scholarly journals Ovipositional Behavior of the Egg Parasitoid Gryon pennsylvanicum (Hymenoptera: Scelionidae) on Two Squash Bug Species Anasa tristis (Hemiptera: Coreidae) and Anasa armigera: Effects of Parasitoid Density, Nutrition, and Host Egg Chorion on Parasitism Rates

2020 ◽  
Vol 49 (6) ◽  
pp. 1307-1315
Author(s):  
Mary L Cornelius ◽  
Bryan T Vinyard ◽  
Joseph D Mowery ◽  
Jing S Hu
Keyword(s):  
Electron Microscopy ◽  
Laboratory Tests ◽  
Egg Parasitoid ◽  
Egg Masses ◽  
Anasa Tristis ◽  
Ovipositional Behavior ◽  
Squash Bug ◽  
Percent Parasitism ◽  
Transmission Electron ◽  
Parasitism Rates

Abstract This study examined the ovipositional behavior of Gryon pennsylvanicum Ashmead (Hymenoptera: Scelionidae) on egg masses of two squash bug species Anasa tristis DeGeer and Anasa armigera Say (Hemiptera: Coreidae) by evaluating how parasitoid density and access to nutrition influenced percent parasitism on egg masses of different sizes in laboratory tests. When three parasitoids were exposed to A. tristis egg masses with only three to five eggs, 72.7% of parasitoids became trapped in the eggs and failed to emerge successfully. These results suggest that competition between larvae within the egg may have reduced the fitness of the surviving parasitoid. Continual access to honey water did not significantly influence parasitism rates on A. armigera egg masses and only increased parasitism on A. tristis egg masses with 20–25 eggs. Overall, parasitism rates were higher on A. armigera egg masses than on A. tristis egg masses, and parasitoids were more likely to emerge successfully from A. armigera eggs than from A. tristis eggs. Parasitoids spent the same amount of time probing eggs of the two species, but they spent significantly more time drilling into A. tristis eggs than A. armigera eggs. Measurements taken using transmission electron microscopy determined that the average combined width of the epicuticle and exocuticle of the egg chorion was significantly greater for A. tristis eggs than for A. armigera eggs. This difference may account for the lower rates of parasitism and parasitoid emergence and for the increased time spent drilling into A. tristis eggs compared with A. armigera eggs.

scholarly journals Use of Flowering Plants to Enhance Parasitism and Predation Rates on Two Squash Bug Species Anasa tristis and Anasa armigera (Hemiptera: Coreidae)

Insects ◽  
2019 ◽  
Vol 10 (10) ◽  
pp. 318 ◽  
Author(s):  
Cornelius ◽  
Vinyard ◽  
Gates
Keyword(s):  
Egg Parasitoid ◽  
Egg Masses ◽  
Anasa Tristis ◽  
Future Studies ◽  
Squash Bug ◽  
Parasitism Rates ◽  
Adult Parasitoid ◽  
Egg Parasitism ◽  
Fagopyrum Esculentum Moench ◽  
Predation Rates

A two-year study evaluated the effect of a flowering border of buckwheat Fagopyrum esculentum Moench on rates of egg parasitism, egg predation and adult parasitism on two squash bug species, Anasa tristis (DeGeer) and Anasa armigera Say, by comparing rates in squash fields with and without a flowering border. Furthermore, we evaluated whether there was an edge effect by comparing parasitism and predation rates in plots located in the corner of a squash field with plots located in the center of a squash field for fields with and without a flowering border. The egg parasitism rates were not affected by either treatment (flowering border or control) or plot location (edge or center). Anasa armigera egg masses only accounted for 4.3% of the total egg masses collected. The egg parasitism rates increased gradually throughout the season, peaking in the last week of August in 2017 at 45% for A. tristis egg masses. The most common egg parasitoid recovered was Gryon pennsylvanicum (Ashmead) followed by Ooencyrtus anasae (Ashmead). Adult parasitism was not affected by treatment, but A. tristis adult parasitism rates were higher in plots located on the edge of squash fields compared with plots located in the center of squash fields in 2016. Since adult parasitoid, Trichopoda pennipes (Fabricius) flies were observed visiting buckwheat flowers, future studies could explore the possibility that the flowering buckwheat may have a more impact on adult parasitism if there was a greater distance between fields with and without a flowering border.

scholarly journals Impact of the Egg Parasitoid,Gryon pennsylvanicum(Hymenoptera: Scelionidae), on Sentinel and Wild Egg Masses of the Squash Bug (Hemiptera: Coreidae) in Maryland

2016 ◽  
Vol 45 (2) ◽  
pp. 367-375 ◽  
Author(s):  
Mary L. Cornelius ◽  
Matthew L. Buffington ◽  
Elijah J. Talamas ◽  
Michael W. Gates
Keyword(s):  
Egg Parasitoid ◽  
Egg Masses ◽  
Squash Bug

scholarly journals Exploratory Survey of Spotted Lanternfly (Hemiptera: Fulgoridae) and Its Natural Enemies in China

2020 ◽  
Author(s):  
Bei Xin ◽  
Yan-long Zhang ◽  
Xiao-yi Wang ◽  
Liang-ming Cao ◽  
Kim A Hoelmer ◽  
...  
Keyword(s):  
Natural Enemies ◽  
Host Plants ◽  
Egg Parasitoid ◽  
Shaanxi Province ◽  
Western China ◽  
Beijing City ◽  
Egg Masses ◽  
Parasitism Rates ◽  
Lycorma Delicatula ◽  
Biocontrol Program

Abstract An invasive population of spotted lanternfly (SLF), Lycorma delicatula White, was first noted in North America in Pennsylvania in 2014, and by September 2020 populations had spread to six additional states. To develop a biocontrol program to aid in the management of the pest, exploratory surveys for SLF natural enemies in its native range were carried out in 27 provinces and other administrative regions of China from 2015 to 2019. Naturally laid egg masses were collected and sentinel SLF egg masses were deployed to attract egg parasitoids, and yellow sticky traps were used to collect SLF nymphs to discover and determine the parasitism rates of nymphal parasitoids. Results show that SLF is widely distributed in China (22 provinces and regions) and that the population densities in northeast China are higher than in southern and western China. An egg parasitoid, Anastatus orientalis Yang (Hymenoptera: Eupelmidae), and a nymphal parasitoid, Dryinus sinicus Olmi (Hymenoptera: Dryinidae), were collected. Anastatus orientalis was reared from SLF eggs in seven provinces in China with parasitoid emergence rates ranging from 4.0 to 15.5% (or 17.6 to 37.3% if including only egg masses that had at least some parasitism). There were significant differences in parasitoid emergence rates between sites associated with factors including habitat and host plants. Dryinus sinicus was discovered in eight cities across six provinces. The percentage of SLF nymphs parasitized by D. sinicus were 31.1, 23.3, and 0% in Tai’an, Shandong Province, Beijing City, and Yan’an, Shaanxi Province, respectively. These two parasitoids are promising natural enemies that are being considered as potential biocontrol agents of invasive populations of SLF.

scholarly journals Simulation of Natural Corrosion by Vapor Hydration Test: Seven-Year Results

1996 ◽  
Vol 465 ◽  
Author(s):  
J. S. Luo ◽  
W. L. Ebert ◽  
J. J. Mazer ◽  
J. K. Bates
Keyword(s):  
Electron Microscopy ◽  
Water Vapor ◽  
Laboratory Tests ◽  
Basaltic Glass ◽  
X Ray ◽  
Corrosion Kinetics ◽  
Transmission Electron ◽  
Corrosion Reaction ◽  
Time Periods ◽  
Natural Corrosion

ABSTRACTWe have investigated the alteration behavior of synthetic basalt and SRL 165 borosilicate waste glasses that had been reacted in water vapor at 70°C for time periods up to seven years. The nature and extent of corrosion of glasses have been determined by characterizing the reacted glass surface with optical microscopy, scanning electron microscopy (SEM), transmission electron microscopy (SEM), and energy dispersive x-ray spectroscopy (EDS). Alteration in 70°C laboratory tests was compared to that which occurs at 150–200°C and also with Hawaiian basaltic glasses of 480 to 750 year old subaerially altered in nature. Synthetic basalt and waste glasses, both containing about 50 wt % SiO2, were found to react with water vapor to form an amorphous hydrated gel that contained small amounts of clay, nearly identical to palagonite layers formed on naturally altered basaltic glass. This result implies that the corrosion reaction in nature can be simulated with a vapor hydration test. These tests also provide a means for measuring the corrosion kinetics, which are difficult to determine by studying natural samples because alteration layers have often spalled off the samples and we have only limited knowledge of the conditions under which alteration occurred.

Techniques for Transmission Electron Microscopy of Fiber-Matrix Interfaces in Aluminum Alloy-Boron Composites by Ion Erosio

1971 ◽  
Vol 29 ◽  
pp. 204-205
Author(s):  
G. G. Shaw
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Aluminum Alloy ◽  
Electron Beam ◽  
Pure Aluminum ◽  
Ion Milling ◽  
Transmission Electron ◽  
Fiber Matrix ◽  
Ion Erosion ◽  
Row Of Fibers

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.

Direct Observation of Heat Exchanger Deposits by Cross Sectioning

1967 ◽  
Vol 25 ◽  
pp. 364-365
Author(s):  
R. W. Anderson ◽  
D. L. Senecal
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Heat Exchanger ◽  
Direct Observation ◽  
Cross Sections ◽  
Preparation Method ◽  
Specimen Preparation ◽  
Flowing Water ◽  
Transmission Electron ◽  
Deposit Layer

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.

Phase Transformations in Ti-7w/oMo-3w/oMe Alloy

1974 ◽  
Vol 32 ◽  
pp. 514-515
Author(s):  
S. Fujishiro
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Transmission Electron Microscopy ◽  
Tensile Strength ◽  
Mechanical Processing ◽  
Ray Method ◽  
X Ray ◽  
Transmission Electron ◽  
Water Quench ◽  
Alpha Beta

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.

Ultrastructural Analysis of the Salivary Glands of Gromphadorhina Portentosa (Schaum)

1977 ◽  
Vol 35 ◽  
pp. 638-639
Author(s):  
P.J. Dailey
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Salivary Glands ◽  
Secretory Vesicles ◽  
The Past ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Gromphadorhina Portentosa ◽  
Scanning Electron ◽  
Topographical Relief

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).

Transmission Electron Microscopy Studies of Pore Cells in Limax Maximus

1977 ◽  
Vol 35 ◽  
pp. 656-657
Author(s):  
B. S. Beltz
Keyword(s):  
Electron Microscopy ◽  
Cell Periphery ◽  
Salivary Duct ◽  
Terrestrial Mollusc ◽  
Buccal Ganglia ◽  
Transmission Electron ◽  
Pore Cells ◽  
Gland Tissue ◽  
Storage Area ◽  
Limax Maximus

The cells which are described in this study surround the salivary nerve of the terrestrial mollusc, Limax maximus. The salivary system of Limax consists of bilateral glands, ducts, and nerves. The salivary nerves originate at the buccal ganglia, which are situated on the posterior face of the buccal mass, and run along the salivary duct to the gland. The salivary nerve branches several times near the gland, and eventually sends processes into the gland.The pore cells begin to appear at the first large branch point of the salivary nerve, near the gland (Figure 1). They follow the nerve distally and eventually accompany the nerve branches into the gland tissue. The cells are 20-50 microns in diameter and contain very small nuclei (1-5 microns) (Figure 2).The cytoplasm of the pore cells is segregated into a storage area of glycogen and an organelle region located in a band around the cell periphery (Figure 3).

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