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Still, similar types of distributional changes have been documented for species in the more distant geological past.
Instead, we will focus on a time frame within which rapid behavioural and technological changes have been documented: the period between MIS 9 to 6.
However, such changes have been documented to have had significant effects on species' distributions and phylogenetic patterns in the distant geological past, for example, in the Cambrian and the Devonian (Lieberman and Eldredge 1996; Lieberman 2000b, 2003; Meert and Lieberman 2004; Rode and Lieberman 2005).
Similar changes have been documented for the H1 HA that caused the 1918 so-called Spanish influenza pandemic [19], [20].
Inconclusive central changes have been documented.
Additional transcript accumulation changes have been documented during seed development.
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Nonetheless, numerous instances of rapid morphological change have been documented.
While phenotypic responses to climate change have been documented (Bradshaw and Holzapfel 2006; Parmesan 2006; Hoffmann and Sgro 2011 and this issue), the potential for evolutionary rescue is still unclear (Bell 2013).
The reproducibility of this technique and the responsiveness to change have been documented elsewhere, 18 20 including one study using OAI data which demonstrated a responsiveness that compared favourably with MRI.
On the contrary, in recent years a decline in public concern and acceptance of climate change has been documented (Capstick and Pidgeon 2014).
While common means of measuring instructor learning via cognitive change has been documented for more experienced language instructors (cf. Borg, 2006) [1], graduate instructors are an often-overlooked population (cf. Gurzynski- Weiss, 2013; in press) [2] [3].
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