Spatial Interrelationships of Deciduous Forest Herbs

1990 ◽  
Vol 117 (2) ◽  
pp. 101 ◽  
Author(s):  
Robert N. Muller
Keyword(s):  
Deciduous Forest ◽  
Forest Herbs

scholarly journals Frequency-Dependent Seed Dispersal by Ants of Two Deciduous Forest Herbs

Ecology ◽  
1989 ◽  
Vol 70 (6) ◽  
pp. 1645-1648 ◽  
Author(s):  
Brent H. Smith ◽  
Catherine E. deRivera ◽  
Cara Lin Bridgman ◽  
John J. Woida
Keyword(s):  
Seed Dispersal ◽  
Deciduous Forest ◽  
Frequency Dependent ◽  
Forest Herbs

Habitat may limit herb migration at the northern edge of the Appalachian deciduous forest *This paper is dedicated to our botanical mentor, the late Dr. Sam P. Vander Kloet.

Botany ◽  
2011 ◽  
Vol 89 (9) ◽  
pp. 635-645 ◽  
Author(s):  
Nicholas M. Hill ◽  
David J. Garbary
Keyword(s):  
Species Richness ◽  
Sugar Maple ◽  
Deciduous Forest ◽  
Soil Calcium ◽  
Forest Herbs ◽  
Migration Corridors ◽  
Habitat Factors ◽  
History Of ◽  
Calcium Magnesium ◽  
Northern Edge

Forest herbs account for greater species richness than any other plant type in deciduous forests and are the most vulnerable to anthropogenic disturbances. We examined whether the limited distribution of rare Appalachian forest herbs in Nova Scotia is related to edaphic specialization or a history of anthropogenic disturbance. Remnant populations are restricted to floodplain forest, where both habitat factors and disturbance history differ significantly from those of adjacent upland sugar maple forest. Contrasting soil and litter layers between floodplain stands and adjacent upland sites revealed the latter to be deficient in key cations (calcium, magnesium, boron); however, regression models for uplands and for floodplains showed that native herb richness was related to soil fertility in each case. Soil calcium accounted for most of the species richness variation among floodplains for native herbs and for a large seeded guild that contains most of the rare species on floodplains. Given the widespread anthropogenic decalcification of forest soils throughout eastern North America, conservation efforts must (i) increase and connect deciduous forest floodplain ecosystems and (ii) understand how to manage and create suitable cation-rich migration corridors in the forest landscape.

The morphology of vesicular – arbuscular mycorrhizae in Clintonia borealis and Medeola virginiana

1996 ◽  
Vol 74 (5) ◽  
pp. 679-685 ◽  
Author(s):  
Paul Widden
Keyword(s):  
Arbuscular Mycorrhizae ◽  
Deciduous Forest ◽  
Arbuscular Mycorrhizal ◽  
Cortical Layer ◽  
Cortical Cells ◽  
Vesicular Arbuscular Mycorrhizae ◽  
Forest Herbs ◽  
Vesicular Arbuscular ◽  
Innermost Layer ◽  
Inner Cortex

During a survey of the vesicular–arbuscular mycorrhizal (VAM) associations of forest herbs in a deciduous forest in the southern Laurentian mountains in Quebec, two liliaceous species, Clintonia borealis and Medeola virginiana, revealed very distinctive morphology. In both species, once the epidermis was penetrated, the fungus spread towards the centre of the root via intracellular hyphae until the innermost layer of the cortex was reached, at which point the fungus spread laterally and tangentially through the cortical cells adjacent to the endodermis via a series of banana-shaped projections (bobbits). These eventually differentiated into the arbuscules and the VAM might spread from this inner cortical layer back into the outer cortical layers. In C. borealis, the hyphae coiled in the cortex, and vesicles were formed in the upper cortical cells. In M. virginiana, no coiling took place, but extensive diverticulae were produced by the intracellular hyphae in the cortical cells, close to their point of exit, and vesicles were produced in the inner cortex as swellings from the bobbits. These two mycorrhizae have some similarities to one in Colchicum autumnale described by I. Gallaud (1905. Rev. Gen. Bot. 17). Keywords: vesicular–arbuscular mycorrhizae, Clintonia borealis, Medeola virginiana, Liliaceae, morphology.

Effects of simulated post-harvest light availability and soil compaction on deciduous forest herbs

2002 ◽  
Vol 32 (10) ◽  
pp. 1753-1762 ◽  
Author(s):  
Christine J Small ◽  
Brian C McCarthy
Keyword(s):  
Soil Compaction ◽  
Deciduous Forest ◽  
Light Availability ◽  
Natural Disturbance ◽  
Deciduous Forests ◽  
Herbaceous Plant ◽  
Eastern Deciduous Forest ◽  
Forest Herbs ◽  
Successional Species ◽  
Eastern Deciduous Forests

To better understand the response of eastern deciduous forest herbs to microenvironmental changes associated with logging, the effects of experimental light and soil compaction treatments were examined in six herbaceous plant species characteristic of varying successional stages. We found severe growth reductions and increased mortality of Osmorhiza claytonii (Michx.) C.B. Clarke, a shade-tolerant forest perennial, when grown in full sun and greater soil compaction. Deeply shaded conditions, similar to those beneath regenerating forests, resulted in reduced growth of early successional species such as Galium aparine L., and Eupatorium rugosum Houtt. Growth of other species such as Geum canadense Jacq., and Elymus hystrix L. appeared to increase in the patchy, intermediate light treatment mimicking mature eastern deciduous forests. Soil compaction caused severe reductions in height and biomass of Eupatorium rugosum and O. claytonii, early- and late-successional species, respectively. While harvested stands experience relatively uniform light environments, canopy gaps and sunflecks in mature eastern deciduous forests create heterogeneous light environments often correlated with recruitment, growth, and diversity of understory herbs. Therefore, management approaches that minimize alteration of forest environments and mimic natural disturbance patterns may be important to the maintenance and regeneration of forest herbs.

Differentiation of new coenomorph in context of the Belgard’s ecomorph system development

2017 ◽  
Vol 28 (1-2) ◽  
pp. 28-35 ◽  
Author(s):  
B. A. Baranovski
Keyword(s):  
Environmental Factors ◽  
Plant Species ◽  
Vascular Plants ◽  
Deciduous Forest ◽  
System Development ◽  
Vascular Plant ◽  
Tabular Form ◽  
Ecological Scales ◽  
The One ◽  
Different Levels

Nowadays, bioecological characteristics of species are the basis for flora and vegetation studying on the different levels. Bioecological characteristics of species is required in process of flora studying on the different levels such as biotopes or phytocenoses, floras of particular areas (floras of ecologically homogeneous habitats), and floras of certain territories. Ramensky scale is the one of first detailed ecological scales on plant species ordination in relation to various environmental factors; it developed in 1938 (Ramensky, 1971). A little later (1941), Pogrebnyak’s scale of forest stands was proposed. Ellenberg’s system developed in 1950 (Ellenberg, 1979) and Tsyganov’s system (Tsyganov, 1975) are best known as the systems of ecological scales on vascular plant species; these systems represent of habitat detection by ecotopic ecomorphs of plant species (phytoindication). Basically, the system proposed by Alexander Lyutsianovich Belgard was the one of first system of plant species that identiified ectomorphs in relation to environmental factors. As early as 1950, Belgard developed the tabulated system of ecomorphs using the Latin ecomorphs abbreviation; he also used the terminology proposed in the late 19th century by Dekandol (1956) and Warming (1903), as well as terminology of other authors. The article analyzes the features of Belgard’s system of ecomorphs on vascular plants. It has certain significance and advantages over other systems of ecomorphs. The use of abbreviated Latin names of ecomorphs in tabular form enables the use shortened form of ones. In the working scheme of Belgard’s system of ecomorphs relation of species to environmental factors are represented in the abbreviated Latin alphabetic version (Belgard, 1950). Combined into table, the ecomorphic analysis of plant species within association (ecological certification of species), biotope or area site (water area) gives an explicit pattern on ecological structure of flora within surveyed community, biotope or landscape, and on environmental conditions. Development and application by Belgrard the cenomorphs as «species’ adaptation to phytocenosis as a whole» were completely new in the development of systems of ecomorphs and, in this connection, different coenomorphs were distinguished. Like any concept, the system of ecomorphs by Belgard has the possibility and necessity to be developed and added. Long-time researches and analysis of literature sources allow to propose a new coenomorph in the context of Belgard’s system of ecomorphs development: silvomargoant (species of forest margin, from the Latin words margo – edge, boundary (Dvoretsky, 1976), margo – margin, ad margins silvarum – along the deciduous forest margins). As an example of ecomorphic characterization of species according to the system of ecomorphs by Belgard (when the abbreviated Latin ecomorph names are used in tabular form and the proposed cenomorph is used), it was given the part of the table on vascular plants ecomorphs in the National Nature Park «Orelsky» (Baranovsky et al). The Belgard’s system of ecomorphs is particularly convenient and can be successfully applied to data processing in the ecological analysis of the flora on wide areas with significant species richness, and the proposed ecomorph will be another necessary element in the Belgard’s system of ecomorphs. 

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