Abstract
Globally, our knowledge on lake fisheries is still limited despite their importance to food security and livelihoods. Here we show that fish catches can respond either positively or negatively to climate and land-use changes, by analyzing time-series data (1970–2014) for 31 lakes across five continents. We find that effects of a climate or land-use driver (e.g., air temperature) on lake environment could be relatively consistent in directions, but consequential changes in a lake-environmental factor (e.g., water temperature) could result in either increases or decreases in fish catch in a given lake. A subsequent correlation analysis indicates that reductions in fish catch was less likely to occur in response to potential climate and land-use changes if a lake is located in a region with greater access to clean water. This finding suggests that adequate investments for water-quality protection and water-use efficiency can provide additional benefits to lake fisheries and food security.
Similar content being viewed by others
Introduction
Lakes, natural and man-made, are important reserves of accessible freshwater and are frequently managed for provisioning ecosystem services1, such as drinking water, irrigation, hydropower generation, and fisheries2. Consequently, biota in lake ecosystems could be subject to stressors associated with human activities, such as water withdrawal, floodplain development, exotic species introduction, and overexploitation3. Two important sources of anthropogenic stressors are climate and land-use changes, which may alter a lake ecosystem directly through changing water temperature (WT) and water level (WL), and indirectly through the balance between inputs and outputs of nutrients and sediments, as well as changes in food-web dynamics4,5.
Among lake ecosystem services, fisheries are especially vulnerable to environmental changes because fish are ectothermic and fish distribution is usually limited by structural6, thermal7, and chemical8 barriers. Environmental changes driven by climate and land-use changes have been linked to major shifts in fish catches (CATCHs) and species composition in many lakes around the world, such as lakes Erie9, Kinneret10, Naivasha11,12, Peipsi13, and Victoria14, as well as the collapse of Aral Sea fisheries15. Reduced lake CATCHs caused by climate and land-use changes can threaten food security and livelihoods of millions of people worldwide, especially in impoverished countries where rural poor communities may not have appropriate alternative sources of animal protein and employment opportunity16.
Due to their protracted and compounding nature, understanding the effects of climate and land-use changes on lake CATCHs requires long-term data, which may include climate and land-use data at a spatial scale of the whole catchment (or drainage basin) and environmental, biological, and fishery data at a spatial scale of the whole lake. This intensive data requirement has restricted assessments of how lake environment and lake CATCHs respond to climate and land-use changes to lakes in a few data-rich regions, mostly located in North America and Europe17,18. As a result, given the large number (>1.43 million) of lakes19 and their diversity in size, productivity, species composition, and fisheries6, our current understanding of how changing climate and land-use influences lake CATCHs is very limited at a global scale and is generally lacking for lakes in Africa and Asia where CATCHs are the largest (Supplementary Fig. 1).
The goal of this study is to understand how climate and land-use changes affect lake CATCHs at a global scale. We use a Bayesian networks modeling approach20 to analyze time-series data for the 31 study lakes (Fig. 1) over the period 1970–2014. We choose this modeling approach because it can minimize negative effects of data limitations on the statistical power of our analysis, by accounting for our prior understanding of multi-level, causal processes that could underlie changes in CATCHs in response to changes in climate and land use across lakes. Our Bayesian networks model (BNM) represents the hypothesized causal processes by expressing them as conditional probabilistic relationships between model variables at multiple levels: between climate and land use (operating at a catchment scale) and lake environment21,22,23,24,25,26, and between lake environment and (total) fish biomass27,28,29,30,31,32,33 and thus (total) CATCH34, as shown in Fig. 2. Due to the regional difference in data availability, our study lakes and study period are selected to ensure that we can include approximately equal numbers of study lakes in Africa, the Americas, Asia, and Europe and in both tropic and temperate regions (Fig. 1). The study lakes are diverse in terms of both socio-economic environment and hydrogeomorphology (Supplementary Data 2). However, most study lakes in Europe and the Americas have a better socio-economic environment than the study lakes in Asia and Africa. The diversity of these lakes allows us to identify the characteristics of lakes where CATCHs can be vulnerable to climate and land-use changes, which has implications for identifying vulnerable lake fisheries around the globe.
We conduct three analyses in this study. First, we determine how the climate and land-use drivers affect CATCHs across the 31 study lakes in 1970–2014 by estimating coefficients of our BNM. Second, by implementing the resulting BNM, we run simulations to assess the change in each of climate and land-use drivers associated with a (simulated) 25% decrease in CATCH from the 1970–2014 median (hereafter, a 25% catch decrease) in each lake. Third, we conduct a correlation analysis to identify whether any socio-economic characteristic(s) associated with the catchment or hydrogeomorphological characteristic(s) of the lake corresponded to the magnitudes of changes in any of the climate and land-use drivers that were associated with a 25% catch decrease. To improve clarity, Fig. 3 presents a flowchart that summarizes the procedures of these three analyses and Table 1 provides a list of symbols used in the development of BNM.
We demonstrate that climate and land-use changes can have strong effects on CATCHs across lakes at a global scale, but the effects can be either positive or negative. The subsequent correlation analysis shows that a lake located in a region with greater access to clean water less likely experiences a substantial decrease in CATCH in response to potential climate and land-use changes. These results suggest that investments made for water-quality protection and water-use efficiency can also provide benefits to lake fisheries and food security.
Results
How climate and land-use changes affected CATCHs
The BNM showed that climate and land-use changes could result in either increases or decreases in CATCHs across the 31 study lakes (Table 2). These results accounted for fish stocking and fishing effort (EFF), which both could have strong effects on CATCHs34,35,36 (Table 2). Based on the 75% one-tailed credible intervals (CIs) of BNM coefficients, the effects of a climate or land-use driver (one of air temperature (AT), precipitation (PRE), and agricultural land use (LUag) in this study) on lake-environmental factors (WT, WL, and primary productivity) were more consistent in directions (positive or negative) across lakes than the consequential changes in a lake-environmental factor on CATCHs across lakes. Specifically, four of the six BNM variable pairs between the climate land-use drivers and lake-environmental factors (brown arrows in Fig. 2; Table 2) were consistent in the directional relationships across at least half of the 31 study lakes: AT was positively related to WT in all 31 study lakes, but negatively related to WL in 17 lakes, PRE was positively related to WL in 29 lakes, and LUag was positively related to chlorophyll a (CHL), the measure of primary productivity in this study, in 16 lakes. In contrast, none of the 5 BNM variable pairs relating lake-environmental factors to each other or to CATCH (blue arrows in Fig. 2; Table 2) had a consistent directional relationship across the study lakes, although the closest was WT being negatively related to CHL in 15 lakes.
Changes in drivers associated with a 25% catch decrease
Our simulations showed that a 25% catch decrease (from the 1970–2014 medians) was associated with both colder and warmer AT across the 31 study lakes (Fig. 4a), and the effects of AT on CATCHs were mostly mediated though changes in WT (Fig. 4e, h) rather than WL (Fig. 4f) or CHL (Fig. 4g). For 8 of the 31 lakes, a simulated 25% catch decrease was associated with colder AT (i.e., a positive relationship), with medians of 0.9–3.6 °C colder than the observed 1970–2014 medians (Fig. 4a). For another eight lakes, however, a simulated 25% catch decrease was associated with warmer AT (i.e., a negative relationship), with medians of 0.8–1.7 °C warmer than the observed 1970–2014 medians. For these 16 lakes, the simulated relationship between AT and WT was consistently positive (Fig. 4b), whereas the simulated relationships between AT and WL (Fig. 4c) and between AT and CHL (Fig. 4d) could be either positive, negative, or mixed. Translating these simulated changes to effects on CATCHs revealed that the effects of WT, resulting from changes in AT, were important in 8 of these 16 lakes (i.e., leading to a >9.1% catch decrease in simulations; Fig. 4e), even though both colder and warmer WT could lead to a catch decrease. The effects of WL, resulting from changes in AT, on catch decrease were important in 2 of these 16 lakes (Fig. 4f), where warmer AT were associated with lower WL which, in turn, resulted in lower catches. The effects of CHL, resulting from changes in AT, on catch decrease were not important in any of these 16 lakes. For the remaining 15 lakes, a mixed relationship was revealed as a simulated 25% catch decrease was associated with both colder and warmer AT.
A simulated 25% catch decrease was associated with both higher and lower PRE across the study lakes (Fig. 5a), but these effects were mediated through changes in both WL (Fig. 5d, f) and CHL (Fig. 5e, f). For 10 lakes, a simulated 25% catch decrease was associated with lower PRE (i.e., a positive relationship), with medians of 15–71% lower than the observed 1970–2014 medians (Fig. 5a). For another six lakes, a simulated 25% catch decrease was associated with higher PRE (i.e., a negative relationship), with medians of 20–36% higher than the observed 1970–2014 medians. For these 16 lakes, the simulated relationship between PRE and WL was consistently positive (Fig. 5b), while the simulated relationship between PRE and CHL could be either positive, negative, or mixed (Fig. 5c). Translating these simulated changes to effects on CATCHs revealed that the effects of CHL were important in 7 of these 16 lakes (i.e., leading to a >13.4% catch decrease in simulations), but inconsistent relationships underlie this pattern: lower PRE was associated with both lower and higher CHL. The effects of WL, resulting from changes in PRE, on catch decrease were important only in 2 of these 16 lakes (Fig. 5d), where higher PRE increased WL. For the remaining 15 lakes, a mixed relationship was revealed as a simulated 25% catch decrease was associated with both lower and higher PRE.
Similarly, a simulated 25% catch decrease was associated with both increasing and decreasing LUag across the 31 study lakes (Fig. 6a), but effects of LUag on CATCHs were mostly mediated through changes in CHL (Fig. 6e, f) rather than through WL (Fig. 6d, f). For nine lakes, a simulated 25% catch decrease was associated with decreasing LUag (i.e., a positive relationship), with median decreases of 3.0–6.9% of catchment area from the observed 1970–2014 medians (Fig. 6a). In turn, these simulated decreases in LUag resulted in lower CHL for eight of these nine lakes, but a higher CHL in the other (Fig. 6c). For another 12 lakes, a simulated 25% catch decrease was associated with increasing LUag (i.e., a negative relationship), with median increases of 1.2–14.0% of catchment area from the observed 1970–2014 medians (Fig. 6a). However, the simulated effects of increasing LUag on CHL were more variable across lakes, some associated with higher CHL and some associated with lower CHL (Fig. 6c). Translating these simulated changes to effects on CATCHs revealed that the effects of CHL, resulting from changes in LUag, were important in all 21 lakes (i.e., leading to a >13.4% catch decrease), but once again the direction of the relationships varied across lakes, particularly when LUag increased. The effects of WL, resulting from changes in LUag, on catch decrease were unimportant in these 21 lakes. For the remaining 10 lakes, a mixed relationship was revealed as a simulated 25% catch decrease was associated with both lower and higher LUag.
Characteristics of lakes where CATCHs are vulnerable
Our results showed that access to clean water (as measured by the proportion of population in the catchment using drinking-water and sanitation services37) was positively correlated with the magnitude of changes in each of AT, PRE, and LUag that was associated with a 25% catch decrease across the study lakes (AT: r = 0.56, t-test p < 0.01, N = 31; PRE: r = 0.51, t-test p < 0.01, N = 31; LUag: r = 0.50, t-test p < 0.01, N = 31; Fig. 7a–c). This suggests that limited access to clean water is a characteristic for lakes where CATCHs are vulnerable to both climate and land-use changes, as relatively small changes (either increases or decreases) in AT, PRE, or LUag can cause a 25% catch decrease. Our results also showed that the magnitude of changes in LUag associated with a 25% catch decrease was negatively correlated with the shoreline development index (SDI), a measure of the circularity of lake surface and an indicator of littoral area relative to lake area24, across the study lakes (r = −0.39, t-test p = 0.03, N = 31; Fig. 7l). This suggests that lakes with larger littoral area (as indicated by a higher SDI) were more vulnerable because they required relatively small changes in LUag (either increases or decreases) to cause a 25% catch decrease. Across the study lakes, however, there was no significant correlation (i.e., t-test p > 0.05, N = 31) for all combinations between the magnitude of changes in each of AT, PRE, and LUag associated with a 25% catch decrease and shoreline population density or average depth (Fig. 7d–i), and between the magnitude of changes in each of AT and PRE associated with a 25% catch decrease and SDI (Fig. 7j, k).
Discussion
By using a Bayesian networks modeling approach to analyze time-series data for 31 lakes across five continents in the period 1970–2014, we found that climate and land-use changes could have both positive and negative effects on CATCHs. At one level, we found that effects of a climate or land-use driver (one of AT, PRE, and LUag in this study) on lake-environmental factors (WT, WL, and primary productivity) were relatively consistent in directions (e.g., warmer AT always increased WT). However, the effects of a changing lake-environmental factor (e.g., CHL) could have either positive or negative effects on CATCHs across lakes (Table 2).
One likely explanation for the lack of a consistent response across lakes is the abiotic and biotic diversity of lake ecosystems that could not be incorporated within our global model. For example, increases in WT can have both positive and negative effects on fish growth and recruitment38, but the direction of these effects on individual fish species usually depends upon the thermal tolerance of this species and the thermal environment of the lake27,39,40. Within a lake, as most fisheries are multi-species and multi-gear in nature, fishers are able to adapt, usually gradually, to changes in the composition of fish species6. There is a rich literature reporting how different fish species responded differently to lake-environmental changes that could be linked to changes in climate and land use9,41,42,43,44, especially in lakes where some species are close to the boundary of their current distributions40,45. However, in response to climate and land-use changes, lake environment21 may change at a very rapid pace so that native species cannot adapt, which, at an extreme, could create conditions for highly productive, introduced/exotic species to flourish and become dominant in CATCHs11,14,46. For lakes where the catch and effort could be subdivided into trophic levels or habitat guilds, future research could modify our existing modeling framework to predict catch at relevant trophic levels, for example, to evaluate whether a consistent catch response across lakes can be detected.
By assessing changes in climate and land-use drivers associated with a substantial, 25%, decrease in CATCHs across the 31 study lakes, we identified key processes that could underlie declines in CATCHs. Specifically, we found that changes in AT influence catches more through changes in WT than through changes in WL or primary productivity (as measured by CHL; Fig. 4h). Our BNM revealed strong positive relationships between AT and WT across all the 31 study lakes, which is consistent with predictions based on energy balance and findings in another global study21. Given robust projections for climate warming throughout this century47, our results suggest that projected increases in AT will result in increases in WT, but will not necessarily lead to widespread declines in CATCHs across lakes, as our simulations revealed that decreases in CATCHs were associated with warmer AT in only 7 of the 31 study lakes. One important caveat is that the largest AT increase in our model was 2.6 °C warmer than the 1970–2014 median. We caution against extrapolating our results should AT warm to even higher temperatures.
We found that changes in PRE could lead to substantial declines in CATCHs through changes in either WL or primary productivity (as measured by CHL; Fig. 5f). Across 29 of the 31 study lakes, our BNM suggested strong positive relationships between PRE and WL, which is consistent with water cycle and runoff dynamics. However, the lack of any consistent pattern of linkages between PRE and primary productivity revealed in our BNM exemplifies the diversity of lake systems. In theory, increased PRE can result in increases in primary productivity in a lake, directly through increasing inputs of allochthonous-derived nutrients from the catchment24 and indirectly through increasing WL that lead to the release of nutrients from inundated riparian land48. Nonetheless, depending on the timing, duration, and intensity of PRE, the increased PRE can also result in increases in sediment loads and resuspension, which can result in decreases in water clarity and primary productivity18. Based on current projections for this century, generally, future PRE may increase in the high-latitude (>40°) and near-equator (latitude <10°) regions, but decrease in mid-latitude regions47. As shown in Supplementary Data 2, these projections suggest that 21 of the 31 study lakes will have PRE increases, yet the scenarios under which these 21 lakes experienced decreases in CATCHs in our simulations included increased PRE (four lakes), reduced PRE (eight lakes), and mixed (nine lakes). While these projections suggest that 10 of the 31 study lakes will have PRE decreases (Supplementary Data 2), the scenarios under which these 10 lakes experienced decreases in CATCHs in our simulations also included increased PRE (two lakes), reduced PRE (two lakes), and mixed (six lakes). As a result, although projected changes in PRE will result in consistent directional changes in WL, it will not necessarily result in the same directional changes in primary production and CATCHs across lakes. Finally, although the projected changes in PRE across global change scenarios47 are generally within the range of our BNM inputs (i.e., from 63% lower to 51% higher than the 1970–2014 median), we caution against extrapolating our results should PRE change beyond this range.
While increases in LUag could affect lake ecosystems increasing water withdrawals and nutrient inputs, which could result in decreases in WL and increases in primary productivity2, we found that changes in LUag affected CATCHs more through changes in primary productivity (as measured by CHL) than through changes in WL (Fig. 6f). However, our BNM showed that increases in LUag could result in increases in primary productivity in 17 of the 31 study lakes, which suggests that in the remaining 14 study lakes, the positive relationship between nutrient inputs and LUag was decoupled. One plausible explanation for this decoupling is that the intensity of agriculture in a lake’s catchment could increase with little or no change in the area of agricultural land, such as through increases in fertilizer use49, livestock densities49, or cage culture50. Additionally, the area of LUag does not reflect the management efforts to control nutrient enrichment in recipient lakes, which is very common in developed countries2,43, but less so in developing countries.
Generally, LUag is projected to increase in developing countries but decrease in developed countries in this century51. As shown in Supplementary Data 2, 16 of the 31 study lakes are projected to have decreases in LUag and the scenarios under which these lakes experienced decreases in CATCHs in our simulations included increased LUag (eight lakes), reduced LUag (two lakes), and mixed (six lakes). Similarly, among 15 lakes that are projected to undergo increases in LUag, the scenarios under which these lakes experienced decreases in CATCHs in our simulations included increased LUag (four lakes), reduced LUag (seven lakes), and mixed (four lakes). Once again, our results suggest that projected changes in LUag will not necessarily result in the same directional changes in primary production and CATCHs across lakes and we caution against extrapolating our results should agricultural land-use change beyond the range of our BNM inputs (from an decrease of 13% to an increase of 11%, in terms of percent of catchment area, from the 1970–2014 median).
We identified low access to clean water (as measured by the proportion of population using drinking-water and sanitation services in the catchment) as one characteristic of lakes where CATCHs are vulnerable to changes in AT, PRE, and LUag (Figs. 7a–c and 8). Access to clean water can only be improved with substantial investments for water-use efficiency and water-quality protection37. Therefore, combining with the identified key processes that underlie changes in CATCHs (Figs. 4h, 5f, and 6f), these results suggest that the investments for water-use efficiency and water-quality protection can also make CATCHs less vulnerable to climate and land-use changes. Future research will be required to determine whether this correlation is causative; one potential mechanism that has support from previous studies is that investments in sanitation improve fish habitat2,9. One caveat is that lakes in regions with more access to clean water may also have stronger fishing regulations, which could also make CATCHs less vulnerable to climate and land-use changes by sustaining healthier fish stocks. We were unable to disentangle these effects in our analysis because none of the 31 study lakes has both high access to clean water and limited or weak fishing regulations.
Independent of access to clean water, our results suggest that climate and land-use changes can result in substantial decreases in CATCHs across lakes with very different socio-economic and hydrogeomorphological characteristics, such as shoreline population densities, depths, and littoral areas (Figs. 7d–k and 8). Although we identified a large littoral area (as indicated by SDI) as one characteristic for lakes where CATCHs are vulnerable to changes in LUag, the significant relationship was driven by two lakes with SDI >7 (Fig. 7l). Therefore, more research is needed to confirm this suggestion.
Throughout this study, we interpreted the results across the 31 study lakes collectively, with a focus on understanding effects of climate and land-use on CATCHs at a global scale (Figs. 3–7). We caution against interpreting our lake-specific results because the uncertainty around some predictions can be large, and it is difficult to discern whether this is a consequence of structural errors in our BNM or the uncertainty that arises from using data from so many sources (Supplementary Data 3). However, we suggest using our lake-specific predictions as priors for future lake-specific assessments, where quantitative models can be tailored to include important, lake-specific drivers that we were not able to include in our global model and data collected by consistent methods can be obtained. This is especially relevant to lakes where effects of climate or land-use change alone on CATCHs has not been as prevalent as effects of other anthropogenic stressors, such as pollution, invasive species, and overfishing; however, climate and land-use changes may exacerbate the negative effects of these stressors on CATCHs39.
In conclusion, although we were unable to identify consistent directional relationships between lake-environmental variables (e.g., WT, WL, CHL) and CATCH (Table 2; Figs. 4–6), correlations based on our simulations suggested an intriguing and potentially important relationship between access to clean water and vulnerability to a large reduction in CATCH in response to climate and land-use changes (Figs. 7 and 8). As an extension, our results suggest that CATCHs for lakes in developing countries in sub-Saharan Africa, Southeastern and Central Asia, and Central and South America are more vulnerable, which is consequential given that inland CATCHs are among the highest in the world in these regions and that the main purpose of fishing is for food rather than income6. To mitigate the threat of significant decreases in CATCHs and food security, our results imply that development strategies that include investments for clean water37 can also benefit lake CATCHs in the face of anthropogenic stressors (Fig. 8). The implications of this result made possible by analyzing time series of lakes across continents highlight possible synergies for policy makers aiming to achieve multiple United Nation Sustainable Development Goals (SDGs)52, including Zero Hunger (SDG 2), Clean Water and Sanitation (SDG 6), Climate Action (SDG 13), and Life Below Water (SDG 14), and Life on Land (SDG 15).
Methods
Choice of modeling approach
We chose to use a Bayesian networks modeling approach because it could minimize negative effects of data limitations on the statistical power of our analysis, by accounting for our understanding of multi-level, causal processes that could underlie changes in CATCHs in response to changes in climate and land use across lakes. A BNM could be developed to represent the hypothesized causal processes by expressing them as conditional probabilistic relationships between model variables, with which the estimation of every BNM coefficient took all model inputs derived from data into account20. For example, if we developed a simple BNM to represent that changes in AT resulted in changes in WT, which, in turn, resulted in changes in CATCH in a lake, the estimation of model coefficients for the relationship between AT and WT and for the relationship between WT and CATCH would both take model inputs for all variables (AT, WT, and CATCH) into account. Although the 31 study lakes were selected partly because of good data availability, there were still large within-lake differences in data availability among model variables (as shown in Supplementary Data 3). For example, we obtained 9, 16, and at least 32 years of data for CHL, WT, and all the other variables in Lake Chilwa, respectively. Therefore, the BNM’s capability of taking all model inputs into account for the estimation of every model coefficient was important to maximize the statistical power of our analysis.
Model development
To mathematically formulate our BNM based on our hypothesized causal processes (Fig. 2), we assumed that (1) each response variable in the BNM has a normal distribution, with a mean that can be expressed as a function of predictor variables based on the primary literature described below, and (2) annual time-series data are independent observations, such that the mean value of each response variable in 1 year is dependent upon the values of predictor variables in the same year, but independent from all of its mean values in the other years. For example, the conditional probability distribution of WT in our BNM was expressed as
where NORM(μ, σ) represents a normal distribution with a mean of μ and a standard deviation of σ, subscripted i indicates the ith lake, superscripted WT indicates that the parameter or BNM coefficient was associated with the response variable WT, and β represents a BNM coefficient. In Eq. (1), μWT was expressed as a linear function of AT based on the primary literature21 and was assumed to be dependent upon the observed value of AT in the same year, but independent from any μWT of the other years. In a similar manner, we give details for how we developed the conditional probability distributions of the other three BNM response variables—change in water level (ΔWL), CHL, and CATCH—in the following of this section.
The conditional probability distribution of ΔWL in our BNM was developed based on an empirical linear relationship between ΔWL and annual catchment runoff (RUNOFF)23, of which the latter could be expressed as a balance between PRE and evapotranspiration (ET)53. In a simple manner, these relationships could be expressed as
where α represents an empirical coefficient, PE is potential evaporation, LUun is undeveloped land use, and α1ET × PE × LUag and α2ET × PE × LUun represent ET over agricultural area and undeveloped area, respectively. In this study, we categorized catchment land use into three types: agricultural (which includes cropland, managed pasture, and rangeland), undeveloped (which includes forest, primary and secondary non-forest land, the lake itself, and other water and ice area), and urban. Equation (3) did not include urban land use because urban water use is mostly non-consumptive and returns to the catchment54. By combining Eqs. (2) and (3) and re-arranging α coefficients, the conditional probability distribution of ΔWL in our BNM was expressed as
where each β coefficient can be expressed as a combination of α coefficients in Eqs. (2) and (3). We only included LUag in Eq. (4) because in each of these 31 study lakes, LUag + LUun in the catchment was almost a constant, which means that LUun could be replaced with a constant minus LUag, as the increase in agricultural area mostly resulted from the decrease in undeveloped area, or vice versa, in the study period.
The conditional probability distribution of CHL in our BNM was developed based on empirical log–log relationships between CHL and total phosphorus24 and between CHL and WT25. Because total phosphorus data were only available for a few of our study lakes, we modeled the total phosphorus in lakes as a function of PRE26, LUag26, and ΔWL29. This led to a conditional probabilistic distribution for CHL expressed as
where μWT and μΔWL are from Eqs. (1) and (4), respectively.
Finally, the conditional probability distribution of CATCH was developed based on (1) a theoretical relationship between CATCH and fish biomass (B)34, (2) a hypothesized empirical relationship between fishing catchability (Q) and EFF and B34, and (3) a hypothesized empirical relationship between B and WT27,28, ΔWL29,30, and CHL31,32 and number of fish stocked (ST)35,36. In a simple manner, these relationships could be expressed as
By combining Eqs. (6)–(8) and re-arranging α coefficients, we developed the conditional probabilistic distribution for CATCH expressed as
where μWT, μΔWL, and μCHL are from Eqs. (1), (4), and (5), respectively. As described in the Supplementary Methods, we did not estimate β4,iCATCH for 23 lakes where stocking effects on CATCHs were not sufficiently important in the study period.
The derivations and data sources of model inputs, including climate and land-use drivers (AT, PRE, and LUag), lake-environmental factors (WT, WL, and CHL), CATCH, ST, and EFF are given in the Supplementary Methods.
Prior distributions
We followed a previously used procedure20 to derive prior distributions of BNM coefficients. For example, to derive the prior distribution of \(\beta _{i}^{{\mathrm{WT}}}\), we first expressed the function of \(\mu _{i}^{{\mathrm{WT}}}\) in Eq. (1) as 31 linear models (i.e., one for each study lake) in a form
where ε is the residual error. Then we derive the least-squares estimates for the coefficients of each of these 31 linear models based on model inputs derived from data for WTi and ATi in the same year. In theory, the least-squares estimates for the coefficients of each of these 31 linear models have a multivariate normal (MVN) distribution because they could be expressed as linear combinations of WTi, which was assumed to have a normal distribution as shown in Eq. (1). Finally, we used the MVN distribution for the least-squares estimates of the linear model coefficients as the prior distribution of each of the 31 sets of βiWT, but the covariance matrix of the MVN distribution was set to be proportional to its un-scaled, least-squares estimates, with a proportional constant (i.e., the hyperparameter) having a noninformative (hyperprior) distribution20. We repeated this procedure to derive prior distributions for βiΔWL, βiCHL, and βiCATCH. The prior distributions of these BNM coefficients were always developed on a lake-by-lake basis because for each of the 31 study lakes, we were able to obtain data to derive model inputs for at least 9 years for all BNM variables (refer to Supplementary Data 3 for data sources and availability). Lastly, for nuisance parameters σWT, σΔWL, σCHL, and σCATCH in Eqs. (1), (4), (5), and (9), respectively, we set each of them to have a noninformative prior distribution.
Coefficient estimation
The posterior distributions of our BNM coefficients were developed based on pooled information across the 31 study lakes. Our BNM was structured in a way to have the transferability of information across the lakes informed by data. Specifically, in the derivation of posterior distributions of our BNM coefficients, the relative importance of lake-specific information increases with lake-specific sample size and across-lake difference. If a lake was very different from all the other lakes, for example, the relative importance of its lake-specific information would be much higher than across-lake information in the derivation of posterior distributions of lake-specific BNM coefficients.
Computationally, we derived empirical posterior distributions for all BNM coefficients by using a Gibbs sampling method to run Markov chain Monte Carlo (MCMC) simulations55. We ran three random-starting MCMC chains by implementing the program JAGS56 and the package runjags57 in R58. After discarding 20,000 iterations for burn-in and adaptation, we considered that the convergence of three MCMC chains was achieved at 50,000 interactions as autocorrelations were close to 0 and Gelman and Rubin’s convergence diagnostics59 were <1.005 for all coefficients. Our empirical posterior distribution of each BNM coefficient was based on 50,000 samples from each converged MCMC chain.
Effects between variable pairs
As shown in Fig. 2, there were 13 pairs of predictor and response variables in our BNM. For each of these 13 variable pairs, we categorized the effects of predictor variable on response variable as positive, negative, and mixed in each lake based on the posterior distribution of the associated BNM coefficient, which we used as a proxy of effect strength because it represents how much the response variable would change in response to one unit change in the predictor variable. For example, we categorized the effects of AT on WT in lake i based on the posterior distribution of β1,iWT, which represents how much of WT would increase in response to one unit change of AT. We categorized effects between a variable pair as positive and negative based on the 75% CI of the associated BNM coefficient. We categorized effects between a variable pair as mixed when both positive and negative 75% CIs of the associated BNM coefficients included 0, which, statistically, also means that its 50% CI included 0.
Changes in drivers associated with a 25% catch decrease
We implemented the BNM and used a Monte Carlo simulation method to empirically derive distributions of climate (AT and PRE) and land-use (LUag) drivers associated with a 25% decrease in CATCH from its 1970–2014 median (i.e., a 25% catch decrease) in each of the 31 study lakes. We used a 25% catch decrease as our simulation target because it is close to the maximum value of standard errors for the ratios of CATCH to its median, which ranged from 2.1% to 25.7% across the study lakes in the study period.
Monte Carlo simulation
Our Monte Carlo simulation was a three-step process. The first step was to randomly sample a set of BNM coefficients (i.e., βWT, βΔWL, βCHL, and βCATCH) from empirical posterior distributions by implementing the package rv60 in R. Then, we calculated predicted medians of WT, ΔWL, CHL, and CATCH (denoted as μ0WT, μ0ΔWL, μ0CHL, and μ0CATCH, respectively) using the set of BNM coefficients and the 1970–2014 medians of all BNM inputs.
The second step was to generate a set of BNM inputs from probability distributions based on lake-by-lake data by implementing random number generators in R. We assumed that each of AT, PRE, and LUag has a normal distribution. PE was derived empirically based on randomly sampled AT and the assumption that temperature change is uniform throughout the year (e.g., if randomly sampled AT was 1 °C higher than its 1970–2014 median, we assumed that AT in every month was 1 °C higher than its 1970–2014 median).
The third step was to calculate predicted values (i.e., μWT, μΔWL, μCHL, and μCATCH) using randomly sampled BNM coefficients, randomly sampled values of one climate or land-use drivers, and 1970–2014 medians of the other climate and/or land-use variables not being evaluated. For example, to investigate effects of AT on CATCH, we calculated BNM predicted values using BNM coefficients randomly sampled from empirical posterior distributions, inputs of AT randomly sampled from normal distributions, inputs of PE derived based on random samples of AT, and 1970–2014 medians of PRE and LUag.
We kept the set of BNM coefficients, inputs, and predicted values that led to a ratio of predicted CATCH to predicted median CATCH, which was calculated as [exp(μCATCH − μ0CATCH)], between 0.74 and 0.76, and assumed they were associated with a 25% catch decrease. We repeated the Monte Carlo simulation process until we obtained 10,000 samples associated with a 25% catch decrease for each lake to derive empirical probability distributions.
Assessment of climate and land-use effects
We assessed how climate and land-use drivers (i.e., AT, PRE, and LUag) could lead to a 25% catch decrease by analyzing empirical probability distributions derived from samples obtained in our Monte Carlo simulations.
To assess effects of AT on CATCH in each of the 31 study lakes, we analyzed empirical probability distributions associated with a 25% catch decrease for changes in AT, predicted effects of AT on WT, WL, and CHL, and predicted effects of WT, WL, and CHL on CATCH. We used predicted changes in WT, WL, and CHL driven by AT to quantify effects of AT on WT, WL, and CHL, respectively. Following the methods used by the Intergovernmental Panel on Climate Change (IPCC)47, we calculated predicted changes as an actual difference from the 1970–2014 medians for AT, WT, and WL and as a percent difference from the 1970–2014 median for CHL. We used predicted changes in CATCH driven by WT, WL, and CHL to quantify effects of WT, WL, and CHL on CATCH, respectively. The predicted changes in CATCH driven by WT, WL, and CHL were calculated as percent differences from the 1970–2014 medians based on Eq. (9). For example, we calculated predicted effects of WT on CATCH as
Similar to how we summarized BNM coefficients, we also categorized relationships between AT and CATCH and between AT and each of WT, WL, and CHL as positive, negative, and mixed based on 75% CIs of their changes associated with a 25% catch decrease in each lake. Further, we considered effects of WT, WL, or CHL on CATCH to be important in each lake if its predicted effects could lead to a >9.1% catch decrease based on 75% CI. The cutoff value 9.1% was calculated as (1–0.751/3) × 100%, based on the assumption that WT, WL, and CHL contributed equally to a 25% catch decrease.
With two changes, we followed the same method used to assess AT effects on CATCH to assess effects of PRE and effects of LUag on CATCH. First, following the IPCC methods for calculating projected global distributions of changes in PRE and land use, we calculated predicted changes as a percent difference from the 1970–2014 median for PRE and as an actual difference from the 1970–2014 median for LUag. Second, we did not analyze changes in WT and effects of WT on CATCH in both assessments, because there was no hypothesized linkage between PRE and WT and between LUag and WT (Fig. 2). Consequently, since effects of WT on CATCH were not assessed, we considered effects of WL or CHL on CATCH to be important in each lake if its predicted effects could lead to a >13.4% catch decrease based on 75% CI. The cutoff value 13.4% was calculated as (1–0.751/2) × 100%, based on the assumption that WL and CHL contributed equally to a 25% catch decrease.
Characteristics of lakes where CATCHs are vulnerable
We define vulnerability of a lake as the extent to which the focal unit (e.g., CATCH) will be adversely affected by environmental changes61. In this study, we used the magnitude of change for each of AT, PRE, and LUag associated with a 25% catch decrease to index the vulnerability of a lake to a 25% catch decrease owing to climate and land-use changes. For example, we considered a hypothetical lake A to be more vulnerable than another hypothetical lake B if the magnitude of change for each of AT, WL, and CHL associated with a 25% catch decrease was smaller in lake A than lake B.
We investigated whether the vulnerability of a lake to a 25% catch decrease corresponded to any of the two socio-economic characteristics associated with the catchment: access to clean water and shoreline population density; and any of the two hydrogeomorphological characteristics of the lake: average depth and SDI. The access to clean water was indicated by the proportion of population using drinking-water and sanitation services in the catchment37. The shoreline population density was the population density within 10 km of a lake’s shoreline. SDI is a measure of circularity of the lake surface24, which is defined as
where SL is shoreline length and Alake is lake area. A larger SDI indicates that the lake surface is less circular and may have a larger littoral area relative to lake area. The derivations and values of these socio-economic and hydrogeomorphological characteristics are given in the Supplementary Methods.
We conducted a correlation analysis to evaluate whether the relationship between each of the 4 socio-economic and hydrogeomorphological characteristics and the magnitude of change for each of AT, PRE, and LUag associated with a 25% catch decrease was significant at p = 0.05 level (t test, N = 31). To quantify the magnitude of change for each of AT, WL, and CHL associated with a 25% catch decrease, we used the predicted median of absolute change associated with a 25% catch decrease, which was calculated from empirical probability distributions derived from samples obtained in our Monte Carlo simulations.
Reporting summary
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Data availability
Data used to derive model inputs for variables associated with lake environment, fish catch, fish stocking, and fishing effort (i.e., WT, ΔWL, CHL, CATCH, ST, and EFF) are either publicly available or available upon requests to corresponding authorities, as given in Supplementary Data 3. Data used to derive model inputs for variables associated with climate and land use (i.e., AT, PRE, PE, and LUag) are from publicly available global databases, as described the Supplementary Methods. The source data underlying Figs. 4a–g, 5a–e, 6a–e, 7, and 8 are provided as a Source Data file.
Code availability
References
La Notte, A. et al. Ecosystem services classification: a systems ecology perspective of the cascade framework. Ecol. Indic. 74, 392–402 (2017).
Beeton, A. M. Large freshwater lakes: present state, trends, and future. Environ. Conserv 29, 21–38 (2002).
Carpenter, S. R., Stanley, E. H. & Vander Zanden, M. J. State of the world’s freshwater ecosystems: physical, chemical, and biological changes. Annu. Rev. Environ. Resour. 36, 75–99 (2011).
Allan, J. D. Landscapes and riverscapes: the influence of land use on stream ecosystems. Annu. Rev. Ecol. Evol. Syst. 35, 257–284 (2004).
Magnuson, J. J. et al. Potential effects of climate changes on aquatic systems: Laurentian Great Lakes and Precambrian Shield region. Hydrol. Process. 11, 825–871 (1997).
Welcomme, R. L. et al. Inland capture fisheries. Philos. Trans. R. Soc. Ser. B 365, 2881–2896 (2010).
Venard, J. A. & Scarnecchia, D. L. Seasonally dependent movement of lake trout between two northern Idaho lakes. N. Am. J. Fish. Manag. 25, 635–639 (2005).
Araújo, C. V. M. et al. Habitat fragmentation caused by contaminants: atrazine as a chemical barrier isolating fish populations. Chemosphere 193, 24–31 (2018).
Ludsin, S. A., Kershner, M. W., Blocksom, K. A., Knight, R. L. & Stein, R. A. Life after death in Lake Erie: nutrient controls drive fish species richness, rehabilitation. Ecol. Appl. 11, 731–746 (2001).
Ostrovsky, I., Zohary, T., Shapiro, J., Snovsky, G. & Markel, D. in Lake Kinneret: Ecology and Management (eds Zohary, T., Sukenik, A., Berman, T., & Nishri, A.) 635–653 (Springer, 2014).
Britton, J. R. et al. From introduction to fishery dominance: the initial impacts of the invasive carp Cyprinus carpio in Lake Naivasha, Kenya, 1999 to 2006. J. Fish. Biol. 71, 239–257 (2007).
Hickley, P. et al. Habitat degradation and subsequent fishery collapse in Lakes Naivasha and Baringo, Kenya. Ecohydrol. Hydrobiol. 4, 503–517 (2004).
Kangur, K., Park, Y.-S., Kangur, A., Kangur, P. & Lek, S. Patterning long-term changes of fish community in large shallow Lake Peipsi. Ecol. Model. 203, 34–44 (2007).
van Zwieten, P. A. M. et al. The Nile perch invasion in Lake Victoria: cause or consequence of the haplochromine decline? Can. J. Fish. Aquat. Sci. 73, 622–643 (2015).
Thorpe, A. & van Anrooy, R. Inland Fisheries Livelihoods in Central Asia: Policy Interventions and Opportunities. (FAO, 2009).
Lynch, A. J. et al. Inland fisheries—invisible but integral to the UN Sustainable Development Agenda for ending poverty by 2030. Glob. Environ. Change 47, 167–173 (2017).
Keatley, B. E., Bennett, E. M., MacDonald, G. K., Taranu, Z. E. & Gregory-Eaves, I. Land-use legacies are important determinants of lake eutrophication in the anthropocene. PLoS ONE 6, e15913 (2011).
McCullough, I. M., Cheruvelil, K. S., Collins, S. M. & Soranno, P. A. Geographic patterns of the climate sensitivity of lakes. Ecol. Appl. 29, e01836 (2019).
Messager, M. L., Lehner, B., Grill, G., Nedeva, I. & Schmitt, O. Estimating the volume and age of water stored in global lakes using a geo-statistical approach. Nat. Commun. 7, 13603 (2016).
Qian, S. S. & Miltner, R. J. A continuous variable Bayesian networks model for water quality modeling: a case study of setting nitrogen criterion for small rivers and streams in Ohio, USA. Environ. Model. Softw. 69, 14–22 (2015).
O’Reilly, C. M. et al. Rapid and highly variable warming of lake surface waters around the globe. Geophys. Res. Lett. 42, 773–710,781 (2015).
Boughton, W. The Australian water balance model. Environ. Model. Softw. 19, 943–956 (2004).
Mason, I., Guzkowska, M., Rapley, C. & Street-Perrott, F. The response of lake levels and areas to climatic change. Clim. Change 27, 161–197 (1994).
Wetzel, R. G. Limnology: Lake and River Ecosystems (Academic Press, 2001).
Woelmer, W. M. et al. Assessing the influence of watershed characteristics on chlorophyll a in waterbodies at global and regional scales. Inland Waters 6, 379–392 (2016).
Soranno, P. A., Hubler, S. L., Carpenter, S. R. & Lathrop, R. C. Phosphorus loads to surface waters: a simple model to account for spatial pattern of land use. Ecol. Appl. 6, 865–878 (1996).
Kao, Y.-C., Madenjian, C. P., Bunnell, D. B., Lofgren, B. M. & Perroud, M. Potential effects of climate change on the growth of fishes from different thermal guilds in Lakes Michigan and Huron. J. Gt. Lakes Res. 41, 423–435 (2015).
Kao, Y.-C., Madenjian, C. P., Bunnell, D. B., Lofgren, B. M. & Perroud, M. Temperature effects induced by climate change on the growth and consumption by salmonines in Lakes Michigan and Huron. Environ. Biol. Fishes 98, 1089–1104 (2015).
Kolding, J. & van Zwieten, P. A. M. Relative lake level fluctuations and their influence on productivity and resilience in tropical lakes and reservoirs. Fish. Res. 115, 99–109 (2012).
Gownaris, N. J. et al. Water level fluctuations and the ecosystem functioning of lakes. J. Gt. Lakes Res. 44, 1154–1163 (2018).
Deines, A. M., Bunnell, D. B., Rogers, M. W., Beard, T. D. & Taylor, W. W. A review of the global relationship among freshwater fish, autotrophic activity, and regional climate. Rev. Fish. Biol. Fish. 25, 323–336 (2015).
Deines, A. M. et al. The contribution of lakes to global inland fisheries harvest. Front. Ecol. Environ. 15, 293–298 (2017).
Wang, Y. et al. Can water level management, stock enhancement, and fishery restriction offset negative effects of hydrological changes on the four major Chinese carps in China’s largest freshwater lake? Ecol. Model. 403, 1–10 (2019).
Arreguín-Sánchez, F. Catchability: a key parameter for fish stock assessment. Rev. Fish. Biol. Fish. 6, 221–242 (1996).
Gerdeaux, D. The recent restoration of the whitefish fisheries in Lake Geneva: the roles of stocking, reoligotrophication, and climate change. Ann. Zool. Fenn. 41, 181–189 (2004).
Kao, Y.-C., Rogers, M. W. & Bunnell, D. B. Evaluating stocking efficacy in an ecosystem undergoing oligotrophication. Ecosystems 21, 600–618 (2018).
United Nations. Sustainable Development Goal 6 Synthesis Report 2018 on Water and Sanitation (United Nations, 2018).
Farmer, T. M., Marschall, E. A., Dabrowski, K. & Ludsin, S. A. Short winters threaten temperate fish populations. Nat. Commun. 6, 7724 (2015).
Collingsworth, P. D. et al. Climate change as a long-term stressor for the fisheries of the Laurentian Great Lakes of North America. Rev. Fish. Biol. Fish. 27, 363–391 (2017).
Jeppesen, E. et al. Impacts of climate warming on the long-term dynamics of key fish species in 24 European lakes. Hydrobiologia 694, 1–39 (2012).
Kangur, K. et al. Long-term effects of extreme weather events and eutrophication on the fish community of shallow Lake Peipsi (Estonia/Russia). J. Limnol. 72, 376–387 (2013).
Ostrovsky, I. et al. in Climatic Change and Global Warming of Inland Waters (eds Goldman, C. R., Kumagai, M., & Robarts, R. D.) 271–293 (Wiley, 2012).
Jeppesen, E. et al. Lake responses to reduced nutrient loading—an analysis of contemporary long-term data from 35 case studies. Freshwat. Biol. 50, 1747–1771 (2005).
Weiperth, A. et al. Effect of water level fluctuations on fishery and anglers’ catch data of economically utilised fish species of Lake Balaton between 1901 and 2011. Appl. Ecol. Environ. Res. 12, 221–249 (2014).
Alofs, K. M., Jackson, D. A. & Lester, N. P. Ontario freshwater fishes demonstrate differing range-boundary shifts in a warming climate. Divers. Distrib. 20, 123–136 (2014).
Moncayo-Estrada, R., Lyons, J., Escalera-Gallardo, C. & Lind, O. T. Long-term change in the biotic integrity of a shallow tropical lake: a decadal analysis of the Lake Chapala fish community. Lake Reserv. Manag. 28, 92–104 (2012).
Pachauri, R. K. et al. Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC, 2014).
Gownaris, N. J. et al. Fisheries and water level fluctuations in the world’s largest desert lake. Ecohydrology 10, e1769 (2017).
Schindler, D. W., Hecky, R. E. & McCullough, G. K. The rapid eutrophication of Lake Winnipeg: greening under global change. J. Gt. Lakes Res. 38, 6–13 (2012).
Avadí, A. et al. Comparative environmental performance of artisanal and commercial feed use in Peruvian freshwater aquaculture. Aquaculture 435, 52–66 (2015).
Hurtt, G. C. et al. Harmonization of land-use scenarios for the period 1500–2100: 600 years of global gridded annual land-use transitions, wood harvest, and resulting secondary lands. Clim. Change 109, 117–161 (2011).
United Nations. Transforming our World: the 2030 Agenda for Sustainable Development (United Nations, 2015).
Berezovskaya, S., Yang, D. & Hinzman, L. Long-term annual water balance analysis of the Lena River. Glob. Planet. Change 48, 84–95 (2005).
Gleick, P. H. Water use. Annu. Rev. Environ. Resour. 28, 275–314 (2003).
Gelfand, A. E. & Smith, A. F. M. Sampling-based approaches to calculating marginal densities. J. Am. Stat. Assoc. 85, 398–409 (1990).
Plummer, M. JAGS: a program for analysis of Bayesian graphical models using Gibbs sampling. In Proc. 3rd International Workshop on Distributed Statistical Computing (DSC 2003) (Vienna, 2003)
Denwood, M. J. runjags: an R package providing interface utilities, model templates, parallel computing methods and additional distributions for MCMC models in JAGS. J. Stat. Softw. 71, 1–25 (2016).
R Core Team. R: A Language and Environment for Statistical Computing (R Foundation for Statistical Computing, 2017).
Gelman, A. & Rubin, D. B. Inference from iterative simulation using multiple sequences. Stat. Sci. 7, 457–472 (1992).
Kerman, J. & Gelman, A. Manipulating and summarizing posterior simulations using random variable objects. Stat. Comput. 17, 235–244 (2007).
Birkmann, J. et al. Scenarios for vulnerability: opportunities and constraints in the context of climate change and disaster risk. Clim. Change 133, 53–68 (2015).
South, A. rworldmap: a new R package for mapping global data. R J. 3, 35–43 (2011).
Acknowledgements
This research was funded by the US Geological Survey National Climate Adaptation Science Center. We thank help from A. Sakas for data compilation and email communication at the beginning of this project. We thank E. Politi for global database support and C. Paukert for comments on an earlier draft of this manuscript. Personal funding supports, data providers, and data sources are acknowledged in Supplementary Note. Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the US Government.
Author information
Authors and Affiliations
Contributions
Y.-C.K. led the work, carried out the study with help from M.W.R., D.B.B., and I.G.C., analyzed data with help from S.S.Q., M.W.R., D.B.B., and I.G.C., and wrote the initial draft of this manuscript with help from M.W.R. and D.B.B. The study was initiated by T.D.B. and initially designed by M.W.R. and D.B.B. O.A., T.D.B., A.B., J.R.B., R.C.-C., N.J.G, J.R.J., K.K., J.K., A.A.L., A.J.L., N.M.-S., R.M.-E., F.J.N., I.O., L.G.R., A.L.E.S., Y.S., H.S-M., A.T., P.A.M.Z., P.V., Y.W., A.W., O.L.F.W., and J.D.Y. contribute to obtain and compile data used in this study and provided inputs to the analyses and manuscript. Sixth through thirty-first authors contributed equally to this study and are listed alphabetically.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Peer review information Nature Communications thanks Laura Uusitalo and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Kao, YC., Rogers, M.W., Bunnell, D.B. et al. Effects of climate and land-use changes on fish catches across lakes at a global scale. Nat Commun 11, 2526 (2020). https://doi.org/10.1038/s41467-020-14624-2
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467-020-14624-2
This article is cited by
-
Reservoir ecosystems support large pools of fish biomass
Scientific Reports (2024)
-
Differential expression of miRNAs and mRNAs in the livers of largemouth bass Micropterus salmoides under heat stress
Journal of Oceanology and Limnology (2024)
-
W-FENet: Wavelet-based Fourier-Enhanced Network Model Decomposition for Multivariate Long-Term Time-Series Forecasting
Neural Processing Letters (2024)
-
Heat stress induced hepatocyte apoptosis in largemouth bass Micropterus salmoides via IRE1α/TRAF2/ASK1/JNK pathway
Journal of Oceanology and Limnology (2024)
-
Exploring vulnerabilities of inland fisheries in Indian context with special reference to climate change and their mitigation and adaptation: a review
International Journal of Biometeorology (2023)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.