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Review

Prospects of Bioenergy Cropping Systems for A More Social-Ecologically Sound Bioeconomy

by
Moritz Von Cossel
1,*,
Moritz Wagner
1,
Jan Lask
1,
Elena Magenau
1,
Andrea Bauerle
1,
Viktoria Von Cossel
2,
Kirsten Warrach-Sagi
2,
Berien Elbersen
3,
Igor Staritsky
3,
Michiel Van Eupen
3,
Yasir Iqbal
4,
Nicolai David Jablonowski
5,6,
Stefan Happe
7,
Ana Luisa Fernando
8,
Danilo Scordia
9,
Salvatore Luciano Cosentino
9,
Volker Wulfmeyer
2,
Iris Lewandowski
1 and
Bastian Winkler
1
1
Biobased Products and Energy Crops (340b), Institute of Crop Science, University of Hohenheim, Fruwirthstr. 23, 70599 Stuttgart, Germany
2
Institute of Physics and Meteorology (120), University of Hohenheim, Garbenstr. 30, 70599 Stuttgart, Germany
3
Earth Informatics, Wageningen University and Research Centre, P.O. Box 47, 6700 AA Wageningen, The Netherlands
4
College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China
5
IBG-2: Plant Sciences, Institute of Bio- and Geosciences, Forschungszentrum Jülich, 52425 Jülich, Germany
6
Bioeconomy Science Center (BioSC), c/o Forschungszentrum Jülich, 52425 Jülich, Germany
7
Institute of Animal Breeding and Husbandry, Kiel University, Olshausenstr. 40, 24098 Kiel, Germany
8
MEtRICs, Departamento de Ciências e Tecnologia da Biomassa, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Campus de Caparica, 2829-516 Caparica, Portugal
9
Dipartimento di Agricoltura, Alimentazione e Ambiente (Di3A), University of Catania, 95123 Catania, Italy
*
Author to whom correspondence should be addressed.
Agronomy 2019, 9(10), 605; https://doi.org/10.3390/agronomy9100605
Submission received: 29 August 2019 / Revised: 29 September 2019 / Accepted: 30 September 2019 / Published: 2 October 2019
(This article belongs to the Special Issue Bioenergy Crops: Current Status and Future Prospects)

Abstract

:
The growing bioeconomy will require a greater supply of biomass in the future for both bioenergy and bio-based products. Today, many bioenergy cropping systems (BCS) are suboptimal due to either social-ecological threats or technical limitations. In addition, the competition for land between bioenergy-crop cultivation, food-crop cultivation, and biodiversity conservation is expected to increase as a result of both continuous world population growth and expected severe climate change effects. This study investigates how BCS can become more social-ecologically sustainable in future. It brings together expert opinions from the fields of agronomy, economics, meteorology, and geography. Potential solutions to the following five main requirements for a more holistically sustainable supply of biomass are summarized: (i) bioenergy-crop cultivation should provide a beneficial social-ecological contribution, such as an increase in both biodiversity and landscape aesthetics, (ii) bioenergy crops should be cultivated on marginal agricultural land so as not to compete with food-crop production, (iii) BCS need to be resilient in the face of projected severe climate change effects, (iv) BCS should foster rural development and support the vast number of small-scale family farmers, managing about 80% of agricultural land and natural resources globally, and (v) bioenergy-crop cultivation must be planned and implemented systematically, using holistic approaches. Further research activities and policy incentives should not only consider the economic potential of bioenergy-crop cultivation, but also aspects of biodiversity, soil fertility, and climate change adaptation specific to site conditions and the given social context. This will help to adapt existing agricultural systems in a changing world and foster the development of a more social-ecologically sustainable bioeconomy.

1. Introduction

At the 27th European Biomass Conference and Exhibition in Lisbon, there was a broad consensus that crop-based biomass is crucial for supporting a growing European bioeconomy [1]. Biomass from bioenergy crops is seen as a key element in the achievement of climate change mitigation strategies such as carbon sequestration and bioenergy with carbon capture and storage (BECCS) [2,3,4,5]. Today, most bioenergy crops are C3 and C4-plant species. Additionally, plant species with the crassulacean acid metabolism (CAM) such as the pencil tree (Euphorbia thirucalli L.) [6,7,8,9], prickly pear (Opuntia ficus-indica (L.) Mill. [10,11] and agave (Agave tequilana F.A.C.Weber) [12,13] have the potential for resilient bioenergy cropping systems (BCS) in drought-affected sites [14]—especially in the Mediterranean agroecological zone. However, crop-based bioenergy has stagnated over the last five years [1,15]. This is problematic in view of the EU’s ambition to reduce greenhouse gas (GHG) emissions by 40% by 2030 [16]. Of all renewable energies, biomass-based energy plays the most important role in power-to-X pathways [17], in particular, bio-based transportation fuels [18,19,20,21]. Together with electricity and hydrogen, biofuels are crucial for the decarbonization of the transport sector [18,19,21,22,23,24,25]. The use of bioenergy crops, crop residues, and organic civilization wastes as co-substrates in biogas plants could also be of significance in renewable energy production [26,27,28,29]. Further, bio digestion enables the efficient use of liquid manure for biogas production and, at the same time, the reduction of nitrous oxide emissions from manure [30,31], especially in organic farming systems [30,32]. However, there are various other utilization pathways for crop-based biomass beyond bioenergy, including biomaterials and biochemicals produced through biorefinery and cascading use concepts [33,34,35,36]. Increasing competition in biomass usage could have a negative impact on the bioenergy sector whenever it is more feasible to follow biorefinery or cascading use concepts than to simply produce bioenergy from biomass [33]. Increasing pressure on land use due to the food, energy, and environment trilemma [18,37,38,39,40,41,42,43] will further intensify competition between the production of industrially useable biomass for the growing bioeconomy and the rising demand for food and bioenergy. Thus, it remains unclear how bioenergy crops could significantly contribute to the achievement of the European Renewable Energy Directive II.
Consequently, when cultivating bioenergy crops, potentially adverse effects on food security need to be taken into consideration, on both a global and, in particular, local level [37,44,45]. This pressure on food security mainly applies to first-generation bioenergy crop cultivation on good arable soils [45,46,47,48,49,50]. As far as marginal agricultural land is concerned, the land use conflict with food crop cultivation is low [42,49,51,52,53,54]—indicating great bioenergy potential in these areas. Here, marginal agricultural land is defined as ‘lands having limitations which, in aggregate, are severe for the sustained application of a given use, and/or are sensitive to land degradation as a result of inappropriate human intervention, and/or have lost already part or all of their productive capacity as a result of inappropriate human intervention’ [55]. The limitations include a number of biophysical constraints such as adverse rooting conditions, contamination, and salinity [51]. Particularly because of the latter limitations, such sites are theoretically appropriate for biomass production because they are not suitable for food and feed production [56]. Worldwide, the estimated area of marginal agricultural land available for bioenergy crop cultivation amounts to approximately 7 Mm2 [57]. A high proportion of this area could be used for the cultivation of lignocellulosic bioenergy crops (providing second-generation biofuels) such as miscanthus (Miscanthus × giganteus Greef et Deuter), giant reed (Arundo donax L.), switchgrass (Panicum virgatum L.), as well as low-input high-diversity grasslands [58,59,60,61] and short rotation coppices among others. Therefore, these lignocellulosic bioenergy crops theoretically hold a high biomass potential [57]. However, there are many social and ecological challenges for the implementation of this theoretical biomass potential, especially with regard to the accessibility of marginal agricultural land as well as biodiversity concerns [62,63]. In addition, inadequate land use for bioenergy crop production carries the risk of increasing rather than decreasing GHG emissions [45] and altering climatic conditions at the micro to regional level, as has been seen in massive deforestation at the global level (e.g., palm oil plantations) [64]. Thus, the potential impacts of bioenergy crop cultivation on biodiversity [39,50,65] and societal conditions [66,67] must be carefully considered for any type of land—as is also the case in the food crop cultivation sector [42,68]. This leads to numerous fundamental challenges for the future of bioenergy crop cultivation, including (i) land use conflicts with food-crop cultivation [43], (ii) land use conflicts with biodiversity conservation [69,70], and (iii) the suitability for low-input cultivation (to keep environmental impacts low) on marginal agricultural lands [51,71]. While there are two general approaches to tackling the limitation of land—land sharing (wildlife-friendly farming) [70,72] and land sparing [72]—many questions remain with respect to more sustainable bioenergy crop cultivation in the future.
Against this backdrop, the objective of this study to assess the potential contribution of bioenergy crop cultivation for a more sustainable bioeconomy, reviewing both climate change effects and the associated social-ecological challenges.

2. Potential Contribution of Bioenergy Crop Cultivation in a Changing World

There is broad consensus among scientists on the fact that the cultivation of bioenergy crops must be in line with the sustainable development goals (SDGs) [1,43,73,74]. Therefore, future bioenergy crop cultivation should fulfill the following requirements:
(1)
Bioenergy crop cultivation should provide a beneficial social and ecological contribution, such as an increase of (agro-ecological) biodiversity and landscape aesthetics [58,75,76,77].
(2)
Bioenergy crops should be cultivated on marginal agricultural land and thus present no competition to food crop production. Therefore, bioenergy crops have to be able to cope with the given biophysical constraints on marginal agricultural lands [51,55,78,79].
(3)
Bioenergy cropping systems (BCS) need to be resilient towards the projected severe climate change effects [80,81,82,83].
(4)
These BCS should foster rural development and support the vast number of small-scale family farmers, managing about 80% of the global agricultural land and natural resources [84].
(5)
Accordingly, bioenergy crop cultivation must be planned and implemented systematically, and with the adoption of holistic approaches.
The following chapters describe how the potential BCS could fulfill these requirements.

2.1. The Potential Social-Ecological Contribution of Bioenergy Crop Cultivation

The utilization of marginal land is often linked to negative social-ecological impacts such as biodiversity losses, environmental pollution, and a decrease in the recreational value of the landscape [51,85]. This mainly applies to marginal forests and marginal high nature value areas (HNVs) which are accordingly considered unavailable for bioenergy crop cultivation. Conversely, the utilization of marginal agricultural land often promises to improve its overall value, or at least to maintain its current resilience and protect it from further degradation [55]. Many studies have revealed significant evidence to support the positive social-ecological effects of bioenergy crop cultivation on marginal agricultural land depending on the selected bioenergy crops and BCS, respectively [47,52,86,87,88,89,90]. Some dedicated bioenergy crops for cultivation on marginal agricultural land are shown in Figure 1. While some studies depict GHG emission savings [52,91], others have found that the best way of reducing GHG emissions and storing CO2 would be achievable through natural succession [92]. These and other relevant categories of social-ecological effects and impacts of bioenergy cropping will be discussed in the following sub-sections.

2.1.1. Bioenergy Crop Cultivation and Biodiversity

The task of protecting biodiversity has been acknowledged in the SDGs due to its central role in ecosystem functioning and human well-being [73,74]. According to the ‘Convention on Biological Diversity’ biological diversity is understood as the ‘variability among living organisms from all sources including, inter alia, terrestrial, marine and other aquatic ecosystems and the ecological complexes of which they are part; this includes diversity within species, between species and of ecosystems’ [93].
Bioenergy crop production influences biodiversity mainly through changes in land use (crop types and intensification) and land cover, which potentially result in habitat loss and fragmentation [93,94]. The large-scale deployment of bioenergy crops must therefore be carefully considered [95,96,97], which becomes apparent in the context of the wide-spread establishment of first generation bioenergy crops. There are clear indications that the intensive cultivation of annual energy crops such as maize or rape seed results in reduced species numbers due to a homogenization of landscape structures [95] (Figure 2). In comparison, results from small-scale and field-based studies have indicated that perennial bioenergy crops, such as miscanthus (Figure 1f), the cup plant (Silphium perfoliatum L.) (Figure 1d) [98], and willow (Salix spp.), provide positive, or at least less negative, impacts when compared with annual bioenergy crops [99,100,101,102]. However, the underlying implications for this are less obvious, and caution is required when making general assumptions. For instance, it has been shown that the impacts of the plantation of perennial crops may range from positive to even negative impacts on biodiversity compared to annual crops [97,103,104,105,106,107]. For example, miscanthus cultivation supports earthworm communities [89], but it does not provide nectar and pollen for pollinators as do wide crop rotations including flower-rich catch crops such as flax (Linum usitatissimum L.), lucerne (Medicago sativa L.) and Phacelia (Phacelia tanacetifolia Benth.) [108].
The variation in results is a general concern with respect to the assessment of biodiversity in agricultural landscapes. Comparisons of studies are often challenging as the results depend strongly on the surrounding context, including the previous land use and a wide range of simultaneously acting factors (e.g., crop management, yield levels, pathogens, and the presence of plant growth-promoting organisms) [109]. This includes time-dependency, which is a particularly important issue for perennial bioenergy crops, as species dynamics may vary over time (from planting years to finally productive periods). Furthermore, assessment approaches focus mainly on the field-scale and only a few taxonomic groups, while functional aspects of the community composition as well as landscape considerations are only slowly beginning to receive more attention. Overall, these arguments emphasize the need for further methodological improvement in the field of biodiversity assessment.
The above mentioned aspects are equally relevant if marginal agricultural lands are considered for a future biomass and bioenergy supply [110]. In addition, comprehensive analyses of the inherent biodiversity potential of these areas are needed in order to understand the conditions under which these areas can be used sustainably for bioenergy production [96]. However, it is to be kept in mind that bioenergy crop cultivation on marginal agricultural land does not only pose a risk to biodiversity, but can also serve conservation efforts in this regard [95,111]. For instance, the spread of rapidly proliferating species on abandoned land could be counteracted by the cultivation of weed-suppressing perennial plants such as miscanthus, giant reed, cup plant and Virginia mallow (Sida hermaphrodita L. Rusby).
Clearly, the effects of bioenergy crop cultivation also depend strongly on agricultural management, which underlines the importance of the implementation of better management practices for future bioenergy crop deployment [96]. Perennial bioenergy crops could be strategically planted in arable farmland in order to act as corridors to connect habitat fragments, to stimulate landscape heterogeneity, and to provide additional ecosystem services [102,112,113,114]. Examples of potential management options are the establishment of bioenergy buffers and the integration of perennial plants into conventional bioenergy production systems [113,115]. Following these and further approaches, present agricultural landscapes could be diversified in order to enhance biodiversity and supply sustainable energy.

2.1.2. Spatial and Temporal Diversification of BCS

Agricultural diversification, i.e., the spatial and temporal diversification of BCS, has been intensively investigated over the past centuries, mainly according to agro-ecological farming practices such as intercropping [116], agroforestry [117,118,119,120], and polycultures [121]. Species-rich meadows [59] or perennial wild plant mixtures [88,122] are promising approaches to increase both the spatial and temporal diversity of BCS for biomass and bioenergy supply [76,108,123,124]. However, there are numerous other diversification approaches which are less intense but still relevant in terms of their social-ecologically aspects. For bioenergy crop cultivation, these less intense crop diversification approaches include:
(1)
crop rotations [76,125,126,127,128],
(2)
the intercropping of annual or perennial crops with legumes [86,129,130,131,132],
(3)
the establishment of winter-annual species such as camelina (Camelina sativa L. Crantz) or perennial rye under annual crops [133,134,135], and
(4)
under maize-establishment of perennial energy crops such as miscanthus [115], the cup plant [136], and wild plant mixtures [122] among others [76,108,123].
Therefore, agricultural diversification is a basic approach for increasing agrobiodiversity. The main aims of increasing agrobiodiversity are (i) the support for both insects and open land animals [137,138,139,140,141] and (ii) the resilience of the agroecosystem and, as such, climate change adaptation. Additionally, well-conceptualized agricultural diversification can help to optimize the agronomic performance of the BCS [108]. There are numerous factors and mechanisms that determine the agronomic effects of agricultural diversification within and between the plant stands (Figure 3). Furthermore, physiological traits such as drought tolerance, pest resistance, and nitrogen (N) use efficiency are of great importance to the support for agrobiodiversity, for example, through higher biomass production and the avoidance of pesticide applications [5].
For bioenergy crop cultivation, agricultural diversification can be achieved by including additional crops into the BCS such as camelina [134,142,143] (Figure 1b), kenaf (Hibiscus cannabinus L.) [144], hemp (Cannabis sativa L.) [145] (Figure 1c), lupin (Lupinus mutabilis Sweet) [51,146], velvetleaf (Abutilon theophrasti Medic.), [147] biomass sorghum (Sorghum bicolor L. Moench) [148], willow [149,150], cup plant [122,151,152] (Figure 1d), amaranth (Amaranthus spp.) [129,153], yellow melilot (Melilotus officinalis L.) (Figure 1a), and woad (Isatis tinctoria L.) [122,131]—insofar as a certain level of growth suitability within the respective regions is given [51]. The higher the landscape heterogeneity, the better the overall ecological performance [108,154]. Further, the benefits are highly context-dependent, subject to both site- and region-specific aspects such as temporal and spatial habitat networking [155] and the given ecosystem conditions [156]. Moreover, some bioenergy crops can also contribute to more pollinator-friendly agriculture on marginal agricultural lands. This holds true for annual bioenergy crops such as camelina (Figure 1b) and crambe (Crambe abyssinica Hochst Ex Re Fries), because (i) they are not very demanding and suitable for several types of marginal agricultural land [51], and (ii) they produce nectar and pollen. Perennial flowering industrial crops such as cup plant, Virginia mallow (Figure 1e), willow and black locust (Robinia pseudoacacia L.) are even more promising due to their better environmental performance than annual crops [157,158,159]. However, the potential effects of perennial bioenergy crops on the existing agroecosystems should also be considered, especially in the case of neophytes such as the cup plant in Europe [151] and knapweed (Centaurea spp.) in the United States [160]. Since there is little knowledge of the effects of bioenergy cropping systems on pollinators on marginal agricultural land, further research is highly recommended.

2.1.3. Low-Input Agriculture, GHG Mitigation Potential and the Role of Legumes

Bioenergy crops cultivated under low-input agricultural practices [161,162] are of increasing importance in terms of emission reductions. Low-input agricultural practices can be applied in the categories (i) soil tillage, (ii) fertilization (mainly N and phosphorus (P)), (iii) fuel use, (iv) sowing material, and (v) plant protection measures. Once established, perennial bioenergy crops such as miscanthus, Virginia mallow, switchgrass, poplar (Populus spp.), and willow have a higher nutrient use efficiency than annual crops [163,164,165]. This is due to a better developed rooting system and the low demands of these crops for nutrients, water, and other inputs. The resilient nature of perennial bioenergy crops renders them highly relevant for a growing bioeconomy. This is because an efficient use and low amount of N fertilizer is required to significantly reduce agricultural GHG emissions because it reduces the requirements for N fertilizer production, as well as emissions from the soil [91,166,167,168,169,170].
For the outlined reasons and their potential to reduce N fertilizer requirements, the role of legumes and their capacity for atmospheric N fixation are also of great importance for sustainable biomass production and cropping strategies [87,132,171]. Some alternative bioenergy crops such as yellow melilot, lupin, and lucerne [88,108,122] are able to fix atmospheric N through rhizobacteria [132]. Thus, poor soils, such as marginal sandy substrates, can be enriched with non-synthetic N sources and increase the overall productivity of the agroecosystem in a natural way, for example, when intercropped with Virginia mallow as a perennial biomass plant [86]. In this case, a non-leguminous bioenergy crop potentially acts as a cover or catch crop, thus reducing N-leaching in surface and groundwater—as indicated by a recent study on a grain-legume cropping system [172]. However, legume intercropping with bioenergy crops may compete with soil resources—therefore, combining deep-rooting perennial crops and shallow-rooting legumes might be a promising option. Whereas, its practicability requires further validation. It is even possible to optimize legume-based N fixation through precision farming applications, for example, through mapping the field-level spatial variability for air–N fixation activity [173]. This could help to optimize the efficiency of other site-specific fertilization techniques, such as the application of solid manure or digestate. Consequently, the cultivation of legumes for bioenergy purposes will remain highly relevant to the pursuit of more social-ecologically sustainable bioenergy crop cultivation in future.

2.1.4. Groundwater Protection and Nutrient Recycling

The potential of groundwater protection for cropping systems can be explained roughly by its effect on the overall filtration capacity of the topsoil [174,175,176]. This means that the lower the nutrient leaching and the lower the use of synthetic agrochemicals such as herbicides, fungicides and insecticides, the lower the negative impact of the cropping system on the natural filtration capacity [174].
In Germany, there is a heated debate on when and where to apply how much manure or digestate after the winter period. This is because the manure or digestate tanks are full after winter, and thus need to be emptied quickly in spring. However, there are strict regulations for the maximum application rate (170 kg N ha−1 via organic fertilizers, following the German fertilizer ordinance of 2017) because the digestate contains considerable amounts of N (4.2 kg N m−3, [177]) and P (1.7 kg P m−3, [177]). Throughout Europe, the accumulation of manure in dense animal production regions results in a source to sink imbalance of nutrients which cannot always be compensated for via plant biomass production in situ. Consequently, the digestate must be transported over long distances to areas where nutrients are needed. This increases the transport costs and emissions [47,178]. Both of these challenges could be avoided because biogas cropping systems allow for improved on-farm nutrient cycling using separation and extraction techniques [179,180]. This means that it is possible to recover more than 90% of P from the digestates and transform it into fertilizable P-salt [179,181]. This P-salt can either be used as on-farm fertilizer for bioenergy (or food) crop cultivation, or it could be sold as a high value product [179]. After nutrient extraction, the remainder of the digestates have lower contents of N and P. This leads to practical advantages at the farm scale, because higher amounts of digestate can be applied at closer distances to the biogas plant without over-fertilizing, and without increasing the risk of nutrient leaching while the organic matter can still be used for maintaining or improving soil fertility [89].
Cultivating perennial bioenergy crops on marginal agricultural land will require sustainable fertilization strategies allowing for a successful establishment of the crops and a high biomass productivity, while avoiding nutrient leaching and potential aquifer pollution. For example, when cultivating Virginia mallow [182] in marginal sandy soil, digestate fertilization resulted in significantly less N leaching compared with NPK fertilizer but similar biomass yields and an increased soil carbon content, water holding capacity, and soil basal respiration, indicating an improved fertility of the marginal soil [132,183]. Other perennial biomass crops such as giant reed have the characteristic of leaving very low amounts of residual soil nitrate after harvest, which also helps in reducing potential N leaching over winter [184]. In an intercropping system of triticale and clover grass on two marginal sites, separated digestates were able to substitute mineral fertilizer completely in a long-term experiment (longer than six years) without decreasing biomass yield [185]. Moreover, wastewater reuse in the irrigation of perennial crops of giant reed and miscanthus was evaluated as an approach to promote bioenergy cropping systems in water-scarce regions (e.g., the Mediterranean) [186]. Results showed that biomass productivity was not affected and that the soil–plant system retained over 90% of the pollutant load, resulting in wastewater depuration. Additionally, many bioenergy crops, especially perennial crops [166,167,187], require low or even no chemical plant protection measures at all [51,88,122]. Thus, bioenergy crop cultivation on marginal soils, when cultivated with the aid of soil ameliorating biogenic residues used as fertilizers, could contribute to more sustainable biomass production and C storage in the future.

2.1.5. Soil Erosion Mitigation under Steep Slope Conditions

The prevention of soil erosion is a highly relevant issue, especially in the Mediterranean agro-ecological zone (AEZ) [51]. Generally, the risk of erosion is high when steep slope conditions are combined with low vegetative soil cover [188]. Under these conditions, both heavy rain and wind remove the topsoil layers which, over time, leads to a decrease in the rooting conditions. In the Mediterranean AEZ, an area of approximately 62,000 km2 is covered by sites prone to erosion and, in many cases, subject to further degradation [51,78]. Some wooden and perennial lignocellulosic bioenergy crops, such as miscanthus, giant reed, and other perennial grasses [60], provide the opportunity to cope with steep slope conditions and minimize soil erosion [188,189,190]. The strip cultivation of annual bioenergy crops can reduce soil erosion by up to 80% [190]—insofar as good agricultural practices are met. Such practices include the timing and type of soil tillage, because the lower the soil disturbance (i.e., minimum tillage, no tillage), the lower the erosion risk. In the Mediterranean area, soil tillage performed in early autumn is highly risky since the soil is not covered by vegetation and the bare soil is subjected to heavy rains, usually occurring from the end of summer. Furthermore, it is important to select both the right amount (and type) of fertilizer and the right time for its application according to each crop in erosion prone sites. In many cases, perennial bioenergy crops require low N and P applications because of their capability to relocate and re-use these nutrients [91,191].
Furthermore, perennial cropping systems can even increase the soil fertility of the erosion affected sites. This is because perennial cropping systems increase the living conditions for soil microbial communities [192], due to less soil disturbance (compared with annual cropping systems), soil organic carbon-enrichment [193], and a lower need for pesticides. This applies to most perennial bioenergy crops, such as miscanthus [163,194], switchgrass [60,195,196], giant reed [172] and willow [197,198]. Conversely, there is no information on the suitability of other perennial crops such as cup plant, Virginia mallow or wild plant species such as common tansy (Tanacetum vulgare L.), common knapweed (Centaurea nigra L.) and mugwort (Artemisia vulgaris L.) [88,122] for erosion prone sites with steep slope. Furthermore, steep slope conditions remain challenging for all agricultural, mechanized management procedures [199,200,201]. However, we assume that erosion affected sites could be economically and social-ecologically more sustainably utilized through perennial BCS compared with annual crops. In some cases, a terrace-like cropping system (following a basic agroforest approach under steep slope conditions) might enable a multiple use of the site for the simultaneous cultivation of both industrial and food crops [200].

2.2. The Potential Growth Suitability of Bioenergy Crops on Marginal Agricultural Lands

In total, European marginal agricultural land accounts for approximately 640,000 km2 [51] (Figure 4). The most severe constraint categories are (i) adverse rooting conditions (155,519 km2), (ii) adverse climatic conditions (112,096 km2), and (iii) excess soil moisture or poor drainage (108,081 km2) [51]. The following sub-sections highlight these major biophysical constraint categories of marginal agricultural land and how they could be overcome by adequate bioenergy crop cultivation.
Drought is very relevant for crop production as the amount and distribution of rainfall throughout the growing seasons affect plant growth, development, and yield. Limited amounts of water during plant growth causes water stress, in turn influencing physiological plant responses such as photosynthesis, mainly through stomatal closure to restrict water loss by transpiration [202,203,204]. Other typical symptoms of water stress include changes in cell growth, leaf expansion rate, and other plant morphological processes [202,205].
Soil moisture availability is a measure of dryness, which depends on the rates of precipitation and potential evapotranspiration. The combination of low precipitation and high evapotranspiration leads to poor crop growth by limiting the moisture supply. According to Van Orshoven et al. (2014) [206], dryness is calculated based on the ratio of annual precipitation (AP) to annual potential evapotranspiration (PET). The threshold value for dryness proposed by Joint Research Center (JRC) is 0.6 (AP/PET ≤ 0.6) [206,207].
Plants have developed different strategies to cope with drought, such as escape (typical of annual species), avoidance, and tolerance. These adaptive responses can contribute to a sustainable utilization of drought-prone marginal agricultural lands. Some perennial herbaceous grasses combine both avoidance and tolerance. Depending on the drought intensity, they can also apply adaptive responses including resistance to moderate drought with growth maintenance (dehydration avoidance and tolerance of lamina), growth cessation, and the survival of plants under severe stress to regrow at rehydration (dehydration avoidance and tolerance of meristems) [208].
The giant reed is one example of an opportunistic water using and drought resistant crop [60]. It is a mesophyte but can either grow in xeric or very humid environments. Efficient stomata regulation to contain water loss, leaf-rolling mechanism to increase the avoidance of dehydration by reducing incident radiation and temperature at the leaf level, and a deep root system explain the efficient water use and tolerance to durable periods of drought [202,209]. On the other hand, drought survival or summer dormancy is associated with some perennial pasture species of minor importance for bioenergy purposes, which however, could be valuable sources under extreme environments [210]. The annual bioenergy crop kenaf is also described as flexible in relation to water availability [211]. It reduces stomatal conductance and transpiration rate when water availability is limited, tolerating drought and being able to recover following re-watering.
Excess soil moisture conditions limit the oxygen supply in plant root zones impeding nutrient uptake [212]. Sub-optimal cultivation systems further increase the risk of disease outbreak and environmental damage through nutrient leaching, GHG emissions, and soil compaction. The mechanisms of both excess soil moisture and limited soil drainage have been concisely explained by Van Orshoven et al. (2014) [206]. Following their conclusions, excess soil moisture should be evaluated by adding up the number of days with soil moisture content exceeding field capacity [206]. The threshold for severe excess soil moisture conditions for plant growth is 230 days [206]. There are several known wooden and perennial bioenergy crops that can cope with severe excess soil moisture conditions, such as willow and reed canary grass [213].
Limited soil drainage is a morphometric parameter indicating soil wetness for a longer period. According to Terres et al. (2014) [207], an indicator for limited soil drainage is a Gleyic color pattern within 40 cm. Both excess soil moisture and limited soil drainage strongly depend on climate (e.g., high precipitation) and geophysical conditions, e.g., landscape and soil type. Under such conditions, perennial BCS, such as willow short rotation coppice, are suitable options [198]. Recently, several perennial crops were also found to be promising for waterlogged sites [214]. Whereas, these results draw on pot trials and need further evaluation under field conditions.
The cultivation of industrial crops in sites with high proportions of clay (>30%) [215] is promising because heavy clay is more or less unsuitable for the cultivation of food crops due to adverse rooting conditions [216]. This means that the potential for land use conflicts between industrial crop and food crop cultivation would be low. However, the cultivation of industrial crops on heavy clay soils is also challenging because of (i) a difficult establishment procedure, e.g., seed-bed preparation [217] (ii) and adverse rooting conditions, i.e., dry soil cracks and damage to the plant roots within the topsoil. This reduces the water and nutrient uptake ability of the plants. Consequently, the aspect of growing perennial industrial crops such as miscanthus [218] and giant reed [219] on marginal agricultural land affected by heavy clay should be further investigated.
Similarly challenging, and yet promising, is the cultivation of bioenergy crops in contaminated soils, especially for heavy metal contaminations [220,221]. Heavy metal contamination applies, if the contents of heavy metals, such as cadmium, zinc, and nickel, are above a certain threshold. In Europe, the Council Directive of 12 June 1986, identifies the limits for heavy metal concentrations in the soil [222]. These limits are meant to protect the environment, especially the soil, when sewage sludge is used in agriculture. The generic term for this type of marginal agricultural land is ‘adverse chemical conditions’ [51], and more than 22,500 km2 across Europe are affected [51]. Many bioenergy crops, such as miscanthus and giant reed [223], poplar trees [224], hemp, flax, and kenaf [225], have shown tolerance to heavy metal contamination. The cultivation of bioenergy crops in soils contaminated by heavy metals presents several opportunities. One positive social-ecological effect of utilizing contaminated land for BCS is the phytoremediation of the area: the presence of vegetation may improve soil properties, control soil erosion, and increase biological and landscape diversity and, after a certain period, the area could become available for food crop cultivation again [226]. Yet, yields can be affected by the contamination, as it was observed for sugar beet (Beta vulgaris L.) grown in nickel contaminated soils [227]. However, when the level of contamination in the soil is not high enough to induce toxicity, or when the existing contaminants are not bioavailable to be accumulated by the plants, yields may not be affected [228,229].
Furthermore, the accumulation of heavy metals within the biomass value chain (e.g., within the biogas value chain) must be avoided. This could be done by using another utilization pathway such as combustion [182,230,231]. For combustion, the heavy metal content will be highly concentrated within the ashes of the processed biomass. This contaminated ash can be disposed less problematically than contaminated digestate from biogas production, for example. However, the increment of ash material may increase the amount of fused agglomerates and slag deposits, accelerating the metal wastage of furnace and boilers components, thus reducing the equipment’s life [232]. Moreover, the yield loss may induce a concentration of elements such as N, increasing N oxide emissions if biomass is combusted [233]. A toolbox to address the technological and environmental constraints associated with the use of biomass for energy from marginal land has been prepared on the basis of current knowledge [234]. According to biomass composition, it is possible to choose the best energy technology for different types of contamination.

2.3. Climate Change Effects on Agriculture and Adaptation Strategies for Bioenergy Cropping Systems

This section reports on the projected climate change effects on agriculture [235], and how BCS could contribute to climate change adaptation with respect to low-input systems for biomass production in marginal agricultural land [51].

2.3.1. The Projected Climate Change Effects on Agriculture

Climate is one of the limiting factors for the growth of all plants including bioenergy crops. Growth degree days (GDD), annual precipitation, and drought events are key to determining whether a region is suitable for the cultivation of a certain bioenergy crop [51,206]. Therefore, an adequate estimation of the future growth suitability of bioenergy crops requires a consideration of climate change projections [236,237,238,239]. Regional climate model projections in the frame of the Coordinated Downscaling Experiment for Europe (EURO-CORDEX) [240] show significant warming and changes in precipitation in the 21st century. Notably, such changes depend on the radiation concentration pathway (RCP) and region (e.g., [241]). Results show a change in the precipitation statistics (amount, frequency, and intensity) causing more droughts, more wet periods, more rain instead of snow and a shift in the seasonal rainfall patterns in some regions (e.g. [242,243]). The length of the growing season will increase and change the crop’s phenological development pattern (crop-specific), thus increasing the vulnerability to late frost events, heat stress, and droughts. Within EURO-CORDEX, an ensemble of CMIP5 global climate model simulations is downscaled to ~ 12 km resolution with an ensemble of regional climate models. To reduce model uncertainty, these climate model ensemble data can be applied to force impact models [244]. For example, the projected change in GDD by the COSMO climate model (CCLM) downscaling the climate data from the EC-EARTH global climate model is displayed in Figure 5. Figure 6 shows the simulated change in precipitation for spring and autumn, which are relevant seasons for bioenergy crop cultivation.

2.3.2. The Potential Contribution of Bioenergy Cropping Systems to Climate Change Adaptation

Generally, the selection of the most suitable bioenergy crop for marginal agricultural land [51,52,82,245,246] will become even more relevant in terms of climate change adaptation, because severe changes in the basic climatic growth conditions are to be expected. This means that some bioenergy crops which are suitable for a certain area of marginal agricultural land today, e.g., contaminated soil, will not be suitable in the future, because the climatic growth conditions will become unsuitable. In large parts of France, Germany, and Hungary for example, there is a projected decrease of precipitation in spring and a projected increase of precipitation in autumn (Figure 6). Here, the rainfed growth conditions will become more challenging for annual bioenergy crops in the future, even though the annual precipitation shows no significant changes (not shown). This is because the changes of precipitation in spring (Figure 6a) affect the soil moisture conditions for the establishment procedures such as seedbed preparation and sowing of annual bioenergy crops. Changes of precipitation in autumn (Figure 6b) are relevant for the harvest management of those bioenergy crops harvested in autumn, such as maize, cup plant, biomass sorghum, and camelina. Most perennial BCS will be more promising than annual BCS in these regions in the light of climate change adaptation. This is because perennial BCS are less demanding in terms of soil tillage in the long term, and they can be harvested in winter when the topsoil is frozen, or at least less saturated than in the autumn. The opposite pattern (an increase of precipitation in spring and a decrease in autumn) is seen in Norway, eastern Italy, and Greece (Figure 6). Here, crop rotations with annual and biennial bioenergy crops may become more favorable in the future. Hence, it is to be expected that site-specific BCS may contribute to climate change adaptation on marginal agricultural land [51].
Furthermore, the projected increase of atmospheric CO2 of above 800 ppm by the end of the 21st century (RCP8.5) [80,247] is also expected to cause a great shift in the photosynthetic limitations of the bioenergy crops in terms of their photosynthetic pathways (C3, C4, CAM) [248,249]. This means that bioenergy crops with the C3-metabolism [51] are expected to become more relevant in warm regions than those bioenergy crops with the C4-metabolism [51], because the active CO2-assimilation of C4-metabolism [250] may become superfluous due to the expected increase of atmospheric CO2 concentrations [248,249]. However, the most important climate change effects to be addressed by well-adapted BCS will be the increased frequency and dimension of drought events [238,239,251].
Therefore, another climate change adaptation strategy that might be relevant for BCS on marginal agricultural land located in regions prone to increasing drought and heat events could be the use of agro-photovoltaic (APV) systems [252,253]. The idea is to shade the ground area with photovoltaic panels, which generate electricity and reduce the soil evaporation potential. A lower evaporation may lead to a higher soil moisture, and thus to a better water use efficiency by the bioenergy crops [252]. Consequently, both the erosion potential of, and the heat stress for bioenergy crops could be reduced underneath APV systems. However, the construction costs for APV systems are very high [252]. Therefore, which bioenergy cropping system to integrate to the APV system requires careful consideration. This is because the net-profit from both the electricity generated and the agricultural produce must compensate for the high construction costs of the APV system. Besides high-value crops, such as oil crops, perennial lignocellulosic crops could be suitable because their production costs are low—as far as low-input practices are considered [51,254]. Either way, both site-specific biophysical conditions and social-ecological requirements should also be taken into account to develop optimized APV system solutions. Thus, further thorough investigations of the effect of APV systems on the microclimate within the plant stands of BCS, in particular at the large scale, are highly recommended.
Additionally, BCS-related climate impacts should also be considered, since land use-change can affect local climate due to cropping-system-related changes in land surface albedo effects [255] or wind speed [256]:
(1)
Albedo effects could be induced by perennial BCS harvested in winter or spring, such as miscanthus and switchgrass, because the soil of these BCS is covered with senescence and thus brightly colored biomass during winter.
(2)
Wind speed can be reduced by perennial BCS with wooden crops such as agroforestry systems [117,118,257]—this helps to reduce wind erosion and increase the biomass yield [256].
Crop diversification, by means of implementing (perennial) bioenergy crops into existing farming systems, is also a relevant strategy for small-scale family farmers in countries of the south to (i) adapt to climate change and (ii) improve access to modern and clean energy, and thus (iii) improve living conditions.

2.4. Fostering Rural Development and Sustainable Rural Livelihoods

Decentralized bioenergy production is a major driver for increasing access to modern, clean, and affordable energy, in particular in rural areas in countries of the south [22,66,258,259,260]. In these areas, almost 1 billion people lack access to electricity, while 2.7 billion rely on traditional biomass (e.g., firewood), kerosene, or coal for cooking [22].
The Food and Agriculture Organization of the United Nations regards the integration of renewable energy production into rural smallholder farming systems as vital for the provision and sustenance of rural livelihoods and the sustainable improvement of agricultural production systems [261]. ‘Integrated Food and Energy Systems’ (IFESs) are based on the principles of sustainable production intensification [261]. Agricultural productivity is maximized through high agrobiodiversity while maintaining the productive capacity of the overall land-use system. Among renewable energy technologies (RET), biodigestion has the advantage that, in addition to energy production, it can help to close nutrient cycles in agricultural systems. An example of an IFES is the ‘livestock-biogas-fruit system’ developed in Guangdong, South China [262]. Orchard residues and pig manure form the feedstock for biodigesters located under the pig stables. The digester provides biogas as a clean energy source and organic fertilizer. The latter, in turn, improves soil fertility and reduces mineral fertilizer inputs. Further, chickens roam in the orchards, feeding on weeds and pests, decreasing pesticide application and, additionally, providing manure for biodigestion [262].
China is a country with an increasing number of biogas plants. The roll-out of decentralized biogas production started more than a century ago with the aim of increasing energy security in rural areas. The development peaked during the 1970s and resulted in the installation of about 43 million digesters by 2013 [263]. Today, Chinese energy development policies still focus on biodigestion. The aim is to increase biogas production from 16 Gm3 in 2013 to 44 Gm3 by 2020, also including centralized large-scale biodigesters [263]. India followed from the 1980s onwards with the National Biogas and Manure Management Programme, leading to the successful installation of 4.75 million biodigesters by 2014 [264] (Figure 7).
The planning and implementation of best–adapted marginal agricultural land low-input systems (MALLIS) need to take local communities, household needs, people’s assets, as well as the local natural resource base into account [51]. In addition to technical feasibility and economic performance, locally relevant social aspects need to be considered [66], including: acceptance and trust of new technologies and cropping systems; participation in planning and decision making [265]; gender relations; levels of education, skills and knowledge [266]; poverty level; food and nutrition security [258]; access to clean water [267]; land-use patterns [268], and work load [269].
The ‘Integrated Renewable Energy Potential Assessment’ (IREPA) approach provides a holistic and participatory tool for assessing the local appropriateness of bioenergy technologies and designing the respective bioenergy crop cultivation system [66]. With IREPA, the local renewable resource base and people’s livelihoods are explored. Based on that, RET are planned according to the available resource base and the role of energy in people’s (farming) lives [66]. The application of IREPA identified household biodigesters among the most appropriate options for implementation in a rural community in South Africa and two rural villages in India [66,260]. The major benefit expressed by the interviewed farmers is the ability of a biodigester to produce energy and fertilizer at the same time. The farmers in the Indian case study could not afford mineral fertilizers and had to improve soil fertility by increasing soil organic matter content after decades of intensive production [260], while farmers in South Africa had very limited access to mineral fertilizer due to affordability constraints and poor infrastructure [66].
Bioenergy-based MALLIS [51] are a promising option for the creation of regenerative agricultural systems. Biodigestion is an incentive for farmers, in particular in countries of the South, to collect biomass (including dedicated bioenergy crops, agricultural residues, weeds, organic household wastes, animal manure, and human feces), channel it into the digester to obtain biogas, and to bring the ‘digested biomass’ back to their fields as organic fertilizer. Closing natural resource cycles on a local level, and thus mimicking natural processes, is a major driver for the sustainable intensification of agriculture which, in turn, fosters the creation of sustainable livelihoods [32].
Furthermore, circular agricultural production systems are also very suitable for urban farming. In cities, huge amounts of organic waste are created, offering enormous potential for urban food production. A very elaborate example is the ‘Food-to-waste-food’ system of Stoknes et al. 2016 [270] whereby edible mushrooms and vegetables are nourished solely by organic wastes, treated through vermicomposting and biodigestion in a bubble-insulated greenhouse. This novel circular food system showed that organic waste provides enough energy for the operation of the greenhouse (light, heat, pumps, etc.) and, at the same time, sufficient amounts of nutrients for intensive vegetable production [270] in urban environments.
Consequently, biodigestion is a key technology for circular agricultural production systems, in rural as well as urban areas. The major advantage of this technology is the decentralized production of valuable fertilizer by channeling organic waste streams into the digester and, from there, back into the agricultural system. The biogas produced is just a by-product—albeit very valuable.

3. Chances and Challenges for a More Holistic Evaluation of Bioenergy Cropping Systems

Many opportunities and strategies are presented above that are expected to enable more social-ecologically benign and yet productive bioenergy crop cultivation. This is required to contribute to a growing bioeconomy without impeding any SDG in the future. However, in order to guarantee this, a holistic ex ante evaluation of the sustainability of various BCS is indispensable. Hereby, not only the environmental performance of the respective BCS must be taken into account, but also the positive and negative socio-economic impacts on the region. The Life Cycle Assessment (LCA) technique is an internationally recognized methodology to assess the environmental impacts of products or services over their whole life-cycle [271]. The LCA methodology is widely used to analyze the environmental performance of various BCSs on marginal land, such as miscanthus, giant reed, switchgrass, or cardoon [24,272,273,274,275]. The results of these studies demonstrated, that the use of perennial crops often shows a more favorable environmental performance compared to conventional annual bioenergy crops and in several impact categories also compared to a fossil reference [52,91]. However, even though LCA is widely used, several aspects are still missing, which would be of particular importance for the assessment of the BCSs on marginal land discussed in the current study. Herewith, especially soil quality [276] and the impact of different agricultural systems on the biodiversity [277] are crucial aspects that are not fully included in the current methodologies. In addition, it is crucial to assess whole crop rotations, however, currently, often only the environmental performance of individual crops is analyzed [278]. This is especially true for the BCS which include intercropping and the use of legumes.
As mentioned above, besides environmental considerations, economic aspects also play a major role in the holistic evaluation of different bioenergy crops. Many studies, which compare the economic performance of bioenergy and fossil energy sources, have only assessed the direct costs, excluding externalities. As a consequence, the costs of fossil products are often underestimated, whereas those of biobased alternatives are overestimated. One example of such an externality is the emission of CO2. In the European Union, the price per European Emission Allowances currently stands at around 29 € t−1 CO2 [279]. However, the German Environment Agency (UBA) estimates the real environmental costs per ton of CO2 at around 180 Euro [280]. This constitutes an immense indirect subsidy for emission-heavy industries, such as that of fossil-based energy generation. Another example would be ecological services, such as pollination, which positively correlate with both crop diversity and perennialism [139,281]. Pollination for example is a very important ecosystem service with a significant economic impact [282]. Several perennials such as wild plant mixtures have a positive influence on pollinator populations [283]—however this impact is not accounted for on an economic basis. This emphasizes the importance of the integration of environmental and economic aspects. Therefore, either the environmental impacts have to be monetized and thus internalized [284] or a combined assessment of the economic and environmental performance have to take place. In recent years, more assessments have come to include, as well as an environmental assessment, an economic evaluation of the BCS under study [52,285] in order to provide a more holistic picture. In addition to the economic aspect of the introduction of novel BCSs, social aspects must be included. For example, the landscape aesthetics of different BCSs have a significant impact on the acceptance of different stakeholder groups [286].
Consequently, it is crucial to analyze the socio-economic performance of these novel BCSs in addition to the environmental performance before their application on marginal land. One technique to evaluate the economic, social and environmental performance of the various BCSs holistically is the life-cycle sustainability assessment (LCSA) approach [287]. In the framework of an LCSA a Life Cycle Assessment (LCA) is conducted to assess the environmental impacts, and a life cycle costing (LCC) approach is used to evaluate the economic performance. The social impacts on various stakeholders are assessed by applying a social life cycle assessment (SLCA) [287].

4. Conclusions

Bioenergy cropping systems provide a number of promising options for a growing bioeconomy, under the premise that site-specific social-ecological factors are carefully taken into account during planning and implementation phase and in agronomic management. Aspects that need to be considered at the planning stage of BCS include: previous or alternative land use, field size, duration of cultivation (annual, perennial), agronomic practices (e.g., timing and type of soil tillage, amounts of fertilizer and pesticides), and crop-specific characteristics such as the depth of the root system, water and nutrient use efficiency, and its ability to cope with biophysical constraints.
The conversion from annual to perennial bioenergy crops tends to be advantageous for biodiversity and soil fertility. Perennial crop cultivation in corridors in between fields connects habitats, increases landscape heterogeneity and thus fosters the provision of ecosystem services. Intercropping, polyculture and agroforestry also increase agrobiodiversity by cultivating bioenergy crops in combination with food or fodder crops.
Further, perennial bioenergy crops that require low levels of agricultural inputs (tillage, fertilization, and plant protection) are preferential. Examples of perennial crops with relatively low demands and high nutrient-use efficiency include miscanthus, switchgrass, giant reed, Virginia mallow, common tansy, common knapweed, mugwort, poplar, willow, and black locust. The latter is a leguminous bioenergy crop that fixes atmospheric N through bacterial activity and can naturally improve the productivity and efficiency of the overall BCS. Intercropping diverse perennial BCS with legumes also offers the opportunity to reduce N leaching into surface and groundwater bodies which, for example, also supports compliance with the EU water framework directive. In addition, BCS on slopes reduce soil erosion, and thus nutrient losses.
Moreover, biogas cropping systems can improve on-farm nutrient cycling. Modern separation and extraction techniques enable P-salt recovery from biogas digestate, providing relief from nutrient surpluses, especially in regions of dense animal production. As biogas digestate has considerably lower P and N contents after P-salt recovery, larger amounts of the digestate can be applied on-farm, thus reducing the transport of this organic fertilizer with relatively low nutrient concentrations to other areas.
The establishment of BCS on marginal agricultural land reduces competition with the continuously growing demand for food production. For example, soils with a clay content exceeding 30% are often considered unsuitable for annual food crops, due to adverse rooting conditions for the crop and adverse management conditions for the farmer (inaccessible for machinery when wet and untillable when dry). On marginal agricultural land however, bioenergy crops that are able to cope with the given biophysical constraints need to be selected. For instance, willow is suitable in areas with (periodic) water logging, while giant reed is suitable for areas that are periodically waterlogged and at the same time drought prone. BCS are also potentially suitable for the phytoremediation of contaminated soil. Crops dedicated to combustion may take up heavy metals. These metals become concentrated in the ash at a later stage and can be disposed of safely.
The careful selection of bioenergy crops becomes even more relevant in view of the projected effects of climate change. The winter harvest of perennial bioenergy crops is an agronomic advantage in regions with a predicted increase in precipitation in autumn, the harvest period of many annual bioenergy crops. Perennial bioenergy crops with better established root systems tend to be preferential in areas becoming more prone to drought. In such regions, another promising option is the shading of crops to reduce soil evaporation, e.g., by intercropping herbaceous species with woody species to establish agroforestry BCS. Agro-photovoltaic systems are also suitable for the shading of crops and soils and have the advantage of decentralized electricity generation.
Decentralized energy production provides an additional or alternative income source for farmers in rural areas. In countries of the South, integrated food and energy production systems offer rural areas increased access to modern, clean, and affordable energy. The governments of India, and in particular China, have been advocating household biodigesters as a rural energy source for decades. This provides a major incentive for farmers to channel organic residues, wastes, and manure through the biodigester to obtain both biogas as an energy source and organic fertilizer for their agricultural fields. In these areas, bioenergy can accelerate the creation of circular integrated food and energy systems with a high crop diversity, productivity and efficiency.
The careful integration of the site-specific selection of perennial bioenergy crops can diversify and hence support agricultural farming systems worldwide by: (i) increasing biodiversity and thus ecosystem services, (ii) improving soil fertility, nutrient cycling, and thus productivity, (iii) enabling productive utilization (and restoration) of marginal land areas, (iv) creating additional income and supporting income diversification in rural areas, (v) increasing access to modern, clean and affordable energy, and (vi) aiding resilience and climate change adaptation.
In light of this, it is highly recommended that both further research activities (e.g., biomass potential analysis, implementation, and cultivation guidelines) and policy incentives (e.g., subsidies and greening measures) should not only consider the economic potential of bioenergy crop cultivation, but also aspects of biodiversity, soil fertility, and climate change adaptation, specific to the site conditions and given social context at the local to regional scale. A strong interdisciplinary network of agronomists, ecologists, economists, and farmers is required to ensure a holistic view of how perennial low-input bioenergy crops can be integrated and cultivated on (preferably marginal) agricultural land, and how existing agricultural systems can be adapted in a changing world to foster the development of a social-ecologically more sustainable bioeconomy.

Author Contributions

Conceptualization, M.V.C., V.V.C., K.W.-S., B.E., I.L. and B.W.; methodology, M.V.C., V.V.C., K.W.-S., B.E., I.S., M.V.E., S.H. and Y.I.; software, V.V.C., K.W.-S., B.E., I.S., M.V.E.; validation, M.V.C., K.W.-S., B.E., D.S. and I.L.; formal analysis, M.V.C., K.W.-S., B.E., I.L., N.D.J., M.W., J.L., E.M., A.B. and B.W.; investigation, M.V.C., M.W., J.L., E.M., A.B., V.V.C., K.W.-S., B.E., I.S., M.V.E., Y.I., N.D.J., A.L.F., D.S., S.L.C., V.W., I.L. and B.W.; resources, B.E., I.S., M.V.E., K.W.-S., V.W.; data curation, M.V.C., V.V.C., K.W.-S., B.E., I.S. and M.V.E.; writing—original draft preparation, M.V.C., M.W., J.L., E.M., A.B., V.V.C., K.W.-S., B.E., I.S., M.V.E., Y.I., N.D.J., S.H., A.L.F., D.S., S.L.C., V.W., I.L. and B.W.; writing—review and editing, M.V.C.; visualization, M.V.C., V.V.C., K.W.-S., B.E., I.S., M.V.E. and B.W.; supervision, B.E., I.L., N.D.J., A.L.F., S.L.C. and V.W.; project administration, M.V.C., M.W., J.L., E.M., A.B., V.V.C., K.W.-S., B.E., I.S., M.V.E., Y.I., N.D.J., S.H., A.L.F., D.S., S.L.C., V.W., I.L., B.W.; funding acquisition, B.E., A.L.F., D.S., S.L.C., and I.L.

Funding

This research received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 727698 and the University of Hohenheim. N.D.J. received funding from the Bioeconomy Science Center (BioSC), supported in the project AP3 Focus Lab. The scientific activities of the Bioeconomy Science Center were financially supported by the Ministry of Innovation, Science and Research within the framework of the NRW Strategieprojekt BioSC (no. 313/323-400-002 13).

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Scarlat, N. Highlights of the Conference. In Proceedings of the 27th European Biomass Conference & Exhibition, Lisbon, Portugal, 27–30 May 2019; Available online: http://programme.eubce.com/search.php?close=all (accessed on 31 July 2019).
  2. Canadell, J.G.; Schulze, E.D. Global potential of biospheric carbon management for climate mitigation. Nat. Commun. 2014, 5, 5282. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Bui, M.; Adjiman, C.S.; Bardow, A.; Anthony, E.J.; Boston, A.; Brown, S.; Fennell, P.S.; Fuss, S.; Galindo, A.; Hackett, L.A.; et al. Carbon capture and storage (CCS): The way forward. Energy Environ. Sci. 2018, 11, 1062–1176. [Google Scholar] [CrossRef]
  4. Ragauskas, A.J.; Williams, C.K.; Davison, B.H.; Britovsek, G.; Cairney, J.; Eckert, C.A.; Frederick, W.J.; Hallett, J.P.; Leak, D.J.; Liotta, C.L.; et al. The Path Forward for Biofuels and Biomaterials. Science 2006, 311, 484–489. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Karp, A.; Shield, I. Bioenergy from plants and the sustainable yield challenge. New Phytol. 2008, 179, 15–32. [Google Scholar] [CrossRef]
  6. Hastilestari, B.R.; Mudersbach, M.; Tomala, F.; Vogt, H.; Biskupek-Korell, B.; Van Damme, P.; Guretzki, S.; Papenbrock, J. Euphorbia tirucalli L.-Comprehensive Characterization of a Drought Tolerant Plant with a Potential as Biofuel Source. PLoS ONE 2013, 8, e63501. [Google Scholar] [CrossRef]
  7. Hou, Y.-K.; Liu, S.-Y.; Huang, L.; Zhou, H.-J. Selection and evaluation of Bio-diesel tree species in China. For. Res. 2009, 22, 7–13. [Google Scholar]
  8. Kagunyu, A.F.; Wanjohi, J.G. The emergency of Euphorbia tirucalli as drought feeds for camels in northern Kenya. Pastoralism 2015, 5, 17. [Google Scholar] [CrossRef]
  9. Khaleghian, A.; Nakaya, Y.; Nazari, H. Biodiesel production from Euphorbia tirucalli L. J. Med. Plant Res. 2011, 5, 4968–4973. [Google Scholar]
  10. Calabrò, P.S.; Catalán, E.; Folino, A.; Sánchez, A.; Komilis, D. Effect of three pretreatment techniques on the chemical composition and on the methane yields of Opuntia ficus-indica (prickly pear) biomass. Waste Manag. Res. 2018, 36, 17–29. [Google Scholar] [CrossRef]
  11. Santos, T.D.N.; Dutra, E.D.; Gomes do Prado, A.; Leite, F.C.B.; de Souza, R.D.F.R.; dos Santos, D.C.; Moraes de Abreu, C.A.; Simões, D.A.; de Morais, M.A., Jr.; Menezes, R.S.C. Potential for biofuels from the biomass of prickly pear cladodes: Challenges for bioethanol and biogas production in dry areas. Biomass Bioenergy 2016, 85, 215–222. [Google Scholar] [CrossRef]
  12. Yang, L.; Lu, M.; Carl, S.; Mayer, J.A.; Cushman, J.C.; Tian, E.; Lin, H. Biomass characterization of Agave and Opuntia as potential biofuel feedstocks. Biomass Bioenergy 2015, 76, 43–53. [Google Scholar] [CrossRef]
  13. Davis, S.C.; Dohleman, F.G.; Long, S.P. The global potential for Agave as a biofuel feedstock. GCB Bioenergy 2011, 3, 68–78. [Google Scholar] [CrossRef]
  14. Mason, P.M.; Glover, K.; Smith, J.A.C.; Willis, K.J.; Woods, J.; Thompson, I.P. The potential of CAM crops as a globally significant bioenergy resource: Moving from ‘fuel or food’ to ‘fuel and more food’. Energy Environ. Sci. 2015, 8, 2320–2329. [Google Scholar] [CrossRef]
  15. Bartholdsen, H.-K.; Eidens, A.; Löffler, K.; Seehaus, F.; Wejda, F.; Burandt, T.; Oei, P.-Y.; Kemfert, C.; von Hirschhausen, C. Pathways for Germany’s Low-Carbon Energy Transformation Towards 2050. Energies 2019, 12, 2988. [Google Scholar] [CrossRef]
  16. European Commission. A policy framework for climate and energy in the period from 2020 to 2030. Tech. Rep. COM 2014, 15, 2014. [Google Scholar]
  17. Robinius, M.; Otto, A.; Heuser, P.; Welder, L.; Syranidis, K.; Ryberg, D.S.; Grube, T.; Markewitz, P.; Peters, R.; Stolten, D. Linking the power and transport sectors—Part 1: The principle of sector coupling. Energies 2017, 10, 956. [Google Scholar] [CrossRef]
  18. Caspeta, L.; Buijs, N.A.A.; Nielsen, J. The role of biofuels in the future energy supply. Energy Environ. Sci. 2013, 6, 1077–1082. [Google Scholar] [CrossRef] [Green Version]
  19. Kalghatgi, G.; Levinsky, H.; Colket, M. Future transportation fuels. Prog. Energy Combust. Sci. 2018, 69, 103–105. [Google Scholar] [CrossRef]
  20. Inderwildi, O.R.; King, D.A. Quo vadis biofuels? Energy Environ. Sci. 2009, 2, 343–346. [Google Scholar] [CrossRef]
  21. Wang, M.; Dewil, R.; Maniatis, K.; Wheeldon, J.; Tan, T.; Baeyens, J.; Fang, Y. Biomass-derived aviation fuels: Challenges and perspective. Prog. Energy Combust. Sci. 2019, 74, 31–49. [Google Scholar] [CrossRef]
  22. IEA World Energy Outlook 2018—The Gold Standard of Energy Analysis. Available online: https://www.iea.org/weo2018/themes/ (accessed on 8 August 2019).
  23. David, K.; Ragauskas, A.J. Switchgrass as an energy crop for biofuel production: A review of its ligno-cellulosic chemical properties. Energy Environ. Sci. 2010, 3, 1182–1190. [Google Scholar] [CrossRef]
  24. Lask, J.; Wagner, M.; Trindade, L.M.; Lewandowski, I. Life cycle assessment of ethanol production from miscanthus: A comparison of production pathways at two European sites. GCB Bioenergy 2019, 11, 269–288. [Google Scholar] [CrossRef]
  25. Cosentino, S.L.; Copani, V.; Patanè, C.; Mantineo, M.; D’Agosta, G.M. Agronomic, energetic and environmental aspects of biomass energy crops suitable for Italian environments. Ital. J. Agron. 2008, 3, 81–95. [Google Scholar] [CrossRef]
  26. Weiland, P. Biogas production: Current state and perspectives. Appl. Microbiol. Biotechnol. 2010, 85, 849–860. [Google Scholar] [CrossRef] [PubMed]
  27. Weiland, P. Production and energetic use of biogas from energy crops and wastes in Germany. Appl. Biochem. Biotechnol. 2003, 109, 263–274. [Google Scholar] [CrossRef]
  28. Scarlat, N.; Dallemand, J.-F.; Fahl, F. Biogas: Developments and perspectives in Europe. Renew. Energy 2018, 129, 457–472. [Google Scholar] [CrossRef]
  29. Pandiyan, K.; Singh, A.; Singh, S.; Saxena, A.K.; Nain, L. Technological interventions for utilization of crop residues and weedy biomass for second generation bio-ethanol production. Renew. Energy 2019, 132, 723–741. [Google Scholar] [CrossRef]
  30. Oleskowicz-Popiel, P.; Kádár, Z.; Heiske, S.; Klein-Marcuschamer, D.; Simmons, B.A.; Blanch, H.W.; Schmidt, J.E. Co-production of ethanol, biogas, protein fodder and natural fertilizer in organic farming–evaluation of a concept for a farm-scale biorefinery. Bioresour. Technol. 2012, 104, 440–446. [Google Scholar] [CrossRef]
  31. Taube, F.; Herrmann, A. Kriterien für einen nachhaltigen Maisanbau zur Biogaserzeugung. Christian-Albrechts-Universität zu Kiel. 2007. Available online: http://www.grassland-organicfarming.uni-kiel.de/gfo/pdf/DMK_Taube07.pdf (accessed on 1 October 2019).
  32. Serdjuk, M.; Bodmer, U.; Hülsbergen, K.-J. Integration of biogas production into organic arable farming systems: Crop yield response and economic effects. Org. Agric. 2018, 8, 301–314. [Google Scholar] [CrossRef]
  33. Keegan, D.; Kretschmer, B.; Elbersen, B.; Panoutsou, C. Cascading use: A systematic approach to biomass beyond the energy sector. Biofuels Bioprod. Biorefining 2013, 7, 193–206. [Google Scholar] [CrossRef]
  34. Philippidis, G.; Bartelings, H.; Helming, J.; M’barek, R.; Smeets, E.; Van Meijl, H. The Good, the Bad and the Uncertain: Bioenergy Use in the European Union. Energies 2018, 11, 2703. [Google Scholar] [CrossRef]
  35. Zörb, C.; Lewandowski, I.; Kindervater, R.; Göttert, U.; Patzelt, D. Biobased Resources and Value Chains. In Bioeconomy; Lewandowski, I., Ed.; Springer: Cham, Switzerland, 2018; pp. 75–97. [Google Scholar]
  36. Pires, J.R.A.; Souza, V.G.L.; Fernando, A.L. Valorization of energy crops as a source for nanocellulose production—Current knowledge and future prospects. Ind. Crops Prod. 2019, 140, 111642. [Google Scholar] [CrossRef]
  37. Tilman, D.; Socolow, R.; Foley, J.A.; Hill, J.; Larson, E.; Lynd, L.; Pacala, S.; Reilly, J.; Searchinger, T.; Somerville, C. Beneficial biofuels—the food, energy, and environment trilemma. Science 2009, 325, 270–271. [Google Scholar] [CrossRef] [PubMed]
  38. Araújo, K.; Mahajan, D.; Kerr, R.; Silva, M.D. Global biofuels at the crossroads: An overview of technical, policy, and investment complexities in the sustainability of biofuel development. Agriculture 2017, 7, 32. [Google Scholar] [CrossRef]
  39. Sheppard, A.W.; Gillespie, I.; Hirsch, M.; Begley, C. Biosecurity and sustainability within the growing global bioeconomy. Curr. Opin. Environ. Sustain. 2011, 3, 4–10. [Google Scholar] [CrossRef]
  40. Elshout, P.M.F.; van Zelm, R.; van der Velde, M.; Steinmann, Z.; Huijbregts, M.A.J. Global relative species loss due to first-generation biofuel production for the transport sector. GCB Bioenergy 2019, 11, 763–772. [Google Scholar] [CrossRef] [PubMed]
  41. Mishra, S.K.; Negri, M.C.; Kozak, J.; Cacho, J.F.; Quinn, J.; Secchi, S.; Ssegane, H. Valuation of ecosystem services in alternative bioenergy landscape scenarios. GCB Bioenergy 2019, 11, 748–762. [Google Scholar] [CrossRef] [Green Version]
  42. Allen, B.R.; Keegan, D.; Elbersen, B. Biomass and bioenergy in the wider land-use context of the European Union. Biofuels Bioprod. Biorefining 2013, 7, 207–216. [Google Scholar] [CrossRef]
  43. Valentine, J.; Clifton-Brown, J.; Hastings, A.; Robson, P.; Allison, G.; Smith, P. Food vs. fuel: The use of land for lignocellulosic “next generation” energy crops that minimize competition with primary food production. GCB Bioenergy 2012, 4, 1–19. [Google Scholar] [CrossRef]
  44. Doelman, J.C.; Stehfest, E.; Tabeau, A.; van Meijl, H. Making the Paris agreement climate targets consistent with food security objectives. Glob. Food Secur. 2019, 23, 93–103. [Google Scholar] [CrossRef]
  45. Michel, H. Editorial: The Nonsense of Biofuels. Angew. Chem. Int. Ed. 2012, 51, 2516–2518. [Google Scholar] [CrossRef] [PubMed]
  46. Von Cossel, M.; Elbersen, B.; Von Cossel, V.; Staritsky, I.; Van Eupen, M.; Mantel, S.; Iqbal, I.; Happe, S.; Scordia, D.; Cosentino, S.L.; et al. How to feed the European bioeconomy in the future? Climate change-forced shifts in growth suitability of industrial crops until 2100. manuscript in preparation.
  47. Winkler, B.; Mangold, A.; Von Cossel, M.; Iqbal, Y.; Kiesel, A.; Lewandowski, I. Implementing miscanthus into sustainable farming systems: A review on agronomic practices, capital and labor demand. Renew. Sustain. Energy Rev. under review.
  48. Elbersen, B.; Van Eupen, M.; Verzandvoort, S.; Boogaard, H.; Mucher, S.; Cicarreli, T.; Elbersen, W.; Mantel, S.; Bai, Z.; MCallum, I.; et al. Methodological Approaches to Identify and Map Marginal Land Suitable for Industrial Crops in Europe; WUR: Wageningen, The Netherlands, 2018; p. 142. [Google Scholar]
  49. Fajardy, M.; Chiquier, S.; Mac Dowell, N. Investigating the BECCS resource nexus: Delivering sustainable negative emissions. Energy Environ. Sci. 2018, 11, 3408–3430. [Google Scholar] [CrossRef]
  50. Elbersen, B.; Fritsche, U.; Petersen, J.-E.; Lesschen, J.P.; Böttcher, H.; Overmars, K. Assessing the effect of stricter sustainability criteria on EU biomass crop potential. Biofuels Bioprod. Biorefining 2013, 7, 173–192. [Google Scholar] [CrossRef]
  51. Von Cossel, M.; Lewandowski, I.; Elbersen, B.; Staritsky, I.; Van Eupen, M.; Iqbal, Y.; Mantel, S.; Scordia, D.; Testa, G.; Cosentino, S.L.; et al. Marginal agricultural land low-input systems for biomass production. Energies 2019, 12, 3123. [Google Scholar] [CrossRef]
  52. Wagner, M.; Mangold, A.; Lask, J.; Petig, E.; Kiesel, A.; Lewandowski, I. Economic and environmental performance of miscanthus cultivated on marginal land for biogas production. GCB Bioenergy 2019, 11, 34–49. [Google Scholar] [CrossRef]
  53. Zegada-Lizarazu, W.; Elbersen, H.W.; Cosentino, S.L.; Zatta, A.; Alexopoulou, E.; Monti, A. Agronomic aspects of future energy crops in Europe. Biofuels Bioprod. Biorefining 2010, 4, 674–691. [Google Scholar] [CrossRef]
  54. Smeets, E.M.W.; Faaij, A.P.C.; Lewandowski, I.M.; Turkenburg, W.C. A bottom-up assessment and review of global bio-energy potentials to 2050. Prog. Energy Combust. Sci. 2007, 33, 56–106. [Google Scholar] [CrossRef] [Green Version]
  55. Elbersen, B.; Van Verzandvoort, M.; Boogaard, S.; Mucher, S.; Cicarelli, T.; Elbersen, W.; Mantel, S.; Bai, Z.; MCallum, I.; Iqbal, Y.; et al. Definition and Classification of Marginal Lands Suitable for Industrial Crops in Europe (EU Deliverable); WUR: Wageningen, The Netherlands, 2018; p. 44. [Google Scholar]
  56. Ceotto, E.; Di Candilo, M. Sustainable bioenergy production, land and nitrogen use. In Biodiversity, Biofuels, Agroforestry and Conservation Agriculture; Lichtfouse, E., Ed.; Springer: Dordrecht, The Netherlands; Berlin/Heidelberg, Germany, 2010; pp. 101–122. [Google Scholar]
  57. Cai, X.; Zhang, X.; Wang, D. Land availability for biofuel production. Environ. Sci. Technol. 2011, 45, 334–339. [Google Scholar] [CrossRef]
  58. Von Cossel, M.; Bauerle, A.; Boob, M.; Thumm, U.; Elsaesser, M.; Lewandowski, I. The Performance of Mesotrophic Arrhenatheretum Grassland under Different Cutting Frequency Regimes for Biomass Production in Southwest Germany. Agriculture 2019, 9, 199. [Google Scholar] [CrossRef]
  59. Boob, M.; Truckses, B.; Seither, M.; Elsäßer, M.; Thumm, U.; Lewandowski, I. Management effects on botanical composition of species-rich meadows within the Natura 2000 network. Biodivers. Conserv. 2019, 28, 729–750. [Google Scholar] [CrossRef]
  60. Scordia, D.; Cosentino, S.L. Perennial Energy Grasses: Resilient Crops in a Changing European Agriculture. Agriculture 2019, 9, 169. [Google Scholar] [CrossRef]
  61. Gützloe, A.; Thumm, U.; Lewandowski, I. Influence of climate parameters and management of permanent grassland on biogas yield and GHG emission substitution potential. Biomass Bioenergy 2014, 64, 175–189. [Google Scholar] [CrossRef]
  62. Fajardy, M.; Mac Dowell, N. The energy return on investment of BECCS: Is BECCS a threat to energy security? Energy Environ. Sci. 2018, 11, 1581–1594. [Google Scholar] [CrossRef]
  63. Nakajima, T.; Yamada, T.; Anzoua, K.G.; Kokubo, R.; Noborio, K. Carbon sequestration and yield performances of Miscanthus × giganteus and Miscanthus sinensis. Carbon Manag. 2018, 9, 415–423. [Google Scholar] [CrossRef]
  64. Searchinger, T.D.; Beringer, T.; Holtsmark, B.; Kammen, D.M.; Lambin, E.F.; Lucht, W.; Raven, P.; van Ypersele, J.-P. Europe’s renewable energy directive poised to harm global forests. Nat. Commun. 2018, 9, 3741. [Google Scholar] [CrossRef] [PubMed]
  65. Verdade, L.M.; Piña, C.I.; Rosalino, L.M. Biofuels and biodiversity: Challenges and opportunities. Environ. Dev. 2015, 15, 64–78. [Google Scholar] [CrossRef]
  66. Winkler, B.; Lemke, S.; Ritter, J.; Lewandowski, I. Integrated assessment of renewable energy potential: Approach and application in rural South Africa. Environ. Innov. Soc. Transit. 2017, 24, 17–31. [Google Scholar] [CrossRef]
  67. Michalscheck, M. On Smallholder Farm and Farmer Diversity. Dissertation, Wageningen University & Research, Wageningen, The Netherlands, 2019. [Google Scholar]
  68. He, G.; Zhao, Y.; Wang, L.; Jiang, S.; Zhu, Y. China’s food security challenge: Effects of food habit changes on requirements for arable land and water. J. Clean. Prod. 2019, 229, 739–750. [Google Scholar] [CrossRef]
  69. Fischer, J.; Brosi, B.; Daily, G.C.; Ehrlich, P.R.; Goldman, R.; Goldstein, J.; Lindenmayer, D.B.; Manning, A.D.; Mooney, H.A.; Pejchar, L.; et al. Should agricultural policies encourage land sparing or wildlife-friendly farming? Front. Ecol. Environ. 2008, 6, 380–385. [Google Scholar] [CrossRef]
  70. Tscharntke, T.; Clough, Y.; Wanger, T.C.; Jackson, L.; Motzke, I.; Perfecto, I.; Vandermeer, J.; Whitbread, A. Global food security, biodiversity conservation and the future of agricultural intensification. Biol. Conserv. 2012, 151, 53–59. [Google Scholar] [CrossRef]
  71. Danish, K.; Wang, Z. Does biomass energy consumption help to control environmental pollution? Evidence from BRICS countries. Sci. Total Environ. 2019, 670, 1075–1083. [Google Scholar] [CrossRef] [PubMed]
  72. Green, R.E.; Cornell, S.J.; Scharlemann, J.P.; Balmford, A. Farming and the fate of wild nature. Science 2005, 307, 550–555. [Google Scholar] [CrossRef] [PubMed]
  73. Griggs, D.; Stafford-Smith, M.; Gaffney, O.; Rockström, J.; Öhman, M.C.; Shyamsundar, P.; Steffen, W.; Glaser, G.; Kanie, N.; Noble, I. Policy: Sustainable development goals for people and planet. Nature 2013, 495, 305. [Google Scholar] [CrossRef]
  74. Robert, K.W.; Parris, T.M.; Leiserowitz, A.A. What is sustainable development? Goals, indicators, values, and practice. Environ. Sci. Policy Sustain. Dev. 2005, 47, 8–21. [Google Scholar] [CrossRef]
  75. Altieri, M.A. Agroecology: The Science of Sustainable Agriculture; CRC Press: Boca Raton, FL, USA, 2018. [Google Scholar]
  76. Altieri, M.A.; Nicholls, C.I.; Montalba, R. Technological Approaches to Sustainable Agriculture at a Crossroads: An Agroecological Perspective. Sustainability 2017, 9, 349. [Google Scholar] [CrossRef]
  77. Uphoff, N.T.; Altieri, M.A. Alternatives to Conventional Modern Agriculture for Meeting World Needs in the Next Century: Report of a Conference on Sustainable Agriculture, Evaluation of New Paradigms and Old Practices; Cornell International Institute for Food, Agriculture and Development: Bellagio, Italy, 1999. [Google Scholar]
  78. Elbersen, B.; Van Eupen, M.; Alexopoulou, E.; Bai, Z.; Boogaard, H.; Carrasco, J.E.; Ceccarelli, T.; Ciria Ramos, C.; Ciria, P.; Cosentino, S.L.; et al. Mapping Marginal Land Potentially Available for Industrial Crops in Europe; Visual presentation at the 26th European Biomass Conference & Exhibition, Copenhagen, Denmark, 2018. Available online: https://www.researchgate.net/publication/325272893_Mapping_Marginal_land_potentially_available_for_industrial_crops_in_Europe (accessed on 1 October 2019).
  79. Ramirez-Almeyda, J.; Elbersen, B.; Monti, A.; Staritsky, I.; Panoutsou, C.; Alexopoulou, E.; Schrijver, R.; Elbersen, W. Assessing the Potentials for Nonfood Crops. In Modeling and Optimization of Biomass Supply Chains; Panoutsou, C., Ed.; Elsevier: Amsterdam, The Netherlands, 2017; pp. 219–251. [Google Scholar]
  80. Pachauri, R.K.; Allen, M.R.; Barros, V.R.; Broome, J.; Cramer, W.; Christ, R.; Church, J.A.; Clarke, L.; Dahe, Q.; Dasgupta, P. Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change; IPCC: Geneva, Switzerland, 2014. [Google Scholar]
  81. Krasuska, E.; Cadórniga, C.; Tenorio, J.L.; Testa, G.; Scordia, D. Potential land availability for energy crops production in Europe. Biofuels Bioprod. Biorefining 2010, 4, 658–673. [Google Scholar] [CrossRef]
  82. Ciria, C.S.; Sanz, M.; Carrasco, J.; Ciria, P. Identification of Arable Marginal Lands under Rainfed Conditions for Bioenergy Purposes in Spain. Sustainability 2019, 11, 1833. [Google Scholar] [CrossRef]
  83. Xue, S.; Lewandowski, I.; Wang, X.; Yi, Z. Assessment of the production potentials of Miscanthus on marginal land in China. Renew. Sustain. Energy Rev. 2016, 54, 932–943. [Google Scholar] [CrossRef]
  84. McIntyre, B.D. International Assessment of Agricultural Knowledge, Science and Technology for Development (IAASTD): Synthesis Report with Executive Summary: A Synthesis of the Global and Sub-Global IAASTD Reports; IAASTD, Island Press: Washington, DC, USA, 2009. [Google Scholar]
  85. TEEB. Guidance Manual for TEEB Country Studies-Version 1.0; Institute for European Environmental Policy: London, UK, 2013. [Google Scholar]
  86. Nabel, M.; Schrey, S.D.; Temperton, V.M.; Harrison, L.; Jablonowski, N.D. Legume Intercropping With the Bioenergy Crop Sida hermaphrodita on Marginal Soil. Front. Plant Sci. 2018, 9, 905. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  87. Nabel, M.; Barbosa, D.B.P.; Horsch, D.; Jablonowski, N.D. Energy Crop (Sida Hermaphrodita) Fertilization Using Digestate under Marginal Soil Conditions: A Dose-response Experiment. Energy Procedia 2014, 59, 127–133. [Google Scholar] [CrossRef] [Green Version]
  88. Von Cossel, M.; Lewandowski, I. Perennial wild plant mixtures for biomass production: Impact of species composition dynamics on yield performance over a five-year cultivation period in southwest Germany. Eur. J. Agron. 2016, 79, 74–89. [Google Scholar] [CrossRef]
  89. Emmerling, C. Impact of land-use change towards perennial energy crops on earthworm population. Appl. Soil Ecol. 2014, 84, 12–15. [Google Scholar] [CrossRef]
  90. Von Cossel, M.; Winkler, B.; Mangold, A.; Lewandowski, I.; Elbersen, B.; Wagner, M.; Magenau, E.; Lask, I.; Staritsky, I.; Van Eupen, M.; et al. Bridging the gap between biofuels and biodiversity for a bioeconomy transition – Social-ecological implications of miscanthus cultivation for isobutanol production. Energy Environ. Sci. under review.
  91. Kiesel, A.; Wagner, M.; Lewandowski, I. Environmental performance of miscanthus, switchgrass and maize: Can C4 perennials increase the sustainability of biogas production? Sustainability 2017, 9, 5. [Google Scholar] [CrossRef]
  92. Kalt, G.; Mayer, A.; Theurl, M.C.; Lauk, C.; Erb, K.-H.; Haberl, H. Natural climate solutions versus bioenergy: Can carbon benefits of natural succession compete with bioenergy from short rotation coppice? GCB Bioenergy 2019, in press. Available online: https://onlinelibrary.wiley.com/doi/full/10.1111/gcbb.12626 (accessed on 1 October 2019). [CrossRef]
  93. Secretariat of the Convention on Biological Diversity. Global Biodiversity Outlook 3; Secretariat of the Convention on Biological Diversity: Montreal, QC, Canada, 2010. [Google Scholar]
  94. Grooten, M.; Almond, R.E.A. Living Planet Report 2018. Aiming Higher; WWF: Gland, Switzerland, 2018. [Google Scholar]
  95. Dauber, J.; Bolte, A. Bioenergy: Challenge or support for the conservation of biodiversity? GCB Bioenergy 2014, 6, 180–182. [Google Scholar] [CrossRef] [Green Version]
  96. Immerzeel, D.J.; Verweij, P.A.; van der Hilst, F.; Faaij, A.P. Biodiversity impacts of bioenergy crop production: A state-of-the-art review. GCB Bioenergy 2014, 6, 183–209. [Google Scholar] [CrossRef]
  97. Pedroli, B.; Elbersen, B.; Frederiksen, P.; Grandin, U.; Heikkilä, R.; Krogh, P.H.; Izakovičová, Z.; Johansen, A.; Meiresonne, L.; Spijker, J. Is energy cropping in Europe compatible with biodiversity?—Opportunities and threats to biodiversity from land-based production of biomass for bioenergy purposes. Biomass Bioenergy 2013, 55, 73–86. [Google Scholar] [CrossRef]
  98. Chmelíková, L.; Wolfrum, S. Mitigating the biodiversity footprint of energy crops–A case study on arthropod diversity. Biomass Bioenergy 2019, 125, 180–187. [Google Scholar] [CrossRef]
  99. Semere, T.; Slater, F.M. Invertebrate populations in miscanthus (Miscanthus × giganteus) and reed canary-grass (Phalaris arundinacea) fields. Biomass Bioenergy 2007, 31, 30–39. [Google Scholar] [CrossRef]
  100. Semere, T.; Slater, F.M. Ground flora, small mammal and bird species diversity in miscanthus (Miscanthus × giganteus) and reed canary-grass (Phalaris arundinacea) fields. Biomass Bioenergy 2007, 31, 20–29. [Google Scholar] [CrossRef]
  101. Haughton, A.J.; Bond, A.J.; Lovett, A.A.; Dockerty, T.; Sünnenberg, G.; Clark, S.J.; Bohan, D.A.; Sage, R.B.; Mallott, M.D.; Mallott, V.E.; et al. A novel, integrated approach to assessing social, economic and environmental implications of changing rural land-use: A case study of perennial biomass crops. J. Appl. Ecol. 2009, 46, 315–322. [Google Scholar] [CrossRef]
  102. Haughton, A.J.; Bohan, D.A.; Clark, S.J.; Mallott, M.D.; Mallott, V.; Sage, R.; Karp, A. Dedicated biomass crops can enhance biodiversity in the arable landscape. GCB Bioenergy 2016, 8, 1071–1081. [Google Scholar] [CrossRef] [PubMed]
  103. Felton, A.; Knight, E.; Wood, J.; Zammit, C.; Lindenmayer, D. A meta-analysis of fauna and flora species richness and abundance in plantations and pasture lands. Biol. Conserv. 2010, 143, 545–554. [Google Scholar] [CrossRef] [Green Version]
  104. Van der Hilst, F.; Lesschen, J.P.; Van Dam, J.M.C.; Riksen, M.; Verweij, P.A.; Sanders, J.P.M.; Faaij, A.P.C. Spatial variation of environmental impacts of regional biomass chains. Renew. Sustain. Energy Rev. 2012, 16, 2053–2069. [Google Scholar] [CrossRef]
  105. Werling, B.P.; Dickson, T.L.; Isaacs, R.; Gaines, H.; Gratton, C.; Gross, K.L.; Liere, H.; Malmstrom, C.M.; Meehan, T.D.; Ruan, L. Perennial grasslands enhance biodiversity and multiple ecosystem services in bioenergy landscapes. Proc. Natl. Acad. Sci. USA 2014, 111, 1652–1657. [Google Scholar] [CrossRef] [Green Version]
  106. Pulighe, G.; Bonati, G.; Colangeli, M.; Morese, M.M.; Traverso, L.; Lupia, F.; Khawaja, C.; Janssen, R.; Fava, F. Ongoing and emerging issues for sustainable bioenergy production on marginal lands in the Mediterranean regions. Renew. Sustain. Energy Rev. 2019, 103, 58–70. [Google Scholar] [CrossRef]
  107. Williams, M.A.; Feest, A. The Effect of Miscanthus Cultivation on the Biodiversity of Ground Beetles (Coleoptera: Carabidae), Spiders and Harvestmen (Arachnida: Araneae and Opiliones). Agric. Sci. 2019, 10, 903–917. [Google Scholar] [CrossRef] [Green Version]
  108. Von Cossel, M. Agricultural Diversification of Biogas Crop Cultivation. Dissertation, University of Hohenheim, Stuttgart, Germany, 2019. [Google Scholar]
  109. Weisser, W.W.; Roscher, C.; Meyer, S.T.; Ebeling, A.; Luo, G.; Allan, E.; Beßler, H.; Barnard, R.L.; Buchmann, N.; Buscot, F. Biodiversity effects on ecosystem functioning in a 15-year grassland experiment: Patterns, mechanisms, and open questions. Basic Appl. Ecol. 2017, 23, 1–73. [Google Scholar] [CrossRef]
  110. Whitaker, J.; Field, J.L.; Bernacchi, C.J.; Cerri, C.E.; Ceulemans, R.; Davies, C.A.; DeLucia, E.H.; Donnison, I.S.; McCalmont, J.P.; Paustian, K. Consensus, uncertainties and challenges for perennial bioenergy crops and land use. GCB Bioenergy 2018, 10, 150–164. [Google Scholar] [CrossRef] [PubMed]
  111. Dauber, J.; Brown, C.; Fernando, A.L.; Finnan, J.; Krasuska, E.; Ponitka, J.; Styles, D.; Thrän, D.; Van Groenigen, K.J.; Weih, M. Bioenergy from “surplus” land: Environmental and socio-economic implications. BioRisk Biodivers. Ecosyst. Risk Assess. 2012, 7, 5–50. [Google Scholar] [CrossRef]
  112. Wiens, J.; Fargione, J.; Hill, J. Biofuels and biodiversity. Ecol. Appl. 2011, 21, 1085–1095. [Google Scholar] [CrossRef] [PubMed]
  113. Manning, P.; Taylor, G.; Hanley, E.M. Bioenergy, food production and biodiversity—An unlikely alliance? GCB Bioenergy 2015, 7, 570–576. [Google Scholar] [CrossRef]
  114. Groom, M.J.; Gray, E.M.; Townsend, P.A. Biofuels and biodiversity: Principles for creating better policies for biofuel production. Conserv. Biol. 2008, 22, 602–609. [Google Scholar] [CrossRef] [PubMed]
  115. Von Cossel, M.; Mangold, A.; Iqbal, Y.; Hartung, J.; Lewandowski, I.; Kiesel, A. How to Generate Yield in the First Year—A Three-Year Experiment on Miscanthus (Miscanthus × giganteus (Greef et Deuter)) Establishment under Maize (Zea mays L.). Agronomy 2019, 9, 237. [Google Scholar] [CrossRef]
  116. Himanen, S.; Mäkinen, H.; Rimhanen, K.; Savikko, R. Engaging farmers in climate change adaptation planning: Assessing intercropping as a means to support farm adaptive capacity. Agriculture 2016, 6, 34. [Google Scholar] [CrossRef]
  117. Gruenewald, H.; Brandt, B.K.V.; Schneider, B.U.; Bens, O.; Kendzia, G.; Hüttl, R.F. Agroforestry systems for the production of woody biomass for energy transformation purposes. Ecol. Eng. 2007, 29, 319–328. [Google Scholar] [CrossRef]
  118. Volk, T.A.; Abrahamson, L.P.; Nowak, C.A.; Smart, L.B.; Tharakan, P.J.; White, E.H. The development of short-rotation willow in the northeastern United States for bioenergy and bioproducts, agroforestry and phytoremediation. Biomass Bioenergy 2006, 30, 715–727. [Google Scholar] [CrossRef]
  119. Jensen, E.S.; Peoples, M.B.; Boddey, R.M.; Gresshoff, P.M.; Henrik, H.-N.; Alves, B.J.R.; Morrison, M.J. Legumes for mitigation of climate change and the provision of feedstock for biofuels and biorefineries. A review. Agron. Sustain. Dev. 2012, 32, 329–364. [Google Scholar] [CrossRef]
  120. Timsina, J. Can organic sources of nutrients increase crop yields to meet global food demand? Agronomy 2018, 8, 214. [Google Scholar] [CrossRef]
  121. Weißhuhn, P.; Reckling, M.; Stachow, U.; Wiggering, H. Supporting Agricultural Ecosystem Services through the Integration of Perennial Polycultures into Crop Rotations. Sustainability 2017, 9, 2267. [Google Scholar] [CrossRef]
  122. Von Cossel, M.; Steberl, K.; Hartung, J.; Agra Pereira, L.; Kiesel, A.; Lewandowski, I. Methane yield and species diversity dynamics of perennial wild plant mixtures established alone, under cover crop maize (Zea mays L.) and after spring barley (Hordeum vulgare L.). GCB Bioenergy. 2019. in press. Available online: https://onlinelibrary.wiley.com/doi/full/10.1111/gcbb.12640 (accessed on 1 October 2019). [CrossRef]
  123. Bybee-Finley, K.A.; Ryan, M.R. Advancing Intercropping Research and Practices in Industrialized Agricultural Landscapes. Agriculture 2018, 8, 80. [Google Scholar] [CrossRef]
  124. Pagano, M.C.; Correa, E.J.A.; Duarte, N.F.; Yelikbayev, B.; O’Donovan, A.; Gupta, V.K. Advances in Eco-Efficient Agriculture: The Plant-Soil Mycobiome. Agriculture 2017, 7, 14. [Google Scholar] [CrossRef]
  125. Wienforth, B.; Knieb, A.; Böttcher, U.; Herrmann, A.; Sieling, K.; Taube, F.; Kage, H. Evaluating Bioenergy Cropping Systems towards Productivity and Resource Use Efficiencies: An Analysis Based on Field Experiments and Simulation Modelling. Agronomy 2018, 8, 117. [Google Scholar] [CrossRef]
  126. Mockshell, J.; Kamanda, J. Beyond the Agroecological and Sustainable Agricultural Intensification Debate: Is Blended Sustainability the Way Forward? Int. J. Agric. Sustain. 2018, 16, 127–149. [Google Scholar] [CrossRef]
  127. Zegada-Lizarazu, W.; Monti, A. Energy crops in rotation. A review. Biomass Bioenergy 2011, 35, 12–25. [Google Scholar] [CrossRef]
  128. Herrmann, C.; Idler, C.; Heiermann, M. Biogas crops grown in energy crop rotations: Linking chemical composition and methane production characteristics. Bioresour. Technol. 2016, 206, 23–35. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  129. Von Cossel, M.; Möhring, J.; Kiesel, A.; Lewandowski, I. Methane yield performance of amaranth (Amaranthus hypochondriacus L.) and its suitability for legume intercropping in comparison to maize (Zea mays L.). Ind. Crops Prod. 2017, 103, 107–121. [Google Scholar] [CrossRef]
  130. Nurk, L.; Graß, R.; Pekrun, C.; Wachendorf, M. Effect of sowing method and weed control on the performance of maize (Zea mays L.) intercropped with climbing beans (Phaseolus vulgaris L.). Agriculture 2017, 7, 51. [Google Scholar] [CrossRef]
  131. Von Cossel, M.; Iqbal, Y.; Lewandowski, I. Improving the Ecological Performance of Miscanthus (Miscanthus × giganteus Greef et Deuter) through Intercropping with Woad (Isatis tinctoria L.) and Yellow Melilot (Melilotus officinalis L.). Agriculture 2019, 9, 194. [Google Scholar] [CrossRef]
  132. Nabel, M.; Temperton, V.M.; Poorter, H.; Lücke, A.; Jablonowski, N.D. Energizing marginal soils—The establishment of the energy crop Sida hermaphrodita as dependent on digestate fertilization, NPK, and legume intercropping. Biomass Bioenergy 2016, 87, 9–16. [Google Scholar] [CrossRef]
  133. Berti, M.; Samarappuli, D.; Johnson, B.L.; Gesch, R.W. Integrating winter camelina into maize and soybean cropping systems. Ind. Crops Prod. 2017, 107, 595–601. [Google Scholar] [CrossRef]
  134. Zanetti, F.; Monti, A.; Berti, M.T. Challenges and opportunities for new industrial oilseed crops in EU-27: A review. Ind. Crops Prod. 2013, 50, 580–595. [Google Scholar] [CrossRef]
  135. Royo-Esnal, A.; Valencia-Gredilla, F. Camelina as a rotation crop for weed control in organic farming in a semiarid mediterranean climate. Agriculture 2018, 8, 156. [Google Scholar] [CrossRef]
  136. Stolzenburg, K.; Bruns, H.; Monkos, A.; Ott, J.; Schickler, J. Produktion von Kosubstraten für die Biogasanlage—Ergebnisse der Versuche mit Durchwachsener Silphie (Silphium perfoliatum L.) in Baden-Württemberg. Landwirtschaftliches Technologiezentrum Augustenberg: Karlsruhe, Germany, 2016. [Google Scholar]
  137. Nicholls, C.I.; Altieri, M.A. Plant biodiversity enhances bees and other insect pollinators in agroecosystems. A review. Agron. Sustain. Dev. 2013, 33, 257–274. [Google Scholar] [CrossRef]
  138. Hallmann, C.A.; Sorg, M.; Jongejans, E.; Siepel, H.; Hofland, N.; Schwan, H.; Stenmans, W.; Müller, A.; Sumser, H.; Hörren, T. More than 75 percent decline over 27 years in total flying insect biomass in protected areas. PLoS ONE 2017, 12, e0185809. [Google Scholar] [CrossRef]
  139. Isbell, F.; Adler, P.R.; Eisenhauer, N.; Fornara, D.; Kimmel, K.; Kremen, C.; Letourneau, D.K.; Liebman, M.; Polley, H.W.; Quijas, S. Benefits of increasing plant diversity in sustainable agroecosystems. J. Ecol. 2017, 105, 871–879. [Google Scholar] [CrossRef] [Green Version]
  140. Kuhn, W.; Zeller, J.; Bretschneider-Herrmann, N.; Drenckhahn, K. Energy from Wild Plants—Practical Tips for the Cultivation of Wild Plants to Create Biomass for Biogas Generation Plants, Netzwerk Lebensraum Feldflur c/o Deutsche Wildtier Stiftung, Hamburg, Germany. 2014. Available online: http://cic-wildlife.org/wp-content/uploads/2014/09/English_Praxisratgeber2014.pdf (accessed on 1 October 2019).
  141. Frick, M.; Pfender, G. AG Wildpflanzen-Biogas Kißlegg. In Biogas aus Wildpflanzen – Chancen und Herausforderungen mehrjähriger Wildpflanzenmischungen zur Biogasnutzung aus Sicht der Forschung und Praxis; University of Hohenheim: Stuttgart, Germany, 2019. [Google Scholar]
  142. Zanetti, F.; Eynck, C.; Christou, M.; Krzyżaniak, M.; Righini, D.; Alexopoulou, E.; Stolarski, M.J.; Van Loo, E.N.; Puttick, D.; Monti, A. Agronomic performance and seed quality attributes of Camelina (Camelina sativa L. crantz) in multi-environment trials across Europe and Canada. Ind. Crops Prod. 2017, 107, 602–608. [Google Scholar] [CrossRef] [Green Version]
  143. Stolarski, M.J.; Krzyżaniak, M.; Tworkowski, J.; Załuski, D.; Kwiatkowski, J.; Szczukowski, S. Camelina and crambe production—Energy efficiency indices depending on nitrogen fertilizer application. Ind. Crops Prod. 2019, 137, 386–395. [Google Scholar] [CrossRef]
  144. Alexopoulou, E.; Li, D.; Papatheohari, Y.; Siqi, H.; Scordia, D.; Testa, G. How kenaf (Hibiscus cannabinus L.) can achieve high yields in Europe and China. Ind. Crops Prod. 2015, 68, 131–140. [Google Scholar] [CrossRef]
  145. Väisänen, T.; Batello, P.; Lappalainen, R.; Tomppo, L. Modification of hemp fibers (Cannabis Sativa L.) for composite applications. Ind. Crops Prod. 2018, 111, 422–429. [Google Scholar] [CrossRef]
  146. Manninen, P.; Mäkelä, P.; Hartikainen, H.; Santanen, A.; Seppänen, M.; Stoddard, F.; Yli-Halla, M. Growth of hemp and Lupin in chromium, Arsenic and copper contaminated soil. Ital. J. Agron. 2008, 3, 57–58. [Google Scholar]
  147. Scheliga, M.; Brand, U.; Türk, O.; Gruber, S.; Medina, L.; Petersen, J. Yield and quality of bast fibre from Abutilon theophrasti (Medic.) in southwest Germany depending on the site and fibre extraction method. Ind. Crops Prod. 2018, 121, 320–327. [Google Scholar] [CrossRef]
  148. da Silva, M.J.; Carneiro, P.C.S.; de Souza Carneiro, J.E.; Damasceno, C.M.B.; Parrella, N.N.L.D.; Pastina, M.M.; Simeone, M.L.F.; Schaffert, R.E.; da Costa Parrella, R.A. Evaluation of the potential of lines and hybrids of biomass sorghum. Ind. Crops Prod. 2018, 125, 379–385. [Google Scholar] [CrossRef]
  149. Stolarski, M.J.; Niksa, D.; Krzyżaniak, M.; Tworkowski, J.; Szczukowski, S. Willow productivity from small-and large-scale experimental plantations in Poland from 2000 to 2017. Renew. Sustain. Energy Rev. 2019, 101, 461–475. [Google Scholar] [CrossRef]
  150. Iqbal, Y.; Steberl, K.; Hartung, K.; Lewandowski, I. Optimal sampling area determination for willow by evaluating variability in yield and quality. Ind. Crops Prod. 2019, 134, 265–270. [Google Scholar] [CrossRef]
  151. Gansberger, M.; Montgomery, L.F.R.; Liebhard, P. Botanical characteristics, crop management and potential of Silphium perfoliatum L. as a renewable resource for biogas production: A review. Ind. Crops Prod. 2015, 63, 362–372. [Google Scholar] [CrossRef]
  152. Mast, B.; Lemmer, A.; Oechsner, H.; Reinhardt-Hanisch, A.; Claupein, W.; Graeff-Hönninger, S. Methane yield potential of novel perennial biogas crops influenced by harvest date. Ind. Crops Prod. 2014, 58, 194–203. [Google Scholar] [CrossRef]
  153. Eberl, V.; Fahlbusch, W.; Fritz, M.; Sauer, B. Screening und Selektion von Amarantsorten und -linien als spurenelementreiches Biogassubstrat; Berichte aus dem TFZ.; Technologie und Förderzentrum im Kompetenzzentrum für Nachwachsende Rohstoffe: Straubing, Germany, 2014; p. 120. [Google Scholar]
  154. Benton, T.G.; Vickery, J.A.; Wilson, J.D. Farmland biodiversity: Is habitat heterogeneity the key? Trends Ecol. Evol. 2003, 18, 182–188. [Google Scholar] [CrossRef]
  155. Viaud, V.; Durand, P.; Merot, P.; Sauboua, E.; Saadi, Z. Modeling the impact of the spatial structure of a hedge network on the hydrology of a small catchment in a temperate climate. Agric. Water Manag. 2005, 74, 135–163. [Google Scholar] [CrossRef]
  156. Dietzel, S.; Sauter, F.; Moosner, M.; Fischer, C.; Kollmann, J. Blühstreifen und Blühflächen in der landwirt-schaftlichen Praxis–eine naturschutzfach-liche Evaluation. Anliegen Nat. 2019, 41, 73–86. [Google Scholar]
  157. Pugesgaard, S.; Schelde, K.; Larsen, S.U.; Lærke, P.E.; Jørgensen, U. Comparing annual and perennial crops for bioenergy production–influence on nitrate leaching and energy balance. GCB Bioenergy 2015, 7, 1136–1149. [Google Scholar] [CrossRef]
  158. Ruf, T.; Makselon, J.; Udelhoven, T.; Emmerling, C. Soil quality indicator response to land-use change from annual to perennial bioenergy cropping systems in Germany. GCB Bioenergy 2018, 10, 444–459. [Google Scholar] [CrossRef]
  159. Muylle, H.; Van Hulle, S.; De Vliegher, A.; Baert, J.; Van Bockstaele, E.; Roldán-Ruiz, I. Yield and energy balance of annual and perennial lignocellulosic crops for bio-refinery use: A 4-year field experiment in Belgium. Eur. J. Agron. 2015, 63, 62–70. [Google Scholar] [CrossRef]
  160. Bradley, B.A.; Oppenheimer, M.; Wilcove, D.S. Climate change and plant invasions: Restoration opportunities ahead? Glob. Change Biol. 2009, 15, 1511–1521. [Google Scholar] [CrossRef]
  161. Biala, K.; Terres, J.-M.; Pointereau, P.; Paracchini, M.L. Low Input Farming Systems: An opportunity to develop sustainable agriculture. Proc. JRC Summer Univ. Ranco 2007, 2–5. Available online: https://ec.europa.eu/jrc/en/publication/eur-scientific-and-technical-research-reports/low-input-farming-systems-opportunity-develop-sustainable-agriculture-proceedings-jrc-summer (accessed on 1 October 2019).
  162. Pulighe, G.; Bonati, G.; Fabiani, S.; Barsali, T.; Lupia, F.; Vanino, S.; Nino, P.; Arca, P.; Roggero, P.P. Assessment of the Agronomic Feasibility of Bioenergy Crop Cultivation on Marginal and Polluted Land: A GIS-Based Suitability Study from the Sulcis Area, Italy. Energies 2016, 9, 895. [Google Scholar] [CrossRef]
  163. Heaton, E.A.; Dohleman, F.G.; Long, S.P. Meeting US biofuel goals with less land: The potential of Miscanthus. Glob. Change Biol. 2008, 14, 2000–2014. [Google Scholar] [CrossRef]
  164. Kørup, K.; Lærke, P.E.; Baadsgaard, H.; Andersen, M.N.; Kristensen, K.; Münnich, C.; Didion, T.; Jensen, E.S.; Mårtensson, L.-M.; Jørgensen, U. Biomass production and water use efficiency in perennial grasses during and after drought stress. GCB Bioenergy 2018, 10, 12–27. [Google Scholar] [CrossRef]
  165. Himken, M.; Lammel, J.; Neukirchen, D.; Czypionka-Krause, U.; Olfs, H.-W. Cultivation of Miscanthus under West European conditions: Seasonal changes in dry matter production, nutrient uptake and remobilization. Plant Soil 1997, 189, 117–126. [Google Scholar] [CrossRef]
  166. Arthurson, V.; Jäderlund, L. Utilization of natural farm resources for promoting high energy efficiency in low-input organic farming. Energies 2011, 4, 804–817. [Google Scholar] [CrossRef]
  167. Behnke, G.D.; Pittelkow, C.M.; Nafziger, E.D.; Villamil, M.B. Exploring the Relationships between Greenhouse Gas Emissions, Yields, and Soil Properties in Cropping Systems. Agriculture 2018, 8, 62. [Google Scholar] [CrossRef]
  168. Felten, D.; Fröba, N.; Fries, J.; Emmerling, C. Energy balances and greenhouse gas-mitigation potentials of bioenergy cropping systems (Miscanthus, rapeseed, and maize) based on farming conditions in Western Germany. Renew. Energy 2013, 55, 160–174. [Google Scholar] [CrossRef]
  169. Huang, Y.; Ren, W.; Wang, L.; Hui, D.; Grove, J.H.; Yang, X.; Tao, B.; Goff, B. Greenhouse gas emissions and crop yield in no-tillage systems: A meta-analysis. Agric. Ecosyst. Environ. 2018, 268, 144–153. [Google Scholar] [CrossRef]
  170. Hudiburg, T.W.; Davis, S.C.; Parton, W.; Delucia, E.H. Bioenergy crop greenhouse gas mitigation potential under a range of management practices. GCB Bioenergy 2015, 7, 366–374. [Google Scholar] [CrossRef]
  171. Jablonowski, N.D.; Kollmann, T.; Nabel, M.; Damm, T.; Klose, H.; Müller, M.; Bläsing, M.; Seebold, S.; Krafft, S.; Kuperjans, I.; et al. Valorization of Sida (Sida hermaphrodita) biomass for multiple energy purposes. GCB Bioenergy 2017, 9, 202–214. [Google Scholar] [CrossRef]
  172. Plaza-Bonilla, D.; Nolot, J.-M.; Raffaillac, D.; Justes, E. Cover crops mitigate nitrate leaching in cropping systems including grain legumes: Field evidence and model simulations. Agric. Ecosyst. Environ. 2015, 212, 1–12. [Google Scholar] [CrossRef]
  173. Thilakarathna, M.S.; Raizada, M.N. Challenges in using precision agriculture to optimize symbiotic nitrogen fixation in legumes: Progress, limitations, and future improvements needed in diagnostic testing. Agronomy 2018, 8, 78. [Google Scholar] [CrossRef]
  174. De Groot, R.S.; Wilson, M.A.; Boumans, R.M. A typology for the classification, description and valuation of ecosystem functions, goods and services. Ecol. Econ. 2002, 41, 393–408. [Google Scholar] [CrossRef] [Green Version]
  175. De Groot, R.; Brander, L.; Van Der Ploeg, S.; Costanza, R.; Bernard, F.; Braat, L.; Christie, M.; Crossman, N.; Ghermandi, A.; Hein, L. Global estimates of the value of ecosystems and their services in monetary units. Ecosyst. Serv. 2012, 1, 50–61. [Google Scholar] [CrossRef]
  176. Braat, L.C.; De Groot, R. The ecosystem services agenda: Bridging the worlds of natural science and economics, conservation and development, and public and private policy. Ecosyst. Serv. 2012, 1, 4–15. [Google Scholar] [CrossRef]
  177. Vaneeckhaute, C.; Lebuf, V.; Michels, E.; Belia, E.; Vanrolleghem, P.A.; Tack, F.M.G.; Meers, E. Nutrient Recovery from Digestate: Systematic Technology Review and Product Classification. Waste Biomass Valorization 2017, 8, 21–40. [Google Scholar] [CrossRef]
  178. KTBL Web-Anwendungen. Kuratorium für Technik und Bauwesen in der Landwirtschaft e.V., Darmstadt, Germany. 2019. Available online: https://www.ktbl.de/webanwendungen/ (accessed on 22 July 2019).
  179. Ehmann, A.; Bach, I.-M.; Laopeamthong, S.; Bilbao, J.; Lewandowski, I. Can phosphate salts recovered from manure replace conventional phosphate fertilizer? Agriculture 2017, 7, 1. [Google Scholar] [CrossRef]
  180. Monlau, F.; Sambusiti, C.; Ficara, E.; Aboulkas, A.; Barakat, A.; Carrère, H. New opportunities for agricultural digestate valorization: Current situation and perspectives. Energy Environ. Sci. 2015, 8, 2600–2621. [Google Scholar] [CrossRef]
  181. Bergfeldt, B.; Morgano, M.T.; Leibold, H.; Richter, F.; Stapf, D. Recovery of phosphorus and other nutrients during pyrolysis of chicken manure. Agriculture 2018, 8, 187. [Google Scholar] [CrossRef]
  182. Bilandžija, N.; Krička, T.; Matin, A.; Leto, J.; Grubor, M. Effect of Harvest Season on the Fuel Properties of Sida hermaphrodita (L.) Rusby Biomass as Solid Biofuel. Energies 2018, 11, 3398. [Google Scholar] [CrossRef]
  183. Nabel, M.; Schrey, S.D.; Poorter, H.; Koller, R.; Jablonowski, N.D. Effects of digestate fertilization on Sida hermaphrodita: Boosting biomass yields on marginal soils by increasing soil fertility. Biomass Bioenergy 2017, 107, 207–213. [Google Scholar] [CrossRef]
  184. Ceotto, E.; Marchetti, R.; Castelli, F. Residual soil nitrate as affected by giant reed cultivation and cattle slurry fertilisation. Ital. J. Agron. 2018, 13, 317–323. [Google Scholar]
  185. Ehmann, A.; Thumm, U.; Lewandowski, I. Fertilizing Potential of Separated Biogas Digestates in Annual and Perennial Biomass Production Systems. Front. Sustain. Food Syst. 2018, 2, 12. [Google Scholar] [CrossRef]
  186. Costa, J.; Barbosa, B.; Fernando, A.L. Wastewaters Reuse for Energy Crops Cultivation. In Technological Innovation for Cyber-Physical Systems; DoCEIS, IFIP Advances in Information and Communication Technology; Camarinha-Matos, L.M., Falcão, A.J., Vafaei, N., Najdi, S., Eds.; Springer: Cham, Switzerland, 2016; Volume 470, pp. 507–514. [Google Scholar]
  187. De Laporte, A.V.; Ripplinger, D.G. Economic viability of perennial grass biomass feedstock in northern climates. Ind. Crops Prod. 2019, 128, 213–220. [Google Scholar] [CrossRef]
  188. Cosentino, S.L.; Copani, V.; Scalici, G.; Scordia, D.; Testa, G. Soil erosion mitigation by perennial species under Mediterranean environment. BioEnergy Res. 2015, 8, 1538–1547. [Google Scholar] [CrossRef]
  189. Schulte, L.A.; Asbjornsen, H.; Liebman, M.; Crow, T.R. Agroecosystem restoration through strategic integration of perennials. J. Soil Water Conserv. 2006, 61, 164A–169A. [Google Scholar]
  190. Jankauskas, B.; Jankauskiene, G. Erosion-preventive crop rotations for landscape ecological stability in upland regions of Lithuania. Agric. Ecosyst. Environ. 2003, 95, 129–142. [Google Scholar] [CrossRef]
  191. Lewandowski, I.; Schmidt, U. Nitrogen, energy and land use efficiencies of miscanthus, reed canary grass and triticale as determined by the boundary line approach. Agric. Ecosyst. Environ. 2006, 112, 335–346. [Google Scholar] [CrossRef] [Green Version]
  192. Felten, D.; Emmerling, C. Effects of bioenergy crop cultivation on earthworm communities—A comparative study of perennial (Miscanthus) and annual crops with consideration of graded land-use intensity. Appl. Soil Ecol. 2011, 49, 167–177. [Google Scholar] [CrossRef]
  193. Zan, C.S.; Fyles, J.W.; Girouard, P.; Samson, R.A. Carbon sequestration in perennial bioenergy, annual corn and uncultivated systems in southern Quebec. Agric. Ecosyst. Environ. 2001, 86, 135–144. [Google Scholar] [CrossRef]
  194. Bonin, C.L.; Fidel, R.B.; Banik, C.; Laird, D.A.; Mitchell, R.; Heaton, E.A. Perennial biomass crop establishment, community characteristics, and productivity in the upper US Midwest: Effects of cropping systems seed mixtures and biochar applications. Eur. J. Agron. 2018, 101, 121–128. [Google Scholar] [CrossRef] [Green Version]
  195. Fernando, A.L.; Rettenmaier, N.; Soldatos, P.; Panoutsou, C. Sustainability of Perennial Crops Production for Bioenergy and Bioproducts. In Perennial Grasses for Bioenergy and Bioproducts; Alexopoulou, E., Ed.; Academic Press: Cambridge, MA, USA, 2018; pp. 245–283. [Google Scholar]
  196. Alexopoulou, E.; Zanetti, F.; Papazoglou, E.G.; Christou, M.; Papatheohari, Y.; Tsiotas, K.; Papamichael, I. Long-term studies on switchgrass grown on a marginal area in Greece under different varieties and nitrogen fertilization rates. Ind. Crops Prod. 2017, 107, 446–452. [Google Scholar] [CrossRef]
  197. Rutz, D.; Ugalde, J.M.; Mergner, R.; Janssen, R.; Epp, C.; Leplus, A.; Bernard, J.; Eleftheriadis, I.; Žandeckis, A.; Fištre, Ž.; et al. Short Rotation Woody Crops: Experiences from the eu Project Srcplus, Proceedings of the 25th European Biomass Conference and Exhibition; 25th European Biomass Conference and Exhibition: Stockholm, Sweden, 2017; pp. 143–149. [Google Scholar]
  198. McElroy, G.H.; Dawson, W.M. Biomass from short-rotation coppice willow on marginal land. Biomass 1986, 10, 225–240. [Google Scholar] [CrossRef]
  199. Wang, W.; Xie, Y.; Bi, M.; Wang, X.; Lu, Y.; Fan, Z. Effects of best management practices on nitrogen load reduction in tea fields with different slope gradients using the SWAT model. Appl. Geogr. 2018, 90, 200–213. [Google Scholar] [CrossRef]
  200. Vatsa, D.K.; Vyas, N. Modern farm technologies for enhancing work productivity with reduced drudgery of rural women in hill agriculture. AMA Agric. Mech. Asia Afr. Lat. Am. 2018, 49, 32–38. [Google Scholar]
  201. Pari, L.; Alfano, V.; Garcia-Galindo, D.; Suardi, A.; Santangelo, E. Pruning biomass potential in Italy related to crop characteristics, agricultural practices and agro-climatic conditions. Energies 2018, 11, 1365. [Google Scholar] [CrossRef]
  202. Cosentino, S.L.; Patanè, C.; Sanzone, E.; Testa, G.; Scordia, D. Leaf gas exchange, water status and radiation use efficiency of giant reed (Arundo donax L.) in a changing soil nitrogen fertilization and soil water availability in a semi-arid Mediterranean area. Eur. J. Agron. 2016, 72, 56–69. [Google Scholar] [CrossRef]
  203. Flexas, J.; DIAZ-ESPEJO, A.; GalmES, J.; Kaldenhoff, R.; Medrano, H.; RIBAS-CARBO, M. Rapid variations of mesophyll conductance in response to changes in CO2 concentration around leaves. Plant Cell Environ. 2007, 30, 1284–1298. [Google Scholar] [CrossRef] [PubMed]
  204. Lawlor, D.W.; Cornic, G. Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ. 2002, 25, 275–294. [Google Scholar] [CrossRef] [Green Version]
  205. Sánchez, E.; Scordia, D.; Lino, G.; Arias, C.; Cosentino, S.L.; Nogués, S. Salinity and water stress effects on biomass production in different Arundo donax L. clones. BioEnergy Res. 2015, 8, 1461–1479. [Google Scholar] [CrossRef]
  206. Van Orshoven, J.; Terres, J.-M.; Tóth, T. Updated common bio-physical criteria to define natural constraints for agriculture in Europe—Definition and scientific justification for the common biophysical criteria. JRC Sci. Policy Rep. 2014. [Google Scholar]
  207. Terres, J.-M.; Hagyo, A.; Wania, A. Scientific contribution on combining biophysical criteria underpinning the delineation of agricultural areas affected by specific constraints: Methodology and factsheets for plausible criteria combinations. JRC Sci. Policy Rep. 2014. Available online: https://ec.europa.eu/jrc/en/publication/eur-scientific-and-technical-research-reports/scientific-contribution-combining-biophysical-criteria-underpinning-delineation-agricultural (accessed on 1 October 2019).
  208. Volaire, F.; Barkaoui, K.; Norton, M. Designing resilient and sustainable grasslands for a drier future: Adaptive strategies, functional traits and biotic interactions. Eur. J. Agron. 2014, 52, 81–89. [Google Scholar] [CrossRef] [Green Version]
  209. Cosentino, S.L.; Scordia, D.; Sanzone, E.; Testa, G.; Copani, V. Response of giant reed (Arundo donax L.) to nitrogen fertilization and soil water availability in semi-arid Mediterranean environment. Eur. J. Agron. 2014, 60, 22–32. [Google Scholar] [CrossRef]
  210. Lelièvre, F.; Seddaiu, G.; Ledda, L.; Porqueddu, C.; Volaire, F. Water use efficiency and drought survival in Mediterranean perennial forage grasses. Field Crops Res. 2011, 121, 333–342. [Google Scholar] [CrossRef]
  211. Fernando, A.L. Environmental Aspects of Kenaf Production and Use. In Kenaf: A Multi-Purpose Crop for Several Industrial Applications: New insights from the Biokenaf Project; Monti, A., Alexopoulou, E., Eds.; Springer: London, UK, 2013; pp. 83–104. [Google Scholar]
  212. Reynolds, W.D.; Bowman, B.T.; Drury, C.F.; Tan, C.S.; Lu, X. Indicators of good soil physical quality: Density and storage parameters. Geoderma 2002, 110, 131–146. [Google Scholar] [CrossRef]
  213. Von Cossel, M.; Iqbal, Y.; Scordia, D.; Cosentino, S.L.; Elbersen, B.; Staritsky, I.; Van Eupen, M.; Mantel, S.; Prysiazhniuk, O.; Maliarenko, O.; et al. Low-Input Agricultural Practices for Industrial Crops on Marginal Land. EU-Deliverable; University of Hohenheim: Stuttgart, Germany, 2018. [Google Scholar]
  214. Ruf, T.; Audu, V.; Holzhauser, K.; Emmerling, C. Bioenergy from periodically waterlogged cropland in Europe: A first assessment of the potential of five perennial energy crops to provide biomass and their interactions with soil. Agronomy 2019, 9, 374. [Google Scholar] [CrossRef]
  215. Van Orshoven, J.; Terres, J.-M.; Tóth, T. Updated common bio-physical criteria to define natural constraints for agriculture in Europe. JRC Sci. Tech. Rep. 2012. Available online: https://www.semanticscholar.org/paper/Updated-common-bio-physical-criteria-to-define-for-Jos-Jean/1176dee267e586b47dd45be6c568dd6312990735 (accessed on 1 October 2019).
  216. Obia, A.; Mulder, J.; Hale, S.E.; Nurida, N.L.; Cornelissen, G. The potential of biochar in improving drainage, aeration and maize yields in heavy clay soils. PLoS ONE 2018, 13, e0196794. [Google Scholar] [CrossRef] [PubMed]
  217. Rasmussen, K.J. Impact of ploughless soil tillage on yield and soil quality: A Scandinavian review. Soil Tillage Res. 1999, 53, 3–14. [Google Scholar] [CrossRef]
  218. Kharytonov, M.; Pidlisnyuk, V.; Stefanovska, T.; Babenko, M.; Martynova, N.; Rula, I. The estimation of Miscanthus×giganteus’ adaptive potential for cultivation on the mining and post-mining lands in Ukraine. Environ. Sci. Pollut. Res. 2019, 26, 2974–2986. [Google Scholar] [CrossRef]
  219. Lamb, D.T.; Heading, S.; Bolan, N.; Naidu, R. Use of biosolids for phytocapping of landfill soil. Water. Air. Soil Pollut. 2012, 223, 2695–2705. [Google Scholar] [CrossRef]
  220. Barbosa, B.; Fernando, A.L. Chapter 9 - Aided Phytostabilization of Mine Waste. In Bio-Geotechnologies for Mine Site Rehabilitation; Prasad, M.N.V., de Favas, P.J.C., Maiti, S.K., Eds.; Elsevier: Amsterdam, The Netherlands, 2018; pp. 147–157. [Google Scholar]
  221. Barbosa, B.; Costa, J.; Fernando, A.L. Production of Energy Crops in Heavy Metals Contaminated Land: Opportunities and Risks. In Land Allocation for Biomass Crops: Challenges and Opportunities with Changing Land Use; Li, R., Monti, A., Eds.; Springer International Publishing: Cham, Switzerland, 2018; pp. 83–102. [Google Scholar]
  222. The Council of the European Communities Council directive on the protection of the environment, and in particular of the soil, when sewage sludge is used in agriculture. Off. J. Eur. Comm. 1986, 181, 0006–0012.
  223. Barbosa, B.; Boléo, S.; Sidella, S.; Costa, J.; Duarte, M.P.; Mendes, B.; Cosentino, S.L.; Fernando, A.L. Phytoremediation of Heavy Metal-Contaminated Soils Using the Perennial Energy Crops Miscanthus spp. and Arundo donax L. BioEnergy Res. 2015, 8, 1500–1511. [Google Scholar] [CrossRef]
  224. Radojčić Redovniković, I.; De Marco, A.; Proietti, C.; Hanousek, K.; Sedak, M.; Bilandžić, N.; Jakovljević, T. Poplar response to cadmium and lead soil contamination. Ecotoxicol. Environ. Saf. 2017, 144, 482–489. [Google Scholar] [CrossRef] [PubMed]
  225. Pandey, V.C.; Bajpai, O.; Singh, N. Energy crops in sustainable phytoremediation. Renew. Sustain. Energy Rev. 2016, 54, 58–73. [Google Scholar] [CrossRef]
  226. Fernando, A.L.; Boléo, S.; Barbosa, B.; Costa, J.; Lino, J.; Tavares, C.; Sidella, S.; Duarte, M.P.; Mendes, B. How sustainable is the production of energy crops in heavy metal contaminated soils. In Proceedings of the 22th European Biomass Conference and Exhibition, Setting the Course for a Biobased Economy; ETA-Renewable Energies: Hamburg, Germany, 2014; pp. 1593–1596. [Google Scholar]
  227. Papazoglou, E.G.; Fernando, A.L. Preliminary studies on the growth, tolerance and phytoremediation ability of sugarbeet (Beta vulgaris L.) grown on heavy metal contaminated soil. Ind. Crops Prod. 2017, 107, 463–471. [Google Scholar] [CrossRef]
  228. Sidella, S.; Barbosa, B.; Costa, J.; Cosentino, S.L.; Fernando, A.L. Screening of Giant reed clones for Phytoremediation of lead contaminated soils. In Perennial Biomass Crops for a Resource-Constrained World; Barth, S., Murphy-Bokern, D., Kalinina, O., Taylor, G., Jones, M., Eds.; Springer: Berlin/Heidelberg, Germany, 2016; pp. 191–197. [Google Scholar]
  229. Fernando, A.L.; Godovikova, V.; Oliveira, J.F.S. Miscanthus x giganteus: Contribution to a sustainable agriculture of a future/present-oriented biomaterial. Trans. Tech. Publ. 2004, 455, 437–441. [Google Scholar] [CrossRef]
  230. Iqbal, Y.; Lewandowski, I. Inter-annual variation in biomass combustion quality traits over five years in fifteen Miscanthus genotypes in south Germany. Fuel Process. Technol. 2014, 121, 47–55. [Google Scholar] [CrossRef]
  231. Iqbal, Y.; Kiesel, A.; Wagner, M.; Nunn, C.; Kalinina, O.; Hastings, A.F.S.J.; Clifton-Brown, J.C.; Lewandowski, I. Harvest time optimization for combustion quality of different miscanthus genotypes across Europe. Front. Plant Sci. 2017, 8, 727. [Google Scholar] [CrossRef]
  232. Van der Weijde, T.; Kiesel, A.; Iqbal, Y.; Muylle, H.; Dolstra, O.; Visser, R.G.F.; Lewandowski, I.; Trindade, L.M. Evaluation of Miscanthus sinensis biomass quality as feedstock for conversion into different bioenergy products. GCB Bioenergy 2017, 9, 176–190. [Google Scholar] [CrossRef]
  233. Fernando, A.L.; Barbosa, B.; Costa, J.; Papazoglou, E.G. Giant reed (arundo donax l.): A multipurpose crop bridging phytoremediation with sustainable bioeconomy. In Bioremediation and Bioeconomy; Prasad, M.N.V., Ed.; Elsevier: Amsterdam, The Netherlands, 2016; pp. 77–95. [Google Scholar]
  234. Gomes, L.; Fernando, A.L.; Santos, F. A toolbox to tackle the technological and environmental constraints associated with the use of biomass for energy from marginal land. In Proceedings of the ECOS 2018, the 31st International Conference on Efficiency, Cost, Optimization, Simulation and Environmental Impact of Energy Systems, Guimarães, Portugal, 17–22 June 2018. [Google Scholar]
  235. Lomba, A.; Buchadas, A.; Honrado, J.P.; Moreira, F. Are We Missing the Big Picture? Unlocking the Social-Ecological Resilience of High Nature Value Farmlands to Future Climate Change. In Climate Change-Resilient Agriculture and Agroforestry; Castro, P., Azul, A.M., Leal Filho, W., Azeiteiro, U.M., Eds.; Springer: Berlin/Heidelberg, Germany, 2019; pp. 53–72. [Google Scholar]
  236. Tuck, G.; Glendining, M.J.; Smith, P.; House, J.I.; Wattenbach, M. The potential distribution of bioenergy crops in Europe under present and future climate. Biomass Bioenergy 2006, 30, 183–197. [Google Scholar] [CrossRef]
  237. Garbolino, E.; Daniel, W.; Hinojos Mendoza, G. Expected Global Warming Impacts on the Spatial Distribution and Productivity for 2050 of Five Species of Trees Used in the Wood Energy Supply Chain in France. Energies 2018, 11, 3372. [Google Scholar] [CrossRef]
  238. Samaniego, L.; Thober, S.; Kumar, R.; Wanders, N.; Rakovec, O.; Pan, M.; Zink, M.; Sheffield, J.; Wood, E.F.; Marx, A. Anthropogenic warming exacerbates European soil moisture droughts. Nat. Clim. Change 2018, 8, 421. [Google Scholar] [CrossRef]
  239. Teuling, A.J. A hot future for European droughts. Nat. Clim. Change 2018, 8, 364. [Google Scholar] [CrossRef]
  240. Giorgi, F.; Gutowski, W.J. Regional Dynamical Downscaling and the CORDEX Initiative. Annu. Rev. Environ. Resour. 2015, 40, 467–490. [Google Scholar] [CrossRef]
  241. Jacob, D.; Petersen, J.; Eggert, B.; Alias, A.; Christensen, O.B.; Bouwer, L.M.; Braun, A.; Colette, A.; Déqué, M.; Georgievski, G.; et al. EURO-CORDEX: New high-resolution climate change projections for European impact research. Reg. Environ. Change 2014, 14, 563–578. [Google Scholar] [CrossRef]
  242. Soares, P.M.M.; Cardoso, R.M.; Lima, D.C.A.; Miranda, P.M.A. Future precipitation in Portugal: High-resolution projections using WRF model and EURO-CORDEX multi-model ensembles. Clim. Dyn. 2017, 49, 2503–2530. [Google Scholar] [CrossRef]
  243. Pfeifer, S.; Bülow, K.; Gobiet, A.; Hänsler, A.; Mudelsee, M.; Otto, J.; Rechid, D.; Teichmann, C.; Jacob, D. Robustness of Ensemble Climate Projections Analyzed with Climate Signal Maps: Seasonal and Extreme Precipitation for Germany. Atmosphere 2015, 6, 677–698. [Google Scholar] [CrossRef] [Green Version]
  244. Huebener, H.; Hoffmann, P.; Keuler, K.; Pfeifer, S.; Ramthun, H.; Spekat, A.; Steger, C.; Warrach-Sagi, K. Deriving user-informed climate information from climate model ensemble results. Adv. Sci. Res. 2017, 14, 261–269. [Google Scholar] [CrossRef] [Green Version]
  245. Galatsidas, S.; Gounaris, N.; Vlachaki, D.; Dimitriadis, E.; Kiourtsis, F.; Keramitzis, D.; Gerwin, W.; Repmann, F.; Rettenmaier, N.; Reinhardt, G. Revealing Bioenergy Potentials: Mapping Marginal Lands in Europe—The SEEMLA Approach. In Proceedings of the 26th European Biomass Conference and Exhibition, Copenhagen, Denmark, 14–18 May 2018; pp. 31–37. [Google Scholar]
  246. Gerwin, W.; Repmann, F.; Galatsidas, S.; Vlachaki, D.; Gounaris, N.; Baumgarten, W.; Volkmann, C.; Keramitzis, D.; Kiourtsis, F.; Freese, D. Assessment and quantification of marginal lands for biomass production in Europe using soil-quality indicators. SOIL 2018, 4, 267–290. [Google Scholar] [CrossRef] [Green Version]
  247. IPCC, Global Warming of 1.5 °C. An IPCC Special Report on the impacts of global warming of 1.5 °C above pre-industrial levels and related global greenhouse gas emission pathways, in the context of strengthening the global response to the threat of climate change, sustainable development, and efforts to eradicate poverty [Masson-Delmotte, V., P. Zhai, H.-O. örtner, D. Roberts, J. Skea, P.R. Shukla, A. Pirani, W. Moufouma-Okia, C. Péan, R. Pidcock, S. Connors, J.B.R. Matthews, Y. Chen, X. Zhou, M.I. Gomis, E. Lonnoy, T. Maycock, M. Tignor, and T. Waterfield (eds.)]. 2018; in press.
  248. Sage, R.F.; Kubien, D.S. The temperature response of C3 and C4 photosynthesis. Plant Cell Environ. 2007, 30, 1086–1106. [Google Scholar] [CrossRef]
  249. Poorter, H.; Navas, M.-L. Plant growth and competition at elevated Co2: On winners, losers and functional groups. New Phytol. 2003, 157, 175–198. [Google Scholar] [CrossRef]
  250. Sage, R.F.; Sage, T.L. C4 Plants. In Encyclopedia of Biodiversity, 2nd ed.; Levin, S.A., Ed.; Academic Press: Waltham, MA, USA, 2013; pp. 361–381. [Google Scholar]
  251. Seneviratne, S.I.; Corti, T.; Davin, E.L.; Hirschi, M.; Jaeger, E.B.; Lehner, I.; Orlowsky, B.; Teuling, A.J. Investigating soil moisture–climate interactions in a changing climate: A review. Earth-Sci. Rev. 2010, 99, 125–161. [Google Scholar] [CrossRef]
  252. Weselek, A.; Ehmann, A.; Zikeli, S.; Lewandowski, I.; Schindele, S.; Högy, P. Agrophotovoltaic systems: Applications, challenges, and opportunities. A review. Agron. Sustain. Dev. 2019, 39, 35. [Google Scholar] [CrossRef]
  253. Amaducci, S.; Yin, X.; Colauzzi, M. Agrivoltaic systems to optimise land use for electric energy production. Appl. Energy 2018, 220, 545–561. [Google Scholar] [CrossRef]
  254. MAGIC Marginal Lands for Growing Industrial Crops: Turning a Burden into an Opportunity. 2019. Available online: http://magic-h2020.eu/ (accessed on 14 June 2019).
  255. Cai, H.; Wang, J.; Feng, Y.; Wang, M.; Qin, Z.; Dunn, J.B. Consideration of land use change-induced surface albedo effects in life-cycle analysis of biofuels. Energy Environ. Sci. 2016, 9, 2855–2867. [Google Scholar] [CrossRef] [Green Version]
  256. Möndel, A. Ertragsmessungen in Winterroggen-der Ertragseinfluss einer Windschutzanlage in der oberrheinischen Tiefebene. Verbundprojekt: agroforst - neue Optionen für eine nachhaltige Landnutzung, LAP Forchheim, Germany. 2007. Available online: http://docplayer.org/38193544-Ertragsmessungen-in-winterroggen-der-ertragseinfluss-einer-windschutzanlage-in-der-oberrheinischen-tiefebene.html (accessed on 1 October 2019).
  257. Goetsch, E.; Colinas, F.T. Natural succession of species in agroforestry and in soil recovery. 1992. Available online: media0.agrofloresta.net/static/artigos/agroforestry_1992_gotsch.pdf (accessed on 1 October 2019).
  258. FAO. Bioenergy and Food Security—The BEFS Analytical Framework; Environment and Natural Resources Management Series; Sales and Marketing Group—Communication Division Food and Agriculture Organization of the United Nations: Rome, Italy, 2010. [Google Scholar]
  259. Kaygusuz, K. Energy for sustainable development: A case of developing countries. Renew. Sustain. Energy Rev. 2012, 16, 1116–1126. [Google Scholar] [CrossRef]
  260. Winkler, B.; Lewandowski, I.; Voss, A.; Lemke, S. Transition towards Renewable Energy Production? Potential in Smallholder Agricultural Systems in West Bengal, India. Sustainability 2018, 10, 801. [Google Scholar] [CrossRef]
  261. FAO. Evidence-Based Assessment of the Sustainability and Replicability of Integrated Food-Energy Systems—A Guidance Document; Environment and Natural Resources Working Paper; Sales and Marketing Group—Communication Division Food and Agriculture Organization of the United Nations: Rome, Italy, 2014. [Google Scholar]
  262. Chen, R. Livestock-biogas-fruit systems in South China. Ecol. Eng. 1997, 8, 19–29. [Google Scholar] [CrossRef]
  263. Gu, L.; Zhang, Y.-X.; Wang, J.-Z.; Chen, G.; Battye, H. Where is the future of China’s biogas? Review, forecast, and policy implications. Pet. Sci. 2016, 13, 604–624. [Google Scholar] [CrossRef]
  264. MNRE National Biogas and Manure Management Programme. 2019. Available online: https://mnre.gov.in/biogas (accessed on 8 August 2019).
  265. Amigun, B.; Musango, J.K.; Brent, A.C. Community perspectives on the introduction of biodiesel production in the Eastern Cape Province of South Africa. Energy 2011, 36, 2502–2508. [Google Scholar] [CrossRef]
  266. Barry, M.-L.; Steyn, H.; Brent, A. Selection of renewable energy technologies for Africa: Eight case studies in Rwanda, Tanzania and Malawi. Renew. Energy 2011, 36, 2845–2852. [Google Scholar] [CrossRef] [Green Version]
  267. Brent, A.C.; Kruger, W.J.L. Systems analyses and the sustainable transfer of renewable energy technologies: A focus on remote areas of Africa. Renew. Energy 2009, 34, 1774–1781. [Google Scholar] [CrossRef] [Green Version]
  268. Duku, M.H.; Gu, S.; Hagan, E.B. A comprehensive review of biomass resources and biofuels potential in Ghana. Renew. Sustain. Energy Rev. 2011, 15, 404–415. [Google Scholar] [CrossRef]
  269. Practical Action Consulting. Small-Scale Bioenergy Initiatives: Brief Description and Preliminary Lessons on Livelihood Impacts from Case Studies in Asia, Latin America and Africa; Practical Action Consulting, Food and Agriculture Organization of the United Nations, Climate Change and Bioenergy Unit: Rome, Italy, 2009. [Google Scholar]
  270. Stoknes, K.; Scholwin, F.; Krzesiński, W.; Wojciechowska, E.; Jasińska, A. Efficiency of a novel “Food to waste to food” system including anaerobic digestion of food waste and cultivation of vegetables on digestate in a bubble-insulated greenhouse. Waste Manag. 2016, 56, 466–476. [Google Scholar] [CrossRef] [PubMed]
  271. Kloepffer, W. Life cycle sustainability assessment of products. Int. J. Life Cycle Assess. 2008, 13, 89. [Google Scholar] [CrossRef]
  272. Fernando, A.L.; Costa, J.; Barbosa, B.; Monti, A.; Rettenmaier, N. Environmental impact assessment of perennial crops cultivation on marginal soils in the Mediterranean Region. Biomass Bioenergy 2018, 111, 174–186. [Google Scholar] [CrossRef]
  273. Wagner, M.; Kiesel, A.; Hastings, A.; Iqbal, Y.; Lewandowski, I. Novel miscanthus germplasm-based value chains: A Life Cycle Assessment. Front. Plant Sci. 2017, 8, 990. [Google Scholar] [CrossRef]
  274. Meyer, S.T.; Ebeling, A.; Eisenhauer, N.; Hertzog, L.; Hillebrand, H.; Milcu, A.; Pompe, S.; Abbas, M.; Bessler, H.; Buchmann, N. Effects of biodiversity strengthen over time as ecosystem functioning declines at low and increases at high biodiversity. Ecosphere 2016, 7, e01619. [Google Scholar] [CrossRef]
  275. Schmidt, T.; Fernando, A.L.; Monti, A.; Rettenmaier, N. Life Cycle Assessment of Bioenergy and Bio-Based Products from Perennial Grasses Cultivated on Marginal Land in the Mediterranean Region. BioEnergy Res. 2015, 8, 1548–1561. [Google Scholar] [CrossRef]
  276. De Laurentiis, V.; Secchi, M.; Bos, U.; Horn, R.; Laurent, A.; Sala, S. Soil quality index: Exploring options for a comprehensive assessment of land use impacts in LCA. J. Clean. Prod. 2019, 215, 63–74. [Google Scholar] [CrossRef]
  277. Winter, L.; Lehmann, A.; Finogenova, N.; Finkbeiner, M. Including biodiversity in life cycle assessment—State of the art, gaps and research needs. Environ. Impact Assess. Rev. 2017, 67, 88–100. [Google Scholar] [CrossRef]
  278. Brankatschk, G.; Finkbeiner, M. Crop rotations and crop residues are relevant parameters for agricultural carbon footprints. Agron. Sustain. Dev. 2017, 37, 58. [Google Scholar] [CrossRef] [Green Version]
  279. EEX European Emission Allowances (EUA). 2019. Available online: https://www.eex.com/en/market-data/environmental-markets/spot-market/european-emission-allowances (accessed on 21 July 2019).
  280. Matthey, A.; Bünger, B. Methodenkonvention 3.0 zur Ermittlung von Umweltkosten Kostensätze Stand 02/2019; Für Mensch und Umwelt; Umweltbundesamt: Dessau-Rosslau, Germany, 2019. [Google Scholar]
  281. Landis, D.A.; Gratton, C.; Jackson, R.D.; Gross, K.L.; Duncan, D.S.; Liang, C.; Meehan, T.D.; Robertson, B.A.; Schmidt, T.M.; Stahlheber, K.A. Biomass and biofuel crop effects on biodiversity and ecosystem services in the North Central US. Biomass Bioenergy 2018, 114, 18–29. [Google Scholar] [CrossRef]
  282. Breeze, T.D.; Gallai, N.; Garibaldi, L.A.; Li, X.S. Economic Measures of Pollination Services: Shortcomings and Future Directions. Trends Ecol. Evol. 2016, 31, 927–939. [Google Scholar] [CrossRef] [PubMed]
  283. Williams, N.M.; Ward, K.L.; Pope, N.; Isaacs, R.; Wilson, J.; May, E.A.; Ellis, J.; Daniels, J.; Pence, A.; Ullmann, K.; et al. Native wildflower plantings support wild bee abundance and diversity in agricultural landscapes across the United States. Ecol. Appl. 2015, 25, 2119–2131. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  284. Pizzol, M.; Weidema, B.; Brandão, M.; Osset, P. Monetary valuation in Life Cycle Assessment: A review. J. Clean. Prod. 2015, 86, 170–179. [Google Scholar] [CrossRef]
  285. Hastings, A.; Mos, M.; Yesufu, J.A.; McCalmont, J.; Schwarz, K.; Shafei, R.; Ashman, C.; Nunn, C.; Schuele, H.; Cosentino, S.; et al. Economic and Environmental Assessment of Seed and Rhizome Propagated Miscanthus in the UK. Front. Plant Sci. 2017, 8, 1058. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  286. Huth, E.; Paltrinieri, S.; Thiele, J. Bioenergy and its effects on landscape aesthetics–A survey contrasting conventional and wild crop biomass production. Biomass Bioenergy 2019, 122, 313–321. [Google Scholar] [CrossRef]
  287. Finkbeiner, M.; Schau, E.M.; Lehmann, A.; Traverso, M. Towards Life Cycle Sustainability Assessment. Sustainability 2010, 2, 3309–3322. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Impressions of some promising bioenergy/multi-purpose crops and their inflorescences: (a) yellow melilot (Melilotus officinalis L.) as part of a wild plant mixture for biogas production (‘BG90’, Saaten Zeller GmbH & Co. KG, Eichenbühl, Germany), (b) camelina (Camelina sativa L. Crantz), (c) hemp (Cannabis sativa L.), (d) cup plant (Silphium perfoliatum L.), (e) Virginia mallow (Sida hermaphrodita L. Rusby), and (f) miscanthus (Miscanthus × giganteus Greef et Deuter).
Figure 1. Impressions of some promising bioenergy/multi-purpose crops and their inflorescences: (a) yellow melilot (Melilotus officinalis L.) as part of a wild plant mixture for biogas production (‘BG90’, Saaten Zeller GmbH & Co. KG, Eichenbühl, Germany), (b) camelina (Camelina sativa L. Crantz), (c) hemp (Cannabis sativa L.), (d) cup plant (Silphium perfoliatum L.), (e) Virginia mallow (Sida hermaphrodita L. Rusby), and (f) miscanthus (Miscanthus × giganteus Greef et Deuter).
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Figure 2. Mono-cropped maize (Zea mays L.) in Hohenheim (a) and Sankt Johann (b), Southwest Germany, August 2019.
Figure 2. Mono-cropped maize (Zea mays L.) in Hohenheim (a) and Sankt Johann (b), Southwest Germany, August 2019.
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Figure 3. Factors and mechanisms potentially determining agronomic effects of agricultural diversification of bioenergy cropping systems both between (brown boxes) and within the plant stands (green boxes) (adapted from [109]). Note, that the agronomic effects (grey box) show the potential outcome for a best-case scenario.
Figure 3. Factors and mechanisms potentially determining agronomic effects of agricultural diversification of bioenergy cropping systems both between (brown boxes) and within the plant stands (green boxes) (adapted from [109]). Note, that the agronomic effects (grey box) show the potential outcome for a best-case scenario.
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Figure 4. Current distribution of marginal agricultural land (ANC: agricultural natural constraint. Sub-severe ANC + 20% is within the 20% margin of the threshold value of severity) in Europe (adapted from [51]).
Figure 4. Current distribution of marginal agricultural land (ANC: agricultural natural constraint. Sub-severe ANC + 20% is within the 20% margin of the threshold value of severity) in Europe (adapted from [51]).
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Figure 5. Current (years 1970–2000) (a) and projected (years 2070–2100) (b) thermal time (in growth degree days, GDD) under the RCP8.5 scenario in Europe. The base temperature is set at 10 °C which applies to the requirements of C4-crops such as miscanthus (Miscanthus × giganteus Greef et Deuter) and maize (Zea mays L.).
Figure 5. Current (years 1970–2000) (a) and projected (years 2070–2100) (b) thermal time (in growth degree days, GDD) under the RCP8.5 scenario in Europe. The base temperature is set at 10 °C which applies to the requirements of C4-crops such as miscanthus (Miscanthus × giganteus Greef et Deuter) and maize (Zea mays L.).
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Figure 6. Projected changes in precipitation during the seasons March–May (a) and September – November (b) until 2050 given a RCP8.5 scenario. Data based on EC-EARTH–CCLM output.
Figure 6. Projected changes in precipitation during the seasons March–May (a) and September – November (b) until 2050 given a RCP8.5 scenario. Data based on EC-EARTH–CCLM output.
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Figure 7. Household biodigester (a) Deenbandhu Model: (1) inlet filled with manure and water; (2) underground fixed-dome fermenter, and (3) outlet chamber in the rural village of Ghoragachha, West Bengal India. (b). Women cooking on a biogas stove, directly connected with the biodigester.
Figure 7. Household biodigester (a) Deenbandhu Model: (1) inlet filled with manure and water; (2) underground fixed-dome fermenter, and (3) outlet chamber in the rural village of Ghoragachha, West Bengal India. (b). Women cooking on a biogas stove, directly connected with the biodigester.
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Von Cossel, M.; Wagner, M.; Lask, J.; Magenau, E.; Bauerle, A.; Von Cossel, V.; Warrach-Sagi, K.; Elbersen, B.; Staritsky, I.; Van Eupen, M.; et al. Prospects of Bioenergy Cropping Systems for A More Social-Ecologically Sound Bioeconomy. Agronomy 2019, 9, 605. https://doi.org/10.3390/agronomy9100605

AMA Style

Von Cossel M, Wagner M, Lask J, Magenau E, Bauerle A, Von Cossel V, Warrach-Sagi K, Elbersen B, Staritsky I, Van Eupen M, et al. Prospects of Bioenergy Cropping Systems for A More Social-Ecologically Sound Bioeconomy. Agronomy. 2019; 9(10):605. https://doi.org/10.3390/agronomy9100605

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Von Cossel, Moritz, Moritz Wagner, Jan Lask, Elena Magenau, Andrea Bauerle, Viktoria Von Cossel, Kirsten Warrach-Sagi, Berien Elbersen, Igor Staritsky, Michiel Van Eupen, and et al. 2019. "Prospects of Bioenergy Cropping Systems for A More Social-Ecologically Sound Bioeconomy" Agronomy 9, no. 10: 605. https://doi.org/10.3390/agronomy9100605

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