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Fig. 8 in P H E N O T Y P I C P L A S T I C I T Y A N D N U C L E A R D N A Polymorphism Of Two Differing Pinus Sylvestris L. Open-Pollinated Families Originating From The Same Population
Fig. 8. Unweighted pair group method (UPGMA) dendrogram based on Nei's genetic distances among investigated half-sib open-pollinated families of one Lithuanian Pinus sylvestris L. population.
Fig. 2 in P R O J E C T S O N E M Y S O R B I C U L A R I S (R E P T I L I A: Testudines: Emydidae) In Latvia For Thirty Years (1984 - 2014): Biological Aspects, Results And Effect On Population And Ecosystems
Fig. 2. Old Emys orbicularis female, found in 1984 in Daugavpils living for 20 years in a zooculture (Photo: 2005).
Fig. 6. Emys orbicularis habitat 3 in P R O J E C T S O N E M Y S O R B I C U L A R I S (R E P T I L I A: Testudines: Emydidae) In Latvia For Thirty Years (1984 - 2014): Biological Aspects, Results And Effect On Population And Ecosystems
Fig. 6. Emys orbicularis habitat 3 in Silene Nature Park after restoration (Google Earth service, SAS services).
Fig. 3 in Altitudinal Variation In Population Density, Body Size And Morphometric Structure In C A R A B U S O D O R At U S S H I L, 1996 (C O L E O P T E R A: Carabidae)
Fig. 3. Illustration of measurements: 1-2 – elytra length (hereafter "A", 3-4 – elytra width ("B"), 5-6 – pronotum length "C"), 7-8 – pronotum width (D), 9-10 – head length (E), 11–12 – distance between the eyes (signed as "head width" or "F" in the figures).
Fig. 7 in Altitudinal Variation In Population Density, Body Size And Morphometric Structure In C A R A B U S O D O R At U S S H I L, 1996 (C O L E O P T E R A: Carabidae)
Fig. 7. Descriptive statistics of elytra length means in C. odoratus at the plots on different altitudes.
Fig. 2 in Microhabitat Preference And Relationships B E T W E E N M E Ta Z O A N Pa R A S I T E S O N T H E G I L L A P Pa R At U S O F T H E E U R O P E A N E E L (A N G U I L L A Anguilla) From Freshwaters Of Latvia
Fig. 2. The metazoan parasite prevalence in different gill area of European eel Anguilla anguilla from freshwater bodies of Latvia. A – Pseudodactylogyrus bini; B – Pseudodactylogyrus anguillae; C – Ergasilus sieboldi; D – Anodonta sp.
Fig. 1 in M O L E C U L A R I D E N T I F I C A T I O N A N D Characterization Of Synanthedon Tipuliformis Clerck From Black Currant Fields
Fig. 1. Location of black currant plantations, where shoots damaged by S. typuliformis were collected.
Fig. 6 in The First Records Of The Common Pheasant, P H A S I A N U S C O L C H I C U S (Av E S: G A L L I F O R M E S: Phasianidae), And Its Group In South-Eastern Latvia
Fig. 6. The northern border of the distribution area of Phasianus colchicus in the Far East (Beme et al. 1987).
Fig. 1 in G R A I N Y I E L D A N D I T S F O R M I N G Pa R A M E T E R S Variations Of Oat Cultivars
Fig. 1. Meteorological conditions during experimental years: ■ 2012, ■ 2013, □ 2014 ■ LTA, *LTA – Long term average value of temperature 2012, 2013, 2014 Long term average value of precipitation.
Fig. 2 in The First Records Of The Common Pheasant, P H A S I A N U S C O L C H I C U S (Av E S: G A L L I F O R M E S: Phasianidae), And Its Group In South-Eastern Latvia
Fig. 2. The place of the observation of the Phasianus colchicus group. One day before: the Capreolus сapreolus have been dug last year's apples out of the snow 4 – 6 cm in depth. 2015.02.10.
Key Biodiversity Areas (KBAs) R package, KBAscope, application to Greece
<p>Key Biodiversity Areas (KBAs) represent the largest global network of sites critical to the persistence of biodiversity, which have been identified against standardised quantitative criteria. Sites that hold very high biodiversity value or potential are given specific attention on site-based conservation targets of the Kunming-Montreal Global Biodiversity Framework (GBF), and KBAs are already used in indicators for the GBF and the Sustainable Development Goals. However, most of the species that trigger KBA status are birds and to maximise benefits for biodiversity under the actions taken to fulfil the GBF, countries need to update their KBAs to represent important sites across multiple taxa. Here we introduce KBAscope, an R package to identify potential KBAs using multiple taxonomic groups. KBAscope provides flexible, user-friendly functions to edit species data (population, range maps, area of occupancy, area of habitat and localities); apply KBA criteria; and generate outputs to support the delineation and validation of KBAs. The details of the analysis - such as the spatial units tested or the KBA criteria applied - can be decided according to the scope of the analysis. We demonstrate the functionality of KBAscope by using it to identify potential KBAs in Greece based on multiple terrestrial taxonomic groups and four sizes of grid cells (4 km<sup>2</sup>, 25 km<sup>2</sup>, 100 km<sup>2</sup>, 225 km<sup>2</sup>).</p>
Figure 2. – Otolith images from a in Automatic method to transform routine otolith images for a standardized otolith database using R
Figure 2. – Otolith images from a binocular dissecting microscope under different types of illumination: A. Reflected light and B. Transmitted light.
Figure 1 in Automatic method to transform routine otolith images for a standardized otolith database using R
Figure 1. – Different types of otolith images showing common issues. Scale is different between images depending on the sample, some broken otoliths, various exposures and colors, some particles may be present (hair, bubbles).
Figure 10. – Plankton sampling aboard the R in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 10. – Plankton sampling aboard the R/V Cryos in 1975 to study herring pre-recruitment on George's Bank as part of an ICNAF project (Photo A. Forest).
Figure 6. – The R in French research on fisheries in the Northwest Atlantic, from its origins to the present
Figure 6. – The R/V Président Théodore Tissier of the Office Scien-Scien- tifique et Technique des Pêches Maritimes carried out surveys in the North West Atlantic mainly during the 1950s (source: www.lepetit-manchot.fr).
Fig. 5 in Potential herbicidal effect of synthetic chalcones on the initial growth of sesame, Sesamum indicum L., and brachiaria, Urochloa decumbens (Stapf) R. D. Webster
Fig. 5. Percentage of growth inhibition/stimulus of shoot parts of brachiaria seedlings [Urochloa decumbens (Stapf) R.D. Webster] grown for five days in water solutions containing the chalcones, or analogues, or Glyphosate®, in comparison to the positive control (distilled water). The chalcones are identified in the figure 2. *Indicates a significant difference in relation to the control, p<0.05.
Fig. 4 in Potential herbicidal effect of synthetic chalcones on the initial growth of sesame, Sesamum indicum L., and brachiaria, Urochloa decumbens (Stapf) R. D. Webster
Fig. 4. Percentage of growth inhibition/stimulus of root parts of sesame seedlings (Sesamum indicum L.) grown for five days in water solutions containing the chalcones, or analogues, or Glyphosate®, in comparison to the positive control (distilled water). The chalcones are identified in figure 2. *Indicates a significant difference in relation to the control, p<0.05.
Рис. 2. Морфотипы Зрелых сперматоЗоидов (СЭМ) у Mytilus trossulus (A–G), Crenomytilus grayanus (H–L) и Mytilus coruscus (M–R): a – акросома; br – basal ring; n – Ядро; m – митохондриЯ; fl – Жгутик. Масштаб линейки – 1 мкм. in Study on sperm heteromorphism in some mussels (Bivalvia: Mytilidae) from the Sea of Japan
Рис. 2. Морфотипы Зрелых сперматоЗоидов (СЭМ) у Mytilus trossulus (A–G), Crenomytilus grayanus (H–L) и Mytilus coruscus (M–R): a – акросома; br – basal ring; n – Ядро; m – митохондриЯ; fl – Жгутик. Масштаб линейки – 1 мкм.
◂Fig. 4 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–R light microscopy; TS in horizontal orientation). A Secantial section. B, C TS %note cellular organisation). D Secantial section. E, F TS %note cellular organisation). G Secantial section of young gynoecium showing cellular organisation. H–J TS %note lacking cellular organisation, localisation in K–M). K–M LS at different levels from outside to inside of the same specimen %note strongly stained peripheral tissue; asterisks indicate tissue illustrated in H–J). N TS %note dehiscence lines of the prospective endocarp). O, P TS showing transmission tissue and dorsal bundles at top of style. Q vascularisation at base of gynoecium %note strongly stained peripheral tissue). R Vascularisation at base of flower %LS, longisection; TS, transverse section; db, dorsal bundle; dl, dehiscent line; ep, epidermis; lb, lateral bundle; tt, transmission tissue; ut, peripheral tissue; vb, ventral bundle; vs, ventral slit) in Observations on flower and fruit anatomy in dioecious species of Cordia (Cordiaceae, Boraginales) with evolutionary interpretations
◂Fig. 4 Gynoecium of C. crenata %yellow frames), C. cf. grandicalyx %blue frames) and C. sinensis %pink frames; A–R light microscopy; TS in horizontal orientation). A Secantial section. B, C TS %note cellular organisation). D Secantial section. E, F TS %note cellular organisation). G Secantial section of young gynoecium showing cellular organisation. H–J TS %note lacking cellular organisation, localisation in K–M). K–M LS at different levels from outside to inside of the same specimen %note strongly stained peripheral tissue; asterisks indicate tissue illustrated in H–J). N TS %note dehiscence lines of the prospective endocarp). O, P TS showing transmission tissue and dorsal bundles at top of style. Q vascularisation at base of gynoecium %note strongly stained peripheral tissue). R Vascularisation at base of flower %LS, longisection; TS, transverse section; db, dorsal bundle; dl, dehiscent line; ep, epidermis; lb, lateral bundle; tt, transmission tissue; ut, peripheral tissue; vb, ventral bundle; vs, ventral slit)
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main
ScienceDex guides
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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.