In the sciences of alive the, the species is the unit, or Taxon basic of the Systématique. Its definition differs according to the disciplines:
The Taxon (kind, species, etc) is the entity which is supposed to gather all the organizations having jointly certain characters Taxinomique S or diagnostic, considered homogeneous according to the level, or Rang taxinomic. This taxon is defined by:
The scientific names “are famous Latin S” and are written in Italique. When one refers to a nongiven species (not identified) but whose kind is known, it is of use to use as provisional epithet the abbreviation of species , “ Sp. ” in the singular (and “ Spp. ” in the plural) following the name of kind; in the same way, “subspecies” is shortened in “ Ssp. ” in the singular (and “ Sspp. ” in the plural). These abbreviations are written in Roman characters .
Since the advent of the theory of the evolution, the concept of species biological appreciably evolved/moved, but no consensus could be obtained on its definition.
The definition most commonly quoted is due to Ernst Mayr. According to this definition, which is that of the concept of species biological (or isolated species), the species are “groups of Population S Naturelle S, indeed or potentially interfécondes, which is genetically isolated from other similar groups”. But as one as well finds reproduction asexual (or a parthenogenesis) in the animals as at the plants and in almost all the groups of animals (fish, reptiles, batrachians, insects), the concept of species cannot be related to the interfertility any more.
Many other definitions also have course for example the species can be defined as a population whose members can cross without difficulties under conditions Naturelle S.
Another definition rests on the concept of resemblance (or contrary to degree of difference), concept still very much used in Paléontologie, where there is not an other option. Certain authors use even these two principles to define the species.
The study of DNA nowadays makes it possible to seek nonvisible resemblances directly on the physical level (Phénotype). But the quantitative criterion (many identical genes) mask the qualitative criterion, by nonmeasurable definition. Thus, the classification of the Orchises of the Ophrys type emphasizes a great number of species, obviously different (thus from the point of view Phénotype) whereas their Génotype S appeared very close.
The biological species is generally defined today like a reproductive Communauté (interfecondity) of populations. If this definition lends itself rather well to the Animal kingdom, it is less obvious in the Vegetable kingdom, where frequently occur Hybridation S. One often associates the double criterion of meeting by Interfécondité and separation by non-interfecondity, to ensure the perpetuation of the species.
A question deserves to be posée : does the concept of species constitute a simple convenience of work or it has a reality independent of our system of classification ? Does it have a true significance in the absolu ? The species to which laws are universally applicable, or has a logical class same reality as an individual (by chalk-lining)? The answers to these considerations concern the epistemology and the operational Sémantique as much as Biologie.
The problem becomes complicated because of the questions of interfecondity present or goes away, and not always as distinct as in the manuels : populations A1, A2 can be interfécondes, like A2 and A3…. and An-1 and An and one can have at one time of the populations A1 and An which is not (it is to it case of variation clinale or species boxing ring which is brought back by Konrad Lorenz at the seagulls . The concept of species then dissolves in a kind of fuzzy).
The interfecondity thus does not make it possible to say that they are same species while the non-interfecondity is enough to say that they are different species. This non-interfecondity must be also and especially required in the descendants : horses and asses are interféconds but their hybrids (mule and mule, shingle or bardot) are it seldom. The two populations thus form different species.
In the same way, certain races of dogs ( Canis familiaris ) are hybrident without problem - and have a fertile descent - with common wolves ( Canis lupus ), while their hybridization with other races of their own species Canis familiaris remains quite problematic - in the case for example of a Chihuahua female and a Saint-Bernard  male;!
That is explained by two faits : the domestic dog is very polymorphic and it is an artificial selection starting from wolves - there is now genetic evidence. One should thus name it Canis lupus familiaris , i.e. a subspecies of the Wolf thus perfectly interfécond with him… within the limit of what allows physically the receiving uterus.
Empirical concept, the concept of species evolved/moved with time and its history was marked by the thought of large naturalists like Linné, Buffon and Darwin.
Initially, one regarded the species as fixed entities defined by morphological criteria. This typological design found its apogee with work of Linné and the establishment of collections of individuals “ typiques ” of the species.
a species is thus a simple chalk-lining which has its own evolutionary tendencies and its own historical destiny (according to Delforge P Guide of the Orchises of Europe… Delachaux and Niestlé 1994). Concept of “ Destiny ” no base scientifique  has;: “its own history” not only would be appropriate well better but moreover, it is what seek to discover number of scientifiques ! The concept of “simple chalk-lining” must also be moderate because, as one saw, a certain interfecondity remains possible between certain species proches : it can result from it from the fertile descendants to the characteristics more adapted to their medium which will perhaps form with time a species with whole share.
At the end of a certain time, this group of individuals takes specific characteristics which differentiate it from the species of reference. These characters can be new (appearance following a change for example) or be the fixing of a variable characteristic at the species of reference.
Different subspecies often have the possibility of reproducing between them, because their differences (still) are not marked.
The rules of the Nomenclature want that, the first time that a species is divided into subspecies, the subspecies which corresponds to the specimens which were used to describe the “standard” species, takes a second of the same epithet automatically name than that of the species. This trinomial is known as autonomous (or nominal ), because it does not require the publication of a new diagnosis.
Thus, in Zoologie the subspecies of reference of Tarentola mauritanica will be indicated under the name of Tarentola mauritanica mauritanica each time one needs to distinguish it. The other subspecies (which will have to be the subject of a description validly published) will have an obligatorily different final epithet: for example Tarentola mauritanica fascicularis .
Since approximately 1960, one uses more and more designation “ formed ”, shortened “ F. ”, which expresses clearly that it is about the shape of pet which can possibly go up to various wild subspecies: Capra aegagrus F. hircus .
In Botanical and Mycology, the two epithets after the name kind must be separated by the shortened indication of the row (cut) infraspecific: Subsp. or Ssp., VAr. or V., Fo. or F., respectively meaning subspecies, varietas and formed . For example: ''Agaricus bisporus'' fo. ''bisporus'' .
The row of form (fo.) will be used to indicate an entity of row lower than the species and the variety. The form being the smallest taxinomic cut in the Systematic and the Classification of the alive world, nearest to the “involved individual”. For example, when we say that we have in our plate the “white form” of the Cultivated mushroom , we make same division empirically as the mycologist who named it by the Trinôme Agaricus bisporus fo. alba .
More still than the varietal row, the choice of the formal row indicates that the population of individuals thus circumscribed differs from the “standard” species only by one or more characters considered as minor on a plan taxinomic (morphological characteristic , ecological, Organoleptique, etc), like the “white color” in our example. One can wonder about the validity of the definition of a subspecies knowing that the definition of the term species remains fluctuating and discussed. It is the same here and all the limits of the definition of a species also apply for that of a subspecies.
Whereas one estimates at approximately 13-14 million the number of alive species on planet, only a tenth (pilot of the difficulties related to the concept of species, the number itself of described species remains vague, between 1,5 and 1,8 million) was described scientifically.
The great majority of the not described species are Procaryote S (Archea and Eukarya) and unicellular Eucaryote S, Protozoaire S like the Algue S, certain ex-mushrooms now classified in the Straménopiles, or of the Myxomycètes (now classified in several groups of protists…).
In 2006, according to the red List of the UICN, the identified species can be broken up as follows:
287,655 Plant S, of which:
Approximately 10.000 new species are described each year. It is which also disappears because of man (see Dodo, genetic Diversité…), and others finally eliminated by climate changes from the niche where they lived.
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