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We analyzed diversity of pollen transported by pollinators and the pollination niche overlap among plants in both types of fragments with general and generalized linear mixed models.
For instance, fragments of horizontal stems of giant reed (Arundo donax) had a higher sprouting ability than fragments of vertical stems when both types of fragments were positioned horizontally [15], [16], and this was related to differences in the distributions of auxins in the fragments.
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In the surrounding areas of both types of implants, bone fragments were noticed around the implant.
In both types of farms, forest fragments required some degree of restoration.
Based on the types of fragments observed and fragmentation patterns found, we propose detailed mechanisms for protein backbone cleavage and side chain dissociation in EDD.
Both types of libraries contain sequenced genomic fragments that are effectively randomly distributed throughout the genome; however, they differ in being comprised of actively transcribed components only in the case of EST libraries versus random genomic fragments in the case of BAC libraries.
We define two types of fragments, rigid moieties and flexible linkers; each unique fragment is accompanied by the connectivity information.
Table 4 lists the spatial extent of various types of fragments (interior, perforated, edge, transitional and patch forests).
Fig. 4 The scaled distributions of molecular weight for nine types of fragments found in the 12 datasets.
Our fragment approach differs, however, in using different types of fragments, as well as by a different method to calculate fragment contributions.
Fig. 1 Definitions of different types of fragments in a molecule: a ring systems, b linkers, c side chains and d Murcko framework, e ring assemblies, f bridge assemblies, g rings, h RECAP fragments and i scaffold tree.
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