Gotowe bibliografie tematyczne / Forensic taphonomy

Gotowa bibliografia na temat „Forensic taphonomy”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 29 lipca 2024

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Artykuły w czasopismach na temat "Forensic taphonomy"

Bartelink, Eric J. "Review of:Manual of Forensic Taphonomy". Journal of Forensic Sciences 59, nr 4 (27.06.2014): 1164. http://dx.doi.org/10.1111/1556-4029.12497.

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İşcan, Mehmet Yaşar, i Barbara Q. McCabe. "Forensic Taphonomy: The Postmortem Fate of Human Remains". Forensic Science International 116, nr 2-3 (luty 2001): 227–28. http://dx.doi.org/10.1016/s0379-0738(00)00376-5.

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Duhig, C. "Non-forensic remains: the use of forensic archaeology, anthropology and burial taphonomy". Science & Justice 43, nr 4 (październik 2003): 211–14. http://dx.doi.org/10.1016/s1355-0306(03)71778-x.

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Miles, Kelly L., Devin A. Finaughty i Victoria E. Gibbon. "A review of experimental design in forensic taphonomy: moving towards forensic realism". Forensic Sciences Research 5, nr 4 (13.08.2020): 249–59. http://dx.doi.org/10.1080/20961790.2020.1792631.

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Milroy, C. M. "Book: Forensic Taphonomy: The Postmortem Fate of Human Remains". BMJ 319, nr 7207 (14.08.1999): 458. http://dx.doi.org/10.1136/bmj.319.7207.458.

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Ioan, Beatrice Gabriela, Cristiana Manea, Bianca Hanganu, Laura Statescu, Laura Gheuca Solovastru i Irina Manoilescu. "The Chemistry Decomposition in Human Corpses". Revista de Chimie 68, nr 6 (15.07.2017): 1352–56. http://dx.doi.org/10.37358/rc.17.6.5672.

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Human body is a complex of organic substances (proteins, lipids, carbohydrates), which undergo chemical decomposition processes soon after death. The compounds released during decomposition characterize the development of different stages of this process: e.g. biogenic amines resulted from the proteins decomposition will confer the particular smell of a cadaver, gases resulted from carbohydrates fermentation will give the bloating aspect of the cadaver. The study of cadaver decomposition and the products resulted from this process is the subject of human taphonomy and is realized nowadays in special facilities in USA and Australia. Identification and analysis of the chemical compounds emerged after human decomposition (gases, liquids, salts) give valuable information to forensic pathologists for estimating the postmortem interval (PMI). More, volatile compounds � which give the odor signature�specific to human remains � may be utilized in identifying clandestine burials, human remains or victims entrapped under ruins in cases of natural disasters. In this paper the authors describe the chemical decomposition stages of human cadavers, the factors influencing these processes and utility for the forensic activity of the results of human taphonomic studies.

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Rowe, Walter F. "Review of:Advances in Forensic Taphonomy: Method, Theory, and Archaeological Perspectives". Journal of Forensic Sciences 47, nr 6 (1.11.2002): 15590J. http://dx.doi.org/10.1520/jfs15590j.

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Dirkmaat, Dennis C., i Luis L. Cabo. "Forensic Archaeology and Forensic Taphonomy: Basic Considerations on how to Properly Process and Interpret the Outdoor Forensic Scene". Academic Forensic Pathology 6, nr 3 (wrzesień 2016): 439–54. http://dx.doi.org/10.23907/2016.045.

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Spies, Maximilian J., Victoria E. Gibbon i Devin A. Finaughty. "Forensic taphonomy: Vertebrate scavenging in the temperate southwestern Cape, South Africa". Forensic Science International 290 (wrzesień 2018): 62–69. http://dx.doi.org/10.1016/j.forsciint.2018.06.022.

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Iqbal, Mohammad Asif, Maiken Ueland i Shari L. Forbes. "Recent advances in the estimation of post-mortem interval in forensic taphonomy". Australian Journal of Forensic Sciences 52, nr 1 (9.05.2018): 107–23. http://dx.doi.org/10.1080/00450618.2018.1459840.

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Rozprawy doktorskie na temat "Forensic taphonomy"

Rogers, Christopher. "Dating death : forensic taphonomy and the postmortem interval". Thesis, University of Wolverhampton, 2010. http://hdl.handle.net/2436/210852.

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Determining the postmortem interval (PMI) remains one of the most important but challenging factors to establish in a suspicious death investigation. Unfortunately, as time passes current methods lose accuracy and only allow investigators to approximate how long ago death occurred. Bodies interred in clandestine graves prove particularly challenging due to an abundance of variables that need to be taken into consideration. Due to the problems associated with determining the PMI of buried remains this study will utilise macroscopic, microscopic, molecular, chemical and microbiological analyses to systematically document the decompositional changes to human hair and porcine cartilage and bone in a burial environment. The aim was to correlate decompositional changes with time and develop new methods for estimating the PMI of remains found in this context. Whole trotters (from which the cartilage was harvested) exhibited decompositional changes including darkening of the dermis, skin slippage, liquefaction of soft tissues and complete skeletonisation. The decompositional changes to cartilage included a loss of cartilage covering articular facets, changes in colour and texture, formation of orthorhombic crystals, a change in surface pH and colonisation by bacteria. The bacteria found on the cartilage surface were in close proximity to the crystals and when cultured on a B-41 medium were found to precipitate crystals of the same morphology and chemical composition to those found on the cartilage surface. Three species of bacteria (Acinetobacter calcoaceticus, Acinetobacter iwoffii and Grimontia hollisae) were identified based on gas chromatography–mass spectrometry (GC-MS) of their fatty acids and one species (Comamonas sp.) was identified by DNA analysis. Formation of crystals on goat and cow cartilage proved that this was not a porcine specific phenomenon. Human hair exhibited a gradual degradation over time but this was dependent on the characteristics of the burial environment. Decompositional changes included colonisation by fungi, erosions to the cortical surface and formation of tunnels and breaks to the hair shaft. Two fungal species (Aspergillus fumigatus and Penicillium sp.) were identified based on DNA analysis of fungal ribosomal (rDNA) internally transcribed spacer (ITS) regions. The Penicillium sp. was linked with fungal tunnelling of hair. Bone exhibited little modification over time but changes were observed. These included a change in colour of the cortical surface, a change in colour and gradual loss of bone marrow and erosions, cracking and flaking of the cortical bone. Fungi were found to colonise both the bone marrow and bone surface. Whole piglets were buried to document the time period taken to reach skeletonisation. This data was used as a correction factor and combined with the bone results to give an overall time period for the decomposition changes observed. The results of this study suggest that the decompositional changes to cartilage could be used to determine the postmortem interval of buried remains. However, the degradation of hair and bone was too variable to be of use in this context.

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Haglund, William D. "Applications of taphonomic models to forensic investigations /". Thesis, Connect to this title online; UW restricted, 1991. http://hdl.handle.net/1773/6424.

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Bolton, Shawna N. "Forensic taphonomy : investigating the post mortem biochemical properties of cartilage and fungal succession as potential forensic tools". Thesis, University of Wolverhampton, 2015. http://hdl.handle.net/2436/579577.

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Post mortem interval (PMI – the time elapsed since death and discovery) is important to medicolegal investigations. It helps to construct crucial time lines and assists with the identification of unknown persons by inclusion or exclusion of a suspect’s known movements. Accurate methodologies for establishing PMI are limited to about 48-hours. Such methods involve use of increasing levels of potassium in vitreous humour, and algor mortis. This study is two-fold. Firstly, it explores the biomolecular changes in degrading porcine cartilage buried in soil environments and its potential to determine PMI in the crucial two days to two months period. Trotters were interred in a number of graves at two distinct locations exhibiting dissimilar soil environments. Weekly disinterments (for 6 weeks) resulted in dissection for cartilage samples which were processed for protein immunoblot analyses and cell vitality assays. Results demonstrate that aggrecan, a major structural proteoglycan, produces high (230kDa) and low (38kDa) molecular weight cross-reactive polypeptides (CRPs) within cartilage extracellular matrix. The 230kDa CRP degrades in a reproducible manner irrespective of the different soil environments utilised. As PMI increases, aggrecan diminishes and degrades forming heterogeneous subpopulations with time. Immunodetection of aggrecan ceases when joint exposure to the soil environment occurs. At this time, aggrecan is metabolised by soil microbes. The molecular breakdown of cartilage proteoglycans has potential for use as a reliable indicator of PMI, irrespective of differing soil environments, beyond the 48-hours period. Likewise, vitality assays also demonstrated viable chondrocytes for as long as 35 PM days. The second component of this study examined the fungal activity associated with trotters buried below ground. Results indicate that fungal growth was considerably influenced by soil chemistry and changes in the environment. Fungal colonisation did not demonstrate temporal patterns of succession. The results of this study indicate that cartilage has the potential to prolong PMI determination well beyond the current 48- and 100-hour limitations posed by various other soft tissue methods. Moreover, the long-term post mortem viability of chondrocytes presents an opportunity to explore DNA extraction from these cells for the purpose of establishing a positive identification for unidentified remains. On the contrary, the growth and colonisation patterns of post putrefactive fungi in relation to decomposing porcine trotters proved to be futile for estimating PMI. Therefore, fungi may not be a suitable candidate for evaluating PMI during the early phase fungal activity.

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Stokes, Kathryn Lisa. "Soil-cadaver interactions in a burial environment". University of Western Australia. Faculty of Life and Physical Sciences, 2009. http://theses.library.uwa.edu.au/adt-WU2009.0065.

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Forensic taphonomy is concerned with investigation of graves and grave sites. The primary aim of forensic taphonomy is development of accurate estimations of postmortem interval (PMI) and/or postburial interval (PBI). Soil has previously been largely ignored, therefore this thesis is designed to investigate changes in decomposition as imparted by the soil. Furthermore the impact of cadaver interment on the surrounding soil may offer prospects for identification of clandestine graves. A series of laboratory controlled decomposition experiments using cadavers (Mus musculus) and cadaver analogues (skeletal muscle tissue (SMT); Sus scrofa, Homo sapiens, Ovis aries and Bos Taurus) were designed to investigate decomposition in burial environments. Sequential destructive harvests were carried out to monitor temporal changes during decomposition. Analyses conducted included; mass loss, microbial activity (CO2 respiration) and soil chemistry (pH, EC and extractable NH4 +, NO3 -, PO4 3- and K+). Several experimental variables were tested; frozen-thawed versus refrigerated SMT, different mammalian sources of SMT, different soil type and contribution of soil versus enteric microbial communities. Mass loss measurements for SMT experiments demonstrated a sigmoidal pattern of mass loss, however, larger cadavers (Mus musculus, 5 weeks) did not. The inhumation of SMT (frozen, unfrozen, different mammalian sources) or cadavers leads to an increase in microbial activity (CO2 respiration) within 24 hours of burial. A peak of microbial activity is attained within a week, followed by a decrease and eventual plateau. The rapid influx in microbial activity is matched by corresponding increases in pH and NH4 + concentration. pH and NH4 + are strongly correlated in soils with acidic basal pH, by comparison highly alkaline soil demonstrated no relationship. NH4 + concentration also appeared to be related directly to NO3 - concentration and cadaver or SMT mass. A decrease in NH4 + corresponds with an increase in NO3 -, however, nitrification was unpredictable. Rapid nitrification was observed in sand systems when SMT was interred, but was not noted when cadavers were interred. By comparison both sandy clay loam and loamy sand soils demonstrated rapid nitrification after inhumation of a cadaver. When cadaver or cadaver analogue mass was larger, so were NH4 + and NO3 - concentrations in systems that experienced nitrification.

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Griffiths, Samuel John. "Aquatic bone taphonomy : forensic and archaeological implications for the interpretation of submerged bone". Thesis, University of Southampton, 2018. https://eprints.soton.ac.uk/423819/.

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There is currently an incomplete understanding of the effects that aquatic processes have on skeletal material, and consequently the interpretation of water-submerged remains presents a number of challenges to archaeologists and forensic practitioners. Accurate interpretations of the conditions which cause diagnostic diagenetic changes to material are not just important for reconstructing post-depositional environments, processes and durations, but are also vital in ensuring that any data recovered from bone are not incorrectly interpreted due to information loss and modification. This thesis therefore addresses the paucity in data concerning early postdepositional modifications in submerged bone, by exploring different methods and analyses that facilitate more accurate interpretations of bones’ aquatic diagenetic and taphonomic pathways. A number of experimental and actualistic bone taphonomy studies are presented and discussed. A series of laboratory flume-based experiments demonstrate the utility of quantitative analysis of sediment-induced micro- abrasion on bone surfaces. SEM imaging allowed quantitative and qualitative distinctions to be made concerning the sediment size class that the bone was abraded by. Changes in sediment grain size, duration of exposure to abrasion, sphericity of the abrasive, and abrasive force are identified as the strongest rate-limiting factors controlling micro-abrasion propagation. Through this data it is suggested that a quantitative approach to analysing abrasion on bone retrieved from water has potential to establish remains’ submersion times and transport pathways with a higher degree of resolution than previously possible. The use of laser scanning for quantitatively recording sediment abrasion on submerged bone is also explored. Point cloud analysis was carried out, and it is shown that laser scanning can be used to accurately record abrasion on submerged bone at a resolution not possible through gross morphological assessment. It is therefore suggested that this quantitative approach facilitates an improved assessment of abrasive changes recorded on bone in experimental and actualistic taphonomy studies. Finally, a series of early-post-depositional monitoring studies were conducted in field and laboratory-based settings to assess both predictability and rates of diagenetic change as they relate to different spatio-temporal parameters of submersion. A suite of physicochemical changes in bone, recorded using gross morphological observations, histological assessments of bone microstructure, DNA analysis, FTIR-ATR analysis of bones’ mineral and organic constituents, quantitative measures of colour change using VSC analysis, and XRF analysis of bones’ elemental compositions, are discussed. The key findings of this study are that microbial modification in submerged osseous tissue can progress rapidly upon deposition in water and have the ability to propagate into cortical tissue, which may impact on the ability of remains to survive over archaeological and palaeontological time periods. Elemental exchange rates in submerged bone are identified as the most consistent markers of post-depositional change at both site-specific and broader scales. Remains that were constantly buried in bottom sediments and exhibit good gross morphological and histological integrity displayed notably consistent elemental uptake and depletion rates, which suggests they have utility for determining remains’ submersion times and locations. DNA degradation is shown to be rapid in submerged bone due to the effects of hydrolysis. It is also indicated that remains which experienced burial and exhibit limited microstructural changes are likely to show better retention of residual biomolecules and are therefore favourable to target for DNA analysis. This thesis concludes that a quantitative approach to recording both intrinsic and extrinsic variables related to bone diagenesis is advantageous for understanding taphonomic effect, cause and duration, and should therefore be adopted in future studies. In addition, this research provides a good fundamental basis concerning the occurrence and progression of different diagenetic changes in water-submerged remains, on which additional studies can build.

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O'Brien, R. Christopher. "Forensic animal necrophagy in the South-West of Western Australia : species, feeding patterns and taphonomic effects". University of Western Australia. School of Anatomy and Human Biology, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0195.

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[Truncated abstract] One of the standard ways of assessing time since death is from the stages of decomposition of the body. It is well known that the rate of decomposition is affected by environmental factors such as temperature and humidity. Another factor that can affect decompositional rates is the presence of breaches in the protective barrier of the skin, whether arising from antemortem injury or postmortem damage, including that occurring from animal necrophagy. Scavengers have the potential to affect decomposition by breaching the skin allowing access to associated insect material, feeding on the maggot masses, or by consumption of the carcass itself. Each locality will have its own set of features determining the rate of decomposition of the body, and variation may occur within localities based on the seasons. Such variation implies the need for local calibration of time since death against degree of decomposition and to establish the magnitude of interseasonal variation. When the localities are outdoors, the influence of potential scavengers, and the factors affecting their activity need also to be taken into account. This study investigates the interaction of environmental factors and animal scavenging on the rate of decomposition of pig (Sus scrofa) carcasses at four south-west Western Australia sites; Jandakot, Shenton Park, Perup Forest, and Watheroo National Park. Jandakot and Shenton Park are both close to the Perth metropolitan area and the western coast while Perup Forest is southern and inland and Watheroo is northern and inland. ... The most common insectivore feeding in relation to the carcasses was the Willie Wagtail (Rhipidura leucophrys) which was associated with the carcasses in all seasons and all locations except for Perup Forest. The breeding cycle appeared to have a marked influence on the intensity of scavenging by several species. The effect of season on decompositional rates was greatly reduced in carcasses that were exposed to scavenging. It took no additional time for carcasses to achieve skeletonization in winter than in the other seasons in the presence of scavenging. Scavenging had no significant impact on the rate of breakdown of carcasses in summer, when decompositional rates were greatest and scavenging at a minimum. v In Western Australia, it is not uncommon for bodies to remain undiscovered in bush environments for lengthy periods of time due to the low human population density. This study shows conclusively that it is not sufficient simply to consider the accumulated degree day (ADD) when estimating time since death by the degree of decomposition of the body. Attention must also be given to local wildlife assemblages and variations in their activities with the seasons. The implications of this research are in the determination of time of death. If the effects of scavengers accelerate decomposition this must be taken into account when any calculation since time of death is determined. The marked variations between sites in the rates of decomposition of carcasses exposed to natural animal scavenging in this study highlights the need for local calibration of time since death to decompositional stages for all locales. The techniques devised in this study are straight forward and easily conducted yet are informative and essential in determining time since death for bodies which have been exposed to animal scavenging.

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Parsons, Hillary Renee. "The postmortem interval a systematic study of pig decomposition in West Central Montana /". Diss., [Missoula, Mont.] : The University of Montana, 2009. http://etd.lib.umt.edu/theses/available/etd-06192009-183725.

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Cappella, A. "INTERPRETATION OF TRAUMA AND TAPHONOMY IN A MODERN KNOWN SKELETAL POPULATION: IMPLICATION FOR FORENSIC ANTHROPOLOGY". Doctoral thesis, Università degli Studi di Milano, 2015. http://hdl.handle.net/2434/253377.

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In Forensic Anthropology, trauma analysis is essential for a correct understanding of the cause and the modality of death as well as for the interpretation of previous traumatic events which occurred in life. Both have important implications in criminal and humanitarian scenarios: to demonstrate whether a crime was committed, and to ascertain torture and maltreatment. Nevertheless, the assessment of a traumatic event, whether antemortem, perimortem or potmortem, is extremely challenging and often limited and altered by multiple variables, namely taphonomy. Few are the validated scientific methods which can help anthropologists in the interpretation of skeletal trauma, and which are often limited by the lack of known skeletal material on which to conduct research in order to acquire data, to validate methods and to study and create theoretical trauma and taphonomy models. Among the many known documented skeletal collections already presented officially to the international scientific community very few are equipped also with known/control data on trauma, and cause and modality of death. The Milan cemeterial Skeletal Collection, which is only part of the more consistent Milan Osteological Skeletal Collection housed at LABANOF (University of Milan) is one of the latter, and its presence has offered the chance to conduct research on the difficult field of trauma and taphonomy included in the Ph.D project. The first ever anthropological study of the skeletal sample of the Milan skeletal collection here presented, has been the starting point which permitted us to highlight the numerous diagnostic difficulties concerning trauma analysis and has provided the material on which to conduct the applied research for analysing the state of the art currently used by the discipline. As a consequence of the many limits arising from the first two research lines (on the diagnosis of antemortem lesions as well as the identification of perimortem injury), which appeared not satisfactory enough for a correct interpretation of skeletal lesions, the research has focused on the novel field of blood taphonomy in order to provide knowledge for the use of cell components and biomarkers as indicators of vitality and survival on skeletal trauma which represents more reliable future possible alternative solutions.

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Barker, Andrew Lewis. "Mass Spectrometry-Based Identification of Ceramic-Bound Archaeological Protein Residues: Method Validation, Residue Taphonomy, and Prospects". Thesis, University of North Texas, 2018. https://digital.library.unt.edu/ark:/67531/metadc1404522/.

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Despite the variety of successful reports of the preservation, recovery, and identification of archaeological proteins in general, there are few positive reports regarding mass spectrometry-based identification of ceramic-bound proteins. In large part, this shortage is due to the lack of consideration for the unique taphonomic histories of such residues and, in general, methods development. Further, because negative results are rarely published, there is no baseline to which results can be compared. This paper attempts to address these challenges via a multi-pronged approach that uses mass spectrometry and complementary approaches to evaluate ceramic-bound protein preservation in both controlled, actualistic experiments, and in archaeological artifacts. By comparing the results obtained from protein-spiked, experimentally-aged ceramic to those obtained from both faunal and ceramic archaeological materials, an enhanced perspective on protein preservation and subsequent recovery and identification is revealed. This perspective, focusing on taphonomy, reveals why negative results may be the norm for ceramic artifacts when non-targeted methods are employed, and provides insight into how further method development may improve the likelihood of obtaining positive results.

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Luitingh, Taryn Leigh. "Adaptation of the microbial decomposer community to the burial of skeletal muscle tissue in contrasting soils". University of Western Australia. Centre for Forensic Science, 2008. http://theses.library.uwa.edu.au/adt-WU2009.0037.

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Microorganisms are known to be agents involved in the decomposition of organic matter. However, little is known about the participation of the microbial communities during the decomposition of mammalian skeletal muscle tissue. This study investigates the capacity of the soil microbial community to adapt to the decomposition of skeletal muscle tissue in differing soils. This has implications for the study of mass graves and sites of repeated burial. A controlled laboratory experiment was designed to assess the adaptability of microbial communities present in three distinct soil types (sand, loamy sand and sandy clay loam) found near Perth, Western Australia. This experiment was split into two main stages. The initial decomposition stage involved the addition of porcine skeletal muscle tissue (SMT) (Sus scrofa) to each of the three soil types which were then left to decompose for a period of time. Controls were run in parallel, which had no porcine SMT present. The second decomposition stage involved a second addition of SMT to the soils obtained from the initial decomposition stage. Therefore, for each soil, SMT was either decomposed in the soil that had been pre-exposed to SMT or not. The rate of decomposition, microbial activity (CO2 respiration) and microbial biomass (substrate-induced respiration) were monitored during the second decomposition stage. The functional diversity of the microbial populations in the soil were assessed using Community-Level Physiological Profiling (CLPP). Across the three soil types, the re-introduction of SMT to the soil has led to its enhanced decomposition (measured by tissue mass loss and microbial activity) by the microbial communities. This microbial adaptation may have been facilitated by a functional change in the soil microbial communities.

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Książki na temat "Forensic taphonomy"

Pokines, James T., Ericka N. L’Abbé i Steven A. Symes. Manual of Forensic Taphonomy. Wyd. 2. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.4324/9781003171492.

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Mata, Alejandro Terrazas. Tafonomía, medio ambiente y cultura: Aportaciones a la antropología de la muerte. México, D.F: Universidad Nacional Autónoma de México, Instituto de Investigaciones Antropológicas, 2007.

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DiNovo, Amanda B. Forensic taphonomy and its relationship with soil. [San Diego, California]: National University, 2013.

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D, Haglund William, i Sorg Marcella H, red. Advances in forensic taphonomy: Method, theory, and archaeological perspectives. Boca Raton, Fla: CRC Press, 2002.

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D, Haglund William, i Sorg Marcella H, red. Forensic taphonomy: The postmortem fate of human remains. Boca Raton: CRC Press, 1997.

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Haglund, William D. Applications of taphonomic models to forensic investigations. [Seattle, Wash.]: [s.n.], 1991.

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Schotsmans, Eline M. J., Nicholas Márquez-Grant i Shari L. Forbes, red. Taphonomy of Human Remains: Forensic Analysis of the Dead and the Depositional Environment. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781118953358.

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Sorg, Marcella H., i William D. Haglund, red. Forensic Taphonomy. CRC Press, 1996. http://dx.doi.org/10.1201/9781439821923.

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Pokines, James T., Steven A. Symes i Ericka N. L'Abbe. Manual of Forensic Taphonomy. Taylor & Francis Group, 2021.

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Pokines, James T., Steve A. Symes i Ericka N. LAbbé. Manual of Forensic Taphonomy. Taylor & Francis Group, 2021.

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Części książek na temat "Forensic taphonomy"

Schneider, Carrington S., James T. Pokines, Ericka N. L’Abbé i Briana Pobiner. "Reptile Taphonomy". W Manual of Forensic Taphonomy, 667–94. Wyd. 2. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.4324/9781003171492-19.

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Evans, Thomas. "Fluvial Taphonomy". W Manual of Forensic Taphonomy, 163–92. Wyd. 2. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.4324/9781003171492-06.

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Pokines, James T., Stephanie Edwards Baker i Corey Pollock. "Avian Taphonomy". W Manual of Forensic Taphonomy, 581–604. Wyd. 2. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.4324/9781003171492-16.

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Sorg, Marcella H., William D. Haglund i Jamie A. Wren. "Current Research in Forensic Taphonomy". W A Companion to Forensic Anthropology, 477–98. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118255377.ch24.

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Bristow, Joanne, Zoe Simms i Patrick Randolph-Quinney. "Taphonomy". W Forensic Anthropology, 279–317. Taylor & Francis, 2011. http://dx.doi.org/10.1201/b10727-10.

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Christensen, Angi M., Nicholas V. Passalacqua i Eric J. Bartelink. "Forensic Taphonomy". W Forensic Anthropology, 119–47. Elsevier, 2014. http://dx.doi.org/10.1016/b978-0-12-418671-2.00005-7.

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Nienaber, Coen, Shari L. Forbes, Melissa Connor, Daniel J. Wescott, Jodie Ward, Dawnie W. Steadman i Kerri L. Colman. "Forensic Taphonomy". W Encyclopedia of Forensic Sciences, Third Edition, 700–711. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-12-823677-2.00040-4.

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Christensen, Angi M., i Nicholas V. Passalacqua. "Forensic Taphonomy". W A Laboratory Manual for Forensic Anthropology, 71–83. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-812201-3.00005-0.

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Rattenbury, Amy E. "Forensic Taphonomy". W Forensic Ecogenomics, 37–59. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-809360-3.00002-3.

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Simmons, T., i P. A. Cross. "Forensic Taphonomy". W Encyclopedia of Forensic Sciences, 12–17. Elsevier, 2013. http://dx.doi.org/10.1016/b978-0-12-382165-2.00004-0.

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Streszczenia konferencji na temat "Forensic taphonomy"

Bacci, Nicholas, Tanya Augustine, Patrick Randolph-Quinney, Hugh Hunt i Ken Nixon. "Recognition of lightning-induced trauma to the skeleton: A forensic taphonomic study". W 2014 International Conference on Lightning Protection (ICLP). IEEE, 2014. http://dx.doi.org/10.1109/iclp.2014.6973330.

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