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114 results for “Zodarion”
Figure 1 in Description of a new Zodarion Walckenaer, 1826 from Turkey (Zodariidae; Araneae)
Figure 1. Zodarion bigaense sp. nov. A) Male palp, ventral view; B) Male palp, retrolateral view; C) Epigyne; D) Vulva – Z. turcicum Wunderlich, 1980; E) Male palp, ventral view; F) Male palp, retrolateral view; G) Epigyne; H) Vulva. Scale bars: 0.5 mm.
Figure 3 in The impact of predation by the myrmecophagous spider Zodarion elegans (Araneae: Zodariidae) on the activity pattern of the Mediterranean harvester ant Messor wasmanni (Hymenoptera: Formicidae)
Figure 3 Foraging activity of ants leaving the nest in correlation with absence/presence of Z. elegans individuals. Activity per day was measured as the number of leaving plus returning worker ants per min in a half-hour intervals; counts were summarized per day (0 = absence of Z. elegans, 1 = presence of Z. elegans).
Figure 5 in The impact of predation by the myrmecophagous spider Zodarion elegans (Araneae: Zodariidae) on the activity pattern of the Mediterranean harvester ant Messor wasmanni (Hymenoptera: Formicidae)
Figure 5. Tasks performed by marked foragers inside the nest when nest entrances were closed due to predation pressure. The number of workers per activity was summarized during the duration of three perturbation experiments. Per experiment 30 workers – 10 Minor-workers, 10 Medium-workers and 10 Major-workers – were marked.
Figure. 4 in The impact of predation by the myrmecophagous spider Zodarion elegans (Araneae: Zodariidae) on the activity pattern of the Mediterranean harvester ant Messor wasmanni (Hymenoptera: Formicidae)
Figure. 4 Foraging activity of ants returning to the nest in correlation with absence/presence of Z. elegans individuals. Scores were taken during half-hour intervals (0 = absence of Z. elegans, 1 = presence of Z. elegans).
Figure 1 in The impact of predation by the myrmecophagous spider Zodarion elegans (Araneae: Zodariidae) on the activity pattern of the Mediterranean harvester ant Messor wasmanni (Hymenoptera: Formicidae)
Figure 1. Frequency of Z. elegans individuals found within a distance of max. 0.5 m to active/inactive ant colonies in a) spring 2009, b) summer 2009 and c) autumn 2009 (1 = active colonies, 0 = inactive colonies).
Figure 2 in The impact of predation by the myrmecophagous spider Zodarion elegans (Araneae: Zodariidae) on the activity pattern of the Mediterranean harvester ant Messor wasmanni (Hymenoptera: Formicidae)
Figure 2 Flow diagram of nest entrance closure in response to prey capture by the spider Z. elegans. In total, four experiments were performed with an overall duration of 100 days (Trial 1: n = 20, Trial 2: n = 30, Trial 3: n = 30, Trial 4: n = 20, n(total) = 100). The capture of M. wasmanni workers by Z. elegans is necessary to prompt ants to end aboveground activity and close nest entrances. By contrast, the presence of spiders in the formicarium alone was not sufficient to prompt ants to close nest entrances after aboveground foraging activity ceased.
Figure 9 in Contributions to the genus Zodarion Walckenaer, 1826 in Turkey, with the description of a new species (Araneae: Zodariidae)
Figure 9. Zodarion kunti sp.n., drawings of male palp, A. Retrolateral view; B. Ventral view (Scale: 0.2).
Figure 8 in Contributions to the genus Zodarion Walckenaer, 1826 in Turkey, with the description of a new species (Araneae: Zodariidae)
Figure 8. Zodarion kunti sp.n., SEM microphotographs, pedipalp, A. Ventral view; B. Median apophysis ventral view; C. Retrolateral view.
Figure 7 in Contributions to the genus Zodarion Walckenaer, 1826 in Turkey, with the description of a new species (Araneae: Zodariidae)
Figure 7. Zodarion kunti sp.n., ♂, pedipalp, A. Prolateral view; B. Ventral view; C. Retrolateral view (Scale 0.2).
Figure 1. Zodarion christae Bosmans, 2009 in Contributions to the genus Zodarion Walckenaer, 1826 in Turkey, with the description of a new species (Araneae: Zodariidae)
Figure 1. Zodarion christae Bosmans, 2009, habitus, ♂, A. Dorsal view; B. Ventral view; E. Ocular area frontal view; ♀, C. Dorsal view; D. Ventral view; F. Ocular area frontal view (Figures A–D Scale 1.0, Figures E–F Scale 0.5).
Figure 5 in Contributions to the genus Zodarion Walckenaer, 1826 in Turkey, with the description of a new species (Araneae: Zodariidae)
Figure 5. Zodarion kunti sp.n., ♂, habitus, A. Dorsal view; B. Ventral view; E. Lateral view; ♀, C. Dorsal view; D. Ventral view; F. Lateral view (Scale: 1.0).
Figure 2. Zodarion christae Bosmans, 2009 in Contributions to the genus Zodarion Walckenaer, 1826 in Turkey, with the description of a new species (Araneae: Zodariidae)
Figure 2. Zodarion christae Bosmans, 2009, ♂, pedipalp, A. Retrolateral view; B. Ventral view; C. Prolateral view, SEM microphotographs, D. Lateral view; E. Ventral view (Figures A–C Scale 0.5).
Figure 7 in Comparison of natural histories and karyotypes of two closely related ant-eating spiders, Zodarion hamatum and Z. italicum (Araneae, Zodariidae)
Figure 7. Behaviour of sex chromosome during spermatogonial mitosis and meiosis. (A, F) Zodarion italicum; (B– E, G–I) Z. hamatum. (A) Early spermatogonial prophase; (B) premeiotic interphase (two prominent heteropycnotic bodies represent segments of chromosome X); (C) pachytene (note that sex chromosome does not exhibit heteropycnosis); (D) late pachytene; (E) diplotene (*ring bivalent with two chiasmata); (F) metaphase I (*bivalent exhibiting precocious division); (G) anaphase I; (H) prometaphase II; (I) anaphase II. Arrow identifies sex chromosome. Scale bars: 10 mm.
Figure 4 in Comparison of natural histories and karyotypes of two closely related ant-eating spiders, Zodarion hamatum and Z. italicum (Araneae, Zodariidae)
Figure 4. Number of attacks for four ant species (pooled for females and juveniles of Zodarion italicum and Z. hamatum). For description see Figure 3.
Figure 5 in Comparison of natural histories and karyotypes of two closely related ant-eating spiders, Zodarion hamatum and Z. italicum (Araneae, Zodariidae)
Figure 5. Mimics and the putative model (from left to right): Zodarion hamatum, Lasius emarginatus and Z. italicum. Scale bar: 1 mm.
Figure 2 in Comparison of natural histories and karyotypes of two closely related ant-eating spiders, Zodarion hamatum and Z. italicum (Araneae, Zodariidae)
Figure 2. Phenology of study species. (A) Seasonal activity of adult individuals of Zodarion italicum (pitfall-trap data, n56266); (B) proportion of adults in Z. hamatum (grey bar) and Z. italicum (empty bar) during season (hand collections, n5121),? represents missing data; (C) seasonal variability in proportion of males (grey bar) and females (empty bar) of Z. italicum (pitfall-trap data, n56266).
Figure 1 in Comparison of natural histories and karyotypes of two closely related ant-eating spiders, Zodarion hamatum and Z. italicum (Araneae, Zodariidae)
Figure 1. Distribution of Zodarion hamatum and Z. italicum in Europe. Distribution of Z. italicum in southern Italy is not shown.
Figure 2 in Geographical sexual size dimorphism in an ant-eating spider, Zodarion rubidum (Araneae: Zodariidae)
Figure 2. Relationship between female prosoma size and male prosoma size (both on the log scale). Linear model was estimated using reduced major axis regression (RMA).
Figure 4 in Geographical sexual size dimorphism in an ant-eating spider, Zodarion rubidum (Araneae: Zodariidae)
Figure 4. Geographical variation of female/male prosoma size ratio in respect to the annual average temperature.
Figure 1 in Geographical sexual size dimorphism in an ant-eating spider, Zodarion rubidum (Araneae: Zodariidae)
Figure 1. Map of studied Zodarion rubidum populations. Austria: Graz; Czech Republic: Bransouze, Nepomuk, Prague; France: Perpignan, Montpellier, Les Sables; Germany: Berlin, Frankfurt am Main, Mainz, Cologne; Slovakia: Humenne´, Nováky, Sered'; Spain: Playa d'Aro.
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