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FIGURE 11 in A revision of "Trinitichelys" maini (Testudinata: Baenidae) and additional material of its new genus from the Lewisville Formation (Woodbine Group, Cenomanian), Texas, USA
FIGURE 11. Results of phylogenetic analyses for Gehennachelys maini comb. nov., produced from the modified matrix Rollot et al. (2022b), with 170 minimum trees and 367 steps (CI= 0.35; RI= 0.71): A) Consensus 50% majorityrule phylogenetic tree of Baenidae; B) Strict consensus tree. Yellow stars indicate Gehennachelys maini comb. nov.
Figure 1. – Gobius xoriguer. A in The Adriatic record of Gobius xoriguer Iglésias, Vukić & Šanda, 2021 and additional records of Vanneaugobius dollfusi Brownell, 1978 (Actinopterygii: Gobiiformes: Gobiidae)
Figure 1. – Gobius xoriguer. A: Male, 47.7 mm, caudal fin damaged, PMR VP5427, South Adriatic Sea. B: Female, 53.3 + 12.2 mm, PMR VP5426, North Adriatic Sea. Preserved specimens (photo M. Kovačić).
Рис. 1. 1 — Eriogyna koreanis (Brechlin, 2009) (Saturniidae), ♂, Казакевичево, из коΛΛекции ЗооΛогического иссΛеΑоватеΛьского музея АΛексанΑра Кёнига (Германия). Фото В. В. ЗоΛотухина; 2 — Nola confusalis; 3 — Negritothripa hampsoni; 4 — Autographa urupina; 5 — Athetis lapidea; 6–7 — Euplexia koreaeplexia; 8 — Nonagria puengeleri; 9 — Lacanobia oleracea; 10 —Actebia squalida Fig. 1. 1 — Eriogyna koreanis (Brechlin, 2009) (Saturniidae), ♂, Kazakevichevo (Kassakewitschevo), collection of the Zoological Research Museum Alexander Koenig (Germany). Photo by V. V. Zolotuhin; 2 — Nola confusalis; 3 — Negritothripa hampsoni; 4 — Autographa urupina; 5 — Athetis lapidea; 6–7 — Euplexia koreaeplexia; 8 — Nonagria puengeleri; 9 — Lacanobia oleracea; 10 —Actebia squalida in Additions To The Macromoth Fauna (Insecta, Lepidoptera, Macroheterocera) Of Bolshekhekhtsyrsky Nature Reserve (Khabarovsky Krai)
Рис. 1. 1 — Eriogyna koreanis (Brechlin, 2009) (Saturniidae), ♂, Казакевичево, из коΛΛекции ЗооΛогического иссΛеΑоватеΛьского музея АΛексанΑра Кёнига (Германия). Фото В. В. ЗоΛотухина; 2 — Nola confusalis; 3 — Negritothripa hampsoni; 4 — Autographa urupina; 5 — Athetis lapidea; 6–7 — Euplexia koreaeplexia; 8 — Nonagria puengeleri; 9 — Lacanobia oleracea; 10 —Actebia squalida Fig. 1. 1 — Eriogyna koreanis (Brechlin, 2009) (Saturniidae), ♂, Kazakevichevo (Kassakewitschevo), collection of the Zoological Research Museum Alexander Koenig (Germany). Photo by V. V. Zolotuhin; 2 — Nola confusalis; 3 — Negritothripa hampsoni; 4 — Autographa urupina; 5 — Athetis lapidea; 6–7 — Euplexia koreaeplexia; 8 — Nonagria puengeleri; 9 — Lacanobia oleracea; 10 —Actebia squalida
BOLD5000 Additional ROIs and RDMs for neural network research
<p>Artificial neural networks (ANNs) are sensitive to perturbations and adversarial attacks. One hypothesized solution to adversarial robustness is to align manifolds in the embedded space of neural networks with biologically grounded manifolds. Recent state-of-the-art works that emphasize learning robust neural representations, rather than optimizing for a specific target task like classification, support the idea that researchers should investigate this hypothesis. While works have shown that fine-tuning ANNs to coincide with biological vision does increase robustness to both perturbations and adversarial attacks, these works have relied on proprietary datasets- the lack of publicly available biological benchmarks make it difficult to evaluate the efficacy of these claims. Here, we deliver a curated dataset consisting of biological representations of images taken from two commonly used computer vision datasets, ImageNet and COCO, that can be easily integrated into model training and evaluation. Specifically, we take a large functional magnetic resonance imaging (fMRI) dataset (BOLD5000), preprocess it into representational dissimilarity matrices (RDMs), and establish an infrastructure that anyone can use to train models with biologically grounded representations. Using this infrastructure, we investigate the representations of several popular neural networks and find that as networks have been optimized for tasks, their correspondence with biological fidelity has decreased. Additionally, we use a previously unexplored graph-based technique, Fiedler partitioning, to showcase the viability of the biological data, and the potential to extend these analyses by extending RDMs into Laplacian matrices. Overall, our findings demonstrate the potential of utilizing our new biological benchmark to effectively enhance the robustness of models.</p>
Fig. 3 in A new species of Zorochros from Iran, with additional records and an updated checklist of Iranian species of this genus (Coleoptera: Elateridae, Negastriinae)
Fig. 3 – Zorochros murinus (Reitter, 1895), female. a, Dorsal habitus; b, internal genitalia, spermatheca; c, internal genitalia, ovipositor.
Fig. 1 in A new species of Zorochros from Iran, with additional records and an updated checklist of Iranian species of this genus (Coleoptera: Elateridae, Negastriinae)
Fig. 1 – Zorochros parvus sp. nov., male holotype. a, Dorsal habitus; b, aedeagus, dorsal view, photography by compound microscope, 40×; c, aedeagus, dorsal view, photography by compound microscope, 10×.
Fig. 11 in Additions to the Ammonite Fauna of the Upper Cretaceous Navesink Formation of New Jersey
Fig. 11. Jeletzkytes cf. J. nodosus (Owen, 1852), MAPS A2020a2, microconch, lower phosphatic level, Navesink Formation, Atlantic Highlands, New Jersey. All figures are X1.
Fig. 9. A–F in Additions to the Ammonite Fauna of the Upper Cretaceous Navesink Formation of New Jersey
Fig. 9. A–F. Hoploscaphites pumilus (Stephenson, 1941). A, B. MAPS 2032a1; C, D. MAPS 2032a2; E, F. MAPS 2032a3; G–I. Discoscaphites gulosus (Morton, 1834), NJSM 16121, Inversand Pit, Sewell, Gloucester County, New Jersey. J–P. Jeletzkytes cf. J. nodosus (Owen, 1852). J–L. MAPS A2020a3; M, N. MAPS A2020a5; O, P. MAPS A2020a4. All specimens are from the lower phosphatic layer, Navesink Formation, Atlantic Highlands, unless otherwise stated. All figures are X1.
Fig. 5. A–E, K–O in Additions to the Ammonite Fauna of the Upper Cretaceous Navesink Formation of New Jersey
Fig. 5. A–E, K–O. Nostoceras (Nostoceras) approximans (Conrad, 1855). A, B. MAPS A2027a2, macroconch; C–E. holotype, ANSP 12861, microconch, White River, Arkansas; K–M. MAPS 2027a1, microconch; N, O. USNM 445246, pathological microconch. F–H. Exiteloceras rude, n. sp., holotype, USNM 433778, Big Brook, near Marlboro, Monmouth County. I, J. Didymoceras cf. D. draconis (Stephenson, 1941), MAPS A2040b1. All specimens are from the lower phosphatic layer, Navesink Formation, Atlantic Highlands, New Jersey, unless otherwise stated. All figures are X1.
Fig. 2 in Additions to the Ammonite Fauna of the Upper Cretaceous Navesink Formation of New Jersey
Fig. 2. Locality map for part of New Jersey showing localities where Navesink ammonites were collected.
Fig. 10 in Additions to the Ammonite Fauna of the Upper Cretaceous Navesink Formation of New Jersey
Fig. 10. Jeletzkytes cf. J. nodosus (Owen, 1852), MAPS A2020a1, macroconch, lower phosphatic level, Navesink Formation, Atlantic Highlands, New Jersey. Both figures are X1.
Fig. 12. A, B. Jeletzkytes criptonodosus Riccardi, 1983, MAPS A2050a1 in Additions to the Ammonite Fauna of the Upper Cretaceous Navesink Formation of New Jersey
Fig. 12. A, B. Jeletzkytes criptonodosus Riccardi, 1983, MAPS A2050a1, Navesink Formation, bank of Nut Swamp Brook, near Middletown, Monmouth County. C–F. Jeletzkytes cf. J. nodosus (Owen, 1852), lower phosphatic layer, Navesink Formation, Atlantic Highlands, New Jersey. C. USNM 445247; D, E. MAPS A2020a6; F. MAPS A2020a7. All figures are X1.
Fig. 1 in First records of Cixidia maroccana Anufriev, 1969 from the Iberian Peninsula and some additional new records of Achilidae Stṏl, 1839 (Auchenorrhyncha: Fulgoromorpha)
Fig. 1.- Adult female of Cixidia cf. lapponica, 1.5 km northeAst of L'Ampolla (Tarragona, Spain), 28.IV.2023. Photo: M.C. de Haas.
Fig. 4 in First records of Cixidia maroccana Anufriev, 1969 from the Iberian Peninsula and some additional new records of Achilidae Stṏl, 1839 (Auchenorrhyncha: Fulgoromorpha)
Fig. 4.- Habitat of place where nymphs and adults of Cixidia maroccana were found, Quinta de Marim (Olhão, Portugal). Photo: T. Valkenburg.
Fig. 2 in Anthidium manicatum (Linnaeus, 1758) (Hymenoptera; Megachilidae), an addition to the wild bee fauna of Madeira Island (Portugal)
Fig. 2.- Anthidium manicatum ♀, 01/10/2021, Parque de Santa Catarina, Funchal, Madeira, 115 m west of Capela de SAntA CAtArinA, 32° 38' 44,6" N, 16° 54' 52,3" E. (Photo; G. Matzke-Hajek).
Fig. 1 in Anthidium manicatum (Linnaeus, 1758) (Hymenoptera; Megachilidae), an addition to the wild bee fauna of Madeira Island (Portugal)
Fig. 1.- Anthidium manicatum ♀, 01/10/2021, Parque de Santa Catarina, Funchal, Madeira, near the Cristóvão Colombo statue, 32° 38' 44,2" N, 16° 54' 48,2" E. (Photo: G. MAtzke-Hajek).
Fig. 3 in Anthidium manicatum (Linnaeus, 1758) (Hymenoptera; Megachilidae), an addition to the wild bee fauna of Madeira Island (Portugal)
Fig. 3.- Locality of Anthidium observations in Parque de Santa Catarina, Funchal, Madeira, viewing direction eastwards with the white Capela building in middle distance. A bed of Salvia leucantha (= picture position of Fig. 2) in the foreground. (Photo; G. Matzke-Hajek).
Fig. 1 in Short Communication Additional notes on the herpetofauna of Lefkada (Ionian Islands, Greece)
Fig. 1 - The islands of Lefkada and Meganissi in western Greece. Four notable reptile species are illustrated whose occurrence locations are marked on the map A) Testudo hermanni (near Nikiana, 24/6/2023), B) T. marginata (near Rachi/Perigiali, 5/10/2022), C) Platyceps najadum (Nikiana, hotel grounds, 11/10/2022), D) Telescopus fallax, young specimen (near Nikiana, 30/6/2023). / Le isole di Lefkada e Meganissi, nella Grecia occidentale. Sono illustrate quattro specie rilevanti di rettili, le cui località di ritrovamento sono indicate sulla mappa A) Testudo hermanni (vicino a Nikiana, 24/6/2023), B) T. marginata (vicino a Rachi/Perigiali, 5/10/2022), C) Platyceps najadum (Nikiana, terreno dell'hotel, 11/10/2022), D) Telescopus fallax, giovane esemplare (vicino a Nikiana, 30/6/2023). (Photo / Foto: M. Schmitt).
Fig. 14. A in Early summer aspect of butterflies (Lepidoptera: Papilionoidea) of Republic of Khakassia as examined in 2000, with some additional data
Fig. 14. A male of Oeneis aktashi ona on a scree at the Sayanskiy Pass, 7.07.2000 Рис. 14. Самец Oeneis aktashi ona на осыпи в окрестностях Саянского переваΛа, 7.07.2000
Fig. 13. A in Early summer aspect of butterflies (Lepidoptera: Papilionoidea) of Republic of Khakassia as examined in 2000, with some additional data
Fig. 13. A male of Plebejus idas subsolanus at Tashtyp Village, 6.07.2000 Рис. 13. Самец Plebejus idas subsolanus в окрестностях с. Таштып, 6.07.2000
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.