David Archer & Victor Brovkin, The millennial atmospheric lifetime
of anthropogenic CO2, Climatic Change (2008)
The notion is pervasive in the climate science community and in the public at
large that the climate impacts of fossil fuel CO2 release will only persist for a few centuries.
This conclusion has no basis in theory or models of the atmosphere/ocean carbon cycle,
which we review here. The largest fraction of the CO2 recovery will take place on time
scales of centuries, as CO2 invades the ocean, but a significant fraction of the fossil fuel
CO2, ranging in published models in the literature from 20–60%, remains airborne for a
thousand years or longer. Ultimate recovery takes place on time scales of hundreds of
thousands of years, a geologic longevity typically associated in public perceptions with
nuclear waste. The glacial/interglacial climate cycles demonstrate that ice sheets and sea
level respond dramatically to millennial-timescale changes in climate forcing. There are
also potential positive feedbacks in the carbon cycle, including methane hydrates in the
ocean, and peat frozen in permafrost, that are most sensitive to the long tail of the fossil fuel
CO2 in the atmosphere.
Alvaro Montenegro et.al., Long term fate of anthropogenic carbon, Geophy Res Let 2007
Two earth-system models of intermediate complexity
are used to study the long term response to an input of
5000 Pg of carbon into the atmosphere. About 75% of CO2
emissions have an average perturbation lifetime of
1800 years and 25% have lifetimes much longer than
5000 years. In the simulations, higher levels of atmospheric
CO2 remain in the atmosphere than predicted by previous
experiments and the average perturbation lifetime of
atmospheric CO2 for this level of emissions is much
longer than the 300–400 years proposed by other studies.
At year 6800, CO2 concentrations between about 960 to
1440 ppmv result in global surface temperature increases
between 6C and 8C. There is also significant surface ocean
acidification, with pH decreasing from 8.16 to 7.46 units
between years 2000 and 2300.
Gerard H. Roe and Marcia B. Baker, Why Is Climate Sensitivity
So Unpredictable? Science
2007 [supporting material]
Uncertainties in projections of future climate change have not lessened substantially in past
decades. Both models and observations yield broad probability distributions for long-term
increases in global mean temperature expected from the doubling of atmospheric carbon dioxide,
with small but finite probabilities of very large increases. We show that the shape of these
probability distributions is an inevitable and general consequence of the nature of the climate
system, and we derive a simple analytic form for the shape that fits recent published distributions
very well. We show that the breadth of the distribution and, in particular, the probability of
large temperature increases are relatively insensitive to decreases in uncertainties associated with
the underlying climate processes.
Reto Knutti and Gabriele C. Hegerl, The equilibrium sensitivity of the Earth’s temperature to radiation changes, Nature Geoscience 2008
The Earth’s climate is changing rapidly as a result of anthropogenic carbon emissions, and damaging
impacts are expected to increase with warming. To prevent these and limit long-term global surface
warming to, for example, 2 °C, a level of stabilization or of peak atmospheric CO2 concentrations
needs to be set. Climate sensitivity, the global equilibrium surface warming after a doubling of
atmospheric CO2 concentration, can help with the translation of atmospheric CO2 levels to warming.
Various observations favour a climate sensitivity value of about 3 °C, with a likely range of about
2–4.5 °C. However, the physics of the response and uncertainties in forcing lead to fundamental
difficulties in ruling out higher values. The quest to determine climate sensitivity has now been going
on for decades, with disturbingly little progress in narrowing the large uncertainty range. However,
in the process, fascinating new insights into the climate system and into policy aspects regarding
mitigation have been gained. The well-constrained lower limit of climate sensitivity and the transient
rate of warming already provide useful information for policy makers. But the upper limit of climate
sensitivity will be more difficult to quantify.
Margaret B. Davis and Ruth G. Shaw, Range Shifts and Adaptive Responses to Quaternary Climate Change, Science 2001
Tree taxa shifted latitude or elevation range in response to changes in
Quaternary climate. Because many modern trees display adaptive differentiation
in relation to latitude or elevation, it is likely that ancient trees
were also so differentiated, with environmental sensitivities of populations
throughout the range evolving in conjunction with migrations. Rapid
climate changes challenge this process by imposing stronger selection and
by distancing populations from environments to which they are adapted.
The unprecedented rates of climate changes anticipated to occur in the
future, coupled with land use changes that impede gene ßow, can be
expected to disrupt the interplay of adaptation and migration, likely
affecting productivity and threatening the persistence of many species.
Petit et. al., Glacial Refugia: Hotspots But Not Melting Pots of Genetic Diversity, Science
2003
Glacial refuge areas are expected to harbor a large fraction of the intraspecific
biodiversity of the temperate biota. To test this hypothesis, we studied chloroplast
DNA variation in 22 widespread European trees and shrubs sampled in the same
forests. Most species had genetically divergent populations in Mediterranean regions,
especially those with low seed dispersal abilities. However, the genetically
most diverse populations were not located in the south but at intermediate latitudes,
a likely consequence of the admixture of divergent lineages colonizing the
continent from separate refugia.
Godfrey Hewitt, The genetic legacy of the Quaternary ice ages, Nature 2000
Global climate has fluctuated greatly during the past three million years, leading to the recent major ice ages. An inescapable consequence for most living organisms is great changes in their distribution, which are expressed differently in boreal, temperate and tropical zones. Such range changes can be expected to have genetic consequences, and the advent of DNA technology provides most suitable markers to examine these. Several good data sets are now available, which provide tests of expectations, insights into species colonization and unexpected genetic subdivision and mixture of species. The genetic structure of human populations may be viewed in the same context. The present genetic structure of populations, species and communities has been mainly formed by Quaternary ice ages, and genetic, fossil and physical data combined can greatly help our understanding of how organisms were so affected.
John W Williams and Stephen T Jackson, Novel climates, no-analog communities, and
ecological surprises, Front Ecol Environ 2007;
No-analog communities (communities that are compositionally unlike any found today) occurred frequently in the
past and will develop in the greenhouse world of the future. The well documented no-analog plant communities of
late-glacial North America are closely linked to “novel” climates also lacking modern analogs, characterized by high
seasonality of temperature. In climate simulations for the Intergovernmental Panel on Climate Change A2 and B1
emission scenarios, novel climates arise by 2100 AD, primarily in tropical and subtropical regions. These future
novel climates are warmer than any present climates globally, with spatially variable shifts in precipitation, and
increase the risk of species reshuffling into future no-analog communities and other ecological surprises. Most ecological
models are at least partially parameterized from modern observations and so may fail to accurately predict
ecological responses to these novel climates. There is an urgent need to test the robustness of ecological models to climate
conditions outside modern experience.
Stephen T. Jackson and Chengyu Weng, Late Quaternary extinction of a tree species in eastern North America, PNAS 1999
Widespread species- and genus-level extinctions of mammals in
North America and Europe occurred during the last deglaciation
[16,000–9,000 yr B.P. (by 14C)], a period of rapid and often abrupt
climatic and vegetational change. These extinctions are variously
ascribed to environmental change and overkill by human hunters.
By contrast, plant extinctions since the Middle Pleistocene are
undocumented, suggesting that plant species have been able to
respond to environmental changes of the past several glacialy
interglacial cycles by migration. We provide evidence from morphological
studies of fossil cones and anatomical studies of fossil
needles that a now-extinct species of spruce (Picea critchfieldii sp.
nov.) was widespread in eastern North America during the Last
Glacial Maximum. P. critchfieldii was dominant in vegetation of the
Lower Mississippi Valley, and extended at least as far east as
western Georgia. P. critchfieldii disappeared during the last deglaciation,
and its extinction is not directly attributable to human
activities. Similarly widespread plant species may be at risk of
extinction in the face of future climate change.
C.W. Woodall at. al., An indicator of tree migration in forests of the eastern United States, Forest Ecology and Management 2009
Changes in tree species distributions are a potential impact of climate change on forest ecosystems. The
examination of tree species shifts in forests of the eastern United States largely has been limited to
simulation activities due to a lack of consistent, long-term forest inventory datasets. The goal of this
study was to compare current geographic distributions of tree seedlings (trees with a diameter at breast
height <2.5 cm) with biomass (trees with a diameter at breast height > 2.5 cm) for sets of northern,
southern, and general tree species in the eastern United States using a spatially balanced, region-wide
forest inventory. Compared to mean latitude of tree biomass, mean latitude of seedlings was significantly
farther north (>20 km) for the northern study species, while southern species had no shift, and general
species demonstrated southern expansion. Density of seedlings relative to tree biomass of northern tree
species was nearly 10 times higher in northern latitudes compared to southern latitudes. For forest
inventory plots between 448 and 478 north latitude where southern tree species were identified, their
biomass averaged 0.46 tonnes/ha while their seedling counts averaged 2600 ha-1. It is hypothesized that
as northern and southern tree species together move northward due to greater regeneration success at
higher latitudes, general species may fill their vacated niches in southern locations. The results of this
study suggest that the process of northward tree migration in the eastern United States is currently
underway with rates approaching 100 km/century for many species.