Linking Restoration and Ecological Succession (Springer ... - Inecol
Linking Restoration and Ecological Succession (Springer ... - Inecol
Linking Restoration and Ecological Succession (Springer ... - Inecol
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Chapter 5 <strong>Succession</strong> <strong>and</strong> <strong>Restoration</strong> of Drained Fens 93<br />
of the energy, water, <strong>and</strong> matter budgets become more complex, the significance<br />
of storage grows, <strong>and</strong> consequently the residence times of inputs<br />
increase. Due to the high degree of mutual adaptation, the efficiencies of single<br />
transfer reactions rise, cycling is optimized, <strong>and</strong> thus losses of matter are<br />
reduced. The correlated ecosystem functions are usually investigated within<br />
three classes of processes:<br />
–Ecosystem energy balance: Exergy capture (uptake of usable energy) <strong>and</strong><br />
exergy storage (biomass, organic matter, <strong>and</strong> information) regularly increase<br />
during succession (Schneider <strong>and</strong> Kay 1994, Joergensen 2001). The<br />
total system throughput increases (Odum et al. 2000) <strong>and</strong> the energy dem<strong>and</strong><br />
for maintenance <strong>and</strong> respiration also increases (Svirezhev <strong>and</strong> Steinborn<br />
2001).<br />
–Ecosystem water balance: As terrestrial ecosystems <strong>and</strong> l<strong>and</strong>scapes develop<br />
without disturbance, more <strong>and</strong> more structural elements have to be<br />
supplied with water. Thus, water flows through vegetation compartments<br />
show a typical orientor behavior (optimization of biotic water flows, see<br />
Kutsch et al. 1998 <strong>and</strong> 2001). These fluxes are prerequisites for all cycling<br />
activities in terrestrial ecosystems. In this study, the hydrological features<br />
have been related to ecosystem productivity, hence representing a waterbased<br />
efficiency measure.<br />
–Ecosystem matter balance: During undisturbed ecosystem succession, imported<br />
nutrients are transferred throughout the biotic community with increased<br />
partitioning into more structures. Therefore, the biological nutrient<br />
fractions increase as well as the abiotic carbon <strong>and</strong> nutrient storages; the<br />
cycling rate also increases <strong>and</strong> efficiencies improve.<br />
5.2.2 Data Sets<br />
5.2.2.1 <strong>Succession</strong>al Models<br />
To describe retrogressive successional changes during l<strong>and</strong>-use intensification<br />
we use a model based on results of repeated vegetation mappings in fen areas<br />
of northern Germany (Schrautzer 1988). Secondary succession after ab<strong>and</strong>onment<br />
of fens uses the sequence described in the model of Jensen <strong>and</strong> Schrautzer<br />
(1999) that uses structural characteristics of the vegetation to define developmental<br />
stages. Most of the developmental stages have been studied on permanent<br />
plots or by repeated vegetation mapping. To assess the effect of rewetting<br />
on structure <strong>and</strong> processes of degenerated fens, we construct a successional<br />
sere that starts with intensively used wet pastures (Lolio-Potentillion), proceeds<br />
in time to eutrophic communities dominated by tall sedges <strong>and</strong> reeds<br />
(henceforth “tall sedge reeds,” Caricion elatae), <strong>and</strong> ends in the long run with<br />
eutrophic wet alder carrs (Alnion glutinosae). The retrogressive succession from<br />
wet alder carrs to wet pastures due to l<strong>and</strong>-use intensification, <strong>and</strong> the succession<br />
from wet meadows to dry alder carrs following ab<strong>and</strong>onment are shown<br />
in Fig. 5.1.<br />
5.2.2.2 Site Factors <strong>and</strong> Vegetation Parameters<br />
To characterize the site factors <strong>and</strong> productivities of the successional stages we<br />
used data from Schrautzer (2004), Schrautzer <strong>and</strong> Jensen (2006), <strong>and</strong> unpublished<br />
data. LAI (leaf area index) data were obtained from Schieferstein (1997),<br />
Trepel (2000), <strong>and</strong> Kutsch et al. (2000). Species richness (vascular plants) of