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Feeding damage of Japanese beetle (Col.: Scarabaeidae) on 16 field-grown birch (Betula L.) genotypes
Feeding damage by Japanese beetle ( Popillia japonica Newman) was evaluated on 16 field-grown birch genotypes ( Betula L.) under two irrigation regimes at Fayetteville, AR in 2003, 2004 and 2005. Percentage of total leaf area skeletonized by Japanese beetle was visually estimated, and leaf damage was rated as no damage, low damage, moderate or severe damage based on the percentage of leaf skeletonization. The average percentage of leaf skeletonization on all birch trees by Japanese beetles was 32% in 2003, 27% in 2004 and 25% in 2005. In 2005, well-watered trees had a higher percentage of leaf skeletonization than water-stressed trees. Betula utilis var. jacquemontii and Betula papyrifera 'Uenci', rated as severe damage in all 3 years, were estimated to have the highest percentage of leaf skeletonization followed by B. papyrifera , which was rated as moderate-to-severe damage. Betula maximowicziana , Betula nigra 'Cully', B. papyrifera 'Renci', and Betula platyphylla 'Fargo' were rated as low-to-moderate damage. Betula pendula 'Laciniata' had nearly no damage from Japanese beetle in all 3 years. The other birch genotypes were rated as low damage during the 3-year period. 相似文献
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Adam C. Vandergriff Michael Taylor Hensley Ke Cheng 《Journal of visualized experiments : JoVE》2015,(98)
Cell culture has become increasingly important in cardiac research, but due to the limited proliferation of cardiomyocytes, culturing cardiomyocytes is difficult and time consuming. The most commonly used cells are neonatal rat cardiomyocytes (NRCMs), which require isolation every time cells are needed. The birth of the rats can be unpredictable. Cryopreservation is proposed to allow for cells to be stored until needed, yet freezing/thawing methods for primary cardiomyocytes are challenging due to the sensitivity of the cells. Using the proper cryoprotectant, dimethyl sulfoxide (DMSO), cryopreservation was achieved. By slowly extracting the DMSO while thawing the cells, cultures were obtained with viable NRCMs. NRCM phenotype was verified using immunocytochemistry staining for α-sarcomeric actinin. In addition, cells also showed spontaneous contraction after several days in culture. Cell viability after thawing was acceptable at 40-60%. In spite of this, the methods outlined allow one to easily cryopreserve and thaw NRCMs. This gives researchers a greater amount of flexibility in planning experiments as well as reducing the use of animals. 相似文献
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Melanie F. Struve Kevin W. Gaido Janan B. Hensley Kim P. Lehmann Susan M. Ross Mark A. Sochaski Gabrielle A. Willson David C. Dorman 《Birth defects research. Part B, Developmental and reproductive toxicology》2009,86(4):345-354
Most rodent developmental toxicity studies of dibutylphthalate (DBP) have relied on bolus gavage dosing. This study characterized the developmental toxicity of dietary DBP. Pregnant CD rats were given nominal doses of 0, 100, or 500 mg DBP/kg/day in diet (actual intake 0, 112, and 582 mg/kg/day) from gestational day (GD) 12 through the morning of GD 19. Rats were killed 4 or 24 hr thereafter. DBP dietary exposure resulted in significant dose-dependent reductions in testicular mRNA concentration of scavenger receptor class B, member 1; steroidogenic acute regulatory protein; cytochrome P450, family 11, subfamily a, polypeptide 1; and cytochrome P450 family 17, subfamily a, polypeptide 1. These effects were most pronounced 4 hr after the end of exposure. Testicular testosterone was reduced 24 hr post-exposure in both DBP dose groups and 4 hr after termination of the 500-mg DBP/kg/day exposure. Maternal exposure to 500 mg DBP/kg/day induced a significant reduction in male offspring's anogenital distance indicating in utero disruption of androgen function. Leydig cell aggregates, increased cord diameters, and multinucleated gonocytes were present in DBP-treated rats. Monobutyl phthalate, the developmentally toxic metabolite of DBP, and its glucuronide conjugate were found in maternal and fetal plasma, amniotic fluid, and maternal urine. Our results, when compared to previously conducted gavage studies, indicate that approximately equal doses of oral DBP exposure of pregnant rats, from diet or gavage, result in similar responses in male offspring. Birth Defects Res (Part B), 86:345–354, 2009. © 2009 Wiley-Liss, Inc. 相似文献