Abstract:
Data for Crooked Lake and Lake Druzhby (CL and LD), Vestfold Hills.Programme Dec 98 - Feb 00
PI: Prof J Laybourn-Parry
Winterer: Tracey Henshaw (any questions regarding the data sheets:
plxtlh@nottingham.ac.uk)
Four sites were sampled in the two lakes
Cl - 68 36 30 S 78 21 50 E
LD1 - 68 35 47 S 78 14 56 E
LD2 - 68 35 15 S 78 18 00 E
LD3 - 68 35 40 S 78 19 20 E
Originally the sites were known by
... names;
LD1 - Watts site
LD2 - LDD or LD deep site
LD3 - LDS or LD Shallow or LD Upper site
Folders
There are four folders (Physical, Chemical, Biological and Production Data) each containing the relevant workbooks ie: ammonia, heterotrophic bacteria etc Within each workbook, each sites' data set is on a seperate sheet (with any related graphs) with any special notes regarding that data set.
Notes
Chemical Folder - all units are micrograms per litre
Physical folder - all units specified on the sheets.
Biological Folder - Chl a is in micrograms per litre.
Some microscopy samples were counted by Johanna Laybourn-Parry and so there are no data available for sizing or for heterotropic bacteria rods v cocci. These are mainly in Nov 99 and indicated on the sheet as 'JLP' and nd. CL does not contain cyanobacteria, so there are no entries for CL in the cyano workbook.
PNAN and HNAN, ciliates and rotifers were sized once in Nov 99 to give a carbon pool snapshot. PNAN and HNAN sizing data are in the PNAN and HNAN workbook, ciliate and rotifer abndance and sizing is in the carbon pool workbook.
Total biomass data are also in the carbon pool workbook.
Production Folder - Bacterial production (ng C l-1h-1) raw data are given, calculations are to the left of the raw data and graphs at the bottom of the data.
Fractionation and Nutrient addition workbooks relate to work done seperating the bacterial fraction into free and aggregate associated bacterial fractions and to spiking with nutrients and measuring production.
Graphs
Many of the graphs do not have labelled X axes (as decimal dating was used throughout) but dates are given with the data.
Sampling
Sites LD1 and LD3 were shallow sites, so samples were originally taken from 3 depths but this was reduced in June/July to two depths. Sites CL and LD2 are deep sites and samples were originally taken from 0, 2, 4, 6, 8, 10, 15, 20, 30, 40 m but this was reduced in Mar/May to 0, 2, 5, 8, 10, 15, 20 and 40m.
Several sampling sites for LD1 and LD3 were tried at the start of the programme (denoted as 'old' or 1x 1a sites on the spreadsheets).
In January 00 only one sample from LD1 and LD3 was collected.
Sampling Dates
Sampling dates vary between the sites, but are given with each data set. There may appear to be discrepancies for example, LDS ammonia sampled on 21 Jan but DOC on 25 Jan - but sampling was broken down at the start while I learnt the technique
The fields in this dataset are:
Ammonia concentration
Heterotrophic bacteria
Cyanobacteria abundance
Ciliates
Rotifers
nitrite
nitrate
temperature
oxygen (O)
cysts
biomass
volume
PH
conductivity
light data
phosphorus concentrations
saturation
conditions
air temperature
ice thicknes
factionation
chlorophyll a isoclines
standard deviation
mean
conversion factor
carbon produced 
