Predicting valuable forest habitats using an indicator species for biodiversity

Intensive management of boreal forests impairs forest biodiversity and species of old-growth forest. Effective measures to support biodiversity require detection of locations valuable for conservation. We applied species distribution models (SDMs) to a species of mature forest, the northern goshawk (Accipiter gentilis, goshawk), that is often associated with hotspots of forest biodiversity. We located optimal sites for the goshawk on a landscape scale, assessed their state under intensified logging operations and identified characteristics of goshawks' nesting sites in boreal forests. Optimal sites for the goshawk covered only 3.4% of the boreal landscape and were mostly located outside protected areas, which highlights the importance of conservation actions in privately-owned forests. Furthermore, optimal sites for the goshawk and associated biodiversity were under threat. Half of them were logged to some extent and 10% were already lost or notably deteriorated due to logging shortly after 2015 for which our models were calibrated. Habitat suitability for the goshawk increased with increasing volume of Norway spruce (Picea abies) peaking at 220 m(3) ha(-1), and with small quantities of birches (Betula spp.) and other broad-leaved trees. Threats to biodiversity of mature spruce forests are likely to accelerate in the future with increasing logging pressures and shorter rotation periods. Logging should be directed less to forests with high biodiversity. Continuous supply of mature spruce forests in the landscape should be secured with a denser network of protected areas and measures that aid in sparing large entities of mature forest on privately-owned land.peerReviewe

Pre-α-pro-GDNF and Pre-β-pro-GDNF Isoforms Are Neuroprotective in the 6-hydroxydopamine Rat Model of Parkinson's Disease

Glial cell line-derived neurotrophic factor (GDNF) is one of the most studied neurotrophic factors. GDNF has two splice isoforms, full-length pre-alpha-pro-GDNF (u-GDNF) and pre-beta-pro-GDNF (beta-GDNF), which has a 26 amino acid deletion in the pro-region. Thus far, studies have focused solely on the u-GDNF isoform, and nothing is known about the in vivo effects of the shorter beta-GDNF variant. Here we compare for the first time the effects of overexpressed cx-GDNF and beta-GDNF in non-lesioned rat striatum and the partial 6-hydroxydopamine lesion model of Parkinson's disease. GDNF isoforms were overexpressed with their native pre-pro-sequences in the striatum using an adeno-associated virus (AAV) vector, and the effects on motor performance and dopaminergic phenotype of the nigrostriatal pathway were assessed. In the non-lesioned striatum, both isoforms increased the density of dopamine transporter-positive fibers at 3 weeks after viral vector delivery. Although both isoforms increased the activity of the animals in cylinder assay, only u-GDNF enhanced the use of contralateral paw. Four weeks later, the striatal tyrosine hydroxylase (TH)-immunoreactivity was decreased in both u-GDNF and 1-GDNF treated animals. In the neuroprotection assay, both GDNF splice isoforms increased the number of TH-immunoreactive cells in the substantia nigra but did not promote behavioral recovery based on amphetamine-induced rotation or cylinder assays. Thus, the shorter GDNF isoform, beta-GDNF, and the full-length alpha-isoform have comparable neuroprotective efficacy on dopamine neurons of the nigrostriatal circuitry.Peer reviewe