Search results for "PARITY"
showing 10 items of 513 documents
The space-time relationship of taxonomic diversity and morphological disparity in the Middle Jurassic ammonite radiation.
2007
14 pages; International audience; The Middle Jurassic ammonite radiation (from the late Aalenian to the end of the mid-Bathonian) is traced using combined analyses of morphological disparity and taxonomic diversity. The global signals of disparity and diversity are compared. These signals are then broken down by paleogeographical provinces to detect any heterogeneity in the radiation. An examination of the global signals reveals three biodiversity crises (discordances between signals) where morphological disparity grows while taxonomic diversity declines. The subdivision of the signals indicates the radiation was heterogeneous between provinces: the global signal is an aggregate of signals …
Categorical versus geometric morphometric approaches to characterizing the evolution of morphological disparity in Osteostraci (Vertebrata, stem Gnat…
2020
Morphological variation (disparity) tends to be evaluated through two non-mutually exclusive approaches: (i) quantitatively, through geometric morphometrics, and (ii) in terms of discrete, ‘cladistic’, or categorical characters. Uncertainty over the comparability of these approaches diminishes the potential to obtain nomothetic insights into the evolution of morphological disparity, and the few benchmarking studies conducted so far show contrasting results. Here, we apply both approaches to characterising morphology in the stem-gnathostome vertebrate clade Osteostraci, in order to assess congruence between these alternative methods as well as to explore the evolutionary patterns of the grou…
Assessing metabolic constraints on the maximum body size of actinopterygians: locomotion energetics of Leedsichthys problematicus (Actinopterygii, Pa…
2018
Maximum sizes attained by living actinopterygians are much smaller than those reached by chondrichthyans. Several factors, including the high metabolic requirements of bony fishes, have been proposed as possible body‐size constraints but no empirical approaches exist. Remarkably, fossil evidence has rarely been considered despite some extinct actinopterygians reaching sizes comparable to those of the largest living sharks. Here, we have assessed the locomotion energetics of Leedsichthys problematicus, an extinct gigantic suspension‐feeder and the largest actinopterygian ever known, shedding light on the metabolic limits of body size in actinopterygians and the possible underlying factors th…
Oogenesis and reproductive investment of Atlantic herring are functions of not only present but long-ago environmental influences as well
2017
Following general life history theory, immediate reproductive investment (egg mass × fecundity/body mass) in oviparous teleosts is a consequence of both present and past environmental influences. This clarification questions the frequent use of season-independent (general) fecundity formulas in marine fish recruitment studies based on body metrics only. Here we test the underlying assumption of no lag effect on gametogenesis in the planktivorous, determinate-fecundity Atlantic herring (Clupea harengus) displaying large plasticity in egg mass and fecundity, examining Norwegian summer–autumn spawning herring (NASH), North Sea autumn-spawning herring (NSAH), and Norwegian spring-spawning herri…
Specimens at the Center: An Informatics Workflow and Toolkit for Specimen-level analysis of Public DNA database data
2016
Pham, Kasey K. [et al.]
Throwing down a genomic gauntlet on fisheries-induced evolution
2021
Beginning with studies on crypsis and camouflage, the hypothesis that predators can generate evolutionary change in their prey has a long and rich history (1). Few predators, however, rival humans in their potential to generate selection responses and concomitant phenotypic change on contemporary timescales. In the 1930s, J. B. S. Haldane (2) mused that fishing would be an ideal candidate for such “observable evolution” within a human lifetime, proceeding “with extreme and abnormal speed.” However, it was not until the late 1970s that research on fisheries-induced evolution (FIE) gained a substantive scientific foothold, beginning with thought-provoking work on Canadian whitefish ( Coregonu…
Thermal variability during ectotherm egg incubation: A synthesis and framework.
2020
Natural populations of ectothermic oviparous vertebrates typically experience thermal variability in their incubation environment. Yet an overwhelming number of laboratory studies incubate animals under constant thermal conditions that cannot capture natural thermal variability. Here, we systematically searched for studies that incubated eggs of ectothermic vertebrates, including both fishes and herpetofauna, under thermally variable regimes. We ultimately developed a compendium of 66 studies that used thermally variable conditions for egg incubation. In this review, we qualitatively discuss key findings from literature in the compendium, including the phenotypic effects resulting from diff…
Maternal effects on offspring Igs and egg size in relation to natural and experimentally improved food supply
2008
1. Maternal effects have been suggested to function as a mechanism for transgenerational plasticity, in which the environment experienced by the mother is translated into the phenotype of the offspring. In birds and other oviparous vertebrates where early development is within the egg, mothers may be able to improve the viability prospects of their offspring at hatching by priming eggs with immunological and nutritional components. 2. We studied how resource availability affects maternal investment in offspring by feeding Ural owl (Strix uralensis, Pall.) females prior to egg-laying in 3 years of dramatically different natural food conditions. 3. Supplementary feeding prior to laying increa…
Evolutionary population dynamics
2005
The interface between the evolution of life history traits and population dynamics in temporally and spatially variable environments is the topic of this chapter. Thus, the frame for the life history processes is set by spatial and temporal fluctuations in population density. Here, we will focus primarily on modes of reproduction and we are especially interested in whether alternative reproductive strategies can co-exist in a population. We show that spatially structured populations may allow co-existence of various life history strategies that do not easily co-exist in a nonstructured environment. Also, intrinsic and external temporal fluctuations in the environment tend to enhance polymor…
Length of activity season drives geographic variation in body size of a widely distributed lizard
2013
Understanding the factors that drive geographic variation in life history is an important challenge in evolutionary ecology. Here, we analyze what predicts geographic variation in life-history traits of the common lizard, Zootoca vivipara, which has the globally largest distribution range of all terrestrial reptile species. Variation in body size was predicted by differences in the length of activity season, while we found no effects of environmental temperature per se. Females experiencing relatively short activity season mature at a larger size and remain larger on average than females in populations with relatively long activity seasons. Interpopulation variation in fecundity was largely…