| AT_P_283 | Storage 56 days | Primary dormancy was measured as the progressive increase of germination rate measured after 56 days of dry storage | continuous | 110 |
| AT_P_282 | Storage 28 days | Primary dormancy was measured as the progressive increase of germination rate measured after 28 days of dry storage | continuous | 110 |
| AT_P_281 | Storage 7 days | Primary dormancy was measured as the progressive increase of germination rate measured after 7 days of dry storage | continuous | 110 |
| AT_P_280 | Seed bank 133-91 | Genotypes consistently decreased their percentage of germination between 91 and 133 days of dry storage. The time point for this sudden reduction in germination rate was scored by the slope between germination percentages at these two time points | continuous | 110 |
| AT_P_28 | As75 | Arsenic concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_279 | DSDS50 | Number of days of seed dry storage required to reach 50% germination, or DSDS50 value (Alonso-Blanco et al., 2003) | continuous | 109 |
| AT_P_278 | Germ in dark | The ability to germinate in the dark at 4°C was measured as the percentage of non dormant seeds that can germinate during 1-week long cold exposure, in the absence of light | continuous | 93 |
| AT_P_277 | Secondary Dormancy | Secondary dormancy was given by the slope between the germination percentages of non-dormant seeds after one and six weeks of cold treatment. Viability of non germinating seeds after cold treatment was confirmed as described in Cadman et al., 2006 | continuous | 93 |
| AT_P_274 | After Vern Growth | Vegetative growth rate after vernalization was estimated as the increment of cm2 leaf area per day between each of the three time points for which leaf area was measured | continuous | 110 |
| AT_P_273 | Vern Growth | Vegetative growth rate during vernalization was estimated as the increment of cm2 leaf area per day between each of the three time points for which leaf area was measured | continuous | 110 |
| AT_P_27 | Zn66 | Zinc concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_26 | Cu65 | Copper concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_25 | Ni60 | Nickel concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_24 | Co59 | Cobalt concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_23 | Fe56 | Iron concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_22 | Mn55 | Manganese concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_21 | Ca43 | Calcium concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_20 | K39 | Potassium concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_2 | LDV | Number of days following stratification to opening of first flower. The experiment was stopped at 200 d, and accessions that had not flowered at that point were assigned a value of 200 | continuous | 168 |
| AT_P_19 | S34 | Sulfur concentrations in leaves, grown in soil. Elemental analysis was performed with an ICP-MS (PerkinElmer). Sample normalized to calculated weights as described in Baxter et al., 2008 | continuous | 93 |
| AT_P_186 | Bacterial titer | Following inoculation into leaf tissues, the titers of bacteria were measured at 0 and 4 days. Bacterial titres were measured from hole-punched leaf disks ground in 200μL of 10 mM MgSO4. Measurements were expressed as colony forming units per unit area and replicated in triplicate. | continuous | 95 |
| AT_P_185 | Aphid number | On day 25 of growth,two alate females of the common peach aphid, Myzus persicae,were placed on each of four plants of each of the 96 genotypes. Nine days later, the number of offspring produced by these aphids on each plant was recorded. | continuous | 94 |
| AT_P_184 | Trichome avg JA | Measurements were collected from leaf disks removed from the 11th leaf of plants that had been treated with 0.6 ml of a 0.45mM solution of jasmonic acid (Sigma J-2500) in water (JA). Trichome density was calculated as the trichome number per disk divided by the disk area | continuous | 94 |
| AT_P_183 | Trichome avg C | Measurements were collected from leaf disks removed from the 11th leaf of plants that had been treated with 0.6ml of a water control (C). Trichome density was calculated as the trichome number per disk divided by the disk area | continuous | 94 |
| AT_P_182 | Hypocotyl length | After seven days growth under the photocycle and thermocycle treatment,plants were flattened directly on the agar and imaged on a flatbed scanner. Hypocotyl lengths were determined using NIH Image | continuous | 89 |
