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40 results for “woodlice”
Supplementary material 2 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Rhinophoridae larva from a Neotropical woodlouse species :
Figure 5 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 5 Rhinophoridae larva obtained from the Neotropical isopod Balloniscusglaber. Morphotype 2, 3rd instar A dorsal view B detail from anterior part showing the cephaloskeleton and anterior spiracles C detail of the posterior spiracle.
Figure 4 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 4 Rhinophoridae larva obtained from the Neotropical isopod Balloniscusglaber. Morphotype 1, 3rd instar A detail view of the cephaloskeleton on dorsal view B detail view of the anterior spiracle C alive larva with transparent integument D fixed larva, dorsal view.
Figure 3 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 3 Balloniscusglaber infected with 3rd instar Rhinophoridae larva A alive B.glaber clinging to the substrate B secretion discharged from uropod glands C–D dorsal (C) and ventral (D) views of Balloniscusglaber with a third instar Rhinophoridae larva inside E–F partially dissected Balloniscusglaber infected with Rhinophoridae larva showing the empty gut on dorsal view (E) and the calcium plates on ventral view (F).
Figure 2 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 2 Distribution map of native and introduced Rhinophoridae species in the Neotropical region (area in gray) including the new larvae record. Apomorphytoinbio records from Pape (2010) and Cerretti et al. (2014); Bezzimyia spp. records from Pape and Arnaud (2001); Shannoniella spp. records from Nihei et al. (2016); Trypetidomima spp. records from Nihei and Andrade (2014); Melanophoraroralis records from Parker (1953), Guimarães (1977), González (1998), Cerretti and Pape (2009) and Mulieri et al. (2010); Steveniadeceptoria records from Mulieri et al. (2010). Base map modified from: commons.wikimedia.org/
Figure 1 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 1 Schematic representation of the infection cycle of a Rhinophoridae fly in a woodlouse host. 3 is modified from Thompson (1934).
Figure 8 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 8 Scanning electron (A, C, E, G) and light microscope (B, D, F, H) micrographs on the studied Armadillidium species' tergites. Armadillidiumvulgare (A, B), A.versicolor (C, D), A.nasatum (E, F), A.zenckeri (G, H). Abbreviations: pl – plaques, t – tricorn receptor. Staining: hematoxylin-eosin (HE) – B, D, F, H. Scale bars: 50 µm.
Figure 5 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 5 Intrageneric (between the two specimens per species) comparison of tergal cuticle thickness in four Armadillidium species (2 specimens/species, 5 slides/specimen, 10 measurements/slide). [Measures: median ± first quartile and max/min (Species names as in Figure 3)].
Figure 6 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 6 Light microscope micrographs of the studied species' tergites. Armadillidiumvulgare (A), Cylisticusconvexus (B), Orthometoponplanum (C), Protracheoniscuspolitus (D), Porcellionidespruinosus (E), Trachelipusrathkii (F). Abbreviations: ec – epicuticle, pc – procuticle, p – polysaccharide spheres, t – tricorn receptor, n – nerve; x 63. Staining: hematoxylin-eosin (HE) – A, E, F; Periodic Acid-Schiff (PAS) – B, C, D. Scale bars: 50 µm.
Figure 2 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 2 Mass-specific water loss at ~30% relative humidity. s – surviving individuals, d – dead individuals. [Measures: median ± first quartile and max/min (species names as in Figure 1)].
Figure 7 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 7 The dorsal surface of the studied sympatric terrestrial isopod species. Armadillidiumvulgare (A), Cylisticusconvexus (B), Orthometoponplanum (C), Protracheoniscuspolitus (D), Porcellionidespruinosus (E), Trachelipusrathkii (F). Abbreviations: pl – plaques, p – polysaccharide spheres, t – tricorn receptor. Scale bars: 50 µm.
Figure 5 from: De Smedt P, Boerave P, Arijs G, Segers S (2018) Woodlice of Belgium: an annotated checklist and bibliography (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 265-304. https://doi.org/10.3897/zookeys.801.21894
Figure 5 Six of the nine species added to this new checklist, aPorcelliomonticolabElumacaelatacHyloniscusripariusdTrichoniscoidessarsiePhilosciaaffinis and fMetatrichoniscoidesleydigii; photos: Gert Arijs.
Figure 3 from: De Smedt P, Boerave P, Arijs G, Segers S (2018) Woodlice of Belgium: an annotated checklist and bibliography (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 265-304. https://doi.org/10.3897/zookeys.801.21894
Figure 3 Map of Belgium with the UTM 10×10 km grid. The different colours indicate the different topographical regions used to determine the species status.
Figure 1 from: De Smedt P, Boerave P, Arijs G, Segers S (2018) Woodlice of Belgium: an annotated checklist and bibliography (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 265-304. https://doi.org/10.3897/zookeys.801.21894
Figure 1 Cumulative number of species published as part of the native fauna of Belgium between 1831 (five species) and 2017 (36 species). Exotic species exclusively living in greenhouses were omitted.
Figure 4 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 4 The tergal cuticle thickness in intra-, and interspecific relations (2 specimens/species, 5 slides/specimen, 10 measurements/slide). [Measures: median ± first quartile and max/min (species names as in Figure 1)].
Figure 3 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 3 Mass-specific water loss of the survived individuals at the three different relative humidity values (white: ~30%, medium gray: ~75%, dark grey: ~100%). The experiment took 6 hours. [Measures: median ± first quartile and max/min; in species names A. means Armadillidium]
Figure 1 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 1 Mass-specific water loss of the survived individuals (*all individuals died) at three different relative humidity values (white: ~30%, medium gray: ~75%, dark grey: ~100%). The experiment took 6 hours. [Measures: median ± first quartile and max/min; species initials: P.politus – Protracheoniscuspolitus, O.planum – Orthometoponplanum, C.convexus – Cylisticusconvexus, T.rathkii – Trachelipusrathkii, P.pruinosus – Porcellionidespruinosus, A.vulgare – Armadillidiumvulgare].
Figure 1 from: Devigne C, Broly P, Mullier R, Deneubourg J (2012) Aggregation in woodlice: social interaction and density effects. ZooKeys 176: 133-144. https://doi.org/10.3897/zookeys.176.2258
Figure 1 - Experimental set-up.
Figure 4 from: De Smedt P, Boerave P, Arijs G, Segers S (2018) Woodlice of Belgium: an annotated checklist and bibliography (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 265-304. https://doi.org/10.3897/zookeys.801.21894
Figure 4 Map of Belgium with the number of species per square of the UTM 10×10 km grid.
Figure 2 from: De Smedt P, Boerave P, Arijs G, Segers S (2018) Woodlice of Belgium: an annotated checklist and bibliography (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 265-304. https://doi.org/10.3897/zookeys.801.21894
Figure 2 Cumulative number of publications on Belgian woodlice from 1831 until 2017.
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