33 Works

Lake Peipsi 2009 (Phytoplankton samples)

Kristel Panksep, Olga Buhvestova, Ave Pent, Kätlin Blank, Kai Ginter & Reet Laugaste
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 2005 (Phytoplankton samples)

Reet Laugaste, Külli Kangur & Kadi Palmik
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1993 (Phytoplankton samples)

Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 1992 (Phytoplankton samples)

Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 2014 (Phytoplankton samples)

Reet Laugaste, Külli Kangur, Kadi Palmik, Ave Pent, Marina Haldna & Olga Tammeorg
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1987 (Phytoplankton samples)

Lokk Saida & Reet Laugaste
Method: Up to 1988 the samples were preserved with formaldehyde (not neutralised), and lots of samples were spoiled: sample sediment was flaked, stuck together, or rusty. By this reason, a number of results of countings are not representative.

Lake Peipsi 2010 (Phytoplankton samples)

Olga Buhvestova, Külli Kangur, Kadi Palmik, Kristel Panksep, Ave Pent & Reet Laugaste
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 2007 (Phytoplankton samples)

Reet Laugaste, Kätlin Krikmann, Olga Buhvestova & Külli Kangur
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1994 (Phytoplankton samples)

Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 1988 (Phytoplankton samples)

Reet Laugaste
Method: Up to 1988 the samples were preserved with formaldehyde (not neutralised), and lots of samples were spoiled: sample sediment was flaked, stuck together, or rusty. By this reason, a number of results of countings are not representative.

Lake Peipsi 1985 (Phytoplankton samples)

Reet Laugaste
Method: Up to 1988 the samples were preserved with formaldehyde (not neutralised), and lots of samples were spoiled: sample sediment was flaked, stuck together, or rusty. By this reason, a number of results of countings are not representative.

Lake Peipsi 2003 (Phytoplankton samples)

Reet Laugaste
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1999 (Phytoplankton samples)

Reet Laugaste
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 2000 (Phytoplankton samples)

Reet Laugaste & Külli Kangur
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1997 (Phytoplankton samples)

Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 2006 (Phytoplankton samples)

Reet Laugaste, Külli Kangur & Aimar Rakko
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 2004 (Phytoplankton samples)

Reet Laugaste & Külli Kangur
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1995 (Phytoplankton samples)

Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 1996 (Phytoplankton samples)

Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 2001 (Phytoplankton samples)

Reet Laugaste
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1989 (Phytoplankton samples)

Saida Lokk & Reet Laugaste
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Lake Peipsi 1984 (Phytoplankton samples)

Reet Laugaste
Method: Up to 1988 the samples were preserved with formaldehyde (not neutralised), and lots of samples were spoiled: sample sediment was flaked, stuck together, or rusty. By this reason, a number of results of countings are not representative.

Lake Peipsi 2008 (Phytoplankton samples)

Reet Laugaste, Kristel Panksep, Olga Buhvestova, Külli Kangur, Kadi Palmik, Ave Pent, Kätlin Blank & Kai Ginter
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 2011 (Phytoplankton samples)

Olga Buhvestova, Külli Kangur, Kristel Panksep & Reet Laugaste
Method: Phytoplankton samples were preserved in Lugol’s (acidified iodine) solution and counted under an inverted microscope (Utermöhl, 1958). 3 ml of preserved sample was settled overnight and counted in random fields or transects. Biovolumes of algal cells, colonies and/or filaments were calculated using assigned geometric shapes dimensions, and converted to biomass assuming the specific density of 1 g cm-3 in accordance with Edler (1979). Approved by CEN on 14 July 2006 “Water quality - Guidance...

Lake Peipsi 1998 (Phytoplankton samples)

Reet Laugaste & Aimar Rakko
Methods: Samples were in most cases concentrated by precipitation up to 15 ml. Count was made on striped microscope slides within volume 0,1 ml. Microscopes: MBI-3 (magnification 15x20 and 15x40) and Jenaval (7x40). Macroscopic colonies of Gloeotrichia echinulata were counted visually in 500 ml measuring cylinder.

Registration Year

  • 2019
    33

Resource Types

  • Dataset
    33