Arachis glabrata
TaxID: 212810
Basic Information
Arachis glabrata
Perennial Peanut, Rhizoma peanut, perennial peanut
Arachis glabrata (creeping forage peanut, rhizoma peanut, rhizoma perennial peanut, perennial forage peanut, golden glory, ornamental peanut grass) is a high-quality forage plant native to Argentina, Brazil, and Paraguay vegetation. This plant is also used for soil conservation and as an ornamental plant. It is adapted to sandy soils in the Gulf Coast region of the United States. It is often cultivated together as a following grass species: Axonopus affinis, Axonopus fissifolius, Brachiaria decumbens, Cynodon dactylon, Digitaria eriantha, Paspalum nicorae, and Paspalum notatum. These legume species are also cited as a companion species: Aeschynomene villosa, Medicago sativa, and Trifolium repens. It is a warm-season, perennial legume.
from Wikipedia
Taxonomic Information
Eukaryota
Streptophyta
Magnoliopsida
Fabales
Fabaceae
Arachis
glabrata
Unclassified
Species
nan
d__Eukaryota;p__Streptophyta;c__Magnoliopsida;o__Fabales;f__Fabaceae;g__Arachis;s__Arachis glabrata
nan
Weeds
Photos (0 photos)
No photos available.
Morphological Features
No morphological description available.
Host Plants (0 host plants)
Data sources: EPPO Global Database and relevant literature.
No host plants available.
Quarantine Status (2 records)
Data sources: IPPC website and national quarantine websites; verified by human review.
| Country | Status | Year Added |
|---|---|---|
| Nicaragua | Absent | — |
| United States of America | Quarantine pests | — |
Distribution (10 countries)
Data Sources: EPPO Global Database and GBIF.
| Country | Status | State |
|---|---|---|
| Argentina | Present | — |
| Bolivia (Plurinational State of) | Present | — |
| Brazil | Present | — |
| Democratic Republic of the Congo | Present | — |
| Costa Rica | Present | — |
| Dominican Republic | Present | — |
| Malaysia | Present | — |
| Paraguay | Present | — |
| Uruguay | Present | — |
| United States of America | Present | — |
Distribution Map (Latitude and longitude coordinates sourced from GBIF.)
Download CSVGenomes (0 records)
Data source: NCBI.
No genome records available.
Transcriptomes (3 records)
Data source: NCBI.
| Run ID | Tissue | Developmental Stage | Sex | Read Count | Location | Actions |
|---|---|---|---|---|---|---|
| SRR12976768 | seedings | - | - | 23024714 | China: Nanning, Guangxi Province | |
|
PRJNA674465 SRX9428926 SRP291062 weed RNA-seq of Arachis glabrata The PacBio SMRT sequencing library was constructed using equally mixed RNAs from different tissues. First-strand cDNA was synthesized using UMI base PCR cDNA Synthesis Kit (BGI). After synthesis of first strand, PCR amplification was performed to generate double-strand cDNA. Then, the cDNA was used for optional size selection for constructing a combined SMRTbell library. The library was subsequently sequenced using a PacBio sequel system. {'tissue': 'seedings', 'replicate': 'biological replicate 1', 'treatment': 'The seedings were grown at 28℃.', 'geo_loc_name': 'China: Nanning, Guangxi Province', 'biosamplemodel': 'Plant'} |
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| SRR12976767 | seedings | - | - | 22942210 | China: Nanning, Guangxi Province | |
|
PRJNA674465 SRX9428927 SRP291062 weed RNA-seq of Arachis glabrata The PacBio SMRT sequencing library was constructed using equally mixed RNAs from different tissues. First-strand cDNA was synthesized using UMI base PCR cDNA Synthesis Kit (BGI). After synthesis of first strand, PCR amplification was performed to generate double-strand cDNA. Then, the cDNA was used for optional size selection for constructing a combined SMRTbell library. The library was subsequently sequenced using a PacBio sequel system. {'tissue': 'seedings', 'replicate': 'biological replicate 2', 'treatment': 'The seedings were grown at 28℃.', 'geo_loc_name': 'China: Nanning, Guangxi Province', 'biosamplemodel': 'Plant'} |
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| SRR12976756 | seedings | - | - | 21237663 | China: Nanning, Guangxi Province | |
|
PRJNA674465 SRX9428938 SRP291062 weed RNA-seq of Arachis glabrata The PacBio SMRT sequencing library was constructed using equally mixed RNAs from different tissues. First-strand cDNA was synthesized using UMI base PCR cDNA Synthesis Kit (BGI). After synthesis of first strand, PCR amplification was performed to generate double-strand cDNA. Then, the cDNA was used for optional size selection for constructing a combined SMRTbell library. The library was subsequently sequenced using a PacBio sequel system. {'tissue': 'seedings', 'replicate': 'biological replicate 3', 'treatment': 'The seedings were grown at 28℃.', 'geo_loc_name': 'China: Nanning, Guangxi Province', 'biosamplemodel': 'Plant'} |
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DNA Barcodes (1 records)
View allData source: BOLD.
| Process ID | BIN | Marker | Length | Country | Date | Lat/Lon | Sequence |
|---|---|---|---|---|---|---|---|
| GBITS57390-21 | - | ITS | 582 | - | - | - |
Literature
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