Data and code for: Acute heat priming promotes short-term climate resilience of early life stages in a model sea anemone
Data files
Nov 16, 2023 version files 792.77 KB
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Development_data.csv
3.65 KB
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Development_data.xlsx
15.94 KB
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DRC_data.csv
5.62 KB
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DRC_data.xlsx
19.48 KB
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HSP70_data.csv
739 B
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HSP70_data.xlsx
10.24 KB
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Long_term_growth_data.csv
116.16 KB
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Long_term_growth_data.xlsx
194.28 KB
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Long_term_heattol_data.csv
283 B
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Long_term_heattol_data.xlsx
9.75 KB
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LT50_data.csv
668 B
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LT50_data.xlsx
9.81 KB
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README.md
6.98 KB
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Respiration_and_protein_data.csv
3.12 KB
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Respiration_and_protein_data.xlsx
13.33 KB
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Size_data.csv
156.20 KB
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Size_data.xlsx
226.52 KB
Abstract
Across diverse taxa, sublethal exposure to abiotic stressors early in life can lead to benefits such as increased stress tolerance upon repeat exposure. This phenomenon, known as hormetic priming, is largely unexplored in early life stages of marine invertebrates, which are increasingly threatened by anthropogenic climate change. To investigate this phenomenon, larvae of the sea anemone and model marine invertebrate Nematostella vectensis were exposed to control (18°C) or elevated (24°C, 30°C, 35°C, or 39°C) temperatures for 1 hour at 3 days post-fertilization (DPF), followed by return to control temperatures (18°C). The animals were then assessed for growth, development, metabolic rates, and heat tolerance at 4, 7, and 11 DPF. Priming at intermediately elevated temperatures (24°C, 30°C, or 35°C) augmented growth and development compared to controls or priming at 39°C. Indeed, priming at 39°C hampered developmental progression, with around 40% of larvae still in the planula stage at 11 DPF, in contrast to 0% for all other groups. Total protein content, a proxy for biomass, and respiration rates were not significantly affected by priming, suggesting metabolic resilience. Heat tolerance was quantified with acute heat stress exposures, and was significantly higher for animals primed at intermediate temperatures (24°C, 30°C, or 35°C) compared to controls or those primed at 39°C at all time points. To investigate a possible molecular mechanism for observed changes in heat tolerance, the expression of heat shock protein 70 (HSP70) was quantified at 11 DPF. Expression of HSP70 significantly increased with increasing priming temperature, with the presence of a doublet band for larvae primed at 39°C, suggesting persistent negative effects of priming on protein homeostasis. Interestingly, primed larvae in a second cohort cultured to 6 weeks post-fertilization continued to display hormetic growth responses, whereas benefits for heat tolerance were lost; in contrast, negative effects of short-term exposure to extreme heat stress (39°C) persisted. These results demonstrate that some dose-dependent effects of priming waned over time while others persisted, resulting in heterogeneity in organismal performance across ontogeny following priming. Overall, these findings suggest that heat priming may augment the climate resilience of marine invertebrate early life stages via the modulation of key developmental and physiological phenotypes, while also affirming the need to limit further anthropogenic ocean warming.
Dataset includes files for:
- Data pertaining to the development of Nematostella vectensis larvae past the planula stage
- Data pertaining to dose-response curves (DRC) quantifying survival of larvae after exposure to heat ramps
- Data pertaining to the expression of heat shock protein 70 (HSP70) in larvae at 11 days post-fertilization (DPF)
- Data pertaining to the long-term body column lengths and tentacles numbers of larvae and juveniles through 6 weeks post-fertilization (WPF)
- Data pertaining to the heat tolerance (survival) of juveniles at 6 WPF following heat shock
- Data pertaining to the lethal temperature 50s (LT50s) displayed by larvae derived from DRCs after heat shock
- Data pertaining to the respiration rates and protein content of larvae
- Data pertaining to the sizes of larvae from 4-11 DPF
Data and file structure
Files 1 and 2: Development_data.xlsx and .csv
These files are for data pertaining the development of Nematostella vectensis larvae past the planula stage
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- days post-fertilization = self-explanatory
- percent/planula count = percent/number of larvae in the planula stage
- percent/post-planula count = percent/number of larvae past the planula stage
Files 3 and 4: DRC_data.xlsx and .csv
These files are for data pertaining to dose-response curves (DRC) quantifying survival of larvae after exposure to heat ramps
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- days post-fertilization = self-explanatory
- treatment temperature (°C) = peak temperature to which larvae were exposed for 1 hour during a heat ramp
- larvae surviving = number of larvae alive 48 hours post-treatment
- total larvae = number of larvae originally treated
- proportion/percent surviving = larvae surviving/total larvae
Files 5 and 6: HSP70_data.xlsx and .csv
These files are for data pertaining to the expression of heat shock protein 70 (HSP70) in larvae at 11 days post-fertilization (DPF)
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- days post-fertilization = self-explanatory
- HSP70 = mean gray value for Western blot band representing HSP70 as determined via ImageJ
- tubulin = mean gray value for Western blot band representing tubulin as determined via ImageJ
- normalized HSP70 = HSP70/tubulin
- LT50 (°C) = lethal temperature 50 for larvae at 11 DPF, copied from LT50 data file
Files 7 and 8: Long_term_growth_data.xlsx and .csv
These files are for data pertaining to the long-term body column lengths and tentacles numbers of larvae and juveniles through 6 weeks post-fertilization (WPF)
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- weeks post-fertilization = self-explanatory
- body column length/width (cm/mm) = lengths and widths of larval/juvenile body columns as determined from images via ImageJ
- aspect ratio = length/width
- volume/surface area (mm^3/mm^2) = calculated from lengths and widths
- surface area to volume ratio = surface area/volume
- tentacles = number of tentacles possessed by juveniles
Files 9 and 10: Long_term_heattol_data.xlsx and .csv
These files are for data pertaining to the heat tolerance (survival) of juveniles at 6 WPF following heat shock
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- juveniles surviving = number of juveniles surviving at 21 hours following heat shock
- total juveniles = number of juveniles originally exposed to heat shock
- survival (%) = juveniles surviving/total juveniles*100
Files 11 and 12: LT50_data.xlsx and .csv
These files are for data pertaining to the lethal temperature 50s (LT50s) displayed by larvae derived from DRCs after heat shock
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- days post-fertilization = self-explanatory
- LT50 (°C) = lethal temperature as determined from dose-response curves of survival following acute heat shock
Files 13 and 14: Respiration_and_protein_data.xlsx and .csv
These files are for data pertaining to the respiration rates and protein content of larvae
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- days post-fertilization = self-explanatory
- respiration (nmol O2 per minute) = respiration rate determined by taking the slope of raw data from respirometer
- number of larvae = number of larvae in well of respirometry plate
- respiration (nmol O2 per minute per larva) = respiration (nmol O2 per minute)/number of larvae
- protein (ug) = protein content of larvae in well as determined via Bradford assays
- protein (ug per larva) = protein (ug)/number of larvae
- respiration (nmol O2 per minute per protein) = respiration (nmol O2 per minute per larva)/protein (ug)
- respiration (pmol O2 per minute per protein) = respiration (nmol O2 per minute per protein)*1000
Files 15 and 16: Size_data.xlsx and .csv
These files are for data pertaining to the sizes of larvae from 4-11 DPF
These files have headers, which include:
- priming temperature (°C) = temperature at which larvae were primed for 1 hour at 3 DPF
- group = arbitrary number assigned to the replicate dishes in which larvae were cultured
- weeks post-fertilization = self-explanatory
- body column length/width (cm/mm) = lengths and widths of larval body columns as determined from images via ImageJ
- aspect ratio = length/width
- volume/surface area (mm^3/mm^2) = calculated from lengths and widths
- surface area to volume ratio = surface area/volume
Code/Software
Filse 1 and 2: Nematostella HP script for manuscript.R
These files are an R script (markdown and PDF forms) that was used to analyze and generate plots of data, and can be run using the .csv files.
All details are present in the manuscript and code comments.