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The knowledge of tropical palaeoclimates is crucial for understanding global climate change, because it is a test bench for general circulation models that are ultimately used to predict future global warming. A longstanding issue concerning the last glacial maximum in the tropics is the discrepancy between the decrease in sea-surface temperatures reconstructed from marine proxies and the high-elevation decrease in land temperatures estimated from indicators of treeline elevation. In this study, an improved inverse vegetation modeling approach is used to quantitatively reconstruct palaeoclimate and to estimate the effects of different factors (temperature, precipitation, and atmospheric CO 2 concentration) on changes in treeline elevation based on a set of pollen data covering an altitudinal range from 100 to 3,140 m above sea level in Africa. We show that lowering of the African treeline during the last glacial maximum was primarily triggered by regional drying, especially at upper elevations, and was amplified by decreases in atmospheric CO 2 concentration and perhaps temperature. This contrasts with scenarios for the Holocene and future climates, in which the increase in treeline elevation will be dominated by temperature. Our results suggest that previous temperature changes inferred from tropical treeline shifts may have been overestimated for low-CO 2 glacial periods, because the limiting factors that control changes in treeline elevation differ between glacial and interglacial periods.

ABSTRACT Aim  To document the patterns of fish species richness and their possible causes in China's lakes at regional and national scales. Location  Lakes across China. Methods  We compiled data of fish species richness, limnological characteristics and climatic variables for 109 lakes across five regions of China: East region, Northeast region, Southwest region, North‐Northwest region, and the Tibetan Plateau. Correlation analyses, regression models and a general linear model were used to explore the patterns of fish species richness. Results  At the national scale, lake altitude, energy availability (potential evapotranspiration, PET) and lake area explained 79.6% of the total variation of the lake fish species richness. The determinants of the fish richness pattern varied among physiographic regions. Lake area was the strongest predictor of fish species richness in the East and Southwest lakes, accounting for 22.2% and 82.9% of the variation, respectively. Annual PET explained 68.7% of the variation of fish richness in the Northeast lakes. Maximum depth, mineralization degree, and lake area explained 45.5% of the fish variation in the lakes of the North‐Northwest region. On the Tibetan Plateau, lake altitude was the first predictor variable, interpreting 32.2% of the variation. Main conclusions  Lake altitude was the most important factor explaining the variation of fish species richness across China's lakes, and accounted for 74.5% of the variation. This may stem in part from the fact that the lakes investigated in our study span the largest altitudinal range anywhere in the world. The effects of the lake altitude on fish species richness can be separated into direct and indirect aspects due to its collinearity with PET. We also found that the fish diversity and its determinants were scale‐dependent. Fish species richness was probably energy‐determined in the cold region, while it was best predicted by the lake area in the relatively geologically old region. The independent variables we used only explained a small fraction of the variations in the lake fish species richness in East China and the Tibetan Plateau, which may be due to the effects of human activity and historical events, respectively.

Abstract Digital leaf physiognomy (DLP) is considered as one of the most promising methods for estimating past climate. However, current models built using the DLP data set still lack precision, especially for mean annual precipitation (MAP). To improve predictive power, we developed five machine learning (ML) models for mean annual temperature (MAT) and MAP respectively, and then tested the precision of these models and some of their averaging compared with that obtained from other models. The precision of all models was assessed using a repeated stratified 10‐fold cross‐validation. For MAT, three combinations of models ( R 2 = .77) presented moderate improvements in precision over the multiple linear regression (MLR) model ( R 2 = .68). For log e (MAP), the averaging of the support vector machine (SVM) and boosting models improved the R 2 from .19 to .63 compared with that of the MLR model. For MAP, the R 2 of this model combination was 0.49, which was much better than that of the artificial neural network (ANN) model ( R 2 = .21). Even the bagging model, which had the lowest R 2 (.37) for log e (MAP), demonstrated better precision ( R 2 = .27) for MAP. Our palaeoclimate estimates for nine fossil floras were also more accurate, because they were in better agreement with independent paleoclimate evidence. Our study confirms that our ML models and their averaging can improve paleoclimatic reconstructions, providing a better understanding of the relationship between climate and leaf physiognomy.

Paleobotanists have long built leaf climate models based on site mean of leaf physiognomic characteristics of woody dicotyledons species (WDS) for estimating past climate. To explore the potential of the order Ericales in estimating paleoclimate, we developed two linear models for each climatic factor. One is based on WDS, and the other is based on both WDS and leaf physiognomic characters of the order Ericales (WDS-E). We found that, compared with WDS models, WDS-E models improved greatly in mean annual precipitation (MAP), growing season precipitation (GSP) and mean annual range in temperature (MART). When the minimum species number of the order Ericales is three per site, the WDS-E models improved the r2 from 0.64 to 0.78 for MART, from 0.23 to 0.61 for ln(MAP), and from 0.37 to 0.64 for ln(GSP) compared with the WDS models. For mean annual temperature (MAT), the WDS-E model (r2 = 0.86) also exhibited a moderate improvement in precision over the WDS model (r2 = 0.82). This study demonstrates that other patterns, such as those of the order Ericales, can contribute additional information towards building more precise paleoclimate models.

Abstract This study investigated seasonal patterns in stoichiometric ratios, nutrient resorption characteristics, and nutrient use strategies of dominant tree species at three successional stages in subtropical China, which have not been fully understood. Fresh leaf and leaf litterfall samples were collected in growing and nongrowing seasons for determining the concentrations of carbon (C), nitrogen (N), and phosphorus (P). Then, stoichiometric ratios (i.e., C:N, C:P, N:P, and C:N:P) and resorption parameters were calculated. Our results found that there was no consistent variation in leaf C:N and C:P ratios among different species. However, leaf N:P ratios in late‐successional species became significantly higher, indicating that P limitation increases during successional development. Due to the P limitation in this study area, P resorption efficiency and proficiency were higher than corresponding N resorption parameters. Dominant tree species at early‐successional stage adopted “conservative consumption” nutrient use strategy, whereas the species at late‐successional stage inclined to adopt “resource spending” strategy.

Dynamic global vegetation models (DGVMs) typically track the material and energy cycles in ecosystems with finite plant functional types (PFTs). Increasingly, the community ecology and modelling studies recognize that current PFT scheme is not sufficient for simulating ecological processes. Recent advances in the study of plant functional traits (FTs) in community ecology provide a novel and feasible approach for the improvement of PFT-based DGVMs. This paper reviews the development of current DGVMs over recent decades. After characterizing the advantages and disadvantages of the PFT-based scheme, it summarizes trait-based theories and discusses the possibility of incorporating FTs into DGVMs. More importantly, this paper summarizes three strategies for constructing next-generation DGVMs with FTs. Finally, the method’s limitations, current challenges and future research directions for FT theory are discussed for FT theory. We strongly recommend the inclusion of several FTs, namely specific leaf area (SLA), leaf nitrogen content (LNC), carbon isotope composition of leaves (Leaf δ 13 C), the ratio between leaf-internal and ambient mole fractions of CO 2 (Leaf C i /C a ), seed mass and plant height. These are identified as the most important in constructing DGVMs based on FTs, which are also recognized as important ecological strategies for plants. The integration of FTs into dynamic vegetation models is a critical step towards improving the results of DGVM simulations; communication and cooperation among ecologists and modellers is equally important for the development of the next generation of DGVMs.

Abstract Forest insects are major disturbances that induce tree mortality in eastern coniferous (or fir‐spruce) forests in eastern North America. The spruce budworm ( SBW ) ( Choristoneura fumiferana [Clemens]) is the most devastating insect causing tree mortality. However, the relative importance of insect‐caused mortality versus tree mortality caused by other agents and how this relationship will change with climate change is not known. Based on permanent sample plots across eastern Canada, we combined a logistic model with a negative model to estimate tree mortality. The results showed that tree mortality increased mainly due to forest insects. The mean difference in annual tree mortality between plots disturbed by insects and those without insect disturbance was 0.0680 per year ( P  <   0.0001, T ‐test), and the carbon sink loss was about 2.87t C ha −1  year −1 larger than in natural forests. We also found that annual tree mortality increased significantly with the annual climate moisture index ( CMI ) and decreased significantly with annual minimum temperature ( T min ), annual mean temperature ( T mean ) and the number of degree days below 0°C ( DD 0), which was inconsistent with previous studies (Adams et al. ; van Mantgem et al. ; Allen et al. ). Furthermore, the results for the trends in the magnitude of forest insect outbreaks were consistent with those of climate factors for annual tree mortality. Our results demonstrate that forest insects are the dominant cause of the tree mortality in eastern Canada but that tree mortality induced by insect outbreaks will decrease in eastern Canada under warming climate.

Paleobotanists have long built leaf climate models based on site mean of leaf physiognomic characteristics of woody dicotyledons species (WDS) for estimating past climate. To explore the potential of the order Ericales in estimating paleoclimate, we developed two linear models for each climatic factor. One is based on WDS, and the other is based on both WDS and leaf physiognomic characters of the order Ericales (WDS-E). We found that, compared with WDS models, WDS-E models improved greatly in mean annual precipitation (MAP), growing season precipitation (GSP) and mean annual range in temperature (MART). When the minimum species number of the order Ericales is three per site, the WDS-E models improved the r2 from 0.64 to 0.78 for MART, from 0.23 to 0.61 for ln(MAP), and from 0.37 to 0.64 for ln(GSP) compared with the WDS models. For mean annual temperature (MAT), the WDS-E model (r2 = 0.86) also exhibited a moderate improvement in precision over the WDS model (r2 = 0.82). This study demonstrates that other patterns, such as those of the order Ericales, can contribute additional information towards building more precise paleoclimate models.

Abstract Digital leaf physiognomy (DLP) is considered as one of the most promising methods for estimating past climate. However, current models built using the DLP data set still lack precision, especially for mean annual precipitation (MAP). To improve predictive power, we developed five machine learning (ML) models for mean annual temperature (MAT) and MAP respectively, and then tested the precision of these models and some of their averaging compared with that obtained from other models. The precision of all models was assessed using a repeated stratified 10‐fold cross‐validation. For MAT, three combinations of models ( R 2 = .77) presented moderate improvements in precision over the multiple linear regression (MLR) model ( R 2 = .68). For log e (MAP), the averaging of the support vector machine (SVM) and boosting models improved the R 2 from .19 to .63 compared with that of the MLR model. For MAP, the R 2 of this model combination was 0.49, which was much better than that of the artificial neural network (ANN) model ( R 2 = .21). Even the bagging model, which had the lowest R 2 (.37) for log e (MAP), demonstrated better precision ( R 2 = .27) for MAP. Our palaeoclimate estimates for nine fossil floras were also more accurate, because they were in better agreement with independent paleoclimate evidence. Our study confirms that our ML models and their averaging can improve paleoclimatic reconstructions, providing a better understanding of the relationship between climate and leaf physiognomy.

Abstract Vegetation restoration has been proposed as an effective measure for rehabilitating degraded land and slowing desertification in arid regions. However, the spatial variation in soil quality and plant diversity following vegetation restoration remains unclear. This study was designed to explore soil nutrient dynamics and how soil nutrients affect plant diversity and spatial heterogeneity after shrub restoration. We assessed the effect of Haloxylon ammodendron (C.A.Mey.) Bunge (which has been planted over 30 years) on the soil nutrients and plant diversity in a desert–oasis ecotone in Minqin County, Gansu, China, using geostatistics, beta diversity and rarefaction analyses, and Hill number extrapolation. Soil nutrients, including soil organic matter, total nitrogen, and alkali nitrogen, increased significantly after H. ammodendron planting. Species richness gradually increased from 1–5 years to 10–20 years after H. ammodendron was planted but then decreased at 20–30 years. The largest differences in plant composition were observed at 15 and 20 years. Plant diversity increased in the whole 30 years after shrub planting, increasing in the first 25 years and then decreasing at 26–30 year stage. The maximum coefficient of determination for the spatial heterogeneity model fit was 0.84 (25 years). The spatial heterogeneity in vegetation decreased with increasing soil available K content at 1–10 years. Our results suggest that planting shrubs can improve soil conditions and plant species diversity in desert–oasis ecotones and soil nutrients have a strong influence on plant diversity patterns and spatial heterogeneity following vegetation restoration.