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Figure 9 from: Wang L, Chen J-z, Dong Z-m, Chen G-w, Sluys R, Liu D-z (2021) Two new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the tropical monsoon forest in southern China. ZooKeys 1059: 89-116. https://doi.org/10.3897/zookeys.1059.65633
Figure 9 Habitat and external appearance of Dugesia verruculaA sampling site B habitat C sexually mature living individual (ca. 50 days old). Abbreviations: coa: copulatory apparatus; e: eye; ph: pharynx. Scale bar: 5 mm.
Supplementary material 2 from: Wang L, Chen J-z, Dong Z-m, Chen G-w, Sluys R, Liu D-z (2021) Two new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the tropical monsoon forest in southern China. ZooKeys 1059: 89-116. https://doi.org/10.3897/zookeys.1059.65633
Table S1
Supplementary material 1 from: Wang L, Chen J-z, Dong Z-m, Chen G-w, Sluys R, Liu D-z (2021) Two new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the tropical monsoon forest in southern China. ZooKeys 1059: 89-116. https://doi.org/10.3897/zookeys.1059.65633
Figure S1
Figure 8 from: Wang L, Chen J-z, Dong Z-m, Chen G-w, Sluys R, Liu D-z (2021) Two new species of Dugesia (Platyhelminthes, Tricladida, Dugesiidae) from the tropical monsoon forest in southern China. ZooKeys 1059: 89-116. https://doi.org/10.3897/zookeys.1059.65633
Figure 8 Dugesia circumcisa Sagittal reconstruction of the copulatory apparatus of paratype YWSZ9. Abbreviations: bc: bursal canal; cb: copulatory bursa; cg: cement glands; d1: first diaphragm; d2: second diaphragm; ed: ejaculatory duct; go: gonopore; lod: left oviduct; lvd: left vas deferens; no: nozzle; pg: penial glands; pp: penis papilla; rod: right oviduct; rvd: right vas deferens; sg: shell glands; sv: seminal vesicle. Scale bar: 100 μm.
Figure 6 from: Feng X-X, Xiao Y, Liu Z-X, Li R-K, Wei D, Tian D-K (2021) Begonia pseudoedulis, a new species in Begonia sect. Platycentrum (Begoniaceae) from southern Guangxi of China. PhytoKeys 182: 113-124. https://doi.org/10.3897/phytokeys.182.69074
Figure 6 B. edulis (A–J) and B. dielsiana (K–O) for comparison to B. pseudoedulisA habitat B, C leaf blade (adaxial and abaxial) D inflorescence E staminate flower F, G pistillate flowers H ovary & stigma I cross-section of ovary J immature capsule K habitat L staminate flowers M androecium N pistillate flowers O cross-section of ovary.
Figure 5 from: Feng X-X, Xiao Y, Liu Z-X, Li R-K, Wei D, Tian D-K (2021) Begonia pseudoedulis, a new species in Begonia sect. Platycentrum (Begoniaceae) from southern Guangxi of China. PhytoKeys 182: 113-124. https://doi.org/10.3897/phytokeys.182.69074
Figure 5 Bayesian inference of the phylogenetic position of the newly described B. pseudoedulis within sect. Platycentrum based on nuclear ITS sequences.
Figure 3 from: Feng X-X, Xiao Y, Liu Z-X, Li R-K, Wei D, Tian D-K (2021) Begonia pseudoedulis, a new species in Begonia sect. Platycentrum (Begoniaceae) from southern Guangxi of China. PhytoKeys 182: 113-124. https://doi.org/10.3897/phytokeys.182.69074
Figure 3 Variation in leaf morphology of different populations of Begonia pseudoedulisA–E the population from Fangcheng, Fangchenggang, Guangxi (A, B mature plants C–E juvenile individuals showing dense hairs on petioles) F–H wuming, Nanning, Guangxi I, J daxin, Chongzuo, Guangxi (photos A–E, J by Dai-Ke Tian F–H by Jun Liu from Zhejiang University; I by Chen-Yang Zhao from Daxin County of Guangxi). Note: The population from Daxin, Chongzuo (I, J) is only recognized by morphology without molecular evidence.
Figure 2 from: Feng X-X, Xiao Y, Liu Z-X, Li R-K, Wei D, Tian D-K (2021) Begonia pseudoedulis, a new species in Begonia sect. Platycentrum (Begoniaceae) from southern Guangxi of China. PhytoKeys 182: 113-124. https://doi.org/10.3897/phytokeys.182.69074
Figure 2 Habitat and morphology of Begonia pseudoedulisA habitat B creeping rhizome C stipule D petiole showing hairs E mature leaf blade (adaxial) F juvenile leaf blade (adaxial) G, H mature leaf blade (abaxial) I inflorescence J bracts K erect stem at anthesis L front view of staminate flower M back view of staminate flower N stamens O front view of pistillate flower P back view of pistillate flower Q ovary with styles and stigmas R cross section of ovary S, T Immature capsule (different views) U dry capsule showing abaxial wing V dry capsule showing lateral wings.
Figure 1 from: Feng X-X, Xiao Y, Liu Z-X, Li R-K, Wei D, Tian D-K (2021) Begonia pseudoedulis, a new species in Begonia sect. Platycentrum (Begoniaceae) from southern Guangxi of China. PhytoKeys 182: 113-124. https://doi.org/10.3897/phytokeys.182.69074
Figure 1 Begonia pseudoedulisA habitat B adaxial leaf blade C abaxial leaf blade D, E inflorescences F staminate flower (abaxial) G staminate flower (adaxial) H stamen I pistillate flower (adaxial) J pistillate flower (abaxial) K ovary and stigma L cross section of ovary M capsule (Illustration drawn by Yunxiao Liu).
Figure 7C- D from: Mesibov R (2011) A remarkable case of mosaic parapatry in millipedes. ZooKeys 156: 71-84. https://doi.org/10.3897/zookeys.156.1893
Figure 7C- D - Figure 7C, D. Centroids from Fig. 6 superimposed on simplified bedrock geology C and mean annual rainfall isohyets, in mm D. In C, colours crossed by main parapatric boundary represent (anticlockwise from top left) Quaternary coastal sand and gravel (gray-blue), Precambrian siltstone and mudstone (orange), Precambrian metamorphics (green), Cambrian conglomerate and siltstone (gray-green), Tertiary basalt (light brown) and Permian glaciomarine sedimentary rocks (red-brown). Scale bars = 25 km.
Figure 3 from: Deans A, Seltmann K, Yoder M, Miko I, Forshage M, Bertone M, Agosti D, Austin A, Balhoff J, Borowiec M, Brady S, Broad G, Brothers D, Burks R, Buffington M, Campbell H, Dew K, Ernst A, Fernandez-Triana J, Gates M, Gibson G, Jennings J, Johnson N, Karlsson D, Kawada R, Krogmann L, Kula R, Ohl M, Rasmussen C, Ronquist F, Schulmeister S, Sharkey M, Talamas E, Tucker E, Vilhelmsen L, Ward P, Wharton R (2012) A hymenopterists' guide to the Hymenoptera Anatomy Ontology: utility, clarification, and future directions. Journal of Hymenoptera Research 27: 67-88. https://doi.org/10.3897/jhr.27.2961
Figure 3 - The detailed breakdown report from an analyzer report. See Using the "analyzer" tool for explanation.
Figure 2 from: Deans A, Seltmann K, Yoder M, Miko I, Forshage M, Bertone M, Agosti D, Austin A, Balhoff J, Borowiec M, Brady S, Broad G, Brothers D, Burks R, Buffington M, Campbell H, Dew K, Ernst A, Fernandez-Triana J, Gates M, Gibson G, Jennings J, Johnson N, Karlsson D, Kawada R, Krogmann L, Kula R, Ohl M, Rasmussen C, Ronquist F, Schulmeister S, Sharkey M, Talamas E, Tucker E, Vilhelmsen L, Ward P, Wharton R (2012) A hymenopterists' guide to the Hymenoptera Anatomy Ontology: utility, clarification, and future directions. Journal of Hymenoptera Research 27: 67-88. https://doi.org/10.3897/jhr.27.2961
Figure 2 - Using and interpreting results from the analyzer. See Using the "analyzer" tool for explanation. A Help link B Input field C CAPTCHA test D Result table E Download link; and F Detailed breakdown link.
Figure 1 from: Cordaux R, Pichon S, Ben Afia Hatira H, Doublet V, Grève P, Marcadé I, Braquart-Varnier C, Souty-Grosset C, Charfi-Cheikhrouha F, Bouchon D (2012) Widespread Wolbachia infection in terrestrial isopods and other crustaceans. ZooKeys 176: 123-131. https://doi.org/10.3897/zookeys.176.2284
Figure 1 - Phylogenetic tree of B-supergroup Wolbachia strains based on wsp sequences, using Minimum Evolution analysis. The tree is rooted with two A-supergroup Wolbachia strains. Bootstrap values inferred from 1000 replicates are shown as percentages. Strains are identified by the host species from which they were isolated. Wolbachia strains from terrestrial isopods and non terrestrial isopod crustaceans are shown in blue and red, respectively. New crustacean Wolbachia infections reported in this study are underlined. Wolbachia strains from insects are shown in black. Names assigned to groups of Wolbachia strains are shown on the right, following Cordaux et al. (2001).
Figure 1b from: Kotze D, Brandmayr P, Casale A, Dauffy-Richard E, Dekoninck W, Koivula M, Lovei G, Mossakowski D, Noordijk J, Paarmann W, Pizzoloto R, Saska P, Schwerk A, Serrano J, Szyszko J, Taboada Palomares A, Turin H, Venn S, Vermeulen R, Zetto Brandmayr T (2011) Forty years of carabid beetle research in Europe – from taxonomy, biology, ecology and population studies to bioindication, habitat assessment and conservation. ZooKeys 100: 55-148. https://doi.org/10.3897/zookeys.100.1523
Figure 1b - Front covers of the first European meetings, ECM 1–8 and that of Hamburg 1984 (centre cover) (see also Table 2).
Figure 2 from: Kotze D, Brandmayr P, Casale A, Dauffy-Richard E, Dekoninck W, Koivula M, Lovei G, Mossakowski D, Noordijk J, Paarmann W, Pizzoloto R, Saska P, Schwerk A, Serrano J, Szyszko J, Taboada Palomares A, Turin H, Venn S, Vermeulen R, Zetto Brandmayr T (2011) Forty years of carabid beetle research in Europe – from taxonomy, biology, ecology and population studies to bioindication, habitat assessment and conservation. ZooKeys 100: 55-148. https://doi.org/10.3897/zookeys.100.1523
Figure 2 - Different pitfall types. A = Jar or yoghurt can. B and C = traps with an outer can to make collecting of the sample easier. B = funnel trap with small jar. C = trap for moist biotopes (the outer can contains gravel or stones to prevent the can from being pushed up by groundwater). V = preservative (usually formaldehyde 3–4% or propylene glycol), S = stones or gravel.
Figure 1a from: Kotze D, Brandmayr P, Casale A, Dauffy-Richard E, Dekoninck W, Koivula M, Lovei G, Mossakowski D, Noordijk J, Paarmann W, Pizzoloto R, Saska P, Schwerk A, Serrano J, Szyszko J, Taboada Palomares A, Turin H, Venn S, Vermeulen R, Zetto Brandmayr T (2011) Forty years of carabid beetle research in Europe – from taxonomy, biology, ecology and population studies to bioindication, habitat assessment and conservation. ZooKeys 100: 55-148. https://doi.org/10.3897/zookeys.100.1523
Figure 1a - Participants of the first European Carabidologist Meeting in Wijster, 1969. From left to right: Vlijm, Van der Aart, Lindroth, Stein, Wijmans, Hengeveld, Palmén, Van Dijk, Richter, Venema, Mook, Thiele, Tjallingii, Den Boer, Haeck, Neumann, Meijer.
Figure 1c from: Kotze D, Brandmayr P, Casale A, Dauffy-Richard E, Dekoninck W, Koivula M, Lovei G, Mossakowski D, Noordijk J, Paarmann W, Pizzoloto R, Saska P, Schwerk A, Serrano J, Szyszko J, Taboada Palomares A, Turin H, Venn S, Vermeulen R, Zetto Brandmayr T (2011) Forty years of carabid beetle research in Europe – from taxonomy, biology, ecology and population studies to bioindication, habitat assessment and conservation. ZooKeys 100: 55-148. https://doi.org/10.3897/zookeys.100.1523
Figure 1c - Front covers of the last five ECMs and of a few major carabidology publications (Thiele 1977; Ball et al. 1998; Erwin et al. 1979; Noonan et al. 1992) (see also Table 2).
Figure 1 from: Haston E, Cubey R, Pullan M, Atkins H, Harris D (2012) Developing integrated workflows for the digitisation of herbarium specimens using a modular and scalable approach. ZooKeys 209: 93-102. https://doi.org/10.3897/zookeys.209.3121
Figure 1 - Diagrammatic overview of the digitisation workflows at the Royal Botanic Garden Edinburgh (RBGE)
Figure 5 from: Bloom D, Thomer A, Vaidya G, Guralnick R, Russell L (2012) From documents to datasets: A MediaWiki-based method of annotating and extracting species observations in century-old field notebooks. ZooKeys 209: 235-253. https://doi.org/10.3897/zookeys.209.3247
Figure 5 - An example of how a location (Big Thompson Creek near Loveland), a date (Sunday, June 10, 1906), and a taxon (Cottonwood, genus Populus) are grouped from across multiple pages.
Figure 4 from: Bloom D, Thomer A, Vaidya G, Guralnick R, Russell L (2012) From documents to datasets: A MediaWiki-based method of annotating and extracting species observations in century-old field notebooks. ZooKeys 209: 235-253. https://doi.org/10.3897/zookeys.209.3247
Figure 4 - Editing a notebook page on Wikisource. This screenshot shows side-by-side transcription and wiki markup syntax.
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.