Influence of irregular shelterwood treatments on intensity and severity after a large wildfire in lodgepole pine stands: A case study from the interior British Columbia.

Climate change has significantly impacted the wildfire regimes in lodgepole pine forests, resulting in prolonged fire seasons and altered fire behaviour. In North America, fire patterns have shifted towards more frequent and severe wildfires after a century of fire suppression. In response, silviculture practices in fire-prone areas should aim to restore diverse forest structures that are resistant or resilient to wildfires.

Continental-scale tree-ring-based projection of Douglas-fir growth: Testing the limits of space-for-time substitution.

A central challenge in global change research is the projection of the future behavior of a system based upon past observations. Tree-ring data have been used increasingly over the last decade to project tree growth and forest ecosystem vulnerability under future climate conditions. But how can the response of tree growth to past climate variation predict the future, when the future does not look like the past? Space-for-time substitution (SFTS) is one way to overcome the problem of extrapolation: the response at a given location in a warmer future is assumed to follow the response at a warmer location today.

Synthesis and Isomeric Analysis of Ru Complexes Bearing Pentadentate Scaffolds.

A Ru-pentadentate polypyridyl complex [Ru(κ-N-bpy2PYMe)Cl] (1, bpy2PYMe = 1-(2-pyridyl)-1,1-bis(6-2,2'-bipyridyl)ethane) and its aqua derivative [Ru(κ-N-bpy2PYMe)(HO)] (2) were synthesized and characterized by experimental and computational methods. In MeOH, 1 exists as two isomers in different proportions, cis (70%) and trans (30%), which are interconverted under thermal and photochemical conditions by a sequence of processes: chlorido decoordination, decoordination/recoordination of a pyridyl group, and chlorido recoordination. Under oxidative conditions in dichloromethane, trans-1 generates a [Ru(κ-N-bpy2PYMe)Cl] intermediate after the exchange of a pyridyl ligand by a Cl counterion, which explains the trans/cis isomerization observed when the system is taken back to Ru(II).

Synthesis and Characterization of a Tetrapodal NO4(4-) Ligand and Its Transition Metal Complexes.

We present the synthesis and characterization of alkali metal salts of the new tetraanionic, tetrapodal ligand 2,2'-(pyridine-2,6-diyl)bis(2-methylmalonate) (A4[PY(CO2)4], A = Li(+), Na(+), K(+), and Cs(+)), via deprotection of the neutral tetrapodal ligand tetraethyl 2,2'-(pyridine-2,6-diyl)bis(2-methylmalonate) (PY(CO2Et)4). The [PY(CO2)4](4-) ligand is composed of an axial pyridine and four equatorial carboxylate groups and must be kept at or below 0 °C to prevent decomposition. Exposing it to a number of divalent first-row transition metals cleanly forms complexes to give the series K2[(PY(CO2)4)M(H2O)] (M = Mn(2+), Fe(2+), Co(2+), Ni(2+), Zn(2+)).

A new direction in dye-sensitized solar cells redox mediator development: in situ fine-tuning of the cobalt(II)/(III) redox potential through Lewis base interactions.

Dye-sensitized solar cells (DSCs) are an attractive renewable energy technology currently under intense investigation. In recent years, one area of major interest has been the exploration of alternatives to the classical iodide/triiodide redox shuttle, with particular attention focused on cobalt complexes with the general formula [Co(L)(n)](2+/3+). We introduce a new approach to designing redox mediators that involves the application of [Co(PY5Me(2))(MeCN)](2+/3+) complexes, where PY5Me(2) is the pentadentate ligand, 2,6-bis(1,1-bis(2-pyridyl)ethyl)pyridine.