3 results
The Value of Natural Ecosystems: An Economic and Ecological Framework
- Edward G. Farnworth, Thomas H. Tidrick, Carl F. Jordan, Webb M. Smathers, Jr
-
- Journal:
- Environmental Conservation / Volume 8 / Issue 4 / Winter 1981
- Published online by Cambridge University Press:
- 24 August 2009, pp. 275-282
-
- Article
- Export citation
-
Ecosystem values, and the functional roles of ecosystems in providing goods and services for Man, have been subjects of increasing discussion and controversy among ecologists and economists in recent years. Economists have developed economic theory based on a market model, and price or value has been set in the marketplace. However, the market system cannot account for all possible values, and fails to account for goods and services for which no market, or only imperfect markets, exist.
These non-traded goods and services are termed nonmarket values, and are categorized in the scheme we have developed either as Value II (attributable or assignable values) or as Value III (intangible or non-assignable values). The true or total value of natural systems should include not only the market values (Value I) but also these two categories of non-market values whenever decisions are made about the alteration of natural systems. Usually, only market values are incorporated by decision-makers in the management strategies of natural systems, and as a result of their omission of non-market values, numerous natural systems are being degraded or destroyed through market-goods extraction.
The examples of market and non-market values of tropical moist forests, demonstrate the range of nonmarket goods and services provided by natural ecosystems. Excessive alteration and destruction of tropical forests for extraction of market goods, damages the integrity of the forests and reduces or destroys the capacity of these ecosystems to provide valuable non-market goods and services. One can measure the value of these non-market goods and services by calculating the cost of providing them through technology. By not accounting for the public goods provided by forests, overall sustained-yield potential of the public and private goods produced by the system is reduced. These non-market values need to be incorporated in decisions about the fate of natural systems.
An attempt has been made in this paper to establish a common understanding of value for both economists and ecologists. If the problems of value determination can be viewed with a joint understanding, the political process may be influenced to provide more efficient and wiser use of the products and services of natural systems.
Effects of the oral administration of the products derived from milk fermentation by kefir microflora on immune stimulation
- Gabriel Vinderola, Gabriela Perdigón, Jairo Duarte, Edward Farnworth, Chantal Matar
-
- Journal:
- Journal of Dairy Research / Volume 73 / Issue 4 / November 2006
- Published online by Cambridge University Press:
- 07 July 2006, pp. 472-479
- Print publication:
- November 2006
-
- Article
- Export citation
-
Nutritional status has a major impact on the immune system. Probiotic effects ascribed to fermented dairy products arise not only from whole microorganisms but also from metabolites (peptides, exopolysaccharides) produced during the fermentation. We recently demonstrated the immunomodulating capacity of kefir in a murine model. We now aimed at studying the immunomodulating capacity in vivo of the products derived from milk fermentation by kefir microflora (PMFKM) on the gut. BALB/c mice received the PMFKM for 2, 5 or 7 consecutive days. IgA+ and IgG+ cells were determined on histological slices of the small and large intestine. IL-4, IL-6, IL-10, IL-12, IFNγ and TNFα were determined in the gut, intestinal fluid and blood serum. IL-6 was also determined in the supernatant of a primary culture of small intestine epithelial cells challenged with PMFKM. PMFKM up-regulated IL-6 secretion, necessary for B-cell terminal differentiation to IgA secreting cells in the gut lamina propria. There was an increase in the number of IgA+ cells in the small and large intestine. The increase in the number of IgA+ cells was accompanied by an increase in the number of IL-4+, IL-10+ and IL-6+ cells in the small intestine. Effects of PMFKM in the large intestine were less widely apparent than the ones observed at the small intestine lamina propria. All cytokines that increased in the small intestine lamina propria, also did so in blood serum, reflecting here the immunostimulation achieved in the gut mucosa. We observed that the PMFKM induced a mucosal response and it was able to up and down regulate it for protective immunity, maintaining the intestinal homeostasis, enhancing the IgA production at both the small and large intestine level. The opportunity exists then to manipulate the constituents of the lumen of the intestine through dietary means, thereby enhancing the health status of the host.
Immunomodulating capacity of kefir
- Celso G Vinderola, Jairo Duarte, Deepa Thangavel, Gabriela Perdigón, Edward Farnworth, Chantal Matar
-
- Journal:
- Journal of Dairy Research / Volume 72 / Issue 2 / May 2005
- Published online by Cambridge University Press:
- 21 March 2005, pp. 195-202
- Print publication:
- May 2005
-
- Article
- Export citation
-
Kefir is a fermented milk produced by the action of lactic acid bacteria, yeasts and acetic acid bacteria, trapped in a complex matrix of polysaccharides and proteins. Beyond its inherent high nutritional value as a source of proteins and calcium, kefir has a long tradition of being regarded as good for health in countries where it is a staple in the diet. However, published human or animal feeding trials to substantiate this view are not numerous. The aim of this work was to determine the immunomodulating capacity of kefir on the intestinal mucosal immune response in mice and to demonstrate the importance of dose and cell viability on this response. BALB/c mice were fed with commercial kefir ad libitum (diluted 1/10, 1/50, 1/100 or 1/200) or pasteurized kefir (diluted 1/6, 1/10, 1/50, 1/100) for 2, 5 or 7 consecutive days. At the end of each feeding period, the bacterial translocation assay was performed in the liver. Small intestine structure was studied by haematoxilin-eosin staining and light microscopy. The number of IgA+ and IgG+ cells was also determined. For the functional doses chosen, cytokines (IL-2, IL-4, IL-6, IL-10, IL-12, TNF-α and IFN-γ) were determined. Kefir and pasteurized kefir were able to modulate the mucosal immune system in a dose-dependent manner. Kefir was administred 10-times more diluted than pasteurized kefir, but it induced an immunomodulation of similar magnitude, indicating the importance of cell viabilty. The results suggest that a Th1 response was controlled by Th2 cytokines induced by kefir feeding. Pasteurized kefir would induce both Th2 and Th1 responses. This is the first study in vivo regarding the mechanisms involved in the immunomodulating capacity of the oral administration of kefir containing viable or heat-inactivated bacteria at different doses.