Data from: Garden, greenhouse, or climate chamber? Experimental conditions influence whether genetic differences are phenotypically expressed
Data files
Jun 03, 2026 version files 14.43 MB
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Biomass_Stem_Data.xlsx
31.16 KB
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Flowering_Data.xlsx
23.81 KB
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Light_intensity_Data.xlsx
9.08 KB
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Maastricht_Climate_Data.xlsx
8.74 MB
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PAR_Data.xlsx
13.96 KB
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README.md
4.76 KB
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SLA__SPAD_RosetteDiameter_Data.xlsx
38.47 KB
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Soil_Temperature_Moisture_Data.xlsx
5.48 MB
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Weather_Garden_Data.xlsx
88.71 KB
Abstract
Common-environment experiments are important to study genetically based phenotypic variation within and among plant populations. Such experiments can be performed in an experimental garden, greenhouse, or climate chamber. However, phenotypic expression may be strongly affected by the environmental conditions and influenced by parental and storage effects. In particular, when the expression of genetically based phenotypic variation depends on the environment (G 9 E interaction), it can strongly influence conclusions. In this study, we assessed the effects of three different growth facilities – outdoor garden, greenhouse, and climate chamber – on phenotypic expression. We compared ancestral and descendant genotypes of the same population of Leontodon hispidus. We further evaluated differences in phenotypic expression between plants grown after one (F1) vs. two (F2) intermediate generations. As expected, we observed strong differences among plants growing in different environments (i.e., facilities). More importantly, we found that descendants had larger rosettes than ancestors only in the greenhouse, and they flowered later than ancestors exclusively in the climate chamber, indicating G 9 E interactions. We did not find significant differences between different intermediate generations within the growth facilities. Overall, our study demonstrates that environmental variation among growth facilities can determine both the presence and magnitude of phenotypic differences. Consequently, differences observed in certain experimental settings may be overestimated compared with expression under natural conditions. Concluding, we recommend combining greenhouse and growth chamber resurrection experiments with field experiments to obtain a more comprehensive understanding of evolutionary changes.
https://doi.org/10.5061/dryad.qz612jmx5
This is the raw data from a study, where we assessed the effects of three different growth facilities – outdoor garden, greenhouse, and climate chamber –, on phenotypic expression. We compared ancestral and descendant genotypes of the same population of Leontodon hispidus. We further evaluated differences in phenotypic expression between plants grown after one (F1) vs. two (F2) intermediate generations.
The final design consisted of 360 plants (3 growth facilities × 2 temporal origins × 2 generations × 7/8 maternal lines × 4 replicates) which were distributed among three facilities: outdoor garden, greenhouse, and climate chamber. All plants were grown in 1.5 L pots and monitored continuously for temperature, soil moisture, and light intensity (DLI) using TMS-4 loggers and light meters. This design allowed for the comparison of phenotypic expression across distinct environmental treatments and temporal origins.
File list
- Maastricht_Climate_Data.xlsx
- Light_intensity_Data.xlsx
- Weather_Garden_Data.xlsx
- PAR_Data.xlsx
- Flowering_Data.xlsx
- SLA__SPAD_RosetteDiameter_Data.xlsx
- Biomass_Stem_Data.xlsx
- Soil_Temperature_Moisture_Data.xlsx
Description of the data and file structure
- Maastricht_Climate_Data.xlsx: Climate data from the weather station in Maastricht, located 14 km from the L. hispidus population. Given are Year, Month, Day, Avg_T (average daily temperature in °C), Max_T (max daily temperature in °C), Precip (daily precipitation in mm)
- Light_intensity_Data.xlsx: At the start of the experiment at noon, we measured the light intensity using a light meter (Panlux electronic 2, GMC-Instruments, Nürnberg, Germany) in each growth facility at 12 spatially distributed pots at the same height, 2 cm above the soil. Given are Env (growth facility, GH = Greenhouse, OD = Outdoor Garden, CC = Climate Chamber) and LightIntensity[klx]
- Weather_Garden_Data.xlsx: After the end of the experiment, hourly solar radiation data (Wm-2) was extracted for the whole experimental period from a weather station in the outdoor garden (iMetos 1, Pessl Instruments GmbH, Weiz, Austria). Given are Time (measured every 30 min) and SolarRadiation[W/m²]
- PAR_Data.xlsx: For the climate chamber, we directly measured Photosynthetic Active Radiation (PAR) at 12 spatially distributed spots at pot height using a PAR sensor (PAR Special sensor SKP 210, Skye Instruments Ltd, Powys, UK). Given are Env (growth facility, CC = Climate Chamber) and PAR[ymol/s*m²] (Photosynthetic Active Radiation).
- Flowering_Data.xlsx: Recording of the initial size (rosette diameter) at the start of the experiment and flowering date. Sowing date was 31.05.2022. Given are origin (Descendants, Ancestors), seed family (i.e., maternal line), Gen (F1 = one intermediate generation, F2 = two intermediate generations), Rep (Replicate), Env (growth facility, GH = Greenhouse, OD = Outdoor Garden, CC = Climate Chamber), FT (Flowering Time) and Initialsize (rosette diameter at the start of the experiment in cm)
- SLA_SPAD_RosetteDiameter_Data.xlsx: recording of the rosette diameter and leaf traits at the end of the experiment. Given are origin (Descendants, Ancestors), seed family (i.e., maternal line), Gen (F1 = one intermediate generation, F2 = two intermediate generations), Rep (Replicate), Env (growth facility, GH = Greenhouse, OD = Outdoor Garden, CC = Climate Chamber), RosetteDiameter[cm] (diameter of the rosette in cm)m spad1 - spad4 (four respective SPAD measurements), Area[cm2] (area of the selected leaf in cm²), Freshmg (fresh weight of the selected leaf in mg), Drymg (weight of the selected leaf after drying in mg)
- Biomass_Stem_Data.xlsx: recording of the vegetative biomass (rosette), reproductive biomass (stems and flowers), and number of stems. Given are origin (Descendants, Ancestors), seed family (i.e., maternal line), Gen (F1 = one intermediate generation, F2 = two intermediate generations), Rep (Replicate), Env (growth facility, GH = Greenhouse, OD = Outdoor Garden, CC = Climate Chamber), vegbiomass (weight of rosette in g), repbiomass (weight of stems and flowers in g), stem number (number of stems)
- Soil_Temperature_Moisture_Data.xlsx: Recordings of the Temperature and Soil moisture data during the experiment from 4 TMS-4 loggers placed in random pots for each facility. Given are Time, T1 (Soil Temperature in °C), T2 (Soil Surface Temperature in °C), T3 (Air Temperature in °C), and SM (Soil Moisture Count, the unit provided by the TMS-4 logger)
