Johnson et al. (2004) described another common expression of maladaptation

which appeared years after planting. In their example, Pseudotsuga menziesii provenances introduced into RGFP966 cell line Oregon, USA, performed well from 1915 to 1955 and then were hit with an unusual and prolonged cold period; local sources survived but off-site sources were either badly damaged or killed. Similarly, 30,000 ha of Pinus pinaster Aiton plantations, established in the Landes region of France with non-frost-resistant material from the Iberian Peninsula, were destroyed during the bad winter of 1984 into 1985 ( Timbal et al., 2005). Since the first generation of trees plays a key role in subsequent natural regeneration at a site, if the founder population is established using FRM from a small number of related trees, the consequent low genetic diversity and inbreeding may result in reduced fitness in future generations (McKay et al., 2005, Reed and Frankham,

2003 and Stacy, 2001). In particular, if the original planting material is vegetatively propagated and originates from just Tyrosine Kinase Inhibitor Library purchase a few trees, self-pollination can be a problem in the next generation. In a study which compared selfed and outcrossed offspring of clonal Pseudotsuga menziesii 33 years after establishment, for example, the average survival of selfed offspring was only 39% of that of the outcrossed trees. Moreover, the average diameter at breast height of the surviving selfed trees was only 59% that of the surviving outcrossed trees ( White et al., 2007). When planting material originates from seed collected from a few related trees, inbreeding effects will be less serious, but depending on the amount of mating

between close relatives, fitness may be reduced in subsequent generations. Ensuring a minimum level of genetic diversity in founder populations Carbohydrate is particularly important in restoration projects, considering that regardless of breeding system, inbreeding depression is more commonly expressed in more stressful environments ( Fox and Reed, 2010), such as the degraded soils found at most restoration sites. There is a general preference in ecosystem restoration efforts for FRM from local sources (Breed et al., 2013, McKay et al., 2005 and Sgrò et al., 2011). This is based on the assumption that local FRM has undergone natural selection to become best adapted to the local conditions of a nearby restoration site, an assumption that is not always correct (Bischoff et al., 2010, Hereford, 2009, Kettenring et al., 2014 and McKay et al., 2005). Local adaptation may, for example, be hindered by gene flow, genetic drift, and/or a lack of genetic variation. The superiority of non-local genotypes has been demonstrated in reciprocal transplant experiments for some herbaceous plant species (Bischoff et al., 2010), and through provenance trials of some tree species (e.g., Cordia alliodora).