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Fig. 4 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 4. Phylogenetic tree of Rodentolepis spp. (Hymenolepididae: Cestoda) based on cox1 mitochondrial DNA. Phylogenetic tree inferred using Bayesian method. Maximum Likelihood bootstrap values of clades are listed first, followed by Bayesian Posterior Probabilities respectively, for clade frequencies exceeding 65%.
Fig. 1 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 1. Morphological features of Rodentolepis microstoma: (A, D, G, J) scolex and rostellar hooks; (B, E, H, K) mature proglottids; (C, F, I, L) egg from different host species, (A–C) Akodon; (D–F) Necromys; (G–I) Thaptomys; (J–L) Oxymycterus.
Fig. 3 in Rodentolepis microstoma isolated from different species of Sigmodontinae rodents (Rodentia: Cricetidae) in the Cuenca del Plata, Argentina: Morphological aspects and molecular characterization
Fig. 3. Phylogenetic tree of Rodentolepis spp. (Hymenolepididae: Cestoda) based on ITS1 mitochondrial DNA. Phylogenetic tree inferred using Bayesian method. Maximum Likelihood bootstrap values of clades are listed first, followed by Bayesian Posterior Probabilities respectively, for clade frequencies exceeding 65%.
Fig. 5 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 5. Maximum likelihood phylogenetic tree of Kontrimavichusia Makarikov & Binkienė, 2022 and Hymenolepis Weinland, 1858 based on analysis of partial sequences of the 28S rRNA gene. Bootstrap support given for maximum likelihood analysis based on 1000 replicates. Bootstrap support values lower than 70% are not shown.
Fig. 4 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 4. Kontrimavichusia hobergi sp. nov. A. Paratype (ISEA AM17-236#1), cirrus and vagina, ventral view. B. Holotype (ISEA AM17-236#3), pregravid proglottis, showing appearance of uterine diverticula, dorsal view. C. Holotype, gravid proglottis, showing labyrinthine uterus, dorsal view. D. Holotype, egg. E. Holotype, embryonic hooks. Abbreviations: al = anterolateral; m = median; pl = postero-lateral. Scale bars: A = 50 µm; B–C = 300 µm; D = 20 µm; E = 10 µm.
Fig. 1 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 1. Kontrimavichusia testiculata sp. nov. A. Holotype (ISEA AM14-134#1), scolex, dorso-ventral view. B. Paratype (ISEA AM14-147#2), scolex, sub-lateral view. C. Paratype (ISEA AM14-142#2), rostellar hooks in profile and frontal view (note narrow hook guard). D. Holotype, male mature proglottides, dorsal view. E. Holotype, hermaphroditic mature proglottis, dorsal view. F. Paratype (ISEA AM14-147#2), genital ducts, dorsal view. Scale bars: A–B, F = 100 µm; C = 10 µm; D–E = 300 µm.
Fig. 6 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 6. Maximum likelihood phylogenetic tree of species of Kontrimavichusia Makarikov & Binkienė, 2022 based on analysis of partial sequences of the nad1 gen. Bootstrap support given for maximum likelihood analysis based on 1000 replicates. Bootstrap support values lower than 70% are not shown.
Fig. 3 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 3. Kontrimavichusia hobergi sp. nov. A. Paratype (ISEA AM17-242), scolex, dorso-ventral view. B. Paratype (ISEA AM1 17-243#3), scolex, sub-lateral view. C. Holotype (ISEA AM17-236#3) (left) and paratype (ISEA AM 17-236#2) (centre, right), rostellar hooks in profile and frontal view (note narrow hook guard). D. Holotype, male mature proglottides, dorsal view. E. Holotype, hermaphroditic mature proglottis, dorsal view. F. Holotype, genital ducts, dorsal view. Scale bars: A–B, F = 100 µm; C = 10 µm; D–E = 300 µm.
Fig. 2 in New species of Kontrimavichusia Makarikov & Binkienė, 2022 (Eucestoda: Hymenolepididae) from arvicoline rodents (Rodentia: Cricetidae) from the North Caucasus
Fig. 2. Kontrimavichusia testiculata sp. nov. A. Paratype (ISEA AM14-147#2), cirrus and vagina, ventral view. B. Holotype (ISEA AM14-134#1), pregravid proglottis, showing appearance of uterine diverticula, dorsal view. C. Holotype, gravid proglottis, showing labyrinthine uterus, dorsal view. D. Holotype, egg. E. Holotype, embryonic hooks. Abbreviations: al = anterolateral; m = median; pl = postero-lateral. Scale bars: A = 50 µm; B–C = 300 µm; D = 20 µm; E = 10 µm.
TABLE 1 in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>TABLE 1 <b>Character State of the Carotid Circulatory Pattern in Species-group Taxa of <i>Oecomys</i></b> (Arranged alphabetically by valid species and chronologically by attributed synonyms.)</p><table><thead><tr><th>Species-group Taxa Type Localities</th><th></th></tr><tr><th colspan="2">(Holotypes) Complete a Derived b</th></tr></thead><tbody><tr><th><i>O. auyentepui</i> Tate, 1939 Mt. Auyan-tepui, Venezuela (AMNH 131156)</th><td>+</td></tr><tr><th><i>O. bicolor</i> (Tomes, 1860) Gualaquiza, Ecuador (BMNH 7.1.1.96)</th><td>+</td></tr><tr><th><i>dryas</i> Thomas, 1900 Paramba, Ecuador (BMNH 1899.12.5.4)</th><td>+</td></tr><tr><th><i>benevolens</i> Thomas, 1901 Chimate, Bolivia (BMNH 1.2.1.14)</th><td>+</td></tr><tr><th><i>rosilla</i> Thomas, 1904 La Union, Venezuela (BMNH 1904.5.7.37)</th><td>+</td></tr><tr><th><i>nitedulus</i> Thomas, 1910 Essequibo River, Guyana (BMNH 1906.4.8.31)</th><td>+</td></tr><tr><th><i>florenciae</i> Allen, 1916 Florencia, Colombia AMNH 33863</th><td>+</td></tr><tr><th><i>milleri</i> Allen, 1916 Barão de Malgaço, Brazil (AMNH 37117)</th><td>+</td></tr><tr><th><i>trabeatus</i> Allen and Barbour, 1923 Río Jesusito, Panama (MCZ 19837)</th><td>+</td></tr><tr><th><i>endersi</i> Goldman, 1933 Barro Colorado Island, Panama (UMMZ 64931)</th><td>+</td></tr><tr><th><i>phelpsi</i> Tate, 1939c Mt. Auyan-Tepui, Venezuela (AMNH 131164)</th><td>+</td></tr><tr><th><i>occidentalis</i> Hershkovitz, 1960 Paramba, Ecuador (BMNH 1899.12.5.4)</th><td>+</td></tr><tr><th><i>O. catherinae</i> Thomas, 1909 Joinville, Brazil (BMNH 9.11.19.24)</th><td>+</td></tr><tr><th><i>O. cleberi</i> Locks, 1981 Fazenda Água Limpa, Brazil (MN 24131)</th><td>+</td></tr><tr><th>(Holotypes)</th><td>Complete a Derived b</td></tr><tr><th><i>O. concolor</i> (Wagner, 1845) Mouth of Rio Curicuriare, Brazil (NMW B482)</th><td>+</td></tr><tr><th><i>marmosurus</i> Thomas, 1899 Maipures, Colombia (BMNH 1899.9.11.38)</th><td>+</td></tr><tr><th><i>O. flavicans</i> (Thomas, 1894) Mérida, Venezuela (BMNH 1894.9.25.14)</th><td>+</td></tr><tr><th><i>illectus</i> Bangs, 1898 Pueblo Viejo, Colombia (MCZ 8101)</th><td>+</td></tr><tr><th><i>mincae</i> Allen, 1913 Minca, Colombia (AMNH 15332)</th><td>+</td></tr><tr><th><i>O. mamorae</i> (Thomas, 1906b) Mosetenes, Bolivia (BMNH 1900.8.3.21)</th><td>+</td></tr><tr><th><i>O. paricola</i> (Thomas, 1904) Igarapé Assu, Brazil (BMNH 1904.7.4.63)</th><td>+</td></tr><tr><th><i>O. phaeotis</i> Thomas, 1901 Sagrario, Peru (BMNH 1901.1.1.23)</th><td>+</td></tr><tr><th><i>O. rex</i> Thomas, 1910 Supenaam River, Guyana (BMNH 1910.9.29.17)</th><td>+</td></tr><tr><th><i>O. roberti</i> (Thomas, 1904) Santa Anna da Chapada, Brazil (BMNH 1903.7.7.67)</th><td>+</td></tr><tr><th><i>tapajinus</i> Thomas, 1909 Santa Rosa, Brazil (BMNH 1909.3.9.9)</th><td>+</td></tr><tr><th><i>guianae</i> Thomas, 1910 Supenaam River, Guyana (BMNH 1910.5.4.23)</th><td>+</td></tr><tr><th><i>O. rutilus</i> Anthony, 1921 Kartabo, Guyana (AMNH 42910)</th><td>+</td></tr><tr><th><i>O. speciosus</i> (Allen and Chapman, 1893) Princes Town, Trinidad (AMNH 5942/4672)</th><td>+</td></tr><tr><th>(Holotypes)</th><td>Complete a Derived b</td></tr><tr><th><i>trichurus</i> Allen, 1899 El Libano, Colombia (AMNH 15328)</th><td>+</td></tr><tr><th><i>caicarae</i> Allen, 1913 Caicara, Venezuela (AMNH 29875)</th><td>+</td></tr><tr><th><i>O. superans</i> Thomas, 1911 Canelos, Ecuador (BMNH 1911.7.19.12)</th><td>+</td></tr><tr><th><i>palmeri</i> Thomas, 1911 Canelos, Ecuador (BMNH 1911.7.19.13)</th><td>+</td></tr><tr><th><i>melleus</i> Anthony, 1924 Zamora, Ecuador (AMNH 36560)</th><td>+</td></tr><tr><th><i>O. trinitatis</i> (Allen and Chapman, 1893) Princes Town, Trinidad (AMNH 5943/4673)</th><td>+</td></tr><tr><th><i>subluteus</i> Thomas, 1898 Cundinamarca, Colombia (BMNH 1898.7.3.2)</th><td>+</td></tr><tr><th><i>fulviventer</i> Allen, 1899 Quebrada Seca, Venezuela (AMNH 14735)</th><td>+</td></tr><tr><th><i>palmarius</i> Allen, 1899 Quebrada Seca, Venezuela (AMNH 14733)</th><td>+</td></tr><tr><th><i>tectus</i> Thomas, 1901 Bugaba, Panama (BMNH 1900.7.11.43)</th><td>+</td></tr><tr><th><i>klagesi</i> Allen, 1904 El Yagual, Venezuela (AMNH 16966)</th><td>+</td></tr><tr><th><i>frontalis</i> Goldman, 1912 Corazal, Panama (USNM 171531)</th><td>+</td></tr><tr><th><i>helvolus</i> Allen, 1913 Villavicencio, Colombia (AMNH 34578)</th><td>+</td></tr><tr><th><i>vicencianus</i> Allen, 1913 Villavicencio, Colombia (AMNH 34584)</th><td>+</td></tr><tr><th>Species-group Taxa</th><td></td></tr><tr><th>Type Localities</th><td></td></tr><tr><th>(Holotypes)</th><td>Complete a Derived b</td></tr><tr><th><i>osgoodi</i> Thomas, 1924</th><td>+</td></tr><tr><th>Moyobamba, Peru</th><td></td></tr><tr><th>(BMNH 1924.7.11.16)</th><td></td></tr><tr><th><i>splendens</i> Hayman, 1938</th><td>+</td></tr><tr><th>Mayaro, Trinidad</th><td></td></tr><tr><th>(BMNH 1937.11.11.2)</th><td></td></tr></tbody></table><p><sup>a</sup> Complete: supraorbital and infraorbital branches of the stapedial artery form major blood supply to the orbitofacial region; sphenofrontal and stapedial foramina present; vascular grooves cross both the inner surface of the squamosal and alisphenoid bones and the posterolateral corner of the parapterygoid fossa; posterior opening to alisphenoid canal large.</p><p><sup>b</sup> Derived: supraorbital and infraorbital branches absent, distal orbitofacial circulation arising from secondary anastomosis to the internal carotid; sphenofrontal foramen absent, stapedial foramen absent or minute; no vascular grooves found on the inner surface of the squamosal and alisphenoid bones or on the posterolateral corner of the parapterygoid fossa; posterior opening to alisphenoid canal irregularly formed or occluded; secondary osseous groove internally crosses the roof of the parapterygoid fossa.</p><p><sup>c</sup> Based on the type as restricted by Musser and Patton (1989).</p>
TABLE 7 in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>TABLE 7 <b>External and Craniodental Measurements (in mm) of the Type Specimens of <i>Hesperomys concolor</i> Wagner, <i>Rhipidomys marmosurus</i> Thomas, and <i>Oryzomys mamorae</i> Thomas</b></p><table><thead><tr><th></th><th><i>concolor</i></th><th><i>marmosurus</i> a</th><th><i>mamorae</i> b</th></tr></thead><tbody><tr><th>Variable</th><td>NMW B482</td><td>BMNH 1899.9.11.38</td><td>BMNH 1900.8.3.21</td></tr><tr><th>HBL</th><td>—</td><td>124</td><td>130</td></tr><tr><th>TL</th><td>—</td><td>157</td><td>168</td></tr><tr><th>HFL</th><td>—</td><td>26 (28)</td><td>27</td></tr><tr><th>EL</th><td>—</td><td>18</td><td>20</td></tr><tr><th>ONL</th><td>29.2</td><td>33.8</td><td>33.1</td></tr><tr><th>ZB</th><td>15.9</td><td>—</td><td>17.5</td></tr><tr><th>BBC</th><td>13.3</td><td>12.6</td><td>12.6</td></tr><tr><th>DBC</th><td>—</td><td>9.1</td><td>9.2</td></tr><tr><th>IOB</th><td>5.0</td><td>5.8</td><td>5.1</td></tr><tr><th>BOC</th><td>—</td><td>6.9</td><td>7.3</td></tr><tr><th>LR</th><td>7.7</td><td>9.4</td><td>8.9</td></tr><tr><th>BR</th><td>5.7</td><td>6.2</td><td>4.8</td></tr><tr><th>PPL</th><td>—</td><td>11.3</td><td>10.8</td></tr><tr><th>BPL</th><td>6.0</td><td>6.6</td><td>6.2</td></tr><tr><th>LIF</th><td>4.8</td><td>5.4</td><td>5.9</td></tr><tr><th>BIF</th><td>2.4</td><td>2.5</td><td>2.7</td></tr><tr><th>LD</th><td>7.4</td><td>8.2</td><td>7.9</td></tr><tr><th>BBP</th><td>5.8</td><td>6.3</td><td>6.4</td></tr><tr><th>BZP</th><td>2.9</td><td>3.7</td><td>3.4</td></tr><tr><th>CLM</th><td>4.8</td><td>4.9</td><td>5.2</td></tr><tr><th>WM1</th><td>1.3</td><td>1.3</td><td>1.5</td></tr></tbody></table><p><sup>a</sup> External data as given by Thomas (1899).</p><p><sup>b</sup> External data as given by Thomas (1906b).</p>
Linked collectors and determiners for: Revision of Neacomys spinosus (Thomas, 1882) (Rodentia: Cricetidae) with emphasis on Peruvian populations and the description of a new species.
Natural history specimen data linked to collectors and determiners held within, "Revision of Neacomys spinosus (Thomas, 1882) (Rodentia: Cricetidae) with emphasis on Peruvian populations and the description of a new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/893e07da-8ed6-4e9d-ba47-44b13bb49b65">https://bionomia.net/dataset/893e07da-8ed6-4e9d-ba47-44b13bb49b65</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/893e07da-8ed6-4e9d-ba47-44b13bb49b65">https://gbif.org/dataset/893e07da-8ed6-4e9d-ba47-44b13bb49b65</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Reevaluation of Rhipidomys emiliae (J. A. Allen 1916) and description of a new Rhipidomys (Rodentia: Cricetidae) species from Amazonia and Cerrado.
Natural history specimen data linked to collectors and determiners held within, "Reevaluation of Rhipidomys emiliae (J. A. Allen 1916) and description of a new Rhipidomys (Rodentia: Cricetidae) species from Amazonia and Cerrado". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/2b2e056e-f17a-4e90-ba94-74450e15f891">https://bionomia.net/dataset/2b2e056e-f17a-4e90-ba94-74450e15f891</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/2b2e056e-f17a-4e90-ba94-74450e15f891">https://gbif.org/dataset/2b2e056e-f17a-4e90-ba94-74450e15f891</a>. Formatted as a Frictionless Data package.
Fig. 2 in Peromyscus boylii (Rodentia: Cricetidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult male Peromyscus boylii boylii (Museum of Vertebrate Zoology [MVZ] 156578) from Hopland Field Station, Mendocino County, California (30u009N, 123u059W). Greatest length of skull is 27.3 mm. Photograph by Matina C. Kalcounis- Rueppell.
Fig. 3 in Peromyscus boylii (Rodentia: Cricetidae)
Fig. 3.—Geographic distribution of Peromyscus boylii. Subspecies are: 1, P. b. boylii; 2, P. b. glasselli; 3, P. b. rowleyi; 4, P. b. utahensis. Map redrawn from Carleton (1989) and Bradley and Schmidly (1999) with modifications from Hoffmeister (1986), Cockrum (1982), and Cockrum (1960) for Arizona; Stephens (1906), Jameson and Peeters (1988), and Grinnell (1933) for California; Armstrong (1972), Warren (1910), and Svoboda et al. (1988) for Colorado; Hall (1946) for Nevada; Bailey (1931) and Findley et al. (1975) for New Mexico; Caire et al. (1989) for Oklahoma; Verts and Carraway (1998) and Grinnell (1933) for Oregon; Davis and Schmidly (1994) and Schmidly (1977) for Texas; Durrant (1946), Barnes (1927), and Durrant (1952) for Utah; and Tiemann-Boege et al. (2000) for Mexico. The position of San Pedro Nolasco Island, Gulf of California, Sonora, Mexico (27u589N, 111u249W) is approximate.
Fig. 1 in Peromyscus boylii (Rodentia: Cricetidae)
Fig. 1.—An adult male Peromyscus boylii rowleyi from lower Robertson Creek at the Hastings Natural History Reserve, Monterey County, California (22.5 km southeast of Carmel Valley, 36u229N, 121u229W). Photograph by Matina C. Kalcounis-Rueppell, 27 July 2002.
Fig. 4 in Loxodontomys micropus (Rodentia: Cricetidae)
Fig. 4.—One of the habitat types occupied by Loxodontomys micropus; dense Nothofagus underbrush where L. micropus reaches high densities in western Santa Cruz Province, Argentina (Río Ñires; in the background Cerro Punta de Vacas).
Fig. 2 in Loxodontomys micropus (Rodentia: Cricetidae)
Fig. 2.—Dorsal, ventral, and lateral views of the skull and lateral view of the mandible of adult male Loxodontomys micropus from Estancia La Ensenada, Santa Cruz, Argentina (Colección de Mamíferos del Centro Nacional Patago´nico [CNP] 536). Condyloincisive length 5 31.5 mm.
Fig. 3 in Loxodontomys micropus (Rodentia: Cricetidae)
Fig. 3.—Geographic distribution of Loxodontomys micropus based on compiled localities from several sources and museum collections. Diffuse gray area indicates uncertain limits; gray points indicate isolated populations recorded in central Patagonia.
Fig. 1 in Loxodontomys micropus (Rodentia: Cricetidae)
Fig. 1.—An adult male Loxodontomys micropus from El Maitén, northwestern Chubut Province, Argentina.
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Allen Brain Atlas
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