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22,710 results for “Plants for planting”
Figure 1 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 1. Secondary structure model of the SSU (18S) rRNA gene sequence of Zygaena (Mesembrynus) sarpedon lusitanica Reiss, 1936 (Lepidoptera: Zygaenidae; accession no. AJ830858) and structure variation in the helices E10-1 and E23-12 among species of the subfamily Zygaeninae. Nucleotides in the model are continuously numbered beginning at the 5′-end of the molecule; tick marks identify every tenth base. Light shading indicate helices numbered according to Wuyts et al. (2002). S1–S6 (dark shades) denote areas with variable secondary structure in the subfamily Zygaeninae. Roman numerals specify the domains I, II, III and IV. The following ambiguity code has been applied: A/C = M, C/U = Y, G/A = R.
Figure 7 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 7. Neighbour-joining tree based on structural differences in the variable areas S1–S6 (compare with Fig. 1) of the small-subunit (18S) rRNA in taxa of the genus Zygaena. The topology is rooted with Reissita simonyi and Epizygaenella caschmirensis as outgroup. Taxa of the subgenus Mesembrynus are indicated by shading. Numbers in parentheses specify the number of species in a particular group.
Figure 5 in Phylogenetic analysis of Zygaenoidea small-subunit rRNA structural variation implies initial oligophagy on cyanogenic host plants in larvae of the moth genus Zygaena (Insecta: Lepidoptera)
Figure 5. Consensus structure and base pair probability matrix of the proximal part of helix 43 (S6, Fig. 1) in Lepidoptera. Nucleotides in circles indicate consistent and/or compensatory substitutions. The size of squares in the grid is proportional to the probability of a base pairing. Note that the unpaired nucleotides C and G in the helix will most likely bind in individual structures having this specific nucleotide combination, but non-Watson–Crick pairings are too frequent in the alignment for assuming a generally nucleotide interaction at this position in the consensus structure.
Fig. 3 in Spatial pattern of a fish assemblage in a seasonal tropical wetland: effects of habitat, herbaceous plant biomass, water depth, and distance from species sources
Fig. 3. Partial regressions testing the effects of water depth (left) and distance from colonizing source (right) on fish species richness collected in 22 plots in Site of Long-Term Sampling (SLTS). Only statistically significant relationships are shown.
Fig. 1 in Spatial pattern of a fish assemblage in a seasonal tropical wetland: effects of habitat, herbaceous plant biomass, water depth, and distance from species sources
Fig. 1. Geographical location of the study area and the Site of Long-Term Sampling (in the area). The system is installed in the Pantanal, Brazil.
Fig. 1 in Effects of the proximity from an industrial plant on fish assemblages in the rio Paraíba do Sul, southeastern Brazil
Fig. 1. Study area, rio Paraíba do Sul reaches. Indication of the six sampling sites and three zones - Z I (sites 1 and 2); Z II (sites: 3 and 4); and Z III (sites 5 and 6). Buffers marked in black indicate main sources of urban and industrial pollution. Dams indicated by black line marks.
Fig. 6 in Effects of the proximity from an industrial plant on fish assemblages in the rio Paraíba do Sul, southeastern Brazil
Fig. 6. Cluster analysis of fish abundance on mode Q, showing the three zones in the Paraíba do Sul river, in 1998/99. In x-axis = 1: Z I; 2: Z II; 3: Z III.
Fig. 5 in Effects of the proximity from an industrial plant on fish assemblages in the rio Paraíba do Sul, southeastern Brazil
Fig. 5. Cluster analysis of fish abundance on mode Q, showing the three zones in the Paraíba do Sul river, in 1997/98. In x-axis = 1: Z I; 2: Z II; 3: Z III.
Fig. 4 in Effects of the proximity from an industrial plant on fish assemblages in the rio Paraíba do Sul, southeastern Brazil
Fig. 4. Number of species per geometric classes (x 2) in the three zones of the rio Paraíba do Sul, in 1997/99.
Fig. 2 in Effects of the proximity from an industrial plant on fish assemblages in the rio Paraíba do Sul, southeastern Brazil
Fig. 2. ABC curves for fish species in the three zones of the rio Paraíba do Sul, in 1997/99. Round marks - abundance; triangle marks - biomass. ABC-indexes indicated for each zone.
Fig. 3. K in Effects of the proximity from an industrial plant on fish assemblages in the rio Paraíba do Sul, southeastern Brazil
Fig. 3. K-dominance curves for the fish species in the three zones of the rio Paraíba do Sul, in 1997/99.
Figures 83–87 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 83–87. (83) P. greenwoodi head; (84) P. greenwoodi mandibles; (85) P. xanthocephalus sp. nov. head. Scale bar = 100 Mm; (86) P. greenwoodi clypeus; (87) P. xanthocephalus sp. nov. clypeus. Scale bar = 50 Mm.
Figure 94 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figure 94. Comparison of head shape between P. athysanus sp. nov. (Fig. 60) and P. proximus Wiebes (Fig. 62).
Figures 63–70 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 63–70. Antennae (females). (63) P. astrabocheilus sp. nov.; (64) P. proximus; (65) P. imperialis; (66) P. macrocainus sp. nov.; (67) P. greenwoodi; (68) P. cuneatus; (69) P. xanthocephalus sp. nov.; (70) P. athysanus sp. nov.
Figures 71–76 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 71–76. Head (females). (71) P. proximus gena; (72) P. imperialis clypeus; (73) P. macrocainus sp. nov. clypeus; (74) P. astrabocheilus sp. nov. clypeus; (75) P. athysanus sp. nov. clypeus; (76) P. proximus clypeus. Scale bar = 50 Mm.
Figures 46–52 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 46–52. (46) P. schizodontus sp. nov. pollen pocket; (47) P. rigisamos pollen pocket; (48) P. schizodontus sp. nov. tergites; (49) P. cuneatus clypeus; (50) P. cuneatus head; (51–52) P. cuneatus mandibles. Scale bar = 100 Mm.
Figures 35–39 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 35–39. Antenna (females). (35) P. nigriventris; (36) P. addicotti; (37) P. nitens; (38) P. achorus sp. nov.; (39) P. achorus sp. nov. head.
Figures 53–62 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 53–62. Head (females). (53) P. imperialis mandibles; (54) P. macrocainus sp. nov. mandibles; (55) P. proximus mandibles; (56) P. astrabocheilus sp. nov. mandibles; (57) P. imperialis head; (58) P. macrocainus sp. nov. head; (59) P. astrabocheilus sp. nov. head; (60) P. athysanus sp. nov. head; (61) P. athysanus sp. nov. mandibles and gena; (62) P. proximus head. Scale bar = 100 Mm.
Figures 9–13 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 9–13. Antennae (females). (9) P. rigisamos; (10) P. schizodontus; (11) P. froggatti; (12) P. deuterus sp. nov.; (13) P. regalis.
Figures 29–34 in Revision of the Australian species of Pleistodontes (Hymenoptera: Agaonidae) fig-pollinating wasps and their host-plant associations
Figures 29–34. Pollen pocket. (29) P. froggatti; (30) P. regalis; (31) P. deuterus sp. nov.; (32) P. nigriventris; (33) P. addicotti; (34) P. nitens. Scale bar = 50 Mm.
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.