LAKE FRYXELL CILIATES, BACTERIA, NANOFLAGELLATES


Acceptance and utilization of LTER data requires that:


LAKE FRYXELL CILIATES, BACTERIA, NANOFLAGELLATES

FILE NAME: ciliates.datData File (Comma Delimited Ascii Format)
ciliates.txtData File (MS-DOS Text - Table Layout).

PRINCIPAL INVESTIGATOR: Johanna Laybourn-Parry
Address:Institute of Environmental Sciences
University of Nottingham - Sutton Bonington Campus
Loughborough, LE12 5RD, United Kingdom
Phone:+44 115 951 6262
E-Mail:J.Laybourn-Parry@nottingham.ac.uk

OTHERS: Diane McKnight
INSTAAR
1560 30th Street
Campus Box 450
Boulder, CO 80309-0450
(303) 492-4687
AND
John Priscu
Department of Biology
309 Lewis Hall
Montana State University
Bozeman, MT 59717
(406) 994-3250

KEYWORDS: lake, flagellate, nanoflagellate, heterotrophic, phototrophic, bacteria, ciliate, Antarctica, limnology, microzooplankton

ABSTRACT: In conjunction with the Long Term Ecological Research (LTER) project in the McMurdo Dry Valleys of Antarctica, lakes were monitored for microzooplankton by a team based out of the University of Nottingham (led by Johanna Laybourn-Parry). This dataset shows numbers of ciliates, bacteria, heterotrophic nanoflagellates, and phototrophic nanoflagellates found at various depths in Lake Fryxell.

VARIABLES: location, date, depth, #ciliates, #Askenasia, #S_Monodinium, #L_Monodinium, #Strombidium, #Vorticella, #Bursaria, #Sphaerophyra, #bacteria, #HNAN, #PNAN

RESEARCH LOCATION: Lake Fryxell (77°37' S, 163°07' E) has an area of 7 km2 and a maximum depth of 19 m. The average depth is 9 m and therefore the lake has an extensive littoral zone (above a depth of 9 m) where microbial mats are abundant. The lake is chemically stratified with an oxic zone extending down to 9.5 m. A distinct oxycline is present between 7.5 and 9.5 m below which the waters are anoxic. The lake is permanently stratified. The upper waters are low in nutrients (NH4+, NO2-, NO3-, and PO4-) but ammonium and soluble reactive phosphorus increase below the oxycline. Thus the upper waters experience a combination of low temperatures, nutrient limitation and highly attenuated light because of ice cover.

METHODS: Water was collected using either a Kemmerer bottle or a Van Dorn sampler lowered through a hole in the 4-m-thick ice with a Jiffy-drill in January 1992 and in January 1994 at a center station (depth 18.5 m). Samples were taken at 1-m intervals down to 12 m into the anoxic zone. In 1992, 250-ml subsamples were fixed in Lugol's iodine for the analysis of ciliates, and other aliquots fixed in glutaraldehyde for bacterial counts. In 1994, 1.1-l samples were fixed in buffered glutaraldehyde for protozoological and bacterial analysis. These were kept refrigerated in the dark and flown to Australia or New Zealand for immediate analysis. Both fixatives are regarded as reliable for protistan analysis provided samples are analysed within a few months of collection. However, in our experience while Lugol's iodine is considered best for preserving abundance, it does cause more cell distortion of some species than glutaraldehyde, which gives better preservation of ciliates in freshwater samples. One liter of water from each depth was preserved in Lugol's iodine for phytoplankton counts. Temperature was measured with a (YSI) Yellow Springs Instruments 54 meter and probe, and conductivity with a Radiometer Conductivity meter.

Ten milliliters of the buffered glutaraldehyde-fixed material was stained with DAPI, and filtered onto a 0.2-µm black polycarbonate filter, and bacterial numbers were counted under epifluorescence microscopy using UV excitation. Fifty milliliters was stained with DAPI, filtered onto 1.0-µm polycarbonate filters and viewed under epifluorescence microscopy using both blue and UV filters to determine heterotrophic and autotrophic flagellate abundances. The larger protozooplankton in each 1-l sample of glutaraldehyde-fixed water were concentrated by settling, stained with bromophenol blue and counted in Sedgewick-Rafter counting chambers under DIC microscopy at x320. Detailed analysis was undertaken under higher magnification using both DIC and phase microscopy. For phytoplankton analysis between 5 and 50 ml was subsampled. These phytoplankton were settled and enumerated using the inverted microscope method of Utermohl.

TIMING: Samples were gathered in January 1992 and January 1994.

CITATIONS: Laybourn-Parry, Johanna, Mark R. James, Diane M. McKnight, John Priscu, Sarah A. Spaulding, and Russell Shiel. 1997. The microbial plankton of Lake Fryxell, southern Victoria Land, Antarctica during the summers of 1992 and 1994. Polar Biology. 17: 54-61.

COMMENTS:

STATUS: Restricted Access (Type IV).

VARIABLE DESCRIPTION:

VARIABLE

TYPE

DESCRIPTION

UNITS

MISSING VALUE INDICATOR

MINIMUM

MAXIMUM

PRECISION

Location

Text

Name of lake where measurement was made

none

Required entry

n/a

n/a

n/a

Date

Date

Date on which sample was gathered

mmm-yyyy

Required entry

Jan-1992

Jan-1999

mm

Depth (m)

Number

Depth at which sample was drawn from lake

meters

Required entry

1

12

1

#Ciliates

Number

Number of ciliates counted/liter of lake water

# / liter

Required entry

n/a

n/a

n/a

#Askenasia

Number

Number of Askenasia organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#S_Monodinium

Number

Number of S_Monodinium organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#L_Monodinium

Number

Number of L_Monodinium organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#Strombidium

Number

Number of Strombidium organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#Vorticella

Number

Number of Vorticella organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#Bursaria

Number

Number of Bursaria organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#Sphaerophyra

Number

Number of Sphaerophyra organisms counted/liter of lake water

# / liter

Required entry

0

n/a

1

#Bacteria

Number

Number of bacteria x 108 counted/liter of lake water

# x 108/ liter

Required entry

0

n/a

1

#HNAN

Number

Number of heterotrophic nanoflagellates x 105 counted/liter of lake water

# x 105/ liter

Required entry

0

n/a

1

#PNAN

Number

Number of phototrophic nanoflagellates x 105 counted/liter of lake water

# x 105/ liter

Required entry

0

n/a

1

LOG: Data for this file was submitted by Johanna Laybourn-Parry to the data manager at INSTAAR on October 21, 1998. Files were sent via e-mail as well as a hard copy. The original version of the file is stored on the Unix system in "/data1/data/lakes/plankton/laybourn-parry/Fryxell". Upon arrival at INSTAAR, the data manager reformatted the file to present it in a relational mode. This was done using Microsoft Access. It was then exported in comma delimited ascii and MS-DOS text format to present on the web. Links to these files are provided above.

NOTE: Data contained in these files has been subjected to quality control standards imposed by the investigator. The user of this data should be aware that, while efforts have been taken to ensure that these data are of the highest quality, there is no guarantee of perfection for the data contained herein and the possibility of errors exists. If you encounter questionable data, please contact the MCM LTER data manager (; (303)492-4639) so that the data can be corrected or qualified. Thus, these data may be modified and future data will be appended.