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FIGURES 26–28 in Taxonomic revision of Scoparia Haworth, 1811 (Lepidoptera: Crambidae: Scopariinae) from China
FIGURES 26–28. Female genitalia of Scoparia spp.: 26, S. jiuzhaiensis sp. n., paratype, genitalia slide no. LWC08055; 27, S. uncinata sp. n., paratype, genitalia slide no. LWC06312; 28, S. brevituba sp. n., paratype, genitalia slide no. LWC07486.
FIGURES 1–4. Scoparia sinensis Leraut, 1986 in Taxonomic revision of Scoparia Haworth, 1811 (Lepidoptera: Crambidae: Scopariinae) from China
FIGURES 1–4. Scoparia sinensis Leraut, 1986: 1, adult; 2, tympanal organ, slide no. LWC08048; 3, male genitalia (a, male genitalia capsule; b, phallus; c, cornuti), genitalia slide no. LWC06251; 4, female genitalia, genitalia slide no. LWC08048.
FIGURE. Serpentine pine forests (Pinus pinaster) accompanied by Erica scoparia and Quercus coccifera, climax vegetation in the Bermejense sector. (Photo authors). in Vascular flora of the Sierra de las Nieves National Park and its surroundings (Andalusia, Spain)
FIGURE. Serpentine pine forests (Pinus pinaster) accompanied by Erica scoparia and Quercus coccifera, climax vegetation in the Bermejense sector. (Photo authors).
FIGURES 1–6. Scoparia juldusellus. 1 in Scoparia juldusellus (Caradja, 1916), a little-known snout moth species new to the fauna of Kyrgyzstan (Lepidoptera: Crambidae: Scopariinae)
FIGURES 1–6. Scoparia juldusellus. 1—male, Kara-Buura River valley; 2—male, Dolon Pass; 3—male genitalia, Kara-Buura valley, ventral view (aedeagus removed); 4—the same, aedeagus; 5, 6—habitats in Kyrgyzstan (5—Dolon Pass, Inner Tien-Shan; 6—Kara-Buura River valley, West Tien-Shan).
Data from: Chromosome scale genome assemblies and annotations for Poales species Carex cristatella, Carex scoparia, Juncus effusus and Juncus inflexus
<p>The majority of sequenced genomes in the Monocots are from species belonging to the Poaceae, which includes many commercially important crops. Here, we expand the number of sequenced genomes from the Monocots to include the genomes of four related Cyperids: <em>Carex cristatella</em> and <em>Carex scoparia</em> from Cyperaceae and <em>Juncus effusus</em> and <em>Juncus inflexus</em> from Juncaceae. The high-quality, chromosome-scale genome sequences from these four Cyperids were assembled by combining whole-genome shotgun sequencing of Nanopore long reads, Illumina short reads, and Hi-C sequencing data. Some members of the Cyperaceae and Juncaceae are known to possess holocentric chromosomes. We examined the repeat landscapes in our sequenced genomes to search for potential repeats associated with centromeres. Several large satellite repeat families, comprising 3.2% to 9.5% of our sequenced genomes, showed dispersed distribution of large repeat clusters across all <em>Carex</em> chromosomes, with few instances of these repeats clustering in the same chromosomal regions. In contrast, most large <em>Juncus</em> satellite repeats were clustered in a single location on each chromosome, with sporadic instances of large satellite repeats throughout the Juncus genomes. Recognizable transposable elements account for about 20% of the assemblies, with the <em>Carex</em> genomes containing more DNA transposons than retrotransposons while the converse is true for the <em>Juncus</em> genomes. These genome sequences and annotations will facilitate better comparative analysis within monocots.</p>
FIGURE 68. Daviesia scoparia. A. Flowering branchlet. B. Inflorescence. C. Pod. A from Kuchel 1717 in A monograph of Daviesia (Mirbelieae, Faboideae, Fabaceae)
FIGURE 68. Daviesia scoparia. A. Flowering branchlet. B. Inflorescence. C. Pod. A from Kuchel 1717; B from Crisp 6142 (type); C from Crisp 5196. Drawn by B.J. Osborne. Adapted from Crisp (1995) with permission from CSIRO Publishing.
Figure 10 in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 10. Map of China showing the topography and localities where Scoparia spp. are recorded, the coloured dots indicate the recorded localities and species numbers.
Figure 6. A–C in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 6. A–C, male genitalia of of Scoparia spp. A, Scoparia globosa Li sp. nov., holotype, prep. gen. no. LW12007; B–C, Scoparia annulata Li sp. nov.; B, holotype, prep. gen. no. LW12014; C, paratype, prep. gen. no. LW12026.
Figure 5. A–B in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 5. A–B, male genitalia of of Scoparia metaleucalis Hampson, 1907. A, prep. gen. no. LW12074; B, prep. gen. no. LW12088.
Figure 2. Minimum-evolution tree deduced from cytochrome c oxidase subunit I in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 2. Minimum-evolution tree deduced from cytochrome c oxidase subunit I (COI) gene sequences. Sequences were corrected with the Kimura two-parameter substitution model. Codon positions included were 1st + 2nd + 3rd + noncoding. Values represented at the nodes of branches are bootstrap values (1000 replicates).
Figure 9. A–C in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 9. A–C, female genitalia of Scoparia spp. A, Scoparia brevituba Li, Li & Nuss, 2010, prep. gen. no. LW12032; B, Scoparia globosa Li sp. nov., paratype, prep. gen. no. LW12025; C, Scoparia annulata Li sp. nov., paratype, prep. gen. no. LW12022.
Figure 4. A–C in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 4. A–C, male genitalia of Scoparia spp. A, Scoparia simplicissima Li sp. nov., holotype, prep. gen. no. LW12094; B, Scoparia tribulosa Li sp. nov., holotype, prep. gen. no. LW12027; C, Scoparia longispina Li sp. nov., holotype, prep. gen. no. LW12044.
Figure 8. A–C in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 8. A–C, female genitalia of Scoparia spp. A–B, Scoparia metaleucalis Hampson, 1907; A, prep. gen. no. LW13044; B, prep. gen. no. LW12049; C, Scoparia jiuzhaiensis Li, Li & Nuss, 2010, prep. gen. no. LW12036.
Figure 1. Neighbour-joining tree deduced from the cytochrome c oxidase subunit I in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 1. Neighbour-joining tree deduced from the cytochrome c oxidase subunit I (COI) gene sequences using MEGA 5. Sequences were corrected with the Kimura two-parameter substitution model. Codon positions included were 1st + 2nd + 3rd + noncoding. Values represented at the nodes of branches are bootstrap values (1000 replicates).
Figure 7. A–C in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 7. A–C, female genitalia of Scoparia spp. A–B, Scoparia tribulosa Li sp. nov., paratypes; A, prep. gen. no. LW12016; B, prep. gen. no. LW13020; C, Scoparia gibbosa Li sp. nov., holotype, prep. gen. no. LW12009.
Figure 3. A–I in DNA barcoding and morphology reveal exceptional species diversity of Scoparia (Lepidoptera: Crambidae) from the Hailuogou Glacier area, China
Figure 3. A–I, adults of Scoparia spp. A, Scoparia simplicissima Li sp. nov., male, paratype; B, Scoparia tribulosa Li sp. nov., female, paratype; C, Scoparia longispina Li sp. nov., male, paratype; D, Scoparia gibbosa Li sp. nov., female, paratype; E, Scoparia metaleucalis Hampson, 1907, female; F, Scoparia jiuzhaiensis Li, Li & Nuss, 2010, female; G, Scoparia brevituba Li, Li & Nuss, 2010, female; H, Scoparia globosa Li sp. nov., female, paratype; I, Scoparia annulata Li sp. nov., male, paratype. Scale bars: 5 mm.
FIGURE 3 in Additions to Peroneutypa (Diatrypaceae, Xylariales): Introducing P. nayariophyti sp. nov. and new host associations of P. scoparia from northern Thailand
FIGURE 3. Peroneutypa nayariophyti (MFLU 23-0077, holotype). a Appearance of ascostromata on Nayariophyton zizyphifolium woody litter. b Upper view of the cross-section of ascostromata. c Cross section of ascostromata (arrowed). d, e Appearance of ascomata with a long neck on the substrate. f Peridium. g Paraphyses. h–m Asci. n–r Ascospores. s Germinated spore. t, u Culture characteristics on PDA from front and reverse. Scale bars: a = 1 mm, b–d = 500 μm, e = 200 μm, f = 50 μm, g–m, r, s = 10 μm, n–q = 5 μm.
FIGURE 1. Maximum likelihood tree from combined ITS and tub2 in Additions to Peroneutypa (Diatrypaceae, Xylariales): Introducing P. nayariophyti sp. nov. and new host associations of P. scoparia from northern Thailand
FIGURE 1. Maximum likelihood tree from combined ITS and tub2 sequence data. Bootstrap support values ≥ 60% and Bayesian posterior probabilities ≥ 0.90 are indicated at the branches. The tree is rooted with Xylaria polysporicola (FCATAS848) and X. hypoxylon (CBS 122620). The taxa originating from this study are shown in blue. Type species are in bold.
FIGURE 4 in Additions to Peroneutypa (Diatrypaceae, Xylariales): Introducing P. nayariophyti sp. nov. and new host associations of P. scoparia from northern Thailand
FIGURE 4. Peroneutypa scoparia (MFLU 23-0079, new host record). a Appearance of ascomata on Dalbergia cana woody litter. b, c Close up of ascomata on host substrate. d Vertical section through ascomata. e Cross-section of peridium. f Ostiol canal. g Paraphyses. h–m Asci. n–r Ascospores. s Germinated spore. t, u Culture characteristics on PDA from the front and reverse. Scale bars: a = 1 mm, b, c = 500 μm, d = 200 μm, g = 50 μm, e, f, h–j, l, s = 20 μm, k, m, r = 10 μm, n–q = 5 μm.
Data from: Speciation, population structure, and demographic history of the Mojave Fringe-toed Lizard (Uma scoparia), a species of conservation concern
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