|
Biodiversity
Landscape Development
Management of Natural Hazards
Natural Resources
Forest Ecosystems
Research Units
In focus
Staff
Organization
Mission and Tasks
Locations
History
Job opportunities
Contact and maps
Searching for the origin of the so-called Bödmerenwald-spruce
BackgroundThe so-called Bödmerenwald-spruce is a geographically limited population of Picea abies forming one of the few near-natural spruce forests in the Alps (46° 59’ N, 8° 51’ E), part of which is now under protection. Earlier we showed that this forest is part of a geographically larger but clearly defined population with a unique genetic signature and high genetic diversity of mitochondrial DNA bounded within Switzerland on the east, south, and west by spruce of extremely low diversity, whereas the northern limits are still unclear due to introduction of spruce of foreign origin but might lie in southern Germany (Sperisen et al. 2005). Geographically, the high genetic diversity of these forests interrupts the general genetic pattern in the Alps, grading from high genetic diversity in the eastern Alps to low in the western Alps (including most of Switzerland), a pattern that is understood to result from successive founder events during the general east-to-west expansion of spruce in the Holocene (Gugerli et al. 2001). Van der Knaap et al. (2005) and Latalowa & van der Knaap (2006) traced this spruce expansion by means of pollen data. The timing of the Bödmerenwald-spruce expansion around 7000 years ago is in line with the general east-to-west spruce migration through the Alps, but speed of expansion falls out of the pattern. Westward expansion was rapid from the far eastern Alps to the Jura Mountains in the west, except for a narrow north-south oriented strip just over the Bödmerenwald area where it was extremely slow: less than 50 km expansion in two millennia (8000-6000 yr BP). So both the genetic structure and the early expansion history stand out from the general patterns, and it is tempting to think that the two are related. Objectives
MethodsWork with aDNA will be carried out in two independent laboratories (Birmensdorf and Copenhagen) to validate results. Extraction of aDNA and PCR setup will be performed in clean laboratory facilities, physically separated from other laboratories and equipped with air over-pressure and laminar flows with UV-radiation. Extraction of aDNA will follow the protocols established in Birmensdorf (Liepelt et al. 2006) and Copenhagen. Variation will be assessed in the second intron of the mitochondrial nad1 gene (Sperisen et al. 2001). Partners
References
|