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1.
J Plant Res ; 137(5): 879-892, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39014142

ABSTRACT

Plant biomass allocation is mainly affected by the environment where each individual grows. In this sense, through the rapid global expansion of impermeable areas, urbanization has strong, albeit poorly understood, consequences on the biomass allocation of plants found in this environment. Nevertheless, the comprehension of biomass allocation processes in urban shrubs remains unclear, because most studies of urban ecology focus on tree species. This is an important gap of knowledge because a great part of urban vegetation is composed of shrubs and their association with trees have positive impacts in urban ecosystem services. In this study, we explored the ecological and potential selective pressure effects of an urbanization gradient on the biomass allocation patterns of aboveground organs of Turnera subulata, a widely distributed tropical shrub. We have demonstrated that, for certain reproductive organs, biomass allocation decreases in locations with higher urbanization. Unlike expected, the biomass of vegetative organs was not affected by urbanization, and we did not observe any effect of urbanization intensity on the variance in biomass allocation to vegetative and reproductive organs. We did not record urbanization-mediated trade-offs in biomass allocation for reproductive and vegetative organs. Instead, the biomass of these structures showed a positive relationship. Our data suggest that urbanization does not result in radical changes in biomass allocation of T. subulata, and neither in the variation of these traits. They indicate that the ability of T. subulata to thrive in urban environments may be associated with life history and morphological mechanisms. Our findings contribute to the understanding of shrub plant responses to urbanization and highlight urbanization as a potential factor in resource allocation differences for different structures and functions in plants living in these environments.


Subject(s)
Biomass , Turnera , Urbanization , Turnera/physiology , Turnera/growth & development , Tropical Climate , Ecosystem
2.
Ann Bot ; 131(5): 885-896, 2023 05 15.
Article in English | MEDLINE | ID: mdl-37004162

ABSTRACT

BACKGROUND AND AIMS: We examined the relationship between reproductive allocation and vegetative growth in three monoicous sexual systems of bryophytes. The sexual systems show a gradient of increasing distance between the sexes, from gonioautoicous to cladautoicous to rhizautoicous. Here, we investigated the following two hypotheses: (1) reproductive allocation differs between sexes and sexual systems, and male reproductive allocation increases with increasing distance between male and female gametangia; and (2) reproductive allocation is negatively related to vegetative growth. METHODS: We sampled the three sexual systems, represented by three moss species of the genus Fissidens in the Atlantic Forest of Southeastern Brazil. Ramets were washed in the laboratory; the reproductive structures were detached from the vegetative ramets and sorted regarding sex and individual, dried at 70 °C for 72 h, and weighed in an ultramicrobalance. We calculated the mean reproductive and vegetative mass and reproductive allocation and used generalized linear models to test our predictions. KEY RESULTS: Reproductive allocation differed between species and sexes. It was higher in the rhizautoicous than in the cladautoicous and gonioautoicous species. Mean reproductive allocation was greater in males than in females of the rhizautoicous species, greater in females than males of the cladautoicous species, and did not differ between the sexes in the gonioautoicous species. Estimates of reproductive and vegetative mass were positively related in females of the rhizautoicous species. Vegetative mass was not related to reproductive allocation in the gonioautoicous species, but negatively related to reproductive allocation in the male and female branchlets of the cladautoicous species and in the female ramets of the rhizautoicous species. CONCLUSIONS: The reproductive allocation patterns differ between the rhizautoicous species and the 'truly' monoicous species, with shorter intersexual distances, which implies that our hypotheses were supported only in part. We suggest that the hypotheses should be reformulated and tested further by comparing 'truly' monoicous species with dioicous species and by including other genera.


Subject(s)
Bryophyta , Bryopsida , Reproduction , Brazil , Forests
3.
Am J Bot ; 108(12): 2405-2415, 2021 12.
Article in English | MEDLINE | ID: mdl-34622937

ABSTRACT

PREMISE: Unlike most flowering plants, orchid flowers have under-developed ovules that complete development only after pollination. Classical studies reported variation in the stage in which ovule development is arrested, but the extent of this variation and its evolutionary and ecological significance are unclear. METHODS: Here, we used light microscopy to observe ovule development at anthesis for 39 species not previously studied and surveyed the literature gaining information on 94 orchid species. Tropical and temperate members of all five orchid subfamilies as well as species with contrasting pollination strategies (rewarding versus deceptive) and life forms (epiphytic versus terrestrial) were represented. We analyzed the data using statistical comparisons and a phylogenetic generalized least square (PGLS) analysis. RESULTS: Apostasioideae, the sister to the rest of the orchids, have mature ovules similar to other Asparagales, while under-differentiated ovules are present in the other subfamilies. Ovule developmental stages showed high variation even among closely related groups. Ovules were more developed in terrestrial than in epiphytic, in temperate than in tropical, and in rewarding than in deceptive pollination orchid species. This latter comparison was also significant in the PGLS analysis. CONCLUSIONS: These results suggest that ovule developmental stage in orchids can be shaped by ecological factors, such as seasonality and pollination strategy, and can be selected for optimizing female reproductive investment.


Subject(s)
Orchidaceae , Ovule , Flowers , Phylogeny , Pollination
4.
J Anim Ecol ; 85(4): 960-72, 2016 07.
Article in English | MEDLINE | ID: mdl-27119773

ABSTRACT

Explaining the remarkable variation in socially monogamous females' extrapair (EP) behaviour revealed by decades of molecular paternity testing remains an important challenge. One hypothesis proposes that restrictive environmental conditions (e.g. extreme weather, food scarcity) limit females' resources and increase EP behaviour costs, forcing females to reduce EP reproductive behaviours. For the first time, we tested this hypothesis by directly quantifying within-pair and EP behaviours rather than inferring behaviour from paternity. We evaluated whether warmer sea surface temperatures depress total pre-laying reproductive behaviours, and particularly EP behaviours, in socially paired female blue-footed boobies (Sula nebouxii). Warm waters in the Eastern Pacific are associated with El Niño Southern Oscillation and lead to decreased food availability and reproductive success in this and other marine predators. With warmer waters, females decreased their neighbourhood attendance, total copulation frequency and laying probability, suggesting that they contend with restricted resources by prioritizing self-maintenance and committing less to reproduction, sometimes abandoning the attempt altogether. Females were also less likely to participate in EP courtship and copulations, but when they did, rates of these behaviours were unaffected by water temperature. Females' neighbourhood attendance, total copulation frequency and EP courtship probability responded to temperature differences at the between-season scale, and neighbourhood attendance and EP copulation probability were affected by within-season fluctuations. Path analysis indicated that decreased EP participation was not attributable to reduced female time available for EP activities. Together, our results suggest that immediate time and energy constraints were not the main factors limiting females' infidelity. Our study shows that El Niño conditions depress female boobies' EP participation and total reproductive activity. In addition to increasing general self-maintenance and reproductive costs, warm waters may increase costs specific to EP behaviours including divorce, reduced male parental care, or pathogen exposure. Our results suggest that female boobies strategically refrained from EP behaviours to avoid these or other longer-term costs, rather than being compelled by immediate constraints. This study demonstrates that current environmental conditions affect females' mating decisions, contributing to variation in EP behaviours, even in a long-lived, iteroparous species that can buffer against temporary adversity.


Subject(s)
Birds/physiology , El Nino-Southern Oscillation , Reproduction/physiology , Sexual Behavior, Animal/physiology , Temperature , Animals , Female , Male , Pacific Ocean
5.
Rev. biol. trop ; Rev. biol. trop;63(4)Oct.-Dec. 2015.
Article in English | LILACS-Express | LILACS | ID: biblio-1507455

ABSTRACT

The trade-off seed size/number is a recognized phenomenon capable of shaping ecological processes of colonization and establishment of plant species. Studies that describe trade-offs size/number of seeds in supra-annual fruiting species are still rare. In this study, two predictions for trade-off size/number hypothesis were tested: (i) on a population scale, seeds produced during years of greater reproductive investment showed reduced size, and (ii) on individual scale there is an inverse relationship between size and number of seeds produced by individual plant. To test these predictions, 102 Copaifera langsdorffii adult plants were monitored monthly from January to September during four consecutive years (2008 to 2011) in order to study the reproductive investment of plants. C. langsdorffii plants exhibited reproductive activity only during years 2008 and 2011. The mean number of seeds per branch was 26.4 % greater in 2008 comparatively to 2011. It was also observed that seed size was greater in the year of 2008, when plants produced greater number of fruits. Thus, the data did not support the first prediction of seed size/number hypothesis. In both reproductive years, there was a negative relationship between seed size and number of seeds, supporting the second prediction of the seed size/number hypothesis. The interaction term with the reproductive year suggests that the trade-off size/number of seeds was indeed stronger in 2011, when the plants produced lower seed number. Finally, this study calls the attention to supra-annual fruiting pattern in C. langsdoffii, and suggests that the phenological patterns contribute to explain the wide variation in their seed size and geographical distribution.


El compromiso o balance adaptativo de las semillas en tamaño/ número (trade-off seed size/number) es un reconocido fenómeno capaz de dar forma a los procesos ecológicos de la colonización y el establecimiento de especies de plantas. Los estudios que describen el compromiso adaptativo de las semillas en tamaño/número en especies con fructificación supra-anual siguen siendo raros. En este estudio, se probaron dos hipótesis predictivas para compromiso adap-tativo de las semillas en tamaño/número: (i) una a escala poblacional, semillas producidas durante el año de mayor inversión reproductiva mostraran un tamaño reducido, y (ii) otra a escala individual que se dará una relación inversa entre el tamaño y número de semillas producidas por la planta individual. Para probar estas predicciones, 102 plantas adultas de Copaifera langsdorffii fueron monitoreadas mensualmente entre enero y septiembre, durante cuatro años consecutivos (2008-2011) con el fin de estudiar la inversión reproductiva de las plantas. Plantas langsdorffii C. exhibieron actividad reproductiva sólo durante el 2008 y 2011. El número promedio de semillas por rama fue 26.4 % mayor en 2008 en comparación con 2011. También se observó que el tamaño de la semilla fue mayor en 2008, cuando las plantas producen mayor número de frutos. Por lo tanto, los datos no apoyan la primera hipótesis de predicción de tamaño/número. En ambos años reproductivos, existía una relación negativa entre el tamaño de la semilla y el número de semillas, comprobando la segunda hipótesis de predicción del tamaño/número de semillas. El periodo de interacción con el año reproductivo sugiere que el compromiso adaptativo de las semillas en tamaño/número fue de hecho más fuerte en 2011, cuando las plantas produjeron baja cantidad de semillas. Por último, este estudio llama la atención por el patrón de fructificación supra-anual en C. langsdoffii, y sugiere que los patrones fenológicos contribuyen a explicar la amplia variación en el tamaño de la semilla y la distribución geográfica.

6.
Article in English | VETINDEX | ID: vti-440981

ABSTRACT

We present new data on litter size and date of birth (month) for 21 South American scorpions species. We provide data for one katoikogenic species, the liochelid Opisthacanthus cayaporum Vellard, 1932 (offspring = 3; birth month: Jan); and for several apoikogenic species, such as the bothriurids Bothriurus araguayae Vellard, 1934 (53; Sep), B. rochensis San Martín, 1965 (22-28; Jan, Aug); the buthids Ananteris balzanii Thorell, 1891 (10-34; Jan-Mar), Physoctonus debilis (Koch, 1840) (2; Sep), Rhopalurus amazonicus Lourenço, 1986 (19; Nov), R. lacrau Lourenço & Pinto-da-Rocha, 1997 (30; Dec), R. laticauda Thorell, 1876 (41; Nov), R. rochai Borelli, 1910 (11-47; Dec-Jan, Mar-Apr), Tityus bahiensis (Perty, 1833) (4-23; Oct-Mar), T. clathratus Koch, 1844 (8-18; Nov-Jan), T. costatus (Karsch, 1879) (21-25; Jan, Apr), T. kuryi Lourenço, 1997 (4-16; Mar), T. mattogrossensis Borelli, 1901(8-9; May), T. obscurus (Gervais, 1843) (16-31; Jan-Feb, May, Jul), T. serrulatus Lutz & Mello, 1922 (8-36; Dec, Feb-Apr), T. silvestris Pocock, 1897 (5-14; Dec-Jan, Apr), T. stigmurus (Thorell, 1876) (10-18; Nov, Jan, Mar), Tityus sp. 1 (T. clathratus group - 7-12; Feb-Apr), Tityus sp. 2 (T. bahiensis group - 2; Mar); and the chactid Brotheas sp. (8-21; Jan, Apr). We observed multiple broods: R. lacrau (offspring in the 2nd brood = 27), T. kuryi (6-16), T. obscurus (2-32), T. silvestris (8), T. stigmurus (4-9), T. bahiensis (offspring in the 2nd brood = 2-18; 3rd = 1), and T. costatus (2nd brood = 18; 3rd = 4). We found statistically significant positive correlation between female size and litter size for T. bahiensis and T. silvestris, and nonsignificant correlation for T. serrulatus.

7.
Article in English | VETINDEX | ID: vti-689989

ABSTRACT

We present new data on litter size and date of birth (month) for 21 South American scorpions species. We provide data for one katoikogenic species, the liochelid Opisthacanthus cayaporum Vellard, 1932 (offspring = 3; birth month: Jan); and for several apoikogenic species, such as the bothriurids Bothriurus araguayae Vellard, 1934 (53; Sep), B. rochensis San Martín, 1965 (22-28; Jan, Aug); the buthids Ananteris balzanii Thorell, 1891 (10-34; Jan-Mar), Physoctonus debilis (Koch, 1840) (2; Sep), Rhopalurus amazonicus Lourenço, 1986 (19; Nov), R. lacrau Lourenço & Pinto-da-Rocha, 1997 (30; Dec), R. laticauda Thorell, 1876 (41; Nov), R. rochai Borelli, 1910 (11-47; Dec-Jan, Mar-Apr), Tityus bahiensis (Perty, 1833) (4-23; Oct-Mar), T. clathratus Koch, 1844 (8-18; Nov-Jan), T. costatus (Karsch, 1879) (21-25; Jan, Apr), T. kuryi Lourenço, 1997 (4-16; Mar), T. mattogrossensis Borelli, 1901(8-9; May), T. obscurus (Gervais, 1843) (16-31; Jan-Feb, May, Jul), T. serrulatus Lutz & Mello, 1922 (8-36; Dec, Feb-Apr), T. silvestris Pocock, 1897 (5-14; Dec-Jan, Apr), T. stigmurus (Thorell, 1876) (10-18; Nov, Jan, Mar), Tityus sp. 1 (T. clathratus group - 7-12; Feb-Apr), Tityus sp. 2 (T. bahiensis group - 2; Mar); and the chactid Brotheas sp. (8-21; Jan, Apr). We observed multiple broods: R. lacrau (offspring in the 2nd brood = 27), T. kuryi (6-16), T. obscurus (2-32), T. silvestris (8), T. stigmurus (4-9), T. bahiensis (offspring in the 2nd brood = 2-18; 3rd = 1), and T. costatus (2nd brood = 18; 3rd = 4). We found statistically significant positive correlation between female size and litter size for T. bahiensis and T. silvestris, and nonsignificant correlation for T. serrulatus.

8.
Article in English | LILACS-Express | VETINDEX | ID: biblio-1503699

ABSTRACT

We present new data on litter size and date of birth (month) for 21 South American scorpions species. We provide data for one katoikogenic species, the liochelid Opisthacanthus cayaporum Vellard, 1932 (offspring = 3; birth month: Jan); and for several apoikogenic species, such as the bothriurids Bothriurus araguayae Vellard, 1934 (53; Sep), B. rochensis San Martín, 1965 (22-28; Jan, Aug); the buthids Ananteris balzanii Thorell, 1891 (10-34; Jan-Mar), Physoctonus debilis (Koch, 1840) (2; Sep), Rhopalurus amazonicus Lourenço, 1986 (19; Nov), R. lacrau Lourenço & Pinto-da-Rocha, 1997 (30; Dec), R. laticauda Thorell, 1876 (41; Nov), R. rochai Borelli, 1910 (11-47; Dec-Jan, Mar-Apr), Tityus bahiensis (Perty, 1833) (4-23; Oct-Mar), T. clathratus Koch, 1844 (8-18; Nov-Jan), T. costatus (Karsch, 1879) (21-25; Jan, Apr), T. kuryi Lourenço, 1997 (4-16; Mar), T. mattogrossensis Borelli, 1901(8-9; May), T. obscurus (Gervais, 1843) (16-31; Jan-Feb, May, Jul), T. serrulatus Lutz & Mello, 1922 (8-36; Dec, Feb-Apr), T. silvestris Pocock, 1897 (5-14; Dec-Jan, Apr), T. stigmurus (Thorell, 1876) (10-18; Nov, Jan, Mar), Tityus sp. 1 (T. clathratus group - 7-12; Feb-Apr), Tityus sp. 2 (T. bahiensis group - 2; Mar); and the chactid Brotheas sp. (8-21; Jan, Apr). We observed multiple broods: R. lacrau (offspring in the 2nd brood = 27), T. kuryi (6-16), T. obscurus (2-32), T. silvestris (8), T. stigmurus (4-9), T. bahiensis (offspring in the 2nd brood = 2-18; 3rd = 1), and T. costatus (2nd brood = 18; 3rd = 4). We found statistically significant positive correlation between female size and litter size for T. bahiensis and T. silvestris, and nonsignificant correlation for T. serrulatus.

9.
Article in English | LILACS-Express | VETINDEX | ID: biblio-1484059

ABSTRACT

Sexual and asexual reproduction and associated population dynamics were investigated in the colonial ascidian Didemnum rodriguesi Rocha & Monniot, 1993 (Didemnidae) in southern Brazil. Investment in sexual (production of new individuals) and asexual (colony growth) reproduction was compared between seasons. Permanently marked quadrats were repeatedly photographed to measure changes in colonies. Eggs and larvae were counted monthly in collected colonies. This species alternates seasonally between sexual (summer) and asexual (winter) reproduction. In summer, colonies were smaller, brooded eggs and larvae and recruitment rates were greater, while in winter, colony size was larger and eggs and larvae were absent. There is a relationship between fecundity and colony area. Fragmentation and fusion of colonies were similar in summer and winter, as well as mortality. In conclusion, D. rodriguesi has a lifecycle usual for high latitude ascidians with a limited time length for sexual reproduction and alternate investment in sexual and asexual reproduction along the year.


Reprodução sexuada e assexuada, mortalidade e a dinâmica de fusões e fissões de colônias de Didemnum rodriguesi Rocha & Monniot, 1993 foram investigados e comparados no sul do Brasil, no inverno e verão. Tais eventos foram analisados por fotografias de áreas permanentemente demarcadas e coletas mensais de colônias. Os resultados indicam que esta espécie alterna sazonalmente a reprodução sexuada (verão) e assexuada (inverno). Durante o verão as colônias são mais abundantes e menores, com ovos e larvas incubados e taxas de recrutamento maiores. No inverno há um menor número de colônias, porém de maior tamanho e inférteis. Existe uma relação entre fecundidade e tamanho da colônia. Não foram encontradas diferenças estatísticas no número de eventos de fragmentação e fusão entre o verão e inverno, bem como para mortalidade. Conclui-se que esta espécie tem um ciclo de vida típico de espécies de maiores latitudes, com tempo limitado para a reprodução sexuada e alternância no investimento entre reprodução sexuada e assexuada.

10.
Article in English | VETINDEX | ID: vti-437665

ABSTRACT

Sexual and asexual reproduction and associated population dynamics were investigated in the colonial ascidian Didemnum rodriguesi Rocha & Monniot, 1993 (Didemnidae) in southern Brazil. Investment in sexual (production of new individuals) and asexual (colony growth) reproduction was compared between seasons. Permanently marked quadrats were repeatedly photographed to measure changes in colonies. Eggs and larvae were counted monthly in collected colonies. This species alternates seasonally between sexual (summer) and asexual (winter) reproduction. In summer, colonies were smaller, brooded eggs and larvae and recruitment rates were greater, while in winter, colony size was larger and eggs and larvae were absent. There is a relationship between fecundity and colony area. Fragmentation and fusion of colonies were similar in summer and winter, as well as mortality. In conclusion, D. rodriguesi has a lifecycle usual for high latitude ascidians with a limited time length for sexual reproduction and alternate investment in sexual and asexual reproduction along the year.


Reprodução sexuada e assexuada, mortalidade e a dinâmica de fusões e fissões de colônias de Didemnum rodriguesi Rocha & Monniot, 1993 foram investigados e comparados no sul do Brasil, no inverno e verão. Tais eventos foram analisados por fotografias de áreas permanentemente demarcadas e coletas mensais de colônias. Os resultados indicam que esta espécie alterna sazonalmente a reprodução sexuada (verão) e assexuada (inverno). Durante o verão as colônias são mais abundantes e menores, com ovos e larvas incubados e taxas de recrutamento maiores. No inverno há um menor número de colônias, porém de maior tamanho e inférteis. Existe uma relação entre fecundidade e tamanho da colônia. Não foram encontradas diferenças estatísticas no número de eventos de fragmentação e fusão entre o verão e inverno, bem como para mortalidade. Conclui-se que esta espécie tem um ciclo de vida típico de espécies de maiores latitudes, com tempo limitado para a reprodução sexuada e alternância no investimento entre reprodução sexuada e assexuada.

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