Harvard Forest

Data Archive

HF062

Canopy Chemistry Study at Harvard Forest 1992

Related Publications

Data

• hf062-01: plot data (preview)
• hf062-02: tree data (preview)

Overview

• Lead: Mary Martin, John Aber
• Investigators:
• Contact: Information Manager
• Start date: 1992
• End date: 1992
• Status: complete
• Location: Harvard Forest
• Latitude: +42.45 to +42.55 degrees
• Longitude: -72.23 to -72.16 degrees
• Elevation: 205 to 420 meter
• Datum: WGS84
• Taxa:
• Release date: 2023
• Language: English
• EML file: knb-lter-hfr.62.19
• DOI: digital object identifier
• EDI: data package
• DataONE: data package
• Related links:
• Study type: short-term measurement
• Research topic: physiological ecology, population dynamics and species interactions
• LTER core area: primary production, mineral cycling
• Keywords: canopies, cellulose, nitrogen, remote sensing
• Abstract:

  As part of NASA's Accelerated Canopy Chemistry Program (ACCP) analyses were performed for the determination of carbon constituents and nitrogen content in fresh forest foliage. Samples were analyzed using a series of extraction's that yielded different carbon constituents: non-polar, polar, cellulose and lignin. Nitrogen analyses were conducted using a standard combustion procedure. Approximately 1000 leaf samples were collected from 5 geographically distinct sites and were analyzed at the University of New Hampshire to ensure consistency in analysis. Results were used as a calibration set for Visible/NIR reflectance and the estimation of carbon and nitrogen concentrations at both the leaf and canopy level. The canopy level study uses high spectral resolution data from NASA's Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) to estimate canopy level nitrogen and lignin concentration for the Harvard Forest and other study areas.

  The current link to this data from the Harvard Forest LTER site is to an archive at the University of New Hampshire. Additional information on this study, including, leaf level spectra and remote sensing data are available from a NASA DAAC site (http://www-eosdis.ornl.gov/daacpages/accp.html). Additional foliar chemistry data is also available on a searchable on-line database at http://www.folchem.sr.unh.edu.

• Methods:

  Sample preparation

  Prior to analysis, samples were oven dried at 70 degrees C for 48 hours, ground to 20-mesh and homogenised.

  Proximate carbon fraction analysis

  Carbon constituent analyses were performed using a series of extraction's modified from those used by Ryan, et. al. Two grams of material were refluxed with 75 ml of dichloromethane for five hours to remove the non-polar component of the sample (fats, waxes, and other organic soluble materials) using a block digestor and condenser apparatus modified from a TAPPI procedure. Polar extractives such as phenols, simple sugars, starch and simple amino acids were removed by boiling a subsample (1.6 g) of tissue from the non-polar analysis for three hours in deionised water and then filtering. Sample size was increased from the recommended 0.5 g to 1.6 g to ensure sufficient post polar sample quantity for the acid digestion. Lignin and cellulose content were determined by a modified wood-products chemistry procedure. A 0.5 g subsample of post polar material was digested in 72% sulphuric acid for 1 hour in a 30 degree C water bath. This was then diluted with water until a 28:1 water to acid ratio was formed to carry out secondary hydrolysis while boiling for 4 hours. To wet the sample thoroughly we used 1.5 ml of acid for each 100 mg of sample, a 0.5 ml increase in acid over the quantity Effland recommended. At the end of this process the sample was filtered. Residual tissue was considered lignin and mass lost during digestion was considered cellulose. The percentages of the different constituents were determined gravimetrically. Oven-dried samples were temporarily stored in dessicators to prevent gaining moisture from the atmosphere before weighing.

  Calculations for carbon chemistry

  % non polar = (Pre non polar mass - post non polar mass)/ pre non polar mass; % polar = ((pre polar mass - post polar mass)/ pre polar mass) * (1-% non polar); % cellulose = ((pre digest mass - post digest mass)/ pre digest mass) * (1- % non polar - % polar); and % lignin = (post digest mass / pre digest mass) * (1- % non polar- % polar).

  Nitrogen analyses

  Nitrogen determination was performed using a Perkin-Elmer 2400 CHN Elemental Analyser. The CHN analyser combusts a sample to convert elements to gases (CO2, H2O, N2). The resulting data are weight percentage of carbon, hydrogen and nitrogen (CHN). In addition, a total Kjeldahl nitrogen (TKN) determination was performed on a subset of 100 samples. This method uses sulphuric acid and a digestion catalyst of potassium sulphate, cupric sulphate and selenium powder on ground leaf samples to generate a liquid sample for colorimetric analysis, and was included as a alternate method of nitrogen determination included for QA/QC as assessment. In addition, three replicate samples of each of the three standard materials were sent to Oregon State University for a similar Kjeldahl analysis. Finally, three National Bureau of Standards (NBS) 1.2% nitrogen pine foliage standards were included in each of four Kjeldhal runs.

  Analysis Methods

  Method ID: 1 Name: Near Infrared Spectroscopy. Description: Samples were dried at 70oC, and ground to pass a 1mm mesh screen. The dried and ground sample was scanned using a NIRSystems spectrophotometer. Foliar N, lignin and cellulose concentrations were predicted from the resulting spectral signatures. Citation: Bolster, K. L.; Martin, M. E., and Aber, J. A. 1996. Determination of carbon fraction and nitrogen concentration in tree foliage by near infrared reflectance: a comparison of statistical methods. Canadian Journal of Forest Research. 26(4):590-600.

  Method ID: 2. Name: ICP Analysis. Description: Digestate was analyzed for Al, Ca, Fe, K, Mg, Mn, P and Sr using an inductively coupled plasma spectrometer.

  Method ID: 3. Name: TKN digestion. Description: Samples were dried at 70oC, and ground to pass a 1mm mesh screen and digested using a modified TKN digestion using a selenium catalyst (Isaac and Johnson 1976). Citation: Isaac, R.A. and Johnson, W.C. 1976. Determination of total nitrogen in plant tissue using a block digestor. Journal of the AOAC 59: 98-100.

  Method ID: 4. Name: Microwave digestion. Description: Samples were dried at 70oC, and ground to pass a 1mm mesh screen. Dried and ground foliage was digested using a microwave assisted acid digestion procedure. Citation: 1996. EPA method 3052: Microwave assisted acid digestion of siliceous and organically based matrices. In Test methods for evaluating solid waste update (III). U.S. Environmental protection agency, Washington, DC.

  Method ID: 5. Name: TKN Analysis. Description: Analysis for the digestion of total foliar N was carried out using a Bran+Luebbe (Technicon) TRAACS 800 Autoanalyzer.

  Method ID: 6. Name: CHN Analysis

  Method ID: 7. Name: DCP Analysis. Description: Digestate was analyzed for Al, Ca, Fe, K, Mg, Mn, and P using a SpectraSpan III, ARL direct current plasma AES by Fisons Instruments Inc.. Citation: A.L. Page, R.H. Miller and D.R. Keeney (Eds), Methods of soil analysis chemical and microbiological properties, 2nd Edn, Vol. 2. America Society of Agronomy, Madison, WI (1982).

  Method ID: 8. Name: Dry Ash. Description: Foliage samples were dry ashed at 485 degrees C; taken up in 10% HCl. Citation: Munter, R.C. 1982. Current methods used by Research Analytical Laboratory University of Minnesota, St. Paul.

• Organization: Harvard Forest. 324 North Main Street, Petersham, MA 01366, USA. Phone (978) 724-3302. Fax (978) 724-3595.

• Project: The Harvard Forest Long-Term Ecological Research (LTER) program examines ecological dynamics in the New England region resulting from natural disturbances, environmental change, and human impacts. (ROR).

• Funding: National Science Foundation LTER grants: DEB-8811764, DEB-9411975, DEB-0080592, DEB-0620443, DEB-1237491, DEB-1832210.

• Use: This dataset is released to the public under Creative Commons CC0 1.0 (No Rights Reserved). Please keep the dataset creators informed of any plans to use the dataset. Consultation with the original investigators is strongly encouraged. Publications and data products that make use of the dataset should include proper acknowledgement.

• License: Creative Commons Zero v1.0 Universal (CC0-1.0)

• Citation: Martin M, Aber J. 2023. Canopy Chemistry Study at Harvard Forest 1992. Harvard Forest Data Archive: HF062 (v.19). Environmental Data Initiative: https://doi.org/10.6073/pasta/71974f4320029972668ba387d12940bb.

Detailed Metadata

hf062-01: plot data

1. plot: plot name
2. species: USDA Species ID code - look up at http://plants.usda.gov/
3. lat: latitude in decimal degrees (unit: degree / missing value: NA)
4. lon: longitude in decimal degrees with - to indicate W (unit: degree / missing value: NA)
5. elev: elevation of plot in meters (unit: meter / missing value: NA)
6. year: year
7. cellulose: percent cellulose (unit: dimensionless / missing value: NA)
8. lignin: percent lignin (unit: dimensionless / missing value: NA)
9. carbon: percent carbon (unit: dimensionless / missing value: NA)
10. hydrogen: percent hydrogen (unit: dimensionless / missing value: NA)
11. nitrogen: percent nitrogen (unit: dimensionless / missing value: NA)

hf062-02: tree data

1. plot: plot name
2. sample.id: Unique sample id. Usually a combination of date,site, plot, species, and tree
3. species: USDA Species ID code - look up at http://plants.usda.gov/
4. lat: latitude in decimal degrees (unit: degree / missing value: NA)
5. lon: longitude in decimal degrees with - to indicate W (unit: degree / missing value: NA)
6. elev: elevation of plot in meters (unit: meter / missing value: NA)
7. year: year
8. cellulose: percent cellulose (unit: dimensionless / missing value: NA)
9. cellulose.method: code for method used to digest and/or analyze samples (see method codes)
10. lignin: percent lignin (unit: dimensionless / missing value: NA)
11. lignin.method: code for method used to digest and/or analyze samples (see method codes)
    • 1: Near Infrared Spectroscopy
    • 2: ICP Analysis
    • 3: TNK digestion
    • 4: Microwave digestion
    • 5: TKN Analysis
    • 6: CHN Analysis
    • 7: DCP Analysis
    • 8: Dry Ash
12. carbon: percent carbon (unit: dimensionless / missing value: NA)
13. carbon.method: code for method used to digest and/or analyze samples (see method codes)
    • 1: Near Infrared Spectroscopy
    • 2: ICP Analysis
    • 3: TKN digestion
    • 4: Microwave digestion
    • 5: TKN Analysis
    • 6: CHN Analysis
    • 7: DCP Analysis
    • 8: Dry Ash
14. hydrogen: percent hydrogen (unit: dimensionless / missing value: NA)
15. hydrogen.method: code for method used to digest and/or analyze samples (see method codes)
    • 1: Near Infrared Spectroscopy
    • 2: ICP Analysis
    • 3: TKN digestion
    • 4: Microwave digestion
    • 5: TKN Analysis
    • 6: CHN Analysis
    • 7: DCP Analysis
    • 8: Dry Ash
16. nitrogen: percent nitrogen (unit: dimensionless / missing value: NA)
17. nitrogen.method: code for method used to digest and/or analyze samples (see method codes)
    • 1: Near Infrared Spectroscopy
    • 2: ICP Analysis
    • 3: TKN digestion
    • 4: Microwave digestion
    • 5: TKN Analysis
    • 6: CHN Analysis
    • 7: DCP Analysis
    • 8: Dry Ash