Efficacy of lufenuron as chemosterilant against Ceratitis capitata in field trials.

Two field trials in citrus orchards in Turis (Valencia, Spain) and Denia (Alicante, Spain) were performed in order to test the sterilant effect of the insect growth regulator lufenuron against wild medfly Ceratitis capitata (Wiedemann) populations. Two application methods for lufenuron were tested: spraying, in spots, an emulsion of lufenuron in a protein bait, and hanging delta traps that contained a proteinaceous gel with lufenuron (solid bait). The sterilant effect was measured as medfly population reduction, reduction of fruit damage in treated fields, and the number of eggs hatching in punctured fruits. In order to assess the efficacy of lufenuron treatments, we recorded results obtained from two different zones in both trial fields: an outer zone, close to untreated fields, and an inner zone, in the centre of lufenuron treated fields. We observed a minimum sterilant effect in the outer zone and a maximum sterilant effect in the inner one. The maximum sterilant effect was in the inner zone, where a reduction of medfly population of 80.4% in the sprayed field and a reduction of 77.6% in the solid bait field was observed. In addition, the greater the distance from the untreated zones of the treated orchard (inwards), the lower the fruit damage and medfly population level. In this inner zone, fruit punctured by medfly developed significantly fewer larvae (38.8%) than punctured fruits from the outer zone (68.6%). In addition, we recorded the decline in the activity of the lufenuron treatments with time. Lufenuron activity persisted in field for at least 2 weeks with spray applications, and for 3 months with bait gels.

Fungicidal potential of methoxylated flavones from citrus for in vitro control of Colletotrichum gloeosporioides, causal agent of anthracnose disease in tropical fruits.

Four polymethoxylated flavones (3,5,6,7,3',4'-hexamethoxyflavone, 3,5,6,7,8,3',4'-heptamethoxyflavone, 5,6,7,8,4'-pentamethoxyflavone and 5,6,7,8,3',4'-hexamethoxyflavone) were isolated and characterized from cold-pressed orange oil. Their antifungal activities were evaluated against Colletotrichum gloeosporioides (Penz) Penz & Sacc, a major plant pathogen of fruits that causes significant damage to crops in tropical, sub-tropical and temperate regions. Methoxylated flavones were effective in inhibiting mycelial growth of the fungus. As flavone concentration increased, mycelial growth decreased. 5,6,7,8,3',4'-Hexamethoxyflavone completely inhibited the growth of Cgloeosporioides at a concentration of 100 microg ml(-1).

Insecticidal activity of penitrems, including penitrem G, a new member of the family isolated from Penicillium crustosum.

Penitrem G (7), a new indole-diterpenoid compound, has been isolated together with the already known mycotoxins penitrems A-D (1-4) and F (6) from the mycelium of Penicillium crustosum Thom. The structure of penitrem G was established on the basis of spectroscopic data. In addition, paspaline (8), another indole-diterpenoid mycotoxin that has not been previously described in this fungus, was also isolated. These compounds were tested for insecticidal activity against the hemipteran Oncopeltus fasciatus Dallas and the dipteran Ceratitis capitata Wiedemann. Penitrems A-D and F showed convulsive and insecticidal activities against both insect species. In addition, important reductions in the fecundity and fertility of the surviving C. capitata females were observed. In contrast, penitrem G and paspaline did not show any kind of activity. Mortality data and sublethal effects of the treatments have allowed preliminary structure-activity relationships to be proposed.

Globularia alypum L. extracts reduced histamine and serotonin contraction in vitro.

The present study analyses in in vitro models the pharmacological activity of methanol and dichloromethane extracts (1, 10 and 100 microg/mL) obtained from the leaves and stems of Globularia alypum L. Preincubation of the guinea-pig ileum and rat uterus with both extracts produced a dose dependent abolition of the contractile effects of histamine and serotonin, respectively. At the same doses, neither methanol nor dichloromethane extract reduced the contractile effects of acetylcholine on rat duodenum or noradrenaline on rat vas deferens.

Pharmacological properties of the methanol extract from Mentha suaveolens Ehrh.

The present study analyses the pharmacological activity in in vivo and in vitro models of the methanol extract obtained from the leaves and steams of Menta suaveolens Ehrh. This extract lacked toxicity, but exhibited a central nervous system depressant action; an analgesic effect in models of chemical and mechanical stimulation suggesting the induction of a peripheral analgesic response. The extract also exhibited an antiinflammatory action inhibiting the rat paw oedema induced by carrageenin. Moreover, the in vitro studies showed a significant diminution in the contractile effects induced by histamine, serotonin and acetylcholine.