Myrmecia Printz.
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https://doi.org/10.1080/00318884.2024.2325329 |
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https://doi.org/10.5281/zenodo.15536473 |
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https://treatment.plazi.org/id/5F246365-FFEF-FFFA-7525-F9E44109FDDE |
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Felipe |
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Myrmecia Printz. |
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Myrmecia View in CoL is a coccoid alga with spherical, ovoid, or pear-shaped cells that can form multicellular aggregates. The cell wall may be locally thickened. The chloroplast is parietal, cup-shaped, wavy at the edges, and usually divided into 2–4 lobes ( Fig. 2 View Figs 1–18 ). It reproduces asexually by zoospores, aplanospores or autospores (Ettl & Gärtner 2013). From the nine taxonomically accepted species ( Guiry & Guiry 2022) only two ( M. biatorellae and M. israelensis ) have so far been confirmed as photobionts of Psora View in CoL , Placidium View in CoL and Heteroplacidium View in CoL from the family Verrucariaceae View in CoL ( Thüs et al. 2011; Moya et al. 2018).
Free-living M. biatorellae is often reported from arid regions ( Flechtner et al. 1998; Vinogradova et al. 2004; Flechtner et al. 2008; Venter et al. 2015). However, there are also records from the tundra in north-eastern Russia ( Andreyeva 2005). This species has been reported quite frequently from caves ( Roldán et al. 2004; Vinogradova et al. 2009). For instance, Roldán & Hernández-Mariné (2009) isolated M. biatorellae from a biofilm on the surface of stalactite in Collbató Cave ( Spain). The granite walls of historic buildings in Galicia ( Spain) are also a substrate inhabited by this alga ( Rifón-Lastra & Noguerol-Seoane 2001). In addition to rocks ( Vinogradova et al. 2004), this species often inhabits soil ( Khaybullina et al. 2010; Bakieva et al. 2012), tree bark ( Khaybullina et al. 2010), sand ( Schulz et al. 2016) and survives on serpentinite soils ( Venter et al. 2015).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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