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Journal articles on the topic 'Ecology of species distribution'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Sofronova, E. V., and A. D. Potemkin. "Four rare liverwort species: distribution, ecology, taxonomy." Novosti sistematiki nizshikh rastenii 52, no. 2 (2018): 505–18. http://dx.doi.org/10.31111/nsnr/2018.52.2.505.

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Distribution, ecology and taxonomy of four rare liverwort species Frullania davurica, Lejeunea alaskana, Marchantia romanica, Scapania sphaerifera, which were recorded many times in collections from the Republic of Sakha (Yakutia), are compiled and analyzed. Worldwide distribution maps of Lejeunea alaskana, Marchantia romanica, Scapania sphaerifera are provided. Taxonomic status of all four species needs to be tested on the basis of molecular studies of materials through their ranges. Sporophytes of Lejeunea alaskana are described for the first time.

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2

Godsoe, William. "Inferring the similarity of species distributions using Species’ Distribution Models." Ecography 37, no. 2 (2013): 130–36. http://dx.doi.org/10.1111/j.1600-0587.2013.00403.x.

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3

Keča, N., and H. Solheim. "Ecology and distribution of Armillaria species in Norway." Forest Pathology 41, no. 2 (2011): 120–32. http://dx.doi.org/10.1111/j.1439-0329.2010.00644.x.

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4

Tsopelas, By P. "Distribution and ecology of Armillaria species in Greece." Forest Pathology 29, no. 2 (1999): 103–16. http://dx.doi.org/10.1046/j.1439-0329.1999.00139.x.

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5

Parsons, P. A. "Geographical ecology. Patterns in the distribution of species." Endeavour 9, no. 1 (1985): 57. http://dx.doi.org/10.1016/0160-9327(85)90018-3.

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6

Fink, Daniel, Theodoros Damoulas, Nicholas E. Bruns, et al. "Crowdsourcing Meets Ecology: Hemisphere-Wide Spatiotemporal Species Distribution Models." AI Magazine 35, no. 2 (2014): 19–30. http://dx.doi.org/10.1609/aimag.v35i2.2533.

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Ecological systems are inherently complex. The processes that affect the distributions of animals and plants operate at multiple spatial and temporal scales, presenting a unique challenge for the development and coordination of effective conservation strategies, particularly for wide-ranging species. In order to study ecological systems across scales, data must be collected at fine resolutions across broad spatial and temporal extents. Crowdsourcing has emerged as an efficient way to gather these data by engaging large numbers of people to record observations. However, data gathered by crowdso

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7

Рерко, V. O., R. M. Sachuk, S. V. Zhyhaliuk, and I. T. Hulyk. "Helminthofauna of wild ungulates: ecology, species composition, distribution (review)." Bulletin "Veterinary biotechnology" 30 (2017): 183–95. http://dx.doi.org/10.31073/vet_biotech30-24.

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8

Connor, H. E., E. Edgar, and G. W. Bourdôt. "Ecology and distribution of naturalised species ofStipain New Zealand." New Zealand Journal of Agricultural Research 36, no. 3 (1993): 301–7. http://dx.doi.org/10.1080/00288233.1993.10417727.

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9

Scott, N. E., and A. W. Davison. "The distribution and ecology of coastal species on roadsides." Vegetatio 62, no. 1-3 (1985): 433–40. http://dx.doi.org/10.1007/bf00044771.

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10

França, Susana, and Henrique N. Cabral. "Predicting fish species distribution in estuaries: Influence of species’ ecology in model accuracy." Estuarine, Coastal and Shelf Science 180 (October 2016): 11–20. http://dx.doi.org/10.1016/j.ecss.2016.06.010.

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11

Gilbert, O. L., and O. W. Purvis. "Teloschistes Flavicans in Great Britain: Distribution and Ecology." Lichenologist 28, no. 6 (1996): 493–506. http://dx.doi.org/10.1006/lich.1996.0047.

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AbstractOver the last century, the distribution of Teloschistes flavicans has contracted from being widespread in the southern half of England and Wales to being limited to South-West England with outlying populations in Pembrokeshire and North Wales. Twelve core sites have been identified where the species is well established: ten of these are saxicolous/terricolous habitats on windy coastal cliff tops; the other two are lines of sycamore trees near the coast. At 39 further localities, some inland, the species is in very small amounts (often on one tree) and vulnerable to extinction. It is no

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12

CAVENDER, JAMES C., JOHN C. LANDOLT, EDUARDO M. VADELL, et al. "Distribution and ecology of dictyostelids in Madagascar." Phytotaxa 505, no. 2 (2021): 176–86. http://dx.doi.org/10.11646/phytotaxa.505.2.4.

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Samples for isolation of dictyostelid cellular slime molds were obtained from 20 collecting sites at 18 localities in south central and southeastern Madagascar during May 2009. At least thirty species of dictyostelids representing seven genera were recovered from 52 samples of soil/humus. This total included 17 species described as new to science, 13 species already known from various localities throughout the world, and four isolates that remain unidentified. Fourteen of the new species isolated from these samples are members of the whorl-branched, light-spored genus Heterostelium (formerly P

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13

Yatsyna, A. P. "Lichens genus Lepraria in Belarus: ecology and distribution of species." Proceedings of the National Academy of Sciences of Belarus, Biological Series 64, no. 1 (2019): 40–47. http://dx.doi.org/10.29235/1029-8940-2019-64-1-40-47.

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Sterile crustose lichens, i. e., those species that do not form fruiting bodies on the territory of Belarus, domestic scientists started to focus only at the beginning of the 21st century, despite the fact that already in the 60–70’s in the 20th century and methods for determining lichen substances in lichens were developed.Subjects of the study were herbarium specimens of lichenized fungi of the genus Lepraria in the amount of 68 herbarium bags from the collection of lichens MSK-L. As a result of the determination of secondary metabolites in the samples and the use of morphological features,

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14

Lushaj, B. M., S. Woodward, N. Keča, and M. Intini. "Distribution, ecology and host range of Armillaria species in Albania." Forest Pathology 40, no. 6 (2010): 485–99. http://dx.doi.org/10.1111/j.1439-0329.2009.00624.x.

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15

M. McPherson, Jana, and Walter Jetz. "Effects of species? ecology on the accuracy of distribution models." Ecography 30, no. 1 (2007): 135–51. http://dx.doi.org/10.1111/j.2006.0906-7590.04823.x.

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16

M. McPherson, Jana, and Walter Jetz. "Effects of species’ ecology on the accuracy of distribution models." Ecography 30, no. 1 (2007): 135–51. http://dx.doi.org/10.1111/j.0906-7590.2007.04823.x.

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17

Lock, Koen, Tim Adriaens, and Maarten Stevens. "Distribution and ecology of the Belgian Campodea species (Diplura: Campodeidae)." European Journal of Soil Biology 46, no. 1 (2010): 62–65. http://dx.doi.org/10.1016/j.ejsobi.2009.09.003.

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18

Bobrowski, Maria, Johannes Weidinger, Niels Schwab, and Udo Schickhoff. "Searching for ecology in species distribution models in the Himalayas." Ecological Modelling 458 (October 2021): 109693. http://dx.doi.org/10.1016/j.ecolmodel.2021.109693.

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19

Sinichkin, Evgeny Arkadyevich, Gennady Alekseevich Bogdanov, and Aleksandr Veniaminovich Dimitriev. "Ecology and distribution of rare lichens of the Chuvash Prisurye." Samara Journal of Science 9, no. 1 (2020): 92–100. http://dx.doi.org/10.17816/snv202091115.

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The paper contains data about 20 new and rare lichens of the Chuvash Prisurye. 10 lichens are new for the Chuvash Republic, 5 species are new for the Privolzhskaya Upland. The identified lichen species are indicators of old-growth, undisturbed and intact forests that have been preserved in specially protected natural areas. There are 18 species in the National Park Chuvash varmane and 8 species in the State Nature Reserve Prisursky. Geographical coordinates, distribution features in neighboring regions, ecological-substrate and phytocenotic confinement and age status are indicated for each spe

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20

Newbold, Tim. "Applications and limitations of museum data for conservation and ecology, with particular attention to species distribution models." Progress in Physical Geography: Earth and Environment 34, no. 1 (2010): 3–22. http://dx.doi.org/10.1177/0309133309355630.

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To conserve biodiversity, it is necessary to understand how species are distributed and which aspects of the environment determine distributions. In large parts of the world and for the majority of species, data describing distributions are very scarce. Museums, private collections and the historical literature offer a vast source of information on distributions. Records of the occurrence of species from these sources are increasingly being captured in electronic databases and made available over the internet. These records may be very valuable in conservation efforts. However, there are a num

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21

Bjelland, Torbjørg. "Comparative studies of the distribution and ecology of some oceanic species in the genus Leptogium (Lecanorales, Ascomycotina) in Norway." Nova Hedwigia 72, no. 1-2 (2001): 1–44. http://dx.doi.org/10.1127/nova.hedwigia/72/2001/1.

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22

Wittmann, Marion E., Matthew A. Barnes, Christopher L. Jerde, Lisa A. Jones, and David M. Lodge. "Confronting species distribution model predictions with species functional traits." Ecology and Evolution 6, no. 4 (2016): 873–79. http://dx.doi.org/10.1002/ece3.1898.

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23

Brummer, Alexander, and Erica Newman. "Derivations of the Core Functions of the Maximum Entropy Theory of Ecology." Entropy 21, no. 7 (2019): 712. http://dx.doi.org/10.3390/e21070712.

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The Maximum Entropy Theory of Ecology (METE), is a theoretical framework of macroecology that makes a variety of realistic ecological predictions about how species richness, abundance of species, metabolic rate distributions, and spatial aggregation of species interrelate in a given region. In the METE framework, “ecological state variables” (representing total area, total species richness, total abundance, and total metabolic energy) describe macroecological properties of an ecosystem. METE incorporates these state variables into constraints on underlying probability distributions. The method

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24

Hofner, Benjamin, Jörg Müller, and Torsten Hothorn. "Monotonicity-constrained species distribution models." Ecology 92, no. 10 (2011): 1895–901. http://dx.doi.org/10.1890/10-2276.1.

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25

Helmer, W., H. Strijbosch, and P. T. Scholte. "Distribution and ecology of lizards in the Greek province of Evros." Amphibia-Reptilia 10, no. 2 (1989): 151–74. http://dx.doi.org/10.1163/156853889x00188.

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AbstractDuring a field study in 1983-1984 in a 200 km 2 study area in the south of Evros province (Greece) the presence of 11 lizard species was established. For every species a distribution map within the area is supplied. In different parts of the area thc lizards formed different species combinations. Ophisops elegans appeared to vicariate in certain terrains with both Podarcis erhardii and P. taurica. By studying habitat selection and activity patterns of all species data on spatial and temporal niche segregation could be obtained. The activity patterns of all species were strongly influen

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26

Helaouët, Pierre, and Gregory Beaugrand. "Physiology, Ecological Niches and Species Distribution." Ecosystems 12, no. 8 (2009): 1235–45. http://dx.doi.org/10.1007/s10021-009-9261-5.

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27

Zurell, Damaris, Niklaus E. Zimmermann, Helge Gross, Andri Baltensweiler, Thomas Sattler, and Rafael O. Wüest. "Testing species assemblage predictions from stacked and joint species distribution models." Journal of Biogeography 47, no. 1 (2019): 101–13. http://dx.doi.org/10.1111/jbi.13608.

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28

Cassar, Thomas. "The praying mantises of the Maltese Islands: distribution and ecology (Mantodea)." Fragmenta Entomologica 52, no. 2 (2020): 341–48. http://dx.doi.org/10.4081/fe.2020.462.

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This study presents a species account of the mantises of the Maltese Islands, including notes on the ecology and distribution of each species. A total of three species are known to exist locally; Ameles spallanzania (Rossi, 1792), Mantis religiosa (Linnaeus, 1758) and Rivetina baetica Rambur, 1839. The presence of Ameles decolor (Charpentier, 1825) cannot be confirmed by any recently collected material, but the species is not excluded from the Maltese entomofauna. Two doubtful records are also discussed. All species present in the archipelago are typically found in Southern Europe and the Medi

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29

Mering, Sabine Von. "Tetronciumand its only species,T. magellanicum(Juncaginaceae): distribution, ecology and lectotypification." Willdenowia 43, no. 1 (2013): 13–24. http://dx.doi.org/10.3372/wi.43.43102.

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30

Guillaumin, J. J., Caroline Mohammed, N. Anselmi, et al. "Geographical distribution and ecology of the Armillaria species in western Europe." Forest Pathology 23, no. 6-7 (1993): 321–41. http://dx.doi.org/10.1111/j.1439-0329.1993.tb00814.x.

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31

Breckle, Siegmar W. "Distribution and ecology ofCystopteris (Athyriaceae) species within the Flora Iranica region." Plant Systematics and Evolution 155, no. 1-4 (1987): 59–65. http://dx.doi.org/10.1007/bf00936288.

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32

Ensikat, Hans-Jürgen, Hannah Wessely, Marianne Engeser, and Maximilian Weigend. "Distribution, Ecology, Chemistry and Toxicology of Plant Stinging Hairs." Toxins 13, no. 2 (2021): 141. http://dx.doi.org/10.3390/toxins13020141.

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Plant stinging hairs have fascinated humans for time immemorial. True stinging hairs are highly specialized plant structures that are able to inject a physiologically active liquid into the skin and can be differentiated from irritant hairs (causing mechanical damage only). Stinging hairs can be classified into two basic types: Urtica-type stinging hairs with the classical “hypodermic syringe” mechanism expelling only liquid, and Tragia-type stinging hairs expelling a liquid together with a sharp crystal. In total, there are some 650 plant species with stinging hairs across five remotely relat

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33

Doadrio, I., S. Perea, P. Garzón, J. L. González, V. C. Almada, and A. Pereira. "New distribution data on Spanish autochthonous species of freshwater fish." Graellsia 67, no. 1 (2011): 91–102. http://dx.doi.org/10.3989/graellsia.2011.v67.032.

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34

BÎRSAN, Cipran, Ana COJOCARIU, and Elena CENUŞĂ. "Distribution and Ecology of Clathrus archeri in Romania." Notulae Scientia Biologicae 6, no. 3 (2014): 288–91. http://dx.doi.org/10.15835/nsb639389.

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Although Clathrus archeri is a widely spread species in the Western Europe, in Romania it is considered a rare species, identified from only eight sites. In July 2013, it was found in two new sites from Gurghiu and Bârgău Mountains, in the Romanian Eastern Carpathians. This paper presents a detailed description of the new recorded specimens and of the habitat where this fungus was found. Plant communities where Clathrus archeri was recorded belong to the “mountain hay meadows” habitat type (Festuco rubrae - Agrostietum capillaris community). Taking into consideration the previous published dat

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35

Bely, Pavel, Vladimir Golubkov, Andrei Tsurykau, and Evgenii Sidorovich. "The Lichen Genus Cetrelia In Belarus: Distribution, Ecology And Conservation." Botanica Lithuanica 20, no. 2 (2015): 69–76. http://dx.doi.org/10.2478/botlit-2014-0010.

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AbstractTwo hundred and ten specimens of Cetrelia collected in Belarus in 1954-2012 were examined based on morphological and chemical characters. Three closely related species of Cetrelia (C. cetrarioides, C. monachorum and C. olivetorum) were identified in this study. The ecological notes and distribution maps of the detected species in Belarus were provided and their conservation status was discussed.

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36

VAUGHAN, I. P., and S. J. ORMEROD. "The continuing challenges of testing species distribution models." Journal of Applied Ecology 42, no. 4 (2005): 720–30. http://dx.doi.org/10.1111/j.1365-2664.2005.01052.x.

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37

van den BOOM, Pieter P. G., and John A. ELIX. "Notes on Halecania species, with descriptions of two new species from Asia." Lichenologist 37, no. 3 (2005): 237–46. http://dx.doi.org/10.1017/s0024282905014787.

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Two species of Halecania from Asia, H. lobulata van den Boom & Elix and H. pakistanica van den Boom & Elix are described as new to science. In addition, the new combination Halecania pepegospora (H. Magn.) van den Boom is made. The ecology, distribution and chemistry of some selected species are discussed and a key to the fifteen species known worldwide is given.

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38

Ricciardi, Anthony, and Henry M. Reiswig. "Freshwater sponges (Porifera, Spongillidae) of eastern Canada: taxonomy, distribution, and ecology." Canadian Journal of Zoology 71, no. 4 (1993): 665–82. http://dx.doi.org/10.1139/z93-091.

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During a recent survey of the freshwater sponges of eastern Canada (from Ontario to Newfoundland), 15 species were recorded, representing approximately 50% of the total number of species known from North America. Radiospongilla crateriformis, Spongilla aspinosa, and Trochospongilla horrida are reported from Canada for the first time. Two problematic species, Corvosporigilla novaeterrae and Spongilla johanseni, are reviewed and their status is revised. Detailed notes on taxonomy, morphology, distribution, and ecology are given. New limits of tolerance with respect to pH, water temperature, and

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39

Ramirez-Reyes, Carlos, Mona Nazeri, Garrett Street, D. Todd Jones-Farrand, Francisco J. Vilella, and Kristine O. Evans. "Embracing Ensemble Species Distribution Models to Inform At-Risk Species Status Assessments." Journal of Fish and Wildlife Management 12, no. 1 (2021): 98–111. http://dx.doi.org/10.3996/jfwm-20-072.

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Abstract Conservation planning depends on reliable information regarding the geographic distribution of species. However, our knowledge of species' distributions is often incomplete, especially when species are cryptic, difficult to survey, or rare. The use of species distribution models has increased in recent years and proven a valuable tool to evaluate habitat suitability for species. However, practitioners have yet to fully adopt the potential of species distribution models to inform conservation efforts for information-limited species. Here, we describe a species distribution modeling app

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40

Wendt, Lisiane Dilli, and Rosaly Ale-Rocha. "Geographic distribution of Epiplateinae Steyskal (Diptera: Richardiidae): New records and distribution maps." Check List 9, no. 5 (2013): 1091. http://dx.doi.org/10.15560/9.5.1091.

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Epiplateinae is a small subfamily of Richardiidae composed by three genera: Automola Loew, Epiplatea Loew and Omomyia Coquillett. Automola and Epiplatea have three and five valid species, respectively; both are widespread in the Neotropical Region. Omomyia has three valid species, which are restricted to arid areas of the southwestern United States. A list of all species of Epiplateinae, their previously known distribution and new records are provided. Material examined and maps with the geographic distribution of each species are also provided.

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41

Krebs, Charles J. "Whither mammalian ecology?" Journal of Mammalogy 101, no. 5 (2020): 1224–30. http://dx.doi.org/10.1093/jmammal/gyaa072.

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Abstract The critical agenda for mammalian ecologists over this century is to obtain a synthetic and predictive understanding of the factors that limit the distribution and abundance of mammals on Earth. During the last 100 years, a start has been made on this agenda, but only a start. Most mammal species have been described, but there still are tropical areas of undisclosed species richness. We have been measuring changes in distribution and abundance of many common mammals during the last century, and this monitoring agenda has become more critical as climate change has accelerated and habit

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42

TRẦN, HỮU ÐĂNG, HỒNG TRƯỜNG LƯU, NGỌC TOÀN TRẦN, THÀNH TRUNG NGUYỄN, QUỐC BÌNH NGUYỄN, and JANA LEONG-ŠKORNIČKOVÁ. "Three new Newmania species (Zingiberaceae: Zingibereae) from central Vietnam." Phytotaxa 367, no. 2 (2018): 145. http://dx.doi.org/10.11646/phytotaxa.367.2.4.

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Three new Newmania species, N. cristata, N. gracilis and N. sontraensis, are described here, bringing the number of species in this endemic Vietnamese genus to six. Descriptions, notes on ecology, phenology, distribution, preliminary IUCN assessments and colour plates are provided for each newly described species. An updated key to all six species and a map of their distributions are also given. We also report pseudovivipary in Newmania for the first time, namely in N. cristata.

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43

Marcer, Arnald, Llorenç Sáez, Roberto Molowny-Horas, Xavier Pons, and Joan Pino. "Using species distribution modelling to disentangle realised versus potential distributions for rare species conservation." Biological Conservation 166 (October 2013): 221–30. http://dx.doi.org/10.1016/j.biocon.2013.07.001.

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44

Holtan-Hartwig, J. "Two New Species of Peltigera." Lichenologist 20, no. 1 (1988): 11–17. http://dx.doi.org/10.1017/s0024282988000040.

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AbstractTwo new lichen species Peltigera frippii Holt.-Hartw. and P. scabrosella Holt.-Hartw.are described. Their morphology, chemistry, and ecology are discussed, and their distribution in Norway is mapped. New chemical data are also given for the related species P. lyngei Gyelnik, P. malacea (Ach.) Funck, P. neckeri Müll. Arg., and P. scabrosa Th. Fr.

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45

Andrus, Richard E. "Some aspects of Sphagnum ecology." Canadian Journal of Botany 64, no. 2 (1986): 416–26. http://dx.doi.org/10.1139/b86-057.

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Sphagnum species are ecologically prominent wetland plants with xerophytic adaptations and succession-directing acidification capabilities. Species are organized along environmental gradients of pH, cation concentrations, hummock and hollow, wet versus dry, shade versus sun, coastal versus inland, and cold versus warm. The known factors responsible for this organization include cation-exchange capacity, desiccation tolerance, desiccation resistance, water-holding capacity, drying rates, and photosynthetic response at differing water contents. Small-scale distribution of Sphagnum species can be

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46

Romanov, Roman E., and Sophia S. Barinova. "The Charophytes of Israel: historical and contemporary species richness, distribution, and ecology." Biodiversity: Research and Conservation 25, no. 1 (2012): 67–74. http://dx.doi.org/10.2478/v10119-012-0015-4.

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Abstract The historical and contemporary species richness, distribution, and ecology of Israel charophytes are described. The first charophyte collection in this region was made in the 19th century. Almost all reported localities were found earlier than 1970; some of them were not described. At the end of the 20th century, only two localities of two species were reported. According to the literature, 13 species, including two undetermined species of Chara, and nearly 23 exact localities are known from Northern and Central Israel. We found seven species and one variety of charophytes in 23 new

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47

Tremlová, Kateřina, and Zuzana Münzbergová. "IMPORTANCE OF SPECIES TRAITS FOR SPECIES DISTRIBUTION IN FRAGMENTED LANDSCAPES." Ecology 88, no. 4 (2007): 965–77. http://dx.doi.org/10.1890/06-0924.

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48

Liu, Chunlong, Christian Wolter, Weiwei Xian, and Jonathan M. Jeschke. "Species distribution models have limited spatial transferability for invasive species." Ecology Letters 23, no. 11 (2020): 1682–92. http://dx.doi.org/10.1111/ele.13577.

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49

Macalady, Jennifer L., Trinity L. Hamilton, Christen L. Grettenberger, Daniel S. Jones, Leah E. Tsao, and William D. Burgos. "Energy, ecology and the distribution of microbial life." Philosophical Transactions of the Royal Society B: Biological Sciences 368, no. 1622 (2013): 20120383. http://dx.doi.org/10.1098/rstb.2012.0383.

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Mechanisms that govern the coexistence of multiple biological species have been studied intensively by ecologists since the turn of the nineteenth century. Microbial ecologists in the meantime have faced many fundamental challenges, such as the lack of an ecologically coherent species definition, lack of adequate methods for evaluating population sizes and community composition in nature, and enormous taxonomic and functional diversity. The accessibility of powerful, culture-independent molecular microbiology methods offers an opportunity to close the gap between microbial science and the main

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50

Orsini, Vinícius Santana, André Valle Nunes, and Laura K. Marsh. "New distribution records of Pithecia rylandsi and Pithecia mittermeieri (Primates, Pitheciidae) and an updated distribution map." Check List 13, no. 3 (2017): 2123. http://dx.doi.org/10.15560/13.3.2123.

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New locations and extension of the known geographical distributions are reported for two recently-described species of saki monkeys: Pithecia rylandsi and Pithecia mittermeieri. The record of P. rylandsi confirms the presence of this species further south in the state of Mato Grosso, Brazil. The new record of P. mittermeieri, which occurred in an ecotone of Amazon, Cerrado, and Pantanal biomes, is the southernmost record for the genus. Recording the distribution extension of both species is essential for their conservation, as well as to promote more studies about their ecology, behaviour, and

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