Long-term trends, total numbers and species richness of increasing waterbird populations at sites on the edge of their winter range: cold-weather refuge sites are more important than protected sites

2015 ◽  
Vol 156 (4) ◽  
pp. 923-932 ◽  
Author(s):  
Zuzana Musilová ◽  
Petr Musil ◽  
Jan Zouhar ◽  
Dušan Romportl
Author(s):  
Shaun Lovejoy

“Expect the cold weather to continue for the next ten days, followed by a warm spell.” This might have been the fourteen- day weather forecast for Montreal on December, 31, 2006 (Fig. 5.1, top). But imagine what it might have been if Earth rotated about its axis ten times more slowly, so that the length of the day coincided with the ten- day weather– macroweather transition scale— an alignment of scales almost achieved on Mars. In that case (Fig. 5.1, bottom) we would have heard, “Expect mild weather on Monday, followed by freezing temperatures, until a warm spell on Thursday, followed by a brisk Friday and Saturday, a warming on Sunday and Monday, followed by freezing on Tuesday, then a four- day warm period followed by freezing and then warming.” Although long- term trends in weather can persist for up to ten days or so, in macroweather, the upshifts tend to be followed immediately by downshifts (and vice versa) and, although longer term trends exist, they are much more subtle, resulting from imperfect cancelations of successive fluctuations. The tendency of macroweather fluctuations to cancel rather than to accu­mulate is its defining feature, and cancelation is synonymous with stability. Quantitatively, it implies that the temporal fluctuation exponent H is negative. In the weather regime with positive H, the temperature, wind, and other variables wander up and down with prolonged swings. The weather is a meta­phor for instability. If we average macroweather over longer and longer times, its variability is reduced systematically so that it appears to converge to a well-defined value. In that sense, macroweather is what you expect, the weather is what you get. But what about macroweather’s spatial properties? As usual, forecasts can be explained with recourse to maps. For example, Plate 5.1 (left) shows the day- to-day evolution of the daily temperatures corresponding to the forecast in Figure 5.1 (top).


2015 ◽  
Vol 21 (7) ◽  
pp. 792-802 ◽  
Author(s):  
Anne Eskildsen ◽  
Luísa G. Carvalheiro ◽  
W. Daniel Kissling ◽  
Jacobus C. Biesmeijer ◽  
Oliver Schweiger ◽  
...  

2006 ◽  
Vol 17 (3) ◽  
pp. 316-334 ◽  
Author(s):  
David W. Steadman ◽  
Sharyn Jones

AbstractWe compare the bone assemblages of Milford 1 (TOB-3) and Golden Grove (TOB-13) in Tobago, West Indies. Milford 1 is a small preceramic occupation (ca. 3000-2800 cal B.P.), whereas Golden Grove is a large ceramic-period village (ca. 1700-900 cal B.P.). Species richness at TOB-13 is greater than at TOB-3, both in marine (67 vs. 39 fishes) and terrestrial (32 vs. 9) taxa. Major shifts in marine exploitation from the preceramic to ceramic periods can be seen in relative abundance of tuna, toadfishes, and in fishes inhabiting mangrove and brackish water environments, and decreases in relative abundance of parrotfish, carnivorous reef fishes, and sea turtles. The abundance of tuna bones at TOB-13 is uniquely high among West Indian archaeological sites. For terrestrial taxa, the difference in species richness exceeds the expected, including decreased specialization on big game (peccaries) at TOB-13, with a greater tendency to hunt reptiles, birds, and mammals of all sizes at TOB-3. Factors underlying the shifts in fishing and hunting may include different collection methods and food preferences of non-Arawakan (preceramic) vs. Arawakan (ceramic) peoples, as well as human-induced declines in populations of peccaries, sea turtles, and selected fish species. Another possible factor is site setting, with the inhabitants of TOB-13 having enhanced access to mangrove habitats.


Parasitology ◽  
2020 ◽  
pp. 1-13
Author(s):  
Jerzy M. Behnke ◽  
Michael T. Rogan ◽  
Philip S. Craig ◽  
Joseph A. Jackson ◽  
Geoff Hide

Abstract Helminth infections in wood mice (n = 483), trapped over a period of 26 years in the woods surrounding Malham Tarn in North Yorkshire, were analysed. Although 10 species of helminths were identified, the overall mean species richness was 1.01 species/mouse indicating that the helminth community was relatively depauperate in this wood mouse population. The dominant species was Heligmosomoides polygyrus, the prevalence (64.6%) and abundance (10.4 worms/mouse) of which declined significantly over the study period. Because of the dominance of this species, analyses of higher taxa (combined helminths and combined nematodes) also revealed significantly declining values for prevalence, although not abundance. Helminth species richness (HSR) and Brillouin's index of diversity (BID) did not show covariance with year, neither did those remaining species whose overall prevalence exceeded 5% (Syphacia stroma, Aonchotheca murissylvatici and Plagiorchis muris). Significant age effects were detected for the prevalence and abundance of all higher taxa, H. polygyrus and P. muris, and for HSR and BID, reflecting the accumulation of helminths with increasing host age. Only two cases of sex bias were found; male bias in abundance of P. muris and combined Digenea. We discuss the significance of these results and hypothesize about the underlying causes.


1987 ◽  
Vol 65 (4) ◽  
pp. 981-986 ◽  
Author(s):  
Uldis Roze

Long-term radiotelemetry was used to study patterns of den use and winter movement in porcupines (Erethizon dorsatum) in New York. Six of eight animals used dens regularly; the rest spent most of their winters in the shelter of hemlock stands (Tsuga canadensis). Animals entered dens in October–November after minimum daily temperatures had fallen below 0 °C for 6.8 days. Before this period, animals used temporary dens in response to rain or cold weather. Dens were abandoned in April when minimum daily temperatures rose above 0 °C and snow cover melted. Animals that left dens early typically sought the shelter of hemlock stands. Animals changed dens, on average, every 23 days. A single den-using adult male changed dens every 9.3 days. Den change was stimulated by disturbance. Animals showed strong year to year den fidelity. Animals shared dens 12% of the time. In all cases where sharing animals could be identified, they constituted a male–female pair that had previously shared a summer territory. Animals denned only in ready-made cavities such as rock outcrops, live hollow trees, outbuildings, and hollow logs. Heat-conserving features of such dens and of hemlock shelters are discussed. For three of four winters of the study, winter range averaged 7.4 ha, 11.4% of the nonwinter range. During the fourth winter, when snowfall was only 40% of normal, winter range did not differ significantly from nonwinter range.


2017 ◽  
Vol 20 (9) ◽  
pp. 1148-1157 ◽  
Author(s):  
Ryan D. Batt ◽  
James W. Morley ◽  
Rebecca L. Selden ◽  
Morgan W. Tingley ◽  
Malin L. Pinsky

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