Study of the Anatomy of the Alimentary Canal of Brochymena quadripustulata (Hemiptera:Pentatomidae)

An anatomical study of the alimentary canal and associated salivary apparatus was conducted for the pentatomid, Brochymena quadripustulata. The esophagus, ventriculus, pylorus, rectum, principal salivary glands and ducts are described and illustrated. Described structures of Brochymena quadripustulata are compared with various species of pentatomids and other hemipterans

Composition-tuned smeared phase transitions

Phase transitions in random systems are smeared if individual spatial regions can order independently of the bulk system. In this paper, we study such smeared phase transitions (both classical and quantum) in substitutional alloys A$_{1-x}$B$_x$ that can be tuned from an ordered phase at composition $x=0$ to a disordered phase at $x=1$. We show that the ordered phase develops a pronounced tail that extends over all compositions $x<1$. Using optimal fluctuation theory, we derive the composition dependence of the order parameter and other quantities in the tail of the smeared phase transition. We also compare our results to computer simulations of a toy model, and we discuss experiments.Comment: 6 pages, 4 eps figures included, final version as publishe

Effects of rarefaction on cavity flow in the slip regime

The Navier-Stokes-Fourier equations, with boundary conditions that account for the effects of velocity-slip and temperature-jump, are compared to the direct simulation Monte Carlo method for the case of a lid-driven micro-cavity. Results are presented for Knudsen numbers within the slip-flow regime where the onset of nonequilibrium effects are usually observed. Good agreement is found in predicting the general features of the velocity field and the recirculating flow. However, although the steady-state pressure distributions along the walls of the driven cavity are generally in good agreement with the Monte Carlo data, there is some indication that the results are starting to show noticeable differences, particularly at the separation and reattachment points. The modified Navier-Stokes-Fourier equations consistently overpredict the maximum and minimum pressure values throughout the slip regime. This highlights the need for alternative boundary formulations or modeling techniques that can provide accurate and computationally economic solutions over a wider range of Knudsen numbers

Micro-scale cavities in the slip - and transition - flow regimes

Differences between Navier-Stokes-Fourier (NSF) slip/jump solutions and direct simulation Monte-Carlo (DSMC) computations are highlighted for a micro lid-driven cavity problem. The results indicate a need for better modelling techniques which at the same time retain low computational cost of NSF models. We also highlight the fact thatmany micro-flows that have been considered are simple planar flows and typical classification systems are defined on such flows. We show that for complex flows, such as thedriven cavity, non-equilibrium effects are more appreciable and their onset occurs at lower Knudsen numbers than expected

Evaluation of a Formula that Categorizes Female Gray Wolf Breeding Status by Nipple Size

The proportion by age class of wild Canis lupus (Gray Wolf) females that reproduce in any given year remains unclear; thus, we evaluated the applicability to our long-term (1972–2013) data set of the Mech et al. (1993) formula that categorizes female Gray Wolf breeding status by nipple size and time of year. We used the formula to classify Gray Wolves from 68 capture events into 4 categories (yearling, adult non-breeder, former breeder, current breeder). To address issues with small sample size and variance, we created an ambiguity index to allow some Gray Wolves to be classed into 2 categories. We classified 20 nipple measurements ambiguously: 16 current or former breeder, 3 former or adult non-breeder, and 1 yearling or adult non-breeder. The formula unambiguously classified 48 (71%) of the nipple measurements; based on supplemental field evidence, at least 5 (10%) of these were incorrect. When used in conjunction with an ambiguity index we developed and with corrections made for classifications involving very large nipples, and supplemented with available field evidence, the Mech et al. (1993) formula provided reasonably reliable classification of breeding status in wild female Gray Wolves

Gray Wolf (\u3ci\u3eCanis lupus\u3c/i\u3e) Dyad Monthly Association Rates by Demographic Group

Preliminary data from GPS-collared wolves (Canis lupus) in the Superior National Forest of northeastern Minnesota indicated wolves had low association rates with packmates during summer. However, aerial-telemetry locations of very high frequency (VHF)-radioed wolves in this same area showed high associations among packmates during winter. We analyzed aerial-telemetry-location data from VHF-collared wolves in several packs (n=18 dyads) in this same area from 1994-2012 by month, and found lowest association rates occurred during June. While other studies have found low association among wolf packmates during summer, information on differences in association patterns depending on the wolf associates’ demographics is sparse. During May-July, association rates were greatest for breeding pairs, followed by sibling dyads, and lowest for parent–offspring dyads. Our findings improve our understanding of how individual wolf relationships affect monthly association rates. We highlight some important remaining questions regarding wolf packmate associations

Yellowstone wolf (\u3ci\u3eCanis lupus\u3c/i\u3e) density predicted by elk (\u3ci\u3eCervus elaphus\u3c/i\u3e) biomass

The Northern Range (NR) of Yellowstone National Park (YNP) hosts a higher prey biomass density in the form of elk (Cervus elaphus L., 1758) than any other system of gray wolves (Canis lupus L., 1758) and prey reported. Therefore, it is important to determine whether that wolf–prey system fits a long-standing model relating wolf density to prey biomass. Using data from 2005 to 2012 after elk population fluctuations dampened 10 years subsequent to wolf reintroduction, we found that NR prey biomass predicted wolf density. This finding and the trajectory of the regression extend the validity of the model to prey densities 19% higher than previous data and suggest that the model would apply to wolf–prey systems of even higher prey biomass. Le domaine nord (Northern Range; NR) du parc national de Yellowstone (YNP) contient une biomasse de proies de plus grande densité, représentée par les wapitis (Cervus elaphus L., 1758), que tout autre système de loups gris (Canis lupus L., 1758) et proies connu. Il importe donc de déterminer si le système loups–proies concorde avec un modèle établi de longue date qui relie la densité des loups a` la biomasse des proies. En nous servant de données de 2005 a` 2012 après l’atténuation sur une période de 10 ans des fluctuations de la population de wapitis a` la suite de la réintroduction des loups, nous avons constaté que la biomasse des proies du NR prédisait la densité des loups. Cette constatation et la trajectoire de la régression élargissent la validité du modèle a` des densités de proies de 19 % supérieures aux données antérieures et donnent a` penser que le modèle s’appliquerait a` des systèmes loups–proies de biomasse de proies encore plus grande

White-tailed Deer (\u3ci\u3eOdocoileus virginianus\u3c/i\u3e) Subsidize Gray Wolves (\u3ci\u3eCanis lupus\u3c/i\u3e) During a Moose (\u3ci\u3eAlces americanus\u3c/i\u3e) Decline: A Case of Apparent Competition?

Moose (Alces americanus) in northeastern Minnesota have declined by 55% since 2006. Although the cause is unresolved, some studies have suggested that Gray Wolves (Canis lupus) contributed to the decline. After the Moose decline, wolves could either decline or switch prey. To determine which occurred in our study area, we compared winter wolf counts and summer diet before and after the Moose decline. While wolf numbers in our study area nearly doubled from 23 in winter 2002 to an average of 41 during winters 2011–2013, calf:cow ratios (the number of calves per cow observed during winter surveys) in the wider Moose range more than halved from 0.93 in 2002 to an average of 0.31 during 2011–2013. Compared to summer 2002, wolves in summers 2011–2013 consumed fewer Moose and more White-tailed Deer (Odocoileus virginianus). While deer densities were similar during each period, average vulnerability, as reflected by winter severity, was greater during 2011–2013 than 2002, probably explaining the wolf increase. During the wolf increase Moose calves remained a summer food item. These findings suggest that in part of the Moose range, deer subsidized wolf numbers while wolves also preyed on Moose calves. This contributed to a Moose decline and is a possible case of apparent competition and inverse-density-dependent predation