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FIGURE 2 in Representativity of the genus Asphondylia Loew, 1850 (Diptera, Cecidomyiidae) in Brazil
FIGURE 2: Distribution of the number of Asphondylia species (Diptera, Cecidomyiidae) per Brazilian states. Legends: AC: Acre; AM: Amazonas; AP: Amapá; MA: Maranhão; AL: Alagoas; BA: Bahia; CE: Ceará; PB: Paraíba; TO: Tocantins; PA: Pará; RO: Roraima; PE: Pernambuco; PI: Piauí; RN: Rio Grande do Norte; SE: Sergipe; DF: Distrito Federal; GO: Goiás; MT: Mato Grosso; MS: Mato Grosso do Sul; ES: Espirito Santo; MG: Minas Gerais; RJ: Rio de Janeiro; SP: São Paulo; PR: Paraná; SC: Santa Catarina and RS: Rio Grande do Sul.
FIGURE 2. Representative Catlins Coast fossil locality photographs. 1 in Middle-Late Jurassic plant assemblages of the Catlins coast, New Zealand
FIGURE 2. Representative Catlins Coast fossil locality photographs. 1. The Chasm. Fossils are from loose blocks at the base of the cliffs. 2. Little Beach. Note tree trunk to left of rock hammer, associated with soil (arrowed) 3. Boat Harbour. Approximate location of fossil site arrowed. 4. Otara Beach. Note tree stump (arrowed).
Figure 5 in Suborders Acotylea and Cotylea (Polycladida): Study on morphological, ecological and reproductive features of some representative species from Tunisian coasts (Mediterranean)
Figure 5. Hatched juveniles and larvae in polyclads A: A twelve eyed juvenile of Leptoplana mediterranea, scale bar: 0.05 mm B: Götte's larva of Imogine mediterranea: lateral view, scale bar: 0.03 mm C: Müller's larva of Prosthiostomum siphunculus: lateral view, scale bar: 0.03 mm D: Müller's larva of Prosthiostomum siphunculus: apical view showing the three eyes (arrowheads), scale bar: 0.03 mm.
Figure 4 in Suborders Acotylea and Cotylea (Polycladida): Study on morphological, ecological and reproductive features of some representative species from Tunisian coasts (Mediterranean)
Figure 4. Copulatory apparatus in Discocelis tigrina. A: ventral view showing by transparency the ruffled pharynx (ph), the two uteri (ut), the two vasa deferentia, the common gonopore (cg), the common atrium (ca), the prostatoid organs (po) and the Lang's vesicle (Lv), scale bar: 0.5 mm. B: Section through common copulatory com; mon atrium (ca) showing prostatoid organs (po), vagina (v), uterus (ut) and vas deferens (vd) scale bar: 0.1 mm C: Diagrammatic reconstruction of copulatory apparatus. common gonopore (cg), common atrium (ca), ejaculatory duct (ed), Lang's vesicle (Lv), Penis (p) and prostatoid organs (po), scale bar: 0.1 mm.
Figure 2 in Suborders Acotylea and Cotylea (Polycladida): Study on morphological, ecological and reproductive features of some representative species from Tunisian coasts (Mediterranean)
Figure 2. Organs of attachment in Polyclads. A: ventral corrugated surface (cs) located between two genital pores of Echinoplana celerrima, scale bar: 0.2 mm. B: Genital pit (gp) in the acotylean Leptoplana mediterranea. This structure is located between the two genital pores. The two vasa deferentia (vd) unite in a common vas deferens (cvd) before entering the seminal vesicle (sv), scale bar: 0.2 mm. C. Ventral view of Prosthiostomum siphunculus showing a developed true sucker (ts) and a tubular pharynx (ph), scale bar: 1 mm.
Figure 3 in Suborders Acotylea and Cotylea (Polycladida): Study on morphological, ecological and reproductive features of some representative species from Tunisian coasts (Mediterranean)
Figure 3. Ovaries in polyclads A: Section through ovary of Echinoplana celerrima showing a ventral growing zone (grz) and a dorsal germinative zone (gmz), scale bar: 0.01 mm. B: Section through ovary of the cotylean Thysanozoon brocchii showing a ventral germinative zone (gmz) and a dorsal growing zone (grz), scale bar: 0.01 mm.
Figure 1 in Suborders Acotylea and Cotylea (Polycladida): Study on morphological, ecological and reproductive features of some representative species from Tunisian coasts (Mediterranean)
Figure 1. Anterior dorsal region in A: Echinoplana celerrima. See the tentacular (te) and cerebral eyes (ce) forming two paramedian bands, scale bar: 0.5 mm. B: Letoplana mediterranea. See clusters of tentacular (te) and cerebral eyes (ce), scale bar: 0.5 mm. C: Discocelis tigrina. Note the presence of cerebral and tentacular eyes clusters, scale bar: 0.5 mm. D: Imogine mediterranea. Note the presence of two everted nuchal tentacles (arrows), scale bar: 0.5 mm. E: Yungia aurantiaca. See the two marginal tentacles (arrows) and cerebral eyes spots (arrowhead), scale bar: 1 mm. F: Thysanozoon brocchii. Dorsal faces provided with papillae and developed marginal tentacles (arrows), scale bar: 1 mm. G: Prostheceraeus moseleyi. Note the presence of marginal tentacles (arrows) and yellow marginal line, scale bar: mm. H: Prosthiostomum siphunculus. The cerebral eyes (ce) are not included in the semi circle formed by marginal eyes (me), scale bar: 1 mm.
Figure 2. Dendrogram representing the genetic dissimilarity among the 64 P in Genetic diversity of Peltophorum dubium (Spreng.) Taub. progenies from the states of Minas Gerais and Mato Grosso do Sul, Brazil
Figure 2. Dendrogram representing the genetic dissimilarity among the 64 P. dubium progenies, obtained by average linkage clustering method and using the Euclidean distance as a measure of dissimilarity. Cophenetic correlation coefficient (0.756). Dourados/ MS, 2018-2019.
Fig. 2 Phylogenetic tree representing relationships within Discodorididae. The latter contains about 400 species and 40 in A warning for ecologists and conservation biologists using species checklists: How the European marine fauna 'lost' all of its 16 Discodoris species (Mollusca: Gastropoda)
Fig. 2 Phylogenetic tree representing relationships within Discodorididae. The latter contains about 400 species and 40 genera, only some of which are mentioned here, with special emphasis on the genera that contain species originally described in Discodoris. Tree terminal taxa are labeled with the specific epithet followed by the generic name of the original combination in parenthesis. The current generic names are given on the right side of the braces indicating the (few) species per genus mentioned. Assignment of a generic name to a clade is based on a type species that belongs to that clade (e.g., Discodoris boholiensis is the type species of Discodoris). All genera correspond to clades, with the exception of "Montereina", a metaphyletic group at the base of Discodorididae for which no autapomorphic, diagnostic features could be found. For additional information on phylogenetic analyses, authorship of species names, etc., see Dayrat (2010a)
Fig. 3 – Plots representing the 23-27 Aug 2020 in Calliptamus italicus at 3050 m: a first evidence of dispersal across the Alps? (Orthoptera: Acrididae)
Fig. 3 – Plots representing the 23-27 Aug 2020 trends of the meteorological parameters considered in order to describe the weather conditions in the days just before the observation of the female Calliptamus italicus on Punta Losetta (3050 m, Cottian Alps). The trend of each parameter is better visualized with a Loess curve (blue line; grey area = 95% confi- dence interval): a, atmospheric pressure; b, precipitations; c, wind speed (solid lines) and wind gust (dotted lines); d, wind direction (origin); e, air temperature. The data collected in each weather station are reported in different colours. Sources: ARPA Piemonte and Météo France.
Fig. 3. Representative samples from initial experiment interrupted and lef untended for 17 d in Greenhouse evaluation of neonate and adult applications of Coleomegilla maculata (Coleoptera: Coccinellidae) to control twospotted spider mite infestations
Fig. 3. Representative samples from initial experiment interrupted and lef untended for 17 d. Plants treated with lady beetles recovered from extreme stress; infested and untreated plants could not grow new leaves (no recovery).
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West) in Bumps on the back: An unusual morphology in phylogenetically distinct Peridinium aff. cinctum (= Peridinium tuberosum; Peridiniales, Dinophyceae)
◂Fig. 6 A molecular phylogeny of 56 systematically representative Peridiniaceae, including 42 accessions assignable to P. cinctum from various geographic regions. Maximum likelihood tree (– ln = 21,884.93), as inferred from a rRNA nucleotide alignment (1137 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (CZE Czech Republic, E East, GER Germany, HET Heterocapsaceae, N North, PPE Protoperidiniaceae, POL Poland, rbn ribotype n, S South, SWE Sweden, UKR Ukraine, W West)
◂Fig. 4 A molecular tree of 51 systematically representative Peridiniaceae, including all 28 accessions assignable to P. volzii. Maximum Likelihood tree (–ln = 22,017.62), as inferred from a rRNA nucleotide alignment (1,129 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (abbreviations: HET, Heterocapsaceae; PPE, Protoperidiniaceae) in Morphological and molecular variability of Peridinium volzii Lemmerm. (Peridiniaceae, Dinophyceae) and its relevance for infraspecific taxonomy
◂Fig. 4 A molecular tree of 51 systematically representative Peridiniaceae, including all 28 accessions assignable to P. volzii. Maximum Likelihood tree (–ln = 22,017.62), as inferred from a rRNA nucleotide alignment (1,129 parsimony-informative sites) and with strain number information. Numbers on branches are ML bootstrap (above) and Bayesian support values (below) for the clusters (asterisks indicate maximal support values, values under 50 and 0.90, respectively, are not shown). Clades are indicated (abbreviations: HET, Heterocapsaceae; PPE, Protoperidiniaceae)
Fig. 2 in Whole body solvent soak gives representative venom alkaloid profile from Solenopsis invicta (Hymenoptera: Formicidae) workers
Fig. 2. Gas chromatograms of hexane extracts obtained from Solenopsis invicta workers by different extraction methods. Capillary milking, gland dissection, and body without gland represent chromatograms from the sequential extraction of the same individual ants; whole body represents the chromatogram from whole body solvent-soaking extracts of 20 intact workers.
Fig. 1 in Whole body solvent soak gives representative venom alkaloid profile from Solenopsis invicta (Hymenoptera: Formicidae) workers
Fig. 1. Total ion chromatogram of whole body solvent-soaking extract of 20 intact Solenopsis invicta workers in hexane.
Рис. 5. ΔенΑрограмма меры разброса значений ΑΛя показатеΛей вΛияния опушенности и тоΛщины Λистовой пΛастинки картофеΛя на прожорΛивость Λичинок картофеΛьной коровки Fig. 5. Dendrogram representing the value scatter for the influence of pubescence and thickness of the potato leaf blade on the voracity of potato ladybug larvae in Role of potato immune factors in the trophic responses of Henosepilachna vigintioctomaculata Motschulsky, 1858
Рис. 5. ΔенΑрограмма меры разброса значений ΑΛя показатеΛей вΛияния опушенности и тоΛщины Λистовой пΛастинки картофеΛя на прожорΛивость Λичинок картофеΛьной коровки Fig. 5. Dendrogram representing the value scatter for the influence of pubescence and thickness of the potato leaf blade on the voracity of potato ladybug larvae
Рис. 2. UPGMA-ΑенΑрограмма схоΑства виΑового состава (А) и фаунистическая структура (B) сообществ земΛероек в пяти ΛокаΛитетах Амурской обΛасти: ЗЗ — Зейский заповеΑник; НЗ — Норский заповеΑник; ХЗ — Хинганский заповеΑник; ЧФЗ — ХинганоАрхаринский заказник; НБС — территория зоны вΛияния Нижнебурейской ГЭС. ΔТФ — Αревнетаежная фауна; БФ — бореаΛьная фауна; НФ — немораΛьная фауна; Αр. — преΑставитеΛи Αругих фауногенетических группировок (пояснения в тексте) Fig. 2. UPGMA dendrogram of species composition similarity (A) and fauna structure (B) of shrew communities in five Amur region localities: ZZ — Zeya nature reserve; NZ — Norsky nature reserve; KhZ — Khingansky nature reserve; ChFZ — KhinganoArkharinsky nature reserve; NBS — the area influenced by the Nizhnebureyskaya hydroelectric power station. DTP — ancient taiga fauna; BF — boreal fauna; NF — nemoral fauna; others — representatives of other faunagenetic groups (explained in the text) in Shrew species composition and fauna structure in the Norsky reserve
Рис. 2. UPGMA-ΑенΑрограмма схоΑства виΑового состава (А) и фаунистическая структура (B) сообществ земΛероек в пяти ΛокаΛитетах Амурской обΛасти: ЗЗ — Зейский заповеΑник; НЗ — Норский заповеΑник; ХЗ — Хинганский заповеΑник; ЧФЗ — ХинганоАрхаринский заказник; НБС — территория зоны вΛияния Нижнебурейской ГЭС. ΔТФ — Αревнетаежная фауна; БФ — бореаΛьная фауна; НФ — немораΛьная фауна; Αр. — преΑставитеΛи Αругих фауногенетических группировок (пояснения в тексте) Fig. 2. UPGMA dendrogram of species composition similarity (A) and fauna structure (B) of shrew communities in five Amur region localities: ZZ — Zeya nature reserve; NZ — Norsky nature reserve; KhZ — Khingansky nature reserve; ChFZ — KhinganoArkharinsky nature reserve; NBS — the area influenced by the Nizhnebureyskaya hydroelectric power station. DTP — ancient taiga fauna; BF — boreal fauna; NF — nemoral fauna; others — representatives of other faunagenetic groups (explained in the text)
Figures 8–15 in The terrestrial isopod, Cylisticus convexus (de Geer, 1778), representing a new record family in China (Oniscidea)
Figures 8–15. Male of Cylisticus convexus, CMMI 20201110002. 8. Pereopod 1. 9. Pereopod 2. 10. Pereopod 3. 11. Pereopod 4. 12. Pereopod 5. 13. Pereopod 6. 14. Pereopod 7. 15. Antenna. Scale bars = 1.0 mm.
Figures 16–24 in The terrestrial isopod, Cylisticus convexus (de Geer, 1778), representing a new record family in China (Oniscidea)
Figures 16–24. Male of Cylisticus convexus. 16–18. CMMI 20201110001. 16. Maxilliped; 17. Maxilla; 18. Maxillule. 19–20. CMMI 20201110003. 19. Right mandible; 20. Left mandible. 21–24. CMMI 20201110002. 21. pleopod 1 exopod; 22. pleopod 1 endopod; 23. pleopod 2 exopod; 24. pleopod 2 endopod. Scale bars: 16–20 = 0.5 mm; 21–24 = 1.0 mm.
Figures 1–7 in The terrestrial isopod, Cylisticus convexus (de Geer, 1778), representing a new record family in China (Oniscidea)
Figures 1–7. Male of Cylisticus convexus, CMMI 20201110002. 1. Dorsal view. 2. Ventral view. 3. Cephalon, dorsal view. 4. Telson and uropods, dorsal view. 5. Cephalon, frontal view. 6. Cephalon, ventral view. 7. Uropods, ventral view. Scale bars = 1.0 mm.
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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.