Warming induced tree-growth decline of Toona ciliata in (sub-) tropical southwestern China

Tropical forests play an important role in the global carbon cycle and climate regulation. However, our understanding of how Asian tropical forest growth responds to climatic variations is still limited. We developed tree ring-width chronologies of Toona ciliata from 90 trees (139 cores) from two study regions in the tropical/subtropical forests in Yunnan, southwestern China. Bootstrapped correlation analysis revealed positive moisture sensitivity (precipitation, self-calibrated Palmer drought severity index, relative humidity, and soil moisture) and negative temperature sensitivity of T. ciliata, and the relationship was strongest during dry and/or dry-to-wet transition months, indicating that radial growth of T. ciliata is primarily limited by moisture availability during early growing season. Furthermore, radial growth of T. ciliata was significantly and negatively correlated with the vapor pressure deficit and potential evapotranspiration during dry and/or dry-to-wet transition months. We analyzed long-term growth trends of T. ciliata using ‘size class isolation' (SCI) and ‘generalized additive mixed models' (GAMM) approaches which remove the effects of tree size on tree growth. We detected decreasing growth trend for both approaches at both study regions, indicating that the growth decline of T. ciliata stands in southwestern China is likely due to global warming-induced moisture deficit. The growth of T. ciliata trees is likely to continually decline under projected warming and drying conditions. The observed growth declines of T. ciliata raised concerns about developing sustainable management and conservation programs for tropical/subtropical forests in China.     

Long Tree-Ring Chronologies Provide Evidence of Recent Tree Growth Decrease in a Central African Tropical Forest

It is still unclear whether the exponential rise of atmospheric CO₂ concentration has produced a fertilization effect on tropical forests, thus incrementing their growth rate, in the last two centuries. As many factors affect tree growth patterns, short -term studies might be influenced by the confounding effect of several interacting environmental variables on plant growth. Long-term analyses of tree growth can elucidate long-term trends of plant growth response to dominant drivers. The study of annual rings, applied to long tree-ring chronologies in tropical forest trees enables such analysis. Long-term tree-ring chronologies of three widespread African species were measured in Central Africa to analyze the growth of trees over the last two centuries. Growth trends were correlated to changes in global atmospheric CO₂ concentration and local variations in the main climatic drivers, temperature and rainfall. Our results provided no evidence for a fertilization effect of CO₂ on tree growth. On the contrary, an overall growth decline was observed for all three species in the last century, which appears to be significantly correlated to the increase in local temperature. These findings provide additional support to the global observations of a slowing down of C sequestration in the trunks of forest trees in recent decades. Data indicate that the CO₂ increase alone has not been sufficient to obtain a tree growth increase in tropical trees. The effect of other changing environmental factors, like temperature, may have overridden the fertilization effect of CO₂.     

Recent growth increase in endemic Juglans boliviana from the tropical Andes

The spatial coverage of tree-ring chronologies in tropical South America is low compared to the extratropics, particularly in remote regions. Tree-ring dating from such tropical sites is limited by the generally weak temperature seasonality, complex coloration, and indistinct anatomical morphology in some tree species. As a result, there is a need to complement traditional methods of dendrochronology with innovative and independent approaches. Here, we supplement traditional tree-ring methods via the use of radiocarbon analyses to detect partial missing rings and/or false rings, and wood anatomical techniques to precisely delineate tree-ring boundaries. In so doing we present and confirm the annual periodicity of the first tree-ring width (TRW) chronology spanning from 1814 to 2017 for Juglans boliviana (‘nogal’), a tree species growing in a mid-elevation tropical moist forest in northern Bolivia. We collected 25 core samples and 4 cross-sections from living and recently harvested canopy-dominant trees, respectively. The sampled trees were growing in the Madidi National Park and had a mean age of 115 years old, with certain trees growing for over 200 years. Comparison of (residual and standard) TRW chronologies to monthly climate variables shows significant negative relationships to prior year May-August maximum temperatures (r = −0.54, p < 0.05) and positive relationships to dry season May-October precipitation (r = 0.60, p < 0.05) before the current year growing season. Additionally, the radial growth of Juglans boliviana shows a significant positive trend since 1979. Our findings describe a new and promising tree species for dendrochronology due to its longevity and highlight interdisciplinary techniques that can be used to expand the current tree-ring network in Bolivia and the greater South American tropics.     

Age structure and climate sensitivity of a high Andean relict forest of Polylepis rodolfo-vasquezii in central Peru

For a better understanding of forest ecology, tree-ring studies can provide information on climate sensitivity, tree growth patterns and population age structure that can inform about stand dynamics such as recruitment of new individuals, and other interspecific interactions related to competition and facilitation. Little is known about the ecology of the recently identified high Andean tree species Polylepis rodolfo-vasquezii. Here, we analyzed the relationship between tree size and age of two P. rodolfo-vasquezii forest stands located in the central Peruvian Andes at 11°S in latitude, and compared their growth patterns and climate sensitivity. We measured the height and diameter of each individual tree and collected tree core samples of living trees and cross sections of dead standing trees to generate two centennial tree-ring chronology at Toldopampa (1825–2015 CE) and at Pomamanta (1824–2014 CE) sites. The dendrochronological dates were evaluated by ¹⁴C analysis using the bomb-pulse methods analyzing a total of 9 calendar years that confirm the annual periodicity of this tree species. At the Toldopampa stand most trees ranged from 70 to 80 years old, with a 190-year old individual, being an older and better preserve forest than Pomamanta, with younger trees, probably because more human disturbances due to closer village proximity. No significant relationships were found between tree age and size in the oldest stand alerting that tree diameter should not be used as a metric for estimating tree ages as a general rule. The distinct growth patterns and the size-age relationship observed at the two forests may reflect distinct histories regarding human activities such as fire and logging. Nevertheless, both the Toldopampa and the Pomamanta tree-ring width chronologies exhibited common growth patterns and shared a similar positive response to temperature of the current growing season. Overall, our study confirmed the annual radial growth periodicity in P. rodofolfo-vasquezii trees using an independent method such as ¹⁴C analyses and a strong climate sensitivity of this tree species. These findings encourage the development of an extensive P. rodolfo-vasquezii tree-ring network for ecological and paleoclimate studies in the tropical Andes in South America.     

Significant Mean and Extreme Climate Sensitivity of Norway Spruce and Silver Fir at Mid-Elevation Mesic Sites in the Alps

Climate forcing is the major abiotic driver for forest ecosystem functioning and thus significantly affects the role of forests within the global carbon cycle and related ecosystem services. Annual radial increments of trees are probably the most valuable source of information to link tree growth and climate at long-term time scales, and have been used in a wide variety of investigations worldwide. However, especially in mountainous areas, tree-ring studies have focused on extreme environments where the climate sensitivity is perhaps greatest but are necessarily a biased representation of the forests within a region. We used tree-ring analyses to study two of the most important tree species growing in the Alps: Norway spruce (Picea abies) and silver fir (Abies alba). We developed tree-ring chronologies from 13 mesic mid-elevation sites (203 trees) and then compared them to monthly temperature and precipitation data for the period 1846–1995. Correlation functions, principal component analysis and fuzzy C-means clustering were applied to 1) assess the climate/growth relationships and their stationarity and consistency over time, and 2) extract common modes of variability in the species responses to mean and extreme climate variability. Our results highlight a clear, time-stable, and species-specific response to mean climate conditions. However, during the previous-year''s growing season, which shows the strongest correlations, the primary difference between species is in their response to extreme events, not mean conditions. Mesic sites at mid-altitude are commonly underrepresented in tree-ring research; we showed that strong climatic controls of growth may exist even in those areas. Extreme climatic events may play a key role in defining the species-specific responses on climatic sensitivity and, with a global change perspective, specific divergent responses are likely to occur even where current conditions are less limited.     

Dendroecology in the tropics: a review

Over the last decade the field of tropical dendroecology has developed rapidly and major achievements have been made. We reviewed the advances in three main themes within the field. First, long chronologies for tropical tree species were constructed which allowed climate reconstructions, revealed sources of climatic variation and clarified climate–growth relations. Other studies combined tree-ring data and stable isotope (¹³C and ¹⁸O) measurements to evaluate the response of tropical trees to climatic variation and changes. A second set of studies assessed long-term growth patterns of individual trees throughout their life. These studies enhanced the understanding of growth trajectories to the canopy, quantified autocorrelated tree growth and yielded new estimates of tree ages. Such studies were also used to reconstruct the disturbance history of tropical forests. The last set of studies applied tree-ring data to growth models. Tree-ring data can replace diameter measurements from research plots, provide additional information to construct population models, improve timber yield models and validate model output. Based on our review, we propose two main directions for future research. (1) An evaluation of the causes and consequences of growth variation within and among trees and their relation to environmental variation. Studies evaluating this directly contribute to improved understanding of tropical tree ecology. (2) The simultaneous measurement of widths and stable isotope fractions in tree rings offers the potential to study responses of trees to climatic change. Given the major role of tropical forests in the global carbon cycle, knowing these responses is of high priority.     

Climate-growth relations of congeneric tree species vary across a tropical vegetation gradient in Brazil

Seasonally dry tropical forests are an important global climatic regulator, a main driver of the global carbon sink dynamics and are predicted to suffer future reductions in their productivity due to climate change. Yet, little is known about how interannual climate variability affects tree growth and how climate-growth responses vary across rainfall gradients in these forests. Here we evaluate changes in climate sensitivity of tree growth along an environmental gradient of seasonally dry tropical vegetation types (evergreen forest – savannah – dry forest) in Northeastern Brazil, using congeneric species of two common neotropical genera: Aspidosperma and Handroanthus. We built tree-ring width chronologies for each species × forest type combinations and explored how growth variability correlated with local (precipitation, temperature) and global (the El Niño Southern Oscillation - ENSO) climatic factors. We also assessed how growth sensitivity to climate and the presence of growth deviations varied along the gradient. Precipitation stimulates tree growth and was the main growth-influencing factor across vegetation types. Trees in the dry forest site showed highest growth sensitivity to interannual variation in precipitation. Temperature and ENSO phenomena correlated negatively with growth and sensitivity to both climatic factors were similar across sites. Negative growth deviations were present and found mostly in the dry-forest species. Our results reveal a dominant effect of precipitation on tree growth in seasonally dry tropical forests and suggest that along the gradient, dry forests are the most sensitivity to drought. These forests may therefore be the most vulnerable to the deleterious effects of future climatic changes. These results highlight the importance of understanding the climatic sensitivity of different tropical forests. This understanding is key to predict the carbon dynamics in tropical regions, and sensitivity differences should be considered when prioritizing conservation measures of seasonally dry topical forests.     

What tree rings can tell us about the competition between trees and lianas? A case study based on growth,anatomy, density,and carbon accumulation

In tropical forest, landscape fragmentation and the consequent degradation of disturbed forests increase the incidence of light and dry hot winds, causing a disturbance on natural regeneration. Under these conditions, lianas (woody vines) development is stimulated instead of other species, which are more suited to mature forest and under less influence of the edge effect. For this, lianas colonization is an important variable for assessing the disturbance level of a forest. In this context, it becomes important to understand the nature of the competitive relationships between hyper-abundant lianas and ring growth of the host trees. Here, we selected trees with occupation or absence of lianas from two tropical species – Pinus caribaea var. hondurensis (Caribbean pine) and Tectona grandis (teak) – localized in a semideciduous forest fragment in southeastern Brazil, aiming to compare growth, climatic response, anatomy (vessels and intra-annual density fluctuations), wood density and carbon, by tree-ring analysis. The results showed that the lianas caused a change in tree-ring anatomy of host trees in last 10 years, mainly. We observed that trees occupied by lianas had a decrease the radial growth and carbon in the two species, an increase of the vessels size in teak and a decrease of the IADF frequency in Caribbean pine. In teak, the climate-tree relationship indicated that trees with lianas had lower response to rainfall and higher response to temperature in the summer (rainy and hottest period); in Caribbean pine, we observed that trees with lianas had a 2-month delay in the radial growth response to rainfall in the dry season. In the teak group, we observed that host trees had higher wood density values than liana-free tree in the outer rings, and the opposite was showed for pine. These findings show that tree-ring growth of host trees are a strong bioindicator of forest disturbance caused by aggressive colonization of lianas. We believe that these methods are applicable to future studies relating to the effects of habitat fragmentation and forest degradation on biodiversity and ecosystem services, particularly in the context of global climate change.     

Recent decline of high altitude coniferous growth due to thermo-hydraulic constrains: evidence from the Miyaluo Forest Reserve,Western Sichuan Plateau of China

Tree growth decline has been reported in many places around the globe under the context of increasingly warming climate, and strengthening drought intensity is detected to be the primary factor for such decline, particularly in northern forest sites, as well as arid and semi-arid areas. Yet, the forest growth decline in high altitude, high mountain sites certainly merits investigation. Here, we reported faxon fir (Abies fargesii var. faxoniana) forest growth decline (slope = -0.64) at the tree line (4150 m above sea level) in Miyaluo Forest Reserve (MFR) at the Western Sichuan Plateau, southwestern China since 2000. We investigated the cause of tree growth decline by applying dendrochronological approaches. We took tree-ring samples from fir trees at the tree line and developed tree-ring width (TRW) chronology. The tree growth – climate relationship analysis showed that maximum temperature (Tmax) was the primary factor limiting the radial growth of fir trees in the investigated area. The moving correlation analysis indicated the strengthening positive influence of Tmax, spring precipitation, and cloud cover during winter and monsoon period on radial growth since 2000s. Our results have shown that both thermal and hydraulic constrains accounted for the radial growth decline of fir trees at the tree line of MFR in the western Sichuan Plateau.     

Long‐term increases in intrinsic water‐use efficiency do not lead to increased stem growth in a tropical monsoon forest in western Thailand

Rising atmospheric carbon dioxide [CO₂] can accelerate tree growth by stimulating photosynthesis and increasing intrinsic water‐use efficiency (iWUE). Little evidence exists, however, for the long‐term growth and gas‐exchange responses of mature trees in tropical forests to the combined effects of rising [CO₂] and other global changes such as warming. Using tree rings and stable isotopes of carbon and oxygen, we investigated long‐term trends in the iWUE and stem growth (basal area increment, BAI) of three canopy tree species in a tropical monsoon forest in western Thailand (Chukrasia tabularis, Melia azedarach, and Toona ciliata). To do this, we modelled the contribution of ontogenetic effects (tree diameter or age) and calendar year to variation in iWUE, oxygen isotopes, and BAI using mixed‐effects models. Although iWUE increased significantly with both tree diameter and calendar year in all species, BAI at a given tree diameter was lower in more recent years. For one species, C. tabularis, differences in crown dominance significantly influence stable isotopes and growth. Tree ring Δ¹⁸O increased with calendar year in all species, suggesting that increasing iWUE may have been driven by relatively greater reductions in stomatal conductance – leading to enrichment in Δ¹⁸O – than increases in photosynthetic capacity. Plausible explanations for the observed declines in growth include water stress resulting from rising temperatures and El Niño events, increased respiration, changes in allocation, or more likely, a combination of these factors.     

Assessing cross-datable distinct annual growth rings in non-native Pinus kesiya Royle ex Gordon in Zambia

The response of non-native forest plantation trees to climate change remains poorly understood.We hypothesized that precipitation and temperature modulate tree-ring width chronology at each site and that higher tree growth is exhibited at remote sites than sites near copper mines. This study investigates if the annual tree-ring boundaries in non-native Pinus kesiya Royle ex Gordon in Zambia are distinct, cross-datable, and coherent with climate signal. We collected increment cores from live trees and climate data near and further away from emission sources and developed site tree-ring width chronologies. Based on cross-dating and chronology building statistics (i.e., ESP > 0.85; Glk > 0.6 and series inter-correlation > 0.4), P. kesiya posses cross-datable distinct annual growth ring boundaries that exhibited a high climate signal at both sites. The tree-ring width chronology was positively modulated by precipitation and negatively by solar radiation and temperature. The dry season precipitation was the limiting factor for the growth of P. kesiya. The predicted decrease in dry season precipitation and increase in temperature and solar radiation may reduce tree growth of P. kesiya, reduce productivity, and extend the rotation age. The mean ring width in P. kesiya was not significantly (p = 0.296) different between sites. However, the mean basal area increment at the site near the emission source (Ichimpe) was significantly (p < 0.001) higher than at the remote site (Chati), suggesting site-specific influences that require investigation. We recommend evaluating the causes and consequences of tree growth variation between sites and their relation to environmental variation, including microclimate, soils, and pollution. In this regard, an assessment of site-specific ring-width chronology and tree growth variation in this study directly contributes to an improved understanding of non-native P. kesiya ecology, and it offers the potential to study trees' responses to edaphic and climatic factors. Knowing these responses deepens our understanding of non-native pine tree growth in the face of climate change, given the significant role of tropical forests in the global carbon cycle.     

Community and ecosystem ramifications of increasing lianas in neotropical forests

Lianas (woody vines) are increasing in neotropical forests, representing one of the first large-scale structural changes documented for these important ecosystems. The potential ramifications of increasing lianas are huge, as lianas alter both tropical forest diversity and ecosystem functioning. At the community level, lianas affect tree species co-existence and diversity by competing more intensely with some tree species than others, and thus will likely alter tree species composition. At the ecosystem level, lianas affect forest carbon and nutrient storage and fluxes. A decrease in forest carbon storage and sequestration may be the most important ramification of liana increases. Lianas reduce tree growth and increase tree mortality—thus reducing forest-level carbon storage. The increase in lianas, which have much less wood than trees, compensates only partially for the amount of carbon lost in the displaced trees. Because tropical forests contribute approximately one-third of global terrestrial carbon stocks and net primary productivity, the effect of increasing lianas for tropical forest carbon cycles may have serious repercussions at the global scale.Key words: carbon cycle, CO₂, disturbance, global change, land use change, liana increases, structural changes, tropical forestsTropical forests contain most of the earth''s plant species and contribute more to carbon storage in the form of above ground biomass than any other terrestrial ecosystem. Temperate and boreal forests are changing rapidly in response to global anthropogenic drivers. Similar large-scale changes are now being detected in tropical forests. One of the largest contemporary changes in tropical forests is an increase in lianas (woody vines),¹ which could have serious consequences for tree species diversity and composition, as well as the reducing capacity of tropical forests to store carbon.^1–3     

No evidence for consistent long‐term growth stimulation of 13 tropical tree species: results from tree‐ring analysis

The important role of tropical forests in the global carbon cycle makes it imperative to assess changes in their carbon dynamics for accurate projections of future climate–vegetation feedbacks. Forest monitoring studies conducted over the past decades have found evidence for both increasing and decreasing growth rates of tropical forest trees. The limited duration of these studies restrained analyses to decadal scales, and it is still unclear whether growth changes occurred over longer time scales, as would be expected if CO₂‐fertilization stimulated tree growth. Furthermore, studies have so far dealt with changes in biomass gain at forest‐stand level, but insights into species‐specific growth changes – that ultimately determine community‐level responses – are lacking. Here, we analyse species‐specific growth changes on a centennial scale, using growth data from tree‐ring analysis for 13 tree species (~1300 trees), from three sites distributed across the tropics. We used an established (regional curve standardization) and a new (size‐class isolation) growth‐trend detection method and explicitly assessed the influence of biases on the trend detection. In addition, we assessed whether aggregated trends were present within and across study sites. We found evidence for decreasing growth rates over time for 8–10 species, whereas increases were noted for two species and one showed no trend. Additionally, we found evidence for weak aggregated growth decreases at the site in Thailand and when analysing all sites simultaneously. The observed growth reductions suggest deteriorating growth conditions, perhaps due to warming. However, other causes cannot be excluded, such as recovery from large‐scale disturbances or changing forest dynamics. Our findings contrast growth patterns that would be expected if elevated CO₂ would stimulate tree growth. These results suggest that commonly assumed growth increases of tropical forests may not occur, which could lead to erroneous predictions of carbon dynamics of tropical forest under climate change.     

Size-dependent responses to summer drought in Scots pine, Norway spruce and common oak

In this study, we provide a detailed analysis of tree growth and water status in relation to climate of three major species of forest trees in lower regions of Bavaria, Southern Germany: Scots pine (Pinus sylvestris), Norway spruce (Picea abies) and common oak (Quercus robur). Tree-ring chronologies and latewood δ¹³C were used to derive measures for drought reaction across trees of different dimensions: growth reduction associated with drought years, long-term growth/climate relations and stomatal control on photosynthesis. For Scots pine, growth/climate relations indicated a stronger limitation of radial growth by high summer temperatures and low summer precipitation in smaller trees in contrast to larger trees. This is corroborated by a stronger stomatal control on photosynthesis for smaller pine trees under average conditions. In dry years, however, larger pine trees exhibited stronger growth reductions. For Norway spruce, a significantly stronger correlation of tree-ring width with summer temperatures and summer precipitation was found for larger trees. Additionally, for Norway spruce there is evidence for a change in competition mode from size-asymmetric competition under conditions with sufficient soil water supply to a more size-symmetric competition under dry conditions. Smaller oak trees showed a weaker stomatal control on photosynthesis under both dry and average conditions, which is also reflected by a significantly faster recovery of tree-ring growth after extreme drought events in smaller oak trees. The observed patterns are discussed in the context of the limitation-caused matter partitioning hypothesis and possible species-specific ontogenetic modifications.     

Variability in solar radiation and temperature explains observed patterns and trends in tree growth rates across four tropical forests

The response of tropical forests to global climate variability and change remains poorly understood. Results from long-term studies of permanent forest plots have reported different, and in some cases opposing trends in tropical forest dynamics. In this study, we examined changes in tree growth rates at four long-term permanent tropical forest research plots in relation to variation in solar radiation, temperature and precipitation. Temporal variation in the stand-level growth rates measured at five-year intervals was found to be positively correlated with variation in incoming solar radiation and negatively related to temporal variation in night-time temperatures. Taken alone, neither solar radiation variability nor the effects of night-time temperatures can account for the observed temporal variation in tree growth rates across sites, but when considered together, these two climate variables account for most of the observed temporal variability in tree growth rates. Further analysis indicates that the stand-level response is primarily driven by the responses of smaller-sized trees (less than 20 cm in diameter). The combined temperature and radiation responses identified in this study provide a potential explanation for the conflicting patterns in tree growth rates found in previous studies.     

Slow lifelong growth predisposes Populus tremuloides trees to mortality

Widespread dieback of aspen forests, sometimes called sudden aspen decline, has been observed throughout much of western North America, with the highest mortality rates in the southwestern United States. Recent aspen mortality has been linked to drought stress and elevated temperatures characteristic of conditions expected under climate change, but the role of individual aspen tree growth patterns in contributing to recent tree mortality is less well known. We used tree-ring data to investigate the relationship between an individual aspen tree’s lifetime growth patterns and mortality. Surviving aspen trees had consistently higher average growth rates for at least 100 years than dead trees. Contrary to observations from late successional species, slow initial growth rates were not associated with a longer lifespan in aspen. Aspen trees that died had slower lifetime growth and slower growth at various stages of their lives than those that survived. Differences in average diameter growth between live and dead trees were significant (α = 0.05) across all time periods tested. Our best logistical model of aspen mortality indicates that younger aspen trees with lower recent growth rates and higher frequencies of abrupt growth declines had an increased risk of mortality. Our findings highlight the need for species-specific mortality functions in forest succession models. Size-dependent mortality functions suitable for late successional species may not be appropriate for species with different life history strategies. For some early successional species, like aspen, slow growth at various stages of the tree’s life is associated with increased mortality risk.     

Toward consistent measurements of carbon accumulation: A multi-site assessment of biomass and basal area increment across Europe

The use of tree-ring data in carbon cycle research has so far been limited because traditional study designs are not geared toward quantifying forest carbon accumulation. Existing studies that assessed biomass increment from tree rings were often confined to individual sites and used inconsistent sampling schemes. We applied a consistent biomass-oriented sampling design at five managed forest sites located in different climate zones to assess the annual carbon accumulation in above-ground woody tissues (i.e. stems and branches) and its climate response. Radial growth and biometric measurements were combined to reconstruct the annual biomass increment in individual trees and upscaled to the site level. In addition to this, we estimated that 32–60 trees are required at these five sites to robustly quantify carbon accumulation rates. Tree dimensions and growth rates varied considerably among sites as a function of differing stand density, climatic limitations, and management interventions. Accordingly, mean site-level carbon accumulation rates between 65 g C m⁻² y⁻¹ and 225 g C m⁻² y⁻¹ were reconstructed for the 1970–2009 period. A comparison of biomass increment with the widely used basal area increment (BAI) revealed very similar growth trends but emphasized the merits of biomass assessments due to species-specific BAI/biomass relationship. Our study illustrates the benefits and challenges of combining tree-ring data with biometric measurements and promotes the consistent application of a standardized sampling protocol across large spatial scales. It is thus viewed as a conceptual basis for future use of tree-ring data to approach research questions related to forest productivity and the terrestrial carbon balance.     

Gypsy moth-induced growth decline of Larix sibirica in a forest-steppe ecotone

Effects of a gypsy moth attack on the productivity of Larix sibirica on tree-ring width were analyzed in a case study of a mountain site in the western Khentey in the northern Mongolian forest-steppe ecotone. A major aim of the study was to assess whether reduced productivity by gypsy moth herbivory could contribute to fluctuations of the forest edge to the steppe in larch-dominated woodlands. In the year of the infestation, larch trees at the forest edge lost 90% of their needles and latewood formation was strongly reduced. However, earlywood formation was widely completed before the gypsy moth attack and, therefore, total tree-ring width was not below the average of the five years prior to infestation. In the two years following the gypsy moth invasion, annual stem increment was strongly reduced. Trees growing 30–100 m inside the forest showed a much weaker response of tree-ring widths to the gypsy moth infestation consistent with significantly higher defoliation at forest edge than in the forest interior. Old trees exhibited a stronger growth decline than middle-aged trees, indicating higher infestation of dominant, exposed trees, which are thought to be better accessible to the wind-dispersed gypsy moth larvae hatching in the early growing season on the steppe. Under the current climate, occasional growth reductions are thought to be of little effect on the performance of L. sibirica, as fast-growing competitors of other tree species, which are not or hardly affected by gypsy moth, are absent.     

Drivers of growth variability of Hymenaea stigonocarpa,a widely distributed tree species in the Brazilian Cerrado

Dendrochronology is a valuable tool to understanding climate-growth and growth-age relationships of native tree species from tropical forests. The information obtained from growth rings can elucidate climate responses of tree-growth under the ongoing environmental changes and support the development of sustainable forest management strategies based on species and site conditions. The Cerrado, which is a vast tropical savannah ecoregion of Brazil, has precipitation seasonality capable of inducing the formation of annual tree rings in moisture sensitive woody species. Hymenaea stigonocarpa is the typical tree species in the Cerrado with proven annual tree rings. It is an important commercial species that has been massively exploited for timber causing the considerable reduction of its natural populations. This study provides information about tree age and growth trajectories as well as climatic-growth signals of H. stigonocarpa in southeastern Brazil. We sampled 13 trees for tree-ring analysis. Tree-ring measurement and analysis were conducted using standard dendrochronological techniques. Sampled trees revealed the young successional stage of the stand, with ages varying from 20 to 35 years old. Nine out of 13 trees were used to build the standard chronology (1981 to 2013) that was positively correlated with precipitation at the end of the growing season (March-April). The chronology was able to capture SST anomalies patterns related to the South American Monsoon System. Growth modeling indicated that minimum logging diameter of 10.4cm is achieved at 24 years of age. The results reported here add valuable contribution to the discussion of sustainable management strategies for Cerrado ecoregion species.     

Looking for age-related growth decline in natural forests: unexpected biomass patterns from tree rings and simulated mortality

Forest biomass growth is almost universally assumed to peak early in stand development, near canopy closure, after which it will plateau or decline. The chronosequence and plot remeasurement approaches used to establish the decline pattern suffer from limitations and coarse temporal detail. We combined annual tree ring measurements and mortality models to address two questions: first, how do assumptions about tree growth and mortality influence reconstructions of biomass growth? Second, under what circumstances does biomass production follow the model that peaks early, then declines? We integrated three stochastic mortality models with a census tree-ring data set from eight temperate forest types to reconstruct stand-level biomass increments (in Minnesota, USA). We compared growth patterns among mortality models, forest types and stands. Timing of peak biomass growth varied significantly among mortality models, peaking 20–30 years earlier when mortality was random with respect to tree growth and size, than when mortality favored slow-growing individuals. Random or u-shaped mortality (highest in small or large trees) produced peak growth 25–30 % higher than the surviving tree sample alone. Growth trends for even-aged, monospecific Pinus banksiana or Acer saccharum forests were similar to the early peak and decline expectation. However, we observed continually increasing biomass growth in older, low-productivity forests of Quercus rubra, Fraxinus nigra, and Thuja occidentalis. Tree-ring reconstructions estimated annual changes in live biomass growth and identified more diverse development patterns than previous methods. These detailed, long-term patterns of biomass development are crucial for detecting recent growth responses to global change and modeling future forest dynamics.