Responses of boreal conifers to climate fluctuations: indications from tree-ring widths and carbon isotope analyses

1998 ◽  
Vol 28 (4) ◽  
pp. 524-533 ◽  
Author(s):  
J Renée Brooks ◽  
Lawrence B Flanagan ◽  
James R Ehleringer

Spatial distribution and species composition of the boreal forest are expected to change under predicted climate change scenarios. Current research indicates that water limitations control the southern boundary of the central Canadian boreal forest and temperature limitations control the northern boundary. As part of Boreal Ecosystem - Atmosphere Study (BOREAS), we examined this idea by comparing annual variation in tree-ring widths and carbon isotope ratios ( delta 13C) of tree-ring cellulose with annual climatic parameters in the northern and southern boreal forest. Contrary to expectations, climate correlations with ring widths at the northern and southern sites were similar in black spruce (Picea mariana (Mill.) BSP). Annual growth was favored by cooler and wetter conditions. For jack pine (Pinus banksiana Lamb.), increased temperature and spring precipitation favored annual growth at both sites. In the north, annual growth was negatively correlated with winter precipitation. The delta 13C - climate correlations in Pinus banksiana followed current distribution theories. In the south, potential evapotranspiration explained significant annual delta 13C variation, whereas in the north, winter and growing season precipitation influenced annual delta 13C variations. Our data support the concept that moisture limits the southern range of Pinus banksiana and cold soil temperatures limit the northern extent. However, colder, wetter conditions favored growth of Picea mariana throughout its range. These observations strengthen the concept that species respond individually to climate change, not as a cohesive biome.

Forests ◽  
2020 ◽  
Vol 11 (5) ◽  
pp. 525
Author(s):  
Keliang Zhang ◽  
Lanping Sun ◽  
Jun Tao

Analyzing the effects of climate change on forest ecosystems and individual species is of great significance for incorporating management responses to conservation policy development. Euscaphis japonica (Staphyleaceae), a small tree or deciduous shrub, is distributed among the open forests or mountainous valleys of Vietnam, Korea, Japan, and southern China. Meanwhile, it is also used as a medicinal and ornamental plant. Nonetheless, the extents of E. japonica forest have gradually shrunk as a result of deforestation, together with the regional influence of climate change. The present study employed two methods for modeling species distribution, Maxent and Genetic Algorithm for Rule-set Prediction (GARP), to model the potential distribution of this species and the effects of climate change on it. Our results suggest that both models performed favorably, but GARP outperformed Maxent for all performance metrics. The temperate and subtropical regions of eastern China where the species had been recorded was very suitable for E. japonica growth. Temperature and precipitation were two primary environmental factors affecting the distribution of E. japonica. Under climate change scenarios, the range of suitable habitats for E. japonica will expand geographically toward the north. Our findings may be used in several ways such as identifying currently undocumented locations of E. japonica, sites where it may occur in the future, or potential locations where the species could be introduced and so contribute to the conservation and management of this species.


2014 ◽  
Vol 955-959 ◽  
pp. 3777-3782 ◽  
Author(s):  
Xiao Feng Zhao ◽  
Bin Le Lin

We evaluated land suitability for Jatropha cultivation at a global scale under current and future climate scenarios. Areas that are suitable for Jatropha cultivation include southern South America, the west and southeast coasts of Africa, the north of South Asia, and the north and south coasts of Australia. In the predicted climate change scenarios, areas near the equator become less suitable for Jatropha cultivation, and areas further from the equator become more suitable. Our analyses suggest that the rank order of the six climate change scenarios, from the smallest to the largest effects on Jatropha cultivation, was as follows: B1, A1T/B2, A1B, A2, and A1FI.


2008 ◽  
Vol 15 ◽  
pp. 57-60 ◽  
Author(s):  
Peter Rasmussen ◽  
Mikkel Ulfeldt Hede ◽  
Nanna Noe-Nygaard ◽  
Annemarie L. Clarke ◽  
Rolf D. Vinebrooke

The need for accurate predictions of future environmental change under conditions of global warming has led to a great interest in the most pronounced climate change known from the Holocene: an abrupt cooling event around 8200 years before present (present = A.D. 1950), also known as the ‘8.2 ka cooling event’ (ka = kilo-annum = 1000 years). This event has been recorded as a negative δ18O excursion in the central Greenland ice cores (lasting 160 years with the lowest temperature at 8150 B.P.; Johnsen et al. 1992; Dansgaard 1993; Alley et al. 1997; Thomas et al. 2007) and in a variety of other palaeoclimatic archives including lake sediments, ocean cores, speleothems, tree rings, and glacier oscillations from most of the Northern Hemisphere (e.g. Alley & Ágústsdóttir 2005; Rohling & Pälike 2005). In Greenland the maximum cooling was estimated to be 6 ± 2°C (Alley et al. 1997) while in southern Fennoscandia and the Baltic countries pollenbased quantitative temperature reconstructions indicate a maximum annual mean temperature decrease of around 1.5°C (e.g. Seppä et al. 2007). Today there is a general consensus that the primary cause of the cooling event was the final collapse of the Laurentide ice sheet near Hudson Bay and the associated sudden drainage of the proglacial Lake Agassiz into the North Atlantic Ocean around 8400 B.P. (Fig. 1; Barber et al. 1999; Kleiven et al. 2008). This freshwater outflow, estimated to amount to c. 164,000 km3 of water, reduced the strength of the North Atlantic thermohaline circulation and thereby the heat transported to the North Atlantic region, resulting in an atmospheric cooling (Barber et al. 1999; Clark et al. 2001; Teller et al. 2002). The climatic consequences of this meltwater flood are assumed to be a good geological analogue for future climate-change scenarios, as a freshening of the North Atlantic is projected by almost all global-warming models (e.g. Wood et al. 2003; IPCC 2007) and is also currently being registered in the region (Curry et al. 2003). In an ongoing project, the influence of the 8.2 ka cooling event on a Danish terrestrial and lake ecosystem is being investigated using a variety of biological and geochemical proxy data from a sediment core extracted from Højby Sø, north-west Sjælland (Fig. 2). Here we present data on changes in lake hydrology and terrestrial vegetation in response to climate change, inferred from macrofossil data and pollen analysis, respectively.


IAWA Journal ◽  
2020 ◽  
Vol 41 (2) ◽  
pp. 202-218
Author(s):  
Jeong-Wook Seo ◽  
Dieter Eckstein ◽  
Allan Buras ◽  
Jörg Fromm ◽  
Martin Wilmking ◽  
...  

Abstract Although cell-anatomical variables are promising proxies reflecting seasonal as well as annual climate changes, their interdependencies are not yet fully understood. In the present study we assessed the changes in tree-ring width and various wood anatomical traits, including wall thickness, lumen diameter and tracheid diameter in the radial direction in saplings of Pinus sylvestris under six climatic conditions: 5°C warmer alone (ET) or combined with drought in June (ETJ) and in August (ETA) and CO2 enrichment alone (EC, 770 ppm) or combined with drought in June (ECJ) and in August (ECA). The experiments related to temperature conditions using 2-year saplings and CO2 conditions using 3-year saplings were completed in 2009 and 2010 in a greenhouse, respectively. Results showed that tree-ring width and tracheid diameter were not affected by any of the conditions applied, but the lumen diameter was larger and the wall thickness was thinner than those under control conditions. These reactions were verified under ETJ in the warming treatment and under all conditions under CO2 enrichment conditions. Our results indicated that drought counteracted the effects of elevated CO2 concentrations on wood anatomical properties, signifying complex interactions between the two major effects of climate change. Our comparison of wood parameters through experiments highlight the potential effect of climate change — increased drought stress due to higher temperatures and water shortage as well as elevated ambient CO2, on tracheid lumen diameter and wall thickness. Whereas the ring-width and tracheid diameter practically remained unaffected under the above-mentioned conditions.


2018 ◽  
Vol 15 (5) ◽  
pp. 1319-1333 ◽  
Author(s):  
Michael Klinge ◽  
Choimaa Dulamsuren ◽  
Stefan Erasmi ◽  
Dirk Nikolaus Karger ◽  
Markus Hauck

Abstract. In northern Mongolia, at the southern boundary of the Siberian boreal forest belt, the distribution of steppe and forest is generally linked to climate and topography, making this region highly sensitive to climate change and human impact. Detailed investigations on the limiting parameters of forest and steppe in different biomes provide necessary information for paleoenvironmental reconstruction and prognosis of potential landscape change. In this study, remote sensing data and gridded climate data were analyzed in order to identify main distribution patterns of forest and steppe in Mongolia and to detect environmental factors driving forest development. Forest distribution and vegetation vitality derived from the normalized differentiated vegetation index (NDVI) were investigated for the three types of boreal forest present in Mongolia (taiga, subtaiga and forest–steppe), which cover a total area of 73 818 km2. In addition to the forest type areas, the analysis focused on subunits of forest and nonforested areas at the upper and lower treeline, which represent ecological borders between vegetation types. Climate and NDVI data were analyzed for a reference period of 15 years from 1999 to 2013. The presented approach for treeline delineation by identifying representative sites mostly bridges local forest disturbances like fire or tree cutting. Moreover, this procedure provides a valuable tool to distinguish the potential forested area. The upper treeline generally rises from 1800 m above sea level (a.s.l.) in the northeast to 2700 m a.s.l. in the south. The lower treeline locally emerges at 1000 m a.s.l. in the northern taiga and rises southward to 2500 m a.s.l. The latitudinal gradient of both treelines turns into a longitudinal one on the eastern flank of mountain ranges due to higher aridity caused by rain-shadow effects. Less productive trees in terms of NDVI were identified at both the upper and lower treeline in relation to the respective total boreal forest type area. The mean growing season temperature (MGST) of 7.9–8.9 ∘C and a minimum MGST of 6 ∘C are limiting parameters at the upper treeline but are negligible for the lower treeline. The minimum of the mean annual precipitation (MAP) of 230–290 mm yr−1 is a limiting parameter at the lower treeline but also at the upper treeline in the forest–steppe ecotone. In general, NDVI and MAP are lower in grassland, and MGST is higher compared to the corresponding boreal forest. One exception occurs at the upper treeline of the subtaiga and taiga, where the alpine vegetation consists of mountain meadow mixed with shrubs. The relation between NDVI and climate data corroborates that more precipitation and higher temperatures generally lead to higher greenness in all ecological subunits. MGST is positively correlated with MAP of the total area of forest–steppe, but this correlation turns negative in the taiga. The limiting factor in the forest–steppe is the relative humidity and in the taiga it is the snow cover distribution. The subtaiga represents an ecological transition zone of approximately 300 mm yr−1 precipitation, which occurs independently from the MGST. Since the treelines are mainly determined by climatic parameters, the rapid climate change in inner Asia will lead to a spatial relocation of tree communities, treelines and boreal forest types. However, a direct deduction of future tree vitality, forest composition and biomass trends from the recent relationships between NDVI and climate parameters is challenging. Besides human impact, it must consider bio- and geoecological issues like, for example, tree rejuvenation, temporal lag of climate adaptation and disappearing permafrost.


1999 ◽  
Vol 29 (9) ◽  
pp. 1333-1346 ◽  
Author(s):  
Annika Hofgaard ◽  
Jacques Tardif ◽  
Yves Bergeron

To decipher spatial and temporal tree-growth responses to climate change we used tree-ring data from Picea mariana (Mill.) BSP and Pinus banksiana Lamb. along a latitudinal transect in western Quebec. The transect encompassed the distinct transition between mixed and coniferous forests at approximately 49°N. Correlation analyses and principal component analyses were used to identify common spatiotemporal growth patterns, and site- and species-specific patterns since 1825. A moist summer in the year t - 1 and an early start of the current growing season favored growth of both species. A prolongation of the growing season into fall was the most distinguishing factor between the species. A long and gradual climatic gradient shifted to a short gradient with a clear segregation between the southern and northern parts of the transect. This shift, around 1875, was abrupt and characterized by a turbulent climatic period. The observed pattern was likely related to a large-scale shift in the mean position of the Arctic Front that occurred at the end of the 1800s. No discrete climatic setting explained the present switch from mixedwoods to conifers at 49°N. Awareness of such nonequilibrial relations between climate and species distribution is essential when assessing vegetation responses to future climate change.


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