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Deficits of biodiversity and productivity linger a century after agricultural abandonment

Nature Ecology & Evolution volume 3, pages 1533–1538 (2019)Cite this article

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Abstract

At the global scale, human activities are threatening the extinction of many species. It remains debated, however, whether there has been corresponding loss of biodiversity at the smaller spatial scales at which species loss often erodes ecosystem functioning, stability and services. Here we consider changes in local biodiversity and productivity over 37 years in 21 grasslands and savannahs with known agricultural land-use histories. We show that, during the century following agricultural abandonment, local plant diversity recovers only incompletely and plant productivity does not significantly recover. By 91 years after agricultural abandonment, despite many local species gains, formerly ploughed fields still had only three quarters of the plant diversity and half of the plant productivity observed in a nearby remnant ecosystem that has never been ploughed. The large and growing extent of recovering ecosystems provides an unprecedented opportunity to reverse the impacts of habitat loss. Active restoration efforts are needed to enable and accelerate recovery.

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Fig. 1: Hypothesized and observed changes in local biodiversity and ecosystem functioning during recent decades.
Fig. 2: Trends in biodiversity, productivity, species richness and species evenness.
Fig. 3: Analyses of temporal and spatial trends in biodiversity.

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Data availability

The plant biomass and cover data that support the findings of this study are available from the Cedar Creek Long-Term Ecological Research project website (www.cedarcreek.umn.edu/research/data).

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Acknowledgements

We thank T. Mielke, K. Worm and the many undergraduate student interns for assistance with field work. We acknowledge funding support from the US National Science Foundation’s Long-Term Ecological Research (LTER) programme (DEB-1831944), the LTER Network Communications Office (DEB-1545288) and an NSF CAREER award (DEB-1845334).

Author information

Authors and Affiliations

  1. Department of Ecology, Evolution and Behavior, University of Minnesota Twin Cities, Saint Paul, MN, USA

    Forest Isbell & David Tilman

  2. Bren School of Environmental Science and Management, University of California, Santa Barbara, Santa Barbara, CA, USA

    David Tilman

  3. Department of Forest Resources, University of Minnesota Twin Cities, Saint Paul, MN, USA

    Peter B. Reich

  4. Hawkesbury Institute for the Environment, University of Western Sydney, Penrith, New South Wales, Australia

    Peter B. Reich

  5. Department of Physiological Diversity, Helmholtz Center for Environmental Research (UFZ), Leipzig, Germany

    Adam Thomas Clark

  6. German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Synthesis Centre for Biodiversity Sciences (sDiv), Leipzig, Germany

    Adam Thomas Clark

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  1. Forest Isbell
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Contributions

D.T. designed and conducted three of the long-term studies (E001, E014 and E154); P.B.R. conducted one of the long-term studies (E133); A.T.C. contributed to data collection; and F.I. conceived this project, contributed to data collection, analysed the data and wrote the paper, with input from all coauthors.

Corresponding author

Correspondence to Forest Isbell.

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The authors declare no competing interests.

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Extended data

Extended Data Fig. 1 Field details for plant biomass data.

Range of years sampled, range of years since agricultural abandonment (YSA), number of years in which sampling occurred, and number of observations for fields sampled in the old field chronosequence study (Cedar Creek study E054) and in the control plots of the long-term fertilization study (Cedar Creek study E001). Field D is the never-plowed primary vegetation reference.

Extended Data Fig. 2 Model selection results.

The most parsimonious model, based on the Akaike Information Criterion (AIC), is bolded for each response variable. In each case, models with linear or decelerating (logarithmic) fixed effects for YSA (years since agricultural abandonment) were first compared. The most parsimonious of these fixed effect structures was retained for subsequent comparisons of alternative random effects and autocorrelation structures. df = degrees of freedom; YSA = years since agricultural abandonment.

Extended Data Fig. 3 Plant species that are near their northern range limit at our study site.

That is, these ten species are found in Minnesota, including at our study site, but not in Manitoba or Ontario, the Canadian Provinces that are more than 350 km north of study site. Gains of these species during our study could possibly be attributable to range shifts in response to climate change. However, 9 of these 10 species were already present at the beginning of these studies, observed in 1982, the first year of observations, or in 1983, the first year of observations in another survey of plants in these fields (E014), or in 1984 in another experiment (E002) that is also located in these same fields. Furthermore, an additional 166 plant species observed in our study are found in Minnesota and in Manitoba or Ontario and thus are not near their northern range limit. Thus, only 1 of the 176 plant species identified in our studies, Aristida tuberculosa, possibly arrived at the study site during recent decades due to a range shift in response to climate change. Even this species may have been present, but failed to be detected, during early years, due to dormancy or observation error.

Extended Data Fig. 4 Introduced species.

The 42 plant species listed here were introduced to Minnesota. About half of these species were already observed in 1982, during the first year of observations. About three quarters of the species were observed by 1988, the first year of the annual sampling of the old field chronosequence (E054). This leaves only 8 of the 176 plant species identified in our studies that possibly arrived at the study site during recent decades due to biotic homogenization resulting from species introductions. Even these eight species may have been present from the start, but failed to be detected, during early years, due to dormancy or observation error.

Extended Data Fig. 5 Field details for plant cover data.

Range of years sampled, number of years in which sampling occurred, and number of observations for fields sampled in the old field chronosequence study that collected plant cover data (Cedar Creek study E014) and in the long-term prescribed fire study that collected plant cover data (Cedar Creek study E133). The Field numbers given for E014 correspond to the Field numbers given for E054 in Extended Data Fig. 1. The Field numbers given for E133 are its plot numbers and do not correspond to the field numbers of E014 or E054.

Extended Data Fig. 6 Spatial comparison of local (0.5 m2) plant species richness between 18 fields that were never-plowed and 26 fields that were formerly-plowed.

Data shown are based on plant cover measurements and were averaged over all observations (quadrats and years) within fields, such that the variation shown is only across fields. Here, rather than having a single never-plowed field as a reference remnant (as in Fig. 2), values are shown as a percentage of the average plant species richness observed in 18 fields that were never-plowed. Note that these percentages are not directly comparable to those shown in Fig. 2 because they were collected by a different method (cover estimates, rather than clipped biomass) and at a different spatial scale (0.5 m2, rather than 0.3 m2). Nevertheless, the results are similar in that, in both cases, formerly-plowed fields tend to have lower local plant species richness than never-plowed fields. Details for each field are provided in Extended Data Fig. 5. Box plots summarize observed data: black band, median; bottom and top of boxes respectively correspond to lower and upper quartiles; error bars show 1.5 times the interquartile range.

Extended Data Fig. 7 Many lands worldwide are now recovering after agricultural abandonment, especially in the regions where most biodiversity monitoring has occurred in recent decades (that is, Northern America and Western Europe).

Decreases in agricultural land area over time indicate that more land is being abandoned from agriculture than is being converted to it. Given that abandoned agricultural lands are now widespread, and that it can take more than a century for recovery of biodiversity following agricultural abandonment (Fig. 2), many species gains observed during recent decades may be the reduction of a biodiversity deficit, rather than a local biodiversity surplus (Fig. 1). Data shown are from the Food and Agriculture Organization (FAO) of the United Nations (www.fao.org/faostat). Agricultural area includes arable land (temporary crops, temporary pastures and hay meadows, gardens), permanent crops (crops that do not need to be replanted after each harvest), and permanent pastures (herbaceous forage crops, either sown or natural vegetation).

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Isbell, F., Tilman, D., Reich, P.B. et al. Deficits of biodiversity and productivity linger a century after agricultural abandonment. Nat Ecol Evol 3, 1533–1538 (2019). https://doi.org/10.1038/s41559-019-1012-1

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