User:Annikals/Nectar spur (flower)

Nectar spur

Side view of Tropaeolum majus, a plant with a nectar spur arising from the hypanthium of the flower. A nectar spur is a hollow extension of a part of a flower. The spur may arise from various parts of the flower: the sepals, petals, or hypanthium. Spurs often contain tissues that secrete nectar (nectaries), but can also function as a receptacle for nectar drained from a nectary outside of the flower. Nectar spurs are associated with coevolution with pollinators such as hummmingbirds, moths, and bees.

Functional significance of nectar spurs

The long tongue of a sphinx moth is depicted as reaching into the equally long-spurred orchid. Spur length can be an important diagnostic character for taxonomy, but it can also play a functional role in the ecology of the flower. The length of nectar spurs varies, and is generally correlated with the lengths of the tongues of their major pollinators. can restrict access of pollinators to nectar, limiting the range of potential pollinators. In a famous historical story, Darwin predicted the that that Angraecum sesquipedale, an orchid with an extremely long spur, must be pollinated by a pollinator an equally long tongue. The pollinator, the sphinx moth Xanthopan morgani ssp. praedicta with a 22 cm tongue, was found 40 years after Darwin made his prediction.

The spur can also aid in consistent placement of pollen on the pollinator, functionally positioning the pollinator so that its contact with the anthers/stigmas is more controlled.

Nectar Spurs and Evolution Nectar spurs have been cited as prime examples of “key innovations” that may promote diversification, and play a part in the adaptive radiation of clades. Columbines (Aquilegia) have been studied in depth for the link between their floral nectar spurs and their rapid evolutionary radiations. However, there has also been some refutation to this idea recently, suggesting that the adaptive radiation of Aquilegia may have been due more to climate and habit.

Underlying Development and Genetics In terms of development, the varying lengths of nectar spurs has been found to be based solely on the anisotropic elongation of cells.

The genetic basis underlying the development of nectar spurs has been explored in several clades of plant families, such as Linaria and Aquilegia. Studies in model plant Antirrhinum identified KNOX genes in spur development, which gene expression studies confirmed in Linaria. However, the same genes were not expressed during spur development in Aquilegia, suggesting a case of convergent evolution, where the nectar spur has developed through different developmental pathways.

List of plants with nectar spurs: Orchids: (Satyrium, Disa)

On petals: Aquilegia, Lentibulariaceae, Viola, Fumarioideae

On sepals: Delphinium, Impatiens

From hypanthium: Tropaeolum

Notes Heerema, R. J.; Weinbaum, S. A.; Pernice, F.; Dejong, T. M. (2008-01-01). "Spur survival and return bloom in almond [Prunus dulcis (Mill.) D.A.Webb] varied with spur fruit load, specific leaf weight, and leaf area". The Journal of Horticultural Science and Biotechnology. 83 (2): 274–281. doi:10.1080/14620316.2008.11512380. ISSN 1462-0316. Whittall, Justen B.; Hodges, Scott A. "Pollinator shifts drive increasingly long nectar spurs in columbine flowers". Nature. 447 (7145): 706–709. doi:10.1038/nature05857. Hodges, Scott A. (1997). "Floral Nectar Spurs and Diversification". International Journal of Plant Sciences. 158. No. 6, Supplement: Morphology and Evolution of Flowers: S81–S88 – via JSTOR. Bastida, Jesús M.; Alcántara, Julio M.; Rey, Pedro J.; Vargas, Pablo; Herrera, Carlos M. (2009-12-04). "Extended phylogeny of Aquilegia: the biogeographical and ecological patterns of two simultaneous but contrasting radiations". Plant Systematics and Evolution. 284 (3-4): 171–185. doi:10.1007/s00606-009-0243-z. ISSN 0378-2697. Donoghue, Michael J.; Sanderson, Michael J. (2015-07-01). "Confluence, synnovation, and depauperons in plant diversification". New Phytologist. 207 (2): 260–274. doi:10.1111/nph.13367. ISSN 1469-8137. Fior, Simone; Li, Mingai; Oxelman, Bengt; Viola, Roberto; Hodges, Scott A.; Ometto, Lino; Varotto, Claudio (2013-04-01). "Spatiotemporal reconstruction of the Aquilegia rapid radiation through next-generation sequencing of rapidly evolving cpDNA regions". New Phytologist. 198 (2): 579–592. doi:10.1111/nph.12163. ISSN 1469-8137. Puzey, Joshua R.; Gerbode, Sharon J.; Hodges, Scott A.; Kramer, Elena M.; Mahadevan, L. (2012-04-22). "Evolution of spur-length diversity in Aquilegia petals is achieved solely through cell-shape anisotropy". Proceedings of the Royal Society of London B: Biological Sciences. 279 (1733): 1640–1645. doi:10.1098/rspb.2011.1873. ISSN 0962-8452. PMC PMC3282339 Check |pmc= value (help). . Glover, Beverley J.; Airoldi, Chiara A.; Brockington, Samuel F.; Fernández-Mazuecos, Mario; Martínez-Pérez, Cecilia; Mellers, Greg; Moyroud, Edwige; Taylor, Lin (2015-05-01). "How Have Advances in Comparative Floral Development Influenced Our Understanding of Floral Evolution?". International Journal of Plant Sciences. 176 (4): 307–323. doi:10.1086/681562. ISSN 1058-5893. Travers, Steven E; Temeles, Ethan J; Pan, Irvin (2003-02-01). "The relationship between nectar spur curvature in jewelweed (Impatiens capensis) and pollen removal by hummingbird pollinators". Canadian Journal of Botany. 81 (2): 164–170. doi:10.1139/b03-014. ISSN 0008-4026. Ronse Decraene, L (2001-11-01). "Floral Developmental Evidence for the Systematic Relationships of Tropaeolum(Tropaeolaceae)". Annals of Botany. 88 (5): 879–892. doi:10.1006/anbo.2001.1525. ISSN 0305-7364.