Flow through very porous screens

Flow through and around screens with small resistance coefficient were analyzed. Both steady and oscillatory flows are considered, however, the case of a screen normal to the flow is treated. At second order in the asymptotic expansion the steady flow normal to the screen is nonuniform along the screen, due to components induced by the wake and by tangential drag. The third order pressure drop is nonuniform and the wake contains distributed vorticity, in addition to the vortex sheet along its boundary. The unsteady drag coefficient is found as a function of frequency

Persistent activation of steroidogenesis in adrenocortical cells by photoaffinity labeling of corticotropin receptors

Photolysis of rat adrenocortical cells in the presence of the photoreactive derivative [(2-nitro-5-azidophenylsulfenyl)Trp9]-adrenocorticotropic hormone (2,5-NAPS-ACTH) at 24°C resulted in persistent activation of corticosterone production. The basal rate of steroidogenesis became maximal when photolysis was performed at 24°C but remained the same as that of control cells when irradiation was performed at 0°C. No increase in basal rate was observed with dark controls or cells photolyzed with [(2,4-dinitrophenylsulfenyl)Trp9]ACTH, a photoresistant analog of the hormone. Prephotolyzed 2,5-NAPS-ACTH failed to induce persistent activation. Both ACTH and 2,4-(dinitrophenylsulfenyl)Trp9-ACTH blocked the photo-induced activation of steroidogenesis elicited by 2,5-NAPS-ACTH. Under photolysis conditions which caused the basal rate of steroidogenesis to become maximal, a 3-fold increase in the basal rate of cAMP formation was observed

Analytical modeling of circuit aerodynamics in the new NASA Lewis wind tunnel

Rehabilitation and extention of the capability of the altitude wind tunnel (AWT) was analyzed. The analytical modeling program involves the use of advanced axisymmetric and three dimensional viscous analyses to compute the flow through the various AWT components. Results for the analytical modeling of the high speed leg aerodynamics are presented; these include: an evaluation of the flow quality at the entrance to the test section, an investigation of the effects of test section bleed for different model blockages, and an examination of three dimensional effects in the diffuser due to reentry flow and due to the change in cross sectional shape of the exhaust scoop

Phase diagram of an exactly solvable t-J ladder model

We study a system of one-dimensional t-J models coupled to a ladder system. A special choice of the interaction between neighbouring rungs leads to an integrable model with supersymmetry, which is broken by the presence of rung interactions. We analyze the spectrum of low-lying excitations and ground state phase diagram at zero temperature.Comment: LaTeX, 8 pp. incl. 1 figur

Phase diagram of the su(8) quantum spin tube

We calculate the phase diagram of an integrable anisotropic 3-leg quantum spin tube connected to the su(8) algebra. We find several quantum phase transitions for antiferromagnetic rung couplings. Their locations are calculated exactly from the Bethe Ansatz solution and we discuss the nature of each of the different phases.Comment: 10 pages, RevTeX, 1 postscript figur

There and back again: migration in freshwater fishes

Animal migration is an amazing phenomenon that has fascinated humans for long. Many freshwater fishes also show remarkable migrations, whereof the spectacular mass migrations of salmonids from the spawning streams are the most well known and well studied. However, recent studies have shown that migration occurs in a range of freshwater fish taxa from many different habitats. In this review we focus on the causes and consequences of migration in freshwater fishes. We start with an introduction of concepts and categories of migration, and then address the evolutionary causes that drive individuals to make these migratory journeys. The basis for the decision of an individual fish to migrate or stay resident is an evaluation of the costs and benefits of different strategies to maximize its lifetime reproductive effort. We provide examples by discussing our own work on the causes behind seasonal migration in a cyprinid fish, roach (Rutilus rutilus (L., 1758)), within this framework. We then highlight different adaptations that allow fish to migrate over sometimes vast journeys across space, including capacity for orientation, osmoregulation, and efficient energy expenditure. Following this we consider the consequences of migration in freshwater fish from ecological, evolutionary, and conservation perspectives, and finally, we detail some of the recent developments in the methodologies used to collect data on fish migration and how these could be used in future research

Deciphering interplay between Salmonella invasion effectors

Bacterial pathogens have evolved a specialized type III secretion system (T3SS) to translocate virulence effector proteins directly into eukaryotic target cells. Salmonellae deploy effectors that trigger localized actin reorganization to force their own entry into non-phagocytic host cells. Six effectors (SipC, SipA, SopE/2, SopB, SptP) can individually manipulate actin dynamics at the plasma membrane, which acts as a ‘signaling hub’ during Salmonella invasion. The extent of crosstalk between these spatially coincident effectors remains unknown. Here we describe trans and cis binary entry effector interplay (BENEFIT) screens that systematically examine functional associations between effectors following their delivery into the host cell. The results reveal extensive ordered synergistic and antagonistic relationships and their relative potency, and illuminate an unexpectedly sophisticated signaling network evolved through longstanding pathogen–host interaction

Note on the thermodynamic Bethe Ansatz approach to the quantum phase diagram of the strong coupling ladder compounds

We investigate the low-temperature phase diagram of the exactly solved su(4) two-leg spin ladder as a function of the rung coupling $J_{\perp}$ and magnetic field $H$ by means of the thermodynamic Bethe Ansatz (TBA). In the absence of a magnetic field the model exhibits three quantum phases, while in the presence of a strong magnetic field there is no singlet ground state for ferromagnetic rung coupling. For antiferromagnetic rung coupling, there is a gapped phase in the regime H H_{c2} and a Luttinger liquid magnetic phase in the regime H_{c1} < H < H_{c2}. The critical behaviour derived using the TBA is consistent with the existing experimental, numerical and perturbative results for the strong coupling ladder compounds. This includes the spin excitation gap and the critical fields H_{c1} and H_{c2}, which are in excellent agreement with the experimental values for the known strong coupling ladder compounds (5IAP)_2CuBr_4 2H_2 O, Cu_2(C_5 H_{12} N_2)_2 Cl_4 and (C_5 H_{12} N)_2 CuBr_4. In addition we predict the spin gap $\Delta \approx J_{\perp}-{1/2}J_{\parallel}$ for the weak coupling compounds with $J_{\perp} \sim J_{\parallel}$, such as (VO)_2 P_2 O_7, and also show that the gap opens for arbitrary $J_{\perp}/ J_{\parallel}$.Comment: 10 pages, 3 figure