2006
DOI: 10.1515/bot.2006.006
|View full text |Cite
|
Sign up to set email alerts
|

Volatile compounds from some Black Sea red algae and their chemotaxonomic application

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

3
19
0
4

Year Published

2010
2010
2022
2022

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 41 publications
(26 citation statements)
references
References 31 publications
3
19
0
4
Order By: Relevance
“…In Palisada perforata (Bory) K.W. Nam, previous called as Laurencia papillosa, the SPF-1 and SPF-2 production was seen in our study, which is consistent with other terpenes already indentified by Kamenarska et al (2006).…”
Section: Resultssupporting
confidence: 91%
See 1 more Smart Citation
“…In Palisada perforata (Bory) K.W. Nam, previous called as Laurencia papillosa, the SPF-1 and SPF-2 production was seen in our study, which is consistent with other terpenes already indentified by Kamenarska et al (2006).…”
Section: Resultssupporting
confidence: 91%
“…In Palisada perforata (Bory) K.W. Nam, previous called as Laurencia papillosa, the SPF-1 and SPF-2 production was seen in our study, which is consistent with other terpenes already indentified by Kamenarska et al (2006).As can be seen in Table 3, both compounds SPF-1 and SPF-2 were observed in different seaweed species, in amounts ranging from 1.12±0.37 to 53.25± 0.21%.Regarding the proportion of the fragments analyzed, most of the species that have the sesquiterpenes SPF-1 and SPF-2 in his composition showed higher percentage of the m/z 86 (in a proportion of 2:1), indicating that the compound SPF-2 is twofold higher. On the other hand, the proportion found between m/z 86 and m/z 98 was 1.5:1 for Palisada perforata (Bory) K.W.…”
supporting
confidence: 91%
“…Studies of the volatiles in algae were conducted by extraction and pre-concentration by conventional methods: liquid-liquid extraction [9], distillation [6,[10][11][12][13][14] and pre-evaporation [15]. These methods present several disadvantages as use of expensive and hazardous organic solvents, lose analytes during extraction and high time consuming.…”
Section: Introductionmentioning
confidence: 99%
“…[3] β-Ionone is an aroma compound that comes from the degradation of β-carotene via a 9,10-cleavage of the double bond by a carotenoid cleavage dioxygenase (Figure 1). [4,5] This norisoprenoid has been already detected in natural products such as algae, [6][7][8] cyanobacteria, [6,9] fruits, [5,10] wine, [11] fl owers [5] and, more recently, marine salt [1] . Norisoprenoids usually show low odour threshold values; β-ionone has an odour threshold in water of 30 ng/l.…”
Section: Introductionmentioning
confidence: 99%
“…[1] According to the chromatographic profi les previously obtained from marine salt, [1] it is expected that β-ionone exists at trace levels; thus, an extraction/enrichment technique is required. HS-SPME, [1,10] SBSE (stir bar sorptive extraction), [15] purge and trap, [16] liquid-liquid and solid-liquid extraction [7,8,11] have been reported for the extraction of β-ionone from several types of matrices. Based on our previous experience on analysis of marine salt, and considering that SPME is rapid, easy to use, solvent-free and sensitive, as evidenced by studies from a large number of products, [17] it was selected as the best option for this study.…”
Section: Introductionmentioning
confidence: 99%