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Pollen morphology of the tribe Rhinantheae (Orobanchaceae) and its systematic significances

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Abstract

Pollen morphology of 36 species representing 14 genera within the tribe Rhinantheae in the family Orobanchaceae was studied and illustrated with light microscopy (LM) and scanning electron microscopy (SEM). Five major pollen types were recognized on the basis of exine ornamentation. Within these major types, minor types (subtypes) were distinguished based on exine surface pattern, size, shape, amb form, colpi and colpus membrane. These types and subtypes are as follows: type I. retipilate: subtype Ia. regular retipilate: (1) pollen size < 27 µm, (2) pollen size > 27 µm, subtype Ib. irregular retipilate; type II. verrucate: subtype IIa. macro-verrucate, subtype IIb. verrucate, subtype IIc. sparse verrucate; type III. retirugulate; type IV. granulate; type V. micro-reticulate. A key to pollen morphology of genera studied within the Rhinantheae was made based on pollen morphology from our study and earlier work. Combining with other sources of information on the Rhinantheae, the systematic relationships of this tribe are discussed. Rhinantheae pollen displays considerable variation between genera and species, with taxonomically significant characters at genus and species level. Palynological characteristics provide evidence for interpreting the conflicting views concerning the “Pterygiella Complex”. The evolutionary trend in exine sculpture of Rhinantheae could be proposed, namely that retipilate sculpturing which is the most widespread type is more primitive than the other types (such as foveolate, granulate, regulate, reticulate, retirugulate and verrucate). The pollen data in present study and the view of Hong (1986), as well as the molecular data from Bennett and Mathews (2006) indicated that Asia and related regions were likely to the origin centre of the tribe Rhinantheae.

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Lu, L., Wang, H., Blackmore, S. et al. Pollen morphology of the tribe Rhinantheae (Orobanchaceae) and its systematic significances. Plant Syst. Evol. 268, 177–198 (2007). https://doi.org/10.1007/s00606-007-0562-x

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