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427 results for “Ectoparasite”

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zenodo36/100

Figure 4 in Ectoparasite insects of bats from the fields and weedlands eco-region of Argentina

Figure 4. Hesperoctenes cartus (CMLA 766 ♀): (A) Ventral view, (B) Antenna and anterior leg, (C) Gular region and Prosternum.

opencc-by-nc-4.0Dec 2020View details →
zenodo36/100

Figure 2 in Ectoparasite insects of bats from the fields and weedlands eco-region of Argentina

Figure 2. Map of localities mentioned in text. The shaded area indicates the distribution of the Field and Weedlands Eco-region in the argentine provinces of Misiones and Corrientes. Localities were ordered alphabetically and correlatively numbered. Following the number, we offer the name of the specific locality, geographic coordinates and Province and Provincial Department, both in parenthesis. (1) Camping Japonés, Arroyo Yabebiry, Loreto (27°17′S, 55°30′W) (Misiones, Candelaria); (2) Candelaria (Misiones, Candelaria) (27°28′S, 55°45′W); (3) Candelaria, Balneario Arroyo Garupá (Misiones, Candelaria) (27°29′S, 55°44′W); (4) Estancia Prates, Barra Concepción (28°05′S, 55°32′W) (Misiones, Concepción); (5) Osununú (27°16′S, 55°34′W) (Misiones, San Ignacio); (6) Parque Provincial Cañadón de Profundidad (27°33′S, 55°42′W) (Misiones, Candelaria); (7) Parque Provincial de la Sierra "Ingeniero Agrónomo Martínez-Crovetto", Municipio de San José, 210 m (27°44′S, 55°33′W) (Misiones, Apóstoles); (8) Parque Provincial Teyú Cuaré (27°17′S, 55°35′W) (Misiones, San Ignacio); (9) Reserva Ecológica Tupá Puojhá (Fachinal) (27°37′S, 55°43′W) (Misiones, Capital); (10) Ruinas Santa María (27°53′S, 55°20′W) (Misiones, Concepción de la Sierra); (1) Yapeyú (29°28′S, 56°49′W) (Corrientes, General San Martín).

opencc-by-nc-4.0Dec 2020View details →
zenodo36/100

Figure 2 in Ectoparasitic flies (Diptera: Streblidae) on bats (Mammalia: Chiroptera) from a Private Natural Heritage Reserve in southeastern Brazil

Figure 2. Cluster analysis comparing studies carried out in five other Brazilian states: (1) Graciolli & Bianconi (2007) in Paraná, (2) Santos et al. (2009) in Maranhão, (3) Bertola et al. (2005) in São Paulo, (4) Komeno & Linhares (1999) in Minas Gerais, (5) Graciolli & Coelho (2001) in Distrito Federal, (6) the present study in Rio de Janeiro and (7) França et al. (2013) in Rio de Janeiro II.

opencc-by-nc-4.0Jan 2021View details →
zenodo36/100

Figure 1 in Ectoparasitic flies (Diptera: Streblidae) on bats (Mammalia: Chiroptera) from a Private Natural Heritage Reserve in southeastern Brazil

Figure 1. Location of the Bom Retiro Farm Private Natural Heritage Reserve (22°27′S, 42°18′W), Silva Jardim, Rio de Janeiro, southeastern Brazil.

opencc-by-nc-4.0Jan 2021View details →
dryad36/100

Impacts of male-killing Spiroplasma on the metabolic rate and ectoparasite resistance capacity (endurance) of Drosophila

<p>Ectoparasitic mites are hypothesized to horizontally transmit bacterial endosymbionts, especially male-killing Spiroplasma. In this study we test how <em>Spiroplasma poulsonii </em>MSRO affects fly physiology and behaviour, and potential mite interactions.</p>

opencc-zeroDec 2021View details →
dryad36/100

Phototaxic Behaviour of Flies with and without an ectoparasitic mite

<p>First, we demonstrated that flies are less likely to be infected by mites when exposed in light environments than dark environments using micro-arena experiments. In baseline conditions (mite-free environments), unmated female flies and mated female flies spent significantly more time in the dark side of the phototaxis chambers. Males did not show significant negative or positive phototaxis. Contrarily, when exposed to mites, neither unmated or mated females displayed significant phototaxis. Flies became less negatively phototaxic when threatened with mites, suggesting phototaxis is a mechanism of behavioural immunity.</p>

opencc-zeroDec 2021View details →
dryad36/100

Microclimate and host body condition influence mite population growth in a wild bird-ectoparasite system

<p>Parasite populations are never evenly distributed among the hosts they infect. Avian nest ectoparasites, such as mites, are no exception, as their distribution across the landscape is highly aggregated. It remains unclear if this pattern is driven by differences in transmission events alone, or if the environment that parasites inhabit after transmission also plays a role. Here, we experimentally examined the influence of the post-transmission microclimate, nest characteristics, and host condition on ectoparasite population growth in a bird-ectoparasite system. We infested barn swallow (Hirundo rustica erythrogaster) nests with a standardized number of Northern Fowl Mites (Ornithonyssus sylvarium) and analyzed both biotic (nestling mass, wing length, number of other arthropods present in the nest, and brood size) and abiotic (temperature, humidity, nest lining, nest dimensions, and substrate upon which the nest was built) predictors of mite population growth. Our results suggest that mite populations were most successful, in terms of growth, in nests with higher temperatures, lower humidity, few other arthropods, and hosts in good condition. We also found that nests built on wooden substrates support larger populations of mites than those constructed on metal or concrete. These findings lend insight into the factors that drive large-scale patterns of ectoparasite distributions.</p>

opencc-zeroMay 2022View details →
zenodo36/100

Figure 3 in Podapolipoides chorthippus n. sp. (Acari: Prostigmata: Podapolipidae), an ectoparasite of Chorthippus sp. (Orthoptera: Acrididae) from southern Iran

Figure 3 Podapolipoides chorthippusn. sp., male. A. Dorsal view. B. Ventral view.

opencc-by-4.0Jan 2022View details →
zenodo36/100

Figure 1 A in Podapolipoides chorthippus n. sp. (Acari: Prostigmata: Podapolipidae), an ectoparasite of Chorthippus sp. (Orthoptera: Acrididae) from southern Iran

Figure 1 A colony of Podapolipoides chorthippusn. sp. on pronotum of Chorthippus sp.

opencc-by-4.0Jan 2022View details →
zenodo36/100

Fig. 2 in Molecular detection of Wolbachia endosymbiont in reptiles and their ectoparasites

Fig. 2 Boa constrictor constrictor infested with Ophionyssus natricis (red arrows)

opencc-by-4.0Jul 2021View details →
zenodo36/100

Fig. 1 in Molecular detection of Wolbachia endosymbiont in reptiles and their ectoparasites

Fig. 1 Lacerta bilineata infested with Ixodes ricinus

opencc-by-4.0Jul 2021View details →
zenodo36/100

Fig. 3 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)

Fig. 3. Size structure of the population of Mauremys leprosa.

opencc-by-4.0Jun 2024View details →
zenodo36/100

Fig. 2 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)

Fig. 2. Morphometrical variables of Mauremys leprosa (for abbreviations see table 3).

opencc-by-4.0Jun 2024View details →
zenodo36/100

Fig. 2 in Ectoparasites of the critically endangered insular cavy, Cavia intermedia (Rodentia: Caviidae), southern Brazil

Fig. 2. Gliricola lindoiphoi male collected on Cavia intermedia. The bar corresponds to 100 μm.

opencc-by-4.0Apr 2015View details →
zenodo36/100

Fig. 1 in Ectoparasites of the critically endangered insular cavy, Cavia intermedia (Rodentia: Caviidae), southern Brazil

Fig. 1. Location map of Moleques do Sul Archipelago.

opencc-by-4.0Apr 2015View details →
zenodo36/100

Fig. 3 in Ectoparasites of the critically endangered insular cavy, Cavia intermedia (Rodentia: Caviidae), southern Brazil

Fig. 3. Trimenopon hispidum male collected on Cavia intermedia. The bar corresponds to 100 μm.

opencc-by-4.0Apr 2015View details →
zenodo36/100

Fig. 1 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 1. Prevalence of Lepeophtheirus sp in two size groups of Sciades herzbergii.

opencc-by-4.0Dec 2017View details →
zenodo36/100

Fig. 2 in Ectoparasites are unlikely to be a primary cause of population declines of bent-winged bats in south-eastern Australia

Fig. 2. Dorsal view of Penicillidia oceanica. Note absence of notopleural setae (Arrow).

opencc-by-4.0Dec 2018View details →
zenodo36/100

Fig. 1 in Ectoparasites are unlikely to be a primary cause of population declines of bent-winged bats in south-eastern Australia

Fig. 1. Dorsal view of Penicillidia tectisentis. Note notopleural setae (Arrow).

opencc-by-4.0Dec 2018View details →
zenodo36/100

The Effect of Forest Modification on Ectoparasite Density and Diversity

<b>Description: </b><p>Leech survey data</p><p><b>Project: </b>This dataset was collected as part of the following SAFE research project: <a href="https://www.safeproject.net/projects/project_view/24"><b>The Effect of Forest Modification on Ectoparasite Density and Diversity</b></a></p><p><b>XML metadata: </b>GEMINI compliant metadata for this dataset is available <a href="https://www.safeproject.net/datasets/xml_metadata?id=69">here</a></p><p><b>Data worksheets: </b>There are 2 data worksheets in this dataset:</p><ol><li><p><b>Morphometrics</b> (Worksheet BodyLength)</p><p>Dimensions: 809 rows by 5 columns</p><p>Description: Measurements of body length</p><p>Fields: </p><ul><li><b>Locality</b>: SAFE Project sample site (Field type: Location)</li><li><b>Species</b>: Species ID (Field type: Taxa)</li><li><b>Body Length</b>: Body length (Field type: Numeric Trait)</li><li><b>Date1</b>: Date leech was collected (Field type: Date)</li></ul><br></li><li><p><b>Survey data</b> (Worksheet SurveyData)</p><p>Dimensions: 188 rows by 12 columns</p><p>Description: Leech abundances and site observations</p><p>Fields: </p><ul><li><b>Plot</b>: SAFE Project sample site (Field type: Location)</li><li><b>Type</b>: Habitat type (Field type: Categorical)</li><li><b>Densiometer</b>: Canopy cover (Field type: Numeric)</li><li><b>Ground.Cover</b>: Density of understorey vegetation (Field type: Numeric)</li><li><b>Tiger.Leech.Number.(Haemadipsa.picta)</b>: Number of individuals collected (Field type: Abundance)</li><li><b>Brown.Leech.Number.(Haemadipsa.zeylanica)</b>: Number of individuals collected (Field type: Abundance)</li><li><b>Temperature</b>: Air temperature (Field type: Numeric)</li><li><b>Humidity.(RH%)</b>: Relative humidity (Field type: Numeric)</li><li><b>Soil.Surface.Moisture</b>: Soil surface moisture (Field type: Ordered Categorical)</li><li><b>Time</b>: Time survey was conducted (Field type: Time)</li><li><b>Reserve.Width.(m)</b>: Width of riparian strip (riparian sites only) (Field type: Numeric)</li></ul><br></li></ol><p><b>Date range: </b>2012-05-05 to 2012-06-21</p><p><b>Latitudinal extent: </b>4.6353 to 4.7533</p><p><b>Longitudinal extent: </b>116.9477 to 117.6581</p><p><b>Taxonomic coverage: </b><br> All taxon names are validated against the GBIF backbone taxonomy. If a dataset uses a synonym, the accepted usage is shown followed by the dataset usage in brackets. Taxa that cannot be validated, including new species and other unknown taxa, morphospecies, functional groups and taxonomic levels not used in the GBIF backbone are shown in square brackets.</p><div>Animalia<br>&ensp;-&ensp;Annelida<br>&ensp;-&ensp;&ensp;-&ensp;Clitellata<br>&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;Arhynchobdellida<br>&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;Haemadipsidae<br>&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;<i>Haemadipsa</i><br>&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;<i>Haemadipsa zeylanica</i><br>&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;<i>Haemadipsa</i><br>&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;&ensp;-&ensp;<i>Haemadipsa picta</i><br></div><p></p>

opencc-by-4.0Mar 2018View details →

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Last verified 2026-04-29Open record