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116 results for “Host Parasite Interactions”

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zenodo40/100

Fig. 2 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 2. Schematic representation of the experimental system used to test the host selection behavior of the isopods in the single-host treatments. A: Tachaea chinensis at 20-min acclimation. B: T. chinensis after release.

opencc-by-4.0Aug 2023View details →
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Fig. 3 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 3. Schematic representation of the experimental system used to test the host selection behavior of the isopods in the common vs un-common host treatments. A: Tachaea chinensis at 20-min acclimation. B: T. chinensis after release.

opencc-by-4.0Aug 2023View details →
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Fig. 7 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 7. Average predation proportion of Tachaea chinensis in each freshwater decapod's species treatment. Fishers exact test, *P <0.05, **P <0.01.

opencc-by-4.0Aug 2023View details →
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Fig. 9 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 9. Attachments of Tachaea chinensis on various freshwater decapods during this study. The arrows indicate the position of the isopod on the host. (a) T. chinensis on the left-side of the carapace of Palaemon paucidens; (b) T. chinensis on the right-side of the carapace of Procambarus clarkii; (c) T. chinensis attached on the right-side of the carapace of Neocaridina spp.; and (d) T. chinensis initially clinging on the abdomen of Macrobrachium nipponense.

opencc-by-4.0Aug 2023View details →
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Fig. 5 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 5. Selection percentage of Tachaea chinensis in the single-host treatments. Each treatment was repeated 10 times (one isopod per treatment); *: P <0.05, ***: P <0.001, ****: P <0.0001 (Binomial test of significance).

opencc-by-4.0Aug 2023View details →
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Fig. 1 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 1. Eight different host options were used to investigate the host selection of Tachaea. chinensis isopods. (a) Palaemon paucidens; (b) Palaemon sinensis; (c) Neocaridina spp.; (d) Macrobrachium nipponense; (e) Procambarus clarkii; (f) Rhodeus ocellatus; (g) Oryzias latipes and (h) Artificial P. paucidens.

opencc-by-4.0Aug 2023View details →
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Fig. 4 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 4. The experimental system used to test the potential predation of Tachaea chinensis by freshwater host species.

opencc-by-4.0Aug 2023View details →
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Fig. 10 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 10. Prey handling procedure of the crayfish Procambarus clarkii (carapace length: 19 mm). (1) the crayfish P. clarkii approaching an 8 mm body length Tachaea chinensis; (2)–(5) P. clarkii catching and manipulating the prey using its pair of chelipeds; (6)–(8) the crayfish began consuming the prey by placing it directly into its mandibles.

opencc-by-4.0Aug 2023View details →
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Fig. 6 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 6. Selection percentage of Tachaea chinensis when subjected to un-common host selection experiments. Each treatment was repeated 10 times (one isopod per treatment); ***: P <0.001 (Binomial test of significance).

opencc-by-4.0Aug 2023View details →
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Fig. 8 in Host selection and potential predation in the host-parasite interaction between the isopod Tachaea chinensis and freshwater host species

Fig. 8. Number of Tachaea chinensis predated by; Palaemon paucidens, Macrobrachium nipponense and Procambarus clarkii. A total of 20 T. chinensis isopods (two isopods per trials, 10 replications) were used in each treatment.

opencc-by-4.0Aug 2023View details →
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Fig. 3 in Host-parasite interactions between the piranha Pygocentrus nattereri (Characiformes: Characidae) and isopods and branchiurans (Crustacea) in the rio Araguaia basin, Brazil

Fig. 3. Correlation between the standard length of Pygocentrus nattereri and the number of branchiurans (intensity of infestation) in lakes and an oxbow lake at the rio Araguaia, State of Goiás, Amazon basin. (rs= 0.2397, p= 0.0001).

opencc-by-4.0Jun 2004View details →
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Fig. 2. The circle outlines a in Host-parasite interactions between the piranha Pygocentrus nattereri (Characiformes: Characidae) and isopods and branchiurans (Crustacea) in the rio Araguaia basin, Brazil

Fig. 2. The circle outlines a tumor (a) observed on Pygocentrus nattereri, possibly caused by the action of the isopod Braga patagonica (b).

opencc-by-4.0Jun 2004View details →
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Fig. 1 in Host-parasite interactions between the piranha Pygocentrus nattereri (Characiformes: Characidae) and isopods and branchiurans (Crustacea) in the rio Araguaia basin, Brazil

Fig. 1. Relative frequencies (%) of attachment sites of branchiurans on Pygocentrus nattereri (Serrasalminae) in the Amazon basin.

opencc-by-4.0Jun 2004View details →
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Can predators stabilize host-parasite interactions? Changes in aquatic predator identity alters amphibian responses and parasite abundance across life stages

<p><span><span>The role of parasites can change depending on the food web community. Predators, for instance, can amplify or dilute parasite </span><span>effects on their hosts. Likewise, exposure to parasites or predators at one life stage can have long-term consequences on individual performance and survival, which can influence population and disease dynamics. To understand how predators affect amphibian parasite infections across life stages, we manipulated exposure of northern leopard frog (<em>Rana pipiens</em>) tadpoles to three predators (crayfish [<em>Orconectes rusticus</em>], bluegill [<em>Lepomis macrochirus</em>], or mosquitofish [<em>Gambusia affinis</em>]) and to trematode parasites (<em>Echinostoma</em> spp.) in mesocosms and followed juveniles in outdoor terrestrial enclosures through overwintering. Parasites and predators both had strong impacts on metamorphosis with bluegill and parasites individually reducing metamorph survival. However, when fish were present, the negative effects of parasites on survival were not apparent, likely because fish altered community composition via increased algal food resources. Bluegill also reduced snail abundance, which could explain the reduced abundance of parasites in surviving metamorphs. Bluegill and parasite exposure increased mass at metamorphosis, which increased metamorph jumping, swimming, and feeding performance, suggesting larger frogs would experience better terrestrial survival. Effects on size at metamorphosis persisted in the terrestrial environment but did not influence overwintering survival. Based on our results, we constructed stage-structured population models to evaluate the lethal and sublethal effects of bluegill and parasites on population dynamics. Our models suggested that the positive effects of bluegill and parasites on body size may have greater effects on population growth than the direct effects of mortality.</span> <span>This study illustrates how predators can alter the outcome of parasitic infections and highlights the need for long-term experiments that investigate how changes in host-parasite systems alter population dynamics. We show some predators reduce parasite effects and have indirect positive effects on surviving individuals potentially increasing host population persistence. </span></span></p>

opencc-zeroOct 2022View details →
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Figure 1 in Parasites as secret files of the trophic interactions of hosts: the case of the rufousbellied thrush Los parásitos como archivos secretos en las interacciones tróficas con sus hospederos: el caso del Zorzal Colorado

Figure 1. Relationship between body weight in grams (independent variable) of adult rufous-bellied thrushes (Turdus rufiventris) and species richness of parasites (dependent variable).

opencc-by-4.0Nov 2010View details →
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Data for: Temperature and intraspecific variation affect host-parasite interactions

<p>Parasites play key roles in regulating aquatic ecosystems, yet the impact of climate warming on their ecology and disease transmission remains poorly understood. Isolating the effect of warming is challenging as transmission involves multiple interacting species and potential intraspecific variation in temperature responses of one or more of these species. Here, we leverage a wide-ranging mosquito species and its facultative parasite as a model system to investigate the impact of temperature on host-parasite interactions and disease transmission. We conducted a common garden experiment measuring parasite growth and infection rates at seven temperatures using 12 field-collected parasite populations and a single mosquito population. We find that both free-living growth rates and infection rates varied with temperature, which were highest at 18-24.5°C and 13°C, respectively. Further, we find intraspecific variation in peak performance temperature reflecting patterns of local thermal adaptation—parasite populations from warmer source environments typically had higher thermal optima for free-living growth rates. For infection rates, we found a significant interaction between parasite population and nonlinear effects of temperature. These findings underscore the need to consider both host and parasite thermal responses, as well as intraspecific variation in thermal responses, when predicting the impacts of climate change on disease in aquatic ecosystems.</p>

opencc-zeroSep 2023View details →
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Ancient diversity in host-parasite interaction genes in a model parasitic nematode

<p>Files associated with the &quot;Ancient diversity in host-parasite interaction genes in a model parasitic nematode&quot; manuscript.&nbsp;</p> <p><strong>VCF files:</strong></p> <p>HB1_vs_nxHelBake1.biallelic_noRefCall.qual.repeat_filtered.vcf.gz<br> HB2_vs_nxHelBake1.biallelic_noRefCall.qual.repeat_filtered.vcf.gz<br> HB3_vs_nxHelBake1.biallelic_noRefCall.qual.repeat_filtered.vcf.gz<br> HP1_vs_ngHelPoly1.biallelic_noRefCall.qual.repeat_filtered.vcf.gz<br> HP2_vs_ngHelPoly1.biallelic_noRefCall.qual.repeat_filtered.vcf.gz</p> <p><strong><em>H. mixtum</em> genome assemblies:</strong><br> Hm16_merged_spades_scaffolds.fa.gz<br> Hm2_merged_spades_scaffolds.fa.gz</p> <p><strong>Strongylomorph phylogeny:</strong></p> <p>Strongylomorph_phylogeny_18Jan2023_20spp_511orthos.astral.nwk.gz</p> <p><strong>Gene annotation files:</strong><br> ngHelPoly1.1.primary.final_annotations.cds.fa.gz<br> ngHelPoly1.1.primary.final_annotations.gff3.gz<br> ngHelPoly1.1.primary.final_annotations.proteins.fa.gz</p> <p>nxHelBake1.1.primary.final_annotations.cds.fa.gz<br> nxHelBake1.1.primary.final_annotations.gff3.gz<br> nxHelBake1.1.primary.final_annotations.proteins.fa.gz</p> <p><strong>Curated repeat libraries:</strong><br> ngHelPoly1.1.repeats.01062023.fa.gz<br> nxHelBake1.1.repeats.01062023.fa.gz</p> <p><strong>Assembled transcripts:</strong></p> <p>ngHelPoly1_hq_transcripts.fa.gz</p> <p>nxHelBake1_hq_transcripts.fa.gz</p>

openmit-licenseOct 2023View details →
dryad40/100

Can predators stabilize host-parasite interactions? Changes in aquatic predator identity alters amphibian responses and parasite abundance across life stages

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publicNov 2022View details →
dryad40/100

Data for: Temperature and intraspecific variation affect host-parasite interactions

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publicSep 2023View details →
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Data from: The interactive effects of heat stress, parasitism, and hostplant quality in a host-parasitoid system

Open the record for dataset details and reuse information.

publicDec 2023View details →

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