Indehiscent • Dry Fruits That Do Not Split at Maturity
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Advanced Encryption Standard Real-World Alternatives
Outline Multiple Encryption Birthday Attack Advanced Encryption Standard Real-World Alternatives CPSC 367: Cryptography and Security Michael Fischer Lecture 7 February 5, 2019 Thanks to Ewa Syta for the slides on AES CPSC 367, Lecture 7 1/58 Outline Multiple Encryption Birthday Attack Advanced Encryption Standard Real-World Alternatives Multiple Encryption Composition Group property Birthday Attack Advanced Encryption Standard AES Real-World Issues Alternative Private Key Block Ciphers CPSC 367, Lecture 7 2/58 Outline Multiple Encryption Birthday Attack Advanced Encryption Standard Real-World Alternatives Multiple Encryption CPSC 367, Lecture 7 3/58 Outline Multiple Encryption Birthday Attack Advanced Encryption Standard Real-World Alternatives Composition Composition of cryptosystems Encrypting a message multiple times with the same or different ciphers and keys seems to make the cipher stronger, but that's not always the case. The security of the composition can be difficult to analyze. For example, with the one-time pad, the encryption and decryption functions Ek and Dk are the same. The composition Ek ◦ Ek is the identity function! CPSC 367, Lecture 7 4/58 Outline Multiple Encryption Birthday Attack Advanced Encryption Standard Real-World Alternatives Composition Composition within practical cryptosystems Practical symmetric cryptosystems such as DES and AES are built as a composition of simpler systems. Each component offers little security by itself, but when composed, the layers obscure the message to the point that it is difficult for an adversary to recover. The trick is to find ciphers that successfully hide useful information from a would-be attacker when used in concert. CPSC 367, Lecture 7 5/58 Outline Multiple Encryption Birthday Attack Advanced Encryption Standard Real-World Alternatives Composition Double Encryption Double encryption is when a cryptosystem is composed with itself. -
Implementations of Block Cipher SEED on Smartphone Operating Systems
SECURWARE 2011 : The Fifth International Conference on Emerging Security Information, Systems and Technologies Implementations of Block Cipher SEED on Smartphone Operating Systems HwanJin Lee, DongHoon Shin, and Hyun-Chul Jung Security R&D Team Korea Internet & Security Agency (KISA) Seoul, Korea {lhj79, dhshin, hcjung}@kisa.or.kr Abstract—As more and more people are using smartphones limited power and offers inferior performance compared to a these days, a great deal of important information, such as PC. Therefore, it is difficult to use an open cryptographic personal information and the important documents of library such as OpenSSL, which is designed for the PC corporations among other things, are being saved on environment, in a smartphone. We need to study on the way smartphones. Unlike a PC, people can access another person’s for the effective use of SEED in smartphone. smartphone without great difficulty, and there is a high This paper presents the results of implementing the block possibility of losing one’s smartphone. If smartphone is lost cipher SEED to a smartphone. The results of a comparison without encryption, important information can be exploited. In with open cryptographic libraries (OpenSSL, BouncyCastle) addition, the open cryptographic library for PCs cannot be will also be presented. The SEED is a block cipher used due to the limited performance of the smartphone. This established as an international standard ISO/IEC and the paper introduces the optimization implementation technique for the smartphone OS and the results of using that technique. Korean standard. Section 2 introduces the SEED and open In addition, the results of a speed comparison with the open cryptographic libraries; Section 3 introduces smartphone cryptographic library will be presented. -
Samara Newsletter July & August 2020
SamaraThe International Newsletter of the Millennium Seed Bank Partnership Special issue featuring projects and research from The Global Tree Seed Bank Programme, funded by the Garfield Weston Foundation August/September 2020 Issue 35 ISSN 1475-8245 Juglans pyriformis in the State of Veracruz Conserving and investigating native tree seeds to support community-based reforestation initiatives in Mexico Veracruz Pronatura Photo: Mexico is the fourth richest country in the world in terms of plant Millennium Seed Bank. Seed research has species diversity, after Brazil, China, and Colombia with a flora of been carried out on 314 species to study ca. 23,000 vascular plants. Around half of the plant species are their tolerance to desiccation for seed endemic and nearly 3,500 are trees. banking and to determine germination requirements to inform propagation activities. One of the key project species ELENA CASTILLO-LORENZO (Latin America Projects Coordinator, RBG Kew), MICHAEL WAY is Cedrela odorata (Spanish cedar), whose (Conservation Partnership Coordinator (Americas, RBG Kew) & TIZIANA ULIAN (Senior Research conservation status is vulnerable (IUCN Leader – Diversity and Livelihoods, RBG Kew) 2020) due to exploitation for its highly Trees and forests provide multiple goods Iztacala of the Universidad Autónoma valued wood. C. odorata is also used for and benefits for humans, such as high- de México (Fes-I UNAM). The aim medicinal purposes by local communities quality wood, fruit, honey, and other of this project was to conserve tree in Mexico, with the leaves being prepared ecosystem services, including clean water, species through a collaborative research in herbal tea to treat toothache, earache, prevention of soil erosion and mitigation of programme focusing on endemic, and intestinal infections. -
Using Address Independent Seed Encryption and Bonsai Merkle Trees to Make Secure Processors OS- and Performance-Friendly ∗
Using Address Independent Seed Encryption and Bonsai Merkle Trees to Make Secure Processors OS- and Performance-Friendly ∗ Brian Rogers, Siddhartha Chhabra, Yan Solihin Milos Prvulovic Dept. of Electrical and Computer Engineering College of Computing North Carolina State University Georgia Institute of Technology {bmrogers, schhabr, solihin}@ncsu.edu [email protected] Abstract and feasible threat is physical or hardware attacks which involve placing a bus analyzer that snoops data communicated between the In today’s digital world, computer security issues have become processor chip and other chips [7, 8]. Although physical attacks increasingly important. In particular, researchers have proposed may be more difficult to perform than software-based attacks, they designs for secure processors which utilize hardware-based mem- are very powerful as they can bypass any software security protec- ory encryption and integrity verification to protect the privacy and tion employed in the system. The proliferation of mod-chips that integrity of computation even from sophisticated physical attacks. bypass Digital Rights Management protection in game systems has However, currently proposed schemes remain hampered by prob- demonstrated that given sufficient financial payoffs, physical attacks lems that make them impractical for use in today’s computer sys- are very realistic threats. tems: lack of virtual memory and Inter-Process Communication Recognizing these threats, computer architecture researchers support as well as excessive storage and performance overheads. have recently proposed various types of secure processor architec- In this paper, we propose 1) Address Independent Seed Encryption tures [4, 5, 13, 14, 16, 17, 18, 19, 20, 22, 23, 24, 25, 26]. Secure pro- (AISE), a counter-mode based memory encryption scheme using a cessors assume that off-chip communication is vulnerable to attack novel seed composition, and 2) Bonsai Merkle Trees (BMT), a novel and that the chip boundary provides a natural security boundary. -
Fruits: Kinds and Terms
FRUITS: KINDS AND TERMS THE IMPORTANT PART OF THE LIFE CYCLE OFTEN IGNORED Technically, fruits are the mature ovaries of plants that contain ripe seeds ready for dispersal • Of the many kinds of fruits, there are three basic categories: • Dehiscent fruits that split open to shed their seeds, • Indehiscent dry fruits that retain their seeds and are often dispersed as though they were the seed, and • Indehiscent fleshy fruits that turn color and entice animals to eat them, meanwhile allowing the undigested seeds to pass from the animal’s gut We’ll start with dehiscent fruits. The most basic kind, the follicle, contains a single chamber and opens by one lengthwise slit. The columbine seed pods, three per flower, are follicles A mature columbine follicle Milkweed seed pods are also large follicles. Here the follicle hasn’t yet opened. Here is the milkweed follicle opened The legume is a similar seed pod except it opens by two longitudinal slits, one on either side of the fruit. Here you see seeds displayed from a typical legume. Legumes are only found in the pea family Fabaceae. On this fairy duster legume, you can see the two borders that will later split open. Redbud legumes are colorful before they dry and open Lupine legumes twist as they open, projecting the seeds away from the parent The bur clover modifies its legumes by coiling them and providing them with hooked barbs, only opening later as they dry out. The rattlepods or astragaluses modify their legumes by inflating them for wind dispersal, later opening to shed their seeds. -
FIPS 140-2 Non-Proprietary Security Policy Oracle Linux 7 NSS
FIPS 140-2 Non-Proprietary Security Policy Oracle Linux 7 NSS Cryptographic Module FIPS 140-2 Level 1 Validation Software Version: R7-4.0.0 Date: January 22nd, 2020 Document Version 2.3 © Oracle Corporation This document may be reproduced whole and intact including the Copyright notice. Title: Oracle Linux 7 NSS Cryptographic Module Security Policy Date: January 22nd, 2020 Author: Oracle Security Evaluations – Global Product Security Contributing Authors: Oracle Linux Engineering Oracle Corporation World Headquarters 500 Oracle Parkway Redwood Shores, CA 94065 U.S.A. Worldwide Inquiries: Phone: +1.650.506.7000 Fax: +1.650.506.7200 oracle.com Copyright © 2020, Oracle and/or its affiliates. All rights reserved. This document is provided for information purposes only and the contents hereof are subject to change without notice. This document is not warranted to be error-free, nor subject to any other warranties or conditions, whether expressed orally or implied in law, including implied warranties and conditions of merchantability or fitness for a particular purpose. Oracle specifically disclaim any liability with respect to this document and no contractual obligations are formed either directly or indirectly by this document. This document may reproduced or distributed whole and intact including this copyright notice. Oracle and Java are registered trademarks of Oracle and/or its affiliates. Other names may be trademarks of their respective owners. Oracle Linux 7 NSS Cryptographic Module Security Policy i TABLE OF CONTENTS Section Title -
Morphological, Anatomical, and Taxonomic Studies in Anomochloa and Streptochaeta (Poaceae: Bambusoideae)
SMITHSONIAN CONTRIBUTIONS TO BOTANY NUMBER 68 Morphological, Anatomical, and Taxonomic Studies in Anomochloa and Streptochaeta (Poaceae: Bambusoideae) Emmet J. Judziewicz and Thomas R. Soderstrom SMITHSONIAN INSTITUTION PRESS Washington, D.C. 1989 ABSTRACT Judziewicz, Emmet J., and Thomas R. Soderstrom. Morphological, Anatomical, and Taxonomic Studies in Anomochloa and Streptochaeta (Poaceae: Bambusoideae). Smithsonian Contributions to Botany, number 68,52 pages, 24 figures, 1 table, 1989.-Although resembling the core group of the bambusoid grasses in many features of leaf anatomy, the Neotropical rainforest grass genera Anomochloa and Streptochaeta share characters that are unusual in the subfamily: lack of ligules, exceptionally long microhairs with an unusual morphology, a distinctive leaf blade midrib structure, and 5-nerved coleoptiles. Both genera also possess inflorescences that are difficult to interpret in conventional agrostological terms. Anomochloa is monotypic, and A. marantoidea, described in 1851 by Adolphe Brongniart from cultivated material of uncertain provenance, was rediscovered in 1976 in the wet forests of coastal Bahia, Brazil. The inflorescence terminates in a spikelet and bears along its rachis several scorpioid cyme-like partial inflorescences. Each axis of a partial inflorescence is subtended by a keeled bract and bears as its first appendages two tiny, unvascularized bracteoles attached at slightly different levels. The spikelets are composed of an axis that bears two bracts and terminates in a flower. The lower, chlorophyllous, deciduous spikelet bract is separated from the coriaceous, persistent, corniculate upper bract by a cylindrical, indurate internode. The flower consists of a low membrane surmounted by a dense ring of brown cilia (perigonate annulus) surrounding the andrecium of four stamens, and an ovary bearing a single hispid stigma. -
Plant Anatomy Lab 13 – Seeds and Fruits
Plant Anatomy Lab 13 – Seeds and Fruits In this (final) lab, you will be observing the structure of seeds of gymnosperms and angiosperms and the fruits of angiosperms. Much of the work will be done with a dissecting microscope, but a few prepared slides will also be used. A set of photocopied images from the plant anatomy atlas will be available as a handout. You can use the handout to help you identify the various structures we will be looking at in seeds and fruits. Also, a fruit key is available as a separate handout. Remember that we will be considering only a small fraction of the structural diversity present among seeds of gymnosperms and the seeds and fruits of angiosperms. Seeds Gymnosperms Obtain a prepared slide of an immature pine ovule and of a mature pine ovule. You will be able to tell them apart from the following observations. • Looking at the immature ovule, you will see a megagametophyte with one or more archegonia at the end near the micropyle. The egg inside may or may not have been fertilized. • Also find the nucellus and integument tissues. Next look at a slide of a mature ovule. Instead of the megagametophyte, you will find a developing embryo. As part of this embryo, find the • cotyledons, • the radicle (embryonic root), and the • shoot apical meristem. Depending on its age, you may also notice procambial strands running between the embryonic root and the shoot apex. Points to consider: We might say that gymnosperms and angiosperms have seeds but only angiosperms have fruits - Why is that? Why don’t we consider the seed cone of a pine tree a fruit? Angiosperms Dicot Obtain a bean pod. -
Mistaken Identity? Invasive Plants and Their Native Look-Alikes: an Identification Guide for the Mid-Atlantic
Mistaken Identity ? Invasive Plants and their Native Look-alikes an Identification Guide for the Mid-Atlantic Matthew Sarver Amanda Treher Lenny Wilson Robert Naczi Faith B. Kuehn www.nrcs.usda.gov http://dda.delaware.gov www.dsu.edu www.dehort.org www.delawareinvasives.net Published by: Delaware Department Agriculture • November 2008 In collaboration with: Claude E. Phillips Herbarium at Delaware State University • Delaware Center for Horticulture Funded by: U.S. Department of Agriculture Natural Resources Conservation Service Cover Photos: Front: Aralia elata leaf (Inset, l-r: Aralia elata habit; Aralia spinosa infloresence, Aralia elata stem) Back: Aralia spinosa habit TABLE OF CONTENTS About this Guide ............................1 Introduction What Exactly is an Invasive Plant? ..................................................................................................................2 What Impacts do Invasives Have? ..................................................................................................................2 The Mid-Atlantic Invasive Flora......................................................................................................................3 Identification of Invasives ..............................................................................................................................4 You Can Make a Difference..............................................................................................................................5 Plant Profiles Trees Norway Maple vs. Sugar -
Structure, Physical Characteristics, and Com- Position of the Pericarp and Integument of Johnson Grass Seed in Relation to Its Physiology 1
STRUCTURE, PHYSICAL CHARACTERISTICS, AND COM- POSITION OF THE PERICARP AND INTEGUMENT OF JOHNSON GRASS SEED IN RELATION TO ITS PHYSIOLOGY 1 By GEORGE T. HARRINGTON, formerly Scientific Assistant, Seed-Testing Laboratories, and WILLIAM CROCKER, formerly Plant Physiologist, Drug Plant, Poisonous Plant, Physiological and Fermentation Investigations, Bureau of Plant Industry, United States Department of Agriculture. INTRODUCTION These investigations were undertaken in hope of explaining some fea- tures of the behavior of Johnson grass seeds during their initial dormancy, their period of after-ripening, and their germination. As has been shown elsewhere (15) ,2 Johnson grass seeds belong to that group whose well- matured embryos are never'appreciably dormant, the dormancy of the intact fruit being imposed by its outer, nonliving structures. These include (1) the closely adhering, hard, brittle scales, (2) the fused pericarp and inner integument. Removal of the former hastens the germination and increases the germination capacity of the caryopses, whether these are freshly gathered, are fully after-ripened, or are in process of after- ripening, but does not appreciably affect the rate of after-ripening. Furthermore, removal of the fused pericarp and integument by corrosion with concentrated sulphuric acid or even its removal over one side of the embryo by means of a sharp needle induces the complete germination within three or four days even of freshly gathered grains which, without such treatment, would scarcely germinate at all in weeks or months. It has also been shown (15, 16) that the germination of Johnson grass seeds is highly dependent upon the maintenance of alternating temper- atures, that this sensitiveness to temperature conditions disappears upon the removal of the seed coverings, and that certain chemical substances exert a stimulating action upon their germination, particularly after the removal of the caryopses from the inclosing scales. -
Strawberry Plant Structure and Growth Habit E
Strawberry Plant Structure and Growth Habit E. Barclay Poling Professor Emeritus, NC State University Campus Box 7609, Raleigh NC 27695-7609 Introduction The strawberry plant has a short thickened stem (called a “crown”) which has a growing point at the upper end and which forms roots at its base (Fig. 1). New leaves and flower clusters emerge from “fleshy buds” in the crown in the early spring. From a cultural viewpoint, it is desirable in our region to have the formation of 1-2 “side stems” called branch crowns form during the late fall (Fig. 2). Each branch crown will add to the yield of the main crown by producing its own “flower cluster” or what is technically called an inflorescence. Branch crowns and main crowns are structurally identical, and an inflorescence develops at the terminal growing point of each crown (Fig. 3). Crown growth and development occur when temperatures are above 50o F (mainly in the month of October). Average daily temperatures in November below this temperature will slow branch crown formation and floral development. Row covers may be a good option in November for Camarosa to help stimulate further reproductive development. A well-balanced Camarosa strawberry plant will form 3-5 branch crowns by the time fruiting season begins in the spring. There is excellent potential for a 2 + lb crop per plant (> 15 tons per acre) when you can see the formation of 1-2 side crowns in addition to the main crown (center) in late fall/early winter (Fig. 7). In Chandler and Camarosa it is critical not to plant too early in the fall and run the risk of having too many crowns form (try to avoid the development of more than 6 crowns per plant). -
TYPES of FRUITS Botanically, a Fruit Develops from a Ripe Ovary Or Any Floral Parts on the Basis of Floral Parts They Develop, Fruits May Be True Or False
TYPES OF FRUITS Botanically, a fruit develops from a ripe ovary or any floral parts on the basis of floral parts they develop, fruits may be true or false. True Fruits: A true fruit or eucarp is a mature or ripened ovary, developed after fertilization, e.g., Mango, Maize, Grape etc. False Fruits: A false fruit or pseudo-carp is derived from the floral parts other than ovary, e.g., peduncle in cashew-nut, thalamus in apple, pear, gourd and cucumber; fused perianth in mulberry and calyx in Dillenia. Jack fruit and pine apple are also false fruits as they develop from the entire inflorescence. False fruits are also called spurious or accessory fruits. Parthenocarpic fruits: These are seedless fruits that are formed without fertilization, e.g., Banana. Now a day many seedless grapes, oranges and water melones are being developed by horticulturists. Pomology is a branch of horticulture that deals with Types of Fruits: A fruit consists of pericarp and seeds. Seeds are fertilized and ripened ovules. The pericarp develops from the ovary wall and may be dry or fleshy. When fleshy, pericarp is differentiated into outer epicarp, middle mesocarp and inner endocarp. On the basis of the above mentioned features, fruits are usually classified into three main groups: (1) Simple, (2) Aggregate and (3) Composite or Multiple fruits. 1. Simple Fruits: When a single fruit develops from a single ovary of a single flower, it is called a simple fruit. The ovary may belong to a monocarpellary simple gynoecium or to a polycarpellary syncarpous gynoecium. There are two categories of simple fruits—dry and fleshy.