Literature DB >> 20053630

On the mechanisms of nectar secretion: revisited.

A E Vassilyev1.   

Abstract

BACKGROUND AND SCOPE: Models of nectar formation and exudation in multilayered nectaries with modified stomata or permeable cuticle are evaluated. In the current symplasmic model the pre-nectar moves from terminal phloem through the symplasm into the apoplasm (cell walls and intercellular spaces) with nectar formation by either granulocrine or eccrine secretion and its diffusion outwards. It is concluded, however, that no secretory granules are actually produced by the endoplasmic reticulum, and that secretory Golgi vesicles are not involved in the transport of nectar sugar. Therefore, the concept of granulocrine secretion of nectar should be discarded. The specific function of the endomembrane system in nectary cells remains unknown. According to the apoplasmic model, the pre-nectar moves from the terminal phloem in the apoplasm and, on the way, is transformed from phloem sap into nectar. However, viewed ultrastructurally, the unloading (terminal) phloem of nectaries appears to be less active than that of the leaf minor veins, and is therefore not actively involved in the secretion of pre-nectar components into the apoplasm. This invalidates the apoplasmic model. Neither model provides an explanation for the origin of the driving force for nectar discharge. PROPOSAL: A new model is proposed in which nectar moves by a pressure-driven mass flow in the nectary apoplasm while pre-nectar sugars diffuse from the sieve tubes through the symplasm to the secretory cells, where nectar is formed and sugars cross the plasma membrane by active transport ('eccrine secretion'). The pressure originates as the result of water influx in the apoplasm from the symplasm along the sugar concentration gradient. It follows from this model that there can be no combinations of apoplasmic and symplasmic pre-nectar movements. The mass-flow mechanism of nectar exudation appears to be universal and applicable to all nectaries irrespective of their type, morphology and anatomy, presence or absence of modified stomata, and their own vascular system.

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Year:  2010        PMID: 20053630      PMCID: PMC2826252          DOI: 10.1093/aob/mcp302

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  4 in total

Review 1.  Traffic between the plant endoplasmic reticulum and Golgi apparatus: to the Golgi and beyond.

Authors:  Loren A Matheson; Sally L Hanton; Federica Brandizzi
Journal:  Curr Opin Plant Biol       Date:  2006-09-28       Impact factor: 7.834

2.  Ultrastructural evidence for a dual function of the phloem and programmed cell death in the floral nectary of Digitalis purpurea.

Authors:  Karl Peter Gaffal; Gudrun Johanna Friedrichs; Stefan El-Gammal
Journal:  Ann Bot       Date:  2007-02-13       Impact factor: 4.357

3.  Nectar production and transportation in the nectaries of the female Cucumis sativus L. flower during anthesis.

Authors:  Yi-Ben Peng; Yi-Qin Li; Yu-Jin Hao; Zhi-Hong Xu; Shu-Nong Bai
Journal:  Protoplasma       Date:  2004-10       Impact factor: 3.356

4.  Floral nectar production and nectary anatomy and ultrastructure of Echinacea purpurea (Asteraceae).

Authors:  Tyler J Wist; Arthur R Davis
Journal:  Ann Bot       Date:  2005-12-09       Impact factor: 4.357

  4 in total
  19 in total

1.  Micromorphology and ultrastructure of the floral nectaries of Polemonium caeruleum L. (Polemoniaceae).

Authors:  Mirosława Chwil; Stanisław Chwil
Journal:  Protoplasma       Date:  2011-10-28       Impact factor: 3.356

Review 2.  How do secretory products cross the plant cell wall to be released? A new hypothesis involving cyclic mechanical actions of the protoplast.

Authors:  Elder Antônio Sousa Paiva
Journal:  Ann Bot       Date:  2016-02-29       Impact factor: 4.357

3.  Extrafloral nectaries of four varieties of Chamaecrista ramosa (Vogel) H.S.Irwin & Barneby (Fabaceae): anatomy, chemical nature, mechanisms of nectar secretion, and elimination.

Authors:  Priscila da Silva Pereira; Letícia de Almeida Gonçalves; Marcos José da Silva; Maria Helena Rezende
Journal:  Protoplasma       Date:  2018-04-27       Impact factor: 3.356

4.  Microstructure of floral nectaries in Robinia viscosa var. hartwigii (Papilionoideae, Fabaceae)-a valuable but little-known melliferous plant.

Authors:  Agata Konarska
Journal:  Protoplasma       Date:  2019-11-17       Impact factor: 3.356

5.  Upper-limit agricultural dietary exposure to streptomycin in the laboratory reduces learning and foraging in bumblebees.

Authors:  Laura Avila; Elizabeth Dunne; David Hofmann; Berry J Brosi
Journal:  Proc Biol Sci       Date:  2022-02-09       Impact factor: 5.349

6.  Understanding ontogenetic trajectories of indirect defence: ecological and anatomical constraints in the production of extrafloral nectaries.

Authors:  Nora Villamil; Judith Márquez-Guzmán; Karina Boege
Journal:  Ann Bot       Date:  2013-02-03       Impact factor: 4.357

7.  Structure of floral nectaries and female-biased nectar production in protandrous species Geranium macrorrhizum and Geranium phaeum.

Authors:  Agata Konarska; Marzena Masierowska
Journal:  Protoplasma       Date:  2019-12-02       Impact factor: 3.356

8.  Poplar extrafloral nectaries: two types, two strategies of indirect defenses against herbivores.

Authors:  María Escalante-Pérez; Mario Jaborsky; Silke Lautner; Jörg Fromm; Tobias Müller; Marcus Dittrich; Maritta Kunert; Wilhelm Boland; Rainer Hedrich; Peter Ache
Journal:  Plant Physiol       Date:  2012-05-09       Impact factor: 8.340

9.  Comparative floral spur anatomy and nectar secretion in four representatives of Ranunculaceae.

Authors:  Sebastian Antoń; Magdalena Kamińska
Journal:  Protoplasma       Date:  2015-03-15       Impact factor: 3.356

10.  Flexible resource allocation during plant defense responses.

Authors:  Jack C Schultz; Heidi M Appel; Abigail P Ferrieri; Thomas M Arnold
Journal:  Front Plant Sci       Date:  2013-08-22       Impact factor: 5.753

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