Spatial patterns on the sagebrush steppe/Western juniper ecotone

Analysis of the spatial patterns of woody plants is important to better understand the ecological processes that govern the worldwide expansion of woody plants across semi-arid ecosystems. Second-order characteristics of a marked spatial point pattern of western juniper (Juniperus occidentalis subsp. occidentalis) were analyzed using Ripley’s K-functions and the pair-correlation function g. The marked point process of crown diameters was produced via two-dimensional wavelet analysis of a fine scale aerial photograph at the woodland-steppe ecotone in the Reynolds Creek watershed in the Owyhee Mountains, southwestern Idaho. Colonization of J. occidentalis stems from mature juniper trees growing in rocky, fire resistant areas. Although these areas introduce components of natural heterogeneity within the landscape, the selected study area is situated within a single soil type, and we modeled the expansion of juniper plants into previously juniper-free sagebrush steppe as a homogeneous point process with constant intensity. Through this research we have identified two statistically significant spatial scales characteristic of J. occidentalis on the woodland/steppe ecotone: (1) We observed inhibition between J. occidentalis plants at distances <15 m, resulting in a regular pattern, rather than clumped or random. This short-distance inhibition can be attributed to competition for water and other resources. Recruitment of young J. occidentalis occurs significantly more often in a direction away from older plants, maximizing the utilization of water and light resources, and perpetuating the spread of the species into previously juniper-free shrub-steppe. (2) J. occidentalis on the ecotone exhibits significant clustering within a 30–60 m radius. Bivariate point pattern analyses provide evidence that, within a distance of 50–70 m, there is a spatial dependence in tree size such that medium trees are more likely than small trees to be close to large trees. We attribute these phenomena to the fact that juniper seeds are commonly dispersed by berry-eating birds with small territories (0.3–1 ha). Beyond a distance of 50–70 m, juniper plants are randomly distributed, suggesting that additional long-range seed dispersal processes are at work. We further acknowledge the importance of including a reference to spatial scale when formulating hypotheses in statistical analysis of spatio-temporal point patterns.     

DNA barcoding the Lake Edward basin: high taxonomic coverage of a tropical freshwater ichthyofauna

Hydrobiologia - We present an extensive DNA barcoding study of the fish species of the Lake Edward system, including information on intraspecific variation. The DNA barcode gene, cytochrome c...     

Mating type‐dependent partner sensing as mediated by VEL1 in Trichoderma reesei

Sexual development in the filamentous model ascomycete Trichoderma reesei (syn. Hypocrea jecorina) was described only a few years ago. In this study, we show a novel role for VELVET in fungi, which links light response, development and secondary metabolism. Vel1 is required for mating in darkness, normal growth and conidiation. In light, vel1 was dispensable for male fertility but essential for female fertility in both mating types. VEL1 impacted regulation of the pheromone system (hpr1, hpr2, hpp1, ppg1) in a mating type‐dependent manner and depending on the mating partner of a given strain. These partner effects only occurred for hpp1 and hpr2, the pheromone precursor and receptor genes associated with the MAT1‐2 mating type and for the mating type gene mat1‐2‐1. Analysis of secondary metabolite patterns secreted by wild type and mutants under asexual and sexual conditions revealed that even in the wild type, the patterns change upon encounter of a mating partner, with again distinct differences for wild type and vel1 mutants. Hence, T. reesei applies a language of pheromones and secondary metabolites to communicate with mating partners and that this communication is at least in part mediated by VEL1.     

Multidomain Human Peroxidasin 1 Is a Highly Glycosylated and Stable Homotrimeric High Spin Ferric Peroxidase

Human peroxidasin 1 (hsPxd01) is a multidomain heme peroxidase that uses bromide as a cofactor for the formation of sulfilimine cross-links. The latter confers critical structural reinforcement to collagen IV scaffolds. Here, hsPxd01 and various truncated variants lacking nonenzymatic domains were recombinantly expressed in HEK cell lines. The N-glycosylation site occupancy and disulfide pattern, the oligomeric structure, and unfolding pathway are reported. The homotrimeric iron protein contains a covalently bound ferric high spin heme per subunit with a standard reduction potential of the Fe(III)/Fe(II) couple of −233 ± 5 mV at pH 7.0. Despite sequence homology at the active site and biophysical properties similar to human peroxidases, the catalytic efficiency of bromide oxidation (k_cat/K_M^app) of full-length hsPxd01 is rather low but increased upon truncation. This is discussed with respect to its structure and proposed biosynthetic function in collagen IV cross-linking.     

Differential effects of cyclophosphamide and mycophenolate mofetil on cellular and serological parameters in patients with systemic lupus erythematosus

IntroductionDisease activity and therapy show an impact on cellular and serological parameters in patients with systemic lupus erythematosus (SLE). This study was performed to compare the influence of mycophenolate mofetil (MMF) and cyclophosphamide (CYC) therapy on these parameters in patients with flaring, organ-threatening disease.MethodsSLE patients currently receiving CYC (n = 20), MMF (n = 25) or no immunosuppressive drugs (n = 22) were compared using a cross-sectional design. Median disease activity and daily corticosteroid dose were similar in these treatment groups. Concurrent medication, organ manifestations, and disease activity were recorded, and cellular and serological parameters were determined by routine diagnostic tests or flow cytometric analysis. In addition follow-up data were obtained from different sets of patients (CYC n = 24; MMF n = 23).ResultsAlthough both drugs showed a significant effect on disease activity and circulating B cell subsets, only MMF reduced circulating plasmablasts and plasma cells as well as circulating free light chains within three months of induction therapy. Neither MMF nor CYC were able to reduce circulating memory B cells. MMF lowered IgA levels more markedly than CYC. We did not observe a significant difference in the reduction of IgG levels or anti-dsDNA antibodies comparing patients receiving MMF or CYC. In contrast to MMF, induction therapy with CYC was associated with a significant increase of circulating CD8+ effector T cells and plasmacytoid dendritic cells (PDCs) after three months.ConclusionsThe results indicate differences between MMF and CYC with regard to the mechanism of action. MMF, but not CYC, treatment leads to a fast and enduring reduction of surrogate markers of B cell activation, such as circulating plasmablasts, plasma cells and free light chains but a comparable rate of hypogammaglobulinemia.

Electronic supplementary material

The online version of this article (doi:10.1186/s13075-015-0603-8) contains supplementary material, which is available to authorized users.