Search results for "SPECIES RICHNESS"
showing 10 items of 427 documents
Burrows-Wheeler transform and palindromic richness
2009
AbstractThe investigation of the extremal case of the Burrows–Wheeler transform leads to study the words w over an ordered alphabet A={a1,a2,…,ak}, with a1<a2<⋯<ak, such that bwt(w) is of the form aknkak−1nk−1⋯a2n2a1n1, for some non-negative integers n1,n2,…,nk. A characterization of these words in the case |A|=2 has been given in [Sabrina Mantaci, Antonio Restivo, Marinella Sciortino, Burrows-Wheeler transform and Sturmian words, Information Processing Letters 86 (2003) 241–246], where it is proved that they correspond to the powers of conjugates of standard words. The case |A|=3 has been settled in [Jamie Simpson, Simon J. Puglisi, Words with simple Burrows-Wheeler transforms, Electronic …
The effect of automated taxa identification errors on biological indices
2017
In benthic macroinvertebrate biomonitoring systems, the target is to determine the status of ecosystems based on several biological indices. To increase cost-efficiency, computer-based taxa identification for image data has recently been developed. Taxa identification errors can, however, have strong effects on the indices and thus on the determination of the ecological status. In order to shift the biomonitoring process towards automated expert systems, we need a clear understanding on the bias caused by automation. In this paper, we examine eleven classification methods in the case of macroinvertebrate image data and show how their classification errors propagate into different biological…
Community Turnover of Wood-Inhabiting Fungi across Hierarchical Spatial Scales
2014
For efficient use of conservation resources it is important to determine how species diversity changes across spatial scales. In many poorly known species groups little is known about at which spatial scales the conservation efforts should be focused. Here we examined how the community turnover of wood-inhabiting fungi is realised at three hierarchical levels, and how much of community variation is explained by variation in resource composition and spatial proximity. The hierarchical study design consisted of management type (fixed factor), forest site (random factor, nested within management type) and study plots (randomly placed plots within each study site). To examine how species richne…
Conservation implications of species–genetic diversity correlations
2014
Despite its importance for the long-term viability of populations and functioning of ecosystems, the genetic diversity of populations is seldom given explicit consideration in conservation prioritization. Research on the species–genetic diversity correlation (SGDC) suggests that species diversity within a community and intrapopulation genetic diversity are positively correlated, due to the parallel influences of environmental characteristics (area, connectivity, and environmental heterogeneity) on both levels of diversity. A positive locality scale SGDC (i.e. α-SGDC) thus provides potential for simultaneous conservation of both species diversity within a locality and intrapopulation genetic…
The effect of peatland drainage and restoration on Odonata species richness and abundance
2015
Background Restoration aims at reversing the trend of habitat degradation, the major threat to biodiversity. In Finland, more than half of the original peatland area has been drained, and during recent years, restoration of some of the drained peatlands has been accomplished. Short-term effects of the restoration on peatland hydrology, chemistry and vegetation are promising but little is known about how other species groups apart from vascular plants and bryophytes respond to restoration efforts. Results Here, we studied how abundance and species richness of Odonata (dragonflies and damselflies) respond to restoration. We sampled larvae in three sites (restored, drained, pristine) on each o…
The role of power line rights-of-way as an alternative habitat for declined mire butterflies
2011
Habitat loss is one of the greatest threats for biodiversity. In Finland, two thirds of natural mires have been drained for silviculture, which transforms open wetlands into dense forests. However, vegetation management of power line rights-of-way (ROW) maintain the drained mires as open areas. The aim of this study was to determine the effect of the power line ROW vegetation management on butterfly abundance, species richness and community structure by comparing the managed power line ROWs to unmanaged drained control sites and to natural mires. The species richness or abundance of mire butterflies did not differ between the power line ROWs and natural mires. In contrast, both species rich…
Semi-natural habitats in the European boreal region: Caught in the socio-ecological extinction vortex?
2022
AbstractWe propose to consider semi-natural habitats—hotspots for biodiversity—being caught in a socio-ecological extinction vortex, similar to the phenomenon described for species threatened with extinction. These habitats are essentially socioecological systems, in which socioeconomic drivers are interlinked with ecological processes. We identify four highly interlinked and mutually reinforcing socio-economic processes, pertaining to the importance of semi-natural habitats for (i) agricultural production, (ii) policy, research and development; (iii) vocational education in the fields of agricultural sciences and (iv) public’s experiences with semi-natural habitats. Evidence from six count…
Perceptual presence without counterfactual richness
2014
In this commentary, I suggest that non-visual perceptual modalities provide counterexamples to Seth's claim that perceptual presence depends on counterfactual richness. Then I suggest a modification to Seth's view that is not vulnerable to these counterexamples.
Rodents and insectivores from the Lower Miocene (Agenian and Ramblian) of the Tudela Formation (Ebro Basin, Spain)
2012
The rodent and insectivore faunas of Agenian and Ramblian age from the Tudela Formation (Ebro Basin, Spain) are described. Four of the localities (CH1, CA1, CC1 and CA2) contain rodent remains of Agenian age (local zone Y), and three (CA3, CA3B and CA4) of Ramblian age (local zones Z and A). Typical Agenian taxa include Armantomys cf. bijmai (CH1), Eucricetodon cf. gerandianus (CA1), Peridyromys turbatus, Simplomys aff. aljaphi and Armantomys daamsi (CA2) and Eucricetodon aff. aquitanicus (CC1). On the other hand, some typical Ramblian taxa are Armantomys cf. parsani (CA3), Ligerimys aff. magnus and Pseudotheridomys sp. (CA4) and Prodryomys cf. brailloni (CA3B). The faunas are characterized…
Towards understanding the abundance of non-pollen palynomorphs : A comparison of fossil algae, algal pigments and sedaDNA from temperate lake sedimen…
2018
Given the increased interest in non-pollen palynomorphs (microscopic objects other than pollen identified from pollen slides) in palaeoecological studies, it is necessary to seek a deeper understanding of the reliability of these results. We combined quantitative information of algal pigments and sedimentary ancient DNA (sedaDNA) of phylotaxonomical resolution to validate the richness and abundance of fossil algae in the sediment of a small temperate lake. For the first time, fossil and sedaDNA algae data were combined in a composite data-set and used to reconstruct algae turnover rates over the last 14,500 years. This comparison serves as both an example of howfossil algae can be used to a…