There are different ways in which objects can be classified and the human mind is very good at generating criteria for classification. This is why the following list, assembled by the Argentinean author Jorge Luis Borges, and purportedly extracted from an ancient Chinese encyclopedia (Lakoff 1987), strikes us as funny:
“…it is written that animals are divided into:
·
those
that belong to the Emperor;
·
embalmed
ones;
·
those
that are trained;
·
suckling
pigs;
·
mermaids;
·
fabulous
ones;
·
stray
dogs;
·
those
that are included in this classification;
·
those
that tremble as if they were mad;
·
innumerable
ones;
·
those
drawn with a very fine camel’s hair brush;
·
others;
·
those
that have just broken a flower vase;
·
those
that resemble flies from a distance.”
The two major criteria that are used to classify things (neither met by
Borges’ list), are utility or affinity:
·
Utility
generates
classifications whose objects are easy to
find. An example of such a classification would be a dictionary, whose
entries are arranged alphabetically;
·
Affinity,
on the other hand generates classification wherein adjacent objects are
straightforward to compare (because
adjacent entries share important features).
In the European middle ages, animal books (‘Bestiarum’) were usually ordered alphabetically. However, such
ordering eventually struck people as odd, especially as people realized, in the
course of long debates on ‘universals’ (on whether names are ‘natural’
attributes of things, or not), that names are arbitrary labels.
Thus, authors gradually began seeking for natural classifications,
wherein organisms are ordered by affinities, these affinities being initially
conceived as reflective of the general rules which god used when creating these
organisms.
The work of Linnaeus, whose Systema
Naturae, the tenth edition (1758) of which still marks the beginning of
zoological nomenclature, is an example of such attempts to identify the
underlying affinities among plants and animals. The resulting ‘natural’
classifications have started to make sense, however, only since Darwin, in The
Origin of Species (1859), provided a rationale for affinities, that is,
shared ancestry. However, Darwin not only provided a basis for the affinities
between organisms. He also provided a mechanism by which new species and higher
taxa emerged out of common ancestors. This mechanism he called natural
selection.
Natural selection is the core of Charles Darwin’s work and is best
defined in his own terms: “many of every
species are destroyed either in egg or [young or mature (the former state the
more common)]. In the course of thousand generations infinitesimally small
differences must inevitably tell; when unusually cold winter, or hot or dry
summer comes, then out of the whole body of individuals of any species, if there
be the smallest differences in their structure, habits, instincts [senses],
health, etc., <it> will on an average tell; as conditions change a rather
larger proportion will be preserved: so if the chief check to increase falls on
seeds or eggs, so will, in the course of 1,000 generations, or ten thousand,
those seeds (like one with down to fly) which fly furthest and get scattered
most ultimately rear most plants, and such small differences tend to be
hereditary like shades of expression in human countenance” (Darwin 1842).
Natural selection, thus, consists of three elements:
·
organisms
usually produce far more progeny than their habitat can accommodate;
·
each
member of the progeny differs in some inheritable
attributes or properties;
·
there is
a tendency for those progeny with attributes or properties that are more
suitable for the habitat in question to suffer a lower rate of mortality and
thus for more of them to reach reproductive age than their sibling.
These three features jointly cause animals and plants, over evolutionary time, to ‘track’ fluctuation of their environment. In this process, and in conjunction with other mechanisms such as the ‘founder effect’ and the effect of neutral selection, isolated populations can become so different from the mother species that their members will not be able to cross-mate if the barrier that once separated them disappears.
Species are “groups of actually (or potentially) interbreeding natural populations which are reproductively isolated from other such groups” (Mayr 1942, p. 120).
Since species are the basic rank of biological nomenclature, naming
species is very important and we now follow for this a model proposed by
Linnaeus (see above), wherein the species is defined by a so-called binomen
consisting of a unique genus name, always starting with a capital letter, and a species
epithet
, which is never capitalized; usually, both are written in italics. With
regard to the capitalization rule, simply recall that the binomen is the short
version of an earlier mode of description wherein a whole paragraph was used to
describe, and thereby define, a species. The binomen, thus, was the start of a
sentence.
Important additions to a species name are the name of the author who
first described a species and the year of that description; as in, for example,
the Linnaean species Salmo
trutta Linnaeus, 1758. At times you will
encounter a species, e.g. Oncorhynchus
mykiss, with an author’s name and year in
brackets, e.g. (Walbaum, 1792). This means that the species whose epithet is mykiss
was originally described as a member of another genus, in this case Salmo.
However, due to better understanding of its relationships with other trout and
salmon species, was subsequently moved into the genus Oncorhynchus.
Another rule important to animal species names are that the genus part
of the name must be unique to the animal kingdom. From the year 2000 on, it must
also be unique among all organisms. Thus, when a generic name is coined,
the author must verify that this name has never been used by any other
zoologist, and, from 2000 on, by any botanist, bacteriologist, etc. This
seemingly daunting task is not impossible. Global catalogues of organism names
are now being created; the most important of these is the Species 2000 catalogue
(see www.sp2000.org).
Given the mechanism of natural selection, every fish population
can be conceived as being a potential new species. All one needs to imagine is
that populations become isolated from others long enough for their members to
lose the ability to mate with those of other populations. However, as long as
some members of each population continue to mate with members of other
populations of the same species, a mating barrier will not emerge (only a small
gene flow is required to prevent the emergence of a mating barrier). Thus
populations, though they may be easy to define them in terms of attributes such
as number of scales or spines or body proportions, should not be given full
taxonomic status, because (contrary to species) they usually do not maintain
themselves over a long period. Not having taxonomic status also means they
should not have formal names, such as the trinomen
that are still frequently used today, e.g. Oreochromis
niloticus niloticus.
The third part of the trinomen refers to a subspecies, which is, in fact, a
population, or, to use a term much used in earlier times, a ‘race’.
Species differ as to the extent of their diversity. Some species consist of a single population of a few individuals — these are often endangered species. Others have wide ranges and a rich population structure. This situation tempted authors to name subspecies. However, its is usually not objectively defined within-species diversity which has motivated authors to define subspecies, but national or local research traditions, and the resources available for sampling specimens over large areas, and curate them. Thus, Berg (1965) established numerous subspecies and even lower taxa for the fishes of adjacent lakes and rivers of the former Soviet Union, while subspecies are rarely proposed by taxonomists working on the many coral reef species of the Indo-Pacific, although their distribution spans thousands of kilometers, and detailed studies may justify this (at least if one believes in naming subspecies).
The common
names
of fish are what most people know about most fish. Thus, capturing the common
names of fish in various languages captures most of what people who speak these
languages know about fish. For this reason, FishBase includes over 100,000 names
of fish in over 100 languages, ranging from widespread languages such as English
or Spanish, to languages spoken by few speakers, such as Haida in Haida Gwaii,
British Columbia. Anthropologists, notably Berlin (1965), have established that
essentially all ethnic groups in the world spontaneously differentiate a similar
number (about 500) of ‘kinds’ of organisms, the kinds roughly corresponding
to genera, with important species being named, as well as some of their life
history stages.
The sounds in fish names also generate interesting patterns. Thus, small
fishes (i.e., fishes with small values of Lmax)
tend to have names containing high pitch sound such as ‘i’ or ‘ee’,
while large fish tend to have names with lower pitch sounds, such as ‘a’, or
‘aa’ (Berlin 1992; Palomares et al. 1999).
Tasks for the student:
· Look at the scientific names of ten species whose author name is in brackets and identify for each the original name and several synonyms. List and define the different kinds of synonyms.
· Identify a language with at least 50 different names in FishBase. Relate the number of species with i/ee sounds in their names against the maximum length reported for those species, i.e., test the occurrence of a sound-size association for fish in the language in question. [Hints: use the Information by country/island search to get a list of common names (and the corresponding scientific names) by language; get maximum size information from the Species Summary page and see item (5) of www.fishbase.org/Tips.htm on how to export data to a spreadsheet (Excel format) for further analysis.]
Classification-related topics covered in FishBase:
| FishBase: | To search for terms included in the FishBase online glossary, go to www.fishbase.org/search.cfm and use the Glossary search by either typing in a term or browsing the index provided. Note that here, and for nearly all other terms in the glossary, you can click on the hypertext link to the Encyclopedia Britannica online. |
| Classification: | The Role of Taxonomy; The FAMILIES Table; Genera and Species in a Classification |
| Darwin, Charles: | See Box 9 in The Expeditions Table |
| Species concept: | Eschmeyer's Genera of Fishes; Eschmeyer's Species of Fishes |
| Go to www.fishbase.org/search.cfm, use the Scientific name search either by typing in the genus and species names or by browsing the provided index and select the Summary button. In the Species Summary page, click on the Synonyms link, e.g., Oncorhynchus mykiss | |
| Subspecies: | The STOCKS Table |
| Go to www.fishbase.org/search.cfm and search for Oreochromis niloticus niloticus | |
| Population: | The STOCKS Table |
| Threatened species: | See Status field in The STOCKS Table |
| Go to www.fishbase.org/search.cfm, use the Information by country/island search, type in the country of interest and select the Threatened button. | |
| Common names: | See Fig. 8 in The COMMON NAMES Table |
| Go to www.fishbase.org/search.cfm and use the Common name search by typing in the name or by browsing the provided index. If a list of species is returned, click on the species of interest to access the Species Summary page. Then click on the Common names link, e.g., click on the Haida name ‘Skaagwun’ | |
| Max. length (Lmax): | The POPCHAR Table |
| Go to www.fishbase.org/search.cfm to search for a species as described above. Once in the Species Summary page, click on the Max. age & size link to obtain a list of maximum lengths, e.g., Salmo trutta | |
| See also Life-history tool example for Growth and Life span in Chapter 3. |