Littérature scientifique sur le sujet « Ursinia »

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Articles de revues sur le sujet "Ursinia"

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Shivas, R. G. « Puccinia ursiniae sp. nov. on Ursinia anthemoides ». Mycological Research 95, no 3 (mars 1991) : 379–81. http://dx.doi.org/10.1016/s0953-7562(09)81255-0.

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Magee, A. R., J. Poovan, L. Mucina et J. S. Boatwright. « Taxonomy of Ursinia subgenus Ursinia (Asteraceae, Anthemideae) ». South African Journal of Botany 103 (mars 2016) : 325. http://dx.doi.org/10.1016/j.sajb.2016.02.081.

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Herman, P. P. J. « ASTERACEAE : A NOTE ON URSINIA BRACHYLOBA ». Bothalia 25, no 2 (9 octobre 1995) : 244. http://dx.doi.org/10.4102/abc.v25i2.736.

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Magee, Anthony Richard, JAMES S. BOATWRIGHT et LADISLAV MUCINA. « Four new species of Ursinia (Asteraceae, Anthemideae) from South Africa, with an updated key to the genus in Namaqualand ». Phytotaxa 177, no 3 (29 août 2014) : 137. http://dx.doi.org/10.11646/phytotaxa.177.3.1.

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Recent field and herbarium studies of the southern African genus Ursinia (Anthemideae, Asteraceae) in Namaqualand, South Africa, have revealed greater morphological variability than currently accommodated and a high percentage of misidentified specimens. In an attempt to remedy this we herein describe four new species (Ursinia arida, U. glandulosa, U. kamiesbergensis and U. laciniata) and provide a key to the species in the region, together with illustrations of their involucral bracts and paleae. The species can be distinguished by a combination of their life history, vestiture, presence or absence of appendages on the paleae, and shape of the involucral bracts and their scarious apices.
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Swelankomo, N., L. Mucina et P. P. J. Herman. « Phenetic classification of cypselae in Ursinia (Anthemideae, Asteraceae) ». South African Journal of Botany 73, no 2 (avril 2007) : 316. http://dx.doi.org/10.1016/j.sajb.2007.02.127.

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Kroszczyṅski, Wojciech, Włodzimierz M. Daniewski, Miloš Buděšínský, David Šaman, Halina Grabarczyk, Bohdan Drożdż et Miroslav Holub. « Minor sesquiterpenic lactones from Ursinia anthemoides (L.) POIRET ». Collection of Czechoslovak Chemical Communications 50, no 1 (1985) : 94–102. http://dx.doi.org/10.1135/cccc19850094.

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The authors isolated from the aerial parts of Ursinia anthemoides (L.) POIRET another five sesquiterpenic lactones, IV, V, VII, IX and X and have derived for them their structures and configurations mainly on the basis of 1H NMR spectroscopy and CD measurements; for compounds IV and V absolute configurations have also been proposed.
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Jakupovic, J. « Sesquiterpene lactones and other constituents from Ursinia species ». Phytochemistry 31, no 2 (mars 1992) : 863–80. http://dx.doi.org/10.1016/0031-9422(92)80176-f.

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Jakupovic, J., U. Ganzer, P. Pritschow, L. Lehmann, F. Bohlmann et R. M. King. « Sesquiterpene lactones and other constituents from Ursinia species ». Phytochemistry 31, no 3 (mars 1992) : 863–80. http://dx.doi.org/10.1016/0031-9422(92)80030-i.

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Steyn, H. M. « Faktore wat die fenologie van Ursinia cakilefolia, ’n efemeer van Namakwaland, beïnvloed ». Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie 15, no 3 (11 juillet 1996) : 109–15. http://dx.doi.org/10.4102/satnt.v15i3.642.

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The aim of this study was to investigate the effect of temperature and sowing date on the phenology of Ursinia cakilefolia, a Namaqualand ephemeral species. Seeds were sown on different dates and plants were subjected to various temperature treatments. Sowing date had a distinct effect on the growth and phenology of the plants. From the results it seems that temperature plays an important role in the timing of phenological stages. However, the effect of temperature differed between sowing dates. The plant's response to temperature is apparently modified by the prevailing photoperiod, although it may also be due to an endogenous rhythm. Generally it seems as if plants require cold temperatures from sowing until the initiation of flower buds, after which the plants need heat for anthesis and further development.
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Beneke, Karen, Irmgard von Teichman, Margaretha W. van Rooyen et G. K. Theron. « Fruit polymorphism in ephemeral species of Namaqualand. II. Anatomical differences between polymorphic diaspores of Arctotis fastuosa and Ursinia cakilefolia ». South African Journal of Botany 58, no 6 (décembre 1992) : 456–60. http://dx.doi.org/10.1016/s0254-6299(16)30792-x.

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Thèses sur le sujet "Ursinia"

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Swelankomo, Nonkululeko. « Molecular phylogeny, radiation patterns and evolution of life-history traits in Ursinia (Anthemideae, Asteraceae) ». Thesis, Stellenbosch : Stellenbosch University, 2008. http://hdl.handle.net/10019.1/1793.

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Thesis (MSc (Botany and Zoology))--Stellenbosch University, 2008.
Sequence data from the Internal Transcribed Spacer (ITS) of the nuclear ribosomal DNA were used to study the phylogenetic relationships in the genus Ursinia Gaertn. (Asteraceae, Anthemideae) in the southern African region. Closely related genera, i.e. Cotula L., Osteospermum L. and Agoseris Raf., were used as outgroups. The study also included maximum parsimony and principal component analyses. The taxa within the genus Ursinia had previously been classified into two subgenera, Ursinia and Sphenogyne R.Br., mainly on the basis of distinct cypsela characters. The maximum parsimony, principal component and the phylogenetic analyses revealed two subgenera, corresponding to the existing subgeneric classification. Principal component analysis shows that the pappus, the number of pappus bristles and the colour of the cypsela are the most informative characters. However, the low number of phylogenetically informative characters of the ITS sequences, the poor resolution in the consensus tree, and low branch support values indicate that the ITS data contain weak phylogenetic signals. The low bootstrap values for many nodes suggest that one should be cautious in using the ITS region alone to make final conclusions about the origin and evolution of taxa. In maximum parsimony analysis, the RI, CI and bootstrap values are low; principal component analysis values are also low. Furthermore, there is a lack of resolution in subgenus Sphenogyne. In the literature, Ursinia is divided into seven series but they were not retrieved as monophyletic in this study, probably because of short branch lengths in the phylogeny. Further molecular data are therefore required to be able to support or reject the present classification. Maximum parsimony, principal component and molecular analyses show that U. trifida f. calva Prassler and U. trifida (Thunb.) N.E.Br. f. trifida are not sister taxa, supporting the recognition of these two taxa as separate species. The Ursinia taxa from the summer-rainfall region are not monophyletic and are sister to a clade of Cape species. This supports a hypothesis that Ursinia migrated from the Cape into the Drakensberg which has been shown for a number of other Cape groups that have Drakensberg relatives.
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Baron, Jean-Pierre. « Démographie et dynamique d'une population française de Vipera ursinii ursinii (Bonaparte, 1835) ». Paris, EPHE, 1997. http://www.theses.fr/1997EPHE3010.

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Le régime de la Vipère d'Orsini au Mont-Ventoux est pour plus de 99% constitué d'orthoptères. La taille minimale des orthoptères consommés est la même pour toutes les vipères. La période d'alimentation s'étend de la fin-juin à la fin-septembre pour tous les individus. Les immatures n'entrent en activité qu'au début de la période d'alimentation, leur période annuelle d'activité s'étend sur 3,5 mois contre 5 et 6 mois respectivement chez les femelles et les mâles adultes. Les repas sont fréquents et petits. Les femelles se nourrissent pendant la gestation. Les femelles adultes survivent mieux que les mâles. Le taux annuel de survie des immatures est élevé, du même ordre que celui des adultes. Chez les femelles, la reproduction est le plus souvent biennale ; la probabilité de survie ne dépend pas de l'état reproducteur, au contraire de la probabilité de capture. Les prises alimentaires des femelles gestantes sont souvent mises à profit pour reconstituer, au moins partiellement, les réserves consommées pour la vitellogénèse. Le nombre d'oeufs est fortement lié à la taille des femelles et la fécondité moyenne, corrigée de cette dépendance, varie significativement d'une année à l'autre sans que cela traduise une variabilité de la condition corporelle moyenne à l'ovulation. Le succès reproducteur est élevé. La masse des nouveau-nés est liée à la taille maternelle et à l'effectif de la portée, mais pas à la masse relative de la portée. Les vipères sont très sédentaires. L'espace vital individuel des adultes, estimé sur des périodes de 2 à 9 ans, couvre au plus quelques milliers de mètres carrés, sans différence significative entre sexes. Les femelles gestantes, très thermophiles, se déplacent très peu. Les immatures se dispersent dans le milieu sur de faibles distances. Il ne semble pas y avoir de tendance à l'émigration. Le taux d'accroissement de la population, calculé à partir de 6 estimations d'effectifs, indique un déclin significatif de la population. Une analyse de viabilité a mis en évidence une probabilité d'extinction sur 40 ans d'environ 60%. Le taux d'accroissement est beaucoup plus sensible aux probabilités de survie qu'aux fécondités. Le temps nécessaire pour recouvrer l'effectif de 1985 à partir de celui de 1993 dépend largement de la survie adulte et des variations annuelles de la fécondité.
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Smedley, Todd Matthew. « The covenant theology of Zacharias Ursinus ». Thesis, University of the Highlands and Islands, 2012. https://pure.uhi.ac.uk/portal/en/studentthesis/the-covenant-theology-of-zacharias-ursinus(1dce61f1-ef90-40ff-b69b-065fd520ccf5).html.

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This thesis provides an analysis of the covenant thought of Zacharias Ursinus (1534- 1583) who further advanced the idea of a bi-covenantal scheme in the development of covenant theology in the sixteenth century and seeks to demonstrate how such advancement did not diminish the gratuitous nature of the gospel. Understood within the larger framework of his theological system it becomes evident that his original foedus naturale did not arise out of an overly speculative scholastic methodology. Instead, it served as the corollary of the foedus gratiae he inherited from his Reformed predecessors. An analysis of his teaching on the natural law, the law-gospel dichotomy, the federal headship of Adam and Christ and the imputation of Christ’s righteousness for Adam’s disobedience reveals how the foedus naturale emerged organically from his convictions on these heads of doctrine. The methodology is both systematic and historical. It begins with a study of his theological development as examined in the context of his life and written works followed by a review of the contributions of previous secondary literature that exists on this subject. Both the doctrine of God and the doctrine of the knowledge of God are analyzed as they provide insight into his theological methodology showing it to be biblical rather than philosophically speculative. The heart of the thesis is a close examination of the foedus gratiae and the foedus naturale which demonstrates how the two complement each other and how they relate to other theological distinctives within his thought. The study concludes by showing how his doctrine of justification, namely double imputation, lays the basis for the formulation of his pioneering idea of a foedus naturale.
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Napier, James Alexander. « Variation and adaptation in Allium ursinum L ». Thesis, University of Ulster, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242062.

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Oechsle, Ursina [Verfasser], et Klaus [Akademischer Betreuer] Spindler. « Untersuchung der Nukleation an Wärmeübertrageroberflächen in einem Eisspeicher / Ursina Oechsle ; Betreuer : Klaus Spindler ». Stuttgart : Universitätsbibliothek der Universität Stuttgart, 2020. http://d-nb.info/1216107378/34.

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Echeverría-Lozano, Guillermina. « Conflict management in wild chacma baboons (Papio cynocephalus ursinus) ». Thesis, University of Liverpool, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.414832.

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Skerratt, Lee Francis. « Sarcoptic mange in the common wombat, Vombatus ursinus (Shaw, 1800) ». Connect to thesis, 2001. http://eprints.unimelb.edu.au/archive/00000709.

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Keller, Oliver. « Paracotalpa ursina species complex revealed : the true biodiversity of the California bear scarabs (Coleoptera : Scarabaeidae) ». Thesis, Wichita State University, 2014. http://hdl.handle.net/10057/10966.

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Rahikainen, Marjatta. « N.R. af Ursin aatelismies Suomen työvänliikkeessä / ». Helsinki : Suomen historiallinen seura, 1986. http://catalogue.bnf.fr/ark:/12148/cb414438916.

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Sanfelice, Daniela. « Ontogenia craniana comparada de Arctocephalus australis, Callorhinus ursinus e Otaria byronia (Otariidae : Pinnipedia) ». reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2003. http://hdl.handle.net/10183/15623.

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The search for mechanisms that can generate major morphological changes has led to the study of ontogeny, in part because some kinds of modifications of ontogenies seem an excelent way to generate major phenotypic change. We focus here on Arctocephlaus australis, Callorhinus ursinus and Otaria byronia with the aim of contributing to the understanding of the origin, structure and temporal patterns of otarid morphological diversity. The pattern of change in shape during postnatal development in otarid skull was studied and described by geometric and traditional morphometrics. Our aims are: to compare the skull ontogeny of the species invocated in identifying and in describing shape alterations in the skull; to evaluate and to describe comparatively the sexual dimorphism and disparity during the ontogeny; to study the covariance between size and shape in relationship with age-groups; to investigate the changes in the ontogeny and their relationships with the evolution of the Otariidae Family; to analyze the conservation of ontogenetic trajectories over time, between sexes and among species; to characterize growth trajectories and to compare them among taxa with respect to isometry; to describe the parameters of growth and development of the focused species and to compare the two different approaches employed. Using traditional morphometrics, the allometry vectors for all species were significantly different from isometry. Dimorphism in the allometric vector is observed only in O. byonia and the difference between males and females of the fur seals are related with adult body size. The comparisons species/sex groups revealed similar vectors (any significant shape disassociation are verified in the inter-specific analyzes), suggesting lower plasticity of the ontogenies. Using geometrical methods, the dimorphism is more conspicuous in adult shapes but this is not true for the level of disparity between sexes of O. byronia. Although that dimorphism is linked with size this is not only a question of scaling or allometry (which is present in the morphogenesis of all species, especially in O. byronia). Additionally, the slopes of changes in shape related with size increase are different in A. australis and O. byronia, but are equal in C. ursinus, which is the smaller species. We suggest post-displacement as one of the factors that could have acted in the origin of the sexual dimorphism in the skull of C. ursinus. Heterochrony, perhaps is present in the roots of the modifications suffered by the ontogeny of A. australis and O. byronia too, considering the differences in the rates of development between the sexes of both species (and overall in O. byronia), but surely repatterning allometric is involved too in these cases. We verified that ontogenies can not be summarized by a single linear vector in any analyzed group, where C. ursinus ontogeny is the more linear and O. byronia the more multi-dimensional species among the 3 that we had examined. Shape changes in the otarids studied here are more related with size than with age and any of the species share a common growth allometry or a common ontogenetic trajectory/pattern. In the same way, shapes at onset or offset are not the same in any case. When the three species are pooled together, initial shapes are always very different among the species and the distances between shapes increase with time almost independently from size. On the other hand, when the complete samples are considered, all the ontogenetic trajectories are significantly different in the directions of the allometric vectors during ontogeny. Ontogenetic trajectories differ significantly among almost all the pairs compared, except for the trajectories of A. australis and C. ursinus males. They are no more different than expected by chance considering the range of angles within each sample. A similar pattern is found when the subadults are compared between pairs of species and when we compare adult males of A. australis with adult males of O. byronia. The juveniles are no more different than expected by chance (correlation between ontogenies in that phase is equal to one), excepti between C. ursinus and O. byronia. The ontogenetic trajectory of C. ursinus is the shorter and of O. byronia is the longer being almost three times longer than the former. A. australis has an intermediary length of ontogenetic trajectory. For the sample comprising all three species disparity increase significantly over ontogeny since the disparity of the adults is near the two times of the disparity between juveniles. For any ontogenetic stage, O. byronia is the species that contributes for the disparity of the all group, followed by C. ursinus. When we consider the three species together, the pattern of disparity do not change a lot during ontogeny. Ontogenies examined herein are clearly not constrained and perhaps the differences in patterns have additive effects in the differentiation of the ontogenies. Whether ontogenetic trajectories are linear or curve could be a function of developmental timing or more specifically it could depend on the age at which allometries stabilize in post-natal ontogenies. Otherwise, the amount of differences between species in the ontogenies is in agreement with the phylogenetic relationships. Finally, we addressed basically the following questions: Is onset time the same in the species? Is offset time the same in these species? Does growth rate differ between the species. The answer to those questions could be summarized by the conclusion. but we conclude that the changes in otarids skull ontogenies had occurred in spatial and temporal terms.
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Livres sur le sujet "Ursinia"

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Vinzens, Ursina. Ursina Vinzens. Chur : Edition Galerie Giacometti, 1991.

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Schmidt, Yvonne. MIMOS 2017 : Ursina Lardi. Bern : Peter Lang International Academic Publishers, 2017.

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Hasdeu, B. P. Ursita. București : Editura Gramar, 1994.

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Yost, Calvin Daniel. Ursinus College : A history of its first hundred years. Collegeville, PA : The College, 1985.

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Jaslovský, Marian. Dežo Ursiny : Pevniny a vrchy. Bratislava : Médiá, 1997.

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Jaslovský, Marian. Dežo Ursiny : Pevniny a vrchy. 3e éd. Bratislava : Slovart, 2011.

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Gavidia, Francisco. Ursino : Drama en cinco actos. San Salvador, El Salvador : Norma, 1996.

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Gavidia, Francisco. Ursino : Drama en cinco actos. San Salvador, El Salvador : Norma, 1996.

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Napier, James Alexander. Variation and adaptation in allium ursinum L.. [S.l : The Author], 1994.

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Wiśniewska, Halina. Język polski w łacińskich pracach Jana Ursinusa. Lublin : Wydawn. Uniwersytetu Marii Curie-Skłodowskiej, 1998.

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Chapitres de livres sur le sujet "Ursinia"

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Azimova, Shakhnoza S., et Anna I. Glushenkova. « Ursinia calenduliflora Benth. et Hook. f. » Dans Lipids, Lipophilic Components and Essential Oils from Plant Sources, 141. London : Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-323-7_461.

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Lim, T. K. « Rubus ursinus x idaeus ‘Boysenberry’ ». Dans Edible Medicinal And Non-Medicinal Plants, 581–86. Dordrecht : Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4053-2_67.

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De Spirito, Giuseppe. « Ursino Ε Damaso - Una Νοτα ». Dans Peregrina Curiositas, 263–74. Göttingen : Vandenhoeck & Ruprecht, 1994. http://dx.doi.org/10.13109/9783666539299.263.

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Bierma, Lyle D. « Ursinus and the Theological Landscape of the Heidelberg Catechism ». Dans The Spirituality of the Heidelberg Catechism, 9–24. Göttingen : Vandenhoeck & Ruprecht, 2015. http://dx.doi.org/10.13109/9783666550843.9.

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Kiyota, Masashi. « Site Fidelity, Male Harassment and Female Gregariousness : Factors Shaping the Highly Polygynous Mating System of the Northern Fur Seal (Callorhinus ursinus (C. ursinus)) ». Dans Ethology and Behavioral Ecology of Otariids and the Odobenid, 161–82. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-59184-7_8.

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Rietz, B., H. Isensee, H. Strobach, S. Makdessi et R. Jacob. « Cardioprotective Actions of Wild Garlic (Allium Ursinum) in Ischemia and Reperfusion ». Dans Cellular Function and Metabolism, 143–50. Boston, MA : Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3078-7_20.

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Mass, Alla M. « Retinal Topography in the Walrus (Odobenus Rosmarus Divergence) and Fur Seal (Callorhinus Ursinus) ». Dans Marine Mammal Sensory Systems, 119–35. Boston, MA : Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3406-8_7.

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Fayvush, George, Alla Aleksanyan, Naiba Mehdiyeva, Valida Alizade, Ketevan Batsatsashvili, Zaal Kikvidze, Manana Khutsishvili et al. « Allium paradoxum (M. Bieb.) G. Don Allium ursinum L. Allium victorialis L. Amaryllidaceae ». Dans European Ethnobotany, 1–7. Cham : Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-50009-6_135-1.

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Fayvush, George, Alla Aleksanyan, Naiba P. Mehdiyeva, Valida M. Alizade, Ketevan Batsatsashvili, Zaal Kikvidze, Manana Khutsishvili et al. « Allium paradoxum (M. Bieb.) G. Don Allium ursinum L. Allium victorialis L. Amaryllidaceae ». Dans European Ethnobotany, 99–105. Cham : Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49412-8_135.

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Goulet, Anne-Madeleine. « The Princesse des Ursins, Loyal Subject of the King of France and Foreign Princess in Rome ». Dans Music and Diplomacy from the Early Modern Era to the Present, 191–207. New York : Palgrave Macmillan US, 2014. http://dx.doi.org/10.1057/9781137463272_10.

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Actes de conférences sur le sujet "Ursinia"

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Sorescu, Ana �. Alexandra, Alexandrina Nuta et Rodica �. Mariana Ion. « ALLIUM URSINUM - MEDIATED ONE POT GREEN SYNTHESIS OF SILVER NANOPARTICLES : KINETICS AND DEGRADATION OF AZO � DYES ». Dans 20th International Multidisciplinary Scientific GeoConference Proceedings SGEM 2020. STEF92 Technology, 2020. http://dx.doi.org/10.5593/sgem2020/5.1/s20.006.

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Kornev, S. I., V. S. Nikulin et O. A. Belonovich. « Number of northern fur seals (Callorhinus ursinus) at the rookeries of Bering Island in 2013–2017 ». Dans Marine mammals of the Holarctic. Marine Mammal Council, 2019. http://dx.doi.org/10.35267/978-5-9904294-0-6-2019-1-137-145.

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Rapports d'organisations sur le sujet "Ursinia"

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Kucklick, John, Jessica Reiner, Michele Schantz, Jennifer Keller, Jennifer Hoguet, Catherine Rimmer, Tamika Ragland et al. persistent organic pollutants and vitamins in northern fur seals (callorhinus ursinus) collected from St. Paul Island, Alaska as part of the Alaska Marine Mammal Tissue Archival Project. Gaithersburg, MD : National Institute of Standards and Technology, 2013. http://dx.doi.org/10.6028/nist.ir.7958.

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Geologic map of the Ursine-Panaca Summit-Deer Lodge area, Lincoln County, Nevada and Iron County, Utah. US Geological Survey, 1997. http://dx.doi.org/10.3133/i2479.

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