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1,039 results for “1898”
FIG. 13 in Octocorals (Cnidaria, Anthozoa) from Reunion, with a description of two new species of the genus Sinularia May, 1898 and notes on the occurrence of other species
FIG. 13. — Live colonies of: A, B, Lobophytum depressum Tixier-Durivault, 1966; A, with extended polyps; B, with retracted polyps; C, D, Lobophytum latilobatum Verseveldt, 1971; C, with extended polyps; D, with retracted polyps; E, Lobophytum pauciflorum (Ehrenberg, 1834); F, Rhytisma fulvum fulvum (Forskål, 1775).
FIG. 15 in Octocorals (Cnidaria, Anthozoa) from Reunion, with a description of two new species of the genus Sinularia May, 1898 and notes on the occurrence of other species
FIG. 15. — Live colonies of: A, Sinularia brassica May, 1898; B, Sinularia densa Whitelegge, 1897; C, Sinularia erecta Tixier-Durivault, 1945; D, Sinularia gibberosa Tixier-Durivault, 1970; E, Sinularia hirta (Pratt, 1903); F, Sinularia molesta Tixier-Durivault, 1970.
FIG. 8. — Sinularia tessieri n in Octocorals (Cnidaria, Anthozoa) from Reunion, with a description of two new species of the genus Sinularia May, 1898 and notes on the occurrence of other species
FIG. 8. — Sinularia tessieri n. sp.: A, holotype (ZMTAU Co 34502); B, paratype (RMNH Coel 40120). Scale bar: 10 mm.
FIG. 3 in Octocorals (Cnidaria, Anthozoa) from Reunion, with a description of two new species of the genus Sinularia May, 1898 and notes on the occurrence of other species
FIG. 3. — Sarcophyton subviride Tixier-Durivault, 1958 (ZMTAU Co 34408): A, scale- and rod sclerites of tentacle; B, point sclerites of polyp; C, D, sclerites of polyparium; C, clubs of surface layer; D, tubercular spindles of interior. Scale bars: 0.10 mm.
Figures 28–31. Eucereon latifascia sensu Hampson, 1898. 28–29 in A preliminary catalogue of the moths (Lepidoptera except Papilionoidea) of Tobago, West Indies
Figures 28–31. Eucereon latifascia sensu Hampson, 1898. 28–29, ♂ Morne Bleu, Textel Installation, at light, 11 Oct 1978 (M.J.W. Cock) [MJWC]. 30–31, ♀ Parrylands Oilfield, MVL, 25 Jul 1981 (M.J.W. Cock) [MJWC].
Fig. 1 in Primer registro de Celidophylla albimacula Saussure y Pictet, 1898 (Orthoptera: Tettigoniidae) en Panamá
Fig. 1. Vista del ejemplar vivo de Celidophylla albimacula Saussure y Pictet, 1898 (Orthoptera: Tettigoniidae).
Figure 4 in Ultrastructural redescription of Chordodes moraisi (Carvalho, 1942) and Chordodes straviarskii Carvalho and Feio, 1950, and re-interpretation of Chordodes gestri Camerano, 1904 and Pseudochordodes griffinii (Camerano, 1898) (Gordiida, Nematomorpha)
Figure 4. SEM of male of ''Pseudochordodes griffinii'' holotype. (A) Cuticle of midbody; (B) areolar group in the middle region of the body. Scale bars: 10 mm.
Figure 2 in Ultrastructural redescription of Chordodes moraisi (Carvalho, 1942) and Chordodes straviarskii Carvalho and Feio, 1950, and re-interpretation of Chordodes gestri Camerano, 1904 and Pseudochordodes griffinii (Camerano, 1898) (Gordiida, Nematomorpha)
Figure 2. SEM of female of Chordodes staviarskii holotype. (A) Ventral view of posterior end with cloacal opening, bristles and radiating grooves (arrow). (B, C) Midbody cuticle: (B) areoles types 1–3 and interareolar tubercle; (C) areoles of type 1–3 and clusters containing types 4 and 6. (D) Areoles type 5 and 6 in the longitudinal ventral groove; b, bristles; t, tubercle. Scale bars: 100 mm (A, D); 10 mm (B); 50 mm (C).
Figure 1 in Ultrastructural redescription of Chordodes moraisi (Carvalho, 1942) and Chordodes straviarskii Carvalho and Feio, 1950, and re-interpretation of Chordodes gestri Camerano, 1904 and Pseudochordodes griffinii (Camerano, 1898) (Gordiida, Nematomorpha)
Figure 1. SEM of female of Chordodes moraisi, holotype. (A) Ventral view of posterior end with cloacal opening; (B) midbody cuticle, areoles types 1–3; (C) tubercle in the interareolar furrow; (D, E) areoles type 4 with long filaments in the longitudinal ventral groove. Scale bars: 100 mm (A, E); 50 mm (B–D).
Figure 3 in Ultrastructural redescription of Chordodes moraisi (Carvalho, 1942) and Chordodes straviarskii Carvalho and Feio, 1950, and re-interpretation of Chordodes gestri Camerano, 1904 and Pseudochordodes griffinii (Camerano, 1898) (Gordiida, Nematomorpha)
Figure 3. SEM of male of ''Chordodes gestri'' holotype. (A, B) Ventral view of posterior end: (A) whole posterior end with cloacal opening (arrow); (B) cloacal opening with circumcloacal bristles. (C) Cuticle at the midbody with megareolar pattern. (D) Areolar pattern in the anterior region of the body. Scale bars: 100 mm (A); 50 mm (B); 10 mm (C, D).
Fig. 6. Gunboat Siboga, 1898 in History of collection and discovery of polychaetes (Annelida), including a bibliography, from the Indo-Malay-Philippines Archipelago and surrounding seas
Fig. 6. Gunboat Siboga, 1898. Bijzondere Collecties van de Universiteit van Amsterdam, as reproduced on Wikipedia.
FIGURE 11. Urophonius granulatus Pocock, 1898, dextral pedipalp chela. A, D, E in Systematic Revision of the granulatus Group of Urophonius Pocock, 1893 (Scorpiones, Bothriuridae), with Description of a New Species from Central Chile
FIGURE 11. Urophonius granulatus Pocock, 1898, dextral pedipalp chela. A, D, E. ♂ (MACN). B, C. ♀ (LBRE). A. Dorsal aspect. B. External aspect. C, D. Ventral aspect. F.
Fig. 2 in Scientific Note Radiotelemetry of a female jaú, Zungaro jahu (Ihering, 1898) (Siluriformes: Pimelodidae), passed upstream of Funil Dam, rio Grande, Brazil
Fig. 2. Movements of jaú in Funil Reservoir, rio Grande, and rainfall in rio das Mortes. The y-axis on the left shows distances to Funil Dam. The horizontal dashed line indicates the location of the rio das Mortes mouth before it was flooded.
Fig. 1 in Scientific Note Radiotelemetry of a female jaú, Zungaro jahu (Ihering, 1898) (Siluriformes: Pimelodidae), passed upstream of Funil Dam, rio Grande, Brazil
Fig. 1. Map of Funil Reservoir showing locations (%) of the tagged jaú. Location numbers as in Table 1.
Figure 1 in Evolutionary systematics of the Indian mouse Mus famulus Bonhote, 1898: molecular (DNA/DNA hybridization and 12S rRNA sequences) and morphological evidence
Figure 1. Phylogenetic trees derived from the DNA/DNA hybridization analysis. A and B: Consensus trees resulting from the bootstrap analysis of delta-Tm (A) and delta-mode (B) 12*12 matrices. BP values are indicated when different from 100%. The lengths of the branches correspond to one tree arbitrarily selected among those of the consensus. C and D: Average consensus trees resulting from the weighted jacknife procedure for delta-Tm (C) and delta-mode (D) 13*13 matrices. The thin lines represent nodes that were not present in maximum and minimum consensus trees or that are not supported for all combinations of single deletion analysis. uUnlabelled taxa. The names in bold indicate the differences that can be observed between the two distance estimators (Tm, Mode).
Figure 4 in Evolutionary systematics of the Indian mouse Mus famulus Bonhote, 1898: molecular (DNA/DNA hybridization and 12S rRNA sequences) and morphological evidence
Figure 4. Fifty per cent majority rule consensus of 52 trees derived from the morphological analysis. Each mostparsimonious tree is 54 steps long, and has a Consistency Index of 0.52, a Retention Index of 0.72, and a Rescaled Consistency Index of 0.37. Values given below the branches represent the percentage of trees containing the specified clades.
Figure 3. Synthetic tree derived from the 12S in Evolutionary systematics of the Indian mouse Mus famulus Bonhote, 1898: molecular (DNA/DNA hybridization and 12S rRNA sequences) and morphological evidence
Figure 3. Synthetic tree derived from the 12S rRNA datasets with the inclusion of all substitutions (TV + TI). The thin lines indicate nodes that are not robustly supported by all kinds of analysis. The robustness of the different nodes are indicated as follows: [BP(BPweighted analysis)/BSI (Parsimony)]/[BP(NJ)/Reliability Percentage (ML)].
Fig. 1. Data labels. A. Centris debilis Dominique, 1898 in The primary types of some species of Centris bees described by European entomologists in the 18 and 20 centuries (Hymenoptera: Apidae)
Fig. 1. Data labels. A. Centris debilis Dominique, 1898 (lectotype ♂). B. Centris dominiquella Dominique, 1898 (lectotype ♀).
Fig 2. Data labels. A. Centris zonalis Dominique, 1898 in The primary types of some species of Centris bees described by European entomologists in the 18 and 20 centuries (Hymenoptera: Apidae)
Fig 2. Data labels. A. Centris zonalis Dominique, 1898 (lectotype ♀). B. Centris lyngbyei Jensen- Haarup, 1908 (lectotype ♂).
Fig. 11. Pelodera cylindrica Cobb, 1898 in Comparative and cladistic analyses of the species of the genus Pelodera Schneider, 1866 (Rhabditidae: Nematoda) belonging to the coarctata group
Fig. 11. Pelodera cylindrica Cobb, 1898, female (AMU/ZD/NC slide no. Pelodera cylindrica/HL/AL/ ST/SM/1–10). A–B. En face view (scanning electron microscopy). C–E. Anterior end. F–G. Anterior pharyngeal region. H–I. Posterior pharyngeal region. J. Distal end of anterior and posterior genital branches. K. Vulval region (scanning electron microscopy). L. Uterine region. M–O. Tail end. Scale bars = 10 μm.
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Allen Brain Atlas
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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.