O desenvolvimento de muitas doenças pós-colheita está intimamente associado ao amadurecimento dos frutos. As condições ambientais podem afetar tanto o desenvolvimento do patógeno quanto a taxa de amadurecimento dos frutos. O objetivo deste trabalho foi determinar as condições de temperatura e duração do período de molhamento mais favoráveis ao desenvolvimento da antracnose em frutos de goiaba. Frutos de goiaba das cultivares Kumagai (polpa branca) e Pedro Sato (polpa vermelha) destacadas foram inoculadas com suspensão de conídios de Colletotrichum gloeosporioides e C. acutatum e incubados sob temperaturas constantes variando entre 10 e 35ºC e molhamento contínuo de 6 e 24 horas. A severidade e incidência da doença foram avaliadas a cada dois dias durante 12 dias. Não houve infecção nas temperaturas de 10 e 35ºC, independentemente do período de molhamento. As condições ótimas para a infecção do fruto foram sob temperatura de 26 e 27ºC, para 'Kumagai' e de 25 e 26ºC, para 'Pedro Sato', com 24 horas de molhamento. De um modo geral, o desenvolvimento da doença na cultivar Kumagai foi mais afetado pela duração do período de molhamento, comparada com a 'Pedro Sato'. A severidade máxima da doença em frutos ocorreu entre 25 e 30ºC, dependendo da espécie de Colletotrichum, para 'Kumagai'. Para 'Pedro Sato' o diâmetro médio das lesões foi maior em frutos armazenados a 20, 25 e 30ºC do que na cultivar Kumagai, dependendo do período de molhamento e espécie. O período de incubação (6 e 7 dias) e o período de latência (8 e 10 dias) foram mínimos à 30ºC. Estas informações geradas nesse trabalho serão úteis tanto para o desenvolvimento de sistemas de aviso fitossanitário quanto para aumentar o tempo de vida de goiabas após a colheita.

The development of a large number of postharvest diseases is closely associated with fruit ripeness. Environmental conditions may affect both the pathogen development and the fruit ripening rate. The aim of this study was to determine the most favorable temperature and wetness duration to the development of anthracnose in guava fruits. Cultivars 'Kumagai' (white pulp) and 'Pedro Sato' (red pulp) were inoculated with a conidial suspension of Colletotrichum gloeosporioides and C. acutatum and incubated at constant temperature ranging from 10 to 35ºC and wetness duration of 6 and 24 hours. Disease severity and incidence were evaluated at every two days during 12 days. No infection occurred at 10 and 35ºC, regardless of the wetness duration. The optimum conditions for fruit infection were 26 and 27ºC for 'Kumagai' and 25 and 26ºC for 'Pedro Sato', adopting 24 hours of wetness. In general, the disease development in 'Kumagai' cultivar was more affected by the wetness period, compared to 'Pedro Sato'. Disease severity for 'Kumagai' fruits was maximal between 25 and 30ºC , depending on the Colletotrichum species. Regarding 'Pedro Sato', the mean diameter of lesions was greater in fruits stored at 20, 25 and 30ºC , compared to 'Kumagai' cultivar, depending on the wetness period and the species. The incubation period (between 6 and 7 days) and the latent period (between 8 and 10 days) were minimal at 30ºC. The data generated in this study will be useful either for the development of a disease warning system or for the increase in the shelf life of guavas in the postharvest.

Brown rot, caused by Monilinia spp. , is one of the most important peach (Prunuspersica (L.) Batsch) diseases and the main cause of postharvest losses. Currently, alternative methods for postharvest disease control, such as the use of volatiles, are under investigation. The objective of this study was to determine the effects of hexanal on the in vitro development of Monilinia fructicola and M. laxa and on monocyclic components of brown rot on peaches. To evaluate the effect on pathogen development in vitro, a single dose of 215 µL of liquid hexanal was placed on glass jars in closed plastic containers (4.3 L) at the moment of fungi transfer, 24 or 48 h after transferring to Petri dishes. After hexanal application, the Petri dishes were kept inside the containers that were closed for 24 h at 20 ºC. Mycelial growth was measured seven days after hexanal removal. For in vivo assays, inoculated fruits were kept in closed plastic containers, and hexanal was applied at the moment of fruit inoculation or 24 hours thereafter. The monocyclic components infection frequency, expressed as brown rot incidence, lesion diameter and lesion sporulation, were assessed daily for seven days. Overall, hexanal was more effective in inhibiting mycelial growth when applied at the moment of pathogen transfer. Hexanal did not prevent pathogen infection, but reduced lesion diameter and completely inhibited spore production on the fruit for both treatments. Hexanal provides a promising alternative for chemical control and can be used in postharvest handling systems.

O mofo-branco, causado por Sclerotinia sclerotiorum, é uma doença importante na cultura do tomateiro. O objetivo do trabalho foi avaliar o efeito de extratos de plantas, resíduos animais e subprodutos industriais no desenvolvimento micelial e na produção de escleródios do fungo "in vitro". Os tratamentos testados foram diferentes concentrações de licor pirolenhoso, óleo de nim, glutamato monossódico, biossólido e composto orgânico [(borra de café (50%) cinza de carvão (10%), resíduo de milho (25%), esterco de aves (12,5%) e farinha de aves (2,5%)], além de duas testemunhas, sem adição de produtos ao meio e com adição do fungicida procimidone. O fungo submetido aos diferentes tratamentos foi incubado à temperatura de 22ºC e luminosidade constante de 260 lux. Foram avaliadas o crescimento micelial, a produção de escleródios e a viabilidade dos mesmos aos 7 e 17 dias após a repicagem do fungo para meio de neon. O composto orgânico a 30 % mostrou-se eficiente na inibição do crescimento micelial e na produção de escleródios. Este tratamento, assim como o óleo de nim a 0,5%, foi analisado com relação à sua influência na microbiota no solo por meio de uma análise de respirometria, que indicou que ambos os tratamentos foram degradados rapidamente, não causando assim malefícios à mesma.

The white mold, caused by Sclerotinia sclerotiorum, is a very important disease in tomato crops. The objective of this work was to study the effect of plant extracts, animal residues and industrial by-products extracts on the fungus in vitro growth. Treatments consisted of different concentrations of pyrolignous oil, neem oil, monosodium glutamate, sewage sludge and organic compost [coffee residue (50%) coal residue (10%), maize residue (25%), poultry waste (12.5%), poultry meal (2.5%)]. Positive control consisted of Petri dishes with PDA medium and negative control treatment consisted of PDA medium with procymidone. Fungus colonies were incubated at 22ºC and light intensity of 260 lux. Variables such as mycelium growth rate, sclerotia production, and viability 7 and 17 days after the transfer of mycelium disc to neon media were assessed. The extract of organic compost at 30% was effective in controlling mycelial growth and sclerotia production. This treatment, as well as neem oil at 0.5% increased soil respiration.