Showing posts with label Temperature. Show all posts
Showing posts with label Temperature. Show all posts

Breaking Barriers: How Seed Coat Removal Boosts Terminalia superba Germination | InformativeBD

The effect of seed coat removal on seed germination of Terminalia superba Engl. & Diels

Joseph M Asomaning, from the institute of Ghana. Padmore B Ansah, from the institute of Ghana and Naomi A Fosu, from the institute of Ghana. wrote a Research article about, Breaking Barriers: How Seed Coat Removal Boosts Terminalia superba Germination. Entitled, The effect of seed coat removal on seed germination of Terminalia superba Engl. & Diels. This research paper published by the Journalof Biodiversity and Environmental Sciences | JBES. an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

The influence of four constant temperatures: 20°C, 25°C, 30°C, 35°C and three germination media: 1% water agar, heat sterilized river sand and seed testing paper (STP) on the germination of decoated seeds of Terminalia superba Engl. & Diels. were investigated. The germination media were placed in 90 mm diameter plastic Petri dishes with seventy five decoated seeds in 3 replicates of 25 seeds. The statistical design used in the investigation was a completely randomized design in a 3 x 4 factorial (germination media × incubation temperatures). Decoated seeds of T. superba germinated at all the four temperatures investigated. The optimum temperatures were determined as 25°C, 30°C and 35°C. All the three media can be considered ideal for the reason that these temperatures interacted with the germination media to record germination percentages ranging from 73 to 89% in the study. Mean germination time (MGT) was significantly (p < 0.001) shorter when agar was used as germination media compared to when germination was carried out on STP and soil. The shapes of germination curves describing the cumulative germination of decoated seeds of T. superba at all temperatures and on all the germination media investigated are S-shaped.

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Introduction

Seed germination is controlled by several environmental factors, such as seed moisture content, temperature, and light. Seed condition also affects germination; for example, the seed coat may be water impermeable, or the mature seed may contain an underdeveloped embryo that only grows to full size after imbibition (Geneve, 2003). The seed coat represents a first line of defense against adverse external factors (helps protect the embryo from mechanical injury and from drying out) and also acts as channel for transmitting environmental cues to the interior of the seed (Radchuk and Borisjuk, 2014). Integrity of seed coat surface is extremely important for seed quality and fitness during seed storage or germination, and diverse technologies are available for preserving and enhancing of seed surface (Black and Halmer, 2006; Brooker et al., 2007).

That notwithstanding, an impermeable seed or fruit coat may impose physical dormancy which must be broken before water and air can reach the embryo and initiate germination (Baskin and Baskin, 2014). Most species have a seed coat which is impervious to water. This causes seed dormancy so that germination may extend over months or years. Example are the acacias and hence for their efficient germination at the nursery, it is necessary to apply some form of presowing treatment to ensure not only a high final germination percentage but rapid and uniform germination (Doran et al., 1983). The seeds of Prunus yedoensis also have slow and poor germination when intact. Decoating their seeds shortens the mean germination time (MGT) and improves seed germination percentage significantly. (Hyun Kim, 2019). Decoated seeds of Syzygium cumini germinated faster than coated seeds under nursery conditions, with high significant germination percentages, dry matter production rates and vigor indices (Sivasubramaniam and Selvarani, 2012).

Saeed and Thanos (2006) found seed coat to be inhibitory to the germination of Pinus gerardiana as removal of seed coat promoted both rate and final germination. Chika et al., 2020 reported that decoating seeds of Mansonia altissima improved their germination and resulted in the highest germination percentage. Bedada et al. (2018) also reported that de-coating improved germination and early nursery performance of Olea europaea.

Terminalia superba is one of the most heavily exploited African timber species, and locally, supplies have dwindled, with reports of declining populations in Côte d’Ivoire, Ghana, Nigeria, Cameroon and Congo (FAO,1984; N’Sosso, 1990). In Ghana, T. superba was one of the priority species earmarked for planting during the National Forest Plantation Development Programme launched in the year 2002. It is also on the list of priority species being planted under the on-going Ghana Forest Investment Programme. These developments have resulted in the need for sufficient quantities of good quality seeds to meet planting targets.

Cobbinah et al. (2001) and NTSC (2008) have reported days to first germination as 16 and 23 days respectively for seeds of T. superba sown intact. Unlike T. ivorensis, no serious dormancy problem has been reported about T. superba. However, pretreatment methods such as nicking or soaking in water have been recommended for faster and even germination (TTSA, 2010).

This study investigated the response of decoated seeds (seed with testa or seed coat removed) of T. superba to different temperatures and various germination media.

Reference

Asomaning JM, Sacande M, Olympio NS. 2011. Germination responses of Terminalia superba Engl. and Diels Seeds on the 2-Way Grant’s Thermogradient Plate. Research Journal of Seed Science 4(1), 28-39.

Asomaning JM. 2009. Seed desiccation tolerance and germination of seven important forest tree species in Ghana. PhD thesis. Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana. 1-187.

Association of Official Seed Analysts (AOSA). 1992. Rules for Testing Seeds. Journal of Seed Technology 6, 1-125.

Bahuguna VK, Rawat MMS, Joshi SR, Maithani GP. 1987. Studies on the viability, germination and longevity of Terminalia myriocarpa seed. Journal of Tropical Forestry 3(4), 318-323.

Baskin CC, Baskin JM. 2014. Seeds: In Ecology, Biogeography, and Evolution of Dormancy and Germination (second ed.), Academic Press, San Diego.

Bedada AB, Amsalu T, Ayele B. 2018. Effect of different seed treatments, provenance and size on germination and early establishment of Olea europaea. African Journal of Agricultural Research 13(40), 2163-2172.

Black MH, Halmer P. 2006. The Encyclopedia of Seeds: Science, Technology and Uses. Wallingford: CABI

Brooker NL, Lagalle CD, Zlatani A, Javni I, Petrovic Z. 2007. Soypolyol formulations as novel seed treatments for the management of soil-borne diseases of soybean. Communication. Agric. Appl. Biol. Sci 72, 35-43.

Chika PJ, Sakpere AM, Akinropo MS. 2020. Effect of pretreatments on germination of seeds of the timber plant, Terminalia ivorensis and Mansonia altissima (A. Chev.). Notulae Scientia Biologicae 12(2), 334-340

Cobbinah JR, Siaw DEKA, Gyimah A. 2001. Guide to tree planting in Ghana. Forestry Research Institute of Ghana 1-33.

Daws ML, Gaméné SC, Sacandé M, Pritchard HW, Groot PCG, Hoekstra F. 2004. Desiccation and storage of Lannea microcarpa seeds from Burkina Faso, pp 32-39. In:. Sacande M, Joker D. Dulloo ME, Thomsen K (eds). Comparative Storage Biology of Tropical Tree Seeds. IPGRI, Rome, 363 pp.

Doran JC, Turnbull JW, Boland DJ, Gunn BV. 1983. Handbook on seeds of dry-zone acacias: A guide for collecting, extracting, cleaning, and storing the seed and for treatment to promote germination of dry-zone acacias. Division of Forest Research, CSIRO, Canberra, AUSTRALIA.

Ellis RH, Roberts EH. 1981. The quantification of aging and survival in orthodox seeds. Seed Science and Technology 9, 373-409.

Food and Agriculture Organization (FAO). 1984. Report of the Fifth Session of FAO Panel of Experts on Forest Gene Resources. FAO, Rome.

Geneve RL. 2003. Impact of temperature on seed dormancy,” Hort Science 38(3), 336–341.

HyunKim D. 2019. Practical methods for rapid seed germination from seed coat- imposed dormancy of Prunus yedoensis. Scientia Horticulturae 243(3), 451-456.

International Seed Testing Association (ISTA). 1999. International rules for seed testing. ISTA, Zurich, Switzerland 1-133.

Masetto TE, Faria JM, Fraiz ACR. 2014. Re-induction of desiccation tolerance after germination of Cedrela fissilis Vell. Seeds. Annals of the Brazilian Academy of Sciences 86(3), 1273-1285

N’Sosso D. 1990. Le statut de conservation des bois tropicaux commercialisables. Rapport National Du Congo. ITTO Pre-Project

NTSC. 2008. Tree Seed Catalogue. The National Tree Seed Centre, Uganda 1-51.

Palazzo AJ, Brar GS. 1997. The effect of temperature on germination of eleven Festuca cultivars. Special Report 97-19. US Army Corps of Engineers. CRREL Technical Publications.

Radchuk V, Borisjuk L. 2014. Physical, metabolic and developmental functions of the seed coat. Frontiers in plant science 5, p.510.

Saeed M, Thanos CA. 2006. The effect of seed coat removal on seed germination of Pinus gerardiana Wallich ex D. Don. Chilgoza pine. Journal of Applied & Emerging Sciences 1(3), 174-177.

Shafii B, Price WJ. 2001. Estimation of cardinal temperatures in germination data analysis. Journal of Agricultural Biological and Environmental Statistics 6, 356-366

Silveira FAO, Fernandes GW. 2006. Effect of light, temperature and scarification on the germination of Mimosa foliolasa (Leguminasae) seeds. Seed Science and Technology 34, 585-592.

Sivasubramaniam K, Selvarani K. 2012. Viability and vigour of jamun (Syzygium cumini) seeds. Brazilian Journal of Botany 35(4), 397-400.

Tanzanian Tree Seed Agency (TTSA). 2010. Seed Catalogue. Tanzania Tree Seed Agency. 1-26.

Article sourceThe effect of seed coat removal on seed germination of Terminalia superba Engl. & Diels  

Growth Dynamics of Achatina fulica in a Controlled Breeding Environment | InformativeBD

Influence of temperature on survival, yolk utilization, growth, and morphometric anomaly rates in post-embryonic Clarias jaensis under controlled conditions

Boddis Zebaze Tsiguia,  Guegang Tekou, Fon Dorothy Engwali,  Mmira A Akohogni, Alexia Kévine Noubissi Chiassa,  Algrient Nana Towa, and Claudine Tekounegning Tiogué, from the institute of Cameroon. wrote a Research Article about, Growth Dynamics of Achatina fulica in a Controlled Breeding Environment . Entitled, Influence of temperature on survival, yolk utilization, growth, and morphometric anomaly rates in post-embryonic Clarias jaensis under controlled conditions. This research paper published by the International Journal of Agronomy and Agricultural Research (IJAAR). an open access scholarly research journal on Agronomy. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract  

Captive breeding of Clarias jaensis remains limited due to a lack of knowledge regarding optimal temperature conditions to ensure larval survival and early development. This study evaluated the impact of different temperatures on survival, yolk absorption, linear growth, and the rate of morphometric anomalies in post-embryos. A total of 580 newly hatched post-embryos were evenly distributed in 10 trays, placed in pairs in five polyester tanks. Each tank was subjected to one of the five experimental temperatures: 22°C, 25°C, 27°C, 29°C, and 31°C. Survival and anomaly rates were analyzed using the Kaplan-Meier test, while the evolution of yolk sac volume and larval length was studied using a one-factor ANOVA. The results show that the best survival rates were obtained at 25°C (96.5 ± 3.5%), 27°C (91.5 ± 6.4%), and 22°C (90 ± 2.8%). No survival was observed at 29°C and 31°C after three and two days post-hatching, respectively. Yolk absorption was significantly faster at 27°C (98.92 ± 0.58%), while differences in linear growth were not significant between 22°C, 25°C, and 27°C. The most frequent morphometric anomalies included pericardial edema, yolk edema, and skeletal deformities, with a lower malformation rate at 25°C (4.5%) compared to 22°C and 27°C. Based on these results, it is recommended to stabilize the breeding temperature at 25°C to maximize survival, and at 27°C to promote rapid growth and yolk absorption.

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Introduction

Clarias jaensis, an African catfish prized for its hardiness, rapid growth, and nutritional and cultural value, shows great potential for aquaculture (Angoni et al., 2016; Zango et al., 2016; Tiogue et al., 2020). However, despite this potential, mastering its rearing in controlled environments remains a major challenge, forcing fish farmers to rely on fry sourced from the wild (Pouomogne, 2008; Kenfack et al., 2019). This practice, in addition to limiting aquaculture production, places significant pressure on natural stocks, which are already weakened by overfishing and climate change. The provision of sufficient fry to meet the growing demand of fish farmers, therefore, depends on mastering the complete life cycle of C. jaensis, particularly its larval development in controlled conditions. Temperature is a key environmental factor in the early development of fish, significantly influencing their survival, growth, and morphogenesis (Cahu et al., 2003; Fontaine and Le Bail, 2004; Gatesoupe et al., 1999). The embryonic and larval stages, which are particularly vulnerable to environmental fluctuations, are especially sensitive to thermal variations. Understanding the influence of temperature on larval development is essential for optimizing farming practices and ensuring successful production in captivity. Previous studies on other Clariidae species, such as C. gariepinus (Legendre and Teugels, 1991; Chebel et al., 2005) and Heterobranchus bidorsalis (Olaniyi and Omitogun, 2013, 2014), have highlighted the significant impact of temperature on larval survival, growth, and development. However, the specific thermal tolerance of C. jaensis remains largely unknown. This study aims to fill this gap by rigorously evaluating the influence of temperature on the survival, yolk absorption, growth, and occurrence of morphometric anomalies in C. jaensis postembryos. By exposing the larvae to different temperatures in a controlled environment, we aim to identify the optimal thermal range that promotes their development and to understand the underlying mechanisms of the observed effects. The results of this research will have a dual impact. On one hand, they will provide basic information for improving the farming practices of C. jaensis in captivity, allowing for the adaptation of incubation and larval rearing conditions to maximize survival, growth, and fry quality. On the other hand, they will contribute to a better understanding of the biology of this species and its sensitivity to temperature variations, which is essential for the sustainable management of its natural populations in the face of climate change challenges.

Reference

Adewolu MA, Akintola SL, Akinwunmi OO. 2009. Growth performance and survival of hybrid African catfish larvae (Clarias gariepinus x Heterobranchus bidorsalis) fed on different diets. The Zoologist 7(1), 45–51.

Adewolu MA, Ogunsanmi AO, Yunusa A. 2008. Studies on growth performance and feed utilization of two Clariid catfish (Clarias gariepinus and Heterobranchus bidorsalis) fingerlings fed different dietary protein levels. Journal of Fisheries and Aquatic Science 3(1), 18–24.

Angoni DE, Eyango MT, Ambela D, Tchoumboué J. 2016. Effet de la densité de mise en charge sur les performances de croissance du poisson chat africain Clarias jaensis Boulanger, 1909 (Pisces: Clariidae) en étang. Innovative Space of Scientific Research Journals 16(130-03), 1–14.

Bagarinao T. 1986. Yolk resorption, onset of feeding and survival potential of larvae of three tropical marine fish species reared in the hatchery. Marine Biology 91, 449.

Bordin ER, Yamamoto FY, Mannes Y, Munhoz RC, Muelbert JRE, Freitas AM, Cestari MM, Ramsdorf WA. 2022. Sublethal effects of the herbicides atrazine and glyphosate at environmentally relevant concentrations on South American catfish (Rhamdia quelen) embryos. Environmental Toxicology and Pharmacology 104, 104057.

Cahu C, Zambonino-Infante JL, Takeuchi T. 2003. Nutritional components affecting skeletal development in fish larvae. Aquaculture 227(1-4), 245–258.

Chebel K, Patricia BD, Amirkolaie AK. 2005. Effects of temperature on survival, growth performance and feed utilization of African catfish (Clarias gariepinus) larvae. Aquaculture Research 36(8), 741–748.

Fiogbé ED, Kestemont P, Micha JC. 2003. Absorption du vitellus chez Heterobranchus longifilis. Journal of Fish Biology 62(3), 123–134.

Fiogbé ED, Kpanou JV, Kouassi N. 2003. Effet de la température sur la croissance larvaire de Heterobranchus longifilis (Valenciennes, 1840). Bulletin de la Recherche Agronomique du Bénin 39, 1–9.

Fontaine P, Le Bail P-Y. 2004. Domestication et croissance chez les poissons. INRA Productions Animales 17(3), 217–225.

Gatesoupe FJ. 1999. Ontogenèse, développement et physiologie chez les larves de poissons. Academia.edu.

Haylor GS, Mollah MFA. 1995. Controlled hatchery production of African catfish, Clarias gariepinus: The influence of temperature on early development. Aquatic Living Resources 8(4), 431–438.

Hecht T, Appelbaum S. 1988. Observations on the growth of juvenile African catfish, Clarias gariepinus (Burchell), in intensive culture. Aquaculture 74(3-4), 295–304.

Honji RM, Tolussi CE, Mello PH, Caneppele D, Moreira RG. 2012. Embryonic development and larval stages of Steindachneridion parahybae (Siluriformes: Pimelodidae) – implications for the conservation and rearing of this endangered Neotropical species. Neotropical Ichthyology 10(2), 313–327.

Hossain F, Islam SMM, Ashaf-Ud-Doulah M, Ali MS, Islam MS, Brown C, Shahjahan M. 2021. Influences of salinity on embryonic and larval development of striped catfish Pangasianodon hypophthalmus. Frontiers in Marine Science 8, 781951.

Jezierska B, Lugowska K, Witeska M, Sarnowski P. 2000. Malformations of newly hatched common carp larvae. Electron. J. Pol. Agric. Univ., Fisheries 3(2), 1–14.

Kamler E. 1992. Early life history of fish: An energetics approach. Springer Science & Business Media.

Kenfack Atangana J, Ducarme C, Micha JC. 2019. La pisciculture au Cameroun: bilan et perspectives. International Journal of Biological and Chemical Sciences 13(2), 1140.

Legendre M, Teugels GG. 1991. Développement et tolérance à la température des œufs de Heterobranchus longifilis et comparaison des développements larvaires de H. longifilis et de Clarias gariepinus (Teleostei, Clariidae). Aquatic Living Resources 4, 227–240.

Nguenga D, Breine JJ, Teugels GG, Ollevier F. 1996. Artificial propagation of the African catfish Heterobranchus longifilis (Siluroidei; Clariidae): Description of a simple technique to avoid sacrificing male broodfish for the obtention of milt. Aquaculture 143, 215–217.

Olaniyi WA, Omitogun OG. 2013. Stages in the early and larval development of the African catfish Clarias gariepinus (Teleostei, Clariidae). Zygote 21(3), 314–330.

Olaniyi WA, Omitogun OG. 2014. Embryonic and larval developmental stages of African giant catfish Heterobranchus bidorsalis (Geoffroy Saint Hilaire, 1809) (Teleostei, Clariidae). SpringerPlus 3, 677.

Pouomogne V. 2008. Capture-based aquaculture of Clarias catfish: case study of the Santchou fishers in western Cameroon. In A. Lovatelli and P.F. Holthus (eds). Capture-based aquaculture. Global overview. FAO Fisheries Technical Paper. No. 508. Rome, FAO. pp. 93–108.

Rahman MM, Habib MA, Hossain QZ, Siddiqui MN, Rahman MM, Ahsan MN. 2011. Embryonic development of Clarias batrachus under the influence of aeration and water flow. ECOPRINT 18, 25–31.

Shan X, Quan H, Dou S. 2008. Effects of delayed first feeding on growth and survival of rock bream Oplegnathus fasciatus larvae. Aquaculture 277, 14–23.

Tiogue CT, Nyadjeu P, Mouokeu SR, Tekou G, Tchoupou H. 2020. Evaluation of hybridization in two African catfishes (Siluriformes, Clariidae): Exotic (Clarias gariepinus Burchell, 1822) and native (Clarias jaensis Boulenger, 1909) species under controlled hatchery conditions in Cameroon. Advances in Agriculture 2020, Article ID 8985424, 11 pages.

Woynarovich E, Horváth L. 1980. The artificial propagation of warm-water finfishes: A manual for extension. FAO Fisheries Technical Paper No. 201. Rome: Food and Agriculture Organization of the United Nations.

Zango P, Tiogue CT, Nyadjeu P, Kenfack A, Tseuwo SGN, Kamanke SK, Kameni ABT, Tomedi ME, Tchoumboue J. 2023. Effect of the type of pituitary extracts and dose of synthetic hormones HCG and Ovaprim on some reproductive characteristics of the endogenous catfish of Cameroon Clarias jaensis (Boulanger, 1909) in a controlled environment. Asian Journal of Fisheries and Aquatic Research 25(5), 105–116.

Zango P, Tomedi Eyango MT, Efole TE, Tiogue CT, Nguenga D, Kamanke Kamanke SM, Mikolasek O, Tchoumboue J. 2016. Performances de reproduction du poisson chat endogène du Cameroun Clarias jaensis (Boulenger, 1909) en milieu contrôlé. International Journal of Biological and Chemical Sciences 10(2), 533–542.

SourceInfluence of temperature on survival, yolk utilization, growth, and morphometric anomalyrates in post-embryonic Clarias jaensis under controlled conditions