Injuries caused by gunshots can produce what bloodstain pattern analysts know as "backspatter." Observations about the presence or absence of backspatter on an individual may be used in court as evidence of guilt or innocence. The discharge of three firearms (.22 caliber revolver, .38 caliber revolver, and .308 caliber rifle) and the resulting impact of bullets on a blood source were recorded using high-speed digital video imaging. Blood droplets, firearm muzzle gases, and ballistic shock waves were visualized using standard reflected light and shadowgraphy imaging techniques. A significant interaction between air currents, muzzle gases, and particulate material emanating from the firearms upon discharge with backspattered blood was observed. Blood droplets, initially spattered back toward the firearm and the shooter, were observed to change direction under the influence of firearm-induced air currents and were blown forward toward and beyond their original source location. Implications for experts testifying in court and for bloodstain pattern instructors are discussed.

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This study was designed to produce the first baseline measure of the reliability of bloodstain pattern classifications on fabric surfaces. Experienced bloodstain pattern analysts classified bloodstain patterns on pairs of trousers that represented three fabric substrates. Patterns also varied in type (impact, cast-off, expiration, satellite stains from dripped blood, and transfer) and extent. In addition, case summaries that accompanied each pattern contained contextual cues that either supported the correct answer (i.e., positive bias), were misleading toward an incorrect answer (i.e., negative bias), or contained no directional information (i.e., neutral). Overall, 23% percent of the resulting classifications were erroneous. The majority (51%) of errors resulted from analysts misclassifying satellite stains from dripped blood. Relative to the neutral information, the positive-bias information increased correct classifications and decreased erroneous classifications, and the negative-bias information decreased correct classifications and increased erroneous classifications. The implications of these findings for BPA are discussed.

This study describes a method for establishing match criteria used in forensic DNA typing. The validity of applying different match criteria based upon the molecular weight of a DNA band is discussed. The match criteria presented allow visually matching DNA patterns to be confirmed by computer assisted image analysis over the entire range of the sizing ladder. Approximately 5000 intragel and 5000 intergel comparisons were made between the restriction fragment length polymorphism (RFLP) DNA band sizes obtained from casework, mock cases, and environmentally insulted samples and the band sizes obtained from their corresponding bloodstain standards (controls). Analyses of these data suggested that fragments located in different molecular weight size regions of an analytical gel required different match criteria for assessing a visual match. The results of these analyses support the use of the following match criteria: Intragel 0.5–10 kb = ±1.7%, 10–15 kb = ±3.2%, 15–22.6 kb = ±5.8%; Intergel and blind control 0.5–10kb = ±3.0%, 10–15 kb = ±4.2%, 15–22.6 kb = ±10.0%; and human cell-line K562 and the monomorphic locus D7Z2 = ±2.5%. Each match criterion was also evaluated with respect to the distance in millimeters between matching bands throughout the 0.5–22.6 kb molecular weight size range. Applying these match criteria to different gel regions has been shown to be valid and reliable in comparisons conducted on more than 10,000 validation samples, in over 500 forensic cases and in more than 200 searches of a criminal sexual offender (CSO) database containing over 5000 individuals.

Vaginally inserted plastic tampon applicators were obtained from 42 female volunteers. The applicators were examined for the presence of ABH blood group substances, phosphoglucomutase (PGM), amylase, acid phosphatase, P30, and intact spermatozoa. Each applicator was accompanied by a control blood sample, a saliva specimen, a brief sexual and menstrual history, and method of birth control of the donor. Eight of the male sexual partners of the donors submitted blood and saliva samples. One male sexual partner submitted only a saliva sample. ABH blood group substances corresponding to the donor were recovered from 36 of the 42 applicators. The remaining 6 applicators revealed a combination of the donor's and sexual partner's ABH substances. The female's PGM type was recovered from 34 of the applicators. The remaining 8 applicators failed to show PGM activity. Of the applicators, 15 indicated evidence of prior sexual intercourse by the detection of ABH substances not consistent with the applicator donor (6 samples), high levels of acid phosphatase (11 samples), or recovery of spermatozoa (8 samples) or some combination of these. All applicator samples failed to show the presence of either P30 activity or PGM factors foreign to the female.

This study originated from discussions and recommendations of the Technical Working Group on DNA Analysis Methods (TWGDAM). Four bloodstain deoxyribonucleic acid (DNA) extraction protocols and five semen stain DNA extraction protocols were evaluated. Nine laboratories participated in the extraction of DNA from 20 bloodstains and 20 semen stains using each protocol. All blood and semen stains originated from a single donor and were prepared under uniform conditions to permit the direct comparison of DNA yields and restriction fragment lengths. The extracted DNA from approximately 600 bloodstains and 700 semen stains was quantified by yield gel analysis and a slot blot hybridization technique. The extracted DNA was digested and restriction fragment length polymorphism (RFLP) patterns were generated using three single-locus probes. The RFLP sizing data produced from the blood and semen stains were evaluated with respect to (1) DNA extraction method, (2) gel length, (3) agarose type, (4) presence or absence of ethidium bromide in the gel, and (5) fragment sizes obtained from DNA isolated directly from the donor's liquid blood. This study demonstrates conclusively that high-molecular-weight DNA can be isolated using either organic or nonorganic DNA extraction protocols and that the resulting RFLP sizes are highly reproducible regardless of gel length, agarose type, or presence/absence of ethidium bromide.

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