HEAL DSpace

Essential oils of indigenous in Greece six Juniperus taxa: Chemical composition and larvicidal activity against the West Nile virus vector Culex pipiens

Αποθετήριο DSpace/Manakin

Εμφάνιση απλής εγγραφής

dc.contributor.author Vourlioti-Arapi, F en
dc.contributor.author Michaelakis, A en
dc.contributor.author Evergetis, E en
dc.contributor.author Koliopoulos, G en
dc.contributor.author Haroutounian, SA en
dc.date.accessioned 2014-06-06T06:51:46Z
dc.date.available 2014-06-06T06:51:46Z
dc.date.issued 2012 en
dc.identifier.issn 09320113 en
dc.identifier.uri http://dx.doi.org/10.1007/s00436-011-2706-8 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/5688
dc.subject.other alpha muurolene en
dc.subject.other alpha thujene en
dc.subject.other beta elemene en
dc.subject.other beta phellandrene en
dc.subject.other beta thuyone en
dc.subject.other bornyl acetate en
dc.subject.other camphene en
dc.subject.other camphor en
dc.subject.other carveol en
dc.subject.other carvone en
dc.subject.other caryophyllene en
dc.subject.other citronellol en
dc.subject.other copaene en
dc.subject.other delta cadinene en
dc.subject.other diterpene en
dc.subject.other essential oil en
dc.subject.other gamma cadinene en
dc.subject.other germacrene D en
dc.subject.other humulene en
dc.subject.other larvicidal agent en
dc.subject.other limonene en
dc.subject.other linalool en
dc.subject.other myrcene en
dc.subject.other phenol en
dc.subject.other pinene en
dc.subject.other sabinene en
dc.subject.other terpene en
dc.subject.other terpinene en
dc.subject.other unindexed drug en
dc.subject.other article en
dc.subject.other berry en
dc.subject.other bioassay en
dc.subject.other chemical composition en
dc.subject.other concentration (parameters) en
dc.subject.other Culex pipiens en
dc.subject.other gas chromatography en
dc.subject.other Greece en
dc.subject.other insecticidal activity en
dc.subject.other Juniperus en
dc.subject.other Juniperus drupacea en
dc.subject.other Juniperus foetidissima en
dc.subject.other Juniperus oxycedrus en
dc.subject.other juniperus phoenicea en
dc.subject.other larva en
dc.subject.other mass fragmentography en
dc.subject.other nonhuman en
dc.subject.other phytochemistry en
dc.subject.other priority journal en
dc.subject.other wood en
dc.subject.other Animals en
dc.subject.other Biological Assay en
dc.subject.other Culex en
dc.subject.other Female en
dc.subject.other Gas Chromatography-Mass Spectrometry en
dc.subject.other Greece en
dc.subject.other Insecticides en
dc.subject.other Juniperus en
dc.subject.other Larva en
dc.subject.other Oils, Volatile en
dc.subject.other Survival Analysis en
dc.subject.other Culex pipiens en
dc.subject.other Juniperus en
dc.subject.other Juniperus drupacea en
dc.subject.other Juniperus phoenicea en
dc.subject.other West Nile virus en
dc.title Essential oils of indigenous in Greece six Juniperus taxa: Chemical composition and larvicidal activity against the West Nile virus vector Culex pipiens en
heal.type journalArticle en
heal.identifier.primary 10.1007/s00436-011-2706-8 en
heal.publicationDate 2012 en
heal.abstract The chemical composition of 14 essential oils (EOs), obtained from various parts (leaves, fruits, wood) of the six indigenous in Greece Juniperus family taxa, was determined by GC and GC/MS analysis. The insecticidal properties of these EOs were evaluated against Culex pipiens L. larvae of 3rd and early 4th instars, in order to delineate the relationship between the phytochemical content of the EOs and their larvicidal activities. The analytical data indicated that the EOs mainly consisted of monoterpenes, mostly cyclic and only occasionally aliphatic, and to a lesser percent, of diterpenes. The larvicidal bioassays against C. pipiens larvae revealed that the most active EO was derived from the wood of Juniperus drupacea and contains mainly non-oxygenated monoterpenes and a significant amount of diterpenes, displaying the highest chemodiversity. Its initial LC 50 value was 26.47 mg L -1. On the contrary, the EO isolated from J. phoenicea berries, which consisted of monoterpenes (non-oxygenated, cyclic), was the less active displaying an LC 50 value of 96.69 mg L -1. In respect to the contained phytochemicals, myrcene was assayed as the most toxic, displaying an LC 50 value of 33.83 mg L -1, while the four isomers of pinene abundant in all EOs were less active exhibiting LC 50 values ranging from 70.40 to 94.88 mg L -1. Results herein reveal that the EOs isolated from the studied Juniperus family taxa represent an inexpensive source of natural mosquito control mixtures. © Springer-Verlag 2012. en
heal.journalName Parasitology Research en
dc.identifier.issue 5 en
dc.identifier.volume 110 en
dc.identifier.doi 10.1007/s00436-011-2706-8 en
dc.identifier.spage 1829 en
dc.identifier.epage 1839 en


Αρχεία σε αυτό το τεκμήριο

Αρχεία Μέγεθος Μορφότυπο Προβολή

Δεν υπάρχουν αρχεία που σχετίζονται με αυτό το τεκμήριο.

Αυτό το τεκμήριο εμφανίζεται στην ακόλουθη συλλογή(ές)

Εμφάνιση απλής εγγραφής

Αναζήτηση DSpace


Σύνθετη Αναζήτηση

Αναζήτηση

Ο Λογαριασμός μου

Στατιστικές