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58 results for “Radix”
Fig. 3a-j in Physico-chemical characteristics of habitats colonized by the pond snail Radix labiata (Gastropoda, Basommatophora, Lymnaeidae): a model approach
Fig. 3a-j: Graphical presentation of essential parameters associated with logistic regression: white vertical line: position of the maximum probability of occurrence (xmax), black bar: optimum range of the given variable, grey-shaded area: range of the given variable that is still tolerated by the species; a) water temperature, b) pH, c) electric conductivity, d) oxygen content in the water, e) nitrate concentration in the water, f) water depth, g) biological oxygen demand within five days, h) content of ammonium nitrogen, i) geographic altitude, j) current velocity.
Fig. 1 in Physico-chemical characteristics of habitats colonized by the pond snail Radix labiata (Gastropoda, Basommatophora, Lymnaeidae): a model approach
Fig. 1: General habitus of the shell of R. labiata as well as the living animal: a) Front view of the shell (height: 1.4 cm, width: 0.75 cm), b) back view of the shell, c) living animal with its typical triangular tentacles.
Fig. 2a-j in Physico-chemical characteristics of habitats colonized by the pond snail Radix labiata (Gastropoda, Basommatophora, Lymnaeidae): a model approach
Fig. 2a-j: Results of the logistic regression procedure carried out for ten environmental variables: a) water temperature, b) pH, c) electric conductivity, d) oxygen content in the water, e) nitrate concentration in the water, f) water depth, g) biological oxygen demand within five days, h) content of ammonium nitrogen, i) geographic altitude, j) current velocity.
Fig. 3 in Radix Rufescens (J. E. Gray, 1822) (Gastropoda: Lymnaeidae), A New Species For Oman And Arabian Peninsula
Fig. 3. Reproductive organs of Radix rufescens: A = ventrally, B–C = praeputium and phallotheca (ag – albuminoid gland, cp – corpus pyriformis, hg – haermaphrodite gland, ng – nidamental gland, ph – phallotheca (penis sheath), pr – prostate, prae – praeputium, ut – uterus, v – vagina, vd – vas deferens). Scale bar: 1 mm
Fig. 4 in Radix Rufescens (J. E. Gray, 1822) (Gastropoda: Lymnaeidae), A New Species For Oman And Arabian Peninsula
Fig. 4. Maximum likelihood tree computed for COI; bootstrap supports/Bayesian probabilities and GB numbers are given
Fig. 1 in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 1. Proved occurrence of R. auricularia snails in Hungarian habitats based on museum collections and own investigations. The species was detected in artificial ponds or canals (yellow dots: living specimens; green dots: shells) and also in natural habitats (red dots: living specimens; blue dots: shells). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 8. a, b in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 8. a, b. Maximum likelihood tree of the samples of Trichobilharzia franki and Bilharziella polonica from the present study (a COI, b 28S) in relation to other schistostomatid sequences deposited in GenBank. Bootstrap values are given at the nodes; posterior probabilities for Bayesian inference are shown behind the bootstrap values. Unsupported nodes by BI are marked with a hyphen. Samples from the present study are in bold. The scale bar indicates the expected number of substitutions per sit.
Fig. 6. A in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 6. A hemalaun-stained Dendritobilharzia male from the liver of a mallard. Every scale under the specimen is equal to a millimetre.
Fig. 3. A in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 3. A complete specimen of native Trichobilharzia male in cell suspension from the liver of a mallard.
Fig. 2 in Threat of cercarial dermatitis in Hungary: A first report of Trichobilharzia franki from the mallard (Anas platyrhynchos) and European ear snail (Radix auricularia) using molecular methods
Fig. 2. The shape of bursa copulatrix of the adult R. auricularia is spherical and the stalk is long (A), while the bursa copulatrix of Radix balthica is oval and stalk is short (B). This anatomical structure seems the most reliable morphological difference to distinguish of the two most common Radix species in Hungary, but can only be studied on sexually mature and non-trematode infected specimens (Juh´asz, 2018) The length of the dissected organs is about 1 cm.
Figure 4 in A new Radix species from Qinling Mountains, China (Gastropoda: Lymnaeidae)
Figure 4. Median-joining network of the COI sequences of the Radix alticola species group (R. alticola, R. dgebuadzei sp. nov., R. euphratica, R. plicatula, and R. sp. Trichonis) (n=56). The red numbers near branches indicate the numbers of nucleotide substitutions between haplotypes. Size of circles corresponds to the number of available sequences for each haplotype (smallest circle = 1 sequence).
Figure 3 in A new Radix species from Qinling Mountains, China (Gastropoda: Lymnaeidae)
Figure 3. Maximum likelihood phylogeny of Radix species based on the COI barcode sequence dataset (n=56). Radix dgebuadzei sp. nov. is in red. Black numbers near nodes are bootstrap support values. Scale bar indicates the branch length.
Figure 2 in A new Radix species from Qinling Mountains, China (Gastropoda: Lymnaeidae)
Figure 2. Shell shape, mantle and foot pigmentations, and fragments of the reproductive system of lymnaeids: A) Radix dgebuadzei sp. nov., the holotype, shell (ZIN); B) R. dgebuadzei, shells of the paratypes (RMBH); C) R. dgebuadzei, mantle pigmentation, a paratype (RMBH); D) R. dgebuadzei, pigmentation on the back of the head, a paratype (RMBH); E) R. dgebuadzei, the copulatory apparatus of a paratype (RMBH); F) R. dgebuadzei, a fragment of the female reproductive system of the paratype (RMBH); G) R. plicatula, shells of samples from Sun Jia He River, China (RMBH); H) R. plicatula, mantle pigmentation (RMBH); I) R. plicatula, pigmentation on the back of the head (RMBH); J) R. euphratica, shells of samples from Tajikistan (RMBH); K) R. euphratica, mantle pigmentation (RMBH). Scale bar = 2 mm. (Photos: O.V. Aksenova, M.V. Vinarski).
Figure 1 in A new Radix species from Qinling Mountains, China (Gastropoda: Lymnaeidae)
Figure 1. Type locality of Radix dgebuadzei sp. nov.: A) general map revealing the position of the Qinling Mountains in China (red frame); B) geographic position of the type locality (red star); C) and D) the type locality: Sun Jia He River in the vicinity of the Shangtan village, Gansu Province, China (Maps: M.Yu. Gofarov; photos: V.S. Artamonova).
Fig 7 in An activity-integrated strategy of the identification, screening and determination of potential neuraminidase inhibitors from Radix Scutellariae
Fig 7. HCA dendrogram of 18 RS samples based on the NA inhibitory activity of compounds. Biennially cultivated RS (Group 1), perennially cultivated RS (Group 2), wild RS (Group 3) and plateau area RS (Group 4). https://doi.org/10.1371/journal.pone.0175751.g007
Fig 6 in An activity-integrated strategy of the identification, screening and determination of potential neuraminidase inhibitors from Radix Scutellariae
Fig 6. The relative NA inhibitory activity of baicalin, wogonin and wogonoside on HEK293Tcells. https://doi.org/10.1371/journal.pone.0175751.g006
Fig 3 in An activity-integrated strategy of the identification, screening and determination of potential neuraminidase inhibitors from Radix Scutellariae
Fig 3. Chromatogram of activity-integrated fingerprints of RS extracts. Chromatography (A) and total ion chromatography (B) of 26 compounds with NA inhibitory activity. Colored bar means the fraction collection purity> 98%. https://doi.org/10.1371/journal.pone.0175751.g003
Fig 2 in An activity-integrated strategy of the identification, screening and determination of potential neuraminidase inhibitors from Radix Scutellariae
Fig 2. Typical chromatogram. (A) RS extracts, (B) 9 standards mixture. Scutellarin (5), scutellarein (10), baicalin (11), chrysin-7-Oglucuronide (15), baicalein (19), wogonoside (22), wogonin (23), chrysin (24) and oroxylin A (25). https://doi.org/10.1371/journal.pone.0175751.g002
Fig 1 in An activity-integrated strategy of the identification, screening and determination of potential neuraminidase inhibitors from Radix Scutellariae
Fig 1. The principle of an activity integrated strategy method. The UPLC system with auto-fraction was used to separate, quantify collect and enrich the active compounds in fraction were performed by an. The fractions were used to test the bioactive analysis. https://doi.org/10.1371/journal.pone.0175751.g001
Fig 5 in An activity-integrated strategy of the identification, screening and determination of potential neuraminidase inhibitors from Radix Scutellariae
Fig 5. The cellular toxicity of baicalin, baicalein, wogonoside and wogonin. PLF and HIEC-6 cells were treated with indicated drugs with different concentrations as indicated for 24 hours and collected to evaluate cellular viability. https://doi.org/10.1371/journal.pone.0175751.g005
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