Alexander Wissemeier, Speyer DE
Alexander Wissemeier, Speyer DE
Patent application number | Description | Published |
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20100006015 | IRRIGATION SYSTEM AND METHOD FOR IRRIGATING OR FERTILIZING - A watering apparatus comprising a storage container having a tubular section which is closed with an open-cell foam based on an aminoplast, and a method for watering or applying fertilizer. | 01-14-2010 |
20100050514 | PLANT SUBSTRATE BASED ON OPEN-CELLED MELAMINE/FORMALDEHYDE FOAM - A plant substrate consisting of | 03-04-2010 |
20100218575 | PREPARATIONS WITH IMPROVED UREASE-INHIBITING EFFECT AND UREA-CONTAINING FERTILIZERS CONTAINING THE LATTER - The invention relates to preparations with improved urease-inhibitory effect which comprise at least two different (thio)phosphoric triamides and to urea-comprising fertilizers which comprise these preparations. The invention furthermore relates to a method of preparing these preparations, to the use of these preparations in the fertilization with urea-comprising fertilizers, and to the use of urea-comprising fertilizers which comprise these preparations in agriculture or in horticulture. | 09-02-2010 |
20110154874 | MIXTURE FOR THE TREATMENT OF UREA-CONTAINING FERTILIZERS - A mixture for the treatment of urea-containing fertilizers comprises a) at least one (thio)phosphoric acid triamide of the general formula (I) R | 06-30-2011 |
20120129696 | METHOD FOR INCREASING THE LEVEL OF FREE AMINO ACIDS IN STORAGE TISSUES OF PERENNIAL PLANTS - The present invention relates to method for increasing the level of free amino acids in storage tissues of perennial plants comprising the application of at least one strobilurin (compound A) selected from the group consisting of pyraclostrobin, orysastrobin, azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyribencarb, trifloxystrobin, 2-(2-(6-(3-chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl-acetamide, 3-15 methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclopropane-carboximidoylsulfanylmethyl)-phenyl)-acrylic acid methyl ester, methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)-ethyl]benzyl)carbamate and 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N-methyl-acetamide to the plant following the period of vegetative growth. In addition, the invention relates to the use of at least one strobilurin (compound A) selected from the group consisting of pyraclostrobin, orysastrobin, azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyribencarb, trifloxystrobin, 2-(2-(6-(3-chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl-acetamide, 3-15 methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclopropane-carboximidoylsulfanyl-methyl)-phenyl)-acrylic acid methyl ester, methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)-ethyl]benzyl)carbamate and 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N-methyl-acetamide for increasing the level of free amino acids in storage tissues of perennial plants. | 05-24-2012 |
20120252668 | Method for Reducing Nitrous Oxide Emission from Soils - The present invention relates to a method for reducing nitrous oxide emission from soils comprising treating a plant growing on the respective soil and/or the locus where the plant is growing or is intended to grow and/or the seeds from which the plant grows with at least one fungicide (compound A) and at least one ammonium- or urea-containing fertilizer (compound B) wherein the application of at least one compound (A) and at least one compound (B) is carried out with a time lag of at least 1 day. | 10-04-2012 |
20130012383 | USE OF AMINOCARBOXYLATES IN AGRICULTURE - Use of formulations comprising | 01-10-2013 |
20130017949 | Fungicidal Compositions Comprising a Phosphate Solubilizing Microorganism and a Fungicidally Active Compound - The present invention relates to a composition, comprising a microorganism as defined in the description and at least one compound (II) selected from groups A) to F) as defined in the description in a synergistically effective amount. | 01-17-2013 |