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Linked collectors and determiners for: Type specimens and type localities of birds (Aves) collected during F. J. F. Meyen's circumnavigation in 1830 – 1832.

Natural history specimen data linked to collectors and determiners held within, "Type specimens and type localities of birds (Aves) collected during F. J. F. Meyen's circumnavigation in 1830 – 1832". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/ac9cc78c-c2cd-453f-8715-8f38648de567">https://bionomia.net/dataset/ac9cc78c-c2cd-453f-8715-8f38648de567</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/ac9cc78c-c2cd-453f-8715-8f38648de567">https://gbif.org/dataset/ac9cc78c-c2cd-453f-8715-8f38648de567</a>. Formatted as a Frictionless Data package.

Linked collectors and determiners for: Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species.

Natural history specimen data linked to collectors and determiners held within, "Solenoptera Audinet-Serville, 1832 (Coleoptera, Cerambycidae, Prioninae, Solenopterini) in Cuba, with description of a new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/941d5e15-8d4e-45f5-9d9e-1c0f670b045f">https://bionomia.net/dataset/941d5e15-8d4e-45f5-9d9e-1c0f670b045f</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/941d5e15-8d4e-45f5-9d9e-1c0f670b045f">https://gbif.org/dataset/941d5e15-8d4e-45f5-9d9e-1c0f670b045f</a>. Formatted as a Frictionless Data package.

opencc-zeroMar 2024View details →

Linked collectors and determiners for: First records of Isthmocoris piceus (Say, 1832) (Hemiptera: Geocoridae) in the Province of Quebec.

Natural history specimen data linked to collectors and determiners held within, "First records of Isthmocoris piceus (Say, 1832) (Hemiptera: Geocoridae) in the Province of Quebec". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/eb45d466-5140-4d12-8730-07f3dca49f86">https://bionomia.net/dataset/eb45d466-5140-4d12-8730-07f3dca49f86</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/eb45d466-5140-4d12-8730-07f3dca49f86">https://gbif.org/dataset/eb45d466-5140-4d12-8730-07f3dca49f86</a>. Formatted as a Frictionless Data package.

opencc-zeroApr 2024View details →

Linked collectors and determiners for: Studies in the New World tribe Anisoscelini Laporte, 1832 (Heteroptera: Coreidae: Coreinae): updated distributions, nomenclatural changes, and keys to the genera of the tribe and the species of Anisoscelis Latreille, 1829 and Bitta Osuna, 1984.

Natural history specimen data linked to collectors and determiners held within, "Studies in the New World tribe Anisoscelini Laporte, 1832 (Heteroptera: Coreidae: Coreinae): updated distributions, nomenclatural changes, and keys to the genera of the tribe and the species of Anisoscelis Latreille, 1829 and Bitta Osuna, 1984". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9ea2bb32-7f5e-4b32-ba7d-ee6a0c7baf43">https://bionomia.net/dataset/9ea2bb32-7f5e-4b32-ba7d-ee6a0c7baf43</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9ea2bb32-7f5e-4b32-ba7d-ee6a0c7baf43">https://gbif.org/dataset/9ea2bb32-7f5e-4b32-ba7d-ee6a0c7baf43</a>. Formatted as a Frictionless Data package.

Linked collectors and determiners for: Las colecciones de Johann Rudolph Rengger (1795 - 1832) en Argentina, Brasil y Paraguay. III. Tipificación de los nombres descritos a partir de los herbarios Rengger.

Natural history specimen data linked to collectors and determiners held within, "Las colecciones de Johann Rudolph Rengger (1795 - 1832) en Argentina, Brasil y Paraguay. III. Tipificación de los nombres descritos a partir de los herbarios Rengger". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/75aea3f5-8a27-4c1f-b9ed-61d4b132c450">https://bionomia.net/dataset/75aea3f5-8a27-4c1f-b9ed-61d4b132c450</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/75aea3f5-8a27-4c1f-b9ed-61d4b132c450">https://gbif.org/dataset/75aea3f5-8a27-4c1f-b9ed-61d4b132c450</a>. Formatted as a Frictionless Data package.

Linked collectors and determiners for: A molecular phylogeny and revision of the genus Pyropteron Newman, 1832 (Lepidoptera, Sesiidae) reveals unexpected diversity and frequent hostplant switch as a driver of speciation.

Natural history specimen data linked to collectors and determiners held within, "A molecular phylogeny and revision of the genus Pyropteron Newman, 1832 (Lepidoptera, Sesiidae) reveals unexpected diversity and frequent hostplant switch as a driver of speciation". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/cdd9688e-9a3f-4602-992e-1f8693caab9b">https://bionomia.net/dataset/cdd9688e-9a3f-4602-992e-1f8693caab9b</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/cdd9688e-9a3f-4602-992e-1f8693caab9b">https://gbif.org/dataset/cdd9688e-9a3f-4602-992e-1f8693caab9b</a>. Formatted as a Frictionless Data package.

FIG. 6 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 6. — Simpson's ratio diagram, comparing the means of the hypodigm sample of MCIII from Perpignan (own data) with single specimen from Ptolemais (data Koufos 1982: 232, table). Standard (in common logs) and measurements (in mm): 1, length 2.29; 2, proximal breadth 1.63; 3, proximal diameter 1.485; 4, diameter of proximal articular surface 1.445; 5, distal articular breadth 1.59; 6, distal protuberance breadth 1.63; 7, distal keel diameter 1.48; 8, midshaft breadth 1.49.

FIG. 11 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 11. — Simpson's ratio diagram, comparing the means of the hypodigm sample of MTIII from Perpignan (data own and Samson 1975: table 8) with sample means of Hipparion theobaldi Lydekker, 1877 from Dhok Pathan, Siwaliks (own data) and with single specimen from Roussillon. Standard (in common logs) and measurements (in mm): 1, length 2.36; 2, proximal breadth 1.63; 3, proximal diameter 1.55; 4, diameter of proximal articular surface 1.50; 5, distal articular breadth 1.58; 6, distal protuberance breadth 1.62; 7, distal keel diameter 1.50; 8, midshaft breadth 1.47.

FIG. 9 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 9. — Simpson's ratio diagram, comparing the means of the hypodigm sample of MTIII from Perpignan (own data and Samson 1975: table 8) with sample means from Çalta (data own and Eisenmann & Sondaar 1998: table 13) and single specimens from Roussillon and Iarăs-Cariera (data Samson 1975: table 8). Standard (in common logs) and measurements (in mm): 1, length 2.36; 2, proximal breadth 1.63; 3, proximal diameter 1.55; 4, diameter of proximal articular surface 1.50; 5, distal articular breadth 1.58; 6, distal protuberance breadth 1.62; 7, distal keel diameter 1.50; 8, midshaft breadth 1.47.

FIG. 5 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 5. — Simpson's ratio diagram, comparing single MCIII from Le Soler (data Alberdi & Aymar 1995: table 2) with sample means from Polgardi and Baltavar (own data). Standard (in common logs) and measurements (in mm): 1, length 2.29; 2, proximal breadth 1.63; 3, proximal diameter 1.485; 4, diameter of proximal articular surface 1.445; 5, distal articular breadth 1.59; 6, distal protuberance breadth 1.63; 7, keel diameter 1.48; 8, midshaft breadth 1.49.

FIG. 3 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 3. — Simpson's ratio diagram, comparing the means of the hypodigm sample of MTIII from Perpignan (own data and Samson 1975: table 8) with single specimen from Montpellier. Standard (in common logs) and measurements (in mm): 1, length 2.36; 2, proximal breadth 1.63; 3, proximal diameter 1.55; 4, diameter of proximal articular surface 1.50; 5, distal articular breadth 1.58; 6, distal protuberance breadth 1.62; 7, distal keel diameter 1.50; 8, midshaft breadth 1.47.

FIG. 1. — A, left upper M1-2 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 1. — A, left upper M1-2 (Ipswich Borough Council Museum and Galleries R-1876-4.2) of Hipparion sp. of the crassum Group, probably from the Nodule Bed, Suffolk, England. Note strongly plicated enamel, short protocone, and open hypoconal groove; B, right lower p3-4 (IPSMG R-1876-4.11) of Hipparion sp. of the crassum Group, probably from the Nodule Bed, Suffolk, England. Note crenulated enamel and the lack of a protostylid.

FIG. 2 in Latest Hipparion Christol, 1832 in Europe. A review of the Pliocene Hipparion crassum Gervais Group and other finds (Mammalia, Equidae)

FIG. 2. — Simpson's ratio diagram, comparing the means of the hypodigm sample of MTIII from Perpignan (data own and Samson 1975: table 8) with single specimen from Roussillon. Standard (in common logs) and measurements (in mm): 1, length 2.36; 2, proximal breadth 1.63; 3, proximal diameter 1.55; 4, diameter of proximal articular surface 1.50; 5, distal articular breadth 1.58; 6, distal protuberance breadth 1.62; 7, distal keel diameter 1.50; 8, midshaft breadth 1.47.

Figure 11 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 11. Comparative views of the skull and mandible of (A) Neofelis nebulosa, and (B) Paramachairodus ogygia (artwork by M. Antón).

Figure 10 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 10. Photographs of the first to seventh cervical vertebrae (C1-C7) (anterior to left) in Fig. 9, in lateral view. A, Paramachairodus ogygia from Batallones-1. B, Panthera pardus.

Figure 1 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 1. Left mastoid morphology of some species of Felidae showing the different development of the mastoid process (m.p.) and paraoccipital process (p.p.). A, Panthera leo. B, Paramachairodus ogygia from Batallones-1, B-1377. C, Smilodon fatalis from Rancho La Brea. D, B-1377, skull of P. ogygia from Batallones-1 in left lateral view with mastoid area circled.

Figure 4 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 4. Left hemimandibles of Felidae showing differences in the development of the mandibular coronoid process. A, Panthera leo. B, Paramachairodus ogygia from Batallones-1. C, Smilodon fatalis from Rancho La Brea.

Figure 5 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 5. Comparative views of the skull and mandible of two Smilodontini species. A, Paramachairodus ogygia. B, Megantereon cultridens (artwork by M. Antón).

Figure 8 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 8. Composite reconstruction of the skull, mandible and cervical vertebrae of Paramachairodus ogygia, based on material of several individuals from Batallones-1, showing the inferred position of the main cranio-cervical muscles relevant to the canine shear-bite (artwork by M. Antón).

Figure 9 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite

Figure 9. Photographs of first to seventh cervical vertebrae (C1-C7) (anterior to left) in dorsal view. A, Paramachairodus ogygia from Batallones-1, respectively, B-4561, B-5407, B-744 (5), B-5458, B-5459, B-707 (12) and B-707 (12) (the latter have the same number); B, Panthera pardus, 1599.