Form classification is the classification of organisms based on their morphology, which does not necessarily reflect their biological relationships. Form classification, generally restricted to palaeontology, reflects uncertainty; the goal of science is to move "form taxa" to biological taxa whose affinity is known.
Form taxonomy is restricted to fossils that preserve too few characters for a conclusive taxonomic definition or assessment of their biological affinity, but whose study is made easier if a binomial name is available by which to identify them. The term "form classification" is preferred to "form taxonomy"; taxonomy suggests that the classification implies a biological affinity, whereas form classification is about giving a name to a group of morphologically-similar organisms that may not be related.
Forms as taxa
Form taxa are groupings that are based on common overall forms. Early attempts at classification of labyrinthodonts was based on skull shape (the heavily armoured skulls often being the only preserved part). The amount of convergent evolution in the many groups lead to a number of polyphyletic taxa. Such groups are united by a common mode of life, often one that is generalist, in consequence acquiring generally similar body shapes by convergent evolution. Ediacaran biota — whether they are the precursors of the Cambrian explosion of the fossil record, or are unrelated to any modern phylum — can currently only be grouped in "form taxa". Other examples include the seabirds and the "Graculavidae". The latter were initially described as the earliest family of Neornithes but are nowadays recognized to unite a number of unrelated early neornithine lineages, several of which probably later gave rise to the "seabird" form taxon of today.
A "parataxon" (not to be confused with parataxonomy), or "sciotaxon" (Gr. "shadow taxon"), is a classification based on incomplete data: for instance, the larval stage of an organism that cannot be matched up with an adult. It reflects a paucity of data that makes biological classification impossible. A sciotaxon is defined as a taxon thought to be equivalent to a true taxon (orthotaxon), but whose identity cannot be established because the two candidate taxa are preserved in different ways and thus cannot be compared directly.
Form genera and organ genera in botany
In paleobotany, two terms were formerly used in the codes of nomenclature, "form genera" and "organ genera", to mean groups of fossils of a particular part of a plant, such as a leaf or seed, whose parent plant is not known because the fossils were preserved unattached to the parent plant. A later term "morphotaxa" also allows for differences in preservational state. These three terms have been replaced as of 2011 by provisions for "fossil-taxa" that are more similar to the provisions for other types of plants.
Names given to organ genera could only be applied to the organs in question, and could not be extended to the entire organism. Fossil-taxon names can cover several parts of an organism, or several preservational states, but do not compete for priority with any names for the same organism that are based on a non-fossil type.
- wood fossils may have generic names ending in -xylon
- leaf fossils generic names ending in -phyllum
- fruit fossils generic names ending in -carpon, -carpum or -carpus
- pollen fossils generic names ending in -pollis or -pollenoides.
"Form taxon" can more casually be used to describe a wastebasket taxon: either a taxon that is not a natural (monophyletic) group but united by shared plesiomorphies, or a presumably artificial group of organisms whose true relationships are not known, being obscured by ecomorphological similarity. Well-known form taxa of this kind include "ducks", "fish", "reptiles" and "worms".
- Bengtson, S. (1985). "Taxonomy of Disarticulated Fossils". Journal of Paleontology. 59 (6): 1350–1358. JSTOR 1304949.
- Faegri, K. (January 1963). "Organ and Form Genera: Significance and Nomenclatural Treatment". Taxon. 12 (1): 20–28. doi:10.2307/1216676. JSTOR 1216676.
- Watson, D. M. S. (1920): The Structure, Evolution and Origin of the Amphibia. The "Orders' Rachitomi and Stereospondyli. Philosophical Transactions of the Royal Society of London, (series B), Vol. 209, pp. 1–73 Article from JSTOR
- Gee, C. T.; Sander, P. M.; Petzelberger, B. E. M. (2003). "A Miocene rodent nut cache in coastal dunes of the Lower Rhine Embayment, Germany". Palaeontology. 46: 1133. doi:10.1046/j.0031-0239.2003.00337.x.
- McNeill, J.; Barrie, F.R.; Burdet, H.M.; Demoulin, V.; Hawksworth, D.L.; Marhold, K.; Nicolson, D.H.; Prado, J.; Silva, P.C.; Skog, J.E.; Wiersema, J.; Turland, N.J., eds. (2006), International Code of Botanical Nomenclature (Vienna Code). Adopted by the Seventeenth International Botanical Congress Vienna, Austria, July 2005, Rugell, Liechtenstein: A. R. G. Gantner, ISBN 3-906166-48-1 Article 1.2
- Turland, N. (2013), The Code Decoded: A user's guide to the International Code of Nomenclature for algae, fungi, and plants, Regnum Vegetabile Volume 155, Koeltz Scientific Books, ISBN 978-3-87429-433-1
- McNeill, J.; Barrie, F.R.; Buck, W.R.; Demoulin, V.; Greuter, W.; Hawksworth, D.L.; Herendeen, P.S.; Knapp, S.; Marhold, K.; Prado, J.; Prud'homme Van Reine, W.F.; Smith, G.F.; Wiersema, J.H.; Turland, N.J. (2012), International Code of Nomenclature for algae, fungi, and plants (Melbourne Code) adopted by the Eighteenth International Botanical Congress Melbourne, Australia, July 2011, Regnum Vegetabile 154, A.R.G. Gantner Verlag KG, ISBN 978-3-87429-425-6 Article 1.2