The high flow rate that results as fluid decompresses through the restrictor is arguably the single greatest problem with supercritical fluid extraction techniques. As a result of these high flow rates, solvent trapping is not efficient in many cases, and the more complicated sorbent trapping technique must be used. In addition, loss of the collection solvent may occur during the process making it difficult to work with small volumes, which are desirable from the standpoint of sensitivity, cost, and environmental concerns. Similarly, these high decompressed flows have made it difficult to directly interface supercritical fluid extraction methods with separation techniques. This is unfortunate as supercritical extractions are ideal for on-line coupling in other respects, such as the fact that the fluid becomes gaseous upon depressurization and that supercritical fluids generally extract less contaminant material. In this thesis we have shown that, by elevating the post-restrictor pressure, the decompressed flow rate can be reduced, and these problems can be minimized, considerably. Off-line trapping becomes much simpler when working at elevated pressures as the need for sorbent trapping is virtually eliminated and solvent trapping may be conducted with much less difficulty. Elevated post-restrictor pressures were found to be very beneficial for on-line work as well. SFE/GC was carried out with complete transfer of the extraction effluent to a capillary GC column, which has not previously been demonstrated. Likewise the use of an open-tubular column interface, maintained at moderately elevated pressures, allowed SFE/HPLC to be conducted with quantitative analyte transfer, even in the presence of 10% modifier. In all cases - but especially for the on-line methods - more practical extraction parameters were possible, including extraction vessel volume, extraction flow rate, and dynamic extraction time. Another benefit of elevating the post-restrictor pressure is that higher extraction flow rates will generally be possible. The benefits of this were not evaluated in the research presented here, however, the effect that the extraction flow rate can have on extraction time is considered, from a theoretical standpoint, in Chapter five. / Ph. D.

Historically, ocelots (Leopardus pardalis) were hunted in large numbers for their fur, causing declines in population abundance across their range. In recent decades protection measures (e.g. CITES) and decreased public demand for ocelot fur resulted in declines in hunting pressure. Do to their elusive nature there is little known about ocelot population size, structure or general ecology. This lack of information hampers our ability to provide protection for this endangered species. Remote cameras were deployed in 7 grids across the landscape to estimate the density of ocelots in 2 habitat types; the broadleaf rainforest and pine forest of western Belize. Camera trapping combined with mark-recapture statistics resulted in densities of 18.91 - 20.75 ocelots per 100 km2 in the rainforest and 2.31 0 3.81 ocelots per 100 km2 in the pine forest habitat. This study examined the issues of camera spacing and animals with zero distance moved and their effect on density estimation. Increased camera spacing resulted in larger buffer sizes (increasing the effective trap area) and decreased density estimates. Inclusion of zero distance animals decreased buffer sizes and increased density estimates. Regardless of these effects, ocelot density was higher in the broadleaf rainforest than the pine forest. The ocelot density estimates in Belizean forests were lower than those in other portions of their range. The camera trapping technique demonstrated ocelots to be mostly active at night, with peaks of activity after sunset and before sunrise, and to travel low-use roads in the wet season and high-use roads in the dry season. Radio telemetry was used in this study to estimate the home range size and density of ocelots in the broadleaf rainforest of western Belize. Six collared ocelots (3 male, 3 female) were collared and tracked from September 2003 - August 2004. Male ocelots had an average home range size of 33.01 km2 (95% fixed kernel) and 29.00 km2 (100% MCP), and female ocelots had an average home range size of 21.05 km2 (95% fixed kernel) and 29.58 km2 (100% MCP). Most ocelots had larger home ranges in the dry season than the wet season. Ocelots showed a large amount of same sex home range overlap; with male-male overlap averaging 25% (100% MCP) and female-female overlap averaging 16% (100% MCP). Ocelot density determined using radio telemetry was 7.79 - 10.91 ocelots per 100 km2. The radio telemetry ocelot densities were lower and their home ranges larger in the Belizean broadleaf rainforests than those in other portions of their range. The camera trapping and radio telemetry techniques were compared against one another and combined in order to test which technique may be more successful in studying certain aspects of feline behavior. Activity budgets and density estimates determined from camera trapping were superior to radio telemetry, whereas camera trapping home ranges showed higher variation and lower resolution than radio telemetry. However, home range estimates determined from camera trapping captured long distance movements, a larger percent of territory overlap, and displayed potential for estimating an animal's core use area. When radio telemetry data were used to create a buffer around camera traps based on the average radius of an ocelots' home range size, the resulting density estimates were smaller than those determined using the current camera trapping methodology. This study provided much needed baseline information on ocelot abundance, home range size, activity patterns, and trail use. While sample sizes were small, this study had the largest number of ocelots captured in Central America to date. Although camera trapping is already a useful tool in felid research, this study highlights the importance of further standardization of the camera trapping methodology, increasing its potential for monitoring and conservation across habitats and study sites. / Master of Science

Electrochromic thin films can effectively regulate the visible and infrared light passing through a window, demonstrating great potential to save energy and offer a comfortable indoor environment in buildings. However, long-term durability is a big issue and the physics behind this is far from clear. This dissertation work concerns two important parts of an electrochromic window: the anodic and cathodic layers. In particular, work focusing on the anodic side develop a new Ni oxide based layers and uncover degradation dynamics in Ni oxide thin films; and work focusing on the cathodic side addresses materials rejuvenation with the aim to eliminate degradation. In the first part of this dissertation work, iridium oxide is found to be compatible with acids, bases and Li+-containing electrolytes, and an anodic layer with very superior long-term durability was developed by incorporating of small amount (7.6 at. %) of Ir into Ni oxide. This film demonstrated sustained cycle-dependent growth of charge density and electrochromic modulation even after 10,000 CV cycles. The (111) and (100) crystal facets in Ni oxide are found to possess different abilities to absorb cation and/or anion, which yields different degrees of coloration and this is very significant for the electrochromic properties. The degradation of charge capacity in Ni oxide has an inevitable rapid decay in the first hundreds of cycles, subsequently combined with a more gradual decay, which is independent of applied potential and film composition. The consistent phenomenon can be very well modeled by power-law or stretched exponential decay; however the two models are indistinguishable in the current stage. Interestingly, in both models, the power-law exponent is 0.2 ≤ p ≤ 0.8, with most of the values around 0.5, in line with normal or anomalous diffusion models. The second part of dissertation work deals with cathodic WO3 and TiO2. WO3 suffers from ion trapping induced degradation of charge capacity and optical modulation upon electrochemical cycling. This speculation is strongly supported by direct evidence from Time-of-Flight Elastic Recoil Detection Analysis (ToF-ERDA). Most importantly, this ion trapping induced degradation can be eliminated by a galvanostatic de-trapping process. Significant ion-trapping takes place when x exceeds ~0.65 in LixWO3. The trapped ions are stable in the host structure, meaning that the ions cannot de-trap without external stimuli. The similar work done on TiO2 significantly complements and extends the work on the recuperation of WO3; the difference is that the trapped ions in host TiO2 seem to be less stable compared with the trapped ions in WO3.     Overall, this dissertation presents a refined conceptual framework for developing superior electrochromic windows in energy efficient buildings.

Les codes Low-Density Parity-Check (LDPC) sont au coeur de larecherche des codes correcteurs d'erreurs en raison de leur excellenteperformance de décodage en utilisant un algorithme de décodageitératif de type propagation de croyances (Belief Propagation - BP).Cet algorithme utilise la représentation graphique d'un code, ditgraphe de Tanner, et calcule les fonctions marginales sur le graphe.Même si l'inférence calculée n'est exacte que sur un graphe acyclique(arbre), l'algorithme BP estime de manière très proche les marginalessur les graphes cycliques, et les codes LDPC peuvent asymptotiquementapprocher la capacité de Shannon avec cet algorithme.Cependant, sur des codes de longueurs finies dont la représentationgraphique contient des cycles, l'algorithme BP est sous-optimal etdonne lieu à l'apparition du phénomène dit de plancher d'erreur. Leplancher d'erreur se manifeste par la dégradation soudaine de la pentedu taux d'erreur dans la zone de fort rapport signal à bruit où lesstructures néfastes au décodage sont connues en termes de TrappingSets présents dans le graphe de Tanner du code, entraînant un échec dudécodage. De plus, les effets de la quantification introduite parl'implémentation en hardware de l'algorithme BP peuvent amplifier ceproblème de plancher d'erreur.Dans cette thèse nous introduisons un nouveau paradigme pour ledécodage itératif à précision finie des codes LDPC sur le canalbinaire symétrique. Ces nouveaux décodeurs, appelés décodeursitératifs à alphabet fini (Finite Alphabet Iterative Decoders – FAID)pour préciser que les messages appartiennent à un alphabet fini, sontcapables de surpasser l'algorithme BP dans la région du plancherd'erreur. Les messages échangés par les FAID ne sont pas desprobabilités ou vraisemblances quantifiées, et les fonctions de miseà jour des noeuds de variable ne copient en rien le décodage par BP cequi contraste avec les décodeurs BP quantifiés traditionnels. Eneffet, les fonctions de mise à jour sont de simples tables de véritéconçues pour assurer une plus grande capacité de correction d'erreuren utilisant la connaissance de topologies potentiellement néfastes audécodage présentes dans un code donné. Nous montrons que sur demultiples codes ayant un poids colonne de trois, il existe des FAIDutilisant 3 bits de précision pouvant surpasser l'algorithme BP(implémenté en précision flottante) dans la zone de plancher d'erreursans aucun compromis dans la latence de décodage. C'est pourquoi lesFAID obtiennent des performances supérieures comparées au BP avecseulement une fraction de sa complexité.Par ailleurs, nous proposons dans cette thèse une décimation amélioréedes FAID pour les codes LDPC dans le traitement de la mise à jour desnoeuds de variable. La décimation implique de fixer certains bits ducode à une valeur particulière pendant le décodage et peut réduire demanière significative le nombre d'itérations requises pour corriger uncertain nombre d'erreurs fixé tout en maintenant de bonnesperformances d'un FAID, le rendant plus à même d'être analysé. Nousillustrons cette technique pour des FAID utilisant 3 bits de précisioncodes de poids colonne trois. Nous montrons également comment cettedécimation peut être utilisée de manière adaptative pour améliorer lescapacités de correction d'erreur des FAID. Le nouveau modèle proposéde décimation adaptative a, certes, une complexité un peu plus élevée,mais améliore significativement la pente du plancher d'erreur pour unFAID donné. Sur certains codes à haut rendement, nous montrons que ladécimation adaptative des FAID permet d'atteindre des capacités decorrection d'erreur proches de la limite théorique du décodage au sensdu maximum de vraisemblance. / At the heart of modern coding theory lies the fact that low-density parity-check (LDPC) codes can be efficiently decoded by message-passing algorithms which are traditionally based on the belief propagation (BP) algorithm. The BP algorithm operates on a graphical model of a code known as the Tanner graph, and computes marginals of functions on the graph. While inference using BP is exact only on loop-free graphs (trees), the BP still provides surprisingly close approximations to exact marginals on loopy graphs, and LDPC codes can asymptotically approach Shannon's capacity under BP decoding.However, on finite-length codes whose corresponding graphs are loopy, BP is sub-optimal and therefore gives rise to the error floor phenomenon. The error floor is an abrupt degradation in the slope of the error-rate performance of the code in the high signal-to-noise regime, where certain harmful structures generically termed as trapping sets present in the Tanner graph of the code, cause the decoder to fail. Moreover, the effects of finite precision that are introduced during hardware realizations of BP can further contribute to the error floor problem.In this dissertation, we introduce a new paradigm for finite precision iterative decoding of LDPC codes over the Binary Symmetric channel (BSC). These novel decoders, referred to as finite alphabet iterative decoders (FAIDs) to signify that the message values belong to a finite alphabet, are capable of surpassing the BP in the error floor region. The messages propagated by FAIDs are not quantized probabilities or log-likelihoods, and the variable node update functions do not mimic the BP decoder, which is in contrast to traditional quantized BP decoders. Rather, the update functions are simple maps designed to ensure a higher guaranteed error correction capability by using the knowledge of potentially harmful topologies that could be present in a given code. We show that on several column-weight-three codes of practical interest, there exist 3-bit precision FAIDs that can surpass the BP (floating-point) in the error floor without any compromise in decoding latency. Hence, they are able to achieve a superior performance compared to BP with only a fraction of its complexity.Additionally in this dissertation, we propose decimation-enhanced FAIDs for LDPC codes, where the technique of decimation is incorporated into the variable node update function of FAIDs. Decimation, which involves fixing certain bits of the code to a particular value during the decoding process, can significantly reduce the number of iterations required to correct a fixed number of errors while maintaining the good performance of a FAID, thereby making such decoders more amenable to analysis. We illustrate this for 3-bit precision FAIDs on column-weight-three codes. We also show how decimation can be used adaptively to further enhance the guaranteed error correction capability of FAIDs that are already good on a given code. The new adaptive decimation scheme proposed has marginally added complexity but can significantly improve the slope of the error floor performance of a particular FAID. On certain high-rate column-weight-three codes of practical interest, we show that adaptive decimation-enhanced FAIDs can achieve a guaranteed error-correction capability that is close to the theoretical limit achieved by maximum-likelihood decoding.

A study of the aquatic invertebrate communities from two locations (Location 1 and Location 2) within the Matapouri catchment in Northland, New Zealand, was conducted to assess community structure in differing local-scale habitats. Four data collection methods were utilised generating 33,058 adult or larval invertebrates. The sampling methods comprised benthic kick-sampling, sticky trapping, light trapping, and emergence trapping. For the sticky trapping and light trapping, sampling was carried out at three different sites (Sites 1–3) within each location. The sites were situated within three habitat types; native forest, native forest-fringe, and raupo wetland. Emergence trapping also commenced within the three sites, at both locations, but was discontinued after two months, due to the equipment being destroyed by consecutive flooding events (method described in Appendix 1). Benthic sampling was carried out within the Forest and Forest-fringe habitats. Benthic sampling, sticky trapping, and light trapping were carried out following a monthly schedule between June and November 2005. Conductivity, pH, and water temperature measurements were taken concurrently with benthic sampling on a monthly basis, while water velocity and substrate measurements were taken once to assist in habitat characterisation. Overall, 71 taxa were recorded by benthic sampling over the six month period, with a mean of approximately 30 taxa per site per month. In comparison with similar studies elsewhere in New Zealand, a figure of around 30 taxa per sample was high. The benthic macroinvertebrate fauna at all sites was dominated by Trichoptera (19 taxa), Diptera (16 taxa) and Ephemeroptera (10 taxa). This pattern of diversity is similar to that reported in other New Zealand studies. However, in contrast to previous studies, the leptophlebiid mayfly genus Deleatidium was not numerically dominant over the rest of the community, and other leptophlebiid genera (Acanthophlebia, Atalophlebioides, Mauiulus and Zephlebia) were equally represented, possibly reflecting niche partitioning between the groups. The genus Nesameletus was not recorded at any site, despite being one of the core mayfly species in New Zealand streams. The rare mayfly Isothraulus abditus was recorded at one of the forest locations. There are no published records of this species from Northland. Although acknowledged as another of the core New Zealand benthic taxa, the hydropsychid caddisfly Aoteapsyche was not recorded during the study. However, another hydropsychid, Orthopsyche, was commonly recorded, and these may be filling a similar niche to the Aoteapsyche genus. In contrast to the Trichoptera, Diptera, and Ephemeroptera, the Plecoptera fauna was relatively depauperate, probably reflecting the warmer climate of the region and lack of temperature-buffered spring-fed streams. Surprisingly, Zelandobius, a core New Zealand genus, was absent but is regularly recorded in Northland. A species of conservation interest, Spaniocercoides watti, currently recognised as a Northland endemic, was recorded in low numbers. There were no apparent trends in diversity or abundance of benthic invertebrates over time. Also, there were no significant differences in species diversity between the two locations. However, in many cases, taxa were more abundant at Location 2. This may have been due to steeper gradients at Location 2, and the consequent effects on substrate size and streambed stability, as all other physical factors appeared similar between locations. Although several significant differences of individual benthic taxa were recorded, no broad effect of habitat (sites) on species diversity was observable. However, at Location 2, abundances were significantly higher at Site 3 (Forest) compared to Site 2 (Forest-fringe). The reasons were uncertain, but may be attributed to higher retention of allochthonous organic materials, trapped by in-stream cover and larger substrates. Investigations of adult stages by sticky traps supported benthic results recording community compositions and abundances dominated by Trichoptera and Diptera. Plecoptera were poorly represented. Location 2 recorded higher abundances of taxa, particularly Ephemeroptera and Plecoptera. Investigations of adult stages by light traps however did not produce any statistically significant differences in abundances between sites, between locations, or between sites across locations, and it is believed to be due to limited sampling replication combined with some biases of light trapping. This study indicates that the aquatic invertebrate community at Matapouri is diverse but also reasonably representative. Several rare or uncommon insects inhabit the catchment. It is therefore important that Iwi and the local Landcare Group, who invited and supported this research, together with the Department of Conservation, continue their efforts in protecting these areas. The resident fauna have the capacity to restock areas downstream, which are intended to be improved and restored through sediment control and riparian management.

Thesis (Ph. D.)--University of Oregon, 2003. / Typescript. Includes vita and abstract. Includes bibliographical references (leaves 634-646). Also available for download via the World Wide Web; free to University of Oregon users.

In response to the recent delisting of the bald eagle as an endangered species, the Three Affiliated Tribes of the Fort Berthold Indian Reservation, the University of Arizona, and the National Park Service undertook this collaborative study to identify continuities and discontinuities in eagle knowledge and acquisition and use of eagle parts by members of the Mandan, Hidatsa, and Arikara Nation (MHA), and to document cultural resources associated with eagles in three North Dakota national parks. Interviews with tribal consultants who possess eagle rights were integrated with ethnographic, archaeological, and archival data. This research finds that although there have been major changes in how MHA people acquire eagles for personal and religious use since the early 20`" century, beliefs and practices associated with eagle demonstrate cultural continuity. There remains a strict adherence to protocols regarding the handling of eagles and the possession and transfer of eagle knowledge, and there is a persistent belief in the eagle's ability to animate people, objects, and places. The eagle feather remains an indicator of social status, spiritual power, and identity, and eagle parts continue to be crucial elements in the performance of major religious ceremonies. Several site types associated with eagles and eagle trapping were identified, and all three parks either contain eagle resources, or are associated with parts of the eagle landscape. While trapping pits and trapping lodges are no longer used for taking eagles, they retain significance as sources of supernatural power and spiritual knowledge. These sites are spiritually active, and are important places for conducting fasts, seeking visions, and making religious offerings. Tribal consultants believe that the power imbued in these sites is attributed to their past role in the establishment and perpetuation of relationships between their ancestors and the spiritual world during annual trapping expeditions. Both site types are culturally significant in their familial and clan associations, their reflection of traditional land uses unique to the Missouri River environs, and their role in the transformative religious experiences of ancestors. There is a desire within the tribal community to preserve eagle trapping pit sites and, even more so, trapping lodge sites. In order to maintain the sites' spiritual integrity, consultants prefer that they not be accessible to the general public.

A study of the aquatic invertebrate communities from two locations (Location 1 and Location 2) within the Matapouri catchment in Northland, New Zealand, was conducted to assess community structure in differing local-scale habitats. Four data collection methods were utilised generating 33,058 adult or larval invertebrates. The sampling methods comprised benthic kick-sampling, sticky trapping, light trapping, and emergence trapping. For the sticky trapping and light trapping, sampling was carried out at three different sites (Sites 1–3) within each location. The sites were situated within three habitat types; native forest, native forest-fringe, and raupo wetland. Emergence trapping also commenced within the three sites, at both locations, but was discontinued after two months, due to the equipment being destroyed by consecutive flooding events (method described in Appendix 1). Benthic sampling was carried out within the Forest and Forest-fringe habitats. Benthic sampling, sticky trapping, and light trapping were carried out following a monthly schedule between June and November 2005. Conductivity, pH, and water temperature measurements were taken concurrently with benthic sampling on a monthly basis, while water velocity and substrate measurements were taken once to assist in habitat characterisation. Overall, 71 taxa were recorded by benthic sampling over the six month period, with a mean of approximately 30 taxa per site per month. In comparison with similar studies elsewhere in New Zealand, a figure of around 30 taxa per sample was high. The benthic macroinvertebrate fauna at all sites was dominated by Trichoptera (19 taxa), Diptera (16 taxa) and Ephemeroptera (10 taxa). This pattern of diversity is similar to that reported in other New Zealand studies. However, in contrast to previous studies, the leptophlebiid mayfly genus Deleatidium was not numerically dominant over the rest of the community, and other leptophlebiid genera (Acanthophlebia, Atalophlebioides, Mauiulus and Zephlebia) were equally represented, possibly reflecting niche partitioning between the groups. The genus Nesameletus was not recorded at any site, despite being one of the core mayfly species in New Zealand streams. The rare mayfly Isothraulus abditus was recorded at one of the forest locations. There are no published records of this species from Northland. Although acknowledged as another of the core New Zealand benthic taxa, the hydropsychid caddisfly Aoteapsyche was not recorded during the study. However, another hydropsychid, Orthopsyche, was commonly recorded, and these may be filling a similar niche to the Aoteapsyche genus. In contrast to the Trichoptera, Diptera, and Ephemeroptera, the Plecoptera fauna was relatively depauperate, probably reflecting the warmer climate of the region and lack of temperature-buffered spring-fed streams. Surprisingly, Zelandobius, a core New Zealand genus, was absent but is regularly recorded in Northland. A species of conservation interest, Spaniocercoides watti, currently recognised as a Northland endemic, was recorded in low numbers. There were no apparent trends in diversity or abundance of benthic invertebrates over time. Also, there were no significant differences in species diversity between the two locations. However, in many cases, taxa were more abundant at Location 2. This may have been due to steeper gradients at Location 2, and the consequent effects on substrate size and streambed stability, as all other physical factors appeared similar between locations. Although several significant differences of individual benthic taxa were recorded, no broad effect of habitat (sites) on species diversity was observable. However, at Location 2, abundances were significantly higher at Site 3 (Forest) compared to Site 2 (Forest-fringe). The reasons were uncertain, but may be attributed to higher retention of allochthonous organic materials, trapped by in-stream cover and larger substrates. Investigations of adult stages by sticky traps supported benthic results recording community compositions and abundances dominated by Trichoptera and Diptera. Plecoptera were poorly represented. Location 2 recorded higher abundances of taxa, particularly Ephemeroptera and Plecoptera. Investigations of adult stages by light traps however did not produce any statistically significant differences in abundances between sites, between locations, or between sites across locations, and it is believed to be due to limited sampling replication combined with some biases of light trapping. This study indicates that the aquatic invertebrate community at Matapouri is diverse but also reasonably representative. Several rare or uncommon insects inhabit the catchment. It is therefore important that Iwi and the local Landcare Group, who invited and supported this research, together with the Department of Conservation, continue their efforts in protecting these areas. The resident fauna have the capacity to restock areas downstream, which are intended to be improved and restored through sediment control and riparian management.

A study of the aquatic invertebrate communities from two locations (Location 1 and Location 2) within the Matapouri catchment in Northland, New Zealand, was conducted to assess community structure in differing local-scale habitats. Four data collection methods were utilised generating 33,058 adult or larval invertebrates. The sampling methods comprised benthic kick-sampling, sticky trapping, light trapping, and emergence trapping. For the sticky trapping and light trapping, sampling was carried out at three different sites (Sites 1–3) within each location. The sites were situated within three habitat types; native forest, native forest-fringe, and raupo wetland. Emergence trapping also commenced within the three sites, at both locations, but was discontinued after two months, due to the equipment being destroyed by consecutive flooding events (method described in Appendix 1). Benthic sampling was carried out within the Forest and Forest-fringe habitats. Benthic sampling, sticky trapping, and light trapping were carried out following a monthly schedule between June and November 2005. Conductivity, pH, and water temperature measurements were taken concurrently with benthic sampling on a monthly basis, while water velocity and substrate measurements were taken once to assist in habitat characterisation. Overall, 71 taxa were recorded by benthic sampling over the six month period, with a mean of approximately 30 taxa per site per month. In comparison with similar studies elsewhere in New Zealand, a figure of around 30 taxa per sample was high. The benthic macroinvertebrate fauna at all sites was dominated by Trichoptera (19 taxa), Diptera (16 taxa) and Ephemeroptera (10 taxa). This pattern of diversity is similar to that reported in other New Zealand studies. However, in contrast to previous studies, the leptophlebiid mayfly genus Deleatidium was not numerically dominant over the rest of the community, and other leptophlebiid genera (Acanthophlebia, Atalophlebioides, Mauiulus and Zephlebia) were equally represented, possibly reflecting niche partitioning between the groups. The genus Nesameletus was not recorded at any site, despite being one of the core mayfly species in New Zealand streams. The rare mayfly Isothraulus abditus was recorded at one of the forest locations. There are no published records of this species from Northland. Although acknowledged as another of the core New Zealand benthic taxa, the hydropsychid caddisfly Aoteapsyche was not recorded during the study. However, another hydropsychid, Orthopsyche, was commonly recorded, and these may be filling a similar niche to the Aoteapsyche genus. In contrast to the Trichoptera, Diptera, and Ephemeroptera, the Plecoptera fauna was relatively depauperate, probably reflecting the warmer climate of the region and lack of temperature-buffered spring-fed streams. Surprisingly, Zelandobius, a core New Zealand genus, was absent but is regularly recorded in Northland. A species of conservation interest, Spaniocercoides watti, currently recognised as a Northland endemic, was recorded in low numbers. There were no apparent trends in diversity or abundance of benthic invertebrates over time. Also, there were no significant differences in species diversity between the two locations. However, in many cases, taxa were more abundant at Location 2. This may have been due to steeper gradients at Location 2, and the consequent effects on substrate size and streambed stability, as all other physical factors appeared similar between locations. Although several significant differences of individual benthic taxa were recorded, no broad effect of habitat (sites) on species diversity was observable. However, at Location 2, abundances were significantly higher at Site 3 (Forest) compared to Site 2 (Forest-fringe). The reasons were uncertain, but may be attributed to higher retention of allochthonous organic materials, trapped by in-stream cover and larger substrates. Investigations of adult stages by sticky traps supported benthic results recording community compositions and abundances dominated by Trichoptera and Diptera. Plecoptera were poorly represented. Location 2 recorded higher abundances of taxa, particularly Ephemeroptera and Plecoptera. Investigations of adult stages by light traps however did not produce any statistically significant differences in abundances between sites, between locations, or between sites across locations, and it is believed to be due to limited sampling replication combined with some biases of light trapping. This study indicates that the aquatic invertebrate community at Matapouri is diverse but also reasonably representative. Several rare or uncommon insects inhabit the catchment. It is therefore important that Iwi and the local Landcare Group, who invited and supported this research, together with the Department of Conservation, continue their efforts in protecting these areas. The resident fauna have the capacity to restock areas downstream, which are intended to be improved and restored through sediment control and riparian management.

<p>To achieving successfully commercial nuclear fusion energy, fully understanding of the interaction between plasma particles and plasma facing components is one of the essential issues. Tungsten, due to good thermal and mechanical properties such as high thermal conductivity and melting temperature, is one of the most promising candidates. However, the plasma facing components interacting with the extreme environmental conditions such as high temperature and radiation may lead to nanostructure formation, sputtering and erosion that will lead to material degradation. And these deformations may influence not only properties of plasma facing components but also might affect the plasma itself. For example, the contamination of plasma with a few amounts of tungsten, a high Z element, as a result of erosion or sputtering may cause core plasma cooling that results in loss of plasma confinement. Additionally, the retention of hydrogen isotopes, especially tritium, in tungsten is essential issue because of its radioactivity and market value.</p> In this study, deuterium trapping in tungsten is analyzed by molecular dynamics method and the effect of pre-irradiation on trapping is studied. Non-cumulative studies show that the increase in the energy of hydrogen isotopes rises the absorption rate, the initial implantation depth, and the average resting time for initial implantation. Additionally, the effect of implanted deuterium due to pre-irradiation on the hydrogen isotopes trapping is analyzed by combining both cumulative and non-cumulative simulations, and results indicate that while the increase in the pre-irradiation time raises the absorption rate of deuterium with higher energy than 80 eV, it causes a decrease the initial implantation depth and the average resting time for initial implantation because of deuterium-deuterium interactions. Additionally, the deuterium-deuterium interactions may transfer enough energy to implanted deuterium to start a motion which may lead to deeper implantation or escaping from the surface of tungsten. The escaping from surface as a result of deuterium-deuterium interaction could explain the decrease in accumulation rate of deuterium while absorption rate rises.