SUMMARYSeasonal and circadian rhythms control fundamental physiological processes including neural excitability and synaptic plasticity that can lead to the periodic modulation of motor behaviors like social vocalizations. Parental male midshipman fish produce three call types during the breeding season: long duration (min to >1 h) advertisement 'hums', frequency and amplitude modulated agonistic 'growls' (s), and very brief (ms) agonistic 'grunts' produced either singly or repetitively as 'grunt trains' for up to several minutes. Fictive grunts that establish the temporal properties of natural grunts are readily evoked and recorded in vivo from vocal occipital nerve roots at any time of day or year by electrical microstimulation in either the midbrain periaqueductal gray or a hindbrain vocal pre-pacemaker nucleus. Now, as shown here, the longer duration fictive growls and hums can also be elicited, but are restricted to the nocturnal reproductive season. A significant drop in call threshold accompanies the fictive growls and hums that are distinguished by their much longer duration and lower and more regular firing frequency. Lastly, the long duration fictive calls are dependent upon increased stimulation time and intensity and hence may result from activitydependent changes in the vocal motor circuit that are themselves modulated by seasonal and circadian rhythms.

Plants and mycorrhizal fungi influence each other’s abundance, diversity, and distribution. How other biotic interactions affect the mycorrhizal symbiosis is less well understood. Likewise, we know little about the effects of climate change on the fungal component of the symbiosis or its function. We synthesized our long-term studies on the influence of plant parasites, insect herbivores, competing trees, and drought on the ectomycorrhizal fungal communities associated with a foundation tree species of the southwestern United States, pinyon pine (Pinus edulis), and described how these changes feed back to affect host plant performance. We found that drought and all three of the biotic interactions studied resulted in similar shifts in ectomycorrhizal fungal community composition, demonstrating a convergence of the community towards dominance by a few closely related fungal taxa. Ectomycorrhizal fungi responded similarly to each of these stressors resulting in a predictable trajectory of community disassembly, consistent with ecological theory. Although we predicted that the fungal communities associated with trees stressed by drought, herbivory, competition, and parasitism would be poor mutualists, we found the opposite pattern in field studies. Our results suggest that climate change and the increased importance of herbivores, competitors, and parasites that can be associated with it, may ultimately lead to reductions in ectomycorrhizal fungal diversity, but that the remaining fungal community may be beneficial to host trees under the current climate and the warmer, drier climate predicted for the future.