tree hollows
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Author(s):  
Cara E. Penton ◽  
Ian J. Radford ◽  
Leigh-Ann Woolley ◽  
Brenton von Takach ◽  
Brett P. Murphy

Insects ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 465
Author(s):  
Ondřej Machač ◽  
Ivan Hadrián Tuf

Spiders are common inhabitants of tree hollows, as well as bird nesting boxes, especially in autumn and winter. Some species of spiders use bird nesting boxes for overwintering. We investigated spider assemblages in nesting boxes and how temperature influences the abundance of overwintering spiders in nesting boxes in lowland forest in the Czech Republic. The study was conducted in the European winters of 2015–2017. In total, 3511 spider specimens belonging to 16 identified species were collected from nesting boxes over three years in late autumn and winter. Almost all species were arboreal specialists. The dominant species were Clubiona pallidula, Anyphaena accentuata, Platnickina tincta, and Steatoda bipunctata. Although the tree species had no effect on the abundance of overwintering spiders, the presence of nest material affected the abundance of spiders in the nesting boxes (preferred by C. pallidula and P. tincta). In general, spiders resettled nesting boxes during winter only sporadically, however A. accentuata reoccupied boxes continuously, and its activity was positively correlated with the outside temperature. Nesting boxes support insect-eaters all year around—birds during spring and summer and spiders during autumn and winter.


Author(s):  
Jesús Hernández‐Corral ◽  
Alejandra García‐López ◽  
Miguel Ángel Ferrández ◽  
Estefanía Micó

2021 ◽  
pp. 109-150
Author(s):  
Mike Hodda ◽  
Walter Traunspurger

Abstract This chapter discusses the ecology and biogeography of nematodes from freshwater environments that are extreme in temperature, chemical composition, variability, or isolation. Described and compared are the compositions of nematode faunas from hot or mineral springs, pools and bogs in polar regions, intermittent lakes or pools or streams, freshwater pools in bromeliads or tree hollows, stemflow, fresh groundwaters, and caves. Comparisons of the nematode faunas from these extreme habitats with those from more typical freshwater environments are also provided. Also discussed are nematodes with evolutionary affinities to freshwaters that are found in estuarine sediments along with nematodes from freshwaters with evolutionary affinities to otherwise marine taxa. The emphasis is on broad ecological patterns rather than on detailed species interactions with the various freshwater environments. Thus, the chapter focuses on genera or higher taxa rather than species.


2021 ◽  
Vol 38 ◽  
pp. 13-18
Author(s):  
David Young ◽  
◽  
Phil Bell ◽  
Nick Mooney ◽  
◽  
...  

Roost-sites and roosting behaviour are described for a juvenile female, an adult female and an adult male Tasmanian Masked Owl Tyto novaehollandiae castanops in a forest–farmland landscape. The two female Owls were radiotracked, and frequently used roost-sites in the core area of use. Roost-sites were typically associated with small watercourses, on the edges of large contiguous forest patches within a complex mosaic of forest and pasture. The juvenile Owl used many different vegetation roost-sites after dispersing from her presumed natal territory. In contrast, the adult female used few roosts, including two vegetation roosts and one tree-hollow, and only one roost (a tree-hollow) was located for the adult male. The primary tree-hollow roost-sites of the male and female Owls were <400 m apart and were both <1200 m from a suspected nest-tree. This strongly suggests that the spatial proximity of nest- and roost-sites may be critical to facilitate territorial, foraging and reproductive behaviours of breeding pairs. Increased knowledge of spatial ecology and utilisation of tree-hollows by adult Tasmanian Masked Owls is crucial for their conservation.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Reannan Honey ◽  
Chris McLean ◽  
Brad R Murray ◽  
Jonathan K Webb

Abstract In urban bushland, the installation of nest boxes is widely used to compensate for the loss of natural tree hollows. However, current nest box designs may not provide thermal refuges for wildlife during summer heatwaves, particularly if internal temperatures exceed the upper critical temperatures of wildlife. We investigated whether the addition of roofing insulation to nest boxes deployed for sugar gliders (Petaurus breviceps) and squirrel gliders (Petaurus norfolcensis) in urban bushland would reduce internal nest box temperatures during summer heatwaves. We measured temperatures of 44 insulated and 47 uninsulated nest boxes during one of the hottest summers on record (2018–2019) in the Lake Macquarie region of NSW, Australia, a period during which several prolonged heatwaves occurred. Over the 90-day study, maximum temperatures were, on average, 3.1°C lower in insulated boxes than in uninsulated boxes. The addition of insulation significantly lowered nest box temperatures regardless of aspect (north or south facing) or day of measurement. Temperatures exceeded the upper critical temperature (35.1°C) of gliders more frequently in uninsulated nest boxes (28% of days) than in insulated nest boxes (8% days). Although the addition of insulation to nest boxes lowered their internal temperatures, during heatwaves spanning 23 days, nest box temperatures exceeded the upper critical temperatures of gliders on 58% and 23% of days in uninsulated and insulated nest boxes respectively. These findings underscore the importance of retaining natural hollows in urban bushland to provide thermally suitable refuges for wildlife during extreme heat events.


Zootaxa ◽  
2020 ◽  
Vol 4885 (3) ◽  
pp. 384-394
Author(s):  
ANATOLY BOBROV ◽  
YURI MAZEI

New species, Frenopyxis stierlitzi, is described from tree hollows in the urban parks in Moscow (Russia) and Potsdam (Germany). The species belongs to the new genus of the family Centropyxidae and characterized by unique character, i.e. an internal thick organic lip surrounding an aperture and continuing in a bridle, which connects an aperture with the internal side of a shell wall and broaden in the place of connection of a bridle and a shell wall. The systematics of the family Centropyxidae is discussed and the importance of the structures, which divide inner shell volume into compartments, is underlined. 


PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e10243
Author(s):  
Zhengya Jin ◽  
Jian Chen ◽  
Xiujun Wen ◽  
Cai Wang

Formosan subterranean termites, Coptotermes formosanus Shiraki, usually transport clay materials into tree hollows and bait stations. Our previous research showed that C. formosanus preferred to aggregate in the locations containing field-collected clay samples, but it was not clear whether this preference was influenced by clay types and/or moisture. In the present study, we conducted multiple-choice tests under low-moisture (25% moisture) or moderate-moisture (50% moisture) conditions to evaluate the aggregation and wood-feeding preferences of C. formosanus responding to hollow wooden cylinders (simulation of tree hollows) or baiting containers (simulation of bait stations) filled with different clay materials (bentonite , kaolin, chlorite, illite, or attapulgite), soil, or unfilled. Under low-moisture conditions, the majority of termites were found in the wooden cylinders or baiting containers filled with bentonite. Under moderate-moisture conditions, however, termites preferred to aggregate in wooden cylinders filled with chlorite or attapulgite; the percentages of termites that stayed in baiting containers filled with chlorite, attapulgite or soil were similar, which were significantly higher than those that filled with kaolin, illite, or unfilled. We then conducted no-choice tests to study the effect of clay materials on termites. Under low-moisture conditions, clay filled in the baiting containers significantly increased survivorship and body water percentage (an indicator of termite vigor) of termites, whereas no similar effect was detected under moderate-moisture conditions. This study demonstrated that both clay type and moisture affect termites’ preference.


2020 ◽  
Vol 57 (10) ◽  
pp. 1891-1901
Author(s):  
Andrew M. Rogers ◽  
Andrea S. Griffin ◽  
Berndt J. Rensburg ◽  
Salit Kark

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