Ceratocorys is a genus of photosynthetic free-living marine dinoflagellates first described in 1883 by Friedrich Stein. Currently consisting of 12 species, this genus is typically found at the water surface in tropical and subtropical ocean regions, and has both low nutrient requirements and salinity sensitivity. All species in the genus have a theca; 29 membrane-bound armored plates with anywhere from 2 to 6 spines protruding from the cell. They reproduce through binary fission at temperatures above 20 °C during asexual reproduction and whether or not they have sexual reproduction is not known. Due to its bioluminescent capabilities, the type species of this genus, Ceratocorys horrida, has many practical applications. Its bioluminescent response to water flow means it can act as a model organism for understanding planktonic reaction to water movement. It is also sensitive to environmental molecules; by measuring the bioluminescent response it can be used in rapid toxicity tests to detect the levels of different contaminants in water systems. Its presence is also an indicator of different oceanic phenomena like upwellings or tropical waters.
Etymology Etymology not provided in the original description.
Type species Ceratocorys horrida
History The type species of Ceratocorys (C. horrida) was first described by Friedrich Stein in 1883 in the third volume of Der Organismus der Infusionsthiere.Stein, F. (1859). Der Organismus der Infusionsthiere (pp. 1–404). W. Engelmann. The specimens were found in the Kvarner Gulf in Croatia, part of the Pacific Ocean. The next species to be described, currently accepted as C. bipes, was first described in 1903 by P. T. Cleves as Goniodoma bipes but was then renamed to its currently taxonomically accepted name by C. A. Kofoid in 1910. In the same year, C. A. Kofoid also described C. armata (previously known as Goniodoma acuminatum var. armata, described by F. Schütt in 1895Schütt, F. (1895). Die Peridineen der Plankton-Expedition. Ergebnisse der Plankton-Expedition der Humboldt-Stiftung 4: 1-170) and C. magna.Kofoid, C.A. (1910). A revision of the genus Ceratocorys based on skeletal morphology. University of California Publications in Zoology 6(8): 177-187. O. Paulsen described C. kofoidii in 1931 and C. gourretii in 1937. In 1941, H. W. Graham described three species: C. aultii, C. reticulata, and C. skogsbergii.Graham, H. W., 1905. (1942). Studies in the morphology, taxonomy, and ecology of the peridiniales. Carnegie Institution, 1942. C. indica was described by E. J. F. Wood in 1963. C. acantha and C. grahamii were described by M. C. Carbonell-Moore in 1996. All of this information was summarized by F. Gomez in 2005 in "A list of free-living dinoflagellates in the world's oceans".Gomez, F. (2005). A list of free-living dinoflagellate species in the world's oceans. Acta Botanica Croatica, 64(1), 129-212. The most recently taxonomically accepted described species in this genus is C. malayensis, described by Z. Luo, P. T. Lim, and H. Gu in 2019.
Many "new species" of Ceratocorys described throughout history have simply been a mislabelling of daughter cells of known species that had not yet fully developed their horns (reproduction will be elaborated on in the organismal description section). As an example, Matzenauer in 1933 described a "new species" of Ceratocorys that he called C. hirsuta, but the figures drawn very closely resembled a C. horrida cell lacking two of its spines.
Habitat and ecology The organisms in this genus are all marine species and live in tropical and subtropical ocean regions. Like other dinoflagellates, this genus favours intermediate salinity,.Ilangovan, G. (1987). A comparative study on species diversity, distribution and ecology of the Dinophyceae from Vellar Estuary and nearby Bay of Bengal. Journal of the Marine Biological Association of India, 29(1-2), 280-285. though organisms within it are found in such a wide range of salinities that this genus likely has low sensitivity to salinity levels. They are also considered oligotrophic organisms with low nutrient requirements, having been found in regions where the phosphate content of the water was <10 mg/m3. While most dinoflagellates are mixotrophic, so far it seems that Ceratocorys are autotrophic. Since these organisms are photosynthetic and require sunlight to make food, they are most often found at the surface of the water
The type species C. horrida is very widespread, having been found in the Atlantic, Pacific, Mediterranean, Indian, Red, and Arabian Oceans. It is found in both hemispheres nearly entirely year-round. The distribution limits of this species are sharply marked by the 19 °C isotherm, rarely ever appearing where the surface temperature is below 19 °C (Fig. 52C).
C. armata likely has a similar range to that of C. horrida, though is slightly more limited to warm water, and is also rarer (Fig. 52B).
C. reticulata is a distinctly tropical species and is even more limited to higher temperatures than C. horrida or C. armata (Fig. 52A).
C. aultii is also a tropical species but is rare and has a sparse population. It has not been found anywhere where the water surface temperature is below 19 °C and it is also possible that, unlike the other species in this genus that live near the surface of the water, it may be more abundant below 100m (Fig. 52A).
C. bipes, like C. aultii, is a rare tropical species, and is much more restricted to warm tropical water than any other species in the genus, having never been found at any area where the surface temperature was lower than 20 °C (Fig. 52A).
C. gourretii is a widespread but rare tropical species, even more restricted to warm waters than C. bipes and having never been found anywhere with surface temperature lower than 22.3 °C (Fig. 52B).
C. skogsbergii is found in the southwestern Pacific, but is such a rare tropical species that no significant distributional correlation can be made (Fig. 52B).
Wood describes C. indica as being distributed in the East Indian Ocean. When first described, C. acantha was found in the Caribbean Sea.
C. malayensis has been found in Malaysian waters.
Due to the nearly ubiquitous presence of Ceratocorys in the oceans, it is ecologically important as a primary producer, though what organisms it specifically interacts with is not well known. As a fully autotrophic organism it does not prey on any other species and is instead preyed on by heterotrophic organisms. It is also hypothesized that the bioluminescent capability of C. horrida is a defense mechanism against predation, acting either to startle the predator from feeding or to alert an even higher-level predator of its presence.
Description
Ceratocorys, as a genus of dinoflagellate eukaryotic autotrophic organisms, contains all the organelles one would expect to find; a dinokaryon, smooth and rough endoplasmic reticulum, vacuoles, chloroplasts, and golgi bodies, as well as other specialized organelles.Postgraduate Unit of Micropalaeontology, U. C. L. (2002). Dinoflagellates and Dinocysts (micropalaeontology Proterozoic (Pre-Cambrian) to Recent) [Text, image]. Various; Postgraduate Unit of Micropalaeontology, Department of Earth Sciences, University College London, Gower Street, London, WC1E 6BT. https://www.ucl.ac.uk/GeolSci/micropal/dinoflagellate.html
Bioluminescence Many dinoflagellates are bioluminescent, and Ceratocorys is no exception, emitting a blue-green light. Dinoflagellates are also the only known photosynthetic organisms with bioluminescent capabilities. The gene responsible for this bioluminescence in dinoflagellates is known as the dinoflagellate luciferase gene (lcf). C. horrida produces bioluminescence when exposed to shear stress in water, caused by things such as waves or wind at the water surface.Rosen, G., Osorio-Robayo, A., Rivera-Duarte, I., & Lapota, D. (2008). Comparison of bioluminescent dinoflagellate (QwikLite) and bacterial (microtox) rapid bioassays for the detection of metal and ammonia toxicity. Archives of Environmental Contamination and Toxicology, 54(4), 606-611. The light is produced in specialized organelles known as scintillions which contain both the substrate luciferin and the enzyme luciferase. When the cell is agitated, a series of reactions leads to a decrease in pH in the scintillion organelles, changing the luciferase conformation and allowing it to bind to luciferin, which causes the flash of light.
Morphology There is quite some variation of size and shape between species in this genus. Cell length varies from 38μm in C. gourretti to 99μm in C. armata. Measurements in C. horrida are 38-97μm lengthwise and a diameter of 43-92μm at the girdle. Cell girdle width for these same species varies from 28μm to 114μm respectively. All members of this genus are angular in shape with the exception of C. gouretti, with C. horrida being the most angular. Girdle placement also varies between species; it is almost equatorialin C. armata and C. reticulata and is more anteriorly positioned in other species, furthest anterior in C. horrida and C. gouretti.
Thecal plate patterning of the Ceratocorys genus is extremely consistent between species. There is a total of 29 plates; 10 epithecal plates (5 apical plates, 5 postcingular plates), 6 girdle plates, 5 ventral sulcal plates, 8 hypothecal plates (6 postcingular plates, 1 antapical plate, and 1 posterior intercalary plate).
The anterior apical pore is covered by an apical closing platelet not attached to any other plate. A total of 4 plates are in the apical region but only 2 touch the apical closing platelet are considered apical plates. These are called the first and second apical plates, which surround the left-dorsal and right-ventral edges of the pore respectively. The other two are called the first and second anterior intercalary plates, the first of which is a small square plate between the first and second apical plates, and the second of which bears the ventral epithecal pore (Fig. 44B).
The 5 postcingular plates surround the 5 apical plates and are counted one through five counterclockwise from the bottom right. The fifth plate is smaller than the first four posterior to second anterior intercalary and second apical plates (Fig. 44B).
The 6 girdle plates are of approximately equal length (Fig. 44A).
5 sulcal plates make up the ventral area surrounding the flagellar pore. The smallest of the sulcal plates of the cell is the rectangular posterior sulcal plate. Anterior to this is the left sulcal plate that forms the posterior edge of the flagellar pore. On the right of the ventral area there are two plates between the anterior and posterior called the right and right accessory sulcal plates. Along with the last of the five sulcal plates known as the anterior sulcal plate, the right accessory plate makes up the anterior edge of the flagellar pore. Only in C. gouretti and C. skogsbergii is there a sixth sulcal plate known as the left accessory sulcal plate, which is analogous to postcingular plate 1 in all other Ceratocorys species (Fig. 44A, 47B).
There are 6 postcingular plates in the Ceratocorys genus. All members of the genus with the exception of C. gouretti and C. skogsbergii have 6 plates; these two species only have plates two through six, as plate one has become the left accessory sulcal plate. Postcingular plates one and two are small and separated from plate three by a list, whereas plates three through six are large and, along with the antapical plate, make up the main body of the hypotheca. The last two plates that make up the theca of Ceratocorys cells is the posterior intercalary plate. The posterior intercalary plate is between the postcingular plates 1-2 and the antapical plate on the left of the sulcus (Fig. 44A).