Product Code Database
Example Keywords: tetris -digital $34
   » » Wiki: Alveolate
Tag Wiki 'Alveolate'.
Tag

The alveolates (meaning "pitted like a honeycomb") are a group of , considered a major unranked or within . They are currently grouped with the and among the protists with tubulocristate mitochondria into the supergroup.


Characteristics
The most notable shared characteristic is the presence of cortical (near the surface) alveoli (sacs). These are flattened vesicles (sacs) arranged as a layer just under the and supporting it, typically contributing to a flexible pellicle (thin skin). In armored they may contain stiff plates. Alveolates have with tubular cristae (), and cells often have pore-like intrusions through the cell surface. The group contains free-living and organisms, predatory , and organisms.

Almost all sequenced mitochondrial genomes of ciliates and apicomplexa are linear. The mitochondria almost all carry of their own but with greatly reduced genome sizes. Exceptions are which are left with only a , the circular mitochondrial genomes of and , and 's highly fragmented mitochondrial genome, consisting of 21 sequence blocks which recombine to produce longer segments.


History
The relationship of apicomplexa, dinoflagellates and ciliates had been suggested during the 1980s, and this was confirmed in the early 1990s by comparisons of ribosomal RNA sequences, most notably by Gajadhar et al. . Cavalier-Smith introduced the formal name Alveolata in 1991,
(1991). 9780198577478, Oxford University Press.
although at the time he considered the grouping to be a assemblage. Many biologists prefer the use of the colloquial name 'alveolate'.Kumar, S. & Rzhetsky, A. 1996. Evolutionary relationships of eukaryotic kingdoms. Journal of Molecular Evolution, 42: 183–193


Classification
Alveolata include around nine major and minor groups. They are diverse in form, and are known to be related by various ultrastructural and genetic similarities:

The Acavomonidia and Colponemidia were previously grouped together as colponemids, a taxon now split because each has a distinctive organization or ultrastructural identity. The Acavomonidia are closer to the dinoflagellate/perkinsid group than the Colponemidia are. As such, the informal term "colponemids", as it stands currently, covers two non-sister groups within Alveolata: the Acavomonidia and the Colponemidia.

The Apicomplexa and dinoflagellates may be more closely related to each other than to the ciliates. Both have , and most share a bundle or cone of at the top of the cell. In apicomplexans this forms part of a complex used to enter host cells, while in some colorless dinoflagellates it forms a peduncle used to ingest prey. Various other genera are closely related to these two groups, mostly flagellates with a similar apical structure. These include free-living members in and , and parasites in Perkinsus, , and the . In 2001, direct amplification of the gene in marine samples revealed the presence of two novel alveolate lineages, called group I and II. Group I has no cultivated relatives, while group II is related to the dinoflagellate parasite , which was classified until now in the dinoflagellate order.

Some studies suggested the , mostly parasites of marine invertebrates, might belong here, but they lack alveoli and are now placed among the .

The ellobiopsids are of uncertain relation within the alveolates. Silberman et al 2004 establish that the genus of ellobiopsids are alveolates using analysis, however no more certainty exists on their place.


Phylogeny
In 2017, Thomas Cavalier-Smith described the phylogeny of the Alveolata as follows:


Taxonomy
Alveolata Cavalier-Smith 1991 Alveolatobiontes


Development
The development of plastids among the alveolates is intriguing. Cavalier-Smith proposed the alveolates developed from a chloroplast-containing ancestor, which also gave rise to the (the hypothesis). Other researchers have speculated that the alveolates originally lacked plastids and possibly the dinoflagellates and Apicomplexa acquired them separately. However, it now appears that the alveolates, the dinoflagellates, the Chromerida and the acquired their plastids from a red alga with evidence of a common origin of this organelle in all these four clades.


Evolution
A Bayesian estimate places the evolution of the alveolate group at ~. The Alveolata consist of , , and Colponemids. In other words, the term Myzozoa, meaning "to siphon the contents from prey", may be applied informally to the common ancestor of the subset of alveolates that are neither ciliates nor colponemids. Predation upon algae is an important driver in alveolate evolution, as it can provide sources for endosymbiosis of novel plastids. The term Myzozoa is therefore a handy concept for tracking the history of the alveolate phylum.

The ancestors of the alveolate group may have been photosynthetic. The ancestral alveolate probably possessed a . Chromerids, apicomplexans, and peridinin dinoflagellates have retained this . Going one step even further back, the chromerids, the peridinin dinoflagellates and the have been argued to possess a monophyletic plastid lineage in common, i.e. acquired their plastids from a , and so it seems likely that the common ancestor of alveolates and heterokonts was also photosynthetic.

In one school of thought the common ancestor of the , , , , and was a myzocytotic predator with two heterodynamic , , , , , a polar ring and a coiled open sided . While the common ancestor of alveolates may also have possessed some of these characteristics, it has been argued that Myzocytosis was not one of these characteristics, as ciliates ingest prey by a different mechanism.

An ongoing debate concerns the number of membranes surrounding the plastid across apicomplexans and certain dinoflagellates, and the origin of these membranes. This ultrastructural character can be used to group organisms and if the character is in common, it can imply that phyla had a common photosynthetic ancestor. On the basis that apicomplexans possess a plastid surrounded by four membranes, and that peridinin dinoflagellates possess a plastid surrounded by three membranes, Petersen et al. have been unable to rule out that the shared stramenopile-alveolate plastid could have been recycled multiple times in the alveolate phylum, the source being stramenopile-alveolate donors, through the mechanism of ingestion and .

Ciliates are a model alveolate, having been genetically studied in great depth over the longest period of any alveolate lineage. They are unusual among eukaryotes in that reproduction involves a and a . Their reproduction is easily studied in the lab, and made them a model eukaryote historically. Being entirely predatory and lacking any remnant plastid, their development as a phylum illustrates how predation and autotrophy are in dynamic balance and that the balance can swing one way or other at the point of origin of a new phylum from mixotrophic ancestors, causing one ability to be lost.

File:Paramecium caudatum Ehrenberg, 1833.jpg| () File:Mikrofoto.de-Glockentierchen-1.jpg| () (left) File:Plasmodium.jpg| Plasmodium falciparum () in blood File:Emaxima oocysts usda.jpg| () File:Dinophysis acuminata.jpg| ()


Epigenetics
Few have been studied for . Those for which epigenetic data are available include some algal alveolates.
(2025). 9781119821915, Wiley.


External links

Page 1 of 1
1
Page 1 of 1
1

Account

Social:
Pages:  ..   .. 
Items:  .. 

Navigation

General: Atom Feed Atom Feed  .. 
Help:  ..   .. 
Category:  ..   .. 
Media:  ..   .. 
Posts:  ..   ..   .. 

Statistics

Page:  .. 
Summary:  .. 
1 Tags
10/10 Page Rank
5 Page Refs
1s Time