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Figures 1−9 in New data on Neotropical Carpenter-Moths of Subfamily Hypoptinae Neumoegen & Dyar, 1894 (Lepidoptera: Cossidae). II. A review of the genus Dolecta Herrich-Schäffer, [1854], with description of seventeen new species
Figures 1−9. Dolecta, adults: 1. D. akhmatovae sp. nov., male, holotype, Brasilien, Esp. Santo, Santa Leopoldina, Biriricas (MWM); 2. D. amanosa (Schaus, 1911) comb. nov., male, holotype, Tuis, C.R. (USNM); 3. D. aroa (Schaus, 1894) comb. nov., male, holotype, Aroa, Venezuela (USNM); 4. D. aroa (Schaus, 1894) comb. nov., male, Ecuador, Esmeraldes prov., 3.2 km E Mompiche (MWM); 5. D. aroa (Schaus, 1894) comb. nov., male, Brasil, Bahia, env. Camacan (SB) (MWM); 6. D. aroa (Schaus, 1894) comb. nov., male, NW Argentina, Jujuy Prov., 10 km SEE Caimancito (RYB); 7. D. aroa (Schaus, 1894) comb. nov., female, Brasil, Bahia, env. Camacan (MWM); 8. D. bulgakovi sp. nov., male, holotype, Guyane Franc., Saül (MNHN); 9. D. chekhovi sp. nov., male, holotype, Peru, prov. Huánuco, Yuyapichis, ACP Panguana (MWM).
Figures 5−7 in New data on Neotropical Carpenter Moths of Subfamily Hypoptinae Neumoegen & Dyar, 1894 (Lepidoptera: Cossidae). III. Laberlia - a new genus from Northern and Central Andean Mountains
Figures 5−7. Laberlia, male genitalia: 5. L. bellaria (Dognin, 1911) comb. nov., male, Colombia, Tolima, Cerro Bravo, La Libia, 5°06′21"N 75°16′22"W, 3000 m, 03-04.XI.2015 (Genital preparation №142 coll. Naydenov A.E.) (RYB); 6. L. illapai sp. nov., male, holotype, Ecuador, Morona Santiago, 55 km Road Rio Bamba-Macas, 2°11'04"S 78°29'51"W, 3470 m, 24.III.2012 (Genital preparation №321 coll. Naydenov A.E.) (ZISP); 7. L. apusorum sp. nov., male, holotype, Peru, La Libertad, Pataz prov., S of Tayabamba, 3840 m, 08°23.18'S 77°16.39'W, 17.XII.2016 (Genital preparation №331 coll. Naydenov A.E.) (ZISP).
Figures 1−4 in New data on Neotropical Carpenter Moths of Subfamily Hypoptinae Neumoegen & Dyar, 1894 (Lepidoptera: Cossidae). III. Laberlia - a new genus from Northern and Central Andean Mountains
Figures 1−4. Laberlia, adults: 1. L. bellaria (Dognin, 1911) comb. nov., male, holotype, Colombia, Quindío Department, Páramo, 3800 m (USNM); 2. L. bellaria (Dognin, 1911) comb. nov., male, Colombia, Tolima, Cerro Bravo, La Libia, 5°06′21"N 75°16′22"W, 3000 m, 03-04.XI.2015 (RYB); 3. L. illapai sp. nov., male, holotype, Ecuador, Morona Santiago, 55 km Road Rio Bamba-Macas, 2°11'04"S 78°29'51"W, 3470 m, 24.III.2012 (ZISP); 4. L. apusorum sp. nov., male, holotype, Peru, La Libertad, Pataz prov., S of Tayabamba, 3840 m, 08°23.18'S 77°16.39'W, 17.XII.2016 (ZISP).
FIGURES 9−15 in A new monotypic genus of the subfamily Chilecomadiinae Dyar, 1940 (Lepidoptera: Cossidae) from South America
FIGURES 9−15. Cossidae, male, genitalia: 9. Miacorella leucocraspedontis (Zukowsky, 1954), neotype, male, Peru: Apurimac, Abancay, 26.11.2010, leg. Viktor & Svetlana Sinyaev + Yury Bezverkhov (Gen. prep. №18, Naydenov A.E.), (RYB); 10. M. leucocraspedontis (Zukowsky, 1954), male, Bolivia: Cochabamba, Zischka leg. (Prep.Gen. MLP Nº5), (MLP); 11. M. leucocraspedontis (Zukowsky, 1954), male, Argentina: Tucumán, La Viña, 30 Ene 1998, leg. J.Rumi (Prep.Gen.Het.№ 26.716), (MWM); 12. Miacora tropicalis (Schaus, 1904), male, Central Peru, Villa Rica-Pto Bermudez, 12.III.2013, leg. V. V. Doroshkin (RYB); 13. Chilecomadia moorei (Silva Figueroa, 1915), male, ARGENTINIEN, Cafayate, Prov. Catamarca, 16.XII.98, Leg. A. Ugarte P. (MWM), (Prep.Gen.Het.№ 26.780); 14. Chilecomadia valdiviana (Philippi, 1859), male, Argentinien, Patagonien prov. Rio Negro, Carlos de Bariloche, XII.2005.III.2006, leg. Local collectors (MWM), (Prep.Gen.Het.№ 26.728); 15. Rhizocossus munroei Clench, 1957, male, Chile prov. Nuble, Shangrila, XII.1998, leg. A. Ugarte P. (MWM), (Prep.Gen.Het.№ 28.477).
FIGURES 1−8 in A new monotypic genus of the subfamily Chilecomadiinae Dyar, 1940 (Lepidoptera: Cossidae) from South America
FIGURES 1−8. Cossidae, adults: 1. Miacorella leucocraspedontis (Zukowsky, 1954), neotype, male, Peru: Apurimac, Abancay, 26.11.2010, leg. Viktor & Svetlana Sinyaev + Yury Bezverkhov (RYB); 2. M. leucocraspedontis (Zukowsky, 1954), male, Bolivia: Cochabamba, Zischka leg. (MLP); 3. M. leucocraspedontis (Zukowsky, 1954), male, Argentina: Tucumán, La Viña, 30 Ene 1998, leg. J. Rumi (MWM); 4. M. leucocraspedontis (Zukowsky, 1954), female, Argentina: Salta, San Lorenzo, Oct 1950, P. Kohler leg. (FML); 5. Miacora tropicalis (Schaus, 1904), male, Central Peru, Villa Rica-Pto Bermudez, 12.III.2013, leg. V.V. Doroshkin (RYB); 6. Chilecomadia moorei (Silva Figueroa, 1915), male, ARGENTINIEN, Cafayate, Prov. Catamarca, 16-11-98, leg. A. Ugarte P. (Prep.Gen.Het.№ 26.780) (MWM); 7. Chilecomadia valdiviana (Philippi, 1859), male, Argentinien, Patagonien prov. Rio Negro, Carlos de Bariloche, XII.2005-III.2006, leg. Local collectors (Prep.Gen.Het.№ 26.728) (MWM); 8. Rhizocossus munroei Clench, 1957, male, Chile prov. Nuble, Shangrila, XII.1998, leg. A. Ugarte P. (Prep.Gen.Het.№ 28.477) (MWM).
Figure 4 in A surprising finding of Ecclisopteryx asterix Malicky, 1979 (Insecta, Trichoptera) in Croatia with notes to DNA barcoding and new distributional data of the subfamily Drusinae
Figure 4. Spatial distribution of the Drusinae species in Croatia, literature data supplemented with new records.
Figure 3 in A surprising finding of Ecclisopteryx asterix Malicky, 1979 (Insecta, Trichoptera) in Croatia with notes to DNA barcoding and new distributional data of the subfamily Drusinae
Figure 3. Maximum likelihood phylogram based on the COI sequences of Ecclisopteryx asterix from Croatia and haplotypes of Ecclisopteryx species available in BOLD database. Numbers at the nodes indicate maximum likelihood (ML) bootstrap support values (BS). Terminal codes represent BOLD Process IDs.
Figure 2. A in A surprising finding of Ecclisopteryx asterix Malicky, 1979 (Insecta, Trichoptera) in Croatia with notes to DNA barcoding and new distributional data of the subfamily Drusinae
Figure 2. A Larva of Ecclisiopteryx asterix in its case; B morphological character important for identification: shape of the pronotum (p); C pronotum (p), mesonotum (me), and sclerites at metanotum (mt) in dorsal view; D abdominal segments I-VI with gills (g) and lateral fringe (lf), right lateral view.
Figure 1. A in A surprising finding of Ecclisopteryx asterix Malicky, 1979 (Insecta, Trichoptera) in Croatia with notes to DNA barcoding and new distributional data of the subfamily Drusinae
Figure 1. A New record of Ecclisopteryx asterix Malicky, 1979 in Croatia (red dot) and hitherto known range in Austria, Slovenia and Italy (yellow area) (Robert, 2015); B the crenal reach of the Šumi Spring, and C a close up of the habitat where E. asterix larvae were collected.
Figures 10−14 in New data on Neotropical Carpenter-Moths of Subfamily Hypoptinae Neumoegen & Dyar, 1894 (Lepidoptera: Cossidae). IV. A review of the genus Hypopta Hübner, 1818
Figures 10−14. Hypopta, male genitalia: 10. H. ambigua Hübner, 1818, male, Argentina, Chaco, San Bernardo, Chaco, San Bernardo, 20.I.1980 (Genital preparation №269 coll. Naydenov A.E.) (RYB); 11. H. ambigua Hübner, 1818, male, Argentina, Tornquist, "J.R.", 22.II.1993 (Genitalpräparat Heterocera № 26.729) (MWM); 12. H. guarani Penco, Yakovlev & Naydenov sp. nov., male, holotype, Paraguay, Dep. Alto Paraná, Estancia Dimas, S 25°33′ W 55°13′, 10- 12.II.2018, leg. U. Drechsel (Genital preparation №264 coll. Naydenov A.E.) (ZISP); 13. H. invetita (Dognin, 1923), male, Argentina, La Viña, 12.I.1994, leg. J. R[umi] (Genitalpräparat Heterocera № 26.746) (MWM); 14. H. watsoni (Schaus, 1901), male, Brazil, Bahia, Jequié, S 13°56′ W 40°11′, III.2012, leg. Hubert Thöny (Genitalpräparat Heterocera № 28.637) (MWM).
Figures 1−9 in New data on Neotropical Carpenter-Moths of Subfamily Hypoptinae Neumoegen & Dyar, 1894 (Lepidoptera: Cossidae). IV. A review of the genus Hypopta Hübner, 1818
Figures 1−9. Hypopta, adults: 1. H. ambigua Hübner, 1818, male, holotype of Endagria tigrina Boisduval, 1859, B[?]ayses, ex musaeo Boisduval (MNHN); 2. H. ambigua Hübner, 1818, male, Argentina, Tornquist, "J.R.", 22.II.1993 (MWM); 3. H. ambigua Hübner, 1818, female, Argentina, Chaco, San Bernardo, 12.I.1980, leg. O. Di Iorio (RYB); 4. H. guarani Penco, Yakovlev & Naydenov sp. nov., male, holotype, Paraguay, Dep. Alto Paraná, Estancia Dimas, S 25°33′ W 55°13′, 10-12.II.2018, leg. U. Drechsel (ZISP); 5. H. guarani Penco, Yakovlev & Naydenov sp. nov., male, paratype, Paraguay, Dep. Cordillera, Pirareta, S 25°29′ W 56°56′, 16 -18.III.2012, leg. U. Drechsel (RYB); 6. H. invetita (Dognin, 1923), female, holotype of Philanglaus invetita, Argentina, Cordoba, Type №29899 (USNM); 7. H. invetita (Dognin, 1923), male, Argentina, La Viña, 12.I.1994, leg. J. R[umi] (MWM); 8. H. watsoni (Schaus, 1901), male, holotype of Givira watsoni Schaus, 1901, Brazil, Bnito Prov., Pernambuco, Type №18594 (USNM); 9. H. watsoni (Schaus, 1901), male, Brazil, Bahia, Jequié, S 13°56′ W 40°11′, III.2012, leg. Hubert Thöny (MWM).
Fig. 4 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites
Fig. 4. Mature sporocysts of Hyaloklossia in the kidney of Pelophylax porosus porosus. (A) Light microscopy of a mature sporocyst in homogenized kidney tissue. (B) Nomarski interference contrast microscopy of a mature sporocyst in squash preparation of renal tubular tissue showing the presence of four spindle-shaped sporozoites. (C) Composite line drawing. Bar = 10 μm. Asterisk: sporocyst residuum.
Fig. 3 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites
Fig. 3. Light microscopy of hematoxylin and eosin-stained sections of renal tissues of Pelophylax porosus porosus. (A) Mature sporocysts in the renal interstitium. Arrows indicate the transverse section of sporocysts showing four sporozoites with nuclei and a granular sporocyst residuum. (B and C) Immature oocysts. Note the very thin oocyst wall (arrows), sporonts with granular cytoplasm, and nuclei distributed at the cell margin (arrowheads). (D) Immature oocysts with two sporoblasts each and containing two polar nuclei (arrowheads). (E) Mature oocysts in renal epithelial cell showing two sporocysts with elongated sporozoites with circular nuclei (arrowhead) and a granular sporocyst residuum. Arrows indicate the sporocyst wall. Bars = 50 μm (A) and 10 μm (B–E).
Fig. 2 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites
Fig. 2. Light microscopy of hematoxylin and eosin-stained sections of renal tissue of Pelophylax porosus porosus. Hyaloklossia sporocysts and/or oocysts congregated in a diffused manner in the renal interstitium (circles), and some were found solitarily in renal epithelial cells or in the lumen (arrowheads). Bar = 200 μm. A highresolution version of this slide for use with the Virtual Microscope is available as eSlide: VM06312.
Fig. 5 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites
Fig. 5. Phylogenetic trees of coccidian parasites belonging to the subfamilies Toxoplasmatinae, Eumonosporinae, and Cystoisosporinae and related taxa using 18S (A), 28S (B), and cox1 (C) sequence data. Sarcocystis rileyi (Sarcocystidae: Sarcocytinae) was used as an outgroup. The nodes are labeled using support from the bootstrap values obtained for neighbor joining (left) and maximum likelihood (right) methods. The unlabeled nodes and hyphens indicate support <50. Scale bars represent the substitutions per site.
Fig. 1 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites
Fig. 1. Light microscopy of Hyaloklossia sporocysts in the kidney of Pelophylax porosus porosus. (A) Mature sporocysts within a cyst-like structure are visible in the renal interstitium. (B) Squash preparation of kidney showing numerous immature sporocysts. Note the granular cytoplasm of the sporoblasts (sporonts) and the barely visible membrane surrounding them. (C) A sporocyst (arrowhead) in the renal endothelial cell. (D) Mature oocyst (arrowhead) with two sporocysts in the renal endothelial cell. Asterisk indicates renal tubules. Bars = 25 μm.
Fig. 6 in New dental elements of the oldest proviverrine mammal from the early Eocene of Southern France support possible African origin of the subfamily
Fig. 6. Comparison of phylogenetic trees and of the three hypotheses of hyaenodont origin and dispersals with focus on the Sinopinae and Proviverrinae. A. African origin with subsequent dispersals of the Sinopinae and Proviverrinae into Europe, and of the Sinopinae from Europe to North America. A 1. The phylogenetic tree based on the cladistics analysis of Solé et al. (2014b). A 2. Faunal dispersals during the early Eocene based on the hypothesis of an African origin for the Hyaenodonta. B. Asian origin with subsequent dispersals of Sinopinae and Proviverrinae into Europe, and of Tinerhodon from Europe to Africa. B 1. The phylogenetic tree based on the cladistics analysis of Rana et al. (in press); the position of the Group A is variable—we represent only two of the four possible positions: the basal position implies two dispersal events from Laurasia to Africa, while the more inclusive position implies one single event. B 2. Faunal dispersals around the Paleocene–Eocene transition based on the hypothesis of an Asian origin for the Hyaenodonta. C. Multiregional origin with subsequent dispersals of the Sinopinae from Asia to North America through Europe, and of the Proviverrinae from Africa to Europe. C 1. The phylogenetic tree based on the abstract of Morlo et al. (2010). C 2. Faunal dispersals during the early Eocene based on the hypotheses of an Asian origin for the Sinopinae (Hyaenodontida) and of an African one for the Proviverrinae (Proviverroidea). The phylogeny of Rana et al. in press) is, however, consistent with either an African or an Asian origin for the Hyaenodonta; only the Asian origin is discussed here; the position of Tinerhodon in C 1 is our hypothesis because this taxon is not discussed by Morlo et al. (2010). Abbreviations: A, Africa; L, Laurasia. Bolded, taxa that mainly radiated in Africa; asterisks, paraphyletic subfamilies in Rana et al. (in press). A 2 –C 2 are adapted from Ron Blakey, Eocene, http://www2.nau. edu/rcb7/050Marect.jpg.
Fig. 4. Proviverrine mammal Eoproviverra eisenmanni Godinot, 1981 in New dental elements of the oldest proviverrine mammal from the early Eocene of Southern France support possible African origin of the subfamily
Fig. 4. Proviverrine mammal Eoproviverra eisenmanni Godinot, 1981 from early Eocene, Rians, France; MNHN.F.RI 400, left m2; labial (A), occlusal (B), and lingual (C) views.
Fig. 7 in New dental elements of the oldest proviverrine mammal from the early Eocene of Southern France support possible African origin of the subfamily
Fig. 7. Geographic localisation of the Asian hyaenodonts mentioned in the text, and distributions of the Limnocyoninae and Indohyaenodontinae. Both the geographic distributions of the Limnocyoninae and Indohyaenodontinae include the Mongolian specimen PSS 20-124. Adapted from Ron Blakey, Eocene, http://www2.nau.edu/rcb7/050Marect.jpg.
Fig. 3 in New dental elements of the oldest proviverrine mammal from the early Eocene of Southern France support possible African origin of the subfamily
Fig. 3. Proviverrine mammal Parvagula palulae Lange-Badré in Godinot et al., 1987 from Fournes (A, C, D) and Fordones (B), France, early Eocene. A. UM/FNR 53, right fragmentary dentary bearing p4; labial (A 1), lingual (A2), and occlusal (A3) views. B. UM/FDN 153, left trigonid of m1?; occlusal (B 1), labial (B2), and lingual (B3) views. C. UM/FNR 52, left trigonid of m1?; occlusal (C1), labial (C2), and lingual (C3) views. D. UM/FNR 51, right m1?; labial (D 1), occlusal (D2), and lingual (D3) views. The frame distinguishes the sole specimen from Fordones.
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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)
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DANDI Archive for NWB datasets
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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.