We examined whether pinyon mice ( Peromyscus truei) and brush mice ( P. boylii) could act as directed dispersal agents of pinyon pine ( Pinus edulis) through differential responses to soil particle size and rock cover. In field experiments, we allowed mice to either cache pinyon seeds or recover artificially cached seeds (pilfer) from quadrats containing large- or small-particle soils. Both species placed most (70%) seed caches in small-particle soil. Pilfering was the same from both particle sizes in the first year, while more seeds were pilfered from large-particle soils in the second year. In separate experiments, rock cover interacted with soil particle size, with both species placing over 50% of their caches in small-particle soil with rock cover. Overall, we found greater seed-caching in small-particle soils near rocks, with equal or lower pilfering from small-particle soils, suggesting more seeds would survive in small-particle soils near rock cover. Three lines of evidence supported the hypothesis that mice could act as directed dispersers by moving pinyon seeds to beneficial microsites for germination and establishment. First, in greenhouse experiments, pinyon seed germination was 4 times greater in small-particle soil cores than in large-particle soil cores. Second, soils near rocks had significantly higher water content than areas of open soil at the driest time of the year, a critical factor for seedling survival in the arid southwestern USA. Third, 75% of juvenile pinyon trees were growing in small-particle soils, and 45% were growing near rock nurses.
We used maps of fire evidence, fire scar dendrochronology, forest age-structure analysis, and landscape analysis to investigate fire history at pinyon pine ( Pinus edulis Engelm.) – juniper ( Juniperus osteosperma (Torr.) Little, Juniperus scopulorum Sarg.) woodland – ponderosa pine ( Pinus ponderosa P. & C. Lawson) forest ecotones in Arizona (Tusayan) and in New Mexico (Canjilon). Results showed that charred trees were not evenly distributed across vegetative communities but were significantly (p < 0.001) more abundant than expected in ponderosa pine communities. Composite fire scar analysis indicated that surface fires occurred in ponderosa pine stands at both sites and burned at intervals of 7.2–11.1 years (WMPI; Weibull median probability interval). At Tusayan, landscape structure was fine grained, and maximum pinyon age was >200 years across 80% of the site. At Canjilon, landscape pattern was relatively coarse, and most pinyon patches were 200–300 years old. Cumulative standing age distributions suggested pinyon–juniper fire rotations of 340 and 290 years at Tusayan and Canjilon, respectively. We concluded the following: (i) surface fires in ponderosa pine stands did not spread through pinyon–juniper communities at either site, (ii) fire evidence was prevalent across both sites, but old pinyon trees indicated that no widespread lethal fires had occurred in the last 300–400 years, and (iii) structurally heterogeneous landscapes suggested that historical pinyon–juniper fires were of limited extent but lethal in patches.
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