Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Student Name: _____Maria Alice Ciobanu______________________ Student ID:_____ 3395606__________________________ Blood evidence Part 1: Physiology of Blood (30%of Mark) Q) Name and describe in detail the three main formed elements in blood The red blood cells (erythrocytes) account for 99% of formed elements. In most mammals mature erythrocytes are biconcave discs that have no nuclei. The cell consists mostly of haemoglobin and stroma. The amount of the erythrocytes contained by adult human blood is 4.5-5.8 x 1011 per decilitre. Due to their ability to deform shape, they can pass through capillaries in the peripheral circulation, although they have approximately 8 µm in diameter. Erythrocyte formation (erythropoiesis) takes place in the bone marrow in the adult, and in the liver, spleen and bone marrow of the fetus. After 120 days in the circulation they are removed by the reticulo-endothelial system of the spleen and liver. The main functions are the transport of oxygen from the lungs to the tissue, the maintenance of blood pH and to facilitate the buffering capacity of blood (Russell et al 1982). The leucocytes (white blood cells) represent about 1%volume of formed elements. Blood contains approximately 7.5 x 108 white cells per decilitre, their size varying between 1020µm in diameter. Five types of leucocytes are classified by the presence or absence of granules in the cytoplasm of the cell; the agranulocytes (lymphocytes and monocytes) and the granulocytes (neutrophils, basophils and eosinophils). Their overall lifespan is probably a few days and they are concerned with the immune response of the body, acting as phagocytes, detoxifiers and immune system cells. The defence of the body is realized by the B lymphocytes which produce antibodies and T lymphocytes which participate in various cellular immune reactions (Russell et al 1982). Comprising 0.5 per cent of the blood volume, platelets are small blood cells which are synthesized in the bone marrow from megakaryocytes. Thrombocytes are not nucleated, but they contain large numbers of membrane-enclosed granules and dense bodies with a high affinity for collagen and elastin fibres and adhere to them at the site of vessel-wall damage in order to prevent blood-loss. These disc shaped blood cells have a diameter of 2 to 4 µm playing a crucial role into clotting mechanism of blood (Russell et al 1982). Part Two: Blood testing (30% of Mark) Q) Describe in detail a test that can be used for the detection of trace blood? The base of the presumptive tests is represented by the ability of the haemoglobin existent in erythrocytes to catalyse the oxidation of certain reagents. The most commonly used reagent is phenolphthalein, which in its reduced form is colourless but purple/fuchsia coloured in the oxidised state. Colour-change tests are able to identify minute amounts of blood, for example in cracks in the walls and floors. Forensic analysts use the Kastle Mayer test usually for determining if the composition of a stain contains blood before carrying out other more complicated blood-specific test. However, this presumptive test has its disadvantages due to the fact that phenolphthalein cannot distinguish between human blood, other animal blood or vegetable peroxidases (James and Nordby, 2005). Q) Describe in detail the precipitin test for blood The precipitin test is based on an antibody-antigen complex, in order for the origin of a bloodstain to be determined whether it is human or animal. This test utilizes simple diffusion between an antiserum and an extract from the bloodstain in a test tube. If the blood is human, dissolved antigens and antibodies from the antiserum layer will start to diffuse into the other layer, resulting into a fine line of precipitate on the interface of the two solutions. No reaction will be visible if the extract is animal (James and Nordby, 2005). Q) Describe the theoretical principles of the ABO blood typing system. In order for a human origin bloodstain to be associated with a particular individual, ABO blood typing system represents a serological technique of a great ability in the field of Page 1 of 3 Student Name: _____Maria Alice Ciobanu______________________ Student ID:_____ 3395606__________________________ forensic analysis. This human antigenic system is based on the existence or the absence of antigens on the surface of the erythrocytes and corresponding antibody within the blood plasma. Therefore, an agglutination reaction which will bind the red cells together will occur if an individual receives the incorrect blood group. Forensic testing for the presence of antibodies commonly uses the absorption-elution for antigenic characteristics and the Lattes Crust test (White, 2005). Part 3: The effect of angle on blood splatter shape (40% of Mark) Calculations: Using the equation provided below, calculate the angle of the six blood drops. Width: 4mm Blood drop one Blood drop two Length: 6mm Width: 3mm Blood drop four Angle 41.81 Angle 14.47 Width: 9mm Width: 7mm Length: 9mm Blood drop five Angle 90 Width: 2mm Blood drop three: Length: 12mm Length: 7mm Length: 9mm Angle 51.05 Width: 5mm Blood drop six Length: 25mm Angle 16.60 Angle 11.53 Q) Describe in detail the principles of ‘Cast-off’ blood pattern analysis Cast-off patterns represent the effect produced by blood when it is released or thrown from a secondary moving object that is soaked with blood. In order for a cast-off bloodstain pattern to be formed, the centrifugal force generated by a swinging bloodied object needs to be sufficiently great to overcome the adhesive force that holds the blood to the weapon. An important characteristic of this pattern is the linear distribution of individual drops of blood, which may appear curved or straight depending on the circumstances of its deposition. Also it can be ascertain the direction in which droplets of blood were travelling when they hit adjacent surfaces and the relative positions of the victim and suspect. Furthermore, information about the type of the instrument used in the attack and the number of blows struck can be revealed when carefully examining cast-off bloodstains. (James and Nordby, 2005) Q) Describe in detail the effect of force on the formation of blood splatter When sufficient force is available to overcome the surface tension of blood, spatter is created. The resulting bloodstains vary considerably with gunshot, stabbing or beating events. Therefore, if the force applied has a low velocity impact\force (1.5m\s), the diameter of blood droplets are typically greater than 3 mm, depending also on the availability of the exposed blood. Impact spatter associated with stabbing and blunt force (medium velocity impact\force) is around 1.5-7m\s and generally exhibits a size range from 1 to 3 mm in diameter. When the misting effect is observed or satellite spatter is produced by blood, they usually are associated with gunshot, explosions and high-speed machinery impact. If associated with an entrance wound, back spatter can be observed. The force applied in this case can reach 30m\s or more, exhibiting a wide size range from less than 1 mm in diameter. (Pepper, 2005) Page 2 of 3 Student Name: _____Maria Alice Ciobanu______________________ Student ID:_____ 3395606__________________________ References: 1. Jackson, A.R.W. and Jackson, J.M. (2004) Forensic Science. Harlow: Pearson. 2. James, S.H. and Nordby, J.J. (2006) Forensic Science: An Introduction to Scientific and Investigative Techniques (2nd Ed.). Prentice Hall 3. Russell, N.J. Powell, G.M. Jones, J.G. Winterburn, P.J. and Basford J.M. (1982) Blood Biochemistry. Billing &Sons, Worcester. 4. Pepper, I.K. (2005) Crime Scene Investigation., Milton Keynes. Open University Press. 5. Sutton, R. & Trueman, K. (2009) Crime Scene Management – Scene Specific Methods. Wiley. 6. White, P. (ed) (1998) Crime Scene to Court: the essentials of forensic science. London. Royal Society of Chemistry. Page 3 of 3