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Vorticella | |
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Vorticella convallaria as illustrated by C.G. Ehrenberg in 1838 | |
Scientific classification | |
Domain: | Eukaryota |
Clade: | Diaphoretickes |
Clade: | SAR |
Clade: | Alveolata |
Phylum: | Ciliophora |
Class: | Oligohymenophorea |
Order: | Sessilida |
Family: | Vorticellidae |
Genus: | Vorticella L. (1767) |
Species | |
See text |
Vorticella is a genus of bell-shaped ciliates that have stalks to attach themselves to substrates. The stalks have contractile myonemes, allowing them to pull the cell body against substrates. [1] The formation of the stalk happens after the free-swimming stage. [2]
The organism is named Vorticella due to the beating cilia creating whirlpools, or vortices. It is also known as the “Bell Animalcule” due to its bell-shaped body. [3]
Vorticella was first described by Antonie van Leeuwenhoek in a letter dated October 9, 1676. Leeuwenhoek thought that Vorticella had two horns moving like horse ears near the oral part, which turned out to be oral cilia beating to create water flow. [4] In 1755, German miniature painter August Johann Rösel described Vorticella, which was named Hydra convallaria by Linnaeus in 1758. However, in 1767, it was renamed Vorticella convallaria. Otto Friedrich Müller listed 127 species of Vorticella in 1786, but many are now known to actually be other protozoans or rotifers. The definition of Vorticella that is still used today was first given by Ehrenberg in 1838. Since then, 80 more species have been described, although many may be synonyms of earlier species. [5]
Habitats may include moist soil, mud and plant roots. [6] This protozoan is ciliated and is mainly found in fresh water environments. [7] They are known to feed on bacteria and can also form extracellular associations with mosquitoes, nematodes, prawns and tadpoles. [6] Vorticella has been found as an epibiont (attached to the surface of a living substratum when in its sessile stage) of crustaceans, the basibiont. This relationship between the epibiont and basibiont is called epibiosis. [8] Rotifers have been observed to feed on Vorticella. Bacteria may also live attached to the surface of Vorticella cells as epibionts, [5] which in some cases may represent a symbiotic relationship between the ciliate and bacteria. [9]
These solitary organisms have globulous bodies which are oval-shaped when contracted. [8] Unfavourable conditions tend to cause Vorticella to change from long and skinny to short and wide. [5] The oral cavity is at one end while the stalk is at the other. [6] The body is 30-40 micrometers in diameter contracted and the stalk is 3-4 micrometers in diameter and 100 micrometers long. [4]
The protoplasm of Vorticella is typically a translucent blue-white colour, but may contain a yellow or green pigment. The food vacuoles may show as a brown or grey colour, but depends on the food eaten. Zoochlorellae, food reserves and waste granules, which are abundant in the cytoplasm, may create the impression that Vorticella is an opaque cell. [5]
Vorticella has a pellicle with striae running parallel around the cell. This pellicle may be decorated with pustules, warty projections, spines or tubercules. Harmless or parasitic bacteria may grow on the body or stalk, appearing as part of the morphology of the cell. [5] Inside, there is a curved, transverse macronucleus and round micronucleus near it.
The similar genus Pseudovorticella is practically indistinguishable from Vorticella under most conditions. The two genera differ in their infraciliature, which can be made visible with silver staining: Pseudovorticella has a mesh-like pattern on the surface of the cell. [10]
During its motile form, the free-swimming telotroch appears as a long cylinder, moving quickly and erratically. Stalk materials are secreted in order for the cell to become sessile. Stalk precursors are held in dense granules at the aboral or basal end of the telotroch, which are released as a liquid by exocytosis. That liquid solidifies to form the adhesion pad, stalk matrix and stalk sheath. The stalk will finish growing in several hours. [2]
The stalk is made up of the spasmoneme, a contractile organelle, with rigid rod filaments, batonnets, surrounding it. The coiled spasmoneme and batonnets serve as a molecular spring, so that Vorticella can contract. The cell body can move hundreds of micrometers in milliseconds. The spasmoneme is said to have higher specific power than the engine of the average car. [7]
Vorticella has an anterior peristomial lip which is short and narrow. An outward-curving peristomial disc is associated with the peristome. [8] The peristomial disc, which may have ringed ridges or undulations, encloses rows of cilia. The contractile peristomal border closes over the disc and cilia during retraction of Vorticella. [5]
Vorticella is a suspension feeder, and may have reduced or no cytopharynxes, a nonciliated tube for ingestion. There are oral cilia specialized for making water currents, cytostomes in a depression on the cell surface and structures for scraping and filtering food. [1] Oral cilia beat to bring food closer at speeds of 0.1–1 mm/s. [4]
Water flowing inwards brings food through the vestibule, between the inner and outer membranes. The vestibule is a passage for both food entrance and waste exit. The vestibular membranes push the food inwards, where they then congregate in a spindle-shaped food vacuole in the pharynx. Once the food vacuoles leave the non-ciliated pharyngeal tube, they become rounded. When the water flows outwards, contractile vacuoles and full food vacuoles may empty their contents. Contractile vacuoles are located between or beside the macronucleus and vestibule. [5]
The oral cilia contain the adoral zone of membranelles (AZM), which are compound ciliary organelles. The paroral membrane consists of a row of paired cilia. The cytostome has the AZM on one side and the paroral membrane on the other side. [1] As adults, they do not have somatic cilia. [8] In terms of reproduction, Vorticella can undergo binary fission. [1] This occurs when the organism splits into two parts, with the division going along the length of the organism (“The Vorticella” 1885).
A fossil Vorticella has been discovered inside a leech cocoon dating to the Triassic period, ca. 200 million years ago. The fossil was recovered from the Section Peak Formation at Timber Peak in East Antarctica, and has a recognizable peristome, helically-contractile stalk, and C-shaped macronucleus, like modern Vorticella species. [11]
The growth, development and emergence of mosquito larvae are inhibited by Vorticella, resulting in death. The biopolymer glue used for attachment to surfaces may damage sensory systems or pore formation of larvae. Another possibility is that the larvae die by being unable to remain on the surface of the water, thus drowning. Vorticella has for this reason, been explored as a method of biocontrol for mosquitoes, which are vectors of pathogenic, tropical diseases. [6]
Over 200 species of Vorticella have been described, although many may be synonyms. [12] Molecular phylogenetics shows that some species that were previously considered to be Vorticella because of their morphology actually belong to another group, forming a clade with the swimming peritrichs Astylozoon and Opisthonecta . [13]
The peritrichs are a large and distinctive group of ciliates.
Paramecium is a genus of eukaryotic, unicellular ciliates, commonly studied as a model organism of the ciliate group. Paramecium are widespread in freshwater, brackish, and marine environments and are often abundant in stagnant basins and ponds. Because some species are readily cultivated and easily induced to conjugate and divide, they have been widely used in classrooms and laboratories to study biological processes. The usefulness of Paramecium as a model organism has caused one ciliate researcher to characterize it as the "white rat" of the phylum Ciliophora.
Suctoria are ciliates that become sessile in their developed stage and then lose their redundant cilia. They feed by extracellular digestion. They were originally thought to feed by suction – hence their name. In fact, they use specialized microtubules to ensnare and manipulate their prey. They live in both freshwater and marine environments, including some that live on the surface of aquatic animals, and typically feed on other ciliates. Instead of a single cytostome, each cell feeds by means of several specialized tentacles. These are supported by microtubules and phyllae, and have toxic extrusomes called haptocysts at the tip, which they attach to prey. They then suck the prey's cytoplasm directly into a food vacuole inside the cell, where they digest and absorb its contents. Most suctoria are around 15-30 μm in size, with a non-contractile stalk and often a lorica or shell.
Balantidium coli is a parasitic species of ciliate alveolates that causes the disease balantidiasis. It is the only member of the ciliate phylum known to be pathogenic to humans.
Stylonychia is a genus of ciliates, in the subclass Hypotrichia. Species of Stylonychia are very common in fresh water and soil, and may be found on filamentous algae, surface films, and among particles of sediment. Like other Hypotrichs, Stylonychia has cilia grouped into membranelles alongside the mouth and cirri over the body. It is distinguished partly by long cirri at the posterior, usually a cluster of three. The largest can just be seen at a 25x magnification, and the smallest can just be seen at a 450x magnification.
Spirostomum is a genus of ciliated protists in the class Heterotrichea. It is known for being very contractile. Having been first identified by Christian Gottfried Ehrenberg in 1834, further research has identified eight additional true morphospecies. This bacterivore genus mainly lives in the sediment deposits at the bottom of various aquatic habitats, and members possess rquA genes that could be responsible for their ability to survive in these hypoxic and anoxic environments. They are identifiable by their relatively large tubular/flat vermiform bodies. Their life cycle consists of a growth stage, in which they mature, and asexual and sexual reproduction stages. Some species are model organisms for studies on human pathogenic bacteria, while others are sensitive and accurate bioindicators for toxic substances.
Paramecium caudatum is a species of unicellular protist in the phylum Ciliophora. They can reach 0.33 mm in length and are covered with minute hair-like organelles called cilia. The cilia are used in locomotion and feeding. The species is very common, and widespread in marine, brackish and freshwater environments.
Vorticella convallaria is a species of ciliates. It is the type species of the genus Vorticella. It resembles V. campanula, but differs in being somewhat narrow in the anterior end and usually having no refractile granules in the endoplasm.
Trichodina is a genus of ciliate alveolates that is ectocommensal or parasitic on aquatic animals, particularly fish. They are characterised by the presence of a ring of interlocking cytoskeletal denticles, which provide support for the cell and allow for adhesion to surfaces including fish tissue.
The ciliates are a group of alveolates characterized by the presence of hair-like organelles called cilia, which are identical in structure to eukaryotic flagella, but are in general shorter and present in much larger numbers, with a different undulating pattern than flagella. Cilia occur in all members of the group and are variously used in swimming, crawling, attachment, feeding, and sensation.
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Pseudomonilicaryon anser is a species of unicellular ciliates in the family Dileptidae, also known under the names Dileptus anser and Dileptus cygnus. The species is common in fresh water ponds, stagnant pools, mosses and soils.
Colpoda inflata is a unicellular organism, belonging to the genus Colpoda. Colpodeans are eucaryotic protozoans, that mainly feed on bacteria (bacteriophagous), vary a lot in size and have a funnel-shaped vestibule.
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Cothurnia is a genus of freshwater and marine peritrichs in the family Vaginicolidae. It is characterised by living in a transparent tubular lorica. During the feeding or vegetative phase of its life cycle, Cothurnia attaches to submerged surfaces through a short stalk — mostly on the surfaces of fishes, crustaceans and aquatic plants. It is commonly studied for its epibiotic relationship with the host that it is attached to.
Zoothamnium niveum is a species of ciliate protozoan which forms feather-shaped colonies in marine coastal environments. The ciliates form a symbiosis with sulfur-oxidizing chemosynthetic bacteria of the species "Candidatus Thiobios zoothamnicoli", which live on the surface of the colonies and give them their unusual white color.
Zoothamnium is a genus of ciliate protozoan.
Stentor roeselii is a free-living ciliate species of the genus Stentor, in the class Heterotrichea. It is a common and widespread protozoan, found throughout the world in freshwater ponds, lakes, rivers and ditches.
Halteria, sometimes referred to as the jumping oligotrich, is a genus of common planktonic ciliates that are found in many freshwater environments. Halteria are easy to locate due to their abundance and distinctive behaviour with observations of Halteria potentially dating back to the 17th century and the discovery of microorganisms. Over time more has been established about their morphology and behavior, which has led to many changes in terms of classification.
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