Mineralization of the carbon and nitrogen of plant material added to soil and of the soil humus during incubation following periodic drying and rewetting of the soil

Summary The production of mineralized carbon and nitrogen by a slightly acid sandy loam soil, in the presence and absence of finely chopped fresh plant material or powdered dry plant material, was followed by determination of the amounts of carbon and nitrogen mineralized at intervals during continuous incubation over a period of twelve weeks. Mineralization of carbon and nitrogen was also followed in parallel soil samples and soil plant material mixtures which were dried at 35°C or 105°C and then rewetted every two weeks during the incubation period.The amounts of carbon and nitrogen mineralized were determined at intervals during the incubation period.Mineralization of the carbon and nitrogen of the humus of the soil was stimulated by periodic drying of the soil and particularly when the soil was dried at 105°C.It was found that more mineral nitrogen was produced from fresh plant material than from dried plant material in all the treatments. Periodic drying of the soil-plant material mixtures did not stimulate the production of mineral nitrogen from the added plant material and reduced it considerably when the drying was carried out at 105°C.Periodic drying at 35°C did not stimulate the mineralization of the carbon of fresh or dried plant material. It is clear therefore that, at temperatures occurring in nature, it is unlikely that the decomposition of plant material added to the soil will be stimulated as a consequence of drying of the soil. Periodic drying of the soil-plant material mixture at 105°C increased the mineralization of the carbon of the dried plant material. The amounts of carbon mineralized in 12 weeks from the dried plant material did not, however, exceed the amounts from fresh plant material incubated continuously in fresh soil or in soil periodically dried at 35°C.     

A sensitive and convenient assay for boron in plant using chromotropic acid and HPLC

A sensitive and convenient assay for boron (B) in plant material is reported. The assay involves extraction of B from plant material with dry ashing or 0.5M HCl, formation of a B-chromotropic acid (1,8-dihydroxynaphthalene-3, 6-disulfonic acid) complex in an aqueous solution, and determination of the complex on HPLC. Reliability of the assay was evaluated by analyzing a standard reference sample and satisfactory results were obtained. The proposed assay is applicable to dried plant material ccntaining 0.1 to 1 µg B, which is equivalent to a batch of 20 mg dried plant material containing B of 5 to 50 mg kg^-1.     

植物生根的分子机理研究进展

随着无性系育种在农林业上的广泛应用,其生根难的问题显得尤为突出。通过查阅相关文献,本文探讨了影响植物根发育的分子机理。从植物激素,主要从生长素调控植物根发育的分子机理;细胞周期相关基因影响植物根发育和与细胞壁形成相关的基因影响植物根发育等方面叙述了目前关于植物根发育的研究进展。并提出了解决研究生根分子机理材料难选择问题的方法。     

The Restoration Gene Pool Concept: Beyond the Native Versus Non-Native Debate

Abstract Restoration practitioners have long been faced with a dichotomous choice of native versus introduced plant material confounded by a general lack of consensus concerning what constitutes being native. The “restoration gene pool” concept assigns plant materials to one of four restoration gene pools (primary to quaternary) in order of declining genetic correspondence to the target population. Adaptation is decoupled from genetic identity because they often do not correspond, particularly if ecosystem function of the disturbed site has been altered. Because use of plant material with highest genetic identity, that is, the primary restoration gene pool, may not be ultimately successful, material of higher order pools may be substituted. This decision can be made individually for each plant species in the restored plant community in the scientific context that ecosystem management demands. The restoration gene pool concept provides a place for cultivars of native species and noninvasive introduced plant material when use of native‐site material is not feasible. The use of metapopulation polycrosses or composites and multiple‐origin polycrosses or composites is encouraged as appropriate. The restoration gene pool concept can be implemented as a hierarchical decision‐support tool within the larger context of planning seedings.     

A comparative study of isolation conditions,morphology, and properties of cellulose obtained from the stalks of cereals and oil-yielding plants

The impact of features of the capillary porous structure of rape and soya stalks (as compared with those of rye straw) on the nitric acid/alkaline delignification process allowing, in particular, isolation of radiation-free cellulose and nitrolignin from radionuclide-contaminated plant material, is examined. The method for adjustment of delignification conditions on changing from the traditional annual plant raw material (rye straw) to a material with a more dense structure of the plant tissue is discussed. The morphological structure and paper-forming properties of cellulose isolated from the stalks of cereals are shown to be identical with the respective indices for cellulose isolated from the stalks of oil-bearing plants.     

Partial purification and characterization of an insulin-like material from spinach and Lemna gibba G3

The existence in invertebrates, unicellular eukaryotes, and prokaryotes of materials that resemble several vertebrate peptide hormones led to the suggestion that these peptide messengers may have arisen earlier in evolution than had previously been thought. Consistent with this hypothesis, we describe here material in two plants, spinach and Lemma gibba G3, that is very similar to mammalian insulin, yet distinctive. In each of the early purification steps, which consisted of acidic methanol chloroform extraction and sequential chromatography on C-18 hydrophobic resin, Sephadex G-50, CM-Sepharose, and a short C-3 high performance liquid chromatography column, the immunoactive material from plants resembled the common vertebrate insulins. The protein nature of the material was suggested by its destruction by Pronase but not by the inactivated enzyme. In addition, on TSK chromatography it eluted in a position similar to that of insulin, i.e. equivalent to a protein of 6000 daltons. Using an isocratic high performance liquid chromatography system, the plant immunoactivity eluted earlier, and thus was more hydrophilic, than most of the common mammalian insulins, including pork insulin. The interaction of the plant material with anti-insulin antibodies in a radioimmunoassay was confirmed by using an affinity column of anti-insulin antibodies which adsorbed the plant immunoactivity at neutral pH, and released the material with acid elution. Using a quantitative double radioimmunoassay, the plant insulin-like material was distinguished immunologically from chicken insulin. Although the plant insulin-like material is clearly distinct from pork insulin chromatographically, and from chicken insulin immunologically, it resembles vertebrate insulins in its overall configuration. The plant insulin-like material bound to insulin receptors on IM-9 lymphocytes and stimulated glucose oxidation and lipogenesis in isolated adipocytes from young rats. The bioactivity was neutralized in the presence of anti-insulin antibodies, but not in the presence of normal guinea pig IgG. The role of this insulin-like material in plants is unknown but its existence is consistent with an early evolutionary origin of the insulin messenger peptide family. Alternatively we cannot exclude a later convergent development of this family or introduction of vertebrate DNA into plants.     

Silage studies IX biochemical changes in microbe-free silage

Summary If the aseptic plant material is regarded as a substrate for preservative microbial activity, it may be said that both the nitrogen and carbohydrate components undergo changes due to the influence of native enzymes in the plant material. These changes may very well be reflected in the microbial activity in a silage.It is interesting to compare the findings of this investigation, which show that during the days immediately after ensilage practically no changes take place when no bacteria are present. In a non-sterile ensilage, on the other hand, it is during this early stage that the briskest bacterial activity takes place.The chances of, say, an acid-forming microbial process actually lowering the pH in order that preservation of the material may take place are directly counteracted by the action of native enzymes of the vegetable material. During the days immediately after ensilage, however, if other conditions are favourable, microbial activity may clearly determine the whole course of events, and may possibly even inactivate the processes of the plant material itself.As is evident from the experiments described above, the activities inherent in the ensiled material itself are of no mean proportions. Further study of the mutual relationship of the ensilage and the various microbial fractions is therefore particularly necessary in order to be able to understand a number of processes of fundamental importance in biological preservation of plant material.     

(Chemotaxonomic) Implications of Postharvest/Storage‐Induced Changes in Plant Volatile Profiles – the Case of Artemisia absinthium L. Essential Oil

The plant volatile profile and the essential‐oil chemical composition change during the storage of plant material. The objective of this study was to develop a mathematical model able to predict, explain, and quantify these changes. Mathematical equations, derived under the assumption that the essential oil contained within plant material could be treated as an ideal solution (Raoult's law), were applied for tracking of postharvest changes in the volatile profile of Artemisia absinthium L. (the essential oils were analyzed by GC‐FID and GC/MS). Starting from a specific chemical composition of an essential‐oil sample obtained from plant material after a short drying period (typically 5–10 d), and by using the equations derived from this model, one could easily predict evaporation‐induced changes in the volatile profile of the plant material. Based on the composition of the essential‐oil sample obtained after a given storage time t, it is possible to identify those components that were involved in chemical reactions, both as reactants and possible products. The established model even allowed the recognition of pairs of transformation, i.e., ‘daughter’ products and their ‘parent’ compounds. The obtained results highlight that the essential‐oil composition is highly dependent on the storage period of any plant material and urges caution in different types of phytochemical studies, especially chemotaxonomic ones, or practical application.     

Bionic Composite Material Simulating the Optical Spectra of Plant Leaves

Though many physical models have been proposed to simulate the spectra of plant leaves, there are few reports on the material simulation of plant leaves. In order to prepare a material that could simulate the reflectance spectra of plant leaves, the spectral reflectance characteristics of plant leaves and their forming mechanism were analyzed. The study indicated that the reflectance spectra of plant leaves exhibits four common characteristics, which were determined by the spongy inner structure and biochemical contents (chlorophyll, water) of plant leaves. In our procedure, the chlorophyll was concealed into the high-oxygen-barrier polyvinyl alcohol (PVA) film to improve its photostability, and the water was sealed into the bag of high-vapor-barrier polyvinylidene chloride (PVDC) to prevent its vaporization loss. Subsequently, taking the structures of plant leaves and petals as simulating models and considering the limits of PVA film and PVDC bag, a novel bionic composite material constituted with three layers was designed and prepared. The spectral tests and endurance experiment show that the bionic composite material exhibits almost the same reflectance spectrum with those of green leaves, and its spectrum changes little after sunlight treatment for three months, which proves a good sunlight endurance of this bionic composite material.     

Washing technique for monitoring mites in apple orchards

A shake-and-wash technique for monitoring the predatory phytoseiid mitesTyphlodromus pyri, Amblyseius finlandicus, and their prey,Panonychus ulmi, Tetranychus urticae andAculus schlechtendali in commercial apple orchards was developed. The removal and recovery of mites from leaves, shoots and spurs is based on agitating the plant material by hand in alcohol and subsequently removing the mites using a separating funnel. The mites are quickly killed and easily washed off the plant material, and are thus well preserved for further study. The technique is more efficient than directly counting the mites on plant material under a dissection microscope and can be easily employed both in the laboratory and in the field.     

Metabolic fingerprinting of Cannabis sativa L., cannabinoids and terpenoids for chemotaxonomic and drug standardization purposes

Cannabis sativa L. is an important medicinal plant. In order to develop cannabis plant material as a medicinal product quality control and clear chemotaxonomic discrimination between varieties is a necessity. Therefore in this study 11 cannabis varieties were grown under the same environmental conditions. Chemical analysis of cannabis plant material used a gas chromatography flame ionization detection method that was validated for quantitative analysis of cannabis monoterpenoids, sesquiterpenoids, and cannabinoids. Quantitative data was analyzed using principal component analysis to determine which compounds are most important in discriminating cannabis varieties. In total 36 compounds were identified and quantified in the 11 varieties. Using principal component analysis each cannabis variety could be chemically discriminated. This methodology is useful for both chemotaxonomic discrimination of cannabis varieties and quality control of plant material.     

A simple,chisel-assisted mechanical microdissection system for harvesting homogenous plant tissue suitable for the analysis of nucleic acids and proteins

Many physiological processes are limited to specific tissues or even specific cell types. Analysing entire plants or organs results in averaged data of all cell types contained in the sample; thus, specific metabolic functions cannot be assigned to individual cell types. A higher spatial resolution is required. By microdissecting plant organs, homogeneous material can be obtained. If a suitable amount of material is collected, standard analytical methods can be applied to elucidate cell type-specific processes. The collection of sufficient quantities of homogeneous material can be done by means of mechanical microdissection. This technique is a low-cost alternative to laser-coupled microdissection techniques. Here we describe a protocol for chisel-assisted mechanical microdissection of embedded plant material and demonstrate that the collected material is suitable to obtain nucleic acids and proteins.     

ABA synthesis in protoplasts of different origin in response to osmotic stress

All the protoplasts analysed in this study whatever the original plant material were able to accumulate ABA under osmotic stress. The time course of ABA accumulation strongly differed according to the plant material. In both rose petal or Amaranthus leaf protoplasts, the increase in ABA level was significant but transient. Protoplasts prepared from Amaranthus cell suspensions behaved differently, showing a late and durable accumulation of ABA. Similar patterns of changes in ABA accumulation were observed in the original plant material under osmotic stress. A pretreatment of plant material by fluridone induced a strong inhibition of ABA accumulation whatever the origin of protoplasts was. This result suggests that ABA could be synthesised via the carotenoid pathway in the absence of the cell wall.     

Restoration of a species‐rich flood meadow by topsoil removal and diaspore transfer with plant material

Abstract. In previous studies, limited dispersal was revealed to be the main obstacle to restoration of species‐rich flood‐meadows along the northern Upper Rhine in Germany. To overcome dispersal limitation we transferred freshly mown plant material from species‐rich sources to a restoration site on a former arable field. Before plant material application, topsoil was removed to accelerate nutrient impoverishment and create favourable conditions for seedling recruitment. Topsoil removal led to a drastic reduction in organic matter and essential mineral nutrients to the level of target communities (P) or even below (N, K). At a removal depth of 30 cm content of the soil seed bank that comprised exclusively of annual arable weeds, ruderals and some common grassland species, declined by 60 ‐ 80%, while at a removal depth of 50 cm the seed bank was almost completely eliminated. With few exceptions, all species recorded in source plant material were found established at the restoration site. However, the overall correlation between seed content in plant material and establishment success was not very high. Vegetation development at the restoration site was characterized by a rapid decline in arable weeds and ruderals, while resident grassland species and species transferred with plant material increased rapidly from the third year onwards. After four years as many as 102 species were established that could be exclusively attributed to plant material transfer, among them many rare and highly endangered plants. Establishment of species from plant material was most successful in regularly flooded plots, due to the suppression of competitors as well as the creation of favourable moisture conditions for seedling emergence. Diaspore transfer with plant material proved to be an extremely successful method in restoring species‐rich grassland. However, high quality of plant material and suitable site conditions with low competition in early stages of succession seem to be essential prerequisites.     

Evaluation of Analytical Techniques to Predict Viability after Cryopreservation

Preservation of plant germplasm is important to safeguard biodiversity and to store elite plants. Cryopreservation is one of the possible preservation techniques. Research for a cryopreservation protocol is often inefficient because of slow or poor regrowth of plant material. Therefore, at least one technique, that allows a quick and accurate prognosis of viability after cryopreservation, is required. We evaluated five techniques: electrolyte leakage, triphe-nyltetrazoliumchloride (TTC) staining (visual and spectrophotometrical analysis), malondialdehyde concentrations in plant tissue and a mathematical model that relates ‘water content’ to the weight of encapsulated plant material. Electrolyte leakage and TTC-staining (if visually analysed) are efficient to predict viability. Our mathematical model allows us to save time and plant material in order to develop an efficient encapsulation—dehydration protocol. All other techniques were rejected because of the high variability of the results. This is due to the variability of biochemical activity in plant tissue and the small amount of tissue used in the experiments.     

The bug in a teacup—monitoring arthropod–plant associations with environmental DNA from dried plant material

Environmental DNA analysis (eDNA) has revolutionized the field of biomonitoring in the past years. Various sources have been shown to contain eDNA of diverse organisms, for example, water, soil, gut content and plant surfaces. Here we show that dried plant material is a highly promising source for arthropod community eDNA. We designed a metabarcoding assay to enrich diverse arthropod communities while preventing amplification of plant DNA. Using this assay, we analysed various commercially produced teas and herbs. These samples recovered ecologically and taxonomically diverse arthropod communities, a total of over a thousand species in more than 20 orders, many of them specific to their host plant and its geographical origin. Atypically for eDNA, arthropod DNA in dried plants shows very high temporal stability, opening up plant archives as a source for historical arthropod eDNA. Considering these results, dried plant material appears excellently suited as a novel tool to monitor arthropods and arthropod–plant interactions, detect agricultural pests and identify the geographical origin of imported plant material. The simplicity of our approach and the ability to detect highly diverse arthropod communities from all over the world in tea bags also highlights its utility for outreach purposes and to raise awareness about biodiversity.     

Bacterial secondary production on vascular plant detritus: relationships to detritus composition and degradation rate.

Bacterial production at the expense of vascular plant detritus was measured for three emergent plant species (Juncus effusus, Panicum hemitomon, and Typha latifolia) degrading in the littoral zone of a thermally impacted lake. Bacterial secondary production, measured as tritiated thymidine incorporation into DNA, ranged from 0.01 to 0.81 microgram of bacterial C mg of detritus-1 day-1. The three plant species differed with respect to the amount of bacterial productivity they supported per milligram of detritus, in accordance with the predicted biodegradability of the plant material based on initial nitrogen content, lignin content, and C/N ratio. Bacterial production also varied throughout the 22 weeks of in situ decomposition and was positively related to the nitrogen content and lignin content of the remaining detritus, as well as to the temperature of the lake water. Over time, production was negatively related to the C/N ratio and cellulose content of the degrading plant material. Bacterial production on degrading plant material was also calculated on the basis of plant surface area and ranged from 0.17 to 1.98 micrograms of bacterial C cm-2 day-1. Surface area-based calculations did not correlate well with either initial plant composition or changing composition of the remaining detritus during decomposition. The rate of bacterial detritus degradation, calculated from measured production of surface-attached bacteria, was much lower than the actual rate of weight loss of plant material. This discrepancy may be attributable to the importance of nonbacterial organisms in the degradation and loss of plant material from litterbags or to the microbially mediated solubilization of particulate material prior to bacterial utilization, or both.     

A new technique for studying the stylet tracks of homopteran insects in hand-sectioned plant tissue using light or epifluorescence microscopy

Homopteran insects, such as aphids, psyllids and scales, inject a proteinaceous salivary sheath into their host plant tissue during feeding. This sheath, also referred to as a stylet track, remains in the tissue after the stylets are withdrawn, and is useful for studying plant resistance to insects and plant virus transmission. We describe a new method for studying stylet tracks. Hand microtome sectioned plant material was fixed and cleared in ethanol. The stylet tracks were stained with acid fuchsin and counterstained with aniline blue or fast green. The acid fuchsin stained stylet tracks were pink to red under light microscopy, and orange under TRITC epifluorescence. Stylet tracks in unstained sections autofluoresced under DAPI epifluorescence. This new technique is significantly faster and less complex than previous techniques, and permitted visualization of stylet tracks with light or epifluorescence microscopy within 1 hr of collecting fresh plant material. The technique was also applicable to a broad range of homopterans and plant taxa and provided excellent photomicrographs.     

A new technique for studying the stylet tracks of homopteran insects in hand-sectioned plant tissue using light or epifluorescence microscopy

Homopteran insects, such as aphids, psyllids and scales, inject a proteinaceous salivary sheath into their host plant tissue during feeding. This sheath, also referred to as a stylet track, remains in the tissue after the stylets are withdrawn, and is useful for studying plant resistance to insects and plant virus transmission. We describe a new method for studying stylet tracks. Hand microtome sectioned plant material was fixed and cleared in ethanol. The stylet tracks were stained with acid fuchsin and counterstained with aniline blue or fast green. The acid fuchsin stained stylet tracks were pink to red under light microscopy, and orange under TRITC epifluorescence. Stylet tracks in unstained sections autofluoresced under DAPI epifluorescence. This new technique is significantly faster and less complex than previous techniques, and permitted visualization of stylet tracks with light or epifluorescence microscopy within 1 hr of collecting fresh plant material. The technique was also applicable to a broad range of homopterans and plant taxa and provided excellent photomicrographs.