Cadmium adsorption on hydroxyaluminosilicate-montmorillonite complex as influenced by oxalate and citrate

The hydroxyaluminosilicate (HAS)-montmorillonite (Mt) and hydroxyaluminum (HyA)-Mt complexes are important constituents of soil colloidal complexes in acidic environments. Oxalate and citrate are dominant organic acids in the root exudates of many plants. These acids, among other factors, strongly influence the adsorption behavior of HAS-Mt and HyA-Mt complexes. In this study, we investigated the adsorption phenomena of Cd on the HAS-Mt and HyA-Mt complexes as influenced by oxalate and citrate. Without addition of oxalate and citrate, the adsorption of Cd on Mt was easy. However, in the presence of oxalate and citrate, the adsorption was strongly inhibited. In contrast, the HAS-Mt and HyA-Mt complexes in the absence of oxalate and citrate hardly adsorbed Cd. In the presence of oxalate, the HAS-Mt and HyA-Mt complexes were able to adsorb Cd. Thus, optimal concentration of oxalate for Cd adsorption on both complexes could be determined. Similarly, the HyA-Mt complex showed an optimal concentration of citrate for Cd adsorption. However, the HAS-Mt complex did not adsorb Cd in the presence of citrate. We concluded that the optimal concentrations of oxalate and citrate for Cd adsorption depended on the form of Cd ions and their proportion in the solution. Based on the amount of Cd adsorbed and the distribution of Cd species in the solution, the adsorption of Cd on the HAS-Mt and HyA-Mt complexes took place in various chemical forms.     

Greatwall phosphorylates an inhibitor of protein phosphatase 2A that is essential for mitosis

Entry into mitosis in eukaryotes requires the activity of cyclin-dependent kinase 1 (Cdk1). Cdk1 is opposed by protein phosphatases in two ways: They inhibit activation of Cdk1 by dephosphorylating the protein kinases Wee1 and Myt1 and the protein phosphatase Cdc25 (key regulators of Cdk1), and they also antagonize Cdk1's own phosphorylation of downstream targets. A particular form of protein phosphatase 2A (PP2A) containing a B55δ subunit (PP2A- B55δ) is the major protein phosphatase that acts on model CDK substrates in Xenopus egg extracts and has antimitotic activity. The activity of PP2A-B55δ is high in interphase and low in mitosis, exactly opposite that of Cdk1. We report that inhibition of PP2A-B55δ results from a small protein, known as α-endosulfine (Ensa), that is phosphorylated in mitosis by the protein kinase Greatwall (Gwl). This converts Ensa into a potent and specific inhibitor of PP2A-B55δ. This pathway represents a previously unknown element in the control of mitosis.     

Effects of a breeding scheme combined by genomic pre‐selection and progeny testing on annual genetic gain in a dairy cattle population

The effectiveness of the incorporation of genomic pre‐selection into dairy cattle progeny testing (GS‐PT) was compared with that of progeny testing (PT) where the fraction of dam to breed bull (DB) selected was 0.01. When the fraction of sires to breed bulls (SB) selected without being progeny tested to produce young bulls (YB) in the next generation was 0.2, the annual genetic gain from GS‐PT was 13% to 43% greater when h² = 0.3 and 16% to 53% greater when h² = 0.1 compared with that from PT. Given h² = 0.3, a selection accuracy of 0.8 for both YB and DB, and selected fractions of 0.117 for YB and 0.04 for DB, GS‐PT produced 40% to 43% greater annual genetic gain than PT. Given h² = 0.1, a selection accuracy of 0.6 for both YB and DB, and selected fractions of 0.117 for YB and 0.04 for DB, annual genetic gain from GS‐PT was 48% to 53% greater than that from PT. When h² = 0.3, progeny testing capacity had little effect on annual genetic gain from GS‐PT. However, when h² = 0.1, annual genetic gain from GS‐PT increased with increasing progeny testing capacity.     

Magnetic resonance imaging of a canine eye with melanoma

An 8-year-old Beagle dog had exophthalmos of the left eye for the last two past months. On ophthalmoscopy, the intraocular lesion could not be evaluated due to the opacity of the cornea. Ultrasonography revealed that the eyeball was distorted in shape and shifted in position, however, the precise lesion could not be identified. On magnetic resonance (MR) imaging, the lesion was observed as hyperintense on T1-weighted and hypointense on T2-weighted images, similar to those reported in human melanoma. The lesion was histologically diagnosed to be malignant intraocular melanoma. Though this is only a case report, canine ocular melanoma may show the similar characteristic MR images as in human uveal malignant melanoma.