1,721,608 research outputs found
Mysteria darwini
2. Mysteria darwini (Lameere, 1902) Type locality— Brazil. (SMNS). Distribution— Brazil (Santa Catarina, Rio Grande do Sul). Anoploderma (Mysteria) Darwini Lameere, 1902b: 210; Melzer, 1919: 189. Mysteria darwini; Lane, 1937: 218; Prosen, 1960: 91 (distr.); Dias, 1988: 142, figs. 1, 7, 17, 33, 47, 70, 71, 77, 81; 2004: 141, 8 figs.Published as part of MONNÉ, MIGUEL A., 2006, Catalogue of the Cerambycidae (Coleoptera) of the Neotropical Region. Part III. Subfamilies Parandrinae, Prioninae, Anoplodermatinae, Aseminae Spondylidinae, Lepturinae, Oxypeltinae, and addenda to the Cerambycinae and Lamiinae,, pp. 1-244 in Zootaxa 1212 (1) on page 106, DOI: 10.11646/zootaxa.1212.1.1, http://zenodo.org/record/506497
Dichotomius (Cephagonus) darwini Nunes
4.2.: Dichotomius (Cephagonus) darwini Nunes & Vaz-de-Mello 2016 (Figure 41 (b)) Dichotomius (s.) darwini ı Nunes & Vaz-de-Mello 2016ı p. 82 (description) Diagnosis. In the groupı D. darwini is one of the five recognised brachypterous species and is separated from them by the wrinkling/striation on the cephalic carina. Distribution. Parque Nacional de Eması municipality of Mineirosı state of Goiásı Brazil (Figure 42).Published as part of Nunes, Rafael V. & Vaz-de-Mello, Fernando Z., 2019, Taxonomic revision of Dichotomius (Cephagonus) Luederwaldt 1929 and the taxonomic status of remaining Dichotomius Hope 1838 subgenera (Coleoptera: Scarabaeidae: Scarabaeinae: Dichotomiini), pp. 2231-2351 in Journal of Natural History 53 (37) on page 2329, DOI: 10.1080/00222933.2019.1692088, http://zenodo.org/record/366551
Polylobus darwini Bernhauer 1835
Polylobus darwini Bernhauer, 1835 Polylobus darwini Bernhauer, 1835: 96 [Type locality: “ Chile: Chiloe I.” (Bernhauer 1935)]. Distribution: Chile (Bernhauer 1835; Blackwelder 1944; Newton & Thayer 2005).Published as part of Silva, Sidnei Bortoluzzi Da & Caron, Edilson, 2014, The unique Brazilian species of Polylobus Solier (Coleoptera: Staphylinidae: Aleocharinae) with a checklist of all species of the genus, pp. 226-238 in Zootaxa 3811 (2) on page 232, DOI: 10.11646/zootaxa.3811.2.4, http://zenodo.org/record/22588
Nocticanace darwini Wirth 1969
darwini Wirth Nocticanace darwini Wirth, 1969b: 585. Wirth 1975: 3 [catalogue]; Linsley 1977: 41 [checklist]; Mathis 1992: 9 [catalogue]; Munari & Mathis 2010: 22 [catalogue]. Distribution. Endemic. Galápagos: Fernandina, Genovesa. Remarks. Adults of this species were reported nesting on the backs of crabs among intertidal rocks (Wirth 1969b).Published as part of Sinclair, Bradley J., 2023, An annotated checklist of the Diptera of the Galápagos Archipelago (Ecuador), pp. 1-102 in Zootaxa 5283 (1) on page 68, DOI: 10.11646/zootaxa.5283.1.1, http://zenodo.org/record/791266
Phyllotis darwini
Phyllotis darwini (Waterhouse, 1837). Proc. Zool. Soc. Lond., 1837:28. TYPE LOCALITY: Chile, Coquimbo Prov., Coquimbo. DISTRIBUTION: C Peru (Junfn), south through W Bolivia, to C Chile and WC Argentina. SYNONYMS: abrocodon, arenarius, boedeckeri, campestris, capito, chilensis, dichrous, fulvescens, glirinus, griseoflavus (of Philippi, 1900), illapelinus, lanatus, limatus, megalotis, melanotis, melanotus, mollis, platytarsus, posticalis, ricarulus, rupestris, segethi. COMMENTS: See accounts of P. bonaeriensis, P. caprinus, P. definitus, P. magister, P. osgoodi, P. wolffsohni, and P. xanthopygus, previously arrayed as subspecies of P. darwini by Pearson (1958) and /or Hershkovitz (1962), for references addressing their specific status. The complexity of populations comprising this species urges still further revisionary attention.Published as part of Guy G. Musser & Michael D. Carleton, 1993, Order Rodentia - Family Muridae, pp. 501-755 in Mammal Species of the World (2 nd Edition), Washington and London :Smithsonian Institution Press on page 738, DOI: 10.5281/zenodo.735309
Geospiza darwini Rothschild and Hartert
Geospiza darwini Rothschild and Hartert Geospiza darwini Rothschild and Hartert, 1899: 158 (Culpepper Island, Galapagos). Now Geospiza conirostris darwini Rothschild and Hartert, 1999. See Hellmayr, 1938: 130, Paynter, 1970b: 164, and Dickinson, 2003: 796. HOLOTYPE: AMNH 516980, adult male, collected on Darwin (5 Culpepper) Island, 01.39S, 92.00W (Paynter, 1993), Galapagos Islands, Ecuador, on 27 July 1897, by Rollo Beck on the Webster-Harris Expedition (no. 157). From the Rothschild Collection. COMMENTS: No type was designated in the text of the original description, where measurements were given for four males and one female, but Beck’s specimen no. 157 is designated as the type of Geospiza darwini in the same publication on pl. VI, fig. 21, a drawing of the beak of the holotype. Reference to this plate is also written on the reverse of the Rothschild type label of AMNH 516980. Paratypes in AMNH, all collected on Darwin Island on the Webster-Harris Expedition in 1897, are: AMNH 516977, adult male, 26 July, by Harris; AMNH 516978, adult male, 26 July, by Hull; AMNH 516979, immature male, 27 July, by Drowne; AMNH 516785, adult male, 27 July, by Beck, the last three now identified as magnirostris. I think that Rothschild and Hartert considered the immature bird to be a female. The right wing of that specimen is missing feathers, but the measurement of the left wing is 84 mm, the measurement given for the female.Published as part of LeCroy, Mary, 2012, Type Specimens Of Birds In The American Museum Of Natural History Part 10. Passeriformes: Emberizidae: Emberizinae, Catamblyrhynchinae, Cardinalinae, Thraupinae, And Tersininae, pp. 1-125 in Bulletin of the American Museum of Natural History 2012 (368) on page 39, DOI: 10.1206/775.1, http://zenodo.org/record/539945
Ropalidia darwini Richards 1978
darwini Richards Ropalidia darwini Richards, 1978: 61, 64 (key), 72, female, male (in subgenus Icariola) - “ Northern Territory, 12°25’S., 131°03’E., Milner’s Swamp” (holotype female Sydney); also from two other localities in Northern Territory. - Cardale, 1985: 214 (in subgenus Icariola; cat.). - Kojima & Carpenter, 1997a: 18 (cat.). - Kojima, 1999b: 369, Figs 13–14, 17 (W. A.); 1999c: 380 (key), 384 (distr.), Fig. 27. - Saito & Kojima, 2005a: 181, Figs 9–14 (in stigma group; N. T., W. A.). - Brown, 2009: 30 (North Coast). - Miličić et al., 2011: 524 (list). Distribution: N coastal; N. T., W. A.Published as part of Carpenter, James M. & Brown, Graham R., 2022, Catalogue of the Australian social wasps (Hymenoptera: Vespidae), pp. 451-495 in Zootaxa 5214 (4) on page 461, DOI: 10.11646/zootaxa.5214.4.1, http://zenodo.org/record/739761
Generating synthetic social graphs with Darwini
Synthetic graph generators facilitate research in graph algorithms and graph processing systems by providing access to graphs that resemble real social networks while addressing privacy and security concerns. Nevertheless, their practical value lies in their ability to capture important metrics of real graphs, such as degree distribution and clustering properties. Graph generators must also be able to produce such graphs at the scale of real-world industry graphs, that is, hundreds of billions or trillions of edges.In this paper, we propose Darwini, a graph generator that captures a number of core characteristics of real graphs. Importantly, given a source graph, it can reproduce the degree distribution and, unlike existing approaches, the local clustering coefficient distribution. Furthermore, Darwini maintains a number of metrics, such as graph assortativity, eigenvalues, and others. Comparing Darwini with state-of-the-art generative models, we show that it can reproduce these characteristics more accurately. Finally, we provide an open source implementation of Darwini on the vertex-centric Apache Giraph<sup>TM</sup>&nbsp;model that can generate synthetic graphs with up to 3 trillion edges.</jats:p
Camponotus darwini subsp. themistocles For.
Camponotus Darwini For. st. Themistocles For. Cette forme ne constitue qu'une race du Darwini tres voisine de robustior For. La [[worker]] maxima atteint 11 mill. La tete est plus large que le pronotum. L'epistome n'est plus carene chez le [[worker]] au-dessus de 10 mill. de long, comme du reste chez robustior For., mais en differe, comme l'indique M. Forel, par le pronotum plus anguleux, la face basale de l'epinotum plus longue et plus convexe. La pilosite beaucoup plus espacee (ne formant pas pelisse); par contre, il y a quelques poils fins dresses sous le bord inferieur des cuisses, et surtout par la ponctuation plus regu- liere, tandis qu'elle est presque reticulaire et transversale chez robustior. Madagascar. Region du sud. Andrahoumana. (Ch. Alluaud, 1901.) Museum de Paris.Published as part of Santschi, F., 1911, Nouvelles fourmis de Madagascar., pp. 117-134 in Revue Suisse de Zoologie 19 on pages 133-13
Nesoryzomys darwini Osgood 1929
Nesoryzomys darwini Osgood, 1929. Field Mus. Nat. Hist. Pubi., Zool. Ser., 17:23. TYPE LOCALITY: Ecuador, Galapagos Archipelago, Santa Cruz Island, Academia Bay. DISTRIBUTION: Santa Cruz (= Indefatigable) Island. COMMENTS: Probably extinct, last recorded in 1930 (see Patton and Hafner, 1983).Published as part of Guy G. Musser & Michael D. Carleton, 1993, Order Rodentia - Family Muridae, pp. 501-755 in Mammal Species of the World (2 nd Edition), Washington and London :Smithsonian Institution Press on page 713, DOI: 10.5281/zenodo.735309
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