Light-induced enzyme system leading to pigmentation.

Alpha-Chymotrypsin was light sensitized by acylating with cis-cinnamoyl ester, a substrate interconvertible to the trans form by ultraviolet (UV) light. The degree of acylation by this method was complete leaving no residual activity of the enzyme. Upon UV irradiation the inhibited enzyme regained about 70% of its original activity, thereby adding light-sensitiveness to the proteolytic enzyme. In seeking a photographic application of the light-sensitized enzyme, a pigmenting enzyme was incorporated with it. The coupled enzyme system was shown to exhibit a light signal in the form of dark pigment slurry.     

Laser-Stimulated Fluorescence in Paleontology

Fluorescence using ultraviolet (UV) light has seen increased use as a tool in paleontology over the last decade. Laser-stimulated fluorescence (LSF) is a next generation technique that is emerging as a way to fluoresce paleontological specimens that remain dark under typical UV. A laser’s ability to concentrate very high flux rates both at the macroscopic and microscopic levels results in specimens fluorescing in ways a standard UV bulb cannot induce. Presented here are five paleontological case histories that illustrate the technique across a broad range of specimens and scales. Novel uses such as back-lighting opaque specimens to reveal detail and detection of specimens completely obscured by matrix are highlighted in these examples. The recent cost reductions in medium-power short wavelength lasers and use of standard photographic filters has now made this technique widely accessible to researchers. This technology has the potential to automate multiple aspects of paleontology, including preparation and sorting of microfossils. This represents a highly cost-effective way to address paleontology''s preparatory bottleneck.     

Technical note: Ultraviolet reflectance-absorbance photography; An easy,inexpensive research tool

Photography in the ultraviolet wavelength is possible by use of special lenses, special filters, or both. This paper makes available pertinent information on an easy, inexpensive UV photographic technique. A comprehensive bibliography is provided. By using a flash guide number, lens apertures for various lens-subject distances can be calculated. The inexpensive technique is accomplished by simple adaptation of a Kodak Wratten 18A filter to the normal camera lens. The method is equally suited for living material, dried herbarium material, and chromatograms. The technique is useful in studies of pollination ecology, insect energetics, taxonomy, and flavonoid chemistry.     

Inhibition or initiation of a radical polymerization reaction by an ultraviolet-induced enzymatic process

alpha-Chymotrypsin was modified to a light-controllable enzyme derivative by acylating active serine 195 residue with a cinnamoyl group or analogue. Upon UV irradiation the acylgroup could be isomerized, leading to release of the inhibiting group. Enzymatic activity could thus be regulated by means of UV light. A full 100% inhibition of the enzymatic activity could not be reached by the cinnamoyl derivative. Only posttreatment with diisopropylfluorophosphate yields a fully inactive enzyme derivative. The shelf-life of the inhibited enzyme was rather poor. Only freeze-dried samples could be used for several months without significant recovery of activity. Adapting the sensitivity of the system to visible light seems limited to the size of an enzyme's active site. Combination of the enzymatic system producing an inhibitor or an initiator with a polymerization reaction can result in a photographic process with a higher amplification factor.     

MEASUREMENT OF PHOTOGRAPHIC QUALITY AND INDIVIDUAL DISTINCTIVENESS FOR THE PHOTOGRAPHIC IDENTIFICATION OF HUMPBACK WHALES, MEGAPTERA NOVAEANGLIAE

Accurate identification of humpback whales from photographic identification data depends on the quality of the photographs and the distinctiveness of the flukes. Criteria for evaluating photographic quality and individual distinctiveness were developed involving judgments about overall quality or distinctiveness and about specific aspects of each. These criteria were tested for the level of agreement among judges. The distinctiveness scheme was tested for the independence of distinctiveness judgments and photographic quality. Our results show that judges could agree when evaluating specific and overall aspects of photographic quality and individual distinctiveness. The level of agreement varied for different pairs of judges, and less adept judges were identified. Ability to agree on evaluations of photographic quality was independent of the experience of the judges. Overall photographic quality and overall distinctiveness were successfully predicted from more specific variables, but the agreement between judges for these was not significantly greater than the agreement for the overall measures judged directly. There was no correlation between individual distinctiveness and photographic quality for four of the five judges, but the power of this rest may be low. Analyses of photographic identification data frequently require evaluations of photographic quality and individual distinctiveness. To obtain reliable results from such analyses, evaluation schemes and judges should be tested to ensure reliable and consistent evaluations.     

Simple Technique for Dark-Field Photography of Immunodiffusion Bands

A simple dark-field photographic technique was developed which enables laboratory personnel with minimal photographic training to easily record antigen-antibody patterns on immunodiffusion plates.     

Assessing the capabilities of a 4kx4k CCD camera for electron cryo-microscopy at 300kV

CCD cameras have numerous advantages over photographic film for detecting electrons; however the point spread function of these cameras has not been sufficient for single particle data collection to subnanometer resolution with 300kV microscopes. We have adopted spectral signal to noise ratio (SNR) as a parameter for assessing detector quality for single particle imaging. The robustness of this parameter is confirmed under a variety of experimental conditions. Using this parameter, we demonstrate that the SNR of images of either amorphous carbon film or ice embedded virus particles collected on a new commercially available 4kx4k CCD camera are slightly better than photographic film at low spatial frequency (<1/5 Nyquist frequency), and as good as photographic film out to half of the Nyquist frequency. In addition it is slightly easier to visualize ice embedded particles on this CCD camera than on photographic film. Based on this analysis it is realistic to collect images containing subnanometer resolution data (6-9A) using this CCD camera at an effective magnification of approximately 112000x on a 300kV electron microscope.     

Imagining the Real: The Photographic Image and Imagination in Knowledge Production

The exploratory discussion in this article starts from the fact that it is the realism of photographic representations which enables them, in an indexical sense, to point back to a reality beyond themselves as images. In the same vein, it is as a metonymic space-time fragment that the photograph can indicate a continuation of reality beyond its own framing of the visible. Or, putting it differently, rather than constituting transparent representations, presence in photographs is evoked through absence of the real. What is not problematized in photographic theory and visual anthropology is that photographs thus depend on imagination for their interpretative connection to reality. My argument sees photographic practice as interference, which pushes the medium past the implicit positivist premise for visual knowledge production in anthropology. Furthermore, when understanding the ability to imagine as movements in reason, the separation between imagination and reason, presumed necessary for the scientific production of knowledge, is also challenged. Concerned with rethinking photography in visual anthropology, imagination’s role in knowledge production will be explored through my photographic art project, Houses/Homes.     

Portrait Obsession: Reproducing Gypsy Identity through Photographs

This article examines the importance Gypsies attribute to photographic images of themselves, suggesting that such images play a crucial role in the reproduction and questioning of their identity. Based on empirical evidence collected among Gypsy communities in the Lisbon urban area, the article tests its main hypothesis through a detailed analysis of two key dimensions: the photographic session as an intense interactive situation and the content of the photographic images. An analytical reflection concludes that the Gypsy photography phenomenon might be understood as a kind of ritual.     

Histological Processing in Autoradiography: Loss of Radioactivity

Histological methods suitable for use in autoradiographic technics are described. An investigation has been carried out on the amount of activity lost from rat and human tissues during fixation and dehydration. Losses in the processing fluids varied from 25% to 90% of the initial activity for radioactive phosphorus and 4% to 20% for radioactive iodine in various fixatives.

The care necessary in handling sections if distribution of total activity is being studied is emphasized and floating on absolute alcohol is suggested as an alternative to warm mercury. Various procedures for staining sections before application of photographic emulsion and after developing are discussed. Ehrlich's hematoxylin applied regressively has given good results and eosin has been used successfully as a counterstain. Orth's lithium carmine is resistant to photographic developer and also Feulgen's stain counterstained with fast green can be used before covering the slides with photographic emulsion.     

Photography as a tool of research and documentation in plant tissue culture

Summary Scientific photography is an important facet of plant tissue culture. The aim of photography in plant tissue culture should be to illustrate clearly the developmental stages occurring in vitro. However, the photographic results presented in publications are often poor, and morphogenetic responses are often not clearly documented. Plant tissue culture is a very visual science, and the valuable tool of photography is often not used properly. If the morphogenetic responses are not well documented, an important part of the reserch is missed, and the report ends up having limited scientific value. Simple methods for improving the results of photography in plant tissue culture are discussed, along with photographic equipment, photomacrography, stereophotomicrography, suitable backgrounds for photography, use of a digital scanner, and the construction of photographic plates.     

ESTIMATION OF BODY MASS IN THE SOUTHERN ELEPHANT SEAL, MIROUNGA LEONINA, BY PHOTOGRAMMETRY AND MORPHOMETRICS

A simple photographic technique was developed to indirectly estimate body mass data for southern elephant seal ( Mirounga leonina ) cows (postlactation), yearlings, and immature males and females. Regressions of mass on both photographic and morphometric variables (together and separately) yielded useful, predictable models. Using such variables, the best estimation of the actual mass was for postlactation cows, with a 95% confidence interval of ± 2.66% of the predicted body mass. Although combining photographic and morphometric variables produced the most reliable models specifically for cows and yearlings, the most practical model contained only the morphometric variables length and girth squared. Side area was the best correlated single photographic variable and this corresponded with other studies. Photogrammetry could be useful when animals cannot be sedated and are located on a flat surface, but it does require animals to be motionless when approached. Thus, the procedure may be more suited to bulls rather than other age classes and could have a role in studies where large numbers of mass estimations are rapidly required. If sedation is utilized in smaller animals, then the use of body length and girth is the most suitable indirect mass estimation technique to avoid the use of heavy weighing equipment.     

Photographic colorimetry as a quantitative cytochemical method

Summary A method for quantitative cytophotometry based on the photographic method of Ornstein is described. Taking special precautions, photographic negatives are made of microscopic objects with light from the appropriate part of the spectrum. Enlarged prints, developed in a blue colour, are made from these negatives. Stirring with a stream of nitrogen was applied in this procedure.The images of the objects in the blue print are cut out, and the amount of dye proportional to the integrated extinction of the objects is measured in a colorimeter. This method, for which the name photographic colorimetry is proposed, was tested on Feulgen-stained nuclei from various sources. The reproducibility of the method was found to range from 3 to 5%.Submitted in partial fulfillment of the requirements for Ph. D. degree (Den Tonkelaar 1963).     

Photographic detection of fluorescent-labelled oligodeoxynucleotide in the blotting format by peroxyoxalate chemiluminescence

The preparation of a fluorescent labelled oligonucleotide and its photographic detection by peroxyoxalate chemiluminescence (PO-CL) are described. Fluorescent labelling of an oligonucleotide (15-mer) was performed with naphthalene-2,3-dicarboxaldehyde to give an N-substituted 1-cyanobenz[f]isoindole (CBI) derivative (CBI-15-mer). For the photographic detection of CBI-15-mer, the bis(2,6-difluorophenyl) oxalate (DFPO)-dimethyl phthalate (DMP) system was selected to obtain a long-lived CL emission. After optimizing the conditions for the CL reaction, the system was applied to the photographic detection, and as little as 250 fmol per spot of CBI-15-mer on a membrane were detected as a visible spot with an instant photographic film. © 1998 John Wiley & Sons, Ltd.     

A key for the identification of the hair of mammals of a snow leopard (Panthera uncia) habitat in Nepal

Analysis of prey remains in scats, particularly hairs, is widely used to study diet of mammalian predators, but identification of hair is often difficult because hair structures vary considerably both within and between species. Use of photographic reference of diagnostically important hair structures from mammals occurring in a predator's habitat has been found to he convenient for routine identification. A photographic reference key was developed for the identification of hairs of the mammals known to occur in a snow leopard ( Panthera uncia ) habit at in the Annapurna Conservation Area, Nepal. The key included a photographic reference of the diagnostic hair structures of nine species of wild and five species of domestic mammals. The cross-sectional appearance, shape and arrangement of medulla, the ratio of cortex to medulla. and the form and distribution of pigment in medulla and cortex were important diagnostic aids in the identification of hairs.     

A Basic Camera Unit for Medical Photography

A camera unit suitable for most medical photographic purposes is described. The unit comprises a single-lens reflex camera, an electronic flash unit and supplementary lenses. Simple instructions for use of th''s basic unit are presented. The unit is entirely suitable for taking fine-quality photographs of most medical subjects by persons who have had little photographic training.     

Conventional digital cameras as a tool for assessing leaf area index and biomass for cereal breeding

Affordable and easy-to-use methods for assessing biomass and leaf area index （LAI） would be of interest in most breeding programs. Here, we describe the evaluation of a protocol for photographic sampling and image analysis aimed at providing low-labor yet robust indicators of biomass and LAI. In this trial, two genotypes of triticale, two of bread wheat, and four of tritordeum were studied. At six dates during the growing cycle, biomass and LAI were measured destructively, and digital photography was taken on the same dates. Several vegetation indices were calculated from each image. The results showed that repeatable and consistent values of the indices were obtained in consecutive photographic samplings on the same plots. The photographic indices were highly correlated with the destructive measure-ments, though the magnitude of the correlation was lower after anthesis. This work shows that photographic assess-ment of biomass and LAI can be fast, affordable, have good repeatability, and can be used under bright and overcast skies. A practical vegetation index derived from pictures is the fraction of green pixels over the total pixels of the image, and as it shows good correlations with all biomass variables, is the most robust to lighting conditions and has easy interpretation.     

Fungal biosorption of silver particles on 20th-century photographic documents

Microbial deterioration is a common problem in photographic collections and is considered a major cause of loss of documents. However, few studies so far have been addressed to biological damage on these materials. Several species of naturally occurring fungi can cause infections on the gelatin-silver emulsion of both positive and negative photographic material, producing defacement and loss of mechanical and aesthetical properties of the objects. In this study a particular phenomenon, spontaneously caused by fungi on 20th-century photographic films and positive supports, was documented by means of variable pressure scanning electron microscopy (VP-SEM) combined with electronic dispersion spectroscopy (EDS). This technique allowed the observation of entire, unaltered films without metallisation thus with a not invasive approach. The ability of some fungi to alter the distribution of silver crystals in the gelatin emulsion was described thanks to a backscattered electrons detector that showed differences in the atomic number of the visualised objects, giving rise to an appreciable contrast in case of different chemical composition.     

Aminomethyl coumarin acetic acid: A new fluorescent labelling agent for proteins

Summary A new fluorescent protein labelling agent, 7-amino-4-methyl coumarin-3-acetic acid (AMCA), emits in the blue region (440–460 nm) on activation with UV light (350 nm). The active reagent is theN-hydroxysuccinimide ester which reacts with lysine residues under mild conditions to form photostable amide links.The Stokes shift of 100 nm compared to 30 nm for Fluorescein isothiocyanate (FITC) allows easy filter discrimination of exciting and emitting radiation. The agent has been demonstrated in use for fluorohistochemical examination of human kidney glomeruli, using the sandwich technique and compared with the same procedure using FITC-labelled antibodies. The good quantum yield coupled with convenient emission lines in the mercury spectrum allows photographic exposure time of fluorescent labelled sections to be reduced to a quarter of that required for a corresponding FITC conjugate.AMCA—immunoglobulin conjugates were not susceptible to photobleaching and have a storage life at – 20° C of more than two years.To whom correspondence and reprint requests should be addressed.     

The quantitation of fluorescence by photography.

A method based on theory has been developed for the photographic quantitation of fluorescent substances. DNA stained with ethidium in agarose gels is used as an example of an application of this method. In the course of developing this method we have demonstrated that the empirical methods employed by others authors can give rise to large systematic errors. We have also developed an approximate method based on photographic theory, avoiding the use of digital integration which is required by the rigorous method.