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  1. The timing of life events (phenology) can be influenced by climate. Studies from around the world tell us that climate cues and species' responses can vary greatly. If variation in climate effects on phenology is strong within a single ecosystem, climate change could lead to ecological disruption, but detailed data from diverse taxa within a single ecosystem are rare. We collated first sighting and median activity within a high-elevation environment for plants, insects, birds, mammals and an amphibian across 45 years (1975–2020). We related 10 812 phenological events to climate data to determine the relative importance of climate effects on species’ phenologies. We demonstrate significant variation in climate-phenology linkage across taxa in a single ecosystem. Both current and prior climate predicted changes in phenology. Taxa responded to some cues similarly, such as snowmelt date and spring temperatures; other cues affected phenology differently. For example, prior summer precipitation had no effect on most plants, delayed first activity of some insects, but advanced activity of the amphibian, some mammals, and birds. Comparing phenological responses of taxa at a single location, we find that important cues often differ among taxa, suggesting that changes to climate may disrupt synchrony of timing among taxa. 
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  2. Abstract

    Floral microbes, including bacteria and fungi, alter nectar quality, thus changing pollinator visitation. Conversely, pollinator visitation can change the floral microbial community.

    Most studies on dispersal of floral microbes have focused on bees, ants or hummingbirds, yet Lepidoptera are important pollinators.

    We asked (a) where are microbes present on the butterfly body, (b) do butterflies transfer microbes while foraging, and (c) how does butterfly foraging affect microbial abundance on different floret structures.

    The tarsi and proboscis had significantly more microbes than the thorax in wild‐caughtGlaucopsyche lygdamus(Lepidoptera: Lycaenidae) andSpeyeria mormonia(Lepidoptera: Nymphalidae).Glaucopsyche lygdamus, a smaller‐bodied species, had fewer microbes thanS. mormonia.

    As a marker for microbes, we used a bacterium (Rhodococcus fascians,near NCBI Y11196) isolated from aS. mormoniathat was foraging for nectar, and examined its dispersal byG. lygdamusandS. mormoniavisiting florets ofPyrrocoma crocea(Asteraceae). Microbial dispersal among florets correlated positively with bacterial abundance in the donor floret. Dispersal also depended on butterfly species, age, and bacterial load carried by the butterfly.

    Recipient florets had less bacteria than donor florets. The nectaries had more bacteria than the anthers or the stigmas, while anthers and stigmas did not differ from each other. There was no differential transmission among floral organs.

    Lepidoptera thus act as vectors of floral microbes. Including Lepidoptera is thus crucial to an understanding of plant–pollinator–microbe interactions. Future studies should consider the role of vectored microbes in lepidopteran ecology and fitness.

     
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  3. Abstract

    Stressful juvenile developmental conditions can affect performance and fitness later in life. In holometabolous insects such as butterflies, development under stressful conditions may lead to smaller adult size, lower reproductive output, and shorter lifespan. However, how larval developmental stress affects energy intake and expenditure in adult individuals is poorly understood.

    We subjected last‐instar larvae ofSpeyeria mormoniaEdwards (Lepidoptera: Nymphalidae) to periodic dietary restriction (DR) to examine the allocation of energy and nutrients among different life history processes. We measured adult food intake, resting metabolic rate (RMR), metabolic flight capacity, lifespan, and reproductive output. Consistent with pressure to disperse from a poor environment while maintaining offspring number, we predicted that stressed individuals would have increased adult food intake and higher flight capacity.

    Adult body size was strongly reduced. Contrary to predictions, we found no compensatory adult feeding. Mass‐adjusted flight metabolic rate was reduced, suggesting poor dispersal capacity. Larval DR did not affect adult lifespan, nor did the rate of metabolic senescence change. Larval DR did affect RMR, as stressed females had a steeper slope between RMR and body mass, which may reflect differences in physiological activity due to condition.

    Fecundity decreased less than predicted based on body mass. Instead of investing in flight capacity, females increased relative allocation to reproduction, which may partly buffer against poor environmental conditions.

    Understanding the interplay of energy acquisition and allocation to life history traits across the life cycle is vital for predicting responses to environmental change.

     
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  4. Abstract

    Rapid environmental change can decouple previously reliable cues from important resources, causing specialized recognition systems to result in maladaptive behaviors. For native herbivorous insects, such evolutionary traps are often imposed by attractive invasive plants that prove harmful to their offspring. Despite the costs of ovipositing on a poor‐quality host, evolutionary traps are expected to persist when overlapping cue sets (cue similarity) link decreased preference for the novel, unsuitable plant with decreased preference for the historical or native resource. We evaluated the role of cue similarity in the persistence of maladaptive oviposition by a native butterfly on a lethal, invasive mustard. While the novel plant shares glucosinolate cues with at least one of the native hosts and the most abundant cue is a strong oviposition stimulant, we found that this cue was not a major driver of preference for either plant. Nor was preference for the two plants correlated, meaning decreased preference for the invasive mustard would not cause butterflies to miss potential oviposition opportunities on the superior native host. Instead, butterfly preference was modified by previous experience in a way that suggests that frequent encounters with native hosts in the wild may buffer butterflies against this evolutionary trap.

     
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  5. Abstract

    Evolutionary traps arise when organisms use novel, low‐quality or even lethal resources based on previously reliable cues. Persistence of such maladaptive interactions depends not only on how individuals locate important resources, such as host plants, but also the mechanisms underlying poor performance.Pieris macdunnoughii(Remington) (Lepidoptera: Pieridae) lays eggs on a non‐native mustard,Thlaspi arvense(L.) (Brassicaceae), which is lethal to the larvae. We first tested whether larval feeding behavior was affected before (pre‐) ingestion or following (post‐) ingestion of leaf material, indicating activity of feeding deterrents, toxins, or both in this evolutionary trap. Neonates were less likely to start feeding and eventually fed more slowly onT. arvensethan on the native host plantCardamine cordifolia(Gray) (Brassicaceae) in both laboratory and field. Starvation was a primary cause of mortality, indicating the role of a feeding deterrent. Feeding did not differ between larvae from invaded and uninvaded population. Second,T. arvensedefensive chemistry is dominated by the glucosinolate sinigrin (allyl or 2‐propenyl glucosinolate). Adding sinigrin to the leaves ofT. arvenseand native hostsC. cordifoliaandDescurainia incana(Bernhardi ex Fischer & Meyer) (Brassicaceae) delayed the onset of feeding, caused larvae to feed more slowly, and decreased survival on the native hosts. This evolutionary trap may not be driven by a novel deterrent, but rather by a change in the concentration of a deterrent found in native hosts. Many insects have adapted to evolutionary traps posed by invasive plants, incorporating the new plant into their diets.Thlaspi arvenseremains lethal toP. macdunnoughii, and pre‐ingestive deterrents such as excess sinigrin may contribute to persistent maladaptation.

     
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