In the degraded soils that typify restoration sites, conditions may be very different from those under which local populations Venetoclax in vitro originally developed. Environmental mosaics may result in sites far apart having similar ecologies, while closer sites differ. Where remaining forests near the restoration area are highly fragmented,
isolated trees may be inbred, have reduced fitness, or exhibit other negative consequences of small population size, and may not constitute good seed sources (Aguilar et al., 2008, Breed et al., 2012, Eckert et al., 2010, Honnay et al., 2005, Lowe et al., 2005, Szulkin et al., 2010 and Vranckx et al., 2012). These conditions can be assumed to be common in many areas where restoration efforts are targeted. The quality of existing local forest patches as sources of FRM must also be carefully evaluated in the light of past or ongoing resource use or disturbance, particularly silvicultural management practices (Lowe et al., 2005, Schaberg et al., 2008, Soldati et al., 2013 and Wickneswari et al., 2004). For example, the high intensity of some logging methods may modify breeding patterns in the residual trees and result in increasingly inbred seeds through selfing or crossing between closely check details related individuals (Ghazoul et al., 1998, Murawski et al., 1994, Ng et al., 2009 and Wickneswari et al.,
2014), compromising the population as a seed source. In such cases, sourcing FRM from further away,
yet from similar ecological conditions, may be a better option than resorting to nearby fragmented or intensively logged forests or isolated trees (Breed et al., 2011 and Sgrò et al., 2011). Any introduction of non-local FRM, even of native species, holds risks. If the non-local FRM is of the same species, or closely related to the species remaining on the restoration site, but from genetically distinct sources, Beta adrenergic receptor kinase there is a risk of genetic contamination of the local populations (Ellstrand and Schierenbeck, 2000, Rogers and Montalvo, 2004, McKay et al., 2005 and Millar et al., 2012). Therefore, it is important to try to ensure that FRM is genetically matched to the neighbouring (fragmented) populations of the same species (McKay et al., 2005 and Aitken et al., 2008). Gene flow between native resident populations and non-local introduced plants might lead to outbreeding depression. Outbreeding depression occurs when crosses between local and non-local sources produce generations with reduced fitness (Lowe et al., 2005). One theory to explain the occurrence of outbreeding depression is that co-adapted gene complexes are broken up during recombination (Templeton, 1986). Outbreeding depression is widely discussed, although there is still little hard evidence for or against it in trees (but see Stacy, 2001 and Frankham et al., 2011).
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