Next Article in Journal
Analysis of Spatiotemporal Variability in Extreme Climate and Potential Driving Factors on the Yunnan Plateau (Southwest China) during 1960–2019
Previous Article in Journal
Combination of Using Pairwise Comparisons and Composite Reference Series: A New Approach in the Homogenization of Climatic Time Series with ACMANT
Previous Article in Special Issue
The Relationship between Tree-Ring Growths of Pinus densiflora and Climate from Three Mountains in Central Region, the Republic of Korea
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Role of Aging and Wind in Inducing Death and/or Growth Reduction in Korean Fir (Abies Koreana Wilson) on Mt. Halla, Korea

1
Department of Wood & Paper Science, Chungbuk National University, Chungbuk 28644, Korea
2
Department of Forest Product, Chungbuk National University, Chungbuk 28644, Korea
3
Forest Bioinformation Division, National Institute of Forest Science, Suwon 16631, Korea
*
Author to whom correspondence should be addressed.
Atmosphere 2021, 12(9), 1135; https://doi.org/10.3390/atmos12091135
Submission received: 29 July 2021 / Revised: 31 August 2021 / Accepted: 31 August 2021 / Published: 3 September 2021
(This article belongs to the Special Issue Climatic Messages from Tree Rings)

Abstract

:
The purpose of this study was to investigate the role of strong winds and aging in the death and/or decline in the growth of Korean fir on Mt. Halla in Korea. Bangeoreum (BA-S), Jindalrebat (JD-E), and Youngsil (YS-W) on the southern, eastern, and western slopes of Mt. Halla (ca. 1600 and 1700 m a.s.l.) were selected for the study. The site chronologies were established using more than 10 living Korean firs at each site. Additionally, to date the years and seasons of death of standing/fallen dead Korean firs, 15/15, 14/15, and 10/10 trees were selected at BA-S, JD-E, and YS-W, respectively. After adjusting the age with the period of growth up to the sampling point, the oldest Korean fir found among the living trees was 114 years old at JD-E and the oldest fir among the dead trees was 131 years old at JD-E. Besides this, most of the trees at BA-S and JD-E were found to have died between 2008 and 2015, and at irregular intervals between 1976 and 2013 at YS-W. Also, the maximum number of trees, that is, 62.7% died between spring and summer, followed by 20.9% between summer and autumn, and 16.4% between autumn of the current year and spring of the following year. Abrupt growth reductions occurred at BA-S and JD-E, and have become more significant in recent years, whereas at YS-W, the abrupt growth reduction and recovery occur in a cyclic order. The intensity and frequency of the typhoons increased from 2012, and this trend was in-line with the increased number of abrupt growth reductions at BA-S and JD-E. Therefore, the typhoons of 2012 are considered as the most likely influencing factor in death and/or growth reduction in Korean firs. In contrast, the decline in the growth of the Korean firs located on the windward slope (YS-W) showed a relationship with winds stronger than 25–33 m/s.

1. Introduction

The excellent adaptability of trees to the ever-changing regional and/or local climate has led to their wide geographical distribution [1,2,3]. Also, tree growth depends upon climate [4]. Various studies have reported that trees at high elevations face mortality and/or reduced growth due to climate changes, such as warming, drought, or unexpected natural events caused by warming [5,6,7,8]. In particular, trees in alpine and subalpine regions are highly sensitive to climatic conditions, and because of this, any shift in their range can be related to climate change [9,10].
Korean fir (Abies koreana Wilson), one of the endemic subalpine tree species in the Republic of Korea, is distributed above 1000 m a.s.l. (ca. 35°40′ and 33°50′ N) on Mt. Halla, Jiri, Deogyu, Gaya, Baegun, Yeongchuk, Geumwon, and Songni [11,12,13]. Due to the moisture stress caused by warming and/or additional stresses caused by strong wind and heavy snow, the number of Korean firs has decreased so markedly [14,15,16,17,18] that the species had been listed as “Endangered” in the RED LIST of the International Union for Conservation of Natural Resources (IUCN) [19].
Mt. Halla, which is located on Jeju Island, is a UNESCO Biosphere Reserve and World Heritage Site and also the highest mountain (1950 m a.s.l.) in the Republic of Korea. The mountain has important ecological value due to its wide biological diversity [20,21]. The mountain range is also home to the largest pure Korean fir forests in the Republic of Korea [22]. However, over the last 10 years, the number of Korean firs on Mt. Halla has severely declined from 738.3 ha in 2006 to 626.0 ha in 2015 (by 15.2% and 112.3 ha) [14,23]. Although spring drought has been declared as the main factor influencing the decline of the Korean fir on Mt. Halla [18,24,25], strong winds and aging have also been considered as potential drivers of the decay.
Jeju Island is a volcanic island and is well known for the strong wind and typhoons that come from the Pacific Ocean, mainly in the summer [26]. During winter, Jeju Island is strongly affected by winter cold-air masses from Siberia, and during summer, it is affected by monsoons and tropical cyclones (typhoons) from the Pacific Ocean that bring heavy rainfall and strong winds predominantly blowing from the southwest [27,28]. Strong wind at high elevations is a stress factor for tree growth because it triggers all sorts of detrimental actions, such as the falling of leaves, breaking of branches, shaking of the root system, or removal of snow, which acts as a water reservoir for the tree growth in spring [29,30,31]. Therefore, a better understanding of the effects of strong winds on tree growth would help to diagnose the reasons for tree death and/or the decline in their growth.
Tree-ring monitoring of Korean fir [24,32,33,34,35,36], even with the oldest looking trees, has revealed that this species does not live for hundreds of years [23]. According to the records published to-date, the oldest Korean fir was 235 years old [17]. In most cases, the ages at breast height were less than 100 years old. Therefore, the Korean fir is considered to live for only a hundred years [27]. Korean firs belong to the Abies species, which have a relatively short life span [37].
The purpose of the current study was to further investigate the role of strong winds and aging, the primary influencers, in the death and/or decline in the growth of Korean fir on Mt. Halla. To this end, the year of death and abrupt growth reduction in the Korean fir on Mt. Halla were analyzed using the tree-ring technique. The results of such an analysis will help to improve our understanding of the various causes of the death and/or decline in growth of the Korean fir on Mt. Halla.

2. Materials and Methods

2.1. Study Sites and Sampling in the Field

Study sites were selected on the southern (Bangaeorum: BA-S), eastern (Jindalrebat: JD-E), and western (Youngsil: YS-W) slopes of Mt. Halla on Jeju Island (Figure 1) at elevations between ca. 1600 and 1700 m a.s.l. (Table 1). Mt. Halla is the tallest national park with a height of 1950 m a.s.l. (Baekrokdam) in the Republic of Korea. Jeju Island has a humid subtropical climate characterized by hot humid summers and cool winters due to the influence of the East Asian monsoon [26]. The annual mean temperature and total precipitation calculated for the last 32 years (1988–2020) from the meteorological stations located at the east, west, south and north of Jeju Island were 16.1 °C (14.4–17.8 °C) and 1657 mm (697–2971 mm), respectively (Figure 2). The warmest and coldest months are August and January with a mean temperature of 26.8 °C (23.7–29.4 °C) and 6.2 °C (2.3–9.4 °C), respectively, and the wettest and driest months are August and December with precipitation of 272 mm (39–927 mm) and 55 mm (2–191 mm), respectively. Approximately 42.7% of the precipitation occurs in the summer (June–August).
The sample trees were selected based on whether they were living, standing dead, or fallen dead (Figure 3). A minimum of 10 Korean firs in each group were studied using tree-ring analysis (Table 1). The size of the firs at BA-S was smaller than those at JD-E and YS-W. Considering the size differences, Korean firs thicker than 10 cm at breast height were selected at BA-S and thicker than 15 cm at JD-E and YS-W for the tree-ring analysis. The first sampling at YS-W was done in 2017, followed by JD-E in 2018 and BA-S in 2019. Two tree-ring core samples were extracted from the sample trees at breast height using an increment borer of diameter 5.12 mm. To avoid compression and reaction in the wood caused by slope [4], the tree-ring cores were collected in a parallel direction to the contour of the slope [25]. For the inclined stems, the increment cores were sampled between the upper and lower sides.

2.2. Tree-Ring Measurement and Cross-Dating

Before measuring the ring width, the increment cores were mounted with their cells vertically aligned and the cross-planes were sanded using a belt sander. The sanding began with #80 sandpaper through #120 and #360 and up to #600 until the ring boundaries were clearly visible [38]. The annual ring widths were measured to the nearest 0.01 mm using the LINTAB (Rinntech, Germany) measurement system.
Cross-dating was applied to establish the site chronologies for BA-S, JD-E, and YS-W using ring-width time series from the living trees. The site chronologies were used to date the year of death of the Korean fir by testing the synchronization between the individual ring-width time series from the dead trees and the corresponding site chronologies. The success of the dating was determined by the statistical t-value (Equation (1)) and G value (Equation (2)) run in the TSAP-Win program (Rinntech, Germany) [39,40] and from their graphical synchronization [41].
t = r × n 2 ( 1 r 2 )
where r is the correlation coefficient between the individual ring-width time series and n   is the number of overlapped years.
G ( x , y ) = 1 n 1 i = 1 n 1 [ G i x + G i y ]
  • If ( x i + 1 x i ) > 0, G i x = +1/2, ( y i + 1 y i ) > 0, G i y = +1/2,
  • ( x i + 1 x i ) = 0, G i x = 0, ( y i + 1 y i ) = 0, G i y = 0,
  • ( x i + 1 x i ) < 0, G i x = –1/2, ( y i + 1 y i ) < 0, G i y = –1/2
where G ( x , y ) is the G-value and x i and y i are the measured ring-width values for the i t h year.

2.3. Death of Trees According to Season

The tree rings of conifers consist of thin-walled large-diameter tracheids (earlywood) and thick-walled small-diameter tracheids (latewood) [42]. The initiation and cessation of tree-ring formation in the Korean fir in the subalpine areas of Mt. Deogyu (35°51′ N, 127°44′, 1585–1594 m a.s.l.) are early May and late September, respectively, whereas the transition from earlywood to latewoods occurs between mid-July and early August [43]. Therefore, the earlywood and latewoods in the youngest dead tree ring can be used as a criterion to determine the season in which tree death occurred. Based on the wood cells’ anatomical characteristics, these seasons were determined by the following criteria: (1) if the youngest tree ring has only earlywood, the death of the tree occurred between spring and summer (image on the left in Figure 4); (2) if its latewood formation is incomplete, the tree died between summer and autumn (middle image in Figure 4); and (3) if the latewood formation is complete, the tree died between the autumn of the current year and spring of the following year (image on the right in Figure 4).

2.4. Age Analysis

The increment cores with and without pith (taken at breast height) and the number of tree rings were used to estimate the age of the tree (Figure 5A). When there was no pith in the increment cores, the pith location was first estimated using circles drawn at 1 cm radius intervals on a transparency film (Figure 5B). Next, the number of tree rings was counted from the innermost tree ring to the bark until the sum of the ring widths reached the estimated distance from the innermost tree ring to the estimated pith location (Figure 5C).

2.5. Monitoring of Abrupt Growth Reduction

In the present study, abrupt growth reduction is signified by a marked decrease in the ring width for three years or more [44]. Such an abrupt reduction in growth observed for three consecutive years is considered to be due to natural destruction, such as mechanical injury, destruction of the foliage, land movement, or thinning [4,44]. To investigate the effect of typhoons and strong winds (a type of natural disaster), the abrupt growth reduction was categorized into three classes: class Ⅰ—here the ring-width growth was reduced by 40–55% for three consecutive years or more (light grey in Figure 6); class Ⅱ—the ring width growth was reduced by 56–70% (dark grey in Figure 6); and class Ⅲ—the ring width growth was reduced by more than 70% (black in Figure 6).

3. Results and Discussion

3.1. Site Chronologies and Their Synchronization

All living trees within the same study sites (BA-S, JD-E, and YS-W) were successfully cross-dated with each other (Figure 7). The mean t-values and G values between the individual ring-width time series and the corresponding site chronologies were higher than 8.2 and 72.3%, respectively. The longest mean chronology of 114 years was established at JD-E, followed by 107 years at YS-W and 73 years at BA-S. The highest mean number of trees rings calculated was 66.7 (44–107) at YS-W, followed by 64.9 (36–114) at JD-E and 52.4 (33–73) at BA-S. The site chronology of BA-S showed higher synchronization with JD-E (t-value: 5.7/G value: 65%) than with YS-W (t-value: 2.1/G value: 60%). The synchronization between JD-E and YS-W was lower than the others (t-value: 0.4/G value: 63%).
The inter-annual growth variation in the trees was determined by the most limiting factor for their growth [45], as well as their sensitivity to the limiting factor [46,47,48]. The synchronization between the site chronologies reflects the similarity of the growth environment. The lapse rate of the annual mean temperature at the northern and southern slopes was −0.61 °C/100 m and −0.68 °C/100 m, respectively, and the annual solar radiation measured on the northern aspect was lower than that on the southern aspect [28]. Besides these, the literature presents several other differences between the northern and southern slopes of Mt. Hall in terms of slope, soil moisture, and annual precipitation. These site conditions at BA-S showed more similarity to those at JD-E than those at YS-W’s. In other words, the site chronology of BA-S showed more synchronization with JD-E than YS-W (Figure 7).

3.2. Tree Ages

The increment cores with abnormally shaped innermost tree rings due to needles or which were decayed, were not considered for the age estimation to avoid over- or underestimation (Table 2). For the estimation, ca. 2–10 tree rings were added to the actual number of tree rings counted in the increment cores. In living trees, the oldest mean age was estimated as 73 years old at YS-W, followed by JD-E (70 years old) and BA-S (58 years old). The oldest Korean fir among the living trees was 114 years old at JD-E. Among the dead trees, the standing dead trees were older than the fallen dead trees at BA-S (58 > 49 years old) and JD-E (80 > 61 years old); however, they were younger at YS-W (54 < 59 years old). The oldest Korean fir among the dead trees was 131 years old and was found at JD-E.
Among the living Korean fir, the trees distributed at the lowest altitude (1610–1613 m a.s.l.) at YS-W were older than the other sites, followed by JD-E where trees were distributed at the second highest altitude (1672–1683 m a.s.l.) and BA-S at the highest altitude (1692–1700 m a.s.l.). The upper limitation of cold climate relict plants like the Korean fir shifts according to temperature, which is the most sensitive factor for tree growth [7,49,50]. It has been proven that the tree-lines at high altitudes of the European Alps, Indian Himalayas, and Altai Mountains shift upward due to climate warming [51,52,53]. The observed age differences among the study sites with different altitudes can also be attributed to the shift due to climate warming.
Abies species at high elevations grow very slowly when juvenile and are not able to live as long as other tree species [27,37]. It has already been proven that the annual mean growth of the Korean fir on Mt. Halla is 1.2 cm for the first 10 years [23] and Farges fir (A. fargesii Franch.) in the Qinling Mountains in China takes ca. 27 years to grow 100 cm [54]. So, the real tree ages of the Korean firs are at least ca. 27 years older than the estimated ages.
Typically, the Korean firs on Mt. Halla grow in shallow soils of volcanic bedrock, so the old trees are more vulnerable to strong winds and/or drought than the younger ones [23]. Until now, none of the past studies on Mt. Halla have found any Korean firs over 120 years old, where the age was determined from the number of tree rings at breast height [24,25]. Although the oldest Korean fir on the mainland, was reported to be 235 years old [17], most Korean firs are less than ca. 150 years old, according to the ages obtained from the increment cores at breast height [24,25,32,33,34,35].

3.3. Year and Season of Death

The distribution of the year of death of the standing dead Korean fir at JD-E and YS-W was wider than the fallen dead Korean firs (Figure 8). On the other hand, at BA-S, the fallen dead Korean fir showed a wider distribution for the year of death than the standing dead Korean fir. Most of the deaths occurred between 2008 and 2015 at BA-S and JD-E. The deaths at YS-W happened in irregular intervals between 1976 and 2013. From the total number of dead trees (ALL-SD and ALL-FD in Figure 8), most of the standing and fallen dead Korean firs died in 2012 (thirteen trees) and 2013 (nine trees), 28.3% died in these 2 years.
The deaths of the Korean fir at YS-W only occurred in the growing season (spring–autumn) but at BA-S and JD-E they occurred in all seasons (Figure 8). The maximum number of Korean fir, 62.7% (42/67 trees), died between the spring and summer (open bar in ALL-SD and -FD in Figure 8), followed by 20.9% (14/67 trees) between summer and autumn (gray bar in ALL-SD and -FD in Figure 8) and 16.4% (11/67 trees) died between autumn of the current year and spring of the following year (black bar in ALL-SD and -FD in Figure 8).
The death of the trees is actually the result of accumulated stress from competition between the trees for nutrients, water and light [55,56], climate change [57,58], and/or natural catastrophe, e.g., typhoon, insects, extreme drought, heavy precipitation or fire [59,60,61,62,63]. The majority of the studies done on other sites as well as on the current sites [17,25,33] reported that the moisture stress related to temperature warming is the principal cause of death of the Korean fir. Considering the rates of increment in the annual mean temperature and total precipitation from 1993 to 2020, viz. 0.025 °C and 8.13 mm, respectively, with a predominate warming trend, (Figure 2), the moisture stress due to warming is the most influential stress factor for the Korean fir.
Most Korean firs on Mt. Halla grow in the shallow soils of the volcanic bedrock [23]. During summer, their growth is highly affected by summer monsoons and typhoons from the Pacific Ocean [64]. Therefore, the strong wind during summer either blows the trees down or disturbs the biological activities by breaking branches, causing the leaves to drop, or separating root systems from the soils [29,30]. A study from 1975 to 2020 revealed that relatively frequent and strong typhoons occurred in 2012 (Figure 8), which might have played a significant role in blowing Korean firs down at BA-S and JD-E. Therefore, 71.4% of the total fallen dead Korean firs at BA-S and JD-E occurred in spring and summer. Moreover, the standing dead Korean firs found in 2013 could be the result of the typhoons in 2012 as well. On the contrary, the death of Korean firs at YS-W did not occur in any single year. The main wind over Mt. Halla blows from west to east [65]; therefore, the Korean firs at YS-W are usually exposed to strong winds. The moisture stress caused by temperature warming and the continuous winds are the main reasons for the death of the Korean firs in different years at YS-W. The above-mentioned two factors are also responsible for the spatial heterogeneity and various shapes and sizes of the Korean firs at YS-W. Furthermore, the deaths at YS-W occurred during the growing season. This implies that the deaths were highly correlated to disturbances in the biological process during the growing season.

3.4. Abrupt Growth Reduction

The growth rates of living Korean firs that exhibited abrupt growth reduction were 46.7% (7/15) at BA-S, 53.8% (7/13) at JD-E, and 70.0% (7/10) at YS-W (Figure 6). For the standing/fallen dead trees, the abrupt growth reduction rates were 76.9% (10/13)/69.2% (9/13) at BA-S, 58.3% (7/12)/81.8% (9/11) at JD-E, and 66.7% (6/9)/77.8% (7/9) at YS-W. Except at YS-W, the growth rates of the dead Korean firs were found to be higher than those of the living ones.
Notably, the intensity of the abrupt growth reduction at BA-S and JD-E was found to be stronger in recent years, whereas the Korean firs at YS-W showed a repeated cycle of abrupt growth reduction and recovery (Figure 6). Considering the year of death of the individual Korean firs, the abrupt growth reduction at every site was found to be the strongest in the 10 years before the trees died.
The intensity and frequency of typhoons also increased from 2012, and these trends were in line with the increase in the intensity of the abrupt growth reduction at BA-S and JD-E (Figure 6). Except for this pattern, no other conspicuous correlations could be observed between the typhoons and the abrupt growth reduction.
The firs on Mt. Halla grow under a lot of stress, such as wet, drought, hot, cold, strong winds, insects, wildfires, and competition with neighboring plants [6,28,66,67,68]. Trees with relatively lower vitality or that grow under harsh microsite conditions usually form narrow annual rings during periods of such stress—the stress is a limiting factor for growth [4,44]. Since the dead trees (SD and FD) exhibit a higher rate of abrupt growth reduction than the living trees (LV), it implies that Korean firs, which have low vitality and/or grow under unfavorable micro conditions, have a higher possibility of death.
On Jeju Island, strong winds blow typically from the west to east [23,65]. Therefore, the Korean fir at YS-W grows under the influence of this wind. The highest intensity of abrupt growth reduction occurred in 1946 and 2002 at YS-W-LV, in 1972 at YS-W-SD and in 1972 and 2002 at YS-W-FD. The above-mentioned years coincide with those in which typhoons stronger than 25–33 m/sec hit the sites. Since the firs were growing in shallow soils of volcanic bedrock, the roots were loosened and lifted from the soil by these strong winds, thereby causing abrupt growth reductions. This is because if the roots are lifted, the trees are not able to get water from the soil easily and adequately, resulting in a decrease in the tree growth [23]. Unlike YS-W, there was no pronounced effect of strong winds on the growth of the firs at BA-S and JD-E. There were some similar patterns in that the intensity of the abrupt growth reduction and the number of typhoons increased in parallel after 2012. Based on the large number of stand and fallen dead Korean firs at BA-S and JD-E that died in 2012 and 2013 when relatively frequent and strong typhoons occurred (Figure 8), it can be inferred that the strong winds in 2012 played a major role in the death and/or reduction in the growth of Korean firs at BA-S and JD-E. However, strong winds may not always have a direct effect on them.

4. Conclusions

The present study attempted to estimate the age of Korean fir trees growing on Mt. Halla and found that the oldest living Korean fir was 114 years old at JD-E and the oldest dead tree was 131 years old at JD-E, based on the 101 sample trees studied. Since no older Korean fir on Mt. Halla has been reported so far, it can be concluded that the Korean fir is not able to live more than ca. 150 years. Typhoons with an intensity of more than 25–33 m/s at the windward slope (YS-W) showed a strong positive relationship with the death and/or abrupt reduction in the growth of the trees. Additionally, Korean firs on the other slopes (BA-S and JD-E) showed a high death rate and abrupt growth reduction starting from 2012. These findings show that the wind has a direct or an indirect effect on the tree growth, depending on its flow direction. There was no significant difference between the standing and fallen dead trees in regard to the patterns of their year of death and the intensity of the abrupt growth reduction rate. Based on these findings, aging and strong winds can be considered in future research as the primary factors causing the decline in growth of the Korean firs on Mt. Halla together with climate change.

Author Contributions

Conceptualization, J.-W.S., E.-B.C., J.-H.P., Y.-J.K. and H.-I.L.; sampling, J.-W.S., E.-B.C., J.-H.P., Y.-J.K. and H.-I.L.; measurement and cross-dating, Y.-J.K., E.-B.C. and J.-H.P.; formal analysis, J.-W.S., E.-B.C. and J.-H.P.; writing—original draft preparation, J.-W.S.; writing—review and editing, J.-W.S. and E.-B.C.; supervision, J.-W.S.; All authors have read and agreed to the published version of the manuscript.

Funding

This study was funded by the National Institute of Forest Science (NiFoS) (FG0802-2018-01) in the Republic of Korea.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data will be made available at the Tree-Ring Research Center (www.dendro.kr/datasets).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Diez, J.M.; Boone, R.; Bohner, T.; Godoy, O. Frequency-dependent tree growth depends on climate. Ecology 2021, 102, e03284. [Google Scholar] [CrossRef] [PubMed]
  2. Kremer, A.; Ronce, O.; Robledo-Arnuncio, J.J.; Guillaume, F.; Bohrer, G.; Nathan, R.; Bridle, J.R.; Gomulkiewicz, R.; Klein, E.K.; Ritland, K.; et al. Long-distance gene flow and adaptation of forest trees to rapid climate change. Ecol. Lett. 2012, 15, 378–392. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Ahrens, C.W.; Andrew, M.E.; Mazanec, R.A.; Ruthrof, K.X.; Challis, A.; Hardy, G.; Byrne, M.; Tissue, D.T.; Rymer, P.D. Plant functional traits differ in adaptability and are predicted to be differentially affected by climate change. Ecol. Evol. 2020, 10, 232–248. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Schweingruber, F.H. Tree Rings and Environment Dendroecology; Paul Haupt: Berne, Switzerland, 1996. [Google Scholar]
  5. Splechtna, B.E.; Dobrys, J.; Klinka, K. Tree-ring characteristics of subalpine fir (Abies lasiocarpa (Hook.) Nutt.) in relation to elevation and climatic fluctuations. Ann. For. Sci. 2000, 57, 89–100. [Google Scholar] [CrossRef] [Green Version]
  6. Eilmann, B.; Zweifel, R.; Buchmann, N. Fonti, P.; Rigling, A.; Drought-induced adaptation of the xylem in Scots pine and pubescent oak. Tree Physiol. 2009, 29, 1011–1020. [Google Scholar] [CrossRef] [Green Version]
  7. Koo, K.A.; Kong, W.-S.; Park, S.U.; Lee, J.H.; Kim, J. Sensitivity of Korean fir (Abies koreana Wils.), a threatened climate relict species, to increasing temperature at an island subalpine area. Ecol. Model. 2017, 353, 5–16. [Google Scholar] [CrossRef]
  8. Fang, O.; Alfaro, R.I.; Zhang, Q.-B. Tree rings reveal a major episode of forest mortality in the late 18th century on the Tibetan Plateau. Glob. Planet. Chang. 2018, 163, 44–50. [Google Scholar] [CrossRef]
  9. Lenoir, J.; Gégout, J.C.; Marquet, P.A.; de Ruffray, P.; Brisse, H. A significant upward shift in plant species optimum elevation during the 20th century. Science 2008, 320, 1768–1771. [Google Scholar] [CrossRef]
  10. Bell, D.M.; Bradford, J.B.; Lauenroth, W.K. Mountain landscapes offer few opportunities for high-elevation tree species migration. Glob. Chang. Biol. 2014, 20, 1441–1451. [Google Scholar] [CrossRef]
  11. Koo, K.A.; Kim, J.; Kong, W.-S.; Jung, H.; Kim, G. Projecting the potential distribution of Abies koreana in Korea under the climate change based on RCP scenarios. J. Korean Environ. Res. Tech. 2016, 19, 19–30. [Google Scholar]
  12. Shin, S.; Kim, J.-H.; Dang, J.-H.; Seo, I.-S.; Lee, B.Y. Elevational distribution ranges of vascular plant species in the Baekdudaegan mountain range, South Korea. J. Ecol. Environ. 2021, 45, 7. [Google Scholar] [CrossRef]
  13. National Institute of Forest Science (NIFS). Status and Conservation Plan of Endangered Coniferous Forest in Republic of Korea; NIFS: Seoul, Korea, 2019. (In Korean) [Google Scholar]
  14. Kim, N.-S.; Lee, H.-C. A study on changes and distributions of Korean fir in sub-alpine zone. J. Korean Environ. Res. Tech. 2013, 16, 49–57, (In Korean with English abstract). [Google Scholar]
  15. Koh, J.G.; Kim, D.S.; Kim, J.G.; Ko, Y.J. Growth dynamics of Korean fir in Mt. Hallasan. Hallasan Res. Rep. 2015, 14, 9–26, (In Korean with English abstract). [Google Scholar]
  16. National Institute of Forest Science (NIFS). Korean Fir in Hallasan Mountain. The Tale of Tee: The Life and Death of Korean Fir; NIFS: Seoul, Korea, 2016. (In Korean) [Google Scholar]
  17. Park, W.-K.; Seo, J.-W. A dendroclimatic analysis on Abies koreana in Cheonwang-bong area of Mt. Chiri, Korea. Korean J. Quarter. Res. 1999, 13, 25–33, (In Korean with English abstract). [Google Scholar]
  18. Kim, J.-K.; Koh, J.-G.; Yim, H.-T.; Kim, D.-S. Changes of spatial distribution of Korean fir forest in Mt. Hallasan. Korean J. Environ. Ecol. 2017, 31, 549–556, (In Korean with English abstract). [Google Scholar] [CrossRef]
  19. Kim, N.-S.; Han, D.U.; Cha, J.-Y.; Park, Y.-S.; Cho, H.-J.; Kwon, H.-J.; Cho, Y.-C.; Oh, S.-H.; Lee, C.-S. A detection of novel habitats of Abies Koreana by using species distribution models(SDMs) and its application for plan conservation. J. Korean Environ. Res. Tech. 2015, 18, 135–149, (In Korean with English abstract). [Google Scholar]
  20. Lee, K.-J.; Ryu, C.-H.; Choi, S.-H. The study of plant community on Orimok, Yongsil and Donnaeko area in Mt. Halla. Ecol. Resil. Infrastruct. 1992, 6, 25–43, (In Korean with English abstract). [Google Scholar]
  21. Kong, W.-S.; Watts, P. The Plant Geography of Korea: With an Emphasis on the Alpine Zones; Springer Science+Science & Business Media: Berlin, Germany, 2012; Volume 19. [Google Scholar]
  22. Kong, W.-S. Biogeography of native Korean Pinaceae. J. Korean Geograph. Soc. 2006, 41, 73–93, (In Korean with English abstract). [Google Scholar]
  23. Kim, E.-S.; Lee, J.-W.; Choi, I.-J.; Lim, W.; Choi, J.; Oh, C.H.; Lee, S.-H.; Kim, Y.-S. Disturbance in seedling development of Korean fir (Abies koreana Wilson) tree species on higher altitude forests of Mt. Hallasan National Park, the central part of Jeju Island, Korea. J. Ecol. Environ. 2017, 41, 22. [Google Scholar] [CrossRef] [Green Version]
  24. Koo, K.-A.; Park, W.-K.; Kong, W.-S. Dendrochronological analysis of Abies koreana W. at Mt. Halla, Korea: Effects of climate change on the growths. J. Ecol. Environ. 2001, 24, 281–288, (In Korean with English abstract). [Google Scholar]
  25. Seo, J.-W.; Kim, Y.-J.; Choi, E.-B.; Park, J.-H.; Kim, J.-H. Investigation of death years and inter-annual growth reduction of Korean firs (Abies koreana) at Yeongsil in Mt. Halla. J. Korean Environ. Res. Tech. 2019, 22, 1–14, (In Korean with English abstract). [Google Scholar]
  26. Chung, C.-H. Vegetation response to climate change on Jeju Island, South Korea, during the last deglaciation based on pollen record. Geosci. J. 2007, 11, 147–155. [Google Scholar] [CrossRef]
  27. Kim, H.-J.; Lee, K.-O.; You, C.-H.; Uyeda, H.; Lee, D.-I. Microphysical characteristics of a convective precipitation system observed on July 04, 2012, over Mt. Halla in South Korea. Atmos. Res. 2019, 222, 74–87. [Google Scholar] [CrossRef]
  28. Ahn, U.S.; Yun, Y.S. Causes of decline in the Korean fir based on spatial distribution in the Mt. Halla region in Korea: A meta-analysis. Forest 2020, 11, 391. [Google Scholar] [CrossRef] [Green Version]
  29. Nishimura, T.B. Tree characteristics related to stem breakage of Picea glehnii and Abies sachalinensis. For. Ecol. Manag. 2005, 215, 295–306. [Google Scholar] [CrossRef]
  30. Kamimura, K.; Shiraishi, N. A review of strategies for wind damage assessment in Japanese forest. J. For. Res. 2007, 12, 162–176. [Google Scholar] [CrossRef]
  31. Han, A.R.; Jung, J.B.; Park, P.S. Effects of micro-topography on the crown growth of Picea jezoensis under different wind conditions on Mt. Deokyu, Korea. Korean J. Agric. For. Meteorol. 2019, 21, 277–285, (In Korean with English abstract). [Google Scholar]
  32. Park, W.-K. Increasing atmospheric carbon dioxide and growth trends of Korean subalpine conifers. J. Korean For. Soc. 1993, 82, 17–25, (In Korean with English abstract). [Google Scholar]
  33. Lim, J.-H.; Woo, S.-Y.; Kwon, M.J.; Chun, J.H.; Shin, J.H. Photosynthetic capacity and water use efficiency under different temperature regimes on healthy and declining Korean fir in Mt. Halla. J. Korean For. Soc. 2006, 95, 705–710, (In Korean with English abstract). [Google Scholar]
  34. Cho, M.-G.; Chung, J.-M.; Kim, T.-W.; Kim, C.-Y.; Noh, I.; Moon, H.-S. Ecological characteristics of Abies koreana forest on Seseok in Mt. Jiri. J. Clim. Chang. Res. 2015, 6, 379–388, (In Korean with English abstract). [Google Scholar] [CrossRef]
  35. Seo, J.-W.; Jeong, H.-M.; Sano, M.; Choi, E.-B.; Park, J.-H.; Lee, K.-H.; Kim, Y.-J.; Park, H.-C. Establishing tree ring δ18O chronologies for principle tree species (T. cuspidata, P. koraiensis, A. koreana, Q. mongolica) at subalpine zone in Jiri National Park and their correlations with the corresponding climate. J. Korean Wood Sci. Technol. 2017, 45, 661–670, (In Korean with English abstract). [Google Scholar]
  36. Seo, J.-W.; Jeong, H.-M.; Lee, K.-H.; Park, H.-C. Dating the dead years of Korean fir (Abies koreana E.H. Wilson) at Imgeollyeong in Jirisan National Park. J. Natl. Park Res. 2019, 10, 219–223, (In Korean with English abstract). [Google Scholar]
  37. Jacobs, B.F.; Werth, C.R.; Guttman, S.I. Genetic relationships in Abies (fir) of eastern United States: An electrophoretic study. Can. J. Bot. 1984, 62, 609–616. [Google Scholar] [CrossRef]
  38. Gärtner, H.; Nievergelt, D. The core-microtome: A new tool for surface preparation on cores and time series analysis of varying cell parameters. Dendrochronologia 2010, 28, 85–92. [Google Scholar] [CrossRef]
  39. Baillie, M.G.L.; Pilcher, J.R. A simple cross-dating program for tree-ring research. Tree Ring Bull. 1973, 33, 7–14. [Google Scholar]
  40. Eckstein, D.; Bauch, J. Beitrag zur Rationalisierung eines dendrochronologischen Verfahrens und zur Analyse seiner Aussagesicherheit. Forstwiss. Cent. 1969, 88, 230–250. [Google Scholar] [CrossRef]
  41. Choi, E.-B.; Kim, Y.-J.; Park, J.-H.; Pakr, C.-R.; Seo, J.-W. Reconstruction of resin collection history of pine forests in Korea from tree-ring dating. Sustainability 2020, 12, 9118. [Google Scholar] [CrossRef]
  42. Larson, P.R. The Vascular Cambium. Development and Structure; Springer: Berlin/Heidelberg, Germany, 1994. [Google Scholar]
  43. Park, J.-H.; Choi, E.-B.; Park, H.-C.; Lee, N.-Y.; Seo, J.-W. Intra-annual dynamics of cambial and xylem phenology in subalpine conifers at Deogyusan National Park in the republic of Korea. J. Wood. Sci. 2021, 67, 22. [Google Scholar] [CrossRef]
  44. Schweingruber, F.H. Tree Rings: Basic and Applications of Dendrochronology; Springer: Dordrecht, The Netherlands, 1988. [Google Scholar]
  45. Fritts, H.C. Tree Rings and Climate; Academic Press: New York, NY, USA, 1971. [Google Scholar]
  46. Eilmann, B.; Zweifel, R.; Buchmann, N.; Pannatier, E.G.; Rigling, A. Drought alters timing, quantity, and quality of wood formation in Scots pine. J. Exp. Bot. 2011, 62, 2763–2771. [Google Scholar] [CrossRef] [Green Version]
  47. Obojes, N.; Meurer, A.; Newesely, C.; Tasser, E.; Oberhuber, W.; Mayr, S.; Tappeiner, U. Water stress limits transpiration and growth of European larch up to the lower subalpine belt in an inner-alpine dry valley. New Phytol. 2018, 220, 460–475. [Google Scholar] [CrossRef] [Green Version]
  48. Lange, J.; Carrer, M.; Pisaric, M.F.J.; Porter, T.J.; Seo, J.-W.; Trouillier, M.; Wilmking, M. Moisture-driven shift in the climate sensitivity of white spruce xylem anatomical traits is coupled to large-scale oscillation patterns across northern treeline in northwest North America. Glob. Chang. Biol. 2020, 26, 1842–1856. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Dolezal, J.; Jandova, V.; Macek, M.; Mudrak, O.; Altman, J.; Schweingruber, F.H.; Liancourt, P. Climate warming drives Himalayan alpine plant growth and recruitment dynamics. J. Ecol. 2021, 109, 179–190. [Google Scholar] [CrossRef]
  50. Wang, L.; Wang, W.J.; Wu, Z.; Du, H.; Zong, S.; Ma, S. Potential distribution shifts of plant species under climate change in Changbai Mountains, China. Forests 2019, 10, 498. [Google Scholar] [CrossRef] [Green Version]
  51. Leonelli, G.; Pelfini, M.; di Cella, U.M.; Garavaglia, V. Climate warming and the recent treeline shift in the European Alps; the role of geomorphological factors in high-altitude sites. Ambio 2011, 40, 264–273. [Google Scholar] [CrossRef] [Green Version]
  52. Singh, C.P.; Panigrahy, S.; Thapliyal, A.; Kimothi, M.M.; Soni, P.; Parihar, J.S. Monitoring the alpine treeline shift in parts of the Indian Himalayas using remote sensing. Curr. Sci. 2012, 102, 559–562. [Google Scholar]
  53. Gatti, R.C.; Callaghan, T.; Velichevskaya, A.; Dudko, A.; Fabbio, L.; Battipaglia, G.; Ligng, J. Accelerating upward treeline shift in the Altai Mountains under last-century climate change. Sci. Rep. 2019, 9, 7678. [Google Scholar] [CrossRef] [PubMed]
  54. Dang, H.; Zhang, Y.; Zhang, K.; Jiang, M.; Zhang, Q. Age structure and regeneration of subalpine fir (Abies fargesii) forests across an altitudinal rage in the Qinling Mountains, China. For. Ecol. Manag. 2010, 259, 547–554. [Google Scholar] [CrossRef]
  55. Adams, T.P.; Purves, D.W.; Pacala, S.W. Understanding height-structured competition in forests: Is there an R* for light? Proc. Biol. Sci. 2007, 274, 3039–3048. [Google Scholar] [CrossRef]
  56. Craine, J.M.; Dybzinski, R. Mechanisms of plant competition for nutrients, water and light. Funct. Ecol. 2013, 27, 833–840. [Google Scholar] [CrossRef]
  57. Allen, C.D.; Macalady, A.K.; Chenchouni, H.; Bachelet, D.; McDowell, N.; Vennetier, M.; Kitzberger, T.; Rigling, A.; Breshears, D.D.; Hogg, E.H.; et al. A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forest. For. Ecol. Manag. 2010, 259, 660–684. [Google Scholar] [CrossRef] [Green Version]
  58. Adams, H.D.; Macalady, A.K.; Breshears, D.D.; Allen, C.D.; Stephenson, N.L.; Saleska, S.R.; Huxman, T.E.; McDowell, N.G. Climate-induced tree mortality: Earth system consequences. Eos Trans. Am. Geophys. Union 2010, 91, 153–154. [Google Scholar] [CrossRef]
  59. Anderegg, W.R.L.; Hicke, J.A.; Fisher, R.A.; Allen, C.D.; Aukema, J.; Bentz, B.; Hood, S.; Lichsein, J.W.; Macalady, A.K.; McDowell, N.; et al. Tree mortality from drought, insects, and their interactions in a changing climate. New Phytol. 2015, 208, 674–683. [Google Scholar] [CrossRef] [PubMed]
  60. Csilléry, K.; Kunstler, G.; Courbaud, B.; Allard, D.; Lassègues, P.; Haslinger, K.; Gardiner, B. Coupled effects of wind-storms and drought on tree mortality across 115 forest stands from the Western Alps and the Jura mountains. Glob. Chang. Biol. 2017, 23, 5092–5107. [Google Scholar] [CrossRef] [PubMed]
  61. Hood, S.M.; Varner, J.M.; van Mantgem, P.; Cansler, C.A. Fire and tree death: Understanding and improving modeling of fire-induced tree mortality. Environ. Res. Lett. 2018, 13, 113004. [Google Scholar] [CrossRef]
  62. Tzeng, H.-Y.; Wang, W.; Tseng, Y.-H.; Chiu, C.-A.; Kuo, C.-C.; Tsai, S.-T. Tree mortality in response to typhoon-induced floods and mudslides is determined by tree species, size, and position in a riparian Formosan gum forest in subtropical Taiwan. PLoS ONE 2018, 13, e0190832. [Google Scholar] [CrossRef] [Green Version]
  63. Tei, S.; Sugimoto, A.; Yonenobu, H.; Kotani, A.; Maximov, T.C. Effects of extreme drought and wet events for tree mortality: Insights from tree-ring width and carbon isotope ratio in a Siberian larch forest. Ecohydrology 2019, 12, e2143. [Google Scholar] [CrossRef]
  64. Altman, J.; Treydte, K.; Pejcha, V.; Cerny, T.; Petrik, P.; Srutek, M.; Song, J.-S.; Trouet, V.; Dolezal, J. Tree growth response to recent warming of two endemic species in Northeast Asia. Clim. Chang. 2020, 162, 1345–1364. [Google Scholar] [CrossRef]
  65. Kim, T.-H. Rates and factors of path widening in Seongpanak hiking trail of Mount Halla, Jeju Island. Korean Geogr. Soc. 2008, 43, 296–311, (In Korean with English abstract). [Google Scholar]
  66. Kueppers, L.M.; Conlisk, E.; Castanha, C.; Moyes, A.B.; Germino, M.J.; de Valpine, P.; Torn, M.S.; Mitton, J.B. Warming and provenance limit tree recruitment across and beyond the elevation range of subalpine forest. Glob. Chang. Biol. 2017, 23, 2383–2395. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Han, A.R.; Lee, S.K.; Suh, G.U.; Park, Y.M.; Park, P.S. Wind and topography influence the crown growth of Picea jezoensis in a subalpine forest on Mt. Deoyu, Korea. Agric. For. Meteorol. 2012, 166–167, 207–214. [Google Scholar] [CrossRef]
  68. Kashian, D.M.; Turner, M.G.; Romme, W.H.; Lorimer, C.G. Variability and convergence in stand structural development on a fire-dominated subalpine landscape. Ecology 2005, 86, 643–654. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Location of the study sites (□) on Mt. Halla and the meteorological stations (). Baeckrokdam () is the peak of Mt. Halla.
Figure 1. Location of the study sites (□) on Mt. Halla and the meteorological stations (). Baeckrokdam () is the peak of Mt. Halla.
Atmosphere 12 01135 g001
Figure 2. Annual mean temperature and precipitation for the last 32 years (1988–2020) recorded in the east (Seongsan), west (Gosan), south (Seogwipo), and north (Jeju) of Jeju Island.
Figure 2. Annual mean temperature and precipitation for the last 32 years (1988–2020) recorded in the east (Seongsan), west (Gosan), south (Seogwipo), and north (Jeju) of Jeju Island.
Atmosphere 12 01135 g002
Figure 3. Living (left), standing dead (middle) and fallen dead (right) Korean fir (Abies koreana) trees at the study sites.
Figure 3. Living (left), standing dead (middle) and fallen dead (right) Korean fir (Abies koreana) trees at the study sites.
Atmosphere 12 01135 g003
Figure 4. The outmost tree rings (OTR) with earlywood (EW), not completely formed latewood (LW), and completely formed latewood (cLW) from dead Korean firs (Abies koreana).
Figure 4. The outmost tree rings (OTR) with earlywood (EW), not completely formed latewood (LW), and completely formed latewood (cLW) from dead Korean firs (Abies koreana).
Atmosphere 12 01135 g004
Figure 5. Illustration of method used to estimate the age of Korean firs (Abies koreana). (A) Cross-section with directions to extract increment cores with pith (ⓐ) and without pith (ⓑ), (B) estimating the location of the pith, when the increment cores have no pith, and (C) estimating the number of tree rings between the innermost tree ring and the estimated location of pith (ⓒ).
Figure 5. Illustration of method used to estimate the age of Korean firs (Abies koreana). (A) Cross-section with directions to extract increment cores with pith (ⓐ) and without pith (ⓑ), (B) estimating the location of the pith, when the increment cores have no pith, and (C) estimating the number of tree rings between the innermost tree ring and the estimated location of pith (ⓒ).
Atmosphere 12 01135 g005
Figure 6. Comparison of the intensity of abrupt growth reduction (AGR) with the frequency of typhoons. BA-S-LV, -SD, and -FD: Bangaeorum-south slope-living tree, -standing dead tree, and -fallen dead tree; JD-E-LV, -SD, and -FD: Jindalraebat-east slope-living tree, -standing dead tree, and -fallen dead tree; YS-W-LV, -SD, and -FD: Youngsil-west slope-living tree, -standing dead tree, and -fallen dead tree; typhoon intensity: 17–25 m/s; 25–33 m/s; 33–44 m/s; 44–54 m/s.
Figure 6. Comparison of the intensity of abrupt growth reduction (AGR) with the frequency of typhoons. BA-S-LV, -SD, and -FD: Bangaeorum-south slope-living tree, -standing dead tree, and -fallen dead tree; JD-E-LV, -SD, and -FD: Jindalraebat-east slope-living tree, -standing dead tree, and -fallen dead tree; YS-W-LV, -SD, and -FD: Youngsil-west slope-living tree, -standing dead tree, and -fallen dead tree; typhoon intensity: 17–25 m/s; 25–33 m/s; 33–44 m/s; 44–54 m/s.
Atmosphere 12 01135 g006
Figure 7. Comparisons of successfully cross-dated individual ring-width time series of living Korean firs (Abies koreana) (grey lines) with their mean time series, i.e., site chronologies (bold black lines). BA-S-LV: Bangaeorum-south slope-living tree; JD-E-LV: Jindalraebat-east slope-living tree; YS-W-LV: Youngsil-west slope-living tree.
Figure 7. Comparisons of successfully cross-dated individual ring-width time series of living Korean firs (Abies koreana) (grey lines) with their mean time series, i.e., site chronologies (bold black lines). BA-S-LV: Bangaeorum-south slope-living tree; JD-E-LV: Jindalraebat-east slope-living tree; YS-W-LV: Youngsil-west slope-living tree.
Atmosphere 12 01135 g007
Figure 8. Comparison of the number of dead Korean fir (Abies koreana) with the frequency of typhoons. BA-S-SD and -FD: Bangaeorum-south slope-standing dead tree and -fallen dead tree; JD-E-SD and FD: Jindalraebat-east slope-standing dead tree and -fallen dead tree; YS-W-SD and -FD: Youngsil-west slope-standing dead tree and -fallen dead tree; Sp: spring; Su: summer; AuC: autumn of the current year; SpN: spring of the following year; typhoon intensity: 17–25 m/s; 25–33 m/s; 33–44 m/s; 44–54 m/s.
Figure 8. Comparison of the number of dead Korean fir (Abies koreana) with the frequency of typhoons. BA-S-SD and -FD: Bangaeorum-south slope-standing dead tree and -fallen dead tree; JD-E-SD and FD: Jindalraebat-east slope-standing dead tree and -fallen dead tree; YS-W-SD and -FD: Youngsil-west slope-standing dead tree and -fallen dead tree; Sp: spring; Su: summer; AuC: autumn of the current year; SpN: spring of the following year; typhoon intensity: 17–25 m/s; 25–33 m/s; 33–44 m/s; 44–54 m/s.
Atmosphere 12 01135 g008
Table 1. Description of sample trees (Abies koreana) at the study sites, viz. Bangaeorum (BA-S), Jindalrae (JD-E), and Youngsil (YS-W).
Table 1. Description of sample trees (Abies koreana) at the study sites, viz. Bangaeorum (BA-S), Jindalrae (JD-E), and Youngsil (YS-W).
SiteYTree ConditionIDNDBH cm
(Min.–Max.)
Long. (N)/Lat. €/m a.s.l.
Bangae
-orum
2019LivingBA-S-LV1823.1
(12.0–35.0)
126°31′/33°21′/1700
(BA-S) Standing deadBA-S-SD1521.9
(11.0–27.5)
126°31′/33°21′/1694
Fallen deadBA-S-FD1519.3
(13.0–29.0)
126°31′/33°21′/1692
Jindalrae
(JD-E)
2018LivingJD-E-LV1328.2
(21.0–33.0)
126°32′/33°21′/1672
Standing deadJD-E-SD1422.4
(16.0–31.0)
126°32′/33°21′/1674
Fallen deadJD-E-FD1521.1
(16.0–34.0)
126°32′/33°21′/1683
Youngsil
(YS-W)
2017LivingYS-W-LV1022.7
(18.0–26.0)
126°30′/33°21′/1610
Standing deadYS-W-SD1021.2
(16.0–24.5)
126°30′/33°21′/1611
Fallen deadYS-W-FD1021.9
(19.0–25.5)
126°30′/33°21′/1613
Y: sampling year, N: the number of sample trees, DBH: diameter at breast height.
Table 2. Estimated tree ages at breast height of the sample trees (Abies koreana) at the study sites, viz. Bangaeorum (BA-S), Jindalrae (JD-E), Youngsil (YS-W).
Table 2. Estimated tree ages at breast height of the sample trees (Abies koreana) at the study sites, viz. Bangaeorum (BA-S), Jindalrae (JD-E), Youngsil (YS-W).
SiteIDNMean No. of Tree Rings
(Min.–Max.)
Mean Estimated Age
(Min.–Max.)
BangaeorumBA-S-LV16/1855 (37–9)58 (37–85)
(BA-S)BA-S-SD14/1555 (25–89)58 (25–100)
BA-S-FD15/1545 (33–68)49 (33–70)
JindalraeJD-E-LV12/1366 (40–114)70 (40–114)
(JD-E)JD-E-SD10/1474 (59–111)80 (59–131)
JD-E-FD8/1554 (30–69)61 (30–83)
YoungsilYS-W-LV9/1069 (51–106)73 (51–109)
(YS-W)YS-W-SD8/1053 (38–73)54 (38–73)
YS-W-FD9/1056 (46–93)59 (46–96)
N: the number of sample trees used to estimate the ages.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Seo, J.-W.; Choi, E.-B.; Park, J.-H.; Kim, Y.-J.; Lim, H.-I. The Role of Aging and Wind in Inducing Death and/or Growth Reduction in Korean Fir (Abies Koreana Wilson) on Mt. Halla, Korea. Atmosphere 2021, 12, 1135. https://doi.org/10.3390/atmos12091135

AMA Style

Seo J-W, Choi E-B, Park J-H, Kim Y-J, Lim H-I. The Role of Aging and Wind in Inducing Death and/or Growth Reduction in Korean Fir (Abies Koreana Wilson) on Mt. Halla, Korea. Atmosphere. 2021; 12(9):1135. https://doi.org/10.3390/atmos12091135

Chicago/Turabian Style

Seo, Jeong-Wook, En-Bi Choi, Jun-Hui Park, Yo-Jung Kim, and Hyo-In Lim. 2021. "The Role of Aging and Wind in Inducing Death and/or Growth Reduction in Korean Fir (Abies Koreana Wilson) on Mt. Halla, Korea" Atmosphere 12, no. 9: 1135. https://doi.org/10.3390/atmos12091135

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop