Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
528
datasets available to search
ShareScore release 0.9.0
Dataset results
528 results for “correspondence”
Figure 8. Correspondence analysis plots. M1–M4 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 8. Correspondence analysis plots. M1–M4: moon phase classes from minimum (M1) to maximum (M4); Al1–Al4: moon altitude classes; Az1–Az4: moon azimuth classes; sw, sitand-wait; dk, doorkeeping; C, Crete; K, Koufonisi.
Figure 7. Correspondence analysis plots. A1–A4 in The foraging activity of Mesobuthus gibbosus (Scorpiones: Buthidae) in central and south Aegean archipelago
Figure 7. Correspondence analysis plots. A1–A4: air temperature classes from minimum (A1) to maximum (A4); H1–H4: air relative humidity classes; S1–S4: soil temperature classes; W1– W4: wind speed classes; M1–M4: moon phase classes; sw, sit-and-wait; dk, doorkeeping; C, Crete; K, Koufonisi.
Age- and sex-dependent variation in relatedness corresponds to reproductive skew, territory inheritance and workload in cooperatively breeding cichlids
<p>Kin selection plays a major role in the evolution of cooperative systems. However, many social species exhibit complex within-group relatedness structures, where kin selection alone cannot explain the occurrence of cooperative behaviour. Understanding such social structures is crucial to elucidate the evolution and maintenance of multi-layered cooperative societies. In lamprologine cichlids, intragroup relatedness seems to correlate positively with reproductive skew, suggesting that in this clade dominants tend to provide reproductive concessions to unrelated subordinates to secure their participation in brood care. We investigate how patterns of within-group relatedness covary with direct and indirect fitness benefits of cooperation in a highly social vertebrate, the cooperatively breeding, polygynous lamprologine cichlid Neolamprologus savoryi. Behavioural and genetic data from 43 groups containing 578 individuals show that groups are socially and genetically structured into subgroups. About 17% of group members were unrelated immigrants, and average relatedness between breeders and brood care helpers declined with helper age due to group membership dynamics. Hence the relative importance of direct and indirect fitness benefits of cooperation depends on helper age. Our findings highlight how both direct and indirect fitness benefits of cooperation and group membership can select for cooperative behaviour in societies comprising complex social and relatedness structures.</p>
2D Macro-XRF to reveal redacted sections of French queen Marie-Antoinette secret correspondence with Swedish count Axel von Fersen
<p>During the French Revolution, Marie-Antoinette, queen of France and wife of Louis the XVIth, maintained a highly secret correspondence with the Swedish count Axel von Fersen, her close friend and rumored lover. An unidentified censor later redacted certain sections of the exchanged letters. This presumably sensitive content has been puzzling historians for almost 150 years. We report on the methodology that successfully unraveled this historical mystery. X-ray fluorescence spectroscopy was used in macro scanning mode on the redacted sections. Specific data processing was applied to improve the legibility of the hidden writings (elemental ratios, statistical data reduction, multimodal images fusion, unmixing procedure; image treatments). This methodology successfully revealed the redacted contents of 8 letters, shedding new lights on Marie-Antoinette and Fersen relationship but also on the author of the redactions. It will also be of great interest for other historical and forensic cases involving the disentanglement of superimposed multi-elemental materials.</p>
Fig.11 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig.11. Genital exoskeleton of Nannochorista andina (Mecoptera:Nannochoristidae); for musculature, refer to Mickoleit (2008) and see Fig. 1. A, genital appendages, dorsal view.B, genital appendages, ventral view.C, D, right coxopod and sperm pumping complex, dorsolateral oblique.EeI, sperm pumping complex:E, posterior view; F, dorsolateral oblique; G, lateral view; H, ventral view; I, ventrolateral oblique.Abbreviations: aed. apod. ¼ aedeagal apodem; CxaI ¼ gonocoxa or first gonocoxites;kam. ¼ kammersklerit; Lpe ¼ lateropenite; Pen ¼ penial sclerite; Sty ¼ gonostylus; teg. ¼ tegimen. Note: Roman numerals indicate sclerite number; addition signs indicate sclerite fusion; italicized abbreviations indicate formal names for sclerites.
Fig. 6 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 6. Genital skeletomusculature of?Dendroleon sp. (Neuroptera: Myrmeleontidae). AeC, genitalia in situ: A, dorsal; B, lateral; C, ventral. D, E, right coxopod and peniallateropenital complex, posterolateral oblique, E with lateropenites partially removed. F, part of penial-lateropenital complex, mesal (internal). G, right coxopod, mesal. H, genitalia with left coxopod removed, mesal; I, disarticulated right coxopod and penial-lateropenital complex, mesal. Abbreviations: An ¼ anus; Cxt þ Sty ¼ coxostylar composite sclerite; Lpe ¼ lateropenite; Lpedmp ¼ lateropenital dorsomedian process; Lpevll ¼ lateropenital ventrolateral lobe; Pen ¼ penial sclerite; Prct ¼ proctiger; StIX ¼ sternum IX; Sty ¼ gonostylus; TgIX þ Cxa ¼ tergocoxal composite. Muscle abbreviations indicated in Table 1.
Fig. 3 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 3. Genital skeletomusculature of Agulla sp. (Raphidioptera: Raphidiidae). AeE, segment IX, genital appendages, and proctiger: A, lateral; B, ventral; C, distal; D, tergum removed,lateral oblique; E, left half removed and proctiger partially removed, mesal. F, coxopod piece, lateral oblique. GeI, right coxopod and sternum part, mesal. Abbreviations: An ¼ anus; Cxa ¼ gonocoxa; Cxaapd ¼ coxal apodeme; Lpe ¼ lateropenite; Pen ¼ penis; Penscl ¼ penial sclerite; Prct ¼ proctiger; StIX ¼ sternum IX; Sty ¼ stylus; Styapd ¼ stylar apodeme; Stycnd ¼ stylar condyle; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1.
Fig.14 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig.14. Genital sclerites of Hystrichopsylla talpae (Siphonaptera:Hystrichopsyllidae), after Günther (1961); for musculature, see Fig.1. A, genital appendages, sternum IX, tergum IX, and proctiger. B, genital appendages, excluding tergal-coxital composite. Abbreviations: aed.apod. ¼ aedeagal apodem; aedt. ¼ aedeagaltasche; bulb.¼ bulbalis; Dstarm ¼ distal arm of sternum IX; Endph ¼ endophallus; endot.¼ endotendons; Cxa ¼ gonocoxa; Cxt ¼ gonocoxite; ham. ¼ hamulus; hypot.¼ hypotendon; inn. tub. ¼ innere tube; Llat ¼ lateral lamina of aedeagal apodem; Lmed ¼ medial lamina of aedeagal apodem; Lpe ¼ lateropenite; lun. skl. ¼ lunarsklerit; param. ¼ paramere; Pen ¼ penial sclerite; Prct ¼ proctiger; Prxarm ¼ proximal arm of coxosternum IX; StIX ¼ sternum IX; Sty ¼ gonostylus; TgIX ¼ tergum IX; virg. vent. ¼ virga ventralis; Y-skl. ¼ Y-sklerit. Note: Fragment numbers of gonocoxites and penites indicated with Roman numerals; addition signs indicate sclerite fusion.
Fig. 2 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 2. Genital skeletomusculature of Cimbex rubidus (Hymenoptera: Cimbicidae). A, tergite IX and proctiger. BeE, genital capsule: B, dorsal; C, ventral; D, lateral; E, cupula removed, lateral. FeG, right coxopod and penial sclerite: F, mesal; G, penial conjunctiva and musculature partially removed, mesal. H, right gonopod, penial musculature removed, mesal. I, volsella, mesal (dorsal). Abbreviations: An ¼ anus; Ce ¼ cercus; Cxa ¼ "basimere" (major part gonocoxa); CxtII ¼ "parossiculus" (minor part of second gonocoxital fragment); Lpe ¼ lateropenite; Lpesut ¼ lateropinial suture with ventromedial gonocoxite; Pen ¼ penis or penial sclerite; Penapd ¼ penial apodeme ("valvura"); Prct ¼ proctiger; StIX ¼ sternum IX; Sty ¼ stylus; TgIX' ¼ tergite IX; TgIX'þCxtI ¼ "cupula" (composite sclerite of tergite IX plus basal/anterior fragment of gonocoxite). Muscle abbreviations indicated in Table 1.
Fig. 8 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 8. Genital skeletomusculature of Hypera cf. postica (Coleoptera: Curculionidae). AeD, genitalia in situ within terminal abdominal segments: A, dorsal; B, lateral, left side, sternal-coxital muscle partially removed;C, ventral;D, lateral, right side. E, J, coxites I encircling coxites II and stylar composite,lateral,with sternum removed in E which shows the left side. FeJ, coxopenis (coxital-penial composite, CxtII þ Pen): F, endophallus partially exserted, ventrolateral oblique; G, dorsal; H, ventral; I, sternum in place, right side; J, ventrolateral oblique. Abbreviations: CxtI ¼ "phallobase" (first gonocoxites); CxtII þ Pen ¼ coxopenial composite; Endscl ¼ endophallic sclerite; StVIII ¼ sternum VIII; StIX ¼ sternum IX; Stap ¼ sternal apophysis; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1.
Fig. 13 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 13. Genital skeletomusculature of Panorpa nuptialis (Mecoptera: Panorpidae). A, genitalia in situ, lateral. B, composite sclerite of tergum and sternum IX. CeE, genital appendages: C, dorsal; D, ventral; E, distal. FeH, right half of genital appendages: F, dorsolateral oblique; G, lateral, paired appendages of sperm pumping complex intact; H, lateral, left half of sperm pumping complex removed. I, J, mittelplatte and dorsal pseudoparameres (¼ kammersklerit plus second fragment of aedeagal apodem). K, pistilltrö ager, ventrolateral oblique.L, base of dorsal pseudoparameres, posterior view.M, base of dorsal pseudoparameres, internal (anterior) view. Abbreviations: Apd ¼ apodeme of pistilltrö ager; Ce ¼ cercus;d. ps. par. ¼ dorsal pseudoparamere; Cxa ¼ gonocoxa or first gonocoxites; Cxt ¼ gonocoxite; CxtAapd ¼ anterior apodeme of gonocoxite; CxtDapd ¼ dorsal apodeme of gonocoxite; mittelp. ¼ mittelplatte; pistillt. ¼ pistilltrö ager; Pen ¼ penis or penial sclerite; Prct ¼ proctiger; StIX ¼ sternum IX; Sty ¼ gonostylus; StyDcond ¼ dorsal stylar condyle; StyVcond ¼ ventral stylar condyle; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1. Note: Sclerite fragment numbers indicated with Roman numerals; addition signs indicate sclerite fusion.
Fig. 10 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 10. Genital skeletomusculature of Mengenilla sp. (Strepsiptera: Mengenillidae), modified from Hünefeld, Pohl, et al. (2011b). A, abdominal segment IX and proctiger in cross-section. Abbreviations: Cxa ¼ gonocoxa; Pen ¼ penis; Prct ¼ proctiger; StIX ¼ sternum IX; Stap ¼ sternal apodeme; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1.
Fig. 9 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 9. Genital skeletomusculature of Ilybius biguttulus (Coleoptera:Dytiscidae). AeD, genitalia in situ: A, dorsal; B, dorsolateral oblique; C, ventral; D, dorsal, tergal-coxital muscles removed.EeG, genitalia and anterior fragment of sternum IX (sternal apodeme): E, ventral; F, ventral,sternal muscle removed;G, dorsal.H, coxital-stylar composite sclerites spread away from coxopenis (composite of second coxites and penis, CxtII þ Pen), dorsolateral oblique. I, coxopenis, left side, lateral. Abbreviations: CxtI þ Sty ¼ coxostylar composite sclerite; CstII þ Pen ¼ coxopenial composite; Endscl ¼ endophallic sclerite; StIX ¼ sternum IX; Stap ¼ sternal apodeme; Styapd ¼ stylar apodeme; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1.
Fig. 7 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 7. Genital skeletomusculature of Cantharis (Cantharis) (Coleoptera: Cantharidae). A, B, genitalia in situ: A, lateral; B, ventral. CeN, genitalia various aspects and states of dissection: C, whole, dorsal; D, E, stylus and muscle partially removed, dorsal; F, whole, ventral; G, dorsal portion of stylus removed, lateral; H, full stylus and part of penial sclerite removed; I, whole, ventrolateral oblique; J, stylus and muscle partially removed, dorsal; K, L, stylus partially removed, with K in ventrolateral oblique view, L in lateral view; M, N, coxites II and penial sclerite,partially dissected, with M in dorsal view, N in mesal (lateral) view.Abbreviations: CxtSty-art ¼ gonocoxite IIestylar articulation; Cxtpdp ¼ gonocoxite II posterodorsal process; CxtI ¼ "phallobase" (first gonocoxites); CxtII ¼ second gonocoxites (continuous with penis, forming "coxopenis" or CxtII þ Pen); Cxttvl ¼ gonocoxite II transverse lamella; Cxtvma ¼ gonocoxite I ventromedial apodeme; Pen ¼ penis and penial sclerite (continuous with CxtII, forming "coxopenis" or CxtII þ Pen); StIX ¼ sternum IX; Stap ¼ sternal apophysis; Sty ¼ gonostylus; Stydl ¼ gonostylar dorsal lobe; Stypdp ¼ gonostylar prosterodorsal process; Styvt ¼ gonostylar ventral tine; TgIX ¼ tergum IX; Tgap ¼ tergal apophysis. Muscle abbreviations indicated in Table 1.
Fig.16 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig.16. Genital skeletomusculature of Pycnopsyche antica (Trichoptera: Limnephilidae).A, genital and pregenital segments, lateral.B, genital and postgenital segments, posterior.C, same as B, left coxopod removed. D, same as C, lateral oblique. E, genital and postgenital segments, ventral. F, genital appendages, dorsolateral oblique. G, same as F, left gonopod removed. H, right gonopod and piece of postgenital complex, muscles removed, mesal (medial). IeK, penial sclerite and lateropenites: I, dorsolateral; J, dorsolateral, sheath membrane removed; K, ventrolateral, base of penial sclerite torn open. Abbreviations:?Ce ¼ structures possibly homologous with cerci; Cxa ¼ gonocoxa; Lpe ¼ lateropenite; Pen ¼ penis or penial sclerite; Prct ¼ proctiger; Seg ¼ segment; St ¼ sternum; Sty ¼ gonostylus; Tg ¼ tergum.Muscle abbreviations indicated in Table 1. Note: Segment numbers indicated with Roman numerals; addition signs indicate sclerite fusion.
Fig. 17 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig. 17. Key skeletomuscular morphological apomorphies of genitalia here inferred, mapped on the phylogenetic chronogram of the Hexapoda pruned to the specific terminals compared in the present study (tree modified from Misof et al., 2014). Bayesian analysis may provide estimates of rate and timing of inferred transformations.1. Hexapoda: male gonopore(s) situated on a lateromedially-undifferentiated gonopod (the penis). 2. Protura: male gonopores situated on distal (second) endopodal segment. 3. Collembola, Diplura: penes independently reduced to papillae. 4. Ectognatha: male and female genitalia derived from appendages (primary and secondary gonopods) of two successive segments. 5. Ectognatha: male phallic complex reduced to single, simple structure (the penis), modified from gonopores of abdominal segment X. 6. Dicondylia: dorsoventral penial extrinsic muscle lost. 7. Gonapophyses (endopods of coxopods IX) probably lost once in the Odonatoptera (along stem to Odonata) and once or twice in the Chiastomyaria. 8. Odonata: plesiomorphic condition of gamete transfer via spermatophore retained, although the latter is deposited in the autapomorphic secondary genitalia. 9. Ephemeroptera, Neoptera: sperm directly deposited in the female via intromission of the penis.10. Ephemeroptera: gonopods derive multiannulate styli.11. Ephemeroptera: penis laterally articulated with tergum IX, bearing derived tergopenial musculature. 12. Neoptera: sternopenial muscle duplicated, resulting in novel penial promotor. 13. Polyneoptera: secondary gonopods (coxopods IX) not incorporated into penial ("phallic") complex, being rather (usually) undifferentiated from sternum IX.14. Two independent lines of increasing complexity and disparity observed in the penial complex of Polyneoptera, once for the Zoraptera, the other for the Orthopterida (i.e., core Polyneoptera). 15. Two independent lines of penial complex simplification observed in Polyneoptera, once for the Plecoptera, the other for the Dictyoptera (namely, reduction observed in Isoptera).16. Grylloblattodea: coxopods IX secondarily differentiated from sternum IX.17. Eumetabola: gonostyli strengthened for clasping, bearing differentiated abductor and adductor muscles.18. Condylognatha: dorsal extrinsic penial muscle gained. 19. Hemiptera: gonopods undifferentiated from fused tergum and sternum IX, forming pygophore; pygophore also bearing origins of the penial extrinsic muscles. 20. Endopterygota: penis completely integrated with gonopods developmentally and gonopods, as in Hemiptera, bear the origins of the penial extrinsic muscles. 21. Endopterygota: penial musculature is duplicated dorsoventrally, resulting in greater functional potential of copulatory apparatus (penial-gonopodal complex). 22. Endopterygota: lateropenite ("parandrite" or "paramere" sensu Verhoeff) uniquely derived from penial sclerite (skeletomusculature of Psocodea in need of renewed study).23. Hymenoptera: origin of cupula (¼ "basal ring"), which controls overall motion of gonopods. 24. Hymenoptera: parossiculus derived from ventromedial gonocoxa, forming volsellar complex with lateropenite ("digitus"). 25. Sialida (sensu Bodreaux,1979 modified from Handlirsch,1908): gonocoxae migrated dorsally, fusing with tergum IX over the penis. 26. Sialida: external gonopore dissociated from the penial sclerites (probably in correlation with female loss of ovipositor). 27. Coleopterida: lateropenite lost. 28. Strepsiptera: genitalia reduced, with only a penis (or coxopenis) expressed. 29. Coleoptera: ancestral gonocoxa divided into two parts: the first or anterior gonocoxites ("phallobase") bearing the insertions of the extrinsic gonopodal musculature, the second or posterior gonocoxites incorporated to completely integrated with the penis (forming "coxopenis"); gonostyli variably associated with phallobase. 30. Euantliophora: genitalic complexity increases to extreme degree, extant taxa inheriting an autapomorphic aedeagal apodem (present in Siphonaptera and Nannochoristidae). 31. Siphonaptera: gonopodites, bearing styli, fused with tergo-proctiger complex. 32. Siphonaptera: sternum IX with lateral elongate arms. 33. Siphonaptera: sperm-pumping complex significantly modified. 34. Mecoptera: sperm-pumping complex with mittelplatte (note uncertainty of homology for boreid penial sclerites).35. Boreidae: sperm-pumping complex reduced, most slerites lost. 36. Boreidae: spermatophore regained. 37. Pistillifera: pistilltrö ager derived in sperm-pumping complex. 38. Diptera: partial to complete integration of sternum IX with gonopods; increasing genitalic complexity observed. 39. Amphiesmenoptera with relatively unmodified genitalia, although Lepidoptera with lateromedially fused lateropenites ("median plate") and enlarged and unmusculated gonostylus.
Fig.12 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig.12. Genital skeletomusculature of Apterobittacus apterus (Mecoptera:Bittacidae).AeC, genital and pregenital segments: A, lateral; B, distal; C, ventral.DeG, genital appendages and sternum IX: D, dorsal; E, lateral (partially dissected); F, lateral, left fragment of first coxite removed; G, same as F, with more muscle removed. H, left fragment of first coxite, mesal. IeN, complex of second coxite, lateropenite, and penial sclerite: I, lateral, first penial sclerite fragment removed; J, dorsal; K, dorsal, first penial sclerite fragment removed, dorsal.L, second coxites and first penial sclerite fragment removed,dorsal. M, same as L, dorsolateral oblique. N, first penial fragment,ventral (mesal), left and median tines partially broken. Abbreviations: Apd ¼ apodeme; Ce ¼ cercus; Cxa ¼ gonocoxa or first gonocoxites; Cxt# ¼ gonocoxite fragment; Lpe ¼ lateropenite; Pen# ¼ penial sclerite fragment; Prct ¼ proctiger; Sclbr-b-a'' ¼ sclerotic bridge between mittelplatte and second fragment of aedeagal apodem; Sclbr-cxt-cxt ¼ sclerotic bridge between first gonocoxites; SegVII ¼ seventh abdominal segment; Seg VIII ¼ abdominal segment VIII; StIX ¼ sternum IX; Sty ¼ stylus; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1. Note: Sclerite fragment numbers indicated with Roman numerals; addition signs indicate sclerite fusion.
Fig.15 in A general theory of genital homologies for the Hexapoda (Pancrustacea) derived from skeletomuscular correspondences, with emphasis on the Endopterygota
Fig.15. Genital skeletomusculature of Tipula (Hesperotipula) californica (Diptera:Tipulidae). AeE, whole genitalia: A, lateral; B, dorsal; C, posteroventral oblique; D, distal; E, distal, tergum and sternum IX removed. F, tergum IX, mesal (ventral). GeI, genitalia with tergum IX and left gonopod removed, dorsolateral: G, with proctiger; H, proctiger partially removed; I, proctiger completely removed. JeL, right coxopod: J, K, mesal (medial); L, distal, oblique. M, genitalia with tergum IX and left coxopod removed, dorsolateral. N, right coxopod and penial sclerites, mesal. O, penial sclerites, lateral. Abbreviations: Ce ¼ cercus; Cxa ¼ gonocoxa; Lpe ¼ lateropenite; Pen ¼ penis; PenI ¼ first penial sclerite; PenI- nd ¼ penial needle; PenII ¼ second penial sclerite; PenIIdt ¼ dorsal tines of second penial sclerite; PenIImd ¼ medial disc of second penial sclerite; PenIII ¼ third penial sclerite; Prct ¼ proctiger; StVIII ¼ sternum VIII; StIX ¼ sternum IX; St-br ¼ sternal bridge; StCxa-sut ¼ sternocoxal suture; Sty ¼ gonostylus; Sty-dt ¼ dorsal tine of gonostylus; Sty- rcpt ¼ stylar receptor; Sty-vt ¼ ventral tine of gonostylus; TgIX ¼ tergum IX. Muscle abbreviations indicated in Table 1.
Sources of PM2.5-associated Health Risks in Europe and Corresponding Emission-induced Changes during 2005-2015
<p>-New data generated for 2022GH000767</p> <p>-Including the calculated sensitivities of the total PM2.5-related premature deaths in Europe to anthropogenic emissions of SO2, NOx, NH3, OC, BC, and secondary organic aerosol precursors (SOAP) in 2015</p> <p>-Including the simulated annual mean PM2.5 exposure and PM2.5-related premature death in 2015 from the base simulation and the sensitivity experiment in which all inputs of the boundary conditions were reduced by 20% (BC20), respectively. </p> <p>-All the data were generated by the GEOS-Chem model and its adjoint</p>
Corresponding Dataset for Precision of Spacecraft Doppler Tracking at Low Signal-to-Noise Ratios
<p><br> Corresponding Dataset for Precision of Spacecraft <br> Doppler Tracking at Low Signal-to-Noise Ratios<br> README FILE<br> Dustin Buccino<br> January 1, 2023<br> Jet Propulsion Laboratory<br> California Institute of Technology</p> <p>=============================================================================<br> INTRODUCTION<br> =============================================================================</p> <p> This dataset contains open-loop data collected by the Planetary Radar<br> and Radio Science Group at the Jet Propulsion Laboratory from the Low-SNR<br> Ground System Demonstration with DSS-25 in May 2020. Futhermore, it<br> also provides the necessary data behind the figures in the corresponding<br> publication. This dataset is provided in order to supplement the submitted<br> article to the "Radio Science" journal</p> <p> Buccino, D.R., et al (2023), Precision of Spacecraft Doppler Tracking <br> at Low Signal-to-Noise Ratios, Radio Science, submitted<br> January 2023.</p> <p>=============================================================================<br> ARCHIVE INFORMATION<br> =============================================================================</p> <p> This archive contains several data types, located within subdirectories.<br> <br> ROOT<br> `- 159TEST2022133_1845X25X25RO.A02_XATnn_nndBHz<br> <br> These files are the open-loop data collected at the DSN <br> during the test. There are six files, one for each SNR level. The<br> files are in the DSN-standard 0159-Science format (binary data).<br> To decode these files, one should utilize the software <br> interface specification documents from the Planetary Data System<br> radio science documentation bundle:</p> <p> https://pds-geosciences.wustl.edu/<br> radiosciencedocs/urn-nasa-pds-radiosci_documentation/<br> <br> `- figures.zip<br> <br> This directory contains all data necessary to reproduce the figures<br> in the publication. Data include Doppler residuals, SNR measurement,<br> Allan deviation and associated parameters. Each file in this <br> directory is plain-text.</p> <p>=============================================================================<br> ACKNOWLEDGMENTS<br> =============================================================================</p> <p>This work was carried out at the Jet Propulsion Laboratory, <br> California Institute of Technology, under contract with the National <br> Aeronautics and Space Administration. Government sponsorship acknowledged.</p> <p>=============================================================================<br> PRIMARY POINT OF CONTACT<br> =============================================================================</p> <p>Dustin Buccino<br> Jet Propulsion Laboratory<br> Planetary Radar and Radio Sciences<br> (818) 393 - 1072<br> Dustin.R.Buccino@jpl.nasa.gov</p> <p>=============================================================================<br> ACRONYMS AND ABBREVIATIONS<br> =============================================================================</p> <p> ASCII American Standard Code for Information Interchange<br> DOY Day of year<br> DSN Deep Space Network<br> JPL Jet Propulsion Laboratory<br> NAIF Navigation Ancillary Information Facility<br> NASA National Aeronautics and Space Administration<br> PDS Planetary Data System<br> RS Radio Science<br> RSS Radio Science Subsystem<br> SIS Software Interface Specification<br> TXT Text file<br> UTC Universal Time, Coordinated<br> </p>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.