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121 results for “reproductive seasonality”

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edi56/100

Individual plant growth and reproduction in the black sand extended growing season experiment for East Knoll, Audubon, Lefty, and Trough sites, 2018 - 2020.

As a result of climate change, the Rocky Mountain Front Range is experiencing warmer summers and earlier snowmelt. Due to the importance of snow for regulating soil temperature, growing season length, and available moisture in alpine ecosystems, even small shifts in the snow-free period could have large impacts. The focus of the Black Sand Extended Growing Season Length Experiment is to examine how terrain-related differences in climate exposure influence the way alpine habitats respond to climate change via earlier snowmelt. To simulate how climate exposure may affect plant communities, NWT LTER researchers established 5 experimental sites, each containing a pair 10 x 40m rectangular plots. These sites include north and south facing aspects, subalpine and alpine tundra meadows and a range of hydrological conditions (e.g. dry meadows, moist meadows, wet meadows). We accelerated snowmelt in one plot at each site by adding chemically inert black sand, while keeping the second plot as an unmanipulated control; black sand was added to control plots after snow had naturally melted. We used open top warming chambers (OTCs) to increase summer temperature in three subplots within each of the 10 x 40 m plots. This dataset includes measurements of growth and reproduction for Geum plants as well as counts of buds and flowers were counted and recorded for each tagged study plant, within all snow and warming treatments at all sites except Soddie.

openCC (other)May 2024View details →
zenodo44/100

Supplementary datasets for manuscript titled: Seasonal tissue-specific gene expression in wild crown-of-thorns starfish reveals reproductive and stress-related transcriptional systems

<p>Supplementary datasets for manuscript titled: Seasonal tissue-specific gene expression in wild crown-of-thorns starfish reveals reproductive and stress-related transcriptional systems</p>

opencc-by-4.0Mar 2024View details →
zenodo40/100

Рис. 7. Сезонная Δинамика соΔержимого цист H. glycines Fig. 7. Seasonal dynamics of H. glycines cysts content in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions

Рис. 7. Сезонная Δинамика соΔержимого цист H. glycines Fig. 7. Seasonal dynamics of H. glycines cysts content

opencc-by-4.0Feb 2021View details →
zenodo40/100

Рис. 8. Изменение жизнеспособности цист Heterodera glycines на протяжении сезона размножения Fig. 8. Changes in the viability of Heterodera glycines cysts during the breeding season in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions

Рис. 8. Изменение жизнеспособности цист Heterodera glycines на протяжении сезона размножения Fig. 8. Changes in the viability of Heterodera glycines cysts during the breeding season

opencc-by-4.0Feb 2021View details →
zenodo40/100

Рис. 4. Сезонная Δинамика размеров цист Heterodera glycines и чисΛа яиц в них. Размер цист в баΛΛах: 1 — меΛкие, 2 — среΔние, 3 — крупные Fig. 4. Seasonal dynamics of the size of Heterodera glycines cysts and the number of eggs in them. The size of cysts in classes: 1 — small, 2 — medium, 3 — large in Reproductive potential of Soybean Cyst Nematode Heterodera glycines - quarantine pest of soybean - in Primorsky Region conditions

Рис. 4. Сезонная Δинамика размеров цист Heterodera glycines и чисΛа яиц в них. Размер цист в баΛΛах: 1 — меΛкие, 2 — среΔние, 3 — крупные Fig. 4. Seasonal dynamics of the size of Heterodera glycines cysts and the number of eggs in them. The size of cysts in classes: 1 — small, 2 — medium, 3 — large

opencc-by-4.0Feb 2021View details →
dryad40/100

Quantifying direct and indirect effects of early-season herbivory on reproduction across four brassicaceous plant species

<div> <p>Insect herbivores can directly affect plant reproduction by feeding on reproductive tissues, or indirectly by feeding on vegetative tissues for which plants are unable to compensate. Additionally, early-arriving herbivores may have cascading effects on plant reproduction by altering the later-arriving community. However, the dynamic interplay between plant development and the assembly of herbivore communities remains underexplored. Hence, it is unclear whether non-outbreak levels of ambient herbivory early in the development of plants can impact plant fitness and to what extent these effects are mediated through changes in plant development and subsequent herbivory. By excluding the herbivore community in an exclosure experiment and by manipulating early-season herbivory in a common garden field experiment replicated across four Brassicaceae species and two years, we tested whether early-season herbivory by caterpillars (<em>Pieris rapae)</em> or aphids (<em>Myzus persicae</em>) affected development, reproduction, and the herbivore communities associated with individual plants. In addition, we tested a causal hypothesis to assess the relative importance and temporal interplay between variation in herbivore communities and variation in plant development in determining plant reproduction. Early-season herbivory affected plant reproduction in the exclosure experiment, with effects being highly dependent on the plant species, the herbivore species, and the year. However, we found no such effects in the field experiment. The exploratory path analysis indicated that variation in plant reproduction is best predicted by variation in plant development, explaining 80% of the total effect on seed production. This suggests that early-season herbivory had limited effects on later plant development, and plants were able to attenuate the impact of early-season herbivory. However, no clear compensatory mechanism could be identified. While early-season herbivory has the potential to affect plant reproduction through changes in plant development or the subsequent development of the associated community, these effects were small and varied across closely related species. This suggests that plant species may be exposed to different levels of natural selection by early-season herbivores through plant- or community-mediated effects on reproduction.</p> </div>

opencc-zeroApr 2024View details →
zenodo40/100

Fig. 3 in How does diet influence the reproductive seasonality of tropical freshwater fish? A case study of a characin in a tropical mountain river

Fig. 3. Non-Metric Multi-Dimensional Scaling Ordination (NMDS) of monthly variations of the diet with respect to sex. Stress = 0.10. Filled symbols are the dry months.

opencc-by-4.0Dec 2009View details →
zenodo40/100

Fig. 2 in How does diet influence the reproductive seasonality of tropical freshwater fish? A case study of a characin in a tropical mountain river

Fig. 2. Monthly variation of prey types-IRI values. Rainfall follows a bimodal seasonal pattern (shadow on background). The asterisks show the months in which reproduction occurs.

opencc-by-4.0Dec 2009View details →
zenodo40/100

Fig. 1 in How does diet influence the reproductive seasonality of tropical freshwater fish? A case study of a characin in a tropical mountain river

Fig. 1. Ontogenetic and intersexual variation in the diet of Creagrutus guanes. Size classes correspond to standard length ranges: 3 = 21-30 mm; 4 = 31-40 mm; 5 = 41-50 mm; 6 = 51-60 mm; 7 = 61-70mm; 8 = 71-80mm.

opencc-by-4.0Dec 2009View details →
zenodo40/100

Fig. 2 in Reproductive seasonality of Geophagus steindachneri Eigenmann & Hildebrand, 1922 (Perciformes: Cichlidae) in a tropical mountain river

Fig. 2. Monthly variation in adult females: (a) SL, standard length and WE, eviscerated weight, (b) liver and fat weight, and (c) ovary weight. Barplot behind the lines represents the rainfall pattern.

opencc-by-4.0Jun 2015View details →
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Fig. 5 in Reproductive seasonality of Geophagus steindachneri Eigenmann & Hildebrand, 1922 (Perciformes: Cichlidae) in a tropical mountain river

Fig. 5. Monthly variation in adult males: (a) SL, standard length and WE, eviscerated weight, (b) liver and fat weight, and (c) testis weight. Barplot behind the lines represents the rainfall pattern.

opencc-by-4.0Jun 2015View details →
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Fig. 3 in Reproductive seasonality of Geophagus steindachneri Eigenmann & Hildebrand, 1922 (Perciformes: Cichlidae) in a tropical mountain river

Fig. 3. Monthly variation in (a) the frequency of ovarian development stages and (b) the frequency of mouthbrooding females carrying embryos, larvae, or juveniles.

opencc-by-4.0Jun 2015View details →
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Fig. 1 in Reproductive seasonality of Geophagus steindachneri Eigenmann & Hildebrand, 1922 (Perciformes: Cichlidae) in a tropical mountain river

Fig. 1. Monthly variation of environmental variables: (a) rainfall pattern, (b) pH and temperature, and (c) conductivity and transparency.

opencc-by-4.0Jun 2015View details →
zenodo40/100

Fig. 4 in Reproductive seasonality of Geophagus steindachneri Eigenmann & Hildebrand, 1922 (Perciformes: Cichlidae) in a tropical mountain river

Fig. 4. Differences between females that were not performing parental care and mouth-brooding females: (a) stage of ovary maturity, with circle size indicating number of females in each condition; (b) liver and ovary weight.

opencc-by-4.0Jun 2015View details →
zenodo40/100

Figure 3 in Seasonal hormones, female reproductive tract changes, and some field observations on breeding activities of the small Indian mongoose (Herpestes javanicus) from its native range of Potohar Plateau, Pakistan

Figure 3. Light microscopic (hematoxylin and eosin stained) sections (40×) of the ovaries of female small Indian mongoose (Herpestes javanicus) from the Potohar Plateau, Pakistan: A) showing 3 Graafian follicles indicative of the state of preovulation during February 2013; B) events of early gestation period during March 2013, corpus luteum of moderate size and reddish yellow, antrum being a bit convoluted in structure rather than being complete; C) events of late gestation period during April 2013, whereby corpora lutea are seen as the most prominent structures; D) showing lactation phase of the species with no corpora lutea or ripe follicles during June 2013. (*P.F.: primary follicle; S.F.: secondary follicle; C.L.: corpus luteum; G.F.: Graafian follicle; Pr. F.: primordial follicle).

opencc-by-4.0Dec 2016View details →
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Figure 4. A in Seasonal hormones, female reproductive tract changes, and some field observations on breeding activities of the small Indian mongoose (Herpestes javanicus) from its native range of Potohar Plateau, Pakistan

Figure 4. A) Foot prints of small Indian mongoose established around its burrow, B) Especially designed mesh trap for live capturing of the species, C) Placental Scars, D) Developing embryos inside the uteri of female mongoose exposed after dissection, E) A vigilant mongoose, F) Small Indian mongoose and her pups caught in a live trap

opencc-by-4.0Dec 2016View details →
zenodo40/100

Figure 2 in Seasonal hormones, female reproductive tract changes, and some field observations on breeding activities of the small Indian mongoose (Herpestes javanicus) from its native range of Potohar Plateau, Pakistan

Figure 2. Levels (mIU/mL) of follicle stimulating hormone (FSH) and luteinizing hormone (LH) in plasma samples of small Indian mongoose females (Herpestes javanicus) trapped on the Potohar Plateau. LH levels show 2 peaks (1 in September 2012 and 1 in March 2013).

opencc-by-4.0Dec 2016View details →
zenodo40/100

Fig. 5 in Selection and use of calling site by Boana leptolineata and Phyllomedusa distincta during the reproductive season

Fig. 5. Selection of microhabitat demonstrated by the dispersion diagram of the Procrustes analysis (ss, sum of squares; t0, Correlation of Procrustes. For each capture event: circles represents the matrix with environmental variables from the occupied quadrants; arrows represents the matrix of available quadrants with the same variables; line between both represents the size of congruence between matrices).

opencc-by-4.0Jun 2021View details →
zenodo40/100

Fig. 4 in Selection and use of calling site by Boana leptolineata and Phyllomedusa distincta during the reproductive season

Fig. 4. Perch characteristics of Phyllomedusa distincta (B. Lutz, 1950) and Boana leptolineata (P. Braun &amp; C. Braun, 1977) in RPPN PrÓ-Mata, São Francisco de Paula, RS, Brazil. (points: average; bars: standard error).

opencc-by-4.0Jun 2021View details →
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Fig. 3 in Selection and use of calling site by Boana leptolineata and Phyllomedusa distincta during the reproductive season

Fig. 3. Microhabitat strata heterogeneity of Phyllomedusa distincta (B. Lutz, 1950) and Boana leptolineata (P. Braun &amp; C. Braun, 1977) in RPPN PróMata, São Francisco de Paula, RS, Brazil (Cv: stratum height coefficient of variation; points: average; bars: standard error).

opencc-by-4.0Jun 2021View details →

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allen-brain-atlas
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Last verified 2026-04-30Open record

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Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

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Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record