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Diversity of Life

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Diversity of Life
Alessandro Minelli, University of Padua, Padua, Italy
Diversity of life (or biodiversity) is the variety of existing organisms, including their
diversity at the genetic level and the full range of ecological processes in which they
take part and of ecosystems to which they belong.
Why is Life so Diverse?
Article 2 of the Convention on Biological Diversity (the
so-called Rio Convention, 1992) defines biodiversity as
‘the variability among living organisms from all sources
including, inter alia, terrestrial, marine and other aquatic
ecosystems and the ecological complexes of which they
are part; this includes diversity within species, between
species and of ecosystems’. According to this definition,
three main levels of biological diversity can be identified:
genetic diversity, species diversity and ecosystem
diversity.
Genetic diversity is the heritable variation within a single
species, including the differences among individuals in a
local population. In an evolutionary perspective, this is the
ultimate source of all kinds of diversity in the biosphere. On
the other hand, ecosystem diversity is possibly the level of
biodiversity most obvious to the lay observer, because of
the immediate visual impact of the differences among
aquatic and terrestrial landscapes or vegetation types, such
as a pond and a seashore, a conifer forest and an alpine
meadow. However, its measurement suffers from major
problems of standardization. Most approaches to biolo-
gical diversity therefore focus on species (or taxonomic)
diversity; this operational choice will be followed in this
article.
A first-level explanation of the diversity of life on Earth
is the diversity of Earth itself. There are two major aspects
of geographical diversity of the physical environment that
allow living beings to become numerous. One aspect is
habitat heterogeneity at local, regional, continental and
even global scale. Organisms successfully thriving in a wide
spectrum of different habitats are rare, the bulk of living
species being instead confined, more or less strictly, to a
narrow set of environmental conditions. The physical
heterogeneity of the planet’s surface, however, does not
explain why similar habitats in different continents, and
even in different regions within the same continent, are
inhabited by widely dissimilar species. This is explained,
instead, by history. Physical or ecological barriers between
similar habitat patches may interrupt gene flow to such an
extent as to bring about allopatric speciation. Similar
habitats in individual islands within an archipelago or on
individual peaks within a rugged mountain range are
commonly inhabited by related but different species of
sedentary animals, such as land snails or wingless beetles.
ENCYCLOPEDIA OF LIFE SCIENCES / & 2001 Nature Publishing Group / www.els.net
Introductory article
Article Contents
. Why is Life so Diverse?
. History of Life
. Estimates of Current Diversity
All these species, whose geographic range may be restricted
to a few square kilometres, arose because of the physical or
ecological barriers that interrupted the genetic flow
between populations.
In oceanic archipelagos, this condition of geographical
isolation may affect the whole biota. For instance, the
native fauna and flora of oceanic islands such as the
Hawaiian chain is to a very large extent endemic: 89% for
angiosperms, 99% for insects. Moreover, within this single
island chain a large number of species are confined to one
single island, or even to a single district within one island,
due to the habitat fragmentation caused by local topo-
graphy or by recent lava flows. It has been estimated that
the more than 10 000 animal and plant species now
inhabiting the Hawaiian archipelago evolved there from
a few hundred successful colonizers, most of them of North
American origin.
The importance of geographical isolation in determining
high levels of species diversity is also apparent in a
comparison between marine and freshwater fishes. Of all
fish species described to date (some 25 000), those living in
the sea are less than twice as numerous as those living in
inland waters, although the total volume of oceanic waters
is about ten thousand times greater than the volume of
inland waters. The relatively enormous diversity of fresh-
water fish species is explained by the fact that inland waters
are fragmented into thousands of more or less completely
isolated basins, a condition largely facilitating allopatric
speciation.
In more general terms, it has been estimated that only
15% of all living species described to date inhabit the sea. It
is unlikely that future investigations will significantly alter
this ratio. Likely explanations of this unbalanced distribu-
tion of diversity include the higher heterogeneity of
continental environments and their higher structural
(architectural) complexity with respect to the conditions
prevailing in the oceans. At a higher taxonomic level,
however, animal life is more diverse in the sea than on land.
All animal phyla are represented in the sea and several
phyla (e.g. echinoderms, ctenophores, sipunculans, bra-
chiopods) are exclusively marine. This may be due, in part,
to the fact that life originated in the sea and remained
confined to this realm during much of its history; no less
important, however, is the effect of the strict adaptations
required for living in terrestrial (and, to a lesser degree,
freshwater) environments, adaptations that cannot be met
1
 Diversity of Life
by animals with body designs like those of a sea urchin or a
jellyfish.
A second major explanation of the diversity of life is
found in the multiple adaptations developed by most living
beings in relation to the other organisms with which they
interact, be these competitors, prey, predators, hosts or
symbionts. The relevance of these interactions for the
evolution of biological diversity is particularly conspic-
uous when two species interact so closely that each of them
represents a major selective agent in the evolution of the
other, thus offering a case for coevolution. Interesting
examples of coevolution are found in the relationships
between flowering plants and their insect pollinators: in
many instances, the two partners are so closely specialized
that size and shape of the insect’s mouthparts, temporal
flight schedules etc. are strictly matched by the shape of the
corolla, the location of the nectaries, the length and shape
of the stamens, and the timing of flower opening. Large
plant families such as orchids (around 18 000 species) and
legumes (around 16 500 species), and large genera such as
Ficus (figs; around 800 species), owe much of their
conspicuous species richness to their strict interactions
with specialized pollinators.
Interspecific relationships are also crucial in explaining
the astonishing diversity found in several groups of
parasites. Most parasites attack a very restricted number
of host species, sometimes just one. This explains, for
example, the remarkable diversity found in Eimeria, a
genus of sporozoan protists: more than one thousand
species have been described to date and it has been
estimated that in this genus there may exist some 35 000
species, each of them attacking a selected group (mostly a
genus, or even a single species) of vertebrate (rarely
invertebrate) hosts. The same will possibly apply to other
groups of parasites, e.g. to several families of nematodes.
A similar degree of host specificity is often found in small
animals (many groups of insects and mites) and fungi
(especially rusts, Puccinia and relatives) living on flowering
plants. Adaptations to their hosts involve these parasites’
specializations to exploit only selected parts of the host
plant, e.g. young leaves, mature leaves, stem, roots, seeds
etc., so that many dozen parasite species may attack the
same host without directly interacting with each other.
We must acknowledge, however, that neither geogra-
phical isolation nor specific adaptations to other organ-
isms can help explain those extraordinary instances of
biological diversity that are commonly known as species
flocks. These are groups of dozens and even hundreds of
species, all clearly derived from a single common ancestor
from which they diversified without perceptible geogra-
phical isolation and now all living in the closest geogra-
phical proximity within a restricted geographical area. The
most species-rich and best investigated species flocks are
those of the African cichlid fishes living in three large
freshwater basins, Lake Victoria, Lake Tanganyika and
Lake Malawi. Each of these lakes hosts a few hundred
2 ENCYCLOPEDIA OF LIFE SCIENCES / & 2001 Nature Publishing Group / www.els.net
different cichlid species, each of them with its strikingly
different morphological, ecological and behavioural adap-
tations, living alongside its closest relatives inhabiting the
same lake. In the case of Lake Victoria, the cichlid species
flock developed from a single ancestor since the last
dramatic desiccation of the whole basin dated c.12 000
years ago, a very short time span to account for the origin
of some three hundred species from a single ancestor.
As insects represent more than one half of the total
biological diversity on Earth, it is sensible to ask the
question, why are insects so numerous? A first explanation
of their unique diversity is to be found in their size. Insects
cannot be more than a few centimetres across, due to
structural constraints such as the mechanical properties of
their exoskeleton and the efficiency of gas diffusion in their
tracheal system; on the other hand, their complex
architecture cannot be easily accommodated in much less
than 1 mm length. In fact, most insects are between 1 and
20 mm long. Insects not being individually too big, do not
require large areas for populations to establish themselves,
therefore no long-distance displacements are generally
necessary for either feeding or reproduction. On the other
hand, most insects are either too heavy or too fragile for
long-distance passive transport. These conditions facilitate
the establishment of isolated populations, a prerequisite
for allopatric speciation. A second major cause of insect
diversity is their feeding specialization. This is true for
phytophagous species as well as for those living as
parasitoids of other arthropods. In both cases, high degrees
of host specificity are quite common.
History of Life
A few major events punctuated the history of life on Earth.
Some of these events were more or less particularly
instrumental for the resulting biological diversity. For a
couple of billion years (roughly speaking, 3000 to 1000
million years ago), life was represented only by prokar-
yotic, mostly unicellular forms, later accompanied by the
first, still unicellular, eukaryotes. Within this long time
span, two evolutionary transitions proved to be of
fundamental importance for the subsequent history of
biological diversity: the origin of sex, with which it becomes
meaningful to speak of biological species, and, later, the
origin of multicellularity, a prerequisite for the evolution of
complex and potentially diverse body plans such as those
of animals and plants. The few multicellular organisms
found in rocks older than one billion years are simple algal
threads composed of chain-linked single cells.
The first unequivocal metazoan-type fossils are those of
the Vendian or Ediacaran age, c.620 to 550 million years
ago. Their genealogical relations to modern phyla,
however, are much disputed. According to some palaeon-
tologists they represent an early, independent experiment

in multicellularity, not belonging to the ancestry of the true
metazoans. These true metazoans suddenly appear at the
base of the Cambrian strata, c.550 million years ago, in
what has been described as the Cambrian explosion of life.
Whether this stratigraphic evidence actually records an
abrupt rise in biodiversity or merely the consequence of the
development of the first mineralized (fossilizable) skeletons
is still a matter of dispute. However, this Cambrian event is
the single most dramatic event in the history of biodiversity
documented in the fossil record.
The Cambrian explosion was soon followed by the
diversification of the marine biota into four main
components: the infauna living within soft substrates,
the epifauna living at the surface of soft and especially
hard substrates, the plankton and, somehow later, the
necton, that is the complex of actively swimming animals,
many of them predators, including fishes and large
arthropods such as the eurypterids. Most Recent animal
phyla were already present in the Cambrian, some of them
(e.g. arthropods) with a great number of different species
and body plans.
A further crucial event in the history of life was the
invasion of land by plants (Middle Silurian), arthropods
(Upper Silurian) and vertebrates (Upper Devonian).
Plants colonized terrestrial habitats by developing rigid
stalks bearing photosynthetic leaves and reproductive
organs, a root system to anchor the stem and a vascular
system to conduct water and minerals; terrestrial animals
modified body surface and respiratory organs in order to
keep water loss to a minimum. The limited availability of
water also caused both plants and animals to adopt new
reproductive strategies.
Animals were obliged to abandon external fertilization
and to adopt spermatophores or to evolve internal
fertilization. The susceptibility to desiccation of eggs and
embryos was prevented either by laying the eggs in water
(thus retaining, or developing anew, an amphibian life
style), or otherwise. Many insects developed ovipositors to
lay eggs in living plant tissue, but the two definitive answers
to the danger of desiccation were found later, either in
viviparity or in the production of better encased eggs, such
as those of amniote vertebrates. In parallel, flagellated
male gametes requiring water to travel to the female
gametes were abandoned by the evolutionary line leading
to the flowering plants. The transition to land opened
enormous scope for a new diversification of life, because of
the physical discontinuities so widespread on the land
masses and the speciation facilitating opportunities (inter-
specific relationships) mentioned in the previous section.
Arachnids and myriapods were already present in the
Upper Silurian, whereas the oldest record for insects only
dates from the Lower Devonian, and the other major
group of nonmarine invertebrates, the pulmonate snails, is
only known from the Carboniferous. More or less at the
same time (end of early Carboniferous) insects had
developed flight ability.
ENCYCLOPEDIA OF LIFE SCIENCES / & 2001 Nature Publishing Group / www.els.net
Diversity of Life
Vertebrates came a bit later on the scene than
arthropods. The earliest known land-dwelling vertebrates
or tetrapods date from the Upper Devonian and the
earliest flying vertebrates did not evolve before the late
Triassic. These were pterosaurs, later to be joined by birds,
in the late Jurassic, whereas the first flying mammals (bats)
did not evolve before the Eocene. By that time, however,
most Recent orders of mammals had already differentiated
from mammal origins in the late Triassic.
A latecomer to the evolutionary scene are the angios-
perms, the earliest fossil evidence for this group only
dating from the early Cretaceous. Following this late
appearance, however, the flowering plants experienced a
rapid burst of differentiation, largely triggered by the
simultaneous explosion of insect diversity. The Palaeo-
gene was the time of origin of grasses (Gramineae), a plant
family whose enormous success is due largely to their
habit of continuous growth. Finally, the Neogene was the
age of herbaceous plants with the explosion of families
such as the Compositae (daisies and sunflowers), but also
of the passerine birds, whose diversification is probably
related, on one hand, to the diversification of seed-bearing
plants and, on the other hand, to their frequent
specialization to chasing flying insects. Other groups that
gently increased in diversity during the Neogene include
frogs and snakes.
The history of biological diversity, however, is not just
one of uninterrupted increase, it was also punctuated by
some major critical events known as mass extinctions.
One of the major mass extinctions happened towards the
end of the Devonian. Apparently, it did not affect the
vascular plants which had already placed their foot on
land, but in the sea it had catastrophic consequences on the
reef communities and affected with particular severity
trilobites, ammonoids, brachiopods and placoderms.
The most severe of all mass extinctions, however, was
probably the event that marks the end of the Permian (and
of the Palaeozoic era), when 70 to 90% of marine
invertebrate species became extinct within a short time
span. Whole previously successful groups such as trilo-
bites, tabulate and rugose corals and fusulinid foramini-
fera disappeared completely; others, such as brachiopods,
bryozoans, ammonoids and the stalked echinoderms, were
severely affected.
The next major event was the K–T extinction, at the
boundary between the Cretaceous and the Tertiary. This
is the most widely investigated extinction, marked by the
disappearance of two well-known and very diverse
groups, the ammonoids and dinosaurs. Other groups
that went extinct by the end of the Cretaceous include
two groups of large aquatic reptiles, the plesiosaurs
and the mosasaurs, and the rudists, a family of large
reef-building bivalves with heavy, odd-shaped
shells. The K–T extinction also severely affected the
planktonic realm, especially foraminifera, radiolarians
and coccolithophores.
3
 Diversity of Life

Estimates of Current Diversity biological species concept, these living beings simply
demonstrate that not all aspects of life are articulated in
The single most commonly used descriptor of species a biological species; this would imply that describing
diversity is species number. This number is correlated, biodiversity only in terms of species counts is, in principle,
indeed, with some measures of ecological diversity, such as unsatisfactory.
the complexity of food webs, or topographic diversity. An estimate of the number of species named to date is
However, species richness is, at best, just a measure of one given in Table 1.
aspect of the global diversity of life. From a geographical point of view, there are some
To improve the information content of biodiversity prominent hot spots of biological diversity. For example,
estimates, it has been suggested that we need to incorporate the four areas of highest diversity for higher plants are
measures of phylogenetic relatedness among the species Latin America, where one-third of the world flora is at
present in a given area, so to approach a more informative home with some 85 000 species thus far recorded, China
description of ‘character richness’ in the sample. (30 000 species, some 12% of the world total), Mexico
But even estimating species diversity on Earth is not (26 000) and Indonesia (20 000).
easy. This is due only in part to the incompleteness of our A latitudinal gradient of biodiversity, with species
current inventory of biodiversity. There are serious number decreasing from the Equator to the Poles, is
problems, indeed, even with that part of biological broadly observable despite the existence of many plant and
diversity that has been already described and named. A animal groups whose distribution is centred in the
first problem arises because of the lack of comprehensive temperate areas, such as the Rosaceae, the Cruciferae
and reliable monographs for many, if not most, of the and the aphids. These latitudinal differences in species
major groups of living beings. For example, there is no diversity are observed at the local as well as at the regional
recent world catalogue for popular groups such as beetles level. For instance, on one hectare of tropical forest in
(Coleoptera), or butterflies and moths (Lepidoptera): that Ecuador there may be as much as 473 tree species, whereas
means that the current estimates of 400 000 described in a temperate forest a mere handful of tree species (if not
species in the first group and 150 000 in the second may well just one species, as in many forest stands in cold temperate
be some 20% wrong. The major difficulty is not so much areas) may cover hundreds of square kilometres. Historical
retrieving all existing species names from a very scattered factors as well as present-day conditions concur to the
literature, but identifying all synonymies; that is, all cases explanation of the higher species diversity in the tropics.
where two or more different names apply to one and the For instance, it has been suggested that during the
same species. Synonymization requires a critical appraisal Pleistocene the Amazonian forest became fragmented into
of old and new evidence and, as such, requires the time- a large number of small areas that acted as refugia for the
consuming work of many dedicated specialists. Even for a forest fauna and provided opportunity for intensive
well-researched group such as the flowering plants, less allopatric speciation. Later on, when these forest frag-
than 20% of the currently recognized species have been ments joined together again to form the present-day forest,
treated in genus- or family-level monographs during the the species that had differentiated in the separate refugia
twentieth century. had a chance to expand and to become sympatric. How
A more subtle but far from trivial problem derives from
the uncertainties in the definition of the basic unit of Table 1 Estimated number of species named to date
biodiversity. The circumscription of species may be very
different, indeed, if one adopts a biological or a phyloge- Existing
netic species concept. This is well exemplified by a 1992 Described (working figure)
study of the birds-of-paradise, a well-known group where ( 103) ( 103)
traditional classifications, based on the biological species
Bacteria 4 1000
concept, acknowledge the existence of 40 to 42 species,
Fungi 75 1000
whereas not less than 90 phylogenetic species may be
‘Protozoa’ 40 300
distinguished in the same group. Still worse is the case of
‘Algae’ 45 400
organisms with uniparental reproduction, where the
Land plants 270 300
biological species concept simply does not apply, by
Nematodes 25 500
definition. Examples are offered, in the northern temperate
Crustaceans 45 150
regions, by the brambles (Rubus), the hawthorns (Cratae-
Arachnids 80 750
gus) and the dandelions (Taraxacum). In each of these three
Insects 1000 10 000
genera, hundreds of species names have been given to
Molluscs 100 200
slightly different morphotypes, which are perhaps mor-
Chordates 50 55
phologically distinct, but often, occurring together in the
Others 130 300
same spot, do not behave as different ecological units
Total  1900  15 000
within the local community. For the strict advocates of the

4 ENCYCLOPEDIA OF LIFE SCIENCES / & 2001 Nature Publishing Group / www.els.net


much their present coexistence depends on the high
complexity of the ecosystem or on its high productivity is
still matter for dispute.
The current level of knowledge varies greatly between
different groups. In the case of birds, if we disregard the
problems arising from adopting different species concepts,
we can reasonably expect that no more than a few dozen
species remain to be described. In the case of mammals,
however, recent descriptions of previously unknown
species are not limited to small inconspicuous species of
rodents, shrews and bats, but also include, quite unexpect-
edly, some large animals such as the bilkis gazelle (Gazella
bilkis) from Yemen, described in 1985, Madagascar’s
golden lemur (Hapalemur aureus), described in 1986, and
four large ruminants from the Vietnamese forests, three of
them representing completely new genera, first described in
the 1990s: the saola or spindlehorn (Pseudoryx nghetin-
ghensis), the linh duong (Pseudonovibos spiralis), a giant
muntjac deer (Megamuntiacus vuquangensis) and another
muntjac (Muntiacus truongsonensis).
It is for invertebrates, however, that a truly dramatic
increase in species description has taken place in the last
few decades. An impressive example is provided by
arachnids and crustaceans: in these groups, the number
of new species described between 1960 and 1970 equals the
total number of species described in the same groups
during the previous two centuries. This example easily
suggests that a large percentage of existing species have not
yet been described.
Currently, at least 15 000 species are annually described
as new.
Different approaches have been followed to obtain
estimates of the number of existing species. These methods
generally focus either on less intensively investigated
taxonomic groups, such as bacteria, fungi, nematodes,
mites and insects, or on some exceptionally species-rich
habitats. The two aspects, however, are closely inter-
related. For example, insects are the main component of
species diversity in the tropical forest canopy, as nema-
todes are in the deep sea floor.
A sample of arthropods collected on just 10 trees in
Borneo included 24 000 specimens, belonging to more than
2800 species. One of the most abundant and diverse groups
were the tiny parasitic chalcid wasps: among the 1455
specimens belonging to this group, 739 different species
could be counted, 437 of these being represented by just
one specimen each. These and similar data have led to an
estimation of the total number of arthropod species in the
tropical forests worldwide at somewhere between 10
million and 80 million. Much more conservative estimates,
however, have been obtained following different ap-
ENCYCLOPEDIA OF LIFE SCIENCES / & 2001 Nature Publishing Group / www.els.net
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Diversity of Life
proaches. It may be sensible, for instance, to compare the
number of described and undescribed species collected by
prolonged sampling efforts in biologically rich and hitherto
less investigated areas. Thus, in a very extensive collection
of Hemiptera from a topographically diverse area of
tropical rainforest in Sulawesi (in Indonesia), the described
species amounted to more than one-third of the total, thus
suggesting that the total number of extant species of the
same group, and of insects at large, would only be round
2.5 million, i.e. less than three times the figure for the
species described thus far.
Besides the tropical forest canopy, possibly the richest
reservoir of uncharted biodiversity is the deep-sea, despite
the relatively low amount of energy flowing through it.
Estimating this aspect of biodiversity, however, is even
more problematic than in the case of tropical insects.
Global estimates of existing biodiversity are thus quite
uncertain. Figures ranging from 5 to 130 million species
have been recently offered for the gross total. Those given
in Table 1, although quite subjective, are only slightly higher
than the working figures most often offered in the
literature.
Species counts are the simplest but not the only possible
way of describing biodiversity at either local or regional
level. Interesting comparisons between ecosystems may be
obtained, for instance, by considering the local distribu-
tions of species in terms of the average size of adult
individuals or in terms of relative or absolute abundance of
the species.
Further Reading
Briggs DEG and Crowther PR (eds) (1990) Paleobiology: a Synthesis.
Oxford: Blackwell Scientific Publications.
Forey PL, Humphries CJ and Vane-Wright PJ (ed.) (1997) Systematics
and Conservation Evaluation. Oxford: Oxford University Press.
Gaston KJ (ed.) (1996) Biodiversity: a Biology of Numbers and
Difference. Oxford: Blackwell Science.
Groombridge B (ed.) (1992) Biodiversity: Status of the Earth’s Living
Resources. London: Chapman and Hall.
Harper JL and Hawksworth DL (1994) Biodiversity: measurement and
estimation. Philosophical Transactions of the Royal Society of London,
B 354: 5–12.
Heywood VH and Watson RT (eds) (1995) Global Biodiversity
Assessment. Cambridge: Cambridge University Press.
Hochberg ME, Clobert J and Barbault R (eds) (1995) The Genesis and
Maintenance of Biological Diversity. Oxford: Oxford University Press.
Maynard Smith J and Szathmáry E (1995) The Major Transitions in
Evolution. New York: Freeman.
Minelli A (1993) Biological Systematics: the State of the Art. London:
Chapman and Hall.
Reaka-Kudla ML, Wilson DE and Wilson EO (eds) (1997) Biodiversity
II. Washington DC: Joseph Henry Press.
5