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Article

Mosquito Larvicidal Activity, Antimicrobial Activity, and Chemical Compositions of Essential Oils from Four Species of Myrtaceae from Central Vietnam

by
Nguyen Thi Giang An
1,
Le Thi Huong
1,
Prabodh Satyal
2,
Thieu Anh Tai
3,
Do Ngoc Dai
4,5,
Nguyen Huy Hung
6,*,
Nguyen Thi Bich Ngoc
7 and
William N. Setzer
2,8,*
1
School of Natural Science Education, Vinh University, 182 Le Duan, Vinh City 43000, Nghe An Province, Vietnam
2
Aromatic Plant Research Center, 230 N 1200 E, Suite 102, Lehi, UT 84043, USA
3
Department of Pharmacy, Duy Tan University, 03 Quang Trung, Da Nang 50000, Vietnam
4
Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18-Hoang Quoc Viet, Cau Giay, Hanoi 10072, Vietnam
5
Faculty of Agriculture, Forestry and Fishery, Nghe An College of Economics, 51-Ly Tu Trong, Vinh City 4300, Nghe An Province, Vietnam
6
Center for Advanced Chemistry, Institute of Research and Development, Duy Tan University, 03 Quang Trung, Da Nang 550000, Vietnam
7
Pedagogical Institute of Science, Vinh University, 182 Le Duan, Vinh City 43000, Vietnam
8
Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA
*
Authors to whom correspondence should be addressed.
Plants 2020, 9(4), 544; https://0-doi-org.brum.beds.ac.uk/10.3390/plants9040544
Submission received: 24 March 2020 / Revised: 5 April 2020 / Accepted: 19 April 2020 / Published: 22 April 2020
(This article belongs to the Special Issue 2019 Feature Papers by Plants’ Editorial Board Members)
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Abstract

:
Mosquitoes are important vectors of several diseases, and control of these insects is imperative for human health. Insecticides have proven useful in controlling mosquito populations, but insecticide resistance and environmental concerns are increasing. Additionally, emerging and re-emerging microbial infections are problematic. Essential oils have been shown to be promising mosquito larvicidal agents as well as antimicrobial agents. In this work, the essential oils from four species of Myrtaceae (Baeckea frutescens, Callistemon citrinus, Melaleuca leucadendra, and Syzygium nervosum) growing wild in central Vietnam have been obtained by hydrodistillation and analyzed by gas chromatographic techniques. The essential oils have been screened for mosquito larvicidal activity against Aedes aegypti, Aedes albopictus, and Culex quinquefasciatus, and for antimicrobial activity against Enterococcus faecalis, Staphylococcus aureus, and Candida albicans. Callistemon citrinus fruit essential oil, rich in α-pinene (35.1%), 1,8-cineole (32.4%), limonene (8.2%), and α-terpineol (5.8%) showed good larvicidal activity with 24-h LC50 = 17.3 μg/mL against both Ae. aegypti and Cx. quinquefasciatus, and good antibacterial activity against E. faecalis (minimum inhibitory concentration (MIC) = 16 μg/mL) The 48-h larvicidal activities of M. leucadendra leaf essential oil, rich in α-eudesmol (17.6%), guaiol (10.9%), linalool (5.1%), (E)-caryophyllene (7.0%), and bulnesol (3.6%) were particularly notable, with LC50 of 1.4 and 1.8 μg/mL on Ae. aegypti and Cx. quinquefasciatus. Similarly, M. leucadendra bark essential oil, with α-eudesmol (24.1%) and guaiol (11.3%), showed good antibacterial activity against. E. faecalis. Both B. frutescens and C. citrinus leaf essential oils demonstrated anti-Candida activities with MIC values of 16 μg/mL. The results of this investigation suggest that essential oils derived from the Myrtaceae may serve as “green” alternatives for the control of mosquitoes and/or complementary antimicrobial agents.

Graphical Abstract

1. Introduction

Mosquitoes are important vectors of diseases and kill more humans than any other animal. Aedes aegypti (L.) and Ae. albopictus (Skuse) (Diptera: Culicidae) are vectors of the yellow fever, dengue, Zika, and chikungunya viruses [1,2,3]; Culex quinquefasciatus (Say) is the primary vector of the Saint Louis encephalitis and West Nile viruses, as well as the filarial nematode Wuchereria bancrofti, and may also be a vector of the Zika virus [4].
Microbial infections continue to be a problem, for humans [5], as well as for livestock and other agriculture settings [6,7,8]. Compounding this problem are newly emerging pathogenic microorganisms, in addition to re-emerging multidrug-resistant pathogens [9,10].
The Myrtaceae is comprised of 131 genera and around 5500 species, all of which are woody trees or shrubs and contain essential oils [11]. Several members of the family are commercially important for their medicinal essential oils, such as clove (Syzygium aromaticum (L.) Merr. & L.M. Perry), tea tree (Melaleuca alternifolia Cheel), allspice (Pimenta dioica (L.) Merr.), and Eucalyptus. In this work, we present the essential oil compositions of four species of Myrtaceae growing wild in central Vietnam, their larvicidal activities against Ae. aegypti, Ae. albopictus, and Cx. quinquefasciatus, and their antimicrobial activities against Enterococcus faecalis, Staphylococcus aureus, and Candida albicans.
Baeckea frutescens L. (syn. Baeckea chinensis Gaertn., Baeckea cochinchinensis Blume, Baeckea sumatrana Blume) is a shrub or small tree that ranges throughout southeastern China (including the provinces of Fujian, Guangdong, Guangxi, Hainan, Jaingxi, and Zhejiang), Burma, Cambodia, India, the Philippines, Thailand, and Vietnam [12].
Callistemon citrinus (Curtis) Skeels (syn. Melaleuca citrina (Curtis) Dum. Cours., Callistemon lanceolatus DC., Callistemon lanceolatus Sweet, Metrosideros citrinus Curtis, Metrosideros lanceolata Sm.) is a shrub or small tree, native to Australia, but has been introduced to tropical and subtropical regions worldwide [13].
Melaleuca leucadendra (L.) L. (syn. Melaleuca viridiflora C.F. Gaertn., Myrtus leucadendra L.) is a tree growing as large as 40 m in height, native to tropical Australia (Queensland, Northern Territory, and Western Australia, New Guinea, and islands of eastern Indonesia [14]. The tree has been introduced to other tropical areas [12], including Vietnam, where it is grown for use as poles and construction materials [14].
Syzygium nervosum DC. (syn. Cleistocalyx operculatus (Roxb.) Merr. & L.M.Perry, Eugenia operculata Roxb.) is a medium-sized tree native to the Asian tropics, from southern China (Guangdong, Guangxi, Hainan, Xizang Zizhiqu, and Yunnan provinces), India, Burma, Sri Lanka, Thailand, and Vietnam [12], and south into eastern Australia [15].
Photographs of the plants presented in this work are shown in Figure 1.

2. Results and Discussion

2.1. Chemical Compositions

The essential oil from the fresh leaves of Baeckea frutescens was obtained in a yield of 2.23%. The leaf essential oil composition of B. frutescens is presented in Table 1. A total of 88 compounds were identified accounting for 100% of the essential oil composition, with monoterpene hydrocarbons (55.6%) predominating. The major components were α-pinene (11.1%), β-pinene (19.0%), p-cymene (8.9%), 1,8-cineole (10.1%), γ-terpinene (11.7%), (E)-caryophyllene (7.1%), and α-humulene (9.9%). Leaf essential oil compositions have previously been reported from Vietnam [16,17,18], China [19], and from Malaysia [20]. The compositions of these essential oils have shown remarkable chemical variation. Nevertheless, the composition of B. frutescens in this present study is very similar to that found in a sample collected from Đồng Hới, Quảng Bình Province [16], and sample 2 (from Sóc Sơn District, Hanoi) reported by Tam and co-workers [17].
The leaf and fruit essential oils of Callistemon citrinus were obtained in yields of 0.62% and 0.34%, respectively. A total of 53 compounds were identified in the leaf essential oil of C. citrinus, and 63 compounds were identified in the fruit essential oil, accounting for 99.6% and 99.4% of the compositions, respectively. Monoterpene hydrocarbons (27.6% and 53.8%) and oxygenated monoterpenoids (69.9% and 41.3%) dominated the leaf and fruit oils, respectively. The major components in C. citrinus leaf and fruit essential oils were α-pinene (18.1% and 35.1%, respectively), limonene (5.4% and 8.2%), 1,8-cineole (56.3% and 32.4%), and α-terpineol (11.2% and 5.8%) (Table 2). There have been several previous examinations of the composition of C. citrinus leaf essential oil from various geographical locations [24,25,26,27,28,29,30,31,32,33,34]. An agglomerative hierarchical cluster analysis based on the compositions of the leaf essential oils (Figure 2) reveals three well-defined clusters: (#1) 1,8-cineole >> α-pinene > α-terpineol, (#2) 1,8-cineole > α-terpineol >> eugenol, and (#3) α-pinene > 1,8-cineole > α-terpineol. The C. citrinus leaf essential oil from Vietnam (this study) falls into cluster #1.
Essential oils were obtained from six different tissues of Melaleuca leucadendra, young leaves, old leaves, stem bark, fruits, and branch tips, in yields of around 1%. A total of 104 compounds were identified in the M. leucadendra essential oils. Sesquiterpene hydrocarbons (18.8%–31.0%) and oxygenated sesquiterpenoids (35.6%–69.5%) were the dominant chemical classes. The essential oil compositions are compiled in Table 3.
Brophy has described two different chemotypes of M. leucadendra from Australia, based on leaf essential oil composition [14]. Chemotype I, from Western Australia, is rich in monoterpenoids, e.g., 1,8-cineole (10–45%), p-cymene (5–22%), α-pinene (4–19%), limonene (3–6%), and α-terpineol (6–9%). Chemotype II, from eastern Australia, is dominated by phenylpropanoids, which was divided into two subtypes: IIa, eugenol methyl ether (95%–97%), and IIb, (E)-iso-eugenol methyl ether (74%–88%) subtype). Chemotype IIa has also been represented by samples from Minas Gerais, Brazil [35], and from Lahore, Pakistan [36]. There is a third chemotype, dominated by (E)-nerolidol (>90%), which has been described from Uttarakhand, India [37] and from Pernambuco, Brazil [38]. Chemotype I has also been found in Cuba [39] and Rio de Janeiro, Brazil [40]. They were both dominated by 1,8-cineole (43.0% and 48.7%, respectively), but these two samples were also rich in viridiflorol (24.2% and 27.8%, respectively), and therefore, may represent a subtype of chemotype I.
An agglomerative hierarchical cluster analysis was carried out using the M. leucadendra leaf essential oil compositions reported in the literature [14,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50] (Figure 3). The cluster analysis reveals two sub-types of chemotype I, the two sub-types of chemotype II, as described by Brophy [14], and chemotype III, the nerolidol chemotype. The leaf essential oils of M. leucadendra from Vietnam, fall into sub-type Ib; the leaf oils were rich in α-eudesmol (17.6%–21.2%), guaiol (10.9%–12.5%), with lesser concentrations of linalool (4.9%–5.1%), (E)-caryophyllene (3.8%–7.0%), and bulnesol (3.6%–5.3%). Concentrations of 1,8-cineole were low (0.0%–5.2%), and (E)-nerolidol and viridiflorol were not observed at all.
The leaf essential oil of Syzygium nervosum was obtained in 0.2% yield. A total of 61 compounds were identified in the leaf oil of S. nervosum, accounting for 90.9% of the composition, with 31.7% monoterpene hydrocarbons, 24.3% sesquiterpene hydrocarbons, and 27.9% oxygenated sesquiterpenoids predominating. The leaf essential oil of S. nervosum was rich in (Z)-β-ocimene (20.3%), caryophyllene oxide (13.2%), (E)-caryophyllene (12.1%), and α-pinene (5.2%) (Table 4). The leaf essential oil composition is qualitatively similar, but quantitatively different, to a previous report on the leaf essential oil from Lê Mao District, Vinh City, Vietnam [51]. Both samples had relatively high concentrations of α-pinene, (Z)-β-ocimene, (E)-β-ocimene, and (E)-caryophyllene (3.7%, 32.1%, 9.4%, and 14.5%, respectively, in the Vinh City sample), but the concentration of myrcene was much higher (24.6%) in the sample from Vinh City. The leaf essential oil S. nervosum from Nepal showed a very different composition with myrcene (69.7%), (E)-β-ocimene (12.2%), (Z)-β-ocimene (4.8%), and linalool (4.1%) [52].

2.2. Mosquito Larvicidal Activity

The 24-h and 48-h larvicidal activities are presented in Table 5 and Table 6, respectively. The Myrtaceae essential oils presenting the best 24-h larvicidal activities were C. citrinus fruit essential oil (LC50 = 17.3 μg/mL against both Ae. aegypti and Cx. quinquefasciatus), M. leucadendra stem bark essential oil (LC50 = 17.1, 19.3, and 21.4 μg/mL against Ae. aegypti, Ae. albopictus, and Cx. quinquefasciatus, respectively), M. leucadendra fruit essential oil (LC50 = 13.9, 19.2, and 26.2 μg/mL against Ae. aegypti, Ae. albopictus, and Cx. quinquefasciatus, respectively), and, especially, M. leucadendra old leaf essential oil (LC50 = 7.4 and 6.6 μg/mL against Ae. aegypti and Cx. quinquefasciatus, respectively). The 48-h larvicidal activities of M. leucadendra old leaf essential oil are particularly notable with LC50 of 1.4 and 1.8 μg/mL on Ae. aegypti and Cx. quinquefasciatus.
The larvicidal activities of M. leucadendra essential oils are likely due to the high concentrations of α-eudesmol and guaiol, or possibly synergistic effects involving these compounds. Unfortunately, there appear to be no reports on the larvicidal activities of these compounds.
It is tempting to suggest that the sensitivity of mosquito larvae to C. citrinus fruit essential oil is due to the combination of α-pinene and 1,8-cineole. 1,8-Cineole, (+)-α-pinene, and (–)-α-pinene have been screened against Ae. aegypti larvae, and showed modest larvicidal activities (LC50) of 74.9, 50.9, and 64.8 μg/mL, respectively [53]. Furthermore, Hedychium bousigonianum cv. “Tai Emperor” rhizome essential oil, with 16.7% α-pinene and 25.5% 1,8-cineole, showed only marginal larvicidal activity against Ae. aegypti (80% lethality at 125 μg/mL) [54]. In addition, Pavela has shown that α-pinene has marginal larvicidal activity against Cx. quinquefasciatus (LC50 = 95 μg/mL), 1,8-cineole is inactive (LC50 > 250 μg/mL), and a binary mixture of the two compounds does not demonstrate synergistic activity [55]. The observed larvicidal activities of C. citrinus fruit essential oil is apparently due to synergistic activities involving minor components. It has been shown that Musca domestica preferentially metabolizes the major components in an essential oil, which leaves the components of lower concentrations to act as the toxic agents [56].
Baeckea frutescens and Callistemon citrinus leaf essential oils were relatively inactive against Cx. quinquefasciatus, with 24-h LC50 values of 81.7 μg/mL and 73.6 μg/mL, respectively. However, both of those essential oils showed high concentrations of α-pinene (11.1% and 18.1%, respectively) and 1,8-cineole (10.1% and 56.3%, respectively). The leaf oil of B. frutescens also had high concentrations of β-pinene (19.0%), γ-terpinene (11.7%), α-humulene (9.9%), and (E)-caryophyllene (7.1%). The relative inactivity of B. frutescens against Cx. quinquefasciatus is difficult to explain. Both β-pinene and γ-terpinene have shown good larvicidal activity against Cx. pipiens pallens with 24-h LC50 of 21.1, 12.9, and 12.6 μg/mL for (+)-β-pinene, (–)-β-pinene, and γ-terpinene, respectively [53]. (E)-Caryophyllene showed only weak larvicidal activity (LC50 = 93.7 μg/mL), however [53], and α-humulene was found to be inactive against this mosquito [57]. The major components of C. citrinus leaf essential oil and C. citrinus fruit essential oil are qualitatively similar. It is not obvious why the larvicidal activities of these two oils against Cx. quinquefasciatus are so different, but it may be due to synergistic effects of minor components present in the fruit essential oil but absent in the leaf essential oil. Apparently, there is more involved in the larvicidal activities of these essential oils than the major components.
Syzygium nervosum essential oil larvicidal activity is also difficult to explain. There were high concentrations of (Z)-β-ocimene (20.3%), (E)-caryophyllene (12.1%), and caryophyllene oxide (13.2%). Unfortunately, we have found no larvicidal screening of (Z)-β-ocimene in the literature. Note, however, that Syzygium jambolana essential oil, rich in (Z)-β-ocimene (27.2%), was inactive against Ae. aegypti larvae (LC50 = 433 μg/mL) [58]. Furthermore, (E)-caryophyllene and caryophyllene oxide have shown only marginal larvicidal activities against Ae. aegypti or Cx. pipiens pallens [53,57].

2.3. Antimicrobial Activity

The Myrtaceae essential oils were screened for antibacterial activity against Enterococcus faecalis (ATCC 29912) and Staphylococcus aureus (ATCC 25923), and for antifungal activity against Candida albicans (ATCC 10231). The antimicrobial activities are summarized in Table 7.
The leaf essential oils of B. frutescens and C. citrinus both showed excellent anti-Candida activity, with minimum inhibitory concentration (MIC) values of 16 μg/mL. van Zyl and co-workers have screened several monoterpenoids against C. albicans, and many of the major components that were found in B. frutescens and C. citrinus leaf essential oils did show notable activities, including α-pinene (MIC 12.0 μg/mL), β-pinene (MIC 1.0 μg/mL), limonene (MIC 10.0 μg/mL), and γ-terpinene (MIC 6.0 μg/mL) [59]. 1,8-Cineole and α-terpineol are relatively inactive against C. albicans, however [60,61]. A perusal of the literature reveals a broad spectrum of reported antimicrobial activities for terpenoid constituents against E. faecalis, S. aureus, and C. albicans (Table 8). There are several potential reasons for the apparent discrepancies, including variation in antimicrobial assay protocols, different susceptibilities of different strains of a particular microorganism, mathematical errors in calculating dilutions and MIC values.
Callistemon citrinus fruit essential oil, dominated by α-pinene (35.1%) and 1,8-cineole (32.4%), was particularly active against E. faecalis. Neither of these compounds have shown notable activity against E. faecalis, however (Table 8); the activity observed for C. citrinus fruit essential oil must be attributed to synergistic activity of less abundant components. Melaleuca leucadendra bark essential oil, which was rich in α-eudesmol (24.1%) and guaiol (11.3%), also exhibited notable activity against E. faecalis, possibly due to the high concentrations of sesquiterpene alcohols present.

3. Materials and Methods

3.1. Plant Collection

Plant materials were collected from wild-growing plants in the Hoa Vang and Hoa Khanh districts of Da Nang city. The plants were identified by Do Ngoc Dai. In each case, the fresh plant material was chopped, and 2.0 kg was subjected to hydrodistillation using a Clevenger-type apparatus (Table 9).

3.2. Gas Chromatographic – Mass Spectral Analysis

Each of the essential oils was analyzed by gas chromatography-mass spectrometry (GC-MS), as previously reported [81], using a Shimadzu GCMS-QP2010 Ultra, fitted with a ZB-5 column. Identification of the oil components was based on their retention indices determined by reference to a homologous series of n-alkanes, and by comparison of their mass spectral fragmentation patterns with those in the NIST [21] and FFSNC [22] databases and our own Sat-Set library [23].

3.3. Mosquito Larvicidal Assays

Mosquito colonies of Aedes aegypti, Aedes albopictus, and Culex quinquefasciatus were obtained and maintained as previously described [82].
Larvicidal activities of the essential oils were evaluated according to the protocol of Liu and co-workers [83] with slight modifications. For each assay, 150 mL of water containing 20 fourth-instar mosquito larvae was placed into 250-mL beakers and aliquots of the essential oils dissolved in EtOH (1% stock solution) were then added. A set of controls using EtOH only (negative control) and permethrin (positive control) were included for comparison. Mortality was recorded after 24 h and after 48 h of exposure, during which no nutritional supplement was added. The experiments were carried out at 25 ± 2 °C. Each test was conducted in quadruplicate with five concentrations (100, 50, 25, 12.5 and 6 μg/mL). The data obtained were subjected to log-probit analysis [84] to obtain LC50 values, LC90 values and 95% confidence limits using Minitab® 19 (Minitab, LLC, State College, PA, USA).

3.4. Antimicrobial Screening

The antimicrobial activity of the essential oils was evaluated using two bacteria (Enterococcus faecalis, ATCC 299212, and Staphylococcus aureus, ATCC 25923) and one yeast (Candida albicans, ATCC 10231) using the microdilution broth susceptibility assay, as previously reported [82]. Stock solutions of the each of the essential oils were prepared in dimethylsulfoxide. Dilution series were prepared from 16,384 to 2 μg/mL (214, 213, 212, 211, 210, 29, 27, 25, 23 and 21 µg/mL) in sterile distilled water in micro-test tubes from where they were transferred to the 96-well microtiter plates for the assays.

3.5. Agglomerative Hierarchical Cluster Analysis

The essential oil compositions from this work and from the published literature were treated as operational taxonomic units (OTUs). The percentage composition of the major components of the essential oils was used to determine the chemical relationship between the various essential oil samples by agglomerative hierarchical cluster (AHC) analysis, using the XLSTAT software, version 2018.1.1.6097 (Addinsoft™, Paris, France). Euclidean distance was used to measure dissimilarity, and Ward’s method was used for cluster definition.

4. Conclusions

Essential oils derived from Baeckea frutescens, Callistemon citrinus, Melaleuca leucadendra, and Syzygium nervosum have shown larvicidal activities against the mosquito species tested. In most cases, the larvicidal activities cannot be attributed to the major components, and synergistic interactions with minor components are likely responsible. Likewise, all of the Myrtaceae essential oils examined for antimicrobial activity showed promise. Thus, these essential oils may serve as “green” vector control agents and/or complementary antimicrobial agents, as well as providing value-added commodities for harvested timbers (e.g., Melaleuca leucadendra).

Author Contributions

Conceptualization, N.H.H.; methodology, N.H.H., P.S., W.N.S., N.T.G.A., D.N.D; software, P.S.; validation, N.H.H., P.S., and W.N.S.; formal analysis, W.N.S.; investigation, N.T.G.A., L.T.H., T.A.T., N.H.H., D.N.D., N.T.B.N.; resources, N.H.H. and P.S.; data curation, W.N.S.; writing—original draft preparation, W.N.S.; writing—review & editing, N.H.H., P.S., and W.N.S.; visualization, W.N.S.; supervision, N.H.H.; project administration, N.H.H.; funding acquisition, N.H.H. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Duy Tan University.

Acknowledgments

P.S. and W.N.S. participated in this work as part of the activities of the Aromatic Plant Research Center (APRC, https://aromaticplant.org/).

Conflicts of Interest

The authors declare no conflict of interest.

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Plants 09 00544 g001a 550Plants 09 00544 g001b 550
Figure 1. Photographs of the plants examined in this work. A: Baeckea frutescens, B: Callistemon citrinus, C: Syzygium nervosum, D: Melaleuca leucadendra.
Figure 1. Photographs of the plants examined in this work. A: Baeckea frutescens, B: Callistemon citrinus, C: Syzygium nervosum, D: Melaleuca leucadendra.
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Plants 09 00544 g002 550
Figure 2. Dendrogram obtained from the agglomerative hierarchical cluster analysis of Callistemon citrinus leaf essential oil compositions.
Figure 2. Dendrogram obtained from the agglomerative hierarchical cluster analysis of Callistemon citrinus leaf essential oil compositions.
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Plants 09 00544 g003 550
Figure 3. Dendrogram obtained from the agglomerative hierarchical cluster analysis of Melaleuca leucadendra leaf essential oil compositions.
Figure 3. Dendrogram obtained from the agglomerative hierarchical cluster analysis of Melaleuca leucadendra leaf essential oil compositions.
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Table
Table 1. Chemical composition of Baeckea frutescens leaf essential oil from central Vietnam.
Table 1. Chemical composition of Baeckea frutescens leaf essential oil from central Vietnam.
RI(calc)RI(db)Compounds%RI(calc)RI(db)Compounds%
922927α-Thujene1.813701375α-Copaene0.2
930933α-Pinene11.113981405(Z)-Caryophyllenetr
943948α-Fenchene tr14011406α-Gurjunenetr
945953Camphene0.114151417(E)-Caryophyllene7.1
968972Sabinenetr14331438Aromadendrene0.1
975978β-Pinene19.014521454α-Humulene9.9
984991Myrcene0.314551457allo-Aromadendrene0.1
10001004p-Mentha-1(7),8-dienetr14661472trans-Cadina-1(6),4-diene0.1
10031007α-Phellandrene0.114691478γ-Muurolenetr
10051009δ-3-Carenetr14831487β-Selinene 0.1
10131018α-Terpinene 0.314851490γ-Amorphenetr
10211025p-Cymene8.914901501α-Selinene 0.1
10251030Limonene1.714921497α-Muurolene 0.1
102910301,8-Cineole10.115001507Geranyl isobutyrate0.1
10301034(Z)-β-Ocimenetr15061512γ-Cadinene0.2
10411045(E)-β-Ocimenetr15091519Cubeboltr
10551057γ-Terpinene11.715121518δ-Cadinene 0.9
10651069cis-Linalool oxide (furanoid)tr15151519trans-Calamenene0.1
10811086Terpinolene0.715161521Zonarene0.1
10851093p-Cymenenetr15261536trans-Cadine-1,4-diene 0.1
10961101Linalool4.415301538α-Cadinene tr
10981104Hotrienoltr15341544α-Calacorenetr
11141119endo-Fenchol0.115411549α-Elemoltr
11331139Nopinonetr15451551(Z)-Caryphyllene oxide0.1
11361141trans-Pinocarveoltr15541562(E)-Nerolidol0.5
11501156Camphene hydratetr15701576Spathulenoltr
11651170δ-Terpineol 0.115761587Caryophyllene oxide2.0
11671170Borneol0.115791590Globulol0.1
11691171cis-Linalool oxide (pyranoid)tr15921592Humulene epoxide I0.3
117311792-Isopropenyl-5-methyl-4-hexenal0.115981605Ledol0.1
11761180Terpinen-4-ol0.716041613Humulene epoxide II2.4
11781188Naphthalenetr16191624Muurola-4,10(14)-dien-1β-oltr
11811186p-Cymen-8-oltr162116281-epi-Cubenol0.3
11901195α-Terpineol 1.716251611Germacra-1(10),5-dien-4α-ol0.3
11981203p-Cumenoltr16261632Humulenol II0.3
12191229Nerol tr16301636Caryophylla-4(12),8(13)-dien-5β-ol0.1
12341240Ascaridoletr16341643τ-Cadinol 0.2
12441244Geraniol0.116361645τ-Muurolol0.1
12611268Geranialtr16391651α-Muurolol (= δ-Cadinol)0.1
12681275trans-Ascaridol glycoltr16481652α-Eudesmol0.5
12741284p-Cymen-7-oltr18411837Homoisobaeckeol0.5
12841289Thymoltr Monoterpene hydrocarbons55.6
12911399Carvacroltr Oxygenated monoterpenoids17.5
12981306Isoascaridoletr Sesquiterpene hydrocarbons19.1
13141320Methyl geranate0.1 Oxygenated sesquiterpenoids7.3
13411349α-Cubebenetr Benzenoid aromatics0.5
13441357Eugenoltr Otherstr
Total identified100.0
RI(calc): Retention indices determined with respect to a homologous series of n-alkanes on a ZB-5ms column. RI(db): Retention indices obtained from the databases [21,22,23]. tr: trace (< 0.05%).
Table
Table 2. Chemical compositions of the leaf and fruit essential oils of Callistemon citrinus from central Vietnam.
Table 2. Chemical compositions of the leaf and fruit essential oils of Callistemon citrinus from central Vietnam.
RI(calc)RI(db)Compound% Composition
Leaf Fruit
7937912,4-Dimethyl-3-pentanone 0.3tr
912913Isobutyl isobutyrate0.20.3
924927α-Thujene 0.30.8
932933α-Pinene18.135.1
946948α-Fenchenetrtr
948953Camphene0.10.1
971972Sabinenetrtr
976978β-Pinene 0.60.7
987989Myrcene0.10.5
9991000δ-2-Carenetr0.1
10041004p-Mentha-1(7),8-diene0.10.1
10061007α-Phellandrene 0.41.6
10081009δ-3-Carene0.10.1
10111014Isoamyl isobutyrate0.20.3
10141018α-Terpinene---0.2
101410152-Methylbutyl isobutyratetr0.1
10211022Ethyl 3-methylbut-3-enyl carbonate0.10.1
10241025p-Cymene2.24.6
10291030Limonene5.48.2
103010321,8-cineole56.332.4
10321034(Z)-β-Ocimene ---0.1
10441046(E)-β-Ocimene tr0.2
10511050Prenyl isobutyratetr0.1
10571057γ-Terpinene0.31.0
10841087Terpinolene0.10.6
10881093p-Cymenene---0.1
10991101Linalool0.51.4
11191119endo-Fenchol0.10.1
11401141trans-Pinocarveol0.3tr
11551156Camphene hydratetrtr
11631164Pinocarvonetr---
11701170δ-Terpineol 0.20.1
11701165iso-Borneol---0.1
11731173Borneol0.10.1
117911792-Isopropenyl-5-methyl-4-hexenal0.1tr
11801180Terpinen-4-ol0.50.6
11851188Naphthalene0.1---
11861189p-Cymen-8-ol ---tr
11881187trans-p-Mentha-1(7),8-dien-2-ol 0.1---
11941195α-Terpineol11.25.8
12021202cis-Sabinol---0.1
12191223trans-Carveol0.1tr
12301230cis-p-Mentha-1(7),8-dien-2-ol tr---
12491249Geraniol0.50.6
12981300Carvacroltr0.1
13511356Eugenol0.10.1
13851390β-Elemene---0.1
13921395Phenylethyl isobutyratetrtr
14171417(E)-Caryophyllene 0.10.2
14361438Aromadendrene0.10.2
14521454α-Humulene---0.1
14581458allo-Aromadendrene0.10.1
14771480Germacrene D---tr
14871491Viridiflorene---0.1
15001503(E,E)-α-Farnesene---0.1
15051507Geranyl isobutyrate0.1---
15051508β-Bisabolene---0.1
15141518δ-Cadinene---tr
15351539Flavesone0.30.3
15571561(E)-Nerolidol---0.1
15751578Spathulenol0.41.3
15801577Caryophyllene oxidetr0.1
15841590Globulol0.10.2
15931594Viridiflorol0.10.1
15951599Cubeban-11-oltr0.1
16091614iso-Leptospermonetr0.1
16191626Leptospermonetr0.2
16291629iso-Spathulenol---0.2
Monoterpene hydrocarbons27.653.8
Oxygenated monoterpenoids69.941.3
Sesquiterpene hydrocarbons0.20.8
Oxygenated sesquiterpenoids0.52.0
Others1.41.4
Total identified99.699.4
RI(calc): Retention indices determined with respect to a homologous series of n-alkanes on a ZB-5ms column. RI(db): Retention indices obtained from the databases [21,22,23]. tr: trace (<0.05%).
Table
Table 3. Chemical compositions of essential oils from Melaleuca leucadendra from central Vietnam.
Table 3. Chemical compositions of essential oils from Melaleuca leucadendra from central Vietnam.
RI(calc)RI(db)Compound% Composition
Young LeafOld LeafStem BarkFruitBranch Tips
923927α-Thujene0.80.40.1tr1.2
931933α-Pinene0.70.60.80.21.4
947953Camphene---trtrtr---
960960Benzaldehyde0.10.1------tr
975978β-Pinene0.10.20.30.10.1
987991Myrcene0.20.30.20.10.2
10031004p-Mentha-1(7),8-diene------tr------
10051007α-Phellandrene0.30.2------0.3
10071009δ-3-carene0.1trtr---0.1
10151018α-Terpinene 0.40.3------0.4
10231025p-Cymene3.91.71.30.58.7
10271030Limonene0.30.81.40.40.7
10291031β-Phellandrenetr0.1tr---0.1
103010301,8-cineole---5.21.80.2tr
10331034(Z)-β-Ocimene---tr------tr
10431045(E)-β-Ocimene---tr------tr
10561057γ-Terpinene2.21.3tr---3.3
10681069cis-Linalool oxide (furanoid)------------tr
10841086Terpinolene3.01.60.1tr4.4
10891093p-Cymenene0.1trtr---0.2
10991101Linalool4.95.11.40.44.2
11031107Nonanal------0.1------
111011101,3,8-p-Menthatrienetrtr---------
11221124cis-p-Menth-2-en-1-oltrtr---------
11411142Epoxyterpinolene0.3tr------0.6
11471149iso-Pulegol---tr------tr
11681170δ-Terpineol---tr---------
11701170Borneol---tr---------
117711792-Isopropenyl-5-methyl-4-hexenal0.20.1------0.3
11791180Terpinen-4-ol0.90.4trtr1.1
11831188Naphthalene------0.10.10.2
118411884’-Methylacetophenone0.1tr------0.1
11861188p-Cymen-8-ol1.00.20.10.11.2
11941195α-Terpineol0.71.80.50.10.6
11981195p-Menth-3-en-7-al------------0.1
12021203p-Cumenol0.10.1------0.1
12221222iso-Ascaridol---tr------0.1
12231226Nerol---trtr------
12251227Citronellol---trtrtr0.1
12481249Geraniol0.20.60.40.10.2
12661266Geranial---trtr------
12731275trans-Ascaridol glycol0.2tr------0.1
12901291cis-Ascaridol glycol0.1---------0.1
12931305Benzophenone----tr---------
131813183-Hydroxycineole0.2---------0.1
13481356Eugenol---0.1---------
13671371α-Ylangene0.40.60.90.60.7
13731375α-Copaene0.20.30.80.30.3
13751380Geranyl acetate---0.10.2tr0.1
13811382β-Bourbonene------tr------
13871390β-Elemene0.10.10.1tr0.1
13891394Sativene0.10.10.1tr0.1
14011405(Z)-Caryophyllene------trtr---
14171417(E)-Caryophyllene3.87.05.54.35.7
142114288-Hydroxycarvotanacetone0.1---------0.1
14261427γ-Elemene 0.20.30.10.10.1
14321436α-Guaiene0.10.20.20.20.2
14381444Guaia-6,9-diene0.20.20.10.10.2
14441448cis-Muurola-3,5-diene 0.20.20.10.10.2
14461447iso-Germacrene D0.10.20.10.10.2
14531454α-Humulene 2.84.43.52.83.7
14671473Drima-7,9(11)-diene0.10.20.20.20.2
14701476Selina-4,11-diene0.20.50.50.40.6
14741476γ-Gurjunene 0.61.11.10.91.4
14761479α-Amorphene 0.71.21.50.91.2
14841488δ-Selinene1.01.60.70.61.3
14871492β-Selinene 2.43.74.83.14.2
14901490γ-Amorphene 0.20.30.40.30.5
14941501α-Selinene 2.13.73.62.54.1
14951496trans-Muurola-4(14),5-diene---0.2------0.1
14961497α-Muurolene------0.20.1---
14991505α-Bulnesene ---0.10.10.20.1
14991506δ-Amorphene---0.2---------
15001502trans-β-Guaiene---0.3---------
15011501β-Dihydroagarofuran ------0.20.2---
15151518δ-Cadinene ------0.20.1---
151615207-epi-α-Selinene---------0.2---
15171519trans-Calamenene ------0.70.4---
15341540Selina-4(15),7(11)-diene0.50.60.60.60.7
15391541α-Calacorene0.30.60.80.50.6
15391546Selina-3,7(11)-diene0.30.2---0.30.3
15451546α-Elemol 0.30.10.30.4---
15561557Germacrene B0.40.40.1---0.1
15801587Caryophyllene oxide1.82.33.33.24.0
15901600Khusimone0.20.30.40.30.3
15951603Guaiol12.510.911.310.47.3
16071613Humulene epoxide II0.80.91.51.31.6
16101609Rosifoliol0.50.40.50.50.2
16201611Germacra-1(10),5-dien-4α-ol0.20.20.2---0.2
16231624Selina-6-en-4β-ol 2.01.61.72.21.2
16241629iso-Spathulenol 0.2------------
16281631Eremoligenol3.43.44.96.52.7
16301633γ-Eudesmol 3.92.83.55.31.9
16321634cis-Cadin-4-en-7-ol 3.53.03.33.52.2
16351636Caryophylla-4(12),8(13)-dien-5β-ol---0.20.20.10.2
16381645Hinesol1.00.91.21.60.7
16451644Selina-3,11-dien-6α-ol---0.20.3---0.2
16531652α-Eudesmol21.217.624.130.713.7
16571660Selin-11-en-4α-ol1.91.51.31.61.0
16631673Bulnesol5.33.63.34.42.2
1668167114-Hydroxy-9-epi-(E)-caryophyllene ------0.5------
16701677Cadalene------0.30.2---
16951696Juniper camphor---0.20.10.20.1
19181929Carissone------0.10.4---
Monoterpene hydrocarbons11.97.24.21.321.2
Oxygenated monoterpenoids8.813.54.40.89.0
Sesquiterpene hydrocarbons18.830.830.523.431.0
Oxygenated sesquiterpenoids56.947.659.169.535.6
Benzenoid aromatics0.20.10.00.00.1
Others0.00.00.20.10.2
Total identified96.699.398.495.297.1
RI(calc): Retention indices determined with respect to a homologous series of n-alkanes on a ZB-5ms column. RI(db): Retention indices obtained from the databases [21,22,23]. tr: trace (<0.05%).
Table
Table 4. Chemical compositions of essential oils from Syzygium nervosum from central Vietnam.
Table 4. Chemical compositions of essential oils from Syzygium nervosum from central Vietnam.
RI(calc)RI(db)Compound%RI(calc)RI(db)Compound%
930933α-Pinene5.214861492β-Selinene 0.9
968971Tetrahydrofurfuryl acetate0.214921501α-Selinene 0.9
975978β-Pinene1.014941500α-Muurolene 0.4
986991Myrcene0.415091512γ-Cadinene0.9
10221025p-Cymene0.115141518δ-Cadinene 1.0
10271030Limonene0.215331538α-Cadinene0.4
10331034(Z)-β-Ocimene20.315381541α-Calcorene0.4
10431045(E)-β-Ocimene3.515571560(E)-Nerolidol 0.1
10891091Rosefuran0.715591560β-Calacorene0.5
10921101α-Pinene oxide1.315731576Spathulenol0.6
10971101Linalool0.315791587Caryophyllene oxide13.2
110111026-Methyl-3,5-heptadien-2-one0.515821590Globulol1.2
11251127allo-Ocimene0.815911592Viridiflorol0.4
11271128(Z)-Epoxy ocimene (= (Z)-Myroxide)0.515931593Guaiol0.5
11371137(E)-Epoxy ocimene (= (E)-Myroxide)0.415951592Humulene epoxide I0.2
11671169Rosefuran epoxide0.316031607β-Oplopenone0.8
11701171p-Mentha-1,5-dien-8-ol0.216061613Humulene epoxide II1.8
11821188Naphthalene0.416231624Selina-6-en-4β-ol 3.4
11931195α-Terpineol0.1162416281-epi-Cubenol 0.6
1199---(3Z)-Octenyl acetate 0.416311634cis-Cadin-4-en-7-ol 0.4
11991205cis-4-Caranone0.116341636Caryophylla-4(12),8(13)-dien-5β-ol0.5
12061207(3E)-Octenyl acetate 0.716381643τ-Cadinol 0.7
13531349α-Terpinyl acetate0.716401644τ-Muurolol 0.2
13661367Cyclosativene0.216431651α-Muurolol (= δ-Cadinol)0.2
13721375α-Copaene0.416451645Selina-3,11-dien-6α-ol0.4
13741380Geranyl acetate0.416521655α-Cadinol 1.7
14171417(E)-Caryophyllene 12.116551660Selin-11-en-4α-ol0.6
14261433β-Copaene0.316981697(E)-trans-α-Bergamota-2,10-dien-12-ol0.4
14351438Aromadendrene0.6 Monoterpene hydrocarbons31.7
14521454α-Humulene 2.7 Oxygenated monoterpenoids4.9
14711478γ-Muurolene0.9 Sesquiterpene hydrocarbons24.3
14731476γ-Gurjunene 1.4 Oxygenated sesquiterpenoids27.9
14751482α-Amorphene 0.3 Others2.1
Total identified90.9
RI(calc): Retention indices determined with respect to a homologous series of n-alkanes on a ZB-5ms column. RI(db): Retention indices obtained from the databases [21,22,23].
Table
Table 5. Twenty-four-hour mosquito larvicidal activities of Myrtaceae essential oils.
Table 5. Twenty-four-hour mosquito larvicidal activities of Myrtaceae essential oils.
Essential OilLC50 (95% Fiducial Limits)LC90 (95% Fiducial Limits)χ2p
Aedes aegypti
Baeckea frutescens leaf EO23.00 (20.38–25.75)40.05 (35.75–46.71)6.5120.039
Callistemon citrinus leaf EO22.37 (18.62–25.88)57.34 (50.00–69.06)0.66550.717
Callistemon citrinus fruit EO17.27 (15.30–19.03)33.02 (29.82–38.04)0.43480.805
Melaleuca leucadendra young leaf EOntnt------
Melaleuca leucadendra old leaf EO7.400 (6.308–8.612)18.29 (16.05–21.47)30.770.000
Melaleuca leucadendra stem bark EO17.14 (14.73–19.21)36.25 (32.42–42.31)2.2440.326
Melaleuca leucadendra fruit EO13.90 (11.03–16.02)31.76 (28.40–37.25)0.57500.750
Melaleuca leucadendra branch tip EO21.99 (19.80–24.57)37.63 (33.67–43.39)2.2770.517
Syzygium nervosum leaf EO28.63 (24.83–32.87)61.41 (53.99–72.38)3.7920.285
Aedes albopictus
Baeckea frutescens leaf EO25.73 (23.68–28.39)37.01 (33.33–43.13)0.42090.810
Callistemon citrinus leaf EOntnt------
Callistemon citrinus fruit EOntnt------
Melaleuca leucadendra young leaf EOntnt------
Melaleuca leucadendra old leaf EOntnt------
Melaleuca leucadendra stem bark EO19.31 (16.83–21.60)40.91 (36.56–47.59)0.59860.741
Melaleuca leucadendra fruit EO19.17 (16.89–21.32)39.08 (34.96–45.47)4.74200.093
Melaleuca leucadendra branch tip EOntnt------
Syzygium nervosum leaf EOntnt------
Culex quinquefasciatus
Baeckea frutescens leaf EO81.72 (76.16–87.75112.7 (104.7–123.6)3.0970.078
Callistemon citrinus leaf EO73.60 (64.87–85.83)172.2 (135.9–249.1)57.100.000
Callistemon citrinus fruit EO17.30 (11.04–22.56)77.42 (66.07–95.50)63.930.000
Melaleuca leucadendra young leaf EO46.62 (42.65–51.45)70.10 (62.93–82.10)0.20830.648
Melaleuca leucadendra old leaf EO6.618 (3.635–9.183)32.80 (27.99–40.13)5.4740.361
Melaleuca leucadendra stem bark EO21.35 (13.62–28.02)100.2 (84.4–126.2)86.780.000
Melaleuca leucadendra fruit EO26.20 (19.47–32.30)91.81 (78.04–114.46)46.320.000
Melaleuca leucadendra branch tip EO43.69 (40.13–47.81)64.43 (58.27–74.71)0.021810.883
Syzygium nervosum leaf EO46.09 (40.59–52.38)95.07 (84.44–109.96)1.0610.786
LC50 and LC90 in μg/mL. nt = not tested.
Table
Table 6. Forty-eight-hour mosquito larvicidal activities of Myrtaceae essential oils.
Table 6. Forty-eight-hour mosquito larvicidal activities of Myrtaceae essential oils.
Essential OilLC50 (95% Confidence Limits)LC90 (95% Confidence Limits)χ2p
Aedes aegypti
Baeckea frutescens leaf EO15.31 (11.25–18.31)34.69 (30.31–42.30)2.4180.298
Callistemon citrinus leaf EO21.60 (17.74–25.13)56.87 (49.55–68.64)1.1040.576
Callistemon citrinus fruit EO16.80 (14.85–18.50)31.91 (28.87–36.66)0.24930.883
Melaleuca leucadendra young leaf EOntnt------
Melaleuca leucadendra old leaf EO1.379 (1.127–1.626)5.066 (4.173–6.551)119.90.000
Melaleuca leucadendra stem bark EO13.96 (10.91–16.21)33.15 (29.54–39.08)1.1150.573
Melaleuca leucadendra fruit EO9.071 (3.729–12.276)30.90 (27.21–37.34)1.1800.554
Melaleuca leucadendra branch tip EO15.79 (14.01–17.73)28.64 (25.53–33.35)2.1030.551
Syzygium nervosum leaf EO11.97 (5.54–16.89)53.97 (45.87–67.18)5.7460.125
Aedes albopictus
Baeckea frutescens leaf EO23.98 (21.76–26.57)37.63 (33.75–43.80)1.3750.503
Callistemon citrinus leaf EOntnt------
Callistemon citrinus fruit EOntnt------
Melaleuca leucadendra young leaf EOntnt------
Melaleuca leucadendra old leaf EOntnt------
Melaleuca leucadendra stem bark EO17.09 (14.89–19.01)34.53 (31.02–40.08)1.0500.592
Melaleuca leucadendra fruit EO17.34 (14.79–19.55)37.85 (33.75–44.37)3.94400.139
Melaleuca leucadendra branch tip EOntnt------
Syzygium nervosum leaf EOntnt------
Culex quinquefasciatus
Baeckea frutescens leaf EO64.06 (56.83–72.12)116.6 (103.4–137.2)4.9370.026
Callistemon citrinus leaf EO49.18 (39.75–60.67)227.8 (147.4–549.1)16.790.000
Callistemon citrinus fruit EO16.02 (12.54–19.77)72.19 (60.64–91.68)61.560.000
Melaleuca leucadendra young leaf EO30.37 (21.56–36.81)72.32 (63.07–88.25)4.5610.033
Melaleuca leucadendra old leaf EO1.819 (1.262–2.394)14.40 (11.04–20.43)30.790.000
Melaleuca leucadendra stem bark EO12.02 (5.71–16.91)64.16 (55.04–78.56)55.710.000
Melaleuca leucadendra fruit EO17.38 (12.96–21.46)88.42 (65.61–143.30)17.230.000
Melaleuca leucadendra branch tip EO23.78 (12.17–31.00)66.12 (57.18–82.37)2.3830.123
Syzygium nervosum leaf EO22.74 (16.64–28.33)75.02 (64.50–91.30)11.250.010
LC50 and LC90 in μg/mL. nt = not tested.
Table
Table 7. Antimicrobial activities of Myrtaceae essential oils.
Table 7. Antimicrobial activities of Myrtaceae essential oils.
SampleEnterococcus faecalisStaphylococcus aureusCandida albicans
MIC (μg/mL)
Baeckea frutescens leaf EO64nt16
Callistemon citrinus leaf EO3225616
Callistemon citrinus fruit EO16nt128
Melaleuca leucadendra old leaf EO3264128
Melaleuca leucadendra stem bark EO166464
Melaleuca leucadendra fruit EO3264256
Syzygium nervosum leaf EO32nt128
Streptomycin256256nt
Nistatinntnt8
IC50 (μg/mL)
Baeckea frutescens leaf EO33.56nt8.67
Callistemon citrinus leaf EO16.67128.008.67
Callistemon citrinus fruit EO8.89nt32.67
Melaleuca leucadendra old leaf EO16.7233.2365.56
Melaleuca leucadendra stem bark EO8.3232.2334.22
Melaleuca leucadendra fruit EO15.9832.89128.35
Syzygium nervosum leaf EO17.00nt65.33
MIC = minimum inhibitory concentration, EO = essential oil, nt = not tested, IC50 = median inhibitory concentration.
Table
Table 8. Antimicrobial activities (MIC, μg/mL) of essential oil components from the literature.
Table 8. Antimicrobial activities (MIC, μg/mL) of essential oil components from the literature.
CompoundEnterococcus faecalis [Ref]Staphylococcus aureus [Ref]Candida albicans [Ref]
α-pinene8000 [62]
>4000 [63]
inactive [64]		13.6 [65]
45.7 [66]
312 [60]
800 [62]
1600 [67]
1300–2500 [68]
>32 [59]		12 [59]
156 [60]
800 [67]
>1000 [69]
β-pinene60 [70]
2500 [71]
>4000 [63]		3.0 [59]
41.3 [66]
600 [70]
1600 [67]
>20 [65]		1.0 [59]
60 [70]
100 [69]
1600 [67]
p-cymene600 [72]
inactive [73]		2000 [67]
>32 [59]
>10,000 [68]
>80,000 [74] 		100 [69]
1600 [67]
>32 [59]
>80,000 [61]
limonene27,000 [75]24 [59]
32.1 [66]
312 [60]
>20 [65]
>10,000 [68]		10 [59]
1000 [69]
1250 [60]
1,8-cineole7500 [64]
23,000 [75]
>8000 [76]
inactive [62]		32 [59]
625 [60]
5000 [74]
>10,000 [68]		312 [60]
10,000 [74]
40,000 [61]
>32 [59]
>1000 [69]
γ-terpineneno data>32 [59]
>80,000 [74]		6.0 [59]
100 [69]
>80,000 [61]
α-terpineol>1000 [77]1250 [60]
2500 [74]
>20 [65]		1200 [61]
1250 [60]
2500 [74]
(E)-caryophyllene6 [78]
60 [70]
2500 [71]
>4000 [63]
inactive [79]		5.1 [65]
30.3 [66]
60 [78]
312 [60]
9100 [79]
>10,000 [68]		1250 [60]
>1000 [69]
inactive [78]
inactive [79]
α-humulene6 [70]
>400 [80]		2.6 [65]
312 [60]
>10,000 [68]
inactive [70]		625 [60]
inactive [70]
Table
Table 9. Collection details and essential oil yields of four species of Myrtaceae from central Vietnam.
Table 9. Collection details and essential oil yields of four species of Myrtaceae from central Vietnam.
SpeciesVietnamese NameCollection SiteVoucher NumberPart% Yield
Baeckea frutescens L.Chổi xể, Chổi trện, Chóp máu, Thanh hao, Thanh liễuHoa Vang district, Da Nang city (16°1′10.1″ N, 108°06′01.3″ E, elev. 27 m), in January 2019.NHH7Leaf2.23
Melaleuca leucadendra (L.) L.Tràm lá dài, tràm lá hẹpHoa Vang district, Da Nang city (16°1′10.1″ N, 108°06′01.3″ E, elev. 27 m), in February 2019.NHH4Young leaf1.22
Old leaf1.43
Stem bark0.91
Fruit1.12
Branch tip1.10
Callistemon citrinus (Curtis) SkeelsTràm bông đỏ, Tràm liễu, Kiều nhụy, Kiều hùngGarden for Medicinal Plant Conservation, Duy Tan University, Hoa Khanh district, Da Nang city (16°02′57.6″ N, 108°09′34.5″ E, elev 8 m), in November 2018.NHH6Leaf0.62
Fruit0.34
Syzygium nervosum DC. Vối, Trâm vối, Trâm nắpGarden for Medicinal Plant Conservation, Duy Tan University, Hoa Khanh district, Da Nang city (16°02′57.6″ N, 108°09′34.5″ E, elev. 8 m), in January 2019.NHH10Leaf0.20

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An, N.T.G.; Huong, L.T.; Satyal, P.; Tai, T.A.; Dai, D.N.; Hung, N.H.; Ngoc, N.T.B.; Setzer, W.N. Mosquito Larvicidal Activity, Antimicrobial Activity, and Chemical Compositions of Essential Oils from Four Species of Myrtaceae from Central Vietnam. Plants 2020, 9, 544. https://0-doi-org.brum.beds.ac.uk/10.3390/plants9040544

AMA Style

An NTG, Huong LT, Satyal P, Tai TA, Dai DN, Hung NH, Ngoc NTB, Setzer WN. Mosquito Larvicidal Activity, Antimicrobial Activity, and Chemical Compositions of Essential Oils from Four Species of Myrtaceae from Central Vietnam. Plants. 2020; 9(4):544. https://0-doi-org.brum.beds.ac.uk/10.3390/plants9040544

Chicago/Turabian Style

An, Nguyen Thi Giang, Le Thi Huong, Prabodh Satyal, Thieu Anh Tai, Do Ngoc Dai, Nguyen Huy Hung, Nguyen Thi Bich Ngoc, and William N. Setzer. 2020. "Mosquito Larvicidal Activity, Antimicrobial Activity, and Chemical Compositions of Essential Oils from Four Species of Myrtaceae from Central Vietnam" Plants 9, no. 4: 544. https://0-doi-org.brum.beds.ac.uk/10.3390/plants9040544

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