Data from: No evidence for the melanin desiccation hypothesis in a larval Lepidopteran
Data files
Oct 21, 2024 version files 32.11 KB
-
Desiccation_Data_F22.csv
11.67 KB
-
Desiccation_Photo_Data_F23.csv
11.19 KB
-
README.md
3.51 KB
-
Vapometer_Data_S24.csv
5.74 KB
Abstract
Water regulation is an important physiological challenge for insects due to their small body sizes and large surface area to volume ratios. Adaptations for decreasing cuticular water loss, the largest avenue of loss, are especially important. The melanin desiccation hypothesis states that melanin molecules in the cuticle may help prevent water loss, thus offering protection from desiccation. This hypothesis has much empirical support in Drosophila species, but remains mostly untested in other taxa, including Lepidoptera. Because melanin has many other important functions in insects, its potential role in desiccation prevention is not always clear. In this study we investigated the role of melanin in desiccation prevention in the white-lined Sphinx moth, Hyles lineata (Lepidoptera, Sphingidae), which shows high plasticity in the degree of melanin pigmentation during the late larval instars. We took advantage of this plasticity and used density treatments to induce a wide range of cuticular melanization; solitary conditions induced low melanin pigmentation while crowded conditions induced high melanin pigmentation. We tested whether more melanic larvae from the crowded treatment were better protected from desiccation in three relevant responses: i) total water loss over a desiccation period, ii) change in hemolymph osmolality over a desiccation period, and iii) evaporation rate of water through the cuticle. We did not find support for the melanin desiccation hypothesis in this species. Although treatment influenced total water loss, this effect did not occur via degree of melanization. Interestingly, this implies that crowding, which was used to induce high melanin phenotypes, may have other physiological effects that influence water regulation. There were no differences between treatments in cuticular evaporative water loss or change in hemolymph osmolality. However, we conclude that osmolality may not sufficiently reflect water loss in this case. This study emphasizes the context dependency of melanin’s role in desiccation prevention and the importance of considering how it may vary across taxa. In lepidopteran larvae that are constantly feeding phytophagous insects with soft cuticles, melanin may not be necessary for preventing cuticular water loss.
README: No evidence for the melanin desiccation hypothesis in a larval Lepidopteran
Sarah Britton and Goggy Davidowitz
Description of data
The data can be found in three files.
"Desiccation_Data_F22.csv"
This file contains the raw for the primary experiment that was conducted (where we measured total water loss and change in osmolality). Below is a description of the variables.
- ID = Individual larval ID numver
- Devo_Day = Day of development when measurement was taken for that individual (Day 0 = day egg was laid). All larvae were in 5th isntar.
- Treatment = From crowded (C) or solitary (S) experimental treatment
- Treatment_Binary = Converted to binary for path analysis. Crowded = 0, Solitary = 1
- Day in = Date of measurements
- Chamber_Humidity = humidity range in chamber
- Avg_Temp = avereage temperature in chamber in degrees C
- before_mass = larval mass before going in chamber (grams)
- before_mass_mg = mass in mg
- SA = surface area in mm^3
- after_mass = larval mass after desiccation in chamber (grams)
- frass_mass = mass of frass (if any) found in cup (grams)
- delta_mass = after mass - initial mass
- percent_mass_change = (after mass - initial mass)/ initial mass
- before_osmo = osmolality before going into chamber
- after_osmo = osmolality after desiccaton chamber
- delta_osmo = after - before osmolality
Note that only a subset of individuals was used for osmolality measurements so the osmolality columns (before_osmo*, *after_osmo, and delta_osmo) will have empty cells.
Osmolality measurements were taken for a subset of individuals so some individuals do not have values in the osmolality columns.
"Desiccation_Photo_Data_F23"
This file contains the ImageJ data used to quantify melanin. Variables with "gray" represent gray values while variables with "percent" represent percentage of melanic pixels. R, G, and B refer to the red, green, and blue channels of the multispectral image. While all data are included here, note that we only used date from the green channel. Thus, the two variables of interest are "darkness_G" and "percent_G." Darkness was calculated as 29-gray value (see text for explanation)
"Vapometer_Data_S24"
This file contains data from the second experiment where we measured evaporative water loss across the cuticle. Below is a description of the variables.
- larval_ID = Individual larval ID number
- Treatment = From crowded or solitary experimental treatment
- Treatment_Binary = Converted to binary for path analysis. Crowded = 0, Solitary = 1
- date = Date of measurements
- ambient_temp = temperature in room during measurements in degrees C
- ambient_humidity = humidity in room during measurements
- mass = larval mass in grams
- body_temp = larval body temperature in degrees C
- reading_1...reading_8 = replicate readings from vapometer (g/m^2/hour)
- avg_reading = average of all vapometer readings (g/m^2/hour)
- readings_stdev = stadard deviation of readings (g/m^2/hour)
- range = range of readings (g/m^2/hour)
- coef_var = coefficient of variation for readings
The ImageJ data for this dataset can be described the same way as above.
Note that most individuals had 7 vapometer readings, but a few had 6 or 8 readings. Thus, there are some empty cells. The average reading was taken for all available readings.
Description of Code
All statistical analyses were conducted in R. The R file "Hyles_desiccation" can be used to replicate all analyses with the above data files.