The presence of occipital hair in the pilonidal sinus cavity-a triple approach to proof.

PURPOSE: Hair in the pilonidal sinus is not growing within the sinus cavity, as hair follicles are not present there. Not few pilonidal patients do not have intergluteal hair, which is said to be the causative agent of folliculitis and pilonidal genesis. So, what is the real source of the hair forming the typical pilonidal hair nest? METHODS: A trifold approach was used: First, axial hair strength testing of pilonidal hair and body hair harvested from head, lower back (glabella sacralis), and cranial third of intergluteal fold. Hair strength match was compared clinically. Second, comparative morphological examination by expert forensic biologist of hair from sinus and dorsal body hair. Third, statistical Bayesian classification of every single sinus hair based on its strength was done to determine the most probable region of origin. RESULTS: Using clinical hair strength comparison, in 13/20 patients, head hair is the stiffest hair, followed by intergluteal hair. Only in 6/20 patients, this is the case with hair from the glabella sacralis. According to comparative morphological comparison, a minimum of 5 of 13 hair nests with possible hair allocation examined contain hair from the occiput. In 5/18 nests, hair could not be determined to a specific location though. Statistical classification with correction for multiple testing shows that 2 nests have hair samples that are at least 100 times more probable to originate from head or lower back than from intergluteal fold. CONCLUSION: We saw our null hypothesis that "hair in the sinus cavity is from the intergluteal region" rejected by each of three different approaches. There is strong evidence that occipital hair is present regularly in pilonidal sinus nests. We should start thinking of occipital hair as an important hair source for the development of the pilonidal hair nest.

The nocturnal oviposition behaviour of blowflies (Diptera: Calliphoridae) in Central Europe and its forensic implications.

Numerous factors may cause delayed colonisation of a corpse by blowflies, leading to a discrepancy between the entomologically determined post-mortem interval (PMI) and the time of death. Blowflies, for example, are considered to be inactive at night, however, published observations are contradictory. In the present study, several field experiments and one type of indoor experiment were conducted in summer of 2004 and 2005 in order to investigate the nocturnal ovipositional behaviour of blowflies. In the field, two types of bait, dead hedgehogs and fresh beef liver, were placed at night in different urban and rural locations in Frankfurt and in Munich, Germany. For the indoor-experiments beef liver was placed in small plastic boxes containing caged Lucilia sericata females in the evening and left overnight. At night, no ovipositon was observed in the field (n=51, T=10-24 degrees C). Nocturnal oviposition in complete darkness occurred in the plastic boxes in two of six cases (T=25 degrees C). Considering the behavioural and physiological characteristics of flies we suggest that nocturnal oviposition of blowflies appears to be unlikely under natural conditions in Central Europe but may occur under certain circumstances, such as unusual high nightly temperatures and the presence of gravid flies with an appropriate arousal threshold.

The retina of five atherinomorph teleosts: photoreceptors, patterns and spectral sensitivities.

We investigated the spectral and morphological features of the photoreceptors of five atherinomorph teleosts, representing two different orders, and with different life styles and habitats, the Beloniformes and Atheriniformes. The retinae of Belone belone (Belonidae), Dermogenys pusillus (Hemiramphidae), Atherina boyeri (Atherinidae), Marosatherina ladigesi (Telmatherinidae), and Melanotaenia maccullochi (Melanotaeniidae) were examined by light and electron microscopy and microspectrophotometry. In addition to rods, five morphologically different cone types were identified: short, intermediary and long single cones, and double cones which are arranged in distinct specific mosaics. Sporadically, triple cones were also found. Double cones were longer-wave-sensitive, but no general correlation between single cone morphology and spectral sensitivity could be demonstrated. The rods had lambda(max) close to 506-509 nm. The lambda(max) of cone visual pigments ranged from about 368 nm to 578 nm. Ultraviolet-sensitive single cones were present in the three freshwater species, M. ladigesi, M. maccullochi and D. pusillus and three spectrally distinct short-wave-sensitive single cone classes were identified in M. maccullochi. In M. ladigesi, spectral sensitivity varied among individuals due to varying rhodopsin/porphyropsin mixtures. In D. pusillus and M. maccullochi polymorphism of the longer-wave cone pigments might occur. These findings are discussed with respect to phylogeny, photic habitat, behavior and feeding habits.