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10,635 results for “Mites”
Data from: Thermal niches of wheat curl mite, Aceria tosichella (Acari: Eriophyidae): congruence between physiological and geographical distribution data
<p><strong>Filename: parm.csv</strong></p> <p>Population growth rate of the two wheat curl mite (WCM) lineages reared in different temperatures.</p> <ol> <li>lineage - mitochondrial lineage (MT-1 or MT-8)</li> <li>temp - the rearing temperature (ºC)</li> <li>n - no. of replications of the experiment</li> <li>r, r.lower, r.upper - estimated intrinsic population growth rate and its 95% confidence intervals</li> </ol> <p><strong>Filename: aceria.csv</strong></p> <p>Data on field sampling localities, WCM abundance and thermal niche suitabiity.</p> <ol> <li>julian - Julian date</li> <li>x, y - geodetic coordinates (EPSG: 2180)</li> <li>stems - no. of stems collected</li> <li>MT1, MT8- mitochondrial lineage (MT-1 or MT-8)</li> <li>TNS1, TNS8 - thermal niche suitability for lineages</li> </ol>
Data from: Spatial and host-related variation in prevalence and population density of wheat curl mite (Aceria tosichella) cryptic genotypes in agricultural landscapes
<p><strong>Filename: coord.csv</strong></p> <p>Names of the sampling locations and their geographic coordinates.</p> <ol> <li>Name - sampling locality identifier</li> <li>Lat - latitude</li> <li>Long - longitude</li> </ol> <p> </p> <p><strong>Filename: lineages.csv</strong></p> <ol> <li>id.sample - sample identifier</li> <li>host - host species (Arrela=<em>Arrhenantherum elatius</em>, Avesat=<em>Avena sativa</em>, Broine=<em>Bromus inermis</em>, Elyres=<em>Elymus repens</em>, Horvul=<em>Hordeum vulgaris</em>, Seccer=<em>Secale cereale</em>, Triaes=<em>Triticum aestivum</em>, Tririm=<em>Triticale rimpaui</em></li> <li>x, y - geodetic coordinates</li> <li>stems - no. of stems in a sample</li> <li>leaves - no. of leaves in a sample</li> <li>MT.01 to MT.27 - no. of mites belonging to each genetic lineage</li> </ol>
Data from: Behavioural responses to potential dispersal cues in two economically important cereal-feeding eriophyoid mite species
<p>Variables:</p> <ol> <li>species (ABH = <em>Abacarus hystrix</em>, WCM = <em>Aceria tosichella</em> MT1 genetic lineage)</li> <li>variant - experimental treatment (type of dispersal cue): wind, an insect vector, presence of a fresh plant</li> <li>feeding - no. of feeding specimens</li> <li>walking - no. of walking specimens</li> <li>standing - no. of specimens standing vertically</li> <li>cha - no. of specimens forming chains</li> <li>mob - no. of specimens capable to move</li> <li>pop - no. of all specimens (including quiescent stages)</li> </ol>
Habitat fragmentation mite data, South Carolina, 2018
These csv files contain mite abundance and richness data, fungal abundance data, and leaf characteristics used in the paper "The impact of habitat fragmentation on domatia-dwelling mites and a mite-plant-fungus tritrophic interaction" published in Landscape Ecology in 2022. The project was conducted at the Savannah River Site, near Aiken, South Carolina, United States during the summer of 2018. The goal of the project was to assess the impacts of landscape-level habitat fragmentation on communities of mites and fungi on leaf surfaces growing on Quercus nigra oak trees within landscape patches. To investigate this, we counted and morphotyped mites found on leaves taken from oaks located in habitat patches manipulated to have different edge-to-area ratios and connectivity statuses. We also manipulated mite access to domatia on oak leaves using a tar treatment, and assessed whether mite exclusion and landscape fragmentation variables influenced levels of fungal hyphae on oak leaves. We found a significant positive effect of patch edge proximity on mite abundance and richness, as well as fungal hyphae abundance, indicating that landscape-level habitat fragmentation can impact microscopic foliar communities.
Effects of microarthropod exclusion and water amendments on fluffgrass growth, root nitrogen, and mite and nematode abundance at the Jornada Basin LTER site, 1986-1987
This data package contains data on microarthropods, nematodes, fluff-grass (Dasyochloa pulchella) growth, and root nitrogen in samples from study plots sampled approximately monthly between May 1986 and August 1987 at the Jornada Basin LTER site in southern New Mexico USA. The purpose of this study was to test how watering, and changing densities of soil microarthropods and nematodes, results in changes in fluff grass growth and root nitrogen. Twenty 6 x 6 m plots were established with a 3 m buffer between plots. Five plots were randomly assigned to one of four treatments: 1) Chlordane to exclude microarthropods, 2) Chlordane and water, 3) Water, and 4) Control. At monthly intervals, randomly selected fluff grass plants were collected from each plot. This data set consists of plant diameters (cm), mite soil weight (g), root weight (g), nematode soil weight (g), root total nitrogen (mg/g), and nematode number. This study was completed in November 1987.
Gopher-disturbed and undisturbed soil Oribatid mite data for Martinelli slope, 1988.
Soil cores were collected from undisturbed and pocket gopher (Thomomys talpoides) disturbed alpine tundra. Cores were split in half longitudinally with one half being used for extraction and identification of Oribatid mites. Disturbed soils included both old and fresh gopher mounds and all study sites were located on the Martinelli slope directly above the 25 permanent plots. The cores were collected in 1988.
Figure 3 in Two new genera, Limnohalacarus and Soldanellonyx (Acari: Halacaridae) in freshwater halacarid mites with additional new records from Turkey
Figure 3. Halacarellus hyrcanus (Viets, 1928) (deutonymph) – A. Idiosoma, dorsal view; B. Idiosoma, ventral view; C. Gnathosoma, ventral view; D. Leg I, medial view; E. H. hyrcanus (protonymph) – E idiosoma, ventral view. Scale bars: A–C 100 µm, D–E 50 µm.
Figure 6. Soldanellonyx monardi Walter, 1919 in Two new genera, Limnohalacarus and Soldanellonyx (Acari: Halacaridae) in freshwater halacarid mites with additional new records from Turkey
Figure 6. Soldanellonyx monardi Walter, 1919 (female) – A. idiosoma, dorsal view; B. idiosoma, ventral view; C. gnathosoma, ventral view and chelicera, lateral view; D. palp, medial view; E. leg I, lateral view; F. Genitoanal plate, deutonymph; G–H. Porohalacarus alpinus (Thor, 1910), deutonymph; G. idiosoma, dorsal view; H. Genitoanal plate. Scale bars: 50 µm.
Figure 4 in Two new genera, Limnohalacarus and Soldanellonyx (Acari: Halacaridae) in freshwater halacarid mites with additional new records from Turkey
Figure 4. Limnohalacarus wackeri (Walter, 1914) (male) – A. Idiosoma, dorsal view; B idiosoma, ventral view; C. reticulation on the plates; D. Gnathosoma, ventral view; E. Palp, lateral view; F. Leg I, medial view. Scale bars: 100 µm.
Fig. 5 in Contributions to the knowledge of the mite genus Stigmaeus Koch, 1836 (Acari: Stigmaeidae) of Turkey
Fig. 5. Stigmaeus miandoabiensis Bagheri & Zarei, 2012. A. Some dorsal body setae. B. Palp (♀). Scale bars = 40 μm.
Fig. 1 in Contributions to the knowledge of the mite genus Stigmaeus Koch, 1836 (Acari: Stigmaeidae) of Turkey
Fig. 1. Stigmaeus bifurcus sp. nov. A–B. Holotype (♀). A. Dorsum of body. B. Venter of body. – C–D. Paratype (♀). C. Abnormality: left seta c1 about 2 times as long as the right. D. Abnormality: seta h3 absent on right suranal shield in one paratype. Scale bars = 100 μm.
Fig. 2 in Contributions to the knowledge of the mite genus Stigmaeus Koch, 1836 (Acari: Stigmaeidae) of Turkey
Fig. 2. Stigmaeus bifurcus sp. nov., holotype, ♀. A. Some dorsal body setae. B. Palp. C. Leg I. D. Leg II. E. Leg III. F. Leg IV. Scale bars: A–B = 40 μm; C–F = 100 μm.
Fig. 5 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 5. Neophyllobius tepoztlanensis sp. nov., ♀, holotype. A. Palp. B. Subcapitulum. C. Dorsal idiosoma. D. Ventral idiosoma. E. Trochanter–tibia of leg I. F. Tarsus I.
Fig. 4 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 4. Schematic tarsal setations of Neophyllobius cibyci sp. nov. A–D. ♀, holotype. A. Tarsus I. B. Tarsus II. C. Tarsus III. D. Tarsus IV. E–H. ♁, paratype (CNAC009238). E. Tarsus I. F. Tarsus II. G. Tarsus III. H. Tarsus IV. I–L. Protonymph, paratype (CNAC009241). I. Tarsus I. J. Tarsus II. K. Tarsus III. L. Tarsus IV. M–O. Larva, paratype (CNAC009242). M. Tarsus I. N. Tarsus II. O. Tarsus III.
Fig. 1 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 1. Neophyllobius cibyci sp. nov., ♀, holotype. A. Palp. B. Subcapitulum. C. Dorsal idiosoma. D. Ventral idiosoma. E. Trochanter–tibia of leg I. F. Tarsus I.
Fig. 2 in Camerobiid mites (Acariformes: Raphignathina: Camerobiidae) inhabiting epiphytic bromeliads and soil litter of tropical dry forest with analysis of setal homology in the genus Neophyllobius
Fig. 2. Neophyllobius cibyci sp. nov. A–B. ♁, paratype (CNAC009238). A. Dorsal idiosoma. B. Ventral idiosoma. C–D. Protonymph, paratype (CNAC009241). C. Dorsal idiosoma. D. Ventral idiosoma. E–F. Larva, paratype (CNAC009242). E. Dorsal idiosoma. F. Ventral idiosoma.
Figure 8 in Ultrastructure of the prosomal gland complex in unfed larvae of the fresh-water mite Limnesia maculata (Müller, 1776) (Acariformes, Limnesiidae)
Figure 8 Organization of the labyrinth of coxal glands in unfed larvaeL. maculata.TEM. a – Central portion of the labyrinth with a conspicuous central lumen filled with various membranous and granular structures. Scale bar – 2 μm; b – Portion of the labyrinth with a collapsed lumen penetrated by microvilli. Scale bar – 2 μm; c – Basal lamina penetrating between the gland cells at their base (arrow). Scale bar – 0.5µζ; d – Portion of the convoluted labyrinth showing semi-circled mutual invagination of the gland cells (arrow). Scale bar – 1 μm; e – The apical cell contact with hardly distinguishable septate junction (arrow). Note axial filaments within microvilli (arrowheads). Scale bar – 0.5 μm. gl – glycogen; gll – gland lumen; m – mitochondria; mg – midgut; mt – microtubules; mv – microvilli; n – nucleus; nu – nucleolus; rb – residual body; rer – rough endoplasmic reticulum.
Figure 1 in Ultrastructure of the prosomal gland complex in unfed larvae of the fresh-water mite Limnesia maculata (Müller, 1776) (Acariformes, Limnesiidae)
Figure 1 Podocephalic glands in unfed larvaeL. maculatain sagittal sections. TEM. a – Nearly axial section showing two medial glands located one after another as well as pharynx and chelicera. Scale bar – 20 μm; b – Section slightly apart from the axial line showing medial glands and podocephalic canal.Arrow indicates long extensions of the duct-forming cells flanking lateral lacunas of the intra-alveolar lumen. Scale bar – 10 μm; c – Section through the region of the origin of leg I showing the lateral and the ventral glands as well as the terminal bladder of the coxal gland in a nearly collapsed condition. Scale bar – 20 μm. amg – anterior medial gland; bl – bladder; br – brain; ch – chelicera; hem – hemocyte; ial – intra-alveolar lumen; lg – lateral gland; legI – leg I; ms – muscles; pc – podocephalic canal; ph – pharynx; pmg – posterior medial gland; schs – subcheliceral space; vg – ventral gland.
Figure 1 in Functional response of the predatory mite Amblyseius swirskii (Acari: Phytoseiidae) to Eotetranychus frosti (Tetranychidae) and Cenopalpus irani (Tenuipalpidae)
Figure 1 Functional response curves of adult female Amblyseius swirskii to different stages of Eotetranychus frosti and Cenopalpus irani. Dots represent the observed numbers of prey consumed at each initial prey density, and lines were predicted by the random predator equation (Rogers, 1972).
Figure 5 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic
Figure 5. Coxigenital region of Aceria rhodiolae females from (A) Russia, and (B,C,E) Nunavik, Canada. (A,B) Differential interference contrast light microscopy, (C,E) scanning electron micrograph, (D) line drawing. Scale on (B) also applies to (A). Notations on (D) indicate palp, leg and idiosomal setae, and coxal apodemes (ap1, ap2, ap; pra, prosternal apodeme). Other arrows elsewhere indicate characteristic ridges on coxal plates (a,b,c); genital flange (fl), and underlying postgenital plate (pp), which bears setae 3a and extends anterolaterally into lateral flaps (f) that flank the genital coverflap; and ventral ridges on femur, genu, and coxal fields (E).
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