Ideas and perspectives: Synergies from co-deployment of negative emission technologies
- Institute for Geology, Center for Earth System Research and Sustainability, Universität Hamburg, Germany
Correspondence: Thorben Amann (email@example.com)
Numerous publications propose the deployment of negative emission technologies, which intend to actively remove CO2 from the atmosphere with the goal to reach the 1.5∘ target as discussed by the IPCC. The increasing number of scientific studies on the individual potential of different envisaged technologies and methods indicates that no single method has enough capacities to mitigate the issue by itself. It is thus expected that technology portfolios are deployed. As some of them utilize the same environmental compartment, co-deployment effects are expected. Those effects are particularly important to evaluate with respect to additional CO2 uptake. Considering soils as one of the main affected compartments, we see a plethora of processes which can positively benefit from each other, canceling out negative side effects or increasing overall CO2 sequestration potentials. To derive more reliable estimates of negative emission potentials and to evaluate common effects on global carbon pools, it is now necessary to intensively study interrelated effects of negative emission technology deployment while minimizing negative side effects.
As global mean temperatures are projected to increase further, strategies to mitigate climate change in time by decreasing CO2 emissions seem to slowly take effect (Jackson et al., 2015). Some CO2 emission pathways include negative carbon emission strategies (Fuss et al., 2014, 2016; Rogelj et al., 2018) that essentially capture CO2 from the atmosphere in different ways, storing them in the long term as CO2 molecules, or as organic and inorganic compounds (Caldeira et al., 2013). All discussed options and technologies have yet to reach the large-scale deployment stage (Minx et al., 2018; Nemet et al., 2018). Most technologies are immature, lacking deep research on the global potential, technical feasibility, economics of deployment, and especially an assessment of the expected side effects (National Research Council, 2015; Fuss et al., 2018).
The proposed negative emission technologies (NETs) encompass highly technical engineering solutions as well as methods that rely on natural processes, like growth of biomass (e.g., bioenergy with carbon capture and storage (BECCS), and afforestation), soil carbon increase, biochar, and chemical weathering (e.g., Enhanced Weathering (EW) and ocean liming). As these methods are aimed to be integrated in global biogeochemical cycles and will redistribute carbon between reservoirs (Keller et al., 2018), their interaction is inevitable if NETs are deployed at the largest scale. As such, it must be assessed how the co-deployment of NETs will affect the individual and overall efficiency since until now publications have focussed generally on single NETs, disregarding any effects on concurrent deployment of additional technologies.
Findings from NET-specific literature suggest that assessing the effects of combined NET rollout is advisable and future research should include CO2-sequestration-enhancing side effects that could increase the overall potential of NETs. However, the principal interaction between proposed methods needs to be studied in detail beforehand to understand effects on the carbon pools (Fig. 1).
While biomass-based NETs like afforestation and BECCS are widely discussed, EW is underrepresented in this discussion (Minx et al., 2018). EW relies on the uptake of CO2 via dissolution of minerals based on the natural process of chemical weathering. EW is facilitated by the application of finely ground rock on (agricultural) land, preferably in areas with elevated temperatures and rainfall. The resources for this NET have to be mined and, depending on the type and scale of rollout, the extraction of material can result in the creation of extensive mining areas. However, under a sustainable approach, affected environments could later be used to create biodiversity hotspots (e.g., Tropek et al., 2010; Benes et al., 2003).
It is unavoidable that the intended CO2 sequestration effect by weathering is naturally accompanied by the release of elements with consequences for the environment (Kantola et al., 2017) and consequently the involved carbon pools. The release of elements that are important plant nutrients (e.g., potassium, phosphorus, magnesium) can be beneficial for additional CO2 sequestration via organic carbon formation. In addition, the soil hydrology can be improved, and cation exchange capacity increased under optimal grain size distribution and mineral selection. In contrast, effects of potentially harmful trace element release (by choosing less suitable material) might need to be alleviated. However, an integrated framework to achieve optimization of interrelated effects between land-based NETs has yet to be developed, specifically for the global-scale management of carbon pools.
To tackle the issue of climate change with negative carbon emission strategies on a global and comprehensive scale, it seems advisable to consider all proposed terrestrial biomass-based NETs, like BECSS, afforestation, and biochar, to explore synergistic effects (Fig. 1). A scenario can be envisioned, in which rock powder and biochar are applied to agricultural land, which is used for bioenergy plant production (for further use in BECSS technology). Rock material would release geogenic nutrients and biochar could enhance the release of nutrients (Atkinson et al., 2010) and the overall crop productivity (Jeffery et al., 2011).
In combination with envisioned and deployed afforestation efforts, which often take place in tropical areas with depleted soils (Nilsson and Schopfhauser, 1995; Grainger, 1988; Zomer et al., 2008), rock powder deployment for EW could be an added, if not essential, benefit. The low capacity of these soils to retain highly soluble industrial fertilizers suggests the use of other forms of slow release fertilizer, like rock dust as a complement (Leonardos et al., 1987; Manning, 2015), or new emerging rock-based fertilizers (Ciceri and Allanore, 2019), which can, as a side effect, increase the retention of industrial fertilizers, which may still be needed. The ultimate need for an intense management and design of a suitable soil to supply suitable conditions for tree growth can be deduced from a published extreme scenario, which envisions large-scale afforestation of deserts (Ornstein et al., 2009).
It seems advisable to combine proposed NET methods to achieve an optimal carbon pool management for negative emissions and ensure food security over centuries at the global scale. To achieve this, interdisciplinary efforts are necessary (Fig. 1) and some of the key issues are reviewed here to point out the future research directions.
Increasing atmospheric CO2 concentrations and an increasing world population will lead to challenges in the nutritional supply for large parts of Earth's population (Smith and Myers, 2018; Myers et al., 2014). In combination with partly declining resources of natural mineral fertilizers (Manning, 2015, and Sect. S1 in the Supplement), alternative nutrient supplies, i.e., from rock products, are of high interest (Ciceri and Allanore, 2019). This idea has been discussed earlier (van Straaten, 2006, 2002) and was recently revived in the context of EW (Beerling et al., 2018; Hartmann et al., 2013). However, this issue extends further, if biomass-based NETs are considered for large-scale deployment. While nutrients like P or K are normally supplied via mineral dissolution in natural systems, nitrogen is in general supplied via fixation of N from the atmosphere (Graham and Vance, 2000). In some ecosystems N supply via rocks might be a relevant source (Houlton et al., 2018; Holloway and Dahlgren, 2002). In general, and specifically under intensified demand scenarios created by enhanced biomass growth rock, rock N supply will not keep up with the demand.
Many options of carbon dioxide removal rely on the production of biomass (i.e., biochar, afforestation, carbon capture and storage from bioenergy (BECCS), biofuels). These carbon dioxide removal (CDR) methods demand, if driven to an optimum, more geogenic nutrients than typically available to plants from the soil–rock systems in the long term, specifically in humid, tropical areas, where soils are deeply weathered and show naturally low nutrient contents (Hamdan and Bumham, 1996) that could not supply an additional intense biomass growth. A study on commercially exploited forests in the US points out that intensive harvest can withdraw more nutrients from the soils than can naturally be resupplied (de Oliveira Garcia et al., 2018).
The intensive withdrawal of nutrients should be included in a framework for biogeochemical cycle management under NET deployment. The withdrawal of K and P from cropland amounts globally to more than 8 Mt a−1 each (Fig. S2-2). For many ecosystems the natural resupply and potentially limiting effects under absence of deliberate fertilization practices are unknown or merely based on meta-analyses or model studies.
Due to desired global carbon sequestration goals (as in models for afforestation), growth rates will likely be driven to the maximum, which implies an increased demand of nutrients. Models show that N and P limit the global carbon sequestration potential for forests (Goll et al., 2012; Kracher, 2017). Nutrient release by EW can therefore play a relevant role in supporting the high demand. Particular rock classes contain, on average, higher K, P (Fig. 3), or micronutrients like Zn or Se, than others. To ensure a balanced supply of the needed elements, it is therefore necessary to consider more than one specific rock type during EW application.
Considering a subtropical weathering scenario in combination with Miscanthus growth for BECCS, acid igneous rocks show a high potential to (partly) resupply extracted potassium, while (ultra-)basic rocks can (partly) resupply phosphorus (Fig. 3). Many earlier studies on EW focussed on dunite to maximize inorganic CO2 sequestration, with the side effect of adding high levels of Ni and Cr to the system (e.g., Schuiling and Krijgsman, 2006; Hangx and Spiers, 2009). Later, basalt was added to the discussion (Beerling et al., 2018; Strefler et al., 2018; Hartmann et al., 2013). It is characterized by an elevated geogenic nutrient supply compared to ultrabasic rocks like dunite (Fig. 3), but still features a sufficiently high inorganic CO2 sequestration potential (Fig. 2, and Strefler et al., 2018). Future application scenarios will likely use a mixture of locally available material to optimize both organic and inorganic carbon storage. Optimizing the nutrient composition may come at the price of reducing the inorganic carbon sequestration potential, as some rock types with high nutrient content have low sequestration potentials (Fig. 2). If additional soil properties, like cation exchange capacity, water content/hydrology, and pH, are optimized, this reduction of inorganic carbon sequestration may be compensated for by elevated biomass uptake and organic carbon storage.
The introduction of additional nutrients to the soil system will not necessarily lead to an additional CO2 uptake and increased CO2 sequestration potentials of biomass-based NETs, if enough nutrients are supplied by traditional fertilization. However, forest areas may benefit from slow-release nutrients available long term as they may be less easy to resupply on a regular basis by agrotechnical machinery. Also, industrial fertilizer may be unaffordable in low-income regions; thus rock products could replace parts of the fertilizer (Ciceri and Allanore, 2019). A wider adoption of rock product utilization may also lead to the development of new and optimized application techniques.
Nutrients released from industrial fertilizers or from natural rock products can be taken up by the plant, washed away, or retained by the properties of the soil. The latter is called retention capacity and is important to store nutrients in a plant-available form. It has been shown that the weathering of basaltic material increases the cation exchange capacity, leading to an increased retention of nutrients (Anda et al., 2013, 2015). This is especially important for areas in which nutrients from industrial fertilizer material are quickly washed out, e.g., from the deeply weathered soils (e.g., Oxisols) in tropical regions (Leonardos et al., 1987; Ciceri et al., 2017). In such settings, it will be favorable to establish improved soil conditions with optimized nutrient retention.
Another application case is the fertilization of forests, specifically in areas which are reforested after agricultural use. With increasing atmospheric CO2 concentrations, an increase in biomass productivity in nonagricultural areas is expected through the CO2 fertilization effect (e.g., Ciais et al., 1995; Körner et al., 2007; Norby and Zak, 2011), especially with regard to afforestation efforts and general tree growth. This effect has yet to be clearly shown (Leuzinger et al., 2011), and is likely limited by soil fertility (Oren et al., 2001; Bader et al., 2013). It can already be observed that nutrient supply by rock weathering, specifically P, K, Mg, and Ca, can be the limiting factor of tree growth under elevated atmospheric CO2 (Jonard et al., 2015). Woodland soils might be amended with selected minerals or rocks to supply sufficient nutrients to keep up growth under elevated atmospheric pCO2 conditions and organically bind carbon, a scenario that should be explored further for its potential to enlarge affected carbon pools. At some point, depending on the environmental setting, biomass growth will be limited by nutrient supply and as such, model outputs for CO2 sequestration potentials of afforestation are likely to be overestimated, if geogenic nutrient cycles are not included in the assessment, as Goll et al. (2012) have shown, for example, for the C, N, and P cycles using a model.
The CO2 sequestration effect of afforestation is even larger if soil organic carbon changes are taken into consideration: depending on the underlying lithology, the organic carbon pools can be increased (Li et al., 2017), a process that may be optimized by the spreading of selected rock products.
Overall, specific element deficits in soils need to be mapped, since they can also affect the plant content of valuable, if not essential, elements for human nutrition (Zhang et al., 2017; Hengl et al., 2017; White and Zasoski, 1999). It is necessary to be able to predict which application amounts of elements causes a certain response in the biomass pool above and below ground. Such data are still scarce and inconclusive (Manning, 2010) but are needed if EW should be used as a method to help manage carbon and nutrient pools.
Biochar is another NET that has a beneficial effect on the retention of nutrients (Fig. 1). Due to its large surface area and increased cation exchange capacity, nutrients can be sustainably retained in soils (Lehmann, 2007; Liang et al., 2006), effectively saving applied fertilizer (Laird et al., 2010).
Increased nutrient retention may increase the overall CO2 sequestration potential of biomass-based NETs through the long-term availability of nutrients. However, the order of magnitude of the effect remains to be shown.
The availability of water is essential for high crop yields (Rockstrom et al., 2007), and soil hydraulic properties fundamentally steer the availability of water to plants (Bodner et al., 2015; Pinheiro et al., 2019). The soil hydraulic conductivity is a measure of how easily water can percolate though the soil column. It depends largely on the grain size distribution of the soil. Roughly, coarse (sandy) soils have a higher hydraulic conductivity than fine (clayey) soils (Rawls et al., 1982). Spreading large amounts of rock products with very small grain sizes (silty to clayey) on land potentially leads to a decrease in soil hydraulic conductivity, which may lead to decreased weathering speeds due to local pore water oversaturation or enhanced surface runoff. However, there are some indications that the addition of biochar can be used to control hydraulic conductivity (Masiello et al., 2015; Barnes et al., 2014), which could enable the use of smaller grain sizes for EW, enhancing its potential, which strongly depends on the grain size (Strefler et al., 2018).
As another hydraulic property, the water holding capacity determines how much water is kept in the soils and potentially is available to plants. This parameter becomes increasingly important with more frequently appearing droughts due to climate change (Kang et al., 2009). Biochar could be used to improve the water holding capacities of soils (Omondi et al., 2016; Liu et al., 2017), and also increase the plant available water in some cases (Masiello et al., 2015). This may render dryer regions or areas with unfavorable soil physical properties (Basso et al., 2013) usable for bioenergy plants and/or afforestation. There are also indications that improvement of soil hydrology by biochar may increase yield potentials (Akhtar et al., 2014; Xu et al., 2015; Al-Wabel et al., 2018).
It is important to point out that all potential changes in soil physical properties due to biochar application strongly depend on its type, more specifically the feedstock and production temperature (Gul et al., 2015). The combination of rock product and biochar application, however, was not addressed in previous research at all but may provide relevant potential to increase and maintain soil carbon.
Soil pH steers the availability of elements to plants (Kabata-Pendias, 2010; Loomis and Morris, 1983). At pH values well below 7, nutrients become less available to plants and potentially harmful trace metals are successively mobilized. Nitrogen-fixing bacteria are also depending on a specific pH (Graham and Vance, 2000). Soil acidification on heavily used cropland is a problem (Helyar and Porter, 1989), which may lead to a decrease in crop yields. The main reason is the higher mobility of most exchangeable metals at low pH, which decreases logarithmically with increasing pH (Kabata-Pendias, 2010; Robinson et al., 1996; Tack et al., 1996; Harter, 1983). Levels of pH 6 and higher generally ensure very low levels of exchangeable harmful metals, with the exception of arsenic, depending on the oxidation state (Dixit and Hering, 2003). The release of base cations from rock flour leads to a soil pH increase. Studies have demonstrated the effectiveness of basalt powder application in raising the soil pH up to 8 and higher (e.g., Gillman et al., 2001; Nunes et al., 2014). The effect is similar to agricultural liming, which is a common practice to counteract soil acidification on cropland (West and McBride, 2005). Despite the fast dissolution rate of carbonate minerals, they have in general, until today, not been considered for EW scenarios, because of possible carbonate precipitation and subsequent CO2 release in the ocean (Hartmann et al., 2013) or due to the potential release of CO2 by excess fertilizer application (Semhi et al., 2000; Perrin et al., 2008). The potential of carbonates in EW strategies remains to be studied, while silicate application is the focus of recent research (Taylor et al., 2015). It could be a potential economic benefit to replace agricultural lime with silicate rock flour, bearing in mind that silicate dissolution rates are in general several orders of magnitude lower, with strong variability between different minerals (Lasaga, 1995; Brantley et al., 2008). Thus, the efficacy is decreased due to the slower release rate of cations, but other properties like nutrient retention or soil hydrology might be improved (see Sect. 4). It remains to be investigated how (fast) the termination of pH-stabilizing silicate rock powder application will affect the soils. If relatively immobile potentially harmful metals accumulate at elevated pH values over the application period, an excessive and harmful release of toxic substances might occur in case of a future drop of pH due to changes in pH-controlling minerals, land use, or general environmental conditions. Once the deployment of material rich in trace elements of concern is started, it is obligatory to maintain a stabilized pH environment, strengthening the need for material with low harmful trace element concentrations (requirements may differ depending on ecosystem type).
Assuming that pH stabilization and beneficial changes in soil hydrology (see previous section) are achievable with biochar and EW, a significant additional CO2 uptake can be expected, based on the fact that soils that could not support sustainable biomass growth before are made usable for biomass-based NETs.
Chemical weathering of rocks can be significantly mediated by macro- and microbiota (Schwartzman and Volk, 1989; Uroz et al., 2009; Hoffland et al., 2004; Blouin et al., 2013), although the order of magnitude is a matter of debate (Drever, 1994). This is specifically the case for mycorrhizal fungi and microbes, which create physicochemical conditions that accelerate the dissolution of minerals (Taylor et al., 2015). The weatherability of minerals depends on the type of bioinoculant (Nishanth and Biswas, 2008; Benzerara et al., 2005; Cuadros, 2018), implicating that a supervision and management of the soil microbiota is necessary to optimize both crop yields and rock weathering. Microbial populations in soils respond to the addition of biochar (Warnock et al., 2007) by providing a refuge for bacteria and fungi (Pietikainen et al., 2000; Saito, 1990), increasing nutrient availability, creating favorable pH conditions, and other processes discussed in Lehmann et al. (2011).
Earthworms have been observed to thrive in biochar-amended soils (Topoliantz and Ponge, 2005). Increased abundance of earthworms will likely increase bioturbation effects (Carcaillet, 2001; Major et al., 2010), leading to a better distribution of biochar and rock flour in deeper layers of the amended soils, increasing reactive surfaces of mineral grains. Bioturbation might also be a key process to achieve high CO2 sequestration rates by weathering, as earthworms can enhance mineral weathering (Carpenter et al., 2007, 2008) and contribute to the downward transport of added rock products into deeper soil layers (Taylor et al., 2015).
Soils are an important sink in the environmental cycling of trace metals (Kabata-Pendias, 1993). In addition to naturally occurring concentrations, depending on the underlying lithology, the major source of trace metals to soils is agricultural practice, leading to an enrichment due to the application of manure, sewage sludge, fertilizers, and pesticides, which all contain metals to a certain extent (Gonnelli and Renella, 2013). Field studies using sewage sludge as fertilizer have shown a marked uptake by the crops and increased mobilization of trace metals in the runoff water (Alloway, 2013). Adding to the anthropogenic input, the introduction of additional rock products with elevated levels of trace metals (Fig. 4) could lead to a critical exceedance of environmental thresholds if improper rock material is used due to inconsiderate management. This, however, relates to the solubility of minerals within the used rock type and the redox and pH conditions. An EW soil incubation experiment using an olivine-rich rock product, with elevated Ni and Cr concentrations in the source material (Fig. 4), showed only a few occurrences of elevated Cr levels but no Ni increase in the aquatic solution compared to a blank treatment, leading to the conclusion that the soil solid phase will be successively enriched in those elements (Renforth et al., 2015).
The availability of heavy metals to biota remains an issue of ongoing discussion (Nagajyoti et al., 2010). The main elements of concern in source rocks with the highest sequestration potential (ultramafic rocks) are Ni and Cr. In particular the earlier discussed dunite application for EW must trigger discussion about its high Cr and Ni contents (Fig. 4) and is therefore ruled out for large-scale application on cropland.
If an application with rocks of high trace metal concentrations of concern is considered, it is necessary to stabilize the soil pH even after cessation of such actions in order to maintain the fixation of toxic elements because of the strong pH control on metal mobility. A study of long-term sewage sludge application has shown that the pH had to be stabilized by liming in order to prevent phytotoxicity of Cu and Zn (McBride et al., 2004). Additionally, the metal availability to plants has been shown to be influenced by the soil texture, with marked differences for different elements (Qian et al., 1996). This underlines the necessity to control or specifically design the grain size distribution of the soil to control water content, pH, and oxygen content. To further ameliorate the issue, biochar, which has been shown to immobilize heavy metals in soils, depending on feedstock and production conditions (Ahmad et al., 2014; Beesley et al., 2011), could be jointly applied with rock powder. This would mean that potential limitations of fertilizer or rock spreading due to thresholds put in place for environmental protection could be overcome by a sensible management of biochar utilization. Applying biochar products does not remove elements of concern, but the problem of heavy metal accumulation could be dampened by bioremediation through heavy-metal-accumulating plants (Rajkumar et al., 2012). This in turn could be a potential new source of raw material for industrial use (Schuiling, 2013), though it is likely not applicable on a global scale since this would compete against food and energy plant production, which is already an issue (Tilman et al., 2009).
The alleviation of trace metal effects does not directly affect CO2 sequestration rates but could overall increase potential deployment areas for EW.
Looking forward it is likely that a portfolio of options will be established to optimize the sequestration effect and minimize negative impacts. The combination of previously separately studied NETs to increase the sequestered carbon pool should consider the management of biogeochemical cycles and optimize the combined application of Enhanced Weathering and biochar in the context of biomass-based methods like BECCS and afforestation to maximize carbon capture as well as food production. It is therefore essential to address combined effects of NET co-deployment in future research projects.
As all presented interactions take place in the soil, future research should put a focus on creating an optimized soil product for optimal long-term sustainable carbon management. We propose that research around biomass-based NET interactions becomes the science of artificial soil products, which are most likely created on depleted and degraded soils, especially in the (sub)tropics. It may consist of the locally available “base soil” mixed with biochar products to enhance hydraulic properties and nutrient retention, as well as rock powder, which raises the soil pH, provides nutrients, and sequesters CO2 at the same time. This engineered and managed soil could increase carbon pools and crop production, while contributing to tackle the issue of climate change. It remains to be studied where suitable material is available at the regional scale (Sect. S5). The parameterization of element release rates permitting a sustainable management is still subject to large uncertainties and the effects of massive rock product spreading will change the soil structure to an extent that remains to be explored.
The introduction of non-authigenic material into the environment, even if of bio- or geogenic origin, will increase the entropy of the system, making it difficult and expensive (from the viewpoint of energy and economics) to quickly revert back into the “undisturbed” state once large-scale deployment has started. Thus, the continuous deployment of NETs at the global scale at an order of magnitude that would measurably impact atmospheric CO2 levels must be seriously weighed. However, the high probability of NET adoption in the near future makes it imperative to create efficient cooperation networks across all involved disciplines in order to conceive the necessary knowledge on actual CO2 sequestration potentials and century-scale global carbon pool changes.
No unique data were created. All dataset sources used were referenced. All resulting data, underlying the figures, are provided in the Supplement.
The supplement related to this article is available online at: https://doi.org/10.5194/bg-16-2949-2019-supplement.
This article was conceived by the joint work of JH and TA. Both participated in discussions, planning, and writing, with the lead of TA.
The authors declare that they have no conflict of interest.
This research was executed with the financial support of the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) priority program on “Climate Engineering–Risks, Challenges and Opportunities?” and specifically the CEMICS2 project. Further support came from the DFG under Germany's Excellence Strategy – EXC 2037 “Climate, Climatic Change, and Society” – project number 390683824, contribution to the Center for Earth System Research and Sustainability (CEN) of Universität Hamburg. We are grateful for the constructive comments and suggestions from the reviewers and editor.
This research has been supported by the Deutsche Forschungsgemeinschaft (DFG grant nos. SPP1689, EXC177, and EXC2037).
This paper was edited by Anja Rammig and reviewed by two anonymous referees.
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