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Wednesday, September 9, 2020

Taxonomy (biology)

From Wikipedia, the free encyclopedia
 
In biology, taxonomy (from Ancient Greek τάξις (taxis), meaning 'arrangement', and -νομία (-nomia), meaning 'method') is the science of naming, defining (circumscribing) and classifying groups of biological organisms on the basis of shared characteristics. Organisms are grouped together into taxa (singular: taxon) and these groups are given a taxonomic rank; groups of a given rank can be aggregated to form a super-group of higher rank, thus creating a taxonomic hierarchy. The principal ranks in modern use are domain, kingdom, phylum (division is sometimes used in botany in place of phylum), class, order, family, genus, and species. The Swedish botanist Carl Linnaeus is regarded as the founder of the current system of taxonomy, as he developed a system known as Linnaean taxonomy for categorizing organisms and binomial nomenclature for naming organisms.

With the advent of such fields of study as phylogenetics, cladistics, and systematics, the Linnaean system has progressed to a system of modern biological classification based on the evolutionary relationships between organisms, both living and extinct.

Definition

The exact definition of taxonomy varies from source to source, but the core of the discipline remains: the conception, naming, and classification of groups of organisms. As points of reference, recent definitions of taxonomy are presented below:
  1. Theory and practice of grouping individuals into species, arranging species into larger groups, and giving those groups names, thus producing a classification.
  2. A field of science (and major component of systematics) that encompasses description, identification, nomenclature, and classification
  3. The science of classification, in biology the arrangement of organisms into a classification
  4. "The science of classification as applied to living organisms, including study of means of formation of species, etc."
  5. "The analysis of an organism's characteristics for the purpose of classification"
  6. "Systematics studies phylogeny to provide a pattern that can be translated into the classification and names of the more inclusive field of taxonomy" (listed as a desirable but unusual definition)
The varied definitions either place taxonomy as a sub-area of systematics (definition 2), invert that relationship (definition 6), or appear to consider the two terms synonymous. There is some disagreement as to whether biological nomenclature is considered a part of taxonomy (definitions 1 and 2), or a part of systematics outside taxonomy. For example, definition 6 is paired with the following definition of systematics that places nomenclature outside taxonomy:
  • Systematics: "The study of the identification, taxonomy, and nomenclature of organisms, including the classification of living things with regard to their natural relationships and the study of variation and the evolution of taxa".
A whole set of terms including taxonomy, systematic biology, systematics, biosystematics, scientific classification, biological classification, and phylogenetics have at times had overlapping meanings – sometimes the same, sometimes slightly different, but always related and intersecting. The broadest meaning of "taxonomy" is used here. The term itself was introduced in 1813 by de Candolle, in his Théorie élémentaire de la botanique.

Monograph and taxonomic revision

A taxonomic revision or taxonomic review is a novel analysis of the variation patterns in a particular taxon. This analysis may be executed on the basis of any combination of the various available kinds of characters, such as morphological, anatomical, palynological, biochemical and genetic. A monograph or complete revision is a revision that is comprehensive for a taxon for the information given at a particular time, and for the entire world. Other (partial) revisions may be restricted in the sense that they may only use some of the available character sets or have a limited spatial scope. A revision results in a conformation of or new insights in the relationships between the subtaxa within the taxon under study, which may result in a change in the classification of these subtaxa, the identification of new subtaxa, or the merger of previous subtaxa.

Alpha and beta taxonomy

The term "alpha taxonomy" is primarily used today to refer to the discipline of finding, describing, and naming taxa, particularly species. In earlier literature, the term had a different meaning, referring to morphological taxonomy, and the products of research through the end of the 19th century.

William Bertram Turrill introduced the term "alpha taxonomy" in a series of papers published in 1935 and 1937 in which he discussed the philosophy and possible future directions of the discipline of taxonomy.
… there is an increasing desire amongst taxonomists to consider their problems from wider viewpoints, to investigate the possibilities of closer co-operation with their cytological, ecological and genetics colleagues and to acknowledge that some revision or expansion, perhaps of a drastic nature, of their aims and methods, may be desirable … Turrill (1935) has suggested that while accepting the older invaluable taxonomy, based on structure, and conveniently designated "alpha", it is possible to glimpse a far-distant taxonomy built upon as wide a basis of morphological and physiological facts as possible, and one in which "place is found for all observational and experimental data relating, even if indirectly, to the constitution, subdivision, origin, and behaviour of species and other taxonomic groups". Ideals can, it may be said, never be completely realized. They have, however, a great value of acting as permanent stimulants, and if we have some, even vague, ideal of an "omega" taxonomy we may progress a little way down the Greek alphabet. Some of us please ourselves by thinking we are now groping in a "beta" taxonomy.
Turrill thus explicitly excludes from alpha taxonomy various areas of study that he includes within taxonomy as a whole, such as ecology, physiology, genetics, and cytology. He further excludes phylogenetic reconstruction from alpha taxonomy (pp. 365–366). 

Later authors have used the term in a different sense, to mean the delimitation of species (not subspecies or taxa of other ranks), using whatever investigative techniques are available, and including sophisticated computational or laboratory techniques. Thus, Ernst Mayr in 1968 defined "beta taxonomy" as the classification of ranks higher than species.
An understanding of the biological meaning of variation and of the evolutionary origin of groups of related species is even more important for the second stage of taxonomic activity, the sorting of species into groups of relatives ("taxa") and their arrangement in a hierarchy of higher categories. This activity is what the term classification denotes; it is also referred to as "beta taxonomy".

Microtaxonomy and macrotaxonomy

How species should be defined in a particular group of organisms gives rise to practical and theoretical problems that are referred to as the species problem. The scientific work of deciding how to define species has been called microtaxonomy. By extension, macrotaxonomy is the study of groups at the higher taxonomic ranks subgenus and above.

History

While some descriptions of taxonomic history attempt to date taxonomy to ancient civilizations, a truly scientific attempt to classify organisms did not occur until the 18th century. Earlier works were primarily descriptive and focused on plants that were useful in agriculture or medicine. There are a number of stages in this scientific thinking. Early taxonomy was based on arbitrary criteria, the so-called "artificial systems", including Linnaeus's system of sexual classification. Later came systems based on a more complete consideration of the characteristics of taxa, referred to as "natural systems", such as those of de Jussieu (1789), de Candolle (1813) and Bentham and Hooker (1862–1863). These were pre-evolutionary in thinking. The publication of Charles Darwin's On the Origin of Species (1859) led to new ways of thinking about classification based on evolutionary relationships. This was the concept of phyletic systems, from 1883 onwards. This approach was typified by those of Eichler (1883) and Engler (1886–1892). The advent of molecular genetics and statistical methodology allowed the creation of the modern era of "phylogenetic systems" based on cladistics, rather than morphology alone.

Pre-Linnaean

Early taxonomists

Naming and classifying our surroundings has probably been taking place as long as mankind has been able to communicate. It would always have been important to know the names of poisonous and edible plants and animals in order to communicate this information to other members of the family or group. Medicinal plant illustrations show up in Egyptian wall paintings from c. 1500 BC, indicating that the uses of different species were understood and that a basic taxonomy was in place.

Ancient times

Description of rare animals (写生珍禽图), by Song dynasty painter Huang Quan (903–965)
 
Organisms were first classified by Aristotle (Greece, 384–322 BC) during his stay on the Island of Lesbos. He classified beings by their parts, or in modern terms attributes, such as having live birth, having four legs, laying eggs, having blood, or being warm-bodied. He divided all living things into two groups: plants and animals. Some of his groups of animals, such as Anhaima (animals without blood, translated as invertebrates) and Enhaima (animals with blood, roughly the vertebrates), as well as groups like the sharks and cetaceans, are still commonly used today. His student Theophrastus (Greece, 370–285 BC) carried on this tradition, mentioning some 500 plants and their uses in his Historia Plantarum. Again, several plant groups currently still recognized can be traced back to Theophrastus, such as Cornus, Crocus, and Narcissus.

Medieval

Taxonomy in the Middle Ages was largely based on the Aristotelian system, with additions concerning the philosophical and existential order of creatures. This included concepts such as the Great chain of being in the Western scholastic tradition, again deriving ultimately from Aristotle. Aristotelian system did not classify plants or fungi, due to the lack of microscope at the time, as his ideas were based on arranging the complete world in a single continuum, as per the scala naturae (the Natural Ladder). This, as well, was taken into consideration in the Great chain of being. Advances were made by scholars such as Procopius, Timotheos of Gaza, Demetrios Pepagomenos, and Thomas Aquinas. Medieval thinkers used abstract philosophical and logical categorizations more suited to abstract philosophy than to pragmatic taxonomy.

Renaissance and Early Modern

During the Renaissance, the Age of Reason, and the Enlightenment, categorizing organisms became more prevalent, and taxonomic works became ambitious enough to replace the ancient texts. This is sometimes credited to the development of sophisticated optical lenses, which allowed the morphology of organisms to be studied in much greater detail. One of the earliest authors to take advantage of this leap in technology was the Italian physician Andrea Cesalpino (1519–1603), who has been called "the first taxonomist". His magnum opus De Plantis came out in 1583, and described more than 1500 plant species. Two large plant families that he first recognized are still in use today: the Asteraceae and Brassicaceae. Then in the 17th century John Ray (England, 1627–1705) wrote many important taxonomic works. Arguably his greatest accomplishment was Methodus Plantarum Nova (1682), in which he published details of over 18,000 plant species. At the time, his classifications were perhaps the most complex yet produced by any taxonomist, as he based his taxa on many combined characters. The next major taxonomic works were produced by Joseph Pitton de Tournefort (France, 1656–1708). His work from 1700, Institutiones Rei Herbariae, included more than 9000 species in 698 genera, which directly influenced Linnaeus, as it was the text he used as a young student.

The Linnaean era

Title page of Systema Naturae, Leiden, 1735

The Swedish botanist Carl Linnaeus (1707–1778) ushered in a new era of taxonomy. With his major works Systema Naturae 1st Edition in 1735, Species Plantarum in 1753, and Systema Naturae 10th Edition, he revolutionized modern taxonomy. His works implemented a standardized binomial naming system for animal and plant species, which proved to be an elegant solution to a chaotic and disorganized taxonomic literature. He not only introduced the standard of class, order, genus, and species, but also made it possible to identify plants and animals from his book, by using the smaller parts of the flower. Thus the Linnaean system was born, and is still used in essentially the same way today as it was in the 18th century. Currently, plant and animal taxonomists regard Linnaeus' work as the "starting point" for valid names (at 1753 and 1758 respectively). Names published before these dates are referred to as "pre-Linnaean", and not considered valid (with the exception of spiders published in Svenska Spindlar). Even taxonomic names published by Linnaeus himself before these dates are considered pre-Linnaean.

Modern system of classification

Evolution of the vertebrates at class level, width of spindles indicating number of families. Spindle diagrams are typical for evolutionary taxonomy
 
The same relationship, expressed as a cladogram typical for cladistics
 
Whereas Linnaeus aimed simply to create readily identifiable taxa, the idea of the Linnaean taxonomy as translating into a sort of dendrogram of the animal and plant kingdoms was formulated toward the end of the 18th century, well before On the Origin of Species was published. Among early works exploring the idea of a transmutation of species were Erasmus Darwin's 1796 Zoönomia and Jean-Baptiste Lamarck's Philosophie Zoologique of 1809. The idea was popularized in the Anglophone world by the speculative but widely read Vestiges of the Natural History of Creation, published anonymously by Robert Chambers in 1844.

With Darwin's theory, a general acceptance quickly appeared that a classification should reflect the Darwinian principle of common descent. Tree of life representations became popular in scientific works, with known fossil groups incorporated. One of the first modern groups tied to fossil ancestors was birds. Using the then newly discovered fossils of Archaeopteryx and Hesperornis, Thomas Henry Huxley pronounced that they had evolved from dinosaurs, a group formally named by Richard Owen in 1842. The resulting description, that of dinosaurs "giving rise to" or being "the ancestors of" birds, is the essential hallmark of evolutionary taxonomic thinking. As more and more fossil groups were found and recognized in the late 19th and early 20th centuries, palaeontologists worked to understand the history of animals through the ages by linking together known groups. With the modern evolutionary synthesis of the early 1940s, an essentially modern understanding of the evolution of the major groups was in place. As evolutionary taxonomy is based on Linnaean taxonomic ranks, the two terms are largely interchangeable in modern use.

The cladistic method has emerged since the 1960s. In 1958, Julian Huxley used the term clade. Later, in 1960, Cain and Harrison introduced the term cladistic. The salient feature is arranging taxa in a hierarchical evolutionary tree, ignoring ranks. A taxon is called monophyletic, if it includes all the descendants of an ancestral form. Groups that have descendant groups removed from them are termed paraphyletic, while groups representing more than one branch from the tree of life are called polyphyletic. The International Code of Phylogenetic Nomenclature or PhyloCode is intended to regulate the formal naming of clades. Linnaean ranks will be optional under the PhyloCode, which is intended to coexist with the current, rank-based codes.

Kingdoms and domains

The basic scheme of modern classification. Many other levels can be used; domain, the highest level within life, is both new and disputed.
Well before Linnaeus, plants and animals were considered separate Kingdoms. Linnaeus used this as the top rank, dividing the physical world into the plant, animal and mineral kingdoms. As advances in microscopy made classification of microorganisms possible, the number of kingdoms increased, five- and six-kingdom systems being the most common.

Domains are a relatively new grouping. First proposed in 1977, Carl Woese's three-domain system was not generally accepted until later. One main characteristic of the three-domain method is the separation of Archaea and Bacteria, previously grouped into the single kingdom Bacteria (a kingdom also sometimes called Monera), with the Eukaryota for all organisms whose cells contain a nucleus. A small number of scientists include a sixth kingdom, Archaea, but do not accept the domain method.

Thomas Cavalier-Smith, who has published extensively on the classification of protists, has recently proposed that the Neomura, the clade that groups together the Archaea and Eucarya, would have evolved from Bacteria, more precisely from Actinobacteria. His 2004 classification treated the archaeobacteria as part of a subkingdom of the kingdom Bacteria, i.e., he rejected the three-domain system entirely. Stefan Luketa in 2012 proposed a five "dominion" system, adding Prionobiota (acellular and without nucleic acid) and Virusobiota (acellular but with nucleic acid) to the traditional three domains.

Recent comprehensive classifications

Partial classifications exist for many individual groups of organisms and are revised and replaced as new information becomes available; however, comprehensive, published treatments of most or all life are rarer; recent examples are that of Adl et al., 2012 and 2019, which covers eukaryotes only with an emphasis on protists, and Ruggiero et al., 2015, covering both eukaryotes and prokaryotes to the rank of Order, although both exclude fossil representatives. A separate compilation (Ruggiero, 2014) covers extant taxa to the rank of family. Other, database-driven treatments include the Encyclopedia of Life, the Global Biodiversity Information Facility, the NCBI taxonomy database, the Interim Register of Marine and Nonmarine Genera, the Open Tree of Life, and the Catalogue of Life. The Paleobiology Database is a resource for fossils.

Application

Biological taxonomy is a sub-discipline of biology, and is generally practiced by biologists known as "taxonomists", though enthusiastic naturalists are also frequently involved in the publication of new taxa. Because taxonomy aims to describe and organize life, the work conducted by taxonomists is essential for the study of biodiversity and the resulting field of conservation biology.

Classifying organisms

Biological classification is a critical component of the taxonomic process. As a result, it informs the user as to what the relatives of the taxon are hypothesized to be. Biological classification uses taxonomic ranks, including among others (in order from most inclusive to least inclusive): Domain, Kingdom, Phylum, Class, Order, Family, Genus, Species, and Strain.

Taxonomic descriptions

The "definition" of a taxon is encapsulated by its description or its diagnosis or by both combined. There are no set rules governing the definition of taxa, but the naming and publication of new taxa is governed by sets of rules. In zoology, the nomenclature for the more commonly used ranks (superfamily to subspecies), is regulated by the International Code of Zoological Nomenclature (ICZN Code). In the fields of phycology, mycology, and botany, the naming of taxa is governed by the International Code of Nomenclature for algae, fungi, and plants (ICN).
The initial description of a taxon involves five main requirements:
  1. The taxon must be given a name based on the 26 letters of the Latin alphabet (a binomial for new species, or uninomial for other ranks).
  2. The name must be unique (i.e. not a homonym).
  3. The description must be based on at least one name-bearing type specimen.
  4. It should include statements about appropriate attributes either to describe (define) the taxon or to differentiate it from other taxa (the diagnosis, ICZN Code, Article 13.1.1, ICN, Article 38). Both codes deliberately separate defining the content of a taxon (its circumscription) from defining its name.
  5. These first four requirements must be published in a work that is obtainable in numerous identical copies, as a permanent scientific record.
However, often much more information is included, like the geographic range of the taxon, ecological notes, chemistry, behavior, etc. How researchers arrive at their taxa varies: depending on the available data, and resources, methods vary from simple quantitative or qualitative comparisons of striking features, to elaborate computer analyses of large amounts of DNA sequence data.

Author citation

An "authority" may be placed after a scientific name. The authority is the name of the scientist or scientists who first validly published the name. For example, in 1758 Linnaeus gave the Asian elephant the scientific name Elephas maximus, so the name is sometimes written as "Elephas maximus Linnaeus, 1758". The names of authors are frequently abbreviated: the abbreviation L., for Linnaeus, is commonly used. In botany, there is, in fact, a regulated list of standard abbreviations. The system for assigning authorities differs slightly between botany and zoology. However, it is standard that if the genus of a species has been changed since the original description, the original authority's name is placed in parentheses.

Phenetics

In phenetics, also known as taximetrics, or numerical taxonomy, organisms are classified based on overall similarity, regardless of their phylogeny or evolutionary relationships. It results in a measure of evolutionary "distance" between taxa. Phenetic methods have become relatively rare in modern times, largely superseded by cladistic analyses, as phenetic methods do not distinguish common ancestral (or plesiomorphic) traits from new common (or apomorphic) traits. However, certain phenetic methods, such as neighbor joining, have found their way into cladistics, as a reasonable approximation of phylogeny when more advanced methods (such as Bayesian inference) are too computationally expensive.

Databases

Modern taxonomy uses database technologies to search and catalogue classifications and their documentation. While there is no commonly used database, there are comprehensive databases such as the Catalogue of Life, which attempts to list every documented species. The catalogue listed 1.64 million species for all kingdoms as of April 2016, claiming coverage of more than three quarters of the estimated species known to modern science.

List of the largest genera of flowering plants

Agamospecies in the Ranunculus auricomus complex help to swell the number of species in the genus Ranunculus.
 
There are 57 genera of flowering plants estimated to contain at least 500 described species.[DJS--per genus?] The largest of these is currently the legume genus Astragalus (milk-vetches), with over 3,000 species.

The sizes of plant genera vary widely from those containing a single species to genera containing thousands of species, and this disparity became clear early in the history of plant classification. The largest genus in Carl Linnaeus' seminal Species Plantarum was Euphorbia, with 56 species; Linnaeus believed that no genus should contain more than 100 species.

Part of the disparity in genus sizes is attributable to historical factors. According to a hypothesis published by Max Walters in 1961, the size of plant genera is related to the age, not of the taxon itself, but of the concept of the taxon in the minds of taxonomists. Plants which grew in Europe, where most of the early taxonomy was based, were therefore divided into relatively small genera, while those from the tropics were grouped into much larger and more heterogeneous genera. Likewise, plants which shared common medicinal properties, such as the many species of Euphorbia, were united into a single genus, while plants of diverse uses, such as the grasses, were split into many genera. Where there were many classical names for groups of plants, such as in Apiaceae / Umbelliferae or Brassicaceae / Cruciferae, small genera were defined, whereas groups not subdivided by classical authors remained as larger genera, such as Carex. A number of biological factors also influence the number of species. For instance, the occurrence of apomixis allows the recognition of large numbers of agamospecies, and such taxa have helped to bolster genera such as Ranunculus and Potentilla.

The introduction of infrageneric taxa (such as the subgenus, section and series) in the 19th century by botanists including Augustin Pyrame de Candolle allowed the retention of large genera that would otherwise have become unwieldy. E. J. H. Corner believed that studying large genera might enable greater insights into evolutionary biology, and he concentrated his efforts on large tropical genera such as Ficus.

Largest genera

A total of 57 genera of flowering plants contain at least 500 species, according to a 2004 analysis by the botanical taxonomist David Frodin. The actual numbers of species are imprecisely known, as many of the genera have not been the subject of recent monographs. For instance, estimates of the number of species in the orchid genus Pleurothallis range from 1,120 to 2,500. Genera from other groups of vascular plants, but which have similarly large numbers of species, include Selaginella, Asplenium and Cyathea.

A legume with inflorescences of up to 40 elongated, ivory-coloured flowers, and pinnate leaves with many pairs of leaflets.
Astragalus is the largest flowering plant genus, with more than 3,200 species, including Astragalus agnicidus.
 
Five orchid flowers, each with spotted tepals and a pink labellum.
Bulbophyllum is the second largest flowering plant genus, with more than 2,000 species, including Bulbophyllum guttulatum.
 
A shrub with large, leathery, simple leaves, and bearing clusters of round, green fruit.
Psychotria is the third largest flowering plant genus, with more than 1,900 species, including Psychotria mariniana.
 
A group of unbranched herbs grow beside a plant label. The upper leaves and bracts grade from green to yellow.
Euphorbia is the fourth largest flowering plant genus, with more than 1,800 species, including Euphorbia amygdaloides.
 
Several small, grass-like plants with thin leaves, each with a stalk bearing a cluster of small round fruits.
Carex is the fifth largest flowering plant genus, with more than 1,700 species, including Carex pilulifera.
 
Genera of flowering plants with at least 500 species
Rank Genus Species Family Species list
1 Astragalus 3,270 Fabaceae List of Astragalus species
2 Bulbophyllum 2,032 Orchidaceae List of Bulbophyllum species
3 Psychotria 1,951 Rubiaceae List of Psychotria species
4 Euphorbia 1,836 Euphorbiaceae List of Euphorbia species
5 Carex 1,795 Cyperaceae List of Carex species
6 Begonia 1,484 Begoniaceae List of Begonia species
7 Dendrobium 1,371 Orchidaceae List of Dendrobium species
8 Acacia c. 1,353 Fabaceae List of Acacia species
9 Solanum c. 1,250 Solanaceae List of Solanum species
10 Senecio c. 1,250 Asteraceae List of Senecio species
11 Croton 1,223 Euphorbiaceae List of Croton species
12 Pleurothallis 1,120+ Orchidaceae List of Pleurothallis species
13 Eugenia 1,113 Myrtaceae List of Eugenia species
14 Piper 1,055 Piperaceae List of Piper species
15 Ardisia 1,046 Primulaceae List of Ardisia species
16 Syzygium 1,041 Myrtaceae List of Syzygium species
17 Rhododendron c. 1,000 Ericaceae List of Rhododendron species
18 Miconia 1,000 Melastomataceae List of Miconia species
19 Peperomia 1,000 Piperaceae List of Peperomia species
20 Salvia 945 Lamiaceae List of Salvia species
21 Erica 860 Ericaceae List of Erica species
22 Impatiens 850 Balsaminaceae List of Impatiens species
23 Cyperus 839 Cyperaceae List of Cyperus species
24 Phyllanthus 833 Phyllanthaceae List of Phyllanthus species
25 Allium 815 Amaryllidaceae List of Allium species
26 Epidendrum 800 Orchidaceae List of Epidendrum species
27 Vernonia 800–1,000 Asteraceae List of Vernonia species
28 Lepanthes c. 800 Orchidaceae List of Lepanthes species
29 Anthurium 789 Araceae List of Anthurium species
30 Diospyros 767 Ebenaceae List of Diospyros species
31 Ficus 750 Moraceae
32 Indigofera 700+ Fabaceae
33 Justicia c. 700[4] Acanthaceae List of Justicia species
34 Silene 700 Caryophyllaceae
35 Oxalis 700 Oxalidaceae
36 Crotalaria 699 Fabaceae
37 Centaurea 695 Asteraceae
38 Cassia 692 Fabaceae
39 Eucalyptus 681 Myrtaceae List of Eucalyptus species
40 Oncidium 680 Orchidaceae
41 Galium 661 Rubiaceae List of Galium species
42 Cousinia 655 Asteraceae
43 Ipomoea 650 Convolvulaceae
44 Dioscorea 631 Dioscoreaceae
45 Cyrtandra 622 Gesneriaceae
46 Helichrysum 600 Asteraceae
47 Ranunculus 600 Ranunculaceae List of Ranunculus species
48 Habenaria 600 Orchidaceae List of Habenaria species
49 Schefflera 584 Araliaceae List of Schefflera species
50 Ixora 561 Rubiaceae List of Ixora species
51 Berberis 556 Berberidaceae List of Berberis species
52 Quercus 531 Fagaceae List of Quercus species
53 Pandanus c. 520 Pandanaceae List of Pandanus species
54 Panicum 500+ Poaceae List of Panicum species
55 Eria 500 Orchidaceae
56 Polygala 500 Polygalaceae
57 Potentilla 500 Rosaceae List of Potentilla species

Argiope (spider)

From Wikipedia, the free encyclopedia
 
Argiope
Temporal range: Neogene–present
Reflective silver argiope in a stabilimentum-free web in California.jpg
Reflective silver argiope in a web (without stabilimentum) in California
Scientific classification e
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Chelicerata
Class: Arachnida
Order: Araneae
Infraorder: Araneomorphae
Family: Araneidae
Genus: Argiope
Audouin, 1826
Type species
Aranea lobata
Pallas, 1772
Species
See text.
Synonyms
  • Austrargiope
  • Brachygea
  • Chaetargiope
  • Coganargiope
  • Heterargiope

The genus Argiope includes rather large spiders that often have a strikingly coloured abdomen. These spiders are distributed throughout the world. Most countries in tropical or temperate climates host one or more species that are similar in appearance. The etymology of Argiope is from a Latin word argentum meaning silver. The carapace of Argiope species is typically covered in silvery hairs.

Common names

Argiope sp. blending in to elaborate stabilimentum in Tanzania
 
An argiope's web with stabilimentum in Independence, Missouri
 
Argiope bruennichi is commonly known as the wasp spider. In Australia, Argiope keyserlingi and Argiope aetherea are known as St Andrew's cross spiders, for their habit of resting in the web with paired legs outstretched in the shape of an X and mirroring the large white web decoration (the cross of St. Andrew having the same form). This white zigzag in the centre of its web is called the stabilimentum or web decoration.

In North America, Argiope aurantia is commonly known as the black and yellow garden spider, zipper spider, corn spider, or writing spider, because of the similarity of the web stabilimenta to writing. 

The East Asian species Argiope amoena is known in Japan as kogane-gumo. In the Philippines, they are known as gagambang ekis ("X spider"), and gagambang pari ("priest spider", due to the spider's body resembling a priest's head with a mitre).

Web

The average orb web is practically invisible, and it is easy to blunder into one and end up covered with a sticky web. The visible pattern of banded silk made by Argiope is pure white, and some species make an "X" form, or a zigzag type of web (often with a hollow centre). The spider then aligns one pair of its legs with each of the four lines in the hollow "X", making a complete "X" of white lines with a very eye-catching spider forming its centre.

The zigzag patterns, called stabilimenta, reflect UV light. They have been shown to play a role in attracting prey to the web, and possibly in preventing its destruction by large animals. The centres of their large webs are often just under 1 metre above the ground, so they are too low for anything much larger than a rabbit to walk under. The overtness of the spider and its web thus has been speculated to prevent larger creatures from accidentally destroying the web and possibly crushing the spider underfoot.

Other studies suggest that the stabilimenta may actually lead predators to the spider; species such as A. keyserlingi place their web predominantly in closed, complex habitats such as among sedges.

As Argiope sit in the centre of their web during the day, they have developed several responses to predators, such as dropping off the web, retreating to the periphery of the web, or even rapidly pumping the web in bursts of up to 30 seconds, similar to the motion done by the unrelated Pholcus phalangioides.

Reproduction

The male spider is much smaller than the female, and unassumingly marked. When it is time to mate, the male spins a companion web alongside the female's. After mating, the female lays her eggs, placing her egg sac into the web. The sac contains between 400 and 1400 eggs.

These eggs hatch in autumn, but the spiderlings overwinter in the sac and emerge during the spring. The egg sac is composed of multiple layers of silk and protects its contents from damage; however, many species of insects have been observed to parasitise the egg sacs.

Bite

Like almost all other spiders, Argiope are harmless to humans. As is the case with most garden spiders, they eat insects, and they are capable of consuming prey up to twice their size. A. savigny was even reported to occasionally feed on the small bat Rhynchonycteris naso.

They can potentially bite if grabbed, but other than for defense, they do not attack large animals. Their venom is not regarded as a serious medical problem for humans; it often contains a wide variety of polyamine toxins with potential as therapeutic medicinal agents. Notable among these is the argiotoxin ArgTX-636 (A. lobata).


A bite by the black and yellow garden spider (Argiope aurantia) is comparable to a bee sting, with redness and swelling. For a healthy adult, a bite is not considered an issue.


Though they are not aggressive spiders, the very young, elderly, those with compromised immune systems, or those with known venom allergies should exercise caution, just as one would around a beehive.

Taxonomy

The first description of the genus Argiope is attributed to Jean Victoire Audouin in 1826, although he wrote that the genus was established by Savigny. In the first edition of the work in which the description appeared (Description de l'Égypte: Histoire Naturelle), Audouin used the spelling "Argyope", for both the French vernacular name and the Latin generic name. In the second edition, he continued to use "Argyope" for the French vernacular name, but the first mention of the Latin generic name had the spelling "Argiope", although the binomial names of the species continued to use "Argyope". This led to controversy as to whether Audouin had intended to correct the spelling of the generic name, which is derived from the Greek αργιόπη. In 1975, the International Commission on Zoological Nomenclature validated the spelling "Argiope", on the basis that the change from the first to the second edition was an intended correction.

Species

As of April 2019, Argiope contains 88 species:

Representation of a Lie group

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/Representation_of_a_Lie_group...