Freshwater lake ecosystem shift caused by social-economic transitions in Yangtze River Basin over the past century

Global lake systems have undergone rapid degradation over the past century. Scientists and managers are struggling to manage the highly degraded lake systems to cope with escalating anthropogenic pressures. Improved knowledge of how lakes and social systems co-evolved up to the present is vital for understanding, modeling, and anticipating the current and future ecological status of lakes. Here, by integrating paleoenvironmental, instrumental and historical documentary resources at multi-decadal scales, we demonstrate how a typical shallow lake system evolved over the last century in the Yangtze River Basin, an urbanized region containing thousands of shallow lakes. We find abrupt ecological shift happened in the lake ecosystem around the 1970s, with the significant reorganization of macrophyte, diatom and cladocera communities. The lake social-ecological system went through three stages as the local society transformed from a traditional agricultural before 1950s to an urbanized and industrialized society during the recent thirty years. The timing and interaction between social, economic and ecological feedbacks govern the transient and long-term dynamics of the freshwater ecosystem. Our results highlight the importance of accounting for the long-term dynamics and feedbacks between ecological, social and economic changes when defining safe operating spaces for sustainable freshwater ecosystem management.

Similar content being viewed by others

Widespread societal and ecological impacts from projected Tibetan Plateau lake expansion

Article 27 May 2024

Mapping global lake dynamics reveals the emerging roles of small lakes

Article Open access 01 October 2022

Effects of climate and land-use changes on fish catches across lakes at a global scale

Article Open access 20 May 2020

Introduction

Freshwater lake ecosystems are among the most valuable and heavily used natural systems worldwide, and they provide important ecosystem services to many millions of people 1,2 . Widespread decline in ecological conditions, loss of biodiversity and dramatic shift in ecosystem structure and function have been reported from different parts of the world 3,4,5 . Scientists and managers face many challenges to manage heavily degraded lake ecosystems. For instance, the effects of natural perturbations and human activities in modern landscapes may be accentuated by events in previous decades or even centuries 6 , and the historical legacy makes it difficult to fully understand the mechanism of current degradation 7 . In some cases, restoration and bringing the ecosystem back to the “references condition” may not be practical as many ecosystems have been irreversibly altered into “novel ecosystems” 8,9 . Further, current socioeconomic constraints related to food production and the livelihood of people within the lake catchment can ultimately complicate the full restoration of freshwater lake ecosystems 10,11 .

A deeper understanding of how social and ecological system co-evolved through time is important for modeling, understanding, and anticipating current and future social-ecological system 12,13 . Long-term perspective can help to observe the nature of legacies and contingencies: such as the slow and fast process 14 , the existence of threshold 15 , and the convergence and divergence of system and variable trajectories 16,17 . These system behaviors can give crucial insight into the functioning of contemporary social-ecological systems 18 . New frameworks and models are emerging for investigating the interaction between long periods of stability and abrupt change in social-ecological systems 19,20 . For instance, Cumming et al. provided a conceptual framework to illustrate how society over-exploit ecosystems through time and leading to “green (sustainable)” or “red (unsustainable)” loops 21 . However, far fewer empirical studies attempt to combine ecological, social and economic perspectives to inform about coupled social-ecological change at multi-decadal scales 22 . The lack of long-term biophysical records is a major barrier, as direct observations from monitoring and survey were usually too short or too limited in scope to provide a comprehensive record 23 . Palaeoenvironmental sciences could provide continuous multi-decadal records for an array of ecosystem states, process and services 13,18,24 . Although there are increasing paleoecological studies examining the effects of land use change on lake ecosystems, fewer studies address these complex interactions from a social-ecological perspective 25,26,27 .

In this study, we take a historical evolutionary approach to generate new insights into the lake ecosystem and social change within the past century, using the Changdang Lake from the Lower Yangtze River Basin as a case study (Fig. 1). The lakes along the low Yangtze River are one of the largest groups of shallow lakes in the world 28 , and this region experienced dramatic social and ecological transition during the last centuries, which exemplifies the changes that have occurred across lake ecosystems globally. More than 80% of lakes examined in this region are seriously degraded and eutrophied 29 . The government has made great efforts to restore the lake’s ecosystem, with little progress so far 30 . Previous attempts have failed because many of them have focused only on the most recent symptoms of the problems rather than on their deep historical cause 31 . Many contemporary studies often seek to explain current conditions by the most recent events only 32,33 . A key challenging facing lake managers in China and elsewhere is to develop a deeper, holistic understanding of lake ecosystem dynamics through time.

figure 1

Here, we integrate paleoenvironmental, instrumental and historical documentary records to examine multi-decadal changes of social-ecological system in Changdang Lake, with two key objectives; (1) Reveal the trajectories of change that have produced the current situation of the lake ecological system; (2) How the interactions, feedback between lake social and ecological systems changed during the last century.

Results

Aquatic community change

Our results revealed substantial changes in macrophyte, zooplankton and phytoplankton communities in Changdang Lake over the last 100 years. We identified more than 20 macrophyte species (for detailed assemblage change, see Fig. S2), which can be classified into three broad groups: emergent, submerged and floating-leaved macrophyte (Fig. 2). Detailed description of aquatic pollen species change has been discussed by Ge et al. 34 . Cluster analysis on these pollen assemblages (Bray-Curtis distance) revealed two significant zones (Fig. S2). The relative abundances of macrophyte assemblages were quite constant and were dominant by the Phragmites type (with an average percentage around 60%) before the 1970s, while the submerged and floating-leaved type macrophyte increasing significantly after the 1970s.

figure 2

Both the diatom and cledoceran were poorly preserved in the lower section bottom of the sediment core, only subsamples in the upper ~25 cm were counted and used for analysis in this study. There were a total of 16 Cledoceran species identified, in which Bosmina dominated the composition of the total cladocerans community up to the 1970s (Fig. S3). However, littoral species increased significantly since the 1970s, from 40% to nearly 80% around 1980s, which are dominated by Chydorus sphaericus. Diatom assemblages also showed clear change since 1970 (Fig. S4). The epiphytic taxa Cocconeis placentula (up to 60%) and the benthic Fragilaria construnes (up to 20%) dominated the diatom community between 1970 and 1980. Both of them declined substantially after 1980. The planktonic taxa increased significantly since 1980, characterized by Cyclotella meneghiniana, Aulacoseira ambigua. Facultative planktonic Aulacoseira ambigua reached its peak value around the 1990s.

Environmental factors

Profiles of trace metals exhibited a broadly consistent pattern of variability (Fig. 2). Their values remained near the background levels prior to the 1970s, increased rapidly between 1970 and 1980, and subsequently decreased towards the sediment-water interface. All variables including total organic carbon (TOC), total phosphorus (TP), and total nitrogen (TN) in lake sediments were relatively stable from 1890 to 1970. However, all these variables increased abruptly between 1970 and 1980 and then kept at a relative stable level. The magnetic susceptibility (MS) and grain size of the large particle (>64 um) both showed relatively low and stable values between 1900 and 1970s and then increased abruptly during the 1970s with high variability (Fig. 2).

Regime shift detection and pressure- response relationship

For the aquatic macrophyte community, the first two ordination axes (PC1 and PC2) explained 58% of the variation in the aquatic pollen data set. The phase plot of the first two PCs showed two clear regimes (Fig. 3). The PC1 transition points identified by STARS were identified around the 1970s. The result from the constrained cluster analysis and CUSUM of PC1 also complemented the STARS results. The results from the STARS algorithm on PC1 of diatom and cladoceran communities also showed clear transition point between 1970 and 1980 (Fig. S5). Results from the STARS algorithms on grain size, MS, and PC1 of trace metals all identified significant breakpoint around the 1970s, though with slightly time differences (Table S1). In the generalized additive model, the aquatic assemblages (PCA1) show nonlinear relationships with grain size (F = 21.33, P < 0.001, edf = 2.65) and MS (F = 44.84, P < 0.001, edf = 7.48 corresponding to a simple sigmoid curve) (Fig. 4).

figure 3

figure 4

Discussion

Lake environment variability and abrupt ecosystem change

The analysis of multi-proxy indicators has contributed to the development of a robust reconstruction of ecosystem dynamics at the Changdang Lake over the past century. Before the 1970s, Changdang Lake was probably surrounded by an emergent macrophytic belt composed of Typha sp. and Phragmites sp. (Fig. S2) communities, while the submerged and floating-leaved macrophytic communities were relatively poor. The phytoplankton and zooplankton communities were not well developed as suggested by very low diatom and cladoceran concentrations. The lake was probably in an oligotrophic condition with low primary production. The changing frequency and magnitude of other environmental indicators (e.g. trace metals, TP, grain size, and magnetic susceptibility) also suggest relatively less anthropogenic disturbance and natural fluctuation of hydrological conditions of the lake environment. Arguably, the Changdang Lake may have stayed within its long-term historical variability prior to the 1970s (Fig. 2).

After the 1970s, the lake experienced a major transition with significant restructuring and reorganization of aquatic ecosystems, characterized by a sudden shift of the macrophyte, diatom, and cladoceran assemblages. The submerged and floating-leaved macrophytes began to expand quickly, along with an increasing abundance of benthic and epiphytic diatom species. A strong increase in the primary production was reflected by a rapid increase in the concentration of TOC and short and middle chain of n-alkane (Fig. 2). The temporal asynchrony of the abrupt change between different aquatic groups in the lake were probably due to complex biotic interactions 35 . High magnetic susceptibility suggests that increasing catchment erosion in the Changdang Lake, which may have been caused by anthropogenic activities, such as land reclamation and agricultural intensification. The increase of coarse grain size probably indicates the reduced flood energies and more stable water environment which enable large particle size from the local catchment to be deposited 36 . The sudden increase of TP and TN concentration suggest high nutrient loads, contributing to the growth of submerged macrophytes. Further, the increase in the nutrient levels many have led to the proliferation of algal and zooplankton communities. Both the submerged and emergent macrophyte declined gradually from the late 1980s, with increased planktonic diatoms species. This indicates a further degradation of the lake’s aquatic ecosystems.

The sudden shift of ecological structure, together with abrupt hydrological regime change during the 1970s, indicates a set of major environmental disturbances occurring around the lake. The results from the generalized additive model (Fig. 4) suggest that the aquatic communities variation responded to external disturbances in nonlinear ways. More than 20% of the lake area was reclaimed for agriculture land around the 1970s 37 . Widespread river regulation and construction of sluices and reservoirs within the catchment in the early 1970s substantially altered the peak flows and lake hydrology. For instance, about 20 new watercourses with dams and over 50 new water gates built along the Danjingcao River during the 1970s significantly altered the hydrologic process of Changdang Lake 37 . Stable hydrological conditions could reduce the suspension of sediments, enhancing water transparency and benefiting the development of macrophytes 38 . Similar biotic responses to reduced hydrological dynamics were also reported in the lower Yangtze regions 39,40 . Meanwhile, the increased nutrient loads from the catchment stimulated the proliferation of phytoplankton and zooplankton. Eutrophication was further amplified by industrial developments and the intensive aquaculture practices. Expansion of local industrial factories across the catchments further affected the water quality directly because of untreated sewage inputs into the lakes. Aquaculture with extensive fish cage cultures in the lake expanded to more than half of the lake area from the late 1970s 37 .

Climate change superimposed on these anthropogenic stressors and exacerbate the degraded condition further. Annual mean temperature in this region increased 1.52 °C during 1909–2010 41 . Increasing temperature has exacerbated the symptoms of eutrophication through its impact on algal productivity, water column oxygen concentrations, and nutrient recycling 42 . Overall, it is difficult to attribute any single stressor to cause the lake ecosystem shift; rather, multiple disturbances may have acted together in driving this transition.

Dynamics of linked social-ecological systems

The increased nutrient loading, land reclamation, and hydrological modifications are the proximate drivers that directly triggered the shift in lake ecosystems, which is very common in many lakes within the Yangtze River Basin 29,43 . However, these proximate interactions are embedded in a much broader socioeconomic context. By integrating the historical records of societal and economic development in this region (Fig. 5), we argue that the social-ecological system went through a series of phases with complex nonlinear social and ecological interactions and feedback mechanisms (Fig. 6).

figure 5

figure 6

Before 1950, there was a traditional agricultural society within the Changdang lake catchment. More than 90% of the population in this region was directly employed in agricultural food production in early 1950 in Jintan County 37 . Most households relied directly on ecosystem services (fish, crops etc.) for food from local ecosystem through traditional farming and fishing 44 . Farmers produced and consumed their own food and fuels at the local scale. The interactions and feedback between lake ecosystem and human well-being via ecosystem services are relatively clear and easily understood (Fig. 6). The local equilibrium between resource use and human demand was maintained, and the anthropogenic influence on local lake ecosystem was relatively low due to low population density and limited technological development.

Population grew quickly after 1950 with increasing demand for food and resources. This caused large-scale land reclamation and hydrological modifications across the lake catchment. Meanwhile, the adoption of high-yielding technologies (fertilizer and pesticide usage, cage aquaculture) caused serious damage to the lake environment. Other non-agriculture activities, such as heavy industry expanded rapidly during this period taking many people out of agriculture-related work (Fig. 5d). The living standards have soared, and the local income has increased 11 fold during 1950–1985 37 . As a result, agriculture no longer limits the opportunities of rural households. Although the proportion of people who extracted goods directly from ecosystems (farmers, fishers) declines 37 , the resource demand increased quickly as society becomes wealthier. The consumption of fish and meat has increased 16 and 30 fold, respectively, from 1950 to 1980 37 . Local ecosystems are heavily exploited to fulfill the increasing demands of both rural and new urban people. A new feedback between society and lake ecosystem has emerged due to the rapid socio-economic change (Fig. 6).

Industrialization and urbanization developed very quickly during the past 30 years around the Changdang Lake catchment. Small villages and cities in the region have grown rapidly and merged into one of the world’s largest “megapolitan regions”. The society has transformed from an agricultural to an industrialized and urban society. Provisioning services from local ecosystems can no longer meet local demand, and many resources that were formerly met by local ecosystem are outsourced, resulting in an increase in the geographic extent of supply and demand. For instance, the transportation of goods has increased seven-fold from 1970 to 2007 in the Jintan County (Fig. 5c). Consequently, the connection between food production and food consumption has become less apparent, and society is now unintentionally placing increasing pressure on dwindling resources. The dominant feedback has changed from conventional farmer-ecosystem feedback to newly formed socio-economic and ecosystem feedback (Fig. 6). The contemporary Changdang lake ecosystem is not only impacted by local society within the catchment system but is also influenced indirectly at large regional scale through tele-coupling connections due to the market and globalization 45 .

Management implications

Environment managers and policy-makers have a long tradition of regulating the human–environment interface with rules assuming the ecological freshwater systems, and the social systems dependent on them, are relatively linear and stable. Our analysis of the complex interactions between ecological, social, and economic systems over the past century provides several key insights for lake managers and policy-makers. First, it is impossible to understand the persistent ecosystem degradation without explicitly accounting for the interactions between the multiple dimensions of social-ecological systems at multi-decadal timescales. Though it is crucial for managers to focus on reducing direct drivers (e.g. nutrient input) to restore degraded lakes, it is also important to recognize how multiple drivers interact and create a cumulative effect, so that intervention can be targeted appropriately. Second, policy and management strategies also need to accept the likelihood that some ecosystems have changed permanently to a different configuration and fully incorporate threshold and regime shift in lake restoration and conservation 46 .

Furthermore, the long-term social-ecological trajectories and ecosystem feedback mechanisms need to be fully recognized in order to make appropriate management strategies. In the Lower Yangtze Basin, population expansion, increasing wealth and resource demands are the root causes of long-term lake ecosystem degradation. Simplistic approaches based solely on conventional natural sciences that ignore social and economic linkages are doomed to failure. For example, although the restoration of lakes to clear water conditions by reducing nutrients would is theoretically possible, the failure of considering the complex social-ecological interactions and feedbacks would create a huge social burden: the consequences for agricultural yields in the surrounding catchment may be too high to warrant the financial investment and social costs. A focus on ecological functions, ecosystem services, and human drivers, therefore, opens many more possibilities for active management intervention. Ultimately, we need to recognize that improved resource use efficiency, public environmental education, and awareness are fundamentally important for long-term sustainable lake management.

Conclusion

In this study, we illustrate how a better understanding of the linkages between ecological and social systems at multi-decadal scales can generate critical insights for sustainable lake management. Our paleoenvironmental analysis shows abrupt shifts in the macrophyte and planktonic communities around the 1970s in the Changdang Lake. The ecological shift was corresponding to significant social and economic transition as the society transformed from traditional agricultural-base society to an industrialized and urbanized society. Rapid population and market growth, coupled with technological and policy changes, acted to intensify the direct drivers - pollution, hydrological modification and land reclamation - ultimately resulting in the shift of the Changdang lake ecosystem. These linkages - between the demands of people and dynamics of lake ecosystem - highlight the necessity of an interdisciplinary focus for effective management of lake ecosystems from a long-term perspective.

Methods

Study region

Changdang lake (N31°30′-31°40′, E119°30′–119°40′) is a typical shallow freshwater (mean depth 1.2 m) lake, located in the lower Yangtze River Basin, which is the most densely populated and rapidly urbanized area in China (Fig. 1). The lake area is 89 km 2 with a drainage area of 2100 km 2 . More than 20 rivers feed into the lake and some cross the Jintan City which is 9 km away from the lake. The social and economic situation has changed dramatically in this region in the last 50 years. Population in the area has increased from 0.28 million in early 1940 to 0.55 million in 2016, and industrial output has increased from 2 million to 44 billion RMB from 1949 to 2007 37 . The rapid economic development in this region has resulted in rapid urbanization and industrialization within the Changdang lake catchment, which has had an adverse environmental impact on this lake, and others in this region 47 .

Sample collection and Chronology

A 50 cm long sediment core was taken from the center of the Changdang Lake with a gravity corer in 2016 (Fig. 1). The core was subsampled at 0.5 cm resolution. Chronological sequences were constructed based on the radioactivities of bulk sediment 210 Pb and 137 Cs measured by nondestructive gamma spectrometry. 210 Pbex generally shows an exponential distribution in the sediment core, and the increasing trend of 210 Pbex in the upper 5 cm indicate the sediment underwent mixing or bioturbation (Fig. S1). Thus, we use the constant initial concentration model to estimate the sedimentation rate and subsequently establish an age-depth chronology. The average sedimentation rate was 0.45 cm/year and the core covers 111 years (1905–2016). Detailed chronological result has been described in Zhang et al. 48 .

Pollen, Diatom and Cladoceran analysis

Pollen samples were prepared for pollen analysis following the standard acetolysis procedure of Faegri and Iversen 49 , including 10% HCl and 10% NaOH to remove carbonate and organic matter, respectively. Then they were treated by heavy liquid flotation and sieving to get rid of other impurities, acetolysis to eliminate protoplasm in pollen grains and the final preservation in glycerin. All pollen and spores were identified under light microscope with a magnification of 400X. aquatic taxa abundance was expressed with percentages.

Diatom samples preparation followed the standard procedures using the water bath technique 50 . 2 ~ 3 g freeze-dried sediment was treated with 30% H2O2 in water bathing at 85 °C, and the addition of 10% HCl to remove any carbonates. As diatoms were poorly preserved in the lower section bottom of the sediment core, only subsamples in the upper 20 cm were counted. A total of 20 samples were analyzed, and at least 300 valves were counted for each sample. Species abundance was expressed with percentages.

Cladoceran analysis followed the standard procedures 51 . Approximately 2 g dry sediment of each subsample were treated with 10% KOH solution, and heated at 60 C on a hotplate for at least 45 min. Sieving of the subsample mixture was carried out through a 38μm mesh. As Cladoceran were poorly preserved in the lower section of the sediment core, only subsamples in the upper 25 cm were counted. A total of 25 samples were analyzed, and at least 300 identifiable cladoceran remains were counted for each sample. Species abundance was expressed with percentages.

Geochemistry analysis

Metal elements (Al, Fe, Li, K, Mg, Cr, Cu, Zn, Sr) and total phosphorus (TP) were analysed using an inductively coupled plasma-atomic emission spectrometry (ICP-AES). The CE-440 elemental analyzer (EAI Company) was used for the determination of total organic carbon (TOC) and TN content of the samples. Magnetic susceptibility (MS) was measured using a Bartington MS2C sensor. Grain size spectra of samples were determined using a Malvern automated laser optical particle-size analyzer (Mastersixer-2000). All the experiment analyses were carry out at the State Key Laboratory of Lake Science and Environment, Chinese Academy of Sciences.

Social and economic data collection

The social and economic data of Jintan County during the last 100 year (mainly between 1949–2016) were collected from the statistic yearbook, historical document, and local county gazetteers.

Statistical approaches

We employed multiple approaches to detecting the potential regime shifts of lake ecosystem changes. The Sequential T-test Analysis of Regime Shifts algorithm (STARS) devised by Rodionov 50,52 was combined with classical multivariate techniques to identify statistically significant changes in the means of the paleoenvironmental temporal series. For univariate data (e.g. total organic carbon (TOC), MS), the STARS algorithm could be applied directly; while for the multivariate data (e.g. pollen, diatom, cladocero), a principal component analysis (PCA) was first used to extract major components in assemblage variation, and the algorithm was applied on the first principle component axes (PC1). Furthermore, constrained cluster analysis (Bray-Curtis dissimilarity) and a cumulative sum of differences (CUSUM) 53 of these temporal variables were also run to complement with the STARS results. We also applied general additive model 54 to investigate the relationship between aquatic macrophyte community dynamics and local anthropogenic disturbance proxies (grain size and MS).

Data Availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

References

  1. Reynaud, A. & Lanzanova, D. A Global Meta-Analysis of the Value of Ecosystem Services Provided by Lakes. Ecological Economics137, 184–194, https://doi.org/10.1016/j.ecolecon.2017.03.001 (2017). ArticlePubMedPubMed CentralGoogle Scholar
  2. Beklioğlu, M. et al. Preface: Shallow lakes in a fast changing world. Hydrobiologia778, 9–11, https://doi.org/10.1007/s10750-016-2840-5 (2016). ArticleGoogle Scholar
  3. Kafumbata, D., Jamu, D. & Chiotha, S. Riparian ecosystem resilience and livelihood strategies under test: lessons from Lake Chilwa in Malawi and other lakes inAfrica. Philosophical Transactions of the Royal Society B: Biological Sciences 369, https://doi.org/10.1098/rstb.2013.0052 (2014). ArticleGoogle Scholar
  4. Smol, J. P. et al. Climate-driven regime shifts in the biological communities of arctic lakes. Proceedings of the National Academy of Sciences of the United States of America102, 4397–4402, https://doi.org/10.1073/pnas.0500245102 (2005). ArticleADSCASPubMedPubMed CentralGoogle Scholar
  5. Zhang, Y. et al. Global loss of aquatic vegetation in lakes. Earth-Science Reviews173 (2017). ArticleCASGoogle Scholar
  6. Petty, A. M. et al. Applying historical ecology to natural resource management institutions: Lessons from two case studies of landscape fire management. Global Environmental Change31, 1–10, https://doi.org/10.1016/j.gloenvcha.2014.11.004 (2015). ArticleADSGoogle Scholar
  7. Ramstack Hobbs, J. M. et al. The legacy of large regime shifts in shallow lakes. Ecological Applications, n/a–n/a, https://doi.org/10.1002/eap.1382 (2016). ArticleGoogle Scholar
  8. Hobbs, R. J., Higgs, E. & Harris, J. A. Novel ecosystems: implications for conservation and restoration. Trends in Ecology & Evolution24, 599–605, https://doi.org/10.1016/j.tree.2009.05.012 (2009). ArticleGoogle Scholar
  9. Kopf, R. K., Finlayson, C. M., Humphries, P., Sims, N. C. & Hladyz, S. Anthropocene Baselines: Assessing Change and Managing Biodiversity in Human-Dominated Aquatic Ecosystems. BioScience65, 798–811, https://doi.org/10.1093/biosci/biv092 (2015). ArticleGoogle Scholar
  10. Jenny, J. P. et al. Global spread of hypoxia in freshwater ecosystems during the last three centuries is caused by rising local human pressure. Global Change Biology22, 1481–1489, https://doi.org/10.1111/gcb.13193 (2016). ArticleADSPubMedGoogle Scholar
  11. Zhang, K., Dearing, J. A., Tong, S. L. & Hughes, T. P. China’s Degraded Environment Enters A New Normal. Trends in Ecology & Evolution31, 175 (2016). ArticleGoogle Scholar
  12. Dearing, J. A. et al. Navigating the perfect storm: Research strategies for social ecological systems in a rapidly evolving world. Environmental Management49, 767–775, https://doi.org/10.1007/s00267-012-9833-6 (2011). ArticleADSGoogle Scholar
  13. Verstraeten, G. Quantification of human–environment interactions in the past. Anthropocene8, 1–5, https://doi.org/10.1016/j.ancene.2015.06.002 (2014). ArticleGoogle Scholar
  14. Walker, B. H., Carpenter, S. R., Rockstrom, J., Crépin, A. S. & Peterson, G. D. Drivers, slow variables, fast variables, shocks, and resilience. Ecology and Society17 (2012).
  15. Larsen, S. & Alp, M. Ecological thresholds and riparian wetlands: an overview for environmental managers. Limnology16, https://doi.org/10.1007/s10201-014-0436-1 (2015). ArticleGoogle Scholar
  16. Willis, K. J., Bennett, K. D., Burrough, S. L., Macias-Fauria, M. & Tovar, C. Determining the response of African biota to climate change: Using the past to model the future. Philosophical Transactions of the Royal Society B: Biological Sciences368, https://doi.org/10.1098/rstb.2012.0491 (2013). ArticleCASGoogle Scholar
  17. Birks, H. J. B. Ecological palaeoecology and conservation biology: Controversies, challenges, and compromises. International Journal of Biodiversity Science, Ecosystems Services and Management8, 292–304, https://doi.org/10.1080/21513732.2012.701667 (2012). ArticleGoogle Scholar
  18. Dietl, G. P. et al. Conservation Paleobiology: Leveraging Knowledge of the Past to Inform Conservation and Restoration. Annual Review of Earth and Planetary Sciences43, 79–103, https://doi.org/10.1146/annurev-earth-040610-133349 (2015). ArticleADSCASGoogle Scholar
  19. Levin, S. et al. Social-ecological systems as complex adaptive systems: Modeling and policy implications. Environment and Development Economics18, 111–132, https://doi.org/10.1017/S1355770X12000460 (2013). ArticleGoogle Scholar
  20. Polhill, J. G., Filatova, T., Schlüter, M. & Voinov, A. Modelling systemic change in coupled socio-environmental systems. Environmental Modelling and Software75, 318–332, https://doi.org/10.1016/j.envsoft.2015.10.017 (2016). ArticleGoogle Scholar
  21. Cumming, G. S. et al. Implications of agricultural transitions and urbanization for ecosystem services. Nature515, 50–57, https://doi.org/10.1038/nature13945 (2014). ArticleADSCASPubMedGoogle Scholar
  22. Dearing, J. et al. Social-ecological systems in the Anthropocene: the need for integrating social and biophysical records at regional scales. The Anthropocene Review, https://doi.org/10.1177/2053019615579128 (2015). ArticleGoogle Scholar
  23. Kidwell, S. M. Biology in the Anthropocene: Challenges and insights from young fossil records. Proceedings of the National Academy of Sciences of the United States of America112, 4922–4929, https://doi.org/10.1073/pnas.1403660112 (2015). ArticleADSCASPubMedPubMed CentralGoogle Scholar
  24. Jeffers, E. S., Nogué, S. & Willis, K. J. The role of palaeoecological records in assessing ecosystem services. Quaternary Science Reviews112, 17–32, https://doi.org/10.1016/j.quascirev.2014.12.018 (2015). ArticleADSGoogle Scholar
  25. Seddon, A. W. R. et al. Looking forward through the past: Identification of 50 priority research questions in palaeoecology. Journal of Ecology102, 256–267, https://doi.org/10.1111/1365-2745.12195 (2014). ArticleGoogle Scholar
  26. Costanza, R. et al. Developing an Integrated History and future of People on Earth (IHOPE). Current Opinion in Environmental Sustainability4, 106–114, https://doi.org/10.1016/j.cosust.2012.01.010 (2012). ArticleGoogle Scholar
  27. Bunting, L. et al. Increased variability and sudden ecosystem state change in Lake Winnipeg, Canada, caused by 20th century agriculture. Limnology and Oceanography61, 2090–2107, https://doi.org/10.1002/lno.10355 (2016). ArticleADSCASGoogle Scholar
  28. Wang, S. M. D., H.S. Lakes of China. (Beijing Science Press, 1998).
  29. Wang, S. R. Lake environment evolution and protection management. (Beijing: Science Press, 2015).
  30. Meng, W. et al. Status of wetlands in China: A review of extent, degradation, issues and recommendations for improvement. Ocean & Coastal Management146, 50–59, https://doi.org/10.1016/j.ocecoaman.2017.06.003 (2017). ArticleGoogle Scholar
  31. Le, C. et al. Eutrophication of lake waters in China: cost, causes, and control. Environmental Management45, 662 (2010). ArticleADSCASGoogle Scholar
  32. Wang, S. R. et al. Ecological security problems of the major key lakes in China. Environmental Earth Sciences74, 3825–3837, https://doi.org/10.1007/s12665-015-4191-3 (2015). ArticleGoogle Scholar
  33. Fu, J. & Fu, J. Issue of cyanobacteria blooms in Taihu Lake, China. Journal of Environmental Science & Management19, 99–109 (2016). Google Scholar
  34. Ge, Y., Zhang, K. & Yang, X. Long-term succession of aquatic plants reconstructed from palynological records in a shallow freshwater lake. Science of The Total Environment643, 312–323, https://doi.org/10.1016/j.scitotenv.2018.06.203 (2018). ArticleADSCASPubMedGoogle Scholar
  35. Rooney, N., Mccann, K., Gellner, G. & Moore, J. C. Structural asymmetry and the stability of diverse food webs. Nature442, 265–269 (2006). ArticleADSCASGoogle Scholar
  36. Yang, S. L. et al. Downstream sedimentary and geomorphic impacts of the Three Gorges Dam on the Yangtze River. Earth-Science Reviews138, 469–486 (2014). ArticleGoogle Scholar
  37. Meng, J. Y. C., X,M. Jintan County Annals. (Jiangsu People’s Publishing, 1993).
  38. Sayer, C. D. et al. Long-term dynamics of submerged macrophytes and algae in a small and shallow, eutrophic lake: implications for the stability of macrophyte-dominance. Freshwater Biology55, 565–583, https://doi.org/10.1111/j.1365-2427.2009.02353.x (2010). ArticleCASGoogle Scholar
  39. Kong, X. et al. Hydrological regulation drives regime shifts: evidence from paleolimnology and ecosystem modeling of a large shallow Chinese lake. Glob Chang Biol, https://doi.org/10.1111/gcb.13416 (2016). ArticleADSGoogle Scholar
  40. Kattel, G. R., Dong, X. & Yang, X. A century-scale, human-induced ecohydrological evolution of wetlands of two large river basins in Australia (Murray) and China (Yangtze). Hydrol. Earth Syst. Sci.20, 2151–2168, https://doi.org/10.5194/hess-20-2151-2016 (2016). ArticleADSGoogle Scholar
  41. Cao, L. et al. Instrumental temperature series in eastern and central China back to the nineteenth century. Journal of Geophysical Research: Atmospheres118, 8197–8207 (2013). ADSGoogle Scholar
  42. Baig, S. A. et al. Impact of climate factors on cyanobacterial dynamics and their interactions with water quality in South Taihu Lake, China. Chem. Ecol.33, 76–87, https://doi.org/10.1080/02757540.2016.1261122 (2017). ArticleGoogle Scholar
  43. Qin, B. et al. Lake eutrophication and its ecosystem response. Chinese Science Bulletin58, 961–970, https://doi.org/10.1007/s11434-012-5560-x (2013). ArticleADSCASGoogle Scholar
  44. Ellis, E. C. & Wang, S. M. Sustainable traditional agriculture in the Tai Lake Region of China. Agriculture Ecosystems & Environment61, 177–193, https://doi.org/10.1016/s0167-8809(96)01099-7 (1997). ArticleGoogle Scholar
  45. Liu, J. et al. Systems integration for global sustainability. Science347, https://doi.org/10.1126/science.1258832 (2015). ArticleGoogle Scholar
  46. Gillson, L. & Marchant, R. From myopia to clarity: sharpening the focus of ecosystem management through the lens of palaeoecology. Trends in Ecology & Evolution29, 317–325, https://doi.org/10.1016/j.tree.2014.03.010 (2014). ArticleGoogle Scholar
  47. Wang, F. L. & Chen, X. P. XH A study on the nutrition status evaluation and algal limiting factor in Lake Changdagn over the last 15 years. Environmental Science &Technology35, 353–357 (2012). Google Scholar
  48. Zhang, Y. D. et al. Sedimentary lipid biomarker record of human-induced environmental change during the past century in Lake Changdang, Lake Taihu basin, Eastern China. Science of the Total Environment613, 907–918, https://doi.org/10.1016/j.scitotenv.2017.09.185 (2018). ArticleADSCASPubMedGoogle Scholar
  49. Fægri, K. & Iversen, J. A Textbook of Pollen Analysis. Journal of BiogeographyIV, (328 (1989). Google Scholar
  50. Battarbee, R. W. et al. Diatoms. Tracking Environmental Change Using Lake Sediments3, 155–202 (2001).
  51. Szeroczyńska, K. S.-K., K. Atlas of Subfossil Cladocera from Central and Northern Europe. (Tow Przyj Dolnej Wisły, Świecie, 2007).
  52. Rodionov, S. N. Use of prewhitening in climate regime shift detection. Geophysical Research Letters33, https://doi.org/10.1029/2006gl025904 (2006).
  53. Nicholls, K. H. CUSUM Phytoplankton and Chlorophyll Functions Illustrate the Apparent Onset of Dreissenid Mussel Impacts in Lake Ontario. Journal of Great Lakes Research27, 393–401, https://doi.org/10.1016/S0380-1330(01)70655-7 (2001). ArticleGoogle Scholar
  54. Simpsona, G. L. & Anderson, N. J. Deciphering the effect of climate change and separating the influence of confounding factors in sediment core records using additive models. Limnology & Oceanography54, 2529–2541 (2009). ArticleADSGoogle Scholar

Acknowledgements

This work was supported by National Basic Research Program of China (NBRPC (#2017YFA0605200), Science Fund for Creative Research Groups of the National Natural Science Foundation of China (#41621002), the National Natural Science Foundation of China (NSFC) (#41530753 and #41772378), and One Hundred Talent Program” of the Chinese Academy of Sciences (#Y6SL011001 to Zhang Ke).

Author information

Authors and Affiliations

  1. State Key Laboratory of Lake Science and Environment, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences, Nanjing, 210008, China Ke Zhang, Xiangdong Yang, Qi Lin & Ji Shen
  2. Environmental Hydrology and Water Resources Group, Department of Infrastructure Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia Giri Kattel
  1. Ke Zhang