WO2013041665A1 - Method for cultivating sugar cane - Google Patents
Method for cultivating sugar cane Download PDFInfo
- Publication number
- WO2013041665A1 WO2013041665A1 PCT/EP2012/068625 EP2012068625W WO2013041665A1 WO 2013041665 A1 WO2013041665 A1 WO 2013041665A1 EP 2012068625 W EP2012068625 W EP 2012068625W WO 2013041665 A1 WO2013041665 A1 WO 2013041665A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- methyl
- buds
- phenyl
- iii
- growth
- Prior art date
Links
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- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- ZVUVJTQITHFYHV-UHFFFAOYSA-M potassium;naphthalene-1-carboxylate Chemical compound [K+].C1=CC=C2C(C(=O)[O-])=CC=CC2=C1 ZVUVJTQITHFYHV-UHFFFAOYSA-M 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- WHMZYGMQWIBNOC-UHFFFAOYSA-N propan-2-yl n-(3,4-dimethoxyphenyl)carbamate Chemical compound COC1=CC=C(NC(=O)OC(C)C)C=C1OC WHMZYGMQWIBNOC-UHFFFAOYSA-N 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- KQSJSRIUULBTSE-UHFFFAOYSA-M sodium;3-(3-ethylcyclopentyl)propanoate Chemical compound [Na+].CCC1CCC(CCC([O-])=O)C1 KQSJSRIUULBTSE-UHFFFAOYSA-M 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- UZKQTCBAMSWPJD-UQCOIBPSSA-N trans-Zeatin Natural products OCC(/C)=C\CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-UQCOIBPSSA-N 0.000 description 1
- UZKQTCBAMSWPJD-FARCUNLSSA-N trans-zeatin Chemical compound OCC(/C)=C/CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-FARCUNLSSA-N 0.000 description 1
- PIHCREFCPDWIPY-UHFFFAOYSA-N tris[2-(2,4-dichlorophenoxy)ethyl] phosphite Chemical compound ClC1=CC(Cl)=CC=C1OCCOP(OCCOC=1C(=CC(Cl)=CC=1)Cl)OCCOC1=CC=C(Cl)C=C1Cl PIHCREFCPDWIPY-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 229940023877 zeatin Drugs 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C1/00—Apparatus, or methods of use thereof, for testing or treating seed, roots, or the like, prior to sowing or planting
- A01C1/06—Coating or dressing seed
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C11/00—Transplanting machines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C21/00—Methods of fertilising, sowing or planting
Definitions
- the present invention relates to a method for cultivating sugar cane comprising removing buds together with meristematic tissue from the stalk of a 6 to 18 months old sugar cane plant, treating the buds with at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one rooting enabler and/or growth-promoting bacteria, planting these buds in a growth medium, growing seedlings from the buds at a temperature of at least 15°C, and 10 to 120 days after planting the buds, planting the seedlings grown from the buds to the field if the growth medium is not a field, or, in case the growth medium is a field, exposing the seedlings obtained from the buds to ambient conditions.
- sugar cane is one of the plants which are yet used for the production of biofuels (bioethanol) and is promising for further development, as the alcohol obtained by the fermentation of these plants provides a renewable and clean fuel.
- biofuels bioethanol
- the plantation area of sugar cane is increasing worldwide as well as the investments in factories to produce alcohol therefrom.
- the seed of sugar cane is a dry one-seeded fruit or caryopsis formed from a single carpel, the ovary wall (pericarp) being united with the seed-coat (testa). The seeds are ovate, yellowish brown and very small, about 1 mm long.
- the seed of sugar cane only germinates under specific environmental characteristics, such as a constant warm and humid climate conditions. Such climatic conditions are not found everywhere sugar cane is grown, and therefore germination of sugar cane seed is not always guaranteed.
- the seed of a sugar cane is not sown or planted, but instead, the cane is propagated vegetatively by planting a stem segment (or part of a stalk or culm or seedling).
- the stem of sugar cane, as well as the stem of graminaceous plants comprises several nodes, from which new plants grow.
- the traditional planting process of sugar cane involves the reservation of an area of the crop to be used as a source of plants for replanting, since the nodes are comprised in the stem.
- the plants used for replanting are harvested and then cut in segments of approximately 20 to 50 cm, so that at least 2 nodes are present in each stem segment (sett). Cutting the stems is needed to break apical dominance that otherwise causes poor germination when using full length (uncut) stems.
- the segments are cut to have at least 2 buds (or at least two nodes; every node gives generally rise to one single bud) to assure germination, because not every bud germinates.
- US 4,091 ,569 relates to a process for obtaining sound sugar cane gemmas for controlling the blight of sugar cane stumps left after cutting, comprising cutting transverse disc-shaped sections from the stalk containing gemmas, subjecting them to a heat treatment and then to a Benlate (benomyl) treatment, planting the treated gemmas into pre-germination beds and transplanting the scions grown therefrom to the field when they are about 30 cm high.
- Benlate benomyl
- the object is achieved by a method for cultivating sugar cane, which method comprises (i) removing buds together with meristematic tissue (in particular with a part of the node to which the buds are attached) from the stalk of a 6 to 18 months old sugar cane plant;
- carboxamide fungicide and/or at least one GABA antagonist insecticide and/or at least one nicotinic receptor agonist/antagonist insecticide and/or at least one chloride channel activator insecticide and optionally also with at least one fungicide different therefrom and/or at least one insecticide different therefrom and/or at least one nematicide and/or at least one growth regulator and/or at least one rooting enabler and/or growth-promoting bacteria in other words:
- At least one active agent selected from strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides, nicotinic receptor agonist/antagonist insecticides, chloride channel activator insecticides and mixtures thereof, and optionally also with at least one agent selected from fungicides different therefrom, insecticides different therefrom, nematicides, growth regulators, rooting enablers, growth-promoting bacteria and mixtures thereof);
- step (v) planting the buds obtained in step (ii), (iii) or (iv) in a growth medium;
- the medium is not a field, planting the seedlings obtained from the buds to the field, where the field has optionally been treated with at least one fertilizer and/or at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one superabsorber and/or growth-promoting bacteria before or during planting, or, in case the growth medium is a field, exposing the seedlings obtained from the buds to ambient conditions; and (x) optionally treating the seedlings and/or the field during or after planting in the field or after exposing to ambient conditions with at least one fertilizer and/or at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one superabsorber and/or growth-promoting bacteria and/or at least one freshness-preservation polymer.
- stem is the caulis or stalk of the culm part of a graminaceus plant (here: the sugar cane plant), i.e. the main trunk of a plant, specifically a primary plant axis that develops buds and shoots.
- Sett is a stem segment, section or cutting having one or more nodes.
- Node is the location in the stem where the shoot, bud or gemma is formed in a graminaceus plant (here: the sugar cane plant).
- Bus or “gemma” is the embryo, spore or germ of a plant (here: the sugar cane plant). It can also be defined as an undeveloped or embryonic shoot. A bud/gemma can be considered as the pre-stage of a shoot from which the latter develops when the bud leaves its dormant stage.
- a “removed bud” in the context of the present invention refers to a bud which also contains meristematic tissue.
- this term includes a bud plus a small section of the node to which it is attached. This term does however not encompass the whole node (with bud).
- the removed bud is a "bud chip", i.e. an essentially round or oval disc-shaped cutting of the stem containing the bud and some
- the term "bud” used in the description of the steps succeeding step (i) denotes the removed bud containing meristematic tissue, for example in form of a bud chip.
- “Seedling” is the young plant emerging/sprouting from propagation material, here from a bud. Within the terms of the present invention, the young plants are called
- step (ii), (ii) and (iv) are interchangeable. This means that the order in which these steps are carried out is not necessarily step (ii) followed by step (iii) followed by step (iv), but can be any sequence. Further details are given below. The following remarks made to preferred embodiments of the features of the method of the invention apply both alone as well as in particular in combination with each other.
- Step (i) is preferably carried out when the sugar cane plant is 8 to 12 months old.
- buds are removed from a sugar cane plant.
- the buds can be removed from the plant as it stands, but for practical reasons it is preferred to first remove the plant from the place where it is growing before removing the buds from the stalk.
- the top part of the stalk is cut off, so that the below, remaining stalk still comprises about 5 to 15, preferably 8 to 15 and in particular 8 to 12 nodes. This serves especially for removing inactive buds from the stalk and/or for facilitating the handling of the stalk in the subsequent bud removal step. For practical reasons it is preferred to cut off the top part of the stalk before the sugar cane plant is removed from the place where it is growing.
- Cutting off refers in the context of the present invention to any suitable procedure for removing the top part, such as cutting, chopping or sawing, e.g. with a knife, machete, axe, saw or any suitable machine, or by breaking off or tearing off manually the top part.
- the removal of the top part of the plant can be carried out manually or automatedly.
- step (i) the sugar cane plant is removed from the place where it is growing before the buds are removed, and before or after (preferably before) removing the sugar cane plant from the place where it is growing (and in any case before step the buds are removed), the top part of the stalk of the plant is cut off, so that the below stalk still comprises 5 to 15, preferably 8 to 15 and in particular 8 to 12 nodes.
- "Before” in this context means some days to a few seconds, e.g. three days to some seconds, before the plant is removed from the place where it is growing.
- the plant or its "decapitated" stalk can be removed together with its subterranean part. This can be carried out by any suitable means, such as eradicating, digging out or ploughing out the root. The removal can be carried out manually or automatedly. Subsequently, the (originally) subterranean part is preferably removed from the stalk. Removing the subterranean part from the stalk can be done by any suitable means, such as cutting or chopping it off or breaking or tearing it off mechanically, e.g.
- the plant/stalk is removed in such a manner that it comprises all nodes or at least 80% of the nodes present in the plant or in its "decapitated” stalk.
- Removing can be carried out by any suitable means, such as cutting, chopping or sawing, e.g. with a knife, machete, axe, saw or any suitable machine, or by breaking or tearing the stalk off mechanically, e.g. manually or by a kick.
- cutting, chopping or sawing e.g. with a knife, machete, axe, saw or any suitable machine, or by breaking or tearing the stalk off mechanically, e.g. manually or by a kick.
- the plant/stalk is removed by breaking or tearing it off mechanically, e.g. manually or, more practically, by a kick.
- This has the advantage that diseases possibly present in single plants are not spread to contaminate other, healthy plants via the tools used for cutting/chopping/sawing etc., such as knifes, machetes, axes, saws and the like.
- the time interval between removing the plant from the place where it is growing and removing the buds must not be too long in order to ensure that the buds are still productive.
- the maximum time interval can however be influenced by the storing conditions of the removed plant or its stalk. For instance, storage under humid conditions can prolong the maximum time interval.
- it is preferred to remove the buds shortly after the plant has been removed from the place where it has been growing e.g. at most 7 days, preferably at most 5 days, more preferably at most 3 days and in particular at most 2 days after the plant has been removed from the from the place where it has been growing.
- the buds are removed in such a way that the removed buds comprise meristematic tissue.
- the meristematic tissue is known to those skilled in the art and can be located by its position close to the node. The presence of meristematic tissue enables the removed buds to form roots and produce seedlings.
- the buds are removed close to the node from which they originate and preferably comprise (or, in other words, are attached to) a part of the node.
- the removal of the buds can be carried out by any suitable means, such as punching, cutting, chopping or sawing, e.g. with a knife, machete, axe, saw or any suitable machine, or by breaking off or tearing off manually the buds.
- the removal is preferably carried out by punching, e.g. with a suitable device, such as a manual or automated punching machine.
- the stalks, before removing the buds are cut lengthwise (longitudinally) in such a way that the buds are as centralized as possible on the resulting two halves of the stalk.
- buds or stalk pieces containing the buds e.g. disks with a diameter of about 1 to 5 cm, preferably 1 to 3 cm, more preferably 2 to 3 cm, containing the buds and a part of the node, are removed, e.g. by cutting, sawing or punching, punching being preferred.
- Punching can be carried out by a punching machine, such as the Sugarcane Bud Extractor from Copersucar, Brazil.
- step (ii) the buds obtained in step (i) or (iii) or (iv) are subjected to a sterilization treatment. This treatment is carried out for destroying harmful
- microorganisms such as bacteria and viruses, which may be harmful to the bud or the plant developing therefrom, such as the microorganism causing ratoon stunting disease.
- Sterilization can be carried out by any means known for destroying microorganisms.
- the sterilization treatment must not deteriorate the buds or impair their germination ability. Suitable sterilization treatments are for example heat treatment, treatment with an alcohol solution, treatment with a hypochlorite solution or ⁇ -irradiation or a combination of these methods.
- the heat treatment is preferably carried out by means of water or steam having a temperature of at least 50°C, e.g. 50 to 60°C or 50 to 55°C, preferably of at least 51 °C, e.g. 51 to 60°C or 51 to 55°C, and especially of ca. 52°C.
- the buds are for example immersed into water or doused or spilled or sprinkled or sprayed with water of the desired temperature or are surrounded by steam of the desired temperature (if required at reduced pressure).
- the heat treatment is preferably carried out for 5 minutes to 4 hours, preferably for 10 minutes to 2 hours.
- the duration of the heat treatment generally depends from the applied temperature; the higher the applied temperature, the shorter being the time. For instance, if the applied temperature is ca. 50°C, application time is preferably ca. 2 h, and if the applied temperature is ca. 52°C, application time is preferably ca.
- the alcohol treatment is preferably carried out by contacting the buds with an alcohol solution, for example by immersing the buds into an alcohol solution, preferably into an aqueous ca. 70% ethanol solution, or by spilling or sprinkling or spraying the buds with such a solution.
- the hypochlorite treatment is preferably carried out by contacting the buds with an aqueous hypochlorite solution, for example by immersing the buds into an aqueous hypochlorite solution, preferably into an aqueous sodium or potassium hypochlorite solution, such as Eau de Javel, in a concentration of preferably from 0.1 to 1 %, more preferably from 0.1 to 0.5%.
- ⁇ -irradiation is preferably carried out by exposing the buds to a ⁇ source.
- preference is given to the heat treatment.
- step (iii) the buds obtained in step (i) or (ii) or (iv) are treated with at least one
- strobilurin fungicide and/or at least one carboxamide fungicide and/or at least one GABA antagonist insecticide and/or at least one nicotinic receptor agonist/antagonist insecticide and/or at least one chloride channel activator insecticide i.e. with at least one active agent selected from strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides, nicotinic receptor agonist/antagonist insecticides and chloride channel activator insecticides.
- fungicides different therefrom and/or at least one insecticide different therefrom and/or at least one nematicide and/or at least one growth regulator and/or at least one rooting enabler and/or growth-promoting bacteria are described below.
- At least one fungicide different from strobilurins at least one insecticide and/or at least one nematicide are carried out depends among others on the (type and intensity of) pest pressure. This treatment is carried out for protecting the buds from diseases and pests, but also for supporting physiological effects.
- the at least one strobilurin fungicide is selected from azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyraoxystrobin, pyrametostrobin, pyribencarb, trifloxystrobin, 2-(2-(6-(3-chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4- yloxy)-phenyl)-2-methoxyimino-N-methyl-acetamide, 3-methoxy-2-(2-(N-(4-methoxy- phenyl)-cyclopropane-carboximidoylsulfanylmethyl)-phenyl)-acrylic acid methyl ester,
- azoxystrobin dimoxystrobin, fluoxastrobin, fluxapyroxade, kresoxim-methyl, orysastrobin, picoxystrobin, pyraclostrobin and trifloxystrobin.
- the strobilurin fungicide is pyraclostrobin.
- the at least one carboxamide fungicide [i.e. the carboxamide fungicide used in step (iii), but also preferably used in the optional treatment steps] is selected from benalaxyl, benalaxyl-M, benodanil, bixafen, boscalid, carboxin, fenfuram, fenhexamid, flutolanil, furametpyr, isopyrazam, isotianil, kiralaxyl, mepronil, metalaxyl, metalaxyl-M (mefenoxam), ofurace, oxadixyl, oxycarboxin, penthiopyrad, sedaxane, tecloftalam, thifluzamide, tiadinil, 2-amino-4-methyl-thiazole-5-carboxanilide, 2-chloro-N-(1 ,1 ,3- trimethyl-indan-4-yl)-nic
- the at least one GABA antagonist i.e. the GABA antagonist insecticide used in step (iii), but also preferably used in the optional treatment steps] is selected from acetoprole, endosulfan, vaniliprole, pyrafluprole, pyriprole, the phenylpyrazole compound of the formula II where R a is Ci-C4-alkyl or Ci-C4-haloalkyl;
- the GABA antagonist insecticide is selected from fipronil.
- the at least one nicotinic receptor agonist/antagonist insecticide i.e. the nicotinic receptor agonist/antagonist insecticide used in step (iii), but also preferably used in the optional treatment steps
- the at least one nicotinic receptor agonist/antagonist insecticide is selected from acetamiprid, bensultap, cartap hydrochloride, clothianidin, dinotefuran, imidacloprid, thiamethoxam, nitenpyram, nicotine, spinosad (allosteric agonist), spinetoram (allosteric agonist), thiacloprid, thiocyclam, thiosultap-sodium and AKD1022.
- the at least one nicotinic receptor agonist/antagonist insecticide is selected from acetamiprid, clothianidin, imidacloprid and thiamethoxam and is specifically thiamethoxam.
- the at least one chloride channel activator insecticide i.e. the chloride channel activator insecticide used in step (iii), but also preferably used in the optional treatment steps] is selected from abamectin, emamectin, ivermectin, lepimectin and milbemectin. More preferably, the at least one chloride channel activator insecticide is abamectin.
- the buds are treated in step (iii) with at least one strobilurin fungicide. Suitable and preferred strobilurin fungicides are listed above.
- the buds are treated in step (iii) with at least one carboxamide fungicide.
- carboxamide fungicides are listed above.
- the buds are treated in step (iii) with at least one GABA antagonist insecticide.
- GABA antagonist insecticides are listed above.
- the buds are treated in step (iii) with al least one nicotinic receptor agonist/antagonist insecticide.
- al least one nicotinic receptor agonist/antagonist insecticide are listed above.
- the buds are treated in step (iii) with at least one chloride channel activator insecticide.
- chloride channel activator insecticides are listed above.
- Suitable and preferred chloride channel activator insecticides are listed above.
- strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides and nicotinic receptor agonist/antagonist insecticides are listed above.
- step (iii) is preferably carried out by bringing the buds into contact with at least one of the above-listed active agents, preferably with a liquid medium containing the active agent(s), more preferably with a solution thereof, even more preferably an aqueous solution thereof.
- "Bringing into contact” can be carried out by any suitable means known for example from seed treatment, such as immersing, dousing, sprinkling, spraying, dipping, coating, dressing and the like. The choice of the technique will depend on the available means, on the active agent, but also on the desired duration and intensity of contact.
- the treatment may be carried out by mixing the buds with the particular amount desired of active ingredient formulations either as such or after prior dilution with water in an apparatus suitable for this purpose, for example a mixing apparatus for solid or solid/liquid mixing partners, until the composition is distributed uniformly on the buds. If appropriate, this can be followed by a drying operation.
- an apparatus suitable for this purpose for example a mixing apparatus for solid or solid/liquid mixing partners
- immersing the buds into a solution containing one or more active agents is immersing the buds into a solution containing one or more active agents.
- the suitable duration of contact depends on several factors, such as the treatment technique, the specific active agent, its concentration in solution and the health status of the buds, and can be determined by those skilled in the art for each particular case. For instance, immersing can last from a few seconds to 10 minutes, preferably from 3 seconds to 5 minutes, more preferably from 5 seconds to 1 minute. Dousing, sprinkling, spraying and dipping can be carried out to run-off point.
- the above-mentioned techniques are preferably carried out in such a way that the whole bud (including the meristematic tissue bound thereto) is brought into contact with the active agent or the medium containing the active agent, be it for example by complete immersion, dousing, sprinkling or spraying on the complete surface of the bud to run-off point and the like.
- the buds are preferably treated in step (iii) with the at least one active agent selected from strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides, nicotinic receptor agonist/antagonist insecticides, chloride channel activator insecticides and mixtures thereof by immersing the complete bud into a liquid medium containing said active agent.
- the active agents used in step (iii) are preferably brought into contact with the buds in form of an aqueous solution.
- the aqueous solution contains the active agents, especially the strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides, nicotinic receptor agonist/antagonist insecticides and/or chloride channel activator insecticides, in a concentration of from 0.001 to 10% by weight, more preferably from 0.01 to 5% by weight, even more preferably from 0.05 to 1 % by weight and in particular from 0.05 to 0.5% by weight, relative to the weight of the solution.
- the active agents especially the strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides, nicotinic receptor agonist/antagonist insecticides and/or chloride channel activator insecticides, in a concentration of from 0.001 to 10% by weight, more preferably from 0.01 to 5% by weight, even more preferably from 0.05 to 1 % by weight and in particular from 0.05 to 0.5% by weight, relative to the weight of the solution.
- the aqueous solution used in step (iii) contains the active agent(s) in an amount of from 0.01 to 100 g/l of solution, more preferably from 0.1 to 50 g/l of solution, even more preferably from 0.5 to 10 g/l of solution and in particular from 0.5 to 5 g/l of solution.
- step (iv) the buds obtained in step (i), (ii) or (iii) are refrigerated.
- Refrigerating in this context means cooling the buds to a temperature of from 0°C to 14°C, preferably from 3°C to 10°C and in particular from 5 to 8°C.
- This refrigerating step serves especially for storing the buds if planting or the treatment of steps (ii) and/or (iii) cannot be carried out shortly after removing them from the stalk or if they are to be transported to be stored and/or planted in a remote place.
- the refrigerating lasts preferably at most 1 month, more preferably at most 15 days.
- steps (ii), (ii) and (iv) are interchangeable. This means that the order in which these steps are carried out is variable. The only prerequisite is that they are carried out after step (i) and before step (v) and that step (iii) is carried out mandatorily, while steps (ii) and (iv) are optional. Suitable sequences are for example:
- step (ii) followed by step (iii)
- step (iii) followed by step (ii)
- step (iii) followed by step (iv)
- step (iv) followed by step (iii)
- step (ii) followed by step (iii) followed by step (iv)
- step (ii) followed by step (iv) followed by step (iii)
- step (iii) followed by step (iv) followed by step (ii)
- step (iii) followed by step (iv)
- step (iv) followed by step (iii).
- steps (ii), (iii) or (iv) are then planted in a growth medium [step (v)].
- the growth medium may be a natural or synthetic substrate or a mixture thereof.
- the growth medium may also be a nutrient solution, such as an aqueous solution containing growth factors, fertilizers, buffers, ion exchangers, inorganic salts, such as calcium salts (e.g. calcium nitrate, calcium sulphate, calcium hydrogen phosphate), magnesium salts (e.g.
- magnesium nitrate, magnesium sulphate potassium salts (e.g. potassium dihydrogen phosphate, potassium nitrate), iron salts (e.g. ferrous sulfate, ferric chloride) and micronutrients (e.g. lithium salts, such as lithium chloride, copper salts, such as copper sulfate, zinc salts, such as zinc sulfate, aluminium salts, such as aluminium sulfate, nickel salts, such as nickel sulfate, tin salts, such as tin chloride, cobalt salts, such as cobalt nitrate, boric acid) and mixtures thereof like Knop's nutrition solution and Hoagland's A-Z solution, and the like.
- the nutrient solution may be form-stabilized, e.g. by an inorganic substrate, such as expanded clay. More preferably the growth medium is however sand, vermiculite or coconut fibers, specifically coconut fibers.
- the growth medium may be treated before, during and/or after planting the buds with at least one fertilizer and/or at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one superabsorber and/or growth-promoting bacteria.
- Suitable and preferred fertilizers, fungicides, insecticides, nematicides, growth regulators, superabsorbers and growth-promoting bacteria are described below.
- the fungicides especial preference is given to the treatment with fungicides which also have a physiological, especially a plant health and/or growth-promoting effect, such as the strobilurins and especially pyraclostrobin.
- Preferred is the treatment with at least one fungicide, in particular a strobilurin fungicide, especially pyraclostrobin, and/or at least one growth regulator.
- step (vi) is carried out.
- the growth medium is treated with at least one strobilurin fungicide and optionally also with at least one fungicide different therefrom and/or at least one fertilizer and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one superabsorber and/or growth-promoting bacteria.
- Suitable and preferred strobilurin fungicides are listed above and below. Specific preference is given to pyraclostrobin.
- the buds are planted in a container containing a growth medium. Suitable growth media are listed above.
- Preferred growth media to be used in a container are selected from sand, vermiculite, coconut fibers and mixtures thereof and are more preferably vermiculite or coconut fibers, specifically coconut fibers.
- the container may be made of a conventional material or a biodegradable material.
- Biodegradable containers have the advantage that the seedling can be planted together with the container into the field, i.e. there is no need to remove the seedling from the container before planting. This in turn has the advantage that planting can be carried out using an automatic or semi-automatic planting machine.
- a biodegradable container is used in step (v).
- the biodegradable container is based on a biodegradable material which in turn is preferably based on biodegradable polyesters, starch, cellulose, cellulosic material, polylactic acid, caoutchouc, paper, paperboard, pulp of cellulosic origin, straw, bagasse, sawdust, natural fibres or mixtures thereof.
- the container is a conventional (i.e. not specifically biodegradable) one.
- seedlings are grown from the buds at a temperature of at least 15°C.
- seedlings are grown from the buds at a temperature of from 15 to 35°C.
- seedlings are grown from the buds at a temperature of at least 18°C, even more preferably from 18 to 35°C, particularly preferably from 20 to 35°C, in particular from 22 to 35°C and especially from 25 to 35°C, e.g. 25 to 32°C or 25 to 30°C or 25 to 28°C or 25 to 27°C.
- seedlings are grown from the buds at a humidity of from 40 to 100%, more preferably from 50 to 95%, even more preferably from 70 to 90% and in particular from 70 to 80%.
- the required temperature is realized either naturally, for instance if the seedlings are grown from the buds in a warm climate, e.g. in a tropical climate, or by the aid of artificial means.
- Artificial means are for example greenhouses or covering materials.
- the growing medium may for example be in a greenhouse or be transferred thereto after planting, or the growing medium containing the bud may be thermally insulated, e.g. by covering with a suitable material, such as a foil.
- the buds are planted into a container containing a growth medium, where the container is in a greenhouse or is placed into a greenhouse after planting.
- the temperature is preferably in the range of from 15 to 35°C, more preferably from 18 to 35°C, even more preferably from 20 to 35°C, in particular from 22 to 35°C and especially from 25 to 35°C, e.g. 25 to 32°C or 25 to 30°C or 25 to 28°C or 25 to 27°C.
- Humidity is preferably in the range of from 40 to 100%, more preferably from 50 to 95%, even more preferably from 70 to 90% and in particular 70 to 80%.
- the buds are planted into a container containing a growth medium or into a field (in this case the growth medium is the soil of the field) and the container or the field is covered with one or more covering materials.
- Covering materials are for example textile mats and cover foils customarily used for thermal insulation/protection in agriculture, such as agriculture plastic foil, preferably black foil, for example in the form of foil tunnels, or fleece mats.
- step (viii) the seedlings, while growing at a temperature of at least 15°C, and/or their growth medium are treated once or several times, e.g. 1 , 2 or 3 times, preferably once or twice, with at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one rooting enabler and/or growth-promoting bacteria.
- Suitable and preferred fungicides, insecticides, nematicides, growth regulators, rooting enablers and growth-promoting bacteria are described above and below. Treating the seedling means in this context that either the seedling, when emerged from the growth medium, or the growth medium or both are treated. If treatments with at least one fungicide, at least one insecticide and/or at least one nematicide are carried out depends among others on the (type and intensity of) pest pressure.
- step (viii) is carried out, i.e. it is preferably not optional, but mandatory.
- the seedlings, while growing, and/or their growth medium are treated with at least one strobilurin fungicide and/or at least one carboxamide fungicide and/or at least one GABA antagonist insecticide and/or at least one nicotinic receptor
- agonist/antagonist insecticide and/or at least one chloride channel activator insecticide and optionally also with at least one nematicide and/or at least one growth regulator and/or at least one rooting enabler and/or growth-promoting bacteria.
- Suitable and preferred nematicides, growth regulators, rooting enablers and growth-promoting bacteria are described above and below.
- the seedlings, while growing, and/or their growth medium are treated with at least one strobilurin fungicide.
- the seedlings, while growing, and/or their growth medium are treated with at least one carboxamide fungicide.
- the seedlings, while growing, and/or their growth medium are treated with at least one GABA antagonist insecticide.
- the seedlings, while growing, and/or their growth medium are treated with at least one nicotinic receptor agonist/antagonist insecticide. In an alternatively preferred embodiment, the seedlings, while growing, and/or their growth medium are treated with at least one chloride channel activator insecticide.
- the seedlings, while growing, and/or their growth medium are treated with at least one strobilurin fungicide and at least one GABA antagonist insecticide.
- Suitable and preferred strobilurin fungicides, carboxamide fungicides, GABA antagonist insecticides, nicotinic receptor agonist/antagonist insecticides and chloride channel activator insecticides correspond to those listed above for step (iii).
- the seedling which has grown from the bud is planted to the field (of course only if the growth medium is not yet a field).
- the seedling has generally a length of from 20 to 80 cm. Planting to the field is more preferably carried out 20 to 80 days, even more preferably 25 to 70 days, in particular 25 to 60 days and specifically 30 ⁇ 5 days after having planted the bud in the growth medium.
- the seedlings, before being planted to the field are allowed to acclimatize, i.e. they are allowed to adapt to conditions as they are present in the field.
- they can for example be brought into an area with weather conditions similar or identical to the conditions in the field, i.e. with changes in temperature, humidity, rain, drought etc, or the roof of the glass house can be partially or completely removed.
- This acclimatization is generally carried out 1 day to 1 month, preferably 1 day to 3 weeks, more preferably 10 to 20 days before planting to the field.
- the field has optionally been treated with at least one fertilizer and/or at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one superabsorber and/or growth-promoting bacteria before planting.
- These treatments can also be carried out during planting, for instance in the form of an in-furrow application.
- Suitable and preferred fertilizers, fungicides, insecticides, nematicides, growth regulators, superabsorbers and growth- promoting bacteria are described below. Planting into the field may take place manually, semi-automatically or automatedly.
- Planting can for example take place totally automatedly if biodegradable containers are used for planting the buds and growing the seedlings therein.
- the seedlings needn't be taken out of the containers before planting, which allows the use of a planting machine for the whole process of planting.
- the seedlings have to be taken out the container before planting, which is generally carried out manually. Planting can then take place automatedly.
- planting to the field is carried out automatedly (mechanical planting), i.e. using a planting machine.
- Mechanical planting with a semiautomatic or automatic planting machine allows a very regular planting, e.g. very linear (in one line with only small deviations from linearity) and also essentially equidistant (equidistance between the planted seedlings).
- Semiautomatic or automatic planting machines moreover plant the seedlings with the correct orientation, i.e. with the aerial parts upturned and the roots downturned. This leads to a more regular, linear tillering of the plants.
- Linearity of the planted rows, equidistance of the plants and/or regular/linear tillering in turn ease harvesting of the sugar cane plants grown from the mechanically planted seedlings, especially harvesting with a harvesting machine, and thus eventually enhance the yield because less stalks remain uncut or maimed due to their deviation from linearity or equidistance or erratic tillering.
- Especially maimed stalks may damage the plant or its roots and be a source for diseases.
- the field is the growth medium, 10 to 120, preferably 20 to 100, more preferably 20 to 80 days, even more preferably 25 to 70 days, in particular 25 to 60 days and specifically 30 ⁇ 5 days after having planted the bud, the seedling grown therefrom is exposed to ambient conditions, i.e. is no longer protected thermally.
- a covering material such as a cover foil or a fleece mat, this is removed.
- the seedlings are optionally pruned.
- the seedling or the field may be treated with at least one fertilizer and/or at least one fungicide and/or at least one insecticide and/or at least one nematicide and/or at least one growth regulator and/or at least one superabsorber and/or growth-promoting bacteria and/or at least one freshness-preservation polymer.
- Suitable and preferred fertilizers, fungicides, insecticides, nematicides, growth regulators, superabsorbers, growth- promoting bacteria and freshness-preservation polymers are described below.
- step (iii) the at least one fungicide [to be more precise, the at least one fungicide optionally used in step (iii),
- A) azoles selected from the group consisting of
- azoxystrobin dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, meto- minostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyraoxystrobin, pyrametostrobin, pyribencarb, trifloxystrobin, 2-(2-(6-(3-chloro-2-methyl-phen- oxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl-acetamide, 3-methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclopropane-carboximidoyl- sulfanylmethyl)-phenyl)-acrylic acid methyl ester, methyl (2-chloro-5-[1 -(3- methylbenzyloxyimino)ethyl]benzyl)carbamate and 2-(2-(3-(
- antibiotics kasugamycin, kasugamycin hydrochloride-hydrate, streptomycin, polyoxine, validamycin A;
- nitrophenyl derivates binapacryl, dinobuton, dinocap, meptyldinocap, nitrthal- isopropyl, tecnazen,
- organometal compounds fentin salts, such as fentin-acetate, fentin chloride or fentin hydroxide;
- organophosphorus compounds edifenphos, fosetyl, fosetyl-aluminum, iprobenfos, phosphorous acid and its salts, pyrazophos, tolclofos-methyl;
- organochlorine compounds chlorothalonil, dichlofluanid, dichlorophen, flusulfamide, hexachlorobenzene, pencycuron, pentachlorphenole and its salts, phthalide, quintozene, thiophanate-methyl, tolylfluanid, N-(4-chloro-2-nitro- phenyl)-N-ethyl-4-methyl-benzenesulfonamide;
- inorganic active substances Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur;
- Biological control is defined as the reduction of pest population by natural enemies and typically involves an active human role.
- the biological control of plant diseases is most often based on an antagonistic action of the BCA.
- fungicidal biocontrol is thought to work, including the production of antifungal antibiotics, competition for nutrients and rhizosphere colonization.
- Suitable biological control agents are selected from non-pathogenic bacteria, preferably selected from Pseudomonas fluorescens, Pseudomonas putida.
- Streptomyces griseus Streptomyces ochraceisleroticus, Streptomyces graminofaciens, Streptomyces corchousii, Streptomyces spiroverticillatus, Streptomyces griseovirdis, Streptomyces hygroscopicus, Bacillus subtilis, Bacillus cereus, Bacillus mycoides, Bacillus pumilus, Bacillus licheniformis, Bacillus thuringensis, and metabolites produced from said bacteria; non-pathogenic fungi, preferably selected from Trichoderma spp.,
- Trichoderma harzianum Trichoderma viridae, Verticillium lecanii, Sporidesmium sclerotiorum and Zygomycetes, and metabolites produced from said fungi; resin acids; plant extracts of Reynoutria sachalinensis; and plant defence induction agents, preferably harpin.
- the at least one fungicide is selected from cyproconazole,
- the at least one fungicide is a strobilurin fungicide or is a carboxamide fungicide or is Bacillus subtilis and/or its metabolites or is a combination of at least two of these fungicides.
- Preferred strobilurins are selected from azoxystrobin,
- dimoxystrobin dimoxystrobin, fluoxastrobin, fluxapyroxade, kresoxim-methyl, orysastrobin,
- the strobilurin fungicide is pyraclostrobin.
- Preferred carboxamide fungicides are boscalid and fluxapyroxade and specifically fluxapyroxade.
- the at least one insecticide [to be more precise, the at least one insecticide optionally used in step (iii), (vi), (viii), (ix) and/or (x)] is preferably selected from
- pyrethroid compounds selected from acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cylclopentenyl,
- GABA gated chloride channel antagonist compounds selected from
- R a is Ci-C4-alkyl or Ci-C4-haloalkyl
- the at least one insecticide is selected from fipronil, acetamiprid, chlothianidin, imidacloprid, thiamethoxam, abamectin and teflubenzuron, even more preferably from fipronil and thiamethoxam and is specifically fipronil.
- the at least one nematicide is preferably selected from
- antibiotic nematicides such as abamectin
- botanical nematicides such as carvacrol
- carbamate nematicides selected from benomyl, carbofuran, carbosulfan and
- - oxime carbamate nematicides selected from alanycarb, aldicarb, aldoxycarb, oxamyl and tirpate; - fumigant nematicides selected from dithioether and methyl bromide; organophosphorus nematicides: - organophosphate nematicides selected from diamidafos; fenamiphos; fosthietan and phosphamidon;
- organothiophosphate nematicides selected from cadusafos, chlorpyrifos,
- dichlofenthion dimethoate, ethoprophos, fensulfothion, fosthiazate, heterophos, isamidofos, isazofos, phorate, phosphocarb, terbufos, thionazin and triazophos;
- nematicides selected from acetoprole, benclothiaz, chloropicrin, dazomet, DBCP, DCIP, 1 ,2-dichloropropane, 1 ,3-dichloropropene, fluensulfone, furfural, metam, methyl iodide, methyl isothiocyanate and xylenols.
- the at least one nematicide is abamectin.
- the growth-promoting bacteria are preferably selected from bacteria of the genera azospirillum, azotobacter, azomonas, bacillus, beijerinckia, burkholderia, Clostridium, cyanobacteria, enterobacter, erwinia, gluconobacter, klebsiella and streptomyces. More preferably, the growth-promoting bacteria are selected from Azospirillum amazonense, Herbaspirillum seropedicae, Herbaspirillum rubrisubalbicans,
- Burkholderia tropica Gluconacetobacter diazotrophicus, Pseudomonas fluorescens, Pseudomonas putida. Streptomyces griseus, Streptomyces ochraceisleroticus, Streptomyces graminofaciens, Streptomyces corchousii, Streptomyces
- the at least one growth regulator is preferably selected from acylcyclohexanediones, such as prohexadione, prohexaione-Ca, trinexapac or trinexapac ethyl; mepiquat chloride and chlormequatchloride. More preferably, the at least one growth regulator is selected from acylcyclohexanediones, such as prohexadione, prohexaidone-Ca, trinexapac or trinexapac ethyl, and in particular from prohexaidone-Ca and trinexapac ethyl.
- the at least one rooting enabler is preferably selected from the above strobilurin fungicides, in particular fluxapyroxade and pyraclostrobin, the above nicotinic receptor agonists/antagonists, in particular clothianidin, imidacloprid and thiamethoxam, auxins, such as 4-CPA, 2,4-D, 2,4-DB, 2,4-DEP, dichlorprop, fenoprop, IAA, IBA,
- naphthaleneacetamide a-naphthaleneacetic acid, 1 -naphthol, naphthoxyacetic acids, potassium naphthenate, sodium naphthenate and 2,4,5-T
- gibberellins gibberellic acid
- cytokinins such as 2iP, benzyladenine, 4-hydroxyphenethyl alcohol, kinetin and zeatin
- humic acids extracts of Quillaja or Gleditsia, saponines, biological control agents and plant defence induction agents.
- Suitable fertilizers are those customarily used in the cultivation of sugar cane plants, such as NPK fertilizers, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, products of vegetable origin, such as cereal meal, tree bark meal, wood meal, nutshell meal and mulch, and mixtures thereof.
- the at least one superabsorber is preferably a superabsorbent polymer having an absorption capacity for deionised water of least 100 g/1 g of polymer.
- Superabsorbent polymers are well-known synthetic organic polymers which are solid and hydrophilic, which are insoluble in water, and which are capable of absorbing a multiple of their weight of water or aqueous solutions, thereby forming a water containing polymer gel. They may be nonionic or ionic crosslinked polymers. Suitable superabsorbent polymers are for example known from US 4,417,992, US 3,669,103, WO 01/25493 and
- WO 2008/031870 They are also commercially available, e.g. from SNF SA., France, under the trademark Aquasorb®, e.g. 3500 S, or from BASF SE under the trade names Luquasorb®, e.g. Luquasorb® 1010, Luquasorb® 1280, Luquasorb® 1060,
- Luquasorb® 1 160 Luquasorb® 1061 and HySorb®.
- fungicides, insecticides, nematicides, growth regulators and rooting enablers are generally used as ready-to-use preparations.
- suitable ready-to-use preparations containing at least one fungicide, insecticide, nematicide, growth regulator or rooting enabler are described.
- the active ingredient can be present in suspended, emulsified or dissolved form.
- the application forms depend entirely on the intended uses.
- the active ingredient can be applied as such, in the form of its formulations or the application form prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, including highly concentrated aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, compositions for broadcasting or granules.
- Application is for example by spraying, immersing, dousing, sprinkling, spraying, dipping, coating, dressing, atomizing, dusting, broadcasting or watering.
- the application forms and methods depend on the intended uses; in each case, they should ensure the finest possible distribution of the active compounds.
- suitable and preferred application techniques of the active agents mandatorily used in step (iii) reference is made to the above remarks.
- ready-to-use preparations of the active ingredient comprise one or more liquid or solid carriers, if appropriate surfactants and if appropriate further auxiliaries customary for formulating crop protection agents.
- the recipes for such formulations are familiar to the person skilled in the art.
- Aqueous application forms can be prepared, for example, from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by addition of water.
- the active compounds as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier.
- a wetting agent e.g., tackifier, dispersant or emulsifier
- concentrates composed of active substance, wetting agent, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, such concentrates being suitable for dilution with water.
- concentrations of the active ingredient in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are between 0.0001 and 10%, preferably between 0.01 and 1 % (% by weight total content of active compound, based on the total weight of the ready-to-use preparation).
- the active ingredient may also be used successfully in the ultra-low-volume process (ULV), it being possible to employ formulations comprising more than 95% by weight of active compound, or even to apply the active ingredient without additives.
- UUV ultra-low-volume process
- Oils of various types, wetting agents, adjuvants, bactericides and/or fertilizers may be added to the active ingredient, even, if appropriate, not until immediately prior to use (tank mix). These agents can be mixed in a weight ratio of from 1 :100 bis 100:1 , preferably from 1 :10 to 10:1 with the active ingredient employed.
- Adjuvants are for example: modified organic polysiloxanes, e.g. Break Thru S 240 ® ; alkohol alkoxylates, e.g. Atplus 245 ® , Atplus MBA 1303 ® , Plurafac LF 300 ® and Lutensol ON 30 ® ; EO-PO block copolymers, e.g.
- Pluronic RPE 2035 ® and Genapol B ® alkohol ethoxylates, e.g. Lutensol XP 80 ® ; and sodium dioctylsulfosuccinate, e.g.
- Leophen RA ® Leophen RA ® .
- the formulations are prepared in a known manner, for example by extending the active ingredient with solvents and/or carriers, if desired with the use of surfactants, i.e.
- Solvents/carriers suitable for this purpose are essentially: water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, methyl hydroxybutyl ketone, diacetone alcohol, mesityl oxide, isophorone), lactones (for example gamma-butyrolactone), pyrrolidones (pyrrolidone,
- aromatic solvents for example Solvesso products, xylene
- paraffins for example mineral oil fractions
- alcohols for example methanol, butanol, pentanol, benzyl alcohol
- ketones for example cyclohexanone, methyl hydroxybutyl ketone, diacetone alcohol, mesityl oxide, isophorone
- lactones for example gamma-butyrolactone
- N-methylpyrrolidone N-ethylpyrrolidone, n-octylpyrrolidone
- acetates glycols
- dimethyl fatty acid amides fatty acids and fatty acid esters.
- solvent mixtures may also be used.
- Carriers such as ground natural minerals (for example kaolins, clays, talc, chalk) and ground synthetic minerals (for example finely divided silica, silicates); emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates), and dispersants such as lignosulfite waste liquors and methylcellulose.
- ground natural minerals for example kaolins, clays, talc, chalk
- ground synthetic minerals for example finely divided silica, silicates
- emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates)
- dispersants such as lignosulfite waste liquors and methylcellulose.
- Suitable surfactants are alkali metal salts, alkaline earth metal salts and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid,
- dibutylnaphthalenesulfonic acid alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with
- formaldehyde condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenyl polyglycol ether, tributylphenyl polyglycol ether, tristerylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.
- Suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable and animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin,
- Powders, compositions for broadcasting and dusts can be prepared by mixing or jointly grinding the active ingredient with a solid carrier.
- Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredient onto solid carriers.
- Solid carriers are, for example, mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and plant products such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powder and other solid carriers.
- mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium
- Formulations for bud treatment can further comprise binders and/or gelling agents and optionally colorants.
- the formulations comprise between 0.01 and 95% by weight, preferably between 0.1 and 90% by weight, in particular 5 to 50% by weight, of the active ingredient.
- the active ingredient is employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
- formulations for bud treatment may comprise 0.01 to 60% by weight, preferably 0.1 to 40% by weight of the active ingredient in the ready-to-use preparations.
- formulations are: 1 . Products for dilution in water
- Water-soluble concentrates (SL, LS) 10 parts by weight of active compound are dissolved in 90 parts by weight of water or a water-soluble solvent. Alternatively, wetting agents or other adjuvants are added. Upon dilution in water, the active compound dissolves. The ready formulation contains 10% by weight of active ingredient.
- active compound 20 parts by weight of active compound are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone.
- a dispersant for example polyvinylpyrrolidone.
- the active ingredient is contained in 20% by weight. Upon dilution in water, a dispersion results.
- Emulsions (EW, EO, ES)
- active compound 25 parts by weight of active compound are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
- This mixture is introduced into 30 parts by weight of water by means of an emulsifier (Ultraturrax) and made into a homogeneous emulsion.
- the active ingredient is contained in 25% by weight. Upon dilution in water, an emulsion results.
- active compound 20 parts by weight of active compound are comminuted in a stirred ball mill with addition of 10 parts by weight of dispersants, wetting agents and 70 parts by weight of water or an organic solvent to give a fine suspension of active compound.
- the active ingredient is contained in 20% by weight. Upon dilution in water, a stable suspension of the active compound results.
- active compound 75 parts by weight of active compound are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetting agents and silica gel.
- the active ingredient is contained in 75% by weight. Upon dilution in water, a stable dispersion or solution of the active compound results.
- compositions suitable for treating the buds are, for example:
- IX dusts and dust-like powders Preferred formulations to be used for bud treatment are FS formulations.
- theses formulations comprise 1 to 800 g/l of active compounds, 1 to 200 g/l of wetting agents, 0 to 200 g/l of antifreeze agents, 0 to 400 g/l of binders, 0 to 200 g/l of colorants (pigments and/or dyes) and solvents, preferably water.
- Preferred FS formulations of the active compounds for the treatment of the buds usually comprise from 0.5 to 80% of active compound, from 0.05 to 5% of wetting agent, from 0.5 to 15% of dispersant, from 0.1 to 5% of thickener, from 0 to 20% of antifreeze agent, from 0 to 2% of antifoam, from 0 to 15% of tackifier or adhesive, from 0 to 75% of filler/vehicle, and from 0.01 to 1 % of preservative.
- Suitable wetting agents and dispersants are in particular the surfactants mentioned above.
- Preferred wetting agents are alkylnaphthalenesulfonat.es, such as diisopropyl- or diisobutylnaphthalenesulfonat.es.
- Preferred dispersants are nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants.
- Suitable nonionic dispersants are in particular ethylene oxide/propylene oxide block copolymers, alkylphenol polyglycol ethers and also tristryrylphenol polyglycol ether, for example polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ether,
- tristerylphenyl polyglycol ether alkylaryl polyether alcohols, alcohol and fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters and methylcellulose.
- Suitable anionic dispersants are in particular alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore arylsulfonate/formaldehyde condensates, for example condensates of sulfonated naphthalene and naphthalene derivatives with
- formaldehyde condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, lignosulfonates, lignosulfite waste liquors, phosphated or sulfated derivatives of methylcellulose and polyacrylic acid salts.
- Suitable for use as antifreeze agents are, in principle, all substances which lower the melting point of water.
- Suitable antifreeze agents include alkanols, such as methanol, ethanol, isopropanol, the butanols, glycol, glycerol, diethylene glycol and the like.
- Suitable thickeners are all substances which can be used for such purposes in agrochemical compositions, for example cellulose derivatives, polyacrylic acid derivatives, xanthane, modified clays and finely divided silica.
- Suitable for use as antifoams are all defoamers customary for formulating
- agrochemically active compounds Particularly suitable are silicone antifoams and magnesium stearate.
- Suitable for use as preservatives are all preservatives which can be employed for such purposes in agrochemical compositions.
- Adhesives/tackifiers may be added to improve the adhesion of the effective
- Suitable adhesives are EO/PO-based block copolymer surfactants, but also polyvinyl alcohols, polyvinyl pyrrolidones,
- polyacrylates polymethacrylates, polybutenes, polyisobutenes, polystyrene, polyethyleneamines, polyethyleneamides, polyethyleneimines (Lupasol®, Polymin®), polyethers and copolymers derived from these polymers.
- Suitable compositions for soil treatment include granules which may be applied in- furrow, as broadcast granules or as impregnated fertilizer granules, and also spray applications which are applied to the soil as a preemergent or postemergent spray.
- Suitable compositions for treating the plants, in particular the overground parts thereof, especially the seedlings (especially the seedlings' leaves), include spray applications, dusts and microgranules, spray applications being preferred.
- Formulations suitable for producing spray solutions for the direct application are: soluble concentrates (SL, LS)
- the treatment may be carried out by mixing the buds with the particular amount desired of active ingredient formulations either as such or after prior dilution with water in an apparatus suitable for this purpose, for example a mixing apparatus for solid or solid/liquid mixing partners, until the composition is distributed uniformly on the buds. If appropriate, this is followed by a drying operation.
- the superabsorbers are generally applied to the growth medium or the field by mixing the growth medium or the soil with them or by applying the desired amount of superabsorber into the holes digged for the bud or the seedling.
- the latter method is preferred for the application of superabsorbers to the field.
- significantly less area is required for reproduction of the sugar cane plants as compared to traditional methods.
- the present method offers a greater flexibility as the buds can be stored and transported to any place.
- the method of the invention also reduces the risk of having non-sprouting sugar cane plants in the filed, which wastes valuable farming land. As the buds/seedlings are protected during the sensitive first growth stages and are only transplanted to the field or exposed to ambient conditions after their rooting system is well developed, the method leads to healthy and vigorous seedlings and adult sugar cane plants growing therefrom.
- step (iii) leads to particularly healthy and vigorous seedlings and adult sugar cane plants growing therefrom and significantly increases the survival rate of the planted buds. Particularly, an increased number of tillers is generally observed, especially if a strobilurin fungicide, especially pyraclostrobin, is used in step (iii).
- a strobilurin fungicide especially pyraclostrobin
- Example 1 On an area of 0.1 hectares where sugar cane plants were growing with a distance between the rows of 1 .5 m, the top part of the 8 months old sugar cane plants was removed by chopping off with a machete in a height of approximately 2 to 2.5 m. The removed top part was discarded. The below, remaining stalks were removed from the field by cutting them off closely above the ground. The stalks were then cut
- the treated buds were then each placed in individual pots filled with humid coconut fibers. 648 bud discs stayed untreated for comparative reasons and were directly placed in individual pots filled with humid coconut fibers.
- the pots were placed in a greenhouse, and seedlings were grown from the planted bud discs at 25 to 35°C and 70 to 80% humidity. While in the greenhouse, the buds/seedlings were watered sufficiently. 30 to 45 days after having been placed in the greenhouse, the surviving seedlings were transferred in an acclimatization area and kept for 15 days. Thereafter they were counted and then transplanted to a field. The results are compiled in the table below.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Soil Sciences (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Cultivation Of Plants (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201280045138.2A CN103826457A (zh) | 2011-09-23 | 2012-09-21 | 栽培甘蔗的方法 |
US14/346,100 US9615503B2 (en) | 2011-09-23 | 2012-09-21 | Method for cultivating sugar cane |
AU2012311471A AU2012311471B2 (en) | 2011-09-23 | 2012-09-21 | Method for cultivating sugar cane |
BR112014006421A BR112014006421A2 (pt) | 2011-09-23 | 2012-09-21 | métodos de cultivo de cana de áçucar |
IN2134CHN2014 IN2014CN02134A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2011-09-23 | 2012-09-21 | |
MX2014003395A MX354962B (es) | 2011-09-23 | 2012-09-21 | Método para cultivar caña de azúcar. |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161538138P | 2011-09-23 | 2011-09-23 | |
EP11182454.6 | 2011-09-23 | ||
EP11182454 | 2011-09-23 | ||
US61/538,138 | 2011-09-23 |
Publications (1)
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WO2013041665A1 true WO2013041665A1 (en) | 2013-03-28 |
Family
ID=47913922
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2012/068625 WO2013041665A1 (en) | 2011-09-23 | 2012-09-21 | Method for cultivating sugar cane |
Country Status (12)
Cited By (4)
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US9615503B2 (en) | 2011-09-23 | 2017-04-11 | Basf Se | Method for cultivating sugar cane |
US10292325B2 (en) | 2013-08-02 | 2019-05-21 | Basf Se | Apparatus for planting and treating seedlings of an agricultural plant |
CN110055191A (zh) * | 2019-04-08 | 2019-07-26 | 浙江大学 | 分离自喷漆废水底泥的拜耶林克氏菌lm-w及其应用 |
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CN114793900A (zh) * | 2022-04-29 | 2022-07-29 | 广西壮族自治区农业科学院 | 一种适宜补种的甘蔗品种的筛选方法及应用 |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3669103A (en) | 1966-05-31 | 1972-06-13 | Dow Chemical Co | Absorbent product containing a hydrocelloidal composition |
US4091569A (en) | 1975-10-09 | 1978-05-30 | Cooperativa Central Dos Produtores De Acucar E Alcool Do Estado De Sao Paulo | Process for the obtaining of sound sugar cane gemmas for the control of the blight of sugar cane stumps left after cutting as well as the gemmas obtained by same process |
US4417992A (en) | 1981-07-30 | 1983-11-29 | Nalco Chemical Company | Dust control |
WO1991014356A1 (en) * | 1990-03-26 | 1991-10-03 | Queensland University Of Technology | Billet planter |
JPH08280244A (ja) * | 1995-04-18 | 1996-10-29 | Dainippon Seito Kk | 甘蔗苗の生産法 |
WO2001025493A1 (fr) | 1999-10-07 | 2001-04-12 | Snf Sa | Utilisation de polymeres superabsorbants pour le traitement des peaux brutes, et procede correspondant et peaux ainsi traitees |
WO2008031870A2 (en) | 2006-09-14 | 2008-03-20 | Basf Se | Pesticide composition |
WO2008095913A2 (en) * | 2007-02-06 | 2008-08-14 | Basf Se | Pesticidal mixtures |
US20080261811A1 (en) * | 2004-12-24 | 2008-10-23 | Bayer Cropscience Ag | Synergistic Mixtures Exhibiting Insecticidal and Fungicidal Action |
EP2005812A1 (en) * | 2007-06-22 | 2008-12-24 | Syngeta Participations AG | A method for growing sugarcane |
WO2011154419A1 (en) * | 2010-06-09 | 2011-12-15 | Basf Se | Method for cultivating sugar cane |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US122936A (en) | 1872-01-23 | Improvement in preserving sugar | ||
FR2753377B1 (fr) | 1996-09-19 | 1999-09-24 | Rhone Merieux | Nouvelle association parasiticide a base de 1-n-phenylpyra- zoles et de lactones macrocycliques endectocides |
BE430419A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1937-10-25 | |||
US2270046A (en) | 1939-11-30 | 1942-01-13 | Honorary Advisory Council Sci | Treatment of plant stem cuttings |
GB926856A (en) | 1960-01-08 | 1963-05-22 | Robert Alexander Spencer Templ | A method of preserving tuber portions for seeding |
US4043077A (en) | 1976-05-10 | 1977-08-23 | Clara Francis Stonehocker | Expandable pot for containing plants and method therefor |
WO1986006576A1 (en) | 1985-05-15 | 1986-11-20 | The Commonwealth Industrial Gases Limited | Method and apparatus for dividing plant materials |
GB8713768D0 (en) | 1987-06-12 | 1987-07-15 | May & Baker Ltd | Compositions of matter |
AU724487B2 (en) | 1996-06-07 | 2000-09-21 | Rhone-Poulenc Rural Australia Pty Ltd | Method of treatment of sugar plant to improve the sugar content |
JPH10324605A (ja) | 1997-05-22 | 1998-12-08 | Nippon Nohyaku Co Ltd | 殺ダニ剤組成物及びその使用方法 |
JP3887879B2 (ja) | 1997-06-06 | 2007-02-28 | ソニーケミカル&インフォメーションデバイス株式会社 | 含フッ素(メタ)アクリル系重合体の製造方法 |
JP3413548B2 (ja) | 1998-10-30 | 2003-06-03 | 株式会社サークル鉄工 | 甘蔗の枝茎苗の移植栽培方法 |
GB9916052D0 (en) | 1999-07-08 | 1999-09-08 | Pfizer Ltd | Anthelmintic compositions |
CN1129358C (zh) | 1999-12-15 | 2003-12-03 | 江苏省新沂中凯农用化工有限公司 | 含有锐劲特的杀虫组合物 |
AU2002228590A1 (en) | 2000-10-10 | 2002-04-29 | John P Harvey | Method of harvesting sugarcane |
US6601527B2 (en) | 2001-03-26 | 2003-08-05 | Herbalscience, Llc | Method of cultivating piper methysticum plants |
JP3774865B2 (ja) | 2002-12-25 | 2006-05-17 | 株式会社サークル鉄工 | 甘蔗の苗用枝茎の栽培生産法 |
DE102004062513A1 (de) | 2004-12-24 | 2006-07-06 | Bayer Cropscience Ag | Insektizide auf Basis von Neonicotinoiden und ausgewählten Strobilurinen |
CN101133738A (zh) | 2006-09-01 | 2008-03-05 | 湖南万家丰科技有限公司 | 一种用于农作物的含氟虫腈杀虫组合物 |
TW200833245A (en) | 2006-10-09 | 2008-08-16 | Syngenta Participations Ag | Pesticidal combinations |
CN101541178A (zh) | 2006-11-17 | 2009-09-23 | 巴斯夫欧洲公司 | 提高植物干生物量的方法 |
CN101621929A (zh) | 2006-11-17 | 2010-01-06 | 巴斯夫欧洲公司 | 提高植物的干生物质的方法 |
CA2690346C (en) | 2007-06-13 | 2013-04-16 | Nippon Paper Industries Co., Ltd. | Method of producing rooted cuttings of tree belonging to the family of pinaceae |
BRPI0814474A8 (pt) | 2007-08-17 | 2018-12-11 | Basf Se | uso de pelo menos um inseticida selecionado a partir de antagonistas de gaba e método de aumento do rendimento de cultura de pelo menos uma variedade de planta |
GB0802849D0 (en) | 2008-02-15 | 2008-03-26 | Syngenta Participations Ag | Process of selecting stem segments |
AU2009214259B8 (en) | 2008-02-15 | 2013-10-31 | Syngenta Participations Ag | Cutting machine |
CH702011B1 (de) | 2009-10-13 | 2014-02-28 | Pack Part Gmbh | Schneidvorrichtung zum Herausschneiden von Stecklingen aus Zuckerrohrstangen. |
WO2011161071A2 (en) | 2010-06-23 | 2011-12-29 | Basf Se | Nematicidal mixtures for use in sugar cane |
MX349859B (es) | 2011-04-15 | 2017-08-16 | Basf Se | Metodo para cultivar caña de azucar. |
WO2013041665A1 (en) | 2011-09-23 | 2013-03-28 | Basf Se | Method for cultivating sugar cane |
WO2013160241A1 (en) | 2012-04-26 | 2013-10-31 | Basf Se | Method and system for extracting buds from a stalk of a graminaceous plant |
WO2013160242A1 (en) | 2012-04-26 | 2013-10-31 | Basf Se | Method and system for extracting buds from a stalk of a graminaceous plant |
GB201210374D0 (en) | 2012-06-12 | 2012-07-25 | New Energy Farms | Plant propagation |
-
2012
- 2012-09-21 WO PCT/EP2012/068625 patent/WO2013041665A1/en active Application Filing
- 2012-09-21 CN CN201280045138.2A patent/CN103826457A/zh active Pending
- 2012-09-21 AU AU2012311471A patent/AU2012311471B2/en not_active Ceased
- 2012-09-21 MX MX2014003395A patent/MX354962B/es active IP Right Grant
- 2012-09-21 US US14/346,100 patent/US9615503B2/en not_active Expired - Fee Related
- 2012-09-21 IN IN2134CHN2014 patent/IN2014CN02134A/en unknown
- 2012-09-21 PE PE2014000406A patent/PE20141523A1/es not_active Application Discontinuation
- 2012-09-21 BR BR112014006421A patent/BR112014006421A2/pt not_active Application Discontinuation
- 2012-09-21 AR ARP120103510A patent/AR087996A1/es unknown
-
2014
- 2014-02-25 CR CR20140090A patent/CR20140090A/es unknown
- 2014-03-04 GT GT201400039A patent/GT201400039A/es unknown
- 2014-03-21 CO CO14061411A patent/CO6920298A2/es unknown
Patent Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3669103A (en) | 1966-05-31 | 1972-06-13 | Dow Chemical Co | Absorbent product containing a hydrocelloidal composition |
US4091569A (en) | 1975-10-09 | 1978-05-30 | Cooperativa Central Dos Produtores De Acucar E Alcool Do Estado De Sao Paulo | Process for the obtaining of sound sugar cane gemmas for the control of the blight of sugar cane stumps left after cutting as well as the gemmas obtained by same process |
US4417992A (en) | 1981-07-30 | 1983-11-29 | Nalco Chemical Company | Dust control |
WO1991014356A1 (en) * | 1990-03-26 | 1991-10-03 | Queensland University Of Technology | Billet planter |
JPH08280244A (ja) * | 1995-04-18 | 1996-10-29 | Dainippon Seito Kk | 甘蔗苗の生産法 |
WO2001025493A1 (fr) | 1999-10-07 | 2001-04-12 | Snf Sa | Utilisation de polymeres superabsorbants pour le traitement des peaux brutes, et procede correspondant et peaux ainsi traitees |
US20080261811A1 (en) * | 2004-12-24 | 2008-10-23 | Bayer Cropscience Ag | Synergistic Mixtures Exhibiting Insecticidal and Fungicidal Action |
WO2008031870A2 (en) | 2006-09-14 | 2008-03-20 | Basf Se | Pesticide composition |
WO2008095913A2 (en) * | 2007-02-06 | 2008-08-14 | Basf Se | Pesticidal mixtures |
EP2005812A1 (en) * | 2007-06-22 | 2008-12-24 | Syngeta Participations AG | A method for growing sugarcane |
WO2009000400A1 (en) | 2007-06-22 | 2008-12-31 | Syngenta Participations Ag | A method for growing sugarcane |
WO2009000401A1 (en) | 2007-06-22 | 2008-12-31 | Syngenta Participations Ag | A method for growing sugarcane |
WO2009000402A1 (en) | 2007-06-22 | 2008-12-31 | Syngenta Participations Ag | A method for growing sugarcane |
WO2009000398A2 (en) | 2007-06-22 | 2008-12-31 | Syngenta Participations Ag | A method for growing sugarcane |
WO2009000399A1 (en) | 2007-06-22 | 2008-12-31 | Syngenta Participations Ag | A method for growing sugarcane |
WO2011154419A1 (en) * | 2010-06-09 | 2011-12-15 | Basf Se | Method for cultivating sugar cane |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9271448B2 (en) | 2010-06-09 | 2016-03-01 | Basf Se | Method for cultivating sugar cane |
US9615503B2 (en) | 2011-09-23 | 2017-04-11 | Basf Se | Method for cultivating sugar cane |
US10292325B2 (en) | 2013-08-02 | 2019-05-21 | Basf Se | Apparatus for planting and treating seedlings of an agricultural plant |
CN110055191A (zh) * | 2019-04-08 | 2019-07-26 | 浙江大学 | 分离自喷漆废水底泥的拜耶林克氏菌lm-w及其应用 |
Also Published As
Publication number | Publication date |
---|---|
CO6920298A2 (es) | 2014-04-10 |
AR087996A1 (es) | 2014-04-30 |
PE20141523A1 (es) | 2014-11-08 |
GT201400039A (es) | 2015-09-23 |
US9615503B2 (en) | 2017-04-11 |
AU2012311471B2 (en) | 2016-06-02 |
BR112014006421A2 (pt) | 2017-04-11 |
IN2014CN02134A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2015-05-29 |
CN103826457A (zh) | 2014-05-28 |
US20140283443A1 (en) | 2014-09-25 |
AU2012311471A1 (en) | 2014-04-10 |
MX354962B (es) | 2018-03-27 |
MX2014003395A (es) | 2014-07-09 |
CR20140090A (es) | 2014-03-21 |
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