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44 results for “Chang`e 5”
Chang'e 5 RF recording at 8486.2 MHz with Allen Telescope Array on 2020-12-19 (X polarization)
<p>This dataset contains a recording of X-band telemetry signals from the Chinese lunar sample retrieve mission Chang'e 5 done on 2020-12-19, after the Earth flyby, in a direct trajectory to the Sun-Earth L1 Lagrange point. The recording was done at Allen Telescope Array using antenna 2h in dual XY (linear) polarization.</p> <p>The hardware configuration was as follows: antenna 2h was connected to RFCB LO d, which was tuned to a frequency of 8475 MHz and used an output IF of 512 MHz. A USRP N321 was connected to the IF output of the RFCB and digitized both polarizations. The USRP used external 10 MHz reference and PPS coming from the observatory distribution system. The IQ sample rate of the USRP was 30.72 Msps and a GNU Radio flowgraph was used to channelize four frequencies from the spacecraft (8463.7, 8471.2, 8478.6 and 8486.2 MHz), using an IQ sample rate of 480 ksps for each channel. Only the 8471.2 MHz and 8486.2 MHz channels contains signals from the spacecraft.</p> <p>The GNU Radio flowgraph stored the IQ data for each channel as 32-bit floats in the <a href="https://wiki.gnuradio.org/index.php/Metadata_Information">GNU Radio metatata file format</a>, with detached headers. After recording, the data was converted 16-bit integers and <a href="https://github.com/gnuradio/SigMF">SigMF</a> format.</p> <p>This dataset contains the IQ data for the channel at 8486.2 MHz, in SigMF format. Each polarization is in a different file. The original metadata headers are also provided. This dataset contains the X polarization. The Y polarization can be found in "<a href="https://zenodo.org/record/4405179">Chang'e 5 RF recording at 8486.2 MHz with Allen Telescope Array on 2020-12-19 (Y polarization)</a>".</p>
Supplementary material 5 from: Dickey JWE, Cuthbert RN, Rea M, Laverty C, Crane K, South J, Briski E, Chang X, Coughlan NE, MacIsaac HJ, Ricciardi A, Riddell GE, Xu M, Dick JTA (2018) Assessing the relative potential ecological impacts and invasion risks of emerging and future invasive alien species. NeoBiota 40: 1-24. https://doi.org/10.3897/neobiota.40.28519
Outlining RIP and RIR data :
Supplementary material 5 from: Bogataj U, Praznik M, Mrak P, Štrus J, Tušek-Žnidarič M, Žnidaršič N (2018) Comparative ultrastructure of cells and cuticle in the anterior chamber and papillate region of Porcellio scaber (Crustacea, Isopoda) hindgut. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 427-458. https://doi.org/10.3897/zookeys.801.22395
SI Figure 5. Boxplots depicting individual measurements of basal membrane labyrinth depth :
Figure 5 from: Wood CT, Nihei SS, Araujo PB (2018) Woodlice and their parasitoid flies: revision of Isopoda (Crustacea, Oniscidea) – Rhinophoridae (Insecta, Diptera) interaction and first record of a parasitized Neotropical woodlouse species. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 401-414. https://doi.org/10.3897/zookeys.801.26052
Figure 5 Rhinophoridae larva obtained from the Neotropical isopod Balloniscusglaber. Morphotype 2, 3rd instar A dorsal view B detail from anterior part showing the cephaloskeleton and anterior spiracles C detail of the posterior spiracle.
Figure 3 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 3 Aggregation of isopod species differing in desiccation resistance at different temperatures. Mean ± 1 SE aggregation indices (variance:mean ratio) at 90% relative humidity. aP.scaber (F 4,249 = 3.76, p < 0.01) bA.vulgare (F 4,249 = 1.97, P < 0.01) cO.asellus (F 4, 249 = 12.22, P < 0.001) d thermal reaction norms for aggregation expressed as quadratic response curves for: P.scaber (dashed line): y = -11.519 + 1.526× - 0.04×2; A.vulgare (solid line): y = -3.534 + 0.574× 0.016×2; O.asellus (dotted line): y = -5.890 + 0.814× – 0.018×2.
Figure 4 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 4 Moisture reaction norms for a) sheltering and b) feeding behaviours with changing sand moisture content (time spent in behaviour as percentages of total observed behaviours). Lines represent linear regression models: A.vulgare (solid line) (sheltering: y = 95.24 – 1.05×; feeding: y = 0.32 + 0.03), P.scaber (dashed line) (sheltering: y = 96.72 – 0.19×; feeding: y= 0.22 + 0.05×), Ph.muscorum (dotted line) (sheltering: y = 93.14 – 2.16×; feeding: y = 0.36 + 0.55x). Further regression statistics and number of observations (N), are given in Table 1.
Figure 5 from: Shultz JW (2018) A guide to the identification of the terrestrial Isopoda of Maryland, U.S.A. (Crustacea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 207-228. https://doi.org/10.3897/zookeys.801.24146
Figure 5 Oniscidae, Philosciidae, Halophilosciidae, Ligiidae. AOniscidae: OniscusasellusB–EPhilosciidaeB–CPhilosciamuscorumB dorsal view C pleotelson DChaetophilosciasicula: dorsal view of pleon (after Vandel 1962: figure 247) ELittorophilosciavittata: pleotelson, dorsal view F–GLigiidaeFLigiaexoticaGLigidiumelrodii. Scale bars: 5 mm.
Figure 2 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 2 A schematic representation of a typical thermal response curve for enzymes (simplified from Huey and Kingsolver 1989). The temperature optimum is the temperature at which performance reaches its maximal level or peak performance. The performance breadth defines how steeply peaked (stenothermal) or broadly plateaued (eurythermal) the response curve is. Any part or the whole of such a curve can be considered to be a reaction norm of a genotype representing a range of phenotypes expressed across an environmental gradient, in this example, of temperature.
Figure 5 from: Taiti S, Argano R, Marcia P, Scarpa F, Sanna D, Casu M (2018) The genus Alpioniscus Racovitza, 1908 in Sardinia: taxonomy and natural history (Isopoda, Oniscidea, Trichoniscidae). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 229-263. https://doi.org/10.3897/zookeys.801.24102
Figure 5 Alpioniscusonnisi Taiti & Argano, sp. n. from Grotta Giuanniccu Mene, ♂ paratype: A adult specimen, dorsal B dorsal scale-seta C cephalon, frontal D cephalon, dorsal E pleonites 4, 5, telson and uropods F antennula G antenna.
Figure 1 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 1 A conceptual diagram illustrating some of the pathways by which changes in global climate could potentially impact on rates of carbon dioxide emissions from soils. Both changes in temperature and in the levels and patterns of rainfall have strong direct effects on the metabolism of bacteria and fungi but their ecology and metabolism are also regulated by the extent to which they are stimulated by soil animals. Both functional (e.g., behavioural and physiological) responses and numerical (both life history and population) responses of soil animals are affected by their microclimate. This is in turn affected by larger scale changes in temperature and rainfall. Therefore, as well as their direct effect on microbial metabolism, these climatic variables have a strong indirect effect by influencing the behavioural, physiological, life history, and population processes of soil animals such as isopods.
Figure 5 from: Souty-Grosset C, Faberi A (2018) Effect of agricultural practices on terrestrial isopods: a review. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 63-96. https://doi.org/10.3897/zookeys.801.24680
Figure 5 Land cover map with sampling sites in Plaine Mothaise, central-western France. Land cover features of the study site were determined using aerial photographs (Google Earth) and field inspections. Linear characteristics from the landscape were distinguished such as riparian, hedge, continuous and intermittent vegetation. The final categories obtained are Cultivation (crops), Grassland, Poplars, Types of connection, roads and urban. Landscapes were mapped using Arcmap 9.3 (ESRI, 2004) as a main geographical information system. Black dots indicate sites of pitfall trap sampling.
Figure 6 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 6 Thermal reaction norm gradients for evaporation rate (water loss) for isopods from biomes differing in availability of moisture. Evaporation rate (g g-1 h-1× 10-2) standardised to a temperature range of 3.5 °C (from Edney 1951; Warburg 1965, 1987, 1989). Key to species: Lo Ligiaoceanica, Ph Philosciamuscorum, Oa Oniscusasellus, Ps Porcellioscaber, Av Armadillidiumvulgare, Ao Armadilloofficinalis, Aa Armadilloalbomarginatus, Po Porcellioolivieri, An Armadilliumnasatum, Ba Buddelundiaalbinogrisescens, Bf Buddelundiafrontosa, Va Veneziilloarizonicus, Bsp Buddelundia spp. probably lateralis, Hr Hemilepistusreaumurii, Sf Schizidiumfestai. Key to habitats: littoral (blue), mesic (green), xeric (yellow), semi-arid (orange) habitats in South Australia.
Figure 5 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 5 Gradients of moisture reaction norms for respiration of isopods differing in their resistance to desiccation. Reaction norms over the range 50–100% relative humidity for respiratory rates measured as rates of oxygen uptake (mm3 mm-2 body surface h-1) (Edney 1968). Key to species: Lo Ligiaoceanica, Oa Oniscusasellus, Ps Porcellioscaber, Av Armadillidiumvulgare. Key to habitats: littoral (blue), mesic (green).
Figure 5 from: Nako J-D, Lee NS, Wright JC (2018) Water vapor absorption allows for volume expansion during molting in Armadillidium vulgare and Porcellio dilatatus (Crustacea, Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 459-479. https://doi.org/10.3897/zookeys.801.23344
Figure 5 Mean masses of Ligidiumlapetum in 100% RH. The mean mass of the surviving animals on Day 2 is the mean % mass loss of those animals, subtracted from the mean of all animals at Day 0. No animal survived to Day 3 or initiated ecdysis.
Figure 5 from: Gongalsky KB, Turbanov IS, Medvedev DA, Volkova JS (2018) Description of a new species of the genus Protracheoniscus Verhoeff, 1917 and redescription of Protracheoniscus kryszanovskii Borutzky, 1957 from the southeast of European Russia (Isopoda, Oniscidea, Agnaridae). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 189-205. https://doi.org/10.3897/zookeys.801.23167
Figure 5 Protracheoniscuspokarzhevskii sp. n.: A exopod of pleopod 1 B endopod of pleopod 1 C exopod of pleopod 2 D endopod of pleopod 2 E exopod of pleopod 3 F exopod of pleopod 4 G exopod of pleopod 5 H genital papilla (male, paratype).
Figure 5 from: Sfenthourakis S, Hornung E (2018) Isopod distribution and climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 25-61. https://doi.org/10.3897/zookeys.801.23533
Figure 5 The relative contribution of different species' categories in the isopod faunas of selected European countries.
Figure 5 from: Kashani GM, Abedini A, Montesanto G (2018) Terrestrial isopods of the family Eubelidae Budde-Lund, 1899 from Iran, with description of a new species (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 177-187. https://doi.org/10.3897/zookeys.801.23340
Figure 5 Koweitoniscusshafieii sp. n., male, paratype. A pereopod 1 B pereopod 7 C pleopod 1 endopodite with enlarged apex D pleopod 1 exopodite E pleopod 2 F pleopod 3 exopodite G pleopod 4 exopodite H pleopod 5 exopodite.
Figure 5 from: Csonka D, Halasy K, Buczkó K, Hornung E (2018) Morphological traits – desiccation resistance – habitat characteristics: a possible key for distribution in woodlice (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 481-499. https://doi.org/10.3897/zookeys.801.23088
Figure 5 Intrageneric (between the two specimens per species) comparison of tergal cuticle thickness in four Armadillidium species (2 specimens/species, 5 slides/specimen, 10 measurements/slide). [Measures: median ± first quartile and max/min (Species names as in Figure 3)].
Figure 5 from: Bogataj U, Praznik M, Mrak P, Štrus J, Tušek-Žnidarič M, Žnidaršič N (2018) Comparative ultrastructure of cells and cuticle in the anterior chamber and papillate region of Porcellio scaber (Crustacea, Isopoda) hindgut. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 427-458. https://doi.org/10.3897/zookeys.801.22395
Figure 5 Cuticle and basal lamina thickness in the two hindgut regions. Median values of cuticle thickness (A) and basal lamina thickness (B) in cells from the anterior chamber (blue) and the papillate region (red) of three specimens.
Figure 5 from: De Smedt P, Boerave P, Arijs G, Segers S (2018) Woodlice of Belgium: an annotated checklist and bibliography (Isopoda, Oniscidea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 265-304. https://doi.org/10.3897/zookeys.801.21894
Figure 5 Six of the nine species added to this new checklist, aPorcelliomonticolabElumacaelatacHyloniscusripariusdTrichoniscoidessarsiePhilosciaaffinis and fMetatrichoniscoidesleydigii; photos: Gert Arijs.
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