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2,885 results for “Transfers”
FIGURE 22–26 in Revision and transfer of Neotropical genera of the tribe Morimopsini Lacordaire, 1869 (Coleoptera: Cerambycidae): new species, redescription, taxonomic notes, and species key
FIGURE 22–26. Polytuberotum boteroi sp. nov., holotype male: 22, dorsal habitus; 23, ventral habitus; 24, lateral habitus; 25, head, frontal view; 26, detail pronotum and elytral tubercles, dorsal view.
FIGURE 2–6 in Revision and transfer of Neotropical genera of the tribe Morimopsini Lacordaire, 1869 (Coleoptera: Cerambycidae): new species, redescription, taxonomic notes, and species key
FIGURE 2–6. Holotype male, Tuberolamia andicola Breuning, 1940; 2, dorsal habitus; 3, lateral habitus; 4, labels; 5, ventral habitus; 6, head, frontal view.
FIGURE 17–21 in Revision and transfer of Neotropical genera of the tribe Morimopsini Lacordaire, 1869 (Coleoptera: Cerambycidae): new species, redescription, taxonomic notes, and species key
FIGURE 17–21. Tuberolamia santossilvai sp. nov., holotype male: 17, dorsal habitus; 18, ventral habitus; 19, lateral habitus; 20, head, frontal view; 21, detail elytral tubercles, lateral view.
FIGURE 1 in Revision and transfer of Neotropical genera of the tribe Morimopsini Lacordaire, 1869 (Coleoptera: Cerambycidae): new species, redescription, taxonomic notes, and species key
FIGURE 1. Distribution map of Morimopsini species in the Neotropics. A: Peru; B: Known distribution of Tuberolamia andicola (red star), T. grilloides (green star), T. santossilvai (black star), Polytuberotum metachroma (orange asterisk), and P. boteroi (blue asterisk).
FIGURE 12–16 in Revision and transfer of Neotropical genera of the tribe Morimopsini Lacordaire, 1869 (Coleoptera: Cerambycidae): new species, redescription, taxonomic notes, and species key
FIGURE 12–16. Holotype male, Tuberolamia andicola Breuning, 1940: 12, dorsal habitus; 13, ventral habitus; 14, lateral habitus; 15, head, frontal view; 16, labels.
Many-Body Models for Chirality-Induced Spin Selectivity in Electron Transfer. Open data set
<p>Data supporting the original figures 1, 2, 3 and 4 of the related publication.</p>
China's Greener Production Reduces East-to-West Pollution Transfers and Alleviates Environmental-Economic Inequalities
<p>The data contains 1. Pro-andCon-base_APE_Value added (the production- and consumption-based APE and value added in 2007, 2012, 2017, and the change); 2. f_d (the production- and consumption-based emission intensity (<em>f</em>) and value added intensity (<em>d</em>) in 2007, 2012, 2017); 3. REI_REIC (the REI index in 2007 and 2017, and REIC index); 4. ape_flow2007 (the APE flows in 2007); 5. ape_flow2012 (the APE flows in 2012); 6. ape_flow2017 (the APE flows in 2017); 7. ape_flowchange (the change of the APE flows from 2007 to 2017); 8. va_flow2007 (the value added flows in 2007); 9. va_flow2012 (the value added flows in 2012); 10. va_flow2017 (the value added flows in 2017); 11. va_flowchange (the change of the value added flows from 2007 to 2017);</p>
Reproduction package for the paper "BH-BH mergers with & without EM counterpart: A model for stable tertiary mass transfer in hierarchical triple systems"
<p>This is a reproduction package for the paper "BH-BH mergers with & without EM counterpart: A model for stable tertiary mass transfer in hierarchical triple systems" by Kummer et al. (2024). It aims to provide the most important data products and reproduce the Figures of the paper.</p> <p> </p>
Data from: Grafting or pruning in the animal tree: lateral gene transfer and gene loss?
Background: Lateral gene transfer (LGT), also known as horizontal gene transfer, into multicellular eukaryotes with differentiated tissues, particularly gonads, continues to be met with skepticism by many prominent evolutionary and genomic biologists. A detailed examination of 26 animal genomes identified putative LGTs in invertebrate and vertebrate genomes, concluding that there are fewer predicted LGTs in vertebrates/chordates than invertebrates, but there is still evidence of LGT into chordates, including humans. More recently, a reanalysis of a subset of these putative LGTs into vertebrates concluded that there is not horizontal gene transfer in the human genome. One of the genes in dispute is an N-acyl-aromatic-L-amino acid amidohydrolase (ENSG00000132744), which encodes ACY3. This gene was initially identified as a putative bacteria-chordate LGT but was later debunked as it has a significant BLAST match to a more recently deposited genome of Saccoglossus kowalevskii, a flatworm, Metazoan, and hemichordate. Results: Using BLAST searches, HMM searches, and phylogenetics to assess the evidence for LGT, gene loss, and rate variation in ACY3/ASPA homologues, the most parsimonious explanation for the distribution of ACY3/ASPA genes in eukaryotes involves both gene loss and bacteria-animal LGT, albeit LGT that occurred hundreds of millions of years ago prior to the divergence of gnathostomes. Conclusions: ACY3/ASPA is most likely a bacteria-animal LGT. LGTs at these time scales in the ancestors of humans are not unexpected given the many known, well-characterized, and adaptive LGTs from bacteria to insects and nematodes.
FIGURES 1–4 in A review of the type material of the Southern African genus Stenobasipteron Lichtwardt, 1910 (Diptera: Nemestrinidae), with transfer of two species to Prosoeca Schiner, 1867
FIGURES 1–4. Wings of Stenobasipteron and Prosoeca. 1–3. Stenobasipteron. 1. S. arnoldi, female holotype. 2. S. gracile, male syntype. 3. S. wiedemanni, male syntype (bulla at base of first longitudinal vein arrowed). 4. Prosoeca umbrosa, male syntype.
FIGURE 1 in A 150 year-old mystery solved: Transfer of the rheophytic endemic liverwort Myriocolea irrorata to Colura
FIGURE 1. Single most likely tree (ln= -9,559.44384) derived from a cp DNA rbcL-trnL-F – nrITS dataset. ML bootstrap values (bold) and MP bootstrap values (not bold) are indicated at branches. Two accessions of Myriocolea irrorata are nested in a robust subclade of Colura, and are placed sister to the Colura-generitype, C. calyptrifolia.
Multiscale modelling of flow, heat transfer and transformation during thermal treatment of starch suspensions
<p>Multiscale modelling of flow, heat transfer and transformation during thermal treatment of starch suspensions</p>
Photo-triggered hydrogen atom transfer from an iridium hydride complex to unactivated olefins
<p>Data underlying the figures in the publication “Photo-triggered hydrogen atom transfer from an iridium hydride complex to unactivated olefins”, published in <strong><em>Chem. Sci.</em></strong>,<strong> 2020, </strong><strong>11</strong><strong>,</strong> 8582-8594. <a href="https://pubs.rsc.org/en/content/articlelanding/2020/sc/d0sc01820a#!divAbstract">https://pubs.rsc.org/en/content/articlelanding/2020/sc/d0sc01820a#!divAbstract</a></p> <p>Table of contents:</p> <p><strong>1. Figure 7</strong>; Excel file containing all raw data of <em>Figure 7</em>.</p> <p>Transient absorption spectrum of a solutions containing <strong>[Cp*Ir(phen)(H)](PF<sub>6</sub>)</strong> (0.5 mM) measured at different conditions (<em>Figure 7a</em> and <em>7b</em>); and absorption spectra of <strong>[Cp*Ir(phen)]<sup>0</sup></strong> (<em>Figure 7c</em>) and of TAA-OMe˙<sup>+</sup> (<em>Figure 7d</em>).</p> <p>Detailed conditions can be found in the publication.</p>
How Can Giant Plasma Membrane Vesicles Serve as a Cellular Model for Controlled Transfer of Nanoparticles?
<p>Data underlying the figures in the publication “How Can Giant Plasma Membrane Vesicles Serve as a Cellular Model for Controlled Transfer of Nanoparticles?”, published in <em>Biomacromolecules</em>, <strong>2021</strong>, 22, 1, 106–115.</p> <p><a href="https://pubs.acs.org/doi/10.1021/acs.biomac.0c00624">https://pubs.acs.org/doi/10.1021/acs.biomac.0c00624</a></p> <p>Table of contents:</p> <p><strong>1. Figure 1</strong>; Zip file containing the data for <em>Figure 1</em>.</p> <p><strong>2. Figure 2</strong>; Zip file containing the TEM micrographs for <em>Figure 2</em>.</p> <p><strong>3. Figure 4</strong>; Zip file containing numerical data of the flow cytometry measurements and analysis for <em>Figure 4</em>.</p> <p><strong>4. Figure 5</strong>; Zip file containing the data for <em>Figure 5</em>.</p> <p><strong>5. Figure 6,7</strong>; Zip file containing numerical data for <em>Figures 6 </em>and <em>7</em>.</p>
FIGURE 1 in Notes on Early Land Plants Today. 46. Transfer of Vitalianthus urubuensis (Marchantiophyta, Lejeuneaceae) to Cheilolejeunea
FIGURE 1. Cheilolejeunea urubuensis (Zartman & I.L.Ackerman) R.L.Zhu & Y.M.Wei. A. Portion of plant with perianth. B. Portion of plant, showing underleaves. C. Portion of plant, ventral view. D. Leaf, ventral view. E, F. Leaf lobule, showing a hyaline papilla (arrow). A from Laura V. Campos 713 (HSNU); B, F from Laura V. Campos 712 (HSNU); C-E from C.E. Zartman 2626 (isotype, DUKE).
FIGURES 51–58 in Transfer of Fragilaria atomus Hust. to the genus Stauroforma (Bacillariophyta) based on observation of type and newly collected material
FIGURES 51–58. SEM: Stauroforma atomus comb. nov. BRM E2963 (lectotype). Figs 51–56. External view of valve showing headpole (white arrow) and foot-pole (black arrow). Fig. 56. Detail of curved striae with different sizes at head-pole (arrow). Fig. 57. Detail of foot-pole with the poroids of the apical pore field (arrow) and areolae containing a slightly branched structure. Fig. 58. Internal view of valve showing two poroids at foot-pole (arrow). Scale bars = 1.5 µm (Figs 51, 53–54), 1 µm (Figs 52, 55–56, 58), 500 nm (Fig. 57).
FIGURE 65 in Transfer of Fragilaria atomus Hust. to the genus Stauroforma (Bacillariophyta) based on observation of type and newly collected material
FIGURE 65. Global distribution of Stauroforma atomus as recored in Table 2 (grey star = type locality; black star = population from Brazil; black dots = all other records).
FIGURES 59–64 in Transfer of Fragilaria atomus Hust. to the genus Stauroforma (Bacillariophyta) based on observation of type and newly collected material
FIGURES 59–64. SEM: Stauroforma atomus comb. nov. from Brazil. Figs 59–60, 63–64. External view of valve showing head-pole (white arrow) and foot-pole (black arrow). Fig. 61. Detail of foot-pole with the poroids of the apical pore field (arrow) and areolae containing a slightly branched structure. Fig. 62. Detail of curved striae with different sizes at head-pole (arrow). Scale bars = 1 µm (Figs 59–60, 63–64), 0.5 µm (Figs 61–62).
FIGURES 1–50 in Transfer of Fragilaria atomus Hust. to the genus Stauroforma (Bacillariophyta) based on observation of type and newly collected material
FIGURES 1–50. LM: Stauroforma atomus comb. nov. Fig. 1. Iconotype reproduced from Hustedt (1931, fig. 672B) illustrating specimens in valve view and a pair of frustules in girdle view. Figs 2–31. Specimens BRM E2963 (lectotype). Figs 28–31. Girdle view. Figs 32–50. Specimens from Brazil. Scale bar = 5 µm.
FIGURE 2 in Towards a monophyletic classification of Lejeuneaceae II: subtribes Pycnolejeuneinae and Xylolejeuneinae subtr. nov., transfer of Otolejeunea to Lepidolejeuninae, and generic refinements
FIGURE 2. Majority rule consensus tree of trees recovered in stationary phase of Bayesian search. Support (≥ 0.95) from Bayesian searches is indicated at branches.
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Annotated Behaviour and Observability Dataset (ABODe)
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