Electronic excitations and the tunneling spectra of metallic nanograins

Tunneling-induced electronic excitations in a metallic nanograin are classified in terms of {\em generations}: subspaces of excitations containing a specific number of electron-hole pairs. This yields a hierarchy of populated excited states of the nanograin that strongly depends on (a) the available electronic energy levels; and (b) the ratio between the electronic relaxation rate within the nano-grain and the bottleneck rate for tunneling transitions. To study the response of the electronic energy level structure of the nanograin to the excitations, and its signature in the tunneling spectrum, we propose a microscopic mean-field theory. Two main features emerge when considering an Al nanograin coated with Al oxide: (i) The electronic energy response fluctuates strongly in the presence of disorder, from level to level and excitation to excitation. Such fluctuations produce a dramatic sample dependence of the tunneling spectra. On the other hand, for excitations that are energetically accessible at low applied bias voltages, the magnitude of the response, reflected in the renormalization of the single-electron energy levels, is smaller than the average spacing between energy levels. (ii) If the tunneling and electronic relaxation time scales are such as to admit a significant non-equilibrium population of the excited nanoparticle states, it should be possible to realize much higher spectral densities of resonances than have been observed to date in such devices. These resonances arise from tunneling into ground-state and excited electronic energy levels, as well as from charge fluctuations present during tunneling.Comment: Submitted to the Physical Review

Radioimmunotherapy of B-cell lymphoma with radiolabelled anti-CD20 monoclonal antibodies

CD20 has proven to be an excellent target for the treatment of B-cell lymphoma, first for the chimeric monoclonal antibody rituximab (Rituxan™), and more recently for the radiolabelled antibodies Y-90 ibritumomab tiuxetan (Zevalin™) and I-131 tositumomab (Bexxar™). Radiation therapy effects are due to beta emissions with path lengths of 1–5 mm; gamma radiation emitted by I-131 is the only radiation safety issue for either product. Dose-limiting toxicity for both radiolabelled antibodies is reversible bone marrow suppression. They produce response rates of 70%–90% in low-grade and follicular lymphoma and 40%–50% in transformed low-grade or intermediate-grade lymphomas. Both products produce higher response rates than related unlabelled antibodies, and both are highly active in patients who are relatively resistant to rituximab-based therapy. Median duration of response to a single course of treatment is about 1 year with complete remission rates that last 2 years or longer in about 25% of patients. Clinical trials suggest that anti- CD20 radioimmunotherapy is superior to total body irradiation in patients undergoing stem cell supported therapy for B-cell lymphoma, and that it is a safe and efficacious modality when used as consolidation therapy following chemotherapy. Among cytotoxic treatment options, current evidence suggests that one course of anti-CD20 radioimmunotherapy is as efficacious as six to eight cycles of combination chemotherapy. A major question that persists is how effective these agents are in the setting of rituximab- refractory lymphoma. These products have been underutilised because of the complexity of treatment coordination and concerns regarding reimbursement

Reproductive cycle of the brachiopod Terebratulina retusa on the west coast of Scotland

The reproductive cycles of two populations of the Recent articulate brachiopodTerebratulina retusa (Linnaeus) are described, based on samples taken between October 1985 and October 1986. Stereological analysis of the gonads revealed a single synchronised spawning event between late November and the end of January in the Firth of Lorn. In a second population, in Loch Fyne, spawning took place repeatedly throughout the spring and summer, with greatest spawning activity occurring in the late autumn.T. retusa from Loch Fyne were approximately three times more fecund than those from the Firth of Lorn. Productivity in the Clyde Sea area is approximately five times higher than in Firth of Lorn and higher fecundities and spawning frequencies of the Loch Fyne population are attributed, in part, to greater food availability. The initiation of gametogenesis appears to be mediated by the mobilisation of reserves stored in the outer mantle epithelium during the winter. Primary productivity increases dramatically in the spring and gametogenesis shows a corresponding increas

Functional morphology of the gonads of the articulate brachiopod Terebratulina retusa

The reproductive anatomy, and ultrastructural features of the gonads of the articulate brachiopodTerebratulina retusa (Linnaeus), are documented based on collections made between October 1985 and October 1986 from the Firth of Lorn, west coast of Scotland. This species is dioecious, and maturity is achieved in both sexes at shell lengths greater than ~5.5 mm. There is no obvious external sexual dimorphism except for slight differences in the coloration of the gonads; testes are white/cream, ovaries are yellow/orange. The gonads occur as four palmate lobes, a pair in each valve. Gonads are formed within a mantle sinus (vascula genitalia), which is an anterior extension of the coelom, that opens posteriorly into the visceral cavity and to the exterior via a pair of metanephridia. The latter serve as gonoducts during spawning. Gametes are borne on genital lamellae formed from a reticulate lattice of connective tissue. The lamellae are an extension of the ileoparietal band and are fused along one margin to the inner mantle membrane. Developing oocytes are closely affixed to the genital lamellae and originate from a pool of proliferating germ cells at its base. Vitellogenic oocytes that are at an advanced stage are released from the genital lamellae, but are retained within thevascula genitalia. Liberated oocytes continue to accumulate yolk and eventually occlude thevascula genitalia, before being spawned. Coelomocytes were identified within the gonads. In spent females these cells appear to be phagocytic and involved in the resorption of necrotic material, while in the male they may serve as nutritive cell

Oogenesis in the articulate brachiopod Terebratulina retusa

A detailed ultrastructural description of oogenesis is presented for the articulate brachiopodTerebratulina retusa (Linnaeus), based on collections made between October 1985 and October 1986 from the Firth of Lorn, west coast of Scotland. Oogenesis has been divided into six stages, defined according to ultrastructural changes, which are thought to be important steps in the process of vitellogenesis. Special attention has been given to the possible mechanisms involved in the acquisition and assimilation of nutrients within the differentiating oocyte. Each vitellogenic oocyte is contained within a follicular envelope which is attached to a genital lamella. As maturation proceeds, accessory cells proliferate within the follicular envelope. A variety of intra-accessory cell and oocyte/accessory cell communications were identified. The process of elaboration of the oolemma is reported in detail. Lipid was identified as the major nutrient reserve of the oocyte. Late mature oocytes measure ~130 µm in diameter when spawned. The process of oosorption is also documente

Swimming in the Antarctic scallop Adamussium colbecki: analysis of in situ video recordings

Swimming activity of the Antarctic scallop at a temperature of c. - 1.4" C was analysed using in situ video recordings obtained from a remotely operated vehicle (ROV) in Terra Nova Bay, Ross Sea. Data are presented on swimming trajectories, distance travelled and velocity during a swimming bout, adduction frequency, shell gape angle, and the angular opening and closing velocities of shell. This scallop is an effective swimmer although swimming bouts in response to the ROV were generally short, consisting of 2-5 adduction cycles in the take-off phase followed by 1-4 (exceptionally 14) adductions during level swimming. The maximum velocity during each adduction cycle ranged from 19.443.1 cm s-' and the mean velocity during a swimming bout from 12.0-23.5 cm s-I. Each adduction cycle consists of opening, closing and glide phases of approximately equal duration. Adduction frequency during swimming averaged 1.5 adductions s-I

Temperature and starvation effects on the metabolism of the brachiopod, Terebratulina retusa (L.)

Oxygen consumption and ammonia excretion rates were assessed for Terebratulina retusa (L.) held under 3 different regimes of temperature and food availability. These were: 5.6^C, no food (cold, starved); 5.8^C, food present (cold, fed) and 10.7ˆC food present (warm, fed), which simulated winter conditions, summer conditions and an intermediate treatment. Regressions of oxygen consumption on ash-free dry weight (AFDW) had slopes which were not significantly different from each other and ranged from 0.953 to 0.999. A common slope of 0.976 was calculated and intercepts based on the common slope used to compare oxygen consumption in each treatment. The rise from cold, starved conditions to warm, fed was 24.5 per cent and this was significant (P < 0.05). Other differences were not significant (P > 0.05) but the cold, fed result was 12.6 per cent higher than cold, starved. Therefore feeding and temperature probably account for equivalent proportions of the rise in metabolism from winter to summer. Ammonia production data were much more variable. Excretion rates of a 50 mg AFDW individual (in ng-at NH<sub>3</sub>-N.h-¹) were as follows: cold, starved: 30.2 cold, fed: 7.1; and warm, fed: 22.9. Oxygen to nitrogen (O:N) ratios reflected these results. Mean O:N ratios were: cold, starved: 8.0; cold, fed: 42.4; warm, fed: 16.3. This shows that the simulated winter group relied heavily on protein to fuel their metabolism, the simulated summer group were less dependent on protein and the intermediate group probably used lipids and carbohydrates to fuel metabolic demands. This possibly reflected a trade off between food supply and increased metabolism from treatment to treatment, demonstrating a flexibility which could have been a contributing factor in the ecological tolerance and geological longevity of some brachiopod

Physiological constraints on living and fossil brachiopods

Ash-free-dry-weight determinations for a representative range of living brachiopod genera have revealed that a consistently high proportion of total organic mass is contained within the shell, partly as the organic matrix for biomineralisation and partly as minute extensions of the mantle tissues (caeca) housed within hollow endopunctae permeating the shell. On average 40% to 50% of the total organic mass of both articulate and inarticulate brachiopods is situated within the shell. This is true even for a rhynchonellid brachiopod which does not possess endopunctae, but which has a more dense protein matrix in its shell. The effectively hidden constituent of brachiopod tissue mass which is included in this component has often been overlooked, and as a result total metabolic tissue mass has been underestimated. This throws into question some previous interpretations of brachiopod respiratory and metabolic data. The oxygen consumption rates of several living brachiopods have been measured, and when respiring tissue in caeca in the shell is taken into consideration, it is clear that brachiopod metabolic rates are low when compared with other marine invertebrates (e.g. between 10% and 50% of the oxygen uptake of comparable gastropods and bivalve molluscs held in similar conditions). This low rate cannot be attributed to a slower pumping rate by the brachiopod lophophore, as has been suggested, because the rate of water movement is comparable to that across the bivalve gill. Nitrogen excretion rates have also been measured for a few living brachiopods, allowing a comparison with rates of oxygen consumption and providing an indication of the metabolic substrates used. These data on oxygen: nitrogen ratios suggest that one Antarctic brachiopod utilises exclusively protein as a metabolic substrate, while a temperate latitude species uses mainly protein during winter but lipids and carbohydrates during summer months. Histological observations, particularly of Terebratulina retusa from temperate waters, show that a specialised tissue layer in the brachiopod outer mantle epithelium proximal to the shell may be the site of storage of the protein that is metabolised during winter, and of carbohydrate mobilised during gonadal development in summer. The caeca have also been suggested as sites of storage of metabolites, and the possible relationships between these areas of mantle are discussed. It seems that the ability to store nutrients in the mantle, combined with flexibility of substrate utilisation and an inherently low metabolic rate, have been important factors in brachiopod evolution