Gotowa bibliografia na temat „Floral resources”
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Artykuły w czasopismach na temat "Floral resources"
Melin, Annalie, Mathieu Rouget, Jonathan F. Colville, Jeremy J. Midgley i John S. Donaldson. "Assessing the role of dispersed floral resources for managed bees in providing supporting ecosystem services for crop pollination". PeerJ 6 (27.09.2018): e5654. http://dx.doi.org/10.7717/peerj.5654.
Pełny tekst źródłaPhillips, Benjamin B., Rosalind F. Shaw, Matthew J. Holland, Ellen L. Fry, Richard D. Bardgett, James M. Bullock i Juliet L. Osborne. "Drought reduces floral resources for pollinators". Global Change Biology 24, nr 7 (13.04.2018): 3226–35. http://dx.doi.org/10.1111/gcb.14130.
Pełny tekst źródłaJunker, Robert R., i Nico Blüthgen. "Dependency on floral resources determines the animals’ responses to floral scents". Plant Signaling & Behavior 5, nr 8 (sierpień 2010): 1014–16. http://dx.doi.org/10.4161/psb.5.8.12289.
Pełny tekst źródłaFoucher, Fabrice, Michel Chevalier, Christophe Corre, Vanessa Soufflet-Freslon, Fabrice Legeai i Laurence Hibrand-Saint Oyant. "New resources for studying the rose flowering process". Genome 51, nr 10 (październik 2008): 827–37. http://dx.doi.org/10.1139/g08-067.
Pełny tekst źródłaFairhurst, Stacey M., Lorna J. Cole, Tereza Kocarkova, Catherine Jones-Morris, Andy Evans i Gail Jackson. "Agronomic Traits in Oilseed Rape (Brassica napus) Can Predict Foraging Resources for Insect Pollinators". Agronomy 11, nr 3 (27.02.2021): 440. http://dx.doi.org/10.3390/agronomy11030440.
Pełny tekst źródłaQuirino, ZGM, i IC Machado. "Pollination syndromes in a Caatinga plant community in northeastern Brazil: seasonal availability of floral resources in different plant growth habits". Brazilian Journal of Biology 74, nr 1 (luty 2014): 62–71. http://dx.doi.org/10.1590/1519-6984.17212.
Pełny tekst źródłaRamalho, M., A. Kleinert-Giovannini i V. L. Imperatriz-Fonseca. "Utilization of floral resources by species of Melipona (Apidae, Meliponinae): floral preferences". Apidologie 20, nr 3 (1989): 185–95. http://dx.doi.org/10.1051/apido:19890301.
Pełny tekst źródłaReal, Leslie, i Beverly J. Rathcke. "Patterns of Individual Variability in Floral Resources". Ecology 69, nr 3 (czerwiec 1988): 728–35. http://dx.doi.org/10.2307/1941021.
Pełny tekst źródłaAndersson, Stefan. "Experimental demonstration of floral allocation costs in Crepis tectorum". Canadian Journal of Botany 84, nr 6 (czerwiec 2006): 904–9. http://dx.doi.org/10.1139/b06-041.
Pełny tekst źródłaRodrigues, LC, i M. Rodrigues. "Floral resources and habitat affect the composition of hummingbirds at the local scale in tropical mountaintops". Brazilian Journal of Biology 75, nr 1 (marzec 2015): 39–48. http://dx.doi.org/10.1590/1519-6984.06913.
Pełny tekst źródłaRozprawy doktorskie na temat "Floral resources"
Antonsen, Adrienne Kendra. "Spatiotemporal Dynamics of Butterflies and Their Floral Resources". Thesis, North Dakota State University, 2020. https://hdl.handle.net/10365/31830.
Pełny tekst źródłaFultz, Jessica Erin. "Effects of shelterwood management on flower-visiting insects and their floral resources". Thesis, Montana State University, 2005. http://etd.lib.montana.edu/etd/2005/fultz/FultzJ0805.pdf.
Pełny tekst źródłaLarsson, Magnus. "To Bee or Not to Be : Critical Floral Resources of Wild-Bees". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Universitetsbiblioteket [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7108.
Pełny tekst źródłaGuezen, Jessica. "Past Floral Resources as a Predictor of Present Bee Visits in Agroecosystems". Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/37051.
Pełny tekst źródłaCoelho, Aline Goes. "A comunidade de plantas utilizada por beija-flores no sub-bosque de um fragmento de Mata Atl?ntica da Bahia, Brasil". Universidade Estadual de Feira de Santana, 2013. http://localhost:8080/tede/handle/tede/174.
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Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES
Studies on hummingbird/plant interactions in the Atlantic Forest have been providing major data on ornithophilous plants and on the role of these birds as pollen vectors and maintainers of plant communities. The aim of this study was to investigate a plant community used by hummingbirds, in order to recognize flowering phenological patterns and to identify pollen loads transported by visiting trochilidae. Fieldwork was performed from April 2009 to August 2011 in the understory of an Atlantic Forest area within Michelin Ecological Reserve, in Igrapi?na municipality, Bahia State. We identified hummingbirds from focal observations in flowering plants, recording their foraging strategies and the local of pollen deposition in their bodies. Data on morphology and floral biology were recorded for plants visited by hummingbirds, such as the number of flowers and buds monthly produced and if the plant was ornithophilous or not. Pollen attached to the beak, head, throat and chest of captured hummingbirds was removed, identified and counted in laboratory. About 18 plant species, most of them ornithophilous (83%), were visited by 13 hummingbird species, with Phaethornis ruber being the most frequent pollen vector. The plant community showed a continuous flowering, with sequential flowering peaks during the studied period. Sixteen pollen types and eight hummingbird species were recorded, with the beak being the main area for pollen deposition (58%), followed by the head (30%), throat (11%) and chest (1%). Differences on the local of pollen deposition on birds reduce the chance of mixing pollen from different species, allowing their coexistence by the sharing of the same pollen vector. Continuous flowering within the plant community assure the presence of their pollinators in the area, avoiding population dislocation towards floral resources. A high investment on floral morphology specialization allows a great deposition of pollen grains over a safe place on the body of the hummingbirds, maximizing plant reproductive success.
Os estudos sobre intera??es planta/beija-flor em Mata Atl?ntica t?m fornecido informa??es importantes sobre plantas ornit?filas e o uso de beija-flores como vetores de p?len e o papel destas aves na manuten??o de comunidades vegetais. O objetivo deste estudo foi investigar a comunidade vegetal utilizada por beija-flores, conhecer o padr?o fenol?gico de flora??o da comunidade al?m de identificar a carga pol?nica transportada pelos troquil?deos visitantes. O estudo foi realizado de abril de 2009 a agosto de 2011, no sub-bosque de uma ?rea de Mata Atl?ntica na Reserva Ecol?gica da Michelin, Igrapi?na, Bahia. Os beija-flores foram identificados a partir de observa??es focais em plantas floridas, registrando suas estrat?gias de forrageio e o local de deposi??o de p?len no corpo das aves. Das plantas visitadas pelos beija-flores, foram registrados dados sobre morfologia e biologia floral, sendo classificadas como ornit?fila ou n?o ornit?fila, e o n?mero de flores e bot?es produzidos mensalmente. Dos beija-flores capturados, foi removido o p?len impregnado em seu bico, cabe?a, garganta e peito. Os tipos pol?nicos foram identificados e contabilizados em laborat?rio. Foram registradas dezoito esp?cies de plantas, a maioria ornit?fila (83%), sendo visitadas por beija-flores. Treze esp?cies de beija-flores visitaram as plantas, sendo Phaethornis ruber o vetor de p?len mais frequente. Durante o per?odo de estudo, a comunidade vegetal apresentou flora??o cont?nua com picos de flora??o sequenciais. Dezesseis tipos pol?nicos foram identificados em oito esp?cies de beija-flores capturadas, sendo o bico o principal local de deposi??o de p?len (58%), seguido da cabe?a (30%), garganta (11%) e peito (1%). Diverg?ncias no local de deposi??o de p?len no corpo das aves reduz a probabilidade de mistura de p?len heteroespec?fico, permitindo a coexist?ncia de plantas que se beneficiam da partilha de polinizadores. A flora??o cont?nua da comunidade garante a presen?a de seus polinizadores na ?rea, evitando deslocamentos populacionais em busca de recurso. O alto investimento na morfologia floral especializada proporciona a deposi??o de grande quantidade de gr?os de p?len em local seguro do corpo da ave, maximizando o sucesso reprodutivo vegetal.
Cutter, Jasmine Antonia Villamarin. "Effect of Livestock Species on Floral Resources and Pollinators in Low-Diversity Grasslands". Thesis, North Dakota State University, 2020. https://hdl.handle.net/10365/31788.
Pełny tekst źródłaFonseca, Marina de Magalhães da. "Biologia reprodutiva de Butia odorata (Barb. Rodr.) Noblick". Universidade Federal de Pelotas, 2014. http://repositorio.ufpel.edu.br:8080/handle/prefix/3076.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES
Os estudos de biologia reprodutiva são fundamentais para a conservação e manejo das espécies de plantas, uma vez que o período reprodutivo é uma fase de grande importância para a dinâmica das populações e sobrevivência das espécies . Esta dissertação teve como objetivo contribuir para o conhecimento da morfologia floral, biologia floral e reprodutiva de Butia odorata (Barb. Rodr.) Noblick, além de identificar os agentes polinizadores e suas relações com as flores. O trabalho foi realizado em dois países, no Uruguai (em La Paloma, Departamento de Rocha) e no Brasil (em Porto Alegre, Rio Grande do Sul). Foram identificadas as fases de floração, antese masculina e feminina. Foi estimado o número de flores masculinas e femininas por ráquila na inflorescência, e a relação existente entre flores masculinas e femininas. Foi verificada a coloração das ráquilas e das flores. As flores foram caracterizadas quanto à sua morfologia e morfometria. Foram identificadas as ordens de insetos que visitaram as inflorescências, a relação dos insetos com as flores, os recursos florais coleta dos e o período de visitação durante as fases de floração. As flores de Butia odorata são unissexuais, hipóginas, actinomorfas, diclamídeas e sésseis. As flores masculinas e femininas ocorrem na mesma inflorescência e possuem formatos distintos, sendo as primeiras muito mais numerosas do que as segundas. As flores masculinas estão dispostas por toda a ráquila, com maior concentração do meio para o ápice, as flores femininas são encontradas do meio para a base da ráquila, formando tríades com duas masculinas. Existe variabilidade genética para cor e tamanho de ráquilas e para cor das flores em inflorescências de B. odorata. A espécie apresenta mecanismos de protandria. Uma grande diversidade de espécies de insetos das ordens Hymenoptera, Coleoptera e Diptera visitam as inflorescências. Durante a antese masculina, as ordens Hymenoptera e Coleoptera são mais frequentes, enquanto que durante a antese feminina a ordem Hymenoptera se destaca. Os insetos são atraídos pelos recursos como pólen e néctar disponibilizados pelas flores. A compreensão sobre a biologia reprodutiva, apresentado nos dois capítulos da dissertação, serve de alicerce para a preservação do butiá, pois este conhecimento é de grande importância para traçar estratégias de conservação e uso de recursos genéticos e programas de melhoramento.
Studies of reproductive biology are essential for the conservation and management of plant species, once the reproductive period is a time of great importance for the population dynamics and species survival. This dissertation had as objective to contribute to uderstanding floral morphology, floral and reproductive biology of Butia odorata (Barb. Rodr.) Noblick. Also, to identify the pollinators and their relationship with the flowers. The study was conducted in two Countries, Uruguay (La Paloma, Rocha Department) and Brazil (Porto Alegre, Rio Grande do Sul State). Stages of flowering, and male and female anthesis were identified. The number of male and female flowers per rachille in the inflorescence, and the ratio between male and female flowers were estimated. The coloring of rachilles and flowers was verified. The morphology and morphometry of flowers were characterized. Orders of insects that visited the inflorescences, the relationship of insects with flowers, the collected floral resources and the period of visitation during the stages of flowering were identified. Flowers of Butia odorata are unisexual, hypogynous, actinomorphic, dichlamydeous and sessile. The male and female flowers occur on the same inflorescence and have different formats, being the male more numerous than the female. The male flowers are arranged throughout the rachille, with higher concentration from the middle to the apex. The female flowers are found from the middle to the base of rachille, forming triads with two male flowers. There is genetic variability for color and size of rachilles and for color of flowers on inflorescences of B. odorata. The species has mechanisms of protandry. A great diversity of insects' species, belonging to the Hymenoptera, Coleoptera and Diptera orders visit the inflorescences. During male anthesis, the Hymenoptera and Coleoptera orders are more frequent, whereas during female anthesis the Hymenoptera order stands. The insects are attracted by the resources such as pollen and nectar provided by the flowers. The understanding of the reproductive biology, presented in two chapters of this dissertation, serves as the foundation for the preservation of butiá, because this knowledge is of great importance to devise strategies for the conservation and use of genetic resources and breeding programs.
Felipe, Neto Carlos Antonio Lira. "Influência da estrutura da paisagem sobre a produção e qualidade de mel da abelha jandaíra (Melipona subnitida, Apidae: Meliponini) na Caatinga". Universidade Federal Rural do Semi-Árido, 2015. http://bdtd.ufersa.edu.br:80/tede/handle/tede/394.
Pełny tekst źródłaCoordenação de Aperfeiçoamento de Pessoal de Nível Superior
Although the provision of many ecosystem services has proven affected by changes in land cover and land use, the relationship between landscape structure and the production and quality of stingless bee honey has not been studied yet. This work aimed to analyze the influence of landscape structure on the production and quality of honey from the bee Jandaira (Melipona subnitida) in Rio Grande do Norte. To do so, 15 meliponaries were selected in several areas this state, in urban and rural areas and represented by different landscape structures. Land cover was mapped in scales of 300, 1000, 2000 and 3000 meters around each meliponary. Land use was classified based on 6 classes: primary forest, secondary forest, tree crop, diverse land use, water body and urbanized area. Different landscape metrics were then calculated based on these maps, using the programs ArcGIS 10.3 and Fragstats. In each meliponary were randomly selected three colonies of M. subnitida from which a sample of honey was collected. The honey collected was sent to the laboratory for physico-chemical diagnosis (humidity, pH, water activity, reducing sugars, apparent sucrose and acidity) and assessing the sensory properties (color). The condition of the colonies was assessed by measuring the relative volume of brood cells, and honey-pots. Interviews were also performed to the beekeepers to estimate the production of honey and the number of colonies. Honey production and quality and colony condition were then related to the different landscape metrics, using a model selection approach. The results show that the proximity and amount of areas of primary forest have a positive effect on honey quality. Secondary forests had a positive effect on the pH and color of honey and a negative influence over the unused space of the boxes used to rear M. subnitida. The amount of urbanized area around the meliponaries was related negatively with honey humidity and positively with the unused space of the boxes. Hence, our work shows that protect areas of preserved Caatinga and secondary forests are important to build a refuge for pollinators and ensure the current and future provision of ecosystem services
Embora a provisão de diversos serviços ecossistêmicos tenha-se mostrado afetada por mudanças no uso e cobertura da terra, a relação entre a estrutura da paisagem e a produção e qualidade de mel de abelhas sem ferrão ainda não foi estudada. Neste trabalho analisamos a influência da estrutura da paisagem sobre a produção e a qualidade de mel da abelha jandaíra (Melipona subnitida) na Caatinga do Rio Grande do Norte. Para isso, 15 meliponários foram selecionados em diversas áreas do Estado, situados em zonas urbanas e rurais e representados por diferentes estruturas da paisagem. Fizemos mapeamentos do uso e cobertura do solo em escalas de 300, 1000, 2000 e 3000 metros ao redor de cada meliponário. As paisagens foram classificadas com base em 6 variáveis: mata primária, mata secundária, cultura arbórea, uso diverso do solo, corpo d água e área urbanizada. De acordo com esses mapeamentos, calculamos diferentes métricas da paisagem, utilizando os programas ArcGIS 10.3 e Fragstats. Em cada meliponário foram escolhidas aleatoriamente três colônias de M. subnitida. De cada colônia foi retirada uma amostra de mel. O mel coletado foi encaminhado ao laboratório da UFERSA para diagnóstico físico-químico (umidade, pH, atividade de água, açúcares redutores, sacarose aparente e acidez) e sensorial (cor). Das colônias selecionadas também foram realizadas medições (comprimento, altura e largura) dos favos de cria, dos potes de mel e da caixa racional para avaliação da condição da colônia. Fizemos também entrevistas aos meliponicultores sobre a produção de mel e quantidade de colônias no meliponário. Os dados de produção e qualidade de mel, bem como de condição das colônias, foram então relacionados com as diferentes métricas da paisagem, utilizando um procedimento de seleção de modelos. Os resultados mostraram que a proximidade e quantidade de áreas de mata primária tiveram um efeito nos parâmetros de qualidade do mel. A classe da paisagem mata secundária teve efeito positivo no pH e na coloração do mel e negativo no espaço não utilizado das caixas racionais de criação de M. subnitida. Já a quantidade de área urbanizada ao redor dos meliponários relacionou-se de maneira negativa com a umidade do mel e positiva com o espaço não utilizado das caixas racionais. Portanto, proteger as áreas de caatinga preservada e as matas secundárias é a base para alicerçamos o refúgio para os polinizadores e garantir os seus serviços ecossistêmicos para o presente e futuro
Lima-Verde, Luiz Wilson. "Melissofaunistic resources of the Baturità mountains, CearÃ, Brazil â diversity and husbandry potential". Universidade Federal do CearÃ, 2011. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=7391.
Pełny tekst źródłaChambó, Emerson Dechechi. "Polinização em genótipos de girassol (Helianthus annuus L.)". Universidade Estadual do Oeste do Paraná, 2010. http://tede.unioeste.br:8080/tede/handle/tede/1610.
Pełny tekst źródłaThe Research consisted of three experiments in Marechal Cândido Rondon city - PR, Brazil. In the first experiment the objective was to verify the influence of Apis Mellifera L. pollination on productive and physiological traits in sunflower achenes. The treatments were constituted by the combination of eight sunflower genotypes (Multissol, M734, Catissol 01, Charrua, MG2, Aguará, Helio 360 and Embrapa 122) and two tests of pollination, i) the flowers were free to insect visitation and ii) pollinators were restricted to visiting only inflorescences protected with gauze. The parameters analyzed were total productivity of seeds (PS), number of achenes per inflorescence (NA), mass of achenes per inflorescence (MA), mass of chapters (MC), chapter diameter (CD), ether extract in the achenes (EE), germination (GE), and mass of 1000 achenes (M1000). It was verified that the sunflower plants of the hybrid M734, exposed to insect pollination, showed PS and NA equal to 91,07% and 42,03%, respectively higher (p<0,05) than the plants of this hybrid with inflorescences protected with gauze. The chapters of the Catissol 01 cultivar exposed to insect pollination showed MA, MC and CD respectively, 150,52%, 130,28% e 35,06%, higher than the chapters of this cultivar protected with gauze. Inflorescences of the Embrapa 122 cultivar, free to insect visitation, presented EE and GE respectively, 52,63% e 134,29%, higher (p<0,05), than the inflorescences of this cultivar protected with gauze. Sunflower plants pollinated by Apis Mellifera presented average percentage of M1000 of 22,32% higher (p<0,05) than the plants protected with gauze, regardless of which genotype was being studied. In general, the pollination by insects enhances the productive traits and the quality of the seeds of sunflower genotypes. The second experiment was carried out with the objective of observing the type of food that africanized honey bees collect (pollen or nectar) at different times of day during the flowering period of five sunflower genotypes. The experimental design was arranged in randomized blocks split-plots scheme, with 100 treatments, four replications and two plants per experimental unit. The treatments were constituted by the combination of five genotypes of sunflower and (Helio 360, Helio 251, Charrua, Aguará e Multissol) allocated to plots and five days of observation and four time slots arranged in subplots. It could be seen that on the second and third days of sunflowers flowering there was a higher number of visits of Apis mellifera collecting nectar. It was observed that the honey bees collect pollen and nectar all they long, with peaks of collections from 7 to 8:30AM. The average density of honey bees throughout the day was 2.27 to 2.94 bees per inflorescence, and the honey bees collecting nectar were more frequent (2.28 bees / inflorescence) than honey bees collecting pollen (0.40 bees/inflorescence) on flowering days 2,94 and 2,96, respectively, and during the most visited time in the culture (7: 00 to 8:30 AM). On the third day of flowering, the hybrid Helio 360 and Aguará showed no differences amongst each other, and also showed higher (p <0.05) number of visitations of honey bees per inflorescence as compared to the other genotypes analyzed in the present study. It can be concluded that the africanized honey bees prefer to do their work of collecting food between the second and third day of flowering, between 7:00 to 8:30AM. Moreover, the hybrids Helio 360 and Aguará are more attractive to honeybees and should be recommended for maintenance and increase of number of pollinators in cultivated areas and to expand programs of honeybees pasture in the western of Paraná state, Brazil. The third experiment was carried out to evaluate the effect of the use of insecticide imidacloprid + beta-cyfluthrin on the number of visits by Apis mellifera bees to four sunflowers during the flowering season. Five plants were marked before the period of flowering of hybrids M734, Charrua, Helio 250 e Aguará, with four repetitions. Two observers remained two minutes on each plant, counting the number of honeybees in two intervals of time (from 8:30 AM to 10:00 AM and from 3:30 PM to 5:00 PM). The counting took place before the application of insecticide and twelve hours after the use of the product. It was verified that there was a significant negative effect of insecticide on the bees visitation considering the data of all hybrids, the hybrid of the M734 and Aguará. There was no effect of insecticide on the visit considering the data of the hybrid Charrua and Helio 250. It was also verified that the insecticide imidacloprid + beta-cyfluthrin causes repellence of Apis mellifera in sunflower crop. Moreover, the insecticide imidacloprid + beta-cyfluthrin was harmless to adults of Apis mellifera during blooming period for sunflowers, when applied to the lower middle third of the plants and the period in which these honeybees were not foraging. It would be necessary to assess their possible effects on young stages for further use in programs of integrated pest management in sunflower crop
A pesquisa constou de três experimentos, no município de Marechal Cândido Rondon, Paraná. No experimento I, objetivou-se verificar a influência da polinização realizada por Apis mellifera L. sobre características produtivas e fisiológicas em aquênios de girassol. Os tratamentos foram constituídos pela combinação de oito genótipos de girassol (Multissol, M734, Catissol 01, Charrua, MG2, Aguará, Helio 360 e Embrapa 122), casualizados nas parcelas, e dois testes de polinização, um livre a ação de insetos e o outro restringindo os polinizadores com sacos de filó, que foram alocados nas subparcelas. Os parâmetros analisados foram produtividade total de grãos (PT), número de aquênios por inflorescência (NA), massa de aquênios por inflorescência (MA), massa de capítulo (MC), diâmetro de capítulo (DC), teor de extrato etéreo em aquênios (EE), germinação (GE) e massa de 1000 aquênios (M1000). Verificou-se que as plantas de girassol do híbrido M734 expostas à polinização entomófila apresentaram PT e NA de 91,07% e 42,03%, respectivamente maiores (p<0,05) do que as plantas desse híbrido com inflorescências protegidas com filó. Os capítulos de girassol da variedade Catissol 01 expostos à polinização entomófila apresentaram MA, MC e DC de 150,52%, 130,28% e 35,06%, respectivamente maiores (p<0,05) do que os capítulos dessa variedade protegidos com filó. Inflorescências de girassol da variedade Embrapa 122 que ficaram livres a ação de insetos apresentaram EE e GE de 52,63% e 134,29%, respectivamente maiores (p<0,05) do que as inflorescências dessa variedade protegidas com filó. Plantas de girassol polinizadas por insetos apresentaram porcentagem média de M1000 de 22,32% maior (p<0,05) do que as plantas restringidas aos polinizadores por filó, independentemente do híbrido estudado. De maneira geral, a polinização entomófila aumenta as características produtivas e qualidade fisiológica em aquênios de girassol. O ensaio II foi conduzido com o objetivo de observar o comportamento de coleta de alimentos (néctar e pólen) de A. mellifera em cinco genótipos de girassol, em diferentes horários do dia, durante o período de florescimento da cultura. O delineamento experimental empregado foi o de blocos casualizados completos em esquema de parcelas subdivididas no tempo, com 100 tratamentos, quatro repetições e duas plantas por unidade experimental. Os tratamentos foram constituídos pela combinação de cinco genótipos de girassol (Helio 360, Helio 251, Charrua, Aguará e Multissol), alocados nas parcelas e cinco dias de observação e quatro intervalos de tempo arranjados nas subparcelas. Verificou-se pico de visitas de A. mellifera para coleta de néctar entre o segundo e terceiro dia de florescimento na cultura do girassol. Observou-se que as abelhas realizam coletas de pólen e néctar ao longo de todo o dia, com pico de coleta no período das 7 às 8h30min. A densidade média de A. mellifera ao longo do dia foi de 2,27 a 2,94 abelhas por inflorescência, sendo as abelhas coletoras de néctar mais frequentes (2,28 abelhas/inflorescência) do que as coletoras de pólen (0,40 abelhas/inflorescência) no dia de florescimento 2,94 e 2,96, respectivamente e no horário de maior visitação na cultura (7h às 08h30min). No terceiro dia do florescimento, os híbridos Helio 360 e Aguará não diferiram entre si e apresentaram maiores (p<0,05) números de visitas de abelhas por inflorescência em relação aos demais genótipos estudados. As abelhas africanizadas preferem realizar suas coletas de néctar e pólen entre o segundo e terceiro dia do florescimento do girassol, no horário das 7 às 8h30min. Os híbridos de girassol Helio 360 e Aguará são mais atrativos à A.mellifera e devem ser recomendados para manutenção e aumento de polinizadores em áreas cultivadas, bem como para pasto apícola na região Oeste do Paraná. No terceiro experimento objetivou-se verificar o efeito da aplicação do inseticida imidacloprido + beta-ciflutrina sobre a visitação de abelhas às inflorescências de quatro híbridos de girassol, durante o florescimento da cultura. Foram marcadas cinco plantas antes do período de florescimento dos híbridos M734, Charrua, Aguará e Helio 250, com quatro repetições. Dois observadores permaneceram dois minutos em cada inflorescência, contando o número de abelhas visitantes em dois intervalos de tempo (8h30min às 10h e 15h30min ás 17h). A contagem ocorreu antes da aplicação do inseticida e 12 horas após a utilização do produto na plantação. Houve efeito significativo de inseticida sobre a visitação de abelhas considerando os dados de todos os híbridos, do híbrido M734 e Aguará, sendo menor o número de visitas de abelhas africanizadas às inflorescências após a aplicação do produto. Não houve efeito de inseticida sobre a visitação nos híbridos Charrua e Helio 250. Constatou-se que o inseticida imidacloprido + beta-ciflutrina causa repelência a A. mellifera na cultura do girassol. Além disso, o inseticida imidacloprido + beta-ciflutrina foi inofensivo aos adultos de A. mellifera, durante o florescimento do girassol, quando aplicado no terço médio inferior das plantas e no período em que essas abelhas não estavam forrageando, sendo necessária a avaliação de seus possíveis efeitos em fases jovens para posterior utilização em programas de manejo integrado de pragas na cultura do girassol
Książki na temat "Floral resources"
Sano, Sueli Matiko, Semíramis Pedrosa de Almeida i José Felipe Ribeiro. Cerrado: Ecologia e flora. Redaktor Embrapa Cerrados. Brasília, DF: Embrapa Informação Tecnológica, 2008.
Znajdź pełny tekst źródłaJuan L. R. Ricart Pujols. Sinópsis anotada y comentada de la flora del bosque estatal de Maricao. United States: Forest Service, U.S. Department of Agriculture, 2010.
Znajdź pełny tekst źródłaSpain. Espacios naturales protegidos, flora y fauna: Legislación básica comentada. Madrid: Exlibris Ediciones, 1996.
Znajdź pełny tekst źródłaMejía, Cristina Matiz. Flora medicinal y sus conocimientos asociados: Lineamientos para una regulación. Bogotá D.C: Universidad del Rosario, Facultad de Jurisprudencia, Facultad de Medicina, 2007.
Znajdź pełny tekst źródłaMejía, Cristina Matiz. Flora medicinal y sus conocimientos asociados: Lineamientos para una regulación. Bogotá D.C: Universidad del Rosario, Facultad de Jurisprudencia, Facultad de Medicina, 2007.
Znajdź pełny tekst źródłaParker, James N., i Philip M. Parker. Flomax: A medical dictionary, bibliography and annotated research guide to Internet references. San Diego, CA: ICON Health Publications, 2003.
Znajdź pełny tekst źródłaPrescott-Allen, Robert. Cuánto vale la vida silvestre?: Las contribuciones económicas que la flora y fauna silvestres aportan a los países en vías de desarrollo. Cusco, Peru: Centro de Estudios Rurales Andinos "Bartolomé de Las Casas", 1987.
Znajdź pełny tekst źródłaUnited States. Congress. House. Committee on Resources. Subcommittee on Fisheries Conservation, Wildlife, and Oceans. Twelfth regular meeting of COP12 of CITES: Oversight hearing before the Subcommittee on Fisheries Conservation, Wildlife, and Oceans of the Committee on Resources, U.S. House of Representatives, One Hundred Eighth Congress, first session, February 25, 2003. Washington: U.S. G.P.O., 2003.
Znajdź pełny tekst źródłaHebei shan di gao deng zhi wu qu xi yu zhen xi bin wei zhi wu zi yuan: Higher plant flora and rare and endangered plant resources in Hebei mountains region. Beijing: Ke xue chu ban she, 2010.
Znajdź pełny tekst źródłaMilans, Flora H. The Nuclear Regulatory Commission's proposed withdrawal from participation in the Small Business Innovation Research Program: Statement of Flora H. Milans, Associate Director, Resources, Community, and Economic Development Division, before the House Committee on Small Business. [Washington, D.C.?]: U.S. General Accounting Office, 1988.
Znajdź pełny tekst źródłaCzęści książek na temat "Floral resources"
Abrol, Dharam P. "Floral Resources". W Asiatic Honeybee Apis cerana, 431–508. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6928-1_12.
Pełny tekst źródłaChauhan, Avinash, i H. K. Singh. "Distribution, Nesting Biology and Floral Resources of Red Dwarf Honeybee (Apis florea Fabricius) in Nagaland, India". W The Future Role of Dwarf Honeybees in Natural and Agricultural Systems, 295–300. First edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9781003033936-22.
Pełny tekst źródłaPérez, V. "Seasonal Dynamic of the Vegetation at “Los Carneros” Lagoon: Handled Floral Reserve Sabanalamar-San Ubaldo, Pinar del Río, Cuba". W Management of Water Resources in Protected Areas, 309–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-16330-2_36.
Pełny tekst źródłaRaju, A. J. Solomon. "Morphometric Variation and Floral Resources of the Dwarf Honeybee, Apis florea F. in Andhra Pradesh and Telangana, India". W The Future Role of Dwarf Honeybees in Natural and Agricultural Systems, 169–84. First edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9781003033936-13.
Pełny tekst źródłaLayek, Ujjwal, i Prakash Karmakar. "Distribution, Nesting Biology and Floral Resources of Red Dwarf Honey Bee (Apis florea Fabricius) in West Bengal, India". W The Future Role of Dwarf Honeybees in Natural and Agricultural Systems, 301–9. First edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9781003033936-23.
Pełny tekst źródłaAshman, Tia-Lynn, i Daniel J. Schoen. "Floral Longevity: Fitness Consequences and Resource Costs". W Floral Biology, 112–39. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1165-2_5.
Pełny tekst źródłaBenfield, Richard W. "Future directions." W New directions in garden tourism, 156–68. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789241761.0156.
Pełny tekst źródłaBenfield, Richard W. "Future directions." W New directions in garden tourism, 156–68. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789241761.0011.
Pełny tekst źródłavan der Kloet, P., i H. de Niet. "The Reduction of the Effects on Flora Caused by Drainage Water Quality by a Proposed Reservoir as an Element of a Feedbacksystem". W Hydraulic Design in Water Resources Engineering: Land Drainage, 465–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-22014-6_44.
Pełny tekst źródłaNazir, Muslima, Roohi Mushtaq, Showkat Ahmad Zargar, Aijaz Ahmad Wani i Sajad Majeed Zargar. "Therapeutic Potential of Plant Genetic Resources and Traditional Knowledge: A Panoramic View of the Flora Indigenous to North West Himalayas". W Plant Genetic Resources and Traditional Knowledge for Food Security, 255–66. Singapore: Springer Singapore, 2015. http://dx.doi.org/10.1007/978-981-10-0060-7_15.
Pełny tekst źródłaStreszczenia konferencji na temat "Floral resources"
Lowe, Abigail, Laura Jones, Col Ford, Matthew Hegarty, Simon Creer i Natasha de Vere. "Investigating the value of gardens for providing floral resources to pollinating insects". W 5th European Congress of Conservation Biology. Jyväskylä: Jyvaskyla University Open Science Centre, 2018. http://dx.doi.org/10.17011/conference/eccb2018/107582.
Pełny tekst źródłaSimao, Maria-Carolina M. "How many flowers are enough? Increasing floral resources to maintain pollinator diversity (syrphid flies and halictid bees) in an urban landscape". W 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.112936.
Pełny tekst źródłaKuder, Lisa J. "Pollinator habitat along highway rights-of-way: Preliminary results of a comparison of pollinator communities under different meadow management regimes and quantification of common roadside pollutants in floral resources of adjacent wildflowers". W 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.110562.
Pełny tekst źródłaBotev, Jean, i Steffen Rothkugel. "FloRA - Flock-Based Resource Allocation for Decentralized Distributed Virtual Environments". W 4th International ICST Conference on Simulation Tools and Techniques. ACM, 2011. http://dx.doi.org/10.4108/icst.simutools.2011.245544.
Pełny tekst źródłaDamci, Atilla, Gul Polat, Firat Dogu Akin i Harun Turkoglu. "Resource Levelling with Float Consumption Rate". W Creative Construction Conference 2019. Budapest University of Technology and Economics, 2019. http://dx.doi.org/10.3311/ccc2019-082.
Pełny tekst źródłaShala, Albona. "THE IMPACT OF POLLUTED RIVER SITNICA IN FLORA AND VEGETATION AROUND THE RIVER". W 14th SGEM GeoConference on WATER RESOURCES. FOREST, MARINE AND OCEAN ECOSYSTEMS. Stef92 Technology, 2014. http://dx.doi.org/10.5593/sgem2014/b32/s14.063.
Pełny tekst źródłaBatoro, Jati. "Flora krandan (Canavalia maritima (Aubl.) Urb. in South Coastal Java, Indonesia". W THE 9TH INTERNATIONAL CONFERENCE ON GLOBAL RESOURCE CONSERVATION (ICGRC) AND AJI FROM RITSUMEIKAN UNIVERSITY. Author(s), 2018. http://dx.doi.org/10.1063/1.5061842.
Pełny tekst źródłaSánchez, Aramis A., Marena M. Herrera, Javier F. Carrión i Mercedes A. Villa. "Detection of heavy metals in hydric resources through the optical analysis of exposed flora". W Light in Nature VII, redaktorzy Joseph A. Shaw, Katherine Creath i Vasudevan Lakshminarayanan. SPIE, 2019. http://dx.doi.org/10.1117/12.2529857.
Pełny tekst źródłaGuo, Haibin. "Analysis of Multi-Resources Leveling Problem with Risk Float Time". W 2011 International Conference on Intelligent Computation Technology and Automation (ICICTA). IEEE, 2011. http://dx.doi.org/10.1109/icicta.2011.198.
Pełny tekst źródłaGuerrero, Melissa Yvette. "Floral resource used by colonies ofBombus atratus (Hymenoptera: Apidae) on the campus Nueva Granada Military University, Cajicá, Colombia". W 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.109821.
Pełny tekst źródłaRaporty organizacyjne na temat "Floral resources"
Wallace, Hailey. Are We Providing Preferred Floral Resources for Bees in Our Neighborhoods?: Assessing the Relationship Between Small Scale Vegetation Metrics and Bee Presence in SE Portland. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.7005.
Pełny tekst źródłaHenderson, Tim, Mincent Santucci, Tim Connors i Justin Tweet. National Park Service geologic type section inventory: Chihuahuan Desert Inventory & Monitoring Network. National Park Service, kwiecień 2021. http://dx.doi.org/10.36967/nrr-2285306.
Pełny tekst źródłaHenderson, Tim, Vincent Santucci, Tim Connors i Justin Tweet. National Park Service geologic type section inventory: Northern Colorado Plateau Inventory & Monitoring Network. National Park Service, kwiecień 2021. http://dx.doi.org/10.36967/nrr-2285337.
Pełny tekst źródłaHenderson, Tim, Vincent Santucci, Tim Connors i Justin Tweet. National Park Service geologic type section inventory: Klamath Inventory & Monitoring Network. National Park Service, lipiec 2021. http://dx.doi.org/10.36967/nrr-2286915.
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