Gonium

Gonium
Gonium pectorale Mueller
Scientific classification
Domain: Eukaryota
Kingdom: Plantae
Division: Chlorophyta
Class: Chlorophyceae
Order: Volvocales
Family: Goniaceae
Genus: Gonium
O. F. Muller, 1773
Species
  • Gonium maiaprilis
  • Gonium multicoccum
  • Gonium octonarium
  • Gonium pectorale
  • Gonium quadratum
  • Gonium sacculiferum
  • Gonium sociale
  • Gonium viridistellatum
Gonium colony of 16 cells at nominal magnification of 450x.

Gonium is a genus of colonial algae, a member of the order Volvocales. Typical colonies have 4 to 16 cells, all the same size, arranged in a flat plate, with no anterior-posterior differentiation. In a colony of 16 cells, four are in the center, and the other 12 are on the four sides, three each.[1] A description by G.M. Smith (1920, p. 94):[2]

Gonium Mueller 1773: Colonies of 4-8-16 cells arranged in a flat quadrangular plate and embedded in a common gelatinous matrix or connected by broad gelatinous strands. Cells ovoid to pyriform, with a single cup-shaped chloroplast containing one pyrenoid. Each cell with two cilia of equal length, contractile vacuoles at the base of the cilia, and an eyespot. Four- and eight-celled colonies with the cilia on the same side ; sixteencelled colonies with the four central cells having their cilia on the same side and the twelve marginal cells with radially arranged cilia.

Asexual reproduction by simultaneous division of all cells in the colony to form autocolonies, or by a formation of 2-4 zoospores in each cell.

Sexual reproduction isogamous, by a fusion of biciliate zoogametes.

Evolution

The genus Gonium represents species closely related to single celled Chlamydomonas and multicellular differentiated Volvox. The order Volvocales has long been a well recognized model system for the study of multicellular evolution. Gonium and the genus Tetrabaenecae contain species representative of colony formation among unicells. Gonium's morphology of colonies of alike cells suggest it is more genetically similar to Chlamydomonas than Volvox, a fact confirmed by phylogenetic analysis.[3]

The Volvocales have been hypothesized to have evolved in twelve discrete steps.[4] Gonium represents the first six evolutionary steps of multicellularity;[3] (1) incomplete cytokinesis, (2) partial inversion, (3) rotation of the basal bodies, (4) organismal polarity, (5) transformation of the cell wall into extra-cellular matrix (ECM), (6) genetic control of cell number. Although the exact order and progression through David Kirk's twelve steps of multicellular evolution [4] are probably not necessarily linear and each occurs more dynamically than originally thought.[3]

Life cycle

Gonium being evolutionarily related to Chlamydomonas has a life cycle that is derivative of that of Chlamydomonas. Gonium cells grow asexually as colonies of either 4, 8 or 16 colonial cells. Cell and colony growth of Gonium is uncoupled from cell division just like Chlamydomonas and each cell within the colony divides by multiple-fission. Thus, each cell within the colony will divide 2, 3 or 4 times, thus producing 2"n" daughter cells, or 4, 8 or 16 cells within the colony. Unlike Chlamydomonas where each of the daughter cells separate from each other, Gonium daughter cells remain attached to each other in their ECM.

The sexual cycle of Gonium is also very similar to that of Chlamydomonas. The sexual program of Gonium is induced by nitrogen deprivation where each vegetative cell within the colony differentiates in gametes. Gonium gametes are isogomous, or equal-sized, and unicellular. Thus unicellular Gonium gametes break apart from the multicellular colonies when the sexual program is initiated. Also like Chlamydomonas, there are two "sexes", plus or minus controlled by a genes homologous [5] to those found in Chlamydomonas and Volvox.[6]

References

  1. Pennak, Robert W (1978). Fresh-Water Invertebrates of the United States (Second ed.). John Wiley & Sons. p. 43. ISBN 0-471-04249-8.
  2. Smith, GM. Phytoplankton of Inland Lakes of Wisconsin, Part I, Wisconsin Geological and Natural History Survey, Madison, WI. (1920).
  3. 1 2 3 Herron MD, Hackett JD, Aylward FO, Michod RE (2009). "Triassic origin and early radiation of multicellular volvocine algae". Proceedings of the National Academy of Sciences, USA. 106: 3254–3258. doi:10.1073/pnas.0811205106.
  4. 1 2 Kirk, DL (2005). "A twelve-step program for evolving multicellularity and a division of labor". BioEssays. 27 (3): 299–310. doi:10.1002/bies.20197. PMID 15714559.
  5. Hamaji, T., Ferris, P. J., Coleman, A. W., Waffenschmidt, S., Takahashi, F., Nishii, I., & Nozaki, H. (2008). "Identification of the minus-dominance gene ortholog in the mating-type locus of Gonium pectoral". Genetics. 178 (1): 283–294. doi:10.1534/genetics.107.078618.
  6. Ferris, P. J., Olson, B., de Hoff, P. L., Douglass, S., Casero, D., Prochnik, S. E., Geng, S.; et al. (2010). "Evolution of an expanded sex-determining locus in Volvox". Science. 328 (5976): 351–354. doi:10.1126/science.1186222. PMC 2880461Freely accessible. PMID 20395508.
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