Dipodomys merriami
Mearns, 1890 · speciesAt a glance
Sources12 archives
Databases and archives Dipodomys merriami's data was compiled from.
WikipediaWikimedia Foundation11 languages↗
Animal Diversity WebUniv. of Michigan MZspecies account↗
BioWikiNetmultilingual Wikipediamultilingual↗
GBIFGlobal Biodiversity Information Facility13 727 records↗
ENAEuropean Nucleotide Archive · EMBL-EBI220 eDNA detections↗
BOLD SystemsCentre for Biodiversity Genomics161 specimens↗
Open Tree of LifeOpenTreephylogeny backbone↗
GoaTGenomes on a Tree · Sangergenome & karyotype↗
NCBIUS National Library of Medicinegenome & karyotype↗
Tree of SexTree of Sex Consortiumgenome & karyotype↗
Paleobiology DatabasePBDB consortiumfossil record↗
WikidataWikimedia Foundationstructured facts↗Every layer below draws on the sources above — open one to explore it, or use ← → to move between tabs.
The San Bernardino kangaroo rat (Dipodomys merriami parvus) is a species of rodent in the family Heteromyidae. It is one of 19 recognized subspecies of Merriam's kangaroo rat (Dipodomys merriami) that are spread throughout the arid regions of the southwestern United States and Mexico. Like Dipodomys merriami, the San Bernardino kangaroo rat has the diagnostic trait of having four toes on its hind legs. Additionally, because of its geographic isolation, it has become the most highly differentiated subspecies of D. merriami.
No narrative description available for this taxon yet.
Size & morphology4
Life cycle & reproduction9
Diet & foraging6
Habitat & environment1
Physiology & chemistry4
Other traits5
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 Dipodomys merriami has left across the world's sequence archives.
At a glance
★ 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.
Besides the big genome in the nucleus, cells carry a small, circular loop of DNA inside the cell's energy factories — the mitochondria. It is inherited almost only from the mother and is a leftover from ancient bacteria that moved into the cell. The mitochondrial markers above (ND*, COX, CYTB…) are read from exactly this loop. Outer ring = one strand, inner ring = the other.
The complete instruction manual Dipodomys merriami 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
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).
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
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 solid bar is the fossil range: the span between the oldest and the youngest fossil that palaeontologists have assigned to Dipodomys merriami. Above itBeside it, each dot is one dated fossil find — few enough to count, so they are drawn individually rather than as a graph. 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. Where the DNA reaches further back than the oldest fossil, the gap is hatched: the ghost lineage. It means the lineage was already out there, but has left us nothing we have dug up yet.
How it livedPBDB
Record type13 733 records
Origin
Range
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
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.
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Holding institutions35 of 70 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
| Institution | Specimens |
|---|---|
| Tempe, US | 2 385 |
| München, DE | 1 857 |
| Zacatecas, MX | 1 599 |
| Provo, US | 1 152 |
| ASUlocation not on record | 779 |
| Seattle, US | 640 |
| EL PASO, US | 474 |
| Sam Noble Oklahoma Museum of Natural Historylocation not on record | 437 |
| San Diego, US | 410 |
| New Mexico Museum of Natural History and Sciencelocation not on record | 406 |
| ASNHClocation not on record | 315 |
| Ann Arbor, US | 200 |
| Louisiana State University, Museum of Zoologylocation not on record | 199 |
| Fort Hays State University, Sternberg Museumlocation not on record | 146 |
| Wuzhou, CN | 127 |
| Berkeley, US | 102 |
| CASlocation not on record | 100 |
| University of Nevada, Museum of Biologylocation not on record | 75 |
| Washington, US | 60 |
| Cambridge, US | 57 |
| La Paz, MX | 50 |
| San Nicolás de los Garza, MX | 45 |
| Natural History Museum of Utahlocation not on record | 41 |
| Mongolian Museum of Natural Historylocation not on record | 37 |
| Texas Cooperative Wildlife Collectionlocation not on record | 36 |
| Moore Laboratory of Zoology, Occidental Collegelocation not on record | 34 |
| Ithaca, US | 32 |
| Tacoma, US | 32 |
| Bonn, DE | 31 |
| Mexico City, MX | 30 |
| Washington State University, Charles R. Conner Museumlocation not on record | 29 |
| Chicago, US | 23 |
| Facultad de Ciencias Marinas, Universidad Autónoma de Baja Californialocation not on record | 20 |
| Toronto, CA | 19 |
| Centro de Investigaciones Biologicas del Noroeste S. C.location not on record | 19 |
| Museo civico La Terra e l'Uomo di Crocetta del Montellolocation not on record | 17 |
| North Carolina Museum of Natural Scienceslocation not on record | 17 |
| East Lansing, US | 15 |
| Philip L. Wright Zoological Museumlocation not on record | 14 |
| Abilene Christian University Natural History Collectionlocation not on record | 11 |
| Ciudad de México, MX | 9 |
| University of Wyoming Museum of Vertebrateslocation not on record | 9 |
| Geneva, CH | 9 |
| Ohio State University - Mammal Division, Columbus, OH (OSUM)location not on record | 9 |
| South Kensington, GB | 8 |
| Mexico City, MX | 8 |
| California State University, Long Beachlocation not on record | 8 |
| 7 | |
| New Haven, US | 7 |
| Florida Museum of Natural History- Zoology, Paleontology & Paleobotanylocation not on record | 7 |
| San Francisco, US | 7 |
| Indiana State Universitylocation not on record | 6 |
| Instituto de Ecología, Universidad Nacional Autónoma de Méxicolocation not on record | 5 |
| Chicago, US | 4 |
| Santa Cruz, US | 4 |
| Edmonton, CA | 4 |
| Iowa City, US | 4 |
| University of Wisconsin-Stevens Pointlocation not on record | 3 |
| The College of Idaho, Orma J. Smith Museum of Natural Historylocation not on record | 3 |
| University of California Los Angeleslocation not on record | 2 |
| Ciudad Juárez, MX | 2 |
| Central Michigan University Museum of Cultural and Natural Historylocation not on record | 1 |
| San Luis Potosí, MX | 1 |
| Helsinki, FI | 1 |
| University of Wisconsin, Zoological Museumlocation not on record | 1 |
| Hardin-Simmons Universitylocation not on record | 1 |
| Manitoba Museumlocation not on record | 1 |
| Chongqing Museumlocation not on record | 1 |
| California State Universitylocation not on record | 1 |
| UTCMlocation not on record | 1 |
Where the DNA of Dipodomys merriami 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
Where its DNA was found
How strong is each trace?
Modelled climatemodelled
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.