Alternatives to Lotka-Volterra competition: Models of intermediate complexity

A family of one-level differential-equation competition models in which two populations are limited by the energy flowing into the system generates the following results. For competitors on the same and only resource: 1) Purely exploitative competition leads to exclusion; which species wins depends on relative abilities to appropriate and extract energy from the resource, and the relative death and maintenance rates. 2) If conspecific interference (e.g., deaths or energy loss from fighting, cannibalism, or display) is sufficiently high relative to abilities to exploit the common resource, competition for the same resource can lead to coexistence. 3) If heterospecific interference is sufficiently high relative to abilities to exploit the common resource, competition for the same resource can lead to a priority effect, in which the outcome depends on initial population sizes. 4) Depending on whether situation (2) or (3) prevails, an increase in the amount of the common resource can convert an outcome in which one species always wins into one giving coexistence (2) or a priority effect (3). 5) If species are similar to one another in their abilities to appropriate and extract energy from the common resource and show reciprocity in intererence costs, competition can have multiple outcomes; either one species wins or the species coexist, depending on initial values.For competition on the same resource, but with each species monopolizing an exclusive resource as well: 1) Purely exploitative competition always leads to a unique point coexistence. 2) If interference is added to the system described in (1), two points of coexistence, separated by a saddle (an “unstable equilibrium”) are possible. This is favored by a) a small yield from the exclusive resources relative to the common one; and b) strong interspecific relative to intraspecific interference.     

Observations on the central mechanism of acetylsalicylate antipyresis.

Leukocytic pyrogen and sodium acetylsalicylate (ASA) were microinjected into the anterior hypothalamus (AH) of urethane anesthetized cats under thermoneutral conditions. The responses of single, identified thermoregulatory neurons in the AH to leukocytic pyrogen placed in the contralateral AH were examined initially. The attempt was then made to determine the effect of ASA on the activity of pyrogen challenged neurons when injected into the AH area opposite to that which received the pyrogen. Stereotaxically located AH units were defined as thermoregulatory by their response to body surface and hypothalamic thermal stimulation; both “thermopositive” (warm) and “thermonegative” (cold) types were studied. Administration of the leukocytic pyrogen was always followed by a change in the discharge rate of the distal thermoregulatory neurons. About half of the units were excited and half were depressed regardless of their thermoresponsive behavior. When ASA was injected after the pyrogen into the opposite AH area, it always altered the neuronal activity and the change was invariably in the direction of the unit's thermal response. The findings indicate that the antipyresis produced by ASA is not due to competition with leukocytic pyrogen for a common receptor site.     

Effect of immersion in seawater on egg survival in the lizard<Emphasis Type="Italic"> Anolis sagrei</Emphasis>

Studies on the lizard, Anolis sagrei, revealed that after Hurricane Floyd devastated the Bahamas in 1999, some populations consisted only of hatchlings. Because the storm surge of the hurricane completely inundated these islands, apparently for up to 6 h, survival of anole eggs in salt water for such periods is implied. To test this hypothesis directly, we placed A. sagrei eggs in saltwater for 3 or 6 h with unimmersed eggs serving as the control. Hatching success and incubation time did not differ among the three treatments. These findings help explain the persistence of anole populations on small islands vulnerable to hurricanes.     

Systems analysis of primary Sjögren's syndrome pathogenesis in salivary glands identifies shared pathways in human and a mouse model

Bone tissue has an exceptional quality to regenerate to native tissue in response to injury. However, the fracture repair process requires mechanical stability or a viable biological microenvironment or both to ensure successful healing to native tissue. An improved understanding of the molecular and cellular events that occur during bone repair and remodeling has led to the development of biologic agents that can augment the biological microenvironment and enhance bone repair. Orthobiologics, including stem cells, osteoinductive growth factors, osteoconductive matrices, and anabolic agents, are available clinically for accelerating fracture repair and treatment of compromised bone repair situations like delayed unions and nonunions. Preclinical and clinical studies using biologic agents like recombinant bone morphogenetic proteins have demonstrated an efficacy similar or better than that of autologous bone graft in acute fracture healing. A lack of standardized outcome measures for comparison of biologic agents in clinical fracture repair trials, frequent off-label use, and a limited understanding of the biological activity of these agents at the bone repair site have limited their efficacy in clinical applications.     

How is extinction risk related to population-size variability over time? A family of models for species with repeated extinction and immigration

It is well known that for an isolated population, the probability of extinction is positively related to population size variation: more variation is associated with more extinction. What, then, is the relation of extinction to population size variation for a population embedded in a metapopulation and subjected to repeated extinction and recolonization? In this case, the extinction risk can be measured by the extinction rate, the frequency at which local extinction occurs. Using several population dynamics models with immigration, we find, in general, a negative correlation between extinction and variation. More precisely, with increasing length of the time series, an initially negative regression coefficient first becomes more negative, then becomes less negative, and eventually attains positive values before decreasing again to 0. This pattern holds under substantial variation in values of parameters representing species and environmental properties. It is also rather robust to census interval length and the fraction of missed individuals but fails to hold for high thresholds (population size values below which extinction is deemed to occur) when quasi extinction rather than true extinction is represented. The few departures from the initial negative correlation correspond to populations at risk: low growth rate or frequent catastrophes.     

Marine subsidies change short‐term foraging activity and habitat utilization of terrestrial lizards

Resource pulses are brief periods of unusually high resource abundance. While population and community responses to resource pulses have been relatively well studied, how individual consumers respond to resource pulses has received less attention. Local consumers are often the first to respond to a resource pulse, and the form and timing of individual responses may influence how the effects of the pulse are transmitted throughout the community. Previous studies in Bahamian food webs have shown that detritivores associated with pulses of seaweed wrack provide an alternative prey source for lizards. When seaweed is abundant, lizards (Anolis sagrei) shift to consuming more marine‐derived prey and increase in density, which has important consequences for other components of the food web. We hypothesized that the diet shift requires individuals to alter their habitat use and foraging activity and that such responses may happen very rapidly. In this study, we used recorded video observations to investigate the immediate responses of lizards to an experimental seaweed pulse. We added seaweed to five treatment plots for comparison with five control plots. Immediately after seaweed addition, lizards decreased average perch height and increased movement rate, but these effects persisted for only 2 days. To explore the short‐term nature of the response, we used our field data to parametrize heuristic Markov chain models of perch height as a function of foraging state. These models suggest a “Synchronized‐satiation Hypothesis,” whereby lizards respond synchronously and feed quickly to satiation in the presence of a subsidy (causing an initial decrease in average perch height) and then return to the relative safety of higher perches. We suggest that the immediate responses of individual consumers to resource pulse events can provide insight into the mechanisms by which these consumers ultimately influence community‐level processes.     

Targeting the cell cycle in breast cancer: towards the next phase

Deregulation of the cell cycle is a hallmark of cancer that enables limitless cell division. To support this malignant phenotype, cells acquire molecular alterations that abrogate or bypass control mechanisms in signaling pathways and cellular checkpoints that normally function to prevent genomic instability and uncontrolled cell proliferation. Consequently, therapeutic targeting of the cell cycle has long been viewed as a promising anti-cancer strategy. Until recently, attempts to target the cell cycle for cancer therapy using selective inhibitors have proven unsuccessful due to intolerable toxicities and a lack of target specificity. However, improvements in our understanding of malignant cell-specific vulnerabilities has revealed a therapeutic window for preferential targeting of the cell cycle in cancer cells, and has led to the development of agents now in the clinic. In this review, we discuss the latest generation of cell cycle targeting anti-cancer agents for breast cancer, including approved CDK4/6 inhibitors, and investigational TTK and PLK4 inhibitors that are currently in clinical trials. In recognition of the emerging population of ER+ breast cancers with acquired resistance to CDK4/6 inhibitors we suggest new therapeutic avenues to treat these patients. We also offer our perspective on the direction of future research to address the problem of drug resistance, and discuss the mechanistic insights required for the successful implementation of these strategies.