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FIGURE 6 in Redescription of two species and proposal of a new synonym in the genus Mycotretus Lacordaire, 1842 (Coleoptera: Erotylidae: Tritomini)
FIGURE 6. (A–D) male terminalia of a paratype of Mycotretus trifasciatus Guérin, 1956 from Cerro Azul (PR, Brazil), (A) penis (pen), flagellum (fla), apophyses (apo), with arrow showing the median sinuosity of flagellum; (B) detail of the sinuosity, with arrow showing a sclerotization not observed in M. chilensis; (C) tegmen, with arrow showing parameres; (D) tergite IX and segment X, with arrow showing anteroventral edge of segment IX. (E) female genitalia of a paratype of M. trifasciatus from Rio Vermelho (SC, Brazil), with arrows showing the gonostyli; (F) female genitalia of a M. trifasciatus from Obidos (PA, Brazil), with red arrows showing gonocoxites; (G) female genitalia of a M. trifasciatus from Viçosa (MG, Brazil), with black arrow showing the spermatheca and red arrow showing an expanded portion of the bursa copulatrix; (H) spermatheca of a paratype of M. trifasciatus from Rio Vermelho; (I) sternite VIII with a median strut (arrow) of a paratype of M. trifasciatus from Rio Vermelho. Scale bars: A–G and I = 0.5 mm, H = 0.1 mm.
FIGURE 2. Friesenhaus, Kirchenstrasse 1 in Heinrich Friese (1860-1948): Names proposed and notes on a pioneer melittologist (Hymenoptera, Anthophila)
FIGURE 2. Friesenhaus, Kirchenstrasse 1, Schwerin, Germany, where Friese conducted much of his research. Original post-card from Friese (dated March 16th, 1929).
FIGURE 1 in Heinrich Friese (1860-1948): Names proposed and notes on a pioneer melittologist (Hymenoptera, Anthophila)
FIGURE 1. Portrait of Heinrich Friese (1860–1948). From Image Archive Deutsches Entomologisches Institut, Müncheberg.
FIGURES 3–10 in Heinrich Friese (1860-1948): Names proposed and notes on a pioneer melittologist (Hymenoptera, Anthophila)
FIGURES 3–10. Examples of labels used by Friese. 3. Centris versicolor rufiventris. Syntype (ZMHB). Red Type label suggest a type; locality and specimen correspond to original description. 4. Epicharis rustica var. flava. Syntype (subsequently designated lectotype) (ZMHB). No type label from Friese, but locality, collection date, and specimen correspond with the original publication. Determination label indicates that this is a new taxon described by Friese (variously handwritten "n.var.", "n.sp.", or just "n" on other specimens). 5. Trigona keyensis. Probable syntype (AMNH). No type label on this specimen, but locality, collection date, and specimen correspond with the original publication. Determination label only indicates that Friese is the author and determiner of the species, but not that this is a new taxon. 6. Trigona flaviventris. Not a type (AMNH). Orange "Typus" label suggest a type, but specimen collected after the description of the species. 7. Megacilissa tomentosa. Syntype (ZMHB). Early orange Type label. 8. Callosphecodes ralunensis. Holotype (ZMHB). Alternative red framed Type label. Additional label indicate that this specimen was part of Friese's personal collection. 9. Trigona mellipes. Probable syntype (ZMHB). No type label on this specimen, but locality, collection date, and specimen corresponds with the original publication. Determination label only indicates that Friese is the author and determiner of the species, but not that this is a new taxon. Additional label indicate that this specimen was part of Friese's personal collection and is now deposited in ZMHB. 10. Trigona handlirschi. Probable holotype (ZMHB). Orange Typus label. T. handlirschi was described based on a single worker from "Brasilia" (here =Amazonas, Brasil, 1897), but determination label is from 909 (=1909). As this was the only specimen of this taxa encountered and because it is from the type locality and was colleted before the publication of the species, it is presumed the holotype, although the determination label does not provide evidence for this. We have seen other cases were putative types were labeled with determination labels dating after the publication of the taxa, and it is not unlikely that Friese would add these labels at later date.
FIG. 2. G in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 2. G-banded karyotype of a female N. guineensis, 2n = 26. Bold numbers for chromosomal arms indicate homology validated with painting probes from Myotis (MMY) or tree shrew (TBE30)
FIG. 6. C in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 6. C-banded metaphase spreads of (A) P. brunnea, (B) N. happoldorum, and (C) N. schlieffenii. X and Y chromosomes and heterochromatic segments of interest are indicated, numbers refer to MMY homologies. In (B), arrows point to those heterochromatic segments which showed differences between the homologs and arrowheads point to C-positive segments on pairs NHA11 and NHA13. For further explanation see main text
FIG. 5 in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 5. Rearranged bi-armed pair 3/4 of P. brunnea depicted from left to right after G-banding, C-banding, FISH with E. macaco painting probe EMA8 and T. belangeri probe TBE6. The extant centromere is indicated by a dash, the ancestral centromere position by an asterisk. In the basic karyotype, EMA8 homologous sequences were located in the proximal region of the MMY3 homologous chromosomal arms, whereas here they are found in the long arm of P. brunnea chromosome 3/4 (TBE6, homologous to parts of MMY4, was used to delimit the proximal and distal regions of the MMY4 homologous segment in P. brunnea chromosome 3/4)
FIG. 1. G in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 1. G-banded karyotype of a male L. kirinyaga, 2n = 32. Chromosomal arms are numbered according to the scheme of Bickham (1979) for Myotis species. The nucleolus organizer region (NOR) is indicated by an arrowhead
FIG. 11. G in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 11. G-banded karyotype of a female N. schlieffenii, 2n = 34. Homology to MMY validated with painting probes from MMY, Tree shrew or black lemur is indicated by bold numbers. The remaining pairs were identified by G-band comparison with other vespertilionid species
FIG. 8. The G in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 8. The G-banded karyotype of a male N. happoldorum with 2n = 24 chromosomes and their homology to M. myotis (MMY). Bold numbers indicate homology validated with FISH applying painting probes from MMY
FIG. 9 in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 9. Heteromorphic condition of the fusion products of MMY18 and NOR-bearing MMY15 homologous chromosomal arms in N. happoldorum chromosome NHA8 shown after different staining procedures and FISH from left to right: h — homogeneous Giemsa staining, G — G-banding, Ag — AgNOR staining, C — C-banding, FISH with MMY18 and MMY15 painting probes. Both homologs differ concerning the position of the centromeres, which are highlighted by dashes. The left chromosome of each pair displays the result of a centric fusion between MMY15 and MMY18 homologous chromosomal arms. On the right chromosome of each pair, the centromere is located within the MMY18 homologous arm, transforming the morphology from submetacentric to subtelocentric. Note that the NORs are positioned at the SC of the long arm, as indicated by arrowheads
FIG. 7 in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 7. Examples of G-banded X chromosomes: The banding patterns of the X chromosomes from L. kirinyaga (LKI) and N. schlieffeni (NSC) were similar to that of state II of the basic vespertilionid karyotype. The N. guineensis (NGU) X was the product of an X-autosome translocation and the X chromosomes from P. brunnea (PBR) and N. happoldorum (NHA) showed unique derived G-banding patterns
FIG. 4. G in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 4. G-banded karyotype of a male P. brunnea, 2n = 36. At the X, a horizontal line indicates the position of the centromere in the X chromosome of the basic karyotype, state II. Asterisks indicate interstitial heterochromatic segments
FIG. 3. X in Karyotype comparison of five African Vespertilionini species with comments on phylogenetic relationships and proposal of a new subtribe
FIG. 3. X-autosome translocation in N. guineensis: The X chromosomes are shown after different staining procedures and FISH (G — G-banding, C — C-banding, R — replication banding procedure). Note the dark stained, early replicating distal part of the short arm in both X chromosomes, the early replicating (left homolog of the pair) and the late replicating (XL, right) long arms of the X chromosomes. FISH with the MMY X painting probe resulted in signals on the long arm of the N. guineensis X chromosome. FISH with a painting probe containing homologous sequences to Myotis chromosome 25 revealed signals on the short arm of the X
COWORKER SUPPORT AS MODERATOR ON THE RELATIONSHIP BETWEEN HRM PRACTICES ANDORGANIZATIONAL COMMITMENT: A PROPOSED FRAMEWORK.
<p>Several factors have been proposed to have influence over organizational commitment; among some <br>of those prominent factors are human resource management practices. However, among the <br>prominent studies on the said relationship; the reported findings are inconsistent. Therefore, it is<br>proposed to incorporate a moderating variable to further explain this relationship. The current study <br>proposed coworker support as moderator on the relationship between HRM practices and<br>organizational commitment.</p>
Supplementary material 1 from: Koureas D, Livermore L, Addink W, Alonso E, Alonso JM, Casino A, Dusoulier F, Ferreira V, Grieb J, Groom Q, Islam S, Kõljalg U, Lymer G, Marhold K, Paleco C, Pijls S, Scory S, Scott B, Weiland C, Worley K (2024) DiSSCo Transition Abridged Grant Proposal. Research Ideas and Outcomes 10: e118241. https://doi.org/10.3897/rio.10.e118241
Letter of Intent for Collaboration: Development of a Global Partnership on Persistent Identification of Digital Extended Specimens & other Natural Science Collections Data Entities
Supplementary material for the paper "A bibliometric investigation on didactic proposals in interpreter training (2001-2020)"
<p>Supplementary material for the article entitled "A bibliometric investigation on didactic proposals in interpreter training (2001-2020)". It includes a readme file with instructions. VOSviewer is required to view the data (https://www.vosviewer.com). </p>
Supplemental package of a study on Microservices versus Monoliths: Identifying Challenges and Proposing Practical Recommendations
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Table A.3: New stellar multiple systems proposed
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FIGURE 8 in Contribution to the knowledge of Carabidae in Iran with the descriptions of five new taxa, proposing of four synonyms and providing of nine new records (Insecta: Coleoptera)
FIGURE 8. Porotachys ottomanus ottomanus habitus, Suq cave, scale: 2 mm. FIGURE 9. Tachyura (Tachyura) shahinei habitus, 13 km SSE Nikshahr riv., scale: 2 mm. FIGURE 10. Tachyura (Tachyura) conspicua habitus, Kuh-e Geno, scale: 2 mm. FIGURE 11. Polyderis algiricus habitus, 10 km W Naghan, scale: 1 mm. FIGURE 12. Polyderis impressipennis habitus, Minab, scale: 1 mm.
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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.