Abstract: Provided are compositions comprising a collection of overcoated particles wherein each of the overcoated particles comprises a first coating and a second coating. In one embodiment, the first coating comprises water-insoluble material, for example a fatty compound or a waxy material. In another embodiment, the second coating comprises a water-insoluble polymer or water-resistant film, wherein the water-insoluble polymer of the second coating is different than the water-insoluble material of the first coating. Also provided is a slurry comprising water and overcoated powders provided herein. Also provided is a method of contacting plants or plant parts with a composition or slurry provided herein.

Abstract: The present invention relates to compounds formula (I): wherein P is P1, P2, heterocyclyl or heterocyclyl substituted by one to five Z; and wherein A1, A2, A3, A4, G1, R1, R2, R3, R4, R5, R6, R17, R18, R19 and R20 are as defined herein; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (I) and to methods of using the compounds of formula (I) to control insect, acarine, nematode and mollusc pests.

Abstract: A compound of formula (I): wherein A1, A2, A3, A4, A1?, A2?, A3?, A4?, A5?, A6?, G1, R1, R2, R3, R4, R5a and R5b are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I) or compounds of formula (I?), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising compounds of formula (I) or compounds of formula (I?), and to methods of using compounds of formula (I) or compounds of formula (I?) to combat and control insect, acarine, nematode and mollusc pests.

Abstract: The present invention relates to a to a method of controlling the growth of weeds, in particular, large crabgrass and white clover, using a herbicidal composition comprising mesotrione and a triazolinone herbicide such as sulfentrazone or carfentrazone-ethyl. The invention also relates to the use of this composition.

Abstract: The subject invention is based on unexpected more than additive effect of multiple applications of at least one cyclopropene on crop yield as compared to single applications. Provided are methods of increasing yield of a plant comprising contacting the plant with multiple applications of a cyclopropene. In one aspect, the method comprises (a) contacting the plant with a first composition comprising a cyclopropene; and (b) contacting the plant with a second composition comprising a cyclopropene; thereby increasing the yield of the plant in comparison to a plant not contacted with the first composition and/or the second composition. In another aspect, the method comprises contacting the plant with two or more separate applications of a composition comprising at least one cyclopropene thereby increasing the yield of the plant in comparison to a plant not treated or contacted with two or more separate applications of a composition comprising at least one cyclopropene.

Abstract: The present invention relates to compounds of formula (I): wherein A1, A2, A3, A4, G1, L, Y1, Y2, Y3, Y4, R1, R2, R3 and R4 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to intermediates for preparing compounds of formula (I), to compositions comprising them and to methods of using them to combat and control insect, acarine, nematode and mollusc pests.

Abstract: The use of a compound of formula I wherein Y is a single bond, C?O, C?S or S(O)m where m is 0, 1 or 2; the ring is a 6-membered aromatic or is a 5 or 6 membered heteroaromatic ring; Ra, R1, R2, R4 and R8 are specified organic groups; n and p are independently 0-4; or salts or N-oxides thereof or compositions containing them in controlling insects, acarines, nematodes or molluscs. Novel compounds are also provided.

Abstract: The present invention relates, inter alia, to a novel herbicide formulation comprising: (a) an aqueous phase; (b) an HPPD inhibitor in suspension in the aqueous phase; (c) an encapsulated chloroacetamide or an isoxazoline herbicide in suspension in the aqueous phase; (d) glyphosate and/or glufosinate or an agrochemically acceptable salt thereof, in solution in the aqueous phase. The invention further relates to a process for the preparation of an herbicide formulation of the invention and to a process for the control of unwanted vegetation.

Abstract: The present invention relates to processes for the preparation of compounds of formula IB wherein A1, A2, A3, A4, L, Y1, Y2, R1, R2, R3, R4 and R5 are as defined in the claims, comprising reacting a compound of formula (II) wherein Y1, Y2, L, A1, A2, R1, R2, R3, R4 and R5 are as defined for the compound of formula (I); with hydroxylamine in the presence of water, a base and a chiral phase transfer catalyst, which chiral phase transfer catalyst is a quinine derivative. The invention also relates to compounds of formula IB and enantiomerically enriched mixtures comprising compounds of formula IB.

Abstract: The present invention relates to novel processes for the production of compounds of formula wherein Hal and Hal? are independently selected from Cl and F, and R1 is selected from Cl, F and H.

Abstract: Composition for controlling insects and representatives of the order Acarina, which comprises a combination of variable amounts of one or more compounds of the formula in which A is an unsubstituted or, depending on the possibility of substitution on the ring system, mono- to tetrasubstituted, aromatic or non-aromatic monocyclic or bicyclic heterocyclic radical, in which the substituents of A can be chosen from the group consisting of C1-C3alkyl, C1-C3alkoxy, halogen, halo-C1-C3alkyl, cyclopropyl, halocyclopropyl, C2-C3alkenyl, C2-C3alkynyl, halo-C2-C3alkenyl, halo-C2-C3alkynyl, halo-C1-C3alkoxy, C1-C3alkylthio, Halo-C1-C3alkylthio, allyloxy, propargyloxy, allylthio, propargylthio, haloallyloxy, haloallylthio, cyano and nitro; R is hydrogen, C1-C6alkyl, phenyl-C1-C4alkyl, C3-C6cycloalkyl, C2-C6alkenyl or C2-C6alkynyl; and X is N—NO2 or N—CN, in the free form or in salt form, if appropriate tautomers, in the free form or salt form, and one or more of the compounds (I) to (CLXXXIV) mentioned according to

Abstract: A new Chrysanthemum plant named ‘CIFZ0009’ particularly distinguished by the medium sized yellow colored inflorescences, medium sized rounded and mounded plant habit, and a natural season flowering response of mid-October.

Abstract: A new Pelargonium plant named ‘PEQZ0004’ particularly distinguished by the has large semi-double deep red inflorescences with a more blue hue, good garden performance growing well in sun and shade, lateral plant habit, excellent branching and a foliage that resembles in shape the foliage of Pelargonium×hortorum varieties.

Abstract: A new Lobelia plant named ‘LOBZ0004’ particularly distinguished by the large light blue and white bi-color flowers, medium green foliage, and a vigorous well branched, upright and mounded plant habit.

Abstract: A new Pelargonium plant named ‘PEQZ0001’ particularly distinguished by the large mostly semi-double bright red-purple inflorescences, medium green foliage, good garden performance growing well in both sun and shade, with lateral plant habit, excellent branching and zonal like foliage.

Abstract: A new Pelargonium plant named ‘PEQZ0003’ particularly distinguished by the bright red-purple colored inflorescences held above the medium-green foliage, very heat and drought tolerant with continuous color through the most extreme summer heat, and exceptional edema tolerance on a well-branched plant habit.

Abstract: A new Chrysanthemum plant named ‘CIFZ0008’ particularly distinguished by the greyed-purple ray floret color, medium to large sized decorative inflorescences, medium sized round shaped plant habit and a natural season response of late September to early October.

Abstract: A new Chrysanthemum plant named ‘CIFZ0006’ particularly distinguished by the medium sized decorative-type inflorescences with bicolored greyed-red ray floret color, medium to large sized and round plant habit with a natural season flowering response of mid-late September.

Abstract: A new Chrysanthemum plant named ‘CIDZ0046’ particularly distinguished by single/daisy type flower form with large red and yellow bi-colored ray florets, uniform habit with strong stems, medium yellow-green foliage color, and a 7 week blackcloth flowering response time.

Abstract: A new Chrysanthemum plant named ‘CIDZ0045’ particularly distinguished by the large yellow decorative-type inflorescences, strong stems with glossy foliage with an 8 week blackcloth flowering response time.