Chemistry of preen gland secretions of passerines: different pathways to same goal? why?

Summary. Passeriformes is the largest order of birds and includes one third of the bird species of the world, living in very diverse habitats. We investigated the chemistry of preen gland secretions of some groups of passerines from temperate regions found in diverse microhabitats. Some of the common components were mixtures of homologous monoesters made up of long chain acids and alcohols. Individual species had characteristic distribution of esters and was unique to a given species, although there were some individual variations. We compared the composition of acids and alcohols that formed same molecular weight esters in different species and we found that the combination of acids and alcohols to arrive at same molecular compositions varied distinctly between species. To compare compositions of over all acids and alcohols that formed the esters, the representative samples of secretions from the individual species were transesterfied the produce methyl esters and alcohols. We found that there were distinct differences in number of acids and alcohols that produced the combination of homologous mixtures of esters. Also they differed both qualitatively and quantitatively. There were also seasonal differences in the secretion components. Thus though the intact mixtures of esters in individual species had some similarities, they were very complex mixtures and differed characteristically for individual species. Here we discuss possible causes for evolution of these variations. We suggest that the evolution in variation of preen gland secretion is probably due to selective pressures caused by ectosymbionts such as feather-mites and feather-chewing lice that live on feathers and probably feed on the secretions and surrounding environments     

Population-level variation in plant secondary chemistry,and the population biology of herbivores

Summary Modern population ecology is becoming increasingly spatially-explicit. For insect hervibores, spatial variation in plant quality is a critical component of distribution and abundance. We argue that populationlevel measurements of phytochemical variation among individual plants has not kept pace with recent developments in population ecology. With examples from our own work, we demonstrate the importance of spatial variation in plant chemistry for insect herbivores, and suggest that phytochemistry should play a central role in the development of any spatially-based ecological theory.     

ⅠA族和ⅡA族金属的消烟助燃效应及其理论

ⅠＡ三金属和ⅡＡ碱土金属元素是有灰型消烟助燃剂的功能元素，就各族内而言，这些ｓ区金属元素的消烟助燃效应与它们的热电离电离热成反比，此特征与烃火焰条件下碳烟生成的正离子机制有关，就两族间而言，ⅡＡ族金属的消烟助燃效应通常大于ⅠＡ族金属，该特征与ｓ区金属元素的火焰电离特性有关，在实质上，ｓ区金属元素的消烟助燃效应与它们在火焰条件下发生电离的活化能有关，基于碳烟生成的双途径模型，含ⅠＡ，ⅡＡ族金属消烟助     

Inter- and Intra-Annual Chemical Variability During the ice-Free Season in Lakes with Different Flushing Rates and Acid Deposition Histories

Quantifying chemical variability in different lake types is important for the assessment of both chemical and biological responses to environmental change. For monitoring programs that emphasize a large number of lakes at the expense of frequent samples, high variability may influence how representative single samples are of the average conditions of individual lakes. Intensive temporal data from long-term research sites provide a unique opportunity to assess chemical variability in lakes with different characteristics. We compared the intra- and inter-annual variability of four acidification related variables (Gran alkalinity, pH, sulphate concentration, and total base cation concentration) in four lakes with different flushing rates and acid deposition histories. Variability was highest in lakes with high flushing rates and was not influenced by historic acid deposition in our study lakes. This has implications for the amount of effort required in monitoring programs. Lakes with high flushing rates will require more frequent sampling intervals than lakes with low flushing rates. Consideration of specific lake types should be included in the design of monitoring programs.     

DETECTABILITY OF STEP TRENDS IN THE RATE OF ATMOSPHERIC DEPOSITION OF SULFATE1

A method is presented to assist policy makers in determining the combination of number of sampling stations and number of years of sampling necessary to state with a given probability that a step reduction in atmospheric deposition rates of a given magnitude has occurred at a pre-specified time. This pre-specified time would typically be the time at which a sulfate emission control program took effect, and the given magnitude of reduction is some percentage change in deposition rate one might expect to occur as a result of the emission control. In order to determine this probability of detection, a stochastic model of sulfate deposition rates is developed, based on New York State bulk collection network data. The model considers the effect of variation in precipitation, seasonal variations, serial correlation, and site-to-site (cross) correlation. A nonparametric statistical test which is well suited to detection of step changes in such multi-site data sets is developed. It is related to the Mann-Whitney Rank-Sum test. The test is used in Monte Carlo simulations along with the stochastic model to derive statistical power functions. These power functions describe the probability of detecting (α=0.05) a step trend in deposition rate as a function of the size of the step-trend, record length before and after the step-trend, and the number of stations sampled. The results show that, for an area the size of New York State, very little power is gained by increasing the number of stations beyond about eight. The results allow policy makers to determine the tradeoff between the cost of monitoring and time required to detect a step-trend of a given magnitude with a given probability.     

CHEMICAL COMPOSITION OF SOFTWATER FLORIDA LAKES AND THEIR SENSITIVITY TO ACID PRECIPITATION1

ABSTRACT: Based on alkalinity data for 596 lakes, 31 percent of Florida's 7300 lakes have < 100 μeq/l alkalinity and are sensitive to acid depostion. More than two-thirds of the lakes in 12 northern Florida counties fit this criterion. Increasing aluminum and decreasing nutrient and chlorophyll a concentrations were observed with decressing pH in a survery of 20 softwater lakes. Maximum measured aluminum values (100-150 μg/L) are below levels asociated with fish toxicity. Factor analysis showed that lake chemistry was related to three principal factors, representing three major processes: watershed weathering, acidification, and nutrient inputs. An acidification index defined as the difference between excess SO₄^2- and excess (Ca²⁺+Mg²⁺) accounted for 74 percent of the variance in lake pH. Comparison of historical (late 1950a) and present data for pH, alkalinity, and excess SO₄^2- indicated loss of alkalinity (>25 μeq/L) and increase in excess SO₄^2- (16-34 μeq/L) in several softwater lakes.     

ATMOSPHERIC CONTRIBUTIONS TO FOREST NUTRIENT CYCLING1

The atmosphere is a significant source of plant nutrients that partially replenishes losses due to timber harvesting. The relative importance of wet and dry deposition depends upon the specific nutrient and site. Nitrogen in bulk precipitation (wetfall and dryfall) is equivalent to at least 70 percent of the nitrogen incorporated annually in above-ground woody tissues of some temperate hardwood forests. Atmospheric sources of calcium and potassium supply between 20 and 40 percent of the nutrients sequestered in woody increments. Annual nutrient inputs in bulk precipitation can exceed removals associated with sawiog harvest over a rotation period. Atmospheric inputs of nitrogen are only slightly less than hydrologic losses immediately after timber harvesting. The deposition of nutrients is highly variable in both time and space; interpretations of nutrient inputs and forest management impacts require quantification of inputs for a variety of ecosystems over long periods of time.     

THE EFFECTS OF DEICING SALTS ON WATER CHEMISTRY IN PINHOOK BOG,INDIANA1

ABSTRACT: A five-year study was conducted to identify the effects of road salt intrusion on the water chemistry of Pinhook Bog following operation of an uncovered salt storage pile adjacent to the bog for ten years. A distinct pattern of elevated salt concentrations was observed in the interstitial waters of the surface peat that corresponded to observed alterations in the bog vegetation. Yearly mean salt concentrations as high as 468 mg/l sodium and 1215 mg/l chloride were recorded in the plant root zone of the peat mat. The salt concentrations decreased significantly each year from 1979 to 1981 throughout the impacted area. Some increases of a lesser magnitude occurred in 1982 and 1983. Analysis of salt movements suggested that vertical transport by water movement was responsible for concentration changes. The major declines in salt levels occurred in the spring following snowmelt and heavy precipitation events. Evapotranspiration during periods of drought resulted in the gradual increases in surface peat salt concentrations. Diverted highway runoff was shown to be the major continuing source of sodium chloride contamination and was the likely source of the elevated calcium, magnesium, potassium, bicarbonate, and pH levels also observed in the impacted area.     

CHEMISTRY OF MUD-WATER INTERFACE IN AN IMPOUNDMENT1

ABSTRACT: Lake Evergreen was investigated during the time of filling and thereafter for the change of water chemistry at the mud-water interface. The results show that aging or maturing occurs at the nascent stage of the impoundment history. There are many factors affecting concentration of chemical constituents at the interface. There are hydrologic changes such as wind and wave action, or water circulation which can influence all chemical parameters. There is also biological activity, which may involve changes in concentrations of silica, phosphate, alkalinity, pH, ammonium, Kjeldahl nitrogen, etc. An associated effect is the reduction of oxidation-reduction potential which in turn affects the concentration of manganese, etc. All these changes occur primarily in autumn. In late spring to summer, there are changes of nitrite and nitrate accompanied by changes in dissolved oxygen. A water chemistry model at the interface is illustrated.     

EFFECTS OF FOREST HERBICIDE APPLICATIONS ON STREAMWATER CHEMISTRY IN SOUTHWESTERN BRITISH COLUMBIA1

ABSTRACT: The herbicide glyphosate was applied to portions of two watersheds in southwestern British Columbia to kill vegetation that was competing with Pseudotsuga menziesii (Douglas-fir) plantations. This application had little significant effect on streamwater chemistry (K⁺, Na²⁺, Mg²⁺, Ca²⁺, Cl^-, NOs₃^-, NH₄⁺, PO4^3-, SO₄⁼, and SiO₂ concentrations, electrical conductivity, and pH) when vegetation cover in a watershed was reduced by 4%, but had significant (P>0.05) effects, which lasted for at least five years, when cover was reduced by 43%. In this case, most parameters increased in value following the application, with K⁺ and Mg²⁺ concentrations and pH values exhibiting the most prolonged increases and NO₃^- concentrations exhibiting the greatest percentage increases. Sulphate and dissolved SiO₂ concentrations decreased following the application. Streamwater chemical fluxes showed similar trends to concentrations except that changes in fluxes were less significant and no decreases were observed. Forest management induced losses of NO₃-N in streamwater during the first five post-treatment years in the study area decreased in the order: herbicide application (approximately 40 kg/ha) < clearcutting and slashburning (approximately 20 kg/ha) < clearcutting (approximately 10 kg/ha). In watersheds similar to those of the study area, herbicide application is likely to have a greater impact on streamwater chemistry, in general, than would clearcutting or clearcutting followed by slashburning.