The objective of this work was to evaluate the agronomic traits of coffee tree progenies. The experiment was set in Ouro Verde 436-1-4-C26, 516-8-2-C109, 493-1-2-C134, 518-2-10-C408, 514-7-16-C211 and 514-7-16-C208 presented 436-1-4-C26, 516-8-2-C109, 493-1-2-C134, 518-2-10-C408, 514-7-16-C211 e 514-7-16

Meloidogyne enterolobii and M. floridensis are virulent species that can overcome root-knot nematode resistance in economically important crops. Our objectives were to determine the effects of temperature on the infectivity of second-stage juveniles (J2) of these two species and determine differences in duration and thermal-time requirements (degree-days [DD]) to complete their developmental cycle. Florida isolates of M. enterolobii and M. floridensis were compared to M. incognita race 3. Tomato cv. BHN 589 seedlings following inoculation were placed in growth chambers set at constant temperatures of 25°C, and 30°C, and alternating temperatures of 30°C to 25°C (day–night). Root infection by the three nematode species was higher at 30°C than at 25°C, and intermediate at 30°C to 25°C, with 33%, 15%, and 24% infection rates, respectively. There was no difference, however, in the percentages of J2 that infected roots among species at each temperature. Developmental time from infective J2 to reproductive stage for the three species was shorter at 30°C than at 25°C, and 30°C to 25°C. The shortest time and DD to egg production for the three species were 13 days after inoculation (DAI) and 285.7 DD, respectively. During the experimental timeframe of 29 d, a single generation was completed at 30°C for all three species, whereas only M. floridensis completed a generation at 30°C to 25°C. The number of days and accumulated DD for completing the life cycle (from J2 to J2) were 23 d and 506.9 DD for M. enterolobii, and 25 d and 552.3 DD for M. floridensis and M. incognita, respectively. Exposure to lower (25°C) and intermediate temperatures (30°C to 25°C) decreased root penetration and slowed the developmental cycle of M. enterolobii and M. floridensis compared with 30°C.

Foram realizados três experimentos a campo em 1980, no Centro Nacional de Pesquisa de Trigo/EMBRAPA, Passo Fundo, RS, visando conhecer o comportamento dos herbicidas diclofop, dicamba, a associação 2,4 D com dicamba e a mistura diclofop + (2,4 D + dicamba), no controle de azevém (Lolium multiflorum L.) e gorga (Spergula arvensis L.). Ao mesmo tempo foi avaliada a seletividade que estes herbicidas apresentam às culturas de trigo (Triticum aestivum L.), cevada (Hordeum vulgare L.) e centeio (Secale cereale L.). Os resultados da avaliação visual de fitotoxicidade mostra ram que o dicamba causou o maior grau de injúria para as três culturas. Cevada mostrou ser a cultura mais sensível ao dicamba na fase inicial. Trigo, cevada e centeio foram tolerantes ao diclofop. A mistura diclofop + (2,4 D + dicamba) não controlou o azevém nas três culturas. Esta mistura apresentou ainda redução no controle de gorga, nas culturas de cevada e centeio. Dicamba ocasionou redução no rendimento de grãos das culturas, mostrando ser pouco seletivo na dose testada. Centeio sofreu uma redução no rendimento de grãos causada por diclofop, enquanto que a mistura diclofop + (2,4 D + dicamba) foi seletiva para todas as culturas.

New management tools are necessary to reduce the damage caused by the soybean cyst nematode (SCN), Heterodera glycines. Identification of molecules that can stimulate second-stage juveniles (J2) hatching in an environment without food may contribute to that. In in vitro experiments, we evaluate the effect of volatile organic compounds (VOCs) released by soybean (Glycine max), bean (Phaseolus vulgaris), ryegrass (Lolium multiflorum), and alfalfa (Medicago sativa) on H. glycines egg hatching. VOCs released by all plant species significantly (p < 0.05) increased egg hatching. Shortchain molecules released by leaves and roots of soybean and bean increased the hatching up to 71.4%. The analysis of the volatilome done by gas chromatography coupled with mass spectrometry revealed 44 compounds in the plant emissions. Four of them, namely 3-octanol, 1-hexanol, hexanal and linalool were tested individually as hatching inductors. Under concentrations of 200, 600, and 1,000 µg/ml there was no hatching induction of H. glycines J2 by these compounds. On the other hand, in these concentrations, the compounds 3-octanol and 1-hexanol caused hatching reduction with values similar to the commercial nematicide carbofuran (2,3-dihydro-2,2-dimethylbenzofuran-7-yl methyl carbamate). In subsequent tests, the compounds 1-hexanol and 3-octanol showed lethal concentration values required to kill 50% of thenematode population (LC 50 ) of 210 and 228 µg/ml, respectively, in the first experiment and, 230 and 124 µg/mlin the second one. Although we have not identified any molecules acting as hatching factor (HF), here we present a list (44 candidate molecules) that can be explored in future studies to find an efficient HF.

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