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Review

Impacts of Permafrost Degradation on Carbon Stocks and Emissions under a Warming Climate: A Review

1
School of Civil Engineering, Institute of Cold-Regions Science and Engineering, Northeast-China Observatory and Research-Station of Permafrost Geo-Environment (Ministry of Education), Northeast Forestry University, Harbin 150040, China
2
State Key Laboratory of Frozen Soils Engineering, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China
3
School of Hydraulic Engineering and Electric Power, Heilongjiang University, Harbin 150040, China
*
Authors to whom correspondence should be addressed.
Atmosphere 2021, 12(11), 1425; https://doi.org/10.3390/atmos12111425
Submission received: 18 September 2021 / Revised: 25 October 2021 / Accepted: 26 October 2021 / Published: 29 October 2021
(This article belongs to the Special Issue Climate Change and Its Effects on Permafrost)

Abstract

:
A huge amount of carbon (C) is stored in permafrost regions. Climate warming and permafrost degradation induce gradual and abrupt carbon emissions into both the atmosphere and hydrosphere. In this paper, we review and synthesize recent advances in studies on carbon stocks in permafrost regions, biodegradability of permafrost organic carbon (POC), carbon emissions, and modeling/projecting permafrost carbon feedback to climate warming. The results showed that: (1) A large amount of organic carbon (1460–1600 PgC) is stored in permafrost regions, while there are large uncertainties in the estimation of carbon pools in subsea permafrost and in clathrates in terrestrial permafrost regions and offshore clathrate reservoirs; (2) many studies indicate that carbon pools in Circum-Arctic regions are on the rise despite the increasing release of POC under a warming climate, because of enhancing carbon uptake of boreal and arctic ecosystems; however, some ecosystem model studies indicate otherwise, that the permafrost carbon pool tends to decline as a result of conversion of permafrost regions from atmospheric sink to source under a warming climate; (3) multiple environmental factors affect the decomposability of POC, including ground hydrothermal regimes, carbon/nitrogen (C/N) ratio, organic carbon contents, and microbial communities, among others; and (4) however, results from modeling and projecting studies on the feedbacks of POC to climate warming indicate no conclusive or substantial acceleration of climate warming from POC emission and permafrost degradation over the 21st century. These projections may potentially underestimate the POC feedbacks to climate warming if abrupt POC emissions are not taken into account. We advise that studies on permafrost carbon feedbacks to climate warming should also focus more on the carbon feedbacks from the rapid permafrost degradation, such as thermokarst processes, gas hydrate destabilization, and wildfire-induced permafrost degradation. More attention should be paid to carbon emissions from aquatic systems because of their roles in channeling POC release and their significant methane release potentials.

1. Introduction

A large quantity of carbon (C) (1460–1600 Pg C) is stored in permafrost regions in the northern hemisphere [1,2]. Permafrost organic carbon (POC) amounts to nearly twice the size of the carbon pool in the atmosphere (~730 Pg C), or about thrice that of terrestrial vegetation C [3,4]. Clathrates in terrestrial and subsea permafrost are also included in this permafrost C inventory. Carbon stocks in permafrost regions are a globally important C pool in climate-sensitive cold regions, such as the arctic, boreal, alpine, and high-plateau regions [5]. In recent decades, persistent climatic warming at an average rate of 0.060 °C·yr−1 has been extensively reported in high-latitudinal regions, which is twice faster than that of the global average [6]. On the Qinghai-Tibet Plateau (QTP), the largest expanse of elevational permafrost on Earth, the average rate of climate warming was at 0.045 °C·yr−1 (1980–2018) [7].
Climate warming will unlock organic carbon and nitrogen sequestered in permafrost, emitting large quantities of greenhouse gases, such as CO2, CH4, and N2O, by microbial decomposition, into the atmosphere, and forming positive feedback to climate warming [2,3,8]. Currently, carbon fluxes in Arctic permafrost regions are estimated as a CO2 sink at rates of 0.3–0.6 Pg C·yr−1 and a CH4 source at rates of 23–75 Tg C·yr−1 and they are projected to be both CO2 and strengthened CH4 sources by 2100 [9]. Another portion of POC will be delivered into the aquatic ecosystems in forms of particulate organic C (PTOC) and dissolved organic C (DOC) (e.g., [10,11,12]). Released POC will go into fluvial systems and eventually be deposited into deep oceans, altering the terrestrial–oceanic C distribution. Organic C in aquatic systems can also be further microbially converted into CO2 or CH4 [13,14,15].
Configurations of permafrost degradation can be characterized by gradual degradation or abrupt permafrost thaw [16]. The former, such as the top-down degradation, shrinkage of permafrost extent, and others, will induce relatively slow, yet extensive C emissions from permafrost regions [2]. By pooling observations from more than 100 Arctic field sites, Natali et al. (2019) estimated an average release of 1662 Tg C (2003–2017) from permafrost each winter, double that of past estimates [17]. However, abrupt permafrost degradation will induce imminent C release to both the atmosphere and aquatic systems. A mega-slump in Bataigaika, upper Yana River Basin, Eastern Siberia, may have emitted millions of tons of CH4 into the atmosphere over a very short time [18]. Arctic coastal lowlands consist of organic- and ice-rich permafrost and are endowed with a significant DOC storage [19]. Tanski et al. (2019) pointed out that the erosion and recession of these coasts could release a large amount of permafrost carbon directly into the Arctic Ocean [14].
Carbon emission in responding to permafrost degradation is impacted by a synergy of multiple environmental factors (e.g., [3,8,20,21,22]). Mutual interactions between these environmental factors and microbial activities in the soil are complex [23]. Without an adequate understanding of the mechanisms of microbial activities in responding to (cryo-) pedogenesis, it is difficult to accurately model, simulate, and predict C emission under scenarios of permafrost thawing [24]. Thus, in this paper, we review and synthesize recent studies on and research advances in C stock and its stability in permafrost regions, biodegradability of organic C in permafrost regions, C emission impacted by permafrost degradation, and model projecting/modeling of permafrost C feedback to climate warming. This study can help provide a baseline understanding on POC stock and its positive feedbacks to climate warming and close the research gaps on permafrost C dynamics.

2. Carbon Stocks in Permafrost Regions

2.1. Soil Organic Carbon (SOC) Stocks in Permafrost Regions

Soil is the largest organic C pool in terrestrial ecosystems. It is also the most important terrestrial organic C pool in permafrost regions. Stocks of soil organic carbon (SOC) in permafrost regions have been intensively studied in recent years (e.g., [1,25,26,27,28,29,30,31,32,33,34,35]). With different estimation methods or models, associated soil depths or horizons, recent geological time, and ecosystem types, SOC stocks have been estimated in different permafrost regions. Parts of these estimations are listed in Table 1.
In the circumpolar permafrost regions (17.8 × 106 km2), 15% of global land area, SOC storage at depths of 0–3 m is estimated at 1035 ± 150 Pg C, equal to nearly one-third of global SOC storage at the same depths of 0–3 m [2]. Nearly half of this SOC is stored at depths of 0–1 m in permafrost regions (472 ± 27 Pg C), and SOC density declines downwards [11,34]. About 58–371 Pg C is found in the ice- and organic-rich and thick yedoma permafrost (at depths of 0–20 m) with an area extent less than 1.4 × 106 km2 [27]. In the High Arctic of 1.1 × 106 km2 in areal extent and comparable to that of yedoma regions, SOC is estimated at 34 ± 16 Pg C (0–3 m in depth). The Antarctica is extensively covered with ice and with only a 0.35% ice-free area (49,500 km2). An SOC of 0.725 Pg C is estimated for Antarctic soils [30]. Spatial distribution of SOC in latitudinal permafrost regions indicates huge surface organic C stocks (<1 m) and yedoma permafrost C at depth and boreal/subarctic peatlands with the highest C density (59.1–97.2 kg∙m−3) among permafrost regions; this may potentially act as future C sources for the atmosphere and aquatic systems. Since the Last Glacial Maximum (LGM at 30–20 ka B. P.), permafrost areal extents have declined substantially from the LGM to present, while the total SOC has increased by ~300 Pg C, with limited peatlands (0.87 × 106 km2) having been developed, forming a major atmospheric C sink and sequestrating 427–653 Pg C from the atmosphere [31]. The SOC in yedoma permafrost regions during the LGM is estimated at 390–446 Pg C (>3 m in depth), in comparison with that of the present at 58–371 Pg C [27,28]. They may suggest a substantial carbon transfer (ca. 75–332 Pg C) from the pedosphere and cryosphere to the atmosphere and hydrosphere. Therefore, permafrost C has not been a net C source since the LGM, but an internal C transfer has occurred within northern permafrost C pools [31].
Elevational permafrost covers an area of 2.5 × 106–4.9 × 106 km2 [43]. The areal extent of the QTP (ca. 2.6 × 106 km2), about one-half of which is underlain by alpine and high-plateau permafrost, accounts for nearly 70% of the areal extent of elevational permafrost in the world [44,45,46,47]. The SOC stock at depths of 0–3 m in plateau permafrost regions is estimated at 21.69–42.7 Pg C [34,37,38]. On the QTP and in other alpine/high-plateau permafrost regions, SOC content is generally low, with an average of 15.2 ± 1.3 kg m−2, due to thin, sedimentary, or overburdened strata and poorly developed soil [43].

2.2. Subsea Permafrost Carbon Storage

During the LGM, the global sea level was ~125 m (120–150 m) lower than that of the present [48]. The continental shelf of the Arctic Ocean, especially in Eastern Siberia and Alaska, is among the globally shallowest continental shelves, with an area extent of ~3.0 × 106 km2 [2]. Under intermittent warming climates since the Late Pleistocene to the early Holocene, the rising of sea levels has resulted in frequently inundated arctic tundra ecosystems in the coastal terrains. In the Last Interglacial Stage (127–116 ka BP), global sea level was 9–11 m higher than that of the present [48]. As a result of submerging extensive LGM permafrost, a large stock of carbon is stored in the subsea permafrost domains. Sayedi et al. (2020) reported an organic carbon pool of 560 Pg C (170–740, 90% confidence level) in subsea permafrost and of 45 Pg C (10–110) as methane hydrates [49]. The subsea permafrost has undergone degradation, transferring POC into both the atmosphere and the Arctic Ocean by coastal erosion [2]. An annual CO2 emission of ~29 Tg C from the subsea permafrost in Arctic Siberia (9.87 × 105 km2) [50] and 38 Tg C (13–110) from the subsea permafrost has been estimated. Annual CH4 emission ranges from 3–18 Tg C from the subsea permafrost [49,51,52]. Insufficient measurements of subsea permafrost largely increase uncertainties of estimates in subsea carbon storage and a wide range of carbon emission rates. Current assessments of C emission from subsea permafrost are more focused on atmospheric C emission, and they largely neglect the lateral C emission as dissolved/particulate organic carbon (DOC/PTOC) into the Arctic waters, which may underestimate the magnitude of subsea permafrost domains as a carbon source.

2.3. Methane Hydrate Storages in Permafrost Regions

Methane hydrates in permafrost regions have high potentials of CH4 emission due to the warming climate and greater unit warming power of CH4 in the atmosphere in comparison with that of CO2 [53]. An early estimation of CH4 hydrates in the Arctic permafrost regions was reported as 580 Pg C [54]. Later, a more conservative estimation yielded a stock of 20 Pg C sequestered in Arctic permafrost regions [55]. Methane hydrates in subsea permafrost domains are 45 Pg C [49]. Methane hydrates on the QTP amount to 175.4 ± 39.2 Pg C [56]. However, this estimate awaits further confirmation and is highly uncertain. Methane hydrates in permafrost regions are mostly present in coastal areas in the Circum-Arctic regions [57]. Due to the high vulnerability to external alterations of temperature and pressure for the stabilization zone of methane hydrates [58], climate warming and natural disasters, such as volcanic abruption, submarine earthquake, subsea landslides, and large tsunami, can possibly destabilize methane hydrates and result in abrupt C emissions.
The carbon emission of destabilizing methane hydrates has been started [2]. Kretschmer et al. (2015) predicted an 0.03% loss of global inventory of methane hydrates (473 Tg C) in the coming 100 years by melting hydrates [59]. Ruppel and Kessler (2017) emphasized that the large burial depth and high density of overlying materials of methane hydrates will relieve and retard the responses of methane hydrates to the warming climate [58]. Jin and Cheng (1997) noted that the CH4 emission from melting methane hydrates will not cause a significant impact on the global climate by 2100 [57]. However, Maslin et al. (2010) suggested disastrous positive feedbacks by abrupt CH4 emissions from destabilizing methane hydrates [53]. As shown in Figure 1d, the explosion of permafrost mounds on the Yamal Peninsula possibly has abruptly released a large amount of methane carbon into the atmosphere, and more than 400 sealed craters was recently found and reported from more than 7000 Arctic permafrost mounds [60].

3. Biodegradability of Permafrost Organic Carbon (POC)

The biodegradability of POC determines the responsiveness and intensity of the feedback of permafrost C stocks to climate warming. Both field observations and laboratory incubation have indicated a high biodegradability of POC. By pooling the incubation data sets from 121 observation sites and 23 ecosystems, Schädel et al. (2014) concluded that 20–90% of POC could be potentially mineralized within 50 incubation years [61]. Plaza et al. (2019) reported on the post-degradation organic C content in permafrost soils and found an annual rate of carbon loss as high as 4.5% yr−1 [22]. In peatlands permafrost regions in Western Canada, newly thawed permafrost can result in a carbon loss rate ranging from 0.2% to 25% by 2100 [62].
Biodegradability of POC is determined by the properties of permafrost C, per se, as well as environmental factors, such as the microbial community (e.g., microbe abundance, community structure, and microbial types), SOC compositions, soil C/N ratio, soil hydrothermal conditions, and Eh and pH, among others [61,63,64,65]. The incubation experiment is widely adopted to examine the mechanisms of POC biodegradation [61,63,66]. Mackelprang et al. (2011) analyzed impacts of permafrost thaw on functional genes and CH4 emission in incubation experiments, highlighting a rapid shift in functional genes and methanogenesis from frozen to thawed permafrost soils [67]. Xue et al. (2016) conducted an 1.5-year field warming condition/treatment and found markedly increased microbial richness and ecosystem respiration (38%) in a tundra ecosystem underlain by permafrost [68]. Kwon et al. (2019) noted that the microbial community composition would be changed, and species richness were closely related to subsequent C emissions upon thawing of permafrost [69]. Soil C/N ratio is also an important controller of POC [61,65]. Assembling and analysis of the data of aerobic soil incubations from 23 ecosystems in northern permafrost regions, it was evident that the slow cycling pool size was closely related with the soil C/N ratios, an index for upscaling biodegradability of POC across the northern permafrost regions [61]. Ecosystem types and terrestrial vegetation biomes also influence the biodegradability of SOC and POC in permafrost regions by impacting compositions of SOC, increased alkyl C, and decreased recalcitrant aromatic C (lignin-derived) compounds [65,70,71]. After classifying the biodegradability of SOC in permafrost regions according to landscape classes and soil geochemical parameters (e.g., C/N ratio and SOC content), Kuhry et al. (2020) also upscaled the potential greenhouse gas release from POC [65]. Soil hydrothermal conditions can also determine the decomposability and forms of C emissions due to the aerobic or anaerobic environments [2,63,72]. Treat et al. (2015) collected the results from incubation experiments all over the northern permafrost regions and compared the results from different landscapes (vegetation types), soil properties (e.g., pH and soil types), and environmental factors (e.g., water table and temperature) to project the biodegradability of SOC emitted as methane [73].
Current data sets on incubation experiments are essential to quantify the biodegradability of POC across the northern permafrost regions. With a more comprehensive environmental factor data set of laboratory incubations for upscaling potential greenhouse gas release from POC, in addition to the processive knowledge of mechanisms of potential greenhouse gas release from POC, C emission can be projected more accurately under uncertain future environmental conditions.

4. Carbon Emissions in Regions of Degrading Permafrost

4.1. Atmospheric CH4 and CO2 Emission Induced by Permafrost Degradation

Permafrost degradation can be manifested by a gradual mode, such as deepening active layer, shrinking areal extent of permafrost, and gradually thinning permafrost, and/or in an abrupt manner, such as the development of thermokarst, retrogressive thaw slumping, frozen debris flows, landslides due to active-layer detachment failures, and coastal thermal erosion, landslides, and collapses.
Atmospheric CH4 and CO2 emissions have been studied in permafrost regions in the arctic, subarctic, and boreal regions and on the QTP, with varied ecozones, including tundra, taiga forest, wetlands, peatlands, meadows, and steppes undergoing gradual permafrost degradation (e.g., [22,74,75,76]. In the arctic tundra ecosystem, based on the projected climate warming, Hollesen et al. (2011) reported a rate of CO2 emission at ~40 g C m−2 yr−1 at present and at 120–213 g C m−2 yr−1 in the future. In low boreal wetlands [77], Roulet et al. (1992) reported CH4 emission rates up to 5.7 g C m−2 yr−1 in beaver ponds and 3.6 g C m−2 yr−1 in thicket swamps [74]. In boreal taiga permafrost regions, the average rate of CO2 emission was estimated at 19 g C m−2 yr−1 [78]. In permafrost regions on the QTP, an early report on the amount (rate) of CH4 emission from the cold wetlands on the QTP was estimated at 0.7–0.9 Tg C·yr−1 (5.3–6.8 g C m−2 yr−1) [75]. This estimation was later updated as 0.215–0.412 Tg C·yr−1 (2.4–4.5 g C m−2 yr−1) based on more extensive and sophisticated studies [79]. Tao et al. (2007) reported rates of CO2 emission at 191.23 g C m−2 yr−1 for alpine meadows in permafrost regions on the northeastern QTP [80].
An inconsistent regional estimation of carbon sink and/or source potentials under a warming climate has been reported for regions of degrading permafrost with varied ecosystem types. Virkkala et al. (2021) estimated the boreal regions as a carbon sink based on a net ecosystem exchange (NEE) of −46 g C m−2 yr−1, because of the photosynthetic offset of the released CO2 (soil respiration) [81] and the Arctic tundra served as a carbon source at 10 g C m−2 yr−1 [82]. In the High-Arctic semi-desert regions, the carbon sink could strengthen by an order of magnitude under a warmer-wetter climate, but the summer carbon sink could be reduced by 55% under just a warming treatment [83]. In arctic peatlands permafrost regions, a low water table on peatlands under dry conditions had enhanced the POC feedback by adding atmospheric CO2 emissions. When the peatland water table remained low, Arctic peatlands would continue to serve as a potent C sink [84]. Alases are mature thermokarst landscape covering 17% central Yakutia lowland [85]. Alases ecosystem with forest landcover is a reported small CH4 sink (0.01–0.3 C m−2 yr−1), with wet-grass and ponded surface (1.7–86.4 g C m−2 yr−1) [85,86].
In contrast to gradual permafrost degradation, abrupt permafrost degradation, such as thermokarst lakes (Figure 1a), thermal erosion gullies (Figure 1b), giant sinkholes (Figure 1c), active layer detachment landslide offshore in the Arctic Canada (Figure 1d), and retrogressive thaw-slump (Figure 2), occurs in periods of days to several years. Walter et al. (2007) found CH4 bubbling from northern lakes at a rate of 0.06 ± 0.02 g CH4 m−2 d1 to the atmosphere [87]. In interior Alaska, methane emission from a thermokarst lake is reported at a rate of 0.15 ± 0.02 g CH4 m−2 d−1 [88]. CH4 emissions from thermokarst lakes from typical alas landscape are the reported highest rates in Arctic and subarctic regions [89]. Tanski et al. (2019) claimed that, when seawater eroded each gram of permafrost, 4.3 ± 1.0 mg CO2 would be released into the atmosphere [14]. Parker et al. (2021) simulated the abrupt thaw of excess ice and found excess-ice meltwater is effective in high CH4 emission; once ice melt is connected to a subsurface flow, CH4 efflux is limited [90]. With an areal extent of 3.6 × 106 km2, Circum-Arctic thermokarst landscapes cover about 20% of the northern permafrost region, with a similar POC feedback comparable to the extensive and overall permafrost degradation in a gradual manner [91,92]. Increased wildfire frequency and scales also contribute to abrupt carbon emission [6,93]. In 2020, an ever highest temperature (38 °C) was recorded in the Arctic and 35% more CO2 was released by wildfires in comparison with that in 2019 and earlier recorded since 2003 [94].

4.2. Lateral Carbon Flux in Regions of Degrading Permafrost

Under a warming climate, the lateral carbon flux, mainly in the form of dissolved organic carbon (DOC), particulate organic C (PTOC), and dissolved inorganic carbon (DIC), is also an important pathway of carbon emissions in regions of degrading permafrost [10,12,95,96,97,98].
After studying DOC concentrations in the rooting zone and groundwater in an Arctic taiga permafrost region, MacLean et al. (1999) reported a higher DOC in the rooting zone and a lower DOC in groundwater and springs [95]. This implies higher DOC fluxes in watersheds underlain by extensive permafrost in comparison with those by a limited presence of permafrost. This is probably due to the constrained water infiltration by permafrost. Walvoord and Striegl (2007) investigated changes in streamflow patterns in the Yukon River basin undergoing permafrost degradation and found a boosted groundwater contribution to streamflow (0.7–0.9% yr−1), but without a pervasive change in annual flow regimes and subsequently a decreased DOC flux and increased DIC flux [99]. Giesler et al. (2014) studied long-term (1982–2010) aquatic DOC and DIC exports from permafrost-dominated tundra catchments in northern Sweden and found a 9% increase in DIC and no clear trend in DOC [100]. Guo et al. (2015) studied permafrost in a wetland catchment in northeastern China and suggested an increased DOC export from the catchment due to the warming-wetting climate [101]. By integrating the riverine chemistry coupled with a decadal data set of discharge, Tank et al. (2016) reported increasing trends of DOC (+39.9%) and DIC (+12.5%) fluxes in the Mackenzie River basin [102].
PTOC is also a major form of organic C in rivers/streams in permafrost regions. McClelland et al. (2016) investigated PTOC flux from major Arctic rivers (e.g., Yenisey, Lena, Ob¢, Mackenzie, Yukon, and Kolyma) and found annual a PTOC export mainly concentrated in the spring (May and June) and winter PTOC export was less than 5% of annual fluxes [103]. Lamoureux and Lafrenière (2014) confirmed their results, noting most annual PTOC flux was exported in the snow-melting season and permafrost disturbances dominated summer PTOC flux [104]. Other research reported dominance of vegetation and fluvial erosion on fluvial PTOC (e.g., [105]). McClelland et al. (2016) presumed that topographical inclination and water velocity impacted fluvial PTOC export [103]. The change trends of lateral DOC, PTOC, and DIC fluxes in some individual northern or elevational permafrost regions were collected and sketched in Figure 3. Evidently, there were no consistent change trends of in-stream DOC, PTOC, or DIC fluxes in permafrost catchments.
Lateral C flux in regions of degrading permafrost is regulated and complicated by many geo-environmental factors (e.g., vegetation and snow cover, permafrost disturbances, hydrological pathways, and fluvial erosions). Discrepancy in estimates and/or predictions of changes in the permafrost environment in individual catchment and future climatic conditions lead to large uncertainties for changes in lateral C dynamics in permafrost regions. However, several recent studies have pointed out the significance of atmospheric C emission from aquatic systems, probably due to important conduits of POC and methane emission potentials (e.g., [15,113,114]). Under a warming climate, permafrost degradation will alter the lateral flux of organic C to aquatic systems. Thus, neglecting this lateral carbon flux will substantially underestimate the strength and channels of POC feedback to climate warming.

5. Modeling and Projecting Permafrost Carbon Feedback to Climate Warming

Permafrost C stocks, biodegradability, and emission of permafrost carbon are baselines of simulating permafrost C feedback to climate warming. Their studies can help make alerts for the risks of environmental changes and assure the economic and productive safety for policy makers [115,116,117,118,119,120,121,122,123,124,125,126,127,128,129].
Currently, studies on the model assessments of permafrost C feedback to climate warming include Earth system models or coupled assessment models, and simulations on abrupt degradation feedback for climate warming are starting to be paid more attention. Waelbroeck et al. (1997) coupled hydrological and thermal models with a net-CO2 flux model for simulating the C accumulation/emission in a tundra ecosystem [115]. Khvorostyanov et al. (2008) integrated a 1-D soil model with a permafrost model for investigating carbon flux from yedoma terrains [116]. Koven et al. (2011) employed the Organising Carbon and Hydrology In Dynamic Ecosystems (ORCHIDEE), a terrestrial ecosystem model coupled with methanogenesis processes, and simulated the potential of permafrost carbon feedback to climate warming [117]. MacDougall et al. (2012) adopted an oceanic and terrestrial carbon circulation model by coupling the freeze–thaw processes, including permafrost carbon, to assess the additional warming by permafrost degradation [118]. By coupling the Lund–Potsdam–Jena managed Land (LPJmL), a global vegetation model, and permafrost modules, Schaphoff et al. (2013) examined the carbon sink and/or source functions in northern permafrost regions [119]. Von Deimling et al. (2015) developed a multi-pool permafrost carbon model based on the observed permafrost carbon properties and by taking into account of the abrupt permafrost degradation, e.g., formation of thermokarst lakes and landslides [120]. Burke et al. (2017) integrated the Joint UK Land Environment Simulator (JULES) and the ORCHIDEE-MICT (aMeliorated Interactions between Carbon and Temperature) with the Integrated Model of Global Effects of climate aNomalies (IMOGEN) to compare with the simulation results with and without permafrost carbon and quantify the additional warming from permafrost carbon [121]. Walter et al. (2018) integrated the Community Land Model (CLM) with a physically based thermokarst lake model for simulating permafrost carbon emission by taking into account of abrupt-thaw carbon emissions [122]. Detailed information on some examples of models for evaluating the feedback of permafrost carbon to climate warming are listed in Table 2.
Models of permafrost carbon emission have evolved from simulations of hydrothermal processes integrated with terrestrial carbon cycle models to Earth system models for climate modeling. However, there are still large uncertainties in modeling and projection results. Considerations of simulating the thermokarsting processes largely constrain the feedback of real-time permafrost carbon release to climate systems, which is a major part of permafrost carbon transmitted to the atmosphere [92,122]. Moreover, fire-induced permafrost degradation may be another major source of permafrost C feedback to climate warming [72,124]. To date, this source from abrupt permafrost degradation is still missing from these carbon or ecosystem models.

6. Summary, Inadequacies, and Prospects

Estimations of permafrost C stocks have been intensively studied and data collection and computational procedures have been systematically and rapidly improving. There are still large uncertainties in estimating for the subsea permafrost C and gas hydrates in permafrost regions due to the scarce data in these regions. Emission rates of permafrost carbon in response to climate warming largely depend on the biodegradability of permafrost carbon. The practical biodegradability of POC is a synergy of soil properties (e.g., C/N ratio and SOC compositions) and geo-environmental factors (e.g., hydro-thermal conditions, pH and Eh, and microbial community, among others). Permafrost C stocks and biodegradability data sets in Circum-Arctic regions have been developed and constructed. Projections of permafrost C feedback to climate warming reveal an accelerated C emission in permafrost regions from abrupt permafrost degradation and intensified or intensifying wildfires in permafrost regions.
Despite quantitative studies on organic carbon stocks and emissions in permafrost regions, the strength and timing of C emission from northern permafrost regions in the future remain evasive. Inadequacies in the estimation of carbon stocks, particularly in subsea permafrost and gas hydrates in and under permafrost, tangle up the extents and rates of permafrost C emissions. Laboratory incubation results for model upscaling are essential to constrain the potentials of permafrost carbon emissions under a warming climate, which are inadequate for current data sets on the decomposability of permafrost carbon. Knowledge of POC decomposability mechanisms seems inadequate. Present-day CO2 and CH4 emissions from northern permafrost regions have not been fully examined, which would be useful to verify modeling results and parameterization. Abrupt permafrost degradation contributes to a large amount of C emission. Aside from thermokarst processes, methane hydrate explosions and wildfire-induced abrupt C feedbacks are also missing from current models. Aquatic systems contribute to one-half of C emissions, of which the stocks of organic carbon and release potentials are often neglected from the existing studies.
According to those mentioned above, several prioritizations of the impact of permafrost degradation on carbon stocks and emissions are underlined here. (1) We suggest to greatly and rapidly improve the reliability for the estimation of C stocks, especially in subsea and gas-hydrate permafrost regions. (2) Laboratory incubation should be widely conducted and related to environmental factors (e.g., microbial abundance and compositions) to establish and improve the permafrost carbon monitoring and incubation network and the associated databanks. (3) Observations of carbon emission in permafrost regions, including through remote sensing and data-miming techniques (e.g., machine learning algorithms) and in situ observations, are essential to verify the modeling performance; and, thus, should be greatly promoted and enhanced. (4) We propose to rapidly and extensively develop observation and modeling networks for abrupt permafrost degradation, such as those involving methane hydrate explosion and wildfire-induced permafrost degradation. (5) We advise to estimate the C loads in aquatic systems and their release potentials for additional carbon feedback to climate warming.

Author Contributions

Writing—original draft preparation, Q.M.; writing—review and editing, H.J.; supervision, H.J.; project administration, H.J.; funding acquisition, H.J. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the Natural Science Foundation of China (NSFC Grant No. 41871052) “Impacts of forest fires in the Da Xing’anling Mountains, Northeast China on the permafrost environment”; Key Program of NSFC Joint Foundation with Heilongjiang Province for Regional Development (Grant No. U20A2082) “Hydrothermal response mechanisms and carbon-cycling impacts of the degrading Xing’an permafrost”; and the Chengdong Leadership Research Funding of Northeast Forestry University (LJ2020-01) “Changes in Xing’an-Baikal permafrost and their impacts”.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors are grateful to Emeritus Stuart A. Harris with the University of Calgary for his generous English editing and careful check in the technicality of this paper. The authors would also like to thank two unidentified reviewers for their insightful suggestions and professional comments in improving the paper.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Thermokarst landscapes, which may also play important roles in carbon cycles in permafrost regions. Notes: (a) Thermokarst ponds near the Hudson Bay, Canada (Source: http://commons.sikimedia.org/wiki/File: Permafrost thaw ponds in Hudson Bay Canada near Greenland. Jpg, (accessed date 13 May 2021)); (b) thermal erosion gully near the Wanlong Worma Lake to the south of the Gyaring Lake in the southcentral Headwater Area of Yellow River on the northeastern Qinghai-Tibet Plateau, Southwest China (Photo by Dr. Qingfeng Wang); (c) coastal erosion and thermal slumps on the Qikiqtaruk-Herschel Island, Arctic Canada [14]; and (d) giant crater or sinkhole possibly formed by methane explosion on the Yamal Peninsula, northwestern Siberia (Source: https://siberiantimes.com/science/casestudy/news/n0415-danger-of-methane-explosions-on-yamal-peninsula-scientists-warn/) (accessed on 21 September 2021).
Figure 1. Thermokarst landscapes, which may also play important roles in carbon cycles in permafrost regions. Notes: (a) Thermokarst ponds near the Hudson Bay, Canada (Source: http://commons.sikimedia.org/wiki/File: Permafrost thaw ponds in Hudson Bay Canada near Greenland. Jpg, (accessed date 13 May 2021)); (b) thermal erosion gully near the Wanlong Worma Lake to the south of the Gyaring Lake in the southcentral Headwater Area of Yellow River on the northeastern Qinghai-Tibet Plateau, Southwest China (Photo by Dr. Qingfeng Wang); (c) coastal erosion and thermal slumps on the Qikiqtaruk-Herschel Island, Arctic Canada [14]; and (d) giant crater or sinkhole possibly formed by methane explosion on the Yamal Peninsula, northwestern Siberia (Source: https://siberiantimes.com/science/casestudy/news/n0415-danger-of-methane-explosions-on-yamal-peninsula-scientists-warn/) (accessed on 21 September 2021).
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Figure 2. Mega-slump in the Batagaika taiga zone, Yana Uplands, eastern Siberia, Russia (revised from [18]).
Figure 2. Mega-slump in the Batagaika taiga zone, Yana Uplands, eastern Siberia, Russia (revised from [18]).
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Figure 3. Changes in fluvial dissolved organic carbon (DOC), particulate organic carbon (PTOC), and dissolved inorganic carbon (DIC) exports in permafrost catchments. Note: The states of permafrost degradation in each estimated catchment are classified as High degree of permafrost degradation (HD), Low degree of permafrost degradation (LD), and Stable permafrost (SP) (data cited from [9,101,105,106,107,108,109,110,111,112]).
Figure 3. Changes in fluvial dissolved organic carbon (DOC), particulate organic carbon (PTOC), and dissolved inorganic carbon (DIC) exports in permafrost catchments. Note: The states of permafrost degradation in each estimated catchment are classified as High degree of permafrost degradation (HD), Low degree of permafrost degradation (LD), and Stable permafrost (SP) (data cited from [9,101,105,106,107,108,109,110,111,112]).
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Table 1. Distribution of soil organic carbon (SOC) in permafrost regions.
Table 1. Distribution of soil organic carbon (SOC) in permafrost regions.
RegionsSoil Horizons
or Depths (m)
Time
Period
Areal Extent
(106 km2)
Soil Organic Carbon Density (kg·m3)Carbon Stock
(Pg C)
References
Latitudinal permafrost regions (1460–1600 Pg C)
Arctic/Antarctic
     Arctic0–0.25present5.618.81~26.33[26]
     High Arctic0–0.3present1.06831.2110 ± 3[1]
     High Arctic0–1present1.06822.4724 ± 8[1]
     High Arctic1–2present1.0686.557 ± 5[1]
     High Arctic2–3present1.0682.813 ± 3[1]
     Yedoma 1>3present1.3874–1758–371[27]
     Yedoma>3LGM 21.3216.32390–446[28]
     Siberian yedoma>3present118450[4]
     Siberian yedoma>3present118.5~407[29]
     Deltaic deposits>3present0.088.3–56.291 ± 52[1]
     Antarctic<1present0.495 0.725[30]
     Antarctic Peninsula<1present0.1 0.6[30]
Circumpolar/boreal/Sub-Arctic regions
     Circum-Arctic regions0–0.3present18.78233.95191.29[29]
     Circum-Arctic regions0–0.3present17.840.64217 ± 12[1]
     Circum-Arctic regions0–1present18.78226.40495.8[29]
     Circum-Arctic regions1–2present17.819.94355 ± 81[1]
     Circum-Arctic regions2–3present17.811.63207 ± 42[1]
     Circum-Arctic regions0–3present18.78218.171024[29]
     Circum-Arctic regions0–3present17.819.381035 ± 150[1]
     Circum-Arctic regions0–3present17.8 1084[31]
     Circum-Arctic regions0–3LGM 129.3 790[31]
     Boreal forest0–3present12.04.17150[32]
     Boreal and subarctic peatland0–1.1present3.4670.9–97.2270–370[33]
     Boreal and subarctic peatland0–2.3present3.34559.14455[32]
     Boreal and subarctic peatland0–3present3.46 457–683[31]
     Boreal and subarctic peatland0–3LGM0.87 30[31]
Elevational permafrost regions (21.7–42.7 Pg C)
Qinghai Tibet Plateau (QTP)
     QTP0–1present1.3512.8117.3 ± 5.3[34]
     QTP0–2present1.357.8527.9 ± 8.0[34]
     QTP0–3present1.353.7833.3 ± 9.4[34]
     QTP>3present1.353.77127.2 ± 37.3[34]
     QTP0–2present1.486.2018.34 ± 7.0[36]
     QTP0–3present1.0611.4536.4 ± 2.5[37]
     QTP0–3present1.724.2021.69[38]
Alpine/mountain regions
     Alps0–1present5 × 10−37–350.04–0.18[39]
     Urals0–0.5present0.137.7–39.30.50–2.55[40]
     Andes0–1present2.6 × 10−2 [1]5.2–88.30.1–2.3[41]
     Altai (Russia)0–1present5.1 × 10−52.0–3.2 [42]
1 Yedoma is an ice-rich loess, with volumetric ice content of 50–90% and organic carbon content of 2–5%, mainly distributed in the northeastern part of North Siberia, Alaska, and Canada; 2 LGM: Last Glacial Maximum (ca. 30–20 ka BP).
Table 2. Models’ information on permafrost carbon feedback on climate warming.
Table 2. Models’ information on permafrost carbon feedback on climate warming.
Coupled ModelsModeling ObjectivesSpatial
Resolution
Temporal
Resolution
Reference
Hydrological and thermal model and biogeochemical modelnet-CO2 flux1.9° × 1.2°1 day[115]
Permafrost model and 1-D soil modelCO2 & CH4 fluxes by degrading permafrost0.5° × 0.5°5 days[116]
ORCHIDEE (Organizing Carbon and Hydrology in Dynamics Ecosystems) model and CH4 modulenet-CO2 and CH4 fluxes1.0° × 1.0°3 h[117,123]
UVic ESCM (University of Victoria Earth System Climate Model) and permafrost modelCO2 flux by permafrost degradation3.6° × 1.8°5 days[118]
LPJmL (Lund–Potsdam–Jena managed Land) model and permafrost moduleNet ecosystem carbon exchange0.5° × 0.5°1 day[119]
Two-dimension multi-pool modelCO2 and CH4 flux by permafrost degradation2.0° × 2.0°1 day[120]
IMOGEN (Integrated Model Of Global Effects of climatic aNomalies)net-CO2 flux2.5° × 3.75°30 min[121]
CLM4.5BGC coupled with 3-D thermokarst lake modelCO2 and CH4 flux by degrading permafrost0.5° × 0.5°1 month[122]
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Jin H, Ma Q. Impacts of Permafrost Degradation on Carbon Stocks and Emissions under a Warming Climate: A Review. Atmosphere. 2021; 12(11):1425. https://doi.org/10.3390/atmos12111425

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Jin, Huijun, and Qiang Ma. 2021. "Impacts of Permafrost Degradation on Carbon Stocks and Emissions under a Warming Climate: A Review" Atmosphere 12, no. 11: 1425. https://doi.org/10.3390/atmos12111425

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