Upscaling leaf area index in an Arctic landscape through multiscale observations

Monitoring and understanding global change requires a detailed focus on upscaling, the process for extrapolating from the site‐specific scale to the smallest scale resolved in regional or global models or earth observing systems. Leaf area index (LAI) is one of the most sensitive determinants of plant production and can vary by an order of magnitude over short distances. The landscape distribution of LAI is generally determined by remote sensing of surface reflectance (e.g. normalized difference vegetation index, NDVI) but the mismatch in scales between ground and satellite measurements complicates LAI upscaling. Here, we describe a series of measurements to quantify the spatial distribution of LAI in a sub‐Arctic landscape and then describe the upscaling process and its associated errors. Working from a fine‐scale harvest LAI–NDVI relationship, we collected NDVI data over a 500 m × 500 m catchment in the Swedish Arctic, at resolutions from 0.2 to 9.0 m in a nested sampling design. NDVI scaled linearly, so that NDVI at any scale was a simple average of multiple NDVI measurements taken at finer scales. The LAI–NDVI relationship was scale invariant from 1.5 to 9.0 m resolution. Thus, a single exponential LAI–NDVI relationship was valid at all these scales, with similar prediction errors. Vegetation patches were of a scale of ～0.5 m and at measurement scales coarser than this, there was a sharp drop in LAI variance. Landsat NDVI data for the study catchment correlated significantly, but poorly, with ground‐based measurements. A variety of techniques were used to construct LAI maps, including interpolation by inverse distance weighting, ordinary Kriging, External Drift Kriging using Landsat data, and direct estimation from a Landsat NDVI–LAI calibration. All methods produced similar LAI estimates and overall errors. However, Kriging approaches also generated maps of LAI estimation error based on semivariograms. The spatial variability of this Arctic landscape was such that local measurements assimilated by Kriging approaches had a limited spatial influence. Over scales >50 m, interpolation error was of similar magnitude to the error in the Landsat NDVI calibration. The characterisation of LAI spatial error in this study is a key step towards developing spatio‐temporal data assimilation systems for assessing C cycling in terrestrial ecosystems by combining models with field and remotely sensed data.     

Morphological reinforcement,ancient introgressive hybridization and species delimitation in African stem‐borer species of the genus Sesamia Guenée (Lepidoptera: Noctuidae)

Species delimitation, an issue central to systematics and biodiversity studies, is addressed in the epunctifera group of the stem borer genus Sesamia Guenée (Lepidoptera: Noctuidae). This group is composed of four sub‐Saharan species: Sesamia poephaga Tams & Bowden; Sesamia epunctifera Hampson; Sesamia penniseti Tams & Bowden; and Sesamia poebora Tams & Bowden, the taxonomic status of which was unclear. The first species was considered a possible synonym of the second, and the third species was considered a possible synonym of the fourth. An analysis combining morphological, ecological and molecular data enables us to conclude that S. epunctifera and S. poephaga are different species, and that S. poebora is a synonym of S. penniseti. Two new species were discovered: Sesamia firmata sp.n. and Sesamia veronica sp.n. Sesamia firmata sp.n. has atypical genitalic morphology, suggesting a strong selection resulting in a reinforcement of pre‐zygotic isolation. Some specimens previously identified as S. penniseti on the basis of morphology are sisters to S. epunctifera on the mitochondrial tree, and are connected to S. penniseti on the nuclear tree. The mitochondrial distance from S. penniseti and S. epunctifera is 7.6% and 3.9%, respectively, suggesting an ancient mitochondrial introgression from S. epunctifera into S. penniseti. The possible causes of the reinforcement and introgressive hybridization are discussed. This case of mitochondrial introgression, uncommon in Lepidoptera, in which females are the heterogametic sex, may be an exception to Haldane's rule. The hybrid is assigned the rank of species and named Sesamia pennipuncta sp.n.     

Adverse effects of agricultural intensification and climate change on breeding habitat quality of Black‐tailed Godwits Limosa l. limosa in the Netherlands

Agricultural intensification is one of the main drivers of farmland bird declines, but effects on birds may be confounded with those of climate change. Here we examine the effects of intensification and climate change on a grassland breeding wader, the Black‐tailed Godwit Limosa l. limosa, in the Netherlands. Population decline has been linked to poor chick survival which, in turn, has been linked to available foraging habitat. Foraging habitat of the nidifugous chicks consists of uncut grasslands that provide cover and arthropod prey. Conservation measures such as agri‐environment schemes aim to increase the availability of chick foraging habitat but have not yet been successful in halting the decline. Field observations show that since the early 1980s, farmers advanced their first seasonal mowing or grazing date by 15 days, whereas Godwits did not advance their hatching date. Ringing data indicate that between 1945 and 1975 hatching dates advanced by about 2 weeks in parallel with the advancement of median mowing dates. Surprisingly, temperature sums at median mowing and hatching dates suggest that while the agricultural advancement before 1980 was largely due to agricultural intensification, after 1980 it was largely due to climate change. Examining arthropod abundance in a range of differently managed grasslands revealed that chick food abundance was little affected but that food accessibility in intensively used tall swards may be problematic for chicks. Our results suggest that, compared with 25 years ago, nowadays (1) a much higher proportion of clutches and chicks are exposed to agricultural activities, (2) there is little foraging habitat left when chicks hatch and (3) because of climate change, the vegetation in the remaining foraging habitat is taller and denser and therefore of lower quality. This indicates that for agri‐environment schemes to make a difference, they should not only be implemented in a larger percentage of the breeding area than the current maxima of 20–30% but they should also include measures that create more open, accessible swards.     

The production‐ecological sustainability of cassava,sugarcane and sweet sorghum cultivation for bioethanol in Mozambique

We present an approach for providing quantitative insight into the production‐ecological sustainability of biofuel feedstock production systems. The approach is based on a simple crop‐soil model and was used for assessing feedstock from current and improved production systems of cassava for bioethanol. Assessments were performed for a study area in Mozambique, a country considered promising for biomass production. Our focus is on the potential role of smallholders in the production of feedstock for biofuels. We take cassava as the crop for this purpose and compare it with feedstock production on plantations using sugarcane, sweet sorghum and cassava as benchmarks. Production‐ecological sustainability was defined by seven indicators related to resource‐use efficiency, soil quality, net energy production and greenhouse gas (GHG) emissions. Results indicate that of the assessed systems, sugarcane performed better than cassava, although it requires substantial water for irrigation. Targeted use of nutrient inputs improved sustainability of smallholder cassava. Cassava production systems on more fertile soils were more sustainable than those on less fertile soils; the latter required more external inputs for achieving the same output, affecting most indicators negatively and reducing the feasibility for smallholders. Cassava and sweet sorghum performed similarly. Cassava production requires much more labour per hectare than production of sugarcane or sweet sorghum. Production of bioethanol feedstock on cultivated lands was more sustainable and had potential for carbon sequestration, avoiding GHG emissions from clearing natural vegetation if new land is opened.     

固氮蓝藻高光放氢突变种的筛选和放氢特点

作者以前报道过几种快速生长的固氮蓝藻在某种条件下能好气光放氢,其速度可以达到光合放氧速度的10—15%,但这种活性只有在不积累氢气的流动气相下或在短时间内发生。本文报道用亚硝基胍诱变所得到的Anabaena spp。Strain CA的高光放氢突变种——N9A和18A——的筛选和氢代谢特点。在达生长饱和光照以后,野生型的光放氢活性与光照强度的增加成正相关,而其吸氢活性则与之成负相关,显示高光照强度可能抑制吸氢酶的活性。无论在什么光强下,均测不到两个突变种的吸氢活性,暗示在突变种中,吸氢酶或有关系统受损伤。把细胞固相化在琼脂上,在密闭系统中,高光强下培养50个小时,两个突变种光释放和积累的氢分别为野生型的2倍(N9A)和6倍(18A),后者等于氢占气相(1%CO_2的空气)的1.8%。两个突变种在生长速度、叶绿素含量、乙炔还原活性以及光合放氧方面与野生型无明显不同。当以含50—100nM的镍离子的培养基培养时,野生型的好气净产氢活性完全丢失,其吸氢活性却增加约10倍。培养基中镍离子的存在,对两个突变种的高光放氢活性则毫无影响,而且在此情况下,仍测不出其吸氢活性。实验结果表明,这两个突变种系吸氢酶缺陷型突变种。     

Respiration Rate and Mitochondrial Activity in Iris Bulbs

The oxygen uptake of iris bulbs (Iris×hollandica‘Wedgwood’) which had been stored dry at 30 C (“retarded’ bulbs) was low (10 μmol O₂ per h and bulb), the oxygen uptake of the intact bulb, the three outer fleshy scales and the remaining central part of the bulb increased three- to fourfold, nearly twofold and fourfold, respectively. Mitochondria were isolated from the scales of retarded and activated bulbs and their oxygen consumption with succinate, l -malate (plus pyruvate). x-ketoglutarate and NADH as substrate was measured polarographically. The oxidative capacity of mitochondria isolated from the scales of activated bulbs was only slightly higher than that from retarded bulbs when calculated on a tissue basis. No difference was found between the phosphorylation efficiency, respiratory control, cytochrome c deficiency, succinate dehydrogenase, malate dehydrogenase, succinate-cytochrome c rductase, NADH-cytochrome c reductase and cytochrome oxidase activity of the retarded and activated bulbs. The increase in the in vitro oxygen uptake of the scales after transition from 30 to 13 C was not accompanied by an equal increase in the oxidative capacity of their mitochondria suggesting that they are not responsible for this rise in oxygen uptake.     

CLADISTIC ANALYSIS OF THE SUBORDER CONULARIINA MILLER AND GURLEY, 1896 (CNIDARIA, SCYPHOZOA; VENDIAN–TRIASSIC)

Abstract: Results of a cladistic analysis of the suborder Conulariina Miller and Gurley, 1896, a major extinct (Vendian–Triassic) group of scyphozoan cnidarians, are presented. The analysis sought to test whether the three conulariid subfamilies (Conulariinae Walcott, 1886 , Paraconulariinae Sinclair, 1952 and Ctenoconulariinae Sinclair, 1952 ) recognized in the Treatise on Invertebrate Paleontology (TIP) are monophyletic. A total of 17 morphological characters were scored for 16 ingroup taxa, namely the genera Archaeoconularia, Baccaconularia, Climacoconus, Conularia, Conulariella, Conularina, Ctenoconularia, Eoconularia, Glyptoconularia, Metaconularia, Notoconularia, Paraconularia, Pseudoconularia, Reticulaconularia, Teresconularia and Vendoconularia. The extant medusozoan taxa Cubozoa, Stauromedusae, Coronatae and Semaeostomeae served as outgroups. Unweighted analysisof the data matrix yielded 1057 trees, and successive weighting analysis resulted in one of the 1057 original trees. The ingroup is monophyletic with two autapomorphies: (1) the quadrate geometry of the oral region; and (2) the presence of a mineralized (phosphatic) periderm. Within the ingroup, the clade (Vendoconularia, Teresconularia, Conularina, Eoconularia) is supported by the sinusoidal longitudinal geometry of the transverse ridges, and the much larger clade (Baccaconularia, Glyptoconularia, Metaconularia, Pseudoconularia, Conularia, Ctenoconularia, Archaeoconularia, Notoconularia, Climacoconus, Paraconularia, Reticulaconularia) is supported by the presence of external tubercles, which, however, were lost in the clade (Notoconularia, Climacoconus, Paraconularia, Reticulaconularia). As proposed by Van Iten et al. (2000) , the clade (Notoconularia, Climacoconus, Paraconularia, Reticulaconularia) is supported by the termination and alternation of the transverse ribs in the corner sulcus. The previously recognized subfamilies Conulariinae, Paraconulariinae and Ctenoconulariinae were not recovered from this analysis. The diagnostic features of Conulariinae (continuation of the transverse ornament across the corner sulcus and lack of carinae) and Ctenoconulariinae (presence of carinae) are symplesiomorphic or homoplastic, and Paraconulariinae is polyphyletic. The families Conulariellidae Kiderlen, 1937 and Conulariopsidae Sugiyama, 1942 , also recognized in the TIP, are monogeneric, and since they provide no additional phylogenetic information, should be abandoned.     

Cell Cycle Control in Arabidopsis

Although the basic mechanism of cell cycle control is conservedamong eukaryotes, its regulation differs in each type of organism.Plants have unique developmental features that distinguish themfrom other eukaryotes. These include the absence of cell migration,the formation of organs throughout the entire life-span fromspecialized regions called meristems, and the potency of non-dividingcells to re-enter the cell cycle. The study of plant cell cyclecontrol genes is expected to contribute to the understandingof these unique developmental phenomena. The principal regulatorsof the eukaryotic cell cycle, the cyclin-dependent kinases (CDKs)and cyclins, are conserved in plants. This review focuses oncell cycle regulation in the plant Arabidopsis thaliana . Whileexpression of one Arabidopsis CDK gene, Cdc2aAt, was positivelycorrelated with the competence of cells to divide, expressionof a mitotic-like cyclin, cyc1At, was almost exclusively confinedto dividing cells. The expression of the Arabidopsis -type cyclinsappears to be an early stage in the response of plant cellsto external and internal stimuli. Arabidopsis thaliana (L.) Heynh.; cell cycle; CDK; cyclin; plant development; plant hormone