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Figure 17 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 17 Epigynes of Neoscona theisi (A–C), N. spasskyi (D–F) and N. isatis sp. nov. (G–I). A, D, G Ventral B, E, H posterior C, F, I lateral. Abbreviations: Le lateral extension, Sc scape. Scale bars: 0.2 mm.
Figure 16 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 16 SEM graphs of the bulbs of Neoscona spasskyi (A–C) and N. isatis sp. nov. (D–F). A, C, D, F Prolateral B, E anterior. Abbreviations: Co conductor, Em embolus, La lamella, Ma median apophysis, Ms spur of median apophysis, Sm stipes of median apophysis, Ta terminal apophysis. Scale bars: 0.1 mm.
Figure 14 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 14 Male palps and tibiae II of Neoscona theisi (A, D), N. isatis sp. nov. (B, F) and N. spasskyi (C, E). A–C Male palp, prolateral D–F male tibia II, ventral. Abbreviations: Co conductor, La lamella, Ma median apophysis, Me extension of median apophysis, Ta terminal apophysis, Te tegulum. Scale bars: 0.2 mm, unless stated otherwise.
Figure 13 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 13 Females of Neoscona theisi (A, B), N. spasskyi (C, D) and N. isatis sp. nov. (E, F). A, C, E Prosoma, ventral B, D, F abdomen, ventral. Photos A, B courtesy of A. Seropian.
Figure 12 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 12 Habitus of Neoscona spasskyi (A, B) and N. theisi (C, D). A–C Dorsal D ventral C, D showing variations in comparison to specimens depicted in Figure 11. Photos C, D courtesy of A. Seropian.
Figure 11 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 11 Dorsal habitus of Neoscona theisi (A, B), N. spasskyi (C) and N. isatis sp. nov. (D, E). A, C, D Females B, E males.
Figure 10 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 10 Lateral view of epigynes of Araniella villanii sp. nov. (A), A. proxima (B), A. mithra sp. nov. (C) and A. opisthographa (D). Scale bars: 0.2 mm.
Figure 1 from: Zamani A, Marusik YM, Šestáková A (2020) On Araniella and Neoscona (Araneae, Araneidae) of the Caucasus, Middle East and Central Asia. ZooKeys 906: 13-40. https://doi.org/10.3897/zookeys.906.47978
Figure 1 Dorsal habitus of Araniella mithra sp. nov. (A, C) and A. villanii sp. nov. (B, D) and abdomen of A. nigromaculata (E). A, B Males C, D females. Blue triangles point on black dots on opisthosoma. Scale bars: 1 mm.
Supplementary material 4 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
The relationships between body length and buccal tube length in Milnesium reductum
Supplementary material 1 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
The relationships between body length and buccal tube length in Milnesium berladnicorum
Figure 4 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Figure 4 The morphology of Milnesium reductum Tumanov, 2006 A Habitus of adult female, PCM; B SEM photograph of mouth opening; with six, unequal in size peribuccal lamellae, so-called 4+2 configuration; C SEM photograph of smooth dorsal cuticle with visible single, complex pseudoplate; D smooth dorsal cuticle, with visible single pseudoplate and faint pseudopores, specimen from KG.013 population, PCM; E smooth dorsal cuticle, with visible single pseudoplate and faint pseudopores, paratype, PCM. All the scale bars are given in µm.
Supplementary material 2 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Matrix of Milnesium reductum genetic distances
Supplementary material 3 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
The relationships between body length and buccal tube length in Milnesium almatyense
Figure 6 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Figure 6 Fragment of the Bayesian phylogenetic tree ("clade A"), based on the analysis of concatenated 18S rRNA + 28S rRNA + ITS-2 + COI nucleotide sequences, obtained by Morek and Michalczyk (2020) with an addition of six new populations, showing the positions of the two Milnesium species analysed in this contribution (shaded in grey): M. almatyense Tumanov, 2006 and M. reductum Tumanov, 2006. The numbers at nodes represent Posterior Probability (PP) supports, with the values in grey font indicating poor support (conventionally recognised as polytomy). The scale bar shows the number of substitutions per site. For the remaining parts of the tree, please see Morek and Michalczyk (2020).
Figure 5 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Figure 5 The morphology of claws of Milnesium reductum Tumanov, 2006 A Photograph of hatchlings claws III with a [2-2] CC, PCM; B Photograph of hatchlings claws IV with a [2-2] CC, PCM; C SEM photograph of claws II with a [2-3] CC lacking accessory points; D SEM photograph of tip of primary branch of claws lacking accessory points. All the scale bars are given in µm.
Figure 3 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Figure 3 The morphology of Milnesium almatyense Tumanov, 2006 adults cuticle. A Sculptured dorsal cuticle, with visible pseudoplates, specimen from KZ.003 population, PCM; B Sculptured dorsal cuticle, with visible pseudoplates, paratype, PCM; C Dorsal cuticle with visible pseudopores, the same specimens on A from KZ.003 population, PCM; D Dorsal cuticle with visible pseudopores, paratype, PCM. E SEM photograph of dorsal cuticle with visible sculpture and caudal, complex pseudoplate. F SEM photograph of details of sculpture of the dorsal cuticle. The photographs A and C, as well as B and D depict the same specimen and paratype, respectively. All the scale bars are given in µm.
Figure 2 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Figure 2 The morphology of Milnesium almatyense Tumanov, 2006 adults. A Habitus, PCM; B The pseudoplate arrangement based on adult specimens from population KZ.003, drawing; C SEM photograph of mouth opening; with six, unequal in size peribuccal lamellae, so-called 4+2 configuration; D SEM photograph of claws II with a [2-3] CC and visible accessory points. All the scale bars are given in µm.
Figure 1 from: Morek W, Surmacz B, Michalczyk Ł (2020) Novel integrative data for two Milnesium Doyère, 1840 (Tardigrada: Apochela) species from Central Asia. Zoosystematics and Evolution 96(2): 499-514. https://doi.org/10.3897/zse.96.52049
Figure 1 The morphology of Milnesium almatyense Tumanov, 2006 hatchlings, PCM. A Habitus; B Claws II, with the [2-2] CC; C Dorsal cuticle with visible sculpture in form of reticulation. All the scale bars are given in µm.
Data from: A grazing Gomphotherium in Middle Miocene Central Asia, 10 million years prior to the origin of the Elephantidae
Feeding preference of fossil herbivorous mammals, concerning the coevolution of mammalian and floral ecosystems, has become of key research interest. In this paper, phytoliths in dental calculus from two gomphotheriid proboscideans of the middle Miocene Junggar Basin, Central Asia, have been identified, suggesting that Gomphotherium connexum was a mixed feeder, while the phytoliths from G. steinheimense indicates grazing preference. This is the earliest-known proboscidean with a predominantly grazing habit. These results are further confirmed by microwear and isotope analyses. Pollen record reveals an open steppic environment with few trees, indicating an early aridity phase in the Asian interior during the Mid-Miocene Climate Optimum, which might urge a diet remodeling of G. steinheimense. Morphological and cladistic analyses show that G. steinheimense comprises the sister taxon of tetralophodont gomphotheres, which were believed to be the general ancestral stock of derived "true elephantids"; whereas G. connexum represents a more conservative lineage in both feeding behavior and tooth morphology, which subsequently became completely extinct. Therefore, grazing by G. steinheimense may have acted as a behavior preadaptive for aridity, and allowing its lineage evolving new morphological features for surviving later in time. This study displays an interesting example of behavioral adaptation prior to morphological modification.
FIGURE 2 in Notes on Docosia Winnertz (Diptera: Mycetophilidae), with description of six new species from Central Asia and the first generic record from the Afrotropical region
FIGURE 2. Habitus photo of Docosia chimganica sp. nov., holotype. Scale bar = 1mm.
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