The dinoflagellates (Greek
δῖνος ''dinos'' "whirling" and Latin
''flagellum'' "whip, scourge") are single-celled eukaryotes
constituting the phylum Dinoflagellata.
Usually considered algae
, dinoflagellates are mostly marine plankton
, but they also are common in freshwater habitats
. Their populations are distributed depending on sea surface temperature
, or depth. Many dinoflagellates are known to be photosynthetic
, but a large fraction of these are in fact mixotrophic
, combining photosynthesis with ingestion of prey (phagotrophy
In terms of number of species, dinoflagellates are one of the largest groups of marine eukaryotes, although this group is substantially smaller than diatom
s. Some species are endosymbiont
s of marine animals and play an important part in the biology of coral reef
s. Other dinoflagellates are unpigmented predators on other protozoa, and a few forms are parasitic
(for example, ''Oodinium
'' and ''Pfiesteria
''). Some dinoflagellates produce resting stages, called dinoflagellate cysts or dinocyst
s, as part of their lifecycles, and is known from 84 of the 350 described freshwater species, and from a little more than 10% of the known marine species. Dinoflagellates are alveolates
possessing two flagella
, the ancestral condition of bikonts
About 1,555 species of free-living marine dinoflagellates are currently described.
Another estimate suggests about 2,000 living species, of which more than 1,700 are marine (free-living, as well as benthic) and about 220 are from fresh water. The latest estimates suggest a total of 2,294 living dinoflagellate species, which includes marine, freshwater, and parasitic dinoflagellates.
A rapid accumulation of certain dinoflagellates can result in a visible coloration of the water, colloquially known as red tide
(a harmful algal bloom
), which can cause shellfish poisoning
if humans eat contaminated shellfish. Some dinoflagellates also exhibit bioluminescence
—primarily emitting blue-green light. Thus, some parts of the Indian Ocean light up at night giving blue-green light.
In 1753, the first modern dinoflagellates were described by Henry Baker
as "Animalcules which cause the Sparkling Light in Sea Water", and named by Otto Friedrich Müller
in 1773. The term derives from the Greek word δῖνος (''dinos''), meaning whirling, and Latin ''flagellum'', a diminutive term for a whip or scourge.
In the 1830s, the German microscopist Christian Gottfried Ehrenberg
examined many water and plankton samples and proposed several dinoflagellate genera that are still used today including ''Peridinium, Prorocentrum'', and ''Dinophysis''.
These same dinoflagellates were first defined by Otto Bütschli
in 1885 as the flagellate
order Dinoflagellida. Botanists treated them as a division of algae, named Pyrrophyta or Pyrrhophyta ("fire algae"; Greek ''pyrr(h)os'', fire) after the bioluminescent forms, or Dinophyta. At various times, the cryptomonad
s, and ellobiopsid
s have been included here, but only the last are now considered close relatives. Dinoflagellates have a known ability to transform from noncyst to cyst-forming strategies, which makes recreating their evolutionary history extremely difficult.
Dinoflagellates are unicellular and possess two dissimilar flagella arising from the ventral cell side (dinokont flagellation). They have a ribbon-like transverse flagellum with multiple waves that beats to the cell's left, and a more conventional one, the longitudinal flagellum, that beats posteriorly. The transverse flagellum is a wavy ribbon in which only the outer edge undulates from base to tip, due to the action of the axoneme which runs along it. The axonemal edge has simple hairs that can be of varying lengths. The flagellar movement produces forward propulsion and also a turning force. The longitudinal flagellum is relatively conventional in appearance, with few or no hairs. It beats with only one or two periods to its wave. The flagella lie in surface grooves: the transverse one in the cingulum and the longitudinal one in the sulcus, although its distal portion projects freely behind the cell. In dinoflagellate species with desmokont flagellation (e.g., ''Prorocentrum''), the two flagella are differentiated as in dinokonts, but they are not associated with grooves.
Dinoflagellates have a complex cell covering called an amphiesma or cortex, composed of a series of membranes, flattened vesicle
s called alveolae (= amphiesmal vesicles) and related structures.
[ In ]
In armoured dinoflagellates, these support overlapping cellulose
plates to create a sort of armor called the theca or lorica, as opposed to athecate dinoflagellates. These occur in various shapes and arrangements, depending on the species and sometimes on the stage of the dinoflagellate. Conventionally, the term tabulation has been used to refer to this arrangement of thecal plates. The plate configuration can be denoted with the plate formula or tabulation formula. Fibrous extrusome
s are also found in many forms. Together with various other structural and genetic details, this organization indicates a close relationship between the dinoflagellates, the Apicomplexa
, and ciliate
s, collectively referred to as the alveolate
Dinoflagellate tabulations can be grouped into six "tabulation types": gymnodinoid
, and prorocentroid
s in most photosynthetic dinoflagellates are bound by three membrane
s, suggesting they were probably derived from some ingested algae
. Most photosynthetic species contain chlorophyll
s ''a'' and c2, the carotenoid beta-carotene, and a group of xanthophylls that appears to be unique to dinoflagellates, typically peridinin
, dinoxanthin, and diadinoxanthin. These pigments give many dinoflagellates their typical golden brown color. However, the dinoflagellates ''Karenia brevis
, Karenia mikimotoi
,'' and ''Karlodinium micrum
'' have acquired other pigments through endosymbiosis, including fucoxanthin
This suggests their chloroplasts were incorporated by several endosymbiotic events involving already colored or secondarily colorless forms. The discovery of plastids in the Apicomplexa has led some to suggest they were inherited from an ancestor common to the two groups, but none of the more basal lines has them.
All the same, the dinoflagellate cell consists of the more common organelles such as rough and smooth endoplasmic reticulum, Golgi apparatus, mitochondria, lipid and starch grains, and food vacuoles. Some have even been found with a light-sensitive organelle, the eyespot or stigma, or a larger nucleus containing a prominent nucleolus. The dinoflagellate ''Erythropsidium
'' has the smallest known eye.
Some athecate species have an internal skeleton consisting of two star-like siliceous elements that has an unknown function, and can be found as microfossils
. Tappan gave a survey of dinoflagellates with internal skeletons. This included the first detailed description of the pentasters
in ''Actiniscus pentasterias'', based on scanning electron microscopy. They are placed within the order Gymnodiniales, suborder Actiniscineae.
Theca structure and formation
The formation of thecal plates has been studied in detail through ultrastructural studies.
The dinoflagellate nucleus: dinokaryon
'Core dinoflagellates' (dinokaryotes
) have a peculiar form of nucleus
, called a dinokaryon
, in which the chromosome
s are attached to the nuclear membrane. These carry reduced number of histone
s. In place of histones, dinoflagellate nuclei contain a novel, dominant family of nuclear proteins that appear to be of viral origin, thus are called Dinoflagellate viral nucleoprotein
s (DVNPs) which are highly basic, bind DNA with similar affinity to histones, and occur in multiple posttranslationally modified forms. Dinoflagellate nuclei remain condensed throughout interphase rather than just during mitosis
, which is closed and involves a uniquely extranuclear mitotic spindle
[ In ]
This sort of nucleus was once considered to be an intermediate between the nucleoid region of prokaryote
s and the true nuclei of eukaryote
s, so were termed mesokaryotic, but now are considered derived rather than primitive traits (i.e. ancestors of dinoflagellates had typical eukaryotic nuclei). In addition to dinokaryotes, DVNPs can be found in a group of basal dinoflagellates (known as Marine Alveolate
s, "MALVs") that branch as sister to dinokaryotes (Syndiniales
Dinoflagellates are protists which have been classified using both the International Code of Botanical Nomenclature
(ICBN, now renamed as ICN) and the International Code of Zoological Nomenclature
(ICZN). About half of living dinoflagellate species are autotrophs possessing chloroplasts and half are nonphotosynthesising heterotrophs.
The peridinin dinoflagellates, named after their peridinin plastids, appears to be ancestral for the dinoflagellate lineage. Almost half of all known species have chloroplasts, which are either the original peridinin plastids or new plastids acquired from other lineages of unicellular algae through endosymbiosis. The remaining species have lost their photosynthetic abilities and have adapted to a heterotrophic, parasitic or kleptoplastic
Most (but not all) dinoflagellates have a dinokaryon
, described below (see: Life cycle
, below). Dinoflagellates with a dinokaryon are classified under Dinokaryota
, while dinoflagellates without a dinokaryon are classified under Syndiniales
Although classified as eukaryotes
, the dinoflagellate nuclei are not characteristically eukaryotic, as some of them lack histones
, and maintain continually condensed chromosomes during mitosis
. The dinoflagellate nucleus was termed ‘mesokaryotic’ by Dodge (1966), due to its possession of intermediate characteristics between the coiled DNA areas of prokaryotic bacteria and the well-defined eukaryotic nucleus. This group, however, does contain typically eukaryotic organelles
, such as Golgi bodies, mitochondria, and chloroplasts.
Jakob Schiller (1931–1937) provided a description of all the species, both marine and freshwater, known at that time. Later, Alain Sournia (1973, 1978, 1982, 1990, 1993) listed the new taxonomic entries published after Schiller (1931–1937). Sournia (1986) gave descriptions and illustrations of the marine genera of dinoflagellates, excluding information at the species level. The latest index is written by Gómez.
English-language taxonomic monographs covering large numbers of species are published for the Gulf of Mexico, the Indian Ocean, the British Isles, the Mediterranean and the North Sea.
The main source for identification of freshwater dinoflagellates is the ''Süsswasser Flora''.
can be used to stain thecal plates in armoured dinoflagellates.
Ecology and physiology
Dinoflagellates can occur in all aquatic environments: marine, brackish, and fresh water, including in snow or ice. They are also common in benthic environments and sea ice.
are dinoflagellates and most of them are members within Symbiodiniaceae (e.g. the genus ''Symbiodinium
''). The association between ''Symbiodinium'' and reef-building coral
s is widely known. However, endosymbiontic Zooxanthellae
inhabit a great number of other invertebrates and protists, for example many sea anemones
, the giant clam ''Tridacna
'', and several species of radiolarians
. Many extant dinoflagellates are parasites
(here defined as organisms that eat their prey from the inside, i.e. endoparasites
, or that remain attached to their prey for longer periods of time, i.e. ectoparasites). They can parasitize animal or protist hosts. ''Protoodinium, Crepidoodinium, Piscinoodinium'', and ''Blastodinium'' retain their plastids while feeding on their zooplanktonic or fish hosts. In most parasitic dinoflagellates, the infective stage resembles a typical motile dinoflagellate cell.
Three nutritional strategies are seen in dinoflagellates: phototroph
y, and heterotroph
y. Phototrophs can be photoautotroph
s or auxotrophs
. Mixotrophic dinoflagellates
are photosynthetically active, but are also heterotrophic. Facultative mixotrophs, in which autotrophy or heterotrophy is sufficient for nutrition, are classified as amphitrophic. If both forms are required, the organisms are mixotrophic ''sensu stricto''. Some free-living dinoflagellates do not have chloroplasts, but host a phototrophic endosymbiont. A few dinoflagellates may use alien chloroplasts (cleptochloroplasts), obtained from food (kleptoplasty
). Some dinoflagellates may feed on other organisms as predators or parasites.
Food inclusions contain bacteria, bluegreen algae, small dinoflagellates, diatoms, ciliates, and other dinoflagellates.
Mechanisms of capture and ingestion in dinoflagellates are quite diverse. Several dinoflagellates, both thecate (e.g. ''Ceratium hirundinella'',
) and nonthecate (e.g. ''Oxyrrhis marina'',
''Gymnodinium'' sp. and ''Kofoidinium'' spp.), draw prey to the sulcal region of the cell (either via water currents set up by the flagella or via pseudopodial extensions) and ingest the prey through the sulcus. In several ''Protoperidinium'' spp., e.g. ''P. conicum'', a large feeding veil — a pseudopod called the pallium — is extruded to capture prey which is subsequently digested extracellularly
''Oblea'', ''Zygabikodinium'', and ''Diplopsalis'' are the only other dinoflagellate genera known to use this particular feeding mechanism.
''Katodinium (Gymnodinium) fungiforme'', commonly found as a contaminant in algal or ciliate cultures, feeds by attaching to its prey and ingesting prey cytoplasm through an extensible peduncle. Two related species, polykrikos kofoidii and neatodinium, shoots out a harpoon-like organelle to capture prey. The feeding mechanisms of the oceanic dinoflagellates remain unknown, although pseudopodial extensions were observed in ''Podolampas bipes''.
Dinoflagellate blooms are generally unpredictable, short, with low species diversity, and with little species succession.
The low species diversity can be due to multiple factors. One way a lack of diversity may occur in a bloom is through a reduction in predation and a decreased competition. The first may be achieved by having predators reject the dinoflagellate, by, for example, decreasing the amount of food it can eat. This additionally helps prevent a future increase in predation pressure by cause predators that reject it to lack the energy to breed. A species can then inhibit the growth of its competitors, thus achieving dominance.
Harmful algal blooms
Dinoflagellates sometimes bloom in concentrations of more than a million cells per millilitre. Under such circumstances, they can produce toxins (generally called dinotoxin
s) in quantities capable of killing fish and accumulating in filter feeders such as shellfish
, which in turn may be passed on to people who eat them. This phenomenon is called a red tide
, from the color the bloom imparts to the water. Some colorless dinoflagellates may also form toxic blooms, such as ''Pfiesteria
''. Some dinoflagellate blooms are not dangerous. Bluish flickers visible in ocean water at night often come from blooms of bioluminescent
dinoflagellates, which emit short flashes of light when disturbed.
The same red tide mentioned above is more specifically produced when dinoflagellates are able to reproduce rapidly and copiously on account of the abundant nutrients in the water. Although the resulting red waves are an unusual sight, they contain toxin
s that not only affect all marine life in the ocean, but the people who consume them, as well. A specific carrier is shellfish
. This can introduce both nonfatal and fatal illnesses. One such poison is saxitoxin
, a powerful paralytic neurotoxin
. Human inputs of phosphate
further encourage these red tides, so strong interest exists in learning more about dinoflagellates, from both medical and economic perspectives. Dinoflagellates are known to be particularly capable of scavenging dissolved organic phosphorus for P-nutrient, several HAS species have been found to be highly versatile and mechanistically diversified in utilizing different types of DOPs. The ecology of harmful algal blooms is extensively studied.
At night, water can have an appearance of sparkling light due to the bioluminescence of dinoflagellates. More than 18 genera of dinoflagellates are bioluminescent, and the majority of them emit a blue-green light. These species contain scintillons
, individual cytoplasmic bodies (about 0.5 µm in diameter) distributed mainly in the cortical region of the cell, outpockets of the main cell vacuole. They contain dinoflagellate luciferase
, the main enzyme involved in dinoflagellate bioluminescence, and luciferin
, a chlorophyll-derived tetrapyrrole ring that acts as the substrate to the light-producing reaction. The luminescence occurs as a brief (0.1 sec) blue flash (max 476 nm) when stimulated, usually by mechanical disturbance. Therefore, when mechanically stimulated—by boat, swimming, or waves, for example—a blue sparkling light can be seen emanating from the sea surface.
Dinoflagellate bioluminescence is controlled by a circadian clock and only occurs at night. Luminescent and nonluminescent strains can occur in the same species. The number of scintillons is higher during night than during day, and breaks down during the end of the night, at the time of maximal bioluminescence.
The luciferin-luciferase reaction responsible for the bioluminescence is pH sensitive.
When the pH drops, luciferase changes its shape, allowing luciferin, more specifically tetrapyrrole, to bind.
Dinoflagellates can use bioluminescence as a defense mechanism. They can startle their predators by their flashing light or they can ward off potential predators by an indirect effect such as the "burglar alarm". The bioluminescence attracts attention to the dinoflagellate and its attacker, making the predator more vulnerable to predation from higher trophic levels.
Bioluminescent dinoflagellate ecosystem bays are among the rarest and most fragile, with the most famous ones being the Bioluminescent Bay in La Parguera, Lajas
, Puerto Rico; Mosquito Bay in Vieques, Puerto Rico
; and Las Cabezas de San Juan Reserva Natural Fajardo, Puerto Rico
. Also, a bioluminescent lagoon is near Montego Bay, Jamaica, and bioluminescent harbors surround Castine, Maine. Within the United States, Central Florida is home to the Indian River Lagoon
which is abundant with dinoflagellates in the summer and bioluminescent ctenophore in the winter.
Lipid and sterol production
Dinoflagellates produce characteristic lipids and sterols. One of these sterols is typical of dinoflagellates and is called dinosterol
can sink rapidly to the seafloor in marine snow
Dinoflagellates have a haplontic life cycle
, with the possible exception of ''Noctiluca'' and its relatives.
The life cycle usually involves asexual reproduction by means of mitosis, either through desmoschisis
. More complex life cycles occur, more particularly with parasitic dinoflagellates. Sexual reproduction also occurs, though this mode of reproduction is only known in a small percentage of dinoflagellates. This takes place by fusion of two individuals to form a zygote
, which may remain mobile in typical dinoflagellate fashion and is then called a planozygote. This zygote may later form a resting stage or hypnozygote
, which is called a dinoflagellate cyst
. After (or before) germination of the cyst, the hatchling undergoes meiosis
to produce new haploid cell
s. Dinoflagellates appear to be capable of carrying out several DNA repair
processes that can deal with different types of DNA damage
One of their most striking features is the large amount of cellular DNA that dinoflagellates contain. Most eukaryotic algae contain on average about 0.54 pg DNA/cell, whereas estimates of dinoflagellate DNA content range from 3–250 pg/cell,
corresponding to roughly 3000–215 000 Mb (in comparison, the haploid human genome is 3180 Mb and hexaploid ''Triticum'' wheat is 16 000 Mb). Polyploidy
or polyteny may account for this large cellular DNA content, but earlier studies of DNA reassociation kinetics and recent genome analyses do not support this hypothesis. Rather, this has been attributed, hypothetically, to the rampant retroposition found in dinoflagellate genomes.
In addition to their disproportionately large genomes, dinoflagellate nuclei are unique in their morphology, regulation, and composition. Their DNA is so tightly packed it is still uncertain exactly how many chromosomes they have.
The dinoflagellates share an unusual mitochondrial genome organisation with their relatives, the Apicomplexa
Both groups have very reduced mitochondrial genomes (around 6 kilobases (kb) in the Apicomplexa vs ~16kb for human mitochondria). One species, ''Amoebophrya ceratii'', has lost its mitochondrial genome completely, yet still has functional mitochondria. The genes on the dinoflagellate genomes have undergone a number of reorganisations, including massive genome amplification and recombination which have resulted in multiple copies of each gene and gene fragments linked in numerous combinations. Loss of the standard stop codons, trans-splicing of mRNAs for the mRNA of cox3, and extensive RNA editing recoding of most genes has occurred. The reasons for this transformation are unknown. In a small group of dinoflagellates, called ‘dinotoms’ (Durinskia
and Kryptoperidinium), the endosymbionts (diatoms) still have mitochondria, making them the only organisms with two evolutionarily distinct mitochondria.
In most of the species, the plastid genome consist of just 14 genes.
The DNA of the plastid in the peridinin-containing dinoflagellates is contained in a series of small circles.
Each circle contains one or two polypeptide genes. The genes for these polypeptides are chloroplast-specific because their homologs from other photosynthetic eukaryotes are exclusively encoded in the chloroplast genome. Within each circle is a distinguishable 'core' region. Genes are always in the same orientation with respect to this core region.
In terms of DNA barcoding
, ITS sequences can be used to identify species, where a genetic distance of p≥0.04 can be used to delimit species, which has been successfully applied to resolve long-standing taxonomic confusion as in the case of resolving the Alexandrium tamarense complex into five species. A recent study revealed a substantial proportion of dinoflagellate genes encode for unknown functions, and that these genes could be conserved and lineage-specific.
Dinoflagellates are mainly represented as fossils by fossil dinocysts
, which have a long geological record with lowest occurrences during the mid-Triassic
, whilst geochemical markers suggest a presence to the Early Cambrian.
Some evidence indicates dinosteroids in many Paleozoic
rocks might be the product of ancestral dinoflagellates (protodinoflagellates).
Molecular phylogenetics show that dinoflagellates are grouped with ciliates
(=Sporozoa) in a well-supported clade, the alveolates
. The closest relatives to dinokaryotic dinoflagellates appear to be apicomplexans
, ''Perkinsus, Parvilucifera'', syndinians, and ''Oxyrrhis''. Molecular phylogenies are similar to phylogenies based on morphology.
The earliest stages of dinoflagellate evolution appear to be dominated by parasitic lineages, such as perkinsids and syndinians (e.g. ''Amoebophrya'' and ''Hematodinium'').
All dinoflagellates contain red algal plastids or remnant (nonphotosynthetic) organelles of red algal origin. The parasitic dinoflagellate ''Hematodinium'' however lacks a plastid entirely. Some groups that have lost the photosynthetic properties of their original red algae plastids has obtained new photosynthetic plastids (chloroplasts) through so-called serial endosymbiosis, both secondary and tertiary. Like their original plastids, the new chloroplasts in these groups can be traced back to red algae, except from those in the members of the genus Lepidodinium, which possess plastids derived from green algae, possibly Trebouxiophyceae
. Lineages with tertiary endosymbiosis are Dinophysis, with plastids from a cryptomonad
, the Karenia, Karlodinium, and Takayama, which possess plastids of haptophyte
origin, and the Peridiniaceae, Durinskia and Kryptoperidinium, which has plastids derived from diatom
s Some species also perform kleptoplasty
Dinoflagellate evolution has been summarized into five principal organizational types: prorocentroid, dinophysoid, gonyaulacoid, peridinioid, and gymnodinoid.
The transitions of marine species into fresh water have been infrequent events during the diversification of dinoflagellates and in most cases have not occurred recently, possibly as late as the Cretaceous
Recently, the "living fossil" ''Dapsilidinium pastielsii'' was found inhabiting the Indo-Pacific Warm Pool
, which served as a refugium
for thermophilic dinoflagellates.
* ''Lingulodinium polyedrum
Image:Oxyrrhis marina.jpg|''Oxyrrhis marina'' (Oxyrrhea)
Dinophysis acuminata.jpg|''Dinophysis acuminata'' (Dinophyceae)
Image:Ceratium sp umitunoobimusi.jpg|''Ceratium macroceros'' (Dinophyceae)
Image:Ceratium furca.jpg|''Ceratium furcoides'' (Dinophyceae)
File:Dinoflagellate - SEM MUSE.tif|Unknown dinoflagellate under SEM (Dinophyceae)
Image:Pfiesteria shumwayae.jpg|''Pfiesteria shumwayae'' (Dinophyceae)
File:Symbiodinium.png|''Symbiodinium'' sp. (Dinophyceae): zooxanthella, a coral endosymbiont
Image:Noctiluca scintillans varias.jpg|''Noctiluca scintillans'' (Noctiluciphyceae)
* Paralytic shellfish poisoning
*Thin layers (oceanography)
International Society for the Study of Harmful AlgaeClassic dinoflagellate monographs ttps://web.archive.org/web/20080930064242/http://www.tafi.org.au/ Tasmanian Aquaculture & Fisheries Institute
br>Tree of Life DinoflagellatesCentre of Excellence for Dinophyte Taxonomy CEDiTDinoflagellates
Category:Olenekian first appearances
Category:Extant Early Triassic first appearances