@article{SchittkoBernardVerdierHegeretal.2020,
  author    = {Schittko, Conrad and Bernard-Verdier, Maud and Heger, Tina and Buchholz, Sascha and Kowarik, Ingo and von der Lippe, Moritz and Seitz, Birgit and Joshi, Jasmin Radha and Jeschke, Jonathan M.},
  title     = {A multidimensional framework for measuring biotic novelty: How novel is a community?},
  series = {Global Change Biology},
  volume    = {26},
  journal   = {Global Change Biology},
  number    = {8},
  publisher = {John Wiley \& Sons, Inc.},
  address   = {New Jersey},
  pages     = {17},
  year      = {2020},
  abstract  = {Anthropogenic changes in climate, land use, and disturbance regimes, as well as introductions of non-native species can lead to the transformation of many ecosystems. The resulting novel ecosystems are usually characterized by species assemblages that have not occurred previously in a given area. Quantifying the ecological novelty of communities (i.e., biotic novelty) would enhance the understanding of environmental change. However, quantification remains challenging since current novelty metrics, such as the number and/or proportion of non-native species in a community, fall short of considering both functional and evolutionary aspects of biotic novelty. Here, we propose the Biotic Novelty Index (BNI), an intuitive and flexible multidimensional measure that combines (a) functional differences between native and non-native introduced species with (b) temporal dynamics of species introductions. We show that the BNI is an additive partition of Rao's quadratic entropy, capturing the novel interaction component of the community's functional diversity. Simulations show that the index varies predictably with the relative amount of functional novelty added by recently arrived species, and they illustrate the need to provide an additional standardized version of the index. We present a detailed R code and two applications of the BNI by (a) measuring changes of biotic novelty of dry grassland plant communities along an urbanization gradient in a metropolitan region and (b) determining the biotic novelty of plant species assemblages at a national scale. The results illustrate the applicability of the index across scales and its flexibility in the use of data of different quality. Both case studies revealed strong connections between biotic novelty and increasing urbanization, a measure of abiotic novelty. We conclude that the BNI framework may help building a basis for better understanding the ecological and evolutionary consequences of global change.},
  language  = {en}
}
@misc{JaricHegerMonzonetal.2019,
  author    = {Jaric, Ivan and Heger, Tina and Monzon, Federico Castro and Jeschke, Jonathan M. and Kowarik, Ingo and McConkey, Kim R. and Pysek, Petr and Sagouis, Alban and Essl, Franz},
  title     = {Crypticity in Biological Invasions},
  series = {Trends in Ecology \& Evolution},
  volume    = {34},
  journal   = {Trends in Ecology \& Evolution},
  number    = {4},
  publisher = {Elsevier},
  address   = {London},
  issn      = {0169-5347},
  doi       = {10.1016/j.tree.2018.12.008},
  pages     = {291 -- 302},
  year      = {2019},
  abstract  = {Ecological effects of alien species can be dramatic, but management and prevention of negative impacts are often hindered by crypticity of the species or their ecological functions. Ecological functions can change dramatically over time, or manifest after long periods of an innocuous presence. Such cryptic processes may lead to an underestimation of long-term impacts and constrain management effectiveness. Here, we present a conceptual framework of crypticity in biological invasions. We identify the underlying mechanisms, provide evidence of their importance, and illustrate this phenomenon with case studies. This framework has potential to improve the recognition of the full risks and impacts of invasive species.},
  language  = {en}
}
@article{vonderLippeBullockKowariketal.2013,
  author    = {von der Lippe, Moritz and Bullock, James M. and Kowarik, Ingo and Knopp, Tatjana and Wichmann, Matthias},
  title     = {Human-mediated dispersal of seeds by the airflow of vehicles},
  series = {PLoS one},
  volume    = {8},
  journal   = {PLoS one},
  number    = {1},
  publisher = {PLoS},
  address   = {San Fransisco},
  issn      = {1932-6203},
  doi       = {10.1371/journal.pone.0052733},
  pages     = {10},
  year      = {2013},
  abstract  = {Human-mediated dispersal is known as an important driver of long-distance dispersal for plants but underlying mechanisms have rarely been assessed. Road corridors function as routes of secondary dispersal for many plant species but the extent to which vehicles support this process remains unclear. In this paper we quantify dispersal distances and seed deposition of plant species moved over the ground by the slipstream of passing cars. We exposed marked seeds of four species on a section of road and drove a car along the road at a speed of 48 km/h. By tracking seeds we quantified movement parallel as well as lateral to the road, resulting dispersal kernels, and the effect of repeated vehicle passes. Median distances travelled by seeds along the road were about eight meters for species with wind dispersal morphologies and one meter for species without such adaptations. Airflow created by the car lifted seeds and resulted in longitudinal dispersal. Single seeds reached our maximum measuring distance of 45 m and for some species exceeded distances under primary dispersal. Mathematical models were fit to dispersal kernels. The incremental effect of passing vehicles on longitudinal dispersal decreased with increasing number of passes as seeds accumulated at road verges. We conclude that dispersal by vehicle airflow facilitates seed movement along roads and accumulation of seeds in roadside habitats. Dispersal by vehicle airflow can aid the spread of plant species and thus has wide implications for roadside ecology, invasion biology and nature conservation.},
  language  = {en}
}
@article{SchulzVoigtBeuschetal.2016,
  author    = {Schulz, Katharina and Voigt, Karsten and Beusch, Christine and Almeida-Cortez, Jarcilene S. and Kowarik, Ingo and Walz, Ariane and Cierjacks, Arne},
  title     = {Grazing deteriorates the soil carbon stocks of Caatinga forest ecosystems in Brazil},
  series = {Forest ecology and management},
  volume    = {367},
  journal   = {Forest ecology and management},
  publisher = {Elsevier},
  address   = {Amsterdam},
  issn      = {0378-1127},
  doi       = {10.1016/j.foreco.2016.02.011},
  pages     = {62 -- 70},
  year      = {2016},
  abstract  = {Grazing by domestic ungulates can have substantial impacts on forests in arid and semi-arid regions, possibly including severe loss of carbon from the soil. Predicting net livestock impacts on soil organic carbon stocks remains challenging, however, due to the dependence on animal loads and on soil and environmental parameters. The objective of this study was to better understand grazing effects on soil organic carbon in seasonal tropical dry forests of north-eastern Brazil (Caatinga) by quantifying carbon stocks of the upper soil profile (0-5 cm depth) and greater soil depths (>5 cm depth down to bedrock) along a gradient of grazing intensity while accounting for other influencing factors such as soil texture, vegetation, landscape topography, and water availability. We analysed soil organic carbon, soil clay content, altitude above sea level, soil depth to bedrock, distance to the nearest permanent water body, species diversity of perennial plants and aboveground biomass on 45 study plots located in the vicinity of the Itaparica Reservoir, Pernambuco, Brazil. Livestock (mainly goats and cattle) are unevenly distributed in the studied ecosystem, thus grazing intensity was accounted for based on the weight of livestock droppings per square metre and classified as no or light, intermediate, or heavy grazing. The mean soil organic carbon in the area was 16.86 ± 1.28 Mg ha\&\#8722;1 C with approximately one-quarter found in the upper 5 cm of the soil profile (4.14 ± 0.43 Mg ha\&\#8722;1 C) and the remainder (12.57 ± 0.97 Mg ha\&\#8722;1 C) in greater soil depths (>5 cm). Heavy grazing led to significantly lower soil organic carbon stocks in the upper 5 cm, whereas no effect on soil organic carbon of the soil overall or in greater soil depths was detectable. The soil's clay content and the altitude proved to be the most relevant factors influencing overall soil organic carbon stocks and those in greater soil depths (>5 cm). Our findings suggest that grazing causes substantial release of carbon from Brazilian dry forest soils, which should be addressed through improved grazing management via a legally compulsory rotation system. This would ultimately contribute to the conservation of a unique forest system and associated ecosystem services.},
  language  = {en}
}
@article{HornHempelRistowetal.2015,
  author    = {Horn, Sebastian and Hempel, Stefan and Ristow, Michael and Rillig, Matthias C. and Kowarik, Ingo and Caruso, Tancredi},
  title     = {Plant community assembly at small scales: Spatial vs. environmental factors in a European grassland},
  series = {Acta oecologica : international journal of ecology},
  volume    = {63},
  journal   = {Acta oecologica : international journal of ecology},
  publisher = {Elsevier},
  address   = {Paris},
  issn      = {1146-609X},
  doi       = {10.1016/j.actao.2015.01.004},
  pages     = {56 -- 62},
  year      = {2015},
  abstract  = {Dispersal limitation and environmental conditions are crucial drivers of plant species distribution and establishment. As these factors operate at different spatial scales, we asked: Do the environmental factors known to determine community assembly at broad scales operate at fine scales (few meters)? How much do these factors account for community variation at fine scales? In which way do biotic and abiotic interactions drive changes in species composition? We surveyed the plant community within a dry grassland along a very steep gradient of soil characteristics like pH and nutrients. We used a spatially explicit sampling design, based on three replicated macroplots of 15 x 15, 12 x 12 and 12 x 12 m in extent. Soil samples were taken to quantify several soil properties (carbon, nitrogen, plant available phosphorus, pH, water content and dehydrogenase activity as a proxy for overall microbial activity). We performed variance partitioning to assess the effect of these variables on plant composition and statistically controlled for spatial autocorrelation via eigenvector mapping. We also applied null model analysis to test for non-random patterns in species co-occurrence using randomization schemes that account for patterns expected under species interactions. At a fine spatial scale, environmental factors explained 18\% of variation when controlling for spatial autocorrelation in the distribution of plant species, whereas purely spatial processes accounted for 14\% variation. Null model analysis showed that species spatially segregated in a non-random way and these spatial patterns could be due to a combination of environmental filtering and biotic interactions. Our grassland study suggests that environmental factors found to be directly relevant in broad scale studies are present also at small scales, but are supplemented by spatial processes and more direct interactions like competition. (C) 2015 Elsevier Masson SAS. All rights reserved.},
  language  = {en}
}
@unpublished{CierjacksKowarikJoshietal.2013,
  author    = {Cierjacks, Arne and Kowarik, Ingo and Joshi, Jasmin Radha and Hempel, Stefan and Ristow, Michael and von der Lippe, Moritz and Weber, Ewald},
  title     = {Biological flora of the british isles: robinia pseudoacacia},
  series = {The journal of ecology},
  volume    = {101},
  journal   = {The journal of ecology},
  number    = {6},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0022-0477},
  doi       = {10.1111/1365-2745.12162},
  pages     = {1623 -- 1640},
  year      = {2013},
  abstract  = {This account presents information on all aspects of the biology of Robinia pseudoacacia L. that are relevant to understanding its ecological characteristics and behaviour. The main topics are presented within the standard framework of the Biological Flora of the British Isles: distribution, habitat, communities, responses to biotic factors, responses to environment, structure and physiology, phenology, floral and seed characters, herbivores and disease, and history and conservation.Robinia pseudoacacia, false acacia or black locust, is a deciduous, broad-leaved tree native to North America. The medium-sized, fast-growing tree is armed with spines, and extensively suckering. It has become naturalized in grassland, semi-natural woodlands and urban habitats. The tree is common in the south of the British Isles and in many other regions of Europe.Robinia pseudoacacia is a light-demanding pioneer species, which occurs primarily in disturbed sites on fertile to poor soils. The tree does not tolerate wet or compacted soils. In contrast to its native range, where it rapidly colonizes forest gaps and is replaced after 15-30years by more competitive tree species, populations in the secondary range can persist for a longer time, probably due to release from natural enemies.Robinia pseudoacacia reproduces sexually, and asexually by underground runners. Disturbance favours clonal growth and leads to an increase in the number of ramets. Mechanical stem damage and fires also lead to increased clonal recruitment. The tree benefits from di-nitrogen fixation associated with symbiotic rhizobia in root nodules. Estimated symbiotic nitrogen fixation rates range widely from 23 to 300kgha(-1)year(-1). The nitrogen becomes available to other plants mainly by the rapid decay of nitrogen-rich leaves.Robinia pseudoacacia is host to a wide range of fungi both in the native and introduced ranges. Megaherbivores are of minor significance in Europe but browsing by ungulates occurs in the native range. Among insects, the North American black locust gall midge (Obolodiplosis robiniae) is specific to Robinia and is spreading rapidly throughout Europe. In parts of Europe, Robinia pseudoacacia is considered an invasive non-indigenous plant and the tree is controlled. Negative impacts include shading and changes of soil conditions as a result of nitrogen fixation.},
  language  = {en}
}
@misc{SchittkoBernardVerdierHegeretal.2020,
  author    = {Schittko, Conrad and Bernard-Verdier, Maud and Heger, Tina and Buchholz, Sascha and Kowarik, Ingo and von der Lippe, Moritz and Seitz, Birgit and Joshi, Jasmin Radha and Jeschke, Jonathan M.},
  title     = {A multidimensional framework for measuring biotic novelty: How novel is a community?},
  series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe},
  journal   = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe},
  number    = {8},
  issn      = {1866-8372},
  doi       = {10.25932/publishup-52565},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-525657},
  pages     = {19},
  year      = {2020},
  abstract  = {Anthropogenic changes in climate, land use, and disturbance regimes, as well as introductions of non-native species can lead to the transformation of many ecosystems. The resulting novel ecosystems are usually characterized by species assemblages that have not occurred previously in a given area. Quantifying the ecological novelty of communities (i.e., biotic novelty) would enhance the understanding of environmental change. However, quantification remains challenging since current novelty metrics, such as the number and/or proportion of non-native species in a community, fall short of considering both functional and evolutionary aspects of biotic novelty. Here, we propose the Biotic Novelty Index (BNI), an intuitive and flexible multidimensional measure that combines (a) functional differences between native and non-native introduced species with (b) temporal dynamics of species introductions. We show that the BNI is an additive partition of Rao's quadratic entropy, capturing the novel interaction component of the community's functional diversity. Simulations show that the index varies predictably with the relative amount of functional novelty added by recently arrived species, and they illustrate the need to provide an additional standardized version of the index. We present a detailed R code and two applications of the BNI by (a) measuring changes of biotic novelty of dry grassland plant communities along an urbanization gradient in a metropolitan region and (b) determining the biotic novelty of plant species assemblages at a national scale. The results illustrate the applicability of the index across scales and its flexibility in the use of data of different quality. Both case studies revealed strong connections between biotic novelty and increasing urbanization, a measure of abiotic novelty. We conclude that the BNI framework may help building a basis for better understanding the ecological and evolutionary consequences of global change.},
  language  = {en}
}
@article{HegerBernardVerdierGessleretal.2019,
  author    = {Heger, Tina and Bernard-Verdier, Maud and Gessler, Arthur and Greenwood, Alex D. and Grossart, Hans-Peter and Hilker, Monika and Keinath, Silvia and Kowarik, Ingo and K{\"u}ffer, Christoph and Marquard, Elisabeth and Mueller, Johannes and Niemeier, Stephanie and Onandia, Gabriela and Petermann, Jana S. and Rillig, Matthias C. and Rodel, Mark-Oliver and Saul, Wolf-Christian and Schittko, Conrad and Tockner, Klement and Joshi, Jasmin Radha and Jeschke, Jonathan M.},
  title     = {Towards an Integrative, Eco-Evolutionary Understanding of Ecological Novelty: Studying and Communicating Interlinked Effects of Global Change},
  series = {Bioscience},
  volume    = {69},
  journal   = {Bioscience},
  number    = {11},
  publisher = {Oxford Univ. Press},
  address   = {Oxford},
  issn      = {0006-3568},
  doi       = {10.1093/biosci/biz095},
  pages     = {888 -- 899},
  year      = {2019},
  abstract  = {Global change has complex eco-evolutionary consequences for organisms and ecosystems, but related concepts (e.g., novel ecosystems) do not cover their full range. Here we propose an umbrella concept of "ecological novelty" comprising (1) a site-specific and (2) an organism-centered, eco-evolutionary perspective. Under this umbrella, complementary options for studying and communicating effects of global change on organisms, ecosystems, and landscapes can be included in a toolbox. This allows researchers to address ecological novelty from different perspectives, e.g., by defining it based on (a) categorical or continuous measures, (b) reference conditions related to sites or organisms, and (c) types of human activities. We suggest striving for a descriptive, non-normative usage of the term "ecological novelty" in science. Normative evaluations and decisions about conservation policies or management are important, but require additional societal processes and engagement with multiple stakeholders.},
  language  = {en}
}