The Development and Evolution of the Turtle Body Plan: Inferring Intrinsic Aspects of the Evolutionary Process from Experimental Embryology

The body plan of turtles is unique among tetrapods in the presenceof the shell. The structure of the carapace involves a uniquerelationship between the axial and the appendicular skeletons.A common developmental mechanism, an epithelial-mesenchymalinteraction, has been identified in the early stages of carapacedevelopment by means of basic histological and immunofluorescencetechniques. By analogy to other structures initiated by epithelial-mesenchymalinteractions, it is hypothesized that carapace development isdependent on this interaction in the body wall. Surgical perturbationswere designed to test the causal connection between the epithelial-mesenchymalinteraction in the body wall and the unusual placement of theribs in turtles. By comparison to data available on body wallformation in avian embryos, these experiments also shed lighton the segregation of somitic and lateral plate cell populationsand the embryonic origin of the scapula in turtles. This study specifically addresses the ontogeny of a unique tetrapodbody plan. The ontogenetic information can be used to make inferencesabout the phytogeny of this body plan and how it could haveevolved from the more typical primitive tetrapod. On a moregeneral level this studyexplores the potential role of commondevelopmental mechanisms in the generation of evolutionary novelties,and the developmental incongruities between homologous skeletalelements in different groups of tetrapods.     

Evaluation of Attractants to Improve Trapping Success of Nutria on Louisiana Coastal Marsh

ABSTRACT Nutria (Myocastor coypus) are an important part of the Louisiana (USA) fur industry, but high densities of nutria cause extensive damage to coastal marsh ecosystems. Hence, there is a need to develop improved methods for targeted management of nutria. We screened 14 olfactory cues as potential lures for nutria, first in controlled settings and then in the field, to see if nutria capture rates using foothold traps would increase. In Y-maze trials, nutria most frequently selected olfactory cues of a synthetic formulation of nutria anal-gland secretion and nutria fur extract. We examined the 3 most selected attractants in Y-maze trials and female nutria urine under field conditions to compare trapping success over untreated traps. Capture probability was nearly 2.5 times greater for fur wash than control and 2 times greater for urine than control (relative risk = 2.43 and 2.01, respectively). The results suggest that use of semiochemicals and synthetic formulations of semiochemicals increased nutria trapping success. Development and use of effective synthetic semiochemicals could benefit resource managers nationwide who are responsible for reducing damage caused by this invasive herbivore.     

Using DNA Barcodes to Identify Bird Species Involved in Birdstrikes

Abstract: We determined effectiveness of using mitochondrial DNA barcodes (cytochrome c oxidase subunit 1 [CO1]) to identify bird-aircraft collision (birdstrike) cases that lacked sufficient feather evidence for morphological diagnosis. From September through December 2006, 821 samples from birdstrike events occurring in the United States were submitted for DNA analysis. We successfully amplified a CO1 DNA barcode product from 554 (67.5%) of the samples; 267 (32.5%) did not contain viable DNA and depended on morphological methods (microscopy) for Order or Family level identification. We deemed 19 cases inconclusive either because the DNA barcode recovered from the sample did not meet our 98% match criteria when compared to the Barcode of Life Database (BoLD) or because the DNA barcode matched to a set of ≥ 2 closely related species with overlapping barcodes, preventing complete species identification. Age of the sample (≤6 months) did not affect DNA viability, but initial condition of the sample and the collection method was critical to DNA identification success. The DNA barcoding approach has great potential in aiding in identification of birds (and wildlife) for airfield management practices, particularly in regions of the world that lack the vast research collections and individual expertise for morphologic identifications.     

Y chromosome microsatellite markers identified from the tammar wallaby (Macropus eugenii) and their amplification in three other macropod species

Microsatellites were identified from three fully sequenced Y chromosome‐specific bacterial artificial chromosome clones from the tammar wallaby, Macropus eugenii. Ten microsatellites were genotyped in male tammar wallabies. Four loci were polymorphic with between two and six alleles per locus. Eleven different haplotypes were identified from 22 male tammar wallabies. No amplifications were obtained from female samples. Each microsatellite was also shown to amplify reliably in at least one other macropod species. These markers may therefore prove useful as some of the first male‐specific genetic markers for marsupials, with potential application to studies of male‐biased dispersal and mating systems.     

Microsatellite loci from the Caribbean Fruit Fly,Anastrepha suspensa (Diptera: Tephritidae)

The lack of polymorphic genetic markers suitable for genotyping sperm, eggs, and all life stages of the important agricultural pest, Anastrepha suspensa, have prevented detailed genetic studies of its breeding system, reproductive dynamics, and population dynamics. We describe polymerase chain reaction (PCR) primers and reaction conditions for amplifying nine polymorphic microsatellite DNA loci isolated from this species. The PCR primers were tested on four to five individuals each collected from five geographically distant locations in Florida. Heterozygosity values and the number of alleles per locus varied from 0.11 to 0.89, and from two to 12, respectively.     

Development and optimization of microsatellite DNA primers for boreal owls (Aegolius funereus)

We developed 22 microsatellite loci for boreal owls (Aegolius funereus). We genotyped 275 unrelated boreal owls (Aegolius f. richardsoni) and 36 unrelated Tengmalm's owls (Aegolius f. funereus) using seven loci that were polymorphic and did not have detectable null alleles. Among North American and Scandinavian boreal owls, respectively, allelic diversity ranged from three to 11 alleles and from one to 11 alleles, observed heterozygosity ranged from 0.31 to 0.80 and from 0.00 to 0.81, and expected heterozygosity ranged from 0.28 to 0.81 and from 0.00 to 0.81. These markers appeared to amplify DNA in six other Strigidae species.