LOSS OF MONOTERPENES FROM Tagetes minuta L. FRUITS AT EARLY DECOMPOSITION PROCESS

LAURET CM; ZUNINO MP; DAMBOLENA S; ZYGADLO JA; LóPEZ ML

Otro; SECOND JOINT MEETING OF THE BIOLOGY SOCIETIES FROM ARGENTINA; 2011

Monoterpenes are secondary metabolites with recognized ecophysiological functions as anti-herbivory, allelopathic and modulators of nutrient cycling. No information is available on the pattern of monoterpenes loss at early decomposition process of Tagetes minuta (Asteraceae), a species with presumably important chemoecological activity. We conducted a litterbag study during a short period of time (35 days) in order to detect the loss of monoterpenes from the essential oil stored in the fruits by means of GC studies. The overall decrease of essential oil content was 59% in contrast to a low decrease of biomass (11.4%). Loss of oxygenated monoterpenes from fruit litter was higher (58.8%) than hydrocarbon monoterpenes (54.3%). Major losses of compounds were registered forTagetes minuta (Asteraceae), a species with presumably important chemoecological activity. We conducted a litterbag study during a short period of time (35 days) in order to detect the loss of monoterpenes from the essential oil stored in the fruits by means of GC studies. The overall decrease of essential oil content was 59% in contrast to a low decrease of biomass (11.4%). Loss of oxygenated monoterpenes from fruit litter was higher (58.8%) than hydrocarbon monoterpenes (54.3%). Major losses of compounds were registered for(Asteraceae), a species with presumably important chemoecological activity. We conducted a litterbag study during a short period of time (35 days) in order to detect the loss of monoterpenes from the essential oil stored in the fruits by means of GC studies. The overall decrease of essential oil content was 59% in contrast to a low decrease of biomass (11.4%). Loss of oxygenated monoterpenes from fruit litter was higher (58.8%) than hydrocarbon monoterpenes (54.3%). Major losses of compounds were registered for â-ocimene (60.1%), (E)-ocimenone (62.6%), (Z)-ocimenone (59%), dihydrotagetone (55.1%) and (Z)-tagetone (57.2%). The pattern of loss for each compound adjusted significantly to linear regressions.-ocimene (60.1%), (E)-ocimenone (62.6%), (Z)-ocimenone (59%), dihydrotagetone (55.1%) and (Z)-tagetone (57.2%). The pattern of loss for each compound adjusted significantly to linear regressions.