about
Diversity of frankiae in soils from five continents.Arbuscular mycorrhizal fungal community differs between a coexisting native shrub and introduced annual grass.Immobilizing nitrogen to control plant invasion.Phytotoxic polyacetylenes from roots of Russian knapweed (Acroptilon repens (L.) DC.).Diversity of frankiae in root nodules of Morella pensylvanica grown in soils from five continents.Selenium hyperaccumulation by Astragalus (Fabaceae) does not inhibit root nodule symbiosis.White locoweed toxicity is facilitated by a fungal endophyte and nitrogen-fixing bacteria.Optimizing seed mixture diversity and seeding rates for grassland restorationTwenty-five years of sagebrush steppe plant community development following seed additionThe Use of Seedbed Modifications and Wood Chips to Accelerate Restoration of Well Pad Sites in Western Colorado, U.S.AEarly seral plant species’ interactions with an arbuscular mycorrhizal fungi community are highly variableNative cover crops suppress exotic annuals and favor native perennials in a greenhouse competition experimentA molecular approach to understanding plant–plant interactions in the context of invasion biologyThe role of the native soil community in the invasion ecology of spotted (Centaurea maculosa auct. non Lam.) and diffuse (Centaurea diffusa Lam.) knapweedNo evidence for root-mediated allelopathy in Centaurea solstitialis, a species in a commonly allelopathic genusManganese toxicity thresholds for restoration grass speciesEnhanced decomposition of selenium hyperaccumulator litter in a seleniferous habitat—evidence for specialist decomposers?Variation in Frankia Populations of the Elaeagnus Host Infection Group in Nodules of Six Host Plant Species after Inoculation with SoilManganese and Zinc Toxicity Thresholds for Mountain and Geyer WillowThe floral volatile, methyl benzoate, from snapdragon (Antirrhinum majus) triggers phytotoxic effects in Arabidopsis thaliana
P50
Q33495014-4142587C-5C3D-4B64-BF1D-B74EC1CBE29BQ34366597-8B259529-94E2-46D0-B7DA-AD488DFA1577Q37729927-EA586536-5AD0-434B-8BA1-29FB07F26425Q46370211-E14DABF8-C345-4165-838D-05A241F6D0C2Q48070993-4CF258C1-1E37-4550-98B9-ECE45BC63EABQ51544148-60F6D6D1-F8D9-4ED3-BEB5-D07ED0ECB358Q51705147-607E3723-F998-4DDC-8875-E48A89B79EB5Q56332816-41761552-3F55-4859-9D6A-1050E40A3191Q56551195-BADEF04C-E493-4B3D-A80C-81BE2CEDE32CQ56556835-BF8EC505-9EAF-47BA-90EC-D3955BDA9EF1Q56750597-4874B742-E8C6-4B57-A761-E534B9C668C9Q56770398-E219370D-ABE2-4943-BB09-128C2A84D2FCQ56776023-96C0C892-2390-4668-9178-A41991C00221Q56780936-64BEB322-DAE0-41CC-AEBE-86853B4DA442Q57043585-E68D7770-E417-43A5-BE3F-FCD1D77EE9D5Q57140020-AE9C41EA-8B86-48A9-85A0-AA421E4D3DE0Q60400101-99F61AE8-1DCD-441E-9B0E-A84B95C5F78AQ60400111-0E5B4491-3854-409D-87E1-BF174FB2AFCEQ60400118-9744872E-B0A4-4B63-8AD3-BE58F2DA8FEAQ60400119-3FEEEC91-06C6-4D77-866B-7D28EDD27979
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Mark W. Paschke
@ast
Mark W. Paschke
@en
Mark W. Paschke
@es
Mark W. Paschke
@nl
Mark W. Paschke
@sl
type
label
Mark W. Paschke
@ast
Mark W. Paschke
@en
Mark W. Paschke
@es
Mark W. Paschke
@nl
Mark W. Paschke
@sl
prefLabel
Mark W. Paschke
@ast
Mark W. Paschke
@en
Mark W. Paschke
@es
Mark W. Paschke
@nl
Mark W. Paschke
@sl
P106
P1153
7003883322
P31
P496
0000-0002-6345-5905