scholarly journals Vitrification of manually stage-selected embryos of Drosophila have significantly higher survival and emergence – Consequences for insect germplasm storage

Cryobiology ◽  
2022 ◽  
Author(s):  
Korie M. DeBardlabon ◽  
Arun Rajamohan ◽  
Joseph P. Rinehart
Keyword(s):  
2019 ◽  
Author(s):  
Robert L. Jarret ◽  
◽  
Noelle L. Anglin ◽  
David Ellis ◽  
Arthur Villordon ◽  
...  

The sweetpotato (Ipomoea batatas (L.) Lam.) is the sixth most important food crop on a global scale. While China accounts for about 80% of global production, Nigeria, Uganda, Indonesia and Tanzania are also large producers of sweetpotato. The chapter examines the origin and dispersal of sweetpotato, including archaeological data for the early distribution of the crop, before moving on to considering its general botany. The chapter considers in vitro germplasm storage in sweetpotato genebanks, as well as issues of quality control. The chapter looks at the importance of managing sweetpotato crop wild relatives (CWR) and examines plant quarantine and phytosanitary issues and the status of genebanks under international treaties. The chapter considers a number of specific issues associated with sweetpotato germplasm. Finally, the chapter looks at the application of next-generation sequencing to sweetpotato and its CWR, before looking ahead to future trends in this area.


1970 ◽  
Vol 7 ◽  
pp. 1-6
Author(s):  
Steve Adkins ◽  
Sarah Ashmore ◽  
Philip Cameron ◽  
Jason Halford ◽  
Leon Beyleveld

The ‘Queensland Seeds for Life Project (Q-SFL)’ is collaboration between the Millennium Seed Bank Project (MSBP) of the Royal Botanic Gardens, Kew, United Kingdom and several Australian Institutes, including The University of Queensland. The purpose of the SFL program is to improve the conservation and restoration of plant biodiversity in Queensland. This will be achieved by the collection and long-term storage of seed (as well as DNA) from priority species and by the use of these species in scientific research and utilization programs. In the first phase, seed of c. 1,000 species of Queensland native plants have been collected with c. 750 new to the MSBP. Germination tests have been completed for more than c. 600 collections, improving the knowledge base for these species and raising the opportunity for sustainable utilization in our collaborations with the Australian Mining, Floriculture and Native Fruits Industries. Detailed experiments have resolved germination issues (e.g. seed dormancy) for 200 species within families and genera that have been notoriously difficult to germinate, providing better understanding and management of threatened species. Work has been undertaken on the conservation of recalcitrant species with storage and regeneration protocols being developed for a number of previously unstudied species. Under the Q-SFL project six PhD studies have been completed on topics such as native grass utilization, soil seed banks, seed dormancy, seed longevity, utilization of native fruits and long term germplasm storage using cryopreservation. Our plan for the future builds on improving the cooperative nature of our partnership so that our state team can work in a complementary fashion with those from other states and overseas to obtain effective outcomes.DOI: 10.3126/botor.v7i0.4367 Botanica Orientalis – Journal of Plant Science (2010) 7: 1–6


HortScience ◽  
1996 ◽  
Vol 31 (3) ◽  
pp. 447-448 ◽  
Author(s):  
Erik J. Sacks ◽  
Dina A. St. Clair

The influence of cryogenic pollen storage on fruit set and seed production in tomato (Lycopersicon esculentum Mill.) was investigated. Flowers pollinated with pollen samples stored for 5 weeks at –80C, with or without 20 h precooling at 4C, had similar fruit set and number of viable seed per fruit as those pollinated with fresh pollen. Pollen samples, which were repeatedly cooled (–80C) and warmed (to 22 to 24C) for up to six cycles, continuously maintained the same viability as the fresh pollen. When cryogenically stored pollen of L. esculentum 2-837, LA359, LA3198, and LA3199 were used to pollinate LA359, the number of viable seed formed per fruit differed significantly. Results of this study suggest that pollen cryopreservation can be used successfully for tomato breeding and germplasm storage.


1994 ◽  
pp. 195-230 ◽  
Author(s):  
K. K. Kartha ◽  
F. Engelmann
Keyword(s):  

2019 ◽  
Vol 101 (3) ◽  
pp. 514-525 ◽  
Author(s):  
Pierre Comizzoli ◽  
William V Holt

Abstract Because of higher extinction rates due to human and natural factors, more basic and applied research in reproductive biology is required to preserve wild species and design proper strategies leading to sustainable populations. The objective of the review is to highlight recent, inspiring breakthroughs in wildlife reproduction science that will set directions for future research and lead to more successes in conservation biology. Despite new tools and approaches allowing a better and faster understanding of key mechanisms, we still know little about reproduction in endangered species. Recently, the most striking advances have been obtained in nonmammalian species (fish, birds, amphibians, or corals) with the development of alternative solutions to preserve fertility or new information about parental nutritional influence on embryo development. A novel way has also been explored to consider the impact of environmental changes on reproduction—the allostatic load—in a vast array of species (from primates to fish). On the horizon, genomic tools are expected to considerably change the way we study wildlife reproduction and develop a concept of “precision conservation breeding.” When basic studies in organismal physiology are conducted in parallel, new approaches using stem cells to create artificial gametes and gonads, innovations in germplasm storage, and more research on reproductive microbiomes will help to make a difference. Lastly, multiple challenges (for instance, poor integration of new tools in conservation programs, limited access to study animals, or few publication options) will have to be addressed if we want reproductive biology to positively impact conservation of biodiversity.


CORD ◽  
2014 ◽  
Vol 30 (2) ◽  
pp. 12
Author(s):  
H D D Bandupriya

Coconut is both socially and economically important crop in tropical and subtropical countries, thus the conservation of existing diversity of its germplasm is vital to maintain biodiversity, sustain crop production and utilisation of germplasm for crop improvement strategies. The recalcitrant storage behavior and large size of the coconut seed make it impossible to use as a germplasm storage material. Cryopreservation is an ideal means of long-term storage of germplasm which offers long-term storage capability with minimal storage space and maintenance requirements. The coconut embryo has been now adapted by various researchers for the purpose of germplasm exchange and it is now being routinely applied in germplasm collection and exchange activities with sufficient germination rates. The aim of the present study was to determine the effect of different coconut embryo transport/ storage methods [as solid endosperm plugs under cold temperature, embryos cultured in Solidified Agar Medium (SAM) or KCl solution under room temperature] on cryopreservation of plumules using encapsulation/dehydration method. The results revealed that plumules excised from embryos transported/ stored in SAM and pretreated with 1.0M sucrose could be cryopreserved with 71.8% survival and 56% recovery rates. The survival and recovery could be further increased up to 77.5% and 65% respectively by supplementation of 1.0M sucrose with 20 µM ABA.


2018 ◽  
Vol 19 (3) ◽  
pp. 724-729
Author(s):  
DINI HERVANI ◽  
DARDA EFENDI ◽  
M. RAHMAD SUHARTANTO ◽  
BAMBANG S. PURWOKO

Hervani D, Efendi D, Suhartanto MR, Purwoko BS. 2018. The preservation of somatic embryos of papaya derived from papaya lateral shoots after being stored in cryopreservation to maintain plant genetic information in the future. Biodiversitas 19: 724729. Germplasm storage of papaya is very important because this plant easily adapts to genetic changes due to environmental conditions and open system pollination, so it is necessary to retain the current genetics resources in order to conserve the genetic information. The storage of the vegetative part of the plant with cryopreservation is expected to retain the plant's genetic information in the future. Cryopreservation is the method for germplasm storage using liquid nitrogen at temperature of -196oC This experiment aimed to obtain the growth ability of papaya lateral shoots to produce somatic embryos after being stored by cryopreservation. The experiment was designed in factorial by Completely Randomized Design with two factors.The first factor was the immersion time duration in PVS2 as cryoprotectant solution with 5 treatments of immersion duration of 0, 10, 20, 30, and 40 minutes. Second factor was culture medium for cultivated the lateral shoot which was added with plant growth regulators such as BA (benzyl adenine) and NAA (naphthalene acetic acid) at levels of 0, 1, 2, 3, and 4 mg l-1, respectively. The results showed that the immersion of lateral shoot in cryoprotectants for 10 and 20 minutes gave the better plantlet survival rate after discharge from liquid nitrogen, while the treatment of culture media had not been significant difference.


2016 ◽  
Vol 64 (3) ◽  
pp. 260 ◽  
Author(s):  
B. Funnekotter ◽  
A. Sortey ◽  
E. Bunn ◽  
S. R. Turner ◽  
R. L. Mancera

Lomandra sonderi (F.Muell.) Ewart (Asparagaceae) is endemic to the south-west Western Australian jarrah (Eucalyptus marginata Donn ex Sm.) forest region, and is a difficult to propagate species important to post-mining restoration. Micropropagation is the only way to currently produce plants of this species for restoration. This study describes investigations into optimising cryopreservation for efficient long-term germplasm storage. In order to investigate the effect of preconditioning on post-cryogenic survival of shoot tips, in vitro grown plants were exposed to a range of light-, temperature- and osmotic-induced preconditioning treatments under culture room conditions for 3 weeks. Room temperature (24°C) preconditioning resulted in the greatest post-cryogenic survival, followed by low light (17 µmol m–2 s–1) preconditioning. Alternating temperature (25/5°C), high temperature (35°C), high sucrose (180 mM) and high light (93 µmol m–2 s–1) preconditioning treatments all led to significantly and progressively lower post-cryogenic shoot tip survival than room temperature preconditioning. Antioxidant activity of superoxide dismutase in preconditioned shoot tips showed a positive correlation to post-cryogenic survival overall, whereas the activities of glutathione reductase, glutathione peroxidase and catalase showed little correlation. Analysis throughout the cryopreservation protocol showed that the activity of glutathione reductase decreased significantly after cryopreservation, whilst the activity of glutathione peroxidase and catalase did not change.


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