T1 · longitudinal recovery
Recovered along B0. At one T1: 63%.
Explore what the signal does, how scan timing changes an image, and why blood oxygenation can reveal changes associated with brain activity.
Start just after a 90° RF pulse. T1 describes recovery along the main field. T2 describes loss of transverse coherence. T2* includes additional dephasing from magnetic-field differences.
Recovered along B0. At one T1: 63%.
Transverse signal remaining. At one T2: 37%.
Phase arrows are schematic; percentages and curves follow the exponential model. Graphs use different time ranges. Dashed vertical lines mark your selected time when it is in range. In the last graph, dashed orange is T2 and solid purple is T2*.
Shorten T2′: T2* falls faster. Lengthen T2′: T2* approaches T2. T1 recovery happens simultaneously. These controls are independent mathematical parameters; not every combination describes a real tissue.
TR is the interval between excitation pulses. TE is the time from excitation to the measured echo. Keep tissue constants fixed and change the scanner's timing.
Timing schematic; spacing is not to scale. Gradient echo uses gradient reversal, without a 180° RF refocusing pulse.
A schematic, not a patient scan. A fixed brightness scale makes overall signal loss visible.
The recovery term sets the magnetization available for excitation. The decay term sets how much transverse signal survives to TE. Longer TR reduces T1 saturation; longer TE increases transverse-decay sensitivity while reducing signal.
Illustrative constants in ms: white matter T1 800, T2 90, T2* 45; gray matter 1300, 100, 50; fluid 4000, 2000, 1000. Equal proton density isolates relaxation. Real values depend on tissue and field strength.
The model assumes repeated 90° excitation with ideal spoiled recovery. The gradient-echo option substitutes T2* to isolate its effect; real gradient-echo signals also depend on flip angle and sequence details. Presets illustrate contrast, not scanner protocols.
BOLD means blood-oxygen-level dependent. It measures a vascular response associated with neural activity, rather than recording neurons firing directly.
An illustrative single-event response, delayed peak and small undershoot. Shape and delay vary across people and regions.
Cell colors illustrate the mechanism; counts are not physiological measurements.
Longer TE increases modeled BOLD percentage sensitivity, but baseline signal decays more. Shorter TR adds samples; it does not remove the vascular delay.
The scanner repeats a T2*-sensitive acquisition, often gradient-echo echo-planar imaging, to collect a time series at each voxel. Researchers model task timing with a hemodynamic response, account for motion and other confounds, and estimate task-related responses. Statistical maps are commonly overlaid on an anatomical scan.
This model fixes baseline T2* at 40 ms and illustrates a change in R2* = 1/T2*. TE affects exp(−TE × R2*). Here TR controls sampling only; saturation, noise and physiological variability are omitted. BOLD reflects neural–vascular coupling, not a unique measure of firing rate.
Gradients make frequency and phase depend on position. Columns have different frequencies; rows have different starting phases. The receiver measures their sum. Many encoding measurements and an inverse Fourier transform reconstruct the image.
Each k-space measurement mixes contributions across many positions. One k-space point is not one voxel.