Vesicular-arbuscular mycorrhizal inoculum potential affects the growth of Stryphnodendron microstachyum seedlings in a Costa Rican human tropical lowland

This study used a plant bioassay to investigate the vesicular-arbuscular mycorrhizal (VAM) inoculum potential of soil from three vegetation types (fern, secondary forest, and grass) in an abandoned pasture in the tropical humid lowlands at La Selva, in northeastern Costa Rica. Growth, measured as seedling height, number of leaves, and total (above- and belowground) biomass, of Stryphnodendron microstachyum Poepp. et Endl. (Synon. S. excelsum Harms) seedlings was significantly lower when grown in soil inoculum from the fern areas than in soil inoculum from the forest and grass areas. However, S. microstachyum seedlings grown in the fern inoculum had significantly greater VAM colonization than seedlings grown in the forest and grass inoculum. In addition, roots collected from a dominant plant species from each of the three vegetation types showed that the fern (Nephrolepsis biserrata) had significantly greater mycorrhizal colonization than the tree (Pentaclethra macroloba (Willd.) Kuntze or the grass (Brachiaria spp.). The results of this study suggest that differences in mycorrhizal inoculum potential among vegetation types and its effects on seedling growth may have important implications for the restoration and management of degraded lands.     

Review of root dynamics in forest ecosystems grouped by climate,climatic forest type and species

Patterns of both above- and belowground biomass and production were evaluated using published information from 200 individual data-sets. Data sets were comprised of the following types of information: organic matter storage in living and dead biomass (e.g. surface organic horizons and soil organic matter accumulations), above- and belowground net primary production (NPP) and biomass, litter transfers, climatic data (i.e. precipitation and temperature), and nutrient storage (N, P, Ca, K) in above- and belowground biomass, soil organic matter and litter transfers. Forests were grouped by climate, foliage life-span, species and soil order. Several climatic and nutrient variables were regressed against fine root biomass or net primary production to determine what variables were most useful in predicting their dynamics. There were no significant or consistent patterns for above- and belowground biomass accumulation or NPP change across the different climatic forest types and by soil order. Similarly, there were no consistent patterns of soil organic matter (SOM) accumulation by climatic forest type but SOM varied significantly by soil order—the chemistry of the soil was more important in determining the amount of organic matter accumulation than climate. Soil orders which were high in aluminum, iron, and clay (e.g. Ultisols, Oxisols) had high total living and dead organic matter accumulations-especially in the cold temperate zone and in the tropics. Climatic variables and nutrient storage pools (i.e. in the forest floor) successfully predicted fine root NPP but not fine root biomass which was better predicted by nutrients in litterfall. The importance of grouping information by species based on their adaptive strategies for water and nutrient-use is suggested by the data. Some species groups did not appear to be sensitive to large changes in either climatic or nutrient variables while for others these variables explained a large proportion of the variation in fine root biomass and/or NPP.     

Synchronous fire activity in the tropical high Andes: an indication of regional climate forcing

Global climate models suggest enhanced warming of the tropical mid and upper troposphere, with larger temperature rise rates at higher elevations. Changes in fire activity are amongst the most significant ecological consequences of rising temperatures and changing hydrological properties in mountainous ecosystems, and there is a global evidence of increased fire activity with elevation. Whilst fire research has become popular in the tropical lowlands, much less is known of the tropical high Andean region (>2000masl, from Colombia to Bolivia). This study examines fire trends in the high Andes for three ecosystems, the Puna, the Paramo and the Yungas, for the period 1982–2006. We pose three questions: (i) is there an increased fire response with elevation? (ii) does the El Niño‐ Southern Oscillation control fire activity in this region? (iii) are the observed fire trends human driven (e.g., human practices and their effects on fuel build‐up) or climate driven? We did not find evidence of increased fire activity with elevation but, instead, a quasicyclic and synchronous fire response in Ecuador, Peru and Bolivia, suggesting the influence of high‐frequency climate forcing on fire responses on a subcontinental scale, in the high Andes. ENSO variability did not show a significant relation to fire activity for these three countries, partly because ENSO variability did not significantly relate to precipitation extremes, although it strongly did to temperature extremes. Whilst ENSO did not individually lead the observed regional fire trends, our results suggest a climate influence on fire activity, mainly through a sawtooth pattern of precipitation (increased rainfall before fire‐peak seasons (t‐1) followed by drought spells and unusual low temperatures (t0), which is particularly common where fire is carried by low fuel loads (e.g., grasslands and fine fuel). This climatic sawtooth appeared as the main driver of fire trends, above local human influences and fuel build‐up cyclicity.     

Seasonal patterns in depth of water uptake under contrasting annual and perennial systems in the Corn Belt Region of the Midwestern U.S.

In agricultural landscapes, variation and ecological plasticity in depth of water uptake by annual and perennial plants is an important means by which vegetation controls hydrological balance. However, little is known about how annual and perennial plants growing in agriculturally dominated landscapes in temperate humid regions vary in their water uptake dynamics. The primary objective of this study was to quantify the depth of water uptake by dominant plant species and functional groups growing in contrasting annual and perennial systems in an agricultural landscape in Central Iowa. We used stable oxygen isotope techniques to determine isotopic signatures of soil water and plant tissue to infer depth of water uptake at five sampling times over the course of an entire growing season. Our results suggest that herbaceous species (Zea mays L., Glycine max L. Merr., Carex sp., Andropogon gerardii Vitman.) utilized water predominantly from the upper 20 cm of the soil profile and exhibited a relatively low range of ecological plasticity for depth of water uptake. In contrast, the woody shrub (Symphoricarpos orbiculatus Moench.) and tree (Quercus alba L.) progressively increased their depth of water uptake during the growing season as water became less available, and showed a high degree of responsiveness of water uptake depth to changes in precipitation patterns. Co-existing shrubs and trees in the woodland and savanna sites extracted water from different depths in the soil profile, indicating complementarity in water uptake patterns. We suggest that deep water uptake by perennial plants growing in landscapes dominated by rowcrop agriculture can enhance hydrologic functioning. However, because the high degree of ecological plasticity allows some deep-rooted species to extract water from surface horizons when it is available, positive effects of deep water uptake may vary depending on species’ growth patterns and water uptake dynamics. Knowledge about individual species’ and plant communities’ depth of water uptake patterns in relation to local climate conditions and landscape positions can provide valuable information for strategically incorporating perennial plants into agricultural landscapes to enhance hydrologic regulation.     

Roots,nutrients and their relationship to spatial patterns

Ecosystem sustainability and resilience after a disturbance may be regulated by processes occurring at smaller spatial scales. The matrix of different spatial environments are created by (1) individual plants that accumulate higher concentrations of specific nutrients, trace elements or defensive plant secondary chemicals and thereby modify the chemistry of their ecological space and/or rates of processes, (2) the presence of structures (e.g., coarse woody debris) that may buffer some micro-environments from disturbances by functioning as a hospitable environment or as a reservoir for mycorrhizal fungi to sustain them into the next phase of stand development, and (3) chemical changes in soils during soil development which may result in distinct soil chemical environments. The response of the plants or change in the sustainability of carbon and nutrient cycles may be expressed more strongly at this smaller ecological space of an individual plant and furthermore must be frequently examined separately by the above- and belowground space of that individual.This paper will present three case studies from temperate and tropical forest ecosystems which suggest the importance of studying plant growth and nutrient and trace element cycling by stratifying sampling to encompass the mosaic patterns of existing spatial variability within the ecosystem. The examples show how individual plant species are able to create ecologically distinct spatial environments because of their distribution patterns within the landscape, how nutrient transfers in roots respond to the chemical variations in the soil, and how roots and mycorrhizal fungi are able to maintain themselves in the mosaic of coarse woody debris remaining on a site after the elimination of aboveground tree biomass.     

Drought effects on fine-root and ectomycorrhizal-root biomass in managed Pinus oaxacana Mirov stands in Oaxaca, Mexico

The effects of a severe drought on fine-root and ectomycorrhizal biomass were investigated in a forest ecosystem dominated by Pinus oaxacana located in Oaxaca, Mexico. Root cores were collected during both the wet and dry seasons of 1998 and 1999 from three sites subjected to different forest management treatments in 1990 and assessed for total fine-root biomass and ectomycorrhizal-root biomass. Additionally, a bioassay experiment with P. oaxacana seedlings was conducted to assess the ectomycorrhizal inoculum potential of the soil for each of the three stands. Results indicated that biomasses of both fine roots and ectomycorrhizal roots were reduced by almost 60% in the drought year compared to the nondrought year. There were no significant differences in ectomycorrhizal and fine-root biomass between the wet and dry seasons. Further, the proportion of total root biomass consisting of ectomycorrhizal roots did not vary between years or seasons. These results suggest that both total fine-root biomass and ectomycorrhizal-root biomass are strongly affected by severe drought in these high-elevation tropical pine forests, and that these responses outweigh seasonal effects. Forest management practices in these tropical pine forests should consider the effects of drought on the capacity of P. oaxacana to maintain sufficient levels of ectomycorrhizae especially when there is a potential for synergistic interactions between multiple disturbances that may lead to more severe stress in the host plant and subsequent reductions in ectomycorrhizal colonization.     

The socioeconomic conditions determining the development, persistence, and decline of forest garden systems

There is a range of forest management systems between pure extraction and plantation systems. Such “intermediate systems” range from wild forests modified for increased production of selected products to anthropogenic forests with a high-density of valuable species growing within a relatively diverse and complex structure. These systems, classed here as “Forest Garden Systems” (FGS), have important socioeconomic and ecological benefits, and yet they have been largely overlooked by researchers, development practitioners, and policy makers. Based on case examples and the authors’ experience, this paper analyzes the socioeconomic and institutional factors that explain the development, persistence, and decline of FGS. These systems combine productivity and biodiversity values and are important components in the diverse economic systems of their managers. As such, the model warrants increased attention to protect existing values, to support the adaptation of existing systems to changing circumstances, and to inform the development of new models of integrated forest management