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1,669 results for “Isopod”
Figure 1 from: Derbák D, Dányi L, Hornung E (2018) Life history characteristics of a cave isopod (Mesoniscus graniger Friv.). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 359-370. https://doi.org/10.3897/zookeys.801.23391
Figure 1 a Sexual dimorphism of Mesoniscusgraniger. Scale bar 500 µm. Key: 1st Pl-ex – first pleopodite-exopodite, Pl-en – pleopodite-endopodite b black line – head-width measurement.
Figure 7 from: Nako J-D, Lee NS, Wright JC (2018) Water vapor absorption allows for volume expansion during molting in Armadillidium vulgare and Porcellio dilatatus (Crustacea, Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 459-479. https://doi.org/10.3897/zookeys.801.23344
Figure 7 A Percentage mass change between 5 days premolt and anterior ecdysis for Armadillidiumvulgare maintained in 100 % RH (blue) and 97 % RH (red) and plotted as a function of premolt mass. Trendlines show best-fit logarithmic curves. Animals in 97 % RH achieve slightly smaller proportional mass changes to those in saturated air, consistent with the reduced vapor pressure gradient for WVAB Log-log plot showing the relationship between fractional mass-gain and pre-molt mass in 100 % RH (% mass gain α M-0.676).
Figure 3 from: Nako J-D, Lee NS, Wright JC (2018) Water vapor absorption allows for volume expansion during molting in Armadillidium vulgare and Porcellio dilatatus (Crustacea, Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 459-479. https://doi.org/10.3897/zookeys.801.23344
Figure 3 Mass changes of Porcelliodilatatus during molting at 100 % RH, without access to food. Bars show ± SEM with sample sizes.
Figure 5 from: Kashani GM, Abedini A, Montesanto G (2018) Terrestrial isopods of the family Eubelidae Budde-Lund, 1899 from Iran, with description of a new species (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 177-187. https://doi.org/10.3897/zookeys.801.23340
Figure 5 Koweitoniscusshafieii sp. n., male, paratype. A pereopod 1 B pereopod 7 C pleopod 1 endopodite with enlarged apex D pleopod 1 exopodite E pleopod 2 F pleopod 3 exopodite G pleopod 4 exopodite H pleopod 5 exopodite.
Figure 2 from: Antoł A, Czarnoleski M (2018) Size dependence of offspring production in isopods: a synthesis. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 337-357. https://doi.org/10.3897/zookeys.801.23677
Figure 2 In Porcellioscaber, the heaviest offspring were released by large females that produced small clutches. The plane represents a multiple regression model fitted to the data; the partial slopes depicted on the edges were calculated by setting the other predictor value to its minimum and maximum values.
Figure 8 from: Sfenthourakis S, Hornung E (2018) Isopod distribution and climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 25-61. https://doi.org/10.3897/zookeys.801.23533
Figure 8 The expansion of Armadillidiumvulgare in North-America (modified after Garthwaite et al. 1995).
Figure 11 from: Gongalsky KB, Turbanov IS, Medvedev DA, Volkova JS (2018) Description of a new species of the genus Protracheoniscus Verhoeff, 1917 and redescription of Protracheoniscus kryszanovskii Borutzky, 1957 from the southeast of European Russia (Isopoda, Oniscidea, Agnaridae). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 189-205. https://doi.org/10.3897/zookeys.801.23167
Figure 11 Phylogeny of six species of the genera Protracheoniscus and Desertoniscus with outgroup taxa based on the analysis of the mtDNA COI gene by the Neighbor Joining method (NJ) with the calculation of bootstrap support of branch sites (1000 replications).
Figure 1 from: Gongalsky KB, Turbanov IS, Medvedev DA, Volkova JS (2018) Description of a new species of the genus Protracheoniscus Verhoeff, 1917 and redescription of Protracheoniscus kryszanovskii Borutzky, 1957 from the southeast of European Russia (Isopoda, Oniscidea, Agnaridae). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 189-205. https://doi.org/10.3897/zookeys.801.23167
Figure 1 Dorsal view of male paratype of Protracheoniscuspokarzhevskii sp. n., 4 mm (A), and male ProtracheoniscuskryszanovskiiBorutzky 1957, 9 mm (B), from Kalmykia, SE of European Russia.
Figure 10 from: Gongalsky KB, Turbanov IS, Medvedev DA, Volkova JS (2018) Description of a new species of the genus Protracheoniscus Verhoeff, 1917 and redescription of Protracheoniscus kryszanovskii Borutzky, 1957 from the southeast of European Russia (Isopoda, Oniscidea, Agnaridae). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 189-205. https://doi.org/10.3897/zookeys.801.23167
Figure 10 Distribution in the SE of European Russia of Protracheoniscuskryszanovskii from the original description by Borutzky (1957) (circles) and new location on Sarpa Lake, Kalmykia (square), and location of Protracheoniscuspokarzhevskii sp. n. in Bolshoi Tsaryn (diamond).
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 2 from: Montesanto G (2018) Presence of a stridulatory apparatus in the manca stages of isopods (Crustacea, Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 501-518. https://doi.org/10.3897/zookeys.801.23018
Figure 2 Armadilloofficinalis Duméril, 1816. A manca stage M I, antennal flagellum B manca stage M II, antennal flagellum C manca stage M II, aesthetascs on the second article of antennal flagellum D manca stage M III, antennal flagellum E manca stage M II, eye F manca stage M III, eye G manca stage M I, p7: pereonite 7 H manca stage M II, p7: pereonite 7 I manca stage M III, p7: pereonite 7, e: epimeron. Scale bars: 10 μm (C, E); 50 μm (A, B, D, F); 100 μm (G, H); 500 μm (I).
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 3 from: Hornung E, Kásler A, Tóth Z (2018) The role of urban forest patches in maintaining isopod diversity (Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 371-388. https://doi.org/10.3897/zookeys.801.22829
Figure 3 Box plots of urbanisation intensity (UI) according to vegetation characteristics. Horizontal line within a box indicates the median.
Figure 1 from: Montesanto G (2018) Presence of a stridulatory apparatus in the manca stages of isopods (Crustacea, Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 501-518. https://doi.org/10.3897/zookeys.801.23018
Figure 1 Correlation between cephalothorax widths of the ovigerous females with the number of mancas released.
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 2 from: Hornung E, Kásler A, Tóth Z (2018) The role of urban forest patches in maintaining isopod diversity (Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 371-388. https://doi.org/10.3897/zookeys.801.22829
Figure 2 PCA biplot of the sample sites according to the urbanisation variables. Abbreviations: B - mean building density, B2 - number of cells with high building density, S: number of cells with road, V: mean vegetation density, V2: number of cells with high vegetation density. Numbers are sample site (same as in Fig. 1). Symbols indicate rural (▲) and disturbed (●) habitats.
Figure 8 from: Bogataj U, Praznik M, Mrak P, Štrus J, Tušek-Žnidarič M, Žnidaršič N (2018) Comparative ultrastructure of cells and cuticle in the anterior chamber and papillate region of Porcellio scaber (Crustacea, Isopoda) hindgut. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 427-458. https://doi.org/10.3897/zookeys.801.22395
Figure 8 Ultrastructure of the apical plasma membrane labyrinth in the anterior chamber and the papillate region. A Apical membrane labyrinth (AL) in the anterior chamber. In the cytoplasmic strands mitochondria (arrowheads) are present B A tubular appearance of cytoplasmic strands is evident in certain sections (arrow) C Apical membrane labyrinth (AL) in the papillate region. Key: arrowheads – mitochondria, CUT – cuticle.
Figure 6 from: Montesanto G (2018) Presence of a stridulatory apparatus in the manca stages of isopods (Crustacea, Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 501-518. https://doi.org/10.3897/zookeys.801.23018
Figure 6 Armadilloofficinalis Duméril, 1816. Manca stage M II. A pereopod 4 (p4) and pereopod 5 (p5) showing the line of scales on the propodus B epimera of pereonite 4 (e4), pereonite 5 (e5), and pereonite 6 (e6), ventral view C epimera of pereonite 5, ventral view D epimera of pereonite 6, ventral view. Scale bars: 50 μm (A, C, D); 100 μm (B).
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