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LCA Food 2012 in Saint Malo, France! - Manifestations et colloques ...

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PLENARY SESSION 3: METHODS FOR BIODIVERSITY AND SOIL QUALITY 8 th Int. Conference on <strong>LCA</strong> <strong>in</strong> the<br />

Agri-<strong>Food</strong> Sector, 1-4 Oct <strong>2012</strong><br />

2. M<strong>et</strong>hods<br />

We calculated land use impacts on biodiversity accord<strong>in</strong>g the UNEP/SETAC Life Cycle Initiative<br />

Framework (Koellner <strong>et</strong> al., <strong>2012</strong>a; Milà i Canals <strong>et</strong> al., 2007), and dist<strong>in</strong>guished b<strong>et</strong>ween occupation (land<br />

use), transformation (land use change) and permanent impacts (irreversible changes <strong>in</strong> ecosystems, see Fig<br />

1). Occupation and transformation impacts were calculated based on regional ext<strong>in</strong>ction risk of non-endemic<br />

species. Permanent impacts were based on the ext<strong>in</strong>ction risk of species endemic to that ecoregion. Below,<br />

we outl<strong>in</strong>e how the number of potentially ext<strong>in</strong>ct species was estimated and how we derived regional characterisation<br />

factors for the three land use impacts (occupation, transformation, and permanent impacts).<br />

Figure 1. Graphical illustration of occupation, transformation and permanent impacts (adapted from Koellner<br />

<strong>et</strong> al., <strong>2012</strong>a)<br />

2.1 Calculat<strong>in</strong>g potential regional mammal species ext<strong>in</strong>ctions due to land transformation and occupation<br />

As <strong>in</strong> earlier land use LCIA studies, we based our assessment on changes <strong>in</strong> the predicted species numbers<br />

accord<strong>in</strong>g to the species-area relationship (SAR), a model often used to predict ext<strong>in</strong>ction rates due to<br />

habitat loss. The SAR is derived from island biogeography theory, which describes a non-l<strong>in</strong>ear (often<br />

power) function b<strong>et</strong>ween species richness S and area A of island ecosystems (Rosenzweig 1995):<br />

S= cA Eq. 1<br />

with two constants c (species richness of area A=1) and z (species accumulation rate). If the area of primary<br />

habitat is reduced from an orig<strong>in</strong>al area to an area , and if we assume , then the<br />

relative number of species S rema<strong>in</strong><strong>in</strong>g can be calculated as (Koh and Ghazoul 2010):<br />

z<br />

A A c org new new = corg z<br />

Snew Sorg =<br />

Eq. 2<br />

The number of species lost <strong>in</strong> an ecosystem due to habitat loss is given as (Koh and Ghazoul 2010):<br />

A æ ö<br />

new<br />

ç<br />

è A<br />

÷<br />

org ø<br />

æ A ö<br />

new<br />

Slost = Sorg - Sorg ç<br />

A<br />

÷<br />

è org ø<br />

Eq. 3<br />

As SAR models tend to overestimate ext<strong>in</strong>ction rates, we base our m<strong>et</strong>hod on an adapted SAR model, the<br />

matrix-SAR developed by Koh and Ghazoul (2010), which gave more realistic estimates of species ext<strong>in</strong>ction<br />

rates than the conventional SAR model. Unlike the conventional SAR, the matrix-SAR model considers<br />

that the human-modified area (i.e. the land use matrix) is not void of species, but provides a certa<strong>in</strong> habitat<br />

quality for different species groups. This is accounted for by adapt<strong>in</strong>g z, the exponent of Eq. 3, depend<strong>in</strong>g on<br />

the composition of the matrix (i.e. the area share of different land use types pi) and the sensitivity of each<br />

taxonomic group to different land use types i (Koh and Ghazoul 2010):<br />

å<br />

n<br />

z<br />

S lost<br />

z ¢ = z* pis i ; with Eq. 4<br />

i<br />

A i<br />

pi =<br />

Aorg - Anew s i<br />

Eq. 5<br />

341

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