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Global Change Abstracts The Swiss Contribution - SCNAT

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94<br />

08.1-151<br />

Integrating environmental and economic<br />

performance to assess modern silvoarable<br />

agroforestry in Europe<br />

Palma J, Graves A R, Burgess P J, van der Werf W,<br />

Herzog F<br />

Switzerland, England, Netherlands<br />

Agriculture, Soil Sciences , Ecology , Biodiversity ,<br />

Economics<br />

<strong>The</strong> environmental and economic performance<br />

of silvoarable agroforestry in Europe is highly<br />

variable. Multi-criteria analysis, using the PRO-<br />

METHEE outranking approach, was used to evaluate<br />

the integrated performance of silvoarable<br />

agroforestry on hypothetical farms in nineteen<br />

landscape test sites in Spain, France, and <strong>The</strong><br />

Netherlands. <strong>The</strong> silvoarable scenarios allocated a<br />

proportion of the hypothetical farms (10 or 50%)<br />

to silvoarable agroforestry at two different tree<br />

densities (50 or 113 trees ha(-1)) on two different<br />

qualities of land (best or worst quality land). <strong>The</strong><br />

status quo (conventional arable farming) was also<br />

assessed for comparison. <strong>The</strong> criteria used in the<br />

evaluation (soil erosion, nitrogen leaching, carbon<br />

sequestration, landscape biodiversity, and<br />

infinite net present value) were assessed at each<br />

landscape test site; infinite net present value was<br />

assessed under six levels of government support.<br />

In France, the analysis showed, assuming equal<br />

weighting between environmental and economic<br />

performance, that silvoarable agroforestry was<br />

preferable to conventional arable farming. <strong>The</strong><br />

best results were observed when agroforestry was<br />

implemented on 50% of the highest quality land<br />

on the farm; the effect of tree density (50113 trees<br />

ha(-1)) was small. By contrast, in Spain and <strong>The</strong><br />

Netherlands, the consistently greater profitability<br />

of conventional arable agriculture relative to<br />

the agroforestry alternatives made overall performance<br />

of agroforestry systems dependent on the<br />

proportion of the farm planted, and the tree density<br />

and land quality used.<br />

Ecological Economics, 2007, V63, N4, SEP 15, pp<br />

759-767.<br />

08.1-152<br />

<strong>The</strong> odd man out? Might climate explain the<br />

lower tree alpha-diversity of African rain forests<br />

relative to Amazonian rain forests?<br />

Parmentier I, Malhi Y, Senterre B, Whittaker R J,<br />

Alonso A, Balinga M P B, Bakayoko A, Bongers<br />

F, Chatelain C, Comiskey J A, Cortay R, Kamdem<br />

M N D, Doucet J L, Gautier L, Hawthorne W D,<br />

Issembe Y A, Kouame F N, Kouka L A, Leal M E,<br />

Lejoly J, Lewis S L, Nusbaumer L, Parren M P E, Peh<br />

K S H, Phillips O L, Sheil D, Sonke B, Sosef M S M,<br />

<strong>Global</strong> <strong>Change</strong> <strong>Abstracts</strong> – <strong>The</strong> <strong>Swiss</strong> <strong>Contribution</strong> | Terrestrial Ecosystems<br />

Sunderland T C H, Stropp J, Ter Steege H, Swaine<br />

M D, Tchouto M G P, van Gemerden Barend S, van<br />

Valkenburg J L C H, Wöll H<br />

Belgium, England, USA, Cameroon, Cote Ivoire,<br />

Switzerland, Gabon, Ghana, Indonesia, Netherlands,<br />

Scotland<br />

Meteorology & Atmospheric Sciences , Forestry ,<br />

Plant Sciences , Ecology , Biodiversity<br />

1. Comparative analyses of diversity variation<br />

among and between regions allow testing of alternative<br />

explanatory models and ideas. Here, we<br />

explore the relationships between the tree alphadiversity<br />

of small rain forest plots in Africa and<br />

in Amazonia and climatic variables, to test the<br />

explanatory power of climate and the consistency<br />

of relationships between the two continents. 2.<br />

Our analysis included 1003 African plots and 512<br />

Amazonian plots. All are located in old-growth primary<br />

non-flooded forest under 900 m altitude. Tree<br />

alpha-diversity is estimated using Fisher’s alpha calculated<br />

for trees with diameter at breast height >=<br />

10 cm. Mean diversity values are lower in Africa by a<br />

factor of two. 3. Climate-diversity analyses are based<br />

on data aggregated for grid cells of 2.5 x 2.5 km. <strong>The</strong><br />

highest Fisher’s alpha values are found in Amazonian<br />

forests with no climatic analogue in our African<br />

data set. When the analysis is restricted to pixels of<br />

directly comparable climate, the mean diversity of<br />

African forests is still much lower than that in Amazonia.<br />

Only in regions of low mean annual rainfall<br />

and temperature is mean diversity in African forests<br />

comparable with, or superior to, the diversity in<br />

Amazonia. 4. <strong>The</strong> climatic variables best correlated<br />

with the tree alpha- diversity are largely different<br />

in the African and Amazonian data, or correlate<br />

with African and Amazonian diversity in opposite<br />

directions. 5. <strong>The</strong>se differences in the relationship<br />

between local/landscape- scale alpha-diversity and<br />

climate variables between the two continents point<br />

to the possible significance of an array of factors<br />

including: macro-scale climate differences between<br />

the two regions, overall size of the respective species<br />

pools, past climate variation, other forms of<br />

long-term and short-term environmental variation,<br />

and edaphics. We speculate that the lower alpha-diversity<br />

of African lowland rain forests reported here<br />

may be in part a function of the smaller regional<br />

species pool of tree species adapted to warm, wet<br />

conditions. 6. Our results point to the importance<br />

of controlling for variation in plot size and for gross<br />

differences in regional climates when undertaking<br />

comparative analyses between regions of how local<br />

diversity of forest varies in relation to other putative<br />

controlling factors.<br />

Journal of Ecology, 2007, V95, N5, SEP, pp<br />

1058-1071.

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