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644 results for “Shrubs”
Figure 7 from: Vargas HA (2024) On Ypsolopha micromoths (Lepidoptera, Ypsolophidae) associated with Adesmia shrubs (Fabaceae) in the arid western slope of the central Andes. ZooKeys 1195: 131-138. https://doi.org/10.3897/zookeys.1195.116134
Figure 7 Neighbor-joining tree of DNA barcodes of the genus Ypsolopha Latreille, 1796 (Lepidoptera, Ypsolophidae) from the Andes of northern Chile. Stars and squares indicate specimens of Ypsolopha moltenii Vargas, 2018 collected on Adesmia atacamensis Meyen and Adesmia verrucosa Meyen (Fabaceae), respectively. Numbers near branches indicate bootstrap support (1,000 replicates).
Figures 5- 6 from: Vargas HA (2024) On Ypsolopha micromoths (Lepidoptera, Ypsolophidae) associated with Adesmia shrubs (Fabaceae) in the arid western slope of the central Andes. ZooKeys 1195: 131-138. https://doi.org/10.3897/zookeys.1195.116134
Figures 5- 6 Micromoths of the genus Ypsolopha Latreille, 1796 (Lepidoptera, Ypsolophidae) from the Andes of northern Chile, representing new host records of the South American genus Adesmia DC. (Fabaceae) 5 male of Ypsolopha moltenii Vargas, 2018 reared from larvae collected on Adesmia atacamensis Phil., dorsal view, abdomen removed 6 male of Ypsolopha sp. reared from larvae collected on Adesmia spinosissima Meyen, dorsal view, abdomen removed. Scale bar: 5 mm.
Fig. 12 in Using RADseq to resolve species boundaries in a morphologically complex group of yellow-flowered shrubs (Geleznowia, Rutaceae)
Fig. 12. (Caption on next page)
Fig. 1 in Using RADseq to resolve species boundaries in a morphologically complex group of yellow-flowered shrubs (Geleznowia, Rutaceae)
Fig. 1. (Caption on next page)
Root traits reveal safety and efficiency differences in grasses and shrubs exposed to different fire regimes
<p>Roots are key components of terrestrial ecosystems, yet little is known about how root structure and function vary across a broad range of species, functional groups, and ecological gradients <i>in situ</i>.</p> <p>We assessed how woody and grass root anatomical traits vary among soil depths and different fire frequencies to better understand the water-use strategies exhibited by these two functional groups in tallgrass prairie experiencing woody encroachment. Specifically, we asked: (1) Do root anatomical traits differ with fire frequency or soil depth? (2) Do relationships between anatomical traits that confer hydraulic safety versus efficiency vary by fire frequency or soil depth? (3) Is root anatomy associated with integrative root traits (e.g., root diameter, specific root length (SRL), and root biomass)? (4) When scaled by root biomass, do root water-use traits impact the capacity for water uptake?</p> <p>We collected grass and woody roots from 10, 30, and 50 cm deep soil in areas burned every 1, 4, and 20-years. We then measured xylem conduit diameter, conduit cell wall thickness, conduit number, conduit mechanical safety (t/b), stele area, endoderm thickness, hydraulic diameter, theoretical hydraulic conductivity, and root-system theoretical hydraulic conductance.</p> <p>We observed: (1) Woody roots had high hydraulic conductance in shallow soils and greater mechanical strength in deeper soils, which may provide a competitive advantage in less frequently burned, more diverse plant communities; (2) Shallow grass roots had unique trait combinations at the anatomical and root-system levels (thinner, more numerous conduits and higher root-system hydraulic conductance compared to deeper roots) that likely allow these plants to rapidly use water but tolerate dry soils under multiple fire regimes; and (3) hydraulic safety versus efficiency tradeoffs translate between different hierarchical scales (i.e., from anatomical to integrative root traits).</p> <p>These results provide anatomical evidence to explain water-use dynamics in tallgrass prairie and also provide novel insight regarding functional strategies that may facilitate the conversion from grassland to shrubland in less frequently burned tallgrass prairie. Future work should investigate these dynamics <i>in situ</i>, as they may explain current and future patterns of woody-grass coexistence in tallgrass prairies.</p>
Supplementary material 1 from: Lucero JE, Noble T, Haas S, Westphal M, Butterfield HS, Lortie CJ (2019) The dark side of facilitation: native shrubs facilitate exotic annuals more strongly than native annuals. NeoBiota 44: 75-93. https://doi.org/10.3897/neobiota.44.33771
: Data type: multimedia
Figures 2- 3 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figures 2- 3 Sabulopteryxbotanica, adults. 1 Male paratype, Halswell Quarry (Kennedy's Bush Rd), Christchurch MC, 29 Mar 2014 (NZAC) 2 female paratype, Christchurch Botanic Gardens MC, emg. 24 Apr 2014 (NZAC).
Figures 4-6 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figures 4-6 Sabulopteryxbotanica, adult morphology. 4 Wing venation 5 male abdominal base 6 male abdomen, segments 7–8 (sternites on left).
Figures 16-18 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figures 16-18 Sabulopteryxbotanica, late mine, cocoon, and parasitoid. 16 Fully formed mine with silk spinning causing creases 17 folded leaf with cocoon 18Sympiesis sp. (Hymenoptera: Eulophidae) partially emerged from cocoon of S.botanica in leaf from herbarium sheet AK285999 (Auckland Museum).
Figure 19 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figure 19 Distribution of Teucriumparvifolium and Sabulopteryxbotanica based mainly on records from herbarium sheets in Allan Herbarium, Lincoln and Auckland Museum herbarium.
Figures 12-15 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figures 12-15 Sabulopteryxbotanica, larva, host plant, and early mine. 12 Larva, dorsal 13Teucriumparvifolium in flower, Longbush, Wairarapa (photo courtesy of J. Rolfe) 14 initial linear mine on leaf underside 15 early blotch mine.
Figure 1 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figure 1 Teucriumparvifolium. The specimen from Awahuri Reserve, Feilding, collected by AE Esler on 23 Dec 1961, on which the first mine of Sabulopteryxbotanica was detected (Auckland Museum AK362379). Photograph courtesy of Ewen Cameron, Auckland Museum herbarium: the sheet label has been enlarged in this reproduction relative to the specimen.
Figure 20 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figure 20 Bayesian consensus phylogeny reconstructed from the COI gene. Numbers above branches represent posterior probabilities. Branch lengths are drawn proportional to the estimated number of substitutions per site, following the scale bar. The tree is rooted with Anthophilafabriciana (Choreutidae).
Figures 7-11 from: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 865: 39-65. https://doi.org/10.3897/zookeys.865.34265
Figures 7-11 Sabulopteryxbotanica, adult and pupal morphology. 7 Male genital capsule 8 male phallus 9 female genitalia 10 pupal exuviae, head, ventral view 11 pupal exuviae, thorax and abdomen, dorsal view.
Fig. 3 in Frankenia fruticosa (Frankeniaceae), a new dwarf shrub from the Knersvlakte, Western Cape
Fig. 3. Distribution of Frankenia fruticosa.
the diversity of indigenous legume fodder trees and shrubs with plots on the bases of land use and agroecology in Gamo zone, Ethiopia
<p>the data was collected from Gamo zone, SNNPRS, Ethiopia. It was about the diversity of indigenous legume fodder tree and shrub with plots on the bases of land use and agroecology. the data was collected from four land uses namely farm land, homestead, grazing land and area closure in three agroe-ecology zones namely lowland, midland and highland. </p>
Diploid and haploid assemblies and annotation of monoecious shrub willow (Salix purpurea), clone ID 94003
<p>The Salicaceae are dioecious perennials that utilize different sex determination systems. There is substantial interest in understanding the impacts of hybridization, speciation, and polyploidy on sex chromosome evolution. Here, a rare monoecious <em>S. purpurea</em> genotype, 94003, was assembled. Based on sequence alignments to dioecious and monoecious genomes, a 1.15 Mb sex-linked region on Chr15W was identified as absent in monecious plants. Inheritance of this structural variation is responsible for the loss of a male-suppressing function in what would otherwise be genetic females, resulting in monoecy or lethality, if homozygous.</p>
FIGURE 5 in Perennial shrubs in Egypt: current status and updated red data list
FIGURE 5. Number of shrubs in the Egyptian flora in relation to their floristic regions.
FIGURE 7 in Perennial shrubs in Egypt: current status and updated red data list
FIGURE 7. Summary of threats to all perennial shrubs assessed in Egypt.
FIGURE 2 in Perennial shrubs in Egypt: current status and updated red data list
FIGURE 2. Grid map distribution of the recorded woody perennials in Egypt.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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