Corpus ID: 164208605

Nomenclatural changes in Chenopodium ( incl . Rhagodia ) ( Chenopodiaceae ) , with considerations on relationships of some Australian taxa and their possible Eurasian relatives

@inproceedings{Mosyakin2017NomenclaturalCI,
  title={Nomenclatural changes in Chenopodium ( incl . Rhagodia ) ( Chenopodiaceae ) , with considerations on relationships of some Australian taxa and their possible Eurasian relatives},
  author={Sergei L. Mosyakin and Duilio Iamonico},
  year={2017}
}
Mosyakin, S.L. & Iamonico, D. Nomenclatural changes in Chenopodium (incl. Rhagodia) (Chenopodiaceae), with considerations on relationships of some Australian taxa and their possible Eurasian relatives. Nuytsia 28: 255–271 (2017). Following recent molecular phylogenetic results, species earlier placed in Rhagodia R.Br. were transferred to Chenopodium L. (Chenopodiaceae). However, three new species-level combinations proposed were later homonyms and thus illegitimate under ICN Art. 53.1. The new… Expand
Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments
TLDR
The phylogenetic results, as well as presence of the stalactites in the outer cell walls of the testa and lack of the rosulate leaves, confirm the distinctive nature of Monolepisspathulata from all Blitum and, therefore, the recent combination Blitumaspathulatum cannot be accepted. Expand
A Chromosome-Scale Assembly of the Garden Orach (Atriplex hortensis L.) Genome Using Oxford Nanopore Sequencing
TLDR
The assembly of the first high-quality, chromosome-scale reference genome for A. hortensis is reported, which identifies three distinct populations with little variation within subpopulations. Expand
Inventory of orchids in Polewali Mandar , West Sulawesi , Indonesia DWI MURTI
Puspitaningtyas DM. 2019. Inventory of orchids in Polewali Mandar, West Sulawesi, Indonesia. Biodiversitas 20: 1887-1896. Sulawesi is the fourth largest island in Indonesia. It is also a uniqueExpand

References

SHOWING 1-10 OF 59 REFERENCES
A novel phylogeny-based generic classification for Chenopodium sensu lato, and a tribal rearrangement of Chenopodioideae (Chenopodiaceae)
TLDR
The present study provides a modern classification for a globally distributed group of plants that had suffered a complex taxonomic history due to divergent interpretation of single morphological characters for more than two hundred years. Expand
NEW NOMENCLATURAL COMBINATIONS IN BLITUM , OXYBASIS, CHENOPODIASTRUM , AND LIPANDRA (CHENOPODIACEAE)
TLDR
Following the recent recognition of several genera segregated from Chenopodium sensu lato (Chenopodiaceae), new nomenclatural combinations are proposed in the genera Blitum L. nov., Chenopodiastrum fasciculosum (Aellen), and Lipandra. Expand
Taxonomic revision of Chenopodiaceae in Nepal
A taxonomic revision of the family Chenopodiaceae in Nepal with new diagnostic keys, descriptions and detailed distribution patterns is here presented for the first time. 24 species from 13 generaExpand
Molecular phylogeny of Atripliceae (Chenopodioideae, Chenopodiaceae): Implications for systematics, biogeography, flower and fruit evolution, and the origin of C4 photosynthesis.
UNLABELLED PREMISE OF THE STUDY Atripliceae (Chenopodiaceae), including Atriplex (300 spp.) as the largest genus of the family, are an ecologically important group of steppes and semidesertsExpand
Phylogenetic analysis of the Australian Salicornioideae (Chenopodiaceae) based on morphology and nuclear DNA
TLDR
The current tribal classification of the Salicornioideae was not supported in the molecular analysis and three major clades received strong bootstrap support: Microcnemum+Arthrocnemum, Sarcocornia+Salicornia, and the endemic Australian genera. Expand
Towards a species level tree of the globally diverse genus Chenopodium (Chenopodiaceae).
TLDR
The tribe Dysphanieae with three genera Dysphania, Teloxys and Suckleya is now shown to form one of the early branches in the tree of Chenopodioideae, and the tribe Spinacieae is recognized to include Spinacia, several species of Chenipodium, andthe genera Monolepis and Scleroblitum. Expand
New combinations in Asiatic Oxybasis (Amaranthaceae s.l.): evidence from morphological, carpological and molecular data
TLDR
Molecular phylogenetic analysis using maximum likelihood (ML) and maximum parsimony (MP) methods confirmed the placement of C. micranthum and C. gubanovii in the genus Oxybasis. Expand
Fruit and Seed Anatomy of Chenopodium and Related Genera (Chenopodioideae, Chenopodiaceae/Amaranthaceae): Implications for Evolution and Taxonomy
A comparative carpological study of 96 species of all clades formerly considered as the tribe Chenopodieae has been conducted for the first time. The results show important differences in theExpand
Phylogeny of the Australian Camphorosmeae (Chenopodiaceae) and the Taxonomic Significance of the Fruiting Perianth
TLDR
Phylogenetic hypotheses inferred from molecular data do not support the current taxonomy of Camphorosmeae in Australia, and Neobassia, Threlkeldia, Osteocarpum, and Enchylaena should be subsumed into the species‐rich genera Sclerolaena and Maireana. Expand
Origin and age of Australian Chenopodiaceae.
TLDR
It is concluded that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae and Salsoleae. Expand
...
1
2
3
4
5
...