Megaherbs are a group of herbaceous wildflowers growing in the New Zealand subantarctic islands and on the other subantarctic islands. They are characterised by their great size, with huge leaves and very large and often unusually coloured flowers, which have evolved as an adaptation to the harsh weather conditions on the islands. They suffer from overgrazing due to introduced mammals.

Megaherbs on Campbell Island

Appearance and occurrence edit

 
Close-up on megaherbs on Enderby Island

Originally, the term was coined to describe large-leaved herbs that form meadows in the subantarctic islands[1] but has also been applied to describe tropical alpine vegetation forms[2] found in the Andes, East Africa and New Guinea.[3] They are large herbs that can reach dimensions of over one metre, often feature strikingly colourful flowers,[4][5] large leaves and long stalks,[6] and are important components of the ecosystems of the subantarctic islands.[7] Beyond these traits, megaherbs can have different forms;[8] for example, some genera have perennial leaves and others are deciduous.[9] Intensely coloured flowers are not unique to megaherbs but also occur on other plant species in the same environments[10] and either arose by chance or are evolutionary adaptations to the environment.[11]

They live in the wet, windy and cold environments of the subantarctic islands, where they coexist with cushion plants and tussock grasses but trees are absent. A single species, Pleurophyllum hookeri, covers almost a third of Macquarie Island[12] where another megaherb, Stilbocarpa polaris, also occurs.[13] They reach their maximum extent on that island.[14] The only subantarctic islands lacking them are the Falklands and South Georgia, but Poa flabellata on South Georgia could be considered a megaherb.[15] Typical settings are water-rich with fertile soils; sometimes they are associated with volcanic heat sources.[16] On Campbell Island they appear to occur preferentially in nutrient-rich (eutrophic) terrain. Researchers since the 1940s often incorrectly assumed that they are limited to cliffs and ledges, as grazers had extirpated them from other areas.[17]

The most extraordinary of the megaherbs is the Pleurophyllum meadow, a community dominated by the large-leafed herbaceous composite, producing a floral display second to none outside the tropics

— Joseph Dalton Hooker, quoted in Fell, 2002[1]

They are the best known plants of the New Zealand subantarctic islands[18] and are important components of the biodiversity of the region.[2] Another name is "megaphyllous herbs".[3]

Taxa edit

Common taxa forming megaherbs are Asteraceae, Apiaceae, Araliaceae, Asphodelaceae, Asteraceae, Boraginaceae, Brassicaceae, Gentianaceae and Liliaceae; sometimes Poaceae (grasses) are also included.[15][19] In the New Zealand subantarctic islands, four endemic genera make up megaherbs. Among these are Anisotome and Bulbinella with colourful flowers and Pleurophyllum and Stilbocarpa with large leaves.[18][20] Additional genera are Gentianella[21] and Pringlea.[7]

Note megaherb species are the Campbell Island carrot (Anisotome latifolia) and the Ross lily (Bulbinella rossii).[22] The Chatham Island forget-me-not (Myosotidium hortensia) naturally occurs on the Chatham Islands but has been brought to New Zealand. It has large leaves and forms rosettes up to one metre wide.[23] The Kerguelen cabbage (Pringlea antiscorbutica) is a megaherb species that occurs on Heard Island where it is a key species in herbfields, Iles Crozet, Iles Kerguelen, Marion Island and Prince Edward Island.[24]

Other species called "megaherbs" include Phormium colensoi on New Zealand.[25] The Mountain buttercup (Ranunculus lyallii) is also considered a megaherb[26] and Astelia solani has been referred to as one.[27] The species Aciphylla latifolia, Bulbinella rossii, Myosotidium hortensia, Pleurophyllum spp. and Stilbocarpa in the Chatham Islands have been referred to as "macrophyllous forbs".[28] Finally, Angelica archangelica in Iceland has been considered an example of a Northern Hemisphere megaherb.[15]

Evolutionary history and ecology edit

The origins of the megaherb growth form are enigmatic. Several different subantarctic genera independently evolved this trait, which is defining for the genus Pleurophyllum.[20] Stilbocarpa megaherbs evolved from ancestors with smaller leaves.[29] These plants survived the last glacial maximum on the subantarctic islands and spread northward after its end.[30] Related species also occur on New Zealand.[31]

Megaherbs have been described as a form of gigantism.[21] The evolution of the megaherb form may be a consequence of specific conditions in the subantarctic islands.[20][4] The large leaves could be intercepting nutrient-bearing aerosols and trap heat in cold environments. Rosette growths reduce wind speeds and wind-driven evaporation and cooling.[31] The leaves may also act to absorb heat from diffuse radiation[17] and higher temperatures have been measured in megaherbs than the surrounding environment.[32] At the same time, the lack of herbivores, plentiful water and nutrients brought by e.g seabirds and steady temperatures facilitate the growth of large plants.[29][15] On Adams Island megaherbs are well developed where they are fertilized by guano. In return, birds use them as cover and source of insects[33] and are burrowed by nesting birds.[34] Such burrowing may influence the establishment of megaherb communities.[35] They are among the first plants to resettle former albatross nests on Adams Island.[36] The simultaneous occurrence of large leaves, large underground storage tissues, large seeds and large seed output is also found in megaherbs and appears to reflect unusual adaptations, as resource trade-off would normally prohibit their simultaneous occurrence.[7]

Herbs with large leaves occur in other places such as Chile, Hawaii, Kenya and New Zealand but there are traits specific for subantarctic megaherbs[37][30] and there are environmental differences, such as lower and more steady insolation.[38] Their evolution may be driven by similar environmental factors that are encountered on high mountains and in polar climates,[29] such as cold and windy weather, and may thus be examples of convergent evolution.[39]

Wētā, flightless crickets of New Zealand, have been observed to pollinate megaherbs and may constitute their main pollinators.[40] Moths have also been observed pollinating megaherbs.[41]

Human history edit

Megaherbs were first described by the British botanist Joseph Dalton Hooker, who coined the term in 1847.[1] Megaherbs draw the interest of scientists and tourists alike;[16] they are the main claim to fame of Campbell Island for example.[42] The Fairchilds Garden site on Adams Island was noted already in 1891 for its megaherbs.[33] The characteristic appearance makes Pleurophyllum a plant that could be used in horticulture, but attempts to cultivate it outside of the subantarctic environment have largely been unsuccessful.[20]

Threats edit

Megaherbs are susceptible to overgrazing by mammals.[17] Feral pigs have devastated megaherb communities on Auckland Island.[43] On Macquarie Island, rabbits consume megaherbs while rats cache seeds of Pleurophyllum hookeri[44] in places unsuited for their germination,[45] and the growth of the rabbit population has resulted in a major reduction of megaherb populations, as well as of other plant taxa of the island.[46]

Where grazing animals have been removed, megaherb species often quickly reoccupy the terrain.[31] This is expected to occur on Macquarie Island after rabbit and rodent populations[47] began to shrink since 2010. They will probably displace less edible but also less competitive plant species like Agrostis magellanica and Acaena magellanica.[44] Conversely only a partial recovery took place on Campbell Island by 1994.[48]

Other uses of the term edit

The term "megaherb" is sometimes used to describe plant species from other continents that have features similar to subantarctic megaherbs.[49] It has also been used to describe members of the family Heliconiaceae, which are tropical species,[50] and for the Amazonian species Phenakospermum guyannense.[51]

Gallery edit

See also edit

References edit

  1. ^ a b c Wagstaff, Breitwieser & Ito 2011, p. 63.
  2. ^ a b Shaw, Hovenden & Bergstrom 2005, p. 118.
  3. ^ a b Mark, Dickinson & Hofstede 2000, p. 251.
  4. ^ a b Komai & Emura 1955, p. 87.
  5. ^ MEURK, FOGGO & WILSON 1994, p. 161.
  6. ^ Panagiotakopulu & Sadler 2021, p. 125.
  7. ^ a b c Convey, P.; Chown, S. L.; Wasley, J.; Bergstrom, D. M. (2006). "Life History Traits". Trends in Antarctic Terrestrial and Limnetic Ecosystems: Antarctica as a Global Indicator. Springer Netherlands. p. 107. doi:10.1007/1-4020-5277-4_6. ISBN 978-1-4020-5277-4.
  8. ^ Saldivia et al. 2022, pp. 615–616.
  9. ^ Wagstaff, Breitwieser & Ito 2011, p. 71.
  10. ^ Lord et al. 2013, p. 169.
  11. ^ Lord et al. 2013, p. 170.
  12. ^ Briggs, Selkirk & Bergstrom 2006, p. 187.
  13. ^ Briggs, Selkirk & Bergstrom 2006, p. 188.
  14. ^ Fernández-Palacios, José María (2009). Encyclopedia of islands. Berkeley: University of California Press. p. 574. ISBN 9780520943728.
  15. ^ a b c d Panagiotakopulu & Sadler 2021, p. 126.
  16. ^ a b Mucina 2023, p. 141.
  17. ^ a b c MEURK, FOGGO & WILSON 1994, p. 162.
  18. ^ a b "Plants on New Zealand's subantarctic islands". Department of Conservation. New Zealand Government. Retrieved 21 June 2021.
  19. ^ Mucina 2023, p. 142.
  20. ^ a b c d Wagstaff, Breitwieser & Ito 2011, p. 70.
  21. ^ a b Wallis, Graham P.; Trewick, Steven A. (2009). "New Zealand phylogeography: evolution on a small continent". Molecular Ecology. 18 (17): 3552. doi:10.1111/j.1365-294X.2009.04294.x. ISSN 1365-294X. PMID 19674312.
  22. ^ Mucina 2023, p. 136.
  23. ^ "Chatham Island forget-me-not". Department of Conservation (New Zealand). New Zealand Government. Retrieved 21 June 2021.
  24. ^ Schortemeyer, Marcus; Evans, John R.; Bruhn, Dan; Bergstrom, Dana M.; Ball, Marilyn C. (2015-04-17). "Temperature responses of photosynthesis and respiration in a sub-Antarctic megaherb from Heard Island". Functional Plant Biology. 42 (6): 553. doi:10.1071/FP14134. ISSN 1445-4416. PMID 32480700.
  25. ^ Stowe, C. J.; Kissling, W. D.; Ohlemüller, R.; Wilson, J. B. (2003-12-01). "Are ecotone properties scale-dependent? A test from a Nothofagustreeline in southern New Zealand". Community Ecology. 4 (1): 36. doi:10.1556/ComEc.4.2003.1.4. ISSN 1588-2756.
  26. ^ Mark, Dickinson & Hofstede 2000, p. 245.
  27. ^ Smale, Mark C.; Wiser, Susan K.; Bergin, Michael J.; Fitzgerald, Neil B. (2018-01-02). "A classification of the geothermal vegetation of the Taupō Volcanic Zone, New Zealand". Journal of the Royal Society of New Zealand. 48 (1): 29. Bibcode:2018JRSNZ..48...21S. doi:10.1080/03036758.2017.1322619. ISSN 0303-6758. S2CID 133647200.
  28. ^ McGlone, M.S. (February 2002). "The Late Quaternary peat, vegetation and climate history of the Southern Oceanic Islands of New Zealand". Quaternary Science Reviews. 21 (4–6): 686. Bibcode:2002QSRv...21..683M. doi:10.1016/S0277-3791(01)00044-0. ISSN 0277-3791.
  29. ^ a b c Mitchell, Anthony D.; Meurk, Colin D.; Wagstaff, Steven J. (1999-06-01). "Evolution of Stilbocarpa, a megaherb from New Zealand's sub-antarctic islands". New Zealand Journal of Botany. 37 (2): 209. doi:10.1080/0028825X.1999.9512628. ISSN 0028-825X.
  30. ^ a b Wagstaff et al. 2007, p. 7.
  31. ^ a b c Komai & Emura 1955, p. 91.
  32. ^ Nagaoka, Nobuyuki; Naoe, Shoji; Takano-Masuya, Yu; Sakai, Shoko (2020-10-14). "Green greenhouse: leaf enclosure for fruit development of an androdioecious vine, Schizopepon bryoniifolius". Proceedings of the Royal Society B: Biological Sciences. 287 (1936): 6. doi:10.1098/rspb.2020.1718. PMC 7657851. PMID 33023418.
  33. ^ a b Elliott et al. 2020, p. 157.
  34. ^ Elliott et al. 2020, p. 166.
  35. ^ Rexer-Huber, Kalinka; Thompson, David; Parker, Graham; Parker, Graham (2020). "White-chinned petrel (Procellaria aequinoctialis) burrow density, occupancy, and population size at the Auckland Islands". Notornis. 67 (1): 397.
  36. ^ Elliott et al. 2020, pp. 163–164.
  37. ^ Komai & Emura 1955, p. 90.
  38. ^ Little et al. 2016, p. 9.
  39. ^ Little et al. 2016, p. 2.
  40. ^ Lord et al. 2013, p. 178.
  41. ^ Buxton, Max N.; Anderson, Barbara J.; Hoare, Robert J. B.; Lord, Janice M. (2019-12-12). "Are moths the missing pollinators in Subantarctic New Zealand?". Polar Research. 38. doi:10.33265/polar.v38.3545. ISSN 1751-8369.
  42. ^ Chilvers, B. Louise (1 October 2021). "Oiled wildlife response planning for subantarctic islands: A review for New Zealand subantarctics". Marine Pollution Bulletin. 171: 5. Bibcode:2021MarPB.17112722C. doi:10.1016/j.marpolbul.2021.112722. ISSN 0025-326X. PMID 34274853.
  43. ^ "Zero Pigs". Department of Conservation (New Zealand). New Zealand Government. Retrieved 22 June 2021.
  44. ^ a b Tasmanian Government 2021, p. 2.
  45. ^ Shiels, Aaron B.; Pitt, William C.; Sugihara, Robert T.; Witmer, Gary W. (April 2014). "Biology and Impacts of Pacific Island Invasive Species. 11. Rattus rattus, the Black Rat (Rodentia: Muridae)". Pacific Science. 68 (2): 155. doi:10.2984/68.2.1. ISSN 0030-8870. S2CID 85862791.
  46. ^ Marchant, R.; Kefford, B. J.; Wasley, J.; King, C. K.; Doube, J.; Nugegoda, D. (2011-04-28). "Response of stream invertebrate communities to vegetation damage from overgrazing by exotic rabbits on subantarctic Macquarie Island". Marine and Freshwater Research. 62 (4): 405. doi:10.1071/MF10317. ISSN 1448-6059 – via CiteSeer.
  47. ^ Tasmanian Government 2021, p. 1.
  48. ^ MEURK, FOGGO & WILSON 1994, p. 148.
  49. ^ Saldivia et al. 2022, p. 615.
  50. ^ Fleming, Theodore H.; Kress, W. John (2013-10-03). Appendix 2. Overview of the Major Families of Plants containing Species That Are Pollinated or Dispersed by Birds or Mammals. University of Chicago Press. p. 498. doi:10.7208/9780226023328-013 (inactive 31 January 2024). ISBN 9780226023328.{{cite book}}: CS1 maint: DOI inactive as of January 2024 (link)
  51. ^ Fleming, Theodore H.; Geiselman, Cullen; Kress, W. John (November 2009). "The evolution of bat pollination: a phylogenetic perspective". Annals of Botany. 104 (6): 1025. doi:10.1093/aob/mcp197. PMC 2766192. PMID 19789175.

Sources edit

External links edit