No abstract

A better understanding of germination and seedling establishment is needed for conservation of orchid populations. Due to the obligate association with a mycobiont, the germination niches in orchid species are extremely complex and varied. Microsites suitable for germination can be small and transient, and direct observation is difficult. An experimental approach using several levels of environmental manipulation/control is recommended.

Orchid mycorrhiza probably affects about 25 000 plant species and thus roughly one tenth of all higher plants.Histologically, this symbiosis resembles other kinds of endomycorrhiza, the fungal hyphae growing within living plant cells. Considerable evidence, however, suggests that it is not a two-way exchange relationship and thus not potentially mutualistic, such as the wide-spread endomycorrhiza between plants and Glomalean fungi, known as arbuscular mycorrhiza. During the achlorophyllous seedling stage orchids are obligately dependent on the fungi; some species remain so through life, while others establish photosynthesis but to varying degrees remain facultatively dependent of / responsive to fungal infection as adults. None of the fungi involved are so far known to depend on the symbiosis with orchids. Transfer of organic carbon compounds from hyphae to the orchid has been demonstrated repeatedly, but it is not clear to what extent this takes place during a biotrophic phase while the intracellular hyphae remain intact, or during the subsequent extensive degradation of the hyphal coils. The advantage of viewing orchid mycorrhiza basically as a unilateral mycophagous relationship, in spite of hypothetical beneficial spin-offs to the mycobiont, is that it provides a conceptual framework similar to that of other parasitic or fungivore relationships; mechanisms known in such relationships could be searched for in future studies of the orchidÁfungus symbiosis. These could include mechanisms for recognition, attraction and selection of fungi, physiological regulation of internal hyphal growth, breakdown, and material transfer, nutritional consequences of the plant's preference(s) and trophic changes, fungal avoidance mechanisms, and consequences at population and ecosystem levels. A whole range of possible life strategies becomes apparent that could support divergent evolution and lead to the proliferation of species that has indeed occurred in the orchid family. We outline some of the possible physiological mechanisms and ecological implications of this approach.

A method is described by which seeds of terrestrial orchids are sown and retrieved in the field under almost natural conditions. For the first time it is possible to conduct a quantitative study of orchid germination in situ and observe seasonal growth and mortality of seedlings. The technique has also enabled us to investigate the relation between the site where the seeds are sown, the availability of an appropriate fungus to infect the seeds, and seedling establishment in the soil. Five local species were studied. Corallorhiza odontorhiza, Goodyera pubescens, and Galearis spectabilis all began to germinate in May–June, after 23‐30 weeks in the soil. These species differed in their dependency on infection at germination time, but none of the seedlings developed beyond the point of rupturing the testa except when infected. Seeds of Liparis lilifolia and Tipularia discolor did not germinate within the first 12 months of the experiment. The implications and potential uses of this field sowing technique for further studies and for other kinds of minute seeds are discussed.

Building performance can be expressed by different indicators as primary energy use, environmental load and/or the indoor environmental quality and a building performance simulation can provide the decision maker with a quantitative measure of the extent to which an integrated design solution satisfies the design requirements and objectives. In the design of sustainable Buildings it is beneficial to identify the most important design parameters in order to develop more efficiently alternative design solutions or reach optimized design solutions. A sensitivity analysis makes it possible to identify the most important parameters in relation to building performance and to focus design and optimization of sustainable buildings on these fewer, but most important parameters. The sensitivity analyses will typically be performed at a reasonably early stage of the building design process, where it is still possible to influence the important parameters. The methodology is presented and an application example is given for design of an office building in Denmark.

No abstract

The abundance and reproductive activity of orchids have been linked to variations in weather conditions, but few investigators have examined the relationships between orchid flowering dynamics and the distribution and abundance of mycorrhizal fungi. We quantified the abundance of flowering individuals of Corallorhiza odontorhiza, a mycoheterotrophic orchid, over a 14-year period and mapped the distribution of individuals in six of the 14 years. For two seasons, we conducted intensive and extensive studies of the mycorrhizal fungi that were associated with C. odontorhiza. The annual abundance of flowering plants was statistically related to growing-season precipitation and winter temperature, and the distribution of individuals within the study plot was related to the abundance and distribution of appropriate host fungi. We used DNA sequencing to identify ectomycorrhizal root tips that hosted Tomentella fungi that could potentially support C. odontorhiza. We found that Tomentella spp. were distributed throughout the study plot and on all ectomycorrhizal tree species, including in areas that have historically supported few or no orchids. However, there were fewer ectomycorrhizal trees, total ectomycorrhizal root tips, and root tips hosting Tomentella spp. in areas with few or no orchids compared to areas with abundant orchids. Furthermore, one Tomentella taxon dominated in C. odontorhiza rhizomes but was never found except immediately adjacent to C. odontorhiza plants. This suggests that abundance of flowering C. odontorhiza reflects both the presence of ''preferred'' taxa and abundance of appropriate host fungi associated with ectomycorrhizal roots. Results of this research provide the first indication that the relationship between plants and mycorrhizal fungi may be influenced by both the relative abundance of fungi that are sufficient to support orchid growth and by the presence of particular fungal types that are especially good at supporting orchid growth.

clinicaltrials.gov Identifier: NCT00207064.