Region
Global
2251 AI-consensus-verified claims tagged with regional_context = "Global".
Top entities in this region
- Solanum lycopersicumGarden Tomatoplantae 123 claims
- Triticum aestivumWheatplantae 103 claims
- Zea maysCornplantae 98 claims
- Solanum tuberosumIrish Potatoplantae 92 claims
- Malus domesticaAlmindelig æbleplantae 61 claims
- Capsicum annuumChilli / Paprikaplantae 54 claims
- Oryza sativaAsian riceplantae 50 claims
- Vitis viniferaCommon Grapevineplantae 39 claims
- Aphididae (family)other 37 claims
- Glycine maxEdamameplantae 37 claims
- Hordeum vulgareBarleyplantae 37 claims
- Insecta (class)other 36 claims
attracts natural enemy
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“increasing noncrop species diversity within and around the fields (e.g., flower strips, hedgerows”
Tamburini G., Bommarco R., Wanger T.C., Kremen C., van der Heijden M.G.A., Liebman M., Hallin S. (2020) · Agricultural diversification promotes multiple ecosystem services without compromising yield · p. 1 #6496461
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“landscapes with higher proportions of semi-natural areas exhibited lower pest abundance”
Veres A., Petit S., Conord C., Lavigne C. (2013) · p. 1 #6496020
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“Two custard apple crops... were visited exclusively by non-bee taxa”
Rader R., Bartomeus I., Garibaldi L.A., Garratt M.P.D., Howlett B.G., Winfree R., Cunningham S.A., Mayfield M.M., et al. (2015) · p. 3 #6495990
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“contribution to visitation by non-bees differed markedly (5-80%)”
Rader R., Bartomeus I., Garibaldi L.A., Garratt M.P.D., Howlett B.G., Winfree R., Cunningham S.A., Mayfield M.M., et al. (2015) · p. 3 #6495989
biocontrol
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“Bacillus spp., Pseudomonas spp., Trichoderma spp., etc., and is conferred through plant hormone-mediated signalling”
· p. 1510 #6496459
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“ISR has proven to be an effective strategy in the management of a variety of bacterial pathogens, including... R. solanacearum”
· p. 1510 #6496458
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“Bacillus spp., Pseudomonas spp., Trichoderma spp., etc.”
· p. 1510 #6496457
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“use of Agrobacterium radiobacter strain K84 in the protection of exposed surfaces of woody plant cuttings from crown gall”
· p. 1509 #6496456
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“Spined soldier bug (Podisus maculiventris)”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 51 #6496434
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“anthocorid bugs benefit from alternative prey when their preferred prey, western flower thrips, are scarce”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 25 #6496433
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“Big-eyed bug with whitefly (Geocoris spp.)”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 51 #6496432
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“predatory syrphid flies, lady beetles and soft-winged flower beetles”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 25 #6496431
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“Green lacewing adult (Chrysoperla carnea)”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 52 #6496430
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“boosted populations of predatory syrphid flies, lady beetles”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 25 #6496429
- Apanteles rubecula preysOn Pieris rapae
“two parasites (Trichogramma evanescens and Apanteles rebecula)”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 25 #6496414
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“cabbage butterflies are the preferred host for two parasites (Trichogramma evanescens and Apanteles rebecula)”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 25 #6496413
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“Southern green stink bug eggs being parasitized by Trissolcus basalis”
Altieri M.A., Nicholls C.I., Fritz M.A. (2005) · p. 8 #6496407
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“Biopesticides based on Bacillus thuringiensis (Bt) should be used as the first option”
Ebert A.W., Wu T-h., Wang S-t. (2011) · p. 5 #6496281
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“The larvae feed on sucking insects such as aphids”
Luther G.C., Srinivasan R. (2010) #6496212
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“All kinds of dragonflies feed on pests”
Luther G.C., Srinivasan R. (2010) #6496211
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“Lacewings and their larvae feed on...mites”
Luther G.C., Srinivasan R. (2010) #6496210
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“Lacewings and their larvae feed on...small caterpillars”
Luther G.C., Srinivasan R. (2010) #6496209
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“Lacewings and their larvae feed on aphids, leafhoppers”
Luther G.C., Srinivasan R. (2010) #6496208
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“Lacewings and their larvae feed on aphids”
Luther G.C., Srinivasan R. (2010) #6496207
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“Earwigs prey on pests and decompose organic matter in the soil”
Luther G.C., Srinivasan R. (2010) #6496206
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“Robber flies hunt many kinds of insects”
Luther G.C., Srinivasan R. (2010) #6496205
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“many small wasps kill pests by laying eggs in the pest's body”
Luther G.C., Srinivasan R. (2010) #6496204
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“Many kinds of large wasps attack pests”
Luther G.C., Srinivasan R. (2010) #6496203
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“Ladybird beetles and their larvae feed on...spider mites”
Luther G.C., Srinivasan R. (2010) #6496202
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“Ladybird beetles and their larvae feed on...scale insects”
Luther G.C., Srinivasan R. (2010) #6496201
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“Ladybird beetles and their larvae feed on...mealybugs”
Luther G.C., Srinivasan R. (2010) #6496200
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“Ladybird beetles and their larvae feed on...whiteflies”
Luther G.C., Srinivasan R. (2010) #6496199
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“Ladybird beetles and their larvae feed on vegetable pests such as aphids”
Luther G.C., Srinivasan R. (2010) #6496198
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“jumping spiders, search for and kill pests”
Luther G.C., Srinivasan R. (2010) #6496197
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“All spiders are friends of the farmer because they kill and eat pests”
Luther G.C., Srinivasan R. (2010) #6496196
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“Praying mantids approach pests very slowly and then grab them”
Luther G.C., Srinivasan R. (2010) #6496195
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“larvae of some species feed on... aphids”
Rader R., Bartomeus I., Garibaldi L.A., Garratt M.P.D., Howlett B.G., Winfree R., Cunningham S.A., Mayfield M.M., et al. (2015) · p. 4 #6495948
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“soils in which plants do not suffer from certain diseases ... competition for nutrients ... parasitism, mycoparasitism and amensalism”
Philippot L., Raaijmakers J.M., Lemanceau P., van der Putten W.H. (2013) #6495944
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“Lepidoptera, Coleoptera and Diptera”
Oerke E.-C. (2006) · p. 33 #6495914
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“Bacillus thuringiensis ... toxic metabolite ... Lepidoptera, Coleoptera and Diptera”
Oerke E.-C. (2006) · p. 33 #6495913
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“from the Sebacinales order, i.e. Piriformospora”
Mendes R., Garbeva P., Raaijmakers J.M. (2013) · p. 6 #6495888
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“agrocin 84 produced by Agrobacterium radiobacter...exhibit antibiotic activities against closely related genera”
Mendes R., Garbeva P., Raaijmakers J.M. (2013) · p. 7 #6495887
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“rhizobacteria belonging to the Proteobacteria and Firmicutes, i.e. Pseudomonas and Bacillus”
Mendes R., Garbeva P., Raaijmakers J.M. (2013) · p. 6 #6495886
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“antibiosis...competition for trace elements...induced systemic resistance”
Mendes R., Garbeva P., Raaijmakers J.M. (2013) · p. 7 #6495885
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“fungi from the Deuteromycetes, i.e. Trichoderma and Gliocladium”
Mendes R., Garbeva P., Raaijmakers J.M. (2013) · p. 6 #6495884
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“Trichoderma species have received considerable attention for the production of antimicrobial compounds”
Mendes R., Garbeva P., Raaijmakers J.M. (2013) · p. 7 #6495883
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“ichneumonid wasps”
Kuepper G., Dodson M., Duncan J. (2016) · p. 8 #6495614
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“Parasites include a wide range of fly and wasp species including tachinid flies”
Kuepper G., Dodson M., Duncan J. (2016) · p. 8 #6495612
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“hover flies”
Kuepper G., Dodson M., Duncan J. (2016) · p. 8 #6495611
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“lacewings”
Kuepper G., Dodson M., Duncan J. (2016) · p. 8 #6495610
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“DAPG, a key factor in the antagonistic activity of P. fluorescens CHA0”
Berendsen R.L., Pieterse C.M.J., Bakker P.A.H.M. (2012) · p. 482 #6495578
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“Pseudomonas spp. that produce the antifungal 2,4-diacetylphloroglucinol”
Berendsen R.L., Pieterse C.M.J., Bakker P.A.H.M. (2012) · p. 480 #6495577
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“expression of the DAPG biosynthesis gene phlA in CHA0 was induced upon infection by Pythium”
Berendsen R.L., Pieterse C.M.J., Bakker P.A.H.M. (2012) · p. 484 #6495563
- Paenibacillus polymyxa SQR-21 pathogenOf Fusarium oxysporum f. sp. niveum
“Paenibacillus polymyxa SQR-21 systemically affects root exudates of watermelon”
Berendsen R.L., Pieterse C.M.J., Bakker P.A.H.M. (2012) · p. 483 #6495562
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“build-up of antagonistic fluorescent Pseudomonas spp. that produce 2,4-diacetylphloroglucinol”
Berendsen R.L., Pieterse C.M.J., Bakker P.A.H.M. (2012) · p. 480 #6495558
- Nematoda preysOn Insecta
“predators ... parasitoids ... or nematodes, targeted against insect and mite pests”
Bale J. S., van Lenteren J. C., Bigler F. (2007) #6495551
- Parasitoidea preysOn Insecta
“insects that parasitize other insects (parasitoids) ... targeted against insect and mite pests”
Bale J. S., van Lenteren J. C., Bigler F. (2007) #6495550
- Predatory insects and mites preysOn Arthropoda
“Many biological control schemes use predatory insects and mites”
Bale J. S., van Lenteren J. C., Bigler F. (2007) #6495549
- Pseudomonas chlororaphis preysOn seed-borne fungal pathogens
“Pseudomonas chlororaphis used for seed treatment against seed-borne diseases of barley and wheat”
Bale J. S., van Lenteren J. C., Bigler F. (2007) #6495548
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“Trichogramma pretiosum Hymenoptera North and Latin America, Aus Lepidopterans 1974 L”
van Lenteren J.C. (2012) · p. 9 #6495528
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“Neoseiulus cucumeris Acari Europe, Africa, Americas, Asia, Aus/NZ Thrips, mites 1985 L”
van Lenteren J.C. (2012) · p. 7 #6495527
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“Orius laevigatus Heteroptera Europe, Africa North, Asia Thrips 1993 L”
van Lenteren J.C. (2012) · p. 8 #6495526
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“Heterorhabditis bacteriophora Nematoda Europe, Africa North, North America, Aus Coleopterans 1984 L”
van Lenteren J.C. (2012) · p. 6 #6495525
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“Cryptolaemus montrouzieri Coleoptera Europe, Africa, Americas, Asia, Aus/NZ Coccids, pseudococcids 1917 L”
van Lenteren J.C. (2012) · p. 5 #6495524
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“Aphidius colemani Hymenoptera Europe, Africa, Americas, Asia, Aus/NZ Aphids 1991 L”
van Lenteren J.C. (2012) · p. 4 #6495522
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“Amblyseius swirskii Acari Europe, Africa, Americas, Asia Mites, thrips, whiteflies 2005 L”
van Lenteren J.C. (2012) · p. 3 #6495521
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“Trichogramma dendrolimi Hymenoptera Europe, Asia Lepidopterans 1950 L”
van Lenteren J.C. (2012) · p. 9 #6495520
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“Phytoseiulus persimilis Acari Europe, Africa, Americas, Asia, Aus/NZ Mites 1968 L”
van Lenteren J.C. (2012) · p. 8 #6495517
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“Aphidius ervi Hymenoptera Europe, Africa North, Americas, Asia Aphids 1996 L”
van Lenteren J.C. (2012) · p. 4 #6495513
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“Aphidoletes aphidimyza Diptera Europe, Africa, Americas, Asia Aphids 1989 L”
van Lenteren J.C. (2012) · p. 4 #6495512
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“Trichogramma pretiosum Hymenoptera North and Latin America, Aus Lepidopterans 1974 L”
van Lenteren J.C. (2012) · p. 9 #6495511
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“Neoseiulus cucumeris Acari Europe, Africa, Americas, Asia, Aus/NZ Thrips, mites 1985 L”
van Lenteren J.C. (2012) · p. 7 #6495510
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“Orius laevigatus Heteroptera Europe, Africa North, Asia Thrips 1993 L”
van Lenteren J.C. (2012) · p. 8 #6495509
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“Heterorhabditis bacteriophora Nematoda Europe, Africa North, North America, Aus Coleopterans 1984 L”
van Lenteren J.C. (2012) · p. 6 #6495508
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“Cryptolaemus montrouzieri Coleoptera Europe, Africa, Americas, Asia, Aus/NZ Coccids, pseudococcids 1917 L”
van Lenteren J.C. (2012) · p. 5 #6495507
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“Aphidius colemani Hymenoptera Europe, Africa, Americas, Asia, Aus/NZ Aphids 1991 L”
van Lenteren J.C. (2012) · p. 4 #6495505
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“Amblyseius swirskii Acari Europe, Africa, Americas, Asia Mites, thrips, whiteflies 2005 L”
van Lenteren J.C. (2012) · p. 3 #6495504
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“Trichogramma dendrolimi Hymenoptera Europe, Asia Lepidopterans 1950 L”
van Lenteren J.C. (2012) · p. 9 #6495503
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“Phytoseiulus persimilis Acari Europe, Africa, Americas, Asia, Aus/NZ Mites 1968 L”
van Lenteren J.C. (2012) · p. 8 #6495502
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“Encarsia formosa Hymenoptera Europe, Africa, Americas, Asia, Aus/NZ Whiteflies 1926 L”
van Lenteren J.C. (2012) · p. 6 #6495501
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“Aphidius ervi Hymenoptera Europe, Africa North, Americas, Asia Aphids 1996 L”
van Lenteren J.C. (2012) · p. 4 #6495497
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“Aphidoletes aphidimyza Diptera Europe, Africa, Americas, Asia Aphids 1989 L”
van Lenteren J.C. (2012) · p. 4 #6495496
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“Trichogramma pretiosum Hymenoptera North and Latin America, Aus Lepidopterans 1974 L”
van Lenteren J.C. (2012) · p. 9 #6495495
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“Neoseiulus cucumeris Acari Europe, Africa, Americas, Asia, Aus/NZ Thrips, mites 1985 L”
van Lenteren J.C. (2012) · p. 7 #6495494
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“Orius laevigatus Heteroptera Europe, Africa North, Asia Thrips 1993 L”
van Lenteren J.C. (2012) · p. 8 #6495493
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“Heterorhabditis bacteriophora Nematoda Europe, Africa North, North America, Aus Coleopterans 1984 L”
van Lenteren J.C. (2012) · p. 6 #6495492
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“Cryptolaemus montrouzieri Coleoptera Europe, Africa, Americas, Asia, Aus/NZ Coccids, pseudococcids 1917 L”
van Lenteren J.C. (2012) · p. 5 #6495491
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“Aphidius colemani Hymenoptera Europe, Africa, Americas, Asia, Aus/NZ Aphids 1991 L”
van Lenteren J.C. (2012) · p. 4 #6495489
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“Amblyseius swirskii Acari Europe, Africa, Americas, Asia Mites, thrips, whiteflies 2005 L”
van Lenteren J.C. (2012) · p. 3 #6495488
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“Trichogramma dendrolimi Hymenoptera Europe, Asia Lepidopterans 1950 L”
van Lenteren J.C. (2012) · p. 9 #6495487
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“Phytoseiulus persimilis Acari Europe, Africa, Americas, Asia, Aus/NZ Mites 1968 L”
van Lenteren J.C. (2012) · p. 8 #6495486
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“Encarsia formosa Hymenoptera Europe, Africa, Americas, Asia, Aus/NZ Whiteflies 1926 L”
van Lenteren J.C. (2012) · p. 6 #6495485
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“Encarsia formosa Hymenoptera Europe, Africa, Americas, Asia, Aus/NZ Whiteflies 1926 L”
van Lenteren J.C. (2012) · p. 6 #6495483
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“Phytoseiulus persimilis Acari Europe, Africa, Americas, Asia, Aus/NZ Mites 1968 L”
van Lenteren J.C. (2012) · p. 8 #6495481
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“Phytoseiulus persimilis Acari Europe, Africa, Americas, Asia, Aus/NZ Mites 1968 L”
van Lenteren J.C. (2012) · p. 8 #6495475
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“Diversification practices targeting the aboveground environment ... increased pest control”
Tamburini G., Bommarco R., Wanger T.C., Kremen C., van der Heijden M.G.A., Liebman M., Hallin S. (2020) · Agricultural diversification promotes multiple ecosystem services without compromising yield · p. 3 #6495352
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“bee declines reduce crop pollination under intensive land use”
Outhwaite C.L., McCann P., Newbold T. (2022) · Agriculture and climate change are reshaping insect biodiversity worldwide · p. 3 #6495221
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“predatory insects decline steeply under intensive land use”
Outhwaite C.L., McCann P., Newbold T. (2022) · Agriculture and climate change are reshaping insect biodiversity worldwide · p. 3 #6495220
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“diversified systems enhance natural enemy populations and biological control”
HLPE (High Level Panel of Experts on Food Security and Nutrition) (2019) · Agroecological and Other Innovative Approaches for Sustainable Agriculture and Food Systems that Enhance Food Security and Nutrition #6495213
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“parasitoids contribute to natural enemy diversity and pest suppression”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production #6495192
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“natural enemies suppress pests; stronger in diverse enemy communities”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production #6495191
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“enemy diversity linked to crop production benefits globally”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production #6495190
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“natural enemies suppress pest populations across crop systems”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production #6495189
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“predator diversity suppresses herbivore pests in agricultural landscapes”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production · p. 2 #6495188
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“natural enemy diversity including parasitoids reduces herbivore abundance”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production · p. 2 #6495187
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“natural enemy diversity significantly reduced herbivore abundance across 89 studies”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production · p. 1 #6495186
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“natural enemy community including predators reduces herbivore pressure”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production · p. 2 #6495184
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“natural enemy diversity reduced herbivore abundance across 89 studies”
Dainese M., Martin E.A., Aizen M.A., Albrecht M., Bartomeus I., Bommarco R., Carvalheiro L.G., Chaplin-Kramer R., Gagic V., Garibaldi L.A., Ghazoul J., Grab H., Jonsson M., Karp D.S., Kennedy C.M., Kleijn D., Kremen C., Landis D.A., Letourneau D.K., Marini L., Poveda K., Rader R., Smith H.G., Tscharntke T., Winfree R., Zhang W., Zou Y., et al. (2019) · A global synthesis reveals biodiversity-mediated benefits for crop production · p. 1 #6495176
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“Sciomyzidae is larval parasitoid of snails, slugs”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 321 #6495162
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“70% of their known host species”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 322 #6495156
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“Feltiella acarisuga, is a biocontrol agent for two-spotted spider mites”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 321 #6495155
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“eating plant-sucking insects, like thrips and aphids”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 318 #6495154
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“well-known endoparasitoids of whiteflies, nearly cosmopolitan”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 300 #6495140
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“can parasitise the sweet potato whitefly (Bemisia tabaci)”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 304 #6495139
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“best used for preventing the establishment of the greenhouse whitefly”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 304 #6495138
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“ectoparasitoids of diaspidid scales, the most widely used in applied biocontrol”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 295 #6495136
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“E. pergandiella prefers second and third instar nymphs”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 293 #6495135
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“selected flowers as nectar resources had an impact on parasitisation”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 273 #6495121
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“Trissolcus japonicus the primary candidate for biocontrol of Halyomorpha halys”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 274 #6495119
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“Releasing Trissolcus basalis in mass into soybean fields”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 275 #6495118
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“T. remus is also reported from the eggs of S. litura and S. exigua”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 271 #6495113
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“Phanuromyia and crassiclava Telenomus, parasitoids of planthopper eggs, the fulgorids”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 268 #6495081
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“Members of genus Telenomus primarily parasitoids of Lepidoptera”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 268 #6495079
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“The age of host eggs affects oviposition of Telenomus podisi”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 268 #6495078
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“Telenomus busseolae, the egg parasitoid of Sesamia spp., attacking cereals”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 268 #6495077
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“Diglyphus spp. against Liriomyza spp.”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 214 #6495064
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“Trichogramma achaeae in biological control of Tuta absoluta in greenhouses”
Das B.C., et al. (2021) · Parasitoids in Pest Management · p. 183 #6495048
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“Neohydronomus affinis Hustache... Water lettuce weevil”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495024
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“Cassida rubiginosa Muller... Thistle tortoise beetle”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495022
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“Botanophila seneciella (Meade)... Ragwort seed fly”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495020
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“Bruchidius villosus (Fabricius)... Broom seed beetle”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495019
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“management of water hyacinth by Neochetina eichhorniae and Orthogalumna terebrantis”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 298 #6495016
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“Bactra verutana... Javelin moth”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495014
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“Agasicles hygrophila... Alligator weed Flea beetle”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495013
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“Octotoma scabripennis... Lantana leaf beetle”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 299 #6495012
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“high potential for controlling container breeding vectors, such as Aedes albopictus and Ae. Aegypti”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 291 #6495010
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“larvae of F. acarisuga consume an average of 175.4 T. cinnabarinus eggs”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 272 #6495003
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“It attacks spider mite, including Oligonychus sp., P. citri, T. urticae, and T. cinnabarinus”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 272 #6495002
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“F. acarisuga is a spider mite predator with a nearly cosmopolitan distribution”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 272 #6495001
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“feeds on eggs, larvae, nymphs, and adults of T. urticae, and it can be used as a biocontrol agent”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 270 #6494992
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“T. pyri has been reported as the most important predator of P. ulmi, Calepitrimerus vitis, and T. urticae”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 264 #6494974
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“T. pyri has been reported as the most important predator of P. ulmi”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 264 #6494973
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“E. finlandicus is one of the most important predators of phytophagous mites worldwide, especially in orchards”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 263 #6494970
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“C. lactis is conventionally used as the primary food source”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 261 #6494961
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“Typhlodromus pyri (Phytoseiidae)”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 249 #6494947
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“Panonychus citri Amblyseius largoensis ... Galendromus occidentalis”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 249 #6494946
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“Stethorus punctillum, S. gilvifrons (Coccinellidae)”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 249 #6494945
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“Phytoseiulus macropilis is categorized as a specialized predator of Tetranychus species”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 260 #6494944
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“Phytoseiulus longipes... has the potential to control Tetranychus pacificus McGregor, T. evansi”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 260 #6494943
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“the most common predator encountered on coconut mite, Aceria guerreronis on coconut palms”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 256 #6494942
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“the most frequent and abundant predator associated with the red palm mite, Raoiella indica”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 256 #6494941
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“it can keep the population of T. urticae, P. ulmi, broad mites... under the economic injury levels in apple orchards”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 255 #6494940
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“Neoseiulus californicus is one of the major phytoseiid predators of spider mites”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 258 #6494939
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“When N. cucumeris is fed on A. lycopersici and T. urticae”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 256 #6494938
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“It was the first phytoseiid mite found to feed on thrips”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 256 #6494937
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“Polyphagotarsonemus latus”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 253 #6494936
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“the females consumed an average of 169.40 specimens of P. oleivora”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 253 #6494935
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“Bemisia tabaci (Gennadius)”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 253 #6494934
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“such as Frankliniella occidentalis (Pergande)”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 253 #6494933
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“Tetranychus cinnabarinus Phytoseiulus persimilis (Phytoseiidae)”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 249 #6494932
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“P. persimilis used for biocontrol of T. urticae was one of the earliest biocontrol agents”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 259 #6494931
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“E. balteatus and Sphaerophoria scripta (Linnaeus) were found to be the predators bringing down aphid population”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 237 #6494920
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“Scaeva pyrastri (Linnaeus) ate 550 B. brassicae”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 232 #6494916
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“E. corollae consumed on an average 346 Capitophorus eleagni”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 232 #6494914
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“Episyrphus balteatus ... Myzus persicae”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 232 #6494913
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“E. balteatus fed on 416 Aphis pomi (De Geer) during its development”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 232 #6494912
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“Episyrphus balteatus ... Brevicoryne brassicae”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 232 #6494911
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“the ladybird Hippodamia variegata when fed on the aphid prey”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 196 #6494897
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“Britto et al. (2009) in ladybird, Stethorus tridens”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 200 #6494896
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“C. bipustulatus reared on oleander scale, Aspidiotus nerii Bouche”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 206 #6494895
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“the ladybird exhibited type II functional response on temperature ranging from 19 degrees C to 27 degrees C”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 205 #6494894
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“Harmonia axyridis (Pallas) ... olfactory reactions ... to alarm pheromone of green peach aphid”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 204 #6494891
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“Stethorus punctum (LeConte), selected its prey according to its quality”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 202 #6494890
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“pea aphid, A. pisum, to be the most suitable prey for C. septempunctata”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 196 #6494889
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“most successful biocontrol agents of aphids and other soft-bodied insect pests”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 188 #6494888
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“capable of climbing plants to lower heights and feed on foliar pests like aphids”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 182 #6494887
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“they prey upon slugs and late instar caterpillars”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 182 #6494885
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“excellent predators of eggs and pupae of insect pests besides caterpillars, especially of borers and armyworm”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 179 #6494854
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“have specialized mouthparts to dig snails from their shells... used effectively to control slugs in greenhouses”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 179 #6494853
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“Calosoma species, along with Carabus nemoralis, is being utilized in gypsy moth control”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 179 #6494852
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“generalist predator of over 100 species of insects, including approximately 50 different crop pests”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 141 #6494838
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“most known as predators of aphids and thrips”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 117 #6494831
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“Species of Stethoconus are considered obligate lace bug predators”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 109 #6494830
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“N. tenuis and M. pygmaeus are produced in large numbers by different private companies”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 109 #6494827
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“Both the predators consume more numbers of T. absoluta eggs”
Bhagyasree S.N., Anokhe Archana, Shashank P.R., Patel C.H. (2022) · Insect Predators in Pest Management · p. 110 #6494826
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“arrest both parasitoids, lacewings and cocinellid predators”
Dent D. (2000) · Insect Pest Management, 2nd Edition #6494786
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“contact with aphid, scale and mealybug honeydew arrest both parasitoids, lacewings and cocinellid predators”
Dent D. (2000) · Insect Pest Management, 2nd Edition #6494785
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“type II functional response curve for the aphid parasitoid Aphidius sonchi”
Dent D. (2000) · Insect Pest Management, 2nd Edition #6494758
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“B. amyloliquefaciens (e.g. LUMIALZA®)”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition #6494739
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“increase in chitinase-producing microbes ... thought to degrade the chitin-rich eggshells of nematodes”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition #6494734
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“serine proteases from P. chlamydosporia, P. lilacinum”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition #6494733
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“serine proteases from P. chlamydosporia, P. lilacinum and P. suchlasporium”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition #6494729
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“Trichoderma spp., P. chlamydosporia, P. lilacinum and even non-virulent strains of Fusarium oxysporum”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 462 #6494728
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“Pochonia chlamydosporia ..., Hirsutella rhossiliensis, Dactylella oviparasitica and Trichoderma spp.”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 455 #6494727
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“rhizosphere bacteria (e.g. Pseudomonas spp., Agrobacterium radiobacter and Bacillus subtilis) may reduce nematode damage”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 460 #6494726
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“Hirsutella rhossiliensis, Dactylella oviparasitica and Trichoderma spp.”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 455 #6494725
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“endospores germinate either immediately ... or later when the nematode has entered the root and initiated a feeding site (e.g. Meloidogyne spp.)”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 458 #6494724
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“Arthrobotrys oligospora is a good saprophytic competitor”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 457 #6494723
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“Catenaria anguillulae, which attack vermiform nematodes”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 456 #6494722
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“Sporulating hyphae of Hirsutella rhossiliensis growing out of an infected juvenile of Heterodera schachtii”
Perry R.N., Moens M., Jones J.T. (2024) · Plant Nematology, 3rd Edition · p. 456 #6494721