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Plants & Fungi
Vascular plants
EOL Text
Collection Sites: world map showing specimen collection locations for Pteridophyta
Tracheobionta (vascular plants) is prey of:
herbivorous vertebrate harvesters
Testudines
Actinopterygii
Anseriformes
Muridae
Odocoileus
Sylvilagus palustris
Based on studies in:
USA: Texas (Lake or pond)
USA: Florida, South Florida (Swamp)
This list may not be complete but is based on published studies.
- L. D. Harris and G. B. Bowman, Vertebrate predator subsystem. In: Grasslands, Systems Analysis and Man, A. I. Breymeyer and G. M. Van Dyne, Eds. (International Biological Programme Series, no. 19, Cambridge Univ. Press, Cambridge, England, 1980), pp. 591-
- B. C. Patten and 40 co-authors, Total ecosystem model for a cove in Lake Texoma. In: Systems Analysis and Simulation in Ecology, B. C. Patten, Ed. (Academic Press, New York, 1975), 3:205-421, from pp. 236, 258, 268.
License | http://creativecommons.org/licenses/by/3.0/ |
Rights holder/Author | Cynthia Sims Parr, Joel Sachs, SPIRE |
Source | http://spire.umbc.edu/fwc/ |
Pteridophytes are the division of plants that include the ferns and so-called fern allies. This is an extremely diverse group of approximately 12,000 species of plants, so divergent that in some classifications, they have been placed in four divisions (e.g., Cronquist et al. 1966). However, three common features unite the group:
1) They are not flowering plants, but instead produce and are dispersed by spores, rather than seeds;
2) They feature a complicated life cycle that includes an alternative of generations, with germination of spores into a gametophyte generation, which is haploid (containing half the normal chromosome number, n) and usually short-lived and inconspicuous and cannot themselves produce spores, but are essential to the reproductive cycle and that exists in a separate stage from the spore-producing plants, sporophytes, which are usually perennial and conspicuous, and have roots, stems (often rhizomatous), and leaves, and are diploid, with 2n chromosomes.
3) They require free (standing) water in order to reproduce, because their flagellate sperm swim to fertilize the eggs; for this reason, many of the species live in moist habitats.
In addition to sexual reproduction through the alternation of generations, many pteridophytes reproduce extensively through vegetative (clonal) propagation, typically from rhizomatous stems, but also from leaves and roots. Because of this, sterile hybrid forms that arise may persist and become common in local regions.
In all but a couple of genera, modern pteridophytes lack secondary growth, including cambium tissue (which produces cork cells and bark on trees). Their characteristics remain similar those found in many of the earliest land plants. However, in contrast to mosses (Bryophyta), they are vascular plants, containing vessels (xylem and phloem) to transport water and nutrients through the stem tissues.
Although no single fern species is of widespread economic importance, over 700 species from 124 genera are grown as ornamentals, either indoors or outdoors for landscaping, and some species are increasingly used in North Amerian gardens where browsing by white-tailed deer (Odocoileus virginiana) is a problem. (Ferns in general are less likely to be browsed by deer than grasses and flowering species, but cultivars of fern species including Athyrium, Dryopteris, and Osmunda are particularly promoted as deer resistant.) Ferns are also sometimes used as a food plant--the emerging stems of some species are gathered in the wild and eaten as a vegetable (fiddlehead ferns, actually the unfurling leaves of various fern species, including Pteridium aquilinum (bracken fern), Matteuccia struthiopteris (ostrich fern), Osmunda cinnamomea (cinnamon fern or buckhorn fern), Osmunda regalis (royal fern), and Athyrium esculentum (vegetable fern), although some of these species are reported to contain potential carcinogens. Many fern species also have traditional medicinal uses.
(Cronquist et al. 1966, Hoshizaki and Moran 2001, Moran 2004, Wagner and Smith 1993, Wikipedia 2012.)
- Cronquist, A., A.L. Takhatajan, and W. Zimmermann. 1966. On the higher taxa of Embryonbionta. Taxon 15: 129–134.
- Hoshizaki, B.J., and R.C. Moran. 2001. Fern Grower's Manual Revised and Expanded Edition. Timber Press. ISBN-13: 9780881924954. 624 p.
- Moran, R.C. 2004. A Natural History of Ferns. Timber Press. ISBN-13: 978-0881926675. 302 p.
- Wagner, W.H., Jr., and A.R. Smith. 1993. Pteridophytes. Ch. 12 in Flora of North America Editorial Committee, eds. Flora of North America north of Mexico 1: 247–266. New York: Oxford University Press.
- Wikipedia. 2012. Fiddlehead fern [Internet]. Wikipedia, The Free Encyclopedia. 2012 Jun 17, 07:03 UTC [cited 2012 Jun 27]. Available from: http://en.wikipedia.org/w/index.php?title=Fiddlehead_fern&oldid=497981791.
License | http://creativecommons.org/licenses/by-nc-sa/3.0/ |
Rights holder/Author | Jacqueline Courteau, Jacqueline Courteau |
Source | No source database. |
Pteridophytes are the division of plants that include the ferns and so-called fern allies. This is an extremely diverse group of approximately 12,000 species of plants, so divergent that in some classifications, they have been placed in four divisions (e.g., Cronquist et al. 1966). However, three common features unite the group:
1) They are not flowering plants, but instead produce and are dispersed by spores, rather than seeds;
2) They feature a complicated life cycle that includes an alternative of generations, with germination of spores into a gametophyte generation, which is haploid (containing half the normal chromosome number, n) and usually short-lived and inconspicuous and cannot themselves produce spores, but are essential to the reproductive cycle and that exists in a separate stage from the spore-producing plants, sporophytes, which are usually perennial and conspicuous, and have roots, stems (often rhizomatous), and leaves, and are diploid, with 2n chromosomes.
3) They require free (standing) water in order to reproduce, because their flagellate sperm swim to fertilize the eggs; for this reason, many of the species live in moist habitats.
In addition to sexual reproduction through the alternation of generations, many pteridophytes reproduce extensively through vegetative (clonal) propagation, typically from rhizomatous stems, but also from leaves and roots. Because of this, sterile hybrid forms that arise may persist and become common in local regions.
In all but a couple of genera, modern pteridophytes lack secondary growth, including cambium tissue (which produces cork cells and bark on trees). Their characteristics remain similar those found in many of the earliest land plants. However, in contrast to mosses (Bryophyta), they are vascular plants, containing vessels (xylem and phloem) to transport water and nutrients through the stem tissues.
Although no single fern species is of widespread economic importance, over 700 species from 124 genera are grown as ornamentals, either indoors or outdoors for landscaping, and some species are increasingly used in North Amerian gardens where browsing by white-tailed deer (Odocoileus virginiana) is a problem. (Ferns in general are less likely to be browsed by deer than grasses and flowering species, but cultivars of fern species including Athyrium, Dryopteris, and Osmunda are particularly promoted as deer resistant.) Ferns are also sometimes used as a food plant--the emerging stems of some species are gathered in the wild and eaten as a vegetable (fiddlehead ferns, actually the unfurling leaves of various fern species, including Pteridium aquilinum (bracken fern), Matteuccia struthiopteris (ostrich fern), Osmunda cinnamomea (cinnamon fern or buckhorn fern), Osmunda regalis (royal fern), and Athyrium esculentum (vegetable fern), although some of these species are reported to contain potential carcinogens. Many fern species also have traditional medicinal uses.
(Cronquist et al. 1966, Hoshizaki and Moran 2001, Moran 2004, Wagner and Smith 1993, Wikipedia 2012.)
- Cronquist, A., A.L. Takhatajan, and W. Zimmermann. 1966. On the higher taxa of Embryonbionta. Taxon 15: 129–134.
- Hoshizaki, B.J., and R.C. Moran. 2001. Fern Grower's Manual Revised and Expanded Edition. Timber Press. ISBN-13: 9780881924954. 624 p.
- Moran, R.C. 2004. A Natural History of Ferns. Timber Press. ISBN-13: 978-0881926675. 302 p.
- Wagner, W.H., Jr., and A.R. Smith. 1993. Pteridophytes. Ch. 12 in Flora of North America Editorial Committee, eds. Flora of North America north of Mexico 1: 247–266. New York: Oxford University Press.
- Wikipedia. 2012. Fiddlehead fern [Internet]. Wikipedia, The Free Encyclopedia. 2012 Jun 17, 07:03 UTC [cited 2012 Jun 27]. Available from: http://en.wikipedia.org/w/index.php?title=Fiddlehead_fern&oldid=497981791.
License | http://creativecommons.org/licenses/by-nc-sa/3.0/ |
Rights holder/Author | Jacqueline Courteau, Jacqueline Courteau |
Source | No source database. |
Ferns of Arizona - Arizona, USA
Ontario Ferns - Ontario, Canada
Identifying Australian Rainforest Plants,Trees and Fungi: Ferns - Australia
License | http://creativecommons.org/licenses/by/3.0/ |
Rights holder/Author | Tracy Barbaro, Tracy Barbaro |
Source | http://eol.org/collections/108 |
Ferns of Arizona - Arizona, USA
Ontario Ferns - Ontario, Canada
Identifying Australian Rainforest Plants,Trees and Fungi: Ferns - Australia
License | http://creativecommons.org/licenses/by/3.0/ |
Rights holder/Author | Tracy Barbaro, Tracy Barbaro |
Source | http://eol.org/collections/108 |
Surface tension flings spores: fern
The spores of one fern are launched from the sporangium using a mechanism based on surface tension and evaporation.
"A mechanism based on the surface tension of water is used by a fern that forcibly discharges its spores from the sporangium--evaporation decreases the volume of water and increases the surface curvature in a series of cuplike dead cells until the sustainable cohesion is exceeded; water then vaporizes and tension is relieved by a movement analogous to that involved in throwing a spear (Steward 1968)." (Vogel 2003:449)
Watch video
Learn more about this functional adaptation.
- Steven Vogel. 2003. Comparative Biomechanics: Life's Physical World. Princeton: Princeton University Press. 580 p.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/8cf926d2aecea12f976a26bf1f3bd192 |
Surface tension flings spores: fern
The spores of one fern are launched from the sporangium using a mechanism based on surface tension and evaporation.
"A mechanism based on the surface tension of water is used by a fern that forcibly discharges its spores from the sporangium--evaporation decreases the volume of water and increases the surface curvature in a series of cuplike dead cells until the sustainable cohesion is exceeded; water then vaporizes and tension is relieved by a movement analogous to that involved in throwing a spear (Steward 1968)." (Vogel 2003:449)
Watch video
Learn more about this functional adaptation.
- Steven Vogel. 2003. Comparative Biomechanics: Life's Physical World. Princeton: Princeton University Press. 580 p.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/8cf926d2aecea12f976a26bf1f3bd192 |
Signal directs sperm: fern
The sperm of ferns detect unfertilized archegonia via a malate signal.
"In higher plants, we find positive chemotaxis in fern sperms, which respond to a malate signal from unfertilized archegonia." (Bar-Cohen 2006:474)
Learn more about this functional adaptation.
- Yoseph Bar-Cohen. 2006. Biomimetics: biologically inspired technologies. Boca Raton, FL: CRC/Taylor & Francis. 527 p.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/87bdb081a40f5c0a9921c934881dd4f5 |
Signal directs sperm: fern
The sperm of ferns detect unfertilized archegonia via a malate signal.
"In higher plants, we find positive chemotaxis in fern sperms, which respond to a malate signal from unfertilized archegonia." (Bar-Cohen 2006:474)
Learn more about this functional adaptation.
- Yoseph Bar-Cohen. 2006. Biomimetics: biologically inspired technologies. Boca Raton, FL: CRC/Taylor & Francis. 527 p.
License | http://creativecommons.org/licenses/by-nc/3.0/ |
Rights holder/Author | (c) 2008-2009 The Biomimicry Institute |
Source | http://www.asknature.org/strategy/87bdb081a40f5c0a9921c934881dd4f5 |