5,795 research outputs found
Design and Evaluation of a Hardware System for Online Signal Processing within Mobile Brain-Computer Interfaces
Brain-Computer Interfaces (BCIs) sind innovative Systeme, die eine direkte Kommunikation zwischen dem Gehirn und externen GerĂ€ten ermöglichen. Diese Schnittstellen haben sich zu einer transformativen Lösung nicht nur fĂŒr Menschen mit neurologischen Verletzungen entwickelt, sondern auch fĂŒr ein breiteres Spektrum von Menschen, das sowohl medizinische als auch nicht-medizinische Anwendungen umfasst. In der Vergangenheit hat die Herausforderung, dass neurologische Verletzungen nach einer anfĂ€nglichen Erholungsphase statisch bleiben, die Forscher dazu veranlasst, innovative Wege zu beschreiten. Seit den 1970er Jahren stehen BCIs an vorderster Front dieser BemĂŒhungen. Mit den Fortschritten in der Forschung haben sich die BCI-Anwendungen erweitert und zeigen ein groĂes Potenzial fĂŒr eine Vielzahl von Anwendungen, auch fĂŒr weniger stark eingeschrĂ€nkte (zum Beispiel im Kontext von Hörelektronik) sowie völlig gesunde Menschen (zum Beispiel in der Unterhaltungsindustrie). Die Zukunft der BCI-Forschung hĂ€ngt jedoch auch von der VerfĂŒgbarkeit zuverlĂ€ssiger BCI-Hardware ab, die den Einsatz in der realen Welt gewĂ€hrleistet.
Das im Rahmen dieser Arbeit konzipierte und implementierte CereBridge-System stellt einen bedeutenden Fortschritt in der Brain-Computer-Interface-Technologie dar, da es die gesamte Hardware zur Erfassung und Verarbeitung von EEG-Signalen in ein mobiles System integriert. Die Architektur der Verarbeitungshardware basiert auf einem FPGA mit einem ARM Cortex-M3 innerhalb eines heterogenen ICs, was FlexibilitĂ€t und Effizienz bei der EEG-Signalverarbeitung gewĂ€hrleistet. Der modulare Aufbau des Systems, bestehend aus drei einzelnen Boards, gewĂ€hrleistet die Anpassbarkeit an unterschiedliche Anforderungen. Das komplette System wird an der Kopfhaut befestigt, kann autonom arbeiten, benötigt keine externe Interaktion und wiegt einschlieĂlich der 16-Kanal-EEG-Sensoren nur ca. 56 g. Der Fokus liegt auf voller MobilitĂ€t.
Das vorgeschlagene anpassbare Datenflusskonzept erleichtert die Untersuchung und nahtlose Integration von Algorithmen und erhöht die FlexibilitĂ€t des Systems. Dies wird auch durch die Möglichkeit unterstrichen, verschiedene Algorithmen auf EEG-Daten anzuwenden, um unterschiedliche Anwendungsziele zu erreichen. High-Level Synthesis (HLS) wurde verwendet, um die Algorithmen auf das FPGA zu portieren, was den Algorithmenentwicklungsprozess beschleunigt und eine schnelle Implementierung von Algorithmusvarianten ermöglicht. Evaluierungen haben gezeigt, dass das CereBridge-System in der Lage ist, die gesamte Signalverarbeitungskette zu integrieren, die fĂŒr verschiedene BCI-Anwendungen erforderlich ist. DarĂŒber hinaus kann es mit einer Batterie von mehr als 31 Stunden Dauerbetrieb betrieben werden, was es zu einer praktikablen Lösung fĂŒr mobile Langzeit-EEG-Aufzeichnungen und reale BCI-Studien macht.
Im Vergleich zu bestehenden Forschungsplattformen bietet das CereBridge-System eine bisher unerreichte LeistungsfĂ€higkeit und Ausstattung fĂŒr ein mobiles BCI. Es erfĂŒllt nicht nur die relevanten Anforderungen an ein mobiles BCI-System, sondern ebnet auch den Weg fĂŒr eine schnelle Ăbertragung von Algorithmen aus dem Labor in reale Anwendungen. Im Wesentlichen liefert diese Arbeit einen umfassenden Entwurf fĂŒr die Entwicklung und Implementierung eines hochmodernen mobilen EEG-basierten BCI-Systems und setzt damit einen neuen Standard fĂŒr BCI-Hardware, die in der Praxis eingesetzt werden kann.Brain-Computer Interfaces (BCIs) are innovative systems that enable direct communication between the brain and external devices. These interfaces have emerged as a transformative solution not only for individuals with neurological injuries, but also for a broader range of individuals, encompassing both medical and non-medical applications. Historically, the challenge of neurological injury being static after an initial recovery phase has driven researchers to explore innovative avenues. Since the 1970s, BCIs have been at one forefront of these efforts. As research has progressed, BCI applications have expanded, showing potential in a wide range of applications, including those for less severely disabled (e.g. in the context of hearing aids) and completely healthy individuals (e.g. entertainment industry). However, the future of BCI research also depends on the availability of reliable BCI hardware to ensure real-world application.
The CereBridge system designed and implemented in this work represents a significant leap forward in brain-computer interface technology by integrating all EEG signal acquisition and processing hardware into a mobile system. The processing hardware architecture is centered around an FPGA with an ARM Cortex-M3 within a heterogeneous IC, ensuring flexibility and efficiency in EEG signal processing. The modular design of the system, consisting of three individual boards, ensures adaptability to different requirements. With a focus on full mobility, the complete system is mounted on the scalp, can operate autonomously, requires no external interaction, and weighs approximately 56g, including 16 channel EEG sensors.
The proposed customizable dataflow concept facilitates the exploration and seamless integration of algorithms, increasing the flexibility of the system. This is further underscored by the ability to apply different algorithms to recorded EEG data to meet different application goals. High-Level Synthesis (HLS) was used to port algorithms to the FPGA, accelerating the algorithm development process and facilitating rapid implementation of algorithm variants. Evaluations have shown that the CereBridge system is capable of integrating the complete signal processing chain required for various BCI applications. Furthermore, it can operate continuously for more than 31 hours with a 1800mAh battery, making it a viable solution for long-term mobile EEG recording and real-world BCI studies.
Compared to existing research platforms, the CereBridge system offers unprecedented performance and features for a mobile BCI. It not only meets the relevant requirements for a mobile BCI system, but also paves the way for the rapid transition of algorithms from the laboratory to real-world applications. In essence, this work provides a comprehensive blueprint for the development and implementation of a state-of-the-art mobile EEG-based BCI system, setting a new benchmark in BCI hardware for real-world applicability
Ruthenium metallotherapeutics: a targeted approach to combatting multidrug resistant pathogens
The discovery of antibiotics revolutionised healthcare practice. However due to overuse, inappropriate use, widespread prophylaxis therapy and the lack of new developments, the threat of antimicrobial resistance is now a major global threat to health. By 2050, it is estimated that mortality due to antimicrobial resistant infections will exceed 10 million people per annum, superseding cancer as the leading cause of global mortality. The use of drug repurposing to identify potential therapies which combat antimicrobial resistance is one potential solution. Metals have been used as antimicrobial agents throughout the history of medicine for a broad range of applications, including the use of Silver as an antimicrobial agent which dates back to antiquity. More recently, Ruthenium metallotherapeutic complexes have been shown to exhibit highly active antimicrobial properties by targeting a range of bacterial species, and in contrast to traditional antibiotics, these compounds are thought to elicit antibacterial activity at multiple sites within the bacterial cell, which may reduce the possibility of resistance evolution. This study aimed to evaluate the antimicrobial activity of a series of Ruthenium metallotherapeutic complexes against multidrug-resistant bacterial pathogens, with a focus on use within wound care applications.
Antimicrobial susceptibility assays identified two lead candidates, Hexaammineruthenium (III) chloride and [Chlorido(η6-p-cymene)(N-(4-chlorophenyl)pyridine-2-carbothioamide) ruthenium (II)] chloride which demonstrated activity against Pseudomonas aeruginosa and Staphylococcus aureus respectively with MIC values ranging between 4 Όg mL-1 and 16 Όg mL-1. Furthermore, Hexaammineruthenium (III) chloride demonstrated antibiofilm activity in both a time and concentration-dependent manner. Synergy studies combining lead complexes with antibiotics demonstrated the potential for use as resistance breakers. Subsequent in vitro infection modelling using scratch assays with skin cell lines, coupled with a 3D full thickness skin wound infection model was used to determine potential applied applications of Hexaammineruthenium (III) chloride for use as topical antimicrobial agent against P. aeruginosa infections.
Antimicrobial mechanistic studies demonstrated that Hexaammineruthenium (III) chloride targeted the bacterial cell ultrastructure of P. aeruginosa strain PAO1 as cell perturbations were observed when treated cells were analysed by scanning electron microscopy. Furthermore, exposure of P. aeruginosa PAO1 to Hexaammineruthenium (III) chloride also resulted in a concentration dependent membrane depolarisation, which further supported the antimicrobial mechanistic role.
Finally, global changes in gene expression following exposure of P. aeruginosa strain PAO1 to Hexaammineruthenium (III) chloride were explored by RNA sequencing. Genes involved in ribosome function, cofactor biosynthesis and membrane fusion were downregulated, which provided a further insight into the wider mechanisms of antibacterial activity.
The research conducted in the present study indicated the potential use of Hexaammineruthenium (III) chloride (and derivatives) as a potential treatment option for chronic wounds infected with P. aeruginosa, which could be applied as either a direct treatment or used within antimicrobial wound care applications
The telecoupled sustainability impacts of global agricultural value chains:Assessing the cross-scale sustainability impacts of the cocoa sector
Agriculture is a major contributor to the global environmental crisis. Natural ecosystems are being replaced by agricultural land, which leads to the extinction of species and the release of tons of carbon emissions. Global agricultural value chains (GVCs) have grown due to the intensification of international trade. While GVCs have undeniably created economic opportunities for the agriculture sector, they have also led to the escalation of local environmental issues. Several initiatives have been implemented to reduce the negative impacts of agriculture, including government regulations, sustainability certification labels, and voluntary sustainability commitments. However, the effectiveness of these initiatives has been questioned due to several reasons, including the mismatches between the scale of the problem and the solution, the lack of monitoring and verification of sustainability actions, and their weak enforcement. Sustainability initiatives are informed by studies assessing the impacts of agriculture that often only focus on local impacts, while disregarding larger-scale â telecoupledâ dynamics that can trigger impacts across geographic and temporal scales. This thesis aims to help bridge these knowledge gaps by examining the impacts of agricultural GVCs across scales, studying the role of GVCâs configuration in modulating these impacts and investigating the role of GVC actors in mitigating sustainability risks across scales. The global cocoa value chain is used as a case study. Chapter 2 examines various impact assessment methods and their ability to capture the effects caused by telecoupled dynamics across different scales. The study concludes that no single method is sufficient to capture all telecoupled cross-scale dynamics and that the integration of different methods is necessary to bridge gaps between methods and complement their scope. Chapter 3 implements the recommendations outlined in Chapter 2 by analyzing the impacts caused by cocoa agroforestry and cocoa full-sun production in Ghana. Impacts on carbon, biodiversity stocks, and environmental pollution were analyzed within and beyond the farm-level. This chapter reveals that findings drawn from farm-level assessments can contradict those from landscape-level assessments. Decision-makers focused should be wary of extrapolating farm-level assessment results to larger scales. Chapter 4 expands the scope to the global scale by examining the role of the cocoa GVC configuration on the capacity of the sector to address sustainability challenges across scales. The chapter identifies different types of cocoa traders, their market dominance, and sustainability commitments. The chapter highlights that to address the telecoupled impacts of the cocoa GVC, coordinated action between traders is required, along with government interventions to balance power asymmetries. Chapter 5 measured the degree to which cocoa traders, as identified in Chapter 4, are exposed to deforestation and climate change. This chapter highlights that sustainability challenges in agricultural value chains cannot be resolved in isolation as farming systems are constantly interacting with other farming systems and land competing sectors. To avoid displacing negative impacts across scales, it is necessary to have a coordinated and collaborative effort from stakeholders and sectors involved in making decisions related to land use. This thesis shows that addressing the telecoupled impacts caused by agricultural value chains needs a good understanding of the cause-effect dynamics at play. This requires the quantification of impacts caused by agriculture across scales and the characterization of the GVC network of actors modulating these impacts. Interdisciplinary methods need to be leveraged and integrated to generate actionable insights. The findings of this thesis can assist decision-makers and private actors in devising customized sustainability strategies, prioritizing action, and addressing the most vulnerable hotspots while being mindful of global teleconnections and avoiding spillovers
Machine Learning Approach to Investigating the Relative Importance of Meteorological and Aerosol-Related Parameters in Determining Cloud Microphysical Properties
Aerosol effects on cloud properties are notoriously difficult to disentangle from variations driven by meteorological factors. Here, a machine learning model is trained on reanalysis data and satellite retrievals to predict cloud microphysical properties, as a way to illustrate the relative importance of meteorology and aerosol, respectively, on cloud properties. It is found that cloud droplet effective radius can be predicted with some skill from only meteorological information, including estimated air mass origin and cloud top height. For ten geographical regions the mean coefficient of determination is 0.41 and normalised root-mean square error 24%. The machine learning model thereby performs better than a reference linear regression model, and a model predicting the climatological mean. A gradient boosting regression performs on par with a neural network regression model. Adding aerosol information as input to the model improves its skill somewhat, but the difference is small and the direction of the influence of changing aerosol burden on cloud droplet effective radius is not consistent across regions, and thereby also not always consistent with what is expected from cloud brightening
Converging organoids and extracellular matrix::New insights into liver cancer biology
Primary liver cancer, consisting primarily of hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA), is a heterogeneous malignancy with a dismal prognosis, resulting in the third leading cause of cancer mortality worldwide [1, 2]. It is characterized by unique histological features, late-stage diagnosis, a highly variable mutational landscape, and high levels of heterogeneity in biology and etiology [3-5]. Treatment options are limited, with surgical intervention the main curative option, although not available for the majority of patients which are diagnosed in an advanced stage. Major contributing factors to the complexity and limited treatment options are the interactions between primary tumor cells, non-neoplastic stromal and immune cells, and the extracellular matrix (ECM). ECM dysregulation plays a prominent role in multiple facets of liver cancer, including initiation and progression [6, 7]. HCC often develops in already damaged environments containing large areas of inflammation and fibrosis, while CCA is commonly characterized by significant desmoplasia, extensive formation of connective tissue surrounding the tumor [8, 9]. Thus, to gain a better understanding of liver cancer biology, sophisticated in vitro tumor models need to incorporate comprehensively the various aspects that together dictate liver cancer progression. Therefore, the aim of this thesis is to create in vitro liver cancer models through organoid technology approaches, allowing for novel insights into liver cancer biology and, in turn, providing potential avenues for therapeutic testing. To model primary epithelial liver cancer cells, organoid technology is employed in part I. To study and characterize the role of ECM in liver cancer, decellularization of tumor tissue, adjacent liver tissue, and distant metastatic organs (i.e. lung and lymph node) is described, characterized, and combined with organoid technology to create improved tissue engineered models for liver cancer in part II of this thesis. Chapter 1 provides a brief introduction into the concepts of liver cancer, cellular heterogeneity, decellularization and organoid technology. It also explains the rationale behind the work presented in this thesis. In-depth analysis of organoid technology and contrasting it to different in vitro cell culture systems employed for liver cancer modeling is done in chapter 2. Reliable establishment of liver cancer organoids is crucial for advancing translational applications of organoids, such as personalized medicine. Therefore, as described in chapter 3, a multi-center analysis was performed on establishment of liver cancer organoids. This revealed a global establishment efficiency rate of 28.2% (19.3% for hepatocellular carcinoma organoids (HCCO) and 36% for cholangiocarcinoma organoids (CCAO)). Additionally, potential solutions and future perspectives for increasing establishment are provided. Liver cancer organoids consist of solely primary epithelial tumor cells. To engineer an in vitro tumor model with the possibility of immunotherapy testing, CCAO were combined with immune cells in chapter 4. Co-culture of CCAO with peripheral blood mononuclear cells and/or allogenic T cells revealed an effective anti-tumor immune response, with distinct interpatient heterogeneity. These cytotoxic effects were mediated by cell-cell contact and release of soluble factors, albeit indirect killing through soluble factors was only observed in one organoid line. Thus, this model provided a first step towards developing immunotherapy for CCA on an individual patient level. Personalized medicine success is dependent on an organoids ability to recapitulate patient tissue faithfully. Therefore, in chapter 5 a novel organoid system was created in which branching morphogenesis was induced in cholangiocyte and CCA organoids. Branching cholangiocyte organoids self-organized into tubular structures, with high similarity to primary cholangiocytes, based on single-cell sequencing and functionality. Similarly, branching CCAO obtain a different morphology in vitro more similar to primary tumors. Moreover, these branching CCAO have a higher correlation to the transcriptomic profile of patient-paired tumor tissue and an increased drug resistance to gemcitabine and cisplatin, the standard chemotherapy regimen for CCA patients in the clinic. As discussed, CCAO represent the epithelial compartment of CCA. Proliferation, invasion, and metastasis of epithelial tumor cells is highly influenced by the interaction with their cellular and extracellular environment. The remodeling of various properties of the extracellular matrix (ECM), including stiffness, composition, alignment, and integrity, influences tumor progression. In chapter 6 the alterations of the ECM in solid tumors and the translational impact of our increased understanding of these alterations is discussed. The success of ECM-related cancer therapy development requires an intimate understanding of the malignancy-induced changes to the ECM. This principle was applied to liver cancer in chapter 7, whereby through a integrative molecular and mechanical approach the dysregulation of liver cancer ECM was characterized. An optimized agitation-based decellularization protocol was established for primary liver cancer (HCC and CCA) and paired adjacent tissue (HCC-ADJ and CCA-ADJ). Novel malignancy-related ECM protein signatures were found, which were previously overlooked in liver cancer transcriptomic data. Additionally, the mechanical characteristics were probed, which revealed divergent macro- and micro-scale mechanical properties and a higher alignment of collagen in CCA. This study provided a better understanding of ECM alterations during liver cancer as well as a potential scaffold for culture of organoids. This was applied to CCA in chapter 8 by combining decellularized CCA tumor ECM and tumor-free liver ECM with CCAO to study cell-matrix interactions. Culture of CCAO in tumor ECM resulted in a transcriptome closely resembling in vivo patient tumor tissue, and was accompanied by an increase in chemo resistance. In tumor-free liver ECM, devoid of desmoplasia, CCAO initiated a desmoplastic reaction through increased collagen production. If desmoplasia was already present, distinct ECM proteins were produced by the organoids. These were tumor-related proteins associated with poor patient survival. To extend this method of studying cell-matrix interactions to a metastatic setting, lung and lymph node tissue was decellularized and recellularized with CCAO in chapter 9, as these are common locations of metastasis in CCA. Decellularization resulted in removal of cells while preserving ECM structure and protein composition, linked to tissue-specific functioning hallmarks. Recellularization revealed that lung and lymph node ECM induced different gene expression profiles in the organoids, related to cancer stem cell phenotype, cell-ECM integrin binding, and epithelial-to-mesenchymal transition. Furthermore, the metabolic activity of CCAO in lung and lymph node was significantly influenced by the metastatic location, the original characteristics of the patient tumor, and the donor of the target organ. The previously described in vitro tumor models utilized decellularized scaffolds with native structure. Decellularized ECM can also be used for creation of tissue-specific hydrogels through digestion and gelation procedures. These hydrogels were created from both porcine and human livers in chapter 10. The liver ECM-based hydrogels were used to initiate and culture healthy cholangiocyte organoids, which maintained cholangiocyte marker expression, thus providing an alternative for initiation of organoids in BME. Building upon this, in chapter 11 human liver ECM-based extracts were used in combination with a one-step microfluidic encapsulation method to produce size standardized CCAO. The established system can facilitate the reduction of size variability conventionally seen in organoid culture by providing uniform scaffolding. Encapsulated CCAO retained their stem cell phenotype and were amendable to drug screening, showing the feasibility of scalable production of CCAO for throughput drug screening approaches. Lastly, Chapter 12 provides a global discussion and future outlook on tumor tissue engineering strategies for liver cancer, using organoid technology and decellularization. Combining multiple aspects of liver cancer, both cellular and extracellular, with tissue engineering strategies provides advanced tumor models that can delineate fundamental mechanistic insights as well as provide a platform for drug screening approaches.<br/
Forest planning utilizing high spatial resolution data
This thesis presents planning approaches adapted for high spatial resolution data from remote sensing and evaluate whether such approaches can enhance the provision of ecosystem services from forests. The presented methods are compared with conventional, stand-level methods. The main focus lies on the planning concept of dynamic treatment units (DTU), where treatments in small units for modelling ecosystem processes and forest management are clustered spatiotemporally to form treatment units realistic in practical forestry. The methodological foundation of the thesis is mainly airborne laser scanning data (raster cells 12.5x12.5 m2), different optimization methods and the forest decision support system Heureka. Paper I demonstrates a mixed-integer programming model for DTU planning, and the results highlight the economic advances of clustering harvests. Paper II and III presents an addition to a DTU heuristic from the literature and further evaluates its performance. Results show that direct modelling of fixed costs for harvest operations can improve plans and that DTU planning enhances the economic outcome of forestry. The higher spatial resolution of data in the DTU approach enables the planning model to assign management with higher precision than if stand-based planning is applied. Paper IV evaluates whether this phenomenon is also valid for ecological values. Here, an approach adapted for cell-level data is compared to a schematic approach, dealing with stand-level data, for the purpose of allocating retention patches. The evaluation of economic and ecological values indicate that high spatial resolution data and an adapted planning approach increased the ecological values, while differences in economy were small. In conclusion, the studies in this thesis demonstrate how forest planning can utilize high spatial resolution data from remote sensing, and the results suggest that there is a potential to increase the overall provision of ecosystem services if such methods are applied
Investigating the early interaction between Mycobacterium avium ssp paratuberculosis and the host using a bovine enteroid system
Mycobacterium avium ssp paratuberculosis (MAP) is the causative agent of Johneâs disease (JD), a chronic granulomatous enteritis of ruminantâs prevalent world-wide. Infection of calves occurs through the faecal oral route, typically in animals <6 months old. Animals are asymptomatic for 2-5 years before clinical signs begin to show, which typically present as emaciation and chronic diarrhoea. In the subclinical phase, animals will have decreased milk yield, increased susceptibility to other diseases and decreased feed conversion. This has a severe impact on the farming economy and animal welfare, as affected animals are often prematurely culled.
Infected subclinical animals are extremely difficult to identify but can still act as a source of transmission for the rest of the herd by shedding MAP in their faeces. There is no treatment for JD, and the current diagnostic tests are ineffective. By investigating the initial interaction between MAP and the host at the intestinal lining, a greater understanding of MAP pathogenesis can be gained and better diagnostic and therapeutic targets can be identified.
In this work, proteins expressed on the surface of MAP were assessed for their ability to aid attachment, invasion and intracellular survival in epithelial and phagocytic cells when expressed on the membrane of a non-invasive E. coli host strain. The proteins investigated were encoded by mammalian cell entry (mce) genes, mce1A, mce1D, mce3C and mce4A, which have been implicated in attachment and invasion of epithelial cells by other mycobacteria. Interestingly, E. coli expressing Mce1A had enhanced uptake by phagocytic cells and E. coli expressing Mce1D had enhanced attachment and invasion of epithelial cells, but neither protein conferred this phenotype in both eukaryotic cell types investigated.
To identify key intestinal cell types involved in MAP pathogenesis, bovine intestinal organoids (enteroids) were assessed for their ability to model a MAP infection in a physiologically representative system. Baso-out 3D enteroids, apical-out 3D enteroids and 2D monolayers were created, and the cell types present were compared to bovine intestinal tissue samples using RT-PCR and immunofluorescence microscopy. The models contained the mature epithelial cell types of the intestine including goblet cells, enteroendocrine cells, Paneth cells and enterocytes. 3D baso-out enteroids and 2D
monolayers also contained proliferative cells, but the 3D apical-out enteroids did not and so could not be maintained past 2 weeks of culture.
The models were infected with two strains of MAP over the course of 72 hours, the reference strain K10, and a recent clinical isolate C49. MAP C49 was shown to be present in all three intestinal models in consistently higher numbers than MAP K10, quantified using qPCR of the genomic DNA. This indicates that MAP C49 was better able to infect these models than K10, which may suggest a loss of virulence in MAP K10.
Overall, the data presented has increased our understanding of MAP pathogenesis by emphasising the need for multicellular models which accurately represent the pathogen target cell type/s in vivo and the confirmation of the role of two hypothetical MAP proteins in cellular interactions
Archaeological palaeoenvironmental archives: challenges and potential
This Arts and Humanities Research Council (AHRC) sponsored collaborative doctoral project represents one of
the most significant efforts to collate quantitative and qualitative data that can elucidate practices related to
archaeological palaeoenvironmental archiving in England. The research has revealed that archived
palaeoenvironmental remains are valuable resources for archaeological research and can clarify subjects that
include the adoption and importation of exotic species, plant and insect invasion, human health and diet, and
plant and animal husbandry practices. In addition to scientific research, archived palaeoenvironmental remains
can provide evidence-based narratives of human resilience and climate change and offer evidence of the
scientific process, making them ideal resources for public science engagement. These areas of potential have
been realised at an imperative time; given that waterlogged palaeoenvironmental remains at significant sites
such as Star Carr, Must Farm, and Flag Fen, archaeological deposits in towns and cities are at risk of decay due
to climate change-related factors, and unsustainable agricultural practices. Innovative approaches to collecting
and archiving palaeoenvironmental remains and maintaining existing archives will permit the creation of an
accessible and thorough national resource that can service archaeologists and researchers in the related fields
of biology and natural history. Furthermore, a concerted effort to recognise absences in archaeological
archives, matched by an effort to supply these deficiencies, can produce a resource that can contribute to an
enduring geographical and temporal record of England's biodiversity, which can be used in perpetuity in the
face of diminishing archaeological and contemporary natural resources.
To realise these opportunities, particular challenges must be overcome. The most prominent of these include
inconsistent collection policies resulting from pressures associated with shortages in storage capacity and
declining specialist knowledge in museums and repositories combined with variable curation practices. Many of
these challenges can be resolved by developing a dedicated storage facility that can focus on the ongoing
conservation and curation of palaeoenvironmental remains. Combined with an OASIS + module designed to
handle and disseminate data pertaining to palaeoenvironmental archives, remains would be findable,
accessible, and interoperable with biological archives and collections worldwide. Providing a national centre for
curating palaeoenvironmental remains and a dedicated digital repository will require significant funding.
Funding sources could be identified through collaboration with other disciplines. If sufficient funding cannot be
identified, options that would require less financial investment, such as high-level archive audits and the
production of guidance documents, will be able to assist all stakeholders with the improved curation,
management, and promotion of the archived resource
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