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Tetranychus evansi spider mite populations suppress tomato defenses to varying degrees

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9781118829783.ch3openalex-snapshot
Insect Detoxification and Sequestration Strategies
inferredcites →https://doi.org/10.1002/bimj.200810425openalex-snapshot
Simultaneous Inference in General Parametric Models
inferredcites →https://doi.org/10.1002/ece3.6204openalex-snapshot
Tetranychus evansi spider mite populations suppress tomato defenses to varying degrees
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02730.xopenalex-snapshot
GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
inferredcites →https://doi.org/10.1002/ps.4100openalex-snapshot
Steroidal glycoalkaloids: chemical defence of edible African nightshades against the tomato red spider mite, Tetranychus evansi (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1007/978-1-4020-8182-8_12openalex-snapshot
Defensive Roles of Polyphenol Oxidase in Plants
inferredcites →https://doi.org/10.1007/978-90-481-9837-5_96openalex-snapshot
Spider Mites Web: A comprehensive database for the Tetranychidae
inferredcites →https://doi.org/10.1007/bf00020894openalex-snapshot
Induction of tomato stress protein mRNAs by ethephon, 2,6-dichloroisonicotinic acid and salicylate
inferredcites →https://doi.org/10.1007/bf00023601openalex-snapshot
Organisation of the tomato polyphenol oxidase gene family
inferredcites →https://doi.org/10.1007/bf00040610openalex-snapshot
Differential accumulation of mRNAs encoding extracellular and intracellular PR proteins in tomato induced by virulent and avirulent races of Cladosporium fulvum
inferredcites →https://doi.org/10.1007/bf00232123openalex-snapshot
Intrinsic GUS-like activities in seed plants
inferredcites →https://doi.org/10.1007/bf02854036openalex-snapshot
Glycoalkaloids as pest resistance factors
inferredcites →https://doi.org/10.1007/s00265-016-2124-0openalex-snapshot
Incomplete species recognition entails few costs in spider mites, despite first-male precedence
inferredcites →https://doi.org/10.1007/s003440000026openalex-snapshot
The Myriad Plant Responses to Herbivores
inferredcites →https://doi.org/10.1007/s00442-015-3344-0openalex-snapshot
Herbivores with similar feeding modes interact through the induction of different plant responses
inferredcites →https://doi.org/10.1007/s00442-015-3434-zopenalex-snapshot
Down-regulation of plant defence in a resident spider mite species and its effect upon con- and heterospecifics
inferredcites →https://doi.org/10.1007/s00442-015-3508-yopenalex-snapshot
Intraspecific differences in plant chemotype determine the structure of arthropod food webs
inferredcites →https://doi.org/10.1007/s10340-017-0852-1openalex-snapshot
Host plant use by two distinct lineages of the tomato red spider mite, Tetranychus evansi, differing in their distribution range
inferredcites →https://doi.org/10.1007/s10493-010-9344-1openalex-snapshot
Spider mite web mediates anti-predator behaviour
inferredcites →https://doi.org/10.1007/s10493-010-9362-zopenalex-snapshot
Reproductive performance of seven strains of the tomato red spider mite Tetranychus evansi (Acari: Tetranychidae) at five temperatures
inferredcites →https://doi.org/10.1007/s10493-012-9590-5openalex-snapshot
Review of the invasion of Tetranychus evansi: biology, colonization pathways, potential expansion and prospects for biological control
inferredcites →https://doi.org/10.1007/s10493-012-9645-7openalex-snapshot
The invasive spider mite Tetranychus evansi (Acari: Tetranychidae) alters community composition and host-plant use of native relatives
inferredcites →https://doi.org/10.1007/s10493-015-9985-1openalex-snapshot
Why do males choose heterospecific females in the red spider mite?
inferredcites →https://doi.org/10.1007/s10530-015-0873-8openalex-snapshot
Genetic traits leading to invasion: plasticity in cold hardiness explains current distribution of an invasive agricultural pest, Tetranychus evansi (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1007/s10886-005-4244-2openalex-snapshot
Herbivore-induced Plant Volatiles Trigger Sporulation in Entomopathogenic Fungi: The Case of Neozygites tanajoae Infecting the Cassava Green Mite
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Inhibition of Proteinase Inhibitor Transcripts by Leptinotarsa decemlineata Regurgitant in Solanum lycopersicum
inferredcites →https://doi.org/10.1007/s11418-006-0021-yopenalex-snapshot
Physiological functions of solanaceous and tomato steroidal glycosides
inferredcites →https://doi.org/10.1016/j.ab.2009.01.024openalex-snapshot
Reference gene selection for quantitative real-time PCR normalization in tomato subjected to nitrogen, cold, and light stress
inferredcites →https://doi.org/10.1016/j.baae.2010.03.003openalex-snapshot
Vegetation complexity—The influence of plant species diversity and plant structures on plant chemical complexity and arthropods
inferredcites →https://doi.org/10.1016/j.jip.2009.08.012openalex-snapshot
Host range of Neozygites floridana isolates (Zygomycetes: Entomophthorales) to spider mites
inferredcites →https://doi.org/10.1016/j.jplph.2005.10.014openalex-snapshot
The wound response in tomato – Role of jasmonic acid
inferredcites →https://doi.org/10.1016/j.plantsci.2016.08.004openalex-snapshot
Induced plant-defenses suppress herbivore reproduction but also constrain predation of their offspring
inferredcites →https://doi.org/10.1016/j.tplants.2008.08.003openalex-snapshot
Consequences of variation in plant defense for biodiversity at higher trophic levels
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.010openalex-snapshot
Evolution of jasmonate and salicylate signal crosstalk
inferredcites →https://doi.org/10.1016/j.tree.2007.07.009openalex-snapshot
The tragedy of the commons in evolutionary biology
inferredcites →https://doi.org/10.1016/s0015-3796(80)80059-xopenalex-snapshot
„Die Senfolbombe“: Zur Kompartimentierung des Myrosinasesystems
inferredcites →https://doi.org/10.1016/s0031-9422(03)00300-5openalex-snapshot
Evolution of secondary metabolites from an ecological and molecular phylogenetic perspective
inferredcites →https://doi.org/10.1023/a:1006144610009openalex-snapshot
The effect of temperature on life history parameters of Tetranychus evansi (Acari: Tetranychidae)
inferredcites →https://doi.org/10.1023/b:joec.0000008010.40606.b0openalex-snapshot
Induction of Direct and Indirect Plant Responses by Jasmonic Acid, Low Spider Mite Densities, or a Combination of Jasmonic Acid Treatment and Spider Mite Infestation
inferredcites →https://doi.org/10.1038/35037572openalex-snapshot
The population genetics of ecological specialization in evolving Escherichia coli populations
inferredcites →https://doi.org/10.1038/416599aopenalex-snapshot
Caterpillar saliva beats plant defences
inferredcites →https://doi.org/10.1038/hdy.2014.53openalex-snapshot
Testing for reproductive interference in the population dynamics of two congeneric species of herbivorous mites
inferredcites →https://doi.org/10.1038/hdy.2016.103openalex-snapshot
Detection of genetic incompatibilities in non-model systems using simple genetic markers: hybrid breakdown in the haplodiploid spider mite Tetranychus evansi
inferredcites →https://doi.org/10.1038/nature11119openalex-snapshot
The tomato genome sequence provides insights into fleshy fruit evolution
inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot
jModelTest 2: more models, new heuristics and parallel computing
inferredcites →https://doi.org/10.1046/j.1461-0248.2000.00137.xopenalex-snapshot
Can plants use entomopathogens as bodyguards?
inferredcites →https://doi.org/10.1073/pnas.0802224105openalex-snapshot
Mitochondrial heteroplasmy and the evolution of insecticide resistance: Non-Mendelian inheritance in action
inferredcites →https://doi.org/10.1073/pnas.1213214110openalex-snapshot
A link between host plant adaptation and pesticide resistance in the polyphagous spider mite Tetranychus urticae
inferredcites →https://doi.org/10.1073/pnas.1504977112openalex-snapshot
Phytochemical diversity drives plant–insect community diversity
inferredcites →https://doi.org/10.1074/mcp.m116.058081openalex-snapshot
The Salivary Protein Repertoire of the Polyphagous Spider Mite Tetranychus urticae: A Quest for Effectors
inferredcites →https://doi.org/10.1080/01647950903431156openalex-snapshot
Evidence of co-specificity betweenTetranychus evansiandTetranychus takafujii(Acari: Prostigmata, Tetranychidae): comments on taxonomic and agricultural aspects
inferredcites →https://doi.org/10.1080/15592324.2017.1370526openalex-snapshot
Spatiotemporal heterogeneity of tomato induced defense responses affects spider mite performance and behavior
inferredcites →https://doi.org/10.1080/17429145.2010.551670openalex-snapshot
Avoidance and suppression of plant defenses by herbivores and pathogens
inferredcites →https://doi.org/10.1086/286069openalex-snapshot
Secondary Metabolites Of Fleshy Vertebrate‐Dispersed Fruits: Adaptive Hypotheses And Implications For Seed Dispersal
inferredcites →https://doi.org/10.1086/420980openalex-snapshot
Plant Defense and Density Dependence in the Population Growth of Herbivores
inferredcites →https://doi.org/10.1086/511529openalex-snapshot
Community heterogeneity and the evolution of interactions between plants and insect herbivores
inferredcites →https://doi.org/10.1093/aob/mcv054openalex-snapshot
Mechanisms and ecological consequences of plant defence induction and suppression in herbivore communities
inferredcites →https://doi.org/10.1093/beheco/arx161openalex-snapshot
Despite reproductive interference, the net outcome of reproductive interactions among spider mite species is not necessarily costly
inferredcites →https://doi.org/10.1093/molbev/mst012openalex-snapshot
Building Phylogenetic Trees from Molecular Data with MEGA
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/nar/17.6.2362openalex-snapshot
A small-scale procedure for the rapid isolation of plant RNAs
inferredcites →https://doi.org/10.1093/nar/21.20.4850openalex-snapshot
Rapid purification of high-activityTaqDNA polymerase
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkp045openalex-snapshot
Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029397openalex-snapshot
Antagonistic Effect of Salicylic Acid and Jasmonic Acid on the Expression of Pathogenesis-Related (PR) Protein Genes in Wounded Mature Tobacco Leaves
inferredcites →https://doi.org/10.1094/mpmi-09-14-0291-fiopenalex-snapshot
Tomato Whole Genome Transcriptional Response toTetranychus urticaeIdentifies Divergence of Spider Mite-Induced Responses Between Tomato andArabidopsis
inferredcites →https://doi.org/10.1094/mpmi-9-0409openalex-snapshot
Characterization of Defense-Related Genes Ectopically Expressed in Viroid-lnfected Tomato Plants
inferredcites →https://doi.org/10.1098/rspb.1979.0081openalex-snapshot
Arms races between and within species
inferredcites →https://doi.org/10.1098/rspb.2007.1277openalex-snapshot
Intraspecific variation in a generalist herbivore accounts for differential induction and impact of host plant defences
inferredcites →https://doi.org/10.1104/pp.005314openalex-snapshot
Resistance of Cultivated Tomato to Cell Content-Feeding Herbivores Is Regulated by the Octadecanoid-Signaling Pathway
inferredcites →https://doi.org/10.1104/pp.103.038315openalex-snapshot
Differential Timing of Spider Mite-Induced Direct and Indirect Defenses in Tomato Plants
inferredcites →https://doi.org/10.1104/pp.104.048694openalex-snapshot
Jasmonic Acid Is a Key Regulator of Spider Mite-Induced Volatile Terpenoid and Methyl Salicylate Emission in Tomato
inferredcites →https://doi.org/10.1104/pp.106.090035openalex-snapshot
Silverleaf Whitefly Induces Salicylic Acid Defenses and Suppresses Effectual Jasmonic Acid Defenses
inferredcites →https://doi.org/10.1104/pp.110.4.1257openalex-snapshot
A Complex Array of Proteins Related to the Multimeric Leucine Aminopeptidase of Tomato
inferredcites →https://doi.org/10.1104/pp.120.4.979openalex-snapshot
Leucine Aminopeptidase RNAs, Proteins, and Activities Increase in Response to Water Deficit, Salinity, and the Wound Signals Systemin, Methyl Jasmonate, and Abscisic Acid1
inferredcites →https://doi.org/10.1105/tpc.017954openalex-snapshot
The Tomato Homolog of CORONATINE-INSENSITIVE1 Is Required for the Maternal Control of Seed Maturation, Jasmonate-Signaled Defense Responses, and Glandular Trichome Development[W]
inferredcites →https://doi.org/10.1105/tpc.104.029736openalex-snapshot
Metabolic, Genomic, and Biochemical Analyses of Glandular Trichomes from the Wild Tomato SpeciesLycopersicon hirsutumIdentify a Key Enzyme in the Biosynthesis of Methylketones
inferredcites →https://doi.org/10.1105/tpc.108.065029openalex-snapshot
Leucine Aminopeptidase Regulates Defense and Wound Signaling in Tomato Downstream of Jasmonic Acid
inferredcites →https://doi.org/10.1105/tpc.109.073395openalex-snapshot
Serine Protease Inhibitors Specifically Defend Solanum nigrum against Generalist Herbivores but Do Not Influence Plant Growth and Development
inferredcites →https://doi.org/10.1105/tpc.12.8.1409openalex-snapshot
Local and Systemic Changes in Squash Gene Expression in Response to Silverleaf Whitefly Feeding
inferredcites →https://doi.org/10.1111/j.1095-8312.1984.tb00145.xopenalex-snapshot
Enemy free space and the structure of ecological communities
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02749.xopenalex-snapshot
A genetic similarity rule determines arthropod community structure
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02842.xopenalex-snapshot
Ethylene‐induced stomatal closure in Arabidopsis occurs via AtrbohF‐mediated hydrogen peroxide synthesis
inferredcites →https://doi.org/10.1111/j.1461-0248.2004.00616.xopenalex-snapshot
Is invasion success explained by the enemy release hypothesis?
inferredcites →https://doi.org/10.1111/j.1461-0248.2010.01575.xopenalex-snapshot
A herbivore that manipulates plant defence
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DETOXICATION MECHANISMS IN INSECTS
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A multicomponent, elicitor‐inducible cystatin complex in tomato, Solanum lycopersicum
inferredcites →https://doi.org/10.1111/j.1570-7458.2007.00587.xopenalex-snapshot
Use of odours by Cycloneda sanguinea to assess patch quality
inferredcites →https://doi.org/10.1111/j.1600-0587.1999.tb00504.xopenalex-snapshot
Geographic variation and evolution of immunosuppressive genes in a Drosophila parasitoid
inferredcites →https://doi.org/10.1111/mec.13330openalex-snapshot
Adaptation of a polyphagous herbivore to a novel host plant extensively shapes the transcriptome of herbivore and host
inferredcites →https://doi.org/10.1111/nph.12977openalex-snapshot
Herbivore‐induced plant volatiles: targets, perception and unanswered questions
inferredcites →https://doi.org/10.1111/nph.13075openalex-snapshot
Spider mites suppress tomato defenses downstream of jasmonate and salicylate independently of hormonal crosstalk
inferredcites →https://doi.org/10.1111/nph.14038openalex-snapshot
Intraspecific phytochemical variation shapes community and population structure for specialist caterpillars
inferredcites →https://doi.org/10.1111/nph.14543openalex-snapshot
Overcompensation of herbivore reproduction through hyper‐suppression of plant defenses in response to competition
inferredcites →https://doi.org/10.1111/tpj.13152openalex-snapshot
Salivary proteins of spider mites suppress defenses in Nicotiana benthamiana and promote mite reproduction
inferredcites →https://doi.org/10.1126/science.221.4607.277openalex-snapshot
Rapid Changes in Tree Leaf Chemistry Induced by Damage: Evidence for Communication Between Plants
inferredcites →https://doi.org/10.1146/annurev.earth.26.1.329openalex-snapshot
EARLY HISTORY OF ARTHROPOD AND VASCULAR PLANT ASSOCIATIONS
inferredcites →https://doi.org/10.1146/annurev.ecolsys.39.110707.173437openalex-snapshot
Spontaneous Mutation Accumulation Studies in Evolutionary Genetics
inferredcites →https://doi.org/10.1186/1471-2148-9-182openalex-snapshot
Are adaptation costs necessary to build up a local adaptation pattern?
inferredcites →https://doi.org/10.1186/s12915-014-0098-9openalex-snapshot
Defense suppression benefits herbivores that have a monopoly on their feeding site but can backfire within natural communities
inferredcites →https://doi.org/10.1303/aez.2003.109openalex-snapshot
A comparison of the responses of Tetranychus urticae (Acari:Tetranychidae) and Phytoseiulus persimilis (Acari: Phytoseiidae) to volatiles emitted from lima bean leaves with different levels of damage made by T. urticae or Spodoptera exigua (Lepidoptera: Noctuidae).
inferredcites →https://doi.org/10.1371/journal.pone.0001021openalex-snapshot
Maladaptation and the Paradox of Robustness in Evolution
inferredcites →https://doi.org/10.1371/journal.pone.0023757openalex-snapshot
A Herbivorous Mite Down-Regulates Plant Defence and Produces Web to Exclude Competitors
inferredcites →https://doi.org/10.1371/journal.pone.0035601openalex-snapshot
Test of Colonisation Scenarios Reveals Complex Invasion History of the Red Tomato Spider Mite Tetranychus evansi
inferredcites →https://doi.org/10.1371/journal.pone.0043011openalex-snapshot
Gene Pyramiding of Peptidase Inhibitors Enhances Plant Resistance to the Spider Mite Tetranychus urticae
inferredcites →https://doi.org/10.1371/journal.pone.0066445openalex-snapshot
Uncertainties in Predicting Species Distributions under Climate Change: A Case Study Using Tetranychus evansi (Acari: Tetranychidae), a Widespread Agricultural Pest
inferredcites →https://doi.org/10.1590/s1519-566x2010000600022openalex-snapshot
Efficiency of Phytoseiulus longipes Evans as a control agent of Tetranychus evansi Baker & Pritchard (Acari: Phytoseiidae: Tetranychidae) on screenhouse tomatoes
inferredcites →https://doi.org/10.1673/031.010.4201openalex-snapshot
Determination of pH in Regions of the Midguts of Acaridid Mites
inferredcites →https://doi.org/10.18637/jss.v059.i09openalex-snapshot
A Kenward-Roger Approximation and Parametric Bootstrap Methods for Tests in Linear Mixed Models - The R Package pbkrtest
inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.2307/25065301openalex-snapshot
Comparison of AFLPs with other markers for phylogenetic inference in wild tomatoes [ Solanum L. section Lycopersicon (Mill.) Wettst.]
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3389/fpls.2013.00262openalex-snapshot
Quantitative patterns between plant volatile emissions induced by biotic stresses and the degree of damage
inferredcites →https://doi.org/10.3389/fpls.2016.01105openalex-snapshot
Plant-Herbivore Interaction: Dissection of the Cellular Pattern of Tetranychus urticae Feeding on the Host Plant
inferredcites →https://doi.org/10.3389/fpls.2018.00986openalex-snapshot
Arabidopsis Kunitz Trypsin Inhibitors in Defense Against Spider Mites
inferredcites →https://doi.org/10.3389/fpls.2018.01057openalex-snapshot
Why Do Herbivorous Mites Suppress Plant Defenses?
inferredcites →https://doi.org/10.3390/ijms18010182openalex-snapshot
Independent Effects of a Herbivore’s Bacterial Symbionts on Its Performance and Induced Plant Defences
inferredcites →https://doi.org/10.3390/ijms19103265openalex-snapshot
Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites
inferredcites →https://doi.org/10.4241/kyubyochu.55.136openalex-snapshot
Occurrence of the spider mite Tetranychus takafujii Ehara & Ohashi in Kyushu and Okinawa.
inferredcites →https://doi.org/10.5061/dryad.np5hqbzpwopenalex-snapshot
Data from: Tetranychus evansi spider mite populations suppress tomato defences to varying degrees

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.24349/78jc-6nevzenodo-depositor-declared
First record of the tomato red spider mite, Tetranychus evansi Baker and Pritchard (Acari: Tetranychidae) in Mexico, from cultivated and wild solanaceous plants
inferred← citeshttps://doi.org/10.1002/ece3.71706openalex-snapshot
Suppression of Plant Resistance May Be a Common Trait Among Adapted Herbivores
inferred← citeshttps://doi.org/10.1007/s00442-023-05359-0openalex-snapshot
Imperfect diet choice reduces the performance of a predatory mite
inferred← citeshttps://doi.org/10.1007/s10340-022-01516-1openalex-snapshot
Plant defences and spider-mite web affect host plant choice and performance of the whitefly Bemisia tabaci
inferred← citeshttps://doi.org/10.1007/s10886-023-01455-wopenalex-snapshot
Plant Variety, Mycorrhization, and Herbivory Influence Induced Volatile Emissions and Plant Growth Characteristics in Tomato
inferred← citeshttps://doi.org/10.1007/s12600-024-01154-6openalex-snapshot
Exogenous Methyl Salicylate treatment increases tomato zingiberene levels and decreases infestation of adult whiteflies and red spider mites
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101454openalex-snapshot
Crosstalk between abscisic acid (ABA) and salicylic acid (SA) regulates susceptibility of tomato to the specialist spider mite Tetranychus evansi Baker & Pritchard
inferred← citeshttps://doi.org/10.1093/jee/toae140openalex-snapshot
Current and future invasion risk of tomato red spider mite under climate change
inferred← citeshttps://doi.org/10.1093/jxb/erad452openalex-snapshot
A new spider mite elicitor triggers plant defence and promotes resistance to herbivores
inferred← citeshttps://doi.org/10.1093/jxb/erag357openalex-snapshot
A herbivorous mite protein triggers plant defense and promotes resistance to herbivores
inferred← citeshttps://doi.org/10.1098/rsos.230525openalex-snapshot
Intraspecific variation for host immune activation by the spider mite Tetranychus evansi
inferred← citeshttps://doi.org/10.1101/2024.05.20.594407openalex-snapshot
Competitor Displacement by an Herbivore that Manipulates Plant Defences
inferred← citeshttps://doi.org/10.1101/2024.09.18.613733openalex-snapshot
Tomato spotted wilt virus facilitates non-vector spider mite species ( Tetranychus urticae and Tetranychus evansi ) on whole tomato plants
inferred← citeshttps://doi.org/10.1111/eea.13227openalex-snapshot
Phytophagous mite performance on intact plants and leaf discs with different defence levels
inferred← citeshttps://doi.org/10.19044/esj.2022.v18n33p101openalex-snapshot
Comparative Effects of Some Botanical Extracts and Chemicals in Controlling the Red Spider Mite Tetranychus evansi Baker & Pritchard on Solanaceous Crops
inferred← citeshttps://doi.org/10.20944/preprints202302.0505.v1openalex-snapshot
Tomato Defence Suppression is a Common Trait in Tetranychus urticae Collected from Field-Grown Tomatoes
inferred← citeshttps://doi.org/10.3389/fpls.2025.1645535openalex-snapshot
Red mite (Panonychus citri) attack amplifies citrus rootstock-driven responses in physiological and biochemical traits, VOC emission, and expression of defence-related genes in mandarin scions
inferred← citeshttps://doi.org/10.3390/horticulturae8121217openalex-snapshot
Development of BC3F2 Tomato Genotypes with Arthropod Resistance Introgressed from Solanum habrochaites var. hirsutum (PI127826)
inferred← citeshttps://doi.org/10.3390/plants9091131openalex-snapshot
Early Molecular Responses of Tomato to Combined Moderate Water Stress and Tomato Red Spider Mite Tetranychus evansi Attack
inferred← citeshttps://doi.org/10.3920/29501679-bja10001openalex-snapshot
Tomato spotted wilt virus facilitates non-vector spider mite species (Tetranychus urticae and Tetranychus evansi) on whole tomato plants
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