Demographic genetics of the American beech, Fagus grandifolia. II. Genet substructure of populations for the Blue Ridge, Piedmont and the Great Smoky Mountains

Populations of American beech in Virginia and the Great Smoky Mountain National Park in Tennessee and North Carolina were investigated for demographic genetic substructurings. Two Virginia populations, one on the Blue Ridge (WG1) and the other on the Piedmont (WG2) occur over an elevational gradient of several hundreds meters. One of the Great Smoky Mountain populations (GS1) was in a 'beech gap' and the other (GS2) in a 'cove forest' along a creek. The populations in the Great Smoky Mountain National Park were only separated by a few hundred meters in elevation, but both on the same physiographic province. The populations had two growth forms. Trees produced extensive root suckers at WG1, GS1 and GS2, but WG2 had no root suckers and all individuals had obviously been established from seeds. A total of 1335 shoots were mapped at the four sites, their size measured [diameter at breast height (DBH) or diameter at ground height (DGH)], and genotypes were determined for each locus using allozyme analysis. F_IS among five different size-classes revealed an excess of homozygotes in WG1, GS1 and GS2, and an excess of heterozygotes in WG2. The offshoot formation from root suckers obviously contributed to the abundance of intermediate size-classes in WG1, GS1 and GS2. Exceedingly localized patchiness of different multilocus genotypes reveals genetic clustering of shoots that have obviously originated from root suckers in WG1, GS1 and GS2. The Piedmont population (WG2), on the other hand, showed loose localization of genetically related trees at a scale of 35–40 m in area, suggesting broader ranges of pollen and seed dispersal. The data are discussed in the light of the differences in growth form and mode of reproduction, and also in relation to the post-glacial migration and the current geographic distribution of the species.     

Seed bank spatial pattern in a temperate secondary forest

Abstract. Seed bank spatial pattern was studied in a secondary forest dominated by Fagus sylvatica and Betula celtiberica in the Urkiola Natural Park (N Spain). Soil samples were taken every 2 m in a regular grid (196 points) and divided into two fractions (0–3 cm and 3–10 cm deep). The viable seed bank was studied by monitoring seedling emergence for ten months. The effect of different factors on seed bank composition and patterning was analysed using constrained ordination as a hypothesis testing tool. Furthermore, the existence of spatial autocorrelation was evaluated by geostatistical analysis. Seed density was high, 7057 seed.m^?2, with a few species dominating. Species composition in the various layers were significantly correlated. The seed bank showed significant spatial structure, which was partially explainable by the spatial structure of the canopy and understorey vegetation. Spatial clumping from 0–8 m was observed in seed bank density and composition, mainly due to the pattern of two abundant taxa Juncus effusus and Ericaceae. The Ericaceae seed bank was related to the spatial distribution of dead stumps of Erica arborea. J. effusus was not present in the above‐ground vegetation, which indicates that its seed bank was formed in the past. As expected, the seed bank of this forest reflects its history, which is characterized by complex man‐induced perturbations. The seed bank appears to be structured as a consequence of contrasting driving forces such as canopy structure, understorey composition and structural and microhabitat features.     

Stomata of trees growing in CO2-enriched air show reduced sensitivity to vapour pressure deficit and drought

Stomatal conductance ( g _s) and photosynthetic rate ( A ) were measured in young beech ( Fagus sylvatica ), chestnut ( Castanea sativa ) and oak ( Quercus robur ) growing in ambient or CO₂-enriched air. In oak, g _s was consistently reduced in elevated CO₂. However, in beech and chestnut, the stomata of trees growing in elevated CO₂ failed to close normally in response to increased leaf-to-air vapour pressure deficit (LAVPD). Consequently, while g _s was reduced in elevated CO₂ on days with low LAVPD, on warm sunny days (with correspondingly high LAVPD) g _s was unchanged or even slightly higher in elevated CO₂. Furthermore, during drought, g _s of beech and chestnut was unresponsive to [CO₂], over a wide range of ambient LAVPD, whereas in oak g _s was reduced by an average of 50% in elevated CO₂. Stimulation of A by elevated CO₂ in beech and chestnut was restricted to days with high irradiance, and was greatest in beech during drought. Hence, most of the additional carbon gain in elevated CO₂ was made at the expense of water economy, at precisely those times (drought, high evaporative demand) when water conservation was most important. Such effects could have serious consequences for drought tolerance, growth and, ultimately, survival as atmospheric [CO₂] increases.     

Semiochemical attractants for the beech leaf‐mining weevil,Orchestes fagi

The beech leaf‐mining weevil, Orchestes fagi L. (Curculionidae: Curculioninae: Rhamphini), a pest of European beech, Fagus sylvatica L. (Fagaceae), was recently discovered infesting American beech, Fagus grandifolia Ehrh., in Nova Scotia, Canada. Adult O. fagi feed on both young and mature leaves of beech as well as on other species (e.g., raspberry, Rubus spp.), but oviposition and larval feeding are restricted to beech. Females oviposit in young developing beech leaves at the time of bud burst. We characterized volatiles emitted from buds, leaves, and sapwood of American beech and examined their potential as attractants alone or when combined with other weevil pheromones for O. fagi. We predicted that adults would be attracted to volatiles emitted from beech leaves, especially those emitted from bursting beech buds. Gas chromatography/mass spectrometry (GC/MS) analyses of volatiles collected from buds at pre‐ and post‐budburst identified two diterpene hydrocarbons, 9‐geranyl‐p‐cymene ( 1 ) and 9‐geranyl‐α‐terpinene ( 2a ), that were emitted in large amounts at the time of bud burst. Compound 1 significantly increased mean catch of males and total O. fagi (but not females) on sticky traps compared with unbaited controls. Y‐tube bioassays confirmed attraction of male O. fagi to bursting beech buds and compound 1 . Attraction of male O. fagi to 1 , emitted in large quantities from American beech, is likely adaptive because both oviposition and mating of O. fagi coincide with budburst. Our data suggest that traps baited with 1 may be useful for monitoring the spread of O. fagi in North America.     

Forest History as a Basis for Ecosystem Restoration—A Multidisciplinary Case Study in a South Swedish Temperate Landscape

Basic knowledge of the previous forest types or ecosystem present in an area ought to be an essential part of all landscape restoration. Here, we present a detailed study of forest and land use history over the past 2,000 years, from a large estate in southernmost Sweden, which is currently undergoing a restoration program. In particular, the aim was to identify areas with long continuity of important tree species and open woodland conditions. We employed a multidisciplinary approach using paleoecological analyses (regional and local pollen, plant macrofossil, tree ring) and historical sources (taxation documents, land surveys, forest inventories). The estate has been dominated by temperate broad‐leaved trees over most of the studied period. When a forest type of Tilia, Corylus, and Quercus started to decline circa 1,000 years ago, it was largely replaced by Fagus. Even though extensive planting of Picea started in mid‐nineteenth century, Fagus and Quercus have remained rather common on the estate up to present time. Both species show continuity on different parts of the estate from eighteenth century up to present time, but in some stands, for the entire 2,000 years. Our suggestions for restoration do not aim for previous “natural” conditions but to maintain the spatial vegetational pattern created by the historical land use. This study gives an example of the spatial and temporal variation of the vegetation that has historically occurred within one area and emphasizes that information from one methodological technique provides only limited information about an area’s vegetation history.     

Gas exchange and antioxidative compounds in young beech trees under free-air ozone exposure and comparisons to adult trees

Three-year-old beech (Fagus sylvatica) seedlings growing in containers were placed into the sun and shade crown of a mature beech stand exposed to ambient (1 x O(3)) and double ambient (2 x O(3)) ozone concentrations at a free-air exposure system ("Kranzberg Forst", Germany). Pigments, alpha-tocopherol, glutathione, ascorbate, and gas exchange were measured in leaves during 2003 (a drought year) and 2004 (an average year). Sun-exposed seedlings showed higher contents of antioxidants, xanthophylls, and beta-carotene and lower contents of chlorophyll, alpha-carotene, and neoxanthin than shade-exposed seedlings. In 2003 sun-exposed seedlings showed higher contents of carotenoids and total glutathione and lower net photosynthesis rates (A(max)) compared to 2004. O(3) exposure generally affected the content of chlorophyll, the xanthophyll cycle, and the intercellular CO(2) concentration (c(i)). Seedlings differed from the adjacent adult trees in most biochemical and physiological parameters investigated: Sun exposed seedlings showed higher contents of alpha-tocopherol and xanthophylls and lower contents of ascorbate, chlorophyll, neoxanthin, and alpha-carotene compared to adult trees. Shade exposed seedlings had lower contents of xanthophylls, alpha-carotene, and alpha-tocopherol than shade leaves of old-growth trees. In 2003, seedlings had higher A(max), stomatal conductance (g(s)), and c(i) under 2 x O(3) than adult trees. The results showed that shade acclimated beech seedlings are more sensitive to O(3), possibly due to a lower antioxidative capacity per O(3) uptake. We conclude that beech seedlings are uncertain surrogates for adult beech trees.