Compounds documented for Aechmea bracteata across natural-product and food-composition databases — not just the ~150 nutrients on a classic label ("nutritional dark matter").
Compound class profile1 class
Anthocyanidins2
Documented compounds2 total
Compound
Class
Amount
Source
cyanidin-3,5-diglucoside
present
LOTUS
05DNA & barcoding4 specimens
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 Aechmea bracteata has left across the world's sequence archives.
At a glance
DNA specimens4
Marker genes3
GenBank sequences3
eDNA detections2
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.
★matK2★rbcL1★rbcLa
plant barcode
06Genome at a glanceGoaT
The complete instruction manualAechmea bracteata 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.
Genome sizehow big the whole instruction manual is
Genome size396 090 000 bp
Measured in base pairs (bp) — the individual letters of DNA (human ≈ 3.2 Gb, a bacterium a few million). The chart places this genome on a logarithmic scale — each step to the right is ten times bigger — among reference organisms. Across species a bigger genome loosely tracks with larger cells, slower growth and lower-energy lifestyles (powered flight favours small genomes) — yet it does not imply more genes or a more advanced organism (the long-standing C-value paradox).
BACTERIUM Carsonella ruddii0.00016 Gb
FUNGUS0.04 Gb
INSECT0.25 Gb
THIS GENOME Aechmea bracteata0.40 Gb
HUMAN3.2 Gb
WHEAT17 Gb
FERN Tmesipteris160.45 Gb
08Occurrence & distribution
Record type2 212 records
Wild obs. + sensor1 405
Museum / vouchered799
Other8
Range
Area of Occupancy AOO4 412 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 accuracy85% within 1 km
≤100 m 599≤1 km 274≤10 km 105>10 km 54
1 032 georeferenced · 373 without coordinates
Open the mapobservation + sensor1 405
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 accuracy94% within 1 km
≤100 m 347≤1 km 22≤10 km 24>10 km 1
394 georeferenced · 405 without coordinates
Open the institutions mapphysical evidence799
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 institutions38 of 57 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Durango, MX
223
Mexico City, MX
109
Saint Louis, US
96
Chicago, US
71
Mérida, MX
25
Universidad Juárez Autónoma de Tabascolocation not on record
21
Tampa, US
20
Austin, US
19
Provincia di Livornolocation not on record
18
National Biodiversity Institute, Costa Ricalocation not on record
17
San Francisco de Campeche, MX
14
Ciudad de México, MX
11
Ann Arbor, US
11
Mérida, MX
11
Bronx, US
10
León, NI
9
Madison, US
9
Tuxtla Gutiérrez, MX
8
San José, CR
7
Tapachula, MX
7
Mexico City, MX
6
Riverside, US
6
Juriquilla, MX
4
Mexico City, MX
3
NO DISPONIBLElocation not on record
3
University of Stellenboschlocation not on record
3
Austin, US
3
San Jose State University, Museum of Birds and Mammalslocation not on record
3
Kew, GB
2
MAlocation not on record
2
GB
2
San Francisco, US
2
Tuxtla Gutiérrez, MX
2
Universidad Nacional Autonoma de Mexico, Instituto de Biologialocation not on record
2
Instituto de Investigaciones Biológicas, Universidad Veracruzana, Región Xalapalocation not on record
2
JBRJlocation not on record
2
LDlocation not on record
2
South Kensington, GB
2
Puebla, MX
2
Chapingo, MX
2
San Luis Potosí, MX
2
Zapopan, MX
1
Universidad Autónoma de Nayaritlocation not on record
1
University of California at Berkeleylocation not on record
1
Autlán de Navarro, MX
1
Centro de Investigaciones Biológicas, Universidad Autónoma del Estado de Hidalgolocation not on record
1
Cambridge, US
1
Calabar, NG
1
College Park, US
1
Guasave, MX
1
Pomona Collegelocation not on record
1
MEXUlocation not on record
1
Giardini Botanici Hanburylocation not on record
1
Paris, FR
1
Station d'Ecologie de Lamtolocation not on record
1
College of the Atlantic, Museumlocation not on record
1
Claremont, US
1
57 institutions · 789 of 799 vouchered records shown · 10 without an institution code
09Environmental DNA2 detections
Where the DNA of Aechmea bracteata 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 found2
Studies independent surveys1
Countries1
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 2 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 median27.3 °C 26.9–27.6
Seasonal swing summer↔winter5.50 °C
Max temp (day)31.9 °C 31.3–32.4
Min temp (night)23.4 °C 23.1–23.7
Precipitation152 mm/mo 152–152
Air humidity64.5 % 63.6–65.4
Moisture balance-1.90 mm/mo -4.30–0.5
Vapour deficit1,288 Pa 1,228–1,347
Wind speed1.80 m/s 1.80–1.90
Cloud cover27.3 % 27.2–27.5
CHELSA 1981–2010, ~9 km grid, at location & month of 2 detection points · 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.