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Article

Effects of Soil Amelioration and Vegetation Introduction on the Restoration of Abandoned Coal Mine Spoils in South Korea

1
Department of Bio and Environmental Technology, Seoul Women’s University, Seoul 01797, Korea
2
Division of Ecological Survey, National Institute of Ecology, Seocheon 33657, Korea
3
Division of Forest Restoration Support, Baekdudaegan National Arboretum, Bonghwa 36209, Korea
*
Author to whom correspondence should be addressed.
Forests 2022, 13(3), 483; https://doi.org/10.3390/f13030483
Submission received: 2 December 2021 / Revised: 13 March 2022 / Accepted: 16 March 2022 / Published: 20 March 2022
(This article belongs to the Special Issue Forest Restoration and Secondary Succession)

Abstract

:
In order to ecologically restore coal mine spoils, tolerant species were selected through vegetation surveys on the abandoned coal mine spoils and natural forests established on the poor environment similarly to there. In addition, tolerant species were selected through cultivation experiments in the laboratory. Many C4 plants were included among the tolerant species selected through cultivation experiments. Soil was ameliorated by applying commercial organic fertilizer that can improve both physical and chemical properties of soil at the same time. Vegetation introduced for restoration was prepared by combining plant species tolerant to the degraded environment of coal mine spoils and the reference information. The treatment with a soil ameliorator improved the chemical properties of soil, such as the pH and nutrient contents, and promoted the growth of sample plants significantly. However, additional improvements were required compared with the chemical properties of healthy forest soil. The sites restored by ameliorating soil and introducing tolerant species showed a more similar species composition to the reference sites compared with the afforested and non-restored sites in both lowland and upland areas. However, such restoration did not play a significant role in increasing species diversity or excluding exotic plants. In this respect, more active restoration is recommended.

1. Introduction

Coal mining activities in Korea have been conducted through deep mining processes, because coal deposits are deep underground. Therefore, coal mining activities usually lead to the production of large quantities of waste material, or spoils. Such coal mining debris has been piled up on mountains or discarded in mountain valleys. Therefore, acid mine drainage, barren unvegetated areas, and steep unstable piles of mining waste are frequently left behind after mining. Even when the damaged areas are re-vegetated, exotic or non-local species are usually employed for the rehabilitation of those areas. Consequently, most rehabilitated mine areas form an ecological space dissimilar to the surrounding habitat [1].
This problem has occurred because the ecology of the mined area is not well-understood by rehabilitation practitioners. In reality, untreated deep mining debris does not function as soil by itself because it does not include sufficient organic matter and nutrients. Therefore, ecosystem development in these areas must progress in the same manner as primary succession: the process of ecosystem development on barren surfaces where severe disturbances have removed most vestiges of biological activity. Succession progresses as a result of interactions among plants growing in a given area. The facilitation of growth of new plant species by early colonizers promotes species compositional change to the next successional stage [2,3,4].
A properly planned restoration project attempts to fulfill clearly stated goals that reflect important attributes of the reference ecosystem. Goals are attained by pursuing specific objectives, which are evaluated on the basis of performance standards, also known as design criteria or success criteria. These standards or criteria are largely conceived from an understanding of the reference ecosystem [5,6,7].
Three strategies exist for conducting an evaluation: direct comparison, attribute analysis, and trajectory analysis. In direct comparison, selected parameters are determined or measured in the reference and restoration sites. The parameters considered include aspects of both the abiotic environment and the biota. In attribute analysis, attributes such as species composition, percentage of indigenous species, stability of the system, the physical environment, the presence of normal developmental processes, harmony with the larger ecological matrix, potential threats to the habitat, resilience, and capacity for self-sustenance are used to judge the degree to which each goal has been achieved. Trajectory analysis is an evaluation of trends in restoration area to determine whether the restoration is following its intended trajectory towards the reference condition [5,6,7].
The trajectory of a restoration project may be viewed in terms of ecosystem structure and functioning. A change in both dimensions occurs when habitat is degraded. The fundamental goal of restoration is to return a habitat or ecosystem to a condition as close as possible to its pre-degraded state. Complete restoration would involve a return or a partial return to the original state, whereas other trajectories would result in rehabilitation of the system, or replacement with a different system [8].
To effectively restore degraded areas or to protect existing high-quality areas, we must be able to define the attributes of “normal” and undegraded or “healthy,” habitats as a model. One way of setting a baseline and measuring restoration success is to define the normal “biological integrity” of a system and then measure deviations from this norm. Biological integrity is defined as “the ability to support and maintain a balanced, integrated, adaptive biological system having the full range of elements and processes expected in the natural habitat of a region” [9]. To evaluate the integrity of a site, ecological attributes of the site are compared with those of an “undisturbed” reference.
Many species have been introduced, deliberately and accidentally, into areas where they are not native [10,11]. Often, these exotic species subsequently expand their ranges beyond the place of initial establishment because of advantageous life history strategies [12]. Disturbed lands often provide favorable microhabitats for exotic species equipped with opportunistic or ruderal life history strategies [12,13,14,15]. Unlike in their original habitat, these exotic species can become very aggressive in their newly settled habitat. Therefore, experts in this field view the spread of exotic species as one of the most serious environmental problems, and also consider it a major contributor to biodiversity loss [16]. Restoration practices are recommended as a measure to inhibit the invasion of exotic species [15,17,18]. Restorative treatment reduces the relative coverage of exotic plants, which implies that restoration practices can contribute to conserving and restoring the biological integrity of damaged riverine ecosystems [9,19,20].
Although the restoration projects should be scientifically assessed, most projects are still unevaluated, and conducted evaluations lead to ambiguous results [21,22,23,24,25,26,27]. Furthermore, a consensus on what constitutes a successful restoration project is still lacking. In addition, although restoration programs are being incorporated widely into natural resource strategies from the local to the global level, uncertainty remains as to how to effectively and efficiently execute these efforts [6,28]. However, without an adequate evaluation of restorations, lessons cannot be learned from successes and failures, and the restoration field will not advance [6,22,26,27,29]. Moreover, evaluating the success of restoration projects is crucial to adaptive management, improving the effectiveness of future projects and collaborative learning [30,31].
Evaluating restoration is not straightforward, and what characterizes successful restoration and how best to measure it are highly debated [27,32]. Hobbs and Norton [33] provided a framework to delineate the practice of ecological restoration, including the aims and methodologies that can be used, the expansion of targets for restoration beyond ecology, and the inclusion of historical, social, cultural, political, aesthetic, and moral aspects [34]. However, since then, debates over the goals of restoration [35,36], the influence of climate change [37,38,39], and socioeconomic circumstances [40,41,42,43] have continued. All of these issues affect the definition and evaluation of restoration success, and synthesizing these debates has led to the development of useful indicators [32].
This study was carried out to restore coal mine spoils ecologically and evaluate the effects after restoration. The aim of this study was to restore the coal mine spoils to a level similar to the natural forest by introducing plants. To realize this goal, we applied a soil ameliorator and introduced a selection of tolerant plants that can withstand the degraded environment of coal mine spoils. The restoration effects, first of all, were evaluated based on the effect of the soil ameliorator in terms of improving the chemical properties of soil and promoting the growth of specimen plants. Furthermore, the effects were also evaluated based on vegetation quality. Vegetation quality was evaluated based on species composition, biodiversity, and exotic species rate.

2. Materials and Methods

2.1. Site Description

Sites for carrying out this study were selected in two areas of Dogye-eup (the first area) and Taebaek-si (the second area) in Gangwon province (Figure 1). The first area, ranging vertically from 200 m to 400 m above sea level, was chosen to obtain information for the restoration of coal mining spoils in lowland areas. Exposed outcrops appeared frequently, and soil development was usually poor in forests around the first area. The environmental conditions led to the establishment of a Korean red pine (Pinus densiflora Siebold & Zucc.) forest. Ecological restoration of the coal mine spoils located in this area was practiced by imitating this Korean red pine forest as a reference site. There were two sorts of reclaimed sites in the first area. One site was reclaimed by introducing black locust (Robinia pseudoacacia L.) about 30 years ago, and the other one was afforested by introducing birch (Betula schmidtii Regel.) 10 years ago.
The second area, ranging vertically from 800 to 1000 m above sea level, was chosen to obtain information for the restoration of coal mining spoils in upland areas. Four kinds of reclaimed sites were found in the second area. Alnus incana subsp. Hirsute Turcz. ex Spach., Betula platyphylla var. japonica H. Hara., Lespedeza cyrtobotrya Miq., and Robinia pseudoacacia were introduced to rehabilitate the coal mine spoils of this area 30 years ago. The other site was reclaimed by introducing Lespedeza cyrtobotrya 10 years ago. Surrounding forests chosen as reference site were usually covered with Mongolian oak (Quercus mongolica Fisch. ex Ledeb.) forest.

2.2. Soil Amelioration

Coal waste is severely deficient in nutrients due to its low organic matter content and low pH, and it is not hospitable for plants to establish due to physical defects of the substrate as a planting bed. Organic fertilizer replenishes nutrients in natural organic materials and is considered to be a soil ameliorator that can improve the physical and chemical properties of such coal waste at the same time [1,44]. Therefore, commercial organic fertilizers were adopted and applied as soil ameliorators in this study.

2.3. Selection of Tolerant Species

The tolerant species to realize ecological restoration of coal mine spoils were selected through field surveys on vegetation established on the mountainous land with exposed outcrops and talus with similar environments to coal spoils (the first criterion). In addition, the species that were naturally established flourished in the coal mine spoils as species that does not exist or rarely appear, and especially flourished in the coal mine spoils in comparison with the species composition of reference sites and coal mine spoils (the second criterion).
The tolerant species from laboratory experiments were selected by comparing the growth of sample plants cultivated in the ameliorated pots by adding organic fertilizer and forest soil to pots containing raw coal mine debris (Table 1).

2.4. Restorative Treatment

Our restoration goal was to cover these damaged mountains with vegetation and restore them similarly to existing forests. Barren coal mine debris needs to be ameliorated by introducing a proper soil ameliorator to the level that the introduced plants can survive to realize ecological restoration through the successful settlement of plants. Ecological restoration was carried out by applying a soil ameliorator and introducing tolerant plants to the coal mine spoil dump. The coal mine spoil dump was reshaped to maintain a slope similar to that of the surrounding mountain to ensure stability. Then, coal mine debris was ameliorated by applying an organic fertilizer, which was selected as a suitable ameliorator through the preliminary study. Organic fertilizer was supplied as 6.4 ton/ha and 12.8 ton/ha. Chemical properties of the organic fertilizer are given in Appendix A.
The planting bed was prepared in a size of 5 m × 5 m. Each treatment plot of soil had five replicates for the lowland site and three for the upland site. Sample plants were introduced at 1 m intervals for trees and 50 cm intervals for shrubs and herbaceous plants. The control plot of the soil involved a fresh coal mine debris plot that was not treated with any soil ameliorator. No plants were introduced for restoration to the non-restored plot of vegetation (Figure 2).
The arrangement of tolerant plants to realize ecological restoration was harmoniously planned considering the distribution range of plants in the natural environment, based on the topography and the tolerance ranking for the polluted soil obtained from experimental study. Our restoration plan placed plants for restoration by considering both natural and artificial elements [45,46,47,48]. Upland and lowland restoration models were prepared assuming a Mongolian oak forest and a Korean red pine forest, respectively, by reflecting the spatial distribution patterns of natural vegetation of the corresponding region. In order to create a Mongolian oak forest, Q. mongolica, Betula platyphylla var. japonica, B. schmidtii, Albizia julibrissin Durazz., Styrax japonicas Siebold & Zucc., Acer pseudosieboldianum (Pax) Kom., Rhododendron schlippenbachii Maxim., and Spodiopogon sibiricus Trin. were introduced. P. densiflora, R. mucronulatum, Lespedeza cyrtobotrya, Miscanthus sinensis Andersson., and Arundinella hirta (Thunb.) Tanaka. were introduced to create a Korean red pine forest. Both plots were prepared by hypothesizing a forest with canopy tree, shrub, and herb layers in the future (Figure 3). Each restoration model should avoid heterogeneous choices that do not match the surroundings, considering natural vegetation around the coal mine spoils and exotic plant species which should be thoroughly excluded when tolerant plants are introduced. Among the plants introduced for restoration, three-year-old seedlings were used in the case of woody plants, whereas one-year-old seedlings were used in the case of herbaceous plants.

2.5. Evaluation on Restoration Effects

The restoration effect in soil was evaluated for pH, organic matter, N, P, K, Ca, and Mg contents, and cation exchange capacity (CEC). Soil characteristics (pH, organic matter, Total-N, P, K+, Ca2+, and Mg2+ content and CEC) in the three treatment plots (control, OF 6.4 and OF 12.8) were compared with one-way analysis of variance (ANOVA) and Tukey’s honestly significant difference (HSD) test at α = 0.05 (SAS 2001).
The restoration effect of vegetation was evaluated by comparing species composition, species diversity, and exotic plant ratio with natural reference forests and artificial plantation.

2.6. Soil Analysis

Soil samples were collected in September 2017 from the top 10 cm after removing the litter at five random points in each plot; after which, they were pooled, air-dried at room temperature, and sieved through 2 mm mesh.
Soil properties were diagnosed for pH, and organic matter, Total-N, P, K+, Ca2+, and Mg2+ contents. Soil pH was measured with a bench top probe after mixing the soil with distilled water (1:5 ratio, w/v) and filtering the extract (Whatman No. 44 paper). Organic matter content was obtained by measuring the loss after ignition for four hours in a muffle furnace of 400 °C. Total nitrogen was measured with the micro-Kjeldahl method [49]. Available P was extracted in 1 N ammonium fluoride (pH = 7.0) and exchangeable K+, Ca2+, and Mg2+ contents were measured from the extract by 1 N ammonium acetate (pH = 7.0 for K, Ca and Mg and pH = 4.0 for Al) by ICP (inductively coupled plasma atomic emission spectrometry; Shimadzu ICPQ-1000, Shimadzu Cor., Kyoto, Japan) [50].

2.7. Vegetation Analysis

In the restoration site located in the lowland area, a vegetation survey was carried out for 72 plots. A total of 16 ecologically restored plots were chosen for vegetation survey and 18 reference stands, 5 non-restored plots, and 33 afforested plots by introducing Betula schmidtii (15 plots) and Robinia pseudoacacia (18 plots) were investigated for comparison with the restored plots.
In the other restoration site located in upland, 49 plots were chosen for the vegetation survey. A total of 5 ecologically restored plots were chosen for vegetation survey and 10 reference stands, 3 non-restored plots, and 31 afforested plots by introducing Alnus incana subsp. hirsuta (12 plots), Betula platyphylla var. japonica (9 plots), Lespedeza cyrtobotrya (5 plots), and Robinia pseudoacacia (5 plots) were investigated for comparison with the restored plots.
Plots 10 m × 10 m in size were used for the reference stands and the afforested plots, which are reached mature forest and 5 m × 5 m plots were used for the restored plots and the young, afforested plots (Betula schmidtii plots and Lespedeza cyrtobotrya plots).
The purpose of designation of reference plots was to compare them, as a target community, with the restored plots. Neither soil amelioration nor planting was conducted in the reference plots.
Vegetation data were collected in the restored stands and the reference plots in 2017. All the plant species which occurred in each plot were identified following KPNI [51]. The dominance of each species in each plot was estimated with an ordinal scale (1 for <5% to 5 for >75%), and each ordinal scale was converted to the median value of percentage cover range in each cover class [52]. Importance value of each species was then determined by multiplying the fraction of each species cover to the summed cover of all species in each plot by 100. A matrix of importance values for all species in all plots was constructed and imputed to detrended correspondence analysis (DCA) for ordination [53].
As a measure of species diversity and dominance, a rank abundance curve [54,55,56] was constructed. Percentages of native and alien species to endemic species were also determined for each stand type.
We measured the height and diameter growths of sample plants and compared between the ameliorated and the untreated plot. Plant height and diameter were measured with a measuring tape with 0.5 mm precision and Vernier calipers (NTD12, Mitutoyo Cor., Kanagawa, Japan) with 0.05 mm precision and averaging five randomly chosen stems in each subplot. The height and diameter of sample plants among plots were compared with ANOVA and HSD at α = 0.05 [57].

2.8. Statistical Analysis

All statistical analyses were carried out using Statistical Analysis System (SAS) version 9.1 [57]. For all analyses, we assessed differences using a significance level of at least p = 0.05. Analysis of variance (ANOVA) was performed to compare any differences in the soil environmental factors among pitch pine stands with different stand ages and with the reference oak stand. Tukey’s honestly significant difference method was employed when making multiple comparisons among means.
Detrended correspondence analysis (DCA) is an eigenvector ordination technique based on correspondence analysis (CA or RA). It is especially suited to the analysis of ecological datasets based on sample units and species [53,58]. The differences in species composition among stands restored ecologically (restoration), rehabilitated by applying the silvicultural method, and reference stands were analyzed using DCA.

3. Results

3.1. Selection of Tolerant Species by Field Survey

Tolerant plant species to be introduced for restoration were selected as species which appeared as more than Ⅲ in constancy (frequency 40–60%) in the reference site to ensure a similar species composition to the reference site (the first criterion). The reference site was selected in the rocky mountain with similar environmental conditions. In addition, species which presented as particularly as high frequency and coverage of more than 60% on the abandoned coal mine spoils were selected as tolerant species additively (the second criterion) (Table 2).
As a result of the field survey, the most tolerant species were selected based on the first criterion rather than the second. This is because most plant species established naturally on the abandoned coal mine spoils showed very low coverage and frequency. In this respect, soil amelioration is urgently required to restore the coal mine area with more stability.

3.2. Selection of Tolerant Species by Cultivation Experiment in Laboratory

Initially, we planned to select species that grew in the control plot with coal mine debris larger than that in the experimental plot with ameliorated substrate as the tolerant species. However, there were no plants that showed such a response. Therefore, we compared the tolerance order of sample plants based on the ratios of growth coefficients of sample plants in the control plot with both plots ameliorated by applying organic fertilizer (OF) and forest soil (FS) (Table 3).
As a result of the comparison on the tolerance levels of 15 sample plants, trees of Pinus densiflora and Quercus mongolica showed the highest and the third highest tolerance order, respectively. Miscanthus sinensis showed the next highest tolerance, followed by Echinochloa, Themeda, Cymbopogon, etc. Overall, C4 plants showed higher tolerance order, legumes were the next, and C3 plants showed the lowest tolerance level.
Meanwhile, trees such as P. densiflora and Q. mongolica could not be compared directly with other sample plants because the measuring items were different from each other. However, compared based on the tolerance index obtained in this study, P. densiflora and Q. mongolica ranked first and third among the total sample plants, respectively. Compared with the two plants with the same life form, the tolerance of P. densiflora, which was the early successional species, was higher than Q. mongolica, the late successional species.

3.3. Soil Amelioration Effect

Soil amelioration effects were evaluated based on pH, OM, TN, AP, CEC, Ca, Mg, and K contents. The treatment of soil ameliorators showed significant differences among treatment plots with different supplies, such as non-treatment, OF 6.4 ton/ha, and OF 12.8 ton/ha plots (Figure 4). However, the evaluation results showed that the contents were lower compared with those of the reference sites, except for the organic matter content and nitrogen content of some plots.

3.4. Growth of Sample Plants

Plant growth showed significant differences among treatment plots with different amounts of soil ameliorators in all sample plants. From these results, the soil amelioration effect on the plant growth was identified from all sample plants (Figure 5).

3.5. Species Composition

The restoration site located in the lowlands consisted of an ecologically restored site, two afforested sites by introducing Betula schmidtii and Robinia pseudoacacia, and non-restored sites, respectively. As a result of stand ordination, the non-restored sites were located far from the reference sites and the restored and afforested sites, showing a large difference in species composition (Figure 6). The restored sites were located closer to the reference sites than the sites afforested through the introduction of Robinia pseudoacacia, along with the sites afforested through the introduction of Betula schmidtii on Axis I. Meanwhile, the restored sites were located closer to the reference sites than the sites afforested through the introduction of Betula schmidtii along with the sites afforested through the introduction of Robinia pseudoacacia on Axis II. Synthesizing the results, the restored sites tended to be located closer to the reference sites than the non-restored sites as well as the afforested sites; thus, it was judged that they had a more similar species composition to the reference sites.
As a result of stand ordination, compared with the lowland sites, the upland sites were located relatively close to each other, indicating that the difference in species composition between the sites was not large (Figure 7). However, the distance varied depending on the site. The restored sites tended to be located closer to the reference sites, along with the non-restored and sites afforested through the introduction of Betula platyphyla var. japonica than the sites afforested, through the introduction of Alnus incana subsp. hirsuta, Lespedeza cyrtobotrya, and Robinia pseudoacacia.

3.6. Species Diversity

In the restoration site located in the lowlands, the species diversity of each treatment site was compared with the reference site based on the species rank–dominance curves; species diversity of all treatment sites, including ecologically restored sites, was lower than that of the reference sites except, for the site afforested through the introduction of Robinia pseudoacacia (Figure 8). However, the restored site showed higher species diversity than the non-restored site.
In the restoration site located in the uplands, the species diversity of each treatment site was compared with the reference site based on the species rank–dominance curves; species diversity of all treatment sites, including ecological restored sites, was lower than that of the reference sites (Figure 9). However, even here, the restored site showed higher species diversity than the non-restored site.
Considering that the afforestation site had a stand age of more than 30 years, species diversity tended to increase in proportion to the time elapsed after restoration rather than the restoration method.

3.7. Evaluation Based on Exotic Species

Many exotic plants, including Ambrosia artemisiifolia var. elatior Desc., which the Korea Ministry of Environment has designated as a harmful plant disturbing the ecosystem, appeared in the restored coal mine spoils. Deliberately introduced species such as Robinia pseudoacacia, Pinus rigida Mill., Larix kaempferi Carrière., Amorpha fruticose L., Festuca arundinacea Schreb., Rudbeckia bicolor Nutt., and Trifolium pratense L. are included among them. However, there were more species that had naturally been established, represented by Ailanthus altissima Swingle., Ambrosia artemisiifolia var. elatior, Oenothera biennis L., Bidens frondosa L., Taraxacum officinale F.H. Wigg., etc. The percentage of exotic species was higher in all treatment sites than in reference sites, except for the non-restored site in the upland area (Figure 10). Comparing the exotic plant ratio between the restored and non-restored sites, there was no significant difference between both sites in both lowland and upland areas. However, in the upland area, the proportion of exotic plants in the restored site was considerably lower than that of the restored site. When comparing the ratio of exotic plants between the restored and afforested sites, the proportion of the former was higher in the lowland, but vice versa in the upland.

4. Discussion

4.1. Restoration Effects Based on Chemical Properties of Soil

Abiotic conditions in coal mine spoils are very similar to those of an early successional stage habitat. Coal mine debris excavated from deep mining does not function as soil by itself because it does not contain sufficient organic matter. Therefore, ecosystem development in these areas must progress in the same manner as primary succession: the process of ecosystem development on barren surfaces where severe disturbances have removed most vestiges of biological activity [4]. Succession progresses as a result of interactions between plants growing in a given area and their habitat and soil. The amelioration of soil by early colonizers facilitates the establishment of new species and promotes species compositional change to the next successional stage [2,3]. In this respect, soil amelioration is a preparatory stage which is necessary in the restoration of coal mine spoils.
Coal mine spoils generally comprise the bare stripped area, loose soil piles, waste rock and overburden surfaces, subsided land areas, and other land degraded by mining facilities, among which waste rocks often pose extreme stressful conditions for restoration. Mining disrupts the aesthetics of the landscape, and also disrupts soil components such as soil horizons and structure, soil microbe populations, and nutrient cycles that are crucial for sustaining a healthy ecosystem, hence resulting in the destruction of the existing vegetation and soil profile [59]. Overburdened dumps include adverse factors such as the elevated bioavailability of metals, elevated sand content, lack of moisture, increased compaction, relatively low organic matter content, and high surface temperature. Acidic dumps may release salt or contain sulfidic material, which can generate acid mine drainage [60]. The effects of mine wastes can be multiple, such as soil erosion, air and water pollution, toxicity, geo-environmental disasters, loss of biodiversity, and ultimately, a loss of ecosystem service [61,62].
It is imperative from the above that mineral extraction processes must ensure a return of productivity of the affected land. An increase in the concerns for environment has made concurrent post-mining reclamation of the degraded land as an integral feature of the whole mining spectrum [63]. Conservation and reclamation efforts to ensure the continued beneficial use of land resources are essential. Reclamation is the process by which derelict or highly degraded lands are returned to productive land, and by which some measures of biotic function and productivity are restored. Long-term mine spoil reclamation requires the establishment of stable nutrient cycles from plant growth and microbial processes [64,65,66]. Soil provides the foundation for this process; thus, its characteristics directly affect the future stability of the restored vegetation. The restoration of vegetation cover on overburden dumps can fulfill the objectives of stabilization, pollution control, visual improvement, and removal of threats to human beings [61]. Restoration strategies must address soil amelioration in order to return the land as closely as possible to its pristine condition and continue as a self-sustaining ecosystem. Therefore, adding additional organic matter to the soil in the early stages of reclamation would likely improve restoration success. In particular, organic fertilizer might be an excellent soil ameliorator because it contains high levels of available phosphorus as well as organic matter [67].
Soil amelioration usually represents a major challenge to most restoration programs [1,44,45,46]. In industrial areas, soil amelioration through the application of dolomite or sludge, a sort of organic fertilizer, contributes to successful restoration of the forest ecosystem degraded due to severe air and soil pollution through the neutralization of acidic soil, the enhancement of fertility, or reduction in Al3+ toxicity [1,20,67,68,69]. In this study, soil amelioration contributed to enhancement of the chemical properties of soil (Figure 4) and plant growth (Figure 5). However, the nutrient contents were lower compared with those of the reference sites (Figure 4). This might be because of possible differences in pedology of the sites and partly because we examined the soil properties in 0–10 cm soil depth, which might not represent the whole root zones of the trees. Thus, further investigations of the soil properties along the soil horizon need to be conducted to reach a better conclusion of the ameliorating effect of organic fertilizers.

4.2. Selection of Tolerant Plant Species

Restoration of a vegetation cover can contribute to stabilization, pollution control, visual improvement, and the removal of threats to human beings. Ecological restoration of loose mine spoil dumps is crucial to minimize their negative impact on the environment in the watershed and in downstream catchment areas. The introduction of vegetation for restoration stabilizes the spoil and expedites the pedogenic processes influencing soil properties [70]. Such reclamation efforts can significantly alter soil particle distribution, organic carbon, total nitrogen, available potassium, and cation exchangeable capacity of open pit mine fields [71]. Proper restoration can also reap ecosystem services because the restored mining site serves as a habitat for other species to establish, reduce soil erosion, and improve edaphic conditions [72,73].
However, the successful vegetation restoration of coal mine spoils and reconstruction of their ecosystem faces obstacles of loose materials devoid of soil, poor spoil fertility, high heavy metal content, and extreme acidity. The organic matter content of coal mine spoils is very low, some of which is mineralized organic carbon that cannot easily be absorbed by plants [74]. Soil nutrients are the main factors affecting the distribution and growth of vegetation [75]. In fact, nutrient deficiency is identified as a major restrictor of the successful restoration of ecosystems on coal mine spoils [76], in addition to soil moisture [77]. Mining destroys topsoil, making the physical structure of the soil substrate unsuitable for plant growth. Excessive heavy metals in the spoils hinder plant metabolism and stunt vegetation growth. Extreme pH values or soil salinization are detrimental to the initial colonization of vegetation on the spoil heaps [78]. The other factors impeding plant growth are poor capillary structure and lack of moisture in the coal mine spoils. Their large particle size is not conducive to retaining water, and causes moisture to be easily evaporated at a high temperature [73]. Without the soil structure prior to weathering, the level of cation exchange in the coal mine debris is rather low. When the cation exchange rate falls below 3%, the coal mine debris will have poor fertility and water retention capabilities [79]. A higher coal mine debris content in the spoils causes infiltration rates and saturated hydraulic conductivity to decrease [80].
Coal mine debris is only made up of minerals; thus, is not a true soil where minerals are mixed with organic matter. The substrate is deficient of nutrients, contains toxic substances, has significantly lower effects of soil microorganism and animal activities, and has many physical disabilities; thus, where it is reclaimed, the plant’s natural establishment progresses very slowly [81,82,83] and the plant’s growth is limited [84,85]. Environmental pollutants act as a selection pressure in the evolutionary process at the species level of plants, resulting in evolutionary changes. This evolutionary change may take millions of years or more, although can take place within several years or a generation or two [86,87,88]. For example, the resistance of plants to heavy metal contamination and herbicides is obtained within several years [88,89,90], and ongoing climate change has affected the ecological dynamics of many species and is expected to impose natural selection on ecologically important traits [91]. Additionally, in recent years, evidence of rapid evolution has been identified [92,93,94] thanks to the development of computing capabilities [95]. In addition, there are reports that rapid evolution is due to the spread of exotic species or contribute to the spread of exotic species [96,97].
Coal mining activities accompany the occurrence of coal mine debris, and these activities have a history of more than 100 years; therefore, tolerant species are expected to occur in the meantime. In order to quickly establish vegetation, the right species suitable for the coal mine spoils should be selected. The ultimate goal of this study was to recover the coal mine spoils to the forest of level similar to natural forest by introducing plants. The restoration work of coal mine spoils is likened to a primary succession without any vegetation; therefore, a restoration plan should be established by imitating the primary succession. To realize this goal, selecting tolerant plants that can withstand coal mine spoils is an essential process. The species for restoration is usually selected based on the following criteria [46]: (1) species to restore the function of ecosystems; (2) species that can eventually become members of the ecosystem; and (3) species that can ensure high biodiversity in the future and create a complete ecosystem with their own efforts. The tolerant plant species serves as an important foundation for successful restoration. Planting tolerant species not only has the effect of enduring poor coal mine waste and increasing the vegetation coverage, but can also create a natural landscape that matches the surrounding vegetation. In addition, it is possible to create an ecologically sound vegetation by inhibiting the invasion of exotic species [98]. From the results of field survey and experimental study, C4 plants and legumes were selected as plant species with higher tolerance level than C3 plants (Table 1 and Table 2); thus, we introduced Albizia julibrissin and Miscanthus sinensis var. purpurascens to our experimental restoration plot. C4 plants usually prefer a bare ground where they can receive enough sunlight and are tolerant to high temperature. It is believable that C4 plants showed higher tolerance due to their habitat preference and biological traits being more suited to the ecological condition of the coal mine spoils than C3 plants [99,100,101]. Legumes with a higher tolerance level next to C4 plants were judged to have a higher tolerance level compared with C3 plants that did not have such functions; they can exploit poor environmental conditions on their own by fixing atmospheric nitrogen. Selecting the tolerant plant species by classifying vegetation layers can contribute to restoring coal mine spoil sites into a multilayered forest. If the site is restored to multilayered vegetation rather than to simple existing afforestation, it can increase biodiversity [46,102,103].

4.3. Restoration Effects Based on Species Composition

The trajectory of a restoration project may be viewed in terms of ecosystem structure and function [104,105], both of which are impacted greatly by degradation. The fundamental goal of restoration is to return a particular habitat or ecosystem to a condition close to its pre-degraded state. Complete restoration would involve a return to that state, while a partial return, or other trajectories would result in rehabilitation or replacement with a different system [6,7,8,106,107,108]. To effectively restore degraded areas, or to protect existing high quality areas, we must be able to define the attributes of “normal”, undegraded (or “healthy”) habitats as a model [5,6,7,108,109]. One way of setting a baseline from which to measure restoration success is to define the normal “biological integrity” of a system and then measure deviations from there. Integrity implies an unimpaired condition or the quality or state of being complete or undivided. Biological integrity is defined as “the ability to support and maintain a balanced, integrated, adaptive biological system having the full range of elements and processes expected in the natural habitat of a region” [9,20,67]. To evaluate a restored ecosystem, the ecological attributes of the ecosystem are compared with those from an “undisturbed” reference [110,111,112,113]. In the present study, we compared the species composition of the restored sites with the natural reference vegetation, P. densiflora forest (lowland) and Q. mongolica forest (upland), and a plantation afforested by introducing several plant species such as Alnus incana subsp. hirsuta, Betula platyphylla var. japonica, Lespedeza cyrtobotrya, and Robinia pseudoacacia. In a restoration site located in a lowland area, the species composition of the restored site ecologically resembled the natural reference vegetation more closely than the non-restored sites as well as the sites afforested by introducing Robinia pseudoacacia (Figure 6). Even in a restoration site located in an upland area, the restored sites showed a higher similarity in species composition to the reference sites than the afforested or the non-restored sites (Figure 7). Therefore, the restorative treatment served to increase biological integrity and approached the restoration goal in both sites.

4.4. Effects of the Restorative Treatment on Species Diversity

The importance of biodiversity is based on diverse values that include various ecological functions that lead to environmental stability [114]. Biodiversity is reflective of the heterogeneity of a habitat or ecodiversity [115,116,117,118,119,120]. High biodiversity also is indicative of the integrity of an environment; a highly biodiverse ecosystem is healthy and well equipped with all of its necessary components [121,122].
The restoration effect in terms of biodiversity was not significant not only in comparison with the natural reference site, but also the afforested sites in both restoration sites located in lowland and upland areas (Figure 8 and Figure 9). The sites (R. pseudoacacia and A. incana subsp. hirsuta stands in lowland and upland areas, respectively) afforested many years ago showed higher biodiversity than the ecologically restored sites, although ecological considerations were not supported during the project. Considering that the afforestation site had a stand age of more than 30 years, whereas the ecologically restored sites has stand age of just 8 years, the difference may have been due to the time elapsed after restoration rather than the restoration method. In this respect, the restoration effect in terms of biodiversity needs to be monitored further in the future. In reality, species diversity in urban rivers and forests around industrial complexes tends to increase over time after restoration [1,20].

4.5. Evaluation Based on Exotic Species

Exotic plants can cause a variety of problems in native plant communities: excluding native species; altering the habitat, hydrology, and nutrient cycling; and greatly impacting plant and animal diversity [123,124,125,126,127]. Exotic species can transform the structure and species composition of ecosystems by repressing or excluding native species, either directly by out-competing them for resources or indirectly by changing the way nutrients are cycled through the ecosystem [124,126,128,129]. The increasing global prevalence of relatively few invasive species threatens to create a relatively homogenous planet rather than one characterized by its rich biological diversity and local distinctiveness [124,125,130,131,132]. Therefore, the invasion of alien organisms, a potentially lasting and pervasive imposition, is considered to be one of the main threats to biodiversity in the modern world [133,134,135,136,137]. Furthermore, the prevention and control of new invasions is a clear priority in emerging policies [124,128,138,139,140,141]. Disturbed lands are favorable microsites for exotic species equipped with opportunistic or ruderal life history strategies [13,14,15,17,124,125,142]. Sites disturbed severely or frequently, such as coal mine spoils, support many exotic species [143,144]. Successful, sustainable restoration practices are recommended to inhibit the invasion of exotic species [15,18,101]. Exotic species prefer open places that are not highly competitive. However, the restored sites of coal mine spoils take a long time for dense vegetation to be restored due to the poor ecological characteristics. In fact, this study has shown that both restored and afforested sites did not effectively exclude exotic plants; thus, the ratio of exotic plants was rather higher than that of the non-restored site in the upland area (Figure 10). In this regard, dense planting during restoration projects and protective planting to mitigate external effects are recommended [98,145].

5. Conclusions

Vegetation is difficult to establish in very barren and toxic places such as coal mine spoils. In order to ecologically restore these sites, the substrate must be improved to a level similar to normal soil. In addition, plants that are tolerant to such degraded environments should be selected and introduced. Furthermore, ecological restoration should be carried out reflecting the reference information obtained from intact natural vegetation of the corresponding area. In this study, restoration using a soil ameliorator not only improved the chemical properties of soil, but also significantly promoted the growth of planted species. In addition, ecological restoration brought about changes in the species composition of vegetation, but did not significantly increase species diversity or exclude the occurrence of exotic plants. As a whole, the restoration effort has brought some improvement, but more active interventions are still needed to increase the diversity of the restored forests and control of the spread of exotic species.

Author Contributions

Conceptualization, B.-S.L., A.-R.K. and J.S.; methodology, W.-S.O., J.-H.A., C.-H.L. and C.-S.L.; software, B.-S.L., A.-R.K. and J.S.; validation, A.-R.K., J.S. and C.-S.L.; formal analysis, B.-S.L., A.-R.K. and C.-H.L.; investigation, B.-S.L., A.-R.K., J.S., W.-S.O., J.-H.A., C.-H.L. and C.-S.L.; resources, C.-H.L. and C.-S.L.; data curation, B.-S.L. and J.S.; writing—original draft preparation, B.-S.L.; writing—review and editing, C.-S.L.; visualization, B.-S.L., A.-R.K. and J.S.; supervision, C.-S.L.; project administration, C.-S.L.; funding acquisition, C.-S.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Table A1. Chemical properties of organic fertilizer chosen as a soil ameliorator in this study.
Table A1. Chemical properties of organic fertilizer chosen as a soil ameliorator in this study.
Environmental FactorsContent
Water content (%)48.34
Organic matter (%)33.76
Total Nitrogen (%)1.24
Available Phosphorus (%)1.04
Exchangeable Potassium (%)0.26
C.E.C(cmol+/kg)35.0
Sodium (%)0.57

References

  1. Lee, C.S.; Moon, J.S.; Cho, Y.C. Effects of Soil Amelioration and Tree Planting on Restoration of an Air-Pollution Damaged Forest in South Korea. Water Air Soil Pollut. 2007, 179, 239–254. [Google Scholar] [CrossRef]
  2. Connell, J.H.; Slatyer, R.O. Mechanisms of succession in natural communities and their role in community stability and organization. Am. Nat. 1977, 111, 1119–1144. [Google Scholar] [CrossRef]
  3. van Andel, J.; Bakker, J.; Grootjans, A. Mechanisms of vegetation succession: A review of concepts and perspectives. Acta Bot. Neerl. 1993, 42, 413–433. [Google Scholar] [CrossRef]
  4. Walker, L.R.; Del Moral, R. Primary Succession and Ecosystem Rehabilitation; Cambridge University Press: Cambridge, UK, 2003. [Google Scholar]
  5. Society for Ecological Restoration International Science(SERI) and Policy Working Group(PWG). The SER International Primer on Ecological Restoration; Society for Ecological Restoration International: Washington, DC, USA, 2004. [Google Scholar]
  6. McDonald, T.; Gann, G.; Jonson, J.; Dixon, K. International Standards for the Practice of Ecological Restoration–Including Principles and Key Concepts; Society for Ecological Restoration: Washington, DC, USA, 2016. [Google Scholar]
  7. Gann, G.D.; McDonald, T.; Walder, B.; Aronson, J.; Nelson, C.R.; Jonson, J.; Hallett, J.G.; Eisenberg, C.; Guariguata, M.R.; Liu, J. International principles and standards for the practice of ecological restoration. Restor. Ecol. 2019, 27, S1–S46. [Google Scholar] [CrossRef] [Green Version]
  8. Bradshaw, A.D. Ecological principles and land reclamation practice. Landsc. Plan. 1984, 11, 35–48. [Google Scholar] [CrossRef]
  9. Karr, J.R. Ecological Integrity and Ecological Health Are Not the Same; National Academy Press: New York, NY, USA, 1996. [Google Scholar]
  10. Grove, R.H.; Burdon, J.J. Ecology of Biological Invasions; Cambridge University Press: Cambridge, UK, 1986. [Google Scholar]
  11. Hedgpeth, J.W. Foreign invaders. Science 1993, 261, 34. [Google Scholar] [CrossRef] [PubMed]
  12. Meffe, G.; Carroll, C.; Pimm, S. Community and ecosystem level conservation: Species interactions, disturbance regimes, and invading species. In Principles of Conservation Biology, 2nd ed.; Sinauer Associates, Inc. Pub.: Sunderland, UK, 1997; pp. 235–268. [Google Scholar]
  13. Johnstone, I.M. Plant invasion windows: A time-based classification of invasion potential. Biol. Rev. 1986, 61, 369–394. [Google Scholar] [CrossRef]
  14. Hobbs, R.J.; Huenneke, L.F. Disturbance, Diversity, and Invasion: Implications for Conservation. Conserv. Biol. 1992, 6, 324–337. [Google Scholar] [CrossRef] [Green Version]
  15. Lee, H.S.; Yoo, H.M.; Lee, C.S. Distribution pattern of white snakeroot as an invasive alien plant and restoration strategy to inhibit its expansion in Seoripool park, Seoul. Korean J. Biol. Sci. 2003, 7, 197–205. [Google Scholar] [CrossRef]
  16. International Union for Conservation of Nature (IUCN). IUCN Guidelines for the Prevention of Biodiversity Loss Due to Biological Invasion; SSC & ISSG: Gland, Switzerland, 2000. [Google Scholar]
  17. Lee, C.S.; Lee, K.S.; Hwangbo, J.K.; You, Y.H.; Kim, J.H. Selection of Tolerant Plants and Their Arrangement to Restore a Forest Ecosystem Damaged by Air Pollution. Water Air Soil Pollut. 2004, 156, 251–273. [Google Scholar] [CrossRef]
  18. Lee, H.W.; Lee, C.S. Environmental factors affecting establishment and expansion of the invasive alien species of tree of heaven (Ailanthus altissima) in Seoripool Park, Seoul. Integr. Biosci. 2006, 10, 27–40. [Google Scholar] [CrossRef]
  19. Ewel, J.J. Restoration is the ultimate test of ecological theory. In Restoration Ecology: A Synthetic Approach to Ecological Research; Cambridge University Press: Cambridge, UK, 1987; pp. 31–33. [Google Scholar]
  20. Lee, C.S.; Lee, H.; Kim, A.R.; Pi, J.H.; Bae, Y.J.; Choi, J.K.; Lee, W.S.; Moon, J.S. Ecological effects of daylighting and plant reintroduction to the Cheonggye Stream in Seoul, Korea. Ecol. Eng. 2020, 152, 105879. [Google Scholar] [CrossRef]
  21. Kondolf, G.M.; Micheli, E.R. Evaluating stream restoration projects. Environ. Manag. 1995, 19, 1–15. [Google Scholar] [CrossRef]
  22. Purcell, A.H.; Friedrich, C.; Resh, V.H. An Assessment of a Small Urban Stream Restoration Project in Northern California. Restor. Ecol. 2002, 10, 685–694. [Google Scholar] [CrossRef]
  23. An, J.H.; Lim, C.H.; Lim, Y.; Nam, K.B.; Lee, C.S. A review of restoration project evaluation and post management for ecological restoration of the river. J. Restor. Ecol. 2014, 4, 15–34. [Google Scholar]
  24. Nilsson, C.; Polvi, L.E.; Gardeström, J.; Hasselquist, E.M.; Lind, L.; Sarneel, J.M. Riparian and in-stream restoration of boreal streams and rivers: Success or failure? Ecohydrology 2015, 8, 753–764. [Google Scholar] [CrossRef]
  25. Lee, C.S. Role and task of restoration ecology in changing environment: Trends and issues in academic study, Biology. Natl. Acad. Sci. 2016, 5, 481–527. [Google Scholar]
  26. Paillex, A.; Schuwirth, N.; Lorenz, A.W.; Januschke, K.; Peter, A.; Reichert, P. Integrating and extending ecological river assessment: Concept and test with two restoration projects. Ecol. Indic. 2017, 72, 131–141. [Google Scholar] [CrossRef] [Green Version]
  27. Rubin, Z.; Kondolf, G.M.; Rios-Touma, B. Evaluating Stream Restoration Projects: What Do We Learn from Monitoring? Water 2017, 9, 174. [Google Scholar] [CrossRef] [Green Version]
  28. Suding, K.N. Toward an Era of Restoration in Ecology: Successes, Failures, and Opportunities Ahead. Annu. Rev. Ecol. Evol. Syst. 2011, 42, 465–487. [Google Scholar] [CrossRef] [Green Version]
  29. Kondolf, G.M. Five Elements for Effective Evaluation of Stream Restoration. Restor. Ecol. 1995, 3, 133–136. [Google Scholar] [CrossRef]
  30. Woolsey, S.; Capelli, F.; Gonser, T.O.M.; Hoehn, E.; Hostmann, M.; Junker, B.; Paetzold, A.; Roulier, C.; Schweizer, S.; Tiegs, S.D.; et al. A strategy to assess river restoration success. Freshw. Biol. 2007, 52, 752–769. [Google Scholar] [CrossRef]
  31. Weber, C.; Åberg, U.; Buijse, A.D.; Hughes, F.M.R.; McKie, B.G.; Piégay, H.; Roni, P.; Vollenweider, S.; Haertel-Borer, S. Goals and principles for programmatic river restoration monitoring and evaluation: Collaborative learning across multiple projects. WIREs Water 2018, 5, e1257. [Google Scholar] [CrossRef] [Green Version]
  32. Wortley, L.; Hero, J.-M.; Howes, M. Evaluating Ecological Restoration Success: A Review of the Literature. Restor. Ecol. 2013, 21, 537–543. [Google Scholar] [CrossRef]
  33. Hobbs, R.J.; Norton, D.A. Towards a Conceptual Framework for Restoration Ecology. Restor. Ecol. 1996, 4, 93–110. [Google Scholar] [CrossRef]
  34. Higgs, E.S. What is Good Ecological Restoration? ProEnviron. Promediu 1997, 11, 338–348. [Google Scholar] [CrossRef]
  35. Asbjornsen, H.; Brudvig, L.; Mabry, C.; Evans, C.; Karnitz, H. Defining reference information for restoring ecologically rare tallgrass oak savannas in the Midwestern United States. J. For. 2005, 103, 345–350. [Google Scholar]
  36. Thorpe, A.S.; Stanley, A.G. Determining appropriate goals for restoration of imperilled communities and species. J. Appl. Ecol. 2011, 48, 275–279. [Google Scholar] [CrossRef]
  37. Choi, Y.D. Theories for ecological restoration in changing environment: Toward ‘futuristic’restoration. Ecol. Res. 2004, 19, 75–81. [Google Scholar] [CrossRef]
  38. Fule, P.Z. Does it make sense to restore wildland fire in changing climate? Restor. Ecol. 2008, 16, 526–531. [Google Scholar] [CrossRef]
  39. Seabrook, L.; McAlpine, C.A.; Bowen, M.E. Restore, repair or reinvent: Options for sustainable landscapes in a changing climate. Landsc. Urban Plan. 2011, 100, 407–410. [Google Scholar] [CrossRef]
  40. Hull, R.B.; Gobster, P.H. Restoring Forest Ecosystems: The Human Dimension. J. For. 2000, 98, 32–36. [Google Scholar]
  41. Burke, S.M.; Mitchell, N. People as ecological participants in ecological restoration. Restor. Ecol. 2007, 15, 348–350. [Google Scholar] [CrossRef]
  42. Hobbs, R. Woodland restoration in Scotland: Ecology, history, culture, economics, politics and change. J. Environ. Manag. 2009, 90, 2857–2865. [Google Scholar] [CrossRef] [PubMed]
  43. Le, H.D.; Smith, C.; Herbohn, J.; Harrison, S. More than just trees: Assessing reforestation success in tropical developing countries. J. Rural. Stud. 2012, 28, 5–19. [Google Scholar] [CrossRef] [Green Version]
  44. Lee, C.S.; Cho, Y.C. Selection of Pollution-Tolerant Trees for Restoration of Degraded Forests and Evaluation of the Experimental Restoration Practices at the Ulsan Industrial Complex, Korea. In Ecology, Planning, and Management of Urban Forests: International Perspectives; Carreiro, M.M., Song, Y.-C., Wu, J., Eds.; Springer: New York, NY, USA, 2008; pp. 369–392. [Google Scholar]
  45. Bradshaw, A.D. The biology of land restoration. In Applied Population Biology; Jain, S.K., Botsford, L.W., Eds.; Springer: Dordrecht, The Netherlands, 1992; pp. 25–44. [Google Scholar]
  46. Dobson, A.P.; Bradshaw, A.D.; Baker, A.J.M. Hopes for the future: Restoration ecology and conservation biology. Science 1997, 277, 515–522. [Google Scholar] [CrossRef]
  47. Gunn, J.M. Restoration and Recovery of an Industrial Region: Progress in Restoring the Smelter-Damaged Landscape near Sudbury, Canada; Springer: Berlin/Heidelberg, Germany, 1995. [Google Scholar]
  48. Gunn, J.M. Restoring the Smelter-Damaged Landscape Near Sudbury, Canada. Restor. Manag. Notes 1996, 14, 129–136. [Google Scholar] [CrossRef]
  49. Jackson, M.L. Soil Chemical Analysis: Advanced Course; Prentice-Hall: New Delhi, India, 1967. [Google Scholar]
  50. Allen, S.E.; Grimshaw, H.M.; Rowland, A.P. Chemical analysis. Methods in plant Ecology; Moore, P.D., Chapman, S.B., Eds.; Blackwell: London, UK, 1986. [Google Scholar]
  51. Korea National Arboretum. Korean Plant Names Index. Available online: http://www.nature.go.kr/kbi/plant/pilbk/selectPlantPilbkGnrlList.do (accessed on 2 December 2021).
  52. Braun-Blanquet, J. Pflanzensoziologie: Grundzüge der Vegetationskunde, 3rd ed.; Springer: New York, NY, USA, 1964. [Google Scholar]
  53. Hill, M.O. Decorana. A Fortran program for detrended correspondence analysis and reciprocal averaging. Vegetatio 1979, 42, 47–58. [Google Scholar] [CrossRef]
  54. Magurran, A.E. Measuring Biological Diversity; Wiley-Blackwell: Hoboken, NJ, USA, 2004. [Google Scholar]
  55. Kent, M.; Coker, P. Vegetation Description and Analysis: A practical Approach; Wiley-Blackwell: Hoboken, NJ, USA, 1992. [Google Scholar]
  56. Lee, C.S.; You, Y.H.; Robinson, G.R. Secondary Succession and Natural Habitat Restoration in Abandoned Rice Fields of Central Korea. Restor. Ecol. 2002, 10, 306–314. [Google Scholar] [CrossRef]
  57. SAS Institute. PROC User’s Manual, 6th ed.; SAS Institute Inc.: Cary, NC, USA, 2001. [Google Scholar]
  58. Hill, M.O.; Gauch, H.G. Detrended Correspondence Analysis: An Improved Ordination Technique. In Classification and Ordination: Symposium on Advances in Vegetation Science, Nijmegen, The Netherlands, May 1979; van der Maarel, E., Ed.; Springer: Dordrecht, The Netherlands, 1980; pp. 47–58. [Google Scholar]
  59. Kundu, N.; Ghose, M. Soil profile characteristic in Rajmahal Coalfield area. Indian J. Soil Water Conserv. 1997, 25, 28–32. [Google Scholar]
  60. Ghose, M.K. Soil conservation for rehabilitation and revegetation of mine-degraded land. TERI Inf. Dig. Energy Environ. Entomol. 2005, 4, 137–150. [Google Scholar]
  61. Wong, M.H. Ecological restoration of mine degraded soils, with emphasis on metal contaminated soils. Chemosphere 2003, 50, 775–780. [Google Scholar] [CrossRef]
  62. Sheoran, A.; Sheoran, V.; Poonia, P. Rehabilitation of mine degraded land by metallophytes. Min. Eng. J. 2008, 10, 11–16. [Google Scholar]
  63. Ghose, M. Land reclamation and protection of environment from the effect of coal mining operation. Mine technology 1989, 10, 35–39. [Google Scholar]
  64. Singh, A.N.; Raghubanshi, A.S.; Singh, J.S. Plantations as a tool for mine spoil restoration. Curr. Sci. 2002, 82, 1436–1441. [Google Scholar]
  65. Lone, M.I.; He, Z.-l.; Stoffella, P.J.; Yang, X.-e. Phytoremediation of heavy metal polluted soils and water: Progresses and perspectives. J. Zhejiang Univ. Sci. B 2008, 9, 210–220. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Kavamura, V.N.; Esposito, E. Biotechnological strategies applied to the decontamination of soils polluted with heavy metals. Biotechnol. Adv. 2010, 28, 61–69. [Google Scholar] [CrossRef]
  67. Lee, C.S.; Cho, Y.C.; Shin, H.C.; Lee, S.M.; Lee, C.H.; Eom, A.H. An evaluation of the effects of rehabilitation practiced in the coal mining spoils in Korea 2:An Evaluation Based on the Physicochemical Properties of Soil. J. Ecol. Environ. 2008, 31, 23–29. [Google Scholar] [CrossRef]
  68. Kim, G.S.; Pee, J.H.; An, J.H.; Lim, C.H.; Lee, C.S. Selection of air pollution tolerant plants through the 20-years-long transplanting experiment in the Yeocheon industrial area, southern Korea. Anim. Cells Syst. 2015, 19, 208–215. [Google Scholar] [CrossRef] [Green Version]
  69. Kim, A.R.; Lim, B.S.; Seol, J.; Lim, C.H.; You, Y.H.; Lee, W.S.; Lee, C.S. Diagnostic Assessment and Restoration Plan for Damaged Forest around the Seokpo Zinc Smelter, Central Eastern Korea. Forests 2021, 12, 663. [Google Scholar] [CrossRef]
  70. Singh, P.; Ram, S.; Ghosh, A. Changes in physical properties of mine soils brought about by planting trees. Ecol. Environ. Conserv. Pap. 2015, 21, 187–193. [Google Scholar] [CrossRef]
  71. Zeng, L.; Zhou, L.; Guo, D.-L.; Fu, D.-H.; Xu, P.; Zeng, S.; Tang, Q.-D.; Chen, A.-L.; Chen, F.-Q.; Luo, Y.; et al. Ecological effects of dams, alien fish, and physiochemical environmental factors on homogeneity/heterogeneity of fish community in four tributaries of the Pearl River in China. Ecol. Evol. 2017, 7, 3904–3915. [Google Scholar] [CrossRef] [PubMed]
  72. Carter, C.T.; Ungar, I.A. Aboveground vegetation, seed bank and soil analysis of a 31-year-old forest restoration on coal mine spoil in southeastern Ohio. Am. Midl. Nat. 2002, 147, 44–59. [Google Scholar] [CrossRef]
  73. Oh, W.S.; Lee, C.S. Recovery of Ecosystem Service Functions through Ecological Restoration Practice: A Case Study of Coal Mine Spoils, Samcheok, Central Eastern Korea. Korean Soc. Environ. Biol. 2014, 32, 102–111. [Google Scholar] [CrossRef]
  74. Wei, Z.; Wang, Q. Research on limited factors of reclaimed soil in the large coal wastes Pile in fushun west opencast coal mine. Res. Soil Water Conserv. 2009, 16, 179–182. [Google Scholar]
  75. Zhang, Z.; Wang, J.; Zhang, J. Interaction between reclaimed soil and vegetation in mining area: A review. Soils 2018, 50, 239–247. [Google Scholar]
  76. Nussbaumer, Y.; Cole, M.A.; Offler, C.E.; Patrick, J.W. Identifying and ameliorating nutrient limitations to reconstructing a forest ecosystem on mined land. Science 2016, 24, 202–211. [Google Scholar] [CrossRef]
  77. Li, S.; Liber, K. Influence of different revegetation choices on plant community and soil development nine years after initial planting on a reclaimed coal gob pile in the Shanxi mining area, China. Sci. Total Environ. 2018, 618, 1314–1323. [Google Scholar] [CrossRef]
  78. Li, M.S. Ecological restoration of mineland with particular reference to the metalliferous mine wasteland in China: A review of research and practice. Sci. Total Environ. 2006, 357, 38–53. [Google Scholar] [CrossRef]
  79. Chen, J.; Liu, Z.; Wang, Z. Study on surface vegetation technology of waste rock mountain in Fuxin area. Opencast Min. Technol. 2005, 6, 46–48. [Google Scholar]
  80. Beibei, Z.; Ming’an, S.; Mingxia, W.; Quanjiu, W.; Horton, R. Effects of Coal Gangue Content on Water Movement and Solute Transport in a China Loess Plateau Soil. Clean–Soil Air Water 2010, 38, 1031–1038. [Google Scholar] [CrossRef]
  81. Down, C. Soil development on colliery waste tips in relation to age. I. Introduction and physical factors. J. Appl. Ecol. 1975, 12, 613–622. [Google Scholar]
  82. Down, C. Soil development on colliery waste tips in relation to age. Ⅲ. Chemical factors. J. Appl. Ecol. 1975, 12, 635–639. [Google Scholar] [CrossRef]
  83. Sheoran, V.; Sheoran, A.; Poonia, P. Soil reclamation of abandoned mine land by revegetation: A review. Int. J. Soil Sediment Water 2010, 3, 13. [Google Scholar]
  84. Lindemann, W.C.; Lindsey, D.L.; Fresquez, P.R. Amendment of Mine Spoil to Increase the Number and Activity of Microorganisms. Soil Sci. Soc. Am. J. 1984, 48, 574–578. [Google Scholar] [CrossRef]
  85. Simmons, J.A.; Currie, W.S.; Eshleman, K.N.; Kuers, K.; Monteleone, S.; Negley, T.L.; Pohlad, B.R.; Thomas, C.L. Forest to reclaimed mine land use change leads to altered ecosystem structure and function. Ecol. Appl. 2008, 18, 104–118. [Google Scholar] [CrossRef]
  86. Roose, S.P.; Glassman, A.H.; Walsh, B.T.; Cullen, K. Reversible Loss of Nocturnal Penile Tumescence during Depression: A Preliminary Report. Neuropsychobiology 1982, 8, 284–288. [Google Scholar] [CrossRef] [PubMed]
  87. Pitelka, L.F. Evolutionary responses of plants to anthropogenic pollutants. Trends Ecol. Evol. 1988, 3, 233–236. [Google Scholar] [CrossRef]
  88. Bradshaw, A.D.; McNeilly, T. Evolutionary response to global climatic change. Ann. Bot. 1991, 67, 5–14. [Google Scholar] [CrossRef]
  89. Antonovics, J.; Bradshaw, A.D.; Turner, R. Heavy metal tolerance in plants. In Advances in Ecological Research; Elsevier: Amsterdam, The Netherlands, 1971; Volume 7, pp. 1–85. [Google Scholar]
  90. Le Baron, H.M.; Gressel, J. Herbicide Resistance in Plants; John Wiley & Sons: Hoboken, NJ, USA, 1982. [Google Scholar]
  91. Franks, S.J.; Sim, S.; Weis, A.E. Rapid evolution of flowering time by an annual plant in response to a climate fluctuation. Proc. Natl. Acad. Sci. USA 2007, 104, 1278–1282. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  92. Ramos, S.E.; Schiestl, F.P. Rapid plant evolution driven by the interaction of pollination and herbivory. Science 2019, 364, 193–196. [Google Scholar] [CrossRef] [PubMed]
  93. Magnoli, S.M.; Lau, J.A. Novel plant–microbe interactions: Rapid evolution of a legume–rhizobium mutualism in restored prairies. J. Ecol. 2020, 108, 1241–1249. [Google Scholar] [CrossRef]
  94. Mackin, C.R.; Peña, J.F.; Blanco, M.A.; Balfour, N.J.; Castellanos, M.C. Rapid evolution of a floral trait following acquisition of novel pollinators. J. Ecol. 2021, 109, 2234–2246. [Google Scholar] [CrossRef]
  95. Smith, S.A.; Donoghue, M.J. Rates of Molecular Evolution Are Linked to Life History in Flowering Plants. Science 2008, 322, 86–89. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  96. Buswell, J.M.; Moles, A.T.; Hartley, S. Is rapid evolution common in introduced plant species? J. Ecol. 2011, 99, 214–224. [Google Scholar] [CrossRef]
  97. Vandepitte, K.; de Meyer, T.; Helsen, K.; van Acker, K.; Roldán-Ruiz, I.; Mergeay, J.; Honnay, O. Rapid genetic adaptation precedes the spread of an exotic plant species. Mol. Ecol. 2014, 23, 2157–2164. [Google Scholar] [CrossRef] [PubMed]
  98. Lee, C.S.; Cho, Y.C.; Shin, H.C.; Kim, G.S.; Pi, J.H. Control of an invasive alien species, Ambrosia trifida with restoration by introducing willows as a typical riparian vegetation. J. Ecol. Environ. Entomol. 2010, 33, 157–164. [Google Scholar] [CrossRef]
  99. Chang, N.K.; Lee, S.K. Studies on the Classification, Productivity and Distribution of C3, C4 and CAM Plants in Vegetations of Korea 1. C3 and C4 Type plants. Korean J. Ecol. 1983, 6, 62–69. [Google Scholar]
  100. Chang, N.K.; Lee, S.K. Studies on the Classification, Productivity, and Distribution of C3, C4 and CAM Plants in Vegetations of Korea 3. Production and Productivity of C3 and C4 Type Plants. Korean J. Ecol. 1983, 6, 114–127. [Google Scholar]
  101. Odum, E.P.; Barrett, G.W. Fundamentals of Ecology; Thomson Brooks/Cole: Belmont, CA, USA, 2005; Volume 3. [Google Scholar]
  102. Fox, J.F.; Campbell, J.E.; Acton, P.M. Carbon Sequestration by Reforesting Legacy Grasslands on Coal Mining Sites. Energies 2020, 13, 6340. [Google Scholar] [CrossRef]
  103. Moudrý, V.; Moudrá, L.; Barták, V.; Bejček, V.; Gdulová, K.; Hendrychová, M.; Moravec, D.; Musil, P.; Rocchini, D.; Šťastný, K.; et al. The role of the vegetation structure, primary productivity and senescence derived from airborne LiDAR and hyperspectral data for birds diversity and rarity on a restored site. Landsc. Urban Plan. 2021, 210, 104064. [Google Scholar] [CrossRef]
  104. Lake, P.S.; Bond, N.; Reich, P. Linking ecological theory with stream restoration. Freshw. Biol. 2007, 52, 597–615. [Google Scholar] [CrossRef]
  105. Hobbs, R.J.; Cramer, V.A. Restoration Ecology: Interventionist Approaches for Restoring and Maintaining Ecosystem Function in the Face of Rapid Environmental Change. Annu. Rev. Environ. Resour. 2008, 33, 39–61. [Google Scholar] [CrossRef]
  106. Bradshaw, A.D. Restoration: An Acid Test for Ecology; Cambridge University Press: Cambridge, UK, 1987. [Google Scholar]
  107. Aronson, J.; Floret, C.; Le Floc’h, E.; Ovalle, C.; Pontanier, R. Restoration and Rehabilitation of Degraded Ecosystems in Arid and Semi-Arid Lands. I. A View from the South. Restor. Ecol. 1993, 1, 8–17. [Google Scholar] [CrossRef]
  108. Kim, A.R.; Lim, B.S.; Seol, J.; Lee, C.S. Principle of restoration ecology reflected in the process creating the National Institute of Ecology. J. Ecol. Environ. 2021, 45, 12. [Google Scholar] [CrossRef]
  109. Lüderitz, V.; Jüpner, R.; Müller, S.; Feld, C.K. Renaturalization of streams and rivers—the special importance of integrated ecological methods in measurement of success. An example from Saxony-Anhalt (Germany). Limnologica 2004, 34, 249–263. [Google Scholar] [CrossRef] [Green Version]
  110. White, P.S.; Walker, J.L. Approximating Nature’s Variation: Selecting and Using Reference Information in Restoration Ecology. Restor. Ecol. 1997, 5, 338–349. [Google Scholar] [CrossRef] [Green Version]
  111. Rood, S.B.; Gourley, C.R.; Ammon, E.M.; Heki, L.G.; Klotz, J.R.; Morrison, M.L.; Mosley, D.; Scoppettone, G.G.; Swanson, S.; Wagner, P.L. Flows for Floodplain Forests: A Successful Riparian Restoration. BioScience 2003, 53, 647–656. [Google Scholar] [CrossRef]
  112. Whittier, T.R.; Stoddard, J.L.; Larsen, D.P.; Herlihy, A.T. Selecting reference sites for stream biological assessments: Best professional judgment or objective criteria. J. North Am. Benthol. Soc. 2007, 26, 349–360. [Google Scholar] [CrossRef]
  113. Gilvear, D.; Bryant, R. Analysis of remotely sensed data for fluvial geomorphology and river science. In Tools Fluvial Geomorphology; Kondolf, G.M., Piégay, H., Eds.; John Wiley & Sons Ltd.: Hoboken, NJ, USA, 2016; pp. 103–132. [Google Scholar]
  114. Naess, A. Ecology, Community and Lifestyle: Outline of an Ecosophy; Cambridge University Press: Cambridge, UK, 1990. [Google Scholar]
  115. Romme, W.H. Fire and Landscape Diversity in Subalpine Forests of Yellowstone National Park. Ecol. Monogr. 1982, 52, 199–221. [Google Scholar] [CrossRef]
  116. Haber, W. Using Landscape Ecology in Planning and Management. In Changing Landscapes: An Ecological Perspective; Zonneveld, I.S., Forman, R.T.T., Eds.; Springer: New York, NY, USA, 1990; pp. 217–232. [Google Scholar]
  117. Hoover, S.R.; Parker, A.J. Spatial components of biotic diversity in landscapes of Georgia, USA. Landsc. Ecol. 1991, 5, 125–136. [Google Scholar] [CrossRef]
  118. Naveh, Z. From Biodiversity to Ecodiversity: A Landscape-Ecology Approach to Conservation and Restoration. Restor. Ecol. 1994, 2, 180–189. [Google Scholar] [CrossRef]
  119. Lim, C.H.; Kim, G.S.; An, J.H.; You, B.H.; Bae, Y.S.; Byun, H.G.; Lee, C.S. Relationship between biodiversity and landscape structure in the Gyungan stream basin, central Korea. Entomol. Res. 2016, 46, 260–271. [Google Scholar] [CrossRef]
  120. An, J.H.; Lim, C.H.; Jung, S.H.; Kim, A.R.; Lee, C.S. Effects of climate change on biodiversity and measure for them. J. Wetl. Res. 2016, 18, 481–487. [Google Scholar]
  121. Meffe, G.; Carroll, C. Principles of Conservation Biology, 2nd ed.; Sinauer Associates Inc.: Sunderland, UK, 1997. [Google Scholar]
  122. Primack, R.B. A primer of Conservation Biology; Sinauer Associates Inc.: Sunderland, UK, 2008. [Google Scholar]
  123. Vitousek, P.M. Biological Invasions and Ecosystem Properties: Can Species Make a Difference? In Ecology of Biological Invasions of North America and Hawaii; Mooney, H.A., Drake, J.A., Eds.; Springer: New York, NY, USA, 1986; pp. 163–176. [Google Scholar]
  124. Mooney, H.A. Invasive alien species: The nature of the problem. In Invasive Alien Species: A New Synthesis; Island Press: Washington, DC, USA, 2005; Volume 63, pp. 1–15. [Google Scholar]
  125. Rawlins, K.; Griffin, J.; Moorhead, D.; Bargeron, C.; Evans, C. EDDMapS: Invasive Plant Mapping Handbook; Center for Invasive Species Ecosystem Health: Tifton, Georgia, USA, 2011. [Google Scholar]
  126. Jeschke, J.M.; Bacher, S.; Blackburn, T.M.; Dick, J.T.A.; Essl, F.; Evans, T.; Gaertner, M.; Hulme, P.E.; KÜHn, I.; MrugaŁA, A.; et al. Defining the Impact of Non-Native Species. Conserv. Biol. 2014, 28, 1188–1194. [Google Scholar] [CrossRef] [PubMed]
  127. Taylor, K.T.; Maxwell, B.D.; Pauchard, A.; Nuñez, M.A.; Rew, L.J. Native versus non-native invasions: Similarities and differences in the biodiversity impacts of Pinus contorta in introduced and native ranges. Divers. Distrib. 2016, 22, 578–588. [Google Scholar] [CrossRef] [Green Version]
  128. McNeely, J.A.; Mooney, H.A.; Neville, L.E.; Schei, P.J.; Waage, J.K. Global Strategy on Invasive Alien Species; IUCN: Cambridge, UK, 2001. [Google Scholar]
  129. McNeish, R.E.; McEwan, R.W. A review on the invasion ecology of Amur honeysuckle (Lonicera maackii, Caprifoliaceae) a case study of ecological impacts at multiple scales1. J. Torrey Bot. Soc. 2016, 143, 367–385. [Google Scholar] [CrossRef] [Green Version]
  130. Hobbs, R.J.; Mooney, H.A. Invasive species in a changing world: The interactions between global change and invasives. In Invasive Alien Species; Island Press: Washington, DC, USA, 2005; Volume 63, p. 310. [Google Scholar]
  131. World Health Organization(WHO). Connecting Global Priorities: Biodiversity and Human Health; WHO: Geneva, Switzerland, 2015. [Google Scholar]
  132. Milardi, M.; Gavioli, A.; Soininen, J.; Castaldelli, G. Exotic species invasions undermine regional functional diversity of freshwater fish. Sci. Rep. 2019, 9, 17921. [Google Scholar] [CrossRef] [PubMed]
  133. Werren, G.L. Environmental Weeds of the Wet Tropics Bioregion: Risk Assessment & Priority Ranking; Rainforest CRC: Cairns, QLD, Australia, 2001. [Google Scholar]
  134. Convention on Biological Diversity (CBD). Review of the Status and Trends of, and Major Threats to, Forest Biological Diversity; Secretariat of the Convention on Biological Diversity: Montreal, QC, Canada, 2002; p. 164.
  135. Zietsman, L. Observations on Environmental Change in South Africa; Africa SUN Media: Stellenbosch, South Africa, 2011. [Google Scholar]
  136. Agency, E.E. The Impacts of Invasive Alien Species in Europe; Publications Office of the European Union: Luxembourg, 2012. [Google Scholar]
  137. Early, R.; Bradley, B.A.; Dukes, J.S.; Lawler, J.J.; Olden, J.D.; Blumenthal, D.M.; Gonzalez, P.; Grosholz, E.D.; Ibañez, I.; Miller, L.P. Global threats from invasive alien species in the twenty-first century and national response capacities. Nat. Commun. 2016, 7, 12485. [Google Scholar] [CrossRef] [PubMed]
  138. Mack, R.N.; Simberloff, D.; Mark Lonsdale, W.; Evans, H.; Clout, M.; Bazzaz, F.A. Biotic invasions: Causes, epidemiology, global consequences, and control. Ecol. Appl. 2000, 10, 689–710. [Google Scholar] [CrossRef]
  139. Ruiz, G.M.; Carlton, J.T. Invasive species: Vectors management strategies. In Invasion Vectors: A Conceptual Framework for Management; Island Press: Washington, DC, USA, 2003; pp. 459–504. [Google Scholar]
  140. Dybas, C.L. Harmful algal blooms: Biosensors provide new ways of detecting and monitoring growing threat in coastal waters. BioScience 2003, 53, 918–923. [Google Scholar] [CrossRef] [Green Version]
  141. USDA, Natural Resources Conservation Services (NRCS). The PLANTS Database. 2013. Available online: https://www.nrcs.usda.gov/wps/portal/nrcs/main/national/plantsanimals/plants/ (accessed on 18 March 2022).
  142. Lázaro-Lobo, A.; Ervin, G.N. A global examination on the differential impacts of roadsides on native vs. exotic and weedy plant species. Glob. Ecol. Conserv. 2019, 17, e00555. [Google Scholar] [CrossRef]
  143. National Institute of Environmental Research (NIER). Survey for Ecological Impact by Naturalized Organisms (I); National Institute of Environmental: Seoul, Korea, 1995.
  144. National Institute of Environmental Research (NIER). Survey for Ecological Impact by Naturalized Organisms (II); National Institute of Environmental: Seoul, Korea, 1996.
  145. Zhou, T.; Liu, S.; Feng, Z.; Liu, G.; Gan, Q.; Peng, S. Use of exotic plants to control Spartina alterniflora invasion and promote mangrove restoration. Sci. Rep. 2015, 5, 12980. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. A map showing the study sites of the abandoned coal mine. Do indicates the administrative unit corresponding to the province. BP: Betula platyphylla var. japonica, RP: Robinia pseudoacacia, LC: Lespedeza cyrtobotrya, AI: Alnus incana subsp. hirsuta.
Figure 1. A map showing the study sites of the abandoned coal mine. Do indicates the administrative unit corresponding to the province. BP: Betula platyphylla var. japonica, RP: Robinia pseudoacacia, LC: Lespedeza cyrtobotrya, AI: Alnus incana subsp. hirsuta.
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Figure 2. A conceptual diagram of a restoration design that carried out soil improvement and vegetation introduction. The soil amelioration plots were composed of control plots with fresh coal mine debris, OF 6.4 plot ameliorated with the treatment of organic fertilizer of 6.4 ton/ha, and OF 12.8 plot ameliorated with the treatment of organic fertilizer of 12.8 ton/ha. In addition, natural forest soil was selected as the reference plot for comparison. The model for vegetation restoration in the lowland was prepared by imitating the Pinus densiflora forest as a reference site, and the upland was prepared by imitating the Quercus mongolica forest as a reference site. This diagram depicts one full replicate of the experimental design, with five replicates for the lowland site and three replicates for the upland site.
Figure 2. A conceptual diagram of a restoration design that carried out soil improvement and vegetation introduction. The soil amelioration plots were composed of control plots with fresh coal mine debris, OF 6.4 plot ameliorated with the treatment of organic fertilizer of 6.4 ton/ha, and OF 12.8 plot ameliorated with the treatment of organic fertilizer of 12.8 ton/ha. In addition, natural forest soil was selected as the reference plot for comparison. The model for vegetation restoration in the lowland was prepared by imitating the Pinus densiflora forest as a reference site, and the upland was prepared by imitating the Quercus mongolica forest as a reference site. This diagram depicts one full replicate of the experimental design, with five replicates for the lowland site and three replicates for the upland site.
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Figure 3. Restoration design prepared to realize true restoration in lowland (upper) and upland (lower) areas, by hypothesizing Pinus densiflora forest (upper) Quercus mongolica forest (lower) in the future. Pd: Pinus densiflora, Rm: Rhododendron mucronulatum Turcz., Lc: Lespedeza cyrtobotrya, Ms: Miscanthus sinensis, Ah: Arundinella hirta, Qm: Quercus mongolica, Bp: Betula platyphylla var. japonica, Bs: Betula schmidtii, Aj: Albizzia julibrissin, Sj: Styrax japonicus, Ap: Acer pseudosieboldianum, Rs: Rhododendron schlippenbachii, Ss: Spodiopogon sibiricus.
Figure 3. Restoration design prepared to realize true restoration in lowland (upper) and upland (lower) areas, by hypothesizing Pinus densiflora forest (upper) Quercus mongolica forest (lower) in the future. Pd: Pinus densiflora, Rm: Rhododendron mucronulatum Turcz., Lc: Lespedeza cyrtobotrya, Ms: Miscanthus sinensis, Ah: Arundinella hirta, Qm: Quercus mongolica, Bp: Betula platyphylla var. japonica, Bs: Betula schmidtii, Aj: Albizzia julibrissin, Sj: Styrax japonicus, Ap: Acer pseudosieboldianum, Rs: Rhododendron schlippenbachii, Ss: Spodiopogon sibiricus.
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Figure 4. Effect of organic fertilizer as a soil ameliorator on soil characteristics. Control: fresh coal mine debris plot, OF 6.4 ton: plot ameliorated treating organic fertilizer of 6.4 ton/ha, OF 12.8 ton: plot ameliorated treating organic fertilizer of 12.8 ton/ha, Reference: natural forest soil. Each bar is expressed as the mean and standard error of mean. Tukey’s honestly significant difference (HSD) test was conducted on each of the parameters that showed a statistically significant difference among the three types of treatments at α = 0.05; the means with the same alphabetical character (in superscript) for each parameter are not different from each other.
Figure 4. Effect of organic fertilizer as a soil ameliorator on soil characteristics. Control: fresh coal mine debris plot, OF 6.4 ton: plot ameliorated treating organic fertilizer of 6.4 ton/ha, OF 12.8 ton: plot ameliorated treating organic fertilizer of 12.8 ton/ha, Reference: natural forest soil. Each bar is expressed as the mean and standard error of mean. Tukey’s honestly significant difference (HSD) test was conducted on each of the parameters that showed a statistically significant difference among the three types of treatments at α = 0.05; the means with the same alphabetical character (in superscript) for each parameter are not different from each other.
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Figure 5. Height growth response of sample plants in control (fresh coal mine debris) and ameliorated plots (OF 6.4 ton and OF 12.8 ton). Control: fresh coal mine debris plot, OF 6.4 ton: plot ameliorated treating organic fertilizer of 6.4 ton/ha, OF 12.8 ton: plot ameliorated treating organic fertilizer of 12.8 ton/ha, Reference: natural forest soil. Each bar expresses the mean and standard error of the mean. Tukey’s honestly significant difference (HSD) test was conducted on each of the parameters that showed a statistically significant difference among the three types of treatments at α = 0.05; the means with the same alphabetical character (in superscript) for each parameter are not different from each other.
Figure 5. Height growth response of sample plants in control (fresh coal mine debris) and ameliorated plots (OF 6.4 ton and OF 12.8 ton). Control: fresh coal mine debris plot, OF 6.4 ton: plot ameliorated treating organic fertilizer of 6.4 ton/ha, OF 12.8 ton: plot ameliorated treating organic fertilizer of 12.8 ton/ha, Reference: natural forest soil. Each bar expresses the mean and standard error of the mean. Tukey’s honestly significant difference (HSD) test was conducted on each of the parameters that showed a statistically significant difference among the three types of treatments at α = 0.05; the means with the same alphabetical character (in superscript) for each parameter are not different from each other.
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Figure 6. DCA ordination of vegetation including sites restored ecologically (restoration), rehabilitated applying silvicultural method (Betula schmidtii and Robinia pseudoacacia), and reference stands dominated by Pinus densiflora.
Figure 6. DCA ordination of vegetation including sites restored ecologically (restoration), rehabilitated applying silvicultural method (Betula schmidtii and Robinia pseudoacacia), and reference stands dominated by Pinus densiflora.
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Figure 7. DCA ordination of vegetation including sites restored ecologically (restoration), rehabilitated applying silvicultural method (Alnus incana subsp. hirsuta, Betula platyphylla var. japonica, Lespedeza cyrtobotrya, and Robinia pseudoacacia), and reference stands dominated by Quercus mongolica.
Figure 7. DCA ordination of vegetation including sites restored ecologically (restoration), rehabilitated applying silvicultural method (Alnus incana subsp. hirsuta, Betula platyphylla var. japonica, Lespedeza cyrtobotrya, and Robinia pseudoacacia), and reference stands dominated by Quercus mongolica.
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Figure 8. Rank–abundance curves of vegetation including sites restored ecologically (restoration), rehabilitated applying silvicultural method (Betula schmidtii and Robinia pseudoacacia), and reference stands dominated by Pinus densiflora.
Figure 8. Rank–abundance curves of vegetation including sites restored ecologically (restoration), rehabilitated applying silvicultural method (Betula schmidtii and Robinia pseudoacacia), and reference stands dominated by Pinus densiflora.
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Figure 9. Rank–abundance curves of vegetation including sites restored ecologically (restoration), rehabilitated applying the silvicultural method (Alnus incana subsp. hirsuta, Betula platyphylla var. japonica, Lespedeza cyrtobotrya, and Robinia pseudoacacia), and reference stands dominated by Quercus mongolica.
Figure 9. Rank–abundance curves of vegetation including sites restored ecologically (restoration), rehabilitated applying the silvicultural method (Alnus incana subsp. hirsuta, Betula platyphylla var. japonica, Lespedeza cyrtobotrya, and Robinia pseudoacacia), and reference stands dominated by Quercus mongolica.
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Figure 10. A comparison of the percentage of exotic plants among the treatment sites including the reference site in restoration sites located inn lowland (left) and upland (right) areas, respectively. Each bar expresses the mean and standard error of mean. Tukey’s honestly significant difference (HSD) test was conducted on each of the parameters that showed a statistically significant difference among the three types of treatments at α = 0.05; the means with the same alphabetical character (in superscript) for each parameter were not different from each other.
Figure 10. A comparison of the percentage of exotic plants among the treatment sites including the reference site in restoration sites located inn lowland (left) and upland (right) areas, respectively. Each bar expresses the mean and standard error of mean. Tukey’s honestly significant difference (HSD) test was conducted on each of the parameters that showed a statistically significant difference among the three types of treatments at α = 0.05; the means with the same alphabetical character (in superscript) for each parameter were not different from each other.
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Table 1. The chemical properties of soil contained in pots prepared to select tolerant species in the laboratory experiment. Raw: coal mine debris, FS: ameliorated by adding forest soil on the coal mine debris, OF: ameliorated by adding organic fertilizer in the coal mine debris.
Table 1. The chemical properties of soil contained in pots prepared to select tolerant species in the laboratory experiment. Raw: coal mine debris, FS: ameliorated by adding forest soil on the coal mine debris, OF: ameliorated by adding organic fertilizer in the coal mine debris.
PlotpHOMTNAP (ppm)Ca2+Mg2+K
(%)(cmolc/kg)
Raw3.40 (0.08)7.85 (0.69)0.15 (0.02)0.02 (0.01)0.31 (0.04)0.12 (0.03)0.05 (0.03)
FS4.94 (0.06)7.93 (0.47)0.32 (0.03)6.96 (3.02)2.11 (0.04)0.75 (0.03)0.35 (0.04)
OF4.95 (0.10)16.1 (0.96)0.38 (0.03)2.15 (1.36)1.05 (0.06)0.48 (0.03)0.14 (0.03)
Numbers in parenthesis indicate standard deviations.
Table 2. Tolerant species selected by field survey in the abandoned coal mine spoils and nearby mountainous land with similar environmental condition.
Table 2. Tolerant species selected by field survey in the abandoned coal mine spoils and nearby mountainous land with similar environmental condition.
LayerSpeciesCriteria Rank
Canopy treePinus densiflora2
Quercus variabilis Blume.1
Q, mongolica1
Q. serrata Murray.1
Q. dentate Thunb.1
Betula davurica Pall.1
B. schmidtii2
B. platyphylla var. japonica2
Fraxinus rhynchophylla Hance.1
Kalopanax pictus Nakai.2
Understory treeLindera obtusiloba Blume.1
Maackia amurensis Rupr.1
Euonymus oxyphyllus Miq.1
Styrax obassia Siebold & Zucc.1
ShrubCorylus sieboldiana Blume.1
Fraxinus sieboldiana Blume.1
Juniperus rigida Siebold & Zucc.1
Lespedeza cyrtobotrya2
L. maximowiczii2
Rhododendron mucronulatum1
Rhus trichocarpa Miq.1
R. chinensis1
Salix hulteni Flod.2
Smilax china L.1
Tripterygium regelii Sprague & Takeda.1
Zanthoxylum schinifolium Siebold & Zucc.1
HerbSpodiopogon sibiricus2
Arundinella hirta2
Potentilla freyniana Bornm.1
Pteridium aquilinum var. latiusculum Underw.1
Vitis coignetiae Pulliat ex Planch.1
Miscanthus sinensis2
Themeda triandra var. japonica Forssk.1
Cymbopogon tortilis var. goeringii Hand.-Mazz.1
Echinochloa Crus-galli var. oryzicola Ohwi.1
Echinochloa crus-galli P.Beauv.1
Aster scaber Thunb.1
Actinidia rufa Siebold & Zucc.1
Polygonatum odoratum var. pluriflorum Ohwi.1
Saussurea grandifolia Maxim.1
Table 3. Growth coefficient in each plot, ratio of growth coefficient to the ameliorated plot, and the order of tolerance to the raw coal mine debris. Coal: raw coal mine debris plot, OF: plot ameliorated treating organic fertilizer of 12.8 ton/ha, FS: plot ameliorated covering forest soil of 10 cm depth.
Table 3. Growth coefficient in each plot, ratio of growth coefficient to the ameliorated plot, and the order of tolerance to the raw coal mine debris. Coal: raw coal mine debris plot, OF: plot ameliorated treating organic fertilizer of 12.8 ton/ha, FS: plot ameliorated covering forest soil of 10 cm depth.
Scientific Name
(Genus)
Coal OFFSCoal/OF (%)Coal/FS (%)Order of
Tolerance 1
Order of
Tolerance 2
Synthetic OrderRemarks
Pinus1.321.801.6073.382.5111Tree
Miscanthus0.550.940.7177.558.5142C4
Quercus1.001.501.4866.767.6223Tree
Echinochloa0.510.870.7964.658.6534C4
Themeda0.490.910.7169.053.8375C4
Cymbopogon0.330.600.5263.555.0656C4
Amaranthus0.230.420.3959.054.5767C4
Spodiopogon0.380.810.6855.846.9888C4
Lespedeza 10.270.590.4955.145.8999Legume
Melica0.310.720.5754.443.1101010C4
Lespedeza 20.270.650.5152.941.5111111Legume
Lespedeza 30.190.510.4349.337.3121212Legume
Albizzia0.230.650.4847.935.4131313Legume
Artemisia0.110.350.2839.331.4141414C3
Rumex0.120.520.3336.423.1151515C3
1 Order of tolerance of compared growth in substrate ameliorated by organic fertilizer. 2 Order of tolerance of compared growth in forest soil.
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Lim, B.-S.; Kim, A.-R.; Seol, J.; Oh, W.-S.; An, J.-H.; Lim, C.-H.; Lee, C.-S. Effects of Soil Amelioration and Vegetation Introduction on the Restoration of Abandoned Coal Mine Spoils in South Korea. Forests 2022, 13, 483. https://doi.org/10.3390/f13030483

AMA Style

Lim B-S, Kim A-R, Seol J, Oh W-S, An J-H, Lim C-H, Lee C-S. Effects of Soil Amelioration and Vegetation Introduction on the Restoration of Abandoned Coal Mine Spoils in South Korea. Forests. 2022; 13(3):483. https://doi.org/10.3390/f13030483

Chicago/Turabian Style

Lim, Bong-Soon, A-Reum Kim, Jaewon Seol, Woo-Seok Oh, Ji-Hong An, Chi-Hong Lim, and Chang-Seok Lee. 2022. "Effects of Soil Amelioration and Vegetation Introduction on the Restoration of Abandoned Coal Mine Spoils in South Korea" Forests 13, no. 3: 483. https://doi.org/10.3390/f13030483

APA Style

Lim, B. -S., Kim, A. -R., Seol, J., Oh, W. -S., An, J. -H., Lim, C. -H., & Lee, C. -S. (2022). Effects of Soil Amelioration and Vegetation Introduction on the Restoration of Abandoned Coal Mine Spoils in South Korea. Forests, 13(3), 483. https://doi.org/10.3390/f13030483

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