about
Ice cover extent drives phytoplankton and bacterial community structure in a large north-temperate lake: implications for a warming climate.Ecology under lake iceLake Superior supports novel clusters of cyanobacterial picoplanktonA mesoscale phytoplankton bloom in the polar Southern Ocean stimulated by iron fertilization.Phylogenies of microcystin-producing cyanobacteria in the lower Laurentian Great Lakes suggest extensive genetic connectivityAbundance and diversity of ammonia-oxidizing archaea and bacteria in sediments of trophic end members of the Laurentian Great Lakes, Erie and Superior.Luminescent whole-cell cyanobacterial bioreporter for measuring Fe availability in diverse marine environments.Plasticity of Total and Intracellular Phosphorus Quotas in Microcystis aeruginosa Cultures and Lake Erie Algal Assemblages.Freshwater ice as habitat: partitioning of phytoplankton and bacteria between ice and water in central European reservoirs.Global solutions to regional problems: Collecting global expertise to address the problem of harmful cyanobacterial blooms. A Lake Erie case study.Cyanobacterial bioreporters as sensors of nutrient availability.Ecophysiological Examination of the Lake Erie Microcystis Bloom in 2014: Linkages between Biology and the Water Supply Shutdown of Toledo, OH.Detection and expression of the phosphonate transporter gene phnD in marine and freshwater picocyanobacteria.Environmental Pseudomonads Inhibit Cystic Fibrosis Patient-Derived Pseudomonas aeruginosa.Genetic engineering of Caulobacter crescentus for removal of cadmium from water.Expression of hcp in freshwater Synechococcus spp., a gene encoding a hyperconserved protein in picocyanobacteria.Biocidal performance of acrylated glyphosate in a model photopolymerizable coating formulation.Effects of increasing nitrogen and phosphorus concentrations on phytoplankton community growth and toxicity during Planktothrix blooms in Sandusky Bay, Lake Erie.Seasonal changes in microbial community structure and activity imply winter production is linked to summer hypoxia in a large lake.Self-immobilization of recombinant Caulobacter crescentus and its application in removal of cadmium from water.The decline and fate of an iron-induced subarctic phytoplankton bloom.A terrestrial origin for abundant riverine nanoscale ice-nucleating particlesPhysiological and biochemical response of freshwater cryptomonads (Cryptophyceae) to Fe deficiencyConstruction and initial characterization of a luminescent Synechococcus sp. PCC 7942 Fe-dependent bioreporterExpression of the iron-responsive irpA gene from the cyanobacterium Synechococcus sp strain PCC 7942Phycoerythrin is absent from the pyrenoid of Porphyridium cruentum: photosynthetic implicationsVERTICAL MIGRATION BY RHIZOSOLENIA SPP. (BACILLARIOPHYCEAE): IMPLICATIONS FOR FE ACQUISITIONMetatranscriptomic Analyses of Diel Metabolic Functions During a Microcystis Bloom in Western Lake Erie (United States)Ammonium recycling supports toxic Planktothrix blooms in Sandusky Bay, Lake Erie: Evidence from stable isotope and metatranscriptome dataScience meets policy: A framework for determining impairment designation criteria for large waterbodies affected by cyanobacterial harmful algal blooms
P50
Q30899150-57A48FF7-F5AB-4354-9C60-1F89340FC21EQ31144897-AF75E355-9BD7-4E39-8F06-F8F66D6E6E29Q33283170-2722DE94-403A-4D27-9873-811A90FBFB8AQ33922706-B865F56E-3B24-487A-8AAE-531B7D67D7B7Q34159972-95613E24-0F07-4788-BDDE-8001229516C3Q35167128-526ADD83-A796-40A6-A5B6-5D27693460B2Q35642048-4BAB7C19-8063-44B0-94D0-0CEE3EA10AF0Q35679021-553FF4E3-090C-4D4D-87FD-A37BF3C92540Q35725170-C1220D1B-7145-49F3-9430-F4ABE9B2E573Q36245854-C6BB6805-B56C-43FC-8312-2A7D776FE0F3Q37678996-07971709-5434-4224-B290-1FD0C4850FE9Q38680176-679E19AC-6A19-403B-A11F-D10FC16F68E3Q40002300-EC062E2D-8987-4042-B50F-90444041DF52Q40438064-F85F693E-11AF-420A-822E-117AED0F5721Q43367796-44A4D6A0-18B3-4902-90C0-3F54F3D1C1B8Q44856717-4C36927E-F54B-43B5-A40F-8BFAF52A19C0Q46226112-01728320-0135-4A23-9CE7-2200E8D1E5A7Q46726523-771BD8A9-3C02-44AF-B8AB-3B35E11D0842Q48036848-603C4A6E-17C8-4DCB-8A41-904DF2D7CF01Q50569568-424A10E5-7846-48B0-82EB-CC486C17E683Q51695194-CF59EB2A-D353-41E5-9B48-A88EC047B796Q57102608-54E93FF2-FBB3-4593-9778-FBD0398485EDQ73393527-D5BBA981-98DE-4F92-966A-960432635263Q74085300-6781E6DE-DB82-46D7-A6C1-9DD21716E9C2Q78865461-FFADE55D-7D56-4418-B861-5AC5A61AD072Q86671492-75F35288-4166-475C-9473-3F8155ACFA3CQ88063636-6E9443F8-8828-4E35-8DF5-3E5CCD2567FFQ90265624-39995BDC-245C-4A55-BDBD-AC4D85DD3AE0Q91026394-2CAF5AEC-D009-4543-A7FB-85FAC9A22373Q91026399-3B011786-880D-4A0F-AA7B-00AC0B24D505
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Robert M McKay
@nl
Robert M McKay
@sl
Robert M. McKay
@en
Robert M. McKay
@es
type
label
Robert M McKay
@nl
Robert M McKay
@sl
Robert M. McKay
@en
Robert M. McKay
@es
altLabel
Robert Michael McKay R Michael L McKay, R Michael McKay
@en
prefLabel
Robert M McKay
@nl
Robert M McKay
@sl
Robert M. McKay
@en
Robert M. McKay
@es
P108
P1053
P-3759-2017
P106
P1153
35556115500
P21
P2798
P31
P3829
P496
0000-0003-2723-5371