Plants are mainly
multicellular organisms, predominantly
photosynthetic eukaryotes of the
kingdom Plantae. Historically, plants were treated as one of two kingdoms including all living things that were not
animals, and all
algae and
fungi were treated as plants. However, all current definitions of Plantae exclude the fungi and some algae, as well as the
prokaryotes (the
archaea and
bacteria). By one definition, plants form the
clade Viridiplantae (Latin name for "green plants"), a group that includes the
flowering plants,
conifers and other
gymnosperms,
ferns and
their allies,
hornworts,
liverworts,
mosses, and the
green algae, but excludes the
red and
brown algae.
Green plants obtain most of their energy from
sunlight via
photosynthesis by primary
chloroplasts that are derived from
endosymbiosis with
cyanobacteria. Their chloroplasts contain
chlorophylls a and b, which gives them their green color. Some plants are
parasitic or
mycotrophic and have lost the ability to produce normal amounts of chlorophyll or to photosynthesize, but still have flowers, fruits, and seeds. Plants are characterized by
sexual reproduction and
alternation of generations, although
asexual reproduction is also common.
There are about 320,000
species of plants, of which the great majority, some 260–290 thousand,
produce seeds.
Green plants provide a substantial proportion of the world's molecular oxygen,
and are the basis of most of Earth's ecosystems. Plants that produce
grain,
fruit, and
vegetables also form basic human foods and have been
domesticated for millennia. Plants have many
cultural and other uses, as ornaments,
building materials,
writing material and, in great variety, they have been the
source of medicines and
psychoactive drugs. The scientific study of plants is known as
botany, a branch of
biology.
Definition
All living things were traditionally placed into one of two groups, plants and animals. This classification may date from
Aristotle (384 BC – 322 BC), who made the distinction between plants, which generally do not move, and animals, which often are mobile to catch their food. Much later, when
Linnaeus (1707–1778) created the basis of the modern system of
scientific classification, these two groups became the
kingdoms Vegetabilia (later Metaphyta or Plantae) and
Animalia (also called Metazoa). Since then, it has become clear that the plant kingdom as originally defined included several unrelated groups, and the
fungi and several groups of
algae were removed to new kingdoms. However, these organisms are still often considered plants, particularly in popular contexts.
The term "plant" generally implies the possession of the following traits: multicellularity, possession of cell walls containing
cellulose, and the ability to carry out photosynthesis with primary chloroplasts.
[– Definition from the Merriam-Webster Online Dictionary">]
Current definitions of Plantae
When the name Plantae or plant is applied to a specific group of organisms or
taxon, it usually refers to one of four concepts. From least to most inclusive, these four groupings are:
Another way of looking at the relationships between the different groups that have been called "plants" is through a
cladogram, which shows their evolutionary relationships. These are not yet completely settled, but .
Those which have been called "plants" are in bold (some minor groups have been omitted).
The way in which the groups of green algae are combined and named varies considerably between authors.
Algae

Algae comprise several different groups of organisms which produce food by photosynthesis and thus have traditionally been included in the plant kingdom. The
seaweeds range from large multicellular algae to single-celled organisms and are classified into three groups, the
green algae,
red algae and
brown algae. There is good evidence that the brown algae evolved independently from the others, from non-photosynthetic ancestors that formed endosymbiotic relationships with red algae rather than from cyanobacteria, and they are no longer classified as plants as defined here.
The Viridiplantae, the green plants – green algae and land plants – form a
clade, a group consisting of all the descendants of a common ancestor. With a few exceptions, the green plants have the following features in common; primary
chloroplasts derived from cyanobacteria containing
chlorophylls ''a'' and ''b'', cell walls containing
cellulose, and food stores in the form of
starch contained within the plastids. They undergo closed
mitosis without
centrioles, and typically have
mitochondria with flat cristae. The
chloroplasts of green plants are surrounded by two membranes, suggesting they originated directly from endosymbiotic
cyanobacteria.
Two additional groups, the
Rhodophyta (red algae) and
Glaucophyta (glaucophyte algae), also have primary chloroplasts that appear to be derived directly from endosymbiotic
cyanobacteria, although they differ from Viridiplantae in the pigments which are used in photosynthesis and so are different in colour. These groups also differ from green plants in that the storage polysaccharide is
floridean starch and is stored in the cytoplasm rather than in the plastids. They appear to have had a common origin with Viridiplantae and the three groups form the clade
Archaeplastida, whose name implies that their chloroplasts were derived from a single ancient endosymbiotic event. This is the broadest modern definition of the term 'plant'.
In contrast, most other algae (e.g.
brown algae/diatoms,
haptophytes,
dinoflagellates, and
euglenids) not only have different pigments but also have chloroplasts with three or four surrounding membranes. They are not close relatives of the Archaeplastida, presumably having acquired chloroplasts separately from ingested or symbiotic green and red algae. They are thus not included in even the broadest modern definition of the plant kingdom, although they were in the past.
The green plants or Viridiplantae were traditionally divided into the green algae (including the stoneworts) and the land plants. However, it is now known that the land plants evolved from within a group of green algae, so that the green algae by themselves are a
paraphyletic group, i.e. a group that excludes some of the descendants of a common ancestor. Paraphyletic groups are generally avoided in modern classifications, so that in recent treatments the Viridiplantae have been divided into two clades, the
Chlorophyta and the
Streptophyta (including the land plants and Charophyta).
The Chlorophyta (a name that has also been used for ''all'' green algae) are the sister group to the Charophytes, from which the land plants evolved. There are about 4,300 species,
mainly unicellular or multicellular marine organisms such as the sea lettuce, ''
Ulva''.
The other group within the Viridiplantae are the mainly freshwater or terrestrial Streptophyta, which consists of the land plants together with the Charophyta, itself consisting of several groups of green algae such as the
desmids and
stoneworts. Streptophyte algae are either unicellular or form multicellular filaments, branched or unbranched.
The genus ''
Spirogyra'' is a filamentous streptophyte alga familiar to many, as it is often used in teaching and is one of the organisms responsible for the algal "scum" on ponds. The freshwater stoneworts strongly resemble land plants and are believed to be their closest relatives. Growing immersed in fresh water, they consist of a central stalk with whorls of branchlets.
Fungi
Linnaeus' original classification placed the fungi within the Plantae, since they were unquestionably neither animals or minerals and these were the only other alternatives. With 19th century developments in
microbiology,
Ernst Haeckel introduced the new kingdom Protista in addition to Plantae and Animalia, but whether fungi were best placed in the Plantae or should be reclassified as protists remained controversial. In 1969,
Robert Whittaker proposed the creation of the kingdom Fungi. Molecular evidence has since shown that the
most recent common ancestor (concestor), of the Fungi was probably more similar to that of the Animalia than to that of Plantae or any other kingdom.
Whittaker's original reclassification was based on the fundamental difference in nutrition between the Fungi and the Plantae. Unlike plants, which generally gain carbon through photosynthesis, and so are called
autotrophs, fungi do not possess chloroplasts and generally obtain carbon by breaking down and absorbing surrounding materials, and so are called
heterotrophic
saprotrophs. In addition, the substructure of multicellular fungi is different from that of plants, taking the form of many chitinous microscopic strands called
hyphae, which may be further subdivided into cells or may form a
syncytium containing many
eukaryotic nuclei. Fruiting bodies, of which
mushrooms are the most familiar example, are the reproductive structures of fungi, and are unlike any structures produced by plants.
Diversity
The table below shows some species count estimates of different green plant (Viridiplantae) divisions. About 85–90% of all plants are flowering plants. Several projects are currently attempting to collect all plant species in online databases, e.g. the
World Flora Online and
World Plants both list about 350,000 species.
The naming of plants is governed by the
International Code of Nomenclature for algae, fungi, and plants and
International Code of Nomenclature for Cultivated Plants (see
cultivated plant taxonomy).
Evolution
The evolution of plants has resulted in increasing
levels of complexity, from the earliest
algal mats, through
bryophytes,
lycopods,
ferns to the complex
gymnosperms and
angiosperms of today. Plants in all of these groups continue to thrive, especially in the environments in which they evolved.
An algal scum formed on the land , but it was not until the
Ordovician Period, around , that land plants appeared. However, new evidence from the study of carbon isotope ratios in Precambrian rocks has suggested that complex photosynthetic plants developed on the earth over 1000 m.y.a. For more than a century it has been assumed that the ancestors of land plants evolved in aquatic environments and then adapted to a life on land, an idea usually credited to botanist
Frederick Orpen Bower in his 1908 book ''The Origin of a Land Flora''. A recent alternative view, supported by genetic evidence, is that they evolved from terrestrial single-celled algae, and that even the common ancestor of red and green algae, and the unicellular freshwater algae
glaucophytes, originated in a terrestrial environment in freshwater biofilms or microbial mats. Primitive land plants began to diversify in the late
Silurian Period, around , and the results of their diversification are displayed in remarkable detail in an early
Devonian fossil assemblage from the
Rhynie chert. This chert preserved early plants in cellular detail, petrified in volcanic springs. By the middle of the Devonian Period most of the features recognised in plants today are present, including roots, leaves and secondary wood, and by late Devonian times seeds had evolved.
Late Devonian plants had thereby reached a degree of sophistication that allowed them to form forests of tall trees. Evolutionary innovation continued in the Carboniferous and later geological periods and is ongoing today. Most plant groups were relatively unscathed by the
Permo-Triassic extinction event, although the structures of communities changed. This may have set the scene for the evolution of flowering plants in the Triassic (~), which exploded in the Cretaceous and Tertiary. The latest major group of plants to evolve were the grasses, which became important in the mid Tertiary, from around . The grasses, as well as many other groups, evolved new mechanisms of metabolism to survive the low and warm, dry conditions of the tropics over the last .
A 1997 proposed
phylogenetic tree of Plantae, after Kenrick and Crane, is as follows, with modification to the Pteridophyta from Smith ''et al.'' The
Prasinophyceae are a
paraphyletic assemblage of early diverging green algal lineages, but are treated as a group outside the Chlorophyta:
later authors have not followed this suggestion.
A newer proposed classification follows Leliaert et al. 2011
and modified with Silar 2016
for the green algae clades and Novíkov & Barabaš-Krasni 2015 for the land plants clade. Notice that the Prasinophyceae are here placed inside the Chlorophyta.
Later, a phylogeny based on genomes and transcriptomes from 1,153 plant species was proposed.
The placing of algal groups is supported by phylogenies based on genomes from the Mesostigmatophyceae and Chlorokybophyceae that have since been sequenced.
The classification of Bryophyta is supported both by Puttick ''et al.'' 2018,
and by phylogenies involving the hornwort genomes that have also since been sequenced.
Embryophytes

The plants that are likely most familiar to us are the
multicellular land plants, called
embryophytes. Embryophytes include the
vascular plants, such as ferns, conifers and flowering plants. They also include the ''
bryophytes'', of which
mosses and
liverworts are the most common.
All of these plants have
eukaryotic cells with
cell walls composed of
cellulose, and most obtain their energy through
photosynthesis, using
light, water and
carbon dioxide to synthesize food. About three hundred plant species do not photosynthesize but are
parasites on other species of photosynthetic plants. Embryophytes are distinguished from
green algae, which represent a mode of photosynthetic life similar to the kind modern plants are believed to have evolved from, by having specialized reproductive organs protected by non-reproductive tissues.
Bryophytes first appeared during the early
Paleozoic. They mainly live in habitats where moisture is available for significant periods, although some species, such as
''Targionia'', are desiccation-tolerant. Most species of bryophytes remain small throughout their life-cycle. This involves an alternation between two generations: a
haploid stage, called the
gametophyte, and a
diploid stage, called the
sporophyte. In bryophytes, the sporophyte is always unbranched and remains nutritionally dependent on its parent gametophyte. The embryophytes have the ability to secrete a
cuticle on their outer surface, a waxy layer that confers resistant to desiccation. In the
mosses and
hornworts a cuticle is usually only produced on the sporophyte.
Stomata are absent from liverworts, but occur on the sporangia of mosses and hornworts, allowing gas exchange.
Vascular plants first appeared during the
Silurian period, and by the
Devonian had diversified and spread into many different terrestrial environments. They developed a number of adaptations that allowed them to spread into increasingly more arid places, notably the vascular tissues
xylem and
phloem, that transport water and food throughout the organism. Root systems capable of obtaining soil water and nutrients also evolved during the Devonian. In modern vascular plants, the sporophyte is typically large, branched, nutritionally independent and long-lived, but there is increasing evidence that Paleozoic gametophytes were just as complex as the sporophytes. The gametophytes of all vascular plant groups evolved to become reduced in size and prominence in the life cycle.
In seed plants, the
microgametophyte is reduced from a multicellular free-living organism to a few cells in a pollen grain and the miniaturised
megagametophyte remains inside the megasporangium, attached to and dependent on the parent plant. A megasporangium enclosed in a protective layer called an integument is known as an
ovule. After fertilisation by means of sperm produced by
pollen grains, an embryo sporophyte develops inside the ovule. The integument becomes a seed coat, and the ovule develops into a seed. Seed plants can survive and reproduce in extremely arid conditions, because they are not dependent on free water for the movement of sperm, or the development of free living gametophytes.
The first seed plants,
pteridosperms (seed ferns), now extinct, appeared in the Devonian and diversified through the Carboniferous. They were the ancestors of modern
gymnosperms, of which four surviving groups are widespread today, particularly the
conifers, which are dominant
trees in several
biomes. The name gymnosperm comes from the
Greek , a composite of ( ) and ( ), as the ovules and subsequent seeds are not enclosed in a protective structure (carpels or fruit), but are borne naked, typically on cone scales.
Fossils

Plant
fossils include roots, wood, leaves, seeds, fruit,
pollen,
spores,
phytoliths, and
amber (the fossilized resin produced by some plants). Fossil land plants are recorded in terrestrial, lacustrine, fluvial and nearshore marine sediments.
Pollen,
spores and algae (
dinoflagellates and
acritarchs) are used for dating sedimentary rock sequences. The remains of fossil plants are not as common as fossil animals, although plant fossils are locally abundant in many regions worldwide.
The earliest fossils clearly assignable to Kingdom Plantae are fossil green algae from the
Cambrian. These fossils resemble
calcified multicellular members of the
Dasycladales. Earlier
Precambrian fossils are known that resemble single-cell green algae, but definitive identity with that group of algae is uncertain.
The earliest fossils attributed to green algae date from the
Precambrian (ca. 1200 mya). The resistant outer walls of
prasinophyte cysts (known as phycomata) are well preserved in fossil deposits of the
Paleozoic (ca. 250–540 mya). A filamentous fossil (''Proterocladus'') from middle Neoproterozoic deposits (ca. 750 mya) has been attributed to the
Cladophorales, while the oldest reliable records of the
Bryopsidales,
Dasycladales) and
stoneworts are from the
Paleozoic.
The oldest known fossils of embryophytes date from the
Ordovician, though such fossils are fragmentary. By the
Silurian, fossils of whole plants are preserved, including the simple vascular plant ''
Cooksonia'' in mid-Silurian and the much larger and more complex
lycophyte ''
Baragwanathia longifolia'' in late Silurian. From the early Devonian
Rhynie chert, detailed fossils of lycophytes and
rhyniophytes have been found that show details of the individual cells within the plant organs and the symbiotic association of these plants with fungi of the order
Glomales. The
Devonian period also saw the evolution of leaves and roots, and the first modern tree, ''
Archaeopteris''. This tree with fern-like foliage and a trunk with conifer-like wood was
heterosporous producing spores of two different sizes, an early step in the evolution of seeds.
The
Coal measures are a major source of
Paleozoic plant fossils, with many groups of plants in existence at this time. The spoil heaps of coal mines are the best places to collect;
coal itself is the remains of fossilised plants, though structural detail of the plant fossils is rarely visible in coal. In the
Fossil Grove at
Victoria Park in
Glasgow, Scotland, the stumps of ''
Lepidodendron'' trees are found in their original growth positions.
The fossilized remains of
conifer and
angiosperm roots,
stems and
branches may be locally abundant in lake and inshore
sedimentary rocks from the
Mesozoic and
Cenozoic eras.
Sequoia and its allies,
magnolia,
oak, and
palms are often found.
Petrified wood is common in some parts of the world, and is most frequently found in arid or desert areas where it is more readily exposed by
erosion. Petrified wood is often heavily
silicified (the
organic material replaced by
silicon dioxide), and the impregnated tissue is often preserved in fine detail. Such specimens may be cut and polished using
lapidary equipment. Fossil forests of petrified wood have been found in all continents.
Fossils of seed ferns such as ''
Glossopteris'' are widely distributed throughout several continents of the
Southern Hemisphere, a fact that gave support to
Alfred Wegener's early ideas regarding
Continental drift theory.
Structure, growth, and development

Most of the solid material in a plant is taken from the atmosphere. Through the process of
photosynthesis, most plants use the energy in
sunlight to convert
carbon dioxide from the atmosphere, plus
water, into simple
sugars. These sugars are then used as building blocks and form the main structural component of the plant.
Chlorophyll, a green-colored,
magnesium-containing
pigment is essential to this process; it is generally present in plant
leaves, and often in other plant parts as well.
Parasitic plants, on the other hand, use the resources of their host to provide the materials needed for metabolism and growth.
Plants usually rely on soil primarily for support and water (in quantitative terms), but they also obtain
compounds of
nitrogen,
phosphorus,
potassium, magnesium and other elemental
nutrients from the soil.
Epiphytic and
lithophytic plants depend on air and nearby debris for nutrients, and
carnivorous plants supplement their nutrient requirements, particularly for nitrogen and phosphorus, with insect prey that they capture. For the majority of plants to grow successfully they also require
oxygen in the atmosphere and around their roots (
soil gas) for
respiration. Plants use oxygen and
glucose (which may be produced from stored
starch) to provide energy. Some plants grow as submerged aquatics, using oxygen dissolved in the surrounding water, and a few specialized vascular plants, such as
mangroves and reed (''
Phragmites australis''),
can grow with their roots in
anoxic conditions.
Factors affecting growth
The genome of a plant controls its growth. For example, selected varieties or genotypes of wheat grow rapidly, maturing within 110 days, whereas others, in the same environmental conditions, grow more slowly and mature within 155 days.
[Robbins, W.W.; Weier, T.E.; ''et al''., ''Botany: Plant Science'', 3rd edition, Wiley International, New York, 1965.]
Growth is also determined by environmental factors, such as
temperature, available
water, available
light,
carbon dioxide and available
nutrients in the soil. Any change in the availability of these external conditions will be reflected in the plant's growth and the timing of its development.
Biotic factors also affect plant growth. Plants can be so crowded that no single individual produces normal growth, causing
etiolation and
chlorosis. Optimal plant growth can be hampered by grazing animals, suboptimal soil composition, lack of
mycorrhizal fungi, and attacks by insects or
plant diseases, including those caused by bacteria, fungi, viruses, and nematodes.

Simple plants like algae may have short life spans as individuals, but their populations are commonly seasonal.
Annual plants grow and reproduce within one
growing season,
biennial plants grow for two growing seasons and usually reproduce in second year, and
perennial plants live for many growing seasons and once mature will often reproduce annually. These designations often depend on climate and other environmental factors. Plants that are annual in
alpine or
temperate regions can be biennial or perennial in warmer climates. Among the vascular plants, perennials include both
evergreens that keep their leaves the entire year, and
deciduous plants that lose their leaves for some part of it. In temperate and
boreal climates, they generally lose their leaves during the winter; many
tropical plants lose their leaves during the
dry season.
The growth rate of plants is extremely variable. Some mosses grow less than 0.001 millimeters per hour (mm/h), while most trees grow 0.025–0.250 mm/h. Some climbing species, such as
kudzu, which do not need to produce thick supportive tissue, may grow up to 12.5 mm/h.
Plants protect themselves from
frost and
dehydration stress with
antifreeze proteins,
heat-shock proteins and sugars (
sucrose is common). LEA (
Late Embryogenesis Abundant) protein expression is induced by stresses and protects other proteins from aggregation as a result of
desiccation and
freezing.
Effects of freezing
When water freezes in plants, the consequences for the plant depend very much on whether the freezing occurs within cells (intracellularly) or outside cells in intercellular spaces.
[Glerum, C. 1985. Frost hardiness of coniferous seedlings: principles and applications. pp. 107–123 ''in ''Duryea, M.L. (Ed.). Proceedings: Evaluating seedling quality: principles, procedures, and predictive abilities of major tests. Workshop, October 1984, Oregon State Univ., For. Res. Lab., Corvallis OR.] Intracellular freezing, which usually kills the cell
[Lyons, J.M.; Raison, J.K.; Steponkus, P.L. 1979. The plant membrane in response to low temperature: an overview. pp. 1–24 ''in'' Lyons, J.M.; Graham, D.; Raison, J.K. (Eds.). Low Temperature Stress in Crop Plants. Academic Press, New York NY.] regardless of the hardiness of the plant and its tissues, seldom occurs in nature because rates of cooling are rarely high enough to support it. Rates of cooling of several degrees Celsius per minute are typically needed to cause intracellular formation of ice.
[Mazur, P. 1977. The role of intracellular freezing in the death of cells cooled at supraoptimal rates. Cryobiology 14:251–272.] At rates of cooling of a few degrees Celsius per hour, segregation of ice occurs in intercellular spaces.
[Sakai, A.; Larcher, W. (Eds.) 1987. Frost Survival of Plants. Springer-Verlag, New York. 321 p.] This may or may not be lethal, depending on the hardiness of the tissue. At freezing temperatures, water in the intercellular spaces of plant tissue freezes first, though the water may remain unfrozen until temperatures drop below .
After the initial formation of intercellular ice, the cells shrink as water is lost to the segregated ice, and the cells undergo freeze-drying. This dehydration is now considered the fundamental cause of freezing injury.
DNA damage and repair
Plants are continuously exposed to a range of biotic and abiotic stresses. These stresses often cause
DNA damage directly, or indirectly via the generation of
reactive oxygen species.
Plants are capable of a DNA damage response that is a critical mechanism for maintaining genome stability.
The DNA damage response is particularly important during
seed germination, since seed quality tends to deteriorate with age in association with DNA damage accumulation.
During germination repair processes are activated to deal with this accumulated DNA damage.
In particular, single- and double-strand breaks in DNA can be
repaired.
The DNA checkpoint kinase
ATM has a key role in integrating progression through germination with repair responses to the DNA damages accumulated by the aged seed.
Plant cells

Plant cells are typically distinguished by their large water-filled central
vacuole,
chloroplasts, and rigid
cell walls that are made up of
cellulose,
hemicellulose, and
pectin.
Cell division is also characterized by the development of a
phragmoplast for the construction of a
cell plate in the late stages of
cytokinesis. Just as in animals, plant cells differentiate and develop into multiple cell types.
Totipotent meristematic cells can differentiate into
vascular, storage, protective (e.g.
epidermal layer), or
reproductive tissues, with more primitive plants lacking some tissue types.
Physiology
Photosynthesis
Plants are
photosynthetic, which means that they manufacture their own food molecules using energy obtained from
light. The primary mechanism plants have for capturing light energy is the
pigment chlorophyll. All green plants contain two forms of chlorophyll,
chlorophyll ''a'' and
chlorophyll ''b''. The latter of these pigments is not found in red or brown algae.
The simple equation of photosynthesis is as follows:
:
6CO2 + 6H2O ->textC6H12O6 + 6O2
Immune system
By means of cells that behave like nerves, plants receive and distribute within their systems information about incident light intensity and quality. Incident light that stimulates a chemical reaction in one leaf, will cause a chain reaction of signals to the entire plant via a type of cell termed a ''bundle sheath cell''. Researchers, from the
Warsaw University of Life Sciences in Poland, found that plants have a specific memory for varying light conditions, which prepares their immune systems against seasonal pathogens. Plants use pattern-recognition receptors to recognize conserved microbial signatures. This recognition triggers an immune response. The first plant receptors of conserved microbial signatures were identified in rice (XA21, 1995) and in ''
Arabidopsis thaliana'' (FLS2, 2000). Plants also carry immune receptors that recognize highly variable pathogen effectors. These include the NBS-LRR class of proteins.
Internal distribution
Vascular plants differ from other plants in that nutrients are transported between their different parts through specialized structures, called
xylem and
phloem. They also have
roots for taking up water and minerals. The xylem moves water and minerals from the root to the rest of the plant, and the phloem provides the roots with sugars and other nutrient produced by the leaves.
Genomics
Plants have some of the largest
genomes among all organisms. The largest plant genome (in terms of gene number) is that of
wheat (''Triticum asestivum''), predicted to encode ≈94,000 genes and thus almost 5 times as many as the
human genome. The first plant genome sequenced was that of ''
Arabidopsis thaliana'' which encodes about 25,500 genes. In terms of sheer DNA sequence, the smallest published genome is that of the carnivorous
bladderwort (''Utricularia gibba)'' at 82 Mb (although it still encodes 28,500 genes) while the largest, from the
Norway Spruce (''Picea abies''), extends over 19,600 Mb (encoding about 28,300 genes).
Ecology
The photosynthesis conducted by land plants and algae is the ultimate source of energy and organic material in nearly all ecosystems. Photosynthesis, at first by cyanobacteria and later by photosynthetic eukaryotes, radically changed the composition of the early Earth's anoxic atmosphere, which as a result is now 21%
oxygen. Animals and most other organisms are
aerobic, relying on oxygen; those that do not are confined to relatively rare
anaerobic environments. Plants are the
primary producers in most terrestrial ecosystems and form the basis of the
food web in those ecosystems. Many animals rely on plants for shelter as well as oxygen and food. Plants form about 80% of the world
biomass at about of carbon.
Land plants are key components of the
water cycle and several other
biogeochemical cycles. Some plants have
coevolved with
nitrogen fixing bacteria, making plants an important part of the
nitrogen cycle. Plant roots play an essential role in
soil development and the prevention of
soil erosion.
Distribution
Plants are distributed almost worldwide. While they inhabit a multitude of
biomes and
ecoregions, few can be found beyond the
tundras at the northernmost regions of
continental shelves. At the southern extremes, plants of the
Antarctic flora have adapted tenaciously to the prevailing conditions.
Plants are often the dominant physical and structural component of habitats where they occur. Many of the Earth's
biomes are named for the type of vegetation because plants are the dominant organisms in those biomes, such as
grasslands,
taiga and
tropical rainforest.
Ecological relationships

Numerous animals have coevolved with plants. Many animals
pollinate flowers in exchange for food in the form of pollen or
nectar. Many animals
disperse seeds, often by eating
fruit and passing the seeds in their
feces.
Myrmecophytes are plants that have coevolved with
ants. The plant provides a home, and sometimes food, for the ants. In exchange, the ants defend the plant from
herbivores and sometimes competing plants. Ant wastes provide organic
fertilizer.
The majority of plant species have various kinds of fungi associated with their root systems in a kind of
mutualistic symbiosis known as
mycorrhiza. The fungi help the plants gain water and mineral nutrients from the soil, while the plant gives the fungi carbohydrates manufactured in photosynthesis. Some plants serve as homes for
endophytic fungi that protect the plant from herbivores by producing toxins. The fungal endophyte, ''
Neotyphodium coenophialum'', in
tall fescue (''Festuca arundinacea'') does tremendous economic damage to the cattle industry in the U.S.
Various forms of parasitism are also fairly common among plants, from the semi-parasitic
mistletoe that merely takes some nutrients from its host, but still has photosynthetic leaves, to the fully parasitic
broomrape and
toothwort that acquire all their nutrients through connections to the roots of other plants, and so have no
chlorophyll. Some plants, known as
myco-heterotrophs, parasitize mycorrhizal fungi, and hence act as
epiparasites on other plants.
Many plants are
epiphytes, meaning they grow on other plants, usually trees, without parasitizing them. Epiphytes may indirectly harm their host plant by intercepting mineral nutrients and light that the host would otherwise receive. The weight of large numbers of epiphytes may break tree limbs.
Hemiepiphytes like the
strangler fig begin as epiphytes but eventually set their own roots and overpower and kill their host. Many
orchids,
bromeliads,
ferns and
mosses often grow as epiphytes. Bromeliad epiphytes accumulate water in leaf axils to form
phytotelmata that may contain complex aquatic food webs.
Approximately 630 plants are
carnivorous, such as the
Venus Flytrap (''Dionaea muscipula'') and
sundew (''Drosera'' species). They trap small animals and digest them to obtain mineral nutrients, especially
nitrogen and
phosphorus.
[Barthlott, W.; Porembski, S.; Seine, R.; Theisen, I. 2007. ''The Curious World of Carnivorous Plants: A Comprehensive Guide to Their Biology and Cultivation.'' Timber Press: Portland, Oregon.]
Competition
Competition occurs when members of the same species, or several different species, compete for shared resources in a given habitat. According to the competitive exclusion principle, when environmental resources are limited, species cannot occupy nor be supported by identical niches.
Eventually, one species will out-compete the other, which will push the disadvantaged species to extinction.
In regard to plants, competition tends to negatively affect their growth when competing for shared resources.
These shared resources commonly include space for growth, sunlight, water and nutrients. Light is an important resource because it is necessary for photosynthesis.
Plants use their leaves to shade other plants from sunlight and grow quickly to maximize their own expose.
Water is also important for photosynthesis, and plants have different root systems to maximize water uptake from soil.
Some plants have deep roots that are able to locate water stored deep underground, and others have shallower roots that are capable of extending longer distances to collect recent rainwater.
Minerals are also important for plant growth and development, where deficiencies can occur if nutrient needs are not met. Common nutrients competed for amongst plants include nitrogen and phosphorus. Space is also extremely important for a growing and developing plant.
Having optimal space makes it more likely that leaves are exposed to sufficient amounts of sunlight and are not overcrowded in order for photosynthesis to occur.
In the event that an old tree dies, competition arises amongst a number of trees to replace it.
Those that are less effective competitors are less likely to contribute to the next generation of offspring.
Importance
Cultivation
The study of plant uses by people is called economic botany or
ethnobotany. Human cultivation of plants is part of
agriculture, which is the basis of human civilization. Plant agriculture is subdivided into
agronomy,
horticulture and
forestry.
Food

Humans depend on plants for
food, either directly or as feed for
domestic animals.
Agriculture deals with the production of food crops, and has
played a key role in the history of world civilizations. Agriculture includes
agronomy for arable crops,
horticulture for vegetables and fruit, and
forestry for timber.
About 7,000 species of plant have been used for food, though most of today's food is derived from only 30 species. The major
staples include
cereals such as
rice and
wheat, starchy roots and tubers such as
cassava and
potato, and
legumes such as
peas and
beans.
Vegetable oils such as
olive oil provide
lipids, while
fruit and
vegetables contribute
vitamins and minerals to the diet.
Medicines
Medicinal plants are a primary source of
organic compounds, both for their medicinal and physiological effects, and for the industrial
synthesis of a vast array of organic chemicals. Many hundreds of medicines are derived from plants, both traditional medicines used in
herbalism and chemical substances purified from plants or first identified in them, sometimes by
ethnobotanical search, and then
synthesised for use in modern medicine. Modern medicines derived from plants include
aspirin,
taxol,
morphine,
quinine,
reserpine,
colchicine,
digitalis and
vincristine.
Plants used in herbalism include
ginkgo,
echinacea,
feverfew, and
Saint John's wort. The
pharmacopoeia of
Dioscorides, ''
De Materia Medica'', describing some 600 medicinal plants, was written between 50 and 70 AD and remained in use in Europe and the Middle East until around 1600 AD; it was the precursor of all modern pharmacopoeias.
Nonfood products

Plants grown as industrial crops are the source of a wide range of products used in manufacturing, sometimes so intensively as to risk harm to the environment. Nonfood products include
essential oils,
natural dyes, pigments, waxes,
resins,
tannins, alkaloids, amber and
cork. Products derived from plants include soaps, shampoos, perfumes, cosmetics, paint, varnish, turpentine, rubber,
latex, lubricants, linoleum, plastics, inks, and
gums. Renewable fuels from plants include
firewood,
peat and other
biofuels.
The
fossil fuels
coal,
petroleum and
natural gas are derived from the remains of aquatic organisms including
phytoplankton in
geological time.
Structural resources and fibres from plants are used to construct dwellings and to manufacture clothing.
Wood is used not only for buildings, boats, and furniture, but also for smaller items such as
musical instruments and sports equipment. Wood is
pulped to make paper and cardboard. Cloth is often made from
cotton,
flax,
ramie or synthetic fibres such as
rayon and
acetate derived from plant
cellulose.
Thread used to sew cloth likewise comes in large part from cotton.
Aesthetic uses

Thousands of plant species are cultivated for aesthetic purposes as well as to provide shade, modify temperatures, reduce wind, abate noise, provide privacy, and prevent soil erosion. Plants are the basis of a multibillion-dollar per year tourism industry, which includes travel to
historic gardens,
national parks,
rainforests,
forests with colorful autumn leaves, and festivals such as
Japan's and
America's cherry blossom festivals.
While some
gardens are planted with food crops, many are planted for aesthetic, ornamental, or conservation purposes.
Arboretums and
botanical gardens are public collections of living plants. In private outdoor gardens, lawn grasses, shade trees, ornamental trees, shrubs, vines, herbaceous perennials and bedding plants are used. Gardens may cultivate the plants in a naturalistic state, or may sculpture their growth, as with
topiary or
espalier.
Gardening is the most popular leisure activity in the U.S., and working with plants or
horticulture therapy is beneficial for rehabilitating people with disabilities.
Plants may also be grown or kept indoors as
houseplants, or in specialized buildings such as
greenhouses that are designed for the care and cultivation of living plants.
Venus Flytrap,
sensitive plant and
resurrection plant are examples of plants sold as novelties. There are also art forms specializing in the arrangement of cut or living plant, such as
bonsai,
ikebana, and the arrangement of cut or dried flowers.
Ornamental plants have sometimes changed the course of history, as in
tulipomania.
Architectural designs resembling plants appear in the capitals of
Ancient Egyptian columns, which were carved to resemble either the
Egyptian white lotus or the
papyrus. Images of plants are often used in painting and photography, as well as on textiles, money, stamps, flags and coats of arms.
Scientific and cultural uses
Basic biological research has often been done with plants. In
genetics, the breeding of pea plants allowed
Gregor Mendel to derive the basic laws governing inheritance, and examination of
chromosomes in maize allowed
Barbara McClintock to demonstrate their connection to inherited traits. The plant ''
Arabidopsis thaliana'' is used in laboratories as a
model organism to understand how
genes control the growth and development of plant structures.
NASA predicts that space stations or space colonies will one day rely on plants for
life support.
Ancient trees are revered and many are
famous.
Tree rings themselves are an important method of dating in archeology, and serve as a record of past climates.
Plants figure prominently in
mythology, religion and
literature. They are used as
national and state emblems, including
state trees and
state flowers. Plants are often used as memorials, gifts and to mark special occasions such as births, deaths, weddings and holidays. The arrangement of flowers may be used to send hidden
messages.
Negative effects
Weeds are unwanted plants growing in managed environments such as
farms,
urban areas,
gardens,
lawns, and
parks. People have spread plants beyond their native ranges and some of these introduced plants become
invasive, damaging existing ecosystems by displacing native species, and sometimes becoming serious weeds of cultivation.
Plants may cause harm to animals, including people. Plants that produce
windblown pollen invoke allergic reactions in people who suffer from
hay fever. A wide variety of plants are
poisonous.
Toxalbumins are plant poisons fatal to most mammals and act as a serious deterrent to consumption. Several plants cause skin irritations when touched, such as
poison ivy. Certain plants contain
psychotropic chemicals, which are extracted and ingested or smoked, including
nicotine from
tobacco,
cannabinoids from
Cannabis sativa,
cocaine from
Erythroxylon coca and
opium from
opium poppy.
Smoking causes damage to health or even death, while some drugs may also be harmful or fatal to people. Both illegal and legal drugs derived from plants may have negative effects on the economy, affecting worker productivity and law enforcement costs.
See also
*
Biosphere
*
Evolutionary history of plants
*
Plant defense against herbivory
*
Plant identification
*
Plant reproduction
*
Plant to plant communication via mycorrhizal networks
*
The Plant List
*
References
Further reading
;General:
* Evans, L.T. (1998). ''Feeding the Ten Billion – Plants and
Population Growth''.
Cambridge University Press. Paperback, 247 pages. .
* Kenrick, Paul & Crane, Peter R. (1997). ''The Origin and Early Diversification of Land Plants: A Cladistic Study''. Washington, D.C.: Smithsonian Institution Press. .
* Raven, Peter H.; Evert, Ray F.; & Eichhorn, Susan E. (2005). ''Biology of Plants'' (7th ed.). New York: W.H. Freeman and Company. .
* Taylor, Thomas N. & Taylor, Edith L. (1993). ''The Biology and Evolution of Fossil Plants''. Englewood Cliffs, NJ: Prentice Hall. .
*
;Species estimates and counts:
* International Union for Conservation of Nature and Natural Resources (IUCN) Species Survival Commission (2004).
IUCN Red Listbr>
*
External links
* (requires
Microsoft Silverlight)
*
Index Nominum AlgarumPlant Resources of Tropical AfricaTree of Life
;Botanical and vegetation databases
African Plants Initiative databaseAustraliaChilean plants at ''Chilebosque''e-Floras (Flora of China, Flora of North America and others)Flora of Central Europe
Flora of North AmericaMeet the Plants-National Tropical Botanical GardenLady Bird Johnson Wildflower Center – Native Plant Information Network at University of Texas, AustinThe Plant ListUnited States Department of Agriculturenot limited to continental US species
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Plants