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Paramecium

Paramecium (/ˌpærəˈmʃ(i)əm/ PARR-ə-MEE-sh(ee-)əm, /-siəm/ -⁠see-əm; also spelled Paramoecium)[1] is a genus of eukaryotic, unicellular ciliates, commonly studied as a representative of the ciliate group. Paramecia are widespread in freshwater, brackish, and marine environments and are often very abundant in stagnant basins and ponds. Because some species are readily cultivated and easily induced to conjugate and divide, it has been widely used in classrooms and laboratories to study biological processes. Its usefulness as a model organism has caused one ciliate researcher to characterize it as the "white rat" of the phylum Ciliophora.[2]

Paramecium
Paramecium aurelia
Scientific classification
Kingdom: Chromista
Superphylum: Alveolata
Phylum: Ciliophora
Class: Oligohymenophorea
Order: Peniculida
Family: Parameciidae
Genus: Paramecium
Müller, 1773
Species

See text

Synonyms
  • Paramoecium
  • Paramœcium
  • Paramecia

Historical background

 
Paramecia, illustrated by Otto Müller, 1773
 
Earliest known illustration of Paramecium
 
"Slipper animalcule", illustrated by Louis Joblot, 1718

Paramecia were among the first ciliates to be seen by microscopists, in the late 17th century. They were probably known to the Dutch pioneer of protozoology, Antonie van Leeuwenhoek, and were clearly described by his contemporary Christiaan Huygens in a letter of 1678.[3] The earliest known illustration of a Paramecium was published anonymously in Philosophical Transactions of the Royal Society, in 1703.[4]

In 1718, the French mathematics teacher and microscopist Louis Joblot published a description and illustration of a microscopic poisson (fish), which he discovered in an infusion of oak bark in water. Joblot gave this creature the name "Chausson", or "slipper", and the phrase "slipper animalcule" remained in use as a colloquial epithet for Paramecium, throughout the 18th and 19th centuries.[5]

The name "Paramecium" – constructed from the Greek παραμήκης (paramēkēs, "oblong") – was coined in 1752 by the English microscopist John Hill, who applied the name generally to "Animalcules which have no visible limbs or tails, and are of an irregularly oblong figure".[6] In 1773, O. F. Müller, the first researcher to place the genus within the Linnaean system of taxonomy, adopted the name Paramecium, but changed the spelling to Paramœcium. C. G. Ehrenberg, in a major study of the infusoria published in 1838, restored Hill's original spelling for the genus name, and most researchers have followed his lead.[7]

Description

 

Species of Paramecium range in size from 50 to 330 micrometres (0.0020 to 0.0130 in) in length. Cells are typically ovoid, elongate, foot- or cigar-shaped.

The body of the cell is enclosed by a stiff but elastic structure called the pellicle. This consists of the outer cell membrane (plasma membrane), a layer of flattened membrane-bound sacs called alveoli, and an inner membrane called the epiplasm. The pellicle is not smooth, but textured with hexagonal or rectangular depressions. Each of these polygons is perforated by a central aperture through which a single cilium projects. Between the alveolar sacs of the pellicle, most species of Paramecium have closely spaced spindle-shaped trichocysts, explosive organelles that discharge thin, non-toxic filaments, often used for defensive purposes.[8][9]

Typically, an anal pore (cytoproct) is located on the ventral surface, in the posterior half of the cell. In all species, there is a deep oral groove running from the anterior of the cell to its midpoint. This is lined with inconspicuous cilia which beat continuously, drawing food inside the cell.[10] Paramecia live mainly by heterotrophy, feeding on bacteria and other small organisms. A few species are mixotrophs, deriving some nutrients from endosymbiotic algae (chlorella) carried in the cytoplasm of the cell.[11]

Osmoregulation is carried out by contractile vacuoles, which actively expel water from the cell to compensate for fluid absorbed by osmosis from its surroundings.[12] The number of contractile vacuoles varies from one, to many, depending on species.[10]

Movement

A Paramecium propels itself by whiplash movements of the cilia, which are arranged in tightly spaced rows around the outside of the body. The beat of each cilium has two phases: a fast "effective stroke", during which the cilium is relatively stiff, followed by a slow "recovery stroke", during which the cilium curls loosely to one side and sweeps forward in a counter-clockwise fashion. The densely arrayed cilia move in a coordinated fashion, with waves of activity moving across the "ciliary carpet", creating an effect sometimes likened to that of the wind blowing across a field of grain.[13]

The Paramecium spirals through the water as it progresses. When it happens to encounter an obstacle, the "effective stroke" of its cilia is reversed and the organism swims backward for a brief time, before resuming its forward progress. This is called the avoidance reaction. If it runs into the solid object again, it repeats this process, until it can get past the object.[14]

It has been calculated that a Paramecium expends more than half of its energy in propelling itself through the water.[15] This ciliary method of locomotion has been found to be less than 1% efficient. This low percentage is nevertheless close to the maximum theoretical efficiency that can be achieved by an organism equipped with cilia as short as those of the members of Paramecium.[16]

Gathering food

 
Paramecium feeding on Bacteria

Paramecia feed on microorganisms like bacteria, algae, and yeasts. To gather food, the Paramecium makes movements with cilia to sweep prey organisms, along with some water, through the oral groove (vestibulum, or vestibule), and into the cell. The food passes from the cilia-lined oral groove into a narrower structure known as the buccal cavity (gullet). From there, food particles pass through a small opening called the cytostome, or cell mouth, and move into the interior of the cell. As food enters the cell, it is gathered into food vacuoles, which are periodically closed off and released into the cytoplasm, where they begin circulating through the cell body by the streaming movement of the cell contents, a process called cyclosis or cytoplasmic streaming. As a food vacuole moves along, enzymes from the cytoplasm enter it, to digest the contents. As enzymatic digestion proceeds, the vacuole contents become more acidic. Within five minutes of a vacuole's formation, pH of its contents drops from 7 to 3.[17] As digested nutrients pass into the cytoplasm, the vacuole shrinks. When the vacuole, with its fully digested contents, reaches the anal pore, it ruptures, expelling its waste contents to the environment, outside the cell.[18][19][20]

Symbiosis

Some species of Paramecium form mutualistic relationships with other organisms. Paramecium bursaria and Paramecium chlorelligerum harbour endosymbiotic green algae, from which they derive nutrients and a degree of protection from predators such as Didinium nasutum.[21][22] Numerous bacterial endosymbionts have been identified in species of Paramecium.[23] Some intracellular bacteria, known as Kappa particles, giving Paramecia the ability to kill other strains of Paramecium that lack Kappa particles.[23]

Genome

The genome of the species Paramecium tetraurelia has been sequenced, providing evidence for three whole-genome duplications.[24]

In some ciliates, like Stylonychia and Paramecium, only UGA is decoded as a stop codon, while UAG and UAA are reassigned as sense codons (that is, codons that code for standard amino acids), coding for the amino acid glutamic acid.[25]

Learning

The question of whether Paramecia exhibit learning has been the object of a great deal of experimentation, yielding equivocal results. However, a study published in 2006 seems to show that Paramecium caudatum may be trained, through the application of a 6.5 volt electric current, to discriminate between brightness levels.[26] This experiment has been cited as a possible instance of cell memory, or epigenetic learning in organisms with no nervous system.[27]

Reproduction and sexual phenomena

Reproduction

Like all ciliates, Paramecium has a dual nuclear apparatus, consisting of a polyploid macronucleus, and one or more diploid micronuclei. The macronucleus controls non-reproductive cell functions, expressing the genes needed for daily functioning. The micronucleus is the generative, or germline nucleus, containing the genetic material that is passed along from one generation to the next.[28]

Paramecium reproduction is asexual, by binary fission, which has been characterized as "the sole mode of reproduction in ciliates" (conjugation being a sexual phenomenon, not directly resulting in increase of numbers).[2][29] During fission, the macronucleus splits by a type of amitosis, and the micronuclei undergo mitosis. The cell then divides transversally, and each new cell obtains a copy of the micronucleus and the macronucleus.[2]

Fission may occur spontaneously, in the course of the vegetative cell cycle. Under certain conditions, it may be preceded by self-fertilization (autogamy),[30] or it may immediately follow conjugation, in which Paramecia of compatible mating types fuse temporarily and exchange genetic material.

Conjugation

In ciliates such as Paramecium, conjugation is a sexual phenomenon that results in genetic recombination and nuclear reorganization within the cell.[28][23] During conjugation, two Paramecia of a compatible mating type come together and a bridge forms between their cytoplasms. Their respective micronuclei undergo meiosis, and haploid micronuclei are exchanged over the bridge. Following conjugation, the cells separate. The old macronuclei are destroyed, and both post-conjugants form new macronuclei, by amplification of DNA in their micronuclei.[28] Conjugation is followed by one or more "exconjugant divisions".[31]

Stages of conjugation
 
Stages of conjugation in Paramecium caudatum

In Paramecium caudatum, the stages of conjugation are as follows (see diagram at right):

  1. Compatible mating strains meet and partly fuse
  2. The micronuclei undergo meiosis, producing four haploid micronuclei per cell.
  3. Three of these micronuclei disintegrate. The fourth undergoes mitosis.
  4. The two cells exchange a micronucleus.
  5. The cells then separate.
  6. The micronuclei in each cell fuse, forming a diploid micronucleus.
  7. Mitosis occurs three times, giving rise to eight micronuclei.
  8. Four of the new micronuclei transform into macronuclei, and the old macronucleus disintegrates.
  9. Binary fission occurs twice, yielding four identical daughter cells.

Aging

In the asexual fission phase of growth, during which cell divisions occur by mitosis rather than meiosis, clonal aging occurs leading to a gradual loss of vitality. In some species, such as the well studied Paramecium tetraurelia, the asexual line of clonally aging Paramecia loses vitality and expires after about 200 fissions if the cells fail to undergo autogamy or conjugation. The basis for clonal aging was clarified by transplantation experiments of Aufderheide in 1986.[32] When macronuclei of clonally young Paramecia were injected into Paramecia of standard clonal age, the lifespan (clonal fissions) of the recipient was prolonged. In contrast, transfer of cytoplasm from clonally young Paramecia did not prolong the lifespan of the recipient. These experiments indicated that the macronucleus, rather than the cytoplasm, is responsible for clonal aging. Other experiments by Smith-Sonneborn,[33] Holmes and Holmes,[34] and Gilley and Blackburn[35] demonstrated that, during clonal aging, DNA damage increases dramatically.[36] Thus, DNA damage in the macronucleus appears to be the cause of aging in P. tetraurelia. In this single-celled protist, aging appears to proceed as it does in multicellular eukaryotes, as described in DNA damage theory of aging.

Meiosis and rejuvenation

When clonally aged P. tetraurelia are stimulated to undergo meiosis in association with either conjugation or automixis, the genetic descendants are rejuvenated, and are able to have many more mitotic binary fission divisions. During either of these processes, the micronuclei of the cell(s) undergo meiosis, the old macronucleus disintegrates and a new macronucleus is formed by replication of the micronuclear DNA that had recently undergone meiosis. There is apparently little, if any, DNA damage in the new macronucleus. These findings further solidify that clonal aging is due, in large part, to a progressive accumulation of DNA damage; and that rejuvenation is due to the repair of this damage in the micronucleus during meiosis. Meiosis appears to be an adaptation for DNA repair and rejuvenation in P. tetraurelia.[37] In P. tetraurelia, CtlP protein is a key factor needed for the completion of meiosis during sexual reproduction and recovery of viable sexual progeny.[37] The CtlP and Mre11 nuclease complex are essential for accurate processing and repair of double-strand breaks during homologous recombination.[37]

Video gallery

List of species

Paramecium aurelia species complex:

  • Paramecium primaurelia
  • Paramecium biaurelia
  • Paramecium triaurelia
  • Paramecium tetraurelia
  • Paramecium pentaurelia
  • Paramecium sexaurelia
  • Paramecium septaurelia
  • Paramecium octaurelia
  • Paramecium novaurelia
  • Paramecium decaurelia
  • Paramecium undecaurelia
  • Paramecium dodecaurelia
  • Paramecium tredecaurelia
  • Paramecium quadecaurelia
  • Paramecium sonneborni

Other species:

  • Paramecium buetschlii
  • Paramecium bursaria
  • Paramecium calkinsi
  • Paramecium caudatum
  • Paramecium chlorelligerum
  • Paramecium duboscqui
  • Paramecium grohmannae
  • Paramecium jenningsi
  • Paramecium multimicronucleatum
  • Paramecium nephridiatum
  • Paramecium polycaryum
  • Paramecium putrinum
  • Paramecium schewiakoffi
  • Paramecium woodruffi

References

  1. ^ "paramecium". Merriam-Webster Dictionary.
  2. ^ a b c Lynn, Denis (2008). The Ciliated Protozoa: Characterization, Classification, and Guide to the Literature. Springer Science & Business Media. p. 30. ISBN 9781402082399.
  3. ^ Dobell, Clifford (1932). Antony van Leeuwenhoek and his "Little Animals" (1960 ed.). New York: Dover. pp. 164–165. ISBN 978-0-486-60594-4.
  4. ^ Dolan, John R. (2019-08-01). "Unmasking "The Eldest Son of The Father of Protozoology": Charles King". Protist. 170 (4): 374–384. doi:10.1016/j.protis.2019.07.002. ISSN 1434-4610. PMID 31479910.
  5. ^ Joblot, Louis (1718). Description et usages de Plusieurs Nouveaux Microscopes, tant simple que composez (in French). Vol. 2. Paris: Jacques Collombat. p. 79.
  6. ^ Hill, John (1752). An History of Animals. Paris: Thomas Osborne. p. 5.
  7. ^ Woodruff, Lorande Loss (September 1921). "The structure, life history, and intrageneric relationships of Paramecium calkinsi, sp. nov". The Biological Bulletin. 41 (3): 171–180. doi:10.2307/1536748. JSTOR 1536748.
  8. ^ Lynn, Denis (2008). The Ciliated Protozoa: Characterization, Classification, and Guide to the Literature (3 ed.). Springer Netherlands. ISBN 9781402082382.
  9. ^ Wichterman, R. (2012-12-06). The Biology of Paramecium. Springer Science & Business Media. ISBN 9781475703726.
  10. ^ a b Curds, Colin R.; Gates, Michael; Roberts, David McL. (1983). British and other freshwater ciliated protozoa. Vol. 2. Cambridge University Press. p. 126.
  11. ^ Esteban, Genoveva F.; Fenchel, Tom; Finlay, Bland J. (2010). "Mixotrophy in Ciliates". Protist. 161 (5): 621–641. doi:10.1016/j.protis.2010.08.002. PMID 20970377.
  12. ^ Reece, Jane B. (2011). Campbell Biology. San Francisco: Pearson Education. p. 134. ISBN 9780321558237.
  13. ^ Blake, John R.; Sleigh, Michael A. (February 1974). "Mechanics of ciliary locomotion". Biological Reviews. 49 (1): 85–125. doi:10.1111/j.1469-185x.1974.tb01299.x. PMID 4206625. S2CID 41907168.
  14. ^ Ogura, A., and K. Takahashi. "Artificial deciliation causes loss of calcium-dependent responses in Paramecium" (1976): 170–172.
  15. ^ Katsu-Kimura, Yumiko; et al. (2009). "Substantial energy expenditure for locomotion in ciliates verified by means of simultaneous measurement of oxygen consumption rate and swimming speed". Journal of Experimental Biology. 212 (12): 1819–1824. doi:10.1242/jeb.028894. PMID 19482999.
  16. ^ Osterman, Natan; Vilfan, Andrej (September 20, 2011). "Finding the ciliary beating pattern with optimal efficiency" (PDF). Proceedings of the National Academy of Sciences. 108 (38): 15727–15732. arXiv:1107.4273. Bibcode:2011PNAS..10815727O. doi:10.1073/pnas.1107889108. PMC 3179098. PMID 21896741.
  17. ^ Wichterman, R. (1986). The Biology of Paramecium. Springer US. pp. 200–1. ISBN 9781475703740.
  18. ^ Wichterman, Ralph (1985). The Biology of Paramecium. New York: Plenum Press. pp. 88–90. ISBN 978-1-4757-0374-0.
  19. ^ Reece, Jane B.; et al. (2011). Campbell Biology. San Francisco: Pearson Education. p. 584. ISBN 9780321558237.
  20. ^ Mast, S. O. (February 1947). "The food-vacuole in Paramecium". The Biological Bulletin. 92 (1): 31–72. doi:10.2307/1537967. JSTOR 1537967. PMID 20284992.
  21. ^ Berger, Jacques (1980). "Feeding Behaviour of Didinium nasutum on Paramecium bursaria with Normal or Apochlorotic Zoochlorellae". Journal of General Microbiology. 118 (2): 397–404. doi:10.1099/00221287-118-2-397.
  22. ^ Kreutz, Martin; Stoeck, Thorsten; Foissner, Wilhelm (2012). "Morphological and Molecular Characterization of Paramecium (Viridoparamecium nov. subgen.) chlorelligerum Kahl (Ciliophora)". Journal of Eukaryotic Microbiology. 59 (6): 548–563. doi:10.1111/j.1550-7408.2012.00638.x. PMC 3866650. PMID 22827482.
  23. ^ a b c Preer, John R. Jr.; Preer, Louise B.; Jurand, Artur (June 1974). "Kappa and Other Endosymbionts in Paramecium aurelia". Bacteriological Reviews. 38 (2): 113–163. doi:10.1128/MMBR.38.2.113-163.1974. PMC 413848. PMID 4599970.
  24. ^ Aury, Jean-Marc; Jaillon, Oliver; Wincker, Patrick; et al. (November 2006). "Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia". Nature. 444 (7116): 171–8. Bibcode:2006Natur.444..171A. doi:10.1038/nature05230. PMID 17086204.
  25. ^ Lekomtsev, Sergey; Kolosov, Petr; Bidou, Laure; Frolova, Ludmila; Rousset, Jean-Pierre; Kisselev, Lev (June 26, 2007). "Different modes of stop codon restriction by the Stylonychia and Paramecium eRF1 translation termination factors". Proceedings of the National Academy of Sciences of the United States of America. 104 (26): 10824–9. Bibcode:2007PNAS..10410824L. doi:10.1073/pnas.0703887104. PMC 1904165. PMID 17573528.
  26. ^ Armus, Harvard L.; Montgomery, Amber R.; Jellison, Jenny L. (Fall 2006). "Discrimination Learning in Paramecia (P. caudatum)". The Psychological Record. 56 (4): 489–498. doi:10.1007/BF03396029. S2CID 142785414.
  27. ^ Ginsburg, Simona; Jablonka, Eva (2009). "Epigenetic learning in non-neural organisms". Journal of Biosciences. 34 (4): 633–646. doi:10.1007/s12038-009-0081-8. PMID 19920348. S2CID 15507569.
  28. ^ a b c Prescott, D. M.; et al. (1971). "DNA of ciliated protozoa". Chromosoma. 34 (4): 355–366. doi:10.1007/bf00326311. S2CID 5013543.
  29. ^ Raikov, I.B (1972). "Nuclear phenomena during conjugation and autogamy in ciliates". Research in Protozoology. 4: 149.
  30. ^ Berger, James D. (October 1986). "Autogamy in Paramecium cell cycle stage-specific commitment to meiosis". Experimental Cell Research. 166 (2): 475–485. doi:10.1016/0014-4827(86)90492-1. PMID 3743667.
  31. ^ Raikov, I.B (1972). "Nuclear phenomena during conjugation and autogamy in ciliates". Research in Protozoology. 4: 151, 240.
  32. ^ Aufderheide, Karl J. (1986). "Clonal aging in Paramecium tetraurelia. II. Evidence of functional changes in the macronucleus with age". Mechanisms of Ageing and Development. 37 (3): 265–279. doi:10.1016/0047-6374(86)90044-8. PMID 3553762. S2CID 28320562.
  33. ^ Smith-Sonneborn, J. (1979). "DNA repair and longevity assurance in Paramecium tetraurelia". Science. 203 (4385): 1115–1117. Bibcode:1979Sci...203.1115S. doi:10.1126/science.424739. PMID 424739.
  34. ^ Holmes, George E.; Holmes, Norreen R. (July 1986). "Accumulation of DNA damages in aging Paramecium tetraurelia". Molecular and General Genetics. 204 (1): 108–114. doi:10.1007/bf00330196. PMID 3091993. S2CID 11992591.
  35. ^ Gilley, David; Blackburn, Elizabeth H. (1994). "Lack of telomere shortening during senescence in Paramecium" (PDF). Proceedings of the National Academy of Sciences of the United States of America. 91 (5): 1955–1958. Bibcode:1994PNAS...91.1955G. doi:10.1073/pnas.91.5.1955. PMC 43283. PMID 8127914.
  36. ^ Bernstein, H; Bernstein, C (1991). Aging, Sex, and DNA Repair. San Diego: Academic Press. pp. 153–156. ISBN 978-0120928606.
  37. ^ a b c Godau, Julia; Ferretti, Lorenza P.; Trenner, Anika; Dubois, Emeline; von Aesch, Christine; Marmignon, Antoine; Simon, Lauriane; Kapusta, Aurélie; Guérois, Raphaël; Bétermier, Mireille; Sartori, Alessandro A. (2019). "Identification of a miniature Sae2/Ctp1/CtIP ortholog from Paramecium tetraurelia required for sexual reproduction and DNA double-strand break repair" (PDF). DNA Repair. 77: 96–108. doi:10.1016/j.dnarep.2019.03.011. PMID 30928893. S2CID 89619084.

External links

  •   Media related to Paramecium at Wikimedia Commons
  •   Data related to Paramecium at Wikispecies

paramecium, paramecia, redirects, here, prehistoric, protist, paramecia, alga, parr, also, spelled, paramoecium, genus, eukaryotic, unicellular, ciliates, commonly, studied, representative, ciliate, group, paramecia, widespread, freshwater, brackish, marine, e. Paramecia redirects here For the prehistoric protist see Paramecia alga Paramecium ˌ p aer e ˈ m iː ʃ i e m PARR e MEE sh ee em s i e m see em also spelled Paramoecium 1 is a genus of eukaryotic unicellular ciliates commonly studied as a representative of the ciliate group Paramecia are widespread in freshwater brackish and marine environments and are often very abundant in stagnant basins and ponds Because some species are readily cultivated and easily induced to conjugate and divide it has been widely used in classrooms and laboratories to study biological processes Its usefulness as a model organism has caused one ciliate researcher to characterize it as the white rat of the phylum Ciliophora 2 ParameciumParamecium aureliaScientific classificationKingdom ChromistaSuperphylum AlveolataPhylum CiliophoraClass OligohymenophoreaOrder PeniculidaFamily ParameciidaeGenus ParameciumMuller 1773SpeciesSee textSynonymsParamoeciumParamœciumParamecia Contents 1 Historical background 2 Description 3 Movement 4 Gathering food 5 Symbiosis 6 Genome 7 Learning 8 Reproduction and sexual phenomena 8 1 Reproduction 8 1 1 Conjugation 9 Aging 10 Meiosis and rejuvenation 11 Video gallery 12 List of species 13 References 14 External linksHistorical background Edit Paramecia illustrated by Otto Muller 1773 Earliest known illustration of Paramecium Slipper animalcule illustrated by Louis Joblot 1718 Paramecia were among the first ciliates to be seen by microscopists in the late 17th century They were probably known to the Dutch pioneer of protozoology Antonie van Leeuwenhoek and were clearly described by his contemporary Christiaan Huygens in a letter of 1678 3 The earliest known illustration of a Paramecium was published anonymously in Philosophical Transactions of the Royal Society in 1703 4 In 1718 the French mathematics teacher and microscopist Louis Joblot published a description and illustration of a microscopic poisson fish which he discovered in an infusion of oak bark in water Joblot gave this creature the name Chausson or slipper and the phrase slipper animalcule remained in use as a colloquial epithet for Paramecium throughout the 18th and 19th centuries 5 The name Paramecium constructed from the Greek paramhkhs paramekes oblong was coined in 1752 by the English microscopist John Hill who applied the name generally to Animalcules which have no visible limbs or tails and are of an irregularly oblong figure 6 In 1773 O F Muller the first researcher to place the genus within the Linnaean system of taxonomy adopted the name Paramecium but changed the spelling to Paramœcium C G Ehrenberg in a major study of the infusoria published in 1838 restored Hill s original spelling for the genus name and most researchers have followed his lead 7 Description Edit Species of Paramecium range in size from 50 to 330 micrometres 0 0020 to 0 0130 in in length Cells are typically ovoid elongate foot or cigar shaped The body of the cell is enclosed by a stiff but elastic structure called the pellicle This consists of the outer cell membrane plasma membrane a layer of flattened membrane bound sacs called alveoli and an inner membrane called the epiplasm The pellicle is not smooth but textured with hexagonal or rectangular depressions Each of these polygons is perforated by a central aperture through which a single cilium projects Between the alveolar sacs of the pellicle most species of Paramecium have closely spaced spindle shaped trichocysts explosive organelles that discharge thin non toxic filaments often used for defensive purposes 8 9 Typically an anal pore cytoproct is located on the ventral surface in the posterior half of the cell In all species there is a deep oral groove running from the anterior of the cell to its midpoint This is lined with inconspicuous cilia which beat continuously drawing food inside the cell 10 Paramecia live mainly by heterotrophy feeding on bacteria and other small organisms A few species are mixotrophs deriving some nutrients from endosymbiotic algae chlorella carried in the cytoplasm of the cell 11 Osmoregulation is carried out by contractile vacuoles which actively expel water from the cell to compensate for fluid absorbed by osmosis from its surroundings 12 The number of contractile vacuoles varies from one to many depending on species 10 Movement EditA Paramecium propels itself by whiplash movements of the cilia which are arranged in tightly spaced rows around the outside of the body The beat of each cilium has two phases a fast effective stroke during which the cilium is relatively stiff followed by a slow recovery stroke during which the cilium curls loosely to one side and sweeps forward in a counter clockwise fashion The densely arrayed cilia move in a coordinated fashion with waves of activity moving across the ciliary carpet creating an effect sometimes likened to that of the wind blowing across a field of grain 13 The Paramecium spirals through the water as it progresses When it happens to encounter an obstacle the effective stroke of its cilia is reversed and the organism swims backward for a brief time before resuming its forward progress This is called the avoidance reaction If it runs into the solid object again it repeats this process until it can get past the object 14 It has been calculated that a Paramecium expends more than half of its energy in propelling itself through the water 15 This ciliary method of locomotion has been found to be less than 1 efficient This low percentage is nevertheless close to the maximum theoretical efficiency that can be achieved by an organism equipped with cilia as short as those of the members of Paramecium 16 Gathering food Edit Paramecium feeding on Bacteria Paramecia feed on microorganisms like bacteria algae and yeasts To gather food the Paramecium makes movements with cilia to sweep prey organisms along with some water through the oral groove vestibulum or vestibule and into the cell The food passes from the cilia lined oral groove into a narrower structure known as the buccal cavity gullet From there food particles pass through a small opening called the cytostome or cell mouth and move into the interior of the cell As food enters the cell it is gathered into food vacuoles which are periodically closed off and released into the cytoplasm where they begin circulating through the cell body by the streaming movement of the cell contents a process called cyclosis or cytoplasmic streaming As a food vacuole moves along enzymes from the cytoplasm enter it to digest the contents As enzymatic digestion proceeds the vacuole contents become more acidic Within five minutes of a vacuole s formation pH of its contents drops from 7 to 3 17 As digested nutrients pass into the cytoplasm the vacuole shrinks When the vacuole with its fully digested contents reaches the anal pore it ruptures expelling its waste contents to the environment outside the cell 18 19 20 Symbiosis EditSome species of Paramecium form mutualistic relationships with other organisms Paramecium bursaria and Paramecium chlorelligerum harbour endosymbiotic green algae from which they derive nutrients and a degree of protection from predators such as Didinium nasutum 21 22 Numerous bacterial endosymbionts have been identified in species of Paramecium 23 Some intracellular bacteria known as Kappa particles giving Paramecia the ability to kill other strains of Paramecium that lack Kappa particles 23 Genome EditThe genome of the species Paramecium tetraurelia has been sequenced providing evidence for three whole genome duplications 24 In some ciliates like Stylonychia and Paramecium only UGA is decoded as a stop codon while UAG and UAA are reassigned as sense codons that is codons that code for standard amino acids coding for the amino acid glutamic acid 25 Learning EditThe question of whether Paramecia exhibit learning has been the object of a great deal of experimentation yielding equivocal results However a study published in 2006 seems to show that Paramecium caudatum may be trained through the application of a 6 5 volt electric current to discriminate between brightness levels 26 This experiment has been cited as a possible instance of cell memory or epigenetic learning in organisms with no nervous system 27 Reproduction and sexual phenomena EditReproduction Edit Like all ciliates Paramecium has a dual nuclear apparatus consisting of a polyploid macronucleus and one or more diploid micronuclei The macronucleus controls non reproductive cell functions expressing the genes needed for daily functioning The micronucleus is the generative or germline nucleus containing the genetic material that is passed along from one generation to the next 28 Paramecium reproduction is asexual by binary fission which has been characterized as the sole mode of reproduction in ciliates conjugation being a sexual phenomenon not directly resulting in increase of numbers 2 29 During fission the macronucleus splits by a type of amitosis and the micronuclei undergo mitosis The cell then divides transversally and each new cell obtains a copy of the micronucleus and the macronucleus 2 Fission may occur spontaneously in the course of the vegetative cell cycle Under certain conditions it may be preceded by self fertilization autogamy 30 or it may immediately follow conjugation in which Paramecia of compatible mating types fuse temporarily and exchange genetic material Conjugation Edit In ciliates such as Paramecium conjugation is a sexual phenomenon that results in genetic recombination and nuclear reorganization within the cell 28 23 During conjugation two Paramecia of a compatible mating type come together and a bridge forms between their cytoplasms Their respective micronuclei undergo meiosis and haploid micronuclei are exchanged over the bridge Following conjugation the cells separate The old macronuclei are destroyed and both post conjugants form new macronuclei by amplification of DNA in their micronuclei 28 Conjugation is followed by one or more exconjugant divisions 31 Stages of conjugation Stages of conjugation in Paramecium caudatumIn Paramecium caudatum the stages of conjugation are as follows see diagram at right Compatible mating strains meet and partly fuse The micronuclei undergo meiosis producing four haploid micronuclei per cell Three of these micronuclei disintegrate The fourth undergoes mitosis The two cells exchange a micronucleus The cells then separate The micronuclei in each cell fuse forming a diploid micronucleus Mitosis occurs three times giving rise to eight micronuclei Four of the new micronuclei transform into macronuclei and the old macronucleus disintegrates Binary fission occurs twice yielding four identical daughter cells Aging EditIn the asexual fission phase of growth during which cell divisions occur by mitosis rather than meiosis clonal aging occurs leading to a gradual loss of vitality In some species such as the well studied Paramecium tetraurelia the asexual line of clonally aging Paramecia loses vitality and expires after about 200 fissions if the cells fail to undergo autogamy or conjugation The basis for clonal aging was clarified by transplantation experiments of Aufderheide in 1986 32 When macronuclei of clonally young Paramecia were injected into Paramecia of standard clonal age the lifespan clonal fissions of the recipient was prolonged In contrast transfer of cytoplasm from clonally young Paramecia did not prolong the lifespan of the recipient These experiments indicated that the macronucleus rather than the cytoplasm is responsible for clonal aging Other experiments by Smith Sonneborn 33 Holmes and Holmes 34 and Gilley and Blackburn 35 demonstrated that during clonal aging DNA damage increases dramatically 36 Thus DNA damage in the macronucleus appears to be the cause of aging in P tetraurelia In this single celled protist aging appears to proceed as it does in multicellular eukaryotes as described in DNA damage theory of aging Meiosis and rejuvenation EditWhen clonally aged P tetraurelia are stimulated to undergo meiosis in association with either conjugation or automixis the genetic descendants are rejuvenated and are able to have many more mitotic binary fission divisions During either of these processes the micronuclei of the cell s undergo meiosis the old macronucleus disintegrates and a new macronucleus is formed by replication of the micronuclear DNA that had recently undergone meiosis There is apparently little if any DNA damage in the new macronucleus These findings further solidify that clonal aging is due in large part to a progressive accumulation of DNA damage and that rejuvenation is due to the repair of this damage in the micronucleus during meiosis Meiosis appears to be an adaptation for DNA repair and rejuvenation in P tetraurelia 37 In P tetraurelia CtlP protein is a key factor needed for the completion of meiosis during sexual reproduction and recovery of viable sexual progeny 37 The CtlP and Mre11 nuclease complex are essential for accurate processing and repair of double strand breaks during homologous recombination 37 Video gallery Edit source source source source source source source source source source Paramecium bursaria a species with symbiotic algae source source source source source source source source source source Paramecium putrinum source source source source source source source source source source Paramecium binary fission source source source source source source source source Paramecium in conjugation source source source source source source source source source source source source source source Paramecium caudatumList of species EditParamecium aureliaspecies complex Paramecium primaurelia Paramecium biaurelia Paramecium triaurelia Paramecium tetraurelia Paramecium pentaurelia Paramecium sexaurelia Paramecium septaurelia Paramecium octaurelia Paramecium novaurelia Paramecium decaurelia Paramecium undecaurelia Paramecium dodecaurelia Paramecium tredecaurelia Paramecium quadecaurelia Paramecium sonneborniOther species Paramecium buetschlii Paramecium bursaria Paramecium calkinsi Paramecium caudatum Paramecium chlorelligerum Paramecium duboscqui Paramecium grohmannae Paramecium jenningsi Paramecium multimicronucleatum Paramecium nephridiatum Paramecium polycaryum Paramecium putrinum Paramecium schewiakoffi Paramecium woodruffiReferences Edit paramecium Merriam Webster Dictionary a b c Lynn Denis 2008 The Ciliated Protozoa Characterization Classification and Guide to the Literature Springer Science amp Business Media p 30 ISBN 9781402082399 Dobell Clifford 1932 Antony van Leeuwenhoek and his Little Animals 1960 ed New York Dover pp 164 165 ISBN 978 0 486 60594 4 Dolan John R 2019 08 01 Unmasking The Eldest Son of The Father of Protozoology Charles King Protist 170 4 374 384 doi 10 1016 j protis 2019 07 002 ISSN 1434 4610 PMID 31479910 Joblot Louis 1718 Description et usages de Plusieurs Nouveaux Microscopes tant simple que composez in French Vol 2 Paris Jacques Collombat p 79 Hill John 1752 An History of Animals Paris Thomas Osborne p 5 Woodruff Lorande Loss September 1921 The structure life history and intrageneric relationships of Paramecium calkinsi sp nov The Biological Bulletin 41 3 171 180 doi 10 2307 1536748 JSTOR 1536748 Lynn Denis 2008 The Ciliated Protozoa Characterization Classification and Guide to the Literature 3 ed Springer Netherlands ISBN 9781402082382 Wichterman R 2012 12 06 The Biology of Paramecium Springer Science amp Business Media ISBN 9781475703726 a b Curds Colin R Gates Michael Roberts David McL 1983 British and other freshwater ciliated protozoa Vol 2 Cambridge University Press p 126 Esteban Genoveva F Fenchel Tom Finlay Bland J 2010 Mixotrophy in Ciliates Protist 161 5 621 641 doi 10 1016 j protis 2010 08 002 PMID 20970377 Reece Jane B 2011 Campbell Biology San Francisco Pearson Education p 134 ISBN 9780321558237 Blake John R Sleigh Michael A February 1974 Mechanics of ciliary locomotion Biological Reviews 49 1 85 125 doi 10 1111 j 1469 185x 1974 tb01299 x PMID 4206625 S2CID 41907168 Ogura A and K Takahashi Artificial deciliation causes loss of calcium dependent responses in Paramecium 1976 170 172 Katsu Kimura Yumiko et al 2009 Substantial energy expenditure for locomotion in ciliates verified by means of simultaneous measurement of oxygen consumption rate and swimming speed Journal of Experimental Biology 212 12 1819 1824 doi 10 1242 jeb 028894 PMID 19482999 Osterman Natan Vilfan Andrej September 20 2011 Finding the ciliary beating pattern with optimal efficiency PDF Proceedings of the National Academy of Sciences 108 38 15727 15732 arXiv 1107 4273 Bibcode 2011PNAS 10815727O doi 10 1073 pnas 1107889108 PMC 3179098 PMID 21896741 Wichterman R 1986 The Biology of Paramecium Springer US pp 200 1 ISBN 9781475703740 Wichterman Ralph 1985 The Biology of Paramecium New York Plenum Press pp 88 90 ISBN 978 1 4757 0374 0 Reece Jane B et al 2011 Campbell Biology San Francisco Pearson Education p 584 ISBN 9780321558237 Mast S O February 1947 The food vacuole in Paramecium The Biological Bulletin 92 1 31 72 doi 10 2307 1537967 JSTOR 1537967 PMID 20284992 Berger Jacques 1980 Feeding Behaviour of Didinium nasutum on Paramecium bursaria with Normal or Apochlorotic Zoochlorellae Journal of General Microbiology 118 2 397 404 doi 10 1099 00221287 118 2 397 Kreutz Martin Stoeck Thorsten Foissner Wilhelm 2012 Morphological and Molecular Characterization of Paramecium Viridoparamecium nov subgen chlorelligerum Kahl Ciliophora Journal of Eukaryotic Microbiology 59 6 548 563 doi 10 1111 j 1550 7408 2012 00638 x PMC 3866650 PMID 22827482 a b c Preer John R Jr Preer Louise B Jurand Artur June 1974 Kappa and Other Endosymbionts in Paramecium aurelia Bacteriological Reviews 38 2 113 163 doi 10 1128 MMBR 38 2 113 163 1974 PMC 413848 PMID 4599970 Aury Jean Marc Jaillon Oliver Wincker Patrick et al November 2006 Global trends of whole genome duplications revealed by the ciliate Paramecium tetraurelia Nature 444 7116 171 8 Bibcode 2006Natur 444 171A doi 10 1038 nature05230 PMID 17086204 Lekomtsev Sergey Kolosov Petr Bidou Laure Frolova Ludmila Rousset Jean Pierre Kisselev Lev June 26 2007 Different modes of stop codon restriction by the Stylonychia and Paramecium eRF1 translation termination factors Proceedings of the National Academy of Sciences of the United States of America 104 26 10824 9 Bibcode 2007PNAS 10410824L doi 10 1073 pnas 0703887104 PMC 1904165 PMID 17573528 Armus Harvard L Montgomery Amber R Jellison Jenny L Fall 2006 Discrimination Learning in Paramecia P caudatum The Psychological Record 56 4 489 498 doi 10 1007 BF03396029 S2CID 142785414 Ginsburg Simona Jablonka Eva 2009 Epigenetic learning in non neural organisms Journal of Biosciences 34 4 633 646 doi 10 1007 s12038 009 0081 8 PMID 19920348 S2CID 15507569 a b c Prescott D M et al 1971 DNA of ciliated protozoa Chromosoma 34 4 355 366 doi 10 1007 bf00326311 S2CID 5013543 Raikov I B 1972 Nuclear phenomena during conjugation and autogamy in ciliates Research in Protozoology 4 149 Berger James D October 1986 Autogamy inParamecium cell cycle stage specific commitment to meiosis Experimental Cell Research 166 2 475 485 doi 10 1016 0014 4827 86 90492 1 PMID 3743667 Raikov I B 1972 Nuclear phenomena during conjugation and autogamy in ciliates Research in Protozoology 4 151 240 Aufderheide Karl J 1986 Clonal aging in Paramecium tetraurelia II Evidence of functional changes in the macronucleus with age Mechanisms of Ageing and Development 37 3 265 279 doi 10 1016 0047 6374 86 90044 8 PMID 3553762 S2CID 28320562 Smith Sonneborn J 1979 DNA repair and longevity assurance in Paramecium tetraurelia Science 203 4385 1115 1117 Bibcode 1979Sci 203 1115S doi 10 1126 science 424739 PMID 424739 Holmes George E Holmes Norreen R July 1986 Accumulation of DNA damages in aging Paramecium tetraurelia Molecular and General Genetics 204 1 108 114 doi 10 1007 bf00330196 PMID 3091993 S2CID 11992591 Gilley David Blackburn Elizabeth H 1994 Lack of telomere shortening during senescence in Paramecium PDF Proceedings of the National Academy of Sciences of the United States of America 91 5 1955 1958 Bibcode 1994PNAS 91 1955G doi 10 1073 pnas 91 5 1955 PMC 43283 PMID 8127914 Bernstein H Bernstein C 1991 Aging Sex and DNA Repair San Diego Academic Press pp 153 156 ISBN 978 0120928606 a b c Godau Julia Ferretti Lorenza P Trenner Anika Dubois Emeline von Aesch Christine Marmignon Antoine Simon Lauriane Kapusta Aurelie Guerois Raphael Betermier Mireille Sartori Alessandro A 2019 Identification of a miniature Sae2 Ctp1 CtIP ortholog from Paramecium tetraurelia required for sexual reproduction and DNA double strand break repair PDF DNA Repair 77 96 108 doi 10 1016 j dnarep 2019 03 011 PMID 30928893 S2CID 89619084 External links Edit Media related to Paramecium at Wikimedia Commons Data related to Paramecium at Wikispecies Retrieved from https 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