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FIG. 6 in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 6. Habitat of Neacomys marajoara at Tauari Farm, municipality of Chaves, Marajó Island, state of Pará, Brazil. Photo by Rogério V. Rossi.

FIG. 12 in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 12. Dorsal, ventral, lateral cranial views and lateral view of mandible of Neacomys xingu (UFMT 1268, holotype).

FIG. 3 in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 3. Scatter plots of PC1 (horizontal axis) and PC2 (vertical axis) for pairwise analyses of craniodental measurement data for species in the Dubosti Group of Neacomys. In each plot, species are represented by minimum convex polygons that enclose all points in the plane of PC1 and PC2. A, N. dubosti (dub) versus N. marajoara (mar); B, N. dubosti versus N. vossi (vos); C, N. dubosti versus N. xingu (xin); D, N. marajoara versus N. vossi; E, N. marajoara versus N. xingu; F, N. vossi versus N. xingu.

FIG. 7 in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 7. Dorsal, ventral, and lateral cranial views and lateral view of mandible of Neacomys marajoara (MPEG 40432, holotype).

FIG. 5 in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 5. Collection localities of specimens of the Dubosti Group of Neacomys examined in the present study. Numbers are keyed to entries in our gazetteer (appendix 1).

FIG. 2 A–C in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 2 A–C (above and following two pages). Bayesian phylogeny of Neacomys based on cytochrome b sequence data. Numbers represent Bayesian posterior probabilities (above) and ML bootstrap support (below) at nodes recovered by both analyses (bootstrap support for nodes only recovered by our ML analysis are shown in appendix 2). Only ML bootstrap support>50% is shown. Branch tips are labeled with geographic identifiers and voucher codes listed in table 1. Specimens marked with asterisks (*) indicate holotypes.

FIG. 1 in Systematics of Neotropical Spiny Mice, Genus Neacomys Thomas, 1900 (Rodentia: Cricetidae), from Southeastern Amazonia, with Descriptions of Three New Species

FIG. 1. SEM images of molar toothwear age classes of Neacomys amoenus used in this study (based on Voss, 1991). From left to right: age class 1 (UFMT 4050), age class 2 (UFMT 1758), age class 3 (UFMT 1760), age class 4 (UFMT 1759), and age class 5 (UFMT 915). Arrows indicate the incompletely erupted M3 in age class 1, the distinct M2 anteroloph (not fused with the paracone) in age class 3, and the obliterated M2 anteroloph (fused with the paracone) in age class 4.

opencc-by-4.0Sep 2003View details →

Fig. 9 in Three new species of Hyphessobrycon (Characiformes: Characidae) from the upper rio Araguaia basin in Brazil

Fig. 9. Hyphessobrycon weitzmanorum, holotype, MZUSP 73315, 22.1 mm SL, Brazil, Mato Grosso, município de Alto Araguaia, córrego Mosquito.

Fig. 8 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 8. Phanacis urhani sp. nov., ♀. a. Mesosoma in lateral view. b. Mesopleuron. c. Mesosoma in posterior view. d. Antenna. e. Leg. f. Radial cell of forewing.

Fig. 4 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 4. Phanacis ciceki sp. nov., ♀. a. Head in anterior view. b. Mesosoma in dorsal view. c. Metasoma in lateral view. d. Pronotum in dorsal view. e. Scutum in dorsal view. f. Scutellum in dorsal view.

Fig. 5 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 5. Phanacis ciceki sp. nov., ♀. a. Antenna. b. Head in dorsal view. c. Radial cell of forewing. d. Mesosoma in lateral view. e. Mesopleuron. f. Scutellum in lateral view.

Fig. 1 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 1. Aulacidea turguti sp. nov., ♀. a. Head in anterior view. b. Mesosoma in dorsal view. c. Metasoma in lateral view. d. Head in posterior view. e. Scutum in dorsal view. f. Scutellum in dorsal view.

Fig. 7 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 7. Phanacis urhani sp. nov., ♀. a. Head in anterior view. b. Mesosoma in dorsal view. c. Metasoma in lateral view. d. Head in dorsal view. e. Scutum in dorsal view. f. Scutellum in dorsal view.

Fig. 2 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 2. Aulacidea turguti sp. nov., ♀. a. Mesosoma in lateral view. b. Mesosoma in posterior view. c. Metasomal tergites T2, T3 and T4. d. Antenna. e. Leg. f. Radial cell of forewing.

Fig. 9 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey

Fig. 9. Phanacis urhani sp. nov., mature gall on host plant, Cirsium vulgare (Savi) Ten. (photos by M. Azmaz).

opencc-by-4.0Jun 2021View details →

Three-Dimensional Hydrodynamic Simulations of Convective Nuclear Burning In Massive Stars Near Iron Core Collapse

<p>Data products from ApJ article Three-Dimensional Hydrodynamic Simulations of Convective Nuclear Burning In Massive Stars Near Iron Core Collapse, 2021. Four 3D core-collapse supernova progenitor models. Works that utilize these progenitor models are required to cite article. The models were evolved to times listed in Table 1 of the article, the collapse time according to the 1D MESA model. All 3D data are in FLASH4 format using the HDF5 data structure. </p>

opencc-by-4.0Dec 2014View details →

PLATE IA. Natula Gorochov, 1987. (A–L), Natula matsuurai (Sugimoto, 2001): A, Male; B, Female; C, Face with a transverse dark strip near epistomal suture; D, Fifth joint of maxillary palpi hatchet shaped; E, Lateral field of tegmina deeper than lateral lobe of pronotum; F, Hind tibia with 3 pairs of dorsal spines on both sides but largest inner apical spurs as long as or half of basitarsus; G, Fore tibia with oval shaped outer and inner tympanum; H, Harp vein only one, Mirror area occupying half dorsal surface, not divided with a small concentric inner veinlet; I, Pronotum with roundly convex anterior margin; J, Female ovipositor strongly upcurved, half as long as hind femur, three fifth area from base widened and bumpy, with a dorsal groove, cerci as long as ovipositor; K, Male sub-genital plate longer than wide, hind margin narrowly truncated with a small projected median lobe, two styli present; L, Female sub-genital plate roundly triangular. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.

PLATE IA. Natula Gorochov, 1987. (A–L), Natula matsuurai (Sugimoto, 2001): A, Male; B, Female; C, Face with a transverse dark strip near epistomal suture; D, Fifth joint of maxillary palpi hatchet shaped; E, Lateral field of tegmina deeper than lateral lobe of pronotum; F, Hind tibia with 3 pairs of dorsal spines on both sides but largest inner apical spurs as long as or half of basitarsus; G, Fore tibia with oval shaped outer and inner tympanum; H, Harp vein only one, Mirror area occupying half dorsal surface, not divided with a small concentric inner veinlet; I, Pronotum with roundly convex anterior margin; J, Female ovipositor strongly upcurved, half as long as hind femur, three fifth area from base widened and bumpy, with a dorsal groove, cerci as long as ovipositor; K, Male sub-genital plate longer than wide, hind margin narrowly truncated with a small projected median lobe, two styli present; L, Female sub-genital plate roundly triangular.

Armature formula of P1–P4 as follows: P5 (Fig. 2B). With outer seta of BENP arising from long setophore. Endopodal lobe triangular, reaching middle of exopod; with small spinules along outer margin and at base of inner setae; with five elements – one outer subdistal, one apical and one inner subdistal normal seta, and two inner bifurcate elements. Exopod elongate, 2.8 times as long as wide; with spinules along inner margin and with few proximal outer spinules; with six elements – three outer slender, short setae, two apical elements, of which outermost one shorter, and one inner seta. in Proposal of new genera and species of the subfamily Diosaccinae (Copepoda: Harpacticoida: Miraciidae)

Armature formula of P1–P4 as follows: P5 (Fig. 2B). With outer seta of BENP arising from long setophore. Endopodal lobe triangular, reaching middle of exopod; with small spinules along outer margin and at base of inner setae; with five elements – one outer subdistal, one apical and one inner subdistal normal seta, and two inner bifurcate elements. Exopod elongate, 2.8 times as long as wide; with spinules along inner margin and with few proximal outer spinules; with six elements – three outer slender, short setae, two apical elements, of which outermost one shorter, and one inner seta.

Absolute model ages of three craters in the vicinity of the Chang'E-5 landing site and their geologic implications

<p>We used the Crater Size Frequency distribution (CSFD) method to yield the formation ages of Pythagora, Sharp B, and Harpalus crater, and the crater density values (N(1)). Here we provide the crater counting data.</p>