Orchid

Orchidaceae
Cypripedium reginae
Scientific classification
Domain: Eukaryota Kingdom: Plantae Division: Magnoliophyta Class: Liliopsida Order: Asparagales Family: Orchidaceae Juss. 1789
Type genus
Orchis L. 1753
Subfamilies
Apostasioideae Garay 1960 Vanilloideae Szlach. 1995 Cypripedioideae Garay 1960 Orchidoideae Eaton 1836 Epidendroideae Lindl. 1821
Synonyms
Apostasiaceae Lindl. 1833 Cypripediaceae Lindl. 1833 Limodoraceae Horan. 1847 Neottiaceae Horan. 1834 Vanillaceae Lindl. 1835 Neuwiediaceae (Burns-Balogh & Funk) R.Dahlgren ex Reveal & Hoogland 1991

There are literally tens of thousands of species, cultivars and varieties in the orchid family, the largest family of flowering plants. The word orchid may refer to any of the botanical family Orchidaceae, or, more commonly among lay persons, any of thousands of flowers called "orchids".

Orchids are ancient, and have been cultivated for centuries. They range from rare and recent discoveries such as the tiny Tallong Midge Orchid to the large, showy orchids which are featured in bouquets and corsages, to food orchids such as Vanilla. A few orchids have insignificant flowers and are grown for their foliage.

Because orchids are generally epiphyte plants, the material available for their nourishment is scarse and the water is available only from the rain and humidity from the air, therefore orchids learnt how to maximize the utilization of the few available resources. They adapted to keep water in ther thickened, almost succulent stems, called pseudobulbs, or in highly porous roots recovered by a spongy layer called vellamen, capable of absorbing humidity from the air; or in thick leaves; and yet, when terrestrial, in small root tubercules. For the same reason, they are plants that go through long periods of rest when their metabolism is reduced, followed by a fast growth, blooming during the time of the year when the resources are more abundant or imediately thereafter. Many species loose their leaves to avoid dehydration during the droughs or while they are resting.

Orchids seemed to be fascinating: every developed nation has many orchid societies, and this fascination extends beyond form and beauty. Because of their biological importance (some orchids have developed extraordinary systems of pollination, for example, "Lady's Slipper" traps insects and so forces them to pollinate the flower; one Australian orchid exists underground and is pollinated by ants; many give off attractive odours), orchids hold just as much interest for scientists. Famed biologist Ernst Mayr discovered and named 38 new species of orchid.

Distribution

Despite their distribution is largely irregular throughout the globe, orchids can be found in almost all regions of the planet, except Antartic continet. Due to their wide greographic distribution, it is natural that a so diverse group of plants show high degree of adaptation to different climates and to the multiplicity of polinators present in each area. The number of orchid genera that exist on every continent is not exact because there is no consensus among the taxonomists about how to split them, however, it can be estimated as follow: Eurasia, about 50 genera; North America, circa 25 genera, Latin America and Caribbean, between 300 and 350; tropical Asia, between 250 and 300; tropical Africa, circa 250; and Oceania, about 60.

The largest diversity of orchid species occurs in tropical areas of the globe, notably on mountain areas, which are natural bareers that insolate the several populations of plants. Islands also favor development of species but unlikely mountain areas, islands do not favor diversity that much because, unless the island is large enough to have a variety of climates, what is more commen is to find a high number of few endemic species that do not exist anywhere else. Exceptions are large islands as Borneo, New Guinea, Madagascar and some other, where the diversity is enormous, these have both a high number of endemisms and wealthy of different species. Therefore, some of the main areas in the world noted for having a large number of species are the Islands os Southeast Asia, the mountain areas of Ecuador and Colombia and the Atlantic Jungle along Brazilian coastal mountains, where there are more than fifteen hundred species. Other important diversity areas are the mountains of Mesoamerica and the ones south of Himalaya, in India and China, besides the southeast of Africa, particularly Madagascar. Ecuador is the country where the largest number of orchid species is reported, up to 3,549, imediately followed by Colombia, with 2,723, New Guinea, 2,717, and Brazil, with a total of 2,590. Among others, Borneo, Sumatra, Madagascar, Venezuela and Costa Rica, are countries with high number of species.

Habit

Orchids adapted to the most different environments. They may be terrestrial, growing on grassfields and savannahs among the grass, or on the soil of shady forests, epiphytic over trees or bushes, close to the soil sheltered from bright sunlight, or clore to the top of the trees and cacti, exposed to strong sunlight; they may be lithophyte growing over rocky soil or directly on the stones, they may be psamophytics oalong the sand of the beaches,saprophytic on decaying material over the soil or rarely acquatical, or paludicolous, in marshes and swamp areas. There is also an extreem case of a subterraneous species from Australia whose only the flowers occasionally emerge straight from the soil.

The most common kinds of orchids in each of these areas are highly variable. On tropical regions, where the light and humidity are high, yet the competition for light with tree species is strong, the orchids tent to be predominat epiphytical, however, many species of terrestrial species, able to thrive without high amounts of light do exist too. Looking for light, under the shadow of trees up to forty meters tall, this herbs grow over their branches and stems, at diverse heights, according to the necessities of each species. Their roots, exposed to the air, obtain most ot the nutrients from decaying material that acumulates around them, from the rains that washes the tree leaves from above, or from the air dust. Orchid roots are recovered by a spongy tissue called velamen. Associated with the velamen, most of orchids host a fungus known as Mycorrhyza that helps on decomposing of organic material breaking them into mineral salts, making easier their absortion by orchids. In extreem conditions, orchids may to some extent, absorve water and nutrients thorough the pores on their leaves, leaving to the roots only the function of sustaining the plant attached to the substract. No orchid is a parasite, what means their presence never damages their hosts, despite, in exceptional cases, some tree branches may not be strong enough to sustain the weight of a large colony and may end broken. There are many terrestrial orchids on tropical areas too, although, differently form the ones from temperate regions, many may keep growing almost constantly during most of the year. The great amount of organic material available on forests soil favors the occurence of few saprophytic species of orchids without chlorophyll, which obtain all their nutrients from substances rejected by the processing of decomposing material by fungi associated to them.

In regions where the climate is colder, where the grassfilds are most common, or in dryer and rockier areas with small bushes, orchids are basicly terrestrial plants with buried roots, sometimes developes into tubercules which eneble them to resist winter and snow, ot to long droughs and occasional fires. The snow might frost epiphytic species withouth sheltered roots to store the nutrients needed to shot a new grouth in springtime. Also the fires would enterely burn epiphyitic species. In this areas subject to most defined seasonal climatel, the plants normally hace a distinct period of dormancy while often their aerial segments die to avoid damages to their physiology due to extreem droughs or cold.

Some especies are considered endangered of extinction in the wild, both because of extensive collection, as due to the cut of forests for agriculture and even by the utilization of defoliating substances during wars from the past. Surpringly enough, the majority of the endangered species are included among the most common under cultivation and the more frequently commercially grown. Most of really rare species are not found on the lists of endangered species because they have no comercial value and low interest because of their tiny flowers or difficulty of culture. Ordinarily, for the same reasons, governments do not sponsor any surveys about the existing population of these in the wild and the few ones that exist are just occasional or made by private or academic researchers.

Other important fact to consider against extinction is that each orchid fruit can contain hundreds of thousands seeds, and that the existence of two or three individuals unter culture may produce, in a few years, a fantastic number of plants, making the extinction threat of an orchid much different from the same threat to an animal, that just have one or few cubs each pregnancy.

Taxonomy

Orchidaceae is considered one of the largest, if not the largest, family among all plant families. The number of species is close to 25 thousand, corresponding to about eight percent of all seed plants. The exact number of accepted species is four times bigger than the mammal species and two times the birds. These impressive numbers do not take into account the huge amount of new hybrids and varieties produced by orchid growers every year. Moroever, even today, hundreds of new species are described yearly, both because of revisions of long established genera but whose species were not well determinated, as due to new species discovered in nature. Only in 2008 the International Plant Names Index registrered more than four hundred new descriptions.

The orchid family was established when Antoine Laurent de Jussieu published his Genera Plantarum, in 1789. However, before Jussieu's classification, Linnaeus already had described eight orchid genera which, nevertheless, did not form a family. At the time all epiphytic species belonged to the genus Epidendrum. Other genus described by Linnaeus was Orchis, a greek word refering to the shape of two small tubercules that the species of this genus show, which resemble testicles. As this was the first orchid genus to be formally described, from it derived the name of the whole family.

Since Orchidaceae was proposed, the research on its species has not been interrupted. Their classification passed through numberless revisions and the amount of known genera they are divided has been increasing throughout the years, now reaching more than eight hundred. Their exact number is not known because there is no consensus about the best way of splitting the genera. According to each reference, the list of accepted genera are diverse and the total number much different. A good example is a comparation between the number of genera published since 2002 to classify species before subordinated to genus Dendrobium, about thirty, and the number of these which are actually accepted by the database of the Royal Botanic Garden, three or four. The most recent trend is the classification based upon genetic, or molecular information called Phylogeny, which in theory reflects the evolutionary relations among each one of the species, groups of species, genera, and so forth. However, this system is comparatively new and not all researchers fully accept it, many still basing their conclusions mostly on morphologycal diagnosis. The debate is lively held on both fronts. One of the defensors of Phylogenetics is Mark Chase, who places morphology on a secondary level, Among the morphologists one of the most noted is Carlyle August Luer, who since 1978 dedicated to study the species of subtribe Pleurothallidinae and thinks atha phylogenetic should be regarded only as an extra tool for now. Luer has described about three thousand new species of orchids.

Orchidaceae is a family passing through an active cycle of evoluctionary development. Traditionaly, Biology considers the species concept as a group of beings that can breed producing fertile descendants. Orchid species are slightly different because they do not fit well in this concept. Not only most of the species can interbreed with several other producing fertile descendants, as most of the genera that belong to the same subtribe can do too. It is not uncommon to encounter natural hybrids between diferent species and genera in the wild, and although almost all these plants are fertile, the are not more common just because as orchids are highly adaptated to their polinator, these hybrids may occur by chance and their particular resulting morphology are not really adaptated to the existing polinators. There are some rare exceptions, when these hybrids are result of breedings of two closely related species and still can be polinated by the same polinators of parent species. When this happens it is more likely that along the years a new species can appear. This may be the case of Cattleya × mesquitae. It is a natural hybrid discovered in 1996 in Goiás State in Brazil. We know know that this species is a result of a high degree of interbreeding of Cattleya walkeriana and Cattleya nobilior. As the result of this breeding is pollinated by the same agents of its parents, the crossing has been occuring again and again between the three species from the area along the ages, thus one of the original parents cannot be found there anymore. All original plants have crossed and faded. Today we know Cattleya × mesquitae is a hybrid because similar plants have been procuced by artificial breedings. Lou Menezes, its describer, claims that this species is so ancient that they have even evolved in nature, developing a fragrance that is not present on the hybrids artificially produced. This is one of the ways a new species can appear in the wild. Cases like this are not uncommon among orchids, therefore many species are hard to circunscribe exactly because they result of different degrees of breedings between closely related species in a given area. Furthermore orchid hybrids produce variable descendents that may be closer to either one of the parents or an intermediate mixture of both. It is also possible that one day many species described by Botanists may be proved to be in fact natural hybrids long stablished in nature.

The circunscription of each species sometimes is complicated even further because many groups may be isolated and show subtle differences that some taxonomists may think are enough to establish independent species while other may think these are just natural variations of populations separated for long time but not yet important enough to justify the stablisment of another species. Therefore the exact number of orchid species to be accepted by the scientific comunity is highly variable according to each reference. Today many taxonomists would rather classity these groups of species as superspecies or complexes of cryptic species. In these cases the differences between the extreem variations of a grrop con be clearly seen, but there are so many intermediate forms that placing exact limits between several species is almost impossible. There are many examples of these groups, as such the ones of Brasiliorchis picta, Anacheilium vespa, Heterotaxis crassifolia, and countless others.

The orchid family is formed by five subfamilies:

• Apostasioideae Reichenbach

Plants with mealy or paste-like pollen, which ordinaily are not agregated into pellets, called pollinia, with two or three fertile long anthers, leaves with stealthing bases, elongated staminodium and labellum similar to the petals. It is the smallest subfamily, not split into tribes but only two genera and sixteen species from southeast Asia;

• Cypripedioideae Lindley

Plants with mealy or paste-like pollen, which ordinaily are not agregated into pollinia, with two oblong or oval anthers, leaves with stealthing bases, shelter-like staminodium and labellum generally saccate. This sbubfamily is split in five genera and 170 species spread though the world temperate areas, few encountered in tropical America;

• Vanilloideae Szlachetko

Plants with mealy or paste-like pollen, which ordinaily are not agregated into pollinia, with one fertile incumbent anther only and leaves withouth stealthing bases. It is divided into two tribes, fifteen genera and 250 species spread throughout the humid tropical and subtropical areas of the world, and east of United States of America;

• Orchidoideae Lindley

Plants with coherent pollen forming pollinia, with one fertile anther, erect or bent back, and convolute leaves but not very plicate, roots ordinarily fleshy or tuberouus. This subfamily is formed by six tribes and several subtribes, encompassing 208 genera and 3630 species distributed along almost all over the world, except the dryer deserts and polar areas;

• Epidendroideae Lindley

Plants with coherent pollen forming pollinia and with one incumbent anther only, or with the anther bent back, but then with clearly plicate leaves and roots hardly ever fleshy. This is the largest subfamily, formed by several tribes and subtribes, more than five hundred genera and about twinty thousand species, distributed along the same areas of Orchidoideae, despite there are also subterrain species living at the deserts of Australia.

The division of the orchid species by genera is highly irregular. There is a great number of genera with one species only and some huge genera bearing more than a thousand. Despite many or these large genera are going through revision and breaking into smaller and handier genera many are not. We mention some of there larger genera as they were classified at the end of 2007: Bulbophyllum with alomost two thousand species; Lepanthes, Stelis, Epidendrum, Pleurothallis, and Dendrobium with more than a thousand; Oncidium, Habenaria and Maxillaria bearing circa seven hundred; and Masdevallia, with more than five hundred.

Morphology

Among all the characteristics that distinguish Orchidaceae, very few are shared by all its species. This happens because orchids are a recent family in active evolution. Some groups of orchids derived from the core group of original ancestors very early, possibly during their first evolutionary steps, and have reatained many of their qualities, while others remained constant and derived much later. As the orchids have shown an enormous capacity of adaptation, this has led to an equaly huge number of variations and species.

The most important characteristics shared by orchids are:

• The presence of the column, a structure orginated from the fusion of the flowers male and female sexual organs;
• Pollen frequently aggregated into cartilaginous structures called pollinia;
• very small seeds, almost without nutrients, formed by few cells, whigh only germinate when certain fungi are present;
• Flowers of lateral simmetry, not radial, composed by six segments, three external ones called sepals, and tree internal, called petals. From de later, one is different, called labellum, which normally ir responsible for pollinators atraction to the column, and participates actively of pollination mechanism.
• Orchid flowers usually are presented inverted from the natural position due to a proccess known as ressupination, when during the bud growth, the ovarium twists itself 180º;
• Most of epiphytic species has their roots recovered by a spongy tissue called vellamen;
• The life sapn of an orchid is undeterminated becaus the grow indefinitely, continuously or during short anual periods, in theory for unlimited time. Few is known about the age an orchid can reach but there are records of their longevity both from the oldest specimen under culture at the Royal Botanic Garden, which is orlder than two hundred years, as for a plant that belongs to the Círculo Americanense de Orquidófilos, already cultivated for more than one hundred years.

For all named characteristics there are abundant exceptions, however, all orchids share, at different degrees, several of them.

Growth

Orchids growth occurs in several diverent patterns, it may be continuous or seazonal, sympodial or monopodial, grouped ou spaced, ascendent or pendent, aerial or buried. Depending upon the environment condition, certain growth forms are predominant. On tropical areas cuntinuous growth is more common, despite there are also a high number of species of seazonal growth. In areas subjecto to droughs or intense cold, the seazonal growth is the rule. Monopodial orchids ususally grow continuously, sympodial, ordinarily show certain seazonality.

Roots

Orchids have no primary roots, that are main central roots where secondary roots grow from, but only the secondary roots, which start directly from the stem and, ocasionally, from other secondary roots. Frequently the roots act as a storage of nutrients and water, helping the plant to retain and acumulate nutritional substances that deposit on their bases. In some cases the roots are chlorophyllated organs capable of carrying photosyntheses during the periods when the plants loose their leaves. Their roots show varied thicknesses, from highly thin to extremelly thick. Roots structure is highly variable among orchid genera, according to the way and the places they grow.

The epiphytic species generally present robust roots, cylindrical when aerial, which become flatter after attached to the substract. They are frequently recovered by the vellamen, which is a thick spongy tissue that is very important to enable orchids to quickly absorb high quantities of water from the rains and even humidity from the air.

The terrestrial species normaly bear some roots thickened into small or large strucures that resenble tubercules, which may be spherical to elongated cylinders which act as storage of water and nutrients, replacing the role carried by the pseudobulbs usually present on epiphytic species. Occasionally these tubercules split from the mother plant originating new plants.

The roots life time varies according to environmental conditions and generally is inferior to the stem life time. New roots usually shot during or at the end of each plant vegetative growth period. Despite this is not the primary nutritional source of orchids, they usually benefit from a kind of symbiosis or association with a fungus called Micorrhyza lodged on the vellamen exterior cells of their roots and excretes several nitrients directly absorbed their roots.

Stems

On epiphytic species of sympodial growth the stem usually is formed by two segments, one of them, called rhyzome, shows reptant growth, which means it grows along the substract, and can be short or elongated, thin or thick; the other segment is aerial and may or may not be thickened into a structure called pseudobulb, which acts as water and nutrients storage. In some epiphytic genera, particularly the ones related to genus Huntleya, the secondary, or aerial stem, is reduced to an inconspicuous node which originates the leaves. Sympodial orchids usually show seazonal growth and new secondary stems are added each period.

On epiphytic species of monopodial growth the stem is formed by the aerial segment only. It may be erect or pendent and its extremity growns continuously forming new leaves and ocasional lateral roots or new growths along the stem. The stem of this kind of orchids is never thickened into pseudobulbs, however their leaves and roots ordinarily are comparatively thicker than the epiphytic ones, as they frequently help retaining water and nutrients.

Terrestrial species may or may not have developed stems and these, different from epiphytic orchids which always show perenial stems, may be partially or enterely deciduous. Some terrestrial orchids present very long stems, which sometimes reach more than six meters of length.

Leaves

The majority of orchids have leaves of longitudinal parallel venation with hardly visible crossings. Usually arranged in tow alternated opposed rows, both sides of the stem. Many species have only one pseudo-terminal leave and an aborted growth. Their shape, thickness, quantity, color, size and the way they grow is highly variable.

• The shape of their blades can be circular, elliptical, lanceolated, oval, linear, oblong, spatulated, besides endless intermediate forms.
• The leaves apex may be rounded, acuminated, acute, thin or thick, pointed, radial, or uneven.
• Their edges are ordinarily smooth, partialy curved, hardly ever denticulated.
• Their structure may or may not show a petiole, with a variable number of longitudinal paralell nerves, very visible or almost imperceptible.
• The thicknes goes from very thing and maleable or fleshy, firm and breakable to enterely succulent.
• Ordinarily bearing the most diverse shades of green, their colors may also be completely diferent according to the faces, from red to dark brown, grey tones, blueish, whitish or yellowish. Some species have maculated, striped, doted leaves with several different colors.
• Generally their surfaces is glossy, occasionally the may have a dull appearance or even look like if recovered by white dust.

Some species are lacking chlorophylle. The majority of species keep their leaves duiring some years, but some loose them imediately after their seazonal growth period and other when environmental conditions are adverse. There are also nome genera whose leaves are just rudimentary, giving the impression to have only roots and eventual flowers. In these cases the roots usually have chlorophylle and are responsible for photosyntheses.

Inflorescence

Orchids inflorescences, according to the species, may have from one to some hundred flowers. They may be apical, lateral or basal, racemose or paniculated, forming branches, corymbes or umbellas, erect, arching or pending, with simultaneous or sucessive flowers, which can grow along the inflorescence or always from the same spot. Some species show perenial structures that are a sort of modified stem used only for blooming during several years, as it happens with some species of Masdevallia and all species of genus Psychopsis. The flowers generally have bracts at their bases. These bracts are variable in size, frequently highly reduced, may also be very large, looking to be part of the flower, as in some Cyrtopodium or sometimes even bigger and showyer than the flowers, which remain partially hidden by them, as in some Eria. The inflorescence from genus Dimorphorchis may be five meters long, with two different kinds of flowers spaced almost one meter each. Octomeria inflorescences just measure a couple of millimeters. The inflorescence of some orchid species grow down, thus when these are cultivated, they appear through the holes at the bottom of the pot.

Flowers

Among all plant families, orchids possibly are the ones of the widest spectrum of floral variation. Generally they have hermaphrodite flowers, but besides those, some genera in subtribe Catasetiinae may have exclusively male and female flowers, ocasionally showing a third type of flowers that can be hermaphodite at several degrees, sometimes resembling more male, sometimes more female. Interestingly enough, when these genera with dimorphic flowers produce hermaphodite ones, despite they are fertile, apparenly there is no natural pollinator for them.

The size of their flowers varies from two millimeters up to twenty centimeters, or even the double if the calcar of some orchid flowers is included. Ther colors range from almost translucent to white, greenish shades, pale pink or bluish to very vibrabt colors as yellow, orange, red and dark purple. Many are multicolored.

The flowers normally show bilateral simmetry, bearing six tepals split in two layers, three external called sepals and three internal denominated petals. Both the sepand and the petals are highly variable in shape and size, and ocasionally are partially or completely fused. One of the petals, denominated labellum, or informally as lip, always is differentiated, normally expanded but sometimes smaller than the rest of the segments, it may be very simple resembling one of the petals or may have calli, keels oe warts, highly variable and intrincate shapes with diverse and contrasting colors. In many genera the labellum shows an hollow tubular appendix at the base, called calcar, or a nectary close to the area where it is hinged or attached to the column. Observing the structures and patterns of the labellum is one of the most simple ways to recognize each of the orchid species.

Their reproductive organs, (androceu and gineceu), are reduced and fused into a single central structure called column, gymnostem or androstyle. The number of estamen varies among the subfamilies: Apostasioideae has two or three; Cypripedioideae has two, with the central estamen modified; the other subfamilies have just the central estamen is functional, and two other are atrofiated or absent. Also observing the characteristics of the column is important to correctly identify a particular species.

The pollen grains usually are compressed or aglutinated into waxy pellets called pollinia but alternatively may be grouped in mealy or paste-like doughs, or, hardly ever, loose. The pollinia are hinged by a thin connective rod structure called caudicle or stipe, according to its morphology, attached to a viscous disc called viscidium, hold in place by a thick liquid produced by the rostellum. Most of epiphytic species has a little helmet protectiong the pollinia denominated anther cap. The stigma normally is a cavity located at the column, partially filled with the same thick liquid the rostellum produces, where the pollinia are inserted by the pollinator when it visits the flower. The ovarium usually is composed by three chambers and bears up to circa one million eggs.

Fruit

Almost all orchid have capsular fruits. They are clearly different in shape, size and color. The epiphytes bear much thicker fruits with fleshy walls than terrestrial species which present them thiner with more delicate walls. Generally they are triangular, somewhat or highly rounded, with a variable number of keels, from three to nine. Some are smooth, other are wrinkly or covered with warts and protuberances all over their surfaces. The fruits result from the thickening of the ovarium located at the base of the flowers, which is also ordinarily formed by three chambers. When ripe, the fruit opens in three or six windows or almost enterely along its length, although always remaining attached to the inflorescence. Most of the seeds soon fall down, laying among the roots of mother plant, the rest is taken by the wind for long distances.

Seeds

Almost all orchids present light tiny seeds, formed by a a small number of covering cells protecting an embryo. One plant produces hundreds of thousands seeds each capsule. Contrary to most plants, which generaly produce endosperm capable of feeding the embryo during their initial period of development, orchids use a symbiotic proccess with the fungus Micorrhyza, which excretes the nutrients necessary to nourish the young plant decomposing the material gathered close to the seed. As soon as the embryo is capable of carrying photosyntheses, this becomes responsible for the nourishmento of the plant and the Micorrhyza is not necessary anymore, however, some species of saprophytic orchids will never be capable of fully carrying photosyntheses thus remain dependent upon this fungus for all their lives. Some species of orchids, as Bletilla do show some amount of endosperm. Few orchid species have comparetively large seeds, mostly the members of the subfamily Vanilloideae.

Pollination

The majority of other plants flowers try to attract pollinators offering rewards, mostly in form of food. Orchids, being plants that live from so sparse resources, need to be very economic so they developed other techniques of attraction which hardly include these food rewards. The most usual trick is the mimicry of any form that may interest to the insects and other agents, such as color, fragrances, or wax. They have also addapted their shapes in a way to ensure the pollinators to carry the pollen when they visit the flowers, although they adapted so perfectly that only the right visitor will adjust to the flower mechanics. Other visitors will not take the pollen away. This happens because all pollen is aggregated in masses that can only been taken once, thus each flower has one chance of pollination only. The labellum also helps a great deal on the proccess because they developed a variety of structures aiming to place the pollinator on the exact position to ensure that the pollinia they carry will reach the right spot into the flower stigma.

Hybrids

Fertile orchid hybrids can be artificialy crossed with other species of the same or of other genera and produce new generations of fertile hybrids. today there are hybrids involving up to eight genera and as time passes it is likely even more genera will be crossed. The Royal Horticultural Society is responsible for keeping the records of these hybrids up to date. The capacity orchids have to interbreed is one of their carachtheristics more valuated by growers because it enables them to mix the species obtaining endless combinations of new colors and patterns.