Dalea mollissima is a desert wildflower plant in the legume family (Fabaceae), with the common names soft prairie clover, downy dalea, and silk dalea.Mojave Desert Wildflowers, Pam MacKay, 2nd ed., 2013, DesertUSA: Silky Dalea, soft prairie clover, downy dalea
No narrative description available for this taxon yet.
A DNA barcode is a short, standardised stretch of genes that works like a fingerprint — enough to tell one species from another. Below is the molecular trace Dalea mollissima has left across the world's sequence archives.
At a glance
DNA specimens4
Marker genes4
GenBank sequences2
eDNA detections3
Countries1
The DNA barcodea real sequence read deposited for this species
★ the standard DNA barcode for this group — the short region actually read to tell this species apart. The rest are extra genes sequenced along the way.
★matK1★rbcLa★ITS1★ITS2
plant barcodefungal barcode
06Genome at a glanceCCDB
The complete instruction manualDalea mollissima carries — its genome. We read it from three angles — how big it is, how the DNA is packed into chromosomes, and how completely it has been sequenced — and explain how to read each value as you go.
Chromosomes & ploidyhow the DNA is packaged
2n is the full chromosome count in a normal body cell; n is a gamete (egg or sperm), which carries half. Ploidy is how many complete chromosome sets each cell holds — 2× (diploid) is typical for animals, while higher levels (polyploidy) are common in plants. Click any value below to see the underlying records and sources.
How far back this lineage goes — and how we know. Everything here is measured in Ma, short for “mega-annum”: millions of years ago. The chart reads left to right like a calendar of the Earth, from the deep past on the left to today at the right edgetop to bottom like a core drilled through the Earth, from the deep past at the top down to today at the bottom.
At a glance
DNA clock origin13.6 Ma TimeTree
When this lineage existed
How to read this: the coloured strip along the bottomdown the left is the geological calendar — the standard epochs (Pliocene, Pleistocene…) every museum uses, shown so you can see which chapter of Earth's history this lineage lived in. This lineage is a young one, so the strip is zoomed in to epochs — the finer subdivisions inside a period. The orange marker is the DNA clock: DNA accumulates mutations at a roughly steady rate, so comparing this species' DNA with its relatives estimates when the lineage split off — independently of any fossil.
DNA clock origin
08Occurrence & distribution
Record type2 327 records
Wild obs. + sensor1 733
Museum / vouchered594
Origin
Native131
Range
Area of Occupancy AOO5 004 km²
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Coordinate accuracy90% within 1 km
≤100 m 937≤1 km 101≤10 km 57>10 km 59
1 154 georeferenced · 579 without coordinates
Open the mapobservation + sensor1 733
Museum / Voucheredphysical evidence
Backed by a physical specimen — a herbarium sheet, sample or voucher held in a collection. “Vouchered” means supported by material evidence, not just an observation.
Coordinate accuracy46% within 1 km
≤100 m 29≤1 km 64≤10 km 107>10 km 4
204 georeferenced · 390 without coordinates
Open the institutions mapphysical evidence594
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
10Collections & institutions
Holding institutions35 of 47 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Claremont, US
147
Riverside, US
123
San Diego, US
81
ASUlocation not on record
41
Bronx, US
28
Flagstaff, US
17
Phoenix, US
14
Davis, US
12
Provo, US
9
Henderson, US
8
Irvine, US
7
Arcata, US
6
Severin-McDaniel Insect Collectionlocation not on record
4
DOI/NPS, Little Rock Central High School National Historic Sitelocation not on record
4
Canadian Department of Agriculturelocation not on record
4
Santa Barbara, US
4
Los Angeles, US
3
Angwin, US
3
US
3
Ensenada, MX
3
CASlocation not on record
3
Wuzhou, CN
2
La Paz, MX
2
Fullerton, US
2
San Luis Obispo, US
2
Long Beach, US
2
Austin, US
2
Arizona Western Collegelocation not on record
2
Orem, US
2
EL PASO, US
2
Northridge, US
2
LDlocation not on record
2
Fredericton Stock Culture Collectionlocation not on record
1
Moscow, US
1
Boise, US
1
Facultad de Zootecnia y Ecología, Universidad Autónoma de Chihuahualocation not on record
1
Logan, US
1
Frankfurt am Main
1
Mexico City, MX
1
DOI/NPS, Colonial National Historical Parklocation not on record
1
Chadron, US
1
San Francisco, US
1
Saint Louis, US
1
The University of Arizonalocation not on record
1
Calabar, NG
1
San Diego Natural History Museum, Herbariumlocation not on record
1
Hermosillo, MX
1
47 institutions · 561 of 594 vouchered records shown · 33 without an institution code
09Environmental DNA3 detections
Where the DNA of Dalea mollissima was picked up in samples of water, soil or air — nobody saw the organism, only its DNA left behind. A trace is a clue that the species was near, not a confirmed sighting.
Signal
Detections DNA found3
Studies independent surveys1
Countries1
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 3 detections have coordinates
Open the map1 country0
How strong is each trace?
DNA read depthRead counts were not reported for this species — the map shows presence only, not how strong each trace was.
Modelled climatemodelled
−15°Ctemperature across detection sites+40°C
Temperature median22.6 °C 22.6–22.6
Seasonal swing summer↔winter20.0 °C
Max temp (day)29.7 °C
Min temp (night)15.5 °C
Precipitation5.00 mm/mo
Air humidity43.1 %
Moisture balance-186 mm/mo
Vapour deficit1,560 Pa
Wind speed4.80 m/s
Cloud cover28.6 %
CHELSA 1981–2010, ~9 km grid, at location & month of 1 detection point · median with p10–p90 · reflects where sampling happened, not only the true niche
How to read this: each dot is one detection of this species' DNA in an environmental sample. The confidence meter weighs how many independent studies and places back up the signal — one detection in one study is a hint; many across several studies is solid. Records dated before 2008 (when eDNA methods began) are treated as likely mislabeled and left off the map.