Minorisa
| Minorisa | |
|---|---|
Scientific classification 
| |
| Domain: | Eukaryota |
| Clade: | Diaphoretickes |
| Clade: | SAR |
| Phylum: | Cercozoa |
| Class: | Chlorarachniophyceae |
| Order: | Minorisida |
| Family: | Minorisidae |
| Genus: | Minorisa del Campo, 2013 [1] |
| Species: | M. minuta
|
| Binomial name | |
| Minorisa minuta del Campo [1]
| |
Minorisa is a monotypic genus of marine heterotrophic flagellates that is heavily featured in the eukaryotic picoplankton of coastal ecosystems.[1] It is part of the supergroup Rhizaria, at the base of the class Chlorarachniophyceae.[1]
Etymology[edit]
The name Minorisa comes from the town Manresa, the birthplace of Javier del Campo, who first described the genus in 2013.[1] Minuta, latin for tiny, refers to the small size of the organism.[1]
History of knowledge[edit]
Culturing bias is the tendency to study organisms that are easily cultured and this bias was rampant in the past study of protist phylogeny, ecology, and evolution.[2] There are a myriad of reasons why organisms may be reluctant to culturing. Heterotrophic protists are particularly difficult to culture because culturing a heterotroph necessitates knowing its prey and culturing it consecutively. Another reason why organisms may be reluctant to culturing is due to size. Organisms that are only micrometers long tend to pass through the plankton nets that are typically used by oceanographers to survey they microscopic organisms living in bodies of water.
One way that scientists attempt to overcome culturing bias is by using environmental sequencing, a method that determines the genetic sequence everything found in a sample of water, rather than only the cells scooped up by a plankton net.[3] Environmental sequencing aims to isolate organisms that are reluctant to being cultured but are abundant in the environment.[1] One such environmental sequencing study captured an unknown rhizarian when attempting to culture ecologically relevant heterotrophic flagellates off the coast of Spain.[1] The rhizarian isolate was genetically distant from any described species, but it matched environmental sequences from the Mediterranean Sea, the Sargasso Sea, and the English Channel.[1] This rhizarian was named Minorisa minuta and thus the genus Minorisa was born.[1]
Habitat and ecology[edit]
Minorisa minuta are marine heterotrophic flagellates that swim and are active bacterial grazers.[1] They are well adapted to low prey abundances and very efficient at ingesting bacteria.[4] They are widely distributed and abundant in oceans worldwide, accounting for up to 5% of all heterotrophic flagellates in the world.[1] [5] Minorisa are present in ocean all year long particularly near coastal areas,[1] though abundances vary depending on site, suggesting pockets of population density.[6]
Description of organism[edit]
Morphology and anatomy[edit]
Minorisa minuta is a unicellular organism with naked and spherical ovoid cells.[1] They are minuscule, only ~1.3 micrometers wide and ~1.5 micrometers long.[1] This explains why Minorisa had not been picked up by other survey methods, since most nets used to capture protists are not fine enough to trap such a tiny organism. Minorisa possesses a single flagellum that could be up to four times its length.[1]
Life cycle[edit]
The life cycle of Minorisa minuta is unknown.
Genetics and phylogeny[edit]
Molecular phylogenetics places Minorisa minuta at the base of the Chlorarachniophytes.[1] Minorisa is the only heterotrophic representative within the Chlorarachniophytes, which is the only photosynthetic group within the supergroup Rhizaria.[1] It is unknown whether Minorisa posteriorly lost the plastid or whether the lack of a plastid in Minorisa indicates a second instance of acquisition of a green plastid independently in Chlorarachniophytes.[1]
Practical importance[edit]
Minorisa represents one of the main players in the eukaryotic picoplankton of coastal ecosystems, possibly having a relevant role in carbon fluxes and controlling bacterial populations.[1] Minorisa in coastal waters could be as important as MAST (marine stramenopiles) in open ocean, considered abundant bacterivores.[1]
References[edit]
- ^ a b c d e f g h i j k l m n o p q r s t u del Campo, Javier; Not, Fabrice; Forn, Irene; Sieracki, Michael E.; Massana, Ramon (2013). "Taming the smallest predators of the oceans". The ISME Journal. 7 (2): 351–358. doi:10.1038/ismej.2012.85. ISSN 1751-7370. PMC 3554395. PMID 22810060.
- ^ del Campo, Javier; Balagué, Vanessa; Forn, Irene; Lekunberri, Itziar; Massana, Ramon (2013-10-01). "Culturing Bias in Marine Heterotrophic Flagellates Analyzed Through Seawater Enrichment Incubations". Microbial Ecology. 66 (3): 489–499. doi:10.1007/s00248-013-0251-y. ISSN 1432-184X. PMID 23749062. S2CID 253778653.
- ^ del Campo, Javier; Guillou, Laure; Hehenberger, Elisabeth; Logares, Ramiro; López-García, Purificación; Massana, Ramon (2016-08-01). "Ecological and evolutionary significance of novel protist lineages". European Journal of Protistology. Current trends in protistology – results from the VII ECOP - ISOP Joint Meeting 2015. 55 (Pt A): 4–11. doi:10.1016/j.ejop.2016.02.002. ISSN 0932-4739. PMC 5242370. PMID 26996654.
- ^ Rodríguez‐Martínez, Raquel; Vaqué, Dolors; Forn, Irene; Massana, Ramon (2022). "Dominant marine heterotrophic flagellates are adapted to natural planktonic bacterial abundances". Environmental Microbiology. 24 (5): 2421–2434. doi:10.1111/1462-2920.15911. ISSN 1462-2912. PMC 9303649. PMID 35080092.
- ^ Burki, Fabien; Keeling, Patrick J. (2014). "Rhizaria". Current Biology. 24 (3): R103–R107. doi:10.1016/j.cub.2013.12.025. ISSN 0960-9822. PMID 24502779. S2CID 235312055.
- ^ Giner, Caterina R.; Forn, Irene; Romac, Sarah; Logares, Ramiro; de Vargas, Colomban; Massana, Ramon (2016). "Environmental Sequencing Provides Reasonable Estimates of the Relative Abundance of Specific Picoeukaryotes". Applied and Environmental Microbiology. 82 (15): 4757–4766. Bibcode:2016ApEnM..82.4757G. doi:10.1128/AEM.00560-16. ISSN 0099-2240. PMC 4984273. PMID 27235440.