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Figure 1 from: Kilian N (2012) Two new mountainous species of Lactuca (Cichorieae, Asteraceae) from Iran, one presenting a new, possibly myrmecochorous achene variant. PhytoKeys 11: 61-77. https://doi.org/10.3897/phytokeys.11.2563
Figure 1 - Lactuca denaensis – A habit, acaulescent form B–F capitula, all to the same scale, before flowering (B–D), with faded flowers (E), after flowering (F); G details of synflorescence, one capitulum at fruiting. – All from Remaudière, 5252E (IRAN 10625)
Figure 4 from: Kilian N (2012) Two new mountainous species of Lactuca (Cichorieae, Asteraceae) from Iran, one presenting a new, possibly myrmecochorous achene variant. PhytoKeys 11: 61-77. https://doi.org/10.3897/phytokeys.11.2563
Figure 4 - Distribution of Lactuca hazaranensis (circles) and the related species Lactuca rosularis (squares) and Lactuca denaensis (rhomb, actucal position as indicated by arrow), as well as of Cicerbita polyclada (triangles). – Georeferenced map based on the known collections (see Appendix and supplemented by collection cited in Kirpicznikov 1964 and Tuisl 1977) and generated with DIVA-GIS (Hijmans 2011) using an adaptation of the SRTM 90 m digital elevation data (CGIAR-CSI 2004).
Figure 3 from: Kilian N (2012) Two new mountainous species of Lactuca (Cichorieae, Asteraceae) from Iran, one presenting a new, possibly myrmecochorous achene variant. PhytoKeys 11: 61-77. https://doi.org/10.3897/phytokeys.11.2563
Figure 3 - Achenes of the Lactuca rosularis group and Cicerbita polyclada – A, F–I Lactuca hazaranensis; complete achene (A); achene after loss of easily detachable beak, dorsal view (F); ventral view (G); longitudinal section of achene showing two segments, proximal large segment with embry, distal small segment solid with yellow tissue (H); embryo (I); B Lactuca rosularis C Lactuca denaensis D–E Cicerbita polyclada, complete achene (D) and longitudinal section of distal portion showing apical cavity (E). – A–D and F–H each to the same scale A, F–I from the holotype at IRAN B from Rechinger 55980 B, C from Kotschy 662 (B 100426936) D–E from Strauss 14091 (B 100312952)
Figure 1 from: Brunke A, Klimaszewski J, Anderson R (2012) Present taxonomic work on Staphylinidae (Coleoptera) in Canada: progress against all odds. ZooKeys 186: 1-5. https://doi.org/10.3897/zookeys.186.3252
Figure 1 - Level of taxonomic maturity and approximate number of species in Canadian Staphylinidae subfamilies: '0' denotes mostly unrevised subfamilies; '1' denotes maturing subfamilies with some modern revisionary works; '2' denotes nearly mature subfamilies with modern revisions for most or all genera; '3' denotes mature subfamilies post modern revision, with reviews and keys available in some format. *Phloeocharinae is ranked here as nearly mature because current keys do not separate the recently introduced Phloeocharis subtilissima Mannerheim from all native members of the subfamily.
Figure 4 from: Baker E, Johnson K, Young J (2011) The future of the past in the present: biodiversity informatics and geological time. ZooKeys 150: 397-405. https://doi.org/10.3897/zookeys.150.2350
Figure 4 - An example Sample record from IPAEG showing user-linked/edited age ranges (above) and calculated union and intersection dates (below).
Figure 1 from: Fedorova LI, Kaygorodova IA (2016) The present state of the leech fauna (Annelida, Hirudinea) in the Upper Irtysh cascade of water reservoirs. ZooKeys 596: 1-12. https://doi.org/10.3897/zookeys.596.7886
Figure 1 - Geographical location of the study region with indication of sampling areas: 1 Shulbinsk water reservoir 2 Bukhtarma water reservoir.
Figure 2 from: Fedorova LI, Kaygorodova IA (2016) The present state of the leech fauna (Annelida, Hirudinea) in the Upper Irtysh cascade of water reservoirs. ZooKeys 596: 1-12. https://doi.org/10.3897/zookeys.596.7886
Figure 2 - External morphology of new species from the Upper Irtysh reservoirs: A Alboglossiphonia sp. B Erpobdella sp. C Piscicola sp. 1 D Piscicola sp. 2. Scale bar is 5 mm.
Figure 1 from: Dimitriou AC, Taiti S, Schmalfuss H, Sfenthourakis S (2018) A molecular phylogeny of Porcellionidae (Isopoda, Oniscidea) reveals inconsistencies with present taxonomy. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 163-176. https://doi.org/10.3897/zookeys.801.23566
Figure 1 Dated phylogram based on concatenated data set including five genes (COI, 16s, 18s, 28s, NAK), generated using a relaxed lognormal clock in BEAST. BI posterior probabilities (>0.9) and ML bootstrap values (>60) are presented above the nodes. Estimated mean divergence time is given below the nodes only where nodes are statistically supported or the topology was identical between BI, ML and BEAST analyses. Subclades including individuals from more than one species have been collapsed to genus level, since all (except Porcellio) were monophyletic. Abbreviations: P. Porcellionidae, T. Trachelipodidae, A. Agnaridae, R. Armadillidiidae. Numbers in parentheses after each taxon name refer to numbering of taxa in Table 1.
Fig 4 from: Riede K (2018) Acoustic profiling of Orthoptera: present state and future needs. Journal of Orthoptera Research 27(2): 203-215. https://doi.org/10.3897/jor.27.23700
Fig 4 A data warehouse for sound management. The scheme illustrates elements and workflow for acoustic profiling of Orthoptera. Songs are sampled either by recording individual songsters (Targeted Recordings), or entire acoustic scenes, each of which could contain several Orthoptera songs. Targeted recordings are treated like specimens, with time and locality stamps and, preferably, a voucher specimen. All databases listed in Table 1 are designed to store individual recordings. These distributed databases could be federated via ABCD- or Darwin-protocol. Soundscapes require distinct data management of large multimedia files. Orthoptera songs could be extracted manually or semi-automatically as sound snippets, and eventually be identified (ID) manually, or using automatic sound recognition algorithms (ASR). Many snippets can be extracted from each scene, resulting in a one-to-many relationship between scenes and snippets.
Fig 2 from: Riede K (2018) Acoustic profiling of Orthoptera: present state and future needs. Journal of Orthoptera Research 27(2): 203-215. https://doi.org/10.3897/jor.27.23700
Fig 2 The SYSTAX database. Screenshot of the new SYSTAX user interface, to be released under www.systax.org. A search for the Neotropical tettigoniid genus Anaulacomera recovers several sound recordings from a voucher specimen of a hitherto undescribed species, documented by photographs. Faceting allows searching by images or sounds exclusively.
Fig 1 from: Riede K (2018) Acoustic profiling of Orthoptera: present state and future needs. Journal of Orthoptera Research 27(2): 203-215. https://doi.org/10.3897/jor.27.23700
Fig 1 Web-based sound analysis tool for the Macaulay Sound Library, Cornell Lab (https://www.macaulaylibrary.org). Macaulay Library provides more than 400,000 playable audio files (http://macaulaylibrary.org/index.do), and even permits spectrographic online visualization using RavenViewer as a free browser plugin (http://www.birds.cornell.edu/brp/software/sound-analysis-tools). The example shows a recording of a Virtuoso katydid by T. Walker, who provided most of the Orthoptera sound recordings for this sound library. For further details, see text.
Fig 3 from: Riede K (2018) Acoustic profiling of Orthoptera: present state and future needs. Journal of Orthoptera Research 27(2): 203-215. https://doi.org/10.3897/jor.27.23700
Fig 3 Embedding metadata within sound files. Metadata were embedded within wav and mp3 fields directly from the SYSTAX database using Soundminer software (http://store.soundminer.com/). Metadata are visible within most mp3-players, displaying the species name as "TrackTitle" and the recordist as "Artist" (Courtesy: S. Ingrisch).
Fig. 6 in A new genus and species of Polynoidae (Annelida: Polychaeta) from the Canary Islands, and update on taxa present in the Northeast Atlantic
Fig. 6. Webbnesia maculata gen. et sp. nov., holotype (TFMCBM-AN/246). A. Notochaetae. B. Upper, middle and lower neurochaetae. C. Distal part of upper and middle neurochaetae. D. Distal part of lower neurochaetae. Scale bar: A, C–D = 40 µm; B = 20 µm.
Fig. 3 in A new genus and species of Polynoidae (Annelida: Polychaeta) from the Canary Islands, and update on taxa present in the Northeast Atlantic
Fig. 3. Webbnesia maculata gen. et sp. nov., holotype (TFMCBM-AN/246). A. Complete specimen, dorsal view. B. Anterior end, dorsal view. C. Complete specimen, ventral view. D. Posterior end, ventral view. Scale bar: A, C = 2 mm; B = 0.6 mm; D = 0.8 mm.
Fig. 4 in A new genus and species of Polynoidae (Annelida: Polychaeta) from the Canary Islands, and update on taxa present in the Northeast Atlantic
Fig. 4. Webbnesia maculata gen. et sp. nov., holotype (TFMCBM-AN/246). A. Left elytron of segment 21. B. Elytral margin with part of pigmented patch. C. Eggs within parapodium. D. Right cirrigerous parapodium of segment 20, with eggs in basal part. Scale bar: A = 1.6 mm; B–C = 200 µm; D = 0.5 mm.
FIGURE 8 in The life history of Hayesiana triopus (Westwood, 1847), with taxonomic notes on both present and former species of the genus Hayesiana Fletcher, 1982 (Lepidoptera: Sphingidae)
FIGURE 8. Female genitalia of Dahira farintaenia from Hanzhong County, Shaanxi. Scale bar = 1 mm.
Supplementary material 3 from: Rodrigues-Filho SJM, dos Santos Lobato F, Medeiros de Abreu CH, Rebelo MT (2023) Where in Europe is Chrysomya albiceps? Modelling present and future potential distributions. NeoBiota 85: 81-99. https://doi.org/10.3897/neobiota.85.96687
Supplementary information
Fig. 2 in An overview of acyclotides: Past, present and future
Fig. 2. Proportion of acyclotides and cyclotides in six angiosperm families.
Spectra and light curves presented in Double detonations: variations in Type Ia supernovae due to different core and He shell masses – II. Synthetic observables
<p>Dataset containing simulated spectra and light curves presented in the paper "Double detonations: variations in Type Ia supernovae due to different core and He shell masses – II. Synthetic observables" (<a href="https://ui.adsabs.harvard.edu/abs/2022MNRAS.517.5289C/abstract">ADS</a>).</p> <p> </p>
Magnetic Fabric of Freshly Consolidated Lacustrine Mudstones Constrains the "Present-Day" Strain Field
<p>Paper data storage</p>
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.