Articles | Volume 23, issue 7
https://doi.org/10.5194/bg-23-2545-2026
© Author(s) 2026. This work is distributed under the Creative Commons Attribution 4.0 License.
Higher tree diversity reduces the likelihood of Amazon tipping points
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- Final revised paper (published on 15 Apr 2026)
- Preprint (discussion started on 04 Sep 2025)
Interactive discussion
Status: closed
Comment types: AC – author | RC – referee | CC – community | EC – editor | CEC – chief editor
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RC1: 'Comment on egusphere-2025-4148', Anonymous Referee #1, 08 Sep 2025
- AC1: 'Reply on RC1', Johanna Van Passel, 09 Feb 2026
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RC2: 'Comment on egusphere-2025-4148', Anonymous Referee #2, 22 Jan 2026
- AC2: 'Reply on RC2', Johanna Van Passel, 09 Feb 2026
Peer review completion
AR – Author's response | RR – Referee report | ED – Editor decision | EF – Editorial file upload
ED: Publish subject to minor revisions (review by editor) (27 Feb 2026) by Manuela Balzarolo
AR by Johanna Van Passel on behalf of the Authors (27 Feb 2026)
Author's response
Author's tracked changes
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ED: Publish as is (24 Mar 2026) by Manuela Balzarolo
AR by Johanna Van Passel on behalf of the Authors (02 Apr 2026)
General comments:
This manuscript titled “Higher tree diversity reduces critical slowing down in the Amazon forest” presents an interesting study investigating the response of the globally most important forest ecosystem to climate change. To this end, the authors simulate changes in tree species diversity and composition under different scenarios varying in spatial (alpha, beta, gamma) scale. Their findings highlight the critical link between biodiversity and ecosystem stability and thus should have important implications for Amazon forest biodiversity conservation.
Generally, I believe that this is an excellent study based on proper statistical analysis given the complexity of the stability and diversity data being investigated across multiple spatial scales. However, I must admit that when reading through the manuscript at times I was a bit confused about the jargon with regard to the hypothesis investigated in this study. For instance, in L55 you refer to the insurance hypothesis by specifically stating “diversity may increase stability by reducing critical slowing down or the likelihood of tipping points.” Later on, in L71 you expect “a positive correlation between diversity and stability, or a negative correlation between diversity and critical slowing down”. Hence, while it is clear what relationship (negative/positive) you are referring to it might still be worth to improve the clarity of a few sentences by following the logic of arguments. Having said this, I would further recommend rephrasing the title to something more intelligible like “Higher tree diversity reduces the likelihood of Amazon tipping points”. While this might represent a minor issue, I would emphasize the need of further clarifying some details with regard to the methodology applied in this study. Specifically, I am not fully convinced about the following points (listed by line numbers): (i) application of temporal autocorrelation (TAC-1), seasonality index (L117-121) and cumulative water deficit (L166-172); (ii) derivation of alpha stability as the negative value of the TAC(+0.1) trend in the EVI time series (135-145); (iii) representation of causal relationships (alpha, beta, gamma) in the conceptual structural equation model (L195 and L259-263).
Specific comments:
First, if I understand correctly you have extracted monthly EVI images from 2001 to 2019 from the daily Moderate Resolution Imaging Spectrometer (MODIS) and used the decomposed remainder (of the seasonal and trend decomposition) to calculate the lag-1 autocorrelation with a moving window length of five years. While I have applied this method myself and do appreciated its value for investigating temporal correlations among biophysical parameters with their environmental drivers, I do wonder why you did not investigate (or at least mention) any other lags (1/3/6/12 months) in the time-series. Usually, one would expect recurring seasonal (e.g., 6 months or annual) pattern between vegetation parameters and climatic drivers (e.g. Hofhansl et al., 2012), which could be investigated by further computing partial autocorrelations and cross-correlation functions (i.e., ACF and CCF, sensu Venables & Ripley 2002).
Second, I can see why you want to avoid a negative number in the denominator of equation (L135) and you mention the additional analysis being based on a subsection of the dataset (and results presented in the appendix A) but I am still not convinced that the resulting values are representative of shifts in ecosystem function (L393). Hence, while I do concur with the assumption that the pattern detected in the analysis is related to signals in remotely sensed EVI patterns and associated shifts in phenology (L390-393) I would expect that this might be related to short-term fluctuations (in mainly canopy characteristics) rather than long-term dynamics (representing shifts in functional species composition) due to tree mortality.
Third, you indicate that the assumptions for linear regression, such as the linearity of the data, normality of the residuals, homogeneity of residuals variance, and independence of the error terms, have been checked, and that none of them were violated (L204-207) but I am still not fully convinced it is feasible to throw in seemingly related variables, such as alpha, beta, gamma diversity into one and the same structural equation model (even when using piecewise SEM and accounting for random effects, such as “region ID” (L212). Given that tree species richness in this study is being based on model predictions rather than plot measurements wouldn’t be alpha, beta, and gamma diversity therefore be auto correlated and thus violate the assumptions of independence anyway?
Having said that, several foregoing studies have highlighted that the Amazon is more likely to experience local transitions to a degraded state in response to multiple and linked environmental and anthropogenic factors (Franco et al., 2025) rather than to result in a systematic break-down (Rammig et al., 2010).
Nevertheless, I do believe that this analysis represents a valuable contribution to the scientific debate about the fate of the Amazon forest in response to both natural and anthropogenic disturbance, but as indicated above, I would recommend adding clarifying details on the applied methodology (see the specific points raised above) and to further stress the underlying aspects regarding the presentation of the study findings so that the reader could follow the line of arguments presented in the main text in a clear and concise manner.
References (to be considered):
Franco, M.A., Rizzo, L.V., Teixeira, M.J. et al. How climate change and deforestation interact in the transformation of the Amazon rainforest. Nat Commun 16, 7944 (2025). https://doi.org/10.1038/s41467-025-63156-0
Hofhansl, F., J. Kobler, J. Ofner, S. Drage, E.-M. Pölz, and W. Wanek (2014), Sensitivity of tropical forest aboveground productivity to climate anomalies in SW Costa Rica, Global Biogeochem. Cycles, 28, 1437–1454, doi:10.1002/2014GB004934
Rammig, A., Jupp, T., Thonicke, K., Tietjen, B., Heinke, J., Ostberg, S., Lucht, W., Cramer, W. and Cox, P. (2010), Estimating the risk of Amazonian forest dieback. New Phytologist, 187: 694-706. https://doi.org/10.1111/j.1469-8137.2010.03318.x
Venables WN, Ripley BD (2002). Modern Applied Statistics with S, series Statistics and Computing. Springer, New York, NY. doi:10.1007/978-0-387-21706-2