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209 results for “243”
Figure 2 from: Kondratieff BC, DeWalt RE, Verdone CJ (2019) Plecoptera of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 243-254. https://doi.org/10.3897/zookeys.819.23535
Figure 2 Plecoptera species richness by Canadian provinces. Abbreviations: AB – Alberta, BC – British Columbia, MB – Manitoba, NB – New Brunswick, NL – Newfoundland and Labrador, NS – Nova Scotia, NT – Northwest Territories, NU – Nunavut, ON – Ontario, PEI – Prince Edward Island, QC – Quebec, SK – Saskatchewan, and YT – Yukon.
Supplementary material 1 from: Kondratieff BC, DeWalt RE, Verdone CJ (2019) Plecoptera of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 243-254. https://doi.org/10.3897/zookeys.819.23535
: Link: https://doi.org/10.3897/zookeys.819.23535.suppl1
Figures 243-249 from: Lonsdale O (2021) Manual of North American Agromyzidae (Diptera, Schizophora), with revision of the fauna of the "Delmarva" states. ZooKeys 1051: 1-481. https://doi.org/10.3897/zookeys.1051.64603
Figures 243-249 Agromyza vockerothi Spencer, male genitalia 243 external genitalia, posterior 244 external genitalia, anterior 245 external genitalia, left lateral 246 external genitalia, ventral 247 hypandrium and postgonite, ventral 248 phallus, left lateral 249 phallus, ventral.
FIGURE 243 in New species (130) of the hyperdiverse aquatic beetle genus Hydraena Kugelann from Papua New Guinea, and a preliminary analysis of areas of endemism (Coleoptera: Hydraenidae) 2944
FIGURE 243. Hydraena bifunda, holotype, dorsal and lateral habitus, and venter.
FIGURE 243. Picobia heeri Haller, male. A in Quill mites (Acari: Syringophilidae) of the Palaearctic region 2840
FIGURE 243. Picobia heeri Haller, male. A, dorsal view; B, ventral view.
FIGURES 243–253 in The Goblin Spider Genus Costarina (Araneae, Oonopidae), Part 2: the Costa Rican fauna
FIGURES 243–253. Costarina ramon, new species, male (243–248) and female (249–253). 243. Left palp, prolateral view. 244. Same, ventral view. 245. Same, retrolateral view. 246. Left embolus, prolateral view. 247. Same, ventral view. 248. Same, retrolateral view. 249. Sternum, ventral view. 250. Abdomen, lateral view. 251. Same, ventral view. 252. Digested female genitalia, ventral view. 253. Same, dorsal view.
FIGS. 243–257 in The Goblin Spider Genus Costarina (Araneae, Oonopidae), Part 1
FIGS. 243–257. Costarina morales, new species, male (243–251) and female (252–257). 243. Carapace, dorsal view. 244, 252. Same, anterior view. 245. Same, lateral view. 246. Sternum, ventral view. 247. Left embolus, prolateral view. 248. Same, ventral view. 249. Left palp, prolateral view. 250. Same, ventral view. 251. Same, retrolateral view. 253. Abdomen, lateral view. 254. Same, ventral view. 255, 256. Genitalia, ventral view. 257. Same, dorsal view.
Evolution of habitat preference in 243 species of Bent-toed geckos (Genus Cyrtodactylus Gray, 1827) with a discussion of karst habitat conservation
Ancestral state reconstructions of nine different habitat preferences across a phylogeny composed of 76% of the gekkonid genus <i>Cyrtodactylus</i> recover a general habitat preference as being ancestral to all other habitat preferences. The data show that <i>Cyrtodactylus</i> composes an ecologically labile group of species and the frequency of transitioning from a general habitat preference to anything more specialized occurs nearly four times more often than the reverse. Species showing extreme morphological and/or ecological specializations appear to be evolutionary dead ends that do not give rise to species bearing other habitat preferences. Habitat preferences have not evolved randomly across the genus but are generally restricted to clades that tend to occur in specific geographic regions. The largest radiations in the genus occur in rocky habitats (granite and karst), indicating that the transition from a general habitat preference to a granite or karst-dwelling life style is ecologically uncomplicated. Two large, unrelated clades of karst-associated species are centered in northern Indochina and the largest clade of granite-associated species occurs on the Thai-Malay Peninsula. Smaller, independent radiations of clades bearing other habitat preferences occur throughout the tree across the broad distribution of the genus from South Asia to the Western Pacific. With the exception of a general habitat preference, the data show that karst-associated species outnumber all others (28% versus 0.4–10%, respectively) and the common reference to karstic regions as "imperiled arcs of biodiversity" is not only misleading but potentially dangerous. Karstic regions are not simply refugia harboring the remnants of local biodiversity but are foci of speciation that continue to generate the most speciose, independent, radiations across the genus. Unfortunately, karstic landscapes are some of the most imperiled and least protected habitats on the planet and these data continue to underscore the urgent need for their conservation.
Figure 243 from: Houghton D (2012) Biological diversity of the Minnesota caddisflies (Insecta, Trichoptera). ZooKeys 189: 1-389. https://doi.org/10.3897/zookeys.189.2043
Figure 243 - Agrypnia vestita A total specimens collected and all known collecting localities (Figure 4) B monthly adult abundance (1980s to present) C habitat preference (1980s to present) (Table 1) D male genital capsule E phallus.
Figures 243-247 from: Hansson C, Shevtsova E (2012) Revision of the European species of Omphale Haliday (Hymenoptera, Chalcidoidea, Eulophidae). ZooKeys 232: 1-157. https://doi.org/10.3897/zookeys.232.3625
Figures 243-247 - Omphale sti, female: 243 habitus in lateral view, length of specimen 1.5 mm 244 head in frontal view 245 thoracic dorsum 246 transparent wings 247 wing interference patterns.
Figures 243-248 from: Bond J (2012) Phylogenetic treatment and taxonomic revision of the trapdoor spider genus Aptostichus Simon (Araneae, Mygalomorphae, Euctenizidae). ZooKeys 252: 1-209. https://doi.org/10.3897/zookeys.252.3588
Figures 243-248 - Aptostichus derhamgiulianii sp. n.; scale bars = 1.0mm. 243–246 male holotype (AP 415) Inyo County 243 habitus [806016] 244 retrolateral aspect, leg I [806010] 245 prolateral aspect, leg I [806014] 246 retrolateral aspect, pedipalp [806018] 247 male paratype (AP424) from Mono County, retrolateral aspect, leg I [806020] 248 line drawings, spination pattern, leg I tibia and metatarsus of holotype and paratype; retrolateral view, holotype pedipalp.
Figure 3 from: Moon S (2012) Redescription of two Pennellids (Copepoda, Siphonostomatoida) from Korea with a key to species of Peniculus von Nordmann, 1832. ZooKeys 243: 1-14. https://doi.org/10.3897/zookeys.243.3668
Figure 3 - Peniculus minuticaudae Shiino, 1956. Postmetamorphic adult female. A Mandible, ventral B Maxillule, ventral C Maxilla, dorsal D Leg 1, ventral E Leg 2, ventral F Leg 3, ventral G Leg 4, ventral H–J variations of posterior end of trunk with abdomen, dorsal. Scale bars: A–C=25 μm; D–G=50 μm; H–J=200 μm.
Figure 2 from: Moon S (2012) Redescription of two Pennellids (Copepoda, Siphonostomatoida) from Korea with a key to species of Peniculus von Nordmann, 1832. ZooKeys 243: 1-14. https://doi.org/10.3897/zookeys.243.3668
Figure 2 - Peniculus minuticaudae Shiino, 1956. Postmetamorphic adult female. A Habitus, dorsal B Cephalothorax and free thoracic somites, dorsal C Cephalothorax and free thoracic somites, lateral D Posterior end of trunk with abdomen, dorsal E Posterior end of trunk with abdomen, ventral F Egg sac G Caudal ramus H Antenna, dorsal. Scale bars: A=500 μm; B–F=200 μm; G=25 μm; H=50 μm.
Figure 1 from: Moon S (2012) Redescription of two Pennellids (Copepoda, Siphonostomatoida) from Korea with a key to species of Peniculus von Nordmann, 1832. ZooKeys 243: 1-14. https://doi.org/10.3897/zookeys.243.3668
Figure 1 - Map showing the marine ranched fish farming facility, Tongyeong marine living resources research & conservation center (TMRC), Tongyeong, Gyeongsangnam-do, Korea
Figure 5 from: Moon S (2012) Redescription of two Pennellids (Copepoda, Siphonostomatoida) from Korea with a key to species of Peniculus von Nordmann, 1832. ZooKeys 243: 1-14. https://doi.org/10.3897/zookeys.243.3668
Figure 5 - Peniculus truncatus Shiino, 1956. Postmetamorphic adult female. A Maxillule, dorsal B Maxilla, dorsal C Leg 1, ventral D Leg 2, ventral E Leg 3, ventral F Leg 4, ventral. Scale bars: A, B=25 μm; C–F=50 μm.
Figure 4 from: Moon S (2012) Redescription of two Pennellids (Copepoda, Siphonostomatoida) from Korea with a key to species of Peniculus von Nordmann, 1832. ZooKeys 243: 1-14. https://doi.org/10.3897/zookeys.243.3668
Figure 4 - Peniculus truncatus Shiino, 1956. Postmetamorphic adult female. A. Habitus, dorsal B Cephalothorax and free thoracic somites, lateral C Cephalothorax and free thoracic somites, dorsal D Posterior end of trunk with abdomen, ventral E Caudal ramus, ventral F Antenna, dorsal G Mandible, ventral. Scale bars: A=500, μm; B–D=200 μm; E, G=25 μm; F=50 μm.
Figure 4 from: Jozwiak P, Jakiel A (2012) A new genus and new species of Agathotanaidae (Crustacea, Tanaidacea) from West Australia. ZooKeys 243: 15-26. https://doi.org/10.3897/zookeys.243.3408
Figure 4 - Bunburia prima sp. n., allotype male. A body, dorsal view B antennule C cheliped D pleopod. Scale line = 0.1 mm.
Figure 3 from: Jozwiak P, Jakiel A (2012) A new genus and new species of Agathotanaidae (Crustacea, Tanaidacea) from West Australia. ZooKeys 243: 15-26. https://doi.org/10.3897/zookeys.243.3408
Figure 3 - Bunburia prima sp. n., paratype female. A pereopod 1 A' detailes of P1 propodus B pereopod 2 C pereopod 3 D pereopod 4 E pereopod 5 F pereopod 6 F' details of P6 propodus G uropod. Scale line = 0.1 mm.
Figure 2 from: Jozwiak P, Jakiel A (2012) A new genus and new species of Agathotanaidae (Crustacea, Tanaidacea) from West Australia. ZooKeys 243: 15-26. https://doi.org/10.3897/zookeys.243.3408
Figure 2 - Bunburia prima sp. n., paratype female. A labrum B mandible molar B' incisor of right mandible C left mandible D maxillule endite D details of distal part of maxillule E maxilla F labium G maxilliped H epignath. Scale line = 0.1 mm.
Figure 1 from: Jozwiak P, Jakiel A (2012) A new genus and new species of Agathotanaidae (Crustacea, Tanaidacea) from West Australia. ZooKeys 243: 15-26. https://doi.org/10.3897/zookeys.243.3408
Figure 1 - Bunburia prima sp. n., holotype female. A body, dorsal view; paratype female B antennule C antenna (proximal article not shown) D cephalothorax, ventral view E cheliped E' details of fixed finger and dactylus F pleotelson, ventral view. Scale lines = 1 mm for A and 0.1 mm for B–E.
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