Nuove specie per l'acquacoltura: tecniche di produzione di novellame di Sardina pilchardus

Il progetto all’interno del quale si è inserita l' attività "Sperimentare in acquacoltura il novellame di Sardina pilchardus" è il Progetto Ritmare (La Ricerca Italiana per il Mare). Il progetto Ritmare è un progetto strategico per la ricerca sul mare in Italia, che vuole coniugare le risorse ambientali del mare con l’uso connesso alle attività produttive e allo sfruttamento energetico delle sue risorse, sviluppando tecnologie ed innovazione e, al tempo stesso, promuovendone la sua conoscenza e il rispetto. In tale contesto il progetto mira a sperimentare in acquacoltura il novellame di sardina, prodotto agroalimentare tradizionalmente consumato e molto richiesto nei paesi rivieraschi del Mediterraneo. ll novellame per anni è stato pescato in modo puntuale ma per la bassissima sostenibilità e per l’impatto sugli stock adulti, la comunità europea ne ha deciso la sospensione. Il progetto vuole tentare di reintegrare il prodotto sul mercato attraverso una produzione sostenibile, evitando la perdita culturale. Saranno indagate le caratteristiche organolettiche del prodotto per promuoverne il consumo e verificate le ricadute industriali attraverso la realizzazione di un Business plan.

Programma nazionale Italiano per la raccolta di dati alieutici modulo: CAMP-BIOL 2003 Rapporto finale sulle specie demersali nello Stretto di Sicilia (Sub Area Geografica 16; Mar Mediterraneo)

Il modulo (CAMP-BIOL) del programma nazionale Italiano per la raccolta dei dati alieutici, in applicazione della normativa prevista dai regolamenti comunitari n°1534/2000 e 1639/2001, si propone di campionare pesci, molluschi e crostacei sfruttati dalla pesca commerciale con l’obiettivo di acquisire informazioni riguardanti le caratteristiche biologiche del pescato.

Programma nazionale Italiano per la raccolta di dati alieutici modulo CAMP-BIOL 2004 Rapporto finale sulle specie demersali nello Stretto di Sicilia (Sub Area Geografica 16; Mar Mediterraneo)

Il modulo (CAMP-BIOL) del programma nazionale Italiano (PNI), per la raccolta di dati alieutici, in applicazione della normativa prevista dai regolamenti comunitari n°1534/2000 e 1639/2001, ha l’obiettivo di studiare pesci, molluschi e crostacei sbarcati dalla pesca commerciale per acquisire informazioni riguardanti le caratteristiche biologiche del pescato. Tali informazioni, come lo scorso anno, riguardano la composizione in lunghezza e/o età del pescato italiano per le principali risorse da pesca (piccoli pelagici, grandi pelagici e demersali) e per le diverse tipologie di pesca che costituiscono la flotta peschereccia italiana (strascico, circuizione e attrezzi fissi).

Monitoraggio delle risorse ittiche e della pesca: indagine sugli spostamenti di specie marine di interesse commerciale e conservazionistico

Il monitoraggio degli spostamenti degli organismi marini è un importante strumento per la comprensione della biologia delle specie ma anche per la conservazione e la tutela degli stock intesi come risorsa. Nel caso dell'applicazione su specie che vivono all'interno di Aree Marine Protette, queste tecniche consentono di verificare l'efficacia della protezione. Questo studio riporta l'applicazione di tecniche di telemetria ultrasonica all'aragosta comune (P. elephas) nell'AMP di Isola delle Femmine. Gli individui catturati all'interno dell'AMP ed ivi rilasciati hanno mostrato uno spiccato homing ed un buon livello di fedeltà al sito. Lo studio inoltre è servito a denunciare lo stato attuale di scarsa protezione e suggerisce una riperimetrazione dei confini dell'AMP.

Trattamento plasma assistito di acqua con una sorgente Dielectric Barrier Discharge (DBD): analisi delle specie reattive prodotte e potere battericida

La proliferazione di batteri in liquido è una problematica che riguarda anche le acque di fiumi e mari. In questo progetto di tesi sperimentale si indagherà un trattamento plasma assistito diretto di acqua sintetica riprodotta in laboratorio con l’obiettivo di ottenere un effetto battericida sul liquido contaminato. L’acqua trattata verrà analizzata chimicamente, in particolare si andranno a misurare i TRO (Total Residual Oxidant, composti dell’ossigeno derivanti dalla parziale ozonizzazione dell’acqua) che dovranno essere presenti in quantità minori di 0,1 mg/l. Il dispositivo utilizzato per i test biologici è una sorgente di tipologia DBD (Dielectric Barrier Discharge) indiretto. Gli elettrodi della sorgente sono separati dal solo strato di materiale dielettrico e uno di questi è composto da una rete metallica in acciaio inossidabile. Il plasma si forma tra le maglie della rete e induce la formazione di specie reattive, radiazioni UV, particelle cariche, campi elettromagnetici e calore. Ciò che raggiunge la soluzione contaminata è l’afterglow del plasma, ovvero tutte le specie reattive a lunga vita prodotte dalla ionizzazione dell’aria e dalle radiazioni UV. La sorgente è stata dapprima caratterizzata elettricamente studiando le forme d’onda di tensione e corrente a determinate condizioni operative. Il liquido da trattare è contaminato con il batterio Escherichia coli. è emerso che in tutti i casi testati i livelli degli ossidanti sono entro il limite prestabilito di 0,1 mg/l. Il trattamento plasma in soli 10 secondi è responsabile di una decontaminazione parziale del batterio E. coli. Da ulteriori studi si potranno trovare delle condizioni tali da inattivare totalmente la carica batterica presente date le grandi potenzialità di questo trattamento.

Use of hydrotalcites for the removal of toxic anions from aqueous solutions

The removal of toxic anions has been achieved using hydrotalcite via two methods: (1) coprecipitation and (2) thermal activation. Hydrotalcite formed via the coprecipitation method, using solutions containing arsenate and vanadate up to pH 10, are able to remove more than 95% of the toxic anions (0.2 M) from solution. The removal of toxic anions in solutions with a pH of >10 reduces the removal uptake percentage to 75%. Raman spectroscopy observed multiple A1 stretching modes of V−O and As−O at 930 and 810 cm−1, assigned to vanadate and arsenate, respectively. Analysis of the intensity and position of the A1 stretching modes helped to identify the vanadate and arsenate specie intercalated into the hydrotalcite structure. It has been determined that 3:1 hydrotalcite structure predominantly intercalate anions into the interlayer region, while the 2:1 and 4:1 hydrotalcite structures shows a large portion of anions being removed from solution by adsorption processes. Treatment of carbonate solutions (0.2 M) containing arsenate and vanadate (0.2 M) three times with thermally activated hydrotalcite has been shown to remove 76% and 81% of the toxic anions, respectively. Thermally activated hydrotalcite with a Mg:Al ratio of 2:1, 3:1, and 4:1 have all been shown to remove 95% of arsenate and vanadate (25 ppm). At increased concentrations of arsenate and vanadate, the removal uptake percentage decreased significantly, except for the 4:1 thermally activated hydrotalcite. Thermally activated Bayer hydrotalcite has also been shown to be highly effective in the removal of arsenate and vanadate. The thermal activation of the solid residue component (red mud) removes 30% of anions from solution (100 ppm of both anions), while seawater-neutralized red mud removes 70%. The formation of hydrotalcite during the seawater neutralization process removes anions via two mechanisms, rather than one observed for thermally activated red mud.

Preliminary characterisation of the surface of cartilage following exposure to saturated and unsaturated synthetic lipids

Articular cartilage is covered by a microscopic structure known as surface amorphous layer. This surface structure is often the first victim of attack during cartilage degeneration, thereby resulting in a gross impairment in cartilage function such as lubrication and load bearing. We hypothesize that incubation of degraded cartilage in solutions of different species of synthetic surface active phospholipids (saturated and unsaturated species) can remodel this lost surface structure. To test this hypothesis, the structural configuration of the surface of articular cartilage was studied and characterised with the lipid filled surface amorphous layer intact using the AFM. The results were then compared with those obtained following a systematic removal (delipidization) and replacement (relipidization) of this layer. Our results show that the unsaturated surfactant partially restored the lost surface amorphous layer while the saturated surfactant specie settled on the surface due to its poor solubility in aqueous solution.

Ion-assisted functional monolayer coating of nanorod arrays in hydrogen plasmas

Uniformity of postprocessing of large-area, dense nanostructure arrays is currently one of the greatest challenges in nanoscience and nanofabrication. One of the major issues is to achieve a high level of control in specie fluxes to specific surface areas of the nanostructures. As suggested by the numerical experiments in this work, this goal can be achieved by manipulating microscopic ion fluxes by varying the plasma sheath and nanorod array parameters. The dynamics of ion-assisted deposition of functional monolayer coatings onto two-dimensional carbon nanorod arrays in a hydrogen plasma is simulated by using a multiscale hybrid numerical simulation. The numerical results show evidence of a strong correlation between the aspect ratios and nanopattern positioning of the nanorods, plasma sheath width, and densities and distributions of microscopic ion fluxes. When the spacing between the nanorods and/or their aspect ratios are larger, and/or the plasma sheath is wider, the density of microscopic ion current flowing to each of the individual nanorods increases, thus reducing the time required to apply a functional monolayer coating down to 11 s for a 7-μm-wide sheath, and to 5 s for a 50-μm-wide sheath. The computed monolayer coating development time is consistent with previous experimental reports on plasma-assisted functionalization of related carbon nanostructures [B. N. Khare et al., Appl. Phys. Lett. 81, 5237 (2002)]. The results are generic in that they can be applied to a broader range of plasma-based processes and nanostructures, and contribute to the development of deterministic strategies of postprocessing and functionalization of various nanoarrays for nanoelectronic, biomedical, and other emerging applications.

Evaluation of rumen fatty acid hydrogenation intermediates and differences in bacterial communities after feeding wheat- or corn-based dried distillers grains to feedlot cattle

The effect of partially replacing rolled barley (86.6% of control diet) with 20% wheat dried distillers grains plus solubles (DDGS), 40% wheat DDGS, 20% corn DDGS, or 40% corn DDGS (dietary DM basis) on rumen fluid fatty acid (FA) composition and some rumen bacterial communities was evaluated using 100 steers (20 per treatment). Wheat DDGS increased the 11t-to 10t-18:1 ratio (P < 0.05) in rumen fluid and there was evidence that the conversion of trans-18:1 to 18:0 was reduced in the control and wheat DDGS diets but not in the corn DDGS diet. Bacterial community profiles obtained using denaturing gradient gel electrophoresis and evaluated by Pearson correlation similarity matrices were not consistent for diet and, therefore, these could not be linked to different specific rumen FA. This inconsistency may be related to the nature of diets fed (dominant effect of barley), limited change in dietary composition as the result of DDGS inclusion, large animal-to-animal variation, and possibly additional stress as a result of transport just before slaughter. Ruminal densities of a key fiber-digesting bacteria specie that produces 11t-18:1 from linoleic and linolenic acids (Butyrivibrio fibrisolvens), and a lactate producer originally thought responsible for production of 10t, 12c-18:2 (Megasphaera elsdenii) were not influenced by diet (P > 0.05).

Influence of fuel hydrogen fraction on syngas fueled SI engine: Fuel thermo-physical property analysis and in-cylinder experimental investigations

Hydrogen, either in pure form or as a gaseous fuel mixture specie enhances the fuel conversion efficiency and reduce emissions in an internal combustion engine. This is due to the reduction in combustion duration attributed to higher laminar flame speeds. Hydrogen is also expected to increase the engine convective heat flux, attributed (directly or indirectly) to parameters like higher adiabatic flame temperature, laminar flame speed, thermal conductivity and diffusivity and lower flame quenching distance. These factors (adversely) affect the thermo-kinematic response and offset some of the benefits. The current work addresses the influence of mixture hydrogen fraction in syngas on the engine energy balance and the thermo-kinematic response for close to stoichiometric operating conditions. Four different bio-derived syngas compositions with fuel calorific value varying from 3.14 MJ/kg to 7.55 MJ/kg and air fuel mixture hydrogen fraction varying from 7.1% to 14.2% by volume are used. The analysis comprises of (a) use of chemical kinetics simulation package CHEMKIN for quantifying the thermo-physical properties (b) 0-D model for engine in-cylinder analysis and (c) in-cylinder investigations on a two-cylinder engine in open loop cooling mode for quantifying the thermo-kinematic response and engine energy balance. With lower adiabatic flame temperature for Syngas, the in-cylinder heat transfer analysis suggests that temperature has little effect in terms of increasing the heat flux. For typical engine like conditions (700 K and 25 bar at CR of 10), the laminar flame speed for syngas exceeds that of methane (55.5 cm/s) beyond mixture hydrogen fraction of 11% and is attributed to the increase in H based radicals. This leads to a reduction in the effective Lewis number and laminar flame thickness, potentially inducing flame instability and cellularity. Use of a thermodynamic model to assess the isolated influence of thermal conductivity and diffusivity on heat flux suggests an increase in the peak heat flux between 2% and 15% for the lowest (0.420 MW/m(2)) and highest (0.480 MW/m(2)) hydrogen containing syngas over methane (0.415 MW/m(2)) fueled operation. Experimental investigations indicate the engine cooling load for syngas fueled engine is higher by about 7% and 12% as compared to methane fueled operation; the losses are seen to increase with increasing mixture hydrogen fraction. Increase in the gas to electricity efficiency is observed from 18% to 24% as the mixture hydrogen fraction increases from 7.1% to 9.5%. Further increase in mixture hydrogen fraction to 14.2% results in the reduction of efficiency to 23%; argued due to the changes in the initial and terminal stages of combustion. On doubling of mixture hydrogen fraction, the flame kernel development and fast burn phase duration decrease by about 7% and 10% respectively and the terminal combustion duration, corresponding to 90%-98% mass burn, increases by about 23%. This increase in combustion duration arises from the cooling of the near wall mixture in the boundary layer attributed to the presence of hydrogen. The enhancement in engine cooling load and subsequent reduction in the brake thermal efficiency with increasing hydrogen fraction is evident from the engine energy balance along with the cumulative heat release profiles. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Anima, mente, corpo e inmortalità : la sfida del naturalismo

Resumen: Il saggio esamina il rapporto anima, mente, corpo alla luce delle sfide del nuovo naturalismo che molto spesso incorpora un secco riduzionismo ed un’opzione materialistica. Questa risulta un apriori, non l’esito di un argomento: J. Searle la chiama “la religione del nostro tempo”. Vengono poi esaminati l’attuale oblio dell’anima, la riduzione del suo tema al mind-body problem, la qualità della tesi ilemorfica, illustrata in specie attraverso le soluzioni dell’Aquinate, l’equivoco del dualismo cartesiano. Chiude il saggio uno sguardo sulla questione dell’immortalità dell’anima.

Mussel Community Studies [Year Two].

The communities associated with Mytilus californianus (mussel) beds from eleven geographic localities in Southern California were examined. The localities included four mainland sites - Government Point, Goleta Point, Corona del Mar and San Diego; and seven offshore islands including - San Miguel Island, Santa Rosa Island, Santa Cruz Island, Santa Barbara Island, Santa Catalina Island, San Nicholas Island and San Clemente Island. This geographic coverage. was much more complete than the previous year (1975-1976 program). However, it is still less than ideal. In particular a single island collection locality may not be representative of an entire island. Therefore greater geographic coverage of the islands is recommended for the future. In general, the 1500 cm2 sample size adopted during the 1975-1976 program proved adequate for sampling most of the structurally diverse mussel beds this year. This sample size supplied information on the characteristic and abundant species inhabiting a particular mussel bed, and provided data which was well suited to intersite community comparisons. This sample size was too small in several instances to include the rarer, less abundant species. The mussel communities from all localities contributed to the master species list which contained conservatively 481 species of animals and 63 specie s of algae. The most diverse collections came from Santa Cruz Island and Corona del Mar, and these areas contained 120 and 119 species respectively. The lowest diversity was recorded for the mussel beds from Goleta Point: which contained 57 species. Mussel community samples were collected from upper and lower intertidal areas occupied by the mussel beds within a locality. In general, community differences both in composition and abundance were associated with these collections. (PDF contains 158 pages)

Ecologia de Astyanax taeniatus na Bacia do Rio Mato Grosso, Saquarema - RJ: Dieta, uso do micro-hábitat e uma breve análise comportamental

Neste trabalho tivemos como objetivo caracterizar a dieta, uso do habitat e padrões comportamentais de Astyanax taeniatus da bacia do Rio Mato Grosso, que encontra-se na porção leste do Estado do Rio de Janeiro (22 52 S; 42 40 W e 22 53 S; 42 34 W). Para a análise da dieta, os exemplares foram coletados bimestralmente entre março de 2006 e janeiro de 2007 em três localidades que diferiram pelas variáveis físicas. As observações de uso dos recursos do habitat foram realizadas por observação subaquática, na posição focal dos exemplares avistados, enquanto a quantificação da disponibilidade foi realizada em 50 quadrats de 20x20cm (400cm2) ao longo dos mesmos 50m onde foi realizada a observação sub-aquática. A análise do conteúdo estomacal de 651 exemplares foi realizada sob microscópio estereoscópico de acordo com métodos qualitativos e quantitativos (Freqüência de Ocorrência e Volumétrica). A participação relativa de cada item registrado nos estômagos em relação à totalidade da dieta foi analisada através do Índice Alimentar (IAi). Para verificar possíveis diferenças entre as proporções dos itens de origem animal e vegetal, autóctone e alóctone, os valores proporcionais foram testados pelo 2 de contingência. A partir dos dados de comprimento padrão e comprimento do intestino, foi calculado o valor do quociente intestinal. Os itens de origem vegetal tiveram maior contribuição na dieta da espécie para as localidades com maior altitude, enquanto os itens animais tiveram maior contribuição na localidade baixa. A diferença na contribuição dos itens de origem autóctone e alóctone também foi significativa. Na dieta de jovens e adultos, houve diferença significativa na contribuição de itens de origem vegetal e animal somente na localidade mais alta, onde os adultos consumiram maior quantidade de matéria vegetal. Os valores médios de quociente intestinal em jovens e adultos foram significativamente diferentes nas localidades de maior altitude, com valores maiores para indivíduos adultos. Observamos 52% dos indivíduos em profundidades entre 30 e 45 cm, 72% em áreas de rápido, 72% em velocidades entre 0 e 0,5km/h, 66% encontravam-se distantes da margem entre 40 e 120 cm, 37,6% em substrato do tipo areia e 34,4% em substrato do tipo pedra. De todos os padrões comportamentais observados, aquele que mais se destacou foi o forrageamento, onde 70,91% dos indivíduos estavam forrageando no meio da coluna dágua. Os resultados da dieta reforçam a idéia de as espécies de Astyanax têm hábito alimentar onívoro e oportunista, onde a espécie alimentou-se dos recursos disponíveis no ambiente evidenciando sua alta plasticidade alimentar ao longo do riacho. Espécies do gênero Astyanax são consideradas generalistas em relação ao uso do habitat e altamente ativas, corroborando com os resultados do presente estudo.

Quantificação de metais (Al, Fe, Mn, Pb, Zn e Cu) nos sedimentos do sistema estuarino das Ilhas de Tinharé-Boipeba (Bahia - Brasil)

O sistema estuarino das Ilhas de Tinharé-Boipeba está inserido na região do Baixo Sul baiano (Bahia Brasil), costa nordeste brasileira, e conectam-se com o oceano através de três saídas principais, Morro de São Paulo, Boipeba e Barra dos Carvalhos. Informações relacionadas à presença de metais no sedimento são quase inexistentes para a região. Nestes estuários foram coletadas 40 amostras de sedimento, onde analisou-se a concentração de metais (Al, Cu, Fe, Mn, Pb e Zn) através da extração com água-régia, segundo o protocolo do material de referência BCR-701 (RAURET et al., 2001). Baixas concentrações de metais foram registradas nas proximidades das saídas para o mar e no Canal de Garapuá e Rio Grande. Altas concentrações, porém praticamente dentro dos valores de referência na CONAMA 344/04, foram registradas no Rio Una, na maior parte do Rio Cairu, Rio das Almas, em quase todas as estações, no braço leste do Rio Cairu e na porção intermediária do Rio dos Patos. As concentrações dos metais (mg.kg1) apresentaram valores entre os seguintes intervalos, Al (3,57 x 104 a 3,19 x 102), Cu (1,02 x 102 a 0,35), Fe (4,33 x 104 a 2,05 x 102), Mn (1,44 x 103 a 2,73), Pb (6,67 x 101 a 2,66) e Zn (5,08 x 102 a 3,18). Através da análise estatística ACP (Análise dos Componentes Principais) e dos gráficos de correlação entre a granulometria do sedimento (areia, silte e argila) e os metais, observou-se maiores concentrações de metais com o aumento do percentual de silte e diminuição do percentual de areia. Também se identificou uma forte correlação entre a ocorrência do fósforo e a presença de metais. Acredita-se que a principal espécie química em questão seja o fosfato (PO43 ou P2O5) que é uma base dura, onde a ligação com os metais se dá pelo oxigênio, sendo o caráter iônico relevante. Não foi identificada uma correlação entre a presença de metais e a argila, fato atribuído ao baixo teor dessa granulometria para todas as amostras do estudo e a composição da argila desses estuários

I. Electron spin relaxation studies of manganese(II) complexes in acetonitrile. II. Nuclear spin relaxation studies of bromine in tetrabromomanganese(II) in acetonitrile

Magnetic resonance techniques have given us a powerful means for investigating dynamical processes in gases, liquids and solids. Dynamical effects manifest themselves in both resonance line shifts and linewidths, and, accordingly, require detailed analyses to extract desired information. The success of a magnetic resonance experiment depends critically on relaxation mechanisms to maintain thermal equilibrium between spin states. Consequently, there must be an interaction between the excited spin states and their immediate molecular environment which promote changes in spin orientation while excess magnetic energy is coupled into other degrees of freedom by non-radiative processes. This is well known as spin-lattice relaxation. Certain dynamical processes cause fluctuations in the spin state energy levels leading to spin-spin relaxation and, here again, the environment at the molecular level plays a significant role in the magnitude of interaction. Relatively few electron spin relaxation studies of solutions have been conducted and the present work is addressed toward the extension of our knowledge in this area and the retrieval of dynamical information from line shape analyses on a time scale comparable to diffusion controlled phenomena.

Specifically, the electron spin relaxation of three Mn⁺²3d⁵ complexes, Mn(CH₃CN)₆⁺², MnCl₄^-2 in acetonitrile has been studied in considerable detail. The effective spin Hamiltonian constants were carefully evaluated under a wide range of experimental conditions. Resonance widths of these Mn⁺² complexes were studied in the presence of various excess ligand ions and as a function of concentration, viscosity, temperature and frequency (X-band, ~9.5 Ԍ Hz and K-band, ~35 Ԍ Hz).

A number of interesting conclusions were drawn from these studies. For the Et₄NCl-₄^-2 system several relaxation mechanisms leading to resonance broadening were observed. One source appears to arise through spin-orbit interactions caused by modulation of the ligand field resulting from transient distortions of the complex imparted by solvent fluctuations in the immediate surroundings of the paramagnetic ion. An additional spin relaxation was assigned to the formation of ion pairs [Et₄N⁺…MnCl₄^-2] and it was possible to estimate the dissociation constant for this specie in acetonitrile.

The Bu₄NBr-MnBr₄^-2 study was considerably more interesting. As in the former case, solvent fluctuations and ion-pairing of the paramagnetic complex [Bu₄N⁺…MnBr₄^-2] provide significant relaxation for the electronic spin system. Most interesting, without doubt, is the onset of a new relaxation mechanism leading to resonance broadening which is best interpreted as chemical exchange. Thus, assuming that resonance widths were simply governed by electron spin state lifetimes, we were able to extract dynamical information from an interaction in which the initial and final states are the same

MnBr₄^-2 + Br^- = MnBr₄^-2 + Br^-.

The bimolecular rate constants were obtained at six different temperatures and their magnitudes suggested that the exchange is probably diffusion controlled with essentially a zero energy of activation. The most important source of spin relaxation in this system stems directly from dipolar interactions between the manganese 3d⁵ electrons. Moreover, the dipolar broadening is strongly frequency dependent indicating a deviation between the transverse and longitudinal relaxation times. We are led to the conclusion that the 3d⁵ spin states of ion-paired MnBr₄^-2 are significantly correlated so that dynamical processes are also entering the picture. It was possible to estimate the correlation time, ^Td, characterizing this dynamical process.

In Part II we study nuclear magnetic relaxation of bromine ions in the MnBr4-2-Bu4NBr-acetonitrile system. Essentially we monitor the 79Br and 81Br linewidths in response to the [MnBr4-2]/[Br-] ratio with the express purpose of supporting our contention that exchange is occurring between "free" bromine ions in the solvent and bromine in the first coordination sphere of the paramagnetic anion. The complexity of the system elicited a two-part study: (1) the linewidth behavior of Bu4NBr in anhydrous CH3CN in the absence of MnBr4-2 and (2) in the presence of MnBr4-2. It was concluded in study (1) that dynamical association, Bu4NBr k1= Bu4N+ + Br-, was modulating field-gradient interactions at frequencies high enough to provide an estimation of the unimolecular rate constant, k1. A comparison of the two isotopic bromine linewidth-mole fraction results led to the conclusion that quadrupole interactions provided the dominant relaxation mechanism. In study (2) the "residual" bromine linewidths for both 79Br and 81Br are clearly controlled by quadrupole interactions which appear to be modulated by very rapid dynamical processes other than molecular reorientation. We conclude that the "residual" linewidth has its origin in chemical exchange and that bromine nuclei exchange rapidly between a "free" solvated ion and the paramagnetic complex, MnBr4-2.