Skip to main content

Official Journal of the Japan Wood Research Society

  • Review article
  • Open access
  • Published:

Physiological effects of wood on humans: a review

Abstract

It is empirically known that wood can cause a comfort enhancement effect in humans. On the other hand, not enough scientific knowledge based on evidence-based research is available on this subject. However, data using physiological indices have increasingly accumulated in recent years. This review provides an overview of the current situation for peer-reviewed reports related to the physiological effects of wood. We reviewed reports that elucidated the effects of wood-derived stimulations on the olfactory, visual, auditory, and tactile sensations using physiological indices such as brain activity (e.g., near-infrared spectroscopy) and autonomic nervous activity (e.g., heart rate variability and blood pressure). It became clear that many studies were limited by (1) a small number of participants, mostly aged in their 20s; (2) use of only a single stimulus (e.g., only olfactory or only visual), or (3) an incomplete experimental design. In addition, this review examined the field of forest therapy, for which there is abundant research. Further study is needed to elucidate the physiological effects of wood on humans.

Introduction

In the 7 million years that human species have existed, over 99.99% of our evolution has taken place in a natural environment. Even since the beginning of urbanization with the industrial revolution, less than 0.01% of our species’ time has been spent in an artificial and urbanized environment. It is considered that the human body is adapted to a natural setting [1, 2]. We proceeded with this research based on the hypothesis that highly urbanized and artificial environments cause a state of physiological stress, which manifests as an increase in sympathetic nervous activity, blood pressure, heart rate, and stress hormone. Indeed, over recent decades, there have been reactions to the urbanized environment, suggesting a possible second phase in how we interact with it. For example, the Japanese term “Shinrin-yoku” [3], which means “taking in the forest atmosphere through all of our senses”, was proposed in 1982 by a Forestry Agency secretary in Japan and in 1984, an American clinical psychologist coined the term “Technostress” [4]. Nature therapy, including relaxation by exposure to natural stimuli from forests, urban parks, flowers, and natural wooden materials, is receiving increasing attention, and scientific data in support of this have begun to accumulate in various research fields [5].

In particular, there have been many reports related to forest therapy experiments, for example, these have investigated reduction of prefrontal cortex activity [6], enhancement of parasympathetic nervous activity [718], inhibition of sympathetic nervous activity [711, 1418], reduction of blood pressure [811, 16, 19], reduction of pulse rate [710, 19], and reduction in the concentrations of stress hormone (e.g., cortisol) [711, 19]. Those results demonstrate the relaxation effects of forest therapy.

With respect to wooden material therapy, the original article about the physiological effects of olfactory stimulation response was published in 1992 [20, 21]. However, since then the amount of data collected according to the principles of evidence-based medicine [22] is extremely limited. Early studies on wooden material therapy investigated the effects of temperature and humidity [2326]. These were followed by studies on the effects of stimuli on the senses using subjective evaluation indexes [2732]. More recently, experiments based on physiological response indexes have been conducted.

In this review, our aim was to summarize the peer-reviewed papers that have accumulated since 1992, the year in which the first article on this research area was published, which describe the physiological effects of wood-derived stimuli on humans via the main senses. We also discuss individual differences research, which has recently become an important subject.

Physiological effects of wood on humans

Early investigations on wooden material therapy tended to use only a single indication, such as blood pressure. Recently, it has become more common to make simultaneous measurements of multiple physiological indicators. An example of the experimental apparatus and setup for an olfactory stimulation experiment is shown in Fig. 1.

Fig. 1
figure 1

An example of olfactory stimulation apparatus and setup

Common physiological evaluations include (1) brain activity, (2) autonomic nervous activity, (3) endocrine activity, and (4) immune system activity [33]. Until recently, the most commonly used indicator of brain activity was electroencephalography (EEG), but the mainstream of recent research has been to measure oxygenated hemoglobin (oxy-Hb) concentration in the prefrontal cortex using near-infrared spectroscopy (NIRS). Initial indicators of autonomic nervous activity included blood pressure, heart rate, pupil diameter, and pupillary light reflex, but it is more common now to measure heart rate variability (HRV), which can be separated into evaluations of sympathetic nervous activity and parasympathetic nervous activity. For an endocrine index, the improvement of analytical techniques has enabled the measurement of stress hormones contained in saliva, such as cortisol concentration. Natural killer cell activity is often used as an indicator of immune activity. The physiological indices used to evaluate the physiological effects of wood are discussed further in reviews by Burnard and Kutnar [34] and Tsunetsugu et al. [35].

The present review summarizes the scientific literature on this subject published over the last 25 years (Table 1). There were three inclusion criteria for the studies: (1) publication in the English or Japanese language; (2) publication between January 1992 and August 2016, and (3) only human studies were included. The search for relevant papers was conducted using the PubMed and CiNii databases. We performed separate searches using keyword combinations of terms related to wood and terms related to physiological effects. The terms related to wood or wood-derived components were as follows: “wood”, “wood material”, “natural wooden material”, “Japanese cypress”, “Japanese cedar”, “hinoki”, “sugi”, “hiba”, “α-pinene”, “limonene”, and “cedrol”. The terms related to physiological effects were the following: “brain activity”, “autonomic nervous activity”, “endocrine activity”, “immune activity”, “physiological effects”, and “physiological relaxation”. This search identified 635 references. Other publications cited in the collected papers were then examined and added to our list if relevant. After applying our three inclusion criteria, we retained 41 articles for our review. Here, we have introduced and summarized this literature according to the sensory mode stimulated: olfactory, visual, auditory, and tactile.

Table 1 Overview of research on wooden material therapy

Olfactory stimulation

Conventionally, experience suggests that the smell of wood has a relaxing effect. However, data on the physiological effects on humans have only recently begun to be collected.

In 1992, Miyazaki et al. [21] examined the effect of olfactory stimulation by Taiwan cypress (Chamaecyparis taiwanensis) wood oil and eugenol on blood pressure, pulse rate, coefficient of variation of R–R intervals in the electrocardiogram (ECG), and performance (letter cancellation test). The participants were six male university students aged between 21 and 22 years, and the experiment was conducted in an artificial climate chamber with the temperature set at 25 °C and humidity at 60%. The strength of perceptibility of the stimulus was adjusted from “easily sensed” to “slightly sensed” on average, and the stimulation was administered for a duration of 30 min. After olfactory stimulation by the Taiwan cypress wood oil, the systolic blood pressure of the participants decreased by 6%, which is considered a meaningful reduction (for comparison, the difference between the high-normal blood pressure of 130 mmHg and normal blood pressure of 120 mmHg is 8.3%). Task performance increased on average by 4%, although this change was not statistically significant. In contrast, in tests using eugenol, a component of the clove oil used in dental disinfectants and rated as “uncomfortable” to smell, olfactory stimulation resulted in an increase in pulse rate of 6%. In 1994, Miyazaki et al. [36] investigated the effects of the different concentration of Taiwan cypress wood oil on blood pressure, pupillary light reflex, and performance. Six female university students aged between 21 and 27 years (mean 22.0 years) participated in this study. To test the perceptibility of the stimulus, three concentrations of Taiwan cypress wood oil were established: “weak”, “easily sensed”, and “strong”. The experiment was conducted in a soundproof artificial climate chamber with the temperature, humidity, and illuminance set at 25 °C, 50%, and 230 lx, respectively. After olfactory stimulation with Taiwan cypress wood oil rated as a “strong” smell, the participants’ diastolic blood pressure decreased by 8% and their maximum constriction acceleration, which reflects autonomic nervous activity, increased by 17%. There was no significant difference; however, the task performance increased by approximately 10% on average.

Li et al. [37] examined the effects of Japanese cypress (Chamaecyparis obtusa) wood oils on endocrine and immune activity. The participants were 12 male instructors aged between 37 and 60 years who worked at a university, who stayed for three nights in a room at an urban hotel where Japanese cypress wood oil was vaporized with a humidifier. After this, the concentrations of adrenaline and noradrenaline in the participants’ urine were reduced and natural killer cell activity was induced. Thus, olfactory stimulation by Japanese cypress wood oil brought about improvements in immune functions.

Several studies have focused on olfactory stimulation with Japanese cedar (Cryptomeria japonica), a common and familiar coniferous tree in Japan. Tsunetsugu et al. [38] revealed the effects of olfactory stimulation by Japanese cedar wood chips on the prefrontal cortex activity and blood pressure of 14 male university students. The participants were seated in an indoor artificial climate chamber with the temperature, humidity, and illuminance set at 25 °C, 60%, and 50 lx, respectively. Olfactory stimuli were presented to the participants as follows: the Japanese cedar chips were placed into a smell bag; this bag was filled with 24 L of indoor air, which became saturated with volatile compounds from the chips; and a smell supply device delivered a flow of 2–3 L/min of this scented air approximately 15 cm under the participant’s nose. The strength of perceptibility of the stimulus was adjusted from “weak” to “slightly sensed” on average, and the duration of the stimulation was approximately 60–90 s. Following this olfactory stimulation with Japanese cedar chips, the participants showed a reduction of total hemoglobin (total Hb) concentration in the left and right prefrontal cortex and decreased systolic blood pressure, indicating that the olfactory stimulation had a physiologically relaxing effect. Matsubara and Kawai [39] investigated the effects of olfactory stimulation with the volatile organic compounds emitted from interior walls made of Japanese cedar on 16 male university students aged between 21 and 28 years (mean 23.5 years), who performed arithmetic tasks (the Uchida–Kraepelin test) for repeated cycles of 15 min of work and 5 min of rest. As a control, the participants undertook similar work in a room without Japanese cedar interior wall panels. Under the control condition, the participants’ salivary chromogranin A concentration, which is known to be a stress marker, was higher after completing the task than before the task. In contrast, the change between pre- and post-work measurements under the Japanese cedar condition was not significant.

There have been several studies using hiba (Thujopsis dolabrata) wood flour and essential oil as olfactory stimulation. Terauchi et al. [40] examined the effects of olfactory stimulation of hiba wood flours on contingent negative variation (CNV) and EEG readings. The participants were ten university and graduate students (five male and five female) aged between 20 and 26 years. The strength of perceptibility of the stimulus was adjusted to “easily sensed” on average. The results of olfactory stimulation with hiba flours showed a decrease in the early CNV amplitudes at the frontal midline (Fz) and an increased EEG alpha/beta wave ratio at the vertex of the head (Cz), indicating that this olfactory stimulation had a calming effect. However, contradictory results have also been reported. Hiruma et al. [41] investigated the influence on CNV of olfactory stimulation by hiba oil. Although the sensory intensity was not indicated in the report, the amplitude of the early and late CNV components were larger, and the reaction time to a click–flash task shorter, under the hiba oil condition than under the control condition with an absence of olfactory stimulation. This indicates that olfactory stimulation with hiba oil had an awakening effect.

Other types of wood have been studied. Tsunetsugu et al. [42] investigated the effects of olfactory stimulation with Japanese mountain cherry (Cerasus jamasakura) wood chips on prefrontal cortex activity and autonomic nervous activity in 20 male university students (mean age 24.2 years). The strength of perceptibility of the stimulus was adjusted to “easily sensed”, and the duration of the stimulation was 2 min. Olfactory stimulation by Japanese mountain cherry wood chips reduced oxy-Hb concentration in prefrontal cortex, pulse rate, and salivary amylase activity. Using EEG, Fukuda and Kaneko [43] examined the effects of olfactory stimulation on brain activity by wood specimens from 15 major species of tree found in Japan. Olfactory stimulation by Japanese umbrella-pine (Sciadopitys verticillata), Japanese white pine (Pinus parviflora var. parviflora), and Japanese zelkova (Zelkova serrata) resulted in an increased incidence of alpha waves at the post-stimulation measurement compared with the pre-stimulation measurement, indicating that these olfactory stimulations had a calming effect.

The different olfactory effects on human physiology that result from different wood-drying methods have also been investigated. Ikei et al. [44] compared the physiological effects of olfactory stimulation by air-dried and high-temperature-dried Japanese cypress chips. The air-dried wood was produced through natural drying processes over 45 months. The high-temperature-dried wood was produced using steam heating drying equipment, which can dry at a high temperature and high speed. The experiment was conducted with 19 female university students (mean age 22.5 years) in a soundproof artificial climatic chamber with the temperature, humidity, and illuminance set at 25 °C, 50%, and 230 lx, respectively. The Japanese cypress chips (80 g) were placed into a smell bag, the smell bag was filled with 24 L of indoor air, and the air saturated with volatile compounds of chips was delivered at a flow of 3 L/min approximately 10 cm under the participant’s nose using a smell supply device. A crossover trial to eliminate any effects due to the order of olfactory stimulation was performed. Ten of the participants were administrated the olfactory stimulation condition first followed by the control condition. The other nine participants received the control first and then the olfactory stimulation. The strength of perceptibility of the stimulus was adjusted from “weak” to “slightly sensed” on average, and the oxy-Hb concentrations in the prefrontal cortex of the participants was measured using near-infrared time-resolved spectroscopy (TRS) throughout the 90-s duration of stimulation. Olfactory stimulation by air-dried wood chips reduced the oxy-Hb concentrations in the right and left prefrontal cortices, whereas these remained unchanged with the high-temperature-dried wood chips; the difference between the two stimulations was statistically significant. This clarified that the prefrontal cortex activity by olfactory stimulation by wood varied according to the wood-drying method.

Single substance inhalation experiments using the main volatile components of wood such as α-pinene and limonene have also been conducted following the same experimental design as in the reports already described [38, 45, 46]. Tsunetsugu et al. [38] investigated the effects of olfactory stimulation by α-pinene and limonene on blood pressure. The strength of perceptibility of the stimulus was adjusted to “slightly sensed” on average, and the blood pressure of the participants was measured every second throughout the 90-s duration of stimulation. Inhalation of α-pinene and limonene reduced systolic blood pressure. Joung et al. [45] also examined olfactory stimulation by d-limonene on autonomic nervous activity by using HRV as an indicator in 13 female university students (mean age 21.5 years). HRV measurements provides two important results: the high-frequency (HF) power, which reflects parasympathetic nervous activity (known to increase during relaxation); and the ratio of low-frequency (LF) to HF, presented as either LF/HF or LF/(LF + HF), which reflects sympathetic nervous activity (known to increase during arousal or stress). In this study, inhalation of d-limonene for 90 s increased HF power by 26.4%. It also reduced the heart rate compared with the control condition (air), suggesting that d-limonene induces physiological relaxation effects. No significant difference was observed in the LF/HF ratio. Ikei et al. [46] investigated the physiological effect of olfactory stimulation on heart rate variability with α-pinene. Inhalation of this for 90 s increased parasympathetic nervous activity by 46.8% and reduced heart rate by 2.8% compared with control (air), indicating physiological relaxation. No significant difference was observed in the LF/(LF + HF) ratio. For comparison, research on forest therapy [10] found an increase in HF power to 102.7% from walking in forests and 55.0% from viewing forest scenery, indicating substantial physiological relaxation effects. In addition, a difference of 21% has been reported when viewing fresh rose flowers [47], and 19.2% when smelling the scent of fresh rose flowers [48] from a sitting position.

Several studies have been conducted in Japan involving inhalation of cedrol, a major component of Japanese cedar tree wood. Dayawansa et al. [49] reported the effects of olfactory stimulation by cedrol on the autonomic nervous activity of 26 Japanese participants (10 male and 16 female, mean age 24 years). The participants were exposed to olfactory stimulation by cedrol for 10 min. This reduced the participants’ heart rate, systolic and diastolic blood pressure, suppressed sympathetic nervous activity, and enhanced parasympathetic nervous system activity compared with the control condition (air). Yada [50] examined effects of olfactory stimulation by cedrol on the autonomic nerve activity of Norwegian, Thai, and Japanese females. The miosis rate (the ratio of the change in pupil diameter after a light stimulus to the initial pupil diameter) in the pupillary light reflex was measured before and after cedrol inhalation. The miosis rate increased after cedrol exposure in the subjects of all three nationalities, suggesting that parasympathetic nervous activity had become dominant. Sadachi et al. [51] investigated the effects of olfactory stimulation by cedrol on the autonomic nerve activity of American female, following the same experimental design. In addition, Umeno et al. [52] investigated the effects on the autonomic nerve activity of direct cedrol inhalation into the lower airway in 11 males who had undergone a total laryngectomy. Compared to the pre-stimulation condition (air), direct inhalation of cedrol for 10 min reduced the participants’ systolic and diastolic blood pressure and sympathetic nervous activity, and increased their parasympathetic nervous activity. Following the same experimental design with the same laryngectomized participants, Hori et al. [53] investigated the effects of direct cedrol inhalation on brain activity, using regional cerebral blood flow (rCBF) measured with single-photon emission tomography as the index of brain activity. The rCBF of the hippocampus, an important area in the regulation of emotion and stress, was increased bilaterally during cedrol inhalation.

There have also been studies about the effects of olfactory stimulation by tree leaves. Ikei et al. [54] investigated the effects of olfactory stimulation by Japanese cypress leaf oil on brain activity and autonomic nervous activity following the same experimental design as in the studies of Ikei et al. and Joung et al. already described [44, 45]. The participants were 13 female university students (mean age 21.5 years). Olfactory stimulation by Japanese cypress leaf oil induced a reduction in oxy-Hb concentration in the right prefrontal cortex and increased parasympathetic nervous activity (the HF power of HRV) by 34.5% compared to the control condition, indicating that olfactory stimulation by Japanese cypress leaf oil can induce physiological relaxation. Matsubara et al. [55] examined the effects on brain and autonomic nervous activity of Siberian fir (Abies sibirica) leaf oil during and after the performance of a sustained task on a visual display terminal (VDT). Nine male university students (mean age 22 years) inhaled air (control condition) or the odorant (Siberian fir leaf oil condition) for a total of 40 min (a 5-min baseline before performing the task, a 30-min VDT task, and a 5-min recovery period after the task). Compared with the control condition, the participants’ heart rate and alpha band power after the task in the presence of Siberian fir leaf oil were decreased and the theta band power was increased. Matsubara et al. [56] also investigated the effects of (−)-bornyl acetate, one of main components contained in the leaves of the Siberian fir, following the same experimental design. After the VDT task in the presence of (−)-bornyl acetate, the sympathetic nervous activity was decreased and the theta band powers increased compared with task performed under the control condition. However, it has been reported that olfactory stimulation by bay tree (Laurus nobilis) leaves increased heart rate compared to the control (air) [57].

There were 20 papers reporting studies about olfactory stimulation. Across all of these papers, the number of participants ranged from 6 to 178; however, the number of participants in 15 of these papers ranged from 6 to 19. The participants were aged from 20 to 60 years, but 15 papers included only participants in their 20s. The exposure times to stimulation ranged from 60 s to 3 days, including 60–120 s in eight papers and 10–45 min in nine papers. Notably, in ten papers there was no statistical comparison between stimulation and a control condition, with comparisons made only between pre- and post-stimulation.

In addition to these individual studies, there have been several reviews of olfactory stimulation by wood-derived substances [5, 35, 5860].

Visual stimulation

Studies investigating the effects of visual stimulation of wood have included experiments with wood panels and wooden rooms.

Sakuragawa et al. [61] examined the effects on systolic and diastolic blood pressure of visual stimulation by full-sized Japanese cypress wall panels. The control was white steel wall panels of a similar size. Fourteen male university students individually viewed each type of wall panel for 90 s while sitting in a chair. The participants were then asked to rate the wall panels according to whether they liked them or not. Over the whole group, there was no significant difference in the results for the two types of panel. However, during the visual stimulation involving the Japanese cypress wall panels, systolic blood pressure decreased among the participants who evaluated the Japanese cypress wall panels as “like”, whereas there was no change among the participants who evaluated them as “dislike”. For the white steel wall panels, systolic blood pressure increased in the participants who evaluated them as “dislike”.

The physiological effects of visual stimulation by wooden room interiors have also been reported. Tsunetsugu et al. [6264] investigated the difference in physiological effects of visual stimulation by rooms with different designs and proportions of wood. Actual rooms (13 m2) were built for the study. Living rooms in Japan typically contain approximately 30% wood in their structure. For this study, four actual rooms (all with area 13 m2) were built: a typical wooden living room (30% wood), a room with extra wood added to the walls (45% wood), and a room where almost all of the wall and the entire floor and ceiling were covered with wood (90% wood). Fifteen male university students aged between 19 and 28 years were exposed to the visual stimulation of each room interior for 90 s. Systolic blood pressure, diastolic blood pressure, and pulse rate were continuously measured as an index of physiological reaction. Visual stimulation by the 30% wood room reduced the participants’ diastolic blood pressure and pulse rate, suggesting that this room induced physiological relaxation effects. In contrast, visual stimulation by the 45% wood room increased pulse rate. In a 30% wood room with added wooden pillars and crossbeams (a designed room taking the total wood content to 40%), the participants’ pulse rates increased in a manner similar to that in the room with 45% wood, indicating a state of physiological wakefulness. In the participants’ subjective evaluations, they rated all the wooden room interiors as “comfortable”. These findings demonstrated that variations in the percentage of wood and the design of a wooden living room induced different physiological changes, and suggested that visual stimulation by a room with 30% wood, which is a standard type of living room commercially available in Japan, induced a physiological relaxation effect.

Kimura et al. [65] examined the different effects of visual and olfactory stimulation by four actual-size model rooms (width 2700, depth 3550, and height 2380 mm) that contained different proportions of hiba wood. Systolic blood pressure, diastolic blood pressure, pulse rate, and salivary alpha-amylase were continuously measured as an index of physiological reaction in seven male and seven female university students (mean age 19.9 years). Systolic and diastolic blood pressure decreased following visual and olfactory stimulation by all four rooms. Furthermore, visual and olfactory stimulation by the room with hiba wood coverage of 20.6% resulted in lower salivary amylase activity compared with stimulation by the room with no hiba wood. These results show that different amounts of hiba wood in interior rooms have different effects on autonomic nervous activity. However, the extent of the separate contributions of the visual and the olfactory stimuli to the physiological response are unknown because the participants received both types of stimulation simultaneously in this experiment.

In total, four papers reported the studies of visual stimulation. These included 10–15 participants aged in their 20s, and the exposure times to stimulation ranged from 90 to 120 s. Three of the four studies did not include a statistical comparison between stimulation and a control condition, but instead conducted statistical comparisons only between pre- and post-stimulation.

In addition to these individual studies, there have been several reviews of wood-derived visual stimulation [5, 34, 35, 38, 60, 6668].

Auditory stimulation

Investigation of the effects of auditory stimulation by wood on physiological response included experiments on floor impact sounds in a wooden house.

Sueyoshi et al. [69, 70] examined effects of light floor impact sounds on the EEG and on the systolic and diastolic blood pressure of 14 males aged between 24 and 29 years. The measurements were conducted in a Japanese style room in an experimental two-storied wooden house. Sitting on a chair at the center of the downstairs room, each participant was exposed to light floor impact sounds that were generated for 5 min on the upstairs floor by a tapping machine. Four light floor impact sounds at 54, 63, 73, and 78 dBA and control (the absence of an impact sound, leaving the average background noise level of 47 dBA) were generated randomly for each participant. This showed that as the light floor impact sound level increased, the incidence of alpha and theta waves on the EEG decreased [69], and that an increase in systolic blood pressure immediately after exposure to the light floor impact sounds depended on the level of the sounds [70].

Sueyoshi et al. [71] also investigated the effects of a single heavy floor impact sound on systolic blood pressure and peripheral blood flow in ten males aged between 24 and 29 years. Each participant sat on a chair at the center of the downstairs room and was exposed to a single heavy floor impact sound generated on the upstairs floor with an automobile tire dropped from heights of 50, 100, and 150 cm. This test has been specified in JIS A 1418-2:2000 [72]. The single heavy floor impact sound generated by the tire increased systolic blood pressure and decreased peripheral blood flow, demonstrating that the human body enters a stress state in response to single heavy floor impact sounds.

In total, therefore, there were three papers about auditory stimulation, which included 9–14 participants aged in their 20s. The exposure times to stimulation ranged from 90 s to 5 min. None of the three papers included a statistical comparison between stimulation and a control condition, but instead conducted statistical comparisons only between pre- and post-stimulation.

In addition to the studies, there have been two reviews of auditory stimulation in a wooden house [67, 73].

Tactile stimulation

There have been very few previous reports about the physiological effects of contact with wood or wooden materials.

Morikawa et al. [74] examined the effects on systolic blood pressure and pulse rate of contact with wood or artificial substances. The participants were 19 female students aged between 20 and 29 years. The study showed that contact with a stainless steel plate or denim material resulted in great fluctuations in the systolic blood pressure and pulse rate, whereas contact with Japanese cypress and Japanese cedar wood caused little fluctuation.

Sakuragawa et al. [75] examined differences in the effects of tactile stimulation on human physiology that resulted from materials at different temperatures (cool, room temperature, and warm). Thirteen male university students each touched the surface of each material for 60 s with their eyes closed. This showed the following results: (1) contact with an aluminum plate increased blood pressure, but the increase was inhibited when the aluminum was warmed; (2) contact with an acrylic plastic plate increased blood pressure, with a greater rate of increase in blood pressure when the acrylic plastic plate was chilled; and (3) blood pressure did not change in response to contact with materials made of Japanese cypress, Japanese cedar, or oak (Quercus crispula), and did not increase even when the oak material was chilled. These results demonstrated that the temperature of the material has a considerable influence on the increase in blood pressure caused by contact with artificial materials such as metals and acrylic. In contrast, contact with wood does not increase blood pressure whether cold or at room temperature, showing its suitability as a material.

Only these two papers described tactile stimulation. They included 13 and 19 participants aged in their 20s. The exposure times to stimulation were 60 s in both cases, and both papers conducted statistical comparisons between pre- and post-stimulation only, with no control condition.

In addition, there have been four reviews of tactile stimulation involving wood-derived material [5, 35, 60, 68].

Summary of the physiological effects of stimulation by wood and wooden materials

This review has described scientific reports that elucidated the physiological effects of wood-derived stimulation. Throughout, these reports showed that olfactory, visual, tactile, and auditory stimulation involving wood-derived materials induced physiological relaxation such as reduction of brain activity, enhancement of parasympathetic nervous activity, and inhibition of sympathetic nervous activity, as well as decreased blood pressure, heart rate, and stress hormone level.

Overall, 41 articles and reviews published in the 25-year period from 1992 to 2016 were included in this review. These were distributed across 5-year periods as follows: 5 (1992–1996), 2 (1997–2001), 9 (2002–2006), 15 (2007–2011), and 10 (2012–August 2016). It can be seen that reports about physiological effects of wood on humans have broadly increased gradually.

However, there are several limitations to these studies. First, the number of participants was generally small and a high proportion of the studies only recruited men and women in their 20s. To generalize the findings would require further studies based on larger samples with a greater range of ages (children to the elderly). Second, many studies used a single stimulus such as only olfactory stimulation or only visual stimulation. No study used complex stimulation. Third, in many studies the experimental design was incomplete, often without a control condition, thus basing results only on a comparison with pre-measurement values. Future studies based on an appropriate experimental design should be performed to accumulate data that can be extrapolated to everyday life.

Prospects for the future

It is known that physiological changes can be brought about by wood-derived stimuli, but the response can vary between individuals. It has been demonstrated that individual differences found in studies are not simply artifact but can have an important meaning in forest therapy research [76, 77]. Indeed, individual difference is an important issue for future studies researching the physiological effects of wood. In this section, we introduce the recent approach to explaining individual differences, which is of major importance in the future of wooden material therapy.

It is recognized that considerable individual differences are observed in physiological data related to nature therapy, including wooden material therapy, but there has not yet been a suitable approach for elucidating this variability. However, in forest therapy studies, attempts have been made to elucidate such individual differences using the “law of initial value” advocated by Wilder [78, 79]. This proposes the principle that the direction of the response to a stimulus depends largely on the initial value. Thus, the higher the initial value, the smaller the response to function-raising stimuli and the larger the response to function-depressing stimuli.

Song et al. [76, 77] investigated the individual differences in physiological relaxation effects related to forest therapy from the perspective of this “law of initial value” and showed that individual differences are not just variations but rather are physiological adjustment effects. The forest therapy experiment involved walking for 15 min in forest and urban areas in eight locations across Japan. The participants in each experiment location included 12 male university students in their 20s, with a total of 92 participants for whom data could be obtained (mean age 21.5 years), and the indicators measured were diastolic blood pressure and pulse rate [76]. For each participant, (value after walking) − (value before walking) was calculated for diastolic blood pressure; this showed that the majority of participants experienced reductions in blood pressure after walking in the forest. However, blood pressure increased in some participants, showing that there is great individual variation. The “law of initial value” was therefore applied and the relationship between the absolute value for the participant’s blood pressure before walking in the forest (the initial value) and the change in blood pressure, i.e., (value after walking) − (value before walking), was investigated. This showed a negative correlation between the initial value and the change in value, indicating that blood pressure decreased after walking in the forest in participants whose initial values were high, and values increased in participants with low initial values. A similar relationship was found between the initial value and the change in pulse rate. In contrast, there was no correlation between the initial value and the change in value when the same participants walked in urban areas. Thus, it was concluded that walking in the forest entailed physiological adjustment effects that brought the diastolic blood pressure and pulse rate closer to their ideal values.

As described, the elucidation of individual differences has shown that the forest environment has a physiological adjustment effect. Individual differences in the physiological response to wood-derived stimulation should not be considered as artifact but should be regarded as substance. Elucidation of individual differences is an important research task in wooden material therapy. Future research on the effects of wood should seek to confirm and further clarify the physiological adjustment effect.

Conclusions

This review presented the recent research about the physiological effects of wood on humans. Data on the physiological effects of wood-derived stimulation are extremely limited, but during the last 15 years, physiological data related to wooden material therapy have rapidly accumulated in the context of advances in physiological measurement systems and measurement equipment. In the future, preventive medical effects by wood-derived stimulation, such as stress reduction and improvement in immune function, may potentially be explained through objective data obtained using a range of physiological indicators, including brain activity, autonomic nervous activity, endocrine activity, and immune activity.

References

  1. O’ Grady MA (2015) Silence: because what’s missing is too absent to ignore. J Soc Cult Res 1:1–25

    Google Scholar 

  2. Miyazaki Y, Park BJ, Lee J (2011) Nature therapy. In: Osaki M, Braimoh A, Nakagami K (eds) Designing our future: perspectives on bioproduction, ecosystems and humanity (Sustainability Science Vol. 4). United Nations University Press, Tokyo, pp 407–412

    Google Scholar 

  3. Selhub EM, Logan AC (2012) Your brain on nature: the science of nature’s influence on your health, happiness and vitality. Wiley, New York

    Google Scholar 

  4. Brod C (1984) Technostress: the human cost of the computer revolution. Addison-Wesley, Boston

    Google Scholar 

  5. Song C, Ikei H, Miyazaki Y (2016) Physiological effects of nature therapy: a review of the research in Japan. Int J Environ Res Public Health 13:781

    Article  PubMed Central  Google Scholar 

  6. Tsunetsugu Y, Miyazaki Y (2005) Measurement of absolute hemoglobin concentrations of prefrontal region by near-infrared time resolved spectroscopy: examples of experiments and prospects. J Physiol Anthropol Appl Human Sci 24:469–472

    Article  PubMed  Google Scholar 

  7. Lee J, Park BJ, Tsunetsugu Y, Ohira T, Kagawa T, Miyazaki Y (2011) Effect of forest bathing on physiological and psychological responses in young Japanese male subjects. Public Health 125(2):93–100

    Article  CAS  PubMed  Google Scholar 

  8. Park BJ, Tsunetsugu Y, Kasetani T, Kagawa T, Miyazaki Y (2010) The physiological effects of Shinrin-yoku (taking in the forest atmosphere or forest bathing): evidence from field experiments in 24 forests across Japan. Environ Health Prev Med 15:18–26

    Article  PubMed  Google Scholar 

  9. Tsunetsugu Y, Park BJ, Ishii H, Hirano H, Kagawa T, Miyazaki Y (2007) Physiological effects of “Shinrin-yoku” (taking in the atmosphere of the forest) in an old-growth broadleaf forest in Yamagata prefecture, Japan. J Physiol Anthropol 26:135–142

    Article  PubMed  Google Scholar 

  10. Park BJ, Tsunetsugu Y, Lee J, Kagawa T, Miyazaki Y (2012) Effect of the forest environment on physiological relaxation-the results of field tests at 35 sites throughout Japan. In: Li Q (ed) Forest medicine. Nova Science Publishers, New York, pp 55–65

    Google Scholar 

  11. Lee J, Park BJ, Tsunetsu Y, Kagawa T, Miyazaki Y (2011) Physiological benefits of forest environment: based on field research at 4 sites (in Japanese). Jpn J Hyg 66:663–669

    Article  Google Scholar 

  12. Park BJ, Tsunetsugu Y, Ishii H, Furuhashi S, Hirano H, Kagawa T, Miyazaki Y (2008) Physiological effects of Shinrin-yoku (taking in the atmosphere of the forest) in a mixed forest in Shinano Town, Japan. Scand J For Res 23:278–283

    Article  Google Scholar 

  13. Lee J, Park BJ, Ohira T, Kagawa T, Miyazaki Y (2015) Acute effects of exposure to traditional rural environment on urban dwellers: a crossover field study in terraced farmland. Int J Environ Res Public Health 12:1874–1893

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Lee J, Tsunetsugu Y, Takayama N, Park BJ, Li Q, Song C, Komatsu M, Ikei H, Tyrväinen L, Kagawa T, Miyazaki Y (2014) Influence of forest therapy on cardiovascular relaxation in young adults. Evid Based Complement Alternat Med:834360

  15. Tsunetsugu Y, Lee J, Park BJ, Tyrväinen L, Kagawa T, Miyazaki Y (2013) Physiological and psychological effects of viewing urban forest landscapes assessed by multiple measurements. Landsc Urban Plan 113:90–93

    Article  Google Scholar 

  16. Park BJ, Kasetani T, Morikawa T, Tsunetsugu Y, Kagawa T, Miyazaki Y (2009) Physiological effects of forest recreation in a young conifer forest in Hinokage Town, Japan. Silva Fennica 43:291–301

    Google Scholar 

  17. Park BJ, Tsunetsugu Y, Morikawa T, Kagawa T, Lee J, Ikei H, Song C, Miyazaki Y (2014) Physiological and psychological effects of walking in stay-in forest therapy (in Japanese). Jpn J Hyg 69:98–103

    Article  Google Scholar 

  18. Ikei H, Song C, Kagawa T, Miyazaki Y (2014) Physiological and psychological effects of viewing forest landscapes in a seated position in one-day forest therapy experimental model (in Japanese). Jpn J Hyg 69:104–110

    Article  Google Scholar 

  19. Lee J, Park BJ, Tsunetsugu Y, Kagawa T, Miyazaki Y (2009) The restorative effects of viewing real forest landscapes: based on a comparison with urban landscapes. Scand J For Res 24:227–234

    Article  Google Scholar 

  20. Miyazaki Y, Motohashi Y, Kobayashi S (1992) Changes in mood by inhalation of essential oils in humans I. Effect of essential oils on pupillary light reflex, performance, sensory evaluation and profile of mood states (in Japanese). Mokuzai Gakkaishi 38:903–908

    CAS  Google Scholar 

  21. Miyazaki Y, Motohashi Y, Kobayashi S (1992) Changes in mood by inhalation of essential oils in humans II. Effect of essential oils on blood pressure, heart rate, R–R intervals, performance, sensory evaluation and POMS (in Japanese). Mokuzai Gakkaishi 38:909–913

    CAS  Google Scholar 

  22. Guyatt G (1992) Evidence-based medicine—a new approach to teaching the practice of medicine. JAMA 268:2420–2425

    Article  Google Scholar 

  23. Harada H (1987) Temperature control function of the wood panel wall housing (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 255–264

    Google Scholar 

  24. Hirai N (1987) Temperature adjustment function of woody housing (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 265–279

    Google Scholar 

  25. Maki F, Aoki T (2006) Change of indoor humidity in various living space (in Japanese). Mokuzai Gakkaishi 52:37–43

    Article  CAS  Google Scholar 

  26. Norimoto K, Yamada T (1974) Humidity control function of the wood-based materials (in Japanese). Wood Industry 29:301–305

    Google Scholar 

  27. Sadoh T (1987) Characteristics of touch feeling of the wood (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 195–206

    Google Scholar 

  28. Ono H (1987) Feel of the floor during walking and exercising (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 207–218

    Google Scholar 

  29. Okajima T (1987) Sensory evaluation (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 233–243

    Google Scholar 

  30. Yoshida M (1987) Multivariate analysis of visual, tactile and auditory stimulation (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 242–250

    Google Scholar 

  31. Ohgama T (1987) Preference survey of smell of the wood (in Japanese). In: Yamada T (ed) The science of woody environment. Kaiseisya Press, Otsu, pp 355–364

    Google Scholar 

  32. Nakamura M (2012) Appearance of wood and wooden interior (in Japanese). Mokuzai Gakkaishi 58:1–10

    Article  Google Scholar 

  33. Measurement Research group of Japan Society of Physiological Anthropology (1996) Handbook for the scientific measurement on human science (in Japanese). Gihodo shuppan Co., Ltd., Tokyo

    Google Scholar 

  34. Burnard MD, Kutnar A (2015) Wood and human stress in the built indoor environment: a review. Wood Sci Technol 49:969–986

    Article  CAS  Google Scholar 

  35. Tsunetsugu Y, Park BJ, Miyazaki Y (2010) Trends in research related to “Shinrin-yoku” (taking in the forest atmosphere or forest bathing) in Japan. Environ Health Prev Med 15:27–37

    Article  PubMed  Google Scholar 

  36. Miyazaki Y, Shimagami K, Kobayashi S (1994) Effect of inhalation of Taiwan Hinoki Wood Oils of different concentrations on autonomic nervous reflex and performance (in Japanese). Jpn J Res Emot 1:75–81

    Article  Google Scholar 

  37. Li Q, Kobayashi M, Wakayama Y, Inagaki H, Katsumata M, Hirata Y, Hirata K, Shimizu T, Kawada T, Ohira T, Park BJ, Kagawa T, Miyazaki Y (2009) Effect of phytoncide from trees on human natural killer cell function. Int J Immunopathol Pharmacol 22:951–959

    Article  CAS  PubMed  Google Scholar 

  38. Tsunetsugu Y, Park BJ, Miyazaki Y (2012) Physiological effects of visual, olfactory, auditory, and tactile factors in the forest environment. In: Li Q (ed) Forest medicine. Nova Science Publishers Inc, New York, pp 169–181

    Google Scholar 

  39. Matsubara E, Kawai S (2014) VOCs emitted from Japanese cedar (Cryptomeria japonica) interior walls induce physiological relaxation. Build Environ 72:125–130

    Article  Google Scholar 

  40. Terauchi F, Kubo M, Ohgama T, Aoki H (1996) Effect of odors from coniferous woods on contingent negative variation(CNV) (in Japanese). J Soc Mater Sci 45:397–402

    Article  Google Scholar 

  41. Hiruma T, Yabe H, Sato Y, Sutoh T, Kaneko S (2002) Differential effects of the Hiba odor on CNV and MMN. Biol Psychol 61:321–331

    Article  PubMed  Google Scholar 

  42. Tsunetsugu Y, Kasetani T, Park BJ, Kagawa T, Miyazaki Y (2010) The effects of plant odors in suburban forests: changes in cerebral activity and autonomic nervous activity induced by odors of Yamazakura and Madake (in Japanese). Jpn J Aromather 10:64–72

    Google Scholar 

  43. Fukuda H, Kaneko T (1995) Evaluation of wood by using smell as a measure: preference of smell and EEG (in Japanese). Wood Ind 50:266–268

    Google Scholar 

  44. Ikei H, Song C, Lee J, Miyazaki Y (2015) Comparison of the effects of olfactory stimulation by air-dried and high-temperature-dried wood chips of hinoki cypress (Chamaecyparis obtusa) on prefrontal cortex activity. J Wood Sci 61:537–540

    Article  Google Scholar 

  45. Joung D, Song C, Ikei H, Okuda T, Igarashi M, Koizumi H, Park BJ, Yamaguchi T, Takagaki M, Miyazaki Y (2014) Physiological and psychological effects of olfactory stimulation with d-limonene. Adv Hortic Sci 28:90–94

    Google Scholar 

  46. Ikei H, Song C, Miyazaki Y (2016) Effects of olfactory stimulation by α-pinene on autonomic nervous activity. J Wood Sci 62:568–572

    Article  Google Scholar 

  47. Ikei H, Komatsu M, Song C, Himoro E, Miyazaki Y (2012) The physiological and psychological relaxing effects of viewing rose flowers in office workers. J Physiol Anthropol 33:6

    Article  Google Scholar 

  48. Igarashi M, Song C, Ikei H, Ohira T, Miyazaki Y (2014) Effect of olfactory stimulation by fresh rose flowers on autonomic nervous activity. J Altern Complement Med 20:727–731

    Article  PubMed  Google Scholar 

  49. Dayawansa S, Umeno K, Takakura H, Hori E, Tabuchi E, Nagashima Y, Oosu H, Yada Y, Suzuki T, Ono T, Nishijo H (2003) Autonomic responses during inhalation of natural fragrance of “Cedrol” in humans. Auton Neurosci 108:79–86

    Article  PubMed  Google Scholar 

  50. Yada Y, Sadachi H, Nagashima Y, Suzuki T (2007) Overseas survey of the effect of cedrol on the autonomic nervous system in three countries. J Physiol Anthropol 26:349–354

    Article  PubMed  Google Scholar 

  51. Sadachi H, Nagashima Y, Tojo S (2007) Effects of cedrol on the autonomic nervous system and survey of sleep and stress in USA. J Jpn Cosmetic Sci Soc 31:148–152

    CAS  Google Scholar 

  52. Umeno K, Hori E, Tsubota M, Shojaku H, Miwa T, Nagashima Y, Yada Y, Suzuki T, Ono T, Nishijo H (2008) Effects of direct cedrol inhalation into the lower airway on autonomic nervous activity in totally laryngectomized subjects. Br J Clin Pharmacol 65:188–196

    Article  CAS  PubMed  Google Scholar 

  53. Hori E, Shojaku H, Watanabe N, Kawasaki Y, Suzuki M, de Araujo MF, Nagashima Y, Yada Y, Ono T, Nishijo H (2012) Effects of direct cedrol inhalation into the lower airway on brain hemodynamics in totally laryngectomized subjects. Auton Neurosci 168:88–92

    Article  CAS  PubMed  Google Scholar 

  54. Ikei H, Song C, Miyazaki Y (2015) Physiological effect of olfactory stimulation by Hinoki cypress (Chamaecyparis obtusa) leaf oil. J Physiol Anthropol 34:44

    Article  PubMed  PubMed Central  Google Scholar 

  55. Matsubara E, Fukagawa M, Okamoto T, Ohnuki K, Shimizu K, Kondo R (2011) The essential oil of Abies sibirica (Pinaceae) reduces arousal levels after visual display terminal work. Flavour Frag J 26:204–210

    Article  CAS  Google Scholar 

  56. Matsubara E, Fukagawa M, Okamoto T, Ohnuki K, Shimizu K, Kondo R (2011) (−)-Bornyl acetate induces autonomic relaxation and reduces arousal level after visual display terminal work without any influences of task performance in low-dose condition. Biomed Res 32:151–157

    Article  CAS  PubMed  Google Scholar 

  57. Matsubara E, Fukagawa M, Okamoto T, Fukuda A, Hayashi C, Ohnuki K, Shimizu K, Kondo R (2011) Volatiles emitted from the leaves of Laurus nobilis L. improve vigilance performance in visual discrimination task. Biomed Res 32:19–28

    Article  CAS  PubMed  Google Scholar 

  58. Miyazaki Y (1993) Comfort of wood: physiologial effect of olfactory stimulation (in Japanese). Wood Ind 48:532–536

    Google Scholar 

  59. Miyazaki Y (1998) Kanse (intuition) and wood: physiological and subjective evaluation II (in Japanese). Wood Ind 53:2–6

    Google Scholar 

  60. Miyazaki Y, Song C, Ikei H (2015) Preventive medical effects of nature therapy and their individual differences (in Japanese). Jpn J Physiol Anthropol 20:19–32

    Google Scholar 

  61. Sakuragawa S, Miyazaki Y, Kaneko T, Makita T (2005) Influence of wood wall panels on physiological and psychological responses. J Wood Sci 51:136–140

    Article  Google Scholar 

  62. Tsunetsugu Y, Miyazaki Y, Sato H (2002) The visual effects of wooden interiors in actual-size living rooms on the autonomic nervous activities. J Physiol Anthropol Appl Hum Sci 21:297–300

    Article  Google Scholar 

  63. Tsunetsugu Y, Miyazaki Y, Sato H (2005) Visual effects of interior design in actual-size living rooms on physiological responses. Build Environ 40:1341–1346

    Article  Google Scholar 

  64. Tsunetsugu Y, Miyazaki Y, Sato H (2007) Physiological effects in humans induced by the visual stimulation of room interiors with different wood quantities. J Wood Sci 53:11–16

    Article  Google Scholar 

  65. Kimura A, Sugiyama H, Sasaki S, Yatagai M (2011) Psychological and physiological effects in humans induced by the visual and olfactory stimulations of an interior environment made of hiba (Thujopsis dolabrata) wood. (in Japanese). Mokuzai Gakkaishi 57:150–159

    Article  Google Scholar 

  66. Miyazaki Y, Lee J, Park BJ, Tsunetsugu Y, Matsunaga K (2011) Preventive medical effects of nature therapy (in Japanese). Jpn J Hyg 66:651–656

    Article  Google Scholar 

  67. Tsunetsugu Y, Miyazaki Y (2007) Comfort evaluation of the forest environment and forest-based environmental factors based on the physiological response (in Japanese). Wood Ind 62:442–447

    Google Scholar 

  68. Nyrud AQ, Bringslimark T (2010) Is interior wood use psychologically beneficial? A review of psychological responses toward wood. Wood Fiber Sci 42:202–218

    CAS  Google Scholar 

  69. Sueyoshi S, Miyazaki Y (1995) Physiological and psychological responses to light floor-impact sounds generated by a tapping machine in a wooden house. Mokuzai Gakkaishi 41:293–300

    Google Scholar 

  70. Sueyoshi S, Miyazaki Y, Morikawa T (2004) Physiological and psychological responses to prolonged light floor-impact sounds generated by a tapping machine in a wooden house. J Wood Sci 50:494–497

    Google Scholar 

  71. Sueyoshi S, Miyazaki Y, Morikawa T (2004) Physiological and psychological responses to a heavy floor-impact sound generated by dropping an automobile tire in a wooden house. J Wood Sci 50:490–493

    Google Scholar 

  72. JIS A1418-2:2000 (2000) Acoustics—measurement of floor impact sound insulation of buildings—part 2: method using standard heavy impact sources (in Japanese). Japanese Standard Association, Tokyo, p 15

    Google Scholar 

  73. Sueyoshi S (2004) Evaluation of floor impact sound insulation performance in wooden buildings (in Japanese). Mokuzai Gakkaishi 50:285–293

    Google Scholar 

  74. Morikawa T, Miyazaki Y, Kobayashi S (1998) Time-series variations of blood pressure due to contact with wood. J Wood Sci 44:495–497

    Article  Google Scholar 

  75. Sakuragawa S, Kaneko T, Miyazaki Y (2008) Effects of contact with wood on blood pressure and subjective evaluation. J Wood Sci 54:107–113

    Article  Google Scholar 

  76. Song C, Ikei H, Miyazaki Y (2015) Elucidation of a physiological adjustment effect in a forest environment: a pilot study. Int J Environ Res Public Health 12:4247–4255

    Article  PubMed  PubMed Central  Google Scholar 

  77. Song C, Ikei H, Miyazaki Y (2014) Elucidation of the physiological adjustment effect of forest therapy (in Japanese). Jpn J Hyg 69:111–116

    Article  Google Scholar 

  78. Wilder J (1931) The “law of initial values”, a neglected biological law and its significance for research and practice. Translated from Zeitschrift fur die gesamte Neurologie und Psychiatric 137, 317–338, Psychophysiology. In: Porges SW, Coles MGH (eds) Hutchinson, & Ross Inc. PA, Stroudsburg, pp 38–46

    Google Scholar 

  79. Wilder J (1967) Stimulus and response: the law of initial value. J Wright Press, Bristol

    Google Scholar 

Download references

Acknowledgements

This work was supported by JSPS KAKENHI Grant Number JP16K18200 from Grant-in-Aid for Young Scientists (B) of the Japan Science and Technology Agency (JST), Japan.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yoshifumi Miyazaki.

Additional information

Publishing and availability of open access articles were supported by JSPS KAKENHI Grant Number JP16HP2001.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ikei, H., Song, C. & Miyazaki, Y. Physiological effects of wood on humans: a review. J Wood Sci 63, 1–23 (2017). https://doi.org/10.1007/s10086-016-1597-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10086-016-1597-9

Keywords