Criteris de collita per poma Gala i Golden: l’opinió del consumidor

Estudis de mercat indiquen que la millora de la qualitat de les pomes és un dels factors que més influència poden tenir per estimular la demana dels consumidors (Harker, 2001; Harker et al, 2003). En aquest sentit, millorar la qualitat del producte implica oferir al consumidor el producte que ell desitja d’acord amb les seves preferències gustatives. No obstant, és obvi que no existeix un producte que pugui satisfer al 100% de la població, sinó grups de consumidors amb unes preferències gustatives diferenciades. Identificar els grups de consumidors que responen positivament a uns atributs sensorials específics, permet dirigir el producte d’unes característiques qualitatives determinades al segment de mercat adequat per satisfer les expectatives del consumidor. Sabent que les característiques organolèptiques dels fruits en el moment del seu consum depenen en gran part de l’estat de maduresa del fruit en el moment de collita, es va plantejar un estudi amb la finalitat de definir un criteri racional de collita per a pomes del grup ‘Gala’ i ‘Golden’ en base a les preferències gustatives del consumidor1. Per a cada varietat, es van plantejar 2 objectius: 1. Identificar i quantificar els segments de població amb preferències gustatives diferenciades. 2. Determinar els paràmetres de qualitat que cal tenir en compte i els seus valors òptims a collita per satisfer el consumidor de poma ‘Gala’ i ‘Golden’ després d’un període de llarga conservació.

Bases boquímicas de resistencia a Penicillium expansum en manzana "golden delicious"

La producción frutícola española es muy importante y los problemas relacionados con su conservación, sobre todo desde la entrada de España en la UE, tienen un interés peculiar con el objetivo de mejorar la calidad y disminuir el uso de los productos susceptibles de perjudicar la salud humana. Para conseguir avances importantes en el aspecto tecnológico se precisa una profundización en los fenómenos bioquímicos que determinan las capacidades de conservación del fruto. Dentro de la complejidad de esta temática, este proyecto pretende determinar los factores bioquímicos involucrados en el control de podredumbres en la fruta y más específicamente los factores endógenos que determinan la resistencia del fruto a este tipo de daños. El objetivo general de este proyecto era de definir los mecanismos bioquímicos involucrados en la resistencia de la manzana ‘Golden Delicious’ contra la acción de un patógeno: Penicillium expansum. Para lograr este objetivo se plantearon las diferentes tareas: Tarea 1 (T1): determinación de madurez y del estado fisiológico a la cosecha Tarea 2 (T2): determinación de las capacidades de resistencia endógenas iniciales e influencia del estado de madurez a la cosecha Tarea 3 (T3): respuesta inicial a una inoculación artificial: cambios bioquímicos y sensibilidad al patógeno Tarea 4 (T4): comportamiento después de conservación: respuesta a una inoculación (cambios bioquímicos y sensibilidad al patógeno) y sensibilidad natural durante la conservación Tarea 5 (T5): determinación de un esquema explicativo y caracterización de los factores bioquímicos determinantes Tarea 6 (T6): elaboración de un test de predicción.

The effects of feeding Karlodinium veneficum (PLY # 103; Gymnodinium veneficum Ballantine) to the blue mussel Mytilus edulis

The effects of exposure to the type species for Karlodinium veneficum (PLY # 103) on immune function and histopathology in the blue mussel Mytilus edulis were investigated. Mussels from Whitsand Bay, Cornwall (UK) were exposed to K. veneficum (PLY # 103) for 3 and 6 days. Assays for immune function included total and differential cells counts, phagocytosis and release of extra cellular reactive oxygen species. Histology was carried out on digestive gland and mantle tissues. The toxin cell quota for K. veneficum (PLY #103) was measured by liquid chromatography-mass spectrometry detecting two separable toxins KvTx1 (11.6 ± 5.4 ng/ml) and KvTx2 (47.7 ± 4.2 ng/ml). There were significant effects of K. veneficum exposure with increasing phagocytosis and release of reactive oxygen species following 6 days exposure. There were no significant effects on total cell counts. However, differential cell counts did show significant effects after 3 days exposure to the toxic alga. All mussels produced faeces but not pseudofaeces indicating that algae were not rejected prior to ingestion. Digestive glands showed ingestion of the algae and hemocyte infiltration after 3 days of exposure, whereas mantle tissue did not show differences between treatments. As the effects of K. veneficum were not observed in the mantle tissue it can be hypothesized that the algal concentration was not high enough, or exposure long enough, to affect all the tissues. Despite being in culture for more than 50 years the original K. veneficum isolate obtained by Mary Parke still showed toxic effects on mussels.

Pathology and immune response of the blue mussel (Mytilus edulis L.) after an exposure to the harmful dinoflagellate Prorocentrum minimum

The harmful dinoflagellate Prorocentrum minimum has different effects upon various species of grazing bivalves, and these effects also vary with life-history stage. Possible effects of this dinoflagellate upon mussels have not been reported; therefore, experiments exposing adult blue mussels, Mytilus edulis, to P. minimum were conducted. Mussels were exposed to cultures of toxic P. minimum or benign Rhodomonas sp. in glass aquaria. After a short period of acclimation, samples were collected on day 0 (before the exposure) and after 3, 6, and 9 days of continuous-exposure experiment. Hemolymph was extracted for flow-cytometric analyses of hemocyte, immune-response functions, and soft tissues were excised for histopathology. Mussels responded to P. minimum exposure with diapedesis of hemocytes into the intestine, presumably to isolate P. minimum cells within the gut, thereby minimizing damage to other tissues. This immune response appeared to have been sustained throughout the 9-day exposure period, as circulating hemocytes retained hematological and functional properties. Bacteria proliferated in the intestines of the P. minimum-exposed mussels. Hemocytes within the intestine appeared to be either overwhelmed by the large number of bacteria or fully occupied in the encapsulating response to P. minimum cells; when hemocytes reached the intestine lumina, they underwent apoptosis and bacterial degradation. This experiment demonstrated that M. edulis is affected by ingestion of toxic P. minimum; however, the specific responses observed in the blue mussel differed from those reported for other bivalve species. This finding highlights the need to study effects of HABs on different bivalve species, rather than inferring that results from one species reflect the exposure responses of all bivalves.

Experimental exposure of the blue mussel (Mytilus edulis, L.) to the toxic dinoflagellate Alexandrium fundyense: Histopathology, immune responses, and recovery

Mussels (Mytilus edulis) were exposed to cultures of the toxic dinoflagellate Alexandrium fundyense or the non-toxic alga Rhodomonas sp. to evaluate the effects of the harmful alga on the mussels and to study recovery after discontinuation of the A. fundyense exposure. Mussels were exposed for 9 days to the different algae and then all were fed Rhodomonas sp. for 6 more days. Samples of hemolymph for hemocyte analyses and tissues for histology were collected before the exposure and periodically during exposure and recovery periods. Mussels filtered and ingested both microalgal cultures, producing fecal pellets containing degraded, partially degraded, and intact cells of both algae. Mussels exposed to A. fundyense had an inflammatory response consisting of degranulation and diapedesis of hemocytes into the alimentary canal and, as the exposure continued, hemocyte migration into the connective tissue between the gonadal follicles. Evidence of lipid peroxidation, similar to the detoxification pathway described for various xenobiotics, was found; insoluble lipofuchsin granules formed (ceroidosis), and hemocytes carried the granules to the alimentary canal, thus eliminating putative dinoflagellate toxins in feces. As the number of circulating hemocytes in A. fundyense-exposed mussels became depleted, mussels were immunocompromised, and pathological changes followed, i.e., increased prevalences of ceroidosis and trematodes after 9 days of exposure. Moreover, the total number of pathological changes increased from the beginning of the exposure until the last day (day 9). After 6 days of the exposure, mussels in one of the three tanks exposed to A. fundyense mass spawned; these mussels showed more severe effects of the toxic algae than non-spawning mussels exposed to A. fundyense. No significant differences were found between the two treatments during the recovery period, indicating rapid homeostatic processes in tissues and circulating hemocytes.

DNA's golden jubilee.

Review of : 50 Years of DNA Foreword by Phil Campbell, edited by Julie Clayton and Carina Dennis Palgrave Macmillan

Persistence of experimental Rocio virus infection in the golden hamster (Mesocricetus auratus)

Rocio virus (ROCV) is an encephalitic flavivirus endemic to Brazil. Experimental flavivirus infections have previously demonstrated a persistent infection and, in this study, we investigated the persistence of ROCV infection in golden hamsters (Mesocricetus auratus). The hamsters were infected intraperitoneally with 9.8 LD50/0.02 mL of ROCV and later anaesthetised and sacrificed at various time points over a 120-day period to collect of blood, urine and organ samples. The viral titres were quantified by real-time-polymerase chain reaction (qRT-PCR). The specimens were used to infect Vero cells and ROCV antigens in the cells were detected by immunefluorescence assay. The levels of antibodies were determined by the haemagglutination inhibition technique. A histopathological examination was performed on the tissues by staining with haematoxylin-eosin and detecting viral antigens by immunohistochemistry (IHC). ROCV induced a strong immune response and was pathogenic in hamsters through neuroinvasion. ROCV was recovered from Vero cells exposed to samples from the viscera, brain, blood, serum and urine and was detected by qRT-PCR in the brain, liver and blood for three months after infection. ROCV induced histopathological changes and the expression of viral antigens, which were detected by IHC in the liver, kidney, lung and brain up to four months after infection. These findings show that ROCV is pathogenic to golden hamsters and has the capacity to cause persistent infection in animals after intraperitoneal infection.

Higgin’s-eye Pearly Mussel Lampsilis higginsi, 2011

Data sheet produced by the Iowa Department of Natural Resources is about different times of animals, insects, snakes, birds, fish, butterflies, etc. that can be found in Iowa.

Presence of the alien chinese pond mussel Anodonta woodiana (Lea, 1834) (Bivalvia, Unionidae) in the Iberian Peninsula

Nota sobre les conseqüències de la invasió del mol·lusc d'aigua dolça, Anodonta woodiana, a la Península Ibèrica

Potassium permanganate effects in postharvest conservation of the papaya cultivar Sunrise Golden

The objective of this work was to evaluate the effects of KMnO4 on the extension of postharvest life of 'Sunrise Golden' papaya, stored under modified atmosphere and refrigeration. Fruit with up to 10% yellow peel were harvested in a commercial orchard in Linhares, state of Espírito Santo, Brazil. Sets of three fruit (unit mass of 289.9±18.5 g) were wrapped in low-density polyethylene films (28 ¼m thick) containing sachets of KMnO4 at 0, 0.5, 1, 1.5, and 2 g per bag. The bags were sealed and stored at 10.4±0.9°C and 90±5% relative humidity for 25 days. After this period, the fruit were removed from the bags and maintained at 21±0.8°C and 90±5% relative humidity until complete ripening. Four days after bag sealing, CO2 concentration stabilized in all treatments, and was higher in bags without KMnO4. In all treatments, fruit reached the climacteric respiratory peak on the third day after bag removal, coinciding with peel color index of 3.5. Increasing the KMnO4 dose reduced the losses in fruit fresh matter, consistency and pulp electrolyte leakage. Potassium permanganate was effective in maintaining the fruit at the pre-climacteric stage during the 25-day storage, and did not interfere with normal ripening after bag removal.

EFEITO DO CARBARYL SOBRE O 'RUSSETING' DA MAÇÃ (MALUS DOMESTICA BORKH.), CULTIVARES 'GALA', 'FUJI' E 'GOLDEN DELICIOUS'

O "russeting" da maçã caracteriza-se por uma camada de cortiça formada entre as células da epiderme e que dá um aspecto de rugosidade à superfície do fruto, depreciando-o para a comercialização. O raleio de frutos é uma prática cultural bastante difundida entre os produtores de maçã. Pode ser efetuada manualmente, quimicamente ou pela associação de ambos. Dentre os produtos mais usados para raleio químico, estão o ácido naftaleno acético (ANA) e o carbaryl, um inseticida carbamato, conhecido comercialmente como Sevinâ. Há duas formulações de carbaryl no mercado brasileiro, mas não existem dados de pesquisa suficientes que permitam escolher a formulação mais adequada. Há citações de que o carbaryl pode causar "russeting" em maçãs. O objetivo deste trabalho foi testar as duas formulações de carbaryl existentes no mercado, quanto ao seu efeito sobre o "russeting" nas maçãs. Os experimentos foram conduzidos em Fraiburgo e em Caçador, Santa Catarina, Brasil. Foram avaliadas duas concentrações, 500 ppm e 1.500 ppm de carbaryl. Foram testadas duas formulações, uma em pó-molhável com 85% de i.a. e outra em suspensão concentrada com 48% de i.a. Como a incidência de "russeting" varia entre cultivares, testou-se em 'Gala', 'Fuji' e 'Golden Delicious', que são as três mais importantes no mercado brasileiro. Os resultados mostraram que: 1) A ocorrência de "russeting" para as três cultivares foi maior em Fraiburgo do que em Caçador; 2) O carbaryl, na formulação solução concentrada, causou mais "russeting" em 'Golden Delicious', em Caçador, indicando que o seu uso deve ser evitado para essa cultivar, dando-se preferência à formulação pó-molhável; 3)Tanto a formulação quanto a concentração de carbaryl não afetaram a incidência de "russeting" nas cultivares 'Gala' e 'Fuji' nos dois locais.

Caracterização do estádio de maturação do papaia 'Golden' em função da cor

A mudança de cor da casca é uma das variáveis físicas mais utilizadas para avaliar os estádios de maturação de frutas. O mamão apresenta a característica de mudança gradual da cor da casca de verde para amarela. Essa mudança gradual e de maneira desuniforme dificulta a utilização de escalas nominais que estão sujeitas à interpretação e fadiga do observador. Neste trabalho, foram realizadas leituras no papaia 'Golden' tipo exportação. Neste trabalho, foram realizadas leituras dos parâmetros L, a, b e refletância da casca em 100 frutos para os estádios de maturação 2; 3; 4 e 5. Os resultados obtidos indicaram que os parâmetros de Hunter a e b e refletância na casca na região do amarelo e alaranjado são promissoras como medidas físicas objetivas para avaliar os estádios de maturação do papaia 'Golden'.