共查询到20条相似文献,搜索用时 15 毫秒
1.
L. P. Tatarinov 《Paleontological Journal》2011,45(1):1-4
In many animal groups, rudimentary organs of adult organisms appear at early stages of egg cleavage, when there is no trace
of morphological differentiation. More than half a century ago, I. I. Schmalhausen developed a profound concept of integrity
of the organism in the course of development. He emphasized that mutual adaptation of organs is based on correlations, involving
the so-called nonhereditary modifications, which are transformed into hereditary traits by means of natural selection. There
are many exceptions to the biogenetic law, as it was understood by de Beer. In particular, embryo of the pouched tree frog
Gastrotheca shows a retarded development and is spread over the yolk surface. As a result, it becomes similar somewhat to embryos of
amniotes. After the metamorphosis, Xenopus returns to ammonotelism. The integrity of ontogeny at the molecular level has much in common with the neutrality theory. 相似文献
2.
3.
Turtles are among the most intriguing amniotes but their communication and signaling have rarely been studied. Traditionally, they have been seen as basically just silent armored ‘walking stones’ with complex physiology but no altruism, maternal care, or aesthetic perception. Recently, however, we have witnessed a radical change in the perception of turtle behavioral and cognitive skills. In our study, we start by reviewing some recent findings pertaining to various highly developed behavioral and cognitive patterns with special emphasis on turtles. Then we focus on freshwater turtles and use data about their sexual behavior and size sexual dimorphism (SSD) to test whether conspicuous coloration of the head is in these animals related to sexual processes. We found that absence of aggressive mating behavior is statistically associated with the presence of conspicuous coloration on turtles’ heads. It also seems that while species with female-biased SSD are characterised by conspicuously colored head ornaments, in species with male-biased SSD conspicuous coloration is absent. Unlike large females, males thus seem to be under pressure to develop conspicuous coloration and engage in non-aggressive behavior using signaling to succeed in courtship. And finally, we discuss possible roles of head color patterns in turtle communication during mating. 相似文献
4.
Sexual dimorphism in body size (sexual size dimorphism) is common in many species. The sources of selection that generate the independent evolution of adult male and female size have been investigated extensively by evolutionary biologists, but how and when females and males grow apart during ontogeny is poorly understood. Here we use the hawkmoth, Manduca sexta, to examine when sexual size dimorphism arises by measuring body mass every day during development. We further investigated whether environmental variables influence the ontogeny of sexual size dimorphism by raising moths on three different diet qualities (poor, medium and high). We found that size dimorphism arose during early larval development on the highest quality food treatment but it arose late in larval development when raised on the medium quality food. This female-biased dimorphism (females larger) increased substantially from the pupal-to-adult stage in both treatments, a pattern that appears to be common in Lepidopterans. Although dimorphism appeared in a few stages when individuals were raised on the poorest quality diet, it did not persist such that male and female adults were the same size. This demonstrates that the environmental conditions that insects are raised in can affect the growth trajectories of males and females differently and thus when dimorphism arises or disappears during development. We conclude that the development of sexual size dimorphism in M. sexta occurs during larval development and continues to accumulate during the pupal/adult stages, and that environmental variables such as diet quality can influence patterns of dimorphism in adults. 相似文献
5.
Nicola Saino Maria Romano Diego Rubolini Celine Teplitsky Roberto Ambrosini Manuela Caprioli Luca Canova Kazumasa Wakamatsu 《PloS one》2013,8(2)
Melanin is the main pigment in animal coloration and considerable variation in the concentrations of the two melanin forms (pheo- and eumlanin) in pigmented tissues exists among populations and individuals. Melanin-based coloration is receiving increasing attention particularly in socio-sexual communication contexts because the melanocortin system has been hypothesized to provide a mechanistic basis for covariation between coloration and fitness traits. However, with few notable exceptions, little detailed information is available on inter-individual and inter-population variation in melanin pigmentation and on its environmental, genetic and ontogenetic components. Here, we investigate melanin-based coloration in an Italian population of a passerine bird, the barn swallow (Hirundo rustica rustica), its sex- and age-related variation, and heritability. The concentrations of eu- and pheomelanin in the throat (brown) and belly (white-to-brownish) feathers differed between sexes but not according to age. The relative concentration of either melanin (Pheo:Eu) differed between sexes in throat but not in belly feathers, and the concentrations in males compared to females were larger in belly than in throat feathers. There were weak correlations between the concentrations of melanins within as well as among plumage regions. Coloration of belly feathers was predicted by the concentration of both melanins whereas coloration of throat feathers was only predicted by pheomelanin in females. In addition, Pheo:Eu predicted coloration of throat feathers in females and that of belly feathers in males. Finally, we found high heritability of color of throat feathers. Melanization was found to differ from that recorded in Hirundo rustica rustica from Scotland or from H. r. erythrogaster from North America. Hence, present results show that pigmentation strategies vary in a complex manner according to sex and plumage region, and also among geographical populations, potentially reflecting adaptation to different natural and sexual selection regimes, and that some coloration components seem to be highly heritable. 相似文献
6.
Colombo G Orrù A Lai P Cabras C Maccioni P Rubio M Gessa GL Carai MA 《Molecular neurobiology》2007,36(1):102-112
Several lines of preclinical evidence indicate the ability of the prototypic cannabinoid CB1 receptor antagonist, rimonabant, to suppress various alcohol-related behaviors, including alcohol drinking and seeking behavior
and alcohol self-administration in rats and mice. Together, these data—synthetically reviewed in the present paper—suggest
(a) the involvement of the cannabinoid CB1 receptor in the neural substrate controlling alcohol intake, alcohol reinforcement, and the motivational properties of alcohol
and (b) that rimonabant may constitute a new and potentially effective medication for the treatment of alcohol dependence. 相似文献
7.
M Johnsson I Gustafson CJ Rubin AS Sahlqvist KB Jonsson S Kerje O Ekwall O Kämpe L Andersson P Jensen D Wright 《PLoS genetics》2012,8(8):e1002914
Domestication is one of the strongest forms of short-term, directional selection. Although selection is typically only exerted on one or a few target traits, domestication can lead to numerous changes in many seemingly unrelated phenotypes. It is unknown whether such correlated responses are due to pleiotropy or linkage between separate genetic architectures. Using three separate intercrosses between wild and domestic chickens, a locus affecting comb mass (a sexual ornament in the chicken) and several fitness traits (primarily medullary bone allocation and fecundity) was identified. This locus contains two tightly-linked genes, BMP2 and HAO1, which together produce the range of pleiotropic effects seen. This study demonstrates the importance of pleiotropy (or extremely close linkage) in domestication. The nature of this pleiotropy also provides insights into how this sexual ornament could be maintained in wild populations. 相似文献
8.
Rune Knudsen Per-Arne Amundsen Anders Klemetsen 《Environmental Biology of Fishes》2002,64(1-3):257-265
A long-term field study of a perturbed host–helminth system provides indirect evidence that a long-lived swimbladder nematode, Cystidicola farionis, induces mortality of Arctic charr, Salvelinus alpinus. The prevalence and abundance of this parasite has changed little over the period from 1987 to 1999. The cumulative numbers of L3-stage larvae steadily increased with increasing host age, indicating a continuous exposure to infection throughout the life of the target fish host. Indirect methods, which used data pooled over years and long-term cohort analyses, indicate that parasite-induced host mortality (PIHM) occurs in hosts older than 10 years. Furthermore, using a short-term cohort method adjusted for worm recruitment, we found indications of PIHM occurrence even in younger age groups. These patterns do not seem to be caused by high parasite mortality rates since dead worms are rarely observed inside the swimbladder. Age-related changes in infection rates or in resistance to infection seem to play only a minor role as there were only slight changes in the preference of charr for feeding on amphipods (which are intermediate hosts) and in the acquisition rate of L3 larvae in older hosts. Mortality of the most heavily infected hosts is the most probable explanation for the observed patterns. 相似文献
9.
Kaye Goddard &Alicia Mathis 《Ethology : formerly Zeitschrift fur Tierpsychologie》2000,106(7):631-643
Male longear sunfish, Lepomis megalotis , have longer opercular flaps than females, and females are known to prefer males with longer flaps, suggesting that these exaggerated structures serve as sexual ornaments. We tested the hypothesis that opercular flap length is associated with body condition and is therefore potentially an honest indicator of male quality. Opercular flaps grew significantly faster than pelvic fin spines, a non-sexually selected trait, regardless of diet treatment, suggesting an advantage to having fast-growing opercular flaps. Growth indices (opercular flap growth divided by pelvic fin spine growth) of males fed a larger ration were greater than those of males fed a smaller ration, although the difference was marginally non-significant. We also tested for an effect of opercular flap length on resource holding power by manipulating flap length on pairs of males matched for body length. In an experiment where opercular flaps were clipped to different lengths, only longer original (unmanipulated) flap length was associated with a significantly greater frequency of dominance. In a corollary experiment where opercular flaps were artificially lengthened, the abnormally long-flapped males were dominant significantly more often than the 'normal' males given transparent extensions. These results indicate that the opercular flap length of male longear sunfish may serve as an honest indicator of male quality and may be used to assess the resource holding power of rival males. 相似文献
10.
11.
《Ethology and sociobiology》1995,16(5):355-383
Across two studies, 716 and 308 undergraduate students from the United States and mainland China, respectively, were administered a series of measures on jealousy, emotional responses to partner infidelity, family background, and personality. Across both studies for the U.S. and Chinese samples, a higher proportion of males than females reported more distress to a partner's imagined sexual infidelity than to emotional infidelity, whereas a higher proportion of females than males reported more distress to a partner's emotional infidelity than to sexual infidelity, consistent with theoretical expectations and previous empirical research. However, a much higher proportion of U.S. males and females reported more distress to sexual infidelity than their same-sex Chinese peers, suggesting that the tendency toward sexual jealousy might be facultatively influenced by sexual permissiveness in the general culture. The overall pattern of results is considered in terms of individual and contextual differences in the expression of jealousy, as well as in terms of the emotional and behavioral responses associated with jealousy reactions. 相似文献
12.
Genital coevolution between the sexes is expected to be common because of the direct interaction between male and female genitalia during copulation. Here we review the diverse mechanisms of genital coevolution that include natural selection, female mate choice, male–male competition, and how their interactions generate sexual conflict that can lead to sexually antagonistic coevolution. Natural selection on genital morphology will result in size coevolution to allow for copulation to be mechanically possible, even as other features of genitalia may reflect the action of other mechanisms of selection. Genital coevolution is explicitly predicted by at least three mechanisms of genital evolution: lock and key to prevent hybridization, female choice, and sexual conflict. Although some good examples exist in support of each of these mechanisms, more data on quantitative female genital variation and studies of functional morphology during copulation are needed to understand more general patterns. A combination of different approaches is required to continue to advance our understanding of genital coevolution. Knowledge of the ecology and behavior of the studied species combined with functional morphology, quantitative morphological tools, experimental manipulation, and experimental evolution have been provided in the best-studied species, all of which are invertebrates. Therefore, attention to vertebrates in any of these areas is badly needed.Of all the evolutionary interactions between the sexes, the mechanical interaction of genitalia during copulation in species with internal fertilization is perhaps the most direct. For this reason alone, coevolution between genital morphologies of males and females is expected. Morphological and genetic components of male and female genitalia have been shown to covary in many taxa (Sota and Kubota 1998; Ilango and Lane 2000; Arnqvist and Rowe 2002; Brennan et al. 2007; Rönn et al. 2007; Kuntner et al. 2009; Tatarnic and Cassis 2010; Cayetano et al. 2011; Evans et al. 2011, 2013; Simmons and García-González 2011; Yassin and Orgogozo 2013; and see examples in Taxa Male structures Female structures Evidence Likely mechanism References Mollusks Land snails (Xerocrassa) Spermatophore-producing organs Spermatophore-receiving organs Comparative among species SAC or female choice Sauder and Hausdorf 2009 Satsuma Penis length Vagina length Character displacement Lock and key Kameda et al. 2009 Arthropods Arachnids (Nephilid spiders) Multiple Multiple Comparative among species SAC Kuntner et al. 2009 Pholcidae spiders Cheliceral apophysis Epigynal pockets Comparative (no phylogenetic analysis) Female choice Huber 1999 Harvestmen (Opiliones) Hardened penes and loss of nuptial gifts Sclerotized pregenital barriers Comparative among species SAC Burns et al. 2013 Millipedes Parafontaria tonominea Gonopod size Genital segment size Comparative in species complex Mechanical incompatibility resulting from Intersexual selection Sota and Tanabe 2010 Antichiropus variabilis Gonopod shape and size Accesory lobe of the vulva and distal projection Functional copulatory morphology Lock and key Wojcieszek and Simmons 2012 Crustacean Fiddler crabs, Uca Gonopode Vulva, vagina, and spermatheca Two-species comparison, shape correspondence Natural selection against fluid loss, lock and key, and sexual selection Lautenschlager et al. 2010 Hexapodes Odonates Clasping appendages Abdominal shape and sensory hairs Functional morphology, comparative among species Lock and key via female sensory system Robertson and Paterson 1982; McPeek et al. 2009 Insects Coleoptera: seed beetles Spiny aedagus Thickened walls of copulatory duct Comparative among species SAC Rönn et al. 2007 Callosobruchus: Callosobruchus maculatus Damage inflicted Susceptibility to damage Full sib/half sib mating experiments SAC Gay et al. 2011 Reduced spines No correlated response Experimental evolution SAC Cayetano et al. 2011 Carabid beetles (Ohomopterus) Apophysis of the endophallus Vaginal appendix (pocket attached to the vaginal apophysis) Cross-species matings Lock and key Sota and Kubota 1998; Sasabi et al. 2010 Dung beetle: Onthophagus taurus Shape of the parameres in the aedagus Size and location of genital pits Experimental evolution Female choice Simmons and García-González 2011 Diptera: Drosophila santomea and D. yakuba Sclerotized spikes on the aedagus Cavities with sclerotized platelets Cross-species matings SAC Kamimura 2012 Drosophila melanogaster species complex Epandrial posterior lobes
Oviscapt pouches Comparative among species SAC or female choice Yassin and Orgogozo 2013 Phallic spikes Oviscapt furrows Cercal teeth, phallic hook, and spines Uterine, vulval, and vaginal shields D. mauritiana and D. sechelia Posterior lobe of the genital arch Wounding of the female abdomen Mating with introgressed lines SAC Masly and Kamimura 2014 Stalk-eyed flies (Diopsidae) Genital process Common spermathecal duct Comparative among species and morphological Female choice Kotrba et al. 2014 Tse-tse flies: Glossina pallidipes Cercal teeth Female-sensing structures Experimental copulatory function Female choice Briceño and Eberhard 2009a,b Phelebotomine: sand flies Aedagal filaments, aedagal sheaths Spermathecal ducts length, base of the duct Comparative among species None specified Ilango and Lane 2000 Heteroptera: Bed bugs (Cimiciidae) Piercing genitalia Spermalege (thickened exosqueleton) Comparative among species SAC Carayon 1966; Morrow and Arnqvist 2003 Plant bugs (Coridromius) Changes in male genital shape External female paragenitalia Comparative among species SAC Tatarnic and Cassis 2010 Waterstriders (Gerris sp.) Grasping appendages Antigrasping appendages Comparative among species SAC Arnqvist and Rowe 2002 Gerris incognitus Grasping appendages Antigrasping appendages Comparative among populations SAC Perry and Rowe 2012 Bee assassins (Apiomerus) Aedagus Bursa copulatrix Comparative among species None Forero et al. 2013 Cave insects (Psocodea), Neotrogla Male genital chamber Penis-like gynosome Comparative among species Female competition (role reversal), coevolution SAC Yoshizawa et al. 2014 Butterflies (Heliconiinae) Thickness of spermatophore wall Signa: Sclerotized structure to break spermatophores Comparative among species SAC Sánchez and Cordero 2014 Fish Basking shark: Cetorhinus maximus Clasper claw Thick vaginal pads Morphological observation None Matthews 1950 Gambusia Gonopodial tips Genital papillae within openings Comparative among species Strong character displacement Langerhans 2011 Poecilia reticulata Gonopodium tip shape Female gonopore shape Comparative among populations SAC Evans et al. 2011 Reptiles Anoles Hemipene shape Vagina shape Shape correspondence, two species Sexual selection Köhler et al. 2012 Several species Hemipene shape Vagina shape Shape correspondence Lock and key, female choice, and SAC Pope 1941; Böhme and Ziegler 2009; King et al. 2009 Asiatic pit vipers Spininess in hemipenes Thickness of vagina wall Two-species comparison None Pope 1941 Garter snake: Thamnophis sirtalis Basal hempene spine Vaginal muscular control Experimental manipulation SAC Friesen et al. 2014 Birds Waterfowl Penis length Vaginal elaboration Comparative among species SAC Brennan et al. 2007 Tinamous Penis length/presence Vaginal elaboration Comparative among species Female choice/natural selection PLR Brennan, K Zyscowski, and RO Prum, unpubl. Mammals Marsupials Bifid penis Two lateral vaginae Shape correspondence None Renfree 1987 Equidna Bifid penis with four rosettes Single vagina splits into two uteri Shape correspondence None Augee et al. 2006; Johnston et al. 2007 Insectivores: Short-tailed shrew: Blarina brevicauda S-shaped curve of the erect penis Coincident curve in the vagina Shape correspondence None Bedford et al. 2004 Common tenrec: Tenrec caudatus Filiform penis (up to 70% of the male’s body length) Internal circular folds in the vagina Length correspondence None Bedford et al. 2004 Rodents: Cape dune mole: Bathyergus suillus Penis and baculum length Vaginal length Allometric relationships within species None Kinahan et al. 2007 Australian hopping mice (Notomys) Spiny penis Derived distal region in the vagina Morphological observation and two-species comparison Copulatory lock Breed et al. 2013 Pig: Sus domesticus Filiform penis end Cervical ridges Artificial insemination Female choice Bonet et al. 2013 Primates: Macaca arctoides Long and filamentous glans Vestibular colliculus (fleshy fold) that partially obstructs the entrance to the vagina Shape correspondence and comparison with close relatives None Fooden 1967