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Review

Development of Pinaceae and Cupressaceae Essential Oils from Forest Waste in South Korea

1
College of Forest and Environmental Sciences, Kangwon National University, Chuncheon 24341, Republic of Korea
2
Forest Industrial Materials Division, Forest Products and Industry Department, National Institute of Forest Science, Seoul 02455, Republic of Korea
*
Author to whom correspondence should be addressed.
Plants 2023, 12(19), 3409; https://doi.org/10.3390/plants12193409
Submission received: 21 August 2023 / Revised: 15 September 2023 / Accepted: 18 September 2023 / Published: 27 September 2023

Abstract

:
The growing awareness of environmental issues has garnered increasing interest in the use of waste material in a wide variety of applications. From this viewpoint, developing essential oils from forest waste can bring new cost opportunities for the effective and sustainable management of unused forestry biomass. However, better knowledge of the production, chemical constituents, and application of essential oils is necessary. Among the species considered to be of interest from the point of view of their essential oils and forest biomass, Pinaceae and Cupressaceae were selected in this study as potential candidates for commercial essential oils based on previous studies. This current study focuses on investigating Pinaceae (Larix kaempferi, Pinus densiflora, and Pinus koraiensis) and Cupressaceae (Chamaecyparis obtusa and Chamaecyparis pisifera) essential oils extracted from various parts from the perspective of their bioactive compounds and potential applications. This is followed by an overview of the essential oils industry in South Korea, with particular attention being paid to utilising unused forest biomass. Therefore, this is a comprehensive review suggesting that Pinaceae and Cupressaceae essential oils extracted from various parts of forest waste could be utilised in various industries, adding value to the aspect of sustainable industry. Furthermore, our study contributes towards capturing the value of forest resources through the utilisation of native essential oils in South Korea.

1. Introduction

There is a large and sustainable supply of foliage, twigs, bark, and wood residue, and there are notable value-adding opportunities for unattended forest waste [1]. Essential oils extracted from forestry biomass waste are valuable owing to their bioactive compounds [2]. However, a considerable amount of valuable biomass resources after forest management are still underutilised. This is still the case today in South Korea.
The purpose of our previous study was to screen potential commercial essential oils from forestry resources in South Korea. Specifically, we reviewed prospective candidates for native essential oils from the Essential Oils Bank, which was established by the National Institute of Forest Science (NiFoS) in terms of both forest management and conservation. From a total of 39 listed candidates from forest resources, Pinaceae (L. kaempferi, P. densiflora, and P. koraiensis) and Cupressaceae (C. obtusa and C. pisifera) could be potential candidates for producing commercial essential oils, as their waste materials are easily obtained from plantations after forest management [3]. In this study, we focus on the development of the selected native essential oils (Pinaceae and Cupressaceae) from the previous study by exploring further information about their biological activities and potential uses.
The market for medicinal and aromatic plants is continuously growing, owing to the demand for their bioactive compounds and diverse uses [4]. Considering this situation, the high and increasing market value of essential oils could allow for the exploitation of forest resources to be economically viable [5]. Some studies have already been conducted to establish their better utilisation by converting under-valued waste resources. Specifically, essential oils and hydrolate (Cupressus lusitanica and Cistus ladanifer) from biomass wastes showed strong anti-inflammatory properties [2]. Hence, increasing the applications and markets for essential oils could bring new opportunities for the cost-effective, profitable, and sustainable management of unused forestry biomass. However, better knowledge of the biological activities and various applications of targeted essential oils is necessary for the development of essential oils from forest waste in South Korea. Therefore, this is a comprehensive review suggesting that forest waste could be utilised as a source of essential oils from the perspective of recently reported work in this field, together with the current status of the forestry and essential oils industry in South Korea. Specifically, we review the targeted essential oils, paying particular attention to their bioactive compounds and various applications.

2. Essential Oils Industry in South Korea

At present, there is a growing interest in essential oils, owing to their bioactive compounds together with their pleasant fragrance. Djilani and Dicko [6] explained that approximately 300 essential oils have been produced from at least 2000 plant species, out of which 300 are essential commercial crops. Table 1 shows the quantities of major commercial essential oils produced worldwide.
In South Korea, the domestic essential oil market heavily relies on imports from overseas. According to the trade statistics provided by the Korea Customs Service, the trade in essential oils and resionoids (H.S. code: 33) has resulted in a trade deficit (Table 2). There are several reasons for this.
First, the level of industrial essential oil technology remains at a fairly basic level by processing just the formulation and dilution. Although there are a variety of native aromatic crops in South Korea, it is still challenging to develop high-quality essential oils or fragrance products at the industrial level, owing to a lack of professional skill and expertise [9,10]. Second, the cultivation area and production volume of aromatic and medicinal crops are very limited in South Korea. So, there would be low price competitiveness compared to foreign products in the global market. Third, most studies of native aromatic and medicinal plants focused on the investigation of biological activities for developing herbal medicine from plant extract [11]. On the other hand, there is limited research on the development of native essential oils, including but not limited to production, extraction, and standardisation. The current study simply focused on the identification of chemical components and biological activities in oils. [12,13]. Due to these reasons, it is problematic to develop the commercial essential oil industry in South Korea. However, it is indispensable to discover and develop commercial essential oils from native plants in South Korea in response to Nagoya’s protocol.

3. Investigating the Selected Pinaceae and Cupressaceae for Essential Oils

Essential oils are highly volatile in the air, and their fragrances vary depending on plant material and species [14]. Specifically, the essential oils are obtained from flowers, buds, seeds, leaves, bark, fruits, and roots [15]. Yet, there is limited information on the chemical profile and scent descriptions of essential oils extracted from various parts. Based on the Essential Oils Bank, which was established by the National Institute of Forest Sciences (NiFoS), the fragrance information of Pinaceae and Cupressaceae was only focused on the essential oils extracted from leaves.
We focus on screening the Pinaceae and Cupressaceae essential oils from various parts from the perspective of their bioactive compounds and various applications. However, the chemical profile can be variable, even within the same species. Specifically, the variation in the chemical components of essential oils can be caused by genetic and environmental factors [16]. Furthermore, biological activity can be highly variable in terms of bioactive components in oils. Hence, this section is written with the purpose of giving an overview of current knowledge about the chemical profile and biological activity of targeted essential oils so as to find research areas that can facilitate the applications of essential oils in various industries.

3.1. Pinaceae Essential Oils

3.1.1. L. kaempferi

L. kaempferi is one of the main coniferous species in South Korea, so it is a major contributor to the national forest stock [17,18]. Because of this, most studies have been focused on the optimisation of plantations for efficient forest management [19,20,21], and there are limited studies on the extract and essential oils from L. kaempferi. The overall information on the essential oils extracted from the leaves and wood is summarised in Table 3. The essential oils from the leaves demonstrated herbicidal activity. According to the greenhouse experiment, treated plants by foliar application of 10% essential oils showed a burndown effect on their leaves [22]. Furthermore, Kim et al. [23] found that L. kaempferi essential oils from leaves showed an anti-dermatophyte effect, owing to the active antifungal components, such as terpinene-4-ol, α-terpineol, and α-cadinol. Lastly, the essential oils extracted from wood could be used as an anti-inflammatory agent [24].

3.1.2. P. densiflora

P. densiflora has been used in folk medicine for a long time in South Korea. Pine needles have been widely used as food ingredients, food additives, and folk medicines in pine-based products due to their characteristic aroma, taste, and health [25,26]. For example, the leaves of P. densiflora have been used to prepare drinks as tea, and pine needles have been used in folk medicines for liver diseases, skin diseases, and hypertension [27,28,29]. Currently, P. densiflora extract is being included in cosmetic and functional foods and sold in the local market in South Korea. As shown in Table 4, the essential oils are extracted from the leaves, wood, and twigs of P. densiflora. Furthermore, their major chemical components, biological activities, and potential uses of essential oils extracted from various parts are listed, respectively. Sangwan et al. [16] mentioned that the chemical profile can vary depending on the specific part used from the same plant. The P. densiflora essential oils’ chemical components in leaves and twigs are similar. However, the component α-pinene is the most abundant in leaf essential oils, while β-pinene is predominantly found in the essential oils extracted from twigs [30]. Unlike essential oils from the leaves and twigs of P. densiflora, the major chemical component of wood essential oils is longifolene (14.3%) [24].
P. densiflora essential oils extracted from various parts show diverse biological activities. P. densiflora leaf essential oils showed antioxidant and anti-ageing activity owing to phellandrene and B-pinene. So, it could be used as a functional cosmetic ingredient for anti-wrinkle benefits [30]. Furthermore, essential oils contain anti-proliferative, anti-survival, and pro-apoptotic effects on human oral squamous cells because of α-pinene, leading to the cytotoxic effect [31]. Hence, it could have potential usefulness in cancer prevention. Lastly, essential oils show strong antibacterial activities [32]. The essential oils can be used as natural antimicrobial and antibacterial substances in the food industry and the household cleaning product industry. The essential oils from wood contained the chemical components of α-pinene (47.2%), longifolene (14.3%), and β-phellandrene (11.8%). The essential oils with bioactive compounds such as β-pinene and longifolene showed an anti-inflammatory effect by inhibiting the degranulation and expression of cytokines [24]. Hence, it could be conducive to relieving allergic inflammation, which can be used for pharmaceutical purposes. Lastly, essential oils from twigs of P. densiflora also showed antioxidant and anti-ageing activities in terms of similar chemical constituents in essential oils extracted from leaves [30].
Table 4. The major constituents, biological activities, and potential application of essential oils extracted from P. densiflora.
Table 4. The major constituents, biological activities, and potential application of essential oils extracted from P. densiflora.
Scientific NamesPlant PartsMajor Chemical ProfileBiological ActivitiesApplicationRef.
P. densifloraleavesα-pinene (21.6%)
limonene (13.1%)
caryophellene
(11.4%)
[30]
antioxidant
and anti-ageing activities
cosmetic industry[30]
anti-cancerpharmaceutical industry[31]
antibacterial food industry[32]
woodα-pinene (47.2%)
longifolene (14.3%)
β-phellandrene (11.8%)
anti-inflammatory effectpharmaceutical industry[24]
twigsβ-pinene (22.4%)
α-pinene (17.3%)
limonene (15%)
[30]
antioxidant and anti-ageing activitiescosmetic industry[30]

3.1.3. P. koraiensis

P. koraiensis, commonly called Korean nut pine, has been used as a food supplement and in traditional Asian medicine for the longest time [33]. According to Table 5, P. koraiensis essential oils are extracted from seed, wood, cones, and leaves. The major constituents of EO obtained from the seed and cone are α-pinene (29.9%), D-limonene (19.3%), and Β-pinene (11.2%). The essential oils showed mild antimicrobial properties by inhibiting the growth of other pathogens related to acne. Therefore, it can be used as a natural cosmetic ingredient or as an antimicrobial substance [14].
The essential oils from wood showed an anti-inflammatory effect. In particular, the chemical components of Β-pinene and α-terpineol in oils were assumed to be the most contributing bioactive compounds to the anti-inflammatory activity [34].
Essential oils extracted from cones promoted anti-metastatic activity in breast cancer cells by inhibiting tumour necrosis through the action of bioactive compounds [35]. Moreover, the cone essential oils showed significant antimicrobial activities, especially against pathogenic fungal strains such as Candida glabrata YFCC 062 and Cryptococcus neoformans B 42419. Therefore, the results indicate that the essential oils from the cones can be used in various ways as a non-toxic and environmentally friendly disinfectant [36].
Essential oils extracted from leaves show a variety of biological activities, and they can be used in various manners. First, essential oils extracted from leaves showed anti-cancer activity via the inhibition of PAK1 expression, suggesting they might be a potent chemotherapeutic agent for colorectal cancer [37]. Second, they showed the anti-diabetic effect in mice with streptozotocin (STZ)-induced type 1 diabetes and on HIT-T15 pancreatic B cells, employing the hypoglycaemic potential effects [38]. Therefore, it can be a good candidate for natural anti-diabetic materials. For example, hypoglycaemic herbal medicines could be used for long-term diabetes patients with less toxicity [39,40]. Furthermore, the essential oils from the leaves showed antifungal activity against Candida albicans [41]. Lastly, P. koraiensis essential oils have effective deodorisation and inhibitory activity against the oral cavity in this study and might be potential material in the oral sanitary industry [42].
Table 5. The major constituents, biological activities, and potential application of essential oils extracted from P. koraiensis.
Table 5. The major constituents, biological activities, and potential application of essential oils extracted from P. koraiensis.
Scientific NamesPlant PartsMajor Chemical ProfileBiological ActivitiesApplicationRef.
P. koraiensisseed and coneα-pinene (29.9%)
D-limonene (19.3%)
Β-pinene (11.2%)
[14]
anti-microbial activity (acne)cosmetic industry[14]
woodα-pinene (27.0%)
Β-pinene
(11.2%)
α-terpineol
(7.1%)
anti-inflammatory effectpharmaceutical industry[34]
conesD-limonene (28.0%),
α-pinene (23.9%),
Β-pinene (12.1%)
[41]
anti-cancerpharmaceutical industry[35]
anti-microbial activitysanitary industry (disinfectant)[36]
leavesα-pinene
(10.5%)
myrcene
(7.3%)
bornyl acetate
(7.2%)
[41]
anti-cancer
(colorectal cancer)
pharmaceutical industry[37]
anti-diabetic effectpharmaceutical and[38]
antifungal effectfood industry[41]
anti-oral microbial activity and deodorisation effectsanitary industry (dental)[42]

3.2. Cupressaceae Essential Oils

3.2.1. C. obtusa Oil

C. obtusa has been widely used for various household purposes in South Korea. In general, C. obtusa has been used to make furniture owing to the high quality of the timber [43]. Also, the oil extracted from the branches, leaves, and twigs of C. obtusa has been commercially used as a functional additive in the production of soap, toothpaste, and cosmetics owing to its unique fragrance and bioactive compounds [44]. Furthermore, inhalation with the essential oils of C. obtusa is known as forest bathing or aromatherapy [45].
As shown in Table 6, C. obtusa essential oils are extracted from leaves, wood (sawdust), and fruit. The major chemical components of oils differ depending on the plant part from which they are extracted. In particular, essential oils from the leaves have been widely studied for several biological activities. First, C. obtusa essential oils showed an antibacterial effect by inhibiting the growth of various microorganisms. Specifically, essential oils were found to be effective in inhibiting the growth of various airborne microorganisms in indoor spaces [46]. Musee et al. [47] emphasised that disinfectants should not only be effective in reducing the microbes present in the air but also not be toxic to humans. Also, essential oils showed a deodorisation effect by mitigating an offensive odour [48]. Therefore, essential oils could be used as safe natural disinfectants and deodorants in the household cleaning industry. Second, C. obtusa oil has potential as a functional cosmetic ingredient. It can be utilised in anti-ageing targeted products for wrinkles, skin-barrier, and moisturising effects [49] and supplemental products for improving atopic dermatitis [50]. Third, C. obtusa oil could be a novel source of inflammation-specific pharmacological drugs, especially for peripheral pain. Based on in vivo experiments (mice), the inflammatory effect of C. obtusa oils was elucidated [51,52]. Yet, further research is needed to investigate the specific mechanisms and potential side effects of C. obtusa essential oils [51]. Fourth, essential oils with bioactive compounds showed insecticidal activity. Owing to bornyl acetate and terpinyl acetate, essential oils showed insecticidal activity, implying their potential use as strong insecticides [53]. Park et al. [54] found that essential oils could be useful in food and agriculture by managing the populations of rice weevils. Also, it can be potentially used as a ‘human-friendly’ insect repellent [55]. Lastly, C. obtusa oils might promote hair growth in an animal model and show a positive regulator of hair growth, owing to the bioactive components cuminol, eucarvone, and calamenene [56]. Additionally, the essential oil extracted from the pruned leaves and twigs showed both anti-cariogenic and anti-inflammatory effects. Specifically, C. obtusa essential oil inhibited the decrease in pH induced by Streptococcus. mutans, thereby inhibiting dental caries [57].
Currently, research on C. obtusa essential oils from sawdust and fruit is lacking. By recycling wood waste, it can be transformed into commercially valuable products, such as essential oils [58]. The major constituents of C. obtusa essential oils from sawdust are juniper camphor (12.5%), fonenol (12.4%), and d-9-capnellene-3-b-ol-8-one (10.1%). It showed high antioxidant activity; therefore, it could be a natural antioxidant in food by stabilising food against oxidative deterioration [59]. The major essential oils from the fruit of C. obtusa include B-caryophyllene (23.7%), myrcene (8.1%), and p-cymene (7.6%) [60]. Yet, there has been no research on the identified biological activity and potential application of essential oils from fruit.
Table 6. The major constituents, biological activities, and potential application of essential oils extracted from C. obtusa.
Table 6. The major constituents, biological activities, and potential application of essential oils extracted from C. obtusa.
Scientific NamesPlant PartsMajor Chemical ProfileBiological ActivitiesApplicationRef.
C. obtusaleavesα-terpinyl acetate (13.7%)
sabinene (11.0%)
isobornyl acetate (8.9%)
[61]
antibacterial and antimicrobial effecthousehold cleaning industry (disinfectant and deodorant)[46,48,62]
anti-ageing effectcosmetic industry[49]
relieving the allergy
(atopic dermatitis)
[50]
anti-inflammatory effectpharmaceutical industry[51]
anti-nociceptive and anti-inflammatory effects[52]
insecticidal activitiesagriculture and food industry [54,55]
hair growthfunctional cosmetic industry[56]
leaves and twigα-terpinene (40.6%)
bornyl acetate (12.5%)
α-pinene (11.4%)
[57]
anti-cariogenic effectpharmaceutical industry[57]
saw-dustjuniper camphor (12.5%)
fonenol (12.4%)
d-9-capnellene-3-b-ol-8-one (10.1%)
antioxidant activityfood industry[59]
fruitB-caryophyllene (23.7%)
myrcene (8.1%)
p-cymene (7.6%)
[60]
---

3.2.2. C. pisifera Oil

Among the other selected essential oils, very little work has been done on the study of C. pisifera essential oils. The major components in C. pisifera essential oils extracted from leaves are 3-carene (35.0%), (−)-bornyl acetate (19.8%), and α-pinene (13.0%) [63] (Table 7). The C. pisifera essential oil showed strong insecticidal activity [64]. However, little work has been done on the essential oils extracted from the fruit. Hong et al. [60] studied the chemical profile of C. pisifera essential oils extracted from fruit. The major chemical components are (−)-3-carene (30.3%), α-pinene (29.4%), and myrcene (15.1%).

4. Utilising the Forest Waste after Forest Management for Essential Oils

Due to climate change, many countries have declared themselves Net-Zero countries, including South Korea. For example, in 2018, the National Institute of Forest Science (NiFoS) was established to promote an efficient utilisation system for forest resources in renewable energy supply through the use of forest biomass waste.
Since 1972, South Korea has conducted a periodic National Forest Inventory (NFI) to manage forest resources efficiently and provide fundamental public data for forest policy. There is an increasing demand for public data and statistics to assess the economic and social value of forests, such as greenhouse gas absorption and the maintenance and enhancement of biodiversity. The NFI is a 5-year periodic monitoring system, and the report consists of five sections, including statistics on forest area, timber volume, timber resources (number of trees, stand volume, large-sized timber, and quality grade), biomass, carbon storage, and greenhouse gas absorption in the forest sector [65].
According to Table 8, the selected species could ensure a constant supply from forest management. However, the cost of transportation of forest biomass from forest management would need to be considered. Cambero and Sowlati [66] emphasised that the viability and feasibility of utilising the forest biomass would depend on ensuring the long-term availability of biomass supply with the required quality at a competitive cost. Forest residues after forest management are scattered over wide regions, so the extra cost of collection, handling, and transportation would also need to be considered [67]. Essential oil production from wild trees depends essentially on the abundance of the species and the costs of harvesting. Yet, oil production from the cultivated species includes considerable investments in the plantations [68]. Essential oils from wild sources are generally commercialised in low volume and at high prices, which can ensure a profitable industry. Hence, developing an essential oil industry from forest biomass needs to be a cost-efficient part of the forest biomass supply chain.
Unused forest waste includes diseased trees caused by pine wilt disease in South Korea. The stressed or diseased plant material can develop larger amounts of volatiles, and undesirable chemical compounds can create an allergic response. Figueiredo et al. [68] explained that stressed or diseased plant material induces increased amounts of volatiles, and undesirable chemical compounds can create an allergic response. The relationship between oil content and damage could be related to oil composition rather than oil yield, and this could differ within as well as between species. Therefore, further research is needed to identify the chemical profile of targeted essential oils extracted from unused forest biomass for safety efficacy. In conclusion, recycling and reuse of these renewable resources strengthen industries and technology to evolve in more sustainable ways and create more opportunities for the forest industry [69].

5. Safety of Essential Oils

Owing to their bioactive compounds and pleasant fragrance, essential oils have been used in various industries in recent times. Essential oils contain natural constituents, leading consumers to consider essential oils safe and nontoxic. Yet, the use of essential oils may still be hazardous for humans. For example, α-pinene is considered one of the allergenic chemical components in tea tree oil (Melaleuca alternifolia Cheel.), which is used all around the world [70]. In general, possible adverse effects of essential oils include nausea, vomiting, necrosis, mucous membranes, and skin irritation [71].
According to the European Union (EU) Cosmetics Regulation, 18 chemical components in essential oils contain potential allergen substances [72]. In particular, the most frequently encountered chemical components in oils are citral, citronellol, eugenol, farnesol, geraniol, limonene, and linalool. For safety reasons, the provider must be declared on the packaging or in the information description if the concentration of these allergenic fragrances is higher than the permissible concentration in the product [73].
The screened essential oils in this current study contained allergenic chemical components, such as limonene and D-limonene (Table 9). Both chemical components are widely used as fragrance and flavouring agents in cosmetic products, pharmaceuticals, perfumes, and food. As shown in Table 9, P. densiflora essential oil contains the allergenic chemical component limonene. When exposed to air, it can be easily oxidised to carvone, carveol, and limonene oxide. Altered chemical components can cause skin irritation and dermal sensitisation [72]. Several studies have reported that the oxidation products of limonene can cause allergic contact dermatitis [74,75]. The major component of P. koraiensis essential oil extracted from seed and cone is D-limonene. It is an irritant in high concentration, and its oxidation products, such as limonene oxide and limonene hydroperoxides, are allergenic, too [76,77]. For example, Roman chamomile (Anthemis nobilis) might show an allergic reaction owing to D-limonene [78]. Therefore, a more careful approach is needed when developing P. densiflora and P. koraiensis essential oils for use in cosmetics and pharmaceuticals, with respect to their suitability for tracking the chemical alternations in oils. Moreover, it is also necessary to develop reproducible and reliable analytical methods for assessing both pure and altered essential oils as part of quality control.
Chemical components in oils are known to easily covert into each other by oxidation, isomerisation, cyclisation, or dehydrogenation reactions, triggered either enzymatically or chemically [79]. The oxidation of essential oils would increase their allergenic potency. Rudbäck et al. [80] found that α-terpinene undergoes rapid autoxidation upon air exposure, and oxidation products can induce the contact allergy. Specifically, the sensitisation potency of autoxidised α-terpinene was nearly nine times higher compared to that of pure α-terpinene. Hence, it is important to use essential oils safely and carefully to minimise the potential adverse risks associated with the problematic and undesirable chemical constituents. Furthermore, it might be advisable for the industry to provide recommendable storage conditions and use-by dates for essential oils to ensure their stability and safety.

6. Limitations and Prospects

The shortage of landfill space, greenhouse gas emissions, and residue runoff have spurred efforts to find alternative ways for traditional waste management [5]. For example, new composites utilising organic waste and residues from agricultural and industrial processes have been developed [81]. Likewise, there is a case study to assess the opportunities, constraints, and information required to integrate the recovery of essential oils into forest and mill operations, as might be used in northern Arizona. Northern Arizona’s forest is composed of ponderosa pine (Pinus ponderosa), which produces timber, essential oils, and resins. The study confirmed the potential output with a programme of forest thinning and biomass utilisation [82]. In another case, there are several plant species (Pinus pinaster, Eucalyptus globulus, Cistus ladanifer, and Lavandula sp.) in the Algarve region (southern Portugal), which contribute to a significant amount of residual biomass after forest management. Lastly, there was collaborative governance in Eucalyptus oil industry development in forest areas in Indonesia. The study emphasised building a shared vision among the actors involved as a reference for success in the development of the Eucalyptus oil industry in the future. This would be available to achieve productive and sustainable forest management through collaboration among the government and the essential oil industry [83].
There is no current pilot-scale study for the targeted essential oil crops in South Korea, including but not limited to oil yield, chemical constituents, safety efficacy, and biological activity. However, the global essential oil market requires consistent, high-quality products with reliability of supply at competitive prices. This pilot-scale study would be crucial in evaluating the business potential for the development of the native essential oil industry in South Korea. Therefore, processing the pilot-scale study for the development of native essential oils is urgently needed. According to a pilot-scale study, essential oil yields were lower than those performed on a laboratory scale and reported in the literature. Furthermore, it is recommended to use industrial equipment for the production of essential oils. Processing at an industrial scale would allow optimisation of the operating conditions for commercial essential oil production [5]. Moreover, qualifying the International Organisation for Standardisation (ISO) would strengthen the market competitiveness of the essential oils domestically as well as internationally. For example, the chemical profile of tea tree oil (Melaleuca alternifolia) has been regulated by the ISO entitled “Oil of Melaleuca terpinen-4-ol type (tea tree oil)” (ISO-4730) and specifies the chemical compositional limit for the 14 constituents [84]. ISO standardised many analytical methods for controlling the quality of chemical components in oils, thus focusing on the quality control of essential oils in the global market [85].
To develop commercial native essential oils from forest waste in South Korea, it will be necessary to process further research under the pilot study levels below. Firstly, the mentioned potential candidates will require extraction of the oils and then confirmation of oil yield and chemical constituents. After that, the identified chemical constituents in oils would be able to investigate the various biological activities. It would be conducive to utilising essential oils based on identified bioactive constituents in oils. There are numerous studies on the biological activities of essential oils, elucidating their mechanisms [86]. In particular, studies on antimicrobial, antioxidant, anti-inflammatory, and anti-cancer activities have been investigated in many cell and animal models. However, very little work has been carried out on human clinical studies as phytotherapeutic agents, but the anticancer activity of essential oils should take a careful approach to the development of phytotherapeutic agents. Essential oils and aromatherapy are considered complementary therapies at this stage. Therefore, clinical studies are needed to investigate the real efficacy and safety of essential oils [87].

7. Conclusions

Unused forest biomass, a valuable renewable resource, has opportunities for sustainable energy production and other potential applications. Owing to the lack of professional skill and expertise, it will be challenging to develop a commercial essential oil industry in South Korea. However, there are clear imperatives to discover and develop essential oils from native plants in South Korea in response to Nagoya’s protocol.
A precedent study on the development of native essential oils from forestry resources suggested Pinaceae and Cupressaceae could be potential candidates for essential oils in terms of forest management and conservation in South Korea. By deepening the previous study, we reviewed the Pinaceae (L. kaempferi, P. densiflora, and P. koraiensis) and Cupressaceae (C. obtusa and C. pisifera) essential oils extracted from various parts from the perspective of their bioactive compounds and potential applications. The current study, along with the previous study, has confirmed the possibility of the idea that unused forest biomass may potentially be an untapped valuable source of essential oils. However, it is important to set up a cost-efficient system for the forest biomass supply chain.
By addressing the challenges and embracing the opportunities, Pinaceae and Cupressaceae essential oils extracted from various parts showed diverse biological activities. Therefore, essential oils of Pinaceae and Cupressaceae extracted from unused forest biomass could be used in various ways as non-toxic and environmentally friendly products.

Author Contributions

C.P. (conceptualisation, investigation, writing—original draft, and writing—review and editing); H.W. (conceptualisation and review and editing); M.-J.P. (conceptualization and review and editing). All authors have read and agreed to the published version of the manuscript.

Funding

This research was carried out with the support of the R&D programme for Forest Science Technology (project No. 2019151B10-2323-0301) provided by the Korea Forest Service.

Data Availability Statement

Not applicable.

Acknowledgments

This paper and the concept behind it would not have been possible without the valuable work of the Essential Oils Bank, which was established by the National Institute of Forest Science (NiFoS).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Thorenz, A.; Wietschel, L.; Stindt, D.; Tuma, A. Assessment of agroforestry residue potentials for the bioeconomy in the European Union. J. Clean. Prod. 2018, 176, 348–359. [Google Scholar] [CrossRef] [PubMed]
  2. Tavares, C.S.; Martins, A.; Faleiro, M.L.; Miguel, M.G.; Duarte, L.C.; Gameiro, J.A.; Roseiro, L.B.; Figueiredo, A.C. Bioproducts from forest biomass: Essential oils and hydrolates from wastes of Cupressus lusitanica Mill. and Cistus ladanifer L. Ind. Crops Prod. 2020, 144, 112034. [Google Scholar] [CrossRef]
  3. Park, C.; Woo, H. Development of Native Essential Oils from Forestry Resources in South Korea. Life 2022, 12, 1995. [Google Scholar] [CrossRef] [PubMed]
  4. Lubbe, A.; Verpoorte, R. Cultivation of medicinal and aromatic plants for specialty industrial materials. Ind. Crops Prod. 2011, 34, 785–801. [Google Scholar] [CrossRef]
  5. Mediavilla, I.; Guillamón, E.; Ruiz, A.; Esteban, L.S. Essential oils from residual foliage of forest tree and shrub species: Yield and antioxidant capacity. Molecules 2021, 26, 3257. [Google Scholar] [CrossRef] [PubMed]
  6. Djilani, A.; Dicko, A. The therapeutic benefits of essential oils. In Nutrition, Well-Being and Health; Intech: Houston, TX, USA, 2012; Volume 7, pp. 155–179. [Google Scholar]
  7. Lawrence, B.M. A preliminary report on the world production of some selected essential oils and countries. Perfum. Flavorist 2009, 34, 38–44. [Google Scholar]
  8. Korea Customs Service. Trade Statistics. Available online: https://unipass.customs.go.kr/ets/index_eng.do (accessed on 19 April 2023).
  9. Kim, M.; Sowndhararajan, K.; Kim, S. The chemical composition and biological activities of essential oil from Korean native thyme Bak-Ri-Hyang (Thymus quinquecostatus Celak.). Molecules 2022, 27, 4251. [Google Scholar] [CrossRef]
  10. Lee, H.J. Development of New Aromatic Materials Using Native Korean Aromatic Plants Targeting at Export. Available online: https://scienceon.kisti.re.kr/commons/util/originalView.do?cn=TRKO201400023981&dbt=TRKO&rn= (accessed on 19 April 2023).
  11. Kang, D.G.; Keun Yun, C.; Lee, H.S. Screening and comparison of antioxidant activity of solvent extracts of herbal medicines used in Korea. J. Ethnopharmacol. 2003, 87, 231–236. [Google Scholar] [CrossRef]
  12. Kim, M.; Moon, J.C.; Kim, S.; Sowndhararajan, K. Morphological, chemical, and genetic characteristics of Korean native thyme Bak-ri-hyang (Thymus quinquecostatus Celak.). Antibiotics 2020, 9, 289. [Google Scholar] [CrossRef]
  13. Lee, J.H.; Lee, B.K.; Kim, J.H.; Lee, S.H.; Hong, S.K. Comparison of chemical compositions and antimicrobial activities of essential oils from three conifer trees; Pinus densiflora, Cryptomeria japonica, and Chamaecyparis obtusa. J. Microbiol. Biotechnol. 2009, 19, 391–396. [Google Scholar] [CrossRef]
  14. Choi, J.W.; Kim, R. Antimicrobial Activity of Essential Oil of Pinus koraiensis Seed Against Pathogens Related to Acne. KSBB J. 2014, 29, 179–182. [Google Scholar] [CrossRef]
  15. Burt, S. Essential oils: Their antibacterial properties and potential applications in foods—A review. Int. J. Food Microbiol. 2004, 94, 223–253. [Google Scholar] [CrossRef] [PubMed]
  16. Sangwan, N.; Farooqi, A.; Shabih, F.; Sangwan, R. Regulation of essential oil production in plants. Plant Growth Regul. 2001, 34, 3–21. [Google Scholar] [CrossRef]
  17. Kang, T.; Son, Y.; Yim, J.; Jeon, J. Estimation of carbon stock and uptake for Larix kaempferi Lamb. J. Clim. Chang. 2016, 7, 499–506. [Google Scholar] [CrossRef]
  18. Lee, S.; Doyog, N.D.; Lee, Y.J. Comparative analysis of simple volume models for Japanese Larch (Larix kaempferi) species in the Central Region of South Korea. J. Agric. Life Sci. 2017, 51, 55–64. [Google Scholar] [CrossRef]
  19. Kim, M.; Lee, W.K.; Kim, Y.S.; Lim, C.H.; Song, C.; Park, T.; Son, Y.; Son, Y.M. Impact of thinning intensity on the diameter and height growth of Larix kaempferi stands in central Korea. For. Sci. Technol. 2016, 12, 77–87. [Google Scholar] [CrossRef]
  20. Seo, K.S.; Lee, B.; Yun, K.W. Chemical Composition and Antibacterial Activity of Essential Oils Extracted from Wild and Planted Thuja orientalis Leaves in Korea. J. Essent. Oil-Bear. Plants 2019, 22, 1407–1415. [Google Scholar] [CrossRef]
  21. Moon, M.Y.; Kim, S.S.; Lee, D.S.; Yang, H.M.; Park, C.W.; Kim, H.S.; Park, Y.S. Effects of forest management practices on moth communities in a Japanese larch (Larix kaempferi (Lamb.) Carrière) plantation. Forests 2018, 9, 574. [Google Scholar] [CrossRef]
  22. Yun, M.S.; Cho, H.M.; Yeon, B.R.; Choi, J.S.; Kim, S. Herbicidal activities of essential oils from pine, nut pine, larch and khingan fir in Korea. Weed Turfgrass Sci. 2013, 2, 30–37. [Google Scholar] [CrossRef]
  23. Kim, S.; Lee, S.; Hong, C.; Jang, S.; Lee, S.; Park, M.; Choi, I. Evaluation on anti-dermatophyte effect of Larix (kaempferi) essential oil on the morphological changes of eermatophyte fungal Hyphae. J. Korean Wood Sci. Technol. 2013, 41, 247–257. [Google Scholar] [CrossRef]
  24. Yang, J.; Choi, W.S.; Kim, J.W.; Lee, S.S.; Park, M.J. Anti-inflammatory effect of essential oils extracted from wood of four coniferous tree species. J. Korean Wood Sci. Technol. 2019, 47, 674–691. [Google Scholar] [CrossRef]
  25. Lee, J.G.; Lee, C.G.; Kwag, J.J.; Buglass, A.J.; Lee, G.H. Determination of optimum conditions for the analysis of volatile components in pine needles by double-shot pyrolysis–gas chromatography–mass spectrometry. J. Chromatogr. A 2005, 1089, 227–234. [Google Scholar] [CrossRef]
  26. Kwak, C.S.; Moon, S.C.; Lee, M.S. Antioxidant, antimutagenic, and antitumor effects of pine needles (Pinus densiflora). Nutr. Cancer 2006, 56, 162–171. [Google Scholar] [CrossRef] [PubMed]
  27. Lee, E. Effects of powdered pine needle (Pinus densiflora seib et Zucc.) on serum and liver lipid composition and antioxidative capacity in rats fed high oxidized fat. J. Korean Soc. Food Sci. Nutr. 2003, 32, 926–930. [Google Scholar]
  28. Kang, Y.; Park, Y.; Ha, T.; Moon, K. Effects of pine needle extracts on serum and liver lipid contents in rats fed high fat diet. J. Korean Soc. Food Sci. Nutr. 1996, 25, 367–373. [Google Scholar]
  29. Kim, K.Y.; Chung, H.J. Flavor compounds of pine sprout tea and pine needle tea. J. Agric. Food Chem. 2000, 48, 1269–1272. [Google Scholar] [CrossRef]
  30. Kim, Y.J.; Cho, B.J.; Ko, M.S.; Jung, J.M.; Kim, H.R.; Song, H.S.; Lee, J.Y.; Sim, S.S.; Kim, C.J. Anti-oxidant and anti-aging activities of essential oils of Pinus densiflora needles and twigs. Yakhak Hoeji 2010, 54, 215–225. [Google Scholar]
  31. Jo, J.R.; Park, J.S.; Park, Y.K.; Chae, Y.Z.; Lee, G.H.; Park, G.Y.; Jang, B.C. Pinus densiflora leaf essential oil induces apoptosis via ROS generation and activation of caspases in YD-8 human oral cancer cells. Int. J. Oncol. 2012, 40, 1238–1245. [Google Scholar] [CrossRef]
  32. Park, J.S.; Lee, G.H. Volatile compounds and antimicrobial and antioxidant activities of the essential oils of the needles of Pinus densiflora and Pinus thunbergii. J. Sci. Food Agric. 2011, 91, 703–709. [Google Scholar] [CrossRef]
  33. Yang, J.; Choi, W.S.; Jeung, E.B.; Kim, K.J.; Park, M.J. Anti-inflammatory effect of essential oil extracted from Pinus densiflora (Sieb. et Zucc.) wood on RBL-2H3 cells. J. Wood Sci. 2021, 67, 52. [Google Scholar] [CrossRef]
  34. Yang, J.; Choi, W.S.; Kim, K.J.; Eom, C.D.; Park, M.J. Investigation of active anti-inflammatory constituents of essential oil from Pinus koraiensis (Sieb. et Zucc.) wood in LPS-stimulated RBL-2H3 cells. Biomolecules 2021, 11, 817. [Google Scholar] [CrossRef] [PubMed]
  35. Lee, J.H.; Lee, K.; Lee, D.H.; Shin, S.Y.; Yong, Y.; Lee, Y.H. Anti-invasive effect of β-myrcene, a component of the essential oil from Pinus koraiensis cones, in metastatic MDA-MB-231 human breast cancer cells. J. Korean Soc. Appl. Biol. Chem. 2015, 58, 563–569. [Google Scholar] [CrossRef]
  36. Lee, J.H.; Yang, H.Y.; Lee, H.S.; Hong, S.K. Chemical composition and antimicrobial activity of essential oil from cones of Pinus koraiensis. J. Microbiol. Biotechnol. 2008, 18, 497–502. [Google Scholar]
  37. Cho, S.M.; Lee, E.O.; Kim, S.H.; Lee, H.J. Essential oil of Pinus koraiensis inhibits cell proliferation and migration via inhibition of p21-activated kinase 1 pathway in HCT116 colorectal cancer cells. BMC Complement. Altern. Med. 2014, 14, 275. [Google Scholar] [CrossRef] [PubMed]
  38. Joo, H.E.; Lee, H.J.; Sohn, E.J.; Lee, M.H.; Ko, H.S.; Jeong, S.J.; Lee, H.J.; Kim, S.H. Anti-diabetic potential of the essential oil of Pinus koraiensis leaves toward streptozotocin-treated mice and HIT-T15 pancreatic β cells. Biosci. Biotechnol. Biochem. 2013, 77, 1997–2001. [Google Scholar] [CrossRef]
  39. Boukhris, M.; Bouaziz, M.; Feki, I.; Jemai, H.; El Feki, A.; Sayadi, S. Hypoglycemic and antioxidant effects of leaf essential oil of Pelargonium graveolens L’Hér. in alloxan induced diabetic rats. Lipids Health Dis. 2012, 11, 81. [Google Scholar] [CrossRef]
  40. Sriramavaratharajan, V.; Murugan, R. Chemical profile of leaf essential oil of Cinnamomum walaiwarense and comparison of its antioxidant and hypoglycemic activities with the major constituent benzyl benzoate. Nat. Prod. Commun. 2018, 13, 779–782. [Google Scholar] [CrossRef]
  41. Hong, E.J.; Na, K.J.; Choi, I.G.; Choi, K.C.; Jeung, E.B. Antibacterial and antifungal effects of essential oils from coniferous trees. Biol. Pharm. Bull. 2004, 27, 863–866. [Google Scholar] [CrossRef]
  42. Hwang, H.J.; Yu, J.S.; Lee, H.Y.; Kwon, D.J.; Han, W.; Heo, S.I.; Kim, S.Y. Evaluations on deodorization effect and anti-oral microbial activity of essential oil from Pinus koraiensis. Korean J. Plant Res. 2014, 27, 1–10. [Google Scholar] [CrossRef]
  43. Joung, Y.W.; Kim, Y.m.; Jang, Y.A. Studies on the antioxidant and whitening effects of Chamaecyparis obtusa extract. J. Korean Appl. Sci. Technol. 2020, 37, 1496–1506. [Google Scholar]
  44. Ahn, J.Y.; Lee, S.S.; Kang, H.Y. Biological activities of essential oil from Chamaecyparis obtusa. J. Soc. Cosmet. Sci. Korea 2004, 30, 503–507. [Google Scholar]
  45. Bae, D.; Seol, H.; Yoon, H.G.; Na, J.R.; Oh, K.; Choi, C.Y.; Lee, D.w.; Jun, W.; Youl Lee, K.; Lee, J. Inhaled essential oil from Chamaecyparis obtuse ameliorates the impairments of cognitive function induced by injection of β-amyloid in rats. Pharm. Biol. 2012, 50, 900–910. [Google Scholar] [CrossRef]
  46. Song, S.Y.; Park, D.H.; Lee, S.H.; Choi, C.Y.; Shim, J.H.; Yoon, G.; Park, J.W.; Bae, M.S.; Cho, S.S. Indoor Space Disinfection Effect and Bioactive Components of Chamaecyparis obtusa Essential Oil. Processes 2023, 11, 1446. [Google Scholar] [CrossRef]
  47. Musee, N.; Ngwenya, P.; Motaung, L.K.; Moshuhla, K.; Nomngongo, P. Occurrence, effects, and ecological risks of chemicals in sanitizers and disinfectants: A review. Environ. Chem. Ecotoxicol. 2023, 5, 62–78. [Google Scholar] [CrossRef]
  48. Kim, H.; Han, S.; Mang, J. Evaluations on the deodorization effect and antibacterial activity of Chamaecyparis obtusa essential oil. Korean J. Odor Res. Eng. 2009, 8, 111–117. [Google Scholar]
  49. Kang, E.J.; Jang, Y.A.; Lee, J.T.; Kim, S.H.; Kim, S.; Bak, J.; Choi, Y.S. The effects of Chamaecyparis obtusa oil on anti-wrinkle, skin-barrier and moisturizing. J. Korean Appl. Sci. Technol. 2023, 40, 309–321. [Google Scholar] [CrossRef]
  50. Lim, G.S.; Kim, R.; Cho, H.; Moon, Y.S.; Choi, C.N. Comparison of volatile compounds of Chamaecyparis obtusa essential oil and its application on the improvement of atopic dermatitis. Korean Soc. Biotehcnol. Bioeng. J. 2013, 28, 115–122. [Google Scholar] [CrossRef]
  51. An, B.S.; Kang, J.H.; Yang, H.; Jung, E.M.; Kang, H.S.; Choi, I.G.; Park, M.-J.; Jeung, E.B. Anti-inflammatory effects of essential oils from Chamaecyparis obtusa via the cyclooxygenase-2 pathway in rats. Mol. Med. Rep. 2013, 8, 255–259. [Google Scholar] [CrossRef]
  52. Park, Y.; Jung, S.M.; Yoo, S.A.; Kim, W.U.; Cho, C.S.; Park, B.J.; Woo, J.M.; Yoon, C.H. Antinociceptive and anti-inflammatory effects of essential oil extracted from Chamaecyparis obtusa in mice. Int. Immunopharmacol. 2015, 29, 320–325. [Google Scholar] [CrossRef] [PubMed]
  53. Xie, Y.; Wang, K.; Huang, Q.; Lei, C. Evaluation toxicity of monoterpenes to subterranean termite, Reticulitermes chinensis Snyder. Ind. Crops Prod. 2014, 53, 163–166. [Google Scholar] [CrossRef]
  54. Park, I.K.; Lee, S.G.; Choi, D.H.; Park, J.D.; Ahn, Y.J. Insecticidal activities of constituents identified in the essential oil from leaves of Chamaecyparis obtusa against Callosobruchus chinensis (L.) and Sitophilus oryzae (L.). J. Stored Prod. Res. 2003, 39, 375–384. [Google Scholar] [CrossRef]
  55. Lee, S.H.; Do, H.S.; Min, K.J. Effects of essential oil from Hinoki cypress, Chamaecyparis obtusa, on physiology and behavior of flies. PLoS ONE 2015, 10, e0143450. [Google Scholar] [CrossRef] [PubMed]
  56. Lee, G.S.; Hong, E.J.; Gwak, K.S.; Park, M.J.; Choi, K.C.; Choi, I.G.; Jang, J.W.; Jeung, E.B. The essential oils of Chamaecyparis obtusa promote hair growth through the induction of vascular endothelial growth factor gene. Fitoterapia 2010, 81, 17–24. [Google Scholar] [CrossRef] [PubMed]
  57. Kim, E.H.; Kang, S.Y.; Park, B.I.; Kim, Y.H.; Lee, Y.R.; Hoe, J.H.; Choi, N.Y.; Ra, J.Y.; An, S.Y.; You, Y.O. Chamaecyparis obtusa suppresses virulence genes in Streptococcus mutans. Evid.-Based Complement. Altern. Med. 2016, 2016, 2396404. [Google Scholar] [CrossRef]
  58. Takao, Y.; Kuriyama, I.; Yamada, T.; Mizoguchi, H.; Yoshida, H.; Mizushina, Y. Antifungal properties of Japanese cedar essential oil from waste wood chips made from used sake barrels. Mol. Med. Rep. 2012, 5, 1163–1168. [Google Scholar] [CrossRef]
  59. Bajpai, V.K.; Sharma, A.; Kim, S.H.; Baek, K.H. Phenolic content and antioxidant capacity of essential oil obtained from sawdust of Chamaecyparis obtusa by microwave-assisted hydrodistillation. Food Technol. Biotechnol. 2013, 51, 360–369. [Google Scholar]
  60. Hong, C.U.; Kim, C.S.; Kim, N.G.; Kim, Y.H. Composition of essential oils from the leaves and the fruits of Chamaecyparis obtusa and Chamaecyparis pisifera. J. Korean Soc. Biotechnol. 2001, 44, 116–121. [Google Scholar]
  61. Yang, J.K.; Choi, M.S.; Seo, W.T.; Rinker, D.L.; Han, S.W.; Cheong, G.W. Chemical composition and antimicrobial activity of Chamaecyparis obtusa leaf essential oil. Fitoterapia 2007, 78, 149–152. [Google Scholar] [CrossRef]
  62. Bae, M.S.; Park, D.H.; Choi, C.Y.; Kim, G.Y.; Yoo, J.C.; Cho, S.S. Essential oils and non-volatile compounds derived from Chamaecyparis obtusa: Broad spectrum antimicrobial activity against infectious bacteria and MDR (multidrug resistant) strains. Nat. Prod. Commun. 2016, 11, 693–694. [Google Scholar] [CrossRef]
  63. Kim, M.G.; Lee, H.S. Volatile Constituents of Essential Oils Extracted from Two Varieties of Chamaecyparis pisifera in Korea. J. Essent. Oil-Bear. Plants 2012, 15, 364–367. [Google Scholar] [CrossRef]
  64. Song, H.J.; Yong, S.H.; Kim, H.G.; Kim, D.H.; Park, K.B.; Shin, K.C.; Choi, M.S. Insecticidal activity against Myzus persicae of terpinyl acetate and bornyl acetate in Thuja occidentalis essential oil. Horticulturae 2022, 8, 969. [Google Scholar] [CrossRef]
  65. Korea Forest Service. National Forest Inventory Data. Available online: https://kfss.forest.go.kr/stat/ptl/article/articleDtl.do (accessed on 23 May 2023).
  66. Cambero, C.; Sowlati, T. Assessment and optimization of forest biomass supply chains from economic, social and environmental perspectives—A review of literature. Renew. Sustain. Energy Rev. 2014, 36, 62–73. [Google Scholar] [CrossRef]
  67. Wood, S.M.; Layzell, D.B. A Canadian Biomass Inventory: Feedstocks for a Bio-Based Economy-Final Report; BIOCAP CAnada Foundation: Kingston, ON, Canada, 2003. [Google Scholar]
  68. Figueiredo, A.C.; Barroso, J.G.; Pedro, L.G.; Scheffer, J.J. Factors affecting secondary metabolite production in plants: Volatile components and essential oils. Flavour Fragr. J. 2008, 23, 213–226. [Google Scholar] [CrossRef]
  69. Lier, M.; Köhl, M.; Korhonen, K.T.; Linser, S.; Prins, K. Forest relevant targets in EU policy instruments-can progress be measured by the pan-European criteria and indicators for sustainable forest management? For. Policy Econ. 2021, 128, 102481. [Google Scholar] [CrossRef]
  70. Williams, L.R.; Lusunzi, I. Essential oil from Melaleuca dissitiflora: A potential source of high quality tea tree oil. Ind. Crops Prod. 1994, 2, 211–217. [Google Scholar] [CrossRef]
  71. Posadzki, P.; Alotaibi, A.; Ernst, E. Adverse effects of aromatherapy: A systematic review of case reports and case series. Int. J. Risk Saf. Med. 2012, 24, 147–161. [Google Scholar] [CrossRef]
  72. Sarkic, A.; Stappen, I. Essential oils and their single compounds in cosmetics—A critical review. Cosmetics 2018, 5, 11. [Google Scholar] [CrossRef]
  73. The European Communities. Labelling of Ingredients in Cosmetics Directive 76/768/EEC Update February 2008. Available online: https://single-market-economy.ec.europa.eu/sectors/cosmetics_en (accessed on 13 September 2023).
  74. Matura, M.; Sköld, M.; Börje, A.; Andersen, K.E.; Bruze, M.; Frosch, P.; Goossens, A.; Johansen, J.D.; Svedman, C.; White, I.R. Not only oxidized R-(+)-but also S-(−)-limonene is a common cause of contact allergy in dermatitis patients in Europe. Contact Dermat. 2006, 55, 274–279. [Google Scholar] [CrossRef]
  75. Matura, M.; Goossens, A.; Bordalo, O.; Garcia-Bravo, B.; Magnusson, K.; Wrangsjö, K.; Karlberg, A.T. Patch testing with oxidized R-(+)-limonene and its hydroperoxide fraction. Contact Derm. 2003, 49, 15–21. [Google Scholar] [CrossRef]
  76. Topham, E.; Wakelin, S. D-limonene contact dermatitis from hand cleansers. Contact Derm. 2003, 49, 108–109. [Google Scholar] [CrossRef]
  77. Karlberg, A.T.; Magnusson, K.; Nilsson, U. Air oxidation of d-limonene (the citrus solvent) creates potent allergens. Contact Derm. 1992, 26, 332–340. [Google Scholar] [CrossRef] [PubMed]
  78. Audicana, M.; Barnaola, G. Occupational contact dermatitis from citrus fruits: Lemon essential oils. Contact Derm. 1994, 31, 183–185. [Google Scholar] [CrossRef] [PubMed]
  79. Turek, C.; Stintzing, F.C. Stability of essential oils: A review. Compr. Rev. Food Sci. Food Saf. 2013, 12, 40–53. [Google Scholar] [CrossRef]
  80. Rudbäck, J.; Bergström, M.A.; Börje, A.; Nilsson, U.; Karlberg, A.T. α-Terpinene, an antioxidant in tea tree oil, autoxidizes rapidly to skin allergens on air exposure. Chem. Res. Toxicol. 2012, 25, 713–721. [Google Scholar] [CrossRef]
  81. Väisänen, T.; Haapala, A.; Lappalainen, R.; Tomppo, L. Utilization of agricultural and forest industry waste and residues in natural fiber-polymer composites: A review. Waste Manag. 2016, 54, 62–73. [Google Scholar] [CrossRef]
  82. Kelkar, V.M.; Geils, B.W.; Becker, D.R.; Overby, S.T.; Neary, D.G. How to recover more value from small pine trees: Essential oils and resins. Biomass Bioenergy 2006, 30, 316–320. [Google Scholar] [CrossRef]
  83. Johansson, J. Collaborative governance for sustainable forestry in the emerging bio-based economy in Europe. Curr. Opin. Environ. Sustain. 2018, 32, 9–16. [Google Scholar] [CrossRef]
  84. ISO 4730:2004; Oil of Melaleuca, Terpinen-4-ol Type (Tea Tree Oil). International Organisation for Standardisation: Geneva, Switzerland, 2004.
  85. Shojaee-Aliabadi, S.; Hosseini, S.M.; Mirmoghtadaie, L. Antimicrobial Activity of Essential Oil. In Essential Oils in Food Processing: Chemistry, Safety and Applications; John Wiley & Sons, Ltd.: Chichester, UK, 2017; pp. 191–229. [Google Scholar]
  86. Chouhan, S.; Sharma, K.; Guleria, S. Antimicrobial activity of some essential oils—Present status and future perspectives. Medicines 2017, 4, 58. [Google Scholar] [CrossRef]
  87. Sharifi-Rad, J.; Sureda, A.; Tenore, G.C.; Daglia, M.; Sharifi-Rad, M.; Valussi, M.; Tundis, R.; Sharifi-Rad, M.; Loizzo, M.R.; Ademiluyi, A.O. Biological activities of essential oils: From plant chemoecology to traditional healing systems. Molecules 2017, 22, 70. [Google Scholar] [CrossRef]
Table 1. Production figures of major commercial essential oils [7].
Table 1. Production figures of major commercial essential oils [7].
Essential OilsProduction Metric TonsMain Production Countries
Orange oils51,000United States, Brazil, Argentina
Cornmint oil32,000India, China, Argentina
Lemon oils9200Argentina, Italy, Spain
Eucalyptus oils4000China, India, Australia, South Africa
Peppermint oil3300India, United States, China
Clove leaf oil1800Indonesia, Madagascar
Citronella oil1800China, Sri Lanka
Spearmint oils1800United States, China
Cedarwood oils1650United States, China
Litsea cubeba oil1200China
Patchouli oil1200Indonesia, India
Lavandin oil Grosso1100France
Table 2. The latest trade data on essential oils provided by trade statistics provided by the Korea Customs Service [8].
Table 2. The latest trade data on essential oils provided by trade statistics provided by the Korea Customs Service [8].
PeriodExport WeightExport ValueImport WeightImport ValueBalance of Trade
202051.11809.6307557,892−54,817
202161.61831.9214562,710−60,565
202243.61650.0187664,510−62,634
Unit: USD/ton.
Table 3. The major constituents, biological activities, and potential application of essential oils extracted from L. kaempferi.
Table 3. The major constituents, biological activities, and potential application of essential oils extracted from L. kaempferi.
Scientific NamesPlant PartsMajor Chemical ProfileBiological ActivitiesApplicationRef.
L. kaempferileavesα-pinene (19.9%),
β-pinene (17.4%),
L-bornyl acetate (6.1%)
[22]
herbicidal effectagriculture industry[22]
anti-dermatophyte effectpharmaceutical industry[23]
woodα-pinene (18.6%),
α-cadinol (6.2%),
cembrene (6.1%)
anti-inflammatory effect
(relieving the allergy)
pharmaceutical industry [24]
Table 7. The major constituents, biological activities, and potential application of essential oils extracted from C. pisifera.
Table 7. The major constituents, biological activities, and potential application of essential oils extracted from C. pisifera.
Scientific NamesPlant PartsMajor Chemical ProfileBiological ActivitiesApplicationRef.
C. pisiferaleaves3-carene
(35.0%)
(−)-bornyl acetate
(19.8%)
α-pinene
(13.0%)
[63]
insecticidal activityagriculture[64]
fruit(−)3-carene (30.3%)
α-pinene (29.4%)
myrcene (15.1%)
[60]
---
Table 8. The forest area of targeted species in South Korea [65].
Table 8. The forest area of targeted species in South Korea [65].
SpeciesThe Forest Area (ha)
1Larix kaempferi (Lamb.) Carriere259,257
2Pinus densiflora Siebold & Zucc.1,321,878
3Chamaecyparis obtusa (Siebold & Zucc.)69,538
Table 9. The allergenic chemical components in P. densiflora and P. koraiensis essential oils.
Table 9. The allergenic chemical components in P. densiflora and P. koraiensis essential oils.
Scientific NamesPlant PartsMajor Chemical ProfileAllergenic Chemical Components in Accordance with EU Directive
P. densifloraleavesα-pinene (21.6%)
limonene (13.1%)
caryophellene
(11.4%)
[30]
limonene
twigsβ-pinene (22.4%)
α-pinene (17.3%)
limonene (15%)
[30]
limonene
P. koraiensisseedα-pinene (29.9%)
D-limonene (19.3%)
Β-pinene (11.2%)
[14]
D-limonene
conesD-limonene (28.0%),
α-pinene (23.9%),
Β-pinene (12.1%)
[42]
D-limonene
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Park, C.; Woo, H.; Park, M.-J. Development of Pinaceae and Cupressaceae Essential Oils from Forest Waste in South Korea. Plants 2023, 12, 3409. https://doi.org/10.3390/plants12193409

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Park C, Woo H, Park M-J. Development of Pinaceae and Cupressaceae Essential Oils from Forest Waste in South Korea. Plants. 2023; 12(19):3409. https://doi.org/10.3390/plants12193409

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Park, Chanjoo, Heesung Woo, and Mi-Jin Park. 2023. "Development of Pinaceae and Cupressaceae Essential Oils from Forest Waste in South Korea" Plants 12, no. 19: 3409. https://doi.org/10.3390/plants12193409

APA Style

Park, C., Woo, H., & Park, M. -J. (2023). Development of Pinaceae and Cupressaceae Essential Oils from Forest Waste in South Korea. Plants, 12(19), 3409. https://doi.org/10.3390/plants12193409

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