. 61 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 54‒61. Habitus. 54. Acizzia sasakii, adult male. 55. Acizzia sasakii, adult female. 56. Colophorina flaveola, adult male. 57. Colophorina robinae, adult male. 58. Colophorina robinae, adult female. 59. Colophorina robinae, fifth instar immature. 60. Epiacizzia kuwayamai, adult male. 61. Epiacizzia kuwayamai, adult female. (Photos 56–61 from Cho et al. (2017a))

FIGURES 150‒157. Habitus. 150. Bactericera gobica, adult male. 151. Bactericera gobica, adult female. 152. Bactericera koreostriola, adult male. 153. Bactericera koreostriola, adult female. 154. Bactericera myohyangi, adult female. 155. Bactericera yamagishii, adult male. 156. Bactericera yamagishii, adult female. 157 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 150‒157. Habitus. 150. Bactericera gobica, adult male. 151. Bactericera gobica, adult female. 152. Bactericera koreostriola, adult male. 153. Bactericera koreostriola, adult female. 154. Bactericera myohyangi, adult female. 155. Bactericera yamagishii, adult male. 156. Bactericera yamagishii, adult female. 157. Eotrioza ussuriensis, adult male. (Photos 150–151 from Cho et al. (2016a), 157 from Cho et al. (2017a))

FIGURES 142‒149. Habitus. 142. Psylla alniformosanaesuga, adult female. 143. Psylla alniformosanaesuga, fifth instar immature. 144. Spanioneura longicauda, teneral adult male. 145. Spanioneura longicauda, adult female. 146. Spanioneura longicauda, fifth instar immature. 147. Bactericera calcarata, adult male. 148. Bactericera distinctissima, adult male. 149 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 142‒149. Habitus. 142. Psylla alniformosanaesuga, adult female. 143. Psylla alniformosanaesuga, fifth instar immature. 144. Spanioneura longicauda, teneral adult male. 145. Spanioneura longicauda, adult female. 146. Spanioneura longicauda, fifth instar immature. 147. Bactericera calcarata, adult male. 148. Bactericera distinctissima, adult male. 149. Bactericera distinctissima, adult female. (Photos 142–146 from Cho et al. (2017a))

FIGURES 30‒37. Habitus. 30. Calophya shinjii, adult female. 31. Calophya shinjii, fifth instar immatures. 32. Calophya verticornis, adult male. 33. Calophya verticornis, adult female. 34. Carsidara limbata, adult male. 35. Carsidara limbata, adult female. 36. Carsidara limbata, fifth instar immature. 37 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 30‒37. Habitus. 30. Calophya shinjii, adult female. 31. Calophya shinjii, fifth instar immatures. 32. Calophya verticornis, adult male. 33. Calophya verticornis, adult female. 34. Carsidara limbata, adult male. 35. Carsidara limbata, adult female. 36. Carsidara limbata, fifth instar immature. 37. Homotoma unifasciata, adult male. (Photos 34–36 from Cho et al. (2016b), 37 from Cho et al. (2017a))

FIGURES 14‒21. Habitus. 14. Craspedolepta yongjungi, fifth instar immature. 15. Rhodochlanis suaedicola, adult male. 16. Rhodochlanis suaedicola, adult female. 17. Rhodochlanis suaedicola, fifth instar immature. 18. Rhusaphalara minimia, adult male. 19. Rhusaphalara minimia, adult female. 20. Rhusaphalara minimia, fifth instar immature. 21 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 14‒21. Habitus. 14. Craspedolepta yongjungi, fifth instar immature. 15. Rhodochlanis suaedicola, adult male. 16. Rhodochlanis suaedicola, adult female. 17. Rhodochlanis suaedicola, fifth instar immature. 18. Rhusaphalara minimia, adult male. 19. Rhusaphalara minimia, adult female. 20. Rhusaphalara minimia, fifth instar immature. 21. Calophya nigra, teneral adult male. (Photo 14 from Cho et al. (2017a))

FIGURES 6‒13. Habitus. 6. Aphalara avicularis, adult male. 7. Aphalara fasciata, adult male. 8. Aphalara freji, adult male. 9. Aphalara jungsukae, adult male. 10. Craspedolepta formosa, adult male. 11. Craspedolepta formosa, adult female. 12. Craspedolepta yongjungi, adult male. 13 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 6‒13. Habitus. 6. Aphalara avicularis, adult male. 7. Aphalara fasciata, adult male. 8. Aphalara freji, adult male. 9. Aphalara jungsukae, adult male. 10. Craspedolepta formosa, adult male. 11. Craspedolepta formosa, adult female. 12. Craspedolepta yongjungi, adult male. 13. Craspedolepta yongjungi, adult female. (Photos 6, 8, 10–13 from Cho et al. (2017a))

FIGURES 46‒53. Habitus. 46. Syringilla humerosa, adult female. 47. Syringilla humerosa, fifth instar immatures. 48 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 46‒53. Habitus. 46. Syringilla humerosa, adult female. 47. Syringilla humerosa, fifth instar immatures. 48. Egg mass of Syringilla humerosa. 49. Livia khaziensis, adult male. 50. Syntomoza magna, adult male. 51. Acizzia jamatonica, adult male winter form. 52. Acizzia jamatonica, adult female summer form. 53. Acizzia jamatonica, fifth instar immature. (Photo 49 from Cho et al. (2017a))

FIGURES 110‒117. Habitus. 110. Cacopsylla moiwasana, adult female. 111. Cacopsylla nigella, adult male. 112. Cacopsylla nigella, adult female. 113 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 110‒117. Habitus. 110. Cacopsylla moiwasana, adult female. 111. Cacopsylla nigella, adult male. 112. Cacopsylla nigella, adult female. 113. Cacopsylla nigella, overwintering second and third instar immatures. 114. Cacopsylla nigella, fifth instar immature. 115. Cacopsylla nopeunsanicola, adult male. 116. Cacopsylla nopeunsanicola, adult female. 117. Cacopsylla nopeunsanicola, fifth instar immature. (Photos 110 from Cho et al. (2019a), 111, 114 from Cho et al. (2017b), 115–117 from Cho et al. (2017a))

FIGURES 174‒181. Habitus. 174. Trioza cinnamomi, adult female. 175. Trioza cinnamomi, fifth instar immature. 176 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 174‒181. Habitus. 174. Trioza cinnamomi, adult female. 175. Trioza cinnamomi, fifth instar immature. 176. Pit galls of Trioza cinnamomi. 177. Trioza machilicola, adult female. 178. Fifth instar immature mummy of Trioza machilicola. 179. Pit galls and symtom of Trioza machilicola. 180. Trioza nigra, adult male. 181. Trioza nigra, adult female. (Photos 174–179 from Cho et al. (2017a))

FIGURES 78‒85. Habitus. 78. Cacopsylla burckhardti, teneral adult male. 79. Cacopsylla burckhardti, adult female. 80. Cacopsylla burckhardti, fifth instar immatures. 81. Cacopsylla coccinea, adult male. 82. Cacopsylla coccinea, adult female. 83. Cacopsylla coccinea, fifth instar immatures. 84. Cacopsylla diaphana, adult male. 85 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 78‒85. Habitus. 78. Cacopsylla burckhardti, teneral adult male. 79. Cacopsylla burckhardti, adult female. 80. Cacopsylla burckhardti, fifth instar immatures. 81. Cacopsylla coccinea, adult male. 82. Cacopsylla coccinea, adult female. 83. Cacopsylla coccinea, fifth instar immatures. 84. Cacopsylla diaphana, adult male. 85. Cacopsylla diaphana, adult female. (Photos 79–80 from Cho et al. (2017b), 84–85 from Cho et al. (2017a))

FIGURES 38‒45. Habitus. 38. Homotoma unifasciata, adult female. 39. Homotoma unifasciata, fifth instar immature. 40. Moriphila furva, adult male. 41. Moriphila furva, adult female. 42. Celtisaspis japonica, adult male. 43. Celtisaspis japonica, fifth instar immature. 44 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 38‒45. Habitus. 38. Homotoma unifasciata, adult female. 39. Homotoma unifasciata, fifth instar immature. 40. Moriphila furva, adult male. 41. Moriphila furva, adult female. 42. Celtisaspis japonica, adult male. 43. Celtisaspis japonica, fifth instar immature. 44. Conical gall of Celtisaspis japonica. 45. Lerp of Celtisaspis japonica. (Photos 38–39 from Cho et al. (2017a), 40 from Burckhardt et al. (2018))

FIGURES 126‒133. Habitus. 126. Cacopsylla sangjaei, fifth instar immature. 127. Cacopsylla satsumensis, adult male. 128. Cacopsylla satsumensis, adult female. 129. Cacopsylla satsumensis, immature. 130. Cacopsylla tobirae, adult male. 131. Cacopsylla tobirae, adult female. 132. Cacopsylla tobirae, fifth instar immature. 133 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 126‒133. Habitus. 126. Cacopsylla sangjaei, fifth instar immature. 127. Cacopsylla satsumensis, adult male. 128. Cacopsylla satsumensis, adult female. 129. Cacopsylla satsumensis, immature. 130. Cacopsylla tobirae, adult male. 131. Cacopsylla tobirae, adult female. 132. Cacopsylla tobirae, fifth instar immature. 133. Cacopsylla viburnicola, adult male. (Photos 126–127 from Cho et al. (2017a), 128 from Cho & Lee (2015a))

FIGURES 166‒173. Habitus. 166. Trichochermes grandis, adult male. 167. Trichochermes grandis, adult female. 168. Trichochermes grandis, immature. 169 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula

FIGURES 166‒173. Habitus. 166. Trichochermes grandis, adult male. 167. Trichochermes grandis, adult female. 168. Trichochermes grandis, immature. 169. Marginal gall of Trichochermes grandis. 170. Trioza breviata, adult female. 171. Trioza chilgia, teneral adult male. 172. Trioza chilgia, adult female. 173. Trioza cinnamomi, adult male. (Photos 171–173 from Cho et al. (2017a))