No abstract

The timing of many biological events, including butterfly imago emergence, has advanced under climate change, with the rate of these phenological changes often differing among taxonomic groups. Such inter-taxa variability can lead to phenological mismatches. For example, the timing of a butterfly's flight period may become misaligned with a key nectar resource, potentially increasing the extinction risk to both species. Here we fit statistical models to field data to determine how the phenology of the marbled white butterfly, Melanargia galathea, and its main nectar source, greater knapweed, Centaurea scabiosa, have changed over recent years at three sites across the UK. We also consider whether topographical diversity affects C. scabiosa's flowering period. At our focal site, on the species northern range limit, we find that over a 13year period the onset of C. scabiosa's flowering period has become later whilst there is no obvious trend over time in the onset of M. galathea's flight period. In recent years, butterflies have started to emerge before their key nectar source was available across most of the site. This raises the intriguing possibility that phenological mismatch could be an unrecognised determinant of range limits for some species. However, the presence of topographical diversity within the site decreased the chance of a mismatch occurring by increasing the length of the flowering period by up to 14 days. We suggest that topographical diversity could be an important component in minimising phenological mismatches under future climate change.

Results indicate that sex differences exist in motor, but not sensory, components of the startle reflex. Findings also reveal that administration of 0.45 mg/kg dexamphetamine to healthy humans does not mimic PPI effects observed in schizophrenia.

Raccoons (Procyon lotor) often are considered a nuisance species in suburban and urban areas, and thus, must be removed. However, raccoons are capable of removing bait from cage traps without being captured and appear to avoid baits that are infested with fire ants (Solenopsis invicta). We modified Tomahawk• cage traps with an extended metal floor that acted as a trip device, hardware cloth wrapped around the back half of traps to reduce the potential of raccoons obtaining bait without entering the traps, and developed a hook upon which to place baits to minimize the probability of fire ants locating the bait. We then compared the proportion of raccoon captures, baits missing, and baits with fire ants between cage traps with and without the modified floor and bait hook. Twenty-five raccoons were caught, 80 baits were stolen, and 108 baits were infested with fire ants during 432 trap-nights. A greater proportion of raccoons were caught in (G=ll.7, 3 df, P < 0.01) and fewer baits were stolen from (G=ll.O, 3 df, P < 0.02) cage traps modified with the extended metal floor than without the modification. Traps equipped with hooks were minimally affected by fire ants present on the baits (i.e., 8 of216 baits; 3.7%), which was much less (G=59.0, 1 df, P < 0.0001) than traps without bait hooks (46.3%). Our modifications to cage traps enhanced the capture success of raccoons and should be considered if live-trapping of raccoons is required, especially in areas where fire ants are problematic.