Alga in the context of Microalgae

Chlorophyll is any of several related green pigments found in cyanobacteria and in the chloroplasts of algae and plants. Its name is derived from the Greek words χλωρός (khloros, "pale green") and φύλλον (phyllon, "leaf"). Chlorophyll allows plants to absorb energy from light. Those pigments are involved in oxygenic photosynthesis, as opposed to bacteriochlorophylls, related molecules found only in bacteria and involved in anoxygenic photosynthesis.

Chlorophylls absorb light most strongly in the blue portion of the electromagnetic spectrum as well as the red portion. Conversely, it is a poor absorber of green and near-green portions of the spectrum. Hence chlorophyll-containing tissues appear green because green light, diffusively reflected by structures like cell walls, is less absorbed. Two types of chlorophyll exist in the photosystems of green plants: chlorophyll a and b.

A halophile (from the Greek word for 'salt-loving') is an extremophile that thrives in high salt concentrations. In chemical terms, halophile refers to a Lewis acidic species that has some ability to extract halides from other chemical species.

While most halophiles are classified into the domain Archaea, there are also bacterial halophiles and some eukaryotic species, such as the alga Dunaliella salina and fungus Wallemia ichthyophaga. Some well-known species give off a red color from carotenoid compounds, notably bacteriorhodopsin.

Bacteriochlorophylls (BChl) are photosynthetic pigments that occur in various phototrophic bacteria. They were discovered by C. B. van Niel in 1932. They are related to chlorophylls, which are the primary pigments in plants, algae, and cyanobacteria. Organisms that contain bacteriochlorophyll conduct photosynthesis to sustain their energy requirements, but the process is anoxygenic and does not produce oxygen as a byproduct. They use wavelengths of light not absorbed by plants or cyanobacteria. Replacement of Mg with protons gives bacteriophaeophytin (BPh), the phaeophytin form.

• Structures of major bacteriochlorophylls
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  bacteriochlorophyll a
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  bacteriochlorophyll b
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  bacteriochlorophyll c
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  bacteriochlorophyll d
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  bacteriochlorophyll e
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  bacteriochlorophyll f
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  bacteriochlorophyll g

The chlorarachniophytes are a small group of exclusively marine algae widely distributed in tropical and temperate waters. They are typically mixotrophic, ingesting bacteria and smaller protists as well as conducting photosynthesis. Normally they have the form of small amoebae, with branching cytoplasmic extensions that capture prey and connect the cells together, forming a net. These extensions are dependent on the presence of light and polymerization of the actin cytoskeleton. They may also form flagellate zoospores, which characteristically have a single subapical flagellum that spirals backwards around the cell body, and walled coccoid cells.

The chloroplasts were presumably acquired by ingesting some green alga. They are surrounded by four membranes, the outermost of which is continuous with the endoplasmic reticulum, and contain a small nucleomorph between the middle two, which is a remnant of the alga's nucleus. This contains a small amount of DNA and divides without forming a mitotic spindle. The origin of the chloroplasts from green algae is supported by their pigmentation, which includes chlorophylls a and b, and by genetic similarities. The only other groups of algae that contain nucleomorphs are a few species of dinoflagellates, which also have plastids originating from green algae, and the cryptomonads, which acquired their chloroplasts from a red alga.

An epiphyte (from Ancient Greek epi-, meaning 'upon', and phutón, meaning 'plant') is a plant or plant-like organism that grows on the surface of another plant or plant-like organism such as kelp. It derives its moisture and nutrients from the air, rain, water (in marine environments) or from debris accumulating around it. The plants on which epiphytes grow are called phorophytes. Epiphytes take part in nutrient cycles and add to both the diversity and biomass of the ecosystem in which they occur, like any other organism. In some cases, a rainforest tree's epiphytes may weigh several tonnes. Epiphytes differ from parasitic plants in that they grow on the host for physical support only, and do not draw nourishment from it. An organism that grows on another organism that is not a plant may be called an epibiont. Epiphytes are usually found in the temperate zone (e.g., many mosses, liverworts, lichens, and algae) or in the tropics (e.g., many ferns, cacti, orchids, and bromeliads). Epiphyte species make good houseplants due to their minimal water and soil requirements. Epiphytes provide a rich and diverse habitat for other organisms including animals, fungi, bacteria, and myxomycetes.

Epiphyte is one of the subdivisions of the Raunkiær system.The term epiphytic derives from Greek epi- 'upon' and phyton 'plant'. Epiphytic plants are sometimes called "air plants" because they do not root in soil. However, that term is inaccurate, as there are many aquatic species of algae that are epiphytes on other aquatic plants (seaweeds or aquatic angiosperms).

Lichens are symbiotic organisms made up of multiple species: a fungus, one or more photobionts (an alga and/or a cyanobacteria) and sometimes a yeast. They are regularly grouped by their external appearance – a characteristic known as their growth form. This form, which is based on the appearance of vegetative part of the lichen (its thallus), varies depending on the species and the environmental conditions it faces. Those who study lichens (lichenologists) have described a dozen of these forms: areolate, byssoid, calicioid, cladoniform, crustose, filamentous, foliose, fruticose, gelatinous, leprose, placodioid and squamulose. Traditionally, crustose (flat), foliose (leafy) and fruticose (shrubby) are considered to be the three main forms. In addition to these more formalised, traditional growth types, there are a handful of informal types named for their resemblance to the lichens of specific genera. These include alectorioid, catapyrenioid, cetrarioid, hypogymnioid, parmelioid and usneoid.

An antheridium is a haploid structure or organ producing and containing male gametes (called antherozoids or sperm). The plural form is antheridia, and a structure containing one or more antheridia is called an androecium.

Antheridia are present in the gametophyte phase of cryptogams like bryophytes and ferns. Many algae and some fungi, for example, ascomycetes and water moulds, also have antheridia during their reproductive stages. In gymnosperms and angiosperms, the male gametophytes have been reduced to pollen grains, and in most of these, the antheridia have been reduced to a single generative cell within the pollen grain. During pollination, this generative cell divides and gives rise to sperm cells.

A sporeling is a young plant or fungus produced by a germinated spore, similar to a seedling derived from a germinated seed. They occur in algae, fungi, lichens, bryophytes and seedless vascular plants.

In ecology, a cascade effect is a series of secondary extinctions that are triggered by the primary extinction of a key species in an ecosystem. Secondary extinctions are likely to occur when the threatened species are: dependent on a few specific food sources, mutualistic (dependent on the key species in some way), or forced to coexist with an invasive species that is introduced to the ecosystem. Species introductions to a foreign ecosystem can often devastate entire communities, and even entire ecosystems. These exotic species monopolize the ecosystem's resources, and since they have no natural predators to decrease their growth, they are able to increase indefinitely. Olsen et al. showed that exotic species have caused lake and estuary ecosystems to go through cascade effects due to loss of algae, crayfish, mollusks, fish, amphibians, and birds. However, the principal cause of cascade effects is the loss of top predators as the key species. As a result of this loss, a dramatic increase (ecological release) of prey species occurs. The prey is then able to overexploit its own food resources, until the population numbers decrease in abundance, which can lead to extinction. When the prey's food resources disappear, they starve and may go extinct as well. If the prey species is herbivorous, then their initial release and exploitation of the plants may result in a loss of plant biodiversity in the area. If other organisms in the ecosystem also depend upon these plants as food resources, then these species may go extinct as well. An example of the cascade effect caused by the loss of a top predator is apparent in tropical forests. When hunters cause local extinctions of top predators, the predators' prey's population numbers increase, causing an overexploitation of a food resource and a cascade effect of species loss. Recent studies have been performed on approaches to mitigate extinction cascades in food-web networks.

Nannochloropsis is a genus of algae comprising six known species. The genus in the current taxonomic classification was first termed by Hibberd (1981). The species have mostly been known from the marine environment but also occur in fresh and brackish water. All of the species are small, nonmotile spheres which do not express any distinct morphological features that can be distinguished by either light or electron microscopy. The characterisation is mostly done by rbcL gene and 18S rRNA sequence analysis.

The algae of the genus Nannochloropsis differ from other related microalgae in that they have chlorophyll a and completely lack chlorophyll b and chlorophyll c. In addition they are able to build up a high concentrations of a range of pigments such as astaxanthin, zeaxanthin and canthaxanthin. They have a diameter of about 2 to 3 micrometers and a very simple ultrastructure with reduced structural elements compared to neighbouring taxa.

Hexachara is a genus of fossil charophyte (aquatic green alga) that is likely to have formed meadows within sheltered oligohaline reaches of lakes.

90°00′S 0°00′W / 90.000°S -0.000°E / -90.000; -0.000

The Antarctic realm is one of eight terrestrial biogeographic realms. The ecosystem includes Antarctica and several island groups in the southern Atlantic and Indian oceans. The continent of Antarctica is so cold that it has supported only 2 vascular plants for millions of years, and its flora presently consists of around 250 lichens, 100 mosses, 25–30 liverworts, and around 700 terrestrial and aquatic algal species, which live on the areas of exposed rock and soil around the shore of the continent. Antarctica's two flowering plant species, the Antarctic hair grass (Deschampsia antarctica) and Antarctic pearlwort (Colobanthus quitensis), are found on the northern and western parts of the Antarctic Peninsula. Antarctica is also home to a diversity of animal life, including penguins, seals, and whales.

Lichenology is the branch of mycology that studies the lichens, symbiotic organisms made up of an intimate symbiotic association of a microscopic alga (or a cyanobacterium) with a filamentous fungus. Lichens are chiefly characterized by this symbiosis.

Study of lichens draws knowledge from several disciplines: mycology, phycology, microbiology and botany. Scholars of lichenology are known as lichenologists. Study of lichens is conducted by both professional and amateur lichenologists.

A gemma (English plural gemmas, Latin plural gemmae) is a single cell, or a mass of cells, or a modified bud of tissue, that detaches from the parent and develops into a new individual. This type of asexual reproduction is referred to as fragmentation. It is a means of asexual propagation in plants. These structures are commonly found in fungi, algae, liverworts and mosses, but also in some flowering plants such as pygmy sundews and some species of butterworts. Vascular plants have many other methods of asexual reproduction including bulbils and turions.

Biofouling or biological fouling is the accumulation of microorganisms, plants, algae, or small animals where it is not wanted on surfaces such as ship and submarine hulls, devices such as water inlets, pipework, grates, ponds, and rivers that cause degradation to the primary purpose of that item. Such accumulation is referred to as epibiosis when the host surface is another organism and the relationship is not parasitic. Since biofouling can occur almost anywhere water is present, biofouling poses risks to a wide variety of objects such as boat hulls and equipment, medical devices and membranes, as well as to entire industries, such as paper manufacturing, food processing, underwater construction, and desalination plants.

Anti-fouling is the ability of specifically designed materials (such as toxic biocide paints, or non-toxic paints) to remove or prevent biofouling.