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FIGURES 5–10. 5, 7, 8, 9, 10. Oncopeltus orourkeae, holotype male. 5 in A new species of Oncopeltus Stål, 1868 (Heteroptera: Lygaeidae) in the nominate subgenus from Ecuador
FIGURES 5–10. 5, 7, 8, 9, 10. Oncopeltus orourkeae, holotype male. 5. Head and pronotum, dorsal view (Total body length=15.6 mm), 7. Clasper, latero-external view (lateral process side), 8. Clasper, latero-ventral view, 9. Clasper, latero-internal view, 10. Pygophore, ventral view. 6. Oncopeltus varicolor, male, head and pronotum, dorsal view (Total body length=16.2 mm).
FIGURES 1–4. 1, 3, 4. Oncopeltus orourkeae, holotype male. 1 in A new species of Oncopeltus Stål, 1868 (Heteroptera: Lygaeidae) in the nominate subgenus from Ecuador
FIGURES 1–4. 1, 3, 4. Oncopeltus orourkeae, holotype male. 1. Habitus (Total body length= 15.6 mm), 3. Lateral view of head and thorax. 4. Detail of margin of hemelytra and pilosity.. 2. Oncopeltus varicolor, male, habitus (Total body length=16.2 mm).
and metatarsal trichobothria as well as the bristles and the tibial and metatarsal bristleshaped hairs are drawn but no normal hairs; 6) retrolateral aspect of the left retroclaw IV; 7) genital area in front of the epigastral furrow in which no epiandrous gland spigots are recognizable. Not all of the hairs anteriorly of the pit are drawn; 8) outline of the anterior spinnerets, ventral aspect; 9) retrolateral aspect of the right pedipalpus; 10) prolateral aspect of the right pedipalpus. Only two of the long retrolateral bristle-shaped cymbial hairs are drawn; 11) ventral aspect of the right pedipalpus; 12) slightly different retroventral aspects of the distal part of the right pedipalpus. C = conductor, E = embolus, M = median apophysis, O = proventral-distal outgrowth of the pedipalpal tibia. Scale bars 0.5 mm in figs. 1-2 and 5, 0.05 in fig. 4 and 6, 0.1 in fig. 7, 0.2 in the remaining figs; in On European Spiders Of The Nominal Families Liocranidae, Miturgidae And Zoridae (Araneae), With Descriptions Of New Taxa
and metatarsal trichobothria as well as the bristles and the tibial and metatarsal bristleshaped hairs are drawn but no normal hairs; 6) retrolateral aspect of the left retroclaw IV; 7) genital area in front of the epigastral furrow in which no epiandrous gland spigots are recognizable. Not all of the hairs anteriorly of the pit are drawn; 8) outline of the anterior spinnerets, ventral aspect; 9) retrolateral aspect of the right pedipalpus; 10) prolateral aspect of the right pedipalpus. Only two of the long retrolateral bristle-shaped cymbial hairs are drawn; 11) ventral aspect of the right pedipalpus; 12) slightly different retroventral aspects of the distal part of the right pedipalpus. C = conductor, E = embolus, M = median apophysis, O = proventral-distal outgrowth of the pedipalpal tibia. Scale bars 0.5 mm in figs. 1-2 and 5, 0.05 in fig. 4 and 6, 0.1 in fig. 7, 0.2 in the remaining figs;
Figs. 1-12 in On European Spiders Of The Nominal Families Liocranidae, Miturgidae And Zoridae (Araneae), With Descriptions Of New Taxa
Figs. 1-12: Mesiotelus qrancanariensis WUNDERLICH 1992, ♂ from Portugal; 1) Dorsal aspect of the prosoma. Only small fields of the long cheliceral and the dense prosomal hairs are drawn; 2) ventral aspect of the mouth parts. Only few hairs are drawn; 3) retroventral aspect of the left fang which is strongly bent in the basal half; 4) feathery (branched) hair of the left coxa I; 5) prolateral aspect of the right leg I. The tarsal
figs. 17a-d in On European Spiders Of The Nominal Families Liocranidae, Miturgidae And Zoridae (Araneae), With Descriptions Of New Taxa
figs. 17a-d: Apostenus qrancanariensis WUNDERLICH 1992, ♂; 17a) tiny bristles of the ventral-medial part of the opisthosoma; 17b) ventral aspect of the left bulbus; the arrow points to the opening of the sperm duct; 17c) dorsal aspect of the right pedipalpal tibia; 17d) dorsal aspect of the left pedipalpal tibia: A malformation with an additional apophysis (arrow). Scale bar 0.1;
FIGURE 6 in Re-evaluation of the taxonomic status of four nominal, western Pacific species of tongue soles (Pleuronectoidei: Cynoglossidae: Cynoglossus), with redescription of C. joyneri Günther, 1878
FIGURE 6. Maximum-likelihood (ML) phylogeny of selected species of Cynoglossus from the northwestern Pacific Ocean based on 12S rRNA and COI gene fragments. Taxon listed as "NCBI" indicates 12S (LC049621) and COI (KF979127) gene fragments downloaded from GenBank. Numbers above nodes indicate bootstrap values in percentage (based on 100 replicates). Values below 70% not shown.
FIGURE 5 in Re-evaluation of the taxonomic status of four nominal, western Pacific species of tongue soles (Pleuronectoidei: Cynoglossidae: Cynoglossus), with redescription of C. joyneri Günther, 1878
FIGURE 5. Photographs of specimens representing the three groups of tongue soles identified in this study. A) First group featuring wider body and shorter rostral hook. B) Second group featuring narrower body and longer rostral hook. C) Third group: C-1) featuring wider body and longer rostral hook; C-2) featuring narrower body and shorter rostral hook. Photos: A and C-1 by H.-R. Luo; B and C-2 by X.-Y. Kong.
FIGURE 3 in Re-evaluation of the taxonomic status of four nominal, western Pacific species of tongue soles (Pleuronectoidei: Cynoglossidae: Cynoglossus), with redescription of C. joyneri Günther, 1878
FIGURE 3. Hand-drawn sketches illustrating different positions of posterior tip of rostral hook relative to anterior margin of lower eye (PHE). A) Tip not reaching anterior margin of eye (PHE> 0); B) Tip reaching vertical at anterior margin of eye (PHE = 0); C) Tip reaching vertical slightly beyond anterior margin of eye (PHE <0).
FIGURE 2. Twenty-two sampling locations for 138 in Re-evaluation of the taxonomic status of four nominal, western Pacific species of tongue soles (Pleuronectoidei: Cynoglossidae: Cynoglossus), with redescription of C. joyneri Günther, 1878
FIGURE 2. Twenty-two sampling locations for 138 specimens of tongue soles examined in this study.Abbreviations for locations are: NJ: Niphon; SJ: Shizuoka; KJ: Kochi; QH: Qinhuangdao; YT: Yantai; QD: Qingdao; RZ: Rizhao; LY: Lianyungang; LS: Lvsi; SH: Shanghai; ZS: Zhoushan; WL: Wenling; WZ: Wenzhou; FZ: Fuzhou; MW: Mawei; XM: Xiamen; DS: Dongshandao; SW: Shanwei; SZ: Shenzhen; ZH: Zhuhai; JM: Jiangmen; BM: Baimajing.
FIGURE 1 in Re-evaluation of the taxonomic status of four nominal, western Pacific species of tongue soles (Pleuronectoidei: Cynoglossidae: Cynoglossus), with redescription of C. joyneri Günther, 1878
FIGURE 1. Photographs of ocular sides of lectotypes of two nominal species of Cynoglossus. A) Cynoglossus joyneri (BMNH 1878.4.15.94, 232.6 mm SL); and B) Cynoglossus lighti (BMNH 1924.12.15.87, 172.0 mm SL). Photos by K. Webb (Natural History Museum, London).
FIGURE 4 in Re-evaluation of the taxonomic status of four nominal, western Pacific species of tongue soles (Pleuronectoidei: Cynoglossidae: Cynoglossus), with redescription of C. joyneri Günther, 1878
FIGURE 4. Close-up photographs of heads of lectotypes of: A) Cynoglossus joyneri; and B) Cynoglossus lighti. Preorbital lateral lines indicated by arrows. Photos by J. Maclaine and K. Webb (Natural History Museum, London).
FIGURE 3 in A taxonomic study on the nominate subgenus Macrolycus Waterhouse, 1878 from China (Coleoptera, Lycidae)
FIGURE 3. Aedeagi of Macrolycus species, dorsal views: A–C. M. oreophilus Kazantsev, 2002; D–F. M. gansuensis Kazantsev, 2002; G–I. M. bowringi Waterhouse, 1878; J–L. M. subapicis sp. nov. (holotype). A, D, G, J: dorsal views; B, E, H, K: ventral views; C, F, I, L: lateral views. Scale bars: 1.0 mm.
FIGURE 2 in A taxonomic study on the nominate subgenus Macrolycus Waterhouse, 1878 from China (Coleoptera, Lycidae)
FIGURE 2. Male habitus of Macrolycus species, dorsal views: A. M. oreophilus Kazantsev, 2002; B. M. gansuensis Kazantsev, 2002; C. M. bowringi Waterhouse, 1878; D. M. subapicis sp. nov. (holotype). Scale bars: 1.0 mm.
Database of the Western South Slavic Verb HyperVerb (WeSoSlaV) – Deverbal Nominalizations
<p>This dataset includes the annotation of deverbal nominalizations in two South Slavic languages, Bosnian/Croatian/Serbian/Montenegrin (BCMS) and Slovenian, as part of the Database of the Western South Slavic Verb (WeSoSlaV), which focuses on the most frequent verbs in these two languages (see WeSoSlaV_nominalizations_instructions).</p> <p> </p>
Subspecies and Distribution. A. p. palliata Gray, 1849 — NE Guatemala (Rio Motagua, and possibly along the coast a short distance to Cabo de Tres Puntas, where it meets the distribution of the Central American Black Howler, A. pigra), E to E Costa Rica or W Panama; it is not found in El Salvador, although it may have occurred there in the past. A. p. aequatorialis Festa, 1903 — from the S distributional limits of the nominate subspecies palliata (either in E Costa Rica or W Panama) through the Serrania del Darién into W Colombia (N through basins of the rios Sint and Atrato to the Caribbean coast, and S through the Serrania del Baudo and the foothills, lowlands, and lower montane areas W of the Andes to the Pacific coast), W Ecuador, and NW Peru (extreme N of Tumbes Department). A. p. coibensis Thomas, 1902 — SW Panama (Coiba and Jicaron Is). A. p. mexicana Merriam, 1902 — S & SE Mexico (states of Veracruz, Tabasco, Campeche, Oaxaca, and N Chiapas) and Guatemala, in a swathe skirting the S of the distribution of the Central American Black Howler. A. p. trabeata Lawrence, 1933 — SW Panama (Azuero Peninsula). in Atelidae
Subspecies and Distribution. A. p. palliata Gray, 1849 — NE Guatemala (Rio Motagua, and possibly along the coast a short distance to Cabo de Tres Puntas, where it meets the distribution of the Central American Black Howler, A. pigra), E to E Costa Rica or W Panama; it is not found in El Salvador, although it may have occurred there in the past. A. p. aequatorialis Festa, 1903 — from the S distributional limits of the nominate subspecies palliata (either in E Costa Rica or W Panama) through the Serrania del Darién into W Colombia (N through basins of the rios Sint and Atrato to the Caribbean coast, and S through the Serrania del Baudo and the foothills, lowlands, and lower montane areas W of the Andes to the Pacific coast), W Ecuador, and NW Peru (extreme N of Tumbes Department). A. p. coibensis Thomas, 1902 — SW Panama (Coiba and Jicaron Is). A. p. mexicana Merriam, 1902 — S & SE Mexico (states of Veracruz, Tabasco, Campeche, Oaxaca, and N Chiapas) and Guatemala, in a swathe skirting the S of the distribution of the Central American Black Howler. A. p. trabeata Lawrence, 1933 — SW Panama (Azuero Peninsula).
Nominalization and Its Various Functions in Liangmai
<p>Nominalization is highly productive and widely attested in normal discourse and speech in Liangmai. Both lexical and clausal nominalizations are found in the language. Different nominalizing affixes and its functions are discussed. Nominalized form of verb functions as verbal noun, gerund, infinitive, adjectival and agentive. Nominalization also produces various types of syntactic structures, such as nominalized clause, relative clause and complement clause. The nominalizer -bo is most productive and is plurifunctional.</p>
Nominal Anchoring Functions of Porohanon Common Noun Markers
<p>Porohanon, spoken in the Municipality of Poro, Camotes, Cebu, Philippines is a member of the Peripheral group of the Central Bisayan branch of the Bisayan complex. This study proposes a SPECIFIC vs. NONSPECIFIC contrast in the ABSOLUTIVE, ERGATIVE, and GENITIVE forms of the common noun markers, instead of a DEFINITE vs. INDEFINITE contrast stated in previous descriptions of the speech variety.</p>
Data for the article on 'Nominal and pronominal negative concord, through the lens of Belizean and Jamaican Creole' by J. van der Auwera, published in Linguistics
<p>Data for the article on 'Nominal and pronominal negative concord, through the lens of Belizean and Jamaican Creole' by J. van der Auwera, published in Linguistics</p>
Subspecies and Distribution. M.h.hasselti:Temminck,1840—MalayPeninsula(includingoffshoreLangkawiI),RiauArchipelago,SWSumatra(BukitBarisanSelatanNationalPark),Java,andSumbawaI. M.h.abbottiLyon,1916—MentawaiIs,offWSumatra. M.h.continentisShamel,1942—patchilydistributedinSEAsia. M. h. macellus Temminck, 1840 — Borneo, also E India (West Bengal) and Sri Lanka; but S Asian populations are assigned to the nominate subspecies by some authors. One record from S China (Yunnan), subspecies not known. in Vespertilionidae
Subspecies and Distribution. M.h.hasselti:Temminck,1840—MalayPeninsula(includingoffshoreLangkawiI),RiauArchipelago,SWSumatra(BukitBarisanSelatanNationalPark),Java,andSumbawaI. M.h.abbottiLyon,1916—MentawaiIs,offWSumatra. M.h.continentisShamel,1942—patchilydistributedinSEAsia. M. h. macellus Temminck, 1840 — Borneo, also E India (West Bengal) and Sri Lanka; but S Asian populations are assigned to the nominate subspecies by some authors. One record from S China (Yunnan), subspecies not known.
Subspecies and Distribution. C. p. paca Linnaeus, 1766 — E & S Colombia, Venezuela, the Guianas, and E Brazil to Paraguay, N Argentina (Misiones and Corrientes provinces), and Uruguay. C. p. guanta Lonnberg, 1921 — W Brazil, Ecuador, Peru, and N Bolivia. C. p. mexianae Hagmann, 1908 — E Brazil, mouth of the Amazon in Para State. C. p. nelsoni Goldman, 1913 — E & S Mexico (Atlantic slope lowlands from San Luis Potosi State to Yucatan Peninsula), then through Central America to N Costa Rica. C. p. virgatus Bangs, 1902 — W Costa Rica, through Panama to N & W Colombia. It is also naturally present in Trinidad and Tobago Is (subspecies unknown), but it was extinct in Tobago I long ago due to overexploitation by Amerindians. They also introduced the Lowland Paca (nominate subspecies) from Venezuela into Curacao I, the largest of the Netherlands Antilles. In the 20" century it was successfully introduced into Cuba from Mexico, so it should belong to the Mexican subspecies nelson in Cuniculidae
Subspecies and Distribution. C. p. paca Linnaeus, 1766 — E & S Colombia, Venezuela, the Guianas, and E Brazil to Paraguay, N Argentina (Misiones and Corrientes provinces), and Uruguay. C. p. guanta Lonnberg, 1921 — W Brazil, Ecuador, Peru, and N Bolivia. C. p. mexianae Hagmann, 1908 — E Brazil, mouth of the Amazon in Para State. C. p. nelsoni Goldman, 1913 — E & S Mexico (Atlantic slope lowlands from San Luis Potosi State to Yucatan Peninsula), then through Central America to N Costa Rica. C. p. virgatus Bangs, 1902 — W Costa Rica, through Panama to N & W Colombia. It is also naturally present in Trinidad and Tobago Is (subspecies unknown), but it was extinct in Tobago I long ago due to overexploitation by Amerindians. They also introduced the Lowland Paca (nominate subspecies) from Venezuela into Curacao I, the largest of the Netherlands Antilles. In the 20" century it was successfully introduced into Cuba from Mexico, so it should belong to the Mexican subspecies nelson
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