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Fig. 4 in Outcome of within-host competition demonstrates that parasite virulence doesn't equal success in a myxozoan model system

Fig. 4. Total number of a) genotype-I and b) genotype-II myxospores produced per actinospore, as a measure of parasite success, in fish from single and mixedgenotype treatments. Black bars denote genotype-I only, white denote genotype-II only, and grey denote mixed-genotype treatments. Letters indicate treatments that differed (Tukey's HSD tests, α = 0.05).

opencc-by-4.0Aug 2019View details →
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Fig. 3 in Outcome of within-host competition demonstrates that parasite virulence doesn't equal success in a myxozoan model system

Fig. 3. Parasite copy number, as a measure of parasite competition in mixed-genotype treatments, in a) gill tissue sampled at 7d (t7), b) gill tissue sampled at 14d (t14) c) intestinal tissue sampled at 7d, and d) intestinal tissue sampled at 14d. Black bars denote genotype-I only, white denote genotype-II only, and grey denote mixedgenotype treatments. Inset striped grey bars represent total genotype I copy numbers, based on the proportion of genotype I in sequenced DNA samples (genotype II comprises the remainderthe solid grey bar). Letters indicate treatments that differed (Tukey's HSD tests, α = 0.05). Total number of genotype-I (black circles) and genotype-II (white circles) myxospores produced per actinospore, as a measure of parasite success in fish overlaid on parasite copy number in intestinal tissue sampled at 14d.

opencc-by-4.0Aug 2019View details →
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Fig. 4 in A community analysis approach to parasite transmission in multi-host systems: Assemblages of small mammal prey and Echinococcus multilocularis in an urban area in North America

Fig. 4. Map showing the geographic distribution of three small mammal assemblage types predicted for the City of Calgary area by a multinomial logistic regression (MLR) model associating the environmental variables to assemblage types, developed from data collected in 2012 and 2013 (Liccioli et al., 2014). Note how large portion of BWM and NHP were classified as assemblage 1 as expected, but also large portion of FCPP, where it was not expected.

opencc-by-4.0Aug 2019View details →
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Fig. 1 in A community analysis approach to parasite transmission in multi-host systems: Assemblages of small mammal prey and Echinococcus multilocularis in an urban area in North America

Fig. 1. Study sites for the characterization of the small mammal assemblages in urban Calgary, AB, Canada in 2012–2013, showing the location of five areas in Urban Calgary and detailed map of Bowmont, Southland Lowlands, and Weaselhead. Bowmont (BM), Fishcreek Provincial Park (FCPP), Nose Hill Park (NHP), Southland Lowlands (SL), and Weaselhead (WSH).

opencc-by-4.0Aug 2019View details →
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Fig. 2 in Outcome of within-host competition demonstrates that parasite virulence doesn't equal success in a myxozoan model system

Fig. 2. Median day to death, as a measure of parasite virulence, in treatment groups. Black bars denote genotype-I only, white denote genotype-II only, and grey denote mixed-genotype treatments. Letters indicate treatments that differed (Tukey's HSD tests, α = 0.05).

opencc-by-4.0Aug 2019View details →
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Fig. 1 in Outcome of within-host competition demonstrates that parasite virulence doesn't equal success in a myxozoan model system

Fig. 1. Experimental schematic and timeline. Timeline begins at t-3 when density of parasites in polychaete cultures (inset a) was estimated in replicate water samples to calculate dose administered on t0 and t6. Specific-pathogen-free (SPF) well water ("W") was used as a negative control and a mock exposure t0 and t6 in treatments that received no parasites on those exposure dates "W"- denotes water, "I: denotes genotype-I and "II" denotes genotype-II (inset b). * denote treatments used for cytokine and immunoglobulin assays (b).

opencc-by-4.0Aug 2019View details →
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Fig. 1 in Role of temperature and carbonate system variability on a host-parasite system: Implications for the gigantism hypothesis

Fig. 1. Study sites along the Chilean coast (Quintay and Concepción), and variability in temperature, pH, salinity, total alkalinity, partial pressure of CO2, and aragonite saturation state. Bars indicate ± 1 standard error. Asterisk represents significant differences between sites (p <0.001).

opencc-by-4.0Aug 2019View details →
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Fig. 2 in A community analysis approach to parasite transmission in multi-host systems: Assemblages of small mammal prey and Echinococcus multilocularis in an urban area in North America

Fig. 2. Dendrograms derived from the Bray-Curtis similarity of small mammal assemblages in five parks and natural areas in urban Calgary, AB, Canada, 2012–2013. a) Dendrogram using abundance data and group-average clustering algorithm. The dashed line indicates the cluster cut-off line of 45% similarity. Symbols for each site indicate the prevalence of definitive hosts (EmDH) and presence (1) or absence (0) of infected small mammals (EmIH). b) Dendrogram using abundance data and complete-linkage clustering algorithm. Note how it is similar to the dendrogram using group-average algorithm. c) Dendrogram using proportion data and group-average clustering algorithm. Note how all BM sites are in single cluster and all NHP sites and most sites are in another cluster, similar to the dendrogram using abundance data.

opencc-by-4.0Aug 2019View details →
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Fig. 2. A in Multiple infestations of gastrointestinal parasites - Probable cause for high mortality of Spot-billed Pelican (Pelecanus philippensis) at Kokrebellur Community Reserve, India

Fig. 2. A. Larvae of Contracaecum sp. in fish, B. Adult Contracaecum sp. worms in the pelican, C. Eggs of Echinostoma sp. in pelican fecal and water samples, D. Eggs of Contracaecum sp. in pelican fecal and water samples and E. Eggs of Opisthorchis viverrini in pelican fecal samples.

opencc-by-4.0Aug 2019View details →
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Figure 8 in Taxonomical studies of four new Aseptate Gregarine parasites belonging to the Genus Monocystis Stein, 1848 (Protozoa: Apicomplexa: Sporozoa) from an Oligochaete Host, Eutyphoeus orientalis (Annelida: Oligochaeta) of West Bengal, India

Figure 8. Monocystis csabai sp. nov. (Camera lucida drawings of different stages of life cycle) A. Trophozoite. B. Syzygy. C. Gametocyst D. Oocyst. Scales: A-C = 100µm; D = 10µm.

opencc-by-4.0Dec 2019View details →
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Figure 6 in Taxonomical studies of four new Aseptate Gregarine parasites belonging to the Genus Monocystis Stein, 1848 (Protozoa: Apicomplexa: Sporozoa) from an Oligochaete Host, Eutyphoeus orientalis (Annelida: Oligochaeta) of West Bengal, India

Figure 6. Monocystis satoi sp. nov. (Camera lucida drawings of different stages of life cycle) A-B. Trophozoite. C. Syzygy D. Gametocyst. E. Oocyst. Scales: A-D =100µm; E=10µm.

opencc-by-4.0Dec 2019View details →
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Figure 3 in Taxonomical studies of four new Aseptate Gregarine parasites belonging to the Genus Monocystis Stein, 1848 (Protozoa: Apicomplexa: Sporozoa) from an Oligochaete Host, Eutyphoeus orientalis (Annelida: Oligochaeta) of West Bengal, India

Figure 3. Monocystis indicus sp. nov. (Photomicrographs of different stages of life cycle) A. Trophozoite (white arrow – granulated endosarc). B. Syzygy. C. Gametocyst. D. Oocyst. Scales: A-C = 100µm, D = 10µm.

opencc-by-4.0Dec 2019View details →
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Figure 4 in Taxonomical studies of four new Aseptate Gregarine parasites belonging to the Genus Monocystis Stein, 1848 (Protozoa: Apicomplexa: Sporozoa) from an Oligochaete Host, Eutyphoeus orientalis (Annelida: Oligochaeta) of West Bengal, India

Figure 4. Monocystis indicus sp. nov. (Camera lucida drawings of different stages of life cycle) A. Trophozoite. B. Syzygy. C. Gametocyst. D. Oocyst. Scales: A-C =100µm; D = 10µm.

opencc-by-4.0Dec 2019View details →
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Figure 7 in Taxonomical studies of four new Aseptate Gregarine parasites belonging to the Genus Monocystis Stein, 1848 (Protozoa: Apicomplexa: Sporozoa) from an Oligochaete Host, Eutyphoeus orientalis (Annelida: Oligochaeta) of West Bengal, India

Figure 7. Monocystis csabai sp. nov. (Photomicrographs of different stages of life cycle) A. Trophozoite (white arrow- large rounded distinct nucleus); (black arrow- tapering pointed end). B. Syzygy. C. Gametocyst D. Oocyst. Scales: A-C = 100µm; D = 10µm.

opencc-by-4.0Dec 2019View details →
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Figure 1 in Taxonomical studies of four new Aseptate Gregarine parasites belonging to the Genus Monocystis Stein, 1848 (Protozoa: Apicomplexa: Sporozoa) from an Oligochaete Host, Eutyphoeus orientalis (Annelida: Oligochaeta) of West Bengal, India

Figure 1. Photomicrographs of different stages of the life history of Monocystis eutyphae sp. nov. obtained from the seminal vesicles of earthworm Eutyphoeus orientalis, A. Trophozoite(Black arrow - mucron); (white arrow - granulated endosarc). B. Syzygy. C. Gametocyst. D. Oocyst. Scales: A - C = 100µm; D = 10µm

opencc-by-4.0Dec 2019View details →
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Figure 1 in Detection of helminth parasites in commercialized turtles: threats to native Testudines in northeast India

Figure 1. Astiotrema reniferum: (A) entire, ventral view (arrow marks anterior to posterior denoted ovary, anterior testis, and posterior testes), (B) Anterior end, ventral view (arrow marks anterior to posterior denoted oral sucker, gonopore, acetabulum, and ovary), (C) Gonopore, and egg are marked by arrow anterior to posterior, and (D) Testes, ventral view.

opencc-by-4.0Dec 2020View details →
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Figure 2. A in First record of parasitism in Avicularia purpurea Kirk, 1990 (Araneae: Theraphosidae: Aviculariinae) by Notocyphus aff. tyrannicus Smith, 1855 (Hymenoptera: Notocyphinae) in the Ecuadorian Amazon

Figure 2. A. Localities of A. purpurea in Ecuador. B. Juvenile individual of A. purpurea that presented the parasitic larvae of Notocyphus aff. tyrannicus. C. Live adult of N. aff. tyrannicus. Scale bar: 1 cm.

opencc-by-4.0Mar 2021View details →
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Figure 3. A in First record of parasitism in Avicularia purpurea Kirk, 1990 (Araneae: Theraphosidae: Aviculariinae) by Notocyphus aff. tyrannicus Smith, 1855 (Hymenoptera: Notocyphinae) in the Ecuadorian Amazon

Figure 3. A. Dorsal view of N. aff. tyrannicus. B. Front view. C. Side view. D. Cocoon of N. aff. tyrannicus. E. Silk shelter made by A. purpurea, note the cocoon at one end. F. Wing detail of N. aff. tyrannicus. Scale bar: 1 cm.

opencc-by-4.0Mar 2021View details →
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Figure 1 in First record of parasitism in Avicularia purpurea Kirk, 1990 (Araneae: Theraphosidae: Aviculariinae) by Notocyphus aff. tyrannicus Smith, 1855 (Hymenoptera: Notocyphinae) in the Ecuadorian Amazon

Figure 1. Locality where the specimen of A. purpurea parasitized by Notocyphus af. tyrannicus was collected. / Localidad de recolección del especímen de A. purpurea parasitado por Notocyphus af. tyrannicus.

opencc-by-4.0Mar 2021View details →
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Figure 1. A in New molecular data for parasites Hammerschmidtiella indicus and Thelandros scleratus (Nematoda: Oxyurida) to infer phylogenetic position

Figure 1. A phylogenetic tree based on the 18S rDNA sequences was constructed by using the ME method. The evolutionary distance values are indicated at the nodes. The GenBank accession number for each sequence is given adjacent to the name of the corresponding species.

opencc-by-4.0Feb 2015View details →

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Last verified 2026-04-29Open record