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875 results for “Infestation”
Fig. 7 in Efficacy Of Protein Bait Sprays In Controlling Fruit Flies (Diptera: Tephritidae) Infesting Angled Luffa And Bitter Gourd In Thailand
Fig. 7. Number and sex ratio of fruit fly collected from funnel traps in angled luffa plot treated with Pinnacle bait.
Fig. 2 in Efficacy Of Protein Bait Sprays In Controlling Fruit Flies (Diptera: Tephritidae) Infesting Angled Luffa And Bitter Gourd In Thailand
Fig. 2. Number of fruit flies collected from fallen flowers of angled luffa in plots treated with Pinnacle bait and untreated. (Only Bactrocera diversa was found.)
Fig. 1 in Lice community structure infesting Trinomys iheringi (Thomas, 1911) - Ocurrence, sex bias and climatic variables on tropical island
Fig. 1. Location of capture of Trinomys iheringi in Dois Rios Village, Ilha Grande, Rio de Janeiro State, Brazil, between April 2013, and December 2015.
Fig. 2 in First record of an aquatic oligochaete infesting fish
Fig. 2. Pristina aequiseta between gill filaments of Murray cod. (a) Low magnification showing gill filaments (Gf) and oligochaete (Ol). (b) Anterior end showing distinctive proboscis (Pb) and segments with setae (Se).
Fig. 2 in Lice community structure infesting Trinomys iheringi (Thomas, 1911) - Ocurrence, sex bias and climatic variables on tropical island
Fig. 2. Distribution of Gyropus (m.) martini stages on Trinomys iheringi rodents. Host sex (F = female, M = male) and capture months (Aug = August, Dec = December, Feb = February, Jul = July, Nov = November) in Ilha Grande State Park, RJ, Brazil. The numbers along the x axis represent the number of lice life stages: male/female/nymph 1/nymph 2/nymph 3.
Fig. 4 in Lice community structure infesting Trinomys iheringi (Thomas, 1911) - Ocurrence, sex bias and climatic variables on tropical island
Fig. 4. Probability of lice occurrence on Trinomys iheringi as a function of humidity and sex (A), and humidity and age class (B) in Ilha Grande State Park, RJ, Brazil. The letters in the upper part of the graph represent the presence of lice on rodents, and the letters in the lower part of the graph indicate the absence of lice on rodents.
Fig. 3 in Lice community structure infesting Trinomys iheringi (Thomas, 1911) - Ocurrence, sex bias and climatic variables on tropical island
Fig. 3. Relationship between the natural logarithm of body mass and the natural logarithm of body length for Trinomys iheringi individuals infected and uninfected by lice in Ilha Grande State Park, RJ, Brazil. Open circles and the continuous line refer to uninfected individuals, while solid circles and the dashed line refer to infected individuals.
Fig. 1 in First record of an aquatic oligochaete infesting fish
Fig. 1. Fish mortality rate (fish/tank/day) for 16 tanks in a Murray cod recirculating aquaculture system infested with Pristina aequiseta (values represent mean and standard error).
Fig. 1 in Ecology of bat flies in Singapore: A study on the diversity, infestation bias and host specificity (Diptera: Nycteribiidae)
Fig. 1. Pteropodid fruit bats in Singapore with their ectoparasitic Nycteribiidae bat flies. Cynopterus brachyotis (a) and Leptocyclopodia ferrarii (b); Eonycteris spelaea (c) and Eucampsipoda sundaica (d); Penthetor lucasi (e), Eucampsipoda penthetoris (f), and Archinycteribia octophthalma (g).
Fig. 2 in Ecology of bat flies in Singapore: A study on the diversity, infestation bias and host specificity (Diptera: Nycteribiidae)
Fig. 2. Posterior mean intensity of the three species of bats and 89% HDPI (High Density Posterior Interval).
Fig. 1 in New records of mealybugs (Hemiptera: Pseudococcidae) infesting rosettes of Conilon coffee plants in the state of Rondônia, South-Western Amazon, Brazil
Fig. 1. Ferrisia dasylirii and Planococcus minor in rosettes of Conilon coffee trees in the state of Rondônia, South-Western Amazon, Brazil. (A-B) Colonies of F. dasylirii on peduncles of coffee fruits. (C) Fruits covered by sooty mold on top of F. dasylirii honeydew. (D) Branch with damage (scattered grain) of F. dasylirii. (E) Dorsal view of an F. dasylirii adult female. (F) Imatures and adult females of P. minor. Photos (A-C) and (E-F) Rondelli VM; (D) Dias JRM.
Fig. 2 in Can the environment influence varroosis infestation in Africanized honey bees in a Neotropical region?
Fig. 2. Biplot of canonical discriminator of temperature (°C), rainfall (mm), altitude (m), and Varroa destructor infestation level (%) from Bahia State mesoregions, Brazil. BA1: São Francisco Valley; BA2: Middle East; BA3: Metropolitan of Salvador; BA4: South Center; BA5: South.
Fig. 1 in Can the environment influence varroosis infestation in Africanized honey bees in a Neotropical region?
Fig. 1. Cities (black squares) where the apiaries are located from 5 different mesoregions in Bahia State, Brazil. BA1: São Francisco Valley; BA2: Middle East; BA3: Metropolitan of Salvador; BA4: South Center; BA5: South.
Fig. 3. A in Differential proteomic analysis of date palm leaves infested with the red palm weevil (Coleoptera: Curculionidae)
Fig. 3. A pie chart presenting the classification of identified proteins according to their biological functions, expressed in percentage.
Fig. 1 in Differential proteomic analysis of date palm leaves infested with the red palm weevil (Coleoptera: Curculionidae)
Fig. 1. Two-dimensional differential gel electrophoresis representative images of date palm proteins. The protein sample of control, wounded, infested, and internal standard (pooled of all the samples) are individually labeled with Cy dyes, mixed together and separated by two-dimensional differential gel electrophoresis followed by image scanning. (A) image of date palm control sample and labeled with cy3 dye; (B) image of date palm artificially wounded sample labeled with cy5 dye; (C) image of date palm sample infested with red palm weevil and labeled with cy3 dye; (D) image of date palm sample pooled from all and labeled with cy2 dye; (E) overlay gel of control, infested, and wounded along with internal standard.
Fig. 2 in Differential proteomic analysis of date palm leaves infested with the red palm weevil (Coleoptera: Curculionidae)
Fig. 2. Venn diagram for the relative distribution of proteins spots in control, mechanically wounded, and red palm weevil infested date palm samples. The non-overlapping segment of diagram represent the number of proteins which were significantly up-regulated (> 1.5-fold) in the corresponding group when compared with the other two groups. The overlapping region between any two groups represents the number of protein spots significantly up-regulated (> 1.5-fold) compared to the third one. The central overlapping region depicts the protein spots where no statistically significant change in up- or down-regulation was observed.
Fig. 3 in Can the environment influence varroosis infestation in Africanized honey bees in a Neotropical region?
Fig. 3. Contribution of the variables in the first canonical discriminant function from temperature (°C), rainfall (mm), altitude (m), and Varroa destructor infestation level (%) from 5 different mesoregions in Bahia State,Brazil.BA1: São Francisco Valley; BA2: Middle East; BA3: Metropolitan of Salvador; BA4: South Center; BA5: South.
Fig. 3 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 3. Number of infested fruits and presence of weevil larvae in different jalapeño plant parts (means ± SE). Number of infested fruits in 5 directions (A), in 3 layers (C), and at 5 spacings (E). Number of larval A. eugenii within infested fruits in 5 directions (B), in 3 layers (D), and at 5 spacings (F). Different letters indicate significant differences among the treatments (means separated by Tukey's HSD, P <0.05).
Fig. 4 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 4. Fruit wall thickness and single weight in different jalapeño plant parts (means ± SE). Fruit wall thickness (A) and single weight (B) in 5 directions, fruit wall thickness (C) and single weight (D) in 3 layers, fruit wall thickness (E) and single weight (F) at 5 spacings. Different letters indicate significant differences among the treatments (means separated by Tukey's HSD, P <0.05).
Fig. 1 in Spread of two invasive flies (Diptera: Drosophilidae) infesting commercial fruits in southeastern Brazil
Fig. 1. Brazilian states previously invaded by Drosophila suzukii and its new dispersion area in Espírito Santo State, Brazil.
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