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Fig. 3 in Detection of cryptic species of Rugopharynx (Nematoda: Strongylida) from the stomachs of Australian macropodid marsupials

Fig. 3. Phylogenetic relationships of species of Rugopharynx and Rugonema labiatum based on a Bayesian analysis of the sequence data of the ITS+ nuclear ribosomal DNA. Values above branches indicate posterior probabilities that were greater than 0.8. Abbreviations of Australian state names are provided in Table 1.

Fig. 2 in Detection of cryptic species of Rugopharynx (Nematoda: Strongylida) from the stomachs of Australian macropodid marsupials

Fig. 2. Morphological buccal capsule types in the genus Rugopharynx. I, simple cylindrical buccal capsule, R. macropodis; IIA, bilobed buccal capsule with subequal divisions, R. epsilon; IIB, bilobed buccal capsule with anterior lobe shorter, R. rufogrisea; III, trilobed buccal capsule, R. longibursaris.

Fig. 1 in Detection of cryptic species of Rugopharynx (Nematoda: Strongylida) from the stomachs of Australian macropodid marsupials

Fig. 1. Localities within Australia at which specimens of Rugopharynx used in this study were collected. Coordinates for each locality are provided in Table 1. 1, Lake Clifton; 2, Waroona; 3, Collie, Wellington Dam; 4, Perup River; 5, Kalgoorlie; 6, Wallerberdina Station; 7, Port Augusta; 8, Ashbourne; 9, Kangaroo Island; 10, Naracoorte; 11, Hattah Lakes National Park; 12, Yan Yean; 13, The Gurdies; 14, Launceston; 15, Emu Flat, Bondo State Forest; 16, Trangie; 17, Grafton; 18, Lamington National Park; 19, Miles; 20, Dawes; 21, Mt Sebastopol; 22, Rockhampton; 23, Winton; 24, Proserpine; 25, Bowen; 26, Magnetic Island; 27, Lake Barrine.

Fig. 5 in Detection of cryptic species of Rugopharynx (Nematoda: Strongylida) from the stomachs of Australian macropodid marsupials

Fig. 5. Molecular phylogeny of species of Rugopharynx and Rugonema labiatum based on a consensus of the BI, NJ and MP trees (Figs. 3 and 4), and the relationships of their hosts. This figure includes species of Macropus (M. agilis, M. antilopinus, M. bernardus) which are not hosts to species of Rugopharynx, as well as M. parma, from which no material could be obtained for genetic studies. Only those species of Petrogale included in this study are shown on the host tree. The morphology of the buccal capsule for each nematode taxon is also shown.

Fig. 3 in Evaluation of the stomach contents of Eriphia gonagra from a rocky shore in the southeastern Brazilian coast

Fig. 3. Percentage of itens found in the stomachs of Eriphia gonagra (Fabricius, 1781) captured in the rocky shores (RO) and sand reefs (SR) of Praia Grande, Ubatuba (São Paulo, Brazil). Other animals on RO (0.3%) and SR (0.2%), as well as the presence of nylon threads (RO = 0.05%; SR = 0.06%) are not visible in the figure.

Fig. 6 in Evaluation of the stomach contents of Eriphia gonagra from a rocky shore in the southeastern Brazilian coast

Fig. 6. Frequency of the composition of the main items of the Eriphia gonagra (Fabricius, 1781) diet, according to size classes.

Fig. 2 in Evaluation of the stomach contents of Eriphia gonagra from a rocky shore in the southeastern Brazilian coast

Fig. 2. Percentage of the main food items found in the stomachs of males, females and total population of Eriphia gonagra (Fabricius, 1781) captured on the rocky shore of Praia Grande beach, Ubatuba, São Paulo, Brazil.

Fig. 5 in Evaluation of the stomach contents of Eriphia gonagra from a rocky shore in the southeastern Brazilian coast

Fig. 5. Correspondence Analysis (CA) of frequency of the most relevant food item in the stomachs of males and females of Eriphia gonagra (Fabricius, 1781) at different sampling points of Praia Grande beach, Ubatuba, São Paulo, Brazil.

Fig. 1 in Evaluation of the stomach contents of Eriphia gonagra from a rocky shore in the southeastern Brazilian coast

Fig. 1. Map of Ubatuba Bay with the sampling area between Praia Grande and TenÓrio beaches, state of São Paulo, Brazil.

Fig. 4 in Evaluation of the stomach contents of Eriphia gonagra from a rocky shore in the southeastern Brazilian coast

Fig. 4. Percentage of itens found in the stomachs of Eriphia gonagra (Fabricius, 1781) captured over the seasons in the rocky shores (RO) and sand reefs (SR) of Praia Grande, Ubatuba (São Paulo, Brazil).

opencc-by-4.0Apr 2024View details →

Fig. 3 in Studies on the embryonic development and larval infection potential of the stomach bot flies, Gasterophilus pecorum

Fig. 3. Life history of G. pecorum and prediction of egg state larvae population. Note: The survival period of egg state larvae of G. pecorum at different temperatures (a); The monthly average temperatures in Kalamaili nature reserve (KNR) in recent ten years (b); Changes in parasite population in vitro of the host (c), +: mild; ++: moderate; +++: considerable; ++++: severe; ⸭: potential.

opencc-by-4.0Apr 2024View details →

Fig. 1 in Studies on the embryonic development and larval infection potential of the stomach bot flies, Gasterophilus pecorum

Fig. 1. The relationship between the embryonic development period and the temperature of G. pecorum.

opencc-by-4.0Dec 2010View details →

Figure 3 in Do male tree frogs feed during the breeding season? Stomach flushing of five syntopic hylid species in Rio Grande do Sul, Brazil

Figure 3. Relation between length of the reproductive period and food intake by 50 males per species.

opencc-by-4.0Dec 2008View details →

Fig. 6 in Scientific Note Stomach contents and notes on the reproduction of the Onefin Skate Gurgesiella dorsalifera (Chondrichthyes: Rajidae) off Southern Brazil

Fig. 6. Ventral view of visceral cavity of G. dorsalifera. OG = horseshoe shaped oviducal gland; EC = egg capsules inside the uteri; CL = extroverted cloaca.

opencc-by-4.0Dec 2008View details →

Fig. 1 in Scientific Note Stomach contents and notes on the reproduction of the Onefin Skate Gurgesiella dorsalifera (Chondrichthyes: Rajidae) off Southern Brazil

Fig. 1. Map of the study region with marks where specimens of Gurgesiella dorsalifera were captured: 1 – 1986 one specimen; 2 – 1991 eight specimens and 3 – 1991 fifteen specimens.

opencc-by-4.0Jun 2021View details →

The Influence of Lactobacillus Acidophilus on MUC1, GAL-3, IL-1β and IL-17 Gene Expression in BALB/c Mice Stomach

Gene expression of MUC-1, GAL-3, IL-1 and IL-17 after treatment with low, moderate and high doses of Lactobacillus acidophilus ATCC 4356   in mice

opencc-by-4.0Nov 2024View details →

cumt6527/Stomach-images-and-pig-stomach-images: Stomach-images-and-pig-stomach-images

No description provided.

opencc-by-4.0May 2022View details →

Raw sequencing data of NGS of stomach contents of sympatric species of weakly electric fish (genus: Campylomormyrus)

This dataset contains the raw sequencing data of stomach contents of sympatric species of weakly electric fish (genus: Campylomormyrus) using next generation sequencing. Stomach content samples were collected from five Campylomormyrus species (C. alces, ; C. compressirostris, ; C. curvirostris, ; C. numenius, ; C. tshokwe) and samples of Gnathonemus petersii (G. petersii, ), a sister genus of Campylomormyrus. The fish specimens, from which these stomach content samples are extracted, were collected during an expedition to the Republic of the Congo in fall 2012. The dataset files are in FASTA format.

opencc-by-4.0May 2024View details →

Stomach as the target organ of Rickettsia heilongjiangensis infected C57BL/6 mice identified by click chemistry

Code used for analyses and generate figures in the manuscript *Stomach as the target organ of Rickettsia heilongjiangensis infected C57BL/6 mice identified by click chemistry*. Input and scripts are included in corresponding files.