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Biogenic NO emissions from soils (SNOx) play important direct and indirect roles in tropospheric chemistry. The most widely applied algorithm to calculate SNOx in global models was published 15 years ago by Yienger and Levy (1995), and was based on very few measurements. Since then, numerous new measurements have been published, which we used to build up a compilation of world wide field measurements covering the period from 1978 to 2010. Recently, several satellite-based top-down approaches, which recalculated the different sources of NOx (fossil fuel, biomass burning, soil and lightning), have shown an underestimation of SNOx by the algorithm of Yienger and Levy (1995). Nevertheless, to our knowledge no general improvements of this algorithm, besides suggested scalings of the total source magnitude, have yet been published. Here we present major improvements to the algorithm, which should help to optimize the representation of SNOx in atmospheric-chemistry global climate models, without modifying the underlying principals or mathematical equations. The changes include: (1) using a new landcover map, with twice the number of landcover classes, and using annually varying fertilizer application rates; (2) adopting a fraction of 1.0 % for the applied fertilizer lost as NO, based on our compilation of measurements; (3) using the volumetric soil moisture to distinguish between the wet and dry states; and (4) adjusting the emission factors to reproduce the measured emissions in our compilation (based on either their geometric or arithmetic mean values). These steps lead to increased global annual SNOx, and our total above canopy SNOx source of 8.6 Tg yr−1 (using the geometric mean) ends up being close to one of the satellite-based top-down approaches (8.9 Tg yr−1). The above canopy SNOx source using the arithmetic mean is 27.6 Tg yr−1, which is higher than all previous estimates, but compares better with a regional top-down study in eastern China. This suggests that both top-down and bottom-up approaches will be needed in future attempts to provide a better calculation of SNOx.
Which factors determine whether a stimulus is consciously perceived or unconsciously processed? Here, I investigate how previous experience on two different time scales – long term experience over the course of several days, and short term experience based on the previous trial – impact conscious perception. Regarding long term experience, I investigate how perceptual learning does not only change the capacity to process stimuli, but also the capacity to consciously perceive them. To this end, subjects are trained extensively to discriminate between masked stimuli, and concurrently rate their subjective experience. Both the ability to discriminate the stimuli as well as subjective awareness of the stimuli increase as a function of training. However, these two effects are not simple byproducts of each other. On the contrary, they display different time courses, with above chance discrimination performance emerging before subjective experience; importantly, the two learning effects also rely on different circuits in the brain: Moving the stimuli outside the trained receptive field size abolishes the learning effects on discrimination ability, but preserves the learning effects on subjective awareness.
This indicates that the receptive fields serving subjective experience are larger than the ones serving objective performance, and that the channels through which they receive their information are arranged in parallel. Regarding short term experience, I investigate how memory based predictions arising from information acquired on the trial before affect visibility and the neural correlates of consciousness. To this end, I vary stimulus evidence as well as predictability and acquire electroencephalographic data.
A comparison of the neural processes distinguishing consciously perceived from unperceived trials with and without predictions reveals that predictions speed up processing, thus shifting the neural correlates forward in time. Thus, the neural correlates of consciousness display a previously unappreciated flexibility in time and do not arise invariably late as had been predicted by some theorists.
Admittedly, however, previous experience does not always stabilize perception. Instead, previous experience can have the reverse effect: Seeing the opposite of what was there, as in so-called repulsive aftereffects. Here, I investigate what determines the direction of previous experience using multistable stimuli. In a functional magnetic resonance imaging experiment, I find that a widespread network of frontal, parietal, and ventral occipital brain areas is involved in perceptual stabilization, whereas the reverse effect is only evident in extrastriate cortex. This areal separation possibly endows the brain with the flexibility to switch between exploiting already available information and emphasizing the new.
Taken together, my data show that conscious perception and its neuronal correlates display a remarkable degree of flexibility and plasticity, which should be taken into account in future theories of consciousness.
Residual circulation trajectories and transit times into the extratropical lowermost stratosphere
(2011)
Transport into the extratropical lowermost stratosphere (LMS) can be divided into a slow part (time-scale of several months to years) associated with the global-scale stratospheric residual circulation and a fast part (time-scale of days to a few months) associated with (mostly quasi-horizontal) mixing (i.e. two-way irreversible transport, including extratropical stratosphere-troposphere exchange). The stratospheric residual circulation may be considered to consist of two branches: a deep branch more strongly associated with planetary waves breaking in the middle to upper stratosphere, and a shallow branch associated with synoptic and planetary scale waves breaking in the subtropical lower stratosphere. In this study the contribution due to the stratospheric residual circulation alone to transport into the LMS is quantified using residual circulation trajectories, i.e. trajectories driven by the (time-dependent) residual mean meridional and vertical velocities. This contribution represents the advective part of the overall transport into the LMS and can be viewed as providing a background onto which the effect of mixing has to be added. Residual mean velocities are obtained from a comprehensive chemistry-climate model as well as from reanalysis data. Transit times of air traveling from the tropical tropopause to the LMS along the residual circulation streamfunction are evaluated and compared to recent mean age of air estimates. A time-scale separation with much smaller transit times into the mid-latitudinal LMS than into polar LMS is found that is indicative of a separation of the shallow from the deep branch of the residual circulation. This separation between the shallow and the deep circulation branch is further manifested in a distinction in the aspect ratio of the vertical to meridional extent of the trajectories, the integrated mass flux along the residual circulation trajectories, as well as the stratospheric entry latitude of the trajectories. The residual transit time distribution reproduces qualitatively the observed seasonal cycle of youngest air in the extratropical LMS in fall and oldest air in spring.
A complete, well-preserved record of the Cenomanian/Turonian (C/T) Oceanic Anoxic Event 2 (OAE-2) was recovered from Demerara Rise in the southern North Atlantic Ocean (ODP site 1260). Across this interval, we determined changes in the stable carbon isotopic composition of sulfur-bound phytane (δ13Cphytane, a biomarker for photosynthetic algae. The δ13Cphytane record shows a positive excursion at the onset of the OAE-2 interval, with an unusually large amplitude (~7 ‰) compared to existing C/T proto-North Atlantic δ13Cphytane records (3–6 ‰). Overall, the amplitude of the excursion of δ13Cphytane decreases with latitude. Using reconstructed sea surface temperature (SST) gradients for the proto-North Atlantic, we investigated environmental factors influencing the latitudinal δ13Cphytane gradient. The observed gradient is best explained by high productivity at DSDP Site 367 and Tarfaya basin before OAE-2, which changed in overall high productivity throughout the proto-North Atlantic during OAE-2. During OAE-2, productivity at site 1260 and 603B was thus more comparable to the mid-latitude sites. Using these constraints as well as the SST and δ13Cphytane-records from Site 1260, we subsequently reconstructed pCO2 levels across the OAE-2 interval. Accordingly, pCO2 decreased from ca. 1750 to 900 ppm during OAE-2, consistent with enhanced organic matter burial resulting in lowering pCO2. Whereas the onset of OAE-2 coincided with increased pCO2, in line with a volcanic trigger for this event, the observed cooling within OAE-2 probably resulted from CO2 sequestration in black shales outcompeting CO2 input into the atmosphere. Together these results show that the ice-free Cretaceous world was sensitive to changes in pCO2 related to perturbations of the global carbon cycle.
A second genus and species of Nearctic keroplatid fungus gnats (Diptera: Sciaroidea: Keroplatidae: Macrocerinae) attributed to the tribe Robsonomyiini is described: Calusamyia hribari Coher, n. gen., n. sp.. The relationship of this fly from the Florida Keys with Asian genera and species and the single Nearctic described form of the robsonomyiines is briefly discussed.
The Mesoamerican species of Telephanus distinguished by the presence eight lateral pronotal spines
and long temples are reviewed. The group includes T. serratus Nevermann and two previously undescribed species
that are described herein: T. bellus Thomas, new species, from Costa Rica, and the flightless T. monstrosus
Thomas, new species, from Mexico.
The taxonomically neglected milliped order Glomeridesmida and family Glomeridesmidae (infraclass
Pentazonia, superorder Limacomorpha) inhabit 21, rather than seven, regions of the world, being newly recorded
from Thailand; Cambodia; the Republics of Palau, the Philippines, and Vanuatu; New Britain, Bismarck Archipelago;
the Island of New Guinea (both West Papua [formerly Irian Jaya], Indonesia, and Papua New Guinea);
and Sulawesi and Borneo, Indonesia. Occurrence in Fiji is confirmed with two additional samples, and discovery is
predicted in southern China, Myanmar, and perhaps Madagascar. Coupled with published localities, these records
suggest subcontinuous (super)ordinal and familial ranges extending some 12,480 km (7,800 mi) southeastward from
northwestern Thailand to Fiji. Though infrequently encountered, the taxa may actually be diverse and abundant
within this area, which encompasses all of the Indochina and Malay peninsulas, the Philippines, Palau, the Island
of Borneo and Indonesia, Papua New Guinea, the Solomon and Santa Cruz Islands, Vanuatu, and Fiji; it excludes
Taiwan, Australia, New Caledonia, and the Loyalty Islands. The paucity of preserved individuals probably results
from their dark pigmentations and minute sizes, adults being <6.5 mm long; Berlese extractions and sieved litter
techniques are recommended over hand collecting. Glomeridesmida are much more continuous, widespread, and
abundant in the “east” than previously believed and clearly do not comprise a minor, insignificant taxon. The first
glomeridesmidan photos are published.
The southern Appalachian millipeds Boraria stricta (Brölemann, 1896) and B. infesta (Chamberlin, 1918) (Diplopoda: Polydesmida: Xystodesmidae) have become established in Westchester Co., New York, and Hartford Co., Connecticut, respectively. Only three individuals are available for the latter, but B. stricta has established a reproducing population in southern New York state. This species is also recorded from Bland Co., Virginia, in the Ridge and Valley Physiographic Province. Boraria profuga (Causey, 1955) comprises two allopatric populations, one in Montgomery Co., Arkansas, and the other in Ouachita Parish, Louisiana. Distributional records and gonopod drawings are presented for these species plus B. deturkiana (Causey, 1942).
Of the 9 known species of Phylocentropus Banks (Trichoptera: Dipseudopsidae), 5 are found in
eastern North America, 1 in Japan, and 3 in Southeast Asia. Three new species of this genus: Ph. tohoku, Ph.
ngoclinh, and Ph. anas from Vietnam are described and illustrated herein. Previously, only 1 species, Ph.
vietnamellus Mey 1995, was known from this country.
Monneoncideres, a new genus of Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) is described and illustrated. Six new species of Onciderini are also described and illustrated: Hesycha tavakiliani from Brazil; Lesbates milleri from Venezuela; Monneoncideres cristata from Ecuador and Peru; Neodillonia waltersi from Ecuador; Tibiosioma martinsi from Ecuador; and Trestonia wappesi from Panama. Keys to the known species of Lesbates Dillon and Dillon, 1945 and Tibiosioma Martins and Galilleo, 1990 are provided. The genus Ophthalmocydrus Aurivillius, 1925 (Onciderini) is transferred to Pteropliini (Lamiinae); and Xylomimus Bates, 1865 (Apomecynini) is transferred to Onciderini. The following new synonymies are proposed: Kuauna Martins and Galileo, 2009 = Opthalmocydrus Aurivillius, 1925; Kuauna schmidi Martins and Galileo, 2009 = Ophthalmocydrus semiorbifer Aurivillius, 1925; Paraplerodia Martins and Galileo, 2010 = Tibiosioma Martins and Galileo, 2007; Paraplerodia acarinata Martins and Galileo, 2010 = Tibiosioma maculosa Martins and Galileo, 2007; and Ischiomaeocles Franz, 1954 = Lochmaeocles Bates, 1880. The following new combination is proposed: Lochmaeocles salvadorensis (Franz, 1954), transferred from Ischiomaeocles. The following 37 new country records are reported: Alexera barii (Jekel, 1861) (Bolivia, Ecuador); Bacuris sexvittatus (Bates, 1865) (Panama); Cacostola brasiliensis Thomson, 1868 (Argentina); Cherentes niveilateris (Thomson, 1868) (French Guiana); Cicatrodea monima Dillon and Dillon, 1946 (Ecuador); Clavidesmus metallicus (Thomson, 1868) (Ecuador, Peru); Cydros leucurus Pascoe, 1866 (Brazil); Ecthoea quadricornis (Olivier, 1792) (Ecuador); Eudesmus grisescens Audinet-Serville, 1835 (Ecuador, Trinidad and Tobago, Venezuela); Euthima variegata (Aurivillius, 1921) (Ecuador); Hesychotypa heraldica (Bates, 1872) (Belize, Guatemala); Hesychotypa punctata Martins, 1979 (Peru); Lochmaeocles basalis Dillon and Dillon, 1946 (Ecuador, Trinidad and Tobago); Lochmaeocles zonatus Dillon and Dillon, 1946 (Venezuela); Lydipta conspersa (Aurivillius, 1922) (Peru); Neocherentes dilloniorum Tippmann, 1960 (Brazil); Neolampedusa obliquator (Fabricius, 1801) (Ecuador); Peritrox perbra Dillon and Dillon, 1945 (Ecuador); Priscatoides tatila Dillon and Dillon, 1945 (Bolivia); Strioderes peruanus Giorgi, 2001 (Brazil); Trachysomus apipunga Martins and Galileo, 2008 (Peru); Trachysomus camelus Buquet, 1852 (Venezuela); Trachysomus peregrinus Thomson, 1858 (Ecuador); Trachysomus thomsoni Aurivillius, 1923 (Venezuela); Trestoncideres laterialba Martins and Galileo, 1990 (Brazil); Trestonia exotica Galileo and Martins, 1990 (Ecuador); Trestonia fulgurata Buquet, 1859 (Grenada, Trinidad and Tobago); Tritania dilloni Chalumeau, 1990 (Venezuela); Tulcus paganus (Pascoe, 1859) (Ecuador); Xylomimus baculus Bates, 1865 (French Guiana). Theobroma cacao Linnaeus (Sterculiaceae) is recorded as a new host plant record for Eudesmus grisescens.
The taxonomy of the African and Madagascan species of the tiger beetle genus Chaetodera Jeannel 1946 (Coleoptera: Cicindelidae) is reviewed based on studies of primary types and additional museum specimens. Six species are recognized: C. andriana (Alluaud 1900), C. antatsima (Alluaud 1902), C. blanchardi (Fairmaire 1882), C. maheva (Künckel d’Herculais 1887), C. perrieri (Fairmaire 1897), and C. regalis (Dejean 1831). All species are illustrated, including color variants, and a key to species and maps of species distributions are provided. A hypothesis of phylogenetic relationships is proposed for the nine worldwide species of the genus Chaetodera based on computerized parsimony analysis of a matrix containing data on 16 adult morphological characteristics.
Cephaloleia consanguinea Baly, Cephaloleia fulvolimbata Baly, Cephaloleia ruficollis Baly, Chalepus amabilis Baly, Chalepus brevicornis (Baly), Chalepus pici Descarpentries and Villiers, Microrhopala erebus (Newman), Octhispa bimaculata Uhmann, Octotoma championi Baly, Pseudispa tuberculata Staines, Sceloenopla erudita (Baly), Stenispa guatemalensis Uhmann, Sumitrosis gestroi (Weise), and Sumitrosis terminatus (Baly) (Coleoptera: Chrysomelidae: Cassidinae) are new country records of hispine chrysomelids for Belize, based on collections cited herein. These collections also document new host records for Calyptocephala gerstaeckeri Boheman (Chamaedorea tepejilote Liebm., Arecaceae), Cephaloleia consanguinea (Heliconia bourgaeana Petersen, H. collinsiana Griggs, H. latispatha Benth., H. wagneriana Petersen; Heliconiaceae), and Cephaloleia perplexa Baly (Heliconia bourgaeana, H. latispatha; Heliconiaceae).
Bioapatite in mammalian teeth is readily preserved in continental sediments and represents a very important archive for reconstructions of environment and climate evolution. This project intends to provide a detailed data base of major, minor and trace element and isotope tracers for tooth apatite using a variety of microanalytical techniques. The aim is to identify specific sedimentary environments and to improve our understanding on the interaction between internal metabolic processes during tooth formation and external nutritional control and secondary alteration effects. Here, we use the electron microprobe, to determine the major and minor element contents of fossil and modern molar enamel, cement and dentin from hippopotamids. Most of the studied specimens are from different ecosystems in Eastern Africa, representing modern and fossil lakustrine (Lake Kikorongo, Lake Albert, and Lake Malawi) and modern fluvial environments of the Nile River system.
Secondary alteration effects in particular FeO, MnO, SO3 and F concentrations, which are 2 to 10 times higher in fossil than in modern enamel; secondary enrichments in fossil dentin and cement are even higher. In modern and fossil enamel, along sections perpendicular to the enamel-dentin junction (EDJ) or along cervix-apex profiles, P2O5 and CaO contents and the CaO/P2O5 ratios are very constant (StdDev ~1 %). Linear regression analysis reveals very tight control of the MgO (R2∼0.6), Na2O and Cl variation (for both R2>0.84) along EDJ-outer enamel rim profiles, despite large concentration variations (40 % to 300 %) across the enamel. These minor elements show well defined distribution patterns in enamel, similar in all specimens regardless of their age and origin, as the concentration of MgO and Na2O decrease from the enamel-dentin junction (EDJ) towards the outer rim, whereas Cl displays the opposite variation.
Fossil enamel from hippopotamids which lived in the saline Lake Kikorongo have a much higher MgO/Na2O ratio (∼1.11) than those from the Neogene fossils of Lake Albert (MgO/Na2O∼0.4), which was a large fresh water lake like those in the western Branch of the East African Rift System today. Similarly, the MgO/Na2O ratio in modern enamel from the White Nile River (∼0.36), which has a Precambrian catchment of dominantly granite and gneisses and passes through several saline zones, is higher than that from the Blue Nile River, whose catchment is the Neogene volcanic Ethiopian Highland (MgO/Na2O∼0.22). Thus, particularly MgO/Na2O might be a sensitive fingerprint for environments where river and lake water have suffered strong evaporation.
Enamel formation in mammals takes place at successive mineralization fronts within a confined chamber where ion and molecule transport is controlled by the surrounding enamel organ. During the secretion and maturation phases the epithelium generates different fluid composition, which in principle, should determine the final composition of enamel apatite. This is supported by co-linear relationships between MgO, Cl and Na2O which can be interpreted as binary mixing lines. However, if maturation starts after secretion is completed the observed element distribution can only be explained by recrystallization of existing and addition of new apatite during maturation. Perhaps the initial enamel crystallites precipitating during secretion and the newly formed bioapatite crystals during maturation equilibrate with a continuously evolving fluid. During crystallization of bioapatite the enamel fluid becomes continuously depleted in MgO and Na2O, but enriched in Cl which results in the formation of MgO, and Na2O-rich, but Cl-poor bioapatite near the EDJ and MgO- and Na2O-poor, but Cl-rich bioapatite at the outer enamel rim.
The linkage between lake and river water composition, bioavailability of elements for plants, animal nutrition and tooth formation is complex and multifaceted. The quality and limits of the MgO/Na2O and other proxies have to be established with systematic investigations relating chemical distribution patterns to sedimentary environment and to growth structures developing as secretion and maturation proceed during tooth formation.
Ubiquitin is a highly conserved protein involved in several cellular processes like protein degradation, endocytosis, signal transduction and DNA repair. The discovery of ubiquitin-like proteins (UBL) and ubiquitin-like domains (ULD) increases the number of regulation pathways where the property of the ubiquitin-fold is profitable.
Autophagy is the catabolic pathway used in cells to deliver cytosolic components and dysfunctional organelles to the lysosome for degradation. MAP1LC3 proteins are ubiquitin-like proteins involved in one hand for the expansion of the autophagosome, which sequesters cytosolic substrates. In the other hand, these proteins (LC3- and GABARAP- subfamilies) bind to autophagic receptors linked to polyubiquitinated proteins aggregates. For this project, the 3D structure of the GABARAPL-1/NBR1-LIR complex was determined and confirmed that GABARAPL-1 belongs to the MAP1LC3 proteins family, structurally characterized by an ubiquitin-fold, consisting of a central beta-sheet formed by four beta-strands and two alpha-helices on one side of the beta-sheet, preceded N terminally by two alpha-helices, resulting in the formation of two hydrophobic pockets, hp1 and hp2. The autophagic receptor NBR1 interacts with GABARAPL-1 through the hp1 and hp2 with its LIR motif taking an extended beta conformation upon binding, forming an intermolecular beta-sheet with the second beta-strand of GABARAPL 1. This LC3- interacting region (LIR) consists of an Theta XX Gamma sequence preceded by acidic amino acids, with Theta and Gamma represented by any aromatic and hydrophobic residues, respectively. Interaction studies of the LIR domains of p62, Nix and NBR1 with different members of the MAP1LC3 proteins family indicate that the presence of a tryptophan in the LIR motif increases the binding affinity. Substitution to other aromatic amino acids or increasing the number of negatively charged residues at the N-terminus of the LIR motif, however, has little effect on the binding affinity due to enthalpy-entropy compensation, suggesting that effector proteins can interact with a wide variety of different sequences with similar and moderate binding affinities.
Additionally to be present in proteins dealing with protein folding and degradation, ubiquitin-like domain were found protein involved in the regulation of signal transduction like TBK1, a serine/threonine kinase responsible for induction of immune response. In this second project, based on the NMR chemical shifts of the TBK1 domain contained between amino acids 302 and 383, secondary structure prediction programs (TALOS and CSI) confirmed the presence of an Ubiquitin-like domain in TBK1 by identifying one alpha-helix and four beta-strands sequentially aligned like following beta-beta-alpha-beta-beta. This alignment corresponds perfectly with the secondary structure elements of Ubiquitin and proved that TBK1_ULD belongs to the UBL protein superfamily. The similarity to ubiquitin was even bigger by the presence in addition of a small beta-strand and a short helix, which are observed as the beta 5-strand and a 310-helix in Ubiquitin, respectively. The first attempts on the 3D structure determination confirmed the Ub-fold but due to the lack of assignment in TBK1_ULD, only a structure based on ubiquitin as a model was determined. Interaction studies of TBK1_ULD with the IAD-SRR domain of IRF3 showed that both side of the molecule seems involved and that the TBK1/IRF3 interaction is more complex than a one to one binding process. Unfortunately, the instability of TBK1_ULD associated to the difficulty in the purification of IAD-SRR did not allow to further study this interaction more precisely.
Finally, to overcome the difficulty encountered in NMR experiments because of low expression and/or poor solubility, an expression vector using the intrinsic property of ubiquitin was designed. Fused to proteins or peptides targets, this construct produced proteins and peptides in a larger amount than with traditional expression vectors and also with a less cost than chemical synthesis for pure labeled peptides for NMR structural studies. The presence of a hexa histidine tag was useful for the isolation and the purification of the constructs. The existence of a TEV cleavage site was created to keep the possibility of releasing the ubiquitin moiety from the expressed protein or peptide. Moreover, the ubiquitin-tag could also still be attached to the protein/peptide of interest when biophysical methods like NMR, ITC or CD spectroscopy are applied, providing the same results than for the protein/peptide moiety alone.
The alticine genera Hemiphrynus Horn 1889 and Phrynocepha Baly 1861 (Coleoptera: Chrysomelidae) are reviewed and their status clarified. Both genera and all previously known species are redescribed. Four new species of Hemiphrynus are described: H. barri, H. corrugatus, H. smithi, and H. sydneyae. Six new species of Phrynocepha are described: P. australis, P. kendrae, P. marciae, P. natalieae, P. pseudocapitata, and P. pueblae. The following new combination is proposed: Hemiphrynus elongatus (Jacoby 1884) transferred from Phrynocepha. Hemiphrynus sulcatipennis Jacoby 1891 and H. tenuicornis Jacoby 1891 are reinstated in Hemiphrynus, incertae sedis. Hemiphrynus elongatus is recorded from New Mexico, a new record for the United States. Lectotypes are here designated for the following species: H. elongatus, H. intermedius (Jacoby 1884), H. sulcatipennis, H. tenuicornis, P. capitata Jacoby 1884, P. deyrollei Baly 1876, and P. pulchella Baly 1861. A key to differentiate the two genera and keys to the species in both genera are provided. Host records are given for a few species of both Hemiphrynus and Phrynocepha. Distribution maps are presented for all species.
Agriculture of crops provides more than 85% of the energy in human diet, while also securing income of more than 2.6 billion people. To investigate past, present and future changes in the domain of food security, water resources and water use, nutrient cycles, and land management it is required to know the agricultural land use, in particular which crop grows where and when. The current global land use or land cover data sets are based on remote sensing and agricultural census statistics. In general, these only contain one or very few classes of agricultural land use. When crop-specific areas are given, no distinction of irrigated and rainfed areas is made, whereas it is necessary to distinguish rainfed and irrigated crops, because crop productivity and water use differ significantly between them.
To support global-scale assessments that are sensitive to agricultural land use, the global data set of Monthly Irrigated and Rainfed Crop Areas around the year 2000 (MIRCA2000) was developed by the author. With a spatial resolution of 5 arc-minutes (approximately 9.2 km at the equator), MIRCA2000 provides for the first time, spatially explicit irrigated and rainfed crop areas separately for each of the 26 crop classes for each month of the year, and includes multi-cropping. The data set covers all major food crops as well as cotton, while the remaining crops are grouped into three categories (perennial, annual and fodder grasses). Also for the first time, crop calendars on national or sub-national level were consistently linked to annual values of harvested area at the 5 arc-minutes grid cell level, such that monthly growing areas could be computed that are representative for the time period 1998 to 2002.
The downscaling algorithm maximizes the consistency to the grid-based input data of cropland extent [Ramankutty et al., 2008], crop-specific total annual harvested area [Monfreda et al., 2008], and area equipped for irrigation [Siebert et al., 2007]. In addition to the methodology, this dissertation describes differences to other datasets and standard scaling methods, as well as some applications. For quality assessment independent datasets and newly developed quality parameters are used, and scale effects are discussed.
Supplementary Appendices document crop calendars for irrigated and rainfed crops for each of the 402 spatial units (Appendix I), data sources of harvested area and of cropping periods for irrigated crops, country by country (Appendix K), as well as data quality parameters (Appendix L, including spreadsheet files).