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1.
Nature ; 608(7923): 558-562, 2022 08.
Artículo en Inglés | MEDLINE | ID: mdl-35948632

RESUMEN

The productivity of rainforests growing on highly weathered tropical soils is expected to be limited by phosphorus availability1. Yet, controlled fertilization experiments have been unable to demonstrate a dominant role for phosphorus in controlling tropical forest net primary productivity. Recent syntheses have demonstrated that responses to nitrogen addition are as large as to phosphorus2, and adaptations to low phosphorus availability appear to enable net primary productivity to be maintained across major soil phosphorus gradients3. Thus, the extent to which phosphorus availability limits tropical forest productivity is highly uncertain. The majority of the Amazonia, however, is characterized by soils that are more depleted in phosphorus than those in which most tropical fertilization experiments have taken place2. Thus, we established a phosphorus, nitrogen and base cation addition experiment in an old growth Amazon rainforest, with a low soil phosphorus content that is representative of approximately 60% of the Amazon basin. Here we show that net primary productivity increased exclusively with phosphorus addition. After 2 years, strong responses were observed in fine root (+29%) and canopy productivity (+19%), but not stem growth. The direct evidence of phosphorus limitation of net primary productivity suggests that phosphorus availability may restrict Amazon forest responses to CO2 fertilization4, with major implications for future carbon sequestration and forest resilience to climate change.


Asunto(s)
Cambio Climático , Fósforo , Bosque Lluvioso , Suelo , Árboles , Clima Tropical , Aclimatación , Dióxido de Carbono/metabolismo , Dióxido de Carbono/farmacología , Secuestro de Carbono , Cationes/metabolismo , Cationes/farmacología , Cambio Climático/estadística & datos numéricos , Modelos Biológicos , Nitrógeno/metabolismo , Nitrógeno/farmacología , Fósforo/metabolismo , Fósforo/farmacología , Suelo/química , Árboles/efectos de los fármacos , Árboles/metabolismo , Incertidumbre
2.
New Phytol ; 230(1): 116-128, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33341935

RESUMEN

Soil nutrient availability can strongly affect root traits. In tropical forests, phosphorus (P) is often considered the main limiting nutrient for plants. However, support for the P paradigm is limited, and N and cations might also control tropical forests functioning. We used a large-scale experiment to determine how the factorial addition of nitrogen (N), P and cations affected root productivity and traits related to nutrient acquisition strategies (morphological traits, phosphatase activity, arbuscular mycorrhizal colonisation and nutrient contents) in a primary rainforest growing on low-fertility soils in Central Amazonia after 1 yr of fertilisation. Multiple root traits and productivity were affected. Phosphorus additions increased annual root productivity and root diameter, but decreased root phosphatase activity. Cation additions increased root productivity at certain times of year, also increasing root diameter and mycorrhizal colonisation. P and cation additions increased their element concentrations in root tissues. No responses were detected with N addition. Here we showed that rock-derived nutrients determined root functioning in low-fertility Amazonian soils, demonstrating not only the hypothesised importance of P, but also highlighting the role of cations. The changes in fine root traits and productivity indicated that even slow-growing tropical rainforests can respond rapidly to changes in resource availability.


Asunto(s)
Fósforo , Clima Tropical , Cationes , Bosques , Nitrógeno/análisis , Raíces de Plantas/química , Suelo , Árboles
3.
BMC Res Notes ; 5: 128, 2012 Mar 06.
Artículo en Inglés | MEDLINE | ID: mdl-22395020

RESUMEN

BACKGROUND: Rhodnius prolixus is a blood-feeding insect that can transmit Trypanosoma cruzi and Trypanosoma rangeli to vertebrate hosts. Recently, genomic resources for invertebrate vectors of human pathogens have increased significantly, and R. prolixus has been one of the main species studied among the triatomines. However, the paucity of information on many of the fundamental molecular aspects of this species limits the use of the available genomic information. The present study aimed to facilitate gene expression studies by identifying the most suitable reference genes for the normalization of mRNA expression data from qPCR. RESULTS: The expression stability of five candidate reference genes (18S rRNA, GAPDH, ß-actin, α-tubulin and ribosomal protein L26) was evaluated by qPCR in two tissues (salivary gland and intestine) and under different physiological conditions: before and after blood feeding and after infection with T. cruzi or T. rangeli. The results were analyzed with three software programs: geNorm, NormFinder and BestKeeper. All of the evaluated candidate genes proved to be acceptable as reference genes, but some were found to be more appropriate depending on the experimental conditions. 18S, GAPDH and α-tubulin showed acceptable stability for studies in all of the tissues and experimental conditions evaluated. ß-actin, one of the most widely used reference genes, was confirmed to be one of the most suitable reference genes in studies with salivary glands, but it had the lowest expression stability in the intestine after insect blood feeding. L26 was identified as the poorest reference gene in the studies performed. CONCLUSIONS: The expression stability of the genes varies in different tissue samples and under different experimental conditions. The results provided by three statistical packages emphasize the suitability of all five of the tested reference genes in both the crop and the salivary glands with a few exceptions. The results emphasise the importance of validating reference genes for qRT-PCR analysis in R. prolixus studies.


Asunto(s)
Expresión Génica , Genes Esenciales , Mucosa Intestinal/metabolismo , Rhodnius/genética , Glándulas Salivales/metabolismo , Programas Informáticos , Animales , Perfilación de la Expresión Génica , Gliceraldehído-3-Fosfato Deshidrogenasa (Fosforilante)/genética , Intestinos/citología , ARN Ribosómico 18S/genética , Reacción en Cadena en Tiempo Real de la Polimerasa/normas , Estándares de Referencia , Rhodnius/parasitología , Glándulas Salivales/citología , Trypanosoma cruzi/fisiología , Trypanosoma rangeli/fisiología , Tubulina (Proteína)/genética
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