Academic literature on the topic 'Pasture plant diversity'
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Journal articles on the topic "Pasture plant diversity"
Cripps, M. G., M. R. McNeill, H. Patrick, B. Wiseman, F. Nobilly, and G. R. Edwards. "Invertebrate abundance and diversity in intensively managed dairy pastures." New Zealand Plant Protection 65 (January 8, 2012): 295. http://dx.doi.org/10.30843/nzpp.2012.65.5411.
Full textSanderson, M. A., S. C. Goslee, K. J. Soder, R. H. Skinner, B. F. Tracy, and A. Deak. "Plant species diversity, ecosystem function, and pasture Management—A perspective." Canadian Journal of Plant Science 87, no. 3 (July 1, 2007): 479–87. http://dx.doi.org/10.4141/p06-135.
Full textSnow, V. O., P. N. Smale, and M. B. Dodd. "Process-based modelling to understand the impact of ryegrass diversity on production and leaching from grazed grass-clover dairy pastures." Crop and Pasture Science 64, no. 10 (2013): 1020. http://dx.doi.org/10.1071/cp13263.
Full textReed, Kinsey, and Ember M. Morrissey. "Bridging Ecology and Agronomy to Foster Diverse Pastures and Healthy Soils." Agronomy 12, no. 8 (August 12, 2022): 1893. http://dx.doi.org/10.3390/agronomy12081893.
Full textMaze, Jack, and Roy Turkington. "The influence of pasture age, plant density, and genotype on intraspecific diversity of Trifolium repens (white clover)." Canadian Journal of Botany 74, no. 7 (July 1, 1996): 1189–92. http://dx.doi.org/10.1139/b96-142.
Full textKaur, Kamaljit, David J. Midmore, Rajesh K. Jalota, and Nanjappa Ashwath. "Pasture composition in cleared and uncleared woodlands." Australian Journal of Botany 54, no. 5 (2006): 459. http://dx.doi.org/10.1071/bt05174.
Full textTamahina, Aida, and Urfa Turan Ogly Turabov. "Production potential of the Kabardino-Balkarian Republic pasture ecosystems." E3S Web of Conferences 262 (2021): 03023. http://dx.doi.org/10.1051/e3sconf/202126203023.
Full textDavis, RD, RM Boland, and AT Lisle. "The developing relationship between Stylosanthes and anthracnose after 14 years in a North Queensland pasture. 3. Diversity in the plant population." Australian Journal of Experimental Agriculture 34, no. 5 (1994): 627. http://dx.doi.org/10.1071/ea9940627.
Full textZehnder, Tobias, Andreas Lüscher, Carmen Ritzmann, Caren M. Pauler, Joel Berard, Michael Kreuzer, and Manuel K. Schneider. "Dominant shrub species are a strong predictor of plant species diversity along subalpine pasture-shrub transects." Alpine Botany 130, no. 2 (September 14, 2020): 141–56. http://dx.doi.org/10.1007/s00035-020-00241-8.
Full textGerard, Philippa J., Derrick J. Wilson, and Anastazia L. Docherty. "Does pasture plant diversity influence abundance and diversity of lacewings and Hymenopteran parasitoids?" New Zealand Plant Protection 71 (July 29, 2018): 207–13. http://dx.doi.org/10.30843/nzpp.2018.71.185.
Full textDissertations / Theses on the topic "Pasture plant diversity"
Trytsman, Marike. "Diversity and pasture potential of legumes indigenous to southern Africa." Thesis, University of Pretoria, 2013. http://hdl.handle.net/2263/40213.
Full textThesis (PhD)--University of Pretoria, 2013.
gm2014
Plant Science
unrestricted
Sangha, Kamaljit Kaur, and Kamaljit kaur@jcu edu au. "Evaluation of the effects of tree clearing over time on soil properties, pasture composition and productivity." Central Queensland University. School of Biological and Environmental Sciences, 2003. http://library-resources.cqu.edu.au./thesis/adt-QCQU/public/adt-QCQU20060921.115258.
Full textDufour, Alexia. "Multiscale assessment of plant diversity in wooded pastures of the jura mountains." Besançon, 2006. http://www.theses.fr/2006BESA2059.
Full textThe world-wide loss of biodiversity at all scales has become a matter of urgent concern, and improving our understanding of local drivers of biodiversity in natural and anthropogenic ecosystems is now crucial for conservation. The main objective of this study was to further our comprehension of the driving forces controlling biodiversity patterns in a complex and diverse ecosystem of high conservation value, wooded pastures. We tested several hypotheses relating spatial pattern scale and biodiversity and explored spatial patterns of biodiversity in a multi-scale context and using different measures of biodiversity (species richness and composition), with field data. Data were collected using an innovative hierarchical sampling design and combined with remotely-sensed lidar data. Their analysis using recent statistical tools showed that: - species richness generally increased with environmental heterogeneity. - the spatial structure of plant species composition was related to topography at the coarsest scales and insolation at finer scales. The non-environmental fraction of the spatial variation in species composition had a complex relationship with several species traits, suggesting a scale-dependent link to biological processes. - the pairwise relationships between alpha, beta and gamma diversity were strongly scale-dependent and did not follow the expected patterns, at least at certain scales. Thus, our results highlight the crucial role of spatial structure for all components of biodiversity. They also emphasize the importance of considering multiple spatial scales and multiple scale components when studying species diversity
Silva, Anderson de Carvalho. "Caracteriza??o agron?mica, molecular e fitoqu?mica de Eplingiella Harley & J.F.B. Pastore." Universidade Estadual de Feira de Santana, 2015. http://localhost:8080/tede/handle/tede/293.
Full textMade available in DSpace on 2016-01-26T21:56:33Z (GMT). No. of bitstreams: 1 TESE_Anderson_FINAL.pdf: 3427530 bytes, checksum: 027d12f66415d71dc327e860609665fe (MD5) Previous issue date: 2015-06-29
Conselho Nacional de Pesquisa e Desenvolvimento Cient?fico e Tecnol?gico - CNPq
Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES
Funda??o de Amparo ? Pesquisa do Estado da Bahia - FAPEB
Eplingiella fruticosa (Salzm. Ex Benth.) Harley & JFB Pastore is an aromatic species, native, occurring in six states in northeastern Brazil (Bahia, Sergipe, Pernambuco, Paraiba, Rio Grande do Norte and Cear?). Popularly known as "alecrim de vaqueiro", is commonly found in street markets of the region and used to combat pain and seizures. Reviews in mice and in vitro studies show analgesic activity, vasodilating, cardioprotetiva, anti-inflammatory and larvicidal of its essential oil and of different types of the leaves extract. Recent studies show great variability in essential oil chemical composition of E. fruticosa, related to soil and climatic conditions and different plant organs. Thus, the species has great potential for exploration both agronomic, and by pharmaceutical companies. The aim of this study was to evaluate the vegetative propagation capacity and characterize previously Eplingiella genotypes, through morphological, agronomic, phytochemicals and molecular data. In Chapter I, two experiments were conducted: the first tested the effect of three substrates and the second evaluated five concentrations of IBA and three periods of cultivation. The design was a randomized block design with four replications. We evaluated survival percentage (% S), percentage of rooted cuttings (% EE), root length (CRE), number of shoots (NBE), dry mass of leaves (MSF), root dry weight (MSR) and total dry matter (MST). In Chapter II, twelve genotypes were collected, propagated vegetatively and transplanted. Twelve months after transplantation were assessed 12 quantitative traits, eight morphological and agronomic four. In Chapter III, the total DNA was extracted, then 20 primers were tested, of which nine were selected because they have better electrophoretic profiles agarose gel (2%). The binary matrix was computed in GEOCOMPAR II. It is estimated the diversity of the genetic structure parameters and the data were subjected to Bayesian analysis, and Neighbor-joining dendrogram and principal component analysis (PCA) based on matrix of Nei distances. And in Chapter IV, samples of 100g of leaves each repetition per genotype were used in the essential oil hydrodistillation in Clevenger type apparatus for three hours, quantifying the content. The identification of the compounds and their contents was performed by GC (FID) and GC / MS data 15 and the major compounds were used in diversity analysis. They have been made to cluster analysis and canonical variables, using as dissimilarity measure the Mahalanobis distance (D2). In the first experiment of Chapter I, significant differences were found for CRE, NBE, MSF, MSR and MST, with the best performance for the commercial substrate. In the second, positive effects have been identified both the addition of AIB as the cultivation time on the CRE variables, NBE, MSF and MSR, reaching maximum increment to the estimated concentration of 1.5 g L-1, at 60 days of cultivation. In Chapter II, there was significant variation by F test (p <0.01) for the CF features, LF, CBD, CBE, LP, and MFF MSF. The genotypes formed two groups for almost all variables, by Scott-Knott test (p <005), except for LP, which formed three. The EF002 and EF003 genotypes presented the highest levels for almost all variables. There was the formation of three groups for both UPGMA and for the canonical variables (CV). The characteristics that most contributed to the formation of groups were CBE, MFF and CF. The genotypes EF002, EF003, EF005 and EF012 stood out because they have higher genetic distances. In CHAPTER III, primers produced 131 polymorphic bands. The diversity index of Nei (Ne) ranged between 0.31 and 0.39, while Shannon (I) ranged between 0.33 and 0.48. The percentage coefficient of genetic differentiation (Gst) was 0.29. In AMOVA most of the variation was within populations (69%), while among populations was 27% and 4% among species, indicating a good genetic structure. The average value of Fst was 0.175, demonstrating intermediate differentiation between populations. The structure of the Bayesian analysis method revealed three possibilities for the formation of groups (K = 2; = 6; 8 =;), however, it presented many migrants and high level of mixing individuals. The dendrogram generated by the Neighbor-Joining method confirmed the formation of two groups, with good support for major clades (100%). PCA analysis in the first two axis explained 21.06% of the total variation among populations. Finally, in Chapter IV, the genotypes were classified into four clusters: 1 - EF001 genotypes, EF006, EF007, EF008, EF010, EF011 and EF012 with E-caryophyllene and bicyclogermacrene as major; 2 - EF002 and EF003 genotypes, with the majority same as the previous group, however, percentage with average about 30% higher; 3 - EF004 and EF005 genotypes that showed a greater production of E-caryophyllene; and 4 - with EF009 genotype, forming a single group to present ?-pinene as balanced majority and percentage among the rest. This result was confirmed by canonical variables, which explained 76% of the variation. The bicyclogermacrene compounds, 1,8-cineol, ?-copaene and spathulenol represented the most important variables for analysis.
Eplingiella fruticosa (Salzm. ex Benth.) Harley & J.F.B. Pastore ? uma esp?cie arom?tica, nativa, que ocorre em seis estados do nordeste brasileiro (Bahia, Sergipe, Pernambuco, Para?ba, Rio Grande do Norte e Cear?). Popularmente conhecida como ?alecrim de vaqueiro?, ? comumente encontrada em feiras livres da regi?o e utilizada no combate a dores e convuls?es. Avalia??es em camundongos e in vitro comprovam atividades analg?sicas, vasodilatadora, cardioprotetiva, antinflamat?ria e larvicida do seu ?leo essencial e de diferentes tipos de extrato de suas folhas. Estudos recentes apontam grande variabilidade na composi??o qu?mica do ?leo essencial de E. fruticosa, relacionada ?s condi??es edafoclim?ticas e aos diferentes ?rg?os vegetais. Sendo assim, a esp?cie apresenta grande pot?ncial de explora??o tanto agron?mica, quanto por ind?strias farmac?uticas. O objetivo geral deste estudo foi avaliar a capacidade de propaga??o vegetativa e caracterizar, previamente, gen?tipos de E. fruticosa, por meio de dados morfol?gicos, agron?micos, fitoqu?micos e moleculares. No CAP?TULO I, foram conduzidos dois experimentos: o primeiro testou o efeito de tr?s substratos e o segundo avaliou cinco concentra??es de AIB e tr?s per?odos de cultivo. O delineamento foi em blocos casualizado, com quatro repeti??es. Avaliou-se percentagem de sobreviv?ncia (%S), percentagem de estacas enraizadas (%EE), comprimento da raiz (CRE), n?mero de brota??es (NBE), massa seca de folhas (MSF), massa seca de raiz (MSR) e massa seca total (MST). No CAP?TULO II, doze gen?tipos foram coletados, propagados vegetativamente e transplantados. Doze meses ap?s o transplante foram avaliadas 12 caracter?sticas quantitativas, sendo oito morfol?gicase quatro agron?micas. No CAP?TULO III, o DNA total foi extra?do, em seguida 20 iniciadores foram testados, dos quais nove foram selecionados por apresentarem melhores perfis eletrofor?ticos em gel de agarose (2%). A matriz bin?ria foi computada no GEOCOMPAR II. Estimou-se os par?metros de diversidadee a estrutura gen?tica os dados foram submetidos ? an?lise Bayesiana, al?m de dendrograma Neighbor-joining e an?lise de componentes principais (PCA) com base na matriz de dist?ncias de Nei. E no CAP?TULO IV, amostras de 100g de folhas de cada repeti??o por gen?tipo foram utilizadas na hidrodestila??o do ?leo essencial, em aparelho tipo clevenger, durante tr?s horas, quantificando-se o teor. A identifica??o dos compostos e seus teores foi realizada por CG (DIC) e CG/EM e os dados de 15 compostos majorit?rios foram utilizados nas an?lises de diversidade. Foram procedidas an?lise de agrupamento e de vari?veis can?nicas, utilizando como medida de dissimilaridade a dist?ncia generalizada de Mahalanobis (D2).No primeiro experimento do CAP?TULO I, foram verificadas diferen?as significativas para CRE, NBE, MSF, MSR e MST, com melhor desempenho para o substrato comercial. No segundo, foram identificados efeitos positivos tanto da adi??o de AIB quanto dos tempos de cultivo sobre as vari?veis CRE, NBE, MSF e MSR, atingindo incremento m?ximo com a concentra??o estimada de 1,5 g L-1, aos 60 dias de cultivo. No CAP?TULO II, houve varia??o significativa, pelo teste de F (p<0,01), para as caracter?sticas CF, LF, CBD, CBE, LP, MFF e MSF. Os gen?tipos formaram dois grupos para quase todas as vari?veis, pelo teste de Scott-Knott (p<005), exceto para LP, que formou tr?s. Os gen?tipos EF002 e EF003 apresentaram as maiores m?dias para quase todas vari?veis. Houve a forma??o de tr?s grupos, tanto para UPGMA quanto para as vari?veis can?nicas (VC). As caracter?sticas que mais contribu?ram para a forma??o dos grupos foram CBE, MFF e CF. Os gen?tipos EF002, EF003, EF005 e EF012 se destacaram por apresentarem maiores dist?ncias gen?ticas. No CAP?TULO III, os iniciadores produziram 131 bandas polim?rficas. O ?ndice de diversidade de Nei (Ne) variou entre 0,31 e 0,39, enquanto Shannon (I) variou entre 0,33 e 0,48. O percentual do coeficiente de diferencia??o gen?tica (Gst) foi de 0,29. Na AMOVA a maior parte da varia??o ficou dentro das popula??es (69%), enquanto entre popula??es foi de 27% e entre esp?cies de 4%, indicando uma boa estrutura??o gen?tica. O valor m?dio de Fst foi 0,175, demonstrando diferencia??o intermedi?ria entre as popula??es. As an?lises de estrutura pelo m?todo Bayesiano revelou tr?s possibilidades de forma??o de grupos (K=2;=6;=8;), no entanto, apresentou muitos indiv?duos migrantes e elevado n?vel de miscigena??o. O dendograma gerado pelo m?todo de Neighbor-Joining confirmou a forma??o de dois grupos, com boa sustenta??o para os principais clados (100%). Na an?lise de PCA os dois primeiros axis explicaram 21,06% da varia??o total entre as popula??es. Por fim, no CAP?TULO IV, os gen?tipos foram classificados em quatro clusters: 1 - gen?tipos EF001, EF006, EF007, EF008, EF010, EF011 e EF012, com E-cariofileno e biciclogermacreno como majorit?rios; 2 - gen?tipos EF002 e EF003, com os mesmos majorit?rios que o grupo anterior, no entanto, com percentuais m?dios cerca de 30% superiores; 3 - gen?tipos EF004 e EF005, que evidenciaram uma maior produ??o de E-cariofileno; e 4 - com gen?tipo EF009, formando um grupo isolado por apresentar ?-pineno como majorit?rio e percentuais equilibrados entre os demais. Esse resultado foi confirmado pelas Vari?veis Can?nicas, que explicou 76% da varia??o. Os compostos biciclogermacreno, 1,8-cineol, ?-copaeno e espatulenol representaram as vari?veis de maior import?ncia para a an?lise.
Vazquez, Ana M. "Possible Drivers in Endophyte Diversity and Transmission in the Tomato Plant Bacterial Microbiome." The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1594918263597025.
Full textMabuza, Thembisile Veronicah. "Evaluating long term effects of fire frequency on soil seed bank composition and species diversity in a semi-arid , South African savanna." Thesis, University of Fort Hare, 2011. http://hdl.handle.net/10353/346.
Full textDebouk, Haifa. "Assessing the effect of global change on plant functional structure, greenhouse gases, and soil functions in grasslands." Doctoral thesis, Universitat de Lleida, 2017. http://hdl.handle.net/10803/436894.
Full textEl objetivo principal de esta tesis fue investigar el efecto de los grupos funcionales de plantas sobre la estabilidad de la vegetación, los flujos de GEI y las funciones del suelo, y cómo las condiciones climáticas regulan sus interacciones. La estructura funcional de las plantas en pastos influyó la estabilidad de la vegetación, los flujos de GEI, la actividad y fertilidad del suelo, y ese efecto está regulado por el clima. El calentamiento causó la dominancia de especies oportunistas sobre las más conservadoras; reduciendo así la riqueza específica. Los rasgos funcionales tuvieron una mayor influencia en la productividad y estabilidad de las comunidades frente al efecto de la diversidad. Los flujos de GEI aumentaron en verano y disminuyeron con la altitud. La interacción entre grupos funcionales incrementó la absorción de CH4 y N2O respecto a grupos individuales. Las interacciones entre grupos funcionales favorecieron también las funciones de suelo relacionadas con el ciclo de N.
The main objective of this thesis is to investigate how plant functional types (PFT) affect vegetation stability, greenhouse gas (GHG) fluxes and soil functions, and how these interactions are regulated by climatic conditions. We found that plant functional structure strongly influences vegetation stability, GHG fluxes, and soil activity and fertility in grassland, but this relationship is regulated by climate. Warming lead to the dominance of acquisitive fast growing species over conservative species; thus reducing species richness. The functional traits structure in grasslands had greater influence on the productivity and stability of the community under warming, compared to diversity effects. GHG fluxes decreased with altitude- the colder the grassland site the lower the fluxes-, and increased during summer. The interaction between PFTs enhanced CH4 and N2O uptake compared to single PFTs. Also, PFT evenness and pairwise interactions between PFTs enhanced soil functions related to the N cycle.
Pardo, Guereño Iker. "Distribution and dynamics of multiple components of plant diversity in a high mountain area: the Ordesa-Monte Perdido National Park = Distribución y dinámica temporal de los diferentes componentes de la diversidad vegetal en la alta montaña: el Parque Nacional de Ordesa y Monte Perdido." Doctoral thesis, Universitat de Barcelona, 2016. http://hdl.handle.net/10803/384840.
Full textEn esta tesis investigamos la distribución de los componentes taxónomico, filogenético y funcional de la diversidad vegetal en la alta montaña, y cómo ha respondido a los principales motores de cambio global en montañas (cambio climático y de uso de suelo) en las últimas décadas. Para abordar estas dos cuestiones usamos una aproximación a varias escalas, combinando información recopilada en bases de datos con datos descriptivos y experimentales obtenidos en campo, poniendo especial énfasis en mejorar los métodos analíticos de las aproximaciones utilizadas. Nuestra investigación se llevó a cabo en el Pirineo Central, especialmente en el Parque Nacional de Ordesa y Monte Perdido (PNOMP). En el primer capítulo examinamos el sesgo del esfuerzo de muestreo en una clásica base de datos de herbario, y cómo éste puede afectar a los análisis de los patrones de diversidad. Desarrollamos un método nuevo que permitió detectar diferencias importantes en la distribución del esfuerzo de muestreo a lo largo del PNOMP. Esta información fue usada en el segundo capítulo, donde demostramos por primera vez que, además de la riqueza específica, el patrón de distribución del resto de los componentes de la diversidad puede verse distorsionado por el sesgo de muestreo. Tras utilizar una base de datos elaborada a partir de inventarios de comunidades, observamos que los diferentes componentes de la diversidad presentaron una distribución distinta a lo largo del PNOMP. Este resultado demuestra que nuestra habilidad para identificar áreas prioritarias para la conservación a partir de bases de datos clásicas de diversidad es muy limitada. Los pastos resultaron ser el hábitat más rico en término de número de especies y endemismos, mientras que algunos tipos de bosques de hoja caduca fueron identificados como puntos calientes de historia evolutiva y funcional. En los siguientes capítulos examinamos la respuesta de las comunidades más ricas, los pastos de alta montaña, al descenso generalizado del pastoreo y el calentamiento climático. En el capítulo tercero analizamos los resultados de la revisita de transectos de vegetación situados en el ecotono del límite del bosque superior, muestreados 11 años antes. El escaso efecto del incremento de la cobertura arbórea sobre las comunidades pone de manifiesto la lenta respuesta de las comunidades alpinas a cambios estructurales del hábitat. En el cuarto capítulo examinamos la respuesta de los pastos alpinos a lo largo de dos décadas, tras revisitar una docena de parcelas permanentes distribuidas a lo largo de un gradiente altitudinal en dos valles del Pirineo Central. Tras considerar el error de muestreo y la fluctuación interanual de las comunidades, no observamos señales evidentes de cambios ni a nivel de comunidad ni de especies, ni tampoco un aumento de especies leñosas. Los grupos de especies con tendencias opuestas no mostraron rasgos funcionales significativamente diferentes, cuando fue considerada la abundancia y autocorrelación evolutiva de éstos. La gran inercia ecológica de los pastos alpinos fue también confirmada en un experimento de exclusión de herbivoría que duró 19 años (quinto capítulo), donde la riqueza de especies no mostró un efecto significativo en respuesta al tratamiento. La ausencia de ganado sólo resultó en una trayectoria divergente de la comunidad tras una década, y coincidiendo con un periodo excepcionalmente cálido y seco. Este resultado sugiere que el cese del pastoreo y el aumento de las temperaturas podrían tener un efecto aditivo sobre las comunidades vegetales. En conjunto, todos estos resultados ponen de manifiesto que las comunidades de pastos alpinos frente a los principales motores de cambio en montaña puede ser más lenta de lo que se esperaba según los modelos predictivos, la rápida sucesión ecológica (matorralización) observada en varios pastos subalpinos y montanos a lo largo del Pirineo, y los cambios en las comunidades de cumbres (termofliación) descritos en el propio PNOMP. La aparente estabilidad registrada en nuestro estudio podría revertir si se sobrepasan puntos de inflexión críticos. Sin embargo, la lenta dinámica aquí observada sugiere que no es tarde para tomar medidas de gestión para garantizar la conservación de estos pastos excepcionalmente ricos. El mantenimiento o restauración de las actividades del pastoreo tradicional se vislumbra como una solución simple y efectiva para paliar los efectos de los principales motores de cambio global sobre las comunidades alpinas.
(9832535), Kamaljit Sangha. "Evaluation of the effects of tree clearing over time on soil properties, pasture composition and productivity." Thesis, 2003. https://figshare.com/articles/thesis/Evaluation_of_the_effects_of_tree_clearing_over_time_on_soil_properties_pasture_composition_and_productivity/13422212.
Full text(9847298), Zongjian Yang. "Resource allocation within plants: Some theoretical and practical implications for control of plant development." Thesis, 2003. https://figshare.com/articles/thesis/Resource_allocation_within_plants_Some_theoretical_and_practical_implications_for_control_of_plant_development/13424417.
Full textBook chapters on the topic "Pasture plant diversity"
Street, Kenneth A., Larry D. Robertson, and Nigel Maxted. "Utilisation of Forage and Pasture Legume Diversity." In Plant Genetic Resources of Legumes in the Mediterranean, 327–53. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-9823-1_18.
Full textFujita, Noboru, and Erdenegerel Ariunbold. "Plant Diversity and Productivity of Mongolian Nomadic Pasture in Relation to Land Use." In Social-Ecological Systems in Transition, 71–87. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54910-9_4.
Full textFujita, Noboru, Narantsetsegiin Amartuvshin, and Erdenegerel Ariunbold. "Annual Production and Species Diversity of Mongolian Pasture Plants in Relation to Grazing Pressure by Livestock." In The Mongolian Ecosystem Network, 131–43. Tokyo: Springer Japan, 2012. http://dx.doi.org/10.1007/978-4-431-54052-6_11.
Full textChanga, Taity, Jane Asiyo Okalebo, and Shaokun Wang. "Spatio-Temporal Dynamics of Soil Microbial Communities in a Pasture: A Case Study of Bromus inermis Pasture in Eastern Nebraska." In Agrometeorology [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.93548.
Full textMayer, Andrea C., Christine Huovinen, Veronika Stöckli, and Michael Kreuzer. "Plant Species Diversity, Forest Structure, and Tree Regeneration in Subalpine Wood Pastures." In Land Use Change and Mountain Biodiversity, 249–60. CRC Press, 2006. http://dx.doi.org/10.1201/9781420002874-18.
Full textKreuzer, Michael, Andrea Mayer, Christine Huovinen, and Veronika Stoeckli. "Plant Species Diversity, Forest Structure, and Tree Regeneration in Subalpine Wood Pastures." In Land Use Change and Mountain Biodiversity, 249–59. CRC Press, 2006. http://dx.doi.org/10.1201/9781420002874.ch18.
Full textYoung, Kenneth R. "Environmental and Social Consequences of Coca/Cocaine in Peru: Policy Alternatives and a Research Agenda." In Dangerous Harvest. Oxford University Press, 2004. http://dx.doi.org/10.1093/oso/9780195143201.003.0019.
Full textReports on the topic "Pasture plant diversity"
Leis, Sherry, and Lloyd Morrison. Plant community trends at Tallgrass Prairie National Preserve: 1998–2018. National Park Service, October 2022. http://dx.doi.org/10.36967/2294512.
Full text