Number of distinct genome duplication events early in vertebrate evolution
|
Vertebrates |
2 |
genome duplication events |
116989 |
Dehal P, Boore JL. Two... |
Photon yield of Oxygen evolution on basis of absorbed light in ferns
|
Various |
0.102 (±0.006 Table - link) |
Oxygen molecules/photon |
104652 |
Björkman O. & Demmig... |
Estimated ancestral selenoproteome size and atmospheric O2 concentration during vertebrate evolution
|
Vertebrates |
Table - link |
N/A |
104533 |
Castellano S et al Low... |
Population splits and effective population sizes (Ne) during great ape evolution
|
Apes |
Figure - link |
N/A |
111515 |
Prado-Martinez J et al.... |
Photon yield of Oxygen evolution on basis of absorbed light in C3 plants
|
Various |
0.106 (±0.001 Table - link) |
Oxygen molecules/photon |
104653 |
Björkman O. & Demmig... |
Photon yield of Oxygen evolution on basis of incident light in C3 plants
|
Various |
0.0891 (±0.0009) |
Oxygen molecules/photon |
104657 |
Björkman O. & Demmig... |
Conquest of dry land by vertebrate animals (the evolution of the first four-legged, amphibious animals) & origin of amniotes
|
vertebrates |
conquest of dry land ~360Mya: origin of amniotes ~310Mya |
Mya |
113179 |
Sander PM. Paleontology.... |
Factor by which rate of evolution of the mitochondrial genome appears to exceed that of the single-copy fraction of the nuclear genome
|
Primates |
~10 |
unitless |
113082 |
Brown WM, George M Jr... |
Time when the metazoan toolkit of conserved functional components and processes first arised in evolution
|
Metazoa animals |
Table - link |
years ago |
117011 |
Gerhart J, Kirschner... |
Estimated time range of evolution of rise to dominance of C4 plants in grasslands
|
Plants |
5-8 |
Mya |
105195 |
Christin PA, Besnard G... |
Leaf absorptance, photon yield for 0xygen evolution on the basis of incident and absorbed photons and chlorophyll fluorescence characteristics for 44 plants
|
Various |
Table - link |
N/A |
104650 |
Björkman O. & Demmig... |
The characteristic time for new mutations to drift to high frequency under neutral evolution in the human population
|
Human Homo sapiens |
~1e+6 |
years |
110201 |
Sabeti PC, Schaffner SF... |
Comparison among taxonomic groups and life forms of the photon yield of O2 evolution, leaf absorptance and variable to maximum fluorescence in leaves and fronds of C3 species
|
Various |
Table - link |
N/A |
104651 |
Björkman O. & Demmig... |
Biomass formation rate and the specific rates of glucose uptake, carbon dioxide evolution, oxygen uptake, acetate formation and ammonium uptake during steady-state growth
|
Bacteria Escherichia coli |
Table - link |
N/A |
113371 |
Kayser A, Weber J, Hecht V... |
Growth of E. coli and 14CO2 evolution during incubation with [U-14C]carbon source, each at 1 mM
|
Bacteria Escherichia coli |
Table - link |
N/A |
110836 |
Shearer G, Lee JC, Koo JA... |
Summary of the kinetic parameters of net 02 evolution, net HCO2 transport, and gross CO2 transport during steady-state photosynthesis
|
Cyanobacteria Synechococcus PCC7002 |
Table - link |
N/A |
110475 |
Sultemeyer D, Price GD... |
test11111
|
test |
100 (Table - link) |
Min |
109313 |
Shaner NC, Steinbach PA... |
A timeline showing OMZ (oxygen minimum zone) chemistry, the relative contributions from different primary producers, and the evolution of eukaryotic heterotrophs
|
Biosphere |
Figure - link |
Mya |
110483 |
Johnston DT, Wolfe-Simon F... |
Maturation time of mPlum fluorescent protein in the Burkitt lymphoma Ramos, a human B cell line
|
Human Homo sapiens |
100 (Table - link) |
Min |
106878 |
Shaner NC, Steinbach PA... |
Growth parameters for ancestral and evolved LTEE isolates
|
Bacteria Escherichia coli |
Table - link |
N/A |
109375 |
Harcombe WR, Delaney NF... |