Triteleia grandiflora is a species of flowering plant known by the common names largeflower triteleia, largeflower tripletlily, and wild hyacinth. It is native to western North America from British Columbia to extreme northern California, eastward into Idaho, Montana and northern Utah, with disjunct populations occurring in Wyoming and Colorado.Ladyman, J. (2007). Triteleia grandiflora: A technical conservation assessment. US Forest Service.Biota of North America Program, 2013 county distribution map Its habitat includes grassland, sagebrush, woodlands, and forests. It is a perennial herb growing from a corm. It produces two or three basal leaves up to 70 cm long by 1 cm wide. The inflorescence arises on a smooth, erect stem up to tall and bears an umbel-like cluster of many flowers. Each flower is a funnel-shaped bloom borne on a pedicel up to 4 or 5 cm long. The flower may be up to 3.5 cm long including the tubular throat and six tepals each just over 1 cm long. The inner set of three tepals are somewhat ruffled and broader than the outer tepals. The flower corolla may be deep blue to almost white with a darker blue mid-vein. There are six stamens with purple or yellow anthers. With tubular throat and six tepals, the flower contains six stamens with purple or yellow anthers. The corm provides food for various wild rodents and livestock, and Native Americans and settlers found them edible as well.
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 Triteleia grandiflora has left across the world's sequence archives.
At a glance
DNA specimens2
Marker genes3
GenBank sequences1
eDNA detections1
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.
★matK★rbcL1★rbcLa
plant barcode
06Genome at a glanceGoaT
The complete instruction manualTriteleia grandiflora 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.
Ploidypolyploid inferred
Ploidy records — measured levels and diploid/polyploid inferences · click for sources
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Coordinate accuracy87% within 1 km
≤100 m 1 988≤1 km 311≤10 km 171>10 km 163
2 633 georeferenced · 671 without coordinates
Open the mapobservation + sensor3 304
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 accuracy48% within 1 km
≤100 m 44≤1 km 189≤10 km 227>10 km 28
488 georeferenced · 579 without coordinates
Open the institutions mapphysical evidence1 067
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 institutions37 of 51 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Pullman, US
287
WTUlocation not on record
164
Corvallis, US
143
Moscow, US
66
Missoula, US
47
Victoria, CA
45
Bronx, US
42
Logan, US
36
Boise, US
36
Bozeman, US
23
Vancouver, CA
22
Tacoma, US
19
Caldwell, US
12
US
12
Cheney, US
11
Provo, US
10
Pocatello, US
9
Chongqing Museumlocation not on record
9
Wuzhou, CN
8
Portland, US
7
ASUlocation not on record
6
Claremont, US
6
Riverside, US
5
DOI/NPS, Little Rock Central High School National Historic Sitelocation not on record
4
Bloomington, US
4
Pittsburg, US
3
Phoenix, US
3
Weber State Universitylocation not on record
2
Auckland, NZ
2
Orem, US
2
CASlocation not on record
1
China Agricultural Universitylocation not on record
1
Saint Louis, US
1
Durham, US
1
Université Lavallocation not on record
1
Flagstaff, US
1
Moscow State Universitylocation not on record
1
Kew, GB
1
Bureau of Land Management, Medford District Officelocation not on record
1
GB
1
University of British Columbia, Herbariumlocation not on record
1
Philadelphia, US
1
Mexico City, MX
1
Henderson, US
1
University of Stellenboschlocation not on record
1
Museo civico La Terra e l'Uomo di Crocetta del Montellolocation not on record
1
University of Alberta Museumslocation not on record
1
Albuquerque, US
1
Austin, US
1
Northridge, US
1
Santa Barbara, US
1
51 institutions · 1 066 of 1 067 vouchered records shown · 1 without an institution code
09Environmental DNA1 detections
Where the DNA of Triteleia grandiflora 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 found1
Studies independent surveys1
Countries1
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 1 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 median7.50 °C 7.50–7.50
Seasonal swing summer↔winter21.3 °C
Max temp (day)13.2 °C
Min temp (night)1.00 °C
Precipitation68.4 mm/mo
Air humidity51.9 %
Moisture balance-36.3 mm/mo
Vapour deficit499 Pa
Wind speed2.10 m/s
Cloud cover41.6 %
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.