The differences between cycads and ginkgo. Introduction: In plants, the male gamete fuses with the female gamete to produce seed. Seeds are the ones that develop into a whole new plant. Based upon the type of seeds produced, the plants are categorized into two types: gymnosperms and angiosperms. Cycad and ginkgo are types of gymnosperms.

Question

Outline a method for using apomixis to maintain feminized CannabisAssume apomixis is controlled by a single dominant gene. You can choose the type of apomixis: obligate or facultative, gametophytic or sporophytic. Discuss advantages and disadvantages of your proposed method.

Answer 1

Question

Chapter 28.2, Problem 4C

Summary Introduction

To explain: The differences between cycads and ginkgo.

Introduction: In plants, the male gamete fuses with the female gamete to produce seed. Seeds are the ones that develop into a whole new plant. Based upon the type of seeds produced, the plants are categorized into two types: gymnosperms and angiosperms. Cycad and ginkgo are types of gymnosperms.

Summary Introduction

To explain: The differences between cycads and gnetophytes.

Introduction: In plants, the male gamete fuses with the female gamete to produce seed. Seeds are the ones that develop into a whole new plant. Based upon the type of seeds produced, the plants are categorized into two types: gymnosperms and angiosperms. Cycad and gnetophytes are types of gymnosperms.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

Outline a method for using apomixis to maintain feminized CannabisAssume apomixis is controlled by a single dominant gene. You can choose the type of apomixis: obligate or facultative, gametophytic or sporophytic. Discuss advantages and disadvantages of your proposed method.

Kinetics: One-Compartment First-Order Absorption 1. In vivo testing provides valuable insight into a drug’s kinetics. Assessing drug kinetics following multiple routes of administration provides greater insight than a single route of administration alone. The following data was collected in 250-g rats following bolus IV, oral (PO), and intraperitoneal (ip) administration. Using this data and set of graphs, determine:(calculate for each variable) (a) k, C0, V, and AUC* for the bolus iv data (b) k, ka, B1, and AUC* for the po data c) k, ka, B1, and AUC* for the ip data (d) relative bioavailability for po vs ip, Fpo/Fip (e)absolute ip bioavailability, Fip (f) absolute po bioavailability, Fpo

3. A promising new drug is being evaluated in human trials. Based on preliminary human tests, this drug is most effective when plasma levels exceed 30 mg/L. Measurements from preliminary tests indicate the following human pharmacokinetic parameter values: t1/2,elim = 4.6hr, t1/2,abs = 0.34hr, VD = 0.29 L/kg, Foral = 72%. Based on these parameters, estimate the following if a 49 kg woman were to receive a 1000mg oral dose of this drug: (a) Estimate the plasma concentration of the drug at 1hr, 6 hr, and 20hr after taking the drug ( Concentration estimate) (b) Estimate the time for maximum plasma concentration (tmax). (c) Estimate the maximum plasma concentration (Cmax). (d) Estimate the time at which the plasma level first rises above 30 mg/L. (Note this is a trial and error problem where you must guess a time, plug it into the concentration equation, and determine if it is close to 30 mg/L. Hint: based on part (a) it should be apparent that the answer is less than 1hr.) (e)…