Monitoring carbon stocks in the tropics and the remote sensing operational limitations: from local to regional projects.

Current remote sensing technologies are effective tools for contributing to the estimation of terrestrial carbon stocks and carbon stock changes. This paper provides an overview of information requirements, sensor capabilities and limitations, and analysis approaches for the use of remotely sensed data in the generation of tropical carbon sequestration monitoring systems. While it is evident that remotely sensed data have tremendous utility for monitoring carbon stock changes, it is important to be aware of their limitations. Three critical limitations are: (1) the definition of methods and algorithms to accurately estimate forest age, (2) the provision of techniques that can yield accurate estimation of deforestation rates in both tropical dry and wet forest environments, and (3) the strong need to develop new approaches to link biophysical variables (e.g., leaf area index) to spectral reflectance to support spatially distributed carbon sequestration models. The validity of final estimates of carbon and carbon stock changes rests on complex issues at several levels, from the data themselves, to the analysis, interpretation, and validation of the data. Consideration of these issues, as well as the need for sound project planning and development within budget constraints, will be important in the development of carbon stock monitoring programs in the tropics.

The influence of noise exposure on the parameters of a convolution model of the compound action potential.

The influence of noise exposure on the parameters of a convolution model of the compound action potential (CAP) was examined. CAPs were recorded in normal-hearing gerbils and in gerbils exposed to a 117 dB SPL 8 kHz band of noise for various durations. The CAPs were fitted with an analytic CAP to obtain the parameters representing the number of nerve fibers (N), the probability density function [P(t)] from a population of nerve fibers, and the single-unit waveform [U(t)]. The results showed that the analytic CAP fitted the physiologic CAPs well with correlations of approximately 0.90. A subsequent analysis using hierarchical linear modeling quantified the change in the parameters as a function of both signal level and hearing threshold. The results showed that noise exposure caused some of the parameter-level functions to simply shift along the signal level axis in proportion to the amount of hearing loss, whereas others shifted along the signal level axis and steepened. Significant changes occurred in the U(t) parameters, but they were not related to hearing threshold. These results suggest that noise exposure alters the physiology underlying the CAP, some of which can be explained by a simple lack of gain, whereas others may not.

Nuclear crystalloids in sieve elements of Boraginaceae: a protein digestion study.

Nuclear crystalloids have been found in sieve elements of several Boraginaceae. Nuclei of differentiating sieve elements of Echium and other genera except Amsinckia contain one or more crystalloids composed of thin rods densely packed in parallel arrangement. After the nuclei disintegrate in the maturing sieve element the crystalloids are released into the cell lumen where they persist intact. In Amsinckia the crystalloid consists of two components: a dense component, similar to the crystalloid in the other genera and a loosely arranged paracrystalline component. The proteinaceous nature of the nuclear crystalloids and their possible similarity to P-protein was investigated by enzyme digestion techniques. Three proteolytic enzymes were employed in this study: protease, pepsin and trypsin. Successful digestion of the dense crystalloid in both Echium and Amsinckia was obtained with each enzyme tested. P-protein plugging the sieve plate pores was also digested. The loose component in Amsinckia and the aggregated and dispersed P-protein were not affected by the enzyme digestion procedures. These results seemed to indicate that the density or compactness of the proteinaceous inclusions may play a role in the differential response.

Ultrastructure of potato leaf phloem infected with potato leafroll virus.

Electron microscopy of Russet Burbank potato (Solanum tuberosum L.) leaf midveins infected with the potato leafroll virus (PLRV) revealed the pathological effects induced by the virus in the phloem. Virus particles were observed in mature sieve elements, companion cells, and plasmodesmata connecting the two kinds of cells. An early indication of virally induced cellular disturbance in companion cells was dilation of mitochondrial cristae followed closely by the appearance of vesicles in the parietal cytoplasm. One type of vesicle contained fibrils suggestive of nucleic acids and the second type carried an electron opaque material. Both types of vesicles were surrounded by two membranes. Rough endoplasmic reticulum (ER) formed the outer membrane. Both vesicle types fused with the nuclear envelope and were taken up into the nucleus. PLRV particles appeared mainly in the cytoplasm, where they were either scattered or localized along the membranes of mitochondria, chloroplasts, and vacuoles. In some cells, groups of particles were enclosed in the vacuole. The relation of virus particles to the nucleus remains problematic: there was no evidence that uptake of vesicles into the nucleus resulted in the formation of particles in this organelle. Cells in which particles formed became degenerated. Mitochondria swelled and cristae separated from the envelope and clumped. Most organelles including the nucleus, ribosomes, rough ER, and chloroplasts broke down leaving a fibrillar material interspersed with virus particles.

Beet yellow stunt virus in cells of Sonchus oleraceus L. and its relation to host mitochondria.

In Sonchus oleraceus L. (Asteraceae) infected with the beet yellow stunt virus (BYSV) the virions are found in phloem cells, including the sieve elements. In parenchymatous phloem cells, the virus is present mainly in the cytoplasm. In some parenchymatous cells, containing massive accumulations of virus, the flexuous rodlike virus particles are found partly inserted into mitochondrial cristae. The mitochondrial envelope is absent where virus is present in the cristae. A similar relation between virus and host mitochondria apparently has not been recorded for any other plant virus.

A crystalline inclusion in sieve element nuclei of Amsinckia. I. The inclusion in differentiating cells.

The presence of usually single, elongated, compound crystalloids in nuclei of sieve elements is an outstanding characteristic of the phloem of Amsinckia douglasiana A. DC. (Boraginaceae). The crystalloid consists of two components forming alternating panels, or blocks, that extend through the entire length of the crystalloid and radiate from the centre where one of the components predominates. Three to seven panels for each component were recorded. One component consists of 4-sided tubules closely packed in highly ordered aggregates, the other of wider 6-sided tubules rather loosely arranged in paracrystalline aggregates. The crystalloid arises at the beginning of sieve element differentiation. Aggregates of 4-sided tubules appear first. In plants infected with the curly top virus, the crystalloids do not differ from those in non-infected controls in structure and conformation. But because the phloem in infected plants is hyperplastic, with most of the cells differentiating as sieve elements, the crystalloids are far more abundant in diseased than in healthy plants.

A crystalline inclusion in sieve element nuclei of Amsinckia. II. The inclusion in maturing cells.

The compounds crystalloids formed in sieve element nuclei of Amsinckia douglasiana A. DC. (Boraginaceae) during differentiation of the cell become disaggregated during the nuclear breakdown characteristic of a maturing sieve element. The phenomenon occurs in both healthy and virus-infected plants. The crystalloid component termed cy, which is loosely aggregated, separates from the densely aggregated component termed cx and disperses. The cx component may become fragmented, or broken into large pieces, or remain intact after the cell matures. After their release from the nucleus both crystalloid components become spatially associated with the dispersed P-protein originating in the cytoplasm, but remain distinguishable from it. The component tubules of P-protein are hexagonal in transections and are somewhat wider than the 6-sided cy tubules. The cx tubules are much narrower than the P-protein or the cy tubules and have square transections. Both the P-protein and the products of disintegrated crystalloids accumulate at sieve plates in sieve elements subjected to sudden release of hydrostatic pressure by cutting the phloem. The question of categorizing the tubular components of the nuclear crystalloid of a sieve element with reference to the concept of P-protein is discussed.

An ultrastructural study of acid phosphatase localization in Phaseolus vulgaris xylem by the use of an azo-dye method.

The localization of acid phosphatase during xylem development has been examined in the bean, Phaseolus vulgaris. The azo dye, the final reaction product, is initially prominent in the dictyosomes, vesicles apparently participating in secondary wall formation, and in the middle lamella of the young vessel element. Final reaction particles are also present in mitochondria, chloroplasts, and certain vacuoles and are sparsely scattered in the cytoplasm. At a later stage of vessel differentiation, the azo dye is concentrated in the disintegrating cytoplasm and along the fibrils of the partially hydrolysed primary wall and middle lamella. In the mature vessel element, the azo dye is still present along the disintegrated primary wall at the side of the vessel and covers the secondary wall. In the parenchyma cell adjacent to the vessel element, acid phosphatase localization is found in the dictyosomes, endoplasmic reticulum, mitochondria, small vacuoles, and the middle lamella. The controls from all stages of vessel element development were free of azo dye particles. The concentration of acid phosphatase along the secondary walls of the mature vessels and in the middle lamella between other cells indicates that this enzyme has other functions besides autolysis of the cytoplasm and primary cell wall. Acid phosphatase may participate in the formation of the secondary wall and may also have a role in the secretion and transport of sugars.

An ultrastructural study of acid phosphatase localization in cells of Phaseolus vulgaris phloem by the use of the azo dye method.

The localization of acid phosphatase was studied in the sieve elements and companion cells in the phloem tissue of the bean, Phaseolus vulgaris L. The various organelles in the two kinds of cell showed fine granules of the azo dye as the final reaction product. The aggregated smooth endoplasmic reticulum displayed the dye particularly consistently. The dye was also present in the plasmodesmata and in the contents of the sieve plate pores. The reaction product was conspicuous in the cell walls and tended to be concentrated in the middle lamella and in the nacreous wall layer of the differentiating sieve elements.