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Figure 1 from: Zhao Y, Liu X-z, Bai F-y (2019) Four new species of Tremella (Tremellales, Basidiomycota) based on morphology and DNA sequence data. MycoKeys 47: 75-95. https://doi.org/10.3897/mycokeys.47.29180
Figure 1 - The maximum likelihood tree of the novel species and related taxa in Tremella sensu stricto based on the combined sequences of the nuc rDNA ITS region and nuc 28S rDNA D1/D2 domain. Bootstrap supports (BP) (> 50%) of maximum likelihood method and Bayesian posterior probability (BPP) values (> 0.9) are shown at each node. Note: ns, not supported (BP < 50% or PP < 0.9); nm, not monophyletic.
Figure 4 from: Shalimov AP, Zhu Y-M, Zhang M-H, Zhang X-C (2019) Selaginella dianzhongensis (Selaginellaceae), a new spikemoss from China. PhytoKeys 118: 75-87. https://doi.org/10.3897/phytokeys.118.30375
Figure 4 The 50% majority rule consensus tree derived from maximum likelihood showing the position of Selaginelladianzhongensis. Support values (BSML/PPBI) are shown above the main braches; the dash (–) indicates BS < 50%. The new species is shown in bold.
Figure 2 from: Shalimov AP, Zhu Y-M, Zhang M-H, Zhang X-C (2019) Selaginella dianzhongensis (Selaginellaceae), a new spikemoss from China. PhytoKeys 118: 75-87. https://doi.org/10.3897/phytokeys.118.30375
Figure 2 Selaginelladianzhongensis X.C.Zhang, sp. nov. A individual B portion of plant C habit D dorsal leaf E ventral leaf F strobili G axillary leaf H proximal surface of megaspore I distal surface of megaspores J portion of megaspore surface enlarged to show infrastructural detail K distal surface of microspore L proximal surface of microspore M portion of microspore surface enlarged to show infrastructural detail surface (Taken from Yan-Mei Zhu 8158 (PE)).
Figure 1 from: Shalimov AP, Zhu Y-M, Zhang M-H, Zhang X-C (2019) Selaginella dianzhongensis (Selaginellaceae), a new spikemoss from China. PhytoKeys 118: 75-87. https://doi.org/10.3897/phytokeys.118.30375
Figure 1 Selaginelladianzhongensis X.C.Zhang, sp. nov. A habit B adaxial view of strobilus C ventral leaf D axillary leaf E dorsal leaf F adaxial view of lower sporophyll G adaxial view of upper sporophyll H abaxial view of strobilus (Illustration made by Huixia Dong).
Figure 4 from: Hata H, Motomura H (2019) A new species of sardine, Sardinella pacifica from the Philippines (Teleostei, Clupeiformes, Clupeidae). ZooKeys 829: 75-83. https://doi.org/10.3897/zookeys.829.30688
Figure 4 Relationships of (A) pseudobranchial filament numbers, and (B) lower-jaw length (as % of standard length) to SL in Sardinellapacifica sp. n. [solid circles (solid star = holotype)] and S.fimbriata [open triangles (open star = lectotype)]
Figure 2 from: Hata H, Motomura H (2019) A new species of sardine, Sardinella pacifica from the Philippines (Teleostei, Clupeiformes, Clupeidae). ZooKeys 829: 75-83. https://doi.org/10.3897/zookeys.829.30688
Figure 2 Photograph of a stained scale, collected from mid-body below the dorsal fin, of Sardinellapacifica sp. n. (BMNH 1985.4.12.1, 105.1 mm SL, Manila Bay, Luzon Island, Philippines).
Figure 1 from: Hata H, Motomura H (2019) A new species of sardine, Sardinella pacifica from the Philippines (Teleostei, Clupeiformes, Clupeidae). ZooKeys 829: 75-83. https://doi.org/10.3897/zookeys.829.30688
Figure 1 Holotype of Sardinellapacifica sp. n., BMNH 1985.4.12.1, 105.1 mm SL, Manila Bay, Luzon Island, Philippines.
Figure 7 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 7 Scatter plot of functional odontostyle (blue square) and replacement odontostyle (white square) against body length of Lonigidoruspolyae sp. n. juveniles (J1-J4) and females (blue), and male odontostyle (red).
Figure 6 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 6 Longidoruspolyae sp. n. A–E anterior end of first- to fourth-stage juveniles and female F–J tail of first- to fourth- stage juvenile and female. Scale bar: 20 μm.
Figure 9 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 9 Phylogenetic tree using D2-D3 expansion segments of the 28S rRNA gene inferred from a Bayesian analysis with GTR+I+G model. Numbers represent the Bayesian posterior probabilities.
Figure 4 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 4 Longidoruspolyae sp. n., male A anterior region B amphidial fovea C labial region D junction of two testes E distal part of testis F sperm cells G nerve ring H, I posterior end, different magnifications J tail and spicules K supplements. Scale bars: 20 μm (A–C, F, G, J, K); 40 μm (D, E, H); 100 μm (I).
Figure 3 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 3 Longidoruspolyae sp. n., holotype A anterior end B pharyngeal region, arrows point to at nerve ring, pharyngeal bulb and cardia C intestine, posterior part with inclusions D anterior genital branch E vagina and part of the posterior genital branch F sphincter G intestine inclusion at higher magnification H tail I vagina J posterior ovary. Scale bars: 20 μm (A, F–I); 40 μm (E, J); 100 μm (B–D).
Figure 5 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 5 Longidoruspolyae sp. n. A–D anterior end of first- (J1) to fourth- (J4) stage juveniles E–H tail of first to fourth juvenile stages I variations in J1-J4 habitus shapes. Scale bars: 25 μm (A–H); 1 mm (I).
Figure 8 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 8 Bulgarian populations of Longidoruspisi Edward, Misra & Singh, 1964, anterior end of female (A) and male (B) female C, D vagina and part of reproductive system (different populations) E–G pre-rectum inclusions H labial region I vagina J–M variations in tail shape, female (J, L, M) and male (K). Populations: A, L Petrich C, E–G, M Sandanski D, H, I, J Kromidovo B, K male specimens from a tobacco field, Petrich region. Scale bars: 20 μm (A–G, J–M); 12 μm (H, I).
Figure 2 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 2 Longidoruspolyae sp. n., female A anterior region B, C variations in vagina D, E variations in tail shape F–H intestine inclusions I posterior genital branch J part of reproductive system. Scale bars: 20 μm (A–H); 100 μm (I, J).
Figure 1 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 1 Longidoruspolyae sp. n. A, B anterior region C posterior region D, J variations in tail shape E vagina F anterior genital branch G lateral pieces H, I female and male pharyngeal bulb K variations in female and male habitus shapes. Female: all except C, G and I. Scale bars: 25 μm (A–E, J, G); 50 μm (F); 1 mm (K).
Figure 10 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188
Figure 10 Phylogenetic tree using 18S rRNA gene inferred from a Bayesian analysis with GTR+I+G model. Numbers represent the Bayesian posterior probabilities.
FIGURES 75 in A new genus, Protaustrosimulium, for four species of Australian black flies (Diptera: Simuliidae)
FIGURES 75. Protaustrosimulium terebrans. Female wing (Middle Creek). Scale bar = 0.5 mm.
FIGURE 75 in Taxonomy and distribution of irregular echinoids (Echinoidea: Irregularia) from Sri Lanka
FIGURE 75. Distribution map of Nacospatangus altus recorded in this study.
Figure 3 from: Perissinotto R, Clennell L, Beinhundner G (2019) Lophorrhinides muellerae (Coleoptera, Scarabaeidae, Cetoniinae): a new genus and species from southern Tanzania. ZooKeys 833: 75-84. https://doi.org/10.3897/zookeys.833.31502
Figure 3 Known geographic distribution of Lophorrhinidesmuellerae gen. n. et sp. n. in the southern highlands of Tanzania.
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International Brain Laboratory public data
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OpenNeuro
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