about
From plants to birds: higher avian predation rates in trees responding to insect herbivoryWhere do herbivore-induced plant volatiles go?Volatile organic compounds emitted from silver birch of different provenances across a latitudinal gradient in Finland.Smelling global climate change: mitigation of function for plant volatile organic compounds.Doubled volatile organic compound emissions from subarctic tundra under simulated climate warming.Activation of defence pathways in Scots pine bark after feeding by pine weevil (Hylobius abietis).Utilizing associational resistance for biocontrol: impacted by temperature, supported by indirect defence.Life-history strategies affect aphid preference for yellowing leaves.Plant volatile organic compounds (VOCs) in ozone (O3) polluted atmospheres: the ecological effects.Multiple stress factors and the emission of plant VOCs.Molecular plant volatile communication.Plant volatiles in polluted atmospheres: stress responses and signal degradation.Targeted use of LEDs in improvement of production efficiency through phytochemical enrichment.Effects of elevated carbon dioxide and ozone on volatile terpenoid emissions and multitrophic communication of transgenic insecticidal oilseed rape (Brassica napus).Constitutive and herbivore-inducible glucosinolate concentrations in oilseed rape (Brassica napus) leaves are not affected by Bt Cry1Ac insertion but change under elevated atmospheric CO2 and O3.Air pollution impedes plant-to-plant communication, but what is the signal?Ozone exposure triggers the emission of herbivore-induced plant volatiles, but does not disturb tritrophic signalling.Atmospheric transformation of plant volatiles disrupts host plant finding.Ozone affects growth and development of Pieris brassicae on the wild host plant Brassica nigra.Real-time monitoring of herbivore induced volatile emissions in the field.The influence of different nutrient levels on insect-induced plant volatiles in Bt and conventional oilseed rape plants.Host location behavior of Cotesia plutellae Kurdjumov (Hymenoptera: Braconidae) in ambient and moderately elevated ozone in field conditions.Response of Plutella xylostella and its parasitoid Cotesia plutellae to volatile compounds.Emission of Plutella xylostella-induced compounds from cabbages grown at elevated CO2 and orientation behavior of the natural enemies.Elevated atmospheric CO(2) affects the chemical quality of brassica plants and the growth rate of the specialist, Plutella xylostella, but not the generalist, Spodoptera littoralis.Plant-emitted semi-volatiles shape the infochemical environment and herbivore resistance of heterospecific neighbors.Birch (Betula spp.) leaves adsorb and re-release volatiles specific to neighbouring plants--a mechanism for associational herbivore resistance?How red is the red autumn leaf herring and did it lose its red color?Foliar methyl salicylate emissions indicate prolonged aphid infestation on silver birch and black alder.Effect of long-term forest fertilization on Scots pine xylem quality and wood borer performance.Effects of cyclamen mite (Phytonemus pallidus) and leaf beetle (Galerucella tenella) damage on volatile emission from strawberry (Fragaria x ananassa Duch.) plants and orientation of predatory mites (Neoseiulus cucumeris, N. californicus, and EuseiuNeedle removal by pine sawfly larvae increases branch-level VOC emissions and reduces below-ground emissions of Scots pine.Chemical changes induced by methyl jasmonate in oilseed rape grown in the laboratory and in the field.Stored human urine supplemented with wood ash as fertilizer in tomato (Solanum lycopersicum) cultivation and its impacts on fruit yield and quality.Pine weevil feeding on Norway spruce bark has a stronger impact on needle VOC emissions than enhanced ultraviolet-B radiation.Influence of carrot psyllid (Trioza apicalis) feeding or exogenous limonene or methyl jasmonate treatment on composition of carrot (Daucus carota) leaf essential oil and headspace volatiles.Isoprene emission from a subarctic peatland under enhanced UV-B radiation.New Light for Phytochemicals.Terpene Composition Complexity Controls Secondary Organic Aerosol Yields from Scots Pine Volatile Emissions.Genotypic variation in yellow autumn leaf colours explains aphid load in silver birch.
P50
Q28473214-6ACDC01A-2DA3-431F-861C-77DD3F759BE5Q28681615-90AC8E8D-D99B-48CA-9E07-EB2C949E2BD5Q30975534-41880AFB-DB2D-4D76-8C7E-8A962D6A6CB7Q33422704-667B9297-9383-44A2-8197-E480BA21FEAAQ33573918-1C3DD961-94F4-4B32-83D4-38675F0037F8Q35576911-F2EE2654-705B-48D1-99AF-3CE1A0BBEE2BQ35645709-544B1C4E-40C3-4823-99F3-9387B885A27AQ37433147-83B21EDA-240D-4FDA-8E73-216B6506C164Q37677608-7C62EA78-C6D1-40B1-BED3-D43236BD8673Q37689942-5BC1D969-6D68-4F03-8DCD-DC92D0EA16CAQ37991610-FC3203D3-86D9-4319-A280-12C5EFC67A57Q38205015-A168C992-5851-49EB-BF8A-09A1F807CDE2Q39385177-3894E213-B05C-453D-BC8C-57D76C9BA25AQ40018857-AB739826-BCEC-47FA-95CB-FA15688A7661Q40166438-20B17E51-D849-4225-9EFC-856D9F91D697Q40383416-5417584E-FAE2-495C-859D-D718826B5C25Q40498944-BDF5BF82-8482-4449-B1BD-47B02D8CB790Q41139799-B8BED7D2-BCA4-4D73-BBEB-92EA47727CBDQ41999551-B396E5B1-902A-4F67-ACF0-3EEBB9FF27B1Q42022810-E3C0CF2D-E169-4A81-9C87-589A7008D987Q42030703-966C4656-8AF3-4186-A6B5-9754AE2FD345Q42030713-B2009E9D-3BC5-422E-9211-36A16E3F6F5CQ42039968-C0AFB4F1-D39E-417F-84D5-B54A4EFDC437Q42043956-21E0A7CC-ED5A-48FB-BDB1-976F91E3B3E5Q42044407-093A29CF-8A35-448C-8588-952D36736667Q42758025-74470ED8-FF77-40D5-8A40-12528E61A9A7Q43125151-886F6468-4CB8-40CA-9FB2-00978445015BQ43153224-C24EB68F-3226-48FC-AD4F-C361CCD3EAD0Q43185292-650BFD36-6BFE-4EBA-B7C2-12C864740AB6Q44006162-E583D9B0-A821-4BA6-B8E8-E5E0C0385197Q44284783-F8EC86DC-FA03-4AE3-ADD7-15A3B66ABFE8Q44391873-46ED26CE-8A8F-4BEE-98C9-024A03D05ABBQ45241404-041FD2AB-8365-492D-ABAF-3A3413039B97Q45914997-78D442D7-41A9-424E-BF09-153D0738305EQ46385157-75B843A4-DD99-4A15-8A79-A35B17C2031CQ46773835-46E37203-506E-4111-BB38-8FDFC6900E04Q46987575-7857E77F-46D2-4B08-9D01-031AC349CC34Q49916180-19653A4F-850F-4795-9D57-D5FF8D2ACA34Q50321926-FAD81600-2E5A-4B15-8558-CD6EF8DA2AABQ50497805-F5CB61B7-6BDC-4017-AC30-9CB7E789D0AF
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jarmo K Holopainen
@ast
Jarmo K Holopainen
@en
Jarmo K Holopainen
@es
Jarmo K Holopainen
@nl
Jarmo K Holopainen
@sl
type
label
Jarmo K Holopainen
@ast
Jarmo K Holopainen
@en
Jarmo K Holopainen
@es
Jarmo K Holopainen
@nl
Jarmo K Holopainen
@sl
prefLabel
Jarmo K Holopainen
@ast
Jarmo K Holopainen
@en
Jarmo K Holopainen
@es
Jarmo K Holopainen
@nl
Jarmo K Holopainen
@sl
P106
P21
P31
P496
0000-0001-5026-3245
P569
2000-01-01T00:00:00Z