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Figure 72 from: Valdez-Mondragón A, Navarro-Rodríguez CI, Solís-Catalán KP, Cortez-Roldán MR, Juárez-Sánchez AR (2019) Under an integrative taxonomic approach: the description of a new species of the genus Loxosceles (Araneae, Sicariidae) from Mexico City. ZooKeys 892: 93-133. https://doi.org/10.3897/zookeys.892.39558
Figure 72 Maximum likelihood tree inferred from the concatenated matrix (CO1 + ITS2) of Loxosceles species from Mexico. Colors of branches and bars indicate different species. Numbers above bars at right represent the delimitation methods: 1: morphology (M). 2: neighbor-joining (NJ). 3: ABGD with initial partitions (IP). 4: ABGD with recursive partitions (RP). 5: GMYC. 6: bPTP with ML. 7: bPTP with IB. Numbers below bars represent species recovered for each delimitation method. Red numbers correspond to Bayesian posterior probabilities, and black numbers are bootstrap support values from the ML analysis.
Figure 82-83 from: Valdez-Mondragón A, Navarro-Rodríguez CI, Solís-Catalán KP, Cortez-Roldán MR, Juárez-Sánchez AR (2019) Under an integrative taxonomic approach: the description of a new species of the genus Loxosceles (Araneae, Sicariidae) from Mexico City. ZooKeys 892: 93-133. https://doi.org/10.3897/zookeys.892.39558
Figure 82-83 82 Distribution records of Loxosceles tenochtitlan sp. nov. from Mexico City (CDMX), Estado de Mexico (MEX), and Tlaxcala (TLAX) 83 known records of L. tenochtitlan sp. nov. from Mexico City, including the type locality (star).
Figure 70 from: Valdez-Mondragón A, Navarro-Rodríguez CI, Solís-Catalán KP, Cortez-Roldán MR, Juárez-Sánchez AR (2019) Under an integrative taxonomic approach: the description of a new species of the genus Loxosceles (Araneae, Sicariidae) from Mexico City. ZooKeys 892: 93-133. https://doi.org/10.3897/zookeys.892.39558
Figure 70 Neighbor-joining (NJ) tree constructed from COI data of ten species of Loxosceles from Mexico. Colors of branches indicate different species. Numbers on nodes are bootstrap support values. Red circles represent Loxosceles tenochtitlan sp. nov.
Figures 23-28 from: Valdez-Mondragón A, Navarro-Rodríguez CI, Solís-Catalán KP, Cortez-Roldán MR, Juárez-Sánchez AR (2019) Under an integrative taxonomic approach: the description of a new species of the genus Loxosceles (Araneae, Sicariidae) from Mexico City. ZooKeys 892: 93-133. https://doi.org/10.3897/zookeys.892.39558
Figures 23-28 Loxosceles tenochtitlan sp. nov. Male Holotype 23–25 left palp, prolateral, dorsal and retrolateral views respectively 26–28 detail of the bulb and embolus, dorsal, retrolateral and apical views, respectively. Scale bars: 0.5 mm (23–25), 0.2 mm (26–28).
Figure 71 from: Valdez-Mondragón A, Navarro-Rodríguez CI, Solís-Catalán KP, Cortez-Roldán MR, Juárez-Sánchez AR (2019) Under an integrative taxonomic approach: the description of a new species of the genus Loxosceles (Araneae, Sicariidae) from Mexico City. ZooKeys 892: 93-133. https://doi.org/10.3897/zookeys.892.39558
Figure 71 Neighbor-joining (NJ) tree of ITS2 data of nine species of Loxosceles from Mexico. Colors of branches indicate different species. Numbers at nodes represent bootstrap support values. Red circles represent Loxosceles tenochtitlan sp. nov.
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard). in Éthologie sonore et statut acoustique de quelques Cigales thaïlandaises, incluant la description de deux espèces nouvelles (Hemiptera : Auchenorhyncha*, Cicadoidea, Cicadidae)
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard).
Figures 2-7 from: Abram PK, McPherson AE, Kula R, Hueppelsheuser T, Thiessen J, Perlman SJ, Curtis CI, Fraser JL, Tam J, Carrillo J, Gates M, Scheffer S, Lewis M, Buffington M (2020) New records of Leptopilina, Ganaspis, and Asobara species associated with Drosophila suzukii in North America, including detections of L. japonica and G. brasiliensis. Journal of Hymenoptera Research 78: 1-17. https://doi.org/10.3897/jhr.78.55026
Figures 2-7 Ganaspis brasiliensis (2, 4); Leptopilina japonica (3, 5); Pachycrepoideus vindemmiae (6); Asobara sp. (7).
Figure 1 from: Abram PK, McPherson AE, Kula R, Hueppelsheuser T, Thiessen J, Perlman SJ, Curtis CI, Fraser JL, Tam J, Carrillo J, Gates M, Scheffer S, Lewis M, Buffington M (2020) New records of Leptopilina, Ganaspis, and Asobara species associated with Drosophila suzukii in North America, including detections of L. japonica and G. brasiliensis. Journal of Hymenoptera Research 78: 1-17. https://doi.org/10.3897/jhr.78.55026
Figure 1 Map of sites where Leptopilina japonica (red circles), or both L. japonica and Ganaspis brasiliensis (green circles) were found in British Columbia, Canada in 2016 and 2019. The red box in the inset shows where the mapped area is situated in North America. Map tiles by Stamen Design, under CC BY 3.0. Data by OpenStreetMap, under ODbL.
Data from: Influences of two coexisting endosymbionts, CI-inducing Wolbachia and male-killing Spiroplasma, on the performance of their host Laodelphax striatellus (Hemiptera: Delphacidae)
The small brown planthopper Laodelphax striatellus (Hemiptera: Delphacidae) is reported to have the endosymbiont Wolbachia, which shows a strong cytoplasmic incompatibility (CI) between infected males and uninfected females. In the 2000s, female-biased L. striatellus populations were found in Taiwan, and this sex ratio distortion was the result of male-killing induced by the infection of another endosymbiont, Spiroplasma. Spiroplasma infection is considered to negatively affect both L. striatellus and Wolbachia because the male-killing halves the offspring of L. striatellus and hinders the spread of Wolbachia infection via CI. Spiroplasma could have traits that increase the fitness of infected L. striatellus and/or coexisting organisms because the coinfection rates of Wolbachia and Spiroplasma were rather high in some areas. In this study, we investigated the influences of the infection of these two endosymbionts on the development, reproduction and insecticide resistance of L. striatellus in the laboratory. Our results show that the single infection of Spiroplasma had a negative influence on the fertility of L. striatellus, while the double infection state had no significant influence. At late nymphal and adult stages, the abundance of Spiroplasma was lower in the double infection state than in the single infection state. In the double infection state, the reduction of Spiroplasma density may be caused by competition between the two endosymbionts, and the negative influence of Spiroplasma on the fertility of host may be relieved. The resistance of L. striatellus to four insecticides was compared among different infection states of endosymbionts, but Spiroplasma infection did not contribute to increased insecticide resistance. Because positive influences of Spiroplasma infection were not found in terms of the development, reproduction and insecticide resistance of L. striatellus, other factors improving the fitness of Spiroplasma-infected L. striatellus may be related to the high frequency of double infection in some L. striatellus populations.
Supplementary material 1 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Tables S1, S2
Supplementary material 3 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Dataset including amphibian species occurence information, museum specimen numbers, source of data
Figure 5 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Figure 5 Distribution records for the Hylidae family in the Equatorial Seasonally Dry Forest (SDF). In blue, the first report of Trachycephalus quadrangulum in Loja province.
Figure 4 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Figure 4 Distribution records for the Leptodactylidae family in the Equatorial Seasonally Dry Forest (SDF). In blue, distribution range extensions: for Engystomops puyango, the northernmost locality is more than 70 km from the previously known distribution; for E. randi, the first record in Peru.
Figure 6 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Figure 6 Distribution records of Ranidae and Craugastoridae in the Equatorial Seasonally Dry Forest (SDF). Maps are given for Ranidae (Lithobates bwana) and Craugastoridae (Barycholos pulcher, Pristimantis achatinus, P. lymani, P. subsigillatus, and P. walkeri).
Figure 3 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Figure 3 Distribution records of Bufonidae, Centrolenidae, Ceratophryidae and Dendrobatidae in the Equatorial Seasonally Dry Forest (SDF). Maps are given for the families Bufonidae (Rhinella alata, R. horribilis), Centrolenidae (Hyalinobatrachium tatayoi), Ceratophryidae (Ceratophrys stolzmanni) and Dendrobatidae (Epipedobates anthonyi, E. machalilla, Hyloxalus elachyhistus, H. infraguttatus). For Ceratophrys stolzmanni, blue points represent new distributional records for the species, the two southernmost localities and the highest altitude, respectively.
Figure 1 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Figure 1 Distribution of amphibian occurrence records in the Equatorial Seasonally Dry Forest (SDF). Maps are provided depending on the data source: Field data, Literature, Museum, Database.
Figure 2 from: Armijos-Ojeda D, Székely D, Székely P, Cogălniceanu D, Cisneros-Heredia DF, Ordóñez-Delgado L, Escudero A, Espinosa CI (2021) Amphibians of the equatorial seasonally dry forests of Ecuador and Peru. ZooKeys 1063: 23-48. https://doi.org/10.3897/zookeys.1063.69580
Figure 2 Amphibian species of the Equatorial Seasonally Dry Forest ARhinella alata (photo by Silvia Aldás, https://bioweb.bio) BRhinella horribilisCHyalinobatrachium tatayoiDCeratophrys stolzmanniEEpipedobates anthonyiFEpipedobates machalillaGHyloxalus elachyhistusHHyloxalus infraguttatusIBoana pellucensJBoana rosenbergiKScinax quinquefasciatusLScinax sugillatus (photograph by Santiago R. Ron, https://bioweb.bio) MScinax tsachilaNSmilisca phaeotaOTrachycephalus jordaniPTrachycephalus quadrangulumQEngystomops guayacoREngystomops montubioSEngystomops pustulatusTEngystomops puyangoUEngystomops randiVLeptodactylus labrosusWLeptodactylus melanonotusXLeptodactylus ventrimaculatusYBarycholos pulcherZPristimantis achatinusAAPristimantis lymaniABPristimantis subsigillatusACPristimantis walkeri (photograph by Santiago R. Ron, https://bioweb.bio) ADLithobates bwana. Habitat seasonal change (Reserva Ecológica Arenillas) AE april (rainy season) AF december (dry season).
Figure 3 from: Stauch KLN, Wincheski RJ, Albers J, Black TE, Reichert MS, Abramson CI (2021) Limited evidence for learning in a shuttle box paradigm in crickets (Acheta domesticus). Journal of Orthoptera Research 30(2): 155-161. https://doi.org/10.3897/jor.30.65172
Figure 3 Proportion of mean time spent on correct side of the apparatus for male crickets during each 60 s interval. Male N values: Baseline = 10, Yoked = 21, Master = 21. The bars on the data points represent the standard errors. The solid line at 0.5 indicates chance.
Figure 2 from: Stauch KLN, Wincheski RJ, Albers J, Black TE, Reichert MS, Abramson CI (2021) Limited evidence for learning in a shuttle box paradigm in crickets (Acheta domesticus). Journal of Orthoptera Research 30(2): 155-161. https://doi.org/10.3897/jor.30.65172
Figure 2 Proportion of mean time spent on correct side of the apparatus for female crickets during each 60 s interval. Female N values: Baseline = 18, Yoked = 30, and Master = 30. The bars on the data points represent the standard errors. The solid line at 0.5 indicates chance.
Figure 1 from: Stauch KLN, Wincheski RJ, Albers J, Black TE, Reichert MS, Abramson CI (2021) Limited evidence for learning in a shuttle box paradigm in crickets (Acheta domesticus). Journal of Orthoptera Research 30(2): 155-161. https://doi.org/10.3897/jor.30.65172
Figure 1 The shuttle box apparatus with propeller controller in the upper left-hand corner. In this image, one of the plexiglass covers (A) has been removed so that the shock grid can be seen more easily. In the experiments, one cricket was placed into the compartment labeled A and one cricket was placed into the compartment labeled B. A piece of filter paper was placed under the left-hand side of the shuttle box to illustrate the midpoint for the two halves of the compartment. Once the cricket was inside the compartment, the plexiglass was placed over the compartment to ensure that the cricket maintained contact with the grid.
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