Negative effects of ant-plant interaction on pollination: costs of a mutualism

The mutualism of ants and extrafloral nectary (EFN)-bearing plants is known to reduce rates of herbivory. However, ants may have negative impacts on other mutualisms such as pollination, constituting an indirect cost of a facultative mutualism. For instance, when foraging on or close to reproductive plant parts ants might attack pollinators or inhibit their visits. We tested the hypothesis that ants on EFN-bearing plants may negatively influence pollinator behavior, ultimately reducing plant fitness (fruit set). The study was done in a reserve at Brazilian savannah using the EFN-bearing plant Banisteriopsis malifolia (Malpighiaceae). The experimental manipulation was carried out with four groups: control (free visitation of ants), without ants (ant-free branches), artificial ants (isolated branches with artificial ants on flowers) and plastic circles (isolated branches with plastic circles on flowers). We made observations on flower visitors and their interactions, and measured fruit formation as a proxy for plant fitness. Our results showed that pollinators hesitated to visit flowers with artificial ants, negatively affecting pollination, but did not hesitate to visit flowers with plastic circles, suggesting that they recognize the specific morphology of the ants. Pollinators spent more time per flower on the ant-free branches, and the fruiting rate was lower in the group with artificial ants. Our results confirm an indirect cost in this facultative mutualism, where the balance between these negative and positive effects of ants on EFN-bearing plants are not well known

Four-Loop Decoupling Relations for the Strong Coupling

We compute the matching relation for the strong coupling constant within the framework of QCD up to four-loop order. This allows a consistent five-loop running (once the $\beta$ function is available to this order) taking into account threshold effects. As a side product we obtain the effective coupling of a Higgs boson to gluons with five-loop accuracy.Comment: 11 page

Higher Order Statistics in a mmWave Propagation Environment

(c) 2019 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other users, including reprinting/ republishing this material for advertising or promotional purposes, creating new collective works for resale or redistribution to servers or lists, or reuse of any copyrighted components of this work in other works.[EN] A thorough measurement campaign in an indoor environment at the millimeter-wave band is carried out with an aim at characterizing the short-term fading channel in terms of its higher-order statistics. The measurements are conducted in a variety of scenarios, with frequencies ranging from 55 to 65 GHz, in line-of-sight and non-line-of-sight conditions, and combinations of horizontal and vertical polarizations at both the transmitter and the receiver. A number of fading models are tested, namely Rayleigh, Rice, Nakagami-m, alpha-mu, kappa-mu, eta-mu, and alpha-eta-kappa-mu. The main second-order statistics under analysis are the level crossing rate (LCR) and average fade duration (AFD) both given per distance unit. From the experimental data, the parameters of these statistics are estimated, and the corresponding curves of the theoretical models are compared with the empirical ones and the best model is selected. Additionally, the study of the very general distribution, namely alpha-eta-kappa-mu, is advanced, in which new expressions for time-/distance-domain LCR and Al-ll are derived using an envelope-based approach. Such an approach leads to integral-form formulations with much less computational complexity and computes rapidly compared with the already existing ones presented elsewhere, also given in the integral form. Furthermore, a series of expansion expression for the alpha-eta-kappa-mu time-/distance-domain LCR is then derived that improves even further the computational time.This work was supported in part by the Conselho Nacional de Desenvolvimento Cientico e Tecnologico (CNPq) under Grant 304248/2014-2 and Grant 308365/2017-8, in part by the Rede Nacional de Ensino e Pesquisa (RNP), with resources from Ministerio da Ciencia, Tecnologia, Inovacoes e Comunicacoes (MCTIC), through the Radiocommunication Reference Center [Centro de Referencia em Radiocomunicacoes (CRR)] Project of the National Institute of Telecommunications [Instituto Nacional de Telecomunicacoes (INATEL)], Brazil, under Grant 01250.075413/2018-04, and in part by the Ministerio de Economia, Industria y Competitividad of the Spanish Government through the Agencia Estatal de Investigacion (AEI) and the Fondo Europeo de Desarrollo Regional (FEDER) under Project TEC2017-86779-C2-2-R.Dos Anjos, AA.; Rufino-Marins, TR.; Nogueira Da Silva, CR.; Rodrigo Peñarrocha, VM.; Rubio Arjona, L.; Reig, J.; Amaral De Souza, RA.... (2019). Higher Order Statistics in a mmWave Propagation Environment. IEEE Access. 7:103876-103892. https://doi.org/10.1109/ACCESS.2019.2930931S103876103892

A nested loop for simultaneous model topology screening, parameters estimation, and identification of the optimal number of experiments: Application to a Simulated Moving Bed unit

Simulated Moving Bed (SMB) chromatography is a well-known technique for the resolution of several high-value-added compounds. Parameters identification and model topology definition are arduous when one is dealing with complex systems such as a Simulated Moving Bed unit. Moreover, the large number of experiments necessary might be an expansive-long process. Hence, this work proposes a novel methodology for parameter estimation, screening the most suitable topology of the models sink-source (defined by the adsorption isotherm equation) and defining the minimum number of experiments necessary to identify the model. Therefore, a nested loop optimization problem is proposed with three levels considering the three main goals of the work: parameters estimation; topology screening by isotherm definition; minimum number of experiments necessary to yield a precise model. The proposed methodology emulated a real scenario by introducing noise in the data and using a Software-in-the-Loop (SIL) approach. Data reconciliation and uncertainty evaluation add robustness to the parameter estimation adding precision and reliability to the model. The methodology is validated considering experimental data from literature apart from the samples applied for parameter estimation, following a cross-validation. The results corroborate that it is possible to carry out trustworthy parameter estimation directly from an SMB unit with minimal system knowledge

Lipophosphoglycan Polymorphisms Do Not Affect \u3cem\u3eLeishmania amazonensis\u3c/em\u3e Development in the Permissive Vectors \u3cem\u3eLutzomyia migonei\u3c/em\u3e and \u3cem\u3eLutzomyia longipalpis\u3c/em\u3e

Background: Lipophosphoglycan (LPG) is a dominant surface molecule of Leishmaniapromastigotes. Its species-specific polymorphisms are found mainly in the sugars that branch off the conserved Gal(β1,4)Man(α1)-PO4 backbone of repeat units. Leishmania amazonensis is one of the most important species causing human cutaneous leishmaniasis in the New World. Here, we describe LPG intraspecific polymorphisms in two Le. amazonensis reference strains and their role during the development in three sand fly species. Results: Strains isolated from Lutzomyia flaviscutellata (PH8) and from a human patient (Josefa) displayed structural polymorphism in the LPG repeat units, possessing side chains with 1 and 2 β-glucose or 1 to 3 β-galactose, respectively. Both strains successfully infected permissive vectors Lutzomyia longipalpis and Lutzomyia migonei and could colonize their stomodeal valve and differentiate into metacyclic forms. Despite bearing terminal galactose residues on LPG, Josefa could not sustain infection in the restrictive vector Phlebotomus papatasi. Conclusions: LPG polymorphisms did not affect the ability of Le. amazonensis to develop late-stage infections in permissive vectors. However, the non-establishment of infection in Ph. papatasi by Josefa strain suggested other LPG-independent factors in this restrictive vector

Targeted Therapy for Metastatic Renal Carcinoma: An Update

Conventional chemotherapy is associated with poor outcomes in metastatic renal cell carcinoma (RCC). Advances in the understanding of tumor molecular biology and the implementation of new drugs that target these molecular pathways have increased the arsenal against advanced RCC and improved outcomes in these patients. Herein, we briefly describe the latest data on targeted therapies used in the treatment of advanced renal cell carcinoma. Search strategy was performed according to PRISMA guidelines. Abstracts of relevant studies published in PubMed between 2000 and 2014 were analyzed by two authors. Abstracts were selected if they were published in English, data reported was of phase II or III clinical trials, and outcomes followed FDA approval.  If consensus between the two authors was achieved, they were included in the review. Key words used were “target therapy” and “metastatic renal cell carcinoma”. The results of the studies analyzed in this review support the benefits of targeted therapy in metastatic RCC. These include improved progression-free survival, overall survival, and quality of life as well as reduced toxicities compared to immunotherapy. The improvement in outcomes in metastatic RCC makes these drugs a preferred option as a primary treatment for these patients.

Strong Coupling Constant with Flavour Thresholds at Four Loops in the MS-bar Scheme

We present in analytic form the matching conditions for the strong coupling constant alpha_s^(n_f)(mu) at the flavour thresholds to three loops in the modified minimal-subtraction scheme. Taking into account the recently calculated coefficient beta_3 of the Callan-Symanzik beta function of quantum chromodynamics, we thus derive a four-loop formula for alpha_s^(n_f)(mu) together with appropriate relationships between the asymptotic scale parameters Lambda^(n_f) for different numbers of flavours n_f.Comment: 10 pages (Latex), 3 figures (Postscript

Two-loop amplitudes with nested sums: Fermionic contributions to e+ e- --> q qbar g

We present the calculation of the nf-contributions to the two-loop amplitude for e+ e- --> q qbar g and give results for the full one-loop amplitude to order eps^2 in the dimensional regularization parameter. Our results agree with those recently obtained by Garland et al.. The calculation makes extensive use of an efficient method based on nested sums to calculate two-loop integrals with arbitrary powers of the propagators. The use of nested sums leads in a natural way to multiple polylogarithms with simple arguments, which allow a straightforward analytic continuation.Comment: 31 pages, a file "coefficients.h" with the results in FORM format is include

Lipophosphoglycans from \u3cem\u3eLeishmania amazonensis\u3c/em\u3e Strains Display Immunomodulatory Properties via TLR4 and Do Not Affect Sand Fly Infection

The immunomodulatory properties of lipophosphoglycans (LPG) from New World species of Leishmania have been assessed in Leishmania infantum and Leishmania braziliensis, the causative agents of visceral and cutaneous leishmaniasis, respectively. This glycoconjugate is highly polymorphic among species with variation in sugars that branch off the conserved Gal(β1,4)Man(α1)-PO4 backbone of repeat units. Here, the immunomodulatory activity of LPGs from Leishmania amazonensis, the causative agent of diffuse cutaneous leishmaniasis, was evaluated in two strains from Brazil. One strain (PH8) was originally isolated from the sand fly and the other (Josefa) was isolated from a human case. The ability of purified LPGs from both strains was investigated during in vitro interaction with peritoneal murine macrophages and CHO cells and in vivo infection with Lutzomyia migonei. In peritoneal murine macrophages, the LPGs from both strains activated TLR4. Both LPGs equally activate MAPKs and the NF-κB inhibitor p-IκBα, but were not able to translocate NF-κB. In vivo experiments with sand flies showed that both stains were able to sustain infection in L. migonei. A preliminary biochemical analysis indicates intraspecies variation in the LPG sugar moieties. However, they did not result in different activation profiles of the innate immune system. Also those polymorphisms did not affect infectivity to the sand fly

Enhanced role of adenosine A2A receptors in the modulation of LTP in the rat hippocampus upon ageing

Adenosine neuromodulation depends on a balanced activation of inhibitory A1 (A1R) and facilitatory A2A receptors (A2AR). Both A1R and A2AR modulate hippocampal glutamate release and NMDA-dependent long-term potentiation (LTP) but ageing affects the density of both A1R and A2AR. We tested the effects of selective A1R and A2AR antagonists in the modulation of synaptic transmission and plasticity in rat hippocampal slices from three age groups (young adults, 2–3 month; middle-aged adults, 6–8 months; aged, 18–20 months). The selective A2AR antagonist SCH58261 (50 nm) attenuated LTP in all age groups, with a larger effect in aged ()63 ± 7%) than in middle-aged adults ()36 ± 9%) or young adult rats ()36 ± 9%). In contrast, the selective A1R antagonist DPCPX (50 nm) increased LTP magnitude in young adult rats (+42 ± 6%), but failed to affect LTP magnitude in the other age groups. Finally, in the continuous presence of DPCPX, SCH58261 caused a significantly larger inhibition of LTP amplitude in aged ()71 ± 45%) than middle-aged ()28 ± 9%) or young rats ()11 ± 2%). Accordingly, aged rats displayed an increased expression of A2AR mRNA in the hippocampus and a higher number of glutamatergic nerve terminals equipped with A2AR in aged (67 ± 6%) compared with middle-aged (34 ± 7%) and young rats (25 ± 5%). The results show an enhanced A2AR-mediated modulation of LTP in aged rats, in accordance with the age-associated increased expression and density of A2AR in glutamatergic terminals. This age-associated gain of function of A2AR modulating synaptic plasticity may underlie the ability of A2AR antagonists to prevent memory dysfunction in aged animals