Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
60
datasets available to search
ShareScore release 0.9.0
Dataset results
60 results for “Tetrix”
Supplementary material 3 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure S2
Figure 7 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 7 Altitudinal distribution (mean ± SD) of 286 populations of Tetrix bipunctata (green) and kraussi (orange) segmented for five Central European countries and eight Federal States in Germany. Regions are grouped along the north-south axis, NL = The Netherlands, DE = Germany: DEMV = Mecklenburg-Vorpommern, DEBB = Brandenburg, DEST = Sachsen-Anhalt, DESN = Sachsen, DETH = Thüringen, DEHE = Hessen, DEBW = Baden-Württemberg, DEBY = Bayern, AT = Austria, CH = Switzerland, IT = Italy, SL = Slovenia.
Figure 9 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 9 Vegetation cover in percent (mean ± SD) at spots of 10 cm diameter with records of adult Tetrix bipunctata and kraussi at the syntopic population at Theisa, southern Brandenburg.
Figure 5 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 5 Scatterplots of isosize against body ratios of 273 females of Tetrix bipunctata and kraussi, showing the position of intermediate specimens A isosize against ratio of hind wing length to mid-femur length, the best ratio for separation of morphs B isosize against ratio of hind wing length to tegmen length, the standard ratio for discrimination (see Fig. 4). The 11 specimens considered by Nadig (1991) as "Zwischenformen" marked by black triangles.
Figure 2 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 2 Shape principal component analysis (shape PCA) of 273 females of Tetrix bipunctata and kraussiA analysis including 17 variables, scatterplot of first against second shape PC; in parentheses the variance explained by each shape PC BPCA ratio spectrum for first shape PC CPCA ratio spectrum for second shape PC. Horizontal bars in the ratio spectra represent 68% bootstrap confidence intervals, based on 1000 replicates; only the most important characters are indicated in ratio spectra.
Figure 4 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 4 Boxplots of body ratios of 273 females of Tetrix bipunctata and kraussiA hind wing length to mid-femur length, the ratio selected by the LDA ratio extractor as the best ratio for separating the morphs B hind wing length to tegmen length, the standard ratio used for discrimination C tegmen length to hind femur length, the second best ratio found by the LDA ratio extractor (actually the best ratio when hind wing length is omitted). Means in all plots significantly different (ANOVA, p < 0.001).
Figure 8 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 8 Characteristic microhabitats of Tetrix bipunctata (left) and kraussi (right) at the syntopic population at Theisa, southern Brandenburg.
Figure 10 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 10 Vegetation height (mean ± SD) at spots of 10 cm diameter with records of adult Tetrix bipunctata and kraussi at the syntopic population at Theisa, southern Brandenburg.
Figure 1 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 1 The 20 characters measured on 273 females of Tetrix bipunctata and kraussi. Measurements indicated by yellow lines. In all cases, a single photo was taken with reference points exactly placed in the focal plane. For character definitions, see Table 1.
Figure 6 from: Moser V, Baur H, Lehmann AW, Lehmann GUC (2021) Two species? – Limits of the species concepts in the pygmy grasshoppers of the Tetrix bipunctata complex (Orthoptera, Tetrigidae). ZooKeys 1043: 33-59. https://doi.org/10.3897/zookeys.1043.68316
Figure 6 Distribution of 260 localities with records of Tetrix bipunctata (green dots), kraussi (orange dots) and syntopic populations (purple dots), mapped for six central European countries. Map generated using Natural Earth Data https://www.naturalearthdata.com/about/terms-of-use/.
Data from: Simultaneous age-dependent and age-independent sexual selection in the lekking black grouse (Lyrurus tetrix)
Individuals' reproductive success is often strongly associated with their age, with typical patterns of early-life reproductive improvement and late-life senescence. These age-related patterns are due to the inherent trade-offs between life-history traits competing for a limited amount of resources available to the organisms. In males, such trade-offs are exacerbated by the resource requirements associated with the expression of costly sexual traits, leading to dynamic changes in trait expression throughout their life span. Due to the age dependency of male phenotypes, the relationship between the expression of male traits and mating success can also vary with male age. Hence, using longitudinal data in a lekking species with strong sexual selection – the black grouse Lyrurus tetrix – we quantified the effects of age, life span and age of first lek attendance (AFL) on male annual mating success (AMS) to separate the effects of within-individual improvement and senescence on AMS from selective (dis)appearance of certain phenotypes. Then, we used male AMS to quantify univariate and multivariate sexual selection gradients on male morphological and behavioural traits with and without accounting for age and age-related effects of other traits. Male AMS increased with age, and there was no significant reproductive senescence. Most males never copulated, and of the ones that did, the majority had only one successful year. Life span was unrelated to AMS, but early AFL tended to lead to higher AMS at ages 1–3. AMS was related to most morphological and behavioural traits when male age was ignored. Accounting for age and age-specific trait effects (i.e. the interaction between a trait and age) reduced the magnitude of the selection gradients and revealed that behavioural traits are under consistent sexual selection, while sexual selection on morphological traits is stronger in old males. Therefore, sexual selection in black grouse operates primarily on male behaviour and morphological traits may act as additional cues to supplement female choice. These results demonstrate the multifaceted influence of age on both fitness and sexual traits and highlight the importance of accounting for such effects when quantifying sexual selection.
FIGURE 4 in First records of Croatian and Serbian Tetrigidae (Orthoptera: Caelifera) with description of a new subspecies of Tetrix transsylvanica (Bazyluk & Kis, 1960)
FIGURE 4. Uvarovitettix nodulosus (Fieber, 1853) from Portugal (photo: Paulo Lemos).
Figure 8 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 8 Tetrix japonica (Bolívar, 1887) A–C holotype of Tetrix cliva Zheng & Deng, 2004, syn. nov. A dorsal view B lateral view C labels D–F holotype of Tetrix duolunensis Zheng, 1996, syn. nov. D dorsal view E lateral view F labels.
Figure 15 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 15 Tetrix japonica (Bolívar, 1887). Holotype of Tetrix zhoushanensis, Gao, Liu & Yin, 2022, syn. nov. A dorsal view B lateral view (photo Gao et al.).
Figure 3 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 3 Tetrix japonica (Bolívar, 1887) A–C holotype of Coptotettix circinihumerus Zheng & Deng, 2004, syn. nov. A dorsal view B lateral view C labels D–F holotype of Coptotettix emeiensis Zheng, Lin & Zhang, 2012, syn. nov. D dorsal view E lateral view F labels.
Figure 14 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 14 Tetrix japonica (Bolívar, 1887) A–C topotype of Tetrix xinchengensis Deng, Zheng & Wei, 2007, syn. nov. A lateral view B dorsal view C labels D–F holotype of Tetrix yunlongensis Zheng & Mao, 2002, syn. nov. D lateral view E dorsal view F labels.
Figure 13 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 13 Tetrix japonica (Bolívar, 1887) A–C topotype of Tetrix ruyuanensis Liang, 1998, syn. nov. A lateral view, pronotum with nearly straight median carina B lateral view, pronotum with arcuate median carina before shoulders C dorsal view D–F holotype of Tetrix xianensis Zheng, 1996, syn. nov. D lateral view E dorsal view F labels.
Figure 5 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 5 Tetrix japonica (Bolívar, 1887) A–C holotype of Macromotettix nigritubercle Zheng & Jiang, 2006, syn. nov. A lateral view B dorsal view C labels D–F holotype of Macromotettix yaoshanensis Zheng & Jiang, 2000, syn. nov. D lateral view E dorsal view F labels.
Figure 4 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 4 Tetrix japonica (Bolívar, 1887) A–C holotype of Euparatettix rongshuiensis Zheng, 2005, syn. nov. A lateral view (The pin passes through the right side of the thorax from the shoulder of pronotum, which tends to push the pronotum down. This elevates the previously non-protruding head) B dorsal view C labels D–F holotype of Euparatettix zayuensis Zheng, Zeng & Ou, 2011, syn. nov. D lateral view (The pin passes through the right side of the thorax from the shoulder of pronotum, which tends to push the pronotum down. This elevates the previously unprotruding head) E dorsal view F labels.
Figure 2 from: Long Y, Teng C, Huang C, Zhang R, Deng W, Lin L (2023) Twenty-three new synonyms of the Eastern common groundhopper, Tetrix japonica (Bolívar, 1887) (Orthoptera, Tetrigidae). ZooKeys 1187: 135-167. https://doi.org/10.3897/zookeys.1187.110067
Figure 2 Tetrix japonica (Bolívar, 1887) A syntype, lateral view (photograph Josef Tumbrinck) B antenna, 15-segmented (including scape, pedicel, 13-segmented flagellum).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.