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10 results for “Caenorhabditis remanei”
FIGURE 3 in Comparison of the cryptic nematode species Caenorhabditis brenneri sp. n. and C. remanei (Nematoda: Rhabditidae) with the stem species pattern of the Caenorhabditis Elegans group
FIGURE 3. Caenorhabditis brenneri sp. n. male. A: posterior end ventral showing bursa, spicules, gubernaculum; note the striped pattern of the cuticle in the posterior part of the tail; B: posterior end lateral; C: spicules and gubernaculum subventral; arrow points to the conspicuous lateral projections on the gubernaculum ("ears"); D: series demonstrating the bending of the gubernaculum when the spicules are extruded, lateral view, also showing the hook; E–F: aberrant right (E) and normal left spicule (F) of the same specimen lateral; G–I: aberrant positions of genital papillae: both GP1 positioned anterior of the bursa (G, H), right GP1shifted to the anterior margin of the bursa (I).
FIGURE 2 in Comparison of the cryptic nematode species Caenorhabditis brenneri sp. n. and C. remanei (Nematoda: Rhabditidae) with the stem species pattern of the Caenorhabditis Elegans group
FIGURE 2. Caenorhabditis brenneri sp. n. female. A: anterior end subventral, with anterior end of lateral canal; B: anterior end ventral; C: pharynx region with lateral field and deirid; D: secretory-excretory system at the level of the deirid ventral; E: anus region lateral, with posterior end of lateral canal and phasmid.
FIGURE 1 in Comparison of the cryptic nematode species Caenorhabditis brenneri sp. n. and C. remanei (Nematoda: Rhabditidae) with the stem species pattern of the Caenorhabditis Elegans group
FIGURE 1. Distribution map for three Caenorhabditis species. Records from west to east: for C. brenneri sp. n. (circles): Costa Rica, Trinidad, Guadeloupe, (? Bukawu), Bangalore, Penang, Sumatra, Bali; for C. remanei (squares) North America (Washington, Ohio, Indiana, New York, Connecticut, Massachusetts), Europe (North-France, Switzerland, Germany, Hungary), East Asia (Shanghai, Kyushu, Honshu); for the recently discovered gonochoristic C. sp. n. 5 in China (triangles): Sanjiang, Guangxi Province (JU727); Guangzhou, Guangdong Province (SB378). Details in text.
FIGURE 5 in Comparison of the cryptic nematode species Caenorhabditis brenneri sp. n. and C. remanei (Nematoda: Rhabditidae) with the stem species pattern of the Caenorhabditis Elegans group
FIGURE 5. Phylogenetic tree (after Kiontke & Sudhaus 2006) and geographic distribution of the Elegans group and related species. With the exception of C. craspedocerca (Völk) and C. perrieri (Maupas), all species were found in Asia. Species highlighted in red are so far only known from Asia. *C. clavopapillata (Kreis & Faust) was isolated from captive dogs and monkeys in the USA. Its natural range is unknown.
FIGURE 4 in Comparison of the cryptic nematode species Caenorhabditis brenneri sp. n. and C. remanei (Nematoda: Rhabditidae) with the stem species pattern of the Caenorhabditis Elegans group
FIGURE 4. Aspects of male copulatory structures in C. brenneri sp. n. (A–D) and C. remanei (E–G). A and E: bursa in ventral view showing precloacal hook, distal part of gubernaculum and genital papillae (GP). In A the GPs are numbered (v = ventral GPs, ad = anterior dorsal GP, pd = posterior dorsal GP slightly out of focus). The differences in size and shape of the bursa in A and E are individual differences and do not mark differences between the species. B: male tail in lateral view. Arrow points to precloacal hook, arrowhead points to distal part of gubernaculum which is bent dorsally in living animals. C and F: cloacal region with precloacal hook and distal part of gubernaculum in situ. D and G: isolated gubernaculum in ventral view and spicules (G). Note that the two lateral processes (ears) are larger and more strongly refractive in C. brenneri sp. n. than in C. remanei. Scale is the same in Figs. A, B, E; and in Figs. C, D, F, G, respectively.
Data from: Experimental evolution: assortative mating and sexual selection, independent of local adaptation, lead to reproductive isolation in the nematode Caenorhabditis remanei
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Evolution of phenotypic plasticity and transgenerational effects of heat stress in the nematode Caenorhabditis remanei
GEO Series GSE62841. Caenorhabditis remanei. 48 samples. Type: Expression profiling by high throughput sequencing.
Dissecting the genetic basis of an evolved acute heat stress and oxidative stress resistance in the nematode Caenorhabditis remanei reveals a complex and unique genetic architecture
GEO Series GSE108235. Caenorhabditis remanei. 28 samples. Type: Expression profiling by high throughput sequencing.
Environmental and evolutionary drivers of the modular gene regulatory network underlying phenotypic plasticity for stress resistance in the nematode Caenorhabditis remanei
GEO Series GSE115496. Caenorhabditis remanei. 48 samples. Type: Expression profiling by high throughput sequencing.
Rapid evolution of phenotypic plasticity and shifting thresholds of genetic assimilation in the nematode Caenorhabditis remanei
GEO Series GSE56510. Caenorhabditis remanei. 36 samples. Type: Expression profiling by high throughput sequencing.
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