Additional observations on the nesting behavior of \u3ci\u3eMiscophus (Nitelopterus) californicus\u3c/i\u3e (Ashmead) (Hymenoptera: Crabronidae)

Close-up photographs of nest entry, nest closure and prey transport taken on sandy coastal back dunes in Santa Barbara County, CA by Alice J. Abela substantiate and enhance written descriptions of these nesting be­havior components in Miscophus californicus (Ashmead) [=M. laticeps (Ashmead)] (Hymenoptera: Crabronidae). Dictynidae (Dictyna Sundevall or Emblyna Chamberlin) is introduced as a new host family and host spider leg amputation is revealed for the first time for this small miscophine wasp. Miscophus (Nitelopterus) californicus (Ashmead) (Hymenoptera: Crabronidae) is a small (4.5–7.0 mm) Nearctic miscophine wasp that ranges from California and Arizona north to southern Alberta and Saskatchewan (M. Buck, Royal Alberta Museum, Edmonton, AB, 2020 pers. comm.). This species is extremely common in California with larger black individuals inhabiting relict sand dunes along the Pacific Coast (Wasbauer 1978). The females excavate short shallow burrows in friable soil and hunt various tiny spiders which they immobilize with a sting in the cephalothorax. They transport the prey forward in flight or on the ground, depending on its relative size and weight, and return periodically to an open or closed nest entrance holding the spider face forward and venter to venter. They release the prey on the ground in that position, enter the burrow, pull the spider inside, and, after several spiders are deposited within and oviposition on a single prey occurs, close the burrow and entrance with loose soil. The nesting behavior of Miscophus californicus [as M. laticeps (Ashmead)] was studied in 2010, 2011 and 2012 at Montaña de Oro State Park, San Luis Obispo County, CA by Kurczewski et al. (2012) to clarify variation in previous reports on this species. Voucher specimens from this study were collected from coastal sand dunes in San Luis Obispo and Santa Barbara counties, CA, deposited in the University of California–Davis R.M. Bohart Insect Museum, and identified as M. laticeps by L.S. Kimsey, University of California–Davis. This study was basically in agreement with that on M. californicus by Powell (1967) and in disagreement with the study of M. laticeps by Cazier and Mortenson (1965). Miscophus laticeps is a heretofore previously unpublished synonym of M. californicus in Joanne Slansky Wasbauer’s (1978) Ph. D. Thesis from the University of California–Davis (L.S. Kimsey, University of California–Davis, Davis, CA, 2020 pers. comm.)

New genus Malagiella.

86 p. : ill. (some col.), col. maps ; 26 cm.A new oonopid genus endemic to Madagascar, Malagiella, is proposed and its 10 constituent species newly described and illustrated: M. ambalavo ([male]), M. andringitra ([male, female]), M. fisheri ([m, f]), M. goodmani ([f]), M. nikina ([f]), M. ranavalona ([f]), M. ranomafana ([m, f]), M. toliara ([m, f]), M. valterova ([m, f]), and M. vohiparara ([m, f]). Malagiella is most similar to the Asian genus Camptoscaphiella in both somatic and genitalic features, but differs in some important characters. Unlike Camptoscaphiella, the Malagiella male has a palpal bulb completely fused with the tarsus and a sternum bearing stiff bristles; the female has a round copulatory opening and bifid 4th claws. The species may be recognized by the genitalia. Male palpi are fairly uniform, but differ in segment proportion and details of the embolus complex, which consists of a broad dorsal embolus connected to a laminar ventral prong. Female genitalia are more variable, especially in the curvature of the receptaculum, which spans the range from nearly straight to widely sinuous and occurs in mirror-image versions having opposite coiling. These torsional variants, with females having either left- or right-handed receptacula, probably occur in all species, although they are not evident in species with straight receptacula and (obviously) unknown in species represented by singleton female specimens. Malagiella species are very diverse somatically, ranging from dark, big, and large-eyed species to pale, small, and reduced-eyed ones. Our preliminary clustering uses mostly these somatic features, with some genitalic support, to identify three species groups: ranomafana, vohiparara, and toliara. Other genitalic characters that suggest different groupings are discussed

New genus Molotra

69 p. : ill. (some col.), col. map ; 26 cm.A new oonopid genus endemic to Madagascar, Molotra, is proposed and its six included species are newly described and illustrated: M. molotra, the type species, M. ninae, M. katarinae, M. suzannae, M. tsingy, and M. milloti. Molotra is defined on the basis of its unusual genitalia. The male has the palpal bulb terminating in broad, liplike lobes, unlike any previously described in Oonopidae. The female is equally unusual in lacking an apparent receptaculum, although the genitalia otherwise resemble those of silhouettelloid genera. The species of Molotra form three distinct groups based on somatic and genitalic characters. The M. molotra group includes four large, strongly spined species. The remaining two are morphologically distinct and known only from males. M. tsingy is a small species with unusual palpi that are complex, contorted, and with a resting position along the sternocoxal boundary, instead of an anterior sternal cavity. M. milloti is a very bristly species that differs somatically from other Molotra but has genitalia similar to the M. molotra group. Molotra is known only from Madagascar where the three species groups are strongly disjunct. The M. molotra group occurs in higher elevation forests (1000-1300 m) in northeastern Madagascar, M. tsingy is from low elevation karst (150 m) of the southwest, whereas M. milloti is from a coastal locality in the northwest

The Impact of Glucuronidation on the Bioactivation and DNA Adduction of the Cooked-Food Carcinogen 2-Amino-1-methyl-6-phenylimidazo[4,5-b] pyridine in vivo

UDP-glucuronosyltransferases (UGTs) catalyze the glucuronidation of many different chemicals. Glucuronidation is especially important for detoxifying reactive intermediates from metabolic reactions, which otherwise can be biotransformed into highly reactive cytotoxic or carcinogenic species. Detoxification of certain food-borne carcinogenic heterocyclic amines (HAs) is highly dependent on UGT1A-mediated glucuronidation. 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP), the most mass abundant carcinogenic HA found in well-done cooked meat, is extensively glucuronidated by UGT1A proteins. In humans, CYP1A2 catalyzed N-hydroxylation and subsequent UGT1A-mediated glucuronidation is a dominant pathway in the metabolism of PhIP. Therefore, changes in glucuronidation rates could significantly alter PhIP metabolism. To determine the importance of UGT1A-mediated glucuronidation in the biotransformation of PhIP, UGT1A proficient Wistar and UGT1A deficient Gunn rats were exposed to a single 100 {micro}g/kg oral dose of [{sup 14}C]-PhIP. Urine was collected over 24 h and the PhIP urinary metabolite profiles were compared between the two strains. After the 24 h exposure, livers and colon were removed and analyzed for DNA adduct formation by accelerator mass spectrometry. Wistar rats produced several PhIP and N-hydroxy-PhIP glucuronides that accounted for {approx}25% of the total amount of recovered urinary metabolites. In the Gunn rats, PhIP and N-hydroxy-PhIP glucuronides were reduced by 68-92%, compared to the Wistar rats, and comprised only 4% of the total amount of recovered urinary metabolites. PhIP-DNA adduct analysis from the Gunn rats revealed a correlation between reduced PhIP and N-hydroxy-PhIP glucuronide levels in the urine and increased hepatic DNA adducts, compared to the Wistar rats. These results indicate that UGT1A-mediated glucuronidation of PhIP and N-hydroxy-PhIP is an important pathway for PhIP detoxification. Failure to form glucuronide conjugates results in increases in PhIP bioactivation and DNA adduct formation, which can potentially lead to increases in tumor formation. Therefore, diminished UGT1A activity could pose a significant risk for the development of certain cancers from exposure to PhIP

Determination of the Tissue Distribution and Excretion by Accelerator Mass Spectrometry of the Nonadecapeptide 14C-Moli1901 in Beagle dogs after Intratracheal Instillation

Administration of {sup 14}C-Moli1901 (duramycin, 2622U90), a 19 amino acid polycyclic peptide by intratracheal instillation (approximately 100 {micro}g) into the left cranial lobe of the lung of beagle dogs resulted in retention of 64% of the dose in the left cranial lobe for up to 28 days. In this study, we used accelerator mass spectrometry (AMS) to quantify Moli901 following administration of only 0.045 {micro}Ci of {sup 14}C-Moli901 per dog. Limits of quantitation of AMS were 0.03 (urine) to 0.3 (feces) ng equiv. Moli1901/g. Whole blood and plasma concentrations of {sup 14}C were <5ng/ml at all times after the dose. Concentrations of {sup 14}C in whole blood and plasma declined over the first day after the dose and rose thereafter, with the rise in plasma concentrations lagging behind those in whole blood. During the first 3 days after the dose, plasma accounted for the majority of {sup 14}C in whole blood, but after that time, plasma accounted for only 25-30% of the {sup 14}C in whole blood. Tissue (left and right caudal lung lobe, liver, kidney, spleen, brain) and bile concentrations were low, always less than 0.25% the concentrations found in the left cranial lung lobe. Approximately 13% of the dose was eliminated in urine and feces in 28 days, with fecal elimination accounting for about 10% of the dose. The data presented here are consistent with that obtained in other species. Moli1901 is slowly absorbed and excreted from the lung, and it does not accumulate in other tissues. Moli1901 is currently in the clinic and has proven to be safe in single dose studies in human volunteers and cystic fibrosis patients by the inhalation route. No information on the disposition of the compound in humans is available. This study in dogs demonstrates the feasibility of obtaining that information using {sup 14}C-Moli1901 and AMS

Inflammation and Atrophy Precede Prostate Neoplasia in PhIP Induced Rat Model

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP) has been implicated as a major mutagenic heterocyclic amine in the human diet and is carcinogenic in the rat prostate. In order to validate PhIP induced rat prostate neoplasia as a model of human prostate cancer progression, we sought to study the earliest histologic and morphologic changes in the prostate and to follow the progressive changes over time. We fed 67 male Fischer F344 5 week old rats with PhIP (400 PPM) or control diets for 20 weeks, and then sacrificed animals for histomorphologic examination at age 25 weeks, 45 weeks, and 65 weeks. Animals treated with PhIP showed significantly more inflammation (P=.002 (25wk), >.001(45wk), .016(65wk)) and atrophy (P=.003(25wk), >.001(45wk), .006 (65wk)) in their prostate glands relative to controls. Prostatic intraepithelial neoplasia (PIN) occurred only in PhIP treated rats. PIN lesions arose in areas of glandular atrophy, most often in the ventral prostate. Atypical cells in areas of atrophy show loss of glutathione S-transferase pi immunostaining preceding development of PIN. None of the animals in this study developed invasive carcinomas differing from previous reports. Overall, these findings suggest that the pathogenesis of prostatic neoplasia in the PhIP treated rat prostate proceeds from inflammation to post-inflammatory proliferative atrophy to PIN

New genus Volborattella.

71 pages : illustrations (some color), maps (some color) ; 26 cm. "Species descriptions were generated with the aid of the oonopid PBI descriptive database"--Page 10.A new genus of goblin spider from Madagascar, Volborattella Saucedo and Ubick, is proposed and its five included species newly described and illustrated: V. teresae, the type species, V. guenevera, V. nasario, V. paulyi, and V. toliara. These species differ from other oonopids in several unusual characters, especially the variously modified setae: abdominal scutes having thick recumbent setae with large bases and conspicuous pits; the pedicel region with mats of plumose setae and associated cuticular projections; and anterior metatarsi with prolateral combs. The male palp of Volborattella appears to be unique in having a terminal projection (embolar superior prong, ESP) that forms an abrupt spiral and the female a receptaculum with an accessory duct (curved tube). Volborattella resemble members of the Gamasomorpha complex in lacking leg spines and having a flattened abdomen with complete scutes, but differ genitalically. The Volborattella female has a receptaculum that is wider than long (as opposed to longer than wide in the Gamasomorpha complex) and the male has the embolar region sharply bent (as opposed to evenly curved), which places the genus in the Pelicinus complex. The relationship of Volborattella to other pelicinoids is not resolved. Although the genus most closely resembles some Silhouettella Benoit, Noideattella Álvarez-Padilla et al. and Lionneta Benoit in various genitalic features, somatically it shares with Tolegnaro Álvarez-Padilla et al. and two undescribed Malagasy genera the gamasomorphoid body form and plumose setae. Volborattella females are unusual in having antisymmetrical internal genitalia, with the CTs occurring in either a left or right position, and that these differences in handedness (antisymmetry) are evenly distributed. The shape and size of the CT, as examined through light and scanning microscopy, suggest that it is a coupling pocket for the ESP; if so, Volborattella females are either righties or lefties in their palpal preference

A Novel 14C-Postlabeling Assay Using Accelerator Mass Spectrometry For the Detection of O6-Methyldeoxyguanosine Adducts

Accelerator mass spectrometry (AMS) is currently one of the most sensitive methods available for the trace detection of DNA adducts and is particularly valuable for measuring adducts in humans or animal models. However, the standard approach requires administration of a radiolabeled compound. As an alternative, we have developed a preliminary {sup 14}C-postlabeling assay for detection of the highly mutagenic O{sup 6}-MedG, by AMS. Procedures were developed for derivatizing O{sup 6}-MedG using unlabeled acetic anhydride. Using conventional LC-MS analysis, the limit of detection for the major product, triacetylated O{sup 6}-MedG, was 10 fmoles. On reaction with {sup 14}C-acetic anhydride, using a specially designed enclosed system, the predominant product was {sup 14}C-di-acetyl O{sup 6}-MedG. This change in reaction profile was due to a modification of the reaction procedure, introduced as a necessary safety precaution. The limit of detection for {sup 14}C-diacetyl O{sup 6}-MedG by AMS was determined as 79 attomoles, {approx}18,000 fold lower than that achievable by LSC. Although the assay has so far only been carried out with labeled standards, the degree of sensitivity obtained illustrates the potential of this assay for measuring O{sup 6}-MedG levels in humans

Urinary Metabolites of the Dietary Carcinogen PhIP are Predictive of Colon DNA Adducts After a Low Dose Exposure in Humans

Epidemiologic evidence indicates that exposure to heterocyclic amines (HAs) in the diet is an important risk factor for the development of colon cancer. Well-done cooked meats contain significant levels of HAs which have been shown to cause cancer in laboratory animals. To better understand the mechanisms of HA bioactivation in humans, the most mass abundant HA, 2-amino-l-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP), was used to assess the relationship between PhIP metabolism and DNA adduct formation. Ten human volunteers were administered a dietary relevant dose of [{sup 14}C]PhIP 48-72 h prior to surgery to remove colon tumors. Urine was collected for 24 h after dosing for metabolite analysis, and DNA was extracted from colon tissue and analyzed by accelerator mass spectrometry for DNA adducts. All ten subjects were phenotyped for CYP1A2, NAT2, and SULT1A1 enzyme activity. Twelve PhIP metabolites were detected in the urine samples. The most abundant metabolite in all volunteers was N-hydroxy-PhIP-N{sup 2}-glucuronide. Metabolite levels varied significantly between the volunteers. Interindividual differences in colon DNA adducts levels were observed between each individual. The data showed that individuals with a rapid CYP1A2 phenotype and high levels of urinary N-hydroxy-PhIP-N{sup 2}-glucuronide, had the lowest level of colon PhIP-DNA adducts. This suggests that glucuronidation plays a significant role in detoxifying N-hydroxy-PhIP. The levels of urinary N-hydroxy-PhIP-N{sup 2}-glucuronide were negatively correlated to colon DNA adduct levels. Although it is difficult to make definite conclusions from a small data set, the results from this pilot study have encouraged further investigations using a much larger study group