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Nonetheless, molecular data support the hypothesis that terpenoid biosynthesis is modulated by C. herbacea herbivory.
Specifically, we address the following questions: (1) Do molecular data support the morphology-based field identification of Bruguiera × rhynchopetala?
Nearly all molecular data support a sister relationship between A. means and A. pholeter which diverged as recently as the late-Pliocene.
Previously described subspecies provide convenient (although not necessarily biologically meaningful) labels for most terminal haplogroups, however in six instances the molecular data support non-taxonomic groupings; namely in Angola, the Middle Zambezi Valley, the Luangwa Valley, Upper Volta, Lower Volta and Niger (Table S2).
Our molecular data support this assumption.
Both morphological and molecular data support a monophyly of Mantodea and Isoptera (see [ 25]).
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Finally, recent molecular data supports the formation of different co-adapted complexes between the Abd-B and Dsx proteins and its target genes.
Published molecular data supports the monophyly of these genera, i.e. [38] [40] showed that species assigned to Abyssogena, including phaseolifomis, kaikoi, and southwardae (from the Atlantic Ocean) form a well-supported cluster in a phylogenetic tree based on COI sequences.
Our best phylogenetic hypothesis (morphological + molecular data) supports most anomuran superfamilies and families as monophyletic.
The molecular data supports the historical species Group I-IV classification system for C. botulinum based upon biochemical and physical properties.
Furthermore, the molecular data supports a certain level of divergence between Clades B (in the north) and C (in the south).
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