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Generalist red velvet mite predator (Balaustium sp.) performs better on a mixed diet
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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/bimj.200810425openalex-snapshot
Simultaneous Inference in General Parametric Models
inferredcites →https://doi.org/10.1006/bcon.1995.1038openalex-snapshot
Intraguild Predation Among Biological-Control Agents: Theory and Evidence
inferredcites →https://doi.org/10.1006/jtbi.2002.3029openalex-snapshot
Environmental Variability and Semelparity vs. Iteroparity as Life Histories
inferredcites →https://doi.org/10.1007/1-4020-4767-3_2openalex-snapshot
Intraguild Predation Usually does not Disrupt Biological Control
inferredcites →https://doi.org/10.1007/978-1-4615-2389-5_4openalex-snapshot
Evolution of Life-History Patterns in the Phytoseiidae
inferredcites →https://doi.org/10.1007/978-94-011-3102-5_2openalex-snapshot
Life-history evolution of spider mites
inferredcites →https://doi.org/10.1007/bf00317517openalex-snapshot
Influence of intraguild predation among generalist insect predators on the suppression of an herbivore population
inferredcites →https://doi.org/10.1007/bf00346403openalex-snapshot
The profit of senescence in phytoseiid mites
inferredcites →https://doi.org/10.1007/s00442-001-0846-8openalex-snapshot
The benefits of clustering eggs: the role of egg predation and larval cannibalism in a predatory mite
inferredcites →https://doi.org/10.1007/s00442-006-0527-8openalex-snapshot
Predators induce egg retention in prey
inferredcites →https://doi.org/10.1007/s004420050776openalex-snapshot
Growth, development, and survival of a generalist predator fed single- and mixed-species diets of different quality
inferredcites →https://doi.org/10.1007/s10526-009-9258-1openalex-snapshot
Pest species diversity enhances control of spider mites and whiteflies by a generalist phytoseiid predator
inferredcites →https://doi.org/10.1016/j.biocontrol.2007.10.017openalex-snapshot
Biological control of thrips and whiteflies by a shared predator: Two pests are better than one
inferredcites →https://doi.org/10.1016/j.biocontrol.2008.02.001openalex-snapshot
Grape downy mildew Plasmopara viticola, an alternative food for generalist predatory mites occurring in vineyards
inferredcites →https://doi.org/10.1016/j.biocontrol.2009.09.007openalex-snapshot
Invertebrate biodiversity affects predator fitness and hence potential to control pests in crops
inferredcites →https://doi.org/10.1016/j.biocontrol.2011.02.013openalex-snapshot
Hyperpredation by generalist predatory mites disrupts biological control of aphids by the aphidophagous gall midge Aphidoletes aphidimyza
inferredcites →https://doi.org/10.1016/s0065-308x(08)60074-3openalex-snapshot
Parasitism and Parasitoidism in Tarsonemina (Acari: Heterostigmata) and Evolutionary Considerations
inferredcites →https://doi.org/10.1016/s1572-4379(96)80020-0openalex-snapshot
1.5.3. Evolutionary ecology: Life history patterns, food plant choice and dispersal
inferredcites →https://doi.org/10.1017/cbo9780511542077openalex-snapshot
Theoretical Approaches to Biological Control
inferredcites →https://doi.org/10.1017/cbo9780511542077.009openalex-snapshot
The case for indigenous generalists in biological control
inferredcites →https://doi.org/10.1023/a:1017976725685openalex-snapshot
Phytoseiid predators as potential biological control agents for Bemisia tabaci
inferredcites →https://doi.org/10.1023/a:1021559421344openalex-snapshot
Phytoseiid Predators Suppress Populations of Bemisia Tabaci on Cucumber Plants with Alternative Food
inferredcites →https://doi.org/10.1038/298115a0openalex-snapshot
Big-bang reproduction and ageing in male marsupial mice
inferredcites →https://doi.org/10.1046/j.1365-2311.2002.00456.xopenalex-snapshot
Oviposition patterns in a predatory mite reduce the risk of egg predation caused by prey
inferredcites →https://doi.org/10.1046/j.1420-9101.2001.00322.xopenalex-snapshot
Investment in survival and reproduction along a semelparity–iteroparity gradient in the Beta species complex
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00349.xopenalex-snapshot
Interspecific infanticide deters predators
inferredcites →https://doi.org/10.1078/1439-1791-00031openalex-snapshot
Plants and generalist predators as links between the below-ground and above-ground system
inferredcites →https://doi.org/10.1078/1439-1791-00094openalex-snapshot
Effects of prey type and mixed diets on survival, growth and development of a generalist predator, Pardosa lugubris (Araneae: Lycosidae)
inferredcites →https://doi.org/10.1080/01647954.2011.624123openalex-snapshot
High temperature and dehydration tolerance of the red velvet mite,Balaustiumsp. (Erythraeidae), permit the exploitation of extremely hot, dry microhabitats
inferredcites →https://doi.org/10.1080/01647958108683244openalex-snapshot
Observations on the occurrence and feeding habits ofBalaustium pulmani(Acari: Erythraeidae) in North Carolina apple orchards
inferredcites →https://doi.org/10.1086/282877openalex-snapshot
Life-History Consequences of Natural Selection: Cole's Result Revisited
inferredcites →https://doi.org/10.1086/283798openalex-snapshot
A General Model of Comparative Fecundity for Semelparous and Iteroparous Life Histories
inferredcites →https://doi.org/10.1086/283993openalex-snapshot
Life History Theory and the Equilibrium Status of Populations
inferredcites →https://doi.org/10.1086/284347openalex-snapshot
Biological Control in Theory and Practice
inferredcites →https://doi.org/10.1086/400074openalex-snapshot
The Population Consequences of Life History Phenomena
inferredcites →https://doi.org/10.1086/409052openalex-snapshot
Life-History Tactics: A Review of the Ideas
inferredcites →https://doi.org/10.1093/aesa/63.1.76openalex-snapshot
Life History and Behavior of Balaustium putmani (Acarina: Erythraeidae)1
inferredcites →https://doi.org/10.1093/jee/83.2.384openalex-snapshot
Reproductive Potential, Sex Ratio, and Mating Efficiency of the Straw Itch Mite (Acari: Pyemotidae)
inferredcites →https://doi.org/10.1093/oso/9780195066876.001.0001openalex-snapshot
Applied Demography for Biologists
inferredcites →https://doi.org/10.1093/oso/9780198577416.001.0001openalex-snapshot
The Evolution Of Life Histories
inferredcites →https://doi.org/10.1098/rspb.2005.3127openalex-snapshot
Prey attack and predators defend: counterattacking prey trigger parental care in predators
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00630.xopenalex-snapshot
TO AGE, TO DIE: PARITY, EVOLUTIONARY TRACKING AND COLE'S PARADOX
inferredcites →https://doi.org/10.1111/j.1570-7458.1989.tb02313.xopenalex-snapshot
How larvae of Thrips tabaci reduce the attack success of phytoseiid predators
inferredcites →https://doi.org/10.1111/j.1744-7348.1986.tb03183.xopenalex-snapshot
Predator density manipulation and its effects on populations of Rhopalosiphumpadi (Horn.: Aphididae) in spring barley
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.421openalex-snapshot
HIGHER-ORDER PREDATORS AND THE REGULATION OF INSECT HERBIVORE POPULATIONS
inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145240openalex-snapshot
Can Generalist Predators be Effective Biocontrol Agents?
inferredcites →https://doi.org/10.11646/zootaxa.1079.1.2openalex-snapshot
Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae)
inferredcites →https://doi.org/10.11646/zootaxa.3178.1.1openalex-snapshot
A new species of Balaustium von Heyden, 1826 (Acari: Actinotrichida, Erythraeidae) from Spain
inferredcites →https://doi.org/10.1890/0012-9658(2002)083[2664:hpbfpf]2.0.co;2openalex-snapshot
HOW PLANTS BENEFIT FROM PROVIDING FOOD TO PREDATORS EVEN WHEN IT IS ALSO EDIBLE TO HERBIVORES
inferredcites →https://doi.org/10.2307/1939533openalex-snapshot
Population Regulation in Theory and Practice
inferredcites →https://doi.org/10.2307/1941332openalex-snapshot
The Predator‐Prey Interaction of the Mite Balaustium Sp. and the Pierid Butterfly Colias alexandra
inferredcites →https://doi.org/10.2307/2265694openalex-snapshot
Managing Tropical Rice Pests Through Conservation of Generalist Natural Enemies and Alternative Prey
inferredcites →https://doi.org/10.2307/2669422openalex-snapshot
Applied Survival Analysis: Regression Modeling of Time to Event Data
inferredcites →https://doi.org/10.2307/4425openalex-snapshot
Generalist and Specialist Natural Enemies in Insect Predator-Prey Interactions
inferredcites →https://doi.org/10.2307/4660openalex-snapshot
Effects of the General Predator, Notonecta (Hemiptera) Upon a Freshwater Community
inferredcites →https://doi.org/10.4039/ent1091535-12openalex-snapshot
A TECHNIQUE FOR REARING THE PREDACEOUS MITEBALAUSTIUM PUTMANI(ACARINA: ERYTHRAEIDAE), WITH NOTES ON ITS BIOLOGY AND LIFE HISTORY
inferredcites →https://doi.org/10.4039/ent123567-3openalex-snapshot
TWO NEW SPECIES OF ERYTHRAEIDAE (ACARI: PROSTIGMATA) ASSOCIATED WITH THE SPRUCE BUDWORM, CHORISTONEURA FUMIFERANA (CLEMENS) (LEPIDOPTERA: TORTRICIDAE), IN MAINE
inferredcites →https://doi.org/10.5772/30835openalex-snapshot
Generalist Predators, Food Web Complexities and Biological Pest Control in Greenhouse Crops
inferredcites →https://doi.org/10.5860/choice.30-4983openalex-snapshot
The evolution of life histories: theory and analysis
inferredcites →https://doi.org/10.5860/choice.31-0290openalex-snapshot
Applied demography for biologists with special emphasis on insects
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.5087.1.2zenodo-depositor-declared
Checklist of the oribatid mites (Acari: Oribatida) of the Republic of Colombia
inferred← citeshttps://doi.org/10.22073/pja.v7i3.37039zenodo-depositor-declared
Trophic breadth niche, prey preference and developmental time of a Balaustium \nsp. (Acari: Erythraeidae) from Argentina
inferred← citeshttps://doi.org/10.24349/biv1-2henzenodo-depositor-declared
Suitability of pollen as an alternative food source for different developmental stages of Amblyseius herbicolus (Chant) (Acari: Phytoseiidae) to facilitate predation on whitefly eggs
inferred← citeshttps://doi.org/10.1002/ps.4000openalex-snapshot
Supplemental food for Amblyseius swirskii in the control of thrips: feeding friend or foe?
inferred← citeshttps://doi.org/10.1002/ps.5312openalex-snapshot
Supplementary food for Neoseiulus californicus boosts biological control of Tetranychus urticae on strawberry
inferred← citeshttps://doi.org/10.1007/978-3-030-22304-5_16openalex-snapshot
Implementation of Integrated Pest and Disease Management in Greenhouses: From Research to the Consumer
inferred← citeshttps://doi.org/10.1007/978-3-319-15042-0_8openalex-snapshot
The Erythraeoidea (Trombidiformes: Prostigmata) as Biological Control Agents, with Special Reference to the Genus Balaustium
inferred← citeshttps://doi.org/10.1007/s10340-016-0751-xopenalex-snapshot
New opportunities for the integration of microorganisms into biological pest control systems in greenhouse crops
inferred← citeshttps://doi.org/10.1007/s10340-022-01544-xopenalex-snapshot
Potential of two omnivorous iolinid mites as predators of the tomato russet mite, Aculops lycopersici
inferred← citeshttps://doi.org/10.1007/s10340-025-01962-7openalex-snapshot
Depending on fluctuations in pest densities, a mixed diet can enhance thrips control by the generalist predator Amblyseius swirskii
inferred← citeshttps://doi.org/10.1007/s10493-022-00701-2openalex-snapshot
Estimating intrinsic growth rates of arthropods from partial life tables using predatory mites as examples
inferred← citeshttps://doi.org/10.1007/s10493-022-00723-wopenalex-snapshot
Review: predatory soil mites as biocontrol agents of above- and below-ground plant pests
inferred← citeshttps://doi.org/10.1007/s10526-014-9579-6openalex-snapshot
Approaches to conserving natural enemy populations in greenhouse crops: current methods and future prospects
inferred← citeshttps://doi.org/10.1007/s10526-016-9739-yopenalex-snapshot
Biological control of mealybugs with lacewing larvae is affected by the presence and type of supplemental prey
inferred← citeshttps://doi.org/10.1007/s10526-017-9788-xopenalex-snapshot
Patch residence time and patch preference of the predatory mite Amblyseius swirskii in relation to prey diversity
inferred← citeshttps://doi.org/10.1007/s10526-019-09993-7openalex-snapshot
Can supplementary food (pollen) modulate the functional response of a generalist predatory mite (Neoseiulus cucumeris) to its prey (Tetranychus urticae)?
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2024.105605openalex-snapshot
Does alternative food for predatory arthropods improve biological pest control? A meta-analysis
inferred← citeshttps://doi.org/10.1038/s41598-023-35363-6openalex-snapshot
Synergism of a mixed diet of Myzus persicae and egg of Ephestia kuehniella on fitness of the predator Nabis stenoferus
inferred← citeshttps://doi.org/10.1080/09583157.2020.1722798openalex-snapshot
The potential of highly nutritious frozen stages of Tyrophagus putrescentiae as a supplemental food source for the predatory mite Amblyseius swirskii
inferred← citeshttps://doi.org/10.1093/aesa/saad006openalex-snapshot
How mixture of plant and prey diets affects long-term rearing of predatory mite Neoseiulus cucumeris (Acari: Phytoseiidae)
inferred← citeshttps://doi.org/10.1111/aab.12529openalex-snapshot
The complementarity between ecological infrastructure types benefits natural enemies and pollinators in a Mediterranean vineyard agroecosystem
inferred← citeshttps://doi.org/10.1111/ecog.01401openalex-snapshot
Factors shaping latitudinal patterns in communities of arboreal spiders in northern Europe
inferred← citeshttps://doi.org/10.1111/een.13085openalex-snapshot
Benefit of actively mixing prey in a plant‐inhabiting predatory mite
inferred← citeshttps://doi.org/10.11144/javeriana.10554.38398openalex-snapshot
Soil mesostigmatid mites (Acari : Mesostigmata) inhabiting rose fields and neighboring vegetation in the Bogota plateau and their potential role as biological control agents of Frankliniella occidentalis (Insecta : Thysanoptera)
inferred← citeshttps://doi.org/10.1134/s0013873824040031openalex-snapshot
Intraguild Predation of the Acariphages Phytoseiulus persimilis Ath.-H. (Parasitiformes, Phytoseiidae) and Feltiella luboviae Fedotova et Kozlova (Diptera, Cecidomyiidae) in Shared Habitats
inferred← citeshttps://doi.org/10.11606/t.11.2019.tde-21012019-131420openalex-snapshot
Soil mesostigmatid mites (Acari: Mesostigmata) inhabiting rose fields and neighboring vegetation in the Bogota plateau and their potential role as biological control agents of Frankliniella occidentalis (Insecta: Thysanoptera)
inferred← citeshttps://doi.org/10.1653/024.097.0352openalex-snapshot
A Re-Description ofBalaustium leanderiComb. Nov. (Actinotrichida, Erythraeidae) with First First Report on Characteristics of All Active Instars and Taxonomic Notes on the Genus
inferred← citeshttps://doi.org/10.3389/fphys.2022.1015636openalex-snapshot
Innovative feedstocks for optimal mass production of the edible long-horned grasshopper, Ruspolia differens
inferred← citeshttps://doi.org/10.3390/insects14070649openalex-snapshot
Overview of Updated Control Tactics for Western Flower Thrips
inferred← citeshttps://doi.org/10.3390/plants13141953openalex-snapshot
The Potential of Two Phytoseiid Mites as Predators of the Grape Erineum Mite, Colomerus vitis
inferred← citeshttps://doi.org/10.7717/peerj.7881openalex-snapshot
Prey selectivity and the effect of diet on growth and development of a dragonfly, Sympetrum sanguineum
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