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Seasonal fluctuations of population density of the cabbage aphid,Brevicoryne brassicae (L.), in the Netherlands, and the role of its parasite,Aphidius (Diaeretiella) rapae (Curtis)

https://doi.org/10.1007/bf02089167

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What this work says

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

inferredcites →https://doi.org/10.1007/bf01982388openalex-snapshot

Een oecologisch onderzoek over de appelbloedluis,Eriosoma lanigerum (Hausm.), en haar parasietAphelinus mali (Hald.) in Nederland

inferredcites →https://doi.org/10.1007/bf01988483openalex-snapshot

Enkele gegevens over de melige koolluis (Brevicoryne Brassicae L.) in het Geestmerambacht, en zijn bestrijding

inferredcites →https://doi.org/10.1016/0022-1910(59)90024-1openalex-snapshot

The role of photoperiod and temperature in the determination of parthenogenetic and sexual forms in the aphid Megoura viciae Buckton—I

inferredcites →https://doi.org/10.1017/s0007485300002790openalex-snapshot

Preliminary Investigations on the Biology and Ecology of the Parasites and Predators ofBrevicoryne brassicae(L.)

inferredcites →https://doi.org/10.1017/s0007485300030960openalex-snapshot

Population Studies of the Pea Aphid in East Anglia

inferredcites →https://doi.org/10.1017/s0031182000016115openalex-snapshot

On the bionomics of Aphidius matricariae Hal., a braconid parasite of Myzus persicae Sulz

inferredcites →https://doi.org/10.1038/153448a0openalex-snapshot

Biological Control as a Supplement to Chemical Control of Insect Pests

inferredcites →https://doi.org/10.1038/181205b0openalex-snapshot

Influence of Parasitization on Form Determination in Aphids

inferredcites →https://doi.org/10.1086/281687openalex-snapshot

Effects of Temperature and Host Density on the Rate of Increase of an Insect Parasite

inferredcites →https://doi.org/10.1093/aesa/16.1.1openalex-snapshot

Some Braconids Parasitic on Aphids and their Life-History. (Hym.)*

inferredcites →https://doi.org/10.1093/aesa/19.2.119openalex-snapshot

Biology of the Parasites and Hyperparasites of Aphids*

inferredcites →https://doi.org/10.1093/aesa/53.2.144openalex-snapshot

The Biology, Behavior, and Morphology of Praon Palitans Muesebeck, an Internal Parasite of the Spotted Alfalfa Aphid, Therioaphis Maculata (Buckton) (Hymenoptera: Braconidae, Aphidiinae)1

inferredcites →https://doi.org/10.1093/jee/28.6.898openalex-snapshot

Effect of Host Density on Parasitism

inferredcites →https://doi.org/10.1093/jee/34.3.477openalex-snapshot

An Unusual Infestation of Cabbage Aphids, Aphis brassicae L.

inferredcites →https://doi.org/10.1093/jee/34.6.741openalex-snapshot

The Effect of Host Density on the Rate of Reproduction of Entomophagous Parasites1

inferredcites →https://doi.org/10.1093/jee/52.1.142openalex-snapshot

The Role of Imported Parasites in the Biological Control of the Spotted Alfalfa Aphid in Southern California in 19571

inferredcites →https://doi.org/10.1093/jee/52.1.154openalex-snapshot

A Synopsis of the Biologies of Three Imported Parasites of the Spotted Alfalfa Aphid12

inferredcites →https://doi.org/10.1111/j.1096-3642.1935.tb01680.xopenalex-snapshot

The Balance of Animal Populations.—Part I.

inferredcites →https://doi.org/10.1111/j.1365-3059.1952.tb00021.xopenalex-snapshot

SURVEY OF CABBAGE APHID POPULATIONS ON BRUSSELS SPROUTS, 1946–51

inferredcites →https://doi.org/10.1111/j.1365-3059.1954.tb00699.xopenalex-snapshot

SAMPLING CABBAGE APHID POPULATIONS ON BRUSSELS SPROUTS

inferredcites →https://doi.org/10.1111/j.1365-3059.1957.tb00756.xopenalex-snapshot

CABBAGE APHID ASSESSMENT AND DAMAGE IN ENGLAND AND WALES, 1946–55

inferredcites →https://doi.org/10.1111/j.1469-185x.1953.tb01382.xopenalex-snapshot

APHIDS AND VIRUS DISEASESIN POTATO CROPS

inferredcites →https://doi.org/10.1111/j.1570-7458.1959.tb02100.xopenalex-snapshot

EFFECT OF PARASITIZATION BY APHIDIUS PLATENSIS BRÈTHES ON THE DEVELOPMENTAL PHYSIOLOGY OF ITS HOST, APHIS CRACCIVORA KOCH

inferredcites →https://doi.org/10.1111/j.1744-7348.1936.tb05571.xopenalex-snapshot

OBSERVATIONS ON THE LIFE HISTORY AND CONTROL OF THE CABBAGE APHIS, BRE VICORYNE BBASSICAE L.

inferredcites →https://doi.org/10.1111/j.1744-7348.1938.tb04369.xopenalex-snapshot

PHYSIOLOGICAL RELATIONSHIPS BETWEEN INSECTS AND THEIR HOST PLANTS

inferredcites →https://doi.org/10.1111/j.1744-7348.1948.tb07397.xopenalex-snapshot

Methods of Recording Aphid Populations for Use in Research on Potato Virus Diseases

inferredcites →https://doi.org/10.1111/j.1744-7348.1948.tb07398.xopenalex-snapshot

On Estimating the Population of Aphids in A Potato Field

inferredcites →https://doi.org/10.1111/j.1744-7348.1949.tb06399.xopenalex-snapshot

FACTORS AFFECTING THE ACTIVITY OF ALATAE OF THE APHIDS MYZUS PERSICAE (SULZER) AND BREVICORYNE BRASSICAE (L.)

inferredcites →https://doi.org/10.1111/j.1744-7348.1950.tb00989.xopenalex-snapshot

THE DISTRIBUTION OF APHID INFESTATION IN RELATION TO LEAF AGE

inferredcites →https://doi.org/10.1111/j.1744-7348.1951.tb07788.xopenalex-snapshot

HOST ALTERNATION IN APHIS FABAE SCOP. I. FEEDING PREFERENCES AND FECUNDITY IN RELATION TO THE AGE AND KIND OF LEAVES

inferredcites →https://doi.org/10.1111/j.1744-7348.1951.tb07829.xopenalex-snapshot

THE INFLUENCE OF HEAT ON SOME APHIDS

inferredcites →https://doi.org/10.1146/annurev.en.04.010159.001035openalex-snapshot

Biology of Aphids

inferredcites →https://doi.org/10.1163/036551660x00035openalex-snapshot

On the Theories of Host-Parasite Interactions1

inferredcites →https://doi.org/10.1163/036551660x00053openalex-snapshot

The Natural Control of Insects in Pinewoods

inferredcites →https://doi.org/10.21248/contrib.entomol.11.7-8.792-803openalex-snapshot

Die Gattungen der Familie Aphidiidae und ihre verwandtschaftliche Zuordnung (Hymenoptera: Ichneumonoidea).

inferredcites →https://doi.org/10.2307/1493openalex-snapshot

The Natural Control of Population Balance in the Knapweed Gall-Fly (Urophora jaceana)

inferredcites →https://doi.org/10.2307/1578openalex-snapshot

The Natural Control of Animal Populations

inferredcites →https://doi.org/10.2307/954openalex-snapshot

Supplement: the Balance of Animal Populations

inferredcites →https://doi.org/10.3406/bsef.1919.26461openalex-snapshot

Description d'un Cynipide aphidiphage nouveau (Alloxysta Kiefferi, n. sp.), parasite du Puceron de la Betterave

inferredcites →https://doi.org/10.3733/hilg.v18n11p407openalex-snapshot

The most important species of aphids attacking cruciferous crops in California

inferredcites →https://doi.org/10.4039/ent8125-2openalex-snapshot

Distribution of Progeny by Chelonus texanus Cress. (Hymenoptera: Braconidae)

inferredcites →https://doi.org/10.4039/ent90179-3openalex-snapshot

Effect of Host Distribution on the Reproduction of Encarsia formosa Gahan (Hymenoptera: Chalcidoidea)

What points at this work

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

inferred← citeshttps://doi.org/10.5852/ejt.2013.53zenodo-depositor-declared

Revision of the types of species of Alloxysta described by Cameron and Fergusson (Hymenoptera: Figitidae: Charipinae) and deposited in the Natural History Museum (London), including a key to the fauna of Great Britain

inferred← citeshttps://doi.org/10.1002/ps.7002openalex-snapshot

Is what you see what you get? The relationship between field observed and laboratory observed aphid parasitism rates in canola fields

inferred← citeshttps://doi.org/10.1006/bcon.1999.0754openalex-snapshot

Generation Time Ratios—Determinants of Prey Abundance in Insect Predator–Prey Interactions

inferred← citeshttps://doi.org/10.1006/jtbi.2002.3080openalex-snapshot

Are Classical Predator–Prey Models Relevant to the Real World?

inferred← citeshttps://doi.org/10.1007/978-1-4899-6938-5_7openalex-snapshot

How the behaviour of parasites and predators promotes population stability

inferred← citeshttps://doi.org/10.1007/978-94-009-1225-0_9openalex-snapshot

Observational and Experimental Methods for the Estimation of Natality, Mortality and Dispersal

inferred← citeshttps://doi.org/10.1007/978-981-15-6149-8_6openalex-snapshot

Sucking Pests of Rapeseed-Mustard

inferred← citeshttps://doi.org/10.1007/bf00317107openalex-snapshot

Regulation of aphid populations by aphidiid wasps: does parasitoid foraging behaviour or hyperparasitism limit impact?

inferred← citeshttps://doi.org/10.1007/bf01049398openalex-snapshot

The role of experience in plant foraging by the aphid parasitoidDiaeretiella rapae (Hymenoptera: Aphidiidae)

inferred← citeshttps://doi.org/10.1007/bf02370609openalex-snapshot

Mechanische und physiologische Abwehrreaktionen einiger Blattlausarten [Aphididae] gegen Schlupfwespen [Hymenoptera]

inferred← citeshttps://doi.org/10.1007/bf02371780openalex-snapshot

Insect parasites of the green peach aphid,Myzus persicae Sulz., and their control potential

inferred← citeshttps://doi.org/10.1007/bf02372012openalex-snapshot

Évaluation en laboratoire de la toxicité pourDiaeretiella rapae [Hym.: Aphidiidae] des pesticides utilisés en traitement des parties aériennes des plantes

inferred← citeshttps://doi.org/10.1007/bf02373149openalex-snapshot

Parasitism byEphedrus cerasicola [Hym.: Aphidiidae] developing in different stages ofMyzus persicae [Hom.: Aphididae]

inferred← citeshttps://doi.org/10.1007/bf02373446openalex-snapshot

Duration of development and longevity inAphidius ervi andAphidius platensis [Hym.: Aphidiidae], two parasites ofMyzus persicae [Hom.: Aphididae]

inferred← citeshttps://doi.org/10.1007/bf02375084openalex-snapshot

Synomone-mediated interactions between the parasitoidDiaeretiella rapae andBrevicoryne brassicae under field conditions

inferred← citeshttps://doi.org/10.1007/bf02375094openalex-snapshot

Fecundity, reproductive rate, longevity, and intrinsic rate of increase of an aphidiid parasitoidLysiphlebia mirzai

inferred← citeshttps://doi.org/10.1007/bf02375098openalex-snapshot

Zur biologie des hyperparasitoidenAlloxysta fuscicornis (=AA. Ancylocera) [Hym.: Charipidae]

inferred← citeshttps://doi.org/10.1007/bf02510944openalex-snapshot

Population studies of Brevicoryne brassicae (L.), its parasites and hyperparasites in England

inferred← citeshttps://doi.org/10.1007/bf02512623openalex-snapshot

A comparative study of the searching efficiencies of a parasite and a hyperparasite

inferred← citeshttps://doi.org/10.1007/bf02981109openalex-snapshot

Is the parasitization rate ofDiaeretiella rapae influenced whenBrevicoryne brassicae feeds onbrassica plants?

inferred← citeshttps://doi.org/10.1007/bf03356527openalex-snapshot

Effects of Climate Change on Pest-Parasitoid Dynamics: Development of a Simulation Model and First Results

inferred← citeshttps://doi.org/10.1007/s004420050610openalex-snapshot

A simple Markov model for the assessment of host patch quality by foraging parasitoids

inferred← citeshttps://doi.org/10.1007/s10340-015-0721-8openalex-snapshot

Plant growth-promoting Bacillus suppress Brevicoryne brassicae field infestation and trigger density-dependent and density-independent natural enemy responses

inferred← citeshttps://doi.org/10.1007/s10526-015-9702-3openalex-snapshot

The delay in arrival of the parasitoid Diaeretiella rapae influences the efficiency of cabbage aphid biological control

inferred← citeshttps://doi.org/10.1007/s10886-020-01239-6openalex-snapshot

Multiple Attack to Inflorescences of an Annual Plant Does Not Interfere with the Attraction of Parasitoids and Pollinators

inferred← citeshttps://doi.org/10.1007/s11540-022-09540-5openalex-snapshot

Species Composition and Distribution of the Vector Aphids of PVY and PLRV in India

inferred← citeshttps://doi.org/10.1007/s41348-016-0038-8openalex-snapshot

Efficacy of crop cover netting against cabbage pests and their natural enemies and relevance of oilseed rape

inferred← citeshttps://doi.org/10.1007/s42690-021-00544-1openalex-snapshot

Incidence of the cabbage aphid, Brevicoryne brassicae L. in potato crops in India and its efficiency for transmission of potato virus Yo

inferred← citeshttps://doi.org/10.1016/0040-5809(76)90040-xopenalex-snapshot

Optimal foraging, the marginal value theorem

inferred← citeshttps://doi.org/10.1016/0261-2194(87)90071-8openalex-snapshot

Cabbage aphid control on commercial farms in the Thames Valley, UK

inferred← citeshttps://doi.org/10.1016/j.biocontrol.2004.03.010openalex-snapshot

Effects of the agricultural adjuvant Sylgard 309 and the insecticide pymetrozine on demographic parameters of the aphid parasitoid, Diaeretiella rapae

inferred← citeshttps://doi.org/10.1017/s0007485300018563openalex-snapshot

Direct measurement of host and parasitoid recruitment for assessment of total losses due to parasitism in a continuously breeding species, the cabbage aphid,Brevicoryne brassicae(L.) (Hemiptera: Aphididae)

inferred← citeshttps://doi.org/10.1017/s1742758415000260openalex-snapshot

Host stage preference and performance of the aphid parasitoid Diaeretiella rapae (Hymenoptera: Braconidae) on Brevicoryne brassicae and Lipaphis pseudobrassicae (Hemiptera: Aphididae)

inferred← citeshttps://doi.org/10.1046/j.1570-7458.1997.00126.xopenalex-snapshot

Reproduction of Diaeretiella rapae on Russian wheat aphid hosts at different temperatures

inferred← citeshttps://doi.org/10.1078/1439-1791-00071openalex-snapshot

When and why top-down regulation failsin arthropod predator-prey systems

inferred← citeshttps://doi.org/10.1079/ber2001134openalex-snapshot

Tritrophic interactions between cabbage cultivars with different resistance and fertilizer levels, cruciferous aphids and parasitoids under field conditions

inferred← citeshttps://doi.org/10.1079/cabicompendium.18686openalex-snapshot

Diaeretiella rapae

inferred← citeshttps://doi.org/10.1080/00288233.1969.10421225openalex-snapshot

A technique for studying the population dynamics of the cabbage aphid Brevicoryne brassicae (L.)

inferred← citeshttps://doi.org/10.1080/00382167.1984.9628936openalex-snapshot

Biology and Population Dynamics of the Pine Needle Aphid, Eulachnus rileyi (Williams) in Zimbabwe

inferred← citeshttps://doi.org/10.1080/01448765.1989.9754512openalex-snapshot

Bionomics of an Aphidiid ParasitoidTrioxys indicus.30. Effect of Host Plants on Reproductive and Developmental Factors

inferred← citeshttps://doi.org/10.1080/01448765.1992.9754606openalex-snapshot

Biology, Ecology and Control Efficiency of the Aphid ParasitoidTrioxys indicas:a Review and Bibliography

inferred← citeshttps://doi.org/10.1080/01448765.1994.9754680openalex-snapshot

Functional Response ofCampoletis chloridaeUchida (Hymenoptera: Ichneumonidae), a Parasitoid ofHeliothis armigera(Hübner) (Lepidoptera: Noctuidae) in an Enclosed Experimental System

inferred← citeshttps://doi.org/10.1080/01448765.1995.9754720openalex-snapshot

Sex Ratio Adjustment by a Koinobiotic Parasitoid Lysiphlebus delhiensis (Subba Rao & Sharma) (Hymenoptera: Aphidiidae) in Response to Host Size

inferred← citeshttps://doi.org/10.1080/03014223.1981.10427979openalex-snapshot

The biology of Dendrocerus carpenteri (Hymenoptera: Ceraphronidae), a parasite of Aphidius species, and field observations of Dendrocerus species as hyperparasites of Acyrthosiphon species

inferred← citeshttps://doi.org/10.1086/283062openalex-snapshot

Ecological Implications of Resource Depression

inferred← citeshttps://doi.org/10.1086/285464openalex-snapshot

Optimal Egg Distribution Among Host Patches for Parasitoids Subject to Attack by Hyperparasitoids

inferred← citeshttps://doi.org/10.1093/ee/28.1.61openalex-snapshot

Host Range and Habitats of the Aphid ParasitoidDiaeretiella rapae(Hymenoptera: Aphidiidae) in Washington State

inferred← citeshttps://doi.org/10.1093/ee/nvx108openalex-snapshot

Influence of Host Quality and Temperature on the Biology of Diaeretiella rapae (Hymenoptera: Braconidae, Aphidiinae)

inferred← citeshttps://doi.org/10.1111/j.1365-2311.1976.tb01219.xopenalex-snapshot

The searching behaviour of Anthocoris confusus (Reuter) in relation to prey density and plant surface topography

inferred← citeshttps://doi.org/10.1111/j.1365-2311.1990.tb00802.xopenalex-snapshot

Host specificity and seasonal distribution of Alloxysta pleuralis , a cynipoid hyperparasitoid of aphids in India

inferred← citeshttps://doi.org/10.1111/j.1365-2311.2006.00769.xopenalex-snapshot

Host‐related fitness trade‐offs in a presumed generalist parasitoid, Diaeretiella rapae (Hymenoptera: Aphidiidae)

inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02196.xopenalex-snapshot

Phylogeography of a parasitoid wasp (Diaeretiella rapae): no evidence of host‐associated lineages

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1971.tb03143.xopenalex-snapshot

Über Ausbreitung und Orientierung vonDiaeretiella rapae(Hymenoptera, Aphidiidae) unter Berücksichtigung der Hyperparasiten vonBrevicoryne brassicae(Homoptera, Aphididae)1,2

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1974.tb01899.xopenalex-snapshot

Auswirkung von der räuberischen GallmückeAphidoletes aphidimyza(Rond.) (Itonididae: Diptera) auf Blattlauspopulationen unter Glas

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1978.tb04054.xopenalex-snapshot

Pattern and influencing factors of emergence in Diaeretiella rapae and its parasites

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1980.tb03455.xopenalex-snapshot

Studies on the bionomics of Trioxys (Binodoxys) indicus Subba Rao and Sharma (Hym., Aphidiidae), a parasitoid of Aphis craccivora Koch (Hem., Aphididae) ‐ the area of discovery of the parasitoid

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1980.tb03512.xopenalex-snapshot

Bionomics of Trioxys (Binodoxys) indicus Subba Rao and Sharma, an aphidiid parasitoid of Aphis craccivora Koch

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1980.tb03524.xopenalex-snapshot

Bionomics of Trioxys (Binodoxys) indicus Subba Roa and Sharma, an aphidiid parasitoid of Aphis craccivora Koch

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1982.tb03571.xopenalex-snapshot

Bionomics of Trioxys (Binodoxys) indicus Subba Rao & Sharma, an aphidiid parasitoid of Aphis craccivora Koch

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1982.tb03583.xopenalex-snapshot

Bionomics of Trioxys (Binodoxys) indicus, an aphidiid parasitoid of Aphis craccivora

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1983.tb03673.xopenalex-snapshot

Bionomics of Trioxys (Binodoxys) indicus, an aphidiid parasitoid of Aphis craccivora

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1984.tb02692.xopenalex-snapshot

Bionomics of Trioxys (Binodoxys) indicus, an aphidiid parasitoid of Aphis craccivora

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1984.tb02718.xopenalex-snapshot

Functional response of Diaeretiella rapae (M'Intosh) (Hym., Aphidiidae), a parasitoid of the mustard aphid Lipaphis erysimi Kalt. (Hom., Aphididae)

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1985.tb02750.xopenalex-snapshot

Distribution, survival and hatching of overwintering eggs in the large pine aphid, Cinara pinea (Mordv.) (Hom., Lachnidae)

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1987.tb00989.xopenalex-snapshot

Impact of male on the functional response of Diaeretieila rapae (M'Intosh) (Hym., Aphidiidae), a parasitoid of Lipaphis erysimi Kalt. (Hom., Aphididae)

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1989.tb00268.xopenalex-snapshot

Life‐table studies of an aphid hyperparasitoid Alloxysta pleuralis (Cameron) (Hym., Alloxystidae)

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1990.tb00014.xopenalex-snapshot

Overwintering and hymenopterous parasitism in autumn of the cereal aphid Sitobion avenae (F.) in northern FR Germany

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1990.tb00092.xopenalex-snapshot

Behaviour of the parasitoid Lysiphlebia mirzai Shuja‐Uddin (Hym., Aphidiidae) at varying host densities

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1991.tb00296.xopenalex-snapshot

Sex ratio of the aphid parasitoid Lysiphlebus delhiensis (Subba Rao & Sharma) (Hym., Aphidiidae) in field population

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1994.tb00804.xopenalex-snapshot

Functional response of Diaeretiella rapae (McIntosh) (Hym., Aphidiidae) to Diuraphis noxia (Mordwilko) (Hom., Aphididae) hosts

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1995.tb01246.xopenalex-snapshot

Influence of age of parents Lysiphlebus delhiensis (Subba Rao and Sharma) (Hym., Aphidiidae) during copulation on progeny production and offspring sex ratio

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1995.tb01285.xopenalex-snapshot

Thermal requirements ofDiaeretiella rapae(M'Intosh) on Russian wheat aphid (Diuraphis noxiaMordwilko, Hom., Aphididae) hosts

inferred← citeshttps://doi.org/10.1111/j.1439-0418.1995.tb01307.xopenalex-snapshot

Patch time allocation and resource exploitation in aphid primary parasitoids and hyperparasitoids searching simultaneously within aphid colonies

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1963.tb00602.xopenalex-snapshot

A FIELD TECHNIQUE FOR COMPARING THE INTENSITY OF MORTALITY FACTORS ACTING ON THE CABBAGE APHID, BREVICORYNE BRASSICAE (L.) (HEM: APHIDIDAE), IN DIFFERENT AREAS OF A CROP

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1980.tb02951.xopenalex-snapshot

Egg survival in the bird cherry‐oat aphid, Rhopalosiphum padi

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1982.tb03210.xopenalex-snapshot

BIONOMICS OF TRIOXYS INDICUS, AN APHIDIID PARASITOID OF APHIS CRACCIVORA. X. SUPERPARASITISM CAUSED BY CONFINEMENT WITH THE HOST

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1983.tb03259.xopenalex-snapshot

The effect of temperature and humidity on the duration of development and hatching success of eggs of the aphid, Sitobion avenae

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1984.tb03389.xopenalex-snapshot

Oviposition preferences of a hymenopterous parasite for certain instars of its aphid host

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1986.tb00495.xopenalex-snapshot

Distribution of superparasitization in the aphid parasite, Aphidius sonchi

inferred← citeshttps://doi.org/10.1111/j.1570-7458.1996.tb00781.xopenalex-snapshot

Behavioral and physiological responses of Diaeretiella rapae to semiochemicals

inferred← citeshttps://doi.org/10.1111/j.1744-7348.1969.tb02842.xopenalex-snapshot

Experiments on integration of chemical and biological control of aphids on brussels sprouts

inferred← citeshttps://doi.org/10.1111/nph.14904openalex-snapshot

Caterpillars induce jasmonates in flowers and alter plant responses to a second attacker

inferred← citeshttps://doi.org/10.1127/entom.gen/7/1982/295openalex-snapshot

Factors Responsible for the Superparasitic Ability of the Parasitoid Wasp Trioxys indicus (Hymenoptera: Aphidiidae)

inferred← citeshttps://doi.org/10.1146/annurev.en.10.010165.001313openalex-snapshot

Insect Pests of Crucifers and Their Control

inferred← citeshttps://doi.org/10.1146/annurev.es.08.110177.001553openalex-snapshot

Aphid Ecology: Life Cycles, Polymorphism, and Population Regulation

inferred← citeshttps://doi.org/10.1303/jjaez.19.260openalex-snapshot

Differential Preference for Myzus persicae (SULZER) of Two Parasites, Diaeretiella rapae (M'INTOSH) and Aphidius gifuensis ASHMEAD

inferred← citeshttps://doi.org/10.13140/rg.2.1.2835.7282openalex-snapshot

Comparison of life table parameters of Russian wheat aphid, Diuraphis noxia, and its parasitoid, Diaeretiella rapae under constant temperatures

inferred← citeshttps://doi.org/10.1590/s0006-87052002000200007openalex-snapshot

Flutuação populacional de formas aladas de Brevicoryne brassicae (L.) (Hemiptera: Aphididae)

inferred← citeshttps://doi.org/10.1590/s0100-204x2003000500002openalex-snapshot

Exigências térmicas de Brevicoryne brassicae e previsão de picos populacionais

inferred← citeshttps://doi.org/10.2307/2402001openalex-snapshot

The Ecology of Aphis craccivora Koch and Subterranean Clover Stunt Virus in South-East Australia. II. A Model of Cowpea Aphid Populations in Temperate Pastures

inferred← citeshttps://doi.org/10.2307/2402197openalex-snapshot

Temperature Requirements of Some Aphids and Their Parasites

inferred← citeshttps://doi.org/10.2307/3074openalex-snapshot

A Model of an Aphid Population--A General Statement

inferred← citeshttps://doi.org/10.2307/3201openalex-snapshot

Insect Parasite Responses in the Development of Population Models

inferred← citeshttps://doi.org/10.2307/3260openalex-snapshot

A Model of an Aphid Population--Three Adventures

inferred← citeshttps://doi.org/10.2307/3615openalex-snapshot

A Model for Avoidance of Superparasitism by Solitary Insect Parasitoids

inferred← citeshttps://doi.org/10.2307/3725openalex-snapshot

The Numerical Responses of Insect Predators to Changes in Prey Density

inferred← citeshttps://doi.org/10.2307/3772openalex-snapshot

The Components of Arthropod Predation: I. The Prey Death-Rate

inferred← citeshttps://doi.org/10.2307/4966openalex-snapshot

The Foraging Strategy of Diaeretiella rapae

inferred← citeshttps://doi.org/10.3390/insects12010044openalex-snapshot

Hymenopteran Parasitoids of Aphid Pests within Australian Grain Production Landscapes

inferred← citeshttps://doi.org/10.4039/ent101768-7openalex-snapshot

POPULATION INCREASE OF THE CABBAGE APHID, BREVICORYNE BRASSICAE, ON DIFFERENT HOST PLANTS

inferred← citeshttps://doi.org/10.4039/ent1021567-12openalex-snapshot

HABITAT SELECTION BY THE APHID PARASITEDIAERETIELLA RAPAE(HYMENOPTERA: BRACONIDAE) AND HYPERPARASITECHARIPS BRASSICAE(HYMENOPTERA: CYNIPIDAE)

inferred← citeshttps://doi.org/10.4039/ent107919-9openalex-snapshot

THE EFFECT OF PARASITISM BY APHIDIUS SMITHI (HYMENOPTERA: APHIDIIDAE) ON REPRODUCTION AND POPULATION GROWTH OF THE PEA APHID (HOMOPTERA: APHIDIDAE)

inferred← citeshttps://doi.org/10.4039/ent115399-4openalex-snapshot

QUANTITATIVE ASSESSMENT OF APHIDIUS SMITHI (HYMENOPTERA: APHIDIIDAE): FECUNDITY, INTRINSIC RATE OF INCREASE, AND FUNCTIONAL RESPONSE

inferred← citeshttps://doi.org/10.4039/ent1161605-12openalex-snapshot

REPRODUCTION AND LONGEVITY OF CABBAGE APHID,BREVICORYNE BRASSICAE(HOMOPTERA: APHIDIDAE), PARASITIZED BYDIAERETIELLA RAPAE(HYMENOPTERA: APHIDIIDAE)

inferred← citeshttps://doi.org/10.4039/ent116861-6openalex-snapshot

POPULATION DYNAMICS OF THE CABBAGE APHID, BREVICORYNE BRASSICAE (HOMOPTERA: APHIDIDAE) AT VANCOUVER, BRITISH COLUMBIA: I. SAMPLING METHODS AND POPULATION TRENDS

inferred← citeshttps://doi.org/10.4039/ent116871-6openalex-snapshot

POPULATION DYNAMICS OF THE CABBAGE APHID, BREVICORYNE BRASSICAE (HOMOPTERA: APHIDIDAE) AT VANCOUVER, BRITISH COLUMBIA: II. DEVELOPMENT, FECUNDITY, AND LONGEVITY

inferred← citeshttps://doi.org/10.4137/ijis.s13029openalex-snapshot

Estimation of Fitness of Normal and Stylopized Paddy Pest, White Leafhopper Cofana spectra (Distant) (Hemiptera: Cicadellidae), in West Bengal, India through Correlation of Life History Traits

inferred← citeshttps://doi.org/10.5539/ijb.v11n4p42openalex-snapshot

Natural Entomophages of Brevicoryne Brassicae (L.) (Hemiptera: Aphididae) in Uzbekistan

inferred← citeshttps://doi.org/10.5772/intechopen.1008940openalex-snapshot

Mass Production and Field Application of Some Parasitoids in Egypt

inferred← citeshttps://doi.org/10.5897/jpbcs.9000077openalex-snapshot

Host selection behaviour of aphid parasitoids (Aphidiidae: Hymenoptera)

inferred← citeshttps://doi.org/10.70675/35929a77z0823z4e7bz892dz908d2b947857openalex-snapshot

Bottom-up effects of abiotic factors on aphid parasitoid specialization

inferred← citeshttps://doi.org/10.7275/18739298openalex-snapshot

Foraging behaviour of Rhagoletis pomonella, a parasite of hawthorn (Crataegus).

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