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1.
Nat Commun ; 15(1): 4834, 2024 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-38844446

RESUMO

Oceanic eddies are recognized as pivotal components in marine ecosystems, believed to concentrate a wide range of marine life spanning from phytoplankton to top predators. Previous studies have posited that marine predators are drawn to these eddies due to an aggregation of their forage fauna. In this study, we examine the response of forage fauna, detected by shipboard acoustics, across a broad sample of a thousand eddies across the world's oceans. While our findings show an impact of eddies on surface temperatures and phytoplankton in most cases, they reveal that only a minority (13%) exhibit significant effects on forage fauna, with only 6% demonstrating an oasis effect. We also show that an oasis effect can occur both in anticyclonic and cyclonic eddies, and that the few high-impact eddies are marked by high eddy amplitude and strong water-mass-trapping. Our study underscores the nuanced and complex nature of the aggregating role of oceanic eddies, highlighting the need for further research to elucidate how these structures attract marine predators.


Assuntos
Ecossistema , Oceanos e Mares , Fitoplâncton , Animais , Fitoplâncton/fisiologia , Temperatura , Organismos Aquáticos/fisiologia , Comportamento Predatório/fisiologia , Acústica
2.
PLoS One ; 18(8): e0284953, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37540685

RESUMO

Ocean dynamics initiate the structure of nutrient income driving primary producers, and these, in turn, shape the distribution of subsequent trophic levels until the whole pelagic community reflects the physicochemical structure of the ocean. Despite the importance of bottom-up structuring in pelagic ecosystems, fine-scale studies of biophysical interactions along depth are scarce and challenging. To improve our understanding of such relationships, we analyzed the vertical structure of key oceanographic variables along with the distribution of acoustic biomass from multi-frequency acoustic data (38, 70, and 120 kHz) as a reference for pelagic fauna. In addition, we took advantage of species distribution databases collected at the same time to provide further interpretation. The study was performed in the Southwestern Tropical Atlantic of northeast Brazil in spring 2015 and autumn 2017, periods representative of canonical spring and autumn conditions in terms of thermohaline structure and current dynamics. We show that chlorophyll-a, oxygen, current, and stratification are important drivers for the distribution of sound scattering biota but that their relative importance depends on the area, the depth range, and the diel cycle. Prominent sound scattering layers (SSLs) in the epipelagic layer were associated with strong stratification and subsurface chlorophyll-a maximum. In areas where chlorophyll-a maxima were deeper than the peak of stratifications, SSLs were more correlated with stratification than subsurface chlorophyll maxima. Dissolved oxygen seems to be a driver in locations where lower oxygen concentration occurs in the subsurface. Finally, our results suggest that organisms seem to avoid strong currents core. However, future works are needed to better understand the role of currents on the vertical distribution of organisms.


Assuntos
Clorofila , Ecossistema , Clorofila A , Biomassa , Brasil , Oceano Atlântico
3.
Rev. cuba. hematol. inmunol. hemoter ; 30(3): 249-256, jul.-set. 2014.
Artigo em Espanhol | LILACS | ID: lil-723762

RESUMO

Introducción: la obtención de anticuerpos monoclonales en líquido ascítico ha ido decayendo paulatinamente por la aparición de alternativas de producción in Vitro, que permiten alcanzar mayores volúmenes y un control más riguroso del proceso productivo, lo que incrementa la reproducibilidad de procesos y la calidad de los productos. Objetivo: evaluar dos métodos de producción de sobrenadante de cultivo rico en una inmunoglobulina de ratón del tipo IgG2b, aglutinadora de hematíes humanos portadores del antígeno del grupo sanguíneo B, según el sistema ABO; la cual es secretada por el hibridoma C6G4. Métodos: se evaluaron dos métodos de producción del anticuerpo con el empleo de un biorreactor CELLine, útil como modelo para la obtención de anticuerpos monoclonales en cultivos de alta densidad celular. Los métodos se diferenciaron esencialmente en la densidad celular de siembra en el biorreactor y en la duración del periodo de fermentación entre la siembra y la cosecha del caldo de cultivo rico en anticuerpos. Para cada método se determinó la concentración específica de anticuerpos y la potencia de aglutinación del sobrenadante, así como la densidad y la viabilidad celular del cultivo alcanzadas en el momento de la cosecha. Resultados: se observó que ambos métodos generaron sobrenadantes de cultivo con una potencia de aglutinación similar, a pesar de que se encontraron diferencias en el resto de las variables medidas. Si bien uno de los métodos produjo una mayor concentración de anticuerpos en el sobrenadante, no se observaron diferencias en la potencia de aglutinación de los sobrenadantes obtenidos por ambas alternativas. Conclusiones: los dos métodos estudiados permitieron obtener volúmenes semejantes de sobrenadante anti-B con diferentes concentraciones de anticuerpos, pero con una potencia de aglutinación similar. La principal diferencia residió en que uno de los métodos permitió obtener el mismo volumen del producto en un tiempo sensiblemente menor...


Introduction : the obtention of monoclonal antibodies in ascite fluid has been declining gradually due to the appearance of alternative in vitro production that achieve higher volumes and a more precise monitoring of the production process, which increases the reproducibility of processes and the quality of products. Objective : to evaluate two methods to make cell culture supernatant rich in murine monoclonal IgG2b type, with agglutinating activity against human red cell of blood group antigen B (ABO system), which is secreted by murine hybridoma C6G4. Methods : two methods were evaluated for antibody production in cell culture supernatant using as model a CELLine bioreactor for the production of monoclonal antibodies in high cell density culture. Both methods essentially differed in the seeding cell density in the bioreactor and the fermentation period between seeding and harvesting of the culture broth rich in antibodies. The specific antibody concentration and potency of agglutination was determined in the obtained supernatant and also the cell density and cell viability of the culture reached at the time of harvest. Results : both methods generated culture supernatants with similar agglutination strength despite differences found in the rest of the variables measured. Even when one of the methods produced a higher antibody concentration in the supernatants, no differences in potency of the supernatants agglutination obtained by both alternatives were observed. Conclusions : both methods generated supernatant anti-B with different concentrations of antibodies but similar potency of agglutination. The main difference was that with one of the methods the same volume of the product was obtained in a considerably minor time...


Assuntos
Humanos , Antígenos de Grupos Sanguíneos , Formação de Anticorpos/fisiologia , Imunoglobulina G/uso terapêutico , Testes de Aglutinação/métodos , Reatores Biológicos/microbiologia , Sistema ABO de Grupos Sanguíneos
4.
PLoS One ; 9(7): e102354, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25047077

RESUMO

The submarine volcano eruption off El Hierro Island (Canary Islands) on 10 October 2011 promoted dramatic perturbation of the water column leading to changes in the distribution of pelagic fauna. To study the response of the scattering biota, we combined acoustic data with hydrographic profiles and concurrent sea surface turbidity indexes from satellite imagery. We also monitored changes in the plankton and nekton communities through the eruptive and post-eruptive phases. Decrease of oxygen, acidification, rising temperature and deposition of chemicals in shallow waters resulted in a reduction of epipelagic stocks and a disruption of diel vertical migration (nocturnal ascent) of mesopelagic organisms. Furthermore, decreased light levels at depth caused by extinction in the volcanic plume resulted in a significant shallowing of the deep acoustic scattering layer. Once the eruption ceased, the distribution and abundances of the pelagic biota returned to baseline levels. There was no evidence of a volcano-induced bloom in the plankton community.


Assuntos
Biota , Erupções Vulcânicas/análise , Acústica , Migração Animal , Animais , Evolução Biológica , Desastres , Ecossistema , Luz , Plâncton/fisiologia , Células Procarióticas , Água do Mar/análise , Espanha
5.
Biotechnol Appl Biochem ; 48(Pt 3): 159-65, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17523917

RESUMO

Human proteins are not routinely expressed at high levels in Escherichia coli for, among other reasons, different codon usage. Several purification procedures have been applied to recover recombinant proteins for further biological characterization. However, the vast majority involve costly chromatography procedures. In the present study, both (Hu)IFN(alpha 2b) (human interferon alpha 2b) and (Hu)IFN(alpha 8) were expressed efficiently in E. coli BL21-codonplus-RIL. Subsequently, both recombinant proteins were purified to homogeneity by passive elution from reverse-stained SDS/PAGE gels, a cost-effective purification procedure. After purification, both recovered proteins were biologically active. The (Hu)IFN(alpha 8) subtype induced 1.46-fold more antiviral activity than (Hu)IFN(alpha 2b) using Hep-2 human laryngeal carcinoma cell challenged with Mengo virus.


Assuntos
Antivirais/farmacologia , Interferon-alfa/farmacologia , Interferons/fisiologia , Mengovirus/efeitos dos fármacos , Mengovirus/imunologia , Sequência de Aminoácidos , Sequência de Bases , Linhagem Celular Tumoral , Escherichia coli , Humanos , Interferon alfa-2 , Interferon-alfa/biossíntese , Interferon-alfa/genética , Interferons/biossíntese , Interferons/genética , Dados de Sequência Molecular , Proteínas Recombinantes
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