Lack of Evidence for 3/4 Scaling of Metabolism in Terrestrial Plants

Scaling, as the translation of information across spatial, temporal, and organizational scales, is essential to predictions and understanding in all sciences and has become a central issue in ecology. A large body of theoretical and empirical evidence concerning allometric scaling in terrestrial individual plants and plant communities has been constructed around the fractal volume-filling theory of West, Brown, and Enquist （the WBE model）. One of the most thought-provoking findings has been that the metabolic rates of plants, like those of animals, scale with their size as a 3/4 power law. The earliest, single most-important study cited in support of the application of the WBE model to terrestrial plants claims that whole-plant resource use in terrestrial plants scales as the 3/4 power of total mass, as predicted by the WBE model. However, in the present study we show that empirical data actually do not support such a claim. More recent studies cited as evidence for 3/4 scaling also suffer from several statistical and data-related problems. Using a forest biomass dataset including 1 266 plots of 17 main forest types across China, we explored the scaling exponents between tree productivity and tree mass and found no universal value across forest stands. We conclude that there is not sufficient evidence to support the existence of a single constant scaling exponent for the metabolism-biomass relationship for terrestrial plants.     

Evidence for a Mass Dependent Step-Change in the Scaling of Efficiency in Terrestrial Locomotion

A reanalysis of existing data suggests that the established tenet of increasing efficiency of transport with body size in terrestrial locomotion requires re-evaluation. Here, the statistical model that described the data best indicated a dichotomy between the data for small (<1 kg) and large animals (>1 kg). Within and between these two size groups there was no detectable difference in the scaling exponents (slopes) relating metabolic (E _met) and mechanical costs (E _{mech, CM}) of locomotion to body mass (M _b). Therefore, no scaling of efficiency (E _{mech, CM}/E _met) with M _b was evident within each size group. Small animals, however, appeared to be generally less efficient than larger animals (7% and 26% respectively). Consequently, it is possible that the relationship between efficiency and M _b is not continuous, but, rather, involves a step-change. This step-change in the efficiency of locomotion mirrors previous findings suggesting a postural cause for an apparent size dichotomy in the relationship between E _met and M _b. Currently data for E _{mech, CM} is lacking, but the relationship between efficiency in terrestrial locomotion and M _b is likely to be determined by posture and kinematics rather than body size alone. Hence, scaling of efficiency is likely to be more complex than a simple linear relationship across body sizes. A homogenous study of the mechanical cost of terrestrial locomotion across a broad range of species, body sizes, and importantly locomotor postures is a priority for future research.     

Molybdenum Metabolism in Plants

Abstract: Among the micronutrients essential for plant growth and for microsymbionts, Mo is required in minute amounts. However, since Mo is often sequestered by Fe- or Al-oxihydrox-ides, especially in acidic soils, the concentration of the water-soluble molybdate anion available for uptake by plants may be limiting for the plant, even when the total Mo content of the soil is sufficient. In contrast to bacteria, no specific molybdenum uptake system is known for plants, but since molybdate and sulfate behave similarly and have similar structure, uptake of molybdate could be mediated unspecifically by one of the sulfate transporters. Transport into the different plant organs proceeds via xylem and phloem. A pterin-bound molybdenum is the cofactor of important plant enzymes involved in redox processes: nitrate reductase, xanthine dehydrogenase, aIdehyde oxidase, and probably sulfite oxidase. Biosynthesis of the molybdenum cofactor (Moco) starts with a guanosine-X-phos-phate. Subsequently, a sulfur-free pterin is synthesized, sulfur is added, and finally molybdenum is incorporated. In addition to the molybdopterin enzymes, small molybdopterin binding proteins without catalytic function are known and are probably involved in the storage of Moco. In symbiotic systems the nitrogen supply of the host plant is strongly influenced by the availability of Mo in soil, since both bacterial nitrogenase and NADPH-dependent nitrate reductase of mycorrhizal fungi are Mo enzymes.     

Physiological Diversity in Metabolism in Marine and Terrestrial Crustacea

Two aspects of metabolic adaptation to increased terrestrialismare considered: (1) respiratory adaptations as reflected bycomparative cytochrome c oxidase activity in tissues of crabsfrom aquatic and terrestrial habitats, and (2) thermal acclimationpatterns in cytochrome c oxidase activity in tissues from thesecrabs. Enzymatic assays were done spectrophotometrically ongill, muscle, and mid-gut gland tissues from two aquatic species,Libinia emarginata and Callinectes sapidus, and the terrestrialOcypode quadrata. Cytochrome c oxidase was chosen for this studysince it is generally believed that the more aerobic the cellsor tissues become, the more fully developed the cytochrome systemwill be. This enzyme is also thought to have a role in thermalacclimation. In gill tissue the activity of cytochrome c oxidase is enhancedwith the advent of aerial respiration. Enzymatic activity ofgill tissue from Ocypode quadrata was significantly greaterthan it was in tissue from the aquatic species. No correlationwas observed with increased terrestrialism and enzymatic activityof muscle or mid-gut gland tissue. The thermal acclimation patternsof tissues of these three species of crabs indicate a clear-cuttendency for less enzymatic adaptation to temperature at thetissue level as these crabs evolve toward a land habitat.     

高等植物中铁的代谢机制

铁在高等植物的生长发育中发挥着重要作用,但随着人类的耕作及土壤的盐碱化,缺铁已成为一个世界性植物营养问题。高等植物在长期的进化过程中,形成了完善的对环境铁信号响应的体系。本文围绕植物与环境的相互作用,综述了近年来植物铁营养的吸收、转运、分配和储存的研究进展,并总结了植物中铁营养代谢调控的相关机理。     

植物苯丙烷代谢途径

众所周知,固着生长的植物经常受到环境中各种生物和非生物胁迫的威胁。所以在漫长的进化过程中,植物必须将多样的环境信号整合到其发育过程中,以实现适应性形态的发生和代谢途径的精确调控,最终使植物完成整个生长周期。研究显示,苯丙烷代谢作为植物重要的次级代谢途径之一,其代谢产物,例如木质素、孢粉素、花青素和有机酸等,在调控植物适应性生长的过程中发挥着重要功能。特别是在药用植物中,苯丙烷代谢还与众多药用活性成分的合成息息相关,几乎所有包含苯丙烷骨架的天然药效成分均由苯丙烷代谢途径直接或间接合成,例如黄酮类、萜类和酚类等。此外,经苯丙烷代谢途径产生的一些次级代谢产物还能由植物根系外泌到周际土壤中,通过改变根系微生物的菌群生态,而影响植物生长和抵抗生物或非生物胁迫的能力。同时,苯丙烷代谢介导的这种植物-微生物互作也与药用植物的道地品质密不可分。本文综述了近年来植物苯丙烷代谢途径的最新研究进展,重点对该代谢途径中代谢产物的生理功能及表达调控机制进行了介绍,以期更深入地理解药用植物苯丙烷代谢与药材性状之间的潜在关系,旨在指导优良中草药的遗传育种,以进一步促进我国中医药事业的蓬勃发展。     

全球变化背景下陆地植物N/P生态化学计量学研究进展

生态化学计量学理论最早应用在水生生态系统的研究中,但最近20年来在陆地生态系统中也开展了大量的相关研究,特别是关于全球变化背景下陆地植物N/P生态化学计量学方面的研究得到很大的发展,极大地丰富和提升了我们对陆地植物包括生态系统生态过程的认识。就全球变化背景下陆地植物生态化学计量学的研究现状进行了综述,同时以中国科学院华南植物园90周庆为契机,总结我们关于南亚热带森林植物生态化学计量学的研究工作,进而分析当前存在的一些问题并提出今后研究的发展重点,以期促进和推动我园和我国生态化学计量学相关领域的研究。     

Nitrogen Metabolism in the Terrestrial Isopod, Oniscus asellus

The total diffusible content of ammonia in Oniscus asellus wasmeasured as 1.20 mg % body fluid. Daily excretions of ammoniaexceeded the total diffusible content in measurements on specimenstaken directly from nature. The content of uric acid in a groupof 35 specimens was 11.3 mg % body weight and 93% of this materialwas in the body wall. Urea was not measurable under conditionsthat would have allowed detection of at least 0.26 mg % bodyfluid. Only arginase of the enzymes in the ornithine-urea cycle wasmeasurable. Labeled urea was not detectable in aqueous extractsunder conditions where approximately 50,300 CPM of labeled carbonwas incorporated into metabolites. Labeled arginine was notdetectable under conditions where 9,100 CPM of KHC¹⁴O₃ wereincorporated into the soluble protein fraction and more than3,340,000 CPM were incorporated into particulate protein andnon-protein fractions of the organism. All of the enzymes of uricolysis to ammonia were present, uricaseand urease being rate-limiting. Uricase was measurable as myeloperoxidase.Although high rates of glutamate-oxalacetate aminotransferaseand glutamate-pyruvate aminotransferase were readily measured,glutamic dehydrogenase activity proceeded slowly, suggestingsynthesis of needed amino acids as the key function of the transaminaseactivities. Amino acid oxidase activities, glutaminase, and asparaginaseactivities were low, too, whereas peroxidatic deaminase activitiesproceeded at rates sufficiently fast to account for the levelsof volatile ammonia emitted in vivo. Although molting may serve for excretion of end-products ofpurine catabolism, no central organ homologous to kidney orliver appears to be present with respect to detoxication orexcretion of ammonia. Inasmuch as O. asellus is not exposed to osmotic stresses, doesnot ordinarily face problems of dehydration, and tolerates levelsof ammonia generally ascribed as toxic to other organisms, itis proposed that retention of ammonotelism probably offers thermodynamicadvantages to the organism. The evolution of a system whereinammonia is excreted as a gas may have provided the organismwith an adaptive mechanism for colonizing land.     

{gamma}-Aminobutyric Acid Metabolism in Plants: Part 2. Metabolism in Higher Plants

The metabolism of -aminobutyric acid (AB) has been studied inhigher plants, particularly in peas and peanuts. Transaminationappeared to form the first step in AB degradation although transaminaseactivities were very low. The relatively active AB transaminaseassociated with whole pea plants possessing nodulated rootsappears to reside almost entirely within the nodules. AB transaminationwas demonstrated conclusively in extracts of mitochondria fromcotyledons of peanut seedlings; pyruvic acid acted as a betteramino-group acceptor than -ketoglutaric acid (KG). AB transaminaseactivity present in the microsomal and soluble cytoplasmic fractionsof the cells was very low AB was not metabolized perceptibly by intact mitochondria frompeanut, but when various organic acids were supplied simultaneously,an extra uptake of oxygen occurred and was associated with ABdisappearance. Aspartate, alanine, and ammonia were formed usingthe nitrogen atom of AB. The metabolic pathway followed by the carbon skeleton of ABwas traced by supplying C¹⁴-labelled material to leaf discsof peas and to mitochondria from peanut cotyledons. Radioactivitywas incorporated into organic acids, amino-acids, and respiratorycarbon dioxide in a manner suggesting that AB was convertedinto succinate which was then metabolized by the enzymes ofthe Krebs cycle present in the plant mitochondria. Glutamic decarboxylase was shown to be present largely in thenon-particulate (soluble) cytoplasm of cells. The enzymes responsiblefor AB synthesis and degradation, glutamic decarboxylase, andAB transaminase, respectively, therefore largely reside in differentsub-cellular fractions.     

Cyanide Metabolism in Higher Plants: Cyanoalanine Hydratase is a NIT4 Homolog

Cyanoalanine hydratase (E.C. 4.2.1.65) is an enzyme involved in the cyanide detoxification pathway of higher plants and catalyzes the hydrolysis of β-cyano-l-alanine to asparagine. We have isolated the enzyme from seedlings of blue lupine (Lupinus angustifolius) to obtain protein sequence information for molecular cloning. In contrast to earlier reports, extracts of blue lupine cotyledons were found also to contain cyanoalanine-nitrilase (E.C. 3.5.5.4) activity, resulting in aspartic acid production. Both activities co-elute during isolation of cyanoalanine hydratase and are co-precipitated by an antibody directed against Arabidopsis thaliana nitrilase 4 (NIT4). The isolated cyanoalanine hydratase was sequenced by nanospray-MS/MS and shown to be a homolog of Arabidopsis thaliana and Nicotiana tabacum NIT4. Full-length cDNA sequences for two NIT4 homologs from blue lupine were obtained by PCR using degenerate primers and RACE-experiments. The recombinant LaNIT4 enzymes, like Arabidopsis NIT4, hydrolyze cyanoalanine to asparagine and aspartic acid but show a much higher cyanoalanine-hydratase activity. The two nitrilase genes displayed differential but overlapping expression. Taken together these data show that the so-called ‘cyanoalanine hydratase’ of plants is not a bacterial type nitrile hydratase enzyme but a nitrilase enzyme which can have a remarkably high nitrile-hydratase activity.     

Bioassays and Field Studies for Allelopathy in Terrestrial Plants: Progress and Problems

Bioassays are an integral part of allelopathy research. The unsuitability of laboratory bioassays to explain field situations is discussed previously. In this article, we discuss progress in bioassay experimental design and several unresolved problems associated with research on allelopathy. The objectives of this article are to discuss problems related to (1) collection of allelopathic material for bioassay, (2) allelochemical quantification in bioassays, (3) selection of concentration of allelochemicals in bioassay, (4) selection of appropriate control, (5) interaction between allelochemicals and other substances, and (6) in situ allelochemical bioassays. We concluded that new experimental designs for in situ bioassay are needed that can account for the large number of confounding factors in a complex field environment, and can be linked to physiological monitoring of target species and biochemical monitoring of the growth medium. Referee: Dr. Stella Elakovich, Dept. of Chemistry and Biochemistry, University of Southern Mississippi, Hattiesburg, MS 390406-5043     

植物的苹果酸代谢和转运

本文简要回顾了苹果酸代谢和转运的研究进展。     

Evidence for Central Regulation of Glucose Metabolism

Evidence for central regulation of glucose homeostasis is accumulating from both animal and human studies. Central nutrient and hormone sensing in the hypothalamus appears to coordinate regulation of whole body metabolism. Central signals activate ATP-sensitive potassium (K_ATP) channels, thereby down-regulating glucose production, likely through vagal efferent signals. Recent human studies are consistent with this hypothesis. The contributions of direct and central inputs to metabolic regulation are likely of comparable magnitude, with somewhat delayed central effects and more rapid peripheral effects. Understanding central regulation of glucose metabolism could promote the development of novel therapeutic approaches for such metabolic conditions as diabetes mellitus.