Malus coronaria, also known by the names sweet crabapple or garland crab, is a North American species of Malus (crabapple). It grows primarily in the Great Lakes Region and in the Ohio Valley, with outlying populations as far away as Alabama, eastern Kansas, and Long Island.http://bonap.net/MapGallery/County/Malus%20coronaria.png Malus coronaria often is a bushy shrub with rigid, contorted branches, but frequently becomes a small tree up to 10 meters (33 feet) tall, with a broad open crown. It prefers rich moist soil. Its flowering time is about two weeks later than that of the domestic apple, and its fragrant fruit clings to the branches on clustered stems long after the leaves have fallen.
No narrative description available for this taxon yet.
Compounds documented for Malus coronaria across natural-product and food-composition databases — not just the ~150 nutrients on a classic label ("nutritional dark matter").
🍽 Used in cooking
Compound class profile2 classes
Depsidones1
Depsides1
Documented compounds2 total
Compound
Class
Amount
Source
Atranorin
present
NPASS
Protocetraric acid
present
NPASS
05DNA & barcoding16 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 Malus coronaria has left across the world's sequence archives.
At a glance
DNA specimens16
Marker genes6
eDNA detections15
Countries2
Marker genes sequenced
★ 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★rbcL★rbcLa★ITS★ITS2trnH-psbA
plant barcodefungal barcodemarker
06Genome at a glanceCCDB · GoaT · NCBI
The complete instruction manualMalus coronaria 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 size1 531 059 000 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 Malus coronaria1.53 Gb
HUMAN3.2 Gb
WHEAT17 Gb
FERN Tmesipteris160.45 Gb
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.
Sequencing statusassembly quality — how far to trust these numbers
Assembly level tells you how finished the sequence is — from fragmented contigs, through scaffolds, up to a full chromosome-level assembly. BUSCO % estimates completeness: the share of genes expected to be present that were actually found. These describe the data quality, not the organism.
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 origin5.31 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 type1 416 records
Wild obs. + sensor656
Museum / vouchered632
Cultivated / captive4
Other124
Origin
Native122
Introduced2
Range
Area of Occupancy AOO3 352 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 accuracy75% within 1 km
≤100 m 274≤1 km 40≤10 km 11>10 km 94
419 georeferenced · 237 without coordinates
Open the mapobservation + sensor656
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 accuracy64% within 1 km
≤100 m 62≤1 km 172≤10 km 113>10 km 20
367 georeferenced · 265 without coordinates
Open the institutions mapphysical evidence632
Cultivated / Captivenot free-living
A living individual in a botanical garden, zoo or nursery — cultivated or kept, not free-living.
Coordinate accuracy0% within 1 km
≤10 km 2
2 georeferenced · 2 without coordinates
Open the mapnot free-living4
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 institutions47 of 64 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Bloomington, US
105
Toronto, CA
88
Bronx, US
62
Philadelphia, US
55
Ann Arbor, US
47
Chongqing Museumlocation not on record
43
Saint Louis, US
29
University of Stellenboschlocation not on record
18
Paris, FR
16
Philadelphia, US
16
Royal Botanical Gardenslocation not on record
13
Chapel Hill, US
11
Wuzhou, CN
8
Dekalb, US
7
Chicago, US
6
McWane Science Centerlocation not on record
6
Fort Worth, US
5
Millersville, US
5
Bangkok, TH
5
Auckland, NZ
5
Fairfax, US
3
Tampa, US
3
Museum of the Rockieslocation not on record
3
Richmond, US
3
Royal Ontario Museum, Green Plant Herbarium (TRT)location not on record
3
Dover, US
3
GB
2
Burlington, US
2
Western Carolina Universitylocation not on record
2
Knoxville, US
2
Canadian Department of Agriculturelocation not on record
2
Montréal, CA
2
Williamsburg, US
2
Durham, US
2
University of Southern Mississippilocation not on record
2
Norfolk, US
2
College Park, US
2
Madison, US
2
GAlocation not on record
1
Jackson, US
1
Minia, EG
1
Whitewater, US
1
Little Rock, US
1
Davenport, US
1
DOI/NPS, Greenbelt Parklocation not on record
1
Long Beach, US
1
Cheney, US
1
University of Tennessee at Chattanoogalocation not on record
1
Ypsilanti, US
1
Saint John, CA
1
BClocation not on record
1
China Agricultural Universitylocation not on record
1
Mount Pleasant, US
1
Fredericksburg, US
1
Rotorua, NZ
1
Lord Fairfax Community Collegelocation not on record
1
Columbia, US
1
Jefferson City, US
1
Kirksville, US
1
Chicago, US
1
Institut und Museum fuer Geologie und Palaeontologielocation not on record
1
BAYLUlocation not on record
1
Macomb, US
1
Durham, US
1
64 institutions · 618 of 632 vouchered records shown · 13 without an institution code
Cultivated / Captivenot free-living
A living individual in a botanical garden, zoo or nursery — cultivated or kept, not free-living.
09Environmental DNA15 detections
Where the DNA of Malus coronaria 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 found15
Studies independent surveys1
Countries2
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 15 detections have coordinates
Open the map2 countries0
Dry sandSand and pebbles, dry light brown soil. Prob…
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 median20.5 °C 4.50–22.1
Seasonal swing summer↔winter27.1 °C
Max temp (day)25.1 °C 8.60–25.6
Min temp (night)16.8 °C 0.1–19.5
Precipitation82.9 mm/mo 49.8–86.3
Air humidity59.7 % 59.4–60.2
Moisture balance-57.9 mm/mo -60.5–-24.3
Vapour deficit975 Pa 543–1,080
Wind speed3.20 m/s 2.40–3.40
Cloud cover38.2 % 37.0–52.5
CHELSA 1981–2010, ~9 km grid, at location & month of 4 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.