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Global process-based characterization factors of soil carbon depletion for life cycle impact assessment
<p>The dataset includes all the Life Cycle Impact Assessment (LCIA) Characterization Factors (CFs) for the Soil Organic Carbon (SOC) depletion indicator produced by Teixeira, R.F.M., Morais, T.G., Domingos, T. 2021. Global process-based characterization factors of soil carbon depletion for life cycle impact assessment.</p> <p> </p> <p>The dataset is divided by type of CF. The results (files) included in each file is:</p> <ul> <li><strong>SOC_dynamics.zip</strong>: includes all the used SOC dynamics for calculate the CFs (it includes transitions for crop, forest, grassland and urban LU classes).</li> </ul> <ul> <li><strong>Raster_Background_Occupation.zip</strong>: includes spatial data (rasters at “tif” format) for Occupation CFs per aggregated land use flow according Table 1 of the paper at country-level.</li> </ul> <p>For example, the raster “Occ_background_Agriculture.tif” has the CFs for the land use class “Agriculture”.</p> <ul> <li><strong>Raster_background_Transformation.zip</strong>: includes spatial data (rasters at “tif” format) for Transformation CFs per aggregated land use flow according Table 1 of the paper at country-level.</li> <li><strong>Table_CFs_background.xlsx</strong>: Includes, at Excel table, the Occupation and Transformation Characterization Factors that were included in “Raster_background_ Occupation.zip” and “Raster_background_Transformation.zip”</li> <li><strong>Raster_Foreground_Occupation.zip</strong>: includes spatial data (rasters at “tif” format) for Occupation CFs per unique land use flow according Table 2 of the paper at unique homogenous territorial unit (about 17,200 unique region).</li> </ul> <p>For example, the raster “Occ_foreground_Irrigated_Potatoes.tif” has the CFs for the land use class “Irrigated potatoes”.</p> <ul> <li><strong>Raster_ Foreground _Transformation.zip</strong>: includes spatial data (rasters at “tif” format) for Transformation CFs per unique land use flow according Table 2 of the paper at unique homogenous territorial unit (about 17,200 unique region).</li> <li><strong>Table_CFs_foreground.xlsx: </strong>Includes, at Excel table, the Occupation and Transformation Characterization Factors that were included in “Raster_Foreground_Occupation.zip” and “Raster_ Foreground _Transformation.zip”</li> <li><strong>LCIA_OpenLCA_file.zip</strong>: includes the Background Characterization Factors to be imported as an LCIA methods for the Product Environmental Footprint database in OpenLCA software</li> </ul>
Figure 1 in Life cycles and host-parasitoid relationships of five species of Leucospis wasps in Argentina (Hymenoptera: Leucospidae)
Figure 1. Location of the sampling sites (SC: San Claudio, AN: Anquilóo and MG: Martín García reserve) within the grasslands of Río de la Plata (the area surrounded by a thick line), with satellite images (altitude 5km), and representative photographs of the different vegetation structure at each site (Satellite images copyright Google Inc. 2013).
Figure 2 in Life cycle and behaviour of Charoxus spinifer and Charoxus major (Coleoptera: Staphylinidae: Aleocharinae), predators of fig wasps (Hymenoptera: Agaonidae)
Figure 2. Larva of Charoxus spinifer (instar III) approaching an adult Pegoscapus jimenezi (its prey) in a Ficus aurea syconium. Photograph by Robert Noonan.
Figure 1 in Life cycle and behaviour of Charoxus spinifer and Charoxus major (Coleoptera: Staphylinidae: Aleocharinae), predators of fig wasps (Hymenoptera: Agaonidae)
Figure 1. Left, adult female Charoxus spinifer (Florida, USA). The male (fig. 1 in Frank and Thomas 1997) has a posteriorly projecting prominent spine at each side of abdominal tergite IV, the only reported occurrence of such structures in the genus Charoxus. Right, adult female Charoxus major (Veracruz, Mexico). The male has a relatively longer head and thorax, and longer mouthparts (mandibles and maxillae). Photographs by Lyle Buss, University of Florida.
Figure 6 in Life cycle and population structure of the terrestrial isopod Hemilepistus klugii (Brandt, 1833) (Isopoda: Oniscidea) in Iran
Figure 6. Correlation between cephalothorax width and egg number in ovigerous females of Hemilepistus klugii from Varamin.
Figure 4 in Life cycle and population structure of the terrestrial isopod Hemilepistus klugii (Brandt, 1833) (Isopoda: Oniscidea) in Iran
Figure 4. Frequency distribution of cephalothorax width in Hemilepistus klugii from Varamin from February 2008 to May 2009. Same key as Figure 1.
Figure 3 in Life cycle and population structure of the terrestrial isopod Hemilepistus klugii (Brandt, 1833) (Isopoda: Oniscidea) in Iran
Figure 3. Frequency of ovigerous, post-ovigerous and non-ovigerous females in Hemilepistus klugii during the breeding season (March–April 2008 and 2009) from Varamin based on weekly sampling.
Figure 1 in Life cycle and population structure of the terrestrial isopod Hemilepistus klugii (Brandt, 1833) (Isopoda: Oniscidea) in Iran
Figure 1. Frequency distribution of overall cephalothorax width in Hemilepistus klugii from Varamin.
Figure 1 in Life cycle variation and adaptation in jumping plant lice (Insecta: Hemiptera: Psylloidea): a global synthesis
Figure 1. Dendrogram illustrating the level of correspondence among life history parameters measured across psyllid species. Note: similarity is measured by Euclidean distance; clustering is by average linkage.
FIG. 3. Echinostoma deserticum n in Life cycle of a new African echinostome species reproducing by parthenogenesis
FIG. 3. Echinostoma deserticum n. sp. (A) Cercaria (general morphology); (B) cercaria (lateral view); (C) metacercaria.
FIG. 2. Echinostoma deserticum n in Life cycle of a new African echinostome species reproducing by parthenogenesis
FIG. 2. Echinostoma deserticum n. sp. (A) Miracidium (epidermal cells); (B) miracidium (general morphology); (C) sporocyst; (D) attachment zone of the sporocysts; (E) young daughter redia; (F) mature daughter redia containing cercariae embryos.
Supplementary material 2 from: {"en": "Gavrilov-Zimin IA (2021) Aberrant ontogeneses and life cycles in Paraneoptera. Comparative Cytogenetics 15(3): 253-277. https://doi.org/10.3897/compcytogen.v15.i3.70362"}
Supplementary material 2 from: {"en": "Gavrilov-Zimin IA (2021) Aberrant ontogeneses and life cycles in Paraneoptera. Comparative Cytogenetics 15(3): 253-277. https://doi.org/10.3897/compcytogen.v15.i3.70362"}
Supplementary material 1 from: {"en": "Gavrilov-Zimin IA (2021) Aberrant ontogeneses and life cycles in Paraneoptera. Comparative Cytogenetics 15(3): 253-277. https://doi.org/10.3897/compcytogen.v15.i3.70362"}
Supplementary material 1 from: {"en": "Gavrilov-Zimin IA (2021) Aberrant ontogeneses and life cycles in Paraneoptera. Comparative Cytogenetics 15(3): 253-277. https://doi.org/10.3897/compcytogen.v15.i3.70362"}
FIGURE 4 in Medusoids in the life cycle of Dentitheca dendritica (Nutting, 1900) and Nemalecium gracile sp. nov. (Cnidaria: Hydrozoa)
FIGURE 4. Cnidome of Nemalecium gracile sp. nov. (A–D) and Nemalecium cf. lighti (Hargitt, 1924) from the Caribbean (E–H) and Indonesia (I–L): pseudostenoteles (A, E, I), microbasic mastigophores (B, F, J), microbasic euryteles (C, G, K), and unidentified rhopaloid heteronemes (D, H, L).
FIGURE 3 in Medusoids in the life cycle of Dentitheca dendritica (Nutting, 1900) and Nemalecium gracile sp. nov. (Cnidaria: Hydrozoa)
FIGURE 3. Nemalecium gracile sp. nov.—living colony (A) and hydranth (insert) showing the typical bright yellow tinge of the digestive region and the tentacles raised at different levels; fixed hydranth showing the hypostome (h.) encircled by the row of filiform tentacles (f.t.), the digestive (d.r.) and non-digestive (n.d.r.) regions, as well as ectodermic glandular cells (g.c.); detail of the non-digestive region (C) showing highly vacuolated endodermal cells; detail of a filiform tentacle showing large, endodermal chordal cells (D); insertion of the filiform tentacles (f.t.) around the hypostome, showing conspicuous glandular cells (g.c.) in between; nematodactyl (n.d.) armed with pseudostenoteles (p.s.) and filiform tentacles (f.t.) richly recovered with microbasic mastigophores (m.b.m.) (F); detail of a nematodactyl showing a discharged pseudostenotele (G); female (H) and male (I) gonothecae from dioecious stems; gonotheca and male gonophore, showing the blastostyle (b.) ending in an apical plate (a.p.) and budding off the gonophore, all being covered with a mantle (m.); the slightly eccentric spadix (s.) is distinguished from the mass of sperm cells (s.m.) through its darker tinge (J); male medusoid getting free from its mantle (m.), which remains attached to the blastostyle (b.) (K); newly released male medusoid (L), showing the conspicuous belt of refringent corpuscles (insert); fixed male medusoid seen with transmitted (M) and incident (N) light, showing the velar aperture (left) and the striated subumbrellar ectoderm; detail of the myoepithelial fibers of the subumbrellar ectoderm (O); slightly squashed preparation of a male medusoid showing the spadix (sp.) and a number of pseudostenoteles (p.s.) disseminated among the mass of gametes (P). Scale bars: 30 µm (O), 50 µm (D, E, G, and insert of L), 100 µm (F), 200 µm (P), 300 µm (C, J, M, N), 500 µm (A, B, K, L), 1 mm (H, I).
FIGURE 1 in Medusoids in the life cycle of Dentitheca dendritica (Nutting, 1900) and Nemalecium gracile sp. nov. (Cnidaria: Hydrozoa)
FIGURE 1. Dentitheca dendritica (Nutting, 1900)—fertile colony in situ (A); detail of a fertile branch showing arrangement of gonothecae (B); female (C, D) and male (E, F) gonothecae; female gonotheca seen with incident (G) and transmitted light (H), showing the terminal plate (t.p.) and the belt of refringent corpuscles (r.c.) of the medusoid; female medusoid releasing its oocytes within the gonotheca (I); eggs (e.) and developing embryo (d.e.) within the female gonotheca (J); medusoids still attached to the blastostyle after the release of the gametes in the water column (K–M). Scale bars: 100 µm (J), 200 µm (E–I, K–M), 400 µm (C, D), 2 mm (B), 3 cm (A).
Characterization Factors for the Life Cycle Assessment of Fisheries
<p>Characterization factors associated to the publication: 10.1007/s11367-023-02136-2. See the paper for detail.</p>
FIGURE 23 in A review of growth form and plant duration (life cycle) in Kalanchoe (Crassulaceae subfam. Kalanchooideae) in an evolutionary and classificatory framework
FIGURE 23. The most common whole-plant morphology found in Kalanchoe is generally expressed through a little-varying body plan that consists of a leafy, usually unbranched, stem that lengthens considerably into a stem-peduncle continuum at flowering maturity, and a terminally-borne inflorescence. Photograph: Gideon F. Smith.
FIGURE 17 in A review of growth form and plant duration (life cycle) in Kalanchoe (Crassulaceae subfam. Kalanchooideae) in an evolutionary and classificatory framework
FIGURE 17. The kalanchoes with round to obovate, soup plate-sized and -shaped leaves, i.e., those included in the southern and southtropical African K. sect. Raveta, generally have rather short internodes in the juvenile phase, so giving rise to a pseudo-rosulate architecture where a leaf cluster resembles a rosette carried close to the ground. Kalanchoe luciae is shown here. Photograph: Gideon F. Smith.
FIGURE 20 in A review of growth form and plant duration (life cycle) in Kalanchoe (Crassulaceae subfam. Kalanchooideae) in an evolutionary and classificatory framework
FIGURE 20. Kalanchoe bracteata is a much-branched, shrubby representative of the 'woody clade' of K. subg. Kalanchoe. Photograph: Gideon F. Smith.
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International Brain Laboratory public data
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OpenNeuro
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