Nitrogen relations of the sorghum-Sfriga hermonthica hostparasite association: growth and photosynthesis

The extent to which the parasitic angiosperm Striga hermonthica reduces the growth of its sorghum host is dependent on the concentration of nitrogen (as NH₄NO₃ in 40% Long Ashton Solution) supplied to the plants. The biomass of 0.5,1 and 2 mol m^?3 N-grown infected plants was 22,30 and 66%, respectively, of uninfected plants after 140d growth. The biomass of 3 and 4 mol m^?3 N-grown infected plants differed little from uninfected plants. No grain was set in 0.5 and 1 mol m^?3 N-grown infected plants, grain yield reached 42 and 73% of controls in 2 and 3 mol m^?3 N-grown plants, and was unaffected in 4 mol m^?3 N-grown plants. Striga hermonthica also altered the allometry and architecture of the host, at all but the highest N concentration. Higher N concentration (3 and 4 mol m ^?3 N) reduced the growth of S. hermonthica. Foliar N concentrations in sorghum ranged from 11 mg g^?1 dwt. in 0.5 mol m^?3 N-grown plants, to 28 mg g^?1 dwt. in 4 mol m^?3 N-grown plants, and were not affected by S. hermonthica. Higher N concentrations were measured in S. hermonthica, and ranged from 18 to 45 mg g^?1 dwt. in 0.5 and 3 mol m^?3 N-grown plants, respectively. The relationship between photosynthesis (CO₂ flux) and N concentration differed between uninfected and infected sorghum. This was most apparent in 0.5 mol m^?3 N-grown plants, with rates of 16 and 11 μmol m^?2 s^?1 in uninfected and infected plants, respectively (at 1500–1800 μmol m^?2 s^?1 photosynthetic photon flux density). At higher N concentrations, this difference was smaller, with both sets of plants reaching 26 μmol m^?2 s^?1 at 4 mol m^?3 N. Varying the level of S. hermonthica infection showed that the effect of N on host photosynthesis cannot be explained by differences in the mass or number of parasites supported by the host. At low levels of infection in 1 mol m^?3 N-grown plants, the negative effect of the parasite was reversed, and photosynthesis in infected plants exceeded that in uninfected plants by 20%. Photosynthesis in S. hermonthica at 3 mol m^?3 N (8 μmol m^?2 s^?1) was double that in 0.5 mol m^?3 N-grown plants. Stable carbon isotope and gas exchange measurements data demonstrated that this higher level of autotrophic carbon fixation was accompanied by a lower dependency on hetero trophic carbon. The latter ranged from 27 to 6% in 0 5 mol m^?3 and 3 mol m^?3 N-grown plants, respectively.     

C4 plants in the vegetation of Mongolia: their natural occurrence and geographical distribution in relation to climate

The natural geographical occurrence, carbon assimilation, and structural and biochemical diversity of species with C₄ photosynthesis in the vegetation of Mongolia was studied. The Mongolian flora was screened for C₄ plants by using ¹³C/¹²C isotope fractionation, determining the early products of ¹⁴CO₂ fixation, microscopy of leaf mesophyll cell anatomy, and from reported literature data. Eighty C₄ species were found among eight families: Amaranthaceae, Chenopodiaceae, Euphorbiaceae, Molluginaceae, Poaceae, Polygonaceae, Portulacaceae and Zygophyllaceae. Most of the C4 species were in three families: Chenopodiceae (41 species), Poaceae (25 species) and Polygonaceae, genus Calligonum (6 species). Some new C₄ species in Chenopodiaceae, Poaceae and Polygonaceae were detected. C₄ Chenopodiaceae species make up 45% of the total chenopods and are very important ecologically in saline areas and in cold arid deserts. C₄ grasses make up about 10% of the total Poaceae species and these species naturally concentrate in steppe zones. Naturalized grasses with Kranz anatomy,of genera such as Setaria, Echinochloa, Eragrostis, Panicum and Chloris, were found in almost all the botanical-geographical regions of Mongolia, where they commonly occur in annually disturbed areas and desert oases. We analyzed the relationships between the occurrence of C₄ plants in 16 natural botanical-geographical regions of Mongolia and their major climatic influences. The proportion of C₄ species increases with decreasing geographical latitude and along the north-to-south temperature gradient; however grasses and chenopods differ in their responses to climate. The abundance of Chenopodiaceae species was closely correlated with aridity, but the distribution of the C₄ grasses was more dependent on temperature. Also, we found a unique distribution of different C₄ Chenopodiaceae structural and biochemical subtypes along the aridity gradient. NADP-malic enzyme (NADP-ME) tree-like species with a salsoloid type of Kranz anatomy, such as Haloxylon ammodendron and Iljinia regelii, plus shrubby Salsola and Anabasis species, were the plants most resistant to ecological stress and conditions in highly arid Gobian deserts with less than 100 mm of annual precipitation. Most of the annual C₄ chenopod species were halophytes, succulent, and occurred in saline and arid environments in steppe and desert regions. The relative abundance of C₃ succulent chenopod species also increased along the aridity gradient. Native C₄ grasses were mainly annual and perennial species from the Cynodonteae tribe with NAD-ME and PEP-carboxykinase (PEP-CK) photosynthetic types. They occurred across much of Mongolia, but were most common in steppe zones where they are often dominant in grazing ecosystems. Received: 17 March 1999 / Accepted: 1 November 1999     

C4 photosynthesis, atmospheric CO2, and climate

The objectives of this synthesis are (1) to review the factors that influence the ecological, geographical, and palaeoecological distributions of plants possessing C₄ photosynthesis and (2) to propose a hypothesis/model to explain both the distribution of C₄ plants with respect to temperature and CO₂ and why C₄ photosynthesis is relatively uncommon in dicotyledonous plants (hereafter dicots), especially in comparison with its widespread distribution in monocotyledonous species (hereafter monocots). Our goal is to stimulate discussion of the factors controlling distributions of C₄ plants today, historically, and under future elevated CO₂ environments. Understanding the distributions of C₃/C₄ plants impacts not only primary productivity, but also the distribution, evolution, and migration of both invertebrates and vertebrates that graze on these plants. Sixteen separate studies all indicate that the current distributions of C₄ monocots are tightly correlated with temperature: elevated temperatures during the growing season favor C₄ monocots. In contrast, the seven studies on C₄ dicot distributions suggest that a different environmental parameter, such as aridity (combination of temperature and evaporative potential), more closely describes their distributions. Differences in the temperature dependence of the quantum yield for CO₂ uptake (light-use efficiency) of C₃ and C₄ species relate well to observed plant distributions and light-use efficiency is the only mechanism that has been proposed to explain distributional differences in C₃/C₄ monocots. Modeling of C₃ and C₄ light-use efficiencies under different combinations of atmospheric CO₂ and temperature predicts that C₄-dominated ecosystems should not have expanded until atmospheric CO₂ concentrations reached the lower levels that are thought to have existed beginning near the end of the Miocene. At that time, palaeocarbonate and fossil data indicate a simultaneous, global expansion of C₄-dominated grasslands. The C₄ monocots generally have a higher quantum yield than C₄ dicots and it is proposed that leaf venation patterns play a role in increasing the light-use efficiency of most C₄ monocots. The reduced quantum yield of most C₄ dicots is consistent with their rarity, and it is suggested that C₄ dicots may not have been selected until CO₂ concentrations reached their lowest levels during glacial maxima in the Quaternary. Given the intrinsic light-use efficiency advantage of C₄ monocots, C₄ dicots may have been limited in their distributions to the warmest ecosystems, saline ecosystems, and/or to highly disturbed ecosystems. All C₄ plants have a significant advantage over C₃ plants under low atmospheric CO₂ conditions and are predicted to have expanded significantly on a global scale during full-glacial periods, especially in tropical regions. Bog and lake sediment cores as well as pedogenic carbonates support the hypothesis that C₄ ecosystems were more extensive during the last glacial maximum and then decreased in abundance following deglaciation as atmospheric CO₂ levels increased. Received: 12 February 1997 / Accepted: 20 June 1997     

Distribution of South African C3 and C4 species of Cyperaceae in relation to climate and phylogeny

Abstract In this study the contribution of climatic factors and phylogenetic relationships affecting the geographical distribution of C₃ and C₄ genera of the Cyperaceae in South Africa was investigated. The δ¹³C values of herbarium specimens of 68 southern African species from 22 genera and eight tribes were used to assign the species to either the C₃ or C₄ photosynthetic pathway. Geographical distribution data for the Cyperaceae were used to investigate relationships between climatic factors and the number of species and proportional abundance of C₄ species per region. The number of Cyperaceae species per 2° × 2° square across South Africa varied from less than five in the north‐western regions to more than 15 in the south‐western and north‐eastern regions of South Africa where rainfall exceeds 800 mm y^‐1. Of the 68 species investigated, 28 had C₄ photosynthesis and these were scattered among nine genera of four tribes (Cypereae, Scirpeae, Abildgaardieae and Rhyncosporeae). The proportional abundance of C₄ species ranged from 14% in the winter rainfall regions of the south‐west of South Africa to 67% in the summer rainfall areas of the north‐east. The geographical distribution of species was related to their phylogenetic position such that the distributions of C₃ and C₄ species in Cypereae, Scirpeae and Schoeneae was quite distinct. Linear regression analysis showed that the transition temperatures (equal C₃ and C₄ species numbers) for the Cyperaceae were different to those obtained for the Poaceae from the same region. No strong relationships were found between the proportional abundance of C₄ species and other climate factors such as altitude and rainfall. Our analysis of the current geographical distribution of C₄ Cyperaceae in southern Africa in a phylogenetic context suggests that the ecological advantages conferred by the C₄ pathway differ amongst the different plant groups.     

Climate and the U.S. distribution of C4 grass subfamilies and decarboxylation variants of C4 photosynthesis

I compared the C(4) grass flora and climatic records for 32 sites in the United States. Consistent with previous studies, I found that the proportion of the grass flora that uses the NADP malic enzyme (NADP-ME) variant of C(4) photosynthesis greatly increases with increasing annual precipitation, while the proportion using the NAD malic enzyme (NAD-ME) variant (and also the less common phosphoenolpyruvate carboxykinase [PCK] variant) decreases. However the association of grass subfamilies with annual precipitation was even stronger than for the C(4) decarboxylation variants. Analysis of the patterns of distribution by partial correlation analysis showed that the correlations between the frequency of various C(4) types and rainfall were solely due to the association of the C(4) types with particular grass subfamilies. In contrast, there was a strong correlation of the frequency of the different subfamilies with annual precipitation that was independent of the influence of the different C(4) variants. It therefore appears that other, as yet unidentified, characteristics that differ among grass subfamilies may be responsible for their differences in distribution across natural precipitation gradients.     

控温条件下C3、C4草本植物碳同位素组成对温度的响应

采取人工控制实验,探讨了6种C3、C4草本植物在昼/夜温度指标为20/12℃!36/28℃的范围内植物碳同位素组成(δ13C)及其对温度变化的响应,并结合植物比叶面积(SLA)、胞间CO2浓度(ci)与环境CO2浓度(ca)的比值、碳同化率(净光合速率Pn/胞间CO2浓度ci)等光合生长指标对植物δ13C的影响进行了分析。结果表明:所有C3、C4植物样品的δ13C值分别变化在-28.3‰!-32.1‰和-14.4‰!-17.6‰之间;在C3植物中,油菜δ13C值分布范围最集中,位于-31.1‰!-32.1‰之间;C4植物中,谷子δ13C值分布范围最窄。在控制的温度范围内,3种C3植物的平均δ13C值随温度升高而显著变低,而C4植物δ13C平均值与温度呈先增大后减小的抛物型关系,但线性回归结果未达到显著水平(P0.05)。单个植物种的δ13C值对温度的响应不同,茄子、高粱的δ13C值与温度呈线性负相关,其它4种植物与温度均呈二次抛物线关系,这可能与不同植物种具有不同的光合最适温度以及植物δ13C分馏对温度变化的敏感程度不同有关。     

C3 photosynthesis in Aristida longifolia: Implication for photosynthetic diversification in Aristidoideae (Poaceae)

Only a small percentage of plant species undergo C(4) photosynthesis. Despite its rarity, the C(4) pathway has evolved numerous times from C(3) ancestors, with as many as 18 independent origins in grasses alone. We report non-Kranz (C(3)) anatomy in Aristida longifolia, a species in a genus of ca. 300 species previously thought to possess only Kranz (C(4)) anatomy. Leaf blade transections of A. longifolia show widely spaced vascular bundles, nonradiate chlorenchyma, and few or no chloroplasts in cells of the sheaths surrounding the vascular bundle, all features indicative of C(3) photosynthesis. Carbon isotope ratios range from -27.68 to -29.71%, likewise indicative of C(3) photosynthesis. We also reconstruct the phylogeny of Aristidoideae, comprising Aristida, Sartidia (C(3)), and Stipagrostis (C(4)), using a sample of 11 species, including A. longifolia, and DNA sequences of the nuclear ribosomal internal transcribed spacer region and the chloroplast rpl16 intron and trnL-trnF region. Sartidia and Stipagrostis resolve as sisters, and sister to this clade is Aristida. Aristida longifolia resolves as sister to the remaining species in the genus. C(3) photosynthesis is hypothesized to be ancestral in Aristidoideae, which means the C(4) pathway evolved twice in the subfamily-in Stipagrostis and early in the diversification of the Aristida clade.     

Woody tissue photosynthesis and its contribution to trunk growth and bud development in young plants

Stem photosynthesis can contribute significantly to woody plant carbon balance, particularly in times when leaves are absent or in ‘open’ crowns with sufficient light penetration. We explored the significance of woody tissue (stem) photosynthesis for the carbon income in three California native plant species via measurements of chlorophyll concentrations, radial stem growth, bud biomass and stable carbon isotope composition of sugars in different plant organs. Young plants of Prunus ilicifolia, Umbellularia californica and Arctostaphylos manzanita were measured and subjected to manipulations at two levels: trunk light exclusion (100 and 50%) and complete defoliation. We found that long‐term light exclusion resulted in a reduction in chlorophyll concentration and radial growth, demonstrating that trunk assimilates contributed to trunk carbon income. In addition, bud biomass was lower in covered plants compared to uncovered plants. Excluding 100% of the ambient light from trunks on defoliated plants led to an enrichment in ¹³C of trunk phloem sugars. We attributed this effect to a reduction in photosynthetic carbon isotope discrimination against ¹³C that in turn resulted in an enrichment in ¹³C of bud sugars. Taken together our results reveal that stem photosynthesis contributes to the total carbon income of all species including the buds in defoliated plants.     

聚四氟乙烯塑料管研磨法对测定C4植物碳同位素比值的影响

聚四氟乙烯(PTFE)塑料管研磨法是测定植物碳同位素比率(δ¹³C)值常用的前处理方法。该方法处理样品高效快捷,但对植物δ¹³C可能存在污染。本研究利用人工气候室开展双因素交互试验,包括空气相对湿度(50%和80%)和空气δ¹³C(¹³C富集和贫化的空气)两个因素,对比了PTFE塑料管研磨法和不锈钢管研磨法处理C4植物糙隐子草δ¹³C的结果。结果表明: 在相同湿度条件下,不同空气δ¹³C处理的植物¹³C分馏值(Δ¹³C,矫正了光合作用底物的δ¹³C差异)原本可以视为重复,但由于PTFE塑料颗粒的混入,相同湿度不同¹³C丰度空气培养下植物叶片Δ¹³C平均差值为4.8‰。该污染效应导致单个叶片δ¹³C测定的误差高达8‰。考虑到C4植物的Δ¹³C较低(通常为1‰~8‰),这种污染效应已经超出了可以接受的误差范围。通过建立类似Keeling曲线的二元混合模型对误差进行了有效消除,并准确估算了植物样品和污染物的δ¹³C。说明广泛采用的PTFE管研磨方法对研究C4植物Δ¹³C并不适用,将导致较大的误差。对精度要求较高的研究内容建议使用不锈钢瓶进行研磨。     

C<Subscript>4</Subscript> plants in the deserts of China: occurrence of C<Subscript>4</Subscript> photosynthesis and its morphological functional types

C₄ photosynthetic pathway and morphological functional types were determined for 104 species in 45 genera and 10 families from the deserts of China. 67 C₄ species (64.4 %) were found in Dicotyledoneae (e.g. Chenopodiaceae, Polygonaceae, and Amaranthaceae), the other 37 species were in Monocotyledoneae (e.g. Gramineae, Cyperaceae, and Commelinaceae). 36.5 % of the Chenopodiaceae species (predominantly members of the genera Anabasis, Atriplex, Kochia, Salsola, and Suaeda) identified in the desert regions were found with C₄ photosynthesis, which was about 48 % of the total C₄ species. Many C₄ species (58.7 %) were annuals (e.g. Amaranthus, Atriplex, Digitaria, Eragrostis, Kochia, and Salsola) and experienced long-term droughts, high temperature, and high irradiance. Relatively more shrub C₄ species (28 species of 104) were found in Chenopodiaceae (e.g. Anabasis, Camphorosma, Haloxylon, and Salsola) and Polygonaceae (e.g. Calligonum) in the desert regions. Most of shrub C₄ species with small leaf area were no more than 1 m in height and distributed in sandy soils. Composition of relatively more annual species, shrubs, and Chenopodiaceae C₄ species was the primary characteristic for the C₄ species occurrence in deserts, and this was remarkably related with the arid environmental conditions.     

C4 photosynthesis: discovery and resolution

This Minireview provides a brief account of the scene and interesting turn of events surrounding the discovery and resolution of the mechanism of C₄ photosynthesis, as well as the recognition of the process by the wider plant science community. This revised version was published online in June 2006 with corrections to the Cover Date.     

Contributions of C3 and C4 plants to higher trophic levels in an Amazonian savanna

We studied the energy flow from C₃ and C₄ plants to higher trophic levels in a central Amazonian savanna by comparing the carbon stable-isotope ratios of potential food plants to the isotope ratios of species of different consumer groups. All C₄ plants encountered in our study area were grasses and all C₃ plants were bushes, shrubs or vines. Differences in δ¹³C ratios among bushes (xˉ = −30.8, SD = 1.2), vines (xˉ = −30.7, SD = 0.46) and trees (xˉ = −29.7, SD = 1.5) were small. However the mean δ¹³C ratio of dicotyledonous plants (xˉ = −30.4, SD = 1.3) was much more negative than that of the most common grasses (xˉ = −13.4, SD = 0.27). The insect primary consumers had δ¹³C ratios which ranged from a mean of −29.5 (SD = 0.47) for the grasshopper Tropidacris collaris to a mean of −14.7 (SD = 0.56) for a termite (Nasutitermes sp.), a range similar to that of the vegetation. However, the common insectivorous and omnivorous vertebrates had intermediate values for δ¹³C, indicating that carbon from different autotrophic sources mixes rapidly as it moves up the food chain. Despite this mixing, the frogs and lizards generally had higher values of δ¹³C (xˉ = −21.7, SD = 1.6; xˉ = −21.9, SD = 1.8, respectively) than the birds (xˉ = −24.8, SD = 1.8) and the only species of mammal resident in the savanna (xˉ = −25.4), indicating that they are generally more dependent on, or more able to utilise, food chains based on C₄ grasses. Received: 7 May 1998 / Accepted: 30 November 1998     

Acclimation of photosynthesis to temperature in eight cool and warm climate herbaceous C3 species: Temperature dependence of parameters of a biochemical photosynthesis model

To determine how parameters of a Farquhar-type photosynthesis model varied with measurement temperature and with growth temperature, eight cool and warm climate herbaceous crop and weed species were grown at 15 and 25 °C and single leaf carbon dioxide and water vapor exchange rates were measured over the range of 15 – 35 °C. Photosynthetic parameters examined were the initial slope of the response of assimilation rate (A) to substomatal carbon dioxide concentration (C_i), A at high C_i, and stomatal conductance. The first two measurements allow calculation of V_Cmax, the maximum rate of carboxylation of ribulose bisphosphate carboxylase and J_max, the maximum rate of photosynthetic electron transport, of Farquhar-type photosynthesis models. In all species, stomatal conductance increased exponentially with temperature over the whole range of 15 – 35 °C, even when A decreased at high measurement temperature. There were larger increases in conductance over this temperature range in the warm climate species (4.3 ×) than in the cool climate species (2.5 ×). The initial slope of A vs. C_i exhibited an optimum temperature which ranged from 20 to 30 °C. There was a larger increase in the optimum temperature of the initial slope at the warmer growth temperature in the cool climate species than in the warm climate species. The optimum temperature for A at high C_i ranged from 25 to 30 °C among species, but changed little with growth temperature. The absolute values of both the initial slope of A vs. C_i and A at high C_i were increased about 10% by growth at the warmer temperature in the warm climate species, and decreased about 20% in the cool climate species. The ratio of J_max — V_Cmax normalized to 20 °C varied by more than a factor of 2 across species and growth temperatures, but differences in the temperature response of photosynthesis were more related to variation in the temperature dependencies of J_max and V_Cmax than to the ratio of their normalized values.This revised version was published online in October 2005 with corrections to the Cover Date.     

Examining the response of needle carbohydrates from Siberian larch trees to climate using compound‐specific δ13C and concentration analyses

Little is known about the dynamics of concentrations and carbon isotope ratios of individual carbohydrates in leaves in response to climatic and physiological factors. Improved knowledge of the isotopic ratio in sugars will enhance our understanding of the tree ring isotope ratio and will help to decipher environmental conditions in retrospect more reliably. Carbohydrate samples from larch (Larix gmelinii) needles of two sites in the continuous permafrost zone of Siberia with differing growth conditions were analysed with the Compound‐Specific Isotope Analysis (CSIA). We compared concentrations and carbon isotope values (δ¹³C) of sucrose, fructose, glucose and pinitol combined with phenological data. The results for the variability of the needle carbohydrates show high dynamics with distinct seasonal characteristics between and within the studied years with a clear link to the climatic conditions, particularly vapour pressure deficit. Compound‐specific differences in δ¹³C values as a response to climate were detected. The δ¹³C of pinitol, which contributes up to 50% of total soluble carbohydrates, was almost invariant during the whole growing season. Our study provides the first in‐depth characterization of compound‐specific needle carbohydrate isotope variability, identifies involved mechanisms and shows the potential of such results for linking tree physiological responses to different climatic conditions.     

Biochar amendment boosts photosynthesis and biomass in C3 but not C4 plants: A global synthesis

Biochar is a carbon (C)‐rich solid produced from the thermochemical pyrolysis of biomass. Its amendment to soils has been proposed as a promising mean to mitigate greenhouse gas emissions and simultaneously benefit agricultural crops. However, how biochar amendment affects plant photosynthesis and growth remains unclear, especially on a global scale. In this study, we conducted a global synthesis of 74 publications with 347 paired comparisons to acquire an overall tendency of plant photosynthesis and growth following biochar amendment. Overall, we found that biochar amendment significantly increased photosynthetic rate by 27.1%, and improved stomatal conductance, transpiration rate, water use efficiency, and chlorophyll concentration by 19.6%, 26.9%, 26.8%, and 16.1%, respectively. Meanwhile, plant total biomass, shoot biomass, and root biomass increased by 25.4%, 22.1%, and 34.4%, respectively. Interestingly, plant types (C₃ and C₄ plants) showed greater control over plant photosynthesis and biomass than a broad suite of soil and biochar factors. Biochar amendment largely boosted photosynthesis and biomass on C₃ plants, but had a limited effect on C₄ plants. Our results highlight the importance of the differential response of plant types to biochar amendment with respect to plant growth and photosynthesis, providing a scientific foundation for making reasonable strategies towards an extensive application of biochar for agricultural production management.     

The efficiency of C4 photosynthesis under low light conditions in Zea mays,Miscanthus x giganteus and Flaveria bidentis

The efficiency of C₄ photosynthesis in Zea mays, Miscanthus x giganteus and Flaveria bidentis in response to light was determined using measurements of gas exchange, ¹³CO₂ photosynthetic discrimination, metabolite pools and spectroscopic assays, with models of C₄ photosynthesis and leaf ¹³CO₂ discrimination. Spectroscopic and metabolite assays suggested constant energy partitioning between the C₄ and C₃ cycles across photosynthetically active radiation (PAR). Leakiness (φ), modelled using C₄ light‐limited photosynthesis equations (φ_mod), matched values from the isotope method without simplifications (φ_is) and increased slightly from high to low PAR in all species. However, simplifications of bundle‐sheath [CO₂] and respiratory fractionation lead to large overestimations of φ at low PAR with the isotope method. These species used different strategies to maintain similar φ. For example, Z. mays had large rates of the C₄ cycle and low bundle‐sheath cells CO₂ conductance (g_bs). While F. bidentis had larger g_bs but lower respiration rates and M. giganteus had less C₄ cycle capacity but low g_bs, which resulted in similar φ. This demonstrates that low g_bs is important for efficient C₄ photosynthesis but it is not the only factor determining φ. Additionally, these C₄ species are able to optimize photosynthesis and minimize φ over a range of PARs, including low light.     

Photosynthetic characteristics and tolerance to photo-oxidation of transgenic rice expressing C4 photosynthesis enzymes

The photosynthetic characteristics of four transgenic rice lines over-expressing rice NADP-malic enzyme (ME), and maize phosphoenolpyruvate carboxylase (PC), pyruvate,orthophosphate dikinase (PK), and PC+PK (CK) were investigated using outdoor-grown plants. Relative to untransformed wild-type (WT) rice, PC transgenic rice exhibited high PC activity (25-fold increase) and enhanced activity of carbonic anhydrase (more than two-fold increase), while the activity of ribulose-bisphosphate carboxylase/oxygenase (Rubisco) and its kinetic property were not significantly altered. The PC transgenic plants also showed a higher light intensity for saturation of photosynthesis, higher photosynthetic CO₂ uptake rate and carboxylation efficiency, and slightly reduced CO₂ compensation point. In addition, chlorophyll a fluorescence analysis indicates that PC transgenic plants are more tolerant to photo-oxidative stress, due to a higher capacity to quench excess light energy via photochemical and non-photochemical means. Furthermore, PC and CK transgenic rice produced 22–24% more grains than WT plants. Taken together, these results suggest that expression of maize C₄ photosynthesis enzymes in rice, a C₃ plant, can improve its photosynthetic capacity with enhanced tolerance to photo-oxidation. This revised version was published online in June 2006 with corrections to the Cover Date.     

Four sites with contrasting environmental stress in southeastern Brazil: relations of species, life form diversity, and geographic distribution to ecophysiological parameters

Some ecophysiological parameters related to plant performance and fitness (carbon and nitrogen isotope composition and total C and N concentrations; in situ chlorophyll fluorescence measurements) were determined for over 30 species in four habitats bordering the montane Atlantic rain forest of Brazil, along a gradient of altitude and rainfall: a dry coastal forest, two areas of sandy coastal plain vegetation (restingas) , and a high altitude campo. There was a considerable diversity of ecophysiological behaviour within and between the functional groups we created based on plant life-forms. For instance, both crassulacean acid metabolism (CAM) and C₃ species were found in most life-forms sampled and throughout all habitats. Despite the variation in rainfall regimes, average overall water-use efficiency was similar between sites, particularly for C₃ species, while no clear pattern regarding nitrogen-use emerged in this respect. Acute and chronic photoinhibition were found in many species across this gradient, even in CAM plants. However, on average, chronic photoinhibition and lower energy dissipation capacity were more characteristic of plants from the restinga habitats. This suggests that, although plants colonizing these habitats have evolved features to deal with water shortage, adaptation to high light levels has not been fully achieved yet. The ecophysiological performance of some individual species in distinct habitats and in distinct microhabitats within habitats is also discussed.     

Models of carbon metabolism in C3-C4 intermediate plants as applied to the evolution of C4 photosynthesis

Abstract Models developed to explain the biphasic response of CO₂ compensation concentration to O₂ concentration and the C₃-like carbon isotope discrimination in C₃-C₄ intermediate species are used to characterize quantitatively the steps necessary in the evolution of C₄ photosynthesis. The evolutionary stages are indicated by model outputs, CO₂ compensation concentration and δ₁₃C value. The transition from intermediate plants to C₄ plants requires the complete formation of C₄ cycle capacity, expressed by the models as transition from C₄ cycle limitation by phosphoenolpyruvate (PEP) regeneration rate to limitation by PEP carboxylase activity. Other steps refer to CO₂ leakage from bundle sheath cells, to further augmentations of C₄ cycle components, to the repression of ribulose-1,5-bisphos-phate carboxylase in the mesophyll cells, and to a decrease in the CO₂ affinity of the enzyme. Possibilities of extending the suggested approach to other physiological characteristics, and the adaptive significance of the steps envisaged, are discussed.