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263 results for “acacia”
Data from: Genetic connectivity and diversity in inselberg populations of Acacia woodmaniorum, a rare endemic of the Yilgarn Craton banded iron formations
Historically rare plant species with disjunct population distributions and small population sizes might be expected to show significant genetic structure and low levels of genetic diversity due to the effects of inbreeding and genetic drift. Across the globe terrestrial inselbergs are habitat for rich, often rare and endemic flora and are valuable systems for investigating evolutionary processes that shape patterns of genetic structure and levels of genetic diversity at the landscape scale. We assessed genetic structure and levels of genetic diversity across the range of the historically rare inselberg endemic Acacia woodmaniorum. Phylogeographic and genetic structure indicates that connectivity is not sufficient to produce a panmictic population across the limited geographic range of the species. However, historical levels of gene flow are sufficient to maintain a high degree of adaptive connectivity across the landscape. Genetic diversity indicates gene flow is sufficient to largely counteract any negative genetic effects of inbreeding and random genetic drift in even the most disjunct or smallest populations. Phylogeographic and genetic structure, a signal of isolation by distance, and a lack of evidence of recent genetic bottlenecks suggest long term stability of contemporary population distributions and population sizes. There is some evidence that genetic connectivity among disjunct outcrops may be facilitated by the occasional long distance dispersal of Acacia polyads carried by insect pollinators moved by prevailing winds.
Figure 3 in The Lepidoptera of Acacia domatia in Kenya, with description of two new genera and six new species
Figure 3. (A) Phthoropoea chalcomochla; (B) Endotera nodi; (C) Kenyatta iodes; (D) Hystrichophora vittana; (E) Hystrichophora bopprei; (F) Hystrichophora griseana;
Figure 1 in The Lepidoptera of Acacia domatia in Kenya, with description of two new genera and six new species
Figure 1. (A) Acacia drepanolobium showing the domatia; (B) domatium of A. drepanolobium showing "shields" protecting larvae from ants; (C) domatium of A. drepanolobium with larvae of Endotera nodi and silken tube made by Phthoropoea chalcomochla; (D) Larva of Hystrichophora vittana; (E) domatium of A. zanzibarica with frass exuded by Hystrichophora bopprei.
Figs. 1–4. 1 in First Report of Myllocerus scapularis Roelofs (Coleoptera: Curculionidae) and Rhytiphora bankii (Fabricius) (Coleoptera: Cerambycidae) on Commercial Plantings of Acacia crassicarpa (Fabaceae) in Indonesia
Figs. 1–4. 1) A leaf of Acacia crassicarpa damaged by Myllocerus scapularis adults in a commercial nursery in Sei Kebaro Sector, North Sumatra, Sumatra, Indonesia. 2–3) Damage on a young A. crassicarpa tree in a commercial stand of this plant by an adult Rhytiphora bankii in Pelalawan South Sector, Riau, Sumatra, Indonesia: 2) Overview; 3) Closeup view. 4) R. bankii adult, dorsal view.
Organelle reads from Acacia pycnantha
<p>Organelle reads from <em>Acacia pycnantha</em>, to accompany a manuscript. This manuscript assembles a mitochondrial genome (the mitome) and a chloroplast genome (the plastome). </p> <p>In this repository, there are six files of sequencing reads. These were extracted from the full <em>Acacia pycnantha</em> data set, in NCBI under BioProject PRJNA752212.</p> <p><strong>How were these reads extracted? </strong></p> <p>For full detail, see manuscript sections: Extraction and assembly of organelle-only Nanopore reads, round 1 and round 2, and Extraction of organelle-only Illumina reads, in https://www.biorxiv.org/content/10.1101/2020.12.22.423164v1</p> <p><strong> Summary:</strong></p> <p>Extraction and assembly of organelle-only Nanopore reads, round 1</p> <p>To extract the organelle-only reads from the full read sets, we used a set of known sequences from related taxa as “baits”. For the plastome, we used three coding sequences from Acacia ligulata (NC_026134.2) in FASTA nucleotide format. We chose the genes rbcL, matK and ndhF as these are all likely to be plastid-only genes and are also well conserved. The rbcL and matK genes are usually located at either end of the LSC region, and ndhF is usually in the SSC region; these are well spaced around the plastid so that long reads should be extracted with roughly even coverage. As the mitome is much larger than the plastome, we used all 38 of the coding sequences from the mitome Acacia ligulata (NC_040998.1). </p> <p>We mapped the raw Nanopore reads (~5.5 million) to the baits with minimap2 and used samtools to extract mapped reads. We then used Filtlong to keep only the longest of the extracted reads up to a coverage of X250, because assembly becomes more fragmented or not possible when coverage is too high (and preliminary tests confirmed this with our data). For the plastome, we extracted ~28,000 reads, downsampled to 901 reads, longest ~121 Kbp; for the mitome, we extracted ~14,000 reads, no downsampling as coverage did not meet cutoff (X250), longest ~105 Kbp. Extracted Nanopore reads were assembled with Flye and the assembly was polished with two rounds of Racon.</p> <p>Extraction and assembly of organelle-only Nanopore reads, round 2</p> <p>We used this first assembly as the baits file for the next round of extracting organelle reads from the original full read set. In Minimap2, we set a minimum match value to 5000, as preliminary tests showed that more leniency here resulted in too many reads extracted to assemble properly. Again we kept only the longest reads to a target coverage of X250. From the ~5.5 million raw reads, for the plastome, we extracted ~70,000 reads (approx twice as many as in round 1), downsampled to 864 reads, longest ~121,000 bp (same as round 1); for the mitome, we extracted ~14,000 reads (similar to round 1), downsampled slightly to ~12,000 reads, longest ~105 Kbp (same as round 1). As in the first round, these reads were then assembled with Flye and polished with two rounds of Racon. In testing, further rounds of Racon polishing made little difference.</p> <p><strong>These are read sets:</strong></p> <ul> <li> <p><strong>mitome_nano_extracted_long2.fq.gz</strong></p> </li> <li> <p><strong>plastome_nano_extracted_long2.fq.gz</strong></p> </li> </ul> <p> </p> <p>Extraction of organelle-only Illumina reads</p> <p>Using the Round 2 assembly as baits, we then extracted organelle-only reads from the filtered and trimmed Illumina reads (~410 million read pairs). The extracted read sets were then randomly downsampled to a coverage of X250 using Rasusa. For the plastome, this resulted in ~26 million read pairs, downsampled to ~130,000 read pairs; for the mitome, this resulted in ~23 million read pairs, downsampled to ~670,000 read pairs. </p> <p><strong>These are read sets:</strong></p> <ul> <li> <p><strong>mitome_R1_extracted_subset.fq.gz</strong></p> </li> <li> <p><strong>mitome_R2_extracted_subset.fq.gz</strong></p> </li> <li> <p><strong>plastome_R1_extracted_subset.fq.gz</strong></p> </li> <li> <p><strong>plastome_R2_extracted_subset.fq.gz</strong></p> </li> </ul> <p> </p>
FIGURES 16–23 in A new Australian species of invasive psyllid, Acizzia convector Burckhardt & Taylor, sp. nov. (Psylloidea: Psyllidae) associated with Acacia auriculiformis and A. mangium (Fabaceae)
FIGURES 16–23. Acizzia convector Burckhardt & Taylor, sp. nov., terminalia; 16, male terminalia, in profile; 17, posterior lobe of male proctiger; 18, paramere, inner face in profile; 19, distal portion of aedeagus, in profile; 20, female terminalia, in profile; 21, detail of circumanal ring; 22, hooked seta; 23, valvulae dorsalis and ventralis.
FIGURES 1–4. 1–3 in A new Australian species of invasive psyllid, Acizzia convector Burckhardt & Taylor, sp. nov. (Psylloidea: Psyllidae) associated with Acacia auriculiformis and A. mangium (Fabaceae)
FIGURES 1–4. 1–3, Acizzia convector Burckhardt & Taylor, sp. nov. (photographs by Lyle Buss, University of Florida); 1, male; 2, female; 3, immature.—4, Monoculture of Acacia auriculiformis trees 6 m high in Florida. This field was bare ground three years prior to taking this photograph (photograph by Scott D. Krueger, Florida Department of Agriculture and Consumer Services, Division of Plant Industry).
FIGURES 5–15 in A new Australian species of invasive psyllid, Acizzia convector Burckhardt & Taylor, sp. nov. (Psylloidea: Psyllidae) associated with Acacia auriculiformis and A. mangium (Fabaceae)
FIGURES 5–15. Acizzia convector Burckhardt & Taylor, sp. nov., adults; 5–8, habitus; 5, 6, lateral view; 7, 8, dorsal view; 5, 7, 12, 14, male; 6, 8, 13, female; 9, head, dorsal view; 10, vertex, right half; 11, metatibia, base with genual spine; 12–14, fore wing; 12, 13, wing pattern; 14 surface spinules; 15, details of surface spinules in apical third of cell r2.
Data from: Genetic connectivity and diversity in inselberg populations of Acacia woodmaniorum, a rare endemic of the Yilgarn Craton banded iron formations
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Data from: A biogeographical regionalisation of Australian Acacia species
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Data from: Varying levels of clonality and ploidy create barriers to gene flow and challenges for conservation of an Australian arid-zone ecosystem engineer, Acacia loderi
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Data from: Contrasting influences of geographic range and distribution of populations on patterns of genetic diversity in two sympatric Pilbara Acacias
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Data from: Importance of soil legacy effects and successful mutualistic interactions during Australian acacia invasions in nutrient poor environments
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Data from: Impacts of worker density in colony-level aggression, expansion, and survival of the acacia-ant Crematogaster mimosae
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Data from: Applying landscape genomic tools to forest management and restoration of Hawaiian koa (Acacia koa) in a changing environment
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Data from: Evidence for enemy release and increased seed production and size for two invasive Australian acacias
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Data from: Polygyny does not explain the superior competitive ability of dominant ant associates in the African ant-plant, Acacia (Vachellia) drepanolobium
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Data from: Dietary specialization in mutualistic acacia-ants affects relative abundance but not identity of host-associated bacteria
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Data from: Evolutionary history shapes patterns of mutualistic benefit in Acacia-rhizobial interactions
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Data from: Fire after a mast year triggers mass recruitment of slender mulga (Acacia aptaneura), a desert shrub with heat-stimulated germination
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